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Concentrations and sources of polycyclic aromatic hydrocarbons in surface coastal sediments of the northern Gulf of Mexico

机译:墨西哥湾北部沿海近岸沉积物中多环芳烃的浓度和来源

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Coastal sediments in the northern Gulf of Mexico have a high potential of being contaminated by petroleum hydrocarbons, such as polycyclic aromatic hydrocarbons (PAHs), due to extensive petroleum exploration and transportation activities. In this study we evaluated the spatial distribution and contamination sources of PAHs, as well as the bioavailable fraction in the bulk PAH pool, in surface marsh and shelf sediments (top 5 cm) of the northern Gulf of Mexico. PAH concentrations in this region ranged from 100 to 856 ng g−1, with the highest concentrations in Mississippi River mouth sediments followed by marsh sediments and then the lowest concentrations in shelf sediments. The PAH concentrations correlated positively with atomic C/N ratios of sedimentary organic matter (OM), suggesting that terrestrial OM preferentially sorbs PAHs relative to marine OM. PAHs with 2 rings were more abundant than those with 5–6 rings in continental shelf sediments, while the opposite was found in marsh sediments. This distribution pattern suggests different contamination sources between shelf and marsh sediments. Based on diagnostic ratios of PAH isomers and principal component analysis, shelf sediment PAHs were petrogenic and those from marsh sediments were pyrogenic. The proportions of bioavailable PAHs in total PAHs were low, ranging from 0.02% to 0.06%, with higher fractions found in marsh than shelf sediments. PAH distribution and composition differences between marsh and shelf sediments were influenced by grain size, contamination sources, and the types of organic matter associated with PAHs. Concentrations of PAHs in the study area were below effects low-range, suggesting a low risk to organisms and limited transfer of PAHs into food web. From the source analysis, PAHs in shelf sediments mainly originated from direct petroleum contamination, while those in marsh sediments were from combustion of fossil fuels.
机译:由于广泛的石油勘探和运输活动,墨西哥湾北部的沿海沉积物极有可能被石油烃(例如多环芳烃)污染。在这项研究中,我们评估了墨西哥湾北部墨西哥湾的表层沼泽和陆架沉积物(顶部5厘米)中多环芳烃的空间分布和污染源以及大量多环芳烃池中的生物利用度。该区域的PAH浓度范围为100至856 ng g-1,密西西比河口沉积物中的PAH浓度最高,其次是沼泽沉积物,而陆架沉积物中的浓度最低。 PAH浓度与沉积有机物(OM)的原子C / N比呈正相关,表明相对于海洋OM,陆地OM优先吸附PAH。在大陆架沉积物中,具有2个环的多环芳烃比具有5–6个环的多环芳烃更丰富,而在沼泽沉积物中则相反。这种分布模式表明架子和沼泽沉积物之间的污染源不同。根据多环芳烃异构体的诊断率和主成分分析,架子沉积物多环芳烃是岩石成因的,而沼泽沉积物中的多环芳烃是致热的。可生物利用的多环芳烃在总多环芳烃中的比例很低,在0.02%至0.06%之间,在沼泽中发现的比例要比陆架沉积物高。沼泽,陆架沉积物之间的多环芳烃分布和成分差异受粒度,污染源以及与多环芳烃有关的有机物类型的影响。研究区域中PAHs的浓度低于低影响范围,表明对生物体的风险较低,并且PAHs向食物网的转移有限。从来源分析来看,陆架沉积物中的PAHs主要来自直接的石油污染,而沼泽沉积物中的PAHs来自化石燃料的燃烧。

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