Department of Civil and Environmental Engineering, University of Southern California, Los Angeles, California 90089, USA.
J Expo Sci Environ Epidemiol. 2010 Jul;20(5):457-68. doi: 10.1038/jes.2009.39. Epub 2009 Jul 22.
We examined the effect of proximity to specific mobile, area, and point sources on the residential outdoor concentrations of fine particulate matter PM (PM(2.5)) and several of its particle components. Integrated (48-h) PM(2.5) samples were collected outside non-smoking residences in Elizabeth, NJ, between summer 1999 and spring 2001. Samples were analyzed for PM(2.5) mass, organic and elemental carbon (OC and EC, respectively), trace elements, particle-phase polycyclic aromatic hydrocarbons (p-PAHs), and other important particle species. Information about the proximity of the study homes to potential mobile and area sources of OC, EC, p-PAHs, sulfur (S), and selenium (Se) (including urban interstate highways, local roadways, the Newark International Airport, the Elizabeth seaport, and a nearby refinery in Linden, NJ) were retrieved from a database that included detailed emissions, meteorological, and geographical data for the study area. The dependence of residential outdoor concentrations on source proximity and on various meteorological parameters was then examined for each species by multiple linear regression analysis. As expected, the predicted ambient air concentrations of all particle species (except S, Se) decreased with increasing distance from the sources. Although the enhancement in PM(2.5) and OC levels outside the study homes closest to primary PM sources was modest (e.g., 1.6 and 2.5 times the background levels 37 m from interstate highways), the elevation of EC and p-PAH concentrations was substantial outside the closest study homes (i.e., about 20 times for p-PAHs 37 m from interstate highways and about 14 times for EC 192 m from the refinery in Linden, NJ). The predicted EC concentrations 192 and 500 m from the oil refinery were 22.8 and 3.0 microgC/m(3), compared with an urban background of 1 microgC/m(3). Thus, emissions from this source might dramatically affect EC exposure for residents living in its close proximity.
我们研究了特定移动源、区域源和点源的接近程度对居民户外细颗粒物 PM(PM(2.5))和其几个颗粒成分浓度的影响。1999 年夏到 2001 年春,在新泽西州伊丽莎白市的非吸烟居民户外采集了(48 小时)整合 PM(2.5)样本。这些样本分析了 PM(2.5)质量、有机碳和元素碳(OC 和 EC)、痕量元素、颗粒态多环芳烃(p-PAHs)和其他重要颗粒物质。关于研究家庭与 OC、EC、p-PAHs、硫(S)和硒(Se)(包括城市州际公路、地方道路、纽瓦克国际机场、伊丽莎白海港和新泽西州林登的附近炼油厂)潜在移动源和区域源的接近程度的信息,是从一个数据库中检索到的,该数据库包括研究区域的详细排放、气象和地理数据。然后,通过多元线性回归分析,针对每种物质,考察了户外浓度对源接近程度和各种气象参数的依赖关系。正如预期的那样,除 S、Se 外,所有颗粒物质的预测环境空气浓度都随着与源距离的增加而降低。尽管研究家庭最接近的主要 PM 源的 PM(2.5)和 OC 水平略有增加(例如,距州际公路 37 米处高出背景水平 1.6 和 2.5 倍),但 EC 和 p-PAH 浓度的升高幅度较大(即,距州际公路 37 米处的 p-PAHs 约 20 倍,距新泽西州林登炼油厂 192 米处的 EC 约 14 倍)。距炼油厂 192 和 500 米处的预测 EC 浓度分别为 22.8 和 3.0 μgC/m(3),而城市背景为 1 μgC/m(3)。因此,来自该源的排放可能会极大地影响居住在其附近的居民的 EC 暴露。