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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 15, issue 6
Atmos. Chem. Phys., 15, 3497–3516, 2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 15, 3497–3516, 2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 31 Mar 2015

Research article | 31 Mar 2015

Aerosol processing and CCN formation of an intense Saharan dust plume during the EUCAARI 2008 campaign

N. Bègue1, P. Tulet1, J. Pelon2, B. Aouizerats3, A. Berger4, and A. Schwarzenboeck5 N. Bègue et al.
  • 1Laboratoire de l'Atmosphère et des Cyclones, UMR 8105 CNRS, University of Réunion Island, Reunion Island, France
  • 2Laboratoire Atmosphère Milieux Observations Spatiales, University of Paris VI, Paris, France
  • 3Faculty of Earth and Life Sciences, VU University Amsterdam, Amsterdam, the Netherlands
  • 4Laboratoire d'Aérologie, University of Paul Sabatier, CNRS, Toulouse, France
  • 5Laboratoire de Météorologie Physique, CNRS, UMR 6016 University Blaise-Pascal, Clermont-Ferrand, France

Abstract. Atmospheric processing and CCN formation of Saharan dust is illustrated through the analysis of a case of dust transport over northern Europe. This spread of dust is investigated by combining satellite, airborne and ground-based observations and the non-hydrostatic meso-scale model Meso-NH. The altitude of the dust plume during its transport to northwestern Europe was assessed using the CALIPSO observations and our model results. The major dust plume was transported toward Mediterranean and European regions between 2 and 5 km above sea level (a.s.l.). This is confirmed by an average particle depolarization ratio equal to 30%. Due to transport, this layer split into two layers over northern Europe, and we analyzed in this paper possible mixing of the European pollution aerosol with dust particles in the lower layer. The simulations have shown that the lower dust layer has interacted with the anthropogenic aerosol mainly over Belgium and the Netherlands. The analyses of numerical simulation results show that mineral dust particles accumulated soluble material through internal mixing over the Netherlands. The value of the CCN0.2 / CN ratio obtained over the Netherlands (~ 70%) is much greater than those observed over the Saharan region. In addition over the Netherlands, the CCN measurement reached 14 000 particles cm−3 at 0.63% supersaturation level on 30 May. Our model results reveal that more than 70% of the CCN concentration observed on 30 May can be explained by the presence of Saharan aged dust. The study reveals that heterogeneous reactions with inorganic salts converted this Saharan mineral dust into compounds that were sufficiently soluble to impact hygroscopic growth and cloud droplet activation over the Netherlands.

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