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

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

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Fate of Mercury in the Arctic 20<br />

Given the amount of RGM measured in this study, when extrapolated to the Arctic by the<br />

Danish Eulerian Hemispheric Model, the amount of mercury deposited to the Arctic doubles to<br />

about 200 tons per year, or approximately 4.5% of the global total emissions as a result of the<br />

springtime arctic mercury depletion episode (Skov et al., 2003, Appendix C).<br />

It is hypothesized that in the Arctic, this mercury is thereafter released at snowmelt into an<br />

ecosystem starving for nourishment. It is therefore subject to immediate uptake into the marine food<br />

web with subsequent methylation and bioaccumulation to follow.<br />

Little is known of the magnitude of the transformation and subsequent re-emission of mercury<br />

as Hg (0). Reactive species, operationally known as reactive gaseous mercury (RGM) identified as<br />

HgXY are typically HgCl2 from power plants, in industrial areas, as well as total particulate<br />

mercury (TPM) will eventually deposit via dry or wet deposition. The true product or products,<br />

HgXY, have not yet been identified in the Arctic region. A summary of what is known with respect<br />

to Arctic atmospheric mercury, as well as identified needs and data gaps are found in Schroeder et<br />

al., 2003.<br />

2.3 Mercury recorded in environmental archives<br />

Post depositional processes for Hg or HgXY include biological or physical fixation, i.e.<br />

adsorption, and subsequent diagenesis, to include chemical oxidation or reduction and subsequent<br />

reemission of at least a portion of the mercury. Gaseous reemission, especially in tropical areas, or<br />

physical reemission through aeolian transport, adsorbed to particles. Reemission of mercury is one<br />

of the ongoing research areas and is very relevant to the global cycle.<br />

Due to a portion of the deposited mercury being reemitted, it must be understood that<br />

environmental archives of mercury represent a net record of accumulation, one that has been subject<br />

to the deposited mercury being subjected to physical and chemical processes that affect the overall<br />

amount of mercury that remains in the archive from year to year. Depending on the archive, and the

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