Organic nitrate chemistry and its implications for nitrogen budgets in an...

The core information for this publication's citation.: 
Fisher, J. A., D. J. Jacob, K. R. Travis, P. S. Kim, E. A. Marais, C. Chan, J. D. Crounse, A. Teng, T. B. Nguyen, J. M. St. Clair, R. C. Cohen, P. Romer, B. Nault, P. J. Wooldridge, J. Jimenez-Palacios, P. Campuzano-Jost, D. A. Day, W. Hu, P. Shepson, F. Xiong, D. R. Blake, A. Goldstein, P. K. Misztal, T. F. Hanisco, G. M. Wolfe, T. B. Ryerson, A. Wisthaler, and T. Mikoviny (2016), Organic nitrate chemistry and its implications for nitrogen budgets in an isoprene- and monoterpene-rich atmosphere: constraints from aircraft (SEAC4RS) and ground-based (SOAS) observations in the Southeast US, Atmos. Chem. Phys., 16, 5969-5991, doi:10.5194/acp-16-5969-2016.
Abstract: 

Formation of organic nitrates (RONO2) during oxidation of biogenic volatile organic compounds (BVOCs: isoprene, monoterpenes) is a significant loss pathway for atmospheric nitrogen oxide radicals (NOx), but the chemistry of RONO2 formation and degradation remains uncertain. Here we implement a new BVOC oxidation mechanism (including updated isoprene chemistry, new monoterpene chemistry, and particle uptake of RONO2) in the GEOS-Chem global chemical transport model with  ∼  25  ×  25 km2 resolution over North America. We evaluate the model using aircraft (SEAC4RS) and ground-based (SOAS) observations of NOx, BVOCs, and RONO2 from the Southeast US in summer 2013. The updated simulation successfully reproduces the concentrations of individual gas- and particle-phase RONO2 species measured during the campaigns. Gas-phase isoprene nitrates account for 25–50 % of observed RONO2 in surface air, and we find that another 10 % is contributed by gas-phase monoterpene nitrates. Observations in the free troposphere show an important contribution from long-lived nitrates derived from anthropogenic VOCs. During both campaigns, at least 10 % of observed boundary layer RONO2 were in the particle phase. We find that aerosol uptake followed by hydrolysis to HNO3 accounts for 60 % of simulated gas-phase RONO2 loss in the boundary layer. Other losses are 20 % by photolysis to recycle NOx and 15 % by dry deposition. RONO2 production accounts for 20 % of the net regional NOx sink in the Southeast US in summer, limited by the spatial segregation between BVOC and NOx emissions. This segregation implies that RONO2 production will remain a minor sink for NOx in the Southeast US in the future even as NOx emissions continue to decline.

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Research Program: 
Tropospheric Composition Program (TCP)
Mission: 
SEAC4RS
SOAS