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Competitive interaction with keystone taxa induced negative priming under biochar amendments

BACKGROUND: Biochar amendments have been widely proposed as a conventional and efficient strategy to promote soil organic carbon (SOC) sequestration via negative priming. Unfortunately, the extent and biological mechanisms responsible for biochar-induced negative priming are still not fully understo...

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Autores principales: Chen, Lijun, Jiang, Yuji, Liang, Chao, Luo, Yu, Xu, Qinsong, Han, Cheng, Zhao, Qiguo, Sun, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526607/
https://www.ncbi.nlm.nih.gov/pubmed/31109381
http://dx.doi.org/10.1186/s40168-019-0693-7
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author Chen, Lijun
Jiang, Yuji
Liang, Chao
Luo, Yu
Xu, Qinsong
Han, Cheng
Zhao, Qiguo
Sun, Bo
author_facet Chen, Lijun
Jiang, Yuji
Liang, Chao
Luo, Yu
Xu, Qinsong
Han, Cheng
Zhao, Qiguo
Sun, Bo
author_sort Chen, Lijun
collection PubMed
description BACKGROUND: Biochar amendments have been widely proposed as a conventional and efficient strategy to promote soil organic carbon (SOC) sequestration via negative priming. Unfortunately, the extent and biological mechanisms responsible for biochar-induced negative priming are still not fully understood. Despite traditional explanations focused on the environmental filtering mechanisms of biochar amendments on microbial biomass and community composition underlying the priming effect on SOC dynamics, whether and how a biochar-induced competitive interaction with keystone taxa determines SOC mineralization in natural ecosystems has been minimally explored. RESULTS: Here, we paid particular attention to the relationships between the diversity and network structure of soil bacterial and fungal communities and SOC mineralization. A 3-year field experiment was conducted comprising five treatments: no fertilization, conventional fertilization, and conventional fertilization with three rates of biochar amendments. Biochar amendments considerably increased soil moisture capacity and pH and subsequently shaped the composition and co-occurrence networks of soil bacterial and fungal communities. Importantly, network analysis revealed that the biochar amendments triggered the competitive interaction with putative keystone taxa in the bacterial and fungal networks. Structural equation modeling suggested that the competitive interaction with keystone taxa promoted bacterial and fungal diversity and consequently reduced carbohydrate catabolism and soil metabolic quotient. Stable isotope probing incubations further provided consistent evidence of competition by keystone taxa with the increases in bacterial and fungal diversity under the biochar amendments. CONCLUSIONS: We found that biochar-induced competition with keystone taxa stimulated the bacterial and fungal diversity and consequently decreased SOC mineralization. The comprehensive understanding of the unexplored biological mechanisms underlying the biochar-induced negative priming may provide crucial implications for enabling SOC sequestration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0693-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-65266072019-05-28 Competitive interaction with keystone taxa induced negative priming under biochar amendments Chen, Lijun Jiang, Yuji Liang, Chao Luo, Yu Xu, Qinsong Han, Cheng Zhao, Qiguo Sun, Bo Microbiome Research BACKGROUND: Biochar amendments have been widely proposed as a conventional and efficient strategy to promote soil organic carbon (SOC) sequestration via negative priming. Unfortunately, the extent and biological mechanisms responsible for biochar-induced negative priming are still not fully understood. Despite traditional explanations focused on the environmental filtering mechanisms of biochar amendments on microbial biomass and community composition underlying the priming effect on SOC dynamics, whether and how a biochar-induced competitive interaction with keystone taxa determines SOC mineralization in natural ecosystems has been minimally explored. RESULTS: Here, we paid particular attention to the relationships between the diversity and network structure of soil bacterial and fungal communities and SOC mineralization. A 3-year field experiment was conducted comprising five treatments: no fertilization, conventional fertilization, and conventional fertilization with three rates of biochar amendments. Biochar amendments considerably increased soil moisture capacity and pH and subsequently shaped the composition and co-occurrence networks of soil bacterial and fungal communities. Importantly, network analysis revealed that the biochar amendments triggered the competitive interaction with putative keystone taxa in the bacterial and fungal networks. Structural equation modeling suggested that the competitive interaction with keystone taxa promoted bacterial and fungal diversity and consequently reduced carbohydrate catabolism and soil metabolic quotient. Stable isotope probing incubations further provided consistent evidence of competition by keystone taxa with the increases in bacterial and fungal diversity under the biochar amendments. CONCLUSIONS: We found that biochar-induced competition with keystone taxa stimulated the bacterial and fungal diversity and consequently decreased SOC mineralization. The comprehensive understanding of the unexplored biological mechanisms underlying the biochar-induced negative priming may provide crucial implications for enabling SOC sequestration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0693-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-20 /pmc/articles/PMC6526607/ /pubmed/31109381 http://dx.doi.org/10.1186/s40168-019-0693-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chen, Lijun
Jiang, Yuji
Liang, Chao
Luo, Yu
Xu, Qinsong
Han, Cheng
Zhao, Qiguo
Sun, Bo
Competitive interaction with keystone taxa induced negative priming under biochar amendments
title Competitive interaction with keystone taxa induced negative priming under biochar amendments
title_full Competitive interaction with keystone taxa induced negative priming under biochar amendments
title_fullStr Competitive interaction with keystone taxa induced negative priming under biochar amendments
title_full_unstemmed Competitive interaction with keystone taxa induced negative priming under biochar amendments
title_short Competitive interaction with keystone taxa induced negative priming under biochar amendments
title_sort competitive interaction with keystone taxa induced negative priming under biochar amendments
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526607/
https://www.ncbi.nlm.nih.gov/pubmed/31109381
http://dx.doi.org/10.1186/s40168-019-0693-7
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