Effects of the meteorological variability on regional air quality in East Asia

被引:77
作者
Jeong, Jaein I. [1 ]
Park, Rokjin J. [1 ]
机构
[1] Seoul Natl Univ, Sch Earth & Environm Sci, Seoul 151742, South Korea
关键词
Air pollution; Meteorological variability; Ozone; Secondary inorganic aerosol; Chemical transport model; UNITED-STATES; TROPOSPHERIC OZONE; AEROSOL EMISSIONS; MODEL DESCRIPTION; BOUNDARY-LAYER; CLIMATE-CHANGE; CLOUD COVER; POLLUTION; CHINA; PM2.5;
D O I
10.1016/j.atmosenv.2012.11.061
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We examine the effects of the meteorological variability on 03 and SO42--NO3--NH4+ aerosol concentrations in East Asia using 3-D chemical transport model (GEOS-Chem) simulations for the period of 1985-2006. The model was driven by the GEOS assimilated meteorology with the emission estimates from the Streets et al. inventory with annual scale factors of Regional Emission inventory in Asia (REAS). Over the past two decades precursor emissions have been dramatically increased. Our model simulations however show strong non-linear responses of oxidation products to the increases of those precursors. The analysis of simulated results shows significant effects of meteorological variability on O-3 and SO42--NO3--NH4+ concentrations. Springtime O-3 concentration has been generally increased over the past two decades mainly due to increases in anthropogenic precursors emissions but concurrent changes in meteorology including decreases of cloud covers and increases of temperature further enhance O-3 increases in East Asia. Our analysis reveals that changes in meteorology account for 30% of total O-3 increases in East Asia over the past two decades. On the contrary, increases in mixing depth suppress increases of (NH4)(2)SO4 concentrations in summer but decreases in mixing depth in winter result in enhancement of NH4NO3 aerosols concentrations up to 4 mu g m(-3) in eastern China. Effects of meteorological variability on SO42--NO3--NH4+ aerosol concentrations are thus seasonally dependent such as a decrease in summer by 4% but an increase by 7% in winter over the past two decades. This result indicates that the meteorological conditions have changed more favorable for the PM air quality degradation in winter. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:46 / 55
页数:10
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