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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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Recent palaeolimnological change recorded in Lake Xiaolongwan, northeast China: Climatic versus anthropogenic forcing

TL;DR: In this article, a palaeoecological reconstruction over the past ca. 130 years of Lake Xiaolongwan has been carried out using radiometric methods: 210Pb and 137Cs.
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Use of passive sampling methods and models to understand sources of mercury deposition to high elevation sites in the Western United States.

TL;DR: To understand gaseous oxidized mercury (GOM) sources to the Western US, data was collected with passive samplers for ambient GOM concentrations and dry deposition at 10 sites from the coast of the Pacific Ocean to Great Basin National Park and the potential for use of a new sampling material for GOM was investigated.
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Mercury fluxes over an Australian alpine grassland and observation of nocturnal atmospheric mercury depletion events

TL;DR: In this paper, aerodynamic gradient measurements of the air-surface exchange of gaseous elemental mercury (GEM) were undertaken over a 40'ha alpine grassland in Australia's Snowy Mountains region across a 3-week period during the late rainy season.
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Source attribution for mercury deposition in the contiguous United States: Regional difference and seasonal variation

TL;DR: Total annual mercury deposition caused by foreign anthropogenic emissions is significant compared to that from domestic sources on a national basis, suggesting that a coordinated global emission reduction effort is important for effectively reducing mercury deposition in the 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.
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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.
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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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