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Nickel Phase Partitioning and Toxicity in Field-Deployed Sediments

机译:镍在野外沉积物中的分配和毒性

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摘要

The pool of bioavailable metal in sediments can be much smaller than total metal concentration due to complexation and precipitation with ligands. Metal bioavailability and toxicity in sediment is often predicted from models of simultaneous extracted metal and acid volatile sulfide (SEM-AVS); however, studies of the applicability of these models for Ni-contaminated sediments have been conducted primarily in laboratory settings. We investigated the utility of the SEM-AVS models under field conditions: Five lotic sediments with a range of sulfide and organic carbon contents were amended with four concentrations of Ni, deployed in streams for eight weeks, and examined for colonizing macroinvertebrates. After four weeks, colonizing macroinvertebrates showed a strong negative response to the Ni-treated sediments and SEM-AVS models of bioavailability differentiated between toxic and nontoxic conditions. By Week 8, relationships deteriorated between colonizing macroinvertebrates and SEM-AVS model predictions. Total Ni in the sediment did not change through time; however, Ni partitioning shifted from being dominated by organic cabon at deployment to associations with Fe and Mn, Combined geochemical and toxicity results suggest that Fe and Mn oxides in surface sediments resulted in Ni being less available to biota. This implies that current SEM-AVS models may overestimate bioavailable Ni in sediments with oxic surface layers and sufficient Fe and Mn.
机译:由于与配体的络合和沉淀,沉积物中的生物可利用金属库可能比总金属浓度小得多。通常根据同时提取的金属和酸挥发性硫化物(SEM-AVS)的模型预测沉积物中金属的生物利用度和毒性。然而,这些模型对镍污染沉积物的适用性研究主要是在实验室环境中进行的。我们在野外条件下研究了SEM-AVS模型的实用性:用4种浓度的Ni修正了5种具有一定范围的硫化物和有机碳含量的渗碳沉积物,并在水流中部署了8周,并检查了其对大型无脊椎动物的定殖。四周后,定居的大型无脊椎动物对经镍处理的沉积物表现出强烈的负面反应,并且在有毒和无毒条件下区分生物利用度的SEM-AVS模型。到第8周时,定居的大型无脊椎动物和SEM-AVS模型预测之间的关系恶化。沉积物中的总镍没有随时间变化。然而,镍的分配从在部署时被有机碳控制为主,转变为与铁和锰的结合。综合的地球化学和毒性结果表明,表面沉积物中的铁和锰氧化物导致镍难以被生物利用。这意味着当前的SEM-AVS模型可能会高估含氧表面层和足够的铁和锰的沉积物中的生物利用镍。

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  • 来源
    《Environmental Science & Technology》 |2011年第13期|p.5798-5805|共8页
  • 作者单位

    School of Natural Resources & Environment, University of Michigan, 440 Church St., Ann Arbor, Michigan 48109, United States;

    School of Natural Resources & Environment, University of Michigan, 440 Church St., Ann Arbor, Michigan 48109, United States;

    Department of Earth & Environmental Sciences, Wright State University, 3640 Colonel Glenn Hwy., Dayton, Ohio 45435,United States;

    Nickel Producers Environmental Research Association (NiPERA), 2605 Meridian Parkway, Suite 121, Durham, North Carolina 27713,United States;

    Nickel Producers Environmental Research Association (NiPERA), 2605 Meridian Parkway, Suite 121, Durham, North Carolina 27713,United States;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-17 14:03:45

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