Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert
Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and...
Ausführliche Beschreibung
Autor*in: |
Guang, Song [verfasserIn] |
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Englisch |
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2023 |
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© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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Übergeordnetes Werk: |
Enthalten in: Plant and soil - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1948, 490(2023), 1-2 vom: 18. Mai, Seite 217-237 |
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Übergeordnetes Werk: |
volume:490 ; year:2023 ; number:1-2 ; day:18 ; month:05 ; pages:217-237 |
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DOI / URN: |
10.1007/s11104-023-06071-x |
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SPR053220730 |
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520 | |a Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. | ||
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10.1007/s11104-023-06071-x doi (DE-627)SPR053220730 (SPR)s11104-023-06071-x-e DE-627 ger DE-627 rakwb eng Guang, Song verfasserin aut Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. Biocrusts (dpeaa)DE-He213 Bacterial community composition (dpeaa)DE-He213 Cooccurrence network (dpeaa)DE-He213 Complexity and stability (dpeaa)DE-He213 Environmental driver (dpeaa)DE-He213 Ying, Zheng aut Haotian, Yang aut Xinrong, Li aut Enthalten in Plant and soil Dordrecht [u.a.] : Springer Science + Business Media B.V, 1948 490(2023), 1-2 vom: 18. Mai, Seite 217-237 (DE-627)270934979 (DE-600)1478535-3 1573-5036 nnns volume:490 year:2023 number:1-2 day:18 month:05 pages:217-237 https://dx.doi.org/10.1007/s11104-023-06071-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 490 2023 1-2 18 05 217-237 |
spelling |
10.1007/s11104-023-06071-x doi (DE-627)SPR053220730 (SPR)s11104-023-06071-x-e DE-627 ger DE-627 rakwb eng Guang, Song verfasserin aut Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. Biocrusts (dpeaa)DE-He213 Bacterial community composition (dpeaa)DE-He213 Cooccurrence network (dpeaa)DE-He213 Complexity and stability (dpeaa)DE-He213 Environmental driver (dpeaa)DE-He213 Ying, Zheng aut Haotian, Yang aut Xinrong, Li aut Enthalten in Plant and soil Dordrecht [u.a.] : Springer Science + Business Media B.V, 1948 490(2023), 1-2 vom: 18. Mai, Seite 217-237 (DE-627)270934979 (DE-600)1478535-3 1573-5036 nnns volume:490 year:2023 number:1-2 day:18 month:05 pages:217-237 https://dx.doi.org/10.1007/s11104-023-06071-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 490 2023 1-2 18 05 217-237 |
allfields_unstemmed |
10.1007/s11104-023-06071-x doi (DE-627)SPR053220730 (SPR)s11104-023-06071-x-e DE-627 ger DE-627 rakwb eng Guang, Song verfasserin aut Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. Biocrusts (dpeaa)DE-He213 Bacterial community composition (dpeaa)DE-He213 Cooccurrence network (dpeaa)DE-He213 Complexity and stability (dpeaa)DE-He213 Environmental driver (dpeaa)DE-He213 Ying, Zheng aut Haotian, Yang aut Xinrong, Li aut Enthalten in Plant and soil Dordrecht [u.a.] : Springer Science + Business Media B.V, 1948 490(2023), 1-2 vom: 18. Mai, Seite 217-237 (DE-627)270934979 (DE-600)1478535-3 1573-5036 nnns volume:490 year:2023 number:1-2 day:18 month:05 pages:217-237 https://dx.doi.org/10.1007/s11104-023-06071-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 490 2023 1-2 18 05 217-237 |
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10.1007/s11104-023-06071-x doi (DE-627)SPR053220730 (SPR)s11104-023-06071-x-e DE-627 ger DE-627 rakwb eng Guang, Song verfasserin aut Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. Biocrusts (dpeaa)DE-He213 Bacterial community composition (dpeaa)DE-He213 Cooccurrence network (dpeaa)DE-He213 Complexity and stability (dpeaa)DE-He213 Environmental driver (dpeaa)DE-He213 Ying, Zheng aut Haotian, Yang aut Xinrong, Li aut Enthalten in Plant and soil Dordrecht [u.a.] : Springer Science + Business Media B.V, 1948 490(2023), 1-2 vom: 18. Mai, Seite 217-237 (DE-627)270934979 (DE-600)1478535-3 1573-5036 nnns volume:490 year:2023 number:1-2 day:18 month:05 pages:217-237 https://dx.doi.org/10.1007/s11104-023-06071-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 490 2023 1-2 18 05 217-237 |
allfieldsSound |
10.1007/s11104-023-06071-x doi (DE-627)SPR053220730 (SPR)s11104-023-06071-x-e DE-627 ger DE-627 rakwb eng Guang, Song verfasserin aut Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. Biocrusts (dpeaa)DE-He213 Bacterial community composition (dpeaa)DE-He213 Cooccurrence network (dpeaa)DE-He213 Complexity and stability (dpeaa)DE-He213 Environmental driver (dpeaa)DE-He213 Ying, Zheng aut Haotian, Yang aut Xinrong, Li aut Enthalten in Plant and soil Dordrecht [u.a.] : Springer Science + Business Media B.V, 1948 490(2023), 1-2 vom: 18. Mai, Seite 217-237 (DE-627)270934979 (DE-600)1478535-3 1573-5036 nnns volume:490 year:2023 number:1-2 day:18 month:05 pages:217-237 https://dx.doi.org/10.1007/s11104-023-06071-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 490 2023 1-2 18 05 217-237 |
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author |
Guang, Song |
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Guang, Song misc Biocrusts misc Bacterial community composition misc Cooccurrence network misc Complexity and stability misc Environmental driver Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert |
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Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert Biocrusts (dpeaa)DE-He213 Bacterial community composition (dpeaa)DE-He213 Cooccurrence network (dpeaa)DE-He213 Complexity and stability (dpeaa)DE-He213 Environmental driver (dpeaa)DE-He213 |
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misc Biocrusts misc Bacterial community composition misc Cooccurrence network misc Complexity and stability misc Environmental driver |
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Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert |
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Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert |
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Guang, Song Ying, Zheng Haotian, Yang Xinrong, Li |
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biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the tengger desert |
title_auth |
Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert |
abstract |
Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
abstractGer |
Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
abstract_unstemmed |
Background and Aims Biocrusts cover approximately 30% of the global dryland surface area, constituting a crucial atmosphere–soil interface. Bacteria living at this interface participate in almost all biogeochemical cycling processes that may profoundly alter soil and ecosystem multifunctionality and speed up ecosystem restoration. However, the successional dynamics of bacterial communities in both biocrusts and subsoil remain largely unclear. Methods This study used α and β diversity assessments and molecular ecological networks to reveal the bacterial community succession in biocrusts and subsoil along a 65-year succession sequence (a succession of biocrust types ranging from cyanobacteria to lichens to mosses) on the southeastern edge of the Tengger Desert. Results Our results showed that the bacterial α and β diversity and network complexity in the biocrusts and subsoil increased with succession. In the process of succession, there were distinct differences observed in bacterial community diversity and network complexity and stability between biocrusts and subsoil. In particular, the subsoil bacterial network properties, including nodes, links, average links per node, average clustering coefficient, connectance and relative modularity, were significantly higher than those of biocrust in late succession. Based on piecewise SEM, we also found that succession, soil physicochemical conditions, and biocrust bacterial community composition were the strongest direct drivers of subsoil bacterial community composition. The plant communities and biocrust bacterial community composition directly drove the network complexity and stability of the subsoil bacterial community. Conclusion Our findings indicate that under the cover and protection of the biocrust layer, the diversity of the bacterial community in the subsoil layer increased more obviously, and the network was more complex and stable. This may emphasize the important roles of biocrusts as mediators of soil microbial communities. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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title_short |
Biocrust mediates the complexity and stability of bacterial networks in both biocrust and subsoil layers in the Tengger Desert |
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https://dx.doi.org/10.1007/s11104-023-06071-x |
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Ying, Zheng Haotian, Yang Xinrong, Li |
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score |
7.3999796 |