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多环芳烃在东海沉积物-孔隙水中的分布:存在、分配和扩散。

Polycyclic aromatic hydrocarbons in sediment-porewater system from the East China Sea: Occurrence, partitioning, and diffusion.

机构信息

State Environmental Protection Key Laboratory of Coastal Ecosystem, National Marine Environmental Monitoring Center, Dalian, 116023, China; Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Institute of Atmospheric Sciences, Department of Environmental Science and Engineering, Fudan University, Shanghai, 200433, China.

College of Marine Ecology and Environment, Shanghai Ocean University, Shanghai, 201306, China.

出版信息

Environ Res. 2022 Jun;209:112755. doi: 10.1016/j.envres.2022.112755. Epub 2022 Feb 5.

Abstract

The distribution, partitioning behavior, and diffusion of polycyclic aromatic hydrocarbons (PAHs) within sediment-porewater system were determined in two cores obtained from the Min-Zhe coastal mud of the East China Sea (ECS). Depth profiles of apparently dissolved PAH levels exhibited greater variabilities, with their elevated levels at depth and a high abundance of two-to three-ring PAHs observed. These distribution and composition patterns were inconsistent with the corresponding sediment PAHs, indicating differences in controlling factors for PAHs present in the system. In addition to compound's hydrophobicity, low detection of heavier PAHs in porewater was possibly correlated with the sediment transport process, as indicated by a relatively high weathering ratio in southern Min-Zhe coastal mud. PAH sorption affinity to the collected core sediments exhibited a generally decreasing trend downcore, as expressed by sediment-porewater partition coefficients. This was consistent with the higher content of porewater PAHs in deep core sediment. The established sediment total organic carbon (TOC)-porewater partitioning profiles in cores were predicted with amorphous organic carbon (AOC)-, coal tar-, and TOC-based distribution models, suggesting a dominant nonlinear sorption of PAHs to AOC. Through activity determinations, PAH diffusion within porewater was elucidated, with significant upward and downward mass transfer for PAHs occurring in both cores. The upward diffusion in the core collected from northern Min-Zhe coastal mud was in significant association with sediment TOC. This suggests that sediment TOC (especially AOC)-desorption of lighter PAHs into porewater, and therefore the possibility of their participation in environmental cycling. Baseline toxicity potential and toxic unit calculations indicated a relatively low exposure risk for benthic organisms to porewater PAHs.

摘要

多环芳烃(PAHs)在沉积物-水孔隙系统中的分布、分配行为和扩散情况在取自东海闽浙沿岸泥质区的两个柱状沉积物中得到了确定。明显溶解态 PAH 水平的深度分布表现出更大的变异性,其在深度上的升高水平和大量的二至三环 PAH 含量丰富。这些分布和组成模式与相应的沉积物 PAHs 不一致,表明系统中存在的 PAHs 受到不同控制因素的影响。除了化合物的疏水性之外,水孔隙中较重 PAHs 的低检测可能与沉积物输运过程有关,这一点可以从闽浙南部沿岸泥质较高的风化比值得到证实。PAH 对采集的柱状沉积物的吸附亲和力呈向下逐渐降低的趋势,表现为沉积物-水分配系数的降低。这与深部柱状沉积物中更高的水孔隙 PAHs 含量一致。在两个柱状沉积物中建立的总有机碳(TOC)-水分配轮廓与无定形有机碳(AOC)、煤焦油和 TOC 基分布模型预测的结果一致,这表明 PAH 对 AOC 具有主导的非线性吸附。通过活性测定,阐明了水孔隙中 PAH 的扩散,两个柱状沉积物中均发生了显著的向上和向下 PAH 质量转移。从闽浙北部沿岸泥质区采集的柱状沉积物中向上扩散与沉积物 TOC 密切相关。这表明沉积物 TOC(特别是 AOC)-将较轻的 PAHs 解吸到水孔隙中,因此它们有可能参与环境循环。基于毒性潜力和毒性单位的计算表明,底栖生物对水孔隙 PAHs 的暴露风险相对较低。

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