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The flightless midge Eretmoptera murphyi is thought to be continuing its invasion of Signy Island via the treads of personnel boots. Current boot-wash biosecurity protocols in the Antarctic region rely on microbial biocides, primarily Virkon® S. As pesticides have limited approval for use in the Antarctic Treaty area, we investigated the efficacy of Virkon® S in controlling the spread of E. murphyi using boot-wash simulations and maximum threshold exposures. We found that E. murphyi tolerates over 8 h of submergence in 1% Virkon® S. Higher concentrations increased effectiveness, but larvae still exhibited > 50% survival after 5 h in 10% Virkon® S. Salt and hot water treatments (without Virkon® S) were explored as possible alternatives. Salt water proved ineffective, with mortality only in first-instar larvae across multi-day exposures. Larvae experienced 100% mortality when exposed for 10 s to 50°C water, but they showed complete survival at 45°C. Given that current boot-wash protocols alone are an ineffective control of this invasive insect, we advocate hot water (> 50°C) to remove soil, followed by Virkon® S as a microbial biocide on ‘clean’ boots. Implications for the spread of invasive invertebrates as a result of increased human activity in the Antarctic region are discussed.

Antarctic sea ice has paradoxically become more extensive over the past four decades despite a warming climate. The regional expression of this trend has been linked to changes in vertical redistribution of ocean heat and large-scale wind-field shifts. However, the short length of modern observations has hindered attempts to attribute this trend to anthropogenic forcing or natural variability. Here, we present two new decadal-resolution records of sea ice and sea surface temperatures that document pervasive regional climate heterogeneity in Indian Antarctic sea-ice cover over the last 2,000 years. Data assimilation of our marine records in a climate model suggests that the reconstructed dichotomous regional conditions were driven by the multi-decadal variability of the El Niño Southern Oscillation and Southern Annular Mode (SAM). For example, during an El Niño/SAM– combination, the northward sea-ice transport was reduced while heat advection from the subtropics to the Southern Ocean increased, which resulted in reduced sea-ice extent in the Indian sector as sea ice was compacted along the Antarctic coast. Our results therefore indicate that natural variability is large in the Southern Ocean and suggest that it has played a crucial role in the recent sea-ice trends and their decadal variability in this region.

For procellariiform seabirds, wind and morphology are crucial determinants of flight costs and flight speeds. During chick-rearing, parental seabirds commute frequently to provision their chicks, and their body mass typically changes between outbound and return legs. In Antarctica, the characteristic diurnal katabatic winds, which blow stronger in the mornings, form a natural experimental setup to investigate flight behaviors of commuting seabirds in response to wind conditions. We GPS-tracked three closely related species of sympatrically breeding Antarctic fulmarine petrels, which differ in wing loading and aspect ratio, and investigated their flight behavior in response to wind and changes in body mass. Such information is critical for understanding how species may respond to climate change. All three species reached higher ground speeds (i.e., the speed over ground) under stronger tailwinds, especially on return legs from foraging. Ground speeds decreased under stronger headwinds. Antarctic petrels (Thalassoica antarctica; intermediate body mass, highest wing loading, and aspect ratio) responded stronger to changes in wind speed and direction than cape petrels (Daption capense; lowest body mass, wing loading, and aspect ratio) or southern fulmars (Fulmarus glacialoides; highest body mass, intermediate wing loading, and aspect ratio). Birds did not adjust their flight direction in relation to wind direction nor the maximum distance from their nests when encountering headwinds on outbound commutes. However, birds appeared to adjust the timing of commutes to benefit from strong katabatic winds as tailwinds on outbound legs and avoid strong katabatic winds as headwinds on return legs. Despite these adaptations to the predictable diurnal wind conditions, birds frequently encountered unfavorably strong headwinds, possibly as a result of weather systems disrupting the katabatics. How the predicted decrease in Antarctic near-coastal wind speeds over the remainder of the century will affect flight costs and breeding success and ultimately population trajectories remains to be seen.

The land ice contribution to global mean sea level rise has not yet been predicted using ice sheet and glacier models for the latest set of socio-economic scenarios, nor using coordinated exploration of uncertainties arising from the various computer models involved. Two recent international projects generated a large suite of projections using multiple models, but primarily used previous-generation scenarios and climate models, and could not fully explore known uncertainties. Here we estimate probability distributions for these projections under the new scenarios using statistical emulation of the ice sheet and glacier models. We find that limiting global warming to 1.5 degrees Celsius would halve the land ice contribution to twenty-first-century sea level rise, relative to current emissions pledges. The median decreases from 25 to 13 centimetres sea level equivalent (SLE) by 2100, with glaciers responsible for half the sea level contribution. The projected Antarctic contribution does not show a clear response to the emissions scenario, owing to uncertainties in the competing processes of increasing ice loss and snowfall accumulation in a warming climate. However, under risk-averse (pessimistic) assumptions, Antarctic ice loss could be five times higher, increasing the median land ice contribution to 42 centimetres SLE under current policies and pledges, with the 95th percentile projection exceeding half a metre even under 1.5 degrees Celsius warming. This would severely limit the possibility of mitigating future coastal flooding. Given this large range (between 13 centimetres SLE using the main projections under 1.5 degrees Celsius warming and 42 centimetres SLE using risk-averse projections under current pledges), adaptation planning for twenty-first-century sea level rise must account for a factor-of-three uncertainty in the land ice contribution until climate policies and the Antarctic response are further constrained.

Ozone depletion over Polar Regions is monitored each year by satellite and ground-based instruments. The first signs of healing of the ozone layer linked to the decrease of ozone destructive substances (ODSs) were observed in Antarctica using different metrics (ozone mean values, ozone mass deficit, area of the ozone hole) and simple or sophisticated models. Chemistry climate models predict that climate change will not affect expected ozone recovery over Antarctica but will accelerate recovery in the Arctic due to the possible enhancement of the Brewer Dobson circulation. However, ozone loss observations by SAOZ UV-Vis spectrometers do not show a clear sign of recovery in the latter region. In addition, a record of 38% ozone loss in 2010/2011 and 2019/2020 was estimated. In this study, the vortex-averaged ozone loss in the last three decades will be evaluated for both Polar Regions using the passive ozone tracer of two chemical transport models (REPROBUS and SLIMCAT CTMs) and total ozone observations from SAOZ and satellite observations (IASI/METOP and Multi-Sensor Reanalysis (MSR-2)). The tracer method allows us to determine the evolution of the daily rate of ozone destruction, and the amplitude of the cumulative loss at the end of the winter. The cumulative ozone destruction in the Artic varies between 0-10% in relatively warm winters with short vortex duration to up to 25-38% in colder winters with longer vortex persistence, while in Antarctica it is mostly stable, around 50%. Interannual variability of 10-days average rate will be analyzed and compared between both hemispheres as well as the timing to reach different thresholds of absolute ozone loss values. Finally, linear trend of ozone loss and temperature since 2000 will be estimated in both Polar Regions in order to evaluate possible ozone recovery.

Global targets for area-based conservation and management must move beyond threshold-based targets alone and must account for the quality of such areas. In the Southern Ocean around Antarctica, a region where key biodiversity faces unprecedented risks from climate change and where there is a growing demand to extract resources, a number of marine areas have been afforded enhanced conservation or management measures through two adopted marine protected areas (MPAs). However, evidence suggests that additional high quality areas could benefit from a proposed network of MPAs. Penguins offer a particular opportunity to identify high quality areas because these birds, as highly visible central-place foragers, are considered indicator species whose populations reflect the state of the surrounding marine environment. We compiled a comprehensive dataset of the location of penguin colonies and their associated abundance estimates in Antarctica. We then estimated the at-sea distribution of birds based on information derived from tracking data and through the application of a modified foraging radius approach with a density decay function to identify some of the most important marine areas for chick-rearing adult penguins throughout waters surrounding Antarctica following the Important Bird and Biodiversity Area (IBA) framework. Additionally, we assessed how marine IBAs overlapped with the currently adopted and proposed network of key management areas (primarily MPAs), and how the krill fishery likely overlapped with marine IBAs over the past five decades. We identified 63 marine IBAs throughout Antarctic waters and found that were the proposed MPAs to be adopted, the permanent conservation of high quality areas for penguin species would increase by between 49 and 100% depending on the species. Furthermore, our data show that, despite a generally contracting range of operation by the krill fishery in Antarctica over the past five decades, a consistently disproportionate amount of krill is being harvested within marine IBAs compared to the total area in which the fishery operates. Our results support the designation of the proposed MPA network and offer additional guidance as to where decision-makers should act before further perturbation occurs in the Antarctic marine ecosystem.

Antarctic krill <i>Euphausia superba</i>, a keystone species in the Southern Ocean, is highly relevant for studying effects of climate-related shifts on management systems. Krill provides a key link between primary producers and higher trophic levels and supports the largest regional fishery. Any major perturbation in the krill population would have severe ecological and economic ramifications. We review the literature to determine how climate change, in concert with other environmental changes, alters krill habitat, affects spatial distribution/abundance, and impacts fisheries management. Findings recently reported on the effects of climate change on krill distribution and abundance are inconsistent, however, raising questions regarding methods used to detect changes in density and biomass. One recent study reported a sharp decline in krill densities near their northern limit, accompanied by a poleward contraction in distribution in the Southwest Atlantic sector. Another recent study found no evidence of long-term decline in krill density or biomass and reported no evidence of a poleward shift in distribution. Moreover, with predicted decreases in phytoplankton production, vertical foraging migrations to the seabed may become more frequent, also impacting krill production and harvesting. Potentially cumulative impacts of climate change further compound the management challenge faced by CCAMLR, the organization responsible for conservation of Antarctic marine living resources: to detect changes in the abundance, distribution, and reproductive performance of krill and krill-dependent predator stocks and to respond to such change by adjusting its conservation measures. Based on CCAMLR reports and documents, we review the institutional framework, outline how climate change has been addressed within this organization, and examine the prospects for further advances toward ecosystem risk assessment and an adaptive management system.

Projections of the sea level contribution from the Greenland and Antarctic ice sheets rely on atmospheric and oceanic drivers obtained from climate models. The Earth System Models participating in the Coupled Model Intercomparison Project phase 6 (CMIP6) generally project greater future warming compared with the previous CMIP5 effort. Here we use four CMIP6 models and a selection of CMIP5 models to force multiple ice sheet models as part of the Ice Sheet Model Intercomparison Project for CMIP6 (ISMIP6). We find that the projected sea level contribution at 2100 from the ice sheet model ensemble under the CMIP6 scenarios falls within the CMIP5 range for the Antarctic ice sheet but is significantly increased for Greenland. Warmer atmosphere in CMIP6 models results in higher Greenland mass loss due to surface melt. For Antarctica, CMIP6 forcing is similar to CMIP5 and mass gain from increased snowfall counteracts increased loss due to ocean warming.

Within the framework of the Marine Ecosystem Assessment for the Southern Ocean (MEASO), this paper brings together analyses of recent trends in phytoplankton biomass, primary production and irradiance at the base of the mixed layer in the Southern Ocean and summarises future projections. Satellite observations suggest that phytoplankton biomass in the mixed-layer has increased over the last 20 years in most (but not all) parts of the Southern Ocean, whereas primary production at the base of the mixed-layer has likely decreased over the same period. Different satellite models of primary production (Vertically Generalised versus Carbon Based Production Models) give different patterns and directions of recent change in net primary production (NPP). At present, the satellite record is not long enough to distinguish between trends and climate-related cycles in primary production. Over the next 100 years, Earth system models project increasing NPP in the water column in the MEASO northern and Antarctic zones but decreases in the Subantarctic zone. Low confidence in these projections arises from: (1) the difficulty in mapping supply mechanisms for key nutrients (silicate, iron); and (2) understanding the effects of multiple stressors (including irradiance, nutrients, temperature, pCO₂, pH, grazing) on different species of Antarctic phytoplankton. Notwithstanding these uncertainties, there are likely to be changes to the seasonal patterns of production and the microbial community present over the next 50–100 years and these changes will have ecological consequences across Southern Ocean food-webs, especially on key species such as Antarctic krill and silverfish.

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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.