Primate

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Primates[1]
Fossil range: Late Cretaceous - Recent
Olive Baboon, an Old World monkey
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Infraclass: Eutheria
Superorder: Euarchontoglires
Order: Primates
Linnaeus, 1758
Range of the non-human primates
Range of the non-human primates
Families

A primate is any member of the biological order Primates, the group that contains all the species commonly related to the lemurs, monkeys, and apes, with the last category including humans.[2] Primates are found all over the world. Non-human primates occur mostly in Central and South America, Africa, and South Asia. A few species exist as far north in the Americas as southern Mexico, and as far north in Asia as northern Japan.

The order Primates was established by Carl Linnaeus in 1758, in the tenth edition of his book Systema Naturae,[3] for the genera Homo (humans), Simia (other apes and monkeys), Lemur (prosimians) and Vespertilio (bats). In the first edition of the same book (1735), he had used the name Anthropomorpha for Homo, Simia and Bradypus (sloths).[4] In 1839, Henri-Marie Ducrotay de Blainville, following Linnaeus and imitating his nomenclature, established the orders Secundates (including the suborders Chiroptera, Insectivora and Carnivora), Tertiates (or Glires) and Quaternates (including Gravigrada, Pachydermata and Ruminantia),[5] but these new taxa were not accepted.

The Latin primas means "one of the first, excellent, noble" (nominative plural primates). The English singular primate was derived via back-formation from the Latin inflected form.[6]

The Primates order is divided informally into three main groupings: prosimians, monkeys of the New World, and monkeys and apes of the Old World. The prosimians are species whose bodies most closely resemble that of the early proto-primates. The most well known of the prosimians, the lemurs, are located on the island of Madagascar and to a lesser extent on the Comoros Islands, isolated from the rest of the world. The New World monkeys include the familiar capuchin, howler, and squirrel monkeys. They live exclusively in the Americas. Discounting humans, the rest of the simians, the Old World monkeys and the apes, inhabit Africa and southern and central Asia, although fossil evidence shows many species existed in Europe as well.

According to fossil evidence, primitive ancestors of primates already existed in the late Cretaceous. Molecular clock studies suggest that the primate branch is even more ancient (originating at least in the mid-Cretaceous). They are now thought to be most closely related to flying lemurs and, more distantly, to treeshrews. They probably have descended from Plesiadapiformes.

Contents

[edit] Description and behaviour

Homo sapiens, a member of the order Primates
Homo sapiens, a member of the order Primates

[edit] General description

Primates have radiated in arboreal habitats and therefore retain many characteristics are adaptations to this environment. They can be either herbivorous or omnivorous. They have a primitive (unspecialized) body plan, 2 mammary glands, 1-2 young per pregnancy and a long gestation and developmental period. Primates are frequently highly social, with flexible dominance hierarchies.[7] New World species form monogamous pair bonds, and show substantial paternal care of young unlike most Old World monkeys.

[edit] Skull


[edit] Eyes

Primates have forward-facing colour binocular vision which was useful for the brachiating ancestors of humans, particularly for finding and collecting food, although recent studies suggest it was more useful in courtship.[citation needed] Strepsirrhines have a postorbital bar, a bone which runs around the eyesocket, to protect their eyes, which is in contrast to the higher primates, haplorrhines, which have evolved fully enclosed sockets.[8]

[edit] Hands and feet

All primates have five digits on each limb (pentadactyly), with keratin nails on the anterior ends. The ventral sides of the hands and feet have tactile pads on the distal phalanges. They have opposable thumbs, which are a characteristic primate feature, but are not limited to this order; opossums, for example, also have opposing thumbs. These thumbs allow some species to use tools to perform some tasks. In primates, the combination of opposing thumbs, short fingernails (rather than claws) and long, inward-closing fingers is a relic of the ancestral practice of gripping branches, and has, in part, allowed some species to develop brachiation as a significant means of transportation. Prosimians have clawlike nails on the second toes of their feet.

[edit] Limbs and vertebral column

The primate clavicle is retained as prominent element of the pectoral girdle, this allows the shoulder joint broad mobility. Apes have more mobile shoulder joints and arms due to the dorsal position of the scapula, broad ribcages that are flatter front-to-back, and a shorter, less mobile spine compared to Old World monkeys (with caudal vertebrae greatly reduced, resulting in tail loss in some species).

[edit] Prehensile tail

Old World monkeys are unlike apes in that most have tails, and unlike the New World monkeys in that their tails are never prehensile. Only the New World Atelidae family have prehensile tails.

[edit] Mouth and teeth

Primates have a shortened rostrum (snout).[7] Prosimians are distinguished by their immobilized upper lips, moist tip to their nose and forward-facing lower front teeth. Primates have a considerably varied dental pattern. Some primates have lost most of their incisors, although all retain at least one lower incisor. In most strepsirhines, the lower incisors form a toothcomb which is thought to be used in grooming and possibly foraging. Old World monkeys also have eight premolars, compared with twelve in New World monkeys. The Old World species are divided into apes and monkeys depending on the number of cusps on their molars (apes have five—the "Y-5" molar pattern, Old World monkeys have only four in a bilophodont pattern). A hypocone evolved in early primate history, while the paraconid was lost, leaving both upper and lower teeth with a basically quadrate pattern. Primitively, primate molars were brachydont and tuberculosectorial, but they have become bunodont and quadrate in a number of modern forms.[9]

[edit] Nose

Technically, the distinction of Old World monkeys from New World monkeys depends on the structure of the nose, and the distinction of Old World monkeys from apes depends on dentition. In New World monkeys the nostrils face sideways, whilst in Old World monkeys, they face downwards.

[edit] Sexual dimorphism

Simians show some degree of sexual dimorphism. Old World species (apes and some monkeys) often exhibit sexual dimorphism, which can also be found to a lesser degree in some New World species. Recent studies have mainly used the technique of comparative analysis to examine both the variation in the expression of the dimorphism among primates and the fundamental causes of sexual dimorphism. Primates usually have dimorphism in body mass[10][11] and canine tooth size[12][13] along with pelage and skin colour.[14] The dimorphism in primates has been attributed to many factors:

  • Mating system - Polygynous species are more sexually dimorphic than monogamous species, such as the New World monkeys.[15] It is also associated with greater male gonadal investment than what is found in closely related monogamous species.[16][17]
  • Size - Larger species are more sexually dimorphic than smaller species.[15]
  • Habitat - Terrestrial species tend to be more sexually dimorphic than arboreal species. It is possible that male-male competition in terrestrial species is more dependent on body size.
  • Diet - Frugivores, for reasons that are not clear, are slightly more sexually dimorphic than folivores.[17] Energy may be less of a constraint, or maybe females may be more clumped around an area of fruit trees.

Comparative analyses have substantiated the sexual selection hypotheses, and have generated a more complete understanding of the relationship between sexual selection, natural selection, and mating systems in primates. Studies are helping to find the relative contribution of the various selective and non-selective mechanisms in sexual dimorphism evolution and expression.[18] These studies have shown that dimorphism is the product of changes in both male and female traits. Ontogenic scaling, where relative extension of a common growth trajectory occurs, may show some insight into the relationship between sexual dimorphism and growth patterns.[19] There is some evidence from the fossil record that suggests that there was convergent evolution of dimorphism, and some extinct hominids probably exceeded dimorphism of any living primate.

[edit] Color vision

Color vision in primates is unique in the evolution of most eutherian mammals. While our remote vertebrate ancestors possessed trichromacy, our nocturnal, warm-blooded, mammalian ancestors lost one of three cones in the retina at the time of dinosaurs. Fish, reptiles and birds are therefore trichromatic while all mammals, with the exception of some primates and marsupials,[20] are strictly dichromats.

Primates achieve trichromacy through color receptors (cone cells), with spectral peaks in the violet (short wave, S), green (middle wave, M), and yellow-green (long wave, L) wavelengths. All primates, however, are not capable of trichromacy. The catarrhines are routinely trichromatic, meaning that both males and females possess three opsins (pigments) sensitive to 430 nm, 530 nm, and 560 nm wavelengths.[21] Platyrrhines, on the other hand are non-routinely trichromatic; only a small population of platyrrhines are trichromats.[22]

Howler monkeys have reinvented routine trichromatism through a recent gene duplication of the red-green opsin gene.[23] This has allowed trichromacy for both sexes, the X chromosome has gained two loci to house both the green allele and the red allele. Howler monkeys are perhaps the most folivorous of the New World monkeys. Fruits are not part of their diet, and the type of leaves they consume (young, nutritive, and digestible), are detectable only by a red-green signal. Field work exploring the dietary preferences of howler monkeys suggest that routine trichromacy was environmentally selected for.[22]

[edit] Locomotion

Various species of primates move by brachiation, bipedalism, leaping, arboreal and terrestrial quadrupedalism, climbing or knuckle walking.

Most prosimians are arboreal quadrupedalists and climbers. Many are also terrestrial quadrupedalists, while some are leapers. Most monkeys are both arboreal and terrestrial quadrupedalists and climbers. Gibbons are brachiators. Chimps, orangutans, and gorillas all knuckle walk, and can move bipedally for short distances. Humans are the only fully bipedal species.

[edit] Laughter

Laughter may not be confined or unique to humans, despite Aristotle's observation that "only the human animal laughs". But some behavioural psychologists argue that self-awareness of one's situation, or the ability to identify with somebody else's predicament, are prerequisites for laughter, so animals do not laugh like humans do.

Chimpanzees, gorillas, and orangutans show laughter-like vocalizations in response to physical contact, such as wrestling, play chasing, or tickling. This is documented in wild and captive chimpanzees. Chimpanzee laughter is not readily recognizable to humans as such, because it is generated by alternating inhalations and exhalations that sound more like breathing and panting. The differences between chimpanzee and human laughter may be the result of adaptations that have evolved to enable human speech. There are instances in which non-human primates have been reported to have expressed joy. One study analyzed and recorded sounds made by human babies and Bonobos (a species of chimpanzee) when they were tickled. It found although the Bonobo's laugh was a higher frequency, the laugh followed the same spectrographic pattern of human babies to include as similar facial expressions. Humans and chimpanzees share similar ticklish areas of the body such as the armpits and belly. The enjoyment of tickling in chimpanzees does not diminish with age.[24]

[edit] Habitat

Primates evolved from arboreal animals and many modern species live mostly in trees and hardly ever come to the ground. Other species are partially terrestrial, such as baboons and the Patas Monkey. Only a few species are fully terrestrial, such as the Gelada and Humans. Primates live in a diverse number of forested habitats, including rain forests, mangrove forests, and mountain forests to altitudes of over 3000 m. Although most species are generally shy of water, a few are fine swimmers and are comfortable in swamps and watery areas, including the Proboscis Monkey, De Brazza's Monkey and Allen's Swamp Monkey, which even developed small webbing between its fingers. Some primates, such as the Rhesus Macaque and the Hanuman Langur, can exploit human-modified environments and even live in cities.[citation needed]

[edit] Phylogeny

In older classifications, the Primates were divided into two superfamilies: Prosimii and Anthropoidea. The Prosimii included all of the prosimians: all of Strepsirrhini plus the tarsiers. The Anthropoidea contained all of the simians.

In modern, cladistic reckonings, the Primate order is also a true clade. The suborder Strepsirrhini, the "wet-nosed" primates, split off from the primitive primate line about 63 million years ago (mya). The seven strepsirhine families are the four related lemur families and the three remaining families that include the lorises, the Aye-aye, the galagos, and the pottos.[1] Older classification schemes wrap the Lepilemuridae into the Lemuridae and the Galagidae into the Lorisidae, yielding a three-two family split instead of the four-three split as presented here.[1] Other lineages of lower primates inhabited Earth. During the Eocene, most of the northern continents were dominated by two dominant groups, the adapids and the omomyids. The former is considered a member of Strepsirrhini, but it does not have a tooth-comb like modern lemurs. The latter was related closely to tarsiers, monkeys, and apes. Adapids survived until 10 mya; omomyids on the other hand perished 20 million years earlier.

The Aye-aye is difficult to place in Strepsirrhini.[1] Its family, Daubentoniidae, could be a lemuriform primate and its ancestors split from lemur line more recently than the lemurs and lorises split, about 50 mya. Otherwise it is sister to all of the other strepsirrhines, in which case in evolved away from the main strepsirrhine line between 50 and 63 mya.

The suborder Haplorrhini, the "dry-nosed" primates, is composed of two sister clades.[1] The prosimian tarsiers in family Tarsiidae (monotypic in its own infraorder Tarsiiformes), represent the most primitive division at about 58 mya. The Simiiformes infraorder contains the two parvorders: the New World monkeys in one, and the Old World monkeys, humans and the other apes in the other.[1] This division happened about 40 mya. However about 30 mya, three groups split from the main haplorrhine lineage. One group stayed in Asia and are closest in kin to the "dawn monkey" Eosimias. The second stayed in Africa, where they developed into the Old World primates. The third rafted to South America to become the New World monkeys. Mysteriously the aboriginal Asian Haplorrhini vanished from record once Africa collided with Eurasia 24 mya. Apes and monkeys spread into Europe and Asia. Close behind came lorises and tarsiers, also African castaways. The first hominid fossils were discovered in Northern Africa and date back 7 mya. Modern humans did not appear until 0.2 mya, eventually becoming the most prevalent primate and mammal on Earth.

The discovery of new species happens at a rate of a few new species each year, and the evaluation of current populations as distinct species is in flux. Colin Groves listed about 350 species of primates in Primate Taxonomy in 2001.[25] The recently published third edition of Mammal Species of the World (MSW3) lists 376 species.[1] But even MSW3's list falls short of current understanding as its collection cutoff was in 2003, and a number publications since then have pushed the number of species up to 405. Notable new species not listed in MSW3 include the Bemaraha Woolly Lemur (Avahi cleesei) (named after British actor and lemur enthusiast John Cleese) and the GoldenPalace.com Monkey (whose name was put up for auction).

[edit] Close relations

The Primate order lies in a tight clustering of related orders (the Euarchontoglires) within the Eutheria, a subclass of Mammalia. Recent molecular genetic research on primates, flying lemurs, and treeshrews has shown that the two species of flying lemur (Dermoptera) are more closely related to the primates than the treeshrews of the order Scandentia, even though the treeshrews were at one time considered primates. These three orders make up the Euarchonta clade. This clade combines with the Glires clade (made up of the Rodentia and Lagomorpha) to form the Euarchontoglires clade. Variously, both Euarchonta and Euarchontoglires are ranked as superorders. Also, some scientists consider Dermoptera a suborder of Primates and call the "true" primates the suborder Euprimates (Hoffstetter, 1978) [26] .

Euarchontoglires
Glires

Rodentia (rodents)



Lagomorpha (rabbits, hares, pikas)



Euarchonta

Scandentia (treeshrews)




Dermoptera (flying lemurs)




Plesiadapiformes



Primates







[edit] Classification

Hands and feet of primates
Hands and feet of primates

[edit] Some prehistoric primates

[edit] Primate hybrids

In The Variation Of Animals And Plants Under Domestication Charles Darwin noted: "Several members of the family of Lemurs have produced hybrids in the Zoological Gardens."

Many gibbons are hard to identify based on fur coloration and are identified either by song or genetics. These morphological ambiguities have led to hybrids in zoos. Zoo gibbons usually come from the black market pet trade in Southeast Asia, which transported gibbons across countries all over the region. As a result, perhaps as much as 95% of zoo gibbons are of unknown geographic origin. As most zoos rely on morphological variation or labels that are impossible to verify to assign species and subspecies names, it is unfortunately common for gibbons to be misidentified and housed together. For example, some collections' supposedly pure breeding pairs were actually mixed pairs or hybrids from previous mixed pairs. The hybrid offspring were sent to other gibbon breeders and led to further hybridization in captive gibbons. Within-genus hybrids also occur in wild gibbons where the ranges overlap (Agile Gibbons and Pileated Gibbons x Lar Gibbons, Agile Gibbons x Müller's Bornean Gibbon, Yellow-cheeked Gibbons x Northern White-cheeked Gibbons).

Intergeneric gibbon hybridizations are only known to have occurred in captivity. Silvery Gibbons (Hylobates moloch) and Müller's Bornean Gibbon (H. muelleri) have hybridized with Siamangs (Symphalangus syndactylus) in captivity - a female Siamang produced hybrid "Siabon" offspring on two occasions when housed with a male gibbon; only one hybrid survived.

Anubis Baboons and Hamadryas Baboons have hybridized in the wild where their ranges meet. A Rheboon is a captive-bred Rhesus Macaque/Hamadryas Baboon hybrid with a baboon-like body shape and macaque-like tail.

Different macaque species can interbreed. In "The Variation Of Animals And Plants Under Domestication" Charles Darwin wrote: A Macacus, according to Flourens, bred in Paris; and more than one species of this genus has produced young in London, especially the Macacus rhesus, which everywhere shows a special capacity to breed under confinement. Hybrids have been produced both in Paris and London from this same genus. The Japanese Macaque (Macaca fuscata) has interbred with the introduced Taiwanese Macacque (M. cyclopis) when the latter escaped into the wild from private zoos.

Various hybrid monkeys are bred within the pet trade, for example:

Among Old World monkeys, natural hybridization is not uncommon. There numerous field reports of hybrid monkeys and detailed studies of zones where species overlap and hybrids occur.

Among the great apes, Sumatran and Bornean orangutans are considered separate species with anatomical differences, producing sterile or poorly fertile hybrids. Hybrid orangutans are genetically weaker, with lower survival rates than pure animals.

[edit] Legal status

See also: Non-human primate experiments and International trade in primates
Monkeys, imported for experimentation, in a crate. Credit: BUAV
Monkeys, imported for experimentation, in a crate. Credit: BUAV

Humans are recognized as persons and protected in law by the United Nations Universal Declaration of Human Rights[27] and by all governments, though to varying degrees. Non-human primates are not classified as persons. The status of non-human primates has generated much debate, particularly through the Great Ape Project [28] which argues for the personhood of the non-human members of the family Hominidae. In 1995 Ignaas Spruit, director of Leiden (Netherlands) based Pro-Primates organization, went farther, as he proposed that some rights should be recognized to all non-human primates.[29] In the same way, the American anthropologist Earnest Albert Hooton, enlarging the sense of the famous quote by Terence, used to say "Primas sum: primatum nil a me alienum puto", that is to say: “I am a primate; nothing about primates is outside of my bailiwick”.[30]

[edit] Animal testing

Thousands of primates are used every year around the world in scientific experiments because of their psychological and physiological similarity to humans. Chimpanzees, baboons, marmosets, macaques, and green monkeys are most commonly used in these experiments. In the European Union, around 10,000 were used in 2004, with 4,652 experiments conducted on 3,115 non-human primates in the UK alone in 2005.[31] As of 2004, 3,100 non-human primates were living in captivity in the United States, in zoos, circuses, and laboratories, 1,280 of them being used in experiments.[28] European campaign groups such as the BUAV are seeking a ban on all primate use in experiments as part of the European Union's current review of existing law on animal experimentation.

[edit] See also

[edit] References

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  2. ^ M. Goodman, D. A. Tagle, D. H. Fitch, W. Bailey, J. Czelusniak, B. F. Koop, P. Benson, J. L. Slightom (1990). "Primate evolution at the DNA level and a classification of hominoids". Journal of Molecular Evolution 30: 260–266. doi:10.1007/BF02099995. 
  3. ^ Linnaeus, Carolus (1758). Sistema naturae per regna tria Naturae, secundum classes, ordines, genera, species, cum characteribus differentiis, synonimis locis. Tomus I. Impensis direct. Laurentii Salvii, Holmia, pp. 20-32. 
  4. ^ Linnaeus, Carolus (1735). Sistema naturae sive regna tria Naturae systematice proposita per classes, ordines, genera, & species. apud Theodorum Haak, Lugduni Batavorum, pp. s.p.. 
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  9. ^ Myers, P. (1999). AWD: Primates: Information.
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  11. ^ Lindstedtand & Boyce (1985). "{{{title}}}". Am Nat 125. 
  12. ^ Frisch, J. E. (1963). "Sex-differences in the canines of the gibbon (Hylobates lar)". Primates 4 (2). 
  13. ^ Kay, R. F. (1975). "The functional adaptations of primate molar teeth" 43 (2): 195-215. 
  14. ^ Crook (1972). "Sexual selection, dimorphism, and social organization in the primates", Sexual selection and the descent of man. 
  15. ^ a b Cheverud, J.M., Dow, M. M. & Leutenegger, W. (1985). "The quantitative assessment of phylogenetic constraints in comparative analyses: Sexual dimorphism in body weight among primates". Evolution 39 (6): 1335-1351. 
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  17. ^ a b Leutenegger,W. & Cheverud, J. M. (1982). "Correlates of sexual dimorphism in primates: Ecological and size variables". International Journal of Primatology 3 (4). 
  18. ^ Plavcan, J.M. (2001). "Sexual dimorphism in primate evolution". Am J Phys Anthropol 33: 25-53. 
  19. ^ O'Higgins, P. & Collard, M. (2002). "Sexual dimorphism and facial growth in papionin monkeys". Journal of Zoology 257 (2): 255–272. 
  20. ^ Arrese, C. A., et al (2005). "Cone topography and spectral sensitivity in two potentially trichromatic marsupials, the quokka (Setonix brachyurus) and quenda (Isoodon obesulus)". Proc. Biol. Sci. 272 (1565). doi:10.1098/rspb.2004.3009. 
  21. ^ Bowmaker, J. K., and S. Astell (1991). "Photosensitive and photostable pigments in the retinae of Old World monkeys". J Exp Biol. 156: 1–19. 
  22. ^ a b Surridge, A. K., and D. Osorio (2003). "Evolution and selection of trichromatic vision in primates". Trends in Ecol. and Evol. 18: 198-205. 
  23. ^ Lucas, P. W., and N. J. Dominy (2003). "Evolution and function of routine trichromatic vision in primates". Evolution 57: 2636-2643. 
  24. ^ Johnson, Steven (April 2003). "Emotions and the Brain". Discover 24 (4). 
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  26. ^ McKenna, Malcolm C. and Bell, Susan K. (1997). Classification of Mammals Above the Species Level. Columbia University Press, New York, 329. 
  27. ^ UN Declaration of Human Rights
  28. ^ a b Declaration on Great Apes, Great Ape Project
  29. ^ Spruit, Ignaas (1995). "On Declaring Non-human Primate Rights: An Approach to Primate Protection", in Corbey, Raymond and Theunissen, Bert: Ape, Man, Apeman: Changing Views since 1600. Department of Prehistory, Leiden University, pp. 377-383. 
  30. ^ Hooton, Earnest (1955). "The Importance of Primate Studies in Anthropology", in Gavan, J.A.: The Non-Human Primates and Human Evolution. Wayne University Press, Detroit, pp. 1-10. 
  31. ^ British Union for the Abolition of Vivisection - Primates

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