4.7 Article

Clumped isotope signatures of methane-derived authigenic carbonate presenting equilibrium values of their formation temperatures

期刊

EARTH AND PLANETARY SCIENCE LETTERS
卷 512, 期 -, 页码 207-213

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.epsl.2019.02.005

关键词

clumped isotopes; cold seep; authigenic carbonate; oxygen isotope; AOM rate; Japan Sea

资金

  1. METI (Ministry of Economy, Trade and Industry, Japan)
  2. JSPS fellowship [P18113]
  3. Austrian Science Fund (FWF) [P18113] Funding Source: Austrian Science Fund (FWF)

向作者/读者索取更多资源

The chemical and stable isotopic composition of methane-derived authigenic carbonate (MDAC) can be used to document paleoclimate and biogeochemical information in methane cold seeps, such as temperature records determined through clumped isotope (Delta(47)) analyses. Previous investigations of MDACs, however, have noted isotopic disequilibrium values, limiting the application of Delta(47 )signatures as a proxy for the formation temperature of carbonates at present and former gas seep sites. Here we measured 49 MDAC samples collected from 5 areas along the Eastern margin of the Japan Sea and the northwest Pacific region of Japan. All samples present equilibrium Delta(47 )signatures with respect to seafloor temperatures at the time of precipitation, and the results do not appear to be influenced by the Mg content, mineralogy or mixing effect. The pore water delta O-18 values estimated by the Delta(47) thermometer reveal that most of these MDACs formed during glacial and/or hydrate destabilization periods. While our new data shows equilibrium Delta(47) values, the results do not discount the possibility that disequilibrium observed in previous studies could possibly be associated with extremely rapid rates of anaerobic oxidation of methane. Relevant potential mechanisms are discussed. Further investigations are crucial to clarify the utility of Delta(47) in MDACs as a novel proxy for constraining the modern/ancient methane seep environment. This proxy also offers insights into formation and dissociation processes of gas hydrate, a potential energy resource in the future. (C) 2019 Elsevier B.V. All rights reserved.

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