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dc.contributor.authorPartridge, DG
dc.contributor.authorVrugt, JA
dc.contributor.authorTunved, P
dc.contributor.authorEkman, AML
dc.contributor.authorGorea, D
dc.contributor.authorSorooshian, A
dc.date.accessioned2018-03-07T14:24:29Z
dc.date.issued2011-07-25
dc.description.abstractNew methodologies are required to probe the sensitivity of parameters describing cloud droplet activation. This paper presents an inverse modeling-based method for exploring cloud-aerosol interactions via response surfaces. The objective function, containing the difference between the measured and model predicted cloud droplet size distribution is studied in a two-dimensional framework, and presented for pseudo-adiabatic cloud parcel model parameters that are pair-wise selected. From this response surface analysis it is shown that the susceptibility of cloud droplet size distribution to variations in different aerosol physiochemical parameters is highly dependent on the aerosol environment and meteorological conditions. In general the cloud droplet size distribution is most susceptible to changes in the updraft velocity. A shift towards an increase in the importance of chemistry for the cloud nucleating ability of particles is shown to exist somewhere between marine average and rural continental aerosol regimes. We also use these response surfaces to explore the feasibility of inverse modeling to determine cloud-aerosol interactions. It is shown that the "cloud-aerosol" inverse problem is particularly difficult to solve due to significant parameter interaction, presence of multiple regions of attraction, numerous local optima, and considerable parameter insensitivity. The identifiability of the model parameters will be dependent on the choice of the objective function. Sensitivity analysis is performed to investigate the location of the information content within the calibration data to confirm that our choice of objective function maximizes information retrieval from the cloud droplet size distribution. Cloud parcel models that employ a moving-centre based calculation of the cloud droplet size distribution pose additional difficulties when applying automatic search algorithms for studying cloud-aerosol interactions. To aid future studies, an increased resolution of the region of the size spectrum associated with droplet activation within cloud parcel models, or further development of fixed-sectional cloud models would be beneficial. Despite these improvements, it is demonstrated that powerful search algorithms remain necessary to efficiently explore the parameter space and successfully solve the cloud-aerosol inverse problem.en_GB
dc.description.sponsorshipWe gratefully acknowledge the financial support of the Bert Bolin Centre for Climate research. We gratefully appreciate G. J. Roelofs, IMAU, Utrecht, the Netherlands, for providing us with the pseudo-adiabatic cloud parcel model used in this study. We gratefully acknowledge Hamish Struthers valuable discussions and his help to improve the readability of the manuscript. Some of the calculations made during the course of this study have been made possible using the LISA cluster from the SARA centre for parallel computing at the University of Amsterdam, the Netherlands. AS acknowledges support from an Office of Naval Research YIP award (N00014-10-1-0811).The authors acknowledge the Swedish Environmental Monitoring Program anen_GB
dc.identifier.citationVol. 11, pp. 7269 - 7287en_GB
dc.identifier.doi10.5194/acp-11-7269-2011
dc.identifier.urihttp://hdl.handle.net/10871/31933
dc.language.isoenen_GB
dc.publisherEuropean Geosciences Union (EGU) / Copernicus Publicationsen_GB
dc.rights© Author(s) 2011. Open access. This work is distributed under the Creative Commons Attribution 3.0 License: https://creativecommons.org/licenses/by/3.0/en_GB
dc.titleInverse modeling of cloud-aerosol interactions – Part 1: Detailed response surface analysisen_GB
dc.typeArticleen_GB
dc.date.available2018-03-07T14:24:29Z
dc.descriptionThis is the final version of the article. Available from EGU via the DOI in this record.en_GB
dc.identifier.journalAtmospheric Chemistry and Physicsen_GB


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