Mechanical and Nutritional Properties of Food as Factors in Platyrrhine Dietary Adaptations

  • Marilyn A. Norconk
  • Barth W. Wright
  • Nancy L. Conklin-Brittain
  • Christopher J. Vinyard
Part of the Developments in Primatology: Progress and Prospects book series (DIPR)


Spider Monkey Fruit Pulp Nutritional Property Bite Force Total Nonstructural Carbohydrate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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  1. Agrawal, K. R., Lucas, P. W., Prinz, J. F., and Bruce, I. C. 1997. Mechanical properties of foods responsible for resisting food breakdown in the human mouth. Arch. Oral Biol. 42:1–9.PubMedCrossRefGoogle Scholar
  2. Agrawal, K. R., Lucas, P. W., Bruce, I. C., and Prinz, J. F. 1998. Food properties that influence neuromuscular activity during human mastication. J. Dent. Res. 77:1931–1938.PubMedCrossRefGoogle Scholar
  3. Aguiar, J. P. L., Marinho, H. A., Rebelo, Y. S., and Shrimpton, R. 1980. Aspectos nutritivos de alguns frutos da Amazônia. Acta Amazonica 10:755–758.Google Scholar
  4. Altmann, S. A. 1998. Foraging for Survival: Yearling Baboons in Africa. Chicago: University of Chicago Press.Google Scholar
  5. Anapol, F., and Lee, S. 1994. Morphological adaptations to diet in platyrrhine primates. Am. J. Phys. Anthropol. 94:239–261.PubMedCrossRefGoogle Scholar
  6. Anthony, M. R. L., and Kay, R. F. 1993. Tooth form and diet in Ateline and Alouattine primates: reflections on the comparative method. Am. J. Sci. 293-A:356–382.Google Scholar
  7. Ayres, J. M. 1986. Uakaris and Amazonian Flooded Forest. PhD Dissertation. University of Cambridge.Google Scholar
  8. Ayres, J. M. 1989. Comparative feeding ecology of the Uakari and Bearded Saki, Cacajao and Chiropotes. J. Hum. Evol. 18:697–716.CrossRefGoogle Scholar
  9. Blaxter, K. L. 1989. Energy Metabolism in Animals and Man. New York: Cambridge University Press.Google Scholar
  10. Bouvier, M. 1986a. A biomechanical analysis of mandibular scaling in Old World monkeys. Am. J. Phys. Anthropol. 69:473–482.CrossRefGoogle Scholar
  11. Bouvier, M. 1986b. Biomechanical scaling of mandibular dimension in New World Monkeys. Int. J. Primatol. 7:551–567.CrossRefGoogle Scholar
  12. Bouvier, M., and Tsang, S. M. 1990. Comparison of muscle weight and force ratios in New and Old World monkeys. Am. J. Phys. Anthropol. 82:509–515.PubMedCrossRefGoogle Scholar
  13. Brown, A. D., and Zunino, G. E. 1990. Dietary variability in Cebus apella in extreme habitats: evidence for adaptability. Folia Primatol. 54:187–195.PubMedCrossRefGoogle Scholar
  14. Cachel, S. M. 1979. A functional analysis of the primate masticatory system and the origin of the anthropoid post-orbital septum. Am. J. Phys. Anthropol. 50:1–18.CrossRefGoogle Scholar
  15. Castellanos, H. G., and Chanin, P. 1996. Seasonal differences in food choice and patch preference of long-haired spider monkeys (Ateles belzebuth). In M. A. Norconk, A. L. Rosenberger and P. A. Garber (eds.), Adaptive Radiations of Neotropical Primates (pp. 451–466). New York: Plenum.Google Scholar
  16. Chapman, C. A., and Chapman, L. J. 1991. The foraging itinerary of spider monkeys: when to eat leaves? Folia Primatol. 56:162–166.CrossRefGoogle Scholar
  17. Chapman, C. A., Chapman, L. J., Rode, K. D., Hauck, E. M., and McDowell, L. R. 2003. Variation in the nutritional value of primate foods: among trees, time periods, and areas. Int. J. Primatol. 24:317–333.CrossRefGoogle Scholar
  18. Chew, C. L., Lucas, P. W., Tay, D. K. L., Keng, S. B., and Ow, R. K. K. 1988. The effect of food texture on the replication of jaw movements in mastication. J. Dent. 16:210–214.PubMedCrossRefGoogle Scholar
  19. Chivers, D. J., and Hladik, C. M. 1980. Morphology of the gastrointestinal tract in primates: comparisons with other mammals in relation to diet. J. Morphol. 166:337–386.PubMedCrossRefGoogle Scholar
  20. Coimbra-Filho, A. F., and Mittermeier, R. A. 1977. Tree-gouging, exudate-eating and the “short tusked” condition in Callithrix and Cebuella. In D. G. Kleiman (ed.), The Biology and Conservation of the Callitrichidae (pp. 105–115). Washington DC: Smithsonian InstitutionPress.Google Scholar
  21. Cole, T. M. 1992. Postnatal heterochrony of the masticatory apparatus in Cebus apella and Cebus albifrons. J. Hum. Evol. 23:253–282.CrossRefGoogle Scholar
  22. Conklin-Brittain, N. L., Wrangham, R. W., and Hunt, K. D. 1998. Dietary response of chimpanzees and cercopithecines to seasonal variation in fruit abundance. II. Macronutrients. Int. J. Primatol 19:971–998.CrossRefGoogle Scholar
  23. Conklin-Brittain, N. L., Knott, C. D., and Wrangham, R. W. 2006. Energy intake by wild chimpanzees and orangutans: methodological considerations and a preliminary comparison. In G. Hohmann, M. M. Robbins and C. Boesch (eds.), Feeding ecology in apes and other primates: ecological, physical and behavioral aspects (pp. 445–471). New York: Cambridge University Press.Google Scholar
  24. Covert, H. H. 1986. Biology of early Cenozoic primates. In D. R. Swindler and J. Erwin (eds.), Comparative Primate Biology, Systematics, Evolution, and Anatomy (pp. 335–359). New York: Alan R. Liss.Google Scholar
  25. Daegling, D. J. 1992. Mandibular morphology and diet in the genus Cebus. Int. J. Primatol. 13:545–570.CrossRefGoogle Scholar
  26. Darvell, B. W., Lee, P. K. D., Yuen, T. D. B., and Lucas, P. W. 1996. A portable fracture toughness tester for biological materials. Meas. Sci. Tech. 7:954–962.CrossRefGoogle Scholar
  27. Deagling, D. J. 2007. Morphometric estimation of torsional stiffness and strength in primate mandibles. Am. J. Phys. Anthropol. 132:261–266.CrossRefGoogle Scholar
  28. Di Fiore, A. 2004. Diet and feeding ecology of woolly monkeys in a western Amazonian rain forest. Int. J. Primatol. 25:767–801.CrossRefGoogle Scholar
  29. Di Fiore, A., and Campbell, C. J. 2007. The Atelines: Variation in ecology, behavior, and social organization. In C. J. Campbell, A. Fuentes, K. C. MacKinnon, M. Panger and S. K. Bearder (eds.), Primates in Perspective (pp. 155–185). Oxford UK: Oxford University Press.Google Scholar
  30. Eaglen, R. H. 1984. Incisor size and diet revisited: The view from a platyrrhine perspective. Am. J. Phys. Anthropol. 64:263–275.PubMedCrossRefGoogle Scholar
  31. Eaglen, R. H. 1986. Morphometrics of the anterior dentition in strepsirhine primates. Am. J. Phys. Anthropol. 71:185–201.PubMedCrossRefGoogle Scholar
  32. Edwards, M. S., and Ullrey, D. E. 1999. Effect of dietary fiber concentration on apparent digestibility and digesta passage in non-human primates. II. Hindgut and forgut fermenting folivores. Zoo Biol. 18:537–549.Google Scholar
  33. Emery-Thompson, E., Kahlenberg, S. M., Gilby, I. C., and Wrangham, R. W. 2007. Core area quality is associated with variance in reproductive success among female chimpanzees at Kibale National Park. Anim. Behav. 73:501-512.CrossRefGoogle Scholar
  34. Fernandez-Duque, E. 2007. Aotinae: social monogamy in the only nocturnal haplorrhines. In C. J. Campbell, A. Fuentes, K. C. MacKinnon, M. Panger and S. K. Bearder (eds.), Primates in Perspective (pp. 139–154). Oxford UK: Oxford University Press.Google Scholar
  35. Fleagle, J. G., and Tejedor, M. F. 2002. Early platyrrhines of southern South America. In W. C. Hartwig (ed.), The Primate Fossil Record (pp. 161–173). Cambridge UK: Cambridge University Press.Google Scholar
  36. Foley, W. J., and Cork, S. J. 1992. Use of fibrous diets by small herbivores: How far can the rules be “bent”? Trends Ecol. Evol. 7:159–162.Google Scholar
  37. Forget, P.-M. 1991. Comparative recruitment pattern of two non-pioneer tree species in French Guiana. Oecologia 85:434–439.CrossRefGoogle Scholar
  38. Fragaszy, D. M. 1986. Time budgets and foraging behaviors in wedge-capped capuchins (Cebus olivaceus): age and sex differences. In D. Taub and F. King (eds.), Current Perspectives in Primate Social Dynamics (pp. 159–174). New York: Van Nostrand Press.Google Scholar
  39. Garber, P. A. 1988. Foraging decisions during nectar feeding by tamarin monkeys (Saguinus mystax and Saguinus fuscicollis, Callitrichidae, Primates) in Amazonian Peru. Biotropica 20:100–106.CrossRefGoogle Scholar
  40. Garber, P. A. 1992. Vertical clinging, small body size, and the evolution of feeding adaptations in the Callitrichinae. Am. J. Phys. Anthropol. 88:469–482.PubMedCrossRefGoogle Scholar
  41. Garber, P. A. 1993. Feeding ecology and behavior of the genus Saguinus. In A. B. Rylands (ed.), Marmosets and Tamarins: Systematics, Behavior, and Ecology (pp. 273–295). Oxford UK: Oxford University Press.Google Scholar
  42. Gaulin, S. J. C., and Craker, L. E. 1979. Protein in vegetation and reproductive tissues of several Neotropical species. J. Agri. Food Chem. 27:791–795.CrossRefGoogle Scholar
  43. Greenfield, L. O. 1992. Relative canine size, behavior and diet in male ceboids. J. Hum. Evol. 23:469–80.CrossRefGoogle Scholar
  44. Guimarães Jr., P. R., José, J., Galetti, M., and Trigo, J. R. 2003. Quinolizidine alkaloids in Ormosia arborea seeds inhibit predation but not hoarding by agoutis (Dasyprocta leporina). J. Chem. Ecol. 29:1065–1072.PubMedCrossRefGoogle Scholar
  45. Hanson, A. M., Hall, M. B., Porter, L., and Lintzenich, B. 2006. Composition and nutritional characteristics of fungi consumed by Callimico goeldii in Pando, Bolivia. Int. J. Primatol. 27:323–346.CrossRefGoogle Scholar
  46. Hemingway, C. 1998. Selectivity and variability in the diet of Milne-Edwards’ sifakas (Propithecus diadema edwardsi): Implications for folivory and seed-eating. Int. J. Primatol. 19:355–377.CrossRefGoogle Scholar
  47. Hershkovitz, P. 1977. Living New World Monkeys (Platyrrhini). Chicago: University of Chicago Press.Google Scholar
  48. Heymann, E. W., and Smith, A. C. 1999. When to feed on gums: temporal patterns of gummivory in wild tamarins, Saguinus mystax and Saguinus fuscicollis (Callitrichinae). Zoo. Biol:18:459–471.CrossRefGoogle Scholar
  49. Hiiemae, K. M. 1978. Mammalian mastication: A review of the activity of the jaw muscles and the movements they produce in chewing. In P. M. Butler and K. A. Joysey (eds.), Development, Function and Evolution of Teeth (pp. 361–398). London: Academic Press.Google Scholar
  50. Hiiemae, K. M. 2000. Feeding in mammals. In K. Schwenk (ed.), Feeding (pp. 411–448). New York: Academic Press.CrossRefGoogle Scholar
  51. Hiiemae, K. M., and Crompton, A. W. 1985. Mastication, food transport, and swallowing. In M. Hildebrand, D. B. Bramble, K. Liem and D. Wake (eds.), Functional Vertebrate Morphology (pp. 262–290). Cambridge: Harvard University Press.Google Scholar
  52. Hiiemae K. M., and Kay R. F. 1973. Evolutionary trends in the dynamics of primate mastication. In M. R. Zingeser (ed.), Craniofacial Biology of Primates, Vol. 3: Symp. Fourth Int. Cong. Primatology, (pp. 28–64). Basel: S. Karger.Google Scholar
  53. Hill, D. A., and Lucas P. W. 1996. Toughness and fiber content of major leaf foods of wild Japanese macaques (Macaca fuscata yakui) in Yaushima. Am. J. Primatol. 38:221–231.CrossRefGoogle Scholar
  54. Hladik, C. M., Hladik, A., Bousset, J., Valdebouze, P., Viroben, G., and Delort-Laval, J. 1971. Le regime alimentaire des primates de L’île de Barro-Colorado (Panama). La Terre et la Vie. 1:25–117.Google Scholar
  55. Howe, H. F., and Vande Kerckhove, G. A. 1981. Removal of wild nutmeg (Virola surinamensis) crops by birds. Ecol. 62:1093–1106.CrossRefGoogle Scholar
  56. Hylander, W. L. 1975. The human mandible: Lever or link? Am. J. Phys. Anthropol. 43:227–242.CrossRefGoogle Scholar
  57. Hylander, W. L. 1979a. The functional significance of primate mandibular form. J. Morphol. 160:223–240.CrossRefGoogle Scholar
  58. Hylander, W. L. 1979b. Mandibular function in Galago crassicaudatus and Macaca fascicularis: An in vivo approach to stress analysis of the mandible. J. Morphol. 159:253–296.CrossRefGoogle Scholar
  59. Hylander, W. L. 1984. Stress and strain in the mandibular symphysis of primates: A test of competing hypotheses. Am. J. Phys. Anthropol. 61:1–46.CrossRefGoogle Scholar
  60. Hylander, W. L. 1985. Mandibular function and biomechanical stress and scaling. Am. Zool. 25: 315–330.Google Scholar
  61. Hylander, W. L., Johnson, K. R., and Crompton, A. W. 1987. Loading patterns and jaw movements during mastication in Macaca fascicularis: A bone-strain, electromyographic, and cineradiographic analysis. Am. J. Phys. Anthropol. 72:287–314.PubMedCrossRefGoogle Scholar
  62. Hylander, W. L., Ravosa, M. J., Ross, C. F., and Johnson, K. R. 1998. Mandibular corpus strain in primates: Further evidence for a functional link between symphyseal fusion and jaw-adductor muscle force. Am. J. Phys. Anthropol. 107:257–271.PubMedCrossRefGoogle Scholar
  63. Hylander, W. L., Ravosa, M. J., Ross, C. F., Wall, C. E., and Johnson, K..R 2000. Symphyseal fusion and jaw-adductor muscle force: an EMG study. Am. J. Phys. Anthropol. 112:469–492.PubMedCrossRefGoogle Scholar
  64. Janson, C. 1983. Adaptation of fruit morphology to dispersal agents in a Neotropical forest. Science 219:187–189.PubMedCrossRefGoogle Scholar
  65. Janson, C. H., and Boinski, S. 1992. Morphological and behavioral adaptations for foraging in generalist primates: the case of the cebines. Am. J. Phys. Anthropol. 88:483–498.PubMedCrossRefGoogle Scholar
  66. Kanazawa, E., and Rosenberger, A. L. 1989. Interspecific allometry of the mandible, dental arch, and molar area in anthropoid primates: functional morphology of masticatory components. Primates 30:543–60.CrossRefGoogle Scholar
  67. Kay, R. F. 1975. The functional significance of primate molar teeth. Am. J. Phys. Anthropol. 43:195–215.PubMedCrossRefGoogle Scholar
  68. Kay, R. F. 1977. The evolution of molar occlusion in the Cercopithecidae and early catarrhines. Am. J. Phys. Anthropol. 46:327–352.PubMedCrossRefGoogle Scholar
  69. Kay, R. F. 1984. On the use of anatomical features to infer foraging behavior in extinct primates. In P. S. Rodman and J. G. H. Cant (eds.), Adaptations for Foraging in Nonhuman Primates: Contributions to an Organismal Biology of Prosimians, Monkeys and Apes (pp. 21–53). New York: Columbia University Press.Google Scholar
  70. Kay, R. F., and Covert, H. H. 1984. Anatomy and behavior of extinct primates. In D. J. Chivers, B. A. Wood and A. Bilsborough (eds.), Food Acquisition and Processing in Primates (pp. 467–508). New York: Plenum Press.Google Scholar
  71. Kay, R. F., Johnson, D., and Meldrum, D. J. 1998. A new pitheciin primate from the middle Miocene of Argentina. Am J. Primatol. 45:317–336.PubMedCrossRefGoogle Scholar
  72. Kiltie, R. A. 1982. Bite force as a basis for niche differentiation between rain forest peccaries (Tayassu tajacu and T. pecari). Biotropica 14:188–195.CrossRefGoogle Scholar
  73. Kinzey, W. G. 1974. Ceboid models for the evolution of hominoid dentition. J. Hum. Evol. 3:193–203.CrossRefGoogle Scholar
  74. Kinzey, W. G. 1992. Dietary and dental adaptations in the Pitheciinae. Am. J. Phys. Anthropol. 88:499–514.PubMedCrossRefGoogle Scholar
  75. Kinzey, W. G. 1997. New World Primates: Ecology, Evolution and Behavior. New York: Aldine de Gruyter, Inc.Google Scholar
  76. Kinzey, W. G., and Norconk, M. A. 1990. Hardness as a basis of fruit choice in two sympatric primates. Am. J. Phys. Anthropol. 81:5–15.PubMedCrossRefGoogle Scholar
  77. Kinzey, W. G., and Norconk, M. A. 1993. Physical and chemical properties of fruit and seeds eaten by Pithecia and Chiropotes in Surinam and Venezuela. Int. J. Primatol. 14:207–227.CrossRefGoogle Scholar
  78. Kirk, E. C., and Simons, E. L. 2001. Diets of fossil primates from the Fayum Depression of Egypt: a quantitative analysis of molar shearing. J. Hum. Evol. 40:203–229.PubMedCrossRefGoogle Scholar
  79. Kirkpatrick, C. 1998. Ecology and behavior in snub-nosed and douc langurs. In N. G. Jablonski (ed.), Ecology and Behavior in Snub-nosed and Douc Langurs (pp. 155–190). l.Singapore: World Scientific Publishing, Singapore.Google Scholar
  80. Knott, C. 2001. Female reproductive ecology of the apes: implications for human evolution. In P. T. Ellison (ed.), Reproductive Ecology and Human Evolution (pp. 429–463). New York: Aldine de Gruyter.Google Scholar
  81. Knott, D. D. 2005. Energetic responses to food availability in the great apes: implications for hominin evolution. In D. K. Brockman and C. P. van Schaik (eds.), Seasonality in Primates: Studies of Living and Extinct Human and Non-human Primates (pp. 351–378). New York: Cambridge University Press.Google Scholar
  82. Lambert, J. E. 1998. Primate digestion: Interactions among anatomy, physiology, and feeding ecology. Evol. Anthropol. 7:8–20.CrossRefGoogle Scholar
  83. Lucas. P. W. 2004. Dental Functional Morphology: How Teeth Work. Cambridge: Cambridge University Press.Google Scholar
  84. Lucas, P. W., Corlett, R. T., and Luke, D. A. 1986. Postcanine tooth size and diet in anthropoid primates. Z. Morphol. Anthropol. 76:253–276.PubMedGoogle Scholar
  85. Lucas, P.W., Turner, I.M., Dominy, N.J., and Yamashita, N. 2000. Mechanical defenses to herbivory. Ann. Bot. 86:913–920.CrossRefGoogle Scholar
  86. Lucas, P. W., Beta, T., Darvell, B. W., Dominy, N. J., Essackjee, H. C., Lee, P. K. D., Osorio, D., Ramsden, L., Yamashita, N., and Yuen, T.D.B. 2001. Field kit to characterize physical, chemical, and spatial aspects of potential primate foods. Folia Primatol. 72:11–25.PubMedCrossRefGoogle Scholar
  87. Lucas, P. W., Prinz, J. F., Agrawal, K. R., and Bruce, I. C. 2002. Food physics and oral physiology. Food Qual. Pref. 13:203–213.CrossRefGoogle Scholar
  88. Luschei, E. S., and Goodwin, G. M. 1974. Patterns of mandibular movement and jaw muscle activity during mastication in the monkey. J. Neurophysiol. 37:954–966.PubMedGoogle Scholar
  89. Marroig, G., De Vivo, M., and Cheverud, J.M. 2004. Cranial evolution in sakis (Pithecia, Platyrrhini) II: evolutionary processes and morphological integration. J. Evol. Biol. 17:144–155.PubMedCrossRefGoogle Scholar
  90. Martin, L. B., Olejniczak, A. J., and Maas, M. C. 2003. Enamel thickness and microstructure in pitheciin primates, with comments on dietary adaptations of the middle Miocene hominoid Kenyapithecus. J. Hum. Evol. 45:351–367.PubMedCrossRefGoogle Scholar
  91. Meldrum, D. J., and Kay, R. F. 1997. Nuciruptor rubricae, a new pitheciin seed predator from the Miocene of Colombia. Am. J. Phys. Anthropol. 102:407–427.PubMedCrossRefGoogle Scholar
  92. Miller, K. E., Bales, K. L., Ramos, J. H., and Dietz, J. M. 2006. Energy intake, energy expenditure, and reproductive costs of female wild golden lion tamarins (Leontopithecus rosalia). Am. J. Primatol. 68:1037–1053.PubMedCrossRefGoogle Scholar
  93. Milton, K. 1980. The foraging strategy of howler monkeys. New York: Columbia University Press.Google Scholar
  94. Milton, K. 1984a. The role of food-processing factors in primate food choice. In P. S. Rodman and J. G. H. Cant (eds), Adaptations for Foraging in Nonhuman Primates: Contributions to an Organismal Biology of Prosimians, Monkeys, and Apes (pp. 249–279). New York: Columbia University Press.Google Scholar
  95. Milton, K. 1984b. Protein and carbohydrate resources of the Maku Indians of north-western Amazonia. Am. Anthropol. 86:7–27.CrossRefGoogle Scholar
  96. Milton, K. 1984c. Habitat, diet, and activity patterns of free-ranging woolly spider monkeys (Brachyteles arachnoides E. Geoffroy 1806). Int. J. Primatol. 5:491–514.CrossRefGoogle Scholar
  97. Milton, K. 1988. Foraging behavior and the evolution of primate cognition. In A. Whiten and R. Byrne (eds.), Machiavellian Intelligence: Social Expertise and the Evolution of Intellect in Monkeys, Apes and Humans (pp. 285–305). Oxford UK: Oxford University Press.Google Scholar
  98. Milton, K. 1998. Physiological ecology of howlers (Alouatta): Energetic and digestive considerations and comparison with the Colobinae. Int. J. Primatol. 19:513–548.CrossRefGoogle Scholar
  99. Milton, K., Giacalone, J., Wright, S. J., and Stockmayer, G. 2005. Do frugivore population fluctuations reflect fruit production? Evidence from Panama. In J. L. Dew and J. P. Boubli (eds.), Tropical Fruits and Frugivores: The Search for Strong Interactors (pp. 5–35). Dordrecht, The Netherlands: Springer.CrossRefGoogle Scholar
  100. Moermond, T. C., and Denslow, J. S. 1985. Neotropical avian frugivores: patterns of behavior, morphology, and nutrition, with consequences for fruit selection. Ornithol. Mono. 36:865–897.Google Scholar
  101. Nash, L.T. 1984. Observations on the ecology and behavior of Galago senegalensis at the ADC Mutara Ranch, 29 July – 15 August, 1984. Rep. Inst. Prim. Res., Natl. Mus. Kenya.Google Scholar
  102. Nash, L.T. 1986. Dietary, behavioral, and morphological aspects of gummivory in primates. Yrbk. Phys. Anthropol. 29:113–137.CrossRefGoogle Scholar
  103. Nash, L.T. 1989. Galagos and gummivory. J. Hum. Evol. 4:199–206.CrossRefGoogle Scholar
  104. National Research Council 2003. Feeding ecology, digestive strategies, and implications for feeding programs in captivity. In Committee on Animal Nutrition, ad hoc committee on Nonhuman primate nutrition, Board on Agriculture and Natural Resources (eds.), Nutrient Requirements of Nonhuman Primates (pp. 5–40). Washington D.C.: The National Academies Press.Google Scholar
  105. Natori, M., and Shigehara, N. 1992. Interspecific differences in lower dentition among eastern-Brazilian marmosets. J. Mammal. 73:668–671.CrossRefGoogle Scholar
  106. Norconk, M. A. 1996. Seasonal variation in the diets of white-faced and bearded sakis (Pithecia pithecia and Chiropotes satanas) in Guri Lake, Venezuela. In M. A. Norconk, A. L. Rosenberger and P. A. Garber (eds.), Adaptive Radiations of Neotropical Primates (pp. 403–423). New York: Plenum.Google Scholar
  107. Norconk, M. A. 2007. Sakis, uakaris, and titi monkeys: behavioral diversity in a radiation of seed predators. In C. J. Campbell, A. Fuentes, K. C. MacKinnon, M. Panger, and S. K. Bearder (eds.), Primates in Perspective (pp. 123–138). Oxford UK: Oxford University PressGoogle Scholar
  108. Norconk, M. A., and Conklin-Brittain, N. L. 2004. Variation on frugivory: the diet of Venezuelan white-faced sakis. Int. J. Primatol. 25:1–26.CrossRefGoogle Scholar
  109. Norconk, M. A., Oftedal, O. T., Power, M. L., Jakubasz, M., and Savage, A. 2002. Digesta passage and fiber digestibility in captive white-faced sakis (Pithecia pithecia). Am. J. Primatol. 58:23–34.PubMedCrossRefGoogle Scholar
  110. Oftedal, O.T. 1991. The nutritional consequences of foraging in primates: the relationship of nutrient intakes to nutrient requirements. Phil. Trans. Roy. Soc. Lond., Ser. B. 334:161–170.CrossRefGoogle Scholar
  111. Palacios, E., Rodríguez, A., and Defler, T. R. 1997. Diet of a group of Callicebus torquatus lugens (Humboldt 1812) during the annual resource bottleneck in Amazonian Colombia. Int. J. Primatol. 18:503–522.CrossRefGoogle Scholar
  112. Peetz, A. 2001. Ecology and social organization of the bearded saki Chiropotes satanas chiropotes (Primates: Pitheciinae) in Venezuela. Ecol. Mono. 1:1–170.Google Scholar
  113. Peres, C. A., and Janson, C. H. 1999. Species coexistence, distribution and environmental determinants of Neotropical primate richness: a community-level zoogeographical analysis. In J. G. Fleagle, C. Janson and K. E. Reed (eds.), Primate Communities (pp. 55–74). Cambridge UK: Cambridge University Press.Google Scholar
  114. Pirie, P. L. 1976. Allometry in the Masticatory Apparatus of Primates. Ph.D. dissertation, Ohio State. University, Columbus, OH.Google Scholar
  115. Pirie, P. L. 1978. Allometric scaling in the postcanine dentition with reference to primate diets. Primates 19:583–591.CrossRefGoogle Scholar
  116. Podolsky, R. D. 1990. Effects of mixed-species association on resource use by Saimiri sciureus and Cebus apella. Am. J. Primatol. 21:147–158.CrossRefGoogle Scholar
  117. Porter, L. 2007. The Behavioral Ecology of Callimicos and Tamarins in Northwestern Bolivia. Pearson Prentice Hall, Upper Saddle River, NJ.Google Scholar
  118. Porter, L. M. 2001. Dietary differences among sympatric Callitrichinae in northern Bolivia: Callimico goeldii, Saguinus fuscicollis and S. labiatus. Int. J. Primatol. 22:961–992.CrossRefGoogle Scholar
  119. Porter, L. M., and Garber, P. A. 2004. Goeldi’s monkeys: a primate paradox? Evol. Anthropol. 13:104–115.Google Scholar
  120. Power, M. L., and Oftedal, O. T. 1996. Differences among captive callitrichids in the digestive responses to dietary gum. Am. J. Primatol. 40:131–144.CrossRefGoogle Scholar
  121. Power, M. L. 1996. The other side of callitrichine gummivory. In M. A. Norconk, A. L. Rosenberger, and P. A. Garber (eds.), Adaptive Radiations of Neotropical Primates (pp. 97–110). New York: Plenum.Google Scholar
  122. Rehg, J. A. 2006. Seasonal variation in polyspecific associations among Callimico goeldii, Saguinus labiatus, and S. fuscicollis in Acre, Brazil. Int. J. Primatol. 27:1399–1428.CrossRefGoogle Scholar
  123. Robbins, C. T. 1993. Wildlife Feeding and Nutrition. 2nd eition. Academic Press, San Diego.Google Scholar
  124. Rosenberger, A. L. 1978. Loss of incisor enamel in marmosets. J. Mammal. 59:207–208.CrossRefGoogle Scholar
  125. Rosenberger, A. L. 1983. Aspects of the systematics and evolution of the marmosets. In M. T. de Mello (ed.), A Primatologia no Brasil (pp. 159–180). Brasilia, Brazil: Sociedade Brasileira de Primatologia.Google Scholar
  126. Rosenberger, A. L. 1992. Evolution of feeding niches in New World monkeys. Am. J. Phys. Anthropol. 88:525–562.PubMedCrossRefGoogle Scholar
  127. Rosenberger, A. L., and Kinzey, W. G. 1976. Functional patterns of molar occlusion in platyrrhine primates. Am. J. Phys. Anthropol. 45:281–298.PubMedCrossRefGoogle Scholar
  128. Ross, C. F. 1995. Allometric and functional influences on primate orbit orientation and the origins of Anthropoidea. J. Hum. Evol. 29:201–227.CrossRefGoogle Scholar
  129. Russo, S. E., Campbell, C. J., Dew, J. L., Stevenson, P. R., and Suarez, S. A. 2005. A multi-forest comparison of dietary preferences and seed dispersal by Ateles spp. Int. J. Primatol. 26:1017–1038.CrossRefGoogle Scholar
  130. Russo, S. E. 2005. Linking seed fate to natural dispersal patterns: factors affecting predation and scatter-hoarding of Virola calophylla seeds in Peru. J. Trop. Ecol. 21:243–253.CrossRefGoogle Scholar
  131. Schumacher, G.H. 1961. Funktionelle Morphologie der Kaumuskulatur. Jena, Germany: Gustav Fischer.Google Scholar
  132. Setoguchi, T., and Rosenberger, A. 1987. A fossil owl monkey from La Venta, Colombia. Nature 326:692–694.PubMedCrossRefGoogle Scholar
  133. Silver, S. C., Ostro, L. E. T., Yeager, C. P., and Dierenfeld, E. S. 2000. Phytochemical and mineral components of foods consumed by black howler monkeys (Alouatta pigra) at two sites in Belize. Zoo Biol. 19:95–109.CrossRefGoogle Scholar
  134. Smith, A. C. 2000. Composition and proposed nutritional importance of exudates eaten by saddleback (Saguinus fuscicollis) and mustached (Saguinus mystax) tamarins. Int. J. Primatol. 21:69–83.CrossRefGoogle Scholar
  135. Smith, R. J. 1978. Mandibular biomechanics and temporomandibular joint function in primates. Am. J. Phys. Anthropol. 49:341–50.PubMedCrossRefGoogle Scholar
  136. Smith, R.J., and Jungers, W.L. 1997. Body mass in comparative primatology. J. Hum. Evol. 32:523–559.PubMedCrossRefGoogle Scholar
  137. Smith, R. J., Petersen, C. E., and Gipe, D. P. 1983. Size and shape of the mandibular condyle in primates. J. Morphol. 177:59–68.PubMedCrossRefGoogle Scholar
  138. Soini, P. 1993. The ecology of the pygmy marmoset, Cebuella pygmaea: some comparisons with two sympatric tamarins. In A. B. Rylands (ed.), Marmosets and Tamarins: Systematics, Behavior, and Ecology (pp. 257–261). Oxford UK: Oxford University Press.Google Scholar
  139. Spencer, M. A., and Spencer, G. S. 1995. Technical note: Video-based three-dimensional morphometrics. Am. J. Phys. Anthropol. 96:443–453.PubMedCrossRefGoogle Scholar
  140. Spencer, M. A. 2003. Tooth-root form and function in platyrrhine seed-eaters. Am. J. Phys. Anthropol. 122:325–335.PubMedCrossRefGoogle Scholar
  141. Starck, D. 1933. Die Kaumuskulatur der Platyrrhinen. Gegen. Morphol. Jahr. 72:212–285.Google Scholar
  142. Stevenson, P. R. 2001. The relationship between fruit production and primate abundance in Neotropical communities. Biol. J. Linn. Soc. 72:161–178.CrossRefGoogle Scholar
  143. Strier, K. B. 1991. Diet in one group of woolly spider monkeys, or muriquis (Brachyteles arachnoides). Am. J. Primatol. 23:113–126.CrossRefGoogle Scholar
  144. Strier, K. B. 1992. Ateline adaptations: behavioral strategies and ecological constraints. Am. J. Phys. Anthpol. 88:515–524.CrossRefGoogle Scholar
  145. Strier, K. B. 2006. Primate Behavioral Ecology. Pearson Allyn and Bacon, Boston, MA.Google Scholar
  146. Sussman, R. W., and Kinzey, W. G. 1984. The ecological role of the Callitrichidae: a review. Am. J. Phys. Anthropol. 64:419–449.PubMedCrossRefGoogle Scholar
  147. Talebi, M., Bastos, A., and Lee, P. C. 2005. Diet of southern muriquis in continuous Brazilian Atlantic forest. Int. J. Primatol. 26:1175–1187.CrossRefGoogle Scholar
  148. Taylor, A. B., and Vinyard, C. J. 2004. Comparative analysis of masseter fiber architecture in tree-gouging (Callithrix jacchus) and nongouging (Saguinus oedipus) callitrichids. J. Morphol. 261:276–285.PubMedCrossRefGoogle Scholar
  149. Teaford, M. F. 1985. Molar microwear and diet in the genus Cebus. Am. J. Phys. Anthropol. 66:363–370.PubMedCrossRefGoogle Scholar
  150. Teaford, M. F., Lucas, P. W., Ungar, P. S., and Glander, K. E. 2006. Mechanical defenses in leaves eaten by Costa Rican howling monkeys (Alouatta palliata). Am. J. Phys. Anthropol. 129:99–104.PubMedCrossRefGoogle Scholar
  151. Terborgh, J. 1983. Five New World Primates: a study in comparative ecology. Princeton University Press, Princeton, NJ.Google Scholar
  152. Thoren, S., Lindenfors, P., and Kappeler, P.M. 2006. Phylogenetic analyses of dimorphism in primates: Evidence for stronger selection on canine size than on body size. Am. J. Phys. Anthropol. 130:50–59.PubMedCrossRefGoogle Scholar
  153. Turnbull, W. D. 1970. Mammalian masticatory apparatus. Fieldiana, Geology 18:148–356.Google Scholar
  154. van Roosmalen, M. G. M. 1984. Subcategorizing foods in primates. In D. J. Chivers, B. A. Wood and A. Bilsborough (eds.), Food Acquisition and Processing in Primates (pp. 167–175). New York: Plenum Press.Google Scholar
  155. van Roosmalen, M. G. M. 1985. Habitat preferences, diet, feeding strategy and social organization of the black spider monkey (Ateles paniscus paniscus Linnaeus 1758) in Surinam. Acta Amazon. 15(3/4, suppl):1–238.Google Scholar
  156. van Roosmalen, M. G. M., Mittermeier, R. A., and Fleagle, J. G. 1988. Diet of the northern bearded saki (Chiropotes satanas chiropotes): A neotropical seed predator. Am. J. Primatol. 14:11–35.CrossRefGoogle Scholar
  157. Van Soest, P. J., Uden, P., and Wrick, K.F. 1983. Critique and evaluation of markers for use in nutrition of humans and farm and laboratory animals. Nutr. Rep. Int. 27:17–28.Google Scholar
  158. Veiga, L. M., and Ferrari, S. F. 2006. Predation of arthropods by southern bearded sakis (Chiropotes satanas) in eastern Brazilian Amazonia. Am. J. Primatol. 68:209–215.PubMedCrossRefGoogle Scholar
  159. Vinyard, C. J., and Ryan, T. M. 2006. Cross-sectional bone distribution in the mandibles of gouging and non-gouging platyrrhines. Int. J. Primatol. 27:1461–1490.CrossRefGoogle Scholar
  160. Vinyard, C. J., Wall, C. E., Williams, S. H., and Hylander, W. L. 2003. Comparative functional analysis of skull morphology of tree-gouging primates. Am. J. Phys. Anthropol. 120:153–170.PubMedCrossRefGoogle Scholar
  161. Vinyard, C. J., Wall, C. E., Williams, S. H., Johnson, K. R., and Hylander, W. L. 2006. Masseter electromyography during chewing in ring-tailed lemurs (Lemur catta). Am. J. Phys. Anthropol. 130:85–95.PubMedCrossRefGoogle Scholar
  162. Vinyard, C. J., Wall, C. E., Williams, S. H., Mork, A. L., Garner, B. A., Melo, L. C. O., Valença Montenegro, M. M., Valle, Y. B. M., Monteiro da Cruz, M. A., Lucas, P. W., Schmitt, D., Taylor, A. B., and Hylander, W. L. in press. The evolutionary morphology of tree gouging in marmosets. In S. M. Ford, L. M. Porter and L.C. Davis (eds.), The Smallest Anthropoids: The Marmoset/Callimico Radiation. New York: Springer.Google Scholar
  163. Wallace, R. B. 2005. Seasonal variations in diet and foraging behavior of Ateles chamek in a southern Amazonian tropical forest. Int. J. Primatol. 26:1053–1075.CrossRefGoogle Scholar
  164. Waterman, P., and Kool, K. M. 1994. Colobine food selection and plant chemistry. In A. G. Davies and J. F. Oates (eds.), Colobine monkeys: Their Ecology, Behavior and Evolution (pp.251–284). Cambridge UK: Cambridge University Press.Google Scholar
  165. Williams, S. H., Vinyard, C. J., Glander, K. E., Deffenbaugh, M., Teaford, M., and Thompson, C. L. 2008. A preliminary report on a telemetry system for assessing jaw-muscle function in free-ranging primates. Int. J. Primatol.Google Scholar
  166. Wrangham, R. W., Conklin, N. L., Etot, G., Obua, J., Hunt, K. D., Hauser, M. D., and Clark, A. P. 1993. The value of figs to chimpanzees. Int. J. Primatol. 14:243–256.CrossRefGoogle Scholar
  167. Wrick, K. L., Robertson, J. B., Van Soest, P. J., Lewis, B. A., Rivers, J. M., Roe, D. A., and Hackler, L.R. 1983. The influence of dietary fiber source on human intestinal transit and stool output. J. Nutr. 113:1464–1479.PubMedGoogle Scholar
  168. Wright, B. W. 2004. Ecological Distinctions in Diet, Food Toughness, and Masticatory Anatomy in a Community of Six Neotropical Primates in Guyana, South America. Ph.D. Dissertation. Urbana-Champaign: University of Illinois.Google Scholar
  169. Wright, B. W. 2005. Craniodental biomechanics and dietary toughness in the genus Cebus. J. Hum. Evol. 48:473–492.PubMedCrossRefGoogle Scholar
  170. Wright, K. W. 2005. Interspecific and Ontogenetic Variation in Locomotor Behavior, Habitat Use and Postcranial Morphology in Cebus apella and Cebus olivaceus. Ph.D. Dissertation. Northwestern University.Google Scholar
  171. Zar, J. H. 1999. Biostatistical Analysis. New York: Prentice Hall.Google Scholar
  172. Zingeser, M. R. 1973. Dentition of Brachyteles arachnoides with reference to Alouttine and Atelinine affinities. Folia Primatol. 20:351–390.PubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  • Marilyn A. Norconk
    • 1
  • Barth W. Wright
  • Nancy L. Conklin-Brittain
  • Christopher J. Vinyard
  1. 1.Department of Anthropology and School of Biomedical SciencesKent State UniversityKentUSA

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