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自1986年以来,苏必利尔湖已减少了90%以上的六氯环己烷农药负荷。

Lake Superior Has Lost over 90% of Its Pesticide HCH Load since 1986.

作者信息

Bidleman Terry F, Backus Sean, Dove Alice, Lohmann Rainer, Muir Derek, Teixeira Camilla, Jantunen Liisa

机构信息

Department of Chemistry, Umeå University, Umeå, SE-90187, Sweden.

Great Lakes Ecosystem Management Section, Environment and Climate Change Canada, Burlington, Ontario L7R 4A6, Canada.

出版信息

Environ Sci Technol. 2021 Jul 20;55(14):9518-9526. doi: 10.1021/acs.est.0c07549. Epub 2021 Apr 7.

Abstract

The time trend of α- and γ-hexachlorocyclohexane (HCH) isomers in Lake Superior water was followed from 1986 to 2016, the longest record for any persistent organic pollutant (POP) in Great Lakes water. Dissipation of α-HCH and γ-HCHs was first order, with halving times () of 5.7 and 8.5 y, respectively. Loss rates were not significantly different starting a decade later (1996-2016). Concentrations of β-HCH were followed from 1996-2016 and dissipated more slowly ( = 16 y). In 1986, the lake contained an estimated 98.8 tonnes of α-HCH and 13.2 tonnes of γ-HCH; by 2016, only 2.7% and 7.9% of 1986 quantities remained. Halving times of both isomers in water were longer than those reported in air, and for γ-HCH, they were longer in water than those reported in lake trout. Microbial degradation was evident by enantioselective depletion of (+)α-HCH, which increased from 1996 to 2011. Volatilization was the main removal process for both isomers, followed by degradation (hydrolytic and microbial) and outflow through the St. Mary's River. Sedimentation was minor. Major uncertainties in quantifying removal processes were in the two-film model for predicting volatilization and in microbial degradation rates. The study highlights the value of long-term monitoring of chemicals in water to interpreting removal processes and trends in biota.

摘要

1986年至2016年期间,对苏必利尔湖水中α-六氯环己烷(α-HCH)和γ-六氯环己烷(γ-HCH)异构体的时间趋势进行了跟踪研究,这是五大湖水中任何持久性有机污染物(POP)最长的记录。α-HCH和γ-HCH的消散符合一级动力学,半衰期分别为5.7年和8.5年。十年后(1996 - 2016年)损失率没有显著差异。1996年至2016年期间对β-HCH的浓度进行了跟踪,其消散速度较慢(半衰期 = 16年)。1986年,该湖中估计含有98.8吨α-HCH和13.2吨γ-HCH;到2016年,仅分别剩余1986年含量的2.7%和7.9%。两种异构体在水中的半衰期均长于空气中报告的半衰期,对于γ-HCH,其在水中的半衰期长于湖鳟中报告的半衰期。对映体选择性消耗(+)α-HCH表明存在微生物降解,这种消耗从1996年到2011年有所增加。挥发是两种异构体的主要去除过程,其次是降解(水解和微生物降解)以及通过圣玛丽河的流出。沉降作用较小。量化去除过程的主要不确定性在于预测挥发的双膜模型和微生物降解速率。该研究强调了对水中化学物质进行长期监测对于解释生物群中的去除过程和趋势的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1e/8296669/fd4db9e84553/es0c07549_0001.jpg

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