Atmos. Chem. Phys. Discuss., 11, 13381-13424, 2011
www.atmos-chem-phys-discuss.net/11/13381/2011/
doi:10.5194/acpd-11-13381-2011
© Author(s) 2011. 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.
Forest-atmosphere exchange of ozone: sensitivity to very reactive biogenic VOC emissions and implications for in-canopy photochemistry
G. M. Wolfe1,*, J. A. Thornton1, M. McKay2,**, and A. H. Goldstein2
1Department of Atmospheric Sciences, University of Washington, Seattle, WA, USA
2Department of Environmental Science, Policy, and Management, University of California, Berkeley, CA, USA
*now at: Department of Chemistry, University of Wisconsin, Madison, WI, USA
**now at: California Air Resources Board, Sacramento, CA, USA

Abstract. Understanding the fate of ozone within and above forested environments is vital to assessing the anthropogenic impact on ecosystems and air quality at the urban-rural interface. Observed forest-atmosphere exchange of ozone is often much faster than explicable by stomatal uptake alone, suggesting the presence of additional ozone sinks within the canopy. Using the Chemistry of Atmosphere-Forest Exchange (CAFE) model in conjunction with summer noontime observations from the 2007 Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX-2007), we explore the viability and implications of the hypothesis that ozonolysis of very reactive but yet unidentified biogenic volatile organic compounds (BVOC) can influence the forest-atmosphere exchange of ozone. Non-stomatal processes typically generate 67% of the observed ozone flux, but reactions of ozone with measured BVOC, including monoterpenes and sesquiterpenes, can account for only 2% of this flux during the selected timeframe. By incorporating additional emissions and chemistry of a proxy for very reactive VOC (VRVOC) that undergo rapid ozonolysis, we demonstrate that an in-canopy chemical ozone sink of ~2×108 molecules cm−3 s−1 can close the ozone flux budget. Even in such a case, the 65 min chemical lifetime of ozone is much longer than the canopy residence time of ~2 min, highlighting that chemistry can influence reactive trace gas exchange even when it is "slow" relative to vertical mixing. This level of VRVOC ozonolysis could enhance OH and RO2 production by as much as 1 pptv s−1 and substantially alter their respective vertical profiles depending on the actual product yields. Reaction products would also contribute significantly to the oxidized VOC budget and, by extension, secondary organic aerosol mass. Given the potentially significant ramifications of a chemical ozone flux for both in-canopy chemistry and estimates of ozone deposition, future efforts should focus on quantifying both ozone reactivity and non-stomatal (e.g. cuticular) deposition within the forest.

Citation: Wolfe, G. M., Thornton, J. A., McKay, M., and Goldstein, A. H.: Forest-atmosphere exchange of ozone: sensitivity to very reactive biogenic VOC emissions and implications for in-canopy photochemistry, Atmos. Chem. Phys. Discuss., 11, 13381-13424, doi:10.5194/acpd-11-13381-2011, 2011.
 
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