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

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decomposition of organic matter<br />

The bulk density of the samples at 47 and 21 cm in the GL profile differ only by a<br />

factor of 1.7x (Fig. 2a), in contrast with the differences in Hg concentrations (15x). We assume<br />

that the bulk density of a given type of peat is a reflection of the extent of its decomposition<br />

(degree of humification). Support for this assumption comes from a detailed spectroscopic<br />

characterisation of organic matter in the Swiss peat bog profile at Etang de la Gruère (Cocozza<br />

et al., 2003). Bulk density, therefore, helps to take into account any changes in metal<br />

concentrations which take place during the decomposition of organic matter. In a recent paper<br />

about Hg accumulation rates in peat cores from Patagonia, Biester et al. (2003) suggested that<br />

bulk density is not an adequate parameter to express changes in peat humification, and that Hg<br />

accumulation rates (calculated as we have described here) should be corrected for humification<br />

to take into account mass loss during decay. However, in the GL peat profile, the difference in<br />

bulk density at 47 versus 21 cm (1.6x) is similar to the difference in Zr concentrations (1.7x).<br />

Zirconium is a conservative element which resides almost exclusively in zircon, and this element<br />

(along with other conservative trace metals) should increase in concentration with increasing<br />

extent of peat decay. In fact, the differences in Zr concentrations are comparable to the<br />

differences in bulk density; taken together these data suggest that the differences in humification<br />

alone cannot explain differences in Hg concentrations by more than a factor of two. As a<br />

consequence of these data and arguments, it is unlikely that physical processes such as organic<br />

matter decomposition can explain the magnitude of the variation in Hg concentrations with depth<br />

in the GL profile.<br />

redox-related processes in the oxic zone<br />

It has been suggested that redox-related transformations of Fe and Mn in marine and<br />

lacustrine sediments may contribute to Hg enrichments in the surface layers of these sediments.<br />

27

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