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Oecologia

, Volume 104, Issue 1, pp 17–23 | Cite as

Growth, photosynthesis and storage of carbohydrates and nitrogen in Phaseolus lunatus in relation to resource availability

  • H. A. Mooney
  • K. Fichtner
  • E.-D. Schulze
Original Paper

Abstract

Growth, photosynthesis, and storage of nitrogen (N) and total non-structural carbohydrates (TNC) of a perennial wild type and an annual cultivar of lima bean (Phaseolus lunatus) were examined at different light intensities and N supplies. Relative growth rate and photosynthesis increased with light and N availability. N limitation enhanced biomass allocation into root rather than into shoot, while light limitation enhanced growth of leaf area. The TNC concentrations increased with light intensity and thus with photosynthesis, while the concentrations of organic N and nitrate decreased. Increasing N supply had the opposite effect. Therefore, TNC and organic N concentrations were negatively correlated (r=−0.90). Pool size of N or TNC increased with N and light availability when either resource was non-limiting, but increased little or remained constant when either resource was limiting. Storage reached a minimum when both resources were supplied at an equal rate.

Key words

Carbohydrate Growth Nitrogen Phaseolus lunatus Storage 

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References

  1. Beevers L, Hageman RH (1980) Nitrate and nitrite reduction. In: Miflin BJ (ed) The biochemistry of plants, vol 5. Academic Press, London, pp 115–118Google Scholar
  2. Björkman O (1981) Responses to different quantum flux densities. In: Lange OL, Nobel OS, Osmond CB, Ziegler H (eds) Encyclopedia of plant physiology, vol 12A. Springer, Berlin Heidelberg New York, pp 57–107Google Scholar
  3. Brouwer R (1962) Nutritive influences on the distribution of dry matter in the plant. Neth J Agric Sci 10:399–392Google Scholar
  4. Chapin FS, Schulze E-D, Mooney HA (1990) The ecology and economics of storage in plants. Annu Rev Ecol Syst 21:423–447Google Scholar
  5. Clarkson DT (1985) Factors affecting mineral acquisition by plants. Annu Rev Ecol Syst 21:423–447Google Scholar
  6. Fichtner K, Schulze E-D (1992) The effect of nitrogen nutrition on growth and biomass partitioning in annual plant originating from habitats of different nitrogen availability. Oecologia 92: 236–241Google Scholar
  7. Fichtner K, Quick WP, Schulze E-D, Mooney HA, Rodermel SR, Bogorad L, Stitt M (1993) Decreased ribulose-1,5-bisphosphate carboxilase-oxygenase in transgenic tobacco transformed with “antisense” rbcS. V. Relationship between photosynthetic rate, storage strategy, biomass allocation and vegetative plant growth at three different nitrogen supplies. Planta 190:1–9Google Scholar
  8. Field C, Mooney HA (1986) The photosynthesis-nitrogen relationship in wild plants. In: Givnish TJ (ed) On the economy of plant form and function. Cambridge University Press, Cambridge, pp 25–55Google Scholar
  9. Gebauer G, Melzer A, Rehder H (1984) Nitrate content and nitrate reductase activity in Rumex obtusifolius L. I. Differences in organs and diurnal changes. Oecologia 63:136–142Google Scholar
  10. Grime JP, Hunt R (1975) Relative growth-rate: its range and adaptive significance in a local flora. J Ecol 63:393–422Google Scholar
  11. Handel E van (1967) Determination of fructose and fructose-yielding carbohydrates with cold anthrone. Anal Biochem 19: 193–194Google Scholar
  12. Hofstra RJJ, Lanting L, Visser R de (1985) Metabolism of Urtica dioica as dependent on the supply of mineral nutrients. Physiol Plant 63:13–8Google Scholar
  13. Hunt R, Parsons IT (1974) A computer program for deriving growth functions in plant growth-analysis. J Appl Ecol 11: 297–307Google Scholar
  14. Ingestad T, McDonald AJS (1989) Interaction between nitrogen and photon flux density in birch seedling at steady-state nutrition. Physiol Plant 77:1–11Google Scholar
  15. Isaac RA, Johnson WC (1976) Determination of total nitrogen in plant tissue using a block digester. J Assoc Anal Org Chem 59: 98–100Google Scholar
  16. Lambers H, Poorter H (1992) Inherent variation in growth rate between higher plants: a search for physiological causes and ecological consequences. Adv Ecol Res 23:188–261Google Scholar
  17. Oren R, Schulze E-D (1989) Nutritional disharmony and forest decline: a conceptual model. In: E-D Schulze, OL Lange, R Oren (eds) Ecological Studies 77:425–443 Springer, Berlin HeidelbergGoogle Scholar
  18. Poorter H, Remkes C (1990) Leaf area ratio and net assimilation rate of 24 wild species differing in relative growth rate. Oecologia 83:553–559Google Scholar
  19. Rappoport HF, Loomis FS (1985) Interaction of storage root and shoot in grafted sugarbeet and chard. Crop Sci 25:1079–1048Google Scholar
  20. Sage RF, Pearcy RW (1987) The nitrogen use efficiency of C3 and C4 plants. II. Leaf nitrogen effects on the gas exchange characteristics of Chenopodium album (L.) and Amaranthus retroflexus (L.). Plant Physiol 84:959–963Google Scholar
  21. Schulze W, Schulze E-D, Stadler J, Heilmeier H, Stitt M, Mooney HA (1994) Growth and reproduction of Arabidopsis thaliana in relation to storage of starch and nitrate in wild types, starch-deficient and nitrate-uptake-deficient mutants. Plant Cell Environ 17:795–809Google Scholar
  22. Sonnewald U, Brauer M, Schwaewen A von, Stitt M, Willmitzer L (1991) Transgenic tobacco plants expressing yeast-derived invertase in either the cytosol, vacuole or apoplast: a powerful tool for studying sucrose metabolism and sink/source interactions. Plant J 1:95–106Google Scholar
  23. Steinlein T, Heilmeier H, Schulze E-D (1993) Nitrogen and carbohydrate storage in biennials originating from habitats of different resource availability. Oecologia 93:374–382Google Scholar
  24. Stitt M, Schulze ED (1993) Plant growth, storage and resource allocation — from flux control in a metabolic chain to the whole plant level. In: Schulze E-D (ed) Flux control in biological systems. Academic Press, San Diego, 57–118Google Scholar
  25. Waring RH, McDonald AJS, Larsson S, Ericsson T, Wiren A, Arwidsson E (1985) Differences in chemical composition of plants grown at constant relative growth rates with stable mineral nutrition. Oecologia 66:157–160Google Scholar
  26. Zimmermann R, Oren R, Schulze E-D, Werk KS (1988) Performance of two Picea abies (L.) Karst. stands at different stages of decline. II. Photosynthesis and leaf conductance. Oecologia 76:513–518Google Scholar

Copyright information

© Springer-Verlag 1995

Authors and Affiliations

  • H. A. Mooney
    • 1
  • K. Fichtner
    • 1
  • E.-D. Schulze
    • 1
  1. 1.Lehrstuhl für PflanzenökologieUniversität BayreuthBayreuthGermany

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