Annual emissions of mercury to the atmosphere from natural sources in Nevada and California

被引:74
作者
Coolbaugh, MF
Gustin, MS
Rytuba, JJ
机构
[1] Univ Nevada, Dept Environm & Resources Sci, Reno, NV 89557 USA
[2] Univ Nevada, Dept Geol Sci, Reno, NV 89557 USA
[3] US Geol Survey, Menlo Pk, CA 94025 USA
来源
ENVIRONMENTAL GEOLOGY | 2002年 / 42卷 / 04期
关键词
atmospheric mercury; geographic information system; natural sources; scaling;
D O I
10.1007/s00254-002-0557-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The impact of natural source emissions on atmospheric mercury concentrations and the bio-geochemical cycle of mercury is not known. To begin to assess this impact, mercury emissions to the atmosphere were scaled up for three areas naturally enriched in mercury: the Steamboat Springs geo-thermal area, Nevada, the New Idria mercury mining district, California, and the Medicine Lake volcano, California. Data used to scale up area emissions included mercury fluxes, measured in-situ using field flux chambers, from undisturbed and disturbed geologic substrates, and relationships between mercury emissions and geologic rock types, soil mercury concentrations, and surface heat flux. At select locations mercury fluxes were measured for 24 h and the data were used to adjust fluxes measured at different times of the day to give an average daily flux. This adjustment minimized daily temporal variability, which is observed for mercury flux because of light and temperature effects. Area emissions were scaled spatially and temporally with GIS software. Measured fluxes ranged from 0.3 to approximately 50 ng m(-2) h(-1) at undisturbed sites devoid of mercury mineralization, and to greater than 10,000 ng m(-2) h(-1) from substrates that were in areas of mercury mining. Area-averaged fluxes calculated for bare soil at Steamboat Springs, New Idria, and Medicine Lake of 181, 9.2, and 2 ng m(-2) h(-1), respectively, are greater than fluxes previously ascribed to natural non-point sources, indicating that these sources may be more significant contributors of mercury to the atmosphere than previously realized.
引用
收藏
页码:338 / 349
页数:12
相关论文
共 30 条
[1]   DETERMINATION OF VOLATILE MERCURY SPECIES AT THE PICOGRAM LEVEL BY LOW-TEMPERATURE GAS-CHROMATOGRAPHY WITH COLD-VAPOR ATOMIC FLUORESCENCE DETECTION [J].
BLOOM, N ;
FITZGERALD, WF .
ANALYTICA CHIMICA ACTA, 1988, 208 (1-2) :151-161
[2]  
BRADLEY WM, 1918, CALIF STATE MINING B, V78, P396
[3]  
BRANNOCK WW, 1948, NEVADA T AM GEOPHYS, V29, P211
[4]   Application of a Teflon™ dynamic flux chamber for quantifying soil mercury flux:: Tests and results over background soil [J].
Carpi, A ;
Lindberg, SE .
ATMOSPHERIC ENVIRONMENT, 1998, 32 (05) :873-882
[5]   MERCURY STACK EMISSIONS FROM US ELECTRIC UTILITY POWER-PLANTS [J].
CHU, P ;
PORCELLA, DB .
WATER AIR AND SOIL POLLUTION, 1995, 80 (1-4) :135-144
[6]  
Coolbaugh M., 2000, P 14 THEM C APPL GEO, P623
[7]   POST-11,000-YEAR VOLCANISM AT MEDICINE LAKE VOLCANO, CASCADE RANGE, NORTHERN CALIFORNIA [J].
DONNELLYNOLAN, JM ;
CHAMPION, DE ;
MILLER, CD ;
GROVE, TL ;
TRIMBLE, DA .
JOURNAL OF GEOPHYSICAL RESEARCH-SOLID EARTH AND PLANETS, 1990, 95 (B12) :19693-19704
[8]  
DONNELLYNOLAN JM, 1993, SOC EC GEOLOGISTS GU, V16
[9]   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
[10]  
Eckel E. B., 1946, CALIF J MINES GEOL, V42, P81