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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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Dissertation

Atmospheric mercury speciation and aerosol properties at Ny-Ålesund

Pan Wang
TL;DR: In this paper, the correlations with meteorological conditions and aerosol number concentrations were analyzed for the correlation with full atmospheric mercury depletion event (AMDE) only appeared at a temperature range of −23 to −12◦C.

Characterization of speciated atmospheric mercury concentration measurements in northern Utah

TL;DR: In this paper, two years of speciated atmospheric mercury data in the Intermountain West are examined for annual, seasonal, and diurnal patterns, as well as influences of precipitation.
Dissertation

Mass-independent Fractionation of Mercury Isotopes in Freshwater Systems

Carla Rose
TL;DR: In this article, the authors demonstrate that reducing both the frequency and intensity of light have a large effect on the expression and magnitude of mass independent fractionation (MIF) in aqueous photo-reduction of Hg(II) and MeHg.

Conditional Sampling for Measuring Mercury Vapor Fluxes

TL;DR: In this paper, the authors adapted conditional sampling (relaxed eddy accumulation), a micrometeorological technique commonly used to measure other trace gas fluxes, to measure surface-air mercury fluxes.
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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