Resource allocation to growth or luxury consumption drives mycorrhizal responses.
Identifieur interne : 000363 ( Main/Corpus ); précédent : 000362; suivant : 000364Resource allocation to growth or luxury consumption drives mycorrhizal responses.
Auteurs : Rohan C. Riley ; Timothy R. Cavagnaro ; Chris Brien ; F Andrew Smith ; Sally E. Smith ; Bettina Berger ; Trevor Garnett ; Rebecca Stonor ; Rhiannon K. Schilling ; Zhong-Hua Chen ; Jeff R. PowellSource :
- Ecology letters [ 1461-0248 ] ; 2019.
English descriptors
- KwdEn :
- MESH :
- chemical : Nitrogen, Phosphorus.
- Mycorrhizae, Resource Allocation, Symbiosis.
Abstract
Highly variable phenotypic responses in mycorrhizal plants challenge our functional understanding of plant-fungal mutualisms. Using non-invasive high-throughput phenotyping, we observed that arbuscular mycorrhizal (AM) fungi relieved phosphorus (P) limitation and enhanced growth of Brachypodium distachyon under P-limited conditions, while photosynthetic limitation under low nitrogen (N) was exacerbated by the fungus. However, these responses were strongly dependent on host genotype: only the faster growing genotype (Bd3-1) utilised P transferred from the fungus to achieve improved growth under P-limited conditions. Under low N, the slower growing genotype (Bd21) had a carbon and N surplus that was linked to a less negative growth response compared with the faster growing genotype. These responses were linked to the regulation of N : P stoichiometry, couples resource allocation to growth or luxury consumption in diverse plant lineages. Our results attest strongly to a mechanism in plants by which plant genotype-specific resource economics drive phenotypic outcomes during AM symbioses.
DOI: 10.1111/ele.13353
PubMed: 31370098
Links to Exploration step
pubmed:31370098Le document en format XML
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<term>Resource Allocation (MeSH)</term>
<term>Symbiosis (MeSH)</term>
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<term>Phosphorus</term>
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<front><div type="abstract" xml:lang="en">Highly variable phenotypic responses in mycorrhizal plants challenge our functional understanding of plant-fungal mutualisms. Using non-invasive high-throughput phenotyping, we observed that arbuscular mycorrhizal (AM) fungi relieved phosphorus (P) limitation and enhanced growth of Brachypodium distachyon under P-limited conditions, while photosynthetic limitation under low nitrogen (N) was exacerbated by the fungus. However, these responses were strongly dependent on host genotype: only the faster growing genotype (Bd3-1) utilised P transferred from the fungus to achieve improved growth under P-limited conditions. Under low N, the slower growing genotype (Bd21) had a carbon and N surplus that was linked to a less negative growth response compared with the faster growing genotype. These responses were linked to the regulation of N : P stoichiometry, couples resource allocation to growth or luxury consumption in diverse plant lineages. Our results attest strongly to a mechanism in plants by which plant genotype-specific resource economics drive phenotypic outcomes during AM symbioses.</div>
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<Abstract><AbstractText>Highly variable phenotypic responses in mycorrhizal plants challenge our functional understanding of plant-fungal mutualisms. Using non-invasive high-throughput phenotyping, we observed that arbuscular mycorrhizal (AM) fungi relieved phosphorus (P) limitation and enhanced growth of Brachypodium distachyon under P-limited conditions, while photosynthetic limitation under low nitrogen (N) was exacerbated by the fungus. However, these responses were strongly dependent on host genotype: only the faster growing genotype (Bd3-1) utilised P transferred from the fungus to achieve improved growth under P-limited conditions. Under low N, the slower growing genotype (Bd21) had a carbon and N surplus that was linked to a less negative growth response compared with the faster growing genotype. These responses were linked to the regulation of N : P stoichiometry, couples resource allocation to growth or luxury consumption in diverse plant lineages. Our results attest strongly to a mechanism in plants by which plant genotype-specific resource economics drive phenotypic outcomes during AM symbioses.</AbstractText>
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<Keyword MajorTopicYN="N">ecosystem function</Keyword>
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