Journal cover Journal topic
Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
Atmos. Chem. Phys., 10, 9351-9368, 2010
© Author(s) 2010. This work is distributed
under the Creative Commons Attribution 3.0 License.
05 Oct 2010
Long-term trends of black carbon and sulphate aerosol in the Arctic: changes in atmospheric transport and source region emissions
D. Hirdman1, J. F. Burkhart1, H. Sodemann1, S. Eckhardt1, A. Jefferson2,3, P. K. Quinn4, S. Sharma5, J. Ström6, and A. Stohl1
1Norwegian Institute for Air Research (NILU), Norway
2National Oceanic & Atmospheric Administration (NOAA) Earth System Research Laboratory (ESRL) Global Monitoring Division, USA
3Cooperative Institute for Research in Environmental Sciences, University of Colorado, USA
4National Oceanic & Atmospheric Administration (NOAA) Pacific Marine Environmental Lab (PMEL), USA
5Environment Canada, Science and Technology Branch, Climate Research Division, Canada
6Norwegian Polar Institute, Tromsø, Norway

Abstract. As a part of the IPY project POLARCAT (Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, of Climate, Chemistry, Aerosols and Transport) and building on previous work (Hirdman et al., 2010), this paper studies the long-term trends of both atmospheric transport as well as equivalent black carbon (EBC) and sulphate for the three Arctic stations Alert, Barrow and Zeppelin. We find a general downward trend in the measured EBC concentrations at all three stations, with a decrease of −2.1±0.4 ng m−3 yr−1 (for the years 1989–2008) and −1.4±0.8 ng m−3 yr−1 (2002–2009) at Alert and Zeppelin respectively. The decrease at Barrow is, however, not statistically significant. The measured sulphate concentrations show a decreasing trend at Alert and Zeppelin of −15±3 ng m−3 yr−1 (1985–2006) and −1.3±1.2 ng m−3 yr−1 (1990–2008) respectively, while there is no trend detectable at Barrow.

To reveal the contribution of different source regions on these trends, we used a cluster analysis of the output of the Lagrangian particle dispersion model FLEXPART run backward in time from the measurement stations. We have investigated to what extent variations in the atmospheric circulation, expressed as variations in the frequencies of the transport from four source regions with different emission rates, can explain the long-term trends in EBC and sulphate measured at these stations. We find that the long-term trend in the atmospheric circulation can only explain a minor fraction of the overall downward trend seen in the measurements of EBC (0.3–7.2%) and sulphate (0.3–5.3%) at the Arctic stations. The changes in emissions are dominant in explaining the trends. We find that the highest EBC and sulphate concentrations are associated with transport from Northern Eurasia and decreasing emissions in this region drive the downward trends. Northern Eurasia (cluster: NE, WNE and ENE) is the dominant emission source at all Arctic stations for both EBC and sulphate during most seasons. In wintertime, there are indications that the EBC emissions from the eastern parts of Northern Eurasia (ENE cluster) have increased over the last decade.

Citation: Hirdman, D., Burkhart, J. F., Sodemann, H., Eckhardt, S., Jefferson, A., Quinn, P. K., Sharma, S., Ström, J., and Stohl, A.: Long-term trends of black carbon and sulphate aerosol in the Arctic: changes in atmospheric transport and source region emissions, Atmos. Chem. Phys., 10, 9351-9368, doi:10.5194/acp-10-9351-2010, 2010.
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