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E Costes

Publications and source records attributed to E Costes.

8 recordsLinked to original sources

Co-ordinated growth between aerial and root systems in young apple plants issued from in vitro culture.

BACKGROUND AND AIMS: In several species exhibiting a rhythmic aerial growth, the existence of an alternation between root and shoot growth has been demonstrated. The present study aims to investigate the respective involvement of the emergence of new organs and their elongation in relation to this phenomenon and its possible genotypic variation in young apple plants. METHODS: Two apple varieties, X6407 (recently named 'Ariane') and X3305 ('Chantecler' x 'Baujade'), were compared. Five plants per variety, issued from in vitro culture, were observed in minirhizotrons over 4 months. For each plant, root emergence and growth were observed twice per week. Growth rates were calculated for all roots with more than two segments and the branching density was calculated on primary roots. On the aerial part, the number of leaves, leaf area and total shoot length were observed weekly. KEY RESULTS: No significant difference was observed between varieties in any of the final characteristics of aerial growth. Increase in leaf area and shoot length exhibited a 3-week rhythm in X3305 while a weaker signal was observed in Ariane. The primary root growth rate was homogeneous between the plants and likewise between the varieties, while their branching density differed significantly. Secondary roots emerged rhythmically, with a 3-week and a 2-week rhythm, respectively, in X3305 and 'Ariane'. Despite a high intra-variety variability, significant differences were observed between varieties in the secondary root life span and mean length. A synchronism between leaf emergence and primary root growth was highlighted in both varieties, while an opposition phase was observed between leaf area increments and secondary root emergence in X3305 only. CONCLUSION: A biological model of dynamics that summarizes the interactions between processes and includes the assumption of a feedback effect of lateral root emergence on leaf emergence is proposed.

Cells, Cultured↗

Analysis of the plant architecture via tree-structured statistical models: the hidden Markov tree models.

Plant architecture is the result of repetitions that occur through growth and branching processes. During plant ontogeny, changes in the morphological characteristics of plant entities are interpreted as the indirect translation of different physiological states of the meristems. Thus connected entities can exhibit either similar or very contrasted characteristics. We propose a statistical model to reveal and characterize homogeneous zones and transitions between zones within tree-structured data: the hidden Markov tree (HMT) model. This model leads to a clustering of the entities into classes sharing the same 'hidden state'. The application of the HMT model to two plant sets (apple trees and bush willows), measured at annual shoot scale, highlights ordered states defined by different morphological characteristics. The model provides a synthetic overview of state locations, pointing out homogeneous zones or ruptures. It also illustrates where within branching structures, and when during plant ontogeny, morphological changes occur. However, the labelling exhibits some patterns that cannot be described by the model parameters. Some of these limitations are addressed by two alternative HMT families.

Combretaceae↗

Comparison methods for branching and axillary flowering sequences.

Comparing branching and axillary flowering patterns accurately is a major issue both in botany and in various agronomic contexts. Data take the form of sequences which naturally represent the underlying structural information of branching and axillary flowering patterns. Various comparison methods are proposed based either on sequence alignment or on the computation of dissimilarity measures between (hidden) Markovian models built from sets of sequences. Sequence alignment is a natural complement to the exploratory tools and statistical models proposed in Guédon et al. (J. Theor. Biol. 212 (2001) 481) with the distinctive feature of applying to individual sequences. Comparison methods may also be used to reveal some grouping within a set of sequences or to evaluate the strength of a predefined grouping of sequences. The proposed approach is illustrated by examples corresponding to different plant species and different biological or agronomic objectives.

Computer Simulation↗

Winter bud content according to position in 3-year-old branching systems of 'Granny Smith' apple.

An investigation was made of the number of preformed organs in winter buds of 3-year-old reiterated complexes of the 'Granny Smith' cultivar. Winter bud content was studied with respect to bud position: terminal buds were compared on both long shoots and spurs according to branching order and shoot age, while axillary buds were compared between three zones (distal, median and proximal) along 1-year-old annual shoots in order 1. The percentage of winter buds that differentiated into inflorescences was determined and the flowers in each bud were counted for each bud category. The other organ categories considered were scales and leaf primordia. The results confirmed that a certain number of organs must be initiated before floral differentiation occurred. The minimum limit was estimated at about 15 organs on average, including scales. Total number of lateral organs formed was shown to vary with both bud position and meristem age, increasing from newly formed meristems to 1- and 2-year-old meristems on different shoot types. These differences in bud organogenesis depending on bud position, were consistent with the morphogenetic gradients observed in apple tree architecture. Axillary buds did not contain more than 15 organs on average and this low organogenetic activity of the meristems was related to a low number of flowers per bud. In contrast, the other bud categories contained more than 15 differentiated organs on average and a trade-off was observed between leaf and flower primordia. The ratio between the number of leaf and flower primordia per bud varied with shoot type. When the terminal buds on long shoots and spurs were compared, those on long shoots showed more flowers and a higher ratio of leaf to flower primordia.

Cell Differentiation↗

Exploring within-tree architectural development of two apple tree cultivars over 6 years.

The present study addresses the prediction of apple tree development, taking into account both the number and within-tree position of tree components. The architectural development of two trees per scion cultivar, 'Fuji' and 'Braeburn', was studied by describing all shoots over 6 years. Flowering and fruiting were observed over 3 years. The description included different scales [entire trees, axes, growth units (GUs) and metamers], and the analysis compared all axes of the trees as a function of their branching order and age. Three main aspects of vegetative development were investigated: the quantity of primary growth; the number and nature of developing axillary shoots; and meristem death. Results confirm the existence of within-tree morphological gradients, and show that the decrease in growth was comparable in magnitude for all axes and GUs, irrespective of their position. This decrease results from a reduction in the number of metamers per GU, which was modelled by an exponential function. The decrease in growth involved changes in the number and nature of the axillary shoots, which could be described by simple functions. The probability of spur death was constant over the years but differed according to cultivar and type of bearing shoot. The within-tree probability of flowering and fruiting was predictable for 'Braeburn' because axes, regardless of their position and type, had a high probability of flowering and a low probability of fruit set which led to a regular bearing habit. In contrast, 'Fuji' had an alternating bearing behaviour that was more complex to predict. This appeared to result from a synchronized increase in the probability that all GUs at tree scale are floral, combined with a high probability of fruit set. The consequences of these results for both yield prediction and architectural simulations are discussed.

Flowers↗

Application of architectural analysis and AMAPmod methodology to study dwarfing phenomenon: the branch structure of 'Royal Gala' apple grafted on dwarfing and non-dwarfing rootstock/interstock combinations.

Architectural analysis was applied to study branch development of 'Royal Gala' apple trees grafted with dwarfing and non-dwarfing rootstock/interstock combinations, which had been chosen to produce trees with a wide range of vigour. Using AMAPmod methodology, the structure of 3-year-old branches was described at four levels of representation: branch; annual shoot; growth unit; and node. Three types of growth units were distinguished: extension growth unit (vegetative unit with internode extension); vegetative spur with minimal internode extension; and fruiting spur or bourse. The aim of the analysis was to describe exactly how the rootstock/interstock combinations affected the structure building process. The number of extension growth units, vegetative spurs and fruiting spurs per annual shoot changed over the years, but this was not affected by rootstock/interstock combination. Compared with MM.106 rootstock, M.9 rootstock reduced the number of nodes per extension growth unit. In most cases, rootstock/interstock combination had no effect on the linear relationship between extension growth unit length and node number (R(2) = 0.88). Average internode length depended on unit node number, with internodes being shorter for units with fewer nodes. Thus the difference in apple branch size induced by the rootstock/interstock combinations was mainly due to a reduction in the length and number of neoformed nodes produced on extension growth units. As percentage budbreak of axillary buds on extension growth units was not affected by rootstock/interstock combination, differences in numbers of axillary annual shoots per branch were entirely due to differences in the total numbers of nodes extended during the previous year.

Algorithms↗

Modelling branching patterns on 1-year-old trunks of six apple cultivars.

The structure resulting from branching on 1-year-old apple tree trunks was analysed in a set of apple cultivars with diverse branching and fruiting habits. Four different lateral types borne on successive nodes were observed when vegetative and flowering fates, as well as sylleptic and proleptic branching, were taken into account. The location and grouping of lateral types along the trunk were analysed for all cultivars, but are detailed for one cultivar only. This cultivar showed a succession of zones, each zone being characterized by its composition of lateral types. Statistical models-hidden semi-Markov chains-were built to take this structure into account and to characterize the cultivar's specific branching pattern. The models showed that most of the branching zones had a similar location in the different cultivars, even though zone composition and zone length differed among cultivars. On a more detailed scale, the nodes bearing a lateral, regardless of its type, were frequently followed by latent buds. The validity of the models and their biological interpretation are discussed with respect to parent shoot dynamics, hormonal gradients and competition between neighbouring buds.

Malus↗

Pattern analysis in branching and axillary flowering sequences.

In the architectural approach to the study of plants, a major issue is to analyse branching and axillary flowering patterns. Due to the structured expression of the branching process and the noisy character of the observed patterns, we propose an analysis framework which is both structural and probabilistic. Data take the form of sequences which naturally represent the underlying structural information of branching and axillary flowering patterns and allow the application of a large number of methods ranging from exploratory analysis to stochastic modeling. The primary aim of the proposed analysis methods is to reveal patterns not directly apparent in the data, and thus to deepen our biological understanding of the underlying mechanisms that control the branching and the axillary flowering of plants over time and space. The proposed approach is illustrated using a set of examples corresponding to different plant species and different biological or agronomic objectives.

Models, Biological↗