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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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The impact of sea ice on the air-sea exchange of mercury in the Arctic Ocean

TL;DR: In this article, the authors examined the air-sea exchange of Hg in the Arctic Ocean using continuous sampling systems during the 2015 U.S. Arctic GEOTRACES cruise from August 9 to October 12.
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How well do environmental archives of atmospheric mercury deposition in the Arctic reproduce rates and trends depicted by atmospheric models and measurements

TL;DR: This review compares the reconstruction of atmospheric Hg deposition rates and historical trends over recent decades in the Arctic, inferred from Hg profiles in natural archives such as lake and marine sediments, peat bogs and glacial firn, against those predicted by three state-of-the-art atmospheric models based on global Hg emission inventories from 1990 onwards.
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Recent advances in understanding and measurement of Hg in the environment: Surface-atmosphere exchange of gaseous elemental mercury (Hg0).

TL;DR: This review focuses on Hg0 flux field observational studies, namely the theory, applications, strengths, and limitations of the various experimental methodologies applied to gauge the exchange flux and decipher active sub-processes, and presents an in-depth review, a comprehensive literature synthesis, and methodological and instrumentation advances for terrestrial and marine H g0 flux studies in recent years.
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Atmospheric mercury measurements onboard the CARIBIC passenger aircraft

TL;DR: The CARIBIC project as discussed by the authors uses a modified Tekran instrument (Tekran Model 2537 A analyser, Tekran Inc., Toronto, Canada) during monthly intercontinental flights between Europe and South and North America, Africa, and Asia.
Journal ArticleDOI

The sea–air exchange of mercury (Hg) in the marine boundary layer of the Augusta basin (southern Italy): Concentrations and evasion flux

TL;DR: The new proposed data set offers a unique and original study on the potential outflow of Hg from the sea-air interface at the basin, and it represents an important step for a better comprehension of the processes occurring in the marine biogeochemical cycle of this element.
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.
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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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