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Pyrite records fluid evolution: sulfur sources controls on arsenic speciation and zonation
Journal article   Open access   Peer reviewed

Pyrite records fluid evolution: sulfur sources controls on arsenic speciation and zonation

A. P. Deditius, X. Yao, F. Xia, J. Brugger, Y. Xing, B. E. Etschmann, A. Suvorova, M. P. Roberts and C. M. Kewish
Geochemical perspectives letters, Vol.38, pp.53-59
2026
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CC BY-NC-ND V4.0 Open Access

Abstract

Zoning and speciation of arsenic (As) in pyrite are used to infer changes in the chemical composition of hydrothermal fluids and conditions of ore deposit formation. Yet, the processes controlling the distribution and oxidation state of As during pyrite formation are poorly understood. We report the results of experiments designed to test the capacity of pyrite to record changes in fluid composition under dynamic reaction conditions. When pyrite seeds were exposed alternately to As-bearing and As-free fluids, concentric As-rich (≤6.0 wt. % of As1−) and As-free pyrite overgrowths formed when native S was used as the sulfur source. In contrast, a sodium thiosulfate source produced randomly oriented aggregates of concentrically zoned microparticulate (∼1 μm) As-bearing pyrite (<1.5 wt. % of As2+/3+), failing to record the changes of fluid composition. We demonstrate that by controlling H2S(aq) availability, the source of sulfur affects the degree of pyrite supersaturation under conditions relevant to natural hydrothermal systems, which controls the nucleation rate, crystal growth, As uptake, As oxidation state, and consequently, the ability of pyrite to record individual fluid pulses. This sulfur source effect has significant implications for metal incorporation into pyrite and understanding of the formation of many ore deposits.

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