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Rain-forest canopy-connectivity and habitat selection by a small neotropical primate, Geoffroy's tamarin (Saguinus geoffroyi)

Published online by Cambridge University Press:  11 October 2010

D. Madden*
Affiliation:
Smithsonian Tropical Research Institute, 1100 Jefferson Drive, Washington DC, 20560, USA
P. A. Garber
Affiliation:
Department of Anthropology, Program in Ecology, Evolution, and Conservation Biology, University of Illinois, Urbana, IL 61801, USA
S. L. Madden
Affiliation:
MJC Biology Department, 435 College Ave, Modesto, CA. 95350, USA
C. A. Snyder
Affiliation:
MJC Biology Department, 435 College Ave, Modesto, CA. 95350, USA
*
1Corresponding author. Email: maddend@mjc.edu. Current address: PO Box 1422, Sutter Creek, California, 95685, USA.

Abstract:

Wild populations of a small neotropical primate, Geoffroy's tamarin (Saguinus geoffroyi), were studied through 30-s instantaneous observational sampling to identify different canopy habitats used by this tamarin. Tree and shrub canopies were sampled in randomly selected plots and in nearby plots that tamarins were observed to use in the forests of Agua Clara, Panama (28 d, 59 100-m2 plots, 32.25 h of tamarin observations, 27 tamarins in total), and in the nearby forests of Barro Colorado Island (49 d, 29 100-m2 plots, 29.6 h of tamarin observations, 14 tamarins in total). Light penetration through the canopy, ambient temperature and humidity, presence of other primates, stem diameters, plant life-forms, distribution of woody flora, abundance of fleshy fruits and arthropods typically consumed by tamarins and abundance of thorny vegetation and biting arthropods in plots used by tamarins were compared with control plots. Habitats used by tamarins had significantly shorter distances between adjacent tree canopies and between canopies and the ground. There was a random distribution of large insects and fleshy fruits that tamarins are known to eat. Habitat selection by tamarins may not be influenced by spiny vegetation, but tamarins may avoid areas with abundant hooked thorns and blood-sucking arthropods. Mobility along runways in various tiers of a rain-forest canopy may be of primary importance, with local abundance of food being a secondary consideration in habitat selection by this small primate.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2010

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References

LITERATURE CITED

BURNHAM, K. P. & ANDERSON, D. R. 2002. Model selection and multimodel inference: a practical information-theoretical approach. Springer-Verlag, New York. 496 pp.Google Scholar
CAINE, N. G. 1993. Flexibility and cooperation as unifying themes in Saguinus social organization and behavior: the role of predator pressures. Pp. 200219 in Rylands, A. B. (ed.). Marmosets and tamarins: systematics, behaviour, and ecology. Oxford University Press, Oxford.CrossRefGoogle Scholar
CROAT, T. B. 1978. Flora of Barro Colorado. Stanford University Press, Stanford.Google Scholar
DEMES, B., JUNGERS, W. L., FLEAGLE, J. G., WUNDERLICH, R. E., RICHMOND, B. G. & LEMELIN, P. 1996. Body size and leaping kinetics in Malagasy vertical clingers and leapers. Journal of Human Evolution 31:367388.CrossRefGoogle Scholar
EMMONS, L. H. & GENTRY, A. H. 1983. Tropical forest structure and the distribution of gliding and prehensile-tailed vertebrates. American Naturalist 121:513524.CrossRefGoogle Scholar
GARBER, P. A. 1980. Locomotor behavior and feeding ecology of the Panamanian tamarin (Saguinus oedipus geoffroyi, callitrichidae, primates). International Journal of Primatology 1:185201.CrossRefGoogle Scholar
GARBER, P. A. 1988. Diet, foraging patterns, and resource defense in a mixed species troop of Saguinus mystax and Saguinus fuscicollis in Amazonian Peru. Behaviour 105:1834.CrossRefGoogle Scholar
GARBER, P. A. 1992. Vertical clinging, small body size, and the evolution of feeding adaptations in the Callitrichinae. American Journal of Physical Anthropology 88:469482.CrossRefGoogle ScholarPubMed
GARBER, P. A. 1993. Feeding, ecology, and behaviour of the genus Saguinus. Pp. 273295 in Rylands, A. B. (ed.). Marmosets and tamarins: systematics, behavior, and ecology. Oxford University Press, Oxford.CrossRefGoogle Scholar
GARBER, P. A. 2000. The ecology of group movement: evidence for the use of spatial, temporal, and social information in some primate foragers. Pp. 261298 in Boinski, S. & Garber, P. A. (eds.). On the move: how and why animals travel in groups. University of Chicago Press, Chicago.Google Scholar
JANZEN, D. H. 1966. Coevolution of mutualism between ants and Acacia in Central America. Evolution 20:249275.CrossRefGoogle ScholarPubMed
KERSHAW, K. M. & LOONEY, J. H. 1985. Quantitative and dynamic plant ecology. Edward Arnold, London.Google Scholar
MADDEN, D. & HARMON, W. 1998. First record and morphology of Myialges caulotoon Acari: Epidermoptidae from Galapagos hosts. Journal of Parasitology 84:186189.CrossRefGoogle ScholarPubMed
MADDEN, D., BALLESTERO, J., CALVO, C., CARLSON, R., CHRISTIANS, E. & MADDEN, E. 2008. Sea turtle nesting as a process influencing a sandy beach ecosystem. Biotropica 40:758765.CrossRefGoogle Scholar
MILEWSKI, A. & MADDEN, D. 2006. Interactions between large mammals and thorny plants on a wildlife ranch in Kenya. African Journal of Ecology 44:515522.CrossRefGoogle Scholar
MILTON, K. & HOPKINS, M. E. 2006. Growth of a reintroduced spider monkey (Ateles geoffroyi) population on Barro Colorado Island, Panama. Pp. 417435 in Estrada, E., Garber, P. A., Pavelka, M. S. & Luecke, L. (eds.). New perspectives in the study of Mesoamerican primates. Springer, New York.CrossRefGoogle Scholar
NICKLE, D. A. & HEYMANN, E. W. 1996. Predation on Orthoptera and other orders of insects by tamarin monkeys, Saguinus mystax and Saguinus fuscicollis (Primates: Callitrichidae), in Northeastern Peru. Journal of Zoology 239:799819.CrossRefGoogle Scholar
NUNN, C. L. & HEYMANN, E. W. 2005. Malaria infection and host behavior: a comparative study of neotropical primates. Behavioral Ecology and Sociobiology 59:3037.CrossRefGoogle Scholar
PERES, C. A. 1991. Ecology of mixed-species groups of tamarins in Amazonina terra firme forests. PhD thesis, University of Cambridge, Cambridge, UK.Google Scholar
PERES, C. A. 1993. Structure and spatial organization of an Amazonian terra firme forest primate community. Journal of Tropical Ecology 9:259276.CrossRefGoogle Scholar
POORTER, L., BONGERS, L. & BONGERS, F. 2006. Architecture of 54 moist-forest tree species: traits, trade-offs, and functional groups. Ecology 87:12891301.CrossRefGoogle ScholarPubMed
PUTZ, F. E. & WINDSOR, D. 1987. Liana phenology on Barro Colorado Island, Panama. Biotropica 9:334341.CrossRefGoogle Scholar
RYLANDS, A. B., DA CRUZ, O. M. & FERRARI, S. F. 1989. An association between marmosets and army ants in Brazil. Journal of Tropical Ecology 5:113116.CrossRefGoogle Scholar
SANFORD, R. L., BRAKER, H. E. & HARTSHORN, G. S. 1986. Canopy openings in a neotropical lowland forest. Journal of Tropical Ecology 2:277282.CrossRefGoogle Scholar
SCHNITZER, S. A. & CARSON, W. P. 2001. Treefall gaps and the maintenance of species diversity in a tropical forest. Ecology 82:913919.CrossRefGoogle Scholar
SMITH, A. C. 2000. Interspecific differences in prey captured by associating saddleback (Saguinus fuscicollis) and moustached (Saguinus mystax) tamarins. Journal of Zoology 251:315324.CrossRefGoogle Scholar
SUEN, H. K. & ARY, D. 1984. Variables influencing one-zero and instantaneous time sampling outcomes. Primates 25:8994.CrossRefGoogle Scholar
WILSON, N., DIETZ, J. M. & WHITAKER, J. 1989. Ectoparasitic acari found on golden lion tamarins (Leontopithecus rosalia rosalia) from Brazil. Journal of Wildlife Diseases 25:433435.CrossRefGoogle ScholarPubMed