Motelay-Massei Anne, Harner Tom, Shoeib Mahiba, Diamond Miriam, Stern Gary, Rosenberg Bruno
Meteorological Service of Canada, Environment Canada, 4905 Dufferin Street, Toronto, Ontario, Canada M3H 5T4.
Environ Sci Technol. 2005 Aug 1;39(15):5763-73. doi: 10.1021/es0504183.
This is the second of two papers demonstrating the feasibility of using passive air samplers to investigate persistent organic pollutants along an urban-rural transect in Toronto. The first paper investigated spatial trends for polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs). This second paper investigates the seasonality of air concentrations for polycyclic aromatic hydrocarbons (PAHs), PCBs, and OCPs along this transect. Air samplers, consisting of polyurethane foam (PUF) disks housed in stainless steel domed chambers, were deployed for three 4-month integration periods from June 2000 to July 2001. The seasonal variations of derived air concentrations for PAHs, PCBs, and OCPs reflected the different source characteristics for these compounds. PAHs showed a strong urban-rural gradient with maximum concentrations at urban sites during the summer period (July-October). These high summer values in Toronto were attributed to increases in evaporative emissions from petroleum products such as asphalt. PCBs also exhibited a strong urban-rural gradient with maximum air concentrations (approximately 2-3 times higher) during the spring period (April-June). This was attributed to increased surface-air exchange of PCBs that had accumulated in the surface layer over the winter. alpha-HCH was fairly uniformly distributed, spatially and temporally, as expected. This pattern and the derived air concentration of approximately 35 to approximately 100 pg m(-3) agreed well with high volume air data from this region, adding confidence to the operation of the passive samplers and showing that site-to-site differences in sampling rates was not an issue. For other OCPs, highest concentrations were observed during the spring period. This was associated with either (i) their local and/or regional application (gamma-HCH, endosulfan) and (ii) their revolatilization (chlordanes, DDT isomers, dieldrin, and toxaphene). Principal component analysis resulted in clusters for the different target chemicals according to their chemical class/source type. The results of this study demonstrate how such a simple sampling technique can provide both spatial and seasonal information. These data, integrated over seasons, can be used to evaluate contaminant trends and the potential role of large urban centers as sources of some semivolatile compounds to the regional environment, including the Great Lakes ecosystem.
本文是两篇论文中的第二篇,论证了使用被动空气采样器沿多伦多城乡断面调查持久性有机污染物的可行性。第一篇论文研究了多氯联苯(PCBs)和有机氯农药(OCPs)的空间趋势。第二篇论文研究了沿该断面多环芳烃(PAHs)、多氯联苯和有机氯农药空气浓度的季节性变化。空气采样器由置于不锈钢圆顶室中的聚氨酯泡沫(PUF)盘组成,于2000年6月至2001年7月进行了三个为期4个月的积分期部署。多环芳烃、多氯联苯和有机氯农药衍生空气浓度的季节变化反映了这些化合物不同的源特征。多环芳烃呈现出强烈的城乡梯度,夏季(7月至10月)城市站点浓度最高。多伦多夏季的这些高值归因于石油产品(如沥青)蒸发排放的增加。多氯联苯也呈现出强烈的城乡梯度,春季(4月至6月)空气浓度最高(约高2至3倍)。这归因于冬季积累在表层的多氯联苯的地表 - 空气交换增加。正如预期的那样,α - 六氯环己烷在空间和时间上分布相当均匀。这种模式以及约35至约100 pg m(-3)的衍生空气浓度与该地区的高容量空气数据吻合良好,增加了对被动采样器运行的信心,并表明采样率的站点间差异不是问题。对于其他有机氯农药,春季观察到最高浓度。这与(i)它们的本地和/或区域应用(γ - 六氯环己烷、硫丹)以及(ii)它们的再挥发(氯丹、滴滴涕异构体、狄氏剂和毒杀芬)有关。主成分分析根据不同目标化学品的化学类别/源类型得出聚类结果。本研究结果表明,这样一种简单的采样技术如何能够提供空间和季节信息。这些按季节整合的数据可用于评估污染物趋势以及大型城市中心作为某些半挥发性化合物向区域环境(包括五大湖生态系统)的源的潜在作用。