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Incomplete species inventories for Antarctica represent a key challenge for comprehensive ecological research and conservation in the region. Additionally, data required to understand population dynamics, rates of evolution, spatial ranges, functional traits, physiological tolerances and species interactions, all of which are fundamental to disentangle the different functional elements of Antarctic biodiversity, are mostly missing. However, much of the fauna, flora and microbiota in the emerged ice-free land of the continent have an uncertain presence and/or unresolved status, with entire biodiversity compendia of prokaryotic groups (e.g. bacteria) being missing. All the available biodiversity information requires consolidation, cross-validation, re-assessment and steady systematic inclusion in order to create a robust catalogue of biodiversity for the continent.We compiled, completed and revised eukaryotic species inventories present in terrestrial and freshwater ecosystems in Antarctica in a new living database: terrANTALife (version 1.0). The database includes the first integration in a compendium for many groups of eukaryotic microorganisms. We also introduce a first catalogue of amplicon sequence variants (ASVs) of prokaryotic biodiversity. Available compendia and literature to date were searched for Antarctic terrestrial and freshwater species, integrated, taxonomically harmonised and curated by experts to create comprehensive checklists of Antarctic organisms. The final inventories comprises 470 animal species (including vertebrates, free-living invertebrates and parasites), 306 plants (including all Viridiplantae: embryophytes and green algae), 997 fungal species and 434 protists (sensu lato). We also provide a first account for many groups of microorganisms, including non-lichenised fungi and multiple groups of eukaryotic unicellular species (Stramenophila, Alveolata and Rhizaria (SAR), Chromists and Amoeba), jointly referred to as "protists". In addition, we identify 1753 bacterial (obtained from 348117 ASVs) and 34 archaeal genera (from 1848 ASVs), as well as, at least, 14 virus families. We formulate a basic tree of life in Antarctica with the main lineages listed in the region and their “known-accepted-species” numbers.

Snowmelt in the Antarctic Peninsula region has increased significantly in recent decades, leading to greater liquid water availability across a more expansive area. As a consequence, changes in the biological activity within wet Antarctic snow require consideration if we are to better understand terrestrial carbon cycling on Earth's coldest continent. This paper therefore examines the relationship between microbial communities and the chemical and physical environment of wet snow habitats on Livingston Island of the maritime Antarctic. In so doing, we reveal a strong reduction in bacterial diversity and autotrophic biomass within a short (<1 km) distance from the coast. Coastal snowpacks, fertilized by greater amounts of nutrients from rock debris and marine fauna, develop obvious, pigmented snow algal communities that control the absorption of visible light to a far greater extent than with the inland glacial snowpacks. Absorption by carotenoid pigments is most influential at the surface, while chlorophyll is most influential beneath it. The coastal snowpacks also indicate higher concentrations of dissolved inorganic carbon and CO2 in interstitial air, as well as a close relationship between chlorophyll and dissolved organic carbon (DOC). As a consequence, the DOC resource available in coastal snow can support a more diverse bacterial community that includes microorganisms from a range of nearby terrestrial and marine habitats. Therefore, since further expansion of the melt zone will influence glacial snowpacks more than coastal ones, care must be taken when considering the types of communities that may be expected to evolve there.

The continental shelf of Antarctica harbours rich suspension-feeding macroinvertebrate communities that are continuously exposed to large populations of free-living microbes. To avoid settlement or fouling by undesirable microorganisms that could cause infection or collapse filter-feeding systems, these macroinvertebrates might regulate the epibiotic microbial mat through chemical interactions. In Antarctic chemical ecology, the antibacterial roles of natural products remain mostly unknown. A necessary first step is to identify organisms that produce compounds with potential ecological relevance. For that reason, we tested the crude organic extracts of 116 taxa of Antarctic benthic organisms for antibacterial activity against a panel of seven strains of marine bacteria. Nine out of 11 phyla tested had antibacterial properties. However, inhibitory activity was quite selective and species-specific. These patterns suggest that Antarctic benthic organisms may produce diverse bioactive metabolites with different antibacterial activities or, alternatively, those contrasting profiles may be shaped by environmental and biological interactions acting at a small spatial scale. The reasons of such selectivity remain to be further investigated and may contribute to the identification of bioactive compounds with pharmaceutical applications.

Recent studies have concluded that different water bodies in the ocean can contain different microbial communities. The goal of the present study was to determine if biogeographic patterns are present for aquatic microbes in waters which meet around the South Shetland Islands(SSI), Antarctica. Prokaryotic and eukaryotic marine microbial communities were monitored during the 2007 austral summer by use of polymerase chain reaction (PCR) and denaturing gradientgel electrophoresis (DGGE) of small subunit ribosomal DNA. Hydrographic properties, nutrients and chlorophyll a were also measured. There was an onshore to offshore gradient in temperature, salinity and iron concentration and a unimodal distribution of chlorophyll a concentration in rela-tion to the middle of this gradient that occurred near the SSI. The differences in microbial community structure among stations in the studied area were correlated with both geographical distance and environmental factors. For eukaryotes, the correlation was strongest for environment, where as it was strongest for geographical distance for the prokaryotes. Eukaryotic and prokaryotic community structures were highly correlated. Surface water from the Weddell Sea had a different community of eukaryotes than the water in the Antarctic Circumpolar Current in the Drake Passage, whereas the prokaryotic community was not significantly different. The area close to theSSI where the 2 water types mix had the highest chlorophyll concentration and significantly dif-ferent communities of eukaryotes and prokaryotes from both of the inflowing water types. These results suggest that the prokaryote community structure was more affected by productivity thanby environmental variables. KEY WORDS: Microbial biogeography. Microbial community. Natural iron enrichment. Southern Ocean.

Antarctic bacteria producing extracellular lipolytic enzymes with activity at low temperature were isolated, and the most promising strain, named G, was identified as a Psychrobacter species based on 16S rDNA sequence alignment. The genomic DNA of this bacterium was used to construct its plasmid genomic library into pUC118 plasmid vectors, and to screen the cold-active lipolytic enzyme genes. Two genes encoding for cold-active lipolytic enzymes, Lip-1452 (with an open reading frame of 1452 bp in length) and Lip-948 (with an open reading frame of 948 bp in length), were screened. The primary structure of the two lipases deduced from the nucleotide sequence showed a consensus pentapeptide containing the active serine (Lip-1452, GDSAG, and Lip-948, GNSMG) and a conserved His-Gly dipeptide in the N-terminal part of the enzyme. Protein sequence alignment and conserved regions analysis indicated that the two lipases probably belonged to family IV and family V of the bacterial lipolytic enzymes, respectively. The upstream and downstream sequences of the two lipolytic lipases were also obtained. The two lipase genes were cloned into the expression vector pCold III and integrated into Escherichia coli BL21 (DE3). The functional expression of both lipase genes by E. coli BL21 (DE3) cells was observed as the formation of clear haloes around colonies on a 1% (vol/vol) tributyrin plate upon induction with isopropyl-b-Dthiogalactopyranoside at 5°C. A lipase activity assay showed that the specific activity of the pCold III+Lip-948 expression system was up to 3.7 U ml-1, whereas that of pCold III+Lip-1452 was very low.