Skip to main content
Log in

Photosynthetic rates in relation to leaf phosphorus content in pioneer versus climax tropical rainforest trees

  • Original Paper
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

In Guyana dense rainforest occurs on intensely weathered acid soils, low in soil phosphorus. To investigate whether low P availability limits photosynthesis of trees growing on these soils more than N does, leaf P and N content, and their relationship with the photosynthetic capacity (A sat, μmol CO2 m-2 s-1) were studied for nine pioneer and climax tree species in a range of light climates. Light environment was described using hemispherical photographs. For both pioneer and climax species, leaf P content (r 2=0.71 and 0.23, respectively) is a more important determinant of A sat than leaf N content (r 2=0.54 and 0.12, respectively). Pioneer species have a higher leaf P and N content than climax species. At similar P or N content, pioneers have a higher A sat than climax species. The saplings studied had a relatively high A sat, considering their low P concentration (15–30 μmol P g-1). All species studied had a constant leaf P and N concentration and photosynthetic capacity across light climates, because specific leaf mass (g m-2) increased similarly with light availability. This acclimation to a change in light environment makes a possible limitation of A sat by P or N independent of light environment.

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

References

  • Bazzaz FA, Pickett STA (1980) Physiological ecology of tropical successions: a comparative review. Annu Rev Ecol Syst 11: 287–310

    Google Scholar 

  • Bradstreet RB (1965) The Kjeldahl method for organic nitrogen. Academic Press, New York

    Google Scholar 

  • Cataldo DA, Haroon M, Schrader LE, Youngs VL (1975) Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid. Commun Soil Sci Plant Anal 6:71–80

    Google Scholar 

  • Chazdon RL, Field CB (1987) Determinants of photosynthetic capacity in six rainforest Piper species. Oecologia 73:222–230

    Google Scholar 

  • De Lucia EH, Schlesinger WH (1991) Resource-use efficiency and drought tolerance in adjacent great basin sierran plants. Ecology 72:51–58

    Google Scholar 

  • Ellsworth DS, Reich PB (1992) Leaf mass per area, nitrogen content and photosynthetic carbon gain in Acer saccharum seedlings in contrasting forest light environments. Funct Ecol 6: 423–435

    Google Scholar 

  • Evans JR (1989) Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia 78:9–19

    Google Scholar 

  • Field C, Mooney HA (1986) The photosynthesis-nitrogen relationship in wild plants. In: Givnish TJ (eds) On the economy of form and function. Cambridge University Press, Cambridge, pp 25–55

    Google Scholar 

  • Houba VJG, Van der Lee JJ, Novazamsky I, Wallinga I (1989) Digestions and extractions. In: Soil and plant analysis, part 7. Plant analysis procedures. Wageningen Agricultural University, Wageningen, pp 12–35

    Google Scholar 

  • Jacob L, Lawlor DW (1992) Dependence of photosynthesis of sunflower and maize leaves on phosphate supply, ribulose-1,5-biphosphate carboxylase/oxygenase activity, and ribulose-1,5-biphosphate pool size. Plant Physiol 98:801–807

    Google Scholar 

  • Jetten VG, Riezebos HT, Hoefsloot F, Van Rossum J (1993) Spatial variability of infiltration and related properties of tropical soils. Earth Surf Process landforms 18:477–488

    Google Scholar 

  • Khan Z, Paul S, Cummings D (1980) Mabura Hill, Upper Demerara Forestry Project. Soils investigation report 1. National Agricultural Research Institute, Mon Repos, Guyana

    Google Scholar 

  • Kirschbaum MUF, Tompkins D (1990) Photosynthetic responses to phosphorus nutrition in Eucalyptus grandis seedlings. Aust J Plant Physiol 17:527–535

    Google Scholar 

  • Lambers H, Poorter H (1992) Inherent variation in growth rate between higher plants: a search for physiological causes and ecological consequences. Adv Ecol Res 23:188–261

    Google Scholar 

  • Mennega EA, Tammens-de Rooij WCM, Jansen-Jacobs MJ (1988) Check-list of woody plants of Guyana. Tropenbos Foundation, Ede

  • Polak AM (1992) Major timber trees of Guyana. A field guide. Tropenbos Foundation, Wageningen

    Google Scholar 

  • Pons TL (1977) An ecophysiological study in the field layer of ash coppice. II. Experiments with Geum urbanum and Cirsium palustre in different light intensities. Acta Bot Neerl 26:29–42

    Google Scholar 

  • Pons TL, Van der Werf A, Lambers H (1993) Photosynthetic nitrogen use efficiency of inherently slow- and fast-growing species: possible explanations for observed differences. In: Roy J, Garnier E (eds) A whole plant perspective on carbon-nitrogen interactions. SPB Academic, The Hague, pp 51–67

    Google Scholar 

  • Raaimakers D, Den Ouden F, Van der Marel M, Boot RGA (1995) Nitrogen and phosphorus as possible limiting factors for tree growth on acid sandy soils in tropical rain forest in Guyana. J Trop Ecol (in press)

  • Rao IM, Terry N (1989) Leaf phosphate status, photosynthesis, and carbon partitioning in sugar beet. Plant Physiol 90:814–819

    Google Scholar 

  • Rao IM, Abadia J, Terry N (1986) Leaf phosphate status and photosynthesis in vivo: changes in light scattering and chlorophyll fluorescence during photosynthetic induction in sugar beet leaves. Plant Sci 44:133–137

    Google Scholar 

  • Reich PB, Schoettle AW (1988) Role of phosphorus and nitrogen in photosynthetic and whole plant carbon gain and nutrient use efficiency in eastern white pine. Oecologia 77:25–33

    Google Scholar 

  • Reich PB, Walters MB, Ellsworth DS, Uhl C (1994) Photosynthesis-nitrogen relations in Amazonian tree species. Oecologia 97:62–72

    Google Scholar 

  • SAS (1991) SAS/STAT user's guide, edn 6.03. SAS Institute, Cary

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. Freeman, San Francisco

    Google Scholar 

  • Stitt M (1990) The flux of carbon between the chloroplast and the cytosol. In: Dennis DT, Turpin HT (eds) Plant physiology, biochemistry and molecular biology. Longman, Harlow, pp 319–339

    Google Scholar 

  • Swaine MD, Whitmore TC (1988) On the definition of ecological species groups in tropical rainforests. Vegetatio 75:81–86

    Google Scholar 

  • Ter Steege H (1993) Hemiphot, a programme to analyze light, light quality and vegetation indices from hemispherical photographs. Tropenbos Foundation, Wageningen

    Google Scholar 

  • Ter Steege H, Jetten V, Polak M, Werger M (1993) Tropical rain forest types and soils of a watershed in Guyana, South America. J. Veg. Sci. 4:705–716

    Google Scholar 

  • Thompson WA, Kriedeman PE, Craig IE (1992a) Photosynthetic response to light and nutrients in sun-tolerant and shade-tolerant rainforest trees. I. Growth, leaf anatomy and nutrient content. Aust J Plant Physiol 19:1–18

    Google Scholar 

  • Thompson WA, Kriedeman PE, Craig IE (1992b) Photosynthetic response to light and nutrients in sun-tolerant and shadetolerant rainforest trees. II. Leaf gas exchange and component processes of photosynthesis. Aust J Plant Physiol 19:19–42

    Google Scholar 

  • Tuohy JM, Prior JAB, Stewart GR (1991) Photosynthesis in relation to leaf nitrogen and phosphorus content in Zimbabwean trees. Oecologia 88:378–382

    Google Scholar 

  • Vitousek PM, Sanford RL (1986) Nutrient cycling in moist tropical forest. Annu Rev Ecol Syst 17:137–167

    Google Scholar 

  • Walters MB, Field CB (1987) Photosynthetic light acclimation in two rainforest Piper species with different ecological amplitudes. Oecologia 72:449–456

    Google Scholar 

  • Walters MB, Kruger EL, Reich PB (1993) Growth, biomass distribution and CO2 exchange of northern hardwood seedlings in high and low light: relationships with successional status and shade tolerance. Oecologia 94:7–16

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Raaimakers, D., Boot, R.G.A., Dijkstra, P. et al. Photosynthetic rates in relation to leaf phosphorus content in pioneer versus climax tropical rainforest trees. Oecologia 102, 120–125 (1995). https://doi.org/10.1007/BF00333319

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00333319

Key words

Navigation