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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 8, issue 2
Atmos. Chem. Phys., 8, 351–368, 2008
© Author(s) 2008. This work is licensed under
the Creative Commons Attribution-NonCommercial-ShareAlike 2.5 License.
Atmos. Chem. Phys., 8, 351–368, 2008
© Author(s) 2008. This work is licensed under
the Creative Commons Attribution-NonCommercial-ShareAlike 2.5 License.

  29 Jan 2008

29 Jan 2008

VOC reactivity in central California: comparing an air quality model to ground-based measurements

A. L. Steiner1, R. C. Cohen2, R. A. Harley3, S. Tonse4, D. B. Millet5, G. W. Schade6, and A. H. Goldstein7 A. L. Steiner et al.
  • 1Department of Atmospheric, Oceanic and Space Sciences, University of Michigan, Ann Arbor, MI, USA
  • 2Department of Chemistry, University of California, Berkeley, CA, USA
  • 3Department of Civil and Environmental Engineering, University of California, Berkeley, CA, USA
  • 4Lawrence Berkeley National Laboratory, Berkeley, CA, USA
  • 5Department of Earth and Planetary Sciences, Harvard University, Cambridge, MA, USA
  • 6Department of Atmospheric Sciences, Texas A{&}M University, College Station, TX, USA
  • 7Department of Environmental Science, Policy and Management, University of California, Berkeley, CA, USA

Abstract. Volatile organic compound (VOC) reactivity in central California is examined using a photochemical air quality model (the Community Multiscale Air Quality model; CMAQ) and ground-based measurements to evaluate the contribution of VOC to photochemical activity. We classify VOC into four categories: anthropogenic, biogenic, aldehyde, and other oxygenated VOC. Anthropogenic and biogenic VOC consist of primary emissions, while aldehydes and other oxygenated VOC include both primary anthropogenic emissions and secondary products from primary VOC oxidation. To evaluate the model treatment of VOC chemistry, we compare calculated and modeled OH and VOC reactivities using the following metrics: 1) cumulative distribution functions of NOx concentration and VOC reactivity (ROH,VOC), 2) the relationship between ROH,VOC and NOx, 3) total OH reactivity (ROH,total) and speciated contributions, and 4) the relationship between speciated ROH,VOC and NOx. We find that the model predicts ROH,total to within 25–40% at three sites representing urban (Sacramento), suburban (Granite Bay) and rural (Blodgett Forest) chemistry. However in the urban area of Fresno, the model under predicts NOx and VOC emissions by a factor of 2–3. At all locations the model is consistent with observations of the relative contributions of total VOC. In urban areas, anthropogenic and biogenic ROH,VOC are predicted fairly well over a range of NOx conditions. In suburban and rural locations, anthropogenic and other oxygenated ROH,VOC relationships are reproduced, but calculated biogenic and aldehyde ROH,VOC are often poorly characterized by measurements, making evaluation of the model with available data unreliable. In central California, 30–50% of the modeled urban VOC reactivity is due to aldehydes and other oxygenated species, and the total oxygenated ROH,VOC is nearly equivalent to anthropogenic VOC reactivity. In rural vegetated regions, biogenic and aldehyde reactivity dominates. This indicates that more attention needs to be paid to the accuracy of models and measurements of both primary emissions of oxygenated VOC and secondary production of oxygenates, especially formaldehyde and other aldehydes, and that a more comprehensive set of oxygenated VOC measurements is required to include all of the important contributions to atmospheric reactivity.

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