Gioia Rosalinda, Sweetman Andy J, Jones Kevin C
Centre for Chemicals Management, Department of Environmental Science, Lancaster Environment Centre, Lancaster University, Lancaster, LA1 4YQ, UK.
Environ Sci Technol. 2007 Apr 1;41(7):2165-71. doi: 10.1021/es0626739.
Passive air samplers (polyurethane foam disks) were deployed at 23 background locations along a broadly west-east transect in 8 northern European countries and analyzed for PCBs, PBDEs, PAHs, and a range of organochlorine pesticides (HCB, DDTs, and DDEs). PCBs and PAHs were highest at the center of the transect (Denmark) and lowest in northern Norway. HCB was relatively uniformly distributed, reflecting its persistence and high degree of mixing in air. Higher DDE and DDT levels occurred in Eastern Europe and at several sites in Central Europe. PBDE levels were generally similar at all sites, but lower for some locations in Eastern Europe and Ireland. Emissions information for PCBs, HCB, and PBDEs was used as input for a multi-media chemical fate model, to generate predicted air concentrations and compare with these measured values. Different scenarios were highlighted by this exercise: (i) country and compound combinations where the national inventory gave predicted air concentrations in close agreement with those measured (e.g., PCBs in the UK); (ii) country and compound combinations where predicted concentrations were well below those measured, but where advection of emissions from elsewhere is likely to be important (e.g., PCBs in Norway); (iii) consistent underestimation of compound concentrations by the emissions modeling (i.e., HCB); and (iv) general overestimation of ambient concentrations (i.e., PBDEs). Air mass trajectory analysis showed the likely role of long-range atmospheric transport (LRAT) on national levels. In general, advection from the south and west of Europe appeared to contribute to ambient POPs levels for countries in the center and northeast of the transect. Guidelines are presented as to how countries that want to assess their POPs source inventories can do so with this relatively cheap initial screening approach.
在北欧8个国家,沿着大致东西走向的断面,在23个背景点部署了被动空气采样器(聚氨酯泡沫盘),并对其进行多氯联苯(PCBs)、多溴二苯醚(PBDEs)、多环芳烃(PAHs)以及一系列有机氯农药(六氯苯(HCB)、滴滴涕(DDTs)和滴滴伊(DDEs))的分析。多氯联苯和多环芳烃在断面中部(丹麦)含量最高,在挪威北部最低。六氯苯分布相对均匀,反映出其在空气中的持久性和高度混合性。东欧和中欧的几个地点滴滴伊和滴滴涕水平较高。多溴二苯醚水平在所有地点总体相似,但东欧和爱尔兰的一些地点较低。多氯联苯、六氯苯和多溴二苯醚的排放信息被用作多媒体化学归宿模型的输入,以生成预测的空气浓度并与这些测量值进行比较。该研究突出了不同的情景:(i)国家清单给出的预测空气浓度与测量值密切一致的国家和化合物组合(例如英国的多氯联苯);(ii)预测浓度远低于测量值,但其他地方的排放平流可能很重要的国家和化合物组合(例如挪威的多氯联苯);(iii)排放模型对化合物浓度的持续低估(即六氯苯);以及(iv)对环境浓度的普遍高估(即多溴二苯醚)。气团轨迹分析表明了长距离大气传输(LRAT)在国家层面上可能发挥的作用。总体而言,来自欧洲南部和西部的平流似乎对断面中部和东北部国家的环境持久性有机污染物水平有贡献。文中给出了关于希望评估其持久性有机污染物源清单的国家如何通过这种相对廉价的初步筛选方法来进行评估的指导方针。