Skip to main content
Log in

The carbon isotope ratio of plant organic material reflects temporal and spatial variations in CO2 within tropical forest formations in Trinidad

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

Summary

A method of monitoring and collecting CO2 samples in the field has been developed which has been used to study both temporal and spatial variations in canopy CO2 isotopic signatures in two contrasting tropical forest formations in Trinidad. These have been related to vertical gradients in the carbon isotope ratio (δ13C) of organic material in conjunction with measurements of other environmental parameters. The δ13C of leaf material from two canopies showed a gradient with respect to height, more negative values being found low in the understorey. The deciduous secondary forest, (Simla) showed a difference of 4.6‰ and the semi-evergreen seasonal canopy (Aripo), 2.8‰. The range of δ13C values at Simla was 4‰ less negative than those at Aripo. In order to relate these measurements to the interaction between diffusion or carboxylation limitation, and source CO2 effects, variations in environmental parameters through the canopy have been compared with changes in CO2 partial pressure (P a) and isotopic composition δ13C throughout the day during the dry season. Values of P a20 m above the ground at Aripo varied from 380 vpm at dawn to 340 vpm at midday, at which time the partial pressure 15 cm above the ground was 375 vpm. The CO2 partial pressure did not stabilise during the course of the day, and there was good correlation (r 2=0.82) between δa and P a, with more negative values of δa occuring in the understorey. Diuraal changes of 2‰ were evident at all canopy positions. In the more open canopy at Simla, these gradients were similar, but less marked. Leaf-air vapour pressure deficit (VPD) showed no relationship with height, possibly as a result of minimal water flux from both the soil and the canopy due to low soil water content; VPD was 1.5 kPa higher at midday than dawn. A 3° C temperature gradient between the understorey and upper canopy was observed at Aripo but not in the more open Simla canopy. CO2 partial pressure stabilised for only 4 h in the middle of the day, while other parameters showed no stable period. The proportion of floor respired CO2 reassimilated at Aripo has been calculated as 26%, 19%, and 8% for the periods 0600–1000, 1000–1400, and 1400–1800 hours. In order to quantify source CO2 effects, measurements of the environmental parameters and assimilation rate must be made at all canopy positions and throughout 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

  • Beard JS (1946) The natural vegetation of Trinidad. Oxford Forestry Memoirs, Number 20. Oxford University Press, Oxford

    Google Scholar 

  • Bender MM (1968) Mass spectrometric studies of carbon-13 variations in corn and other grasses. Radiocarbon 10:468–72

    Google Scholar 

  • Christeller JT, Laing WA, Troughton JH (1976) Isotope discrimination by Ribulose-1,5 diphosphate carboxylase. Plant Physiol 57:580–582

    Google Scholar 

  • Ehleringer JR, Field CB, Lin ZF, Kuo CY (1986) Leaf carbon isotope ratio and mineral composition in subtropical plants along an irradiance cline. Oecologia 70:520–26

    Google Scholar 

  • Ehleringer JR, Lin ZF, Field CB, Kuo CY (1987) Leaf isotope ratios of plants from a subtropical monsoon forest. Oecologia 72:109–14

    Google Scholar 

  • Evans JR, Sharkey TD, Berry JA, Farquhar GD (1986) Carbon isotope discrimination measured concurrently with gas exchange to investigate CO2 diffusion in leaves of higher plants. Aust J Plant Physiol 13:281–92

    Google Scholar 

  • Farquhar GD, O'Leary MH, Berry JA (1982) On the relationship between carbon isotope discrimination and intercellular carbon dioxide concentration in leaves. Aust J Plant Physiol 9:121–37

    Google Scholar 

  • Farquhar GD, Ehleringer JR, Hubick KT (1989a) Carbon isotope discrimination and photosynthesis. Annu Rev Plant Physiol Plant Mol Biol 40:503–537

    Google Scholar 

  • Farquhar GD, Hubick KT, Condon AG, Richards RA (1989b) Carbon isotope fractionation and plant-water use efficiency. In: Rundel PW, Ehleringer JR, Nagy KA (eds) Stable Isotopes in Ecological Research. Springer-Verlag, New York, pp 21–40

    Google Scholar 

  • Francey RJ, Hubick KT (1988) Tree-ring carbon-isotope ratios re-examined. Nature 333:712

    Google Scholar 

  • Francey RJ, Gifford RM, Sharkey TD, Weir B (1985) Physiological influences on carbon isotope discrimination in huon pine (Lagarostrobus franklinii). Oecologia 44:241–47

    Google Scholar 

  • Friend AD, Woodward FI, Switsur VR (1989) Field measurements of photosynthesis, stomatal conductance and δ13C along altitudinal gradients in Scotland. Funct Ecol 3:117–22

    Google Scholar 

  • Griffiths H (1991) Applications of stable isotope technology in physiological ecology. Funct Ecol 5:254–269

    Google Scholar 

  • Griffiths H, Broadmeadow MSJ, Borland AM, Hetherington CS (1990) Short term changes in carbon-isotope discrimination identify transitions between C3 and C4 carboxylation during Crassulacean acid metabolism. Planta 181:604–610

    Google Scholar 

  • Keeling CD (1958) The concentration and isotopic abundances of atmospheric carbon dioxide in rural areas. Geochim Cosmochim Acta 13:322–334

    Google Scholar 

  • Keeling CD (1961a) The concentration and isotopic abundances of carbon dioxide in rural and marine air. Geochim Cosmochim Acta 24:277–298

    Google Scholar 

  • Keeling CD (1961b) A mechanism for cyclic enrichment of carbon-12 by terrestrial plants. Geochim Cosmochim Acta 24:299–313

    Google Scholar 

  • Lemon E, Allen LH, Muller L (1970) Carbon dioxide exchange of a tropical rainforest. Part II. BioScience 20:1054–59

    Google Scholar 

  • Marek M, Pirochtova M (1990) Response to the ratio of intercellular CO2 concentration to ambient CO2 concentration (Ci/Ca-ratio) to basic microclimatological factors in an oak-hornbeam forest. Photosynthetica 24:122–129

    Google Scholar 

  • Medina E, Minchin P (1980) Stratification of δ13C values of leaves in Amazonian rain forests. Oecologia 45:377–78

    Google Scholar 

  • Medina E, Montes G, Cuevas E, Roksandic Z (1986) Profiles of CO2 concentration and δ13C values in tropical rainforests of the upper Rio Negro Basin, Venezuela. J Trop Ecol 2:207–17

    Google Scholar 

  • Nobel PS (1983) Biophysical Plant Physiology and Ecology, WH Freeman and Co, San Francisco

    Google Scholar 

  • O'Leary MH (1988) Carbon isotopes in photosynthesis. BioScierice 38:325–336

    Google Scholar 

  • Raven JA, Farquhar GD (1990) The influence of N metabolism and organic acid synthesis on the natural abundance of isotopes of carbon in plants. New Phytol 116:505–529

    Google Scholar 

  • Schleser GH, Jayasekera R (1985) δ13C variations of leaves in forests as an indication of reassimilated CO2 from the soil. Oecologia 65:536–42

    Google Scholar 

  • Smith BN, Oliver J, Chase JB (1973) Effect of growth temperature on carbon isotope ratio in barley, pea and rape. Plant Cell Physiol 14:177–82

    Google Scholar 

  • Sternberg L da SLO'R (1989) A model to estimate carbon dioxide recycling in forests using 13C/12C ratios and concentrations of ambient carbon dioxide. Agric For Meteorol 48:163–173

    Google Scholar 

  • Sternberg LSL, Mulkey SS, Wright SJ (1989) Ecological interpretation of leaf carbon isotope ratios: influence of respired carbon dioxide. Ecology 70:1317–1324

    Google Scholar 

  • Troughton JH, Card K, Bjorkman O (1974) Temperature effects on the carbon isotope ratio of C3, C4 and CAM plants. Carnegie Inst Washington Yearb 73:780–84

    Google Scholar 

  • Van der Merwe NJ, Medina E (1989) Photosynthesis and 13C/12C ratios in Amazonian rain forests. Geochim Cosmochim Acta 53:1091–1094

    Google Scholar 

  • Vogel JC (1978) Recycling of carbon in a forest environment. Oecol Plant 13:89–94

    Google Scholar 

  • Wickman FE (1952) Variations in the relative abundance of the carbon isotopes in plants. Geochim Cosmochim Acta 2:243–254

    Google Scholar 

  • Zimmerman JK, Ehleringer JR (1990) Carbon isotope ratios are correlated with irradiance levels in the Panamanian orchid Catasetum viridiflavum. Oecologia 83:247–249

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Broadmeadow, M.S.J., Griffiths, H., Maxwell, C. et al. The carbon isotope ratio of plant organic material reflects temporal and spatial variations in CO2 within tropical forest formations in Trinidad. Oecologia 89, 435–441 (1992). https://doi.org/10.1007/BF00317423

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00317423

Key words

Navigation