Sulfur and oxygen isotopic systematics of the 1982 eruptions of El Chichón Volcano, Chiapas, Mexico
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Anhydrite
δ34S
Mineral redox buffer
Mechanisms for the enrichment and re-precipitation of gold in the giant Jiaodong gold deposits (eastern North China Craton) remain poorly constrained. To better understand the mineralization mechanism, we did in situ analyses of S isotopes on sulfides such as pyrite, pyrrhotite, galena and chalcopyrite from the disseminated (altered-rock type) and quartz-vein type gold deposits by femtosecond laser ablation coupled multi-collector inductively coupled plasma mass spectrometry. Pyrites from the altered-rock type gold deposit show δ34S values in the range from 7.4 to 11.3 ‰, which is obviously heavier than the quartz-vein type gold deposits with δ34S = 6.2 ∼ 8.8 ‰. Traditionally, the difference of sulfur isotopic compositions between the two types of gold deposits was attributed to the change in oxygen fugacity. However, we found that, from early to late metallogenic stage, sulfur isotopes of pyrites from the altered rock type gold deposits tend to decrease gradually and pyrrhotites can always be observed in the third stage. Moreover, the S isotopic compositions (δ34S = 7.9 to 8.2 ‰) of the pyrites coexisting with magnetite are comparable with those (δ34S = 6.2 to 8.0 ‰) of the pyrites coexisting with pyrrhotite in the quartz vein type gold deposits. These features indicate that the decrease of sulfur isotopes in pyrites was not caused by increase of oxygen fugacity. We suggest that the S isotopic and fO2 variation could be ascribed to an increase of pH of the ore-forming fluid, which is supported by the typically quartz dissolution and common occurrence of calcite and pyrrhotite in the late metallogenic stage (the third stage) and an overall decrease of aluminum contents of quartz from core to rim. We further proposed that the variation of pH of ore-forming fluids is probably related to a process of decompression due to development and enlargement of fractures filled with ore-forming fluids. Gold enrichment in the main ore-forming stage of the northwest Jiaodong gold deposit probably was realized by multiple phases of fluid pressure fluctuation, which subsequently led to repeatedly dissolution and re-precipitation of Au from pyrites due to decreasing oxygen fugacity and increasing pH values of the ore-forming fluids.
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ABSTRACT In this study, we present a detailed investigation of C-O-S-Sr isotope systematics and elemental analysis of secondary sulfates and associated host-rock carbonates of Cambrian to Devonian sedimentary successions along the eastern flank of the Michigan Basin, Ontario. This study evaluates the diagenetic evolution of pore fluids and their sources in fracture-fill and replacement sulfate minerals in low-permeability carbonate units in the Michigan Basin. Secondary sulfates, represented by gypsum and anhydrite, contain various petrographic types, represented by vug- and fracture-filling fibrous anhydrite in the Cambrian (δ18O vary between 16.8 to 17.6‰ VPDB and δ34S 28.3 to 29.0‰ CDT, 87Sr/86Sr ratios vary from 0.70834 to 0.70991, respectively) and Ordovician fibrous anhydrite (δ18O 16.8‰, δ34S 28.2‰, 87Sr/86Sr ratios 0.70829). These phases display mainly uniform REE patterns with Y/Ho and Zr/Hf ratios, flat La*, Gd*, and Y*, and enriched LREEs. In the Silurian strata, idiotopic satin-spar δ18O values vary between 4.0 and 8.3‰, δ34S 23.4 and 31.4‰ with 87Sr/86Sr ratios 0.70816–0.70866, xenotopic porphyroblast gypsum δ18O values vary between 4.5 and 13.3‰, δ34S 22.6 to 33.1‰, with 87Sr/86Sr ratios of 0.70850–0.70880, alabastrine gypsum δ18O values vary between 4.2 and 11.7‰, δ34S 23.1 to 26.9‰, with 87Sr/86Sr ratios of 0.70816–0.70876 and felted anhydrite δ18O values of 11.1‰, δ34S 27.4‰, with a 87Sr/86Sr ratio of 0.70849. These geochemical proxies suggest a comparable sulfate-rich source for both age groups under similar geochemical conditions. Gypsum in the Silurian Salina Group displays a wide range of REE values with Y/Ho, and Zr/Hf ratios, Nd/YbN and Pr/YbN, flat to strong Ce/Ce*, and a flat to strong Eu/Eu* anomaly, Gd/LaN, Tb/LaN, and Sm/LaN. These sulfates formed at burial from fluids of variable isotope compositions, chemical compositions, and temperatures. The sources of these fluids range from brines migrating from a deeper part of the basin forming anhydrite in the Cambrian and Ordovician sequences which were also affected by dolomitization and later hydrothermal fluid influx, to rehydration of gypsum at shallower burial depths and affected by salt dissolution and incursion of meteoric water during and following the Alleghenian orogeny.
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Anhydrite
δ34S
Sichuan basin
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Six anhydrite samples from the submarine hydrothermal sulphide/sulphate mineral deposits found along the crest of the East Pacific Rise at 21 °N have been examined for filling temperature of fluid inclusions and for 34S/32S and 18O/16O ratios. The anhydrite was precipitated upon mixing of hot (260–350°C), SO42--poor hydrothermal fluids with cold seawater at various proportions, which is reflected in a large variation in the filling temperatures ranging from 180°C to almost the highest exit temperatures. Seawater sulphate origin for anhydrite-sulphur is indicated by the δ34S values that are essentially identical with the present-day seawater sulphate value, whereas the δ18O values are up to 2‰ higher than the seawater sulphate value. The anhydrites are not in oxygen isotopic equilibrium with the mixed solution at measured exit temperatures of 260 to 350°C. However, this enrichment of 18O may be attributed to partial equilibration of fine-grained anhydrite with solutions at lower temperatures after deposition. Absence of anhydrite at dead vents suggests that SO42- slightly enriched in 18O is added to seawater sulphate owing to dissolution of anhydrite after the cessation of a high temperature stage of the hydrothermal activity.
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