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Competition and niche separation of pelagic bacteria in freshwater habitats
Summary Freshwater bacterioplankton assemblages are composed of sympatric populations that can be delineated, for example, by ribosomal RNA gene relatedness and that differ in key ecophysiological properties. They may be free‐living or attached, specialized for particular concentrations or subsets o...
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Published in: | Environmental microbiology 2017-06, Vol.19 (6), p.2133-2150 |
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Freshwater bacterioplankton assemblages are composed of sympatric populations that can be delineated, for example, by ribosomal RNA gene relatedness and that differ in key ecophysiological properties. They may be free‐living or attached, specialized for particular concentrations or subsets of substrates, or invest a variable amount of their resources in defence traits against protistan predators and viruses. Some may be motile and tactic whereas others are not, with far‐reaching implications for their respective life styles and niche partitioning. The co‐occurrence of competitors with overlapping growth requirements has profound consequences for the stability of community functions; it can to some extent be explained by habitat factors such as the microscale complexity and spatiotemporal variability of the lacustrine environments. On the other hand, the composition and diversity of freshwater microbial assemblages also reflects non‐equilibrium states, dispersal and the stochasticity of community assembly processes. This review synoptically discusses the competition and niche separation of heterotrophic bacterial populations (defined at various levels of phylogenetic resolution) in the pelagic zone of inland surface waters from a variety of angles, focusing on habitat heterogeneity and the resulting biogeographic distribution patterns, the ecophysiological adaptations to the substrate field and the interactions of prokaryotes with predators and viruses. |
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Freshwater bacterioplankton assemblages are composed of sympatric populations that can be delineated, for example, by ribosomal RNA gene relatedness and that differ in key ecophysiological properties. They may be free‐living or attached, specialized for particular concentrations or subsets of substrates, or invest a variable amount of their resources in defence traits against protistan predators and viruses. Some may be motile and tactic whereas others are not, with far‐reaching implications for their respective life styles and niche partitioning. The co‐occurrence of competitors with overlapping growth requirements has profound consequences for the stability of community functions; it can to some extent be explained by habitat factors such as the microscale complexity and spatiotemporal variability of the lacustrine environments. On the other hand, the composition and diversity of freshwater microbial assemblages also reflects non‐equilibrium states, dispersal and the stochasticity of community assembly processes. This review synoptically discusses the competition and niche separation of heterotrophic bacterial populations (defined at various levels of phylogenetic resolution) in the pelagic zone of inland surface waters from a variety of angles, focusing on habitat heterogeneity and the resulting biogeographic distribution patterns, the ecophysiological adaptations to the substrate field and the interactions of prokaryotes with predators and viruses.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.13742</identifier><identifier>PMID: 28370850</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adaptation ; Adaptation, Physiological - physiology ; Aquatic habitats ; Aquatic Organisms - metabolism ; Aquatic Organisms - microbiology ; Bacteria ; Bacteria - genetics ; Bacteria - metabolism ; Bacterioplankton ; Communities ; Competition ; Dispersal ; Distribution patterns ; Ecosystem ; Fresh Water - microbiology ; Freshwater environments ; Heterogeneity ; Host-Parasite Interactions - physiology ; Microorganisms ; Niche overlap ; Nutrient requirements ; Pelagic zone ; Phylogeny ; Populations ; Predators ; Prokaryotes ; Resource partitioning ; Ribonucleic acid ; RNA ; rRNA ; Separation ; Stochasticity ; Substrates ; Surface water ; Sympatric populations ; Viruses</subject><ispartof>Environmental microbiology, 2017-06, Vol.19 (6), p.2133-2150</ispartof><rights>2017 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><rights>2017 Society for Applied Microbiology and John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4122-13bec897f60b5f24a8ba3d75b2fb220a9286b3a7d66f122f698b597cde0c6d063</citedby><cites>FETCH-LOGICAL-c4122-13bec897f60b5f24a8ba3d75b2fb220a9286b3a7d66f122f698b597cde0c6d063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28370850$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pernthaler, Jakob</creatorcontrib><title>Competition and niche separation of pelagic bacteria in freshwater habitats</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary
Freshwater bacterioplankton assemblages are composed of sympatric populations that can be delineated, for example, by ribosomal RNA gene relatedness and that differ in key ecophysiological properties. They may be free‐living or attached, specialized for particular concentrations or subsets of substrates, or invest a variable amount of their resources in defence traits against protistan predators and viruses. Some may be motile and tactic whereas others are not, with far‐reaching implications for their respective life styles and niche partitioning. The co‐occurrence of competitors with overlapping growth requirements has profound consequences for the stability of community functions; it can to some extent be explained by habitat factors such as the microscale complexity and spatiotemporal variability of the lacustrine environments. On the other hand, the composition and diversity of freshwater microbial assemblages also reflects non‐equilibrium states, dispersal and the stochasticity of community assembly processes. This review synoptically discusses the competition and niche separation of heterotrophic bacterial populations (defined at various levels of phylogenetic resolution) in the pelagic zone of inland surface waters from a variety of angles, focusing on habitat heterogeneity and the resulting biogeographic distribution patterns, the ecophysiological adaptations to the substrate field and the interactions of prokaryotes with predators and viruses.</description><subject>Adaptation</subject><subject>Adaptation, Physiological - physiology</subject><subject>Aquatic habitats</subject><subject>Aquatic Organisms - metabolism</subject><subject>Aquatic Organisms - microbiology</subject><subject>Bacteria</subject><subject>Bacteria - genetics</subject><subject>Bacteria - metabolism</subject><subject>Bacterioplankton</subject><subject>Communities</subject><subject>Competition</subject><subject>Dispersal</subject><subject>Distribution patterns</subject><subject>Ecosystem</subject><subject>Fresh Water - microbiology</subject><subject>Freshwater environments</subject><subject>Heterogeneity</subject><subject>Host-Parasite Interactions - physiology</subject><subject>Microorganisms</subject><subject>Niche overlap</subject><subject>Nutrient requirements</subject><subject>Pelagic zone</subject><subject>Phylogeny</subject><subject>Populations</subject><subject>Predators</subject><subject>Prokaryotes</subject><subject>Resource partitioning</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>rRNA</subject><subject>Separation</subject><subject>Stochasticity</subject><subject>Substrates</subject><subject>Surface water</subject><subject>Sympatric populations</subject><subject>Viruses</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkMFPwyAUh4nROJ2evRkSL17qgJZCj2aZujjjRc8EKDiWrq3QZtl_L1vnDl7k8ngv3_vl5QPgBqMHHN8EZzlJSEFim7KMnICL4-T0-MdkBC5DWCGEWcrQORgRHiun6AK8Tpt1azrXuaaGsi5h7fTSwGBa6eV-2FjYmkp-OQ2V1J3xTkJXQ-tNWG5k7OFSKtfJLlyBMyurYK4PdQw-n2Yf05dk8f48nz4uEp1hQhKcKqN5wWyOFLUkk1zJtGRUEasIQbIgPFepZGWe28jbvOCKFkyXBum8RHk6BvdDbuub796ETqxd0KaqZG2aPgjMeYYZSimP6N0fdNX0vo7XCRy9YEyLgkZqMlDaNyF4Y0Xr3Vr6rcBI7DyLnUmxsyr2nuPG7SG3V2tTHvlfsRGgA7Bxldn-lydmb_Mh-Aexb4YY</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Pernthaler, Jakob</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QH</scope><scope>7QL</scope><scope>7ST</scope><scope>7T7</scope><scope>7TN</scope><scope>7U9</scope><scope>7UA</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>201706</creationdate><title>Competition and niche separation of pelagic bacteria in freshwater habitats</title><author>Pernthaler, Jakob</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4122-13bec897f60b5f24a8ba3d75b2fb220a9286b3a7d66f122f698b597cde0c6d063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adaptation</topic><topic>Adaptation, Physiological - physiology</topic><topic>Aquatic habitats</topic><topic>Aquatic Organisms - metabolism</topic><topic>Aquatic Organisms - microbiology</topic><topic>Bacteria</topic><topic>Bacteria - genetics</topic><topic>Bacteria - metabolism</topic><topic>Bacterioplankton</topic><topic>Communities</topic><topic>Competition</topic><topic>Dispersal</topic><topic>Distribution patterns</topic><topic>Ecosystem</topic><topic>Fresh Water - microbiology</topic><topic>Freshwater environments</topic><topic>Heterogeneity</topic><topic>Host-Parasite Interactions - physiology</topic><topic>Microorganisms</topic><topic>Niche overlap</topic><topic>Nutrient requirements</topic><topic>Pelagic zone</topic><topic>Phylogeny</topic><topic>Populations</topic><topic>Predators</topic><topic>Prokaryotes</topic><topic>Resource partitioning</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>rRNA</topic><topic>Separation</topic><topic>Stochasticity</topic><topic>Substrates</topic><topic>Surface water</topic><topic>Sympatric populations</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pernthaler, Jakob</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pernthaler, Jakob</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Competition and niche separation of pelagic bacteria in freshwater habitats</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2017-06</date><risdate>2017</risdate><volume>19</volume><issue>6</issue><spage>2133</spage><epage>2150</epage><pages>2133-2150</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>Summary
Freshwater bacterioplankton assemblages are composed of sympatric populations that can be delineated, for example, by ribosomal RNA gene relatedness and that differ in key ecophysiological properties. They may be free‐living or attached, specialized for particular concentrations or subsets of substrates, or invest a variable amount of their resources in defence traits against protistan predators and viruses. Some may be motile and tactic whereas others are not, with far‐reaching implications for their respective life styles and niche partitioning. The co‐occurrence of competitors with overlapping growth requirements has profound consequences for the stability of community functions; it can to some extent be explained by habitat factors such as the microscale complexity and spatiotemporal variability of the lacustrine environments. On the other hand, the composition and diversity of freshwater microbial assemblages also reflects non‐equilibrium states, dispersal and the stochasticity of community assembly processes. This review synoptically discusses the competition and niche separation of heterotrophic bacterial populations (defined at various levels of phylogenetic resolution) in the pelagic zone of inland surface waters from a variety of angles, focusing on habitat heterogeneity and the resulting biogeographic distribution patterns, the ecophysiological adaptations to the substrate field and the interactions of prokaryotes with predators and viruses.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28370850</pmid><doi>10.1111/1462-2920.13742</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation Adaptation, Physiological - physiology Aquatic habitats Aquatic Organisms - metabolism Aquatic Organisms - microbiology Bacteria Bacteria - genetics Bacteria - metabolism Bacterioplankton Communities Competition Dispersal Distribution patterns Ecosystem Fresh Water - microbiology Freshwater environments Heterogeneity Host-Parasite Interactions - physiology Microorganisms Niche overlap Nutrient requirements Pelagic zone Phylogeny Populations Predators Prokaryotes Resource partitioning Ribonucleic acid RNA rRNA Separation Stochasticity Substrates Surface water Sympatric populations Viruses |
title | Competition and niche separation of pelagic bacteria in freshwater habitats |
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