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Gaseous and Freely-Dissolved PCBs in the Lower Great Lakes based on Passive Sampling: Spatial Trends and Air-water Exchange

机译:基于被动采样的大湖下游气态和自由溶解的多氯联苯:空间趋势和空气-水交换

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摘要

Polyethylene passive sampling was performed to quantify gaseous and freely dissolved polychlorinated biphenyls (PCBs) in the air and water of Lakes Erie and Ontario during 2011–2012. In view of differing physical characteristics and the impacts of historical contamination by PCBs within these lakes, spatial variation of PCB concentrations and air–water exchange across these lakes may be expected. Both lakes displayed statistically similar aqueous and atmospheric PCB concentrations. Total aqueous concentrations of 29 PCBs ranged from 1.5 pg L–1 in the open lake of Lake Erie (site E02) in 2011 spring to 105 pg L–1 in Niagara (site On05) in 2012 summer, while total atmospheric concentrations were 7.7–634 pg m–3 across both lakes. A west-to-east gradient was observed for aqueous PCBs in Lake Erie. River discharge and localized influences (e.g., sediment resuspension and regional alongshore transport) likely dominated spatial trends of aqueous PCBs in both lakes. Air–water exchange fluxes of Σ7PCBs ranged from −2.4 (±1.9) ng m–2 day–1 (deposition) in Sheffield (site E03) to 9.0 (±3.1) ng m–2 day–1 (volatilization) in Niagara (site On05). Net volatilization of PCBs was the primary trend across most sites and periods. Almost half of variation in air–water exchange fluxes was attributed to the difference in aqueous concentrations of PCBs. Uncertainty analysis in fugacity ratios and mass fluxes in air–water exchange of PCBs indicated that PCBs have reached or approached equilibrium only at the eastern Lake Erie and along the Canadian shore of Lake Ontario sites, where air–water exchange fluxes dominated atmospheric concentrations.
机译:进行了聚乙烯无源采样,以量化2011–2012年伊利湖和安大略湖的空气和水中的气态和自由溶解的多氯联苯(PCB)。鉴于这些湖泊内不同的物理特征和历史污染对多氯联苯的影响,可以预期这些湖泊中多氯联苯浓度的空间变化和空气-水交换。两个湖泊的水和大气PCB浓度在统计上均相似。 29种多氯联苯的总水溶液浓度从2011年春季的伊利湖开阔湖(E02站点)的1.5 pg L–1到2012年夏季的尼亚加拉(On05站点)的105 pg L–1,而大气中的总浓度为7.7–1。横跨两个湖泊的634 pg m–3。在伊利湖中,含水多氯联苯观察到了从西向东的梯度。河流排放和局部影响(例如泥沙再悬浮和区域沿海运输)可能主导了两个湖泊中含水多氯联苯的空间趋势。 Σ7PCBs的空气-水交换通量的范围从谢菲尔德(站点E03)的-2.4(±1.9)ng m–2天-1(沉积)到尼亚加拉的9.0(±3.1)ng m–2天-1(挥发)(网站On05)。多氯联苯的净挥发是大多数地点和时期的主要趋势。空气-水交换通量变化的几乎一半归因于多氯联苯中水含量的差异。多氯联苯的空气-水交换中的逸度比和质量通量的不确定性分析表明,多氯联苯仅在伊利湖东部和加拿大安大略湖沿岸的地点达到或接近平衡,那里空气-水交换通量主导着大气浓度。

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