Detailed comparisons of airborne formaldehyde measurements with box models...

Fried, A., C. A. Cantrell, J. Olson, J. Crawford, P. Weibring, J. Walega, D. Richter, W. Junkermann, R. Volkamer, R. Sinreich, B. Heikes, D. O’Sullivan, D. R. Blake, N. Blake, S. Meinardi, E. Apel, A. Weinheimer, D. Knapp, A. Perring, R. C. Cohen, H. Fuelberg, R. E. Shetter, S. R. Hall, K. Ullmann, W. H. Brune, J. Mao, X. Ren, L. G. Huey, H. Singh, J. W. Hair, D. Riemer, G. S. Diskin, and G. Sachse (2011), Detailed comparisons of airborne formaldehyde measurements with box models during the 2006 INTEX-B and MILAGRO campaigns: potential evidence for significant impacts of unmeasured and multi-generation volatile organic carbon compounds, Atmos. Chem. Phys., 11, 11867-11894, doi:10.5194/acp-11-11867-2011.

Detailed comparisons of airborne CH2 O measurements acquired by tunable diode laser absorption spectroscopy with steady state box model calculations were carried out using data from the 2006 INTEX-B and MILARGO campaign in order to improve our understanding of hydrocarbon oxidation processing. This study includes comparisons over Mexico (including Mexico City), the Gulf of Mexico, parts of the continental United States near the Gulf coast, as well as the more remote Pacific Ocean, and focuses on comparisons in the boundary layer. Select previous comparisons in other campaigns have highlighted some locations in the boundary layer where steady state box models have tended to underpredict CH2 O, suggesting that standard steady state modeling assumptions might be unsuitable under these conditions, and pointing to a possible role for unmeasured hydrocarbons and/or additional primary emission sources of CH2 O. Employing an improved instrument, more detailed measurement-model comparisons with better temporal overlap, up-to-date measurement and model precision estimates, up-to-date rate constants, and additional modeling tools based on both Lagrangian and Master Chemical Mechanism (MCM) runs, we have explained much of the disagreement between observed and predicted CH2 O as resulting from non-steady-state atmospheric conditions in the vicinity of large pollution sources, and have quantified

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Tropospheric Chemistry Program (TCP)