Skip to main content
Log in

The influence of a decrease in irradiance on photosynthetic carbon assimilation in leaves of Spinacia oleracea L.

  • Published:
Planta Aims and scope Submit manuscript

Abstract

When leaves of Spinacia oleracea L. were subjected to a decrease from a saturating to a limiting irradiance, photosynthetic carbon assimilation exhibited a pronounced lag. This comprised a postlower-illumination CO2 burst (Vines et al. 1982, Plant Physiol. 70, 629–631) and a slow increase in the rate of carbon assimilation to the new lower steady-state rate. The latter phenomenon was distinguishable from the former because it was present in leaves when photorespiration was inhibited by high concentrations of CO2 or by 2% O2. A lag which followed a decrease in irradiance was also evident in leaves of Zea mays in air or in isolated spinach protoplasts photosynthesising in high CO2. The lag was not stomatal in origin. The origin of the lag which followed the decrease in irradiance was investigated. Measurements of total 14CO2 fixation and 14C incorporated into sucrose during the transition in irradiance showed that sucrose synthesis displayed an overshoot during the transient which accounted for all of the carbon fixed during the first 90 s of the transition period. The behaviour of hexose phosphates in the intact leaf and in the cytosol was inconsistent with their supporting sucrose synthesis during the transient. It is concluded that the overshoot in sucrose synthesis imposes a drain on chloroplast intermediates which contributes to the temporary lag in the rate of carbon assimilation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

Ci:

intercellular concentration of CO2

References

  • Arnon, D.I. (1949) Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris. Plant Physiol. 24, 1–15

    Google Scholar 

  • Cowan, I.R. (1977) Stomatal behaviour and environment. Adv. Bot. Res. 4, 117–228

    Google Scholar 

  • Decker, J.P. (1955) A rapid, post-illumination deceleration of respiration in green leaves. Plant Physiol. 30, 82–84

    Google Scholar 

  • Dietz, K-J. Heber, U. (1984) Rate-limiting factors in leaf photosynthesis. I. Carbon fluxes in the Calvin cycle. Biochim. Biophys. Acta. 767, 432–443

    Google Scholar 

  • Gross, L.J., Chabot, B.F. (1979) Time course of photosynthetic response to changes in incident light energy. Plant Physiol. 63, 1033–1038

    Google Scholar 

  • Gross, L.J. (1982) Photosynthetic dynamics in varying light environments: a model and its application to whole leaf carbon gain. Ecology 63, 84–93

    Google Scholar 

  • Harris, G.C., Cheesbrough, J.K., Walker, D.A. (1983) Measurement of CO2 and H2O vapour exchange in spinach leaf discs. Effects of orthophosphate. Plant Physiol. 71, 102–107

    Google Scholar 

  • Jones, D.A., Smith, A.M., Woolhouse, H.W. (1983) An apparatus for pulse and pulse-chase experiments with 14CO2 on attached leaves with known, steady-state rates of photosynthesis. Plant Cell Environ. 6, 161–166

    Google Scholar 

  • Leegood, R.C., Edwards, G.E., Walker, D.A. (1981) Chloroplasts and protoplasts. In: Techniques in bioproductivity and photosynthesis, Coombs, J., Hall, D.O., eds. Pergamon Press, Oxford London

    Google Scholar 

  • Leegood, R.C., Furbank, R.T. (1984) Carbon metabolism and gas exchange in leaves of Zea mays L. Changes in CO2 fixation, chlorophyll a fluorescence, and metabolite levels during photosynthetic induction. Planta 162, 450–456

    Google Scholar 

  • Lowry, O.H., Passonneau, J.V. (1972) A flexible system of enzymatic analysis. Academic Press, New York London

    Google Scholar 

  • McCree, K.J., Loomis, R.S. (1969) Photosynthesis in fluctuating light. Ecology 50, 422–428

    Google Scholar 

  • Mourioux, G., Douce, R. (1981) Slow passive diffusion of orthophosphate between intact isolated chloroplasts and suspending medium. Plant Physiol. 67, 470–473

    Google Scholar 

  • Pollard, D.F.W. (1970) The effect of rapidly changing light on the rate of photosynthesis in large tooth aspen (Populus grandidentata). Can. J. Bot. 48, 823–829

    Google Scholar 

  • Steeman-Nielsen, E. (1949) A reversible inactivation of chlorophyll in vivo. Physiol. Plant. 2, 247–265

    Google Scholar 

  • Stitt, M., ap Rees, T. (1978) Pathways of carbohydrate oxidation in leaves of Pisum sativum and Triticum aestivum. Phytochemistry 17, 1251–1256

    Google Scholar 

  • Stitt, M., Wirtz, W., Heldt, H.W. (1983) Regulation of sucrose synthesis, by cytoplasmic fructose bisphosphatase and sucrose phosphate synthase in varying light and carbon dioxide. Plant Physiol. 72, 767–774

    Google Scholar 

  • Vines, H.M., Armitage, A.M., Chen, S., Tu, Z., Black, C.C. (1982) A transient burst of CO2 from Geranium leaves during illumination at various light intensities as a measure of photorespiration. Plant Physiol. 70, 629–631

    Google Scholar 

  • Vines, H.M., Tu, Z., Armitage, A.M., Chen, S., Black, C.C. (1983) Environmental responses of the post-lower illumination CO2 burst as related to leaf photorespiration. Plant Physiol. 73, 25–30

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Prinsley, R.T., Hunt, S., Smith, A.M. et al. The influence of a decrease in irradiance on photosynthetic carbon assimilation in leaves of Spinacia oleracea L.. Planta 167, 414–420 (1986). https://doi.org/10.1007/BF00391348

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00391348

Key words

Navigation