کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
8910131 1637481 2018 37 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Strongly negative δ34S values associated with secondary pyrite above and below the J-M Reef, Stillwater Complex, Montana
موضوعات مرتبط
مهندسی و علوم پایه علوم زمین و سیارات ژئوشیمی و پترولوژی
پیش نمایش صفحه اول مقاله
Strongly negative δ34S values associated with secondary pyrite above and below the J-M Reef, Stillwater Complex, Montana
چکیده انگلیسی
Previous sulfur isotope studies of the Stillwater Complex, and in particular the J-M Reef, have noted the generally restricted range of δ34S values in the range of 0 ± 2.5‰ (e.g., Zientek and Ripley, 1990; Ripley et al., 2017). Detailed studies of high-S zones in both the hanging wall of the Reef Package, which contains the J-M Reef, and the footwall within the Reef Package but below the mineralized J-M-Reef, indicate the presence of significant quantities of secondary pyrite. The pyrite-rich intervals are characterized by δ34S values that strongly differ from those of the J-M Reef, in the range of 0.2 to −17.4‰. The pyrite-rich rocks above and below the J-M Reef are both serpentinized lherzolites. Although the J-M Reef is locally strongly altered to clinozoisite-epidote-rich assemblages, only the sepentinized lherzolites show anomalously low δ34S values. The highly negative δ34S values of the pyrite-rich assemblages result from oxidation processes and S isotope fractionation between reduced and oxidized S species. One possible process involves the production of a mixed sulfate-sulfide fluid with pyrite produced from H2S with low δ34S values. A second alternative is that infiltration of an oxidized fluid and interaction with sulfide-bearing rocks of the Complex produced a sulfate-rich fluid that then underwent partial reduction to sulfide via reaction with reduced Fe-bearing minerals. Strongly negative δ34S values would characterize secondary pyrite produced as a result of either process due to the large S isotope fractionation between oxidized and reduced S species at hydrothermal temperatures of ~400 °C or below. The varying degrees of alteration and restricted pyrite-rich intervals with highly negative S isotope signatures suggest that fluid infiltration was not pervasive; secondary pyrite that was produced as a result of redox-driven reactions is preserved only in olivine-rich lithologies characterized by a high degree of serpentinization.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Geology - Volume 493, 20 August 2018, Pages 58-66
نویسندگان
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