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Seasonal cycling in carbon, alkalinity, and nutrients in landfast sea ice in Hangar Cove, Adelaide Island, West Antarctic Peninsula, were investigated during winter, spring, and summer 2014–2015. Temporal dynamics were driven by changes in the sea‐ice physicochemical conditions, ice‐algal community composition, and organic matter production. Winter sea ice was enriched with dissolved inorganic carbon (DIC) and inorganic nutrients from organic matter remineralization. Variations in alkalinity (Alk) and DIC indicated that abiotic calcium carbonate (ikaite) precipitation had taken place. Relative to other nutrients, low phosphate (PO4) concentrations potentially resulted from co‐precipitation with ikaite. Seawater flooding and meltwater induced variability in the physical and biogeochemical properties in the upper ice in spring where nutrient resupply supported haptophyte productivity and increased particulate organic carbon (POC) in the interstitial layer. Rapid nitrate (NO3) and DIC (< 165 μmol kg−1) uptake occurred alongside substantial build‐up of algal biomass (746 μg chlorophyll aL−1) and POC (6191 μmol L−1) during summer. Silicic acid drawdown followed NO3depletion by approximately 1 month with a shift to diatom‐dominated communities. Accumulation of PO4in the lower ice layers in summer likely resulted from PO4released during ikaite dissolution in the presence of biofilms. Increased Alk : DIC ratios in the lower ice and under‐ice water suggested that ikaite dissolution buffered against meltwater dilution and enhanced the potential for atmospheric CO2uptake. This study revealed strong seasonality in carbon and nutrient cycling in landfast sea ice and showed the importance of sea ice in biogeochemical cycling in seasonally ice‐covered waters around Antarctica.

The Arctic sea-ice-scape is rapidly transforming. Increasing light penetration will initiate earlier seasonal primary production. This earlier growing season may be accompanied by an increase in ice algae and phytoplankton biomass, augmenting the emission of dimethylsulfide and capture of carbon dioxide. Secondary production may also increase on the shelves, although the loss of sea ice exacerbates the demise of sea-ice fauna, endemic fish and megafauna. Sea-ice loss may also deliver more methane to the atmosphere, but warmer ice may release fewer halogens, resulting in fewer ozone depletion events. The net changes in carbon drawdown are still highly uncertain. Despite large uncertainties in these assessments, we expect disruptive changes that warrant intensified long-term observations and modelling efforts.

Coastal zones of Antarctica harbor rich but highly variable phytoplankton communities. The mechanisms that control the dynamics of these communities are not well defined. Here we elucidate the mechanisms that drive seasonal species succession, based on algal photophysiological characteristics and environmental factors. For this, phytoplankton community structure together with oceanographic parameters was studied over a 5‐year period (2012–2017) at Rothera Station at Ryder Bay (Western Antarctic Peninsula). Algal pigment patterns and photophysiological studies based on fluorescence analyses were combined with data from the Rothera Time‐Series program. Considerable interannual variation was observed, related to variations in wind‐mixing, ice cover and an El Niño event. Clear patterns in the succession of algal classes became manifest when combining the data collected over the five successive years. In spring, autotrophic flagellates with a high light affinity were the first to profit from increasing light and sea ice melt. These algae most likely originated from sea‐ice communities, stressing the role of sea ice as a seeding vector for the spring bloom. Diatoms became dominant towards summer in more stratified and warmer surface waters. These communities displayed significantly lower photoflexibility than spring communities. There are strong indications for mixotrophy in cryptophytes, which would explain much of their apparently random occurrence. Climate models predict continuing retreat of Antarctic sea‐ice during the course of this century. For the near‐future we predict that the marginal sea‐ice zone will still harbor significant communities of haptophytes and chlorophytes, whereas increasing temperatures will mainly be beneficial for diatoms.

Predictions of the ocean‐atmosphere flux of dimethyl sulfide will be improved by understanding what controls seasonal and regional variations in dimethylsulfoniopropionate (DMSP) production. To investigate the influence of high levels of irradiance including ultraviolet radiation (UVR), on DMSP synthesis rates (μDMSP) and inorganic carbon fixation (μPOC) by natural phytoplankton communities, nine experiments were carried out at different locations in the low nutrient, high light environment of the northeastern Tropical Atlantic. Rates of μDMSP and μPOC were determined by measuring the incorporation of inorganic 13C into DMSP and particulate organic carbon. Based on measurements over discrete time intervals during the day, a unique μDMSP vs. irradiance (P vs. E) relationship was established. Comparison is made with the P vs. E relationship for μPOC, indicating that light saturation of μDMSP occurs at similar irradiance to μPOC and is closely coupled to carbon fixation on a diel basis. Photoinhibition during the middle of the day was exacerbated by exposure to UVR, causing an additional 55–60% inhibition of both μDMSP and μPOC at the highest light levels. In addition, decreased production of DMSP in response to UVR‐induced photoxidative stress, contrasted with the increased net synthesis of photoprotective xanthophyll pigments. Together these results indicate that DMSP production by phytoplankton in the tropical ocean is not regulated in the short term by the necessity to control increasing photooxidative stress as irradiance increases during the day. The study provides new insight into the regulation of resource allocation into this biogeochemically important, multi‐functional compatible solute.

Environmental context Understanding the exchange of energy, gases and particles at the ocean–atmosphere interface is critical for the development of robust predictions of, and response to, future climate change. The international Surface Ocean–Lower Atmosphere Study (SOLAS) coordinates multi-disciplinary ocean–atmosphere research projects that quantify and characterise this exchange. This article details five new SOLAS research strategies – upwellings and associated oxygen minimum zones, sea ice, marine aerosols, atmospheric nutrient supply and ship emissions – that aim to improve knowledge in these critical areas. Abstract This review focuses on critical issues in ocean–atmosphere exchange that will be addressed by new research strategies developed by the international Surface Ocean–Lower Atmosphere Study (SOLAS) research community. Eastern boundary upwelling systems are important sites for CO2 and trace gas emission to the atmosphere, and the proposed research will examine how heterotrophic processes in the underlying oxygen-deficient waters interact with the climate system. The second regional research focus will examine the role of sea-ice biogeochemistry and its interaction with atmospheric chemistry. Marine aerosols are the focus of a research theme directed at understanding the processes that determine their abundance, chemistry and radiative properties. A further area of aerosol-related research examines atmospheric nutrient deposition in the surface ocean, and how differences in origin, atmospheric processing and composition influence surface ocean biogeochemistry. Ship emissions are an increasing source of aerosols, nutrients and toxins to the atmosphere and ocean surface, and an emerging area of research will examine their effect on ocean biogeochemistry and atmospheric chemistry. The primary role of SOLAS is to coordinate coupled multi-disciplinary research within research strategies that address these issues, to achieve robust representation of critical ocean–atmosphere exchange processes in Earth System models.