Platinum-group minerals from Seyba, Eastern Sayans, Russia, and substitutions in the PGE-rich pentlandite and ferhodsite series

2019 ◽  
Vol 83 (4) ◽  
pp. 531-538
Author(s):  
Andrei Y. Barkov ◽  
Gennadiy I. Shvedov ◽  
Andrey A. Nikiforov ◽  
Robert F. Martin

AbstractChromitite 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.

Minerals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 545
Author(s):  
Andrei Y. Barkov ◽  
Nadezhda D. Tolstykh ◽  
Robert F. Martin ◽  
Andrew M. McDonald

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.


2021 ◽  
Author(s):  
Olga Kiseleva ◽  
Yuriy Ochirov ◽  
Sergey Zhmodik ◽  
Brian Nharara

<p>The studied area is in the southeastern region of Eastern Sayan. Several tectonically dissected ophiolite complexes were exposed along the margin of the Gargan block and tectonically thrust over this block. Placer nuggets of PGE alloys from the Kitoy river were examined using a scanning electron microscope. Platinum-group minerals (PGM's) in placer deposits provide vital information about the types of their primary source rocks and ores as well as the conditions of formation and alteration. The primary PGM's are Os-Ir-Ru alloys, (Os, Ru)S<sub>2</sub>, and (Os, Ir, Ru)AsS. (Os, Ru)S<sub>2</sub> form overgrowth around the Os-Ir-Ru alloys. The secondary, remobilized PGM's are native osmium, (Ir-Ru) alloys, garutite (Ir, Ni, Fe), zaccarinite (RhNiAs), selenides, tellurides (Os, Ir, Ru), and non-stoichiometric (Pd, Pt, Fe, Te, Bi) phases (Fig.1). Secondary PGM's (garutite and RhNiAs) form rims around Os-Ir-Ru alloys, intergrowth with them, or form polyphase aggregates. Such PGM's (identical in composition and microstructure) are also found in chromitites from Neoproterozoic ophiolite massifs of Eastern Sayan (Kiseleva et al., 2014; 2020). Platinum-metal minerals, exotic for ophiolites, are found among secondary PGM's such as selenides and tellurides (Os, Ir, Ru), (Pt, Pd)<sub>3</sub>Fe, Pd<sub>3</sub>(Te, Bi), (Au, Ag), and non-stoichiometric (Pd, Pt, Fe, Te, Bi) phases. They occur as inclusions in the Os-Ir-Ru alloys or fill cracks in crushed grains of primary PGM's. PGM's in placer deposits of the Kitoy river are similar to the mineral composition of PGE in chromitites of the Ospa-Kitoy ophiolitic massif, which contain Pt-Pd minerals and Pt impurities in Os-Ir-Ru alloys (Kiseleva et al., 2014). Selenides (Os-Ir-Ru) are rare within PGM's from ophiolite chromitites (Barkov et al., 2017; Airiyants et al., 2020) and also occur in chromitites of the Dunzhugur ophiolite massif (Kiseleva et al., 2016). Features of selenides and tellurides (Os, Ir, Ru) indicate their late formation as a result of the influence of magmatic and metamorphic fluids on primary PGE alloys. The filling of cracks in crushed (Os-Ir-Ru) alloys indicates that selenides and tellurides formed during tectonic deformation processes. The source of platinum-group minerals from the Kitoy river placer is the Ospa-Kitoy ophiolite massif, and primarily chromitites.</p><p><img src="https://contentmanager.copernicus.org/fileStorageProxy.php?f=gepj.eb9553e3c70065361211161/sdaolpUECMynit/12UGE&app=m&a=0&c=f3ccc1c7cf7d06094d2afaa34fe9d9a1&ct=x&pn=gepj.elif&d=1" alt=""></p><p>Figure 1. BSE microphotographs of PGM from from alluvial placers of the Kitoy river</p><p>Mineral chemistry was determined at the Analytical Centre for multi-elemental and isotope research SB RAS. This work supported by RFBR grants: No. 16-05-00737a,  19-05-00764а, 19-05-00464a and the Russian Ministry of Education and Science</p><p>References</p><p>Airiyants E.V., Belyanin D.K., Zhmodik S.M., Agafonov L.V., Romashkin P.A.  // Ore Geology Reviews. 2020. V. 120. P.  103453</p><p>Barkov A.Y., Nikiforov A.A., Tolstykh N.D., Shvedov G.I., Korolyuk V.N. // European J. Mineralogy. 2017. V.29(9). P.613-621.</p><p>Kiseleva O.N., Zhmodik S.M., Damdinov B.B., Agafonov L.V., Belyanin D.K. // Russian Geology and Geophysics. <strong>2014</strong>. V. 55. P. 259-272.</p><p>Kiseleva O.N., Airiyants E.V., Belyanin D.K., Zhmodik S.M., Ashchepkov I.V., Kovalev S.A. // Minerals. 2020. V. 10. N 141. P. 1-30.</p><p>Kiseleva O.N., Airiyants E.V., Zhmodik S.M., Belyanin D.K / Russian and international conference proceedings “The problems of geology and exploitation of platinum metal deposits” – St.Petersburg: Publishing house of St.Petersburg State University. 2016. 184 P.</p>


1992 ◽  
Vol 29 (2) ◽  
pp. 209-221 ◽  
Author(s):  
Roland K. W. Merkle

The platinum-group minerals in a drill core taken through the middle group of chromitite layers in the Critical Zone at Marikana in the western Bushveld Complex were found to consist mainly of laurite as inclusions in chromite grains. The platinum-group minerals containing Pt, Pd, and Rh are concentrated in the intercumulus silicates and frequently associated with base-metal sulphides. Up to about 20% of all platinum-group minerals in the investigated chromitite layers contain sub stantial amounts of As. The base-metal sulphides are strongly modified in the postmagmatic stage, which led to a significant loss of Fe and S, in this way concentrating Cu, Ni, and the platinum-group elements by factors of up to 10. Interaction between chromite and base-metal sulphides cannot account for all the Fe lost in chromite-poor samples, and the importance of additional processes is indicated. Inclusions in chromite and orthopyroxene indicate the formation of discrete platinum-group minerals and As-rich phases before the formation of an immiscible sulphide melt. Resorption of earlier formed platinum-group minerals into the immiscible sulphide melt and postmagmatic sulphidation destroyed most of the evidence of the early formed platinum-group minerals.


Minerals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 21
Author(s):  
Evgenia V. Airiyants ◽  
Olga N. Kiseleva ◽  
Sergey M. Zhmodik ◽  
Dmitriy K. Belyanin ◽  
Yuriy C. Ochirov

The platinum-group minerals (PGM) in placer deposits provide important information on the types of their primary source rocks and ores and formation and alteration conditions. The article shows for the first time the results of a study of placer platinum mineralization found in the upper reaches of the Kitoy River (the southeastern part of the Eastern Sayan (SEPES)). Using modern methods of analysis (scanning electron microscopy), the authors studied the microtextural features of platinum-group minerals (PGM), their composition, texture, morphology and composition of microinclusions, rims, and other types of changes. The PGM are Os‑Ir‑Ru alloys with a pronounced ruthenium trend. Many of the Os‑Ir‑Ru grains have porous, fractured, or altered rims that contain secondary PGE sulfides, arsenides, sulfarsenides, Ir-Ni-Fe alloys, and rarer selenides, arsenoselenides, and tellurides of the PGE. The data obtained made it possible to identify the root sources of PGM in the placer and to make assumptions about the stages of transformation of primary igneous Os-Ir-Ru alloys from bedrock to placer. We assume that there are several stages of alteration of high-temperature Os-Ir-Ru alloys. The late magmatic stage is associated with the effect of fluid-saturated residual melt enriched with S, As. The post-magmatic hydrothermal stage (under conditions of changing reducing conditions to oxidative ones) is associated with the formation of telluro-selenides and oxide phases of PGE. The preservation of poorly rounded and unrounded PGM grains in the placer suggests a short transport from their primary source. The source of the platinum-group minerals from the Kitoy River placer is the rocks of the Southern ophiolite branch of SEPES and, in particular, the southern plate of the Ospa-Kitoy ophiolite complex, and primarily chromitites.


2021 ◽  
Vol 59 (6) ◽  
pp. 1511-1542
Author(s):  
Yiguan Lu ◽  
C. Michael Lesher ◽  
Liqiang Yang ◽  
Matthew I. Leybourne ◽  
Wenyan He ◽  
...  

ABSTRACT The Jinbaoshan platinum group element-(Cu)-(Ni) deposit in southwest China is a sulfide-poor magmatic platinum-group element deposit that experienced multiple phases of post-magmatic modification. The sulfide assemblages of most magmatic Ni-Cu-platinum-group element deposits in China and elsewhere in the world are dominated by pentlandite-pyrrhotite-chalcopyrite with lesser magnetite and minor platinum-group minerals. However, Jinbaoshan is characterized by (1) hypogene violarite-pyrite 1-millerite-chalcopyrite and (2) supergene violarite-(polydymite)-pyrite 2-chalcopyrite assemblages. The platinum-group minerals are small (0.5–10 μm diameter) and include moncheite Pt(Te,Bi)2, mertieite-I Pd11(Sb,As)4, the atokite Pd3Sn – rustenburgite Pt3Sn solid solution, irarsite IrAsS, and sperrylite PtAs2 hosted mainly by violarite, silicates (primarily serpentine), and millerite. The platinum-group minerals occur in two sulfide assemblages: (1) mertieite-I-dominant (with irarsite, palladium, and Pd-alloy) in the hypogene assemblage and (2) moncheite-dominant (with irarsite, sperrylite, and atokite) in the supergene assemblage. Palladium and intermediate platinum-group elements (Os, Ir, Ru) are concentrated mainly in violarite, polydymite, and pyrite 2. Platinum is seldom hosted by base metal sulfides and occurs mainly as discrete platinum-group minerals, such as moncheite, sperrylite, and merenskyite. Violarite and polydymite in the Jinbaoshan deposit contain more Pb-Ag than pentlandite and pyrrhotite in the Great Dyke and Lac des Iles deposit. The formation of the sulfide assemblages in Jinbaoshan can be interpreted to have occurred in three stages: (1) a magmatic Fe-Ni-Cu sulfide melt crystallized Fe-Ni monosulfide and Cu-rich intermediate solid solutions, which inverted to a primary pyrrhotite-pentlandite-chalcopyrite-magnetite assemblage; (2) an early-secondary hypogene voilarite-millterite-pyrite 1-chalcopyrite assemblage formed by interaction with a lower-temperature magmatic-hydrothermal deuteric fluid; and (3) a late-secondary supergene violarite-polydymite-pyrite 2-chalcopyrite assemblage formed during weathering. Late-magmatic-hydrothermal fluids enriched the mineralization in Pb-Ag-Cd-Zn, which are incompatible in monosulfide solid solution, added Co-Pt into violarite, and expelled Pd to the margins of hypogene violarite and millerite, which caused Pd depletion in the hypogene violarite and the formation of mertieite-I. Supergene violarite inherited Pd and intermediate platinum-group elements from primary pentlandite. Thus, the unusual sulfide assemblages in the Jinbaoshan platinum-group element-(Cu)-(Ni) deposit results from multiple overprinted post-magmatic processes, but they did not significantly change the chalcophile element contents of the mineralization, which is interpreted to have formed at high magma:sulfide ratios (R factors) through interaction of crustally derived sulfide and a hybrid picritic-ferropicritic magma derived from subduction-metasomatized pyroxenitic mantle during impingement of the Emeishan plume on the Paleo-Tethyan oceanic subduction system.


Minerals ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 365 ◽  
Author(s):  
Andrei Y. Barkov ◽  
Federica Zaccarini

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) [...]


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