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Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline
Most land plants form mutualistic associations with arbuscular mycorrhizal fungi of the Glomeromycota, but recent studies have found that ancient plant lineages form mutualisms with Mucoromycotina fungi. Simultaneous associations with both fungal lineages have now been found in some plants, necessit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029179/ https://www.ncbi.nlm.nih.gov/pubmed/26613340 http://dx.doi.org/10.1038/ismej.2015.204 |
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author | Field, Katie J Rimington, William R Bidartondo, Martin I Allinson, Kate E Beerling, David J Cameron, Duncan D Duckett, Jeffrey G Leake, Jonathan R Pressel, Silvia |
author_facet | Field, Katie J Rimington, William R Bidartondo, Martin I Allinson, Kate E Beerling, David J Cameron, Duncan D Duckett, Jeffrey G Leake, Jonathan R Pressel, Silvia |
author_sort | Field, Katie J |
collection | PubMed |
description | Most land plants form mutualistic associations with arbuscular mycorrhizal fungi of the Glomeromycota, but recent studies have found that ancient plant lineages form mutualisms with Mucoromycotina fungi. Simultaneous associations with both fungal lineages have now been found in some plants, necessitating studies to understand the functional and evolutionary significance of these tripartite associations for the first time. We investigate the physiology and cytology of dual fungal symbioses in the early-diverging liverworts Allisonia and Neohodgsonia at modern and Palaeozoic-like elevated atmospheric CO(2) concentrations under which they are thought to have evolved. We found enhanced carbon cost to liverworts with simultaneous Mucoromycotina and Glomeromycota associations, greater nutrient gain compared with those symbiotic with only one fungal group in previous experiments and contrasting responses to atmospheric CO(2) among liverwort–fungal symbioses. In liverwort–Mucoromycotina symbioses, there is increased P-for-C and N-for-C exchange efficiency at 440 p.p.m. compared with 1500 p.p.m. CO(2.) In liverwort–Glomeromycota symbioses, P-for-C exchange is lower at ambient CO(2) compared with elevated CO(2). No characteristic cytologies of dual symbiosis were identified. We provide evidence of a distinct physiological niche for plant symbioses with Mucoromycotina fungi, giving novel insight into why dual symbioses with Mucoromycotina and Glomeromycota fungi persist to the present day. |
format | Online Article Text |
id | pubmed-5029179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50291792016-09-21 Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline Field, Katie J Rimington, William R Bidartondo, Martin I Allinson, Kate E Beerling, David J Cameron, Duncan D Duckett, Jeffrey G Leake, Jonathan R Pressel, Silvia ISME J Original Article Most land plants form mutualistic associations with arbuscular mycorrhizal fungi of the Glomeromycota, but recent studies have found that ancient plant lineages form mutualisms with Mucoromycotina fungi. Simultaneous associations with both fungal lineages have now been found in some plants, necessitating studies to understand the functional and evolutionary significance of these tripartite associations for the first time. We investigate the physiology and cytology of dual fungal symbioses in the early-diverging liverworts Allisonia and Neohodgsonia at modern and Palaeozoic-like elevated atmospheric CO(2) concentrations under which they are thought to have evolved. We found enhanced carbon cost to liverworts with simultaneous Mucoromycotina and Glomeromycota associations, greater nutrient gain compared with those symbiotic with only one fungal group in previous experiments and contrasting responses to atmospheric CO(2) among liverwort–fungal symbioses. In liverwort–Mucoromycotina symbioses, there is increased P-for-C and N-for-C exchange efficiency at 440 p.p.m. compared with 1500 p.p.m. CO(2.) In liverwort–Glomeromycota symbioses, P-for-C exchange is lower at ambient CO(2) compared with elevated CO(2). No characteristic cytologies of dual symbiosis were identified. We provide evidence of a distinct physiological niche for plant symbioses with Mucoromycotina fungi, giving novel insight into why dual symbioses with Mucoromycotina and Glomeromycota fungi persist to the present day. Nature Publishing Group 2016-06 2015-11-27 /pmc/articles/PMC5029179/ /pubmed/26613340 http://dx.doi.org/10.1038/ismej.2015.204 Text en Copyright © 2015 International Society for Microbial Ecology http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Field, Katie J Rimington, William R Bidartondo, Martin I Allinson, Kate E Beerling, David J Cameron, Duncan D Duckett, Jeffrey G Leake, Jonathan R Pressel, Silvia Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline |
title | Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline |
title_full | Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline |
title_fullStr | Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline |
title_full_unstemmed | Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline |
title_short | Functional analysis of liverworts in dual symbiosis with Glomeromycota and Mucoromycotina fungi under a simulated Palaeozoic CO(2) decline |
title_sort | functional analysis of liverworts in dual symbiosis with glomeromycota and mucoromycotina fungi under a simulated palaeozoic co(2) decline |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029179/ https://www.ncbi.nlm.nih.gov/pubmed/26613340 http://dx.doi.org/10.1038/ismej.2015.204 |
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