Effects of meteorology on diurnal and nocturnal levels of priority polycyclic aromatic hydrocarbons and elemental and organic carbon in PM10 at a source and a receptor area in Mexico City

被引:37
作者
Guzman-Torres, Diana [1 ,2 ]
Eiguren-Fernandez, Arantza [1 ]
Cicero-Fernandez, Pablo [3 ]
Maubert-Franco, Marisela [2 ]
Retama-Hernandez, Armando [4 ]
Ramos Villegas, Rafael [4 ]
Miguel, Antonio H. [1 ]
机构
[1] Univ Calif Los Angeles, So Calif Particle Ctr & Supersite, Inst Environm, Los Angeles, CA 90095 USA
[2] Univ Autonoma Metropolitana A, Dept Ciencias Basicas, Mexico City 22000, DF, Mexico
[3] Univ Calif Los Angeles, Sch Publ Hlth, Dept Environm Hlth Sci, Los Angeles, CA 90095 USA
[4] Secretaria Medio Ambiente Gobierno DF, DGGAA, Mexico City, DF, Mexico
关键词
Polycyclic aromatic hydrocarbons; Elemental carbon; Organic carbon; Meteorology; Mexico City; PM10; PARTICULATE MATTER; AIR-POLLUTION; BLACK CARBON; VAPOR-PHASE; AEROSOL; EXPOSURE; LYMPHOCYTES; POLLUTANTS; CALIFORNIA; EMISSIONS;
D O I
10.1016/j.atmosenv.2009.03.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
PM10 levels of the 16 US-EPA Priority Pollutant polycyclic aromatic hydrocarbons (PAHs) were measured from March 17 to 31, 2003, in 8-h time bins (morning, afternoon and nighttime) at Merced, a source site dominated by vehicular traffic emissions near the center of Mexico City, and at Pedregal, a receptor area located downwind in a residential area of low traffic. Along with PAH, elemental (EC) and organic carbon (OC), mass, and prevailing meteorological parameters were measured. At the source location, measured concentrations of benzo[a]pyrene (BAP), an agent suspected of being carcinogenic to humans and of causing oxidative DNA damage, reached concentrations as high as 2.04 and 2.11 ng m(-3) during the morning of a weekday and the night period of a holiday. Compared with source dominated areas in Central Los Angeles, the BAP levels found in Central Mexico City are approximately 6 times higher. Benzo[ghi]perylene (BGP) levels were, in general, the highest among the target PAH, both at the source (7.2 ng m(-3)) and the receptor site (2.8 ng m(-3)), suggesting that, at both locations, exhaust emission by light-duty (LD) vehicles is an important contributor to the atmospheric PAH burden. Higher PAH concentrations were observed during the morning period (5:00-13:00 h) at the source and the receptor site. The concentrations of PAHs found predominantly in the particle-phase (MW > 202) correlated well (r = 0.57-0.71) with the occurrence of surface thermal inversions and with mixing heights (r = -0.57 to -0.72). Organic and elemental carbon ratios also indicated that Pedregal is impacted by secondary aerosols during the afternoon hours. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2693 / 2699
页数:7
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