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Genetic control of stomatal conductance in maize and conditional effects to water deficit and evaporative demand as revealed by phenomics
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International audience. Plants tend to decrease transpiration under water deficit and/or high evaporative demand by closing stomata. Stomatal conductance is central for the trades‐off between hydraulics and photosynthesis. We aimed at deciphering its genetic control and that of its responses to evaporative demand and water deficit, a nearly impossible task with gas exchanges measurements. Whole‐plant stomatal conductance was estimated via inversion of the Penman–Monteith equation from data of transpiration and plant architecture collected in a phenotyping platform. We have analyzed jointly 4 experiments with contrasting environmental conditions imposed to a panel of 254 maize hybrids. Estimated whole‐plant stomatal conductance closely correlated with gas‐exchange measurements and biomass accumulation rate. Sixteen robust quantitative trait loci (QTLs) were identified by genome wide association studies and co‐located with QTLs of transpiration and biomass. They accounted for 58% of the additive genetic variance and 40% of the genotype × environment interaction. Light, vapour pressure deficit (VPD), or soil water potential largely accounted for the differences in allelic effects between experiments, thereby providing strong hypotheses for mechanisms of stomatal control and explaining part of the observed genotype × environment interaction. Light positively affected the allelic effects of three QTLs (e.g. R2 = 0.74), whereas VPD and water deficit negatively affected the allelic effects of other four QTLs. The combination of SNP effects, as affected by environmental conditions, accounted for the variability of stomatal conductance across a range of hybrids and environmental conditions (R2 = 0.86). This approach may therefore contribute prediction of stomatal control in diverse environments and to breeding for water efficient maize.
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