Abstract
The field of primatology has reached the stage where there are sufficient long-term studies and many shorter investigations on the same species at many different locations, in which we are able to appreciate how variable the behaviour of primates can be and how predictable their environment is over space and time. For example, redtail monkeys (Cercopithecus ascanius) exhibit extreme flexibility in diet; i.e. within the same national park, the amount of time they spend eating fruit varies from 36 to 60% of their foraging time, and among populations, time spent eating fruit ranges from 13 to 61%. Similarly, long-term phenological data from the same area encompassing over two decades illustrate that fruit availability can vary among years by as much as eightfold. While data have steadily accumulated on how variable primate behaviour and proposed environmental predictors of behaviour can be, this information has not been used to effectively re-evaluate theory. For example, current primate socioecological theory has derived general frameworks using the average behavioural traits of species or genera, but these new data suggest it is inappropriate to use such averages. Similarly, environments have often been characterized by single studies of 2 years or less, which does not sufficiently account for environmental variation. Here, we present examples of behavioural and ecological variation and consider ways that our field could advance in the future by considering this variation.
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References
Alberts SC, Altmann J (2012) The Amboseli Baboon Research Project: 40 years of continuity and change. In: Kappeler P, Watts DP (eds) Long-term field studies of primates. Springer, Berlin, pp 261–288
Anderson DP, Nordheim E, Moermond TC, Bi G, Zoro B, Boesch C (2005) Factors Influencing Tree Phenology in Taï National Park, Côte d’Ivoire1. Biotropica 37:631–640
Ashton PS, Givinish T, Appanah S (1988) Staggered flowering in the Dipterocarpaceae: new insights into floral induction and the evolution of mast fruiting in the aseasonal tropics. Am Nat 132:44–66
Bortolamiol S, Cohen M, Potts K, Rwaburindore P, Kasenene J, Seguya A, Pennec F, Viguaud Q, S. K (2014) Suitable habitats for endangered frugivorous mammals: small-scale comparison, regeneration forest and chimpanzee density in Kibale National Park, Uganda. PLoS One 9:e102177
Bush MB (2000) Ecology of a changing planet. Prentice Hall, Upper Saddle River
Butynski TM (1990) Comparative ecology of blue monkeys (Cercopithecus mitis) in high- and low-density sub-populations. Ecol Monogr 60:1–26
Campos FA, Morris WF, Alberts SC, Altmann J, Brockman DK, Cords M, Pusey A, Stoinski TS, Strier KB, Fedigan LM (2017) Does climate variability influence the demography of wild primates? Evidence from long-term life-history data in seven species. Glob Chang Biol
Chapman CA (1990) Ecological constraints on group size in three species of neotropical primates. Folia Primatol 55:1–9
Chapman CA, Fedigan LM (1990) Dietary differences between neighboring cebus monkey groups: local traditions or responses to food availability? Folia Primatol 54:177–186
Chapman CA, Peres CA (2001) Primate conservation in the new millennium: the role of scientists. Evol Anthropol 10:16–33
Chapman CA, Rothman JM (2009) Within-species differences in primate social structure: evolution of plasticity and phylogenetic constraints. Primates 50:12–22
Chapman CA, Chapman LJ, Wrangham RW, Hunt K, Gebo D, Gardner L (1992) Estimators of fruit abundance of tropical trees. Biotropica 24:527–531
Chapman CA, Wrangham RW, Chapman LJ (1994) Indices of habitat-wide fruit abundance in tropical forest. Biotropica 26:160–171
Chapman CA, Wrangham RW, Chapman LJ (1995) Ecological constraints on group size: an analysis of spider monkey and chimpanzee subgroups. Behavioural Ecology and Sociobiology 36:59–70
Chapman CA, Chapman LJ, Cords M, Gauthua M, Gautier-Hion A, Lambert JE, Rode KD, Tutin CEG, White LJT (2002a) Variation in the diets of Cercopithecus species: differences within forests, among forests, and across species. In: Glenn M, Cords M (eds) The guenons: diversity and adaptation in African monkeys. Plenum, New York, pp 319–344
Chapman CA, Chapman LJ, Gillespie TR (2002b) Scale issues in the study of primate foraging: red colobus of Kibale National Park. Am J Phys Anthropol 117:349–363
Chapman CA, Chapman LJ, Naughton-Treves L, Lawes MJ, McDowell LR (2004) Predicting folivorous primate abundance: validation of a nutritional model. Am J Primatol 62:55–69
Chapman CA, Chapman LJ, Zanne AE, Poulsen JR, Clark CJ (2005a) A 12-year phenological record of fruiting: implications for frugivore populations and indicators of climate change. In: Dew JL, Boubli JP (eds) Tropical fruits and frugivores. Springer, The Netherlands, pp 75–92
Chapman CA, Struhsaker TT, Lambert JE (2005b) Thirty years of research in Kibale National Park, Uganda, reveals a complex picture for conservation. Int J Primatol 26:539–555
Chapman CA, Corriveau A, Schoof VAM, Twinomugisha D, Valenta K (2017) Long-term primate research and its significance for developing theory and conservation plans. J Mammal 98:652–660
Chapman CA, Valenta K, Bonnell TR, Brown KA, Chapman LJ (in press) Solar radiation drives fruit phenology: Evaluating a 16 year record from Kibale National Park, Uganda. Proceedings of the Royal Society of London B: Biological Sciences
Clutton-Brock TH, Harvey PH (1977) Primate ecology and social organization. Journal of Zoological Society of London 183:1–39
Clutton-Brock T, Janson C (2012) Primate socioecology at the crossroads: past, present, and future. Evolutionary Anthropology: Issues, News, and Reviews 21:136–150
Colwell RK (1974) Predictability, constancy, and contingency of periodic phenomena. Ecology 55:1148–1153
Croat TB (1978) Flora of Barro Colorado Island. Stanford University Press, Stanford
Davies SJ, Ashton PS (1999) Phenology and fecundity in 11 sympatric pioneer species of Macaranga (Euphorbiaceae) in Borneo. Am J Bot 86:1786–1795
Davies AG, Oates JF, Dasilva GL (1999) Patterns of frugivory in three West African colobine monkeys. Int J Primatol 20:327–357
Dewar RE, Richard AF (2007) Evolution in the hypervariable environment of Madagascar. Proc Natl Acad Sci 104:13723–13727
Dunbar RIM (2003) The social brain: mind, language, and society in evolutionary perspective. Annu Rev Anthropol 32:163–181
Dunham AE (2008) Battle of the sexes: cost asymmetry explains female dominance in lemurs. Anim Behav 76:1435–1439
Eisenberg JF, Muckenhirn NA, Rudran R (1972) The relation between ecology and social structure in primates. Science 176:863–874
Federman S, Sinnott-Armstrong M, Baden AL, Chapman CA, Daly DC, Richard AR, Valenta K, Donoghue MJ (2017) The paucity of frugivores in Madagascar may not be due to unpredictable temperatures or fruit resources. PLoS One 12:e0168943
Fedigan LM, Jack KM (2012) Tracking neotropical monkeys in Santa Rosa: lessons from a regenerating Costa Rican dry forest. In: Kappeler P, Watts D (eds) Long-term field studies of primates. Springer, Heidelberg, pp 165–184
Frankie GW, Baker HG, Opler PA (1974) Comparative phenological studies of trees in tropical wet and dry forests in the lowlands of Costa Rica. J Ecol 62:881–919
Gautier-Hion A, Michaloud G (1989) Are figs always keystone resources for tropical frugivorous vertebrates? A test in Gabon. Ecology 70:1826–1833
Gogarten JF, Jacob AL, Ghai RR, Rothman JM, Twinomugisha D, Wasserman MD, Chapman CA (2015) Group size dynamics over 15+ years in an African forest primate community. Biotropica 47:101–112
Hogan J, Melin A (2018, this volume) Intra- and interannual variation in the fruit diet of wild capuchins: impact of plant phenology. In: Kalbitzer U, Jack KM (eds) Primate life histories, sex roles, and adaptability – essays in Honour of Linda M Fedigan developments in primatology: progress and prospects. Springer, New York, pp 193–210
Isbell LA (1991) Contest and scramble competition: patterns of female aggression and ranging behaviour among primates. Behav Ecol 2:143–155
Janson CH (1983) Adaptation of fruit morphology to dispersal agents in a neotropical rainforest. Science 219:187–189
Janson CH (2000) Primate socio-ecology: the end of a golden age. Evol Anthropol 9:73–86
Janson CH, Chapman CA (1999) Resources and the determination of primate community structure. In: Fleagle JG, Janson CH, Reed KE (eds) Primate Communities. Cambridge University Press, Cambridge, pp 237–267
Janson CH, van Schaik CP (1988) Recognizing the many faces of primate food competition: methods. Behaviour 105:165–186
Janzen DH (1967) Synchronization of sexual reproduction of trees within a dry season in Central America. Evolution 21:620–637
Kappeler PM, Fichtel C (2015) Eco-evo-devo of the lemur syndrome: did adaptive behavioral plasticity get canalized in a large primate radiation? Front Zool 12:S15
Kappeler PM, Watts DP (2012) Long-term field studies of primates. Springer, Berlin
Koenig A (2002) Competition for resources and its behavioral consequences among female primates. Int J Primatol 23:759–783
Koenig A, Borries C (2006) The predictive power of socioecological models: a reconsideration of resource characteristics, agonism and dominance hierarchies. In: Hohmann G, Robbins MM, Boesch C (eds) Feeding ecology in apes and other primates. Cambridge University Press, Cambridge, pp 263–284
Lambert JE (2009) Primate fallback strategies as adaptive phenotypic plasticity: scale, process, and pattern. Am J Phys Anthropol 140:759–766
Langergraber KE, Prüfer K, Rowney C, Boesch C, Crockford C, Fawcett K, Inoue E, Inoue-Muruyama M, Mitani JC, Muller MN (2012) Generation times in wild chimpanzees and gorillas suggest earlier divergence times in great ape and human evolution. Proc Natl Acad Sci 109:15716–15721
Leigh SR (1994) Ontoaenetic correlates of diet in anthropoid primates. Am J Phys Anthropol 94:499–522
Marshall AJ, Boyko CM, Feilen KL, Boyko RH, Leighton M (2009) Defining fallback foods and assessing their importance in primate ecology and evolution. Am J Phys Anthropol, in press
McNab BK (2002) The physiological ecology of vertebrates: a view from energetics. Cornell University Press, Cornell
Melin AD, Young HC, Mosdossy KN, Fedigan LM (2014) Seasonality, extractive foraging and the evolution of primate sensorimotor intelligence. J Hum Evol 71:77–86
Mosdossy KN, Melin AD, Fedigan LM (2015) Quantifying seasonal fallback on invertebrates, pith, and bromeliad leaves by white-faced capuchin monkeys (Cebus capucinus) in a tropical dry forest. Am J Phys Anthropol 158:67–77
Newbery DM, Songwe NC, Chuyong GB (1998) Phenology and dynamics of an African rainforest at Korup, Cameroon. In: Newbery DM, Pins HHT, Brown ND (eds) Dynamics of tropical communities. Blackwell, Oxford
Oates JF, Whitesides GH, Davies AG, Waterman PG, S.M. G, DaSilva GL, Mole S (1990) Determinants of variation in tropical forest primate biomass: new evidence from West Africa. Ecology 71:328–343
Opler PA, Frankie GW, Baker HG (1976) Rainfall as a factor in the release, timing, and synchronization of anthesis by tropical trees and shrubs. J Biogeogr 3:231–236
Overdorff DJ (1996a) Ecological correlates to activity and habitat use of two prosimian primates: Eulemur rubriventer and Eulemur fulvus rufus in Madagascar. Am J Primatol 40:327–342
Overdorff DJ (1996b) Ecological correlates to social structure in two lemur species in Madagascar. Am J Phys Anthropol 100:487–506
Pau S, Wolkovich EM, Cook BI, Davies TJ, Kraft NJB, Bolmgren K, Betancourt JL, Cleland EE (2011) Predicting phenology by integrating ecology, evolution, and climate science. Glob Chang Biol 17:3633–3646
Peres CA (2000) Identifying keystone plant resources in tropical forests: the case of gums from Parkia pods. J Trop Ecol 16:287–317
Pochron ST, Fitzgerald J, Gilbert CC, Lawrence D, Grgas M, Rakotonirina G, Ratsimbazafy R, Rakotosoa R, Wright PC (2003) Patterns of female dominance in Propithecus diadema edwardsi of Ranomafana National Park, Madagascar. Am J Primatol 61:173–185
Polansky L, Boesch C (2013) Long-term changes in fruit phenology in a West African lowland tropical rain forest are not explained by rainfall. Biotropica 45:434–440
Power ME, Tilman D, Estes JA, Menge BA, Bond WJ, Mills LS, Daily G, Castilla JC, Lubchenco J, Paine RT (1996) Challenges in the quest for keystones. Bioscience 46:609–620
Rathke B, Lacey EP (1985) Phenological patterns of terrestrial plants. Annu Rev Ecol Syst 16:179–214
Rode KD, Chapman CA, Chapman LJ, McDowell LR (2003) Mineral resource availability and consumption by colobus in Kibale National Park, Uganda. Int J Primatol 24:541–573
Rothman JM, Raubenheimer D, Chapman CA (2011) Nutritional geometry: gorillas prioritize non-protein energy while consuming surplus protein. Biol Lett:rsbl20110321
Rothman JM, Chapman CA, van Soest PJ (2012) Methods in primate nutritional ecology: a user’s guide. Int J Primatol 33:542–566
Smythe N (1970) Relationships between fruiting seasons and seed dispersal methods in a neotropical forest. Am Nat 104:25–35
Snaith TV, Chapman CA (2007) Primate group size and socioecological models: do folivores really play by different rules? Evol Anthropol 16:94–106
Snaith TV, Chapman CA (2008) Red colobus monkeys display alternative behavioural responses to the costs of scramble competition. Behav Ecol 19:1289–1296
Snow DW (1965) A possible selective factor in the evolution of fruiting seasons in tropical forests. Oikos 15:274–281
Sterck EHM, Watts DP, van Schaik CP (1997) The evolution of female social relationships in nonhuman primates. Behav Ecol Sociobiol 41:291–309
Teaford MF, Walker A (1984) Quantitative differences in dental microwear between primate species with different diets and a comment on the presumed diet of Sivapithecus. Am J Phys Anthropol 64:191–200
Terborgh J (1983) Five new world primates. Princeton University Press, Princeton
Terborgh J (1986) Keystone plant resources in the tropical forest. In: Soule ME (ed) Conservation biology: the science of scarcity and diversity. Sinauer, Sunderland, pp 330–344
Twinomugisha D, Chapman CA (2008) Golden monkey ranging in relation to spatial and temporal variation in food availability. Afr J Ecol 46:585–593
van Schaik CP (1983) Why are diurnal primates living in groups? Behaviour 87:120–144
van Schaik CP (1989) The ecology of social relationships amongst female primates. In: Standen V, Foley RA (eds) Comparative socioecology: the behavioural ecology of humans and other mammals. Blackwell Scientific Publications, Boston, pp 195–218
van Schaik CP, Terborgh JW, Wright SJ (1993) The phenology of tropical forests: adaptive significance and consequences for primary consumers. Annu Rev Ecol Syst 24:353–377
Visser MD, Jongejans E, van Breugelm N, Zuidema PA, Chen Y-Y, Kassim AR, de Kroon H (2011) Strict mast fruiting for a tropical dipterocarp tree: a demographic cost-benefit analysis of delayed reproduction and seed predation. J Ecol 99:1033–1044
Wheelwright NT (1985) Fruit size, gape width, and the diets of fruit-eating birds. Ecology 66:808–818
Wrangham RW (1979) On the evolution of ape social systems. Soc Sci Inf 18:335–368
Wrangham RW (1980) An ecological model of female-bonded primate groups. Behaviour 75:262–300
Wright PC (1999) Lemur traits and Madagascar ecology: coping with an island environment. Yearb Phys Anthropol 43:31–72
Wright S, Calderón O (2006) Seasonal, El Nino and longer term changes in flower and seed production in a moist tropical forest. Ecol Lett 9:35–44
Acknowledgements
This paper is dedicated to Dr. Linda Fedigan who was so very influential to Colin Chapman starting his research career when he was an undergrad, supervised him through his graduate degrees, and then has provided critical mentorship and letters of recommendation to this day. Funding for the research in Kibale National Park was provided by the Canada Research Chairs Program, Natural Science and Engineering Research Council of Canada, Fonds Québécois de la Recherché sur la Nature et les Technologies, and the National Geographic Society. Tom Struhsaker has been particularly helpful over the years with sharing long-term data and opinions, and Karen Strier provided stimulating ideas and discussion on variability and flexibility. Finally, we would like to thank Urs Kalbitzer, Kathy Jack, and the anonymous reviewers for helpful comments on the manuscript.
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Chapman, C.A., Valenta, K., Bortolamiol, S. (2018). How Variable Is a Primate’s World: Spatial and Temporal Variation in Potential Ecological Drivers of Behaviour?. In: Kalbitzer, U., Jack, K. (eds) Primate Life Histories, Sex Roles, and Adaptability. Developments in Primatology: Progress and Prospects. Springer, Cham. https://doi.org/10.1007/978-3-319-98285-4_17
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