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Paul C Struik

Publications and source records attributed to Paul C Struik.

9 recordsLinked to original sources

Cessation of tillering in spring wheat in relation to light interception and red : far-red ratio.

BACKGROUND AND AIMS: The production of axillary shoots (tillering) in spring wheat (Triticum aestivum) depends on intraspecific competition. The mechanisms that underlie this competition are complex, but light within the wheat canopy plays a key role. The main objectives of this paper are to analyse the effects of plant population density and shade on tillering dynamics of spring wheat, to assess the canopy conditions quantitatively at the time of tillering cessation, and to analyse the relationship between the tiller bud and the leaf on the same phytomer. METHODS: Spring wheat plants were grown at three plant population densities and under two light regimes (25 % and 100 % light). Tiller appearance, fraction of the light intercepted, and red : far-red ratio at soil level were recorded. On six sampling dates the growth status of axillary buds was analysed. KEY RESULTS: Tillering ceased earlier at high population densities and ceased earlier in the shade than in full sunlight. At cessation of tillering, both the fraction of light intercepted and the red : far-red ratio at soil level were similar in all treatments. Leaves on the same phytomer of buds that grew out showed more leaf mass per unit area than those on the same phytomer of buds that remained dormant. CONCLUSIONS: Tillering ceases at specific light conditions within the wheat canopy, independent of population density, and to a lesser extent independent of light intensity. It is suggested that cessation of tillering is induced when the fraction of PAR intercepted by the canopy exceeds a specific threshold (0.40-0.45) and red : far-red ratio drops below 0.35-0.40.

Photosynthesis↗

Mathematical review of literature to assess alternative electron transports and interphotosystem excitation partitioning of steady-state C3 photosynthesis under limiting light.

Linear whole-chain electron (e(-)) transport plays a dominant role in generating NADPH and ATP required for carbon fixation in chloroplasts. However, other e(-) pathways may be present to contribute to the flexibility of e(-) transport in meeting demands by various downstream metabolic processes. The estimation of the fluxes of these alternative pathways in vivo is difficult, as they are not amenable to direct experimental measurement. A recently developed model based on the generalized stoichiometry for the chloroplast e(-) transport pathways makes it possible to indirectly but quantitatively assess the fractions of e(-) that follow the alternative pathways. This model approach is used to review data from the literature on concurrent measurements of gas exchange and chlorophyll (Chl) fluorescence under steady-state, limiting light, non-photorespiratory conditions. The review suggests possible in vivo occurrence of cyclic e(-) transport (CET) under such conditions. About 10% of e(-) from the reduced ferredoxin follow the pseudocyclic mode, notably in support of nitrate reduction. The estimated fraction of e(-) from the reduced plastoquinone that follows the Q-cycle ( f(Q)) depends on the number of protons required per ATP synthesis. Our model approach also allows the excitation partitioning to photosystem II (PSII) to be assessed quantitatively. Most important, the model helps assess the limit value to uncertain physiological parameters and answer the 'what-if' question with regard to the effect of non-measured processes or measurement uncertainties on the estimations of alternative e(-) transports.

Electron Transport↗

Complex quality traits: now time to model.

A recently published dynamic peach model by Françoise Lescourret and Michel Génard simulates changes in quality during final stages of fruit growth. It predicts quality, emerging from complex processes and influenced by environment and management, remarkably well and describes complex emerging behaviour. The model could prove an excellent tool to integrate novel insight from metabolic profiling and pathways of taste-related compounds, ultimately enabling the analysis of gene networks responsible for fruit maturation processes.

Crops, Agricultural↗

QTL analysis and QTL-based prediction of flowering phenology in recombinant inbred lines of barley.

Combining ecophysiological modelling and genetic mapping has increasingly received attention from researchers who wish to predict complex plant or crop traits under diverse environmental conditions. The potential for using this combined approach to predict flowering time of individual genotypes in a recombinant inbred line (RIL) population of spring barley (Hordeum vulgare L.) was examined. An ecophysiological phenology model predicts preflowering duration as affected by temperature and photoperiod, based on the following four input traits: f(o) (the minimum number of days to flowering at the optimum temperature and photoperiod), theta1 and theta2 (the development stages for the start and the end of the photoperiod-sensitive phase, respectively), and delta (the photoperiod sensitivity). The model-input trait values were obtained from a photoperiod-controlled greenhouse experiment. Assuming additivity of QTL effects, a multiple QTL model was fitted for the model-input traits using composite interval mapping. Four to seven QTL were identified for each trait. Each trait had at least one QTL specific to that trait alone. Other QTL were shared by two or all traits. Values of the model-input traits predicted for the RILs from the QTL model were fed back into the ecophysiological model. This QTL-based ecophysiological model was subsequently used to predict preflowering duration (d) for eight field trial environments. The model accounted for 72% of the observed variation among 94 RILs and 94% of the variation among the two parents across the eight environments, when observations in different environments were pooled. However, due to the low percentage (34-41%) of phenotypic variation accounted for by the identified QTL for three model-input traits (theta1, theta2 and delta), the QTL-based model accounted for somewhat less variation among the RILs than the model using original phenotypic input trait values. Nevertheless, days to flowering as predicted from the QTL-based ecophysiological model were highly correlated with days to flowering as predicted from QTL-models per environment for days to flowering per se. The ecophysiological phenology model was thus capable of extrapolating (QTL) information from one environment to another.

Chromosome Mapping↗

Model analysis of flowering phenology in recombinant inbred lines of barley.

A generic model for flowering phenology as a function of daily temperature and photoperiod was applied to predict differences of flowering times among 96 individuals (including the two parents) of a recombinant inbred line population in barley (Hordeum vulgare L.). Because of the large number of individuals to study, there is a need for simple ways to derive model parameters for each genotype. Therefore the number of genotype-specific parameters was reduced to four, namely f(o) (the minimum number of days to flowering at the optimum temperature and photoperiod), (1) and (2) (the development stages for the start and the end of the photoperiod-sensitive phase, respectively), and delta (the photoperiod sensitivity). Values of these parameters were estimated using a newly described methodological framework based on data from a photoperiod-controlled experiment where plants were mutually transferred between long-day and short-day environments at regular intervals. This modelling approach was tested in eight independent field environments of different sowing dates in two growing seasons. The four-parameter model predicted 37-67% of observed phenotypic variation in an environment, 76% of variation in across-environment mean days to flowering among the genotypes, and 96% of variation in across-genotype mean among the eight environments. When all the observations of the 96 genotypes across the eight environments were pooled, the model explained 81% of the total variation. Sensitivity analysis showed that all four model parameters were important for predicting differences in flowering time among the genotypes; but their relative importance differed and the ranking was in the order of f(o), delta, theta1, and theta2. This study highlighted the potential of using ecophysiological models to assist the genetic analysis of quantitative crop traits whose phenotype is often environment-dependent.

Flowers↗

Towards a generic architectural model of tillering in Gramineae, as exemplified by spring wheat (Triticum aestivum).

This paper presents an architectural model of wheat (Triticum aestivum), designed to explain effects of light conditions at the individual leaf level on tillering kinetics. Various model variables, including blade length and curvature, were parameterized for spring wheat, and compared with winter wheat and other Gramineae species. The architectural model enables simulation of plant properties at the level of individual organs. Parameterization was based on data derived from an outdoor experiment with spring wheat cv. Minaret. Final organ dimensions of tillers could be modelled using the concept of relative phytomer numbers. Various variables in spring wheat showed marked similarities to winter wheat and other species, suggesting possibilities for a general Gramineae architectural model. Our descriptive model is suitable for our objective: investigating light effects on tiller behaviour. However, we plan to replace the descriptive modelling solutions by physiological, mechanistic solutions, starting with the localized production and partitioning of assimilates as affected by abiotic growth factors.

Models, Structural↗

In vivo uniform (15)N-isotope labelling of plants: using the greenhouse for structural proteomics.

Isotope labelling of proteins is important for progress in the field of structural proteomics. It enables the utilisation of the power of nuclear magnetic resonance spectroscopy (NMR) for the characterisation of the three-dimensional structures and corresponding dynamical features of proteins. The usual approach to obtain isotopically labelled protein molecules is by expressing the corresponding gene in bacterial or yeast host organisms, which grow on isotope-enriched media. This method has several drawbacks. Here, we demonstrate that it is possible to fully label a plant with (15)N-isotopes. The advantage of in vivo labelling of higher organisms is that all constituting proteins are labelled and become available as functional, post-translationally modified, correctly folded proteins. A hydroponics set-up was used to create the first example of a uniformly (15)N-labelled (> 98%) plant species, the potato plant (Solanum tuberosum L., cv. Elkana). Two plants were grown at low costs using potassium-[(15)N]-nitrate as the sole nitrogen source. At harvest time, a total of 3.6 kg of potato tubers and 1.6 kg of foliage, stolons and roots were collected, all of which were fully (15)N-labelled. Gram quantities of soluble (15)N-labelled proteins (composed mainly of the glycoprotein patatin and Kunitz-type protease inhibitors) were isolated from the tubers. NMR results on the complete proteome of potato sap and on an isolated protease inhibitor illustrate the success of the labelling procedure. The presented method of isotope labelling is easily modified to label other plants. Its envisioned impact in the field of structural proteomics of plants is discussed.

Carbon Isotopes↗