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      Editorial: thematic issue on Polar and Alpine Microbiology

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          Most cited references31

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          Exploring microbial diversity in Greenland Ice Sheet supraglacial habitats through culturing-dependent and -independent approaches

          The microbiome of Greenland Ice Sheet supraglacial habitats is still underinvestigated, and as a result there is a lack of representative genomes from these environments. In this study, we investigated the supraglacial microbiome through a combination of culturing-dependent and -independent approaches. We explored ice, cryoconite, biofilm, and snow biodiversity to answer: (1) how microbial diversity differs between supraglacial habitats, (2) if obtained bacterial genomes reflect dominant community members, and (3) how culturing versus high throughput sequencing changes our observations of microbial diversity in supraglacial habitats. Genomes acquired through metagenomic sequencing (133 high-quality MAGs) and whole genome sequencing (73 bacterial isolates) were compared to the metagenome assemblies to investigate abundance within the total environmental DNA. Isolates obtained in this study were not dominant taxa in the habitat they were sampled from, in contrast to the obtained MAGs. We demonstrate here the advantages of using metagenome SSU rRNA genes to reflect whole-community diversity. Additionally, we demonstrate a proof-of-concept of the application of in situ culturing in a supraglacial setting. Various culturing-dependent and -independent methods were used to explore microbial diversity on the Greenland Ice Sheet, highlighting the benefits of combining different approaches to capture genomic diversity.
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            Functional microbial ecology in arctic soils: the need for a year-round perspective

            The microbial ecology of arctic and sub-arctic soils is an important aspect of the global carbon cycle, due to the sensitivity of the large soil carbon stocks to ongoing climate warming. These regions are characterized by strong climatic seasonality, but the emphasis of most studies on the short vegetation growing season could potentially limit our ability to predict year-round ecosystem functions. We compiled a database of studies from arctic, subarctic, and boreal environments that include sampling of microbial community and functions outside the growing season. We found that for studies comparing across seasons, in most environments, microbial biomass and community composition vary intra-annually, with the spring thaw period often identified by researchers as the most dynamic time of year. This seasonality of microbial communities will have consequences for predictions of ecosystem function under climate change if it results in: seasonality in process kinetics of microbe-mediated functions; intra-annual variation in the importance of different (a)biotic drivers; and/or potential temporal asynchrony between climate change-related perturbations and their corresponding effects. Future research should focus on (i) sampling throughout the entire year; (ii) linking these multi-season measures of microbial community composition with corresponding functional or physiological measurements to elucidate the temporal dynamics of the links between them; and (iii) identifying dominant biotic and abiotic drivers of intra-annual variation in different ecological contexts. Microbial biomass and community composition vary intra-annually in (sub)arctic environments, which might have consequences for predictions of ecosystem function under climate change.
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              Dynamic trophic shifts in bacterial and eukaryotic communities during the first 30 years of microbial succession following retreat of an Antarctic glacier.

              We examined microbial succession along a glacier forefront in the Antarctic Peninsula representing ∼30 years of deglaciation to contrast bacterial and eukaryotic successional dynamics and abiotic drivers of community assembly using sequencing and soil properties. Microbial communities changed most rapidly early along the chronosequence, and co-occurrence network analysis showed the most complex topology at the earliest stage. Initial microbial communities were dominated by microorganisms derived from the glacial environment, whereas later stages hosted a mixed community of taxa associated with soils. Eukaryotes became increasingly dominated by Cercozoa, particularly Vampyrellidae, indicating a previously unappreciated role for cercozoan predators during early stages of primary succession. Chlorophytes and Charophytes (rather than cyanobacteria) were the dominant primary producers and there was a spatio-temporal sequence in which major groups became abundant succeeding from simple ice Chlorophytes to Ochrophytes and Bryophytes. Time since deglaciation and pH were the main abiotic drivers structuring both bacterial and eukaryotic communities. Determinism was the dominant assembly mechanism for Bacteria, while the balance between stochastic/deterministic processes in eukaryotes varied along the distance from the glacier front. This study provides new insights into the unexpected dynamic changes and interactions across multiple trophic groups during primary succession in a rapidly changing polar ecosystem.
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                Author and article information

                Contributors
                Journal
                FEMS Microbiol Ecol
                FEMS Microbiol Ecol
                femsec
                FEMS Microbiology Ecology
                Oxford University Press
                0168-6496
                1574-6941
                April 2024
                22 March 2024
                22 March 2024
                : 100
                : 4
                : fiae030
                Affiliations
                German Research Centre for Geosciences GFZ , Telegrafenberg A71-359, 14473 Potsdam, Germany
                German Research Centre for Geosciences GFZ , Telegrafenberg A71-359, 14473 Potsdam, Germany
                Université Grenoble Alpes, CNRS, Institute of Geosciences of the Environment IGE , CS 40700, 38 058 Grenoble, France
                University of Ljubljana, Department of Biology, Biotechnical faculty , Jamnikarjeva 101, 1000 Ljubljana, Slovenia
                Rutgers University, Department of Biochemistry and Microbiology , 76 Lipman Drive, New Brunswick, NJ 08901-8525, United States
                Author notes
                Corresponding author. German Research Centre for Geosciences GFZ, Telegrafenberg A71-359, 14473 Potsdam, Germany. E-mail: benning@ 123456gfz-potsdam.de
                Author information
                https://orcid.org/0000-0001-9972-5578
                https://orcid.org/0000-0001-5064-497X
                https://orcid.org/0000-0001-6307-7863
                Article
                fiae030
                10.1093/femsec/fiae030
                10959548
                38518222
                d53a3538-3595-437b-8531-7818b642ecf0
                © The Author(s) 2024. Published by Oxford University Press on behalf of FEMS.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 March 2024
                : 08 March 2024
                : 22 March 2024
                Page count
                Pages: 3
                Categories
                Editorial
                AcademicSubjects/SCI01150

                Microbiology & Virology
                Microbiology & Virology

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