Disseminated ores in the Norilsk 1 intrusion were studied to elucidate the typomorphic features of sulfides and noble metal mineralizations in picritic and taxitic (or lower olivine) gabbro-dolerites. The former are characterized by the development of a low-sulfur sulfide association (troilite, Fe-rich pentlandite, talnakhite, chalcocite, native copper) while the latter exhibits a high-sulfur association (monoclinic pyrrhotite, Ni-rich pentlandite, pyrite, heazlewoodite). The contact between these types of rocks is geochemically and mineralogically contrasting. The mineralogical and geochemical zoning directed from the roof to the base of each layer is expressed by an increase in the Cu content (and chalcopyrite) in ores, an increase in the concentration of Ni in pentlandite and S in pyrrhotite in line with a decrease of the crystallization temperature, and an increase in sulfur fugacity in the same direction. Zoning of Pd(Pt) mineralization in picritic and taxitic (olivine) gabbro-dolerites is uniform and characterized by the distribution of Pd-Sn compounds in the upper parts (together with Pd-Pb minerals in picritic rocks) and Pd-As compounds in the lower parts of the sections according to a drop in temperature. Such reverse zoning contradicts the typical mechanism of differentiation by fractional crystallization, and possibly suggests a fluid-magmatic nature. Mineralogical and geochemical features in platinum group element-Cu-Ni-bearing rocks are consistent with the idea that different stages of multi-pulse intrusions of mafic-ultramafic magmas with different compositions formed the picritic and taxitic gabbro-dolerites of the Norilsk region.
研究了诺里尔斯克1岩体中的浸染状矿石，阐明了苦橄辉长榴辉岩和滑石(或下橄榄石)辉长榴辉岩中硫化物和贵金属矿化的标型特征。前者主要发育低硫硫化物组合(三黄铁矿、富铁镍黄铁矿、滑石、辉铜矿、原生铜)，后者主要发育高硫组合(单斜磁黄铁矿、富镍镍镍黄铁矿、黄铁矿、黄铁矿)。这些岩石类型之间的接触在地球化学和矿物学上形成对比。矿石中铜(和黄铜矿)含量随结晶温度的降低而增加，镍(硫铁矿)和硫(磁黄铁矿)的含量随结晶温度的降低而增加，硫逸度随结晶温度的降低而增加，矿物地球化学和地球化学的分带性也随结晶温度的降低而增加。苦橄岩和橄榄石辉长白云岩中Pd(Pt)矿化分带均匀，其特征为:Pd- sn化合物(与苦橄岩中的Pd- pb矿物一起)在剖面上部分布，Pd- as化合物在剖面下部按温度递减分布。这种反向分带与典型的分异结晶分异机制相矛盾，可能显示出流体-岩浆的性质。铂族元素- cu - ni含岩的矿物学和地球化学特征与诺里尔斯克地区不同组成的基性-超基性岩浆多脉冲侵入的不同阶段形成了辉长岩和滑石辉长岩的观点一致。
{"title":"Distribution of sulfides and PGE minerals in the picritic and taxitic gabbro-dolerites of the Norilsk 1 intrusion","authors":"N. Tolstykh, J. García, G. Shvedov","doi":"10.3749/canmin.2100037","DOIUrl":"https://doi.org/10.3749/canmin.2100037","url":null,"abstract":"\u0000 Disseminated ores in the Norilsk 1 intrusion were studied to elucidate the typomorphic features of sulfides and noble metal mineralizations in picritic and taxitic (or lower olivine) gabbro-dolerites. The former are characterized by the development of a low-sulfur sulfide association (troilite, Fe-rich pentlandite, talnakhite, chalcocite, native copper) while the latter exhibits a high-sulfur association (monoclinic pyrrhotite, Ni-rich pentlandite, pyrite, heazlewoodite). The contact between these types of rocks is geochemically and mineralogically contrasting. The mineralogical and geochemical zoning directed from the roof to the base of each layer is expressed by an increase in the Cu content (and chalcopyrite) in ores, an increase in the concentration of Ni in pentlandite and S in pyrrhotite in line with a decrease of the crystallization temperature, and an increase in sulfur fugacity in the same direction. Zoning of Pd(Pt) mineralization in picritic and taxitic (olivine) gabbro-dolerites is uniform and characterized by the distribution of Pd-Sn compounds in the upper parts (together with Pd-Pb minerals in picritic rocks) and Pd-As compounds in the lower parts of the sections according to a drop in temperature. Such reverse zoning contradicts the typical mechanism of differentiation by fractional crystallization, and possibly suggests a fluid-magmatic nature. Mineralogical and geochemical features in platinum group element-Cu-Ni-bearing rocks are consistent with the idea that different stages of multi-pulse intrusions of mafic-ultramafic magmas with different compositions formed the picritic and taxitic gabbro-dolerites of the Norilsk region.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132681027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. Oberthür, F. Melcher, S. Goldmann, Fabian Fröhlich
The platiniferous dunite pipes are discordant orebodies in the Bushveld Complex. The Onverwacht pipe is a large body (>300 m in diameter) of magnesian dunite (Fo80–83) that crosscuts a sequence of cumulates in the Lower Critical Zone of the Bushveld Complex. In a pipe-in-pipe configuration, the main dunite pipe at Onverwacht hosts a carrot-shaped inner pipe of Fe-rich dunite pegmatite (Fo46–62) which comprises the platinum-bearing orebody. The latter was ca. 18 m in diameter and a mining depth of about 320 m was reached. In the present work, a variety of ore samples were studied by whole-rock geochemistry, including analyses of platinum group elements, ore microscopy, and electron probe microanalysis. Olivine of the ore zone displays considerable chemical variation (range 46–62 mol.% Fo) and may represent either a continuum, or different batches of magma, or vertical or horizontal zonation within the ore zone. Chromite is principally regarded to be a consanguineous component of the pipe magma that crystallized in situ and simultaneously with olivine. The Onverwacht mineralization is Pt-dominated (>95% of the platinum group elements) and the ore is virtually devoid of sulfides. Platinum-dominated platinum group minerals predominate, followed by Rh-, Pd-, and Ru-species. Pt-Fe alloys are most frequent, followed by Pt-Rh-Ru-arsenides and -sulfarsenides, platinum group element antimonides, and platinum group element sulfides. Our hypothesis on the genesis of the Onverwacht pipe and its mineralization is as follows: After near-consolidation of the layered series of the Critical Zone, the magnesian dunite pipe of Onverwacht was formed by upward penetration of magmas that replaced the existing cumulates initially by infiltration, followed by the development of a central channel where large volumes of magma flowed through. Fractional crystallization of olivine within the deeper magma chamber and/or during ascent of the melt resulted in the formation of a consanguineous, residual, more iron-rich melt. This melt also contained highly mobile, supercritical, water-bearing fluids and was continuously enriched in platinum group elements and other incompatible elements. In several closing pulses, the platinum group element-enriched residual melts crystallized and sealed the inner ore pipe. Crystallization of the melt resulted in the coeval formation of Fe-rich olivine, chromite, and platinum group minerals. The non-sulfide platinum group element mineralization was introduced in the form of nanoparticles and small droplets of platinum group minerals, which coagulated to form larger grains during evolution of the mineralizing system. The suspended platinum group minerals acted as collectors of other platinum group elements and incompatible elements during generation and ascent of the melt. With decreasing temperature, the platinum group mineral grains annealed and recrystallized, leading to the formation of composite platinum group mineral grains, complex in
{"title":"High grade ores of the Onverwacht platinum pipe, eastern Bushveld, South Africa","authors":"T. Oberthür, F. Melcher, S. Goldmann, Fabian Fröhlich","doi":"10.3749/canmin.2100031","DOIUrl":"https://doi.org/10.3749/canmin.2100031","url":null,"abstract":"\u0000 The platiniferous dunite pipes are discordant orebodies in the Bushveld Complex. The Onverwacht pipe is a large body (>300 m in diameter) of magnesian dunite (Fo80–83) that crosscuts a sequence of cumulates in the Lower Critical Zone of the Bushveld Complex. In a pipe-in-pipe configuration, the main dunite pipe at Onverwacht hosts a carrot-shaped inner pipe of Fe-rich dunite pegmatite (Fo46–62) which comprises the platinum-bearing orebody. The latter was ca. 18 m in diameter and a mining depth of about 320 m was reached.\u0000 In the present work, a variety of ore samples were studied by whole-rock geochemistry, including analyses of platinum group elements, ore microscopy, and electron probe microanalysis.\u0000 Olivine of the ore zone displays considerable chemical variation (range 46–62 mol.% Fo) and may represent either a continuum, or different batches of magma, or vertical or horizontal zonation within the ore zone. Chromite is principally regarded to be a consanguineous component of the pipe magma that crystallized in situ and simultaneously with olivine. The Onverwacht mineralization is Pt-dominated (>95% of the platinum group elements) and the ore is virtually devoid of sulfides. Platinum-dominated platinum group minerals predominate, followed by Rh-, Pd-, and Ru-species. Pt-Fe alloys are most frequent, followed by Pt-Rh-Ru-arsenides and -sulfarsenides, platinum group element antimonides, and platinum group element sulfides.\u0000 Our hypothesis on the genesis of the Onverwacht pipe and its mineralization is as follows: After near-consolidation of the layered series of the Critical Zone, the magnesian dunite pipe of Onverwacht was formed by upward penetration of magmas that replaced the existing cumulates initially by infiltration, followed by the development of a central channel where large volumes of magma flowed through. Fractional crystallization of olivine within the deeper magma chamber and/or during ascent of the melt resulted in the formation of a consanguineous, residual, more iron-rich melt. This melt also contained highly mobile, supercritical, water-bearing fluids and was continuously enriched in platinum group elements and other incompatible elements. In several closing pulses, the platinum group element-enriched residual melts crystallized and sealed the inner ore pipe. Crystallization of the melt resulted in the coeval formation of Fe-rich olivine, chromite, and platinum group minerals. The non-sulfide platinum group element mineralization was introduced in the form of nanoparticles and small droplets of platinum group minerals, which coagulated to form larger grains during evolution of the mineralizing system. The suspended platinum group minerals acted as collectors of other platinum group elements and incompatible elements during generation and ascent of the melt. With decreasing temperature, the platinum group mineral grains annealed and recrystallized, leading to the formation of composite platinum group mineral grains, complex in","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133031346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yiguan Lu, C. Lesher, Li‐Qiang Yang, M. Leybourne, Wen-yan He
The ∼259 Ma Baimazhai Ni-Cu-(platinum-group element) deposit is located in the Ailaoshan-Red River fault zone on the southwest margin of the Yangtze Plate in the Jinping area of southeastern Yunnan Province. The intrusion is lenticular (∼530 m long × 190 m wide × 24–64 m thick) and concentrically zoned (margin to core) from gabbro through pyroxenite to peridotite. It contains ∼50 kt of Ni-Cu-(platinum-group element) mineralization, concentrically zoned (margin to core) from disseminated through net-textured to massive sulfides with an average grade of 1.03 wt.% Ni, 0.81 wt.% Cu, and 0.02∼0.69 ppm Pd+Pt. The sulfide assemblage comprises pyrrhotite, chalcopyrite, and pentlandite, with lesser magnetite, violarite, galena, and cobaltite. The mineralization is enriched in Ni-Cu-Co relative to the platinum-group elements and the host rocks are enriched in highly incompatible lithophile elements relative to moderately incompatible lithophile elements with high Th/Yb and intermediate Nb/Yb ratios. These host rocks, and those at most other Ni-Cu-platinum-group element deposits in the Emeishan Large Igneous Province, have high γOs and intermediate εNd values, indicating that they crystallized from a magma derived from a subduction-modified pyroxenite mantle source and modified by crustal contamination. The initial concentrations of metals in the primary magma are estimated to have been on the order of 200 ppm Ni and 100 ppm Cu, but only 0.4 ppb Pd, 0.2 ppb Pt, 0.005 ppb Rh, 0.02 ppb Ru, and 0.01 ppb Ir. The δ34S values of ores and separated sulfides range from 5.8‰ to 8.6‰, between the ∼10‰ value of sulfides in the metasedimentary country rocks and the 0 ± 0.5‰ value expected for magmas derived from MORB-type mantle, or the –2.5 ± 0.3‰ value expected for subduction-modified mantle, consistent with equilibration at magma:sulfide mass ratios (R factors) of 100–1000. Variations in Ir100 and Pd100 (metals in 100% sulfide) are consistent with 40–60% fractional crystallization of monosulfide solid solution to form Ni-Co-intermediate platinum-group element (Ru, Os, Ir)-rich massive ores and Cu-palladium/platinum-group elements (Pt, Pd, Rh)-Au-rich residual sulfide liquids. This process is also recorded by magnetite: Type I (early magmatic), type II (late magmatic), and type III (secondary) magnetites exhibit progressively lower Cr-Ti-V concentrations. The platinum-group element contents in base-metal minerals are low, and only pentlandite, violarite, and cobaltite contain detectable concentrations of Pd, Rh, and Ru. There is abundant textural evidence for metamorphic-hydrothermal alteration of sulfides in the Baimazhai intrusion, with secondary violarite, chalcopyrite, and pentlandite being enriched (Ag, Sb, Au, Pb) or depleted (Sn) in more mobile chalcophile elements. The different tectonic and petrogenetic settings of the Baimazhai and other deposits in China highlight the potential of Ni-Cu-platinum-group element deposits to occur in subduction or post-subdu
{"title":"Genesis and mechanisms of metal enrichment in the Baimazhai Ni-Cu-(PGE) deposit, Ailaoshan Orogenic Belt, SW China","authors":"Yiguan Lu, C. Lesher, Li‐Qiang Yang, M. Leybourne, Wen-yan He","doi":"10.3749/canmin.2100057","DOIUrl":"https://doi.org/10.3749/canmin.2100057","url":null,"abstract":"\u0000 The ∼259 Ma Baimazhai Ni-Cu-(platinum-group element) deposit is located in the Ailaoshan-Red River fault zone on the southwest margin of the Yangtze Plate in the Jinping area of southeastern Yunnan Province. The intrusion is lenticular (∼530 m long × 190 m wide × 24–64 m thick) and concentrically zoned (margin to core) from gabbro through pyroxenite to peridotite. It contains ∼50 kt of Ni-Cu-(platinum-group element) mineralization, concentrically zoned (margin to core) from disseminated through net-textured to massive sulfides with an average grade of 1.03 wt.% Ni, 0.81 wt.% Cu, and 0.02∼0.69 ppm Pd+Pt. The sulfide assemblage comprises pyrrhotite, chalcopyrite, and pentlandite, with lesser magnetite, violarite, galena, and cobaltite. The mineralization is enriched in Ni-Cu-Co relative to the platinum-group elements and the host rocks are enriched in highly incompatible lithophile elements relative to moderately incompatible lithophile elements with high Th/Yb and intermediate Nb/Yb ratios. These host rocks, and those at most other Ni-Cu-platinum-group element deposits in the Emeishan Large Igneous Province, have high γOs and intermediate εNd values, indicating that they crystallized from a magma derived from a subduction-modified pyroxenite mantle source and modified by crustal contamination. The initial concentrations of metals in the primary magma are estimated to have been on the order of 200 ppm Ni and 100 ppm Cu, but only 0.4 ppb Pd, 0.2 ppb Pt, 0.005 ppb Rh, 0.02 ppb Ru, and 0.01 ppb Ir. The δ34S values of ores and separated sulfides range from 5.8‰ to 8.6‰, between the ∼10‰ value of sulfides in the metasedimentary country rocks and the 0 ± 0.5‰ value expected for magmas derived from MORB-type mantle, or the –2.5 ± 0.3‰ value expected for subduction-modified mantle, consistent with equilibration at magma:sulfide mass ratios (R factors) of 100–1000. Variations in Ir100 and Pd100 (metals in 100% sulfide) are consistent with 40–60% fractional crystallization of monosulfide solid solution to form Ni-Co-intermediate platinum-group element (Ru, Os, Ir)-rich massive ores and Cu-palladium/platinum-group elements (Pt, Pd, Rh)-Au-rich residual sulfide liquids. This process is also recorded by magnetite: Type I (early magmatic), type II (late magmatic), and type III (secondary) magnetites exhibit progressively lower Cr-Ti-V concentrations. The platinum-group element contents in base-metal minerals are low, and only pentlandite, violarite, and cobaltite contain detectable concentrations of Pd, Rh, and Ru. There is abundant textural evidence for metamorphic-hydrothermal alteration of sulfides in the Baimazhai intrusion, with secondary violarite, chalcopyrite, and pentlandite being enriched (Ag, Sb, Au, Pb) or depleted (Sn) in more mobile chalcophile elements. The different tectonic and petrogenetic settings of the Baimazhai and other deposits in China highlight the potential of Ni-Cu-platinum-group element deposits to occur in subduction or post-subdu","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116124750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Chistyakova, R. Latypov, F. Kruger, F. Zaccarini
The Upper Zone of the Bushveld Complex has long been known to have formed from a major influx of magma into the chamber that caused large-scale erosion of the chamber floor cumulates. The most dramatic manifestations of this process are two major gap areas (Northern and Southern) in the western Bushveld Complex in which the Upper Zone appears to have eroded away the underlying cumulates down to the very base of the Complex. However, due to almost complete lack of outcrops in the gap areas, no direct field observations have ever been reported to confirm the transgressive nature of the Upper Zone. Here, we present for the first time such observations from the Kameelhoek chromite mine located at the margin of the Northern Gap. In the open pit we have documented several transgressive depressions (up to 40 m in width) in the orthopyroxenite and chromitites of the Lower Critical Zone that are filled in with magnetite gabbro of the Upper Zone. The magnetite gabbro is chilled against the sidewalls of the depressions, forming glassy and fine-grained textured rocks with plagioclase laths arranged in radial clusters. Mineralogically and chemically, the magnetite gabbro correlates with cumulates from the lowermost part of the Upper Zone at its normal position in the complex. Three major points that have emerged from this study are: (1) the Critical Zone has been eroded away by magma that was parental to the Upper Zone, (2) this eroding magma was not the one that initiated formation of the Pyroxenite Marker, but rather the evolved melt that replenished the chamber at some later stage, and (3) the melt was phenocryst-free and likely derived from a deep-seated staging chamber. Our study thus supports a recent notion that even during the formation of the Upper Zone, the Bushveld chamber had still been operating as an open system that was replenished by melts from deeper magma sources.
{"title":"Transgressive nature and chilled margins of the Upper Zone in the western Bushveld Complex, South Africa","authors":"S. Chistyakova, R. Latypov, F. Kruger, F. Zaccarini","doi":"10.3749/canmin.2100027","DOIUrl":"https://doi.org/10.3749/canmin.2100027","url":null,"abstract":"\u0000 The Upper Zone of the Bushveld Complex has long been known to have formed from a major influx of magma into the chamber that caused large-scale erosion of the chamber floor cumulates. The most dramatic manifestations of this process are two major gap areas (Northern and Southern) in the western Bushveld Complex in which the Upper Zone appears to have eroded away the underlying cumulates down to the very base of the Complex. However, due to almost complete lack of outcrops in the gap areas, no direct field observations have ever been reported to confirm the transgressive nature of the Upper Zone. Here, we present for the first time such observations from the Kameelhoek chromite mine located at the margin of the Northern Gap. In the open pit we have documented several transgressive depressions (up to 40 m in width) in the orthopyroxenite and chromitites of the Lower Critical Zone that are filled in with magnetite gabbro of the Upper Zone. The magnetite gabbro is chilled against the sidewalls of the depressions, forming glassy and fine-grained textured rocks with plagioclase laths arranged in radial clusters. Mineralogically and chemically, the magnetite gabbro correlates with cumulates from the lowermost part of the Upper Zone at its normal position in the complex. Three major points that have emerged from this study are: (1) the Critical Zone has been eroded away by magma that was parental to the Upper Zone, (2) this eroding magma was not the one that initiated formation of the Pyroxenite Marker, but rather the evolved melt that replenished the chamber at some later stage, and (3) the melt was phenocryst-free and likely derived from a deep-seated staging chamber. Our study thus supports a recent notion that even during the formation of the Upper Zone, the Bushveld chamber had still been operating as an open system that was replenished by melts from deeper magma sources.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"52 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115123647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. McDonald, D. Ames, I. Kjarsgaard, L. Cabri, William Zhe, K. C. Ross, D. Good
Marathonite, Pd25Ge9, and palladogermanide, Pd2Ge, are two new platinum-group minerals discovered in the Marathon deposit, Coldwell Complex, Ontario, Canada. Marathonite is trigonal, space group P3, with a 7.391(1), c 10.477(2) Å, V 495.6(1) Å3, Z = 1. The six strongest lines of the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.436(10)(014,104,120,210), 2.374(29)(023,203,121,211), 2.148(100)(114,030), 1.759(10)(025,205,131,311), 1.3605(13)(233,323,036,306), and 1.2395(14)(144,414,330). Associated minerals include: vysotskite, Au-Ag alloy, isoferroplatinum, Ge-bearing keithconnite, majakite, coldwellite, ferhodsite-series minerals (cuprorhodsite-ferhodsite), kotulskite and mertieite-II, the base-metal sulfides, chalcopyrite, bornite, millerite and Rh-bearing pentlandite, oberthürite and torryweiserite, and silicates including a clinoamphibole and a Fe-rich chlorite-group mineral. Rounded, elongated grains of marathonite are up to 33 × 48 μm. Marathonite is white, but pinkish brown compared to palladogermanide and bornite. No streak or microhardness could be measured. The mineral shows no discernible pleochroism, bireflectance, or anisotropy. The reflectance values (%) in air for the standard COM wavelengths are: 40.8 (470 nm), 44.1 (546 nm), 45.3 (589 nm), and 47.4 (650 nm). The calculated density is 10.933 g/cm3, determined using the empirical formula and the unit-cell parameters from the refined crystal structure. The average result (n = 19) using energy-dispersive spectrometry is: Si 0.11, S 0.39, Cu 2.32, Ge 18.46, Pd 77.83, Pt 1.10, total 100.22 wt.%, corresponding to the empirical formula (based on 34 apfu): (Pd23.82Cu1.19Pt0.18)Σ25.19(Ge8.28S0.40Si0.13)∑8.81 and the simplified formula is Pd25Ge9. The name is for the town of Marathon, Ontario, Canada, after which the Marathon deposit (Coldwell complex) is named. Results from electron backscattered diffraction show that palladogermanide is isostructural with synthetic Pd2Ge. Based on this, palladogermanide is considered to be hexagonal, space group , with a 6.712(1), c 3.408(1) Å, V 133.0(1), Z = 3. The seven strongest lines of the X-ray powder-diffraction pattern calculated for the synthetic analogue [d in Å (I)(hkl)] are: 2.392(100)(111), 2.211(58)(201), 2.197(43)(210), 1.937(34)(300), 1.846(16)(211), 1.7037(16)(002), and 1.2418(18)(321). Associated minerals are the same as for marathonite. Palladogermanide occurs as an angular, anhedral grain measuring 29 × 35 μm. It is white, but grayish-white when compared to marathonite, bornite, and chalcopyrite. Compared to zvyagintsevite, palladogermanide is a dull gray. No streak or microhardness could be measured. The mineral shows no discernible pleochroism, bireflectance, or anisotropy. The reflectance values (%) in air for the standard COM wavelengths for Ro and Ro' are: 46.8, 53.4 (470 nm), 49.5, 55.4 (546 nm), 50.1, 55.7 (589 nm), and 51.2, 56.5 (650 nm). The calculated density is 10.74 g/cm3, determined using the empirical form
Marathon onite (Pd25Ge9)和palladogermanide (Pd2Ge)是在加拿大安大略省Coldwell杂岩Marathon矿床中发现的两种新铂族矿物。马拉松石为三角形，空间群为P3，具有a = 7.391(1)， c = 10.477(2) Å， V = 495.6(1) Å3, Z = 1。x射线粉末衍射图的六个最强谱线[d在Å (I)(hkl)中]是:2.436(10)(014,104,120,210)，2.374(29)(023,203,121,211)，2.148(100)(114,030)，1.759(10)(025,205,131,311)，1.3605(13)(233,323,036,306)和1.2395(14)(144,414,330)。伴生矿物包括:钒钙钛矿、金银合金、异铁铂、含锗钾辉石、镁辉石、铁长石、铁长石系列矿物(铜长石-铁长石)、钾长石和银长石ii、贱金属硫化物、黄铜矿、斑铜矿、针长石和含铑镍长石、黄铜矿和托利辉长石，以及包括斜角闪孔和富铁绿泥石群矿物在内的硅酸盐。马拉脱石晶粒尺寸为33 × 48 μm，呈圆形、细长状。马拉脱石是白色的，但与帕拉戈马尼特和斑铜矿相比是粉棕色的。无法测量条纹或显微硬度。这种矿物没有明显的多色性、双反射性或各向异性。标准COM波长在空气中的反射率值(%)分别为:40.8 (470 nm)、44.1 (546 nm)、45.3 (589 nm)和47.4 (650 nm)。利用经验公式和精细化晶体结构的单胞参数计算得到的密度为10.933 g/cm3。能量色散光谱平均结果(n = 19)为:Si 0.11, S 0.39, Cu 2.32, Ge 18.46, Pd 77.83, Pt 1.10，总计100.22 wt.%，对应经验公式(基于34 apfu):(Pd23.82Cu1.19Pt0.18)Σ25.19(Ge8.28S0.40Si0.13)∑8.81，简化公式为Pd25Ge9。这个名字是加拿大安大略省马拉松镇的名字，马拉松矿床(Coldwell complex)就是以它命名的。电子背散射衍射结果表明，钯锗酰胺与合成的Pd2Ge呈同构关系。在此基础上，认为钯锗酰胺为六边形，空间群，具有a = 6.712(1)， c = 3.408(1) Å， V = 133.0(1)， Z = 3。合成类似物[Å (I)(hkl)]的x射线粉末衍射图的7条最强谱线为:2.392(100)(111)、2.211(58)(201)、2.197(43)(210)、1.937(34)(300)、1.846(16)(211)、1.7037(16)(002)和1.2418(18)(321)。伴生矿物与马拉松石相同。palladogmanide以棱角分明、大小为29 × 35 μm的四面体晶粒形式出现。它是白色的，但与马拉松矿、斑铜矿和黄铜矿相比是灰白色的。与zvyagintsevite相比，palladogermanide呈暗灰色。无法测量条纹或显微硬度。这种矿物没有明显的多色性、双反射性或各向异性。Ro和Ro′的标准COM波长在空气中的反射率值(%)分别为:46.8、53.4 (470 nm)、49.5、55.4 (546 nm)、50.1、55.7 (589 nm)和51.2、56.5 (650 nm)。计算密度为10.74 g/cm3，由经验公式和合成Pd2Ge的单胞参数确定。波长色散光谱的平均结果(n = 14)为:Si 0.04, Fe 0.14, Cu 0.06, Ge 25.21, Te 0.30, Pd 73.10, Pt 0.95, Pb 0.08，总计99.88 wt.%，对应(基于3 apfu)为:(Pd1.97Pt0.01Fe0.01)Σ1.99(Ge1.00Te0.01)∑1.01，理想情况下为Pd2Ge。这个名字来源于它的化学性质以及它与钯硅化物的关系。用x射线单晶衍射法解析了马拉松石的晶体结构(R = 7.55, wR2 = 19.96%)。它基于两个基本模块，一个有序，一个无序，沿[001]交替。有序模块，厚度约7.6 Å，基于一个简单的Pd4Ge3单元，由Pd原子交联形成一个六元三角环，从而产生一个层状模块，包含完全占据的Pd和Ge位点。这沿着[001]与高度无序的模块交替，厚度为~ 3 Å，由许多部分占据的Pd和Ge位点组成。将有序模块和无序模块中的位点组合得到Pd25Ge9的化学计量公式。共成序为:斑岩→马拉脱石→帕拉多格曼尼。Pd-Ge体系的相平衡研究表明，Pd25Ge9(马拉松石)在550-970°C范围内稳定，Pd2Ge(钯锗酰胺)在200°C范围内稳定。这两种矿物都在斜角闪洞(一种富铁的绿泥石群矿物)和破碎的黄铜矿组合中观察到，表明物理或化学蚀变，可能两者都有。Palladogermanide还被发现与近端元组成的磁铁矿有关，可能表明fO2的相对增加。考虑到分馏、浓缩和形成具有ge优势化学物质的矿物所需的要求，这两种矿物都被认为是在500-600°C的温度下，在低fS2和fO2的条件下形成的。
{"title":"Marathonite, Pd25Ge9, and palladogermanide, Pd2Ge, two new platinum-group minerals from the Marathon deposit, Coldwell Complex, Ontario, Canada: Descriptions, crystal-chemical considerations, and genetic implications","authors":"A. McDonald, D. Ames, I. Kjarsgaard, L. Cabri, William Zhe, K. C. Ross, D. Good","doi":"10.3749/canmin.2100022","DOIUrl":"https://doi.org/10.3749/canmin.2100022","url":null,"abstract":"\u0000 Marathonite, Pd25Ge9, and palladogermanide, Pd2Ge, are two new platinum-group minerals discovered in the Marathon deposit, Coldwell Complex, Ontario, Canada. Marathonite is trigonal, space group P3, with a 7.391(1), c 10.477(2) Å, V 495.6(1) Å3, Z = 1. The six strongest lines of the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.436(10)(014,104,120,210), 2.374(29)(023,203,121,211), 2.148(100)(114,030), 1.759(10)(025,205,131,311), 1.3605(13)(233,323,036,306), and 1.2395(14)(144,414,330). Associated minerals include: vysotskite, Au-Ag alloy, isoferroplatinum, Ge-bearing keithconnite, majakite, coldwellite, ferhodsite-series minerals (cuprorhodsite-ferhodsite), kotulskite and mertieite-II, the base-metal sulfides, chalcopyrite, bornite, millerite and Rh-bearing pentlandite, oberthürite and torryweiserite, and silicates including a clinoamphibole and a Fe-rich chlorite-group mineral. Rounded, elongated grains of marathonite are up to 33 × 48 μm. Marathonite is white, but pinkish brown compared to palladogermanide and bornite. No streak or microhardness could be measured. The mineral shows no discernible pleochroism, bireflectance, or anisotropy. The reflectance values (%) in air for the standard COM wavelengths are: 40.8 (470 nm), 44.1 (546 nm), 45.3 (589 nm), and 47.4 (650 nm). The calculated density is 10.933 g/cm3, determined using the empirical formula and the unit-cell parameters from the refined crystal structure. The average result (n = 19) using energy-dispersive spectrometry is: Si 0.11, S 0.39, Cu 2.32, Ge 18.46, Pd 77.83, Pt 1.10, total 100.22 wt.%, corresponding to the empirical formula (based on 34 apfu): (Pd23.82Cu1.19Pt0.18)Σ25.19(Ge8.28S0.40Si0.13)∑8.81 and the simplified formula is Pd25Ge9. The name is for the town of Marathon, Ontario, Canada, after which the Marathon deposit (Coldwell complex) is named.\u0000 Results from electron backscattered diffraction show that palladogermanide is isostructural with synthetic Pd2Ge. Based on this, palladogermanide is considered to be hexagonal, space group , with a 6.712(1), c 3.408(1) Å, V 133.0(1), Z = 3. The seven strongest lines of the X-ray powder-diffraction pattern calculated for the synthetic analogue [d in Å (I)(hkl)] are: 2.392(100)(111), 2.211(58)(201), 2.197(43)(210), 1.937(34)(300), 1.846(16)(211), 1.7037(16)(002), and 1.2418(18)(321). Associated minerals are the same as for marathonite. Palladogermanide occurs as an angular, anhedral grain measuring 29 × 35 μm. It is white, but grayish-white when compared to marathonite, bornite, and chalcopyrite. Compared to zvyagintsevite, palladogermanide is a dull gray. No streak or microhardness could be measured. The mineral shows no discernible pleochroism, bireflectance, or anisotropy. The reflectance values (%) in air for the standard COM wavelengths for Ro and Ro' are: 46.8, 53.4 (470 nm), 49.5, 55.4 (546 nm), 50.1, 55.7 (589 nm), and 51.2, 56.5 (650 nm). The calculated density is 10.74 g/cm3, determined using the empirical form","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"45 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122797896","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Prevec, Savvas Anthony Largatzis, W. Brownscombe, T. Salge
The wide-reef facies of the Merensky Reef in the eastern part of the western lobe of the Bushveld Complex was sampled in order to better resolve otherwise spatially constrained variation in highly siderophile elements across this geological unit. The platinum group element mineralogy and whole-rock highly siderophile element concentrations were measured across two vertical sections in close proximity. In one section, the Merensky Reef unit was bound by top and bottom platinum group elements-enriched horizons (reefs) with a well-developed pegmatoidal phase in the top third of the intrareef pyroxenite, but with neither a top nor a bottom chromitite present. The other drill core section featured a thin (<1 cm thick) chromitite layer associated with the highest platinum group element concentrations of any rock in this study as the bottom reef, but with a chromitite-absent top reef, and very poor development of the pegmatoid. Primitive mantle-normalized profiles of the main lithological units show relatively flat, primitive mantle-like highly siderophile element abundances (Cr, V, Co, Ni, platinum group elements, Au and Cu) in the Merensky pyroxenite, with modest depletion in Ir-affiliated platinum group elements. The platinum group element-rich top and bottom reefs, and the pegmatoidal upper pyroxenites, display characteristic enrichment in the Pt-affiliated platinum group elements and undepleted Ir-affiliated platinum group elements. The leuconoritic hanging wall and footwall rocks show comparable highly siderophile element profiles, distinguished from one another by relative depletion in the Pt-affiliated platinum group elements of the footwall samples. The vertical variation in highly siderophile element abundances through both sections is characterized by low platinum group element abundances through the lower reef pyroxenite, with platinum group element, Au, and Cu ± Ni concentrations increasing through the upper pegmatoidal pyroxenite, and main enrichment peaks at the top and bottom reefs. Significant localized (centimeter-scale) zones of chalcophile metal depletion are present immediately above the top reef and below the bottom reef. In addition, a wider zone of Pt-affiliated platinum group elements (with Pd more depleted than Pt)-depletion was identified within the pegmatoidal pyroxenite around one meter below the top reef. The platinum group element mineralogy of the bottom reef consists mainly of platinum group element sulfides, with minor arsenides and antimonides. In contrast, the platinum group element mineralogy of the top reef, and the small amount of data from the intrareef pyroxenite, mainly consist of Pt-affiliated platinum group elements-Bi-tellurides. The Pt-sulfides are mainly equant, relatively coarse crystals (many grains between 50 to 100 μm2 area), contrasting with the Pt-affiliated platinum group elements-Sb-As and -Bi-Te minerals that tend be high aspect-ratio grains, occurring in veinlets or as rims on earlier-forming p
对Bushveld杂岩西叶东部的Merensky礁的宽礁相进行了采样，以便更好地解决该地质单元中高亲铁元素的空间限制变化。铂族元素矿物学和全岩高亲铁元素浓度在两个接近的垂直剖面上进行了测量。在一个剖面上，梅伦斯基礁单元被顶部和底部富铂族元素的层位(礁)所约束，在礁内辉石岩的顶部三分之一处有发育良好的伟晶岩相，但顶部和底部都没有铬铁矿。另一钻孔岩心剖面的底礁为薄(<1 cm厚)的铬铁矿层，其铂族元素浓度是本研究中所有岩石中最高的，但顶礁没有铬铁矿，类伟晶岩发育非常差。主要岩性单元的原始地幔归一化剖面显示，梅伦斯基辉石岩中亲铁元素(Cr、V、Co、Ni、铂族元素、Au和Cu)丰度相对平坦，呈原始地幔状，与ir相关的铂族元素有一定的亏缺。富铂族元素的顶、底礁和伟晶状上辉石岩均具有铂族元素富集和未亏缺铂族元素富集的特征。上盘和下盘白斑岩均表现出相当高的亲铁元素特征，其区别在于下盘样品中铂族元素的相对贫化。高亲铁元素丰度的垂直变化特征为:铂族元素丰度在礁体下部辉石岩中呈低丰度，铂族元素、Au和Cu±Ni浓度在礁体上部辉石岩中呈上升趋势，富集峰主要在礁体顶部和底部。显著的局部(厘米尺度)亲铜金属耗损区出现在顶部礁的正上方和底部礁的下方。此外，在顶部礁体下方约一米的伟晶状辉石岩中发现了一个更广泛的铂族元素(Pd比Pt更贫)耗损区。底礁铂族元素矿物学以铂族元素硫化物为主，含少量砷化物和锑化物。顶部礁体的铂族元素矿物学特征，以及礁内辉石岩的少量资料，主要由铂族元素-铋碲化物组成。与铂族元素sb - as和-Bi-Te等矿物相比，铂族元素硫化物主要为均匀、较粗的晶体(许多颗粒面积在50 ~ 100 μm2之间)，而铂族元素的铂族元素sb - as和bi - te矿物则倾向于高纵横比的颗粒，在早期形成的铂族元素相中呈细脉状或呈边缘状。这些Te-As-Bi-Sb化合物与绿泥石、放线石、石英和黄铜矿密切相关，与低温下的二次沉积和与水相结合一致。提出了Merensky单元作为岩浆脉冲侵入至少半结晶的寄主岩石的模型，随后是含水流体饱和和局部迁移，并结合岩浆脉冲顶部和底部接触处晚期岩浆流体的浓度。铂系铂族元素从顶部礁上方(厘米尺度)、从下垫1 - 2米的辉石岩以及从底部礁下垫数厘米的铂族元素晚期再活化，为礁体添加了额外的铂族元素，即晚期铂族元素- te - as - bi - sb矿物，而与最初礁体中是否存在铬铁矿无关。
{"title":"PGE distribution in Merensky wide-reef facies of the Bushveld Complex, South Africa: Evidence for localized hydromagmatic control","authors":"S. Prevec, Savvas Anthony Largatzis, W. Brownscombe, T. Salge","doi":"10.3749/canmin.2100033","DOIUrl":"https://doi.org/10.3749/canmin.2100033","url":null,"abstract":"\u0000 The wide-reef facies of the Merensky Reef in the eastern part of the western lobe of the Bushveld Complex was sampled in order to better resolve otherwise spatially constrained variation in highly siderophile elements across this geological unit. The platinum group element mineralogy and whole-rock highly siderophile element concentrations were measured across two vertical sections in close proximity. In one section, the Merensky Reef unit was bound by top and bottom platinum group elements-enriched horizons (reefs) with a well-developed pegmatoidal phase in the top third of the intrareef pyroxenite, but with neither a top nor a bottom chromitite present. The other drill core section featured a thin (<1 cm thick) chromitite layer associated with the highest platinum group element concentrations of any rock in this study as the bottom reef, but with a chromitite-absent top reef, and very poor development of the pegmatoid.\u0000 Primitive mantle-normalized profiles of the main lithological units show relatively flat, primitive mantle-like highly siderophile element abundances (Cr, V, Co, Ni, platinum group elements, Au and Cu) in the Merensky pyroxenite, with modest depletion in Ir-affiliated platinum group elements. The platinum group element-rich top and bottom reefs, and the pegmatoidal upper pyroxenites, display characteristic enrichment in the Pt-affiliated platinum group elements and undepleted Ir-affiliated platinum group elements. The leuconoritic hanging wall and footwall rocks show comparable highly siderophile element profiles, distinguished from one another by relative depletion in the Pt-affiliated platinum group elements of the footwall samples. The vertical variation in highly siderophile element abundances through both sections is characterized by low platinum group element abundances through the lower reef pyroxenite, with platinum group element, Au, and Cu ± Ni concentrations increasing through the upper pegmatoidal pyroxenite, and main enrichment peaks at the top and bottom reefs. Significant localized (centimeter-scale) zones of chalcophile metal depletion are present immediately above the top reef and below the bottom reef. In addition, a wider zone of Pt-affiliated platinum group elements (with Pd more depleted than Pt)-depletion was identified within the pegmatoidal pyroxenite around one meter below the top reef. The platinum group element mineralogy of the bottom reef consists mainly of platinum group element sulfides, with minor arsenides and antimonides. In contrast, the platinum group element mineralogy of the top reef, and the small amount of data from the intrareef pyroxenite, mainly consist of Pt-affiliated platinum group elements-Bi-tellurides. The Pt-sulfides are mainly equant, relatively coarse crystals (many grains between 50 to 100 μm2 area), contrasting with the Pt-affiliated platinum group elements-Sb-As and -Bi-Te minerals that tend be high aspect-ratio grains, occurring in veinlets or as rims on earlier-forming p","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"16 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127752505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
We have characterized the distribution of noble metals among six styles of magmatic sulfide mineralization in the Montagnais Sill Complex of the Labrador Trough in northern Québec using optical and electron microscopy combined with laser ablation-inductively coupled plasma-mass spectrometry trace element analysis of sulfides. The principal sulfide minerals include pyrrhotite, chalcopyrite, and pentlandite with accessory sphalerite and sulfarsenides. In addition, cubanite, troilite, and mackinawite are present in ultramafic-hosted assemblages. The precious metal mineral assemblages are dominated by tellurides, Ag-rich gold, and sperrylite which generally occur at the margins of sulfides. Few iridium-group platinum group element- and Rh-bearing grains were identified and mass-balance calculations show that these elements are generally hosted in pyrrhotite and pentlandite. Virtually all Pt and Au are hosted in precious metal grains, whereas Pd is distributed between precious metal grains and pentlandite. Where present, sulfarsenides are a key host of iridium-group platinum group element, Rh, Pd, Te, and Au. The presence of troilite, cubanite, and mackinawite and the absence of pentlandite exsolution lamellae in the ultramafic-hosted sulfides indicates an initial sulfide melt with a high metal/S ratio. Sulfarsenides present among globular sulfide assemblages derive from an immiscible As-rich melt that exsolved from the sulfide melt in response to the assimilation of the As-bearing floor rocks. In this study, the composition of sulfides is consistent with those derived from Ni-Cu-dominated deposits and not platinum group element-dominated deposits.
{"title":"Distribution of noble metals in magmatic sulfide occurrences in the Montagnais Sill Complex, Labrador Trough, Canada","authors":"William D. Smith, W. Maier, I. Bliss","doi":"10.3749/canmin.2000119","DOIUrl":"https://doi.org/10.3749/canmin.2000119","url":null,"abstract":"\u0000 We have characterized the distribution of noble metals among six styles of magmatic sulfide mineralization in the Montagnais Sill Complex of the Labrador Trough in northern Québec using optical and electron microscopy combined with laser ablation-inductively coupled plasma-mass spectrometry trace element analysis of sulfides. The principal sulfide minerals include pyrrhotite, chalcopyrite, and pentlandite with accessory sphalerite and sulfarsenides. In addition, cubanite, troilite, and mackinawite are present in ultramafic-hosted assemblages. The precious metal mineral assemblages are dominated by tellurides, Ag-rich gold, and sperrylite which generally occur at the margins of sulfides. Few iridium-group platinum group element- and Rh-bearing grains were identified and mass-balance calculations show that these elements are generally hosted in pyrrhotite and pentlandite. Virtually all Pt and Au are hosted in precious metal grains, whereas Pd is distributed between precious metal grains and pentlandite. Where present, sulfarsenides are a key host of iridium-group platinum group element, Rh, Pd, Te, and Au. The presence of troilite, cubanite, and mackinawite and the absence of pentlandite exsolution lamellae in the ultramafic-hosted sulfides indicates an initial sulfide melt with a high metal/S ratio. Sulfarsenides present among globular sulfide assemblages derive from an immiscible As-rich melt that exsolved from the sulfide melt in response to the assimilation of the As-bearing floor rocks. In this study, the composition of sulfides is consistent with those derived from Ni-Cu-dominated deposits and not platinum group element-dominated deposits.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"55 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129392334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Near-surface supergene ores of the Merensky Reef in the Bushveld Complex, South Africa, contain economic grades of platinum-group elements, however, these are currently uneconomic due to low recovery rates. This is the first study that investigates the variation in platinum-group elements in pristine and supergene samples of the Merensky Reef from five drill cores from the eastern Bushveld. The samples from the Richmond and Twickenham farms show different degrees of weathering. The whole-rock platinum-group element distribution was studied by inductively coupled plasma-mass spectrometry and the platinum-group minerals were investigated by reflected-light microscopy, scanning electron microscopy, and electron microprobe analysis. In pristine (“fresh”) Merensky Reef samples, platinum-group elements occur mainly as discrete platinum-group minerals, such as platinum-group element-sulfides (cooperite–braggite) and laurite as well as subordinate platinum-group element-bismuthotellurides and platinum-group element-arsenides, and also in solid solution in sulfides (especially Pd in pentlandite). During weathering, Pd and S were removed, resulting in a platinum-group mineral mineralogy in the supergene Merensky Reef that mainly consists of relict platinum-group minerals, Pt-Fe alloys, and Pt-oxides/hydroxides. Additional proportions of platinum-group elements are hosted by Fe-hydroxides and secondary hydrosilicates (e.g., serpentine group minerals and chlorite). In supergene ores, only low recovery rates (ca. 40%) are achieved due to the polymodal and complex platinum-group element distribution. To achieve higher recovery rates for the platinum-group elements, hydrometallurgical or pyrometallurgical processing of the bulk ore would be required, which is not economically viable with existing technology.
{"title":"Supergene mobilization and redistribution of platinum-group elements in the Merensky Reef, eastern Bushveld Complex, South Africa","authors":"Maximilian Korges, M. Junge, G. Borg, T. Oberthür","doi":"10.3749/canmin.2100023","DOIUrl":"https://doi.org/10.3749/canmin.2100023","url":null,"abstract":"\u0000 Near-surface supergene ores of the Merensky Reef in the Bushveld Complex, South Africa, contain economic grades of platinum-group elements, however, these are currently uneconomic due to low recovery rates. This is the first study that investigates the variation in platinum-group elements in pristine and supergene samples of the Merensky Reef from five drill cores from the eastern Bushveld. The samples from the Richmond and Twickenham farms show different degrees of weathering. The whole-rock platinum-group element distribution was studied by inductively coupled plasma-mass spectrometry and the platinum-group minerals were investigated by reflected-light microscopy, scanning electron microscopy, and electron microprobe analysis.\u0000 In pristine (“fresh”) Merensky Reef samples, platinum-group elements occur mainly as discrete platinum-group minerals, such as platinum-group element-sulfides (cooperite–braggite) and laurite as well as subordinate platinum-group element-bismuthotellurides and platinum-group element-arsenides, and also in solid solution in sulfides (especially Pd in pentlandite). During weathering, Pd and S were removed, resulting in a platinum-group mineral mineralogy in the supergene Merensky Reef that mainly consists of relict platinum-group minerals, Pt-Fe alloys, and Pt-oxides/hydroxides. Additional proportions of platinum-group elements are hosted by Fe-hydroxides and secondary hydrosilicates (e.g., serpentine group minerals and chlorite).\u0000 In supergene ores, only low recovery rates (ca. 40%) are achieved due to the polymodal and complex platinum-group element distribution. To achieve higher recovery rates for the platinum-group elements, hydrometallurgical or pyrometallurgical processing of the bulk ore would be required, which is not economically viable with existing technology.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"40 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131815973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nearly monomineralic stratiform chromitite seams of variable thickness (millimeters to meters) occur in many of the world's layered mafic-ultramafic intrusions. These seams are often associated with economically significant quantities of platinum group metals, yet the petrogenesis of these societally important materials remains enigmatic. Here we evaluate processes associated with late-magmatic (postcumulus) textural maturation of chromitite seams from four layered mafic-ultramafic intrusions of different ages and sizes. From largest to smallest, these intrusions are the ∼2060 Ma Bushveld Complex (South Africa), the ∼2710 Ma Stillwater Complex (USA), the ∼1270 Ma Muskox Intrusion (Canada), and the ∼60 Ma Rum Eastern Layered Intrusion (Scotland). Three endmember chromitite textures are described, based on chromite grain size and degree of textural equilibration: (1) coarse-grained chromite crystals (>0.40 mm) that occur in the central portions of seams and exhibit high degrees of solid-state textural equilibration; (2) fine-grained chromite crystals (0.11–0.44 mm) at the margins of seams in contact with and disseminated throughout host anorthosite or pyroxenite; and (3) fine-grained chromite crystals (0.005–0.28 mm) hosted within intra-seam orthopyroxene, clinopyroxene, and olivine oikocrysts. Crystal size distribution and spatial distribution pattern analyses are consistent with coarsening occurring through processes of textural maturation, including the sintering of grains by coalescence. We propose that textural maturation initially occurred in the supra-solidus state followed by an important stage of solid-state textural maturation and that these equilibration processes played a major role in the eventual microstructural and compositional homogeneity of the chromitite seams.
在世界上许多层状基性-超基性侵入岩中都有厚度不等(毫米到米)的几乎单矿物层状铬铁矿。这些矿层通常与经济上重要的铂族金属有关，但这些具有重要社会意义的材料的岩石成因仍然是一个谜。在这里，我们评估了来自4个不同年龄和大小的层状基性-超基性侵入体的铬铁矿的岩浆晚期(积云后)结构成熟过程。从大到小依次为~ 2060 Ma Bushveld杂岩(南非)、~ 2710 Ma Stillwater杂岩(美国)、~ 1270 Ma Muskox杂岩(加拿大)和~ 60 Ma Rum东部分层杂岩(苏格兰)。根据铬铁矿的晶粒尺寸和结构平衡程度，描述了三种端部铬铁矿结构:(1)粗粒铬铁矿晶体(>0.40 mm)，出现在接缝的中心部分，表现出高度的固态结构平衡;(2)细粒铬铁矿晶体(0.11 ~ 0.44 mm)，在煤层边缘与主斜长岩或辉石岩接触并浸染;(3)细粒铬铁矿晶体(0.005-0.28 mm)赋存于缝内的正辉石、斜辉石和橄榄石泡晶中。晶粒尺寸分布和空间分布模式分析表明，晶粒的粗化是通过织构成熟过程发生的，包括晶粒的聚结烧结。我们认为，结构成熟最初发生在超固态，随后是固态结构成熟的重要阶段，这些平衡过程在铬铁矿最终的微观结构和成分均匀性中发挥了重要作用。
{"title":"Sintering as a key process in the textural evolution of chromitite seams in layered mafic-ultramafic intrusions","authors":"Emma J. Hunt, B. O’Driscoll, J. Day","doi":"10.3749/canmin.2100021","DOIUrl":"https://doi.org/10.3749/canmin.2100021","url":null,"abstract":"\u0000 Nearly monomineralic stratiform chromitite seams of variable thickness (millimeters to meters) occur in many of the world's layered mafic-ultramafic intrusions. These seams are often associated with economically significant quantities of platinum group metals, yet the petrogenesis of these societally important materials remains enigmatic. Here we evaluate processes associated with late-magmatic (postcumulus) textural maturation of chromitite seams from four layered mafic-ultramafic intrusions of different ages and sizes. From largest to smallest, these intrusions are the ∼2060 Ma Bushveld Complex (South Africa), the ∼2710 Ma Stillwater Complex (USA), the ∼1270 Ma Muskox Intrusion (Canada), and the ∼60 Ma Rum Eastern Layered Intrusion (Scotland). Three endmember chromitite textures are described, based on chromite grain size and degree of textural equilibration: (1) coarse-grained chromite crystals (>0.40 mm) that occur in the central portions of seams and exhibit high degrees of solid-state textural equilibration; (2) fine-grained chromite crystals (0.11–0.44 mm) at the margins of seams in contact with and disseminated throughout host anorthosite or pyroxenite; and (3) fine-grained chromite crystals (0.005–0.28 mm) hosted within intra-seam orthopyroxene, clinopyroxene, and olivine oikocrysts. Crystal size distribution and spatial distribution pattern analyses are consistent with coarsening occurring through processes of textural maturation, including the sintering of grains by coalescence. We propose that textural maturation initially occurred in the supra-solidus state followed by an important stage of solid-state textural maturation and that these equilibration processes played a major role in the eventual microstructural and compositional homogeneity of the chromitite seams.","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125548744","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Most of the World's platinum-group element ore deposits occur as thin stratiform layers within layered intrusions. These layers generally contain disseminated base-metal sulfides or chromite. However, cryptic platinum-group element deposits also occur without chromite or base-metal sulfides in what are known as low-S-high platinum-group element deposits. The origin of these deposits is not clearly understood. The Luanga Complex hosts the largest platinum-group elements resource in South America (i.e., 142 Mt at 1.24 ppm Pt + Pd + Au and 0.11% Ni) and hosts both a platinum-group element deposit containing disseminated base-metal sulfides (style 1) and a low-S-high platinum-group element deposit (style 2). It therefore offers the opportunity to compare the two deposit types in the same overall geological setting and consider how the low-S-high platinum-group element deposit could have formed. The first deposit style is termed the Sulfide zone and consists of a 10–50 meter-thick interval with disseminated base metal sulfides, whereas the second style is named low-S-high-Pt-Pd zone and consists of 2–10 meter-thick discontinuous lenses of 1–5 meter-thick sulfide- and oxide-free harzburgite and orthopyroxenite with discrete platinum-group minerals. Secondary assemblages commonly replace primary igneous minerals to a variable extent throughout the deposit, and thus allow for investigating the effects of post-cumulus alteration on the distribution of a wide range of chalcophile elements in a magmatic sulfide deposit at both whole-rock and mineral scale. This study presents the whole-rock distribution of S, platinum-group elements, and Te, As, Bi, Sb, and Se in both mineralization styles and the concentration of trace elements in base-metal sulfides from the Sulfide zone. The Sulfide zone has Pt/Pd ratios around 0.5 and high concentrations of Te, As, Bi, Sb, and Se, whereas the low-S-high-platinum-group element zone has Pt/Pd ratios greater than 1 and much lower Se, Te, and Bi concentrations, but comparable As and Sb contents. This is reflected in the platinum-group element assemblage, comprising bismuthotellurides in the Sulfide zone and mostly arsenides and antimonides in the low-S, high platinum-group elements zone. Moreover, the base-metal sulfides from the Sulfide zone have anomalously high As contents (50–500 ppm), which suggest that the sulfide liquid segregated from a very As-rich silicate magma, possibly illustrated by an average komatiitic basalt that assimilated a mixture of upper continental crust and black shales. We interpret the low-S-high platinum-group elements zone as a product of S loss from magmatic sulfides during post-cumulus alteration of the Luanga Complex. Selenium, Te, Bi, and Pd were also lost together with S, whereas As and Sb were expelled from base-metal sulfide structures and combined with platinum-group elements to form platinum-group minerals, suggesting they may play a role fixating platinum-group elements during altera
{"title":"The effects of post-cumulus alteration on the distribution of chalcophile elements in magmatic sulfide deposits and implications for the formation of low-S-high-PGE zones: The Luanga deposit, Carajás Mineral Province, Brazil","authors":"E. Mansur, S. Barnes, C. F. Ferreira Filho","doi":"10.3749/canmin.2100018","DOIUrl":"https://doi.org/10.3749/canmin.2100018","url":null,"abstract":"\u0000 Most of the World's platinum-group element ore deposits occur as thin stratiform layers within layered intrusions. These layers generally contain disseminated base-metal sulfides or chromite. However, cryptic platinum-group element deposits also occur without chromite or base-metal sulfides in what are known as low-S-high platinum-group element deposits. The origin of these deposits is not clearly understood. The Luanga Complex hosts the largest platinum-group elements resource in South America (i.e., 142 Mt at 1.24 ppm Pt + Pd + Au and 0.11% Ni) and hosts both a platinum-group element deposit containing disseminated base-metal sulfides (style 1) and a low-S-high platinum-group element deposit (style 2). It therefore offers the opportunity to compare the two deposit types in the same overall geological setting and consider how the low-S-high platinum-group element deposit could have formed. The first deposit style is termed the Sulfide zone and consists of a 10–50 meter-thick interval with disseminated base metal sulfides, whereas the second style is named low-S-high-Pt-Pd zone and consists of 2–10 meter-thick discontinuous lenses of 1–5 meter-thick sulfide- and oxide-free harzburgite and orthopyroxenite with discrete platinum-group minerals. Secondary assemblages commonly replace primary igneous minerals to a variable extent throughout the deposit, and thus allow for investigating the effects of post-cumulus alteration on the distribution of a wide range of chalcophile elements in a magmatic sulfide deposit at both whole-rock and mineral scale. This study presents the whole-rock distribution of S, platinum-group elements, and Te, As, Bi, Sb, and Se in both mineralization styles and the concentration of trace elements in base-metal sulfides from the Sulfide zone. The Sulfide zone has Pt/Pd ratios around 0.5 and high concentrations of Te, As, Bi, Sb, and Se, whereas the low-S-high-platinum-group element zone has Pt/Pd ratios greater than 1 and much lower Se, Te, and Bi concentrations, but comparable As and Sb contents. This is reflected in the platinum-group element assemblage, comprising bismuthotellurides in the Sulfide zone and mostly arsenides and antimonides in the low-S, high platinum-group elements zone. Moreover, the base-metal sulfides from the Sulfide zone have anomalously high As contents (50–500 ppm), which suggest that the sulfide liquid segregated from a very As-rich silicate magma, possibly illustrated by an average komatiitic basalt that assimilated a mixture of upper continental crust and black shales. We interpret the low-S-high platinum-group elements zone as a product of S loss from magmatic sulfides during post-cumulus alteration of the Luanga Complex. Selenium, Te, Bi, and Pd were also lost together with S, whereas As and Sb were expelled from base-metal sulfide structures and combined with platinum-group elements to form platinum-group minerals, suggesting they may play a role fixating platinum-group elements during altera","PeriodicalId":134244,"journal":{"name":"The Canadian Mineralogist","volume":"12 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124460011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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