Aircraft Measurement of Isoprene-derived Organic Aerosol during the Southeast Nexus (SENEX) Campaign Using an Aerosol Mass Spectrometer

Lu Xu1, Ann Middlebrook2, Jin Liao3, Andre Welti4, Hongyu Guo5, Jack J Lin6, Aikaterini Bougiatioti7, Rodney J Weber8, Athanasios Nenes9, John S Holloway10, Jessica Gilman2, Brian M Lerner11, Martin Graus12, Carsten Warneke3, Michael Trainer13, Joost A de Gouw14 and Nga Lee Ng15, (1)Georgia Institute of Technology, School of Chemical and Biomolecular Engineering, Atlanta, GA, United States, (2)NOAA Chemical Sciences Laboratory, Boulder, United States, (3)NOAA Boulder, Boulder, CO, United States, (4)ETH Swiss Federal Institute of Technology Zurich, Zurich, Switzerland, (5)Georgia Institute of Technology, Earth and Atmospheric Sciences, Atlanta, GA, United States, (6)Georgia Tech, Atlanta, GA, United States, (7)National Technical University of Athens (NTUA), Marousi Athens, Greece, (8)Georgia Inst Technology, Atlanta, GA, United States, (9)Ecole Polytechnique Federale de Lausanne, School of Architecture, Civil and Environmental Engineering (ENAC), Laboratory of Atmospheric Processes and their Impacts (LAPI), Lausanne, Switzerland, (10)CIRES, Boulder, CO, United States, (11)Aerodyne Research, Inc., Billerica, MA, United States, (12)Cooperative Institute for Research in Environmental Sciences, Boulder, CO, United States, (13)NOAA Earth System Research Lab, Boulder, CO, United States, (14)University of Colorado Boulder, Department of Chemistry, Boulder, United States, (15)Georgia Institute of Technology Main Campus, School of Chemical and Biomolecular Engineering, School of Earth and Atmospheric Sciences, School of Civil and Environmental Engineering, Atlanta, United States
Abstract:
Isoprene is an important precursor for secondary organic aerosol (SOA) formation due to its large global emissions and high reactivity. Recent studies have found that isoprene SOA formation via the uptake of isoprene epoxydiol (IEPOX) under low NOx conditions appears to be largely affected by anthropogenic emissions and are not well understood. Here we investigate the effects of anthropogenic emissions on isoprene SOA formation through airborne measurements above the southeastern US, which is an ideal location for this study since this area is characterized by high emissions of both anthropogenic and isoprene sources. An Aerodyne Aerosol Mass Spectrometer (AMS) was deployed aboard the NOAA WP-3D aircraft during the Southeast Nexus (SENEX) field campaign to characterize the non-refractory chemical composition of submicron aerosol. Positive Matrix Factorization (PMF) analysis was performed on the organic aerosol (OA) mass spectra to identify patterns of organic components and various OA factors were resolved. Low-volatility Oxygenated Organic Aerosol (LV-OOA) constituted a major fraction of OA. Isoprene-derived OA was also identified in certain flights and correlated well with sulfate. This result is consistent with our recent finding from ground-based measurements in Centreville during the Southern Oxidant and Aerosol Study (SOAS) field campaign that isoprene-derived OA is directly modulated by the abundance of sulfate. The vertical distribution of isoprene-derived OA will be discussed along with the timescale of the effect of sulfate on isoprene OA formation.