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FATE OF MERCURY IN THE ARCTIC Michael Evan ... - COGCI

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Fate of Mercury in the Arctic 24<br />

research team indeed does suggest reactive bromine as one step in the mercury depletion<br />

mechanism and shows that Hg deposition has been decreasing. This researcher however, is not<br />

ready to directly correlate the measured increase of Hg in Arctic biota directly to ozone depletion<br />

events. This is a hypothesis that must be tested with future research.<br />

The work done in this Ph.D. on peat in fact suggests that global Hg deposition has peaked, and<br />

that net deposition is in decline. With an appropriate archive, the high resolution dating technique<br />

developed as a part of this work will provide a useful tool for investigating in detail, deposition to<br />

the Arctic coast since 1960. The chance of finding an appropriate high Arctic archive for this time<br />

period are however, slim, due to freeze thaw destruction of the upper layers of soil.<br />

The post snow melt flux into the marine environment is not yet well described, nor is the total<br />

mass balance for mercury cycling in the Arctic, though it is known that once deposited, the RGM is<br />

methylized, primarily by microbial metabolism, to methylmercury, which has the capacity to collect<br />

in organisms i.e., bioaccumulate, and to concentrate up food chains i.e., biomagnify or<br />

bioconcentrate, especially in the marine food chain.<br />

Atmospheric mercury has been of interest since the 60’s with an overview of mercury in the<br />

atmosphere published by Williston in 1968. Slemr et al., 1985, and Lindqvist and Rodhe (1985)<br />

give one of the first comprehensive distribution, speciation and budget of atmospheric mercury.<br />

Since then, two major reviews of the atmospheric chemistry of mercury have been published:<br />

Schroeder and Munthe, 1998; and Lin and Pekhonen, 1999. These studies are cardinal references<br />

with respect to atmospheric mercury. Lin and Pekhonen establish the lifetime of gaseous elemental<br />

mercury to be about 1 year, given what is known of the atmospheric chemistry of mercury at the<br />

time. The work in this Ph.D. suggests that globally, this may need to be re-evaluated, taking into<br />

consideration the extremely short lifetime of Hg (0) during Arctic polar sunrise.

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