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We use the ECHAM5-HAMMOZ aerosol-chemistry-climate model to quantify the influence of trace gas–aerosol interactions on the regional and global distributions and optical properties of aerosols for present-day conditions. The model includes fully interactive simulations of gas phase and aerosol chemistry including a comprehensive set of heterogeneous reactions. We find that as a whole, the heterogeneous reactions have only a small effect on the and sulfate burden because of competing effects. The uptake of on dust and sea salt decreases the concentrations while the decrease in OH (that results from the uptake of (, , and ) tends to increase (because of reduced oxidation). The sulfate formed in sea salt aerosols from uptake accounts for 3.7 Tg(S) a−1 (5%) of the total sulfate production. Uptake and subsequent reaction of SO2 on mineral dust contributes to a small formation of sulfate (0.55 Tg(S) a−1,
Julia Schmale, Jakob Boyd Pernov
Athanasios Nenes, Andrea Mario Arangio