Overview

Brief Summary

MammalMAP: Guinea baboon

Guinea baboons (Papio papio) are the least researched of all baboons, but this is what we know of these apparently gentle creatures.

Guinea baboons are the smallest among the baboon species, and weigh between 13 and 26 kg. Like other baboon species, males are much larger than females. They have beautiful reddish-brown coats, with great variation in different parts, with the baboons in the west having lighter, strikingly red fur and the ones in east darker and more brownish fur. Interestingly, Guinea baboons have the same colour pelage on their backs, arms, cheeks and abdomen, something that does not occur in other baboons, although the skin on their face is purple black, and their bums pink. Males also have manes, although it is not as distinct as the manes of hamadryas.

Guinea baboons can be found in western equatorial Africa, in parts of Guinea, Guinea-Bissau and Senegal. Some have also been found in Mauritania and Mali. They prefer savannah, woodlands and Sahelian steppe, but also inhabit forests.

Papio papio eat a variety of plants, including roots, seeds, fruit, tubers and flowers, but would occasionally eat invertebrates as well as vertebrates if available. Researchers have also recently discovered that Guinea baboons enter caves to lick the walls, possibly to obtain essential salt.

These baboons seem to be the least aggressive of the species, and rather than using aggression, male baboons herd the troop using a combination of shaking, jumping and prancing to change the direction, as well as running to speed up the movement.

Guinea baboons sleep in large trees as night to avoid predators, some of which so large that the only way to access them is by leaping from cliffs or nearby trees. They also tend to sleep as far from the tree trunk as possible, rather than using the trunk of the tree to brace themselves like other baboons.

Something interesting about these baboons when facing danger: Apart from giving a volley of calls at night when predators approach, to alert predators of the presence of adult males, when predators are very close, the baboons will become nearly silent until the predator has passed the sleeping site. Clever baboons!

On the IUCN Red List, Papio papio is listed as Near Threatened, mainly because they have undergone widespread decline as a result of agricultural expansion, tree-felling as well as direct hunting for crop protection and as bush meat. Once again, humans seem to be the biggest threat of all.

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  • Oates, J.F., Gippoliti, S. & Groves, C.P. 2008. Papio papio. In: IUCN 2012. IUCN Red List of Threatened Species. Version 2012.2. . Accessed 12 June 2013
  • Shefferly, N. 2004. Papio papio. In: Animal Diversity Web. . Accessed 12 June 2013
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Distribution

Range Description

This west African species ranges from southern Mauritania and Mali to Guinea and north-western Sierra Leone (see Grubb et al. 1998 for discussion about occurrence in this country). Along its eastern limits, the Guinea baboon may be hybridising with the larger Olive Baboon Papio anubis.
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Geographic Range

Papio papio is found in a small portion of western equatorial Africa. These animals are found in parts of Guinea, Guinea-Bissau, and Senegal, with some popuations known in Mauretania and Mali.

This species is part of a complex of closely related African baboon species. We have an account of the whole genus under Papio.

Biogeographic Regions: ethiopian (Native )

  • Groves, C. 2001. Primate Taxonomy. Washington, D.C.: Smithsonian Insitution Press.
  • Anderson, J., W. McGrew. 1984. Guinea baboons (Papio papio) at a sleeping site. American Journal of Primatology, 6: 1-14.
  • Byrne, R. 1981. Distance vocalisations of guinea baboons (Papio papio) in Senegal: An analysis of function. Behaviour, 78: 283-313.
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Physical Description

Morphology

Physical Description

Guinea baboons are considered small among their congeners. Although measurements for this species are not reported, they can be assumed to be on the small end of those reported by Nowak (1999) for all non-hamadryas baboons. For these, head and body length ranges between 508 and 1,143 mm, with the tail adding an additional 456 to 711 mm to the total length. Weights range between 13 and 26 kg, with males significantly larger and heavier than females.

The pelage of P. papio is a reddish brown, with significant geographic variation. Those animals in the western portion of the range are lighter and more strikingly red than those found in the eastern portion of the range, where animals are darker and more brownish. Unlike many baboon species, P. papio characteristically display the same color pelage on back, arms, cheeks and abdomen. Individual hairs have multiple bands of color, and are wavey in texture. In other species of Papio, the youngest animals display a charateristic natal pelage, which differs from adult pelage in color and texture. Although the natal pelage of P. papio has not been reported, it can be assumed that infants display some differences from adults.

Like anubis and hamadryas baboons, Guinea baboon males have a mane, although the mane in this species is not as pronounced as it is in hamadryas baboon males.

The facial skin of P. papio is purple-black. The moderate amount of unfurred skin visible around the anal area of males is pinkish in color. The female ano-genital skin changes color depending upon reproductive condition and age, as detailed in the reproductive section of this account.

Papio papio has a medium-sized skull for the genus, and a normal facial orientation. The long face has a prominent muzzel. Adults have 32 teeth. Canine teeth are large, especially in males, and the first lower premolar has been modified to serve as a hone for the upper canine. The large molars are strongly bilophidont.

Range mass: 13 to 26 kg.

Range length: 508 to 1143 mm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger; ornamentation

  • Napier, J., P. Napier. 1985. The natural history of the primates. Cambridge, Massachusetts: The MIT Press.
  • Nowak, R. 1999. Walker's Mammals of the World, Sixth Edition. Baltimore: The Johns Hopkins University Press.
  • Happel, R. 1988. Seed-eating by West-African Cercopithecines, with reference to the possible evolution of bilophodont molars. American Journal of Physical Anthropology, 75: 303-327.
  • Jolly, C. 1993. Species, subspecies, and baboon systematics. Pp. 67-107 in W Kimbel, L Martin, eds. Species, Species Concepts, and Primate Evolution. New York: Plenum Publishing.
  • Harvey, P., R. Martin, T. Clutton-Brock. 1987. Life histories in comparative perspective. Pp. 181-196 in B Smuts, D Cheney, R Seyfarth, R Wrangham, T Struhsaker, eds. Primate Societies. Chicago: The University of Chicago Press.
  • Gauthier, C. 1999. Reproductive parameters and paracallosal skin color changes in captive female Guinea baboons, Papio papio.. American Journal of Primatology, 67: 74.
  • Primate Info Net, 2002. "Primate Info Net" (On-line). Guinea Baboon (Papio papio). Accessed July 14, 2003 at http://www.primate.wisc.edu/pin/factsheets/papio_paio.
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
This species inhabits woodlands, savanna, and Sahelian steppe within reach of water. It also inhabits gallery forests and secondary forest in the south of its range. Rich food resources and good protection in the Niokolo Koba National Park in Senegal allow large aggregations of harem groups, numbering 10-200 (sometimes >500) individuals, to forage together. Guinea Baboons eat seeds, shoots, roots, fruits, fungi, invertebrates, small vertebrates, and eggs. Where agriculture has expanded, rice, maize, yams, groundnuts, and other cultivated crops are also taken.

Systems
  • Terrestrial
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There are few reports regarding the habitat of this species. Guinea baboons have only been studied extensively in one location, the Parc National du Niokolo-Koba in eastern Senegal. This park is located at the border of Sudan-type savanna and Guinea-type savanna.

The Mont Assirik area of the Parc, where P. papio has been studied, is topographically complex. Steep sided valleys radiate from Mont Assirik. Thin stripss of gallery forest are found along the seasonal watercourses, but comprize less than 5% of the available habitat. There are some permanent water pools located deep in these valleys.

In addition to gallery forest, vegetative cover in the area includes both deciduous woodland and bamboo (42%), with the remainder of the land covered by non-wood vegetation. These non-wooded areas vary seasonally, sometimes having very tall grasses, and at other times of the year being burned to the ground, creating very bare, open habitat.

Habitat Regions: tropical

Terrestrial Biomes: savanna or grassland ; forest ; rainforest

Other Habitat Features: agricultural

  • Dunbar, R., M. Nathan. 1972. Social organization of the Guinea baboon, Papio papio . Folia Primatologica, 17: 321-334.
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Trophic Strategy

Food Habits

Baboons are omnivorous primates, subsisting often on roots, tubers, bulbs and corms of grasses. They will eat meat when it is available.

In a study of captive animals, various fruits were presented to a Guinea baboon, and the portion of the fruit eaten was recorded. The animal was most inclined to eat the seeds of these fruits, although other portions of fruits, such as the pericarp and the flesh, were also consumed.

When processing seeds to eat, the Guinea baboon and other Cercopithecine monkeys tested used their molars to puncture and then to crush the seeds. Researchers think that this may indicate that the strongly bilophodont molars of cercopithecine primates may be an adaptation to seed predation.

Animal Foods: birds; mammals; eggs; insects

Plant Foods: leaves; roots and tubers; seeds, grains, and nuts; fruit; flowers

Primary Diet: omnivore

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Associations

Ecosystem Roles

Guinea baboons probably play a role in soil aeration through the digging of corms, roots, and tubers. They are likely to disperse the seeds of the fruits and grains that they eat. Baboons provide food for their predators, may impact populations of small animals on which they sometimes feed.

Ecosystem Impact: disperses seeds; soil aeration

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Predation

Specific details on predation of Guinea baboons are not available. However, large African carnivores, such as African wild dogs, lions, leopards, and hyaenas are sympatric. These are presumed to prey upon the baboons.

Guinea baboons appear to have two strategies to avoid predation. When presumed predators are noted at night, adult male baboons will begin to call in protracted nocturnal volleys. These calls may alert the predators to the presence of the adult males, thereby warning them from a risky attack on a sleeping group of baboons. When predators are very close, the baboons appear to rely on crypsis, becoming nearly silent until the predator has passed the sleeping site.

In addition to their vocalizations toward predators, Guinea baboons are known to sleep in very large trees, which might be difficult for predators to access. Indeed, the baboons themselves have some difficulty reaching their sleeping sites, often propelling themselves into the crown of the sleeping tree from the branches of smaller trees. Use of such sleeping sites itself could be considered a behavior which thwarts predators.

Known Predators:

  • McGrew, W., C. Tutin, D. Colins, S. File. 1989. Intestinal parasites of sympatric Pan trogolodytes and Papio Spp. at two sites: Gombe (Tanzania) and Mt. Assirik (Senegal). American Journal of Primatology, 17: 147-155.
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Known prey organisms

Papio papio preys on:
Insecta
Aves
Mammalia

This list may not be complete but is based on published studies.
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Known predators

Papio papio is prey of:
Panthera leo
Panthera pardus
Lycaon pictus
Crocuta crocuta
Hyaena hyaena

This list may not be complete but is based on published studies.
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Life History and Behavior

Behavior

Communication and Perception

Guinea baboons are highly communicative animals. They communicate with one another using a variety of vocalizations and physcial interactions. In addition to vocalizations to one another, these animals have vocal communications apparently intended to be received and interpreted by predators.

In Senegal, Guinea baboons are especially vocal. Their high rate of calling provides researchers with an excellent opportunity to test the function of various vocalizations.

Among the vocalizations made by P. papio are several loud calls, which can be heard at great distance, as well as some softer calls, generally used in more intimate contexts. What follows is a summary of different types of calls and the animals within the troop who make them.

All age and sex classes except infants give a loud call known as a wahoo bark. Adult males have a sterotyped version of this call, sometimes called a Type 2 loud call. In addition to this loud call, there are sharp barks--explosive single phrased calls given by all individuals except infants. Adult males are known to make Type 1 loud calls, or roar-grunts. These consist of a low hum, followed by a series of loud, deep grunts, which become lower in pitch and further apart as the series of grunts progresses.

In addition to loud calls, Guinea baboons are known to make several types of grunting vocalizations. Deep grunts, which are apparently given only by adult males, are long, low grunts, which have fluctuating pitch and volume. Rapid grunts, given by all animals except infants, are a quick, continuous series of grunts. Two-phase grunts are produced on both inhalation and exhalation. Two-phased grunts are loud, and are made in a rapid series by all animals except infants. Finally, copulation grunts are given by estrus females after copulation. These vocalizations consist of a loud grunt followed by a series of more quiet grunts.

A vocalization called a geck is given by all age and sex classes, including infants. Gecks are brief, sharp vocalizations which are given either in a rapid series or singly. Infants make a sheeplike moan, starting low and rising in pitch.

The fuctions of these calls has been analyzed by examining the context and habitats in which they are given. Three main sorts of contexts of calling are evident for Guinea baboons: Nocturnal volleys, intergroup coordination, and agonistic disturbances.

During the night, nocturnal volleys of adult male loud calls are apparently provoked by the sounds of predators such as lions, leopards, and hyaenas, or by the sound of other baboon groups making such nocturnal calls. Chains of volleys ring through the forest, in an apparent chain reaction to an initial stimulus. These volleys include type 1 and type 2 loud calls. The baboons making the calls do not move from their sleeping sites.

One possible function for nocturnal volleys is that the calls are designed to advertize to predators the number of adult male baboons present in a sleeping site, possibly indicating the strength of the defense against a predator which the group could muster. However, in one observation a lion approached a Guinea baboon sleeping site, passing directly below the tree where the baboons were reposing. As the lion approached, the volley of calls gradually decreased until the baboons were silent. The calls increased again as the lion moved away. This may indicate either that the baboons were too afraid to keep up their calls when in close proximity to the predator, or that the strategy of deterence had failed, and so the baboons were reduced to a secondary strategy of remaining cryptic, hoping the predator would pass them by.

Vocalizations are also used in coordinating group movements. Double-phase barks, type 2 loud calls, and single phase barks all increased in frequency when a group was undergoing fission, fusion, or passing by another group. Such increased calling rates may help baboons to avoid separation in thick vegetation. When separated, peaks of barking may help the animals maintain contact so that subgroups can rejoin one another.

Because of the high density of baboons in the area of study near Mont Assirik, groups of baboons frequently encounter one another during the course of the day. Sometimes these groups will fuse. Groups known to have slept in different locations are known to occasionally fuse, and so calls may be an important means by which different groups identify one another.

Papio papio tends to feed in small groups of 5 to 10 animals while using areas of tall grass. In other habitats, baboons typically take pains to maintain much larger group sizes. When the baboons are done using tall grass habitat, the foraging parties regroup efficiently, using bark calls to coordinate the reunion.

The final major context of calls is during agonistic disturbances. During intragroup agonism, wahoo and sharp barks cluster with screams and gecks. These latter calls are associated with submission and fear. Rapid grunting is also common in this context, and may be associated with branch-shaking displays, attacks, and threats. Roargrunts, or type 1 loud calls, are often given after aggression.

In addition to this impressive array of vocal communications, P. papio exhibits tactile communication. Grooming is common in all primates, and is an apparent indicator of social bonds between individuals. Various forms of touching are also important in greetings, with mounting, presenting of the rump, and even touching of the genitals sometimes plays a role. The intensity of these greetings is associated with the bond between individuals.

Although not reported for Guinea baboons, some chemical communication is known to occur in other species of Papio. Female baboons are known to produce aliphatic acids when they are in estrous, apparently enhancing their sexual attractiveness to males. It is possible that Guinea baboon females produce similar scent cues.

Communication Channels: visual ; tactile ; acoustic

Perception Channels: visual ; acoustic

  • Hrdy, S., P. Whitten. 1987. Patterning of sexual activity. Pp. 370-384 in B Smuts, D Cheney, R Seyfarth, R Wrangham, T Struhsaker, eds. Primate Socieities. Chicago: The University of Chicago PRess.
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Life Expectancy

Lifespan/Longevity

The lifespan for P. papio is not known. However, P. hamadryas has an average lifespan around 35 years, and a maximum measured lifespan in captivity of 45 years. It is likely that Guinea baboons are similar.

Average lifespan

Status: captivity:
40.0 years.

Average lifespan

Sex: male

Status: captivity:
27.0 years.

Average lifespan

Status: captivity:
25.8 years.

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Reproduction

P. papio is the most poorly known of all the Papio species. Perhaps because the habitat of Guinea baboons allows poor visibility, much is unknown about these monkeys.

The social organization of P. papio appears to be multi-leveled,  much like that of hamadryas baboons. The basic unit of social  organization is the OMU, or One Male Unit, comprized of a single adult  male, adult females, juveniles, and sometimes subadult males. These  OMUs may aggregate into higher order associations for travel  through areas where there is a high risk of predation, and at sleeping  sites. Unlike males of P. hamadryas, male Guinea baboons do not  aggressively "herd" their females, although males do control the  movements of the groups.

Although it has been proposed that adult males may be able to restrict the sexual access which other males have to females in their OMUs, multiple males, both adult and subadult, have been observed to mate with the same female. In these observations, adult males were reported to be uncompetitive and apparently tolerant of one another.

If such noncompetitive, polygynadrous mating is the rule in this species, P. papio would be an outlier within the genus. Most baboons can be characterized as exhibiting a great deal of intermale competition for access to reproductive females. In other baboons, this competition results either in the formation of single male harem units, as is the case with hamadryas baboons, or temporary consortships between males and estrous females, during which the male maintains exclusive reproductive access to the female, as commonly seen in the other species of baboons.

It should be noted that the observations of Guinea baboons mating occurred while the baboons were in their sleeping trees (Dunbar and Nathan, 1972). These trees tend to be very tall, and, as there is a real risk of dying as a result of a fall, it may be that the location of the observed copulations, rather than the especial tolerance of the males, may be responsible for the lack of competition seen between males in that study. Further, it is not clear from the reports of these matings whether the males who mated with the same female belonged to the same OMU. There are no data available regarding the extent to which sexual access to females may be restricted by the males or by the females themselves, as they approach ovulation. Further research on the mating behavior of P. papio would help to clarify the reproductive significance of the OMU.

Paucity of data regarding long-term relationships between individually identified Guinea baboons prevents speculation on how males or females choose their mates. In other species of baboons, subgroups within a troop are often formed for reproductive purposes, such as the OMUs seen in hamadryas baboons, or the consortships seen in anubis, yellow, and chacma baboons. If the OMU of Guinea baboons have reproductive significance, as is likely, it is not known what criteria females may use in joining one male versus another.

Mating System: polygynous ; polygynandrous (promiscuous)

There is virtually no information available for reproduction in this species. Harvey, Martin, and Clutton-Brock (1987) report that the gestation period for Guinea baboons is 184 days, and the interbirth interval is 423 days.

In captivity, females experience the first swelling of their sexual skin at a mean age of 3.8 years. The sexual swelling lasts for an average of 13.2 days. The female cycle length is 29.3 days. First pregnancy occurs at the mean age of 4.3 years. The timing of such events is typically accelerated in captive animals compared to their wild counterparts. There are no data available on the timing of reproductive maturity in males of this species, although in other baboons, males reach reproductive maturity around 60 to 74 months of age.

Females apparently advertize their sexual condition through changes in the color and shape of the skin surrounding the ano-genital region. The pink skin of the ano-genital region becomes swollen and rounded as the female approaches ovulation. This swelling typically lasts about 13.2 days. During the rest of the cycle, the skin in the ano-genital area is flat with a wrinked texture.

The skin surrounding the ischial callosities is black in young females, but during pregnancy can undergo rapid changes in color (termed a "color waltz") before settling into a permanent dark pink color. Older females tend to show a less pronounced "color waltz" at the beginning of pregnancy, and are more likely to have pink or dark pink skin surrounding their ischial callosities at times other than during pregnancy.

Although no data are available for P. papio, anubis baboons (P. anubis) wean their young around 420 days of age. Young of other baboon species become independent sometime after weaning, although the mother may continue to carry, groom, and otherwise help her offspring after that time. It is reasonable to assume that the same is true of Guinea baboons.

In other species of baboons, there are specific patterns of dispersal of males and females which are important in structuring the social system. For example, in hamadryas baboons, females leave their natal groups and each becomes part of a social unit controlled by a single adult male. In yellow and olive baboons, females remain in their natal groups for life and maintain long-term bonds with their female kin. The social stucture of the group revolves around the kin relationships of the females, with particular matrilines holding stable positions in a dominance heirarchy. In these species, male baboons emigrate into new social groups, and must establish themselves in the dominance heriarchy of those groups.

It is not known whether P. papio is a male-transfer or a female-transfer species, just as it is not known whether there is a stable female core to Guinea baboon OMUs. The stability of OMUs through time has not been examined, and the kin relationships between males whose OMUs associate with one another are not known. Further research on the emigration patterns of these baboons would help to clarify a great deal about the social structure and reproductive behavior of this species.

Breeding interval: Although the breeding interval of Guinea baboons has not been reported, it is probably like other baboons, with females producing young every 1.5 to 2 years.

Breeding season: Most baboon species are capable of reproducing throughout the year.

Average number of offspring: 1.

Average gestation period: 184 days.

Average age at sexual or reproductive maturity (female): 4.3 years.

Key Reproductive Features: iteroparous ; year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); fertilization ; viviparous

Little is known about the parental care exhibited by this species. However, in other baboons, the mother performs the bulk of parental care. This parental care is substantial, as the young baboon cannot walk or climb on its own. The mother grooms her offspring, carries it, and provides it with nourishing milk. The age of weaning for P. anubis is around 420 days, and it is likely that P. papio is similar.

In other baboon species, males play some role in parental care. In hamadryas baboons, where only one male mates with the females in the social group, the father sometimes holds, carries, or shares meat with his offspring. In other species of baboon, males respond to some infants within the troop in a similar fashion. These infants are usually the offspring of females with whom the male has a long-term friendship, and are therefore likely to be be the offspring of the male. Adult males and infants in P. papio have been observed to associate with one another, with the OMU leader sometimes carrying and grooming the infants and juveniles of his OMU. It is not known at this time whether the OMU leader is the likely father of these offspring.

Because the social system of these animals is still poorly understood, it is not known whether animals continue to associate with parents of either sex after independence. In P. hamadryas, adult male relatives have life-long associations. In P. anubis, P. cynocephalus, and P. ursinus, females are known to interact with their female kin throughout their lives. In these latter species, females inherit a dominance rank immediately below that of their mother. Further research on the social structure of P. papio will allow assessment of the inheritance of rank in this species, and help to clarify questions regarding the extent of parental care in this species.

Parental Investment: altricial ; pre-fertilization (Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Male, Female); pre-independence (Provisioning: Female, Protecting: Male, Female); extended period of juvenile learning

  • Nowak, R. 1999. Walker's Mammals of the World, Sixth Edition. Baltimore: The Johns Hopkins University Press.
  • Altmann, J. 1980. Baboon Mothers and Infants. Chicago: The University of Chicago Press.
  • Stein, D. 1984. The Sociobiology of Adult Male and Infant Baboons. Norwood, NJ: Ablex Publishing.
  • Melnick, D., M. Pearl. 1987. Cercopithecines in multimale groups: Genetic diversity and population structure. Pp. 121-134 in B Smuts, D Cheney, R Seyfarth, R Wrangham, T Struhsaker, eds. Primate Societies. Chicago: The University of Chicago Press.
  • Pusey, A., C. Packer. 1987. Dispersal and philopatry. Pp. 250-266 in B Smuts, D Cheney, R Seyfarth, R Wrangham, T Struhsaker, eds. Primate Societies. Chicago: The University of Chicago Press.
  • Smuts, B. 1987. Sexual competition and mate choice. Pp. 385-399 in B Smuts, D Cheney, R Seyfarth, R Wrangham, T Struhsaker, eds. Primate Societies. Chicago: The University of Chicago Press.
  • Harvey, P., R. Martin, T. Clutton-Brock. 1987. Life histories in comparative perspective. Pp. 181-196 in B Smuts, D Cheney, R Seyfarth, R Wrangham, T Struhsaker, eds. Primate Societies. Chicago: The University of Chicago Press.
  • Anderson, J., W. McGrew. 1984. Guinea baboons (Papio papio) at a sleeping site. American Journal of Primatology, 6: 1-14.
  • Boese, G. 1973. Social behavior and ecological considerations of West African baboons (Papio papio). Pp. 205-230 in R Tuttle, ed. Socioecology and Psychology of Primates. The Hague: Mouton.
  • Byrne, R. 1981. Distance vocalisations of guinea baboons (Papio papio) in Senegal: An analysis of function. Behaviour, 78: 283-313.
  • Dunbar, R., M. Nathan. 1972. Social organization of the Guinea baboon, Papio papio . Folia Primatologica, 17: 321-334.
  • Galat-Luong, A., G. Galat, S. Hagell. In Press. Social organization and reproductive strategies in Guinea Baboons (Papio hamadryas papio). L Swedell, S Leigh, eds. Baboons: Behavioral, Ecological, and Life History Perspectives. Kluwer Academic Publishers.
  • Gauthier, C. 1999. Reproductive parameters and paracallosal skin color changes in captive female Guinea baboons, Papio papio.. American Journal of Primatology, 67: 74.
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Molecular Biology and Genetics

Molecular Biology

Barcode data: Papio papio

The following is a representative barcode sequence, the centroid of all available sequences for this species.


There are 3 barcode sequences available from BOLD and GenBank.  Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.  See the BOLD taxonomy browser for more complete information about this specimen and other sequences.

ATTGGGACTTTATACCTATTATTTGGTGCATGAGCCGGAGTTACAGGCATGGCCCTA---AGTCTTCTCATTCGAGCCGAACTGGGCCAACCCGGTAGCCTACTAGGCAAT---GATCACATCTACAACGTCATTGTAACGGCCCATGCGTTCGTCATAATCTTTTTCATGGTTATACCTATTATAATTGGAGGCTTCGGAAATTGGTTGGTACCTCTAATA---ATTGGCGCTCCTGACATAGCATTCCCCCGTTTAAACAACATAAGTTTCTGACTCCTTCCCCCTTCTTTCCTGCTACTAATAGCATCAATCGCAGTAGAAGCCGGTGCTGGGACAGGTTGAACAGTGTATCCTCCTTTGTCAGGGAACTTCTCCCACCCGGGGGCCTCCGTAGACCTA---GTCATCTTCTCTCTTCACCTAGCGGGCATTTCCTCCATCCTAGGGGCCATCAACTTCATTACCACTATTATCAACATAAAACCCCCTGCAATATCCCAGTATCAAACCCCTTTATTTGTCTGATCGATCCTAATTACAGCGGTCCTCCTACTTCTCTCCCTACCAGTCCTAGCCGCC---GGCATCACTATACTATTAACAGATCGTAACCTCAATACTACTTTCTTCGACCCTGTCGGAGGAGGAGACCCTATTCTATACCAACAC
-- end --

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Statistics of barcoding coverage: Papio papio

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 3
Specimens with Barcodes: 3
Species With Barcodes: 1
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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
NT
Near Threatened

Red List Criteria

Version
3.1

Year Assessed
2008

Assessor/s
Oates, J.F., Gippoliti, S. & Groves, C.P.

Reviewer/s
Mittermeier, R.A. & Rylands, A.B. (Primate Red List Authority)

Contributor/s

Justification
Unlike other Papio species, there is reason to believe that Guinea Baboons have undergone a range contraction, in the face of large-scale agricultural expansion, persecution and hunting, possibly on the order of about 20-25% in the past 30 years. Their adaptability to a wide variety of habitats has probably enabled them to remain locally common in the areas where it occurs. Almost qualifies as threatened under criterion A2cd.

History
  • 1994
    Insufficiently Known
    (Groombridge 1994)
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IUCN lists Guinea baboons as lower risk/near threatened. Other agencies do no list this species. It is possible that taxonomic difficulties within the genus Papio are responsible for the failure of other agencies to list these baboons.

US Federal List: no special status

CITES: appendix ii

IUCN Red List of Threatened Species: near threatened

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Population

Population
They are reported to be common in many parts of their range (e.g., The Gambia and south-eastern Guinea-Bissau), and although patchily distributed even appear to be relatively abundant in a few places.

Population Trend
Unknown
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Threats

Major Threats
Outside the Niokolo-Koba National Park, this species has undergone widespread declines as a result of extensive agricultural expansion, tree-felling, and direct hunting for crop protection and for meat in Guinea. In the past, large numbers were exported for laboratory use, particularly in Senegal.
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Management

Conservation Actions

Conservation Actions
It is listed as Class B under the African Convention, and under Appendix II of CITES. This species is protected in the Niokolo-Koba National Park (Senegal), where densities of 2-15 individuals/km² have been estimated, and in Outamba-Kilimi National Park in Sierra Leone.
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

Guinea baboons are known to harbor the trematodes which cause schistisomiasis in humans. Although nothing has been specifically reported for Guinea baboons, other species of baboons are known to raid crops. Baboons are large animals, and they are known to bite to defend themselves if cornered.

Negative Impacts: injures humans (bites or stings, carries human disease); crop pest

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Economic Importance for Humans: Positive

Baboons are used extensively in medical and behavioral research. In addition, they are often housed in zoos, allowing many people to be entertained by their antics.

Positive Impacts: ecotourism ; research and education

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Wikipedia

Guinea baboon

The Guinea baboon (Papio papio) is a baboon from the Old World monkey family. Some (older) classifications list only two species in the genus Papio, this one and the hamadryas baboon. In those classifications, all other Papio species are considered subspecies of P. papio and the species is called the savanna baboon.

The Guinea baboon inhabits a small area in western Africa. Its range includes Guinea, Senegal, Gambia, southern Mauritania and western Mali. Its habitat includes dry forests, gallery forests, and adjoining bush savannas or steppes. It has reddish-brown hair, a hairless, dark-violet or black face with the typical dog-like muzzle, which is surrounded by a small mane, and a tail carried in a round arc. It also has limb modifications that allow it to walk long distances on the ground. The Guinea baboon is the smallest baboon species, weighing between 13 and 26 kg (28.6–57 lbs). Their life spans are between 35 and 45 years.

It is a diurnal and terrestrial animal, but sleeps in trees at night. The number of suitable sleeping trees limits the group size and the range. It lives in troops of up to 200 individuals, each with a set place in a hierarchy. Group living provides protection from predators such as the lion and various hyena species. Like all baboons, it is omnivorous, eating fruits, buds, roots, grasses, greens, seeds, tubers, leaves, nuts, cereals, insects, and small mammals. Because it eats almost anything available, it is able to occupy areas with few resources or harsh conditions. Its presence may help improve habitats because it digs for water and spreads seeds in its waste, encouraging plant growth.

The Guinea baboon is a highly communicative animal. It communicates by using a variety of vocalizations and physical interactions. In addition to vocalizations to each other, this animal has vocal communications apparently intended to be received and interpreted by predators.

Due to its small range and the loss of its habitat, the Guinea baboon is classified as "near threatened" by the IUCN.

Physical description[edit]

Baboon refers to the large-bodied primates with marked sexual dimorphism and having females and young that are dependent on males for protection.[3] Guinean baboons have a red tone to their fur, and are sometimes referred to as the red baboon. They lack hair on their hindquarters, and their faces are black with yellow-brown sideburns. Females' rumps are pink in color and males have a mane of fur around their heads and shoulders. A characteristic feature of baboons is their long molars and broad incisors. The long canines are evidence of sexual dimorphism in baboon species. Their forelimbs and hindlimbs are nearly equal in length and their digits on their hands and feet are relatively short and stout, making in difficult for them to climb.[4]

Baboons are one of the largest groups of monkeys and are sexually dimorphic is body size (meaning the males and females have differing body sizes).[4] They can range in weight from 13 and 26 kg (28–57 lbs), making them the smallest of the baboon species.

Habitat and distribution[edit]

Generally found in woodland savannas, they seasonally congregate near permanent water sources, breaking off in the wet season into smaller groups. Baboon species are all allopatric, but some of their ranges do overlap, and some interbreeding can occur.[4] These baboons are found in a wide range across Africa in savannah habitats. Its range includes Guinea, Senegal, Gambia, southern Mauritania and western Mali. Most typically they are in the forests and savannah of sub-Saharan Africa. They can also be found in grasslands, rain forests, and other open areas.[4]

Ecology[edit]

They are diurnal, living on the ground instead of the trees, and typically sleep in trees at the terminal ends of branches.[5] Their group size is widely variable and ranges from 40 to 200. However, the most common troop size is 30–40 individuals. Often, a pronounced male hierarchy and fierce competition for females happens within the group. This competition leads to sexual dimorphism among the species.[4] When it comes to feeding, they are independent foragers, and females are always paired with males when foraging so they can be protected. Females may chose to follow the same males from year to year.[3]

Diet[edit]

Guinean baboons eat a variety of foods, but their main sources of nutrients are fruits, roots, and tubers, but also grass seeds and leaves. This type of feeding is referred to as opportunistic faunivores. They have also been known to eat small mammals and invertebrates.[4]

Behavior[edit]

Socially, baboons live in harems, with one dominant male and one subordinate male with several females and juveniles. These groups are usually small, but join with larger groups to form a troop; these groups sleep or forage together. The Guinean troops are large multiple-male, multiple-female troops with 50–300 baboons. The harems consist of two to five females which mate with the dominant male.[6] Baboons are not very good climbers, so they spend the majority of their time foraging on the ground.[3] Guinean baboons forage along the ground during the day, but almost always climb trees or cliffs when sleeping. Guinea baboons run along the ground in a quadrupedal pattern.[4]

Communication[edit]

The Guinea baboons have a host of vocal, visual, and tactile communications. Their several vocal calls each convey different messages, and consist of predator warnings, signaling friendly intentions, submissive calls, and frustration vocalizations. Many of these calls can be used in combination with either each other or with some other form of visual or tactile communication. Visual communications serve many of the same purposes as the vocal calls, and are often accompanied by some sort of vocal call. Tactile communication is usually tied to visual communication and can range from mouth-to-mouth touching to biting or slapping.[7]

Reproduction[edit]

Guinea baboon females exhibit sexual swelling that begins about 10 to 12 days before it plateaus and remains consistent for about eight days. This is a good signal to males that the females are ready for sex. Females then participate in the social behavior of presenting, which is when she signals to the males in the group she is ready for copulation.[7]

The mean gestation period is about six months and nursing continues until about six to eight months.[7]

References[edit]

  1. ^ Groves, C. P. (2005). Wilson, D. E.; Reeder, D. M, eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. p. 167. OCLC 62265494. ISBN 0-801-88221-4. 
  2. ^ Oates, J. F., Gippoliti, S. & Groves, C. P. (2008). Papio papio. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 4 January 2009.
  3. ^ a b c Bramblett, C. (1994). Patterns of Primate Behavior. Waveland Press Inc. pp. 129–132. 
  4. ^ a b c d e f g Fleagle, J. (1988). Primate Adaptation & Evolution. Academic Press Inc. pp. 169–171. 
  5. ^ Anderson, J. (1998). "Sleep, Sleeping Sites, and Sleep-Related Activities: Awakening to Their Significance". American Journal of Primatology 43: 63–75. 
  6. ^ Maestripieri, D. (2005). "Female Copulation Cells in Guinea Baboons: Evidence for Postcopulatory Female Choice?". International Journal of Primatology 26 (4): 737–758. doi:10.1007/s10764-005-5306-6. 
  7. ^ a b c Dolhinow, P. (1972). Primate Patterns. Academic Press Inc. pp. 142–179. 
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