Chromitite zones associated with ultramafic units of the Lysanskiy layered complex of dunite–peridotite–gabbro composition could well represent the primary source for the placers bearing platinum-group minerals (PGM) of the entire drainage of the River Sisim and its tributaries, the rivers Ko and Seyba, eastern Sayans. Alluvial gold present in the placers of River Seyba, as elsewhere in the Sisim Placer Zone, reflects mineralisation during a recent period of tectonic activity. We focus on the PGM in the Seyba suite, and in particular on the attributes of pentlandite enriched in platinum-group-elements (PGE) and the compositionally similar and recently defined ferhodsite, which were trapped in host grains of Os–Ir–Ru alloy. Both minerals formed from small volumes of fractionated Fe–Ni–Cu melt considerably enriched in the PGE. In the Seyba suite, as in several others, the amounts of PGE in ferhodsite exceeds that in pentlandite, which results in a greater proportion of vacancies than in pentlandite.

Skaergaardite, PdCu, is a new mineral discovered in the Skaergaard intrusion, Kangerdlugssuaq area, East Greenland. It occurs in a tholeitiic gabbro associated with plagioclase, clinopyroxene, orthopyroxene, ilmenite, titanian magnetite, fayalite and accessory chlorite-group minerals, ferrosaponite, a member of the annite–phlogopite series, hornblende, actinolite, epidote, calcite, ankerite, apatite and baddeleyite. The mineral is found in composite microglobules composed of bornite, chalcocite, digenite, chalcopyrite, with rare cobalt pentlandite, cobaltoan pentlandite, sphalerite, keithconnite, vasilite, zvyagintsevite, (Cu,Pd,Au) and Pt-Fe-Cu-Pd alloys, unnamed PdCu3, (Pd,Cu,Sn), Au3Cu and PdAuCu. Skaergaardite occurs as droplets, equant grains with rounded outlines, subhedral to euhedral crystals and as irregular grains that vary in size from 2 to 75 μm, averaging 22 μm. It is steel grey with a bronze tint, has a black streak, a metallic lustre and is sectile. Neither cleavage nor fracture was observed. The mineral has a micro-indentation hardness of VHN25 = 257. It is isotropic, non-pleochroic and exhibits neither discernible internal reflections nor evidence of twinning. Skaergaardite varies from bright creamy white (associated with bornite and chalcopyrite) to bright white (associated with digenite and chalcocite). Reflectance values in air (and in oil) are: 58.65 (47.4) at 470 nm, 62.6 (51.1) at 546 nm, 64.1 (52.8) at 589 nm and 65.25 (53.95) at 650 nm. The average of 311 electron-microprobe analyses gives: Pd 58.94, Pt 1.12, Au 2.23, Cu 29.84, Fe 3.85, Zn 1.46, Sn 1.08, Te 0.28 and Pb 0.39, total 99.19 wt.%, corresponding to (Pd0.967Au0.020Pt0.010)Σ0.997(Cu0.820Fe0.120 Zn0.039Sn0.016Te0.004Pb0.003)Σ1.002. The mineral is cubic, space group Pm3m, a = 3.0014(2) Å, V = 27.0378 Å3, Z = 1. Dcalc is 10.64 g/cm3. The six strongest lines in the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.122(100)(110), 1.5000(20)(200), 1.2254(50)(211), 0.9491(20)(310), 0.8666(10)(222), 0.8021(70)(321). The mineral has the CsCl-type structure. It is believed to be isostructural with wairauite (CoFe), synthetic CuZn (β-brass) and is structurally related to hongshiite (PtCu). Skaergaardite developed from a disordered Pd-Cu-rich metal alloy melt that had exsolved from an earlier Cu-(Fe) sulphide melt. Ordering of Pd and Cu (beginning at T ≈ 600°C) results in development of the CsCl structure from a disordered face-centred cubic structure.

Gold of magmatic origin has been discovered in the lamproitic dyke of El Tale (Fortuna, Province of Murcia), a small outcrop of ultrapotassic rocks of tile Tertiary magmatic province of southeastern Spain. It is the first finding of gold grains in lamproite magmas from southeastern Spain, and indeed worldwide. Pure gold occurs only in the glassy groundmass as very rare spherules and globular grains (up to 5 µm). Despite the occurrence of gold grains, the bulk rock contains not more than ∼19 ppb Au.

The magmatic origin of gold is inferred from the heterogeneous distribution of the grains in the rock, the shape of the grains (which is comparable to that of gold grains crystallized experimentally from mafic liquids) and from the As-Sb-S-Cl-poor composition of the bulk rock. The Pd/Ir and Au/Pd ratios, little affected by the early segregation of olivine (∼10 vol.%), support an Au- and PGE-rich composition of the mantle source. The low f O2 (≈IW) and the complexing with F and alkalies probably favoured partitioning of Au and PGE into the lamproite magma.

Naldrettite, Pd2Sb, is a new intermetallic mineral discovered in the Mesamax Northwest deposit, Cape Smith fold belt, Ungava region, northern Québec. It is associated with monoclinic pyrrhotite, pentlandite, chalcopyrite, galena, sphalerite, cobaltite, clinochlore, magnetite, sudburyite (PdSb), electrum and altaite. Other rarer associated minerals include a second new mineral (ungavaite, Pd4Sb3), sperrylite (PtAs2), michenerite (PdBiTe), petzite (Ag3AuTe4) and hessite (Ag2Te). Naldrettite occurs as anhedral grains, which are commonly attached or moulded to sulphide minerals, and also associated with clinochlore. Grains of naldrettite vary in size (equivalent circle diameter) from ~10 to 239 μm, with an average of 74.4 mm (n = 632). Cleavage was not observed and fracture is irregular. The mineral has a mean micro-indentation hardness of 393 kg/mm2. It is distinctly anisotropic, non-pleochroic, has weak bireflectance, and does not exhibit discernible internal reflections. Some grains display evidence of strain-induced polysynthetic twinning. Naldrettite appears bright creamy white in association with pentlandite, pyrrhotite, clinochlore and chalcopyrite. Reflectance values in air (and in oil) for R1 and R2 are: 49.0, 50.9 (35.9, 37.6) at 470 nm, 53.2, 55.1 (40.3, 42.1) at 546 nm, 55.4, 57.5 (42.5, 44.3) at 589 nm and 58.5, 60.1 (45.4, 47.2) at 650 nm. The average of 69 electron-microprobe analyses on 19 particles gives: Pd 63.49, Fe 0.11, Sb 35.75, As 0.31, and S 0.02, total 99.68 wt.%, corresponding to (Pd1.995Fe0.007)2.002(Sb0.982AS0.014S0.002)0.998. The mineral is orthorhombic, space group Cmc21, a 3.3906(1), b 17.5551(5), c 6.957(2) Å , V 414.097(3) Å3, Z = 8. Dcalc is 10.694(1) g/cm3. The six strongest lines in the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.2454(100)(132), 2.0567(52)(043), 2.0009(40)(152), 1.2842(42)(115), 1.2122(50)(204) and 0.8584(56)(1.17.4).

Small (<2 km diameter), ultramafic intrusive complexes in the Andriamena region of Madagascar contain zones with disseminated chromite and sulphides which carry high concentrations of platinum-group elements (PGE). Assay of drill core from one complex, designated UM2, revealed three zones showing consistently high PGE grades. Mineralogical investigation of the UM2 core reveals that a small number of low reflecting, Pd-bearing platinum-group minerals (PGM) are present — always in association with a poorly characterized Pd stibio-arsenide [Pd3(Sb,As)] phase — in the shallowest of the three zones. Electron microprobe analysis of these PGM indicates the presence of oxygen and that at least two species exist. The resulting stoichiometries suggest that at least one species could be a hydrated form of palladinite [PdO.(H2O)n]. The other phase could be a hydroxide [Pd(OH)2] or a less strongly hydrated form of palladinite. Textural evidence suggests that the Pd-O species formed via the replacement of a precursor Pd-rich PGM, with only a limited removal of Pd, rather than via precipitation of a Pd-O PGM from a fluid that was Pd-bearing. The limited thermal stability of hydrated Pd oxides and the apparent restriction of the Pd-O phases to a shallow zone which is affected by the seasonal movement of groundwater, suggests that they may have formed at low temperatures via the leaching and replacement of other elements from a precursor Pd-rich PGM by oxygen and water during alternating water-saturated and dry conditions. If this is the case, the water table interface might be another environment, in addition to the surface, in which to look for the development of PGE oxides.

The system Pd-Fe-Ni-S was studied at 900 and 725°C by means of dry condensed charges. At both temperatures it is dominated by the phase relationships involving sulphide melt. Pd-Fe-Ni alloys with broad miscibility primarily coexist with the melt; they are relatively enriched in Pd, whereas the associated melt is enriched in Ni. With decreasing temperature the melt recedes from Fe-rich regions. The incompatibility of PdS (extensive solid solution with Ni) and mss at 900°C is replaced by their co-crystallization (± disulphide(s) of Ni,Fe or ± sulphide melt) at 725°C The Ni/Fe ratio in the melt changes regularly against that in mss with increasing S fugacity and Pd contents in these two phases. (Ni,Fe)3±xS2 and Pd4S play important roles at 725°C. The data offer an array of distribution coefficients and solubility values suitable for geological interpretations.

Highly anomalous platinum-group element (PGE) concentrations in the podiform chromitites at the Cliff and Harold's Grave localities in the Shetland ophiolite complex have been well documented previously. The focus of this study is alluvial platinum-group minerals (PGM) located in small streams that drain from the PGE-rich chromitites. The placer PGM assemblage at Cliff is dominated by Pt-arsenides (64%) and Pd-antimonides (17%), with less irarsite–hollingworthite (11%) and minor Pd-sulfides, Pt–Pd–Cu and Pt–Fe alloys and laurite. Gold also occurs with the PGM. Alluvial PGM have average sizes of 20 µm × 60 µm, with sperrylite the largest grain identified at 110 µm in diameter, matching the range reported for the primary PGM in the source rocks. The placer assemblage contains more Pt-bearing and less Pd-bearing PGM compared with the rocks. The more resistant sperrylite and irarsite–hollingworthite grains which are often euhedral become more rounded further downstream whereas the less resistant Pd-antimonides which are commonly subhedral may become striated and etched. Less stable phases such as Pt- and Pd-oxides and other Ni-Cu-bearing phases located in the rocks (i.e. Ru-pentlandite, PtCu, Pd–Cu alloy) are absent in the placer assemblage. Also the scarce PGM (PdHg, Rh- and Ir-Sb) and Os in the rocks are absent. At Harold's Grave only three alluvial PGM (laurite, Ir, Os) and Au were recovered reflecting the limited release of IPGM from chromite grains in the rocks. In this cold climate with high rainfall, where erosion dominates over weathering, the PGM appear to have been derived directly from the erosion of the adjacent PGE-rich source rocks and there is little evidence of in situ growth of any newly formed PGM. Only the presence of dendritic pure Au and Pd-, Cu-bearing Au covers on the surface of primary minerals may indicate some local reprecipitation of these metals in the surficial conditions.

The Conakry Igneous Complex is a mafic-ultramafic intrusion emplaced contemporaneously with the opening of the Atlantic, forming a complex, 55 km x 5 km dyke-like body within which three main episodes of injection have been recognized, characterized by a lack of mineral layering. Unit 1 consists of dunite and related facies, Unit 2 of wehrlite and pyroxene peridotite and Unit 3 corresponds to various gabbro facies. Units 1 and 2 constitute the Kaloum Peninsula; Unit 3 is its NW extension, forming the 1010 m high Mount Kakoulima. Unit 3 intrudes the two previous units and corresponds to a tholeiitic liquid that crystallized in an almost closed system, and thus exhibits a strong differentiation trend, in contrast to Units 1 and 2. Mineral compositions suggest the existence of a deeper magma chamber where a first stage of differentiation occurred.

Disseminated base-metal sulfides (BMS) are present in all units of the complex and earlier descriptions have mentioned a “massive sulfide layer” with 2 to 4 g/t PGE. Platinum-group minerals (PGM) are almost everywhere included in or attached to composite Ni–Fe–Cu sulfides. Most PGM grains form complex associations resulting either from exsolution or alteration. It is characteristic of the Conakry Igneous Complex PGM, described here for the first time, to be dominated by (Pd,Pt)(Te,Bi) minerals with rare Pd,Sn and Pd,Pb compositions and an absence of Pt,Pd sulfides and Pt,Pd antimonides.

The constant association of the PGM with the BMS shows that the magmatic sulfide liquid acts as an efficient collector of PGE. In such a dynamic environment, the process leading to the formation of massive sulfides must be sought in the accumulation of sulfides in the conduit following host-rock assimilation. Accordingly, considering the multiple injection processes that characterize the whole intrusion, the potential for discovering additional Ni–Cu–PGE mineralization in the Conakry Igneous Complex remains high.

The ~492 Ma Shetland Ophiolite Complex contains an extensive mantle section, within which numerous podiform chromitite bodies formed during melt percolation in a supra-subduction zone setting. One of the Shetland ophiolite chromitite localities has an unusual style of platinum-group element (PGE) mineralization. Specifically, the Cliff chromitite suite has relatively high (>250 ppm) Pt plus Pd, compared to other chromitites in the Shetland Ophiolite Complex. In this study, we apply petrographic observation, mineral chemistry and novel X-ray microtomography data to elucidate the petrogenesis of PGE-bearing phases at Cliff. The combined datasets reveal that the PGE at Cliff have probably been fractionated by an As-rich fluid, concentrating Pt and Ir into visible (0.1–1 µm) platinum-group minerals (PGM) such as sperrylite and irarsite, respectively. The high (>1 ppm) bulk-rock concentrations of the other PGE (e.g. Os) in the Cliff chromitites suggests the presence of abundant fine-grained unidentified PGM in the serpentinized groundmass. The spatial association of arsenide phases and PGM with alteration rims on Cr-spinel grains suggests that the high Pt and Pd abundances at Cliff result from a late-stage low-temperature (e.g. 200–300°C) hydrothermal event. This conclusion highlights the potential effects that secondary alteration processes can have on modifying and upgrading the tenor of PGE deposits.

The Waterberg platinum deposit is an extraordinary example of a vein-type hydrothermal quartz-hematite-PGE (platinum-group element) mineralization. This study concentrates on the geochemical character of the ores and the platinum-group mineral (PGM) assemblage by application of reflected-light and scanning electron microscopy followed by electron probe microanalysis.

The PGM-bearing quartz veins show multiple banding indicating numerous pulses of fluid infiltration. Mineralization was introduced contemporaneously with the earliest generation of vein quartz and hematite. High oxygen and low sulfur fugacities of the mineralizing fluids are indicated by hematite as the predominant opaque mineral and the lack of sulfides.

The ‘Waterberg type’ mineralization is characterized by unique metal proportions, namely Pt>Pd>Au, interpreted as a fingerprint to the cradle of the metals, namely rocks and ores of the Bushveld Complex, or reflecting metal fractionation during ascent of an oxidized, evolving fluid. The PGM assemblage signifies three main depositional and alteration events. (1) Deposition of native Pt and Pt–Pd alloys (>90% of the PGM assemblage) and Pd–Sb–As compounds (Pt-rich isomertieite and mertieite II) from hydrothermal fluids. (2) Hydrothermal alteration of Pt by Cu-rich fluids and formation of Pt–Cu alloys and hongshiite [PtCu]. (3) Weathering/oxidation of the ores producing Pd/Pt-oxides/hydroxides.

Platinum-group element transport was probably by chloride complexes in moderately acidic and strongly oxidizing fluids of relatively low salinity, and depositional temperatures were in the range 400–200°C. Alternatively, quartz and ore textures may hint to noble metal transport in a colloidal form and deposition as gels.

The source of the PGE is probably in platiniferous rocks or ores of the Bushveld Complex which were leached by hydrothermal solutions. If so, further Waterberg-type deposits may be present, and a prime target area would be along the corridor of the Thabazimbi-Murchison-Lineament where geothermal springs are presently still active.

Microcrystals of platinum-group element (PGE)-bearing cobaltite occur in the Gulcari A deposit of vanadiferous titanomagnetite in the lower zone of the Rio Jacaré mafic-ultramafic layered intrusion, Brazil. Aggregates of cobaltite and sperrylite are cluster-like and developed generally along the boundary of Fe-Ti oxide grains with deuteric silicates. Our observations of cryptic zoning, compositional variability and interelement correlations are based on 37 analytical points (wavelength-dispersion spectrometry mode) of cobaltite, and indicate that Ir and Rh behave uniformly with Ni and antipathetically with Co which, in turn, correlates directly with S content. Iridium, Rh and Ni apparently substitute for Co in the As-enriched grain core, and the substitution mechanism invokes solid solution with a cattierite-type molecule: (Ni + Ir + Rh) + (AsS) = Co + (S2). The PGE-bearing cobaltite probably crystallized as a primary phase at 500 to 300°C, from microvolumes of a late fluid phase. The observed enrichment in S and decrease in the As:S ratio at the cobaltite grain margins is a reflection of the increase in sulfur fugacity (fS2) with decrease in temperature of crystallization.

Palladosilicide, Pd2Si, is a new mineral (IMA 2014-080) discovered in chromite-rich samples from the Kapalagulu intrusion, western Tanzania (30°03′51′′E 5°53′16′′S and 30°05′37′′E 5°54′26′′S) and from the UG-2 chromitite, Bushveld complex, South Africa. A total of 13 grains of palladosilicide, ranging in size from 0.7 to 39.1 μm (equivalent circle diameters), were found. Synthetic Pd2Si is hexagonal, space group P62m, with a = 6.496(5), c = 3.433(4) Å, V = 125.5(1) Å3, c:a = 0.529 with Z = 3. The strongest lines calculated from the powder pattern (Anderko and Schubert, 1953) are [d in Å (I) (hkl)] 2.3658 100 (111); 2.1263 37 (120); 2.1808 34 (021); 3.240 20 (110); 1.8752 19 (030); 1.7265 12 (002); 1.3403 11 (122); 1.2089 10 (231). The calculated density for three analyses varies from 9.562 to 9.753 g cm–3. Palladosilicide is considered to be equivalent to synthetic Pd2Si based on results from electron backscattered diffraction analyses. Reflectance data in air for the four Commission on Ore Mineralogy wavelengths are [λ nm, R1 (%) R2 (%)] 470 49.6 52.7; 546 51.2 53.8; 589 51.6 53.7; 650 51.7 53.3 and the mineral is bright creamy white against chromite, weakly bireflectant and displays no discernible pleochroism or twinning. It is weakly anisotropic, has weak extinction and rotation tints in shades of blue and olive green. Electron probe microanalyses of palladosilicide yield a simplified formula of Pd2Si.

New Pd-Tl-(Bi,As)-rich compounds are described from the Anomal'nyi Cu-PGE deposit, Kondyor alkaline ultramafic complex, northeastern Russia. They occur in vein-type settings associated with bodies of 'kosvite' (magnetite-rich clinopyroxenite) in the dunite-(peridotite) core, in pegmatiticand micaceous rocks. The ore zones are substantially enriched in phlogopite; they consist of diopside, disseminated titaniferous magnetite and fluorapatite (Sr-bearing). The observed assemblages of ore minerals include sulfides of the chalcopyrite-bornite-(secondary chalcocite) associationand various species of platinum-group minerals (PGM) [isomertieite or arsenopalladinite rich in Sb, mertieite-II, mertieite-I, sobolevskite, kotulskite, merenskyite, zvyagintsevite, palarstanide, paolovite, sperrylite, maslovite or moncheite, hollingworthite and unnamed species of PGM] anda Ag-Au alloy. The oxides [Pd4(Bi,Te,Tl)O6 and Pd4(Tl,Bi,Te)O6] probably formed in situ by oxidation reactions at the expense of the associated PGM intergrowths. These involve palladium bismuthide-thallide phases, Pd5(Tl,As,Bi)and Pd5(As,Tl,Bi), which are documented here for the first time. A fairly evolved environment, enriched in Cu, Pd, Te, Bi, Pb and volatile components, is indicated for the vein-type deposit at Anomal'nyi.

Identification and accurate characterization of platinum-group minerals (PGMs) is usually a very cumbersome procedure due to their small grain size (typically below 10 µm) and inconspicuous appearance under reflected light. A novel strategy for finding PGMs and quantifying their composition was developed. It combines a mineral liberation analyzer (MLA), a point logging system, and electron probe microanalysis (EPMA).

As a first step, the PGMs are identified using the MLA. Grains identified as PGMs are then marked and coordinates recorded and transferred to the EPMA. Case studies illustrate that the combination of MLA, point logging, and EPMA results in the identification of a significantly higher number of PGM grains than reflected light microscopy. Analysis of PGMs by EPMA requires considerable effort due to the often significant overlaps between the X-ray spectra of almost all platinum-group and associated elements. X-ray lines suitable for quantitative analysis need to be carefully selected. As peak overlaps cannot be avoided completely, an offline overlap correction based on weight proportions has been developed. Results obtained with the procedure proposed in this study attain acceptable totals and atomic proportions, indicating that the applied corrections are appropriate.