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Sources and environmental fate of pyrogenic polycyclic aromatic hydrocarbons (PAHs) in the Arctic

机译:北极热源性多环芳烃的来源和环境命运

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Polycyclic aromatic hydrocarbons (PAHs) are large class of hydrophobic, semi-volatile organic contaminants that may enter the environment from both natural sources and anthropogenic activities. Pyrogenic PAHs arise from the incomplete combustion of fossil fuels and organic matter and following dispersal via long-range transport and may subsequently deposit in surface waters, soils and sediments of remote regions, including the Arctic. The current review summarizes and discusses Arctic data that is available for combustion-derived PAHs between 2004 and early 2018, focusing largely on data collected from remote, unexploited Arctic regions and from studies that provide some evidence of a pyrogenic origin. The increasing use of attribution ratios, which aid in discriminating PAHs from petrogenic or pyrogenic sources, suggest PAHs found in Arctic marine waters and sediment predominantly originate from natural underwater seeps, while those measured in air, freshwater, and terrestrial environments are likely to have originated from atmospheric and combustion-derived sources. Modeling efforts indicate that atmospheric PAHs in the Canadian and Norwegian Arctic are likely to have originated in the northern hemisphere – predominantly from Western Russia, northern Europe, and North America. East Asia appears to be a minor source of PAHs to the Arctic, despite contributing more than 50% of global PAH emissions. In comparison to the growing data for atmospheric PAHs, environmental data for these compounds in terrestrial and freshwater environments remain scarce. PAHs have been detected in Arctic biota from terrestrial, freshwater and marine environments, indicating exposure, however, levels are generally low, as most organisms efficiently metabolize parent PAHs. Globally, PAH emissions are expected to decline in the future, however models suggest the Arctic may not experience the same magnitude of decline projected for other world regions. Furthermore, future changes in climate may contribute to a re-volatilization of environmental PAHs, providing a source of secondary emissions to the Arctic atmosphere, emphasizing the importance of future monitoring for understanding the sources, fate and impacts of PAHs in the Arctic.
机译:多环芳烃(PAH)是一类疏水性,半挥发性的有机污染物,可能会从自然资源和人为活动进入环境。热解多环芳烃的产生是由于化石燃料和有机物的不完全燃烧,以及通过远程运输扩散之后产生的,随后可能沉积在包括北极在内的偏远地区的地表水,土壤和沉积物中。本篇综述总结并讨论了2004年至2018年初之间可用于燃烧衍生PAHs的北极数据,主要侧重于从偏远未开发的北极地区收集的数据以及提供热原起源证据的研究。归因比的使用不断增加,有助于将PAHs区别于成岩源或热源源,这表明在北极海洋水域和沉积物中发现的PAHs主要源自天然水下渗漏,而在空气,淡水和陆地环境中测量的PAHs可能源自来自大气和燃烧来源。建模工作表明,加拿大和挪威北极地区的大气PAH可能起源于北半球-主要来自俄罗斯西部,北欧和北美。尽管贡献了全球PAH排放量的50%以上,但东亚似乎是北极PAH的次要来源。与大气中多环芳烃的增长数据相比,陆地和淡水环境中这些化合物的环境数据仍然匮乏。在北极生物群中,从陆地,淡水和海洋环境中检测到了PAHs,这表明其暴露水平,但是由于大多数生物都能有效地代谢其母体PAHs,因此其水平普遍较低。在全球范围内,PAH排放有望在未来减少,但是模型表明,北极地区可能不会像其他世界地区那样经历相同程度的减少。此外,未来的气候变化可能会导致环境多环芳烃的重新挥发,为北极大气提供二次排放源,强调未来监测对于了解北极多环芳烃的来源,命运和影响的重要性。

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