Skip to main content

Possible Effects of Climate Change on Plant/Herbivore Interactions in Moist Tropical Forests

  • Chapter

Abstract

The interactions between plants and herbivores are key determinants of community structure world wide. Their role is particularly important in lowland tropical rain forests where rates of herbivory are higher, plants are better defended chemically and physically, and herbivores have specialized diets. In contrast to the temperate zone, most of the herbivory in the tropics occurs on ephemeral young leaves (>70%), which requires herbivores to have finely tuned host-finding abilities. As a consequence of these tight ecological and evolutionary linkages, the interplay between plants and herbivores in the tropics may be more susceptible to perturbations of climate change.

Increases in global temperature, atmospheric CO2, and the length of the dry season are all likely to have ramifications for plant/herbivore interactions in the tropics. Here I extrapolate from our current and incomplete understanding of the mechanisms regulating plant/herbivore interactions and present a scenario for possible trends under a changing climate. Although elevated CO2 tends to enhance plant growth rates, the larger effects of increased drought stress will probably result in lower growth. In atmospheres experimentally enriched in CO2, the nutritional quality of leaves declines substantially due to a dilution of nitrogen by 10–30%. This response is buffered in plant species associated with nitrogen fixers. Elevated CO2 should also cause a slight decrease in nitrogen-based defenses (e.g., alkaloids) and a slight increase in carbon-based defenses (e.g., tannins). The most dramatic and robust predicted effect of climate change is on rates of herbivory. Lower foliar nitrogen due to CO2 fertilization of plants causes an increase in consumption per herbivore by as much as 40%, and unusually severe drought appears to cause herbivore populations to explode. In areas where elevated CO2 is combined with drying, rates of herbivoiy may rise 2–4 fold. The frequency of insect outbreaks is also expected to increase. Higher herbivory should further reduce plant growth rates, perhaps favoring plant species that are well-defended or fix nitrogen. The predicted increase in the number of herbivores is primarily due to relaxed pressure from predators and parasitoids. Elevated temperatures may increase herbivore developmental times, affording them partial escape from discovery by natural enemies, and drought appears to decimate parasitoid populations. The expected decline in parasitoid numbers may be due to direct effects of dry season drought or to the relative scarcity of herbivores during that period. As a consequence, the relative abundance of species will change, and overall biodiversity should decline.

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

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   169.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Aide, T.M.: 1988. Herbivoiy as a selective agent on the timing of leaf production in a tropical understory community. Nature 336, 574–575

    Article  Google Scholar 

  • Aide, T.M.: 1991. Synchronous leaf production and herbivory in juveniles of Gustavia superba. Oecologia 88, 511–514.

    Google Scholar 

  • Aide, T.M.: 1993. Patterns of leaf development and herbivory in a tropical understory community. Ecology 74, 455–466.

    Article  Google Scholar 

  • Aide, T.M. and Londono, E.C.: 1989. The effects of rapid leaf expansion on the growth and survivorship of a lepidopteran herbivore. Oikos 55, 66–70.

    Article  Google Scholar 

  • Aide, T.M. and Zimmerman, J.K.: 1990. Patterns of insect herbivory, growth, and survivorship in juveniles of a neotropical liana. Ecology 71, 1412–1421.

    Article  Google Scholar 

  • Aiello, A.: 1992. Dry season strategies of two Panamanian butterfly species, Anartia fatima (Nymphalinae) and Pie re IIa luna luna (Satyrinae) (Lepidoptera: Nymphalidae). pp 573–575 in Quintero Arias, D. and Aiello, A. (eds). Insects of Panama and Mesoamerica: Selected Studies. Oxford University Press.

    Google Scholar 

  • Anderson, J.A.R.: 1961. The destruction of Shorea albida forest by an unidentified insect. Empire Forestry Review 40, 19–29.

    Google Scholar 

  • Arnone, J.A., III.: 1996, Predicting responses of tropical plant communities to elevated CO2: Lessions from experiments with model ecosystems, pp 101–121 in Körner, Ch. and Bazzaz, F.A. (eds) Carbon dioxide, populations and communities. Academic Press, San Diego.

    Chapter  Google Scholar 

  • Arnone, J.A., Ill and Körner, Ch.: 1995, Soil and biomass carbon pools in model communities of tropical plants under elevated CO2. Oecologia 104, 61–71.

    Article  Google Scholar 

  • Arnone, J.A., III, Zaller, J.G., Ziegler, C., Zandt, H. and Körner, Ch.: 1995, Leaf quality and insect herbivory in model tropical plant communities after long-term exposure to elevated atmospheric CO2, Oecologia 104, 72–78.

    Article  Google Scholar 

  • Ayres, M.P.: 1993. Plant defense, herbivory and climate change, pp 75–94 in Kareiva, P.M, Kingsolver, J.G.and Huey, R.B. (eds) Biotic Interactions and Global Change. Sinauer Associates, Sunderland, MA.

    Google Scholar 

  • Barone, J. A.: 1997. Host-specificity of folivorous insects in a moist tropical forest. J Animal Ecol (in press).

    Google Scholar 

  • Basset, Y.: 1992. Host specificity of arboreal and free-living insect herbivores in rainforests. Biol J Linnean Soc 47:, 155–133.

    Article  Google Scholar 

  • Bazzaz, F.A.: 1990. The response of natural ecosystems to the rising C02 levels. Ann Rev Ecol & Syst 21, 167–196.

    Article  Google Scholar 

  • Bazzaz, F.A. and Garbutt, K.: 1988. The response of annuals in competitive neighborhoods: effects of elevated C02. Ecology 69, 937–946.

    Article  Google Scholar 

  • Bernays, E.A., Bright, K.L., Gonzales, N. and Angel, J.: 1994. Dietary mixing in a generalist herbivore: Tests of two hypotheses. Ecology 75, 1997–2006.

    Article  Google Scholar 

  • Bernays, E.A.: 1997, Feeding by lepidopteran larvae is dangerous. Ecol Ent 22, 121–123.

    Article  Google Scholar 

  • Berryman, A.A., Stenseth, N. Chr. and Isaev, A.S.: 1987. Natural regulation of herbivorous forest insect populations. Oecologia 71, 174–184.

    Article  Google Scholar 

  • Biyant, J.P., Chapin, F.S. and Klein, D.R.: 1983. Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 40, 357–368.

    Article  Google Scholar 

  • Carlson, R.W. and Bazzaz, F.A.: 1980. The effects of elevated C02 concentrations on growth, photosynthesis, transpiration and water use efficiency of plants, pp 609–623 in Singh, J.J. and Deepak, A. (eds) Environmental and Climatic Impact of Coal Utilization. Academic Press, New York.

    Google Scholar 

  • Chazdon, R.L. and Fetcher, N.: 1984. Light environments of tropical forests, pp 27–36 In Medina E., Mooney, H.A. and Vazquez-Yanes, C. (eds) Physiological Ecology of Plants of the Wet Tropics. Junk, Boston, MA.

    Chapter  Google Scholar 

  • Coley, P.D.: 1983. Herbivory and defensive characteristics of tree species in a lowland tropical forest. Ecol Mongr 53, 209–233

    Article  Google Scholar 

  • Coley, P.D., Bryant, J.P., and Chapin, F.S., III.: 1985. Resource availability and plant anti-herbivore defense. Science 230, 895–899

    Article  CAS  Google Scholar 

  • Coley, P.D. and Aide, T.M.: 1991. Comparison of herbivory and plant defenses in temperate and tropical broad-leaved forests, pp 25–49 in Price, P.W., Lewinsohn, T.M., Wilson Fernandes, G.W. and Benson, W.W. (eds) Plant-animal Interactions: Evolution Ecology in Tropical and Temperate Regions. John Wiley and Sons, NY, pp. 25–49.

    Google Scholar 

  • Coley, P.D. and Kursar, T.A.: 1996. Anti-herbivore defenses of young tropical leaves: Physiological constraints and ecological tradeoffs, pp 305–336 in Smith, A.P., Mulkey, S.S. and Chazdon, R.L. (eds) Tropical Forest Plant Ecophysiology, Chapman and Hall, NY.

    Chapter  Google Scholar 

  • Coley, P.D. and Barone, J.A.: 1996, Herbivory and plant defenses in tropical forests. Ann Rev Ecol & Syst 27, 305–335.

    Article  Google Scholar 

  • Condit, R., Hubbell, S.P., and Foster, R.B.: 1992. Stability and change of a neotropical moist forest over a decade. Bioscience 42, 822–828.

    Article  Google Scholar 

  • Condit, R., Hubbell, S.P., and Foster, R.B.: 1995. Mortality rates of 205 neotropical tree species and the responses to a severe drought. Ecological Monographs 65, 419–439

    Article  Google Scholar 

  • Condit, R.: 1998. Ecological implications of changes in drought patterns: Shifts in forest composition in Panama. Clim. Change 39(this volume)

    Google Scholar 

  • Crawley, M.J., 1983. Herbivory: The Dynamics of Animal-Plant Interactions, Blackwell, Oxford.

    Google Scholar 

  • Crawley, M.J.: 1989. The responses of terrestrial ecosystems to global climate change. ppl41–164 in MacDonald, G.J. and Sertorio, L. (eds) Global Climate and Ecosystem Change, NATO ASI Series B, Vol 240.

    Google Scholar 

  • Fajer, E.D.: 1989. The effects of enriched C02 atmospheres on plant-insect herbivore interactions: growth responses of larvae of the specialist butterfly, Junonia coenia (Lepidoptera: Nymphalidae). Oecologia 81, 514–520.

    Article  Google Scholar 

  • Fajer, E.D., Bowers, M.D., and Bazzaz, F.A.: 1989. The effects of enriched C02 atmospheres on plant-insect herbivore interactions. Science 243, 1198–1200.

    Article  CAS  Google Scholar 

  • Fajer, E.D., Bowers, M.D., and Bazzaz, F.A.: 1991. The effects of enriched C02 atmospheres on the buckeye butterfly Junonia coenia. Ecology 72, 571–574.

    Google Scholar 

  • Gershenzon, J.: 1984. Changes in the levels of plant secondary metabolites under water and nutrient stress. Ree Adv Phytochem 18, 273–320.

    CAS  Google Scholar 

  • Hemming, J.D.C. and Lindroth, R.L.: 1995. Intraspecifrc variation in aspen phytochemistry: effects on performance of gypsy moths and forest test caterpillars. Oecologia 103, 79–88.

    Article  Google Scholar 

  • Hubbell, S.P. and Foster, R.B.: 1990. Structure, dynamics and equilibrium status of old-growth forest on Barro Colorado Island, pp 522–541 in Gentry, A.H. (ed) Four Neotropical Rainforest, Yale University Press, New Haven.

    Google Scholar 

  • Hulme, M. and Viner, D.: 1995. A climate change scenario for assessing the impact of climate change of tropical rain forests. WWF report.

    Google Scholar 

  • Johnson, R.H., and Lincoln, D.E.: 1990. Sagebrush and grasshopper responses to atmospheric carbon dioxide concentration. Oecologia 84, 103–110.

    Article  Google Scholar 

  • Johnson, R.H., and Lincoln, D.E.: 1991. Sagebrush carbon allocation patterns and grasshopper nutrition: the influence of C02 enrichment and soil mineral limitation. Oecologia,1 127–134.

    Article  Google Scholar 

  • Julkunen-Tiitto, R. Tahvanainen, J. and Silvola, J.: 1993, Increased CO2 and nutrient status changes affect phytomass and production of defensive chemicals in Salix myrsinifolia (Salisb). Oecologia 95, 495–498.

    Google Scholar 

  • Kinney, K.K., Lindroth, R.L., Jung, S.M., and Nordheim, E.V.: 1997. Effects of C02 and N03“ availability on deciduous trees: phytochemistry and insect performance. Ecology 78, 215–230.

    Google Scholar 

  • Körner, Ch.: 1993. C02 fertilization: the great uncertai778nty in future vegetation development, pp 53–70 in Solomon, A.M. and Shugart, H.H. (eds). Vegetation Dynamics and Global Change. Chapman and Hall, NY.

    Chapter  Google Scholar 

  • Körner, Ch.: 1996. The response of complex multispecies systems to elevated C02. in Walker, B.H., Steffen, W.L. (eds) Global Change and Terrestrial Ecosystems. Cambridge University Press, Cambridge.

    Google Scholar 

  • Körner, Ch., and Arnone, J.A. III.: 1992. Responses to elevated carbon dioxide in artificial tropical ecosystems. Science 257, 1672–1675.

    Article  Google Scholar 

  • Kozlowski, T.T., Kramer, P.J., and Pallardy, S.G.: 1991. The Physiological Ecology of Woody Plants, Academic Press, NY

    Google Scholar 

  • Landsberg, J. and Smith, M.S.: 1992, A functional scheme for predicting the outbreak potential of herbivorous insects under global atmospheric change, Australian J of Botany 40, 565–577.

    Article  Google Scholar 

  • Leigh, E.G. Jr., Windsor, D.M., Rand, A.S. and Foster, R.B.: 1990, The impact of the “El Nino” drought of 1982–1983 on a Panamanian semideciduous forest, pp 473–486 in Glynn, P.W. (ed) Global Ecological Consequences of the 1982–1983 El Nino-Southern Oscillation. Elsevier Oceanography Series.

    Google Scholar 

  • Levin, D.A.: 1976. Alkaloid-bearing plants: An ecogeographic perspective. AmerNat 110, 261–284.

    Article  Google Scholar 

  • Lincoln, D.E. and Couvet, D.: 1989. The effect of carbon supply on allocation to allelochemicals and caterpillar consumption of peppermint. Oecologia 78, 112–114.

    Article  Google Scholar 

  • Lincoln, D.E., Couvet, D., and Sionit, N.: 1986. Response of an insect herbivore to host plants grown in enriched carbon dioxide atmospheres. Oecologia 69, 556–560.

    Article  Google Scholar 

  • Lincoln, D.E., Sionit, N. and Strain, B.R.: 1984. Growth and feeding responses of Pseudoplusia includens (Lepidoptera: Noctuidae) to host plants in controlled carbon dioxide atmospheres. Environ Entomol 13, 1527–1530.

    CAS  Google Scholar 

  • Lincoln, D.E., Fajer, E.D. and Johnson, R.H.: 1993. Plant-insect herbivore interactions in elevated C02 environments. Trends in Ecol & Evol 8, 64–68.

    Article  CAS  Google Scholar 

  • Lindroth, R.L., Kinney, K.K., and Platz, C.L.: 1993. Responses of deciduous trees to elevated atmospheric C02: productivity, phytochemistry and insect performance. Ecology l A, 763–777.

    Google Scholar 

  • Lindroth, R.L., Arteel, G.E. and Kinney, K.K.: 1995, Reponses of three saturniid species to paper birch grown under enriched CO2 atmospheres. Func Ecol 9, 306–311.

    Article  Google Scholar 

  • Lovelock, C.E., Kyllo, D., Popp, M., Isopp, H., Virgo, A., and Winter, K.: 1997. Symbiotic vesicular-arbuscular mycorrhizae influence maximum rates of photosysnthesis in tropical tree seedlings grown under elevated CO2. Aust J Plant Physiol 24, 185–194.

    Article  CAS  Google Scholar 

  • Malcolm, J.R.: 1991. The small mammals of Amazonian forest fragments: pattern and process. PhD Dissertation, University of Florida.

    Google Scholar 

  • Marquis, R.J.: 1984. Leaf herbivores decrease fitness of a tropical plant. Science 226, 537–539.

    Article  CAS  Google Scholar 

  • Marquis, R.J.: 1991. Herbivore fauna of Piper (Piperaceae) in a Costa Rican wet forest: diversity, specificity and impact, pp 179–208. in Price, P.W., Lewinsohn, M, Fernandes, G.W. and Benson, W.W. Plant-Animal Interactions: Evolutionary Ecology in Tropical and Temperate Regions, Wiley, NY.

    Google Scholar 

  • Marquis, R.J. and Braker, H.E.: 1993. Plant/herbivore interactions at La Selva: Diversity, specialization and impact on plant populations, pp 263–281 in McDade, L., Hartshorn, G.H., Hespenheide, H. and Bawa, K. La Selva: Ecology and Natural History of a Neotropical Rainforest, University of Chicago Press, Chicago.

    Google Scholar 

  • Mattson, W.J. and Addy, N.D.: 1975. Phytophagous insects as regulators of forest primary production. Science 190, 515–522.

    Article  Google Scholar 

  • Mattson, W.J. and Haack, R.A.: 1987, The role of drought stress in provoking outbreaks of phytophagous insects, pp 365–410 in Barbosa, P. and Schultz, J.C. (eds) Insect Outbreaks, Academic Press, San Diego.

    Google Scholar 

  • Mooney, H.A., Medina, E., Schindler, D.W., Schulze, E.-D. and Walker, B.H. (eds) 1991. Ecosystem Experiments. John Wiley and Sons, NY.

    Google Scholar 

  • Nascimento, M.T. and Proctor, J.: 1994. Insect defoliation of a monodominant Amazonian rainforest. J Trop Ecol 10, 633–636.

    Article  Google Scholar 

  • Norby, R.J., O’Neill, E.G. and Luxmoore, R.J.: 1986. Effects of atmospheric C02 enrichment on the growth and mineral nutrition of Quercus alba seedlings in nutrient-poor soil. Plant Physiol 82, 83–89.

    Article  CAS  Google Scholar 

  • Oberbauer, S.O., Sionit, N. Hastings, S.J. and Oechel, W.C.: 1986. Effects of carbon dioxide enrichment on growth, photosynthesis, and nutrient concentration of Alaskan tundra plant species. Can J Bot 64, 2993–2998.

    Article  CAS  Google Scholar 

  • Osbrink, W.L.A., Trumble, J.T. and Wagner, R.E.: 1987. Host suitability of Phaseolus lunata for Trichoplusia ni (Lepidoptera: Noctuidae) in controlled carbon dioxide atmospheres. Environ Entomol 16, 210–215.

    Google Scholar 

  • Patino, S., Herre, E.A. and Tyree, M.T.: 1994. Physiological determinants of Ficus fruit temperature and implications for survival of pollinator wasp species: comparative physiology through an energy budget approach. Oecologia 100, 13–20.

    Article  Google Scholar 

  • Price, P.W.: 1987, the role of natural enemies in insect populations, pp 287–313 in Barbosa, P. and Schultz, J.C. (eds) Insect Outbreaks, Academic Press, San Diego.

    Google Scholar 

  • Price, P.W.: 1989. Clonal development of coyote willow, Salix exigua (Salicaceae) and attack by the shoot-galling sawfly, Euura exigua (Hymenoptera: Tenthredinidae). Environ Ent 18, 61–68.

    Google Scholar 

  • Price, P.W, Bouton, C.E., Gross, P., McPherson, B.A., Thompson, J.N. and Weis, A.E.: 1980. Interactions among three trophic levels: Influence of plants on interactions between insect herbivores and natural enemies. Ann Rev Ecol & Syst 11, 41–65.

    Article  Google Scholar 

  • Quinn, W.H. and Neal, V.T.: 1992. The historical record of El Nino events, pp 623–648 in: Bradley, R.S. and Jones, P.D. (eds) Climate Since A.D. 1500, Routledge, London.

    Google Scholar 

  • Reekie, E.G. and Bazzaz, F.A.: 1989. Competition and patterns of resource use among seedlings of five tropical trees grown at ambient and elevated C02. Oecologia 7, 9212–222.

    Google Scholar 

  • Reichle, D.E., Goldstein, R.A., Van Hook, R.I., Jr., and Dodson, G.J.: 1973. Analysis of insect consumption in a forest canopy. Ecology 54, 1076–1084.

    Article  Google Scholar 

  • Reid, C.D. and Strain, B.R.: 1994. Effects of C02 enrichment on whole-plant carbon budget of seedlings of Fagus grandifolia and Acer saccharum in low irradiance. Oecologia 98, 31–39.

    Article  Google Scholar 

  • Rhoades, D.F.: 1979. Evolution of plant chemical defense against herbivores, pp 3–54 in Rosenthal, G.A. and Janzen, D.H. (eds) Herbivores: Their Interaction with Secondary Plant Metabolites, Acad Press, NY.

    Google Scholar 

  • Roth, S.K. and Lindroth, R.L.: 1994. Effects of C02-mediated changes in paper birch and white pine chemistry on gypsy moth performance. Oecologia 98, 133–138.

    Article  Google Scholar 

  • Roth, S.K., Lindroth, R.L. and Montgomery, M.E.: 1994, Effects of foliar phenolics and ascorbic acid on performance of the gypsy moth (Lymantria dispar). BiochemSyst & EcolU, 341–351.

    Google Scholar 

  • Roth, S.K. and Lindroth, R.L.: 1995. Elevated atmospheric C02: effects on phytochemistry, insect performance and insect-parasitoid interactions. Global Change Biol 1, 173–182.

    Article  Google Scholar 

  • Stamp, N.E. and Yang, Y.: 1996, Response of insect herbivires to multiple allelochemicals under different thermal regimes, Ecology 77, 1088–1102.

    Article  Google Scholar 

  • Strain, B.R. and Bazzaz, F.A.: 1983. Terrestrial plant communities, in C0 2 and Plants: The Response of Plants to Rising Levels of Atmospheric Carbon Dioxide, AAAS Selected Symposium 84. Westview Press, Boulder.

    Google Scholar 

  • Strain, B.R and Cure, J.D.: 1985. Direct effects of increasing carbon dioxide on vegetation (DOE/ER-0238). U.S. Dept Energy, Washington D.C.

    Google Scholar 

  • Strong D.R., Lawton, J.H., and Southwood T.R.E.: 1984. Insects on Plants: Community Patterns and Mechanisms. Blackwell Scientific, Oxford, GB

    Google Scholar 

  • Terborgh, J.: 1983. Five New World Primates. Princeton University Press, Princeton.

    Google Scholar 

  • Terborgh, J.: 1986. Keystone plant resources in the tropical forest, pp 330–344 in Soule, M.E. (ed). Conservation Biology: The Science of Scarcity and Diversity. Sinauer, Sunderland, MA.

    Google Scholar 

  • Tobin, M.F., Lopez, O.R. and Kursar, T.A.: 1997, Drought response of tropical understory species with long and short leaf lifespans, (submitted to Biotropica).

    Google Scholar 

  • White, T.C.R.: 1974. A hypothesis to explain outbreaks of looper caterpillars with special reference to populations of Selidosema suavis in a plantation of Pinus radiata in New Zealand. Oecologia 16, 279–301.

    Article  Google Scholar 

  • White, T.C.R.: 1976. Weather, food and plagues of locusts. Oecologia 22, 119–134.

    Article  Google Scholar 

  • Williams, E.E., Garbutt, K. Bazzaz, F.A. and Vitousek, P.M.: 1986. The response of plants to elevated C02. IV. Two deciduous-forest tree communities. Oecologia 69, 454–459.

    Article  Google Scholar 

  • Williams, R.S., Lincoln, D.E. and Thomas, R.B.: 1994. Loblolly pine grown under elevated C02 affects early instar pine sawfly performance. Oecologia 98, 64–71.

    Article  Google Scholar 

  • Windsor, D.M.: 1990. Climate and moisture variability in a tropical forest, long-term records for Barro Colorado Island, Panama. Smithsonian Contributions to Earth Sciences 29, 1–145.

    Article  Google Scholar 

  • Winter, K. and Virgo, A.: 1997. Elevated C02 enhances growth in the rainforest understory plant, Piper cordulatum, at extremely low light intensities. Flora, (in press).

    Google Scholar 

  • Wolda, H.: 1978. Fluctuations in abundance of tropical insects. Amer Nat 112, 1017–1045.

    Article  Google Scholar 

  • Wolda, H. and Foster, R.: 1978. Zunacetha annulata (Lepidoptera: Dioptidae), an outbreak insect in a neotropical forest. Geo-Eco-Trop 2, 443–454.

    Google Scholar 

  • Wong, M., Wright, S.J., Hubbell, S.P., and Foster, R.B.: 1990. The spatial pattern and reproductive consequences of outbreak defoliation in Quararibea asterolepis, a tropical tree. J. Ecology 78, 579–588.

    Article  Google Scholar 

  • Wong, S.C.: 1979. Elevated atmospheric partial pressure of C02 and plant growth. Oecologia 44, 68–74.

    Article  Google Scholar 

  • Yang, Y. and Stamp, N.E.: 1995, Simultaneous effects of night-time temperature and an allelochemical on performance of an insect herbivore, Oecologia 104, 225–233.

    Article  Google Scholar 

  • Yang, Y. and Stamp, N.E.: 1996, Effects of temperature, multiple allelochemicals and larval age on the performance of a specialist caterpillar, Entomol Exp Appl 79, 335–344.

    Article  Google Scholar 

  • Ziska, L.H., Hogan, K.P., Smith, A.P. and Drake, B.G.: 1991. Growth and photosynthetic response of nine tropical species with long-term exposure to elevated carbon dioxide. Oecologia 86, 383–389.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1998 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Coley, P.D. (1998). Possible Effects of Climate Change on Plant/Herbivore Interactions in Moist Tropical Forests. In: Markham, A. (eds) Potential Impacts of Climate Change on Tropical Forest Ecosystems. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-2730-3_15

Download citation

  • DOI: https://doi.org/10.1007/978-94-017-2730-3_15

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-90-481-5046-5

  • Online ISBN: 978-94-017-2730-3

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics