Global Impacts of Marine Methanethiol Emissions and Chemistry in the Atmosphere

Oceanic emissions of dimethyl sulfide (DMS) have long been known to influence aerosol particle composition, cloud condensation nuclei (CCN) concentration, and Earth's radiative budget. However, the impact of oceanic emissions of methanethiol (MeSH), a sulfur compound produced by the same oceanic precursor as DMS, has been relatively less explored. The gas-phase oxidation of MeSH has a higher effective yield of SO<sub>2</sub> and a shorter oxidative lifetime compared to DMS, highlighting the relevance of this pathway for the modeled representation of particle formation, growth, and CCN abundance in the marine atmosphere. Here, we use the global chemical transport model GEOS-Chem to explore possible scenarios representative of specific environmental conditions and MeSH emission schemes based on previous experimental studies. We further implement and test previously reported chemical mechanisms for MeSH oxidation, along with additional improvements, highlighting key uncertainties and sensitivities for regional and global sulfur budgets. We place our results in the context of recent modeling updates to DMS chemistry and cloud processing, which further impact SO<sub>2</sub> production in the marine atmosphere in parallel with MeSH oxidation. Within the overall marine sulfur budget, our findings highlight that MeSH plays a significant role in SO<sub>2</sub> production in the marine atmosphere, contributing to regional surface layer concentration increases of up to 40-60%. These results point to the importance of MeSH for efforts aimed at improving the modeled representation of sulfur spatiotemporal patterns relevant to air quality predictions and climate impact assessments.

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Publication Details

Journal
Environmental Science & Technology
Published
2025-09-18
DOI
https://doi.org/10.1021/acs.est.5c02019
Citations
1
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
1.30
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article

Global Impacts of Marine Methanethiol Emissions and Chemistry in the Atmosphere

William C. Porter, Delaney B. Kilgour, Timothy H. Bertram, Andrew W. Rollins et al.
1 citations
Environmental Science & Technology
Atmospheric chemistry and aerosols
1.30
article

Global Impacts of Marine Methanethiol Emissions and Chemistry in the Atmosphere

William C. Porter, Delaney B. Kilgour, Timothy H. Bertram, Andrew W. Rollins, Linia Tashmim
article en
1 citations

Abstract

Oceanic emissions of dimethyl sulfide (DMS) have long been known to influence aerosol particle composition, cloud condensation nuclei (CCN) concentration, and Earth's radiative budget. However, the impact of oceanic emissions of methanethiol (MeSH), a sulfur compound produced by the same oceanic precursor as DMS, has been relatively less explored. The gas-phase oxidation of MeSH has a higher effective yield of SO<sub>2</sub> and a shorter oxidative lifetime compared to DMS, highlighting the relevance of this pathway for the modeled representation of particle formation, growth, and CCN abundance in the marine atmosphere. Here, we use the global chemical transport model GEOS-Chem to explore possible scenarios representative of specific environmental conditions and MeSH emission schemes based on previous experimental studies. We further implement and test previously reported chemical mechanisms for MeSH oxidation, along with additional improvements, highlighting key uncertainties and sensitivities for regional and global sulfur budgets. We place our results in the context of recent modeling updates to DMS chemistry and cloud processing, which further impact SO<sub>2</sub> production in the marine atmosphere in parallel with MeSH oxidation. Within the overall marine sulfur budget, our findings highlight that MeSH plays a significant role in SO<sub>2</sub> production in the marine atmosphere, contributing to regional surface layer concentration increases of up to 40-60%. These results point to the importance of MeSH for efforts aimed at improving the modeled representation of sulfur spatiotemporal patterns relevant to air quality predictions and climate impact assessments.

Environmental Science & TechnologyVol. 59(38)
University of California, Riverside (US), University of Wisconsin–Madison (US), University of California System (US), NOAA Chemical Sciences Laboratory (US), NOAA Earth System Research Laboratory (US)
Openalex Percentile: Top 18%
Atmospheric chemistry and aerosols
1.30
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