A51N-0273
Seasonal differences in aerosol water may reconcile AOT and surface mass measurements in the Southeast U.S.

Friday, 18 December 2015
Poster Hall (Moscone South)
Thien Khoi V Nguyen, Rutgers University New Brunswick, New Brunswick, NJ, United States, Virendra P Ghate, Argonne National Laboratory, Argonne, IL, United States and Ann Marie G Carlton, Rutgers University New Brunswick, Department of Environmental Sciences, New Brunswick, NJ, United States
Abstract:
Summertime aerosol optical thickness (AOT) in the Southeast U.S. is high and sharply enhanced (2-3 times) compared to wintertime AOT. This seasonal pattern is unique to the Southeast U.S. and is of particular interest because temperatures there have not warmed over the past 100 years, contrasting with trends in other U.S. regions. Some investigators hypothesize the Southeast temperature trend is due to secondary organic aerosols (SOA) formed from interactions of biogenic volatile organic compounds (BVOCs) and anthropogenic emissions that create a cooling haze. However, aerosol measurements made at the surface do not exhibit strong seasonal differences in mass or organic fraction to support this hypothesis. In this work, we attempt to reconcile the spatial and temporal distribution of AOT over the U.S. with surface mass measurements by examining trends in particle-phase liquid water, an aerosol constituent that effectively scatters radiation and is removed from aerosols in mass measurements at routine surface monitoring sites. We employ the thermodynamic model ISORROPIA (v2.1) to estimate surface and aloft aerosol water mass concentrations at locations of Interagency Monitoring of Protected Visual Environments (IMPROVE) sites using measured speciated ion mass concentrations and NCEP North American Regional Reanalysis (NARR) meteorological data. Results demonstrate strong seasonal differences in aerosol water in the eastern compared to the western part of the U.S., consistent with geographic patterns in AOT. The highest mean regional seasonal difference from 2000 to 2007 is 5.5 µg m-3 and occurs the Southeast, while the lowest is 0.44 µg m-3 and occurs in the dry Mountain West. Our findings suggest 1) similarity between spatial trends in aerosol water in the U.S. and previously published AOT data from the MODIS-TERRA instrument and 2) similar interannual trends in mean aerosol water and previously published interannual AOT trends from MISR, MODIS-TERRA, MODIS-AQUA, and the Walker Branch AERONET site. These aerosol water results provide a plausible explanation for the geographical and seasonal patterns in AOT, and reconcile AOT with surface mass networks.