The white-headed capuchin (Cebus capucinus), also known as the white-faced capuchin or white-throated capuchin, is a medium-sized New World monkey of the family Cebidae, subfamily Cebinae. Native to the forests of Central America and the extreme north-western portion of South America, the white-headed capuchin is important to rainforest ecology for its role in dispersing seeds and pollen.
Among the best known monkeys, the white-headed capuchin is recognized as the typical companion to the organ grinder. In recent years the species has become popular in North American media. It is a highly intelligent monkey and has been trained to assist paraplegic persons. It is a medium-sized monkey, weighing up to 3.9 kg (8.6 lb). It is mostly black, but with a pink face and white on much of the front part of the body, giving it its common name. It has a distinctive prehensile tail that is often carried coiled up and is used to help support the monkey when it is feeding beneath a branch.
In the wild, the white-headed capuchin is versatile, living in many different types of forest, and eating many different types of food, including fruit, other plant material, invertebrates, and small vertebrates. It lives in troops that can exceed 20 animals and include both males and females. It is noted for its tool use, including rubbing plants over its fur in an apparent use of herbal medicine, and also using tools as weapons and for getting to food. It is a long-lived monkey, with a maximum recorded age of over 54 years.
The white-headed capuchin was one of the many species originally described by Linnaeus in his 18th century work, Systema Naturae. It is a member of the family Cebidae, the family of New World monkeys containing capuchin monkeys, squirrel monkeys, tamarins and marmosets. It is the type species for the genus Cebus, the genus that includes all the capuchin monkeys. It is a member of the C. capucinus species group within the genus Cebus, a group that also includes the white-fronted capuchin, the weeper capuchin and the Kaapori capuchin.
There is disagreement among primatologists about whether there are any subspecies of white-headed capuchin. Some authorities consider there to be three subspecies of white-headed capuchin, based on small differences in appearance:
- C. c. capucinus, from the southern part of the range in Ecuador, Colombia and eastern Panama
- C. c. imitator, from most of Nicaragua, Costa Rica and western Panama
- C. c. limitaneus, from Honduras and northern Nicaragua
However, other authorities do not recognize any separate subspecies, and regard C. c. imitator and C. c. limitaneus as synonyms of C. capucinus.
Like other monkeys in the genus Cebus, the white-headed capuchin is named after the order of Capuchin friars – the cowls worn by these friars closely resemble the monkey's head coloration. The white-headed capuchin has mostly black fur, with white to yellowish fur on the neck, throat, chest, shoulders, and upper arms. The face is pink. A V-shaped area of black fur on the crown of the head is distinctive. It has a prehensile tail that is often held coiled, giving the white-headed capuchin the nickname "ringtail".
Adults reach a length of between 335 and 453 mm (13.2 and 17.8 in), excluding tail, and a weight of up to 3.9 kg (8.6 lb). The tail is longer than the body, at up to 551 mm (21.7 in) in length. Males are about 27% larger than females. The brain of a white-headed capuchin is about 79.2 g (2.79 oz), which is larger than that of several larger monkey species, such as the Mantled Howler.
The white-headed capuchin is a diurnal and arboreal animal. However, it does come down to the ground more often than many other New World monkeys. It moves primarily by walking on all four limbs. It lives in troops, or groups, of up to 40 monkeys (mean 16, range 4-40) and has a male/female adult sex ratio of .71 on average (range .54-.88). With rare exceptions, females spend their entire lives with their female kin. Males migrate to new social groups multiple times during the course of their lifetimes, migrating for the first time between 20 months and 11 years of age. The median age of migration in the Santa Rosa population is 4.5 years. Males sometimes migrate alone, but more often they migrate in the company of other males who are often their kin. One of the unusual features of the kinship structure of the white-headed capuchin, relative to other primate species, is the high degree of relatedness within groups that results from the long tenures of alpha males who sire most of the offspring. Alpha males have been known to keep their positions as long as 17 years in this species and this puts them in the unusual position of being available to sire the offspring of their daughters and granddaughters, who produce their first offspring at about 6–7 years of age. Typically, however, alpha males do not breed with their own daughters, even though they do sire virtually all offspring produced by females unrelated to them. Those subordinate males who are allies of the alpha male in group defense are the males who sire the offspring of the alpha male's daughters. The high degree to which alpha males monopolize matings results in an unusually large number of paternal half-siblings and full siblings in this species relative to other primate species.
Kinship is an important organizing factor in the structuring of female-female social relationships. Particularly in larger groups, females preferentially associate with, groom, and provide coalitionary support to their matrilineally related female kin. They do not exhibit a similar preference for their paternal half sisters, which may mean that they only are capable of recognizing kinship through the maternal line. Dominance rank is also an important organizing factor, with females more often grooming and associating with females who are closer to them in the dominance hierarchy. Female-female dyads groom far more than male-female and male-male dyads. Coalitionary aggression is common both among males and females, and capuchins seem to have an excellent understanding of the alliance structure in their group. For example, when capuchins are fighting, they sensibly recruit aid from someone who is both higher ranking than they are and also better friends with themselves than with their opponent.
Female capuchins have linear dominance hierarchies. In contrast to many Old World monkeys such as macaques, in which females socially inherit the rank just below their mothers and just above their next oldest sisters, capuchins do not have a highly predictable ranking within their matrilines. Males are typically dominant to females. The alpha male is always easy to discern, but there are sometimes ambiguous rankings among subordinate males. Male-male relationships are tense, and affiliation between males is typically expressed by resting in contact, playing, or non-conceptive sex rather than by grooming. Males cooperate in coalitions against potential predators, and also in defense of the group against other males. Occasionally male coalitionary aggression becomes so violent that males are killed, particularly if they are encountered roaming the forest unaccompanied by allies. Because aggression from other male capuchins is the leading cause of death (aside from poaching by humans, where there is contact between humans and capuchins), male allies are critical for self-defense during migration, and to assist in taking over other groups. Male emigration to a new troop typically occurs about every 4 years, so most males are in constant danger of having to defend themselves against other groups of males.
Immigrating males often kill young infants when they take over a group. Females band together to defend their infants from infanticidal males, but they rarely succeed in saving their infants. Because infants inhibit their mothers from ovulating by nursing frequently, males are able to bring females into estrus earlier by killing the infants and thereby terminating nursing; this has the effect of increasing their breeding opportunities. Females do often mate with the killers of their infants, and with time, they typically become as supportive of the new alpha male as they had been of the previous one. The alpha male helps defend females from subordinate males within the group as well as from infanticidal males from other groups.
Interactions between groups
White-faced capuchin troops occupy home ranges of between 32 and 86 hectares (79 and 210 acres). They travel between 1 and 3 kilometres (0.62 and 1.9 mi) daily, averaging 2 kilometres (1.2 mi) per day. Although they engage in activity that has been described as "territorial", more recent research indicates that White-faced capuchin troops tend to behave aggressively to other White-faced capuchin troops regardless of where they meet, and the aggression is not necessarily intended to exclude the other troops from a specific home range.
Home ranges overlap extensively, so groups are not territorial in the strictest sense of the word. Perhaps because of the intensity of male-male competition and the threat of infanticide, interactions between groups are typically hostile: the males display aggressively toward one another and sometimes engage in physical aggression (even killing an opponent), while females grab their infants and run. Typically, males are the primary participants in aggressive intergroup encounters, and it seems likely that males are defending access to the females in their groups. Alpha males, who have the largest reproductive stake in the group, participate at a higher rate than subordinate males. Groups with more males have an advantage over groups with fewer males, but the location of the encounter within the home range matters as well; smaller groups defeat larger groups when the contest occurs in the core or center area of the smaller group's home range.
The white-headed capuchin sometimes interacts with other sympatric monkey species. White-headed capuchins sometimes travel with and even groom Geoffroy's Spider Monkeys. However, aggressive interactions between the capuchins and spider monkeys also occur. Interactions between the white-headed capuchin and mantled howler are infrequent, and sometimes result in the capuchins threatening the larger howlers. However, affiliative associations between the capuchins and howlers do sometimes occur, mostly involving juveniles playing together.
Although South American capuchin species often travel with and feed together with squirrel monkeys, the white-headed capuchin only rarely associates with the Central American squirrel monkey. This appears to be related to the patchier, more dispersed distribution of food resources in Central America and the fact that there is less dietary overlap between the Central American squirrel monkey and the white-headed capuchin than between their South American counterparts. Therefore, there is less benefit to the Central American squirrel monkey in associating with the white-headed capuchin in order to exploit the capuchin's knowledge of food resource distribution. In addition, compared to their South American counterparts, male white-headed capuchins are relatively more alert to rival males than to predators, reducing the predator detection benefits that the Central American squirrel monkey receives from associating with the white-headed capuchin compared to its South American counterparts. Since the squirrel monkeys generally initiate interactions with the capuchins in South America, the fact that similar associations would impose higher foraging costs and impart fewer predator detection benefits to the Central American squirrel monkey leads to fewer associations with the white-headed capuchin.
Several non-primate animal species tend to follow troops of White-faced Monkeys or are otherwise attracted by their presence. white-lipped peccaries and common agoutis are attracted by feeding white-headed capuchins, looking for fruit that the capuchins drop. Several species of bird are also known to follow white-headed capuchins looking for food. These include the double-toothed kite, the white hawk and the sharp-shinned hawk.
The white-headed capuchin is an omnivore. Its primary foods are fruit and insects. It forages at all levels of the forest, and also forages on the ground. Methods for finding food include stripping bark off of trees, searching through leaf litter, breaking dead tree branches, rolling over rocks, and using stones as anvils to crack hard fruits. Its prehensile tail assists with feeding, helping support the monkey when foraging for food below the branches.
Fruit can make up between 50% and 67% or more of the capuchin's diet. In one study in Panama, white-headed capuchins ate 95 different fruit species. Among its favorite fruits are figs from the family Moraceae, mangos and related fruits from the family Anacardiaceae, the bean-like fruits from the family Leguminosae and fruits from the family Rubiaceae. It generally only eats ripe fruit, testing for ripeness by smelling, tasting and prodding the fruit. It typically eats only the pulp and juice, spitting out the seeds and fibers. Other plant matter eaten includes flowers, young leaves, seeds of certain plants, and bromeliads. It also uses the bromelids as a water source, drinking the water that gets trapped inside.
Insect prey eaten includes beetle larvae, butterfly and moth caterpillars, ants, wasps, and ant and wasp larvae. It also eats larger prey, such as birds, bird eggs, frogs, lizards, crabs, mollusks and small mammals. The population in Guanacaste, Costa Rica in particular is noted for hunting squirrels, magpies, White-crowned Parrots and baby coatis. The amount of vertebrate prey eaten varies by troop. Even neighboring troops can show significant differences in their diets.
The diet can vary between the rainy and dry season. For example, in Guanacaste, Costa Rica the white-headed capuchin can eat a wide variety of fruits as well as caterpillars in the early rainy season (June to November). But during the dry season, only figs and a few other types of fruit are available. During the dry season, chitinous insects, ant and wasp larvae and vertebrates become a particularly important part of the white-headed capuchin's diet. Access to water can also become an issue during the dry season. The white-headed capuchin likes to drink daily, so in forests where water holes dry up during the dry season, there can be competition between troops over access to the remaining water holes.
Capuchins are considered among the most intelligent of the New World monkeys; they have been the subject of many studies on behaviour and intelligence. The capuchins' intelligence is thought to be an adaptation to support their feeding habits; they rely on ephemeral food sources which may be hard to find. In one particular study conducted in 2007, capuchins were found to be among the ten most intelligent primates, second to spider monkeys among New World monkeys.
The white-headed capuchin is known to rub parts of certain plants into their fur. Plants used in this manner include citrus fruits, vines of the genera Piper and Clematis, monkey comb (genus Sloanea), dumb cane and custard apple. Ants and millipedes are also used in this way. It is not definitively known what this fur rubbing is for, but this may deter parasites such as ticks and insects, or it may serve as a fungicide or bactericide or anti-inflammatory agent. Alternatively, it may be a form of scent marking.
The white-headed capuchin also uses tools in other ways. It has been known to beat snakes with sticks in order to protect itself or to get the snake to release an infant. In captivity, it has been known to use tools to get to food or to defend itself, and in one case a white-headed capuchin used a squirrel monkey as a projectile, hurling it at a human observer. Some populations also use trees or other hard surfaces as anvils in order to crack mollusks. And it sometimes uses sticks as probes to explore openings.
The white-headed capuchin's intelligence and ability to use tools allows them to be trained to assist paraplegics. Other species of capuchin monkeys are also trained in this manner. White-headed capuchins can also be trained for roles on television and movies, such as Marcel on the television series Friends. They were also traditionally used as organ grinder monkeys.
The white-headed capuchin is noisy. Loud calls, such as barks and coughs, are used to communicate threat warnings, and softer calls, such as squeals, are used in intimate discourse. Different types of threats, such as a threat from a terrestrial animal versus a threat from a bird, invoke different vocalizations. Facial expressions and scent are also important to communication. It sometimes engages in a practice known as "urine washing", in which the monkey rubs urine on its feet. The exact purpose of this practice is unknown, but it may be a form of olfactory signal.
The white-headed capuchin uses a polygamous mating system in which a male may mate with multiple females. Although the dominant male does not monopolize breeding, studies have shown that the dominant male does tend to father most of the young. Although a female may mate with several males, the dominant male may be more likely to copulate when the female is at peak fertility. Nonetheless, there is evidence that dominant males do tend to avoid breeding with their own daughters who are members of the troop. Such avoidance is rare among New World primates.
Copulation takes about 2 minutes, and the gestation period is 5 to 6 months. Usually a single young is born, but twins occur occasionally. Most births occur during the dry season from December to April. The infant is carried across its mother's back for about 6 weeks. After about 4 to 5 weeks it can stray from its mother for brief periods and by about 3 months it can move around independently, although some infants will be mostly independent earlier. Weaning occurs between 6 and 12 months. While the mother rests, the young spends most of its time foraging or playing, either on its own or with other juveniles. Capuchins engage in high levels of alloparenting, in which monkeys other than the mother help care for the infant. Infants are carried by alloparents most often between 4 and 6 weeks in age. Males as well as females engage in alloparenting.
Like other capuchin species, the white-headed capuchin matures slowly. Sexual maturity can be reached at 3 years. But on average, females give birth for the first time at 7 years old and give birth every 26 months thereafter. Males attain reproductive maturity at 10 years old. The white-headed capuchin has a long life span given its size. The maximum recorded life span in captivity is over 54 years.
Distribution and habitat
The white-headed capuchin is found in much of Central America and a small portion of South America. In Central America, its range includes much of Honduras, Nicaragua, Costa Rica and Panama. It has also been reported to occur in eastern Guatemala and southern Belize, but these reports are unconfirmed. In South America the white-headed capuchin is found in the extreme north-western strip between the Pacific Ocean and the Andes Mountains in Colombia and northwestern Ecuador. It is among the most commonly seen monkeys in Central America's national parks, such as Manuel Antonio National Park, Corcovado National Park, Santa Rosa National Park and Soberania National Park.
It is found in many different types of forest, including mature and secondary forests, and including evergreen and deciduous forests, dry and moist forests, and mangrove and montane forests. However, it appears to prefer primary or advanced secondary forests. Also, higher densities of white-headed capuchins are found in older areas of forest and in areas containing evergreen forest, as well as areas with more water availability during the dry season.
The white-headed capuchin is regarded as "least concern" from a conservation standpoint by IUCN. However, its numbers are impacted by the fact that it is sometimes captured for the pet trade. Its status can also be harmed by deforestation. However, deforestation may also impact its main predator, the Harpy Eagle, more than it directly impacts the white-headed capuchin, and so on a net basis deforestation may not be as harmful to the capuchin's status. The white-headed capuchin can adapt to forest fragmentation better than other species due to its ability to live in a wide variety of forest types and exploit a wide variety of food sources. The white-headed capuchin is important to its ecosystems as a seed and pollen disperser. It also impacts the ecosystem by eating insects that act as pests to certain trees, by pruning certain trees, such as Gustavia superba and Bursera simaruba, causing them generate more branches and possibly additional fruit, and by accelerating germination of certain seeds when they pass through the capuchin's digestive tract. In addition, the white-headed capuchin sometimes kills Acacia collinsii plants when it rips through the plant's branches to get to resident ant colonies.
- ^ a b Groves, C. (2005). Wilson, D. E., & Reeder, D. M, eds. ed. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. pp. 137. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=12100270.
- ^ Causado, J., Cuarón, A.D., Shedden, A., Rodríguez-Luna, E. & de Grammont, P.C. (2008). "Cebus capucinus". IUCN Red List of Threatened Species. Version 2011.2. International Union for Conservation of Nature. http://www.iucnredlist.org/apps/redlist/details/40020. Retrieved 19 January 2012.
- ^ a b c d e Rylands, A., Groves, C., Mittermeier, R., Cortes-Ortiz, L., and Hines, J. (2006). "Taxonomy and Distributions of Mesoamerican Primates". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 40–43. ISBN 0-387-25854-X.
- ^ (Latin) Linnaeus, C (1758). Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Editio decima, reformata. Holmiae. (Laurentii Salvii).
- ^ a b Groves, C. (2005). Wilson, D. E., & Reeder, D. M, eds. ed. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. p. Cebus. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=12100255.
- ^ "Capuchin Franciscans F.A.Q.". Capuchin Franciscans Vocation Office Province of Saint Joseph. http://capuchinfranciscans.org/sub_faq.html. Retrieved 2008-09-01.
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y Wainwright, M. (2002). The Natural History of Costa Rican Mammals. Zona Tropical. pp. 135–139. ISBN 0-9705678-1-2.
- ^ a b c d e f g h i Emmons, L. (1997). Neotropical Rainforest Mammals A Field Guide (Second ed.). University of Chicago Press. pp. 130–131. ISBN 0-226-20721-8.
- ^ a b c d e f g Rowe, N. (1996). The Pictorial Guide to the Living Primates. Pogonias Press. p. 95. ISBN 0-9648825-0-7.
- ^ "Medical Dictionary Capuchin Monkey". Farlex Inc.. http://medical-dictionary.thefreedictionary.com/Capuchin+(monkey). Retrieved 2008-09-01.
- ^ a b c d e Jack, K. (2007). "The Cebines". In Campbell, C., Fuentes, A., MacKinnon, K., Panger, M., & Bearder, S. Primates in Perspective. Oxford University Press. pp. 107–120. ISBN 978-0-19-517133-4.
- ^ Rowe, N. (1996). The Pictorial Guide to the Living Primates. Pogonias Press. p. 109. ISBN 0-9648825-0-7.
- ^ Morris, D. & Bruce, D. (2005). Primate Ethology. Aldine Transaction. pp. 237–238. ISBN 020230826X.
- ^ Bezanson, L. (2006). "Ontogenetic Influences on Positional Behavior in Cebus and Alouatta". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 333–344. ISBN 0-387-25854-X.
- ^ a b Fragaszy, D., Visalberghi, E. & Fedigan, L. (2004). "Life History and Demography". The Complete Capuchin. Cambridge University Press. p. 77.
- ^ Jack, K & Fedigan, L. (2009). "Female dispersal in a female-philopatric species, Cebus capucinus.". Behaviour 146: 471–498. doi:10.1163/156853909X404420.
- ^ a b c d e f g h i Perry, Susan; Manson, Joseph (2008). Manipulative Monkeys: The Capuchins of Lomas Barbudal. Cambridge, MA: Harvard University Press. p. 118. ISBN 978-0-674-02664-3.
- ^ Fragaszy, D., Visalberghi, E. & Fedigan, L. (2004). "Life History and Demography". The Complete Capuchin. Cambridge University Press. p. 79.
- ^ Jack, K & Fedigan, L. (2004). "Male dispersal patterns in white-faced capuchins, Cebus capucinus Part 1: patterns and causes of natal emigration". Animal Behaviour 67: 761–769. doi:10.1016/j.anbehav.2003.04.015.
- ^ Jack, K & Fedigan, L. (2004). "Male dispersal patterns in white-faced capuchins, Cebus capucinus Part 2: Patterns and causes of secondary dispersal". Animal Behaviour 67: 771–782. doi:10.1016/j.anbehav.2003.06.015.
- ^ a b Perry, Susan; Manson, Joseph (2008). Manipulative Monkeys: The Capuchins of Lomas Barbudal. Cambridge, MA: Harvard University Press. ISBN 978-0-674-02664-3.
- ^ Jack, K & Fedigan, L. (2004). "Male dispersal patterns in white-faced capuchins, Cebus capucinus Part 1: patterns and causes of natal emigration". Animal Behaviour 67: 761–769. doi:10.1016/j.anbehav.2003.04.015.
- ^ Perry unpublished data:Lomas Barbudal, Costa Rica
- ^ a b Jack, K & Fedigan, L. (2004). "Male dispersal patterns in white-faced capuchins, Cebus capucinus Part 1: patterns and causes of natal emigration.". Animal Behaviour 67: 761–769. doi:10.1016/j.anbehav.2003.04.015.
- ^ Jack, K & Fedigan, L. (2004). "Male dispersal patterns in white-faced capuchins, Cebus capucinus Part 2: Patterns and causes of secondary dispersal.". Animal Behaviour 67: 771–782. doi:10.1016/j.anbehav.2003.06.015.
- ^ a b Perry, Susan; Manson, Joseph (2008). Manipulative Monkeys: The Capuchins of Lomas Barbudal. Cambridge, MA: Harvard University Press. pp. 145–154, 169–214. ISBN 978-0-674-02664-3.
- ^ Perry, Susan; Manson, Joseph (2008). Manipulative Monkeys: The Capuchins of Lomas Barbudal. Cambridge, MA: Harvard University Press. ISBN 978-0-674-02664-3.
- ^ a b c Muniz, L., Perry, S., Manson, J., Gilkenson, H., Gros-Louis, J., & Vigilant, L. (2006). "Father-daughter inbreeding avoidance in a wild primate population.". Current Biology 16 (5): 156–7. doi:10.1016/j.cub.2006.02.055. PMID 16527729.
- ^ a b c d e f g h Perry, S., Manson, J.H., Muniz, L., Gros-Louis, J., & Vigilant, L. (2008). "Kin-biased Social Behaviour in Wild Adult Female White-faced Capuchins (Cebus capucinus)". Animal Behaviour 76: 187–199. doi:10.1016/j.anbehav.2008.01.020.
- ^ Fragaszy, D., Visalberghi, E. & Fedigan, L. (2004). "Life History and Demography". The Complete Capuchin. Cambridge University Press. p. 74.
- ^ a b Perry, S. (1996). "Female-female relationships in wild white-faced capuchin monkeys, Cebus capucinus.". American Journal of Primatology 40: 167–182. doi:10.1002/(SICI)1098-2345(1996)40:2<167::AID-AJP4>3.0.CO;2-W.
- ^ Perry, S., Manson, J. & Barrett, H.C. (2004). "White-faced capuchin monkeys exhibit triadic awareness in their choice of allies.". Animal Behaviour 67: 165–170. doi:10.1016/j.anbehav.2003.04.005.
- ^ Bergstrom, M. & Fedigan, L.M. (2009). "Strength and stability of dominance hierarchies in female white-faced capuchins (Cebus capucinus) at Santa Rosa National Park, Costa Rica.". American Journal of Primatology (supplement) 71: 103.
- ^ Perry, S. (1997). "Male-female social relationships in wild white-faced capuchin monkeys, Cebus capucinus.". Behaviour 134: 477–510. doi:10.1163/156853997X00494.
- ^ a b c Perry,S. (1998). "Male-male social relationships in wild white-faced capuchins, Cebus capucinus.". Behaviour 135: 1–34.
- ^ Manson, J.H., Perry, S. & Parish, A.R. (1997). "Nonconceptive sexual behavior in bonobos and capuchins.". International Journal of Primatology 18: 767–786. doi:10.1023/A:1026395829818.
- ^ Perry, S. (1996.). "Intergroup encounters in wild white-faced capuchins, Cebus capucinus.". International Journal of Primatology 17: 309–330. doi:10.1007/BF02736624.
- ^ a b Gros-Louis, J., Perry, S. & Manson, J.H. (2003). "Violent coalitionary attacks and intraspecific killing in wild capuchin monkeys (Cebus capucinus).". Primates 44 (4): 341–346. doi:10.1007/s10329-003-0050-z. PMID 12910384.
- ^ a b Fedigan, L. & Jack, K. (2004). "The Demographic and Reproductive Context of Male Replacements in Cebus Capucinus" (PDF). Behaviour 141: 755–775. doi:10.1163/1568539042245178. http://www.ucalgary.ca/~fedigan/Beh%20Fedigan%20and%20Jack%202004.pdf. Retrieved 2008-11-14.
- ^ a b c Jack, K. & Fedigan, L. (2006). "Dominance and Reproductive Success in Wild White-Faced Capuchins". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 367–382. ISBN 0-387-25854-X.
- ^ Manson JH, Gros-Louis J, & Perry S. (2004). "Three apparent cases of infanticide by males in wild white-faced capuchins (Cebus capucinus)". Folia Primatologica 75 (2): 104–106. doi:10.1159/000076270. PMID 15010584.
- ^ a b Fedigan, L.M. (2003). "Impact of male takeovers on infant deaths, births, and conceptions in Cebus capucinus at Santa Rosa, Costa Rica.". International Journal of Primatology 24: 723–741. doi:10.1023/A:1024620620454.
- ^ Hrdy, S. (1974). "Male-male competition and infanticide among the langurs (Presbytis entellus) of Abu, Rajasthan.". Folia Primatologica 22: 19–58. doi:10.1159/000155616. PMID 4215710.
- ^ Perry, S. (1997). "Male-female social relationships in wild white-faced capuchin monkeys, Cebus capucinus". Behaviour 134: 477–510. doi:10.1163/156853997X00494.
- ^ a b c d e f g h i j k l m n o Defler, T. (2004). Primates of Colombia. Bogotá, D.C., Colombia: Conservation International. pp. 227–235. ISBN 1-881-17383-6.
- ^ Fragaszy, D., Visalberghi, E., & Fedigan, L. (2004). "Behavioral Ecology". The Complete Capuchin. Cambridge University Press. pp. 38–39. ISBN 0521667682.
- ^ a b c d Perry, S. (1996). "Intergroup encounters in wild white-faced capuchins, Cebus capucinus.". International Journal of Primatology 17: 309–330. doi:10.1007/BF02736624.
- ^ a b Crofoot, M.C., Gilby, I.C., Wikelski, M.C,& Kays, RW (2008). "Interaction location outweighs the competitive advantage of numerical superiority in Cebus capucinus intergroup contests.". PNAS 105 (2): 577–581. doi:10.1073/pnas.0707749105. PMC 2206578. PMID 18184811. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2206578.
- ^ a b Rose, L., Perry, S., Panger, M., Jack, K., Manson, J., Gros-Louis, J., and Mackinnin, K. (August 2003). "Interspecific Interactions between Cebus capucinus and other Species: Data from Three Costa Rican Sites" (PDF). International Journal of Primatology 24 (4): 780–785. doi:10.1023/A:1024624721363. http://people.ucsc.edu/~evogel/cv/Roseetal2003.pdf.
- ^ Boinski, S. (2000). "Social Manipulation Within and Between Troops Mediates Primate Group Movement". In Boinski, S. and Garber, P.. On the Move. The University of Chicago Press. pp. 447–448. ISBN 0-226-06340-2.
- ^ Boinski, S. (April, 1989). "Why don’t Saimiri oerstedii and Cebus capucinus form mixed-species groups?". International Journal of Primatology 10 (2): 103–114. doi:10.1007/BF02736248.
- ^ Fragaszy, D., Visalberghi, E., & Fedigan, L. (2004). "Community Ecology". The Complete Capuchin. Cambridge University Press. p. 70. ISBN 0521667682.
- ^ a b Chapman, C. & Fedigan, L. (1990). "Dietary Differences between Neighboring Cebus capucinus Groups: Local Traditions, Food Availability or Responses to Food Profitability?" (PDF). Folia Primatol 54 (3-4): 177–186. doi:10.1159/000156442. PMID 2391047. http://www.arts.mcgill.ca/programs/anthro/chapman_files/CWeb/Pdf/33_CRNeighboringCebus.pdf.
- ^ a b c d e Fragaszy, D., Visalberghi, E., & Fedigan, L. (2004). "Behavioral Ecology". The Complete Capuchin. Cambridge University Press. pp. 43–47. ISBN 0521667682.
- ^ MacKinnon, K. (2006). "Food Choice by Juevenile Capuchin Monkeys". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 354–360. ISBN 0-387-25854-X.
- ^ a b c David Attenborough (2003). Life of Mammals. BBC Video.
- ^ Perry S. Rose L. (1994). Begging and transfer of coati meat by white-faced capuchin monkeys, Cebus capucinus. Primates 35 (4): 409-415
- ^ Leake, D. & Dobson, R. (April 15, 2007). "Chimps Knocked Off Top of the IQ Tree". The Times (London). http://www.timesonline.co.uk/tol/news/uk/article1654998.ece. Retrieved 2008-09-01.
- ^ Fragaszy, D., Visalberghi, E., & Fedigan, L. (2004). "Capuchins Use Objects as Tools". The Complete Capuchin. Cambridge University Press. pp. 173–183. ISBN 0521667682.
- ^ "Capuchin Monkey (Cebus capucinus)". The Rainforest Alliance. http://www.rainforest-alliance.org/resources.cfm?id=capuchin_monkey. Retrieved 2009-02-07.
- ^ Blumenthal, D. (June 17, 1987). "Monkeys as Helpers To Quadriplegics At Home". The New York Times.
- ^ Pflum, M. (March 18, 2000). "Earth Matters: Turkey struggles with national epidemic: primate smuggling". CNN. http://www.monkeyworld.co.uk/press.php?ArticleID=15. Retrieved 2009-02-07.
- ^ a b c d Henderson, C. (2000). Field Guide to the Wildlife of Costa Rica. University of Texas Press. pp. 454–455. ISBN 0-292-73459-X.
- ^ a b Fragaszy, D., Visalberghi, E., & Fedigan, L. (2004). "Social Interactions, Relationships and Social Structure". The Complete Capuchin. Cambridge University Press. pp. 202–220. ISBN 0521667682.
- ^ Fragaszy, D., Visalberghi, E., & Fedigan, L. (2004). "The Body". The Complete Capuchin. Cambridge University Press. p. 102. ISBN 0521667682.
- ^ Carnegie, S., Fedigan, L. & Ziegler, T. (2006). "Post-conceptive Mating in White-Faced Capuchins". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 387–405. ISBN 0-387-25854-X.
- ^ a b Di Fiore, A. (2009). "Genetic Approaches to the Study of Dispersal and Kinship in New World Primates". In Garber, P., Estrada, A., Bicca-Marques, J.C., Heymann, E. & Strier, K. South American Primates: Comparative Perspectives in the Study of Behavior, Ecology and Conservation. Springer. pp. 222–223. ISBN 978-0-387-78704-6.
- ^ Panger, M., Perry, S., Rose, L., Gros-Louis, J., Vogel,E., Mackinnon, C. & Baker, M. (2002). "Cross-Site Differences in Foraging Behavior of White-Faced Capuchins (Cebus capucinus)". American Journal of Physical Anthropology 119: 54. http://people.ucsc.edu/~njdominy/people/pdf/Panger_et_al.pdf.
- ^ a b Perry, S. (2008). Manipulative Monkeys: The Capuchins of Lomas Barbudal. Harvard University Press. pp. 229–241. ISBN 0-674-02664-0.
- ^ Hunter, L. & Andrew, D. (2002). Watching Wildlife Central America. Lonely Planet Publications. pp. 97, 100, 110, 130. ISBN 1-86450-034-4.
- ^ DeGama, H. and Fedigan, L. (2006). "The Effects of Forest Fragment Age, Isolation, Size, Habitat Type, and Water Availability on Monkey Density in a Tropical Dry Forest". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 165–186. ISBN 978-0-387-25854-6.
- ^ Garber, P., Estrada, A., and Pavelka, M. (2006). "Concluding Comments and Conservation Priorities". In Estrada, A., Garber, P., Pavelka, M. & Luecke, L. New Perspectives in the Study of Mesoamerican Primates. New York: Springer. pp. 570–571. ISBN 0-387-25854-X.