DRY DEPOSITION OF SEMIVOLATILE ORGANIC-COMPOUNDS TO LAKE-MICHIGAN

被引:60
作者
PIRRONE, N
KEELER, GJ
HOLSEN, TM
机构
[1] UNIV MICHIGAN,AIR QUAL LAB,ANN ARBOR,MI 48109
[2] IIT,PRITZKER DEPT ENVIRONM ENGN,CHICAGO,IL 60616
关键词
D O I
10.1021/es00008a035
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Lake Michigan Urban Air Toxics Study (LMUATS) was carried out from July 8 to August 9, 1991, in the southern Lake Michigan basin. The investigation was the first aimed at assessing the impact of the Chicago/Gary urban plume on the deposition of hazardous air pollutants (HAPs) to Lake Michigan. The concentrations of a large number of semivolatile organic compounds (SOCs) were measured at four locations (Kankakee, IL; Chicago, IL; over Lake Michigan onboard the R/V Laurentian; and South Haven, MI). These sites were chosen as they are often linked by air mass transport with air masses reaching South Haven, after passing through Chicago, often having an over-water path to the downwind site. The University of Michigan R/V Laurentian was also deployed off-shore of Chicago to measure the concentrations of HAPs as they were transported out over the water. A hybrid-receptor deposition (HRD) modeling approach, which utilized measured atmospheric concentrations at a receptor site together with observed meteorological data in a lagrangian dispersion modeling framework, was used to estimate both gas exchange across the air-water interface and particle dry deposition of SOCs to Lake Michigan. The atmospheric concentrations of selected pesticides, PCBs, and PAHs measured during the LMUATS were used as input to the HRD model. The comparison between the measured and calculated ambient concentrations gives reasonable results with measured/calculated concentration ratios in the range of 0.3-1.9 for pesticides, 0.9-2.6 for PCBs, and 0.5-3.8 for PAHs. A comparison of deposition fluxes obtained in this study with those found in lite rature reveals large differences far some compounds, especially for those that are primarily in the particle phase. This finding suggests that assuming constant values of critical parameters controlling the transfer processes of gaseous and particulate SOCs from the atmosphere to the water surface may result in estimates with large uncertainties.
引用
收藏
页码:2123 / 2132
页数:10
相关论文
共 44 条
[31]   GAS-EXCHANGE OF HEXACHLOROCYCLOHEXANE IN THE GREAT-LAKES [J].
MCCONNELL, LL ;
COTHAM, WE ;
BIDLEMAN, TF .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (07) :1304-1311
[32]  
MCVEETY BD, 1986, THESIS U MINNESOTA
[33]  
NOLL KE, 1992, PRECIPITATION SCAVEN, V2, P683
[34]   AN ABSORPTION-MODEL OF THE GAS AEROSOL PARTITIONING INVOLVED IN THE FORMATION OF SECONDARY ORGANIC AEROSOL [J].
PANKOW, JF .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (02) :189-193
[35]   AN ABSORPTION-MODEL OF GAS-PARTICLE PARTITIONING OF ORGANIC-COMPOUNDS IN THE ATMOSPHERE [J].
PANKOW, JF .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (02) :185-188
[37]   DRY DEPOSITION OF TRACE-ELEMENTS TO LAKE-MICHIGAN - A HYBRID-RECEPTOR DEPOSITION MODELING APPROACH [J].
PIRRONE, N ;
KEELER, GJ ;
HOLSEN, TM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (08) :2112-2122
[38]   PREDICTIONS FOR PARTICLE DEPOSITION ON NATURAL-WATERS [J].
SLINN, SA ;
SLINN, WGN .
ATMOSPHERIC ENVIRONMENT, 1980, 14 (09) :1013-1016
[39]  
Slinn W.G.N., 1983, PRECIPITATION SCAVEN
[40]  
STRACHAN WMJ, 1988, 1986 P WORKSH EST AT