Aerosol hygroscopicity over the southeast Atlantic Ocean during the biomass burning season - Part 1: From the perspective of scattering enhancement

Lu Zhang, Michal Segal-Rozenhaimer*, Haochi Che*, Caroline Dang, Junying Sun, Ye Kuang, Paola Formenti, Steven G. Howell

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Aerosol hygroscopicity plays a vital role in aerosol radiative forcing. One key parameter describing hygroscopicity is the scattering enhancement factor, f(RH), defined as the ratio of the scattering coefficient at humidified relative humidity (RH) to its dry value. Here, we utilize the f(80 %) from ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) 2016 and 2018 airborne measurements to investigate the hygroscopicity of aerosols, its vertical distribution, its relationship with chemical composition, and its sensitivity to organic aerosol (OA) hygroscopicity over the southeast Atlantic (SEA) Ocean during the biomass burning (BB) season. We found that aerosol hygroscopicity remains steady above 2 km, with a mean f(80 %) of 1.40 ± 0.17. Below 2 km, aerosol hygroscopicity increases with decreasing altitude, with a mean f(80 %) of 1.51 ± 0.22, consistent with higher values of BB aerosol hygroscopicity found in the literature. The hygroscopicity parameter of OA (κOA) is retrieved from the Mie model with a mean value of 0.11 ± 0.08, which is in the middle to upper range compared to the literature. Higher OA hygroscopicity is related to aerosols that are more aged, oxidized, and present at lower altitudes. The enhanced biomass burning aerosol (BBA) hygroscopicity at lower altitudes is mainly due to a lower OA fraction, increased sulfate fraction, and greater κOA at lower altitudes. We propose a parameterization that quantifies f(RH) with chemical composition and κOA based on Mie simulation of internally mixed OA-(NH4)2SO4-BC mixtures. The good agreement between the predictions and the ORACLES measurements implies that the aerosols in the SEA during the BB season can be largely represented by the OA-(NH4)2SO4-BC internal mixture with respect to the f(RH) prediction. The sensitivity of f(RH) to κOA indicates that applying a constant κOA is only suitable when the OA fraction is low and κOA shows limited variation. However, in situations deviating these two criteria, κOA can notably impact scattering coefficients and aerosol radiative effect; therefore, accounting for κOA variability is recommended.

Original languageEnglish
Pages (from-to)13849-13864
Number of pages16
JournalAtmospheric Chemistry and Physics
Volume24
Issue number23
DOIs
StatePublished - 13 Dec 2024

Funding

FundersFunder number
National Aeronautics and Space Administration
Centre National d’Etudes Spatiales
FP7/2014
RadiatiOn and CLOuds
Tel Aviv University
French National Agency for Space Studies
National Research Foundation
U.S. Department of EnergyDE-SC0020084
Agence Nationale de la RechercheANR-15-CE01-0014-01
European Union's Seventh Framework Programme312609
National Research Foundation of KoreaUID 105958

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