Age of the Eastern Kaapvaal mantle: Re-Os isotope data for peridotite xenoliths from the Monastery kimberlite

2004 ◽  
Vol 107 (1-2) ◽  
pp. 81-90 ◽  
Author(s):  
R. W. Carlson
Author(s):  
Wolf Uwe Reimold ◽  
Toni Schulz ◽  
Stephan König ◽  
Christian Koeberl ◽  
Natalia Hauser ◽  
...  

ABSTRACT This contribution is concerned with the debated origin of the impact melt rock in the central uplift of the world’s largest confirmed impact structure—Vredefort (South Africa). New major- and trace-element abundances, including those of selected highly siderophile elements (HSEs), Re-Os isotope data, as well as the first Se isotope and Se-Te elemental systematics are presented for the felsic and mafic varieties of Vredefort impact melt rock known as “Vredefort Granophyre.” In addition to the long-recognized “normal” (i.e., felsic, >66 wt% SiO2) granophyre variety, a more mafic (<66 wt% SiO2) impact melt variety from Vredefort has been discussed for several years. The hypothesis that the mafic granophyre was formed from felsic granophyre through admixture (assimilation) of a mafic country rock component that then was melted and assimilated into the superheated impact melt has been pursued here by analysis of the two granophyre varieties, of the Dominion Group lava (actually metalava), and of epidiorite mafic country rock types. Chemical compositions, including high-precision isotope dilution–derived concentrations of selected highly siderophile elements (Re, Os, Ir, Pt, Se, Te), and Re-Os and Se isotope data support this hypothesis. A first-order estimate, based on these data, suggests that some mafic granophyre may have resulted from a significant admixture (assimilation) of epidiorite to felsic granophyre. This is in accordance with the findings of an earlier investigation using conventional isotope (Sr-Nd-Pb) data. Moreover, these outcomes are in contrast to a two-stage emplacement model for Vredefort Granophyre, whereby a mafic phase of impact melt, derived by differentiation of a crater-filling impact melt sheet, would have been emplaced into earlier-deposited felsic granophyre. Instead, all chemical and isotopic evidence so far favors formation of mafic granophyre by local assimilation of mafic country rock—most likely epidiorite—by a single intrusive impact melt phase, which is represented by the regionally homogeneous felsic granophyre.


Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 329
Author(s):  
Kreshimir N. Malitch ◽  
Inna Yu. Badanina ◽  
Elena A. Belousova ◽  
Valery V. Murzin ◽  
Tatiana A. Velivetskaya

This study presents new compositional and S-Os isotope data for primary Ru-Os sulfides within a platinum-group mineral (PGM) assemblage from placer deposits associated with the Verkh-Neivinsk massif, which is part of the mantle ophiolite association of Middle Urals (Russia). The primary nature of Ru-Os sulfides represented by laurite (RuS2)–erlichmanite (OsS2) series is supported by occurrence of euhedral inclusions of high-Mg olivine (Fo92–94) that fall within the compositional range of mantle (primitive) olivine (Fo 88–93). The sulfur isotope signatures of Ru-Os sulfides reveal a range of δ34S values from 0.3 to 3.3‰, with a mean of 2.05‰ and a standard deviation of 0.86‰ (n = 18), implying that the sulfur derived from a subchondritic source. A range of sub-chondritic initial 187Os/188Os values defined for Ru-Os sulfides (0.1173–0.1278) are clearly indicative of derivation from a sub-chondritic source. Re-depletion (TRD) ages of the Verkh-Neivinsk Ru-Os sulfides are consistent with prolonged melt-extraction processes and likely multi-stage evolution of highly siderophile elements (HSE) within the upper mantle. A single radiogenic 187Os/188Os value of 0.13459 ± 0.00002 determined in the erlichmanite is indicative of a supra-chondritic source of HSE. This feature can be interpreted as evidence of a radiogenic crustal component associated with a subduction event or as an indication of an enriched mantle source. The mineralogical and Os-isotope data point to a high-temperature origin of the studied PGM and two contrasting sources for HSE in Ru-Os sulfides of the Verkh-Neivinsk massif.


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