Export of atmospheric mercury from Asia. Jaffe, D., Prestbo, E., Swartzendruber, P., Weiss-Penzias, P., Kato, S., Takami, A., Hatakeyama, S., & Kajii, Y. Atmospheric Environment, 39(17):3029-3038, 2005.
Export of atmospheric mercury from Asia [link]Website  abstract   bibtex   
Emissions inventories indicate that Asian Hg sources are more than 50% of the global anthropogenic total. However, few measurements have been made to verify these large emissions. In this paper, we report on measurements of mercury from two sites during spring 2004 which received Asian outflow: Hedo Station, Okinawa (HSO), Japan and the Mt. Bachelor Observatory (MBO) in central Oregon, USA. At both sites, export of atmospheric mercury from China and East Asia was verified by the observations and meteorological data. The mean Hg-0 concentration we observed at HSO was 2.04 ng m(-3), which is significantly higher than the global background. Measurements of reactive gaseous mercury and particulate mercury at HSO found relatively little outflow of these compounds from Asia, generally less than 3% of the total mercury. By examining the correlation of Hg-0 to carbon monoxide during outflow events, we have derived an enhancement ratio, which should reflect the ratio of these compounds in the source region. During outflow from Asia, the mean Hg-0/CO molar enhancement ratio we observed at HSO was 6.2 x 10(-7), which is nearly twice the expected ratio based on emissions estimates from China. During one episode of long-range transport from Asia to the MBO, we found a very similar ratio of Hg-0/CO to that observed at HSO and a similar ratio was also reported by Friedli et al. (2004, Journal of Geophysical Research 109, D19 S25) downwind of Shanghai. Thus the ratio of Hg-0/CO appears to be a good tracer of Asian industrial outflow. Using the Hg-0/CO ratio and a recent inventory for CO emissions, we calculate Hg-0 emissions from Asia of 1460 metric tons year(-1), which is nearly two times the value in the Pacyna et al. (2003, Global mercury emissions. Presented at Long-Range Transport Workshop, Ann Arbor, MI, September 2003) inventory. Several hypotheses are proposed to explain this discrepancy, including an underestimation of the Chinese industrial Hg-0 emissions, natural sources, significant re-emissions of previously deposited Hg and/or a higher ratio of Hg-0/total Hg in the outflow from Asia than in the emission inventory. (c) 2005 Elsevier Ltd. All rights reserved.
@article{
 title = {Export of atmospheric mercury from Asia},
 type = {article},
 year = {2005},
 keywords = {Asia,Trans-pacific transport,air,anthropogenic sources,carbon monoxide,carbon-monoxide,deposition,elemental mercury,emissions,gaseous mercury,mercury,northeast pacific,ozone,pollution},
 pages = {3029-3038},
 volume = {39},
 websites = {<Go to ISI>://000230123900004},
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 notes = {Article<br/>1352-2310},
 abstract = {Emissions inventories indicate that Asian Hg sources are more than 50% of the global anthropogenic total. However, few measurements have been made to verify these large emissions. In this paper, we report on measurements of mercury from two sites during spring 2004 which received Asian outflow: Hedo Station, Okinawa (HSO), Japan and the Mt. Bachelor Observatory (MBO) in central Oregon, USA. At both sites, export of atmospheric mercury from China and East Asia was verified by the observations and meteorological data. The mean Hg-0 concentration we observed at HSO was 2.04 ng m(-3), which is significantly higher than the global background. Measurements of reactive gaseous mercury and particulate mercury at HSO found relatively little outflow of these compounds from Asia, generally less than 3% of the total mercury. By examining the correlation of Hg-0 to carbon monoxide during outflow events, we have derived an enhancement ratio, which should reflect the ratio of these compounds in the source region. During outflow from Asia, the mean Hg-0/CO molar enhancement ratio we observed at HSO was 6.2 x 10(-7), which is nearly twice the expected ratio based on emissions estimates from China. During one episode of long-range transport from Asia to the MBO, we found a very similar ratio of Hg-0/CO to that observed at HSO and a similar ratio was also reported by Friedli et al. (2004, Journal of Geophysical Research 109, D19 S25) downwind of Shanghai. Thus the ratio of Hg-0/CO appears to be a good tracer of Asian industrial outflow. Using the Hg-0/CO ratio and a recent inventory for CO emissions, we calculate Hg-0 emissions from Asia of 1460 metric tons year(-1), which is nearly two times the value in the Pacyna et al. (2003, Global mercury emissions. Presented at Long-Range Transport Workshop, Ann Arbor, MI, September 2003) inventory. Several hypotheses are proposed to explain this discrepancy, including an underestimation of the Chinese industrial Hg-0 emissions, natural sources, significant re-emissions of previously deposited Hg and/or a higher ratio of Hg-0/total Hg in the outflow from Asia than in the emission inventory. (c) 2005 Elsevier Ltd. All rights reserved.},
 bibtype = {article},
 author = {Jaffe, D and Prestbo, E and Swartzendruber, P and Weiss-Penzias, P and Kato, S and Takami, A and Hatakeyama, S and Kajii, Y},
 journal = {Atmospheric Environment},
 number = {17}
}
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