Atmosphere 2014, 5(1), 1-15; doi:10.3390/atmos5010001
Article

Regional Air Quality Model Application of the Aqueous-Phase Photo Reduction of Atmospheric Oxidized Mercury by Dicarboxylic Acids

1 National Exposure Research Laboratory, US Environmental Protection Agency, Research Triangle Park, NC 27711, USA 2 Department of Environmental Sciences, Rutgers University, New Brunswick, NJ 08903, USA
* Author to whom correspondence should be addressed.
Received: 27 October 2013; in revised form: 23 November 2013 / Accepted: 5 December 2013 / Published: 20 December 2013
(This article belongs to the Special Issue Atmospheric Mercury)
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Abstract: In most ecosystems, atmospheric deposition is the primary input of mercury. The total wet deposition of mercury in atmospheric chemistry models is sensitive to parameterization of the aqueous-phase reduction of divalent oxidized mercury (Hg2+). However, most atmospheric chemistry models use a parameterization of the aqueous-phase reduction of Hg2+ that has been shown to be unlikely under normal ambient conditions or use a non mechanistic value derived to optimize wet deposition results. Recent laboratory experiments have shown that Hg2+ can be photochemically reduced to elemental mercury (Hg) in the aqueous-phase by dissolved organic matter and a mechanism and the rate for Hg2+ photochemical reduction by dicarboxylic acids (DCA) has been proposed. For the first time in a regional scale model, the DCA mechanism has been applied. The HO2-Hg2+ reduction mechanism, the proposed DCA reduction mechanism, and no aqueous-phase reduction (NAR) of Hg2+ are evaluated against weekly wet deposition totals, concentrations and precipitation observations from the Mercury Deposition Network (MDN) using the Community Multiscale Air Quality (CMAQ) model version 4.7.1. Regional scale simulations of mercury wet deposition using a DCA reduction mechanism evaluated well against observations, and reduced the bias in model evaluation by at least 13% over the other schemes evaluated, although summertime deposition estimates were still biased by −31.4% against observations. The use of the DCA reduction mechanism physically links Hg2+ reduction to plausible atmospheric processes relevant under typical ambient conditions.
Keywords: mercury deposition; atmospheric mercury

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MDPI and ACS Style

Bash, J.O.; Carlton, A.G.; Hutzell, W.T.; Bullock Jr., O.R. Regional Air Quality Model Application of the Aqueous-Phase Photo Reduction of Atmospheric Oxidized Mercury by Dicarboxylic Acids. Atmosphere 2014, 5, 1-15.

AMA Style

Bash JO, Carlton AG, Hutzell WT, Bullock Jr. OR. Regional Air Quality Model Application of the Aqueous-Phase Photo Reduction of Atmospheric Oxidized Mercury by Dicarboxylic Acids. Atmosphere. 2014; 5(1):1-15.

Chicago/Turabian Style

Bash, Jesse O.; Carlton, Annmarie G.; Hutzell, William T.; Bullock Jr., O. R. 2014. "Regional Air Quality Model Application of the Aqueous-Phase Photo Reduction of Atmospheric Oxidized Mercury by Dicarboxylic Acids." Atmosphere 5, no. 1: 1-15.

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