International Journal of Primatology

, Volume 29, Issue 2, pp 379–403 | Cite as

Diet and Feeding Ecology of Ateles chamek in a Bolivian Semihumid Forest: The Importance of Ficus as a Staple Food Resource

  • Annika M. Felton
  • Adam Felton
  • Jeff T. Wood
  • David B. Lindenmayer
Article

Abstract

We describe temporal patterns of food consumption by Peruvian spider monkeys (Ateles chamek) in a semihumid forest in lowland Bolivia. We assessed dietary composition in relation to temporal variation in abundance, duration, and synchrony of different food items in their home range. We collected data from September 2003 to September 2004, in the forestry concession La Chonta, Department of Santa Cruz. Throughout the period of detailed feeding data collection (February-September 2004), Ateles chamek used Ficus as a staple food resource. Figs constituted almost 50% of their diet in terms of total time spent feeding, and subjects consumed them to a great extent even during times of high overall food availability. This is contrary to the general expectation that for Neotropical frugivores, Ficus is a fallback food in times of fruit scarcity, rather than a staple food resource. Surprisingly, despite being considered ripe fruit specialists, Ateles chamek spent 18% of their feeding times eating unripe figs. Ateles chamek consumed unripe figs all through the year, including periods when ripe figs and other ripe fruit were abundant. We identify other important fallback foods for Ateles chamek in the forest, in particular the ripe fruit of Myrciaria sp.

Keywords

Ateles chamek diet Ficus boliviana fig unripe fruit 

References

  1. Akaike, H. (1974). A new look at statistical model identification. IEEE Transactions on Automatic Control, 19, 716–722.CrossRefGoogle Scholar
  2. August, P. V. (1981). Fig fruit consumption and seed dispersal by Artibeus jamaicensis in the Llanos of Venezuela. Biotropica, 13, 70–76.CrossRefGoogle Scholar
  3. Bawa, K. S., & Krugman, S. L. (1991). Reproductive biology and genetics of tropical trees. In A. Gomez-Pompa, T. C. Whitmore, & M. Hadley (Eds.) Rain Forest Regeneration and Management. Paris: UNESCO and The Parthenon Publishing Group.Google Scholar
  4. Bawa, K. S., Perry, D. R., & Beach, J. H. (1985). Reproductive biology of tropical lowland rain-forest trees.1. Sexual systems and incompatibility mechanisms. American Journal of Botany, 72, 331–345.CrossRefGoogle Scholar
  5. Cant, J. G. H. (1990). Feeding ecology of spider monkeys (Ateles geoffroyi) at Tikal, Guatemala. Human Evolution, 5, 269–281.CrossRefGoogle Scholar
  6. Castellanos, H. G. (1995). Feeding Behaviour of Ateles belzebuth E. Geoffroy 1806 (Cebidae: Atelinae) in Tawadu Forest Southern Venezuela. Ph.D Dissertation (unpublished), The University of Exeter, U.K.Google Scholar
  7. Chapman, C. (1987). Flexibility in diets of three species of Costa Rican primates. Folia Primatologica, 49, 90–105.CrossRefGoogle Scholar
  8. Chapman, C. (1988). Patterns of foraging and range use by three species of Neotropical primates. Primates, 29, 177–194.CrossRefGoogle Scholar
  9. Chapman, C. A., & Chapman, L. J. (1990). Dietary variability in primate populations. Primates, 31, 121–128.CrossRefGoogle Scholar
  10. Chapman, C. A., Wrangham, R., & Chapman, L. J. (1994). Indexes of habitat-wide fruit abundance in tropical forests. Biotropica, 26, 160–171.CrossRefGoogle Scholar
  11. Conklin, N. L., & Wrangham, R. W. (1994). The value of figs to a hind-gut fermenting frugivore - a nutritional analysis. Biochemical Systematics and Ecology, 22, 137–151.CrossRefGoogle Scholar
  12. Dew, J. L. (2001). Synecology and Seed Dispersal in Woolly Monkeys (Lagothrix lagotricha poeppigii) and Spider Monkeys (Ateles belzebuth belzebuth) in Parque Nacional Yasuni, Ecuador. PhD dissertation, University of California Davis.Google Scholar
  13. Dew, J. L. (2005). Foraging, food choice, and food processing by sympatric ripe-fruit specialists: Lagothrix lagotricha poeppigii and Ateles belzebuth belzebuth. International Journal of Primatology, 26, 1107–1135.CrossRefGoogle Scholar
  14. Di Fiore, A., & Campbell, C. J. (2007). The Atelines: Variation in ecology, behavior, and social organization. In C. J. Campbell, A. Fuentes, K. C. MacKinnon, M. Panger, & S. K. Bearder (Eds.) Primates in Perspective (pp. 155–185). Oxford: Oxford University Press.Google Scholar
  15. Di Fiore, A., Link, A., & Dew, J. L. (in press). Diets of wild spider monkeys. In C. J. Campbell (Ed.) Spider Monkeys: Behavior, Ecology and Evolution of the Genus Ateles. Cambridge, U.K.: Cambridge University Press.Google Scholar
  16. Fredericksen, T. S., Rumiz, D., Bravo, M. J. J., & Abacay, R. A. (1999). Harvesting free-standing fig trees for timber in Bolivia: Potential implications for forest management. Forest Ecology and Management, 116, 151–161.CrossRefGoogle Scholar
  17. Iwanaga, S., & Ferrari, S. F. (2001). Party size and diet of syntopic atelids (Ateles chamek and Lagothrix cana) in southwestern Brazilian Amazonia. Folia Primatologica, 72, 217–227.CrossRefGoogle Scholar
  18. Janson, C. H., & Chapman, C. A. (1999). Resources and primate community structure. In J. G. Fleagle, C. Janson, & K. E. Reed (Eds.) Primate Communities (pp. 237–267). Cambridge, U.K.: Cambridge University Press.Google Scholar
  19. Janzen, D. H. (1979). How to be a fig. Annual Review of Ecology and Systematics, 10, 13–51.CrossRefGoogle Scholar
  20. Janzen, D. H., ed. (1983). Costa Rican Natural Histrory. Chicago: University of Chicago Press.Google Scholar
  21. Justiniano, M. J., & Fredericksen, T. S. (2000). Phenology of tree species in Bolivian dry forests. Biotropica, 32, 276–281.Google Scholar
  22. Justiniano, M. J., Peña-Claros, M., Gutiérrez, M., Toledo, M., Jordán, C., Vargas, I., & Montero, J. C. (2003). Guía dendrológica de espécies forestales de Bolívia-Volumen II. Proyecto BOLFOR, Santa Cruz, Bolívia.Google Scholar
  23. Kinzey, W. G. (1997). Ateles. In W. G. Kinzey (Ed.) New World Primates: Ecology, Evolution, and Behavior (pp. 192–199). New York: Aldine de Gruyter.Google Scholar
  24. Klein, L. L., & Klein, D. B. (1977). Feeding behaviour of the Colombian spider monkey. In T. H. Clutton-Brock (Ed.) Primate Ecology: Studies of Feeding and Ranging Behaviour in Lemurs, Monkeys and Apes (pp. 153–181). New York: Academic Press.Google Scholar
  25. Krebs, C. (1989). Ecological Methodology. (ed.), Harper & Row, New York.Google Scholar
  26. Kubitzki, K., & Kurz, H. (1984). Synchronized dichogamy and dioecy in Neotropical Lauraceae. Plant Systematics and Evolution, 147, 253–266.CrossRefGoogle Scholar
  27. Leighton, M., & Leighton, D. R. (1982). The relationship of size of feeding aggregate to size of food patch: Howler monkeys (Alouatta palliata) feeding in Trichilia cipo fruit trees on Barro Colorado Island. Biotropica, 14, 81–90.CrossRefGoogle Scholar
  28. Leighton, M., & Leighton, D. R. (1983). Vertebrate responses to fruiting seasonality within a Bornean rain forest. In S. L. Sutton, T. C. Whitmore, & A. C. Chadwick (Eds.) Tropical Rain Forest: Ecology and Management (pp. 181–196). Oxford: Blackwell.Google Scholar
  29. McDiarmid, R. W., Ricklefs, R. E., & Foster, M. S. (1977). Dispersal of Stemmadenia donnell-smithii (Apocynaceae) by birds. Biotropica, 9, 9–25.CrossRefGoogle Scholar
  30. Milton, K. (1980). The Foraging Strategy of Howler Monkeys: A Study in Primate Economics. (ed.), New York: Columbia University Press.Google Scholar
  31. Milton, K. (1991). Leaf change and fruit production in 6 Neotropical Moraceae species. Journal of Ecology, 79, 1–26.CrossRefGoogle Scholar
  32. Milton, K. (1993). Diet and primate evolution. Scientific American Aug:86–93.Google Scholar
  33. Milton, K., Windsor, D. M., Morrison, D. W., & Estribi, M. A. (1982). Fruiting phenologies of two Neotropical Ficus species. Ecology, 63, 752–762.CrossRefGoogle Scholar
  34. Mostacedo, B., & Fredericksen, T. S. (1999). Regeneration status of important tropical forest tree species in Bolivia: Assessment and recommendations. Forest Ecology and Management, 124, 263–273.CrossRefGoogle Scholar
  35. Mostacedo, B., Justiniano, M. J., Toledo, M., & Fredericksen, T. S. (2003). Guía dendrológica de espécies forestales de Bolívia-Volumen I. Proyecto BOLFOR, Santa Cruz, Bolívia.Google Scholar
  36. Newton-Fisher, N. E. (1999). The diet of chimpanzees in the Budongo Forest Reserve, Uganda. African Journal of Ecology, 37, 344–354.CrossRefGoogle Scholar
  37. Norconk, M. A., Grafton, B. W., & Conklin-Brittain, N. L. (1998). Seed dispersal by Neotropical seed predators. American Journal of Primatology, 45, 103–126.PubMedCrossRefGoogle Scholar
  38. Nunes, A. (1998). Diet and feeding ecology of Ateles belzebuth belzebuth at Maraca Ecological Station, Roraima, Brazil. Folia Primatologica, 69, 61–76.CrossRefGoogle Scholar
  39. O’Brien, T. G., Kinnaird, M., & Dierenfeld, E. S. (1998). What’s so special about figs? Nature, 392, 668.CrossRefGoogle Scholar
  40. Park, A., Justiniano, M. J., & Fredericksen, T. S. (2005). Natural regeneration and environmental relationships of tree species in logging gaps in a Bolivian tropical forest. Forest Ecology and Management, 217, 147–157.CrossRefGoogle Scholar
  41. Peters, R. H., Cloutier, S., Dubé, D., Hastings, P., Kaiser, H., Kohn, D., et al. (1988). The allometry of the weight of fruit on trees and shrubs in Barbados. Oecologia, 74, 612–616.CrossRefGoogle Scholar
  42. Ressell, K., Guilherme, F. A. G., Schiavini, I., & Oliveira, P. E. (2004). Ecologia morfofuncional de plântulas de espécies arbóreas da Estação Ecológica do Panga, Uberlândia, Minas Gerais. Revista Brasiliera Botânica, 27, 311–323.Google Scholar
  43. Russo, S. E., Campbell, C. J., Dew, J. L., Stevenson, P. R., & Suarez, S. A. (2005). A multi-forest comparison of dietary preferences and seed dispersal by Ateles spp. International Journal of Primatology, 26, 1017–1037.CrossRefGoogle Scholar
  44. Schatz, G. E., Williamson, G. B., Cogswell, C. M., & Stam, A. C. (1985). Stilt roots and growth of arboreal palms. Biotropica, 17, 206–209.CrossRefGoogle Scholar
  45. Serio-Silva, J. C., Rico-Gray, V., Hernandez-Salazar, L. T., & Espinosa-Gomez, R. (2002). The role of Ficus (Moraceae) in the diet and nutrition of a troop of Mexican howler monkeys, Alouatta palliata mexicana, released on an island in southern Veracruz, Mexico. Journal of Tropical Ecology, 18, 913–928.CrossRefGoogle Scholar
  46. Shanahan, M., So, S., Compton, S. G., & Corlett, R. (2001). Fig-eating by vertebrate frugivores: A global review. Biological Reviews, 76, 529–572.PubMedGoogle Scholar
  47. Stevenson, P. R., Quinones, M. J., & Ahumada, J. A. (2000). Influence of fruit availability on ecological overlap among four Neotropical primates at Tinigua National Park, Colombia. Biotropica, 32, 533–544.Google Scholar
  48. Suarez, S. A. (2006). Diet and travel costs for spider monkeys in a nonseasonal, hyperdiverse environment. International Journal of Primatology, 27, 411–436.CrossRefGoogle Scholar
  49. Symington, M. M. (1988). Food competition and foraging party size in the black spider monkey (Ateles paniscus chamek). Behaviour, 105, 117–134.CrossRefGoogle Scholar
  50. Terborgh, J. (1983). Five New World Monkeys. (ed.), Princeton University Press, Princeton, New Jersey.Google Scholar
  51. Terborgh, J. (1986). Keystone plant resources in the tropical forest. In M. E. Soulé (Ed.) Conservation Biology (pp. 330–344). New York: Academic Press.Google Scholar
  52. van Roosmalen, M. G. M. (1985). Habitat preferences, diet, feeding behavior and social organization of the black spider monkey, Ateles paniscus paniscus, in Surinam. ACTA Amazonica, 15(Suppl), 1–231.Google Scholar
  53. van Schaik, C. P., Terborgh, J. W., & Wright, S. J. (1993). The phenology of tropical forests - Adaptive significance and consequences for primary consumers. Annual Review of Ecology and Systematics, 24, 353–377.Google Scholar
  54. Wallace, R. B. (1998). The Behavioural Ecology of Black Spider Monkeys in North-eastern Bolivia. PhD Dissertation, University of Liverpool.Google Scholar
  55. Wallace, R. B. (2005). Seasonal variations in diet and foraging behavior of Ateles chamek in a southern Amazonian tropical forest. International Journal of Primatology, 26, 1053–1075.CrossRefGoogle Scholar
  56. Wallace, R. B. (2006). Seasonal variations in black-faced black spider monkey (Ateles chamek) habitat use and ranging behavior in a southern Amazonian tropical forest. American Journal of Primatology, 68, 313–332.PubMedCrossRefGoogle Scholar
  57. Wallace, R. B., Painter, R. L. E., Rumiz, D., & Taber, A. (2000). Primate diversity, distribution and relative abundances in the Rio Blanco y Rio Negro Wildlife Reserve, Santa Cruz Department, Bolivia. Neotropical Primates, 8, 24–28.Google Scholar
  58. White, F. J. (1998). Seasonality and socioecology: The importance of variation in fruit abundance to bonobo sociality. International Journal of Primatology, 19, 1013–1027.CrossRefGoogle Scholar
  59. Wrangham, R. W., Conklin, N. L., Etot, G., Obua, J., Hunt, K. D., Hauser, M. D., et al. (1993). The value of figs to chimpanzees. International Journal of Primatology, 14, 243–256.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2008

Authors and Affiliations

  • Annika M. Felton
    • 1
    • 2
  • Adam Felton
    • 1
    • 2
  • Jeff T. Wood
    • 1
  • David B. Lindenmayer
    • 1
  1. 1.Fenner School of Environment and SocietyAustralian National UniversityCanberraAustralia
  2. 2.Institituto Boliviano de Investigación Forestal (IBIF)Santa Cruz de la SierraBolivia

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