Articles | Volume 9, issue 23
Atmos. Chem. Phys., 9, 9249–9261, 2009
https://doi.org/10.5194/acp-9-9249-2009

Special issue: AMMA Tropospheric Chemistry and Aerosols

Atmos. Chem. Phys., 9, 9249–9261, 2009
https://doi.org/10.5194/acp-9-9249-2009

  08 Dec 2009

08 Dec 2009

Aerosol vertical distribution and optical properties over M'Bour (16.96° W; 14.39° N), Senegal from 2006 to 2008

J.-F. Léon1,*, Y. Derimian1, I. Chiapello1, D. Tanré1, T. Podvin1, B. Chatenet2, A. Diallo3, and C. Deroo1 J.-F. Léon et al.
  • 1Laboratoire d'Optique Atmosphérique, CNRS-Université de Lille 1, Villeneuve d'Ascq, France
  • 2Laboratoire Inter-Universitaire des systèmes Atmosphériques, CNRS-Université de Paris 7–12, Créteil, France
  • 3Institut de Recherche pour le Développement, Dakar, Senegal
  • *now at: Laboratoire d'Aérologie, CNRS-Université Paul Sabatier, Toulouse, France

Abstract. We present ground-based measurements of aerosol mass, optical properties and vertical extinction profiles acquired in M'Bour, Senegal (16.96° W; 14.39° N) from January 2006 to September 2008. This place of the world is all year long affected by the export of mineral dust as it moves westward to the north Atlantic ocean. The maximum in the dust activity is observed in summer (June–July), corresponding to a maximum in the aerosol optical thickness (above 0.5) and single scattering albedo (above 0.95). It also corresponds to a maximum in the top altitude of the transported aerosol layer (up to 6 km) and aerosol optical thickness scale height (up to 3.5 km) due to the presence of the Saharan Air Layer located between 2 and 6 km. The late summer shows an additional low level aerosol layer that increases in thickness in autumn. Severe dust storms are also systematically observed in spring (March) but with a lower vertical development and a stronger impact (factor 2 to 3) on the ground-level mass compared to summer. Sporadic events of biomass burning aerosols are observed in winter (January) and particularly in January 2006 when the biomass burning aerosol are advected between 1.5 and 3.5 km high. On average, the seasonal signal in the aerosol optical properties and vertical distribution is very similar from year to year over our 3 year monitoring.

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