Henze, D. K. and Seinfeld, J. H. and Shindell, D. T. (2009) Inverse modeling and mapping US air quality influences of inorganic PM_(2.5) precursor emissions using the adjoint of GEOS-Chem. Atmospheric Chemistry and Physics, 9 (16). pp. 5877-5903. ISSN 1680-7316. http://resolver.caltech.edu/CaltechAUTHORS:20090923-143137436
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Influences of specific sources of inorganic PM_(2.5) on peak and ambient aerosol concentrations in the US are evaluated using a combination of inverse modeling and sensitivity analysis. First, sulfate and nitrate aerosol measurements from the IMPROVE network are assimilated using the four-dimensional variational (4D-Var) method into the GEOS-Chem chemical transport model in order to constrain emissions estimates in four separate month-long inversions (one per season). Of the precursor emissions, these observations primarily constrain ammonia (NH_3). While the net result is a decrease in estimated US~NH_3 emissions relative to the original inventory, there is considerable variability in adjustments made to NH_3 emissions in different locations, seasons and source sectors, such as focused decreases in the midwest during July, broad decreases throughout the US~in January, increases in eastern coastal areas in April, and an effective redistribution of emissions from natural to anthropogenic sources. Implementing these constrained emissions, the adjoint model is applied to quantify the influences of emissions on representative PM_(2.5) air quality metrics within the US. The resulting sensitivity maps display a wide range of spatial, sectoral and seasonal variability in the susceptibility of the air quality metrics to absolute emissions changes and the effectiveness of incremental emissions controls of specific source sectors. NH_3 emissions near sources of sulfur oxides (SO_x) are estimated to most influence peak inorganic PM_(2.5) levels in the East; thus, the most effective controls of NH_3 emissions are often disjoint from locations of peak NH_3 emissions. Controls of emissions from industrial sectors of SO_x and NO_x are estimated to be more effective than surface emissions, and changes to NH_3 emissions in regions dominated by natural sources are disproportionately more effective than regions dominated by anthropogenic sources. NOx controls are most effective in northern states in October; in January, SO_x controls may be counterproductive. When considering ambient inorganic PM_(2.5) concentrations, intercontinental influences are small, though transboundary influences within North America are significant, with SO_x emissions from surface sources in Mexico contributing almost a fourth of the total influence from this sector.
|Additional Information:||© Author(s) 2009. This work is distributed under the Creative Commons Attribution 3.0 License. Received: 1 July 2008 – Published in Atmos. Chem. Phys. Discuss.: 8 August 2008. Revised: 10 August 2009 – Accepted: 10 August 2009 – Published: 19 August 2009. This work was supported by US Environmental Protection Agency, grant R832158, a Columbia University Earth Institute Postdoctoral Fellowship, and NASA’s Atmospheric Chemistry Modeling and Analysis Program. Thanks are also given to supercomputing resources at NCCS and JPL.|
|Official Citation:||Henze, D. K., Seinfeld, J. H., and Shindell, D. T.: Inverse modeling and mapping US air quality influences of inorganic PM2.5 precursor emissions using the adjoint of GEOS-Chem, Atmos. Chem. Phys., 9, 5877-5903, 2009.|
|Usage Policy:||This work is distributed under the Creative Commons Attribution 3.0 License.|
|Deposited By:||George Porter|
|Deposited On:||24 Sep 2009 22:36|
|Last Modified:||26 Dec 2012 11:25|
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