|Geographic range; currently the Tunisian population shown on the map is extinct.|
The Barbary macaque (Macaca sylvanus), Barbary ape, or magot is a species of macaque unique for its distribution outside of Asia and for its vestigial tail. Found in the Atlas Mountains of Algeria and Morocco and El-Kouf National Park in Libya along with a small population of unknown origin in Gibraltar, the Barbary macaque is one of the best-known Old World monkey species.
The Barbary macaque is of particular interest because males play an atypical role in rearing young. Despite uncertain paternity, males are integral to raising infants. Generally, Barbary macaques of all ages and sexes contribute in alloparental care of young.
Macaque diets consist primarily of plants and insects and they are found in a variety of habitats. Males live to a maximum of 25 years while females may live up to 30 years. Besides humans, they are the only free-living primates in Europe. Although the species is commonly referred to as the "Barbary ape", the Barbary macaque is actually a true monkey. Its name refers to the Barbary Coast of Northern Africa.
The monkey is yellowish-brown to grey with a lighter underside. The Barbary macaque has a body length of around 556.8mm in females and 634.3mm in males and mean body weight is reported to be 9.9±1.03 kg in females and around 14.5 kg in males. Its face is dark pink and its tail is vestigial, measuring anywhere from 4 to 22mm. Males often have a more prominent tail. The front limbs of this monkey are longer than its hind limbs. Females are smaller than males.
The Barbary macaque is mainly found in the Atlas and Rif Mountain ranges of Morocco and Algeria and Jebel Akhdar in Libya. It is the only species of macaque that is distributed outside of Asia. These animals can occupy a variety of habitats, such as cedar, fir, and oak forests, or grasslands, scrub, rocky ridges full of vegetation. Most Barbary macaques inhabit cedar forests currently, however, this could reflect the present habitat availability rather than a specific preference for this habitat.
The diet of a Barbary macaque consists of a mixture of plants and insect prey. M. sylvanus consume a large variety of gymnosperms and angiosperms. Almost every part of the plant is eaten, including flowers, fruits, seeds, seedlings, leaves, buds, bark, gum, stems, roots, bulbs, and corns. Common prey caught and consumed by Barbary macaques are snails, earthworms, scorpions, spiders, centipedes, millipedes, grasshoppers, termites, water striders, scale insects, beetles, butterflies, moths, ants, and even tadpoles.
The Barbary macaque is gregarious, forming mixed groups of several females and males. Troops can have 10 to 100 individuals and are matriarchal, with their hierarchy determined by lineage to the lead female. Unlike other macaques, the males participate in rearing the young. Males may spend a considerable amount of time playing with and grooming infants. In this way, a strong social bond is formed between males and juveniles, both the male's own offspring and those of others in the troop. This may be a result of selectivity on the part of the females, who may prefer highly parental males.
The mating season runs from November through March. The gestation period is 147 to 192 days, and females usually have only one offspring per pregnancy. Females rear twins in rare instances. Offspring reach maturity at three to four years of age, and may live for 20 years or more.
Grooming other Barbary macaques leads to lower stress levels for the individuals that do the grooming. While stress levels do not appear to be reduced in animals that are groomed, grooming more individuals leads to even lower stress levels; this is a benefit that might outweigh the costs to the groomer, which include less time to participate in other activities such as foraging. The mechanism for reducing stress may be explained by the social relationships (and support) that are formed by grooming.
Male Barbary macaques interfere in conflicts and form coalitions with other males, usually with related males rather than with unrelated males. These relationships suggest that males do so in order to indirectly increase their own fitness. Furthermore, males form coalitions with closely related kin more often than they do with distantly related kin. These coalitions are not permanent and may change frequently as male ranking within the group changes. Although males are more likely to form coalitions with males who have helped them in the past, this is not as important as relatedness in determining coalitions. Males avoid conflicting with higher ranking males and will more frequently form coalitions with the higher ranking male in a conflict. Close grouping of males occur when infant Barbary macaques are present. Interactions between males are commonly initiated when a male presents an infant macaque to an adult male who is not caring for an infant, or when an unattached male approaches males who are caring for infants. This behavior leads to a type of social buffering which reduces the number of antagonistic interactions among males in a group.
An open mouth display by the Barbary macaque is used most commonly by juvenile macaques as a sign of playfulness.
The main purpose of calls in Barbary macaques is to alert other group members to possible dangers such as predators. Barbary macaques can discriminate calls by individuals in their own group from those by individuals in other groups of conspecific macaques. Neither genetic variation nor habitat differences are likely causes of acoustic variation in the calls of different social groups. Instead, minor variations in acoustic structure among groups similar to the vocal accommodation seen in humans are the likely cause. However, acoustic characteristics such as pitch and loudness are varied based on the vocalizations of individuals they associate with, and social situations play a role in the acoustic structure of calls.
Barbary macaque females have the ability to recognize their own offspring’s calls through a variety of acoustic parameters. Mothers demonstrate different behaviors upon hearing the calls of other infant macaques as opposed to the calls of their own offspring. Because female macaques can distinguish among a variety of parameters, infant calls do not have to differ dramatically for mothers to be able to recognize their own infant’s call. More parameters for vocalizations lead to more reliable identification of calls in both infants and in adult macaques so it is not surprising that the same acoustic characteristics that are heard in infant calls are also heard in adult calls.
Although Barbary macaques are sexually active at all points during a female’s reproductive cycle, male Barbary macaques determine a female’s most fertile period by sexual swellings on the female. Mating is most common during a female’s most fertile period. The swelling size of the female reaches a maximum around the time of ovulation, suggesting that size helps a male predict when he should mate. This is further supported by the fact that male ejaculation peaks at the same time that female sexual swelling peaks. There is not a sufficient change in female sexual behavior around the time of ovulation in order to demonstrate to the male that the female is fertile. The swellings, therefore, appear necessary for predicting fertility.
Barbary macaque females differ from other non-human primates in that they often mate with a majority of the males in their social group. While females are active in choosing sexual associations, the mating behavior of macaque social groups is not entirely determined by female choice. These multiple matings by females decreases the certainty of paternity of male Barbary macaques and may lead them to care for all infants within the group. In order for a male to ensure his reproductive success, he must maximize his time spent around the females in the group during their fertile periods. Injuries to male macaques peaks during the fertile period which points to male-male competition as an important determinant of male reproductive success. Not allowing a female to mate with other males, however, would be costly to the male since doing so would not allow him to mate with more females.
Unlike other macaques where most parental care comes from the mother, Barbary macaques from all age and sex groups participate in alloparental care of infants. Male care of infants has been of particular interest to research because high levels of care from males is uncommon in groups where paternity is highly uncertain. Males even act as true alloparents of infant macaques by carrying them and caring for them for hours at a time as opposed to just demonstrating more casual interactions with the infants. Female social status plays a role in female alloparental interactions with infants. Higher ranking females have more interactions whereas younger, lower ranking females have less access to infants.
Interaction with the environment
Barbary macaques can cause major damage to the trees in their prime habitat, the Atlas Cedar forests in Morocco. Since deforestation in Morocco has become a major environmental problem in recent years, research has been conducted to determine the cause of the bark stripping behavior demonstrated by these macaques. Cedar trees are also vital to this population of Barbary macaques as an area with cedars can support a much higher density of macaques than one without them. A lack of a water source and exclusion of monkeys from water sources are major causes of cedar bark stripping behavior in Barbary macaques. Density of macaques, however, is less correlated with the behavior than the other causes considered.
The Barbary macaque was named by Carl Linnaeus in 1758, along with numerous other species named in that same year. The scientific name is Macaca sylvanus. Phylogenetic and molecular analysis with other primates has been done. Studies concerning interspecific DNA variation within the genus Macaca show that the Barbary macaque is most related to the Asian macaques. Scientists have also studied the Y-chromosome, however, this has been unfruitful. One study indicates that the Barbary macaque has origins in Morocco and Algeria. The results of a phylogenetic analysis show that M. sylvanus chromosomes resemble M. mnilatta with the exception of chromosomes 1, 4, 9, and 16. Relative to humans, M. sylvanus has a homolog of chromosome 13.
Relationship with humans
Wild populations of Barbary macaques have suffered a major decline in recent years to the point of being declared in 2009 as an endangered species by the IUCN. Three-quarters of the world population are located in the Middle Atlas Mountains.
This species is also poached for live specimens as pets in the illegal pet trade, and for clandestine collectors. Spain is the main entry point in Europe. Today, no accurate data exist on the location and number of individuals out of their habitat. An unknown number of individuals are included in zoological collections, at other institutions, in private hands, in storage, or waiting to be relocated to appropriate destinations.
The habitat of the Barbary macaque is under threat from increased logging activity. As such, they are listed as endangered by the IUCN Red List. Local farmers view the monkeys as pests, and engage in extermination of the species. Once common throughout northern Africa and southern Europe, only an estimated 12,000 to 21,000 Barbary macaques are left in Morocco and Algeria. Once, their distribution was much more extensive, reaching Tunisia and Libya. Their range is no longer continuous, with only isolated areas of range remaining. During the Pleistocene, this species inhabited the Mediterranean coasts and Europe, reaching Italy, Hungary, Spain, Portugal and France, and as far north as Germany and the British Isles. The species decreased with the arrival of the Ice Age, becoming extinct in the Iberian Peninsula 30,000 years ago.
The skull of a Barbary macaque was discovered during excavation in the 1970s at the pre-Christian Navan Fort in County Armagh, Northern Ireland. Carbon dating tests suggest it died there in the third century BC.
Tourists interact with wild monkeys in many places, tourists may be encouraged to feed, photograph and touch them. Tourism may aid conservation but may also stress the animals. Aggressive behaviour by tourists stressed the animals physiologically. Stress related hormones were found in their droppings. Other tourist actions made the monkeys uneasy without apparent physiological stress. Stress behaviour in Barbary macaques increased when humans got too close to them, touched them or even photographed them. When tourists got too close macaques were more aggressive and less friendly to each other. High tourist numbers are not a problem for the macaques provided tourists stay at a distance. Macaques that interacted with tourists had more parasites, possibly due to crowding at feeding sites. Macaques in contact with tourists further were fatter with less healthy fur than their counterparts that did not receive unhealthy food from humans. Guidelines are needed to avoid tourists stressing the animals unnecessarily. 
Many of the mistaken ideas about human anatomy contained in the writings of Galen are apparently due to his use of these animals, the only anthropoid available to him, in dissections. Strong cultural taboos of his time prevented his performing any actual dissections of human cadavers, even in his role as physician and teacher of physicians.
The last wild population in Europe is that of Gibraltar, which unlike that of North Africa, is thriving. Currently, there are around 230 individuals living on the Rock of Gibraltar, and they form groups of up to 75 and will occasionally enter towns.
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- ARKive - images and movies of the Barbary macaque (Macaca sylvanus)
- Chisholm, Hugh, ed. (1911). "Barbary Ape". Encyclopædia Britannica (11th ed.). Cambridge University Press.