A numerical model of the cloud-topped planetary boundary-layer: chemistry in marine stratus and the effects on aerosol particles

Authors
Citation
A. Bott, A numerical model of the cloud-topped planetary boundary-layer: chemistry in marine stratus and the effects on aerosol particles, ATMOS ENVIR, 33(12), 1999, pp. 1921-1936
Citations number
40
Categorie Soggetti
Environment/Ecology,"Earth Sciences
Journal title
ATMOSPHERIC ENVIRONMENT
ISSN journal
13522310 → ACNP
Volume
33
Issue
12
Year of publication
1999
Pages
1921 - 1936
Database
ISI
SICI code
1352-2310(199906)33:12<1921:ANMOTC>2.0.ZU;2-5
Abstract
In a numerical study the effect of stratiform clouds on aerosol particles i s investigated. This is done with the one-dimensional chemical microphysica l stratus model CHEMISTRA. In the microphysical part of the model special e mphasis is layed on a detailed description of cloud microphysical processes by means of a joint two-dimensional particle distribution for aerosols and cloud droplets. In the chemical part of the model the particle spectrum is subdivided into three categories referring to unactivated aerosols, small and large cloud droplets. Aqueous-phase chemical reactions are separately t reated in the two droplet size classes. Numerical results show that within the boundary-layer, apart from chemical reactions, the time evolution of chemical reactants is strongly controlled by dynamic and microphysical processes. Due to the turbulent mixing the upt ake of highly water soluble gas-phase compounds by cloud droplets yields a strong concentration decrease not only in cloudy regions but also below the cloud. The highest liquid-phase concentrations of these species are found in small cloud droplets while reactants with low water solubility yield hig her concentrations in big than in small droplets. In the liquid phase the d ominant sulfate source is the nucleation scavenging of aerosols. Sulfate pr oduction by chemical reactions takes place during the day when in the gas p hase SO, is photochemically produced. Hereby the oxidation of sulfur by ozo ne is most important and is mainly observed in small droplets. The uptake o f trace gases by cloud droplets and the sulfate production yield a distinct modification of the physico-chemical microstructure of the cloud condensat ion nuclei. After cloud evaporation a local minimum evolves in the aerosol spectra separating cloud processed from interstitial aerosols. The residual aerosols have an increased mass forming a second maximum in the accumulati on mode of the size distributions. (C) 1999 Published by Elsevier Science L td. All rights reserved.