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NQ
< A >
Na
Ref.
Archean Yilgarn craton Total Western Shield
37 _+6 49_+ 13
15 37
2.6_+2.1
12
(1) (2)
Proterozoic Gawler craton Total Central Shield
82 + 24 7 8 _ 19
6 75
3.6+ 1.9
38
(1) (2)
103
face rocks and hence does not provide evidence for mantle heat flow differences beneath the two Shield regions. Unfortunately, there are no detailed models of crustal composition for both regions which would allow estimates of the mantle heat flow. However, from an analysis of the relationship between heat flow and surface heat production, Sass and Lachenbruch (1979) found that the two Shield regions are characterized by the same 'reduced' heat flow and hence concluded that differences are limited to the upper crust. The third fact is that heat flow in Australia does not conform to a simple concentric distribution away from the center of the continent: the Central Shield has higher heat flows that the Western Shield at the edge. Taken as a whole, the Australian data demonstrate that heat flow differences are accounted for by differences of crustal heat production and follow the geological assemblage. 5.2. Indian Shield A significant number of heat flow measurements are available in the Southern Indian Shield (Gupta et al., 1991, 1993). The Archean Dharwar craton can be divided in two geologically distinct regions in the East and in the West. The former has numerous granitic bodies intruding gneisses and the latter is mostly made of supracrustal granite-greenstone belts. This difference is reflected in the values of heat flow, which average to 40 _+ 3 mW m -2 and 31 _+ 4 mW m - 2 in the Eastern and Western Dharwar cratons, respectively (Gupta et al., 1991). There again, one sees that the Archean continental crust is a heterogeneous assemblage whose composition varies from one region to the next. The heat flow differences between the two parts of the craton are due to different rates of crustal heat production and do not imply deep-seated thermal contrasts. The Proterozoic Bastar craton in the central Indian Shield has larger heat flow values than its Archean counterparts. Three reliable measurements range from 51 to 64 mW m -2 (Gupta et al., 1993). These heat flow values are found through rocks with larger values of radiogenic heat production than in the Archean. For this reason, Gupta et al. (1993) conclude that the contrast in surface heat flow between the Archean and Proterozoic cratons of India is due to different upper crustal compositions.
C. Jaupart, J. C. Mareschal / Lithos 48 (1999) 93-114
104
In India, therefore, heat flow is mostly sensitive to crustal composition and its distribution does not conform to any simple geometric pattern.
5.3. East China Shield East China has been subjected to recent thermal events in the Late Mesozoic and Cenozoic implying that measured heat flow values are not in secular equilibrium with crustal heat production and mantle heat flow. Gao et al. (1998a,b) have reported a large data set for U, Th and K concentrations in rocks of all types and all metamorphic grades from the East China Shield. They present a series of detailed crustal models for various regions of East China and derive estimates of the bulk crustal heat production. One important conclusion is that crustal structure and thickness vary laterally by large amounts, implying that a single thermal model cannot account for the geological complexity of East China.
6. Mantle provinces
heat
flow
beneath
Precambrian
The detailed studies in Canada and South Africa demonstrate that large heat flow differences exist within a single province, related to differences of crustal structure. Crustal columns in different areas may vary in thickness and in composition. For example, the western part of the Abitibi Belt of Canada has a large thickness of granodioritic/tonalitic rocks and a shallow greenstone cover, and heat flows as large as 59 mW m -2. In contrast, the eastern part of the Abitibi has a thick greenstone sequence and fewer granodioritic/tonalitic plutons, which is reflected in small heat flows of about 29 mW m -2. In the Kapuskasing uplift, granulite facies terranes have been brought to the surface by low-angle thrusts and make the bulk of the crustal column. A heat flow average through this area of the Canadian Shield therefore mixes different types of crustal structure and rocks, and does not correspond to any well-defined petrological crust. Similar conclusions have been reached for the other Precambrian shields.
6.1. The crustal contribution to the surface heat flow The amount of mafic rocks in the deep crust is a key variable because it affects the crustal heat production estimate and reflects the extent of past melting events in the mantle. It has a strong effect on the average seismic velocity of the lower crust and hence may be estimated with seismological techniques (Christensen and Mooney, 1995; Rudnick and Fountain, 1995). For the purposes of estimating the crustal contribution to the surface heat flow, unfortunately, such knowledge is not sufficient. The lower crust may contain substantial amounts of felsic and enriched rocks, such as granulite-facies metapelites, for example, which have highly variable trace-element compositions and hence highly variable heat production rates (Rudnick and Fountain, 1995). Thus, it is not possible to relate heat production to seismic velocity (Fountain, 1986), and it is essential to determine the local values of heat production of each crustal structural level in each province. These problems have been discussed at length in Jaupart et al. (1998). Here, we briefly recapitulate some recent data which emphasize that the lower crust is not depleted in radioactive elements and contributes a significant amount of heat. Gao et al. (1998a,b) have derived a series of petrological and seismological models for the crust in the East China Shield. There, the lowermost crust is slightly more evolved, and slightly more radiogenic, than the average Precambrian crustal models of Rudnick et al. (1998) and Christensen and Mooney (1995). In the East China Shield, for an average thickness of 37 km, the total amount of crustal heat is 37 mW m -2, i.e., the average crustal heat production is 1.0 txW m -3. In the Indian Shield models of Gupta et al. (1991), the total Archean crustal heat flow contribution is between 26 and 21 mW m -2 for 38-km thick crust. This constrains the average Archean crustal heat production in India to be between 0.55 and 0.68 txW m -3. On average, the Archean crust beneath the Witwatersrand in South Africa has a heat production rate of 0.94 txW m -3. These independent analyses suggest that there is no such thing as a single representative Archean crustal composition. They further suggest that differences of crustal composition may account for observed heat flow variations.
C. Jaupart, J.C. Mareschal / Lithos 48 (1999) 93-114
The Witwatersrand heat flow and a crustal model based on exposures in the Vredefort structure lead to a mantle heat flow value of 17 mW m -2 for the Kaapvaal craton (Jones, 1988). With a similar procedure, Gupta et al. (1991) arrived at a range of 12-17 mW m -2 for the mantle heat flow in the Indian Shield. The difference between these estimates, = 5 mW m-2, is within the expected error range for heat flow and bulk crustal heat production.
6.2. Local studies in the Canadian Shield The mantle heat flow is a small residual value, and hence is sensitive to even small errors on the crustal heat production estimates. In the Canadian Shield, U, Th and K concentrations have been determined in all types of crustal rocks. In addition, various crustal levels can be sampled allowing reconstruction of crustal columns below and around measurement sites. The upper and middle crust have been studied over vast areas through systematic sampling (Eade and Fahrig, 1971; Shaw et al., 1986). Using geological maps, data from Ashwal et al. (1987), Fountain et al. (1987), as well as many other published reports, Pinet and Jaupart (1987) and Pinet et al. (1991) have determined the areas for each rock-type and calculated an area-weighted average in two well-sampled different granulite-facies terrains (the Kapuskasing and Pikwitonei areas) and three different amphibolite-facies terrains from the Superior Province. For the granulites, they found the same average heat production value of 0.40 txW m -3. For the three amphibolite-facies terrains, average heat production values are between 1.0 and 1.2 txW m -3. These different data sets are consistent, and come from regions directly relevant to the available heat flow data. Pinet et al. (1991) and Guillou et al. (1994, Guillou-Frottier et al. (1995) have looked in great detail at the relationship between heat flow and local crustal structure in the Archean Abitibi subprovince and its boundaries with the Kapuskasing structural zone. Heat flow increases systematically from the Grenville front to the Kapuskasing uplift over a distance of = 500 km. There is also a sharp drop of about 20 mW m -2 over a distance of 70 km across the Ivanhoe Lake fault, which separates the Abitibi from the Kapuskasing uplift. This demonstrates that
105
these variations of heat flow are of crustal origin (Fig. 2). The long wavelength variation in heat flow is accompanied by an increase in Bouguer gravity. Taken together with seismic results, these two data sets provide constraints that restrict crustal models and the mantle heat flow to a very narrow range. In the Abitibi subprovince, three crustal lithologies dominate: greenstones, tonalite-trondjemite-granodiorite (TTG) and granulite facies rocks. Large outcrops of these three lithologies are exposed in the Shield, allowing direct measurements of their densities and heat production rates. Guillou et al. (1994) generated a series of crustal models by varying the mantle heat flow, the thicknesses of the three lithological units, their densities and heat production rates. These variables are varied within rather large ranges to allow for local departures from the regional average values. Furthermore, a crustal model is considered acceptable if it generates a heat flow value within 10% of the measured value. With this procedure, data uncertainties are taken into account. The constraints of both gravity and heat flow data can be met only when the mantle heat flow lies between 7 and 15 mW m -2. The most probable value is 13 mV~r m -2"
Independent studies in large areas of low heat flow over depleted crust in the Superior and Grenville lead to estimates between 10 and 13 mW m-2 (Pinet et al., 1991; Mareschal et al., submitted). These arguments rule out values smaller than 10 mW m-2, and lead to a range of 10 to 15 mW m -2 for the mantle heat flow beneath the Canadian Shield.
7. Thermal structure and thickness of the lithosphere
7.1. The base of the lithosphere The base of the lithosphere cannot be defined without a specific model for heat transport processes (Fig. 6). There must be a boundary layer through which heat is brought from the convecting mantle into the lithosphere. Below this convective boundary layer, lateral temperature variations are small. Temperature is a continuous variable and hence global geophysical techniques, such as seismic tomography, are only able to determine the sum of the conductive
106
C. Jaupart, J.C. Mareschal/Lithos 48 (1999) 93-114
0
Tm
Temperature
~.~,
Conductive boundary layer
Boundary layer
Convecting mantle
Fig. 6. Sketch illustrating various definitions of lithospheric thickness, h 1 corresponds to the stable part of the lithosphere, where heat transport is achieved by conduction, h 2 is obtained by downward continuation of temperature to an isentropic temperature profile representative of the fully convecting mantle, h 3 is the total thickness over which temperature contrasts with the surrounding oceanic mantle persist. Large-scale tomographic images allow estimates of h 3.
layer and the boundary layer below it, down to a depth which we shall note h 3 (Fig. 6). In order to make a quantitative comparison between the different thickness estimates, one must specify the structure of the convective boundary layer. One possibility if that this boundary layer is unstable and generates small-scale convective motions (Parsons and McKenzie, 1978; Davaille and Jaupart, 1994; Doin et al., 1997). Another possibility is that it is stable and develops as continents sweep over the convecting mantle (Gurnis, 1988; Lenardic and Kaula, 1995; Lenardic and Kaula, 1996). Questions about the long-term survival of the lithosphere, geochemical reservoirs isolated from the fully convecting mantle and transient thermal effects in the lithosphere, deal with the conductive layer which has thickness h 1 (Fig. 6). This is only part of the total thermal boundary layer, and h 1 < h 3. Finally, one must introduce a third thickness value, h2, c o r r e s p o n d i n g to the value obtained by downward continuation of temperature to an isentropic 'oceanic' profile. As shown in Fig. 6, this leads to an intermediate value of the lithosphere thickness, i.e., one has h 1 < h 2 _< h 3. By requiring that the base of the lithosphere lies along a well-mixed isentropic 'oceanic' tempera-
ture profile, one makes the additional assumption that mantle temperatures below continents are the same than beneath oceans, which may not be valid, as shown by dynamical simulations of the effect of continents at Earth's surface (Gurnis, 1988; GuillouFrottier et al., 1995; Moresi and Lenardic, 1997). This effect, however, is expected to be small. The main point is that the 'cold roots' of seismic tomography must extend deeper than both h~ and h2, i.e., the thicknesses which may be derived from thermal considerations. In the convective boundary layer at the bottom of the lithosphere, temperature tends asymptotically to the fully convective profile. Thus, an additional definition is required to calculate the thickness of this layer. In some calculations, the base of this layer is such that temperature reaches a prescribed percentage of the fully convecting mantle temperature. In another definition, the conduction profile is extrapolated linearly until it meets the convecting mantle temperature. This second procedure is analogous to the one used to calculate h2, and hence the convective boundary layer thickness is equal to the difference between h 2 and h~. Jaupart et al. (1998) have recently investigated the small-scale convection
C. Jaupart, J.C. Mareschal/ Lithos 48 (1999) 93-114
model using likely values of mantle rheological parameters and have found a value of 40 km for this thickness difference.
7.2. Vertical temperature profiles We compare changes of deep lithospheric structure across the Abitibi Province with an average thermal model for the younger Appalachian Province. The western part of the Abitibi is characterized by heat flows that are large by Archean standards (59 mW m -z) and contrasts with the eastern Abitibi which has some of the lowest heat flow values found in the Shield (28 mW m-Z). The Appalachians are associated with a high average heat flow of 57 mW m -2, due to a relatively thin enriched upper crustal layer (Jaupart et al., 1982). We have calculated geotherms for different areas using constraints from heat flow data and models for the distribution of heat production in the crust (Table 5). The crustal model has a maximum of three layers with different heat production values. In most calculations, the deepest layer has a heat production of 0.40 IxW m -3, corresponding to granulite-facies terranes in Canada and in the Norwegian Shield. The latter comes from studies in the Egersund-Bamble area of southern Norway (Pinet and Jaupart, 1987), which was one part of the same geological province than the Grenville and hence provides a window into Grenvillian lower crust. The Shield crustal models have
Table 5 Thermal models for eastern Canada WA1 and WA2 are the West Abitibi models. EA is East Abitibi, and Appl and App2 are the Appalachian models. WA1 Qs (mW m -2 ) db a~ db A~ db a~ Crustal
Tr~ (~
52 41 0.98 -
thickness (km)
41 523
WA2 52 30 1.2 11 0.4 -
41 472
a Temperature at the Moho. bLayer thickness (km). c Heat production in layer (txW m - 3 ).
EA 28 20 0.2 28 0.4 -
48 385
Appl
App2
58 8 3.1 10 1.1 22
58 8 2.5 32 0.8
0.4
40 402
-
40 477
107
been discussed above (Pinet et al., 1991; GuillouFrottier et al., 1995). In the Appalachians, heat flow and gravity data demonstrate that surface heat production rates do not extend deeper than a few kilometres (Jaupart et al., 1982; Jaupart, 1983). We first neglect heat production in the mantle part of the lithosphere, which leads to lower bounds for the lithosphere thickness h 2 (Fig. 6). Over the large horizontal distances which separate the regions of Table 4, lateral heat transfer is inefficient and thermal differences extend over great vertical distances, from the surface to the base of the lithosphere. In western Abitibi, heat flow increases toward the edge of the province, toward the Kapuskasing uplift, with a very large wavelength. However, it drops to a small value over a short wavelength on the uplift itself. One must expect some horizontal heat transport in this area. The highest western Abitibi heat flow is 59 mW m -2 and we use a regional average of 52 mW m-2 for this part of the Superior Province. In the crust, thermal conductivity is fixed at 2.5 W m -1 K -1. For the mantle, we account for both lattice conduction and radiation and take the following equation:
k ( T ) = 0.174 + 0.000265T
+
0.368
10 - 9 T 3
(3)
where T is the absolute temperature. This takes into account measurements from several laboratories (Schatz and Simmons, 1972; Beck et al., 1978; Sch~irmeli, 1979), and gives conductivity values which are slightly smaller than those of Schatz and Simmons (1972) at temperatures below 1200 K. Following our analysis, the Moho heat flow is taken to be 12 mW m -2. The crustal models and the resulting Moho temperatures are summarized in Table 5. One source of uncertainty is the vertical distribution of crustal heat production. Different crustal models for the same total heat production indicate that Moho temperature estimates may be inaccurate by several tens of degrees (Table 5). Moho temperatures are coldest beneath the East Abitibi (385~ and highest (523~ in the West Abitibi area. Moho temperatures beneath the young Appalachian Province may be slightly smaller than those beneath the much older Abitibi. Fig. 7 shows the two extreme geotherms through the
108
C. Jaupart, J.C. Mareschal / Lithos 48 (1999) 93-114
Temperature (C) ,~-.. \ .. \'.. \ \ \ \ \ \ \ \ \
..~ -125
\ \
\
",. '..
\ \
".. \
'. \
_ _ _ East Abitibi
........ West Abitibi
9 \ \
".. '.. \
".. \
.. \
Isentropic profile
independent data such as (P,T) estimates from mantle nodule compositions or the diamond stability field because of uncertainties in the values of thermal conductivity and heat production in mantle rocks. The former source of uncertainty is due in part to the rather small number of carefully conducted measurements and in part to a problem of a more fundamental nature. In the mantle, crystal dimensions are close to the photon mean free path (Schatz and Simmons, 1972; Nicolas and Poirier, 1976). Scattering at grain boundaries is the dominant effect and limits the efficacy of radiative heat transport. A proper determination of bulk mantle conductivity must therefore take into account crystal shapes, sizes and orientations.
9
7.3. Heat production in a thick lithosphere
\ \
-300 Fig. 7. Highest and lowest geotherms for eastern Canada. Geotherms for the Grenville Province and for the Appalachians would fit between these two extreme values (see Table 5).
whole lithosphere. We arbitrarily define the base of the lithosphere to be at well-mixed convective mantle temperatures, along an isentropic profile with a potential temperature of 1280~ (McKenzie and Bickle, 1988). With these definitions, the lithosphere extends to depths of about 290 and 250 km under the coldest and hottest parts of the Abitibi subprovince. Thus, significant differences of deep lithospheric structure are predicted away from known geological boundaries. These estimates of lithosphere thickness h 2 c o r r e s p o n d to a mantle heat flow of 12 mW m -2, which is our best estimate. However, mantle heat flow values of up to 15 mW m-2 are not ruled out by the data, and would lead to decrease the thickness estimates by about 50 km. In the Kaapvaal craton, the 18 mW m -2 variation in surface heat flow imply a difference in Moho temperature of = 125 K between the Witwatersrand and the neighboring regions. These calculations allow a comparison between different provinces for a given set of assumptions on thermal conditions and thermal properties. However, they must be used with caution for comparisons with
In order to avoid deep temperature extrapolations and uncertainties in the values of thermal conductivity, one may use constraints on the mantle heat flow value and estimates of heat production in the cratonic mantle. If the continental lithosphere is very thick, as advocated by Jordan (1981), for example, the thermal time-constant is very large and one must expect a significant component of heat flow due to transient effects. One transient effect which has not been studied is that of radiogenic heat production. If the mantle part of the lithosphere contains a non-negligible amount of U, Th and K, one must account for the rundown of radioactivity with time. The time-constant of the decay of bulk radiogenic heat production depends on the relative amounts of the four isotopes, 238U and 235Th, 232Uand 4~ which have different half-lives. For 'average' T h / U and K / U ratios, the bulk heat production decreases by a factor of about 3 in 3 billion years. One may approximate the heat production by an exponential function: A ( t ) = A 0 e x p ( - at). The characteristic thermal relaxation time of the lithosphere is r = if~K, where L is the thickness of the lithosphere and K is the thermal diffusivity. Here L corresponds to thickness h~ in Fig. 6. It is shown in Appendix B that the contribution of the lithospheric heat production to the surface heat flow is: tan~a~
AQ(t) =AL
v/aT e x p ( - t~t).
(4)
C. Jaupart, J.C. Mareschal / Lithos 48 (1999) 93-114
This is compared to the instantaneous amount of heat produced in the lithosphere: AQ0 ( t ) = AL exp( - cet).
(5)
The ratio between these two quantities gives the magnitude of the time-delay effect: 2~Q ( t )
tan f~-r =
(6)
AOo( t)
'
which is an increasing function of lithosphere thickness. The ratio reaches a value of 1.5 for a 300-km thick lithosphere. This shows that surficial heat flow measurements record some time-average of deep heat production and are not in equilibrium with the instantaneous lithospheric heat production. Fig. 8 shows the contribution of radiogenic elements in the lithosphere to the surface heat flow. It is useful to compare this with the heat flow which is conducted through the lithosphere in steady state. For the sake of argument, we consider the simplest case of a lithosphere lying on top of a mell-mixed mantle with a uniform temperature of 1573 K. The conducted heat flow is then
Qc=k
AT (7)
h '
where A T = 1300 K, h stands for the lithosphere thickness and the value of k has been fixed at 3.0 W m -1 K -1. It may be seen that, for all values of
40
_
r
30
'
~
,,
_
!
on
'
/
', lithosphere /f ',,!approximate/)/
20
1/I
'
/
/ /
//
_
<
'
/
10 Z 9 r
0
100
2oo
300
400
LITHOSPHERE THICKNESS (km) Fig. 8. Contribution of heat production in the mantle lithosphere to the present surface heat flow. Numbers along the curves stand for values of heat production (~zW m-3). The dashed curve corresponds to steady-state conduction over a temperature difference of 1300 K, for a thermal conductivity of 3.0 W m-1 K-1
109
mantle heat production A larger than 0.02 IxW m -3, the radioactive contribution is comparable to the conducted heat flux in lithospheres thicker than 200 km (Fig. 8). In a 300-km thick lithosphere, mantle heat production must be smaller than 0.01 IxW m -3 to contribute less than 5 mW m -z. Rudnick et al. (1998) have recently compiled measurements of U, Th and K concentrations in different types of upper mantle samples and have found a large range of heat production rates. The lowest values belong to large fragments of the upper mantle which have been brought to the surface by tectonic processes ('massif' peridotites). Rudnick et al. (1998) favor data from peridotite xenoliths found in alkali basalts, and propose a cratonic mantle heat production of 0.02 txW m -3. For comparison with heat flow constraints, one must take into account heat conduction along an isentropic profile, which contributes a heat flux of about 2 mW m -2. Thus, using our constraints on the mantle heat flow value, the maximum amount of heat produced in the Canadian lithosphere is between 8 and 13 mW m -2. A cratonic heat production of 0.02 IxW m -3 rules out lithosphere thicknesses larger than 330 km. For thicknesses larger than 300 km, the time-constant for thermal diffusion in the lithosphere is comparable to, and may even be larger than, the age of geological provinces in the Canadian Shield. In such conditions, surficial heat flow records an additional transient associated with relaxation of the thermal structure achieved at the end of the last tectonic or magmatic event. This argument shows that very thick lithospheres ( > 400 km) can be ruled out if radiogenic heat production in the mantle part of the lithosphere is as large as suggested by Rudnick et al. (1998), independently of uncertainties in the values of thermal conductivity. Partial melting, required to stabilize a deep and cold lithospheric root (Jordan, 1981; Doin et al., 1997), also leads to the depletion of incompatible elements such as U, Th and K. If the 'massif' peridotites offer representative samples of the cratonic mantle, heat production in the deep lithosphere may be as small as 0.006 IxW m -3 (Rudnick et al., 1998). In this case, heat production does not allow useful constraints on lithosphere thickness and the temperature profiles of Fig. 7 are a reasonable approximation. A key question is whether depletion
110
C. Jaupart, J.C. Mareschal / Lithos 48 (1999) 93-114
processes have affected the Canadian and South African lithospheres with the same intensity. The difference between the mantle heat flow estimates for the two shields may well be due to differences of cratonic mantle heat production. 7. 4. Discussion
Continents are not immobile at Earth's surface and it is unlikely that thermal conditions at their base can be kept constant for long times. For a stable lithosphere thickness h I equal to 250 km and a thermal diffusivity of 10 -6 m 2 s - l , it may be shown that surface heat flow does not record changes of basal conditions over periods smaller than 1 Ga. Thus, there may be no relationship between the present-day deep mantle circulation and continental heat flow. Heat flow measurements allow constraints on the stable and conductive part of the lithosphere. For the convecting mantle, however, it is the whole thermal boundary layer which matters (the 'thermal' lithosphere) and this cannot be defined without consideration of the dynamical interactions between a thick root and the surrounding mantle. The key point is that continents cannot be treated as passive. In this paper, we have shown that one must allow for thermal differences imposed from the top down: known contrasts in crustal heat production lead to significant differences of deep thermal structure which may play an important role for mantle convection.
8. Conclusions (1) Interpretations of continental heat flow data often refer to the linear heat flow-heat production relationship. In the Canadian Shield, this concept is not very useful. All the data from the different provinces in the eastern Canadian Shield fit equally well (or, to be more accurate, equally poorly) the same heat flow-heat production relationship. (2) Geographic variations of the heat flow are found within Precambrian provinces. These variations reflect changes in crustal heat production. Because these variations are very often systematic and related to large-scale changes of crustal structure, an
average value of heat flow is difficult to compare with a synthetic crustal model derived from petrological or chemical considerations. (3) The heat flow is significantly higher in the Proterozoic provinces of South Africa than in those of North America. The apparent relationship between heat flow and crustal age, obtained from worldwide averaging of the heat flow values from provinces of the same age, does not hold when different provinces of the same continents are compared. (4) In Canada and in South Africa, large amplitude (-- 40 mW m -z ) heat flow variations are found over short distances. Such variations can only have a crustal source. In Canada, there is no detectable variation in mantle heat flow between provinces of the Shield. In South Africa, a difference in mantle heat flow between adjacent Proterozoic and Archean provinces is not required by the data. (5) The estimated values of mantle heat flow (10-15 mW m - 2 in Canada and 17 mW m - 2 in the Kaapvaal craton) yield constraints on lithospheric thickness and heat production in the mantle lithosphere. Lithosphere thicknesses larger than 330 km are inconsistent with heat production measurements in mantle xenoliths from South Africa. Thicknesses smaller than 200 km are not consistent with the mantle heat flow values. (6) Different geophysical interpretations do not rely on the same definition of lithosphere thickness. (7) Deep temperature extrapolations may be inaccurate due to uncertainties in thermal conductivity in the cratonic mantle. Determination of the base of the lithosphere requires knowledge of the mechanism of heat transport into the lithosphere. One may choose to emphasize these difficulties, but a more optimistic conclusion is that, despite these potential problems, it is now possible to focus on a specific range of thickness estimates. One may anticipate that even slight improvement on a single variable will considerably tighten the range.
Appendix A. Accuracy of heat flow determinations Heat flow values are determined in the field, in imperfectly controlled environments. Errors do not arise from intrinsic instrumental problems, but from
C. Jaupart, J.C. Mareschal / Lithos 48 (1999)93-114
geological and climatic noise. Because heat flow and temperature profiles are compared to independent data, it is useful to recapitulate the key steps in the measurement technique and the errors involved. In principle, all problems could be avoided if very deep boreholes (deeper than -- 12000 m) could be used. This is seldom the case and there are several types of difficulties. (1) One problem is that rocks may be permeable at shallow depths and interstitial water may transport a significant amount of heat which goes undetected. At large depths, fractures and most pores close due because of high confining pressure, and permeability tends to very small values. (2) Noise can be introduced by variations of the boundary condition at the surface. Effects of topography and lakes can easily be detected and accounted for. More subtle changes, such as due to the effect of the vegetation on the ground surface temperature, can remain undected. When the temperature gradient is small, as often in the Canadian Shield, these perturbations of the gradient can exceed 10% near the surface. They are more easily detected and eliminatedwhen measurements are available from several boreholes. (3) The third type of problems may arise because of lateral heat transfer, due for example to heat refraction in a borehole located near the boundary between rocks with different values of conductivity. When the borehole extends through a narrow body with a strong contrast in conductivity, the local enhancement of the heat flow can be as large as 50% (Guillou-Frottier et al., 1996). Refraction effects are difficult to account for without complete knowledge of the subsurface structure, and the best procedure is to assess directly the magnitude of lateral heat transfer by temperature measurements. One method is to verify that throughout the depth range of the borehole, the local value of the vertical heat flow at each depth is the same. Refraction effect can also be detected when several nearby boreholes are available. Their common value is then assigned to the site. (4) One of the main difficulties lies in estimating the thermal conductivity. Good quality conductivity measurements are made with the 'divided bar' technique. In order to detect local 'grain' effects due to heterogeneity in rock composition, measurements are
111
made on cylinders of different thicknesses. The bulk thermal conductivity value must not depend on sample thickness. These measurements are time consuming because they must be made in thermal equilibrium. Because of the limited number of core samples that can be measured, it is important to sample properly the lithologies in the borehole and to eliminate unrepresentative samples. Poor sampling can result in ~ 20% error on the estimated heat flow. (5) Climatic variability has caused changes in the boundary condition at Earth's surface. Such perturbations propagate slowly through rock and induce a thermal transient at depth. The magnitude of these transients decreases with depth and eventually becomes negligible. For very recent climatic changes (the past 200 years), temperature perturbations are negligible below ~ 200 m. Pleistocene climatic effects extend over more than 3 km, and most boreholes are shallower than this. Sass and Lachenbruch (1979) analyzed temperature data from a very deep borehole in the Proterozoic Flin Flon Belt and found no evidence for Pleistocene effects. Unfortunately, their study did not provide a definite answer because of uncertainties in the conductivity data. The practice has been to make an adjustment for glacial-interglacial climate variability only on heat flow data from regions that were covered by glaciers, although it is now clear that temperature were affected throughout the northern hemisphere. The standard procedure is thus to make a correction based on a model of Pleistocene climate variations (Jessop, 1971). In the Canadian Shield, heat flow and temperature gradients are low and hence the correction is small, typically 2 - 3 mW m -2. The relative error on the magnitude of this correction may be large, but the resulting error on the heat flow is small and within the range of measurement uncertainty. However, the correction is systematic and increases the heat flow value. Pleistocene glaciation was most prominent in the northern hemisphere and should not affect temperatures in the southern hemisphere. Indeed, uncorrected heat flow values seem to be systematically higher in the southern hemisphere than in the northern hemisphere (Sclater et al., 1981). These differences disappear when the northern hemisphere data are corrected. Heat flow values from South Africa have not been corrected for Pleistocene climatic effects.
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Appendix B. Heat sources in the lithosphere
References
In order to calculate the effect on the heat flow of the rundown of the heat sources in the mantle lithosphere, we solve the heat equation:
Arshavsakaya, N.I., Galdin, N.E., Karus, E.W., Kuznetsov, O.L., Lubimova, E.A., Milanovski, S.Y., Nartikoev, V.D., Semaskko, S.A., Smirnova, E.V., 1987. Geothermic investigations. In: Kozlovsky, Y.A. (Ed.), The Superdeep Well of the Kola Peninsula. Springer-Verlag, New-York, pp. 387-393. Ashwal, L.D., Morgan, P., Kelley, S.A., Percival, J., 1987. Heat production in an Archean crustal profile and implications for heat flow and mobilization of heat producing elements. Earth Planet. Sci. Lett. 85, 439-450. Ballard, S., Pollack, H.N., Skinner, N.J., 1987. Terrestrial heat flow in Botswana and Namibia. J. Geophys. Res. 92, 62916300. Beck, A.E., Dharba, D.M., Schloessin, H.H., 1978. Lattice conductivities of single crystal and polycrystalline materials at mantle pressures and temperatures. Phys. Earth Planet. Int. 17, 35-53. Birch, F., Roy, E.R., Decker, E.R., 1968. Heat flow and thermal history in New England and New York. In: An-Zen, E. (Ed.), Studies of Appalachian Geology. Wiley (Interscience), New York, pp. 437-451. Christensen, N.I., Mooney, W.D., 1995. Seismic velocity structure and composition of the continental crust: a global view. J. Geophys. Res. 100, 9761-9788. Clauser, C., Gieses, P., Huenges, E., Kohl, T., Lehmann, H., Rybach, L., Safanda, J., Wilhelm, H., Windlow, K., Zoth, G., 1997. The thermal regime of the crystalline continental crust: implications from the KTB. J. Geophys. Res. 102, 1841718441. Clowes, R.M., Cook, F.A., Green, A.G., Keen, C.E., Ludden, J.N., Percival, J.A., Quinlan, G.M., West, G.F., 1992. LITHOPROBE New perspectives on crustal evolution. Can. J. Earth Sci. 29, 1831-1864. Cull, J.P., 1991. Heat flow and regional geophysics in Australia. In: Cermak, V., Rybach, L. (Eds.), Terrestrial Heat Flow and the Lithosphere Structure. Springer Verlag, Berlin, pp. 486500. Davaille, A., Jaupart, C., 1994. Onset of thermal convection in fluids with temperature dependent viscosity: application to the oceanic mantle. J. Geophys. Res. 99, 19853-19866. Doin, M.P., Fleitout, L., Christensen, U.R., 1997. Mantle convection and stability of depleted and undepleted continental lithosphere. J. Geophys. Res. 102, 2771-2788. Drury, M.J., 1985. Heat flow and heat generation in the Churchill Province of the Canadian Shield and their paleotectonic significance. Tectonophysics 115, 25-44. Drury, M.J., Taylor, A.E., 1987. Some new measurements of heat flow in the Superior Province of the Canadian Shield. Can. J. Earth Sci. 24, 1486-1489. Drury, M.J., Jessop, A.M., Lewis, T.J., 1987. The thermal nature of the Canadian Appalachians. Tectonophysics 113, 1-14. Durrheim, R.V., Green, R.W.E., 1992. A seismic refraction investigation of the Archean Kaapvaal craton, South Africa, using mine tremors as the energy source. Geophys. J. Int. 108, 812-832.
1 0T
02T
A
Ot
0Z 2
K exp'
K
(B1)
at),
where K is the thermal diffusivity, A is the heat source density, K is the thermal conductivity, and ol ~ 0 . 5 1 0 . 9 year -1. We assume that the temperature is 0 at the surface z - 0 and that the heat flow is 0 at the base of the lithosphere z - L. We shall assume that the effect of the initial conditions has been damped out and can be neglected, and a solution can be obtained by expanding the temperature in the following Fourier series:
T ( z , t ) = }7~ c~(t)sin (2k + 1 ) ~
(B2)
k=0
with 1 ~ s i n 1 = - 27 r k = 0 2 k + l
2k+l)
-~
0
The solution the temperature is obtained as: 16AL 2
r(z,t)
-
. •
"n-pC e x. p ( a t.)
. exp( 2-
k=0
(2k +
1)2 ,
2 t/4L2)
+ 1)2=2 (B4)
Neglecting the transient terms due to the poorly defined initial condition, we obtain the surface heat flow as: OT ~ 1 K - - = 8 AL exp( - c~t) E 0z ~=0 4 a t - (2k -+- 1) 277"2
(BS) aT tan~/ar K-- =AL exp( - a t ) Oz
V/c~r
with r = L2/K.
(B6)
C. Jaupart, J.C. Mareschal / Lithos 48 (1999) 93-114
Eade, K.E., Fahrig, W.F., 1971. Geochemical evolutionary trends of continental plates. A preliminary study of the Canadian Shield. Geol. Surv. Canada Bull. 179, 59. Fountain, D.M., 1986. Is there a relationship between seismic velocity and heat production for crustal rocks?. Earth Planet. Sci. Lett. 79, 145-150. Fountain, D.M., Salisbury, M.H., Furlong, K.P., 1987. Heat production and thermal conductivity of rocks from the Pikwitonei-Sachigo continental cross section, central Manitoba: implications for the thermal structure of Archean crust. Can. J. Earth Sci. 24, 1583-1594. Gao, S., Luo, T.-C., Zhang, B.-R., Zhang, H.-F., Han, Y.-W., Hu, Y.-K., Zhao, Z.-D., 1998a. Chemical composition of the continental crust as revealed by studies in East China. Geochim. Cosmochim. Acta 62, 1959-1975. Gao, S., Zhang, B.-R., Jin, Z.-M., Kern, H., Luo, T.-C., Zhao, Z.-D., 1998b. How mafic is the lower continental crust?. Earth Planet. Sci. Lett. 161, 101-117. Green, R.W.E., Durrheim, R.J., 1990. A seismic refraction investigation of the Namaqualand metamorphic complex, South Africa. J. Geophys. Res. 95, 19927-19932. Guillou, L., Mareschal, J.-C., Jaupart, C., Gari@y, C., Bienfait, G., Lapointe, R., 1994. Heat flow gravity and structure of the Abitibi belt, Superior Province, Canada: implications for mantle heat flow. Earth Planet. Sci. Lett. 122, 103-123. Guillou-Frottier, L., Mareschal, J.-C., Jaupart, C., Gari@y, C., Lapointe, R., Bienfait, G., 1995. Heat flow variations in the Grenville Province, Canada. Earth Planet. Sci. Lett. 136, 447-460. Guillou-Frottier, L., Jaupart, C., Mareschal, J.-C., Gari@y, C., Bienfait, G., Cheng, L.Z., Lapointe, R., 1996. High heat flow in the Thompson Belt of the Trans-Hudson Orogen, Canadian Shield. Geophys. Res. Lett. 23, 3027-3030. Gupta, M.L., Sundar, A., Sharma, S.R., 1991. Heat flow and heat generation in the Archean Dharwar cratons and implications for the Southern Indian Shield geotherm and lithospheric thickness. Tectonophysics 194, 107-122. Gupta, M.L., Sundar, A., Sharma, S.R., Singh, S.B., 1993. Heat flow in the Bastar craton, central Indian Shield: implications for thermal characteristics of Proterozoic cratons. Phys. Earth Planet. Int. 78, 23-31. Gurnis, M., 1988. Large-scale mantle convection and the aggregation and dispersal of supercontinents. Nature 332, 695-699. Hart, R.J., Nicolaysen, L.O., Gale, N.H., 1981. Radioelement concentrations in deep profile through Archean basement of the Vredefort structure. J. Geophys. Res. 86, 10639-10652. Hart, S.R., Steinhart, J.S., Smith, T.J., 1994. Terrestrial heat flow in Lake Superior. Can. J. Earth Sci. 31,698-708. Hoffman, P.F., 1989. Precambrian geology and tectonic history of North America. In: Bally, A.W., Palmer, E.R. (Eds.), The Geology of North America--An Overview. GSA, Boulder, CO, pp. 447-512. Jaupart, C., 1983. Horizontal heat transfer due to radioactivity contrasts: causes and consequences of the linear heat flow-heat production relationship. Geophys. J. R. Astron. Soc. 75, 411435. Jaupart, C., Mann, J.R., Simmons, G., 1982. A detailed study of
113
the distribution of heat flow and radioactivity in New Hampshire (USA). Earth Planet. Sci. Lett. 59, 267-287. Jaupart, C., Mareschal, J.-C., Guillou-Frottier, L., Davaille, A., 1998. Heat flow and thickness of the lithosphere in the Canadian Shield. J. Geophys. Res. 103, 15269-15286. Jessop, A.M., 1971. The distribution of glacial perturbation of heat flow in Canada. Can. J. Earth Sci. 8, 162-166. Jessop, A.M., Lewis, T.J., Judge, A.S., Taylor, A.E., Drury, M.J., 1984. Terrestrial heat flow in Canada. Tectonophysics 103, 239-261. Jones, M.Q.W., 1987. Heat flow and heat production in the Namaqua mobile belt, South Africa. J. Geophys. Res. 92, 6273-6289. Jones, M.Q.W., 1988. Heat flow in the Witwatersrand Basin and environs and its significance for the South African shield geotherm and lithosphere thickness. J. Geophys. Res. 93, 3243-3260. Jones, M.Q.W., 1992. Heat flow anomaly in Lesotho: implications for the southern boundary of the Kaapvaal craton. Geophys. Res. Lett. 19, 2031-2034. Jordan, T.H., 1981. Continents as a chemical boundary layer. Trans. R. Soc. (London), Ser. A 301,359-373. Lachenbruch, A.H., 1970. Crustal temperature and heat production: implications of the linear heat flow heat production relationship. J. Geophys. Res. 73, 3292-3300. Lenardic, A., Kaula, W.M., 1996. Near surface thermal/chemical boundary layer convection at infinite Prandtl number: two-dimensional numerical experiments. Geophys. J. Int. 126, 689711. Mareschal, J.-C., Pinet, C., Gari@y, C., Jaupart, C., Bienfait, G., Dalla-Coletta, G., Jolivet, J., Lapointe, R., 1989. New heat flow density and radiogenic heat production data in the Canadian Shield and the Qu6bec Appalachians. Can. J. Earth Sci. 26, 845-852. Mareschal, J.-C., Jaupart, C., Cheng, L.Z., Rolandone, F., Gariepy, C., Bienfait, G., Guillou-Frottier, L., Lapointe, R., 1999. Heat flow in the Trans-Hudson Orogen of the Canadian Shield: implications for Proterozoic continental growth, J. Geophys. Res., in press. McKenzie, D.P., Bickle, M.J., 1988. Volume and composition of melt generated by extension of the lithosphere. J. Petrol. 29, 625-679. Moresi, L.-N., Lenardic, A., 1997. Three-dimensional numerical simulations of crustal deformation and subcontinental mantle convection. Earth Planet. Sci. Lett. 150, 233-243. Morgan, P., 1985. Crustal radiogenic heat production and the selective survival of continental crust. J. Geophys. Res. 90, C561-C570. Nicolas, A., J.-P. Poirier, 1976. Crystalline Plasticity and Solid State Flow in Metamorphic Rocks. Wiley, New York. Nicolaysen, L.o., Hart, R.J., Gale, N.H., 1981. The Vredefort Radioelement Profile extended to supracrustal strata at Carletonville, with implications for continental heat flow. J. Geophys. Res. 86, 10653-10661. Nixon, P.H., Rogers, N.W., Gibson, I.L., Grey, A., 1981. Depleted and fertile mantle xenoliths from southern African kimberlites. Annu. Rev. Earth Planet. Sci. 9, 285-309.
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Nyblade, A.A., Pollack, H.N., 1993. A global analysis of heat flow from Precambrian terrains: implications for the thermal structure of Archean and Proterozoic lithosphere. J. Geophys. Res. 98, 12207-12218. Parsons, B., McKenzie, D.P., 1978. Mantle convection and the thermal structure of the plates. J. Geophys. Res. 83, 44854495. Pinet, C., Jaupart, C., 1987. The vertical distribution of radiogenic heat production in the Precambrian crust of Norway and Sweden: geothermal implications. Geophys. Res. Lett. 14, 260-263. Pinet, C., Jaupart, C., Mareschal, J.-C., Gari6py, C., Bienfait, G., Lapointe, R., 1991. Heat flow and structure of the lithosphere in the eastern canadian shield. J. Geophys. Res. 96, 1994119963. Polyak, B.G., Smirnov, Y.B., 1968. Relationship between terrestrial heat flow and tectonics of the continents. Geotectonics 4, 205-213. Qiu, X., Priestley, K., McKenzie, D., 1996. Average lithospheric structure of southern Africa. Geophys. J. Int. 127, 563-587. Rudnick, R.L., Fountain, D.M., 1995. Nature and composition of the continental crust: a lower crustal perspective. Rev. Geophys. 33, 267-309. Rudnick, R.L., McDonough, W.F., O'Connell, R.J., 1998. Thermal structure, thickness and composition of continental lithosphere. Chemical Geology 145, 395-411. Sass, J.H., A.H. Lachenbruch, 1979. Thermal regime of the Australian continental crust. In: McElhinny, M.W. (Ed.), The
Earth: its Origin, Structure and Evolution. Academic Press, New York, pp. 301-351. Sch~irmeli, G., 1979. Identification of radiative thermal conductivity in olivine up to 25 kbar and 1500 K, Proc. 6th AIRAPT Conf. In: Timmerhauf, K.D., Barber, M.S. (Eds.). Plenum, New York, pp. 60-74. Schatz, J.F., Simmons, G., 1972. Thermal conductivity of earth materials. J. Geophys. Res. 77, 6966-6983. Sclater, J.G., Parsons, B., Jaupart, C., 1981. Oceans and continents: similarities and differences in the mechanisms of heat loss. J. Geophys. Res. 86, 11535-11552. Shaw, D.M., Cramer, J.J., Higgins, M.D., Truscott, M.G., 1986. Composition of the Canadian Precambrian Shield and the continental crust of the earth. In: Dawson, J.B. et al. (Eds.), Nature of the Lower Continental Crust. Geol. Soc., London, pp. 257-282. Smithson, S.B., Decker, E.R., 1974. A continental crustal model and its geothermal implications. Earth Planet. Sci. Lett. 22, 215-225. Smithson, S.B., Ramberg, I.B., 1979. Gravity interpretation of the Egersund anorthosite complex, Norway: its petrological and geothermal significance. Bull. Geol. Soc. Am. 90, 199-204. Taylor, S.R., McLennan, S.M., 1985. The continental crust: its composition and evolution. Blackwell, Cambridge, MA, 312 pp. Vitorello, I., Pollack, H.N., 1980. On the variation of continental heat flow with age and the thermal evolution of continents. J. Geophys. Res. 85, 983-995.
LITHOS
ELSEVIER
Lithos 48 (1999) 115-133
Stability and dynamics of the continental tectosphere Steven S. Shapiro ~, Bradford H. Hager * , Thomas H. Jordan Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA Received 19 October 1998; received in revised form 8 February 1999; accepted 15 February 1999
Abstract Continental cratons overlie thick, high-viscosity, thermal and chemical boundary layers, where the chemical boundary layers are less dense than they would be due to thermal effects alone, perhaps because they are depleted in basaltic constituents. If the continental tectosphere is the same age as the overlying Archaean crust, then the continental tectosphere must be able to survive for several billion years without undergoing a convective instability, despite being both cold and thick. Since platforms and shields correlate only weakly with Earth's gravity and geoid anomalies, acceptable models of the continental tectosphere must also satisfy this gravity constraint. We investigate the long-term stability of the continental tectosphere by carrying out a number of numerical convection experiments within a two-dimensional Cartesian domain. We initiate our experiments with a tectosphere (thermal and chemical boundary layers) immersed in a region of uniform composition, temperature, and viscosity, and consider the effects on the stability of the tectosphere of (1) activation energy (used to define the temperature dependence of viscosity), (2) compositional buoyancy, and (3) linear or non-linear rheology. The large lateral thermal gradients required to match oceanic and tectosphere structures initiate the dominant instability, a "drip" which develops at the side of the tectosphere and moves to beneath its center. High activation energies and high background viscosities restrict the amount and rate of entrainment. Compositional buoyancy does not significantly change the flow pattern. Rather, compositional buoyancy slows the destruction process somewhat and reduces the stress within the tectosphere. With a non-Newtonian rheology, this reduction in stress helps to stiffen the tectosphere. In these experiments, dynamical systems that adequately model the present ocean-continent structures have activation energy E* > 180 kJ m o l e a value about one third the estimate of activation energy for olivine, E* -- 520 kJ mole-1. Although for E* ~ 520 kJ mole-1, compositional buoyancy is not required for the tectosphere to survive, the joint application of longevity and gravity constraints allows us to reject all models not containing compositional buoyancy, and to predict that the ratio of compositional to thermal buoyancy within the continental tectosphere is approximately unity. 9 1999 Published by Elsevier Science B.V. All rights reserved. Keywords: Continental tectosphere; Dynamics; Conductive cooling; Mantle convection; Mantle rheology
* Corresponding author i Now at the Department of Physics, Guilford College, Greensboro, NC 27410, USA. 0024-4937/99/$- see front matter 9 1999 Published by Elsevier Science B.V. All rights reserved. PII: S 0 0 2 4 - 4 9 3 7 ( 9 9 ) 0 0 0 2 5 - 0
116
S.S. Shapiro et al./Lithos 48 (1999) 115-133
1. Introduction The weak association between platforms and shields and long-wavelength geoid height anomalies (Shapiro et al., 1999), as well as the near constancy of continental freeboard (e.g., Wise, 1974) suggest that the continental tectosphere did not form simply by conductive cooling. Jordan (1975, 1978) proposed that the thick, cold, continental chemical boundary layer (CBL) inferred from the analysis of seismic data (see also, for example, more recent studies by Grand, 1994; Su et al., 1994; EkstriSm and Dziewonski, 1995; Masters et al., 1996) is stabilized against convective disruption by compositional variations that yield neutral buoyancy (i.e., the continental tectosphere and neighboring oceanic material have the same density profile). These compositional variations have been attributed to a depletion, relative to that from the source of mid-ocean-ridge volcanism, of the denser basaltic constituents (garnet and clinopyroxene) in the continental tectosphere (Jordan, 1978). Monte Carlo simulations indicate that the strong association between platforms and shields and upper-mantle shear-wave anomalies is not simply fortuitous (Shapiro, 1995). This global relationship supports the hypothesis (Jordan, 1975) that these thick CBLs translate coherently with continental plate motions. Combining this conjecture with the measured ages of South African diamond inclusions (e.g., Richardson et al., 1984) and ages obtained from r h e n i u m - o s m i u m and other isotope systematics
(Walker et al., 1989; Pearson et al., 1995) supports the supposition that the continental tectosphere could remain intact in the convecting mantle for times in excess of a billion years (Jordan, 1978). If the tectosphere is to survive in a convecting mantle, it must be stable both to double diffusive instabilities resulting from compositional buoyancy (e.g., Stevenson, 1979) and to tractions from the convecting mantle in which it is immersed. In this study, we investigate primarily the former. Our aim is to quantify the role of viscosity and compositional buoyancy in determining whether a tectosphere would undergo spontaneous disintegration. The boundary conditions in our model are chosen to suppress thermal anomalies associated with the background large-scale mantle convection. We consider the effects of activation energy, compositional buoyancy, and dependence of rheology on stress. We further constrain the range of acceptable parameters by requiting that they not only produce long-term CBL stability, but also create density distributions that yield geoid height anomalies consistent with those observed over platforms and shields (Shapiro et al., 1999).
2. Numerical formulation We use a double-diffusive version of the finiteelement program, ConMan (King et al., 1990), to
600
(km)
(%1
x (km)
Fig. 1. Contours of initial composition (left) and temperature (mirrored -- fight). Dimensionless composition is contoured in increments of 0.1, with C = 1 at the top and C = 0.1 at the base of the CBL. Dimensionless temperature is contoured in increments of 0.1, with T = 0 at the top and T = 1 at the base of the TBL. The C = T = 0.1 contours are thick. Fluctuations in the initial temperature field are due to the superposition on the temperature field of a white noise perturbation with a zero mean and a peak-to-peak amplitude of 0.01. Composition is determined from the unperturbed temperature field according to Eq. (9). The temperature at the base of the CBL, TCBL,is 1170~ {0.9}. The center frame displays, as a function of depth, the difference between the average mid-tectosphere (x < 200 km) density and the average lateral density (see Eq. (10)) for B = 0 (dashed line), B = 1 (thin line), and B = 1.5 (thick line).
117
S.S. Shapiro et al./Lithos 48 (1999) 115-133
solve numerically the advection-diffusion equations for flow of an incompressible, infinite Prandtl number fluid in a two-dimensional Cartesian domain. With two fields affecting density" temperature, T, and composition, C, the relevant (dimensionless) equations are those of momentum balance: =
Vp
-
Ra (;r + 8C)
(1)
continuity: Vu =0
(2)
where E* is the activation energy, Toff is the offset for dimensionless surface temperature required for dimensionless T = 0 to correspond to the = 273 K surface temperature of Earth. The background viscosity, ~7~, implicitly accounts for pressure variations, including the effects of phase changes. A generic form for non-Newtonian viscosity is r/NN = ~Tr~(~.0/r)n- 1, where ~- is the second invariant of the stress tensor, TO is the stress value when the Newtonian and non-Newtonian viscosities are equal, and n, the power law exponent, is assumed to be three for
conservation of energy (with no internal heating): OT
= - u V ; r + v2;r
(3) ]
and its compositional analog"
/
I I
0C 0t
1 = -uVC+
Le
(4)
VZc
where r/ is dynamic viscosity, u velocity, p pressure, t time, Le Lewis number (ratio of thermal to compositional diffusivity), and ~ the unit vector in the direction of increasing depth. The thermal Rayleigh number is Ra T - c ~ g p A T d 3 / K T ~ ) l where ce is the coefficient of thermal expansion, g the acceleration due to gravity, p the density, AT the difference between the temperature at the bottom and that at the top of the domain of depth d, KT the thermal diffusivity, and r/~ a reference value of dynamic viscosity we define to be the viscosity corresponding to dimensionless T = 1. The buoyancy number, B =- A p c / p c e A T , with A Pc the difference in density due to a unit change in composition, describes the ratio of compositional to thermal buoyancy. Unlike thermal gradients, which evolve through the diffusion of heat over geologic time scales, compositional gradients are essentially unaffected by solid-state diffusion; hence Le is effectively infinite. Owing to numerical constraints, however, we are limited to Le < 100 (Brooks, 1981). We define a temperature-dependent Newtonian viscosity, r/N, using an Arrhenius law (e.g., King, 1990): E* r/N ( T ) = ~71 exp T + Toff
-- f-------I "Jr-To7
(5)
i
|
"''I""
~
I
500
,
1020
,
"i;25 viscosity (Pa s)
Fig. 2. Newtonian viscosity profiles based on background viscosities (a) NLO (thick line) and (b) HGPA (thick line), and evaluated using the initial temperature field of the mid-tectosphere and three activation energies: E*f (dash-dotted lines), E*f/3 (dashed lines), and E*f/9 (thin lines), where E*f = 522 kJ mole-1. The dotted lines represent the viscosity profile corresponding to the initial mid-oceanic temperature profile. Note: we do not model NLO's 100-fold increase in viscosity at 670 km depth because its effect on our experiments is insignificant (Shapiro, 1995).
118
s.s. Shapiro et al./Lithos 48 (1999) 115-133
our n o n - N e w t o n i a n ex p e r i m e n t s . Since strain rates are additive, an effective viscosity, ~eff, that in the limit of low stress yields N e w t o n i a n creep and in the limit of high stress yields n o n - N e w t o n i a n creep, can be written as r/eff = [r/~ 1 + r/~ 1 ] - 1 . W e use a value of ~'0 = 1 M P a (10 bars) to define the transition b e t w e e n N e w t o n i a n and n o n - N e w t o n i a n r h e o l o g y and, to avoid n u m e r i c a l p r o b l e m s , we fix the maxim u m d i m e n s i o n l e s s viscosity at ~ c u t / ~ l , w h e r e '0cut = 10 5. B e c a u s e this viscosity cutoff reduces the strength of the u p p e r m o s t mantle, we simulate the effect of this strong layer by i m p o s i n g no-slip b o u n d a r y conditions at the surface.
Table 2 Non-Newtonian rheology: experimental parameters and resulting (i) geoid height anomalies (gN) over the tectosphere, and (ii) depth of the base of the tectosphere CBL (ZcBL)- Both quantities are calculated at 1000 My. We keep all entries in each column to the same place for ease of reading even though not all digits are significant. We do not list the results with E* = 80 kJ molebecause these calculations result in such a rapid destruction of the tectosphere that assigning a thickness is meaningless. See Fig. 8 for a graphical representation of this table E*
B
"Ob (z)
g N (m)
ZCBL (km)
0.0
HGPA NLO HGPA NLO HGPA NLO HGPA NLO HGPA NLO HGPA NLO
- 10 _+5 - 17 _+11 - 12 _+7 - 2 _+5 - 2_ 1 10 _ 6 - 68 +_42 - 83 _ 48 - 11 _+9 - 19 + 11 21 _+10 14 +_8
92 138 304 320 289 271 285 320 329 348 340 348
(kJ mole- 5)
174
1.0 1.5
3. Experimental design and parameters
522
In this study, w e address the stability of a C B L e x p o s e d to c o n v e c t i v e and b u o y a n c y stresses while not explicitly including all of the effects of a convecting mantle. M o d e l i n g n u m e r i c a l l y a d o m a i n the size of Earth with a realistic R a y l e i g h n u m b e r , and t e m p e r a t u r e and s t r e s s - d e p e n d e n t viscosity, is computationally intensive e v e n in t w o - d i m e n s i o n s be-
Table 1 Newtonian rheology: experimental parameters and resulting (i) geoid height anomalies (gN) over the tectosphere, and (ii) depth of the base of the tectosphere CBL (ZcBL). Both quantities are calculated at 1000 My. We keep all entries in each column to the same place for ease of reading even though not all digits are significant. We do not list the results with E* = 80 kJ mole-1 because these calculations result in such a rapid destruction of the tectosphere that assigning a thickness is meaningless. See Fig. 8 for a graphical representation of this table E* (kJ mole- 1)
B
"i"]b (z)
g N (m)
ZCBL (km)
174
0.0
HGPA NLO HGPA NLO HGPA NLO HGPA NLO HGPA NLO HGPA NLO
- 37 _+28 - 62 _+40 5 +_3 - 8 _+5 14 +_8 21 _+10 - 131 +_86 - 119 _+70 - 53 + 34 - 4 2 _+20 - 13 _+8 - 3 _+5
216 250 284 287 297 302 317 309 346 346 346 346
1.0 1.5 522
0.0 1.0 1.5
0.0 1.0 1.5
cause of the high spatial and t e m p o r a l resolution required to m o d e l accurately the flow globally. Our t ect osphere is i m m e r s e d in a hot (and h e n c e r e d u c e d viscosity) i sot hermal and i s o c h e m i c a l e n v i r o n m e n t . W e obtain basal tractions in the fraction of a m e g a pascal range, c o m p a r a b l e to estimates for intraplate sublithospheric tractions on Earth (e.g., H a g e r and O ' C o n n e l l , 1981), so this a p p r o x i m a t i o n s e e m s reasonable. (Stresses in subduction zone e n v i r o n m e n t s are likely s o m e w h a t higher, but, as di scussed b e l o w , regions with p r e s e r v e d t ect osphere typically h a v e b e e n far f r o m subduction zones for m o s t of their history.) W e solve our s y s t e m of equations in a t w o - d i m e n sional Cartesian d o m a i n using a 76 • 38 grid of square e l e m e n t s (see Shapiro (1995) for a discussion of the sensitivity of the results to grid resolution, aspect ratio, and symmet ry). W e begin all of our e x p e r i m e n t s with an " o c e a n i c " t hermal b o u n d a r y layer ( T B L ) of 100 k m {0.13} and a " c o n t i n e n t a l " T B L of 400 k m thickness {0.53} a b o v e a region of u n i f o r m t e m p e r a t u r e (Fig. 1). (To facilitate rescaling our m o d e l results to other plausible initial conditions with thinner or thicker T B L ' s, we present d i m e n s i o n -
S.S. Shapiro et al./Lithos 48 (1999) 115-133
t
0 My; Vmax
34 cm/y,r
119
tOtect-11" Obase--2 (mW/m2)
9
,'
/
l
l
600 t
l
t
l
I
'
150 My; V m a x - 7 cn~,yr
0
/
.Qtect
t = 500 My; V,m a x = 9 cm/,yr
o
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.,.
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.
.
.
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.
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(d)
Y
600
x (kin)
(%)
Fig. 3. Parameters: E*f = E*f/3, B = 0, n = 3, r/b(Z) = NLO. Four frames: t = (a) 0, (b) 150, (c) 500, and (d) 1000 My. Each frame contains (left) contours of composition (purely a tracer field having no effect on the dynamics of the fluid) with superposed velocity arrows, (center) the difference, as a function of depth, between the average mid-tectosphere (x < 200 km) density and the average lateral density (see Eq. (10)), and (mirrored right) contours of temperature with superposed velocity arrows. Contour levels as in Fig. 1.
120
S.S. Shapiro et al./Lithos 48 (1999) 115-133
less parameter values within brackets.) We apply the following boundary conditions along the top (z = 0): ux=0
(6a)
uz=O
(6b)
T = 0~ {0}
(6c)
OC
-0 Oz along the bottom (z = 760 km {1.0}),
(6d)
rzz=O ux=O
(7a) (7b)
0T --
=0
Oz OC
(7c)
-0 Oz along the sides ( x - 0, 1520 km {2.0}),
(7d)
~-xz-O
(8a)
ux=0
(8b)
OT Ox OC
=o
senting an ocean and the other a continental tectosphere. We obtain our initial temperature field by solving the heat conduction equation subjected to the above temperature boundary conditions and a fixed temperature, T = 1300~ {1.0}, along the base ( z 400 km {0.53}) and side (x < 800 km {1.05}) of the tectosphere TBL. We remove these supplementary boundary conditions once the initial temperature field is formed. The compositional field represents the degree of basalt depletion with respect to the oceanic average, with a higher value of C representing a larger amount of depletion and yielding a lower normative density. Following the hypothesis of Jordan (1978, 1988) that, within the continental tectosphere, contours of constant composition are parallel to isotherms, we create an initial (dimensionless) composition field (Fig. 1) that is a function of the initial (dimensionless) temperature field:
C=I-T,
0~
C = 0,
T > TCB L
T~
TCB L
(9)
(8c)
=0 (8d) Ox and beneath the oceanic TBL (x > 800 km {1.05}; z = 100 km {0.13}): The thermal boundary condition at the bottom of the domain and at the base of the oceanic lithosphere were designed to suppress hot plumes and small-scale convection beneath oceanic regions, respectively. Our initial temperature field (Fig. 1) contains two adjoining TBLs of different thicknesses, one repre-
where TcBL = 1170~ {0.9} defines the temperature at the base of the CBL. It is not essential that TcBL have this particular value. Somewhat larger values lead to initial conductive thickening of the TBL while somewhat smaller values lead to the lower part of the TBL dropping off into the fluid below (see Shapiro (1995)). We investigate buoyancy ratios of 0, 1, and 1.5, where B - 0 corresponds to density unaffected by composition, B - 1 to the isopycnic hypothesis of Jordan (1988), and B - 1.5 to a tectosphere with net positive buoyancy.
Fig. 4. Model parameters as in Fig. 3. (a) Geoid height anomalies (gN) at t = 0 (dash-dotted line), 100 (thin solid line), and 1000 (thick solid line) My. (b) Dynamic topography (h) at t-- 0 (dash-dotted line), 100 (thin solid line), and 1000 (thick solid line) My. (c) Viscosity field (7) with superposed velocity arrows (left) and second invariant of the stress tensor (~'(II)) (mirrored fight) at t = 0. Viscosity contours are spaced by factors of 100, with the thick line representing the lowest contour level (102~ Pa s). For the stress field, the thick line represents the lowest contour level (0.5 MPa) and each succeeding contour indicates a stress value a factor of two larger than that for the immediately preceding contour. (d) Viscosity field (7) with superposed velocity arrows (left) and second invariant of the stress tensor (~'(II)) (mirrored fight) at t = 1000 My. Contour intervals as in (c). (e) Initial composition field subtracted from the composition field at t-- 1000 My (left) and initial temperature field subtracted from the temperature field at t-- 1000 My (mirrored fight). Dimensionless contours are spaced in increments of 0.1 with dashed lines representing a loss of composition/temperature and thick solid lines representing a gain. The zero contours are shown with thin solid lines. (f) Area (A) of the - 0 . 1 difference contour, normalized by the area of the initial oceanic and tectosphere CBL, representing a loss of composition (thin line, open circles), and the change (A ZCBL) in the depth of the base of the tectosphere CBL (C-- 0.1) at 1000 My expressed as a percentage of the initial depth (thick line, asterisks). The depth of the base of the tectosphere CBL is estimated from the median depth of the C = 0.1 contour within the tectosphere CBL. (g) Conductive heat flux (Q) through the surface of the tectosphere (thin line, open circles) and advective heat flux through the base of the domain (thick line, asterisks).
(,q~) ~
(,~)
S
. zv :V
(O)a~ z / ~
x
(t) x
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s.s. Shapiroet al./Lithos 48 (1999) 115-133
122
For background viscosity profiles T~b(Z), we use the models H G P A (Hager, 1991) and NLO (Nakada and Lambeck, 1989) (Fig. 2). We base our selection of activation energies on the estimate for dry olivine of E* = E~*ef- 522 kJ mole-1 by Ashby and Verrall (1977); we use E* =E~*f, E*f/3, and E*f/9 to explore the sensitivity of tectosphere stability to activation energy (Tables 1 and 2). Fig. 2 shows, for each activation energy used, the corresponding initial mid-oceanic and mid-tectosphere Newtonian viscosity profiles. In all of our numerical experiments, we use representative values for the following quantities" ce = 3 • 1 0 - 5 ~ l, g = 9.8 m s-2, p = 3.5 x 10 3 kg m -3 and KT = 10 -6 m 2 s -1
4. Buoyancy contrast One can begin to analyze the stability of a particular thermal and compositional structure by calculating the continent-ocean buoyancy contrast, i.e., by calculating at each depth the difference in density between the average mid-tectosphere ( x _< 200 km) value and the laterally averaged value (Fig. 1):
=- ceAT[(T+ BC>lx<_2OOkm--
BC>x]
P (10) For example, a negative value of ~ p ( z ) / p indicates that at depth z, the central region of the tectosphere is lighter, on average, than the average of the ocean and continent values. Considering ~ p / p as a function of depth allows one to predict whether a structure might tend to remain near its initial configuration. As one can see from the plots of ~ p ( z ) / p for B = 0 and B = 1 in Fig. 1, a structure with B = 1 has a greater chance for survival than a structure with B = 0 because, with B = 0, the mid-tectosphere region is much denser than the surrounding material. Of course, this plot neither tells us what structures, if
any, are stable nor how an unstable structure might disintegrate. In the subsequent discussion, we take 1000 My as the characteristic time at which to assess stability. By this time the CBL has either been destroyed or the fluid flow is sufficiently regular that one can reliably make predictions concerning longterm stability.
5. Compositional buoyancy: effect on boundary layer stability To illustrate the effect of composition-induced buoyancy on boundary-layer stability, we discuss in detail the evolution of two cases that differ only in the value of B. Since an acceptable model of the continental tectosphere must satisfy both the longevity and the gravity constraints, at 1000 My we calculate the depth to the base of the CBL, ZCBL, and estimate the associated geoid height anomaly, 8 N (Tables 1 and 2). In the first example, we take E'f~3, B = 0, and n = 3, which leads to very rapid destruction of the tectosphere CBL. With B = 0, composition is simply a tracer field it has no effect on the motion of the fluid. At 1000 My, the CBL is essentially gone, having been washed away by the flow driven by the lateral variations in density (Fig. 3). The tectosphere-ocean buoyancy contrast, ~ p ( z ) / p , decreases in magnitude and, as the tectosphere CBL disappears, becomes non-zero only at shallow depths. The average geoid height anomaly associated with the beginning of the experiment is much greater in amplitude than those observed over platforms and shields (e.g., Shapiro et al. (1999)) (Fig. 4a). Of course, as the source of the density contrast, the tectosphere TBL disappears, the average geoid height anomaly decreases accordingly. Similarly, the variation in dynamic topography is unreasonably large when compared with the near constancy through
Fig. 5. (a) Parameters: E* = E'f/3, B = 0, n = 3, Tlb(Z) = NLO (Fig. 3). Viscosity field ('q) with superposed velocity arrows (left) and second invariant of the stress tensor (~-(II)) (mirrored right)at t = 0. Velocity scaling is clipped at Ucut = 1 cm/year to exhibit lower values more clearly. Contour intervals as in Fig. 4c. (b) Viscosity field (r/) with superposed velocity arrows (left) and second invariant of the stress tensor (-r(II)) (mirrored right) at t= 1000 My. Velocity scaling as in (a). Contour intervals as in Fig. 4c. (c) Parameters: E* = E*f/3, B-- 1.0, n = 3, ~Tb(Z)= NLO (Fig. 6). Viscosity field (r/) with superposed velocity arrows (left) and second invariant of the stress tensor (~'(II)) (mirrored right) at t = 0. Velocity scaling as in (a). Contour intervals as in Fig. 4c. (b) Viscosity field (r/) with superposed velocity arrows (left) and second invariant of the stress tensor (-r(II)) (mirrored - - right) at t = 1000 My. Velocity scaling as in (a). Contour intervals as in Fig. 4c.
123
S.S. Shapiro et al./Lithos 48 (1999) 115-133
the tectosphere much of the flow occurs in the Newtonian regime, although a substantial amount also occurs in regions of high stress (Fig. 5a and b). At 1000 My, the tectosphere is gone, so the size of
time of Earth's continental freeboard (e.g., Wise, 1974) (Fig. 4b). The initial viscosity and stress fields (Fig. 4c) show that the transition between Newtonian and non-Newtonian rheology occurs near the base of
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x (km)
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124
S.S. Shapiro et al./Lithos 48 (1999) 115-133
"Vmax=~m/yr
.
"
150 My; V m a x
4 crn(,yr
.Qtect
3 (m~y/m
11; Qbase
N
600
1
t = 500 My; V m a x = 6 cm(,yr
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t = 1000 My; V m a x = 3 Clg/yr ' ~
4oo
tect ----12"
,
.
.
_
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.
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_ _d
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.
2_
=
E ; e*f / 3
,
0 (%)
1 0
500
~
9
%
%
1000
I
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1500
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B = 1.0, n = 3, r/b(Z) = NLO. Four time frames: t = (a) 0, (b) 150, (c) 500, and (d) 1000 My. Frames as
125
S.S. Shapiro et al./Lithos 48 (1999) 115-133
=
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_ _=
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,
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40
q
(g)
t"q
0
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t(My) Fig. 7. Parameters as in Fig. 6. Frames as described in Fig. 4.
t(My)
126
S.S. Shapiro et al./Lithos 48 (1999) 115-133
the region of high stress is significantly reduced, as is the region of high viscosity (Fig. 4d). Subtracting the initial from the final composition (and temperature) fields illustrates which regions have gained or lost composition (and heated up or cooled down) and by how much (Fig. 4e). By plotting the area, A, of the - 0 . 1 composition difference contour (normalized to the combined area of the initial oceanic and continental CBLs) as a function of time (Fig. 4f), we see that most of the composition is removed from the tectosphere CBL within the first 50 My. After this time, the rate of removal diminishes dramatically, decreasing slowly to zero at about 600 My. After the initially weak (i.e., easily deformed) material is quickly washed away, the remnant continental CBL weakens gradually as a result of the combination of the hot material flowing along its base and the strong temperature-dependence of the material's viscosity. We interpret this temporal pattern as indicating the presence of two instabilities, a mechanical mode (t < 50 My) and a thermal ablation mode (t > 50 My). The change in the depth to the base of the CBL, A ZCBL-- ZCBL(0) --ZCBL(t), expressed as a percentage of the initial CBL thickness (ZcBL(0)), varies with time in a manner similar to A(t) (Fig. 4f). Such a correspondence is reassuring since both of these quantities were devised independently to estimate, as a function of time, the condition of the CBL. The conductive heat flux through the continental surface (Fig. 4g) increases by only a factor of about t w o (10 m W m -z ) throughout the calculation. The advective heat flux through the base of the domain is more variable. The intervals of large fluxes coincide with part of the tectosphere's TBL falling off and sinking through the base of the domain. Such occurrences are episodic. (Note that the time interval at which we stored the fields needed to compute regional fluxes is too coarse to fully resolve the peaks in the flux-time curve.) When we repeat the above experiment with B = 1, the results differ significantly. The CBL remains largely intact after 1000 My, although its initially horizontal base becomes rounded (Fig. 6). The function ~p(z)/p changes shape, gradually forming a profile which indicates that a cold, dense upper section of the tectosphere is being partially supported from below by a light CBL opposite to our initial
condition where the TBL extends beneath the CBL, causing the small positive deviation from zero in ~p(z)/p. This dense upper region is caused by the conductive cooling of the upper section of the tectosphere with composition effectively unable to diffuse, the isopycnic condition is no longer satisfied in this region. Throughout the experiment, both the average geoid height anomaly and the dynamic topography associated with the tectosphere CBL have geophysically reasonable values (Fig. 7a and b). Due to the addition of compositional buoyancy, the second invariant of the stress is reduced relative to the above experiment (B = 0). This lower stress yields a correspondingly higher viscosity field (Fig. 5c, Fig. 6b, Fig. 7c and Fig. 7d) which leads to a more stable CBL. The changes in the composition and temperature fields after 1000 My are confined to a much smaller area than in the previous experiment (Compare Fig. 4e and Fig. 7e). Again, the initially weak material is removed quickly from the tectosphere, although with the stabilizing effect of compositional buoyancy more material remains (Fig. 7f). Further, the higher viscosity due to the lower stress than in the B = 0 case inhibits the thermal ablation process so that it is barely observable in A(t). Here, A(t) and A ZcBL(t) diverge at about 200 My. After this time, A(t) is essentially constant whereas A ZCBL(t) decreases slightly, indicating that the CBL is thickening. From Fig. 6c and d, one can see that this thickening occurs in the center of the tectosphere CBL as a consequence of the cold "blobs" detaching from the tectosphere TBL. The plot of heat flux through the base of the domain (Fig. 7g) shows some of these instabilities. The heat flux through the top of the tectosphere, however, does not vary noticeably with time, holding at a value of about 20 mW m -2.
6. Bounds on E*, B,
and "qb(Z) from longevity
and geoid constraints To evaluate the relative effects of (1) activation energy, (2) compositional buoyancy, and (3) rheology on tectosphere stability and the resulting geoid signal, we plot the depth to the base of the CBL and the average geoid height anomaly over the continental tectosphere, at t = 1000 My, for each experiment
S.S. Shapiro et al./Lithos 48 (1999) 115-133
listed in Tables 1 and 2 (Fig. 8). We do not plot results for our experiments with E*/9, which are so
127
unstable that the tectosphere is removed in t << 1000 My, and the calculations terminated.
250
ill
i I
I
I D
I
6 N(m) Fig. 8. The depth to the base of the CBL (ZCBL) (ordinate) and the mean geoid height anomaly (gN) over the tectosphere CBL (abscissa) both at 1000 My. The depth to the base of the CBL is estimated from the median depth to the C = 0.1 contour within the tectosphere CBL. Triangles and squares indicate experiments with activation energies of E* = E* r and E*f/3, respectively. White, gray, and black symbols indicate experiments with buoyancy ratios of B = 0, 1, and 1.5, respectively. Small and large symbols indicate experiments with background viscosity profiles based on HGPA and NLO, respectively. The ordinates of the horizontal dashed lines indicate a (somewhat arbitrary) upper bound of ZCBL based on the inferred thickness of the continental tectosphere (Shapiro, 1995). The abscissas associated with the vertical dashed lines correspond to gNps _+ 2o- as determined by Shapiro et al. (1999). (a) Newtonian rheology. (b) Non-Newtonian rheology. Circles represent experiments with a background viscosity profile determined by NLO and an activation energy of E* -- E'f~ 1.25. White and gray symbols indicate experiments with buoyancy ratios of B = 0 and 1, respectively.
128
S.S. Shapiro et al./Lithos 48 (1999) 115-133
In both the Newtonian and non-Newtonian experiments, using an activation energy of 522 kJ mole -1, corresponding to dry olivine (Ashby and Verrall, 1977), assures stability regardless of the amount (within reasonable limits) of compositional buoyancy present. However, not all of these experiments produce geoid height anomalies consistent with those observed for platforms and shields (Shapiro et al., 1999). In fact, by comparing the average geoid height anomalies resulting from the E* = E~*f experiments (triangles in Fig. 8), one can see that simply satisfying the isopycnic hypothesis is insufficient to ensure a geoid height anomaly consistent with the observed geoid associated with platforms and shields one must also consider the dynamics of the flow. For example, the Newtonian experiments with initial B = 1.5, but not with B = 1, satisfy the geoid constraint. From the corresponding, more realistic, experiments with stress-dependent rheology, we estimate that the initial B is likely between about 0.9 and 1.3, depending on the background viscosity profile (Fig. 8b). (We refer to the "initial" B because, after 1000 My, both the temperature and composition are modified and the local value of B changes. For example, for the experiment shown in Fig. 6, at 1000 My, for z < 400 kin, 8p > 0 implies B < 1, while for z > 400 km, 8 p < 0 implies B > 1.) With an activation energy one third the above value (E~ef/3) and a stress-dependent rheology, compositional buoyancy plays a major role in stabilizing the continental tectosphere (compare the open with the shaded squares in Fig. 8b; compare also Figs. 3 and 6). After 1000 My, the CBLs with B = 1 are roughly 200 km thicker than those containing no compositional buoyancy. Compositional buoyancy has a similar effect on stability for the corresponding Newtonian experiments, except for those characterized with an activation energy of E ~*e f / 3 . In this case, B = 1 results in CBLs that are only about 50 km thicker than the corresponding CBLs that contain no compositional buoyancy. By comparing the Newtonian to the non-Newtonian experiments, we see that compositional buoyancy plays a larger stabilizing role with a non-Newtonian rheology. Compositional buoyancy reduces the stress within the boundary layer, which in conjunction with the stress dependence of viscosity, causes an increase in viscosity which stabilizes the CBL.
The two background viscosity models yield continental tectosphere thicknesses that are always within about 50 km of each other. In most, but not all cases, the model with a background viscosity described by NLO is the more stable one.
7. Discussion
The most important question our numerical experiments were designed to address is whether under any circumstances a thick, cold root beneath continents can be stable over time scales of a billion years or more. The alternative is that these roots are parts of massive convective downwellings (e.g., Pari and Peltier, 1996). We find that the effects of temperature dependent viscosity can stabilize these roots, with only slow ablation by small-scale convection. The wisps of cold material sinking into the deeper interior in our models are consistent with the seismic observations of Li et al. (1998), who found that beneath the deep root below the eastern United States there is little perturbation in the depth of the 400 km seismic discontinuity. They conclude that any cold downwellings in the transition zone in the region they studied must be weak ( < 50 K) and/or small-scale. Conclusions drawn from studies of boundary-layer dynamics depend strongly on assumptions concerning the temperature and stress dependence of viscosity and the magnitude of %, the typical value of background stress in the convecting mantle. From an analytical analysis of the stability of a constant viscosity continental tectosphere described by linear gradients in composition and temperature, assuming 77 = 10 21 Pa s, Stevenson (1979) found modes of instability with characteristic growth times as short as about 200 My w an order of magnitude less than that required by the above age constraints. If one considers the temperature dependence of viscosity and the fact that continents are cold, a constant viscosity of r/= 1021 Pa s is an unrealistically low estimate (e.g., Simons and Hager, 1997). An increase of only one order of magnitude would yield characteristic time constants comparable to the age of Earth. In addition, the strong temperature dependence of viscosity helps to confine the flow to a very
129
S.S. Shapiro et al./Lithos 48 (1999) 115-133
limited region, further stabilizing the tectosphere, as discussed below. In the high-stress regime, where zc >> 1 MPa (10 bars), Kincaid (1990) concluded that viscosity, not compositional buoyancy, is responsible for achieving long-term stability. Shapiro (1995) further demonstrated that, with zc 6 MPa (60 bars), 10-20 times that considered to be appropriate for most of Earth (e.g., Hager and O'Connell, 1981), a viscosity increase of a factor of about 20 between the TBL and the surrounding mantle is sufficient to maintain stability, regardless of the amount of compositional buoyancy (within reasonable bounds). These studies probably overestimate the role of tractions from mantle convection because, due to numerical constraints, they were carried out at a Rayleigh number lower than appropriate for Earth. Convective stresses scale as "ro=pgdaATRa~/3; since the value of AT assumed in these studies is a realistic one, higher Rayleigh numbers, corresponding to lower viscosities, result in thinner boundary layers, and lower stresses. Our transition stress value is based on a small grain size about one mm (Ashby and Verrall, 1977). As grain size increases, the transition stress
0 t = 1000 My; Vclip = 1 cm/yr
200-
decreases, so our choice of % = 1 MPa (10 bars) is a conservative one in the following sense: If we had assumed a larger grain size, the fluid within and beneath the tectosphere would have been more viscous, and the tectosphere would have been more likely to survive. In the low-stress regime, we find that destruction is achieved in two ways: (1) through a mechanical removal of material and (2) via a thermal ablation process in conjunction with the mechanical process. The initially weak regions of the tectosphere are washed away quickly by convective processes; the remaining material is removed more slowly. As the base warms through conduction, it becomes weaker due to viscosity's inverse dependence on temperature. Then, in its weakened state, it is swept away by the convection currents. To estimate the viscosity required to prevent this mechanical removal, we consider the viscosity corresponding with this "ablation front". For the experiments which yield CBLs that are stable over a billion year time scale (Fig. 8), the viscosity corresponding to the edge of the ablation front, where velocities become negligible, is approximately 10 20.5 Pa s (for a representative example, see Fig. 9). Once the viscosity of the tectosphere
--%_---i
\
r
i
\
~ ~ ~\..
- - ~
=
400
1500
1000
500
0
Fig. 9. Model parameters as in Figs. 6 and 7. Viscosity field (r/) (solid lines) with velocity arrows and the change in the composition field (see Fig. 7) (dashed lines) superposed; t = 1000 My. Velocity scaling is clipped at /"cut= 1 c m / y e a r to exhibit lower values more clearly. Contour intervals as in Fig. 4.
130
S.S. Shapiro et al./Lithos 48 (1999) 115-133
material is about a factor of ten greater than that of the underlying mantle, negligible flow occurs similar to the result from high-stress models (Shapiro, 1995). Further support for this interpretation comes from the work of Conrad and Molnar (1997). They used a semi-analytic approach to investigate RayleighTaylor-type instabilities of a more dense fluid layer of thickness, h, overlying a uniform halfspace. Within the layer, density increases linearly with distance above the boundary, as A p z/h, and viscosity varies exponentially, as r/0 exp(z/L). Their results show that flow is essentially confined to a layer of thickness z = 2L, corresponding to a depth range over which the viscosity varies by a factor of 10. As is the case with our numerical experiments, there is negligible flow excited in regions with higher viscosity. For a ratio L / h ~ 0.03, typical Rayleigh-Taylor growth times are of order 30 ~qo/ApgL. Assuming representative values of density contrast, A p = 100 kg/m3; tectospheric thickness, h = 300 km; reference viscosity, r/0 = 1 0 2~ Pa s; and viscosity e-folding distance, L = 10 km; the characteristic growth time is ~ 50 My. Such a short growth time is consistent with the results of our numerical experiments, which show a subtectospheric drip developing on a comparable time scale. Once this sublithospheric drip strips away the initial layer of thickness 2 L ~ 20 km, the gradient in viscosity at the base of the tectosphere is much sharper, resulting in a situation where L is of order 1 km. Since the growth time is inversely proportional to L, the rate at which the tectosphere ablates decreases by a comparable factor, with a characteristic growth time ~ 1 Gy. Fleitout and Yuen (1984) demonstrated that the combination of pressure- and temperature-dependent viscosity can help to stabilize a thick thermal boundary layer from convective disturbance. The temperature-dependence of viscosity stabilizes the cold (shallow) part of the TBL while the pressure-dependence of viscosity stabilizes the warmer (deeper) part. Our numerical representation of the continental tectosphere is stable even without the stabilizing effects of pressure-dependent viscosity. Doin et al. (1997) have extended these calculations, investigating the effects of rheology dependent on temperature, pressure, and composition, in a do-
main of width 2680 km and depth 670 km. They enforce a tectonic regionalization using velocity boundary conditions, with one third to one half of the surface, representing a continent, pinned to the surface, and the remaining domain driven by imposed horizontal velocities, representing oceanic plates. The velocity boundary conditions change with time such that the subduction zone is periodically adjacent to either edge of the tectosphere region, with one side or the other of the craton experiencing subduction every 90 My. They find that viscosity is the most important parameter in determining whether the tectosphere is stable, and that compositional buoyancy is not a primary contributor for the value of E* that they use, 310 kJ mole-1 (corresponding to 0.6 E'f). For models with strong pressure dependence of viscosity, there are two preferred lithospheric thicknesses, one corresponding to mature oceanic lithosphere and the other to the thickness of the subcontinental tectosphere. Doin et al. (1997) find somewhat higher rates of tectosphere ablation than do we. One reason is that the activation energy that they used, 310 kJ mole-l, is less than the value that we used, 522 kJ mole-l, the estimate for dry olivine (Ashby and Verrall, 1977). Also, their models have flow confined to the upper mantle, so there is strong shear between the base of their continental TBL and the bottom of their computational domain. Perhaps most importantly, their "continents" are narrow (900-1350 km wide) and are bounded by subduction zones at intervals of < 100 My. In contrast, on Earth, tectosphere is only rarely adjacent to a subduction zone. For example, Bostock (1998, Bostock, 1999) interprets the seismic structure of the Slave craton as resulting from a fossil subduction zone that has been preserved for > 1.9 Gy since the suturing of the Fort Simpson terrain and the Slave province. Forte et al. (1995) suggested that the buoyancy profile beneath continents reverses in sign at about 250 km depth. Specifically, Forte et al. (1995) proposed that the negative buoyancy in the upper 250 km of the subcontinental mantle is partially supported by underlying lighter material. Interestingly, some of our acceptable models exhibit this same buoyancy reversal (see, for example, Fig. 6). As we discussed above, this buoyancy reversal is caused by the conductive cooling of the tectosphere. This cool-
s.s. Shapiro et al.,/Lithos 48 (1999) 115-133
ing is dependent on the convecting system in which it is placed. In fact, the existence of a buoyancy reversal is very sensitive to several of our assumptions, with some acceptable models showing this reversal, and others not [see, for example, Fig. B.21 of Shapiro (1995)]. Hence, our study cannot be used to predict accurately whether such a reversal actually exists. For models with viscosity sufficiently high that the tectosphere survives, there is negligible deformation of the tectosphere. Thus, heat transport through the tectosphere in our models is controlled by conduction. The predicted mantle heat flow decreases from the suboceanic region to the interior of the tectosphere, as the depth to a given isotherm increases. Such variation is consistent with the careful analysis of heat flow observations by Jaupart and Mareschal (1999), who estimated variations in mantle heat flow and lithospheric thickness after stripping off the effects of near-surface heat production. They estimate that the conductive part of the subcratonic thermal boundary layer is 200-330 km thick. Only beneath that depth does advective heat transport become important. In contrast, Lenardic (1997) used the results of convection models that, like ours, include the effects of compositional buoyancy, to challenge this interpretation. In Lenardic's models, the viscosity of the material comprising the subcratonic regions is sufficiently low that recirculation within the crust and underlying buoyant material is driven by the convecting mantle. This recirculation leads to a substantial advective contribution to the heat flux. In his models, there is little variation in mantle heat flux between "cratonic" and surrounding regions. In our view, if the tectosphere is to survive, its viscosity must be so high that deformation is negligible; heat transport results from simple conduction, with negligible advective contribution. The results of Jaupart and Mareschal (1999), who explain observed heat flow variations of both short and long wavelengths in terms of observed crustal heat production and a conductive model of heat transport through the tectosphere, support our interpretation. In summary, the joint application of longevity and gravity constraints allows us to evaluate the importance of specific properties of a continental tectosphere in the low-stress regime. High viscosity is
131
crucial for the long-term survival of the tectosphere. Flow models characterized by the activation energy for dry olivine, 522 kJ mole-1, yield stable boundary layers that, once established, are stable, even with no compositional buoyancy present. However, activation energies, say tenfold smaller, are too low; they lead to a rapid (of order 10 My) destruction of the tectosphere. With an activation energy about 20% less than that estimated for olivine, temperature-dependent viscosity alone is sufficient to assure stability (Fig. 8). With lower values of activation energy, stability of an existing tectosphere can be achieved with the inclusion of compositional buoyancy. Compositional buoyancy plays a dual role within a thermal (and chemical) boundary layer: It (1) reduces the stress within the boundary layer and (2) counteracts the thermally-induced density increase. With a stress-dependent rheology, this reduction in stress results in an increase in viscosity which, in turn, inhibits a greater region of the boundary layer from deforming. Removal of volatiles by depletion would also increase the viscosity, providing a plausible mechanism contributing to the stabilization of the tectosphere (Pollack, 1986). If, for realistic activation energies, compositional buoyancy is not required to maintain a stable tectosphere, it is interesting to ask why the geoid observations (Shapiro et al., 1999) indicate that B ~- 1? If the tectosphere formed by advective thickening, the results of our numerical experiments provide a plausible answer. Formation via advective thickening requires that the material that now constitutes the rigid tectosphere was ductile enough to deform and thicken at the time of formation of the proto-tectosphere. Thus, the proto-tectosphere was likely to have been somewhat warmer than mature tectosphere is now in order that it had a sufficiently low viscosity to deform. Since it is the ratio of E * / T that governs viscosity, a higher T is equivalent to a lower E*. As our numerical experiments demonstrate, compositional buoyancy is required to stabilize the tectosphere at lower E*. Thus it seems likely that compositional buoyancy would also be important in stabilizing a somewhat hotter proto-tectosphere, formed under advective thickening, that later completely stabilized by moderate cooling. Such moderate cooling would be consistent with the estimate from the geoid signal associates with cratons
s.s. Shapiro et al./Lithos 48 (1999) 115-133
132 that the p r e s e n t - d a y
B is slightly less t h a n u n i t y
( S h a p i r o et al., 1999).
Acknowledgements W e t h a n k S c o t t D. K i n g for h e l p i n g us to i n c o r p o rate
chemical
variations
into the code,
ConMan,
P e t e r P u s t e r a n d M a r k S i m o n s for their c o n t r i b u t i o n s to o u r v e r s i o n o f ConMan, a n d C l i n t o n C o n r a d for discussions. Adrian Lenardic and Richard O ' C o n n e l l provided
insightful reviews.
This
work
was
sup-
p o r t e d b y N a t i o n a l S c i e n c e F o u n d a t i o n grants E A R 9506427 and C D A - 9 6 0 1 6 0 3 .
References Ashby, M.F., Verrall, R.A., 1977. Micromechanisms of flow and fracture, and their relevance to the rheology of the upper mantle. Philos. Trans. R. Soc. London A 288, 59-95. Bostock, M., 1998. Mantle stratigraphy and evolution of the Slave province. J. Geophys. Res. 103, 21183-21200. Bostock, M.G., 1999. Seismic imaging of lithospheric discontinuities and continental evolution. Lithos., this issue. Brooks, A.N., 1981. A Petrov-Galerkin finite element formulation for convection dominated flows. Ph.D. thesis, California Institute of Technology. Conrad, C.P., Molnar, P., 1997. The growth of Rayleigh-Taylortype instabilities in the lithosphere for various rheological and density structures. Geophys. J. Int. 129, 95-112. Doin, M.-P., Fleitout, L., Christensen, U., 1997. Mantle convection and stability of depleted and undepleted continental lithosphere. J. Geophys. Res. 102, 2771-2787. EkstriSm, G., Dziewonski, A.M., 1995. Improved models of upper mantle S velocity structure. EOS Trans. AGU 76, 421, (abs). Fleitout, L., Yuen, D.A., 1984. Steady state, secondary convection beneath lithospheric plates with temperature- and pressure-dependent viscosity. J. Geophys. Res. 89, 9227-9244. Forte, A.M., Dziewonski, A.M., O'Connell, R.J., 1995. Continent-ocean chemical heterogeneity in the mantle based on seismic tomography. Science 268, 386-388. Grand, S.P., 1994. Mantle shear structure beneath the Americas and surrounding oceans. J. Geophys. Res. 99, 11591-11621. Hager, B.H., 1991. Mantle viscosity: a comparison of models from postglacial rebound and from the geoid, plate driving forces, and advected heat flux. In: Sabadini, R., Lambeck, K., Boschi, E. (Eds.), Glacial Isostasy, Sea-Level and Mantle Rheology. Kluwer Academic Publishers, Dordrecht, 493-513. Hager, B.H., O'Connell, R.J., 1981. A simple global model of
plate dynamics and mantle convection. J. Geophys. Res. 86, 4843-4867. Jaupart, C., Mareschal, J.C., 1999. The thermal structure and thickness of continental roots. Lithos., this issue. Jordan, T.H., 1975. The continental tectosphere. Rev. Geophys. Space Phys. 13, 1-12. Jordan, T.H., 1978. Composition and development of the continental tectosphere. Nature 274, 544-548. Kincaid, C., 1990. The dynamical interaction between tectosphere and large scale mantle convection. EOS Trans. AGU 71, 1626, (abs). King, S.D., 1990. The interaction of subducting slabs and the 670 kilometer discontinuity. Ph.D. thesis, California Institute of Technology. King, S.D., Raefsky, A., Hager, B.H., 1990. ConMan: vectorizing a finite element code for incompressible two-dimensional convection in the earth's mantle. Phys. Earth Planet. Inter. 59, 195-207. Lenardic, A., 1997. On the heat flow variation from Archaen cratons to Proterozoic mobile belts. J. Geophys. Res. 102, 709-721. Li, A., Fischer, K.M., Wysession, M.E., Clarke, T.J., 1998. Mantle discontinuities and temperature under the North American continental keel. Nature 395, 160-163. Masters, T.G., Johnson, S., Laske, G., Bolton, H., 1996. A shear velocity model of the mantle. Philos. Trans. R. Soc. London, A 354, 1385-1414. Nakada, M., Lambeck, K., 1989. Late Pleistocene and Holocene sea-level change in the Australian region and mantle rheology. Geophys. J. Int. 96, 497-517. Pail, G., Peltier, W.R., 1996. The free-air gravity constraint on subcontinental mantle dynamics. J. Geophys. Res., 101, 28, 105-28, 132. Pearson, D.G., Shirey, S.B., Carlson, R.W., Boyd, F.R., Pokhilenko, N.P., Shimizu, N., 1995. Re-Os, Sm-Nd, and Rb-Sr isotope evidence for thick Archaean lithospheric mantle beneath the Siberian craton modified by multistage metasomatism. Geochim. Cosmochim. Acta 59, 959-977. Pollack, H.N., 1986. Cratonization and thermal evolution of the mantle. Earth Planet. Sci. Lett. 80, 175-182. Richardson, S.H., Gurney, J.J., Erlank, A.J., Harris, J.W., 1984. Origins of diamonds in old enriched mantle. Nature 310, 198-202. Shapiro, S.S., 1995. Structure and dynamics of the continental tectosphere. Ph.D. thesis, Massachusetts Institute of Technology. Shapiro, S.S., Hager, B.H., Jordan, T.H., 1999. The continental tectosphere and Earth's long-wavelength gravity field. Lithos., this issue. Simons, M., Hager, B.H., 1997. Localization of the gravity field and the signature of glacial rebound. Nature 390, 500-504. Stevenson, D.J., 1979. Double diffusive instabilities in the mantle. I.U.G.G. 17th Gen. Assembly, I.A.S.P.E.I. Canberra, Australian National University, 72 (abstr.). Su, W.-J., Woodward, R.L., Dziewonski, A.M., 1994. Degree 12 model of shear velocity heterogeneity in the mantle. J. Geophys. Res. 99, 6945-6980.
S.S. Shapiro et al./Lithos 48 (1999) 115-133
Walker, R.J., Carlson, R.W., Shirey, S.B., Boyd, F.R., 1989. Os, Sr, Nd, and Pb isotope systematics of southern African peridotite xenoliths: Implications for the chemical evolution of subcontinental mantle. Geochim. Cosmochim. Acta 53, 15831595.
133
Wise, D.U., 1974. Continental margins, freeboard and the volumes of continents and oceans through geological time. In: Burk, C.A., Drake, C.L. (Eds.), The Geology of Continental Margins. Springer-Verlag Publishers, New York, 45-58.
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Lithos 48 (1999) 135-152
The continental tectosphere and Earth's long-wavelength gravity field Steven S. Shapiro 1, Bradford H. Hager * , Thomas H. Jordan Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
Received 19 October 1998" received in revised form 8 February 1999; accepted 15 February 1999
Abstract To estimate the average density contrast associated with the continental tectosphere, we separately project the degree 2-36 non-hydrostatic geoid and free-air gravity anomalies onto several tectonic regionalizations. Because both the regionalizations and the geoid have distinctly red spectra, we do not use conventional statistical analysis, which is based on the assumption of white spectra. Rather, we utilize a Monte Carlo approach that incorporates the spectral properties of these fields. These simulations reveal that the undulations of Earth's geoid correlate with surface tectonics no better than they would were it randomly oriented with respect to the surface. However, our simulations indicate that free-air gravity anomalies correlate with surface tectonics better than almost 98% of our trials in which the free-air gravity anomalies were randomly oriented with respect to Earth's surface. The average geoid anomaly and free-air gravity anomaly over platforms and shields are significant at slightly better than the one-standard-deviation level: - 1 1 _+ 8 m and - 4 _+ 3 regal, respectively. After removing from the geoid estimated contributions associated with (1) a simple model of the continental crust and oceanic lithosphere, (2) the lower mantle, (3) subducted slabs, and (4) remnant glacial isostatic disequilibrium, we estimate a platform and shield signal of - 8 + 4 m. We conclude that there is little contribution of platforms and shields to the gravity field, consistent with their keels having small density contrasts. Using this estimate of the platform and shield signal, and previous estimates of upper-mantle shear-wave travel-time perturbations, we find that the average value of i?ln p/Oln vs within the 140-440 km depth range is 0.04 _ 0.02. A continental tectosphere with an isopycnic (equal-density) structure @ln p/Olnv s = 0) enforced by compositional variations is consistent with this result at the 2.0o" level. Without compositional buoyancy, the continental tectosphere would have an average 01n p / i ) l n v S ~ 0.25, exceeding our estimate by 10o-. 9 1999 Published by Elsevier Science B.V. All rights reserved. Keywords." Continental tectosphere" Earth; Long-wavelength gravity field; Geoid anomaly; Gravity anomaly
1. Introduction Motivated by seismological evidence (e.g., Sipkin and Jordan, 1975) and the lack of a strong correla-
* Corresponding author. ~Present address" Department of Physics, Guilford College, Greensboro, NC 27410, USA
tion between continents and the long-wavelength geoid (e.g., Kaula, 1967), Jordan (1975) proposed that continents are (1) characterized by thick ( ~ 400 km) thermal boundary layers (TBLs) which translate coherently during lateral plate motions, (2) stabilized against small-scale convective disruption by gradients in density due to compositional variations, and (3) not observable in the long-wavelength gravity
0024-4937/99/$ - see front matter 9 1999 Published by Elsevier Science B.V. All rights reserved. PII: S0024-4937(99)00027-4
136
S.S. Shapiro et a l . / Lithos 48 (1999) 135-152
field. The simple plate cooling model, which enjoys much success in describing the structure of oceanic TBLs, cannot be extended to explain thicker continental TBLs (Jordan, 1978). Instead, Jordan (1978) postulated that the thick continental TBL, continental tectosphere, was formed early in Earth's history by advective thickening and has been stabilized against convective cfisruption by the compositional buoyancy provided by a depletion of basaltic constituents. The isopycnic (equal-density) hypothesis (Jordan, 1988) predicts that the compositional and thermal effects on density cancel at every depth between the base of the mechanical boundary layer and the base of the TBL. Such a structure would be neutrally buoyant with respect to neighboring oceanic mantle, and would not be visible in the long-wavelength gravity field. There has been much discussion during the past 2 decades about the relations among the Earth's longwavelength gravity field, surface tectonics, and mantle convection. For example, there is an obvious association of long-wavelength geoid highs with subduction zones (Kaula, 1972; Chase, 1979; Crough and Jurdy, 1980; Hager, 1984) and with the distribution of hotspots (Chase, 1979; Crough and Jurdy, 1980; Richards and Hager, 1988). Most of the power in the longest wavelength geoid can be explained in terms of lower-mantle structure imaged by seismic tomography (e.g., Hager et al., 1985; Hager and Clayton, 1989; Forte et al., 1993a). This lower mantle seismic structure has been linked to tectonic processes, in particular, to the history of subduction (e.g., Richards and Engebretson, 1992). Although there is general agreement among geodynamicists that most of the geoid can be explained in terms of features such as subducted slabs and lower mantle structure, there is significant quantitative disagreement among the predictions of various models (e.g., Panasyuk, 1998). Thus, it is not possible to estimate with high confidence the "residual geoid" not explained by lower mantle structure. The contribution to the geoid of upper-mantle structures, including variations in the thickness of the crust and lithosphere, is a question whose answer is still disputed. Assuming that plates approach an asymptotic thickness of approximately 120 km after cooling about 80 My, the geoid would be expected to be higher by roughly l0 m over continents and over
midoceanic ridges than over old ocean basins due to the density dipole associated with isostatic compensation (Haxby and Turcotte, 1978; Parsons and Richter, 1980; Hager, 1983). At intermediate to short wavelengths, the expected changes in the geoid over these features are observed (e.g., Haxby and Turcotte, 1978; Doin et al., 1996), but the isolation of the geoid signatures of these features at long wavelengths is problematic. Using broad spatial averages over selected areas, Turcotte and McAdoo (1979) concluded that there is no systematic difference in the geoid signal between oceanic and continental regions. But, Souriau and Souriau (1983) demonstrated that there is a significant correlation between the geoid (spherical harmonic degrees l = 3-12) and the tectonic regionalization of Okal (1977). From degree-by-degree correlations (l = 2-20), Richards and Hager (1988) observed a weak association between geoid lows and shields. On the other hand, Forte et al. (1995) reported that the degree 2-8 geoid correlates significantly (99% confidence) with an ocean-continent function. Were there a significant ocean-continent signal, the continental tectosphere might have a substantial density anomaly associated with it, and might therefore be expected to play an active role in the largescale structure of mantle convection. For example, Forte et al. (1993b) and Pari and Peltier (1996), in their preferred models, assumed linear relationships between seismic velocity anomalies and density anomalies. They proposed dynamic models of the long-wavelength geoid in which the high velocity roots beneath continents are cold, dense downwellings in the convecting mantle. Such downwellings would depress the surface of continents dynamically by about 2 km (Forte et al., 1993b). The lack of significant temporal variation in continental freeboard over geologic time would require that these convecting downwellings be extremely long-lived and translate coherently with the continents (e.g., Gurnis, 1993). On the other hand, Hager and Richards (1989) and Forte et al. (1993b) found the best fits of their dynamic models to the geoid by assuming an unusually small global proportionality between seismic velocity anomalies and density anomalies in the upper mantle. Forte et al. (1995) showed that they could improve their fit to the geoid if they allowed subcontinental regions to have a different proportion-
137
S.S. Shapiro et al./Lithos 48 (1999) 135-152
Table 1 GTR1 (Jordan, 1981) Region Definition Oceans A B C Continents Q P S
1996), referred to the hydrostatic figure of Earth (Nakiboglu, 1982) (Fig. 2a). Although we use GTR1 (and coarser regionalizations created by combining some of these regions) for the bulk of this study, we also compare our results with those obtained using the tectonic regionalizations of Mauk (1977) and Okal (1977), as well as the ocean-continent function. Because the geoid spectrum is red, with the rootmean-square (rms) value of a coefficient of degree 1 decreasing roughly as 1-2 , and because the longest wavelengths are likely dominated by the effects of density contrasts in the lower mantle (Hager et al., 1985), we also investigate the relationship between GTR1 and free-air gravity anomalies. The gravity field at spherical harmonic degree 1 is proportional to 1-1, so the gravity anomalies are expected to have correspondingly smaller long-wavelength variations than the geoid does. We calculate regional averages of the geoid and the gravity field and estimate their uncertainties. Further, we try to refine the estimate of the contribution of the continental tectosphere to the geoid by
Fractional area (%)
Young oceans (0-25 My) Intermediate-age oceans (25-100 My) Old oceans ( > 100 My) Phanerozoic orogenic zones Phanerozoic platforms Precambrian shields and platforms
61 13 35 13 39 22 10 7
ality constant between velocity and density anomalies beneath continents than beneath oceans. To quantify the association of surface tectonics and Earth's gravity field, we investigate the significance of the association between the six-region global tectonic regionalization GTR1 (Jordan, 1981) (Table 1, Fig. 1) and the geoid, EGM96 (Lemoine et al., i
I
A
B
C
Q
P
I
S
Fig. 1. Tectonic regionalization, GTR1 displayedusing a Hammerequal-area projection. See Table 1 for a description of each region.
S.S. Shapiro et al./Lithos 48 (1999) 135-152
138
I
o!
il
~
-lO0 -80
' ........
~-'"';':.,.~:;~,
-60
' . . . . . . ' .......
-40
" ..................
-20
0
Meters
~r;;~,
20
~'~
:'-
40
. . . . . . . . . . . . . . . .
60
80
lO0
139
s.s. Shapiro et al./Lithos 48 (1999) 135-152
subtracting other contributions from the geoid estimates. By combining the upper-mantle shear-wave travel-time anomalies associated with platforms and shields (Shapiro, 1995) and the results from this study, we estimate, with uncertainties, the average of aln p/01n vs within the depth range 140-440 km, and compare our estimate with the isopycnic hypothesis of Jordan (1988).
Table 2 Okal (1977) Region
Definition
Fractional area (%)
D C B A T M S
Ocean (0-30 My) Ocean (30-80 My) Ocean (80-135 My) Ocean ( > 135 My) Trenches and marginal seas Phanerozoic mountains Shields
12.0 30.1 12.3 2.5 10.9 11.6 20.4
2. Tectonic regionalization and inversion GTR1 and regionalizations published by Okal (1977) (Table 2) and Mauk (1977) (Table 3) contain six, seven, and 20 regions, respectively. Both GTR1 and the regionalization of Mauk (1977) are defined on a grid of 5 ~ • 5 ~ cells, whereas the model of Okal (1977) is defined using 15 ~ 2 1 5 ~ and 10~ 2 1 5 ~ cells. The regionalization of Mauk (1977) allows for as many as 10 regions to be represented in a given cell, while the other regionalizations are defined with only one region per cell. In GTR1, the three oceanic regions (including marginal basins) are defined by equal increments in the square root of crustal age: 0-25 My (A), 25-100 My (B), and > 100 My (C) and the continental regions are classified by their generalized tectonic behavior during the Phanerozoic: Phanerozoic orogenic zones (Q), Phanerozoic platforms (P), and Precambrian shields and platforms (S). Like GTR1, the oceanic regions of Mauk (1977) are based largely on crustal age. However, the continental regions of Mauk (1977) are classified by age rather than by their tectonic behavior. The more complex parameterization associated with the regionalization of Mauk (1977) does not offer us any significant advantage over GTR1; as we show through representative projections, the platform and shield signatures from the regionalization of Mauk (1977) and from GTR1 are consistent with each other and only significant at slightly better than the one-standard-deviation level. The regionalization of
Okal (1977) is limited in the accuracy of its designation of regions. For example, Okal (1977) labels the entire continent of Antarctica a shield, whereas a significant fraction (-~ 1 / 3 ) is orogenic in nature. Okal (1977) also classifies some islands (e.g., Iceland and Great Britain) as shields. Misidentifications such as these might have a significant effect on results from associated data projections. In general, a tectonic regionalization containing N distinct regions can be described by N functions, R n ( n = 1, N ) , each having unit value over its region and zero elsewhere. By combining regions, we can construct other, coarser regionalizations. For example, by consolidating young oceans (A), intermediate-age oceans (B), and old oceans (C) of GTR1, into one region, and Q, P, and S, into another region, we can create a two-component (ocean-continent) tectonic regionalization (ABC, QPS). For much of this analysis, we combine regions P and S into one region (PS). For any such regionalization, we expand each R n in spherical harmonics, omitting degrees zero and one from our analysis because geoid anomalies are referred to the center of mass and any rearrangement of mass from internal forces cannot change an object's center of mass. With coefficient R nlm representing the ( l , m ) harmonic of region n, and coefficient d Im representing the ( l , m ) harmonic of the observed
Fig. 2. (a) Geoid, l = 2-36 (EGM96; Lemoine et al., 1996), referred to the hydrostatic figure of Earth (Nakiboglu, 1982); (b) Projection of (a) onto (A, B, C, Q, PS), and (c) Residual: (a-b). All plots are displayed using a Hammer equal-area projection with coastlines drawn in white. Negative contour lines are dashed and the zero contour line is thick. The contour interval is 10 m.
140
S.S. Shapiro et a l . / Lithos 48 (1999) 135-152
Table 3 Mauk (1977) Region Oceans 1 2 3 4 5
Definition
7
Anomaly 0-5 (0-10 My) Anomaly 5 - 6 (10-20 My) Anomaly 6-13 (20-38 My) Anomaly 13-25 (38-63 My) Late Cretaceous sea floor (63-100 My) Early Cretaceous sea floor (100-140 My) Sea floor older than 140 My
Continents 8 9 10 11 12 13 14 15 16 17 18 19 20
Island arcs Shelf sediments Intermontane basin fill Mesozoic volcanics Cenozoic volcanics Cenozoic folding Mesozoic orogeny Post-Precambrian undeformed Late Paleozoic orogeny Early Paleozoic orogeny Precambrian undeformed Proterozoic shield Archaean shield
6
Fractional area (%) 61.5 4.0 10.4 6.9 10.2 21.1 5.4 3.5 38.4 1.4 7.1 0.7 0.4 1.4 1.8 2.7 9.5 1.9 1.8 1.5 6.2 2.0
(or model) geoid or gravity field, we use a leastsquares approach to solve: e/nm~n = d im
(l)
(summation convention implied here and below) for the regional averages, %. We include the additional constraint: An'Yn = 0
(2)
where A n represents the surface area spanned by region n. This constraint ensures that % have a zero (weighted) average, as, by definition, do the geoidheight (and free-air gravity) anomalies. The weighted-least-squares solution can be written:
y : [R r WR]-1Rr Wd
We next consider the effect of errors in d on our analysis. Although we have available the covafiance matrix for EGM96, this weight matrix is not the appropriate one for our analysis. As discussed previously, most of the power in the long wavelength parts of the geoid is the result not of surface tectonics, but of deep intemal processes. Unfortunately, the contribution of these deep processes cannot be determined to anywhere near the accuracy of the observed gravity field, so the covariance matrix will be swamped by the contributions of the errors due to neglecting important dynamic processes. Quantitative estimation of the errors associated with estimates of the contributions of these deep processes has rarely been attempted (Panasyuk (1998) is an exception). Here, we simply assume the identity matrix as our default weight matrix. For this matrix, the relative error in the harmonic expansion of the geoid increases as 12 (or as l for the gravity anomalies). This behavior is qualitatively consistent with the result that dynamic models of the geoid do better at fitting the longest wavelength components and progressively worse at fitting shorter wavelength components, for example, because the effects of lateral variations in viscosity become more important at shorter wavelengths (e.g., Richards and Hager, 1989). The sole exception to the identity weight matrix is our application of a large weight, 1000, to the surface-area constraint. Results from our inversions are insensitive to the value of this weight, so long as it is not less than ten times the weight associated with the data (in our case unity) nor so large ( > 106 times the data weight) that the inversion becomes numerically unstable.
(3)
where the values R/nm and A n are the elements of the matrix R, W is a weight matrix constructed from the covariance matrix associated with d, Yn are the elements of the vector y, and dtm and zero constitute the vector d.
3. Statistical analysis procedure Because neither the geoid nor the regionalization have white spectra, we do not use common statistical estimates of uncertainties. In fact, their spectra are quite red, implying that uncertainties in parameter estimates based on the assumption of white spectra will be substantially smaller than the actual uncertainties. Through the use of Monte Carlo techniques, we incorporate the spectral properties of these fields in our estimates of parameter uncertainties. For each
141
S.S. Shapiro et al./Lithos 48 (1999) 135-152
of 10,000 trials, we (1) randomly select an Euler angle triple from a parent distribution in which all orientations are equally probable and then, in accord
with the selected triple, rigidly rotate the sphere on which the data residuals (dies = d lm - R t m. y.) are defined, with respect to the sphere on which the surface
1000 0 -50
0
50
-50
0
50
-50
(m)
0
50
0
50
(m)
3000 2000
1000 _.,i
0 -50
(m)
(m)
3000 2000
1000 0 -50
0
50
0
5
10
15
20
Fig. 3. Non-hydrostatic geoid (EGM96, l = 2-36): Histograms of parameter values (a) 7A, (b) YB, (C) YC, (d) ~/Q, (e) YPs obtained from projections onto the tectonic sphere of the correlated data combined with 10,000 random orientations of the data residual sphere, characterized by a~m (see text). Gaussian distributions, determined by the standard deviation, mean, and area of each histogram, are superposed. (f) Histogram of variance reduction resulting from 10,000 random rotations of the data sphere, characterized by dtm, with respect to the tectonic sphere. The shaded and unshaded arrows indicate the variance reductions associated with the actual orientation and the maximum variance reduction, respectively.
142
S.S. Shapiro et al. / Lithos 48 (1999) 135-152
tectonics are defined ("tectonic sphere"), (2) com71m bine the rotated data residuals dre s ( " ~ " denotes rotated) with the correlated data to produce pseudo
data, ( d lm -" dre 7lms nt- Rnlm")/n)' and (3) project d Im onto (A, B, C, Q, PS). The resulting histograms of parameter values (e.g., YA, TB, YC. . . . ) approximate
1500 1000 500 0 -10
0
10
-10
0
10
0
10
-10
0
10
2000 1500 1000 500 0 -10
(regal) ,
2000
|
,
PS
1500 1000 500 0 -10
0
10
0
5
10
Fig. 4. Free-air gravity (l = 2-36): Histograms of parameter values (a) YA, (b) YB, (c) Yc, (d) ye, (e) "~PS obtained from projections onto the tectonic sphere of the correlated data combined with 10,000 random orientations of the data residual sphere, characterized by d"Tin (see text). Gaussian distributions, determined by the standard deviation, mean, and area of each histogram, are superposed. (f) Histogram of variance reduction resulting from 10,000 random rotations of the data sphere, characterized by dtm, with respect to the tectonic sphere. The shaded and unshaded arrows indicate the variance reductions associated with the actual orientation and the maximum variance reduction, respectively.
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S.S. Shapiro et a l . / Lithos 48 (1999) 135-152
Gaussian distributions and, because the correlated signal is added to the rotated data residual before projecting the composite, the resulting histograms of parameter values are centered approximately on the parameter values corresponding to the actual orientation of the "data sphere" with respect to the tectonic sphere (Figs. 3 and 4). We take these latter parameter values as our parameter estimates and the standard deviations of these approximately Gaussian distributions as the parameter uncertainties. Alternatively, we could assign random (white noise) values to each coefficient describing the data-residual sphere while constraining its power spectrum to be unchanged through a degree-by-degree scaling. Histograms resulting from this approach yield very similar distributions and virtually the same values for the parameter estimates and their standard errors (Shapiro, 1995). If one relaxes the constraint by requiring only that the total power remains unchanged, then the resulting histogram distributions are narrower than the corresponding ones for which the spectra were scaled degree-by-degree. These smaller values for the standard errors in the parameter estimates likely coincide (Shapiro, 1995) in the limit of large numbers of trials with those determined from the elements of the variance vector V ~ /~'2ost diag{[R T WR]-I}, where Xpost, : is the (postfit) X-V per degree of freedom. As a criterion for the success of the model in fitting the data, we use the percent fractional difference in the prefit and postfit X 2. This percent variance reduction associated with each projection, i.e., inversion, is thus defined by 100[1-(X2o~t/X2re)]. From the results of the random rotations of the data sphere with respect to the tectonic sphere, we estimate significance levels in the variance reduction associated with each projection. Specifically, we associate the fraction of trials that yield lower variance reductions than the actual orientation with the confidence level of the variance reduction.
4. Projections Table 4 shows the regional averages and their corresponding statistical standard errors obtained by separately projecting the geoid and the free-air gravity anomalies onto (A, B, C, Q, PS). Fig. 3a-eFig. 4 a - e graphically display the 10,000 parameter estimates obtained from the Monte Carlo simulations that lead to the uncertainties given in Table 4. With the geoid, only regions (C) and (PS) have averages which are larger than their standard errors. However, the significance of these averages is only slightly above the one-standard-deviation level. For example, with 95% (2 o-) confidence, the geoid signature associated with platforms and shields is in the range - 2 7 to + 6 m, a rather broad range which does not even significantly constrain the sign of this signal. The projection of the geoid onto (A, B, C, Q, PS) is shown in Fig. 2b and further demonstrates that very little of the long-wavelength non-hydrostatic geoid can be explained simply in terms of surface tectonics. The magnitude of the geoid signal that is uncorrelated with (A, B, C, Q, PS) (Fig. 2c) is essentially the same as that of the geoid anomalies themselves, given by EGM96. Using the free-air gravity yields a somewhat different result: four regions have averages larger than their standard errors (Fig. 4a-e). The significance of three of these averages is at or below the 1.5o- level and the significance of the fourth, TQ, is at the 2.5o- level (Table 4). With 95% confidence, the free-air gravity signature associated with platforms and shields is in the range - 1 0 to + 1.4 mgal. Like with the geoid, this range is rather large and does not significantly constrain the sign of this signal. However, unlike the geoid projection, which explains less of the variance than about two-thirds of the random orientations of the data sphere (Fig. 3f), the free-air gravity projection explains more of the variance than about 98% of projections corresponding with random orientations
Table 4 EGM96 (l = 2-36): Regional averages and statistical standard errors from projections of the geoid and of perturbations to the free-air
gravity onto (A, B, C, Q, PS) Geoid (m) Gravity (mgal)
TA
TB
"Yc
TQ
]/ps
0 _+ 12 4.0 _+3.4
1.8 + 5.6 - 1.7 + 1.7
17 _+ 16 -4.8 +_3.9
-4.8 _+11 6.4 _+2.5
- 10.5 _+8.3 -4.3 _+2.9
S.S. Shapiro et al./Lithos 48 (1999) 135-152
144
of the data sphere (Fig. 4f). However, this reduction in variance is only about 6% and does not produce an impressive fit. Interestingly, Monte Carlo simulations using degrees 2-12 yield confidence levels of less than 30%, suggesting that the association between free-air gravity anomalies and surface tectonics is stronger in the higher frequencies. Using the regionalization of Mauk (1977) (the full 20-region tectonic sphere as well as some representative groupings of these regions) leads to results similar to those obtained from GTR1. In no case do we find a significant signal that can be linked with the continental tectosphere. Combining the regions of Mauk (1977) into three groups based on crustal age (regions [1-7], [8-14, 16-17], [15, 18-20]), yields regional averages which are roughly the same magnitude as their corresponding uncertainties (Table 5) and a variance reduction of about 6%. Another continental grouping ([1-7], [8-10, 12-13], [11, 14-
Table 5 EGM96 (1 = 2-36): Regional averages and statistical standard errors from projections of the geoid onto several regionalizations based on Mauk (1977). Group 1: ([1-7], [8-14, 16-17], [15, 18-20]); Group 2: ([1-7], [8-10, 12-13], [11, 14-17], [18-20]); Group 3 : 2 0 separate regions Region
Oceans 1 2 3 4 5 6 7 Continents 8 9 10 11 12 13 14 15 16 17 18 19 20
Group 1 3, (m)
Group 2
Group 3
3' (m)
3' (m)
9• 9• 9• 9• 9• 9• 9•
9• 9• 9• 9• 9• 9• 9•
-13• 10• 9• 5• 4• 15• 40•
- 22 + 16 - 2 2 + 16 - 2 2 + 16 - 2 2 + 16 - 2 2 + 16 - 2 2 + 16 - 2 2 + 16 -7+9 -22+16 - 2 2 + 16 -7 +9 - 7+ 9 -7 +9
- 9 + 15 - 9 + 15 - 9 + 15 - 19+ 14 - 9 + 15 - 9 + 15 - 19+ 14 -19+14 -19+14 - 1 9 + 14 - 12 + 13 - 12 + 13 - 12+ 13
127 + 4 6 - 4 1 + 19 62+44 - 10+57 27+41 6+37 -34__+ 22 4+14 -61+33 -60+26 37___ 28 - 27 + 15 -23+23
17], [18-20]) based instead on a combination of age and tectonic behavior, yields similar (insignificant) results (Table 5), and even produces a slightly smaller variance reduction than the previous model, which was based on one fewer parameter. On the other hand, when one uses the full 20-region tectonic sphere, the variance reduction associated with the projection of the data sphere is about 20%. This result by itself is not particularly surprising since one would expect the variance reduction to increase with the number of model parameters. However, using this regionalization, less than 10% of our Monte Carlo simulations result in a greater reduction in variance. While this result does not allow us to reject a strong association between the geoid and the surface tectonics defined by Mauk (1977), the large relative uncertainties (and even differences in sign) associated with old continents (Table 5) suggest that this association is indeed weak. In addition, there are only three regions (8, 9, and 17) that have average values that differ from zero by more than 2 o-. Although there is substantial uncertainty in the predictions of models of the contribution of other processes to the long-wavelength geoid, perhaps we could better isolate the tectosphere's contribution by subtracting from the observed (non-hydrostatic) geoid the effects of previously modeled components" (1) a simplified representation of the upper 120 km based on the oceanic plate cooling model and a uniform 35-km-thick continental crust ( l = 2-20) (Hager, 1983); (2) the lower mantle ( l = 2-4) (Hager and Clayton, 1989); (3) slabs (l = 2-9) (Hager and Clayton, 1989); and (4) remnant glacial isostatic disequilibrium (l = 2-36) (Simons and Hager, 1997). Separately projecting each of these four contributions to the model geoid onto (A, B, C, Q, PS) yields the results given in Tables 6 and 7. Our resulting model (residual) geoid, TECT-1 (Fig. 5), provides an estimate of the contributions to the geoid of the upper mantle structure below 120 km depth, excluding subducted slabs. For TECT-1, Yr,s = -8 _ 4 m (Table 6). The projections of TECT-1 separately onto (A, B, C, Q, PS), (ABC, QPS), and (ABCQ, PS) lead to reductions in variance that are listed in Table 7. From the percent of random trials that yield smaller variance reduction than that of the actual orientation (confidence level), it is clear that the geoid signal
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S.S. Shapiro et al./Lithos 48 (1999) 135-152
Table 6 Regional averages and statistical standard errors from projections onto (A, B, C, Q, PS), corresponding to contributions to the geoid from five model geoids - - each representing a separate contribution to the geoid. The bottom two represent projections of TECT-1, separately, onto (ABC, QPS) and (ABCQ, PS) Geoid contributors
TA (m)
YB (m)
7c (m)
TQ (m)
")/PS (m)
Upper 120 km Lower Mantle Slabs Post-Glacial Rebound TECT-1
4.3 • 1.0 - 5 +_ 32 - 11 _+9 1 _+0.5 3+ 5
- 3.1 _+0.5 20 + 19 - 5 _+4 1 _+0.3 2+ 3
- 6.1 + 1.0 35 +_ 34 - 1 + 11 0.7 + 0.5 4_+6
3.1 + 0.9 - 76 _+48 21 _+ 10 -0.2 _+0.3 - 1 _+4
3.5 _+0.8 34 _+ 35 -7_+ 6 - 3 _+0.5 - 8 _+4
TECT-1/(ABC, QPS) TECT- 1/(ABCQ, PS)
2.5 + 2 1.6 + 0.8
2.5 ___2 1.6 ___0.8
2.5 + 2 1.6 + 0.8
-4 + 3 1.6 + 0.8
-4 • 3 - 8+ 4
At these w a v e l e n g t h s (l = 2 - 3 6 ) , if there were no contribution from density contrasts at depths greater than 120 km, the geoid a n o m a l y associated with isostatically c o m p e n s a t e d platforms and shields w o u l d be about + 10 m, referenced to old ocean basins, or 0 m, referenced to ocean crust of zero age or to y o u n g continental crust (e.g., Hager, 1983). Our estimate of the geoid a n o m a l y associated with old ocean basins, from the TECT-1 projections, is 4 + 6 m, for oceans 0 - 2 5 M a is 3 + 5 m, and for y o u n g continents is - 1 +__4 m. D e p e n d i n g on w h e t h e r we take old oceans, y o u n g oceans, or y o u n g continents as the reference value, our estimate of the signal due to the tectosphere alone, correcting for the effects of the crust, w o u l d be - 2 2 m, - 1 1 m, or - 7 m. B e c a u s e the old oceanic regions m a y still have some residual effect of subduction included in their estimate, and because the area-weighted average of y o u n g oceans and y o u n g continents is close to
represented by TECT-1 is, a m o n g these choices, best r e p r e s e n t e d by the t w o - r e g i o n regionalization: ( A B C Q , PS). A l t h o u g h the projection of TECT-1 onto ( A B C Q , PS) results in a variance reduction of only about 3%, this value exceeds those obtained from almost 95% of the projections associated with r a n d o m rotations of the data sphere. This result is consistent with the r o u g h l y 20- result associated with the platform and shield signal represented in TECT-1 (Table 6), but contrasts m a r k e d l y with the results for the five-region grouping (A, B, C, Q, PS), where the actual orientation of the data sphere explains m o r e of the variance than only 54% of the r a n d o m orientations. This apparent discrepancy arises because r a n d o m orientations of the other tectonic regions can " l o c k o n " to regional features in the geoid such as those associated with subduction zones, providing a better fit to the synthetic geoids globally, but not in regions spanned by the projection of PS.
Table 7 Variance reductions and the corresponding confidence levels associated with the projection onto different groups of tectonic regions of five model geoids - - each representing a separate contribution to the geoid. Confidence level represents the percent of random trials that yield a smaller reduction in variance than that of the actual orientation of each geoid contributor Geoid Contributor
Projection
Variance reduction (%)
Confidence (%)
Upper 120 km Lower Mantle Slabs Post-Glacial Rebound TECT-1
A, B, C, Q, PS A, B, C, Q, PS A, B, C, Q, PS A, B, C, Q, PS A, B, C, Q, PS
80 37 13 19 4
100 88 77 100 54
TECT- 1 TECT- 1
ABC, QPS ABCQ, PS
2 3
78 94
S.S. Shapiro et al./ Lithos 48 (1999) 135-152
146
-100 -80
-60
-40
-20
0
Meters
20
40
60
80
100
147
s.s. Shapiro et al./ Lithos 48 (1999) 135-152
zero, we retain the estimate of - 8 due to the continental tectosphere.
m as the signal
5. Estimate of ~ In p / ~ lnv s
The isostatic geoid height anomaly, g N, associated with static density anomalies can be calculated for each lateral location from (e.g., Haxby and Turcotte, 1978): -27rG gU=
~
g
f A p( z) zdz
(4)
where G is the universal gravitational constant, g is the acceleration due to gravity, and A p ( z ) is the anomalous density at depth z. The integration extends from the surface to the assumed depth of compensation. Assuming that ~ln p/i31n us is constant within a specified depth interval, we may write the scaling there between fractional perturbations in density and shear-wave velocity as:
~
~-
Olnvs
~
1
Table 8 S12_WM13 (Su et al., 1994) (/= 1-12): Platform and shield averages and uncertainties corresponding to one-way S-wave travel-time anomalies (Shapiro, 1995) Depth interval (km)
(AT/T)PS (%)
140-240 240-340 340-440
- 2.3 _ 0.2 - 1.6 _ 0.2 - 1.0 + 0.2
as the sum of the anomalies for these layers. Using the travel-time perturbations (Shapiro, 1995) (Table 8) and g Nps = Yl~S ~ - 7 . 7 + 3.9 m, we find that for platforms and shields,the average value of Oln p / O l n v s is about 0.041 ___0.021. (This estimate of standard error is based only on that of g Nps. The uncertainties associated with the regionally averaged travel-time perturbations have a much smaller effect on the value of Oln p/Olnt, s than the uncertainty associated with the geoid and are therefore ignored.)
6. Discussion
(5)
where } is obtained, for example, from the radial earth model PREM (Dziewonski and Anderson, 1981), and the fractional perturbations in shear wave velocity A vs/-~ s are equal to the negative of the fractional travel-time perturbations A~-/u for small perturbations. We base the subsequent calculation on a depth of compensation of 440 km. Below this depth, we assume that there is no platform and shield contribution to the geoid, as there is no significant distinction at such depths between the shear-wave signal beneath platforms and shields and the global average (Shapiro, 1995). Using S12_WM13 (Su et al., 1994), we calculated regional averages of one-way shear-wave travel-time perturbations for 100-km-thick layers between 140 and 440 km depth. We then approximate the integral of the depth-dependent density anomaly
None of the projections based on (1) the non-hydrostatic geoid, (2) free-air gravity anomalies, or (3) our model geoid, TECT-1, yields a platform and shield signal that is significant at a level exceeding about 2.00-. Our conclusion is in accord with that reached by Doin et al. (1996) using a geologic regionalization based on the tectonic map of Sclater et al. (1980). They estimated that shields have a geoid difference from midoceanic ridges of between - 1 0 m and 0 m; their corresponding estimate for platforms, which they keep as a separate region, is - 4 m to 1 m, while they found essentially no difference in geoid for tectonically active continental areas and ridges. They were unable to estimate formal errors because of the previously discussed red nature of the spectra, but these values represent their subjective estimates of confidence intervals. Although there are many differences in detail between
Fig. 5. (a) TECT-1, l = 2-36; (b) Projection of (a) onto (A, B, C, Q, PS), and (c) Residual: (a-b). All plots are displayed using a Hammer equal-area projection with coastlines drawn in white. Negative contour lines are dashed and the zero contour line is thick. The contour interval is 10 m.
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S.S. Shapiro et al./Lithos 48 (1999) 135-152
their study and ours, their estimates fall within our uncertainties, and their conclusion that the tectosphere is compositionally distinct is consistent with ours. These observations differ substantially from the highly significant (99% confidence) correlation, reported by Forte et al. (1995), between an ocean-continent function and the non-hydrostatic long-wavelength ( / = 2 - 8 ) geoid. However, a correlation coefficient ( r ) between different fields defined on a sphere is only meaningful (subject to tests of significance) for fields with (significantly) non-white spectra if correlation coefficients are determined separately for each spherical harmonic degree of interest (Eckhardt, 1984). Given the appropriate number of degrees of freedom associated with the correlation, one can nonetheless estimate the confidence level corresponding to the assumption that the true correlation is zero. Therefore, we estimate the effective number of degrees of freedom in the analysis of Forte et al. (1995) and, using this value, estimate the probability that the correlation which they obtained is significantly different from zero. Under the conditions outlined above, we can estimate the effective number of degrees of freedom using Student's t distribution. For uncorrelated fields, the quantity t = r[ v / ( 1 -/.2)]1/2 can be described by Student's t distribution with v degrees of freedom (e.g., Cramer, 1946; see also O'Connell, 1971). We create 10,000 degree-eight fields, each with the same spectral properties as the non-hydrostatic geoid, by randomly selecting coefficients from a uniform distribution and then scaling them degree-by-degree so that the power spectrum of each "synthetic" field matches that of the geoid. From these synthetic fields and an ocean-continent function derived from GTR1, we generate a collection of 10,000 correlation coefficients (Fig. 6a). We then estimate v by minimizing the X 2 in the fit of Student's distribution to this set of correlation coefficients (Fig. 6b). Fig. 6c,d,e
demonstrate the sensitivity of the fits to the value of v. As shown, values of v which differ from the estimated value (v = 30) by even 5 degrees of freedom, noticeably degrade the fit. The correlation coefficient corresponding to the geoid and (ABC, QPS) (l = 2 - 8 ) is - 0.18. However, using the geoid and an ocean-continent function (1 = 2-8) derived from the 5 ~ 2 155~ tectonic regionalization of Mauk (1977), we obtained the same value ( - 0 . 2 8 ) as Forte et al. (1995). With the regionalization of Mauk (1977), simulations like those described above yield 31 as the estimate of the effective number of degrees of freedom. The significance levels of the correlations associated with the GTR1 and Mauk (1977) ocean-continent functions are, respectively, about 85% and 95%. The dominant degree-two term in the geoid governs this correlation and highlights a difficulty associated with attaching significance to the correlations between such fields. For example, if one considers only degrees l = 3-8, the significance levels of the correlations associated with the GTR1 and Mauk (1977) ocean-continent functions reduce to about 55% and 60%, respectively, and hence indicate insignificant correlations. Our conclusion also differs substantially from that of Souriau and Souriau (1983) who, using a Monte Carlo scheme based on random rotations of the data sphere with respect to the tectonic sphere, found that the non-hydrostatic geoid (l = 3-12) correlates significantly (at the 95% confidence level) with the surface tectonics defined by Okal (1977). The close geoid-tectonic association obtained by Souriau and Souriau (1983) is partially related to the fact that the regionalization of Okal (1977) includes subduction zones; the association between the geoid and this regionalization is a result of the strong geoid-slab correlation (e.g., Hager, 1984). Unlike our study, Souriau and Souriau (1983)perform their projections in the spatial rather than in the spherical harmonic domain. After reproducing their results, we repeated
Fig. 6. (a) Histogram of correlations (r) between an ocean-continent function derived from GTR1 and 10,000 synthetic degree-eight fields each with the same spectral properties as the non-hydrostatic geoid. The shaded and unshaded arrows indicate the variance reductions associated with the actual geoid and the maximumvariance reduction, respectively. (b) X2, calculated from the fit of Student's t distribution with the set of t's calculated from t= r[(v/(1- r2)]1/2, plotted as a function of the number of degrees of freedom (v). The minimum value of X2 corresponds with v = 30. Histogram of values of t with Student's t distribution with v degrees of freedom superposed: (c) v = 25, (d) v = 30, and (e) v = 35.
S.S. Shapiro et al.,/ Lithos 48 (1999) 135-152
EI
9~ 1 0 0 50
-0.5
v = 25
0 -5
30
0 -5
149
S.S. Shapiro et al. ,/Lithos 48 (1999) 135-152
150
their suite of projections in the spherical-harmonic domain. We found that the correlation between the long-wavelength geoid (l = 3-12) and the regionalization of Okal (1977) is significant at about the 98% confidence level, slightly higher than the result of Souriau and Souriau (1983) of about 95% from a spatial-domain analysis. However, when we substitute a slab-residual model geoid (Hager and Clayton, 1989) for the geoid, we find that the confidence level reduces to about 50%, indicating that the signal observed by Souriau and Souriau (1983) is largely due to the correlation between slabs and the regionalization. The isopycnic hypothesis (Jordan, 1988) predicts a value of zero for Oln p / O l n v s. This value is within 2.0o- of our estimate and indicates that at this level of significance, the isopycnic hypothesis is consistent with the average geoid anomaly associated with platforms and shields. We can also estimate the value of 01np/Olnu~ by considering only thermal effects on density: Olnp
(1/p)(~p/~T)
Olnus
(l/vs)(Svs/ST)
(6)
Using a coefficient of volume expansion of 3 • 10-5 K - ~, we make two estimates" (1) Oln p/Oln us ~ 0.23, using ~ v s / ~ T ~ - 0.6 m s- ~ K - ~ from McNutt and Judge (1990) and an average upper-mantle shear velocity of ~'s--4.5 km s -1, and (2) Oln p/Olnu s 0.27, using (Olnvs/OT) ~ - 1.1 • 10 - 4 K-1 from Nataf and Ricard (1996). The average of these estimates is inconsistent at about the 10o- level with the value of Oln p/Oln us that we estimate for the continental tectosphere. Hence, our analysis indicates that a simple conversion of shear-wave velocity to density via temperature dependence is inappropriate for the continental tectosphere and that one must consider compositional effects. Our conclusion could not differ more completely from that of Pari and Peltier (1996) (henceforth PP), who claim that they can rule out the hypothesis that neutrally buoyant, compositionally distinct material exists beneath "cratons." Based on a match to the peak amplitude of a severely truncated ( / = 2-8) free-air gravity anomaly at one location (Hudson Bay), they argue that 0.21 < (Oln p/Oln vS) < 0.26, consistent with the thermal estimate above, and in-
consistent at the 8-10o- level with our estimate. However, there are several easily identifiable differences between their approach and ours. Most importantly, we use a geologic regionalization to define cratons. PP define "cratons" as any region, beneath either continents or margins, that has high inferred densities at 30 km depth in heterogeneity model S.F1.K/WM13 (Forte et al., 1994). This definition of "craton" is inappropriate for testing the composition of tectosphere for many reasons, including: (1) 30 km depth beneath continents is generally within the lower crust, not within the proposed isopycnic region of the continental tectosphere; (2) model S.F1.K/WM13 is a heterogeneity model based on a weighted fit both to the gravity field and to the seismic data, assuming that density and velocity anomalies are proportional through assumed depthdependent values of ( O l n p / O l n v s) which vary between 0.21 and 0.34 (Karato, 1993). In regions where the seismic coverage is not good, this assumption introduces a strong gravitational bias into model S.F1.K/WM13, making the use of this model in the inversion for (Olnp/Olnu s) an example of circular logic; (3) The use of this hybrid model fails to identify the South African craton, a region with thick tectosphere (e.g., Su et al., 1994), as a craton. (4) PP emphasize the value of the fit at Hudson Bay, while our study weights all regions of the globe equally. We also note that the estimate of the amount of this peak free-air gravity anomaly attributable to mantle structure is suspect due to contamination from postglacial rebound (Simons and Hager, 1997). In summary, given their approach, and their non-geologic definition of cratons, it is not surprising that PP find a different value for (Oln p/Oln vs) than we do. Their value applies to the mantle beneath regions of inferred high-density lower-crust in a model determined from a joint inversion of gravity and seismic data. Our value of ( O l n p / O l n v s) applies to cratons defined by geological processes. In summary, to obtain realistic estimates of the significance of correlations between data fields defined on a sphere requires that one consider the spectra of the data fields so that the number of degrees of freedom can be determined appropriately. Our analysis demonstrates that the relationship between the long-wavelength geoid and the ocean-continent function is tenuous. The large difference in
s.s. Shapiro et al./Lithos 48 (1999) 135-152
correlation that we obtain with different o c e a n - c o n tinent functions further illustrates its insignificance. F r o m error estimates that account for the redness in the geoid, gravity field, and tectonic regionalization spectra, we conclude that neither the geoid nor the free-air gravity has a platform and shield signal that differs significantly (20-) from zero. Additionally (see Shapiro, 1995), by considering regionally averaged shear-wave travel-time anomalies together with our m o d e l of the continental t e c t o s p h e r e ' s contribution to the geoid, we find that a l n p / a l n v S is about 0.04 _+ 0.02. A l t h o u g h this estimate is consistent at the 2.00- level with the isopycnic hypothesis of Jordan (1988), the slightly positive estimate suggests that the decreased density associated with compositional b u o y a n c y does not completely balance the increased density associated with low temperatures. W e also note that convection calculations addressing the stability and d y n a m i c s of the continental tectosphere indicate that a l n p / a l n u s is likely to vary s o m e w h a t with depth (Shapiro et al., 1999; see also Forte et al., 1995). Thus, our estimate is a weighted average of a quantity that m a y vary with position.
Acknowledgements W e thank P. Puster and G. Masters for c o m p u t e r code and T.A. Herring, P. Puster, W.L. Rodi, and M. Simons for helpful discussions. Richard J. O ' C o n n e l l provided a useful review. Figs. 1, 2 and 5 were created using the Generic M a p p i n g Tools software (Wessel and Smith, 1991). W e p e r f o r m e d m a n y of the calculations using the Guilford College Scientific C o m p u t a t i o n and Visualization Facility which was created with funds from a grant from the National Science F o u n d a t i o n ( C D A - 9 6 0 1 6 0 3 ) . This work was also supported by National Science F o u n d a t i o n grant EAR-9506427.
References Chase, C.G., 1979. Subduction, the geoid, and lower mantle convection. Nature 282, 464-468. Cramer, H., 1946. Mathematical methods of statistics. Princeton Univ. Press, Princeton. Crough, S.T., Jurdy, D.M., 1980. Subducted lithosphere, hotspots and the geoid. Earth Planet. Sci. Lett. 48, 15-22. Doin, M.-P., Fleitout, L., McKenzie, D., 1996. Geoid anomalies
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and the structure of continental and oceanic lithospheres. J. Geophys. Res. 107, 16135-16199. Dziewonski, A.M., Anderson, D.L., 1981. Preliminary reference earth model (PREM). Phys. Earth Planet. Inter. 25, 297-356. Eckhardt, D.H., 1984. Correlations between global features of terrestrial fields. Math. Geol. 16, 155-171. Forte, A.M., Dziewonski, A.M., Woodward, R.L., 1993a. Aspherical structure of the mantle, tectonic plate motions, nonhydrostatic geoid and topography of the core-mantle boundary. In: Le MouEl, J.-L., Smylie, D.E., Herring, T. (Eds.), Dynamics of the Earth's Deep Interior and Earth Rotation. Geophys. Monogr. Ser. 72. AGU, Washington, DC, 135-166. Forte, A.M., Peltier, W.R., Dziewonski, A.M., Woodward, R.L., 1993b. Dynamic surface topography: a new interpretation based upon mantle flow models derived from seismic tomography. Geophys. Res. Lett. 16, 225-228. Forte, A.M., Woodward, R.L., Dziewonski, A.M., 1994. Joint inversions of seismic and geodynamic data for models of three-dimensional mantle heterogeneity. J. Geophys. Res. 99, 21857-21877. Forte, A.M., Dziewonski, A.M., O'Connell, R.J., 1995. Continent-ocean chemical heterogeneity in the mantle based on seismic tomography. Science 268, 386-388. Gurnis, M., 1993. Comment on "Dynamic surface topography: a new interpretation based upon mantle flow models derived from seismic tomography" by A.M. Forte, W.R. Peltier, A.M. Dziewonski and R.L. Woodward. Geophys. Res. Lett. 20, 1663-1664. Hager, B.H., 1983. Global isostatic geoid anomalies for plate and boundary layer models of the lithosphere. Earth Planet. Sci. Lett. 63, 97-109. Hager, B.H., 1984. Subducted slabs and the geoid: constraint on mantle rheology and flow. J. Geophys. Res. 89, 6003-6015. Hager, B.H., Clayton, R.W., Richards, M.A., Comer, R.P., Dziewonski, A.M., 1985. Lower mantle heterogeneity, dynamic topography and the geoid. Nature 113, 541-545. Hager, B.H., Clayton, R.W., 1989. Constraints on the structure of mantle convection using seismic observations, flow models, and the geoid. In: Peltier, W.R. (Ed.), Mantle Convection, Plate Tectonics and Global Dynamics. Gordon & Breach, New York, 657-753. Hager, B.H., Richards, M.A., 1989. Long-wavelength variations in Earth's geoid: physical models and dynamical implications. Philos. Trans. R. Soc. London, Ser. A 328, 309-327. Haxby, W.F., Turcotte, D.L., 1978. On isostatic geoid anomalies. J. Geophys. Res. 83, 5473-5478. Jordan, T.H., 1975. The continental tectosphere. Rev. Geophys. Space Phys. 13, 1-12. Jordan, T.H., 1978. Composition and development of the continental tectosphere. Nature 274, 544-548. Jordan, T.H., 1981. Global tectonic regionalization for seismological data analysis. Bull. Seismol. Soc. Am. 71, 1131-1141. Jordan, T.H., 1988. Structure and formation of the continental tectosphere. J. Petrology, Special Lithosphere Issue, 11-37. Kaula, W.M., 1967. Geophysical applications of satellite determinations of the earth's gravitational field. Space Sci. Rev. 7, 769-794.
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Kaula, W.M., 1972. Global gravity and tectonics. In: Robinson, E.C. (Ed.), The Nature of the Solid Earth. McGraw-Hill, New York, 386-405. Karato, S.-I., 1993. Importance of anelasticity in the interpretation of seismic tomography. Geophys. Res. Lett. 20, 1623-1626. Lemoine, F.G. et al., 1996. The development of the NASA GSFC and NIMA joint geopotential model. Proceedings of the International Symposium on Gravity, Geoid, and Marine Geodesy. Mauk, F.J., 1977. A tectonic based Rayleigh wave group velocity model for prediction of dispersion character through ocean basins. PhD thesis, Univ. of Michigan, Ann Arbor. McNutt, M.K., Judge, A.V., 1990. The superswell and mantle dynamics beneath the south Pacific. Science 248, 969-975. Nakiboglu, S.M., 1982. Hydrostatic theory of the earth and its mechanical implications. Phys. Earth Planet. Inter. 28, 302311. Nataf, H.-C., Ricard, Y., 1996. 3SMAC: an a priori tomographic model of the upper mantle based on geophysical modeling. Phys. Earth Planet. Inter. 95, 101-222. O'Connell, R.J., 1971. Pleistocene glaciation and the viscosity of the lower mantle. Geophys. J. R. Astron. Soc. 23, 299-327. Okal, E.A., 1977. The effect of intrinsic oceanic upper-mantle heterogeneity on regionalization of long-period Rayleigh-wave phase velocities. Geophys. J. R. Astron. Soc. 49, 357-370. Panasyuk, S.V., 1998. The effect of compressibility, phase transformations, and assumed density structure on mantle viscosity inferred from Earth's gravity field. PhD Thesis, MIT. Pail, G., Peltier, W.R., 1996. The free-air gravity constraint on subcontinental mantle dynamics. J. Geophys. Res. 101, 28105-28132. Parsons, B., Richter, F.M., 1980. A relation between the driving
force and geoid anomaly associated with mid-ocean ridges. Earth Planet. Sci. Lett. 51,445-450. Richards, M.A., Engebretson, D., 1992. Large-scale mantle convection and the history of subduction. Nature 355, 437-440. Richards, M.A., Hager, B.H., 1988. The earth's geoid and the large-scale structure of mantle convection. In: Runcorn, S.K. (Ed.), The Physics of Planets. Wiley, 247-272. Richards, M.A., Hager, B.H., 1989. Effects of lateral viscosity variations on long-wavelength geoid anomalies and topography. J. Geophys. Res. 94, 10299-10313. Sclater, J.G., Jaupart, C., Galson, D., 1980. The heat flow through oceanic and continental crust and the heat loss of the Earth. Rev. Geophys. 18, 269-311. Shapiro, S.S., 1995. The stability and dynamics of the continental tectosphere. PhD Thesis, MIT. Shapiro, S.S., Hager, B.H., Jordan, T.H., 1999. Stability and dynamics of the continental tectosphere. This volume. Simons, M., Hager, B.H., 1997. Localization of the gravity field and the signature of glacial rebound. Nature 390, 500-504. Sipkin, S.A., Jordan, T.H., 1975. Lateral heterogeneity of the upper mantle determined from the travel times of ScS. J. Geophys. Res. 80, 1474-1484. Souriau, M., Souriau, A., 1983. Global tectonics and the geoid. Phys. Earth Planet. Inter. 33, 126-136. Su, W.-J., Woodward, R.L., Dziewonski, A.M., 1994. Degree 12 model of shear velocity heterogeneity in the mantle. J. Geophys. Res. 99, 6945-6980. Turcotte, D.L., McAdoo, D.C., 1979. Geoid anomalies and the thickness of the lithosphere. J. Geophys. Res. 84, 2381-2387. Wessel, P., Smith, W.H.F., 1991. Free software helps map and display data. EOS Trans. AGU 72 (441), 445-446.
LITHOS
ELSEVIER
Lithos 48 (1999) 153-170
The evolution of continental roots in numerical thermo-chemical mantle convection models including differentiation by partial melting J.H. de Smet *, A.P. van den Berg ~, N.J. Vlaar
2
Department of Theoretical Geophysics, University of Utrecht, PO Box 80.021, 3508 TA Utrecht, The Netherlands
Received 30 April 1998; received in revised form 21 January 1999; accepted 25 January 1999
Abstract
Incorporating upper mantle differentiation through decompression melting in a numerical mantle convection model, we demonstrate that a compositionally distinct root consisting of depleted peridotite can grow and remain stable during a long period of secular cooling. Our modeling results show that in a hot convecting mantle partial melting will produce a compositional layering in a relatively short time of about 50 Ma. Due to secular cooling mantle differentiation finally stops before 1 Ga. The resulting continental root remains stable on a billion year time scale due to the combined effects of its intrinsically lower density and temperature-dependent rheology. Two different parameterizations of the melting phase-diagram are used in the models. The results indicate that during the Archaean melting occurred on a significant scale in the deep regions of the upper mantle, at pressures in excess of 15 GPa. The compositional depths of continental roots extend to 400 km depending on the potential temperature and the type of phase-diagram parameterization used in the model. The results reveal a strong correlation between lateral variations of temperature and the thickness of the continental root. This shows that cold regions in cratons are stabilized by a thick depleted root. 9 1999 Elsevier Science B.V. All rights reserved. Keywords: Thermo-chemical convection; Numerical modeling; Upper mantle differentiation; Continental evolution; Partial melting; Continental root
1. I n t r o d u c t i o n
Continental nuclei are much older than oceanic lithosphere. Continents have cratonic segments with ages of 3.0 billion years and older (Condie, 1984), in contrast with the oceanic lithosphere with ages up to about 200 million years (Miiller et al., 1996). Thus,
* Corresponding author. E-mail: [email protected]; fax: + 31-30253-50-30 1 E-mail: [email protected]. 2 E-mail: [email protected].
continents apparently form stable systems in the sense that they do not subduct. Oceanic lithosphere is subducting at ocean-continent boundaries, and this process is relatively well understood. The evolution of continental systems is much less clear. In this paper, we present a model for the formation and long term evolution of continental systems within the framework of a numerical mantle convection model. There exists evidence for a specific continental configuration that extends to several hundreds of kilometers into the upper mantle. It has been suggested that the continental lithosphere, also called the
0024-4937/99/$- see front matter 9 1999 Elsevier Science B.V. All fights reserved. PII: S0024-4937(99)00028-6
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J.H. de Smet et al./Lithos 48 (1999) 153-170
tectosphere (Jordan, 1975), is a cold layer that is prevented from collapsing through a compositionally determined low intrinsic density. An overview of evidence supporting such a chemically distinct layer is given by Jordan (1988). Estimates of the depths of these chemically defined continental roots range from 200-400 km (Jordan, 1975, 1988; Anderson, 1990; Polet and Anderson, 1995; Doin et al., 1996). During the Archaean era the Earth had a hotter upper mantle because radiogenic heat production was higher and more initial heat from planetary formation and early differentiation was still stored in the Earth. It has been demonstrated that a hotter geotherm has a large effect on the depth where pressure release partial melting starts in the upper mantle (McKenzie, 1984). This melting process results in residual material with an intrinsically lower density and a basaltic crust derived from the primary melt. This low density residual material is depleted peridotite or harzburgite and its presence can explain the long term stability of ancient, i.e., > 3 Ga, continental areas through gravitationally stable compositional layering. The importance of a higher mantle temperature to the stability of oceanic and continental lithospheric systems has been discussed in Vlaar and Van Den Berg (1991), Vlaar et al. (1994) who used simple models based on the 1-D adiabatic model for partial melting by McKenzie (1984). The results of these 1-D models showed that the present day style of plate tectonics cannot be extrapolated to the Archaean, since the compositionally differentiated layers produced by a convecting mantle must have been much thicker during the Archaean. It was shown that a thick layer of harzburgitic residue underneath an also thicker crust must have led to a different thermo-chemical convection regime (Vlaar et al., 1994). In this paper, we extend these earlier models of partial melting to non-adiabatic conditions within a thermo-chemical mantle convection model (Dupeyrat et al., 1995; De Smet et al., 1998a). We use a fully dynamical numerical mantle convection model including partial melting phase-diagrams based on empirical data. A similar model has been used by De Smet et al. (1998a) and it has been further extended to investigate continental evolution. A new more realistic parameterization of the melting phase-diagram is incorporated in the present work
allowing deep melting for a realistic young Earth continental geotherm. Here, we apply this dynamic mantle differentiation model to investigate an upper mantle system subject to secular cooling in a continental setting and study in particular the formation and subsequent thermo-chemical evolution of the continental root. Other workers have investigated continental systems in the context of mantle convection models. Effects of rheology have been studied by Moresi and Solomatov (1997) and Schmeling and Bussod (1996). Effects of composition and rheology on delamination of a lithospheric root are studied by Schott and Schmeling (1998). Several authors use ad hoc compositional layering of the continental upper mantle. Lenardic (1997) uses this type of model to explain surface heat flow data. Stability aspects are examined by Doin et al. (1997). Long-term evolutions for the whole upper mantle including partial melting are examined by Ogawa (1994) and Kameyama et al. (1996). Walzer and Hendel (1997) included the lower mantle in their study of mantle evolution with respect to the chemical differentiation of heat-producing elements. The Hawaiin hotspot and rifting scenarios in relation with partially melting mantle plumes are studied by Ribe and Christensen (1994), Ebinger and Sleep (1998), and Leitch et al. (1998). In Section 2 we present our model which focuses on the Archaean continental upper mantle. Incorporated are several important physical aspects, such as adiabatic compression, viscous heating, time- and depth-dependent radiogenic heat generation, latent heat consumption, and a pressure- and temperaturedependent rheology.
2. The model
We have applied a numerical convection model for the upper mantle including pressure release melting. A similar model with a different parameterization of the melting phase diagram was applied by De Smet et al. (1998a).
2.1. Conceptual continental model Fig. 1 gives a schematic depth profile of the model. The model incorporates a crust of 30 to 50
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J.H. de Smet et a l . / Lithos 48 (1999) 153-170
z=0km z= 16km z = 30 or 50 k m
l
u p p e r crust: H c l o w e r crust: H1
d e p l e t e d mantle" H d z-250 km
u n d e p l e t e d mantle: H u
z=670 km Fig. 1. Schematic depth profile of the continental model within the left-hand column depths in km. The upper and lower crust form a high density of viscosity layer with high radiogenic heat sources. The upper part of the mantle consists of a depleted layer up to approximately 250 km depending on the mantle temperature and in the present context also depending on the type of parameterization of the melting phase diagram (see Fig. 2). This depleted layer has an intrinsically lower density ( p(F > 0) < Ps) than the deeper undepleted part of the upper mantle ( p(F = 0) = p,~). km thickness overlaying the upper mantle to a depth of 670 km, which is assumed to be mechanically decoupled from the lower mantle. The upper mantle consists of two layers: a deep lherzolitic layer of undepleted mantle peridotite and a more shallow harzburgitic layer with a variable degree of depletion. The depleted residual material is produced when the lherzolitic source material crosses its solidus and partial melting produces a melt fraction, which is assumed to be extracted instantaneously. The process of partial melting also effects the distribution of radiogenic heat sources H ( Y , t ) . Fig. 1 gives a schematic depth profile of the model
distinguishing four layers with distinct values for H(~',t). The deeper undepleted mantle has an H u = 0.09 p~W m -3, while the partial melting process reduces the value for the depleted layer to H a = 0.04 or 0.0 I~W m -3. This is due to the extraction of heat-producing incompatible elements (Walzer and Hendel, 1997). We used H~ = 0.9 p~W m -3 in the lower and H c = 4.13 ~W m - 3 in the upper crust. The values have been derived from the present day values given by O'Connell and Hager (1980) and Chapman (1986) by applying an amplification factor of two accounting for the mean radiogenic decay since the Archaean. Estimations of Archaean radiogenic heat sources vary from two to three times the present day value. We have adopted the lower bound of this density range and included a decrease of productivity through the radioactive decay constant A = 0 . 3 4 7 Ga -1, which corresponds to a half-life time of 2 Ga (Turcotte and Schubert, 1982). Three different models A to C will be discussed. Model A and B have the heat generation parameterization mentioned above, whereas Model C has zero heat generation when the degree of depletion is larger than zero, i.e., H a = 0 when F > 0 . Both Models A and B have a crustal thickness of 50 km, whereas Model C has a reduced crustal thickness of 30 km. Further differences between the Models A to C are discussed below and an overview of the model characteristics is given in Table 1. The high crustal heat generation values result in a significant crustal blanketing effect. Since the model crust also has a low density ( Pc = 3000 kg m - 3 ) and a high viscosity (Tlmax--- 10 24 Pa s) it is stably situated on top of the continental mantle. Given the constant temperature at the surface (T~rf), the shallow geotherm in the Mechanical Boundary Layer (MBL)
Table 1 Differences between models A, B and C. The last column refers to the two initial geotherms given in Fig. 2a which are both warm and cold is meant in a relative way. The heat generation density for depleted material is given in column four (Ha). All model differences are discussed in Section 2 Model
Crustal thickness (km)
Thermal coupling upper/ lower mantle
Ha (mW m- 3)
Phase-diagram parameterization
Initial geotherm
A B C
50 50 30
reservoir isolated isolated
0.04 0.04 0.0
linear polynomial polynomial
'hot' 'hot' 'cold'
J.H. de Smet et al./Lithos 48 (1999) 153-170
156
at the top of the model is to a large extend determined by its heat source distributions. In the deeper region, the geotherm is influenced by several other factors. One of them is the compositional layering. The formation of a depleted low density layer impedes large scale convection and the formation of an adiabatic mantle geotherm at this depth level. An additional factor is the rheological parameterization including a strong temperature dependence of the viscosity. The effect of cooling from the top is a strong increase of the viscosity which
gradually reduces the vigor of convection in the depleted zone which becomes stagnant from the top down. We have used a Newtonian temperature- and pressure-dependent rheology. The viscosity model follows an Arrhenius relation which, in its dimensional form, is:
~1( p,T) = ~ e x p
E+pV RT
(1)
where values are given in Table 2 and the viscosity
Table 2 Explanation of used symbols Symbols
Definition
Value
a P0 p Pc p 77 r/0
Thermal expansion coefficient Reference density Effective density p(T, F ) Crustal density at T = Tsrf Density drop upon full differentiation Non-dimensional viscosity Reference viscosity Maximum viscosity Activation energy Activation volume Gas constant Viscosity pre-factor Degree of depletion
3 • 10- 5 3416 3000 226 1021
T}max
E V R F Y T q ( X ) hor
AT Tsrf
TO T~(p) Tl(P) AT( P)sl p Ap h A K k Cp AS H H0 qb ~' Di Rb Ra
Velocity Non-dimensional temperature Heat-flow Horizontally averaged quantity X Temperature scale Surface temperature Non-dimensional surface temperature T s r f / A T Pressure-dependent solidus temperature Pressure-dependent liquidus temperature Distance between solidus and liquidus Pressure Non-dimensional hydrodynamic pressure Depth scale Radioactive decay constant Thermal diffusivity Thermal conductivity Heat capacity at constant pressure Entropy change upon melting Non-dimensional radiogenic heat generation Reference value radiogenic heat generation Viscous dissipation Internal heating number: H 0 ( h 2 ) / ( k A T ) Dissipation number: agh/cp Compositional Rayleigh number ~ p gh 3/ KrlO Thermal Rayleigh number: Po aATgh3/Krlo
10 24
250 11.0 8.3143 9 x 1011 -
Units K-1
kg m - 3 k g m -3 kg m -3 k g m -3 Pa s Pa s kJ m o l - 1 ixm 3 m o l - 1 J mol-
1 K- 1
Pa s ms
-1
Wm -2 2200 273.15 0.12416 670 0.347 10 - 6 3.416 1000 300 5.33 X 10 -6 318.4 0.1970 0.6661 • 10 6 0.6645 X 106
K K K K K Pa km (aa) -1 m 2 s-1 W m - 1 K-1 J k g - 1 K-1 J k g - 1 K-1 Wm -3 Wm -3
J.H. de Smet et al./Lithos 48 (1999) 153-170
is truncated at its maximum value "r/max = 10 24 Pa s which equates the crustal value. The viscosity prefactor ~ ' is determined from the constraint that at z = 400 km and T = 2023.15 K (i.e., 1750~ the viscosity equals the reference viscosity value r/0 = 10 21 Pas. In the present models we apply a stronger pressure dependence of the rheology, expressed in a activation volume of V = 11.0 txm 3 mol-1 compared to a V = 7.5 txm 3 mo1-1 used by De Smet et al. (1998a). Both numbers are in the range of possible values for the upper mantle (Ranalli, 1991; Karato and Wu, 1993). The increase of the pressure dependence increases the viscosity mainly in the deeper parts of the model, whereas at shallower depth the mobility increases and the zone of minimum viscosity occurs at shallower depth (z = 80 km at t = 0 in the present Models A and B). This results in a thinner MBL and an overall decrease of the geotherm of about 175 K. We consider the reduced maximum temperature in the present models to be more representative for the young Earth. The horizontally averaged geotherm for t = 0 for Models A and B used here is depicted as the thick dotted line in Fig. 2a. The thin dotted line in Fig. 2a is the colder horizontally averaged geotherm corresponding to Model C. The difference is caused by the thinner crust in Model C. In mantle peridotites subject to partial melting, the solubility of water is higher in the basaltic melt fraction than in olivine. Furthermore, hydrous olivine has a lower viscosity then anhydrous olivine. Thus, basaltic melt extraction will increase the viscosity of the residual material (Karato, 1990; Karato and Jung, 1998; Hirth and Kohlstedt, 1996). This effect can amount up to two orders of magnitude as estimated by Karato and Jung (1998). The influence of a modest increase in viscosity, i.e., the viscosity change of almost dry olivine to dry olivine, on the model has been investigated by De Smet et al. (1998a). It stabilizes the root further and increases the thermal blanketing effect slightly. The initial geotherm has been computed from the resulting temperature field obtained from a startup convection run. In this startup run, partial melting and the decrease of heat production in time are artificially switched off. After several hundred million years a statistically steady-state sets in, and a single snapshot of the temperature field of this
157
Fig. 2. Parameterizations used in the models. (a) The thick lines are the solidus and liquidus for the linear (dashed) and polynomial (solid) parameterization where S and L indicate the solidus and liquidus for both parameterizations, respectively. The thinner lines correspond with phase equilibrium lines for which a degree of depletion is reached of 30% and 60%. The kink at 15 GPa corresponds to the phase transition that takes place at this depth. The thick dotted line is the initial geotherm at which melting is switched on at t -- 0 for Models A and B. For Model C, this is the thin dotted line. (b) (inset), degree of depletion ( F ) as function of normalized super-solidus temperature 0 for the two models. The linearized curve (dashed) is a simplification of data given by Jacques and Green (1980) and corresponds with the dashed phase-lines of Fig. 2a. The bent curve (solid) is the third-order polynomial fit as determined by McKenzie and Bickle (1988) and is used in the phase-diagram given by the curved phase-lines of Fig. 2a. The dots correspond to F-values of 0, 30, 60 and 100% and for which the phase lines are given in Fig. 2a.
steady-state is used as an initial condition for a subsequent model run including partial melting and decrease of radiogenic heat production with time. We refer to previous work (De Smet et al., 1998a) for a more extensive discussion.
2.2. Parameterization of the partial melting process Mantle differentiation through partial melting is implemented in our model based on a melting
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J.H. de Smet et al./Lithos 48 (1999) 153-170
phase-diagram for peridotite, which gives the equilibrium value of degree of depletion F for given values of p and T. In previous work (De Smet et al., 1998a) we have used a simple parameterization of the phase-diagram, using linear and parallel curves for solidus and liquidus (Takahashi and Kushiro, 1983). Here, we also apply an improved parameterization based on a higher order polynomial fit of empirical data for the solidus and liquidus of mantle peridotite. Solidus and liquidus lines for both parameterizations are shown in Fig. 2a labeled with S and L, both the linear (dashed lines) and the polynomial (solid lines) parameterizations are shown. Up to 15 GPa the curved solidus and liquidus are third-order fits to data from Gasparik (1990) and Takahashi (1990) also used by Vlaar et al. (1994). For pressures in excess of 15 GPa, a second-order fit to the data from Ohtani et al. (1986) has been applied. The sample material used in both references are not identical and therefore a constant shift of about - 7 0 K has been applied to the data points from Ohtani et al. (1986) such that solidus and liquidus are continuous at p - 15 GPa. With /~= (1,p,p2,p3)r the parameterization used for the solidus is:
rs(p) as - ( 1136, 134.2, - 6 . 5 8 1 , 0 . 1054)r 9 p _< 15 GPa as = (1510.76, 46.27 , - 0.8036, 0.0) r 9 p > 15 GPa
(2) where superscript T is the transposed of the vector. For the liquidus we used: r , ( p ) = a~/~ a~ - ( 1762, 57.46, - 3.487 , 0.0769)r 9 p _< 15 GPa d t - (1470.3025,55.53, - 0 . 9 0 8 4 , 0.0)r. p > 15 GPa
(3) From Fig. 2 we conclude that up to 5 GPa and near the solidus (indicated with S in Fig. 2a) both parameterizations are similar. However, for the larger part of the phase-diagram the differences are significant. Deep melting processes for pressure values exceeding 10 GPa, for example, are excluded by the
linear parameterization for realistic geotherms. Also, the polynomial parameterization is combined with a more realistic parameterization of depletion dependency on the normalized super-solidus temperature 0 given by:
f(p,r) =f
zlT~l(p) =/(0)
(4)
where symbol definitions are given in Table 2. We adopted an empirical relation for f ( 0 ) as given by McKenzie and Bickle (1988), which is based on a third order polynomial fit of available empirical data. In Fig. 2b, this relation is represented by the solid curve and the dash-dotted line is the linear relation used by De Smet et al. (1998a), a linear fit derived from data given by Jacques and Green (1980). The dots on the curves correspond to different degrees of depletion (30%, 60%) for which the equilibrium phase lines are drawn in Fig. 2a. The different phase diagrams result in a different distribution of partial melting. In particular, the more realistic curved solidus will result in melt production at greater depths. The differences in the phase diagrams result in different dynamics of the model. This is caused mainly by the corresponding differences in the compositional buoyancy defined in terms of F and in the differences in latent heat consumption during partial melting. The density effecting the buoyancy is given by the linearized equation of state:
p(T,F) = p0[1 - o ~ ( T - Tsrf)
-
-
f6p/po]
(5)
The EOS (Eq. (5)) includes a linear fit of empirical data specifying p(F) from Jordan (1979), where 8p is given in Table 2. In the present work, two sets of modeling results are discussed which differ in the type of parameterization of the melting phase-diagram. Model A uses the linearized parameterization and Model B and C are based on the higher order polynomial parameterization.
2.3. Thermal coupling between upper and lower mantle For secular cooling models of the upper mantle, thermal coupling between upper and lower mantle is important. Here, we consider two limiting cases implemented in the aforementioned Models A to C.
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Model A includes a simple heat reservoir representing the lower mantle which is assumed isothermal T = TR(t) as used by Kameyama et al. (1996). The reservoir does not contain any internal heating. Its volume is twice the volume of the upper mantle and other physical properties equal those of the upper mantle. The heat extracted from the reservoir is computed from the heat flux through the lower boundary of the numerical model, i.e., the upper/lower mantle interface. The reservoir temperature is used as a time-dependent essential boundary condition in Model A. In Models B and C we consider an upper mantle thermally isolated from the lower mantle. With the heat reservoir approximation we establish a more realistic estimate of the effect of a non-zero heat flow from the lower mantle. Models with a zero heat flux condition at the bottom boundary can be considered as end-member cases, which result in a maximum estimate of the cooling rates of secular cooling of the upper mantle system (De Smet et al., 1998a).
2.4. Governing model equations and numerical methods In the following equations, non-dimensional quantities are used unless explicitly stated otherwise. We used a non-dimensionalization scheme described by Van Den Berg et al. (1993). For an infinite-Prandtl-number fluid, the momentum equation with the thermal and compositional Rayleigh numbers Ra and R b respectively, is given by:
V(rI(VY+ VYr)) - V A p = ( R a T + R b F ) ~
(6)
where ~ is the unit vector in the vertical direction aligned with gravity. The definitions of the symbols are listed in Table 2. The transport equation describing partial melting of a volume of mantle material in terms of the degree of depletion F is"
d F(p,T) dt
=
df( 0 ) dt
(7)
where the right-hand-side describes a source distribution of partial melt production following from the phase diagram discussed above. Recurrent melting is
incorporated in this formulation, meaning that a volume of recycled partially melted material experiences further melting when its super-solidus temperature 0 is in excess of any previously reached value. The energy equation used is based on the Extended Boussinesq Approximation (EBA) (Ita and King, 1994): dT dt
D i ( T + T0)uz-- V Z T + ~ H ( z , t ) Di
AS d F
Ra
Cp
+ - - a s - (T+
dt
(8) where the symbols are defined in Table 2. The last three terms of the right-hand-side are: the radioactive heat generation, viscous dissipation, and latent heat consumption. The second term on the left accounts for cooling and heating due to adiabatic (de-)compression. The effect of viscous heating is relatively small since the vigor of convection is low after the depleted layer has formed. The momentum and energy equations are solved with a finite element method (Van Den Berg et al., 1993) and a time-dependent upwind scheme (SUPG) (Hughes and Brooks, 1979; Segal, 1982) is applied to the latter to improve numerical stability in advection dominated regions of the domain. The transport equation for F is solved using a Method of Characteristics (MoC) (Sotin and Parmentier, 1989; Sparks and Parmentier, 1993). A hybrid scheme using both low and high order interpolations for F in combination with a fourth order Runge-Kutta time-integration for the integration part was applied over a structured grid (De Smet et al., 1998b). In order to limit the amount of numerical diffusion over the whole domain, this unequally spaced grid used for the MoC computations of the degree of depletion field F was much denser than the finite element mesh used, and the grid densities were higher than those used by De Smet et al. (1998a). We used a resolution with grid cells ranging from 1121 to 3116 m in the horizontal direction and 921 to 1688 m in the vertical direction. A Predictor-Corrector timestepping scheme is applied to solve the Equations in the following order: Eqs. (6)-(8).
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J.H. de Smet et al./Lithos 48 (1999) 153-170
3. Numerical modeling results We will focus mainly on the differences in the evolution of Models A and B. Results for Model A are qualitatively similar to earlier results described by De Smet et al. (1998a). The increase of the activation volume in our present models results in a colder geotherm due to a thinner MBL. Up to approximately 200 Ma both models A and B show a similar evolution pattern. After this time deep upper mantle differentiation starts to occur in Model B. We first discuss the early stage before the onset of deep melting in Model B. Next we describe the long term evolution of the continental model with special interest in the stability of the system. A brief description of the dynamically created initial condition has been given above.
3.1. Early evolution From Fig. 3a and 3b a global comparison between model A and B can be made. In the left column the compositional field (degree of depletion F) is shown with upper (white) and lower (black) crustal layers on top of the partially depleted layer shown in color. The lateral variation of the temperature field with respect to the horizontally averaged background value, i.e., T - ( T ) h o r , is shown in the right-hand column. All frames also contain instantaneous flow lines indicating clock- and counterclockwise flows as black and white contour lines respectively. The advection velocities in Model A are higher than those in Model B as can be seen from the number of flow lines within each convection cell. This is mainly due to the differences in the accumulated depleted layers resulting from the different melting parameterizations as will be shown below. The small down-wellings of material with low degree of depletion of < 10% (light-blue to white) in Fig. 3.b.2 are due to re-mixing as will be discussed together with the long term evolution. The lateral temperature variations are similar for both models, with exception of the high T-anomaly above the up-welling part of the convecting cells in Fig. 3a2. This large scale two-cell convection pattern is persistent during a long period of the model
evolution. Fig. 3a and 3b illustrate the relatively short time scale of < 100 Ma in which a compositionally distinct continental root builds up in a convecting mantle after the onset of melting at t = 0. This shows that mantle differentiation is a powerful process in a planetary mantle which is hot enough for the mantle adiabat to intersect the solidus. The rapid build-up of a stably layered system results in a reduced heat transport efficiency and a gradual warming of the deeper half of the model. Fig. 4 shows the depth distribution of several horizontally averaged quantities for four time values after the onset of melting for both Model A (Fig. 4a) and B (Fig. 4b). Frames numbered 1 through 4 correspond to (1) degree of depletion F, (2) temperature T, (3) viscosity ~q(p,T), and (4) root-meansquared velocity Vrms. The averaged profiles for F (Fig. 4al and 4bl) indicate that both models initially evolve in a similar way. The continental root grows due to the mechanism of intermittent small scale diapiric melting events as investigated by De Smet et al. (1998a,b) where the parameterization of Model A was used. The same mechanism is operative in Model B. The depleted layer in model B (Fig. 3bFig. 4b l) is thicker than in Model A where melting occurs in a greater depth interval. This is clearly shown by the difference in pressure where the initial geotherm intersects the solidus lines in Fig. 2a. This pressure difference is about 1 GPa and results after 100 Ma in a continental root extending to approximately 180 and 220 km for model A and B, respectively. Note also the finite values of F in the 350 to 500 km depth range after 200 Ma in Model B (Fig. 4bl). Due to the different F(0)-parameterizations, the transition from the depleted root to the deeper undepleted mantle is sharper, i.e., the slope of (F)hor is steeper for Model B (Fig. 4b 1) than in Model A (Fig. 4.a.1). Note that the maxima of (F)hor are in both cases practically identical. This is explained by the fact that for a 0 of about 0.25, an F-value of about 30% is obtained in both F(O) parameterizations. This is indicated by the proximity of 0 values of the two dots for F = 30% in Fig. 2b. Fig. 4a2, 4b2 show the horizontally averaged geotherms. Both models show an initial increase of temperature with time in the deeper half of the model. This is a result of the rapid build up of a
161
J.H. de Smet et al./Lithos 48 (1999) 153-170
I
. . . .
I
500
. . . .
I
1000
'
'
~
"
i
'
" '~' '"
1500
Fig. 3. The depletion field and lateral variations of the temperature field (i.e., g T = T - { T ) h o r ) at 100 Ma and 200 Ma for both parameterizations of the phase-diagram. Figures labeled a and b correspond to Models A and B, respectively. Black and white contour lines indicate clock and counter clockwise flows, respectively. White F-field contouring corresponds to 9% < F < 10%. The depletion for the polynomial case is larger than in the linear case due to the different F-dependency of 0 (see the inset Fig. 2b). Also the thickness of the depleted layer is slightly thicker when the curved solidus/liquidus are used.
shallow layering inhibiting whole layer upper mantle circulation. This layering consists of cold, and therefore strong material which is part of the MBL. This cold and depleted layer is gravitationally stable with
respect to the deeper parts of the model. A superadiabatic regime develops quickly in this stagnant top layer, indicating the predominance of conductive heat transport over advection. In Model B, the
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J.H. de Smet et al./Lithos 48 (1999) 153-170
~q
li
Fig. 4. For all cases shown in Figs. 3 and 5 horizontally averaged profiles are given: (1) the degree of depletion, (2) the temperature, (3) the viscosity, (4) and the velocity root mean square. The dashed curves in (a2) and (b2) are the solidus and liquidus. Note the numerical instabilities in the ( F)-profile for t = 700 Ma in Model B (b 1), which is caused by the too coarse grid over which the transport equation for F is solved. These wiggles are also expressed by the wash-board effect in Fig. 5b2.
geotherm intersects the solidus at large depths at t ~ 200 Ma and melting is initiated in the lower half of the domain. The latent heat effects of the endothermic phase transition from olivine to spinel at 15 GPa may prevent the geotherm from crossing the solidus above 15 GPa. However, solid-state phase transitions are not included in the present models. After several hundred million years ( ~ 300 Ma) the temperature at the bottom of the upper mantle starts to decrease. These results illustrate the thermal blanketing effect of layered continental systems (Gurnis, 1988), which delay secular cooling. This decrease of the bottom temperature is stronger in Model B, because of the absence of heat influx from the lower mantle, and because latent heat consumption and surface heat flow are higher in Model B.
In Fig. 4a3,b3 viscosity profiles are shown, the crustal viscosity is set by the truncation value ~max ---~ 10 24 Pa s applied for numerical reasons. Effects of initial warming at large depth and cooling from the top are reflected in the temperature-dependent viscosity. Model A develops a viscosity minimum which is slightly more pronounced and at shallower depth than Model B. In Fig. 4a4,b4 we show the Vrm s distribution based on horizontal averaging. Model B shows a strongly reduced vigor of convection in the top half of the model. This is explained by the fact that the low viscosity zone in Model A is effectively positioned below the depleted layer resulting in a relatively mobile top layer of the undepleted mantle. In Model B the low viscosity zone occupies a depth
J.H. de Smet et al. ,/Lithos 48 (1999) 153-170
range with finite value of the degree of depletion F, reducing the vigor of convection.
3.2. Long-term evolution Fig. 4al,bl show that models A and B have a different long-term evolution. In Model A the thickness and volume of the continental root gradually increases with time due to the melting events in the upward flow of the two cell convection pattern which persists in the deep undepleted zone. At the sites of the down-wellings depleted material is slowly dragged into the lower half of the model. A low degree of depletion of about 2% volume average is found in this lower half. In Model B much further depleted material is found in this deep region. Only a small part of it originates from re-mixed depleted material. Most of it is formed at depth since the geotherm has reached and crossed the solidus after about 200 Ma of evolution as shown in Fig. 4.b.2. This results in modest but steady partial melting during the time-span from t = 200 Ma to 850 Ma. The wiggles in F shown in Fig. 4bl below 450 km depth are due to the limited grid resolution in the lower part of the model. Fig. 4a2,b2 show the evolution of the geotherm for Models A and B, respectively. In Model B, the geotherm is stabilized close to solidus at large depths (i.e., p > 15 GPa) during the initial warming stage. This is the result of the occurrence of deep partial melting and the associated latent heat consumption at these depths. In Model A, the averaged temperature at 670 km is steadily increasing and is not bounded by partial melting. Due to shallower melting events the root is growing steadily and conductive heat transport slowly becomes more dominant than advection. The geotherms in Fig. 4a2,b2 also show when the heat reservoir approach is used, i.e., Model A, the inflow of heat from the lower mantle is very small. We therefore conclude that the differences in the results of Models A and B are mainly due to the difference in the phase-diagrams and to a lesser extent to the different thermal coupling with the lower mantle. Fig. 4a3,b3 show the corresponding viscosity profiles during the evolution. In Model B the viscosity at large depths reaches an almost stationary value after 200 Ma since the geotherm be-
163
comes almost stationary. As secular cooling proceeds the MBL at the top grows and the minimum viscosity value increases and its position slowly shifts from 200 to 300 km depth during the 200 to 700 Ma time-span. Model A has a less thick depleted top layer and advection rates are higher than in Model B. This results in a hotter geotherm in the root and a smaller viscosity minimum. These differences in geotherm evolution combined with a different evolution of the buoyant zone result in different convection velocity profiles shown in Fig. 4a4,b4. Fig. 4a4 shows that the vigor of convection in Model A has increased near the bottom of the depleted root. This indicates active melting and corresponding production of buoyant residual material. The thickness of the continental root grows accordingly (Fig. 4al). After 200 Ma velocities decrease as an effect of cooling from the top and a corresponding increase of the viscosity, shown in (Fig. 4a3). Fig. 4b4 shows a downward shift of the velocity maximum and an increase of velocity at greater depth which coincides with the onset of deep melting around 200 Ma. If we define that the transition from root to underlying mantle is situated at approximately F = 0.1, we see that at 700 Ma the continental root in Model B has grown to about 400 km thickness with large lateral variations (Fig. 5). Convection velocities start to increase again while the melt production in the deep layer ( p > 15 GPa) continues. Calculations for Model B were stopped at 850 Ma because the insufficient resolution in the bottom layer and corresponding oscillations in the F-field solutions produce increasingly unreliable results beyond that time. Fig. 5a and 5b are contour plots of the depletion and temperature fields for Models A and B, respectively. These snapshots correspond to the profiles as given in Fig. 4, i.e., 400 and 700 Ma. For Model A also the snapshot at t = 1200 Ma is given. In Model A the pattern of convection changes from a relatively vigorous two-cell pattern at 400 Ma to a multi-cell convection regime at 700 Ma, in line with the observed (Vrms >hor profiles discussed above (Fig. 4a4). Melting has stopped at ~ 650 Ma, so the depletion F is subject to advection only from that time on. Both snapshots of Model A show structures of depleted material with depletion values up to 10%
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J.H. de Smet et al./Lithos 48 (1999) 153-170
j
n
1000
]
I
I
'
!
!
,I
I
Fig. 5. As in Fig. 3 but now for t = 400, 700 Ma and for Model A also at 1200 Ma. Figures labeled (a) and (b) correspond to Models A and B, respectively. Due to melting at large depths in Model B the lower half of the domain is also depleted. The wash-board effects visible in the degree of depletion of Fig. 3b2 are numerical instabilities caused by the MoC-method applied over the too coarse grid in this lower part of the domain.
J.H. de Smet et al./Lithos 48 (1999) 153-170
(white), which are dragged down into the undepleted zone. This process contaminates the deeper regions with depleted material at very slow rates. At t = 1200 Ma (Fig. 5a3) there is a small thread-like structure of depleted material (green, i.e., F ~ 15%) delaminating at x = 1000 km. Fig. 5a3 shows more stream-lines at t = 1200 Ma than Fig. 5a2 at t = 700 Ma, indicating that convection rates have increased over this time interval. This is caused by continued cooling form the top, which slowly increases the temperature difference across the deeper undepleted layer and increases convection rates. It also neutralizes the positive compositional buoyancy of the deep part of the continental root, which allows for intermittent small scale delamination (Fig. 5a3). At the same time, however, the MBL extends to larger depths due to the cooling from the top (Fig. 4a3), which prevents the gross part of the root from sinking into the slowly convecting undepleted layer. The lateral temperature variations shown in Fig. 5al,a2 also express the change in convection style. The high T-anomaly above the ascending flow in the two-cell convection decreases from t = 400 to 700 Ma. Fig. 5bl,b2 show the same snapshots for Model B. The scarcity of the streamlines illustrates that the vigor of convection is much lower compared to Model A, which is in line with the 1-D velocity profiles shown in Fig. 4b4. The differences in the depletion fields between Models A and B are large due to the ongoing deep melt production in the latter. This is illustrated by the large amount of depleted material with F > 10% (white = 10%) advected by the convection in the deep zone. Ongoing melt production keeps adding residual material in the continental root which grows to a depth of about 400 km. The 'wash-boarding' effect in the low depletion zone (light blue to white) correspond to the wiggles already described in the 1-D profiles in Fig. 4bl. In Fig. 5a3, no 'wash-boarding' is observed since the used resolution is much higher in the lower part of the domain in Model A than in Model B. The amplitude of the temperature anomalies in Model B increase from t = 400 to 700 Ma as shown in Fig. 5bl and 5b2. This coincides with a temporal acceleration of the convective flow at about t = 700 Ma, related to the up-welling near x = 1000 km and
165
downward flow at x = 500 and 1500 km. The temperature anomalies shown in the fight-hand column correlate with the distribution of composition and the structure of the convective flow. The depleted compositional root is generally cold with the exception of young newly formed residual material in up-welling flow. Both the spatial variations of depletion and of the temperature field are reflected in the geophysical observables: the seismic wave velocity structure of continental areas as revealed by surface wave tomography (Muyzert, 1996; Curtis et al., 1998), wave velocity patterns (Jordan, 1975; Anderson, 1990), and the shear wave velocity distribution on a global scale (Zhang and Tanimoto, 1993), and in the observed gravity field over continental areas (Matyska, 1994; Doin et al., 1996).
3.3. Patterns of mantle differentiation Fig. 6al and 6bl show the evolution of the melt production accumulated over columns in the models as a function of the x-location and the evolution of this melting pattern. The first 50 Ma of the evolution corresponds to the initial phase of rapid differentiation immediately following the onset of melting at t = 0. During this initial period most of the continental root is formed in our model. The figures show that most of the melt is formed in vertical columns with a steady position at the location of warm upwellings in the large-scale convection pattern of the deep mantle shown in Fig. 3. Fig. 6a2,b2 show the evolution accumulated over rows of the computational domain. These frames illustrate the evolution of the melt generation at different depths. Melt production occurs in a wider range for Model B as a consequence of the different shape of the peridotite solidus (Fig. 2a). Deep melt production for p > 15 GPa starts around 200 Ma in Model B (see Fig. 6b) and continues until the end of the computation at 850 Ma. The deep melting has a less pulsating character in time because this type of melting does not take place in rapid vertical ascending flows. Melt generation is concentrated at 600 km depth and near the kink of the phase equilibrium at 448 km depth, i.e., at p = 15 GPa. This is explained by the way in which the almost adiabatic deep geotherm intersects the curved solidus in the this part of the model. The large
166
de Smet et al./Lithos 48 (1999) 153-170
al
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'''l
....
I ....
I ....
I
....
I~
[ J
,;
-
|
400
-
I
....
t ....
t , . ...... I. . . . . .
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I
b2 100
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200 -
..... '+.... " '
l
._~ 300 c...
~. 4oo "o 500 600
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-
|
....
-
t . . . . [ . . . . I . . . . I,,,I,I
Fig. 6. The horizontal ( a l - c l ) and the 1-D depth ( a 2 - c 2 ) melt production distribution as a function of time for Model A, B and C. Figures labeled (a), (b) and (c) correspond to Models A, B and C, respectively. Note the large difference in partial melting depths for both cases. In (b2) and (c2), the solid line is the depth where the 15 GPa kink in the solidus is located. The dashed vertical lines indicate the time where computations have been stopped. Model calculations for Model A exceed the here given time-window.
melting event between 200-300 km depth at 700 Ma shown in (Fig. 6b2) is reflected in the F- and T-fields shown in (Fig. 5b2). The same melt production plots for Model C are given in Fig. 6cl,c2. Model C has the same phasediagram parameterization as Model B, but no deep melting occurs due to the lower potential temperature and the lower density of heat generating elements. The pattern of melting is therefore similar as in Model A and differentiation takes place at pressures lower than 10 GPa. The depth range is, however, larger than in Model A and extends to a maximum of 250 km. When cooling proceeds, melting ceases as in Model A, although in Model C melting proceeds longer than in Model A. A 3-D extension of the 2-D model will not alter the observed processes to a great extend. On the one
hand, a cylindric type of upwelling in a 3-D model will probably melt further since it can penetrate more easily into the existing root. On the other hand, excess heat contained in the diapir is also lost more rapid in a cylindric configuration, which results in more modest degrees of melting. 3.4. Global evolution
Fig. 7 shows several globally averaged quantities for Models A, B and C, denoted by short dashed, solid, and long dashed lines respectively. The first - 1 5 0 to 0 Ma show the statistically steady-state of the start-up scenario during which partial melting and decay of radioactive heat sources is switched off. Melting is allowed for times larger than t = 0 Ma, when radioactive decay starts. This results in the
J.H. de Smet et al./Lithos 48 (1999) 153-170
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....
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I'''
C 3.0 ~ ' 2.5
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. . . .
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88 , , , l J , , , l , l l l l l j L ~ [ l l l ~
d
E ......
I .... i''"1 .... I .... I .... i"
A
v
60
,i
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Fig. 7. For both models the evolution of some volume averaged quantities are given. The results for Model A, B and C drawn with short dashed, solid, and long dashed lines, respectively. Volume averages of the following quantities are depicted: (a) temperature, (b) degree of depletion, (c) velocity root-mean-square (Model C not shown). The averaged surface heat flow number is depicted in (d).
short period of about 50 Ma of extensive differentiation illustrated also in Fig. 6, during which a large part of the continental root is formed. The rapid initial formation is an artifact of the particular start scenario used. Subsequent evolution however shows more realistic aspects of the model. The volume averaged temperature shown in Fig. 7a diverges between Model A and B, especially from about 200 Ma onwards. This is mainly due to the effect of latent heat consumption, which increases strongly at the onset of deep melt production in Model B. The secular cooling shown in Fig. 7a is
167
mainly due to conductive cooling from the top, since deeper parts of the model experience an initial warming during several hundred million years as shown in the evolution of vertical profiles in Fig. 4. Model C has an averaged initial temperature which is 70 K lower than in Models A and B. After the onset of melting, owing to the reduced heat production, the temperature in Model C drops much faster than in the two others. Fig. 7b shows the volume average of the degree of depletion. The initial phase of rapid melting is reflected in the steep increase of < F ) . In Model B, more melt is produced and melting continues until the end of the computations whereas in Model A, melting ceases around t = 650 Ma. Model C produces approximately the same volume of continental root as Model A which is explained by the difference in phase-diagram parameterization: in spite of the colder geotherm it can still generate a large amount of depleted material. Fig. 7c shows the root mean squared velocity Vrms based on the volume average. After an initial spike shortly after t - 0 of 5 cm a-1 for Models A and B, truncated in the time series plot, the < VrmS) drops from 2.8 cm a-a during the statistically steady-state before the onset of melting to a value lower than 1 cm a-1. Small local maxima correspond to pulsating diapiric events which also coincide with small shifts in the time series of < F ) (i.e., increasing) and
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J.H. de Smet et al. / Lithos 48 (1999) 153-170
The bottom part of the model forms a relatively slowly convecting layer, and therefore has no pronounced Thermal Boundary Layer (TBL) (Fig. 4a4). Heat flow density through the Earth's surface is shown in Fig. 7d. Values decrease considerably after the formation of a stable continental root that prevents whole layer convection. During later evolution the strong MBL grows from the top down and a more conductive regime, with reduced heat flow, develops. The increase in ( q ) for Model B corresponds to the acceleration in the convective heat flow at approximately t = 700 Ma discussed above. The heat influx from the lower mantle in Model A is less than 7.5% of the heat outflow through the surface, whereas Model B has a zero heatflow contribution from the lower mantle. Nevertheless, the surface heat flow in Model B is slightly higher than in Model A. This is due to the modestly higher advection rates in the very shallow part of the root in Model B compared to Model A (Fig. 4a4,b4), which transports heat more efficiently through this thin shallow layer. Continental heat flow values range between approximately 25 and 75 mW m -2 at present for cratons (Pollack et al., 1993) and the here observed values should reach this range after approximately 2 to 3 Ga which is reasonable. Model C follows Model A but with an approximately constant heat flux difference of 15 to 20 mW m -2. This is mainly due to the reduced radiogenic heat production in the crust of Model C.
4. Concluding remarks Our numerical modeling results show that a hot convecting mantle will produce a compositional layering which is similar to the layered model of the continental tectosphere (Jordan, 1975). It is found that this layering remains stable on a time scale greater than one billion years. These results support the conclusion that present-day cratonic continental roots revealed by seismology are relicts of a hotter Archaean mantle. We have investigated different parameterizations of the melting phase diagram of mantle peridotite. For the more realistic parameterization, we found an increase in melt production which also occurs over a larger depth range, compared to the simpler linear parameterization. This model also shows significant
partial melting in the transition zone of the upper mantle ( p > 15 Gpa), for a sufficiently high initial potential temperature (Model B). This model needs to be explored further in the future. In particular the solid state exothermic phase transition near 400 km depth and the associated latent heat effects on warm diapiric up-wellings and the occurrence of deep melting requires further investigation. Simulations with a simple melting phase diagram show a compositional layering that becomes more pronounced until partial melting stops at about 650 Ma, which result from a progressive secular cooling that eventually brings the average geotherm below the solidus. This resulting layering remains stable for the duration of the computations (1400 Ma), but some small-scale delamination of the continental root and re-mixing of depleted material is observed. In the interpretation of the observed long-term stability of the continental layering, we should keep in mind some limitations of the model. In the real Earth, continents break up. This may be related to the interaction of large scale mantle plumes with continental roots and a certain degree of freedom for continental blocks to migrate laterally (Ebinger and Sleep, 1998). In our model, lateral migration is limited by the symmetry condition applied on the vertical boundaries of the computational domain. At the same time, only relatively small mantle diapirs interact with the continental root and they cannot sufficiently affect the root to result in continental break up. The continental root grows by means of relatively small scale diapiric up-wellings which cross the solidus near the lower boundary of the root. These diapiric flows are then accelerated by the density reduction effect of the partial melting process on the residual matrix, resulting in a positive buoyancy which dominates the effects of latent heat consumption and adiabatic decompression, both included in our models. The amount of melt produced in a single diapiric event is significantly smaller than the estimated amounts produced during events that are related to continental flood basalts. A clear correlation was found between lateral variations of the temperature and of the thickness of the continental root. Cold areas coincide with an increased thickness of the root and warm areas show a thinned root.
J.H. de Smet et al./Lithos 48 (1999) 153-170
Acknowledgements We thank Shijie Zhong and Rob van der Hilst for critical reviews which helped to improve the manuscript. We acknowledge stimulating discussions with David Yuen. This work was partly supported by the Netherlands Organization for Scientific Research (NWO) and the Dr. Schiirmann foundation through travel grants and was partly carried out during a visit of Jeroen de Smet and Arie van den Berg at the Minnesota Supercomputer Institute. Support was also received from the Netherlands Science Foundation (NWO) and NATO.
References Anderson, D.L., 1990. Geophysics of the continental mantle: a historical perspective. In: Menzies, M. (Ed.), Continental Mantle. Oxford, United Kingdom, Clarendon Press, pp. 1-30. Chapman, D.S., 1986. Thermal gradients in the continental crust. In: Dawson, J.B., Carswell, D.A., Hall, J., Wedepohl, K.H. (Eds.), The Nature of the Lower Continental Crust. Vol. 24, Spec. Publ. Geol. Soc. London, pp. 63-70. Condie, K.C., 1984. Archaean geotherms and supra crustal assemblages. Tectonophysics 105, 29-41. Curtis, A., Dost, B., Trampert, J., Snieder, R., 1998. Eurasian fundamental mode surface wave phase velocities and their relationship with tectonic features. J. Geophys. Res. 103, 26919-26947. De Smet, J.H., Van Den Berg, A.P., Vlaar, N.J., 1998a. Stability and growth of continental shields in mantle convection models including recurrent melt production. Tectonophysics 296, 1529. De Smet, J.H., Van Den Berg, A.P., Vlaar, N.J., 1998b. A characteristic based method for solving the transport equation and its application to the process of mantle differentiation and continental root growth (submitted to Geoph. J. Int.). Doin, M.-P., Fleitout, L., Christensen, U., 1997. Mantle convection and stability of depleted and undepleted continental lithosphere. J. Geophys. Res. 102, 2771-2787. Doin, M.-P., Fleitout, L., McKenzie, D., 1996. Geoid anomalies and structure of continental and oceanic lithospheres. J. Geophys. Res. 101, 16119-16135. Dupeyrat, L., Sotin, C., Parmentier, E.M., 1995. Thermal and chemical convection in planetary mantles. J. Geophys. Res. 100, 497-520. Ebinger, C.J., Sleep, N.H., 1998. Cenozoic magmatism throughout East Africa resulting from impact of a single plume. Nature 395, 788-791. Gasparik, T., 1990. Phase relations in the transition zone. J. Geophys. Res. 95 (B10), 15751-15769. Gurnis, M., 1988. Large-scale mantle convection and the aggregation and dispersal of supercontinents. Nature 332, 695-699.
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Hirth, G., Kohlstedt, D.L., 1996. Water in the oceanic upper mantle: implications for rheology, melt extraction and the evolution of the lithosphere. Earth Planet. Sci. Lett. 144, 93-108. Hughes, T.J.R., Brooks, A., 1979. A multidimensional upwind scheme with no crosswind diffusion.In: Hughes, T.J.R. (Ed.), Finite Element Methods for Convection Dominated Flows, Vol. 34 of Applied Mechanics Division, American Society of Mechanical Engineers, New York. Ita, J., King, S.D., 1994. Sensitivity of convection with endothermic phase change to the form of governing equations, boundary conditions and equation of state. J. Geophys. Res. 99, 15919-15938. Jacques, A.L., Green, D.H., 1980. Anhydrous melting of peridotite at 0-15 kb pressure and genises of tholeiitic basalts. Contrb. Mineral. Petrol. 73, 287-310. Jordan, T.H., 1975. The continental tectosphere. Geophys. Space Phys. 133, 1-12. Jordan, T.H., 1979. Mineralogies, densities, and seismic velocities of garnet lherzolites and their geophysical implications. In: Boyd, F.R., H.O.A., Meyer (Eds.), The Mantle Sample: Inclusions in Kimberlites and Other Volcanics, American Geophysical Union, Washington DC, pp. 1-14. Jordan, T.H., 1988. Structure and formation of the continental tectosphere. J. Petrol., Special Lithosphere Issue, 11-37. Kameyama, M., Fujimoto, H., Ogawa, M., 1996. A thermo-chemical regime in the upper mantle in the early Earth inferred from a numerical model of magam-migration in a convecting upper mantle. Phys. Earth Planet. Inter. 94, 187-215. Karato, S., 1990. The role of hydrogen in the electrical conductivity of the upper mantle. Nature 347, 272-273. Karato, S., Jung, H., 1998. Water, partial melting and the origin of the seismic low velocity and high attenuation zone in the upper mantle. Earth Planet. Sci. Lett. 157, 193-207. Karato, S., Wu, P., 1993. Rheology of the upper mantle: a synthesis. Science 260, 771-778. Leitch, A.M., Davies, G.T., Wells, M., 1998. A plume head melting under a rifting margin. Earth and Planetary Science Lett. 161, 161-177. Lenardic, A., 1997. On the heat flow variation from archean cratons to Proterozoic mobile belts. J. Geophys. Res. 102, 709-721. Matyska, C., 1994. Topographic masses and mass heterogeneities in the upper mantle. Gravimetry and Space Techniques Applied to Geodynamics and Ocean Dynamics, Vol. 17 of Geophysical Monograph Series, American Geophysical Union, Washington, DC, pp. 125-132. McKenzie, D., 1984. The generation and compaction of partially molten rock. J. Geophys. 25, 713-765. McKenzie, D., Bickle, M., 1988. The volume and composition of melt generated by extension of the lithosphere. J. Geophys. Res. 29, 625-679. Moresi, L., Solomatov, V., 1997. Mantle convection with a brittle lithosphere: thoughts on the global tectonic styles of the Earth and Venus. Geophys. J. Int., (submitted). Mi~ller, R.D., Roest, W.R., Royer, J.Y., Gahagan, L.M., Sclater, J.G., 1996. Age of the ocean floor. Technical Report MGG-12,
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World Data Center A for Marine Geology and Geophysics, 325 Broadway, Boalder, CO 80303-3328, USA. Muyzert, E., 1996. A seismic cross section through the east European continent. Geophys. J. Int. (submitted). O'Connell, R.J., Hager, B.H., 1980. On the thermal state of the Earth. In: Dziewonski, A.M., Boschi, E. (Eds.), Phys. Earth's Int. Elsevier, New York, pp. 270-317. Ogawa, M., 1994. Effects of chemical fractionation of heat-producing elements on mantle evolution inferred from a numerical model of coupled magmatism-mantle convection system. Phys. Earth Planet. Int. 83, 101-127. Ohtani, E., Kato, T., Sawamoto, H., 1986. Melting of a model chondritic mantle to 20 GPa. Nature 322, 352-353. Polet, J., Anderson, D.L., 1995. Depth extent of cratons as inferred from tomographic studies. Geology 23 (3), 205-208. Pollack, H.N., Hurter, S.J., Johnson, J.R., 1993. Heat flow from the Earth's interior: analysis of the global data set. Rev. Geophys. 31,267-280. Ranalli, G., 1991. The microphysical approach to mantle rheology. In: Sabadini, R. et al. (Eds.), Glacial Isostasy, Sea-Level and Mantle Rheology, Kluwer, The Netherlands, pp. 343-378. Ribe, N.M., Christensen, U.R., 1994. Melt generation by plumes; a study of Hawaiin volcanism. J. Geophys. Res. 99, 669-682. Schmeling, H., Bussod, G.Y., 1996. Variable viscosity convection and partial melting in the continental asthenosphere. J. Geophys. Res. 101,5411-5423. Schott, B., Schmeling, H., 1998. Delamination and detachment of a lithospheric root. Tectonophysics (submitted). Segal, A., 1982. Aspects of numerical methods for elliptic singular perturbation problems. SIAM J. Sci. Stat. Comput. 3 (3), 327-349.
Sotin, C., Parmentier, E.M., 1989. Dynamical consequences of compositional and thermal density stratification beneath spreading centers. Geophys. Res. Lett. 16, 835-838. Sparks, D.W., Parmentier, E.M., 1993. The structure of three-dimensional convection beneath oceanic spreading centers. Geophys. J. Int. 112, 81-91. Takahashi, E., 1990. Speculations on the Archean mantle: missing link between komatiite and depleted garnet peridotite. J. Geophys. Res. 95, 15941-15954. Takahashi, E., Kushiro, I., 1983. Melting of a dry peridotite at high pressure and basalt magma genesis. Am. Miner. 68, 859-879. Turcotte, D.L., Schubert, G., 1982. Geodynamics; Applications of continuum physics to geological problems. Wiley. Van Den Berg, A.P., Van Keken, P.E., Yuen, D.A., 1993. The effects of a composite non-Newtonian and Newtonian rheology on mantle convection. Geophys. J. Int. 115, 62-78. Vlaar, N.J., Van Den Berg, A.P., 1991. Continental evolution and Archeao-sea-level. Sabadini, R. et al. (Eds.), Glacial Isostasy, Sea-Level and Mantle Rheology, Elsevier, The Netherlands, pp. 637-662. Vlaar, N.J., Van Keken, P.E., Van Den Berg, A.P., 1994. Cooling of the Earth in the Archaean; consequences of pressure-release melting in a hotter mantle. Earth Planet. Sci. Lett. 121, 1-18. Walzer, U., Hendel, R., 1997. Time-dependent thermal convection, mantle differentiation and continental-crust growth. Geophys. J. Int. 130, 303-325. Zhang, Y.-S., Tanimoto, T., 1993. High-resolution global upper mantle structure and plate tectonics. J. Geophys. Res. 98, 9793-9823.
LITHOS ELSEVIER
Lithos 48 (1999) 171-194
The age of continental roots D.G. Pearson
*
Department of Geological Sciences, Durham University, South Road, Durham, DH1 3LE, UK Received 20 March 1998; received in revised form 8 January 1999; accepted 11 January 1999
Abstract Determination of the age of the mantle part of continental roots is essential to our understanding of the evolution and stability of continents. Dating the rocks that comprise the mantle root beneath the continents has proven difficult because of their high equilibration temperatures and open-system geochemical behaviour. Much progress has been made in the last 20 years that allows us to see how continental roots have evolved in different areas. The first indication of the antiquity of continental roots beneath cratons came from the enriched Nd and Sr isotopic signatures shown by both peridotite xenoliths and inclusions in diamonds, requiring isolation of cratonic roots from the convecting mantle for billions of years. The enriched Nd and Sr isotopic signatures result from mantle metasomatic events post-dating the depletion events that led to the formation and isolation of the peridotite from convecting mantle. These signatures document a history of melt- and fluid-rock interaction within the lithospheric mantle. In some suites of cratonic rocks, such as eclogites, Nd and Pb isotopes have been able to trace probable formation ages. The R e - O s isotope system is well suited to dating lithospheric peridotites because of the compatible nature of Os and its relative immunity to post-crystallisation disturbance compared with highly incompatible element isotope systems. Os isotopic compositions of lithospheric peridotites are overwhelmingly unradiogenic and indicate long-term evolution in low R e / O s environments, probably as melt residues. Peridotite xenoliths from kimberlites can show some disturbed R e / O s systematics but analyses of representative suites show that beneath cratons the oldest Re depletion model ages are Archean and broadly similar to major crust-forming events. Some locations, such as Premier in southern Africa, and Lashaine in Tanzania, indicate more recent addition of lithospheric material to the craton, in the Proterozoic, or later. Of the cratons studies so far (Kaapvaal, Siberia, Wyoming and Tanzania), all indicate Archean formation of their lithospheric mantle roots. Few localities studied show any clear variation of age with depth of derivation, indicating that > 150 km of lithosphere may have formed relatively rapidly. In circum-cratonic areas where the crustal basement is Proterozoic in age kimberlite-derived xenoliths give Proterozoic model ages, matching the age of the overlying crust. This behaviour shows how the crust and mantle parts of continental lithospheric roots have remained coupled since formation in these areas, for billions of years, despite continental drift. Orogenic massifs show more systematic behaviour of R e - O s isotopes, where correlations between Os isotopic composition and S or Re content yield initial Os isotopic ratios that define Re depletion model ages for the massifs. Ongoing S r - N d - P b - H f - O s isotopic studies of massif peridotites and new kimberlite- and basalt-borne xenolith suites from new areas, will soon enable a global understanding of the age of continental roots and their subsequent evolution. 9 1999 Elsevier Science B.V. All rights reserved.
Keywords: Continent; Lithospheric mantle; Os isotope; Geochronology; Xenolith
* Fax: +44-191-374-2510 0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All rights reserved. PII: S 0 0 2 4 - 4 9 3 7 ( 9 9 ) 0 0 0 2 6 - 2
172
D.G. Pearson / Lithos 48 (1999) 171-194
1. W h y date lithospheric mantle?
Much of our understanding of plate tectonics and Earth processes is based on observations from crustal rocks, simply because they are the most immediately accessible but also because the context for interpreting geochemical data for the crust is much clearer. In fact, some of the first positive evidence concerning the antiquity of the continental lithospheric mantle (CLM) came from observations of isotopic diversity in erupted basalts (Brooks et al., 1976). Age constraints on the continental lithosphere address a large variety of questions such as: (i) When were the first stable continental roots formed and did these coincide with the first stable cratonic crust, i.e., does the age of the crust match that of the mantle below? (ii) How was the first CLM formed and has this process varied through time? (iii) Is the formation of crust and CLM linked? (iv) To what extent are the crust and CLM coupled during plate movement and collision? Various models for CLM growth can be envisioned, some of which are illustrated in Fig. 1. Some models might produce distinctive age structure in the CLM that may enable us to discriminate between endmembers (Fig. 1), however, if hybrid models dominate then the picture is probably very difficult to decipher. One of our tasks has been to address this question. Samples of CLM are available for study in two main forms. One is as large fragments of tectonically emplaced peridotites, known as orogenic peridotite massifs (Menzies and Dupuy, 1991b). Such massifs commonly occur at plate-boundaries. The other mode of occurrence is as small fragments of mantle entrained in volcanic rocks during eruption; mantle xenoliths (Nixon, 1987). In contrast to massifs, mantle xenoliths usually sample intra-plate lithospheric mantle and so each sample type has merits over the other, but between them they provide us with a fairly comprehensive sampling of CLM. For instance, whereas massif peridotites form samples of over 100 km 2 in some instances, allowing long-range spatial variability to be studied, xenolith suites, although much more limited in their lateral sampling, may provide fragments from the entire lithospheric depth (Fig. 2).
1 aa 0.5 Ga
~
a~ ~ o-"~_~ ~o
2.4 Ga
._._~ 0.5 Ga
o.5 aa~"~...~...3.~o.5 aa Lateral "block" accretion g~43 0~2 ~
2
Fig. 1. Hypothetical models of continental root formation with possible age relationships. Hybrids between the different endmember models can also be envisaged.
The array of calculated equilibration pressures and temperatures illustrated in Fig. 2 suggest that some lithospheric xenoliths are derived from depths of at least 200 km. In fact, such plots provide a first order view of the potential antiquity of cratonic lithosphere in that the P/T arrays for xenoliths from both Cretaceous and Proterozoic kimberlites (Premier) indicate no change in lithospheric thickness over this time period.
D.G. Pearson/Lithos 48 (1999) 171-194
A
P GPa
173
least the upper portions of the continental crust. Neither of these two criteria are likely to be satisfied in rocks originating from the lithospheric mantle and it is unlikely that the geochronology of the continental (or oceanic) lithospheric mantle will ever be as well constrained and precisely known as that of the overlying crust. This is largely due to one major factor readily evident in Fig. 2: temperature. The high ambient temperature of most of the CLM, under even cool cratonic geothermal conditions, is probably above the blocking temperature of most isotopic systems in most minerals that could be used for multi-mineral or rock isochron-type dating. In addition, these high temperatures promote reaction between mantle and infiltrating fluids such that disturbance of isotopic systems is readily achieved. Also, the scarcity of phases such as zircon in the mantle limits the application of U - P b techniques in accessory phases, which has done so much to resolve problems in crustal geochronology. Despite these problems, some remarkable progress has been made.
-
-
lib
2. Isotopic signatures of C L M
Fig. 2. P~ T plot showing equilibration conditions of southern
African xenoliths compared to the likely blocking temperatures for commonly used isotopic systems. Data from Danchin (1979), Finnerty and Boyd (1987), and Boyd (unpublished). The "kink" in the P / T arrays shown here is not present if some other thermobarometer combinations are employed. See Dickin (1995), and Heaman and Parrish (1991) for blocking temperature estimates.
One of the problems of obtaining age information on samples of CLM using radiogenic isotope systems has been the very low levels of the elements of interest, and so application of these techniques did not really proliferate until the development of modem mass spectrometers in the late 1970s. To understand the genesis and evolution of continental roots it is desirable to have similar stratigraphic and geochronological constraints to those available for at
It is not within the scope of this work to review the basics of the radiogenic isotope systems commonly used in the study of CLM and readers are referred to relevant texts, e.g., Faure (1986) and Dickin (1995). The contribution of S r - N d - P b isotope systems to the characterisation and origin of CLM has been thoroughly reviewed by Menzies (1990). It is worth noting some features of the Re-Os system before proceeding. The advantages of the Re-Os isotope system for obtaining age information were emphasised by Walker et al. (1989a) and Shirey and Walker (1998). The main attractions to this system are discussed below. (i) Os is abundant in mantle rocks relative to either their host magmas, in the case of xenoliths, or most post-crystallisation metasomatic fluids/melts, in the case of both xenoliths and orogenic massifs (Fig. 3), such that it is more robust to disturbance than isotope systems based on incompatible elements (elements concentrated in the liquid phase during partial melting). (ii) Minimum ages of separation of peridotites from the convecting upper mantle can still be ob-
174
D.G. Pearson/Lithos 48 (1999) 171-194
Fig. 3. Illustration of the effects of simple mixing of a peridotite xenolith and host kimberlite magma on the Os isotope composition of the bulk rock xenolith and the Nd isotope composition of diopside from the xenolith (the bulk rock is usually measured for Os isotopes and a diopside or garnet separately measured for the Nd isotope composition). The effects of older interaction, at 1.1 Ga, followed by time-integrated in-growth of radiogenic Os from introduced Re is also modelled. Os isotopic compositions lying to the left of the dashed line give Archaean TRD ages. It is noteworthy that large amounts of kimberlite interaction are required to destroy the signature of Arcaean depletion in a peridotite. See Fig. 13 caption for definition of TRo age.
")/Os(t)= [ (1870S/ 188OSsample(t))/ (1870S/1 880Schondrite(,))] ENd(t ) =
x 100. [ (143Nd/144Ndsample(t))/(143Nd/144 Ndchondrite(t))] • 10000.
tained, even if parent-daughter ratios have been disturbed (see below). (iii) Mantle melting produces marked fractionations of Re from Os that rapidly evolve into distinct time-integrated isotopic signatures for both melts and reservoirs. Because of these features, the Re-Os isotope system has proven particularly successful in the study of CLM. One of the objectives of this contribution is to evaluate more thoroughly the robustness of some aspects of the system.
2.1. CLM isotopic heterogeneity Once the overprint of host-magma and low-T alteration on mantle derived rocks has been properly
accounted for (see detailed leaching studies on minerals by Richardson et al. (1985), Jagoutz (1988), and Pearson et al. (1993), and review by Pearson (in press), one of the most striking features of the isotope database for CLM is its heterogeneity. Samples from both on- and off-craton settings display much greater Nd-Sr isotope variation than the oceanic mantle (Fig. 4). This heterogeneity must result from the long-term isolation of CLM from the homogenising effects of convective stirring and diffusion at the higher temperatures prevailing in convecting mantle. Heterogeneity is also evident for Pb isotopes (Menzies, 1990)) and Os isotopes (Fig. 5). Two other features are evident from these compilations of data. Firstly, although the commonly proposed origin for most CLM involves initial melt depletion (i.e., they are melting residues), in Sr-Nd isotope space, a great many samples plot in the enriched quadrant of the isotope plot. This contrasts with Os where samples predominantly have negative YOs, characteristic of an ancient, residual character. Secondly, to uniquely define CLM in Nd-Sr isotope space (or in isotope space involving Pb isotopes) is very difficult, whereas the Os isotopic composition of CLM appears to be clearly distinct from oceanic mantle, with continental crust being grossly displaced to more radiogenic values than those plotted on Fig. 5. Hence, Os appears to be a powerful tool for identifying ancient CLM and this property is being utilised in tectonically complex areas where the likely nature of the lithospheric root is unclear (e.g., Handler et al., 1997; Hassler and Shimizu, 1998). Recent analytical advances will now permit Hf isotopic characterisation of the CLM and use of potentially useful combined Hf-Os isotopes (McDonough, 1994). An idea of the length scale of isotopic variation in the CLM is probably best obtained from orogenic peridotites. Considering only the peridotites, isotopic variations that are large fractions of the total variability of oceanic mantle are present over km scale distances (Reisberg and Zindler, 1986; Zindler and Hart, 1986). When the pyroxenites are considered, isotopic variations in Nd and Pb occur over 10s of cm in most massifs that are considerably greater than those shown by oceanic mantle, (Reisberg and Zindler, 1986; Reisberg et al., 1989; Downes et al., 1991; Mukasa et al., 1991; Reisberg et al., 1991; Pearson et al., 1993; Kumar et al., 1996). Although
D.G. Pearson / Lithos 48 (1999) 171-194
175
t-
Fig. 4. Sr-Nd isotope compositions of diopsides or garnets (where garnet is the only Ca-Al-rich phase) for lithospheric peridotites compared to oceanic mantle (inset) and continental crust. Cratonic mantle peridotites solid symbols, non-cratonic peridotites open symbols. Peridotite data from references listed in Menzies (1990) plus Carlson and Irving (1994), Gunther and Jagoutz (1994, 1997), Pearson et al. (1995a,c).
not quantifiable in terms of length scale, an idea of the local CLM isotopic variability sampled by individual kimberlites bearing xenoliths, is illustrated by the 42 end unit variation in initial Nd isotope composition shown by individual garnet crystals from the Udachnaya kimberlite pipe (Jacob et al., 1998). The garnets analysed by Jacob et al. (1998) and similar garnets analysed by Pearson et al. (1995c) vary from + ve initial ~ONd values to strongly negative (to ~~ --55) and indicate the potentially complex behaviour of incompatible element-based isotope systems in CLM samples. On a single rock scale, Jagoutz (1988) found 16 ~~ units variation within different magnetic fractions of garnet from the same Tanzanian eclogite xenolith. This type of variation indicates that if melt
fractions are removed in different batches from even a single CLM sample, they have the potential to create magmas with widely varying isotopic compositions from the same source rock. Probably the largest magnitude of isotopic variability in the CLM comes from the pyroxenites and eclogites that are interspersed throughout it and sampled as xenoliths by kimberlites and other deeply derived magmas. This variability is by far the most pronounced for Os isotopes (Fig. 6), the total variation within single suites of eclogites and pyroxenites being much greater than oceanic mantle, indicating the potentially dramatic effect of incorporating such components into magmas during mantle melting. Although different isotopic systems may reflect the effects of enrichment, or depletion, the extreme
176
D.G. Pearson/Lithos 48 (1999) 171-194
nature of the isotopic variations observed is a clear indication of the general antiquity of the CLM reservoir. The quantification of how old these isotopic signatures might be is outlined below. 10
[i:...:..:t
E
Kaapvaal peridotites
6
~ "i "" " ""
4
Z
4
-
Siberian peridotites
D Low-T r:(1 H ig h -T
0
d z
2
0
f Wyoming peridotites
3 E ~o d
2
Z
1
0 6
Oceanic mantle peridotites E
4
~
E
0
Z
~
2
[! D []
3. Age constraints 3.1. Mineral and whole rock isochrons
Consideration of published diffusion coefficients e.g., Sneeringer et al. (1984), together with likely length scales of diffusion for two minerals such as diopside and garnet in a coarse grained garnet peridotite show that at lithospheric temperatures, above 1000~ diffusion will out-pace radiogenic ingrowth of daughter isotopes in most circumstances. Hence, the application of the isochron technique to examine lithospheric age will be somewhat limited (Zindler and Jagoutz, 1988). Given the effort involved in analysis, this method has yielded relatively little clear information on the chronology of lithospheric processes. For example, analysis of orthopyroxene, clinopyroxene and garnet from a low-temperature peridotite from the Premier kimberlite (Fig. 7) yielded an isochron age that is within error of the Proterozoic emplacement age of this kimberlite (Pearson et al., 1995a). Other studies that have obtained mineral isochrons defining the approximate age of kimberlite eruption include garnet lherzolites (Richardson et al., 1985; Walker et al., 1989a; Pearson et al., 1995c) and eclogites (Snyder et al., 1993; Pearson et al., 1995c). Minerals in xenoliths erupted by much younger, alkali-basalt magmas are often in, or close to, Nd isotopic equilibrium (Jagoutz et al., 1980; McDonough and McCulloch, 1987). More obvious success has been achieved where mineral isochrons have successfully been used to estimate the age of emplacement of orogenic peridotite massifs. This approach relies on garnet and pyroxene cooling past the Sm-Nd blocking temperature on emplacement of the peridotite bodies into the crust. The large difference in S m / N d fractionation between garnet and pyroxene means that even relatively young emplacement ages can be fairly precisely constrained by mineral isochrons from garnet
Ophiolites Abyssal OIB xenoliths
L
-10
Fig. 5. Histograms of Os isotopic compositions of cratonic peridotite xenoliths expressed as initial Yos values (at the time of kimberlite eruption; see Fig. 3 for calculation) compared to oceanic mantle. Data sources: Walker et al. (1989a), Luck and Allbgre (1991), Hauri et al. (1993), Carlson and Irving (1994), Snow and Reisberg (1995), Pearson et al. (1995a,c), and Pearson, unpublished.
D.G. Pearson/Lithos 48 (1999) 171-194
.~_,.~_,.~_,.~_o~'.~_,~;~_;~_;~_;~_~'._ 9
177
;_ "._ "._ ;_ ;_ ;~_'._ ;_ ;_ "._ "._ ;~_'._ ;_ "._ ;_ ;_ ;_ "._ IN_
Fig. 6. Os isotope variation (as Yo~) in various lithologies from continental roots compared to crustal rocks (data sources as in Fig. 5 plus Walker et al. (1989b), Reisberg et al. (1991), Esser and Turekian (1993), Reisberg and Lorand (1995), Pearson et al. (1995d), Burnham et al. (1998), Menzies et al. (1998), Shirey et al. (1998)).
lherzolites and garnet pyroxenites and this method has been successfully employed in this way for both Ronda and Beni Bousera peridotite massifs (Zindler et al., 1983; Reisberg et al., 1989; Pearson et al., 1995b). More ancient mineral isochrons, significantly in excess of eruption ages, have been determined for diopside-garnet pairs in cratonic peridotites (Walker et al., 1989a; Pearson et al., 1995a,c; Gunther and
]44 Fig. 7. S m - N d mineral isochron for a low-temperature garnet lherzolite from the Premier kimberlite, S. Africa. Data from Pearson et al. (1995a). Error bars are smaller than symbols, error on age is 2 sigma.
Jagoutz, 1997) and eclogites (Jagoutz, 1988; Jagoutz et al., 1984; Jacob et al., 1994). Garnet-diopside mineral isochrons from a single kimberlite pipe can vary widely in slope, giving apparent ages that are hundreds of Ma different (Fig. 8). The geochronological information provided by these isochrons is unclear. Wide variations in isochron ages from similar xenoliths in a single kimberlite are unlikely to simply represent closure ages due to post-formation cooling (Pearson et al., 1995c). In addition, even if mineral dis-equilibria was a simple function of cooling, the complex relationship between diffusion and in situ radiogenic growth (Zindler and Jagoutz, 1988) means that a given isochron "age" cannot readily be linked to any specific event. Contamination by the host kimberlite can alter peridotite mineral isochrons, complicating the situation further (Gunther and Jagoutz, 1997), but this can usually be readily identified. Gunther and Jagoutz (1997) propose that the oldest mineral isochrons in Siberian peridotites, of ca. 2 Ga, represent closure ages. Younger ages represent partial closure/re-equilibration during either lithospheric residence or during eruption. In situ trace element measurements of minerals from some of these rocks provide a different perspective. The frequent presence of both fine-scale (100 IxM) zonation, and non-equilibrium partitioning
178
D.G. Pearson/Lithos 48 (1999) 171-194
peridotite
~
o.52o
0.5
Fig. 8. Garnet-diopside Sm-Nd mineral isochrons for peridotites from the Mir kimberlite pipe, Siberia (McCulloch, 1989; Zhuravlev et al., 1991" Pearson et al., 1995c; Gunther and Jagoutz, 1997).
behaviour for REE between many garnets and clinopyroxenes from Siberian peridotites (Shimizu et al., 1997a) suggests disruption of isotope systematics in many peridotite minerals due to recent mineral growth. In addition, REE inter-mineral element partitioning indicates non-equilibrium between minerals in numerous instances (Shimizu et al., 1997a). These complexities make interpretation of the slope of mineral isochrons for lithospheric peridotites a subjective matter, and detailed studies of mineral zonation are required for more secure interpretation. Despite this, some xenoliths appear to give plausible mineral isochron ages such as the 1.75 _+ 0.01 Ga Sm-Nd isochron age for multiple garnet and clinopyroxene fractions from an eclogite xenolith (Jagoutz, 1988), interpreted to reflect the time of major mineral equilibration during emplacement into the lithosphere. This isochron age can be related to a regional thermal event in the Tanzanian crust. The high initial end value of 25 for the isochron implies that the source/protolith for the eclogite could be much older. It is possible that the Tanzanian eclogite studied by Jagoutz (1988) could be of crustal origin (Rudnick et al., 1998, personal communication) and that the 1.75 Ga isochron age could therefore repre-
sent a thermal effect in the crust that would have presumably manifested itself in the mantle in some way. Perhaps a more successful approach to S m / N d isochrons is to increase the diffusion length-scale by analysing minerals, e.g., diopsides, from different xenoliths that may have been separated by considerable distances in the mantle. An example of this approach is given by Deng and McDougall (1992) who analysed diopsides from a suite of spinel peridotites from Inner Mongolia. These authors obtained a good correlation on a Sm-Nd isochron diagram that yields an age of 1.64 _+ 0.01 Ga (Fig. 9). This age is taken to represent the time of their differentiation from the convecting mantle. Regional enrichment events in the mantle lithosphere can also be constrained using this approach (e.g., Carlson and Irving, 1994). Isochronous relationships have been obtained on some eclogite suites using the Re-Os system. A diamondiferous eclogite suite from Udachnaya, Siberia yields a whole rock Re-Os isochron of 2.94 _+ 0.38 Ga (Pearson et al., 1995d), whereas a diamondiferous suite from the Newlands kimberlite, S. Africa (Menzies et al., 1998) gives a whole rock
D.G. Pearson/Lithos 48 (1999) 171-194
179
spinel I
Fig. 9. Sm-Nd isochron and model ages for diopside separates from Mongolian peridotites analysed by Deng and McDougall (1992).
isochron age of 3.5 _+ 0.7 Ga. In these examples, the Os and possibly Re, reside in dispersed sulfide grains throughout the xenoliths. It appears that, at least for the Udachnaya and Newlands suite, for the length scale sampled by individual xenoliths, the Re-Os system has been effectively isolated from diffusional equilibration and has been immune enough to hostrock interaction (in contrast to Sm-Nd isotopes, e.g., Snyder et al., 1993) to preserve useful age information. The validity of the Udachnaya Re-Os isochron is supported by model age information in the case of the Udachnaya suite (see below).
3.2. U-Pb accessory phase dating Kimberlites contain a variety of accessory phases, including zircon, perovskite and baddelyite, that commonly yield U-Pb ages equivalent to the age of pipe emplacement (Davis, 1978; Heaman, 1989; Kinny et al., 1997; Scharer et al., 1997). Zircons are relatively common in highly metasomatised xeno-
liths such as MARID's and their ages can be related in some instances to enrichment events that preceded kimberlite eruption, probably earlier in the Cretaceous (Hamilton et al., 1998; Konzett et al., 1998). Some megacrystal zircons have yielded indications of very ancient derivation, in the Archaean (Kinny et al., 1989), but as they are discrete crystals it is difficult to relate this information geologically, other than to a likely lithospheric enrichment event. Better constrained information on lithospheric chronology comes from the rare crystals of zircon and monazite found within peridotite xenoliths themselves. Both these phases must be products of lithospheric enrichment and as such they relate to lithospheric modification rather than reflecting processes involved in the initial stabilisation of CLM. Nonetheless, the opportunity exists to obtain very precise estimates of enrichment ages and hence precise estimates of minimum lithosphere ages. Carlson and Irving (1994) report data from a monazite extracted from a glimmerite nodule from Montana that gives a precise
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D.G. Pearson / Lithos 48 (1999) 171-194
232Th/2~ age of 1806_+ 1 Ma. Minerals and wholerocks from the same suite scatter about a 1.8 Ga S m / N d isochron indicating that this event affected most of the lithosphere sampled, but the monazite provides a much more precise date for the enrichment. The same enrichment age has recently been confirmed by U - P b analyses of zircons (Rudnick et al., in press) from a glimmerite xenolith similar to that analysed by Carlson and Irving (1994), the average of the z i r c o n 238u/Z~ ages being 1798 + 18 Ma, but with some indication of Pb loss. In contrast to ancient mantle zircons from Montana, those extracted from a Tanzanian harzburgite (Rudnick et al., in press) are extremely young, with a m e a n 238u/Z~ age of 400 _+ 200 Ka. Thus, some of these phases must have crystallised during events closely preceding eruption (Kinny and Meyer, 1994; Rudnick et al., in press). The ancient ages recorded by monazites and zircons within both xenoliths and as megacrysts raise interesting questions about our knowledge of U - P b blocking temperatures in zircons, generally held to be ca. 800~ (Heaman and Parrish, 1991). Some of the Montana xenoliths may have very low equilibration temperatures, possibly being derived from the lower crust. However, as pointed out by Kinny et al. (1989) zircon megacrysts probably crystallise at much higher temperatures, and spend most of their existence at temperatures well above 800~ bringing into question current estimates of the blocking temperature. A > 800~ blocking temperature for U - P b diffusion in zircon is further supported by the 628 +_ age obtained for a zircon inclu12 M a 238u/Z~ sion in a diamond erupted by the Cretaceous Mbuji-Mayi kimberlite (Kinny and Meyer, 1994). If this diamond and its inclusion crystallised in the typical "diamond window" then a formation temperature above 900~ is likely. 3.3. The model age approach Because of the high ambient temperature of lithospheric mantle, and the scarcity of high U - T h accessory phases amenable to U - T h - P b dating, the most commonly used method of constraining the age of CLM is the model age approach. This technique requires a number of assumptions to be valid. One is that the rock remains a closed system since the event being dated, and another is that we have adequate
prior knowledge of the reservoir from which the rock differentiated. Because these assumptions are not always valid for the rocks being studied, model ages for mantle samples must be carefully scrutinised. For xenolith suites, the susceptibility of incompatible element-based isotope systems to disturbance by either host magma, or pre-eruption metasomatic agents, likely to have infiltrated the lithosphere over time (McKenzie, 1989), Fig. 3, means that few sample suites are likely to give consistent results. The latter process also disrupts Nd isotope systematics in orogenic peridotites (Reisberg and Zindler, 1986), with the additional complication of the likelihood of melting during ascent and emplacement into the crust that may decouple parent-daughter ratios (Pearson et al., 1993). 3.3.1. Nd isotope model ages One xenolith suite which appears to record consistent Nd-model age systematics is the Mongolian peridotite suite studied by Deng and McDougall (1992). CHUR Nd-model ages for diopsides from most of these xenoliths range from 1.1 to 1.7 Ga and cluster close to the 1.6 Ga mineral isochron (Fig. 9). Published diopside Nd isotope data from Bultfontein xenoliths also yield consistent model age results, with most samples having depleted mantle Nd model ages of ca. 1.1 Ga (Fig. 10). Although some of these samples contain garnet, isotopic evidence indicates that this phase has not equilibrated with the diopside (Gunther and Jagoutz, 1994) and contributes little to the bulk-rock Nd budget. Hence, Nd isotopes of the diopsides are a reasonable approximation of the bulk-rock Nd isotope evolution. Selection of Bulk Earth as the parent reservoir for the Bultfontein xenoliths (Fig. 10) results in more complex Nd isotope evolutionary histories, with greater variation in model ages and an overall decrease in age. The ages produced from this approach would be enrichment ages in the sense that their Nd evolution lines diverge from that of Bulk Earth at shallower angles, indicating evolution with S m / N d < Bulk Earth. This plot clearly illustrates the fundamental difficulty in deciding which parent reservoir is most appropriate for the model age calculation and the complications that this can induce. All CLM samples will be potentially subject to post-crystallisation metasomatism. Richardson et al.
181
D.G. Pearson/Lithos 48 (1999) 171-194
Z
Z 0.5115 0.5110 0.0
2.0
T Ga Fig. 10. Nd model ages of diopsides from Bultfontein peridotite xenoliths. Data from Richardson et al. (1985) and Gunther and Jagoutz (1994). Dashed line highlights the most aberrant sample. Although these samples contain garnet, it is usually not very radiogenic and in many cases it is unequilibrated with the diopside (Gunther and Jagoutz, 1994). The Nd budget of the rock is largely reflected by diopside in this case.
(1984) used the non-reactive, armouring properties of diamond to advantage in analysing syngenetic garnet inclusions within diamonds, with the aim of constraining the time of garnet, and hence diamond crystallisation. The garnets first analysed were of
sub-calcic composition, belonging to the harzburgitic paragenesis. Compositing of many different garnet inclusions from numerous different diamonds from the Finsch and Kimberley mines gave Nd model ages of over 3 Ga (Fig. 11). The very low eNa values of these garnet composites indicate diamond formation in ancient, enriched CLM. Analysis of two other sub-calcic garnet inclusion composites from the Premier mine (Richardson et al., 1993) produced a Bulk Earth model age older than the Earth for one sample. This result was attributed to the similar S m / N d value of the sample and reference reservoir, which combine to produce potentially large errors in estimated model ages. This potential imprecision must be borne in mind when dealing with model ages. Rigorous treatment of error propagation for model age calculations is presented by Sambridge and Lambert (1997). The ancient ages of sub-calcic garnet inclusions in diamonds (Richardson et al., 1984) is commonly quoted as some of our most reliable evidence for the antiquity of CLM, based on the premise that the diamonds have protected the garnets from subsequent interaction with mantle fluids since their encapsulation. Recently, alternative explanations have been offered for the Sm-Nd and Rb-Sr isotope systematics
r
0.0
1.0
2.0
3.0
4.0
T Ga Fig. 11. Nd model ages for sub-calcic garnet inclusions in S. African diamonds (Richardson et al., 1984, 1993).
182
D.G. Pearson/Lithos 48 (1999) 171-194
of the sub-calcic garnet inclusions in diamonds analysed by Richardson et al. (1984); firstly, on the basis of the complexity of Sr isotope systematics of the garnets, that require an unusual pre-history (Pidgeon, 1989; Pearson et al., 1995c) and, secondly, on the basis of observed elemental zonation in numerous garnet inclusions in diamonds of this type (Shimizu and Sobolev, 1995; Shimizu et al., 1997b). A notable finding in this regard is that the concept that diamond is always a robust shield against postcrystallisation metasomatism is doubtful from the observation of healed fractures, observable only in cathodoluminescence, in some diamonds (Taylor et al., 1995). 3.3.2. Whole rock xenolith Os isotope model ages and system robustness Simple mixing calculations (Fig. 3) show that Os isotopic compositions are much less prone to metasomatic disturbance compared with Nd. If hostkimberlite contamination of a peridotite xenolith is considered, large mass fractions, considerably in excess of 10%, are required to obscure direct isotopic evidence of an Archaean origin (Fig. 3). Older metasomatism can be more effective in altering time-integrated Os isotope compositions due to the appreciable Re contents of most mantle melts (Fig. 3). The relatively high Re contents of mantle melts compared to peridotites means that peridotite R e / O s values are likely to reflect some component of metasomatic enrichment. This is true for both xenolith and orogenic peridotite samples. Some xenolith suites from alkali basalts show coherent Re-Os systematics that largely reflect melt depletion (Handler et al., 1997) but cratonic xenolith suites appear to be thoroughly disrupted. It is not presently clear how much of the overall disruption of R e / O s is related to mantle metasomatism and how much is due to sulfide breakdown and alteration (Lorand, 1990), but the various cratonic peridotite xenoliths that have bulk Re contents and R e / O s higher than Bulk Earth (Walker et al., 1989a; Pearson et al., 1995a) have either experienced Re addition (Fig. 12) or some early Re analyses were subject to large variable blank corrections. New data for peridotite xenoliths from the Kaapvaal craton (Carlson et al., in press) show higher percentages of xenoliths with very low Re contents, as low as 5 ppt. In contrast, more
obviously metasomatised peridotite xenoliths from the margin of the Tanzanian craton have a larger range in R e / O s with Re contents reaching over 300 ppt (Chesley et al., in press). Xenolith samples with low 187Os/188Os yet elevated Re in Fig. 12 could have experienced recent Re addition, either by the host kimberlite, or possibly carbonatite-like fluids. In addition to Re enrichment, addition of high-Os fluids may also perturb Os isotope systematics in lithospheric samples (Chesley and Rudnick, 1996). This observation is supported by the presence of abundant sulfides within deformed Tanzanian peridotites that show complex Re-Os systematics (Chesley et al., 1998). Furthermore, the observation of young diamond inclusion sulfides containing very high Os (5000 to 20,000 ppb) and Re (700 to > 2000 ppb) (Pearson et al., 1998a) illustrates the potential of sulfides crystallising from metasomatic fluids for disrupting Os isotope systematics (Fig. 12). Because of complexities due to metasomatic disturbance of various types, two model age approaches are usually adopted for the Re-Os isotope system when constraining ages in lithospheric peridotites. A "normal" model age approach (TMA ages)utilises the measured Os isotope composition and R e / O s of the sample and assumes closed system behaviour (Fig. 13). In cases where disruption of R e / O s is suspected, as in many cratonic peridotite xenoliths, the Re depletion or TRD model age is generally used. The TRD age assumes that all Re is consumed during formation of the peridotite and hence the calculation is made using a R e / O s of zero. In cases where the degree of melting is relatively low and Re is not exhausted, TMA will exceed TRD, i.e., TRD will be an underestimate of the real age (Fig. 13). In cases where the degree of melting is large, e.g., 30% or more, leading to Re exhaustion, then TMA will equal TRI~ (Fig. 13). The equations and parameters for these calculations are given in Fig. 13 and are discussed at length by Walker et al. (1989a), Pearson et al. (1995a), and Shirey and Walker (1998). The TRD age effectively gives a minimum estimate of the sample age. Any residual Re present in the sample since formation, or added by metasomatism, will decrease the calculated age of the sample. Because many kimberlite-borne xenoliths experience infiltration by their hosts, the TRD age calculation can be modified to account for post-eruption in-
D.G. Pearson / Lithos 48 (1999) 171-194
9
,,"
183
o~'" o
,"
0 o
Fig. 12. Plot of 1870S/1880S VS. ]87Re/]88Os for (A) cratonic peridotites illustrating possible field for interaction with: the host kimberlite (shaded; Pearson et al., 1995c), high Re-Os sulfides (from Pearson et al., 1998a,b), and carbonatite (Pearson et al., 1995c); (B) Pyrenean peridotites (Reisberg and Lorand, 1995). Area labelled BE is the range of values estimated for Bulk Earth by Walker et al. (1989a,b), Meisel et al. (1996), and Luck and Allbgre (1991).
growth of radiogenic Os by calculating TRD from the xenolith initial Os isotope ratio at the time of eruption (Pearson et al., 1995a). For relatively young xenoliths, unless severely metasomatised, this makes little difference to the age calculation, but for xenoliths erupted by much older magmatism, e.g., the 1.1 Ga Premier kimberlite, this correction is considerable (Fig. 13).
Some alkali basalt-borne xenolith suites, particularly those dominated by anhydrous lithologies, have relatively undisturbed R e / O s systematics, where TMA approximates to TRD within 100 Ma in some cases, e.g., Handler et al. (1997). For kimberlite-derived xenoliths, the degree of disturbance is much more variable and TMA may be considerably greater than TRD, and can often be greater than the age of the
D.G. Pearson / Lithos 48 (1999) 171-194
184
I
TRD
I
Residue 30% melting TMA = TRD ~ ,~,,~/. . . .
" ' ' .
~TRD
~~TRDerup.
1
Fig. 13. Illustration of the TMA and TRD model age approach to peridotites. TRD = 1/A * In i.Itk187Os/188OSBE(t) -- 1870S/1 88OSsample(t ))//(187Re/188OSBEt))+l] ( TMA = 1/A * In [ (187Os/188OSBE(t) -- 1870S/188 OSsample(t ) )/(187Re/188 OSBE(t) -- 187Re/188 Os sample(t)) + 1 ] where subscripts are: BE is the Bulk Earth reservoir, usually taken as chondrite; t is the time of eruption. Following Shirey and Walker (1998), parameters are: AI87Re-- 1.666.10 -11 year -l" 1870S/1880SBE at a given time is calculated from the most primitive initial 187Os/188Os for early solar system materials (IIIA irons; 0.09531) and the average lS7Re/18SOs for chondrites of 0.40186. TRD Erup shows the effect of subtracting post-emplacement radiogenic Os ingrowth of 187Os from xenoliths erupted by ancient kimberlite pipes (e.g., Premier) on the normal TRD model age. For young kimberlites the difference between TRD and TRD Erup is insignificant unless the xenolith has very high Re/Os. Inset shows hypothetical effects of various degrees of melt extraction on the Os isotope evolution of a residual peridotite.
Earth (Fig. 14). Some xenolith samples plot close to the 1" 1 TRa/TMA line on Fig. 14, in particular, the
I
..._
2.5
0.0
Fig. 14. TMA VS. TRD plot of Os model ages for kimberlite-derived xenoliths from S. Africa (Walker et al., 1989a; Pearson et al., 1995a), Siberia (Pearson et al., 1995c) and Namibia (Pearson et al., 1994). The TMA scale is truncated at 10 Ga but extends much higher.
cluster of samples close to 2 Ga, composed of samples from Namibia and the Premier kimberlite in S. Africa (see below). However, in general most cratonic samples show evidence of disturbance with TMA > TRD. In this situation, numerous samples from a given locality/region are analysed and the oldest TRO ages are taken to approximate to the age of initial lithosphere stabilisation. The spread of ages is generally interpreted to indicate later, metasomatic disturbance. One final caveat to be mindful of when interpreting Os model ages in general is that our knowledge of the present-day Bulk Earth Os isotope composition is relatively unconstrained, with estimates varying from lS7Os/lSSOs of 0.129 or higher (Martin, 1991; Meisel et al., 1996) to average carbonaceous chondrite values of ~ 0.127 (Walker and Morgan, 1989) or even lower (Luck and All~gre, 1991). In the case of cratonic xenoliths, where ages are generally quite ancient (2 Ga or more), this problem is minimised slightly due to the precisely constrained type
D.G. Pearson/Lithos 48 (1999) 171-194
IIIA iron meteorite initial Os isotope composition (Smoliar et al., 1996). However, this uncertainty remains probably the major error factor in Re-Os model ages. For example, where using a ~87Os/lgSos of 0.129 (Meisel et al., 1996) compared to average carbonaceous chondrites ( ~ 0 . 1 2 7 ) can result in model age differences of up to 300 Ma. The variability of modern day oceanic mantle has not yet been fully defined. Recently, Parkinson et al. (1998) have recorded unradiogenic 187Os/188Os as low as 0.1193 in xenoliths believed to have been derived from the oceanic mantle wedge beneath the Izu-Bonin-Mariana forearc. These peridotites give 1.2 Ga Re depletion ages using chondritic mantle Os evolution parameters. The observation of such unradiogenic Os in fragments of probably convecting oceanic mantle raises the possibility that modern oceanic mantle contains poorly mixed portions of material that has experienced older depletion events, or that the Os isotope evolution of the upper mantle has not been homogenous. Parkinson et al. (1998) suggest that subduction zones may be graveyards for ancient depleted mantle material. It remains to be seen how wide-spread this phenomena is. The implication is that if such Os isotope heterogeneity is a widespread feature of the mantle, then Re depletion model ages in peridotites must be interpreted with even more caution. However, if these environments are restricted, it might be that most lithospheric mantle generated in Archean and Proterozoic environments did not sample such heterogeneous domains, especially if plume-dominated melting is invoked for generation of ancient CLM (Herzberg, 1992; Pearson et al., 1995a). More accurately assessing the Os isotopic evolution of the Earth's mantle remains a major goal in furthering the use of Os isotopes in mantle studies. 3.3.3. Mineral Re-Os isotope model ages It is possible to try to minimise the effects of post-crystallisation R e / O s fractionation by analysing phases with very high Os and very low Re/Os, or phases capable of armouring hosts for Re and Os from later, post-magmatic interaction. Analysis of chromite from peridotite xenoliths has shown this phase to sometimes contain very high Os, but low Re contents, making it useful in estimating the initial Os isotopic composition of systems where the bulk rock
185
may have suffered substantial new Os or Re addition, reducing TRD model ages (Chesley and Rudnick, 1996; Nagler et al., 1997). It is not understood whether the high Os contents of chromites are due to micro-inclusions of sulfides, e.g., Thalhammer et al. (1990), or whether this reflects preferential partitioning of Os into the spinel structure (Capobianco and Drake, 1990). The experiments bearing on this problem have been performed in the absence of sulfide and the observation of variable Os contents in chromites point to inclusions as the dominant control. If sulfide inclusions or PGE alloys are the main cause of high Os contents within chromites, once enclosed, the chromite "armour" will be effective in protecting the sulfide grains against further interaction with metasomatic agents. Although this method may be effective in some instances, its application may be limited by the scarcity of suitable chromites. Not all chromites may contain high Os inclusions, and low-Cr spinels in xenoliths frequently contain very little ( < 1 ppb) Os (Pearson et al., 1998b). In addition, metasomatic rims are sometimes present on chromite grains which require abrading prior to dissolution (Chesley and Rudnick, 1996). For example, Chesley and Rudnick (1996) and Chesley et al. (1998) find primary, high Cr-spinels from peridotite xenoliths from Labait, Tanzania with TRD ages of 2.7-2.9 Ga., whereas secondary, Cr-rich spinels have much lower TRD ages of 2 Ga. 3.3.3.1. Regional xenolith Re-Os studies. Regions where well characterised suites of xenoliths have been analysed for Re-Os isotopic compositions, to study lithospheric evolution, include the Kaapvaal craton (Walker et al., 1989a; Pearson et al., 1995a), the Wyoming craton (Carlson and Irving, 1994), the Siberian craton (Pearson et al., 1995c), the Tanzanian craton (Chesley et al., 1998), Namibia (Pearson et al., 1994), SE Australia (Handler et al., 1997), the Eifel region (Cohen et al., 1996) and the Vitim region of southern Siberia (Pearson et al., 1998b). If histograms are plotted for TRD ages of the three cratonic peridotite data sets published so far, we see that the oldest TRD ages are between 3 and 3.5 Ga, with the Kaapvaal frequency distribution showing pronounced peaks for late- to middle-Archaean ages (Fig. 15). The oldest TRD ages for Tanzanian peridotites are from chromite separates with TRD ages as
186
D.G. Pearson/Lithos 48 (1999) 171-194
I Kaapvaal peridotites
i
]
I
1
[ Wyoming peridotites ]
Siberian peridotites
m Fig. 15. Histograms of TRD ages for peridotite xenoliths from the Kaapvaal (Walker et al., 1989a; Pearson et al., 1995a), Wyoming (Carlson and Irving, 1994), and Siberian (Pearson et al., 1995c) cratons, ages in Ga. Bushveld and Witwatersrand ages taken from Hart and Kinloch (1990). Ancient gneiss complex data are Sm-Nd ages from Carlson et al. (1983).
old as 2.9 Ga (Chesley et al., 1998, Chesley et al., in press). While bearing in mind that these ages could be minima, some striking observations can be made. For the Kaapvaal suite, the oldest TRD ages broadly match the age of the major crust building period and also are equivalent to the oldest Os ages obtained from detrital osmiridiums from the Witwatersrand basin (Hart and Kinloch, 1990) which reflect mantle extraction ages. Similar observations can be made for the Siberian and Wyoming peridotites, an Archaean age for the Siberian lithospheric keel being
supported by Archaean Re-Os model age and isochron systematics for eclogite xenoliths that are dispersed through the Siberian lithospheric keel (Pearson et al., 1995d). This coincidence of major crust building and the oldest peridotite TRD ages has been used to propose that major crust building and lithospheric stabilisation took place together from the mid- to late-Archaean (Pearson et al., 1995a). The xenolith TRD age data do not suggest any deep lithospheric mantle beneath cratons prior to ca. 3.5 Ga. In contrast, Nagler et al. (1997) found chromites within crustal ultrabasic rocks from the Zimbabwe craton that give TRD ages of up to 3.8 Ga. These ages are in excess of their emplacement ages and Nagler et al. (1997) interpreted them to reflect interaction with old lithospheric mantle during magma ascent into the crust, thus suggesting the presence of CLM beneath this region at ca. 3.8 Ga or before. The thickness of this ancient lithospheric mantle is not clear and further work is needed to investigate whether such material was present beneath the most ancient crustal fragments of other cratons at this time. The abundance and wide distribution of xenolithbearing kimberlites intruding the southern African crust, both on and off-craton, provides an opportunity to study the age relationships between cratonic and circum-cratonic mantle. Analysis of xenoliths suites intruding Proterozoic basement, off-craton in Namibia, to the West of the Kaapvaal craton, and in East Griqualand, S.E. of the craton margin (Pearson et al., 1998c) give TRD ages that range up to 2.4 Ga (Fig. 16), with no indication of Archaean ages. The oldest TRD ages for both off-craton xenolith suites match well the age of basement in each area, at ca. 2.1 Ga, showing strong coupling between mantle and crustal evolution. Even though the East Griqualand kimberlites sample mantle from within 100 km of the craton margin (Nixon et al., 1983), they are clearly distinct in age from the cratonic peridotites erupted in N. Lesotho, indicating a sharply defined craton margin in the mantle. The mid-Archaean ages of some N. Lesotho xenoliths indicate no progressive age decrease towards the edge of this part of the Kaapvaal craton and may imply a sharp tectonic contact, compatible with the abrupt age change in the lithospheric rocks. Recently, Pearson et al. (1998b) have found evidence for Proterozoic ages in peri-
D.G. Pearson/Lithos 48 (1999) 171-194
I
r
I
----1 T RD Ga
Fig. 16. Histograms comparing frequency distributions of TRD ages for peridotite xenoliths from the Kaapvaal craton (Walker et al., 1989a; Pearson et al., 1995a), Namibia (Pearson et al., 1994), and East Griqualand (Pearson et al., 1998c).
dotites from the Vitim region, surrounding the southern margin of the Siberian craton, that concur with Proterozoic crustal basement ages (Kovalenko et al., 1990). In contrast to the coherent crust-mantle relations observed above, Handler et al. (1997) found that some spinel peridotite xenoliths erupted through Paleozoic crust in SE Australia were of Proterozoic age, indicating the persistence of fragments of ancient lithosphere beneath areas of younger tectonised crust. Os isotopes provide some evidence of postArchaean lithospheric addition in the Kaapvaal craton. Samples from the Premier kimberlite, South Africa, consistently give post-Archaean ages of ca. 2 Ga (Pearson et al., 1995a; Carlson et al., in press). The Premier kimberlite erupts through the outcrop
187
ring of the Bushveld intrusion that formed close to 2 Ga and it seems likely that a major new addition to the lithosphere occurred beneath the region at this time (Richardson et al., 1993; Carlson et al., 1998). This possibility is supported by the occurrence of Bushveld erlichmenites (Hart and Kinloch, 1990) with lS7Os/188Os in the range of the Premier peridotites, that show evidence of mantle extraction at 2 Ga. The Os isotope composition of these grains presumably reflects that of the dominant component contributing to Bushveld magmatism in this period. In contrast, osmiridiums, laurites and erlichmenites from the Witwatersrand basin show evidence of grains as old as 3.3 Ga, the same age as the postulated maximum lithospheric mantle age in the main Kaapvaal craton root, south of the Limpopo belt (Pearson et al., 1995a). Further studies are in progress, aimed at characterising possible lateral variations in lithospheric age across the Kaapvaal craton to better address models of craton accretion. One significant result already evident is the presence of lithospheric peridotites with TRD ages as old as 3.6 Ga below the Limpopo Belt (Carlson et al., in press), suggesting that the Limpopo Belt is a shallow feature overlying a cratonic root that continues North, into Zimbabwe. Garnet peridotite xenoliths sampled most commonly by kimberlites have mineralogies amenable to thermobarometry, e.g., Finnerty and Boyd (1987). This potentially allows the age variation of lithospheric mantle with depth across a craton and into the surrounding circum-craton areas to be studied (Fig. 17). Plots of T~I) age vs. depth for southern African xenoliths show little correlation, with shallow, spinel-facies mantle in some pipes having similar ages to samples derived from close to the base of the lithosphere (Fig. 17). A significant result for Re-Os studies has been the finding that the hightemperature xenolith suite from kimberlites also give numerous ancient, in some cases, Archaean ages, suggesting that they have been a coherent part of the lithosphere for large periods of time (Walker et al., 1989a; Pearson et al., 1995a). This contrasts with earlier models invoked on petrological and isotopic grounds (Nixon and Boyd, 1973; Richardson et al., 1985). If the oldest xenolith TRI~ ages approximate to the actual mantle formation ages, the lack of clear age
D.G. Pearson / Lithos 48 (1999) 171-194
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N
W
TBL Fig. 17. Schematic cross-section across southern Africa showing TRI~ ages (same data sources as Fig. 16) next to the approximate level of lithospheric derivation for selected xenoliths from individual kimberlite pipes (from mineral barometry). FL m Farm Louwrencia; J Jagersfontein; F - - Finsch; K - - Kimberley; P - - Premier; N L - - North Lesotho; R - - Ramatseliso; A - - Abbotsford.
distribution with depth in both on- and off-craton lithosphere may indicate rapid formation of lithospheric mantle keels, possibly related to plumes (Pearson et al., 1995a). While Nagler et al. (1997) suggest gradual growth of the CLM as a whole, their modelling does not preclude bursts of lithosphere generation in particular regions. In detail, the question of the time scale of generation of lithospheric keels needs to be better constrained, in particular, the proportion of CLM stabilised to different depths.
3.3.4. Re-Os systematics in orogenic peridotites Orogenic peridotites provide the opportunity to examine CLM longevity and stability in a different setting than cratons and their surroundings. As mentioned above, these massifs of peridotite are generally less isotopically disturbed than cratonic xenoliths. In addition, massif peridotites are petrologically distinct from cratonic peridotitic mantle (Boyd, 1989; Menzies and Dupuy, 1991a) and probably reflect different mantle differentiation styles. One of the most significant observations of Re-Os systematics in orogenic peridotites is the strong coherence
between major element chemistry and Os isotope systematics (Reisberg and Lorand, 1995; Reisberg et al., 1991; Burnham et al., 1998). Reisberg and Lorand (1995) observed clear correlations between 1870S/1880S and A120 3 for both Pyrenean and Ronda peridotites (Fig. 18). Re and S correlated less well. On the basis that A1 should be less easily perturbed than Re or S during mantle metasomatism, and the similar compatibility of Re to A1 during mantle melting, Reisberg and Lorand (1995) used the A120 3 -- 1 8 7 0 S / 1 8 8 0 S c o r r e l a t i o n as an isochron analogue, produced by a single melting event, to constrain the initial ~87Os/]SSOs of the peridotite suite by extrapolating A120 3 to zero. This value is then used to calculate the model age of mantle melting assuming a Re/Os of zero (essentially a TRD age). This produced a model Re depletion age of ca. 2.4 Ga for Pyrenean peridotites. Extrapolation of AlzO3-]SVOs/]S8Os correlations in peridotites assumes that both A1 and Re will be exhausted simultaneously during mantle melting. A detailed study of Pyrenean peridotites by Burnham et al. (1998) reveals good correlations for both Re
189
D.G. Pearson/Lithos 48 (1999) 171-194
1~
0.115
Fig. 18. A120 3 (wt.%) v s . 187Os/188Os correlation (R2 =0.89) for Pyrenean peridotites (Reisberg and Lorand, 1995; Burnham et al., 1998) compared to much more scattered relationship for Namibian peridotites (Pearson et al., 1994).
and S with 187Os/1880s (provided that metasomatised samples with anomalously low C u / O s are excluded), clearly showing that Re and S are both depleted before A1 in this suite, and indicating strong Re control by sulfide (Fig. 19). If estimates of initial 1870s/1880s are made by extrapolation of either Re-187Os/188Os or S - 187Os/lg8os trends, a considerably higher value is obtained than using A120 3 (Fig. 19), leading to significantly younger Re depletion ages (initial 187Os/~88Os values from Re and S correlations are within error of each other). It is unlikely that extrapolation of A120 3 --187Os/188Os correlations will be a valid procedure in any orogenic peridotites. Re appears to be controlled by sulfide in these environments and sulfide is exhausted (Lorand, 1991) well before the last significant Al-bearing phase, enstatite, with up to 5 % A12O3 in some spinel-facies peridotites. Hence, ages based on A1-Os isotope correlations will be too old. No kimberlite-borne xenolith suites have been found so far that show A120 3 correlations (e.g., see the scattered trend for Namibian peridotites in Fig. 18). This may reflect either a very different style of mantle differentiation in these samples, or, more complex disturbance of Re-Os systematics, or a combination of both. For these sample suites, frequency distributions of TRD ages from whole rocks, or model ages from chromites probably give the most meaningful results.
1870s/1880si 0.116
= 0.116
D
Fig. 19. Re-S and AI20 3 vs. 187Os/188Os plots for Pyrenean peridotite massif samples. Solid squares are "unmetasomatised" samples, open squares "metasomatised" on the basis of Cu/S values (data from Burnham et al., 1998). Note that TRD values for extrapolated initial Os isotope ratios are similar for Re and S correlations and considerably younger than the TRD model age calculated from the initial Os isotope composition obtained from the AI20 3 v s . 187Os/188Os correlation.
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D.G. Pearson / Lithos 48 (1999) 171 - 194
Obtaining lithosphere stabilisation ages from massif peridotites appears to be possible by screening samples for metasomatism using C u / S relationships and determining initial lS7Os/lSSOs values from either Re--lS7Os/lSSOs or S-1870s/1880s correlations (Burnham et al., 1998). The Re depletion model age of 1.9 _+ 0.3 Ga obtained by Burnham et al. (1998) using this method coincides with a major period of crustal growth in the Pyrenean region at 1.86 Ga, but post-dates an older major crustal growth event at ca. 2.7 Ga, suggesting that original CLM associated with the older event has either been removed, or modified. As noted by Burnham et al. (1998), the ages given by orogenic peridotites do not provide direct information on the age of mantle deeper than the spinel-garnet transition zone in most instances. Despite the sometimes unclear relationship of orogenic peridotites to the surrounding crustal rocks, they are important groups of rocks for documenting lithospheric mantle accretion and the Os isotopic evolution of the Earth's mantle. 3.3.4.1. E c l o g i t e x e n o l i t h s . Eclogite xenoliths erupted by kimberlite pipes represent important components in the lithospheric mantle beneath many cratons and circum-cratonic regions. Their origin is currently contentious, e.g., Jacob et al. (1994), Snyder et al. (1997), but the possibility that they may represent remnants of ancient subducted oceanic lithosphere (Jagoutz et al., 1984; MacGregor and Manton, 1986; Jacob et al., 1994) means that if they can be dated accurately we may be able to constrain whether deep subduction operated in the Archaean. Dating eclogites using incompatible element-based isotope systems is as fraught with difficulty as dating peridotites (Snyder et al., 1993). Probably the most reliable "age" for eclogites using N d - S r - P b systems is the 2.76 Ga pyroxene Pb-Pb isochron reported by Jacob et al. (1994). Recently the Re-Os system has been applied to this problem (Pearson et al., 1995d; Menzies et al., 1998; Shirey et al., 1998). The relatively low Os contents of many eclogites compared to peridotites nominally makes them more susceptible to metasomatism than cratonic peridotites. However, this is counterbalanced by their radiogenic Os isotope compositions and their often very high Re/Os values that steeply diverge from the mantle evolution line (Fig. 20) such that major disturbance is required
lz9/89 a~
4.0 3.0 2.0
1.0
Fig. 20. Re-Os evolution of a suite of diamondiferous eclogites from Udachnaya, Siberia. Evolution steeply diverge from the chondritic evolution line and converge in the area between 2.5 to 3 Ga.
to dramatically affect Re-Os model age systematics. The supra-chondritic lS7Os/lSSOs of eclogites means that TMA Re-Os model ages are used rather than Tm~ ages. A suite of diamondiferous eclogite xenoliths from the Udachnaya kimberlite, Siberia, give whole-rock Re-Os model ages of 2.6 to 3.4 Ga (one sample 6.5 Ga), with Os evolution lines that intersect at ca. 2.7 Ga (Fig. 20), within error of the 2.9 _+ 0.4 Ga whole rock Re-Os isochron defined by these samples Pearson et al., 1995d). The Re-Os model ages for the Udachnaya eclogites agree well with the whole rock isochron and Pb-Pb cpx isochron for other Udachnaya diamondiferous eclogites (Jacob et al., 1994). This agreement is strong evidence that deep Archaean subduction may have operated, if these rocks are former oceanic crustal fragments, or residues from slab melting (Ireland et al., 1994). The elevated initial Os isotopic composition of the Re-Os isochron defined by Pearson et al. (1995d) may indicate a significant pre-history for the eclogite precursors.
4. Implications and summary
Some of the major discoveries made by isotopic dating of continental roots are discussed below.
D.G. Pearson/Lithos 48 (1999) 171-194
Early Sr-Nd isotope studies (e.g., Menzies and Murthy, 1980; Richardson et al., 1984) noted the record of ancient incompatible element enrichment in cratonic roots that must have evolved over billions of years to produce enriched isotopic signatures. S m - N d and Re-Os isotopic studies clearly document the fact that the CLM beneath most cratons has been isolated from the convecting mantle since at least the late- to middle-Archaean (Richardson et al., 1984; Walker et al., 1989a; Carlson and Irving, 1994; Carlson et al., in press; Pearson et al., 1995a,c; Chesley et al., in press) and possibly since the early Archaean (Nagler et al., 1997) for some cratons. No unequivocal Hadean signatures have so far been recorded. The age of CLM appears broadly similar to that of the initiation of the main crust formation events on the Siberian, Kaapvaal and Wyoming cratons. This suggests either a genetic link, or implies that large fragments of continental crust need protective deep lithospheric keels to survive. The correspondence of ancient crust underlain by ancient mantle to great depths (200 km) on craton implies long-term physical coupling of crust plus mantle in these regions that appears very robust to geological processes. Moreover, the correspondence of Proterozoic mantle beneath Proterozoic crust in several circum-cratonic regions (Pearson et al., 1994, 1998a,b) testifies to the robustness of circum-cratonic mantle in some instances, perhaps protected by very thick adjacent cratonic keels. Studies of other, predominantly spinel-peridotite xenolith suites (Cohen et al., 1996; Handler et al., 1997) and orogenic peridotite massifs (Reisberg and Lorand, 1995; Burnham et al., in press), show that continental mantle can survive for billion year periods, at least at shallow levels, in more complex tectonic settings. No convincing age structure with lithospheric depth has so far been found that gives a clear view of how cratonic roots have been constructed, perhaps indicating rapid formation of large thick keels, either by rapid arc accretion, or plume-driven differentiation. Pearson et al. (1995a) and Carlson et al. (in press) have pointed out the possibility of new lithospheric material being added to the centre of the Kaapvaal root at ca. 2 Ga during the formation of the Bushvled complex. More detailed studies are in progress, also aimed at trying to define lateral age
191
variation within cratons (Carlson et al., in press). Later additions of younger lithospheric material to the root of the Tanzanian lithosphere have been suggested by Chesley et al. (in press) on the basis of much younger (0.3 to 1.0 Ga) TRD ages obtained from xenoliths with > 120 km equilibration depths. The Re-Os system is a powerful tool for distinguishing ancient lithosphere in complex tectonic areas (Handler et al., 1997; Hassler and Shimizu, 1998) and in constraining continental keel evolution. More studies of well constrained xenolith suites and orogenic peridotites are required from different cratons and orogenic belts to further our understanding of how continents are built and evolve.
Acknowledgements The author thanks R.W. Carlson, S.B. Shirey, F.R. Boyd and P.H. Nixon for guidance on many issues relating to the material covered in this manuscript and to G. Nowell, R. Rudnick and R. Carlson for helpful reviews.
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Reisberg, L., Lorand, J.P., 1995. Longevity of sub-continental mantle lithosphere from osmium isotope systematics in orogenic peridotite massifs. Nature 376, 159-162. Reisberg, L., Zindler, A., 1986. Extreme isotopic variations in the upper mantle: evidence from Ronda. Earth Plan. Sci. Lett. 81, 29-45. Reisberg, L., Zindler, A., Jagoutz, E., 1989. Further Sr and Nd isotopic results from peridotites of the Ronda ultramafic complex. Earth Planet. Sci. Lett. 96, 161-180. Reisberg, L.C., Allegre, C.J., Luck, J.-M., 1991. The Re-Os systematics of the Ronda ultramafic complex in southern Spain. Earth Planet. Sci. Lett. 105, 196-213. Richardson, S.H., Gurney, J.J., Erlank, A.J., Harris, J.W., 1984. Origin of diamonds in old enriched mantle. Nature 310, 198-202. Richardson, S.H., Erlank, A.J., Hart, S.R., 1985. Kimberlite-borne garnet peridotite xenoliths from old enriched subcontinental lithosphere. Earth Planet. Sci. Lett. 75, 116-128. Richardson, S.H., Harris, J.W., Gurney, J.J., 1993. Three generations of diamonds from old continental mantle. Nature 366, 256-258. Rudnick, R.L., Ireland, T.R., Gehrels, G., Irving, A.J., Chesley, J.T., Hanchar, J.M., 1998. Dating mantle metasomatism: U-Pb geochronology of zircons in cratonic mantle xenoliths from Montana and Tanzania. Ext. Abstr. 7th Int. Kimb. Conf. Cape Town, pp. 754-756. Sambridge, M.S., Lambert, D.D., 1997. Propagating errors in decay equations: examples from the Re-Os isotopic system. Geochim. Cosmochim. Acta 61, 3019-3024. Scharer, U., Corfu, F., Demaiffe, D., 1997. U-Pb and Lu-Hf isotopes in baddeleyite and zircon megacrysts from the Mbuji-Mayi kimberlite: constraints on the subcontinental mantle. Chem. Geol. 143, 1-16. Shimizu, N., Sobolev, N.V., 1995. Young peridotitic diamonds from the Mir kimberlite pipe. Nature 375, 394-397. Shimizu, N., Pokhilenko, N.P., Boyd, F.R., Pearson, D.G., 1997a. Geochemical characteristics of mantle xenoliths from the Udachnaya kimberlite pipe. Russ. J. Geol. Geophys. 38, 194205. Shimizu, N., Sobolev, N.V., Yefimova, E.S., 1997b. Chemical heterogeneities of inclusion garnets and juvenile character of peridotitic diamonds from Siberia. Russ. J. Geol. Geophys. 38, 356-372. Shirey, S.B., Walker, R.J., 1998. The Re-Os isotope system in cosmochemistry and high-temperature geochemistry. Annu. Rev. Earth Planet. Sci. 26, 423-500. Shirey, S.B., Carlson, R.W., Gurney, J.J., Herden, L.V., 1998. Re-Os systematics of eclogites from Roberts Victor: implications for diamond growth and Archean tectonic processes. Ext. Abstr. 7th Int. Kimb. Conf. Cape Town, pp. 808-810.
Smoliar, M.I., Walker, R.J., Morgan, J.W., 1996. Re-Os ages of Group IIA, IIIA, IVA and IVB iron meteorites. Science 271, 1099-1102. Sneeringer, M., Hart, S.R., Shimizu, N., 1984. Strontium and samarium diffusion in diopside. Geochim. Cosmochim. Acta 48, 1589-1608. Snow, J.E., Reisberg, L., 1995. Erratum of "Os isotopic systematics of the MORB mantle; results from altered abyssal peridotites". Earth Planet. Sci. Lett. 136, 723-733. Snyder, G.A., Jerde, E.A., Taylor, L.A., Halliday, A.N., Sobolev, V.N., Sobolev, N.V., 1993. Nd and Sr isotopes from diamondiferous eclogites, Udachnaya kimberlite pipe, Yakutia, Siberia: evidence of differentiation in the early Earth?. Earth Planet. Sci. Lett. 118, 91-100. Snyder, G.A., Taylor, L.A., Crozaz, G., Halliday, A.N., Beard, B., Sobolev, V., Sobolev, N., 1997. The origins of Yakutian eclogite xenoliths. J. Pet. 38, 85-113. Taylor, W.R., Bulanova, G.P., Milledge, H.J., 1995. Quantitative nitrogen aggregation study of some Yakutian diamonds: constraints on the growth, thermal and deformation history of peridotitic and eclogitic diamonds. Ext. Abstr. 6th Int. Kimb. Conf. Novosibirsk, pp. 608-610. Thalhammer, O.A.R., Prochaska, W., Muehlhaus, H.W., 1990. Solid inclusions in chrome-spinels and platinum group element concentrations from the Hochgroessen and Kraubath ultramafic massifs (Austria). Contrib. Mineral. Petrol. 105, 66-80. Walker, R.J., Morgan, J.W., 1989. Rhenium-osmium isotope systematics of carbonaceous chondrites. Science 243, 519-522. Walker, R.J., Carlson, R.W., Shirey, S.B., Boyd, F.R., 1989a. Os, Sr, Nd, and Pb isotope systematics of southern African peridotite xenoliths: implications for the chemical evolution of subcontinental mantle. Geochim. Cosmochim. Acta 53, 15831595. Walker, R.J., Shirey, S.B., Hanson, G.N., Rajamani, V., Horan, M.F., 1989b. Re-Os, Rb-Sr and O isotopic systematics in of the Kolar schist belt, Karnataka, India. Geochim. Cosmochim. Acta 53, 3005-3013. Zhuravlev, A.Z., Laz'ko, Y.Y., Ponomarenko, A.I., 1991. Radiogenic isotopes and REE in garnet peridotite xenoliths from the Mir kimberlite pipe, Yakutia. Geokhimiya 7, 982-994. Zindler, A., Hart, S.R., 1986. Chemical geodynamics. Annu. Rev. Earth Planet. Sci. 14, 493-571. Zindler, A., Jagoutz, E., 1988. Mantle cryptology. Geochim. Cosmochim. Acta 52, 319-333. Zindler, A., Staudigel, H., Hart, S.R., Enders, R., Goldstein, S., 1983. Nd and Sr isotopic study of a mafic layer from the Ronda ultramafic complex. Nature 304, 226-230.
LITHOS ELSEVIER
Lithos 48 (1999) 195-216
Nature of the mantle roots beneath the North American craton" mantle xenolith evidence from Somerset Island kimberlites S.S. Schmidberger *, D. Francis Earth and Planetary Sciences, McGilI University, 3450 University Street, Montreal, Quebec, Canada H3A 2A7
Received 23 March 1998; received in revised form 11 January 1999; accepted 12 January 1999
Abstract The recently discovered Nikos kimberlite on Somerset Island, in the Canadian Arctic, hosts an unusually well preserved suite of mantle xenoliths dominated by garnet-peridotite (lherzolite, harzburgite, dunite) showing coarse and porphyroclastic textures, with minor garnet-pyroxenite. The whole rock and mineral data for 54 Nikos xenoliths indicate a highly refractory underlying mantle with high olivine forsterite contents (ave. Fo = 92.3) and moderate to high olivine abundances (ave. 80 wt.%). These characteristics are similar to those reported for peridotites from the Archean Kaapvaal and Siberian cratons (ave. olivine Fo = 92.5), but are clearly distinct from the trend defined by oceanic peridotites and mantle xenoliths in alkaline basalts and kimberlites from post-Archean continental terranes (ave. olivine Fo = 91.0). The Nikos xenoliths yield pressures and temperatures of last equilibration between 20 and 55 kb and 650 and 1300~ and a number of the peridotite nodules appear to have equilibrated in the diamond stability field. The pressure and temperature data define a conductive paleogeotherm corresponding to a surface heat flow of 44 m W / m 2. Paleogeotherms based on xenolith data from the central Slave province of the Canadian craton require a lower surface heat flow ( ~ 40 m W / m 2) indicating a cooler geothermal regime than that beneath the Canadian Arctic. A large number of kimberlite-hosted peridotites from the Kaapvaal craton in South Africa and parts of the Siberian craton are characterized by high orthopyroxene contents (ave. Kaapvaal 32 wt.%, Siberia 20 wt.%). The calculated modal mineral assemblages for the Nikos peridotites show moderate to low contents of orthopyroxene (ave. 12 wt.%), indicating that the orthopyroxene-rich mineralogy characteristic of the Kaapvaal and Siberian cratons is not a feature of the cratonic upper mantle beneath Somerset Island. 9 1999 Elsevier Science B.V. All rights reserved. Keywords: Canadian craton; Kimberlite; Mantle root; Mantle xenolith; Peridotite; Somerset Island
1. Introduction Global seismic t o m o g r a p h y has shown that cold mantle roots with high seismic velocities underlie
* Corresponding author. E-mail: [email protected]
most Archean cratons to depths of at least 350 to 400 k m (Jordan, 1988; Grand, 1994). Kimberlite-hosted mantle xenoliths are the only direct samples of these mantle roots beneath Archean cratonic areas and thus provide constraints on their composition and structure. Studies of such xenoliths in kimberlites from South Africa have shown the highly refractory nature of the mantle roots beneath the Archean Kaapvaal
0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All rights reserved. PII: S0024-4937(99)00029-8
196
S.S. Schmidberger, D. Francis/Lithos 48 (1999) 195-216
craton, with high olivine forsterite contents ( M g / (Mg + Fe) greater than 0.91; e.g., Cox et al., 1973; Nixon et al., 1981; Boyd, 1987). A large number of these mantle nodules are characterized by high modal orthopyroxene (up to 45 wt.%; Boyd and Canil, 1997) and low M g / S i ratios (Boyd et al., 1997). The occurrence of orthopyroxene-rich mineral assemblages has also been reported for the Siberian craton (ave. O p x = 20 wt.%; Boyd et al., 1997). These compositional characteristics indicate that the deepseated mantle roots of Archean cratons are chemically distinct from the upper mantle beneath oceanic
and post-Archean crustal terranes (Boyd, 1989; Boyd et al., 1997; Shi et al., 1998). Whether the orthopyroxene-rich character reported for the mantle roots beneath the Kaapvaal and Siberian cratons is characteristic of cratonic mantle roots in general, however, has yet to be established. In this paper, we present geochemical data for a suite of mantle xenoliths from the Nikos kimberlite on Somerset Island in the Canadian Arctic. Mineral chemistry and modal mineral analysis provide constraints on the nature of the mantle roots beneath the Canadian craton and enable a comparison with the
I
/ /
,f--i
/
/
/
Fig. 1. Geological map of Somerset Island (after Steward, 1987) showing kimberlite locations. Legend: light gray, Paleozoic cover rocks; striped, Late Proterozoic cover rocks; dark gray, Precambrian basement; bold lines, normal faults.
197
S.S. Schmidberger, D. Francis/Lithos 48 (1999) 195-216
compositional characteristics reported Archean Kaapvaal and Siberian cratons.
for
the
2. Geology Somerset Island is part of the Innuitian tectonic province on the northern margin of the North American continent (Trettin et al., 1972). The local stratigraphy comprises middle Proterozoic to early Paleozoic sedimentary sequences that overlie the crystalline Precambrian basement of the Boothia Uplift
(Steward, 1987). The Precambrian basement represents a northward salient of the Canadian shield that was deformed and faulted in the late Proterozoic to early Paleozoic, possibly related to compression associated with the Caledonian Orogeny in northern Europe and Greenland (Okulitch and Trettin, 1991). Granulite facies gneisses from the crystalline basement of the Boothia Uplift yield zircon dates between 2.5 and 2.2 Ga for their protoliths, while S m - N d model ages of 3.0 to 2.2 Ga suggest the presence of reworked Archean crustal material in these gneisses (Frisch and Hunt, 1993).
Table 1 Major and trace element analyses of kimberlites The major and trace elements were analyzed by X-ray fluorescence analysis at McGill University with a Philips PW 2400 spectrometer. The major elements and Ba, V, Co, Cr, and Ni were analyzed on fused discs using a c~-coefficient technique with an analytical precision of less than 0.06 wt.% (1 SD). Total Fe is given as FeO. Other trace elements were analyzed on pressed pellets using a Rh Kb Compton scatter matrix correction with an analytical precision of 5%. Sample Rock
NK3-K1 Kimberlite
Major elements in wt. % SiO 2 19.85 TiO 2 2.06 A120 3 2.20 FeO 7.06 MnO 0.14 MgO 19.97 CaO 21.58 Na20 0.19 K20 1.00 P205 0.64 H20 1.43 CO 2 22.78 Total 98.90 CaCO3 38.52 Trace elements in ppm Ba 2694 Rb 72 Sr 1299 Th 18.2 U 0 Zr 139 Nb 166 Y 9.3 Cr 1366 Ni 672 Co 52 V 153 Sc 28
NK3-K2 Kimberlite
NK3-K3 Kimberlite
NK3-K4 Kimberlite
NK3-K5 Kimberlite
25.05 2.15 2.81 8.13 0.16 26.12 15.34 0.14 0.66 0.64 5.00 12.68 98.88 27.38
23.21 1.62 2.03 6.99 0.15 23.07 17.57 0.06 0.55 0.92 5.07 17.10 98.35 31.36
22.72 1.73 1.90 7.32 0.14 23.03 18.90 0.09 0.30 0.83 8.55 13.19 98.71 30.00
23.62 1.51 1.64 7.26 0.15 25.59 16.61 0.10 0.59 0.85 0.00 20.96 98.88 29.65
2231 46 1072 17.4 1.4 162 169 11.3 1586 817 64 151 16
2972 30 1647 22.3 0 163 198 11.8 1721 861 59 136 15
3007 22 2233 23.1 0 146 190 9.5 1526 855 64 140 19
2445 38 1418 18.7 0 147 179 10.4 1362 917 65 126 23
198
s.s. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
Other kimberlite occurrences on Somerset Island and their mantle xenoliths have been previously de-
scribed (e.g., Mitchell, 1977; Jago and Mitchell, 1987; Fig. 1). The kimberlite pipes were emplaced
(a)
Fig. 2. Photomicrographs of xenoliths from the Nikos kimberlite showing (a) coarse texture in peridotite, (b) porphyroclastic texture in peridotite, and (c) coarse texture in pyroxenite. Upper photographs with plane polars, lower photographs with crossed polars.
S.S. Schmidbergrr, D. Francis/Lithos 48 (19991 195-216
199
Fig. 2 (continued).
during the Cretaceous along a major fault system related to the development of the Boothia Uplift (Mitchell, 1975). U-Pb dates on perovskite indicate
kimberlite formation ages between 88 and 105 Ma (Heaman, 1989; Smith et al., 1989). Kimberlite emplacement coincides with major compressive defor-
200
S.S. Schmidberger, D. Francis /Lithos 48 (1999) 195-216
Fig. 2 (continued).
mation in the southeastern Arctic Islands induced by rifting that preceded sea-floor spreading in the Labrador Sea and Baffin Bay and the associated
rotation of Greenland away from the North American continent that began in the early Cretaceous (Okulitch and Trettin, 1991). The timing of kimber-
S.S. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
lite emplacement on Somerset Island coincides with a world wide period of kimberlite activity in the Cretaceous (Nixon, 1987).
3. Kimberlite host
Previous field work and petrographic studies have shown that the majority of the Somerset kimberlites are brecciated diatremes or hypabyssal roots zones (Mitchell and Meyer, 1980), consisting of fragments of kimberlite host, country rock, and mantle-derived xenocrysts. Establishing the compositions of the liquids for such kimberlites is problematic because of the difficulty of accounting for the country rocks and xenocrysts present in the kimberlite breccia. Magmatic kimberlite, containing less than 15 vol.% of clasts larger than 4 mm, is rare on Somerset Island (Mitchell and Meyer, 1980; Mitchell, 1986). The recently discovered Nikos kimberlite (Pell, 1993) outcrops along a steep cliff on the eastern coast of Somerset Island (73~ and 90~ Fig. 1) and consists of three individual pipes that were sampled during the summer of 1996. Petrographic observations of the kimberlite samples indicate that one of these pipes (NK3) is characterized by a non-brecciated, magmatic texture. The magmatic kimberlite exhibits a porphyritic microcrystalline texture containing phenocrysts of olivine, phlogopite, and spinel in a very fine-grained carbonaterich matrix. Two generations of olivine can be identified, rounded olivine phenocrysts ( > 1 mm) that most probably crystallized prior to the intrusion of the kimberlite and small euhedral to subhedral olivines ( < 1 mm). Garnet megacrysts (up to 5 mm) may represent xenocrysts derived by fragmentation of garnet peridotite xenoliths or be a liquidus phase at high pressure in the kimberlite magma (Mitchell, 1978; Mitchell and Meyer, 1980). The microcrystalline groundmass consists of calcite, serpentine, perovskite, and apatite. Calcite occurs as aggregates of tabular euhedral crystals or as sub-parallel laths, which are deflected around large olivine crystals, indicating their primary magmatic nature. Serpentine occurs as spherical microcrystalline segregations and as an alteration product of olivine marginally replacing these phenocrysts.
201
The whole rock analyses of kimberlite NK3 (n = 5) indicate an extremely carbonate rich composition, with CaCO 3 contents between 27 and 39 wt.% (ave. 31 wt.%), low SiO 2 abundances (20-25 wt.%), and a strong enrichment in incompatible trace element contents ( B a - 2 2 0 0 - 3 0 0 0 ppm; S r = 1100-2200 ppm; Table 1). The high carbonate contents of the kimberlitic liquid indicate compositions intermediate between kimberlite (ave. CaCO3 = 14 wt.%; Mitchell, 1986; Ringwood et al., 1992) and carbonatite (CaCO 3 = 50-80 wt.%; Woolley and Kempe, 1989), in keeping with recent experimental studies that have shown that a continuous spectrum of melt compositions from carbonatite to kimberlite can be produced by increasing degree of melting at pressures on the order of 60 kb (Dalton and Presnall, 1997).
4. Mantle xenoliths
The Nikos kimberlite hosts an unusually well preserved suite of large (10-20 cm) mantle-derived xenoliths, 54 of which were collected and analyzed in this study. The Nikos xenolith suite is dominated by garnet-peridotites (about 90%) comprising lherzolites, harzburgites, and lesser dunites. Also present are small numbers of pyroxene-rich nodules that are classified as garnet-pyroxenite rather than eclogite (Dawson, 1980; Hatton and Gurney, 1987) because of their low modal garnet (10-15 wt. %) and A12 O3 contents (5-10 wt.%), and the low jadeite component in clinopyroxene (Na20 < 1.6 wt.%). The majority of the peridotite nodules have textures ranging from coarse equant to coarse tabular (Fig. 2a), based on the textural classification for mantle-derived rocks of Harte (1977). Large subhedral crystals of well preserved and relatively strainfree olivine (up to 10 mm) and orthopyroxene (ave. 2-5 mm) dominate the mineral assemblage. Clinopyroxene occurs as emerald green anhedral crystals with smooth grain boundaries (1-3 mm). Purple red garnet occurs as large porphyroclasts (ave. 5 mm) and is variably surrounded by kelyphitic rims of phlogopite and small spinel crystals. A small number of peridotite xenoliths exhibit porphyroclastic textures ( < 10%; Fig. 2b), characterized by large porphyroclasts (up to 10 mm) of strained olivine
Table 2 Representative analyses of bulk xenoliths LOI: loss on ignition. Total Fe is given as FeO and Mg # = M g / ( M g +Fe). Lherz: lherzolite, Harz: harzburgite, Pyrox: pyroxenite, porphyr: porphyroclastic. Modes were calculated using the whole rock compositions and a high-pressure peridotite norm recipe. Analytical procedure as in Table 1. Sample Rock Texture
NK1-5 Lherz coarse
NK2-3 Lherz coarse
Major elements in wt. %. SiO 2 42.28 42.46 TiO 2 0.07 0.09 A120 3 1.95 2.90 FeO 7.74 7.21 MnO 0.12 0.13 MgO 41.49 41.87 CaO 1.44 1.98 Na20 0.06 0.15 K20 0.08 0.19 P2 05 0.01 0.02 Cr20 3 0.85 1.04 NiO 0.30 0.31 LOI 3.50 1.77 Total 99.89 100.13 Mg # 0.905 0.912
NK2-10 Lherz coarse
NK3-20 Lherz coarse
NK3-25 Lherz coarse
NK1-2 Harz coarse
NK1-3 Harz coarse
NK1-6 Harz coarse
NK1-7 Harz porphyr
NK1-17 Harz coarse
NK1-18 Harz coarse
NK2-7 Pyrox coarse
NK3-1 Pyrox coarse
NK3-17 Pyrox coarse
41.54 0.03 1.25 7.43 0.11 45.53 1.22 0.07 0.05 0.04 0.53 0.32 1.84 99.97 0.916
43.19 0.10 3.21 7.58 0.13 37.50 3.21 0.35 0.14 0.02 0.67 0.28 3.30 99.68 0.898
41.42 0.21 4.28 7.41 0.13 39.46 2.13 0.09 0.52 0.04 1.09 0.25 2.81 99.85 0.905
41.77 0.03 1.31 7.39 0.11 44.44 1.11 0.10 0.03 0.02 0.52 0.32 2.71 99.85 0.915
40.81 0.03 1.33 7.42 0.11 44.03 0.82 0.01 0.04 0.02 0.60 0.33 3.89 99.42 0.914
40.37 0.02 1.25 7.10 0.10 43.41 0.41 0.00 0.03 0.01 0.68 0.33 5.85 99.57 0.916
41.24 0.03 1.57 7.06 0.10 43.55 0.72 0.00 0.02 0.01 0.70 0.31 4.31 99.62 0.917
41.22 0.01 0.81 7.05 0.11 45.40 0.49 0.08 0.03 0.03 0.68 0.31 3.88 100.10 0.920
42.94 0.03 0.79 6.97 0.10 44.93 0.54 0.05 0.03 0.01 0.51 0.35 2.75 100.00 0.920
48.95 0.13 8.05 4.93 0.18 23.69 9.45 0.90 0.11 0.01 1.69 0.38 1.90 100.37 0.895
50.97 0.18 4.71 6.04 0.15 19.44 16.46 0.46 0.11 0.02 0.79 0.09 0.52 99.94 0.852
50.15 0.18 4.89 6.01 0.15 19.48 16.91 0.28 0.09 0.01 0.73 0.09 0.58 99.55 0.852
4~
I
t~
Calculated Oliv Opx Cpx Garn
modes in wt. %. 71.0 69.0 18.1 15.8 6.1 8.6 4.8 6.6
87.8 4.2 5.1 3.0
56.9 22.5 14.2 6.4
60.9 19.5 9.8 9.9
83.5 8.8 4.7 3.0
84.1 9.1 3.4 3.5
82.5 12.3 1.7 3.5
79.2 13.8 2.9 4.1
87.9 7.7 2.3 2.2
80.6 15.1 2.3 2.0
4.4 41.0 39.2 15.4
0 23.6 67.0 9.4
0 22.2 67.6 10.3
S.S. Schmidberger, D. Francis/Lithos 48 (1999) 195-216
with undulose extinction surrounded by strain-free olivine neoblasts (0.1-0.5 mm) with tabular to polygonal equant habits. In these rocks, orthopyroxene occurs as porphyroclasts (2-5 mm) with irregular habit, and clinopyroxene and garnet are optically similar to those found in the coarse peridotites. The pyroxenite nodules show coarse equant textures (Fig. 2c) with large subhedral crystals (2-5 mm) of clinopyroxene and orthopyroxene, and smaller crystals (1 mm) of pale red garnet with a polygonal habit.
5. Analytical data 5.1. Whole rock chemistry Whole rock analyses indicate that the Nikos peridotites are strongly depleted in fusible elements such as Fe, Ti, Ca, A1, and Na compared to estimated primitive mantle compositions (McDonough, 1990" Table 2). The whole rock magnesium numbers (Mg # = M g / ( M g + Fe); Fig. 3) for the lherzolites (ave.
203
Mg # = 0.91), harzburgites (ave. Mg # = 0.92), and dunites (ave. Mg # = 0.92) indicate a shift toward higher values for the harzburgites and dunites consistent with their larger degree of depletion. The Nikos nodules are significantly more refractory than oceanic peridotites and mantle xenoliths derived from beneath post-Archean continental crust (Mg # = 0.890.91; Boyd, 1989). There is a good negative correlation between A1 and Ca, and Mg (Fig. 4a,b), and a rough positive correlation between Ni and Mg (Fig. 4c). Compared to spinel-lherzolites from the Canadian Cordillera (Shi et al., 1998), the late Phanerozoic orogenic belt that borders the western margin of the Canadian shield, the Nikos peridotites contain much lower A120 3 contents (Fig. 5) and higher Mg#s (Fig. 8). This indicates that the mantle roots beneath the Canadian shield are significantly more refractory than the lithospheric mantle beneath the Phanerozoic Cordillera. Spinel-harzburgites occurring in some of the Cordilleran xenolith suites from the southwestern Yukon and northern British Columbia, however, exhibit A1203 contents indistinguishable from those for the Nikos xenoliths (Fig. 5).
Fig. 3. Histogram of whole rock magnesium numbers (Mg # = Mg/(Mg + Fe)) of peridotites, and high-Mg and low-Mg pyroxenites.
204
S.S. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
lherzolites and 0.92 to 0.93 (ave. 0.925) in the harzburgites, indicating higher values for the more refractory nodules (Table 3 for representative analyses). Individual olivine crystals do not exhibit chemical zoning and are homogeneous on thin section scale. There is no compositional difference between the olivines of the coarse and porphyroclastic peridotites. The Somerset olivine Mg#s (ave. 0.923) are similar to those for peridotites from the Kaapvaal and Siberian cratons (ave. 0.925), but somewhat higher than the values reported for the Jericho (ave. 0.913; Kopylova et al., 1999) and the Torrie xeno-
|
|
|
9
b
@
9 9 9
0.3 60 |
i Bi-modal
Fig. 4. Variations of major elements (a) A1203, (b) CaO, (c) NiO with MgO (wt.%) of Nikos peridotites. Primitive mantle composition after McDonough (1990). These refractory harzburgites are associated with a seismically detected hot mantle anomaly (Shi et al., 1998). The pyroxenites, on the other hand, show a large variation in Mg#s. The pyroxenites having high Mg#s between 0.88 and 0.92 (high-Mg pyroxenites) overlap those of the peridotites. The Mg#s for the other group of pyroxenites, however, are significantly lower (Mg # = 0.84-0.85; low-Mg pyroxenites), indicating that they are more Fe-rich than the coexisting peridotite xenoliths (Fig. 3). 5.2. Mineral chemistry 5.2.1. Olivine Olivine in the peridotites is magnesium-rich and ranges in Mg # from 0.91 to 0.93 (ave. 0.921) in the
i i i i i i
U
,i
i
i i I
1 I I
!Cordillera ~ Uni-moda!
i 10
Fig. 5. Histogram of A1203 content (wt.%) of Nikos peridotites compared to data for the bi-modal northern Cordilleran spinelharzburgite and spinel-lherzolite suite and the uni-modal southern Cordilleran spinel-lherzolite suite (Shi et al., 1998). Primitive mantle composition after McDonough (1990).
205
S.S. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
Table 3 Representative analyses of olivines The mineral compositions (wt.%) were determined using a JEOL 8900L electron microprobe at McGill University. The mineral phases were analyzed by wavelength dispersive spectroscopy with an acceleration voltage of 20 kV, beam current of 20 nA, and a beam diameter of 5 txm. On-peak counting times were 20 s, and the background counting times 10 s. Sample Rock
NK1-5 Lherz
NK2-3 Lherz
NK2-10 Lherz
NK3-20 Lherz
NK3-25 Lherz
NK1-2 Harz
NK1-3 Harz
NK1-6 Harz
NK1-7 Harz
NKl-17 Harz
NKI-18 Harz
SiO 2
40.75 8.15 0.12 49.43 0.04 0.04 0.35 98.94 0.915
41.43 7.07 0.10 51.04 0.01 0.00 0.40 100.08 0.928
40.78 7.43 0.10 50.83 0.01 0.01 0.36 99.56 0.924
41.26 8.59 0.09 50.27 0.01 0.00 0.38 100.63 0.912
41.29 8.47 0.11 50.48 0.05 0.02 0.36 100.83 0.914
41.02 7.48 0.10 50.20 0.01 0.01 0.35 99.19 0.923
41.03 7.37 0.10 50.43 0.01 0.01 0.35 99.33 0.924
40.81 7.15 0.10 51.30 0.02 0.02 0.38 99.79 0.927
41.01 7.35 0.10 50.67 0.05 0.04 0.37 99.62 0.925
40.94 7.09 0.10 51.04 0.02 0.01 0.36 99.58 0.928
41.26 7.21 0.10 50.88 0.03 0.04 0.43 99.99 0.926
0.993 0.151 0.002 1.845 0.000 0.000 0.007 3.992
1.000 0.174 0.002 1.816 0.000 0.000 0.007 4.000
0.998 0.171 0.002 1.819 0.001 0.000 0.007 3.997
1.004 0.153 0.002 1.832 0.000 0.000 0.007 4.004
1.002 0.151 0.002 1.837 0.000 0.000 0.007 4.002
0.989 0.145 0.002 1.854 0.000 0.000 0.007 3.989
1.004 0.150 0.002 1.835 0.001 0.001 0.007 3.999
0.995 0.144 0.002 1.850 0.000 0.000 0.007 3.995
1.001 0.146 0.002 1.840 0.001 0.001 0.008 4.001
FeO MnO MgO CaO Cr203
NiO Total Mg #
Formulae based on three cations
si Fe Mn Mg Ca Cr Ni O
1.004 0.168 0.003 1.815 0.001 0.001 0.007 4.001
1.003 0.143 0.002 1.843 0.000 0.000 0.008 4.003
liths (ave. 0.920; M a c K e n z i e and Canil, 1999) from the Slave province of the Canadian craton. This suggests that parts of the mantle root beneath the center of the Slave Province are slightly less refractory than the mantle underlying the cratonic margin beneath Somerset Island. The NiO contents of the olivine (ave. 0.38 wt.%) in both the lherzolites and harzburgites are, however, similar to those reported for the Slave craton (Jericho xenoliths ave. 0.39 wt.%, K o p y l o v a et al., 1999; Torrie xenoliths ave. 0.36 wt.%, M a c K e n z i e and Canil, 1999). 5.2.2. O r t h o p y r o x e n e
The M g # s of orthopyroxene in the peridotites range b e t w e e n 0.92 and 0.94 (ave. 0.930; Table 4), and are slightly higher than those of coexisting olivine suggesting equilibrated mineral parageneses (Gurney et al., 1979). The coarse and the porphyroclastic peridotites cannot be distinguished in terms of their orthopyroxene M g # s . Orthopyroxene in the pyroxenites exhibit a larger variation in M g # s , with an average value of 0.90 for high-Mg pyroxenites and 0.85 for l o w - M g pyroxenites. L o w A120 3 abun-
dances in both the peridotite and pyroxenite orthopyroxenes, ranging between 0.69 and 1.42 wt.%, reflect the presence of coexisting garnet.
5.2.3. C l i n o p y r o x e n e
The clinopyroxenes are chromium-rich diopsides (Table 5) and exhibit M g # s in the peridotites (ave. 0.929) that are similar to those of the coexisting orthopyroxene (Table 4). The M g # s of high-Mg pyroxenite clinopyroxene ( 0 . 9 2 - 0 . 9 4 ) overlap those of the clinopyroxene in the peridotites, whereas M g #s of l o w - M g pyroxenites (0.91) are considerably lower. The clinopyroxene C r 2 0 3 contents in the peridotites and the high-Mg pyroxenites range between 0.9 and 3.3 wt.% while the clinopyroxene of the l o w - M g pyroxenites exhibits lower C r 2 0 3 abundances (0.4 wt.%). The c h r o m i u m - d i o p s i d e s of the Nikos peridotites have slightly higher C r 2 0 3 contents than those reported for the Jericho ( 0 . 6 - 2 . 2 wt.%; Kopylova et al., 1999) and the Torrie xenoliths ( 0 . 3 - 1 . 5 wt.%; M a c K e n z i e and Canil, 1999) in the Slave province.
Table 4 Representative analyses of orthopyroxenes (analytical procedure as in Table 1) Sample Rock
NK1-5 Lherz
NK2-3 Lherz
NK2-10 Lherz
NK3-20 Lherz
N K 3 - 25 Lherz
NK1-2 Harz
NK1-3 Harz
NK1-6 Harz
NK1-7 Harz
NK1 - 17 Harz
NK1 - 18 Harz
NK2-7 Pyrox
NK3-1 Pyrox
NK3-17 Pyrox
SiO 2 TiO 2 A120 3 FeO MnO MgO CaO Na20 Cr20 3 NiO Total Mg #
56.69 0.09 1.22 5.00 0.13 35.00 0.71 0.14 0.49 0.10 99.59 0.926
56.66 0.08 0.96 4.58 0.11 35.97 0.23 0.04 0.27 0.09 99.00 0.933
56.78 0.06 1.04 5.01 0.11 35.27 0.34 0.09 0.35 0.11 99.18 0.926
57.04 0.00 1.01 4.95 0.12 35.35 0.53 0.01 0.29 0.07 99.37 0.927
56.79 0.09 1.24 5.34 0.12 34.78 0.68 0.13 0.35 0.10 99.64 0.921
57.11 0.04 0.95 4.72 0.12 35.80 0.34 0.09 0.38 0.08 99.63 0.931
57.18 0.05 0.97 4.65 0.13 35.89 0.30 0.08 0.34 0.08 99.69 0.932
56.35 0.04 1.14 4.53 0.11 35.82 0.38 0.15 0.47 0.10 99.09 0.934
56.50 0.06 1.35 4.57 0.11 35.62 0.83 0.15 0.56 0.09 99.84 0.933
56.56 0.01 0.90 4.46 0.12 36.18 0.34 0.09 0.33 0.07 99.06 0.935
56.34 0.03 1.20 4.48 0.11 35.18 0.72 0.13 0.61 0.12 98.95 0.933
57.02 0.06 0.95 4.97 0.11 35.70 0.22 0.03 0.18 0.08 99.34 0.928
56.16 0.03 1.11 9.68 0.14 32.66 0.20 0.01 0.18 0.15 100.34 0.857
55.64 0.02 1.17 9.66 0.12 32.55 0.22 0.00 0.17 0.15 99.72 0.857
1.961 0.002 0.043 0.145 0.003 1.816 0.013 0.006 0.010 0.003 5.984
1.962 0.002 0.040 0.165 0.003 1.810 0.008 0.001 0.006 0.002 5.989
1.956 0.002 0.050 0.154 0.004 1.787 0.025 0.009 0.010 0.003 5.983
1.959 0.001 0.038 0.135 0.003 1.831 0.012 0.006 0.010 0.002 5.980
1.960 0.001 0.039 0.133 0.004 1.834 0.011 0.005 0.009 0.002 5.981
1.940 0.001 0.046 0.130 0.003 1.839 0.014 0.010 0.013 0.003 5.966
1.934 0.002 0.054 0.131 0.003 1.818 0.030 0.010 0.015 0.002 5.965
1.946 0.000 0.037 0.128 0.003 1.856 0.012 0.006 0.009 0.002 5.965
1.948 0.001 0.049 0.130 0.003 1.814 0.027 0.009 0.017 0.003 5.976
1.963 0.002 0.039 0.143 0.003 1.832 0.008 0.002 0,005 0.002 5.984
1.955 0.001 0.045 0.282 0.004 1.695 0.008 0.000 0.005 0.004 5.979
1.948 0.001 0.048 0.283 0.004 1.699 0.008 0.000 0.005 0.004 5.975
Formulae based on f o u r cations Si 1.952 1.953 Ti 0.002 0.002 A1 0.049 0.039 Fe 0.144 0.132 Mn 0.004 0.003 Mg 1.797 1.849 Ca 0.026 0.008 Na 0.009 0.002 Cr 0.013 0.007 Ni 0.003 0.002 O 5.979 5.977
,..,~
4~
~t3
t,~
Table 5 Representative analyses of clinopyroxenes (analytical procedure as in Table 1) Sample Rock
NK1-5 Lherz
NK2-3 Lherz
NK2-10 Lherz
NK3-20 Lherz
NK3-25 Lherz
NK1-2 Harz
NK1-3 Harz
NK1-6 Harz
NK1-7 Harz
NKI-17 Harz
NKI-18 Harz
NK2-7 Pyrox
NK3-1 Pyrox
NK3-17 Pyrox
SiO 2 TiO 2 A120 3 FeO MnO MgO CaO Na20 Cr20 3 NiO Total Mg #
53.68 0.16 2.48 2.64 0.10 17.46 18.79 1.79 1.99 0.05 99.17 0.922
53.45 0.21 2.89 1.96 0.05 15.80 20.91 2.06 1.96 0.04 99.34 0.935
53.44 0.17 3.08 2.34 0.09 15.58 19.23 2.40 2.30 0.04 98.68 0.922
54.08 0.20 2.67 2.28 0.06 16.15 21.74 1.65 1.46 0.04 100.33 0.927
54.14 0.17 2.61 2.70 0.10 17.74 19.12 1.66 1.52 0.06 99.86 0.921
53.89 0.13 2.74 2.25 0.08 16.07 19.67 2.20 2.22 0.04 99.32 0.927
54.19 0.13 2.98 2.31 0.09 15.84 19.14 2.46 2.27 0.04 99.46 0.924
54.07 0.13 3.70 2.35 0.07 14.91 17.20 3.36 3.26 0.04 99.11 0.919
54.11 0.08 2.36 2.34 0.08 18.07 18.68 1.61 1.77 0.06 99.22 0.932
54.11 0.04 2.26 2.08 0.07 16.39 20.51 1.85 1.87 0.04 99.26 0.934
53.65 0.07 2.25 2.32 0.07 17.46 19.06 1.78 2.34 0.08 99.13 0.931
53.65 0.16 2.70 1.95 0.05 16.02 21.86 1.58 1.15 0.05 99.19 0.936
53.99 0.08 1.73 3.12 0.06 16.82 23.61 0.63 0.45 0.08 100.59 0.906
53.02 0.09 1.80 3.04 0.05 16.60 23.59 0.50 0.37 0.09 99.17 0.907
1.951 0.005 0.132 0.071 0.003 0.848 0.752 0.170 0.066 0.001 5.970
1.947 0.005 0.113 0.069 0.002 0.867 0.839 0.115 0.042 0.001 5.971
1.949 0.005 0.111 0.081 0.003 0.952 0.737 0.116 0.043 0.002 5.969
1.954 0.004 0.117 0.068 0.003 0.869 0.764 0.155 0.064 0.001 5.970
1.961 0.004 0.127 0.070 0.003 0.855 0.742 0.172 0.065 0.001 5.973
1.960 0.004 0.158 0.071 0.002 0.806 0.668 0.236 0.094 0.001 5.970
1.958 0.002 0.101 0.071 0.003 0.975 0.724 0.113 0.051 0.002 5.976
1.965 0.001 0.097 0.063 0.002 0.887 0.798 0.131 0.054 0.001 5.973
1.947 0.002 0.096 0.070 0.002 0.945 0.741 0.125 0.067 0.002 5.965
1.952 0.004 0.116 0.059 0.002 0.869 0.852 0.111 0.033 0.001 5.973
1.949 0.002 0.074 0.094 0.002 0.905 0.913 0.044 0.013 0.002 5.971
1.943 0.003 0.078 0.093 0.002 0.907 0.926 0.036 0.011 0.003 5.970
Formulae based on f o u r cations Si 1.947 1.936 Ti 0.004 0.005 A1 0.106 0.117 Fe 0.080 0.061 Mn 0.003 0.002 Mg 0.944 0.865 Ca 0.730 0.822 Na 0.126 0.137 Cr 0.057 0.053 Ni 0.001 0.001 O 5.967 5.961
g
4~ C~
I
t,,.)
Table 6 Representative analyses of garnets (analytical procedure as in Table 1) Sample Rock
NK1-5 Lherz
NK2-3 Lherz
NK2-1 0 Lherz
NK3-20 Lherz
NK3-25 Lherz
NK1-2 Harz
NK1-3 Harz
NK1-6 Harz
NK1-7 Harz
NKI-17 Harz
NKI-18 Harz
NK2-7 Pyrox
NK3-1 Pyrox
NK3-17 Pyrox
SiO 2 TiO 2 A120 3 FeO MnO MgO CaO Na 20 Cr20 3 NiO Total Mg #
41.35 0.25 18.92 6.89 0.38 20.52 5.11 0.03 4.78 0.01 98.22 0.842
41.34 0.08 21.44 7.85 0.48 19.53 5.28 0.03 3.21 0.01 99.27 0.816
41.42 0.09 21.27 7.57 0.41 20.01 5.07 0.03 3.74 0.02 99.63 0.825
42.01 0.07 22.56 9.38 0.46 19.03 4.80 0.01 1.92 0.01 100.27 0.783
41.84 0.32 20.76 7.23 0.33 20.11 5.02 0.03 3.71 0.01 99.38 0.832
41.91 0.09 20.04 7.15 0.45 20.48 5.05 0.02 3.99 0.00 99.18 0.836
41.65 0.09 19.70 7.27 0.48 20.23 5.22 0.02 4.29 0.00 98.97 0.832
41.51 0.08 20.58 6.86 0.38 20.66 4.62 0.03 4.42 0.01 99.16 0.843
41.46 0.14 20.29 6.24 0.30 20.67 5.22 0.02 4.76 0.02 99.12 0.855
41.38 0.02 20.78 7.01 0.42 19.88 5.45 0.04 4.12 0.01 99.14 0.835
41.05 0.13 18.51 6.36 0.32 19.79 5.94 0.02 6.77 0.02 98.92 0.847
41.67 0.04 23.35 8.11 0.48 20.11 4.65 0.01 1.49 0.00 99.93 0.815
40.67 0.05 22.00 14.89 0.60 14.63 5.88 0.01 1.32 0.00 100.05 0.637
40.53 0.09 22.49 14.88 0.56 14.97 6.07 0.01 1.27 0.00 100.89 0.642
Formulae based on eight cations Si 3.012 2.978 2.971 Ti 0.014 0.004 0.005 A1 1.624 1.821 1.798 Fe 0.419 0.473 0.454 Mn 0.023 0.029 0.025 Mg 2.228 2.098 2.140 Ca 0.399 0.408 0.390 Na 0.005 0.004 0.004 Cr 0.275 0.183 0.212 Ni 0.000 0.001 0.001 O 11.972 11.981 11.979
3.001 0.004 1.900 0.561 0.028 2.027 0.367 0.002 0.108 0.000 12.007
3.009 0.017 1.760 0.435 0.020 2.156 0.387 0.004 0.211 0.001 12.008
3.017 0.005 1.701 0.431 0.028 2.198 0.389 0.003 0.227 0.000 11.983
3.011 0.005 1.679 0.440 0.030 2.181 0.404 0.003 0.245 0.000 11.976
2.985 0.004 1.745 0.413 0.023 2.216 0.356 0.004 0.251 0.001 11.985
2.983 0.008 1.720 0.375 0.018 2.217 0.402 0.003 0.271 0.001 11.982
2.983 0.001 1.766 0.423 0.026 2.137 0.421 0.005 0.235 0.000 11.976
2.990 0.007 1.589 0.387 0.020 2.149 0.464 0.003 0.390 0.001 11.984
2.960 0.002 1.955 0.482 0.029 2.131 0.354 0.002 0.083 0.000 11.978
2.991 0.003 1.907 0.916 0.037 1.604 0.463 0.001 0.077 0.000 11.983
2.950 0.005 1.929 0.906 0.034 1.625 0.474 0.001 0.073 0.000 11.955
g ,..,.
,..,~ r~
r~ q~
I
t,,a
S.S. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
5.2.4. Garnet
The garnet in the peridotites and the high-Mg pyroxenites is a chromium-pyrope with high magnesium contents and Mges ranging between 0.79 and 0.86 (Table 6). Mges of garnet in the low-Mg pyroxenites are significantly lower (0.64). The garnets exhibit no chemical zoning and are homogeneous on the scale of a thin section. The pyrope-rich garnet of the Nikos xenoliths has high Cr203 contents ranging between 1.5 and 7.7 wt.%, with the highest values observed in the harzburgites (4.0-7.7 wt.%). CaO abundances in garnet are low and indistinguishable in peridotites and pyroxenites (4.5-6.4 wt.%). The garnets in the peridotites and high-Mg pyroxenites would be classified as Group 9 garnets in the statistical classification of garnets of Dawson and Stephens (1975), in agreement with previous results for garnets in peridotite xenoliths from other Somerset Island kimberlites (Kjarsgaard and Peterson, 1992). The garnets in the low-Mg pyroxenites
209
would be classified as Group 3 garnets because of their higher FeO and lower MgO contents. 5.3. Mineral modes
The modal mineral proportions of all Nikos xenoliths were calculated using a high-pressure peridotite norm calculation that determines the modal proportions of olivine, orthopyroxene, clinopyroxene, and garnet or spinel based on the whole rock compositions (Table 2). As a cross calibration, the normative mineralogy of twenty samples was calculated by reconstructing the bulk xenoliths from their mineral analyses using a least-squares technique. Both methods yield similar results, with modal mineral proportions differing by 3.0 _+ 1.8 wt.% (1 SD) for olivine, 3.0 ___2.5 wt.% (1 SD) for orthopyroxene, 1.3 _+ 0.6 wt.% (1 SD) for clinopyroxene, and 3.3 _+ 1.4 wt.% (1 SD) for garnet for all samples. The peridotite nodules range from garnet-lherzolites and garnet-
Fig. 6. Modal mineral proportions of Nikos xenoliths compared to data for kimberlite-hosted mantle xenoliths from the Kaapvaal craton in South Africa (Cox et al., 1973, 1987; Nixon and Boyd, 1973; Carswell et al., 1979; Danchin, 1979; Boyd and Mertzman, 1987). Primitive mantle composition after McDonough (1990).
S.S. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
210
harzburgites to garnet-dunites (average of all peridotites: olivine, 80 wt.%; orthopyroxene, 12 wt.%; chrome-diopside, 5 wt.%; pyrope-rich garnet, 3 wt.%). The majority of lherzolites fall rather close to the harzburgite field with only slightly more than 5 wt.% clinopyroxene (Fig. 6). These lherzolites exhibit major element compositions that are continuous with those of the harzburgites (Fig. 4a-c) and their division in two different rock types is somewhat artificial. The pyroxenites exhibit mineral assemblages consisting of clinopyroxene and orthopyroxene (ave. > 80 wt.%), and garnet (ave. 12 wt.%). The high-Mg pyroxenites contain 5-10 wt.% olivine, while the low-Mg pyroxenites contain no olivine. Traces of spinel and minor amounts of phlogopite (less than 1 vol.%) can be observed in individual xenolith samples.
5.4. Temperature and pressure
Temperatures and pressures of last equilibration were calculated for the Somerset xenoliths using geothermometers and barometers based on the compositions of coexisting pyroxenes and the solubility of A120 3 in orthopyroxene in the presence of garnet. Temperatures were determined using the thermometers of Finnerty and Boyd (1987) and Brey and KiShler (1990). That of Finnerty and Boyd (1987) uses an empirical data fit to the miscibility gap between coexisting orthopyroxene and clinopyroxene and has been cross calibrated with the diamond/graphite transition (Kennedy and Kennedy, 1976) and the phlogopite stability field at upper mantle conditions. The thermometer of Brey and KiShler (1990) is based on a thermodynamic model for the solubility
Table 7 Temperature and pressure estimates Sample
Rock
Texture
Two-PyroxBrey and KiShler (1990)
Al-in-Opx MacGregor (1974)
Two-Pyrox Finnerty and Boyd (1987)
MacGregor (1974)
Temperature ( ~
Pressure( k b )
Temperature (~
Pressure (kb)
54.5 42.5 18.3 26.6 40.8 51.7 51.1 31.0 22.6 23.1 53.9 49.2 44.7 46.1 33.9 48.8 54.8 48.0 45.3 63.8 48.4
1125 933 670 710 901 1124 1103 638 651 646 1121 1080 935 962 832 1029 1162 1058 980 1147 1022
46.3 36.7 20.7 23.4 34.5 44.9 44.2 19.5 16.1 17.5 45.5 44.0 37.7 39.3 31.1 41.8 46.9 43.5 40.6 55.9 41.6
43.2 52.0 56.1 23.8 44.3 23.2 18.4
926 1103 1067 606 949 -
38.1 45.2 47.7 17.0 38.9 -
NK1-5 NK 1- 14 NK1-23 NK2-3 NK2-10 NK3-4 NK3-15 NK3-20 NK3-22 NK3-24 NK3-25 NK 1-1 NK1-2 NK1-3 NK1-4 NK 1 - 6 NK1-7 NK1-9 NK1-12 NKI-13
Lherz Lherz Lherz Lherz Lherz Lherz Lherz Lherz Lherz Lherz Lherz Harz Harz Harz Harz Harz Harz Harz Harz Harz
coarse coarse coarse coarse coarse coarse coarse coarse porphyr coarse coarse coarse coarse coarse coarse coarse porphyr coarse coarse coarse
1261 1026 632 761 1001 1237 1218 819 762 738 1260 1186 1045 1070 878 1144 1293 1132 1054 1267
NKI-15 NK1-17 NK1-18 NK3-18 NK2-7 NK3-19 NK3-1 NK3-17
Harz Harz Harz Harz Pyrox Pyrox Pyrox Pyrox
coarse coarse coarse coarse coarse coarse coarse coarse
1132 1007 1215 1197 713 1033 739 657
Al-in-Opx
S.S. Schmidberger, D. Francis / Lithos 48 (1999) 195-216
of orthopyroxene in clinopyroxene and was calibrated in reversed experiments between 900 and 1400~ and 10 and 60 kb using natural fertile lherzolite compositions. These more recent experiments avoid Fe loss problems by using olivine crystals as sample containers. MacGregor (1974) showed that the solubility of A120 3 in orthopyroxene in the presence of garnet decreases with increasing pressure. Perkins and Newton (1980) used the same empirical method, but different thermodynamic parameters. The pressures calculated for the Nikos xenoliths using their calibration, however, were significantly lower than those obtained with the barometer of MacGregor (1974). The aluminum in enstatite (Al-in-en) barometer of MacGregor (1974) was evaluated by Finnerty and Boyd (1987) and found to yield results that are the most consistent with the diamond/graphite transition. The pressures and temperatures for the Nikos xenoliths (Table 7) are shown in Fig. 7. The method of Finnerty and Boyd (1987) combined with the Al-in-en barometer of MacGregor (1974) yields tem-
peratures and pressures (Table 7) that are on average about 100~ and 5 kb lower than the thermometer of Brey and K~Shler (1990). The calculated pressures and temperatures, however, define similar trends in P - T space for both thermometers. In the following discussion, only the results using the thermometer of Brey and K6hler (1990) will be used.
6. Discussion
6.1. Paleogeothermal regime The Nikos xenoliths record a wide range of equilibration conditions in the upper mantle, indicating that they were derived over a depth range between 55 and 170 km (Fig. 7). Although the pressure and temperature estimates for the harzburgites and lherzolites overlap, the harzburgites tend to plot at the higher end of the P - T array. This suggests that the upper part of the mantle sampled by the Nikos kimberlites tends to be more fertile than the lower portion of the mantle. A number of the peridotite
I
20
30
211
40
I
50
Pressure (kb) Fig. 7. Pressures and temperatures of last equilibration of the Nikos xenoliths using the thermometer of Brey and KiShler(1990) combined with the Al-in-en barometer of MacGregor (1974). Diamond/graphite transition after Kennedy and Kennedy (1976). Model conductive geotherms representing a surface heat flow of 40 and 44 mW/m 2 after Pollack and Chapman (1977). Data for peridotites from the Jericho kimberlite (Kopylova et al., 1999) in the Canadian Slave province, other xenolith data from the Nikos kimberlite on Somerset Island (Zhao et al., 1997) is shown for comparison.
212
S.S. Schmidberger, D. Francis/Lithos 48 (1999) 195-216
samples plot to the right of the diamond/graphite transition (Kennedy and Kennedy, 1976) and appear to have equilibrated within the diamond stability field. The pyroxenites yield the lowest pressures and temperatures, indicating that they may be derived from shallower depths. The calculated pressure and temperature data were fitted to a conductive geotherm using the approach of Pollack and Chapman (1977) assuming a lower crustal heat production of 0.25 ixW/m 3 for the Canadian shield and a heat production of 10 -2 ixW/m 3 for the underlying mantle. The paleogeotherm for the Nikos xenoliths corresponds to a surface heat flow of 44 m W / m 2 at the time of last equilibration in the mantle (Fig. 7). These results are similar to recently reported pressure and temperature results for other xenoliths from the Nikos kimberlite (Zhao et al., 1997; Fig. 7) and those reported for the Batty Bay kimberlite, located 35 km to the southwest on Somerset Island (Kjarsgaard and Peterson, 1992). Boyd and Canil (1997) report a conductive geotherm of 40 m W / m 2 for a peridotite suite from the Grizzly kimberlite pipe in the Slave province, consistent with pressure and temperature conditions obtained for peridotites from the Jurassic Jericho kimberlite in the Slave province (Fig. 7; Kopylova et al., 1999). These results suggest that the geothermal gradient is cooler beneath the center of the Slave craton than towards its margin beneath Somerset Island, or that the thermal conditions have changed from the Jurassic to the Cretaceous. The latter possibility is supported by the higher present day heat flow measurements at Yellowknife in the Slave province (51 mW/m2; Lewis and Wang, 1992) and at Resolute Bay in the Canadian Arctic (52 mW/m2; Lachenbruch, 1957). Above ~ l l00~ the pressure and temperature estimates for the Nikos peridotites deviate from the 44 m W / m 2 geotherm and are shifted towards slightly higher temperatures. This inflection is not correlated with any textural change in the xenoliths, as coarse peridotites are present at both the low and high temperature ends of the array. The inflection in the P - T array suggests the existence of a thermal boundary and may possibly represent the transition from lithospheric to asthenospheric mantle. This inflection would indicate a minimum thickness for the lithosphere of ~ 140 km beneath Somerset Island. The lithosphere boundary beneath the center of the
Slave province has been estimated to be at depths between 195 and 200 km on the basis of both seismic studies (Bostock, 1997) and xenolith evidence (Boyd and Canil, 1997). The 140-km depth of the inflection in the Nikos P - T array may suggest that the transition from the base of the lithosphere shallows from the center of the Slave craton to its margin beneath Somerset Island. This interpretation is consistent with results for the Kaapvaal craton, where the lithosphere-asthenosphere transition has been reported to shallow away from the cratonic center (200 km) to its margins ( ~ 140 km; Boyd, 1987). Porphyroclastic peridotites from the Kaapvaal craton in South Africa have been interpreted to represent asthenospheric mantle, whereas coarse peridotites are interpreted to represent lithospheric mantle (Boyd, 1987). Although a similar relationship apparently exists in the Jericho pipe of the Slave province (Kopylova et al., 1999), porphyroclastic xenoliths are rare in the Nikos pipe and do not give consistently higher P - T results. The lack of a correlation between texture and equilibration conditions observed for the Nikos peridotites is consistent with findings for the xenoliths from the Batty Bay kimberlite (Kjarsgaard and Peterson, 1992). 6.2. Nature of the Canadian mantle roots
Peridotite represents the dominant rock type ( > 90%) of the Nikos xenolith suite, indicating a peridotitic composition for Canadian mantle roots similar to that reported for the Kaapvaal and Siberian cratons (Nixon, 1987; Boyd et al., 1997). The chemical compositions of the Nikos peridotites are depleted in fusible elements compared to primitive mantle compositions (McDonough, 1990) and fertile spinel-lherzolites from beneath the Canadian Cordillera (Shi et al., 1998). The high olivine forsterite contents (ave. Fo = 92.3) and moderate to high modal abundances of olivine (ave. 80 wt.%) indicate the highly refractory nature of the Nikos peridotites and suggests that they represent the residues of large degree partial melting. The spectrum from lherzolite to harzburgite can be modeled using fractional melting equations based on Yb contents of the xenoliths. The results indicate an average of ~ 30% melt extraction from the most fertile lherzolite to refractory harzburgite.
213
S.S. Schmidberger, D. Francis/Lithos 48 (1999) 195-216
The chemical signatures of the Nikos peridotites are similar to the compositions reported for the Archean Kaapvaal and Siberian cratons (ave. olivine F o = 92.5; Boyd et al., 1997) and clearly distinct from the trend defined by peridotites from oceanic domains (ave. olivine Fo = 91.0; Boyd, 1989) and spinel-peridotites from the Canadian Cordillera (Shi et al., 1998) that represent the mantle beneath Phanerozoic accreted terranes along the western margin of the Canadian shield (Fig. 8). Spinel-harzburgites associated with a mantle thermal anomaly beneath the southwestern Yukon (Shi et al., 1998), however, have intermediate compositions with higher modal olivine and olivine forsterite contents compared to the more fertile spinel-lherzolites, and trend towards the more depleted compositions of the Nikos peridotites. These spinel-harzburgites were interpreted to represent the residue of ~ 20-25% partial melting of lherzolite mantle (Francis, 1987; Shi et al., 1998). Many peridotite xenoliths from the Kaapvaal craton are anomalously enriched in orthopyroxene, with average modal orthopyroxene contents of 32 wt.% (Boyd et al., 1997). Minor occurrences of such orthopyroxene-rich mineral assemblages have been re-
ported from the Siberian craton (Boyd et al., 1997), however, these peridotites have an average orthopyroxene content of only 20 wt.% and are thus less enriched in orthopyroxene than the Kaapvaal xenoliths. This orthopyroxene-rich nature cannot be attributed solely to the extraction of basaltic components from primitive mantle by extensive partial melting (Herzberg, 1993). Such processes would induce depletion in both clinopyroxene and orthopyroxene content, and a shift of the residual mineral assemblage to higher olivine, but lower orthopyroxene abundances. A recent experimental study on depleted cratonic harzburgite by Kinzler and Grove (1998), however, has shown that the majority of the orthopyroxene enriched mineral assemblages from the Kaapvaal and Siberian cratons can be produced by polybaric, near fractional melting of primitive mantle at > 2 GPa. The most extreme orthopyroxene enriched peridotites, however, cannot be explained by such processes and these require that either parts of the mantle are significantly enriched in silica compared to primitive mantle models (Herzberg, 1993) or that post melt-extraction processes have modified the composition of the Kaapvaal mantle roots (e.g., Boyd et al., 1997; Kelemen et al.,
9 -
o
o
/
/
"
,,.
AA,
AO
'",.,,o o -
9 A
.....
AA
g.
9
xZ
o
~r
o
(23
Fig. 8. Modal olivine content (wt.%) vs. Mg # in olivine of the Nikos peridotites. Field for the Kaapvaal and Siberian cratons (Boyd, 1989; Boyd et al., 1997) and data for the Canadian Cordillera (Shi et al., 1998" lherzolites, open circles; harzburgites, open triangles) are shown for comparison. Trend defined by oceanic peridotites after Boyd (1989).
214
S.S. Schmidberger, D. Francis /Lithos 48 (1999) 195-216
1997). Igneous separation of orthopyroxene-rich cumulate layers or metamorphic segregation of the residual mantle into orthopyroxene- and olivine-rich layers have been proposed by Boyd et al. (1997) as possible explanations for the orthopyroxene-rich nature of cratonic mantle roots. Such processes would induce a negative correlation between Si and Fe, opposite to the trend observed in melting experiments on fertile garnet-peridotite (Hirose and Kushiro, 1993; Baker and Stolper, 1994). In the Nikos xenolith suite, however, a negative correlation between Si and Fe (Fig. 9), that has been reported for Siberian and Kaapvaal peridotites (Boyd et al., 1997), is not observed. Kelemen et al. (1997) interpreted a positive correlation between NiO in olivine and modal orthopyroxene contents in some cratonic mantle xenolith suites to be indicative of metasomatic infiltration of residual mantle by Fe-poor silicic melts, possibly originating from subducted oceanic lithosphere. This would induce the formation of orthopyroxene at the expense of olivine, resulting in increased NiO in the residual olivine associated with high orthopyroxene abundances. This trend between modal orthopyroxene and olivine NiO contents is not well developed in the Nikos peridotites (Fig. 10). Compared to xenolith suites from the Kaapvaal and Siberian cratons, the Nikos peridotites are characterized by lower orthopyroxene abundances (ave. 12 wt.%). The chemical and modal signatures of the Nikos peridotites are similar to those recently re-
0.44 (19
Harzburgite
c-
"7 o . m m
0.42
Fig. 10. NiO (wt.%) in olivine vs. modal orthopyroxene content (wt.%) of the Nikos peridotites.
ported for the Grizzly kimberlite peridotites in the Slave province (Boyd and Canil, 1997), which also have high magnesium numbers (ave. Mg # = 0.927), but mineral assemblages characterized by relatively low orthopyroxene (ave. ~ 11 wt.%; MacKenzie and Canil, 1999). The trend towards higher olivine and lower orthopyroxene abundances exhibited by the Nikos peridotites suggests an origin by large degree partial melting of primitive mantle compositions. This interpretation is supported by continuous trends in major element variations, in particular the negative correlation of MgO and A120 3 (Fig. 4a), suggesting that the Nikos peridotites are related by partial melting. It is also consistent with an overall positive correlation between modal olivine abundance and olivine forsterite content (Fig. 8).
7. Conclusions
9 LL
6
~149
~
5
Fig. 9. Variation of FeO and SiO 2 (wt.%) of the Nikos peridotites indicating no correlation of these elements in the xenoliths.
The Nikos peridotites define a hotter paleogeotherm than that reported for the mantle beneath the central Slave province. An inflection in the pressure and temperature array may indicate that the transition from lithospheric to asthenospheric mantle is shallower under Somerset Island (140 km) than under the center of the Slave craton (200 km). The high forsterite contents associated with moderate to high olivine abundances of the Nikos peridotites are characteristic of peridotite xenolith suites derived from subcontinental mantle beneath Archean cratons. These characteristics clearly indicate that
S.S. Schmidberger, D. Francis /Lithos 48 (1999) 195-216
they are distinctly more refractory than oceanic peridotites and post-Archean mantle xenolith suites. The modal abundances of the Nikos xenoliths suggest that they formed by extensive degrees of partial melting of primitive mantle. However, the high orthopyroxene abundances that characterize the Kaapvaal craton and parts of the Siberian craton are not characteristic of the Nikos peridotite suite. More studies of mantle xenolith suites from other Archean cratons are needed to determine whether the orthopyroxene-rich mantle roots beneath the Kaapvaal craton are an exception, or a general feature of cratonic mantle roots.
Acknowledgements We would like to thank Tariq Ahmedali for performing the bulk rock X-ray fluorescence analyses and Glenn Poirier for his help in obtaining the electron microprobe results. We also thank Fabien Rasselet for assistance in the field, hand picking separates of magmatic kimberlite for major and trace element analysis, and performing the CO 2 analyses with the assistance of Constance Guignard. Tony Simonetti is thanked for discussions and earlier revisions of the manuscript.
References Baker, M.B., Stolper, E.M., 1994. Determining the composition of high-pressure mantle melts using diamond aggregates. Geochim. Cosmochim. Acta 58, 2811-2827. Bostock, M.G., 1997. Anisotropic upper-mantle stratigraphy and architecture of the Slave craton. Nature 390, 392-395. Boyd, F.R., 1987. High- and low-temperature garnet peridotite xenoliths and their possible relation to the lithosphereasthenosphere boundary beneath southern Africa. In: Nixon, P.H. (Ed.), Mantle Xenoliths. Wiley, Chichester, pp. 403-412. Boyd, F.R., 1989. Compositional distinction between oceanic and cratonic lithosphere. Earth Planet. Sci. Lett. 96, 15-26. Boyd, F.R., Canil, D., 1997. Peridotite xenoliths from the Slave craton, Northwest Territories. Seventh Annual V.M. Goldschmidt Conference, Houston, 34-35. Boyd, F.R., Mertzman, S.A., 1987. Composition and structure of the Kaapvaal lithosphere, southern Africa. In: Mysen, B.O. (Ed.), Magmatic Processes: Physiochemical Principles. Geochem. Soc. Spec. Publ., pp. 13-24. Boyd, F.R., Pokhilenko, N.P., Pearson, D.G., Mertzman, S.A., Sobolev, N.V., Finger, L.W., 1997. Composition of the Siberian cratonic mantle: evidence from Udachnaya peridotite xenoliths. Contrib. Mineral. Petrol. 128, 228-246.
215
Brey, G.P., Ktihler, T., 1990. Geothermobarometry in four-phase lherzolites: II. New thermobarometers, and practical assessment of existing thermobarometers. J. Petrol. 31, 1353-1378. Carswell, D.A., Clarke, D.B., Mitchell, R.H., 1979. The petrology and geochemistry of ultramafic nodules from Pipe 200, northern Lesotho. In: Boyd, F.R., Meyer, H.O.A. (Eds.), Proceedings of the Second International Kimberlite Conference. AGU, Washington, pp. 127-144. Cox, K.G., Gurney, J.J., Harte, B., 1973. Xenoliths from the Matsoku pipe. In: Nixon, P.H. (Ed.), Lesotho Kimberlite. Lesotho National Development, Maseru, Lesotho, pp. 76-100. Cox, K.G., Smith, M.R., Beswetherick, S., 1987. Textural studies of garnet lherzolites: evidence of exsolution origin from hightemperature harzburgites. In: Nixon, P.H. (Ed.), Mantle Xenoliths. Wiley, Chichester, pp. 537-550. Dalton, J.A., Presnall, D.C., 1997. Phase relations in the system C a O - M g O - A I 2 0 3 - S i O 2-CO 2 from 3.0 to 7.0 GPa: carbonatites, kimberlites and carbonatite-kimberlite relations. GAC/MAC Annual Meeting, Ottawa, A-34. Danchin, F.R., 1979. Mineral and bulk chemistry of garnet lherzolite and garnet harzburgite from the Premier mine, South Africa. In: Boyd, F.R., Meyer, H.O.A. (Eds.), Proceedings of the Second International Kimberlite Conference. AGU, Washington, pp. 104-126. Dawson, J.B., 1980. Kimberlites and their xenoliths. SpringerVerlag, Berlin, 252 pp. Dawson, J.B., Stephens, W.E., 1975. Statistical classification of garnets from kimberlite and associated xenoliths. J. Geol. 83, 589-607. Finnerty, A.A., Boyd, F.R., 1987. Thermobarometry for garnet peridotites: basis for the determination of thermal and compositional structure of the upper mantle. In: Nixon, P.H. (Ed.), Mantle Xenoliths. Wiley, Chichester, pp. 381-402. Francis, D., 1987. Mantle-melt interaction recorded in spinel lherzolite xenoliths from the Alligator Lake volcanic complex, Yukon, Canada. J. Petrol. 28, 569-597. Frisch, T., Hunt, P.A., 1993. Reconnaissance U-Pb geochronology of the crystalline core of the Boothia Uplift, District of Franklin, Northwest Territories. Radiogenic Age and Isotope Studies: Report 7. Geological Survey of Canada, Paper, pp. 3-22. Grand, S.P., 1994. Mantle shear structure beneath the Americas and surrounding oceans. J. Geophys. Res. 99, 11591-11621. Gurney, J.J., Harris, J.W., Rickard, R.S., 1979. Silicate and oxide inclusions in diamonds from the Finsch kimberlite pipe. In: Boyd, F.R., Meyer, H.O.A. (Eds.), Kimberlites, Diatremes and Diamonds: Their Geology and Petrology and Geochemistry. AGU, Washington, pp. 1- 15. Harte, B., 1977. Rock nomenclature with particular relation to deformation and recrystallization textures in olivine-bearing xenoliths. J. Geol. 85, 279-288. Hatton, C.J., Gurney, J.J., 1987. Roberts Victor eclogites and their relation to the mantle. In: Nixon, P.H. (Ed.), Mantle Xenoliths. Wiley, Chichester, pp. 453-463. Heaman, L.H., 1989. The nature of the subcontinental mantle from Sr-Nd-Pb isotopic studies on kimberlite perovskite. Earth Planet. Sci. Lett. 92, 323-334.
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Herzberg, C.T., 1993. Lithosphere peridotites of the Kaapvaal craton. Earth Planet. Sci. Lett. 120, 13-29. Hirose, K., Kushiro, I., 1993. Partial melting of dry peridotites at high pressures: determination of compositions of melts segregated from peridotite using aggregates of diamond. Earth Planet. Sci. Lett. 114, 477-489. Jago, B.C., Mitchell, R.H., 1987. Ultrabasic xenoliths from the Ham kimberlite, Somerset Island, Northwest Territories. Can. Miner. 25, 515-525. Jordan, T.H., 1988. Structure and formation of the continental tectosphere. J. Petrol., Spec. Lithosphere Issue, 11-37. Kelemen, P.B., Bernstein, S., Hart, S.R., 1997. SiO 2 addition to cratonic mantle via melt/rock reaction above subduction zones. Workshop on Continental Roots. Harvard University and MIT. Kennedy, C.S., Kennedy, G.C., 1976. The equilibrium boundary between graphite and diamond. J. Geophys. Res. 81, 24672470. Kinzler, R.J., Grove, T.L., 1998. Origin of depleted cratonic harzburgite by deep fractional melt extraction and shallow olivine cumulate infusion. Proceedings of the Seventh International Kimberlite Conference, in press. Kjarsgaard, B.A., Peterson, T.D., 1992. Kimberlite-derived ultramafic xenoliths from the diamond stability field: a new Cretaceous geotherm for Somerset Island, Northwest Territories. Current Research, 1992-B. Geological Survey of Canada, pp. 1-6. Kopylova, M.G., Russell, J.K., Cookenboo, H., 1999. Petrology of peridotite and pyroxenite xenoliths from the Jericho kimberlite: implications for the thermal state of the mantle beneath the Slave craton, Northern Canada. J. Petrol. 40, 79-104. Lachenbruch, A.H., 1957. Thermal effects of the ocean on permafrost. Geol. Soc. Am. Bull. 68, 1515-1529. Lewis, T.J., Wang, K., 1992. Influence of terrain on bedrock temperatures. Palaeogeogr., Palaeoclimatol., Palaeoecol. 98, 87-100. MacGregor, I.D., 1974. The system MgO-AI203-SiO2: solubility of A120 3 in enstatite for spinel and garnet peridotite compositions. Am. Mineral. 59, 110-119. MacKenzie, J.M., Canil, D., 1999. Composition and thermal evolution of cratonic mantle beneath the central Archean Slave Province, NWT, Canada. Contrib. Mineral. Petrol. 134, 313324. McDonough, W.F., 1990. Constraints on the composition of the continental lithospheric mantle. Earth Planet. Sci. Lett. 101, 1-18. Mitchell, R.H., 1975. Geology, magnetic expression, and structural control of the central Somerset Island kimberlites. Can. J. Earth Sci. 12, 757-764. Mitchell, R.H., 1977. Ultramafic xenoliths from the Elwin Bay kimberlite: the first Canadian paleogeotherm. Can. J. Earth Sci. 14, 1202-1210. Mitchell, R.H., 1978. Mineralogy of the Elwin Bay kimberlite, Somerset Island, NWT, Canada. Am. Mineral. 63, 47-57. Mitchell, R.H., 1986. Kimberlites: Mineralogy, Geochemistry, and Petrology. Plenum, New York, 442 pp. Mitchell, R.H., Meyer, H.O.A., 1980. Mineralogy of micaceous
kimberlite from the Jos dyke, Somerset Island. Can. Mineral. 18, 241-250. Nixon, P.H., 1987. Kimberlitic xenoliths and their cratonic setting. In: Nixon, P.H. (Ed.), Mantle Xenoliths. Wiley, Chichester, pp. 215-239. Nixon, P.H., Boyd, F.R., 1973. Petrogenesis of the granular and sheared ultrabasic nodule suite in kimberlites. In: Nixon, P.H. (Ed.), Lesotho Kimberlites. Lesotho National Development, Maseru, Lesotho, pp. 48-56. Nixon, P.H., Rogers, N.W., Gibson, I.L., Grey, A., 1981. Depleted and fertile mantle xenoliths from southern African kimberlites. Annu. Rev. Earth Planet. Sci. 9, 285-309. Okulitch, A.V., Trettin, H.P., 1991. Late Cretaceous - - Early Tertiary deformation, Artic Islands. In: Trettin, H.P. (Ed.), Geology of the Innuitian Orogen and Artic Platform of Canada and Greenland. Geological Survey of Canada, pp. 469-489. Pell, J., 1993. New kimberlite discoveries on Somerset Island. Exploration Overview 1993. NWT Geology Division, Department of Indian and Northern Affairs, Yellowknife, 47 pp. Perkins, D., Newton, R.C., 1980. The compositions of coexisting pyroxenes and garnet in the system CaO-MgO-A1203-SiO 2 at 900~176 and high pressures. Contrib. Mineral. Petrol. 75, 291-300. Pollack, H.N., Chapman, D.S., 1977. On the regional variation of heat flow, geotherms and lithospheric thickness. Tectonophysics 38, 279-296. Ringwood, A.E., Kesson, S.E., Hibberson, W., Ware, N., 1992. Origin of kimberlites and related magmas. Earth Planet. Sci. Lett. 113, 521-538. Shi, L., Francis, D., Ludden, J., Frederiksen, A., Bostock, M., 1998. Xenolith evidence of lithospheric melting above anomalously hot upper mantle under the northern Canadian Cordillera. Contrib. Mineral. Petrol. 131, 39-53. Smith, C.B., Allsopp, H.L., Garvie, O.G., Kramers, J.D., Jackson, P.F.S., Clement, C.R., 1989. Note on the U-Pb perovskite method for dating kimberlites: examples from the Wesselton and DeBeers mines, South Africa, and Somerset Island, Canada. Chem. Geol. (Isotope Geos.) 79, 137-145. Steward, W.D., 1987. Late Proterozoic to Early Tertiary stratigraphy of Somerset Island and northern Boothia Peninsula, District of Franklin. Geological Survey of Canada Papers, 83-26, 78 pp. Trettin, H.P., Frisch, T.O., Sobczak, L.W., Weber, J.R., Niblett, E.R., Law, L.K., DeLaurier, I., Witham, K., 1972. The Innuitian Province. In: Price, R.A., Douglas, R.J.W. (Eds.), Variations in Tectonic Styles in Canada. Geological Association of Canada, Special Paper, pp. 83-179. Woolley, A.R., Kempe, D.R.C., 1989. Carbonatites nomenclature, average chemical compositions, and elemental distribution. In: Bell, K. (Ed.), Carbonatites: Genesis and Evolution. Unwin Hyman, London, pp. 1-14. Zhao, D., Essene, E.J., Zhang, Y., Hall, C.M., Wang, L., 1997. Newly discovered kimberlites and mantle xenoliths from Somerset Island and Brodeur Peninsula, Canada: pressure, temperature, oxygen fugacity, volatile content and age. NWT Geology Division, Department of Indian and Northern Affairs, Yellowknife, pp. 1-105.
LITHOS
ELSEVIER
Lithos 48 (1999) 217-235
0
Evidence from mantle xenoliths for relatively thin (< 100 km) continental lithosphere below the Phanerozoic crust of southernmost South America Charles R. Stern a,,, Rolf Kilian b,1 Bettina Olker T. Kurtis Kyser e,4
c,2
Eric H. Hauri 6,3
Department of Geological Sciences, University of Colorado, Boulder, CO 80309-0399, USA b Geologisches Institut, Universitiit Freiburg, D-79104 Freiburg, Germany c Mineralogisches Institut, Universit~t Heidelberg, 69120 Heidelberg, Germany d Department of Terrestrial Magnetism, Carnegie Institution of Washington, Washington, DC 20015, USA e Department of Geological Sciences, Queen's University, Kingston, Ontario, Canada K7L 3N6 a
Received 6 April 1998; received in revised form 8 February 1999; accepted 9 February 1999
Abstract
Garnet peridotite xenoliths in the Quaternary Pali-Aike alkali olivine basalts of southernmost South America are samples of the deeper portion of continental lithosphere formed by accretion along the western margin of Gondwanaland during the Phanerozoic. Core compositions of minerals in garnet peridotites indicate temperatures of 970 to 1160~ between 1.9 and 2.4 GPa, constraining a geothermal gradient which suggests a lithospheric thickness of approximately 100 km below this region. Previously, this lithosphere may have been heated and thinned to < 80 km during the Jurassic break-up of Gondwanaland, when widespread mafic and silicic volcanism occurred in association with extension in southern South America. Subsequent cooling, by up to > 175~ and thickening, by about 20 km, of the lithosphere is reflected in low-temperature ( < 970~ spinel peridotites by chemical zonation of pyroxenes involving a rimward decrease in Ca, and in moderate- and high-temperature ( > 970~ peridotites by textural evidence for the transformation of spinel to garnet. A recent heating event, which probably occurred in conjunction with modal metasomatism related to the genesis of the Pali-Aike alkali olivine basalts, has again thinned the lithosphere to < 100 km. Evidence for this heating is preserved in moderate- and high-temperature ( > 970~ peridotites as chemical zonation of pyroxenes involving a rimward increase in Ca, and by kelyphitic rims around garnet. The majority of moderate- and high-temperature ( > 970~ xenoliths are petrochemically similar to the asthenospheric source of mid-oceanic ridge basalts: fertile ( > 20% modal clinopyroxene and garnet), Fe-rich garnet lherzolite with major element composition similar to estimates of primitive mantle, but large-ion-lithophile and light-rare-earth element depletion relative to heavy-rare-earth elements, and with Sr, Nd, Pb, Os, and O isotopic compositions similar to MORB. In contrast, infertile, Mg-rich spinel harzburgite is predominant among low-temperature ( < 970~ xenoliths. This implies a significant chemical gradient and increasing density with depth in the mantle section
* Corresponding author. Fax: + 1-303-492-2606; E-mail: [email protected] 1 Fax: + 49-0761-2036496; E-mail: [email protected]. 2 Fax: + 49-6221-544805; E-mail: [email protected]. 3 Fax: + 1-202-364-8726; E-mail: [email protected]. 4 Fax: + 1-613-533-6592; E-mail: [email protected]. 0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All fights reserved. PII: S0024-4937(99)00030-4
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C.R. Stern et al./Lithos 48 (1999) 217-235
represented by the xenoliths, and the absence of a deep, low density, olivine-rich root below the southernmost South American crust such as has been inferred below Archean cratons. With respect to both temperature/rheology and chemistry/density, the subcontinental mantle lithosphere below southernmost South America is similar to that below oceanic crust. It is interpreted to have formed by tectonic capture, during the Paleozoic, of a segment of what had previously been oceanic lithosphere generated at a late Proterozoic mid-oceanic spreading ridge. 9 1999 Elsevier Science B.V. All rights reserved. Keywords: Mantle; Lithosphere; Peridotite; Xenolith; South America
1. Introduction Garnet peridotite xenoliths from the Quaternary Pali-Aike alkali olivine basalt field, southernmost South America (Fig. 1), provide a unique window into the deeper portions of subcontinental lithosphere in a region where crustal rocks are Phanerozoic in
r ~,~ I
age (de Wit, 1977; Ramos, 1988). Based on mineral thermometry and barometry, Skewes and Stern (1979), Stern et al. (1986, 1989), and Douglas et al. (1987) concluded that the subcontinental mantle lithosphere below this region has a high geothermal gradient of > 1 0 ~ between 50 and 100 km depth, with temperature of > 1300~ at depths of
Argentina
I
Cenozoic basalts
)O
Fig. 1. Map of southern South America showing the location of the Quaternary Pali-Aike (PA) alkali olivine basalt field, from which the xenoliths discussed in this paper were obtained, and other late Cenozoic basalts of the Patagonian plateau lavas (Stern et al., 1986, 1989, 1990). Also shown are tectonic features such as plates, plate boundaries (Cande and Leslie, 1986), and the adakitic stratovolcanoes of the Andean Austral Volcanic Zone (AVZ; Stern and Kilian, 1996).
219
C.R. Stern et al./Lithos 48 (1999) 217-235
< 100 km (Fig. 2), suggesting the lack of a deep subcontinental lithospheric root below this region of southernmost South America. Xenoliths in the Pali-Aike basalts are dominantly harzburgites and lherzolites, along with minor websterites and pyroxenites. Stern et al. (1986, 1989) demonstrated that with increasing depth in the subcontinental lithosphere below southernmost South America, the proportion of denser, more fertile lher-
zolite increases relative to less dense, less fertile harzburgite. They concluded that the deepest portion of this subcontinental lithosphere consists of fertile garnet lherzolite with major element composition similar to "pyrolite" and trace-element and isotopic characteristics similar to the global asthenospheric mantle source of mid-ocean ridge basalts. Thus with respect to both temperature/rheology and chemistry/density, the subcontinental mantle
0
g
Fig. 2. Estimates of the temperature and pressure of equilibration of Pali-Aike garnet peridotites (open symbols) based on the Ca-in-orthopyroxene thermometer and Al-in-orthopyroxene barometer of Brey and K~hler (1990) as applied to mineral core compositions (Olker, 1997). For the spinel websterite Pa2, pressure was estimated based on the Ca-in-olivine barometer and temperature estimated with the two-pyroxene thermometer of Brey and KiShler (1990). These T and P estimates plot close to the 65-roW m-1 geotherm of Chapman (1986), and the geotherm they define (dashed line) intersects the adiabatic upwelling curve (AAC) of McKenzie and Bickle (1988) at about 100 km, implying a thin lithosphere below Pali-Aike. This geotherm is similar to a previous one (solid symbols; Stern et al., 1989) based on independent microprobe mineral composition data and calculated with a different two-pyroxene thermometer (Wells, 1977) and the garnet-orthopyroxene barometer (Nickel and Green, 1985). As discussed in the text, the base of the lithosphere below Pali-Aike has recently been heated to higher temperatures than those implied by core compositions of xenolith minerals, and thinned to < 100 km (see Fig. 9).
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C.R. Stern et al. / Lithos 48 (1999) 217-235
Fig. 3. Photomicrographs of three garnet peridotites from Pali-Aike. Garnet lherzolite LS33, which is the highest temperature (1160 to 1220~ Figs. 2 and 4) xenolith documented, has a weakly porphyroclastic, but unfoliated texture. Moderate-temperature (990~ Fig. 2) spinel + garnet lherzolite BN4 also has equigranular texture. The spinel + garnet harzburgite TM 15 is cut by a high-Ti phlogopite vein. The photomicrographs of LS33 and BN4 are both 3 cm across, while that of TM15 is 4 cm across. Minerals are O1 = Mg-olivines (clear), Opx = Mg-orthopyroxenes (grey, olive green in thin section), Cpx = Cr-diopside clinopyroxene (grey, emerald green in thin section), Gt = pyrope garnets (grey, reddish in thin section), Phi = phlogopite (dark brown to reddish brown in thin section due to their high-Ti content), and Sp = spinels (opaque).
C.R. Stern et al./Lithos 48 (1999) 217-235
221
Fig. 3 (continued).
lithosphere below southernmost South America is apparently similar to that below oceanic crust and distinctly different from that below Archean cratons. This paper presents the results of new electron and ion microprobe determinations of mineral chemistry and new Sr, Nd, Pb, Os and O isotopic data that substantiate the conclusion that not all continental crust is underlain by a thick (>> 100 km) lithospheric mantle root.
2. Xenolith petrochemistry 2.1. Xenolith mineralogy and lithology Xenoliths in the Pali-Aike basalts include sedimentary and granitic rocks, mafic and silicic metaigneous granulites (Selverstone and Stern, 1983), pyroxenites, olivine websterites, and mantle-derived Type I Cr-diopside peridotites (Skewes and Stern, 1979; Stern et al., 1986, 1989). Eclogites are scarce. Secondary effects such as melt infiltration or grain boundary melting related to heating, decompression
and reaction with the basaltic host during transport to the surface are either minimal or absent in most peridotite xenoliths, as is weathering or serpentinization. The peridotites generally have coarse equigranular textures (Fig. 3), and are not strongly foliated (Douglas et al., 1987). Peridotites include spinel, spinel + garnet, and garnet harzburgites and lherzolites consisting dominantly of Mg-olivine (Fo85-92), orthopyroxene (En82-90), Cr-diopside clinopyroxene, Cr-pyrope garnet and spinel, as well as minor pargasitic amphibole and Ti-phlogopite mica which occur both in veins (sample TM15 in Fig. 3) and as isolated mineral grains. Representative electron microprobe analysis of mineral major-element chemistry in Pali-Aike peridotite xenoliths have been presented in the works of Skewes and Stern (1979), Douglas et al. (1987) and Stern et al. (1989). Spinels include both highA1/low-Cr types, which occur exclusively in lowtemperature ( < 970~ garnet-free peridotites, and also low-A1/high-Cr types, which occur in moderate- and high-temperature ( > 970~ peridotites (Stem et al., 1986). Spinel in garnet + spinel xenoliths is always the low-A1/high-Cr type and is typi-
222
C.R. Stern et al./Lithos 48 (1999) 217-235
cally fully enclosed as inclusions in garnet (samples BN4 and TM15 in Fig. 3). These spinels are interpreted as relics of the reaction spinel + pyroxene garnet + olivine. Also, garnet in peridotites without spinel often have inclusions of olivine, suggesting that they formed by the same reaction from originally spinel-bearing peridotites. This reaction may result from either cooling, pressure increase, or both, indicating a multi-stage thermal history for the lithosphere below Pali-Aike, as discussed in more detail below. Exsolution of clinopyroxene from orthopyroxene, and vice versa, in some low-temperature ( < 970~ spinel peridotites and olivine websterites, is also considered to be mineralogic evidence for cooling. In contrast, garnets in relatively high-temperature ( > 970~ garnet peridotites have kelyphitic rims containing pyroxenes and spinel, suggesting an increase in temperature. New electron microprobe analysis, which involved systematic rim-to-core-to-rim profiles of olivines, pyroxenes, spinels and garnets, indicate that core compositions of minerals are consistent with previously published analyses, but that different xenoliths have distinctive core-to-rim chemical zonations. These zonations involve the elements A1 and Ca (Fig. 4), but not Fe or Mg, possibly due to the more rapid diffusion rates of these latter elements
Fig. 4. Rim-to-rim zonations in Ca (circles) and A1 (squares) concentrations (pfu = per formula unit) across orthopyroxene grains in spinel and garnet peridotites as determined by electron microprobe profiles. Core and rim temperatures were calculated by applying both the Ca-in-orthopyroxene and two-pyroxene thermometers of Brey and KiShler (1990); the former listed to the left of the slash, the latter to the right. Based on analysis of multiple pairs of grains, errors in the calculated temperatures are estimated as _+20~ for the cores (which may or may not be true cores) and __+12~ for the rims. As discussed in the text, the two-pyroxene thermometer is considered to more closely approach final equilibration temperature since Mg exchange between orthopyroxene and clinopyroxene is more rapid than Ca diffusion in orthopyroxene. For the low-T spinel peridotite LS2, the rim indicates a lower temperature than the core as estimated by the Ca-in-orthopyroxene thermometer, and the two-pyroxene thermometer gives a significantly lower temperature, because Ca diffusion slowed during progressive cooling. For the high-T garnet-bearing xenoliths, the rim indicates higher temperature than the core and the two-pyroxene thermometer gives higher temperatures because Ca diffusion has not kept pace with Mg exchange between the two pyroxenes during heating.
(Sautter and Harte, 1988; Witt-Eickschen and Seck, 1991; Werling and Altherr, 1997). Furthermore, A1 and Ca zonations are much more pronounced in orthopyroxene than in clinopyroxene, reflecting differences in the diffusion rates of these cations between both pyroxene types (Werling and Altherr, 1997). Some spinel peridotites and olivine websterites, those that equilibrated at relatively low temperatures ( < 970~ have orthopyroxenes characterized by broad homogeneous cores and decreasing A1 and Ca contents across the rims (LS-2; Fig. 4). In contrast, orthopyroxenes from high-temperature ( > 970~ spinel and garnet peridotites have increasing A1 and Ca contents from their cores to their rims, but this zoning pattern is parabolic, and these grains do
o~~
Table 1 Compositions of Pali-Aike peridotites, published estimates of Primitive Mantle, and averages of other spinel and garnet peridotites (Hofm = Hofmann (1988); All~gre = All~gre et al. (1995); P&M = Palme and Nickel (1985); Ringw = Ringwood (1979); McDon = McDonough (1990); SpP-1 and SpP-2 = Average continental spinel peridotites (MaalCe and Aoki, 1975; McDonough, 1990); GtP-1 = Average continental garnet peridotites (M&A = MaalCe and Aoki, 1975); Lherz = Average Pali-Aike (PA) garnet-bearing lherzolite; Stern = determined by wet chemical analysis (Stern et al., 1989); Olker (1997) and Kilian = independent X R F determinations using standards JP-6 and SARM47, Heidelberg University) Estimates of the Primitive Mantle
SiO 2 TiO 2 A120 3 FeOto t MnO MgO CaO Na20 K20 Cr20 3 NiO Sum Mg#
Peridotite averages
Spinel-garnet harzburgites
Hofm
All~gre
P&M
Ringw
McDon
SpP- 1
SpP-2
GtP- 1
PA 3
LS-0
PA-5
PA-6
LS- 1
BN 50
TM 15
TM 16
1988
1995
1986
1979
1990
M&A
McDon
M&A
Olker
Kilian
Kilian
Kilian
Kilian
Olker
Kilian
Olker
Olker
45.96 0.18 4.06 7.54 0.20 37.78 3.21 0.33 0.26 99.92 89.9
46.12 0.18 4.09 7.49 0.15 37.77 3.23 0.36 0.03 0.38 0.25 100.5 89.9
46.20 0.23 4.75 7.70 0.13 35.50 4.36 0.40 0.43 0.23 99.93 89.2
45.10 0.20 3.30 8.00 0.15 38.10 3.10 0.40 0.40 98.75 89.5
44.8 0.21 4.45 8.40 0.14 37.2 3.60 0.34 0.03 0.43 0.24 99.84 88.8
44.15 0.07 1.96 8.28 0.12 42.25 2.08 0.11 0.05 0.44 0.27 99.78 90.1
44.0 0.09 2.27 8.43 0.14 41.40 2.15 0.24 0.05 0.39 0.27 99.43 89.8
44.99 0.06 1.40 7.89 0.11 42.60 0.82 0.05 0.11 0.32 0.26 99.79 90.6
43.95 0.05 1.03 7.58 0.12 44.86 0.79 0.02 0.02 0.46 0.32 99.15 91.3
44.79 0.04 1.00 7.23 0.12 45.13 0.68 0.07 0.00 0.46 0.27 99.78 91.8
43.96 0.04 0.95 7.14 0.11 45.30 0.88 0.06 0.00 0.42 0.29 99.13 91.9
44.49 0.02 0.87 7.21 0.11 45.96 0.63 0.01 0.01 0.31 0.28 99.91 91.9
43.31 0.04 0.52 6.80 0.10 47.64 0.40 0.00 0.00 0.34 0.33 99.48 92.6
42.23 0.16 3.83 9.56 0.13 41.00 0.87 0.00 0.00 0.79 0.32 98.88 88.4
42.25 0.17 3.99 9.33 0.13 40.74 0.98 0.01 0.00 0.81 0.32 98.74 88.6
44.92 0.13 2.97 9.24 0.13 40.01 0.69 0.04 0.00 0.33 0.27 98.73 88.5
47.34 0.23 3.27 8.73 0.13 39.06 0.81 0.05 0.09 0.37 0.24 100.32 88.9
4~ Oe
Lherz
t-,a
Garnet lherzolites
Garnet-spinel lherzolites
LS101
SiO 2 TiO 2 A120 3 FeOto t MnO MgO CaO Na20 K 20 Cr20 3 NiO Sum Mg#
Spinel harzburgites
LS33
Olker
Stern
Kilian
Olker
Stern
Kilian
44.04 0.08 2.77 7.96 0.13 41.27 1.81 0.11 0.00 0.38 0.32 98.87 90.2
45.60 0.12 3.90 8.20 0.16 37.90 3.00 0.25 0.00 0.42 0.32 99.97 89.2
44.20 0.09 1.50 8.02 0.11 42.12 2.57 0.21 0.00 0.28 0.27 99.37 90.4
44.81 0.11 3.37 7.60 0.13 39.39 2.28 0.15 0.00 0.46 0.26 98.56 90.2
44.80 0.16 3.90 8.10 0.14 37.30 3.00 0.26 0.00 0.42 0.25 98.33 89.1
45.65 0.13 3.48 7.59 0.13 39.23 2.65 0.19 0.00 0.43 0.24 99.71 90.2
BN4
BN35
BNH12
LS4
Pal
TM0
TM1
Stern
Stern
Olker
Stern
Olker
Olker
Stern
Olker
Stern
Olker
aver.
45.40 0.25 4.30 8.30 0.14 37.10 3.30 0.30 0.00 0.30 0.24 99.57 88.9
43.86 0.14 2.10 8.83 0.12 40.81 2.30 0.16 0.02 0.45 0.29 99.07 89.2
44.90 0.20 3.80 7.90 0.12 38.20 2.90 0.22 0.00 0.49 0.28 99.01 89.6
44.01 0.16 3.59 7.85 0.11 39.45 3.06 0.27 0.00 0.41 0.26 99.17 90.0
44.63 0.15 2.86 8.01 0.12 39.21 3.12 0.28 0.00 0.34 0.27 98.99 89.7
45.00 0.20 4.10 8.20 0.15 37.60 3.20 0.31 0.00 0.33 0.28 99.37 89.1
44.20 0.15 3.66 7.89 0.13 38.33 3.05 0.25 0.01 0.38 0.25 98.30 89.7
45.30 0.17 4.00 8.60 0.14 37.20 3.00 0.27 0.00 0.39 0.32 99.39 88.5
44.00 0.12 2.75 8.22 0.12 39.98 2.61 0.20 0.00 0.31 0.26 98.57 89.7
44.74 0.15 3.39 8.11 0.13 38.91 2.84 0.23 0.00 0.39 0.27 99.17 89.5
45.30 0.20 4.60 8.70 0.18 36.90 3.40 0.29 0.00 0.41 0.26 100.24 88.3
TM2
PA
t,,a tal
224
C.R. Stern et al. / Lithos 48 (1999) 217-235
4), only the AI content of orthopyroxene grains is zoned. These different core-to-tim chemical zonation
not contain a broad homogeneous core (LS 101; Fig. 4). In the highest temperature xenoliths (LS33; Fig.
gt-peridotite I
I
sp-harzburgites I
I
I
I
I
LS~ I
I
225
C.R. Stern et al. / Lithos 48 (1999) 217-235
patterns are significant for the interpretation of the complexities of the thermal history of the mantle lithosphere below the Pali-Aike volcanic field. Table 1 presents previously published (Stem et al., 1989) and new major element chemical analysis of 18 vein-free peridotite xenoliths from Pali-Aike including both garnet-bearing and garnet-free lherzolites and harzburgites, as well as the average composition of Pali-Aike garnet-bearing lherzolites, other published averages of continental spinel and garnet peridotites, and estimates of the major element composition of primitive mantle. Pali-Aike garnet-bearing lherzolites have major-element compositions similar to estimates of primitive mantle, and significantly higher CaO and A120 3, and lower M g # compared to previously published compilations of the average composition of either spinel or garnet lherzolites from continental lithosphere (Fig. 5). Compared to Pali-Aike garnet lherzolites, spinel harzburgites have lower CaO and A120 3, and higher M g # (Fig. 5), consistent with significant amounts of melt extraction (McDonough, 1990). Garnet-bearing harzburgites, in contrast, have lower CaO, but not lower A12 O 3 or higher Mg # . Modal metasomatism has produced veins containing high-Ti phlogopite _+ pargasitic amphibole _+ ilmenite in some peridotite xenoliths (sample TM15 in Fig. 3), as well as disseminated phlogopite and amphibole (Stern et al., 1986, 1989). Such veins are more abundant in moderate- and high-temperature ( > 970~ xenoliths than in low-temperature ones. The volume of vein material may be up to 3% in some xenoliths. This metasomatism has added Ti, K, and Na, as well as H 2 0 and some trace-elements to the mantle, which is not reflected in the major element analysis of the vein-free peridotites presented in Table 1.
Table 2 Trace-element contents, in ppm, of garnet and clinopyroxene in fertile high-temperature garnet lherzolites LS101 and LS33, and infertile moderate-temperature spinel harzburgite Pa5. Determined by LAM-ICP-MS at Memorial University, Newfoundland. Class standards NBS612 and BCR2 were used for calibration. Techniques described by Jackson et al. (1992) and Taylor et al. (1996) Sample LS101 LS33 LS101 LS33
PA5
PA5
Mineral gt-core gt-core cpx-core cpx-core cpx-core cpx-rim Th U Nb Ta La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
0.14 0.05 1.35 0.04 0.03 0.65 0.21 2.16 2.63 1.15 6.29 2.06 19.68 6.17 20.71 3.88 24.54 3.99
0.01 0.02 1.21 0.04 0.05 0.59 0.20 2.11 2.85 1.57 6.73 1.80 14.18 3.97 11.80 2.22 12.73 2.06
0.05 0.01 0.85 0.18 1.69 6.98 1.06 4.28 1.42 0.50 1.37 0.20 0.82 0.14 0.20 0.03 0.35 0.02
0.06 0.01 0.61 0.09 1.57 5.55 0.99 5.31 1.40 0.49 1.84 0.28 1.42 0.28 0.66 0.10 0.47 0.05
0.03 < 0.01 0.48 0.08 0.97 4.27 0.89 4.39 1.69 0.59 1.84 0.29 1.38 0.22 0.47 0.06 0.24 0.04
0.32 0.08 3.77 0.40 4.36 11.36 1.97 8.82 2.66 0.89 2.52 0.39 1.74 0.31 0.63 0.08 0.47 0.05
2.2. T r a c e - e l e m e n t a n d isotope chemistry
Stem et al. (1989) determined that fertile garnetbearing lherzolites from Pali-Aike have whole-rock S m / N d , 87Sr/S6Sr and 143Nd/144Nd ratios similar to mid-ocean ridge basalts. New laser ablation microprobe-inductively coupled p l a s m a - m a s s spectrometry ( L A M - I C P - M S ) analysis of trace-elements in clinopyroxene and garnet (Table 2; Fig. 6), and of the Sr and Nd isotopic composition of leached
Fig. 5. Whole-rock CaO and A1203 contents of Pali-Aike xenoliths (open symbols) plotted against Mg# and compared with both different estimates for the Primitive Mantle (solid diamonds, data from Table 1; PM1, Hofmann, 1988" PM2, All~gre et al., 1995; PM3, Palme and Nickel, 1985; PM4, Ringwood, 1979; PM5, McDonough, 1990), and published compilations of the average compositions of continental spinel and garnet peridotite xenoliths (solid squares, data from Table 1; SpP-1 and GtP-1, MaalCe and Aoki, 1975; SpP-2, McDonough, 1990). Samples with multiple analysis (LS33, LS101, TM1, TM2 and BN50) are connected by dashed lines and the average of Pali-Aike garnet lherzolites is indicated by the solid square PA. The figure illustrates the major element similarity between fertile garnet-bearing lherzolites from Pali-Aike and estimates of Primitive Mantle, and significant differences between these lherzolites and both garnet and spinel harzburgites.
226
C.R. Stern et al./Lithos 48 (1999) 217-235 Infertile spinel harzburgites h a v e similar O isotopic c o m p o s i t i o n s as garnet-bearing lherzolites (Table 6; Fig. 7), but they h a v e significantly l o w e r w h o l e - r o c k Sr, N d and S m concentrations, S m / N d and 143Nd/144Nd ratios, and higher 87Sr/S6Sr ratios
i
(Table 3; Fig. 7). The N d and Sr isotopic ratios of these xenoliths are similar to Q u a t e r n a r y alkali olivine basalts from P a t a g o n i a (Fig. 7) and within the m a n t l e array defined by oceanic basalts ( S t e m et al., 1989). The Os isotopic c o m p o s i t i o n of one infertile spinel harzburgite indicates an older m o d e l age for this s a m p l e c o m p a r e d to the fertile garnet lherzolites. High-Ti p h l o g o p i t e and pargasitic a m p h i b o l e f r o m m e t a s o m a t i c veins within Pali-Aike xenoliths h a v e
Table 3 Rb, Sr, Nd and Sm concentrations, in ppm, and Sr and Nd isotopic compositions of Pali-Aike peridotites (WR = whole-rock; Gt = garnet; Sp = spinel; Cpx = clinopyroxene; Phlg = phlogopite mica; Amp = amphibole) Sample Fig. 6. Trace-element compositions, normalized to chondritic abundances (Taylor and McLennan, 1985), of both cores (solid symbols) and rims (open symbols) of garnet and clinopyroxene in spinel and garnet peridotites (Table 2). Minerals in fertile, high temperature, garnet lherzolites are unzoned, while those in the infertile, lower temperature spinel harzburgites show rim enrichment of the more incompatible elements.
c l i n o p y r o x e n e and garnet separates from garnetbe a r in g lherzolites (Table 3; Fig. 7), c o n f i r m this conclusion. For garnet and c l i n o p y r o x e n e in garnet lherzolite LS33, N d and S m concentrations m e a s u r e d i n d e p e n d e n t l y by L A M - I C P - M S and isotope dilution M S differ by < 10%. N e w Pb (Table 4; Fig. 8), Os (Table 5), and O ( T a b l e 6; Fig. 7) isotopic analysis also indicate that P a li- A i k e garnet lherzolites are isotopically similar to M O R B . W h o l e - r o c k O isotopic c o m p o s i t i o n s w e r e calculated f r o m m e a s u r e d mineral values and estim a t e d m o d a l proportions. Inter-mineral differences in 6180 h a v e b e e n d i s c u s s e d by K y s e r (1990). Rhen i u m depletion ages for garnet lherzolites, calculated a s s u m i n g R e / O s = 0, range from 0 to 860 M a (Table 5), s u g g e s t i n g a late Proterozoic to P h a n e r o z o i c age for the m a n t l e lithosphere b e l o w s o u t h e r n m o s t South A m e r i c a , consistent with the P h a n e r o z o i c age of the crustal rocks is this region ( R a m o s , 1988).
Rb
Sr
87Sr/ 86Sr
Nd
Sm
143Nd/ 144Nd
Garnet peridotites (unueined) LS-33WR 0.23 14.4 0.70298 0.942 0.295 0.51296 LS-33 Cpx 0.07 87.3 0.70298 5.34 1 . 3 7 0.51298 LS-33 Gt 0.02 0.31 2.04 2.49 0.51295 Spinel + garnet peridotites (unueined) TM-0 Cpx 82.2 0.70264 TM-1 WR1 0.16 13.6 0.70292 TM-1 WR2 0.26 12.0 0.70289 TM-2WR 0.16 12.7 0.70270
4.94 0.840 0.718 0.802
0.324 0.278 0.252
0.51313 0.51303 0.51303 0.51297
Spinel peridotites (unueined) LS-2WR 0.28 6.95 LS-20WR 0.08 4.85 LS-6WR 2.80 X-3 WR 6.32 BN-71 WR 2.54 BN-71 Cpx 0.02 61.8
0.391 0.436 0.200 0.371 0.202 3.83
0.097 0.099 0.042 0.051 1.28
0.51278 0.51281 0.51284 0.51281 0.51291 0.51288
Modally metasomatized (veined) peridotites BN-35 WRa 0.24 13.5 0.70338 1.136 BN-72 WRa 6.81 0.70350 0.493 BN-44 WRa 0.70343 TM-16 Cpx a 94.9 0.70324 TM- 16 Phlg 0.70336 TM-15 Cpx a 0.22 68.0 0.70325 4.58 TM- 15 Amp 20.2 251.3 0.70329 5.28 TM-15 Phlg 201 52.4 0.70344 BN-63 Phlg 248 33.2 0.70344 0.309 BN-40 Phlg 230 32.7 0.70343 -
0.374 0.112 1.56 2.03 0.071 -
0.51284 0.51285 0.51287 0.51301 0.51292 0.51308 0.51293 0.51291 0.51284 0.51287
a WR
0.70362 0.70365 0.70373 0.70431 0.70349 0.70345
and Cpx measured for material outside the vein.
227
C.R. Stern et al./Lithos 48 (1999) 217-235
1
l
I
!
I
I
1
1 ~ ] .
Fig. 7.87Sr/86Sr vs. 143Nd/144Nd and 8180 (per mil) of both whole-rock (shaded symbols) and minerals (open symbols) from Pali-Aike peridotite xenoliths compared to MORB (Bach et al., 1994), Patagonian plateau alkali basalts (Stem et al., 1990) and Andean arc basalts (Futa and Stem, 1988; Lopez-Escobar et al., 1993). Unveined garnet lherzolites have Sr, Nd and O isotopic compositions similar to MORB. Vein phlogopite and amphibole, and modally metasomatized lherzolites, have isotopic compositions more similar to Pali-Aike and other Patagonian plateau alkali basalts, as do cryptically metasomatized spinel harzburgites.
C.R. Stern et al. / Lithos 48 (1999) 217-235
228
Table 4 U, Th and Pb concentrations, in ppb, and Pb isotopic compositions of minerals in Pali-Aike peridotite xenoliths (Gt = garnet; Sp = spinel; Cpx = clinopyroxene; Phlg = phlogopite mica) Sample
U
Th
Pb
206P b / 204Pb
207P b / 204Pb
Table 5 Os concentrations, isotopic ratios and "rhenium depletion" model ages for Pali-Aike xenoliths Sample
208P b / 204Pb
12.67 8.77
57.56 10.21
27.24 18.07 0.93 18.26
15.40 15.39
1870S/ 1880sa
Model ages (Ma) b
Garnet peridotite
Garnet peridotites (unveined) LS-33 Cpx LS-33 Gt
Os (ppb) a
LS-33 TM-17
37.61 37.77
2.748 2.992
0.1231 0.1282
860 140
0.1280 0.1293 0.1255
173 0 531
0.1185
1500
Spinel 4- garnet peridotite Spinel + garnet peridotites (unveined) TM-0 Cpx
46.13
190.50
83.70 18.40
15.49
38.00
15.56 15.57 15.62
38.51 38.50 38.80
TM-0 TM-1 TM-2
0.774 1.543 2.568
Modally metasomatized (veined) peridotites TM-16Cpx 13.47 46.22 61.62 18.95 TM-16 Phlg 103.7 423 18.77 BN-96 Phlg 360 19.23
Spinel peridotite BN-71
3.227
aDetermined as described in Hauri and Hart (1993). bRe-Os model ages calculated assuming R e / O s = 0 as described by Walker et al. (1989).
Nd, Pb and O isotopic compositions similar to PaliAike and other Patagonian alkali olivine basalts (Tables 3, 4 and 6; Figs. 7 and 8). 87Sr/86Sr ratios in
phlogopites are higher than both co-existing amphibole and Pali-Aike basalts, but this may reflect their
Patagonian plateau basalts
Q..
t,-. o o4
m
~ 9
LS33-grt I
I
I
I
I
Fig. 8. 2~176 vs. 2~176 for minerals from Pali-Aike mantle xenoliths compared to Pacific MORB (Bach et al., 1994; Klein and Karsten, 1995), Patagonian plateau alkali basalts (Stern et al., 1990), and Andean arc basalts (Lopez-Escobar et al., 1993). Fertile garnet-bearing lherzolites (LS33 and TM0) have Pb isotopic compositions similar to MORB, while metasomatic vein phlogopite and clinopyroxene in a xenolith (TM16) with veins have Pb isotopic compositions within the field of Pali-Aike and other Patagonian plateau alkali basalts.
C.R. Stern et al./Lithos 48 (1999) 217-235
229
Table 6 6 1 8 0 a n d 6 D , i n p a r t s - p e r - m i l , f o r m i n e r a l s i n P a l i - A i k e x e n o l i t h s (O1 = o l i v i n e ; O p x = o r t h o p y r o x e n e ; C p x = c l i n o p y r o x e n e ; G t = g a r n e t ; S p --- s p i n e l ; P h l g = p h l o g o p i t e m i c a ; A m p h = p a r g a s i t i c a m p h i b o l e ; W R = w h o l e - r o c k c a l c u l a t e d b a s e d o n m o d a l p r o p o r t i o n s o f c o n s t i t u e n t minerals) Sample
O1
Opx
Cpx
Gt
Sp
Amph
Phlog
6D
WR*6180
5.5
6.2
.
.
.
.
6.0
6.0
5.9
.
.
.
.
5.9
Garnet peridotites (unveined) LS-33
6.4
5.5
Spinel + garnet peridotites (unveined) TM-1
5.8
6.0
Spinel peridotites (unveined) LS-2
6.1
6.1
5.7
.
LS-6
6.0
6.0
5.9
-
.
. 5.1
.
.
.
.
6.0
.
-
6.0
LS-20
5.8
5.7
5.5
.
BN-71
6.3
5.4
5.4
-
5.4
-
-
. -
6.0
5.8
X-3
5.8
5.6
5.8
-
5.0
-
-
-
5.8
Modal metasomatized (veined) peridotites BN-35
6.1
6.2
5.2
6.0
5.4
- 112
6.0
BN-55
5.6
5.5
-
5.9
5.4
-56
5.6
BN-72
6.1
5.3
5.6
-
5.5
BN-44
5.2
5.4
-
-
BN-40
5.0
5.4
-
-
BN-51
5.4
5.5
-
-
BN-46
-
5.4
-
6.0
BN-42
-
5.2
-
5.4
6.4
-
5.3
BN-13
-
6.3
-
5.7
5.8
-
6.0
Above
5.9
5.5
-
5.8
-
5.7
Vein
-
6.1
-
-
6.8
-
6.5
Vein
.
6.5
-
6.5
Below
5.5
-
5.7
-
5.6
-
5.4
-
5.9
5.5
-66
5.3
5.7
- 125
5.2
5.7
-56
5.5
5.5
-67
5.6
TM-14
.
. 5.5
-
. -
TM-15 Vein
5.7
5.3
-
5.4
Below
5.2
5.3
-
-
-
-
-
5.2
Away
5.6
5.3
-
-
-
-
-
5 . 5
5.2
5.4
Eclogite / pyroxenite BN-49
-
-
5.5
5.9
-
-
-
5 . 7
BN-25
-
5.9
-
5.8
-
-
-
5 . 9
LS-3
-
5.3
-
5.0
-
-
-
BN-35
6.1
6.2
5.2
6.0
-
high R b / S r ratios (Stern et al., 1989). These modal metasomatic minerals are isotopically unlike Andean arc basalts, as are Pali-Aike alkali basalts (Stern et al., 1990), and provide no evidence for the introduction of any slab-derived fluids into the continental lithosphere below the Pali-Aike volcanic field, which is located > 200 km east of the Andean arc of andesitic volcanoes (Fig. 1). Also, no highly radiogenic phases preserving heterogeneities produced by
5.4
- 112
5.2 6.0
ancient enrichment events occur in the Pali-Aike xenoliths. Clinopyroxenes separated from close to veins in two modally metasomatized garnet-bearing peridotites (TM15 and TM16; Tables 3 and 4) have Sr and Pb isotopic compositions similar to vein minerals, but Nd isotopic compositions more similar to unveined garnet-bearing peridotites (Figs. 7 and 8), possibly reflecting the relatively high Sr and Pb
230
C.R. Stern et al./Lithos 48 (1999) 217-235
content of vein minerals relative to peridotite. Oxygen isotopes of minerals in and around a vein in one sample (TM15; Table 6) appear to have equilibrated, while in another vein (TM14) they have not (Kyser, 1990). These data suggest variable amounts of centimeter-scale diffusion of these elements from the veins into the surrounding mantle, with diffusion rates for different elements presumably dependent on concentration gradients and temperature. L A M - I C P - M S analysis indicate that the traceelement composition of cores of clinopyroxenes in spinel harzburgites are similar to those of clinopyroxenes in garnet lherzolites. However, incompatible trace-elements are enriched at the rims compared to the cores of the clinopyroxenes in these low- and moderate-temperature spinel harzburgites (Fig. 6). This suggests possibly meter to kilometer-scale cryptic metasomatism, since these xenolith typically contain no evidence of modal metasomatism. Although the concentration of modal metasomatic veins is greatest among high-temperature xenoliths derived from the deepest portion of the lithosphere, such zoning in high-temperature garnet lherzolites is apparently absent within detection limits (Fig. 6). This may reflect the more rapid diffusion and equilibration rates at higher temperatures deeper in the mantle.
3. Discussion and conclusions The core-to-rim chemical zonation of orthopyroxenes (Fig. 4) suggest a complex thermal history for
the Pali-Aike peridotite xenoliths, as does the textural evidence for the reaction spinel + pyroxene garnet + olivine preserved in spinel + garnet peridotites, and the reverse reaction as indicated by spinel and pyroxenes in kelyphitic rims around some garnets (Fig. 3). Since diffusion and exchange of Mg between pyroxenes is more rapid than Ca diffusion, and the Ca diffusion is slower in orthopyroxene than clinopyroxene (Sautter and Harte, 1988; WittEickschen and Seck, 1991; Werling and Altherr, 1997), we have used the differences in the T estimates based on the Ca-in-orthopyroxene thermometer compared to the two-pyroxene thermometer (Brey and KiShler, 1990) to constrain the thermal history of the Pali-Aike xenoliths (Fig. 9). Fig. 4 shows that for the spinel harzburgite LS2, the temperatures estimated by the Ca-in-orthopyroxene thermometer decrease from the core to the rim by 135~ In contrast, temperatures estimated by the two-pyroxene thermometer are uniform throughout the crystal, and 175~ (_+ 32~ lower in the core compared to those estimated by the Ca-in-orthopyroxene thermometer. We interpret these differences as due to incomplete equilibration of Ca in orthopyroxene compared to Mg exchange between the two pyroxenes during cooling of the xenolith LS2 by at least 175~ (Fig. 9a). Other indications of significant cooling of the lithosphere below Pali-Aike include both the textural evidence for the reaction spinel + pyroxene ~ garnet + olivine preserved in the spinel + garnet peridotites (Fig. 3), and the exsolution of clinopyroxene from orthopyroxene, and vice versa, observed in many low-temperature ( < 970~ based
Fig. 9. P - T history of the lithosphere below southern South America, based on mineral thermometry (Fig. 4), mineralogic evidence for reactions due to either heating or cooling, and geologic constraints which indicate 7 km of sedimentation in the Magellanes basin since the Jurassic breakup of Gondwanaland (Biddle et al., 1986), when widespread magmatic mafic and silicic magmatic activity associated with extension heated and thinned the lithosphere (Bruhn et al., 1978). Subsequent to this heating event, an early period of long term cooling, of up to 175~ (arrow a; Fig. 9a), is documented in low-T spinel peridotites (LS2, Fig. 4) and websterites (open square) by differences between core temperatures, estimated with the Ca-in-orthopyroxene thermometer, compared to rim temperatures, estimated with the two-pyroxene thermometer (Fig. 4 and inset). This cooling also produced the reaction spinel + pyroxene ~ garnet + olivine, as spinel lherzolites cooled across the dotted reaction line separating spinel from garnet peridotites (Webb and Wood, 1986). Prior to cooling, the subcontinental geotherm was similar to the 75 mW m - 1 geotherm of Chapman (1986), and the lithosphere was approximately 80 km thick. After cooling the geotherm was closer to the 65 mW m -1 geotherm (Fig. 2). Recent heating of up to > 65~ (arrow b; Fig. 9b) is documented in high-temperature garnet-bearing peridotites (open triangles and circles) by differences between core temperatures, estimated with the Ca-in-orthopyroxene thermometer, compared to rim temperatures, estimated with the two-pyroxene thermometer (Fig. 4 and inset). This heating, which may be related to the generation of the Pali-Aike basalts, also produced spinel + pyroxene in kelyphitic rims surrounding garnets, and has thinned the lithosphere to < 100 km.
231
C.R. Stern et al./Lithos 48 (1999) 217-235
on the two-pyroxene thermometer) pyroxenites, websterites and spinel peridotites. Selverstone and Stern
(1983) also documented cooling in deep-crustal metabasic granulite xenoliths, based on both mineral
" ~~~
/
~~~
-
current
ridotites
~
232
C.R. Stern et al. / Lithos 48 (1999) 217-235
thermometry and fluid inclusions in granoblastic pyroxenes compared to pyroxenes in symplectic intergrowths formed by reaction of plagioclase and olivine. The timing of this cooling event is uncertain, but for similar chemical zonation patterns in orthopyroxenes within low-T (--800~ peridotite xenoliths from the East African Rift system, Garasic (1997) calculated cooling times of 200 to 500 Ma based on cation diffusion models for Ca and A1 in orthopyroxene. This suggests that the chemical zonations observed in orthopyroxenes within low-T Pali-Aike xenoliths reflect slow, long-term cooling. Geologic constraints suggest that long-term cooling has occurred below southernmost South America since the Jurassic, when widespread mafic and silicic volcanism was associated with the extensional break-up of Gondwanaland (Bruhn et al., 1978). Since this event the area in which the Pali-Aike basalts erupted has been a slowly subsiding sedimentary basin without any magmatic activity until the Quaternary (Biddle et al., 1986). In contrast to the low-T xenoliths, chemical zoning in orthopyroxene within high-T garnet peridotites (Fig. 4) suggests a heating event. In garnet lherzolites, temperatures estimated by the Ca-in-orthopyroxene thermometer increase from core-to-rims, and temperatures estimated by the two-pyroxene thermometer are uniformly higher. The difference between core temperatures estimated by the Ca-inorthopyroxene thermometer, compared to rim temperatures estimated by the two-pyroxene thermometer, is 65~ (_+ 32~ for garnet lherzolite LS33, the highest temperature xenolith documented from PaliAike (Figs. 2 and 4). Some garnet-bearing lherzolites show core-to-rim temperature increases up to 90~ (Fig. 9b). However, the flat and/or parabolic shape of the Ca zonation pattern in orthopyroxenes within high-T gamet lherzolites (Fig. 4), suggests that the lowest temperatures reached by these xenoliths prior to heating is not preserved in the core composition, and the amount of heating calculated is a minimum. Other evidence for heating of high-T garnet-bearing peridotites are kelyphitic rims, containing spinel and pyroxenes, developed around garnets. This indicates the occurrence of the reaction garnet + olivine spinel + pyroxene, which implies either heating (Fig. 9b) or decompression. These kelyphitic rims occa-
sionally contain unzoned grains of pargasitic amphibole similar in composition to amphibole both in veins and occurring as isolated grains, which suggests that these rims did not form solely during decompression associated with the transport of the xenoliths to the surface. Based on the significantly higher diffusion rates of Ca and A1 at high temperatures, this heating event is considered to be a more recent event, possibly related to the generation of the Pali-Aike basalts, than the cooling which produced the inverse chemical zonation patterns in orthopyroxenes within low-T Pali-Aike xenoliths. The low-T xenoliths apparently have not yet been affected by this heating. The different zonation patterns of Ca and A1 in orthopyroxenes of both low- and high-temperature xenoliths which occur together in the same host basalts, as well as the shape of the zonation patterns in the high-T xenoliths, argue against the possibility that the recent heating of the high-T peridotites was caused during xenolith transport to the surface in the host magma. We conclude that after the Jurassic, when it was thinned by extensive magmatic activity and extension, the lithosphere below southemmost South America cooled by as much as 175~ and thickened from approximately 80 to 100 km (Fig. 9a). More recently, it has been heated by a minimum of 65~ and thinned again to < 100 km (Fig. 9b). Since element diffusion and equilibration is strongly temperature dependent (Crank, 1975; Jurewicz and Watson, 1988), evidence for the earlier cooling event is preferentially preserved in low-temperature xenoliths from shallower in the mantle, while evidence for the more recent heating event is reflected in high-temperature xenoliths from deeper in the mantle. From a global perspective, these changes in geothermal gradient and thickness are relatively minor, and no evidence preserved in the Pali-Aike xenoliths suggests that the subcontinental lithosphere beneath southernmost South America was ever significantly thicker than oceanic lithosphere beneath > 100 Ma oceanic crust. Its current geothermal gradient and lithospheric thickness is more similar to oceanic lithosphere than Archean continental lithosphere. Furthermore, the types of lithologies found among the Pali-Aike peridotite xenoliths, and their vertical distribution in the lithosphere as deduced from the
233
C.R. Stern et al./Lithos 48 (1999) 217-235
-
"
'e"
~
Po'
'
'bee e e
,.
",
9
r
"-k
Fig. 10. Lithologic zonations, modified after Stem et al. (1986, 1989), of the continental lithosphere of southernmost South America as suggested by the calculated temperature and pressure of equilibration of Pali-Aike xenoliths. Mafic granulites occur in the deeper portion of the continental crust (Selverstone and Stem, 1983). Infertile spinel harzburgites are predominant in the upper and middle section of mantle, whereas the deepest portion of the lithosphere consists dominantly of fertile garnet lherzolites. The lower lithosphere was modified by both modal and cryptic metasomatism related to the generation of the Pali-Aike basalts.
234
C.R. Stern et al./Lithos 48 (1999) 217-235
estimates of their temperature and pressure (Fig. 10), are similar to that expected for oceanic lithosphere, and different from that described for Archean continental lithosphere (Stern et al., 1986, 1989; HenjesKunst and Altherr, 1992). Low-temperature ( < 970~ xenoliths from the shallow portion of the mantle lithosphere are predominantly infertile spinel harzburgites. Although some harzburgites also occur among moderate- and high-temperature ( > 970~ xenoliths, these high-temperature xenoliths from the deeper portion of the lithosphere are predominantly fertile spinel + garnet and garnet lherzolites with trace-element and isotopic compositions similar to the mantle source of mid-oceanic ridge basalts. This implies a significant continuous chemical and density gradient, over a relatively short vertical distance of a few tens of kilometers, with decreasing olivine and increasing clinopyroxene and garnet content, and thus increasing density with depth. The apparent continuous nature of the vertical transition in the upper 50 km of the mantle below southernmost South America, from infertile harzburgite to more fertile lherzolite (Fig. 10), has been explained by magma extraction from the shallow portion of the lithosphere at a late Proterozoic midoceanic spreading center, prior to the tectonic capture and accretion of this mantle section to the western margin of Gondwanaland during the Paleozoic (Stern et al., 1986, 1989). R e / O s model ages (Table 5) are consistent with this explanation. An alternative model, in which the lower fertile portion of this lithosphere has been underplated below older, refractory lithosphere, may be possible, but nevertheless, no evidence exists that the shallow refractory portion of this lithosphere was ever greater in thickness than 80 km. In summary, there is no evidence from the PaliAike xenoliths for the existence of a thick, olivinerich, lithospheric mantle root below southernmost South America, either currently or in the past. The highest temperature garnet lherzolites derived from the deepest sampled portion of this lithosphere are mineralogically and chemically similar to the global asthenospheric source of MORB, and the transition from lithosphere to asthenosphere, which currently occurs at < 100 km, must reflect temperature and rheology rather than chemistry and/or density. The mineralogic evidence for a multi-stage thermal his-
tory of this lithospheric section suggests that this temperature/rheology dependent transition between the lithosphere and asthenosphere below southernmost South America has migrated both upwards and downwards by a few tens of kilometers with time, and that the current lithosphere cannot be considered a permanent root.
Acknowledgements The xenoliths from the Pali-Aike volcanic field were first discovered and collected in collaboration with Alexandra Skewes. Early stages of analytical work on these xenoliths was supported by NSF grants EAR79-11204 and EAR83-13884, and recent work by German Research Foundation grant AL166/10.
References All~gre, C.J., Poirier, J.P., Humler, E., Hofmann, A.W., 1995. The chemical composition of the earth. Earth Planet. Sci. Lett. 134, 515-526. Bach, W., Hegner, E., Erzinger, J., Satir, M., 1994. Chemical and isotopic variations along the superfast spreading East Pacific Rise from 6 to 30~ Contrib. Mineral. Petrol. 116, 365-380. Biddle, K.T., Uliana, M.A., Mitchum, R.M. Jr., Fitzgerald, M.G., Wrigth, R.C., 1986. The stratigraphic and structural evolution of the central and eastern Magallanes Basin, southern South America. Int. Assoc. Sedimentol., Spec. Publ. 8, 41-61. Brey, G.P., KiShler, T., 1990. Geothermobarometry in four-phase lherzolites: II. New thermobarometers, and practical assessment of existing thermobarometers. J. Petrol. 31, 1353-1378. Bruhn, R.L., Stem, C.R., de Wit, M.J., 1978. Field and geochemical data bearing on the development of a Mesozoic volcanotectonic rift zone and back-arc basin in southernmost South America. Earth Planet. Sci. Lett. 41, 32-46. Cande, S.C., Leslie, R.B., 1986. Late Cenozoic tectonics of the southern Chile Trench. J. Geophys. Res. 91,495-520. Chapman, D.S., 1986. Thermal gradients in the continental crust. In: Dawson, J.B., Carswell, D.A., Hall, J., Wedepohl, K.H. (Eds.), The Nature of the Lower Continental Crust. Geol. Soc. London, Spec. Publ. 24, pp. 63-70. Crank, J., 1975. The Mathematics of Diffusion. Oxford Univ. Press, London. de Wit, M.J., 1977. The evolution of the Scotia arc as a key to the reconstruction of Gondwanaland. Tectonophysics 37, 53-81. Douglas, B.J., Saul, S.L., Stem, C.R., 1987. Rheology of the upper mantle beneath southernmost South America inferred from peridotite xenoliths. J. Petrol. 95, 241-253. Futa, K., Stem, C.R., 1988. Sr and Nd isotopic and trace element
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compositions of Quaternary volcanic centers of the southern Andes. Earth Planet. Sci. Lett. 88, 253-262. Garasic, V., 1997. Mantelxenolithe als Dokumente der thermischen Entwicklung des Erdmantels unter den Chyulu Hills, Kenia. PhD Thesis. Univ. Heidelberg, 220 pp. Hauri, E.H., Hart, S.R., 1993. Re-Os isotope systematics of HIMU and EMII oceanic island basalts from the south Pacific Ocean. Earth Planet. Sci. Lett. 114, 353-371. Henjes-Kunst, F., Altherr, R., 1992. Metamorphic petrology of xenoliths from Kenya and northern Tanzania and implications for geotherms and lithospheric structures. J. Petrol. 33, 11251156. Hofmann, A.W., 1988. Chemical differentiation of the Earth: relationship between mantle, continental crust and oceanic crust. Earth Planet. Sci. Lett. 91,271-285. Jackson, S.E., Longerich, H.P., Dunning, G.R., Fryer, B.J., 1992. The application of laser ablation microprobe-inductively coupled plasma-mass spectrometry ( L A M - I C P - M S ) to in situ trace element determinations in minerals. Can. Mineral. 30, 1049-1064. Jurewicz, A.J.G., Watson, E.B., 1988. Cations in olivine: Part 2. Diffusion in olivine xenocrysts, with applications to petrology and mineral physics. Contrib. Mineral. Petrol. 99, 186-201. Klein, E.M., Karsten, J.L., 1995. Ocean-ridge basalts with convergent-margin geochemical affinities from the Chile Ridge. Nature 374, 52-57. Kyser, T.K., 1990. Stable isotopes in the continental lithospheric mantle. In: Menzies, M. (Ed.), Continental Mantle. Oxford Univ. Press, pp. 127-156. Lopez-Escobar, L., Kilian, R., Kempton, P.D., Tagiri, M., 1993. Petrology and geochemistry of Quaternary rocks from the Southern Volcanic Zone of the Andes between 41o30 ' and 46~ Chile. Rev. Geol. Chile 20, 33-56. Maalce, S., Aoki, K.I., 1975. The major element composition of the mantle estimated from the composition of lherzolites. Contrib. Mineral. Petrol. 63, 161-173. McDonough, W.F., 1990. Constraints on the composition of the continental lithospheric mantle. Earth Planet. Sci. Lett. 101, 1-18. McKenzie, D., Bickle, M.J., 1988. The volume and composition of melt generated by extension of the lithosphere. J. Petrol. 29, 625 -679. Nickel, K.G., Green, D.H., 1985. Empirical geothermobarometry for garnet peridotites and implications for the nature of the lithosphere, kimberlites and diamonds. Earth Planet. Sci. Lett. 73, 158-170. Olker, B., 1997. Druck-Temperatur-Absch~itzungen an Mantelxenolithen von Pali-Aike, siidliches Siidamerika. Unpublished Diploma Thesis. Univ. Heidelberg, 97 pp. Palme, H., Nickel, K.G., 1985. Ca/A1 ratio and composition of the Earth's upper mantle. Geochim. Cosmochim. Acta 49, 2123-2132. Ramos, V.A., 1988. Late Proterozoic-Early Paleozoic of South America - - a collisional history. Episodes 11, 168-174. Ringwood, A.E., 1979. Origin of the Earth and Moon. SpringerVerlag, New York.
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Sautter, V., Harte, B., 1988. Diffusion gradients in an eclogite xenolith from the Roberts Victor Kimberlite Pipe: 1. Mechanism and evolution of garnet exsolution in AlzO3-rich clinopyroxene. J. Petrol. 29, 1325-1352. Selverstone, J., Stern, C.R., 1983. Petrochemistry and recrystallization history of granulite xenoliths from the Pali-Aike volcanic field, Chile. Am. Mineral. 68, 1102-1112. Skewes, M.A., Stern, C.R., 1979. Petrology and geochemistry of alkali basalts and ultramafic inclusions from the Pali-Aike volcanic field in southern Chile and the origin of the Patagonian plateau lavas. J. Volcanol. Geotherm. Res. 6, 3-25. Stern, C.R., Kilian, R., 1996. Role of the subducted slab, mantle wedge and continental crust in the generation of adakites from the Andean Austral Volcanic Zone. Contrib. Mineral. Petrol. 123, 263-281. Stern, C.R., Futa, K., Saul, S., Skewes, M.A., 1986. Nature and evolution of the subcontinental mantle lithosphere below southern South America and implications for Andean magma genesis. Rev. Geol. Chile 27, 41-53. Stern, C.R., Saul, S., Skewes, M.A., Futa, K., 1989. Garnet peridotite xenoliths from Pali-Aike basalts of southernmost South America. Kimberlites and related rocks. Geol. Soc. Aust., Spec. Publ. 14. Blackwell, Carlton, Australia, pp. 735744. Stern, C.R., Frey, F.A., Futa, K., Zartman, R.E., Peng, Z., Kyser, T.K., 1990. Trace-element and Sr, Nd, Pb, and O isotopic compositions of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America. Contrib. Mineral. Petrol. 104, 294-308. Taylor, S.R., McLennan, S.M., 1985. The Continental Crust: Its Composition and Evolution. Blackwell, Oxford. Taylor, R.P., Jackson, S.E., Longerich, H.P., Webster, J.D., 1996. In situ trace element analysis of individual silicate melt inclusions by laser ablation microprobe-inductively coupled plasma-mass spectrometry (LAM-ICP-MS). Geochim. Cosmochim. Acta 61, 2559-2567. Walker, R.J., Carlson, R.W., Shirey, S.B., Boyd, F.R., 1989. Os, Sr, Nd and Pb isotope systematics of southern African peridotite xenoliths: implications for the chemical evolution of the subcontinental mantle. Geochim. Cosmochim. Acta 53, 15831595. Webb, S.A.C., Wood, B.J., 1986. Spinel-pyroxene-garnet relationships and their dependence on Cr/A1 ratio. Contrib. Mineral. Petrol. 92, 471-480. Wells, P.R.A., 1977. Pyroxene thermometry in simple and complex systems. Contrib. Mineral. Petrol. 62, 19-139. Werling, F., Altherr, R., 1997. Thermal evolution of the lithosphere beneath the French Massif Central as deduced from geothermobarometry on mantle xenoliths. Tectonophysics 275, 119-141. Witt-Eickschen, G., Seck, H.A., 1991. Solubility of CaO and A120 3 in orthopyroxene from spinel peridotite: an improved version of an empirical geothermometer. Contrib. Mineral. Petrol. 106, 431-439.
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LITHOS ELSEVIER
Lithos 48 (1999) 237-262
Erosion of lithospheric mantle beneath the East African Rift system" geochemical evidence from the Kivu volcanic province Tanya Furman a,,, David Graham
b
a Department of Geosciences, The Pennsylvania State University, University Park, PA 16802, USA b College of Oceanic and Atmospheric Sciences, Oregon State University, Corvallis, OR 97331, USA
Received 20 April 1998; received in revised form 9 February 1999; accepted 10 February 1999
Abstract This study presents new major and trace element and Sr-Nd isotopic results for a suite of Miocene-Recent mafic lavas from the Kivu volcanic province in the western branch of the East African Rift. These lavas exhibit a very wide range in chemical and isotopic characteristics, due to a lithospheric mantle source region that is heterogeneous on a small scale, probably < 1 kin. The chemical and isotopic variations are mostly geographically controlled: lavas from Tshibinda volcano, which lies on a rift border fault on the northwestern margin of the province, have higher values of 87Sr/86Sr, (La/Sm) n, Ba/Nb, and Z r / H f than the majority of Kivu (Bukavu) samples. The range of 87Sr/86Sr at Tshibinda (0.70511-0.70514) overlaps some compositions found in the neighboring Virunga province, while Bukavu group lavas include the lowest 87Sr/86Sr (0.70314) and highest ~Nd ( + 7.6) yet measured in western rift lavas. The Tshibinda compositions trend towards a convergence for Sr-Nd-Pb isotopic values among western rift lavas. Among Kivu lavas, variations in 143Nd/144Nd correlate with those for certain incompatible trace element ratios (e.g., Th/Nb, Zr/Hf, La/Nb, Ba/Rb), with Tshibinda samples defining one compositional extreme. There are covariations of isotopic and trace element ratios in mafic lavas of the East African Rift system that vary systematically with geographic location. The lavas represent a magmatic sampling of variations in the underlying continental lithospheric mantle, and it appears that a common lithospheric mantle (CLM) source is present beneath much of the East African Rift system. This source contains minor amphibole and phlogopite, probably due to widespread metasomatic events between 500 and 1000 Ma. Lava suites which do not show a strong component of the CLM source, and for which the chemical constraints also suggest the shallowest magma formation depths, are the Bukavu group lavas from Kivu and basanites from Hurl Hills, Kenya. The inferred extent of lithospheric erosion therefore appears to be significant only beneath these two areas, which is generally consistent with lithospheric thickness variations estimated from gravity and seismic studies. 9 1999 Elsevier Science B.V. All rights reserved. Keywords: East African Rift system; Kivu volcanic province; Lithospheric mantle; Basalt geochemistry; Continental rifting
1. Introduction The subcontinental lithospheric mantle (SCLM) comprises the basal part of the Earth's outer rigid mechanical boundary layer, and may also represent a
* Corresponding author
chemical a n d / o r thermal boundary layer in the shallowest mantle (Harry and Leeman, 1995). The S C L M can contain old portions of mantle with distinctive trace element and isotope characteristics, due to prolonged isolation from underlying asthenospheric convection (McDonough, 1990). It is thought to have originated and evolved as a residue of ancient partial
0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All fights reserved. PII: S0024-4937(99)00031-6
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T. Furman, D. Graham/Lithos 48 (1999) 237-262
melting followed by the polybaric crystallization of silicate melts and hydrous fluids (Hawkesworth et al., 1990). Direct evidence on its composition comes from mantle xenoliths entrained in continental lavas. The small size and limited spatial distribution of xenoliths, however, may not provide an accurate representation of regional variations in the composition of the SCLM. Continental volcanic rocks, particularly silica-undersaturated mafic lavas, may be especially useful for this purpose. Such lavas are often taken to represent partial melts of the SCLM, formed either above a thermal anomaly such as a mantle plume, or during tectonic extension and associated continental rifting. In this study, we investigate the geochemistry of Miocene to Recent mafic lavas from the Kivu volcanic province, located in the western branch of the East African Rift, in order to document changes in melt composition associated with lithospheric thinning above a hypothesized mantle plume. We interpret the extreme heterogeneity in isotopic and incompatible trace element abundance ratios found in Kivu lavas to be indicative of dramatic changes in mantle source composition following the onset of volcanism near 12 Ma. By comparing the trace element and isotopic results from Kivu with earlier studies from throughout the eastern and western rift branches, we find evidence for a common lithospheric mantle (CLM) source that has been sampled by lavas over an area of approximately 106 km 2. The mineralogy of this common source includes minor amphibole and phlogopite, and may be similar in composition to the oceanic lithospheric mantle described by Class and Goldstein (1997). In the East African Rift system, variations in the inferred relative abundances of hydrous phases (amphibole and phlogopite) in the mantle source are also related to Sr and Nd isotopic differences, consistent with a multistage metasomatic history for the continental lithospheric mantle in this region.
2. Background
2.1. Geodynamic setting of the East African Rift system The East African Rift system (Fig. 1) traverses two regions of topographic uplift, the Ethiopian and
Kenyan domes, separated by a zone of N W - S E trending extension (Anza graben). A second N W - S E trending rift that includes Lakes Tanganyika, Rukwa and Malawi defines the southern extent of the Kenyan dome. Between these borders, the rift system comprises two branches, separated by the ~ 1300 kmwide East African plateau. The Kenyan dome is believed to overlie an upwelling plume head that has begun to flatten beneath the continental lithosphere (White and McKenzie, 1989; Griffiths and Campbell, 1991). Detailed geophysical work both along the rift axes and across the East African plateau has helped reveal some of the dynamics of plume encroachment. Recent profiles (summarized in Simiyu and Keller, 1997) indicate a broad (1200 _+ 100 km wide) negative gravity anomaly associated with the Kenya dome that extends westward to Lakes Edward and Kivu and southeastward into Tanzania. The regional gravity study of Ebinger et al. (1989) found that topographic wavelengths > 1000 km are overcompensated across the Kenyan dome, suggesting that surface features are maintained by dynamic uplift from the upper mantle. Taken together, these observations suggest that a hot mantle plume is centered beneath the northern part of the Tanzanian craton and Lake Victoria, and model calculations are consistent with a plume head diameter of 600 km (Simiyu and Keller, 1997). Superposed on the gravity signature of the plateau are narrow, steep-sided negative anomalies that define the boundary between Proterozoic orogenic belts and the Archean Tanzanian craton and that are coincident with the rift valleys themselves (Simiyu and Keller, 1997). Detailed gravity studies (Upcott et al., 1996; Simiyu and Keller, 1997) suggest that the underlying mantle plume has two arms with diameters < 250 km that penetrate the lithosphere to shallow levels beneath the eastern and western rift branches. The gravity anomaly associated with the eastern rift is shallowest beneath north central Kenya and deepens rapidly to the north and south (Simiyu and Keller, 1997). In the western rift, the geophysical data suggest that the greatest extent of lithospheric thinning has occurred just south of the Kivu volcanic province. Experimental investigations of plume dynamics (Griffiths and Campbell, 1991) also suggest that the narrow, arcuate western rift may
239
T. Furman, D. Graham/Lithos 48 (1999) 237-262
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Fig. 1. Map of the East African Rift system. Insets show locations discussed in the text. Areas of Miocene to Recent volcanism are shaded. Inset (A): eastern branch. Centers of mafic silicate volcanism mentioned in the text are indicated by filled circles, carbonatite localities are indicated by open circles. Filled triangles are major off-rift volcanic edifices. Inset (B): sketch maps of the Kivu and Virunga volcanic provinces, with areas of post-Miocene volcanism shaded. Volcanic centers are indicated by filled triangles, and smaller vents by filled circles. Key to Kivu sample localities: Bug - - N. Bugarama; Buk - - Bukavu; Gis - - Gisakura; Kak - - Kakondo; Kat - - Katana; Ley Leymera; Mbr - - Mbirizi; Ntd - - Ntode River; Ruh Ruhagarika; Shn Shangazi River. Key to Virunga vents: Gma - - Goma; Bsh Bushwaga; Muk - - Mukuvu; Bus - - Busamba; Mug - - Muganza.
reflect subsidence of cold lithospheric mantle near the edge of a plume head. This model is consistent
with the low degree of extension estimated for the western rift ( < 15%; Ebinger, 1989b), and may be
240
T. Furman, D. Graham/Lithos 48 (1999) 237-262
appropriate for parts of the eastern rift as well. Under this scenario, the post-Miocene alkalic volcanism
throughout the East African Rift system is primarily caused by melting of lithospheric mantle.
Table 1 Major and trace element analyses of Kivu lavas Sample prefixes: B = Burundi, R = Rwanda, Z = Zaire (Congo). Major and selected trace elements (Rb, Sr, Ba, Zn, Ni, V, Y, Nb, Zr, La, Ce) were determined by X-ray fluorescence (XRF) on fused disks (major elements) and pressed powder pellets (trace elements) at the University of Massachusetts (Amherst). Instrumental neutron activation analyses for the REE, Co, Cr, Hf, Sc, Ta, Th were performed on splits of the same samples at the Massachusetts Institute of Technology. Where only La and Ce are reported, these values were analyzed by XRF; when all REE are reported, the INAA values are used for La and Ce. One-sigma precision estimates for XRF and INAA based on replicate analyses are: major elements (except MnO) < 1%; La, Cr, Co, Hf, Sc, Ba, Rb, y, Sr, Ni, V, Zn, Zr < 2%; remaining REE, Nb, Ta, MnO 2-5%; Tb, Th 5-10%. Sample
Unit
Location
SiO 2
TiO 2
B 10C R3L R5N R2J R6C R4HA R3K R4Q R5A1 R5A3 Z6G Z4H1 Z7Z Z6A Z6B Z3C1 Z3C2 Z3D Z5G
Tv2 Tvl Qv Tv2 Tv2 Tv Tvl Tv Tv Tv Tv Tv Qv Tvl Tvl Qv Qv Qv Qv
Ruhagarika Bugarama Gisakura Mbirizi Mbirizi Mbirizi Ntode R. Shangazi R. Shangazi R. Shangazi R. Kakondo Katana Leymera NW Bukavu NW Bukavu Tshibinda Tshibinda Tshibinda Tshibinda
50.00 44.89 45.85 48.24 44.63 45.31 51.42 45.27 45.79 45.35 46.99 49.35 46.60 46.56 46.74 46.63 46.21 46.10 46.49
1.90 2.91 2.54 2.33 2.20 2.26 2.16 2.26 2.21 2.24 1.54 1.43 1.93 1.99 1.99 1.49 1.49 1.50 1.53
Sample
Unit
Location
Rb
Cs
B10C R3L R5N R2J R6C R4HA R3K R4Q R5A1 R5A3 Z6G Z4H1 Z7Z Z6A Z6B Z3C1 Z3C2 Z3D Z5G
Tv2 Tvl Qv Tv2 Tv2 Tv Tvl Tv Tv Tv Tv Tv Qv Tvl Tvl Qv Qv Qv Qv
Ruhagarika Bugarama Gisakura Mbirizi Mbirizi Mbirizi Ntode R. Shangazi R. Shangazi R. Shangazi R. Kakondo Katana Leymera NW Bukavu NW Bukavu Tshibinda Tshibinda Tshibinda Tshibinda
15 36 34 46 35 30 33 28 27 31 23 16 31 36 35 55 47 52 66
0.14 0.38 0.39 0.47 0.2 bdl 0.14 0.3 0.35 0.66 0.51 -
A1203
Fe 20 3
MnO
MgO
CaO
Na 20
K 2O
14.16 14.26 14.58 15.51 14.62 13.28 16.61 12.95 13.44 13.33 14.96 16.05 15.55 14.63 14.61 14.18 14.05 14.02 14.35
11.89 12.88 12.08 10.31 11.43 11.88 12.56 11.82 11.86 11.75 12.60 10.93 11.85 10.78 10.85 11.41 11.32 11.05 11.27
0.19 0.21 0.25 0.17 0.22 0.20 0.13 0.20 0.20 0.20 0.20 0.16 0.23 0.20 0.20 0.19 0.20 0.19 0.20
6.70 8.93 9.09 8.07 10.07 11.37 4.90 11.94 10.95 11.24 9.28 7.19 8.69 8.27 8.72 9.10 8.83 8.74 8.76
11.50 10.17 10.21 9.36 11.53 11.70 6.77 11.52 11.30 11.32 10.76 10.02 10.55 11.20 10.92 11.92 12.15 12.11 12.47
2.74 3.44 3.43 3.25 3.14 2.28 3.17 2.74 2.68 2.96 2.48 3.29 3.17 3.77 3.52 3.21 2.99 3.61 2.99
0.49 1.35 1.23 1.89 1.15 1.04 1.51 0.52 1.05 1.11 0.80 0.83 1.03 1.42 1.39 1.03 1.57 1.55 0.94
Sc
V
Cr
Co
Ni
Zn
24.0 23.4 21.0 . . 30.1 . 29.8 23.2 26.8 22.0 22.6 28.4 28.4 -
173 212 218 192
245 221 255 216 . . 237 442 . 411 355 206 267 304 304 315 309 305 284
46.3 52.1 46.8
147 143 182 144
115 110 101 94.9
58.7
187 268
124 99.4
63.3 46.5 60.5 45.5 53.3 55.7 53.8 -
248 218 115 146 162 171 187 171 151 172
98.5 103 91.0 88.0 89.9 91.6 94.0 91.6 85.4 102
Sr
Ba
353 727 688 768 667 652 401 585 768 587 460 623 710 1247 1198 737 821 867 898
230 577 654 701 . . 767 536 . 611 536 783 718 1014 977 768 1175 1310 1235
. .
. . 135 241
.
. 228 230 175 207 189 188 208 193 203 186
. .
.
T. Furman, D. Graham / Lithns 48 (19991 237-262
western rift ca. 12 Ma (Bellon and Pouclet, 1980; Kampunzu et al., 1986; Ebinger, 1989a; Pasteels et
Volcanism and uplift began roughly contemporaneously in the eastern rift ca. 23 Ma, and in the
P,O,
Total
Mg#
0.29 0.94 0.62 0.63 0.76 0.56 0.50 0.55 0.51 0.54 0.37 0.49 0.65 0.90 0.90 0.66 0.79 0.78 0.82
99.86 99.99 99.88 99.76 99.75 99.88 99.73 99.76 99.98 100.04 99.98 99.74 100.25 99.72 99.83 99.8 1 99.59 99.65 99.82
56.75 61.77 63.66 64.54 67.19 69.02 47.60 70.15 68.27 69.04 63.19 60.48 63.15 64.09 65.17 65.00 64.42 64.77 64.40
Y
Zr
Nb
€If
Ta
Th
U
Pb
26 35 31 29 31 28 76 28 27 29 31 25 29 29 30 27 27 27 28
132 290 247 283
29.1 65.4 70.3 79.4
3.0 5.8
1.1
-
-
2 2 3
3
3.2
5.9
3.8
-
-
-
-
-
-
4.1 4.2 7.0 5.5 7.0 6.0 6.0 6.8 6.0 7.0 6.0 10.2 7.7 11.3 10.4 12.0 13.8 12.8 14.0
-
-
219 191 -
203 122 127 207 241 235 144 155 143 160
58.3 72.1
4.0
3.3
-
-
-
70.1 56.0 63.7 95.2 124 122 87.3 99.6 98.6 103
4.1
3.3
-
-
2.5 4.4 4.3 4.3
2.5 4.3 5.5 5.0 ~
~
3.1 3.3
4.3 4.2
-
-
2
3 2 2 2 2 3
I 3 2 6 6 3 4 4 3
4 5
4 5 3 4 3 5 5 5 6 4 5 6 5 6 7 5
24 1
La
24.8 44.8 52.1 45.2 -
Ce
49.7 93.0 93.7 91.7
Nd
20.0 44.9 -
Eu
Tb
Yb
Lu
4.69 9.72
1.57 3.15
0.81 1.31
2.16 2.69
0.30 0.40
-
-
-
-
-
8.03
2.50
1.00
2.53
0.33
-
-
-
Sm
38.9
-
-
-
-
-
-
-
-
-
17 49.0
99.0 95.6
40.1
-
-
-
49.2 41.3 59.9 60.4 94.7 93.2 70.0 76.7 77.3 86.7
98.0 68.8 102 114 179 173 117 133 132 138
40.6 -
32.8 39.0 63.9 61.5 ~
7.88
2.37
1.01
2.43
0.33
-
-
-
-
-
7.82
2.35
1.03
2.41
0.33
-
-
-
-
-
1.74 2.21 2.88 2.95
0.83 0.92 1.08 1.09
2.10 2.87 2.35 2.37
0.32 0.40 0.30 0.36
-
-
0.95 0.95
2.48 2.75
0.39 0.37
-
-
-
5.44 6.91 10.2 10.0 ~
1
7.79 7.61
47.0 44.3 -
-
2.20 2.22 1
~
1
242
T. Furman, D. Graham/Lithos 48 (1999) 237-262
al., 1989). Mid-Miocene to Recent volcanic activity has occurred along the entire length of the eastern rift, but is restricted to four intrabasinal accommodation zones in the western rift (Ebinger, 1989a,b; Fig. 1). The diversity of mafic volcanic rocks erupted along the eastern and western branches of the rift system has been well-documented (e.g., Holmes and Harwood, 1937; Holmes, 1940, 1950; Bell and Powell, 1969; Bell and Doyle, 1971; Mitchell and Bell, 1976; Baker et al., 1977; De Mulder et al., 1986; Auchapt et al., 1987; Davies and Lloyd, 1989; Marcelot et al., 1989; Lloyd et al., 1991; Rogers et al., 1992, 1998; Class et al., 1994; Furman and Graham, 1994; Furman, 1995; Paslick et al., 1995), and can be used to investigate the interaction between magmas derived from asthenospheric and lithospheric sources beneath this region of the African plate.
2.2. The Kivu volcanic province The Kivu volcanic province is located in the western branch of the East African Rift, along the borders of Rwanda, Burundi and eastern Zaire (Congo). It includes two discrete volcanic fields: Bukavu, which covers an area roughly 35 • 35 km 2 near Lake Kivu, and Mwenga-Kamituga, located 80 km to the southwest. Samples from this study come from Bukavu and include four lavas from Tshibinda volcano (Fig. 1). The Kivu area comprises three sedimentary basins defined by border faults, and its volcanism is intimately linked to faulting during basin formation (Ebinger, 1989a). Three cycles of volcanic activity have been recognized at Bukavu (Kampunzu et al., 1986; Ebinger, 1989a; Pasteels et al., 1989), each of which is dominated by fissure eruptions of mafic lavas. Earliest activity (unit T v l ) occurred prior to rifting, between roughly 10 and 7.5 Ma and is limited to the East Kivu basin and the southern part of Idjwi Island. Mafic lavas from this period include olivine- and quartz-normative tholeiites. Second-stage volcanism (unit Tv2), which likely corresponds to the start of rift formation, occurred between ~ 7.5 and 4 Ma in both the East and West Kivu basins. Lavas erupted along the rift boundary faults during this episode include sodic alkali basalts and basanites in addition to minor volumes of trachytes and phonolites. The
third stage of volcanic activity (Qv) includes tholeiitic and alkalic basalts erupted primarily along the West Kivu border fault system. Tshibinda volcano is one of the most recently active volcanic centers located on this fault. The West Kivu border fault has served as the master fault for crustal extension during the Quaternary, and forms a structural link between the Kivu and Virunga provinces (Ebinger, 1989a). Samples for this study are mafic lavas from each eruptive cycle (Table 1). Samples from Tshibinda Table 2 Sr and Nd isotope results for Kivu volcanic province lavas th = tholeiite, ab = alkali basalt. Sr and Nd isotope analyses were performed at the University of California (Santa Barbara) on a Finnegan MAT 261 multicollector mass spectrometer, operated in static mode for Sr and in dynamic mode for Nd. Sr was normalized within-run to 86Sr/88 Sr = 0.1194, and adjusted to a value of 0.710250 for NBS 987 (the mean value measured during the course of the study was 0.710199). Nd was normalized within-run to 146Nd/144Nd=0.721900. The mean value measured for the Ames Nd standard during the course of the study was 0.511890. In addition, 143Nd/144Nd ratios measured for two separate dissolutions of BCR-1 were 0.512640 and 0.512629. Chemical separations followed procedures outlined in (Hoernle, 1990). Briefly, approximately 100 mg of whole rock powder was leached in 2 N HC1 for 1 h at 50~ then rinsed several times with ultrapure distilled water; prior to overnight dissolution in HF + HC104, Sr and Nd were sequentially separated by a series of ion-exchange chromatography columns. Blanks for Sr and Nd were ~0.3 and < 1 ng, respectively, which is insignificant for the samples studied here. Location Sample Type 87/868r -k- 143/144Nd • end Ruhagarika N Bugarama Gisakura Mbirizi Mbirizi Mbirizi Ntode R. Shangazi R. Shangazi R. Shangazi R. Kakondo Katana NW Bukavu NW Bukavu Leymera Tshibinda Tshibinda Tshibinda Tshibinda
B10C R3L R5N R2J R6C R4HA R3K R4Q R5A1 R5A3 Z6G Z4H 1 Z6A Z6B Z7Z Z3C1 Z3C2 Z3D Z5G
th ab ab ab ab ab ab ab ab ab ab th ab ab ab ab ab ab ab
0.704409 0.703138 0.703493 0.703816 0.703575 0.703999 0.704931 0.703930 0.704234 0.704037 0.704567 0.704365 0.703994 0.703987 0.703429 0.705106 0.705165 0.705108 0.705138
8 9 8 9 10 12 11 9 12 9 8 9 11 10 12 11 10 12 11
0.512838 0.513026 0.512925 0.512907 0.512888 0.512870 0.512749 0.512871 0.512841 0.512851 0.512777 0.512751 0.512815 0.512775 0.512899 0.512669 0.512671 0.512659 0.512660
6 7 7 5 6 5 5 6 8 7 8 7 6 6 10 7 5 6 8
3.90 7.57 5.60 5.25 4.88 4.53 2.17 4.55 3.96 4.15 2.71 2.20 3.45 2.67 5.09 0.60 0.64 0.41 0.43
243
T. Furman, D. Graham/Lithos 48 (1999) 237-262
volcano and Idjwi Island (Marcelot et al., 1989) are considered together as the "Tshibinda group", while remaining lavas are termed the "Bukavu group". All lavas contain phenocrysts of olivine and clinopyroxene, with plagioclase feldspar phenocrysts restricted to evolved mafic lavas (Appendix A). The samples were collected by C.J. Ebinger (Leeds, UK) and were analyzed for major and trace elements (Table 1) as well as Sr and Nd isotope ratios (Table 2).
Na20 not shown) do not define coherent trends against MgO. Furthermore, CaO/A1203 values for lavas with 7-12 wt.% MgO range from 0.62 to 0.89, but values of ~ 0.8 are found at all MgO contents within this range (Fig. 2). Four alkali basalts from Tshibinda volcano have nearly uniform compositions ( ~ 9 wt.% MgO). Abundances of compatible trace elements indicate that most lavas in this series have fractionated olivine and/or clinopyroxene. The Ni, Cr and Sc contents of lavas with 11-13 wt.% MgO are close to values typical of mantle-derived basalts (Table 1). Abundances of Ni (Fig. 2), Cr and V decrease with decreasing MgO content, while Sc shows no regular variation with MgO or C a O / A1203.
2.3. Results 2.3.1. Major and compatible trace elements The major element variations of Kivu lavas indicate that this lava series cannot be related through fractional crystallization from a common parent. This is supported by the observation that most major element oxides (e.g., P205, Fig. 2; also TiO 2, K 2 0 ,
2.3.2. Incompatible trace elements Incompatible trace element abundances in Kivu lavas (e.g., La; Fig. 2) are not correlated with MgO
1.25
1.25
I
A
1.00
B -
1.00
9
tt'3
c',.I r.,,-i
0.75
9
,r
t"q r 0.50
- 0.75 9
9
0.25
9
Bukavu group
- 0.50 ~
Tshibinda group 0.00
I
I
I
I
I
I
I
O.25
I
D
C
Idjwi Island
250
100 o~,.~
%
200
,...]
Z
5O
ii,
.r
150 100 4
J
i
t
i
6
8
10
12
MgO
4
I
I
I
i
6
8
10
12
0
14
MgO
Fig. 2. Variations in major and trace elements among Kivu mafic lavas. Filled diamonds are samples from Rwanda and Burundi (Bukavu group), and crossed diamonds are samples from Tshibinda volcano and Idjwi Island (Tshibinda group). Data are from this study and from Marcelot et al. (1989). (A) Abundances of 1'205 show no consistent trend with decreasing MgO, indicating the lavas cannot be derived by closed-system fractionation of a single parental mafic magma. (B) Values of C a O / A I 2 0 3 show little variation among samples with 7-12 wt.% MgO. (C) Abundances of compatible elements such as Ni decrease with decreasing MgO content of Kivu mafic lavas, indicating progressive removal of olivine and/or clinopyroxene. (D) Abundances of incompatible elements such as La increase broadly with decreasing MgO, but the high degree of scatter precludes simple differentiation processes. The primitive alkali basalt from Idjwi Island (sample LKA-4 of Marcelot et al., 1989) has unusually high abundances of most incompatible trace elements.
244
T. Furman, D. Graham/Lithos 48 (1999) 237-262
content. This observation was also made by Marcelot et al. (1989) based on a smaller dataset. The abundances of several incompatible trace elements do correlate strongly with one another. Values of S r / C e (Fig. 3) and P / C e are uniform and fall within the range expected for mantle-derived basalts [mean P / C e value 56.7 _+ 5.9, with two outliers, RW88 (Marcelot et al., 1989) and R3L, both from Bugarama and possibly from the same unit, between 102 and 104]. Large ion lithophile elements (LILE; Ba, Rb, Sr) are correlated with one another but not with Th or the high field strength elements (HFSE). Variations between Th, Nb and Zr are geographically controlled (Fig. 3): lavas from the Tshibinda group have higher T h / N b and N b / Z r than lavas from the Bukavu group. A similar pattern is found for B a / L a and Ba/Nb, both of which are elevated among Tshibinda group samples.
Chondrite-normalized rare earth element (REE) patterns of Kivu mafic lavas are not parallel (Fig. 4). Highly variable MREE contents lead to crossing patterns that require derivation of the lavas from heterogeneous (or different) mantle sources. Values of (La/Sm) n are not correlated with La abundances, whereas (La/Yb), values are positively correlated with La content (Fig. 5). Lavas from the Tshibinda group have higher ( L a / S m ) , than lavas from the Bukavu group (Fig. 5), but crossing REE patterns occur within the latter group as well.
2.3.3. Sr-Nd isotopes Values o f 878r/86Sr a n d 143Nd/144Nd show a strong negative correlation among Kivu lavas (Fig. 6). The range of isotopic ratios is unusually large for such a small area, and requires short-range isotopic
2000
20
A
B
1500 -
-
** ~
Z4H1
1000 -
[
500 -
@
Bukavu group
' ~
t.
- 10 [-~
O
-
0 0
50
100
150
200
250
0
C 150
-
100
-
i
50
100
150
200
Nb
Ce
200
,-~
5
Tshibinda group
0
Z
15
i
i
50-
0 100
I
I
I
150
200
250
300
Zr Fig. 3. Incompatible element-element diagrams for Kivu mafic lavas. (A) Sr vs. Ce. Sr and Ce are positively correlated among all Kivu samples with an average S r / C e ratios of 6.5, within the range for ocean island basalts but higher than primitive mantle estimates (12; Sun and McDonough, 1989). (B) Th vs. Nb. Th and Nb are positively correlated among Kivu lavas, but samples from the Tshibinda group have higher T h / N b values (0.14) than samples from the Bukavu group (0.09). The estimated primitive mantle T h / N b ratio is 0.12 (Sun and McDonough, 1989). (C) Nb vs. Zr. Relative abundances of Nb and Zr show wide variation within the Kivu province, but samples from the Tshibinda group have generally higher Nb at given Zr values than lavas from the Bukavu group.
245
T. Furman, D. Graham/Lithos 48 (1999) 237-262
B10C
--
(D
R2J
-
R3L
,-~
Z3D
1000 ,-~
Z4Z1
10-
KIVU PROVINCE La Ce
Nd
Sm Eu
Tb
Yb Lu
Fig. 4. Chondrite-normalized REE patterns for Kivu mafic lavas. The REE patterns are not parallel, and show large variations in MREE abundances. heterogeneity in the mantle beneath this region. Four Quaternary lavas from Tshibinda volcano have the highest 87Sr/86Sr values (0.70511-0.70514) and lowest eNd (0.41-0.64). The uniform isotopic values measured at Tshibinda contrast with the wide ranges recorded in other parts of the volcanic province. Lavas from the earliest phase of mafic volcanism in
A 6 r.~
5
'~
4
It
the Kivu Bukavu group have 87Sr/86Sr values between 0.70314 and 0.70493 and eNd between 2.17 and 7.57 (Fig. 6). The 13 remaining lavas, of all ages and from throughout the Kivu area, fall within this isotopic range and do not show a consistent geographic variation. Several ratios of incompatible trace element abundances correlate negatively with Nd isotopic values (e.g., T h / N b , L a / N b , B a / N b ) , suggesting that they like Sr isotopic ratios are a feature of the mantle source region and vary over short distances. In each case, lavas from Tshibinda form an endmember in the Kivu suite. 0.5131
9
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9
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Tshibinda 0.5126 0.7030
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100
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La Fig. 5. (A) (La/Sm) n vs. La abundance for Kivu mafic lavas. (B) (La/Yb)n vs. La. The large variations in MREE abundances are manifest in a narrow range in LREE/MREE ratios that do not vary with La content, but values of LREE/HREE that are positively correlated with La abundances.
I
I
I
I
0.7035
0.7040
0.7045
0.7050
0.7055
S7Sr/86Sr Fig. 6. 87sr/g6sr vs. 143Nd/144Nd for Kivu mafic lavas. Sr and Nd isotopes are negatively correlated among all Kivu lavas. Samples from Tshibinda (circled) have a restricted compositional range, while samples from the remainder of the Kivu province show a high degree of variability. Sample B 10C from Burundi is indicated by an open square.
246
T. Furman, D. Graham/Lithos 48 (1999) 237-262
3. Discussion
3.1. Major element characteristics of mafic rift lavas The eastern and western branches of the rift system are characterized by differences in the timing, volume and chemical composition of erupted lavas. In the eastern rift, volcanism began at roughly 23 Ma and the total erupted volume is estimated at 220,000 km 3 (Williams, 1972). The Kenya rift volcanics erupted nearly continuously from Early Miocene to Holocene time (Baker et al., 1971). In general, the Kenya basalts are weakly undersaturated with respect to silica. Erupted compositions considered in this study include tholeiites, ferrobasalts and alkali basalts from O1 Tepesi and Naivasha in central Kenya (Baker et al., 1977; Davies and Macdonald, 1987), and alkali basalts and basanites from Huri Hills in northern Kenya (Class et al., 1994). Lavas from northern Tanzania (Paslick et al., 1995) are dominated by mildly alkalic compositions and include samples from several volcanic vents that date from > 8 Ma to Recent. Volcanism in the western rift began at roughly 12 Ma and has produced at most 100,000 km 3 of lava (Kampunzu and Mohr, 1991). Eruptions have been restricted to four volcanic provinces (Fig. 1) located in heavily faulted intrabasinal accommodation zones (e.g., Ebinger, 1989a,b). Mafic lavas from the western rift are undersaturated with respect to silica, although the nature and degree of alkali enrichment vary greatly both within and between volcanic provinces. Toro Ankole is dominated by ultrapotassic lavas and other highly alkaline compositions, including pyroclastic carbonatites (e.g., Holmes and Harwood, 1937; Lloyd and Bailey, 1975; Lloyd et al., 1991). The Virunga lavas are mildly to highly undersaturated, with compositions ranging from alkali basalts to K-rich (ultrapotassic) basanites (Holmes and Harwood, 1937; De Mulder et al., 1986; Marcelot et al., 1989; Rogers et al., 1992, 1998). Kivu province lavas are similar to eastern rift compositions, including alkali basalts and the only tholeiitic lavas sampled in the western rift (Kampunzu et al., 1986; Auchapt et al., 1987; Marcelot et al., 1989). To the south, Rungwe lavas include alkali basalts, basanites, nephelinites, as well as the only
trachy-phonolitic central volcanoes in the western rift (Harkin, 1960; Furman, 1995). In the following discussion, we consider lavas from each of these volcanic provinces.
3.2. REE characteristics of mafic rift lavas We begin with the REE because the composition of mantle peridotite can be used as a well-defined reference point, and because REE behavior during melting is reasonably well-understood. Chondritenormalized diagrams for all volcanic provinces of the East African Rift system show LREE enrichments relative to HREE (Fig. 7). In most cases (e.g., Virunga province in the western rift and Naivasha and O1 Tepesi from the eastern rift), lavas from a single area have sub-parallel REE patterns that do not cross one another, and REE abundances that increase as MgO contents decrease. Lavas from Rungwe and the Katwe-Kikorongo field of Toro Ankole in the western rift, plus Huri Hills in the eastern rift, display minor heterogeneity indicated by a small number of REE patterns that vary primarily in their abundances of Tb through Lu. In contrast, lavas from the Kivu province are markedly heterogeneous in relative abundances of all the REE. Among mafic lavas from all volcanic areas, the degree of LREE-enrichment, and the overall steepness of the sloping REE patterns (Fig. 7) generally increase together, as well as increasing with degree of silica undersaturation. The range of (La/Sm) n values among basalts, alkali basalts and ferrobasalts from Naivasha, O1 Tepesi, and Huri Hills (2.2-3.5) is somewhat smaller than the range observed among Huri Hills basanites (3.0-4.5) or at any single western rift volcanic center. In the western rift (La/Sm)n values at Rungwe, Karisimbi and Muhavura overlap (4.0-5.5), while values at Nyiragongo (5.2-6.7) and Toro-Ankole (6.0-6.7) are markedly higher. Notably, lavas from the Kivu province show the widest range in (La/Sm), values (3.0-7.0). In this province, basalts from the Bukavu group have similar values to the eastern rift (3.0-4.0), while lavas from the Tshibinda group have values similar to Nyiragongo and Toro-Ankole lavas (5.6-7.0). Lavas with relatively uniform (La/Sm)~ values from Kivu, Nyiragongo and Toro-Ankole have very different (La/Yb), values. Based on the extremely wide range
247
T. Furman, D. Graham / Lithos 48 (1999)237-262 1000
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Fig. 7. Chondrite-normalized abundances of REE (values of Boynton, 1983). Datasets were chosen on the basis of internal consistency when possible (data from same analytical facilities), and therefore do not include all available published data. Sources of data: Hurl Hills - - Class et al. (1994); N a i v a s h a - Davies and Macdonald (1987); O1Tepesi - - Baker et al. (1977); N. Tanzania - - Paslick et al. (1995); Muhavura Rogers et al. (1998); Karisimbi Rogers et al. (1992); Rungwe Furman (1995); Nyiragongo - - Marcelot et al. (1989), Furman (unpublished data); Toro Ankole - - Furman (unpublished data). (a) Eastern rift lavas. Ranges shown enclose the variation among mafic lavas from O1 Tepesi, Naivasha and Huri Hills. (b) Western rift I. The field for Karisimbi encompasses all primitive K-basanites. Two samples from Toro Ankole and one mafic lava from Nyamuragira were selected to indicate representative patterns in these areas. (c) Western rift II. Fields for Muhavura, Nyiragongo and Rungwe indicate the range of mafic lavas from each area.
T. Furman, D. Graham/Lithos 48 (1999) 237-262
248
in REE patterns, Mitchell and Bell (1976) concluded that the Toro-Ankole lavas, especially the ultra-alkaline ugandites, mafurites and katungites, could not be derived by a single-stage melting process from mantle peridotite, but require at least one earlier event of source enrichment. 3.3. Incompatible trace and minor element variations
Incompatible trace elements may give useful insight into the interaction between magmas derived
(a)
from asthenospheric and lithospheric sources. In particular, they can indicate the type of mantle involved (e.g., HIMU), the existence or extent of contamination by crust, the nature and degree of metasomatic enrichment events, and the source mineralogy when elements diagnostic of key phases such as apatite, zircon, or phlogopite are considered. All volcanic areas show enrichment in the highly incompatible elements relative to MORB and OIB, and the primitive-mantle normalized patterns (spidergrams) are not smooth (Fig. 8). Lavas from the
500
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100-
> "~ 9 ,,=,4
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~
1
-
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0.1 Cs Rb Ba Th Nb Ta K La Ce Sr P Nd Sm Zr Hf Eu Ti Tb Y Yb Lu 1000 Naivasha Recent Huff Hills 100 O1 Tepesi
"~ lO Naivasha II
E A S T E R N RIFT Cs Rb Ba Th Nb Ta K La Ce Sr P Nd Sm Zr Hf Eu Ti Tb Y Yb Lu Fig. 8. Primitive mantle normalized incompatible element variation diagrams for mafic rift volcanics (normalizing values of Sun and McDonough, 1989). See text for discussion. (a) Kivu province. Mafic lavas from the Tshibinda and Bukavu groups have distinct patterns; note particularly the differences in Ba-Th and K - L a between the two groups. One sample from Burundi has the lowest incompatible trace element abundances of all Kivu lavas. (b) Eastern rift lavas. Ranges shown enclose the variation among mafic lavas from O1 Tepesi and Huri Hills. Two representative samples from Naivasha indicate the distinct trace element abundances of mafic lavas from different ages a n d / o r eruptive centers. (c) Western rift I. The field for Karisimbi encompasses all primitive K-basanites. Two samples from Toro Ankole and one mafic lava from Nyamuragira were selected to indicate representative patterns in these areas. (d) Western rift II. Fields for Muhavura and Rungwe indicate the range of mafic lavas from these areas. One representative nephelinite from Nyiragongo is shown for comparison.
T. Furman, D. Graham/Lithos 48 (1999) 237-262
249
o
Toro Ankole 100 > o , , -. I 9 v.-,l
9 , . --i
"~
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K La Ce Sr
P Nd Sm Zr Hf Eu Ti Tb
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(d) ooo, .o.
Nyiragongo
100 -
Muhavura ',
10-
W E S T E R N R I F T II Cs Rb Ba Th Nb Ta K
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Fig. 8 (continued).
eastern rift display smoother overall spidergram patterns, and have lower incompatible trace element abundances, than those from the western rift. In general, lavas from a single area have parallel spidergrams; as discussed earlier, the Kivu province is exceptional in this regard. As expected on the basis of REE variations, lavas from all western rift volcanoes (except the Bukavu group from Kivu) show steep to concave-upward patterns from Ti to Lu (Fig. 8), with limited abundance ranges for these elements. Among eastern rift lavas, this pattern is seen only for the Hurl Hills basanites. This signature is indicative of melting in the presence of residual garnet, a phase in which these elements are compatible. Mafic rift lavas generally show no evidence of crustal contamination. These mafic lavas have unusually high abundances of incompatible trace elements which make them unlikely to be contaminated
easily during ascent or in crustal chambers. Detailed arguments regarding the lack of crustal assimilation have been made by several authors (e.g., Baker et al., 1977; Davies and Macdonald, 1987; Marcelot et al., 1989; Rogers et al., 1992, 1998; Class et al., 1994; Furman, 1995) and will not be presented here. As one example, values of S r / C e are within the range of ocean island basalts ( ~ 5-8) for lavas from all provinces in the western rift, and are slightly higher (9-12) in lavas from Huri Hills and Naivasha. Lavas that have assimilated continental crustal material should have elevated values of S r / C e and positive Eu anomalies resulting from incorporation of plagioclase feldspar. Rift lavas do not have these signatures, and thus the S r / C e values are characteristic features of their source regions. As similar arguments can be made for other individual elements, we infer that the incompatible trace element
250
T. Furman, D. Graham/Lithos 48 (1999) 237-262
features of mafic rift lavas have not been affected by crustal assimilation and can be used to fingerprint the source region.
3.3.1. Regional patterns of incompatible trace element enrichment There are key similarities throughout the rift system in the covariations of certain incompatible elements such as K, Ba, Rb, Th, Nb and La. Consistent geographic patterns of anomalous enrichment and depletion suggest that regional mineralogical heterogeneities in the underlying lithospheric mantle control the distribution of these anomalies in the erupted lavas. The most obvious feature of the spidergrams is the large negative potassium anomalies in lavas from Kivu (Bukavu group), Rungwe and Toro Ankole in the western rift, and from Naivasha in the eastern rift (Fig. 8). The degree of relative K depletion does not correlate with the level of incompatible trace element abundances (cf. Rungwe and Muhavura; Fig. 8) or with potassium content of the lavas (cf. Toro Ankole and Muhavura; Fig. 8). Relative potassium depletion is, however, correlated with Ba enrichment (Fig. 8). Ba enrichment is reflected in B a / R b values higher than the primitive mantle estimate of ~ 11 (Sun and McDonough, 1989) in samples from the Kivu Bukavu group, Toro Ankole, Rungwe, Nyamuragira, Nyiragongo and all eastern rift localities. Individual lavas from Rungwe, Naivasha, O1 Tepesi and Huri Hills have B a / R b values ranging from ~ 18 to over 100. Note that the Tshibinda group alkali basalts and ultrapotassic lavas from Karisimbi and Muhavura do not show Ba enrichment or K depletion. Covariation between Nb and Th illustrates the same regional pattern in trace element enrichment. Samples from the Kivu Tshibinda group, Karisimbi, and Muhavura have N b / T h values close to the estimated primitive mantle value of ~ 8 (Sun and McDonough, 1989). In contrast, samples from the Kivu Bukavu group, Rungwe, Toro Ankole, O1 Tepesi and Huri Hills have N b / T h values ~ 12, and indicate a higher compatibility for Th in the mantle source beneath these areas. Patterns of variation in B a / N b - L a / N b also suggest involvement of several source regions with distinct enrichment histories. Samples from the Kivu
Bukavu group and Toro Ankole have B a / N b ratios similar to primitive mantle estimates ( ~ 10; Sun and McDonough, 1989) but L a / N b ratios between 0.6 and 0.9, lower than primitive mantle values ( ~ 0.96; Fig. 9). In contrast, mafic lavas from the Kivu Tshibinda group and Muhavura have L a / N b ratios similar to primitive mantle but have higher B a / N b ratios (12-14). Huri Hills basanites have B a / N b L a / N b ratios that overlap the field of HIMU mantle inferred from ocean island basalt (Weaver, 1991; Fig. 9). Rungwe nephelinites and Karisimbi Kbasanites have large ranges in B a / N b and La/Nb, and form trends suggesting involvement of an enriched mantle (EMII) component, while alkali basalts from Rungwe and Naivasha are relatively enriched in Ba and trend towards EMI mantle. Alkali basalts from Huri Hills and O1 Tepesi are also enriched in Ba, and show increasing B a / N b ratios at constant L a / N b (Fig. 9). These variations are characteristic of enriched mantle reservoirs identified for OIB, but we suggest that they are present within the continental lithosphere as well.
3.3.2. Evidence for carbonatite metasomatism A diagnostic feature of metasomatized mantle is an increase in Z r / H f value (Dupuy et al., 1992; Rudnick et al., 1993), with values ranging between ~ 45 and 100. All rift samples have higher Z r / H f values than the primitive mantle ( ~ 36; Sun and McDonough, 1989): average Z r / H f values for Toro Ankole, Muhavura, Karisimbi and the eastern rift provinces range from 41-45. The elevated Z r / H f (and overall high trace element abundances) suggest that small-volume metasomatic fluids have enriched the source regions for every province. Lavas from the Kivu Tshibinda group, Rungwe and Nyiragongo have the highest Z r / H f values, with individual samples from these provinces between 60-83. These same regions show enrichment in REE relative to HFSE (e.g., Eu/Ti; Fig. 8). Both of these signatures are characteristic of carbonatite metasomatism (Dupuy et al., 1992; Rudnick et al., 1993) and suggest that the source areas for these mafic lavas were infiltrated by carbonate-rich magma. The geographic distribution of this source signature differs from that just described on the basis of other incompatible trace elements, and suggests that portions of
T. Furman,D. Graham/ Lithos 48 (1999)237-262
251
the lithosphere beneath the rift branches underwent more than one phase of metasomatic enrichment.
45
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3.4. Sr-Nd isotopic characteristics of East African Rift mafic lavas
Naivasha
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La/Nb Fig. 9. B a / N b against L a / N b for East African rift volcanics. (a) Eastern rift lavas have generally lower B a / N b and L a / N b values than primitive mantle estimates (Sun and McDonough, 1989), but each volcanic center includes samples with extremely high B a / N b values. Huri Hills basanites overlap estimates for HIMU (Weaver, 1991), consistent with their inferred plume source (Class et al., 1994). (b) Western rift lavas from the Tshibinda and Bukavu groups at Kivu have distinct ranges in B a / N b - L a / N b that indicate a sharp discontinuity in source composition between the two areas. Bukavu group samples overlap those from Toro Ankole and are depleted relative to primitive mantle estimates. Tshibinda group Kivu and Muhavura lavas, as well as individual samples from Rungwe and Karisimbi, have overlapping ranges in B a / N b L a / N b (10-14 and 0.8-0.9, respectively) that are similar to values observed at Naivasha. This range is interpreted to represent the range in the CLM source region. Primitive K-basanites from Karisimbi trend from the CLM source towards the EMII endmember, while Rungwe nephelinites trend towards EMI. Rungwe alkali basalts are enriched in Ba relative to associated nephelinites, probably due to an increased importance of amphibole melting in their mantle source region, and they trend towards the high values observed in the eastern rift.
In this section we focus on the Sr and Nd isotopes because these data provide constraints on mantle source compositions and they are available for a wide range of lava types from both rift branches. We begin by summarizing the Sr-Nd isotopic relations of East African carbonatites and associated undersaturated mafic lavas, because they are central to a comprehensive model of regional magnetism. The East African Carbonatite Line (EACL) was defined by Bell and B lenkinsop (1987) on the basis of Sr-Nd isotopic variations for young carbonatite lavas (Fig. 10). The principle carbonatite localities defining the EACL are eastern Uganda (Kisingiri, Napak, Tororo, Sukulu), western Uganda (Kalyango, Rusekere), northern Tanzania (Oldoinyo Lengai) and Kenya (Homa Bay). The EACL has been interpreted as a mixture between two mantle sources (Bell and Blenkinsop, 1987), with compositions similar to some ocean island basalt sources (Nelson et al., 1988), notably the HIMU (high U / P b ) and EMI (enriched mantle type 1) components (as described by Zindler and Hart, 1986). Diopsides from South African kimberlites (Menzies and Murthy, 1980) overlap the EACL at low end compositions and, notably, they form an extension of the array to much more enriched values (eNd = --13, 87Sr/S6Sr = 0.7075; Fig. 10). Although these kimberlites are located well outside the area of study for this paper, they demonstrate that the processes giving rise to the isotopic variations in the East African region are of general significance in the evolution of the SCLM. Recent isotopic studies at individual carbonatite localities have revealed significant isotopic heterogeneity (e.g., Kalt et al., 1997), including some samples that do not fall along the EACL but rather are offset from it, to higher 87Sr/S6Sr or 143Nd/lggNd (Fig. 10). Collectively, the isotopic data demonstrate that large ranges in isotopic composition are present, often over very short distances, within the East African lithospheric mantle.
252
T. Furman, D. Graham/Lithos 48 (1999) 237-262
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87Sr/86Sr Fig. 10. 143Nd//la4Nd vs. 87Sr/86Sr for selected lavas, carbonatites and xenoliths from East Africa. Results for Kivu lavas analyzed in this study are shown by diamonds, separated into Bukavu and Tshibinda groups. Fields for other western rift lavas include Rungwe nephelinites and alkali basalts (Graham et al., in prep.), Toro Ankole lavas and xenoliths (Davies and Lloyd, 1989; Graham et al., in prep.), Karisimbi basanites and potassic basanites (Rogers et al., 1992), Muhavura potassic hawaiites and basanites (Rogers et al., 1998), and undersaturated mafic lavas from small vents and cones in the Virunga province (Vollmer and Norry, 1983). Eastern rift lavas include Naivasha basalts shown by open circles (Davies and Macdonald, 1987) and other lavas from Kenya shown by open triangles (Norry et al., 1980). The field for Huri Hills basanites and alkali basalts is from Class et al. (1994). Stippled fields show carbonatites from the eastern rift; E. Uganda (Tororo, Busuku, Napak and Sukulu; Bell and Blenkinsop, 1987; Nelson et al., 1988); W - - Wasaki peninsula (Kalt et al., 1997), Oldoinyo Lengai (Bell and Simonetti, 1996), K m Kerimasi, N. Tanzania (Kalt et al., 1997). The dashed line is the EACL from Bell and Blenkinsop (1987). Granulite xenoliths from Lashaine, Tanzania are from Cohen et al. (1984), and open diamonds show diopsides from South African kimberlites (Menzies and Murthy, 1980).
Mafic lavas from the eastern and western rift branches define an elongate Sr-Nd isotope array that, to a first approximation, lies parallel to the EACL source (Fig. 10). The isotopic variations in these mafic lavas are clearly decoupled from variations in key trace element ratios that are indicative of crustal contamination, such as C e / P b , and therefore, they must primarily be source region features. Despite the isotopic variability, we can identify consistent regional patterns for lavas from both the eastern and western rift branches. The high eNa values and low 87Sr/86Sr observed at Kivu are similar to some oceanic basalts, suggesting a sub-lithospheric source. The isotopically more enriched (low end) Kivu lavas from Tshibinda volcano trend towards the enriched compositions found in the East African Rift system, such as the primitive-K basanites from Karisimbi (Rogers et al., 1992). The western Virunga vents of Nyiragongo, Goma and Bush-
waga also have isotopic compositions that lie within the Kivu array, whereas mafic lavas from the eastern Virunga volcanoes Karisimbi, Visoke and Muhavura are the most highly enriched lavas for which crustal contamination cannot be demonstrated (Rogers et al., 1992, 1998). More evolved lavas from this area, such as the Sabinyo quartz latites (Vollmer and Norry, 1983), clearly show the effects of crustal contamination, and we have not considered them in the discussion. Isotopic compositions intermediate to these extremes are found at isolated vents in central Virunga (Muganza, Busamba, Mukuyu and Mikeno localities; Vollmer and Norry, 1983). Taken together, lavas from the Kivu and Virunga provinces define a broad Sr-Nd isotope array, termed here the K - V array. The Sr and Nd isotope compositions of a lava along the K - V array correspond roughly to its geographic position: lavas from Tshibinda have isotope compositions overlapping those of western
T. Furman, D. Graham/Lithos 48 (1999) 237-262
Virunga, whereas lavas from the Bukavu group have lower 87Sr/86Sr and those from eastern Virunga have higher 87sr/g6sr (Fig. 10). Sr and Nd isotopic analyses for mafic lavas from Rungwe, and lavas and xenoliths from the ToroAnkole province (Davies and Lloyd, 1989; Graham et al., in preparation) define smaller clusters located between the EACL and the K - V array. Rungwe nephelinites and basanites show a near-horizontal Nd-Sr trend very much like lavas from Toro-Ankole, while Rungwe alkali basalts lie close to the EACL, but are displaced slightly towards the K - V array. While the isotopic data for both the Toro-Ankole and Rungwe suites clearly show that their source regions are heterogeneous, the range of variation is much smaller than that observed in the Kivu and Virunga provinces, and it does not correspond in any simple way to geographic location. Lavas from the eastern branch of the rift have Sr and Nd isotope compositions that overlap both the K - V array and the range of Rungwe and ToroAnkole lavas. Lavas from Huri Hills show lower 87Sr/S6Sr for a given 143Nd/144Nd as compared to the Kivu province, and lie near the most depleted (high end) part of the K - V array (Fig. 10). Among the Naivasha suite, the oldest Pleistocene lavas plot along the K - V array with compositions similar to Nyiragongo and its adjacent vents (Davies and Macdonald, 1987). Later Pleistocene basalts (Naivasha II in Fig. 10) plot among the highest 87Sr/S6Sr samples from Rungwe and Toro Ankole, while Recent Naivasha basalts have isotopic values that fall between the other two age groups. Mafic lavas from northern Tanzania (Paslick et al., 1995) show a range in Sr-Nd isotopes similar to that observed at Naivasha (Fig. 10). Notably, two lavas from Essimingor span the entire range (eNd = 2.4 to --4.9), again indicating a source region that is heterogeneous on a short length scale. 3.5. Isotope and trace element characteristics of lithospheric mantle sources The extreme Sr-Nd isotopic variability of East African Rift lavas requires melting of heterogeneous mantle sources dominantly located in the continental lithospheric mantle (e.g., Vollmer and Norry, 1983; Rogers et al., 1992, 1998; Williams and Gill, 1992).
253
Despite this isotopic variability, western rift lavas show a convergence in S r - - N d - - P b isotopes near values of 87Sr/86Sr ~ 0.7050, 143Nd/144Nd ~ 19.0 (Graham 0.51264 (ey o ~ 0) and 2~176 et al., 1995). The isotopic convergence is defined by a relatively small range of common values found at all western rift and some eastern rift volcanoes. The full range in values for individual provinces extends away from this convergence to distinct compositions characteristic of each area. We observe this convergence among selected lavas from Kivu and Rungwe (data from this study and Graham et al., in preparation), Toro Ankole (Davies and Lloyd, 1989; Graham et al., in preparation), Karisimbi and Muhavura (Rogers et al., 1992, 1998), Naivasha (Davies and Macdonald, 1987) and northern Tanzania (Paslick et al., 1995). Each volcanic province examined, except Huri Hills, has some samples with 87sr/g6sr 0.7050 and 143Nd/144Nd ~ 0.51264 (eNd ~'~ 0 ) (Fig. 10). Mafic lavas from Rungwe and Toro Ankole show a restricted range and lie near the convergence in Sr and Nd isotopes, extending slightly towards the EACL. In contrast, other volcanic areas that display a large isotopic range, including Kivu, Karisimbi, Muhavura, Naivasha and northern Tanzania, define distinct trends in Sr-Nd isotopes that radiate away from the convergence in isotope composition rather than straddling it. This pattern suggests to us that a CLM source having isotope compositions near this convergence is available beneath each of these volcanic areas. The CLM source may, however, be intimately mixed (laterally or vertically) with other source materials having different isotope compositions, and these may be distinct for each volcanic area. Within each volcanic area, many incompatible trace element ratios vary as a function of lava type and/or Sr-Nd isotopic composition (Marcelot et al., 1989; Rogers et al., 1992, 1998; Class et al., 1994; Furman, 1995). Thus, the trace element variations for individual areas typically reflect small-scale intermingling of distinct sources or their derivative melts. Considering the eastern and western rift datasets together, there are certain incompatible trace element ratios, such as L a / N b and Ba/Nb, which overlap among several sample suites, and which also show characteristics consistent with a CLM source identified from Sr-Nd isotopes. Variations in La/Nb,
T. Furman, D. Graham/Lithos 48 (1999) 237-262
254
r ~ Bukavu group
0.5130
Z
r
0.5128
A
Tshibinda group Karisimbi
[] 0 +
Muhvaura Rungwe Tom Ankole
~9
Naivasha II
-
0.5126
0.5124
A 0.5122 0.4
0.6
0.8
1.0 La/Nb
1.2
1.4
0.5130
Z
1.6
B
0.5128
"~ 0.5126
Z
0.5124
0.5122 5
I
I
I
10
15
20
25
Ba/Nb Fig. 11. Relationships between 143Nd/144Nd and incompatible trace element ratios. These variations allow a characterization of the CLM source. Lavas from the Tshibinda group at Kivu, Muhavura, Karisimbi, Rungwe, Toro Ankole and Naivasha define trends that converge at a narrow range of values. See text for full discussion. (A) La/Nb-143Nd/144Nd. (B) Ba/Nb-143Nd/144Nd
143Nd/144Nd
B a / N b and N b / T h against (Fig. 11) reveal a small field of overlapping values among samples from Kivu (Tshibinda), Karisimbi, Muhavura, Rungwe, Toro Ankole and Naivasha. Trends for each volcanic province have different slopes and orientations, but they converge at a common area. Like the S r - N d - P b isotope systematics described by Graham et al. (1995), overlap does not occur at a single value but rather requires a small range and, by inference, some degree of isotopic and trace element heterogeneity in the CLM source.
3.6. Mineralogy of the lithospheric mantle source An accurate knowledge of the source mineralogy for lithospheric melts can place important constraints
on the thermal structure of the subcontinental mantle. In the case of the African Rift system, variations in the depth of melting along and across the rift axes may be used to infer the degree of asthenospheric upwelling and hence, the three-dimensional shape of the plume head. A general picture of the shape of the plume is available from detailed geophysical studies (e.g., Simiyu and Keller, 1997), but the presence of mineralogical barometers such as garnet, amphibole and phlogopite in the source region for mafic rift lavas offers an increase in resolution of the shallow lithospheric structure, and ultimately, it can provide estimates of the rate of lithospheric erosion or thinning. We note that the low estimates of crustal extension across, in particular, the western rift ( < 15%, Ebinger, 1989b), favor a model of lithospheric erosion rather than one of extensional thinning. In this section, we outline the inferred source mineralogy along both rift branches, identifying features of the CLM source as well as those of other parts of the lithospheric mantle that contribute to African rift volcanism. Several lines of evidence suggest that garnet is present in the source regions of most western rift mafic lavas. The high (La/Yb) n values and the concave-upward spidergrams (Fig. 8) of lavas from the Kivu Tshibinda group, Rungwe, Toro Ankole, Karisimbi, Muhavura and Nyiragongo indicate that the HREE are more compatible than LREE and MREE in the source residue. This feature is also present in some, but not all, of the Bukavu group lavas from Kivu. Furman (1995) used a REE inversion model to infer that melting at Rungwe occurs within the spinel-garnet transition zone ( ~ 60-80 km). REE abundances and (La/Yb)n values at Muhavura that are similar to those at Rungwe led Rogers et al. (1998) to infer a comparable melting depth beneath eastern Virunga. In eastern rift lavas, the geochemical evidence for residual garnet in the mantle source is more equivocal, as high ( L a / Y b ) , values are found only in Huri Hills basanites. HREE abundances in lava suites from O1 Tepesi and Naivasha are markedly more variable than those from the western rift volcanoes. Spinel- and garnetbearing lherzolite xenoliths found at Marsabit in northern Kenya and the Chyulu volcanic field in southern Kenya (Henjes-Kunst and Altherr, 1992) suggest that melting occurs at or below the depth
T. Furman, D. Graham/Lithos 48 (1999) 237-262
where garnet becomes stable in these areas. These sites are both located east of the main rift and may record different melting processes than those beneath the rift axis. Relative abundances of the alkali and alkaline earth elements can be used to assess the presence of amphibole and/or phlogopite in the mantle source region. These phases are important because they can attest to the metasomatic enrichment history of the source region, as well as helping to constrain the depth of melting. Both Rb and Ba are compatible in phlogopite (LaTourette et al., 1995), while Rb, Sr and Ba are moderately compatible in amphibole (Adam et al., 1993; LaTourette et al., 1995). Melts in equilibrium with phlogopite are expected to have significantly higher R b / S r and lower B a / R b values than those formed from amphibole-bearing sources. Conversely, melts of an amphibole-bearing source may have extremely high Ba contents and B a / R b values. Several lines of evidence suggest that ultrapotassic lavas from Toro Ankole, Karisimbi and Muhavura formed through melting of a phlogopite-bearing lithospheric mantle source. These lavas have high R b / S r ( > 0.10) and low B a / R b values ( < 20) (Fig. 12). They also incorporate micaceous xenoliths (Holmes and Harwood, 1937; Lloyd and Bailey, 1975; Davies and Lloyd, 1989; Lloyd et al., 1991) and/or phlogopite xenocrysts (Rogers et al., 1998). Experimental stability estimates for phlogopitebearing assemblages suggest melt formation at pressures near 30-35 kbar, or depths of 90-100 km (Olafsson and Eggler, 1983; Wallace and Green, 1988; Lloyd et al., 1991; Sato et al., 1997). In contrast, lavas from many volcanic areas have low KzO/Na20 (< 0.75) and low R b / S r values ( < 0.06, Fig. 12), consistent with melting of an amphibole-bearing source. Tshibinda group lavas from Kivu have higher R b / S r values than Bukavu group lavas with similar B a / R b values, suggesting that a small amount of phlogopite may have been present in the source prior to the onset of melting beneath this area. It is also significant that low-MgO mafic lavas from Muhavura, Karisimbi and Toro Ankole have B a / R b - R b / S r values that overlap those of the Tshibinda group. We suggest that the CLM source is a spinel-garnet lherzolite containing small amounts of amphibole
255
and/or phlogopite and perhaps other minor, metasomatic phases. Dawson and Smith (1988, 1992) describe xenoliths from northern Tanzania that contain both amphibole and phlogopite, and suggest that they result from metasomatic infiltration by ultra-alkaline katungite lava. These observations suggest a widespread enrichment event beneath both the eastern and western rift branches, although a common timing remains to be demonstrated. A small number of alkali basalts from Huri Hills, Naivasha, O1 Tepesi, Rungwe and northern Tanzania have high B a / R b values ( > 50, Fig. 12) that suggest melting of amphibole-bearing (phlogopite-free) lherzolite. In all cases, these samples appear to be contemporaneous with lavas derived from the CLM source. On a local scale, it is difficult to distinguish differences in the history of metasomatic enrichment from differences in phase stability structure of the underlying lithospheric mantle. We therefore suggest that the eruption of lavas closely spaced in time, but derived from mantle regions having very different source mineralogy, is most simply explained by melt generation over a range of depths beneath each volcanic province. The minor phase mineralogy of the CLM source is difficult to constrain and, indeed, may vary on a very short spatial scale (Furman, 1995). In this study, values of N b / T h correlate negatively with R b / S r (Fig. 12) and hence, positively with B a / R b (not shown). This relationship is apparent both within and between suites of lavas, and suggests that the N b / T h systematics of erupted melts may also be controlled by the source mineralogy. We suggest two interpretations that are consistent with the observed regional trends, and that may help further constrain the CLM source mineralogy. First, because Nb is more compatible in amphibole than in phlogopite (LaTourette et al., 1995; Ionov et al., 1997), the progressive removal of phlogopite from amphibole + phlogopite could produce the observed variations. Second, oxide minerals that form during alkali-rich metasomatism may control Nb abundances throughout the melting process (Ionov et al., 1999). Additional work on xenolith suites may prove essential to resolving this question. Class and Goldstein (1997) have discussed evidence for the presence of amphibole and phlogopite in the mantle sources for some ocean island basalts,
256
T. Furman, D. Graham/Lithos 48 (1999) 237-262
A
0.25 9
Tshibinda group
phlogopite
0.20 []
E r,/3
0.15
Bukavu group
;LM~__,
amphibole
O
Rungwe
+
Toro Ankole
[]
Muhavura Karisimbi
0.10 + 0.05
9
)r
IP
@
V
20
0
40
60
80
100
N. Tanzania
@
Naivasha
0
O1 Tepesi Huff Hills
)r
0.00
V
120
Ba/Rb
B
0.20
0.15 []
[]
,.Q 0.10
[] 40
o 4 9
0.05
+
9
+ 9 0.00
<>~>9
9
i
I
I
i
5
10
15
20
25
Nb/Th Fig. 12. Variations in incompatible trace element ratios that may constrain source mineralogy. (A) Rb/Sr vs. Ba/Rb. The mineralogy of the CLM source is inferred to include minor amounts of both amphibole and phlogopite. The field indicated that CLM was drawn to enclose samples identified to have been derived from the CLM source on the basis of isotopic and trace element relationships (see text). High Rb/Sr and Ba/Rb values of all rift samples relative to primitive mantle estimates (PM; Sun and McDonough, 1989) appear to require a widespread enrichment (metasomatic) event. Extremely high Rb/Sr values at Toro Ankole, Muhavura and Karisimbi indicate a greater importance of phlogopite melting in the lithospheric mantle source, whereas high Ba/Rb among eastern rift lavas and Rungwe alkali basalts indicate phlogopite-absent melting of amphibole lherzolite. The amphibole-rich source likely results from carbonatite metasomatism in some cases, whereas abundant phlogopite suggests a relatively higher H 2 0 / C O 2 ratio in the metasomatic agent. (B) Rb/Sr vs. Nb/Th. High Rb/Sr values (indicative of phlogopite in the source region) are correlated with low Nb/Th values. This relationship is consistent with progressive melting of phlogopite from a phlogopite + amphibole lithospheric source, and also with the presence of oxide mineral phases that retain Nb during melting. Both scenarios are consistent with the proposed origin of the CLM source region; see text for discussion.
T. Furman, D. Graham/Lithos 48 (1999) 237-262
and suggest that metasomatism of the oceanic lithosphere by small volume silicate melts plays an important role in ocean island magmatism. In the African western rift, model ages for the different isotope systems suggest metasomatic events beneath Nyiragongo at ~ 490 Ma near the close of the Pan-African (Vollmer and Norry, 1983; Vollmer et al., 1985), and between ~ 750 and 1000 Ma during the Kibaran orogeny (Rogers et al., 1992; Graham et al., in preparation) for the CLM source. The correspondence of model ages with known orogenic events is consistent with a lithospheric mantle source for the trace and minor element inventory of most western rift volcanics (Rogers et al., 1992). Relics of much older events, perhaps dating to Archean, may also be preserved in their Pb isotope compositions (Rogers et al., 1992; Graham et al., in preparation), but modeling of those multi-stage histories is more uncertain. The pattern of R E E / H F S E enrichment observed at Rungwe, Nyiragongo, Toro Ankole and the Tshibinda sector of Kivu (Fig. 7) is indicative of carbonatite metasomatism, but the effects appear to be geographically restricted and may be unrelated to formation of the amphibole- and phlogopite-bearing CLM source. It is worth noting that lavas from two of the areas affected by carbonatite metasomatism, Rungwe and Toro Ankole, have Sr-Nd isotope compositions that trend from the CLM source towards the EACL.
3.7. Inferred variations in lithosphere thickness and erosion Our observations suggest that the CLM source is available beneath the entire African Rift system, an area of roughly 1,000,000 km 2. The evidence for amphibole, phlogopite, spinel and garnet in this mantle source suggests that the most prevalent depth of lithospheric melting is roughly 65-80 km. Ultrapotassic lavas from eastern Virunga and Toro Ankole require melting at depths greater than ~ 80 km, whereas alkali basalts from Rungwe, Huri Hills and Naivasha indicate melting at depths shallower than ~ 65 km. In addition, other lithospheric mantle sources identified by the range of isotopes and trace elements for individual volcanic areas suggest
257
variations in lithospheric thickness over short distances. At Huri Hills, and in the Tshibinda and Bukavu sectors of the Kivu province, lavas show trends towards isotope compositions resembling those for some ocean island basalts (HIMU-like, in the terminology of Zindler and Hart, 1986). This observation suggests that there may be a significant sub-lithospheric contribution in these two areas, and that the lithospheric mantle may contribute little, if any, melt to local magmatism. This Kivu mantle source clearly has all the trace element and isotopic (Sr, Nd, Pb and He) characteristics found at HIMU oceanic islands such as St. Helena (Weaver, 1991; Graham et al., 1992, 1995). Based on geochemical arguments alone, the origin of the Kivu lavas is equivocal. They may represent magmas derived by melting of metasomatized subcontinental lithosphere (e.g., McKenzie and O'Nions, 1995). Alternatively, they may have a deeper, mantle plume origin. The presence of a plume in the region is consistent with the geophysical arguments for the uplift of the East African Plateau (e.g., Griffiths and Campbell, 1991). The wide range in isotope and trace element compositions in the Kivu volcanic province, from HIMU type to CLM source values, appears consistent with strong interaction of upwelling plume material with the lithosphere beneath this area. This implies active lithospheric erosion, but confined to a relatively small area in the western rift. Our inferred lithospheric thickness variations based on geochemical arguments are generally consistent with evidence from gravity surveys and seismic profiles carried out throughout the rift system (e.g., KRISP Working Group, 1987, 1991; Simiyu and Keller, 1997). In the eastern rift, the lithosphere is thinnest beneath the Huri Hills region: seismic profiles and gravity models indicate a crustal thickness of ~ 20 km and in some areas do not require the presence of any lithospheric mantle (e.g., Hendrie et al., 1994; Simiyu and Keller, 1997). The mantle velocity structure inferred from seismic refraction and wide-angle reflection experiments (e.g., KRISP Working Group, 1987, 1991) suggest that the onset of melting occurs at a depth of ~ 65 km. This conclusion is compatible with the range of erupted mafic lavas, which include both plume-like (HIMU) compositions and lithospheric melts, as well as the
258
T. Furman, D. Graham/Lithos 48 (1999) 237-262
inferred presence of garnet in the mantle source (Class et al., 1994). Both crust and lithosphere thicken away from Huri Hills: garnet- and spinel-lherzolite xenoliths suggest crustal and lithospheric thicknesses of 30 and 45 km, respectively, east of the rift at Marsabit (Henjes-Kunst and Altherr, 1992). Xenolith equilibration temperatures and pressures suggest that the crust thickens to a maximum depth of 42 km and a lithosphere which is ~ 73 km thick in southern Kenya; the lithospheric thickness increases to ~ 100 km in northern Tanzania (Henjes-Kunst and Altherr, 1992; Dawson, 1994). Lavas from Naivasha that sample the CLM source therefore occur in an area with crustal thickness between 30 and 42 km, and lithospheric thickness between 45 and 73 km, i.e., at depths of 75-115 km. In the western rift, our interpretations generally agree with those based on geophysical investigations, although they differ slightly in detail. Geochemical considerations would indicate that the lithosphere is thickest beneath Toro Ankole and the eastern Virunga province. Away from there, the lithosphere thins rapidly westward towards Kivu and gradually southward towards Rungwe. Simiyu and Keller (1997) infer a mantle gravity anomaly at a depth of ~ 60 km beneath the western rift axis, centered between the Virunga and Toro Ankole provinces. In their model, the depth to the mantle anomaly decreases to 50 km at 3~ latitude (south of the Kivu province), and increases rapidly to the north, where the anomaly cannot be recognized at 3~ latitude. This implies that any actively upwelling asthenosphere is most likely to be present beneath the northern portions of Lake Tanganyika and beneath the southern (Bukavu) sector of the Kivu province. We suggest that elsewhere along the western rift, the asthenosphere has not been able to ascend to sufficiently shallow depths for melting, because tectonic extension and lithospheric erosion are both very limited. This is supported by the observation that many of the lavas erupted in Quaternary time carry a record of melting of a phlogopite-bearing clinopyroxenite source. Our preferred explanation, based on the geochemical and geophysical observations, is that lithospheric erosion (i.e., to depths shallower than ~ 60-80 km) appears to be restricted in the western rift to the southern portions of the Kivu volcanic province and the northern portions of Lake Tanganyika.
4. Summary Mafic lavas from the Kivu volcanic province display a wide range in incompatible trace element abundances (e.g., crossing REE patterns) and Sr-Nd isotope ratios. All Kivu lavas have elevated incompatible trace element contents relative to MORB and the estimated primitive mantle, requiring that the source region has been enriched by one or more metasomatic events. Samples from Tshibinda volcano, which lies on a major rift border fault at the northwestern margin of the province, have geochemical features that are distinct from the majority of Kivu (Bukavu) lavas. Tshibinda lavas have, for example, the highest values of 87Sr/S6Sr, ( L a / S m ) n, Ba/Nb, and Z r / H f observed among Kivu samples. Sr-Nd isotopic values at Tshibinda trend towards enriched compositions found in the neighboring Virunga province, while Bukavu group lavas include the lowest 87Sr/S6Sr and highest end measured in western rift lavas. The Tshibinda lavas are geochemically distinct within the Kivu province, but their Sr-Nd isotopic compositions and certain incompatible trace element ratios (e.g., La/Nb, Ba/Nb, Rb/Sr) trend towards values that are common to several rift volcanic provinces. Graham et al. (1995) demonstrated that selected lavas from the Kivu, Virunga, Toro Ankole and Rungwe volcanic provinces have S r - N d - P b isotopic compositions that converge upon a narrow range of values, and inferred the existence of a CLM source region. There are consistent trace element characteristics of the CLM source as well, and they help to constrain its mineralogy. This source material appears to be present beneath both the eastern and western rift branches. The CLM source contains small amounts of both amphibole and phlogopite, as indicated by the geochemistry of mafic lavas and supported by the mineralogy of mantle xenoliths found in northern Tanzania (Dawson and Smith, 1988, 1992). This modal mineralogy requires at least one metasomatic enrichment event, which Dawson and Smith (1988) attribute to ultra-alkaline katungite. Models of REE abundances in mafic rift lavas (Latin et al., 1993; Furman, 1995) and lherzolite xenoliths from Kenya suggest that melting dominantly occurs near the spinel-garnet transition ( ~ 60-80 km), where both
259
T. Furman, D. Graham / Lithos 48 (1999) 237-262
phlogopite and amphibole are likely to be stable in the continental lithosphere. Based on experimental studies (e.g., Lloyd et al., 1991), some ultrapotassic lavas from Toro Ankole and the Virunga province are derived by melting of a more phlogopite-rich source, and therefore probably originate from somewhat greater depths than the CLM source (cf. Olafsson and Eggler, 1983). The geochemical evidence allows estimates of variations in lithospheric thickness along the eastern and western rift branches, and these variations are generally consistent with those inferred from geophysical evidence. In the eastern rift, it is significant that the CLM signature is not observed in mafic lavas from Huri Hills, Kenya, where geophysical studies (e.g., Hendrie et al., 1994; Simiyu and Keller, 1997) do not require any lithospheric mantle to be present between the crust and upwelling asthenosphere. Both the crust and lithosphere thicken southward, and in the Naivasha region, their combined thickness may be as much as 75-115 km (HenjesKunst and Altherr, 1992; Simiyu and Keller, 1997). In the western rift, the lithosphere is thickest beneath eastern Virunga and Toro Ankole, and thinnest near
the Bukavu sector of the Kivu province. These observations suggest that the Kivu province is above a region of active lithospheric erosion, where interaction between upwelling asthenosphere and metasomatized lithosphere produces the very wide range in isotopic and trace elemental signatures of the erupted lavas.
Acknowledgements Funding for this research comes from the Earth Sciences Division of NSF (grants 9508112 to T.F., 9304156 and 9614508 to D.G.). We are grateful to C. Ebinger for providing samples, to M. Rhodes and M. Chapman for patient assistance in obtaining XRF analyses, and to F. Frey and P. Ila for their generosity in providing INAA. D.G. thanks George Tilton for graciously providing access to the clean lab and mass spectrometer at UCSB. T.F. thanks A. Upchurch for her careful work in helping prepare the maps. Thoughtful comments from W. McDonough, N. Rogers and an anonymous reviewer helped improve the final manuscript.
Appendix A. Petrographic descriptions of Kivu thin sections Sample
Petrographic description
Percentage of phenocrysts
R3L
Porphyritic, with 1-2 mm phenocrysts of cpx (zoned) and oliv (3:1) in ground mass of opaque oxides + plag + cpx Porphyritic, with 1-3 mm phenocrysts of plag (zoned, twinned, occasionally corroded), oliv (typically corroded), cpx (zoned, twinned, typically corroded, with reaction coronae) (6:3:2) in a groundmass of plag + oliv + opaque oxides Porphyritic, with 1-2 mm phenocrysts of oliv (euhedral), with less abundant plag + cpx (5:2:3) in a groundmass of plag (oriented flow) + cpx + oliv + opaque oxides Microcrystalline, with sparse phenocrysts (0.5 mm) of cpx + oliv with rare plag (2:2:1), in a groundmass of plag + opaque oxides Microcrystalline, with sparse phenocrysts (1-2 ram) primarily oliv > plag (4:1); oliv replaced locally by serpetine; groundmass of plag + oliv + cpx + opaque oxides Porphyritic, with 0-1.5 mm euhedral phenocrysts of oliv (some rimmed by cpx) + cpx (3:7), replaced locally by serpetine; groundmass of opaque oxides + plag + cpx
25
R3K
R4HA
R2J B10C
R4Q
40
40
20 15
35
260
R5A1
R5N
R6C Z7Z
Z3D
Z5G Z6A Z6B
T. Furman, D. Graham/Lithos 48 (1999) 237-262
Moderately porphyritic, with phenocrysts (0.5-1.5 mm) of euhedral oliv + cpx (2:3), oliv replaced locally by serpetine and corroded; in a groundmass of plag + cpx + opaque oxides Phenocrysts ( < 1 mm, euhedral) of oliv + cpx + plag (2:2:1) in a groundmass of plag + oliv + cpx + opaque oxides Moderately porphyritic, with phenocrysts of oliv (2 mm) + cpx(1 mm) + plag (0.5 mm) (2:7:1) in groundmass of plag + cpx + opaque oxides Phenocrysts of plag ( ~ 1 mm) + oliv (1-1.5 mm) and minor cpx (1 mm) (2:2:1) in medium-grained groundmass ( ~ 0.5 mm) of plag + cpx + opaque oxides Phenocrysts of plag ( ~ 1 mm) + oliv (1-1.5 mm) and minor cpx (1 mm) (2:2:1) in medium-grained groundmass ( ~ 0.5 mm) of plag + cpx + opaque oxides Sparsely phyric, with 1-2 mm phenocrysts of cpx > oliv > plag (4:3:2) in groundmass of opaque oxides + plag + cpx Porphyritic, with 2-3 mm euhedral phenocrysts of cpx < oliv (2:3), in a groundmass of plag + cpx + opaque oxides Porphyritic, with 2-3 mm euhedral phenocrysts of cpx > oliv (3:2), in a groundmass of plag + cpx + opaque oxides
References Adam, J.D., Green, T.H., Sie, S.H., 1993. Proton microprobe determined partitioning of Rb, Sr, Ba, Y, Zr, Nb and Ta between experimentally produced amphiboles and silicate melts with variable F content. Chem. Geol. 109, 29-49. Auchapt, A., Dupuy, C., Dostal, J., Kanika, M., 1987. Geochemistry and petrogenesis of rift-related volcanic rocks from South Kivu (Zaire). J. Volcanol. Geotherm. Res. 31, 33-46. Baker, B.H., Williams, L.A.J., Miller, J.A., Fitch, F.J., 1971. Sequence and geochronology of the Kenya Rift volcanics. Tectonophysics 11, 191-215. Baker, B.H., Goles, G.G., Leeman, W.P., Linstrom, M.M., 1977. Geochemistry and petrogenesis of a basalt-benmoreitetrachyte suite from the southern part of the Gregory Rift, Kenya. Contrib. Mineral. Petrol. 64, 303-332. Bell, K., Blenkinsop, J., 1987. Nd and Sr isotopic compositions of East African carbonatites: implications for mantle heterogeneity. Geology 15, 99-102. Bell, K., Doyle, R.J., 1971. K-Rb relationships in some continental alkaline rocks associated with the East African Rift valley system. Geochim. Cosmochim. Acta 35, 903-915. Bell, K., Powell, J.L., 1969. Strontium isotopic studies of alkalic rocks: the potassium-rich lavas of Birunga and Toro-Ankole regions, east and central equatorial Africa. J. Petrol. 10, 536-572. Bell, K., Simonetti, A., 1996. Carbonatite magmatism and plume activity: implications from the Nd, Pb and Sr isotope systematics of Oldoinyo Lengai. J. Petrol. 37, 1321-1339.
40
25 30 30
20
45 25 30
Bellon, H., Pouclet, A., 1980. Datations K-Ar de quelques laves du Rift-ouest de l'Afrique Centrale: implications sur l'~volution magmatique et structurale. Geologische Rundschau 69, 49-62. Boynton, W.V., 1983. Cosmochemistry of the rare earth elements: meteorite studies. In: Henderson, P. (Ed.), Rare Earth Element Geochemistry. Elsevier, New York, pp. 63-114. Class, C., Goldstein, S.L., 1997. Plume-lithosphere interactions in the ocean basins: constraints from the source mineralogy. Earth Planet. Sci. Lett. 150, 245-260. Class, C., Altherr, R., Volker, F., Eberz, G., McCulloch, M.T., 1994. Geochemistry of Pliocene to Quaternary alkali basalts from the Huri Hills, northern Kenya. Chem. Geol. 113, 1-22. Cohen, R.S., O'Nions, R.K., Dawson, J.B., 1984. Isotope geochemistry of xenoliths from East Africa: implications for development of mantle reservoirs and their interaction. Earth Planet. Sci. Lett. 68, 209-220. Davies, G.R., Lloyd, F.E., 1989. Pb-Sr-Nd isotope and trace element data bearing on the origin of the potassic subcontinental lithosphere beneath south-west Uganda, Kimberlites and Related Rocks. Geol. Soc. Aust. Spec. Publ., Vol. 14. Blackwell, Perth, pp. 784-794. Davies, G.R., Macdonald, R., 1987. Crustal influences in the petrogenesis of the Naivasha basalt-comendite complex: combined trace element and Sr-Nd-Pb isotope constraints. J. Petrol. 28, 1009-1031. Dawson, J.B., 1994. Quaternary kimberlitic volcanism on the Tanzanian craton. Contrib. Mineral. Petrol. 116, 473-485. Dawson, J.B., Smith, J.V., 1988. Metasomatised and veined up-
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Marcelot, G., Dupuy, C., Dostal, J., Rancon, J.P., Pouclet, A., 1989. Geochemistry of mafic volcanic rocks from the Lake Kivu (Zaire and Rwanda) section of the western branch of the African Rift. J. Volcanol. Geotherm. Res. 39, 73-88. McDonough, W.F., 1990. Constraints on the composition of the continental lithospheric mantle. Earth Planet. Sci. Lett. 101, 1-18. McKenzie, D., O'Nions, R.K., 1995. The source regions of ocean island basalts. J. Petrol. 36, 133-159. Menzies, M.A., Murthy, V.R., 1980. Enriched mantle: Nd and Sr isotopes in diopsides from kimberlite nodules. Nature 283, 634-636. Mitchell, R.H., Bell, K., 1976. Rare earth element geochemistry of potassic lavas from the Birunga and Toro-Ankole regions of Uganda, Africa. Contrib. Mineral. Petrol. 58, 293. Nelson, D.R., Chivas, A.R., Chappell, B.W., McCulloch, M.T., 1988. Geochemical and isotopic systematics in carbonatites and implications for the evolution of ocean-island sources. Geochim. Cosmochim. Acta 52, 1-17. Norry, M.J., Truckle, P.H., Lippard, S.J., Hawkesworth, C.J., Weaver, S.D., Marriner, G.F., 1980. Isotopic and trace element evidence from lavas, bearing on mantle heterogeneity beneath Kenya. Philos. Trans. R. Soc. London, Ser. A 297, 259-271. Olafsson, M., Eggler, D.H., 1983. Phase relations of amphibole, amphibole-carbonate and phlogopite-carbonate peridotite: petrologic constraints on the asthenosphere. Earth Planet. Sci. Lett. 64, 305-315. Paslick, C., Halliday, A., James, D., Dawson, J.B., 1995. Enrichment of the continental lithosphere by OIB melts: isotopic evidence from the volcanic province of northern Tanzania. Earth Planet. Sci. Lett. 130, 109-126. Pasteels, P., Villeneuve, M., De Paepe, P., Klerkx, J., 1989. Timing of the volcanism of the southern Kivu province: implications for the evolution of the western branch of the East African Rift system. Earth Planet. Sci. Lett. 94, 353-363. Rogers, N.W., De Mulder, M., Hawkesworth, C.J., 1992. An enriched mantle source for potassic basanites: evidence from Karisimbi volcano, Virunga volcanic province, Rwanda. Contrib. Mineral. Petrol. 111,543-556. Rogers, N.W., James, D., Kelley, S.P., DeMulder, M., 1998. The generation of potassic lavas from the eastern Virunga province, Rwanda. J. Petrol. (in press).
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LITHOS
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Lithos 48 (1999) 263-285
Trace element compositions of minerals in garnet and spinel peridotite xenoliths from the Vitim volcanic field, Transbaikalia, eastern Siberia Sandra M. Glaser a, Stephen F. Foley a,*, Detlef Giinther b a
Mineralogisch-Petrologisches Institut, Uniuersitiit Gi#tingen, GoldschmidtstraJ3e 1, D-37077 G6ttingen, Germany b Laboratory of Inorganic Chemistry, ETH Ziirich, Uniuersitiitsstrasse 6, CH-8092 Ziirich, Switzerland
Received 23 April 1998" received in revised form 15 January 1999" accepted 18 January 1999
Abstract Peridotite xenoliths from the Bereya alkali picrite tuff in the Vitim volcanic province of Transbaikalia consist of garnet lherzolite, garnet-spinel lherzolite and spinel lherzolite varieties. The volcanism is related to the Cenozoic Baikal Rift. All peridotites come from pressures of 20-23 kbar close to the garnet to spinel peridotite transition depth, and the presence of garnet can be attributed to cooling of spinel peridotites, probably during formation of the lithosphere. The peridotites show petrographic and mineral chemical evidence for infiltration by an alkaline silicate melt shortly before their transport to the Earth's surface. The melt infiltration event is indicated petrographically by clinopyroxenes which mimic melt morphologies, and post-dates outer kelyphitic rims on garnets which are attributed to an isochemical heating event within the mantle before transport to the Earth's surface. Single-mineral thermometry gives reasonable temperature estimates of 1050_ 50~ whereas two-mineral methods involving clinopyroxene are falsified by secondary components in clinopyroxene introduced during the melt infiltration event. Excimer Laser-ICP-MS analysis has been performed for an extensive palette of both incompatible and compatible trace elements, and manifests the most thorough dataset available for this rock type. Orthopyroxene and garnet show only partial equilibration of trace elements with the infiltrating melt, whereas clinopyroxene and amphibole are close to equilibration with the melt and with each other. The incompatible element composition of the infiltrating melt calculated from the clinopyroxene and amphibole analyses via experimental mineral/melt partition coefficients is similar to the host alkali picrite, and probably represents a low melt fraction from a similar source during rift propagation. The chemistry and chronology of the events recorded in the xenoliths delineates the series of events expected during the influence of an expanding rift region in the upper mantle, namely the progressive erosion of the lithosphere and the episodic upward and outward propagation of melts, resulting in the evolution of the Vitim volcanic field. 9 1999 Elsevier Science B.V. All rights reserved. Keywords: Peridotite" Xenolith; Melt infiltration; Trace element; Garnet; Spinel; Vitim
1. Introduction Garnet peridotites form the dominant rock type in cratonic mantle xenolith suites brought to the Earth's
* Corresponding author
surface by kimberlites (Dawson, 1980; Harte, 1983), but are very rare in non-cratonic xenolith suites hosted by alkali basaltic volcanics. This presumably indicates that the generation of alkali basalts and basanites, which are the host lavas to most noncratonic spinel lherzolite xenolith suites (Menzies,
0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All rights reserved. PII: S0024-4937(99)00032-8
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S.M. Glaser et a l . / Lithos 48 (1999) 263-285
1983) is too shallow to sample garnet peridotites, and that exceptional tectonic circumstances are required to permit sampling in the garnet stability field. Examples of non-cratonic garnet peridotites which have been described to date appear to occur either in a behind-arc setting entrained in volcanics triggered by asthenospheric upwelling in response to subduction, such as those at Mingxi and Xilong in southeastern China (Cao and Zhu, 1987) and at Pali Aike in southern South America (Skewes and Stern, 1989; Stern et al., 1989), or they occur in rift-related volcanic settings on the flanks of continental rifts, such as the Vitim Plateau in Transbaikalia, eastern Siberia (Ionov et al., 1993) and at the Jetty Peninsula on the flanks of the Lambert-Amery rift in eastern Antarctica (Andronikov, 1990; Andronikov et al., 1998). Cratonic peridotite xenoliths sampled by kimberlites generally represent very old lithospheric mantle (Pearson, 1998), whereas xenoliths in non-cratonic volcanic provinces represent younger lithospheric mantle domains (Menzies, 1990). Consequently, studies of non-cratonic garnet facies xenoliths hosted in basaltic rocks furnish direct information about the composition of lower levels of the lithospheric mantle away from the cratons and allow us to compare the two xenolith suites and recognise any differences in the development of the lithospheric upper mantle through time. In this report we present petrographic and mineral chemical details (in situ major and trace element analyses) of newly collected peridotite xenoliths from the Vitim plateau, Eastern Siberia. These peridotites experienced infiltration by melts similar to the host alkali picrites shortly before they were brought to the Earth's surface, and thus represent a case of rift-related metasomatism of garnet peridotites.
summarized by Kiselev (1987). Spinel lherzolite xenoliths have been described from several localities such as Bartoy (Ionov et al., 1992) and the Shavaryn-Tsaram volcano in the Tariat field (Press et al., 1986; Stosch et al., 1986) (Fig. 1), but garnetbeating peridotites are known only from the Vitim plateau. Seismic, electrical conductivity and density data indicate that the Baikal rift zone is underlain by anomalous mantle; the seismic velocity at the Moho discontinuity is 0.5 k m / s less than under the Siberian platform (Zorin, 1981). It is debated whether the rifting in this region is due to active upwelling of the asthenosphere (Zorin, 1981; Logatchev and Zorin, 1992) or is passive (Kiselev and Popov, 1992). The Baikal Rift was initiated by a change in the intra-plate stress regime of this area as a result of the collision of India and Eurasia in Eocene times, and has developed over the last 30 Ma. The lithosphere beneath the Vitim volcanic field is about 100-125 km thick, and thins rapidly to the northwest, forming the southeasterly flank of the expression of the Baikal Rift in the upper mantle (Fig. 1). Volcanism in the Vitim plateau area started with the eruption of alkali olivine basalts in the Miocene and continued through the eruption of Quaternary basanites and hawaiites. The samples studied here are from a single occurrence of Miocene alkali picritic tufts at the Bereya quarry, which is the locality referred to by Ionov et al. (1993) as the "tuff pit". The Bereya quarry is located towards the eastern edge of the Vitim province, and a K / A r age of 16.3 Ma is reported by Esin et al. (1995) for the host alkali picrite tuff. Due to the abundance of garnet peridotites the Bereya quarry is unique even within the Vitim area: garnet or garnet-spinel bearing varieties make up about 80% of the lherzolite xenoliths.
3. Petrography and mineral chemistry 2. Geological setting The Vitim volcanic province is located about 200 km east of Lake Baikal (Fig. 1) close to the Vitim and Dzhilinda rivers. The magmatic activity in this area is associated with the thinning of the lithosphere and the rifting process in the Baikal rift zone, and is
Most of the xenoliths were collected from the Romanovka-Bagdarino road and others directly from the Bereya quarry from which the road material was excavated. Ionov et al. (1993) remarked that the Vitim peridotites show little evidence for metasomatic enrichment, although they focused their atten-
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S.M. Glaser et al. / Lithos 48 (1999) 2 6 3 - 2 8 5
108 ~
56 ~ 102 ~
114 ~-
ian /Platform 150 100
Irkutsk
Chita o /
J Hubsug
~/ /
/
~125
/
Fig. 1. Geological setting of the Vitim volcanic province showing positions of volcanic fields (black areas) associated with the Baikal Rift and contours of depths to the base of the lithosphere as defined by Zorin et al. (1989). Large towns are shown in italics. The Bereya alkali-picrite garnet peridotite xenolith locality lies at the eastern edge of the Vitim volcanic field ("tuff pit" locality in Ionov et al., 1993).
tion on rare large samples (up to 30 cm) in a study aimed at comparing the least metasomatised garnet peridotites from cratonic and non-cratonic regions. We have investigated the more common smaller samples, which have an average size of 5-6 cm, and can be subdivided into several groups: (1) garnet lherzolites, (2) garnet-spinel lherzolites, (3) spinel lherzolites, and (4) pyroxenites. Amphibole- and phlogopite-bearing examples of all groups except the garnet peridotites are represented in our collection. We have concentrated on the lherzolite xenoliths; information on the variable and extensive pyroxenite suite and on other xenolith types such as megacrysts and granulites is given elsewhere (Ashchepkov et al., 1994; Andr6 and Ashchepkov, 1996; Litasov and Litasov, 1999). Seven xenoliths were selected as representatives of the peridotite groups for in situ trace element analysis by Laser-ICP-MS. The following description of petrographic and mineral
chemical features is based on these selected samples but is representative of the suite as a whole.
3.1. Petrographic features of the Bereya peridotites The xenoliths of the peridotite groups consist of variable amounts of olivine, orthopyroxene and clinopyroxene (4-21 vol.% with the exception of one harzburgite sample, determined by point counting; Fig. 2, Table 1). This confirms the observation of Ionov et al. (1993) that the peridotites vary between depleted and fertile compositions, whereby fertile compositions are much commoner than in most mantle regions, including garnet lherzolites from cratonic regions (Boyd, 1989; Boyd et al., 1997; Rudnick et al., 1994) and spinel lherzolites from non-cratonic regions (Frey and Prinz, 1978; Bernstein et al., 1998). Minor phases include garnet
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O1
Table 1 Mineral modes in Bereya peridotites Modes are given in vol.% as determined by point counting in thin section. Trace element analyses are available for samples marked with an asterisk.
~fDunite 8 9
(
Harzburgit
)
~
A
50 40
i
Opx
i
Cpx
Fig. 2. Modal mineralogy of xenoliths from Bereya compared to Kaapvaal garnet lherzolites (open circles; Nixon, 1987) and depleted spinel lherzolites from Wiedemann, West Greenland (shaded field; Bernstein et al., 1998) showing the higher abundance of clinopyroxene in the Bereya samples (filled symbols: circles = garnet peridotites, squares = garnet spinel peridotites, triangles = spinel peridotites).
( 2 - 1 2 v o l . % ) a n d / o r spinel ( 0 . 3 - 1 . 3 vol.%), and m a n y rocks contain rare p h l o g o p i t e a n d / o r amphibole (generally less than 1 vol.%). H o w e v e r , our suite does not contain the a m p h i b o l e - p h l o g o p i t e veins d e s c r i b e d by I o n o v et al. (1993), p r e s u m a b l y due to the smaller size of the samples. W e retain the n o m e n c l a t u r e of I o n o v et al. (1993) in r e s e r v i n g the t e r m garnet peridotite for rocks w h i c h contain only spinel as inclusions in garnet, w h e r e a s g a r n e t - s p i n e l peridotites also contain larger
Sample
O1
Opx
Cpx
SF-93102 SF-93193 SF-93200 SF-93207 SG-96B14 SF-93112 SF-93118 SG-96Bll* SF-93163" SF-93205" SF-93182 SG-96B13*
56.6 53.2 63.6 55.7 52.2 75.2 63.1 68.7 63.5 71.1 55.2 57.1
24.7 30.3 22.0 22.5 24.6 19.7 14.7 28.2 15.4 12.4 17.3 26.7
16.0 2.1 13.1 1.7 9.6 2.0 10.0 11.8 20.6 2.6 4.1 19.7 0.5 13.3 6.6 11.2 5.4 16.9 8.9 13.6 1.9
Gt
Sp 0.7 0.7 0.8 < 0.35 0.7 0.9 1.1 1.3 <0.4 < 0.4 0.3
Amph
Phl
0.8
0.5
1.3 0.5
spinel grains outside garnet. I o n o v et al. (1993) s h o w e d by reference to a c o m p o s i t e xenolith that this distinction m a y be due largely to differences in bulk c o m p o s i t i o n and not to depth of origin. Textural relations are c o m p a t i b l e with the f o r m a t i o n of garnet by the reaction spinel + c l i n o p y r o x e n e + o r t h o p y r o x e n e garnet + olivine w h i c h is often d o c u m e n t e d by inclusions of the reactant minerals within garnet, and the restriction of spinel to inclusions within garnet in the garnet peridotites. Early and late stages of the reaction h a v e also b e e n found in B e r e y a samples.
Fig. 3. Photomicrographs of the Bereya lherzolite xenoliths. (a) Typical texture of lherzolites showing elongate grains with equilibrium 120~ triple junctions. Photo width = 4.5 mm. (b) Sheared spinel lherzolite with porphyroclasts of olivine, orthopyroxene and clinopyroxene in mosaic matrix of the same minerals which lacks the strong preferred orientation typical of sheared xenoliths in kimberlites. Photo width = 4.5 mm. (c) Phlogopite-bearing lherzolite contrasting the textures of the two clinopyroxene generations. The first (Cpx-1) forms approximately equant grains 0.2-2 mm across and is interpreted as an integral part of the lherzolite prior to melt infiltration. Grain boundaries are often concave against olivine and orthopyroxene. The second generation (Cpx-2) forms optically continuous crystals filling interstitial passageways between several crystals of the original lherzolite. A late recrystallised rim (10-100 lxm wide) occurs on both generations. Photo width - 4.5 mm. (d) Infiltration and breakdown textures in garnet lherzolite. Garnet (Gt) grains and subgrains are reacted to form a thin brown kelphitic rim (Kp). Second generation Cpx (Cpx-2) forms interstitial networks around other minerals and has thin recrystallised rims (cr) interpreted as being formed by decompression breakdown during ascent to the Earth's surface. Photo width = 4.5 mm. (e) Clinopyroxene interstitially occupying a triple junction between olivine and opx forming apparent dihedral angles much too small for textural equilibrium between these minerals. Circular structures are ablation pits from LAM-ICP-MS analysis of 40-80 Ixm diameter. Photo width = 0.55 mm. (f) Larger area including the area of (e) (upper left) showing that cpx surrounds earlier minerals and replaces melt morphology. Photo width = 1.1 mm.
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The textures of the peridotites are similar to the typical protogranular type of spinel peridotites from alkali basalts (Mercier and Nicolas, 1975), with garnet forming irregular grain shapes. Crystals generally have straight or gently curved boundaries and show only little evidence of strain in the form of undulose
267
extinction. Typical grain sizes for olivine and orthopyroxene are 2-4 ram, for spinel approximately 0.2 ram, whereas garnet ranges in size from 0.5 up to 6.5 ram. Olivine often forms elongated prismatic grains resulting in a weak preferred orientation, although even here triple-grain junctions approach 120 ~
268
S.M. Glaser et al. ,/Lithos 48 (1999) 263-285
angles (Fig. 3a). An exception is sample SF-93162 which shows a strongly deformed porphyroclastic mosaic texture consisting of a fine-grained matrix of recrystallized olivine, orthopyroxene and clinopyroxene surrounding porphyroclasts of the same phases (Fig. 3b). This xenolith contains veins of glass probably resulting from contact with the ascending magma. Amphibole appears only in spinel-harzburgite sample SG-96B 11 and in the pyroxenite SF-93803. In sample SF-93803 amphibole forms a vein through the xenolith and is surrounded by a thin mosaic rim of orthopyroxene and olivine, whereas in sample SG-96B 11 it appears as well-rounded inclusions (up to 200 txm) in all lherzolite mineral phases. Phlogopite-bearing examples of both garnet-spinel (SG96B13) and spinel lherzolites (SG-96B 11) have been studied. Phlogopite occurs as large (2-3 mm) subequant to elongate strongly pleochroic crystals (Fig. 3c) often with glass on grain boundaries, particularly in contact with orthopyroxene. Clinopyroxene occurs as two texturally distinguishable generations. The first consists of approximately equant grains 0.2-2 mm across (Cpx-1 in Fig. 3c), many of which appear xenomorphic due to grain boundaries which are concave towards the clinopyroxene (Fig. 3c, centre). The second generation consists mostly of long irregular crystals which form optically continuous interstitial networks between several other mineral grains; these may be continuous over 2 cm in section or surround several surfaces of olivine or garnet crystals (Cpx-2 in Fig. 3c,d,f). Clinopyroxenes of both generations usually have thin reacted rims consisting of recrystallised clinopyroxene and glass (Fig. 3c and d); these occur irrespective of the identity of the neighbouring grain, and were probably produced within the host magma during transport to the Earth's surface. Garnets exhibit two types of reaction corona, a ubiquitous, microscopically amorphous brown rim (Kp-1; Fig. 3d) reminiscent of kelyphites in garnet lherzolites and garnet megacrysts in kimberlites, and a very fine-grained intergrowth of clinopyroxene, orthopyroxene and greenish spinel (Kp-2) forming a reaction zone generally not more than 50 txm wide. The first type is present also on subgrain boundaries, whereas the second occurs discontinuously on outer rims of garnets in contact with other silicate phases.
The reaction forming Kp-2 is the reverse of the garnet-building reaction and may be isochemical, in contrast to the kelyphite-forming reaction in many peridotites entrained in kimberlites, which appear to require the introduction of a metasomatic component (Hunter and Taylor, 1982). Kp-2 occurs outside Kp-1 and rarely between Kp-1 and the recrystallised rims of clinopyroxenes (cr in Fig. 3d). Some textural features of the second generation clinopyroxenes may be explained by the infiltration of melt into the peridotites within the mantle. The irregular shapes of Cpx-2 with extreme aspect ratios (Fig. 3c,d,f) and very low contact angles ( < 40 ~ between Cpx-2 and olivine and/or orthopyroxene (Fig. 3e) indicate the crystallisation of Cpx-2 in space previously occupied by a melt: the morphology of Cpx-2 and the low apparent dihedral angles resemble those of melt pockets in partially molten ultramafic rocks (Faul, 1997; Cm~ral et al., 1998). Dihedral angles such as in Fig. 3e are far too small to represent equilibrium contact angles between silicate minerals; measurements on a similar occurrence in the Inagli dunite of eastern Siberia show some of these contact angles to be close to those expected for olivine/melt and orthopyroxene/melt (Zinngrebe et al., 1995), whereas others are intermediate between the angles expected for melt and for clinopyroxene, indicating various degrees of subsolidus textural reequilibration. 3.2. Mineral chemistry Major element compositions of minerals were analysed by Cameca SX 51 electron microprobe at the University of Heidelberg. Mineral compositions correspond broadly to the observations of Ionov et al. (1993): major element analyses are given in Tables 2-7 only for minerals which were also analysed for trace elements, whereas the following brief summary is based on a larger sample set. Olivines in the Bereya peridotites are unzoned with forsterite contents from 89 to 91. The M g # (100 M g / ( M g + Fe)) is slightly higher in spinel peridotites than in garnet peridotites. On a plot of modal olivine content against M g # of olivines (Fig. 4), Bereya peridotites plot clearly in the region typical for fertile non-cratonic spinel lherzolites (Boyd,
S.M. Glaser et al. ,/Lithos 48 (1999) 263-285
269
Table 2 Major and trace element compositions of olivines Major elements by electron microprobe, trace elements by L A M - I C P - M S in Tables 2-7" n = number of analyses averaged for the L A M - I C P - M S data. wt. %
Gt-peridotite s
n
S p-peridotites
Pyroxenite
SF-93205
SG-96B 13
SF-93174
SG-96B 11
SF-93162
SF-93803
41.01 0.01 0.04 49.10 10.13 0.10 0.03 0.01 100.78
40.50
40.94 0.01 0.02 49.17 9.43 0.07 0.02 0.01 100.10
40.97 0.01 0.06 49.43 9.82 0.09 0.02
40.99
40.91
0.05 48.93 10.26 0.06 0.02
49.41 10.01 0.03
39.99 0.05 0.03 45.76 12.77 0.05
100.95
100.46
0.02 100.88
99.17
SiO 2 TiO 2 A1203 MgO FeO CaO Na20 K20 Total
ppm Cs Rb Ba Th U Nb Ta La Ce Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Li Sc V Cr Mn Co Ni Cu Zn Ga
G t - S p-peridotite s
SF-93163
7
0.01 48.29 9.84 0.05
99.12 4
0.03 0.09 0.003 0.003 0.028 0.003 0.017 0.047 0.005 0.32 0.017 0.007 0.090 0.003 0.004 0.005 < 0.003 0.009 0.027 < 0.003 0.003 < 0.003 0.005 < 0.003 2.30 20.3 6.92 184 990 152 2840
4
< < < <
116 0.63
< <
<
<
< <
0.010 0.008 0.07 0.02 0.015 0.099 0.01 0.12 0.032 0.035 0.073 0.014 0.013 0.09 0.007 0.035 0.079 0.01 0.41
< 0.08 < 0.02 2.57 8.01 253 1120 168 3230 0.89 155 1.01
2
< 0.05 < 0.08 0.003 < 0.01 < 0.05 < 0.01 0.007 0.028 < 0.01 0.025 < 0.02 < 0.05 < 0.08 0.007 < 0.01 < 0.04 < 0.01 0.014 0.020 < 0.003 < 0.25 < 0.01 0.006 < 0.003 2.42 5.36 132 1110 2640 159
7
< < < <
0.04 0.11 0.003 0.003 0.008 < 0.003 0.003 0.008 < 0.003 0.072 < 0.003 0.056 0.003 0.003 0.003 0.003 0.004 0.012 < 0.003 0.003 < 0.003 0.015 < 0.003 1.81 18.4 6.23 175 870 132 2340 < < < <
97 0.55
< 0.06 0.04 0.005 < 0.003 < 0.05 < 0.01 < 0.02 0.067 < 0.01 0.18 < 0.05 < 0.14 0.20 0.004 0.007 0.004 < 0.01 < 0.05 0.056 < 0.02 < 0.12 < 0.07 < 0.01 0.015 1.30 3.12 4.83 220 1050 95 2720 2.32 168 0.86
3
3
< < < < < < < < < < < < < < < <
0.003 0.01 0.10 0.02 0.02 0.06 0.02 0.17 0.05 0.16 0.007 0.06 0.003 0.12 0.02 0.07 0.04 0.01 0.59
< 0.09 < 0.01 2.33 4.52 1040 153 2930 1.38 130 0.90
< 0.003 0.006 <0.11 0.005 0.009 < 0.02 < 0.03 0.18 < 0.09 < 0.23 0.15 < 0.06 < 0.02 0.014 < 0.01 <0.12 < 0.10 0.009 < 0.64 <0.10 < 0.02 3.64 2.20 4.26 89 1200 181 3550 3.44 238 1.41
270
S.M. Glaser et a l . / Lithos 48 (1999) 263-285
Table 3 Major and trace element analyses of orthopyroxene wt. %
Gt-peridotites
n
Sp-peridotites
Pyroxenite
SF-93205
SG-96B 13
SF-93174
SG-96B 11
SF-93162
SF-93803
55.07 0.17 4.33 32.87 6.45 0.94 0.21
54.94 0.12 4.01 32.33 6.10 0.96 0.18 0.01 99.34
55.37 0.17 4.02 32.85 6.02 0.83 0.15
54.73 0.17 5.27 31.95 6.47 1.23 0.18 0.01 100.82
54.82 0.18 3.72 33.22 6.16 0.73 0.10 0.01 99.50
54.91 0.32 3.92 32.34 6.64 0.85 0.23
54.00 0.46 4.69 30.57 8.59 0.81 0.55 0.01 100.15
SiO 2 TiO2 A12 03 MgO FeO CaO Na20 K20 Total
ppm Cs Rb Ba Th U Nb Ta La Ce Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Li Sc V Cr Mn Co Ni Cu Zn Ga
G t - Sp-peridotites
SF-93163
100.66 3
3
< < < <
0.03 0.06 0.003 0.003 0.039 < 0.003 0.005 0.024 0.006 0.35 0.046 0.023 1.34 0.066 0.015 0.032 0.012 0.069 0.31 0.011 0.036 0.007 0.036 0.006 1.36 30.6 108 3650 960 62.7 810 73.8 6.71
1989; Menzies,
100.19 2
< 0.01 < 0.01 0.12 0.006 < 0.01 0.050 < 0.02 0.21 0.14 0.036 0.45 0.043 < 0.02 < 0.09 < 0.02 0.056 0.19 0.019 < 0.53 < 0.06 0.005 8.63 101 3370 1010 68.4 800 0.97 93.8 6.45
4
< 0.18 < 0.65 < 0.04 0.004 < 0.20 < 0.03 < 0.003 < 0.03 < 0.02 0.38 0.045 < 0.10 1.10 0.022 < 0.03 < 0.16 0.006 < 0.10 0.19 < 0.02 < 0.69 < 0.03 < 0.16 < 0.003 8.03 110 3510 1030 880 97.6
1990). The samples with the lowest
m o d a l o l i v i n e c o n t e n t s w h i c h p l o t to t h e r i g h t o f t h e
3
< 0.03 < 0.08 0.003 < 0.003 0.106 < 0.003 0.012 0.061 0.009 0.55 0.059 0.028 1.41 0.056 0.014 0.025 0.012 0.073 0.36 0.012 0.045 0.008 0.032 0.004 1.23 27.7 102 3780 910 56.4 670 61.1 6.49
99.94 2
< 0.28 <0.71 < 0.02 < 0.04 0.46 0.017 < 0.07 < 0.08 < 0.03 0.72 < 0.14 < 0.24 11.3 0.55 < 0.03 < 0.21 0.041 0.14 0.45 < 0.03 < 0.77 < 0.07 < 0.11 < 0.02 10.8 63.9 3860 1010 55.3 790 3.55 100 5.69
2
< 0.02 < 0.02 0.13 < 0.02 < 0.02 0.054 0.042 0.41 < 0.09 < 0.15 1.09 0.057 < 0.02 < 0.16 0.040 < 0.07 0.13 < 0.01 < 0.59 < 0.09 < 0.01 7.69 100 4580 890 55.8 720 1.04 68.2 6.72
s p i n e l l h e r z o l i t e f i e l d in F i g . 4 a r e
< 0.01 < 0.01 0.073 < 0.01 < 0.01 0.039 0.011 1.24 0.088 < 0.10 5.58 0.31 0.048 0.076 0.014 0.15 0.50 0.020 < 0.27 < 0.06 < 0.01 2.70 6.16 59.9 1280 780 53.5 730 2.52 91.0 9.5
"re-fertilised"
samples with high proportions of second-generation
S.M. Glaser er rrl. / Lithos 48 ( 1999) 263-285
27 1
Table 4 Major and trace element analyses of clinopyroxene
SiOz TiO, A1203 MgO FeO CaO Na, 0 K2O Total n
PPm Cs Rb Ba Th
u Nb Ta La Ce Pr Sr Nd Sm Zr Hf Eu Gd Tb
DY Y Ho Er Trn Yb Lu Li Sc
v Cr Mn Co Ni Cu
Zn Ga
clinopyroxene. Olivine in the orthopyroxenites shows clearly lower Mg# of 86-87.
Orthopyroxenes are unzoned and also have Mg# ranging between 89 and 91, correlating with the
272
S.M. Glaser et a l . / Lithos 48 (1999) 263-285
Table 5 Major and trace element analyses of garnet wt.%
Gt-peridotites SF-93163
SiO 2 TiO 2 A1203 MgO FeO CaO Na20 K20 Total n
ppm Cs Rb Ba Th U Nb Ta La Ce Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Li Sc V Cr Mn Co Ni Cu Zn Ga
Gt-Sp-peridotites SF-93205
SG-96B 13
SF-93174
41.71 0.16 23.33 20.79 7.17 4.92
42.40 0.18 22.57 21.01 7.17 4.95 0.02
43.06 0.21 22.67 21.79 7.36 4.79 0.03
99.87
99.91
101.65
42.49 0.21 22.92 21.53 7.44 4.79 0.02 0.01 100.96 4
5
< 0.04 < 0.12 < 0.003 0.003 0.13 0.008 0.004 0.066 0.030 0.18 0.39 0.58 20.7 0.42 0.37 1.30 0.51 4.20 25.4 1.03 3.30 0.49 3.36 0.51 0.15 95.8 115 10,600 2680 52.0 105 39.9 6.15
5
< 0.003 0.010 0.21 < 0.02 < 0.02 0.020 < 0.02 0.16 0.14 0.28 6.82 0.16 0.19 0.94 0.26 2.15 14.4 0.56 1.58 1.83 0.27 92.3 95.6 6720 1980 38.6 69.2 0.21 33.5 4.02
4
< < < <
0.08 0.16 0.003 0.01 0.22 < 0.01 0.013 0.067 0.023 0.15 0.23 0.37 13.0 0.24 0.23 1.05 0.30 2.40 14.5 0.56 1.71 0.23 1.52 0.21
86.8 91.1 6180 2310 47.0 31.1
< 0.08 0.103 0.005 0.007 0.20 0.006 0.019 0.12 0.036 0.24 0.39 0.59 22.5 0.45 0.34 1.32 0.46 3.75 21.8 0.84 2.54 0.35 2.25 0.34 0.13 72.0 98.2 9160 2290 44.4 70.7 27.7 4.93
M g # in coexisting olivines. Correspondingly, the M g # in the pyroxenites is 86-87. TiO 2 and Cr203
contents of orthopyroxenes are higher in spinel lherzolites than in either group of garnet-bearing peridotites, and also higher than typical spinel lherzolites from other localities around the world. The garnetbearing samples, however, are similar to fertile spinel lherzolites from non-cratonic areas. The presence or absence of phlogopite and/or amphibole in the Bereya samples does not affect this observation. Compared to the other samples orthopyroxene in the cumulate pyroxenites contains less Cr20 3 but considerably more TiO 2 (0.45-0.5 wt.%; see Table 3, sample SF-93803). Considering their varying textural relationships, clinopyroxenes in the Bereya peridotites are remarkably uniform in composition; they are diopsides with a high content of jadeiite (8.75-16.5 mol%) resulting from exceptionally high Na20 contents, which are on average higher than all known spinel lherzolite localities. TiO 2 contents decrease from the spinel peridotites (0.6-1.1 wt.%) to the garnet peridotites (0.4-0.55 wt.%). The major element chemistry of the two clinopyroxene generations has been investigated thoroughly for samples SF-93163 and SF93174, showing the second generation to have 0.40.5 wt.% higher A120 3 (averages of 6.98 vs. 6.50 wt.% for SF-93174) and marginally lower M g # (minimum of 88.2 vs. 88.9 in SF-93163), but to be otherwise essentially indistinguishable. Garnets in the Bereya xenoliths are generally homogenous and pyrope-rich, with low contents of almandine, grossular and spessartine. Garnets in the garnet lherzolites have higher contents of CaO (5.22 vs. 4.75 wt.%) and Cr20 3 (1.5 vs. 1.05 wt.%) than in garnet-spinel lherzolites. Spinels are also uniform in composition, consisting of 54-61 mol% Mg-spinel, 15-18% hercynite, 15-21% Mg-chromite and 3-6% Fe-chromite. There are no significant differences in composition between spinel relicts in garnet and those which appear as individual grains, with the exception of two samples: spinel in the harzburgite sample SG-96B 11 is richer in chromite component (30 mol%), while in sample SF-93163 (garnet lherzolite) the Mg-spinel component makes up 65 mol%. Spinels in kelyphites (Kp-2) are richer in A120 3 than primary spinels. Pargasitic amphibole occurring as inclusions in other silicate minerals in the spinel harzburgite has a higher M g # (87), lower TiO 2 and higher K20 than
S.M. Glaser et al. / Lithos 48 (1999) 263-285
273
Table 6 Major and trace element analyses of spinel wt.%
Gt-Sp-peridotites
Sp-peridotites
SF-93163
SF-93205
SG-96B 13
SG-96B11
SF-93162
SiO 2 TiO 2 A1203 Cr20 3 MgO FeO CaO
0.11 0.36 45.98 19.33 18.63 13.36 0.02
0.02 0.35 43.97 22.72 18.55 13.26
0.08 0.47 43.74 22.52 18.51 13.71 0.02
0.07 1.09 37.64 26.30 17.22 16.10 0.04
0.06 0.39 45.10 20.61 18.46 13.64
Na20 K20 Total
0.01 97.89
0.01 99.15
0.01 98.61
n ppm Cs Rb Ba Th U Nb Ta La Ce Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Li Sc V Mn Co Ni Cu Zn Ga
Gt-peridotites
3
99.35 2
< < < <
0.28 0.55 0.003 0.003 1.18 0.008 0.004 0.004 < 0.003 0.17 0.021 < 0.003 0.80 0.018 < 0.003 0.004 < 0.02 0.009 0.046 < 0.003 0.013 0.003 < 0.09 0.005 0.61 7.46 687 1070 252 3150 1350 139
3
0.002 < 0.002 1.28 0.069 < 0.003 0.072 0.032 0.20 < 0.003 < 0.003 3.31 < 0.01 < 0.003 0.45 0.021 0.008 0.095 0.003 < 0.003 < 0.03 0.052 1.21 694 950 418 2730 8.69 1870 116
3
< 0.25 < 0.64 0.021 0.008 4.59 < 0.11 < 0.07 < 0.06 < 0.06 0.29 0.092 0.077 2.87 0.46 < 0.07 0.039 < 0.04 < 0.21 0.061 < 0.03 < 2.02 < 0.06 < 0.40 < 0.03 < 1.98 666 1050 2600 2310
in the pyroxenite (Mg# = 83). Both are enriched in Cr203 and K20 relative to the vein amphiboles
98.42 2
< 0.49 < 0.02 < 0.04 0.018 < 0.003 3.98 < 0.01 < 0.003 0.017 < 0.003 < 0.78 < 0.02 < 0.02 3.35 0.12 < 0.003 < 0.03 < 0.003 < 0.02 < 0.01 < 0.017 < 0.15 < 0.01 < 0.02 < 0.003 < 0.11 481 1110 254 3960 21.9 2810 97.9
< 0.04 < 0.07 2.91 < 0.07 < 0.06 < 0.10 < 0.12 0.66 < 0.16 < 0.20 3.05 0.11 < 0.07 < 0.50 < 0.05 < 0.25 < 0.07 < 0.064 < 1.68 < 0.27 < 0.03 < 1.41 768 1190 273 3240 20.3 1950 146
described by Ionov et al. (1993). Phlogopites occur rarely but are represented in all peridotite groups in
S.M. Glaser et ul. / Lithos 48 (1999) 263-285
274
Table 7 Major and trace element analyses of amphibole and phlogopite wt.%
Amphibole
Pyroxenite
Sp-Lhz
Gt-Sp-Lhz
Pyroxenite
SG-96B 11
SF-93803
SG-96B11
SG-96B 13
5 F-93803
41.76 4.38 13.76 16.23 5.88 8.41 3.58 1.26 96.2 1
38.08 4.60 15.11 19.91 4.57 0.30 0.49 7.54 92.22
38.46 4.62 15.88 20.23 4.31 0.03 0.4 1 9.65 95.15
35.66 6.57 16.21 18.63 6.53 0.04 1.16 8.06 93.56
SiO,
42.87 3.41 13.24 16.62 4.45 9.78 3.02 2.13 97.33
TiO, A1203
MgO FeO CaO Na,O K2O Total n
Phlogopite
Sp-Lhz
5
2
3
3
1
ppm
cs
Rb Ba Th U Nb Ta La Ce Pr Sr Nd
Sm Zr Hf
ELI Gd Tb DY Y Ho Er Tm Yb Lu Li
sc V Cr Mn co Ni
cu Zn Ga
1.31
5.95 79.5 0.072 0.014 53.5 5.23 2.23 9.98 1.79 214 9.60 3.53 191 8.26 1.23 3.13 0.44 2.17 6.8 1 0.28 0.58 0.059 0.34 0.040 29.5 244 10,300 430 35.4 814 14.5 45.1 20.9
0.034 0.012 15.9 1.33 2.22 10.3 I .88 249 10.8 3.36 98.8 4.85 1.28 3.35 0.54 2.55 9.04 0.40 0.79 0.32 0.032 1.16 15.9 219 4200 506 42.0 829 16.0 52.8 28.0
154 824 < 0.04 < 0.02 34.4 3.06 0.52
77.5
< 0.18 < 0.22 28.1 0.78 < 0.05 < 0.30 < 0.05 0.78
< 1.01 < 0.25 7.70 4.42 199 9730 176 63.1 2090 13.7 80.2 177
41.4 43 1 < 0.02 0.010 22.4 0.66 0.15 < 0.02 < 0.03 45.9 < 0.14 < 0.17 3.92 0.21 < 0.04 0.1 1 0.006 < 0.07 0.35 < 0.02 < 0.90 < 0.03 0.084 < 0.003 3.77 387 9040 170 1660 66.9
0.003 0.090 4.1 0.50 < 0.10 0.19 < 0.03 91 .8 < 0.06 < 0.14 6.00 0.36 0.056 0.28 < 0.05 < 0.11 1.36 < 0.02 < 0.49
< 0.13 < 0.03 3.85 2.70 181 2440 161 63.8 1910 7.62 68.0 310
S.M. Glaser et al./Lithos 48 (1999) 263-285
95 94 93 92 o 91
%
;~ 90
m
89 88 100
n 90
80
70
60
50
40
Modal % olivine Fig. 4. Relation between M g # of olivine and modal olivine content in peridotites from various areas. The Bereya samples (filled circles) fall mostly within the field characteristic for fertile spinel lherzolites (diagonally shaded field = Proterozoic samples after Menzies, 1990) and are distinct from the field of Kaapvaal cratonic peridotites, which are offset to higher M g # at similar modal olivine contents (grey shading; Boyd, 1989). Depleted peridotites of Tanzania (Lashaine = squares, Olmani = open circles; Rudnick et al., 1994) and West Greenland (cross-hatch; Bernstein et al., 1998) lie to higher M g # and modal olivine contents.
Bereya. Peridotitic phlogopites contain less TiO 2 but more Cr20 3 than those in the pyroxenite (Table 7) and have higher M g # (89 vs. 84). 3.3. Pressure and temperature estimates for the peridotites
The infiltration of the peridotites by a silicate melt within the mantle and the resulting disequilibrium between major mineral phases poses problems for the selection of suitable thermometers and barometers. We have, therefore, compared the results from several thermometers, including (1) Ca-in-orthopyroxene, (2) Na exchange between pyroxenes, and (3) the commonly used "two-pyroxene" thermometer (diopside (Di)-enstatite (En) exchange between clinopyroxene and orthopyroxene). All formulations were those of Brey and KiShler (1990). Pressure was estimated by the orthopyroxene/garnet A120 3 exchange barometer of Brey and KiShler (1990) for garnet-bearing samples, and by the Cr-in-spinel
275
barometer of Webb and Wood (1986) for spinelbearing samples. The latter barometer permits estimates for garnet-free samples from Bereya by elimination of Cr in garnet from the calculation. The results give P - T estimates of 20-23 kbar and 1024~ - 1087~ for the garnet lherzolites, 20-21 kbar and 1000~ - 1034~ for the garnet-spinel lherzolites, and 20-22 kbar and 1005~ - 1090~ for the spinel lherzolites. The results for the garnet-bearing samples are similar to the range of 16.5-22.5 kbar and 990~176 given by Ionov et al. (1993), and are all very close to the transition depth between spinel and garnet lherzolites. Similar depths for all xenolith types are also suggested by the occurrence of composite xenoliths (Ionov et al., 1993). A much larger pressure range of 18-30 kbar is given by Ashchepkov et al. (1994) and Litasov and Litasov (1999) on the basis of a more extensive sample collection, although using different thermobarometers. The most reliable temperature estimates came from the Ca-in-orthopyroxene thermometer, probably because it does not consult the composition of the coexisting clinopyroxene which was disturbed or even fully introduced during the melt infiltration event. The Na-thermometer overestimates temperatures by variable amounts up to 300~ which result in absurdly high pressure estimates (up to 15 kbar too high) when combined with barometers. The DiEn thermometer also overestimates temperatures, but to a lesser extent (generally < 130~ The overestimation by both thermometers using the clinopyroxene composition is considered to indicate disequilibrium between the pyroxenes, which finds its textural expression in Fig. 3c-f. The temperatures for the sheared lherzolite (1005~ by Ca-in-orthopyroxene) are severely underestimated by the other two thermometers (620~ by the Di-En exchange thermometer). The reason for this is not clear, but it cannot be a simple function of the high jadeite contents, which are also higher in other Bereya samples relative to peridotites from other areas. In contrast to a sheared peridotite reported by Ashchepkov et al. (1994) and to sheared garnet peridotites sampled by kimberlites (Nickel and Green, 1985), the temperature estimates for the sheared sample are not higher than for undeformed samples.
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4. Trace element chemistry of minerals Seven samples were selected for trace element analysis by Laser Ablation Microprobe (LAM-ICPMS) to provide representative information on the trace element behaviour of each of the three xenolith groups. These seven samples include two with textural evidence for melt infiltration, the sheared xenolith SF-93162, and an amphibole- or phlogopite-bearing example of each group, where available. The Laser-ICP-MS system used was that at the ETH in Ziirich, Switzerland, which consists of an Excimer laser coupled to a Perkin-Elmer ELAN 6000 ICP-MS (Giinther et al., 1997). The ICP-MS is equipped with a dual detector mode, allowing simultaneous detection of major and trace elements, so that almost all major elements were monitored during analysis of a trace element palette of up to 40 elements. The prototype excimer laser (5% F in Ar, 193 nm) beam is homogenised, allowing very homogeneous laser illumination of the sample surface and control of the ablation process. Fractionation effects are reduced to an insignificant amount by the photoionisation-dominated ablation process, so that accuracy is better than 5% even for highly fractionating elements. This is especially valuable for the more volatile compatible trace elements such as Zn and Ga. Reproducibility is sample-dominated; 10 replicates on homogeneous test samples allow relative standard deviations of 1-3% for most of the elements. Signal correlation between volatile and refractory elements shows no significant fractionation effects until ablation pit depth exceeds pit diameter. This posed no problem for the analyses presented here, which were performed with pit diameters of 40-80 lxm on marginally thick polished thin sections using pulse energies of 120-200 mJ and a repetition rate of 10 Hz. The analyses were standardised externally on NIST 610 and 612 glasses, and internally on electron probe analyses of Si for silicate phases and A1 for spinels. For data acquisition parameters and data reduction procedure used for the calculation of concentrations and limits of detection see Longerich et al. (1996). We have analyzed incompatible (ITE) as well as compatible (CTE) trace elements in all constituent phases (olivine, orthopyroxene, clinopyroxene, garnet, spinel, amphibole and phlogopite). As a result of
the optimized laser system we can present a more complete set of partitioning data for minerals with very low concentrations of many trace elements (e.g., spinel and orthopyroxene), and for mineral pairs (e.g., garnet/spinel) than was previously possible using in situ techniques. Results are listed in Tables 2-7 for individual minerals and illustrated in Figs. 5-7. Arsenic is not listed in the tables as it was detected only in one spinel in a garnet lherzolite at a level of 0.12 ppm. The limits of detection for all other measured isotopes are in the very low 1-10 ppb region even for a spatial resolution of 40 Ixm. These low limits of detection are mainly due to changes in the carrier gas composition leading to increased sensitivity and reduced background intensities. A 300 ml/min helium carrier gas flow through the ablation cell was mixed with argon in front of the ICP-MS to maintain the total gas flow at an optimum level (Giinther and Heinrich, 1998). For Li almost no background counts have been detected resulting in greatly improved detection capabilities for elements with low atomic mass. 4.1. Incompatible trace elements
ITE abundances are illustrated in Fig. 5 for orthopyroxene, clinopyroxene, garnet and amphibole. No plots are presented for olivine, spinel and phlogopite as the patterns are incomplete despite the very low limits of detection of the Laser-ICP-MS. Fig. 5a compares the patterns for the Bereya orthopyroxenes to a pattern for an orthopyroxene mineral separate from a xenolith from the Baikal Rift-related Tariat volcanic field in Mongolia (Ionov and Hofmann, 1995) and to a Laser-ICP-MS analysis from a spinel lherzolite from southeastern Australia (Eggins et al., 1998). Although the patterns are generally similar, the abundances of Nb, Ta and Th detected in the Bereya samples are significantly higher than in the pattems for the other two localities. The patterns for gamet also show higher abundances for elements to the left of La in Fig. 5c than are expected from experimentally determined partition coefficients (Green, 1994). In contrast, the patterns for clinopyroxene and amphibole (Fig. 5b and d) generally correspond to those expected for these minerals in peridotites. The ITE patterns are interpreted as showing variable degrees of approach to
(a)
Opx
i-1
o
0,1
t~
,,
[
,
.
] 4~ O~ -
t',o I
+
---0--
I
t
Fig. 5. Incompatible trace elements in minerals from Bereya peridotites normalised to primitive mantle using values given by Sun and McDonough (1989). (a) Orthopyroxene: overall levels are typical for peridotitic orthopyroxene for the less incompatible elements (right of diagram) but the more incompatible elements (left) are unusually enriched indicating partial re-equilibration with infiltrating melt. The Tariat sample ( + ; Ionov and Hofmann, 1995) is also from the Baikal region (see Fig. 1) but does not show this enrichment. The solid line indicates Opx from spinel lherzolites from southeastern Australia (Eggins et al., 1998). Only samples where 12 or more ITE were detected are plotted. (b) Clinopyroxene patterns are notable for inconsistent behaviour of HFSE. (c) Garnets show normal patterns to the right of Sr, but unusual enrichments to the left, indicating partial re-equilibration with infiltrating melt. (d) Amphiboles differ from those of Bartoy (Ionov and Hofmann, 1995; see Fig. 1), with lower HREE and higher HFSE, reversing the sense of the anomaly for Zr and Hf.
O~ k~
278
S.M. Glaser et a l . / Lithos 48 (1999) 263-285
~
I
l
t
I
I
=
~
~
~
z
b
t
I
~- -~ 8
I
t
t
t
t
i
k
~- ~
i
~
~
~
~
~
~
I
t
I
l
i
t
t
~'
Fig. 6. Amphibole/clinopyroxene partitioning of trace elements, showing similar patterns for Bereya to those for Kakanui garnet pyroxenites (Zack et al., 1997) and Bartoy xenoliths (Ionov and Hofmann, 1995). Similarity of patterns is evidence for ITE equilibrium between these two phases in the Bereya peridotites.
equilibrium for ITE in different minerals, whereby only the strongly incompatible elements in orthopyroxene and garnet have responded to the infiltrating melt. The degree of re-equilibration is much greater for clinopyroxene and amphibole, and amphibole/ clinopyroxene partitioning is similar to that found in other areas (Fig. 6) supporting the interpretation that these two minerals are in ITE equilibrium with each other. The ITE patterns for clinopyroxene and amphibole are also noteworthy for the behaviour of Nb, Ta, Zr and Hf. Most clinopyroxenes show a trough in the pattern at Zr and Hf, which is a well-known feature of peridotitic clinopyroxenes (Salters and Shimizu, 1988; Rampone et al., 1991), whereas SG96B 11 shows positive anomalies for Zr, Hf and even Ta (Fig. 5c). Both the analysed amphiboles (from spinel harzburgite SG-96B 11 and the pyroxenite SF93803) show strong positive anomalies in the pattern at Z r - H f and Nb-Ta. The Z r - H f anomalies are not evident in amphiboles analysed by Ionov and Hofmann (1995) from Bartoy, whereas the ratios amphibole/clinopyroxene shown in Fig. 6 are very similar to those from Bartoy and to garnet clinopyroxenites from Kakanui in New Zealand (Zack et al., 1997). The improved Laser-ICP-MS system allowed analysis of Li in several phases. The results confirm those of Ottolini and McDonough (1996) that olivine
is more enriched in Li than the pyroxenes and spinel, but add the observation that phlogopite would be more enriched in Li than olivine in hydrous mantle peridotites, albeit marginally. The Bereya phlogopites show significantly lower L i / N b than those analysed in natural lamprophyres (Foley et al., 1996) or in experimental partitioning studies (Schmidt et al., 1998); olivine was not present in either of the latter studies. Spinel analyses show very low levels of most ITEs (0.01-0.2 times primitive mantle) but appreciably more of the high field strength elements (HFSE), and are consistent with other data for low-Ti spinels (Stosch, 1982; Horn et al., 1994). 4.2. Compatible trace elements
The Excimer Laser-ICP-MS system enabled the analysis of an extensive data set for CTE in all phases in the xenoliths. The values of Mn, Cr and Ni are comparable with those measured by microprobe (e.g., Ni in SG-96B 11:2720 ppm by LAM vs. 3080 by EMP; in SF-93162:2930 vs. 3070; in SF-93163: 2840 vs. 2860). Values for the CTE are also given in Tables 2-7, and their relative concentrations in the mineral phases are illustrated in Fig. 7. Previous data sets have analyses for fewer CTE, and very few of them include garnet-bearing lherzolites (Stosch, 1981; Luhr and Aranda-G6mez, 1997; Qu et al.,
279
S.M. Glaser et al./Lithos 48 (1999) 263-285
BGrt
[] []
),.. :. ..,.. i...: "
ii!:i:..::.:
I"~ "" '~ ~"~ ~•'q
~'~ 1!~~ .... ,_,.,
~
,
'"" "'" ~~.'~'~ i" ,,-..,.~
u...'
Fig. 7. Distribution of compatible trace elements between the phases of representative Bereya garnet lherzolites (SF-93205), garnet-spinel lherzolites (SG-96B 13) and spinel harzburgite SG-96B 11. The latter two samples also contain hydrous phases. Garnet is the main carrier for Sc and marginally so for Mn. Spinel is the dominant carrier of Cr, Co and Zn, and also for Ga in the absence of phlogopite.
280
S.M. Glaser et a l . / Lithos 48 (1999) 263-285
1997; Eggins et al., 1998). In making comparisons it must be remembered that the constituent minerals of the Bereya peridotites are not all in equilibrium with each other, and that partitioning of many of these elements is known to be a strong function of temperature, so that the temperature recorded by these xenoliths (1050 _+ 50~ must be taken into account. Fig. 7 shows that in garnet lherzolite SF-93205 garnet has the highest concentrations of Sc, whereas spinel dominates V, Cr, Co, Zn and Ga. Appreciable concentrations of Mn are found in all lherzolite phases, but are highest in garnet, where present. Ni is carried by olivine and spinel in approximately equal amounts (3230 vs. 2730 ppm), whereby olivine dominates the total Ni budget due to its high modal abundance. The DNi (ol/opx) varies between 3.5 and 4.0 for the garnet peridotites and between 1.75 and 4.1 (average 3.53) for the whole lherzolite suite. Minerals have the aptitude to greatly influence element budgets in rocks where they are not major constituents only where the primitive mantle-normalised concentrations of these CTE are greater than about five. This is not the case for any CTE in either clino- or orthopyroxene, and is only marginally the case for Ni in olivine, Sc in garnet, and Ga in amphibole. Ga in phlogopite, and Zn, Ga, Cr and possibly V in spinel, however, can have 10-100 times the concentration of primitive mantle, so they cannot be neglected even when present in very small amounts. The takeup of V in spinel is a strong function of oxygen fugacity because V 3+ can be easily accommodated in spinel, whereas V 5+, which predominates under oxidising conditions, is incompatible in spinel (Horn et al., 1994). Calculation of the oxygen fugacity in Bereya peridotites gives values of FMQ to FMQ- 1 (Ballhaus et al., 1991; Ionov and Wood, 1992), corresponding to DV (sp/cpx) in the range 2.2-2.6 (Horn et al., 1994). The Bereya peridotites also provide a rare opportunity to assemble a partitioning database for both ITE and CTE between coexisting garnet and spinel. Spinel contains very low abundances of ITE, resulting in a pattern for gt/sp resembling that of garnet. No anomaly is seen at Zr despite the preferential incorporation of Zr in spinel relative to the neighbouring ITEs because garnet also shows a small positive anomaly in its pattern (Fig. 5c).
5. Discussion
5.1. The melt infiltration event in the Bereya peridotites The Bereya lherzolite sample suite studied here contains more evidence for trace element enrichment by melt infiltration within the mantle than described by Ionov et al. (1993) for samples from this locality. The combination of in situ trace element analyses of minerals with petrographic observations and major element chemistry permit the relative timing and conditions of the infiltration event to be defined, and also the nature of the infiltrating melt. This information helps to delineate the development of the mantle beneath the evolving Baikal rift. The petrographically observed textures, including clinopyroxene networks which mimic melt morphologies (Fig. 3c-f) demonstrate the later crystallisation of clinopyroxene relative to garnets, spinels and many olivines and orthopyroxenes, and that the clinopyroxene crystallised from an infiltrating melt. Given this evidence for strong textural disequilibrium, it may be suspected that chemical equilibration between previously existing minerals and the infiltrating melt was also not reached and that disequilibrium partitioning occurs. There are several indications for only a partial attainment of equilibrium: (1) the anomalously high contents of the most incompatible elements in orthopyroxenes and especially garnets (Fig. 5a and c) may indicate that these minerals were affected by the infiltrating melt but that equilibrium was not reached; (2) the patterns for clinopyroxene (Fig. 5b) and amphibole (Fig. 5d) lack the anomalous relative enrichment in the strongly incompatible elements, being consistent instead with equilibrium trace element distribution with the melt and with each other (Fig. 6); (3) the application of thermobarometers incorporating clinopyroxene compositions result in misleading temperature estimates, whereas those made using only orthopyroxene are probably realistic. We interpret these features as indicating that the ITE abundances in orthopyroxene and garnet show some effects of interaction with the infiltrating melt, whereas their major and CTE abundances are largely unaffected. There is some evidence for the existence of an earlier clinopyroxene generation in the form of
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S.M. Glaser et al. / Lithos 48 (1999) 263-285
volcanic field (Ionov and Hofmann, 1995). The calculated melt from all three clinopyroxenes is similar to the natural volcanic patterns, whereas that for the amphibole deviates strongly for the HFSE. However, this is not due the use of inappropriate partition coefficients for these elements, which can be expected to vary as a function of the Ti-content of the melt (Tiepolo et al., 1998), but is a characteristic of sample S G - 9 6 B l l ; a similar pattern results when calculated from clinopyroxene. The sample-specificity of the positive anomaly for HFSE implies a very local effect, which is reminiscent of the extremely variable Zr concentrations found in clinopyroxenes of the Inagli complex, Siberia, by Zinngrebe et al. (1995). These authors attributed positive Zr anomalies to local reaction between infiltrating melt and spinels in the host ultramafic rocks. The anomaly is caused by the uptake of A120 3 from spinel by the infiltrating melt which thus loses its peralkaline nature. In moving from peralkaline to subalkaline melt compositions the solubility of Zr in the melt drops sharply due to the elimination of alkali-Zr-silicate complexes which are only stable in peralkaline conditions (Watson and Harrison, 1983). The Bereya sample which shows the positive HFSE anomalies has the highest modal spinel (1.3 vol.%) and lowest
minor zonation in A I 2 0 3 and M g # and also in zonation of ITE towards patterns more enriched in all ITE (these rare analyses are not included in the averages in Table 4 or in Fig. 5b). However, even the earliest clinopyroxenes are unlikely to represent unchanged, pre-infiltration compositions, as indicated by the failure of the thermometers. Thus, the apparently very fertile compositions of the Bereya peridotites (Fig. 4, Table 1) may be at least partly due to secondary introduction of melt components. We have attempted to reconstruct the chemical identity of the infiltrating melt via experimental mine r a l / m e l t partitioning. This method assumes equilibrium between minerals currently found in the peridotite and the infiltrating melt, and that their ITE partitioning follows that determined in experimental work. This method must be considered crude in view of possible subsolidus re-equilibration of the ITE (Rampone et al., 1993; Eggins et al., 1998), but the preservation of ITE zonation justifies it as a firstorder calculation. Results of such calculations based on clinopyroxene from three samples and amphibole from a fourth are shown in Fig. 8 together with the trace element pattern for the host Miocene alkali picrite tuff (Esin et al., 1995) and a Quaternary basalt from the Vitim
II I
i
I
Fig. 8. Estimated ITE patterns of the infiltrating melt calculated by assuming that clinopyroxene and amphibole ITE-contents represent equilibrium values coexisting with the infiltrating melt. Patterns for cpx are obtained via mineral/melt partition coefficients after Watson et al. (1987), Adam et al. (1993), Hart and Dunn (1993), Jenner et al. (1993), Dalp~ and Baker (1994), and Foley et al. (1996) as summarised by Zack et al. (1997), and amphibole after Zack et al. (1997). The pattern for the Bereya alkali picrite tuff is from the work of Esin et al. (1995), but may be suspected for some elements (e.g., Ba, Sr) due to the difficulty of obtaining fresh samples. However, this and an additional Vitim basalt from the Kandidushka volcano (sample 302-36; Ionov and Hofmann, 1995) show that the overall pattern for the melts calculated from Cpx is similar to that of volcanics from the same region. The pattern calculated from amphibole (B11) has positive anomalies which are characteristic of this sample (also Cpx) and not due to calculation via inappropriate partition coefficients.
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modal clinopyroxene (0.5 vol.%) contents of any of the studied samples (Table 1) and so may represent the earlier stages of melt infiltration which are more likely to show strong effects of reaction with the host rock. The similarity between the melt patterns calculated from clinopyroxene in Fig. 8 to the alkali picrite host indicates that the infiltrating melt may be related genetically to the host melt, and probably represents a marginally earlier stage in the history of the developing rift. The occurrence of rare ITE-richer zones in clinopyroxene probably indicate that the infiltrating melt was a lower-degree melt with peralkaline chemistry relative to the host alkali picrite.
5.2. Timing of events and the development of the Baikal Rift The petrographic and mineral chemical information obtained from the Bereya peridotites allows delineation of events within the mantle at the southeast flank of the developing rift before the eruption event at 16 Ma. The effect of the rifting process within the mantle will have comprised a progressive upward and outward movement of the lithosphere/asthenosphere boundary, which was accompanied by the episodic infiltration of melts into the subcrustal lithosphere and their reactivation shortly afterwards by progressive development of the rift. The following series of events can be inferred from features in the peridotites. (1) The peridotites underwent a reaction which formed garnet at the expense of spinel and pyroxenes, which is explainable by a near-isobaric cooling at pressures of 20-25 kbar. This may represent the lithosphere-forming event or possibly a later cooling event following perturbation of normal thermal conditions, but is in either case likely to pre-date the activity of the Baikal Rift. (2) The outer reaction coronas around garnets (designated Kp-2 above) indicate a later heating event which we interpret as rift-related heating due to progressive upward and outward migration of the asthenosphere/lithosphere boundary between 30 and 15 Ma. The Kp-2 reaction coronas occasionally occur between the more continuous Kp-1 and the recrystallised rims of Cpx-2 clinopyroxenes. The latter two features are interpreted to have formed during
uplift to the Earth's surface, whereas the Kp-2 rims must have existed prior to this, and most probably before the formation of Cpx-2 from the infiltrating melt. Furthermore, the mineralogy of the kelyphite indicates a reversal of the garnet-building reaction mentioned above, and implies Kp-2 kelyphite formation by a heating event in isochemical conditions, which is consistent with the upward and outward migration of the rift margin within the upper mantle. (3) The melt infiltration event demonstrated by the textures in Fig. 3c-f post-dated the rift-related heating event indicated by the Kp-2 kelyphites, and was, therefore, directly related to heating at the flanks of the developing rift. The textures shown in Fig. 3e-f must be short lived: although the timescales for the attainment of textural equilibrium are controversial, the timescale for the elimination of the low angle-texture in Fig. 3e-f would certainly be less than 0.2 Ma, indicating melt infiltration very shortly before transport of the peridotites to the Earth's surface. The peralkaline and ITE-rich chemistry of the melt inferred from the calculations presented above is consistent with its origin from the migrating rift within the mantle. Shortly after this melt infiltration, remelting of the enriched peridotites by a further heating event produced the alkali picrite melt which now hosts the peridotites at Bereya.
5.3. Comparison of non-cratonic and cratonic peridotites The results presented here on the garnet-bearing peridotites from Bereya underline the general conclusion of Ionov et al. (1993) that the upper mantle in the garnet peridotite field in this non-cratonic, rift-related setting is distinct from that seen under cratonic regions in either South Africa or Siberia. The Bereya peridotites are fertile, with high modal abundances of clinopyroxene and garnet, and the relation between M g # of olivine and modal olivine content is consistent with variable but limited depletion by loss of a basaltic melt fraction (Fig. 4). This conclusion is little modified by subsequent crystallisation of secondary clinopyroxene. The Bereya peridotites do not show a correlation between Ni content in olivine and modal orthopyroxene which is charac-
S.M. Glaser et al./Lithos 48 (1999) 263-285
teristic of Kaapvaal cratonic lherzolites (Kelemen and Hart, 1996; Boyd, 1997). Sheared lherzolite SF-93162 illustrates further differences between the Bereya peridotites and their cratonic counterparts: this xenolith exhibits a mosaic texture (Fig. 4b) but does not show the fluidal mosaic texture typical of sheared peridotites from cratonic regions (Boullier and Nicolas, 1975). Moreover, thermobarometric estimates do not deviate from those of the granular peridotites. Taken together, these points may indicate a different origin of the shearing as unrelated to the movement of magma or diapirs in the mantle, to which kimberlitic sheared xenoliths are often attributed (e.g., Ehrenberg, 1979; Mercier, 1979). Maybe this xenolith is an example of "cold" shearing related to the widening of the rift at its flanks, and thus similar to the origin originally suggested for kimberlitic sheared xenoliths (Nixon et al., 1973) but which subsequently fell out of favour.
Acknowledgements The xenoliths described here were collected by the authors in 1993 and 1996 during fieldwork orchestrated by Igor Ashchepkov. Financial assistance for the fieldwork was provided by the Deutsche Forschungsgemeinschaft (Fo 181/3-1/3-2). We are grateful to S. Schmidberger and W.F. McDonough for reviews of the manuscript, and to K. Litasov, I. Ashchepkov, E. Zinngrebe, D. Ionov, M. Drury, U. Faul and H. Green for fruitful discussions and comments. Bill McDonough is also thanked for generously sharing his database on peridotitic xenoliths.
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G., Seck, H.A., 1993. Garnet peridotite xenoliths from the Vitim volcanic field, Baikal region: the nature of the garnetspinel peridotite transition zone in the continental mantle. Journal of Petrology 34, 1141-1175. Jenner, G.A., Foley, S.F., Jackson, S.E., Green, T.H., Fryer, B.J., Longerich, H.P., 1993. Determination of partition coefficients for trace elements in high pressure-temperature experimental run products by laser ablation microprobe-inductively coupled plasma-mass spectrometry (LAM-ICP-MS). Geochimica et Cosmochimica Acta 57, 5099-5103. Kelemen, P.B., Hart, S.R., 1996. Silica enrichment in the continental lithosphere via melt/rock interaction. Journal of Conference Abstracts 1,308. Kiselev, A.I., 1987. Volcanism of the Baikal Rift zone. Tectonophysics 142, 235-244. Kiselev, A.I., Popov, A.M., 1992. Asthenospheric diapir beneath the Baikal Rift: petrological constraints. Tectonophysics 208, 287-295. Litasov, K.D., Litasov, Yu.D., 1999. Evolution of mantle magmatism beneath the Vitim volcanic field (East Siberia). Proceedings of the Seventh International Kimberlite Conference. In press. Logatchev, N.A., Zorin, Y.A., 1992. Baikal Rift zone: structure and geodynamics. Tectonophysics 208, 273-286. Longerich, H.P., Jackson, S.E., Giinther, D., 1996. Laser ablation inductively coupled plasma mass spectrometric transient signal data acquisition and analyte concentration calculation. Journal of Analytical Atomic Spectrometry 11,899-904. Luhr, J.F., Aranda-G6mez, J.J., 1997. Mexican peridotite xenoliths and tectonic terranes: correlations among vent location, texture, temperature, pressure, and oxygen fugacity. Journal of Petrology 38, 1075-1112. Menzies, M., 1983. Mantle ultramafic xenoliths in alkaline magmas: evidence for mantle heterogeneity modified by magmatic activity. In: Hawkesworth, C.J., Norry, M.J. (Eds.), Continental Basalts and Mantle Xenoliths. Shiva, Nantwich, pp. 92-110. Menzies, M., 1990. Archean, Proterozoic and Phanerozoic lithospheres. In: Menzies, M.A. (Ed.), Continental Mantle. Oxford Monographs 16, Oxford Science Publications, pp. 67-86. Mercier, J.-C., 1979. Peridotite xenoliths and the dynamics of kimberlite intrusion. In: Boyd, F.R., Meyer, H.O.A. (Eds.), The Mantle Sample: Inclusions in Kimberlites and Other Volcanics. American Geophysical Union, Washington, pp. 197-212. Mercier, J.-C., Nicolas, A., 1975. Textures and fabrics of upper mantle peridotites as illustrated by xenoliths from basalts. Journal of Petrology 16, 454-487. Nickel, K.G., Green, D.H., 1985. Empirical geothermobarometry for garnet peridotites and implications for the nature of the lithosphere, kimberlites and diamonds. Earth and Planetary Science Letters 73, 158-170. Nixon, P.H., 1987. Mantle Xenoliths. Wiley, New York, 844 pp. Nixon, P.H., Boyd, F.R., Boullier, A.-M., 1973. The evidence of kimberlite and its inclusions on the constitution of the outer part of the Earth. In: Nixon, P.H. (Ed.), Lesotho Kimberlites. Lesotho National Development, Maseru, pp. 312-318.
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LITHOS ELSEVIER
Lithos 48 (1999) 287-316
Growth of subcontinental lithosphere" evidence from repeated dike injections in the Balmuccia lherzolite massif, Italian Alps Samuel B. Mukasa
a,*,
John W. Shervais b
a Department of Geological Sciences, University of Michigan, 2534 C.C. Little Bldg., Ann Arbor, M148109-1063, USA b Department of Geological Sciences, University of South Carolina, Columbia, SC 29028, USA
Abstract
The Balmuccia alpine lherzolite massif is a fragment of subcontinental lithospheric mantle emplaced into the lower crust 251 Ma ago during the final, extensional phase of the Hercynian orogeny. The Balmuccia massif consists largely of lherzolite, with subordinate harzburgite and dunite, and an array of dike rocks formed in the mantle before crustal emplacement. Dike rocks include websterite and bronzitite of the Cr-diopside suite, spinel clinopyroxenite and spinel-poor websterite of the Al-augite suite, gabbro and gabbronorite of the late gabbro suite, and hornblendite of the hydrous vein suite. The dike rocks display consistent intrusive relationships with one another, such that Cr-diopside suite dikes are always older than dikes and veins of the Al-augite suite, followed by dikes of the late gabbro suite and veins of the hydrous vein suite. Phlogopite (phl) veinlets that formed during interaction with the adjacent crust are the youngest event. There are at least three generations of Cr-diopside suite dikes, as shown by crosscutting relations. Dikes of the Al-augite suite form a polybaric fractionation series from spinel clinopyroxenite to websterite and feldspathic websterite, which crystallized from aluminous alkaline magmas at relatively high pressures. The late gabbro suite of dikes intruded at lower pressures, where plagioclase saturation occurred before significant mafic phase fractionation. Hornblendite veins have distinct compositional and isotopic characteristics, which show that they are not related to either the Al-augite suite or to the late gabbro dike suite. Cr-diopside suite dikes have Nd and Sr isotopic compositions similar to those of the host lherzolite and within the range of compositions defined by ocean-island basalts. The Al-augite dikes and the hornblendite veins have Sr and Nd isotopic compositions similar to those of Cr-diopside suite lherzolite and websterite. The late gabbro dikes have Nd and Sr isotopic compositions similar to mid-ocean ridge basalt (MORB) asthenosphere. Lead isotopic compositions for all of the samples fall in the present-day MORB field on the 2~176 vs. 2~176 diagram but are displaced above this field on the 2~176 vs. 2~176 diagram. There is overlap in the data between the Cr-diopside suite and the Al-augite and hydrous vein suites, with the exception that the Cr-diopside websterite dikes have more radiogenic Pb than any of the other samples. In Pb-Pb space as well, the late gabbro suite has the least radiogenic isotopic compositions, reflecting a change in magma source region during uplift. These data show that tectonic thinning of subcontinental lithospheric mantle during extension caused a change in the source regions of mantle-derived magmas from an ocean island basalt (OIB)-like lithosphere to the underlying MORB asthenosphere. They also demonstrate that the upper mantle acquires its heterogeneous isotopic character through several different processes, including in situ radiogenic growth, addition of asthenospheric melts,
* Corresponding author. Fax: + 1-313-763-4690; E-mail: [email protected] 0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All rights reserved. PII: S0024-4937(99)00033-X
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dike-wall rock ionic exchange, redistribution of the lithospheric dike and vein materials by melting, and in the late stages of emplacement, assimilation of crustal materials. 9 1999 Elsevier Science B.V. All rights reserved.
Keywords: Balmuccia lherzolite massif; Dike rocks; Subcontinental lithosphere 1. Introduction Understanding the origin and evolution of continental lithosphere is a fundamental goal of solid earth geophysics, which seeks to characterize the material properties and physical state of the Earth. This goal is important because continental lithosphere records the bulk of Earth history and because a rigid lithosphere is central to plate tectonics. Although the lithosphere is defined by its physical properties, it must consist of real rocks with distinct petrologic origins and geochemical characteristics. Field-based petrologic and geochemical studies are paramount to our goal of understanding lithosphere evolution because they provide the ultimate "ground truth" for broader scale geophysical experiments that can only infer regional scale structures and average physical properties. In this contribution, we review the petrologic and geochemical characteristics of the Balmuccia lherzolite massif, a fragment of young, stabilized subcontinental lithosphere, and present new geochemical and isotopic data which constrain the origin of its peridotite and dike rock lithologies. We also present data on mafic lithologies adjacent to the massif which represent melts ponded at the crust-mantle interface subsequent to emplacement of the Balmuccia mantle diapir. The Balmuccia lherzolite massif is an alpine peridotite emplaced into granulite facies metabasites of the Ivrea-Verbano zone after the Late Paleozoic Hercynian orogeny (Shervais and Mukasa, 1991). The Balmuccia massif is characterized by fresh, unserpentinized lherzolite and dunite, and by a wide range in dike rock lithologies, including pyroxenites, websterites, and gabbronorites (Lensch, 1971; Rivalenti et al., 1975; Ernst, 1978; Shervais, 1979a; Shervais and Mukasa, 1991). The range in lithologies found within this massif is comparable with that observed in xenolith suites from alkali basalts (e.g., Wilshire and Shervais, 1975; Wilshire et al., 1988). The Balmuccia massif offers some advantages over xenolith studies, however, because structural rela-
tionships which formed in the mantle before emplacement are preserved, and crosscutting relationships between dikes of different generations and composition are readily observed. This, combined with the lack of significant low-temperature alteration throughout most of the massif make Balmuccia an ideal location to study petrologic and geochemical relations within rocks of the upper mantle. The Balmuccia massif does not represent old, Archean-type lithosphere, but rather young stabilized lithosphere, as defined by Nelson (1991). Similar lithosphere is thought to underlie extensionally stabilized orogens such as the Hercynian of Europe and the Great Basin of western North America (Menxies and Dupuy, 1991; Nelson, 1991; Shervais and Mukasa, 1991).
2. Geologic setting The Ivrea-Verbano zone represents a cross-section through the lowermost continental crust of the South Alpine plate exposed by its subsequent collision with Europe during the Alpine orogeny (Mehnert, 1975; Fountain, 1976). The Ivrea zone consists of metamorphosed supracrustal rocks (upper amphibolite to granulite facies paragneisses, calcsilicates, marbles, and charnockites), intruded by lens-shaped bodies of mafic gabbro granulites which are 8-10 km thick and > 50 km long (the so-called 'Basic Formation'). Metamorphic grade increases from SE to NW across the zone, suggesting a progression downward into the crust (Schmid and Wood, 1976; Zingg, 1980, 1983; Sills, 1984). The eastern boundary of the Ivrea-Verbano zone is the Pogallo Line, a mylonitic shear zone which separates upper amphibolite facies kinzigites of the Ivrea zone from lower amphibolite to greenschist facies gneisses and schists of the Strona-Ceneri Zone (Boriani, 1970; Hodges and Fountain, 1984). The western boundary of the Ivrea-Verbano zone is the Insubric Line, a major tectonic dislocation that separates Paleozoic
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
age rocks of the South Alpine plate from rocks of the North Alpine plate (Europe) metamorphosed during the Alpine orogeny (Gausser, 1968; Boriani and Sacchi, 1974). The Balmuccia lherzolite is one of several large, kilometer-scale peridotite massifs found within the Ivrea-Verbano zone (Ernst, 1978; Shervais, 1979a,b; Sinigoi et al., 1980, 1983; Rivalenti et al., 1981; Shervais and Mukasa, 1991). The major peridotite bodies (Finero, Balmuccia, and Baldissero) are located along the western margin of the Ivrea zone, within mafic granulites of the 'Basic Formation' (Lensch, 1971; Ernst, 1978). The Basic Formation comprises gabbro or gabbronorite granulite ( _+garnet, amphibole (amph)), clinopyroxenite, dunite, websterite, and (along its eastern margin) potassic diorites, all complexly intercalated with layers of paragneiss, marble, and calc-silicate. Petrologic and chemical studies of the Basic Formation carried out by Rivalenti and his coworkers (Rivalenti et al., 1975, 1981, 1984) suggest that it represents a single layered intrusive complex related to subduction zone magmatism along the southern margin of the South Alpine mini-plate (e.g., Hamilton, 1981). The presence of paragneiss intercalations and compositional breaks between some units of the layered series all suggest that multiple magma chambers were involved (Alberti and Longo-Salvador, 1978; Bigioggero et al., 1978; Shervais, 1979c).
3. Field relations The Balmuccia massif is an elongate lens, 4.5 km long • 0.5 km wide • 1.1 + km high, located just east of the Insubric Line, between Val Sesia and Val Mastellone (Fig. 1). The western contact of the massif is a mylonite zone several meters wide, which splays off of the Insubric line near the north end of the massif. Dikes of psuedotachylite ranging in thickness from a few centimeters to several tens of meters are common along this boundary and in the adjacent rocks. Many of these psuedotachylite dikes are characterized by columnar jointing and resemble mafic igneous dikes, but their compositions mimic their host rocks, showing that they formed in situ (Shervais, 1979c). The eastern margin of the massif is in sharp igneous contact with a series of layered
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websterites, dunites, pyroxene pegmatoids, and minor gabbronorite referred to as the Contact Series (Shervais, 1979b,c). The Contact Series intrudes the adjacent gabbro granulites and represent a thin ( < 100 m) carapace of magma which ponded at the crust-mantle boundary subsequent to, or coincident with, emplacement of the mantle peridotite at crustal levels (Shervais and Mukasa, 1991). The peridotite displays a prominent mineral foliation defined by flattened olivine and spinel grains, and by thin (1 cm) discontinuous layers of pyroxene and spinel. This foliation trends NNE in the central and southern portions of the massif, but in the northern part of the massif, and along the eastern and southeastern margins, the foliation trends NNW (Fig. 1). The NNW-trending foliation is parallel to foliations and layering in the adjacent gabbro granulites, and probably formed during emplacement of the massif into the lower crust (Shervais, 1979c). Decimeter-size pods of albite granite found within pyroxene pegmatoids of the Contact Series contain clear, euhedral zircons up to 2 mm long. One of these zircons has a concordant U - P b age of 251 ___2 Ma (Wright and Shervais, 1980). This Late Permian/Early Triassic age is somewhat younger than ages obtained from zircon in diorite near the top of the Basic Formation (285 Ma; Pin, 1986) and from monazite in paragneiss (270-275 Ma; K~Sppel, 1974; K~Sppel and Griinenfelder, 1979). This age corresponds to a post-Hercynian phase of extensional orogeny, and suggests a gap between peak metamorphism in the Ivrea zone and emplacement of the peridotite massif (Shervais and Mukasa, 1991).
4. Petrologic relations 4.1. Peridotite wall rocks
Peridotite of the Balmuccia massif consists of two main lithologies: lherzolite and dunite; harzburgite is rare. These lithologies form the pre-existing wall rock into which dikes and veins of the Cr-diopside suite, Al-augite suite, the late gabbro suite, and the hydrous vein suite were intruded. Lherzolite is by far the dominant lithology, comprising > 85% of the massif. Dunite is the next most abundant lithology
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Stronalite, Kinzigite ~
§ %
% % /
%
% % %
%
%,
% % %
% % % % % % % ,,' ,,, / / ,,, / ,,,
% % % % % / ,,4
,
Fig. 1. Geologic map of the Balmuccia massif, from Shervais (1979c).
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
and occurs throughout the massif, but is most common in the southern half. Mineral compositions in both rock types show that both lherzolite and dunite are related to dike rocks of the Cr-diopside suite. 4.1.1. Lherzolite Spinel lherzolite is the dominant rock type of the Balmuccia massif; harzburgite is rare and gradational into lherzolite (Fig. 2a). Lherzolite typically contains 60-70% olivine, 20-25% opx, and 12% clinopyroxene (cpx) by volume. The lherzolites and harzburgites are characterized by porphyroclastic textures throughout the central and southern portions of the massif, with porphyroclasts of olivine and orthopyroxene (opx) up to 1.5 cm across in a equigranularfoliate matrix (0.5-2.0 mm grain size) of olivine, pyroxene, and spinel (Shervais and Mukasa, 1991). Textures in the northern part of the massif are 'secondary protogranular' (Mercier and Nicolas, 1975), with relatively strain-free porphyroclasts, common spinel inclusions, and (in some samples) a continuous range in grain size from 0.25 mm to 2.5 cm. Along the eastern and southeastern margins of the massif the porphyroclastic texture has been overprinted by a fine-grained equigranular-foliate texture with rare relic porphyroclasts (Shervais and Mukasa, 1991). Mineral compositions in the lherzolites and harzburgites are uniformly magnesian, with olivine F089_92 (F088_89 adjacent to some Al-augite suite dikes), opx En88.5_90.5, and cpx En45Wo49. Lherzolite pyroxenes are rich in Cr, A1, and Na, but low in Ti. Spinel is variable in composition, with cr-number = [100 • Cr/(Cr + A1)] of 10-25 in normal lherzolites, and 3-12 in lherzolite adjacent to Al-augite suite pyroxenites. 4.1.2. Dunite Dunite is common in the southern and central parts of the massif, where it may comprise as much as 10% of the outcrop. Contacts between dunite and adjacent lherzolite may be sharp or gradational, and some tabular dunites with sharp contacts resemble intrusive dikes. Dunite is commonly found between or adjacent to some Cr-diopside websterites. These dunites may represent melt extraction zones related to the adjacent websterite dikes, but the volume of material in the dikes exceeds that which could be
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extracted from the wall rock locally. This implies that melt extraction probably occurred in response to magma flow through the dike conduit by a mechanism similar to the zone-refining model proposed by Quick (1981 a,b). Mineral compositions in the dunites are more refractory than in the lherzolites: olivine ranges from Fo90 to Fo91, and Cr-spinel has cr-numbers of 30-45. 4.2. Dike rocks
Dike rocks of the Balmuccia massif can be divided into four distinct suites (from oldest to youngest): the Cr-diopside suite, the Al-augite suite ("ariegites"), the late gabbro suite, and the hydrous vein suite (hornblendite). Phlogopite (phl) veins found along the eastern margin of the massif (adjacent to the Contact Series) show crustal isotopic signatures and are discussed separately below. Relative age relationships between and within these suites are based on crosscutting relations and on relative degrees of deformation in dikes that are discordant to foliation. 4.2.1. Cr-diopside suite The Cr-diopside suite comprises clinopyroxenites, websterites (4-olivine), and bronzitites (Fig. 2a). At least three generations of dikes can be demonstrated, based on crosscutting relationships: (1) thin ( < 10 cm) layers parallel to foliation; (2) thick (10-150 cm) layers subparallel to foliation (Fig. 2a), which crosscut the thin layers at low angles ( < 15~ (3) thick (10-60 cm) dikes which crosscut thick layers at moderate to high angles (Fig. 2b). Additional generations of Cr-diopside websterite can be postulated based on the occurrence of partial melting residues such as spinel streaks, 'ghost layers' of pyroxene and spinel-rich lherzolite in dunite, and Mg-rich bronzitites which are crosscut by later Crdiopside-rich veins (Shervais, 1979b). Layers which are parallel to foliation originated as dikes and were rotated into the foliation, as demonstrated by low-angle intersections between thick and thin layers and along-strike bifurcation of some thick layers (Shervais, 1979b,c; Nicolas and Jackson, 1982; Sinigoi et al., 1983). Modal mineralogy of the layers varies from nearly pure Cr-diopside to nearly pure enstatite or bronzite; olivine is a common accessory
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G
E
H Fig. 2. Field photographs of dike rocks in the Balmuccia lherzolite massif. (A) Gradational contact between dunite (the light band just to the right of the thickest dike in the photo) and lherzolite (nubbly surface coveting the fight side of the photo); both lithologies cut by foliation-parallel dikes of Cr-diopside websterite and clinopyroxenite up to 35 cm thick. (B) Discordant Cr-diopside websterite dike crosscuts older, foliation-parallel Cr-diopside websterites; top of photo to left, foliation dips ~ 45 ~ to west. (C) Al-augite suite dike of spinel-rich clinopyroxenite (gray; nearly vertical) cuts lherzolite with folded, dismembered Cr-diopside dike; note flattening of spinel parallel to foliation. (D) Zoned Al-augite dike, with margins of spinel-rich clinopyroxenite and a center of thick spinel-poor websterite. (E) Gabbronorite dike of late gabbro suite intruded parallel to foliation; top of photo to left, foliation approximately vertical. (F) Gabbro dike of late gabbro suite intruded perpendicular to foliation; note lack of deformation.
but spinel, amph, and phl are rare. Mineral compositions in the Cr-diopside suite websterites are similar
to those in the lherzolites, with olivine Fo90_91, Cr-spinels with cr-number= 5-22, and pyroxenes
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
which cover the same range in M g / F e , A1, Cr, Ti, and Na as lherzolite pyroxenes (Shervais and Mukasa, 1991).
4.2.2. Al-augite suite Dike rocks of the Al-augite suite are characterized by gray, Cr-poor, Al-rich cpx and green hercynite spinel (Shervais, 1979a,b; Sinigoi et al., 1983; Shervais and Mukasa, 1991). Kaersutitic amph is a ubiquitous accessory phase in all dikes of this suite, and plagioclase (An s0) is an accessory phase in the more differentiated members of the suite. Al-augite suite dikes crosscut dikes of the Cr-diopside suite and are always less deformed. The oldest (most deformed) members of the A1augite suite are coarse-grained (2-20 mm) spinel-rich pyroxenites that are directly comparable with A1augite suite xenoliths in alkali basalts (Fig. 2c). Al-augite suite spinel pyroxenite dikes range in thickness from 1 to 20 cm, with spinel generally concentrated near the center of the dike. They are commonly folded, with fold axes subparallel to foliation in the adjacent wall rock. Mineral compositions are relatively magnesian, with olivine Fo88_89.5 and mg-numbers in pyroxene and amph 87-90. Websterites and rare bronzitites of the Al-augite suite are more fractionated than the spinel-rich pyroxenites, and are characterized by finer grain size (1-2 mm), less abundant modal spinel, and more abundant modal opx. Plagioclase (An45_50) is a common accessory phase in the websterites, but olivine is absent. The websterites form dikes up to 1 m thick which are commonly zoned, with thin ( < 3 cm) selvages of spinel-rich pyroxenite adjacent to the wall rock and thick (10-70 cm) cores of spinel-poor websterite (Fig. 2d). Pyroxenes in the websterites and bronzitites are enriched in Fe (mg-numbers = 82-87), A1, Ti, and Na relative to the more primitive spinel-rich pyroxenites (Shervais and Mukasa, 1991). In zoned dikes, pyroxenes in the margins are more magnesian than those in the dike interiors (Fig. 3). Lherzolites adjacent to pyroxenite dikes of the Al-augite suite are enriched in FeO, TiO2, and alkalis relative to "normal" lherzolite far from any intrusions. Anhydrous silicate mineral phases reflect this enrichment with lower mg-numbers and higher minor element contents; spinel is enriched in A120 3, resulting in higher spinel mg-numbers close to the
293
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o
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~
4)
~~
i I
,
,
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Fig. 3. Electron microprobe traverse of mineral compositions in Al-augite suite dikes and in peridotite wall rock adjacent to those dikes. Samples are 2 cm in diameter drill cores taken across over a meter of outcrop. Horizontal axis is distance in centimeters from arbitrary reference point near first drill core. Vertical scales are ratios c r - n u m b e r = 1 0 0 • in spinel (top) and mgnumber = 100 • M g / [ M g + Fe] in opx (middle) and cpx (bottom). Note drops in both ratios as dikes are approached, and note drop in pyroxene mg-number within the thicker, zoned Al-augite websterite dike.
dikes as a result of the coupled MgA1-FeCr exchange (Fig. 3). Lherzolite adjacent to pyroxenite dikes may be modally enriched in amph; this amph is characterized by low mg-numbers (similar to values in the adjacent dikes) and high TiO 2 that increases with decreasing mg-numbers.
294
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
4.2.3. Late gabbro suite The late gabbro suite forms dikes 5 to 100 cm thick which are relatively undeformed, even when they crosscut the foliation at high angles (Fig. 2e,f). The general lack of deformation implies that they were emplaced late in the kinematic history of the massif, just before its emplacement into the crust. Gabbros and gabbronorites of this group vary from plagioclase-rich, with pyroxenite reaction zones 2 cm thick adjacent to the peridotite wall rock (Fig. 2f), to relatively mafic-rich with 45-55% pyroxene (Fig. 2e). Opx is ubiquitous, making these units "gabbronorites" by lithology, and kaersutitic amph is a common accessory phase. Grain size in the late gabbros varies from coarse (up to 1 cm) to fine (1-2 mm) in the more recrystallized dikes. Late gabbro dikes oriented subparallel to foliation in the lherzolite may have plagioclase-rich lenses that are flattened parallel to foliation (Fig. 2e). Most of the late gabbros are characterized by plagioclase An45_ 5o and by pyroxenes with relatively low mg-numbers compared to the Al-augite pyroxenites (75 to 80), but some dikes have mg-numbers that are quite high (88-91). In all cases, the pyroxenes have high Na, Ti, and A1, and low Cr (Shervais and Mukasa, 1991). These gabbros were formerly considered part of the A1-Augite suite of dikes (e.g., Shervais and Mukasa, 1991), but their isotopic compositions are distinct from dikes of the A1-Augite suite, requiring a different source for the parent magmas. 4.2.4. Hydrous vein suite Hornblendite veins (often referred to as "lherzites" in the older literature) are rare in the Balmuccia massif; only five have been found (Shervais and Mukasa, 1991). The hornblendite veins range in thickness from about 1 mm up to 2 cm, and consist almost entirely of kaersutite, with accessory pyroxene, hercynite spinel, and ilmenite. The veins are medium- to coarse-grained (5-25 mm) and are undeformed. The coarse grain size and lack of deformation suggest that the hornblendite veins were intruded relatively late in the kinematics history of the massif, but their age relative to the late gabbro suite of dikes is not known. Pyroxenes in the hornblendite veins have rag-numbers (87-89) similar to those in primitive Al-augite suite spinel pyroxenite dikes, but
are richer in TiO 2. The kaersutites have high mgnumbers (85-87.5), TiO 2 (3.5-4.3 wt.%), and K20 (0.7-1.0 wt.%). Lherzolite adjacent to the homblendite veins is modally enriched in amph within a few centimeters of the vein (Shervais, 1985, 1987). The modal abundance of amph and its grain size decrease rapidly with increasing distance from the veins. Textural relations and mass balance calculations show that amph within the lherzolite is being formed in part by the resorbtion of pre-existing pyroxene (Shervais, 1985, 1987; Cooke, 1992). The compositional changes show that K 20 in the melt phase percolating through the lherzolite is rapidly used up by the amph-forming reactions, such that amph formed far from the vein is lower in K 20 and TiO2, and higher in Na20 and MgO, than amph formed close to the vein (Fig. 4). The effects of this amph metasomatism do not extend more than 4 cm from a 1-cm vein. 4.3. Phlogopite veins Mica is extremely rare in the Balmuccia massif: it is found only along the SE contact area adjacent to the Contact Series, as scarce tiny flakes disseminated in lherzolite and as phl veinlets (Garuti and Sinigoi, 1978). Phl veinlets range in thickness from lmm up to 4 mm, form an irregular network in lherzolite and at least one veinlet crosscuts an Al-augite suite pyroxenite. The composition of the phl in these veinlets is similar to that reported by Garuti and Sinigoi (1978). The restriction of disseminated phl and phl veinlets to the eastern-most margin of the massif, within 2 m of the Contact Series, suggests that the mica found here is a late feature related to metasomatic exchange between the Balmuccia lherzolite and fluids emanating from the Contact Series parent magma. 4.4. Contact series Rocks of the Contact Series include dunite, harzburgite, websterite, gabbronorite, and pegmatoidal clinopyroxenite (Shervais, 1979b,c). These rocks form a thin layered intrusion (100 m thick) between the peridotite massif and gabbronorite granulites of the Lower Layered Series to the east (Fig. 1). The Contact Series has a sharp, primary igneous
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Distance from Edge of Vein (mm)
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i 0
0 10 20 30 Distance from Edge of Vein (mm)
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S.B. Mukasa, J.W. Sheruais/Lithos 48 (1999) 287-316
295
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Table 1 Whole rock analyses by XRF. Major elements in wt.% oxide, trace elements in parts per million. Fe20 ~ and FeO* are total iron as either Fe20 3 or FeO Sample no. 75B-162
75B-175B
75B-175C
75B-175A
75B-203
76B-405A
78B-707
75B-194
75B-47
76B299CW 76B-405B
78B-700
Average
Suite
Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside Cr-diopside websterite cpxite cpxite cpxite cpxite websterite websterite websterite websterite bronzitite bronzitite bronzitite WEB websterite
SiO 2 TiO 2 A120 3 Fe20 ~ FeO* MnO MgO CaO Na20 K 2O P2 05
50.2 0.17 3.67 5.56 5.00 0.11 25.75 13.53 0.10 0.02 0.02 99.13
50.9 0.16 3.08 5.96 5.36 0.14 25.09 13.19 0.42 0.02 0.00 98.96
Cr Ni Sc V Rb Sr Zr
4480 1310 52 147 nd nd 19
5900 689 41 95 nd 49 nd
Mg#
90.17
89.29
51.5 0.18 3.42 4.89 4.40 0.12 22.07 16.07 0.73 0.02 0.00 99.00 6320 691 47 111 8 57 9 89.94
50.8 0.18 3.44 5.05 4.54 0.12 23.58 15.35 0.42 0.02 0.00 98.96 6220 776 39 103 28 49 8 90.25
50.8 0.19 3.89 5.28 4.75 0.13 22.66 15.51 0.27 0.02 0.07 98.82 6250 961 58 147 21 20 11 89.48
50.5 0.20 3.75 6.36 5.72 0.13 22.17 15.98 0.01 0.02 0.07 99.19 2340 730 53 144 9 72 3 87.35
50.1 0.24 4.88 5.60 5.04 0.12 21.86 16.12 0.15 0.02 0.02 99.11 3820 1200 63 184 nd 32 nd 88.55
48.7 0.10 1.93 6.40 5.76 0.11 30.03 11.49 0.13 0.02 0.05 98.96 4090 1360 27 83 4 50 10 90.29
52.7 0.34 5.73 8.46 7.61 0.16 24.61 7.12 0.11 0.02 0.02 99.27
52.5 0.22 5.01 7.84 7.05 0.15 29.82 3.65 0.01 0.03 0.00 99.23
2210 813 31 173 nd 21 23
3280 749 22 141 nd 16 16
85.22
88.29
52.7 0.27 5.48 9.58 8.62 0.17 28.36 2.48 0.01 0.02 0.00 99.07 2720 753 17 150 4 21 5 85.43
52.3 0.44 4.70 14.82 13.34 0.24 24.84 1.58 0.01 0.03 0.03 98.99 1700 462 nd 222 nd 32 7 76.86
51.04 0.20 4.03 6.45 5.81 0.13 25.09 11.86 0.21 0.02 0.02 99.06 4330 912 41 134 7 35 9 88.57
r~ 4~
t,~ C~ I
Sampleno. 75B-44
76B-158A 769-299R
76B-300R
769-300C
76B-301C
76B-301R
76B-302C
76B-302R
76B307WR 76B307ER 76B-307C
769-522A
Suite
Al-augite Sp-Pxite
Al-augite Sp-Pxite
Al-augite websterite
Al-augite websterite
Al-augite Sp-Pxite
Al-augite websterite
Al-augite Sp-Pxite
Al-augite Sp-Pxite
Al-augite websterite
Fe2OT FeO* MnO MgO CaO Na,O K*O 52'
Cr Ni Sc
v Rb Sr Zr Mg#
Al-augite Sp-Pxite
Al-augite Sp-Pxite
Al-augite websterite
S.B. Mukasa, J.W. Sheruais /Lithos 48 (1999) 287-316
SiO, TiO,
Al-augite Sp-Pxite
Table 1 (continued) Sampleno.
76B-522B
75B-I45
75B-43
76B-351A
78B-711
76B-349A
76B333-3
78B703A3
76B333-1
76B333-2
Suite
Late gabbro gabbro
Late gabbro gabbro
Late gabbro gabbro
Late gabbro gabbro
Late gabbro gabbro
Late gabbro gabbro
Hydrous HB vein
Hydrous HB vein
Wall rock lherz
Wall rock lherz
47.1 0.76 16.66 8.53 7.68 0.14 13.43 10.55 2.14 0.05 0.05 99.41
46.5 0.85 16.54 7.29 6.56 0.12 13.68 11.45 2.55 0.06 0.03 99.07
46.5 0.93
46.1 0.87
44.9 1.01
50.2 0.40
41.8 2.97
34.5 2.79
15.30 9.48 8.53 0.15 13.82 11.04 1.86 0.04 0.01 99.13
15.10 6.79 6.1 1 0.12 16.04 11.87 1.96 0.04 0.01 98.90
15.72 9.84 8.85 0.16 13.84 11.86 2.08 0.03 0.03 99.47
21.79 1.81 1.63 0.04 6.61 13.24 4.60 0.14 0.02 98.85
9.02 7.65 6.88 0.09 26.58 7.75 2.00 0.41 0.01 98.28
10.74 7.80 7.02 0.1 1 27.58 11.37 2.13 0.59 0.00 97.61
Cr Ni Sc V Rb Sr Zr
584 386 57 174 nd 483 24
52 1 628 33 182 nd 49 1 68
824 722 42 198 nd 252 60
590 40 1 42 237 nd 310 73
14 301 22 117 16 1200 nd
3310 2080 50 27 1 nd 306 22
Mg#
75.73
78.81
82.40
73.59
87.86
87.32
io
@ SiO, TiO, *Iz03
Fe,OT FeO* MnO MgO CaO Na,O KzO 52'
44.3 0.32 3.12 9.66 8.69 0.14 39.32 1.95 0.02 0.02 0.00 99.28
40.6 0.46 3.30 9.58 8.62 0.14 40.45 3.19 0.17 0.04 0.00 98.37
ia-? -$ i
4 0,
T c 5.
e
\
S
2a
00
' I I
674 418 40 212 39 228 70 74.28
1770 2140 52 518 22 304 8 87.5 1
2090 2100 1 67 0 25 0 88.97
2080 2190 0 71 0 37 6 89.32
\O '0 L
N 3a U
2 0\
Sample no.
76B333-4
76B333-5
76B333-6
78B703A1
78B703A2
78B703A4
78B703A5
78B703A6
78B703A7
Suite
Wall rock lherz
Wall rock lherz
Wall rock lherz
Wall rock lherz
Wall rock lherz
Wall rock lherz
Wall rock lherz
Wall rock lherz
Wall rock lherz
SiO, TiO,
44.1 0.35 3.21 9.40 8.46 0.14 38.93 2.31 0.44 0.03 0.00 99.38
42.4 0.20 2.48 9.83 8.85 0.14 41.21 1.52 0.39 0.04 0.00 98.65
44.8 0.2 I 3.01 9.23 8.3 1 0.13 38.36 2.88 0.14 0.02 0.00 99.23
41.1 0.15 2.16 10.23 9.20 0.13 43.97 0.90 0.00 0.02 0.00 99.25
44.2 0.36 3.43 9.11 8.20 0.13 39.30 2.25 0.09 0.02 0.00 99.36
44.5 0.33 3.38 9.34 8.40 0.14 38.82 2.36 0.00 0.02 0.00 99.32
44.2 0.20 2.72 9.24 8.3 1 0.14 39.35 2.39 0.00 0.02 0.00 98.72
44.2 0.12 2.06 9.78 8.80 0.14 41.03 1.48 0.00 0.02 0.00 99.30
42.4 0.09 1.7 1 9.86 8.87 0.14 42.27 1.73 0.00 0.02 0.00 98.66
'4120,
FezOg FeO* MnO M&O CaO NazO KzO ' 2 O,
300
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
contact with the peridotite massif and a less distinct intrusive contact with the adjacent granulites. Northeast of the massif, the Contact Series has been repeated by faulting (Fig. 1). A layer of metapelitic granulite (stronalite) which lies just NE of the Contact Series here probably represents a septum of wall rock to the gabbronorite intrusives. Pyroxenites are the dominant lithology of the Contact Series. Both websterites (1-3 mm grain size) and clinopyroxenite pegmatoids (cpx up to 15 cm) are common. The websterites grade into gabbronorites with increasing feldspar. The pyroxenites and gabbronorites consist of pyroxene (mg-numbers 68-84), amph, plagioclase (An s0), garnet, Ti-magnetite, and ilmenite. Garnet forms as exsolution lamellae in cpx and interstitially. Peridotites in the Contact Series are dunites or harzburgites that form lens-shaped pods concordant with layering in the surrounding pyroxenites and gabbros. Equigranular-mosaic (adcumulate) textures, Fo82_87 olivine, and Cr-spinel with low mg-numbers (52-68) and low cr-numbers (10-25) characterize the peridotites. Hornblendite and amph pyroxenite veins 1-4 cm thick are common within the peridotites, as are zoned pyroxenite/gabbro dikes. The zoned dikes have pyroxenite selvages (1 to 2 cm thick) against the olivine-rich wall rock, with thick (up to 80 cm) cores of anorthositic gabbronorite.
reflects variations in the modal abundance of accumulated minerals in the dikes. Chrome concentrations co-vary with CaO, reflecting relative proportions of Cr-diopside and enstatite in the dikes, and the high concentration of Cr in cpx relative to opx. TiO 2 does not co-vary with CaO and Cr, however, despite its affinity for cpx over opx (Fig. 5). In fact, TiO 2 appears to be highest in the bronzitite dikes, reflecting in part the common occurrence of pargasite and Ti-phl in these dikes. This suggests that these bronzitite dikes crystallized from more evolved magmas than the more common cpx-rich dikes, and that they contain more residual liquid.
5.1.2. Al-augite suite Dike rocks of the Al-augite suite exhibit regular variations in major and trace element concentrations that reflect in part fractionation of the parent magmas and in part variations in the modal abundance of accumulated minerals in the dikes. Pyroxenite dikes are high in MgO, CaO, and Cr, and low in A120 3, and TiO 2 compared to the late gabbros, whereas FeO displays a similar range in both (Fig. 5). An orthopyroxenite of the Al-augite suite is rich in MgO (reflecting the high MgO content of opx). These variations are reflected in the mg-numbers of the dikes, which range from 82 to 86 in the more primitive spinel clinopyroxenites to 76 to 83 in the more evolved spinel-poor websterites.
5. Analytical results 5.1. Whole-rock chemistry Thirty-three samples of dike rock were analyzed for major and selected trace elements by X-ray fluorescence (XRF) spectrometry (Appendix A). The results are presented in Table 1. Samples from zoned Al-augite dikes have the same sample number followed by a letter indicating where in the dike the sample was taken (R = rim, WR = west rim, ER = east rim, C = core). In general the rims are spinel pyroxenites and the cores are spinel-poor websterite. Subsamples from other zoned dikes labeled A and B are noted in the descriptions.
5.1.1. Cr-diopside suite Pyroxenites and websterites of the Cr-diopside suite exhibit a range in compositions that largely
5.1.3. Late gabbro suite The late gabbro suite is characterized by gabbronorites with mg-numbers (74 to 88) that range from higher than spinel pyroxenites of the Al-augite suite (mg-numbers 82-86) to values similar to the more evolved spinel-poor websterites. These gabbros, which were intruded late in the kinematic history of the massif, crystallized at relatively lower pressures, where plagioclase saturation occurs close to the liquidus. They are higher in FeO*, TiO 2, A120 3, and alkalis than Al-augite suite pyroxenites, and lower in CaO, Cr, and Sc (Fig. 5). 5.1.4. Hydrous veins Because of their rarity and small size, we only have whole rock geochemical data for two hornblendite veins from within the massif. The veins are
301
S.B. Mukasa, J.W. Sheruais /Lithos 48 (1999) 287-316
v
V i.v.v
:; ~ /~
:: ,_,
v
...........}...................[.............
v .......
9
9
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~
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4
6000
....iZr.6i---~pxiies............
..................~, . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . -.........2~ ' " i ,. ....!-......-~r ........ ~................... ! ...............
~
., ....................
9
1000
-iaieeabbro
Fig. 5. Mg-number variation diagrams for dike rocks of the Balmuccia massif and for some lherzolite wall rocks. Symbols: ( O ) Cr-diopside suite; ( O ) Al-augite suite; ( U ) late gabbro suite; (4,) hornblendites" ( + ) lherzolite and dunite.
characterized by high mg-numbers
( 8 7 ) a n d T i O 2,
and by lower CaO, AI203, and Cr than correspond-
i n g d i k e s o f the A l - a u g i t e suite (Fig. 5). B u l k r o c k analyses
o f serial
slabs
of wall rock
adjacent
to
1N
8L
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~ 6.o 2..
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303
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
Table 2 Clinopyroxene and amphibole trace element data by SIMS for three of the rock suites in the Balmiccia massif. Abbreviations for the material analyzed are as follows: amph, amphibole; cpx, clinopyroxene Sample and material analyzed
Rock type
La
Ce
Nd
Sr
Sm
Zr
Ti
Eu
Dy
Y
Er
Yb
V
Cr
Cr-diopside lherzolite suite 90B-722-1 cpx (a) Lherzolite 90B-722-1 cpx (b)
0.14 0.09
0.48 0.37
1.47 1.24
6.9 7.9
1.02 0.98
7.2 5.4
1772 1684
0.42 0.41
2.41 2.30
13.7 12.8
1.55 1.48
1.85 281.1 1 . 6 1 290.5
Spinel pyroxenite suite 75B-158 cpx (a) Pyroxenite 75B-158 cpx (b) 75B-158 cpx (c) 76B-307R cpx Pyroxenite 90B-719 cpx (a) Pyroxenite 90B-719 cpx (b)
0.86 1.43 1.31 0.80 0.65 0.67
4.62 7.15 6.69 3.17 2.75 2.70
7.61 8.85 8.67 3.67 3.54 3.81
36.7 49.0 47.1 40.9 38.4 39.7
3.55 4.33 3.95 1.90 1.84 1.96
33.1 52.3 35.3 22.8 14.3 12.2
6694 7857 6804 3738 3430 3384
1.43 1.59 1.48 0.74 0.68 0.72
4.69 5.27 4.92 2.76 2.81 2.87
17.6 24.0 19.2 17.0 16.9 16.5
2.63 2.78 2.78 1.80 1.84 1.54
2.69 3.02 2.87 1.90 1.76 1.68
486.2 521.4 477.1 472.7 478.6 491.7
421.8 189.6 181.3 232.3 148.8 175.3
Gabbronorite 3.21 2.35 Gabbronorite 1.67
14.67 11.56 9.02
16.10 12.59 11.90
596.3 81.6 81.5
6.44 5.23 5.30
102.7 118.5 102.4
32506 8045 10111
3.26 2.46 2.05
9.42 6.47 7.79
58.9 34.0 40.7
5.75 3.37 4.31
6.50 3.63 4.58
806.1 329.9 437.2
982.0 521.7 773.7
Late gabbro suite 75B-142 amph 75B-142 cpx 76B-522B cpx
hornblendite veins show that the lherzolite wall rock is enriched in A1203, CaO, TiO 2, Na20, and K20
5632 5245
relative to lherzolite far from the veins (Fig. 6). The overall effect on the major oxides does not seem to
AI-augite
Suite
v/~...vaa42~
E >
'___r," F.~-P T~., ." % ' -
E
._ !_
10 ('3
E 03 t~
-
-
// //
Fig. 7. Trace element patterns for cpx and amph normalized to the PRIMA values of Sun and McDonough (1989). The diagram includes patterns for cpx from one sample of Cr-diopside suite lherzolite, two samples of Al-augite suite pyroxenites, and three samples of the late gabbro suite. It also includes one pattern for amph from a late gabbro suite feldspathic websterite. Most of the samples have been analyzed in duplicates to assess reproducibility. The Cr-diopside websterite compositional range shown with the stippled pattern is from Rivalenti et al. (1995). See text for discussion.
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persist for more than 4 cm away from these veins, which are less than 2 cm thick. 5.2. Trace element concentrations in cpx and amph
Concentrations of the rare earth elements (REE) La, Ce, Nd, Sm, Eu, Dy, Er, and Yb, and the trace
elements Sr, Zr, Y, Ti, V and Cr have been determined by secondary ionization mass spectrometry (SIMS) on cpx and amph and normalized to the primitive mantle (PRIMA) values of Sun and McDonough (1989). The data are listed in Table 2 and are presented graphically in Fig. 7. The Cr-diopside
N O.lO
E
"r-
E (13
E
_
E
Fig. 8. Sets of diagrams with bulk-rock REE and trace element abundance patterns determined by INAA for two hornblendite veins (76B-333 and 78B-703A) and serial slabs of the wall rock around them. The legends for diagrams (b) and (d) also apply to diagrams (a) and (c), respectively. The numerical values marking each symbol are distances in centimeters on either side of each vein. See text for discussion.
S.B. Mukasa, J.W. Shervais / Lithos 48 (1999) 287-316
suite sample analyzed in duplicates as a measure of reproducibility (90B-722-1) is a typical lherzolite, far from any of the dikes in the massif. Its cpx has strong light REE depletions (La at ~ 0.1 to 0.2 times PRIMA) and flat heavy REE at ~ 3 times PRIMA. Moreover, it has the lowest Sr, Zr and Ti concentrations measured, but has more pronounced positive anomalies of Y and V compared to the other samples. The stippled fields on the diagram in Fig. 4, based on SIMS cpx data by Rivalenti et al. (1995), show that websterite dikes of the same Cr-diopside suite are generally more enriched in the light REE than the host lherzolite (assuming that we analyzed a representative sample of the host rock). These dikes also have slightly lower heavy REE, similar Zr and Ti, and higher Cr and Sr compared to the host lherzolite. Two samples of the Al-augite suite (75B-158 and 90B-719) have been analyzed in triplicate and duplicate, respectively, to document reproducibility, and one other sample from this group (76B-307R) has been analyzed just once (Fig. 7). Cpx from the three samples displays light REE concentrations that are either slightly higher than or are comparable to those in cpx from the Cr-diopside suite dikes. However, they have higher heavy REE concentrations overall compared to the cpx from the Cr-diopside suite websterites, but overlap with the cpx from the host lherzolite sample. Also, cpx from all three samples
305
of the Al-augite suite have Sr, Zr, Y, Ti, V and Cr concentrations that are higher than those in cpx from all the rocks of the Cr-diopside suite. Two samples of the late gabbro suite have been analyzed both amph and cpx from sample 75B142 and cpx from sample 76B-522B (Fig. 7). Cpx from this suite has the highest overall concentrations of REE, and additionally exhibits the only positive Eu anomaly observed for all rock suites. Sr, Zr, Y, and Ti in the late gabbro suite cpx are also the highest of all those measured. V and Cr in cpx are intermediate between the low and high values for cpx in the Cr-diopside suite lherzolite and Al-augite suite dikes. Amph from gabbronorite sample 75B-142 has the highest overall concentrations for all of the elements except Zr and Cr. 5.3. Trace elements in bulk hornblendite veins and adjacent serialized host lherzolite domains
Two hornblendite veins of nearly pure kaersutite (76B-333 and 78B-703) and serialized adjacent host lherzolite domains have been analyzed for bulk rock REE and Ba, Th, U, Ta, Hf, Zn, Sc, Cr, Co, and Ni concentrations to assess the character and degree of ionic exchange between the host rock and the fluid phase or magma that formed the veins (Fig. 8 and Table 3). Both veins have convex though not identical REE patterns with the middle REE reaching 5
Table 3 Trace element data (by INAA) for two hornblendite veins and their serialized host lherzolite slabs. Concentrations are in parts per million Sample
From vein (cm)
76B-333-1 76B-333-2 76B-333-3 76B-333-4 76B-333-5 76B-333-6 76B-333-7 78B-703A-1 78B-703A-2 78B-703A-3 78B-703A-4 78B-703A-5 78B-703A-6 78B-703A-7
- 2.1 - 1.0 Hblvein +1.25 + 2.75 +4.25 > 4.25 -3.1 - 1.5 Hbl vein + 1.5 +3.0 +4.5 +6.1
Ba
Th
U
Ta
15 0.1 0.1 18
100
15
0.14 0.02
La
Ce
0.16 0.10 0.47 0.08 0.06 0.12 0.21 0.08 0.06 0.41 0.09 0.09 0.06 0.07
0.68 0.76 2.40 0.24
1.10 0.81
Nd
5
Hf
Sm
Eu
Tb
Yb
Lu
Zn
Sc
Cr
Co
Ni
0.21 0.22 0.45 0.19 0.17 0.24 0.32 0.08 0.21 0.34
0.24 0.35 1.88 0.26 0.15 0.31 0.30 0.08 0.25 1.79 0.22 0.18 0.10 0.09
0.08 0.13 0.78 0.10 0.06 0.11 0.12 0.03 0.08 0.73 0.08 0.07 0.04 0.03
0.06 0.08 0.47 0.05 0.07 0.08 0.10 0.02
0.31 0.37 1.64 0.33 0.24 0.34 0.47 0.06 0.21 0.84 0.17 0.21 0.14 0.21
0.05 0.05 0.22 0.05 0.03 0.06 0.07 0.01 0.04 0.14 0.04 0.03 0.02 0.03
60 53 43 54 45 43 53 61 61 84 51 50 48 43
10.8 12.7 31.5 11.4 9.5 13.7 16.4 6.3 13.3 34.4 12.7 13.9 10.5 10.8
2122 2221 3376 2601 2183 2340 2462 3012 2362 1908 2040 2552 2385 2232
113 106.2 88.3 112.1 115.9 108.6 102 132 110.9 88.7 109.4 107.2 115.6 116
2041 1986 2012 2043 2141 1966 1877 2552 2124 1970 2067 1996 2132 2202
0.16 0.17
0.44 0.05
306
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times PRIMA and the light REE considerably less abundant than the heavy REE. In addition, they have on average at least five times the concentration for every REE analyzed (except La and Ce) compared to the host lherzolite slabs. This difference in concentrations is also generally true for the rest of the highly incompatible trace elements (e.g., Ba and Th), but not for the most compatible elements (e.g., Cr, Co and Ni). Most striking of all for sample 76B-333 is that slabs of host lherzolite closest to the hornblendite vein do not have the highest trace element concentrations. Rather slabs at 4.25 and > 4.25 cm from the contact have the higher values compared to slabs at 1, 2.1 and 2.75 cm away from the contact. Moreover, the trace element distribution is not symmetrical, in the sense that slabs that are equal distant from but on opposite sides of the vein do not have the same trace element concentrations.
In contrast, for sample 78B-703A, slabs that are closest on either side of the hornblendite vein have the highest trace element concentrations. Asymmetry in trace element distributions is observed for this sample as well in the slabs at about 3 cm on either side of the vein. Though not every element was analyzed in all of the samples, the limited available data indicate that Ba and Th are enriched in both the hornblendite veins and adjacent host lherzolite. While there are differences between slabs, overall most have not deviated much in pattern and concentration from the "average lherzolite from Balmuccia" values in (Hartmann and Wedepohl, 1993).
5.4. Isotopic compositions Mineral separates from 16 samples have been analyzed for the isotopic compositions of Sr and Nd,
Table 4 Rb-Sr, S m - N d and U - P b isotopic and concentration data. Analytical errors for 878r/86Sr and 143Nd/144Nd are based on the 20- in-run statistics. Errors for the Pb isotopic ratios are 0.1%, based on replicate analyses of NIST standard SRM-981. Abbreviations for the material analyzed are as follows: amph, amphibole; cpx, clinopyroxene. The e values were calculated using the m3Nd/144Nd value for chondritic uniform reservoir (CHUR) at 250 Ma of 0.512316 Sample and material analyzed
Rock type
Rb (ppm)
Sr (ppm)
87Rb/868r
( 87Sr/86Sr)t250
Sm (ppm)
Nd (ppm)
147Sm/ 144Nd
Cr-diopside lherzolite and websterite suite 90B-715 cpx Websterite 0.001 90B-716 cpx Websterite 0.002 90B-718 cpx Lherzolite 0.003 90B-721 cpx Websterite 0.005 90B-722-1 cpx Lherzolite 90B-723-4 cpx Lherzolite
25.9 36.2 13.6 23.6 5.7 5.2
0.00013 0.00013 0.00055 0.00058
0.70334 _+ 1 0.70374 _+ 1 0.70349 _+ 1 0.70324_ 1 0.70345 • 1 0.70303 _+ 6
0.1 1.1 1.3 0.7 0.9 0.8
4.1 2.7 1.7 1.1 1.1
0.15800 0.30594 0.24614 0.46044 0.47080
Spinel pyroxenite suite 75B-158 cpx Pyroxenite 76B-300C cpx Websterite 76B-300R cpx Pyroxenite 76B-302C cpx Websterite 76B-302R cpx Pyroxenite 76B-307C cpx Websterite 76B-307R cpx Pyroxenite 90B-719 cpx Pyroxenite
0.133 0.042 0.051 0.024 0.041 0.031 0.054 0.001
34.5 26.5 28.5 25.6 28.9 29.9 29.4 16.8
0.0028 0.00098 0.00114 0.00045 0.00091 0.00053 0.00122 0.00025
0.70270 0.70320 0.70305 0.70301 0.70324 0.70302 0.70295 0.70311
+_ 1 _+ 1 + 1 _+ 1 _+ 1 _+ 2 _+ 1 _+ 2
3.3 2.1 0.9 1.1 1.5 1.8 1.6 1.1
8.0 4.9 2.0 2.5 3.7 4.3 3.7 2.3
0.25167 0.26064 0.26715 0.26557 0.25396 0.25320 0.26223 0.29095
Late gabbro suite 75B-142 amph 76B-522B cpx
Gabbronorite 1.489 Gabbronorite 0.042
282 75.4
0.00925 0.00031
0.70214 +_ 1 0.70216 _+ 1
4.9 4.1
13.1 10.2
0.22556 0.24578
Hornblendite suite 90B-725 amph
Hornblendite
348
0.70289 + 1
4.8
15.8
0.18316
307
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and most for the concentrations of Rb, Sr, Sm, and Nd as well (Table 4 and Fig. 9). Thirteen of the samples have also been analyzed for their Pb isotopic compositions, and when possible for their U and Pb concentrations. Details for the analytical procedures are provided in Appendix A. It is assumed in presenting these results that appreciable diffusive exchange between minerals in the lherzolite and dikes was possible until the massif cooled through the blocking temperature for zircon of ~ 900~ (Mezger, 1990) at 250 Ma (Wright and Shervais, 1980). Hence, ~~ values and " i n i t i a l " Sr isotopic ratios have been calculated for 250 Ma. 5.4.1. N d and Sr isotopic compositions The new Nd and Sr isotopic data represent five samples from the Cr-diopside suite, eight from the Al-augite suite, two from the late gabbro suite, and one from the hydrous vein suite. These are compared in Fig. 9 to the mid-ocean ridge basalt ( M O R B ) field
(143Nd/ 144Nd)t250
(gNd)t250
U (ppm)
0.51255 + 2 0.51264 __+2 0.51260 __+2 0.51307 __+2 0.51276 __+2
+ 4.6 +6.4 + 5.6
0.51260 • 0.51264 • 0.51267 • 0.51266 • 0.51262 • 0.51262 + 0.51265 • 0.51259 •
2 2 2 1 1 1 1 1
+ 5.6 +6.3 + 7.0 + 6.8 + 6.0 + 5.9 + 6.5 + 5.4
0.005
0.51284 __+1 0.51283 __+2
+ 10.2 + 10.0
0.51270 __+2
+ 7.6
0.01 0.004 0.01
(Zindler and Hart, 1986), local granulite and kinzigite in the crustal basement (Pin and Sills, 1986; Voshage et al., 1988; Lu et al., 1997), and our earlier determinations (Shervais and Mukasa, 1991) on six Cr-diopside suite websterite dikes, two late-stage gabbronorite dikes, two hornblendite veins in lherzolite, one phl vein in lherzolite, and two Contact Series rocks from outside the massif (a pyroxene pegmatoid and a hornblendite vein in cumulate dunite). The five new Cr-diopside samples are remarkably similar in their Nd and Sr isotopic compositions to our earlier six determinations for this suite, and together define a cluster that fall within the field for ocean island basalts (OIB) at the time of emplacement of the massif at 250 Ma (Fig. 9). This range exceeds the analytical uncertainties for each point and is clearly unlike M O R B . However, the cluster would be even smaller were it not for samples 75B-194 and 90B-716 which have the lowest end values. Sample 75B-194 is a 3-cm
Pb (ppm)
206Pb/204 Pb
207Pb/204 Pb
208Pb/204 Pb
0.30
18.512 18.597
15.660 15.654
38.396 38.549
0.30 0.13 0.13
0.9 5.5
18.422 18.564 18.534
15.592 15.623 15.572
38.240 38.375 38.276
2.2
0.004 0.003 0.004 0.005 0.005 0.009
0.1 0.3 0.4 0.3 0.2 0.4 0.2 0.3
0.6 0.7 1.0 0.7 1.5 1.7
18.548 18.338 18.345 18.363 18.367 18.260 18.431 18.357
15.594 15.618 15.609 15.612 15.595 15.594 15.598 15.612
38.557 38.150 38.224 38.247 38.215 38.046 38.134 38.293
0.006 0.007
0.25 0.05
1.4 9.2
18.145 18.308
15.586 15.564
37.951 37.952
18.517
15.592
38.306
+ 8.6
0.24
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15
10
0
Fig. 9. Sr-Nd: (a) ENd VS. initial 87Sr/86Sr diagram for cpx, amph, and phi mineral separates from the various dike suites of the Balmuccia massif. Assuming that diffusive exchange between minerals was possible until emplacement of the pefidotite body into the lower crust, the isotopic compositions have been corrected for decay using an age of 250 Ma (Wright and Shervais, 1980). Data for the Contact Series rocks and 10 of the other 27 points plotted are from Shervais and Mukasa (1991). Granulite and kinzigite data, which overlap the range plotted (here shown with an arrow), are from Pin and Sills (1986), Voshage et al. (1988), and Lu et al. (1997). The MORB field is from Zindler and Hart (1986) and references therein.
single crystal from an unrecrystallized websterite dike with 87Sr/86Sr = 0.70351 and 143Nd/144Nd = 0.51242 (eNd = +2.2) while 90B-716 comes from the less deformed group of the Cr-diopside suite websterites and has 87Sr/86Sr = 0.70374 and 143Nd/144Nd -- 0.51253 (eNd = + 4.2). These values may reflect the primary compositions of at least some of the Cr-diopside websterite dikes before recrystallization and re-equilibration with the host lherzolites ( 8 7 S r / 8 6 S r = 0.70339-0.7055, eNa = + 6.5 to + 7.2, determined on whole-rock powders; Voshage et al., 1988). All of the cpx separates from the Al-augite suite, except sample 75B-158, overlap completely with the field for the volumetrically dominant Cr-diopside suite. This suggests either that melting of lithospheric materials similar to the Cr-diopside suite generated the Al-augite suite magmas or that these dikes may have had a different source area but have largely equilibrated with the Cr-diopside suite via subsolidus diffusion.
The two new analyses of cpx from the late gabbro dike suite (75B-142 and 76B-522B) are strongly depleted in the heavy isotopes of Sr and Nd relative to the other samples studied here, with 87Sr/S6Sr = 0.70217-0.70218 a n d 143Nd/144 Nd = 0.512800.51281 (eNd = + 9 . 4 - - + 9.6)(Fig. 9 and Table 4), which is indistinguishable from the earlier two determinations for this suite by Shervais and Mukasa (1991). These isotopic compositions are similar to MORB and are distinct from the OIB-like compositions that characterize other lithologies of the massif. One new kaersutite from hornblendite suite sample 90B-725 has been analyzed for comparison with the two earlier determinations by Shervais and Mukasa (1991). Two of the three samples are very similar in their Nd and Sr isotopic compositions to the Cr-diopside suite and the majority of the samples from the Al-augite suite. The third one has a MORB-like Sr isotopic composition though a somewhat lower Nd value (Fig. 9). We have included on the diagram in Fig. 9 the field for the isotopically
309
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37
'/
I
,
I
,
I
,
Fig. 10. (a) 2~176 vs. 2~176 and (b) 2~176 vs. 2~176 variation diagrams for cpx and amph mineral separates from the dike suites of the Balmuccia massif. The symbols used are the same as in Fig. 9. Note that there are still no Pb data for the rocks of the Contact Series. The present-day MORB field and Northern Hemisphere reference line (NHRL) from Hart (1984) and Zindler and Hart (1986) are included for comparison.
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enriched pegmatoidal pyroxenite, hornblendite and glimmerite ( > 90% phl) first reported by Shervais and Mukasa (1991), now all recognized to be associated with the intrusive Contact Series along the southeastern margin of the massif.
5.4.2. Pb isotopic compositions The Pb isotopic data are presented in Table 4 and diagrams in Fig. 10. Their acquisition from Balmuccia mineral separates has been a challenge because of the exceedingly low concentrations of Pb ( ~ 50400 ppb). For most samples, however, the blank was < 10% of the total Pb analyzed. One measure of the robustness of the Pb data is the good reproducibility obtained on cpx separates from the margins and interiors of the compositionally zoned Al-augite suite dikes (spinel pyroxenite at the margins and websterite in the interiors for samples 76B-300, 76B-302, and 76B-307). U concentrations in the cpx are < 12 ppb which in the average sample sizes used for isotope dilution ( ~ 6 mg) yielded ~ 70 pg of U or less. This value not being much larger than the total U blanks of 10-40 pg (with most around 20 pg), we have decided not to make any decay corrections on the Pb ratios, except for one demonstration data point which shows the effect to be small. This data point is shown as a black square with a cross which with the decay correction shifts to the position of the gray square with a cross on the 2~176 vs. 2~176 diagram (Fig. 10a). The effect on the 2~176 vs. 2~176 diagram (Fig. 10b) seems to be more substantial. However, the T h / U value used in the decay correction was assumed from generalizations about mantle compositions. Fig. 10 shows the Pb isotopic compositions to be more diverse in the Cr-diopside suite than in either the Al-augite suite or the late gabbro suite. Within the Cr-diopside suite, the websterite dikes are more heterogeneous than the host lherzolite samples and include samples with the most radiogenic Pb compositions. Similar to the relationships on the Nd-Sr diagram in Fig. 9, the field for the Al-augite suite overlaps almost completely with the Cr-diopside field, but is itself much smaller and toward the less radiogenic end of the cluster. The least radiogenic values of all belong to an amph from sample 75B-142 and cpx from sample 76B-522B, two gabbronorites of the late gabbro suite (Table 4 and Fig. 10). This
character is consistent with the MORB-like Nd and Sr isotopic signatures the samples exhibit in Fig. 9. Note that all of the samples fall above the present-day MORB field on the 2~176 vs. 2~176 diagram (Fig. 10a) but that they fall within it on the 2~176 vs. 2~176 diagram (Fig. 10b). The significance of this might be a time-integrated record of high U / T h in the lithospheric mantle represented by the Balmuccia peridotites and in the sublithospheric source materials for the dikes and veins.
6. Discussion
6.1. Relationship between tectonism and deformation The Balmuccia massif represents a small fragment of subcontinental lithospheric mantle which was emplaced into lower continental crust during an episode of Late Permian extensional tectonics (Shervais and Mukasa, 1991). Before its emplacement at crustal levels, this lithospheric mantle underwent a long history of partial melting, magmatic intrusion, and plastic flow deformation. The evidence for these events is preserved as dikes of the four main intrusive series described here: the Cr-diopside dike suite, the Al-augite dike suite, the late gabbro dike suite, and the hydrous vein suite (hornblendites). These dikes record the evolution of the subcontinental lithospheric mantle of southern Europe before the Late Paleozoic Hercynian orogeny, and provide us with insights into the processes involved in the chemical fractionation of the Earth's mantle.
6.2. Dike suites in the subcontinental lithospheric mantle 6.2.1. Cr-diopside suite Field and chemical evidence shows that websterites of the Cr-diopside suite represent a series of magmatic events that affected the upper mantle over an extended period of time. Chemical variations within dikes of the Cr-diopside suite reflect crystal accumulation from a magnesian parent magma. Pyroxenite and websterite compositions can be effectively modeled as mixtures of Cr-diopside and enstatite, with only traces of residual liquid (now
S.B. Mukasa, J.W. Shervais /Lithos 48 (1999) 287-316
represented modally by interstitial amph and phl). The predominance of Mg-rich mineral compositions in these dikes implies that the parent magmas underwent limited evolution by crystal fractionation within the mantle. However, these dikes may have been affected by melt extraction events after their formation. Many Cr-diopside suite dikes are clearly intrusive into their surrounding rocks. In particular, some younger Cr-diopside suite dikes crosscut older, concordant dikes at high angles and offset them dilationally (e.g., Fig. 2b). The evidence for at least three generations of Cr-diopside suite dikes, and the occurrence of older Cr-diopside suite layers that have been affected by later melting events, shows that this suite does not represent a single magmatic episode. Isotopically, websterites of the Cr-diopside suite resemble OIB. Similar isotopic compositions were found in whole-rock samples of lherzolite by Voshage et al. (1988). The mantle source region of the Balmuccia massif formed part of the subcontinental lithospheric mantle before its emplacement, and it was underlain by MORB-type asthenosphere (shown by the intrusion of MORB dikes late in its history). Evidence from xenoliths (Frey and Green, 1974; Frey and Prinz, 1978; Downes, 1987; Zindler and Jagoutz, 1988; Menzies, 1989), alpine massifs (Loubet and Allegre, 1982; Menzies and Halliday, 1988; Fabries et al., 1991; Menxies and Dupuy, 1991; Reisberg et al., 1991), mafic lavas (Weaver and Tarney, 1981; Fitton et al., 1988; Leat et al., 1988; Hart et al., 1989), and geophysical constraints (Jordan, 1978, 1988) suggests that many sections of subcontinental lithospheric mantle formed by the reenrichment of depleted, "infertile" peridotie similar to MORB-source asthenosphere. This implies that subcontinental lithospheric mantle is chemically and isotopically zoned either vertically or laterally (e.g., Menzies, 1989, 1990; Menxies and Dupuy, 1991).
6.2.2. Al-augite suite We suggest that the Al-augite suite formed by polybaric fractionation of an alkaline, aluminous parent magma yielding the spinel pyroxenites and websterites that crosscut the older Cr-diopside suite dikes. Formation of the Al-augite dike series by within-dike crystal fractionation is demonstrated by mineral chemical and whole-rock chemical trends of FeO*,
311
TiO 2, A120 3, and alkali enrichment, and by field relations which show within-dike zonations from spinel pyroxenite to websterite (Shervais, 1979b; Sinigoi et al., 1983). In zoned dikes, more primitive mineral and whole-rock compositions are found in the dike margins (adjacent to the wall rock) whereas the more evolved mineral and whole rock compositions are found in the cores (Fig. 3). These relationships imply that fractionation proceeded by nucleation of crystals on the dike walls, and by reaction between the evolving magma and its magnesian wall rock. Isotopically, rocks of the Al-augite dike series have OIB-like compositions that overlap dikes of the Cr-diopside suite. This implies that, despite the differences between these two suites in parent magma composition and evolution, they were derived from an isotopically similar source region in the lower subcontinental lithospheric mantle.
6.2.3. Late gabbro suite The late gabbros crystallized at lower pressures than the Al-augite suite pyroxenites, where plagioclase saturation occurs near the liquidus. They commonly have reacted margins of pyroxenite that separate the feldspar-rich core from the olivine-rich wall rocks. Mineral chemical and whole-rock chemical trends suggest that the parent magma of the late gabbro dikes was lower in TiO 2 and higher in A120 3 and Na20 than the older Al-augite dike series. In addition, the late gabbro dikes have isotopic composition similar to MORB, and must have been derived from the convecting asthenosphere below the lithospheric source of the lherzolite massif. Thus, emplacement of these dikes is probably related to extensional thinning of the lithosphere and the concomitant rise of asthenosphere mantle during extension (Shervais, 1979a; Shervais and Mukasa, 1991). Cpx in the late gabbro suite is also predominantly Al-augite, which might suggest a genetic link between this suite and the spinel-rich pyroxenites of the Al-augite suite (sensu stricto). The MORB-like isotopic compositions of cpx from the late gabbros, however, show that these rocks and Al-augite suite pyroxenite and websterites were derived from at least two isotopically distinct source regions within the mantle, and do not represent differentiation of a single consanguineous magma suite.
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6.2.4. Hydrous vein suite Hornblendites of the hydrous vein suite are enigmatic. Amphiboles in the veins are compositionally distinct from accessory amph in the older Al-augite suite dikes and thus cannot represent residual fluids filter-pressed from pyroxenites, as has been proposed for hornblendite veins in the Lherz massif (Wilshire et al., 1980). Chemically similar accessory amph are found in the late gabbro dikes; however, the vein amph have OIB-like isotopic signatures similar to Cr-diopside websterites and the older Al-augite suite dikes, and distinct from the MORB-type signatures of the younger gabbro dikes. These data suggest that the hornblendite veins represent a separate intrusion of water-rich magma, derived by small fractions of partial melting of the lower subcontinental lithospheric mantle (Shervais and Mukasa, 1991). Ionic exchange between the hydrous vein melts and the lherzolite wall rocks occurred over distances of just a few centimeters. While the asymmetrical distribution of trace elements in the serialized lherzolite domains around the hornblendite veins might suggest some chromatographic effects (e.g., Navon and Stopler, 1987), the evidence is more compelling in the Balmuccia massif for two other possibilities. One is that the trace element heterogeneity could be accounted for by the decimeter-scale mineralogical variations in the host rocks. The other is that dikes and veins remobilized by melting, and there is ample evidence of this, have left ghost domains in the lherzolite with elevated trace element concentrations.
tism, with the addition of abundant kaersutite immediately adjacent to the vein, and progressively less amph further away. Interstitial amph in lherzolite near the vein is rich in K20 and has a high K20/Na20 ratio; K20 concentration and K20 / Na20 drop rapidly at greater distances from the vein (Fig. 4). Similar variations are seen in whole rock compositions (Fig. 6). Both situations apparently involve the percolation of magma into the wall rock from the intrusions and reaction between this magma and the pre-existing phases. In both cases, the extent of metasomatism does not extend more than a few decimeters into the lherzolite wall rock. This distance is controlled in part by the volume of magma or metasomatic fluid available: metasomatized zones are thinnest next to cm-scale hornblendite veins, and thicker next to decimeter scale dikes. When this magma penetrates the wall rock, some components (e.g., K20) are quickly consumed by reactions between the magma and pre-existing phases, leaving a residual melt which is depleted in these components relative to the parent magma. These data show that pervasive metasomatism of lithospheric mantle is not possible without large volumes of magma or metasomatic fluids. It is important to remember, however, that this fluid is added to the lithosphere most effectively as dikes and veins which alter the bulk composition of the lithosphere (on the scale of partial melting) even if metasomatism of the lherzolite wall rock is limited. 6.4. Crust-mantle interactions during emplacement
6.3. Metasomatic effects of dike and vein intrusion on wall rock
Lherzolites adjacent to Al-augite suite dikes and hydrous veins exhibit systematic changes in their whole-rock chemistry, mineral chemistry, and modal mineralogy, which reflect metasomatic exchange between the lherzolite and the intrusive magmas. These changes differ in their nature and extent depending on the size and composition of the intruding magma. Lherzolite adjacent to Al-augite suite dikes is enriched in A1, Fe, and Ti, as shown by lower ragnumbers in pyroxenes adjacent to Al-augite dikes, and by spinels with lower Cr203 and higher A1203 near the dikes (Fig. 3). Lherzolite adjacent to hornblendite veins undergoes pervasive modal metasoma-
The last magmas to accompany the massif during its rise to crustal levels ponded at the crust-mantle interface to form the layered Contact Series. These melts crystallized at lower pressures than the older dike rocks within the massif, and experienced more extensive fractional crystallization. During crystallization, the Contact Series magma assimilated portions of the adjacent gabbro granulites, and absorbed fluids containing an isotopically enriched component. These interactions with crustal material resulted in the addition of a crustal isotopic signature to the Contact Series that obscured their original magmatic affinity. Fluids from the Contact Series penetrated the adjacent lherzolite body (driven by chemical potential gradients between the lherzolite and the
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magma) to form phl veins and disseminated phl; other fluids penetrated cumulate dunites within the Contact Series and Lower Layered Series to form hornblendite veins. All of these hydrous vein minerals have crustal isotopic signatures, in contrast to the hornblendite veins within the massif.
7. Conclusions The Balmuccia lherzolite massif preserves clearly the evolutionary development of subcontinental lithospheric mantle. The pre-emplacement history of this massif involved repeated episodes of partial melting and magma intrusion, accompanied by continuous plastic deformation. Judging from the intense degree of deformation exhibited by the oldest dikes, it appears that many of these dikes may have been injected into the peridotite before the massif became stabilized at the base of the subcontinental lithospheric mantle. The occurrence of minerals with OIB-like Nd and Sr isotopic compositions shows that melts with these geochemical characteristics are not always direct products of plume magmatism originating at deeper levels in the mantle. These results suggest that such melts could be generated in the subcontinental mantle lithosphere. Though not constrained by our results, it is likely that the subcontinental lithospheric mantle acquired the isotopic signature from the diapiric rise of OIB-asthenosphere plumes. Later emplacement of this subcontinental mantle lithosphere at crustal levels involves extensional orogenesis, accompanied by renewed melting and magma intrusion. The provenance of these melts changes with time, from lithosphere derived to asthenosphere derived, in response to thinning of the lithosphere and uplift of the underlying asthenosphere. The generation of basaltic melts from mantle source regions that have undergone similar complex histories clearly involves a variety of processes whose effects will be difficult to discern. The remelting of older dike rocks in particular offers the possibility of tapping chemically and isotopically distinct source regions that may coexist on a scale of meters. If these dikes/veins include hydrous phases rich in light rare earth elements (LREE) and Rb/Sr, later melting events can create a cryptic enrichment in the
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heavy isotopes of Sr and Nd which can no longer be correlated with the older modal metasomatic event. The complexities observed over short distances within the Balmuccia massif also suggest caution in the interpretation of xenolith chemical and petrologic data, as we cannot observe the structural context where they originated.
8. Uncited reference Wernicke, 1985
Acknowledgements This manuscript benefited greatly from reviews by Tanya Furman and Bill McDonough, and from discussions with our colleagues, H.G. Wilshire, J.E. Nielsen and A.V. Andronikov. We also wish to thank A. Koh and S.R. Zeff for assistance with mineral separations, mass spectrometry and manuscript preparation. This work was supported by the National Science Foundation grants to S.B.M. and J.W.S.
Appendix A. Analytical methods A. 1. Sample preparations Whole-rock powders were prepared from samples free of any visible surface weathering using standard procedures of jaw-crushing pre-cleaned rock chips. Mineral separates were also prepared from unweathered samples using nylon sieves for sizing, a magnetic separator, and hand picking under a binocular microscope. Prior to dissolution for the isotopic analyses, the mineral separates were acid washed in warm, distilled 2.5 N HC1 for 15 min, and warm distilled 5% HF also for 15 min, with an H 20 rinse after each of these steps. A.2. XRF and instrumental neutron activation analysis (INAA) XRF analyses were performed with a Philips PW1400 spectrometer at the University of South Carolina. Samples were prepared as fluxed glass disks using a Li tetraborate flux (5/1 ratio), and all data were reduced using the fundamental parameters algorithm of Rousseau (1989). Concentrations for the
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trace e l e m e n t s Ba, Th, U, Ta, Hf, Zn, Sc, Cr, Co, and Ni as well as all the R E E were d e t e r m i n e d by I N A A using reactor and counting facilities at the U n i v e r s i t y of M i c h i g a n . E s t i m a t e d uncertainties for the X R F are _ 2% or better and those for I N A A fall b e t w e e n ___1 (La) and _ 3% (Lu).
A.3. Secondary ionization mass spectrometry M i n e r a l trace e l e m e n t c o m p o s i t i o n s w e r e determ i n e d with a C a m e c a I M S - 3 f ion m i c r o p r o b e at the W o o d s H o l e O c e a n o g r a p h i c Institution. T h e analytical p r o c e d u r e s for this i n s t r u m e n t are described by S h i m i z u and L e R o e x (1986) and references therein.
A.4. Thermal ionization mass spectrometry (TIMS) After standard dissolution and c o l u m n p r o c e d u r e s described by M u k a s a et al. (1987, 1991), each sample was dried to a solid, treated with a drop of 14 N H N O 3, re-dried and then loaded on appropriate filam e n t s (single r h e n i u m for Pb, Sr, and Rb, and triple t a n t a l u m - r h e n i u m - t a n t a l u m for N d and Sm). L e a d was loaded with a silica g e l - p h o s p h o r i c acid solution, Sr with t a n t a l u m tetrachloride, and Rb, S m and N d with a 10% nitric acid solution. T h e samples were run on V G Sector t h e r m a l ionization mass s p e c t r o m e t e r s at the U n i v e r s i t y of M i c h i g a n . L e a d isotopic c o m p o s i t i o n s are corrected for fractionation using a factor of 0.12 _+ 0.02% per atomic mass unit, b a s e d on replicate analyses of N I S T Standard N B S 981. N d and Sr ratios w e r e n o r m a l i z e d to 146Nd/ 144Nd = 0 . 7 2 1 9 0 0 and 86Sr/88Sr = 0.119400, respectively. M e a s u r e m e n t s for the N I S T Standard S R M - 9 8 7 give 87Sr/86 Sr = 0.710245 _+ 10, and for the L a Jolla N d Standard values of 143Nd/144Nd = 0 . 5 1 1 8 4 2 _+ 10. Total blanks a v e r a g e d 0.04 ng for Pb, 0.02 ng for U, 0.02 ng for Nd, 0.02 ng for Sm, 0.07 ng for Rb and 0.1 ng for Sr.
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Lithos 48 (1999) 317-336
Evidence for Archean ocean crust with low high field strength element signature from diamondiferous eclogite xenoliths Dorrit E. Jacob *, Stephen F. Foley Mineralogisch-Petrologisches Institut, Universitiit Ggttingen, Goldschmidtstr. 1, G6ttingen 37077, Germany
Received 23 April 1998; received in revised form 18 January 1999; accepted 25 January 1999
Abstract Late Archean (2.57 Ga) diamond-bearing eclogite xenoliths from Udachnaya, Siberia, exhibit geochemical characteristics including variation in oxygen isotope values, and correlations of 6180 with major elements and radiogenic isotopes which can be explained by an origin as subducted oceanic crust. Trace element analyses of constituent garnet and clinopyroxene by Laser-ICPMS are used to reconstruct whole-rock trace element compositions, which indicate that the eclogites have very low high field strength element (HFSE) concentrations and Z r / H f and N b / T a ratios most similar to modern island arcs or ultradepleted mantle. Although hydrothermal alteration on the Archean sea floor had enough geochemical effect to allow the recognition of its effects in the eclogites and thus diagnose them as former oceanic crust, it was not severe enough to erase many other geochemical features of the original igneous rocks, particularly the relatively immobile HFSEs. Correlations of the trace element patterns with oxygen isotopes show that some, generally Mg-richer, eclogites originated as lavas, whereas others have lower 6180 and higher Sr and Eu contents indicating an origin as plagioclase-bearing intrusive rocks formed in magma chambers within the ocean crust. Major and trace element correlations demonstrate that the eclogites are residues after partial melting during the subduction process, and that their present compositions were enriched in MgO by this process. The original lava compositions were picritic, but not komatiitic, whereas the intrusives had lower, basaltic MgO contents. The HFSE signature of the eclogites may indicate that ocean floor basalts of the time were relatively close to island arcs and recycled material, which would be consistent with a larger number of smaller oceanic plates. Their composition appears to indicate that komatiitic ocean crust compositions were restricted to the early Archean which is not known to be represented among the eclogite xenolith population. 9 1999 Elsevier Science B.V. All rights reserved. Keywords: Eclogite; Siberia; Udachnaya; Trace element; High field strength element; Laser ablation ICPMS; Depleted mantle
1. Introduction Diamondiferous and non-diamondiferous eclogites are often members of the xenolith suites brought up from depths of the cratonic roots by kimberlites.
* Corresponding author
Mostly, they represent only a small percentage of the xenolith budget of a given kimberlite pipe, but sometimes they can dominate the suite, such as at the Roberts Victor mine, RSA. Although earlier studies proposed an origin of the eclogite xenoliths as deep mantle cumulates (e.g., MacGregor and Carter, 1970; Hatton, 1978), today it is generally accepted that many eclogites found in kimberlites are remnants of
0024-4937/99/$ - see front matter 9 1999 Elsevier Science B.V. All rights reserved. PII: S0024-4937(99)00034-1
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D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
subducted oceanic crust (Jagoutz et al., 1984; MacGregor and Manton, 1986; Jacob et al., 1994; Viljoen et al., 1996). Crucial for arguments in favour of this are oxygen isotopic data that show significant deviation from the value for the Earth's mantle (6180 = 5.5 + 0.4%~; Mattey et al., 1994), but which are similar to the range of oxygen isotopes observed in ophiolites (Gregory and Taylor, 1981; McCulloch et al., 1981) and modern oceanic crust. These ranges of oxygen isotope values can develop only at relatively low temperatures (Clayton et al., 1975), and so require processes at or close to the surface of the Earth. For the diamondiferous eclogite suite from the Udachnaya kimberlite pipe in Yakutia, Siberia, Jacob et al. (1994) could show that the precursors of these rocks belonged to a section of Archean oceanic crust that was altered by seawater much like oceanic crust today. Age determinations have revealed late Archean ages of 2.57 +_ 0.2 Ga (Pb-Pb method, this study) and 2.9 _+ 0.4 Ga (Re-Os method, Pearson et al., 1995b) for the suite from the Udachnaya kimberlite. Thus, these samples of diamondiferous eclogite xenoliths provide us with a unique opportunity to study the composition of Archean oceanic crust. Komatiites and basaltic volcanics in greenstone belts are considered by some authors to contain oceanic remnants (e.g., de Wit et al., 1992), but these interpretations are equivocal because in the only known non-tectonic contacts with basement, greenstone belts lie on continental crust (Bickle, 1978; Bickle et al., 1994). Interestingly, the ages of the eclogites coincide with ages of many greenstone belts and a major growth phase of the continental crust (Veizer and Jansen, 1979; Taylor and McLennan, 1985), so they may provide important information on plate tectonic processes operating in the late Archean, and help assess suggestions that the accumulation of late Archean ages may denote the change to modem tectonic processes (Condie, 1986). The eclogite xenoliths are probably the only direct samples of Archean ocean crust we have available. Further characterisation of the geochemistry and petrology of the eclogites and their protoliths will provide more information on geodynamic processes of the time, and allows comparison with greenstone belts which have been suggested to represent Archean ophiolites.
Here, we present Pb-Pb isotopic data for minerals as well as high precision trace element data by laser ablation microprobe inductively coupled plasma mass spectrometry (LAM-ICPMS) on eight diamondiferous eclogites from the Udachnaya kimberlite, Siberia, whose mineral constituents were previously wellcharacterized for major elements, Sm-Nd, Rb-Sr and oxygen isotopes (Jacob et al., 1994). All studied eclogites are small, between 5 and 9 cm in size, and all contain diamonds on the surface. All but one (sample 43) of the samples are bimineralic, apart from accessory diamond, with very fresh garnets and slightly altered clinopyroxenes. In no case was any primary minor phase observed, although it can be shown from the concentrations of Ti, Nb and Ta that one sample (43) must contain a Ti-bearing phase, probably rutile, which was not observed in thin section.
2. Analytical methods 2.1. Sample preparation and thermal ionisation mass spectrometry Clean mineral separates of both cpx and gt were made following the procedures described in Jacob et al. (1994). Lead isotopic compositions as well as Pb, Rb, and Cs concentrations were measured by isotope dilution mass spectrometry on aliquots of the same sample using a 2~ spike and a mixed spike for Rb and Cs. All three elements were chemically separated from the same mineral separate by a specially developed combined chromatographic separation scheme (Jacob and Jagoutz, 1994) using anion exchange with Dowex Agl • 8 (Pb) and cation exchange with Dowex 50W • 8 (Rb, Cs), respectively. Blank contributions are 30 pg for Pb, 15 pg for Rb, and 24 pg for Cs. All three elements were measured in ion-counting mode on a modified Mat-261 mass spectrometer in the laboratory of Emil Jagoutz at Max-Planck Institut fiir Chemie.
2.2. Laser Ablation Microprobe (LAM-ICPMS) Trace elements were analysed by Laser Ablation Microprobe (LAM) at the Department of Earth Sciences, Memorial University of Newfoundland, using
319
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
Table 1 Lead isotopic data for acid-washed ultrapure mineral separates. Blank contribution is 30 pg, errors are 2 oSample Group 2~ pb/2~ Pb 2~ Pb/2~ 2~ pb/2~ 55 cpx 55 gt 65 cpx 65 gt 77 cpx 77 gt 91 cpx 91 gt 29 cpx 29 gt 43 cpx a 43 gt a
1 1 1 1 1 1 1 1 2 2 2 2
18.80_+0.04 20.24_+0.03 17.93_+0.02 19.37_+0.06 15.66+0.02 18.55_+0.02 18.01 _+0.02 18.10 _+0.03 16.78 _+0.02 20.72 _+0.03 15.78 • 23.98 _+0.06
15.51+0.03 15.67+0.03 15.52+0.02 15.59+0.05 14.99+0.02 15.56_+0.02 15.40+0.02 15.54_+0.03 15.17_+0.02 15.61+0.03 15.01+0.01 15.82_+0.04
38.32 _+0.09 38.10+0.05 38.16_+0.04 37.73_+0.08 35.74 +0.04 37.75+0.04 37.81_+0.04 38.27 _+0.06 36.45_+0.04 38.14 _+0.06 35.52_+0.03 38.67 _+0.08
were p e r f o r m e d on p o l i s h e d thin sections. Previous electron m i c r o p r o b e analyses of Ca for both garnet and c l i n o p y r o x e n e were used as internal standards for the I C P M S analyses. N I S T S R M 612 glass, d o p e d with a p p r o x i m a t e l y 40 p p m of a large range of trace elements, was used as the external standard. Statistical analysis of the ablation characteristics for 53 e l e m e n t s in a variety of g e o l o g i c a l materials has s h o w n this to be an o p t i m a l c o m b i n a t i o n for the analysis of all the trace e l e m e n t s in minerals reported here ( L o n g e r i c h et al., 1996a). F u r t h e r details of analytical p r o c e d u r e s and settings, data reduction and the calculation of detection limits are given in ( L o n g e r i c h et al., 1996b).
aRutile-bearing sample.
3. Results a f r e q u e n c y - q u a d r u p l e d 266 n m w a v e l e n g t h N d : Y A G laser integrated with an e n h a n c e d sensitivity Fisons P Q I I + " S " I C P M S (Giinther et al., 1996). A n a l y s e s
L e a d isotopic data are p r e s e n t e d in Table 1 and Fig. 1. C l i n o p y r o x e n e s plot both left and right of the
15.8
15.6
a. o r ,gl ft. o r
15.4
15.2
15.0
14.8 15
16
17
18
19
20
21
Fig. 1. Pb-Pb isochron plot of Udachnaya eclogites. 2~176 error bars are smaller than sample symbols. Open circles and open squares are clinopyroxenes which are connected by tielines with coexisting garnets (filled symbols). The regression (heavy line) through the clinopyroxenes, which host 90% or more of the rocks' total lead budget, yields an age of 2.57 _+0.2 Ga. Excluded from this regression are the rutile-bearing sample and that with less than 80% Pb in cpx (squares). The Geochron, as the locus of all points that have developed undisturbed since the formation of the Earth, is shown and is contoured with /x-values (/x = 238U/204 Pb).
D.E. Jacob, S.F. Foley /Lithos 48 (1999) 317-336
320
G e o c h r o n , w h i c h d e f i n e s t h e l o c u s o f all p o i n t s w i t h
f r o m t h e R o b e r t s V i c t o r M i n e , R S A p l o t to t h e l e f t
undisturbed lead isotopic evolution since the forma-
of the
Geochron
tion of the Earth.
Pb-Pb
isotopic compositions
In contrast,
the majority
of cpx
(Jacob
and
Jagoutz,
1994).
The
of the clinopyroxenes
Table 2 Clinopyroxene compositions in the Udachnaya eclogites. Major elements in weight percent by electron microprobe, 6:80-values and data with asterisks (measured by isotope dilution) are from Jacob et al. (1994). Mg-number = 100 M g / ( M g + Fe). All other trace element data are measured by LAM and given in parts per million Group SiO 2 A1203 FeO total MgO CaO NazO Total Mg-number Cs* Rb* Th U Nb Ta La Ce Pb* Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Sc Ti V Cr Mn Co Ni Cu Ga 618 O (%o)
55 cpx 1 56.54 9.92 4.52 9.69 12.27 6.29 99.23 79.2 n.m. 0.152 0.013 0.003 0.44 0.079 0.79 3.94 0.360 0.56 93 2.46 0.87 13.3 0.58 0.25 0.62 0.076 0.41 1.34 0.044 0.13 0.011 0.063 0.007 2270 n.m. n.m. n.m. n.m. n.m. n.m. n.m. 7.07
77 cpx 1 56.76 5.47 4.08 15.38 14.42 3.74 99.85 87.0 0.171 0.212 0.062 0.025 0.82 0.117 3.84 19.5 0.479 2.52 219 9.6 1.95 9.9 0.50 0.71 1.62 0.25 1.40 5.34 0.23 0.50 0.054 0.29 0.034 2190 197 171 743 20.6 172 4.0 9.6 6.24
91 cpx 1 56.02 5.79 5.70 14.61 13.46 3.70 99.28 82.0 0.040 0.079 0.032 0.014 0.71 0.119 2.98 14.2 0.188 1.75 215 7.23 1.94 21.4 1.24 0.70 1.67 0.27 1.38 5.04 0.21 0.52 0.053 0.37 0.037 2950 199 430 780 28.2 204 7.3 12.3 7.26
29 cpx 2
43 cpx 2
68 cpx 2
56.57 10.10 2.84 9.94 14.59 5.75 99.80 86.2 0.092 0.028 0.003 < 0.002 0.24 0.040 0.82 3.92 0.176 0.63 227 2.73 0.43 5.45 0.42 0.146 0.24 0.017 0.057 0.25 0.009 0.017 0.002 0.005 0.001 7.6 2150 152 308 136 30.5 216 8.9 16.4 5.59
56.67 12.19 3.19 8.02 12.31 7.08 99.46 81.8 < 0.022 0.13 0.003 0.024 0.089 0.002 0.69 3.56 0.170 0.51 208 3.08 0.37 4.13 0.37 0.139 0.25 0.023 0.079 0.24 0.010 0.019 0.003 0.016 0.005
56.69 9.48 2.75 10.38 15.16 5.57 100.03 87.0 n.m. n.m. 0.038 0.009 0.183 0.039 1.26 4.12 n.m. 0.60 178 2.19 0.44 4.92 0.29 0.19 0.38 0.038 0.156 0.37 0.007 0.057 0.012 0.013 0.006
3000 n.m. n.m. n.m. n.m. n.m. n.m. n.m. 5.69
2610 347 328 167 19.9 409 6.8 13 n.m.
D.E. Jacob, S.F. Foley/ Lithos 48 (1999) 31 7-336
yield a 2.57 k 0.2 Ga isochron age (Fig. 1). This appears younger than, but is in fact within the error
32 1
of an age obtained by Re-0s isotopes of 2.9 f 0.4 Ga (Pearson et al., 1995b) on different eclogites
Table 3 Garnet compositions. Major elements in weight percent, 6180-valuesand data with asterisks (measured by isotope dilution) are from Jacob Fe). All other trace element data are measured by LAM. Mn data by LAM given where et al. (1994). Mg-number = 100 Mg/(Mg available, MnO is by electron microprobe
+
Group SiO, FeO total MnO
MgO CaO Na,O Total Mg-number
Ca* Rb* Th U Nb Ta La Ce Pb* Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Sc Ti
55 gt 1 40.84 22.65 14.97 0.33 14.98 5.75 0.30 99.82 64.1 0.144 0.048 0.002 0.007 0.32 0.034 0.025 0.23 0.013 0.080 0.82 0.68 0.76 25 .O 0.42 0.4 1 1.65 0.38 3.1 20.8 0.78 2.62 0.39 3 .o 0.43 2360
v Cr Mn Co Ni Cu Zn Ga 6' 0 (%o>
6.71
65 gt 1
77 gt 1
91 gt 1
29 gt 2
43 gt 2
68 gt 2
84 gt 2
D.E. Jacob, S.F. Foley / Lithos 48 (1999) 317-336
322
from the same locality. All samples except for one rutile-bearing eclogite are strictly bimineralic with garnet and clinopyroxene, the latter generally containing > 90% of the total lead. The Pb isotopic composition of the clinopyroxenes, therefore, is taken to represent the clean whole rock in preference to analyses of powdered rock material, because wholerock analyses of xenoliths have been shown to be dominated by infiltrated kimberlitic material of distinct isotopic composition (Zindler and Jagoutz, 1988). The rutile-bearing sample and that with more
than 20% of Pb in garnet were excluded from the regression, resulting in a small mean squared weighted deviation (MSWD) of 0.2, which is an indicator for the scatter of the data points. If all clinopyroxenes are included in the regression, the age changes to 2.76___ 0.15 Ga (MSWD = 9), whereas if the garnet compositions are included in reasonable modal amounts, the resulting age is 2.51 ___0.12 Ga (MSWD = 0.33) for six samples, or 2.59 + 0.11 Ga (MSWD = 1.2), if all eight samples are considered. The clinopyroxene-isochron intersects
100
Clinopyroxenes 10
/
0.1
0.01
[•
I
!
Z
V,
I..
I
i
i
~
t',-
I
:
i
1
,
:
i
i
~
'
,d
100 Garnets
10
0.1
0.01
.
.
.
.
.
[.,,
Fig. 2. Spidergrams normalized to primitive mantle (Sun and McDonough, 1989) for (a) clinopyroxenes and (b) garnets from diamondiferous eclogites from Udachnaya, Siberia. Symbols: crosses = sample 55; hatched crosses = sample 91" circles = sample 77; diamonds = sample 29; squares = sample 43; triangles = sample 68.
323
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336 the g e o c h r o n b e l o w t h e m i d - o c e a n r i d g e b a s a l t s ( M O R B s ) f i e l d at /~ = 7.9, w h e r e /x is t h e 2 3 8 U /
data for Rb, Cs and Pb w h e r e L A M
2~
available. Major element concentrations measured by
r a tio o f t h e s o u r c e in this m o d e l . Detection limit-filtered LAM
trace element data
f o r c l i n o p y r o x e n e s a n d g a r n e t s are g i v e n in T a b l e s 2
a n d 3, r e s p e c t i v e l y , c o m b i n e d w i t h i s o t o p e d i l u t i o n
electron microprobe contents
in
the
data were not
a r e a l s o listed. T r a c e e l e m e n t
studied
samples,
as
depicted
Table 4 Recalculated whole-rock compositions using equal modal proportions of cpx and gt Sample Group SiO 2 A1203 FeO total MnO MgO CaO Na20 Mg-number Cs* Rb* Th U Nb Ta La Ce Pb* Pr Sr Nd Sm Zr Hf Eu Gd Tb Dy Y Ho Er Tm Yb Lu Sc Ti V Cr Mn Co Ni Cu Zn Ga
55 WR 1 48.69 16.29 9.75 0.16 12.34 9.01 3.30 69.3 0.10 0.007 0.005 0.381 0.057 0.405 2.08 0.188 0.32 47 1.57 0.82 19.16 0.50 0.33 1.13 0.23 1.76 11.07 0.41 1.37 0.201 1.53 0.219 30 2315 146
77 WR 1
91 WR 1
29 WR 2
49.36 14.28 6.83 0.20 18.33 8.74 1.98 82.7 0.109 0.292 0.032 0.019 0.575 0.076 1.927 9.85 0.280 1.29 109 5.11 1.24 12.72 0.36 0.48 1.44 0.32 2.26 14.79 0.55 1.88 0.269 1.89 0.321 33 2485 194 186 1364 30.8 102 3.9 14 9.4
48.73 14.19 9.85 0.17 16.29 8.24 1.99 74.7 0.032 0.065 0.021 0.008 0.479 0.072 1.506 7.22 0.100 0.90 108 3.87 1.25 22.83 0.90 0.52 1.55 0.33 2.13 12.91 0.50 1.62 0.248 1.72 0.274 32 2740 185 396 1264 35.1 117 5.3 41 9.8
48.62 16.23 7.84 0.13 11.39 12.53 3.00 72.1 0.062 0.045 0.004 0.010 0.249 0.036 0.430 2.20 0.095 0.40 114 2.19 0.68 9.40 0.38 0.35 0.75 0.13 0.80 3.68 0.15 0.38 0.052 0.37 0.053 22 2510 146 310 679 50.7 124 6.9 110 14.1
43 WR 2 (Ru-bearing) 48.37 17.27 9.02 0.15 9.36 11.79 3.67 64.9 0.039 0.081 0.003 0.023 0.096 0.003 0.374 2.12 0.090 0.37 105 2.66 0.90 9.93 0.40 0.49 1.23
0.22 1.34
6.21 0.24 0.66 0.088 0.60 0.083 24 3350 260
68 WR 2 48.77 16.18 7.33 0.15 12.37 12.16 2.91 75.1
0.026 0.012 0.183 0.022 0.641 2.21 0.36 9O 1.68
0.69 7.52 0.28 0.34 0.73 0.11 0.68 3.52 0.14 0.47 0.069 0.49 0.069 23 2795 242 330 818 37.7 237 4.8 39 11.1
in
324
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
Fig. 2a and b, are all well within the range for eclogitic minerals from Siberia as well as from South Africa, except for Pb which are lower than in South African eclogites" Pb concentrations measured by isotope dilution mass spectrometry range between 0.170 and 0.479 ppm for cpx and 0.010 and 0.137 ppm for garnets. These data contrast with higher Pb contents of Southern African eclogites from the Roberts Victor and the Orapa mines for both cpx, where Pb concentrations range between and 0.05 and 1.65 ppm, and especially for garnets, which range between 0.09 and 0.184 ppm (Kramers, 1977, 1979; Smith, 1983; Jacob and Jagoutz, 1994). Mineral data are used to estimate whole rock compositions based on equal proportions of garnet and clinopyroxenes (Table 4). On the basis of these trace element results, and of previously published 618O values (Jacob et al., 1994), it is possible to identify two groups of trace element patterns corresponding to rocks with specific former stratigraphic positions within the oceanic crust (Tables 4 and 5): The first group with 6180 > 5.5%0 (i.e., higher than the mantle value of 3180 = 5.5 40.4%0; Mattey et al., 1994) and lower CaO in garnet (average CaO content 4.5 wt.%), higher abundances of heavy rare earth elements (HREE), low L a / L u ratios in garnet and no positive Eu-anomalies, whereas the second group has 6180 < 5.5%0, and shows higher average CaO in garnet of 9.9 wt.%, flat HREE patterns in garnet, higher L a / L u ratios and positive Eu-anomalies. Further characteristics are on average higher Y but lower V concentrations in garnets of Group 1 and higher Zr concentrations in cpx of Group 1. The average Z r / H f ratio in Group 1 garnets is 61, compared to 38 in Group 2 garnets
Table 5 Average characteristics of Group 1 and Group 2 eclogites Group 1, 6180 > 5.5%c
Group 2, 6180 < 5.5%0
Samples 55, 91, 77, 65 High HREE in gt, low L a / L u No positive Eu-anomaly Average CaO in gt = 4.5 Average Y in gt = 26 Average V in gt = 79 Average Zr in cpx = 15 Average Z r / H f in gt = 61
Samples 29, 43, 68, 84 Flat HREE in gt, high L a / L u Positive Eu-anomaly Average CaO in gt = 9.9 Average Y in gt = 9 Average V in gt = 115 Average Zr in cpx = 5 Average Z r / H f in gt = 38
(Table 5). By analogy with modem oceanic crust and ophiolites, we suggest that the first group corresponds to the uppermost few hundred meters of altered ocean crust, whereas the second group represents deeper levels of the crust which underwent alteration at higher temperatures (see below).
4. Discussion 4.1. The case f o r Archean oceanic crust
Oxygen isotopes have a key role in deducing a near-surface origin of eclogites brought up from mantle depths, since they are the principal indicators of processes having occurred at near-surface conditions and not those of the mantle. The pressure dependence of oxygen isotopic fractionation is very small ( < 0.2%o; Clayton et al., 1975), whereas fractionation as a function of temperature is well-known: fractionation at low temperatures is significant, whereas fractionation at mantle temperatures is very restricted. Mattey et al. (1994) showed that the average oxygen isotopic composition of clinopyroxene in peridotite xenoliths is 6180 = 5.57 _+ 0.36%0; the majority of all known 6180 data for eclogites, however, fall outside this peridotite range. Fig. 3 shows all published 6180 data for eclogite xenoliths compared to 6180 data from modern ophiolites. Although high 618O-values could be generated by metasomatic processes, radiogenic isotopes preclude this possibility for the samples studied. Incompatible trace elements are highly enriched in metasomatic fluids or melts, and their distinct isotopic signature can overprint the signature of the host rock even if the metasomatic agent has < 5% of the mass of the rock it infiltrates. Oxygen, however, is the most abundant element in the rocks, and so cannot be influenced strongly by such events. Furthermore, metasomatic events originating in the mantle will occur at temperatures in the order of 1000~ which is too high to produce the oxygen isotope fractionation seen in the eclogites. There is, however, a striking similarity between the oxygen data on eclogites and the range of 6180 data in modern ophiolites and MORB which have been subjected to hydrothermal alteration (Fig. 3).
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
Ophiolites
325
~,ffverage mantle peridotite /
"
Eclogites
1
I
I
I
I
!
I
1
1
I
I
I
I
I
Fig. 3. Ranges of published 6180 data for eclogite xenoliths suites from various kimberlites in Siberia and South Africa compared with 6180 data for modern day ophiolites. The average oxygen isotopic composition of clinopyroxene in unaltered peridotite is indicated as 5.61 _+ 0.32 (Mattey et al., 1994). Note that all eclogite suites show ranges of 6180 far outside the mantle value, but similar to the ranges in modern day ophiolites. (Data sources: Udachnaya: Jacob et al., 1994; Snyder et al., 1997" Mir: Beard et al., 1996; Orapa: Viljoen et al., 1996; Bellsbank: Neal et al., 1990; Roberts Victor: MacGregor and Manton, 1986; Semail ophiolite: Gregory and Taylor, 1981" Macquarie Island ophiolite: Cocker et al., 1982.)
Further evidence supporting a low-pressure origin of many eclogite xenoliths are positive Europiumanomalies, as can be found in eclogitic garnets and sometimes in coexisting clinopyroxenes from xenoliths (e.g., Jagoutz, 1986; Smyth et al., 1989; Caporuscio and Smyth, 1990). These positive Europiumanomalies, together with the presence of kyanite and even corundum in some eclogites, imply metamorphic growth of the eclogitic assemblage from a plagioclase-rich precursor, which could not originate under deep mantle conditions. Whereas these factors indicate an oceanic crustal origin for the eclogites, age determinations of 2.7-2.9 Ga (Jagoutz et al., 1984; Pearson et al., 1995b; this study) argue for a late Archean age of this oceanic crust. Furthermore, the coincidence of late Archean ages for eclogite xenoliths from the roots of different
continents may indicate a common origin for eclogites at this time. 4.2. Modern seawater alteration of the oceanic crust and constraints for seawater alteration in eclogites
The range of 61go-values observed in ophiolites and modern oceanic crust is due to alteration of the rocks by circulating seawater at a range of temperatures. The degree of alteration is mainly controlled by temperature, seawater/rock ratio and the composition of the unaltered rock. Although the overall geochemical effects can vary in detail between localities due to variations in rock porosity and temperature, they are generally systematic (e.g., Muehlenbachs, 1986; Alt, 1995). In the uppermost part of the altered crust, oxygen isotopic ratios are generally elevated compared with the values for unaltered
326
D.E. Jacob, S.F. Foley / Lithos 48 (1999) 317-336
basalt due to cold seawater alteration (> 2~ whereas the dike section is altered at greenshist to amphibolite facies conditions (< 450~ and decreased in 618O-values. A straightforward comparison of the major and trace element concentrations in eclogite xenoliths with those in altered oceanic crust is, however, inadequate, since eclogite xenoliths have also experienced subduction, dehydration and possibly loss of a melt component since ocean-floor alteration. In contrast to altered oceanic crust, eclogite xenoliths contain very little H20 (in the range of 0 to 86 ppm; Bell and Rossman, 1992). Assuming that this reduction in H20 content is due to dehydration during subduction, the same process would also have removed most secondary water-bearing minerals and, therefore, possibly much of their original geochemical alteration signatures due to element mobility in water-rich fluids (Brenan et al., 1995; Keppler, 1996; Stalder et al., 1998). Nevertheless, many trace and major elements measured in the eclogites correlate rather well with 6180-values. Since the range of 6180-values is undoubtedly caused by seawater alteration of the eclogite protoliths, we think it is sensible to assume that correlations of other elements or elemental ratios with 6180 are similarly generated during seawater alteration and have largely survived subsequent metamorphic overpinting, remaining relatively undisturbed through time. Typically, seawater alteration in the two temperature regimes described above generates two-winged patterns in diagrams of element concentrations or element-element ratios vs. 6180 values (Figs. 4 and 5), with the degree of alteration generally increasing towards the "tips" of the "wings". However, the trends are not necessarily very well-defined (Jacob et al., 1998a, Fig. 1) because of the heterogeneous nature of the alteration process and the complicated metamorphic history that followed. It should also be noted that samples that have 618O-values close to the "fresh" value are not necessarily unaltered, but can also represent rocks for which the hot fluid in the hydrothermal systems was in equilibrium with the rock in terms of oxygen isotopes. In this case, these samples need not plot on one of the wings. Figs. 4 and 5 are examples of some of the twowinged trends that are observed in this suite of
25 20
.E
15
9
5
~D
t.l., 0
5
5.5
6
6.5
7
7.5
8
8~O in garnet Fig. 4. FeO concentrations in garnets vs. 6180-ratios: the wingshaped pattern results from seawater alteration, modifying 6180 towards higher values under low temperature conditions and towards low 6180 under higher temperatures from initial values close to mantle. Dashed line represents 6180 of unaltered MORB.
Udachnaya eclogites. The trends formed by the lowtemperature altered sample suite and the hydrothermally altered sample suite in Figs. 4 and 5 meet in the area of 618O-values for unaltered modern oceanic crust (5.8%0). Interestingly, the slope of the two wings is different in Fig. 5. A marked two-winged pattern is also visible in a plot of FeO vs. 6180 for eclogitic xenolith garnets worldwide (including inclusions in diamonds; Jacob et al., 1998a, Fig. 1), showing a global relevance. By plotting elements or element ratios vs. 6180 as a seawater alteration indicator, it is also possible to constrain the limits of the alteration effects and to recognize elements which were immobile and therefore do not correlate with 61SO-values. In this way, it can be shown that, e.g., Ti, remained immobile in the studied rocks.
4.3. Reconstruction of whole-rock compositions For the purpose of comparing diamondiferous eclogites with ocean-floor and island-arc basalts in this paper, we calculated "clean" bulk compositions using mineral analyses and assuming equal modal amounts of garnet and cpx (Table 4). To recalculate "clean" whole-rocks is a permissible method in the field of mantle xenoliths which have been subjected to pervasive metasomatism by kimberlite during ascent, because measured whole-rock compositions for incompatible elements never represent true xenolith
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336 0.40
(Table 4), and are comparable to values from eclogite xenoliths where rutile coexists with garnet and cpx (D. Jacob, unpublished data). Although rutile was not observed in sample 43, these observations are strong evidence for its presence, and so we exclude sample 43 from the interpretations of trace elements based on reconstructed whole-rock compositions.
0.30
9~
0.20
0.10 0
L 5
5.5
6
6.5
327
7
~JsO in garnet
4.4. Similarities and differences to modern oceanic basalts
Fig. 5. L a / L u ratios representing the slope of the REE patterns vs. 6180. The high 6180-group altered at low temperatures shows
a flatter REE pattern than the low 6180-group that was altered at higher temperatures. Dashed line represents 6180 of unaltered MORB.
compositions, but rather mixtures of the xenolith with kimberlitic host material. Unfortunately, the samples were too small for exact modal analyses and it could be suspected that the calculated "clean" bulk concentrations of some trace elements are a function of error in estimation of the mode. However, test calculations showed that the trace element contents of the "clean" bulk rock are rather robust to variations of the mode within sensible limits for bimineralic eclogite xenoliths, which mostly vary between 70 to 30 modal % of garnet. Choice of the correct garnet/cpx ratio is more critical for the major elements with possible consequences for interpretation of the petrological identity of the protolith. We use 50:50 mode reconstructions of whole-rock compositions in most of the ensuing discussion, pointing out where this could be a source of error. Another source of possible error which needs to be discounted is the possible presence of rutile in eclogites, which would severely falsify the calculated abundances of high field strength element (HFSEs; Ti, Nb, Ta, Zr, Hf) in the recalculated bulk rocks. Titanium concentrations (by LAM) are between 0.215 and 0.295 wt.% for cpx and between 0.190 and 0.298 wt.% for gt, except for sample 43, whose concentrations of Ti are significantly higher (0.300 wt.% in cpx, 0.370 wt.% in gt). Furthermore, Nb and Ta concentrations in the reconstructed whole-rock from this sample (50% cpx + 50% garnet assuming no rutile) are much lower than those in other samples
4.4.1. Major element composition and petrological identity of the protoliths The reconstructed whole rocks (based on 50% each of garnet and cpx; see Section 4.3) are broadly basaltic and their average composition is marginally picritic (MgO = 9.4-18.3, average 13.4). Mg numbers range from 65-83 with an average of 73.1. This is remarkably similar to the composition reconstructed from mineral inclusions in diamond by Ireland et al. (1994). The Udachnaya eclogites show some distinction in major elements between the groups defined in Table 4. The average of Group 2 eclogites has higher CaO and A120 3, but lower MgO (11.0%) and Mg number (70.7). This is the group with lower 6180 corresponding to deeper levels of the crust, indicating that the protoliths were probably plutonic. Together with the positive Sr and Eu anomalies in the incompatible element patterns (see below), these chemical features argue for high modal plagioclase in the protoliths, which were probably gabbros, having accumulated plagioclase relative to their parental melt compositions. The average of the Group 1 eclogites has higher MgO (15.7%) and Mg number (75.6) and thus corresponds broadly to picrites. As argued above, only one of the six eclogites is rutile-saturated, so the calculated low TiO 2 contents of 0.39-0.47% for these five samples are real. On a plot of A120 3 vs. TiO 2, the eclogites are distinctly different from MORB and ocean island basalts because of these low TiO 2 contents (Fig. 6). Komatiites have similarly low TiO 2, but also have much lower A1203, and lie together with some Archean basalts on a trend towards the origin from an inflection at approximately 0.9% TiO 2 and 15% A120 3 in
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
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lm
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0
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~
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TiO2 Fig. 6. A1203 vs. TiO 2 plot of reconstructed whole rocks (solid circles) compared with modern volcanics from oceanic settings and Archean basalts and komatiites. Solid squares represent eclogite whole-rocks plus 20% tonalite melt to indicate likely protolith composition prior to melting in the subduction zone. this diagram. In Fig. 7, the eclogites are compared to various volcanic rock types from modern island arc settings. They are distinct from boninites and arc picrites, but are similar to low-K arc tholeiites. The position of the Group 2 eclogites indicates that plagioclase accumulation is only minor, since they lie well within the field of low-K tholeiites and are not similar to high alumina basalts, whose compositions are considered to be due to plagioclase accumulation (Crawford et al., 1987). Rudnick (1995) showed that eclogite xenolith SiO 2 contents generally are markedly lower than those of Archean volcanics, and attributed this to loss of a silica-rich melt during subduction. The Udachnaya eclogites, however, have relatively high SiO 2, so it cannot be ascertained simply whether or not they are residues after melt loss. In order to consider this more closely, we indicate in Figs. 6 and 7 what the compositions may have been prior to melting. Melting of basalt during subduction can be modelled as a result of recent experimental studies. Melts in equilibrium with eclogite are quartz-dioritic through tonalitic to trondhjemitic in composition (Rapp and Watson, 1995; Klein et al., 1997). Since the geotherm in subduction zones is low, melting at deep levels is
more likely than shallow level melting, so the 27 kbar, 1100~ melt composition of Rapp and Watson (1995) has been chosen to "restore" the eclogites to their possible protolith compositions. The degree of melting is uncertain, but SiO2-rich melts are relatively viscous and so difficult to segregate from their source rocks in geologically realistic timeframes at low degrees of melting (Wickham, 1987). Degrees of melting of 20-30% may be the most realistic, and so the pre-melting compositions of the eclogite protoliths calculated by adding 20 and 30% melt to the eclogite compositions are plotted in Figs. 6 and 7. The restored protoliths plot among the A1203-richer (and Mg-poorer) members of modem arc picrite suites in Fig. 7. Reconstruction of the protolith compositions reduces MgO content and Mg number appreciably relative to the eclogites, but has little effect on SiO 2 (48.8 ~ 50.8%) and A120 3 (15.7 ~ 16.0%). The average MgO content drops to 11.2% with 20% melt restoration and to 10.2% with 30% melt, whereby the lavas (Group 1 eclogites) remain marginally picritic (9.4-15.2% MgO). The Mg number of the lavas drops into the range 71-68. The high MgO of the eclogite whole-rocks relative to modern oceanic basalts could be due to either
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0
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TiO2 Fig. 7. A120 3 vs. TiO 2 plot of reconstructed eclogite whole rocks compared with volcanics from island arc settings: low-K island arc tholeiites (S. Eggins, unpublished), boninites (Jenner, 1981), arc picrites (Eggins, 1993) and high alumina basalts (Crawford et al., 1987). Filled circles are eclogite whole-rocks, and squares eclogite with 20% added tonalite melt to indicate likely pre-subduction protolith composition.
a primary picritic composition or to melt loss during subduction. The two possibilities should be differentiable by the recognition of trends caused by crystal fractionation (Mg, Fe, Ca) in the former case and by melt extraction (Si, A1) in the latter. The following geochemical and petrological points may be taken together to indicate that the eclogites are residues after melting in the subduction zone. (1) The Mg number of the eclogite whole-rocks is too high to correspond to their MgO contents if the rocks represent primitive or fractionated melt compositions. An elevated Mg number for some samples could be due to accumulation of olivine, but this process would quickly cause a significant increase in whole-rock nickel contents, which is not observed; the Ni contents of 102-237 ppm correspond to fractionated compositions (Table 4). Loss of a silica-rich melt during subduction is a viable alternative explanation: it could cause high Mg numbers but would lead to only a slight increase in Ni content of the residue due to its compatible behaviour. (2) The trends within the eclogites in major element oxide plots are not related to differing degrees
of melt loss but may be explained by crystal fractionation. The trend within the upper-level eclogites is not governed by olivine fractionation or accumulation, nor by a combination of olivine and spinel, which are the likely liquidus minerals in picritic melts (Cox, 1980; Eggins, 1993). A combination of olivine and clinopyroxene may explain the trend, which implies crystallisation from a basaltic rather than a picritic melt composition. (3) Sr and Eu contents indicate plagioclase accumulation in the lower level eclogites (see below). If fractionation of plagioclase alone is to explain the trend in the unrestored eclogites, a plagioclase of An85 is required, whereas fractionation from the restored eclogite + tonalite melt requires A n 7 5 _ 6 8 . Picrites do not crystallise plagioclase, and the Ancontent is consistent with fractionation from basalt. (4) The Udachnaya eclogites do not contain quartz or coesite (this is generally true of eclogite xenoliths in kimberlites), whereas large orogenically emplaced eclogite bodies generally do. This may be explained by the loss of a silica-rich melt component during subduction.
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4.4.2. Trace element compositions To speculate about the trace element composition of the eclogite precursors, later processes which could have affected them have to be recognized. Possible infiltration by kimberlite within the Earth's mantle can be excluded by using a "clean" bulk composition of the eclogites, reconstructed from mineral analyses and modal composition. However, the chemical changes connected with subduction (or its Archean equivalent) of the altered oceanic crust into depths of the diamond stability field are less well-known. Dehydration reactions must have occurred, and the depletion in LILE in the studied samples (Fig. 2a-b) is almost certainly a result of this, and melting of the rocks during subduction must be considered. Nevertheless, these processes could have had only limited effects, since they did not erase the seawater alteration imprint, i.e., the correlations with 6180-values. Because these correlations survive, the effects of secondary processes on the eclogite chemical composition can be relatively well-constrained. A recent experimental study by Rapp et al. (1999) supports the view that partition
0.01
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coefficients for HFSE between eclogite and coexisting melt are very close to unity. The incompatible trace element patterns normalised to primitive mantle (Fig. 8) clearly reproduce the two groups of samples defined in terms of oxygen isotope correlations (Table 5). Group 1 samples, interpreted as being from the upper crustal section, have higher levels of REE, especially visible in the HREE, whereas the Group 2 samples (from deeper in the crust) have lower levels of REE and appear to have a positive Sr anomaly. All samples show depletion in the most incompatible elements to the left of the diagram, which is probably due to remobilisation during hydrothermal alteration and subduction. The trace element abundances are lower than those in modern N-MORB with the exception of some values for Sr, Th and Ce. The lower levels than MORB towards the right side of Fig. 8 are reminiscent of the pattern for intra-oceanic island-arc tholeiites (e.g., Pearce, 1983), but the corresponding typical enrichment in the strongly incompatible elements to the left side of the diagram is missing. This,
!
!
!
!
!
!
Fig. 8. Spidergram of reconstructed whole-rock compositions, assuming equal amounts of garnet and cpx normalized to primitive mantle (Sun and McDonough, 1989). Open symbols are Group 1 (interpreted as volcanic protoliths) and filled symbols Group 2 (plutonic protoliths) as recognized on the basis of oxygen isotopes (Table 5). Group 2 has generally lower REE, positive Sr and slight positive Eu anomalies. The very low Ta and Nb of sample 43 indicate the coexistence of rutile.
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
however, is probably due to fluid loss in the subduction zone, thus effectively nullifying this enrichment by the same process which produces it in island arc volcanics. The resulting pattern is essentially flat, but with lower overall levels than MORB in Fig. 8. The HFSEs Ti, Nb, Ta, Zr and Hf are often considered to be the least mobile in geological systems. Hydrothermal mobility estimated by plotting element concentrations as a function of 6180 confirms lower mobility for the HFSE in the Udachnaya eclogites: Ti is essentially immobile, for the "volcanic" Group 1 eclogites, the immobility of Nb and Ta is shown by the lack of correlation with 6180, whereas Zr and Hf are slightly mobile, showing a weak positive correlation with 6180. In contrast, Zr and Hf were immobile in the "plutonic" Group 2 eclogites, whereas Nb and Ta were slightly mobile. These differences probably reflect variation in mobility in hydrothermal fluids at different temperatures. The trace element patterns normalised to island arc tholeiites (not shown) show that the HFSE abundances are more like those of island arc tholeiites than MORBs, although the full trace element pattern is confused due to the greater mobility of most incompatible elements (Figs. 5 and 8). The behaviour of the HFSE is better assessed in plots which are restricted to the relatively immobile HFSE (Fig. 9); only data in which Nb, Ta, Zr and Hf were all analysed by ICPMS are used in these plots. The eclogites plot to lower Z r / H f and N b / T a than low-K island arc tholeiites (S.M. Eggins, personal communication), with some overlap of Zr and complete overlap of Nb concentrations, and to much lower ratios and concentrations than Atlantic MORB (triangles; Dosso et al., 1993). Also plotted are MORBs from the Chile ridge, including low-Nb MORBs (Bach et al., 1996), those showing an island-arc-like trace element pattern (Klein and Karsten, 1995), as well as near-ridge seamounts (Niu and Batiza, 1997). The positions of the eclogites in Fig. 9 are distinct from all modern oceanic basalts, but are more similar to island arc tholeiites than to MORB. This is also consistent with the TiO 2 contents of less than 0.5 wt.%, which find analogy only among arc-related volcanics in modern tectonic settings. The REE patterns for the Group 2 samples show a positive Eu anomaly which may be due to the presence of plagioclase in the protolith (Fig. 8). Since
331
these samples are from deeper crustal levels, they may represent metamorphosed plagioclase-bearing plutonic igneous rocks such as gabbros. Aluminiumricher eclogites with positive europium anomalies and high 6180, representing upper oceanic crust, were described from Roberts Victor, South Africa (Jagoutz et al., 1984). Positive Eu-anomalies in the upper part of the oceanic crust are unlikely to be due to plagioclase accumulation. However, black smoker vent fluids have huge positive Eu-anomalies (Edmond et al., 1982), so diffuse hydrothermal alteration may cause Eu anomalies in uppermost crustal samples. Eu anomalies may thus indicate primary crustal signatures; their generation during subduction would require reducing conditions which do not correspond to most estimates of the prevailing conditions. 4.5. Geodynamic aspects of Archean ocean crust composition 4.5.1. The composition of the Archean ocean crust The following petrological scenario may explain the genesis of these rocks, based largely on the characteristics of the "volcanic" Group 1 eclogites. The eclogites represent residua after melting in the subduction zone. The protolith was either high-Mg basalt or marginally picritic and became more Mgrich by the extraction of a silicic melt component during subduction. The HFSE signature was largely unaffected by this process and is distinctly different from that of modern MORB. The HFSE and AlzO3/TiO 2 abundances and ratios are most similar to island arc basalts among modern oceanic igneous rocks (Figs. 6, 7 and 9). Alternative scenarios in which the low HFSE characteristics are produced during hydrothermal alteration or subduction metamorphism of a MORBlike basalt or picrite protolith are considered unlikely because they require the preferential mobilisation of the HFSE. This lacks a modern analogy among hydrothermally altered ocean crust, and the HFSE should be either concentrated or unaffected by dehydration or melting of oceanic crust during subduction (Brenan et al., 1995; Keppler, 1996; Stalder et al., 1998). The eclogite compositions in Table 4; Figs. 6 - 9 depend on the assumption of 50% cpx and 50% garnet for the whole-rock reconstruction. Petro-
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+
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'
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'
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Fig. 9. HFSE concentrations and ratios for the reconstructed eclogites compared to modern oceanic and arc basalts. Symbols: Group 1 eclogites= filled circles; Group 2 eclogites=open circles; filled triangles= North Atlantic MORB (Dosso et al., 1993); shaded field = island arc low-K tholeiites (S. Eggins, unpublished); open triangles = low-Nb MORBs (Bach et al., 1996); crosses = Chile ridge MORB with island arc trace element signature (Klein and Karsten, 1995); open field = pacific seamounts (Niu and Batiza, 1997). The filled circles in the Z r / H f plot represent eclogites in which these elements are least mobile according to element/oxygen isotope correlations. The eclogites manifest a component with low Zr/Hf, N b / T a ratios and low concentrations, which may be a component in island arc basalts or in the Pacific seamounts.
graphic observations on a large number of eclogites suggest that garnet probably makes up more than 50% rather than less. The effect of changing the
garnet content from 50 to 70% is a decrease of average SiO 2 from 48.8 to 45.7%, Na20 drops from 2.64 to 1.96%, and Mg number from 76.7 to 73%,
D.E. Jacob, S.F. Foley/Lithos 48 (1999) 317-336
whereas FeO rises from 8.3 to 10.1%, MgO from 13.9 to 14.7%, and A120 3 from 15.5 to 18.4%. None of these variations is enough to change the main conclusions. The high A120 3 in the reconstructed whole-rock with 70% garnet could be said to lend support to high-alumina basalt as a precursor, but this is not consistent with the lower SiO2: high alumina basalts usually have in excess of 50% SiO 2, compatible with accumulated plagioclase of intermediate composition (Crawford et al., 1987). The Pb-Pb age of the Udachnaya eclogite suite is a subduction age of 2.57 Ga, indicating formation at the spreading ridge at about 2.59-2.62 Ga if we accept a younger average crustal age at subduction in the late Archean (Arndt, 1983). An increasing number of dependable age determinations of eclogite xenoliths using several isotopic systems fall consistently between 2.5 and 2.9 Ga (Jagoutz et al., 1984; Jacob et al., 1994; Pearson et al., 1995b), indicating that retrievable samples of Archean ocean crust may be limited to this period. Thus, they do not discount the much-discussed possibility of komatiitic ocean crust in the early Archean (Bickle, 1978; Arndt, 1983; Nisbet and Fowler, 1983) but their transitional basalt-picrite compositions are consistent with a steadily cooling upper mantle producing komatiite to high-Mg picrite melts in the early Archean and basalt to picrite at the end of the Archean. The major element compositions of the eclogite suite correspond to the lower limits of the range of mantle temperatures interpolated by Abbott et al. (1994) for this period.
4.5.2. Eclogites and crustal recycling The eclogites have low HFSE abundances and unusually low Z r / H f and N b / T a ratios (Fig. 9a-b). These signatures are not found among modern oceanic basalts, but the trends in Fig. 9 show that they may be present as a component in island arc tholeiites and in the east Pacific seamounts described by Niu and Batiza (1997). The involvement of eclogite as a recycled component in the genesis of oceanic basalts has often been discussed (e.g., Hirschmann and Stolper, 1996), but is usually assumed to have an enriched signature: Niu and Batiza (1997) favoured recycled eclogite as the cause for the inclined seamount trend in a N b / T a vs. Nb diagram (Fig. 9), but considered the eclogite signature to correspond
333
to the high N b / T a and Nb end of the trend, whereas they attributed the low N b / T a to unusually depleted upper mantle peridotite. A similar trend towards low N b / T a and Nb concentrations is typical of island arc basalts (Fig. 9) but is usually attributed to preferential mobilisation of incompatible elements other than HFSE in the subducted slab (Brenan et al., 1995; Pearce and Peate, 1995; Stalder et al., 1998). The HFSE characteristics of the eclogites may be attributable to either an arc-like setting or to their origin as mid-ocean ridge magmas. However, in either case, the mantle source must have been exceptionally depleted by previous melt loss, which is contrary to most expectations of progressive depletion of the upper mantle to produce the modern depleted MORB reservoir. This may be reconciled by appealing to melting of a layer of very restricted thickness at the top of the upper mantle, implying convection cells of very limited extent and rapid recycling of subducted material within the shallow convection cells. If these eclogites are typical of oceanic crust at the end of the Archean, this would be consistent with models for more numerous, small oceanic plates (Nisbet and Fowler, 1983; Hargraves, 1986) consisting of picrites and basalts which are rarely free of the influence of nearby island arcs or recycled material. This need not mean that younger, Proterozoic eclogites have the same signature, since the source region for MORB may have become progressively thicker with time, resulting in progressively less depleted ocean crust.
4.5.3. Craton formation The Udachnaya eclogites represent oceanic crust of late Archean age which was subducted and incorporated into a growing subcontinental lithosphere. Their composition contrasts with that of mid-ocean ridge basalts being subducted today, but we cannot be sure if their compositions are typical of late Archean oceanic crust, or whether they were preferentially preserved due to their proximity to continental margins. The incorporation of the subducted oceanic crust into the cratonic lithosphere and the sampling of eclogite xenoliths of late Archean age from beneath cratons which include even older continental crustal rocks probably indicates subduction beneath a continental margin. Re-Os ages for peridotites of the
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cratonic lithosphere, including U d a c h n a y a (Pearson et al., 1995a), show that they are also late Archean, although often slightly older than eclogites. The cratonic lithosphere also contains sub-calcic garnets with very high CrzO3-contents that may be explained by their formation from Cr-spinel-bearing metamorphic precursors at shallow lithosphere levels (Bulatov et al., 1991; Jacob et al., 1998b; Stachel et al., 1998). The eclogites thus appear to have been incorporated into a rapidly forming lithosphere together with other rocks of shallow origin, and shortly before the widespread age for cratonisation at about 2.5 Ga (Condie, 1989). The eclogite ages coincide with a rapid increase in continental crustal formation at the end of the Archean (Taylor and McLennan, 1985), showing this to be an era of far-reaching change in tectonic style (Condie, 1986). If this is true, then the ultradepleted HFSE-signature of the eclogites may not necessarily be characteristic of the period 3 . 0 - 2 . 5 Ga, but a legacy of an extinct Archean style of m a g m a genesis.
Acknowledgements This study was made possible by a stipendium and grant from the Deutsche F o r s c h u n g s g e m e i n schaft for D.J. W e are grateful to Steve Eggins for making his unpublished database of precise analyses of l o w - K arc tholeiites available for comparisons in the figures, and Bob Rapp for access to unpublished work. Reviews from Charles Stern, Bill M c D o n o u g h and Matthias Barth helped focus the ideas expressed in this paper. W e are grateful to Trevor Falloon, R o d e y Batiza and Bob Rapp for rapid advice in the later stages of the project.
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Author index to volume 48 Bostock, M . G . , Seismic imaging of lithospheric discontinuities and continental evolution . . . . . . . . . . . . . . . . . . . . . . . . de Smet, J.H., A.P. van den Berg and N.J. Vlaar , The evolution of continental roots in numerical thermo-chemical mantle convection models including differentiation by partial melting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Foley, S.F., see Glaser, S.M . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Foley, S.F., see Jacob, D.E . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Francis, D., see Schmidberger, S.S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Furman, T. and D. G r a h a m , Erosion of lithospheric mantle beneath the East African Rift system: geochemical evidence from the Kivu volcanic province . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Glaser, S.M., S.F. Foley and D. Giinther, Trace element compositions of minerals in garnet and spinel peridotite xenoliths from the Vitim volcanic field, Transbaikalia, eastern Siberia . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Graham, D., see Furman, T . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Giinther, D., see Glaser, S.M . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hager, B.H., see Shapiro, S.S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hager, B.H., see Shapiro, S.S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Hauri, E.H., see Stern, C.R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Jacob, D.E. and S.F. F o l e y , Evidence for Archean ocean crust with low high field strength element signature from diamondiferous eclogite xenoliths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Jaupart, C. and J.C. Mareschal, The thermal structure and thickness of continental roots . . . . . . . . . . . . . . . . . . . . . . . . . Jones, A . G . , Imaging the continental upper mantle using electromagnetic methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . Jordan, T.H., see Shapiro, S.S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Jordan, T.H., see Shapiro, S.S . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Kilian, R., see Stern, C.R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Kyser, T.K., see Stern, C.R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Mareschal, J.C., see Jaupart, C . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Mukasa, S.B. and J.W. Shervais , Growth of subcontinental lithosphere: evidence from repeated dike injections in the Balmuccia lherzolite massif, Italian Alps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Nyblade, A . A . , Heat flow and the structure of Precambrian lithosphere . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Olker, B., see Stern, C.R . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Pearson, D . G . , The age of continental roots . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Priestley, K . , Velocity structure of the continental upper mantle: evidence from southern Africa . . . . . . . . . . . . . . . . . . . . Schmidberger, S.S. and D. Francis, Nature of the mantle roots beneath the North American craton: mantle xenolith evidence from Somerset Island kimberlites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Shapiro, S.S., B.H. Hager and T.H. Jordan, Stability and dynamics of the continental tectosphere . . . . . . . . . . . . . . . . . . . . Shapiro, S.S., B.H. Hager and T.H. Jordan, The continental tectosphere and Earth's long-wavelength gravity field . . . . . . . . . . Shervais, J.W., see Mukasa, S.B . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Simons, F.J., A. Zielhuis and R.D. van der Hilst, The deep structure of the Australian continent from surface wave tomography . . . Stern, C.R., R. Kilian, B. Olker, E.H. Hauri and T.K. Kyser , Evidence from mantle xenoliths for relatively thin ( < 100 km) continental lithosphere below the Phanerozoic crust of southernmost South America . . . . . . . . . . . . . . . . . . . . . . . . . van den Berg, A.P., see de Smet, J.H . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . van der Hilst, R.D., see Simons, F.J . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Vlaar, N.J., see de Smet, J.H . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Zielhuis, A., see Simons, F.J . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 0 2 4 - 4 9 3 7 / 9 9 / $ - see front matter 9 1999 Elsevier Science B.V. All rights reserved. PII: S 0 0 2 4 - 4 9 3 7 ( 9 9 ) 0 0 0 5 0 - X
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153 263 317 195 237 263 237 263 115 135 217 317 93 57 115 135 217 217 93 287 81 217 171 45 195 115 135 287 17 217 153 17 153 17
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Subject Index Abitibi belt (Canada) heat flow 9, 95, 101-102, 107-108 Appalachians (North America) heat flow 95, 97-98, 101-102, 107 Archean Passim. Archean cratons composition 195, 214-215 heat source 112, 155 heat flow 81-90, 93-111 Archean ocean crust 317-318, 324-325, 331 Archie's Law (conductivity) 60 Asia seismic structure 6 Australian continent age 187 electrical conductivity 37, 67 heat flow 37, 93, 103 seismic structure 4, 5, 7, 17, 29-33, 3739, 54 Baikal rift 264, 282 Balmuccia Massif 287-290 Baltic shield electrical conductivity 67, 73-76 heat flow 82, 87 seismic structure 5, 38, 73-76, 87 Bastar craton (India) 103 batch melting (effect on isotope composition) 174 blocking/closing temperature (of isotope systems) 173, 180 boundary layer conductive~ 83, 105-106, 115-116, 120, 162 mechanical ~ (MBL) 155, 157, 161,237, 191 thermal~ (TBL)4, 18, 83, 105-106, 115-116, 118, 120-122, 126-129, 135-136, 167-168, 217-218, 232, 237 chemical/compositional~ (CBL) 89, 115-116, 120, 122, 126-131,153-154, 196, 237
broad-band seismology 9-10, 17-23, 45, 47-52 Bushveld complex 186-187, 191
Canadian shield composition 195, 203-205, 212-215 heat flow 93, 94-98, 101-104, 195, 212 seismic structure 5, 6, 8-9, 12, 51 Central shield (Australia) 19, 37-38, 103-104 chemical/compositional boundary layer (CBL, see boundary layer) compositional buoyancy 18, 36-37, 86, 115-116, 120, 122, 126-131, 135-136, 158 conductivity (see electrical conductivity and resistivity) continental crust 10-11, 45, 54 evolution 1, 10-13, 153, 154, 160-165, 168 heat flow 81-90, 93-111, 167 lithospheric mantle (CLM) 1, 3-5, 9-13, 18, 36-39, 45, 47-49, 53-55, 57-58, 62, 70-71, 76, 81, 83, 85-87, 89-90, 93, 115-116, 128-131, 153-154, 160165, 168, 171-175, 181, 191, 195, 214-215,217-218, 238-239, 257-258, 287-288, 310 convection 116-118, 131, 151, 153-155, 333 convective instabilities 18, 38-39, 88-89, 115-116, 126, 129, 130, 164-165 cooling (conductive) 18, 81, 83, 115-116, 126, 130-131, 135-136, 153-154, 158, 167, 217, 230-232 craton Passim. crust continental ~ 10-11, 45, 54 oceanic~ 10-11, 317-318, 324-325, 331
crustal heat production 85, 90, 93, 98-102, 104-105, 107, 109, 155, 212 resistivity 62-63, 71-73 structure (seismic) 10-11, 45, 46, 53, 54 thickness (see also Moho) 1, 2, 7, 9, 25, 46, 154
Dharwa craton (India) 103 decompression melting 54, 153-154, 158 delamination / destruction of lithosphere (see also convective instabilities) 12, 12, 88-89, 126, 129, 165, 237-238, 257258, 263 density vs. seismic wavespeed (din p / dlnVs) 135, 139, 147, 150-151 depletion (melt ~ ) 18, 38, 86, 109, 115116, 120, 136, 153-155, 158, 160-163, 167, 174, 203, 214-215, 282, 291, 317, 328-329, 333 diamond inclusions 171, 180-182 diamond stability field 195, 211-212, 330 diapiric upwellings 158 dike/dike emplacement 287-291, 312313 dynamic topography 120, 122, 126
East African rift composition 243-245, 246-251, 254257, 258 CLM thickness 257-258 crustal thickness 257-258 geodynamic setting 239-242 Eclogite 11, 13, 177-178, 190, 201, 317318, 322, 324, 325, 328-329, 333-334 electromagnetic methods (EM) 57-62 electrical asthenosphere 63-68, 76 anisotropy 58, 70-71, 76 conductivity 57, 59, 66, 68-72, 264 resistivity 57, 59, 67, 72-74
340
Fennoscandia shield heat flow 107 seismic structure 7-8, 38 fractional melting 203, 212-213 Fresnel zone 2-3 garnet peridotites 201, 209, 219-221, 231-232, 263, 264, 266 garnet stability field 264 geobarometry 210-211, 218-219, 230232, 275 geochronology isochron method 173, 176-179, 319-320 model age method 180-182 K-Ar 82 Ar-Ar 82 Pb-Pb 318-321 Rb-Sr 82, 181 Re-Os 173-174, 177-178, 182-190, 226, 234, 318, 321,334 Sm-Nd 82, 177-182 U-Pb 82, 173, 178-180, 199 U-Th-Pb 180 geoid (hydrostatic ~) 135-137, 141-143, 150-151 geoid height anomalies 115-116, 120, 122, 126-128, 131, 147 geothermal gradient 18, 37, 67-68, 76, 90, 106-109, 154-157, 195, 210-212, 217-219, 230-231 geothermometry 210-211, 218-219, 230-231,263, 275 gravity field / anomalies 115-116, 131, 135-137, 141-143, 150-151,239 Grenville Province (North America) heat flow 88-89, 93, 95, 101-102 seismic structure 38, 88-89 harzburgite/harzburgitic 155, 195, 209, 211,213, 219, 233 heat flow 93-111,125-126, 131,167, 195, 212 continental ~ 81-90, 93, 100-104 corrections 100, 107, 110-111 determination of ~ 110-111 mantle ~ 93, 100, 104-105 reduced ~ 100, 182 vs. lithospheric age 83-90, 100, 125-126, 167 vs. heat production 102-103 vs. CLM stabilization 82, 85-86, 89-90 heat production crustal ~ 81, 85, 90, 93, 98, 101-102, 105, 108-111, 155, 212 mantle ~ 154-155
Subject Index
Indian shield heat flow 82, 93, 103 isopycnic hypothesis 18, 120, 126, 128, 135-136, 150 isotope systems Hf-Os 174 Nd-Sr 174, 175,225-227, 237, 244-245, 251,306 Nd 173, 175, 180-181, 237, 242-244, 251,253 O 217, 229, 317, 324-327 Os 174, 176-177, 182-183, 188-190, 226-228 Pb 173, 174, 226, 228, 237, 253, 309310, 322 Sr 173, 175, 182, 237, 242-245, 251253, 306-307 Italian Alps 287-290 Ivrea Verbano Zone 288-290
Kaapvaal craton (Southern Africa) age 46, 171, 185-188, 191 composition 195, 204, 209, 213-215 heat flow 94, 99, 107-108 seismic structure 39, 46-47, 51, 54, 213 kimberlites 1, 4, 47, 171, 174, 176, 179, 184, 195, 198, 201,263-264, 317-318 Kola deep borehole 102 KTB deep borehole (Germany) 102
Laramide orogeny 12 lherzolite/lherzolitic 4, 155, 176-177, 195, 209, 211, 213, 219, 233, 265-268, 288, 291 garnet ~ 265 garnet-spinel ~ 265-268 spinel ~ 265-268, 291 Limpopo belt (Southern Africa) age 187 heat flow 98 seismic structure 46, 54 lithoprobe 7, 94 lithospheric mantle age o f ~ 171, 190-191, 317-319, 325, 333 base of ~ 1, 4, 9, 11-13, 47-54, 57, 67, 73-76, 105-106, 122, 219, 221,230 continental ~ (CLM) 1, 3-5, 9-13, 18, 36-39, 45, 47-49, 53-55, 57-58, 62, 70-71, 76, 81, 83, 85-87, 89-90, 93, 115-116, 128-131,153-154, 160-165, 168, 171-172, 191, 195, 217-218, 238-239, 257-258, 287-288, 310
composition 195, 196, 209-214, 221229, 233, 333-334 erosion/delamination/destruction o f ~ 12-13, 38-39, 88-89, 126, 129, 165, 217, 230-234, 237-238, 257-258, 263 evolution 37-39, 57, 76-77, 88-89, 116, 119, 128-131,153-155, 160-165, 168, 171-173, 184, 191,230-234, 258-259, 280, 282, 288, 310, 313, 333 formation 10-13, 18, 37, 57-58, 76-77, 154-156, 160-163, 171-172, 191,288, 325, 333 growth/thickening 171-172, 232, 234, 287, 333 oceanic~ 10-13, 93, 106, 115-116, 118, 153, 232-234, 239 resistivity 57-60, 62-63, 73-77 thermal structure of ~ 90, 105-110, 119-125 thickness 1, 4, 9, 17-18, 30-31, 36-39, 49, 51-52, 54-55, 62, 67, 73-76, 81, 83-87, 89-90, 93, 94, 105-110, 120, 122, 126-127, 130, 136, 153, 160-163, 168, 172, 212, 217, 219, 221, 230, 232-234, 257-259 thinning 230-234, 237-239, 257-259, 287 long period seismology 3-5, 51 Love waves (seismic surface waves) 4749, 51-54 low velocity zone (seismic) 6-7, 30, 37, 39, 47-48, 51-55 Lynn Lake belt 95
Magnesium number-(Mg#) 195, 203205, 209-214, 224-225, 268, 275, 281282, 321,327, 329 magnetotelluric imaging 57, 60-62 mantle convection (see convection) depletion 18, 109, 155, 158, 165-168, 333 differentiation 153-155, 157-158, 165166 heat flow 93, 100, 104-105 stratification 1, 4, 5-7, 9-13 massif peridotites 109, 171-173, 176, 188, 287-290 mechanical boundary layer (MBL, see boundary layer) melt depletion / extraction 86, 109, 115116, 120, 136, 153-155, 158, 160-163, 167, 174, 282, 291, 317, 328-329, 333 Mohorovicic discontinuity (Moho, M) 1, 2, 7, 9, 25, 46, 54, 154
341
Subject Index Namaqua Natal belt 46, 93, 99 Nikos kimberlite (see Somerset Island kimberlite) North American craton composition 195, 203-205, 209-214 heat flow 82, 87, 93, 95, 102, 195, 212 resistivity 69 seismic structure 5-8, 87-88
ophiolites 325 ortho-pyroxene enrichment 213-215
195, 205,
paleogeotherm 195, 211-212, 214 partial melt(ing) 37, 57, 66-67, 72-73, 86, 153-155, 203, 212, 214-215, 237238, 310, 317, 328-329, 333 effects on conductivity 66, 72 Partitioned Waveform Inversion 22-26 peridotite high temperature 173,217, 221,232-234 low temperature 173, 217, 221,232-234 massif~ 109, 171-173, 176, 188 xenolith ~ 171-174, 198, 264, 317-319 phase changes (mineralogical) 2 (see also seismic discontinuities) Pilbara (Australia) 19-20 heat flow 82, 93, 103 seismic structure 32, 36, 38 Premier mine (South Africa) 171, 177, 181, 184, 187 primitive mantle composition 203, 214 Proterozoic Passim. Proterozoic shields composition 195 heat flow 81-90, 93
radioactive decay 155 heat production 155 heat sources 155 Rayleigh waves (seismic surface waves) 17, 22, 26, 45-55, 87 reduced heat flow 100-102 reflection seismology 7-9 refraction seismology 5-7 resistivity 58-60, 62-63, 73-77 rheology 115-118, 123, 126, 128-131, 153-157 activation energy 115-117, 126, 128, 130, 131, 156 activation volume 156, 157 effects of volatiles 38, 86, 131, 157
Roots (see also continental lithospheric mantle) 55, 57-58, 69, 128, 153, 165, 171, 191, 195, 217-218 Russian platform 6-7, 9
secular (conductive) cooling 81, 83, 115116, 126, 130-131, 135-136, 153-154, 158, 167, 217, 230-234, 263 seismic anisotropy 1, 4, 7, 9, 12, 49, 51 reflection 7-9 refraction 5-7 tomography 2, 47, 52, 54, 136, 147, 195 seismic discontinuity lithospheric ~ 1 Hales (H) ~ 3-6, 9, 11-12 Lehman (L)~ 1, 3-7, 9, 12 Mohorovicic (Moho, M) ~ 1, 2, 7, 9, 46, 54 410-km~ 2, 6, 39, 68, 70, 128 520-km ~ 2 660-km ~ 2 seismological imaging long-period 3-5, 51 broad-band 9-10, 17-23, 45, 47-52 tomography 2, 17, 17-26, 39, 47, 52, 54, 136, 147, 195 Siberian craton age 171, 176-179, 186-187, 190-191, 317-319, 334 composition 195, 204, 213-214, 263, 282-283, 317, 324, 327, 329 conductivity 67, 73-74 heat flow 82 seismic structure 6-7 Sino-Korea craton heat flow 104 seismic structure 38 Skippy project 17, 19, 26 Slave Province (Canada) electrical conductivity 61, 64, 72 heat flow 64, 95, 212 seismic structure 8, 11,212-214 thermal structure 195, 210-212 Somerset Island kimberlite (Canada) 195-215 South(ern) African cratons age 171, 186-188 composition 195, 325 heat flow 82, 93-94, 98-100, 104, 110 seismic structure 45-55 South American lithosphere (Phanerozoic) composition 217, 219, 221-231, 233, 324-325
evolution 230-234 thickness 217-219, 230, 232-234 stability / stabilization (of continental lithospheric mantle) 1, 10-13, 18, 3738, 81, 85-86, 115-116, 122, 126-131, 135, 151, 153-155, 179, 184, 186, 191, 288 subduction 1, 8-13, 130, 136, 317-318, 326-329, 331,334 Superior Province (Canada) electrical conductivity 69-71 heat flow 82, 94-99, 101-102 seismic structure 8-9, 69-71 surface waves dispersion 2, 17-18, 22-23, 31, 45, 4752 fundamental modes 17-18, 22-23, 2627, 39, 45, 47-52 higher modes 17-18, 22-23, 26-27, 39, 45, 47-52 Tanzania craton 239 age 171, 178, 191 heat flow 82 Tasman line (Australia) 19-20 tectonic regionalization 17, 19, 28-29, 34-36, 136-137, 139-140, 151 tectosphere (see also continental lithospheric mantle) 4, 17-18, 34, 36-39, 115-118, 122, 128-131, 135-136, 150151, 154, 168 thermobarometry (see geobarometry, geothermometry) thinning of continental lithosphere 230234, 237-239, 257-259 Thompson belt (Canada) 95, 100, 102 trace element chemistry 226, 244, 245251, 263, 276-281, 303-306, 317, 322324, 327, 329 Trans-Hudson Province (Canada) heat flow 95, 100-102 seismic structure 6 transmitted seismic waves 2-3 Udachnaya (see Siberian craton) United States of America heat flow 94 seismic structure 128 viscosity (see also rheology) 76, 116-118, 122-123, 126-131, 154-157 viscous heating 154 Vitim volcanic province 186-187, 263264
342 volatiles effects on electrical conductivity 37, 66-67, 72-73 effects on rheology 38, 86, 131, 157 Western shield (Australia) 37-38, 103 Witwatersrand basin (South Africa) 99,
Subject Index 104-105, 186-187
Wyoming craton (North America) age 171, 186, 191 xenoliths 1, 4, 81,171-174, 179-183, 190, 195-215, 217-218, 221-231, 238, 257, 263, 265-266, 288, 317-319, 325
YUgarn (Australia) 19-20 heat flow 82, 103 seismic structure 31-33, 36, 38 Zimbabwe craton (Southern Africa) age 186 seismic structure 46, 54