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dc.contributor.authorZheng, Xiaojian
dc.contributor.authorXi, Baike
dc.contributor.authorDong, Xiquan
dc.contributor.authorLogan, Timothy
dc.contributor.authorWang, Yuan
dc.contributor.authorWu, Peng
dc.date.accessioned2020-09-05T00:04:02Z
dc.date.available2020-09-05T00:04:02Z
dc.date.issued2020-03-24
dc.identifier.citationZheng, X., Xi, B., Dong, X., Logan, T., Wang, Y., & Wu, P. (2020). Investigation of aerosol-cloud interactions under different absorptive aerosol regimes using Atmospheric Radiation Measurement (ARM) southern Great Plains (SGP) ground-based measurements. Atmospheric Chemistry And Physics, 20(6), 3483-3501. doi: 10.5194/acp-20-3483-2020en_US
dc.identifier.issn1680-7316
dc.identifier.doi10.5194/acp-20-3483-2020
dc.identifier.urihttp://hdl.handle.net/10150/642573
dc.description.abstractThe aerosol indirect effect on cloud microphysical and radiative properties is one of the largest uncertainties in climate simulations. In order to investigate the aerosol-cloud interactions, a total of 16 low-level stratus cloud cases under daytime coupled boundary-layer conditions are selected over the southern Great Plains (SGP) region of the United States. The physicochemical properties of aerosols and their impacts on cloud microphysical properties are examined using data collected from the Department of Energy Atmospheric Radiation Measurement (ARM) facility at the SGP site. The aerosol-cloud interaction index (ACI(r)) is used to quantify the aerosol impacts with respect to cloud-droplet effective radius. The mean value of ACI(r) calculated from all selected samples is 0.145 +/- 0.05 and ranges from 0.09 to 0.24 at a range of cloud liquid water paths (LWPs; LWP = 20-300 g m(-2)). The magnitude of ACI(r) decreases with an increasing LWP, which suggests a diminished cloud microphysical response to aerosol loading, presumably due to enhanced condensational growth processes and enlarged particle sizes. The impact of aerosols with different light-absorbing abilities on the sensitivity of cloud microphysical responses is also investigated. In the presence of weak light-absorbing aerosols, the low-level clouds feature a higher number concentration of cloud condensation nuclei (N-CCN) and smaller effective radii (r(e)), while the opposite is true for strong light-absorbing aerosols. Furthermore, the mean activation ratio of aerosols to CCN (N-CCN/N-a) for weakly (strongly) absorbing aerosols is 0.54 (0.45), owing to the aerosol microphysical effects, particularly the different aerosol compositions inferred by their absorptive properties. In terms of the sensitivity of cloud-droplet number concentration (N-d) to N-CCN, the fraction of CCN that converted to cloud droplets (N-d/N-CCN) for the weakly (strongly) absorptive regime is 0.69 (0.54). The measured ACI(r) values in the weakly absorptive regime are relatively higher, indicating that clouds have greater microphysical responses to aerosols, owing to the favorable thermodynamic condition. The reduced ACI(r) values in the strongly absorptive regime are due to the cloud-layer heating effect induced by strong light-absorbing aerosols. Consequently, we expect larger shortwave radiative cooling effects from clouds in the weakly absorptive regime than those in the strongly absorptive regime.en_US
dc.language.isoenen_US
dc.publisherCOPERNICUS GESELLSCHAFT MBHen_US
dc.rightsCopyright © Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License.en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.titleInvestigation of aerosol-cloud interactions under different absorptive aerosol regimes using Atmospheric Radiation Measurement (ARM) southern Great Plains (SGP) ground-based measurementsen_US
dc.typeArticleen_US
dc.contributor.departmentUniv Arizona, Dept Hydrol & Atmospher Scien_US
dc.identifier.journalATMOSPHERIC CHEMISTRY AND PHYSICSen_US
dc.description.noteOpen access journalen_US
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en_US
dc.eprint.versionFinal published versionen_US
dc.source.journaltitleAtmospheric Chemistry and Physics
dc.source.volume20
dc.source.issue6
dc.source.beginpage3483
dc.source.endpage3501
refterms.dateFOA2020-09-05T00:04:02Z


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Copyright © Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License.
Except where otherwise noted, this item's license is described as Copyright © Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License.