ArticleAnnals of botany2018
Seeking stable traits to characterize the root system architecture. Study on 60 species located at two sites in natura.
Article in Annals of botany, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- A starting guide to root ecology: strengthening ecological concepts and standardising root classification, sampling, processing and trait measurements.The New phytologist · 2021Review
- Genetic Variation in Root Architectural Traits inFrontiers in plant science · 2021Article
- Genotypic diversity and plasticity of root system architecture to nitrogen availability in oilseed rape.PloS one · 2021Article
- Modelling time variations of root diameter and elongation rate as related to assimilate supply and demand.Journal of experimental botany · 2020Article
- Analysis and Modeling of the Variations of Root Branching Density Within Individual Plants and Among Species.Frontiers in plant science · 2019Article
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Authors and funding
2 authors.
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Abstract
Background and Aims: In several disciplines, identifying relevant root traits to characterize the root system architecture of species or genotypes is a crucial step. To address this question, we analysed the inter-specific variations of root architectural traits in two contrasting environments. Methods: We sampled 60 species in natura, at two sites, each presenting homogeneous soil conditions. We estimated for each species and site a set of five traits used for the modelling of the root system architecture: extreme tip diameters (Dmin and Dmax), relative diameter range (Drange), mean inter-branch distance (IBD) and dominance slope between the diameters of parent and lateral roots (DlDm). Key Results: The five traits presented a highly significant species effect, explaining between 77 and 98 % of the total variation. Dmin, Dmax and Drange were particularly determined by the species, while DlDm and IBD exhibited a higher percentage of environmental variations. These traits make it possible to confirm two main axes of variation: 'fineness-density' (defined by Dmin and IBD) and 'dominance-heterorhizy' (DlDm and Drange), that together accounted for 84 % of the variations observed. Conclusions: We confirmed the interest of these traits in the characterization of the root system architecture in ecology and genetics, and suggest using them to enrich the 'root economic spectrum'.
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