We carried out a survey on roadside dark-bellied bonnet macaques (Macaca radiata radiata) on the highways around the south Indian city of Mysore. The present survey was the fourth since 1989 on the same populations. We divided the habitats into intensive cultivation (IC), wet cultivation (WC), and scrub forests (SC). The number of groups has significantly reduced from 54 to 31 and the number of animals has declined from 1,207 to 697 from 1989 to 2009. This decline has been recorded only in the IC and WC areas, whereas the population in SC with places of Hindu worship has remained stable. Due to the loss of roadside Ficus trees over the years, the habitat of the monkeys has almost disappeared. Since bonnet macaque is not primarily a forest-dwelling species, the seemingly widespread primate may soon become 'threatened' if the non-forest populations continue to decline. Scrub forests in small hillocks housing Hindu temples remain the only prospective places for conservation of bonnet macaques.
The distribution and availability of food was examined to see how it influenced ranging patterns and sleeping site selection in a group of lion-tailed macaques. The home range and core area were 130.48 ha (95% kernel) and 26.68 ha (50% kernel) respectively. The lion-tailed macaques had a longer day range, had a greater number of sleeping sites and used more core areas in the summer as compared to the monsoon and the post-monsoon seasons. The ranging patterns and sleeping site use were influenced by the major food resources used in a particular season. The ranging was mainly influenced by Artocarpus heterophyllus in monsoon, Cullenia exarillata and Toona ciliata in post- monsoon, and Artocarpus heterophyllus and Ficus amplissima in summer. The distribution of these four plant species is, therefore, critical to ranging, and thus to conservation of the lion-tailed macaque.
Folivory, being a dietary constraint, can affect the social time of colobines. In the present study, we compared food items and activity budgets of two closely related species of colobines inhabiting South India, i.e. the Hanuman langur (Semnopithecus hypoleucos) and Nilgiri langur (Semnopithecus johnii), to determine whether folivory had an impact on social time in these species. Our study established that Nilgiri langurs were more folivorous than Hanuman langurs. Nilgiri langurs spent much less time on social activities, but more time on resting, although the social organization of S. hypoleucos was similar to that of the Nilgiri langur. The enforced resting time for fermentation of leafy food items may have reduced the time available for social interactions, which in turn affected the social time in Nilgiri langurs. By comparing the data from previous studies on other Hanuman langur species, we found that S. hypoleucos spent a similar amount of time on social activities as Semnopithecus entellus. Hence, the social behaviour of S. entellus and S. hypoleucos is phylogenetically highly conservative.
Studies that compare differences in the behavioural variability across species and genera are rare among south Asian primates. Such studies are important for understanding within-group feeding competition in primates as interindividual difference in frequency of behaviour is a good indicator of feeding competition. We compared the variability in individual activities of lion-tailed macaques, bonnet macaques, Nilgiri langurs, and black-footed grey langurs. Both macaque species showed variability in their activities, with bonnet macaques showing higher variability than lion-tailed macaques. This indicated higher within-group competition in bonnet macaques than in lion-tailed macaques. Folivorous Nilgiri langurs and black-footed grey langurs did not show variability in any behaviour, indicating weak or negligible within-group competition. Except in the bonnet macaque, the interindividual differences in activities in the other species were potentially due to the differences between lactating and non-lactating females. We observed that langurs were less variable than macaques, indicating higher within-group competition in macaques than in langurs. We also observed a higher frequency of aggressive interactions during feeding among macaques than langurs, substantiating higher within-group competition in macaques than in langurs. We further discuss the different possibilities of within-group contest and scramble competition in these species.
Life history traits evolve such that the reproductive output of an organism is maximized. Demographic characteristics, a consequence of life history traits, indicate the reproductive output per individual in group-living species. Both phylogenetic and ecological factors influence demographic traits. In the forests of the Western Ghats, India, we studied the demography of three langur species: Semnopithecus johnii, a wet forest-dwelling species; Semnopithecus hypoleucos, largely a wet forest-dwelling species; and Semnopithecus priam, a primarily dry forest-dwelling species. S. hypoleucos and S. priam are genetically closer to each other than to S. johnii. We sampled a total of 193 groups of the three species of langurs. The group size was smaller in the two wet forest-dwelling species, S. johnii (median = 10) and S. hypoleucos (nine), than in the dry forest-dwelling species, S. priam (18). The number of adult females per group was higher in S. priam (seven) and S. johnii (six) than in S. hypoleucos (four). On the other hand, the adult female:immature ratio, indicating reproductive output and life history, was highest in S. johnii (1:0.33) followed by S. hypoleucos (1:1) and S. priam (1:1.09). Our results suggest that reproductive output is lowest in the arboreal wet forest species and increases as the species become somewhat dry deciduous forest dwellers, or almost facultative dry forest dwellers, and relatively more terrestrial. Some traits, such as group size, appear to be more sensitive to ecological factors, and some other traits such as age-sex ratios and reproductive output appear to be more conservative.
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