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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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Citations
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Fish respond when the mercury rises

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Effects of hypolimnetic oxygen addition on mercury bioaccumulation in Twin Lakes, Washington, USA.

TL;DR: Assessment of mercury (Hg) in the water column, zooplankton and fish, and related water quality parameters, in Twin Lakes from 2009 to 2012 concluded that lower Hg bioaccumulation in ST compared to NT may be related to bloom dilution in chlorophyll-rich bottom waters, a vertical disconnect between the location of zoopLankton
Journal ArticleDOI

Sensitivity of the global atmospheric cycle of mercury to emissions

TL;DR: In this paper, a systematic investigation of the impact of current uncertainties in Hg emissions from specific source categories on global air Hg concentrations is presented, and the results of a base simulation and three sensitivity simulations conducted with a global chemical transport model for mercury (CTM-Hg) are presented.
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Spatial trend and pollution assessment of total mercury and methylmercury pollution in the Pearl River Delta soil, South China

TL;DR: Both THg and MeHg concentrations were correlated significantly with soil organic matter (OM), but not with soil pH, and two relatively high THg contamination zones located in the northwestern part of the PRD have significantly expanded over the last two decades.
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Evidence for short-range transport of atmospheric mercury to a rural, inland site

TL;DR: In this article, the authors monitored three sites near three sites, including a cement plant (monitored in 2007 and 2008), an urban site and a rural site (both monitored in 2005 and 2008).
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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