Atmos. Chem. Phys., 13, 7007-7021, 2013
www.atmos-chem-phys.net/13/7007/2013/
doi:10.5194/acp-13-7007-2013
© Author(s) 2013. This work is distributed
under the Creative Commons Attribution 3.0 License.
Atmospheric mercury over sea ice during the OASIS-2009 campaign
A. Steffen1,2, J. Bottenheim1, A. Cole1, T. A. Douglas3, R. Ebinghaus2,4, U. Friess5, S. Netcheva1, S. Nghiem6, H. Sihler5, and R. Staebler1
1Air Quality Processes Research Section, Environment Canada, 4905 Dufferin St., Toronto, Ontario M3H 5T4, Canada,
2Leuphana University Lüneburg, Institute of Sustainable & Environmental Chemistry (ISEC), Scharnhorststr. 1/13, 21335 Lüneburg, Germany
3US Army Cold Regions Research & Engineering Laboratory, Fort Wainwright, Alaska 99703, USA
4Helmholtz-Zentrum Geesthacht, Institute of Coastal Research, Department for Environmental Chemistry, Max-Planck-Str. 1, 21502 Geesthacht, Germany
5Institute of Environmental Physics, University of Heidelberg, Im Neuenheimer Feld 229, 69120 Heidelberg, Germany
6Jet Propulsion Laboratory, California Institute of Technology, Pasadena, California, USA

Abstract. Measurements of gaseous elemental mercury (GEM), reactive gaseous mercury (RGM) and particulate mercury (PHg) were collected on the Beaufort Sea ice near Barrow, Alaska, in March 2009 as part of the Ocean-Atmosphere-Sea Ice-Snowpack (OASIS) and OASIS-Canada International Polar Year programmes. These results represent the first atmospheric mercury speciation measurements collected on the sea ice. Concentrations of PHg averaged 393.5 pg m−3 (range 47.1–900.1 pg m−3) and RGM concentrations averaged 30.1 pg m−3 (range 3.5–105.4 pg m−3) during the two-week-long study. The mean concentration of GEM during the study was 0.59 ng m−3 (range 0.01–1.51 ng m−3) and was depleted compared to annual Arctic ambient boundary layer concentrations. It is shown that when ozone (O3) and bromine oxide (BrO) chemistry were active there is a positive linear relationship between GEM and O3, a negative one between PHg and O3, a positive correlation between RGM and BrO, and none between RGM and O3. For the first time, GEM was measured simultaneously over the tundra and the sea ice. The results show a significant difference in the magnitude of the emission of GEM from the two locations, with significantly higher emission over the tundra. Elevated chloride levels in snow over sea ice are proposed to be the cause of lower GEM emissions over the sea ice because chloride has been shown to suppress photoreduction processes of RGM to GEM in snow. Since the snowpack on sea ice retains more mercury than inland snow, current models of the Arctic mercury cycle may greatly underestimate atmospheric deposition fluxes because they are based predominantly on land-based measurements. Land-based measurements of atmospheric mercury deposition may also underestimate the impacts of sea ice changes on the mercury cycle in the Arctic. The predicted changes in sea ice conditions and a more saline future snowpack in the Arctic could enhance retention of atmospherically deposited mercury and increase the amount of mercury entering the Arctic Ocean and coastal ecosystems.

Citation: Steffen, A., Bottenheim, J., Cole, A., Douglas, T. A., Ebinghaus, R., Friess, U., Netcheva, S., Nghiem, S., Sihler, H., and Staebler, R.: Atmospheric mercury over sea ice during the OASIS-2009 campaign, Atmos. Chem. Phys., 13, 7007-7021, doi:10.5194/acp-13-7007-2013, 2013.
 
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