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Demography and reproductive output in langurs of the Western Ghats, India

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Abstract

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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References

  • Altmann J, Alberts SC (2005) Growth rates in a wild primate population: ecological influences and maternal effects. Behav Ecol Sociobiol 57:490–501

    Article  Google Scholar 

  • Ashalakshmi NC, Chetan Nag KS, Karanth KP (2015) Molecules support morphology: species status of south Indian populations of the widely distributed Hanuman langur. Conserv Genet 16:43–58

    Article  CAS  Google Scholar 

  • Böhning-Gaese K, Oberrath R (1999) Phylogenetic effects on morphological, life-history, behavioural and ecological traits of birds. Evol Ecol Res 1:347–364

    Google Scholar 

  • Borries C, Koenig A, Winkler P (2001) Variation of life history traits and mating patterns in female langur monkeys (Semnopithecus entellus). Behav Ecol Sociobiol 50:391–402

    Article  Google Scholar 

  • Borries C, Larney E, Lu A, Ossi K, Koenig A (2008) Costs of group size: lower developmental and reproductive rates in larger groups of leaf monkeys. Behav Ecol 19:1186–1191

    Article  Google Scholar 

  • Borries C, Lu A, Ossi-Lupo K, Larney E, Koenig A (2011) Primate life histories and dietary adaptations: a comparison of Asian colobines and macaques. Am J Phys Anthropol 144:286–299

    Article  PubMed  Google Scholar 

  • Chapman CA, Rothman JM (2009) Within-species differences in primate social structure: evolution of plasticity and phylogenetic constraints. Primates 50:12–22

    Article  PubMed  Google Scholar 

  • Charnov EL, Berrigan D (1993) Why do female primates have such long life spans and so few babies? Or life in the slow lane. Evol Anthropol 1:191–194

    Article  Google Scholar 

  • Chhangani AK (2002) Group composition and sex ratio in Hanuman langurs (Semnopithecus entellus) in the Aravali Hills of Rajasthan, India. Zoo’s Print J 17:848–852

    Article  Google Scholar 

  • Cords M, Chowdhury S (2010) Life history of Cercopithecus mitis stuhlmanni in the Kakamega Forest, Kenya. Int J Primatol 31:433–455

    Article  Google Scholar 

  • Deaner RO, Barton RA, van Schaik CP (2003) Primate brains and life histories: renewing the connection. In: Kappeler PM, Pereira ME (eds) Primate life histories and socioecology. Cambridge University Press, Cambridge, pp 233–265

    Google Scholar 

  • Dunbar RIM (1987) Demography and reproduction. In: Smuts BB, Cheney DL, Seyfarth RM, Wrangham RW, Struhsaker TT (eds) Primate societies. University of Chicago Press, Chicago, pp 240–249

    Google Scholar 

  • Fleagle JG (1999) Primate adaptation and evolution. Academic Press, San Diego

    Google Scholar 

  • Gadgil M, Bossert WH (1970) Life historical consequences of natural selection. Am Nat 104:1–24

    Article  Google Scholar 

  • Gilmore D, Cook B (1981) Environmental factors in mammal reproduction. MacMillan, London

    Book  Google Scholar 

  • Harris TR (2006) Between-group contest competition for food in a highly folivorous population of black and white colobus monkeys (Colobus guereza). Behav Ecol Sociobiol 61:317–329

    Article  Google Scholar 

  • Hilgartner R, Zinner D, Kappeler PM (2008) Life history traits and parental care in Lepilemur ruficaudatus. Am J Primatol 70:2–11

    Article  PubMed  Google Scholar 

  • Isbell LA, Young TP, Jaffe KE, Carlson AA, Chancellor RL (2009). Demography and life histories of sympatric patas monkeys, Erythrocebus patas, and vervets, Cercopithecus aethiops, in Laikipia, Kenya. Int J Primatol 30:103–124

    Article  PubMed  PubMed Central  Google Scholar 

  • Janson CH, Goldsmith ML (1995) Predicting group size in primates: foraging costs and predation risks. Behav Ecol 6:326–336

    Article  Google Scholar 

  • Kamilar JM, Cooper N (2013) Phylogenetic signal in primate behaviour, ecology and life history. Philos Trans R Soc B 368(1618):20120341

    Article  Google Scholar 

  • Kavana TS, Erinjery JJ, Singh M (2015a) Folivory as a constraint on social behaviour of langurs in south India. Folia Primatol 86:420–431

    Article  PubMed  Google Scholar 

  • Kavana TS, Erinjery JJ, Singh M (2015b) Diet of Nilgiri langur Semnopithecus johnii inhabiting tropical montane shola in the Nilgiri hills, south India. Asian Primates J. 5:3–11

    Google Scholar 

  • Koenig A (2000) Competitive regimes in forest-dwelling Hanuman langur females (Semnopithecus entellus). Behav Ecol Sociobiol 48:93–109

    Article  Google Scholar 

  • Koenig A, Beise J, Chalise MK, Ganzhorn JU (1998) When females should contest for food–testing hypotheses about resource density, distribution, size, and quality with Hanuman langurs (Presbytis entellus). Behav Ecol Sociobiol 42:225–237

    Article  Google Scholar 

  • Korstjens AH, Lehmann J, Dunbar RIM (2010) Resting time as an ecological constraint on primate biogeography. Anim Behav 79:361–374

    Article  Google Scholar 

  • Lee PC (1987) Nutrition, fertility and maternal investment in primates. J Zool 213:409–422

    Article  Google Scholar 

  • Lehmann J, Korstjens AH, Dunbar RIM (2007) Group size, grooming and social cohesion in primates. Anim Behav 74:1617–1629

    Article  Google Scholar 

  • Leigh SR (1994) Ontogenetic correlates of diet in anthropoid primates. Am J Phys Anthropol 94:499–522

    Article  CAS  PubMed  Google Scholar 

  • Martin RD (1990) Primate origins and evolution: a phylogenetic reconstruction. Princeton University Press, Princeton

    Google Scholar 

  • Moore J (1999) Population density, social pathology, and behavioral ecology. Primates 40:1–22

    Article  CAS  PubMed  Google Scholar 

  • Nishida T, Corp N, Hamai M, Hasegawa T, Hiraiwa-Hasegawa M, Hosaka K et al (2003) Demography, female life history, and reproductive profiles among the chimpanzees of Mahale. Am J Primatol 59:99–121

    Article  PubMed  Google Scholar 

  • Raichlen DA, Gordon AD, Muchlinski M, Snodgrass JJ (2010) Causes and significance of variation in mammalian basal metabolism. J Comp Physiol B 180:301–311

    Article  PubMed  Google Scholar 

  • Rajpurohit LS, Sommer V (1991) Sex differences in mortality among langurs (Presbytis entellus) of Jodhpur, Rajasthan. Folia Primatol 56:17–27

    Article  Google Scholar 

  • Robbins MM, Bermejo M, Cipolletta C, Magliocca F, Parnell RJ, Stokes E (2004) Social structure and life-history patterns in western gorillas (Gorilla gorilla gorilla). Am J Primatol 64:145–159

    Article  PubMed  Google Scholar 

  • Ross C (1992a) Environmental correlates of the intrinsic rate of natural increase in primates. Oecologia 90:383–390

    Article  Google Scholar 

  • Ross C (1992b) Basal metabolic rate, body weight and diet in primates: an evaluation of the evidence. Folia Primatol 58:7–23

    Article  CAS  PubMed  Google Scholar 

  • Ross C (1998) Primate life histories. Evol Anthropol 6:54–63

    Article  Google Scholar 

  • Ross C, Jones KE (1999) Socioecology and the evolution of primate reproductive rates. In: Lee PC (ed) Comparative primate socioecology. Cambridge University Press, Cambridge, pp 73–110

    Chapter  Google Scholar 

  • Rowe N (1996) The pictorial guide to the living primates. Pogonias, New York

    Google Scholar 

  • Roy D (2012) Group size and age-sex composition of Nilgiri langur Trachypithecus johnii (Primates: Cercopithecidae) in India. TAPROBANICA: J Asian Biodiv 4:83–87

    Article  Google Scholar 

  • Singh M, Sinha A (2004) Life-history traits: ecological adaptations or phylogenetic relics? In: Theirry B, Singh M, Kaumanns W (eds) Macaque societies: a model for the study of social organization. Cambridge University Press, Cambridge, pp 80–83

    Google Scholar 

  • Snaith TV, Chapman CA (2007) Primate group size and interpreting socioecological models: do folivores really play by different rules? Evol Anthropol 16:94–106

    Article  Google Scholar 

  • Snodgrass JJ, Leonard WR, Robertson ML (2007) Primate bioenergetics: an evolutionary perspective. In: Ravosa MJ, Dagosto M (eds) Primate origins: adaptations and evolution. Springer, New York, pp 703–737

    Chapter  Google Scholar 

  • Stearns SC (1992) The evolution of life histories, vol. 249. Oxford University Press, Oxford

  • Sushma HS, Sunderraj SFW, Johnsingh AJT (2014) The Nilgiri langur. In: Johnsingh AJT, Manjeraker N (eds) Mammals of south Asia, vol 1. Universities Press, Hyderabad, pp 236–254

    Google Scholar 

  • Vasudev D, Kumar A, Sinha A (2008) Resource distribution and group size in the common langur Semnopithecus entellus in southern India. Am J Primatol 70:680–689

    Article  PubMed  Google Scholar 

  • Wich SA, Steenbeek R, Sterck EH, Korstjens AH, Willems EP, Van Schaik CP (2007) Demography and life history of Thomas langurs (Presbytis thomasi). Am J Primatol 69:641–651

    Article  PubMed  Google Scholar 

  • Zucker EL, Clarke MR (2003) Longitudinal assessment of immature-to-adult ratios in two groups of Costa Rican Alouatta palliata. Int J Primatol 24:87–101

    Article  Google Scholar 

Download references

Acknowledgments

We thank the Chief Wildlife Warden and the officials of the Kerala, Tamil Nadu and Karnataka Forest Departments for permission to conduct this study and for their field assistance. We thank Mukesh Chalise and Wolfgang Dittus for comments that enhanced the quality of this article. This study was supported by a Department of Science and Technology Ramanna Fellowship, India to M. S. Our work conformed to the ethical guidelines for animal treatment of the University of Mysore, Mysore, India. Further, our work adhered to all the legal requirements for conducting wildlife research in India. Permits were obtained from the Forest Departments of Kerala, Tamil Nadu and Karnataka for fieldwork.

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Correspondence to Mewa Singh.

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Singh, M., Kumara, H.N., Kavana, T.S. et al. Demography and reproductive output in langurs of the Western Ghats, India. Primates 57, 501–508 (2016). https://doi.org/10.1007/s10329-016-0550-2

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  • DOI: https://doi.org/10.1007/s10329-016-0550-2

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