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A Synthesis of Progress and Uncertainties in Attributing the Sources of Mercury in Deposition

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TLDR
It is agreed that the uncertainty is strongly dependent upon scale and that the question as stated is answerable with greater confidence both very near and very far from major point sources, assuming that the “global pool” is a recognizable “source.”
Abstract
A panel of international experts was convened in Madison, Wisconsin, in 2005, as part of the 8th International Conference on Mercury as a Global Pollutant. Our charge was to address the state of science pertinent to source attribution, specifically our key question was: "For a given location, can we ascertain with confidence the relative contributions of local, regional, and global sources, and of natural versus anthropogenic emissions to mercury deposition?" The panel synthesized new research pertinent to this question published over the past decade, with emphasis on four major research topics: long-term anthropogenic change, current emission and deposition trends, chemical transformations and cycling, and modeling and uncertainty. Within each topic, the panel drew a series of conclusions, which are presented in this paper. These conclusions led us to concur that the answer to our question is a "qualified yes," with the qualification being dependent upon the level of uncertainty one is willing to accept. We agreed that the uncertainty is strongly dependent upon scale and that our question as stated is answerable with greater confidence both very near and very far from major point sources, assuming that the "global pool" is a recognizable "source." Many regions of interest from an ecosystem-exposure standpoint lie in between, where source attribution carries the greatest degree of uncertainty.

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Dissertation

Etude paléoenvironnementale du cycle du mercure à travers sa composante élémentaire gazeuse Hg0 : De la réactivité de surface à la reconstruction des atmosphères passées grâce aux archives glaciaires

TL;DR: In this article, a NEEM, Groenland du Nord, nous avons mesure les concentrations en mercure elementaire gazeux dans l'air du neve entre 30 and 76 metres de profondeur, and, grâce a des travaux de modelisation des processus de diffusion, reconstruit les concentrations atmospheriques en Hg° depuis les annees 1950, a une echelle spatiale representative of l'Arctique.
Journal ArticleDOI

Bulk Atmospheric Mercury Fluxes for the Northern Great Plains, USA

TL;DR: In this paper, total atmospheric bulk mercury (Hg) concentration and deposition were measured from August 2008 to November 2010 at nine locations in the Northern Great Plains, USA using passive bulk mercury samplers.

Linking Mining Wastewater Discharge to Methylmercury Production in a Sub-Arctic Peatland

TL;DR: In this article, the authors examined the effects of simulated wastewater (containing 27.2 mg/L SO4) on methylmercury (MeHg) production in pore waters via microbial methylation.

Identification of Atmospheric Mercury Sources and Transport Pathways on Local and Regional Scales.

TL;DR: In this paper, daily event precipitation samples collected in Underhill, VT from 1995-2006 were analyzed for total mercury and results suggest that there were no statistically significant changes in annual mercury wet deposition over time, despite significant emissions reductions in the Northeast United States.
References
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Journal ArticleDOI

The biogeochemical cycling of elemental mercury: Anthropogenic influences☆

TL;DR: A review of the available information on global Hg cycling shows that the atmosphere and surface ocean are in rapid equilibrium; the evasion of Hg0 from the oceans is balanced by the total oceanic deposition of hg(II) from the atmosphere as mentioned in this paper.
Journal ArticleDOI

The Case for Atmospheric Mercury Contamination in Remote Areas

TL;DR: A review of the weaknesses in interpretation and the choice of information that has been used to argue against atmospheric Hg contamination can be found in this paper, where the authors examine the weaknesses of the information used to support the prevailing scientific view that natural geologic sources are the principal contributors of Hg.
Journal ArticleDOI

Global anthropogenic mercury emission inventory for 2000

TL;DR: Wilson et al. as mentioned in this paper presented a new inventory of global emissions of mercury to the atmosphere from anthropogenic sources for the year 2000, showing that the largest emissions of Hg to the global atmosphere occur from combustion of fossil fuels, mainly coal in utility, industrial, and residential boilers.
Journal ArticleDOI

Arctic springtime depletion of mercury

TL;DR: In this paper, the authors show that during the spring (April to early June) of 1995, there were frequent episodic depletions in mercury vapour concentrations in Arctic surface air.
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