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2011 - 2018年北极地区多氯联苯和有机氯农药的大气浓度及时间趋势

Atmospheric concentrations and temporal trends of polychlorinated biphenyls and organochlorine pesticides in the Arctic during 2011-2018.

作者信息

Hao Yanfen, Li Yingming, Wania Frank, Yang Ruiqiang, Wang Pu, Zhang Qinghua, Jiang Guibin

机构信息

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China; University of Chinese Academy of Sciences, Beijing, 100049, China.

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China; University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Chemosphere. 2021 Mar;267:128859. doi: 10.1016/j.chemosphere.2020.128859. Epub 2020 Nov 4.

Abstract

Passive air samples were deployed in Ny-Ålesund and London Island (Svalbard, High Arctic) annually for seven years (2011-2018) to investigate concentrations, temporal trends and potential sources of selected persistent organic pollutants (POPs). Nine polychlorinated biphenyls and twelve organochlorine pesticides were detected in all samples, with 3,3'-dichlorobiphenyl (PCB-11) being the prevalent congener. Concentrations of most compounds were declining. The ratio of the α- and γ-isomer of hexachlorocyclohexane (HCH) in Arctic air was comparable with that in technical HCH mixtures, but higher than that in the atmosphere of other countries, thereby indicating the impact of historical use as well as the possible photoisomerization of the γ- into the α-isomer. The parent dichlorodiphenyltrichloroethane (DDT) was always less abundant than its degradation products dichlorodiphenylethylene (DDE), indicative of the impact of aged DDT sources in the Arctic atmosphere. However, o,p'-/p,p'-DDT ratios suggest only a minor contribution of dicofol-type DDT. A slightly declining temporal trend of the trans-chlordane/cis-chlordane ratio indicated the impact of secondary sources. The atmospheric distribution of the investigated POPs in the Arctic was mainly attributed to long-range atmospheric transport, whereas the influence of human activities from the scientific research stations was minor.

摘要

在7年时间里(2011 - 2018年),每年都在北极斯瓦尔巴群岛的新奥尔松和伦敦岛采集被动空气样本,以调查选定的持久性有机污染物(POPs)的浓度、时间趋势和潜在来源。在所有样本中均检测出9种多氯联苯和12种有机氯农药,其中3,3'-二氯联苯(PCB - 11)是最主要的同系物。大多数化合物的浓度都在下降。北极空气中六氯环己烷(HCH)的α - 异构体和γ - 异构体的比例与工业用HCH混合物中的比例相当,但高于其他国家大气中的比例,这表明了历史使用的影响以及γ - 异构体可能光异构化为α - 异构体的情况。母体二氯二苯基三氯乙烷(DDT)的含量始终低于其降解产物二氯二苯乙烯(DDE),这表明了老化的DDT源对北极大气的影响。然而,o,p'-/p,p'-DDT比例表明三氯杀螨醇型DDT的贡献较小。反式氯丹/顺式氯丹比例呈略微下降的时间趋势,这表明了二次源的影响。北极地区所调查的持久性有机污染物的大气分布主要归因于长距离大气传输,而科研站人类活动的影响较小。

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