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Mercury concentrations in Irish headwater lake catchments

机译:爱尔兰上游水域流域的汞含量

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An estimated 215,000 tonnes of mercury (Hg) have been emitted to the atmosphere from anthropogenic sources since the nineteenth century, igniting widespread environmental monitoring owing to its toxicity. The environmental fate of Hg is strongly determined by catchment characteristics, especially soil organic matter. In this study, concentrations and pools of Hg were determined for lakes and soils in upland peat-dominated catchments in Ireland to assess controls of aquatic Hg and soil response to changes in emissions. Headwater lakes in upland coastal regions were surveyed for water chemistry and total Hg (THg) during spring 2008. In addition, a sub-set of lakes (n = 5) were repeatedly sampled during 2009-2011, and their surface soils collected for Hg analysis, including a short (30 cm) peat core to assess temporal Hg fluxes using radiometric Pb-210 dating. Peat cores indicated a significant decrease in Hg deposition since the 1980s, in broad agreement with other 'background' regions. Total Hg was correlated with total organic carbon (TOC) in the survey and intensive study lakes (r = 0.70 and 0.45), indicative of the strong affinity of Hg to organic matter. At the intensive lakes, monomethylmercury (MMHg) made up 3.3 % of mean THg and exhibited a positive correlation with total SO4 (2-) (r = 0.55). Further, both THg and MMHg were significantly correlated with conductivity (r = 0.48 and 0.54, respectively) potentially owing to marine inputs, and negatively correlated with pH (r = -0.59 and -0.56 respectively). Significant differences in THg (and MMHg) were observed between the five lakes, the highest concentrations (4.45 and 0.16 ng L-1, respectively) tended to be associated with TOC in lakes and occurred at sites in the northwest, characterized by higher levels of soil organic matter (peat) and soil moisture relative to the other sites. In contrast, surface soil pools of THg ranged between 13.6 and 20.8 mu g m(-2) across study sites and did not vary significantly, but were typical of global background regions. Nonetheless, the organic rich soils that dominate Ireland are a natural sink for THg, and peat harvesting for energy production may release long-term stores of Hg from deeper soil layers.
机译:自19世纪以来,估计已从人为源向大气排放了215,000吨汞(Hg),由于其毒性,引发了广泛的环境监测。汞的环境命运很大程度上取决于集水特征,尤其是土壤有机质。在这项研究中,确定了爱尔兰高地泥炭为主的流域中湖泊和土壤中汞的浓度和池,以评估对水生汞的控制以及土壤对排放变化的响应。在2008年春季期间,对陆地高地沿海地区的源头湖泊进行了水化学和总Hg(THg)的调查。此外,在2009-2011年期间重复采样了一个子集(n = 5),并收集了其表层土壤中的Hg分析,包括一个短的(30厘米)泥炭芯,使用放射性Pb-210测年法评估时间汞通量。泥炭岩心表明,自1980年代以来,汞的沉积显着减少,这与其他“背景”区域基本一致。在调查和深入研究的湖泊中,总汞与总有机碳(TOC)相关(r = 0.70和0.45),表明汞对有机物具有很强的亲和力。在集约化湖泊中,一甲基汞(MMHg)占平均THg的3.3%,并且与总SO4(2-)呈正相关(r = 0.55)。此外,THg和MMHg都可能与海洋输入引起的电导率显着相关(分别为r = 0.48和0.54),而与pH呈负相关(分别为r = -0.59和-0.56)。在五个湖泊之间观察到THg(和MMHg)存在显着差异,最高浓度(分别为4.45和0.16 ng L-1)往往与湖泊中的TOC有关,并发生在西北部地区,其特征是较高的相对于其他地点的土壤有机质(豌豆)和土壤水分。相比之下,不同研究地点的THg表层土壤池范围在13.6和20.8μg m(-2)之间,变化不大,但是全球背景区域的典型特征。但是,在爱尔兰占主导地位的富含有机物的土壤是THg的天然汇,收获能源以生产泥炭可能会释放深层土壤中的Hg长期储存。

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