Atmos. Chem. Phys. Discuss., 12, 16407-16455, 2012
www.atmos-chem-phys-discuss.net/12/16407/2012/
doi:10.5194/acpd-12-16407-2012
© Author(s) 2012. This work is distributed
under the Creative Commons Attribution 3.0 License.
Review Status
This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Thunderstorms and upper troposphere chemistry during the early stages of the 2006 North American Monsoon
M. C. Barth1, J. Lee1, A. Hodzic1, G. Pfister1, W. C. Skamarock1, J. Worden2, J. Wong3, and D. Noone3
1National Center for Atmospheric Research, Boulder, Colorado, USA
2Jet Propulsion Laboratory, Pasadena, California, USA
3Department of Atmospheric and Oceanic Sciences and Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, Colorado, USA

Abstract. In this study, the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) is applied at 4 km horizontal grid spacing to study the meteorology and chemistry over the continental US and Northern Mexico region for the 15 July to 7 August 2006 period, which coincides with the early stages of the North American Monsoon. Evaluation of model results shows that WRF-Chem reasonably represents the large-scale meteorology and strong convective storms, but tends to overestimate weak convection. In the upper troposphere, the WRF-Chem model predicts ozone and carbon monoxide (CO) to within 10–20% of aircraft and sonde measurements. However, the frequency distribution from satellite data indicates that WRF-Chem is lofting too much CO from the boundary layer (BL). Because ozone mixing ratios agree well with these same satellite data, it suggests that chemical production of O3 in the model is overpredicted and compensates for the excess convective lofting of BL air. Analysis of different geographic regions (West Coast, Rocky Mountains, Central Plains, Midwest, and Gulf Coast) reveals that much of the convective transport occurs in the Rocky Mountains, while much of the UT ozone chemical production occurs over the Gulf Coast and Midwest regions where both CO and volatile organic compounds (VOCs) are abundant in the upper troposphere and promote the production of peroxy radicals. In all regions most of the ozone chemical production occurs within 24 h of the air being lofted from the boundary layer. In addition, analysis of the anticyclone and adjacent air indicates that ozone mixing ratios within the anticyclone region associated with the North American Monsoon and just outside the anticyclone are similar. Increases of O3 within the anticyclone are strongly coincident with entrainment of stratospheric air into the anticyclone, but also are from in situ O3 chemical production. In situ O3 production is up to 17% greater within the anticyclone than just outside the anticyclone when the anticyclone is over the Southern US indicating that the enhancement of O3 is most pronounced over regions with abundant VOCs.

Citation: Barth, M. C., Lee, J., Hodzic, A., Pfister, G., Skamarock, W. C., Worden, J., Wong, J., and Noone, D.: Thunderstorms and upper troposphere chemistry during the early stages of the 2006 North American Monsoon, Atmos. Chem. Phys. Discuss., 12, 16407-16455, doi:10.5194/acpd-12-16407-2012, 2012.
 
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