|Female Barbary macaque with young|
|Geographic range; currently the Tunisian population shown on the map is extinct.|
The Barbary macaque (Macaca sylvanus), also known as Barbary ape or magot, is a species of macaque unique for its distribution outside Asia. Found in the Atlas Mountains of Algeria and Morocco along with a small population of uncertain 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. Because of uncertain paternity, males are integral to raising all 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 around 25 years old 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 North West Africa.
The Barbary macaque population of Gibraltar is the only such population outside Northern Africa and the only population of wild monkeys in Europe. The Rock of Gibraltar is populated by approximately 230 macaques.
The monkey is yellowish-brown to grey with a lighter underside. The Barbary macaque has a mean body length of 556.8 mm (21.9 in) in females and 634.3 mm (25.0 in) in males, and mean body weight is reported to be 9.9 ± 1.03 kg (21.8 lbs) in females and 14.5 ± 1.75 kg (32.0 lbs) 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. It is the only species of macaque that is distributed outside 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 in the Atlas Mountains, 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 behaviour 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. Because of this, infant calls do not have to differ dramatically for mothers to be able to recognize their own infant’s call. Mothers demonstrate different behaviours on hearing the calls of other infant macaques as opposed to the calls of their own offspring. 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 behaviour 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 behaviour 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 behaviour 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 behaviour in Barbary macaques. Density of macaques, however, is less correlated with the behaviour 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 an endangered species by the IUCN in 2009. Three-quarters of the world population is 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.[clarification needed]
The Barbary macaque is threatened by habitat loss, overgrazing and illegal capture. In Morocco, tourists interact with Barbary macaques in many regions. Information collected in the interviews with inhabitants in the High Atlas of Morocco indicated that the capture of macaques occurs in these regions. Conflict between local people and wild macaques is one of the greatest challenges to Macaca sylvanus conservation in Morocco. The main threats to the survival of Barbary macaques in this region have been found to be habitat destruction and the impact of livestock grazing, but there are also increasing problems of conflict with inhabitants due to crop raiding and the illegal capture of macaques. One study[which?] has found that the human–macaque conflict is mainly due to crop raiding. In the High Atlas of Morocco, macaques attract a large number of tourists every year, and they are favourable for their potential benefits to tourism. In addition, macaques have some ecological roles, for example they are the predators of several destructive insects and pests of plants and participate in seed dispersal in many plant species.
In the Central High Atlas, the Barbary macaque occurs in relatively small and fragmented areas restricted to the main valleys at altitudes of 700–2,400 m. In a 2013 study, researchers reported that they found Barbary macaques in relatively small and fragmented habitats in 10 sites, and that that the species no longer occurred in four localities. This could be attributed to habitat degradation, hunting activities, the impact of livestock grazing, and disturbance by people. As deforestation for agriculture and overgrazing continues, the remaining forest becomes increasingly fragmented. Consequently, the Barbary macaque is now restricted to small, fragmented relict habitats.
Human use and tourism
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.
Macaques in Morocco are frequently used as photo props, despite their protected status. Tourists are encouraged to take photos with the animals for a fee. Macaques are also sold as pets in Morocco and exported to Europe to be used as pets and fighting monkeys.
Tourists interact with wild monkeys across the globe and in some situations tourists may be encouraged to feed, photograph and touch the monkeys. Although tourism has the potential to bring money in towards conservation goals and provides an incentive for the protection of natural habitats, close proximity and interactions with tourists can also have significant psychological impacts on the Barbary macaque. Fecal samples and stress-indicating behaviours, such as belly scratching, indicate that the presence of tourists has a negative impact on the macaques. Human activities such as taking photographs cause the animals stress, possibly because the people come too close to the animals and make prolonged eye contact (a sign of aggression in many primates). Macaques that live in areas close to human contact have more parasites and lower overall health than those that live in wilder environments, at least in part due to the unhealthy diets they receive as a result of feeding from humans.
Several groups of Barbary macaque can be found in tourist sites, where they are affected by the presence of visitors providing food to them. Researchers comparing two such groups in the central High Atlas mountains in 2008 found that the tourist group of Barbary macaques spent significantly more time engaged in resting and aggressive behaviour, and foraged and moved significantly less than the wild group. The tourist group spent significantly less time per day feeding on herbs, seeds and acorns than the wild group. Human food accounted for 26% of the daily feeding records for the tourist group, and 1% for the wild-feeding group. Scientists who collected data on the seasonal activity budget and diet composition of the endangered Barbary macaque group inhabiting a tourist site in Morocco found that activity budgets and diet of the study group varied markedly among seasons and habitats. The percentage of daily time spent in foraging and moving was lowest in spring, and the daily time spent in resting was highest in spring and summer. The time budget devoted to aggressive display was highest in spring than the other three seasons. There is an increase in the daily feeding time spent eating flowers and fruits in summer, seeds, acorns, roots and barks in winter and autumn, herbs in spring and summer, and a clear increase in consumption of the human food in spring. The tourist and the wild groups did not differ in the proportion of daily records devoted to terrestrial feeding, but the tourist group spent a significantly lower percentage of daily records in terrestrial foraging, moving and resting, while performing more terrestrial aggressive displays more than the wild group. There was no significant difference between the two groups in the proportion of terrestrial feeding records spent eating fruits; but the tourist group had lower daily percentages of terrestrial feeding on leaves, seeds and acorns, roots and barks, and herbs, while it spent higher daily percentages of terrestrial feeding on human food.
There is evidence that Barbary macaques were traded or perhaps given as diplomatic gifts as long ago as the Iron Age. Their remains have been found in such sites as Emain Macha in Ireland, dating to no later than 95 BC; an Iron Age hillfort, the Titelberg in Luxembourg; and two Roman sites in Britain.
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 the town.
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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.