Resource partitioning and interspecific interactions among sympatric rain forest arboreal mammals of the Western Ghats, India

Resource partitioning in a community of diurnal arboreal mammalsconsisting of the lion-tailed macaque Macaca silenus, bonnetmacaque (BM) Macaca radiata, Nilgiri langur Semnopithecus johnii,and the Indian giant squirrel Ratufa indica of the Western Ghats,southern India, was studied. Differences in their diet, verticalstratification, food resource niche breadth, niche overlap,and behavioral interactions were examined. Resource partitioningwas through differential habitat use, resource use, and verticalstratification. Of the four species, the BM was not a residentspecies and made frequent forays into evergreen forest fromthe adjacent deciduous forest during the flowering season ofCullenia exarillata and fruiting season of Ficus microcarpa.The macaques had narrower niches, and the langur and the squirrelhad wider niches. Niche overlap was highest between the twomacaques. Overlap among the study species was particularly pronouncedduring the flowering of C. exarillata. There was significantcorrelation between niche overlap and intolerance among thestudy species. Certain species pairs showed little or no mutualintolerance despite high overlap. Cooperative interactions suchas alarm calls occurred more frequently among the resident species.Interaction matrices revealed an underlying pattern of interspecificdominance hierarchy, with the BM dominating over the other threespecies. Our study suggests that the BM do not coexist withthe other three because of high overlap with its congener andlow occurrence of cooperative interactions.     

Energy dynamics in the C4 species dominated montane subtropical grassland at Nilgiri Biosphere Reserve, the Western Ghats, India

The energy dynamics in Thiashola grassland, a montane subtropical vegetation in Nilgiri Biosphere Reserve, the Western Ghats, India is studied for a period of one year. The study revealed that the energy content in unit biomass of C₃ and C₄ species has not varied significantly. However, the C₄ species in total due to higher net primary production, entrapped 8.5 times greater solar energy (28.82 kcal/m²/day) than that of their C₃ counterparts. Of the total energy fixed, the C₃ and C₄ species, respectively channeled 4.07 kcal/m²/day and 13.3 kcal/m²/day to the aboveground standing live compartment. The transfer rate of energy to standing dead compartment from standing live part were 3.22 kcal/m²/day and 10.36 kcal/m²/day for C₃ and C₄ species, respectively and both the C₃ and C₄ together transferred 4.81 kcal/m²/day of energy from standing dead to litter compartment. The total dissipation of energy from the system is determined to be 4401.11 kcal/m²/yr and the surplus quantity of 38.37% of energy is accumulated in the aboveground parts of both C₃ and C₄ species which indicates the availability of substantial amount of energetic fodder to the wild herbivores in the Thiashola grassland.     

Energy dynamics in the C4 species dominated montane subtropical grassland at Nilgiri Biosphere Reserve, the Western Ghats, India

The energy dynamics in Thiashola grassland, a montane subtropical vegetation in Nilgiri Biosphere Reserve, the Western Ghats, India is studied for a period of one year. The study revealed that the energy content in unit biomass of C₃ and C₄ species has not varied significantly. However, the C₄ species in total due to higher net primary production, entrapped 8.5 times greater solar energy (28.82 kcal/m²/day) than that of their C₃ counterparts. Of the total energy fixed, the C₃ and C₄ species, respectively channeled 4.07 kcal/m²/day and 13.3 kcal/m²/day to the aboveground standing live compartment. The transfer rate of energy to standing dead compartment from standing live part were 3.22 kcal/m²/day and 10.36 kcal/m²/day for C₃ and C₄ species, respectively and both the C₃ and C₄ together transferred 4.81 kcal/m²/day of energy from standing dead to litter compartment. The total dissipation of energy from the system is determined to be 4401.11 kcal/m²/yr and the surplus quantity of 38.37% of energy is accumulated in the aboveground parts of both C₃ and C₄ species which indicates the availability of substantial amount of energetic fodder to the wild herbivores in the Thiashola grassland.     

Distribution and Abundance of Primates in Rain Forests of the Western Ghats,Karnataka, India and the Conservation of Macaca silenus

We assessed the distribution and abundance of 4 species of diurnal primates viz. lion-tailed macaque, bonnet macaque, Nilgiri langur and Hanuman langur, in 2 areas—Brahmagiri-Makut and Sirsi-Honnavara—in rain forests of the Western Ghats in the state of Karnataka, India. The Nilgiri langurs in Brahmagiri-Makut and the lion-tailed macaques in Sirsi-Honnavara are the northernmost populations of the 2 species in the Western Ghats. The 2 regions represent changes in ecological zones in the Western Ghats. In Brahmagiri-Makut, Hanuman langurs and bonnet macaques occupy lower elevations whereas Nilgiri langurs live in relatively higher altitudes. Only one group of lion-tailed macaques was in Brahmagiri-Makut. In the forests of Sirsi-Honnavara, 3 species of primates viz. lion-tailed macaque, bonnet macaque and Hanuman langur were in larger numbers throughout the forest. A self-sustainable single population of 32 groups of lion-tailed macaques occurred in Sirsi-Honnavara. Few subspecies of Hanuman langurs exist in the study regions. Due to local hunting practices, the relative abundance of primates in Brahmagiri-Makut is lower than that in Sirsi-Honnavara.     

Group fission in Nilgiri langurs (Presbytis johnii)

During a field study on habituated groups of wild Nilgiri langurs (Presbytis johnii),four cases of group fission were observed which differed markedly from group changes reported in other species of the same genus. All fissions occurred in groups with more than one mature male and roughly coincided with the onset of loud call vocalization by the second mature male group member. As a result of the fission the founder group factions acquired the structure of a onemale group. The filial factions consisted of both mature males and females and occupied, at least temporarily, a part of, or an area adjacent to, the founder group. During fission, the amount of aggressive interactions between the two mature males increased. However, the majority of agonistic interactions involved ritualized threat and intimidation behavior without physical aggression. In at least three cases the two mature males involved in the fission had not joined recently but had lived in these groups for three years or more. Although the presence of all male bands and single males in the two study populations indicate that male replacement by invasive takeovers may occur, it is suggested that in Nilgiri langurs, noninvasive fissions are probably another common mechanism for the foundation and maintenance of bisexual one-male groups.     

Loud calls of male Nilgiri langurs (Presbytis johnii): Age-, individual-, and population-specific differences

Adult male Nilgiri langurs (Presbytis johnii) utter loud call bouts consisting of one or more phrases. Phrases are made up of several units showing similar or different structural features. The units involved differ with respect to not only their physical structure but also their overall utilization: three vocal patterns are uttered exclusively by mature males living in bisexual groups or all-male bands and, in addition to being part of loud call bouts, are given during encounters with terrestrial predators; two vocal patterns are uttered by males and females, again not just as constituents of loud calls; and one vocal pattern is given exclusively by mature males living in bisexual groups. Within a given bout, phrases differ not only with respect to their composition but also in their temporal organization. In addition to the acoustic components, loud calls are regularly accompanied by stereotyped motoric displays. The motoric and acoustic components of loud call displays appear independently of each other and at different times during ontogeny. The development of the display is characterized by combination of units with different structural features and synchronization of vocal and motoric components. Although more evidence is needed, our observations suggest that the development of loud call displays coincides with the aquisitation of social maturation and competence and requires not only social experience but also a certain amount of motoric training. In spite of the high degree of ritualization, loud call displays are not completely fixed in form, but instead are open to individual- and population-specific variation.