首页> 外文期刊>Environmental Science & Technology >The 'Degradative' and 'Biological' Pumps Controls on the Atmospheric Deposition and Sequestration of Hexachlorocyclohexanes and Hexachlorobenzene in the North Atlantic and Arctic Oceans
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The 'Degradative' and 'Biological' Pumps Controls on the Atmospheric Deposition and Sequestration of Hexachlorocyclohexanes and Hexachlorobenzene in the North Atlantic and Arctic Oceans

机译:北大西洋和北冰洋六氯环己烷和六氯苯的大气沉积和固存的“降解”和“生物”泵控制

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摘要

The cycling of hexachlorobenzene (HCB) and hexachlorocyclohexanes (HCHs) has been studied in the North Atlantic and Arctic Ocean. Concentrations of HCHs and HCB were measured simultaneously in the atmosphere (gas and aerosol phases), seawater (dissolved and particulate phases), and phytoplankton. The atmospheric concentrations of HCHs decrease during transport over the Greenland Current with estimated e-folding times of 1.6 days, a trend not observed for HCB. This strong decrease in atmospheric concentrations of HCH is consistent with the estimated atmospheric depositional fluxes driven by the air-water disequilibrium. The removal of HCHs from the surface ocean by the degradative pump due to hydrolysis and microbial degradation and by the biological pump due to settling of particle-associated HCHs are estimated; the removal fluxes are within a factor of 2 of the atmospheric inputs for most sampling events, suggesting an important role of the degradative pump in the overall oceanic sink of HCHs. Conversely, the lack of degradation of HCB in surface waters and its relatively low hydrophobicity imply a lack of effective removal processes, consistent with the observed air and water concentrations close to equilibrium. This work is the first that estimates the relative importance of the biological and degradative pumps on the atmospheric deposition of the less persistent organic pollutants and points out the need for further research for quantifying the magnitude of degradative processes in the environment.
机译:在北大西洋和北冰洋已经研究了六氯苯(HCB)和六氯环己烷(HCH)的循环。在大气(气相和气溶胶相),海水(溶解相和颗粒相)和浮游植物中同时测量了六氯环己烷和六氯苯的浓度。在格陵兰洋流上运输期间,六氯环己烷的大气浓度下降,估计电子折叠时间为1.6天,而六氯代苯没有发现这一趋势。六氯环己烷大气浓度的这种强烈下降与空气-水不平衡驱动的估计的大气沉积通量相一致。估计由于水解和微生物降解而由降解泵和由于与颗粒有关的六氯环己烷的沉降而由生物泵从地表海洋中去除六氯环己烷的情况;对于大多数采样事件而言,去除通量在大气输入的2倍以内,这表明降解泵在六氯环己烷的整个海洋汇中起着重要作用。相反,地表水中六氯代苯缺乏降解,且其疏水性相对较低,这意味着缺乏有效的去除工艺,这与观察到的空气和水的浓度接近平衡相一致。这项工作是第一个估算生物和降解泵对持久性较低的有机污染物在大气中沉积的相对重要性的工作,并指出需要进一步研究以量化环境中降解过程的数量。

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  • 来源
    《Environmental Science & Technology》 |2013年第13期|7195-7203|共9页
  • 作者单位

    Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research-Spanish Council for Scientific Research (IDAEA-CSIC), Jordi Girona 18-26, Barcelona 08034, Catalunya, Spain;

    Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research-Spanish Council for Scientific Research (IDAEA-CSIC), Jordi Girona 18-26, Barcelona 08034, Catalunya, Spain;

    Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research-Spanish Council for Scientific Research (IDAEA-CSIC), Jordi Girona 18-26, Barcelona 08034, Catalunya, Spain;

    Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research-Spanish Council for Scientific Research (IDAEA-CSIC), Jordi Girona 18-26, Barcelona 08034, Catalunya, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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