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Phenotypic plasticity was detected in growth and leaf duration, the magnitude of which differed among populations with different seed source temperatures.
No significant difference was found in leaf duration, standing mean and MRT on the main stem between stands.
First, leaf duration (LDi, [i]d) in the period [0, T] is calculated: (5) LD i = ∫ 0 T [ f i (t ) – g i (t ) ] d t where fi(t) and gi(t) are the leaf production and loss at time t, respectively, both accumulated from the date of transplanting (t = 0) when no true leaf emerged.
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Foliar diseases appeared during the grain filling period and affected both, leaf area duration (LAD) and healthy area duration (HAD) during that period.
Are indicated: error (σE) and genotypic (σGE) variances, coefficient of variation (CV) and heritability (H) Analyses of variance on leaf length (Llength), leaf elongation duration (LED) and maximum leaf elongation rate (LERmax) considering two periods (spring and autumn) on 'Herbie'.
Analyses of variance on leaf length (Llength), leaf elongation duration (LED) and maximum leaf elongation rate (LERmax) for spring and autumn on 'Herbie' and for autumn on the core collection (Cc).
Data were collected on canopy temperature, relative growth rate, green flag leaf area duration, assimilates translocation and grain yield.
Spore fluxes were measured during two rain events and microclimate variables including air temperature, relative humidity and leaf wetness duration were recorded from the booting stage onwards.
Leaf wetness duration was in fact longer in the pure stand constituted of standard height resistant plants, which had the densest canopy.
Drought stress decreased leaf area duration, cumulative water transpired, net assimilation rate, mean transpiration rate, harvest index, and biomass yield in both varieties studied.
Protein concentration was related to protein weight and nitrogen nutrition index at flowering and to nitrogen uptake and leaf area duration after flowering.
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