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Item type:Publication, Distribution of indium, germanium, gallium and other minor and trace elements in polymetallic ores from a porphyry system: the Morococha district, Peru(Elsevier, 2021-09-01)We report indium, germanium, gallium, and other minor and trace elements contents in sphalerite, chalcopyrite, galena, and tetrahedrite-tennantite occurring in skarn and skarn-free (“Cordilleran”) polymetallic mantos and vein ore bodies in the Miocene porphyry-related Morococha District, Central Peru. Among the investigated minerals, LA-ICP-MS measurements indicate that In and Ga concentrate mostly in sphalerite (Inter-Quartile Range [IQR] 217–2.7 ppm and up to 4608 ppm In; IQR 61–2.0 ppm and up to 2137 ppm Ga) and chalcopyrite (IQR 109–32 ppm and up to 1070 ppm In; IQR 62–1.5 ppm and up to 630 ppm Ga). In coeval generations of sphalerite and chalcopyrite, the contents of In and Ga in sphalerite are at least two times higher than in chalcopyrite. Germanium content is generally low in the four analyzed minerals (IQR 1.2–0.19 ppm), although late Fe-poor sphalerite may yield much higher values (IQR 129–74 ppm). Certain trace element contents appear to correlate with (i) the evolving characteristics of the hydrothermal fluids during individual mineralization events, and (ii) the location of the studied ore bodies relative to the hydrothermal feeders. The highest In values in sphalerite are found in high-sulfidation assemblages in Cordilleran polymetallic veins and, with lower amounts, in low-sulfidation assemblages in skarn bodies. In intermediate-sulfidation assemblages in Cordilleran mineralization, In content decreases from early to late generations of sphalerite, while that of Ge increases. Spatial trace-element trends in Cordilleran veins and replacement bodies formed during the so-called “Morococha district-scale polymetallic event” include, from porphyry-distal to porphyry-proximal locations: i) In and Cu, and to a lesser extent Ga, enrichment in sphalerite; ii) Se and Hg enrichment and Sn and Ag depletion in chalcopyrite; iii) In enrichment in galena; and iv) Ag depletion in tetrahedrite-tennantite. Our dataset suggests that In is incorporated in the sphalerite crystal lattice via coupled substitutions involving Cu and subordinately also Sn and Ag. Availability of Cu in the mineralizing fluids is therefore key to In enrichment in sphalerite. Progressive dilution of metal-rich magmatic-hydrothermal fluids and Cu precipitation probably account for the progressive In depletion in distal-to-porphyry Zn-Pb-Ag and Ag-Pb Cordilleran polymetallic mineralization and in late sphalerite generations in intermediate-sulfidation assemblages. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Trace element composition and U-Pb ages of cassiterite from the Bolivian tin belt(Springer Science and Business Media Deutschland GmbH, 2021-11-01)The Bolivian tin belt is a metallogenic province in the Eastern Cordillera of the Andes known for its Sn, W, Ag, and base metal deposits. Cassiterite, which is a major constituent in many magmatic-hydrothermal ore deposits from the Bolivian tin belt, can incorporate dozens of elements within its crystal lattice, making it a useful geological tracer mineral and also a potential host of critical elements. New U-Pb dating of cassiterite yields Late Triassic (Kellhuani deposit) and Late Oligocene to earliest Miocene (Viloco, Huanuni, and Llallagua deposits) ages. These ages confirm that Sn mineralization in the Bolivian tin belt occurred at least in two separate events during two major magmatic episodes apparently triggered by mantle upwelling, decompression melting, and basalt production promoting high heat flow into the overlying crust. The composition of studied hydrothermal cassiterite yields some geochemical trends that are attributed to its distance to the causative intrusion and/or level of emplacement. For example, cassiterite is generally enriched in Nb and Ta and yields higher Ti/Zr and Ti/Sc ratios in samples from xenothermal ore deposits located adjacent to intrusive complexes relative to shallow xenothermal and epithermal ore deposits. Therefore, these geochemical trends in cassiterite are useful tracers pointing to magmatic-hydrothermal centers. REE distribution in cassiterite was likely influenced by boiling processes, which resulted in tetrad-type irregularities. Cassiterite from the Bolivian tin belt is unattractive as a source for Nb (interquartile range [IQR] 4.84–0.037 ppm), Ta (IQR 0.0924–0.0126 ppm), and Ge (IQR 3.92–0.776 ppm). Some deposits, however, contain cassiterite relatively enriched in In (IQR 96.9–9.78 ppm, up to 1414 ppm) and Ga (IQR 92.1–3.03, up to 7437 ppm), that could constitute an attractive supplementary source for these elements in addition to sulfide minerals in the same deposits. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Geology, mineralogy, and cassiterite geochronology of the Ayawilca Zn-Pb-Ag-In-Sn-Cu deposit, Pasco, Peru(Springer Science+Business Media, 2021-09-13)The Ayawilca deposit in Pasco, Peru, represents the most significant recent base-metal discovery in the central Andes and one of the largest undeveloped In resources globally. As of 2018, it hosts an 11.7 Mt indicated resource grading 6.9% Zn, 0.16% Pb, 15 g/t Ag, and 84 g/t In, an additional 45.0 Mt inferred resource grading 5.6% Zn, 0.23% Pb, 17 g/t Ag, and 67 g/t In, and a separate Sn-Cu-Ag inferred resource of 14.5 Mt grading 0.63% Sn, 0.21% Cu, and 18 g/t Ag. Newly obtained U–Pb dates for cassiterite by LA-ICP-MS (22.77 ± 0.41 and 23.05 ± 2.06 Ma) assign the Ayawilca deposit to the Miocene polymetallic belt of central Peru. The polymetallic mineralization occurs as up to 70-m-thick mantos hosted by carbonate rocks of the Late Triassic to Early Jurassic Pucará Group, and subordinately, as steeply dipping veins hosted by rocks of the Pucará Group and overlying Cretaceous sandstones-siltstones of the Goyllarisquizga Group. Relicts of a distal retrograde magnesian skarn and cassiterite (stage pre-A) were identified in the deepest mantos. The volumetrically most important mineralization at Ayawilca comprises a low-sulfidation assemblage (stage A) with quartz, pyrrhotite, arsenopyrite, chalcopyrite, Fe-rich sphalerite, and traces of stannite and herzenbergite. Stage A sphalerite records progressive Fe depletion, from 33 to 10 mol% FeS, which is compatible with the observed transition from low- to a subsequent intermediate-sulfidation stage (B) marked by the crystallization of abundant pyrite and marcasite. Finally, during a later intermediate-sulfidation stage (C) sphalerite (up to 11 mol% FeS), galena, native bismuth, Cu-Pb-Ag sulfosalts, siderite, Mn-Fe carbonates, kaolinite, dickite, and sericite were deposited. This paragenetic evolution shows striking similarities with that at the Cerro de Pasco Cordilleran-type polymetallic deposit, even if at Ayawilca stage C did not reach high-sulfidation conditions. The occurrence of an early retrograde skarn assemblage suggests that the manto bodies at Ayawilca formed at the transition between distal skarn and skarn-free (Cordilleran-type) carbonate-replacement mineralization. Mineral assemblages define a T-fS2 evolutionary path close to the pyrrhotite-pyrite boundary. Buffering of hydrothermal fluids by underlying Devonian carbonaceous phyllites of the Excelsior Group imposed highly reduced conditions during stage A mineralization (logfO2 < − 30 atm). The low fO2 favored efficient Sn mobility during stages pre-A and A, in contrast to other known ore deposits in the polymetallic belt of central Peru, in which the occurrence of Sn minerals is minor. Subsequent cooling, progressive sealing of vein walls, and decreasing buffering potential of the host rocks promoted the shift from low- (stage A) to intermediate-sulfidation (stages B and C) states. LA-ICP-MS analyses reveal significant In contents in Fe-rich sphalerite (up to 1.7 wt%), stannite (up to 1908 ppm), and chalcopyrite (up to 1185 ppm). The highest In content was found in stage A sphalerite that precipitated along with chalcopyrite and stannite, thus pointing to the early, low-sulfidation assemblage as prospective for this high-tech metal in similar mineral systems. Indium was likely incorporated into the sphalerite crystal lattice via Cu+ + In3+ ↔ 2 Zn2+ and (Sn, Ge)4+ + (Ga, In)3+ + (Cu + Ag)+ ↔ 4 Zn2+ coupled substitutions. Indium incorporation mechanisms into the stannite and chalcopyrite crystal lattices remain unclear.