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利用鸟粪沉积物中的汞稳定同位素示踪南极罗斯海汞的历史循环

Mercury Stable Isotopes in Ornithogenic Deposits As Tracers of Historical Cycling of Mercury in Ross Sea, Antarctica.

机构信息

†Department of Earth Sciences, University of Toronto, 22 Russell Street, Toronto, Ontario M5S 3B1, Canada.

‡Institute of Polar Environment, School of Earth and Space Sciences, University of Science and Technology of China, Hefei, Anhui 230026, China.

出版信息

Environ Sci Technol. 2015 Jul 7;49(13):7623-32. doi: 10.1021/acs.est.5b00523. Epub 2015 Jun 10.

Abstract

Production of methylmercury (MeHg) in ocean waters and its bioaccumulation in marine organisms are critical processes controlling the fate and toxicity of mercury (Hg). However, these processes are not well understood in the Antarctic, where high levels of MeHg are observed in the subsurface ocean (100-1000 m). We explored the use of Hg stable isotope compositions in historical and modern biological deposits as a new approach for discerning Hg sources and tracing MeHg cycling in the ocean and bioaccumulation in marine biota. We found similar mass independent isotope fractionation (MIF) of Hg between a sediment profile containing historical penguin and seal feces deposits from coastal Antarctica and modern penguin and seal feces, suggesting that penguin and seal feces were the dominant sources of Hg to the sediments at different time periods. Furthermore, sediments dominated by seal feces displayed a significantly lower MIF slope (Δ(199)Hg/Δ(201)Hg) than those dominated by penguin feces despite similar extents of MIF. Since seals forage at greater depths (>400 m) than penguins (<100 m), the high MIF values and lower Δ(199)Hg/Δ(201)Hg in seal feces suggest that a significant fraction of MeHg accumulated by seals was produced in situ in the subsurface ocean from residual inorganic Hg(II) that sank from the euphotic zone after partial photoreduction. Our results suggest that in situ Hg methylation can be an important source of MeHg for marine biota, and Hg isotope compositions in biological archives can be valuable tracers of MeHg cycling.

摘要

在海洋中,甲基汞(MeHg)的生成及其在海洋生物体内的生物累积,是控制汞(Hg)归宿和毒性的关键过程。然而,在南极,由于在次表层海洋(100-1000 米深处)中观测到高浓度的 MeHg,这些过程还不甚清楚。我们探讨了利用汞稳定同位素组成来研究历史和现代生物沉积物,作为一种新方法来辨别汞的来源,追踪海洋中 MeHg 的循环和在海洋生物中的生物累积。我们发现,在含有来自沿海南极洲的历史企鹅和海豹粪便沉积物的沉积剖面中,以及在现代企鹅和海豹粪便中,汞的质量独立同位素分馏(MIF)具有相似性,这表明在不同时期,企鹅和海豹粪便都是沉积物中汞的主要来源。此外,尽管 MIF 的程度相似,但主要由海豹粪便组成的沉积物的 MIF 斜率(Δ(199)Hg/Δ(201)Hg)明显低于主要由企鹅粪便组成的沉积物。由于海豹的觅食深度大于企鹅(>400 米)(<100 米),海豹粪便中较高的 MIF 值和较低的 Δ(199)Hg/Δ(201)Hg 表明,海豹体内积累的大量 MeHg 是由次表层海洋中残留的无机 Hg(II)原位生成的,这些 Hg(II) 是在部分光还原后从真光层下沉的。我们的研究结果表明,原位汞甲基化可能是海洋生物体内 MeHg 的重要来源,生物档案中的汞同位素组成可以作为 MeHg 循环的有价值示踪剂。

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