Your search

Future mass loss from the East Antarctic Ice Sheet represents a major uncertainty in projections of future sea level rise. Recent studies have highlighted the potential vulnerability of the East Antarctic Ice Sheet to atmospheric and oceanic changes, but long-term observations inside the ice shelf cavities are rare. Here, we present new insights from observations from three oceanic moorings below Fimbulisen Ice Shelf from 2009 to 2023. We examine the characteristics of intrusions of modified Warm Deep Water (mWDW) across a sill connecting the cavity to the open ocean and investigate seasonal variability of the circulation and water masses inside the cavity using an optimum multiparameter analysis. In autumn, the water below the 345 m deep central part of the ice shelf is composed of up to 30 % solar-heated, buoyant Antarctic Surface Water (ASW), separating colder Ice Shelf Water from the ice base and affecting the cavity circulation on seasonal timescales. At depth, the occurrence of mWDW is associated with the advection of cyclonic eddies across the sill into the cavity. These eddies reach up to the ice base. The warm intrusions are observed most often from January to March and from September to November, and traces of mWDW-derived meltwater close to the ice base imply an overturning of these warm intrusions inside the cavity. We suggest that this timing is set by both the offshore thermocline depth and the interactions of the Antarctic Slope Current with the ice shelf topography over the continental slope. Our findings provide a better understanding of the interplay between shallow inflows of ASW contributions and deep inflows of mWDW for basal melting at Fimbulisen Ice Shelf, with implications for the potential vulnerability of the ice shelf to climate change.

Sea surface fugacity of carbon dioxide (fCO₂ssw) was measured across the Weddell gyre and the eastern sector in the Atlantic Southern Ocean in autumn. During the occupation between February and April 2019, the region of the study transect was a potential ocean CO₂ sink. A net CO₂ flux (FCO₂) of −6.2 (± 8; sink) mmol m^–2 d^–1 was estimated for the entire study region, with the largest average CO₂ sink of −10.0 (± 8) mmol m^–2 d^–1 in the partly ice-covered Astrid Ridge (AR) region near the coast at 68°S and −6.1 (± 8) mmol m^–2d^–1 was observed in the Maud Rise (MR) region. A CO₂ sink was also observed south of 66°S in the Weddell Sea (WS). To assess the main drivers describing the variability of fCO₂ssw, a correlation model using fCO₂ and oxygen saturation was considered. Spatial distributions of the fCO₂ saturation/O₂ saturation correlations, described relative to the surface water properties of the controlling variables (chlorophyll a, apparent oxygen utilization (AOU), sea surface temperature, and sea surface salinity) further constrained the interplay of the processes driving the fCO₂ssw distributions. Photosynthetic CO₂ drawdown significantly offsets the influence of the upwelling of CO₂-rich waters in the central Weddell gyre and enhanced the CO₂ sink in the region. FCO₂ of −6.9 mmol m^–2 d^–1 estimated for the Weddell gyre in this study was different from FCO₂ of −2.5 mmol m^–2 d^–1 in autumn estimated in a previous study. Due to low CO₂ data coverage during autumn, limited sea-air CO₂ flux estimates from direct sea-surface CO₂ observations particularly for the Weddell gyre region are available with which to compare the values estimated in this study. This highlights the importance of increasing seasonal CO₂ observations especially during autumn/winter to improving the seasonal coverage of flux estimates in the seasonal sea ice-covered regions of the Southern Ocean.

Iron(III) photoreduction and the responses of phytoplankton under ultraviolet (UV) and photosynthetically available radiation (PAR) were investigated with the presence of hydroxycarboxylic acid (glucaric acid (GA), a model compound for organic acids excreted by phytoplankton). The incubation experiments were carried out on board using seawater samples collected in the location of the winter ice edge (WIE) and the spring ice edge (SIE) of the Southern Ocean. In this paper, we focus on the results of experiment in WIE. Throughout the experiments, dissolved Fe(II), major nutrients and in vivo fluorescence were monitored regularly. In addition, Chl-a, POC/PON, cell densities of phytoplankton and bacteria, bacterial production, organic peroxide, hydrogen peroxide and total CO2 were measured. The results from the WIE show that iron enrichment had a substantial effect on phytoplankton growth rate. Fe(III) addition in the presence of GA (FeGA) gave higher Fe(II) concentration and higher growth rate of phytoplankton than those in controls. Our results suggest that hydroxycarboxylic acid had a significant chemical and biological impact. The presence of GA influenced iron photochemistry and iron availability to phytoplankton. Phytoplankton growth responses to iron enrichments in incubations under UV and PAR were completely dissimilar. It seems that FeGA addition prominently changes the harmful effect of UV on the phytoplankton population. This study provides preliminary information on how the photoreduction of iron(III) and the phytoplankton growth are affected by iron enrichment in the presence of hydroxycarboxylic acid.

Physiological characteristics of inorganic C uptake were examined in Southern Ocean ice algae and phytoplankton assemblages. Ice algal and phytoplankton assemblages were largely dominated by diatoms and Phaeocystis antarctica, and showed a high capacity for HCO3- utilization, with direct HCO3- transport accounting for ~60% of total inorganic C uptake. Extracellular carbonic anhydrase (eCA) was detectable in all samples, but with significantly lower activity in sea ice algae. Neither HCO3- transport nor eCA activity was related to the in situ partial pressure of CO2 (pCO2) or taxonomic composition of samples. The half-saturation constant (KS) for inorganic C ranged from ~100 to 5000 µM, and showed significantly more variability among sea ice algae than phytoplankton assemblages. For the phytoplankton assemblages, there were significant positive correlations between in situ pCO2 and KS (higher C substrate affinity in low pCO2 waters), and also between KS and maximum C uptake rates (Vmax). In contrast, KS and Vmax in sea-ice algal assemblages were not correlated to each other, or to any other measured variables. The C isotope composition of particulate organic carbon(δ13C-POC) in the phytoplankton assemblages showed modest variability (range -30 to -24.6‰) and was significantly correlated to the ratio of inferred growth rates (derived from Vmax) and in situ CO2 concentrations, but not to any measured C uptake parameters. δ13C-POC in sea ice algal samples (range -25.7 to -12.9‰) was significantly heavier than in the phytoplankton assemblages, and not correlated to any other variables. Our results provide evidence for the widespread occurrence of carbon-concentrating mechanisms in Southern Ocean sea ice algae and phytoplankton assemblages. KEYWORDS: Phytoplankton · Sea ice algae · Inorganic carbon uptake · HCO3- · Carbonic anhydrase

The existence of ice-edge phytoplankton blooms in the Southern Ocean is well described, yet direct observations of the mechanisms of phytoplankton bloom development following seasonal sea-ice melt remain scarce. This study constrains such responses using biological and biogeochemical datasets collected along a coastal-to-offshore transect that bisects the receding sea-ice zone in the Kong Håkon VII Hav (off the coast of Dronning Maud Land). We documented that the biogeochemical growing conditions for phytoplankton vary on a latitudinal gradient of sea-ice concentration, where increased sea-ice melting creates optimal conditions for growth with increased light availability and potentially increased iron supply. The zones of the study area with the least ice cover were associated with diatom dominance, the greatest chlorophyll a concentrations, net community production, and dissolved inorganic carbon drawdown, as well as lower sea surface fugacity of CO2. Together, these associations imply higher potential for an oceanic CO2 sink due, at least in part, to more advanced bloom phase and/or larger bloom magnitude stemming from a relatively longer period of light exposure, as compared to the more ice-covered zones in the study area. From stable oxygen isotope fractions, sea-ice meltwater fractions were highest in the open ocean zone and meteoric meltwater fractions were highest in the coastal and polynya zones, suggesting that potential iron sources may also change on a latitudinal gradient across the study area. Variable phytoplankton community compositions were related to changing sea-ice concentrations, with a typical species succession from sympagic flagellate species (Pyramimonas sp. and Phaeocystis antarctica) to pelagic diatoms (e.g., Dactyliosolen tenuijunctus) observed across the study area. These results fill a spatiotemporal gap in the Southern Ocean, as sea-ice melting plays a larger role in governing phytoplankton bloom dynamics in the future Southern Ocean due to changing sea-ice conditions caused by anthropogenic global warming.

Knowing the magnitude and timing of pelagic primary production is important for ecosystem and carbon sequestration studies, in addition to providing basic understanding of phytoplankton functioning. In this study we use data from an ecosystem cruise to Kong Håkon VII Hav, in the Atlantic sector of the Southern Ocean, in March 2019 and more than two decades of satellite-derived ocean color to study phytoplankton bloom phenology. During the cruise we observed phytoplankton blooms in different bloom phases. By correlating bloom phenology indices (i.e., bloom initiation and end) based on satellite remote sensing to the timing of changes in environmental conditions (i.e., sea ice, light, and mixed layer depth) we studied the environmental factors that seemingly drive phytoplankton blooms in the area. Our results show that blooms mainly take place in January and February, consistent with previous studies that include the area. Sea ice retreat controls the bloom initiation in particular along the coast and the western part of the study area, whereas bloom end is not primarily connected to sea ice advance. Light availability in general is not appearing to control the bloom termination, neither is nutrient availability based on the autumn cruise where we observed non-depleted macronutrient reservoirs in the surface. Instead, we surmise that zooplankton grazing plays a potentially large role to end the bloom, and thus controls its duration. The spatial correlation of the highest bloom magnitude with marked topographic features indicate that the interaction of ocean currents with sea floor topography enhances primary productivity in this area, probably by natural fertilization. Based on the bloom timing and magnitude patterns, we identified five different bloom regimes in the area. A more detailed understanding of the region will help to highlight areas with the highest relevance for the carbon cycle, the marine ecosystem and spatial management. With this gained understanding of bloom phenology, it will also be possible to study potential shifts in bloom timing and associated trophic mismatch caused by environmental changes.

Antarctic sea ice plays an important role in Southern Ocean biogeochemistry and mediating Earth's climate system. Yet our understanding of biogeochemical cycling in sea ice is limited by the availability of relevant data over sufficient temporal and spatial scales. Here we present a new publicly available compilation of macronutrient concentration data from Antarctic land-fast sea ice, covering the full seasonal cycle using datasets from around Antarctica, as well as a smaller dataset of macronutrient concentrations in adjacent seawater. We show a strong seasonal cycle whereby nutrient concentrations are high during autumn and winter, due to supply from underlying surface waters, and then are utilised in spring and summer by mixed ice algal communities consisting of diatoms and non-siliceous species. Our data indicate some degree of nutrient limitation of ice algal primary production, with silicon limitation likely being most prevalent, although uncertainties remain around the affinities of sea-ice algae for each nutrient. Remineralisation of organic matter and nutrient recycling drive substantial accumulations of inorganic nitrogen, phosphate and to a lesser extent silicic acid in some ice cores to concentrations far in excess of those in surface waters. Nutrient supply to fast ice is enhanced by brine convection, platelet ice accumulation and incorporation into the ice matrix, and under-ice tidal currents, whilst nutrient adsorption to sea-ice surfaces, formation of biofilms, and abiotic mineral precipitation and dissolution can also influence fast-ice nutrient cycling. Concentrations of nitrate, ammonium and silicic acid were generally higher in fast ice than reported for Antarctic pack ice, and this may support the typically observed higher algal biomass in fast-ice environments.

Despite the exclusion of the Southern Ocean from assessments of progress towards achieving the Convention on Biological Diversity (CBD) Strategic Plan, the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR) has taken on the mantle of progressing efforts to achieve it. Within the CBD, Aichi Target 11 represents an agreed commitment to protect 10% of the global coastal and marine environment. Adopting an ethos of presenting the best available scientific evidence to support policy makers, CCAMLR has progressed this by designating two Marine Protected Areas in the Southern Ocean, with three others under consideration. The region of Antarctica known as Dronning Maud Land (DML; 20°W to 40°E) and the Atlantic sector of the Southern Ocean that abuts it conveniently spans one region under consideration for spatial protection. To facilitate both an open and transparent process to provide the vest available scientific evidence for policy makers to formulate management options, we review the body of physical, geochemical and biological knowledge of the marine environment of this region. The level of scientific knowledge throughout the seascape abutting DML is polarized, with a clear lack of data in its eastern part which is presumably related to differing levels of research effort dedicated by national Antarctic programmes in the region. The lack of basic data on fundamental aspects of the physical, geological and biological nature of eastern DML make predictions of future trends difficult to impossible, with implications for the provision of management advice including spatial management. Finally, by highlighting key knowledge gaps across the scientific disciplines our review also serves to provide guidance to future research across this important region.

A rigorous synthesis of the sea-ice ecosystem and linked ecosystem services highlights that the sea-ice ecosystem supports all 4 ecosystem service categories, that sea-ice ecosystems meet the criteria for ecologically or biologically significant marine areas, that global emissions driving climate change are directly linked to the demise of sea-ice ecosystems and its ecosystem services, and that the sea-ice ecosystem deserves specific attention in the evaluation of marine protected area planning. The synthesis outlines (1) supporting services, provided in form of habitat, including feeding grounds and nurseries for microbes, meiofauna, fish, birds and mammals (particularly the key species Arctic cod, Boreogadus saida, and Antarctic krill, Euphausia superba, which are tightly linked to the sea-ice ecosystem and transfer carbon from sea-ice primary producers to higher trophic level fish, mammal species and humans); (2) provisioning services through harvesting and medicinal and genetic resources; (3) cultural services through Indigenous and local knowledge systems, cultural identity and spirituality, and via cultural activities, tourism and research; (4) (climate) regulating services through light regulation, the production of biogenic aerosols, halogen oxidation and the release or uptake of greenhouse gases, for example, carbon dioxide. The ongoing changes in the polar regions have strong impacts on sea-ice ecosystems and associated ecosystem services. While the response of sea-ice–associated primary production to environmental change is regionally variable, the effect on ice-associated mammals and birds is predominantly negative, subsequently impacting human harvesting and cultural services in both polar regions. Conservation can help protect some species and functions. However, the key mitigation measure that can slow the transition to a strictly seasonal ice cover in the Arctic Ocean, reduce the overall loss of sea-ice habitats from the ocean, and thus preserve the unique ecosystem services provided by sea ice and their contributions to human well-being is a reduction in carbon emissions.

The Southern Ocean is a major sink of anthropogenic CO2 and an important foraging area for top trophic level consumers. However, iron limitation sets an upper limit to primary productivity. Here we report on a considerably dense late summer phytoplankton bloom spanning 9000 km2 in the open ocean of the eastern Weddell Gyre. Over its 2.5 months duration, the bloom accumulated up to 20 g C m−2 of organic matter, which is unusually high for Southern Ocean open waters. We show that, over 1997–2019, this open ocean bloom was likely driven by anomalies in easterly winds that push sea ice southwards and favor the upwelling of Warm Deep Water enriched in hydrothermal iron and, possibly, other iron sources. This recurring open ocean bloom likely facilitates enhanced carbon export and sustains high standing stocks of Antarctic krill, supporting feeding hot spots for marine birds and baleen whales.