Abstract

Abstract. Lidar and in situ observations performed during the Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, Climate, Chemistry, Aerosols and Transport (POLARCAT) campaign are reported here in terms of statistics to characterize aerosol properties over northern Europe using daily airborne measurements conducted between Svalbard and Scandinavia from 30 March to 11 April 2008. It is shown that during this period a rather large number of aerosol layers was observed in the troposphere, with a backscatter ratio at 532 nm of 1.2 (1.5 below 2 km, 1.2 between 5 and 7 km and a minimum in between). Their sources were identified using multispectral backscatter and depolarization airborne lidar measurements after careful calibration analysis. Transport analysis and comparisons between in situ and airborne lidar observations are also provided to assess the quality of this identification. Comparison with level 1 backscatter observations of the spaceborne Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) were carried out to adjust CALIOP multispectral observations to airborne observations on a statistical basis. Recalibration for CALIOP daytime 1064 nm signals leads to a decrease of their values by about 30%, possibly related to the use of the version 3.0 calibration procedure. No recalibration is made at 532 nm even though 532 nm scattering ratios appear to be biased low (−8%) because there are also significant differences in air mass sampling between airborne and CALIOP observations. Recalibration of the 1064 nm signal or correction of −5% negative bias in the 532 nm signal both could improve the CALIOP aerosol colour ratio expected for this campaign. The first hypothesis was retained in this work. Regional analyses in the European Arctic performed as a test emphasize the potential of the CALIOP spaceborne lidar for further monitoring in-depth properties of the aerosol layers over Arctic using infrared and depolarization observations. The CALIOP April 2008 global distribution of the aerosol backscatter reveal two regions with large backscatter below 2 km: the northern Atlantic between Greenland and Norway, and northern Siberia. The aerosol colour ratio increases between the source regions and the observations at latitudes above 70° N are consistent with a growth of the aerosol size once transported to the Arctic. The distribution of the aerosol optical properties in the mid-troposphere supports the known main transport pathways between the mid-latitudes and the Arctic.

Highlights

  • It is recognized that long-range transport of anthropogenic and biomass burning emissions from lower latitudes is the primary source of aerosol in the Arctic (Quinn et al, 2008; Warneke et al, 2010)

  • Considering the large uncertainty in the weak aerosol layers detected in the AL2 product over the Arctic, averaging of the level 1 (L1) version 3.01 Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) data is used in this paper to analyse the 45 Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) tracks available in the aircraft campaign domain

  • To verify that large CRa for uncorrected IR data is not related to a bias introduced by the averaging of many profiles before the calculation of the colour ratio, we have looked at the R532(z) versus R1064(z) scatter plot using all the 80 km resolution CALIOP-filtered data for the altitude ranges, 0– 7 and 13–15 km

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Summary

Introduction

It is recognized that long-range transport of anthropogenic and biomass burning emissions from lower latitudes is the primary source of aerosol in the Arctic (Quinn et al, 2008; Warneke et al, 2010). Frequent haze and cloud layers in the winter–spring period contribute to surface heating by their infrared emission (Garrett and Zhao, 2006). The relative influence of the different mid-latitude aerosol sources was initially discussed by Rahn (1981) who concluded that the Eurasian transport pathway is important using meteorological considerations and observations. Law and Stohl (2007) stressed the seasonal change of air pollution transport into the Arctic with a faster winter circulation, implying a stronger influence of the southerly sources in the mid- and upper troposphere. G. Ancellet et al.: Transport of aerosol to the Arctic: analysis of CALIOP and aircraft data

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