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Explor. Mining Geol., Vol. 5, No. 2, pp. 73-167, 1996 Copyright © 1996 Canadian Institute of Mining, Metallurgy and Petroleum Pergamon Printed in Great Britain. All rights reserved PII: S0964-1823(96)00012-8 0964-1823/96 $15.00 + o.oo Mineralogy and Distribution of Platinum-group Mineral (PGM) Placer Deposits of the World LOUIS J. CABRI Canada Centre for Mineral and Energy Technology 555 Booth Street, Ottawa, Ontario, Canada, K1A 0G1 DONALD C. HARRIS* Geological Survey of Canada 601 Booth Street, Ottawa, Ontario, Canada, K1A0E8 THOROLF W. WEISER Federal Institute for Geosciences and Natural Resources Stilleweg 2, 30655 Hannover, Germany Received January 18, 1996; accepted March 26, 1996. ^Present address: 23 Bentworth Crescent, Nepean, Ontario, Canada, K2G fXl Panning for platinum, Tapitangan River, Banggi Island, North Borneo, Malaysia Explor. Mining Geol., Vol. 5, No. 2, 1996 Abstract—Mineralogical studies of platinum-group minerals (PGM) made during the period 1970- 1995 are compiled in this paper for PGM obtained from platinum- and gold-bearing placer deposits of fifteen countries. A total of 3399 quantitative electron microprobe analyses of 37 different PGM are presented, together with analytical data plotted on compositional diagrams. The data reflect the dominance of Pt-Fe alloys (1723 analyses) and Os-Ir-Ru-Pt alloys (976 analyses) in the placers. The platinum-group element (PGE) alloys, as well as some other PGM, generally occur as grains less than one millimetre in size. The Pt-Fe alloys, containing some Cu and Ni, are characterized by a wide range of Pt:(Fe, Cu, Ni) ratios and, where sufficient data are available, often show a bimodal popu­ lation at about 16-17 and 25 at.% (Fe, Cu, Ni). Iridium, osmium, and rhodium occur in trace quan­ tities in over 96% of the analyzed grains, and all three elements were never found to be in concen­ trations below their detection levels simultaneously. The large data base for the hexagonal alloys shows a well-developed trend parallelling the irascibility gap in the Os-Ir-Ru ternary system. New analyses have narrowed further the width of this miscibility gap, which we postulate to be due to the formation of some alloys at higher temperatures. Important features of the PGM alloys studied include the presence of inclusions of other PGM (as well as some undefined PGM), PGE-bearing minerals, spinels, silicates, and more rarely sulfides such as chalcopyrite, bornite, and pentlandite, as well as their crystallographic orientation and tex­ tures. Alteration and replacement features (when present) are minor, not pervasive, and usually restricted to a limited number of PGM. The sum of the features obtained by detailed mineralogical characterization of the placer PGM is consistent with a high temperature intrusive origin. Evidence of minor secondary alteration that is sometimes found (e.g., irarsite, tulameenite) is probably asso­ ciated with later processes such as serpentinization. The presence of PGE-oxides and hydroxides (?), all of which are still incompletely characterized, is ascribed to surficial weathering processes. In many cases the placer PGM can be traced to the source intrusive rocks (e.g., zoned ultramafic com­ plex, ophiolite). However, correlation with source rocks is sometimes not possible due to deep weathering, lack of detailed geological maps, or inacessible field areas. Copyright © 1996 Canadian Institute of Mining, Metallurgy and Petroleum. CONTENTS ABSTRACT......................................................................................................................................74 INTRODUCTION............................................................................................................................76 ANALYTICAL TECHNIQUES............................................................. .......................................76 NOMENCLATURE OF PLATINUM-GROUP ELEMENT (PGE) Al .I .OYS...............................78 NOMENCLATURE OF PLATINUM-IRON ALLOYS...................................................................78 MINERALOGY OF PLATINUM-GROUP MINERALS (PGM) IN PLACER DEPOSITS.........78 ORIGIN OF PGM IN ELUVI ALAND ALLUVIAL PLACER DEPOSITS.................................81 DESCRIPTIONS OF INDIVIDUAL PGM PLACER DEPOSITS................................................82 Canada Yukon, Florence Creek.................................................................................................................82 Northwest Territories, Liard River...............................................................................................83 British Columbia Atlin Area..................................................................................................................................84 Quesnel River Area...................................................................................................................84 Tulameen River Area................................................................................................................84 Alberta, Edmonton, North Saskatchewan River..........................................................................89 Saskatchewan, near North Battleford, North Saskatchewan River.............................................90 Burma Chindwin River Area....................................................................................................................90 Nawngkettha.............................................................................................................................90 Nawngpusawng.........................................................................................................................91 Myenga.......................................Г............................................................................................91 Mineralogy and Distribution of PGM Placer Deposits of the World • L.J. Cabri et al. 75 Manawtha.................................................................................................................................94 Tanga........................................................................................................................................95 Kyain........................................................................................................................................95 Indawgyi Lake.........................................................................................................................95 Wunbe In..................................................................................................................................95 Malaysia Borneo, Sabah Province..............................................................................................................95 Indonesia Borneo, South Kalimantan, Riam Kanan....................................................................................96 Papua New Guinea.....................................................................................................................97 Russia Urals..............................................................................................................................................98 Sissert, Omutnaya River...........................................................................................................98 Sissert........................................................................................................................................98 Kushvinskij...............................................................................................................................99 Nizhni Tagil..............................................................................................................................99 Nevyansk.................................................................................................................................100 Western Chukot...........................................................................................................................100 Thrkey ' - Kars Province, Eastern Anatolia, Ortakale River.......................................................................101 United States Alaska, Fox Gulch......................................................................................................................101 California....................................................................................................................................102 Australia Tasmania.....................................................................................................................................102 Brazil Minas Gerais, Itabira..................................................................................................................103 Colombia Choco Region, Rio Condoto Area..............................................................................................103 El Paso....................................................................................................................................104 Viravira....................................................................................................-.............................104 Delfin.......................................................................................................................................Ю5 Nevado....................................................................................................................................105 Ecuador Esmeraldas Province, Santiago River.........................................................................................110 Ethiopia Birbir River, Joubdo Stream.......................................................................................................Ill Sierra Leone Freetown Complex......................................................................................................................114 South Africa Transvaal and Orange Free State................................................................................................117 COMMON ACCESSORY PGM....................................................................................................118 UNDEFINED PGM AND PGM OXIDES.....................................................................................118 CONCLUSIONS.............................................................................................................................118 ACKNOWLEDGMENTS..............................................................................................................120 BIBLIOGRAPHY...........................................................................................................................122 APPENDIX A — REFERENCES FOR LOCATION MAP OF PGM PLACER DEPOSITS......129 APPENDIX В — TABLES OF ELECTRON MICROPROBE ANALYSES OF PGM...............132 76 Explor. Mining Geol., Vol. 5, No. 2, 1996 Introduction community today. The purpose of the present paper is to compile all the authors’ previously published and new data \ Until the early 20th century, placer deposits containing on PGM found in placer (and eluvial) deposits in the context platinum-group minerals (PGM) were the principal source of their worldwide distribution, in the hope that this will of platinum-group elements (PGE) for nearly two hundred provide a useful database in the areas of PGE geochemistry years, and often were mined as a by- or co-product of plac­ and exploration for PGE deposits. Many placer deposits er gold. In some gold placer operations, mercury amalga­ have been examined by other workers, for which localities mation is a common practice for gold extraction and this and comprehensive reference lists are given in this report imparts a silver metallic luster to the gold that can be easily (the data are not included). However, it is acknowledged mistaken for PGM, or the PGM can be overlooked because that there may be other published data on platinum-bearing of mercury amalgamation. Placer mining is reported to have placer deposits of which we are not aware, especially for begun in Colombia in the mid-1700s, followed by Russia in China and the former U.S.S.R. The worldwide localities of 1822-24. With the discovery and exploitation of PGE in Cu- the placer deposits which we and others have examined are Ni sulfide ores in the early 20th century, production from shown in Figure 1. References to the various PGM placer alluvial deposits decreased to the extent that approximately localities, with an indication as to whether analyses or other 99% of current primary PGE production comes from sulfide data are available, are listed in Appendix A. ores. The placer deposits which once were the world’s This paper provides the reader with the largest single largest producers of placer PGE are closely related to long source of mineralogical and petrological data on PGM and tectonic belts containing numerous, small, PGE-bearing, related minerals found in placer deposits, which should zoned ultramafic complexes of the “Alaskan” or “Uralian” improve our understanding of their mineralogy, geochem­ type, or other related intrusive rocks. The even smaller PGE- istry, and genesis. bearing dunitic cores of these ultramafic complexes usually do not exceed about five square kilometers in area as cur­ rently exposed, e.g., Tagil [5.3 km2], Tulameen [5 km2], Analytical Techniques Joubdo [3.5 km2], Condoto [2 km2], and Omutnaya [1.7 km2]. The best examples of metallogenic belts associated The basic tool used for analysis of the PGE is the elec­ with rich PGE-bearing placers are the 1000 km-long belt in tron microprobe. Several different instruments were used northwestern Colombia and the 600 km-long belt in the over the twenty five-year period reported on in this paper. Urals, Russia. Published data on the recovery of PGE from The first data we collected were at the Mines Branch (now placer mining are few, and suffer imprecise mineralogical Canada Centre for Mineral and Energy Technology — information, as it is only in recent years that the PGM have CANMET) with a Materials Analysis Company (MAC) been better characterized. The principal PGM occurring in model 400 electron microprobe. Later, data were collected placers are the Pt-Fe and Os-Ir-Ru-Pt alloys, though other using a JEOL model 733 Superprobe at CANMET. At the liberated PGM are found occasionally. The PGM generally Geological Survey of Canada (GSC), a CAMECA occur as grains less than 1 millimetre in size, but larger Camebax, and, more recently, an SX-50 was employed. At grains and nuggets are also found. These alloys, especially the Federal Institute for Geosciences and Natural Resources the Pt-Fe alloys, often contain numerous inclusions of (BGR) of Germany, a Siemens ELMISONDE was used known and undefined PGM, as well as silicates, spinels, and originally, and, later, a CAMECA Camebax. In addition, dif­ base metal sulfides. The PGM alloys, in some cases, also ferent models of Scanning Electron Microscopes (SEM) show evidence of secondary PGM in the form of rims and were employed to characterize and image the PGM. cross-cutting veinlets. In general terms, the external mor­ Minerals were generally studied as polished sections, but phology and size of the PGM alloys is dependent on the dis­ were also mounted as SEM stubs to examine their morphol­ tance travelled. The largest grains, with well-preserved crys­ ogy and to provide qualitative analyses. tal faces, are usually found nearer the source rocks. As the instruments evolved, many different correction During the past 25 years, the authors have studied a programs were used to convert the X-ray intensities to con­ number of gold- and platinum-bearing placer deposits centrations. For example, the early computer program of worldwide, and published some of the results in scientific Rucklidge and Gasparrini (1969) was revised and updated journals (e.g., Cabri and Feather, 1975; Cabri and Harris, several times. However, well-characterized standards have 1975; Harris, 1974; Harris and Ballantyne, 1994; Harris and always been used, usually compounds synthesized from Cabri, 1991; Weiser and Schmidt-Thome, 1993). These pure elements. In addition, care was taken to correct any studies have resulted in the characterization of many new enhancements of primary X-ray lines by secondary lines of platinum-group mineral (PGM) species, in the redefinition other elements (see, for example, Crocket and Cabri, 1981). of other PGM species, and in the establishment of nomen­ The modem analysis of minor to trace elements using clature for some platinum-group element (PGE) systems microprobes is far superior compared to results from the (e.g., the Os-Ir-Ru-Pt alloys and the Pt-Fe alloys). This older instruments. We have not attempted to compare trace nomenclature (Cabri and Feather, 1975, and Harris and elements analysis from one laboratory to another using dif­ Cabri, 1991), which was approved by the Commission of ferent microprobes. New Minerals and Mineral Names of the International One of the major factors in trace element analysis is Mineralogical Association, is in use by the mineralogical the counting time. Because analytical routines were set up Mineralogy and Distribution of PGM Placer Deposits of the World * L.J. Cabri et al. 77 ° я* 15*- / - Alaska \ -■ I (1-14) Yukon “ч ;<ir ~ f'-jz-ST’: f :• nwt ' Л 1 ■ Finland 5 *(1)^ Г' f *oUrate —' , ‘1‘19> .. r- Alta . " ВС-A» (1Л2) Sasic, "'W fit, 1ЛЛ-Я'4^ . • (1-2| Great Britain^ ip \ * ?' ^Mongolia J‘Oregon ^'i,C^^Germany<l)-^i f/'''""' ' ^.Q4(1-2) Cоa-lвif)o rnia•^•O) (1-2t) _F( ria-гn)Sce о-ЗY-Sлw 'iVfee' r>ra wnd (t■)? * ~ /"f' Colombia •-"~ \ < *5 Ethiopia -_'L^ K {-^ .«M-r a7-l^aJ,ysia (1) Ecdua-3do) r /*: e; \ Л~ч 1 / ZairS*' >,/ '•••v6 4ч .\ «о ^r-^fXw RT • (1-2) 4 — ■ I(nмdoгneгsi'a- **^ <\•' D Madagascar ч O' -;4 V? 0B-r9az)il Y*o y'' " (1-4) - A(u1s-6tr)a lia % Ne(1w- 5C)aledonia South Africa •ii О / (1-6) 4 -о- mb Tasmania WORLDWIDE DISTRIBUTION d-в) С.- OF PGM PLACER DEPOSITS Fig. 1. Worldwide distribution of PGM placer deposits. The solid circles represent localities of worldwide PGM placer deposits examined by the authors, the open circles represent localities studied by other workers. The numbers represent the references listed in Appendix A. to analyze up to 20 elements on the same spot, the count­ In Table B.l of the Pt-Fe alloys, the p/f ratio represents ing time was usually limited to 10 or 20 seconds for each the atomic sum of the PGE (p) relative to the atomic sum of element in order to analyze the large number of grains Fe, Cu and Ni (f). This ratio was used to calculate the atom­ being studied. Most of the analyses plotted in the diagrams ic per cent (Fe,Cu,Ni) used in plotting the compositions of throughout this paper are mean values of several analyses, the Pt-Fe alloys. but where a large number of grains were analyzed, each More recently, Secondary Ion Mass Spectrometry point represents a single analysis. Unfortunately, it is not (SIMS) has been used to measure the 187Os/186Os ratios of practical to indicate whether a given point represents a sin­ osmium-bearing minerals occurring within PGM nuggets gle analysis or the average of several analyses. We realize and grains (Hattori et al., 1991, 1992; Hattori and Cabri, that not all the grains are homogeneous, but a study of 1992). Details of the analytical methodology for these in- homogeneity and zoning is best suited for a separate situ isotopic determinations are given by Hattori et al. SEM study. (1991). Determination of Os isotope ratios is based on the Microprobe analyses for all of the PGM that we have decay of 187Os (one of seven Os isotopes) to produce 187Re analyzed over the years are tabulated in Appendix B. with a half-life of 4.56 x 1010 years (Luck and Allegre, Although some of the data for the common Pt-Fe and Os-Ir- 1983). The 187Os/186Os of the bulk Earth was 0.805 at 4.55 Ru-Pt alloys and for many other PGM have been previous­ Ga, and the present value is approximately 1.04 (Allegre ly published (references are given), the majority are report­ and Luck, 1980). Because most Os resides in the mantle, the ed here for the first time. For most of the Pt-Fe and Os-Ir- values of the bulk Earth are close to the mantle values Ru-Pt alloys, results are presented in various types of dia­ (Allegre and Luck, 1980, Walker et al., 1989, 1991). On the grams, e.g., frequency diagrams showing the atomic per other hand, crustal rocks have high and varied Re/Os and cent (Fe,Cu,Ni) of the Pt-Fe alloys, and quaternary diagrams 1870s/1860s ratios, with an estimated average ratio of about illustrating compositions and mineral species of the Os-Ir- 30 (Palmer and Turekian, 1986, Palmer et al., 1988). As a Ru-Pt alloys. These diagrams are presented throughout the result of the large difference in 187Os/186Os ratios between text for the various localities discussed. For many of the mantle and crustal rocks, in-situ isotopic analysis of osmi­ accessory minerals where a large number of analyses exist, um-bearing minerals is a powerful method for determining ternary-quaternary diagrams are given to show their compo­ the source of the PGM in question, especially because sitional variations. For accessory minerals with a limited it is unbiased by subjective interpretation of textures number of analyses, the reader is referred to Appendix B. and geochemistry. 78 Explor. Mining Geol., Vol. 5, No. 2, 1996 Nomenclature of are imprecisely defined (Harris and Cabri, 1991). Analytical Platinum-group Element (PGE) Alloys results of natural Os-Ir-Ru-Pt alloys from our large database have enabled the boundaries in these alloy systems to be In 1992, the Nomenclature Subcommittee of the established more accurately. For example, recent data from ommission on New Minerals and Minerals Names the North Saskatchewan River, Edmonton, Alberta, permit (CNMMN) reviewed the naming of members of mineral refinement of the miscibility gap between rutheniridosmine solid-solution series. Earlier proposals for the nomenclature and iridium (Fig. 2). Because the miscibility gap probably of the Os-Ir-Ru-Pt system (Harris and Cabri, 1973) were narrows at higher temperatures, these data suggest that the used as a basis for discussions. The recommendations of the PGM originated from rocks that formed at slightly higher subcommittee,Approved by the CNMMN, were subsequent­ temperatures than those at which most such alloys formed. ly published in several journals by Nickel (1992). The Ultramafic rocks have not been found in Alberta, but recent nomenclature of alloys in the ternary systems Os-Ir-Ru, Os- exploration efforts have found kimberlitic rocks in the Peace Ir-Pt, Ru-Ir-Pt, Ir-Ru-Rh, Ir-Os-Rh and Pd-Ir-Pt has been River area, located some 400 km northwest of Edmonton. revised and reviewed by Harris and Cabri (1991). In Figure 2, the ternary systems Os-Ir-Ru and Ir-Os-Pt are illustrated, Nomenclature of Platinum-iron Alloys using the 50% rule for nomenclature currently approved by A nomenclature for the platinum-iron alloys, based on a the CNMMN. The minerals in the Os-Ir-Ru-Pt system are study of both natural and synthetic alloys, was published by either cubic (iridium and platinum) or hexagonal (osmium, Cabri and Feather (1975) following approval by the ruthenium and rutheniridosmine). CNMMN of the International Mineralogical Association. Synthesis work in the pure Os-Ir and Ru-Ir systems has The nomenclature allows for minor amounts of Ir, Pd, Rh, shown that a miscibility gap exists, although its boundaries Os, Ru that often substitute for Pt, and also minor amounts of Cu, Ni, Sb that substitute for Fe. In addition, the nomen­ clature discussed older names that are no longer acceptable Ru (e.g., “polyxene”, “ferroplatinum”), and also suggested an approved standard method for referring to alloys when only compositional data are available. The nomenclature for plat­ inum-iron alloys includes the following minerals: 1. Native platinum is defined to be a. face-centered cubic alloy with > 80 mol.% Pt. Ferroan platinum is defined as a variety of native platinum (Pt,Fe) with 20 to 50 mol.% Fe. 2. Isoferroplatinum is a primitive cubic alloy, with a composition usually near Pt3Fe, but with no precise compo­ sitional limits. 3. For Pt-Fe alloys with compositions in the range of 20 to 50 mol.% Fe, for which the crystal structure has not been determined, the mineral is referred to by the general name platinum-iron alloy or Pt-Fe alloy. 4. Tetraferroplatinum is a tetragonal alloy with a composition near PtFe, but for which the compositional lim­ its are not exactly defined. It should be noted that many Pt-Fe alloys in the litera­ ture with compositions close to Pt3Fe are erroneously called isoferroplatinum although lacking X-ray data which would support a primitive cubic structure. The difference between the two crystal structures can be seen on X-ray powder dif- fractograms through the absence or presence of a few weak reflections. It should be emphasized that the absence on a diffractogram of the weak reflections required by the primi­ tive cubic crystal structure of isoferroplatinum is not unequivocal proof of the mineral’s identity as ferroan plat­ inum. This is because of the poor diffracting properties of these alloys, which require confirmation of the structure by single crystal methods. Pt Mineralogy of Platinum-group Minerals (PGM) in Placer Deposits Fig. 2. The quaternary system Os-Ir-Ru-Pt and its nomenclature. The shaded areas represent slight modifications to the miscibility A listing of the mineral species reported in our studies gap proposed by Harris and Cabri (1991) because of new data.. of PGM placer deposits is given in Table 1. The most com- Mineralogy and Distribution of PGM Placer Deposits of the World • L.J. Cabri et al. 79 Table 1. Reported platinum-group minerals 1 | | | | | | | | 1 | 1 1 1 1 1 | 1 1 1 es ori Mineral Formula Australia, Tasmania Brazil, Itabira Burma, Chindwin River Canada, Alberta Canada, British Columbia Canada, North West Territ Canada, Saskatchewan Canada, Yukon Columbia, Choco Ecuador, Santiago River Ethiopia, Jourbdo Indonesia, Kalimantan Malaysia, Sabah Papua, New Guinea Russia, Urals Russia, West Chukot Sierra Leone South Africa Turkey, Ortakale River U.S., Alaska U.S., California I Arsenopalladinite Pds(As,Sb)3 • Atheneite (Pd,Hg)3As 0 Bowieite Rh2S3 0 0 0 0 0 0 Braggite (Pt,Pd,Ni)S 0 ф • 0 0 Cooperite PtS © 0 0 ® © 0 0 © Cuproiridsite CuIr2S4 0 © О Cuprorhodsite CuRh2S4 a © 0 0 0 0 Erlichmanite OSS2 0 0 © 0 0 0 • Ferronickelplatinum (Ni,Fe)Pt\ 0 " Genkinite (Pt,Pd)4Sb3 0 Geversite PtSb2 0 0 Hollingworthite RhAsS 0 0 0 ® 0 0 0 0 Hongshiite PtCu • 0 Irarsite IrAsS 0 © 0 0 ® 0 0 0 0 0 0 Iridarsenite IrAs2 \ 0 Iridium Ir © © • © • © © © • 0 • • • О Isoferroplatinum Pt3Fe • 0 © Isomertieite PdnSb2As2 © 0 Kashinite Ir2S3 0 © 0 0 О Keithconnite Pd3Te 0 0 Kotulskite PdTe 0 Laurite RuS2 © 0 0 © 0 0 © © 0 0 0 0 0 О Malanite CuPt2S4 0 0 0 0 Mertieite-II Pd8(Sb,As)3 О Osmium Os © 0 © © © © 0 0 0 0 © © • © 0 0 • • О Platarsite PtAsS 0 Platinum Pt • • • • • Pt-Fe alloy Pt-Fe 0 © © • © • • • • • • • 0 • • • © • • Rhodplumsite Rh3Pb2S2 0 Ruthenarsenite RuAs 0 Rutheniridosmine (Os,Ir,Ru) © © • © © • Ruthenium Ru © • • • • • 0 Sperry lite PtAs2 © • 0 • • © 0 • Stibiopalladinite Pd5Sb2 0 0 0 Tetraferroplatinum Pt Fe • 0 © • • Tolovkite IrSbS 0 0 Tulameenite Pt2FeCu © © © © • 0 0 Platinian Copper Cu,Pt 0 Gold Au • © • • • © © • • • © Rhodian Pentlandite (Fe,Ni,Rh)9S8 ® Rhodian Pyrrhotite (Fe,Rh)S 0 Undefined PGM 0 0 0 0 0 © 0 0 0 0 0 0 Undefined PGE-oxides 0 0 0 0 • Single grains © single grains and inclusions, exsolutions, etc. О inclusion, exsolution etc. © © probable 80 Explor. Mining Geol., Vol. 5, No. 2, 1996 mon species are the Os-Ir-Ru-Pt and the Pt-Fe alloys. In the tionally made possible the characterization of PGE oxides Os-Ir-Ru-Pt system, the species are osmium, ruthenium, and hydroxides alluded to in earlier studies (cf. Cabri et al., rutheniridosmine, iridium and rare platinum. The Pt-Fe sys­ 1981). Native gold, which can contain platinum-group ele­ tem is represented by platinum, isoferroplatinum (Pt3Fe) and ments in solid solution, is also common in PGM placers. tetraferroplatinum (PtFe). The identity of isoferroplatinum, Composite plots of the Os-Ir-Ru-Pt and Os-Ir-Rh-Pt though reported by other workers from several localities, is alloys which we have analyzed are shown in Figures 3 and doubtful without X-ray confirmation of the primitive cubic 4, together with their localities. In the second part of this structure. Tulameenite is often found as rims and replace­ paper, individual plots of alloys are presented for each local­ ments of other Pt-Fe alloys. ity, together with a brief site description. As illustrated in The P(jM alloys usually occur as discrete grains, and Figure 3, most of the Os-Ir-Ru-Pt alloys plot in the compo­ sometimes as intergrowths. The alloys invariably contain sitional field of hexagonal osmium, with fewer occurring as inclusions of many other PGM, as well as sulfides, silicates hexagonal ruthenium or hexagonal rutheniridosmine, or as and oxides. Some rater PGM inclusions include sperrylite, cubic iridium. Very few of these alloys contain platinum as hongshiite, arsenopalladinite, braggite, cooperite, mertieite- the third major element, when calculated as atomic per cent. II, tolovkite, bowieite, stibiopalladinite, rhodplumsite, Our overall data base shows an interesting trend from Os to hollingworthite, genkinite, kashinite, malanite, palladium, Ru for the hexagonal alloys which appears to follow the and also many unidentified species. Laurite, and to a lesser boundary of the miscibility gap. In contrast, the alloys that extent, erlichmanite, are common inclusions in Os-Ir-Ru-Pt plot in the field of cubic iridium, where iridium is the major alloys. Irarsite may occur either as idiomorphic crystals, or, element, are usually more platinum-rich and show no trend in many PGE alloys, as rims suggesting later replacement. lines. We have found three localities (Burma, Colombia and Chromite is the most common non-PGM inclusion, espe­ Urals) where some Os-Ir-Ru-Pt alloys contain Rh as the cially in the Pt-Fe alloys. Other non-PGM inclusions include third major element when calculated as atomic per cent. magnetite, olivine, pyroxenes, micas, and sulfides such as These localities are listed in Table B.10; the compositions, bornite, chalcopyrite, pentlandite, and cubanite. The recent which plot in the Os and Ir fields, are shown in Figure 4. capability of oxygen analysis using light-element detectors (e.g., Weiser, 1991; Legendre and Auge, 1993a) has addi­ ■ Australia, Tasmania Ethiopia о Brazil Indonesia о Burma Malaysia о Canada, Alberta Papua New Guinea a Canada, B.C. Russia, Urals © Canada, NWT Sierra Leone a Canada, Yukon Turkey л Colombia US, Alaska в Ecuador US, California Fig. 3. Composite plot of all Os-Ir-Ru-Pt alloys analyzed by the Fig. 4. Composite plot of all Os-Ir-Rh-Pt alloys analyzed by the authors, showing localities. authors, showing localities. Mineralogy and Distribution of PGM Placer Deposits of the World • L.J. Cabri et al. 81 Origin of PGM in Eluvial and Alluvial Placer temperature transport and deposition of Au-Pd-Pt grains in Deposits South Devon, England. However, there is a clear contrast Mertie (1969) discusses platinum placers in great detail, between the mineralogy of these grains (dendritic textures dividing them into seven different types (e.g., residual and elu­ and related zoning with no inclusions) and the PGM grains vial placers, stream placers, etc.). He concludes that placers and nuggets that we have studied. The latter nuggets show containing PGE are commonly derived from dunite or serpen- complex, sometimes oriented inclusions and intergrowths, tinite, in which the PGE are sparsely and irregularly distributed. as well as inclusions of minerals derived from the host pri­ In non-glaciated regions, the original lodes conceivably can be mary ultramafic rocks. A second example of nugget forma­ discovered by tracing the alluvial deposits upstream; however, tion in the surficial environment is provided by Cassedanne even though the country rock may be recognized, workable and Alves (1992), who report PGE nuggets in alluvial lodes are rarely located. Mertie (1969) also reports that plat­ deposits in central Minas Gerais, Brazil. These authors inum alloys (as well as gold) “rarely migrate far downstream describe “palladium-rich platinum nuggets” which have dis­ from their bedrock sources, unless they are so fine-grained as to tinct morphological features (reniform, mamillary, coral- be moved by swift water or floated by surface tension”. loidal, and dendritic) and which show no marks of abrasion. “Generally, however, ordinary detrital grains of platinum or Although the present paper does not discuss in detail gold work rapidly downward through alluvial deposits, and the origin of the PGM grains and nuggets that we have stud­ come to rest either near, on, or within bedrock”. Thus, except ied, it should be emphasized that textural, chemical, and for unusual situations (e.g., glaciation), “placers of the precious mineralogical evidence are all important to understanding metals may be assumed to lie within a few miles of their their genesis. One striking feature is the common presence bedrock sources” (Mertie, 1969). of intergrown non-PGM minerals in nuggets, especially of The origin of PGM in eluvial and alluvial placer deposits chromite. In some localities it has been shown that the became a controversial subject when Augustithis (1965) sug­ chemistry of the chromite, and of associated olivine inclu­ gested that “nuggets of native Pt formed in the lateritic soil” sions, matches with corresponding minerals in a nearby which capped the Joubdo ultramafic complex in Ethiopia, in dunite body, suggesting that the nuggets are detrital in ori­ contrast to the conclusions of many earlier studies (e.g., gin (cf., Nixon et al., 1990; Slansky et al., 1991). In addition, Duparc and Molly, 1928). This problem was critically exam­ the wide variety of PGM inclusions, some rare and exotic, ined by Cabri and Harris (1975), who discussed certain incon­ some occurring as very thin geometrically-oriented exsolu­ sistencies in interpretation of the data by Augustithis (1965). A tion lamellae or as droplet-shaped inclusions, and some as similar surficial genesis has been suggested by several authors idiomorphic crystals, all of which occur in the matrices of for a variety of deposits, including the PGM-bearing laterites Pt-Fe or Os-Ir-Ru-Pt alloys, can only be explained by a pri­ in Sierra Leone (e.g., Bowles, 1986, 1988) and the mary origin. For example, in Madagascar, the variety and Witwatersrand Au-U-PGM paleoplacers (e.g, Cousins, 1973). characteristics of PGM and silicate inclusions in Pt-Fe alloy Although the idea of surficial genesis was given impetus by nuggets indicate that they were originally formed in a mag- studies in theoretical and experimental PGE geochemistry, the matic environment (Legendre and Auge, 1992). results published to date are limited to compounds such as On the other hand, sedimented particles of quartz and pure Pt and Pd, which are quite unrelated to the diverse and layers of goethite, which are foreign to the source intrusive chemically complex PGM that occur in placers. Although it is rocks of placers, are sometimes associated with PGM clearly important to document the geochemical behavior of the nuggets, but clearly formed as late rims in the surficial envi­ PGE in solution, the mineralogy of PGE should also be con­ ronment, as indicated by their different texture and mineral- sidered in such geochemical studies. For example, it has been ogy (e.g., Cabri et al., 1981; Cabri and Genkin, 1991). The known for some time (as summarized in Cabri and Laflamme, larger size of PGE alloys that are found in placers, compared 1981) that sulfides and sulfarsenides contain trace amounts of to lode deposits, has often been cited as “proof’ that the PGE. Mineralogical studies suggest that PGE are dispersed nuggets grew in the placers (e.g., Cousins and Kinloch, 1976; through oxidation and dissolution of such minerals in the sur­ Bowles et al., 1994). However, Cabri and Genkin (1991) ficial environment, rather than by dissolution of PGM nuggets, have described a 10 mm-wide aggregate of tulameenite and which consist principally of PGE alloys. chromite in serpentine from a lode deposit in the Nizhni The complexly intergrown mineralogy and chemistry of Tagil dunite massif, Urals, and crystal aggregates of Pt-Fe many PGE grains and nuggets, their detailed mineralogical alloys greater than 13 mm in size have been found in the Pt- characteristics, and their correlation with host-rock petrolo­ rich dunite core of the Alto Condoto zoned ultramafic com­ gy, all argue for a primary source for PGE grains and plex in Colombia (Salinas et al., 1992; Salinas and Tistl, nuggets. Such evidence is not discussed by those postulating 1991). Unfortunately, rich lode deposits, such as at Krutoy formation of PGE grains and nuggets in the surficial envi­ Log (Mertie, 1969), were all exploited in the past, and little ronment (e.g., Bowles, 1986, 1988; Cousins 1973), who textural or mineralogical data are now available. However, it describe only the morphology of the nuggets. An apparent was known by the early workers that rich PGE accumula­ exception is the study of Leake et al. (1991), the first exam­ tions did occur within ultramafic rocks, although they were ple to our knowledge to show clear evidence of formation of few in number and were widely separated in the host intru­ PGE alloys in the surficial environment. Leake et al. (1991) sions (Mertie, 1969). Therefore, such primary deposits were documented textural and chemical evidence for low- difficult to find, as is also reported to be the case in recent 82 Explor. Mining Geol., Vol. 5, No. 2, 1996 studies (e.g., Tistl, 1994). Clearly, the evidence for primary Canada mineralization generally has been removed by the erosion of Yukon: Florence Creek enormous quantities of source rocks. Source of sample: The Florence Creek PGM weri One fruitful approach to understanding the origin of obtained from a Au-Pt-bearing heavy mineral concentrate PGM grains and nuggets is through in-situ measurements of that was donated by Bob Wonga of Whitehorse, Yukor certain isotope ratios, as first documented by Hattori et al. Territory. Twelve grains ranging from 1.8 x 1.4 mm to 30( (1991, 1992) and Hattori and Cabri (1992). The first study x 700 цт were recovered from the concentrate (Ballantynt showed that erlichmanite nuggets from Sierra Leone have and Harris, 1991). ,S7Os/1S6Os ratios comparable with mantle values, whereas Geological setting: Locally, the area is underlain b) Pt-Fe nuggets had slightly higher ratios. Although the data hornblende granodiorite and porphyritic quartz monzonite forthe Pt-Fe nuggets suggest that some later geochemical granitoid rocks. Regional aeromagnetic data do not reveal contamination occurred, the ratios are still more than ten strong magnetic features, which are often characteristic ol times less than those of the continental crust and black ultramafic-mafic rocks. shales. In the study by Hattori and Cabri (1992), Os-isotope Description of PGM and related minerals: ratios were determined in osmium and osmium-bearing Microprobe analyses show that all grains are Pt-Fe alloys PGM for samples from worldwide placers associated with with some close to PtFe in composition (Fig. 5, Table B.l). five Alaskan-type ultramafic complexes (Tulameen in 3 Recent X-ray powder diffraction data for a Pt-Fe alloy grain British Columbia, Choco in Colombia, Nizhni Tagil and with 24-25 at. % (Fe, Cu, Ni) indicate a disordered face-cen­ Omutnaya in Russia, Joubdo in Ethiopia, and Goodnews tred cubic mineral (i.e., ferroan platinum), not isoferroplat­ Bay in Alaska) and with five Alpine-type intrusions (Atlin, inum as reported earlier (Ballantyne and Harris, 1991). One Ruby Creek, and Cariboo in British Columbia, Adamsfield ferroan platinum grain contained four drop-like sulfide inclu­ in Tasmania, Teshio and Onnebetsu in Japan, and in sions of bomite-digenite (50 |лт diameter), which in turn Borneo). All PGM analyzed from all localities had isotopic host inclusions of (Pt,Pd)S (braggite?) and an undefined Pt- ratios consistent with the mantle 1870s/1860s value. This remarkable result fully supports existing mineralogical and petrological evidence that PGE mineralization initially formed within ultramafic intrusive rocks, but subsequently Ш Florence Creek was concentrated mechanically in placers as grains and nuggets through weathering. In summary, most modem mineralogical and petrologi­ cal studies of PGE-bearing grains and nuggets from world­ wide sources have confirmed that the origin of PGM is due to high-temperature mineralization related to mafic and ultra­ mafic intrusions, including the following areas: Colombia \ \ (Salinas et al., 1992, Tistl, 1994), Fifield, Australia (Johan et al., 1991a, 1991b, Slansky et al., 1991), Tulameen, Canada 1 i 1 1 1 i l 1 1 l 1 1 ■ 1 1 1 1 1 1 r 1 1 r (Nixon et al., 1989, 1990), Indonesia (Zientek et al., 1992), io ti 12 13 и ie 16 it ie 10 20 212223242620272820303132 33Э4Э8 AL % (Fe.Cu.NI) and Madagascar (Legendre and Auge, 1992). This interpre­ (Bu»d on total 4 atom*) tation is supported by Os isotopic studies which have con­ Fig. 5. Frequency diagram showing at.% (Fe,Cu,Ni) contents of Pt- firmed that placer platinum-group minerals consistently have Fe alloys from Florence Creek, Yukon. 187Os/186Os ratios within the range of accepted mantle signa­ tures (Hattori et al., 1992; Hattori and Cabri, 1992). Descriptions of Individual PGM Placer Deposits The following section of the paper contains chemical data and brief descriptions of placer deposits which we have studied. In a few cases we were involved in sample collec­ tion and investigations of the placers. Generally, however, samples were obtained directly from collections or through colleagues. The mineral abundances cited below therefore may be biased either by sample collection or by methods of concentration of the rare PGM. This is especially important when making comparisons with bulk geochemical data, which, ideally, should be determined only on the basis of mining operations over many years (cf. Mertie, 1976). The Fig. 6. Backscattered electron image (BEI) of a Pt-Fe alloy with an descriptions given below are accompanied by analytical inclusion of bomite and digenite that contains inclusions of data, figures, and photomicrographs of nuggets and PGM Pt,Pd,Cu,S (braggite?) and an undefined Pt-Rh-S from Florence (both unpublished and previously published). Creek, Yukon.

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