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平衡式被动采样在多瑙河沉积物中分析孔隙水和疏水性有机污染物可及浓度分布的应用。

Application of equilibrium passive sampling to profile pore water and accessible concentrations of hydrophobic organic contaminants in Danube sediments.

机构信息

Masaryk University, Faculty of Science, Centre RECETOX, Kamenice 753/5, 625 00, Brno, Czech Republic.

Masaryk University, Faculty of Science, Centre RECETOX, Kamenice 753/5, 625 00, Brno, Czech Republic.

出版信息

Environ Pollut. 2020 Dec;267:115470. doi: 10.1016/j.envpol.2020.115470. Epub 2020 Aug 27.

Abstract

Total concentrations of hydrophobic organic contaminants (HOCs) in sediment present a poor quality assessment parameter for aquatic organism exposure and environmental risk because they do not reflect contaminant bioavailability. The bioavailability issue of HOCs in sediments can be addressed by application of multi-ratio equilibrium passive sampling (EPS). In this study, riverbed sediment samples were collected during the Joint Danube Survey at 9 locations along the Danube River in 2013. Samples were ex-situ equilibrated with silicone passive samplers. Desorption isotherms were constructed, yielding two endpoints: pore water (C) and accessible (C) concentration of polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs) and polybrominated diphenyl ethers in sediment. C concentrations of DDT and its breakdown products exhibited elevated levels in the low Danube, with the maximum in the river delta. Other investigated HOCs did not show any clear spatial trends along the river, and only a moderate C variability. C in sediment ranged from 10 to 90% of the total concentration in sediment. C was compared with freely dissolved concentration in the overlaying surface water, measured likewise by passive sampling. The comparison indicated potential compound release from sediment to the water phase for PAHs with less than four aromatic rings, and for remaining HOCs either equilibrium between sediment and water, or potential compound deposition in sediment. Sorption partition coefficients of HOC to organic carbon correlated well with octanol-water partition coefficients (K), showing stronger sorption of PAHs to sediment than that of PCBs and OCPs having equal logK. Comparison of C values with European environmental quality standards indicated potential exceedance for hexachlorobenzene, fluoranthene and benzo[a]pyrene at several sites. The study demonstrates the utility of passive sampling as an innovative approach for risk-oriented monitoring of HOCs in river catchments.

摘要

疏水性有机污染物(HOCs)在沉积物中的总浓度是评估水生生物暴露和环境风险的一个较差参数,因为它们不能反映污染物的生物可利用性。可以通过应用多比率平衡被动采样(EPS)来解决沉积物中 HOCs 的生物可利用性问题。在这项研究中,于 2013 年在多瑙河联合调查期间在多瑙河沿线的 9 个地点采集了河床沉积物样本。样本与硅酮被动采样器进行了原位平衡。构建了解吸等温线,得出了两个端点:多氯联苯(PCBs)、有机氯农药(OCPs)、多环芳烃(PAHs)和多溴二苯醚在沉积物中的孔隙水(C)和可及(C)浓度。滴滴涕及其分解产物的 C 浓度在多瑙河下游呈现升高的水平,在河口处达到最大值。其他研究的 HOCs 沿河流没有显示出任何明显的空间趋势,只有中等程度的 C 变异性。C 在沉积物中的范围为 10%至 90%,与沉积物中的总浓度相比。C 与同样通过被动采样测量的上覆地表水的自由溶解浓度进行了比较。该比较表明,对于少于四个芳环的 PAHs,存在化合物从沉积物向水相释放的潜力,对于其余的 HOCs,要么是沉积物和水之间的平衡,要么是化合物在沉积物中的沉积。HOC 与有机碳的吸附分配系数与辛醇-水分配系数(K)密切相关,表明 PAHs 对沉积物的吸附比具有相同 logK 的 PCB 和 OCP 更强。将 C 值与欧洲环境质量标准进行比较表明,在几个地点存在六氯苯、荧蒽和苯并[a]芘可能超标。该研究表明,被动采样作为一种面向风险的河流流域 HOCs 监测的创新方法具有实用性。

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