1Particle Chemistry Department, Max Planck Institute for Chemistry, Hahn-Meitner-Weg 1, 55128 Mainz, Germany
2Department of Earth Sciences, Indian Institute of Science Education and Research Mohali, Sector 81, SAS Nagar, Manauli PO 140306, India
3Leibniz-Institute for Tropospheric Research (TROPOS), Permoserstrasse 15, 04318 Leipzig, Germany
4Department of Atmospheric Science, Colorado State University, Fort Collins, CO 80523, USA
5Institute de recherches sur la catalyse et l'environnement de Lyon (IRCE Lyon), University of Lyon, 69100 Villeurbanne, France
6Earth System Science Research Centre, Institute for Geosciences, University of Mainz, Becherweg 21, 55128 Mainz, Germany
*now at: Laboratory for Air Pollution and Environmental Technology, EMPA, Überlandstrasse 129, 8600 Dübendorf, Switzerland
**now at: Department of Earth and Planetary Science, ARC Centre for Core to Crust Fluid Systems, Building E7A, Macquarie University, North Ryde, NSW 2109, Australia
***now at: Department of Environmental Sciences, Hankuk University of Foreign Studies, Yongin, South Korea
Received: 03 Dec 2013 – Published in Atmos. Chem. Phys. Discuss.: 28 Jan 2014
Abstract. In-cloud production of sulfate modifies aerosol size distribution, with important implications for the magnitude of indirect and direct aerosol cooling and the impact of SO2 emissions on the environment. We investigate which sulfate sources dominate the in-cloud addition of sulfate to different particle classes as an air parcel passes through an orographic cloud. Sulfate aerosol, SO2 and H2SO4 were collected upwind, in-cloud and downwind of an orographic cloud for three cloud measurement events during the Hill Cap Cloud Thuringia campaign in autumn 2010 (HCCT-2010). Combined SEM and NanoSIMS analysis of single particles allowed the δ34S of particulate sulfate to be resolved for particle size and type.
Revised: 28 Mar 2014 – Accepted: 07 Apr 2014 – Published: 28 Apr 2014
The most important in-cloud SO2 oxidation pathway at HCCT-2010 was aqueous oxidation catalysed by transition metal ions (TMI catalysis), which was shown with single particle isotope analyses to occur primarily in cloud droplets nucleated on coarse mineral dust. In contrast, direct uptake of H2SO4 (g) and ultrafine particulate were the most important sources modifying fine mineral dust, increasing its hygroscopicity and facilitating activation. Sulfate addition to "mixed" particles (secondary organic and inorganic aerosol) and coated soot was dominated by in-cloud aqueous SO2 oxidation by H2O2 and direct uptake of H2SO4 (g) and ultrafine particle sulfate, depending on particle size mode and time of day. These results provide new insight into in-cloud sulfate production mechanisms, and show the importance of single particle measurements and models to accurately assess the environmental effects of cloud processing.
Citation: Harris, E., Sinha, B., van Pinxteren, D., Schneider, J., Poulain, L., Collett, J., D'Anna, B., Fahlbusch, B., Foley, S., Fomba, K. W., George, C., Gnauk, T., Henning, S., Lee, T., Mertes, S., Roth, A., Stratmann, F., Borrmann, S., Hoppe, P., and Herrmann, H.: In-cloud sulfate addition to single particles resolved with sulfur isotope analysis during HCCT-2010, Atmos. Chem. Phys., 14, 4219-4235, doi:10.5194/acp-14-4219-2014, 2014.