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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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OtherDOI

Mercury and methylmercury in reservoirs in Indiana

TL;DR: In this paper, the authors propose a solution to solve the problem of the problem: this paper...,.. ].. ).. )... ;.
Journal ArticleDOI

Mercury wet depositions study at suburban, agriculture and traffic sampling sites.

TL;DR: The relationship of ambient air precipitations with respect to mercury wet depositions at suburban, agriculture and traffic three characteristic sampling sites during the year of 2019 was low to moderate correlated in traffic area, while the relationship between wet deposits and precipitations was insignificant at both suburban and agriculture areas.
Journal ArticleDOI

Mercury distribution in water masses of the South Atlantic Ocean (24°S to 20°S), Brazilian Exclusive Economic Zone.

TL;DR: In this article , the authors provided the first insight into the total mercury (HgT, unfiltered waters) content in the water of the Brazilian Exclusive Economic Zone (BEEZ), within a 24°S to 20°S.
Book ChapterDOI

Modeling of Atmospheric Mercury Deposition in India

TL;DR: In this paper, a global chemistry transport modeling system is applied to characterize the long-range transport and transformations and deposition of the three common forms of atmospheric inorganic mercury, and the modeled wet and dry deposition rates are compared across different areas of India and with other regions.

Patterns of Total Gaseous Mercury Variation Prior to and After Brownfield Remediation in Syracuse, NY

Linghui Meng
TL;DR: In this article, the effect of brownfield removal and site restoration on total gaseous mercury (TGM) concentrations and variations at a brownfield site at the Center of Excellence (CoE) in Syracuse, New York from 2011 to 2016 was investigated.
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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