Brun Guy L, Vaidya Om C, Léger Martin G
Environmental Conservation Branch, Environment Canada, P.O. Box 23005, Moncton, NB, E1A 6S8, Canada.
Environ Sci Technol. 2004 Apr 1;38(7):1941-8. doi: 10.1021/es034645l.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental contaminants. The semivolatile organic compounds may disperse into the atmosphere by direct input from several sources such as the burning of fossil fuels, from motor vehicle emissions, and forest fires. Once in the atmosphere, they may travel great distances before being deposited to the earth's surface by the scavenging action of rain and snow. Up to 14 PAHs were determined in wet precipitation samples collected monthly from five sites in the four Canadian Atlantic Provinces during 1980-2001. The relatively more volatile PAHs (phenanthrene, fluoranthene, naphthalene, and pyrene) were predominant in the samples. Significant (P < 0.05) spatial variations in the deposition of some PAHs were observed among sites, but there were no consistent geographic patterns. Seasonal patterns were discernible with peak deposition for sigma6&14 PAHs occurring during the colder months of the year (December to March) and coinciding with higher energy consumption for heating and transport. The monthly volume weighed mean concentration for sigma6 PAHs has declined steadily since the mid-1980s at Kejimkujik National Park in southwest Nova Scotia, with a calculated half-life of 6.4 +/- 0.3 years. The maximum annual deposition flux of 20 microg m(-2) yr(-1) reached in 1985 for sigma6 PAHs decreased approximately 1 order of magnitude by the year 2000. The decrease in sigma6&14 PAHs for the region was found to be correlated (P < 0.05) with decreasing sulfate ion concentrations in the precipitation. The implementation of air pollution abatement programs in Canada, the United States, and elsewhere, switching to cleaner sources of energy and improved technology during the pastfew decades is most likely responsible for the observed decline.
多环芳烃(PAHs)是普遍存在的环境污染物。这些半挥发性有机化合物可通过多种来源直接排放进入大气,如化石燃料燃烧、机动车尾气排放和森林火灾。一旦进入大气,它们可能会远距离传输,然后通过雨雪的清除作用沉降到地球表面。在1980 - 2001年期间,每月从加拿大四个大西洋省份的五个地点采集的湿沉降样品中测定了多达14种多环芳烃。样品中相对挥发性较强的多环芳烃(菲、荧蒽、萘和芘)占主导地位。在各采样点之间观察到某些多环芳烃沉降存在显著(P < 0.05)的空间差异,但没有一致的地理模式。季节模式明显,Σ6&14多环芳烃的沉降峰值出现在一年中较冷的月份(12月至3月),且与取暖和运输的能源消耗增加相吻合。自20世纪80年代中期以来,新斯科舍省西南部的凯吉姆库吉克国家公园Σ6多环芳烃的月体积加权平均浓度稳步下降,计算得出的半衰期为6.4±0.3年。1985年Σ6多环芳烃的最大年沉降通量达到20μg m(-2) yr(-1),到2000年下降了约1个数量级。该地区Σ6&14多环芳烃的减少被发现与降水中硫酸根离子浓度的降低相关(P < 0.05)。在过去几十年里,加拿大、美国和其他地方实施的空气污染减排计划,转向更清洁的能源来源和改进技术,很可能是观察到的下降趋势的原因。