Articles | Volume 14, issue 5
Atmos. Chem. Phys., 14, 2219–2231, 2014
Atmos. Chem. Phys., 14, 2219–2231, 2014

Research article 03 Mar 2014

Research article | 03 Mar 2014

Atmospheric mercury speciation and mercury in snow over time at Alert, Canada

A. Steffen1,2, J. Bottenheim1, A. Cole1, R. Ebinghaus2,3, G. Lawson4, and W. R. Leaitch1 A. Steffen et al.
  • 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
  • 3Helmholtz-Zentrum Geesthacht, Institute of Coastal Research, Department for Environmental Chemistry,Max-Planck-Str. 1, 21502 Geesthacht, Germany
  • 4Environment Canada, Science and Technology Branch, 867 Lakeshore Rd, Burlington, Ontario, L7R 4A6, Canada

Abstract. Ten years of atmospheric mercury speciation data and 14 years of mercury in snow data from Alert, Nunavut, Canada, are examined. The speciation data, collected from 2002 to 2011, includes gaseous elemental mercury (GEM), particulate mercury (PHg) and reactive gaseous mercury (RGM). During the winter-spring period of atmospheric mercury depletion events (AMDEs), when GEM is close to being completely depleted from the air, the concentration of both PHg and RGM rise significantly. During this period, the median concentrations for PHg is 28.2 pgm−3 and RGM is 23.9 pgm−3, from March to June, in comparison to the annual median concentrations of 11.3 and 3.2 pgm−3 for PHg and RGM, respectively. In each of the ten years of sampling, the concentration of PHg increases steadily from January through March and is higher than the concentration of RGM. This pattern begins to change in April when the levels of PHg peak and RGM begin to increase. In May, the high PHg and low RGM concentration regime observed in the early spring undergoes a transition to a regime with higher RGM and much lower PHg concentrations. The higher RGM concentration continues into June. The transition is driven by the atmospheric conditions of air temperature and particle availability. Firstly, a high ratio of the concentrations of PHg to RGM is reported at low temperatures which suggests that oxidized gaseous mercury partitions to available particles to form PHg. Prior to the transition, the median air temperature is −24.8 °C and after the transition the median air temperature is −5.8 °C. Secondly, the high PHg concentrations occur in the spring when high particle concentrations are present. The high particle concentrations are principally due to Arctic haze and sea salts. In the snow, the concentrations of mercury peak in May for all years. Springtime deposition of total mercury to the snow at Alert peaks in May when atmospheric conditions favour higher levels of RGM. Therefore, the conditions in the atmosphere directly impact when the highest amount of mercury will be deposited to the snow during the Arctic spring.

Final-revised paper