Sources and Fate of Reactive Carbon over North America
Abstract
We apply a high-resolution chemical transport model (GEOS-Chem CTM at 0.25°×0.3125°) to generate, a comprehensive gas-phase reactive carbon budget over North America. Based on state-of-science source inventories and known chemistry, we find in the model that biogenic sources dominate the overall reactive carbon budget, with 49, 15, 4, and 39 TgC, respectively, introduced to the North American atmosphere from the biosphere, anthropogenic sources, fires, and from methane oxidation in 2013. Biogenic and anthropogenic non-methane volatile organic compounds contribute 60% and 10%, respectively, to the total OH reactivity over the Southeast US, along with other contributions from methane and inorganics. Oxidation to CO and CO2 then represents the overwhelming fate of that reactive carbon, with 65, 15, 7 and 5 TgC, respectively, oxidized to produce CO/CO2, dry deposited, wet deposited and transported (net) out of North America. We confront this simulation with an ensemble of recent airborne measurements over North America (SEAC4RS, SENEX, DISCOVER-AQ, DC3) and interpret the model-measurement comparisons in terms of their implications for current understanding of atmospheric reactive carbon and the processes driving its distribution.
- Publication:
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AGU Fall Meeting Abstracts
- Pub Date:
- December 2016
- Bibcode:
- 2016AGUFM.A33H0367C
- Keywords:
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- 0305 Aerosols and particles;
- ATMOSPHERIC COMPOSITION AND STRUCTUREDE: 0317 Chemical kinetic and photochemical properties;
- ATMOSPHERIC COMPOSITION AND STRUCTUREDE: 0322 Constituent sources and sinks;
- ATMOSPHERIC COMPOSITION AND STRUCTUREDE: 0365 Troposphere: composition and chemistry;
- ATMOSPHERIC COMPOSITION AND STRUCTURE