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Journal ArticleDOI

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

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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Citations
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Antarctic polar plateau snow surface conversion of deposited oxidized mercury to gaseous elemental mercury with fractional long-term burial

TL;DR: The role of the vast Antarctic polar plateau in the global mercury cycle was previously unknown as mentioned in this paper, and for the first time, mercury concentrations in snow and air, combined with vertical flux measurements at the South Pole (November-December 2003 and November 2005) have provided considerable insight into the cycling of this element through the Antarctic environment.
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Atmospheric mercury concentrations and speciation measured from 2004 to 2007 in Reno, Nevada, USA

TL;DR: In this paper, atmospheric elemental, reactive and particulate mercury (Hg) concentrations were measured north of downtown Reno, Nevada, USA from November 2004 to November 2007, and the three-year mean reactive gaseous Hg (RGM) concentration (26pgm −3 ) was higher than values reported for rural sites across the western United States.
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Tracing and quantifying anthropogenic mercury sources in soils of northern france using isotopic signatures.

TL;DR: Findings demonstrate that the contamination signature was preserved in the soils and that the deposition of anthropogenic Hg was predominant compared to reactions leading to isotope fractionation such as biotic and abiotic reduction of Hg(II) and resulting in Hg mobility or evasion from the soils.
Journal ArticleDOI

Environmental mercury contamination of an artisanal zinc smelting area in Weining County, Guizhou, China

TL;DR: A significant Hg pollution to the local environment resulted from the artisanal Zn smelting activities, and total Hg concentration in corn plant tissues increased in the order of grains
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Mercury trends in fish from rivers and lakes in the United States, 1969-2005

TL;DR: It is anticipated that Hg concentrations in fish will respond to changes in atmospheric Hg deposition, however, the magnitude and timing of the response is uncertain.
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.
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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.
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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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