Jaward Foday M, Farrar Nick J, Harner Tom, Sweetman Andrew J, Jones Kevin C
Department of Environmental Science, Institute of Environmental and Natural Sciences, Lancaster University, Lancaster LA1 4YQ, United Kingdom.
Environ Toxicol Chem. 2004 Jun;23(6):1355-64. doi: 10.1897/03-420.
This study presents concurrently sampled ambient air data for a range of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated naphthalenes (PCNs) at the continental scale. This was achieved with a passive air sampling system, by deploying polyurethane foam disks, which were prepared in one laboratory, sealed to prevent contamination, sent out by courier to volunteers participating in different countries, exposed for six weeks, collected, resealed, and returned to the laboratory for analysis. The study area was Europe, a region with a history of extensive persistent organic pollutants usage and emission, and with marked national differences in population density, the degree of urbanization and industrial and agricultural development. Samplers were deployed at remote, rural, and urban locations in 22 countries. Calculated air concentrations were broadly in line with those obtained by conventional active air sampling techniques, for both compound classes and for compounds existing predominantly in the gas and particle phases. The geographical compound distribution reflected suspected regional emission patterns and highlighted localized source areas. Both PAH and PCN levels varied by more than two orders of magnitude. The implications for sources are discussed.
本研究在大陆尺度上同时呈现了一系列多环芳烃(PAHs)和多氯萘(PCNs)的环境空气采样数据。这是通过一个被动空气采样系统实现的,即部署在一个实验室制备的聚氨酯泡沫盘,密封以防止污染,由快递发送给参与不同国家的志愿者,暴露六周,收集后重新密封,然后返回实验室进行分析。研究区域为欧洲,该地区有广泛使用和排放持久性有机污染物的历史,且在人口密度、城市化程度以及工农业发展方面存在显著的国家差异。在22个国家的偏远、农村和城市地区部署了采样器。对于这两类化合物以及主要存在于气相和颗粒相中的化合物,计算得出的空气浓度与通过传统主动空气采样技术获得的浓度大致相符。地理上的化合物分布反映了疑似区域排放模式,并突出了局部源区。PAH和PCN水平的变化均超过两个数量级。文中讨论了其对源的影响。