Numéro |
J. Phys. IV France
Volume 107, May 2003
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Page(s) | 835 - 838 | |
DOI | https://doi.org/10.1051/jp4:20030428 |
J. Phys. IV France 107 (2003) 835
DOI: 10.1051/jp4:20030428
The role of ocean-atmosphere exchange in the global mercury cycle
R.P. Mason, F.J.G. Laurier, L. Whalin and G.-R. SheuUniversity of Maryland Center for Environmental Science, Chesapeake Biological Laboratory, P.O. Box 38, Solomons, MD 20688, U.S.A.
Abstract
Air-sea exchange of mercury (Hg) is a critical part of the global Hg cycle as it determines the response time of
the biosphere to changes in mercury inputs. The cycling of Hg between the ocean and atmosphere is complex, principally
because of the enhanced oxidation of elemental Hg (Hg
0), and the formation of reactive gaseous Hg (RGHg), in the marine
boundary layer. We estimate that the dry deposition of RGHg to the ocean, which has not been previously considered in
global budgets, is 35% of the total Hg input to the ocean. A further re-evaluation of the global Hg cycle suggests that there
is a net transfer of Hg from the terrestrial environment to the ocean and that the deep ocean Hg concentration is increasing.
Similarly, anthropogenic inputs on land have increased Hg in the Earth's surface layer with accumulation in the terrestrial
environment accounting for nearly 80% of the net input from man's activities. Ultimately, because of the relatively short
residence time of RGHg in the atmosphere, it is the oxidation of Hg
0 over the ocean, rather than RGHg transport from
terrestrial sources, that is primarily contributing to oceanic RGHg deposition.
© EDP Sciences 2003