Distribution of platinum-group elements in magmatic and altered ores in the Jinchuan intrusion, China: an example of selenium remobilization by postmagmatic fluids

The division of platinum-group elements (PGE) between those hosted in platinum-group minerals (PGM) versus those in solid solution in base metal sulfides (BMS) has been determined for ores from the PGE-bearing Ni-Cu-rich Jinchuan intrusion in northwest China. All the BMS are devoid of Pt and Ir, and magmatic BMS are also barren of Rh. These PGE may have been scavenged by arsenic to form PGM during magmatic crystallization of the BMS. Pd, Os, and Ru are recorded in BMS and Pd is predominantly in solid solution in pentlandite. Unlike the fresh magmatic ores, in altered or serpentinized ores, Pd-PGM are present. Froodite is hosted in magnetite, formed during alteration of BMS, accompanied by sulfur loss and liberation of Pd. Michenerite ([Pd,Pt]BiTe), sperrylite (PtAs₂), and Au-bearing PGM are located in altered silicates. Irarsite (IrAsS) occurs mainly enclosed in BMS. Padmaite (PdBiSe), identified at the junctions of magnetite and BMS, was the last PGM to form and locally partially replaces earlier non-Se-bearing PGM. We propose that padmaite formed under oxidizing conditions during late local remobilization of Se from the BMS. Se-bearing PGM are rare and our review shows they are frequently associated with carbonate, suggesting that Pd and Se can be mobilized great distances in low pH oxidizing fluids and may be precipitated on contact with carbonate. S/Se ratios are used by researchers of magmatic Ni-Cu-PGE ores to determine sulfur loss, assuming Se is immobile and representative of magmatic sulfur content. This study shows that Se as well as S is potentially mobile and this should be considered in the use of S/Se ratios.     

The mineralogy and mineral associations of platinum group elements and gold in the Platreef at Zwartfontein, Akanani Project, Northern Bushveld Complex, South Africa

The mineralogy of the platinum-group elements (PGE), and gold, in the Platreef of the Bushveld Complex, was investigated using an FEI Mineral Liberation Analyser. Polished sections were prepared from 171 samples collected from two boreholes, for the in-situ examination of platinum group minerals (PGM). PGM and gold minerals encountered include maslovite (PtBiTe, 32 area% of total PGM), kotulskite (Pd(BiTe), 17?%), isoferroplatinum (Pt₃Fe, 15?%), sperrylite (PtAs₂, 11?%), cooperite (PtS, 5?%), moncheite (PtTe₂; 5?%), electrum (AuAg; 5?%), michenerite (PdBiTe; 3?%), Pd alloys (Pd, Sb, Sn; 3?%), hollingworthite ((Rh,Pt)AsS; 2?%), as well as minor (all <1 area% of total PGM) merenskyite (PdBiTe₂), laurite (RuS₂), rustenburgite (Pt_0.4Pd_0.4Sn_0.2), froodite (PdBi₂), atokite (Pd_0.5Pt_0.3Sn_0.2), stumpflite (PtSb), plumbopalladinite (Pd₃Pb₂), and zvyagintsevite (Pd₃Pb). An observed association of all PGM with base metal sulfides (BMS), and a pronounced association of PGE tellurides, arsenides and Pd&Pt alloys with secondary silicates, is consistent with the remobilisation and recrystallisation of some of the PGM’s during hydrothermal alteration and serpentinisation subsequent to their initial (primary) crystallisation from BMS (e.g. Godel et al. J Petrol 48:1569–1604, 2007; Hutchinson and McDonald Appl Earth Sci (Trans Inst Min Metall B) 114:B208–224, 2008).     

Palladium and gold mineralization in podiform chromitite at Kraubath, Austria

Summary ?We report, for the first time, the occurrence of five palladium-rich, one palladium bearing and two gold-silver minerals from podiform chromitites in the Eastern Alps. Minerals identified include braggite, keithconnite, stibiopalladinite, potarite, mertieite II, Pd-bearing Pt-Fe alloy, native gold and Ag-Au alloy. They occur in heavy mineral concentrates produced from two massive podiform chromitite samples (unaltered and highly altered) of the Kraubath ultramafic massif, Styria, Austria. Distribution patterns of platinum-group elements (PGE) in these chromitites show considerable differences in the behaviour of the less refractory PGE (PPGE-group: Rh, Pt, Pd) compared to the refractory PGE (IPGE-group: Os, Ir, Ru). PPGE are more enriched in chromitite showing pronounced alteration features. The unaltered chromitite displays a negatively sloped chondrite-normalised PGE pattern similar to typical ophiolitic-podiform chromitite. Except for the Pd- and Au-Ag minerals that are generally rare in ophiolites, about 20 other platinum-group minerals (PGM) have been discovered. They include PGE-sulphides (laurite, erlichmanite, kashinite, bowieite, cuproiridsite, cuprorhodsite, unnamed Ir-rich variety of ferrorhodsite, unnamed Ni-Fe-Cu-Rh- and Ni-Fe-Cu-Ir-Rh monosulphides), PGE alloys (Pt-Fe, Ir-Os, Os-Ir and Ru-Os-Ir), PGE-sulpharsenides (irarsite, hollingworthite, platarsite, ruarsite and a number of intermediate species), sperrylite and a Ru-rich oxide (?). Three PGM assemblages have been recognised and attributed to different processes ranging from magmatic to hydrothermal and weathering-related. Pd-rich minerals are characteristic of both chromitite types, although their chemistry and relative proportions vary considerably. Keithconnite, braggite and Pd-bearing ferroan platinum, together with a number of PGE-sulphides (mainly laurite-erlichmanite) and alloys, are typical only of the unaltered podiform chromitite (assemblage I). Euhedral mono- and polyphase PGM grains in the submicron to 100 μm range show features of primary magmatic assemblages. The diversity of PGM in these assemblages is unusual for ophiolitic environments. In assemblage II, laurite-erlichmanite is intergrown with and overgrown by PGE-sulpharsenides; other minerals of assemblage I are missing. Potarite, stibiopalladinite, mertieite II, native gold and Ag-Au alloys, as well as PGE-sulpharsenides, sperrylite and base metal arsenides and sulphides are characteristic for the highly altered chromitite (assemblage III). They occur either interstitial to chromite in association with metamorphic silicates, in chromite rims or along cracks, and are thus interpreted as having formed by remobilization of PGE by hydrothermal processes during polyphase regional metamorphism. Received August 3, 2000;/revised version accepted December 28, 2000     

铂族元素矿物共生组合(英文)

由于铂族元素能有效地降低汽车尾气的污染 ,其需求量日益增加 ,对铂族元素矿床的寻找已是当务之急。着重从矿物矿床学角度对铂族元素的矿物共生特点进行了探讨。铂族元素可呈独立矿床产出 ,主要产于基性超基性层状侵入体、蛇绿岩套及阿拉斯加式侵入体中。铂族元素也伴生于铜镍矿床中 ,该类铜镍矿床主要与苏长岩侵入体、溢流玄武岩及科马提岩有关。产于基性超基性层状侵入体中的铂族矿物有铂钯硫化物、铂铁合金、钌硫化物、铑硫化物、铂钯碲化物、钯砷化物及钯的合金。这些铂族矿物可与硫化物矿物共生 ,也可与硅酸盐矿物共生 ,还可与铬铁矿及其他氧化物矿物共生。产于蛇绿岩套中的铂族矿物主要是钌铱锇的矿物 ,而铂钯铑的矿物则较少出现 ,这些铂族矿物可呈合金、硫化物、硫砷化物以及砷化物 4种形式出现。产于阿拉斯加式侵入体中的铂族矿物主要有铂铁合金、锑铂矿、硫铂矿、砷铂矿、硫锇矿及马兰矿等少数几种 ,其中铂铁合金与铬铁矿及与其同时结晶的高温硅酸盐矿物共生 ,而其他的铂族矿物则与后来的变质作用及蛇纹岩化作用中形成的多金属硫化物及砷化物共生。产于铜镍矿床中的铂族矿物主要是铂和钯的矿物。产于基性超基性层状侵入体、蛇绿岩套及阿拉斯加式侵入体中的铂族矿物的共同特点是它们均与铬铁矿?     

Diversity of platinum-group mineral assemblages in banded and podiform chromitite from the Kraubath ultramafic massif,Austria: evidence for an ophiolitic transition zone?

We report highly unusual platinum-group mineral (PGM) assemblages from geologically distinct chromitites (banded and podiform) of the Kraubath massif, the largest dismembered mantle relict in the Eastern Alps. The banded chromitite has a pronounced enrichment of Pt and Pd relative to the more refractory platinum-group elements (PGEs) of the IPGE group (Os, Ir, Ru), similar to crustal sections of ophiolites. On the contrary, the podiform chromitite displays a negatively sloping chondrite-normalised PGE pattern typical of ophiolitic podiform chromitite. The chemical composition of chromite varies from Cr# 73-77 in the banded type to 81-86 in the podiform chromitite. Thirteen different PGMs and one gold-rich mineral are first observed in the banded chromitite. The dominant PGM is sperrylite (53% of all PGMs), which occurs in polyphase assemblages with an unnamed Pt-base metal (BM) alloy and Pd-rich minerals such as stibiopalladinite, mayakite, mertieite II, unnamed Pd-Rh-As and Pd(Pt)-(As,Sb) minerals. This banded type also contains PGE sulphides (about 7%) represented by a wide compositional range of the laurite-erlichmanite series and irarsite (8%). Os-Ir alloy, geversite, an unnamed Pt-Pd-Bi-Cu phase and tetrauricupride are present in minor amounts. By contrast, the podiform chromitite, which yielded 21 different PGMs, is dominated by laurite (43% of all PGMs) which occurs in complex polyphase assemblages with PGE alloys (Ir-Os, Os-Ir, Pt-Fe), PGE sulphides (kashinite, bowieite, cuproiridsite, cuprorhodsite, unnamed (Fe,Cu)(Ir,Rh)₂S₄, braggite, unnamed BM-Ir and BM-Rh sulphides) and Pd telluride (keithconnite). A variety of PGE sulpharsenides (33%) including irarsite, hollingworthite, platarsite, ruarsite and a number of intermediate species have been identified, whereas sperrylite and stibiopalladinite are subordinate (2%). The occurrence of such a wide variety of PGMs from only two, 2.5-kg chromitite samples is highly unusual for an ophiolitic environment. Our novel sample treatment allowed to identify primary PGM assemblages containing all six PGEs in both laurite-dominated podiform chromitite as well as in uncommon sperrylite-dominated banded chromitite. We suggest that the geologically, geochemically and mineralogically distinct banded chromitite from Kraubath characterises the transition zone of an ophiolite, closely above the mantle section hosting podiform chromitite, rather than being representative of the crustal cumulate pile.     

Textural,mineralogical and stable isotope studies of hydrothermal alteration in the main sulfide zone of the Great Dyke,Zimbabwe and the precious metals zone of the Sonju Lake Intrusion,Minnesota, USA

Stratigraphic offsets in the peak concentrations of platinum-group elements (PGE) and base-metal sulfides in the main sulfide zone of the Great Dyke and the precious metals zone of the Sonju Lake Intrusion have, in part, been attributed to the interaction between magmatic PGE-bearing base-metal sulfide assemblages and hydrothermal fluids. In this paper, we provide mineralogical and textural evidence that indicates alteration of base-metal sulfides and mobilization of metals and S during hydrothermal alteration in both mineralized intrusions. Stable isotopic data suggest that the fluids involved in the alteration were of magmatic origin in the Great Dyke but that a meteoric water component was involved in the alteration of the Sonju Lake Intrusion. The strong spatial association of platinum-group minerals, principally Pt and Pd sulfides, arsenides, and tellurides, with base-metal sulfide assemblages in the main sulfide zone of the Great Dyke is consistent with residual enrichment of Pt and Pd during hydrothermal alteration. However, such an interpretation is more tenuous for the precious metals zone of the Sonju Lake Intrusion where important Pt and Pd arsenides and antimonides occur as inclusions within individual plagioclase crystals and within alteration assemblages that are free of base-metal sulfides. Our observations suggest that Pt and Pd tellurides, antimonides, and arsenides may form during both magmatic crystallization and subsolidus hydrothermal alteration. Experimental studies of magmatic crystallization and hydrothermal transport/deposition in systems involving arsenides, tellurides, antimonides, and base metal sulfides are needed to better understand the relative importance of magmatic and hydrothermal processes in controlling the distribution of PGE in mineralized layered intrusions of this type.     

The roles of magmatic and hydrothermal processes in PGE mineralization,Ferguson Lake deposit,Nunavut, Canada

The Ferguson Lake Ni–Cu–Co–platinum-group element (PGE) deposit in Nunavut, Canada, occurs near the structural hanging wall of a metamorphosed gabbroic sill that is concordant with the enclosing country rock gneisses and amphibolites. Massive to semi-massive sulfide occurs toward the structural hanging wall of the metagabbro, and a low-sulfide, high-PGE style of mineralization (sulfide veins and disseminations) locally occurs ~30–50 m below the main massive sulfide. Water–rock interaction in the Ferguson Lake Ni–Cu–Co–PGE deposit is manifested mostly as widespread, post-metamorphic, epidote–chlorite–calcite veins, and replacement assemblages that contain variable amounts of sulfides and platinum-group minerals (PGM). PGM occur as inclusions in magmatic pyrrhotite and chalcopyrite in both the massive sulfide and high-PGE zones, at the contact between sulfides and hornblende or magnetite inclusions in the massive sulfide, in undeformed sulfide veins and adjacent chlorite and/or epidote halos, in hornblende adjacent to hydrothermal veins, and in plagioclase–chlorite aggregates replacing garnet cemented by sulfide. The PGM are mostly represented by the kotulskite (PdTe)–sobolevskite (PdBi) solid solution but also include michenerite (PdBiTe), froodite (PdBi₂), merenskyite (PdTe₂), mertieite II (Pd₈[Sb,As]₃), and sperrylite (PtAs₂) and occur in variety of textural settings. Those that occur in massive and interstitial sulfides, interpreted to be of magmatic origin and formed through exsolution from base metal sulfides at temperatures <600°C, are dominantly Bi rich (i.e., Te-bearing sobolevskite), whereas those that occur in late-stage hydrothermal sulfide/silicate veins and their epidote–chlorite alteration halos tend to be more Te rich (i.e., Bi-bearing kotulskite). The chemistry and textural setting of the various PGM supports a genetic model that links the magmatic and hydrothermal end-members of the sulfide–PGM mineralization. The association of PGM with magmatic sulfides in the massive sulfide and high-PGE zones has been interpreted to indicate that PGE mineralization was initially formed through exsolution from base metal sulfides which formed by magmatic sulfide liquid segregation and crystallization. However, the occurrence of PGM in undeformed sulfide-bearing veins and in their chlorite–epidote halos and differences in PGM chemistry indicate that hydrothermal fluids were responsible for post-metamorphic redistribution and dispersion of PGE.     

Platinum-group element distribution in the oxidized Main Sulfide Zone, Great Dyke, Zimbabwe

In the Great Dyke mafic/ultramafic layered intrusion of Zimbabwe, economic concentrations of platinum-group elements (PGE) are restricted to sulfide disseminations in pyroxenites of the Main Sulfide Zone (MSZ). Oxidized ores near the surface constitute a resource of ca. 400 Mt. Mining of this ore type has so far been hampered due to insufficient recovery rates. During the oxidation/weathering of the pristine ores, most notably, S and Pd are depleted, whereas Cu and Au are enriched. The concentrations of most other elements (including the other PGE) remain quite constant. In the oxidized MSZ, PGE occur in different modes: (1) as relict primary PGM (mainly sperrylite, cooperite, and braggite), (2) in solid solution in relict sulfides (dominantly Pd in pentlandite, up to 6,500 ppm Pd and 450 ppm Pt), (3) as secondary PGM neoformations (i.e., Pt–Fe alloy and zvyagintsevite), (4) as PGE oxides/hydroxides that replace primary PGM as the result of oxidation, (5) hosted in weathering products, i.e., iron oxides/hydroxides (up to 3,600 ppm Pt and 3,100 ppm Pd), manganese oxides/hydroxides (up to 1.6 wt.% Pt and 1,150 ppm Pd), and in secondary phyllosilicates (up to a few hundred ppm Pt and Pd). In the oxidized MSZ, most of the Pt and Pd are hosted by relict primary and secondary PGM; subordinate amounts are found in iron and manganese oxides/hydroxides. The amount of PGE hosted in solid solution in sulfides is negligible. Considerable local variations in the distribution of PGE in the oxidized ores complicate a mineralogical balance. Experiments to evaluate the PGE recovery from oxidized MSZ ore show that using physical concentration techniques (i.e., electric pulse disaggregation, hydroseparation, and magnetic separation), the PGE are preferentially concentrated into smaller grain size fractions by a factor of 2. Highest PGE concentrations occur in the volumetrically insignificant magnetic fraction. This indicates that a physical preconcentration of PGE is not feasible and that chemical, bulk-leaching methods need to be developed in order to successfully recover PGE from oxidized MSZ ore.     

First report of platinum-group minerals from a hornblende gabbro dyke in the vicinity of the Southeast Extension Zone of the Voisey’s Bay Ni-Cu-Co deposit, Labrador

Summary This study reports the first documented occurrence of platinum group-minerals (PGM) in the vicinity of the Voisey’s Bay magmatic sulfide ore deposit. The PGM are present in a sulfide poor, hornblende gabbro dyke in the Southeast Extension Zone of the massive sulfide Ovoid deposit. The dyke has somewhat elevated concentrations of platinum-group elements (PGE) and gold (up to 1.95 g/t Pt, 1.41 g/t Pd, and 6.59 g/t Au), as well as Cu, Pb, Ag, Sn, Te, Bi and Sb. The PGM formed by magmatic processes and were little disturbed by subsequent infiltration of an externally-supplied hydrothermal fluid. To date, no similar PGM occurrences have been discovered in the Ovoid deposit itself. Whole rock REE patterns indicate that the dyke is geochemically related to the main conduit troctolites, which carry the bulk of the massive sulfide mineralization at Voisey’s Bay. The PGE mineralization is Pt- and Pd-rich, where the Pt and Pd occur predominantly as discrete PGM with minor Pd in solid solution in galena (average=1.8 ppm) and pentlandite (average=2 ppm). The discrete PGM are predominantly hosted by disseminated base-metal sulfides (bornite, chalcopyrite, and galena) (56 vol%) and are associated with other precious metal minerals (13 vol%) with only ∼3 vol% of the PGM hosted by silicate minerals. In whole rock samples, the PPGE (Pt, Pd, and Rh) correlate with abundances of chalcopyrite, bornite, galena, and other precious metal minerals (PMM), whereas the IPGE (Ir, Ru, and Rh) correlate with pyrrhotite and pentlandite. There are no correlations of the PGE with chlorine. Lead isotope compositions of galena associated with the PGE mineralization in the Southeast Extension Zone are broadly similar to those for galena in the Ovoid. The lead isotope compositions are much different from those in the Voisey’s Bay Syenite, which is a potential external hydrothermal fluid source. The observed Cu-rich, Pb-rich sulfide compositions and associated Pt-Pd-Au-Ag-Sn-Te-Bi-Sb assemblage in the dyke can be produced magmatically as late ISS differentiates (e.g., Prichard et al., 2004). Melting temperatures of the PGM are also consistent with a magmatic origin. Following crystallization of PGM from magmatic sulfide, an external REE-enriched hydrothermal fluid was introduced to the system, producing secondary amphibole and locally remobilizing the Pb and Sn from the sulfides hosting the PGM. Author’s address: M. A. E. Huminicki, Department of Earth Sciences, Memorial University of Newfoundland, St. John’s, NL, Canada A1B 3X5     

Alteration of platinum-group minerals and dispersion of platinum-group elements during progressive weathering of the Aguablanca Ni–Cu deposit, SW Spain

The distribution, mineralogy and mobility of the platinum-group elements (PGE) in the surface environment are poorly understood. This study of the lower, less altered and upper, more altered gossan, overlying the Aguablanca Ni–Cu-(PGE) magmatic deposit (Spain), has shown that the platinum-group minerals (PGM) are progressively oxidised and dispersed into iron oxides that form the gossan. A combination of the characterization of PGE in host PGM, using a scanning electron microscope, and measurement of PGE at lower concentrations in host iron oxides, using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), has for the first time allowed the total distribution of the PGE within a gossan to be documented. This study has revealed a complete in situ alteration and dispersion sequence of the PGM including (1) breakdown of both the more stable Pt-arsenides, Pt/Pd-tellurides and the less stable bismuthotellurides, (2) formation of partially oxidised PGM, (3) development of a wide range of oxidised Pt- and Pd-bearing phases, (4) subsequent formation of Fe–PGE-oxides and PGE-hydroxides, (5) incorporation of PGE into ferruginous supergene products and lastly (6) concentration of PGE at the edges of veins and iron oxides. Dispersion of Pd is greater than for the other PGE with Pd being widely distributed throughout the iron oxides. This oxidising environment produced PGE-oxides rather than PGE-alloys, also commonly found in the surface environment, especially in placers. These results provide critical evidence for the stages of mineralogical change from PGE host mineralogy in magmatic ores to surface weathering producing PGE-oxides.     

Platinum-group minerals from the Jinbaoshan Pd–Pt deposit,SW China: evidence for magmatic origin and hydrothermal alteration

The Jinbaoshan Pt–Pd deposit in Yunnan, SW China, is hosted in a wehrlite body, which is a member of the Permian (∼260 Ma) Emeishan Large Igneous Province (ELIP). The deposit is reported to contain one million tonnes of Pt–Pd ore grading 0.21% Ni and 0.16% Cu with 3.0 g/t (Pd + Pt). Platinum-group minerals (PGM) mostly are ∼10 μm in diameter, and are commonly Te-, Sn- and As-bearing, including moncheite (PtTe₂), atokite (Pd₃Sn), kotulskite (PdTe), sperrylite (PtAs₂), irarsite (IrAsS), cooperite (PtS), sudburyite (PdSb), and Pt–Fe alloy. Primary rock-forming minerals are olivine and clinopyroxene, with clinopyroxene forming anhedral poikilitic crystals surrounding olivine. Primary chromite occurs either as euhedral grains enclosed within olivine or as an interstitial phase to the olivine. However, the intrusion has undergone extensive hydrothermal alteration. Most olivine grains have been altered to serpentine, and interstitial clinopyroxene is often altered to actinolite/tremolite and locally biotite. Interstitial chromite grains are either partially or totally replaced by secondary magnetite. Base-metal sulfides (BMS), such as pentlandite and chalcopyrite, are usually interstitial to the altered olivine. PGM are located with the BMS and are therefore also interstitial to the serpentinized olivine grains, occurring within altered interstitial clinopyroxene and chromite, or along the edges of these minerals, which predominantly altered to actinolite/tremolite, serpentine and magnetite. Hydrothermal fluids were responsible for the release of the platinum-group elements (PGE) from the BMS to precipitate the PGM at low temperature during pervasive alteration. A sequence of alteration of the PGM has been recognized. Initially moncheite and atokite have been corroded and recrystallized during the formation of actinolite/tremolite, and then, cooperite and moncheite were altered to Pt–Fe alloy where they are in contact with serpentine. Sudburyite occurs in veins indicating late Pd mobility. However, textural evidence shows that the PGM are still in close proximity to the BMS. They occur in PGE-rich layers located at specific igneous horizons in the intrusion, suggesting that PGE were originally magmatic concentrations that, within a PGE-rich horizon, crystallized with BMS late in the olivine/clinopyroxene crystallization sequence and have not been significantly transported during serpentinization and alteration.     

Platinum-Group Mineral Characterization in Concentrates from High-Grade PGE Al-rich Chromitites of Korydallos Area in the Pindos Ophiolite Complex (NW Greece)

The Pindos ophiolite complex, located in the north-western part of continental Greece, hosts various podiform chromite deposits generally characterized by low platinum-group element (PGE) grades. However, a few locally enriched in PPGE + Au (up to 29.3 ppm) chromitites of refractory type are also present, mainly in the area of Korydallos (south-eastern Pindos). The present data reveal that this enrichment is strongly dependant on chromian spinel chemistry and base metal sulfide and/or base metal alloy (BMS and BMA, respectively) content in chromitites. Consequently, we used super-panning to recover PGM from the Al-rich chromitites of the Korydallos area. The concentrate of the composite chromitite sample contained 159 PGM grains, including, in decreasing order of abundance, the following major PGM phases: Pd-Cu alloys (commonly non-stoichiometric, although a few Pd-Cu alloys respond to the chemical formula PdCu₄), Pd-bearing tetra-auricupride [(Au,Pd)Cu], nielsenite (PdCu₃), sperrylite (PtAs₂), skaergaardite (PdCu), Pd-bearing auricupride [(Au,Pd)Cu₃], Pt and Pd oxides, Pt-Fe-Ni alloys, hollingworthite (RhAsS) and Pt-Cu alloys. Isomertieite (Pd₁₁Sb₂As₂), zvyagintsevite (Pd₃Pb), native Au, keithconnite (Pd₂₀Te₇), naldrettite (Pd₂Sb) and Rh-bearing bismuthotelluride (RhBiTe, probably the Rh analogue of michenerite) constitute minor phases. The bulk of PGE-mineralization is dominated by PGM grains that range in size from 5 to 10 µm. The vast majority of the recovered PPGM are associated with secondary BMS and BMA, thus confirming that a sulphur-bearing melt played a very important role in scavenging the PGE + Au content of the silicate magma from which chromian spinel had already started to crystallize. The implemented technique has led to the recovery of more, as well as noble, PGM grains than the in situ mineralogical examination of single chromitite samples. Although, the majority of the PGM occur as free particles and in situ textural information is lost, single grain textural evidence is observed. In summary, this research provides information on the particles, grain size and associations of PGM, which are critical with respect to the petrogenesis and mineral processing.     

Loypishnyun Low-Sulfide Pt–Pd Deposit of the Monchetundra Basic Massif,Kola Peninsula,Russia

The geology of the basal-structural Loypishnyun low-sulfide Pt–Pd deposit is characterized, including its mineral composition and the peculiarities of its PGE and chalcophile-element distribution in ore. The deposit is situated in the northeastern part of the Monchetundra basic massif and is localized in its lower norite–orthopyroxenite zone, intensely injected with late gabbroic rocks. Two ore zones are distinguished within the deposit. Ore zone 1 has been traced by drilling for about 1.5 km at a thickness from 10–15 to 120 m and incorporates from two to nine separate lenticular–sheetlike orebodies 0.5–25 m in thickness. Ore zone 2 has been traced for 550 m and is represented by one orebody 5–35 m thick. The internal structure of the orebodies is characterized by alternation of low-grade (Pt + Pd = 0.5–0.9 gpt), ordinary (Pt + Pd = 1.0–1.9 gpt), and high-grade (Pt + Pd > 2 gpt) interlayers of various thickness. The ores are spatially and genetically related to sulfide mineralization (pentlandite–chalcopyrite–pyrrhotite) in an amount of 1–5 vol %. The PGE distribution in ores normalized to primitive mantle is characterized by fractionation of easily fusible platinoids with a positive Pd anomaly. The spectra of chalcophile elements normalized to primitive mantle are notable for elevated Te, Bi, As, and Se contents with respect to Sn, Hg, and Pb, which reflects the significant contribution of Te, Bi, and As in the formation of platinum group minerals (PGM), whereas Se, which is devoid of proper mineral phases, most likely is an admixture in the composition of sulfides. The S/Se value in ore of the Loypishnyun deposit varies from 31 to 814. The platinum group elements (PGE) in ore are represented by 45 noble metal minerals. Ore zone 1 is characterized by lateral mineral zoning, which is expressed as replacement of a bismuthotelluride–sulfide PGM assemblage by an assemblage of copper–PGE compounds and alloys. In ore zone 2, a mineral assemblage of tellurides, copper–PGE compounds and alloys predominates, with native gold, silver, and palladium, as well as sulfides and bismuthotellurides, playing a subordinate role. The formation of PGM ore proceeded under variable sulfur fugacity conditions, beginning with the late magmatic stage at temperatures of 900–700°C and ending with hydrothermal transformation at a temperature of <500°C.     

Genesis of the Jinchuan PGE deposit, China: evidence from fluid inclusions, mineralogy and geochemistry of precious elements

Summary The Jinchuan deposit is a platinum group element (PGE)-rich sulfide deposit in China. Drilling and surface sampling show that three categories of platinum group element (PGE) mineralization occur; type I formed at magmatic temperatures, type II occurs in hydrothermally altered zones of the intrusion, and type III in sheared dunite and lherzolite. All ore types were analyzed for Os, Ir, Ru, Rh, Pd, Pt and Au, as well as for Cu, Ni, Co and S. Type I ore has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios of <7 and relatively flat chondrite-normalized noble metal patterns; the platinum group minerals (PGM) are dominated by sperrylite and moncheite associated with chalcopyrite, pyrrhotite and pentlandite. Type II has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from 40 to 330 and noble metal distribution patterns with a positive slope; the most common PGM are sperrylite and Pd bismuthotelluride phases concentrated mostly at the margins of base metal sulfides. Type III ores have the highest (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from 240 to 710; the most abundant PGM are sperrylite and phases of the Pt–Pd–Te–Bi–As–Cl system. It is concluded that the Jinchuan deposit formed as a result of primary magmatic crystallization followed by hydrothermal remobilization, transport, and deposition of the PGE.     

Stratiform platinum-group element mineralization in the layered Northern Ultramafic Center of the Lac des Iles Intrusive Complex,Ontario, Canada

The Northern Ultramafic Centre (NUC) of the Lac des Iles Complex, Northwest Ontario hosts several platinum group element (PGE) occurrences, including the Sutcliffe Zone, which consists of four subparallel, stratiform PGE-enriched intervals exposed within the cyclically layered eastern flank of the NUC. Field relationships, mineral paragenesis and lithogeochemistry allowed for the identification of 14 cyclic cumulate sequences of two distinct types – Cyclic unit type A (CUA) and Cyclic unit type B (CUB). CUA-type and CUB-type units are interpreted to have formed from a Si-enriched and Si-poor parent magmas, respectively. PGE-enriched intervals occur in four of the CUA-type cyclic units (CUA-5, -6, -8 and -11). PGE enriched intervals are commonly associated with websterite, olivine websterite and gabbronorite containing primary disseminated sulfide (0.2–2 vol%) which are dominated by pyrrhotite, chalcopyrite, and pentlandite with minor cubanite, and troilite. In hydrothermally altered rocks enriched in PGE, primary sulfides are locally partially replaced by secondary chalcopyrite, sphalerite, heazlewoodite, and chalcocite. Palladium occurs either in solid solution with primary pentlandite or is associated with platinum group minerals (PGM) such as Pd-plumbide, Pd-telluride, and Pt-bismuthotelluride. PGMs commonly occur within primary sulfides, at contacts between primary sulfide–silicate minerals, or in association with secondary serpentine and actinolite. Gold and silver typically occur as electrum that exhibits similar textural characteristics and mineralogical associations as the PGMs.Two different chemostratigraphic patterns of PGE, Cu and S enrichment can be recognized among the mineralized CUA cycles: The first (top-loaded) occurs near the top of CUA cycles (CUA-6, -8 and -11) in websterite and/or gabbronorite, just below the levels at which CUB magmas were emplaced. The second (middle-loaded), occurs midway through the lower cycle (CUA-5) in the olivine websterite, which is overlain by CUA-6. Within the four mineralized intervals, PGE tenors average 643 ppm Pd + Pt (in 100% sulfide), Pd/Pt and Pd/Ir ratios range from 0.9 to 3.5 and 35 to 537, respectively, and S/Se ratios range between 500 and 6000. The highest PGE tenors (4377 ppm Pd + Pt) are found in the lowermost interval in serpentinized olivine websterite and have an average Pd/Pt ratio of 3.5 and a S/Se ratio of approximately 2000.It is proposed that orthomagmatic processes of fractional crystallization and dynamic magma recharge were the dominant mineralization processes triggering sulfide-saturation and PGE concentration at the Sutcliffe Zone. Textural relationships between PGM, sulfide minerals, and primary and secondary hydrous silicates suggest that late magmatic to postcumulus hydrothermal fluid infiltration occurred locally during and after sulfide mineralization of the PGE-enriched intervals. However, these fluids had a minimal effect on the distribution of PGE in the Sutcliffe Zone. The Sutcliffe Zone shares many similarities with classic stratiform PGE deposits in terms of Pd/Pt ratio, high PGE tenors, low abundance of sulfide, and PGM assemblages. However, it is distinguished from most stratiform PGE deposits by its tectonic environment and lithostratigraphic position and by the intimate spatial association of the two parental magmas that are interpreted to have been responsible for the observed chemostratigraphy and PGE enrichment.     

Alteration of Platinum-Group and Base-Metal Mineral Assemblages in Ophiolite Chromitites from the Dobromirtsi Massif,Rhodope Mountains (Bulgaria)

The Dobromirtsi Ultramafic Massif, located in the Rhodope Mountains (SE Bulgaria), is a portion of a Paleozoic sub-oceanic mantle affected by polyphase regional metamorphism. This massif contains several small, podiform chromitite bodies which underwent the same metamorphic evolution as their host peridotites. Like other ophiolite chromitites, those found in Dobromirtsi carry abundant platinum-group minerals (PGM) and base-metal minerals (BMM). The PGM consist mainly of Ru-, Os-, and Ir-based PGM (laurite RuS₂-erlichmanite OsS₂, Os-Ru-Ir alloys, irarsite [IrAsS], Ru-rich pentlandite, and an unknown Ir-sulfide) but minor Rh- and Pd-based PGM (hollingworthite [RhAsS] and a series of unidentified stannides and sulfantimonides) are also present. In contrast, the BMM are dominated by pentlandite (Ni,Fe)₉S₈, followed by heazlewoodite (Ni₃S₂), breithauptite (NiSb), maucherite (Ni₁₁As₈), godlevskite (Ni₇S₆), gersdorffite (NiAsS), millerite (NiS), undetermined minerals containing Ni, As and Sb, orcelite (Ni_5-XAs₂), awaruite (Ni₃Fe) and chalcopyrite (CuFeS₂). The detailed study of the textural relationships, morphology and composition of the PGM and BMM inclusions indicate the existence of two different PGM-BMM assemblages: (i) a primary or magmatic; and (ii) a secondary related with postmagmatic alteration. The PGM and BMM inclusions in unaltered zones of chromite crystals (mainly laurite-erlichmanite and pentlandite) are considered to be primary magmatic minerals formed under variable temperature (1200–1100°C) and sulfur fugacity (between −2 and −0.5 log fS₂). In contrast, PGM and BMM located along altered edges of chromite and serpentinised silicate matrix are considered to be secondary, formed from or re-equilibrated with altering fluids. Secondary PGM and BMM assemblages are considered as result of the combination of reducing and oxidising events related with regional metamorphism. Under low fO₂ states, fS₂ also drops giving place to the formation of S-poor Ni-rich sulfides and secondary Ru-alloys by desulfurisation of primary S-containing minerals. In contrast, predominance of platinum-group elements and/or base-metal arsenides and sulfarsenides associated with the altered edges of chromite (chromite strongly enriched in Fe₂O₃) is related with the fixing of remobilised PGE (mainly Ir, Rh and Pd) and base-metals (mainly Ni and Fe) when late oxidising fluids supplied As as well as Sb and Sn.     

Sulfide petrology and highly siderophile element geochemistry of abyssal peridotites: a coupled study of samples from the Kane Fracture Zone (45°W 23°20N, MARK area, Atlantic Ocean)

Nineteen samples from the Kane Fracture Zone have been studied for sulfide mineralogy and analyzed for S, Se, platinum-group elements (PGE), and Au to assess the effect of refertilization processes on the PGE systematics of abyssal peridotites. The lherzolites show broadly chondritic PGE ratios and sulfide modal abundances (0.01 to 0.03 wt%) consistent with partial melting models, although the few pyroxene-hosted sulfide inclusions and in situ LAM-ICPMS analyses provide evidence for in situ mobilization of a Cu-Ni-rich sulfide partial melt. The most refractory harzburgites (spinel Cr# > 29) are almost devoid of magmatic sulfides and show uniformly low Pd_N/Ir_N (<0.5) for variable Pt_N/Ir_N (0.8 to 1.2). The compatible behavior of Os, Ir, Ru, Rh, and Pt reflects the presence of primary Os-Ru alloys. Some harzburgites displaying petrographic evidence for refertilization by incremental melts en route to the surface are enriched in sulfides (up to 0.1 wt%). Some of these sulfides are concentrated in small veinlets of clinopyroxene and spinel crystallized from these melts. These S-rich harzburgites display superchondritic Pd_N/Ir_N (up to 2.04) positively correlated with sulfide modal contents. It is concluded that refertilization processes resulting in precipitation of metasomatic sulfides may significantly enhance Pd concentrations of abyssal peridotites while marginally affecting Pt (Pt_N/Ir_N ≤ 1.24) and Rh (Rh_N/Ir_N ≤ 1.23) as well. When the effects of such processes are screened out, our database suggests PGE relative abundances in the DMM (Depleted MORB Mantle; MORB: Mid-Ocean Ridge) within the uncertainty range of chondritic meteorites, without evidence of superchondritic Pt/Ir and/or Rh/Ir ratios.     

Chemical composition of platinum-group minerals from the Bor-Uryakh massif (Maimecha-Kotui Province,Russia)

This contribution firstly presents particularities of mineral chemistry of platinum-group elements (PGE) mineralization from placer deposits linked to the Bor-Uryakh massif of the Maimecha-Kotui Province, northern part of the Siberian Craton. The chemical composition of PGE mineralization has been studied by electron microprobe analysis. At Bor-Uryakh, main platinum-group minerals (PGM) comprise Os-Ir and Pt-Fe alloys represented by individual crystals, and polyphase PGM assemblages. The majority (e.g., 12 out of 19) of the Os-rich nuggets are iridian osmium, with subordinate amounts of native osmium (Os) and chengdeite (Ir₃Fe). Pt-Fe alloys have a stoichiometric composition close to Pt₂Fe. According to the nomen-clature by L. Cabri and C. Feather [1975] these minerals correspond to ferroan platinum. Based on geological position and geochemical features of investigated PGE mineralization the particular rock sources have been established. This study has demonstrated the similarity of chemical characteristics of Os-Ir and Pt-Fe alloys of the Bor-Uryakh massif to those of PGM from the Guli massif (Maimecha-Kotui Province), platiniferous zoned-type ultramafic massifs (e.g., Kondyor, Inagli and Chad) of the Aldan Province and Platinum belt of the Urals (Nizhny Tagil, Kytlym, etc.).     

PGE mineralization of dunite-wehrlite massifs at the Gutara-Uda interfluve, Eastern Sayan

The Pt-Pd and Au-Ag mineralization hosted in both wehrlite without visible links to sulfide mineralization (dispersed assemblage of the Tartai massif) and disseminated Cu-Ni sulfide ore (ore assemblage of the Ognit massif) was found in dunite-wehrlite massifs localized in the fold framework of the Siberian Craton. The Pt minerals in both assemblages comprise sperrylite (PtAs₂) and secondary Pt-Fe-Ni alloys in the Ognit massif and Pt-Fe-Cu and Pt-Cu alloys in the Tartai massif. The Pd minerals are widespread in the ore assemblages as compounds with Te, Sb, and Bi, whereas in the dispersed assemblage Pd is concentrated primarily in Pd-Cu-Sb compounds. Both assemblages are characterized by similar substitution of sperrylite with orcelite (Ni_{5 ? x}As₂) and then with secondary Pt-Fe-Ni or Pt-Fe-Cu and Pt-Cu alloys; the occurrence of Au-Ag alloys with prevalence of Ag over Au; and replacement of them with auricupride (Cu₃Au) at the late stage. Sperrylite in both assemblages contains Ir impurities, while the Pd minerals contain Cu and Ni admixtures, which are typical of mineral assemblages related to the ultramafic intrusions with nickel specialization. PGM were formed under a low sulfur fugacity and high As, Bi, and Sb activities. The postmagmatic fluids affected the primary mineral assemblages under reductive conditions, and this effect resulted in replacement of sperrylite with Ni arsenide (orcelite) and Pt-Fe-Ni and Pt-Fe-Cu alloys; Ni and Cu sulfides were replaced with awaruite and native copper.     

Platinum-group mineral assemblage of the Prizhimny Creek (Koryak Highland)

In the alluvial deposits of the Prizhlimny Creek (southern part of the Koryak Highland), grains of platinum-group minerals are found along with gold. We have established that the grains are native platinum (Pt, Fe) containing Cu (up to 5 wt.%), Os (up to 8 wt.%), and Rh (up to 2 wt.%). Inclusions in the platinum are native osmium (the content of Ir impurity reaches 12 wt.%, the average content being 0.2–4 wt.%), an unnamed intermetallic compound of composition PtRh, sulfides and arsenides of PGE (cooperite, laurite, malanite, cuproiridsite, cuprorhodsite, sperrylite, hollingworthite, unnamed compounds PdS, (Ir,Ru)S₂, (Ir,Pt)S₂, Cu, and Fe (bornite, chalcopyrite), chromite, and Cr-magnetite. Replacement of native-osmium crystals by compound IrO₂ is described. It has been established that this compound formed during oxidation accompanied by the replacement of isoferroplatinum by native platinum. The data obtained agree with the results of study of platinum-group mineral assemblages from placers localized in weakly eroded Ural–Alaskan-type massifs whose apical parts formed under high oxygen activity conditions. Clinopyroxenites of the Prizhimny massif are considered to be the potential source of PGE.