1Science and Technology Program, University of Washington-Bothell, Bothell, WA, USA
2Air Quality Research, Finnish Meteorological Institute, Helsinki, Finland
3Department of Atmospheric Sciences, University of Washington, Seattle, WA, USA
Received: 03 Nov 2012 – Published in Atmos. Chem. Phys. Discuss.: 13 Nov 2012
Abstract. Mercury (Hg) is a neurotoxin that bioaccumulates in the food chain. Mercury is emitted to the atmosphere primarily in its elemental form, which has a long lifetime allowing global transport. It is known that atmospheric oxidation of gaseous elemental mercury (GEM) generates reactive gaseous mercury (RGM) which plays an important role in the atmospheric mercury cycle by enhancing the rate of mercury deposition to ecosystems. However, the primary GEM oxidants, and the chemical composition of RGM are poorly known. Using speciated mercury measurements conducted at the Mt. Bachelor Observatory since 2005 we present two previously unidentified sources of RGM to the free troposphere (FT). Firstly, we observed elevated RGM concentrations, large RGM/GEM-ratios, and anti-correlation between RGM and GEM during Asian long-rang transport events, demonstrating that RGM is formed from GEM by in-situ oxidation in some anthropogenic pollution plumes in the FT. During the Asian pollution events the measured RGM/GEM-enhancement ratios reached peak values, up to ~0.20, which are significantly larger than ratios typically measured (RGM/GEM < 0.03) in the Asian source region. Secondly, we observed very high RGM levels – the highest reported in the FT – in clean air masses that were processed upwind of Mt. Bachelor Observatory over the Pacific Ocean. The high RGM concentrations (up to 700 pg m−3), high RGM/GEM-ratios (up to 1), and very low ozone levels during these events provide observational evidence indicating significant GEM oxidation in the lower FT in some conditions.
Revised: 11 Feb 2013 – Accepted: 21 Feb 2013 – Published: 08 Mar 2013
Timonen, H., Ambrose, J. L., and Jaffe, D. A.: Oxidation of elemental Hg in anthropogenic and marine airmasses, Atmos. Chem. Phys., 13, 2827-2836, doi:10.5194/acp-13-2827-2013, 2013.