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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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Sensitivity analysis of an updated bidirectional air–surface exchange model for elemental mercury vapor

TL;DR: In this paper, a box model for estimating bidirectional air-surface exchange of gaseous elemental mercury (Hg0) has been updated based on the latest understanding of the resistance scheme of atmosphere-biosphere interface transfer.
Journal ArticleDOI

Geochemical legacies and the future health of cities: A tale of two neurotoxins in urban soils

TL;DR: There is a paradigmatic shift from reaction to and remediation of acute exposures towards a more nuanced understanding of the dynamic cycling of persistent environmental contaminants with resultant widespread and chronic exposure of inner-city dwellers, leading to chronic toxic illness and disability at substantial human and social cost.
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Trade-Induced Atmospheric Mercury Deposition over China and Implications for Demand-Side Controls

TL;DR: The effect of China's interregional trade on atmospheric Hg deposition over China is investigated using an atmospheric transport model and multiregional input-output analysis, suggesting a need for joint mitigation to mitigate China's Hg pollution.
Journal ArticleDOI

Isotopic Composition of Gaseous Elemental Mercury in the Marine Boundary Layer of East China Sea

TL;DR: In this article, the authors measured the concentrations of gaseous elemental mercury (GEM), particulate bound mercury (PbM), and the GEM isotopic composition in the marine boundary layer of East China Sea from October 2013 to January 2014, and found that most events of elevated GEM are associated with the outflow of Hg emissions in mainland China.
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.
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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