19 research outputs found

    A multi-scale model of the interplay between cell signalling and hormone transport in specifying the root meristem of Arabidopsis thaliana

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    The growth of the root of Arabidopsis thaliana is sustained by the meristem, a region of cell proliferation and differentiation which is located in the root apex and generates cells which move shootwards, expanding rapidly to cause root growth. The balance between cell division and differentiation is maintained via a signalling network, primarily coordinated by the hormones auxin, cytokinin and gibberellin. Since these hormones interact at different levels of spatial organisation, we develop a multi-scale computational model which enables us to study the interplay between these signalling networks and cell cell communication during the specification of the root meristem. We investigate the responses of our model to hormonal perturbations, validating the results of our simulations against experimental data. Our simulations suggest that one or more additional components are needed to explain the observed expression patterns of a regulator of cytokinin signalling, ARR1, in roots not producing gibberellin. By searching for novel network components, we identify two mutant lines that affect significantly both root length and meristem size, one of which also differentially expresses a central component of the interaction network (SHY2). More generally, our study demonstrates how a multi-scale investigation can provide valuable insight into the spatio-temporal dynamics of signalling networks in biological tissues

    Finely-grained annotated datasets for image-based plant phenotyping

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    Image-based approaches to plant phenotyping are gaining momentum providing fertile ground for several interesting vision tasks where fine-grained categorization is necessary, such as leaf segmentation among a variety of cultivars, and cultivar (or mutant) identification. However, benchmark data focusing on typical imaging situations and vision tasks are still lacking, making it difficult to compare existing methodologies. This paper describes a collection of benchmark datasets of raw and annotated top-view color images of rosette plants. We briefly describe plant material, imaging setup and procedures for different experiments: one with various cultivars of Arabidopsis and one with tobacco undergoing different treatments. We proceed to define a set of computer vision and classification tasks and provide accompanying datasets and annotations based on our raw data. We describe the annotation process performed by experts and discuss appropriate evaluation criteria. We also offer exemplary use cases and results on some tasks obtained with parts of these data. We hope with the release of this rigorous dataset collection to invigorate the development of algorithms in the context of plant phenotyping but also provide new interesting datasets for the general computer vision community to experiment on. Data are publicly available at http://www.plant-phenotyping.org/datasets

    A method to determine the displacement velocity field in the apical region of the Arabidopsis root

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    In angiosperms, growth of the root apex is determined by the quiescent centre. All tissues of the root proper and the root cap are derived from initial cells that surround this zone. The diversity of cell lineages originated from these initials suggests an interesting variation of the displacement velocity within the root apex. However, little is known about this variation, especially in the most apical region including the root cap. This paper shows a method of determination of velocity field for this region taking the Arabidopsis root apex as example. Assuming the symplastic growth without a rotation around the root axis, the method combines mathematical modelling and two types of empirical data: the published velocity profile along the root axis above the quiescent centre, and dimensions of cell packet originated from the initials of epidermis and lateral root cap. The velocities, calculated for points of the axial section, vary in length and direction. Their length increases with distance from the quiescent centre, in the root cap at least twice slower than in the root proper, if points at similar distance from the quiescent centre are compared. The vector orientation depends on the position of a calculation point, the widest range of angular changes, reaching almost 90°, in the lateral root cap. It is demonstrated how the velocity field is related to both distribution of growth rates and growth-resulted deformation of the cell wall system. Also changes in the field due to cell pattern asymmetry and differences in slope of the velocity profile are modelled. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00425-012-1707-x) contains supplementary material, which is available to authorized users

    A cellular growth model for root tips

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    Growth of the root tip is modeled using a one-dimensional string of cells. Each cell is characterized by three distinct phases, division, elongation-only or maturity. In this model two hypothetical phytohormones, one produced at the root tip and the other at the shoot, determine the behavior of the cell, and therefore the growth of the entire tip. While the division rate is taken to be a step function of the string coordinate, the growth rate of each cell is assumed to be piecewise linear and composed of linear functions of cell length. Thereafter, suitable operators for the calculation of the velocity and relative growth rate distributions are given. The results of the model are finally compared to measurements of Arabidopsis thaliana, Nicotiana tabacum and Pisum sativum roots

    Photosynthesis in lightfleck areas of homobaric and heterobaric leaves

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    Leaves within a canopy are exposed to a spatially and temporally fluctuating light environment which may cause lateral gradients in leaf internal CO(2) concentration and diffusion between shaded and illuminated areas. In previous studies it was hypothesized that lateral CO(2) diffusion may support leaf photosynthesis, but the magnitude of this effect is still not well understood. In the present study homobaric leaves of Vicia faba or heterobaric leaves of Glycine max were illuminated with lightflecks of different sizes, mimicking sunflecks. Photosynthetic properties of the lightfleck areas were assessed with combined gas exchange measurements and chlorophyll fluorescence imaging. Lateral diffusion in homobaric leaves with an interconnected intercellular air space stimulated photosynthesis and the effect was largest in small lightfleck areas, in particular when plants were under drought stress. Such effects were not observed in the heterobaric leaves with strongly compartmented intercellular gas spaces. It is concluded that lateral diffusion may significantly contribute to photosynthesis of lightfleck areas of homobaric leaves depending on lightfleck size, lateral diffusivity, and stomatal conductance. Since homobaric leaf structures have been reported for many plant species, it is hypothesized that leaf homobary may have an impact on overall plant performance under conditions with a highly heterogeneous light environment

    Primary root growth: a biophysical model of auxin-related control

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    Plant hormones control many aspects of plant development and play an important role in root growth. Many plant reactions, such as gravitropism and hydrotropism, rely on growth as a driving motor and hormones as signals. Thus, modelling the effects of hormones on expanding root tips is an essential step in understanding plant roots. Here we achieve a connection between root growth and hormone distribution by extending a model of root tip growth, which describes the tip as a string of dividing and expanding cells. In contrast to a former model, a biophysical growth equation relates the cell wall extensibility, the osmotic potential and the yield threshold to the relative growth rate. This equation is used in combination with a refined hormone model including active auxin transport. The model assumes that the wall extensibility is determined by the concentration of a wall enzyme, whose production and degradation are assumed to be controlled by auxin and cytokinin. Investigation of the effects of auxin on the relative growth rate distribution thus becomes possible. Solving the equations numerically allows us to test the reaction of the model to changes in auxin production. Results are validated with measurements found in literature

    Spatio-temporal quantification of differential growth processes in root growth zones based on a novel combination of image sequence processing and refined concepts describing curvature production

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    Differential growth processes in root and shoot growth zones are governed by the transport kinetics of auxin and other plant hormones. While gene expression and protein localization of hormone transport facilitators are currently being unraveled using state-of-the-art techniques of live cell imaging, the quantitative analysis of growth reactions is lagging behind because of a lack of suitable methods. A noninvasive technique, based on digital image sequence processing, for visualizing and quantifying highly resolved spatio-temporal root growth processes was applied in the model plant Arabidopsis thaliana and was adapted to provide precise information on differential curvature production activity within the root growth zone. Comparison of root gravitropic curvature kinetics in wild-type and mutant plants altered in a facilitator for auxin translocation allowed the determination of differences in the location and in the temporal response of curvature along the growth zone between the investigated plant lines. The findings of the quantitative growth analysis performed here confirm the proposed action of the investigated transport facilitator. The procedure developed here for the investigation of differential growth processes is a valuable tool for characterizing the phenomenology of a wide range of shoot and root growth movements and hence facilitates elucidation of their molecular characterization
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