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Detailed Reference Information |
Lu, J.Y., Schroeder, W.H., Barrie, L.A., Steffen, A., Welch, H.E., Martin, K., Lockhart, L., Hunt, R.V., Boila, G. and Richter, A. (2001). Magnification of atmospheric mercury deposition to polar regions in springtime: The link to tropospheric ozone depletion chemistry. Geophysical Research Letters 28: doi: 10.1029/2000GL012603. issn: 0094-8276. |
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Mercury-in the chemical/physical forms present in the biosphere-is a persistent, toxic, bioaccumulative pollutant that is dispersed throughout the environment on a global scale, mainly via the atmosphere. It is among the heavy metals for which the natural biogeochemical cycle has been perturbed by a wide range of human activities, including fossil-fuel combustion and waste incineration. Results of our recent measurements of gaseous elemental mercury (GEM), as well as total particulate-phase mercury (TPM) concentrations in Arctic air, 'total Hg' concentrations in Arctic snow, and tropospheric BrO concentrations from an earth-orbiting-satellite platform are presented and discussed. Findings of our research, and the conclusions derived therefrom, are important for environmental protection as well as the health and well-being of aboriginal people in Arctic circumpolar nations. ¿ 2001 American Geophysical Union |
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Abstract |
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Keywords
Atmospheric Composition and Structure, Biosphere/atmosphere interactions, Atmospheric Composition and Structure, Troposphere—constituent transport and chemistry, Meteorology and Atmospheric Dynamics, Boundary layer processes |
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Publisher
American Geophysical Union 2000 Florida Avenue N.W. Washington, D.C. 20009-1277 USA 1-202-462-6900 1-202-328-0566 service@agu.org |
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