Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-75dct Total loading time: 0 Render date: 2024-05-01T02:33:39.350Z Has data issue: false hasContentIssue false

7 - Trapping primates

Published online by Cambridge University Press:  05 June 2012

Joanna M. Setchell
Affiliation:
University of Durham
Deborah J. Curtis
Affiliation:
Oxford Brookes University
Get access

Summary

INTRODUCTION

There are many reasons to capture study animals. They include marking or radio-collaring (Chapter 10), taking morphological measurements (Chapter 9), or biological samples (Chapters 1 and 8), and estimating age and condition. For small nocturnal primates, capture is essential to radio-tag animals for direct observation, the most effective method of determining the spatial distribution and social interactions of individuals and estimating population densities (Chapter 6; Sterling et al., 2000). Historically, studies in which wild, larger-bodied, primates are habituated for long-term observation have rarely included capture, perhaps because researchers have been understandably wary of its effects on subsequent behaviour and habituation (Chapters 2 and 11). However, a survey of more than 120 studies that combined observation with capture, and which involved about 65 primate species, showed that a careful capture–release programme using trapping will not cause a previously habituated population to change its behaviour towards human observers, and will not be associated with excess mortality or serious injury (Jolly & Phillips-Conroy, 1993 and unpublished data). Changes in ranging habits will be temporary at worst, and basic social organization and structure will not be affected. The survey also provided a comparison between capture methods. Trapping has been used most often to catch diurnal-terrestrial and nocturnal-arboreal species. Diurnal-arboreal primates (apart from callitrichines) have generally been captured by darting (Chapter 8), a bias that seems unjustified.

Type
Chapter
Information
Field and Laboratory Methods in Primatology
A Practical Guide
, pp. 133 - 146
Publisher: Cambridge University Press
Print publication year: 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ancrenaz, M., Lackman-Ancrenaz, I. & Mundy, N. (1994). Field observations of aye-aye (Daubentonia madagascariensis) in Madagascar. Folia Primatol. 62, 22–36.CrossRefGoogle Scholar
Albernaz, A. L. & Magnusson, W. E. (1999). Home-range size of the bare-ear marmoset (Callithrix argentata) at Alter do Chão, Central Amazonia, Brazil. Int. J. Primatol. 20, 665–77.CrossRefGoogle Scholar
Atsalis, S. (1999). Seasonal fluctuations in body fat and activity levels in a rain-forest species of mouse lemur, Microcebus rufus. Int. J. Primatol. 20, 883–910.CrossRefGoogle Scholar
Biebouw, K. (2009). Home range size and use in Allocebus trichotis in Analamazaotra Special Reserve, Central Eastern Madagascar. Int. J. Primatol. 30, 367–86.CrossRefGoogle Scholar
Brett, F. L., Turner, T. R., Jolly, C. J. & Cauble, R. G. (1982), Trapping baboons and vervet monkeys from wild, free-ranging populations. J. Wildlife Manag. 46, 164–74.CrossRefGoogle Scholar
Charles-Dominique, P. (1977). Ecology and Behaviour of Nocturnal Primates. London: Duckworth.Google Scholar
Charles-Dominique, P. & Bearder, S. K. (1979). Field studies of lorisid behavior: Methodological aspects. In The Study of Prosimian Behavior, ed. Doyle, G. A. & Martin, R. D., pp. 567–629. New York: Academic Press.CrossRefGoogle Scholar
Dawson, G. A. (1977). Composition and stability of social groups of the tamarins (Saguinus oedipus geoffroyi) in Panama: ecological and behavioral implications. In The Biology and Conservation of the Callitrichidae, ed. Kleiman, D. G., pp. 23–8. Washington, D.C.: Smithsonian Press.Google Scholar
Ruiter, J. (1992). Capturing wild long-tailed macaques (Macaca fascicularis). Folia Primatol. 59, 89–104.CrossRefGoogle Scholar
Dietz, J. M., Baker, A. J. & Miglioretti, D. (1994). Seasonal variation in reproduction, juvenile growth, and adult body mass in golden lion tamarins (Leontopithecus rosalia). Am. J. Primatol. 34, 115–32.CrossRefGoogle Scholar
Ehresmann, P. (2000). Ökologische Differenzierung von zwei sympatrischen Mausmaki-Arten (Microcebus murinus und M. ravelobensis) im Trockenwald Nordwest-Madagaskars. PhD thesis, University of Hanover.
Fietz, J. (1999). Mating system of Microcebus murinus. Am. J. Primatol. 48, 127–33.3.0.CO;2-4>CrossRefGoogle ScholarPubMed
Fietz, J. & Ganzhorn, J. U. (1999). Feeding ecology of the hibernating primate Cheirogaleus medius: how does it get so fat? Oecologica 121, 157–64.CrossRefGoogle ScholarPubMed
Garber, P. A., Encarnación, F., Moya, L. & Pruetz, J. D. (1993). Demographic and reproductive patterns in moustached tamarin monkeys (Saguinus mystax): implications for reconstructing platyrrhine mating systems. Am. J. Primatol. 29, 235–54.CrossRefGoogle Scholar
Gursky, S. (2000). Sociality in the spectral tarsier, Tarsius spectrum. Am. J. Primatol. 51, 89–101.3.0.CO;2-7>CrossRefGoogle ScholarPubMed
Jansen, K. L. (2000). A review of the nonmedical use of ketamine: use, users and consequences. J. Psychoactive Drugs. 32, 419–33.CrossRefGoogle ScholarPubMed
Jolly, C. J. (1998). A simple and inexpensive pole syringe for tranquilizing primates. Lab. Primate Newsl. 37, 1–2.Google Scholar
Jolly, C. J. & Phillips-Conroy, J. E. (1993). The use of capture in field primatology. Am. J. Phys. Anthropol. Suppl.16, 158.Google Scholar
Kappeler, P. M. (1997). Intrasexual selection in Mirza coquereli: evidence for scramble competition in a solitary primate. Behav. Ecol. Sociobiol. 45, 115–27.CrossRefGoogle Scholar
Lahann, P. (2007). Biology of Cheirogaleus major in a littoral rainforest in southeast Madagascar. Int. J. Primatol. 28, 895–905.CrossRefGoogle Scholar
Melnick, D. J., Pearl, M. C. & Richard, A. F. (1984). Male migration and inbreeding avoidance in wild rhesus monkeys. Am. J. Primatol. 7, 229–43.CrossRefGoogle Scholar
Müller, A. E. (1999). Aspects of social life in the fat-tailed dwarf lemur (Cheirogaleus medius): inferences from body weights and trapping data. Am. J. Primatol. 49, 265–80.3.0.CO;2-U>CrossRefGoogle ScholarPubMed
Petter, J. J. & Hladik, C. M. (1970). Observations sur le domaine vital et la densité de population de Loris tardigradus dans les forêts de Ceylan. Mammalia 34, 394–409.CrossRefGoogle Scholar
Petter, J. J. & Peyrieras, A. (1970). Nouvelle contribution à l'étude d'un lémurien malgache, le aye-aye (Daubentonia madagascariensis E. Geoffroy). Mammalia 34, 167–93.CrossRefGoogle Scholar
Savage, A., Giraldo, H., Blumer, E. S.et al. (1993). Field techniques for monitoring cotton-top tamarins (Saguinus oedipus oedipus) in Columbia. Am. J. Primatol. 31, 189–96.CrossRefGoogle Scholar
Schülke, O. & Kappeler, P. M. (2003). So near and yet so far: territorial pairs but low cohesion between pair partners in a nocturnal lemur, Phaner furcifer. Anim. Behav. 65, 331–43.CrossRefGoogle Scholar
Schwab, D. (2000). A preliminary study of spatial distribution and mating system of pygmy mouse lemurs (Microcebus cf. myoxinus). Am. J. Primatol. 51, 41–60.3.0.CO;2-7>CrossRefGoogle Scholar
Silveira, G., Bicca-Marques, J. C. & Nunes, C. A. (1998). On the capture of titi monkeys (Callicebus cupreus) using the Peruvian method. Neotropical Primates 6, 114–15.Google Scholar
Sterling, E. J., Nguyen, N. & Fashing, P. J. (2000). Spatial patterning in nocturnal prosimians: a review of methods and relevance to studies of sociality. Am. J. Primatol. 51, 3–19.3.0.CO;2-D>CrossRefGoogle ScholarPubMed
Wiens, F. (2002). Behavior and ecology of wild slow lorises (Nycticebus coucang): social organization, infant care system, and diet. PhD thesis, University of Bayreuth.
Wright, P. C. & Martin, L. B. (1995). Predation, pollination and torpor in two nocturnal prosimians: Cheirogaleus major and Microcebus rufus in the rain forest of Madagascar. In Creatures of the Dark: The Nocturnal Prosimians, ed. Alterman, L., Doyle, G. A. & Izard, M. K., pp. 45–60. New York: Plenum Press.CrossRefGoogle Scholar
Zingg, J. (2001). Nahrungsökologie und Sozialverhalten von Zwergseidenäffchen (Cebuella pygmaea) in Ecuador. Diploma thesis, University of Zurich.

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×