Atmos. Chem. Phys. Discuss., 12, 241-282, 2012
www.atmos-chem-phys-discuss.net/12/241/2012/
doi:10.5194/acpd-12-241-2012
© Author(s) 2012. This work is distributed
under the Creative Commons Attribution 3.0 License.
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This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Nitrogen deposition to the United States: distribution, sources, and processes
L. Zhang1,2, D. J. Jacob1,2, E. M. Knipping3, N. Kumar4, J. W. Munger1,2, C. C. Carouge2, A. van Donkelaar5, Y. X. Wang6, and D. Chen7
1Department of Earth and Planetary Sciences, Harvard University, Cambridge, MA, USA
2School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
3Electric Power Research Institute, Washington, DC, USA
4Electric Power Research Institute, Palo Alto, CA, USA
5Department of Physics and Atmospheric Science, Dalhousie University, Halifax, Canada
6Ministry of Education Key Laboratory for Earth System Modeling, Center for Earth System Science, Institute for Global Change Studies, Tsinghua University, Beijing, China
7Department of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA, USA

Abstract. We simulate nitrogen deposition over the US in 2006–2008 by using the GEOS-Chem global chemical transport model at 1/2° × 2/3° horizontal resolution over North America and adjacent oceans. US emissions of NOx and NH3 in the model are 6.7 and 2.9 Tg N a−1 respectively, including a 20% natural contribution for each. Ammonia emissions are a factor of 3 lower in winter than summer, providing a good match to US network observations of NHx (≡NH3 gas + ammonium aerosol) and ammonium wet deposition fluxes. Model comparisons to observed deposition fluxes and surface air concentrations of oxidized nitrogen species (NOy) show overall good agreement but excessive wintertime HNO3 production over the US Midwest and Northeast. This suggests a model overestimate N2O5 hydrolysis in aerosols, and a possible factor is inhibition by aerosol nitrate. Model results indicate a total nitrogen deposition flux of 6.5 Tg N a−1 over the contiguous US, including 4.2 as NOy and 2.3 as NHx. Domestic anthropogenic, foreign anthropogenic, and natural sources contribute respectively 78%, 6%, and 16% of total nitrogen deposition over the contiguous US in the model. The domestic anthropogenic contribution generally exceeds 70% in the east and in populated areas of the west, and is typically 50–70% in remote areas of the west. Total nitrogen deposition in the model exceeds 10 kg N ha−1 a−1 over 35% of the contiguous US.

Citation: Zhang, L., Jacob, D. J., Knipping, E. M., Kumar, N., Munger, J. W., Carouge, C. C., van Donkelaar, A., Wang, Y. X., and Chen, D.: Nitrogen deposition to the United States: distribution, sources, and processes, Atmos. Chem. Phys. Discuss., 12, 241-282, doi:10.5194/acpd-12-241-2012, 2012.
 
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