Éditeur(s) : HAL CCSD Nature Publishing Group
Résumé : International audience
The mantle and continental crust--Earth's main silicate reservoirs--have a lead isotope composition that is too radiogenic to have evolved from primitive Solar System material over 4.57 billion years1. To account for this imbalance, it has been suggested that unradiogenic lead may have partitioned into the metallic core2, 3, 4 or lower continental crust5. Alternatively, radiogenic lead could have been added to Earth later by meteorite impacts6. Unradiogenic lead was discovered in fragments of mantle rocks exhumed in the Horoman massif, Japan, implying that the mantle itself may provide a complementary reservoir of unradiogenic lead7. However, it is unclear why this unradiogenic component is not sampled by the melting that generates oceanic basalts8. Here we present double-spike lead isotope data for abyssal peridotite rocks, considered to represent suboceanic mantle, exposed on the Atlantic Ocean floor. We find that sulphides dated at about 1.83 billion years old and trapped as inclusions in silicate minerals preserve extremely unradiogenic lead isotope compositions. This unradiogenic lead could have been prevented from adding significantly to oceanic basalts if either the silicates shield the sulphide inclusions or if the sulphides reside in refractory mantle rocks that are rarely sampled during melting. We conclude that the lead isotope composition of the silicate Earth could be largely balanced by unradiogenic lead in sulphide in the mantle.
ISSN: 1752-0894

hal-00795575
https://hal.archives-ouvertes.fr/hal-00795575
DOI : 10.1038/ngeo1531

Éditeur(s) : HAL CCSD Elsevier
Résumé : Differentiation of the Earth's mantle and formation of continental and oceanic crust occur principally through partial melting and extraction of basaltic melt. Among the mantle rocks occurring at the Earth's surface, as tectonically-emplaced massifs, abyssal peridotites or xenoliths, the harzburgites (< 5% clinopyroxene) are widely considered as refractory mantle residues left after extraction of a basaltic component. In contrast, the most fertile lherzolites (15% clinopyroxene) are generally regarded as pristine mantle, only weakly affected by partial melting. In this paper we present new convergent structural and geochemical data from the Lherz massif, the type-locality of lherzolite, indicating that the lherzolites from Lherz do not represent pristine mantle. Detailed structural mapping clearly shows that the lherzolites are secondary rocks formed at the expense of the harzburgites. Variations of major, minor and trace elements through the harzburgite–lherzolite contacts indicate that the lherzolites were formed through a refertilization process involving interaction of refractory, lithospheric mantle with upwelling asthenospheric partial melts. Combined with previously published indications of refertilization in orogenic peridotites, our new observations in Lherz suggest that most lherzolite massifs represent secondary (refertilized) rather than pristine mantle. Together with geochemical data on mantle xenoliths, this indicates that melt transport and melt-rock reaction play a key role on the rejuvenation and erosion of the lithospheric mantle.
ISSN: 0012-821X

hal-00406433
https://hal.archives-ouvertes.fr/hal-00406433
DOI : 10.1016/j.epsl.2007.05.026

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Highly siderophile element concentrations (HSE: Re and platinum-group elements (PGE)) are presented for gabbros, gabbroic eclogites and basaltic eclogites from the high-pressure Zermatt-Saas ophiolite terrain, Switzerland. Rhenium and PGE (Os, Ir, Ru, Rh, Pt, Pd) abundances in gabbro- and eclogite-hosted sulphides, and Re-Os isotopes and elemental concentrations in silicate phases are also reported. This work, therefore, provides whole rock and mineral-scale insights into the PGE budget of gabbroic oceanic crust and the effects of subduction metamorphism on gabbroic and basaltic crust. Chondrite-normalised PGE patterns for the gabbros are similar to published mid-ocean ridge basalts (MORB), but show less inter-element fractionation. Mean Pt and Pd contents of 360 and 530 pg/g, respectively, are broadly comparable to MORB, but gabbros have somewhat higher abundances of Os, Ir and Ru (mean: 64, 57 and 108 pg/g). Transformation to eclogite has not significantly changed the concentrations of the PGE, except Pd which is severely depleted in gabbroic eclogites relative to gabbros (similar to 75% loss). In contrast, basaltic eclogites display significant depletion of Pt (>= 60%), Pd (>85%) and Re (50-60%) compared with published MORB, while Os, Ir and Ru abundances are broadly comparable. Thus, these data suggest that only Pt, Pd and Re, and not Os, Ir and Ru, may be significantly fluxed into the mantle wedge from mafic oceanic crust. Re-Os model ages for gabbroic and gabbroic eclogite minerals are close to age estimates for igneous crystallisation and high-pressure metamorphism, respectively, hence the HSE budgets can be related to both igneous and metamorphic behaviour. The gabbroic budget of Os, Ir, Ru and Pd (but not Pt) is dominated by sulphide, which typically hosts >90% of the Os, whereas silicates account for most of the Re (with up to 75% in plagioclase alone). Sulphides in gabbroic eclogites tend to host a smaller proportion of the total Os (10-90%) while silicates are important hosts, probably reflecting Os inheritance from precursor phases. Garnet contains very high Re concentrations and may account for >50% of Re in some samples. The depletion of Pd in gabbroic eclogites appears linked, at least in part, to the loss of Ni-rich sulphide. Both basaltic and gabbroic oceanic crust have elevated Pt/Os ratios, but Pt/Re ratios are not sufficiently high to generate the coupled Os-186-Os-187 enrichments observed in some mantle melts, even without Pt loss from basaltic crust. However, the apparent mobility of Pt and Re in slab fluids provides an alternative mechanism for the generation of Pt- and Re-rich mantle material, recently proposed as a potential source of Os-187-Os-186 enrichment.
ISSN: 0016-7037

hal-00420072
https://hal.archives-ouvertes.fr/hal-00420072
DOI : 10.1016/j.gca.2008.11.036