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

Integrated responses of rosette organogenesis, morphogenesis and architecture to reduced incident light in Arabidopsis thaliana results in higher efficiency of light interception

Karine Chenu A , Nicolas Franck A , Jean Dauzat B , Jean-François Barczi B , Hervé Rey B and Jérémie Lecoeur A C
+ Author Affiliations
- Author Affiliations

A Institut National de la Recherche Agronomique (INRA) — Ecole Nationale Supérieure d’Agronomie (ENSA), Laboratoire d’Ecophysiologie des Plantes sous Stress Environnementaux (LEPSE) UMR 759, 2 Place Viala, 34060 Montpellier, France.

B Centre de Coopération International en Recherche Agronomique pour le développement (CIRAD), UMR Botanique et Bioinformatique de l’Architecture des Plantes (AMAP), Bvd de la Lironde, 34398 Montpellier, France.

C Corresponding author. Email: lecoeur@ensam.inra.fr

Functional Plant Biology 32(12) 1123-1134 https://doi.org/10.1071/FP05091
Submitted: 15 April 2005  Accepted: 16 August 2005   Published: 1 December 2005

Abstract

Plants have a high phenotypic plasticity in response to light. We investigated changes in plant architecture in response to decreased incident light levels in Arabidopsis thaliana (L.) Heynh, focusing on organogenesis and morphogenesis, and on consequences for the efficiency of light interception of the rosette. A. thaliana ecotype Columbia plants were grown under various levels of incident photosynthetically active radiation (PAR), with blue light (BL) intensity proportional to incident PAR intensity and with a high and stable red to far-red light ratio. We estimated the PAR absorbed by the plant, using data from precise characterisation of the light environment and 3-dimensional simulations of virtual plants generated with AMAPsim software. Decreases in incident PAR modified rosette architecture; leaf area decreased, leaf blades tended to be more circular and petioles were longer and thinner. However, the efficiency of light interception by the rosette was slightly higher in plants subjected to lower PAR intensities, despite the reduction in leaf area. Decreased incident PAR delayed leaf initiation and slowed down relative leaf expansion rate, but increased the duration of leaf expansion. The leaf initiation rate and the relative expansion rate during the first third of leaf development were related to the amount of PAR absorbed. The duration of leaf expansion was related to PAR intensity. The relationships identified could be used to analyse the phenotypic plasticity of various genotypes of Arabidopsis. Overall, decreases in incident PAR result in an increase in the efficiency of light interception.

Keywords: absorbed radiation, Arabidopsis thaliana, blue light, leaf development, leaf expansion, light intensity, phenotypic plasticity, rosette architecture.


Acknowledgments

We thank A. Christophe for advice concerning light quality and S. Lagier for technical assistance. This research was partly supported by a grant from the European Research Training Network (HPRN-CT-2002–00267).


References


Barczi, JF , de Reffye, P ,  and  Caraglio, Y (1997). Essai sur l’identification et la mise en œuvre des paramètres nécessaires à la simulation d’une architecture végétale. In ‘Modélisation et simulation de l’architecture des végétaux’. pp. 205–254. (INRA Editions: Paris)

Ballaré CL (1999) Keeping up with the neighbours: phytochrome sensing and other signalling mechanisms. Trends in Plant Science 4, 97–102.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Bertero H (2001) Effects of photoperiod, temperature and radiation on the rate of leaf appearance in quinoa (Chenopodium quinoa Willd.) under field conditions. Annals of Botany 87, 495–502.
Crossref | GoogleScholarGoogle Scholar | open url image1

Dauzat J, Eroy MN (1997) Simulating light regime and intercrop yields in coconut based farming systems. European Journal of Agronomy 7, 63–74.
Crossref | GoogleScholarGoogle Scholar | open url image1

Eskins K (1992) Light-quality effects on Arabidopsis development. Red, blue and far-red regulation of flowering and morphology. Physiologia Plantarum 86, 439–444.
Crossref | GoogleScholarGoogle Scholar | open url image1

Fahn, A (1990). ‘Plant anatomy.’ (Pergamon Press: Oxford)

Freixes S, Thibaud MC, Tardieu F, Muller B (2002) Root elongation and branching is related to local hexose concentration in Arabidopsis thaliana seedlings. Plant, Cell & Environment 25, 1357–1366.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gautier H, Varlet-Grancher C (1996) Regulation of leaf growth of grass by blue light. Physiologia Plantarum 98, 424–430.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gautier H, Mech R, Prusinkiewicz P, Varlet-Grancher C (2000) 3D Architectural modelling of aerial photomorphogenesis in white clover (Trifolium repens L.) using L-systems. Annals of Botany 85, 359–370.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gautier H, Varlet-Grancher C, Membre JM (2001) Plasticity of petioles of white clover (Trifolium repens) to blue light. Physiologia Plantarum 112, 293–300.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Gianoli E (2001) Lack of differential plasticity to shading of internodes and petioles with growth habit in Convolvulus arvensis (Convolvulaceae). International Journal of Plant Sciences 162, 1247–1252.
Crossref | GoogleScholarGoogle Scholar | open url image1

Granier C, Tardieu F (1998) Is thermal time adequate for expressing the effects of temperature on sunflower leaf development? Plant, Cell & Environment 21, 695–703.
Crossref | GoogleScholarGoogle Scholar | open url image1

Granier C, Tardieu F (1999) Leaf expansion and cell division are affected by reducing absorbed light before but not after the decline in cell division rate in the sunflower leaf. Plant, Cell & Environment 22, 1365–1376.
Crossref | GoogleScholarGoogle Scholar | open url image1

Granier C, Massonnet C, Turc O, Muller B, Chenu K, Tardieu F (2002) Individual leaf development in Arabidopsis thaliana: a stable thermal-time-based programme. Annals of Botany 89, 595–604.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Grime JP, Jeffrey W (1965) Seedling establishment in vertical gradients of sunlight. Journal of Ecology 53, 621–642. open url image1

Hussey G (1963) Growth and development in the young tomato II. The effect of defoliation on the development of the shoot apex. Journal of Experimental Botany 14, 326–333. open url image1

Kemp DR (1981) The growth rate of wheat leaves in relation to the extension zone sugar concentration manipulated by shading. Journal of Experimental Botany 32, 141–150. open url image1

Kozuka T, Horiguchi G, Kim G-T, Ohgishi M, Sakai T, Tsukaya H (2005) The different growth reponses of the Arabidopsis thaliana leaf blade and the petiole during shade avoidance are regulated by photoreceptors and sugar. Plant & Cell Physiology 46, 213–223.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Lecoeur J, Ney B (2003) Change with time in potential radiation-use efficiency in field pea. European Journal of Agronomy 19, 91–105.
Crossref | GoogleScholarGoogle Scholar | open url image1

Milthorpe FL, Newton P (1963) Studies on the expansion of the leaf surface. III. The influence of radiation on cell division and leaf expansion. Journal of Experimental Botany 14, 483–495. open url image1

Ney B, Turc O (1993) Heat-unit-based description of the reproductive development of pea. Crop Science 33, 510–514. open url image1

Pearcy RW, Yang W (1998) The functional morphology of light capture and carbon gain in the Redwood forest understorey plant Adenocaulon bicolor Hook. Functional Ecology 12, 543–552.
Crossref | GoogleScholarGoogle Scholar | open url image1

Pieters GA (1985) Effects of irradiation level on leaf growth of sunflower. Physiologia Plantarum 65, 263–268. open url image1

Rawson HM, Dunstone RL (1986) Simple relationships describing the responses of leaf growth to temperature and radiation in sunflower. Australian Journal of Plant Physiology 13, 321–327. open url image1

Sager JC, Smith WO, Edwards JL, Cyr KL (1988) Photosynthetic efficiency and phytochrome photoequilibria determination using spectral data. American Society of Agricultural Engineers 31, 1882–1889. open url image1

Smith H (1982) Light quality, photoperception, and plant strategy. Annual Review of Plant Physiology 33, 481–518.
Crossref | GoogleScholarGoogle Scholar | open url image1

Stuefer JF, Huber H (1998) Differential effects of light quantity and spectral light quality on growth, morphology and development of two stoniferous Potentilla species. Oecologia 117, 1–8.
Crossref | GoogleScholarGoogle Scholar | open url image1

Sullivan JA, Deng XW (2003) From seed to seed: the role of photoreceptors in Arabidopsis development. Developmental Biology 260, 289–297.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Sultan SE (2000) Phenotypic plasticity for plant development, function and life history. Trends in Plant Science 5, 537–542.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Tardieu F (2003) Virtual plants: modelling as a tool for the genomics of tolerance to water deficit. Trends in Plant Science 8, 9–14.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Tsukaya H, Kozuka T, Gyung Tae K (2002) Genetic control of petiole length in Arabidopsis thaliana. Plant & Cell Physiology 43, 1221–1228.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Wheeler RM, Mackowiak CL, Sager JC (1991) Soybean stem growth under high-pressure sodium with supplemental blue lighting. Agronomy Journal 83, 903–906.
PubMed |
open url image1