Seed number, the most variable yield component of legumes is strongly affected by heat stress (HS) and water deficit (WD). The objective of this paper is to investigate whether HS and WD reduced seed number in field pea through their negative effects on biomass production rather than by specific effects on the developing reproductive organs. Several field and glasshouse experiments were carried out in southern France, in which HS and / or WD of various intensities, durations and positions in the plant lifecycle were imposed on several pea cultivars. WD and HS reduced seed number, in an intensity-dependent manner. They also changed the distribution of seeds along the stem. Plants subjected to WD and mild HS had more seeds on the basal phytomers than did control plants, making it possible to exclude direct effects of stress on seed development. In contrast, severe HS resulted in the immediate abortion of reproductive organs. WD and HS also decreased net photosynthesis (Pn), but only during the period of constraint. Quantitative relationships between Pn and soil water status and between Pn and leaf temperature were established. Nevertheless, in all cases there was a single linear relationship between final seed number and plant growth rate during the critical period for seed set (from the beginning of flowering to the beginning of seed fill for the last seed-bearing phytomer). This reflects the reproductive plasticity of pea, which adjusts the number of reproductive sinks in an apparent balance with assimilate availability in the plant.
. We thank Pascal Chapon for his dedicated technical help, the experimental station 'INRA LA Fage' as well as the 'Terrain d'experience' and 'PACE' platforms at CEFE (technical facilities of the Labex Centre Mediterranean de l'Environnement et de la Biodiversite, CEMEB) for providing all the facilities and technical support. F.F. was supported by a grant from1. Understanding the water-use of plants is timely under increasing drought stress due to climate change. Despite the crucial role of roots in water uptake, relationships between water-use and root traits are seldom considered. 2. Combining a functional trait-based approach with a water balance model, we tested whether root functional traits are related to spatial and temporal water-use among 12 Mediterranean rangeland species grown in common garden monocultures. Soil water content was monitored for 10 months, and the dynamics of water uptake of each species was modelled at a daily time step. Root functional traits were measured at two soil depths (shallow and deep soil). 3. Species with fast resource acquisition strategies in shallow soil, i.e. thin roots, maximised water uptake in a short period and consumed large amounts of water during periods of low water availability. Conversely, species with a more conservative root strategy, i.e. coarse roots, took up less water during the peak-growing season, maintained water uptake over a longer period of time and consumed less water during periods of low water availability. Deep root traits are strongly related to species' ability to take up water from deep soil. Deep roots with large diameters and low specific root length improve species' ability to reach water from deep soil. Biomass investment in the deep soil layer was positively related to the amount of water consumed during periods of low water availability. 4. Our results highlight that root functional traits influence a range of spatial and temporal water-use among Mediterranean rangeland species. They account for the amount of water taken up during dry periods but not during the entire growing season
Present work focussed on improving the description of organogenesis, morphogenesis and metabolism in a biophysical plant model (SUNFLO) applied to sunflower (Helianthus annuus L.). This first version of the model is designed for potential growth conditions without any abiotic or biotic stresses. Agreenhouse experiment was conducted to identify and estimate the phenotypic traits involved in plant productivity variability of 26 sunflower genotypes. The ability of SUNFLO to discriminate the genotypes was tested on previous results of a field survey aimed at evaluating the genetic progress since 1960. Plants were phenotyped in four directions; phenology, architecture, photosynthesis and biomass allocation. Twelve genotypic parameters were chosen to account for the phenotypic variability. SUNFLO was built to evaluate their respective contribution to the variability of yield potential. A large phenotypic variability was found for all genotypic parameters. SUNFLO was able to account for 80% of observed variability in yield potential and to analyse the phenotypic variability ofcomplex plant traits such as light interception efficiency or seed yield. It suggested that several ways are possible to reach high yields in sunflower. Unlike classical statistical analysis, this modelling approach highlights some efficient parametercombinations used by the most productive genotypes. The next steps will be to evaluate the genetic determinisms of thegenotypic parameters
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