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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. 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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3. 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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4. Cloud Microphysical Effects of Aerosol Particle Sources and Marine Boundary Layer Processes

   Sanchez, Kevin J (January 2017, UC San Diego Electronic Theses and Dissertations)

   Marine boundary layer (MBL) clouds are an important, though uncertain, part of Earth’s radiative budget. Previous studies have shown sources of aerosol particles in the remote MBL consist of primary sea spray, the oxidation of organic and inorganic vapors derived from the ocean, entrainment from the free troposphere, and anthropogenic pollution. The potential for these particles to become cloud condensation nuclei (CCN) varies largely dependent on their hygroscopic properties. Furthermore, when clouds form, physical processes can alter the optical properties of the cloud. This dissertation aims to identify variations in aerosol sources that affect MBL CCN concentrations and physical processes throughout the cloud lifetime that influence cloud optical properties. Ambient measurements of marine particles and clouds were made throughout two campaigns in the north Pacific and four campaigns in the north Atlantic. Both clean marine and polluted clouds were sampled. In addition, dry MBL particles were measured to identify their chemical composition and size distribution, which is necessary to identify their potential to be CCN active. The organic hygroscopicity influenced CCN concentrations and cloud optical properties significantly for particles that were mostly organic, such as ship stack and generated smoke particles. For a typical range of organic hygroscopicity the amount of reflected solar radiation varied by 2-7% for polluted conditions and less than 1% for clean conditions. Simulated droplet spectral width was shown to be more representative of observations when using a weighted distribution of cloud base heights and updraft velocities, and increased the cloud reflectivity up to 2%. Cloud top entrainment and decoupling of the MBL were found to account for a decrease in cloud radiative forcing. Cloud top entrainment was corrected for homogeneous entrainment and accounted for a decrease in radiative forcing of up to 50 Wm-2. Clustering of individual marine aerosol particles resulted in the identification of particle types derived from dimethyl-sulfide (DMS) oxidation. Two particle types were identified to come from DMS oxidation products and accounted for approximately 25% and 65% of CCN at 0.1% supersaturation during the winter and summer, respectively. One of the particle types was found to be entrained from the free troposphere. 

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5. Oceanic emissions of dimethyl sulfide and methanethiol and their contribution to sulfur dioxide production in the marine atmosphere

   https://doi.org/10.5194/acp-22-6309-2022  

   Novak, Gordon A.; Kilgour, Delaney B.; Jernigan, Christopher M.; Vermeuel, Michael P.; Bertram, Timothy H. (January 2022, Atmospheric Chemistry and Physics)

   Abstract. Oceanic emissions of dimethyl sulfide (CH3SCH3,DMS) have long been recognized to impact aerosol particle composition andsize, the concentration of cloud condensation nuclei (CCN), and Earth'sradiation balance. The impact of oceanic emissions of methanethiol(CH3SH, MeSH), which is produced by the same oceanic precursor as DMS,on the volatile sulfur budget of the marine atmosphere is largelyunconstrained. Here we present direct flux measurements of MeSH oceanicemissions using the eddy covariance (EC) method with a high-resolutionproton-transfer-reaction time-of-flight mass spectrometer (PTR-ToFMS)detector and compare them to simultaneous flux measurements of DMS emissionsfrom a coastal ocean site. Campaign mean mixing ratios of DMS and MeSH were72 ppt (28–90 ppt interquartile range) and 19.1 ppt (7.6–24.5 pptinterquartile range), respectively. Campaign mean emission fluxes of DMS (FDMS) and MeSH (FMeSH) were 1.13 ppt m s−1 (0.53–1.61 ppt m s−1 interquartile range) and 0.21 ppt m s−1 (0.10–0.31 ppt m s−1 interquartile range), respectively. Linear least squares regression of observed MeSH and DMS flux indicates the emissions are highly correlatedwith each other (R2=0.65) over the course of the campaign,consistent with a shared oceanic source. The campaign mean DMS to MeSH fluxratio (FDMS:FMeSH) was 5.5 ± 3.0, calculated from the ratio of 304 individual coincident measurements of FDMS and FMeSH. Measured FDMS:FMeSH was weakly correlated (R2=0.15) withocean chlorophyll concentrations, with FDMS:FMeSH reaching a maximumof 10.8 ± 4.4 during a phytoplankton bloom period. No other volatilesulfur compounds were observed by PTR-ToFMS to have a resolvable emissionflux above their flux limit of detection or to have a gas-phase mixing ratio consistently above their limit of detection during the study period,suggesting DMS and MeSH are the dominant volatile organic sulfur compoundsemitted from the ocean at this site. The impact of this MeSH emission source on atmospheric budgets of sulfurdioxide (SO2) was evaluated by implementing observed emissions in a coupled ocean–atmosphere chemical box model using a newly compiled MeSHoxidation mechanism. Model results suggest that MeSH emissions lead toafternoon instantaneous SO2 production of 2.5 ppt h−1, which results in a 43 % increase in total SO2 production compared to a casewhere only DMS emissions are considered and accounts for 30% of theinstantaneous SO2 production in the marine boundary layer at the meanmeasured FDMS and FMeSH. This contribution of MeSH to SO2production is driven by a higher effective yield of SO2 from MeSHoxidation and the shorter oxidation lifetime of MeSH compared to DMS. Thislarge additional source of marine SO2 has not been previouslyconsidered in global models of marine sulfur cycling. The field measurementsand modeling results presented here demonstrate that MeSH is an importantcontributor to volatile sulfur budgets in the marine atmosphere and must be measured along with DMS in order to constrain marine sulfur budgets. Thislarge additional source of marine–reduced sulfur from MeSH will contribute to particle formation and growth and CCN abundance in the marine atmosphere, with subsequent impacts on climate. 

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