Vulnerable (C. calvus), Least concern (C. melanocephalus)
Life span: >30 years (captive)
Total population: Unknown
Regions: Neotropical South America
Gestation: 6 months
Height: 41.4 to 45.6 cm (M), 38.9 to 44 cm (F)
Weight: 2.66 to 3.45 kg (M & F)
Species: C. calvus, C. melanocephalus
Subspecies: C. c. calvus, C. c. novaesi, C. c. rubicundus, C. c. ucayalii, C. m. melanocephalus, C. m. ouakary
Other names: uacari; C. calvus: bald uakari, bald-headed uacari, red uakari,
red-and-white uacari; witte oeakari (Dutch); ouakari chauve (French); cacajao,
cacayao, huapo colorado, huapo rojo, uacaries, uacari blanco (Spanish); skallig
kortsvansaparöd uakari, skallig uakari, vit uakari (Swedish); C. c. novaesi:
Novaes' bald-headed uacari; uacarí (Spanish); C. c. rubicundus: red bald-headed
uacari; mono ingles, uacarí-vermelho (Spanish); C. c. ucayalii: Ucayali
bald-headed uacari, Peruvian red uacari; C. melanocephalus: black uacari, black-headed uacari,
Humboldt's black-headed uacari; zwartkopoeakari (Dutch); ouakara à tête noire
(French); mono chucuto, uacari-bicó, uacarí-preto (Spanish); svart uakari,
svartansiktad kortsvansapa, svarthuvad uakari (Swedish).
While some authors list several additional subspecies of uakari, as per Groves
(2005), only four subspecies of C. calvus are considered here. C.
melanocephalus is sometimes divided into two subspecies, C. m. melanocephalus
and C. m. ouakary, and here both are considered at the subspecific level as per
Hershkovitz (1987) for the sake of simplicity. Some authors also elevate the two subspecies of C.
melanocephalus to full species level, however here they are not treated as such.
In 2008, two additional species of uakari, C. ayresi (Aracá uakari) and
C. hosomi (Neblina uakari) were described (Boubli et al. 2008).
The common and generic names of the uakari species likely have their origin in
indigenous Amazonian languages (Barnett 2004).
Cacajao calvus rubicundus
Photo: Roy Fontaine
Medium-sized uakaris are the largest of the New World monkeys without a
prehensile tail and are characterized by the presence of a short and bushy tail
which is less than half to only one third of the head and body length of the
animal (Fontaine 1981; Hershkovitz 1987; da Cunha & Barnett 1989; Barnett
2005; Norconk 2007). The muzzle is broad (Hershkovitz 1987). The main
distinguishing characteristics between the two species of uakari are the head
and the pelage. The C. calvus head ranges from bald to sparsely
haired, while C. melanocephalus has plenty of hair (Barnett 2005). The
profound lack or near lack of pigment in the face and head of C. calvus
results in a reddish appearance of the face and head caused by the presence
blood vessels near the surface of the skin (Hershkovitz 1987; Barnett 2005).
The face of C. melanocephalus is black, and the head has blackish hair
(Hershkovitz 1987; Barnett 2005). The pelage of C. melanocephalus is generally
a rich and bright reddish-brown, with black head, neck, hands, and feet, while
C. calvus can range among subspecies from reddish to orange and buffy to whitish
or pale yellow (Hershkovitz 1987; Barnett 2005; A. Barnett pers. comm). C. m.
ouakary has a gold-colored cape and C. m. melanocephalus has a black one (A.
Barnett pers. comm.). The color differences between populations can be
arranged on a geographic continuum; that is, they grade from one to another by location
(Barnett 2005). This is well exhibited in C. calvus, where C. c. calvus is very
pale, while C. c. novaesi is orange-buff, C. c. rubicundus is reddish, and C. c.
ucayalii is reddish-orange (Hershkovitz 1987; Barnett & Brandon-Jones 1997).
Photo: Luiz Claudio Marigo
The ventrum is nearly bare (Barnett 2005). Both sexes have a sternal gland
which might be involved in olfactory communication (Fontaine & DuMond 1977).
In both species, the fur on the shoulders and anterior back is long, shortening
by the midback, and in C. melanocephalus, the hair on the sides of the
body can be up to 10 cm (3.9 in) long (Hershkovitz 1987; Barnett 2005). In
general, in both species, males are larger and weigh more than the females but
there are no differences in the pelage between males and females (Hershkovitz
1987; Barnett & Brandon-Jones 1997).
C. melanocephalus head and body lengths average 41.4 cm (16.3 in)
(male) and 38.9 cm (15.3 in) (female), while C. calvus average 45.6 cm
(18.0 in) (male) and 44.0 cm (17.3 in) (female) (Hershkovitz 1987). Based on
very small samples, male C. melanocephalus can weigh between 2.66 kg
and 2.8 kg (5.9 and 6.2 lb), while C. calvus of both sexes can weigh
between 2.75 and 3.45 kg (6.1 and 7.6 lb) (Ayres 1986 cited in Hershkovitz
Uakaris are predominantly arboreal quadrupeds, most frequently walking,
running, clamber-running, leaping and bridging in the upper and middle-upper
levels of the forest canopy (Walker 1996; Walker & Ayres 1996; Boubli 1997a;
Barnett 2005). Less frequently, arm-swinging is used, and on rare occasions,
bipedal movement is seen (Boubli 1997a). In addition, uakaris will often leap
or drop between supports during travel, a result of their relatively
discontinuous forest habitat (Walker 1996; Walker & Ayres 1996; Boubli
1997a). While feeding, uakaris usually sit and while resting they will either
sit or lie on their belly (Walker 1996). Uakaris are capable of swimming
(Barnett 2008). Uakaris seasonally forage on the ground (Ayres 1986; Barnett 2008).
In captivity, uakaris have lived into their mid-thirties (Weigl 2005).
CURRENT RANGE MAPS (IUCN REDLIST):Cacajao calvus
| Cacajao melanocephalus
Generally, uakaris are found in neotropical Amazonia, including Brazil,
Colombia, Peru, and Venezuela (Hershkovitz 1987; Boubli 1997a). Between the
species, C. melanocephalus is found in the Rio Negro basin area in the
Amazon region in far northwest Brazil, eastern Colombia and southern Venezuela
(Boubli 1993; 1997; Barnett 2005). C. calvus and its subspecies are
only found in Brazil and Peru but may have been present in Colombia until the
last century (Defler 2004). Among the subspecies of C. calvus, C.
calvus ucayalii is only found in northeastern Peru, confined to the south
by the Sheshea River, to the north and west by the Amazon River and Ucayali
River respectively, and in the east by the Yavari River (Aquino 1988; Heymann
1992; Ward & Chism 2003). C. c. rubicundus is restricted to the
area around the mouth of the Japurá River (Barnett & Brandon-Jones
1997). C. c. novaesi is only found in a restricted area along the Juruá River,
but probably has a wider distribution that needs further exploration (Barnett &
Brandon-Jones 1997). C. c. calvus has a limited distribution between
the lower Japurá and the Solimões and west to the
Auatí-Paraná (Barnett & Brandon-Jones 1997; Silva Jr. &
Martins 1999). However, it must be stressed that in many ways these
distributions are preliminary, sometimes require confirmation, and likely will
be expanded or changed with further research (see Barnett & Brandon-Jones
1997). An example of this is the discovery of a white uakari with pelage
similar in appearance to C. c. calvus, some 700 km (434.0 mi) from its
expected distribution (Silva Jr. & Martins 1999).
Uakaris are extremely hard to maintain in captivity, a fact reflected by
their low numbers in zoos and in the difficulty breeding captive individuals
(Whitehead 1984; http://www.isis.org).
In general, uakaris are found close to or in flooded or riparian forests
(Barnett & Brandon-Jones 1997). The habitats of the two species of uakari
can be roughly separated by the types of rivers with which their habitat is
associated. C. calvus, is found in habitats associated with
"white-water rivers" while C. melanocephalus is found in
habitats associated with "black-water rivers" (Ayres 1989; Barnett
& Brandon-Jones 1997). This is not a rule however, as C. calvus
has been seen around 60 km (37.3 mi) from any "white-water rivers"
(Peres 1997). The habitat types and floodplains associated with the two
different types of river have different features such as soil mineral content
and richness and the primary floodplain habitats can generally be divided into
two types várzea
(associated with white-water rivers) and igapó
(associated with black-water rivers) (Ayres 1989). Further, flooded forests of
the Amazon exhibit profound changes in water level between the seasons. An
example of this is at one study site, roughly 1200 miles (9131.2 km) west of
Manaus, Brazil, where várzea water levels are 40 feet (12.2m) higher
between March and August than they are during the rest of the year (Ayres 1990).
However, uakaris can be found in several types of habitat, including flooded
and unflooded igapó and várzea, swamp forest, various white sand
soil forests, floodplains, terra firme forest near igapó and
várzea, and transitional zones between flooded and terra firme forest
(Ayres & Johns 1987; Ayres 1989; Boubli 1997b; Peres 1997; Aquino 1998;
Defler 1999; Barnett et al. 2005a).
Some researchers suppose that uakaris are flooded-forest specialists while
others comment that some or even most of their time is spent in terra firme
forests and other habitat types (Ayres 1986 cited in Leonard & Bennett 1995;
Leonard & Bennett 1995; Boubli 1997a; Aquino 1998). Either way, uakaris are
not restricted to flooded or swamp forests (Bartecki & Heyman 1987). These
other habitat types can be a good distance from water, sometimes 2 km (1.2 mi)
from a river (Aquino 1998). In some cases, uakaris can be found in mountainous
areas and sometimes range up to 1500m (Boubli 1994; 1997b). There appears to be
some seasonal movement between habitats, with uakaris moving to flooded areas
during periods of fruit abundance and preferring terra firme or other habitat
types when more fruit is available outside of flooded forest (see Barnett &
Brandon-Jones 1997; Barnett et al. 2005 for discussion and review). However, when restricted by
geography, such a pattern is not seen (as is the case with C. c.
calvus) and some researchers suggest that the seasonal situation is more
complex than a simple bimodal model (Barnett & Brandon-Jones 1997; Barnett
& de Castilho 2000).
At one study site, at the Pico da Neblina National Park in Brazil,
rainfall averages 250-300 cm (98.4-118.1 in) per year and is almost evenly
distributed throughout the months, however in a regional sense, the first half
of the year is wetter than the second half. Temperature also varies little
throughout the year, averaging around 26°C (78.8°F) (Boubli 1997a).
C. melanocephalus are predominantly
but specialize in the seeds of hard-husked unripe
fruits. For C. melanocephalus, the recorded diet at one study site comprised of
89% fruits, 5% flowers, 4% leaves and leaf parts, and 2%
invertebrates (including ants, spiders, grasshoppers, katydids and roaches).
The concentration on unripe fruits is unlike any unlike other neotropical
frugivores, and is helped by special dentition and a chewing apparatus which
allows it to use foods which are unavailable to other primates (Ayres 1989;
1990; Boubli 1999). Up to 120
species of plant are exploited as food with a few preferred species making up a
significant proportion of the diet. The seeds of fruits are extremely important
in the diet, comprising the majority of fruit feeding observations (Boubli
1999). The majority of these come from unripe fruits. Fruits are often bitten
along their sutures, which require less force to puncture (Adrian Barnett pers. comm.).
Photo: Luiz Claudio Marigo
The known diets of C. calvus are similar to those recorded for
C. melanocephalus and C. ouakary, with
seeds of fruits predominating (67% of observations) followed by other parts of
fruit (10%), flowers (6%), nectar, some insects (5%) and unidentified foods (4%)
(Ayres & Johns 1987; Ayres 1989). Aquino & Encarnación (1999) noted C. c.
ucayalii eating 53 plant species from 20 families, of which 46% were consumed
for their seeds. Of these, 67% had thick heavy husks and were consumed in the
immature state. In the dry season, Peruvian red uakaris will also eat bromeliad
leaf bases, and also move to unflooded forest to feed on palm fruit as well as
(unspecified) flowers and leaves (Aquino & Encarnación 1994; Aquino 1995). For
C. ouakary, larvae of wasps and the eggs of turtles
are also reported as being eaten on occasion, with wasp nests raided by the
species (Barnett 1999; Barnett et al. 2005a; Barnett 2008). Almost one hundred species of
plant are eaten by C. calvus (Ayres 1989). Uakaris sometimes descend
to the ground during specific times of the year and forage for seeds and
seedlings (Ayres 1989; Barnett & de Castilho 2000; Barnett 2008). When
fruits are in short supply, leaves and pith are consumed (Barnett 2005; 2008). In addition,
during periods of relative fruit scarcity, uakaris will actually increase the
amount of ripe fruit pulp they consume because during periods of fruit
abundance, they will focus on unripe seeds and other abundant foods as preferred
resources (Boubli 1999).
Uakaris are diurnal.
The day of C. m. melanocephalus is spent
resting (22%), traveling (27%), feeding (20%), and moving/foraging (31%). Over
the course of the day, travel occurs most early and late in the day, resting
peaks in the late morning or early afternoon, feeding is relatively constant,
and moving/foraging is common in the morning and early afternoon (Boubli 1997a).
The white uakari (C. c. calvus) begins its day at sunup and descends from the
sleeping trees to feed. The troop will feed and move until noon with a period
of rest around midday. In the mid-afternoon, the troop will resume feeding and
moving and by dark, the group will have begun entering their sleeping site for
the night (Ayres 1990).
Uakaris are characterized by very large day ranges, traveling up to 4.4 km
(2.7 mi) or even 5 km (3.1 mi) per day during fruiting. Annual averages are
often lower; in one study with small sample sizes they averaged 2.3 km (1.4 mi)
per day (Ayres 1989; Boubli 1997a; 1999). They travel quickly (Boubli 1997b).
Some subspecies range even farther, with one estimate placing the day range of
C. c. ucayalii at an average of 7.3 km (4.5 mi) (Leonard & Bennett
1995; 1996). Ranging distances are dependent on the state of food availability
and during the high-water fruiting season distances traveled are farther than
during the dry season, when they are considerably shorter (Ayres 1990). Home
ranges of C. m. melanocephalus (minimum estimate of 10.53 km² (4.1 mi²))
are larger than those observed for C. calvus (5.0-5.5 km² (1.9-2.1
mi²)), but some estimates for C. c. ucayalii place home range at a very
large 30 km² (11.6 mi²) however, often the area within the home range that is
used the majority of the time is smaller, as is the case with C. calvus
(2.5-3.0 km² (1.0-1.2 mi²)) (Ayres 1989; Leonard & Bennett 1996; Boubli
Cacajao calvus calvus
Photo: Luiz Claudio Marigo
Harpy eagles (Harpya harpya) are a potential and actual predator of uakaris
(Leonard & Bennett 1996; Boubli 1997a; Barnett et al. 2005b). Other potential predators include
ocelots (Felis pardalis), tayras (Eira barbara) and Boa constrictor snakes.
Uakaris often react to perceived aerial threats, including bird species that are
not predators, such as toucans (Boubli 1997a).
In different locations, uakaris are sympatric with different primate species,
but across their distribution, they can be sympatric with members of the genera
(Leonard & Bennett 1996; Boubli 1999; 2002).
In some cases, uakaris are found in association with other primates including
spider monkeys (Ateles sp.), wooly monkeys (Lagothrix sp.), sakis (Chiropotes
sp. & Pithecia sp.), capuchins (Cebus sp.), and squirrel monkeys (Saimiri
sp.) (Leonard & Bennett 1996; Aquino 1988; 1998; Boubli 2002). Such
associations might provide predator protection and foraging benefits (Leonard
& Bennett 1996).
Competition for food comes from species with dietary overlap with uakaris,
such as macaws (Ara sp.), squirrels and sympatric primates such as squirrel
monkeys and capuchins. Such overlap and levels of potential competition require
quantitative assessment, but are probably low (Barnett 2005; Barnett et al.
2005a; Barnett 2008).
Sleeping occurs high in the trees, normally 17 (55.8 ft) to around 40 meters
(131.2 ft) up, with the troop distributed in different trees over about an acre,
with only 6-7 individual uakaris per sleeping tree (Ayres 1990; Aquino 1998).
Content last modified: July 21, 2008
Written by Kurt Gron. Reviewed by Adrian Barnett.
Cite this page as:
Gron KJ. 2008 July 21. Primate Factsheets: Uakari (Cacajao) Taxonomy, Morphology, & Ecology . <http://pin.primate.wisc.edu/factsheets/entry/uakari/taxon>. Accessed 2014 October 1.