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Moor macaque

The Moor macaque (Macaca maura) is a macaque monkey with brown/black body fur with a pale rump patch and pink bare skin on the rump. It has ischial callosities, which are oval-shaped.[3] It is about 50–58.5 cm long, and eats figs, bamboo seeds, buds, sprouts, invertebrates and cereals in tropical rainforests. It is sometimes called "dog-ape" because of its dog-like muzzle, although it is no more closely related to apes than any other Old World monkey is. It is endemic to the island of Sulawesi in Indonesia, which is an important biodiversity hotspot.[3]

Moor macaque[1]
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Primates
Suborder: Haplorhini
Infraorder: Simiiformes
Family: Cercopithecidae
Genus: Macaca
Species:
M. maura
Binomial name
Macaca maura
(Schinz, 1825)
Moor macaque range

The Moor macaque is threatened mostly due to habitat loss from an expanding human population and deforestation to increase agricultural land area. The Macaca maura population is estimated to have decreased from 56,000 in 1983 to under 10,000 in 1994.[4] In 1992, Supriatna et al. 1992 conducted an extensive survey and found 6.3–63.2 individuals/km2.[2][5] They usually live in groups of 15-40 individuals,[6] with female philopatry and male dispersal and they are diurnal and semi-terrestrial. They spend a lot of their time in trees foraging and on the ground travelling.[7]

According to the Behavioural Data collection done on 2 groups of Moor macaques in the Bantimurung Bulusaraung National Park in South Sulawesi,[6] this species spends most of their time feeding in places where food resources are abundant. The results also show that Moor macaques tend to spend more time foraging as the group size increases as they spend less time in alertness.

The population of this species is highly endangered due to serious anthropogenic activities like agriculture and tourism, which contribute to its habitat loss.[8] Like many other frugivorous primates, Moor macaques  have made significant contributions to the environment, helping to support high densities of seedlings and saplings as well as the process of gene flow among plant populations. This is crucial for sustaining forest regeneration and restoring vegetation in degraded forests.[9]

This species has been on the IUCN Red list of threatened species (A2cd) since 2015.[10]

Taxonomy edit

The Moor macaque made its first appearance in western science through the work of Heinrich Rudolf Schinz in 1825.[11]

Distribution and habitat edit

The Indonesian island of Sulawesi hosts 7 species of macaques with one of them being the Moor macaque. Unfortunately, the Moor macaque is endemic to the island and is considered to be endangered by the IUCN Red List of Threatened Species. The Moor macaque is the only species of macaques that existed naturally in South Sulawesi. Moor macaques have significant ecological flexibility that enables them to use several forest strata, including secondary habitats.[12] They have a different ecological environment compared to other nonhuman primates since they have no major predators or competitors except where their ranges overlap.[12] The home range of the Moor macaque group is usually 20-30 ha wide, with a total distance of roughly 6.64 km.[9]

They can be found in lowland forests, grasslands, limestone areas and even near human habitations,[9] and they are commonly found with the endemic Malkoha birds that feed on grasshoppers, which are pushed out of the canopy by the macaques' movements.[12]

Those living near humans have been observed to be more present in areas where domestic animals are found, as these areas do not have a lot of traps that endanger them.[8] They are predominantly found in the karst forest ecosystem of South Sulawesi. The karst plain forest is more resourceful for these macaques as the latter contains an abundance of food. Researchers discovered that out of the 107 identified tree species, 74 of them were vital macaque food species with the remaining being food species of secondary importance.[8] The latter information was put together due to a study that took place in the Bantimurung Bulusaraung National Park and specifically in the Karaenta area, a former nature reserve, where high density of fig trees as well as the fact that the Karaenta forest is separated from bigger forest tracts have led to a high population density of Moor macaques. As a result, Moor macaques have limited home ranges at this location.[12]

The karst tower forest is less useful for the macaques in terms of acquiring food or other related resources but acts as a natural refuge from human disturbance. Another important area with significant Moor macaques is the Tabo-tabo forest in Pangkep and is considered to be a secondary forest area. The home range for primates is characterised by three factors; food availability, the distribution of the food, and the interval of changing fruit seasons.The Tabo-tabo forest is characterised as a secondary lowland forest and the latter created a suitable environment for the growth of plants on fertile alluvial and Mediterranean red soils.The high diversity of plants and shelter provision in the area made the land extremely suitable for these macaques to thrive.[9]

Behavior edit

The most common behavioural activities of Moor macaques are feeding, followed by moving, resting, and social interaction. [9]

Moor macaques are a male dispersing species. Males leave the groups in which they are born between the ages of 7 and 9, while females stay in their birth groups. This has an important purpose, it avoids inbreeding and broadens the genetic pool of the groups.[3] Moor macaques groups have been observed to be tolerant and not very aggressive.[13] Group fission occurs in Moor macaques, competition between females for food does not seem to be the reason for fission.[14] However, some studies relate group fission to competition among females for food resources, others attribute it to increased sexual competition among males, and some others relate this phenomenon to establishing home ranges, specifically in Moor macaque groups with overlapped home ranges.[14]

The Sulawesi macaques, including Moor macaques, are further distinguishable from other macaques by their quiet bared-teeth display and the uttering of a loud call. Rather than conveying submission, as in most macaque species, the quiet bared-teeth display is thought to express the emitter's peaceful intentions, promoting positive interactions. All Sulawesi macaques, particularly adult males have emit a loud call, a particular, bird-like vocalization.[12]

During agonistic encounters, wild Moor macaques have low inter-individual distances, uncommon strong aggression, a strong conciliatory tendency, and limited support for kin.[12]

Predation is a key evolutionary factor. Snakes are one of the most prevalent primate predators, and the primates’ quick detection of predators may have contributed to the evolution of their visual and perceptual skills. When primates notice a snake, they frequently respond by making alarm calls that attract and/or notify other members of the group about its presence, and/or by mobbing it.[15]

Sexual behavior edit

Perineal swelling is an important factor in the sexual life of Moor macaques. As this species does not have a marked reproductive season, not all females swell at the same time.[14] Females start to swell between the age of 4 years and 6 years and have their first child between the age of 6 years and 7 years. Swelling individuals are more likely mounted by the males than non-swelling ones. The dominant and oldest female of the group is usually mounted by the alpha male. Non-alpha males only mount females when the alpha is out of sight and lower ranking males usually mount non-swelling females, although in most Moor macaque groups, there is only one male.[16] Poor dietary factors appear to be associated with a delay in the onset of perineal swelling and first parturition. [17]

From the end of the rainy season to the start of the dry season, there appeared to be a rise in births. The moor macaques are classified as moderately seasonal breeders based on the fact that 33-67% of their newborns occur in a single three-month period. The peak might be explained by yearly increases in food supply, particularly a rise in fruit.[17]

Female reproductive state differences within a group may have an effect on female furcation patterns, which may be more noticeable in egalitarian species where social interactions are less impacted by dominance or kinship. This furcation pattern may be caused by the tendency of adult females that are not cycling to stay near to one another.[14]

Social behavior edit

 
Grooming among Moor macaques[18]

Changes in group fission process and furcation patterns may reflect differences in social characteristics among species as well as ecological and demographic differences among populations; thus, studies of group fission may contribute to our general understanding of why primates live in a variety of groupings.[19]

Special relationships between certain males and females can either trigger or encourage group fission. In Moor macaques, however, significant connection between specific males and females does not appear to affect the process of fission.[19] Moor macaque females are not actively involved in intergroup interactions. On the other hand, male aggression toward other groups is significantly more frequent than female aggression.[12] Adult female furcation patterns can be anticipated by their connection with one another, such as grooming behavior, prior to group fission. However, the grooming habit of mature female Moor macaques was unrelated to the furcation.[19] Individuals of similar age, sex, or rank tend to stay close to one another.[19]

Moor macaques are an ideal taxon to examine interspecific diversity in play behavior among nonhuman primates.[20] Play is an excessive, spontaneous, and self-rewarding behavior that serves no immediate purpose and frequently takes place in non-stressful circumstances.[20] Moor macaques spend a larger proportion of their time in solitary and social play than in grooming interactions. Play sessions in Moor macaques include more individuals, large variety of play behaviors, great play face rates, great proportion of time in contact play, and high rate of reciprocal play‐biting. Aggressive escalations were not common in Moor macaques.[20]

 
Feeding behavior observed in Moor macaques[21]

Diet edit

Despite their frequently changing habitats, Moor macaques are characterized by having a flexible diet.[12] Insects and other food items, including shoots and young leaves, are essential resources for Moor macaques, particularly in extensively altered habitats.[12] The tree species known to be a diet are Garcinia nervosa, Arenga pinnata, Flacourtia rukam, Ficus. sp, Eugenia cuminii, Gastonia serratifolia, Mangifera sp., Spondias dulcis, and Muntingia calabura.[9]

Compared to other macaques, kinship in Moor macaques may have less of an influence on proximity during feeding. Weak kinship effects during feeding may be caused by a lack of food competition within the group.[19] When within-group competition (WGC) for food resources is intense, lower-ranking females are likely to move away from original groupings and create new smaller groups.[14]

Maternity edit

Moor macaques usually stay close to their matrilineal relatives more when they are moving or resting than when they are feeding.

Females are in close proximity to females with newborn infants, regardless of the group's stage of activity.[19]

Interaction with humans edit

Anthropogenic factors such as habitat fragmentation, alterations, along with non-species-specific hunting traps in the forest have become major risks to the Moor macaques' survival, with more than half of the population declining over three decades.[8][9]

Due to anthropogenic activities, Moor Macaque interactions with humans have increased. Primates are often victims of such occurrences because they have a hard time adapting to environmental disturbances.[22] Due to their endemic status to the island of Sulawesi, most of their interactions used to be with the Bantimurung Bulusaraung National Park staff and researchers who would feed them, which is considered as consistent provisioning. Starting the year 2015, they started interacting with vehicles that would drive along a road located in their home range, which is considered as inconsistent provisioning.[22] Based on the available research, human interaction damages the social networks of these macaques, and the latter is necessary for increase of infant survival, social ranking, reproductive success, and even enhanced thermoregulation during winter.[22]

According to a study about the habituation process, Moor macaques react differently to the presence of humans depending on their previous interactions with them. Moor macaques are better approached in areas of greater visibility with more trees.[23] Food provisioning, in which people purposefully offer food to nonhuman primates, may result in rapid habituation of wildlife such that they approach humans for food, take food from their hands, and perhaps aggress toward them to elicit provisioning behavior.[22] Provisioning can lead to reduced foraging energy consumption in monkeys, more time for resting and social behavior, and higher birth rates, provisioned foods can be good energy sources. However, because it is linked to a higher risk of injury, zoonotic disease transmission, and direct human interaction, provisioning may also be potentially dangerous for monkeys and other wildlife species.[22]

Studies have found that the relatively widespread habit of pet macaque ownership among a variety of ethnic and religious groups on the island explain the bidirectional disease transmission. The majority of Sulawesi macaques kept as pets are captured as infants by opportunistically trapping wild mother-infant pairs or by using traps to reduce crop raiding, which resulted in competition for resources.[12] Moor macaques’ encounter rate is lower in areas with more open spaces and with no trees than in areas with greater forest cover. Moreover, the individual encounter rate is lower when more traps are found in an area and higher when more domestic animals are sighted in the area.[8]

Conservation edit

The tourism industry, hunting, agriculture and logging are some of the big threats to the Moor macaques because they highly contribute to their habitat loss.[8] This resulted in the change and loss of 80% of Sulawesi's forests, with just 30% remaining in good condition - which means forest canopy unbroken by large clearings and only scattered signs of human activity. Therefore, Moor macaques’ conservation has become a broader concern.[12]

Even in areas that are under local protection, deforestation is still observed in many forests of the southern parts of the Sulawesi Island,[8] thus conservation of the population of Moor macaques should be a priority since its population is declining at a high rate. For conservation purposes, information on life histories and demography is essential. The conservation status of Moor macaques is considered high. However, due to significant habitat degradation, the condition of Moor macaques does not warrant optimism. It has been recommended that new reserves be established as well as expanding the existing reserves.[17] Based on a study, challenges for species and their conservation efforts occurred as a result of the shrinking of forest areas and the deterioration of forest quality as habitat. Additionally, growing human populations have had a substantial negative influence on both populations and habitats of Moor macaques.[9]

According to a study done on the effects of anthropogenic activities on the population of Moor macaques, the population density of Moor macaques is low outside of protected areas and support the study's hypothesis that the population of this species is declining in several regions, especially in the southern forests of the species’ geographic range. Furthermore, they found a high presence of anthropogenic activity in forests inhabited by Moor macaques, and a negative effect of the number of non species-specific hunting traps in the forest on macaque encounter rate.[8] In the National Park of Chamba District, South Sulawesi, there was an observed decrease in Moor macaques due to human settlement and road traffics which endanger the life of Moor macaques through food poisoning, and road accidents.

During a survey in South Sulawesi, there was a high encounter of Moor macaques in agroforests, where it was seen that Moor macaques like feeding on corn. This is a sign that different types of plantations can influence the distribution and encounter rate of Moor macaques.[8] This, with different interviews with local people inhabiting the area surveyed, combining a well conserved forest with small agricultural patches on landscape scape can have a positive effect on the conservation of Moor macaques. With other studies done on the effect of agroforests on the conservation of Moor macaques,[24][25][26] it has been observed that agroforests and forests cover can positively affect or increase the population of Moor macaques. Therefore, for better conservation and for the benefit of remnant subpopulations, forests in South Sulawesi Island should be protected and conserved. Raising awareness of the ecological importance of Moor macaques, and motivating people to conduct activities that are ecologically sustainable are also good actions towards the conservation of Moor macaques. While there are some studies done in South Sulawesi, more studies have to be conducted on other parts of the Island for an adequate conservation of this species.[8]

References edit

  1. ^ Groves, C. P. (2005). Wilson, D. E.; Reeder, D. M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Baltimore: Johns Hopkins University Press. pp. 162–163. ISBN 0-801-88221-4. OCLC 62265494.
  2. ^ a b Supriatna, J.; Shekelle, M. & Burton, J. (2008). "Macaca maura". The IUCN Red List of Threatened Species. 2008. IUCN: e.T12553A3356200. doi:10.2305/IUCN.UK.2008.RLTS.T12553A3356200.en.
  3. ^ a b c Evans, B. J.; Supriatna, J.; Melnick, D. J. (2001). "Hybridization and Population Genetics of Two Macaque Species in Sulawesi, Indonesia". Evolution. 55 (8): 1686–2302. doi:10.1554/0014-3820(2001)055[1686:hapgot]2.0.co;2. ISSN 0014-3820. PMID 11580028.
  4. ^ Evans, B. J.; Supriatna, J.; Melnick, D. J. (2001). "Hybridization and population genetics of two macaque species in Sulawesi, Indonesia". Evolution. 55 (8). The Society for the Study of Evolution: 1688. doi:10.1111/j.0014-3820.2001.tb00688.x. PMID 11580028.
  5. ^ Supriatna, Jatna; Froehlich, Jeffrey W.; Erwin, Joseph M.; Southwick, Charles H. (1992). "Population, habitat and conservation status of Macaca maurus, Macaca tonkeana and their putative hybrids". Tropical Biodiversity. 1 (1): 31–48.
  6. ^ a b Albani, Alessandro; Cutini, Maurizio; Germani, Lavinia; Riley, Erin P.; Ngakan, Putu Oka; Carosi, Monica (September 2020). "Activity budget, home range, and habitat use of moor macaques (Macaca maura) in the karst forest of South Sulawesi, Indonesia". Primates. 61 (5): 673–684. doi:10.1007/s10329-020-00811-8. ISSN 0032-8332. PMID 32170514. S2CID 212681229.
  7. ^ "Moor Macaque | New England Primate Conservancy". 2021-12-11. Retrieved 2022-04-12.
  8. ^ a b c d e f g h i j Beltrán Francés, Víctor; Spaan, Denise; Amici, Federica; Maulany, Risma Illa; Putu Oka, Ngakan; Majolo, Bonaventura (April 2022). "Effect of Anthropogenic Activities on the Population of Moor Macaques (Macaca maura) in South Sulawesi, Indonesia". International Journal of Primatology. 43 (2): 339–359. doi:10.1007/s10764-022-00279-x. ISSN 0164-0291. S2CID 247068580.
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  11. ^ "Species+". speciesplus.net. Retrieved 2022-04-12.
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  13. ^ Riley, Erin P.; Sagnotti, Cristina; Carosi, Monica; Putu Oka, Ngakan (2014-01-01). "Socially tolerant relationships among wild male moor macaques (Macaca maura)". Behaviour. 151 (7): 1021–1044. doi:10.1163/1568539X-00003182. ISSN 0005-7959.
  14. ^ a b c d e Okamoto, Kyoko; Matsumura, Shuichi (2001-06-01). "Group Fission in Moor Macaques (Macaca maurus)". International Journal of Primatology. 22 (3): 481–493. doi:10.1023/A:1010711813637. ISSN 1573-8604. S2CID 20928082.
  15. ^ Hernández Tienda, Clara; Beltrán Francés, Víctor; Majolo, Bonaventura; Romero, Teresa; Illa Maulany, Risma; Oka Ngakan, Putu; Amici, Federica (2021-08-01). "Reaction to Snakes in Wild Moor Macaques (Macaca maura)". International Journal of Primatology. 42 (4): 528–532. doi:10.1007/s10764-021-00230-6. ISSN 1573-8604. S2CID 237853435.
  16. ^ Matsumura, Shuichi (January 1993). "Female reproductive cycles and the sexual behavior of moor macaques (Macaca maurus) in their natural habitat, South Sulawesi, Indonesia". Primates. 34 (1): 99–103. doi:10.1007/BF02381286. ISSN 0032-8332. S2CID 33436234.
  17. ^ a b c Okamoto, K.; Matsumura, S.; Watanabe, K. (2000). "Life history and demography of wild moor macaques (Macaca maurus): summary of ten years of observations". American Journal of Primatology. 52 (1): 1–11. doi:10.1002/1098-2345(200009)52:1<1::AID-AJP1>3.0.CO;2-F. ISSN 0275-2565. PMID 10993134. S2CID 24476587.
  18. ^ "File:Toilettage macaca maura.jpg - Wikimedia Commons". commons.wikimedia.org. Retrieved 2022-12-01.
  19. ^ a b c d e f Matsumura, Shuichi; Okamoto, Kyoko (1997-12-01). "Factors Affecting Proximity Among Members of a Wild Group of Moor Macaques During Feeding, Moving, and Resting". International Journal of Primatology. 18 (6): 929–940. doi:10.1023/A:1026344129760. ISSN 1573-8604. S2CID 45107000.
  20. ^ a b c Beltrán Francés, Víctor; Castellano-Navarro, Alba; Illa Maulany, Risma; Ngakan, Putu O.; MacIntosh, Andrew J. J.; Llorente, Miquel; Amici, Federica (2020-09-03). "Play behavior in immature moor macaques (Macaca maura) and Japanese macaques (Macaca fuscata)". American Journal of Primatology. 82 (10): e23192. doi:10.1002/ajp.23192. ISSN 1098-2345. PMID 32882065. S2CID 221496191.
  21. ^ "File:Macaca maura groupe.jpg - Wikimedia Commons". commons.wikimedia.org. Retrieved 2022-12-01.
  22. ^ a b c d e Morrow, Kristen S.; Glanz, Hunter; Ngakan, Putu Oka; Riley, Erin P. (December 2019). "Interactions with humans are jointly influenced by life history stage and social network factors and reduce group cohesion in moor macaques (Macaca maura)". Scientific Reports. 9 (1): 20162. Bibcode:2019NatSR...920162M. doi:10.1038/s41598-019-56288-z. ISSN 2045-2322. PMC 6934674. PMID 31882849.
  23. ^ Hernández Tienda, Clara; Majolo, Bonaventura; Romero, Teresa; Illa Maulany, Risma; Oka Ngakan, Putu; Beltrán Francés, Víctor; Gregorio Hernández, Elisa; Gómez-Melara, Jose; Llorente, Miquel; Amici, Federica (2022-04-01). "The Habituation Process in Two Groups of Wild Moor Macaques (Macaca maura)". International Journal of Primatology. 43 (2): 291–316. doi:10.1007/s10764-021-00275-7. ISSN 1573-8604. PMC 8758468. PMID 35043025.
  24. ^ Campbell-Smith, Gail; Simanjorang, Hubert V.P.; Leader-Williams, Nigel; Linkie, Matthew (2010). "Local attitudes and perceptions toward crop-raiding by orangutans (Pongo abelii) and other nonhuman primates in northern Sumatra, Indonesia". American Journal of Primatology. 72 (10): 866–876. doi:10.1002/ajp.20822. PMID 20301138. S2CID 5757864.
  25. ^ Estrada, Alejandro; Raboy, Becky E.; Oliveira, Leonardo C. (2012). "Agroecosystems and Primate Conservation in the Tropics: A Review". American Journal of Primatology. 74 (8): 696–711. doi:10.1002/ajp.22033. PMID 22605526. S2CID 205329975.
  26. ^ Riley, Erin P.; Priston, Nancy E. C. (2010). "Macaques in farms and folklore: Exploring the human-nonhuman primate interface in Sulawesi, Indonesia". American Journal of Primatology. 72 (10): 848–854. doi:10.1002/ajp.20798. PMID 20146249. S2CID 23446462.

External links edit

  • Photos at ARKive.

moor, macaque, macaca, maura, macaque, monkey, with, brown, black, body, with, pale, rump, patch, pink, bare, skin, rump, ischial, callosities, which, oval, shaped, about, long, eats, figs, bamboo, seeds, buds, sprouts, invertebrates, cereals, tropical, rainfo. The Moor macaque Macaca maura is a macaque monkey with brown black body fur with a pale rump patch and pink bare skin on the rump It has ischial callosities which are oval shaped 3 It is about 50 58 5 cm long and eats figs bamboo seeds buds sprouts invertebrates and cereals in tropical rainforests It is sometimes called dog ape because of its dog like muzzle although it is no more closely related to apes than any other Old World monkey is It is endemic to the island of Sulawesi in Indonesia which is an important biodiversity hotspot 3 Moor macaque 1 Conservation status Endangered IUCN 3 1 2 Scientific classification Domain Eukaryota Kingdom Animalia Phylum Chordata Class Mammalia Order Primates Suborder Haplorhini Infraorder Simiiformes Family Cercopithecidae Genus Macaca Species M maura Binomial name Macaca maura Schinz 1825 Moor macaque range The Moor macaque is threatened mostly due to habitat loss from an expanding human population and deforestation to increase agricultural land area The Macaca maura population is estimated to have decreased from 56 000 in 1983 to under 10 000 in 1994 4 In 1992 Supriatna et al 1992 conducted an extensive survey and found 6 3 63 2 individuals km2 2 5 They usually live in groups of 15 40 individuals 6 with female philopatry and male dispersal and they are diurnal and semi terrestrial They spend a lot of their time in trees foraging and on the ground travelling 7 According to the Behavioural Data collection done on 2 groups of Moor macaques in the Bantimurung Bulusaraung National Park in South Sulawesi 6 this species spends most of their time feeding in places where food resources are abundant The results also show that Moor macaques tend to spend more time foraging as the group size increases as they spend less time in alertness The population of this species is highly endangered due to serious anthropogenic activities like agriculture and tourism which contribute to its habitat loss 8 Like many other frugivorous primates Moor macaques have made significant contributions to the environment helping to support high densities of seedlings and saplings as well as the process of gene flow among plant populations This is crucial for sustaining forest regeneration and restoring vegetation in degraded forests 9 This species has been on the IUCN Red list of threatened species A2cd since 2015 10 Contents 1 Taxonomy 2 Distribution and habitat 3 Behavior 3 1 Sexual behavior 3 2 Social behavior 3 3 Diet 3 4 Maternity 4 Interaction with humans 5 Conservation 6 References 7 External linksTaxonomy editThe Moor macaque made its first appearance in western science through the work of Heinrich Rudolf Schinz in 1825 11 Distribution and habitat editThe Indonesian island of Sulawesi hosts 7 species of macaques with one of them being the Moor macaque Unfortunately the Moor macaque is endemic to the island and is considered to be endangered by the IUCN Red List of Threatened Species The Moor macaque is the only species of macaques that existed naturally in South Sulawesi Moor macaques have significant ecological flexibility that enables them to use several forest strata including secondary habitats 12 They have a different ecological environment compared to other nonhuman primates since they have no major predators or competitors except where their ranges overlap 12 The home range of the Moor macaque group is usually 20 30 ha wide with a total distance of roughly 6 64 km 9 They can be found in lowland forests grasslands limestone areas and even near human habitations 9 and they are commonly found with the endemic Malkoha birds that feed on grasshoppers which are pushed out of the canopy by the macaques movements 12 Those living near humans have been observed to be more present in areas where domestic animals are found as these areas do not have a lot of traps that endanger them 8 They are predominantly found in the karst forest ecosystem of South Sulawesi The karst plain forest is more resourceful for these macaques as the latter contains an abundance of food Researchers discovered that out of the 107 identified tree species 74 of them were vital macaque food species with the remaining being food species of secondary importance 8 The latter information was put together due to a study that took place in the Bantimurung Bulusaraung National Park and specifically in the Karaenta area a former nature reserve where high density of fig trees as well as the fact that the Karaenta forest is separated from bigger forest tracts have led to a high population density of Moor macaques As a result Moor macaques have limited home ranges at this location 12 The karst tower forest is less useful for the macaques in terms of acquiring food or other related resources but acts as a natural refuge from human disturbance Another important area with significant Moor macaques is the Tabo tabo forest in Pangkep and is considered to be a secondary forest area The home range for primates is characterised by three factors food availability the distribution of the food and the interval of changing fruit seasons The Tabo tabo forest is characterised as a secondary lowland forest and the latter created a suitable environment for the growth of plants on fertile alluvial and Mediterranean red soils The high diversity of plants and shelter provision in the area made the land extremely suitable for these macaques to thrive 9 Behavior editThe most common behavioural activities of Moor macaques are feeding followed by moving resting and social interaction 9 Moor macaques are a male dispersing species Males leave the groups in which they are born between the ages of 7 and 9 while females stay in their birth groups This has an important purpose it avoids inbreeding and broadens the genetic pool of the groups 3 Moor macaques groups have been observed to be tolerant and not very aggressive 13 Group fission occurs in Moor macaques competition between females for food does not seem to be the reason for fission 14 However some studies relate group fission to competition among females for food resources others attribute it to increased sexual competition among males and some others relate this phenomenon to establishing home ranges specifically in Moor macaque groups with overlapped home ranges 14 The Sulawesi macaques including Moor macaques are further distinguishable from other macaques by their quiet bared teeth display and the uttering of a loud call Rather than conveying submission as in most macaque species the quiet bared teeth display is thought to express the emitter s peaceful intentions promoting positive interactions All Sulawesi macaques particularly adult males have emit a loud call a particular bird like vocalization 12 During agonistic encounters wild Moor macaques have low inter individual distances uncommon strong aggression a strong conciliatory tendency and limited support for kin 12 Predation is a key evolutionary factor Snakes are one of the most prevalent primate predators and the primates quick detection of predators may have contributed to the evolution of their visual and perceptual skills When primates notice a snake they frequently respond by making alarm calls that attract and or notify other members of the group about its presence and or by mobbing it 15 Sexual behavior edit Perineal swelling is an important factor in the sexual life of Moor macaques As this species does not have a marked reproductive season not all females swell at the same time 14 Females start to swell between the age of 4 years and 6 years and have their first child between the age of 6 years and 7 years Swelling individuals are more likely mounted by the males than non swelling ones The dominant and oldest female of the group is usually mounted by the alpha male Non alpha males only mount females when the alpha is out of sight and lower ranking males usually mount non swelling females although in most Moor macaque groups there is only one male 16 Poor dietary factors appear to be associated with a delay in the onset of perineal swelling and first parturition 17 From the end of the rainy season to the start of the dry season there appeared to be a rise in births The moor macaques are classified as moderately seasonal breeders based on the fact that 33 67 of their newborns occur in a single three month period The peak might be explained by yearly increases in food supply particularly a rise in fruit 17 Female reproductive state differences within a group may have an effect on female furcation patterns which may be more noticeable in egalitarian species where social interactions are less impacted by dominance or kinship This furcation pattern may be caused by the tendency of adult females that are not cycling to stay near to one another 14 Social behavior edit nbsp Grooming among Moor macaques 18 Changes in group fission process and furcation patterns may reflect differences in social characteristics among species as well as ecological and demographic differences among populations thus studies of group fission may contribute to our general understanding of why primates live in a variety of groupings 19 Special relationships between certain males and females can either trigger or encourage group fission In Moor macaques however significant connection between specific males and females does not appear to affect the process of fission 19 Moor macaque females are not actively involved in intergroup interactions On the other hand male aggression toward other groups is significantly more frequent than female aggression 12 Adult female furcation patterns can be anticipated by their connection with one another such as grooming behavior prior to group fission However the grooming habit of mature female Moor macaques was unrelated to the furcation 19 Individuals of similar age sex or rank tend to stay close to one another 19 Moor macaques are an ideal taxon to examine interspecific diversity in play behavior among nonhuman primates 20 Play is an excessive spontaneous and self rewarding behavior that serves no immediate purpose and frequently takes place in non stressful circumstances 20 Moor macaques spend a larger proportion of their time in solitary and social play than in grooming interactions Play sessions in Moor macaques include more individuals large variety of play behaviors great play face rates great proportion of time in contact play and high rate of reciprocal play biting Aggressive escalations were not common in Moor macaques 20 nbsp Feeding behavior observed in Moor macaques 21 Diet edit Despite their frequently changing habitats Moor macaques are characterized by having a flexible diet 12 Insects and other food items including shoots and young leaves are essential resources for Moor macaques particularly in extensively altered habitats 12 The tree species known to be a diet are Garcinia nervosa Arenga pinnata Flacourtia rukam Ficus sp Eugenia cuminii Gastonia serratifolia Mangifera sp Spondias dulcis and Muntingia calabura 9 Compared to other macaques kinship in Moor macaques may have less of an influence on proximity during feeding Weak kinship effects during feeding may be caused by a lack of food competition within the group 19 When within group competition WGC for food resources is intense lower ranking females are likely to move away from original groupings and create new smaller groups 14 Maternity edit Moor macaques usually stay close to their matrilineal relatives more when they are moving or resting than when they are feeding Females are in close proximity to females with newborn infants regardless of the group s stage of activity 19 Interaction with humans editAnthropogenic factors such as habitat fragmentation alterations along with non species specific hunting traps in the forest have become major risks to the Moor macaques survival with more than half of the population declining over three decades 8 9 Due to anthropogenic activities Moor Macaque interactions with humans have increased Primates are often victims of such occurrences because they have a hard time adapting to environmental disturbances 22 Due to their endemic status to the island of Sulawesi most of their interactions used to be with the Bantimurung Bulusaraung National Park staff and researchers who would feed them which is considered as consistent provisioning Starting the year 2015 they started interacting with vehicles that would drive along a road located in their home range which is considered as inconsistent provisioning 22 Based on the available research human interaction damages the social networks of these macaques and the latter is necessary for increase of infant survival social ranking reproductive success and even enhanced thermoregulation during winter 22 According to a study about the habituation process Moor macaques react differently to the presence of humans depending on their previous interactions with them Moor macaques are better approached in areas of greater visibility with more trees 23 Food provisioning in which people purposefully offer food to nonhuman primates may result in rapid habituation of wildlife such that they approach humans for food take food from their hands and perhaps aggress toward them to elicit provisioning behavior 22 Provisioning can lead to reduced foraging energy consumption in monkeys more time for resting and social behavior and higher birth rates provisioned foods can be good energy sources However because it is linked to a higher risk of injury zoonotic disease transmission and direct human interaction provisioning may also be potentially dangerous for monkeys and other wildlife species 22 Studies have found that the relatively widespread habit of pet macaque ownership among a variety of ethnic and religious groups on the island explain the bidirectional disease transmission The majority of Sulawesi macaques kept as pets are captured as infants by opportunistically trapping wild mother infant pairs or by using traps to reduce crop raiding which resulted in competition for resources 12 Moor macaques encounter rate is lower in areas with more open spaces and with no trees than in areas with greater forest cover Moreover the individual encounter rate is lower when more traps are found in an area and higher when more domestic animals are sighted in the area 8 Conservation editThe tourism industry hunting agriculture and logging are some of the big threats to the Moor macaques because they highly contribute to their habitat loss 8 This resulted in the change and loss of 80 of Sulawesi s forests with just 30 remaining in good condition which means forest canopy unbroken by large clearings and only scattered signs of human activity Therefore Moor macaques conservation has become a broader concern 12 Even in areas that are under local protection deforestation is still observed in many forests of the southern parts of the Sulawesi Island 8 thus conservation of the population of Moor macaques should be a priority since its population is declining at a high rate For conservation purposes information on life histories and demography is essential The conservation status of Moor macaques is considered high However due to significant habitat degradation the condition of Moor macaques does not warrant optimism It has been recommended that new reserves be established as well as expanding the existing reserves 17 Based on a study challenges for species and their conservation efforts occurred as a result of the shrinking of forest areas and the deterioration of forest quality as habitat Additionally growing human populations have had a substantial negative influence on both populations and habitats of Moor macaques 9 According to a study done on the effects of anthropogenic activities on the population of Moor macaques the population density of Moor macaques is low outside of protected areas and support the study s hypothesis that the population of this species is declining in several regions especially in the southern forests of the species geographic range Furthermore they found a high presence of anthropogenic activity in forests inhabited by Moor macaques and a negative effect of the number of non species specific hunting traps in the forest on macaque encounter rate 8 In the National Park of Chamba District South Sulawesi there was an observed decrease in Moor macaques due to human settlement and road traffics which endanger the life of Moor macaques through food poisoning and road accidents During a survey in South Sulawesi there was a high encounter of Moor macaques in agroforests where it was seen that Moor macaques like feeding on corn This is a sign that different types of plantations can influence the distribution and encounter rate of Moor macaques 8 This with different interviews with local people inhabiting the area surveyed combining a well conserved forest with small agricultural patches on landscape scape can have a positive effect on the conservation of Moor macaques With other studies done on the effect of agroforests on the conservation of Moor macaques 24 25 26 it has been observed that agroforests and forests cover can positively affect or increase the population of Moor macaques Therefore for better conservation and for the benefit of remnant subpopulations forests in South Sulawesi Island should be protected and conserved Raising awareness of the ecological importance of Moor macaques and motivating people to conduct activities that are ecologically sustainable are also good actions towards the conservation of Moor macaques While there are some studies done in South Sulawesi more studies have to be conducted on other parts of the Island for an adequate conservation of this species 8 References edit Groves C P 2005 Wilson D E Reeder D M eds Mammal Species of the World A Taxonomic and Geographic Reference 3rd ed Baltimore Johns Hopkins University Press pp 162 163 ISBN 0 801 88221 4 OCLC 62265494 a b Supriatna J Shekelle M amp Burton J 2008 Macaca maura The IUCN Red List of Threatened Species 2008 IUCN e T12553A3356200 doi 10 2305 IUCN UK 2008 RLTS T12553A3356200 en a b c Evans B J Supriatna J Melnick D J 2001 Hybridization and Population Genetics of Two Macaque Species in Sulawesi Indonesia Evolution 55 8 1686 2302 doi 10 1554 0014 3820 2001 055 1686 hapgot 2 0 co 2 ISSN 0014 3820 PMID 11580028 Evans B J Supriatna J Melnick D J 2001 Hybridization and population genetics of two macaque species in Sulawesi Indonesia Evolution 55 8 The Society for the Study of Evolution 1688 doi 10 1111 j 0014 3820 2001 tb00688 x PMID 11580028 Supriatna Jatna Froehlich Jeffrey W Erwin Joseph M Southwick Charles H 1992 Population habitat and conservation status of Macaca maurus Macaca tonkeana and their putative hybrids Tropical Biodiversity 1 1 31 48 a b Albani Alessandro Cutini Maurizio Germani Lavinia Riley Erin P Ngakan Putu Oka Carosi Monica September 2020 Activity budget home range and habitat use of moor macaques Macaca maura in the karst forest of South Sulawesi Indonesia Primates 61 5 673 684 doi 10 1007 s10329 020 00811 8 ISSN 0032 8332 PMID 32170514 S2CID 212681229 Moor Macaque New England Primate Conservancy 2021 12 11 Retrieved 2022 04 12 a b c d e f g h i j Beltran Frances Victor Spaan Denise Amici Federica Maulany Risma Illa Putu Oka Ngakan Majolo Bonaventura April 2022 Effect of Anthropogenic Activities on the Population of Moor Macaques Macaca maura in South Sulawesi Indonesia International Journal of Primatology 43 2 339 359 doi 10 1007 s10764 022 00279 x ISSN 0164 0291 S2CID 247068580 a b c d e f g h Maulany R I Putra G T S Nasri N Hamzah A S Ngakan P O 2021 11 01 Initial Investigation of Sulawesi Moor Macaque Macaca maura in Tabo tabo Forest South Sulawesi Indonesia IOP Conference Series Earth and Environmental Science 886 1 012033 Bibcode 2021E amp ES 886a2033M doi 10 1088 1755 1315 886 1 012033 ISSN 1755 1307 S2CID 244305364 Macaca maura Riley E Lee R Sangermano F Cannon C amp Shekelle M 2015 11 22 doi 10 2305 iucn uk 2020 3 rlts t12553a197831931 en S2CID 239444667 a href Template Cite journal html title Template Cite journal cite journal a Cite journal requires journal help Species speciesplus net Retrieved 2022 04 12 a b c d e f g h i j k Riley Erin P February 18 2010 The endemic seven Four decades of research on the Sulawesi macaques Evolutionary Anthropology Issues News and Reviews 19 1 22 36 doi 10 1002 evan 20246 S2CID 83850280 Riley Erin P Sagnotti Cristina Carosi Monica Putu Oka Ngakan 2014 01 01 Socially tolerant relationships among wild male moor macaques Macaca maura Behaviour 151 7 1021 1044 doi 10 1163 1568539X 00003182 ISSN 0005 7959 a b c d e Okamoto Kyoko Matsumura Shuichi 2001 06 01 Group Fission in Moor Macaques Macaca maurus International Journal of Primatology 22 3 481 493 doi 10 1023 A 1010711813637 ISSN 1573 8604 S2CID 20928082 Hernandez Tienda Clara Beltran Frances Victor Majolo Bonaventura Romero Teresa Illa Maulany Risma Oka Ngakan Putu Amici Federica 2021 08 01 Reaction to Snakes in Wild Moor Macaques Macaca maura International Journal of Primatology 42 4 528 532 doi 10 1007 s10764 021 00230 6 ISSN 1573 8604 S2CID 237853435 Matsumura Shuichi January 1993 Female reproductive cycles and the sexual behavior of moor macaques Macaca maurus in their natural habitat South Sulawesi Indonesia Primates 34 1 99 103 doi 10 1007 BF02381286 ISSN 0032 8332 S2CID 33436234 a b c Okamoto K Matsumura S Watanabe K 2000 Life history and demography of wild moor macaques Macaca maurus summary of ten years of observations American Journal of Primatology 52 1 1 11 doi 10 1002 1098 2345 200009 52 1 lt 1 AID AJP1 gt 3 0 CO 2 F ISSN 0275 2565 PMID 10993134 S2CID 24476587 File Toilettage macaca maura jpg Wikimedia Commons commons wikimedia org Retrieved 2022 12 01 a b c d e f Matsumura Shuichi Okamoto Kyoko 1997 12 01 Factors Affecting Proximity Among Members of a Wild Group of Moor Macaques During Feeding Moving and Resting International Journal of Primatology 18 6 929 940 doi 10 1023 A 1026344129760 ISSN 1573 8604 S2CID 45107000 a b c Beltran Frances Victor Castellano Navarro Alba Illa Maulany Risma Ngakan Putu O MacIntosh Andrew J J Llorente Miquel Amici Federica 2020 09 03 Play behavior in immature moor macaques Macaca maura and Japanese macaques Macaca fuscata American Journal of Primatology 82 10 e23192 doi 10 1002 ajp 23192 ISSN 1098 2345 PMID 32882065 S2CID 221496191 File Macaca maura groupe jpg Wikimedia Commons commons wikimedia org Retrieved 2022 12 01 a b c d e Morrow Kristen S Glanz Hunter Ngakan Putu Oka Riley Erin P December 2019 Interactions with humans are jointly influenced by life history stage and social network factors and reduce group cohesion in moor macaques Macaca maura Scientific Reports 9 1 20162 Bibcode 2019NatSR 920162M doi 10 1038 s41598 019 56288 z ISSN 2045 2322 PMC 6934674 PMID 31882849 Hernandez Tienda Clara Majolo Bonaventura Romero Teresa Illa Maulany Risma Oka Ngakan Putu Beltran Frances Victor Gregorio Hernandez Elisa Gomez Melara Jose Llorente Miquel Amici Federica 2022 04 01 The Habituation Process in Two Groups of Wild Moor Macaques Macaca maura International Journal of Primatology 43 2 291 316 doi 10 1007 s10764 021 00275 7 ISSN 1573 8604 PMC 8758468 PMID 35043025 Campbell Smith Gail Simanjorang Hubert V P Leader Williams Nigel Linkie Matthew 2010 Local attitudes and perceptions toward crop raiding by orangutans Pongo abelii and other nonhuman primates in northern Sumatra Indonesia American Journal of Primatology 72 10 866 876 doi 10 1002 ajp 20822 PMID 20301138 S2CID 5757864 Estrada Alejandro Raboy Becky E Oliveira Leonardo C 2012 Agroecosystems and Primate Conservation in the Tropics A Review American Journal of Primatology 74 8 696 711 doi 10 1002 ajp 22033 PMID 22605526 S2CID 205329975 Riley Erin P Priston Nancy E C 2010 Macaques in farms and folklore Exploring the human nonhuman primate interface in Sulawesi Indonesia American Journal of Primatology 72 10 848 854 doi 10 1002 ajp 20798 PMID 20146249 S2CID 23446462 External links edit nbsp Wikispecies has information related to Moor macaque Photos at ARKive Retrieved from https en wikipedia org w index php title Moor macaque amp oldid 1223196167, wikipedia, wiki, book, books, library,

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