Methanethiol Abundance and Oxidation in a Polluted Marine Atmosphere

Abstract Biological activity in the surface ocean leads to emissions of methanethiol (MeSH) and dimethyl sulfide (DMS). Measurements of MeSH in the marine atmosphere are sparse and the impact of NO x pollution on MeSH oxidation remains unexplored. We present measurements of MeSH and DMS at a coastal site with NO x up to 24.3 ppb in the United Kingdom during May and June. Winds coming from the seaward (northerly) direction showed a median (25th quantiles) MeSH mixing ratio of 15.7 (7.9–26.9) ppt. The measurements reveal significantly lower MeSH during daytime. Atmospheric box model calculations suggest that ∼25% of the MeSH oxidation is initiated by NO 3 at this site and that NO x pollution can reduce the SO 2 yield from MeSH. This work is further evidence for the prevalence of MeSH and illustrates the impact of NO x pollution on MeSH oxidation with associated implications for its role in aerosol‐cloud processes, and climate.

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Publication Details

Journal
Geophysical Research Letters
Published
2025-04-28
DOI
https://doi.org/10.1029/2025gl114929
Citations
2
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
2.60

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article

Methanethiol Abundance and Oxidation in a Polluted Marine Atmosphere

Grant L. Forster, D. E. Oram, Charel Wohl, P. M. Edwards et al.
2 citations
Geophysical Research Letters
Atmospheric chemistry and aerosols
2.60
article

Methanethiol Abundance and Oxidation in a Polluted Marine Atmosphere

Grant L. Forster, D. E. Oram, Charel Wohl, P. M. Edwards, Parvadha Suntharalingam
article en
2 citations

Abstract

Abstract Biological activity in the surface ocean leads to emissions of methanethiol (MeSH) and dimethyl sulfide (DMS). Measurements of MeSH in the marine atmosphere are sparse and the impact of NO x pollution on MeSH oxidation remains unexplored. We present measurements of MeSH and DMS at a coastal site with NO x up to 24.3 ppb in the United Kingdom during May and June. Winds coming from the seaward (northerly) direction showed a median (25th quantiles) MeSH mixing ratio of 15.7 (7.9–26.9) ppt. The measurements reveal significantly lower MeSH during daytime. Atmospheric box model calculations suggest that ∼25% of the MeSH oxidation is initiated by NO 3 at this site and that NO x pollution can reduce the SO 2 yield from MeSH. This work is further evidence for the prevalence of MeSH and illustrates the impact of NO x pollution on MeSH oxidation with associated implications for its role in aerosol‐cloud processes, and climate.

Geophysical Research LettersVol. 52(8)
University of East Anglia (GB), National Centre for Atmospheric Science (GB), University of York (GB)
UK Research and Innovation, National Centre for Atmospheric Science, Natural Environment Research Council
Openalex Percentile: Top 12%
Atmospheric chemistry and aerosols
2.60
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Methanethiol Abundance and Oxidation in a Polluted Marine Atmosphere — Grant L. Forster, D. E. Oram, et al. · Geophysical Research Letters (2025) | TGRS Research Map | TGRS