The influence of temperature and aerosol acidity on biogenic secondary organic aerosol tracers: Observations at a rural site in the central Pearl River Delta region, South China

被引:125
作者
Ding, Xiang [1 ,2 ]
Wang, Xin-Ming [1 ]
Zheng, Mei [3 ]
机构
[1] Chinese Acad Sci, Guangzhou Inst Geochem, State Key Lab Organ Geochem, Guangzhou 510640, Guangdong, Peoples R China
[2] Chinese Acad Sci, Pearl River Delta Res Ctr Environm Pollut Control, Guangzhou 510640, Guangdong, Peoples R China
[3] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
SOA; Tracers; Temperature; Aerosol acidity; Pearl River Delta (PRD); SOUTHEASTERN UNITED-STATES; CARBONACEOUS AEROSOL; ATMOSPHERIC AEROSOL; COMPOUND EMISSIONS; URBAN GUANGZHOU; PM2.5; AEROSOLS; ALPHA-PINENE; HONG-KONG; ISOPRENE; POLLUTION;
D O I
10.1016/j.atmosenv.2010.11.057
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
At a rural site in the central Pearl River Delta (PRD) region in south China, fine particle (PM2.5) samples were collected during fall-winter 2007 to measure biogenic secondary organic aerosol (SOA) tracers, including isoprene SOA tracers (3-methyl-2,3,4-trihydroxy-1-butene, 2-methylglyceric acid, 2-methylthreitol and 2-methylerythritol), alpha-pinene SOA tracers (cis-pinonic acid, pinic acid, 3-methyl-1,2,3-butanetricarboxylic acid, 3-hydroxyglutaric acid and 3-hydroxy-4,4-dimethylglutaric acid) and a sesquiterpene SOA tracer (beta-caryophyllinic acid). The isoprene-, alpha-pinene- and sesquiterpene-SOA tracers averaged 30.8 +/- 15.9, 6.61 +/- 4.39, and 0.54 +/- 0.56 ng m(-3), respectively; and 2-methyltetrols (sum of 2-methylthreitol and 2-methylerythritol, 27.6 +/- 15.1 ng m(-3)) and cis-pinonic acid (3.60 +/- 3.76 ng m(-3)) were the dominant isoprene- and alpha-pinene-SOA tracers, respectively. 2-Methyltetrols exhibited significantly positive correlations (p < 0.05) with ambient temperature, probably resulting from the enhanced isoprene emission strength and tracer formation rate under higher temperature. The significantly positive correlation (p < 0.05) between 2-methyltetrols and the estimated aerosol acidity with a slope of 59.4 +/- 13.4 ng m(-3) per mu mol [H+] m(-3) reflected the enhancement of isoprene SOA formation by aerosol acidity, and acid-catalyzed heterogeneous reaction was probably the major formation pathway for 2-methyltetrols in the PRD region. 2-Methylglyceric acid showed poor correlations with both temperature and aerosol acidity. The alpha-pinene SOA tracers showed poor correlations with temperature, probably due to the counteraction between temperature effects on the precursor emission/tracer formation and gas/particle partitioning. Among the alpha-pinene SOA tracers, only cis-pinonic acid and pinic acid exhibited significant correlations with aerosol acidity with slopes of -11.7 +/- 3.7 and -2.2 +/- 0.8 ng m(-3) per mu mol [H+] m(-3), respectively. The negative correlations observed for alpha-pinene SOA tracers might result from their transfer from particle to gas phase with the increase of aerosol acidity. The ratio of cis-pinonic acid plus pinic acid to 3-methyl-1,2,3-butanetricarboxylic acid (MBTCA) ranged from 0.28 to 28.9 with a mean of 7.19, indicating the relatively fresh alpha-pinene SOA tracers during our campaign. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1303 / 1311
页数:9
相关论文
共 54 条
[1]   Optical properties and chemical composition of the atmospheric aerosol in urban Guangzhou, China [J].
Andreae, Meinrat O. ;
Schmid, Otmar ;
Yang, Hong ;
Chand, Duli ;
Yu, Jian Zhen ;
Zeng, Li-Min ;
Zhang, Yuan-Hang .
ATMOSPHERIC ENVIRONMENT, 2008, 42 (25) :6335-6350
[2]  
[Anonymous], NIOSH MAN AN METH
[3]   Spatial and seasonal variations of atmospheric organic carbon and elemental carbon in Pearl River Delta Region, China [J].
Cao, JJ ;
Lee, SC ;
Ho, KF ;
Zou, SC ;
Fung, K ;
Li, Y ;
Watson, JG ;
Chow, JC .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (27) :4447-4456
[4]   Characteristics of carbonaceous aerosol in Pearl River Delta Region, China during 2001 winter period [J].
Cao, JJ ;
Lee, SC ;
Ho, KF ;
Zhang, XY ;
Zou, SC ;
Fung, K ;
Chow, JC ;
Watson, JG .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (11) :1451-1460
[5]   To What Extent Can Biogenic SOA be Controlled? [J].
Carlton, Annmarie G. ;
Pinder, Robert W. ;
Bhave, Prakash V. ;
Pouliot, George A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (09) :3376-3380
[6]   Air pollution in mega cities in China [J].
Chan, Chak K. ;
Yao, Xiaohong .
ATMOSPHERIC ENVIRONMENT, 2008, 42 (01) :1-42
[7]   Formation of secondary organic aerosols through photooxidation of isoprene [J].
Claeys, M ;
Graham, B ;
Vas, G ;
Wang, W ;
Vermeylen, R ;
Pashynska, V ;
Cafmeyer, J ;
Guyon, P ;
Andreae, MO ;
Artaxo, P ;
Maenhaut, W .
SCIENCE, 2004, 303 (5661) :1173-1176
[8]   Hydroxydicarboxylic acids:: Markers for secondary organic aerosol from the photooxidation of α-pinene [J].
Claeys, Magda ;
Szmigielski, Rafal ;
Kourtchev, Ivan ;
Van der Veken, Pieter ;
Vermeylen, Reinhilde ;
Maenhaut, Willy ;
Jaoui, Mohammed ;
Kleindienst, Tadeusz E. ;
Lewandowski, Michael ;
Offenberg, John H. ;
Edney, Edward O. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (05) :1628-1634
[9]   Spatial and seasonal trends in biogenic secondary organic aerosol tracers and water-soluble organic carbon in the southeastern United States [J].
Ding, Xiang ;
Zheng, Mei ;
Yu, Liping ;
Zhang, Xiaolu ;
Weber, Rodney J. ;
Yan, Bo ;
Russell, Armistead G. ;
Edgerton, Eric S. ;
Wang, Xinming .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (14) :5171-5176
[10]   Contemporary or Fossil Origin: Split of Estimated Secondary Organic Carbon in the Southeastern United States [J].
Ding, Xiang ;
Zheng, Mei ;
Edgerton, Eric S. ;
Jansen, John J. ;
Wang, Xinming .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (24) :9122-9128