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Composition, sources, and potential toxicological significance of PAHs in the surface sediments of the Meiliang Bay, Taihu Lake, China

机译:太湖梅梁湾表层沉积物中多环芳烃的组成,来源及潜在的毒理学意义

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Twenty-five surface sediment samples were collected from Meiliang Bay, Taihu Lake, China, in 2003. The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs), identified as priority pollutants by the USEPA, were determined by gas chromatography equipped with a mass spectrometry detector (GC-MS). Total concentrations of the PAHs ranged from 1207 to 4754 ng/g dry weight. Sediment samples with the highest PAH concentrations were from the northern site of the bay, which is in proximity to the incoming PAH source; the PAH levels in the southern part were relatively low. The observed PAH levels were higher than those in river sediments in China but were lower than those found in sediments of urban areas and harbors. According to the observed molecular indices, PAHs originated largely from the high-temperature pyrolytic process, whereas the petrogenic process was more commonly responsible for PAH contamination in harbors. A good correlation existed between the benzo[a]pyrene level and the total PAH concentration (r=0.97), making benzo[a]pyrene a potential molecular marker for PAH pollution. According to the numerical effect-based sediment quality guideline (SQGs) of the United States, the levels of PAHs at most studied sites in Meiliang Bay, except some sites in the northern part of the bay, should not exert adverse biological effects. In the northern part of the bay, the PAH levels at sites 21 and 22 exceed the effects range low (ERL) and could thus cause acute biological impairments, in comparison with the sediment quality guidelines. The total PAH levels were expressed as the B[a]P toxicity equivalents (TEQs~(carc)) and compared to the contaminated sediments from Guba Pechenga, Barents Sea, Russia.
机译:2003年,从中国太湖梅梁湾采集了25个表面沉积物样品。通过配备质谱检测器的气相色谱法测定了USEPA确定为优先污染物的16种多环芳烃(PAHs)的浓度。 (GC-MS)。 PAHs的总浓度为1207至4754 ng / g干重。 PAH浓度最高的沉积物样品来自海湾的北部站点,该区域靠近传入的PAH源。南部的PAH水平相对较低。观测到的PAH水平高于中国河流沉积物中的PAH水平,但低于市区和港口沉积物中的PAH水平。根据观察到的分子指数,PAHs很大程度上源自高温热解过程,而成岩过程更普遍是港口中PAH污染的原因。苯并[a] py水平与总PAH浓度之间存在良好的相关性(r = 0.97),从而使苯并[a] py成为潜在的PAH污染分子标志。根据美国基于数值效应的沉积物质量准则(SQG),除海湾北部的某些场所外,在美良湾大多数研究地点的PAHs水平不应产生不利的生物学影响。与沉积物质量指南相比,在海湾北部,第21和22位的多环芳烃水平超出了低影响范围(ERL),因此可能导致严重的生物学损伤。 PAH的总含量表示为B [a] P毒性当量(TEQs〜(carc)),并与来自俄罗斯巴伦支海古巴佩城加的被污染沉积物进行了比较。

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