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Sulfidity controls molybdenum isotope fractionation into euxinic sediments: Evidence from the modern Black Sea

机译:硫化物控制钼同位素分馏为富氧沉积物:现代黑海的证据

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摘要

Molybdenum (Mo) isotope fractionation has recently been introduced as a new proxy in oceanography and biogeochemistry. It is therefore fundamental to understand the processes controlling Mo partitioning into modern marine environments. This study identifies the availability of dissolved sulfide as the dominant control on overall Mo removal from the water column in euxinic systems. Mo isotopic composition of surface sediments from different localities of the Black Sea demonstrates complete fixation of Mo only below 400 m water depth, above a critical concentration of 11 µmol l–1 aqueous hydrogen sulfide in the bottom water. The Mo isotopic composition of these sediments reflects the homogeneous seawater isotopic composition of 2.3. In contrast, significant Mo isotope fractionation into less euxinic sediments is evident at shallower depths in the Black Sea, as well as in temporarily euxinic deeps of the Baltic Sea, consistent with the observed lower maximum sulfide concentrations in the respective water columns. Therefore, Mo isotope signatures in the modern Black Sea constrain the processes responsible for global Mo removal from the ocean by euxinic sediments. Furthermore, models of past ocean anoxia reconstruction have to consider that the seawater Mo isotopic composition is not per se archived in euxinic sediments.
机译:钼(Mo)同位素分级法最近被引入 作为海洋学和生物地球化学的新代理。因此, 的基本知识是了解将Mo分区 控制到现代海洋环境的过程。这项研究确定了溶解性硫化物的有效性 作为优生系统水柱中总Mo去除量的主要控制因素。来自黑 海不同地区的地表沉积物的Mo同位素组成 证明仅在低于临界浓度以上400 m水 深度以下,Mo才能完全固定底部水中的11 µmol l –1 硫化氢水溶液。这些沉积物的Mo同位素 组成反映了2.3的均质海水 同位素组成。相比之下,在黑海的 浅水深处,以及暂时的euxinic的深处 中,明显的Mo同位素分馏成少量的低油质沉积物是明显的。波罗的海,与在各个水柱中观测到的较低的最高 硫化物浓度一致。因此,现代黑海中的 Mo同位素特征限制了 过程,该过程负责通过 共生沉积物从海洋中整体去除Mo。此外,过去的海洋缺氧 重建模型必须考虑到,海水Mo同位素 的组成本身并没有储存在富氧沉积物中。

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  • 来源
    《Geology 》 |2008年第10期| 775-778| 共4页
  • 作者单位

    Institute of Geological Sciences, Isotope Geology Group, University of Bern, CH-3012 Bern, Switzerland;

    Institute of Geological Sciences, Isotope Geology Group, University of Bern, CH-3012 Bern, Switzerland;

    Leibniz Institute for Baltic Sea Research, Marine Geochemistry Group, Warnemünde, Germany, and Max Planck Institute for Marine Microbiology, Biogeochemistry Department, Bremen, Germany;

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