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基于固相微萃取(SPME)的沉积物中有机污染物被动采样:自由溶解浓度与生物累积的比较。

A passive sampler based on solid phase microextraction (SPME) for sediment-associated organic pollutants: Comparing freely-dissolved concentration with bioaccumulation.

机构信息

Southern California Coastal Water Research Project Authority, 3535 Harbor Boulevard, Suite 110, Costa Mesa, CA 92626, USA.

Southern California Coastal Water Research Project Authority, 3535 Harbor Boulevard, Suite 110, Costa Mesa, CA 92626, USA.

出版信息

Chemosphere. 2015 Oct;137:192-7. doi: 10.1016/j.chemosphere.2015.07.042. Epub 2015 Jul 31.

Abstract

The elevated occurrence of hydrophobic organic chemicals (HOCs) such as polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCBs) and legacy organchlorine pesticides (e.g. chlordane and DDT) in estuarine sediments continues to poses challenges for maintaining the health of aquatic ecosystems. Current efforts to develop and apply protective, science-based sediment quality regulations for impaired waterbodies are hampered by non-concordance between model predictions and measured bioaccumulation and toxicity. A passive sampler incorporating commercially available solid phase microextraction (SPME) fibers was employed in lab and field studies to measure the freely dissolved concentration of target HOCs (Cfree) and determine its suitability as a proxy for bioaccumulation. SPME deduced Cfree for organochlorines was highly correlated with tissue concentrations (Cb) of Macoma and Nereis spp. co-exposed in laboratory microcosms containing both spiked and naturally contaminated sediments. This positive association was also observed in situ for endemic bivalves, where SPME samplers were deployed for up to 1 month at an estuarine field site. The concordance between Cb and Cfree for PAH was more variable, in part due to likely biotransformation by model invertebrates. These results indicate that SPME passive samplers can serve as a proxy for bioaccumulation of sediment-associated organochlorines in both lab and field studies, reducing the uncertainty associated with model predictions that do not adequately account for differential bioavailability.

摘要

疏水性有机化学品(HOCs)如多环芳烃(PAH)、多氯联苯(PCBs)和传统有机氯农药(如氯丹和滴滴涕)在河口沉积物中的高发生率继续对维持水生生态系统的健康构成挑战。目前,为受损害的水体制定和应用具有保护作用的、基于科学的沉积物质量法规的努力受到模型预测与实测生物累积和毒性之间的不一致性的阻碍。一种包含市售固相微萃取(SPME)纤维的被动采样器在实验室和野外研究中被用来测量目标 HOCs 的自由溶解浓度(Cfree),并确定其作为生物累积替代物的适用性。SPME 推断的有机氯的 Cfree 与在含有添加和自然污染沉积物的实验室微宇宙中共同暴露的 Macoma 和 Nereis 属的组织浓度(Cb)高度相关。这种正相关关系也在原位观察到了地方特有双壳类动物中,在河口野外站点,SPME 采样器的部署时间长达 1 个月。PAH 的 Cb 和 Cfree 之间的一致性更具可变性,部分原因是模型无脊椎动物可能发生生物转化。这些结果表明,SPME 被动采样器可以作为实验室和野外研究中与沉积物相关的有机氯生物累积的替代物,减少了模型预测中由于没有充分考虑到差异生物利用度而导致的不确定性。

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