Troisi Gera M, Bexton Steve, Robinson Ian
School of Engineering and Design, Brunel University, Kingston Lane, Uxbridge, Middlesex, UB8 3PH, UK.
Environ Sci Technol. 2006 Dec 15;40(24):7938-43. doi: 10.1021/es0601787.
Aside from the physical effects of oiling (e.g., hypothermia, dehydration, emaciation), chronic toxicity of polycyclic aromatic hydrocarbons (PAHs) contamination is an important factor influencing long-term recovery of oiled sea birds following an oil spill. Monitoring PAH exposure can help identify populations at risk from toxic effects of PAHs for further study and/or protection. This is the first studyto quantify PAH and metabolite tissue burdens in sea birds directly oiled following oil spills. PAHs and hydroxylated PAHs were quantified in liver samples from oiled Common Guillemots (Uria aalge) stranded along the East Coast of England using gas chromatography-mass spectroscopy (GC-MS). Mean parent and metabolite PAH concentrations were 0.25+/-0.09 (range 0.04-0.97) and 0.52+/-0.14 (range 0.05-1.48) microg/g (wet wt.), respectively. The main source of PAH exposure was via ingestion of crude oil during preening, resulting in PAH uptake and tissue contamination beyond levels expected from exposure via the food chain. PAH composition corresponded with number of benzene rings in each compound and was typical of contamination from petrogenic sources; pentacyclic < tri- and tetracyclic < tricyclic < dicyclic PAHs. The occurrence of PAH metabolites detected in liver samples also provided evidence of the presence and stereoselectivity of hepatic microsomal CYP1A1 in common guillemots.
除了油污的物理影响(如体温过低、脱水、消瘦)外,多环芳烃(PAHs)污染的慢性毒性是影响溢油事故后油污海鸟长期恢复的一个重要因素。监测PAHs暴露有助于识别有PAHs毒性风险的种群,以便进一步研究和/或保护。这是第一项量化溢油事故后直接被油污的海鸟体内PAHs及其代谢物组织负荷的研究。使用气相色谱 - 质谱联用仪(GC - MS)对英格兰东海岸搁浅的油污普通海雀(海鸠)肝脏样本中的PAHs和羟基化PAHs进行了量化。母体和代谢物PAHs的平均浓度分别为0.25±0.09(范围0.04 - 0.97)和0.52±0.14(范围0.05 - 1.48)微克/克(湿重)。PAHs暴露的主要来源是在梳理羽毛时摄入原油,导致PAHs的摄取和组织污染超过了通过食物链暴露预期的水平。PAH的组成与每种化合物中的苯环数量相对应,是典型的石油源污染;五环 < 三环和四环 < 三环 < 二环PAHs。在肝脏样本中检测到的PAH代谢物的存在也证明了普通海雀肝脏微粒体CYP1A1的存在和立体选择性。