Formation of authigenic carbonates contributed by sulfate- and metal-driven anaerobic oxidation of methane in the northern Okinawa Trough, East China Sea

GSA Bulletin Pub Date : 2022-10-27 DOI:10.1130/b36400.1
Lei Liu, H. Guan, Lanfang Xu, Zhilei Sun, N. Wu
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Abstract

Authigenic carbonates of the northern Okinawa Trough have been shown to be contributed by both sulfate- and Fe-driven anaerobic oxidation of methane (SD-AOM and Fe-AOM, respectively); however, the microorganisms involved remain poorly constrained. To better understand the types and roles of microorganisms in specific biological methane oxidation processes, authigenic carbonates collected from the northern Okinawa Trough at water depths between ∼540 m and 700 m were studied using petrographic, mineralogical, elemental, and lipid biomarker analyses. The carbonate minerals were primarily aragonite, high-magnesium calcite, low-magnesium calcite, or dolomite. The extremely low δ13C values of bulk carbonates (−59.2‰), molecular fossils of anaerobic methane oxidizing archaea (ANME; −131‰), and sulfate-reducing bacteria (SRB; −77‰) indicated that the authigenic carbonates formed as products of AOM. Biogenic methane was confirmed to be the main carbon source for all carbonates, whereas bio-degraded oil and hydrothermal input complemented carbon sources, as revealed by the occurrence of unresolved complex mixture, strongly enriched As and Sb, and their correlations with Fe/Al. Combined with enriched δ18O values (as high as +5‰), the methane fluids were suggested to derive from the dissociation of gas hydrates. ANME-2 and a mixture of ANME-1 and ANME-2 were identified for the two calcitic carbonates, respectively, as revealed by their specific biomarker patterns. The relatively higher contents of 13C-depeleted isoprenoids and SRB−related fatty acids, strong Mo enrichment, and biological debris in both calcite- and aragonite-dominated carbonates reflect precipitation driven by SD-AOM in a shallow sulfate-methane transition. For other seep carbonates, low amounts of 13C-depeleted isoprenoids and the near absence of crocetane suggest dominance of the ANME-1 assemblage. The extremely low amounts and non-13C-depleted iso-/anteiso-C15:0 fatty acids (−27‰) in the dolomite-containing carbonates indicate the decoupling of ANME and SRB. These carbonates were most likely formed below or at the bottom of the sulfate-methane transition and included contributions from Fe-AOM, as indicated by the low Mo content, occurrence of dolomite and siderite, and decreased δ56Fe values with increasing Fe/Al ratios.
东海冲绳海槽北部由硫酸盐和金属驱动的甲烷厌氧氧化作用形成自生碳酸盐
冲绳海槽北部的自生碳酸盐被证明是由硫酸盐和铁驱动的甲烷厌氧氧化(分别为SD-AOM和Fe-AOM)贡献的;然而,涉及的微生物仍然很少受到限制。为了更好地了解微生物在特定生物甲烷氧化过程中的类型和作用,我们对冲绳海槽北部水深约540 m至700 m的自生碳酸盐进行了岩石学、矿物学、元素学和脂质生物标志物分析。碳酸盐矿物主要为文石、高镁方解石、低镁方解石或白云石。块状碳酸盐岩δ13C值极低(- 59.2‰),厌氧甲烷氧化古细菌(ANME)分子化石;−131‰),硫酸盐还原菌(SRB;−77‰)表明自生碳酸盐是AOM的产物。生物成因甲烷是所有碳酸盐的主要碳源,而生物降解油和热液输入补充了碳源,这表明存在未解复杂混合物,强富集的as和Sb及其与Fe/Al的相关性。结合富δ18O值(高达+5‰),认为甲烷流体来源于天然气水合物的解离作用。根据其特定的生物标志物模式,分别鉴定出两种碳酸钙的ANME-2和ANME-1和ANME-2的混合物。方解石和文石为主的碳酸盐中相对较高的13c -贫类异戊二烯和SRB -相关脂肪酸含量、强Mo富集和生物碎屑反映了SD-AOM在浅层硫酸盐-甲烷转变中驱动的降水。对于其他渗漏碳酸盐,低含量的13c -贫类异戊二烯和几乎没有鳄鱼烷表明ANME-1组合占主导地位。含白云岩碳酸盐中含量极低且不缺13c的iso-/anteiso-C15:0脂肪酸(- 27‰)表明ANME与SRB存在解耦作用。这些碳酸盐极有可能形成于硫酸盐-甲烷转变的下方或底部,并有Fe- aom的贡献,表现为低Mo含量,白云石和菱铁矿的出现,δ56Fe值随着Fe/Al比值的增加而降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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