ATMOSPHERIC SOURCES, TRANSPORT AND DEPOSITION OF MERCURY IN MICHIGAN - 2 YEARS OF EVENT PRECIPITATION

被引:77
作者
HOYER, M
BURKE, J
KEELER, G
机构
[1] Air Quality Laboratory, The University of Michigan, Ann Arbor, 48109-2029, MI
关键词
MERCURY; WET DEPOSITION; PRECIPITATION; TRACE ELEMENTS; REGIONAL TRANSPORT; TRAJECTORIES;
D O I
10.1007/BF01189668
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
To assess the sources, transport and deposition of atmospheric mercury (Hg) in Michigan a multi-site network was implemented in which Hg concentrations in event precipitation and ambient samples (vapor and particulate phases) were determined. Results from the analysis of 2 years of event precipitation samples for Hg are reported here. The volume-weighted average Hg concentration in precipitation was 7.9, 10.8 and 10.2 ng/L for the Pellston South Haven and Dexter sites, respectively. Yearly wet deposition of Hg for 1992-93 and 1993-94 was 5.8 and 5.5 mu g/m(2) at Pellston, 9.5 and 12.7 mu g/m(2) at South Haven and 8.7 and 9.1 mu g/m(2) at Dexter. A. spatial gradient in both the Hg concentration and wet deposition was observed Northern Michigan received almost half the deposition of Hg recorded at the southern Michigan sites. The concentration of Hg in precipitation exhibited a strong seasonal behavior with low values of 1.0 to 2.0 ng/L in winter and maximum values greater than 40 ng/L in summer. The spring, summer and autumn precipitation accounted for 89 to 91% of the total yearly Hg deposition Mixed-layer back trajectories were calculated for each precipitation event to investigate the meteorological history and transport from potential Hg source regions. Elevated Hg concentrations were observed with air mass transport from the west southwest south, and southeast. At each of the sites precipitation events for which the Hg condentration was in the 90th and 10th percentile were analyzed for trace elements by ICP-MS to investigate source impacts.
引用
收藏
页码:199 / 208
页数:10
相关论文
共 27 条
  • [1] THE CHEMICAL FRACTIONATION OF ATMOSPHERIC AEROSOL AS A RESULT OF SNOW CRYSTAL-FORMATION AND GROWTH
    BORYS, RD
    HINDMAN, EE
    DEMOTT, PJ
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1988, 7 (03) : 213 - 239
  • [2] THE BEHAVIOR OF MERCURY IN THE PHYSICAL-ENVIRONMENT
    BROSSET, C
    [J]. WATER AIR AND SOIL POLLUTION, 1987, 34 (02) : 145 - 166
  • [3] WET DEPOSITION OF MERCURY AND AMBIENT MERCURY CONCENTRATIONS AT A SITE IN THE LAKE CHAMPLAIN BASIN
    BURKE, J
    HOYER, M
    KEELER, G
    SCHERBATSKOY, T
    [J]. WATER AIR AND SOIL POLLUTION, 1995, 80 (1-4) : 353 - 362
  • [4] ATMOSPHERIC CYCLING AND AIR-WATER EXCHANGE OF MERCURY OVER MIDCONTINENTAL LACUSTRINE REGIONS
    FITZGERALD, WF
    MASON, RP
    VANDAL, GM
    [J]. WATER AIR AND SOIL POLLUTION, 1991, 56 : 745 - 767
  • [5] SUB-NANOGRAM DETERMINATION OF MERCURY BY 2-STAGE GOLD AMALGAMATION AND GAS-PHASE DETECTION APPLIED TO ATMOSPHERIC ANALYSIS
    FITZGERALD, WF
    GILL, GA
    [J]. ANALYTICAL CHEMISTRY, 1979, 51 (11) : 1714 - 1720
  • [6] AIRBORNE MERCURY IN PRECIPITATION IN THE LAKE-SUPERIOR REGION
    GLASS, GE
    LEONARD, EN
    CHAN, WH
    ORR, DB
    [J]. JOURNAL OF GREAT LAKES RESEARCH, 1986, 12 (01) : 37 - 51
  • [7] HEFFLER JL, 1980, NOAA ERL ARL81 TECHN, P17
  • [8] HOYER M, 1993, 9TH P INT C HEAV MET, P332
  • [9] HOYER ME, 1994, UNPUB ATMOS ENV
  • [10] HOYER MH, 1994, UNPUB ENV SCI TECHNO