Details:

Journal Title:
Atmospheric Chemistry and Physics
Personal Author:
Kaiser, J. ; Skog, K. M. ; Baumann, K. ; Bertman, S. B. ; Brown, S. B. ; ... More +
Kaiser, J. ; Skog, K. M. ; Baumann, K. ; Bertman, S. B. ; Brown, S. B. ; Brune, W. H. ; Crounse, J. D. ; de Gouw, J. A. ; Edgerton, E. S. ; Feiner, P. A. ; Goldstein, A. H. ; Koss, A. ; Misztal, P. K. ; Nguyen, T. B. ; Olson, K. F. ; St. Clair, J. M. ; Teng, A. P. ; Toma, S. ; Wennberg, P. O. ; Wild, R. J. ; Zhang, L. ; Keutsch, F. N. Less -
NOAA Program & Office:
OAR (Oceanic and Atmospheric Research) ; ESRL (Earth System Research Laboratory) ; CIRES (Cooperative Institute for Research in Environmental Sciences) ; CSL (Chemical Sciences Laboratory)
OAR (Oceanic and Atmospheric Research) ; ESRL (Earth System Research Laboratory) ; CIRES (Cooperative Institute for Research in Environmental Sciences) ; CSL (Chemical Sciences Laboratory) Less -
Description:
Measurements of OH reactivity, the inverse lifetime of the OH radical, can provide a top-down estimate of the total amount of reactive carbon in an air mass. Using a comprehensive measurement suite, we examine the measured and modeled OH reactivity above an isoprene-dominated forest in the southeast United States during the 2013 Southern Oxidant and Aerosol Study (SOAS) field campaign. Measured and modeled species account for the vast majority of average daytime reactivity (80-95 %) and a smaller portion of nighttime and early morning reactivity (68-80 %). The largest contribution to total reactivity consistently comes from primary biogenic emissions, with isoprene contributing similar to 60% in the afternoon, and similar to 30-40% at night and monoterpenes contributing similar to 15-25% at night. By comparing total reactivity to the reactivity stemming from isoprene alone, we find that similar to 20% of the discrepancy is temporally related to isoprene reactivity, and an additional constant similar to 1 s(-1) offset accounts for the remaining portion. The model typically overestimates measured OVOC concentrations, indicating that unmeasured oxidation products are unlikely to influence measured OH reactivity. Instead, we suggest that unmeasured primary emissions may influence the OH reactivity at this site.
Source:
Atmospheric Chemistry and Physics, 16(14), 9349-9359.
DOI:
https://doi.org/10.5194/acp-16-9349-2016
Document Type:
Journal Article
Rights Information:
CC BY
Compliance:
Submitted
Main Document Checksum:
[+]
urn:sha256:196e2f8109225df15e2d3648fd2589fa7d8698a5408d194a543b22425ef96d65
Download URL:
https://repository.library.noaa.gov/view/noaa/21654/noaa_21654_DS1.pdf
File Type:

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