Experimental studies on cloud condensation nuclei activation and cloud microphysical properties

Abstract

Atmospheric aerosol particles have the ability to affect climate through cloud interactions and direct scattering and absorption of radiation. These aerosol particles can also affect human health through respiratory system. Aerosol particles are emitted to the atmosphere through direct sources or they can be formed through chemical processes from gas phase precursors. The different atmospheric processes and climate feedbacks of aerosol particles can be studied using process-scale models as well as larger global-scale models. In recent years, it has been found out that certain aerosol species lack information on their thermodynamic properties, causing uncertainties in process-scale modelling as well as global-scale modelling. In addition, transport of aerosols to remote regions, where emissions of aerosol particles are low, is poorly modelled in global-scale models. Furthermore, sources for formed secondary organic aerosol (SOA) include uncertainties in global aerosol-climate models, which causes uncertainty to estimating the radiative forcing (RF). In this thesis, these aspects relating to uncertainties are addressed using process and global-scale modelling. This was done first by evaluating the capability of thermodynamic equilibrium model to reproduce observed hygroscopicity in terms of dimethylamine, sulfuric acid and ammonia containing particles. Second, an in-cloud wet deposition scheme was developed (hereafter referred to as the newly-developed scheme) for global models which use sectional aerosol description. The newlydeveloped wet deposition scheme was tested using ECHAM-HAMMOZ global aerosol-climate model with Sectional Aerosol model for Large-Scale Applications (SALSA) in terms of aerosol vertical distributions and lifetimes. Third, the biotic stress effects to trees over boreal region and their effects to SOA formation, clouds and radiative effects were studied using ECHAM-HAMMOZ with SALSA. The results showed that when the thermodynamic equilibrium model was used to model particles with sizes of the order of couple of tens of nanometers, it was inadequate in estimating the hygroscopic growth of dimethylamine (DMA), sulfuric acid (SA) and ammonia containing particles. Thus, more investigation is needed in terms of thermodynamics of DMA containing systems to properly evaluate its effects to climate. Global aerosol-climate models are very complex and thus making aerosol processes more physically sound can even impair the results. This was seen in the results of the newly-developed, more physical, in-cloud wet deposition scheme as it produced spurious vertical profiles and atmospheric black carbon lifetime when compared to the preexisting scheme. Especially, the atmospheric lifetime of black carbon, in the newly-developed scheme, was 1.6 times longer than in the pre-existing scheme and over 2.6 times longer than has been suggested by experimental studies. Thus, the sensitivity of the newly-developed scheme was tested in terms of internal mixing and emission size distribution of black carbon as well as ageing of aerosol species. These results showed that mixing black carbon with soluble substances produced best results in comparison with the observations as well as atmospheric lifetimes of aerosol species when compared to AEROCOM model means. Lastly, the results studying the biotic stress effects on climate showed that increasing the extent of stress in boreal trees enhanced SOA formation as the emissions of volatile organic compounds (VOCs) were increased. The enhanced SOA formation increased cloud droplet number concentration (CDNC) at cloud top and caused stronger negative RF in both all-sky and clear-sky cases. In the future, aerosol model development should investigate further on the thermodynamic properties of aerosol species, especially with respect to DMA. The wet removal and extent of internal mixing of different aerosol species, especially black carbon, should be further investigated and revised, in global climate models, to properly evaluate the transport of aerosol particles. In addition, sources of atmospheric SOA needs further investigation to properly describe its behaviour in the atmosphere as well as the effects on the climate.