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Fate of Elemental Mercury in the Arctic during Atmospheric Mercury Depletion Episodes and the Load of Atmospheric Mercury to the Arctic

Authors :
Michael Evan Goodsite
Bjarne Bruun Jensen
Peter Wåhlin
Gerald Geernaert
Jesper H. Christensen
Niels Z. Heidam
Henrik Skov
Source :
Skov, H, Christensen, J, Goodsite, M, Heidam, N Z, Jensen, B, Wåhlin, P & Geernaert, G 2004, ' Fate of Elemental Mercury in the Arctic during Atmospheric Mercury Depletion Episodes and the Load of Atmospheric Mercury to the Arctic ', Environmental Science & Technology (Washington), vol. 38, no. 8, pp. 2373-2382 ., Aarhus University, Skov, H, Christensen, J H, Goodsite, M E, Heidam, N Z, Jensen, B, Wahlin, P & Geernaert, G 2004, ' Fate of elemental mercury in the arctic during atmospheric mercury depletion episodes and the load of atmospheric mercury to the arctic ', Environmental Science & Technology (Washington), vol. 38, no. 8 ., University of Southern Denmark
Publication Year :
2004
Publisher :
American Chemical Society (ACS), 2004.

Abstract

Atmospheric mercury depletion episodes (AMDEs) were studied at Station Nord, Northeast Greenland, 81 degrees 36' N, 16 degrees 40' W, during the Arctic Spring. Gaseous elemental mercury (GEM) and ozone were measured starting from 1998 and 1999, respectively, until August 2002. GEM was measured with a TEKRAN 2735A automatic mercury analyzer based on preconcentration of mercury on a gold trap followed by detection using fluorescence spectroscopy. Ozone was measured by UV absorption. A scatter plot of GEM and ozone concentrations confirmed that also at Station Nord GEM and ozone are linearly correlated during AMDEs. The relationship between ozone and GEM is further investigated in this paper using basic reaction kinetics (i.e., Cl, ClO, Br, and BrO have been suggested as reactants for GEM). The analyses in this paper show that GEM in the Arctic troposphere most probably reacts with Br. On the basis of the experimental results of this paper and results from the literature, a simple parametrization for AMDE was included into the Danish Eulerian Hemispheric Model (DEHM). In the model, GEM is converted linearly to reactive gaseous mercury (RGM) over sea ice with temperature below -4 degrees C with a lifetime of 3 or 10 h. The new AMDE parametrization was used together with the general parametrization of mercury chemistry [Petersen, G.; Munthe, J.; Pleijel, K.; Bloxam, R.; Vinod Kumar, A. Atmos. Environ. 1998, 32, 829-843]. The obtained model results were compared with measurements of GEM at Station Nord. There was good agreement between the start and general features periods with AMDEs, although the model could not reproduce the fast concentration changes, and the correlation between modeled and measured values decreased from 2000 to 2001 and further in 2002. The modeled RGM concentrations over the Arctic in 2000 were found to agree well with the temporal and geographical variability of the boundary column of monthly average BrO observed by the GOME satellite. Scenario calculations were performed with and without AMDEs. For the area north of the Polar Circle, the mercury deposition increases from 89 tons/year for calculations without an AMDE to 208 tons/year with the AMDE. The 208 tons/year represent an upper limit for the mercury load to the Artic.

Details

ISSN :
15205851 and 0013936X
Volume :
38
Database :
OpenAIRE
Journal :
Environmental Science & Technology
Accession number :
edsair.doi.dedup.....dc4f7ce434a9f18f0ab40307d670a65b
Full Text :
https://doi.org/10.1021/es030080h