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加拿大北极地区的污染物:五年间在了解其来源、存在情况及传播途径方面取得的进展

Contaminants in the Canadian Arctic: 5 years of progress in understanding sources, occurrence and pathways.

作者信息

Macdonal R W, Barrie L A, Bidleman T F, Diamond M L, Gregor D J, Semkin R G, Strachan W M, Li Y F, Wania F, Alaee M, Alexeeva L B, Backus S M, Bailey R, Bewers J M, Gobeil C, Halsall C J, Harner T, Hoff J T, Jantunen L M, Lockhart W L, Mackay D, Muir D C, Pudykiewicz J, Reimer K J, Smith J N, Stern G A

机构信息

Institute of Ocean Sciences, Department of Fisheries and Oceans, Sidney, BC, Canada.

出版信息

Sci Total Environ. 2000 Jun 1;254(2-3):93-234. doi: 10.1016/s0048-9697(00)00434-4.

Abstract

Recent studies of contaminants under the Canadian Northern Contaminants Program (NCP) have substantially enhanced our understanding of the pathways by which contaminants enter Canada's Arctic and move through terrestrial and marine ecosystems there. Building on a previous review (Barrie et al., Arctic contaminants: sources, occurrence and pathways. Sci Total Environ 1992:1-74), we highlight new knowledge developed under the NCP on the sources, occurrence and pathways of contaminants (organochlorines, Hg, Pb and Cd, PAHs, artificial radionuclides). Starting from the global scale, we examine emission histories and sources for selected contaminants focussing especially on the organochlorines. Physical and chemical properties, transport processes in the environment (e.g. winds, currents, partitioning), and models are then used to identify, understand and illustrate the connection between the contaminant sources in industrial and agricultural regions to the south and the eventual arrival of contaminants in remote regions of the Arctic. Within the Arctic, we examine how contaminants impinge on marine and terrestrial pathways and how they are subsequently either removed to sinks or remain where they can enter the biosphere. As a way to focus this synthesis on key concerns of northern residents, a number of special topics are examined including: a mass balance for HCH and toxaphene (CHBs) in the Arctic Ocean; a comparison of PCB sources within Canada's Arctic (Dew Line Sites) with PCBs imported through long-range transport; an evaluation of concerns posed by three priority metals--Hg, Pb and Cd; an evaluation of the risks from artificial radionuclides in the ocean; a review of what is known about new-generation pesticides that are replacing the organochlorines; and a comparison of natural vs. anthropogenic sources of PAH in the Arctic. The research and syntheses provide compelling evidence for close connectivity between the global emission of contaminants from industrial and agricultural activities and the Arctic. For semi-volatile compounds that partition strongly into cold water (e.g. HCH) we have seen an inevitable loading of Arctic aquatic reservoirs. Drastic HCH emission reductions have been rapidly followed by reduced atmospheric burdens with the result that the major reservoir and transport agent has become the ocean. In the Arctic, it will take decades for the upper ocean to clear itself of HCH. For compounds that partition strongly onto particles, and for which the soil reservoir is most important (e.g. PCBs), we have seen a delay in their arrival in the Arctic and some fractionation toward more volatile compounds (e.g. lower-chlorinated PCBs). Despite banning the production of PCB in the 1970s, and despite decreases of PCBs in environmental compartments in temperate regions, the Arctic presently shows little evidence of reduced PCB loadings. We anticipate a delay in PCB reductions in the Arctic and environmental lifetimes measured in decades. Although artificial radionuclides have caused great concern due to their direct disposal on Russian Shelves, they are found to pose little threat to Canadian waters and, indeed, much of the radionuclide inventory can be explained as remnant global fallout, which was sharply curtailed in the 1960s, and waste emissions released under license by the European reprocessing plants. Although Cd poses a human dietary concern both for terrestrial and marine mammals, we find little evidence that Cd in marine systems has been impacted by human activities. There is evidence of contaminant Pb in the Arctic, but loadings appear presently to be decreasing due to source controls (e.g. removal of Pb from gasoline) in Europe and North America. Of the metals, Hg provokes the greatest concern; loadings appear to be increasing in the Arctic due to global human activities, but such loadings are not evenly distributed nor are the pathways by which they enter and move within the Arctic well understood.

摘要

加拿大北方污染物计划(NCP)近期针对污染物开展的研究极大地增进了我们对污染物进入加拿大北极地区并在当地陆地和海洋生态系统中迁移路径的理解。基于之前的一篇综述(巴里等人,《北极污染物:来源、存在情况及路径》。《科学的总环境》1992年:1 - 74),我们着重介绍了NCP在污染物(有机氯、汞、铅、镉、多环芳烃、人工放射性核素)来源、存在情况及路径方面取得的新知识。从全球范围出发,我们研究了选定污染物的排放历史和来源,尤其聚焦于有机氯。随后利用物理和化学性质、环境中的传输过程(如风力、洋流、分配作用)以及模型来识别、理解并阐释工业和农业发达的南部地区的污染物来源与北极偏远地区最终出现污染物之间的联系。在北极地区内部,我们考察了污染物如何影响海洋和陆地路径,以及它们随后是如何被清除到汇区或者仍然留在能够进入生物圈的地方。为了使这一综述聚焦于北方居民的关键关切点,我们探讨了若干专题,包括:北冰洋中六氯环己烷和毒杀芬(CHBs)的质量平衡;加拿大北极地区(德维线站点)的多氯联苯来源与通过长距离传输输入的多氯联苯的比较;对三种优先金属——汞、铅和镉所引发问题的评估;对海洋中人工放射性核素风险的评估;对替代有机氯的新一代农药的已知情况的综述;以及北极地区多环芳烃自然源与人为源的比较。这些研究和综述提供了有力证据,证明工业和农业活动产生的全球污染物排放与北极地区之间存在紧密联系。对于强烈分配到冷水中的半挥发性化合物(如六氯环己烷),我们发现北极水体不可避免地受到了污染。六氯环己烷排放量急剧减少之后,大气负担迅速减轻,结果是主要的储存库和传输介质变成了海洋。在北极地区,上层海洋清除六氯环己烷需要数十年时间。对于强烈分配到颗粒物上且土壤储存库最为重要的化合物(如多氯联苯),我们发现它们到达北极地区有所延迟,并且出现了向挥发性更强的化合物(如低氯代多氯联苯)的某种分馏现象。尽管在20世纪70年代禁止了多氯联苯的生产,并且温带地区环境介质中的多氯联苯含量有所下降,但目前北极地区几乎没有多氯联苯负荷降低的迹象。我们预计北极地区多氯联苯含量的降低会出现延迟,其在环境中的存留时间将以数十年计。尽管人工放射性核素因其被直接倾倒在俄罗斯大陆架上而引发了极大关注,但它们对加拿大海域几乎不构成威胁,实际上,大部分放射性核素存量可解释为20世纪60年代急剧减少的全球沉降残余物以及欧洲后处理厂根据许可排放的废物。尽管镉对陆地和海洋哺乳动物的人类饮食构成了担忧,但我们几乎没有发现海洋系统中的镉受到人类活动影响的证据。北极地区存在污染物铅的证据,但由于欧洲和北美的源头控制措施(如从汽油中去除铅),目前其负荷似乎正在下降。在这些金属中,汞引发的担忧最大;由于全球人类活动,北极地区汞的负荷似乎在增加,但这种负荷分布并不均匀,其进入北极并在北极内部迁移的路径也尚未得到充分理解。

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