共 89 条
Aerosol loading in the Southeastern United States: reconciling surface and satellite observations
被引:47
作者:

Ford, B.
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h-index: 0
机构:
Colorado State Univ, Dept Atmospher Sci, Ft Collins, CO 80523 USA Colorado State Univ, Dept Atmospher Sci, Ft Collins, CO 80523 USA

Heald, C. L.
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h-index: 0
机构:
MIT, Dept Civil & Environm Engn, Cambridge, MA 02139 USA
MIT, Dept Earth Atmospher & Planetary Sci, Cambridge, MA USA Colorado State Univ, Dept Atmospher Sci, Ft Collins, CO 80523 USA
机构:
[1] Colorado State Univ, Dept Atmospher Sci, Ft Collins, CO 80523 USA
[2] MIT, Dept Civil & Environm Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Earth Atmospher & Planetary Sci, Cambridge, MA USA
基金:
美国国家科学基金会;
关键词:
SECONDARY ORGANIC AEROSOL;
BIOMASS BURNING EMISSIONS;
PARTICULATE MATTER MASS;
SEA-SALT AEROSOLS;
OPTICAL DEPTH;
AIR-QUALITY;
CALIPSO LIDAR;
PM2.5;
US;
PARTICLE;
D O I:
10.5194/acp-13-9269-2013
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
We investigate the seasonality in aerosols over the Southeastern United States using observations from several satellite instruments (MODIS, MISR, CALIOP) and surface network sites (IMPROVE, SEARCH, AERONET). We find that the strong summertime enhancement in satellite-observed aerosol optical depth (AOD) (factor 2-3 enhancement over wintertime AOD) is not present in surface mass concentrations (25-55% summertime enhancement). Goldstein et al. (2009) previously attributed this seasonality in AOD to biogenic organic aerosol; however, surface observations show that organic aerosol only accounts for similar to 35% of fine particulate matter (smaller than 2.5 mu m in aerodynamic diameter, PM2.5) and exhibits similar seasonality to total surface PM2.5. The GEOS-Chem model generally reproduces these surface aerosol measurements, but underrepresents the AOD seasonality observed by satellites. We show that seasonal differences in water uptake cannot sufficiently explain the magnitude of AOD increase. As CALIOP profiles indicate the presence of additional aerosol in the lower troposphere (below 700 hPa), which cannot be explained by vertical mixing, we conclude that the discrepancy is due to a missing source of aerosols above the surface layer in summer.
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页码:9269 / 9283
页数:15
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