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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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Journal ArticleDOI

Atmospheric Hg emissions from preindustrial gold and silver extraction in the Americas: a reevaluation from lake-sediment archives.

TL;DR: Historical changes in atmospheric Hg deposition over the last millennium are evaluated from a suite of lake-sediment cores collected from remote regions of the globe, indicating that atmospheric HG emissions from early mining were modest as compared to more recent industrial-era emissions.
Journal ArticleDOI

Mercury transformation and speciation in flue gases from anthropogenic emission sources: a critical review

TL;DR: In this paper, the authors reviewed the mercury transformation mechanisms and speciation profiles for flue gases formed in and released from coal-fired boilers, nonferrous metal smelters, cement plants, iron and steel plants, waste incinerators, biomass burning and so on.
Journal ArticleDOI

Assessment of Global Mercury Deposition through Litterfall

TL;DR: The quantity of global Hg deposition through litterfall using Monte Carlo simulation of published data sets of litterfall biomass production, tree density, and Hg concentration in litter samples is estimated to be 1180 ± 710 Mg yr(-1), more than two times greater than the estimate by GEOS-Chem.
Journal ArticleDOI

Tracing Sources and Bioaccumulation of Mercury in Fish of Lake Baikal− Angara River Using Hg Isotopic Composition

TL;DR: Hg isotopic composition can be used to track the contribution of anthropogenic sources in fish from a contaminated lake, and it is demonstrated that MIF in fish samples from Bratsk Water Reservoir allow to trace anthropogenic Hg.
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Historical reconstruction of mercury pollution across the Tibetan Plateau using lake sediments.

TL;DR: Current sediment Hg accumulation rate data are in broad agreement with Hg deposition values derived from global models that attribute pollution to sources mainly within southeast Asia, underline the need to understand the local Hg cycle in both regional and global context.
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.
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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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