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1. Contribution of expanded marine sulfur chemistry to the seasonal variability of dimethyl sulfide oxidation products and size-resolved sulfate aerosol

   https://doi.org/10.5194/acp-24-3379-2024  

   Tashmim, Linia; Porter, William C; Chen, Qianjie; Alexander, Becky; Fite, Charles H; Holmes, Christopher D; Pierce, Jeffrey R; Croft, Betty; Ishino, Sakiko (January 2024, Atmospheric Chemistry and Physics)

   Abstract. Marine emissions of dimethyl sulfide (DMS) and the subsequent formation of its oxidation products methanesulfonic acid (MSA) and sulfuric acid (H2SO4) are well-known natural precursors of atmospheric aerosols, contributing to particle mass and cloud formation over ocean and coastal regions. Despite a long-recognized and well-studied role in the marine troposphere, DMS oxidation chemistry remains a work in progress within many current air quality and climate models, with recent advances exploring heterogeneous chemistry and uncovering previously unknown intermediate species. With the identification of additional DMS oxidation pathways and intermediate species that influence the eventual fate of DMS, it is important to understand the impact of these pathways on the overall sulfate aerosol budget and aerosol size distribution. In this work, we update and evaluate the DMS oxidation mechanism of the chemical transport model GEOS-Chem by implementing expanded DMS oxidation pathways in the model. These updates include gas- and aqueous-phase reactions, the formation of the intermediates dimethyl sulfoxide (DMSO) and methanesulfinic acid (MSIA), and cloud loss and aerosol uptake of the recently quantified intermediate hydroperoxymethyl thioformate (HPMTF). We find that this updated mechanism collectively decreases the global mean surface-layer gas-phase sulfur dioxide (SO2) mixing ratio by 40 % and enhances the sulfate aerosol (SO42-) mixing ratio by 17 %. We further perform sensitivity analyses exploring the contribution of cloud loss and aerosol uptake of HPMTF to the overall sulfur budget. Comparing modeled concentrations to available observations, we find improved biases relative to previous studies. To quantify the impacts of these chemistry updates on global particle size distributions and the mass concentration, we use the TwO-Moment Aerosol Sectional (TOMAS) aerosol microphysics module coupled to GEOS-Chem and find that changes in particle formation and growth affect the size distribution of aerosol. With this new DMS-oxidation scheme, the global annual mean surface-layer number concentration of particles with diameters smaller than 80 nm decreases by 16.8 %, with cloud loss processes related to HPMTF being mostly responsible for this reduction. However, the global annual mean number of particles larger than 80 nm (corresponding to particles capable of acting as cloud condensation nuclei, CCN) increases by 3.8 %, suggesting that the new scheme promotes seasonal particle growth to these sizes. 

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2. Global airborne sampling reveals a previously unobserved dimethyl sulfide oxidation mechanism in the marine atmosphere

   https://doi.org/10.1073/pnas.1919344117  

   Veres, Patrick R.; Neuman, J. Andrew; Bertram, Timothy H.; Assaf, Emmanuel; Wolfe, Glenn M.; Williamson, Christina J.; Weinzierl, Bernadett; Tilmes, Simone; Thompson, Chelsea R.; Thames, Alexander B.; et al (March 2020, Proceedings of the National Academy of Sciences)

   Dimethyl sulfide (DMS), emitted from the oceans, is the most abundant biological source of sulfur to the marine atmosphere. Atmospheric DMS is oxidized to condensable products that form secondary aerosols that affect Earth’s radiative balance by scattering solar radiation and serving as cloud condensation nuclei. We report the atmospheric discovery of a previously unquantified DMS oxidation product, hydroperoxymethyl thioformate (HPMTF, HOOCH 2 SCHO), identified through global-scale airborne observations that demonstrate it to be a major reservoir of marine sulfur. Observationally constrained model results show that more than 30% of oceanic DMS emitted to the atmosphere forms HPMTF. Coincident particle measurements suggest a strong link between HPMTF concentration and new particle formation and growth. Analyses of these observations show that HPMTF chemistry must be included in atmospheric models to improve representation of key linkages between the biogeochemistry of the ocean, marine aerosol formation and growth, and their combined effects on climate. 

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3. Global Impacts of Marine Methanethiol Emissions and Chemistry in the Atmosphere

   https://doi.org/10.1021/acs.est.5c02019  

   Tashmim, Linia; Porter, William C; Bertram, Timothy H; Kilgour, Delaney B; Rollins, Andrew (September 2025, Environmental Science & Technology)

   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 eNective yield of SO2 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 SO2 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 SO2 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 eNorts aimed at improving the modeled representation of sulfur spatiotemporal patterns relevant to air quality predictions and climate impact assessments. 

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4. Cloud Processes and the Transport of Biological Emissions Regulate Southern Ocean Particle and Cloud Condensation Nuclei Concentrations

   Sanchez, K. J.; Roberts, G. C.; Saliba, G.; Russell, L. M.; Twohy, C.; Reeves, M.; Humphries, R. S.; Keywood, M. D.; Ward, J. P.; McRobert, I. M. (January 2021, Atmospheric chemistry and physics)

   null (Ed.)

   Long-range transport of biogenic emissions from the coast of Antarctica, precipitation scavenging, and cloud processing are the main processes that influence the observed variability in Southern Ocean (SO) marine boundary layer (MBL) condensation nuclei (CN) and cloud condensation nuclei (CCN) concentrations during the austral summer. Airborne particle measurements on the HIAPER GV from north-south transects between Hobart, Tasmania and 62°S during the Southern Ocean Clouds, Radiation Aerosol Transport Experimental Study (SOCRATES) were separated into four regimes comprising combinations of high and low concentrations of CCN and CN. In 5-day HYSPLIT back trajectories, air parcels with elevated CCN concentrations were almost always shown to have crossed the Antarctic coast, a location with elevated phytoplankton emissions relative to the rest of the SO in the region south of Australia. The presence of high CCN concentrations was also consistent with high cloud fractions over their trajectory, suggesting there was substantial growth of biogenically formed particles through cloud processing. Cases with low cloud fraction, due to the presence of cumulus clouds, had high CN concentrations, consistent with previously reported new particle formation in cumulus outflow regions. Measurements associated with elevated precipitation during the previous 1.5-days of their trajectory had low CCN concentrations indicating CCN were effectively scavenged by precipitation. A coarse-mode fitting algorithm was used to determine the primary marine aerosol (PMA) contribution which accounted for < 20% of CCN (at 0.3% supersaturation) and cloud droplet number concentrations. Vertical profiles of CN and large particle concentrations (Dp > 0.07µm) indicated that particle formation occurs more frequently above the MBL; however, the growth of recently formed particles typically occurs in the MBL, consistent with cloud processing and the condensation of volatile compound oxidation products. 

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5. Measurement report: Cloud processes and the transport of biological emissions affect southern ocean particle and cloud condensation nuclei concentrations

   https://doi.org/10.5194/acp-21-3427-2021  

   Sanchez, Kevin J.; Roberts, Gregory C.; Saliba, Georges; Russell, Lynn M.; Twohy, Cynthia; Reeves, Michael J.; Humphries, Ruhi S.; Keywood, Melita D.; Ward, Jason P.; McRobert, Ian M. (January 2021, Atmospheric Chemistry and Physics)

   null (Ed.)

   Abstract. Long-range transport of biogenic emissions from the coastof Antarctica, precipitation scavenging, and cloud processing are the mainprocesses that influence the observed variability in Southern Ocean (SO)marine boundary layer (MBL) condensation nuclei (CN) and cloud condensationnuclei (CCN) concentrations during the austral summer. Airborne particlemeasurements on the HIAPER GV from north–south transects between Hobart,Tasmania, and 62∘ S during the Southern Ocean Clouds, RadiationAerosol Transport Experimental Study (SOCRATES) were separated into fourregimes comprising combinations of high and low concentrations of CCN andCN. In 5 d HYSPLIT back trajectories, air parcels with elevated CCNconcentrations were almost always shown to have crossed the Antarctic coast,a location with elevated phytoplankton emissions relative to the rest of theSO in the region south of Australia. The presence of high CCN concentrationswas also consistent with high cloud fractions over their trajectory,suggesting there was substantial growth of biogenically formed particlesthrough cloud processing. Cases with low cloud fraction, due to the presenceof cumulus clouds, had high CN concentrations, consistent with previouslyreported new particle formation in cumulus outflow regions. Measurementsassociated with elevated precipitation during the previous 1.5 d of theirtrajectory had low CCN concentrations indicating CCN were effectivelyscavenged by precipitation. A coarse-mode fitting algorithm was used todetermine the primary marine aerosol (PMA) contribution, which accounted for<20 % of CCN (at 0.3 % supersaturation) and cloud dropletnumber concentrations. Vertical profiles of CN and large particleconcentrations (Dp>0.07 µm) indicated that particleformation occurs more frequently above the MBL; however, the growth ofrecently formed particles typically occurs in the MBL, consistent with cloudprocessing and the condensation of volatile compound oxidation products. CCN measurements on the R/V Investigator as part of the second Clouds, Aerosols,Precipitation, Radiation and atmospheric Composition Over the southeRn Ocean(CAPRICORN-2) campaign were also conducted during the same period as theSOCRATES study. The R/V Investigator observed elevated CCN concentrations near Australia,likely due to continental and coastal biogenic emissions. The Antarcticcoastal source of CCN from the south, CCN sources from the midlatitudes, andenhanced precipitation sink in the cyclonic circulation between the Ferreland polar cells (around 60∘ S) create opposing latitudinalgradients in the CCN concentration with an observed minimum in the SObetween 55 and 60∘ S. The SOCRATES airbornemeasurements are not influenced by Australian continental emissions butstill show evidence of elevated CCN concentrations to the south of60∘ S, consistent with biogenic coastal emissions. In addition, alatitudinal gradient in the particle composition, south of the Australianand Tasmanian coasts, is apparent in aerosol hygroscopicity derived from CCNspectra and aerosol particle size distribution. The particles are morehygroscopic to the north, consistent with a greater fraction of sea saltfrom PMA, and less hygroscopic to the south as there is more sulfate andorganic particles originating from biogenic sources in coastal Antarctica. 

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