Skip to main content
Log in

Intraspecific Variation in the Mating System of Spectral Tarsiers

  • Published:
International Journal of Primatology Aims and scope Submit manuscript

Abstract

Historically, a species’ social system was perceived to be a fixed attribute and deviations were usually treated as aberrant or maladaptive. Over the last few decades, socioecologists have started to recognize that variation in social systems is normal and adaptive. Here I explore how ecological variation affects the mating system of a nocturnal primate, the spectral tarsier, Tarsius spectrum. Several studies of the spectral tarsier have illustrated variation in this species’ mating system. Although most groups exhibit a monogamous mating system, a small proportion of the population consistently exhibits a polygynous mating system. I conducted this study at Tangkoko Nature Reserve in Sulawesi, Indonesia during 2007. I found that group size was highly variable, ranging from 2 individuals to as many as 8 individuals per sleeping site. Although most groups (21 of 26) were composed of a single adult male and a single adult female, ca. 19% of the groups contained 2 adult females. Three of the 5 groups with 2 adult females contained 2 young infants. As might be expected, polygynous groups were larger than were monogamous groups. The mean group size of monogamous groups was 2.9, whereas the mean group size of polygynous groups was 6.0. Polygynous groups were also more likely to use Ficus caulocarpa trees than were the monogamous groups. Polygynous groups consistently used more sleeping sites as well as larger diameter sleeping trees, than did monogamous groups. The large-diameter fig trees are ideal homes for the spectral tarsiers in that they offer multiple entrances and exits as well as protection from the elements. Polygynous and monogamous groups exhibited no differences in insect biomass available, home range size, or height of sleeping tree. These results support the hypothesis that ecological variation is an important determinant of mating system within spectral tarsiers.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Altmann, J. (1974). Observational study of behavior: sampling methods. Behaviour, 49, 227–267.

    Article  CAS  PubMed  Google Scholar 

  • Audley-Charles, M. (1981). Geological history of the region of Wallace’s Line. In T. C. Whitmore (Ed.), Wallace’s line and plate tectonics. Oxford: Clarendon Press.

    Google Scholar 

  • Bibby, R., Southwood, T., & Cairns, P. (1992). Techniques for estimating population density in birds. New York: Academic Press.

    Google Scholar 

  • Brower, J., Zar, J., & von Ende, C. (1990). Field and laboratory methods for general ecology. Ames, IA: Wm. C. Brown.

    Google Scholar 

  • Brown, J. (1964). The evolution of diversity in avian territorial systems. Wilson Bulletin, 76, 160–169.

    Google Scholar 

  • Brown, J., Dow, D., Brown, E., & Brown, S. (1983). Socioecology of the grey-crowned babbler: population structure, unit size and vegetation correlates. Behavioral Ecology and Sociobiology, 13, 115–124.

    Article  Google Scholar 

  • Campbell, P. (2008). The relationship between roosting ecology and degree of polygyny in harem-forming bats: perspectives from Cynopterus. Journal of Mammalogy, 89, 1351–1360.

    Article  Google Scholar 

  • Chapman, C., & Rothman, J. M. (2009). Within-species differences in primate social structure: evolution of plasticity and phylogenetic constraints. Primates, 50, 12–22.

    Article  PubMed  Google Scholar 

  • Chaverri, G., Gamba-Rios, M., & Kunz, T. (2007). Range overlap and association patterns in the tent-making bat Artibeus watsoni. Animal Behaviour, 73, 157–164.

    Article  Google Scholar 

  • Davies, N. B., & Lundberg, A. (1984). Food distribution and a variable mating system in the dunnock, Prunella modularis. The Journal of Animal Ecology, 53, 895–912.

    Article  Google Scholar 

  • Della Sala, D. (1985). The yellow warbler in southeastern Michigan: factors affecting its productivity. Jack-Pine Warbler, 63, 1–10.

    Google Scholar 

  • Emlen, S., & Orings, L. (1977). Ecology, sexual selection and the evolution of mating systems. Science, 197, 215–223.

    Article  CAS  PubMed  Google Scholar 

  • Freed, L. (1986). Usurpatory and opportunistic bigamy in tropical house wrens. Animal Behaviour, 34, 1894–1896.

    Article  Google Scholar 

  • Gill, F. B., & Wolf, L. (1975). Economics of feeding territoriality in the golden winged sunbird. Ecology, 56, 333–345.

    Article  Google Scholar 

  • Gursky, S. (1995). Group size and composition. Tropical Biodiversity, 3(1), 57–62.

    Google Scholar 

  • Gursky, S. (1997). Modeling maternal time budgets: The impact of lactation and gestation on the behavior of the spectral tarsier, Tarsius spectrum. Ph.D. dissertation, SUNY-Stony Brook.

  • Gursky, S. (1998). Conservation status of the spectral tarsier Tarsius spectrum: Population density and home range size. Folia Primatologica, 69, 191–203.

    Article  Google Scholar 

  • Gursky, S. (2000). The effect of seasonality on the behavior of an insectivorous primate, Tarsius spectrum. International Journal of Primatology, 21, 477–495.

    Article  Google Scholar 

  • Gursky, S. (2003). The effect of moonlight on a nocturnal prosimian primates. International Journal of Primatology, 24, 351–367.

    Article  Google Scholar 

  • Gursky, S. (2006). Function of snake mobbing in spectral tarsiers. American Journal of Physical Anthropology, 129, 601–608.

    Article  PubMed  Google Scholar 

  • Gursky, S. (2007). The spectral tarsiers. In N. Vasey & R. Sussman (Eds.), Primate field studies series. Upper Saddle River, NJ: Prentice-Hall.

    Google Scholar 

  • Gursky, S. (in press). Dispersal by a nocturnal prosimian. International Journal of Primatology.

  • Janzen, D. (1973). Sweep samples of tropical foliage insects: effects of seasons, vegetation types, elevation, time of day and insularity. Ecology, 54(3), 687–708.

    Article  Google Scholar 

  • Jouventin, P., & Cornet, A. (1979). Social life of seals. Recherche, 10, 1058–1066.

    Google Scholar 

  • Kappeler, P. (2000). Causes and consequences of unusual sex ratios among lemurs. In P. M. Kappeler (Ed.), Primate males (pp. 55–63). Cambridge: Cambridge University Press.

    Google Scholar 

  • Kenward, R. (1987). Wildlife radio tagging. New York: Academic Press.

    Google Scholar 

  • Kleiman, D. G. (1977). Monogamy in mammals. Revue de Biologie, 52, 39–69.

    Article  CAS  Google Scholar 

  • Kutsukake, M., & Nunn, C. L. (2006). Comparative tests of reproductive skew in male primates: the roles of demographic factors and incomplete control. Behavioral Ecology and Sociobiology, 60, 695–706.

    Article  Google Scholar 

  • MacKinnon, J., & MacKinnon, K. (1980). The behavior of wild spectral tarsiers. International Journal of Primatology, 1, 361–379.

    Article  Google Scholar 

  • Moehlman, P. (1989). Intraspecific variation in canid social system. In J. Gittkeman (Ed.), Carnivore behavior, ecology and evolution (pp. 143–163). Ithaca: Cornell University Press.

    Google Scholar 

  • Muirhead-Thomson, R. C. (1991). Trap responses of flying insects. New York: Academic Press.

    Google Scholar 

  • Musser, G. (1987). The mammals of Sulawesi. In T. C. Whitmore (Ed.), Biogeographical evolution of the Malay Archipelago. Oxford: Clarendon Press.

    Google Scholar 

  • Niemitz, C. (1984). Biology of tarsiers. Stuttgart: Gustav Fischer.

    Google Scholar 

  • Nietsch, A., & Niemitz, C. (1992). Indication for facultative polygamy in free-ranging Tarsius spectrum, supported by morphometric data. International Primatological Society abstracts, Strasbourg, p. 318.

  • Orians, G. H. (1969). On the evolution of mating systems in birds and mammals. The American Naturalist, 103, 589–603.

    Article  Google Scholar 

  • Pochron, S., & Wright, P. C. (2003). Variability in adult group compositions of a prosimian primate. Behavioral Ecology and Sociobiology, 54, 285–293.

    Article  Google Scholar 

  • Pope, T. (1991). Effects of demographic change on on group kin structure and gene dynamics of populations of red howling monkeys. Journal of Mammalogy, 79, 692–712.

    Article  Google Scholar 

  • Price, F., & Bock, C. (1973). Polygyny in the dipper. Condor, 75, 457–459.

    Article  Google Scholar 

  • Prohl, H. (2002). Population differences in female resource abundance, adult sex ratio, and male mating success in Dendrobates pumilio. Behavioral Ecology, 13, 175–181.

    Article  Google Scholar 

  • Richards, A. (1974). Intra-specific variation in the social organization and ecology of Propithecus verreauxi. Folia Primatologica, 22, 172–207.

    Google Scholar 

  • Rivas, J., & Burghardt, G. (2005). Snake mating systems, behavior, and evolution: the revisionary implications of recent findings. Journal of Comparative Psychology, 119, 447–454.

    Article  PubMed  Google Scholar 

  • Robbins, M. (2001). A demographic analysis of male life history and social structure of mountain gorillas. Behaviour, 131, 21–47.

    Google Scholar 

  • Said, S., Gaillard, J., Widmer, O., Debias, F., Bourgoin, G., Delorme, D., et al. (2009). What shapes intra-specific variation in home range size? A case study of female roe deer. Oikos, 188, 1299–1306.

    Article  Google Scholar 

  • Sinha, A. (2005). Not in their genes: phenotypic flexibility, behavioral traits and cultural evolution. Journal of Biosciences, 30, 51–64.

    Article  PubMed  Google Scholar 

  • Sokal, R., & Rohlf, J. (1981). Biometry. New York: W. H. Freeman.

    Google Scholar 

  • Southwood, T. R. E. (1992). Ecological methods with particular reference to the study of insect populations. New York: Chapman and Hall.

    Google Scholar 

  • Stacey, P., & Ligon, D. (1987). Territory quality and dispersal options in the acorn woodpecker, and a challenge to the habitat saturation model of cooperative breeding. The American Naturalist, 130, 654–676.

    Article  Google Scholar 

  • van Belle, S., & Estrada, A. (2006). Demographic features of Alouatta pigra populations in extensive and fragmented forests. In A. Estrada, P. A. Garber, M. S. M. Pavelka, & L. Leucke (Eds.), New perspectives in the study of Mesoamerican primates (pp. 121–144). New York: Springer.

    Chapter  Google Scholar 

  • Verdolin, J. (2007). Resources, not male mating strategies, are a determinant of social structure in Gunnison’s prairie dogs (Cynomys gunnisoni). Behaviour, 144, 1361–1382.

    Article  Google Scholar 

  • Walker, F. M., Taylor, A. C., & Sunnucks, P. (2006). Does soil type drive social organization in southern hairy-nosed wombats? Molecular Ecology, 16, 199–208.

    Article  Google Scholar 

  • Watanabe, K. (1981). Variations in group composition and population density of the two sympatric Mentawaian leaf monkeys. Primates, 22, 145–160.

    Article  Google Scholar 

  • White, G., & Garrott, R. (1987). Analysis of wildlife radiotracking data. New York: Academic Press.

    Google Scholar 

  • Whitmore, T. C. (1984). Wallace’s line and plate tectonics. Oxford: Clarendon Press.

    Google Scholar 

  • Whitten, T., Mustafa, M., & Henderson, G. (1987). The ecology of Sulawesi. Yogyakarta: Gadjah Mada University Press.

    Google Scholar 

  • World Wildlife Fund. (1980). Cagar Alam Gunung Tangkoko Dua Saudara Sulawesi Utara management plan 1981–1986. Bogor, Indonesia: World Wildlife Fund.

    Google Scholar 

  • Wright, P. (1999). Lemur traits and Madagascar ecology: coping with an island environment. Yearbook of Physical Anthropology, 43, 31–72.

    Article  Google Scholar 

  • Yamagiwa, J., Kahekwa, J., & Basabose, A. (2003). Intra-specific variation in social organization of gorillas: implications for their social evolution. Primates, 44, 359–369.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

The methods utilized in this study were reviewed and approved by Texas A&M University IACUC committee. In addition, I obtained permits from the Indonesian Institute of Sciences, and the research complied with the laws of Indonesia. Funding for this research was provided by: Primate Conservation Inc., Conservation International Primate Action Fund, and Texas A&M University. I thank the Indonesian Institute of Sciences (LIPI), the Directorate General for Nature Preservation, and Forest Protection (PHPA) in Manado, Bitung, Tangkoko, and Jakarta, SOSPOL, POLRI, the University of Indonesia, Jatna Supriatna, and Andayani Noviar for their sponsorship while in Indonesia. Special thanks go to my field assistants, Ben and Felik, for their help in collecting the data. I also thank the time and effort the reviewers and the editor spent in improving this article.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sharon Gursky-Doyen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gursky-Doyen, S. Intraspecific Variation in the Mating System of Spectral Tarsiers. Int J Primatol 31, 1161–1173 (2010). https://doi.org/10.1007/s10764-010-9450-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10764-010-9450-2

Keywords

Navigation

pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy