Local and regional air pollution in Ireland during an intensive aerosol measurement campaign

被引:6
|
作者
Ceburnis, D
Yin, J
Allen, AG
Jennings, SG
Harrison, RM
Wright, E
Fitzpatrick, M
Healy, T
Barry, E
机构
[1] Natl Univ Ireland Univ Coll Galway, Dept Expt Phys, Atmospher Res Grp, Galway, Ireland
[2] Univ Birmingham, Sch Geog Earth & Environm Sci, Birmingham B15 2TT, W Midlands, England
[3] Dublin City Council, Community & Environm Dept, Atmospher & Noise Unit, Dublin, Ireland
[4] Cork City Council, Environm Lab, Cork, Ireland
来源
JOURNAL OF ENVIRONMENTAL MONITORING | 2006年 / 8卷 / 04期
关键词
D O I
10.1039/b516029d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An intensive two month measurement campaign has been performed during a two year study of major component composition of urban PM10 and PM2.5 in Ireland ( J. Yin, A. G. Allen, R. M. Harrison, S. G. Jennings, E. Wright, M. Fitzpatrick, T. Healy, E. Barry, D. Ceburnis and D. McCusker, Atmos. Res., 2005, 78( 3 - 4), 149 - 165). Measurements included size- segregated mass, soluble ions, elemental carbon ( EC) distributions,. ne and coarse fraction organic carbon ( OC) and major gases along with standard meteorological measurements. The study revealed that urban emissions in Ireland had mainly a local character and therefore were confined within a limited area of 20 - 30 km radius, without significantly affecting regional air quality. Gaseous ;measurements have shown that urban emissions in Ireland had clear, but fairly limited influence on the regional air quality due to favorable mixing conditions at higher wind speeds, in particular from the western sector. Size- segregated mass and chemical measurements revealed a clear demarcation size between accumulation and coarse modes at about 0.8 mm which was constant at all sites. Carbonaceous compounds at the urban site accounted for up to 90% of the particle mass in a size range of 0.066 - 0.61 mm. Nss SO42- concentrations in PM2.5 were only slightly higher at the urban site compared to the rural or coastal sites, while NO3- and NH4+ concentrations were similar at the urban and coastal sites, but were a factor of 2 to 3 higher than at the rural site. OC was highly variable between the sites and revealed clear seasonal differences. Natural or biogenic OC component accounted for < 10% in winter and up to 30% in summer of the PM2.5 OC at urban sites. A contribution of biogenic OC component to PM2.5 OC mass at rural site was dominant.
引用
收藏
页码:479 / 487
页数:9
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