Seasonal variation of water-soluble inorganic components in aerosol size-segregated at the puy de Dôme station (1,465 ma.s.l.), France

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Abstract

The size-segregated chemical composition of aerosol particles was investigated during 1 year at the puy de Dôme (1,465 ma.s.l.), France. These measurements aimed to a better understanding of the influence of the air mass origin on the size-segregated chemical composition of the aerosol at an altitude site. Mountain site measurements are important because they are representative of long range transport and useful for model validation. PM 1 mass concentration exhibits a seasonal variability with a summer maximum. The composition of PM 1 did not change significantly in terms of relative contribution of water soluble inorganic ions but is rather variable in term of total mass concentrations. For the PM 10-1, a different seasonal behaviour was found with maxima concentrations in autumn-winter. Aerosols were classified into four different categories according to their air mass origin: marine, marine modified, continental and Mediterranean. The PM 10 aerosol mass at 50 % relative humidity was close to 2.5 μg m -3 in the marine, 4.3 μg m -3 in the marine modified, 10.3 μg m -3 in the continental and 7.7 μg m -3 in the Mediterranean sectors. We noted that the influence of the air mass origin (on the chemical properties) could be seen especially on the PM 10-1. A significant PM 10-1 mode was found in marine, modified marine, and Mediterranean air masses, and PM 1 dominated in the continental air masses samples. As a result, the aerosol chemical composition variability at the puy de Dôme is a function of both the season and air mass type and we provide a chemical composition of the aerosol as a function of each of these environmental factors. © Springer Science+Business Media B.V. 2012.

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Bourcier, L., Sellegri, K., Chausse, P., Pichon, J. M., & Laj, P. (2012). Seasonal variation of water-soluble inorganic components in aerosol size-segregated at the puy de Dôme station (1,465 ma.s.l.), France. Journal of Atmospheric Chemistry, 69(1), 47–66. https://doi.org/10.1007/s10874-012-9229-2

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