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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 11, issue 1
Atmos. Chem. Phys., 11, 275–291, 2011
https://doi.org/10.5194/acp-11-275-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 11, 275–291, 2011
https://doi.org/10.5194/acp-11-275-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 14 Jan 2011

Research article | 14 Jan 2011

Evaluation of simulated photochemical partitioning of oxidized nitrogen in the upper troposphere

B. H. Henderson1,2, R. W. Pinder2, J. Crooks2, R. C. Cohen3, W. T. Hutzell2, G. Sarwar2, W. S. Goliff4, W. R. Stockwell5, A. Fahr5, R. Mathur2, A. G. Carlton6, and W. Vizuete1 B. H. Henderson et al.
  • 1Department of Environmental Science and Engineering, University of North Carolina, Chapel Hill, NC, USA
  • 2National Exposure Research Laboratory, US Environmental Protection Agency (USEPA), RTP, NC, USA
  • 3Departments of Chemistry and Earth and Planetary Sciences, University of California, Berkeley, CA, USA
  • 4College of Engineering-CERT, University of California at Riverside, Riverside, CA, USA
  • 5Department of Chemistry, Howard University, Washington, DC, USA
  • 6Department of Environmental Sciences, Rutgers University, New Brunswick, NJ, USA

Abstract. Regional and global chemical transport models underpredict NOx (NO + NO2) in the upper troposphere where it is a precursor to the greenhouse gas ozone. The NOx bias has been shown in model evaluations using aircraft data (Singh et al., 2007) and total column NO2 (molecules cm−2) from satellite observations (Napelenok et al., 2008). The causes of NOx underpredictions have yet to be fully understood due to the interconnected nature of simulated emission, transport, and chemistry processes. Recent observation-based studies, in the upper troposphere, identify chemical rate coefficients as a potential source of error (Olson et al., 2006; Ren et al., 2008). Since typical chemistry evaluation techniques are not available for upper tropospheric conditions, this study develops an evaluation platform from in situ observations, stochastic convection, and deterministic chemistry. We derive a stochastic convection model and optimize it using two simulated datasets of time since convection, one based on meteorology, and the other on chemistry. The chemistry surrogate for time since convection is calculated using seven different chemical mechanisms, all of which predict shorter time since convection than our meteorological analysis. We evaluate chemical simulations by inter-comparison and by pairing results with observations based on NOx:HNO3, a photochemical aging indicator. Inter-comparison reveals individual chemical mechanism biases and recommended updates. Evaluation against observations shows that all chemical mechanisms overpredict NOx removal relative to long-lived methanol and carbon monoxide. All chemical mechanisms underpredict observed NOx by at least 30%, and further evaluation is necessary to refine simulation sensitivities to initial conditions and chemical rate uncertainties.

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