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Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Modelling leaf phototropism in a cucumber canopy

Katrin Kahlen A B , Dirk Wiechers A and Hartmut Stützel A
+ Author Affiliations
- Author Affiliations

A Institute of Biological Production Systems, Leibniz Universität Hannover, Herrenhäuser Straße 2, 30419 Hannover, Germany.

B Corresponding author. Email: kahlen@gem.uni-hannover.de

This paper originates from a presentation at the 5th International Workshop on Functional–Structural Plant Models, Napier, New Zealand, November 2007.

Functional Plant Biology 35(10) 876-884 https://doi.org/10.1071/FP08034
Submitted: 22 February 2008  Accepted: 29 July 2008   Published: 11 November 2008

Abstract

Leaf phototropism might have significant effects on the light interception, dry matter production and yield of cucumber (Cucumis sativus L.). The objective of the present study was to model the phototropism of leaves in a greenhouse cucumber canopy. The dynamic structural model of cucumber using a parametric L-system was extended to mimic the leaf movement induced by gradients in the local light environment of each leaf. The red to far-red (R : FR) ratio is known to be a driving force in shade avoidance reactions of plants. In the model, R : FR ratios on the left and right leaf half of each individual leaf lamina were calculated and the change in tropism angle per phyllochron was based on the R : FR gradient across the leaf halves. The tropism angle of a leaf describes the deviation of the present leaf azimuth from the initial leaf orientation, which is predefined by the phyllotaxis of the plant. Even in its simple form, the model simulated photo-morphogenic canopy responses.

Additional keywords: Cucumis sativus L., functional–structural plant model, L-system, light, petiole bending, tropism.


Acknowledgements

We thank Michael Chelle and Pieter de Visser for the support of the CARIBU interface. This project has been supported in part by the German Research Foundation (DFG).


References


Allen MT, Prusinkiewicz P, Dejong TM (2005 ) Using L-systems for modeling source–sink interactions, architecture, and physiology of growing trees: the L-PEACH model. New Phytologist 166( ), 869–880.
Crossref | GoogleScholarGoogle Scholar | PubMed | [Verified 10 September 2008]

DeVisser PHB , Van der Heijden GWAM , Heuvelink E , Carvalho SMP (2007) Functional–structural modelling of crysanthemum. In ‘Functional–structural plant modelling in crop production.’ (Eds J Vos, LFM Marcelis, PHB deVisser, PC Struik, JB Evers) pp. 199–208. (Springer-Verlag: Dordrecht)

Dingkuhn M, Luquet D, Kim H, Tambour L, Clement-Vidal A (2006 ) EcoMeristem, a model of morphogenesis and competition among sinks in rice. 2. Simulating genotype responses to phosphorus deficiency. Functional Plant Biology 33( ), 325–337.
Crossref | GoogleScholarGoogle Scholar | [Verified 10 September 2008]

Farquhar GD, Von Caemmerer S, Berry JA (1980 ) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149( ), 78–90.
Crossref | GoogleScholarGoogle Scholar | [Verified 10 September 2008]

Franklin KA, Whitelam GC (2005 ) Phytochromes and shade-avoidance responses in plants. Annals of Botany 96( ), 169–175.
Crossref | GoogleScholarGoogle Scholar | PubMed | [Verified 10 September 2008]

Nguyen TMN (2006) Influence of water stress on leaf expansion and specific leaf area in cucumber (Cucumis sativus L.). MSc Thesis, Leibniz Universität, Hannover.

Prusinkiewicz P , Lindenmayer A (1990) ‘The algorithmic beauty of plants.’ (Springer-Verlag: New York)

Ruiz-Ramos M, Minguez MI (2005 ) ALAMEDA, a structural–functional model for faba bean crops: morphological parameterization and verification. Annals of Botany 97( ), 377–388.
Crossref | GoogleScholarGoogle Scholar | [Verified 10 September 2008]