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新加坡海洋环境中药物活性和内分泌干扰化合物的出现和分布:水动力和理化性质的影响。

Occurrence and distribution of pharmaceutically active and endocrine disrupting compounds in Singapore's marine environment: influence of hydrodynamics and physical-chemical properties.

机构信息

Singapore-Delft Water Alliance, National University of Singapore, Singapore.

出版信息

Environ Pollut. 2013 Nov;182:1-8. doi: 10.1016/j.envpol.2013.06.028. Epub 2013 Jul 24.

DOI:10.1016/j.envpol.2013.06.028
PMID:23892012
Abstract

The fate and exposure risks of pharmaceutically active compounds (PhACs) and endocrine disrupting chemicals (EDCs) in marine environments are not well-understood. In this study we developed a multi-residue analytical method for quantifying concentrations of forty target compounds in seawater from Singapore. Analyses of samples (n = 24) from eight sites showed the occurrence of several compounds, including gemfibrozil (<0.09-19.8 ng/L), triclosan (<0.55-10.5 ng/L), carbamazepine (<0.28-10.9 ng/L) and ibuprofen (<2.2-9.1 ng/L). A 3D hydrodynamic model for Singapore was used to predict residence time (tR). Principal Components Analysis revealed a strong relationship between tR and contaminant concentrations. While source emissions are undoubtedly important, proximate distance to a wastewater treatment plant had little influence on concentrations. The site with the greatest tR, which exhibited the highest concentrations, is adjacent to Singapore's largest protected wetland reserve. The results highlight an important linkage between hydrodynamic behavior and contaminant exposure risks in complex coastal marine ecosystems.

摘要

海洋环境中药物活性化合物(PhACs)和内分泌干扰化学物质(EDCs)的命运和暴露风险还没有得到很好的理解。在这项研究中,我们开发了一种多残留分析方法,用于定量测定来自新加坡海水中四十种目标化合物的浓度。对来自八个地点的 24 个样本的分析表明,存在几种化合物,包括吉非贝齐(<0.09-19.8ng/L)、三氯生(<0.55-10.5ng/L)、卡马西平(<0.28-10.9ng/L)和布洛芬(<2.2-9.1ng/L)。用于新加坡的三维水动力模型用于预测停留时间(tR)。主成分分析显示停留时间和污染物浓度之间存在很强的关系。尽管源排放无疑很重要,但离污水处理厂的近距离对浓度几乎没有影响。停留时间最长的地点,其浓度最高,毗邻新加坡最大的湿地保护区。研究结果强调了水动力行为与复杂沿海海洋生态系统中污染物暴露风险之间的重要联系。

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