Mandrill: Difference between revisions
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| status = VU | | status = VU | ||
| status_system = IUCN3.1 | | status_system = IUCN3.1 | ||
| status_ref = <ref name=iucn>{{cite iucn|author=Abernethy, K.|author2=Maisels, F.|date=2019|title=''Mandrillus sphinx''| | | status_ref = <ref name=iucn>{{cite iucn|author=Abernethy, K.|author2=Maisels, F.|date=2019|title=''Mandrillus sphinx''|article-number=e.T12754A17952325|doi=10.2305/IUCN.UK.2019-3.RLTS.T12754A17952325.en|access-date=19 November 2021}}</ref> | ||
| status2 = CITES_A1 | | status2 = CITES_A1 | ||
| status2_system = CITES | | status2_system = CITES | ||
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The mandrill was first scientifically depicted in ''[[Historia animalium (Gessner book)|Historia animalium]]'' (1551–1558) by [[Conrad Gessner]], who considered it a kind of [[hyena]].{{sfn|Dixson|2015|p=3}} The species was formally classified by [[Carl Linnaeus]] as ''Simia sphinx'' in 1758. Its current generic name ''[[Mandrillus]]'' was coined by [[Ferdinand August Maria Franz von Ritgen|Ferdinand Ritgen]] in 1824.<ref>{{cite book|author=Groves, Colin P.|contribution=Primates; Simiiformes; Catarrhini; Cercopithecoidea; Cercopithecidae; Cercopithecinae|title=Mammal Species of the World: A Taxonomic and Geographic Reference. Volume 1|publisher=Johns Hopkins University Press|year=1982|page=162|editor1=Wilson, Don E.|editor2=Reeder, DeeAnn M.|isbn=0-8018-8221-4|url=https://books.google.com/books?id=JgAMbNSt8ikC&dq=simia+sphinx+linnaeus&pg=PA165}}</ref> | The mandrill was first scientifically depicted in ''[[Historia animalium (Gessner book)|Historia animalium]]'' (1551–1558) by [[Conrad Gessner]], who considered it a kind of [[hyena]].{{sfn|Dixson|2015|p=3}} The species was formally classified by [[Carl Linnaeus]] as ''Simia sphinx'' in 1758. Its current generic name ''[[Mandrillus]]'' was coined by [[Ferdinand August Maria Franz von Ritgen|Ferdinand Ritgen]] in 1824.<ref>{{cite book|author=Groves, Colin P.|contribution=Primates; Simiiformes; Catarrhini; Cercopithecoidea; Cercopithecidae; Cercopithecinae|title=Mammal Species of the World: A Taxonomic and Geographic Reference. Volume 1|publisher=Johns Hopkins University Press|year=1982|page=162|editor1=Wilson, Don E.|editor2=Reeder, DeeAnn M.|isbn=0-8018-8221-4|url=https://books.google.com/books?id=JgAMbNSt8ikC&dq=simia+sphinx+linnaeus&pg=PA165}}</ref> | ||
Historically, some scientists placed the mandrill and the closely related [[Drill (animal)|drill]] (''M. leucophaeus'') in the baboon genus ''[[Papio]]''. [[Morphology (biology)|Morphological]] and [[Genetic analysis|genetic studies]] in the late 20th and early 21st centuries found a closer relationship to [[white-eyelid mangabey]]s of the genus ''Cercocebus''. Some have even proposed that the mandrill and drill belong to ''Cercocebus''.{{sfn|Dixson|2015|pp=6–7}} Two genetic studies in 2011 clarified ''Mandrillus'' and ''Cercocebus'' as separate [[Sister group|sister lineages]].<ref name=molecular>{{cite journal|author1=Perelman, P.|author2=Johnson, W. E.|author3=Roos, C.|author4=Seuánez, H. N.|author5=Horvath, J. E.|display-authors=etal|year=2011|title=A molecular phylogeny of living primates|journal=PLOS Genetics|volume=7|issue=3| | Historically, some scientists placed the mandrill and the closely related [[Drill (animal)|drill]] (''M. leucophaeus'') in the baboon genus ''[[Papio]]''. [[Morphology (biology)|Morphological]] and [[Genetic analysis|genetic studies]] in the late 20th and early 21st centuries found a closer relationship to [[white-eyelid mangabey]]s of the genus ''Cercocebus''. Some have even proposed that the mandrill and drill belong to ''Cercocebus''.{{sfn|Dixson|2015|pp=6–7}} Two genetic studies in 2011 clarified ''Mandrillus'' and ''Cercocebus'' as separate [[Sister group|sister lineages]].<ref name=molecular>{{cite journal|author1=Perelman, P.|author2=Johnson, W. E.|author3=Roos, C.|author4=Seuánez, H. N.|author5=Horvath, J. E.|display-authors=etal|year=2011|title=A molecular phylogeny of living primates|journal=PLOS Genetics|volume=7|issue=3|article-number=e1001342|doi=10.1371/journal.pgen.1001342|pmid=21436896|pmc=3060065 |doi-access=free }}</ref><ref name=mitogenome>{{cite journal|author1=Finstermeier, K.|author2=Zinner, D.|author3=Brameier, M.|author4=Meyer, M.|author5=Kreuz, E.|display-authors=etal|year=2011|title=A mitogenomic phylogeny of living primates|journal=PLOS ONE|volume=8|issue=7|article-number=e69504|doi=10.1371/journal.pone.0069504|pmid=23874967|pmc=3713065|doi-access=free}}</ref> The two genera [[Split (phylogenetics)|split]] around 4.5 million years ago (mya) while the mandrill and drill split approximately 3.17 mya. Fossils of ''Mandrillus'' have not been found.{{sfn|Dixson|2015|pp=13–15, 133}} | ||
{{clade gallery |width=225px |height=200px | {{clade gallery |width=225px |height=200px | ||
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==Characteristics== | ==Characteristics== | ||
[[File:Mandrilperspective6.jpg|thumb|left|upright|Skull of male mandrill, showing the long canines and ridged bone swellings|alt=Skull of male mandrill, showing the long canines and ridged bone swellings]] | [[File:Mandrilperspective6.jpg|thumb|left|upright|Skull of male mandrill, showing the long canines and ridged bone swellings|alt=Skull of male mandrill, showing the long canines and ridged bone swellings]] | ||
The mandrill has a stocky body with a large head and muzzle, as well as a short and stumpy tail.{{sfn|Dixson|2015|p=16}} The limbs are evenly sized and the fingers and toes are more elongated than those in baboons,<ref name="Ankel-Simons 2007 ">{{cite book|last=Ankel-Simons |first=F. |year=2007 |title=Primate Anatomy: An Introduction|edition=3rd|publisher=Elsevier Academic Press |isbn=978-0-08-046911-9 |url=https://books.google.com/books?id=Mwl3M6c5KzoC&q=%22Mandrill%22|page=128}}</ref> with a more opposable big toe on the feet.{{sfn|Dixson|2015|p=23}} The mandrill is the most [[sexually dimorphic]] primate,<ref name="Leigh 2008"/> and it is the largest [[monkey]].{{sfn|Dixson|2015|p=114}} Females are less stocky and have shorter, flatter snouts.{{sfn|Dixson|2015|p=16}} Males have a {{cvt|70|–|95|cm}} head-body length and weigh {{cvt|19|–|30|kg}} while females have a {{cvt|55|–|70|cm}} head-body length and weigh {{cvt|10|–|15|kg}}.<ref name=kingdon>{{cite book |author=Kingdon, J. |year=2015|title=The Kingdon Field Guide to African Mammals|publisher=Bloomsbury Publishing |page=129 |isbn=978-1-4729-1236-7}}</ref> Most of the teeth are larger in males,<ref>{{cite journal|author1=Dirks, W. |author2=Lemmers, S. A. M. |author3=Ngoubangoye, B. |author4=Herbert, A. |author5=Setchell, J. M. |year=2020 |title=Odontochronologies in male and female mandrills (''Mandrillus sphinx'') and the development of dental sexual dimorphism |journal=American Journal of Physical Anthropology |volume=172 |issue=4 |pages=528–544 |doi=10.1002/ajpa.24094 |pmid=32510604 |s2cid=219539657|doi-access=free}}</ref> and the canine teeth reach up to {{cvt|4.5|cm}} and {{cvt|1|cm}} long for males and females respectively.<ref name="Leigh 2008">{{cite journal |author1=Leigh, S. R.|author2=Setchell, J. M. |author3=Charpentier, M. |author4=Knapp, L. A. |author5=Wickings, E. J. |pmid=18472142 |year=2008|title=Canine tooth size and fitness in male mandrills (''Mandrillus sphinx'') |volume=55|issue=1|pages=75–85 |doi=10.1016/j.jhevol.2008.01.001 |journal=Journal of Human Evolution|bibcode=2008JHumE..55...75L }}</ref> Both sexes have {{cvt|7|–|10|cm}} long tails.<ref name=kingdon/> | The mandrill has a stocky body with a large head and muzzle, as well as a short and stumpy tail.{{sfn|Dixson|2015|p=16}} The limbs are evenly sized and the fingers and toes are more elongated than those in baboons,<ref name="Ankel-Simons 2007">{{cite book|last=Ankel-Simons |first=F. |year=2007 |title=Primate Anatomy: An Introduction|edition=3rd|publisher=Elsevier Academic Press |isbn=978-0-08-046911-9 |url=https://books.google.com/books?id=Mwl3M6c5KzoC&q=%22Mandrill%22|page=128}}</ref> with a more opposable big toe on the feet.{{sfn|Dixson|2015|p=23}} The mandrill is the most [[sexually dimorphic]] primate,<ref name="Leigh 2008"/> and it is the largest [[monkey]].{{sfn|Dixson|2015|p=114}} Females are less stocky and have shorter, flatter snouts.{{sfn|Dixson|2015|p=16}} Males have a {{cvt|70|–|95|cm}} head-body length and weigh {{cvt|19|–|30|kg}} while females have a {{cvt|55|–|70|cm}} head-body length and weigh {{cvt|10|–|15|kg}}.<ref name=kingdon>{{cite book |author=Kingdon, J. |year=2015|title=The Kingdon Field Guide to African Mammals|publisher=Bloomsbury Publishing |page=129 |isbn=978-1-4729-1236-7}}</ref> Most of the teeth are larger in males,<ref>{{cite journal|author1=Dirks, W. |author2=Lemmers, S. A. M. |author3=Ngoubangoye, B. |author4=Herbert, A. |author5=Setchell, J. M. |year=2020 |title=Odontochronologies in male and female mandrills (''Mandrillus sphinx'') and the development of dental sexual dimorphism |journal=American Journal of Physical Anthropology |volume=172 |issue=4 |pages=528–544 |doi=10.1002/ajpa.24094 |pmid=32510604 |bibcode=2020AJPA..172..528D |s2cid=219539657|doi-access=free}}</ref> and the canine teeth reach up to {{cvt|4.5|cm}} and {{cvt|1|cm}} long for males and females respectively.<ref name="Leigh 2008">{{cite journal |author1=Leigh, S. R.|author2=Setchell, J. M. |author3=Charpentier, M. |author4=Knapp, L. A. |author5=Wickings, E. J. |pmid=18472142 |year=2008|title=Canine tooth size and fitness in male mandrills (''Mandrillus sphinx'') |volume=55|issue=1|pages=75–85 |doi=10.1016/j.jhevol.2008.01.001 |journal=Journal of Human Evolution|bibcode=2008JHumE..55...75L |url=https://durham-repository.worktribe.com/output/1530435 }}</ref> Both sexes have {{cvt|7|–|10|cm}} long tails.<ref name=kingdon/> | ||
[[File:Mandrils (36370557765).jpg|thumb|upright=1|Male and female mandrills, showing size and color dimorphism|alt=Male and female mandrill sitting down]] | [[File:Mandrils (36370557765).jpg|thumb|upright=1|Male and female mandrills, showing size and color dimorphism|alt=Male and female mandrill sitting down]] | ||
The [[animal coat|coat]] of the mandrill is primarily grizzled or [[Agouti (coloration)|banded]] olive-brown with a yellow-orange beard and sparse, light hairs on its underside.{{sfn|Dixson|2015|p=16}}<ref name=kingdon/> The lips are surrounded by stiff white [[whiskers]], and white bare skin exists behind the ears. Male mandrills have a "crest" of long hairs on the head and neck, while both sexes have chest glands which are covered by long hairs. The face, rump and genitals have less hair.{{sfn|Dixson|2015|pp=16–17}} The mandrill has a red line running down the middle of their face which connects to their red nose. On either side of the line, the skin is blue and grooved.<ref name=kingdon/>{{sfn|Dixson|2015|p=17}} In males, the blue skin is supported by ridged bone swellings. Females have more subdued facial coloring, but this can vary between individuals with some having stronger red and blue hues and others being darker or almost black.{{sfn|Dixson|2015|pp=17–18}} In males, the rump and areas around the genitals are multi-colored, consisting of red, pink, blue and purple skin,<ref name="Ankel-Simons 2007 "/>{{sfn|Dixson|2015|pp=17–18}} with a red penis shaft and violet scrotum. The genital and anal areas of the female are red.{{sfn|Dixson|2015|pp=17–19}} | The [[animal coat|coat]] of the mandrill is primarily grizzled or [[Agouti (coloration)|banded]] olive-brown with a yellow-orange beard and sparse, light hairs on its underside.{{sfn|Dixson|2015|p=16}}<ref name=kingdon/> The lips are surrounded by stiff white [[whiskers]], and white bare skin exists behind the ears. Male mandrills have a "crest" of long hairs on the head and neck, while both sexes have chest glands which are covered by long hairs. The face, rump and genitals have less hair.{{sfn|Dixson|2015|pp=16–17}} The mandrill has a red line running down the middle of their face which connects to their red nose. On either side of the line, the skin is blue and grooved.<ref name=kingdon/>{{sfn|Dixson|2015|p=17}} In males, the blue skin is supported by ridged bone swellings. Females have more subdued facial coloring, but this can vary between individuals with some having stronger red and blue hues and others being darker or almost black.{{sfn|Dixson|2015|pp=17–18}} In males, the rump and areas around the genitals are multi-colored, consisting of red, pink, blue and purple skin,<ref name="Ankel-Simons 2007"/>{{sfn|Dixson|2015|pp=17–18}} with a red penis shaft and violet scrotum. The genital and anal areas of the female are red.{{sfn|Dixson|2015|pp=17–19}} | ||
The mandrill is among the most colorful mammals. [[Charles Darwin]] wrote in ''[[The Descent of Man]]'': "no other member of the whole class of mammals is coloured in so extraordinary a manner as the adult male mandrill".<ref>{{cite book|last=Darwin|first=C. |author-link=Charles Darwin |year=1871|title=The Descent of Man, and Selection in Relation to Sex|publisher=[[John Murray (publishing house)|John Murray]] |oclc=39301709 |page=292 |url=https://archive.org/details/bub_gb_Na9LAAAAMAAJ/page/n303}}</ref> The red coloration is created by blood vessels near the surface of the skin,<ref name="Setchell 2001" /> while the blue is a form of [[structural coloration]] caused by parallel arrangements of [[collagen]] fibers.<ref name=Prum2004>{{Cite journal|last1=Prum|first1=R. O.|last2=Torres|first2=R. H. |year=2004 |title=Structural colouration of mammalian skin: Convergent evolution of coherently scattering dermal collagen arrays |journal=Journal of Experimental Biology |volume=207 |issue=12|pages=2157–2172 |doi=10.1242/jeb.00989 |pmid=15143148|s2cid=8268610|doi-access=free |url=https://kuscholarworks.ku.edu/bitstream/1808/1599/1/2157.pdf}}</ref> The blue ridges on males contrast with both the red facial hues and the green foliage of their environment, helping them stand out to other individuals.<ref name="Renoult 2011">{{Cite journal|doi=10.1371/journal.pone.0029117|pmid=22216180|pmc=3244440|title=The evolution of the multicoloured face of mandrills: Insights from the perceptual space of colour vision|journal=PLOS ONE |volume=6 |issue=12 | | The mandrill is among the most colorful mammals. [[Charles Darwin]] wrote in ''[[The Descent of Man]]'': "no other member of the whole class of mammals is coloured in so extraordinary a manner as the adult male mandrill".<ref>{{cite book|last=Darwin|first=C. |author-link=Charles Darwin |year=1871|title=The Descent of Man, and Selection in Relation to Sex|publisher=[[John Murray (publishing house)|John Murray]] |oclc=39301709 |page=292 |url=https://archive.org/details/bub_gb_Na9LAAAAMAAJ/page/n303}}</ref> The red coloration is created by blood vessels near the surface of the skin,<ref name="Setchell 2001" /> while the blue is a form of [[structural coloration]] caused by parallel arrangements of [[collagen]] fibers.<ref name=Prum2004>{{Cite journal|last1=Prum|first1=R. O.|last2=Torres|first2=R. H. |year=2004 |title=Structural colouration of mammalian skin: Convergent evolution of coherently scattering dermal collagen arrays |journal=Journal of Experimental Biology |volume=207 |issue=12|pages=2157–2172 |doi=10.1242/jeb.00989 |pmid=15143148|bibcode=2004JExpB.207.2157P |s2cid=8268610|doi-access=free |url=https://kuscholarworks.ku.edu/bitstream/1808/1599/1/2157.pdf}}</ref> The blue ridges on males contrast with both the red facial hues and the green foliage of their environment, helping them stand out to other individuals.<ref name="Renoult 2011">{{Cite journal|doi=10.1371/journal.pone.0029117|pmid=22216180|pmc=3244440|title=The evolution of the multicoloured face of mandrills: Insights from the perceptual space of colour vision|journal=PLOS ONE |volume=6 |issue=12 |article-number=e29117 |year=2011 |last1=Renoult|first1=J. P.|last2=Schaefer|first2=H. M. |last3=Sallé |first3=B. |last4=Charpentier |first4=M. J. E. |bibcode=2011PLoSO...629117R |doi-access=free}}</ref> The darker and more subdued coloring of female faces is caused by [[melanin]].{{sfn|Dixson|2015|p=18}} | ||
==Ecology== | ==Ecology== | ||
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The mandrill lives in west-central Africa, including southern [[Cameroon]], mainland [[Equatorial Guinea]] ([[Río Muni]]), [[Gabon]] and parts of the [[Republic of the Congo]]. Its range is bounded by the [[Sanaga River]] to the north and the Ogooué and [[Ivindo River]]s to the east. It does not appear to [[Sympatry|share habitat]] with the drill, as the two species are separated by the Sanaga River.{{sfn|Dixson|2015|pp=9–11}} Mandrills live in [[tropical rainforest]]s, generally preferring [[Old-growth forest|primary forest]]s over [[secondary forest]]s. They also live in patchy [[gallery forest]]s surrounded by [[savanna]] and travel across grass areas within their forest habitats.<ref name="Harrison 1988">{{cite journal|author=Harrison, M. J. S.|title=The mandrill in Gabon's rain forest-ecology, distribution and status|doi=10.1017/S0030605300022365|year=2009|journal=Oryx|volume=22|issue=4|pages=218–228|doi-access=free}}</ref> They have also been recorded in mountainous areas, near rivers and in [[Horticulture|cultivated fields]].<ref name="Sabater Pi J 1972">{{cite journal|author=Sabater Pi, J.|author-link=Jordi Sabater Pi|pmid=4624917|title=Contribution to the ecology of ''Mandrillus sphinx'' Linnaeus 1758 of Rio Muni (Republic of Equatorial Guinea)|year=1972|volume=17|issue=4|pages=304–319|journal=Folia Primatologica|doi=10.1159/000155442}}</ref> | The mandrill lives in west-central Africa, including southern [[Cameroon]], mainland [[Equatorial Guinea]] ([[Río Muni]]), [[Gabon]] and parts of the [[Republic of the Congo]]. Its range is bounded by the [[Sanaga River]] to the north and the Ogooué and [[Ivindo River]]s to the east. It does not appear to [[Sympatry|share habitat]] with the drill, as the two species are separated by the Sanaga River.{{sfn|Dixson|2015|pp=9–11}} Mandrills live in [[tropical rainforest]]s, generally preferring [[Old-growth forest|primary forest]]s over [[secondary forest]]s. They also live in patchy [[gallery forest]]s surrounded by [[savanna]] and travel across grass areas within their forest habitats.<ref name="Harrison 1988">{{cite journal|author=Harrison, M. J. S.|title=The mandrill in Gabon's rain forest-ecology, distribution and status|doi=10.1017/S0030605300022365|year=2009|journal=Oryx|volume=22|issue=4|pages=218–228|doi-access=free}}</ref> They have also been recorded in mountainous areas, near rivers and in [[Horticulture|cultivated fields]].<ref name="Sabater Pi J 1972">{{cite journal|author=Sabater Pi, J.|author-link=Jordi Sabater Pi|pmid=4624917|title=Contribution to the ecology of ''Mandrillus sphinx'' Linnaeus 1758 of Rio Muni (Republic of Equatorial Guinea)|year=1972|volume=17|issue=4|pages=304–319|journal=Folia Primatologica|doi=10.1159/000155442}}</ref> | ||
Mandrills prefer thick bush dominated by [[perennial plant]]s like [[Zingiberaceae|ginger]]s and plants of the genera ''[[Brillantaisia]]'' and ''[[Phaulopsis]]''.<ref name=kingdon/><ref name="Sabater Pi J 1972" /> They mainly dwell on the ground, but feed as high as the [[Canopy (biology)|canopy]].<ref name="Harrison 1988"/> Both mandrills and drills are more [[Arboreal locomotion|arboreal]] than baboons.<ref name="Ankel-Simons 2007 "/> Mandrills may aggregate or compete with other primates such as [[talapoin]]s, [[guenon]]s, mangabeys, [[black-and-white colobus]]es, [[chimpanzee]]s, and [[gorilla]]s.<ref name="Harrison 1988"/><ref name="Sabater Pi J 1972" /> | Mandrills prefer thick bush dominated by [[perennial plant]]s like [[Zingiberaceae|ginger]]s and plants of the genera ''[[Brillantaisia]]'' and ''[[Phaulopsis]]''.<ref name=kingdon/><ref name="Sabater Pi J 1972" /> They mainly dwell on the ground, but feed as high as the [[Canopy (biology)|canopy]].<ref name="Harrison 1988"/> Both mandrills and drills are more [[Arboreal locomotion|arboreal]] than baboons.<ref name="Ankel-Simons 2007"/> Mandrills may aggregate or compete with other primates such as [[talapoin]]s, [[guenon]]s, mangabeys, [[black-and-white colobus]]es, [[chimpanzee]]s, and [[gorilla]]s.<ref name="Harrison 1988"/><ref name="Sabater Pi J 1972" /> | ||
=== | ===Diet=== | ||
[[File:Parc zoo limbe69.jpg|thumb|Mandrills eating fruit|alt=Mandrills behind a fence eating fruit]] | [[File:Parc zoo limbe69.jpg|thumb|Mandrills eating fruit|alt=Mandrills behind a fence eating fruit]] | ||
The mandrill's preferred fruits include those of the [[Anacardiaceae|cashew]] species ''[[Pseudospondias microcarpa]]'', the [[Rubiaceae|coffee]] species ''[[Nauclea diderrichii]]'' and the [[Hypericaceae|wort]] species ''[[Psorospermum febrifugum]]''.<ref name="Rogers 1996"/> Mandrills consume more seeds than many other primate species.<ref name="Hoshino 1985" | The mandrill is an [[omnivore]]. The core of its diet consists of plants, of which it eats over a hundred species.<ref name="Hoshino 1985">{{cite journal |author=Hoshino, J. |title=Feeding ecology of mandrills (''Mandrillus sphinx'') in Campo Animal Reserve, Cameroon |doi=10.1007/BF02382401|year=1985|journal=Primates|volume=26|issue=3|pages=248–273|s2cid=12216632}}</ref> In [[Lopé National Park]], the mandrill's diet was composed of fruit (50.7%), seeds (26.0%), leaves (8.2%), [[pith]] (6.8%), flowers (2.7%), and animal matter (4.1%), with other foods making up the remaining 1.4%.<ref name=Tutin1997>{{cite journal|author1=Tutin, C. E. |author2=Ham, R. M. |author3=White, L. J.|author4=Harrison, M. J. |pmid=9108968 |title=The primate community of the Lopé Reserve, Gabon: diets, responses to fruit scarcity, and effects on biomass |year=1997|volume=42|issue=1|pages=1–24|doi=10.1002/(SICI)1098-2345(1997)42:1<1::AID-AJP1>3.0.CO;2-0 |journal=American Journal of Primatology|s2cid=37902903}}</ref> During the wet season, mandrills forage in continuous forest, when fruit is most available, while during the dry season they feed in gallery forests and at the borders of savannas and forests.<ref name="Rogers 1996"/> | ||
The mandrill's preferred fruits include those of the [[Anacardiaceae|cashew]] species ''[[Pseudospondias microcarpa]]'', the [[Rubiaceae|coffee]] species ''[[Nauclea diderrichii]]'' and the [[Hypericaceae|wort]] species ''[[Psorospermum febrifugum]]''.<ref name="Rogers 1996"/> Mandrills consume more seeds than many other primate species.<ref name="Hoshino 1985"/> Adult male mandrills are one of the few primates capable of biting through the hard shell of ''[[Detarium microcarpum]]'' seeds.<ref name=Tutin1997/> For vegetation, they mostly eat the young leaves, shoots and piths of [[monocot]] plants.<ref name="Hoshino 1985"/> In particular, mandrills consume leaves from the [[Marantaceae|arrowroots]] ''[[Haumania liebrechtsiana]]'' and ''[[Trachyphrynium braunianum]]'', as well as the piths of ginger plants like ''[[Renealmia macrocolia]]'' and species in the genus ''[[Aframomum]]''.<ref name="Rogers 1996"/> They are also known to consume mushrooms.<ref name="Hoshino 1985"/> | |||
The rest of a mandrill's diet is largely made up of invertebrates, particularly [[ant]]s, [[termite]]s, [[Cricket (insect)|cricket]]s, [[spider]]s, [[snail]]s, and [[scorpion]]s. They also eat birds and their eggs, frogs and rodents.<ref name="Hoshino 1985" /><ref name="Kudo 1985"/> Mandrills have been recorded preying on larger vertebrates such as juvenile [[Bay Duiker|bay duiker]]s. Such prey is killed with a bite to the head followed by pulling off the hind limbs and tearing open the belly. Individuals may cooperate during hunting and share kills.<ref name="Kudo 1985">{{cite journal|author1=Kudo, H.|author2=Mitani, M.|title=New record of predatory behavior by the mandrill in Cameroon|doi=10.1007/BF02382015|year=1985|journal=Primates|volume=26|issue=2|pages=161–167|s2cid=20928597}}</ref> | The rest of a mandrill's diet is largely made up of invertebrates, particularly [[ant]]s, [[termite]]s, [[Cricket (insect)|cricket]]s, [[spider]]s, [[snail]]s, and [[scorpion]]s. They also eat birds and their eggs, frogs and rodents.<ref name="Hoshino 1985"/><ref name="Kudo 1985"/> Mandrills have been recorded preying on larger vertebrates such as juvenile [[Bay Duiker|bay duiker]]s. Such prey is killed with a bite to the head followed by pulling off the hind limbs and tearing open the belly. Individuals may cooperate during hunting and share kills.<ref name="Kudo 1985">{{cite journal |author1=Kudo, H.|author2=Mitani, M.|title=New record of predatory behavior by the mandrill in Cameroon |doi=10.1007/BF02382015 |year=1985|journal=Primates|volume=26|issue=2|pages=161–167 |s2cid=20928597}}</ref> | ||
===Predators, parasites and pathogens=== | ===Predators, parasites and pathogens=== | ||
[[Leopard]]s may prey on mandrills, as traces of mandrill have been found in their feces.<ref name= Henschel>{{cite journal|last1=Henschel|first1=P.|last2=Abernethy|first2=K. A.|last3=White|first3=L. J. T.|year=2005|title=Leopard food habits in the Lopé National Park, Gabon, Central Africa|journal=African Journal of Ecology|volume=43|issue=1|pages=21–28|doi=10.1111/j.1365-2028.2004.00518.x|bibcode=2005AfJEc..43...21H }}</ref> Other potential predators include [[African rock python]]s, [[crowned eagle]]s and chimpanzees.<ref name="Harrison 1988"/>{{sfn|Dixson|2015|p=71}} Leopards are a threat to all individuals, while eagles are only threats to the young.<ref name="Yorzinski 2008"/>{{sfn|Dixson|2015|p=71}} In a study where a mandrill group was exposed to models of leopards and crown eagles, the leopard models tended to cause the mandrills to flee up trees while the eagles were more likely to drive them to take cover. The dominant male did not flee from either model types; in the case of the leopards, he paced around while looking in their direction. [[Alarm signal|Alarm call]]s were more commonly heard in response to leopards than eagles.<ref name="Yorzinski 2008">{{cite journal|author1=Yorzinski, J. L.|author2=Vehrencamp, S. L.|year=2008|title=Preliminary report: antipredator behaviors of mandrills|journal=Primate Report|volume=75|pages=11–18|url=https://yorzinskilab.org/wp-content/uploads/2021/02/yorzinskivehrencamp_2008.pdf}}</ref> | [[Leopard]]s may prey on mandrills, as traces of mandrill have been found in their feces.<ref name= Henschel>{{cite journal|last1=Henschel|first1=P.|last2=Abernethy|first2=K. A.|last3=White|first3=L. J. T.|year=2005|title=Leopard food habits in the Lopé National Park, Gabon, Central Africa|journal=African Journal of Ecology|volume=43|issue=1|pages=21–28|doi=10.1111/j.1365-2028.2004.00518.x|bibcode=2005AfJEc..43...21H }}</ref> Other potential predators include [[African rock python]]s, [[crowned eagle]]s and chimpanzees.<ref name="Harrison 1988"/>{{sfn|Dixson|2015|p=71}} Leopards are a threat to all individuals, while eagles are only threats to the young.<ref name="Yorzinski 2008"/>{{sfn|Dixson|2015|p=71}} In a study where a mandrill group was exposed to models of leopards and crown eagles, the leopard models tended to cause the mandrills to flee up trees while the eagles were more likely to drive them to take cover. The dominant male did not flee from either model types; in the case of the leopards, he paced around while looking in their direction. [[Alarm signal|Alarm call]]s were more commonly heard in response to leopards than eagles.<ref name="Yorzinski 2008">{{cite journal|author1=Yorzinski, J. L.|author2=Vehrencamp, S. L.|year=2008|title=Preliminary report: antipredator behaviors of mandrills|journal=Primate Report|volume=75|pages=11–18|url=https://yorzinskilab.org/wp-content/uploads/2021/02/yorzinskivehrencamp_2008.pdf}}</ref> | ||
Mandrills can become infected with gastrointestinal parasites, such as [[nematode]]s and [[protozoa]]. [[Cordylobia anthropophaga|Tumbu fly]] larvae may live under the skin and individuals that walk | Mandrills can become infected with gastrointestinal parasites, such as [[nematode]]s and [[protozoa]]. [[Cordylobia anthropophaga|Tumbu fly]] larvae may live under the skin and individuals that walk through grassland can get infested with [[tick]]s. Blood parasites include the [[malaria]]-causing ''[[Plasmodium]]'' and the nematode ''[[Loa loa]]'', which is transmitted by bites from [[deer fly|deer flies]].{{sfn|Dixson|2015|pp=71–73}} Wild mandrills have tested positive for SIV, [[enterovirus]]es of the species [[Enterovirus#Taxonomy|EV-J]] and [[astrovirus]]es, including a human variant.<ref name=Telfer/><ref>{{cite journal|author1=Mombo, I. M.|author2=Boundenga, L.|author3=Suquet, E.|display-authors=etal|year=2021|title=Natural infection of free-ranging mandrills (''Mandrillus sphinx'') by enteroviruses and astroviruses in southern Gabon|journal=Microbial Pathogenesis|volume=150|article-number=104659|doi=10.1016/j.micpath.2020.104659|pmid=33249166|s2cid=227236595}}</ref> | ||
==Behavior and life history== | ==Behavior and life history== | ||
| Line 122: | Line 122: | ||
Mandrills live in large "supergroups" or "hordes" that can contain hundreds of individuals.<ref name="Rogers 1996"/>{{sfn|Dixson|2015|pp=35–36}}<ref name="Abernethy 2002"/> These large groups are fairly stable and do not appear to be gatherings of smaller ones. At [[Lopé National Park]], Gabon, mandrill hordes were found to have an average of 620 individuals, and some groups were as large as 845, making them possibly the largest cohesive groups of wild primates.<ref name="Abernethy 2002">{{cite journal|author1=Abernethy, K. A.|author2=White, L. J. T.|author3=Wickings, E. J.|year=2002|title=Hordes of mandrills (''Mandrillus sphinx''): extreme group size and seasonal male presence|journal=Journal of Zoology|volume=258|issue=1|pages=131–137|doi=10.1017/S0952836902001267|hdl=1893/21013|url=http://dspace.stir.ac.uk/bitstream/1893/21013/1/Abernethy.J.Zool.Lond.v258.p131.%202002.pdf}}</ref> Another study in Lopé found that a horde of 625 mandrills consisted of 21 dominant males, 71 less dominant and subadult males, 247 adult and adolescent females, 200 juveniles, and 86 dependent infants.<ref name="Rogers 1996">{{cite journal|author=Rogers, M. E.|author2=Abernethy, K. A.|author3=Fontaine, B.|author4=Wickings, E. J.|author5=White, L. J. T.|author6=Tutin, C. E. G.|title=Ten days in the life of a mandrill horde in the Lopé Reserve, Gabon|doi=10.1002/(SICI)1098-2345(1996)40:4<297::AID-AJP1>3.0.CO;2-T|pmid=31918520|year=1996|journal=American Journal of Primatology|volume=40|issue=4|pages=297–313|s2cid=85028393}}</ref> A mandrill horde of around 700 individuals in northern Lopé had a total [[home range]] of {{convert|182|km2|abbr=on}}, {{convert|89|km2|abbr=on}} of which was suitable habitat. The supergroup would occasionally diverge into two to four subgroups before reuniting.<ref>{{cite journal|author1=White, E. C.|author2=Dikangadissi, J.-T.|author3=Dimoto, E.|display-authors=etal|year=2010|title=Home-range use by a large horde of wild ''Mandrillus sphinx''|journal=International Journal of Primatology|volume=31|issue=4|pages=627–645|doi=10.1007/s10764-010-9417-3|s2cid=44740032}}</ref> Another 15-month long study of a 120-member group found a home range of {{convert|8.6|km2|abbr=on}} with an average traveling distance of {{convert|2.42|km|abbr=on}} per day.<ref name=Brockmeyer2015>{{cite journal|author1=Brockmeyer, T.|author2=Kappeler, P. M.|author3=Willaume, E.|author4=Benoit, L.|author5=Mboumba, S.|author6=Charpentier, M. J. E.|year=2015|title=Social organization and space use of a wild mandrill (''Mandrillus sphinx'') group|journal=American Journal of Primatology|volume=77|issue=10|pages=1036–1048|doi=10.1002/ajp.22439|pmid=26235675|s2cid=38327403}}</ref> | Mandrills live in large "supergroups" or "hordes" that can contain hundreds of individuals.<ref name="Rogers 1996"/>{{sfn|Dixson|2015|pp=35–36}}<ref name="Abernethy 2002"/> These large groups are fairly stable and do not appear to be gatherings of smaller ones. At [[Lopé National Park]], Gabon, mandrill hordes were found to have an average of 620 individuals, and some groups were as large as 845, making them possibly the largest cohesive groups of wild primates.<ref name="Abernethy 2002">{{cite journal|author1=Abernethy, K. A.|author2=White, L. J. T.|author3=Wickings, E. J.|year=2002|title=Hordes of mandrills (''Mandrillus sphinx''): extreme group size and seasonal male presence|journal=Journal of Zoology|volume=258|issue=1|pages=131–137|doi=10.1017/S0952836902001267|hdl=1893/21013|url=http://dspace.stir.ac.uk/bitstream/1893/21013/1/Abernethy.J.Zool.Lond.v258.p131.%202002.pdf}}</ref> Another study in Lopé found that a horde of 625 mandrills consisted of 21 dominant males, 71 less dominant and subadult males, 247 adult and adolescent females, 200 juveniles, and 86 dependent infants.<ref name="Rogers 1996">{{cite journal|author=Rogers, M. E.|author2=Abernethy, K. A.|author3=Fontaine, B.|author4=Wickings, E. J.|author5=White, L. J. T.|author6=Tutin, C. E. G.|title=Ten days in the life of a mandrill horde in the Lopé Reserve, Gabon|doi=10.1002/(SICI)1098-2345(1996)40:4<297::AID-AJP1>3.0.CO;2-T|pmid=31918520|year=1996|journal=American Journal of Primatology|volume=40|issue=4|pages=297–313|s2cid=85028393}}</ref> A mandrill horde of around 700 individuals in northern Lopé had a total [[home range]] of {{convert|182|km2|abbr=on}}, {{convert|89|km2|abbr=on}} of which was suitable habitat. The supergroup would occasionally diverge into two to four subgroups before reuniting.<ref>{{cite journal|author1=White, E. C.|author2=Dikangadissi, J.-T.|author3=Dimoto, E.|display-authors=etal|year=2010|title=Home-range use by a large horde of wild ''Mandrillus sphinx''|journal=International Journal of Primatology|volume=31|issue=4|pages=627–645|doi=10.1007/s10764-010-9417-3|s2cid=44740032}}</ref> Another 15-month long study of a 120-member group found a home range of {{convert|8.6|km2|abbr=on}} with an average traveling distance of {{convert|2.42|km|abbr=on}} per day.<ref name=Brockmeyer2015>{{cite journal|author1=Brockmeyer, T.|author2=Kappeler, P. M.|author3=Willaume, E.|author4=Benoit, L.|author5=Mboumba, S.|author6=Charpentier, M. J. E.|year=2015|title=Social organization and space use of a wild mandrill (''Mandrillus sphinx'') group|journal=American Journal of Primatology|volume=77|issue=10|pages=1036–1048|doi=10.1002/ajp.22439|pmid=26235675|s2cid=38327403}}</ref> | ||
[[File:Artis Mandrill family - Artis Royal Zoo (10037453526).jpg|thumb|left|Mandrills grooming at [[Natura Artis Magistra]]]] | [[File:Artis Mandrill family - Artis Royal Zoo (10037453526).jpg|thumb|left|Mandrills grooming at [[Natura Artis Magistra]]]] | ||
Hordes consist of [[matrilineal]] family groups, and females are important for maintaining social cohesion. Strong connections with their relatives may lead to support during conflicts, higher survival rate of offspring and a longer lifespan for females. Dominant females are at the center of the group network and their removal leads to fewer social connections in the group.<ref>{{cite journal|author1=Bret, C.|author2=Sueur, C.|author3=Ngoubangoye, B.|author4=Verrier, D.|author5=Deneubourg, J.-L.|author6=Petit, O.|year=2013|title=Social structure of a semi-free ranging group of mandrills (''Mandrillus sphinx''): A social network analysis|journal=PLOS ONE|volume=8|issue=12| | Hordes consist of [[matrilineal]] family groups, and females are important for maintaining social cohesion. Strong connections with their relatives may lead to support during conflicts, higher survival rate of offspring and a longer lifespan for females. Dominant females are at the center of the group network and their removal leads to fewer social connections in the group.<ref>{{cite journal|author1=Bret, C.|author2=Sueur, C.|author3=Ngoubangoye, B.|author4=Verrier, D.|author5=Deneubourg, J.-L.|author6=Petit, O.|year=2013|title=Social structure of a semi-free ranging group of mandrills (''Mandrillus sphinx''): A social network analysis|journal=PLOS ONE|volume=8|issue=12|article-number=e83015|doi=10.1371/journal.pone.0083015|pmid=24340074|pmc=3858359|bibcode=2013PLoSO...883015B|doi-access=free}}</ref> The social rank of a mother mandrill can contribute to the social rank of both her female and male offspring.<ref name=Ontogeny/> Mature males are not permanent members of hordes but join as females become sexually receptive and leave as their sexual cycle ends. As a result, the coloration of the male mandrill may be intended to attract attention in a social structure with no long-term relationships between mates.<ref name="Abernethy 2002"/> Higher ranking males are found in the center of a social group while lower ranking males are more likely to occupy the periphery.<ref name=arresteddevelopment/> Females have some control over the males and coalitions can expel an unwanted male from a group.<ref>{{cite journal|author1=Setchell, J. M.|author2=Knapp, L. A.|author3=Wickings, E. J.|year=2006|title=Violent coalitionary attack by female mandrills against an injured alpha male|journal=American Journal of Primatology|volume=68|issue=4|pages=411–418|doi=10.1002/ajp.20234|pmid=16534806|s2cid=40486302 |url=https://durham-repository.worktribe.com/output/1541274 }}</ref> Outside the breeding season, males are believed to lead a solitary life and all-male [[Bachelor herd|bachelor groups]] are not known to exist.<ref name="Abernethy 2002"/> | ||
Both male and female mandrills rub and mark trees and branches with secretions from their chest glands, though males (and especially dominant males) mark more than females. The chemicals in the secretions signal the individual's sex, age and rank. Scent-marking may also serve a [[Territory (animal)|territorial]] function, captive alpha males will mark enclosure boundaries.<ref>{{cite journal|author1=Vaglio, S.|author2=Minicozzi, P.|author3=Romoli, R.|display-authors=etal|year=2016|title=Sternal gland scent-marking signals sex, age, rank, and group identity in captive mandrills|journal=Chemical Senses|volume=41|issue=2|pages=177–186|doi=10.1093/chemse/bjv077|pmid=26708734|doi-access=free|hdl=2436/601458|hdl-access=free}}</ref> Mandrills will [[Social grooming|groom]] one another, even when there is no benefit to be gained from doing so.<ref>{{Cite journal|url=https://link.springer.com/article/10.1007/s10764-010-9477-4|doi=10.1007/s10764-010-9477-4|title=Grooming and the expectation of reciprocation in mandrills (''Mandrillus sphinx'')|year=2011|last1=Schino|first1=Gabriele|last2=Pellegrini|first2=Barbara|journal=International Journal of Primatology|volume=32|issue=2|pages=406–414|s2cid=2899244|url-access=subscription}}</ref> During grooming, subordinates prefer to pick at other mandrills from behind, in order to minimize eye contact and give them more time to flee if the more dominant individual attacks. The recipients of grooming will try to maneuver the groomer to pick at more "risky" areas.<ref>{{cite journal|author1=Schino, G.|author2=De Angelis, F.|year=2020|title=Conflict over grooming topography between mandrill groomers and groomees|journal=Behavioural Processes|volume=180| | Both male and female mandrills rub and mark trees and branches with secretions from their chest glands, though males (and especially dominant males) mark more than females. The chemicals in the secretions signal the individual's sex, age and rank. Scent-marking may also serve a [[Territory (animal)|territorial]] function, captive alpha males will mark enclosure boundaries.<ref>{{cite journal|author1=Vaglio, S.|author2=Minicozzi, P.|author3=Romoli, R.|display-authors=etal|year=2016|title=Sternal gland scent-marking signals sex, age, rank, and group identity in captive mandrills|journal=Chemical Senses|volume=41|issue=2|pages=177–186|doi=10.1093/chemse/bjv077|pmid=26708734|doi-access=free|hdl=2436/601458|hdl-access=free}}</ref> Mandrills will [[Social grooming|groom]] one another, even when there is no benefit to be gained from doing so.<ref>{{Cite journal|url=https://link.springer.com/article/10.1007/s10764-010-9477-4|doi=10.1007/s10764-010-9477-4|title=Grooming and the expectation of reciprocation in mandrills (''Mandrillus sphinx'')|year=2011|last1=Schino|first1=Gabriele|last2=Pellegrini|first2=Barbara|journal=International Journal of Primatology|volume=32|issue=2|pages=406–414|s2cid=2899244|url-access=subscription}}</ref> During grooming, subordinates prefer to pick at other mandrills from behind, in order to minimize eye contact and give them more time to flee if the more dominant individual attacks. The recipients of grooming will try to maneuver the groomer to pick at more "risky" areas.<ref>{{cite journal|author1=Schino, G.|author2=De Angelis, F.|year=2020|title=Conflict over grooming topography between mandrill groomers and groomees|journal=Behavioural Processes|volume=180|article-number=104240|doi=10.1016/j.beproc.2020.104240|pmid=32905823|s2cid=221501684}}</ref> | ||
===Reproduction and development=== | ===Reproduction and development=== | ||
[[File:Male Mandrill.jpg|thumb|left|"Fatted" male mandrill showing colorful posterior|alt=Adult male mandrill showing a red, blue and purple rump]] | [[File:Male Mandrill.jpg|thumb|left|"Fatted" male mandrill showing colorful posterior|alt=Adult male mandrill showing a red, blue and purple rump]] | ||
[[Dominance hierarchy|Dominant]] or alpha male mandrills have the most mating success. Upon gaining alpha status, males develop larger testicles, redder faces and posteriors, more secretion from the chest glands and fatter sides and rumps. When a male loses dominance, these physiological changes are at least partially reversed.<ref name="Setchell 2001" >{{cite journal|author1=Setchell, J. M.|author2=Dixson, A. F.|title=Changes in the secondary sexual adornments of male mandrills (''Mandrillus sphinx'') are associated with gain and loss of alpha status|pmid=11300708|year=2001|volume=39|issue=3|pages=177–184|doi=10.1006/hbeh.2000.1628|journal=Hormones and Behavior|s2cid=7560147}}</ref> The blue facial skin is more consistent in brightness.<ref name="Setchell 2001" /><ref name="Setchell 2002">{{cite journal|author1=Setchell, J. M.|author2=Dixson, A. F.|title=Developmental variables and dominance rank in adolescent male mandrills (''Mandrillus sphinx'')|pmid=11793410|year=2002|volume=56|issue=1|pages=9–25|doi=10.1002/ajp.1060|journal=American Journal of Primatology|s2cid=25762754}}</ref> Higher ranking males tend to have more contrast between red and blue facial coloring.<ref name="Renoult 2011"/> Due to their distribution of fat, dominant males are also known as "fatted" males while subordinate males are known as "non-fatted" males.{{sfn|Dixson|2015|pp=18, 120}} Canine length also correlates with dominance, and males are less likely to sire offspring when their canines are under {{convert|30|mm|abbr=on}}.<ref name="Leigh 2008"/> In some individuals, the development of [[secondary sexual characteristic]]s is [[Neoteny|suppressed]] in response to competition from other males.<ref name=arresteddevelopment>{{cite journal|author1=Setchell, J. M.|author2=Dixson, A. F.|year=2001|title=Arrested development of secondary sexual adornments in subordinate adult male mandrills (''Mandrillus sphinx'')|journal=American Journal of Physical Anthropology|volume=115|issue=3|pages=245–252|doi=10.1002/ajpa.1079|pmid=11424076}}</ref> Male mandrills tend to establish dominance with vocalizations and facial expressions, rather than fighting.<ref name="Setchell 2005">{{cite journal|author1=Setchell, J. M.|author2=Wickings, E. J.|year=2005|title=Dominance, status signals and coloration in male mandrills (''Mandrillus sphinx'')|journal=Ethology|volume=111|issue=1|pages=25–50|doi=10.1111/j.1439-0310.2004.01054.x|bibcode=2005Ethol.111...25S }}</ref> | [[Dominance hierarchy|Dominant]] or alpha male mandrills have the most mating success. Upon gaining alpha status, males develop larger testicles, redder faces and posteriors, more secretion from the chest glands and fatter sides and rumps. When a male loses dominance, these physiological changes are at least partially reversed.<ref name="Setchell 2001" >{{cite journal|author1=Setchell, J. M.|author2=Dixson, A. F.|title=Changes in the secondary sexual adornments of male mandrills (''Mandrillus sphinx'') are associated with gain and loss of alpha status|pmid=11300708|year=2001|volume=39|issue=3|pages=177–184|doi=10.1006/hbeh.2000.1628|journal=Hormones and Behavior|s2cid=7560147}}</ref> The blue facial skin is more consistent in brightness.<ref name="Setchell 2001" /><ref name="Setchell 2002">{{cite journal|author1=Setchell, J. M.|author2=Dixson, A. F.|title=Developmental variables and dominance rank in adolescent male mandrills (''Mandrillus sphinx'')|pmid=11793410|year=2002|volume=56|issue=1|pages=9–25|doi=10.1002/ajp.1060|journal=American Journal of Primatology|s2cid=25762754 |url=https://durham-repository.worktribe.com/output/1541325 }}</ref> Higher ranking males tend to have more contrast between red and blue facial coloring.<ref name="Renoult 2011"/> Due to their distribution of fat, dominant males are also known as "fatted" males while subordinate males are known as "non-fatted" males.{{sfn|Dixson|2015|pp=18, 120}} Canine length also correlates with dominance, and males are less likely to sire offspring when their canines are under {{convert|30|mm|abbr=on}}.<ref name="Leigh 2008"/> In some individuals, the development of [[secondary sexual characteristic]]s is [[Neoteny|suppressed]] in response to competition from other males.<ref name=arresteddevelopment>{{cite journal|author1=Setchell, J. M.|author2=Dixson, A. F.|year=2001|title=Arrested development of secondary sexual adornments in subordinate adult male mandrills (''Mandrillus sphinx'')|journal=American Journal of Physical Anthropology|volume=115|issue=3|pages=245–252|doi=10.1002/ajpa.1079|pmid=11424076 |bibcode=2001AJPA..115..245S |url=https://durham-repository.worktribe.com/output/1565051 }}</ref> Male mandrills tend to establish dominance with vocalizations and facial expressions, rather than fighting.<ref name="Setchell 2005">{{cite journal|author1=Setchell, J. M.|author2=Wickings, E. J.|year=2005|title=Dominance, status signals and coloration in male mandrills (''Mandrillus sphinx'')|journal=Ethology|volume=111|issue=1|pages=25–50|doi=10.1111/j.1439-0310.2004.01054.x|bibcode=2005Ethol.111...25S }}</ref> | ||
Mating occurs mostly during the dry season, with female [[ovulation]] peaking between June and September. Receptive females have [[sexual swelling]]s on their posteriors,{{sfn|Dixson|2015|pp=61, 77}} and the red facial coloration can communicate age and fertility.<ref>{{cite journal|author1=Setchell, J. W.|author2=Wickings, E. J.|author3=Knapp, L. A.|year=2006|title=Signal content of red facial coloration in female mandrills (''Mandrillus sphinx'')|journal=Proceedings of the Royal Society B: Biological Sciences|volume=273|issue=1500|pages=2395–2400|doi=10.1098/rspb.2006.3573|pmid=16928644|pmc=1636084}}</ref> Males also appear to detect a female's reproductive state using the [[vomeronasal organ]] (known as the [[flehmen response]]).<ref>{{cite journal|author1=Charpentier, M. J. E.|author2=Mboumba, S.|author3=Ditsoga, C.|author4=Drea, C. M.|year=2013|title=Nasopalatine ducts and flehmen behavior in the mandrill: reevaluating olfactory communication in Old World primates|journal=American Journal of Primatology|volume=75|issue=1|pages=703–714|doi=10.1002/ajp.22146|pmid=23526642|s2cid=25612927}}</ref> Dominant males try to monopolize access to females by mate guarding, which involves the male tending to and [[Copulation (zoology)|copulating]] with a female for days.{{sfn|Dixson|2015|p=91}} Dominant males tend to sire most of the offspring, but they are less able to monopolize access to the females when many females reach [[estrus]] at the same time. A subordinate male is also more likely to have reproductive success if he is closely related to an alpha male.<ref name="Charpentier 2005">{{cite journal|author=Charpentier, M.|author2=Peignot, P.|author3=Hossaert-McKey, M.|author4=Gimenez, O.|author5=Setchell, J. M.|author6=Wickings, E. J.|title=Constraints on control: factors influencing reproductive success in male mandrills (Mandrillus sphinx)|doi=10.1093/beheco/ari034|year=2005|journal=Behavioral Ecology|volume=16|issue=3|pages=614–623|doi-access=free}}</ref> An ovulating female tends to allow the brightest colored males to come near her and touch her [[perineum]], and is more likely to groom and solicit them.<ref>{{cite journal|author=Setchell, J. M.|year=2005|title=Do female mandrills prefer brightly colored males?|journal=International Journal of Primatology|volume=26|issue=4|pages=715–735|doi=10.1007/s10764-005-5305-7|s2cid=3082991|url=http://dro.dur.ac.uk/12176/1/12176.pdf}}</ref> The female signals her willingness to mate by positioning her posterior towards the male. Intercourse lasts no more than 60 seconds, with the male mounting the female and making pelvic thrusts.{{sfn|Dixson|2015|pp=61–62}} | Mating occurs mostly during the dry season, with female [[ovulation]] peaking between June and September. Receptive females have [[sexual swelling]]s on their posteriors,{{sfn|Dixson|2015|pp=61, 77}} and the red facial coloration can communicate age and fertility.<ref>{{cite journal|author1=Setchell, J. W.|author2=Wickings, E. J.|author3=Knapp, L. A.|year=2006|title=Signal content of red facial coloration in female mandrills (''Mandrillus sphinx'')|journal=Proceedings of the Royal Society B: Biological Sciences|volume=273|issue=1500|pages=2395–2400|doi=10.1098/rspb.2006.3573|pmid=16928644|pmc=1636084}}</ref> Males also appear to detect a female's reproductive state using the [[vomeronasal organ]] (known as the [[flehmen response]]).<ref>{{cite journal|author1=Charpentier, M. J. E.|author2=Mboumba, S.|author3=Ditsoga, C.|author4=Drea, C. M.|year=2013|title=Nasopalatine ducts and flehmen behavior in the mandrill: reevaluating olfactory communication in Old World primates|journal=American Journal of Primatology|volume=75|issue=1|pages=703–714|doi=10.1002/ajp.22146|pmid=23526642|s2cid=25612927}}</ref> Dominant males try to monopolize access to females by mate guarding, which involves the male tending to and [[Copulation (zoology)|copulating]] with a female for days.{{sfn|Dixson|2015|p=91}} Dominant males tend to sire most of the offspring, but they are less able to monopolize access to the females when many females reach [[estrus]] at the same time. A subordinate male is also more likely to have reproductive success if he is closely related to an alpha male.<ref name="Charpentier 2005">{{cite journal|author=Charpentier, M.|author2=Peignot, P.|author3=Hossaert-McKey, M.|author4=Gimenez, O.|author5=Setchell, J. M.|author6=Wickings, E. J.|title=Constraints on control: factors influencing reproductive success in male mandrills (Mandrillus sphinx)|doi=10.1093/beheco/ari034|year=2005|journal=Behavioral Ecology|volume=16|issue=3|pages=614–623|doi-access=free}}</ref> An ovulating female tends to allow the brightest colored males to come near her and touch her [[perineum]], and is more likely to groom and solicit them.<ref>{{cite journal|author=Setchell, J. M.|year=2005|title=Do female mandrills prefer brightly colored males?|journal=International Journal of Primatology|volume=26|issue=4|pages=715–735|doi=10.1007/s10764-005-5305-7|s2cid=3082991|url=http://dro.dur.ac.uk/12176/1/12176.pdf}}</ref> The female signals her willingness to mate by positioning her posterior towards the male. Intercourse lasts no more than 60 seconds, with the male mounting the female and making pelvic thrusts.{{sfn|Dixson|2015|pp=61–62}} | ||
| Line 134: | Line 134: | ||
[[File:JaxZoo 11-23-16-6061.jpg|thumb|Mandrill infant perched on mother|alt=Mandrill infant grabbing onto mother's back]] | [[File:JaxZoo 11-23-16-6061.jpg|thumb|Mandrill infant perched on mother|alt=Mandrill infant grabbing onto mother's back]] | ||
Mandrill gestation lasts an average of 175 days with most births taking place between January and March, during the wet season. Gaps in between births range from 184 to 1,159 days with an average of 405 days.<ref name="Setchell2002">{{Cite journal|last1=Setchell|first1=J. M.|last2=Lee|first2=P. C.|last3=Wickings|first3=E. J.|last4=Dixson|first4=A. F.|title=Reproductive parameters and maternal investment in mandrills (''Mandrillus sphinx'')|journal=International Journal of Primatology|volume=23|pages=51–68|year=2002|doi=10.1023/A:1013245707228|s2cid=25158600}}</ref> and tend to be shorter in higher ranking females.{{sfn|Dixson|2015|p=112}} Infants are born at an average weight of {{convert|640|g|abbr=on}}, and mostly bare-skinned with some white hair and a tuft of dark hair on the head and along the spine. Over the next two or three months, they develop their adult hair color on the body, limbs and head while the flesh-colored face and snout darken.{{sfn|Dixson|2015|p=19}} Dependent infants are carried on their mothers' bellies.{{sfn|Dixson|2015|p=36}}<ref name="Abernethy 2002"/> Young are typically weaned at around 230 days old. Males become more sexually dimorphic between four and eight years old, at which point females are already beginning to give birth.<ref name=Ontogeny/> Males start leaving their horde after they reach six years old.<ref name="Abernethy 2002"/> Females reach their adult size around seven years while males do so at ten years.<ref name=Ontogeny>{{cite journal|author1=Setchell, J. M.|author2=Lee, P. C.|author3=Wickings, E. J.|author4=Dixson, A. F.|year=2001|title=Growth and ontogeny of sexual size dimorphism in the mandrill (''Mandrillus sphinx'')|journal=American Journal of Physical Anthropology|volume=115|issue=4|pages=349–360|doi=10.1002/ajpa.1091|pmid=11471133}}</ref> | Mandrill gestation lasts an average of 175 days with most births taking place between January and March, during the wet season. Gaps in between births range from 184 to 1,159 days with an average of 405 days.<ref name="Setchell2002">{{Cite journal|last1=Setchell|first1=J. M.|last2=Lee|first2=P. C.|last3=Wickings|first3=E. J.|last4=Dixson|first4=A. F.|title=Reproductive parameters and maternal investment in mandrills (''Mandrillus sphinx'')|journal=International Journal of Primatology|volume=23|pages=51–68|year=2002|doi=10.1023/A:1013245707228|s2cid=25158600}}</ref> and tend to be shorter in higher ranking females.{{sfn|Dixson|2015|p=112}} Infants are born at an average weight of {{convert|640|g|abbr=on}}, and mostly bare-skinned with some white hair and a tuft of dark hair on the head and along the spine. Over the next two or three months, they develop their adult hair color on the body, limbs and head while the flesh-colored face and snout darken.{{sfn|Dixson|2015|p=19}} Dependent infants are carried on their mothers' bellies.{{sfn|Dixson|2015|p=36}}<ref name="Abernethy 2002"/> Young are typically weaned at around 230 days old. Males become more sexually dimorphic between four and eight years old, at which point females are already beginning to give birth.<ref name=Ontogeny/> Males start leaving their horde after they reach six years old.<ref name="Abernethy 2002"/> Females reach their adult size around seven years while males do so at ten years.<ref name=Ontogeny>{{cite journal|author1=Setchell, J. M.|author2=Lee, P. C.|author3=Wickings, E. J.|author4=Dixson, A. F.|year=2001|title=Growth and ontogeny of sexual size dimorphism in the mandrill (''Mandrillus sphinx'')|journal=American Journal of Physical Anthropology|volume=115|issue=4|pages=349–360|doi=10.1002/ajpa.1091|pmid=11471133 |bibcode=2001AJPA..115..349S }}</ref> | ||
===Communication=== | ===Communication=== | ||
[[File:Meaningful-Gesture-in-Monkeys?-Investigating-whether-Mandrills-Create-Social-Culture-pone.0014610.s007.ogv|thumb|right|Female mandrill facepalming|alt=Video of captive female mandrill shuffling though hay and facepalming]] | [[File:Meaningful-Gesture-in-Monkeys?-Investigating-whether-Mandrills-Create-Social-Culture-pone.0014610.s007.ogv|thumb|right|Female mandrill facepalming|alt=Video of captive female mandrill shuffling though hay and facepalming]] | ||
Mandrills communicate with various facial expressions and postures. Threat displays involve open mouth staring, usually in combination with head bobbing, ground slapping and [[Hackles|raised hair]]. These gestures are usually performed by dominant individuals towards subordinates, who respond with bared teeth grimaces, signaling fear and aggression. Both young and low-ranking females show submission and anxiety with a pouting "duck face". Playful intentions are communicated with a relaxed open-mouth face. Males approaching females display a "grin" or silent bared-teeth face and make lip-smacks. This display may also occur with teeth-chattering.{{sfn|Dixson|2015|pp=50–55}} Mandrills can develop and pass on new gestures; captive individuals at the [[Colchester Zoo]], England [[facepalm]] to discourage being disturbed, particularly while resting.<ref>{{cite journal|author=Laidre, M. E.|year=2011|title=Meaningful gesture in monkeys? Investigating whether mandrills create social culture|journal=PLOS ONE|volume=6|issue=2| | Mandrills communicate with various facial expressions and postures. Threat displays involve open mouth staring, usually in combination with head bobbing, ground slapping and [[Hackles|raised hair]]. These gestures are usually performed by dominant individuals towards subordinates, who respond with bared teeth grimaces, signaling fear and aggression. Both young and low-ranking females show submission and anxiety with a pouting "duck face". Playful intentions are communicated with a relaxed open-mouth face. Males approaching females display a "grin" or silent bared-teeth face and make lip-smacks. This display may also occur with teeth-chattering.{{sfn|Dixson|2015|pp=50–55}} Mandrills can develop and pass on new gestures; captive individuals at the [[Colchester Zoo]], England [[facepalm]] to discourage being disturbed, particularly while resting.<ref>{{cite journal|author=Laidre, M. E.|year=2011|title=Meaningful gesture in monkeys? Investigating whether mandrills create social culture|journal=PLOS ONE|volume=6|issue=2|article-number=e14610|doi=10.1371/journal.pone.0014610|pmid=21311591|pmc=3032724|bibcode=2011PLoSO...614610L|doi-access=free}}</ref> | ||
Mandrills also produce several vocalizations, for both long and short distances. During group movements, adult males produce two-phase grunts and one-syllable roars, both of which are equivalent to the "wahoo" bark of baboons. Other group members produce "crowings", which last almost two seconds and start as a vibration and transition into a longer harmonic sound. Short distance vocals include the "yak", a sharp, repeating, pulse-like call produced by all individuals except for adult males and made in tense situations. Mandrills may also grunt during aggressive encounters. Growls are used to express mild alarm while intense alarms come in the form of a short, two-syllable sharp call known as the "k-alarm". A sharp, loud "K-sound" is produced for unknown reasons. Screaming is a signal of fear and made by individuals fleeing, while the [[girneys|girney]], a type of moan or purr, is made as a form of appeasement or frustration among females and young.<ref>{{cite journal|author=Kudo, H.|title=The study of vocal communication of wild mandrills in Cameroon in relation to their social structure|doi=10.1007/BF02381013|year=1987|journal=Primates|volume=28|issue=3|pages=289–308|s2cid=1507136}}</ref>{{sfn|Dixson|2015|p=47}} Individual voices are more similar among related animals, but unrelated mandrills can have similar voices if they regularly interact.<ref>{{cite journal|author1=Levréro, F.|author2=Carrete-Vega, G.|author3=Herbert, A.|display-authors=etal|year=2015|title=Social shaping of voices does not impair phenotype matching of kinship in mandrills|journal=Nature Communications|volume=6| | Mandrills also produce several vocalizations, for both long and short distances. During group movements, adult males produce two-phase grunts and one-syllable roars, both of which are equivalent to the "wahoo" bark of baboons. Other group members produce "crowings", which last almost two seconds and start as a vibration and transition into a longer harmonic sound. Short distance vocals include the "yak", a sharp, repeating, pulse-like call produced by all individuals except for adult males and made in tense situations. Mandrills may also grunt during aggressive encounters. Growls are used to express mild alarm while intense alarms come in the form of a short, two-syllable sharp call known as the "k-alarm". A sharp, loud "K-sound" is produced for unknown reasons. Screaming is a signal of fear and made by individuals fleeing, while the [[girneys|girney]], a type of moan or purr, is made as a form of appeasement or frustration among females and young.<ref>{{cite journal|author=Kudo, H.|title=The study of vocal communication of wild mandrills in Cameroon in relation to their social structure|doi=10.1007/BF02381013|year=1987|journal=Primates|volume=28|issue=3|pages=289–308|s2cid=1507136}}</ref>{{sfn|Dixson|2015|p=47}} Individual voices are more similar among related animals, but unrelated mandrills can have similar voices if they regularly interact.<ref>{{cite journal|author1=Levréro, F.|author2=Carrete-Vega, G.|author3=Herbert, A.|display-authors=etal|year=2015|title=Social shaping of voices does not impair phenotype matching of kinship in mandrills|journal=Nature Communications|volume=6|article-number=7609|doi=10.1038/ncomms8609|pmid=26139329|bibcode=2015NatCo...6.7609L|doi-access=free}}</ref> | ||
==Threats and conservation== | ==Threats and conservation== | ||
| Line 153: | Line 153: | ||
===Works cited=== | ===Works cited=== | ||
* {{cite book|last=Dixson|first=Alan F.|year=2015|title=The Mandrill: A Case of Extreme Sexual Selection|publisher=Cambridge University Press|isbn=978-1-107-11461-6}} | * {{cite book|last=Dixson|first=Alan F.|year=2015|title=The Mandrill: A Case of Extreme Sexual Selection|publisher=Cambridge University Press|isbn=978-1-107-11461-6}} | ||
{{C.Cercopithecinae nav}} | {{C.Cercopithecinae nav}} | ||
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[[Category:Mandrillus]] | [[Category:Mandrillus]] | ||
[[Category:Primates of Africa]] | [[Category:Primates of Africa]] | ||
[[Category: | [[Category:Animal taxa named by Carl Linnaeus]] | ||
[[Category:Tool-using mammals]] | [[Category:Tool-using mammals]] | ||
[[Category:Vulnerable animals]] | [[Category:Vulnerable animals]] | ||
[[Category:Vulnerable biota of Africa]] | [[Category:Vulnerable biota of Africa]] | ||
Latest revision as of 01:53, 19 December 2025
Template:Short description Script error: No such module "about". Script error: No such module "Distinguish". Template:Top icon Template:Use dmy dates Template:Use American English Template:Speciesbox
The mandrill (Mandrillus sphinx) is a large Old World monkey native to west central Africa. It is one of the most colorful mammals in the world, with red and blue skin on its face and posterior. The species is sexually dimorphic, as males have a larger body, longer canine teeth and brighter coloring. Its closest living relative is the drill, with which it shares the genus Mandrillus. Both species were traditionally thought to be baboons, but further evidence has shown that they are more closely related to white-eyelid mangabeys.
Mandrills mainly live in tropical rainforests but will also travel across savannas. They are active during the day and spend most of their time on the ground. Their preferred foods are fruit and seeds, but mandrills will consume leaves, piths, mushrooms, and animals from insects to juvenile bay duiker. Mandrills live in large, stable groups known as "hordes" which can number in the hundreds. Females form the core of these groups, while adult males are solitary and only reunite with the larger groups during the breeding season. Dominant males have the most vibrant colors and fattest flanks and rumps, and have the most success siring young.
The mandrill is classified as vulnerable on the IUCN Red List. Its biggest threats are habitat destruction and hunting for bushmeat. Gabon is considered the stronghold for the species. Its habitat has declined in Cameroon and Equatorial Guinea, while its range in the Republic of the Congo is limited.
Etymology
The word mandrill is derived from the English words man and drill—the latter meaning Template:Gloss or Template:Gloss and being West African in origin—and dated to 1744.[1][2][3] The name appears to have originally referred to chimpanzees.[4] The first scholar to record the name for the colorful monkey was Georges-Louis Buffon in 1766. It was called the "tufted ape", "great baboon" and "ribbernosed baboon" by Thomas Pennant in A Synopsis of Quadrupeds (1771) and A History of Quadrupeds (1781).Template:Sfn
Taxonomy
The mandrill was first scientifically depicted in Historia animalium (1551–1558) by Conrad Gessner, who considered it a kind of hyena.Template:Sfn The species was formally classified by Carl Linnaeus as Simia sphinx in 1758. Its current generic name Mandrillus was coined by Ferdinand Ritgen in 1824.[5]
Historically, some scientists placed the mandrill and the closely related drill (M. leucophaeus) in the baboon genus Papio. Morphological and genetic studies in the late 20th and early 21st centuries found a closer relationship to white-eyelid mangabeys of the genus Cercocebus. Some have even proposed that the mandrill and drill belong to Cercocebus.Template:Sfn Two genetic studies in 2011 clarified Mandrillus and Cercocebus as separate sister lineages.[6][7] The two genera split around 4.5 million years ago (mya) while the mandrill and drill split approximately 3.17 mya. Fossils of Mandrillus have not been found.Template:Sfn
Some authorities have divided mandrill populations into subspecies: the northern mandrill (M. s. sphinx) and the southern mandrill (M. s. madarogaster). A proposed third subspecies, M. s. insularis, was based on the mistaken belief that mandrills are present on Bioko Island.Template:Sfn[8] The consensus is that mandrills belong to one subspecies (M. s. sphinx).Template:Sfn
Cytochrome-b sequences suggest that mandrill populations north and south of the Ogooué River split 800,000 years ago and belong to distinct haplogroups. This divergence appears to have also led to the splitting of the mandrill strain of the simian immunodeficiency virus (SIV).[9] The draft (incomplete) genome of the mandrill was published in 2020, with a reported genome size of 2.90 giga–base-pairs and high levels of heterozygosity.[10]
Characteristics
The mandrill has a stocky body with a large head and muzzle, as well as a short and stumpy tail.Template:Sfn The limbs are evenly sized and the fingers and toes are more elongated than those in baboons,[11] with a more opposable big toe on the feet.Template:Sfn The mandrill is the most sexually dimorphic primate,[12] and it is the largest monkey.Template:Sfn Females are less stocky and have shorter, flatter snouts.Template:Sfn Males have a Template:Cvt head-body length and weigh Template:Cvt while females have a Template:Cvt head-body length and weigh Template:Cvt.[13] Most of the teeth are larger in males,[14] and the canine teeth reach up to Template:Cvt and Template:Cvt long for males and females respectively.[12] Both sexes have Template:Cvt long tails.[13]
The coat of the mandrill is primarily grizzled or banded olive-brown with a yellow-orange beard and sparse, light hairs on its underside.Template:Sfn[13] The lips are surrounded by stiff white whiskers, and white bare skin exists behind the ears. Male mandrills have a "crest" of long hairs on the head and neck, while both sexes have chest glands which are covered by long hairs. The face, rump and genitals have less hair.Template:Sfn The mandrill has a red line running down the middle of their face which connects to their red nose. On either side of the line, the skin is blue and grooved.[13]Template:Sfn In males, the blue skin is supported by ridged bone swellings. Females have more subdued facial coloring, but this can vary between individuals with some having stronger red and blue hues and others being darker or almost black.Template:Sfn In males, the rump and areas around the genitals are multi-colored, consisting of red, pink, blue and purple skin,[11]Template:Sfn with a red penis shaft and violet scrotum. The genital and anal areas of the female are red.Template:Sfn
The mandrill is among the most colorful mammals. Charles Darwin wrote in The Descent of Man: "no other member of the whole class of mammals is coloured in so extraordinary a manner as the adult male mandrill".[15] The red coloration is created by blood vessels near the surface of the skin,[16] while the blue is a form of structural coloration caused by parallel arrangements of collagen fibers.[17] The blue ridges on males contrast with both the red facial hues and the green foliage of their environment, helping them stand out to other individuals.[18] The darker and more subdued coloring of female faces is caused by melanin.Template:Sfn
Ecology
The mandrill lives in west-central Africa, including southern Cameroon, mainland Equatorial Guinea (Río Muni), Gabon and parts of the Republic of the Congo. Its range is bounded by the Sanaga River to the north and the Ogooué and Ivindo Rivers to the east. It does not appear to share habitat with the drill, as the two species are separated by the Sanaga River.Template:Sfn Mandrills live in tropical rainforests, generally preferring primary forests over secondary forests. They also live in patchy gallery forests surrounded by savanna and travel across grass areas within their forest habitats.[19] They have also been recorded in mountainous areas, near rivers and in cultivated fields.[20]
Mandrills prefer thick bush dominated by perennial plants like gingers and plants of the genera Brillantaisia and Phaulopsis.[13][20] They mainly dwell on the ground, but feed as high as the canopy.[19] Both mandrills and drills are more arboreal than baboons.[11] Mandrills may aggregate or compete with other primates such as talapoins, guenons, mangabeys, black-and-white colobuses, chimpanzees, and gorillas.[19][20]
Diet
The mandrill is an omnivore. The core of its diet consists of plants, of which it eats over a hundred species.[21] In Lopé National Park, the mandrill's diet was composed of fruit (50.7%), seeds (26.0%), leaves (8.2%), pith (6.8%), flowers (2.7%), and animal matter (4.1%), with other foods making up the remaining 1.4%.[22] During the wet season, mandrills forage in continuous forest, when fruit is most available, while during the dry season they feed in gallery forests and at the borders of savannas and forests.[23] The mandrill's preferred fruits include those of the cashew species Pseudospondias microcarpa, the coffee species Nauclea diderrichii and the wort species Psorospermum febrifugum.[23] Mandrills consume more seeds than many other primate species.[21] Adult male mandrills are one of the few primates capable of biting through the hard shell of Detarium microcarpum seeds.[22] For vegetation, they mostly eat the young leaves, shoots and piths of monocot plants.[21] In particular, mandrills consume leaves from the arrowroots Haumania liebrechtsiana and Trachyphrynium braunianum, as well as the piths of ginger plants like Renealmia macrocolia and species in the genus Aframomum.[23] They are also known to consume mushrooms.[21]
The rest of a mandrill's diet is largely made up of invertebrates, particularly ants, termites, crickets, spiders, snails, and scorpions. They also eat birds and their eggs, frogs and rodents.[21][24] Mandrills have been recorded preying on larger vertebrates such as juvenile bay duikers. Such prey is killed with a bite to the head followed by pulling off the hind limbs and tearing open the belly. Individuals may cooperate during hunting and share kills.[24]
Predators, parasites and pathogens
Leopards may prey on mandrills, as traces of mandrill have been found in their feces.[25] Other potential predators include African rock pythons, crowned eagles and chimpanzees.[19]Template:Sfn Leopards are a threat to all individuals, while eagles are only threats to the young.[26]Template:Sfn In a study where a mandrill group was exposed to models of leopards and crown eagles, the leopard models tended to cause the mandrills to flee up trees while the eagles were more likely to drive them to take cover. The dominant male did not flee from either model types; in the case of the leopards, he paced around while looking in their direction. Alarm calls were more commonly heard in response to leopards than eagles.[26]
Mandrills can become infected with gastrointestinal parasites, such as nematodes and protozoa. Tumbu fly larvae may live under the skin and individuals that walk through grassland can get infested with ticks. Blood parasites include the malaria-causing Plasmodium and the nematode Loa loa, which is transmitted by bites from deer flies.Template:Sfn Wild mandrills have tested positive for SIV, enteroviruses of the species EV-J and astroviruses, including a human variant.[9][27]
Behavior and life history
Mandrills are mostly diurnal and are awake around 10 hours per day from morning to dusk.[21][28] They often pick a new tree to sleep in every night.[21] Mandrills have been observed using tools; in captivity, they use sticks to clean themselves.[29] In the wild, mandrills appear to live 12–14 years, but captive individuals can live 30–40 years.Template:Sfn
Social structure
Mandrills live in large "supergroups" or "hordes" that can contain hundreds of individuals.[23]Template:Sfn[30] These large groups are fairly stable and do not appear to be gatherings of smaller ones. At Lopé National Park, Gabon, mandrill hordes were found to have an average of 620 individuals, and some groups were as large as 845, making them possibly the largest cohesive groups of wild primates.[30] Another study in Lopé found that a horde of 625 mandrills consisted of 21 dominant males, 71 less dominant and subadult males, 247 adult and adolescent females, 200 juveniles, and 86 dependent infants.[23] A mandrill horde of around 700 individuals in northern Lopé had a total home range of Script error: No such module "convert"., Script error: No such module "convert". of which was suitable habitat. The supergroup would occasionally diverge into two to four subgroups before reuniting.[31] Another 15-month long study of a 120-member group found a home range of Script error: No such module "convert". with an average traveling distance of Script error: No such module "convert". per day.[28]
Hordes consist of matrilineal family groups, and females are important for maintaining social cohesion. Strong connections with their relatives may lead to support during conflicts, higher survival rate of offspring and a longer lifespan for females. Dominant females are at the center of the group network and their removal leads to fewer social connections in the group.[32] The social rank of a mother mandrill can contribute to the social rank of both her female and male offspring.[33] Mature males are not permanent members of hordes but join as females become sexually receptive and leave as their sexual cycle ends. As a result, the coloration of the male mandrill may be intended to attract attention in a social structure with no long-term relationships between mates.[30] Higher ranking males are found in the center of a social group while lower ranking males are more likely to occupy the periphery.[34] Females have some control over the males and coalitions can expel an unwanted male from a group.[35] Outside the breeding season, males are believed to lead a solitary life and all-male bachelor groups are not known to exist.[30]
Both male and female mandrills rub and mark trees and branches with secretions from their chest glands, though males (and especially dominant males) mark more than females. The chemicals in the secretions signal the individual's sex, age and rank. Scent-marking may also serve a territorial function, captive alpha males will mark enclosure boundaries.[36] Mandrills will groom one another, even when there is no benefit to be gained from doing so.[37] During grooming, subordinates prefer to pick at other mandrills from behind, in order to minimize eye contact and give them more time to flee if the more dominant individual attacks. The recipients of grooming will try to maneuver the groomer to pick at more "risky" areas.[38]
Reproduction and development
Dominant or alpha male mandrills have the most mating success. Upon gaining alpha status, males develop larger testicles, redder faces and posteriors, more secretion from the chest glands and fatter sides and rumps. When a male loses dominance, these physiological changes are at least partially reversed.[16] The blue facial skin is more consistent in brightness.[16][39] Higher ranking males tend to have more contrast between red and blue facial coloring.[18] Due to their distribution of fat, dominant males are also known as "fatted" males while subordinate males are known as "non-fatted" males.Template:Sfn Canine length also correlates with dominance, and males are less likely to sire offspring when their canines are under Script error: No such module "convert"..[12] In some individuals, the development of secondary sexual characteristics is suppressed in response to competition from other males.[34] Male mandrills tend to establish dominance with vocalizations and facial expressions, rather than fighting.[40]
Mating occurs mostly during the dry season, with female ovulation peaking between June and September. Receptive females have sexual swellings on their posteriors,Template:Sfn and the red facial coloration can communicate age and fertility.[41] Males also appear to detect a female's reproductive state using the vomeronasal organ (known as the flehmen response).[42] Dominant males try to monopolize access to females by mate guarding, which involves the male tending to and copulating with a female for days.Template:Sfn Dominant males tend to sire most of the offspring, but they are less able to monopolize access to the females when many females reach estrus at the same time. A subordinate male is also more likely to have reproductive success if he is closely related to an alpha male.[43] An ovulating female tends to allow the brightest colored males to come near her and touch her perineum, and is more likely to groom and solicit them.[44] The female signals her willingness to mate by positioning her posterior towards the male. Intercourse lasts no more than 60 seconds, with the male mounting the female and making pelvic thrusts.Template:Sfn
Mandrill gestation lasts an average of 175 days with most births taking place between January and March, during the wet season. Gaps in between births range from 184 to 1,159 days with an average of 405 days.[45] and tend to be shorter in higher ranking females.Template:Sfn Infants are born at an average weight of Script error: No such module "convert"., and mostly bare-skinned with some white hair and a tuft of dark hair on the head and along the spine. Over the next two or three months, they develop their adult hair color on the body, limbs and head while the flesh-colored face and snout darken.Template:Sfn Dependent infants are carried on their mothers' bellies.Template:Sfn[30] Young are typically weaned at around 230 days old. Males become more sexually dimorphic between four and eight years old, at which point females are already beginning to give birth.[33] Males start leaving their horde after they reach six years old.[30] Females reach their adult size around seven years while males do so at ten years.[33]
Communication
Mandrills communicate with various facial expressions and postures. Threat displays involve open mouth staring, usually in combination with head bobbing, ground slapping and raised hair. These gestures are usually performed by dominant individuals towards subordinates, who respond with bared teeth grimaces, signaling fear and aggression. Both young and low-ranking females show submission and anxiety with a pouting "duck face". Playful intentions are communicated with a relaxed open-mouth face. Males approaching females display a "grin" or silent bared-teeth face and make lip-smacks. This display may also occur with teeth-chattering.Template:Sfn Mandrills can develop and pass on new gestures; captive individuals at the Colchester Zoo, England facepalm to discourage being disturbed, particularly while resting.[46]
Mandrills also produce several vocalizations, for both long and short distances. During group movements, adult males produce two-phase grunts and one-syllable roars, both of which are equivalent to the "wahoo" bark of baboons. Other group members produce "crowings", which last almost two seconds and start as a vibration and transition into a longer harmonic sound. Short distance vocals include the "yak", a sharp, repeating, pulse-like call produced by all individuals except for adult males and made in tense situations. Mandrills may also grunt during aggressive encounters. Growls are used to express mild alarm while intense alarms come in the form of a short, two-syllable sharp call known as the "k-alarm". A sharp, loud "K-sound" is produced for unknown reasons. Screaming is a signal of fear and made by individuals fleeing, while the girney, a type of moan or purr, is made as a form of appeasement or frustration among females and young.[47]Template:Sfn Individual voices are more similar among related animals, but unrelated mandrills can have similar voices if they regularly interact.[48]
Threats and conservation
As of 2019, the IUCN Red List lists the mandrill as vulnerable. Its total population is unknown but is suspected to have decreased by more than 30 percent over the last 24 years. Its main threats are habitat destruction and hunting for bushmeat.[49] The mandrill appears to have suffered massive habitat loss in Equatorial Guinea and southern Cameroon, while its range in the Republic of the Congo is limited and its status is unknown.Template:Sfn In addition, while mandrills live in groups numbering in the hundreds, hunting in Cameroon and Equatorial Guinea appears to have led to smaller group sizes.[49] Gabon is seen as the most important remaining refuge for the species, and the country's low population density and vast rainforests make it a good candidate for mandrill conservation. Surveys have shown high population numbers for other primate species like chimpanzees and gorillas. A semi-wild population exists at the International Centre of Medical Research of Franceville.Template:Sfn
The mandrill is listed under Appendix I by CITES, banning commercial trade in wild-caught specimens, and under Class B by the African Convention, which provides them protection but allows special authorization for their killing, capturing or collecting.[49][50][51] There is at least one protected area for mandrills within each of the countries they inhabit.[49] In Gabon, most of the rainforests have been leased to timber companies but around 10 percent is part of a national parks system, 13 of which were established in 2002.Template:Sfn
References
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Works cited
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Script error: No such module "Navbox". Template:Taxonbar Template:Authority control
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- Fauna of Central Africa
- Mammals described in 1758
- Mammals of Cameroon
- Mammals of Equatorial Guinea
- Mammals of Gabon
- Mammals of the Republic of the Congo
- Mandrillus
- Primates of Africa
- Animal taxa named by Carl Linnaeus
- Tool-using mammals
- Vulnerable animals
- Vulnerable biota of Africa