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汞同位素特征作为纽因特里亚汞矿汞循环示踪剂。

Mercury isotope signatures as tracers for Hg cycling at the New Idria Hg mine.

机构信息

Soil Chemistry Group, Institute of Biogeochemistry and Pollutant Dynamics, ETH Zurich , Switzerland.

出版信息

Environ Sci Technol. 2013 Jun 18;47(12):6137-45. doi: 10.1021/es305245z. Epub 2013 May 28.

Abstract

Mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes provides a new tool for tracing Hg in contaminated environments such as mining sites, which represent major point sources of Hg pollution into surrounding ecosystems. Here, we present Hg isotope ratios of unroasted ore waste, calcine (roasted ore), and poplar leaves collected at a closed Hg mine (New Idria, CA, U.S.A.). Unroasted ore waste was isotopically uniform with δ(202)Hg values from -0.09 to 0.16‰ (± 0.10‰, 2 SD), close to the estimated initial composition of the HgS ore (-0.26‰). In contrast, calcine samples exhibited variable δ(202)Hg values ranging from -1.91‰ to +2.10‰. Small MIF signatures in the calcine were consistent with nuclear volume fractionation of Hg isotopes during or after the roasting process. The poplar leaves exhibited negative MDF (-3.18 to -1.22‰) and small positive MIF values (Δ(199)Hg of 0.02 to 0.21‰). Sequential extractions combined with Hg isotope analysis revealed higher δ(202)Hg values for the more soluble Hg pools in calcines compared with residual HgS phases. Our data provide novel insights into possible in situ transformations of Hg phases and suggest that isotopically heavy secondary Hg phases were formed in the calcine, which will influence the isotope composition of Hg leached from the site.

摘要

汞同位素的质量依赖分馏(MDF)和质量独立分馏(MIF)为追踪矿区等污染环境中的汞提供了一种新工具,矿区是汞污染进入周围生态系统的主要点源。本研究采集了美国加利福尼亚州纽因特利亚封闭汞矿区的原矿废物、烧矿(经焙烧的矿石)和杨树叶片,分析了其汞同位素比值。原矿废物的δ(202)Hg 值在-0.09 至 0.16‰(±0.10‰,2 SD)之间保持同位素均一性,接近估算的 HgS 矿石初始组成(-0.26‰)。相比之下,烧矿样品的 δ(202)Hg 值变化范围较大,为-1.91‰至+2.10‰。烧矿中存在较小的 MIF 特征,这与焙烧过程中或之后汞同位素的核体积分馏一致。杨树叶片表现出负的 MDF(-3.18 至-1.22‰)和较小的正 MIF 值(Δ(199)Hg 为 0.02 至 0.21‰)。连续提取结合汞同位素分析表明,烧矿中更易溶解的汞库的 δ(202)Hg 值高于残余 HgS 相。我们的数据为 Hg 相的可能原位转化提供了新的见解,并表明在烧矿中形成了同位素较重的次生 Hg 相,这将影响从矿区浸出的汞的同位素组成。

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