Impacts of DMS Emissions and Chemistry on E3SMv2 Simulated Cloud Droplet Numbers and Aerosol Concentrations Over the Southern Ocean

Abstract The accurate representation of cloud droplet number concentration (N d ) is crucial for predicting future climate. However, models often underestimate N d over the Southern Ocean (SO), where natural sources dominate, and aerosols are composed primarily of marine biogenic sulfate and sea spray. This study uses a range of diverse data sets to evaluate and untangle biases in Energy Exascale Earth System Model version 2 (E3SMv2) simulated clouds, aerosols, and sulfur species. The default E3SMv2 underestimates N d over SO by a factor of 2 when compared with observations in 3 km‐resolution simulations. Updating the dimethyl sulfide (DMS) emission and chemistry leads to a better agreement between the model and the observations in N d and boundary layer aerosols, but low biases persist in the free tropospheric aerosol concentrations larger than 70 nm, possibly attributable to insufficient particle growth. Furthermore, updates to DMS emissions and chemistry resulted in reduced vertical DMS concentrations and improved the overall agreement between simulated and observed DMS vertical profiles. Preliminary evaluation also reveals remaining biases in simulated sulfur species, including overestimation in DMS at high latitudes, and in simulated sulfate mass concentration, highlighting the necessity for further efforts to improve the model treatment of relevant processes.

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Publication Details

Journal
Journal of Advances in Modeling Earth Systems
Published
2025-05-01
DOI
https://doi.org/10.1029/2024ms004683
Citations
3
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
3.90

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article

Impacts of DMS Emissions and Chemistry on E3SMv2 Simulated Cloud Droplet Numbers and Aerosol Concentrations Over the Southern Ocean

Meng Huang, Robert W. Wood, Litai Kang, Roger Marchand et al.
3 citations
Journal of Advances in Modeling Earth Systems
Atmospheric chemistry and aerosols
3.90
article

Impacts of DMS Emissions and Chemistry on E3SMv2 Simulated Cloud Droplet Numbers and Aerosol Concentrations Over the Southern Ocean

Meng Huang, Robert W. Wood, Litai Kang, Roger Marchand, Ursula A. Jongebloed, Po‐Lun Ma, Becky Alexander
article en
3 citations

Abstract

Abstract The accurate representation of cloud droplet number concentration (N d ) is crucial for predicting future climate. However, models often underestimate N d over the Southern Ocean (SO), where natural sources dominate, and aerosols are composed primarily of marine biogenic sulfate and sea spray. This study uses a range of diverse data sets to evaluate and untangle biases in Energy Exascale Earth System Model version 2 (E3SMv2) simulated clouds, aerosols, and sulfur species. The default E3SMv2 underestimates N d over SO by a factor of 2 when compared with observations in 3 km‐resolution simulations. Updating the dimethyl sulfide (DMS) emission and chemistry leads to a better agreement between the model and the observations in N d and boundary layer aerosols, but low biases persist in the free tropospheric aerosol concentrations larger than 70 nm, possibly attributable to insufficient particle growth. Furthermore, updates to DMS emissions and chemistry resulted in reduced vertical DMS concentrations and improved the overall agreement between simulated and observed DMS vertical profiles. Preliminary evaluation also reveals remaining biases in simulated sulfur species, including overestimation in DMS at high latitudes, and in simulated sulfate mass concentration, highlighting the necessity for further efforts to improve the model treatment of relevant processes.

Journal of Advances in Modeling Earth SystemsVol. 17(5)
Pacific Northwest National Laboratory (US), University of Washington (US)
National Science Foundation, U.S. Department of Energy, Lawrence Berkeley National Laboratory
Openalex Percentile: Top 7%
Atmospheric chemistry and aerosols
3.90
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