Monoterpenes are the largest source of summertime organic aerosol in the southeastern United States

Author:

Zhang HaofeiORCID,Yee Lindsay D.,Lee Ben H.ORCID,Curtis Michael P.,Worton David R.,Isaacman-VanWertz Gabriel,Offenberg John H.,Lewandowski Michael,Kleindienst Tadeusz E.,Beaver Melinda R.,Holder Amara L.,Lonneman William A.,Docherty Kenneth S.,Jaoui Mohammed,Pye Havala O. T.,Hu Weiwei,Day Douglas A.,Campuzano-Jost Pedro,Jimenez Jose L.,Guo Hongyu,Weber Rodney J.,de Gouw Joost,Koss Abigail R.,Edgerton Eric S.,Brune William,Mohr Claudia,Lopez-Hilfiker Felipe D.,Lutz Anna,Kreisberg Nathan M.,Spielman Steve R.,Hering Susanne V.,Wilson Kevin R.,Thornton Joel A.,Goldstein Allen H.

Abstract

The chemical complexity of atmospheric organic aerosol (OA) has caused substantial uncertainties in understanding its origins and environmental impacts. Here, we provide constraints on OA origins through compositional characterization with molecular-level details. Our results suggest that secondary OA (SOA) from monoterpene oxidation accounts for approximately half of summertime fine OA in Centreville, AL, a forested area in the southeastern United States influenced by anthropogenic pollution. We find that different chemical processes involving nitrogen oxides, during days and nights, play a central role in determining the mass of monoterpene SOA produced. These findings elucidate the strong anthropogenic–biogenic interaction affecting ambient aerosol in the southeastern United States and point out the importance of reducing anthropogenic emissions, especially under a changing climate, where biogenic emissions will likely keep increasing.

Funder

National Science Foundation

U.S. Department of Energy

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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