Spider monkeys (Ateles spp.) are well known for their highly arboreal lifestyle, spending much of their time in the highest levels of the canopy and rarely venturing to the ground. To investigate terrestriality by Ateles and to illuminate the conditions under which spider monkeys venture to the ground, we analyzed ad libitum data from 5 study sites, covering 2 species and 5 subspecies.
belzebuth).Terrestrialism by Ateles at all sites is rare; however, it is more restricted at the 2 South American sites. In South America, ground use only occurred in the contexts of eating soil or rotten wood and visiting salt licks. In contrast at the 3 sites with Ateles geoffroyi it rarely occurred in a feeding context, but instead more frequently while drinking from streams during the dry season, by adult females escaping attack by adult males, and as part of a chase C a m p b e l l e t a l . i n I n t e r n a t I o n a l J o u r n a l o f P r I m a t o l o g y 2 6 ( 2 0 0 5 ) 1040 game. In addition, on BCI adult males were on the ground before attacking adult females. We discuss potential explanations, e.g., climate, species differences, predation pressure, for the differences between the Central/North and South American observations.
We report the first evidence of intragroup coalitionary aggression leading to the death of a wild young adult male spider monkey. During a long-term study of a well-habituated community at the Otoch Ma'ax Yetel Kooh reserve in Yucatan, Mexico, a young adult male sustained severe injuries repeatedly between January and March 2002. On 1 April 2002 the same male was the victim of an intragroup attack by at least one adult male that resulted in his death. We highlight several causes of intragroup aggression that may account for the killing.
Animal home ranges may vary little in their size and location in the short term but nevertheless show more variability in the long term. We evaluated the degree of site fidelity of two groups of spider monkeys (Ateles geoffroyi) over a 10- and 13-year period, respectively, in the northeastern Yucatan peninsula, Mexico. We used the Local Convex Hull method to estimate yearly home ranges and core areas (defined as the 60% probability contour) for the two groups. Home ranges varied from 7.7 to 49.6 ha and core areas varied from 3.1 to 9.2 ha. We evaluated the degree of site fidelity by quantifying the number of years in which different areas were used as either home ranges or core areas. Large tracts were used only as home ranges and only for a few years, whereas small areas were used as either core area or home range for the duration of the study. The sum of the yearly core areas coincided partially with the yearly home ranges, indicating that home ranges contain areas used intermittently. Home ranges, and especially core areas, contained a higher proportion of mature forest than the larger study site as a whole. Across years and only in one group, the size of core areas was positively correlated with the proportion of adult males in the group, while the size of home ranges was positively correlated with both the proportion of males and the number of tree species included in the diet. Our findings suggest that spider monkey home ranges are the result of a combination of long-term site fidelity and year-to-year use variation to enable exploration of new resources.
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