Plant Biol (Stuttg) 2003; 5(6): 642-650
DOI: 10.1055/s-2003-44691
Original Paper

Georg Thieme Verlag Stuttgart · New York

Expansion Kinematics are an Intrinsic Property of Leaf Development and are Scaled from Cell to Leaf Level at Different Nutrient Availabilities

A. Walter 1 , 2 , U. Roggatz 1 , 3 , U. Schurr 1 , 2
  • 1Botanical Institute, University of Heidelberg, Im Neuenheimer Feld 360, 69120 Heidelberg, Germany
  • 2Present address: Forschungszentrum Jülich, ICG III (Phytosphäre), Jülich, Germany
  • 3Present address: Botanical Institute, University of Heidelberg, Heidelberg, Germany
Further Information

Publication History

Publication Date:
02 February 2004 (online)

Abstract

Leaves of Nicotiana tabacum L. and Ricinus communis L. develop with a wide range of different final sizes due to leaf position and nutrient availability. The aim of this study was to investigate, on different organizational levels of leaf growth, which parameters are affected by external nutrient availability and which parameters are not affected and might thus be intrinsic, general patterns of growth that govern plant architecture. We found that leaf size and final cell size was larger with higher external nutrient availability, and that hexose concentrations in N. tabacum were lower with higher nutrient availability. Despite these differences, several dynamic parameters of leaf development were not affected by the nutrient treatment. Leaves of all sizes within a species exhibited the same relationship between relative leaf growth rate and relative leaf area (RLA), which is defined as the ratio of momentary and final leaf area. External nutrient availability did not affect chlorophyll concentration per parenchyma cell, which increased linearly with leaf development. Leaves of identical RLA exhibited identical cell density patterns within their interveinal tissue layers. This indicates a close connection between the kinematics of cell expansion and RLA and, hence, reveals that kinematics are an intrinsic property of growing leaves that can be scaled from the cell to the leaf level.

References

  • 1 Arnon D. I.. Copper enzymes in isolated chloroplasts. Polyphenol-oxidase in Beta vulgaris. .  Plant Physiology. (1949);  24 1-15
  • 2 Avery G. S.. Structure and development of tobacco leaves.  American Journal of Botany. (1933);  20 565-592
  • 3 Chapin F. S. III., Walter C. H. S., Clarkson D. T.. Growth response of barley and tomato to nitrogen stress and its control by abscisic acid, water relations and photosynthesis.  Planta. (1988);  173 352-366
  • 4 Erickson R. O., Michelini F. J.. The Plastochron Index.  American Journal of Botany. (1957);  44 297-305
  • 5 Fricke W., McDonald A. J. S., Mattson Djos L.. Why do leaves and leaf cells of N-limited barley elongate at reduced rates?.  Planta. (1997);  202 522-530
  • 6 Gastal F., Belanger G., Lemaire G.. A model of the leaf extension rate of tall fescue in response to nitrogen and temperature.  Annals of Botany. (1992);  70 437-442
  • 7 Granier C., Tardieu F.. Is thermal time adequate for expressing the effects of temperature on sunflower leaf development?.  Plant, Cell and Environment. (1998);  21 695-703
  • 8 Heckenberger U., Roggatz U., Schurr U.. Effect of drought stress on cytological status of Ricinus communis. .  Journal of Experimental Botany. (1998);  49 181-189
  • 9 Ingestad T.. Relative addition rate and external concentration; driving variables used in plant nutritional research.  Plant, Cell and Environment. (1982);  5 443-453
  • 10 Ingestad T., Ågren G. I.. Theories and methods on plant nutrition and growth.  Physiologia Plantarum. (1992);  84 177-184
  • 11 Ingestad T., Lund A. B.. Nitrogen stress in birch seedlings. I. Growth technique and growth.  Physiologia Plantarum. (1979);  45 137-148
  • 12 Jones M. G. K., Outlaw W. H., Lowry O. H.. Enzymatic assay of 10-7 to 10-14 moles of sucrose in plant tissues.  Plant Physiology. (1977);  60 379-383
  • 13 Lamoreaux R. J.. The Plastochron Index: A review after two decades of use.  American Journal of Botany. (1978);  65 586-593
  • 14 Maksymowych R.. Analysis of Leaf Development. Cambridge; Cambridge University Press (1973): 25
  • 15 Mitscherlich E. A.. Bodenkunde fuer Landwirte, Foerster und Gaertner, 7. ed. Berlin; Parey (1954): 47-49
  • 16 Natr L.. Influence of mineral nutrition on photosynthesis and the use of assimilates.  Photosynthesis and Productivity Differences Caused by the Environment. Proceedings of the IBP synthesis meeting 1973. (1975): 537-555
  • 17 Outlaw W. H., Fisher D. B.. Compartmentation in Vicia faba leaves I. Kinetics of 14C in the tissues following pulse labelling.  Plant Physiology. (1975);  55 699-703
  • 18 Pettigrew W. T., Vaughn K. C.. Physiological, structural, and immunological characterization of leaf and chloroplast development in cotton.  Protoplasma. (1998);  202 23-37
  • 19 Poethig R. S., Sussex I. M.. The developmental morphology and growth dynamics of tobacco leaf.  Planta. (1985 a);  165 158-169
  • 20 Poethig R. S., Sussex I. M.. The cellular parameters of leaf development in tobacco: a clonal analysis.  Planta. (1985 b);  165 170-184
  • 21 Radin J. W.. Control of plant growth by nitrogen: Differences between cereals and broadleaf species.  Plant, Cell and Environment. (1983);  6 65-68
  • 22 Radin J. W., Eidenbock M. P.. Hydraulic conductance as a factor limiting leaf expansion of phosphorous-deficient cotton plants.  Plant Physiology. (1984);  67 115-119
  • 23 Rao I. M., Fredeen A. L., Terry N.. Leaf phosphate status, photosynthesis, and carbon partitioning in sugar beet. III. Diurnal changes in carbon partitioning and carbon export.  Plant Physiology. (1990);  92 29-36
  • 24 Roggatz U., McDonald A. J. S., Stadenberg I., Schurr U.. Effect of nitrogen deprivation on cell division and expansion of Ricinus communis L.  Plant, Cell and Environment. (1999);  22 81-90
  • 25 Scheible W. R., Gonzales-Fontes A., Lauerer M., Müller-Röber B., Caboche M., Stitt M.. Nitrate acts as a signal to induce organic acid metabolism and repress starch metabolism in tobacco.  Plant Cell. (1997);  9 783-798
  • 26 Schmundt D., Stitt M., Jähne B., Schurr U.. Quantitative analysis of the local rates of growth of dicot leaves at a high temporal and spatial resolution, using image sequence analysis.  The Plant Journal. (1998);  16 505-514
  • 27 Schurr U.. Growth physiology: Approaches to a spatially and temporally varying problem. Behnke, H.-D., Lüttge, U., Esser, K., Kadereit, J. W., and Runge, M., eds. Progress in Botany, Vol. 59. Berlin; Springer Verlag (1997): 355-373
  • 28 Silk W. K., Erickson R. O.. Kinematics of plant growth.  Journal of Theoretical Biology. (1979);  76 481-501
  • 29 Snir N., Neumann P. M.. Mineral nutrient supply, cell wall adjustment and the control of leaf growth.  Plant, Cell and Environment. (1997);  20 239-246
  • 30 Terry N.. Developmental physiology of sugarbeet. II. Effect of temperature and nitrogen supply on the growth, soluble carbohydrate content and nitrogen content of leaves and roots.  Journal of Experimental Botany. (1970);  21 477-496
  • 31 Trapani N., Hall A. J.. Effects of leaf position and nitrogen supply on the expansion of leaves of field grown sunflower (Helianthus annuus L.).  Plant and Soil. (1996);  184 331-340
  • 32 Trapani N., Hall A. J., Weber M.. Effects of constant and variable nitrogen supply on sunflower (Helianthus annuus L.) leaf cell number and size.  Annals of Botany. (1999);  84 599-606
  • 33 Van Arendonk J. J. C. M., Niemann G. J., Boon J. J., Lambers H.. Effects of N-supply on anatomy and chemical composition of leaves of four grass species, belonging to the genus Poa, as determined by image-processing analysis and pyrolysis-mass spectrometry.  Plant Cell and Environment. (1997);  20 881-897
  • 34 Walter A., Schurr U.. The modular character of growth in Nicotiana tabacum plants under steady state nutrition.  Journal of Experimental Botany. (1999);  50 1169-1177
  • 35 Walter A., Schurr U.. Spatial variability of leaf development, growth and function. Marshall, B. and Roberts, J., eds. Leaf Development and Canopy Growth. Sheffield; Sheffield Academic Press (2000): 98-117

A. Walter

Forschungszentrum Jülich
ICG III (Phytosphäre)

52425 Jülich

Germany

Email: a.walter@fz-juelich.de

Section Editor: M. Riederer

    >