Transport of anthropogenic and biomass burning aerosols from Europe to the Arctic during spring 2008

被引:25
|
作者
Marelle, L. [1 ,2 ,3 ,4 ]
Raut, J. -C. [1 ,2 ,3 ]
Thomas, J. L. [1 ,2 ,3 ]
Law, K. S. [1 ,2 ,3 ]
Quennehen, B. [1 ,2 ,3 ]
Ancellet, G. [1 ,2 ,3 ]
Pelon, J. [1 ,2 ,3 ]
Schwarzenboeck, A. [5 ]
Fast, J. D. [6 ]
机构
[1] Univ Paris 06, Sorbonne Univ, Paris, France
[2] Univ Versailles St Quentin, Paris, France
[3] CNRS, INSU, LATMOS, IPSL, Paris, France
[4] TOTAL SA DS, F-92078 Paris, France
[5] Univ Clermont Ferrand, CNRS, UMR6016, Lab Meteorol Phys, Aubiere, France
[6] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
POLARCAT SUMMER CAMPAIGN; NORTH-AMERICA; AIR-POLLUTION; ATMOSPHERIC AEROSOLS; CLOUD MICROPHYSICS; OPTICAL-PROPERTIES; ORGANIC-COMPOUNDS; BLACK CARBON; MODEL; EMISSIONS;
D O I
10.5194/acp-15-3831-2015
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
During the POLARCAT-France airborne campaign in April 2008, pollution originating from anthropogenic and biomass burning emissions was measured in the European Arctic. We compare these aircraft measurements with simulations using the WRF-Chem model to investigate model representation of aerosols transported from Europe to the Arctic. Modeled PM2.5 is evaluated using European Monitoring and Evaluation Programme (EMEP) measurements in source regions and POLARCAT aircraft measurements in the Scandinavian Arctic. Total PM2.5 agrees well with the measurements, although the model overestimates nitrate and underestimates organic carbon in source regions. Using WRF-Chem in combination with the Lagrangian model FLEXPART-WRF, we find that during the campaign the research aircraft sampled two different types of European plumes: mixed anthropogenic and fire plumes from eastern Europe and Russia transported below 2 km, and anthropogenic plumes from central Europe uplifted by warm conveyor belt circulations to 5-6 km. Both modeled plume types had undergone significant wet scavenging (> 50% PM10) during transport. Modeled aerosol vertical distributions and optical properties below the aircraft are evaluated in the Arctic using airborne lidar measurements. Model results show that the pollution event transported aerosols into the Arctic (> 66.6 degrees N) for a 4-day period. During this 4-day period, biomass burning emissions have the strongest influence on concentrations between 2.5 and 3 km altitudes, while European anthropogenic emissions influence aerosols at both lower (similar to 1.5 km) and higher altitudes (similar to 4.5 km). As a proportion of PM2.5, modeled black carbon and SO4= concentrations are more enhanced near the surface in anthropogenic plumes. The European plumes sampled during the POLARCAT-France campaign were transported over the region of springtime snow cover in northern Scandinavia, where they had a significant local atmospheric warming effect. We find that, during this transport event, the average modeled top-of-atmosphere (TOA) shortwave direct and semi-direct radiative effect (DSRE) north of 60 degrees N over snow and ice-covered surfaces reaches +0.58W m(-2), peaking at +3.3W m(-2) at noon over Scandinavia and Finland.
引用
收藏
页码:3831 / 3850
页数:20
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