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Oxygen-bearing platinum group minerals (O-bearing PGMs) are intergrown with base metal sulfides (BMS, e.g., pentlandite–[NiFe]9S8) within fractures in chromite grains from chromitite bodies on Ouen Island, New Caledonia. These PGMs are hosted in chlorite and serpentine, which formed during serpentinization of olivine and pyroxene. The O-bearing PGM grains are polygonal, show microfracturing (indicating volume loss), and contain Pt-Pd-rich sulfide remnants, suggesting pseudomorphic replacement of primary (magmatic) sulfides. They display chemical zonation, with Pt(-Pd-Ni-Fe) relict sulfide cores replaced by Pt-Fe-Ni oxidized alloy mantles and Pt-Cu-Fe(-Pd) alloy rims (tulameenite), indicating desulfurization. The core and mantle show a nanoporous structure, interpreted as the result of coupled dissolution–reprecipitation reactions between magmatic sulfides and low fO2–fS2 serpentinite-related fluids, probably formed during olivine transformation to serpentine + magnetite (early stages of serpentinization). This fluid infiltrated magmatic sulfides (PGE-rich and BMS), degrading them to secondary products and releasing S and metals that were accommodated in the mantle and rim of O-bearing PGMs. Upon olivine exhaustion, an increase in fO2 might have stabilized Pt-Fe-O compounds (likely Pt0/Pt-Fe + Fe oxyhydroxides) alongside Ni-Fe alloys. Our results show that post-magmatic desulfurization of primary sulfides produces complex nano-scale intergrowths, mainly driven by changes in the fluid's physicochemical properties during serpentinization. [ABSTRACT FROM AUTHOR]

We report the results of a mineralogical investigation of placer samples from the upper reaches of the Sisim watershed, near Krasnoyarsk, in Eastern Sayans, Russia. The placer grains are predominantly Os–Ir–(Ru) alloys (80%) that host various inclusions (i.e., platinum-group elements (PGE)-rich monosulfide, PGE-rich pentlandite, Ni–Fe–(As)-rich laurite, etc.) and subordinate amounts of Pt–Fe alloys. Analytical data (wavelength- and energy-dispersive X-ray spectroscopy) are presented for all the alloy minerals and the suite of micrometer-sized inclusions that they contain, as well as associated grains of chromian spinel. The assemblage was likely derived from chromitite units of the Lysanskiy mafic–ultramafic complex, noted for its Ti–(V) mineralization. In the Os–Ir–(Ru) alloys, the ratio Ru/Ir is ≤1, Ir largely substitutes for Os, and compositional variations indicate the scheme [Ir + Ru] → 2Os. In contrast, in the laurite–erlichmanite series, Ir and Os are strongly and positively correlated, whereas Ir and Ru are negatively correlated; Ru and Os are inversely correlated. These compositions point to the scheme [Os2+ + 2Ir3+ + □] → 4Ru2+ or alternatively, to Os2+ + Ir2+ → 2Ru2+. We deduce a potential sequence of crystallization in the parental rock and address the effects of decreasing temperature and increasing fugacity of sulfur and arsenic on the assemblage. Inclusions of Ti-rich minerals in the alloy grains are consistent with the Lysanskiy setting; the complete spectrum of chromite–magnesiochromite compositions indicates that an important part of that complex was eroded. A localized fluid-dominated micro-environment produced the unique association of laurite with monazite-(Ce), again considered a reflection of the special attributes of the Lysanskiy complex. [ABSTRACT FROM AUTHOR]