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The Surface Ocean-Lower Atmosphere Study (SOLAS) is a global research network dedicated to advancing coupled oceanographic and atmospheric science, a field that requires both interdisciplinary and globally distributed expertise. Since 2004, SOLAS has fostered an international interdisciplinary scientific community through coordinated science and capacity sharing activities. This paper outlines how SOLAS 3.0 (2026–2035) will build on this legacy by further prioritizing diversity, equity, and inclusion, and expanding and strengthening research at the ocean-​atmosphere interface. SOLAS 3.0 new initiatives include a mentorship program, skill enhancement workshops, increasing access to resources, and a network of observation and training centers. By learning from past successes and challenges, SOLAS 3.0 aims to inspire scientists from around the world, as well as the next generation, to address complex transdisciplinary research and tackle present and future societal challenges in a truly global way. 

This perspective piece on aerosol deposition to marine ecosystems and the related impacts on biogeochemical cycles forms part of a larger Surface Ocean Lower Atmosphere Study status-of-the-science special edition. A large body of recent reviews has comprehensively covered different aspects of this topic. Here, we aim to take a fresh approach by reviewing recent research to identify potential foundations for future study. We have purposefully chosen to discuss aerosol nutrient and pollutant fluxes both in terms of the journey that different aerosol particles take and that of the surrounding scientific field exploring them. To do so, we explore some of the major tools, knowledge, and partnerships we believe are required to aid advancing this highly interdisciplinary field of research. We recognize that significant gaps persist in our understanding of how far aerosol deposition modulates marine biogeochemical cycles and thus climate. This uncertainty increases as socioeconomic pressures, climate change, and technological advancements continue to change how we live and interact with the marine environment. Despite this, recent advances in modeling techniques, satellite remote sensing, and field observations have provided valuable insights into the spatial and temporal variability of aerosol deposition across the world’s ocean. With the UN Ocean Decade and sustainable development goals in sight, it becomes essential that the community prioritizes the use of a wide variety of tools, knowledge, and partnerships to advance understanding. It is through a collaborative and sustained effort that we hope the community can address the gaps in our understanding of the complex interactions between aerosol particles, marine ecosystems, and biogeochemical cycles. 

Abstract. The oxidation of dimethyl sulfide (DMS;CH3SCH3), emitted from the surface ocean, contributes to theformation of Aitken mode particles and their growth to cloud condensationnuclei (CCN) sizes in remote marine environments. It is not clear whetherother less commonly measured marine-derived, sulfur-containing gases sharesimilar dynamics to DMS and contribute to secondary marine aerosolformation. Here, we present measurements of gas-phase volatile organosulfurmolecules taken with a Vocus proton-transfer-reaction high-resolutiontime-of-flight mass spectrometer during a mesocosm phytoplankton bloomexperiment using coastal seawater. We show that DMS, methanethiol (MeSH;CH3SH), and benzothiazole (C7H5NS) account for on averageover 90 % of total gas-phase sulfur emissions, with non-DMS sulfur sourcesrepresenting 36.8 ± 7.7 % of sulfur emissions during the first 9 d of the experiment in the pre-bloom phase prior to major biologicalgrowth, before declining to 14.5 ± 6.0 % in the latter half of theexperiment when DMS dominates during the bloom and decay phases. The molarratio of DMS to MeSH during the pre-bloom phase (DMS : MeSH = 4.60 ± 0.93) was consistent with the range of previously calculated ambient DMS-to-MeSH sea-to-air flux ratios. As the experiment progressed, the DMS to MeSHemission ratio increased significantly, reaching 31.8 ± 18.7 duringthe bloom and decay. Measurements of dimethylsulfoniopropionate (DMSP),heterotrophic bacteria, and enzyme activity in the seawater suggest theDMS : MeSH ratio is a sensitive indicator of the bacterial sulfur demand andthe composition and magnitude of available sulfur sources in seawater. Theevolving DMS : MeSH ratio and the emission of a new aerosol precursor gas,benzothiazole, have important implications for secondary sulfate formationpathways in coastal marine environments. 

Abstract. Ice-nucleating particles (INPs) represent a rare subset of aerosol particlesthat initiate cloud droplet freezing at temperatures above the homogenousfreezing point of water (−38 ∘C). Considering that the oceancovers 71 % of the Earth's surface and represents a large potential sourceof INPs, it is imperative that the identities, properties and relativeemissions of ocean INPs become better understood. However, the specificunderlying drivers of marine INP emissions remain largely unknown due tolimited observations and the challenges associated with isolating rare INPs. Bygenerating isolated nascent sea spray aerosol (SSA) over a range ofbiological conditions, mesocosm studies have shown that marine microbes cancontribute to INPs. Here, we identify 14 (30 %) cultivable halotolerantice-nucleating microbes and fungi among 47 total isolates recovered fromprecipitation and aerosol samples collected in coastal air in southernCalifornia. Ice-nucleating (IN) isolates collected in coastal air were nucleated ice fromextremely warm to moderate freezing temperatures (−2.3 to −18 ∘C). While some Gammaproteobacteria and fungi are known to nucleate ice attemperatures as high as −2 ∘C, Brevibacterium sp. is the first Actinobacteriafound to be capable of ice nucleation at a relatively high freezingtemperature (−2.3 ∘C). Air mass trajectory analysis demonstratesthat marine aerosol sources were dominant during all sampling periods, andphylogenetic analysis indicates that at least 2 of the 14 IN isolates areclosely related to marine taxa. Moreover, results from cell-washingexperiments demonstrate that most IN isolates maintained freezing activityin the absence of nutrients and cell growth media. This study supportsprevious studies that implicated microbes as a potential source of marineINPs, and it additionally demonstrates links between precipitation, marineaerosol and IN microbes. 

Marine aerosols strongly influence climate through their interactions with solar radiation and clouds. However, significant questions remain regarding the influences of biological activity and seawater chemistry on the flux, chemical composition, and climate-relevant properties of marine aerosols and gases. Wave channels, a traditional tool of physical oceanography, have been adapted for large-scale ocean-atmosphere mesocosm experiments in the laboratory. These experiments enable the study of aerosols under controlled conditions which isolate the marine system from atmospheric anthropogenic and terrestrial influences. Here, we present an overview of the 2019 Sea Spray Chemistry and Particle Evolution (SeaSCAPE) study, which was conducted in an 11 800 L wave channel which was modified to facilitate atmospheric measurements. The SeaSCAPE campaign sought to determine the influence of biological activity in seawater on the production of primary sea spray aerosols, volatile organic compounds (VOCs), and secondary marine aerosols. Notably, the SeaSCAPE experiment also focused on understanding how photooxidative aging processes transform the composition of marine aerosols. In addition to a broad range of aerosol, gas, and seawater measurements, we present key results which highlight the experimental capabilities during the campaign, including the phytoplankton bloom dynamics, VOC production, and the effects of photochemical aging on aerosol production, morphology, and chemical composition. Additionally, we discuss the modifications made to the wave channel to improve aerosol production and reduce background contamination, as well as subsequent characterization experiments. The SeaSCAPE experiment provides unique insight into the connections between marine biology, atmospheric chemistry, and climate-relevant aerosol properties, and demonstrates how an ocean-atmosphere-interaction facility can be used to isolate and study reactions in the marine atmosphere in the laboratory under more controlled conditions.