Trend and variability of total gaseous mercury (TGM) in the state of Connecticut, USA during 1997-1999

被引:9
作者
Chen, H
Yang, XS [1 ]
Perkins, C
机构
[1] Univ Connecticut, Dept Nat Resources Management & Engn, Storrs, CT 06268 USA
[2] Univ Connecticut, Environm Res Inst, Storrs, CT USA
关键词
Connecticut; land use; long-range transport; site location; total gaseous mercury;
D O I
10.1023/B:WATE.0000009900.11597.95
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A statewide total gaseous mercury (TGM) monitoring campaign was conducted from January 1997 to December 1999 in the State of Connecticut, U. S. A. Eight monitoring sites with different characteristics of geographical location ( coastal vs. interior) and land use ( rural vs. urban) were included in the monitoring program. Statistical procedures were utilized to evaluate the temporal trend and spatial distribution of the TGM concentration in the State, and the influence of long-range transport from non-local sources. The statewide mean TGM concentration was 2.08 ng m(-3). The annual mean concentration had no significant differences among the three years of measurements for all the sites. Weak seasonal variations were detected in the State with higher ambient TGM concentration found in warmer seasons. Urban areas in general had higher TGM concentrations than rural areas. The effect of site location of the monitoring sites on TGM concentration was interacted with land use characteristics. Waterbury site with extremely high concentration measurements was the major cause for this interaction. The long-range transport of TGM from remote sources showed an important influence on local ambient concentrations, by explaining over 45% of the total variance of the ambient TGMconcentration for most sites. Local sources were responsible for the extremely high TGMconcentration in the Waterbury site. The TGM concentrations at Voluntown, Hammonasset and Avery Point in southeast Connecticut were likely to be affected by some local sources.
引用
收藏
页码:103 / 116
页数:14
相关论文
共 27 条
[1]  
[Anonymous], EPA453R98004A
[2]   Large scale mercury and trace element measurements in the Amazon basin [J].
Artaxo, P ;
de Campos, RC ;
Fernandes, ET ;
Martins, JV ;
Xiao, ZF ;
Lindqvist, O ;
Fernández-Jiménez, MT ;
Maenhaut, W .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (24) :4085-4096
[3]  
Axelrad DA., 1999, ENV SCI POLICY, V2, P397, DOI DOI 10.1016/S1462-9011(99)00036-2
[4]  
CARLEY RJ, 2001, UNPUB CONNECTICUT AT
[5]   International field intercomparison measurements of atmospheric mercury species at Mace Head, Ireland [J].
Ebinghaus, R ;
Jennings, SG ;
Schroeder, WH ;
Berg, T ;
Donaghy, T ;
Guentzel, J ;
Kenny, C ;
Kock, HH ;
Kvietkus, K ;
Landing, W ;
Mühleck, T ;
Munthe, J ;
Prestbo, EM ;
Schneeberger, D ;
Slemr, F ;
Sommar, J ;
Urba, A ;
Wallschläger, D ;
Xiao, Z .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (18) :3063-3073
[6]  
ILYIN L, 2002, 32002 EMEP COOP PROG
[7]   LONG-TERM CHANGES IN CONCENTRATION AND DEPOSITION OF ATMOSPHERIC MERCURY OVER SCANDINAVIA [J].
IVERFELDT, A ;
MUNTHE, J ;
BROSSET, C ;
PACYNA, J .
WATER AIR AND SOIL POLLUTION, 1995, 80 (1-4) :227-233
[8]   Dispersion of pollutants in street canyon under traffic induced flow and turbulence [J].
Jicha, M ;
Pospisil, J ;
Katolicky, J .
ENVIRONMENTAL MONITORING AND ASSESSMENT, 2000, 65 (1-2) :343-351
[9]   Total gaseous mercury concentration and flux over a coastal saltmarsh vegetation in Connecticut, USA [J].
Lee, X ;
Benoit, G ;
Hu, XZ .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (24) :4205-4213
[10]  
Lin CJ, 2001, ATMOS ENVIRON, V35, P1141