Modeling the atmospheric transport and deposition of mercury to the Great Lakes

被引:123
作者
Cohen, M
Artz, R
Draxler, R
Miller, P
Poissant, L
Niemi, D
Ratté, D
Deslauriers, M
Duval, R
Laurin, R
Slotnick, J
Nettesheim, T
McDonald, J
机构
[1] NOAA, Air Resources Lab, Silver Spring, MD 20910 USA
[2] Commiss Environm Cooperat, Montreal, PQ, Canada
[3] Environm Canada, Meteorol Serv Canada, Atmospher Tox Proc Serv, Montreal, PQ, Canada
[4] Environm Canada, Pollutant Data Branch, Hull, PQ, Canada
[5] Ontario Minist Environm, Environm Monitoring & Reporting Branch, Toronto, ON, Canada
[6] Univ Calif Berkeley, Berkeley, CA 94720 USA
[7] US EPA, Great Lakes Natl Program Office, Chicago, IL USA
[8] Int Joint Commiss, Windsor, ON N9A 6T3, Canada
关键词
mercury; atmospheric deposition; Great Lakes; source-receptor modeling; emissions;
D O I
10.1016/j.envres.2003.11.007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A special version of the NOAA HYSPLIT-4 model has been developed and used to estimate the atmospheric fate and transport of mercury in a North American modeling domain. Spatial and chemical interpolation procedures were used to expand the modeling results and provide estimates of the contribution of each source in a 1996 anthropogenic US/Canadian emissions inventory to atmospheric mercury deposition to the Great Lakes. While there are uncertainties in the emissions inventories and ambient data suitable for model evaluation are scarce, model results were found to be reasonably consistent with wet deposition measurements in the Great Lakes region and with independent measurement-based estimates of deposition to Lake Michigan. Sources up to 2000 km from the Great Lakes contributed significant amounts of mercury through atmospheric transport and deposition. While there were significant contributions from incineration and metallurgical sources, coal combustion was generally found to be the largest contributor to atmospheric mercury deposition to the Great Lakes. Published by Elsevier Inc.
引用
收藏
页码:247 / 265
页数:19
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