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Terrestrial vegetation communities across Antarctica are characteristically sparse, presenting a challenge for mapping their occurrence using remote sensing at the continent scale. At present there is no continent-wide baseline record of Antarctic vegetation, and large-scale area estimates remain unquantified. With local vegetation distribution shifts now apparent and further predicted in response to environmental change across Antarctica, it is critical to establish a baseline to document these changes. Here we present a 10 m-resolution map of photosynthetic life in terrestrial and cryospheric habitats across the entire Antarctic continent, maritime archipelagos and islands south of 60° S. Using Sentinel-2 imagery (2017–2023) and spectral indices, we detected terrestrial green vegetation (vascular plants, bryophytes, green algae) and lichens across ice-free areas, and cryospheric green snow algae across coastal snowpacks. The detected vegetation occupies a total area of 44.2 km2, with over half contained in the South Shetland Islands, altogether contributing just 0.12% of the total ice-free area included in the analysis. Due to methodological constraints, dark-coloured lichens and cyanobacterial mats were excluded from the study. This vegetation map improves the geospatial data available for vegetation across Antarctica, and provides a tool for future conservation planning and large-scale biogeographic assessments.

During February–March of the austral summers of 2013/14 and 2014/2015, fieldwork was performed on Half Moon Island, South Shetland Archipelago, Antarctica, to evaluate the distribution and abundance of mosses and lichens, as well as to describe and map the plant communities there. The quadrat (20 × 20 cm) sampling method was employed in a phytosociological study that aimed to describe these communities. The area was mapped using an Astech Promark II® DGPS, yielding sub-metric precision after post-processing with software. The number of species totalled 38 bryophytes, 59 lichens, only one flowering plant (Deschampsia antarctica Desv.), and two macroscopic terrestrial algae. Five types of plant communities were identified on the island, as follows: (1) fruticose lichen and moss cushion, (2) moss carpet, (3) muscicolous lichen, (4) crustose lichen and (5) moss turf.

Usnea aurantiaco-atra is the most widespread flora in Fildes Peninsula. There are two growth types of U. aurantiaco-atra: the erect form on rocks and the prostrate form associated with mosses. Phylogenetic analysis showed that individuals of the two growth forms share genotypes. Moreover, haploid disequilibrium testing indicated no significant genetic difference for the two growth forms when fungal and algal internal transcribed spacer rDNA were treated as two alleles of one lichen individual. The two growth forms of U. aurantiaco-atra appear to reflect different stages of lichen–moss community succession. A mode is proposed for demonstrating the occurrence of this succession.

On the Antarctic Peninsula, lichens are the most diverse botanical component of the terrestrial ecosystem. However, detailed information on the distribution of lichens on the Antarctic Peninsula region is scarce, and the data available exhibit significant heterogeneity in sampling frequency and effort. Satellite remote sensing, in particular the use of the Normalized Difference Vegetation Index (NDVI), has facilitated determination of vegetation richness and cover distribution in some remote and otherwise inaccessible environments. However, it is known that using NDVI for the detection of vegetation can overlook the presence of lichens even if their land cover is extensive. We tested the use of known spectra of lichens in a matched filtering technique for the detection and mapping of lichen-covered land from remote sensing imagery on the Antarctic Peninsula, using data on lichen presence collected by citizen scientists and other non-specialists as ground truthing. Our results confirm that the use of this approach allows for the detection of lichen flora on the Antarctic Peninsula, showing an improvement over the use of NDVI alone for the mapping of flora in this area. Keywords: Antarctica; NDVI; matched filtering; Landsat; remote sensing.

Winter climate and snow cover are the important drivers of plant community development in polar regions. However, the impacts of changing winter climate and associated changes in snow regime have received much less attention than changes during summer. Here, we synthesize the results from studies on the impacts of extreme winter weather events on polar heathland and lichen communities. Dwarf shrubs, mosses and soil arthropods were negatively impacted by extreme warming events while lichens showed variable responses to changes in extreme winter weather events. Snow mould formation underneath the snow may contribute to spatial heterogeneity in plant growth, arthropod communities and carbon cycling. Winter snow cover and depth will drive the reported impacts of winter climate change and add to spatial patterns in vegetation heterogeneity. The challenges ahead lie in obtaining better predictions on the snow patterns across the landscape and how these will be altered due to winter climate change.

It is shown by use of a newly discovered, old photo of the missing type that Siphulina orphnina (Hue) C. W. Dodge is identical with Pannaria caespitosa P. M. Jorg. The new combination Pannaria orphnina (Hue) R M. Jorg. is made, and the name neotypitied. Parmeliella austroshetlandica Sochting & Ovstedal is shown to be a species in the small subantarctic genus Peltularia R. Sant. (Coccocarpiaceae), and is transferred to that genus.

The taxonomic listing given in Lichens of Antarctica and South Georgia (Øvstedal & Lewis Smith 2001) has been updated. 17 additional taxa of lichenised fungi are described, including several nomenclatural changes. 14 of these are considered as new records for the Antarctic and one is new to South Georgia. One is described as new to science.

Much evidence suggests that life originated in hydrothermal habitats, and for much of the time since the origin of cyanobacteria (at least 2·5 Ga ago) and of eukaryotic algae (at least 2·1 Ga ago) the average sea surface and land surface temperatures were higher than they are today. However, there have been at least four significant glacial episodes prior to the Pleistocene glaciations. Two of these (approx. 2·1 and 0·7 Ga ago) may have involved a ‘Snowball Earth’ with a very great impact on the algae (sensu lato) of the time (cyanobacteria, Chlorophyta and Rhodophyta) and especially those that were adapted to warm habitats. By contrast, it is possible that heterokont, dinophyte and haptophyte phototrophs only evolved after the Carboniferous–Permian ice age (approx. 250 Ma ago) and so did not encounter low (≤5 °C) sea surface temperatures until the Antarctic cooled some 15 Ma ago. Despite this, many of the dominant macroalgae in cooler seas today are (heterokont) brown algae, and many laminarians cannot reproduce at temperatures above 18–25 °C. By contrast to plants in the aerial environment, photosynthetic structures in water are at essentially the same temperature as the fluid medium. The impact of low temperatures on photosynthesis by marine macrophytes is predicted to favour diffusive CO2 entry rather than a CO2‐concentrating mechanism. Some evidence favours this suggestion, but more data are needed.

The effects of UV-B exclusion and enhancement of solar radiation on photosynthesis of the two phanerogams which occur in the maritime Antarctic, Deschampsia antarctica and Colobanthus quitensis, and the moss Sanionia uncinats were investigated. Data on air temperature and solar radiation illustrate a drastic seasonal variation. Daily O3 column mean values and UV-B measured at ground level document the occurrence of the O3“hole” in the spring of 1997, with a concomitant increase in UV-B. The grass, D. antarctica, exhibited a broad temperature optimum for photosynthesis between 10–25°C while photosynthesis did not saturate even at high irradiance. The high water use efficiencies measured in the grass may be one of the features explaining the presence of this species in the maritime Antarctic. The net photosynthesis response to intercellular CO2 (A/ci) for D. antarctica was typical of a C3 plant. Exposure to a biologically effective UV-B irradiance of 0.74 W M-2 did not result in any significant change in either the maximum rate of photosynthesis at saturating CO2 and light, or in the initial carboxylation efficiency of Rubisco. (Vc,max). Furthermore while ambient (or enhanced) solar UV-B did not affect photochemical yield, measured in the field, of C. quitensis and D. antarctica, UV-B enhancement did affect negatively photochemical yield in S. uncinata. In D. antarctica plants, exposure to UV-B at low irradiances elicited increased flavonoid synthesis. The observed effects of UV-B enhancement on the moss (decreased photochemical yield) and the grass (increase in flavonoids) require further, separate investigation.

A new species of Parmelia (lichenized Ascomycotina) from the Antarctic. Parmelia lindsayana Ovstedal & Elix from Signy Island (South Orkney Islands) is described as new. This species resembles P. protosulcata Hale and P. cunninghamii Crombie, but differs in morphological details and in containing usnic, alpha-collatolic and alectoronic acids.

A new muscicolous lichen species, Caloplaca lewis-smithii Søchting & Øvst., is described from Victoria Land, continental Antarctica. It is characterized by a grey to blackish brown microlobate thallus and a blackish apothecial disk with a white pruinose thalline margin.

Many invertebrates show flexibility in their life cycles and are likely to respond to changes in climate as they have in the past. However, changes in temperature and photoperiod may disturb the life cycles of some existing polar invertebrates while continuing to constrain the polewards migration of more temperate species. Higher plants are likely to have higher productivity as temperatures and atmospheric CO2 levels increase but this productivity will be reduced by exposure to increasing UV-B radiation. Higher plants migrate more slowly than the rate at which climate is predicted to change and many species will be trapped in supra-optimal climates. Both mosses and lichens can migrate faster than higher plants, propagules of non-polar species already reaching the Antarctic, but they have fewer mechanisms of responding to changing environments. Polar vegetation and ecosystems provide feedback to the climate system: positive feedbacks are associated with decreases in reflectivity and increased carbon emissions from warm ing soils. In the Antarctic, feedback and responses to environmental change will be smaller than in the Arctic because of the less responsive cryptogams which dominate the Antarctic, the paucity of Antarctic soils, and geographical barriers to plant and invertebrate migrations.

Laboratory measurements show that lichens are extremely tolerant of freezing stress and of low-temperature exposure. Metabolic activity recovered quickly after severe and extended cold treatment. Experimental results demonstrate also that CO2 exchange is already active at around −20°C. The psychrophilic character of polar lichen species is demonstrated by optimum temperatures for net photosynthesis between 0 and 15°C. In situ measurements show that lichens begin photosynthesizing below 0°C if the dry thalli receive fresh snow. The lowest temperature measured in active lichens was −17°C at a continental Antarctic site. The fine structure and the hydration state of photobiont and mycobiont cells were studied by low-temperature scanning electron microscopy (LTSEM) of frozen hydrated specimens. Water potentials of the frozen system are in the range of or even higher than those allowing dry lichens to start photosynthesis by water vapor uptake at +10°C. The great success of lichens in polar and high alpine regions gives evidence of their physiological adaptation to low temperatures. In general lichens are able to persist through glacial periods, but extended snow cover and glaciation are limiting factors.

A new araphid diatom genus, Synedropsis Hasle, Medlin et Syvertsen, is described from sea ice. The generitype, Synedropsis hyperborea (Grunow) Hasle, Medlin et Syvertsen from the Arctic, was first described as a species of Synedra, as was the antarctic Synedropsis fragilis (Manguin) Hasle, Syvertsen et Medlin. A second antarctic species of Synedropsis is a new combination of Cymatosira laevis Heiden in Heiden & Kolbe. In addition four new taxa, S. hyperboreoides Hasle, Syvertsen et Medlin, S. recta Hasle, Medlin et Syvertsen, S. lata Hasle, Medlin et Syvertsen and S. lata var. angustata Hasle, Medlin et Syvertsen are described from the Antarctic. The valve wall is laminar with uniseriate, often poorly developed striae and a wide sternum. Each valve possesses apical fields composed of slits. A labiate process is positioned near one apical slit field. The valve outline for most species exhibits considerable stadial variation. The girdle has several bands, most with one row of poroids close to the pars interior. Thus Synedropsis is closely related to the marine Fragilaria striatula Lyngbye except in the structure of the apical fields and the number of bands. Species observed in uncleaned material appeared in stellate or, more seldom, ribbon-shaped colonies. Synedropsis hyperborea is a common epiphyte on the ice-associated Melosira arctica Dickie in the Arctic. The antarctic species were found mainly in the bottom ice community, S. fragilis as an epiphyte on other diatoms.

The bipolar foliose lichen Solorina spongiosa (Sm.) Anzi is reported from James Ross Island, Antarctica, where it grows on moss. This is only the third known occurrence of this lichen from the Southern Hemisphere, the other localities being in Tierra del Fuego and New Zealand. Its morphology resembles that of the New Zealand population and arctic-alpine populations from the Northern Hemisphere, although there are some differences in apothecial and spore size. As elsewhere, it occupies base-rich habitats colonized by predominantly calcicolous mosses and lichens.

Six species of Stereocaulon and one unnamed taxon (close to S. glabrum) are reported from South Georgia, the maritime Antarctic islands and Antarctic Peninsula. S. caespitosum is new to the western sub-Antarctic. Variations in morphology and secondary chemistry are provided, and the ecology and geographical distribution in the sub-Antarctic and Antarctic biomes are given for each taxon.

Some Nitzschia and closely related species have been examined in the light and electron microscopes from fast ice samples in the Arctic and Antarctic. Nitzschia neofrigida, forming arborescent colonies, and Nitzschia promare, forming loose ribbon colonies, are described as new species, both probably included in the distribution of other similar species. A new combination, Auricula compacta, represents the first report of this genus from ice samples. Colony formation is reported for the first time in Nitzschia arctica and Nitzschia taeniiformis. No biopolar species were found and several reports of Arctic species in Antarctic ice samples have been refuted.