1988
DOI: 10.1016/s0003-3472(88)80262-8
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Effects of age and sex on intra-group spacing behaviour in juvenile savannah baboons, Papio cynocephalus cynocephalus

Abstract: Twenty juvenile members of known genealogies in two baboon groups were studied over a 16month period to evaluate a number of predictions about juvenile spacing behaviour based on the natural history of savannah baboons. Young juveniles (1-2.5 years old) approached more frequently and spent more time in proximity to other group members than did old juveniles (3-5.5 years old). In particular, young juveniles associated more closely with their mothers, particular adult males (possible fathers) and age-peers than … Show more

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Cited by 64 publications
(67 citation statements)
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“…Natal male kin are therefore more concentrating into younger juvenile and sub-adult categories, while female kin remain distributed across a wider range of ages. Age proximity, and particularly peer group membership, is an important regulator of social interactions in capuchins (Schoof & Jack, 2014) and various other animals: gazelles (Walther, 1972), impalas (Murray, 1981), savannah baboons (Pereira, 1988;Alberts, 1999;Silk et al, 2006Silk et al, , 2010, rhesus macaques (Janus, 1992;Widdig et al, 2001Widdig et al, , 2002, chimpanzees (Mitani, 2009), humpback whales (Ramp et al, 2010), and giraffes: (Bercovitch & Berry, 2013). In species featuring high male reproductive skew during brief tenures, such as rhesus macaques, strong associations with peers can allow for different treatment of paternal half siblings as compared to more distant kin (Altmann, 1979;Widdig, 2007Widdig, , 2013.…”
Section: Discussionmentioning
confidence: 99%
“…Natal male kin are therefore more concentrating into younger juvenile and sub-adult categories, while female kin remain distributed across a wider range of ages. Age proximity, and particularly peer group membership, is an important regulator of social interactions in capuchins (Schoof & Jack, 2014) and various other animals: gazelles (Walther, 1972), impalas (Murray, 1981), savannah baboons (Pereira, 1988;Alberts, 1999;Silk et al, 2006Silk et al, , 2010, rhesus macaques (Janus, 1992;Widdig et al, 2001Widdig et al, , 2002, chimpanzees (Mitani, 2009), humpback whales (Ramp et al, 2010), and giraffes: (Bercovitch & Berry, 2013). In species featuring high male reproductive skew during brief tenures, such as rhesus macaques, strong associations with peers can allow for different treatment of paternal half siblings as compared to more distant kin (Altmann, 1979;Widdig, 2007Widdig, , 2013.…”
Section: Discussionmentioning
confidence: 99%
“…Second, fathers may help offspring attain a higher quality and/or quantity of food; in Rhesus macaques, juveniles with persistent relationships with adult males (whose paternal status was unknown) gained greater access to food resources (37). This form of paternal care may be beneficial if offspring forage near their fathers and are thereby protected from feeding interruptions or if proximity to fathers helps them gain access to better food sources through observational learning of food types or foraging skills (38)(39)(40). Food acquisition influences both growth rates and age at maturity in a number of primate species (41,42), including baboons (35,43), and could be a major mediator of the paternal effects documented here.…”
Section: Discussionmentioning
confidence: 99%
“…However, owing to the high skew in male reproduction found in many species [5,25], paternal siblings tend to be born in the same age cohort [26]. As age mates go through the same life-history stages at the same time, they can be found to preferentially interact with each other [27,28]. Age proximity was therefore suggested (at least) as a primary mechanism for paternal kin recognition [17,18].…”
Section: Introductionmentioning
confidence: 99%