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      Little Cross-Feeding of the Mycorrhizal Networks Shared Between C 3- Panicum bisulcatum and C 4- Panicum maximum Under Different Temperature Regimes

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          Abstract

          Common mycorrhizal networks (CMNs) formed by arbuscular mycorrhizal fungi (AMF) interconnect plants of the same and/or different species, redistributing nutrients and draining carbon (C) from the different plant partners at different rates. Here, we conducted a plant co-existence (intercropping) experiment testing the role of AMF in resource sharing and exploitation by simplified plant communities composed of two congeneric grass species ( Panicum spp.) with different photosynthetic metabolism types (C 3 or C 4). The grasses had spatially separated rooting zones, conjoined through a root-free (but AMF-accessible) zone added with 15N-labeled plant (clover) residues. The plants were grown under two different temperature regimes: high temperature (36/32°C day/night) or ambient temperature (25/21°C day/night) applied over 49 days after an initial period of 26 days at ambient temperature. We made use of the distinct C-isotopic composition of the two plant species sharing the same CMN (composed of a synthetic AMF community of five fungal genera) to estimate if the CMN was or was not fed preferentially under the specific environmental conditions by one or the other plant species. Using the C-isotopic composition of AMF-specific fatty acid (C16:1ω5) in roots and in the potting substrate harboring the extraradical AMF hyphae, we found that the C 3- Panicum continued feeding the CMN at both temperatures with a significant and invariable share of C resources. This was surprising because the growth of the C 3 plants was more susceptible to high temperature than that of the C 4 plants and the C 3- Panicum alone suppressed abundance of the AMF (particularly Funneliformis sp.) in its roots due to the elevated temperature. Moreover, elevated temperature induced a shift in competition for nitrogen between the two plant species in favor of the C 4- Panicum, as demonstrated by significantly lower 15N yields of the C 3- Panicum but higher 15N yields of the C 4- Panicum at elevated as compared to ambient temperature. Although the development of CMN (particularly of the dominant Rhizophagus and Funneliformis spp.) was somewhat reduced under high temperature, plant P uptake benefits due to AMF inoculation remained well visible under both temperature regimes, though without imminent impact on plant biomass production that actually decreased due to inoculation with AMF.

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          Most cited references72

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          A meta-analysis of context-dependency in plant response to inoculation with mycorrhizal fungi.

          Ecology Letters (2010) 13: 394-407 Abstract Mycorrhizal fungi influence plant growth, local biodiversity and ecosystem function. Effects of the symbiosis on plants span the continuum from mutualism to parasitism. We sought to understand this variation in symbiotic function using meta-analysis with information theory-based model selection to assess the relative importance of factors in five categories: (1) identity of the host plant and its functional characteristics, (2) identity and type of mycorrhizal fungi (arbuscular mycorrhizal vs. ectomycorrhizal), (3) soil fertility, (4) biotic complexity of the soil and (5) experimental location (laboratory vs. field). Across most subsets of the data, host plant functional group and N-fertilization were surprisingly much more important in predicting plant responses to mycorrhizal inoculation ('plant response') than other factors. Non-N-fixing forbs and woody plants and C(4) grasses responded more positively to mycorrhizal inoculation than plants with N-fixing bacterial symbionts and C(3) grasses. In laboratory studies of the arbuscular mycorrhizal symbiosis, plant response was more positive when the soil community was more complex. Univariate analyses supported the hypothesis that plant response is most positive when plants are P-limited rather than N-limited. These results emphasize that mycorrhizal function depends on both abiotic and biotic context, and have implications for plant community theory and restoration ecology.
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            Roles of arbuscular mycorrhizas in plant phosphorus nutrition: interactions between pathways of phosphorus uptake in arbuscular mycorrhizal roots have important implications for understanding and manipulating plant phosphorus acquisition.

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              Rooting theories of plant community ecology in microbial interactions.

              Predominant frameworks for understanding plant ecology have an aboveground bias that neglects soil micro-organisms. This is inconsistent with recent work illustrating the importance of soil microbes in terrestrial ecology. Microbial effects have been incorporated into plant community dynamics using ideas of niche modification and plant-soil community feedbacks. Here, we expand and integrate qualitative conceptual models of plant niche and feedback to explore implications of microbial interactions for understanding plant community ecology. At the same time we review the empirical evidence for these processes. We also consider common mycorrhizal networks, and propose that these are best interpreted within the feedback framework. Finally, we apply our integrated model of niche and feedback to understanding plant coexistence, monodominance and invasion ecology. Copyright (c) 2010 Elsevier Ltd. All rights reserved.

                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                06 April 2018
                2018
                : 9
                : 449
                Affiliations
                [1]Laboratory of Fungal Biology, Ecology, Institute of Microbiology, Czech Academy of Sciences , Prague, Czechia
                Author notes

                Edited by: Ying Ma, University of Coimbra, Portugal

                Reviewed by: Raffaella Balestrini, Consiglio Nazionale delle Ricerche, Italy; Sergio Saia, Consiglio per la Ricerca in Agricoltura e l’Analisi dell’Economia Agraria, Italy

                *Correspondence: Jan Jansa, jansa@ 123456biomed.cas.cz

                This article was submitted to Plant Abiotic Stress, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2018.00449
                5897505
                d8dfd8e8-aa07-45a5-9eef-9ac2ed6c63b9
                Copyright © 2018 Řezáčová, Zemková, Beskid, Püschel, Konvalinková, Hujslová, Slavíková and Jansa.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 04 December 2017
                : 22 March 2018
                Page count
                Figures: 6, Tables: 0, Equations: 3, References: 90, Pages: 16, Words: 0
                Funding
                Funded by: Ministerstvo Školství, Mládeže a Telovýchovy 10.13039/501100001823
                Award ID: LK11224
                Funded by: Grantová Agentura Ceské Republiky 10.13039/501100001824
                Award ID: 18-04892S
                Funded by: Akademie Ved Ceské Republiky 10.13039/501100004240
                Award ID: RVO 61388971
                Categories
                Plant Science
                Original Research

                Plant science & Botany
                c3 and c4 photosynthesis,common mycorrhizal networks (cmns),temperature,natural 13c isotopic abundance,panicum sp.,arbuscular mycorrhiza,community,quantitative real-time pcr

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