Skip to main content

Do Frugivore Population Fluctuations Reflect Fruit Production? Evidence from Panama

  • Chapter
Tropical Fruits and Frugivores

Abstract

To conserve tropical mammals, it is important to understand factors affecting the range of population fluctuations that normally occur over both the short and long term. Annual shifts in the population size of many species may be tied, at least in part, to phenological production patterns of plants, which in turn are often affected by climatic events. To examine the influence of annual fruit crop size on population dynamics of frugivorous mammals, we compared estimates of fruit production and the relative abundance of four frugivorous mammal species (agoutis, squirrels, capuchin monkeys, howler monkeys) for 15 years on Barro Colorado Island, Republic of Panama. Species differed in the magnitude of population fluctuation. Howler monkey population estimates showed little annual fluctuation and no significant relationship to fruit production. In contrast, population estimates for agoutis, squirrels and capuchin monkeys showed interannual fluctuations, at times dramatic, but these were not always concordant nor did they necessarily appear to relate to fruit production estimates, either within years or with a one-or two-year lag. Fruit production data suggest that, on average, in any given year only 20 to 30% of the mid-to-late rainy season species producing fruits important to frugivores will have an unusually good year; other species will have an average to sub-standard year. The next year, 20 to 30% of the other important fruit species in this temporal cohort will have an unusually good year—though one cannot predict in advance which species they will be. This oscillating production pattern makes it difficult to predict, except in extreme years, how the frugivore community or individual species will be affected by fruit availability. To draw conclusions on this topic, more detailed data are required on annual fruit production patterns of a representative sample of individuals of important fruit species as well as data on reproductive and other relevant traits of each mammal species. The possibility remains that many mammal populations may be affected more immediately by top-down factors such as predators, parasites or disease rather than by bottom-up factors such as fruit availability. As population parameters for each mammal species are likely influenced by a continuously varying combination of factors, barring effects of rare environmental events, f the particular set of factors affecting the population dynamics of one frugivorous species in any given year may not necessarily impact similarly in that year on other frugivorous species at that same site.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
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

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Alvin, P. de T. (1960). Moisture stress as a requirement for the flowering of coffee. Science, 132, 354.

    Google Scholar 

  • Andresen, E. (1999). Seed dispersal by monkeys and the fate of dispersed seeds in a Peruvian rain forest. Biotropica, 31, 145–158.

    Google Scholar 

  • Ashton, P. S., Givnich, T. J. & Appanah, S. (1988). Staggered flowering in the Dipterocarpaceae: new insights into floral induction and the evolution of mast fruiting in the aseasonal tropics. American Naturalist, 132, 44–66.

    Article  Google Scholar 

  • Asquith, N. M., Wright, S. J. & Clauss, J. M. (1997). Does mammal community composition control recruitment in Neotropical forests? Evidence from Panama. Ecology, 78, 941–946.

    Google Scholar 

  • Asquith, N. M., Terborgh, J., Arnold, A. E., & Riveros, C. M. (1999). The fruits the agouti ate: Hymenaea courbaril seed fate when its disperser is absent. Journal of Tropical Ecology, 15, 299–235.

    Article  Google Scholar 

  • Bodmer, R. E. (1990). Responses of ungulates to seasonal inundations in the Amazonian floodplain. Journal of Tropical Ecology, 6, 191–201.

    Google Scholar 

  • Corlett, R. T. (2002). Frugivory and seed dispersal in degraded tropical East Asian landscapes. In D.J. Levey, W. R. Silva & M. Galetti (Eds.), Seed dispersal and frugivory: Ecology, evolution and conservation (pp. 451–466). Oxford: CABI Publishing.

    Google Scholar 

  • Conklin-Brittain N. L., Wrangham, R. W., & Hunt, K. D. (1998). Dietary response of chimpanzees and Cercopithecines to seasonal variation in fruit abundance. II. Macronutrients. International Journal of Primatology, 19, 971–997.

    Article  Google Scholar 

  • Den Boer P. J. & Reddingius,. J. (1996). Regulation and stabilization paradigms in population ecology. London: Chapman and Hall.

    Google Scholar 

  • Dirzo, R. & Miranda, A. (1991). Altered patterns of herbivory and diversity in the forest understory: a case study of the possible consequences of contemporary defaunation. In P. W. Price, T. M. Lewinsohn, G. W. Fernandes & W. W. Benson (Eds.), Plant-animal interactions: Evolutionary ecology in tropical and temperate regions (pp. 273–287). New York: John Wiley and Sons.

    Google Scholar 

  • Foster, M. S. & Terborgh, J. (1998). Impact of a rare storm event on an Amazonian forest. Biotropica, 30(3), 470–474.

    Google Scholar 

  • Foster, R. B. (1982a). Famine on Barro Colorado Island. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 201–212). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Foster, R. B. (1982b). The seasonal rhythm of fruit fall on Barro Colorado Island. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 151–172). Washington, D.C.: Smithsonian Press.

    Google Scholar 

  • Foster, R. B. &. Brokaw, N. V. L. (1982). Structure and history of the vegetation of Barro Colorado Island. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 67–82). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Fragoso, J. M. (1998). Home range and movement patterns of white-lipped peccary (Tayassu pecari) herds in the northern Brazilian Amazon. Biotropica, 30(3), 458–469.

    Google Scholar 

  • Furuichi, T., Hashimoto, C. &. Tashiro, Y. (2001). Fruit availability and habitat use by chimpanzees in the Kalinzu Forest, Uganda: Examination of fallback foods. International Journal of Primatology, 22, 929–945.

    Google Scholar 

  • Gautier-Hion, A. & Michaloud, G. (1989). Are figs always keystone resources for tropical frugivorous vertebrates? A test in Gabon. Ecology, 70, 1826–1833.

    Google Scholar 

  • Getz, W. M. (1996). A hypothesis regarding the abruptness of density dependence and the growth rate of populations. Ecology, 77, 2014–2026.

    Google Scholar 

  • Giacalone-Madden, J., Glanz, W. E., & Leigh, E. G. (1990). Fluctuaciones poblacionales a largo plazo de Sciurus granatensis en relacion con la disponibilidad de frutos. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecologia de un bosque tropical (pp. 331–336). Washington D.C: Smithsonian Press.

    Google Scholar 

  • Glanz, W. E., Thorington, R., Giacalone-Madden, J. &. Heaney, L. R. (1982). Seasonal food use and demographic trends in Sciurus granatensis. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 239–252). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Glanz, W. E. (1982). The terrestrial mammal fauna of Barro Colorado Island: censuses and long-term changes. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 455–468). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Gilbert, L. E. (1980). Food web organization and conservation of Neotropical biodiversity. In M. E. Soulé & B. A. Wilcox (Eds.). Conservation Biology (pp 11–34). Sunderland, MA: Sinauer.

    Google Scholar 

  • Gompper, M. E. (1996). Population ecology of the white-nosed coati (Nasua narica) on Barro Colorado Island, Panama. Journal of Zoology, 241, 441–455.

    Google Scholar 

  • Harms, K. E., Wright, S. J., Calderón, O., Hernandéz, A. &. Herre, E. A. (2000). Pervasive density-dependent recruitment enhances seedling diversity in a tropical forest. Nature, 404, 493–495.

    Article  PubMed  CAS  Google Scholar 

  • Herre, A. (1993). Population structure and the evolution of virulence in nematode parasites of fig wasps. Science, 259, 1442–1445.

    PubMed  Google Scholar 

  • Hubbell, S. P., Foster, R. B., O’Brien, S. T., Harms, K. E., Condit, R., Weschler, B., Wright, S. J., & Loo de Lao, S. (1999). Light gap disturbances, recruitment limitation, and tree diversity in a neotropical forest. Science, 283, 554–557.

    Article  PubMed  CAS  Google Scholar 

  • Jordano, P. & Godoy, J. A. (2002) Frugivore-generated seed shadows: A landscape view of demographic and genetic effects. In D.J. Levey, W.R. Silva & M. Galetti (Eds.), Seed dispersal and frugivory: Ecology, evolution and conservation (pp. 305–322). Oxford: CABI Publishing.

    Google Scholar 

  • Karr, J. R. & Freemark, K. E. (1983). Habitat selection and environmental gradients: dynamics in the “stable” tropics. Ecology, 64, 1481–1494.

    Google Scholar 

  • Leigh, E. G. (1999). Tropical forest ecology. New York: Oxford University Press.

    Google Scholar 

  • Leigh, E. G. & Smythe, N. (1978). Leaf production, leaf consumption, and the regulation of folivory on Barro Colorado Island, In G.G. Montgomery (Ed.), The ecology of arboreal folivores (pp. 33–50). Washington, D. C: Smithsonian Press.

    Google Scholar 

  • Leigh, E. G., Rand, A. S., & Windsor, D. M. (Eds.) (1982). Ecology of a tropical forest. Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Leith, H. & Whittaker, R. H. (1975). Primary productivity of the biosphere. Series Ecological Studies 14. New York: Springer-Verlag.

    Google Scholar 

  • Matthews, J. D. (1963). Factors affecting the production of seed by forest trees. Forestry Abstracts, 24, 1–13.

    Google Scholar 

  • Milton, K. (1980). The foraging strategy of howler monkeys: A study in primate economics. New York: Columbia University Press.

    Google Scholar 

  • Milton, K. (1982). The role of resource seasonality in density regulation of a wild primate population. In E.G. Leigh, A.S. Rand & D.M. Windsor (Eds.), Ecology of a tropical forest (pp. 273–289). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Milton, K. (1990). Annual mortality patterns of a mammal community in central Panama. Journal of Tropical Ecology, 6, 493–499.

    Google Scholar 

  • Milton, K. (1991). Annual patterns of leaf and fruit production by six Neotropical Moraceae species. Journal of Ecology, 79, 1–26.

    Google Scholar 

  • Milton, K. (1996). Interactions between a host-specific bot fly, Alouattamyia baeri, and a free-ranging howler monkey (Alouatta palliata) population in Panama. Journal of Zoology, 239, 39–63.

    Article  Google Scholar 

  • Oppenheimer, J.R. (1982). Cebus capucinus: home range, population dynamics and interspecific relationships. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 253–272). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Peres, C. A. (1994). Composition, density and fruiting phenology of arborescent palms in an Amazonian terre firme forest. Biotropica, 26, 285–294..

    Google Scholar 

  • Rand, A. S. & Windsor, D. M. (1982). Variation in rainfall on Barro Colorado Island, Panama. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 47–59). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Rowell, T. E. & Mitchell, B. (1991). Comparison of seed dispersal by guenons in Kenya and capuchins in Panama. Journal of Tropical Ecology, 7, 269–274.

    Article  Google Scholar 

  • Schaefer, H. M. & Schmidt, V. (2002). Vertical stratification and caloric content of the standing fruit crop in a tropical lowland forest. Biotropica, 34, 244–253.

    Google Scholar 

  • Smythe, N., Glanz, W. E. & Leigh, E. G. (1982). Population regulation in some terrestrial frugivores. In E. G. Leigh, A. S. Rand & D. M. Windsor (Eds.), Ecology of a tropical forest (pp. 227–238). Washington, D.C: Smithsonian Press.

    Google Scholar 

  • Swaine, M. D., Lieberman, D., & Putz, F. E. (1987). The dynamics of tree populations in a tropical forest. Journal of Tropical Ecology, 3, 359–367.

    Google Scholar 

  • Terborgh, J. (1983). Five new world primates: A study in comparative ecology. Princeton: Princeton University Press.

    Google Scholar 

  • Terborgh, J. (1986). Keystone plant resources in a tropical forest. In M.E. Soule, (Ed.) Conservation Biology (pp. 330–344). New York: Academic Press.

    Google Scholar 

  • Van Schaik, C. P., Terborgh, J. & Wright, S. J. (1993). The phenology of tropical forests: adaptive significance and the consequences for primary consumers. Annual Review of Ecological Systems, 24, 353–377.

    Google Scholar 

  • Whitmore, T. C. (1991). Tropical rain forest dynamics and its implications for management. In A. Gomes-Pampa, T.C. Whitmore, & M. Hadley (Eds.) Rainforest regeneration and management (pp. 67–89). Paris, France: UNESCO.

    Google Scholar 

  • Wikelski, M., Hau, M., & Wingfield, J. C. (2000). Seasonality of reproduction in a Neotropical rain forest bird. Ecology, 81, 2458–2472.

    Google Scholar 

  • Wolda, H. (1983). “Long-term” stability of tropical insect populations. Research in Population Ecology Supplement, 3, 112–126.

    Google Scholar 

  • Wright, S. J. & Calderon, O. (1995). Phylogenic constraints on tropical flowering phenologies. Journal of Ecology, 83, 937–948.

    Google Scholar 

  • Wright, S. J., Carrasco, C., & Calderon, O. (1996). Community-level fruit failure and famine among mammalian frugivores in a tropical rain forest. Bulletin of the Ecological Society of America, 77,supplement:492.

    Google Scholar 

  • Wright, S. J., Carrasco, C., Calderon, O., & Paton, S. (1999). The El Niño southern oscillation, variable fruit production, and famine in a tropical forest. Ecology, 80(5), 1632–1647.

    Google Scholar 

  • Wright, S. J. & Duber. H. C. (2001). Poachers and forest fragmentation alter seed dispersal, seed survival, and seedling recruitment in the palm Attalea butyraceae, with implications for tropical tree diversity. Biotropica, 33, 583–595.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2005 Springer

About this chapter

Cite this chapter

Milton, K., Giacalone, J., Wright, S.J., Stockmayer, G. (2005). Do Frugivore Population Fluctuations Reflect Fruit Production? Evidence from Panama. In: Dew, J.L., Boubli, J.P. (eds) Tropical Fruits and Frugivores. Springer, Dordrecht. https://doi.org/10.1007/1-4020-3833-X_2

Download citation

Publish with us

Policies and ethics