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Volume 12, issue 21
Atmos. Chem. Phys., 12, 10405–10421, 2012
https://doi.org/10.5194/acp-12-10405-2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 12, 10405–10421, 2012
https://doi.org/10.5194/acp-12-10405-2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 07 Nov 2012

Research article | 07 Nov 2012

Wintertime Arctic Ocean sea water properties and primary marine aerosol concentrations

J. Zábori1, R. Krejci1,5, A. M. L. Ekman2,7, E. M. Mårtensson1,3, J. Ström1, G. de Leeuw4,5,6, and E. D. Nilsson1 J. Zábori et al.
  • 1Department of Applied Environmental Science, Stockholm University, 11418 Stockholm, Sweden
  • 2Department of Meteorology, Stockholm University, 11418 Stockholm, Sweden
  • 3Department of Earth Sciences, Uppsala University, 752 36 Uppsala, Sweden
  • 4Meteorological Institute, Climate Change Unit, 00101 Helsinki, Finland
  • 5Department of Physics, University of Helsinki, 00014 Helsinki, Finland
  • 6TNO B&O, NL-3508 TA Utrecht, The Netherlands
  • 7Bert Bolin Centre for Climate Research, Stockholm University, 11418 Stockholm, Sweden

Abstract. Sea spray aerosols are an important part of the climate system through their direct and indirect effects. Due to the diminishing sea ice, the Arctic Ocean is one of the most rapidly changing sea spray aerosol source areas. However, the influence of these changes on primary particle production is not known.

In laboratory experiments we examined the influence of Arctic Ocean water temperature, salinity, and oxygen saturation on primary particle concentration characteristics. Sea water temperature was identified as the most important of these parameters. A strong decrease in sea spray aerosol production with increasing water temperature was observed for water temperatures between −1°C and 9°C. Aerosol number concentrations decreased from at least 1400 cm−3 to 350 cm−3. In general, the aerosol number size distribution exhibited a robust shape with one mode close to dry diameter Dp 0.2 μm with approximately 45% of particles at smaller sizes. Changes in sea water temperature did not result in pronounced change of the shape of the aerosol size distribution, only in the magnitude of the concentrations. Our experiments indicate that changes in aerosol emissions are most likely linked to changes of the physical properties of sea water at low temperatures. The observed strong dependence of sea spray aerosol concentrations on sea water temperature, with a large fraction of the emitted particles in the typical cloud condensation nuclei size range, provide strong arguments for a more careful consideration of this effect in climate models.

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