Inclusions in an isoferroplatinum nugget from the Freetown Layered Complex, Sierra Leone

2018 ◽  
Vol 82 (3) ◽  
pp. 577-592 ◽  
Author(s):  
John F. W. Bowles ◽  
Saioa Suárez ◽  
Hazel M. Prichard ◽  
Peter C. Fisher

ABSTRACTInclusions of platinum-group minerals (PGM) within alluvial isoferroplatinum nuggets from the Freetown Peninsula, Sierra Leone, are aligned with their shape determined by the structure of their host. The edges of the majority of the inclusions lie at 0°, 45° or 90° to external crystal edges of the nugget which shows that the inclusions are not randomly oriented earlier minerals incorporated within their host. The inclusions are later infills, probably formed at the surface of the nugget during growth and subsequently enclosed by the growing nugget. PGM on the present surface of the nugget represent the last stage of this partnership. A single nugget containing abundant inclusions is described here but similar features are observed in other nuggets from the same area. The inclusions contain laurite (RuS2), irarsite–hollingworthite (IrAsS–RhAsS), Pd–Te–Bi–Sb phases, Ir-alloy, Os-alloy, Pd-bearing Au, an Rh–Te phase, Pd–Au alloy and Pd–Pt–Cu alloy. PGM found on the nugget surface include laurite, irarsite and cuprorhodsite (CuRh2S4). The Pd–Te–Bi–Sb phases may include Sb-rich keithconnite (Pd20S7) and compositions close to the kotulskite–sobolevskite solid-solution series (PdTe–BiTe). Textural evidence suggests that formation of the nuggets began with the isoferroplatinum host and the voids were filled starting intergrowths of laurite and irarsite–hollingworthite with both laurite and irarsite–hollingworthite often showing compositional zonation and each of them replacing the other. Filling of the voids probably continued with Pd-Cu-bearing gold, Sb-rich keithconnite (Pd,Pt)20.06(Te,Sb,Bi)6.94, keithconnite, telluropalladinite Pd9(Te,Bi)4, RhTe and finally Ir-alloy and then Os-alloy. The nuggets are thought to be neoform growths in the organic- and bacterial-rich soils of the tropical rain forest cover of the Freetown intrusion. The mineralogical assemblage in the layered gabbros of the intrusion has been previously shown to differ from the alluvial assemblage in the rivers and these inclusions, not seen in Pt3Fe in the unaltered rocks, add a further item to the catalogue of differences.

2017 ◽  
Author(s):  
Sara Callegaro ◽  
◽  
Andrea Marzoli ◽  
Hervé Bertrand ◽  
Janne Blichert-Toft ◽  
...  

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.


1997 ◽  
Vol 61 (406) ◽  
pp. 367-375 ◽  
Author(s):  
I. C. Lyon ◽  
H. Tamana ◽  
D. J. Vaughan ◽  
A. J. Criddle ◽  
J. M. Saxton ◽  
...  

AbstractPlatinum-group minerals (PGM) from placer deposits in Colombia, California, Oregon and Alaska were investigated with the electron microprobe, proton microprobe (μ-PIXE) and ion probe to analyse their major and trace element contents and 187Os/186Os isotopic ratios. Most of the grains in the samples investigated proved to be essentially homogeneous alloys of Pt-Fe and Os-Ir-Ru although a few of them contained inclusions of other PGM such as cooperite and laurite. Detailed analyses were undertaken on the Os-Ir-Ru alloy phases.The 187Os/186Os isotope ratios fell into a range from 1.005 to 1.156 and are consistent with data published on PGM from other placer deposits from these regions. The ratios, together with the trace element data (and in particular the low rhenium content) determined by ion probe and μ-PIXE, indicate that crustal osmium was not incorporated in the grains and that no significant evolution of the 187Os/186Os ratios occurred during their history. These data, along with mineralogical and textural evidence, are consistent with a mantle origin for the grains through ultramafic intrusions, although the data do not entirely rule out alternative interpretations.


1990 ◽  
Vol 54 (376) ◽  
pp. 413-418 ◽  
Author(s):  
H. A. Buckley ◽  
A. R. Woolley

AbstractCarbonates of the magnesite-siderite series have been found and analysed in carbonatites from the Lueshe, Newania, Kangankunde, and Chipman Lake complexes. This series has been represented until now only by a few X-ray identifications of magnesite and three published analyses of siderite and breunnerite (magnesian siderite). Most of the siderite identified in carbonatites in the past has proved to be ankerite, but the new data define the complete solid-solution series from magnesite to siderite. They occur together with dolomite and ankerite and in one rock with calcite. The magnesites, ferroan magnesites and some magnesian siderites may be metasomatic/hydrothermal in origin but magnesian siderite from Chipman Lake appears to have crystallized in the two-phase calcite + siderite field in the subsolidus CaCO3-MgCO3-FeCO3 system. Textural evidence in Newania carbonatites indicates that ferroan magnesite, which co-exists with ankerite, is a primary liquidus phase and it is proposed that the Newania carbonatite evolved directly from a Ca-poor, Mg-rich carbonatitic liquid generated by partial melting of phlogopite-carbonate peridotite in the mantle at pressures >32 kbar.


1999 ◽  
Vol 63 (3) ◽  
pp. 345-352 ◽  
Author(s):  
I. McDonald ◽  
D. Ohnenstetter ◽  
M. Ohnenstetter ◽  
D. J. Vaughan

AbstractSmall (<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.


2017 ◽  
Vol 58 (9) ◽  
pp. 1811-1840 ◽  
Author(s):  
Sara Callegaro ◽  
Andrea Marzoli ◽  
Hervé Bertrand ◽  
Janne Blichert-Toft ◽  
Laurie Reisberg ◽  
...  

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