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威斯康星州北部一个以湿地为主的湖泊中甲基汞的来源。

Sources of methylmercury to a wetland-dominated lake in northern Wisconsin.

作者信息

Watras C J, Morrison K A, Kent A, Price N, Regnell O, Eckley C, Hintelmann H, Hubacher T

机构信息

Wisconsin Department of Natural Resources, Madison, Wisconsin, USA.

出版信息

Environ Sci Technol. 2005 Jul 1;39(13):4747-58. doi: 10.1021/es040561g.

Abstract

Several lines of evidence suggest that wetlands may be a major source of methylmercury (MeHg) to receiving waters, perhaps explaining the strong correlation between concentrations of waterborne MeHg and dissolved organic carbon (DOC) in regions such as northern Wisconsin. We evaluated the relative importance of wetland export in the MeHg budget of a wetland-dominated lake in northern Wisconsin using mass balance. Channelized runoff from a large headwater wetland was the major source of water and total mercury (HgT) to the lake during the study period. The wetland also exported MeHg in high concentrations (0.2-0.8 ng L(-1)), resulting in an export rate similar to those reported for other northern wetlands (ca. 0.3 microg MeHg m(-2) y(-1)). Yet, based on intensive sampling during 2002, the mass of MeHg that accumulated in the lake during summer was an order of magnitude greater than the export of MeHg from the wetland to the lake. Hence, a large in-lake source of MeHg is inferred from the mass balance. Most of the accumulated MeHg built-up in anoxic hypolimnetic waters; and the build-up was roughly balanced by losses of inorganic Hg (Hg(II)) implying a chemical transformation within the anoxic water column. An abundance of sulfate-reducing bacteria (SRB) in hypolimnetic waters, established by DNA analysis of the pelagic microbial community, along with a previous report documenting high methylation rates in the hypolimnion of this lake (ca. 10% d(-1)), suggest that this transformation was microbially mediated. These findings indicate that the direct effect of wetland runoff may be outweighed by indirect effects on the lacustrine MeHg cycle, enhancing the load of Hg(II), the activity of SRB, and the retention of MeHg, especially in northern lakes with flushing times longer than six months.

摘要

有几条证据表明,湿地可能是甲基汞(MeHg)进入受纳水体的主要来源,这或许可以解释在威斯康星州北部等地区,水体中甲基汞浓度与溶解有机碳(DOC)之间的强相关性。我们利用质量平衡法评估了湿地输出在威斯康星州北部一个以湿地为主的湖泊甲基汞收支中的相对重要性。在研究期间,来自一个大型源头湿地的渠道化径流是该湖泊水和总汞(HgT)的主要来源。该湿地还以高浓度(0.2 - 0.8 ng L⁻¹)输出甲基汞,其输出速率与其他北方湿地报道的速率相似(约0.3 μg MeHg m⁻² y⁻¹)。然而,根据2002年的密集采样,夏季湖泊中积累的甲基汞质量比湿地向湖泊输出的甲基汞质量大一个数量级。因此,从质量平衡推断湖泊中存在一个很大的甲基汞内源。大部分积累的甲基汞在缺氧的湖下层水体中蓄积;这种蓄积大致与无机汞(Hg(II))的损失相平衡,这意味着在缺氧水柱内发生了化学转化。通过对浮游微生物群落的DNA分析确定,湖下层水体中有大量的硫酸盐还原菌(SRB),同时之前有报告记录该湖泊湖下层的甲基化率很高(约10% d⁻¹),这表明这种转化是由微生物介导的。这些发现表明,湿地径流的直接影响可能被对湖泊甲基汞循环的间接影响所抵消,从而增强了Hg(II)的负荷、SRB的活性以及甲基汞的滞留,特别是在冲洗时间超过六个月的北方湖泊中。

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