Cebus albifronswhite-fronted capuchin

Ge­o­graphic Range

Cebus alb­ifrons is found in north­west­ern South Amer­ica, in­clud­ing Ecuador, Colom­bia, Venezuela, east­ern Peru, and much of Ama­zon­ian Brazil (Hill, 1960).

Habi­tat

White-fronted ca­puchins are found in rain­for­est habi­tats from sea-level to 2000 me­ters (Hill, 1960).

Phys­i­cal De­scrip­tion

Cebus alb­ifrons is one of the smaller species of the ca­puchin group. The head is small in com­par­i­son to the body and the torso is slen­der with long, nar­row limbs. C. alb­ifrons has a com­plex color pat­tern. Over­all they are light brown on the back with a lighter ven­tral side, often in shades of yel­low and red. Dor­sal fur is long and soft, which con­trasts to the short and coarser fur of the ven­ter. The crown of the head has a round, dark patch. Fe­males may have a tuft of hair an­te­rior to this patch. The face is cov­ered by sparse, pale col­ored hair under which the peach col­ored flesh is vis­i­ble. A thin bor­der of white sur­rounds the face. A stripe, slightly darker than the body color, runs par­al­lel to the spine. The limbs are a range of yel­lows and red browns. Sex­ual di­mor­phism oc­curs in the species with the males being larger than the fe­males, the tail of the male may be lighter at the tip. Sea­sonal coat changes can occur; in the dry sea­son, the coat is over­all paler, in the rainy sea­son the coat dark­ens (Hill, 1960).

  • Sexual Dimorphism
  • male larger
  • Range mass
    1100 to 3300 g
    38.77 to 116.30 oz

Re­pro­duc­tion

As in other Cebus species, C. alb­ifrons does not ap­pear to have a breed­ing sea­son, though most births may co­in­cide with the dry sea­son (Nowak, 1991). Peak mat­ing pe­ri­ods are de­ter­mined by ge­o­graphic lo­ca­tion. Fe­males in es­trus ac­tively re­spond to males who seek to mate. It ap­pears that males may be able to de­tect fe­males in es­trus by chem­i­cal cues in her urine (Smuts et al., 1987).

Cebus alb­ifrons gives birth to a sin­gle young every 1 to 2 years, with a ges­ta­tion pe­riod of about 150 to 160 days. If the in­fant dies shortly after birth, the fe­male mates in the next breed­ing sea­son, but if the in­fant lives, the fe­male post­pones breed­ing an extra year in order to take care of the in­fant (Smuts et al., 1987).

  • Breeding interval
    Cebus albifrons gives birth to a single young every 1 to 2 years
  • Breeding season
    Peak mating periods are determined by geographic location.
  • Average number of offspring
    1
  • Average number of offspring
    1
    AnAge
  • Range gestation period
    150 to 160 days
  • Average age at sexual or reproductive maturity (female)
    Sex: female
    1310 days
    AnAge
  • Average age at sexual or reproductive maturity (male)
    Sex: male
    1310 days
    AnAge

In­fant care is not re­stricted to the ma­ter­nal fe­male in C. alb­ifrons. Other group mem­bers will come to the aid of in­fants in dis­tress and dom­i­nant males often care for in­fants. When in­fants are under 2 months old other fe­males care for, nurse, and feed them (Smuts et al., 1987).

Males dis­perse from their natal group upon reach­ing sex­ual ma­tu­rity, fe­males re­main with their natal group.

  • Parental Investment
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • male
      • female
  • pre-independence
    • protecting
      • male
      • female
  • post-independence association with parents

Lifes­pan/Longevity

Be­hav­ior

Group size ranges from 15 to 35 mem­bers. Groups are typ­i­cally led by a dom­i­nant male and fe­male. Ag­gres­sive in­ter­ac­tions con­sti­tute only about 10% of so­cial in­ter­ac­tions. White-fronted ca­puchins are highly so­cial and spend a lot of time in rec­i­p­ro­cal groom­ing, how­ever, dom­i­nant males and fe­males re­ceive a large pro­por­tion of groom­ing and rarely groom other in­di­vid­u­als (Smuts et al., 1987).

The small size of white-fronted ca­puchins makes them vul­ner­a­ble to larger preda­tors. These ca­puchins have adopted a loud alarm call which scares some preda­tors off and may warn oth­ers in the group about the pres­ence of preda­tors (Smuts et al., 1987).

Com­mu­ni­ca­tion and Per­cep­tion

Food Habits

Fruit is the main food and is gen­er­ally pref­ered over other avail­able foods. C. alb­ifrons oc­ca­sion­ally eats in­sects or other small in­ver­te­brates. Ac­cord­ing to a year-long study in Peru's Manu Na­tional Park, white-fronted ca­puchins only seek out in­ver­te­brates when trav­el­ing to fruit­ing trees, or when droughts re­duce fruit avail­abil­ity. Other food sources in times of drought in­clude palm nuts, figs, and nec­tar. (Ter­borgh, 1992).

  • Animal Foods
  • insects
  • Plant Foods
  • seeds, grains, and nuts
  • fruit
  • nectar

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

White-fronted ca­puchins help to dis­perse the seeds of fruits they eat in their feces. This may carry propag­ules to an area that might not nor­mally be reached, far from the perime­ter of the tree. (Ter­borgh, 1992).

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

None known, Cebus alb­ifrons do not raid human food crops.

Con­ser­va­tion Sta­tus

Be­cause they are re­stricted to rain­for­est habi­tats, pop­u­la­tions of C. alb­ifrons are threat­ened by habi­tat de­struc­tion due to log­ging and for­est clear­ing. They are not cur­rently en­dan­gered be­cause their habi­tats con­tinue to be fairly wide­spread and pop­u­la­tion num­bers re­main fairly high. White-fronted ca­puchins are also hunted for meat in some areas. While this hunt­ing is not ex­ces­sive and sim­ply main­tains the pop­u­la­tion at a slightly lower level, it is a po­ten­tial threat (Smuts et al., 1987).

Other Com­ments

The so­cial or­ga­ni­za­tion of the genus Cebus has been found to closely re­sem­ble that of old world mon­keys. A 1966 study has pro­posed that this is the re­sult of sim­i­lar diets and risk of pre­da­tion (Smuts, etal., 1987).

Con­trib­u­tors

Michelle Mijal (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor), Mu­seum of Zo­ol­ogy, Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

chemical

uses smells or other chemicals to communicate

dominance hierarchies

ranking system or pecking order among members of a long-term social group, where dominance status affects access to resources or mates

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

frugivore

an animal that mainly eats fruit

herbivore

An animal that eats mainly plants or parts of plants.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

rainforest

rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

Hill, W. 1960. Pri­mates, Com­par­a­tive Anatomy and Tax­on­omy, IV Ce­bidae Part A.. Lon­don: The Ed­in­burgh Uni­ver­sity Press.

Nowak, R. 1991. Walker's Mam­mals of the World. Bal­ti­more and Lon­don: The Johns Hop­kins Uni­ver­sity Press.

Smuts, B., D. Ch­eney, R. Sey­farth, R. Wrang­ham, T. Struh­saker. 1987. Pri­mate So­ci­eties. Chicago: The Uni­ver­sity of Chicago Press.

Ter­borgh, J. 1992. Di­ver­sity and the Trop­i­cal Rain­for­est. New York: Sci­en­tific Amer­i­can Li­brary.