Abstract
Abstract. Mercury (Hg) contamination is ubiquitous. In order to assess its emissions,
transport, atmospheric reactivity, and deposition pathways, worldwide Hg
monitoring has been implemented over the past 10–20 years, albeit with only
a few stations in the Southern Hemisphere. Consequently, little is known about
the relative contribution of marine and terrestrial Hg sources, which is
important in the context of growing interest in effectiveness evaluation of
Hg mitigation policies. This paper constitutes Part 2 of the study
describing a decade of atmospheric Hg concentrations at Cape Point, South
Africa, i.e. the first long-term (> 10 years) observations in the
Southern Hemisphere. Building on the trend analysis reported in Part 1, here
we combine atmospheric Hg data with a trajectory model to investigate
sources and sinks of Hg at Cape Point. We find that the continent is the
major sink, and the ocean, especially its warm regions (i.e. the Agulhas
Current), is the major source for Hg. Further, we find that mercury concentrations and trends from long-range
transport are independent of the source region (e.g. South America,
Antarctica) and thus indistinguishable. Therefore, by filtering out air
masses from source and sink regions we are able to create a dataset
representing a southern hemispheric background Hg concentrations. Based on
this dataset, we were able to show that the interannual variability in Hg
concentrations at Cape Point is not driven by changes in atmospheric
circulation but rather due to changes in global emissions (gold mining and
biomass burning).
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