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Methylation of Mercury by Bacteria Exposed to Dissolved, Nanoparticulate, and Microparticulate Mercuric Sulfides

Mercury(编程语言) 甲基汞 化学 环境化学 纳米颗粒 硫酸盐还原菌 硫化物 生物利用度 溶解有机碳 硫酸盐 无机化学 有机质 细菌 美爵酒店 生物累积 化学工程 有机化学 地质学 古生物学 工程类 程序设计语言 分析化学(期刊) 生物 生物信息学 计算机科学
作者
Tong Zhang,Bojeong Kim,Clément Levard,Brian C. Reinsch,Gregory Victor Lowry,Marc A. Deshusses,Heileen Hsu‐Kim
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:46 (13): 6950-6958 被引量:291
标识
DOI:10.1021/es203181m
摘要

The production of the neurotoxic methylmercury in the environment is partly controlled by the bioavailability of inorganic divalent mercury (Hg(II)) to anaerobic bacteria that methylate Hg(II). In sediment porewater, Hg(II) associates with sulfides and natural organic matter to form chemical species that include organic-coated mercury sulfide nanoparticles as reaction intermediates of heterogeneous mineral precipitation. Here, we exposed two strains of sulfate-reducing bacteria to three forms of inorganic mercury: dissolved Hg and sulfide, nanoparticulate HgS, and microparticulate HgS. The bacteria cultures exposed to HgS nanoparticles methylated mercury at a rate slower than cultures exposed to dissolved forms of mercury. However, net methylmercury production in cultures exposed to nanoparticles was 6 times greater than in cultures treated with microscale particles, even when normalized to specific surface area. Furthermore, the methylation potential of HgS nanoparticles decreased with storage time of the nanoparticles in their original stock solution. In bacteria cultures amended with nano-HgS from a 16 h-old nanoparticle stock, 6-10% of total mercury was converted to methylmercury after one day. In contrast, 2-4% was methylated in cultures amended with nano-HgS that was aged for 3 days or 1 week. The methylation of mercury derived from nanoparticles (in contrast to the larger particles) would not be predicted by equilibrium speciation of mercury in the aqueous phase (<0.2 μm) and was possibly caused by the disordered structure of nanoparticles that facilitated release of chemically labile mercury species immediately adjacent to cell surfaces. Our results add new dimensions to the mechanistic understanding of mercury methylation potential by demonstrating that bioavailability is related to the geochemical intermediates of rate-limited mercury sulfide precipitation reactions. These findings could help explain observations that the "aging" of mercury in sediments reduces its methylation potential and provide a basis for assessing and remediating methylmercury hotspots in the environment.

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