首页> 外文期刊>The Science of the Total Environment >Modem and historical fluxes of halogenated organic contaminants to a lake in the Canadian arctic, as determined from annually laminated sediment cores
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Modem and historical fluxes of halogenated organic contaminants to a lake in the Canadian arctic, as determined from annually laminated sediment cores

机译:由每年叠层的沉积物核心确定的卤化有机污染物到加拿大北极湖的现代和历史通量

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Two annually laminated cores collected from Lake DV09 on Devon Island in May 1999 were dated using Pb-210 and Cs-137, and analyzed for a variety of halogenated organic contaminants (HOCs), including polychlorinated biphenyls (PCBs), organochlorine pesticides, short-chain polychlormated n-alkanes (sPCAs), polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), and polybrominated diphenyl ethers (PBDEs). Dry weight HOC concentrations in Lake DV09 sediments were generally similar to other remote Arctic lakes. Maximum HOC fluxes often agreed well with production maxima, although many compound groups exhibited maxima at or near the sediment surface, much later than peak production. The lower than expected HOC concentrations in older sediment slices may be due to anaerobic degradation and possibly to dilution resulting from a temporary increase in sedimentation rate observed between the mid-1960s and 1970s. Indeed, temporal trends were more readily apparent for those compound classes when anaerobic metabolites were also analyzed, such as for DDT and toxaphene. However, it is postulated here for the first time that the maximum or increasing HOC surface fluxes observed for many of the major compound classes in DV09 sediments may be influenced by climate variation and the resulting increase in algal primary productivity which could drive an increasing rate of HOC scavenging from the water column. Both the fraction (F-TC) and enantiomer fraction (EF) of trans-chlordane (TC) decreased significantly between 1957 and 1997, suggesting that recent inputs to the lake are from weathered chlordane sources. PCDD/Fs showed a change in sources from pentachlorophenol (PeCP) in the 1950s and 1960s to combustion sources into the 1990s. Improvements in combustion technology may be responsible for the reducing the proportion of TCDF relative to OCDD in the most recent slice. Crown Copyright © 2005 Published by Elsevier B.V. All rights reserved.
机译:1999年5月从德文岛的DV09湖收集了两个每年叠合的岩心,这些岩心使用Pb-210和Cs-137进行了测年,并分析了各种卤代有机污染物(HOC),包括多氯联苯(PCBs),有机氯农药,链式多氯代正构烷烃(sPCA),多氯代二苯并对二恶英和二苯并呋喃(PCDD / Fs)以及多溴代二苯醚(PBDEs)。 DV09湖沉积物中的干重HOC浓度通常与其他偏远的北极湖相似。尽管许多化合物组在沉积物表面或其附近表现出最大值,但比峰值产量要晚得多,但最大HOC通量通常与产量最大值非常吻合。在较老的沉积物中,HOC浓度低于预期,可能是由于厌氧降解,可能是由于1960年代中期至1970年代中期观测到的沉积速率暂时增加而导致的稀释作用。的确,在分析厌氧代谢产物时,对于那些化合物类别来说,时间趋势也更加明显,例如滴滴涕和毒杀芬。但是,这是首次假定在DV09沉积物中许多主要化合物类别中观察到的最大HOC表面通量可能会受到气候变化的影响,从而导致藻类初级生产力的增加,这可能会导致藻类初级生产力的增加。 HOC从水柱中清除。在1957年至1997年之间,反式氯丹(TC)的馏分(F-TC)和对映异构体分数(EF)均显着下降,这表明该湖的近期输入来自风化的氯丹。 PCDD / Fs从1950年代和1960年代的五氯苯酚(PeCP)到1990年代的燃烧源发生了变化。燃烧技术的改进可能是导致最近切片中TCDF相对OCDD的比例降低的原因。皇冠版权© 2005由Elsevier B.V.出版,保留所有权利。

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