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We describe a potentially new species of a platinum cupride–stannide mineral (PCSM) of composition Pt(Cu0.67Sn0.33). It occurs in a placer deposit in the River Bolshoy Khailyk, southern Krasnoyarskiy kray, Russia. A synthetic equivalent of PCSM was obtained and characterized. The PCSM occurs as anhedral or subhedral grains up to 15 μm × 30 μm in association with various platinum-group minerals, Rh–Co-rich pentlandite and magnetite, all hosted by a placer grain of Cu–Au–Pt alloy. Synchrotron micro-Laue diffraction studies indicate that the PCSM mineral is tetragonal and belongs to the inferred space-group P4/mmm (#123). Its unit-cell parameters are a = 2.838 (3) Å, c = 3.650 (4) Å, and V = 29.40 (10) Å3, and Z = 1. The c:a ratio calculated from the unit-cell parameters is 1.286. These characteristics are in good agreement with those obtained for specimens of synthetic Pt(Cu0.67Sn0.33). A review on related minerals and unnamed phases is provided to outline compositional variations and extents of solid solutions in the relevant systems PtNi–PtFe–PtCu, PdCu–PdHg–PdAu, PdHg–PtHg, and AuCu–PtCu. The PCSM-bearing mineralization appears to be related genetically with an ophiolitic source-rock of the Aktovrakskiy complex of the western Sayans. The unnamed phase likely crystallized from microvolumes of a highly fractionated melt rich in Cu and Sn.

For the first time, corona-type textures are described in ultrabasic rocks in three complexes of the Serpentinite Belt on the Kola Peninsula in the northeastern Fennoscandian Shield. Three variants of the corona texture formed at different stages during the crystallization of a komatiitic, Al-undepleted melt emplaced in a subvolcanic setting. The first type crystallized at an early stage (Mg# Ol = 87) in a fine-grained harzburgite of the Chapesvara-I sill, with the following order in the corona: Ol → Opx → Cpx → Pl → Amp (aluminous sodic-calcic). The second type displays the sequence Opx → Cpx → Amp → Pl → Qz, which is observed in the orthopyroxenite zone in the Lotmvara-I sill. The third type involves a symplectitic corona in a plagioclase-bearing orthopyroxenite in the Lyavaraka complex, in which the inferred order is: Cpx → Amp (aluminous hornblende) + symplectitic Qz, formed in direct contact with grains of Pl. The corona-type textures occur in fresh rocks and are not related to regional metamorphism. They likely formed as consequences of two important factors: (1) rapid cooling, leading to unsteady conditions of crystallization in a shallow setting; and (2) an intrinsic enrichment in H2O and other volatiles in the parental magma, giving rise to fluid-saturated environments at advanced stages of crystallization. This was followed by a deuteric deposition of Amp rims as a result of the accumulation of H2O and reaction of H2O-bearing fluid with early grains of pyroxene and late plagioclase. The likely existence of a close relationship is suggested by the drusites of the Belomorian complex, which are coeval. In addition, unusual occurrences of lamellar inclusions of phlogopite and Al2SiO5 are documented, hosted by interstitial grains of plagioclase in the orthopyroxenite zone of the Lotmvara-I sill. These are attributed to crystallization from late portions of remaining melt enriched in Al, K, Na, H2O, and Cl, which is indicated by the recorded occurrence of chlorapatite in this association. Thus, our findings indicate the presence and abundance of intrinsic volatiles, Cl, F, CO2, and especially magmatic H2O, which were important to lower the liquidus, decrease the density and viscosity of the highly magnesian melt of Al-undepleted komatiite, thus enabling its transport from the mantle to a shallow level in the crust.

Tamuraite, ideally Ir5Fe10S16, occurs as discrete phases (≤20 μm) in composite inclusions hosted by grains of osmium (≤0.5 mm across) rich in Ir, in association with other platinum-group minerals in the River Ko deposit of the Sisim Placer Zone, southern Krasnoyarskiy Kray, Russia. In droplet-like inclusions, tamuraite is typically intergrown with Rh-rich pentlandite and Ir-bearing members of the laurite–erlichmanite series (up to ~20 mol.% “IrS2”). Tamuraite is gray to brownish gray in reflected light. It is opaque, with a metallic luster. Its bireflectance is very weak to absent. It is nonpleochroic to slightly pleochroic (grayish to light brown tints). It appears to be very weakly anisotropic. The calculated density is 6.30 g·cm−3. The results of six WDS analyses are Ir 29.30 (27.75–30.68), Rh 9.57 (8.46–10.71), Pt 1.85 (1.43–2.10), Ru 0.05 (0.02–0.07), Os 0.06 (0.03–0.13), Fe 13.09 (12.38–13.74), Ni 12.18 (11.78–13.12), Cu 6.30 (6.06–6.56), Co 0.06 (0.04–0.07), S 27.23 (26.14–27.89), for a total of 99.69 wt %. This composition corresponds to (Ir2.87Rh1.75Pt0.18Ru0.01Os0.01)Σ4.82(Fe4.41Ni3.90Cu1.87Co0.02)Σ10.20S15.98, calculated based on a total of 31 atoms per formula unit. The general formula is (Ir,Rh)5(Fe,Ni,Cu)10S16. Results of synchrotron micro-Laue diffraction studies indicate that tamuraite is trigonal. Its probable space group is R–3m (#166), and the unit-cell parameters are a = 7.073(1) Å, c = 34.277(8) Å, V = 1485(1) Å3, and Z = 3. The c:a ratio is 4.8462. The strongest eight peaks in the X-ray diffraction pattern [d in Å(hkl)(I)] are: 3.0106(26)(100), 1.7699(40)(71), 1.7583(2016)(65), 2.7994(205)(56), 2.9963(1010)(50), 5.7740(10)(45), 3.0534(20)(43) and 2.4948(208)(38). The crystal structure is derivative of pentlandite and related to that of oberthürite and torryweiserite. Tamuraite crystallized from a residual melt enriched in S, Fe, Ni, Cu, and Rh, these elements were incompatible in the Os–Ir alloy that nucleated in lode zones of chromitites in the Lysanskiy layered complex, Eastern Sayans, Russia. The name honors Nobumichi Tamura, senior scientist at the Advanced Light Source of the Lawrence Berkeley National Laboratory, Berkeley, California.

We describe occurrences of platinum-group minerals (PGM) and an uncommon mineral enriched in Cl, and provide a brief review of Cl-bearing minerals associated with basic–ultrabasic complexes. An unusual phosphohedyphane-like phase (~30 µm), close to CaPb4(PO4)3Cl, occurs in one of the PGM-bearing veins of massive sulfides in the Monchepluton layered complex, Kola Peninsula, Russia. These veins consist of varying amounts of pyrrhotite, pentlandite, chalcopyrite, pyrite and accessory grains of galena; they are fairly abundant in the heavy-mineral concentrate, as are small (

Highly atypical mineralization involving Pd-Pt, Au-Ag, REE, Y, Zr, U, Th, and Cl-F-enriched minerals is found in zones with base metal sulfides (BMS, ~5 vol.% to 20 vol.%) in the eastern portion of the Oktyabrsky deposit in the Norilsk complex (Russia). The overall variations in Mg# index, 100 Mg/(Mg + Fe2+ + Mn), in host-rock minerals are 79.8 → 74.1 in olivine, 77.7 → 65.3 in orthopyroxene, 79.9 → 9.2 in clinopyroxene, and An79.0&nbsp, → An3.7. The span of clinopyroxene and plagioclase compositions reflects their protracted crystallization from early magmatic to late interstitial associations. The magnesian chromite (Mg# 43.9) trends towards Cr-bearing magnetite with progressive buildups in oxygen fugacity, ilmenite varies from early Mg-rich to late Mn-rich variants. The main BMS are chalcopyrite, pyrrhotite, troilite, and Co-bearing pentlandite, with less abundant cubanite (or isocubanite), rare bornite, Co-bearing pyrite, Cd-bearing sphalerite (or wurtzite), altaite, members of the galena-clausthalite series and nickeline. A full series of Au-Ag alloy compositions is found with minor hessite, acanthite and argentopentlandite. The uncommon assemblage includes monazite-(Ce), thorite-coffinite, thorianite, uraninite, zirconolite, baddeleyite, zircon, bastnäsite-(La), and an unnamed metamict Y-dominant zirconolite-related mineral. About 20 species of PGM (platinum group minerals) were analyzed, including Pd-Pt tellurides, bismuthotellurides, bismuthides and stannides, Pd antimonides and plumbides, a Pd-Ag telluride, a Pt arsenide, a Pd-Ni arsenide, and unnamed Pd stannide-arsenide, Pd germanide-arsenide and Pt-Cu arseno-oxysulfide. The atypical assemblages are associated with Cl-rich annite with up to 7.54 wt.% Cl, Cl-rich hastingsite with up 4.06 wt.% Cl, ferro-hornblende (2.53 wt.% Cl), chlorapatite (&gt, 6 wt.% Cl) and extensive solid solutions of chlorapatite, fluorapatite and hydroxylapatite, Cl-bearing members of the chlorite group (chamosite, up to 0.96 wt.% Cl), and a Cl-bearing serpentine (up to 0.79 wt.% Cl). A decoupling of Cl and F in the geochemically evolved system is evident. The complex assemblages formed late from Cl-enriched fluids under subsolidus conditions of crystallization following extensive magmatic differentiation in the ore-bearing sequences.

Dunite&ndash, harzburgite&ndash, olivine-bearing orthopyroxenite successions in the subvolcanic Chapesvara-I and Chapesvara-II intrusions in the Serpentinite Belt, western Kola Peninsula, are notably magnesian. The mean Mg# value (whole-rock) is 86.6, and the olivine is Fo84&minus, 89. The upper contact facies (UCF) displays a lower Mg# (81.6). It consists of grains of Fo92 and abundant chromian spinel, implying rapid crystallization of an almost unfractionated melt. On average, the whole-rock Al2O3/TiO2 value is 22.45, close to 22.9 (UCF) and to the primitive mantle, ~22. The rise of primitive ultramafic magma presumably occurred in a special tectonic setting at the boundary of the Paleoproterozoic Lapland Granulite Terrane and the Belomorian Composite Terrane of Archean age. The Chapesvara suite resembles examples of the Al-undepleted komatiites in the Barberton Belt, South Africa, with magmas of up to 30&ndash, 35% MgO. The UCF rock yields an anomalously low molar MgO/SiO2 value, close to that of dunitic rocks located at the center of the Chapesvara-II body. This rock is the most primitive, as indicated by the maximum Fo content of olivine, the lowest value of (Gd/Yb)N, 0.52, and the lowest abundances of middle to heavy rare-earth elements (REE) in the chondrite-normalized spectrum. The crystallization of the Chapesvara-II sill-like intrusion likely proceeded in two stages, which are evident from the olivine compositions varying from the maximum Fo92 (UCF) to Fo&le, 89.5 (the central dunite zone). At Stage 1, the UCF rock (Fo92) crystallized first, close to the upper contact. The area of crystallization then shifted to a central portion of the Chapesvara-II body, in which the dunitic zone (Fo89.5) formed in situ (Stage 2). The compositional variations in chromian spinel are consistent with this suggestion. Two crystallization trends were recognized. The type-1 trend displays a relative maximum or minimum close to the center, and then diverges into two linear subtrends directed upward and downward. This pattern is manifested in the variations of Mg# in olivine and chromian spinel, the whole-rock contents of Al and Ca, and in levels of incompatible elements: Ti, V, Zr, Y, and Hf. The type-2 trend decreases or increases uniformly from top to bottom. Variations in amount of Ni in olivine, the Fe3+# index in chromian spinel, and in values of Mg# (rocks), follow a type-2 trend. Variations in total amounts of REE, Nb, and Th, which gradually increase downward, are also related to a type-2 trend. Thus, a contrasting development and possible interference of the two types of evolutionary trends were observed in the crystallization history of the Chapesvara-II sill-like body. A double-front crystallization, hitherto unreported, involved two fronts moving upward and downward, respectively. The upward subtrend appeared to be of subordinate importance, whereas the extent of fractional crystallization of the downward front was much greater. Crystallization proceeded from the top to the bottom, presumably because of the preferential loss of heat at the roof. Variations in the Fe3+# index indicate that the level of fO2 also increased downward with progressive crystallization. Convection cells were presumably the key mechanism of accumulation of the crystallizing olivine grains to form the central dunite zone close to the center of the sill-like intrusion. The observed characteristics of the Chapesvara complex indicate the existence of a primitive-mantle source and imply a highly magnesian composition of intruding magma not only for Chapesvara, but also for the Pados-Tundra layered complex and associated suites of the Serpentinite Belt in the Kola Peninsula.

We describe assemblages of platinum-group minerals (PGM) and associated PGE&ndash, Au phases found in alluvium along the River Bolshoy Khailyk, in the western Sayans, Russia. The river drains the Aktovrakskiy ophiolitic complex, part of the Kurtushibinskiy belt, as does the Zolotaya River ~15 km away, the site of other placer deposits. Three groups of alloy minerals are described: (1) Os&ndash, Ir&ndash, Ru compositions, which predominate, (2) Pt&ndash, Fe compositions of a Pt3Fe stoichiometry, and (3) Pt&ndash, Au&ndash, Cu alloys, which likely crystallized in the sequence from Au&ndash, (Cu)-bearing platinum, Pt(Au,Cu), Pt(Cu,Au), and PtAuCu2, to PtAu4Cu5. The general trends of crystallization of PGM appear to be: [Os&ndash, Ru alloys] &rarr, Pt3Fe-type alloy (with inclusions of Ru-dominant alloy formed by exsolution or via replacement of the host Pt&ndash, Fe phase) &rarr, Pt&ndash, Cu alloys. We infer that Rh and Co mutually substitute for Fe, not Ni, and are incorporated into the pentlandite structure via a coupled mechanism of substitution: [Rh3+ + Co3+ + □ &rarr, 3Fe2+]. Many of the Os&ndash, Ru and Pt&ndash, Fe grains have porous, fractured or altered rims that contain secondary PGE sulfide, arsenide, sulfarsenide, sulfoantimonide, gold, Pt&ndash, Ni-rich alloys, and rarer phases like Cu-rich bowieite and a Se-rich sulfarsenide of Pt. The accompanying pyroxene, chromian spinel and serpentine are highly magnesian, consistent with a primitive ultramafic source-rock. Whereas the alloy phases indicate a highly reducing environment, late assemblages indicate an oxygenated local environment leading to Fe-bearing Ru&ndash, Os oxide (zoned) and seleniferous accessory phases.

The platinum-group minerals (PGM) consist of a group of accessory minerals that concentrate the six platinum-group elements (PGE): osmium (Os), iridium (Ir), ruthenium (Ru), rhodium (Rh), platinum (Pt), and palladium (Pd) [...]

Tetra-auricupride, ideally AuCu, represents the only species showing the coexistence of Au with an elevated level of Pt, as in the case of a detrital grain studied structurally for the first time, from an ophiolite-associated placer at Bolshoy Khailyk, western Sayans, Russia. We infer that tetra-auricupride can incorporate as much as ~30 mol. % of a &ldquo, PtCu&rdquo, component, apparently without significant modification of the unit cell. The unit-cell parameters of platiniferous tetra-auricupride are: a 2.790(1) &Aring, c 3.641(4) &Aring, with c/a = 1.305, which are close to those reported for ordered AuCu(I) in the system Au&ndash, Cu, and close also to the cell parameters of tetraferroplatinum (PtFe), which both appear to crystallize in the same space group, P4/mmm. These intermetallic compounds and natural alloys are thus isostructural. The closeness of their structures presumably allows Pt to replace Au atoms so readily. The high extent of Cu + Au enrichment is considered to be a reflection of geochemical evolution and buildup in levels of the incompatible Cu and Au with subordinate Pt in a remaining volume of melt at low levels of fO2 and fS2 in the system.

Compositional variations of major and minor elements were examined in Pt–Fe alloys from various geological settings and types of deposits, both lode and placer occurrences. They included representatives of layered intrusions, Alaskan-Uralian-(Aldan)-type and alkaline gabbroic complexes, ophiolitic chromitites, and numerous placers from Canada, USA, Russia, and other localities worldwide. Pt–Fe alloy grains in detrital occurrences are notably larger in size, and these are considered to be the result of a special conditions during crystallization such as temperature, pressure, geochemistry or time. In addition, the number of available statistical observations is much greater for the placer occurrences, since they represent the end-product of, in some cases, the weathering of many millions of tonnes of sparsely mineralized bedrock. Typically, platinum-group elements (PGE) present in admixtures (Ir, Rh, and Pd) and minor Cu, Ni are incorporated into a compositional series (Pt, PGE)2–3(Fe, Cu, Ni) in the lode occurrences. Relative Cu enrichment in alloys poor in Pt implies crystallization from relatively fractionated melts at a lower temperature. In contrast to the lode deposits, the distribution of Ir, Rh, and Pd is fairly chaotic in placer Pt–Fe grains. There is no relationship between levels of Ir, Rh, and Pd with the ratio Σ(Pt + PGE):(Fe + Cu + Ni). The compositional series (Pt, PGE)2–3(Fe, Cu, Ni) is not as common in the placer occurrences; nevertheless, minor Cu and Ni show their maximums in members of this series in the placer grains. Global-scale datasets yield a bimodal pattern of distribution in the Pt–Fe diagram, which is likely a reflection of the miscibility gap between the ordered Pt3Fe structure (isoferroplatinum) and the disordered structure of native or ferroan platinum. In the plot Pt versus Fe, there is a linear boundary due to ideal Pt ↔ Fe substitution. Two solid solution series are based on the Ir-for-Pt and Pd-for-Pt substitutions. The incorporation of Ir is not restricted to Pt3Fe–Ir3Fe substitution (isoferroplatinum and chengdeite, plus their disordered modifications). Besides, Ir0 appears to replace Pt0 in the disordered variants of (Pt–Ir)–Fe alloys. There is a good potential for the discovery of a new species with a Pd-dominant composition, (Pd, Pt)3Fe, most likely in association with the alkaline mafic-ultramafic or gabbroic complexes, or the mafic units of layered intrusions. The “field of complicated substitutions” is recognized as a likely reflection of the crystallochemical differences of Pd and Ir, extending along the Ir-Pd axis of the Ir–Pd–Rh diagram. The inferred solid solution extends approximately along the line Ir–(Pd:Rh = 2:3). Minor Pd presumably enters the solid solution via a coupled substitution in combination with the Rh. An Ir-enrichment trend in Pt–Fe alloys typically occurs in the Alaskan-type complexes. The large size of the Pt–Fe nuggets associated with some of these complexes is considered to be related to an ultramafic-mafic pegmatite facies, whereas significant Pd-enrichment is characteristic of gabbroic source-rocks (e.g., Coldwell Complex), resulting in a markedly different trend for the Pt versus Fe (wt.%). However, based on our examination of a large dataset of Pt–Fe alloys from numerous origins, we conclude that they exhibit compositional overlaps that are too large to be useful as reliable index-minerals.