Skip to main content
Log in

Photosynthetic acclimation to light in juveniles of two cloud forest tree species

  • Original Article
  • Published:
Trees Aims and scope Submit manuscript

Abstract

The photosynthetic response of juveniles of Decussocarpus rospigliosii, an emergent primary forest species and shade tolerant in its juvenile stages and Alchornea triplinervia, a gap-colonizing species of tropical cloud forest in Venezuela was studied. Daily courses of microenvironmental variables and gas exchange under contrasting light conditions (gap and understory) were carried out in their natural environment and transplanted to different light regimes (shade and sun) in the field. The photosynthetic response and some anatomical characteristics of plants from different treatments were analyzed in the laboratory. Photosynthetic rates were low for both species, and were negative during some diurnal periods, related to the low photosynthetically active radiation levels obtained at both gap (6% of total radiation) and understory (2%). A. triplinervia shows higher rates (1.5–3.0 μmolm-2 -1) than D. rospigliosii (0.7–1.1 μmolm-2s-1). Both species showed increased photosynthetic rates when grown in gaps. A. triplinervia did not adjust its maximum photosynthetic rates to the prevailing light conditions. In contrast, D. rospigliosii responded to increased light levels. Both species showed low light compensation points when grown under total shade. There was a partial stomatal closure generally during midday in D. rospigliosii. A. triplinervia presented lower leaf conductances, transpiration rates and lesser stomatal control. Some leaf anatomical characteristics, in both species, were affected by variations in the light regime (i.e. increased leaf thickness, leaf specific weight and stomatal density). These results suggest that both species have the ability to respond to variations in their natural light environments, therefore maintaining a favorable carbon balance during the day.

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

  • Añez MA (1987) Relaciones hídricas y nutricionales en especies arbóreas de un bosque nublado, a lo largo de un gradiente sucesional. Master Thesis. IVIC, Caracas. Venezuela

    Google Scholar 

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

    Google Scholar 

  • Bazzaz FA (1984) Dynamics of wet tropical forest and their species strategies. In: Medina E, Mooney HA, Vazquez-Yanes C (eds) Physiological ecology of plants of the wet tropics. Dr. W. Junk, The Hague, pp 233–243

    Google Scholar 

  • Bazzaz FA, Carlson RW (1982) Photosynthetic acclimation to variability in the light environment of early and late successional species. Oecologia 54: 313–316

    Google Scholar 

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

    Google Scholar 

  • Boardman NK (1977) Comparative photosynthesis of sun and shade plants. Annu Rev Plant Physiol 28: 355–377

    Google Scholar 

  • von Caemmerer S, Farquhar GD (1981) Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153: 376–387

    Google Scholar 

  • Chabot BF, Jurik TW, Chabot JF (1979) Influence of instantaneous and integrated light-flux density on leaf anatomy and photosynthesis. Am J Bot 66: 940–945

    Google Scholar 

  • Chazdon RL (1988) Sunflecks and their importance to forest understory palms. J Ecol 74: 995–1012

    Google Scholar 

  • Chazdon RL, Fetcher N (1984) Photosynthetic light environments in a lowland tropical rain forest in Costa Rica. J Ecol 72: 553–564

    Google Scholar 

  • Clark DA, Clark DB (1987) Análisis de la regeneración de árboles del dosel en un bosque muy húmedo tropical: aspectos teóricos y prácticos. Rev Biol Trop 35: 41–45

    Google Scholar 

  • Denslow JS (1980) Gap partitioning among tropical rain forest trees. Biotropica 12: 47–55

    Google Scholar 

  • Denslow JS (1987) Tropical rainforest gaps and the tree species diversity. Annu Rev Ecol Syst 18: 431–451

    Google Scholar 

  • Edwards WRN, Jarvis PG (1982) Relations between water content, potential and permeability in stems of conifers. Plant Cell Environ 5: 271–277

    Google Scholar 

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

    Google Scholar 

  • Fetcher N, Strain BR, Oberbauer SF (1983) Effects of light regime on growth, leaf morphology, and water relations of seedlings of two species of tropical trees. Oecologia 58: 314–319

    Google Scholar 

  • Fetcher N, Oberbauer SF, Rojas G, Strain BR (1987) Efectos del régimen de luz sobre la fotosíntesis y el crecimiento en plántulas de árboles de un bosque lluvioso tropical de Costa Rica. Rev Biol Trop 35: 97–110

    Google Scholar 

  • García-Núñez C (1992) Efecto del ambiente de luz en la respuesta fotosintética, anatomía foliar y relaciones hídricas en plántulas de dos especies arbóreas de la selva nublada de La Carbonera. Masters Thesis. Facultad de Ciencias, ULA. Mérida, Venezuela

    Google Scholar 

  • Granier A, Huc R, Collin F (1992) Transpiration and stomatal conductance of two rain forest species growing in plantations (Simamba amara and Goupia glabra) in French Guyana. Ann Sci For 49: 17–24

    Google Scholar 

  • Grieu P, Guehl JM, Aussenac G (1988) The effect of soil and atmospheric drought on photosynthesis and stomatal control of gas exchange in three coniferous species. Physiol Plant 73: 97–104

    Google Scholar 

  • Grubb PJ (1977) Control of forest growth and distribution on wet tropical mountains: with special reference to mineral nutrition. Annu Rev Ecol Syst 8: 83–107

    Google Scholar 

  • Hartshorn GS (1978) Tree falls and tropical forest dynamics. In: Tomlinson PB, Zimmerman MH (eds) Tropical trees as living systems. Cambridge University Press, Cambridge, pp 617–638

    Google Scholar 

  • Hartshorn GS (1980) Neotropical forest dynamics. Biotropica 12: 23–30

    Google Scholar 

  • Huber O (1986) Las selvas nubladas de Rancho Grande: observaciones sobre su fisionomfa, estructura y fenología. In: Huber O (eds). La Selva Nublada de Rancho Grande. Parque Nacional “Henri Pittier”. Fondo Editorial Acta Cientfffca, Caracas, pp 131–170

    Google Scholar 

  • Huc R, Guehl JM (1989) Environmental control of CO2 assimilation rate and leaf conductance in two species of the tropical rain forest of French Guiana (Jacaranda copaia D. Don and Eperua falcata Aubl.). Ann Sci for 46S; Forest Tree Physiology 443–447

  • Johansen DA (1940) Plant microtechnique. Macgraw Hill, New York, pp 522

    Google Scholar 

  • Jurik TW, Chabot JF, Chabot BF (1979) Ontogeny of photosynthetic performance in Fragaria virginiana under changing light regimes. Plant Physiol 63: 542–547

    Google Scholar 

  • Kaufmann MR (1976) Stomatal response of Engelmann spruce to humidity, ligth, and water stress. Plant Physiol 57: 898–801

    Google Scholar 

  • Kwesiga FR, Grace J, Sandford AP (1986) Some photosynthetic characteristics of tropical timber trees as affected by the light regime during growth. Ann Bot 58: 23–32

    Google Scholar 

  • Lamprecht H, Liscano C (1957) Estudios sobre la regeneratión del Podocarpus rospigliosii Pilger y su desarrollo en la juventud. Instituto Forestal Latinoamericano de Investigatión y Capacitación Forestal. Boletin no. 2, 41–72

  • Lamprecht H, Veillón JP (1957) La Carbonera. El Farol 18 158: 17–24

    Google Scholar 

  • Langenheim JH, Osmond CB, Brooks A, Ferrar PJ (1984) Photosynthetic responses to light in seedlings of selected Amazonian and Australian rainforest tree species. Oecologia 63: 215–224

    Google Scholar 

  • Landsberg JJ (1977) Some useful equations for biological studies. Exp Agric 13: 273–286

    Google Scholar 

  • Lebron ML (1980) Physiological plant ecology: some contributions to the understanding of secondary succession in tropical lowland rainforest. Biotropica 12: 23–30

    Google Scholar 

  • Loach K (1967) Shade tolerance in tree seedlings. I. Leaf photosynthesis and respiration in plants raised under artificial shade. New Phytol 66: 607–621

    Google Scholar 

  • Medina E (1986) Forest, savannas and montane tropical environments. In: Baker NR, Long SP (eds) Photosynthesis in contrasting environments. Elsevier Science, Amsterdam, pp 139–171

    Google Scholar 

  • Meinzer F, Goldstein G, Jaimes M (1984) The effect of atmospheric humidity on stomatal control of gas exchange in two tropical coniferous species. Can J Bot 62: 591–595

    Google Scholar 

  • Mooney HA, Field CB, Vazquez-Yánez C, Chu C (1983) Environmental control on stomatal conductance in a shrub of the humid tropics. Proc Natl Acad Sci USA 80: 1295–1297

    Google Scholar 

  • Mooney HA, Field C, Vazquez-Yanes C (1984) Photosynthetic characteristics of wet tropical forest plants. Medina E, Mooney HA, Vazquez-Yanez C (eds) Physiological ecology of plants of the wet tropics. Dr. W. Junk, The Hague, pp 113–128

    Google Scholar 

  • Müller L (1961) Un aparato de microKjeldahl simple para análisis rutinarios rápidos de materiales vegetales. Turrialba 11: 17–25

    Google Scholar 

  • Oberbauer SF, Strain BR (1984) Photosynthesis and successional status of Costa Rican rain forest trees. Photosynthesis Res 5: 227–232

    Google Scholar 

  • Orians GH (1982) The influence of tree-falls in tropical forest in tree species richness. Trop Ecol 23: 255–279

    Google Scholar 

  • Pearcy RW, Calkin HW (1983) Carbon dioxide exchange of C3 and C4 tree species in the understory of Hawaiian forest. Oecologia 58: 26–32

    Google Scholar 

  • Pearcy RW, Chazdon RL, Kirschbaum MUF (1987) Photosynthetic utilization of light flecks by tropical forest plants. In: Biggens J (ed) Progress in photosynthesis research, vol IV. Martinus Nijhoff, Dordrecht, pp 257–260

    Google Scholar 

  • Popma P, Bongers F (1988) The effect of canopy gaps on growth and morphology of seedlings of rain forest species. Oecologia 75: 625–632

    Google Scholar 

  • Rada F, González J, Azócar A, Briceño B, Jaimez R (1992) Net photosynthesis-leaf temperature relations in plant species with different height along an altitudinal gradient. Acta Oecologica 13: 535–542

    Google Scholar 

  • Reich PB, Uhl C, Walters MB, Ellsworth DS (1991) Leaf lifespan as a determinant of leaf structure and function among 23 Amazonian tree species. Oecologia 86: 16–24

    Google Scholar 

  • Sanchez-Coronado ME, Rincon E, Vazquez-Yanez C (1990) Growth responses of three contrasting Piper species growing under different light conditions. Can J Bot 68: 1182–1186

    Google Scholar 

  • Sarmiento G, Monasterio M, Azócar A, Castellano E, Silva J (1971) Estudio integral de la cuenca de los nos Chama y Capazón. Subproyecto N∘ III. Vegetatión Natural. U. L. A. Facultad de Ciencias. Mérida, Venezuela

    Google Scholar 

  • Sims DA, Pearcy RW (1989) Photosynthetic characteristics of a tropical forest understory herb. Alocasia macrorrhiza, and a related crop species. Colocasia esculenta, grown in contrasting light environments. Oecologia 79: 53–59

    Google Scholar 

  • Steyermark J, Huber O (1978) Flora del Avila. Publicatión Especial de la Sociedad Venezolana de Ciencias Naturales, Caracas

    Google Scholar 

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

    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 

  • Whitmore TC (1978) Gaps in forest canopy. In: Tomlinson PB, Zimmerman MH (eds) Tropical trees as living systems. Cambridge University Press, Cambridge pp 639–655

    Google Scholar 

  • Whitmore TC (1989) Canopy and gaps and the two major groups of forest trees. Ecology 70: 536–538

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

García-Núñez, C., Azócar, A. & Rada, F. Photosynthetic acclimation to light in juveniles of two cloud forest tree species. Trees 10, 114–124 (1995). https://doi.org/10.1007/BF00192192

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00192192

Key words

Navigation