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Relationship between the loading rate of inorganic mercury to aquatic ecosystems and dissolved gaseous mercury production and evasion
Authors:Poulain Alexandre J  Orihel Diane M  Amyot Marc  Paterson Michael J  Hintelmann Holger  Southworth George R
Institution:

aDépartement de Sciences Biologiques, Université de Montréal, C.P. 6128, Succursale Centre-Ville, Pavillon Marie-Victorin, Montréal, QC, Canada H3C 3J7

bClayton H. Riddell Faculty of Environment, Earth and Resources, University of Manitoba, Winnipeg, MB, Canada R3T 2N2

cFreshwater Institute, Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, MB, Canada R3T 2N6

dDepartment of Chemistry, Trent University, 1600 West Bank Drive, Peterborough, ON, Canada K9J 7B8

eEnvironmental Sciences Division, Oak Ridge National Laboratory, Building 1505, P.O. Box 2008 MS6036, Oak Ridge, TN 37831-6036, United States

Abstract:The purpose of our study was to test the hypothesis that dissolved gaseous mercury (DGM) production and evasion is directly proportional to the loading rate of inorganic mercury Hg(II)] to aquatic ecosystems. We simulated different rates of atmospheric mercury deposition in 10-m diameter mesocosms in a boreal lake by adding multiple additions of Hg(II) enriched with a stable mercury isotope (202Hg). We measured DGM concentrations in surface waters and estimated evasion rates using the thin-film gas exchange model and mass transfer coefficients derived from sulfur hexafluoride (SF6) additions. The additions of Hg(II) stimulated DGM production, indicating that newly added Hg(II) was highly reactive. Concentrations of DGM derived from the experimental Hg(II) additions (“spike DGM”) were directly proportional to the rate of Hg(II) loading to the mesocosms. Spike DGM concentrations averaged 0.15, 0.48 and 0.94 ng l?1 in mesocosms loaded at 7.1, 14.2, and 35.5 μg Hg m?2 yr?1, respectively. The evasion rates of spike DGM from these mesocosms averaged 4.2, 17.2, and 22.3 ng m?2 h?1, respectively. The percentage of Hg(II) added to the mesocosms that was lost to the atmosphere was substantial (33–59% over 8 weeks) and was unrelated to the rate of Hg(II) loading. We conclude that changes in atmospheric mercury deposition to aquatic ecosystems will not change the relative proportion of mercury recycled to the atmosphere.
Keywords:Dissolved gaseous mercury  Evasion  Atmospheric deposition  Stable isotope  Sulfur hexafluoride  METAALICUS
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