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Seasonal, sex, and interspecific differences in activity time budgets and diets of patas monkeys (Erythrocebus patas) and tantalus monkeys (Cercopithecus aethiops tantalus), living sympatrically in northern Cameroon

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Abstract

I examined seasonal, sex, and interspecific differences in activity time budgest and diets of patas (Erythrocebus patas) and sympatric tantalus monkeys (Cercopithecus aethiops tantalus) on the basis of 5-day data sets collected in three and two different seasons, respectively, by the method of focal animal sampling. The seasons included species-specific mating and birth seasons. As compared with not only the birth season but also conspecific females, both patas resident male and tantalus male spent less time feeding and more time resting, day and night, in their respective mating seasons. Given that day-resting time includes time for vigilance for non-resident males and receptive females, this may reflect that males should minimize time spent feeding to allow maximum participation in other fitness-increasing activities such as mating-relating activities asSchoener (1971) predicted. In both species, the males consumed fruits containing less protein but more calories and showed a high feeding rate to compensate for the shorter time spent feeding in the mating season. In contrast, females consumed protein-rich food types (i.e. animals, protein-rich seeds, leaves, and flowers) in the birth season to meet the high demand for protein due to pregnancy and lactation. Given that the season for males was considered to be not a calendar but a reproductive “season” (i.e. mating or birth season), both sexes of patas spent more time moving and less time day- and night-resting than did the tantalus counterparts irrespective of the “season”. Patas subsisted on fruits, gums, and supplementarily lipid-rich seeds as an energy source and animal matters and protein-rich seeds as a protein source. In contrast, tantalus subsisted on fruits and lipid-rich seeds as energy and flowers and leaves as protein.

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References

  • Alberts, S. C.;Altmann, J.;Wilson, M. L. 1996. Mate guarding foraging activity of male baboons.Anim. Behav., 51: 1269–1277.

    Article  Google Scholar 

  • Bicca-Marques, J. C.;Calegaro-Marques, C. 1994. Activity budget and diet ofAlouatta caraya: an age-sex analysis.Folia Primatol., 63: 216–220.

    PubMed  CAS  Google Scholar 

  • Boinski, S. 1988. Sex differences in the foraging behavior of squirrel monkeys in a seasonal habitat.Behav. Ecol. Sociobiol., 23: 177–186.

    Article  Google Scholar 

  • Braza, F.;Alvarez, F.;Azcarate, T. 1983. Feeding habits of the red howler monkeys (Alouatta seniculus) in the Llanos of Venezuela.Mammalia, 47: 205–214.

    Article  Google Scholar 

  • Butynski, T. M. 1988. Guenon birth season and correlates with rainfall and food. In:A Primate Radiation: Evolutionary Biology of the African Guenons,Gautier-Hion,A.;Bourliere,F.;Gautier,J.-P.;Kingdon,J. (eds.), Cambridge Univ. Press, Cambridge, pp. 284–322.

    Google Scholar 

  • Clutton-Brock, T. H. 1977. Some aspects of intraspectific variation in feeding and ranging behaviour in primate. In:Primate Ecology: Studies of Feeding and Ranging Behavior in Lemurs, Monkeys, Apes,Clutton-Brock,T. (ed.), Academic Press, London, pp. 539–556.

    Google Scholar 

  • Clutton-Brock, T. H.;Harvey, P. H. 1977. Species differences in feeding and ranging behaviour in primate. In:Primate Ecology: Studies of Feeding and Ranging Behavior in Lemurs, Monkeys, Apes,Clutton-Brock,T. (ed.), Academic Press, London, pp. 557–579.

    Google Scholar 

  • Cords, M. 1986. Interspecific and intraspecific variation in diet of two forest guenons,Cercopithecus ascanius andC. mitis.J. Anim. Ecol., 55: 811–827.

    Article  Google Scholar 

  • Cronin, J. E.;Sarich, V. M. 1979. Molecular evidence for dual origin of mangabeys among Old World monkeys.Nature, 260: 700–702.

    Article  Google Scholar 

  • Cuthill, I. C.;Macdonald, W. A. 1990. Experimental manipulation of the dawn and dusk chorus in the black birdTurdus merula.Behav. Ecol. Sociobiol., 26: 209–216.

    Article  Google Scholar 

  • Garber, P. A. 1987. Foraging strategies among living primates.Ann. Rev. Anthropol., 16: 339–364.

    Article  Google Scholar 

  • Garber, P. A. 1993. Seasonal patterns of diet and ranging in two species of Tamarin monkeys: stability versus variability.Int. J. Primatol., 14:145–166.

    Article  Google Scholar 

  • Gautier-Hion, A. 1980. Seasonal variations of diet related to species and sex in a community ofCercopithecus monkeys.J. Anim. Ecol., 49: 237–269.

    Article  Google Scholar 

  • Harding, R. S. O;Olson, D. K. 1986. Patterns of mating among male patas monkeys (Erythrocebus patas) in Kenya.Amer. J. Primatol., 11: 343–358.

    Article  Google Scholar 

  • Harrison, M. J. S. 1983. Age and sex difference in the diet and feeding strategies of the green monkey,Cercopithecus sabaeus.Anim. Behav., 31: 969–977.

    Article  Google Scholar 

  • Harrison, M. J. S. 1984. Optimal foraging strategies in the diet of the green monkey,Cercopithecus sabaeus, at Mt. Assirik, Senegal.Int. J. Primatol., 5: 435–471.

    Google Scholar 

  • Harrison, M. J. S. 1985. Time budget of the green monkey,Cercopithecus sabaeus: some optimal strategies.Int. J. Primatol., 6: 351–376.

    Google Scholar 

  • Henzi, S. P.;Lawes, M. 1987. Breeding season influxes and the behaviour of adult male samango monkeys (Cercopithecus mitis albogularis).Folia Primatol., 48: 125–136.

    PubMed  CAS  Google Scholar 

  • Hoffman, S. G. 1983. Sex-related foraging behavior in sequentially hermaphroditic hogfishes (Bodianus spp.).Ecology, 64: 789–808.

    Article  Google Scholar 

  • Isbell, L. A. 1998. Diet for a small primate: insectivory and gummivory in the (large) patas monkeys (Erythrocebus patas pyrrhonotus).Amer. J. Primatol., 45: 381–398.

    Article  CAS  Google Scholar 

  • Isbell, L. A.;Pruetz, J. D.;Lewis, M.;Young, T. P. 1998a. Locomotor activity differences between sympatric vervets (Cercopithecus aethiops) and patas monkeys (Erythrocebus patas): implications for the evolution of long hindlimb length inHomo.Amer. J. Phys. Anthropol., 105: 199–207.

    Article  CAS  Google Scholar 

  • Isbell, L. A.;Pruetz, J. D.;Young, T. P. 1998b. Movements of vervets (Cercopithecus aethiops) and patas monkeys (Erythrocebus patas) as estimators of food resource size, density, and distribution.Behav. Ecol. Sociobiol., 42: 123–133.

    Article  Google Scholar 

  • Isbell, L. A.;Young, T. P. 1993. Social and ecological influences on activity budgets of vervet monkeys, and their implications for group living.Behav. Ecol. Sociobiol., 32: 377–385.

    Article  Google Scholar 

  • Kavanagh, M. 1978. National park in the sahel.Oryx, 14: 241–245.

    Article  Google Scholar 

  • Kavanagh, M. 1983. Birth seasonality inCercopithecus aethiops: a social advantage from synchrony? In:Perspectives in Primate Biology,Seth,P. K. (ed.), Today & Tommorow’s Printers & Publ. Perspect, New Delhi, pp. 89–98.

    Google Scholar 

  • van der Kuyl, A.;Kuiken, C. L.;Dekker, J. T.;Goudsmit, J. 1995. Phylogeny of African monkeys based upon mitochondrial 12S rRNA sequences.J. Mol. Evol., 40: 137–180.

    Google Scholar 

  • Letouzey, R. 1980. Vegetation. In:Atlas of the United Republic of Cameroon,Laclavère G. (ed.), Edit. Jeune Afrique, Paris, pp. 20–24.

    Google Scholar 

  • Meisels, F.;Gautier-Hion, A.;Gautier, J.-P. 1994. Diets of two sympatric colobines in Zaire: more evidence on seed-eating in forests on poor soils.Int. J. Primatol., 15: 681–701.

    Google Scholar 

  • Miquelle, D. G. 1990. Why don’t bull moose eat during the rut?Behav. Ecol. Sociobiol., 27: 145–151.

    Article  Google Scholar 

  • Nakagawa, N. 1989. Activity budget and diet of patas monkeys in Kala Maloue National Park, Cameroon: a preliminary report.Primates, 30: 27–34.

    Article  Google Scholar 

  • Nakagawa, N. 1999. Differential habitat utilization by Patas monkeys (Erythrocebus patas) and Tantalus monkeys (Cercopithecus aethiops tantalus), living sympatrically in Northern Cameroon.Amer. J. Primatol., 49: 243–264.

    Article  CAS  Google Scholar 

  • Napier, J. R.;Napier, P. H. 1967.A Handbook of Living Primates. Academic Press, New York.

    Google Scholar 

  • Ohsawa, H.;Inoue, M.;Takenaka, O. 1993. Mating strategy and reproductive success of male patas monkeys (Erythrocebus patas).Primates, 34: 533–544.

    Article  Google Scholar 

  • Overdorff, D. J. 1993. Similarities, differences, and seasonal patterns in the diet ofEulemur rubriventer andEulemur fulvus rufus in the Ranomafana National Park, Madagascar.Int. J. Primatol., 14: 721–753.

    Article  Google Scholar 

  • Palombit, R. A. 1997. Inter-and intra-specific variation in the diets of sympatric siamang (Hylobates syndactylus) and lar gibbons (Hylobates lar).Folia Primatol., 68: 321–337.

    PubMed  CAS  Google Scholar 

  • Portman, O. W. 1970. Nutritional requirements (NRC) of nonhuman primates. In:Feeding and Nutrition of Nonhuman Primates,Harris,R. S. (ed.), Academic Press, New York, pp. 87–115.

    Google Scholar 

  • Post, D. G.;Hausfater, G.;McCuskey, S. A. 1980. Feeding behavior of yellow baboons (Papio cynocephalus): relationship to age, gender and dominance rank.Folia Primatol., 34: 170–195.

    Article  PubMed  CAS  Google Scholar 

  • Rose, L. M. 1994. Sex differences in diet and foraging behavior in white-faced capuchins (Cebus capucinus).Int. J. Primatol., 15: 95–114.

    Google Scholar 

  • Rowell, T. E.;Richards, S. M. 1979. Reproductive strategies of some African monkeys.J. Mammal, 60: 58–69.

    Article  Google Scholar 

  • Ruvolo, M. 1988. Genetic evolution of the African guenons. In:A Primate Radiation: Evolutionary Biology of the African Guenons,Gautier-Hion,A.;Bourlière,F.;Gautier,J.-P.;Kingdon,J. (eds.), Cambridge Univ. Press, New York, pp. 127–149.

    Google Scholar 

  • Schoener, T. W. 1971. Theory of feeding strategies.Ann. Rev. Ecol. Syst., 11: 369–404.

    Article  Google Scholar 

  • Schoener, T. W. 1974. Resource partitioning in ecological communities.Science, 185: 27–29.

    Article  PubMed  Google Scholar 

  • Silk, J. B. 1987. Activities and feeding behavior of free-ranging pregnant baboons.Int. J. Primatol., 8: 593–613.

    Google Scholar 

  • Symington, M. M. 1988. Demography, ranging patterns, and activity budgets of Black spider monkeys (Ateles paniscus chamek) in the Manu National Park, Peru.Amer. J. Primatol., 15: 45–67.

    Article  Google Scholar 

  • Toft, C. A. 1984. Activity budgets in two species of bee flies (Lordotus: bombyliidae diptera): a comparison of species and sexes.Behav. Ecol. Sociobiol., 14: 287–296.

    Article  Google Scholar 

  • Waterman, P. G. 1984. Food acquisition and processing as a function of plant chemistry. In:Food Acquisition and Processing in Primates,Chivers,D. J.;Wood,B. A.;Bilsoborugh,A. (eds.), Plenum Press, New York, pp. 177–211.

    Google Scholar 

  • Wheatley, B. P. 1982. Energetics of foraging inMacaca fascicularis andPongo pygmaeus and a selective advantage of large body size in the orangutan.Primates, 23: 348–363.

    Article  Google Scholar 

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Nakagawa, N. Seasonal, sex, and interspecific differences in activity time budgets and diets of patas monkeys (Erythrocebus patas) and tantalus monkeys (Cercopithecus aethiops tantalus), living sympatrically in northern Cameroon. Primates 41, 161–174 (2000). https://doi.org/10.1007/BF02557797

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