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Modelling floral induction for different apple tree cultivars: an innovative approach to disentangle the intertwined effects of hormonal signals, carbohydrate
status and plant architecture Benoit Pallas
To cite this version:
Benoit Pallas. Modelling floral induction for different apple tree cultivars: an innovative approach to disentangle the intertwined effects of hormonal signals, carbohydrate status and plant architecture. AgreenSkills Annual Meeting, Oct 2014, Toulouse, France. 2014. �hal-02794925�
Modelling floral induction for different apple tree cultivars: an innovative approach to disentangle
the intertwined effects of hormonal signals, carbohydrate status and plant architecture
Benoît Pallas
(Outgoing Fellow, INRA, UMR AGAP)
Host institution : University of QueensLand
Supervisor : Jim Hanan
Dates of mobility : February 2015 – March 2016
Context and state of art
• Alternate bearing is of key importance for apple tree production and is
characterised by a low production in
OFF years and a high production of too
many fruits of poor quality in ON years.
• The use of chemical products reducing
fruit set during ON years is going to be gradually forbidden.
• Growers are looking for alternative solutions to reduce alternate bearing.
• Preliminary analyses on a bi-parental population showed a large genetic variability in
tree production pattern (irregular, biennial,
regular bearing) (Durand et al., 2012)
• QTLs related to these production and flowering
patterns were indentified (Guitton et al., 2012)
A
B
A
B
Main hypothesis and scientific questions
•
The variability in production patterns is mainly related to the variability in floralinduction occuring one year before flowering in apical and lateral meristems.
• Physiological determinants of floral induction variability are still largely unknown.
• 2 Hypotheses are proposed based on experimental results :
- trophic competition for carbohydrate between growing fruits and meristems
could decrease floral induction during ‘ON’ years (Nielsen and Denis, 2000)
- gibberelins produced by fruit seeds could also lead to a decrease in floral
induction (Bangerth. 2009)
… but production patterns are also strongly correlated with plant architecture (Lauri
and Trottier, 2004) (e.g. genotypes with long shoots display more regular bearing patterns)
• The respective effects of hormones, carbohydrate balance and architecture are difficult to disentagle using experimental approaches.
Using a
modelling approach
to better analyze the
interactions
between these different aspects of plant development and
functionning.
Objectives and description of the project
• The main objective is to include in the Functional Structural Plant Model MAppleT
(Costes et al. 2008) simulating plant architecture over years a sub model to simulate hormonal and carbohydrate fluxes between leaves, fruits and meristems.
•
This sub model will be developped inUniversity of QueensLand.
• A first model based on models developped at UQ (C-TRAM for carbohydrate fluxes (Cieslak et al., 2011); models for translocation of hormones (Renton et al., 2013)) will be implemented for the sub-unit composed of a
bourse and a bourse shoot in which floral
induction occurs.
•
The model will be built in L-Systems with the plant modelling environment L-Studio(Karwowski and Prunsinkiewicz, 2004) and will then be integrated in MAppleT to capture the variability in floral induction within plant structure and analyze the impact of plant architecture.
• The model will be calibrated and validated with experiments carried out in Montpellier
First activities and results
• A first experiment was carried out in
summer 2014 in Montpellier on a segregating population (X3263 x Belrène)
• The objectives of the experiment were to :
- define a sub-population displaying large
variability in production patterns. (biennial, irregular, regular) based on floral sequence analysis (Fig. 7).
- quantify hormonal contents in organs
and plant trophic status (photosynthesis
activity (Fig.8), non structural hormonals
contents) for the genotypes with
contrasting production patterns.
• A first dataset useful for modelling
activities is available. This dataset will be complemented in 2015.
References
Bangerth. 2009. Sci. Hort. 122: 153-163; Cieslak et al. 2011. Ann. Bot. 107: 747-764; Costes et al. 2008. Funct. Plant Biol. 35: 936-950; Guitton et al. 2012. J Exp Bot. 63: 131-149; Durand et al. 2013. J Exp Bot 64: 5099-5113. Karwowski and Prusinkiewicz. 2004. FSPM Proceedings. 403-405; Lauri and Trottier. 2004. New Phytol. 163: 533-546; Nielsen and Denis. 2000. Act. Hort. 527: 137-146; Renton et al. 2012. New Phytol. 194: 704-715.
Fig 1. Trees in ON and OFF years (A, B, respectively)
Fig 2. QTLs detected for BBI (index of
alternance) on chromosom 4, for a segregating population (Starkinson x Granny) (Guitton et al., 2012)
Fig 3. Example of two contrasted production
patterns (number of fruits) of two genotypes of a segregating population (Belrène x X3263)
Fig 4. Output of MappleT (Costes et al. ,2008)
Fig 5. The L-Studio modelling environment
(algorithmicbotany.org/lstudio/whatis.html)
Fig 6. A bourse/ shoot
bourse structure.
M: apical meristem (in which floral induction occurs); BS : bourse shoot; LS : bourse shoot leaf; B : bourse; LB: leaf bourse ;F: fruit F B BS LS M LB
Fig 8. Leaf net assimilation for the genotypes with different
production patterns (BvsB & Desynch : regular genotypes, ON & OFF: biennial genotypes in ON or OFF years)
Production type
BvsB Desync V Desyn F ON OFF
Ne t as s imi lation ( molC0 2 m -2 s -1 ) 0 2 4 6 8 10 12 14 b b b a b Type effect **
Fig 7. PCA analysis on production variables on the
genotypes of the X3263xBelrène population. (bi-prod, biennial genotypes, in ON or OFF years. Reg: regular genotypes. Prod – and Prod + refer to genotypes with low or high production).