Skip to main content
Log in

Stomatal dynamics and its importance to carbon gain in two rainforest Piper species

I. VPD effects on the transient stomatal response to lightflecks

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

Abstract

The effects of leaf-air vapor pressure deficit (VPD) on the transient and steady-state stomatal responses to photon flux density (PFD) were evaluated in Piper auritum, a pioneer tree, and Piper aequale, a shade tolerant shrub, that are both native to tropical forests at Los Tuxtlas, Veracruz, México. Under constant high-PFD conditions, the stomata of shade-acclimated plants of both species were sensitive to VPD, exhibiting a nearly uniform decrease in gs as VPD increased. Acclimation of P. auritum to high light increased the stomatal sensitivity to VPD that was sufflcient to cause a reduction in transpiration at high VPD's. At low PFD, where gs was already reduced, there was little additional absolute change with VPD for any species or growth condition. The stomatal response to 8-min duration lightflecks was strongly modulated by VPD and varied between the species and growth light conditions. In P. aequale shade plants, increased VPD had no effect on the extent of stomatal opening but caused the rate of closure after the lightfleck to be faster. Thus, the overall response to a lightfleck changed from hysteretic (faster opening than closure) to symmetric (similar opening and closing rates). Either high or low VPD caused gs not to return to the steady-state value present before the lightfleck. At high VPD the value after was considerably less than the value before whereas at low VPD the opposite occurred. Shade-acclimated plants of P. auritum showed only a small gs response to lightflecks, which was not affected by VPD. Under sunfleck regimes in the understory, the stomatal response of P. aequale at low VPD may function to enhance carbon gain by increasing the induction state. At high VPD, the shift in the response enhances water use efficiency but at the cost of reduced 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

References

  • Assmann SM (1988) Enhancement of the stomatal response to blue light by red light, reduced intercellular concentration of CO2, and low vapor pressure differences. Plant Physiol 87:226–231

    Google Scholar 

  • Assmann SM, Grantz DA (1990a) Stomatal response to humidity in sugarcane and soybean: effect of vapor pressure difference on the kinetics of the blue light response. Plant Cell Environment 13:163–169

    Google Scholar 

  • Assmann SM, Grantz DA (1990b) The magnitude of the stomatal response to blue light: modulation by atmospheric humidity. Plant Physiol 93:701–709

    Google Scholar 

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

    Google Scholar 

  • Chazdon RL, Williams K, Field CB (1988) Interactions between crown structure and light environment in five rainforest Piper species. Am Bot 75(10):1459–1471

    Google Scholar 

  • Chiariello NR (1984) Leaf energy balance in the wet lowland tropics. In: Medina E, Mooney HA, Vazquez-Yanes C (eds) Physiological ecology of plants of the wet tropics. Junk, The Hague. pp 85–98

    Google Scholar 

  • Chiarello NR, Field CB, Mooney HA (1987) Midday wilting in a tropical pioneer tree. Func Ecol 1:3–11

    Google Scholar 

  • Davis WJ, Kozlowsky TT (1975) Stomatal responses to changes in light intensity as influenced by plant water stress. Forest Science 21:129–133

    Google Scholar 

  • Doley D, Yates DJ, Unwin GL (1987) Photosynthesis in an australian rainforest tree, Argyrodendron peralatum, during the rapid development and relief of water deficits in the dry season. Oecologia 74:441–449

    Google Scholar 

  • Farquhar GD (1978) Feedforward responses of stomata to humidity. Aust J Plant Physiol 5:787–800

    Google Scholar 

  • Fetcher N (1979) Water relations of five tropical tree species on Barro Colorado Island, Panama. Oecologia 40:229–233

    Google Scholar 

  • Fetcher N, Oberbauer SF, Strain BR (1985) Vegetation effects on the microclimate in lowland tropical forest in Costa Rica. Int J Biometeor 29 (2): 144–156

    Google Scholar 

  • Grantz DA, Zeiger E (1986) Stomatal responses to light and leaf-air water vapor pressure difference show similar kinetics in sugarcane and soybean. Plant Physiol 81:865–868

    Google Scholar 

  • Kirschbaum MUF, Pearcy RW (1988a) Gas exchange analysis of the relative importance of stomatal and biochemical factors in photosynthetic induction in Alocasia macrorrhiza. Plant Physiol 86:782–785

    Google Scholar 

  • Kirschbaum MUF, Pearcy RW (1988b) Gas exchange analysis of the fast phase of photosynthetic induction in Alocasia macrorrhiza. Plant Physiol 87:818–821

    Google Scholar 

  • Kirschbaum MUF, Gross LI, Pearcy RW (1988) Observed and modelled stomatal responses to dynamic light environments in the shade plant Alocasia macrorrhiza. Plant Cell and Environment 11:111–121

    Google Scholar 

  • Knapp AK, Smith WK (1988) Effect of water stress on stomatal and photosynthetic responses in subalpine plants to cloud patterns. Am J Bot 75(6):851–858

    Google Scholar 

  • Knapp AK, Smith WK (1989) Influence of growth form on ecophysiological responses to variable sunlight in subalpine plants. Ecology 70(4):1069–1082

    Google Scholar 

  • Knapp AK, Smith WK (1990) Contrasting stomatal responses to variable sunlight in two subalpine herbs. Am J Bot 72 (2):226–231

    Google Scholar 

  • Mulkey SS, Wright SJ, Smith AP (1991) Drought acclimation of an understory shrub (Psychotria limonensis; Rubiaceae) in a seasonally dry tropical forest in Panama. Am J Bot 78(4):579–587

    Google Scholar 

  • Oberbauer SF, Strain BR, Riechers GH (1987) Field water relations of a wet tropical forest tree Pentaclethra macroloba (Mimosaceae). Oecologia 71:369–374

    Google Scholar 

  • Pearcy RW (1990) Sunflecks and photosynthesis in plant canopies. Annu Rev Plant Physiol Plant Mol Biol 41:421–453

    Google Scholar 

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

    Google Scholar 

  • Pearcy RW (1987) Photosynthetic gas exchange responses of Australian tropical forest trees in canopy, gap and understory microenvironments. Funct Ecol 1:169–178

    Google Scholar 

  • Pfitsch WA, Pearcy RW (1989) Steady-state and dynamic photosynthetic response of Adenocaulon bicolor (Asteraceae) in its redwood forest habitat. Oecologia 80:471–476

    Google Scholar 

  • Robichaux RH, Rundel PW, Stemmermann L, Canfield JE, Morse SR, Friedman WE (1984) Tissue water deficits and plant growth in wet tropical environments. In: Medina E, Mooney HA, Vazquez-Yanes C (eds) Physiological ecology of plants of the wet tropics. Junk, The Hague. pp 99–112

    Google Scholar 

  • Schulze E-D, Hall AE (1982) Stomatal responses, water loss and CO2 assimilation rates of plants in contrasting environments. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Encyclopedia of Plant Physiology NS, Springer, Berlin, 12B: 181–230

    Google Scholar 

  • Tinoco-Ojanguren C, Pearcy RW (1992) Dynamics stomatal behavior and its role in carbon galn during lightflecks of a gap phase and an understory Piper species acclimated to high and low light. Oecologia 92:222–228

    Google Scholar 

  • Tinoco-Ojanguren C, Pearcy RW (1993) Stomatal dynamics and its importance to carbon gain in two rainforest Piper species. II. Stomatal versus biochemical limitations during photosynthetic induction. Oecologia 94:395–402

    Google Scholar 

  • Willis AJ, Balasubramaniam S (1968) Stomatal behavior in relation to rates of photosynthesis and transpiration in Pelargonium. New Phytol 67:265–285

    Google Scholar 

  • Woods DB, Turner NC (1991) Stomatal responses to changing light by four tree species of varying shade tolerance. New Phytol 70:77–84

    Google Scholar 

  • Young DR, Smith WK (1979) Influence of sunflecks on the temperature and water relations of two subalpine understory congeners. Oecologia 43:195–205

    Google Scholar 

  • Zeiger E (1990) Light perception in guard cells. Plant Cell and Environment 13:739–747

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tinoco-Ojanguren, C., Pearcy, R.W. Stomatal dynamics and its importance to carbon gain in two rainforest Piper species. Oecologia 94, 388–394 (1993). https://doi.org/10.1007/BF00317114

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00317114

Key words

Navigation