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Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals
Trees and their associated rhizosphere organisms play a major role in mineral weathering driving calcium fluxes from the continents to the oceans that ultimately control long-term atmospheric CO(2) and climate through the geochemical carbon cycle. Photosynthate allocation to tree roots and their myc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510491/ https://www.ncbi.nlm.nih.gov/pubmed/26197714 http://dx.doi.org/10.1038/srep12187 |
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author | Schmalenberger, A. Duran, A. L. Bray, A. W. Bridge, J. Bonneville, S. Benning, L. G. Romero-Gonzalez, M. E. Leake, J. R. Banwart, S. A. |
author_facet | Schmalenberger, A. Duran, A. L. Bray, A. W. Bridge, J. Bonneville, S. Benning, L. G. Romero-Gonzalez, M. E. Leake, J. R. Banwart, S. A. |
author_sort | Schmalenberger, A. |
collection | PubMed |
description | Trees and their associated rhizosphere organisms play a major role in mineral weathering driving calcium fluxes from the continents to the oceans that ultimately control long-term atmospheric CO(2) and climate through the geochemical carbon cycle. Photosynthate allocation to tree roots and their mycorrhizal fungi is hypothesized to fuel the active secretion of protons and organic chelators that enhance calcium dissolution at fungal-mineral interfaces. This was tested using (14)CO(2) supplied to shoots of Pinus sylvestris ectomycorrhizal with the widespread fungus Paxillus involutus in monoxenic microcosms, revealing preferential allocation by the fungus of plant photoassimilate to weather grains of limestone and silicates each with a combined calcium and magnesium content of over 10 wt.%. Hyphae had acidic surfaces and linear accumulation of weathered calcium with secreted oxalate, increasing significantly in sequence: quartz, granite < basalt, olivine, limestone < gabbro. These findings confirmed the role of mineral-specific oxalate exudation in ectomycorrhizal weathering to dissolve calcium bearing minerals, thus contributing to the geochemical carbon cycle. |
format | Online Article Text |
id | pubmed-4510491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45104912015-07-28 Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals Schmalenberger, A. Duran, A. L. Bray, A. W. Bridge, J. Bonneville, S. Benning, L. G. Romero-Gonzalez, M. E. Leake, J. R. Banwart, S. A. Sci Rep Article Trees and their associated rhizosphere organisms play a major role in mineral weathering driving calcium fluxes from the continents to the oceans that ultimately control long-term atmospheric CO(2) and climate through the geochemical carbon cycle. Photosynthate allocation to tree roots and their mycorrhizal fungi is hypothesized to fuel the active secretion of protons and organic chelators that enhance calcium dissolution at fungal-mineral interfaces. This was tested using (14)CO(2) supplied to shoots of Pinus sylvestris ectomycorrhizal with the widespread fungus Paxillus involutus in monoxenic microcosms, revealing preferential allocation by the fungus of plant photoassimilate to weather grains of limestone and silicates each with a combined calcium and magnesium content of over 10 wt.%. Hyphae had acidic surfaces and linear accumulation of weathered calcium with secreted oxalate, increasing significantly in sequence: quartz, granite < basalt, olivine, limestone < gabbro. These findings confirmed the role of mineral-specific oxalate exudation in ectomycorrhizal weathering to dissolve calcium bearing minerals, thus contributing to the geochemical carbon cycle. Nature Publishing Group 2015-07-22 /pmc/articles/PMC4510491/ /pubmed/26197714 http://dx.doi.org/10.1038/srep12187 Text en Copyright © 2015, Macmillan Publishers Limited 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 | Article Schmalenberger, A. Duran, A. L. Bray, A. W. Bridge, J. Bonneville, S. Benning, L. G. Romero-Gonzalez, M. E. Leake, J. R. Banwart, S. A. Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals |
title | Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals |
title_full | Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals |
title_fullStr | Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals |
title_full_unstemmed | Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals |
title_short | Oxalate secretion by ectomycorrhizal Paxillus involutus is mineral-specific and controls calcium weathering from minerals |
title_sort | oxalate secretion by ectomycorrhizal paxillus involutus is mineral-specific and controls calcium weathering from minerals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510491/ https://www.ncbi.nlm.nih.gov/pubmed/26197714 http://dx.doi.org/10.1038/srep12187 |
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