18:15 〜 19:30
[BPT23-P02] 西オーストラリア・ピルバラクラトンの海洋底玄武岩中の黄鉄鉱四種硫黄同位体比から制約する太古代海底下の微生物活動
Microbial sulfate reduction is one of the most ubiquitous metabolisms on Earth [Canfield, 1998]. In modern environment, it is well known that microbial sulfate reduction takes place below seafloor [e.g. Kallmeyer et al., 2012]. Aoyama et al. [2014] showed microbial sulfate reduction takes place not only in quiescent seafloor (i.e. non-hydrothermal), but also in active hydrothermal system. On the other hand, the oldest evidence of microbial sulfate reduction has been reported from ca. 3.5 Ga Dresser Formation, Western Australia by using quadruple sulfur stable isotopes analyses of sulfate and sulfide minerals related to hydrothermal environment [Ueno et al., 2008; Shen et al., 2009]. However, the isotopic compositions of sulfides and sulfate minerals through history show small isotopic fractionation (~20‰) before the rise of oxygen (c. 2450 Ma), possibly because of low sulfate concentration in the Archean seawater (<200 μM) [Habicht et al., 2002]. Microbial sulfate reduction below Archean seafloor might have yield larger sulfur isotopic fractionation owing to enhanced sulfate concentration. In order to test this scenario, we analyzed quadruple sulfur isotopic compositions of pyrite grains (from 10 to 40 μg) of seafloor basalts. For studying isotopic variation within sample, we used newly developed micro-fluorination technique.
The observed variations within each rock have positive correlations between the d34S and D33S, and negative correlations between the d34S and D36S, suggesting these trends are derived from mixing or fractionation. Pyrite within silica dykes penetrating seafloor basalts, which are the most plausible end-member within pyrite in basalts, however, cannot explain the observed variations. On the other hand, the slope of the observed D36S/ D33S (-9.3) and large variations within small volume rocks (~10‰) suggest microbial sulfate reduction took place in Archean hydrothermal system. The observed intensive d34S depletions only in Unit-I, and mass dependent compositions imply the substrate sulfate was different from Archean seawater suggested by bedded barite in upper part of the Unit-I. Thus the Archean hydrothermal system may have host microbial activity by enhanced sulfate.
The observed variations within each rock have positive correlations between the d34S and D33S, and negative correlations between the d34S and D36S, suggesting these trends are derived from mixing or fractionation. Pyrite within silica dykes penetrating seafloor basalts, which are the most plausible end-member within pyrite in basalts, however, cannot explain the observed variations. On the other hand, the slope of the observed D36S/ D33S (-9.3) and large variations within small volume rocks (~10‰) suggest microbial sulfate reduction took place in Archean hydrothermal system. The observed intensive d34S depletions only in Unit-I, and mass dependent compositions imply the substrate sulfate was different from Archean seawater suggested by bedded barite in upper part of the Unit-I. Thus the Archean hydrothermal system may have host microbial activity by enhanced sulfate.