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Cladus: Eukaryota
Supergroup: Opisthokonta
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Deuterostomia
Phylum: Chordata
Subphylum: Vertebrata
Infraphylum: Gnathostomata
Superclassis: Tetrapoda
Classis: Mammalia
Subclassis: Theria
Infraclassis: Placentalia
Ordo: Carnivora
Subordines: Caniformia - Feliformia - †Miacoidea


Carnivora Bowdich, 1821


* Carnivora on Mammal species of the World.
Mammal Species of the World: A Taxonomic and Geographic Reference, 2 Volume Set edited by Don E. Wilson, DeeAnn M. Reeder

Vernacular names
العربية: آكلات اللحوم
Български: Хищници
Bosanski: Mesožderi
Català: carnivor
Česky: Šelmy
Dansk: Rovdyr
Deutsch: Raubtiere
Ελληνικά: Σαρκοφάγα
English: Carnivores
Español: Carnívoros
Français: Carnivores
עברית: טורפים
Hrvatski: Zvijeri
Magyar: Ragadozók
Italiano: Carnivori
日本語: ネコ目 (食肉目)
한국어: 식육목
Bahasa Melayu: Karnivor
Nederlands: Roofdieren
‪Norsk (bokmål)‬: Rovdyr
Polski: Drapieżne
Русский: Хищные
Slovenščina: Zveri
Suomi: Petoeläimet
Svenska: Rovdjur
Türkçe: Etçiller
Українська: Хижі
Tiếng Việt: (Bộ) Thú ăn thịt
中文: 食肉目


The diverse order Carnivora (pronounced /kɑrˈnɪvərə/ or sometimes /ˌkɑrnɪˈvɔərə/; from Latin carō (stem carn-) "flesh", + vorāre "to devour") includes over 260 species of placental mammals. Its members are formally referred to as carnivorans, while the word "carnivore" (often popularly applied to members of this group) can refer to any meat-eating animal. Carnivorans are the most diverse in size of any mammalian order, ranging from the Least Weasel (Mustela nivalis), at as little as 25 grams (0.88 oz) and 11 centimetres (4.3 in), to the Polar Bear (Ursus maritimus) which can weigh up to 1,000 kilograms (2,200 lb), to the Southern Elephant Seal (Mirounga leonina) whose adult males weigh up to 5,000 kilograms (11,000 lb) and measure up to 6.9 metres (23 ft) in length.

The first carnivoran was a carnivore, and nearly all carnivorans today primarily eat meat. Some, such as cats, pinnipeds, and weasels, are obligate carnivores. Others, such as raccoons and bears, depending on the local habitat, are more omnivorous; the Giant Panda is almost exclusively a herbivore but will take fish, eggs and insects, while the Polar Bear's harsh habitat forces it to mainly subsist on prey. Carnivorans have teeth, claws, and binocular vision adapted for catching and eating other animals. Many hunt in packs and are social animals, giving them an advantage over larger prey.

Carnivorans apparently evolved in North America out of members of the family Miacidae (miacids) c 42 million years ago. They soon split into cat-like and dog-like forms (Feliformia and Caniformia).

Distinguishing features
arnivorans are primarily terrestrial and usually have strong sharp claws, with never fewer than four toes to each foot, and well-developed prominent canine teeth and cheek teeth (premolars and molars) that generally have cutting edges. The last premolar of the upper jaw and first molar of the lower are termed the carnassials or sectorial teeth. These are blade-like teeth that occlude (close) with a scissor-like action for shearing and shredding meat. Carnassials are most highly developed in the Felidae and the least developed in the Ursidae. Carnivorans have six incisors and two conical canines in each jaw. The only two exceptions to this are the Sea Otter (Enhydra lutris), which has four incisors in the lower jaw, and the Sloth Bear (Melursus ursinus), which has four incisors in the upper jaw. The number of molars and premolars is variable between carnivoran species, but all teeth are deeply rooted and are diphyodont. Incisors are retained by carnivorans and the third incisor is commonly large and sharp (canine-like). Carnivorans have either four or five digits on each foot, with the first digit on the forepaws, also known as the dew claw, being vestigial in most species and absent in some.

The Canoidea superfamily (or Caniformia suborder) – Canidae (dogs and foxes), Mephitidae (skunks and stink badgers), Mustelidae (weasels), Procyonidae (raccoons), Ursidae (bears), Otariidae (eared seals), Odobenidae (Walrus), and Phocidae (earless seals) (the last three families formerly classified in the suborder Pinnipedia) and the extinct family Amphicyonidae (bear-dogs) - are characterized by having a non-chambered or partially chambered auditory bullae, non-retractable claws, and well-developed baculum. Most species are rather simply colored, lacking the flashy spotted or rosetted coats like many species of felids and viverrids have. This is because Canoidea tend to range in the temperate and subarctic biomes, although Mustelidae and Procyonidae have a few tropical species. Most are terrestrial, although a few species, like procyonids, are arboreal. All families except the Canidae and a few species of Mustelidae are plantigrade. Diet is varied and most tend to be omnivorous to some degree and thus the carnassial teeth are less specialized. Canoidea have more premolars and molars in an elongated skull.

The Feloidea superfamily (or Feliformia suborder)– Felidae (cats), Herpestidae (mongooses), Hyaenidae (hyenas), Viverridae (civets), and Eupleridae (Malagasy carnivores), as well as the extinct family Nimravidae (paleofelids) – often have spotted, rosetted or striped coats, and tend to be more brilliantly colored than their Canoidean counterparts. This is due to the fact that these species tend to range in tropical habitats, although a few species do inhabit temperate and subarctic habitats. Many are arboreal or semi-arboreal, and the majority are digitigrade. Diet tends to be more strictly carnivorous, especially in the Felidae family. They have fewer teeth and shorter skulls, with much more specialized carnassials meant for shearing meat. Felidae claws are retractile, or rarely, semi-retractile. The terminal phalange with the claw attached folds back in the fore-foot into a sheath by the outer side of the middle phalange of the digit, and is retained in this position when at rest by a strong elastic ligament. In the hind-foot the terminal joint or phalange is retracted on to the top, and not the side of the middle phalange. Deep flexor muscles straighten the terminal phalanges so that the claws protrude from their sheath, and the soft "velvety" paw becomes suddenly converted into a formidable weapon of offence. The habitual retraction of the claws preserves their points from wear.

The Pinnipedia superfamily (walruses, seals, and sea lions), now considered to be part of Caniformia, are medium to large (to 6.5 m) aquatic mammals. Being homeothermic (warm-blooded) marine mammals, pinnipeds need a low surface area to body mass ratio. Otherwise they would suffer from excessive heat loss due to water's high capacity for heat conduction. The body is usually insulated with a thick layer of fat called blubber and typically covered with hair. The digits are not separate, but connected by a thick web that forms flippers for swimming; thus the forelimbs and hindlimbs are transformed into paddles. This enables them to dive at extreme depths (600 meters for the Weddell Seal). They can remain underwater for long periods of time, sometimes over an hour or more, but most dives are usually short. The facial region of skull is relatively small, with pinnae very small or lacking and the vibrissae are well developed. The molariform teeth are mostly homodont and the canines are well developed. The tail is very short or absent, the ears are small or absent as well, and the external genitalia are hidden in slits or depressions in the body.

Skull structure
Members of Carnivora have a characteristic skull shape with relatively large brains encased in a heavy skull. The skull has a highly developed zygomatic arch just behind the maxilla (common to all mammals and their cynodont forebears), and they have ossified external auditory bullae. Feloidea have a two-chambered auditory bullae. In addition to allowing extra room for the passage of muscles to work the lower jaw, the zygomatic arch also allows for differentiation of separate muscle groups to be involved in biting and chewing. Masseters attach from the dentary (specifically, the masseteric fossa) to the zygomatic arch and onto the maxilla in front of the arch, providing crushing force. The temporalis attaches from the dentary (specifically, the coronoid process) to the side of the braincase, providing torque about the axis of jaw articulation. In comparing the skulls of carnivores and herbivores, it can be seen that the shearing force of the temporalis is somewhat more important to carnivores, which have more room on the braincase (this is not unrelated to carnivoran intelligence) and commonly develop a sagittal crest (running from posterior to anterior on the skull) providing yet additional room for temporalis attachment. Carnivoran jaws can only move on a vertical axis, in an up-and-down motion, and cannot move from side-to-side. The jaw joint in carnivores tends to lie within the plane of tooth occlusion; an arrangement that further emphasizes shearing (as in a pair of scissors). In herbivores, the crushing force of the masseters is relatively more important than is shearing. The jaw joint is generally well above the plane of tooth occlusion, allowing extra room for masseteric attachment on the dentary and causing the rotation of the lower jaw to be translated into straight-ahead crushing force between the teeth of the upper and lower jaws.


Carnivora have a simple stomach designed to digest primarily meat, as compared to the elaborate digestive systems of herbivorous animals which are necessary to break down tough, complex plant fibers. The caecum is either absent or short and simple, and the colon is not sacculated or much wider than the small intestine. Most species of Carnivora are, to some degree, omnivorous, except the Felidae and Pinnipedia, which are obligate carnivores. Most have highly-developed senses, especially vision and hearing, and often a highly acute sense of smell in many species, such as in the Canoidea. They are excellent runners: some long-distance runners, but more commonly sprinters. Even bears and raccoons, although seemingly slow and clumsy, are capable of remarkable bursts of speed.

Diet specializations

Carnivorans include carnivores, omnivores, and even a few primarily herbivorous species, such as the Giant Panda. Important teeth for carnivorans are the large, slightly recurved canines, used to dispatch prey, and the carnassial complex, used to rend meat from bone and slice it into digestible pieces. Dogs have molar teeth behind the carnassials for crushing bones, but cats have only a greatly reduced, functionless molar behind the carnassial in the upper jaw. Cats will strip bones clean but will not crush them to get the marrow inside. Omnivores, such as bears and raccoons, have developed blunt, molar-like carnassials. Carnassials are a key adaptation for terrestrial vertebrate predation; all other placental orders are primarily herbivores, insectivores, or aquatic.

Reproductive system
Carnivorans tend to produce a single litter annually, but some produce multiple litters a year, and larger carnivorans like bears have gaps of 2–3 years between litters. The average gestation period lies between 50-115 days, although the ursids and mustelids have delayed implantation, thus extending the gestation period 6–9 months beyond the normal period. Litter sizes are usually small, ranging from 1-13 young, which are born with underdeveloped eyes and ears. In most species, the mother has exclusive or at least primary care of the offspring. Many species of carnivorans are solitary, but a few are gregarious.

Carnivorans evolved out of members of the family Miacidae (miacids). The transition from Miacidae to Carnivora was a general trend in the middle and late Eocene with taxa from both North America and Eurasia involved. The divergence of carnivorans from other miacids, as well as the divergence of the two clades within Carnivora, Caniformia and Feliformia, is now inferred to have happened in the middle Eocene (ca. 42 million years ago). Traditionally the Viverravidae (viverravids) had been thought to be the earliest carnivorans with fossil records first appearing in the Paleocene of North America about 60 million years ago, but recently described evidence from cranial morphology now places them outside the order Carnivora.[1] Traditionally, some paleontologists considered the viverravids to be ancestral to the aeluroid carnivorans (felids, hyaenids, herpestids and viverrids), but this is now doubted.

The Miacidae is not a monophyletic group, but a paraphyletic array of stem taxa. Traditionally, the Miacidae and the Viverravidae had been classified in a third, extinct paraphyletic superfamily, the Miacoidea, from which the direct ancestors of both Carnivora and Creodonta were thought to have arisen. Today Carnivora is restricted to the crown group, and Carnivora and miacoids are grouped together in the clade Carnivoramorpha, and the miacoids are regarded as basal carnivoramorphs. Based on dental features and braincase sizes, it is now known that Carnivora must have evolved from a form even more primitive than Creodonta and thus these two orders may not even be sister groups.[2] The Carnivora, Creodonta, Pholidota, and a few other extinct orders are informally grouped together in the clade Ferae. Older classification schemes divided the order into two suborders: Fissipedia (which included the families of primarily land Carnivora) and Pinnipedia (which included the true seals, eared seals, and Walrus). However, it is now recognized that the Fissipedia is a paraphyletic group and that the pinnipeds were not the sister group to the fissipeds but rather had arisen from among them.

Carnivora are generally divided into the suborders Feliformia (cat-like) and Caniformia (dog-like), the latter of which includes the pinnipeds. The pinnipeds are part of a clade, known as the Arctoidea, which also includes the Ursidae (bears) and the superfamily Musteloidea. The Musteloidea in turn consists of the Mustelidae (mustelids: weasels), Procyonidae (procyonids: raccoons), Mephitidae (skunks) and Ailurus. The oldest caniforms are the Miacis species Miacis cognitus, the Amphicyonidae (Bear-dogs) such as Daphoenus, and Hesperocyon (of the family Canidae, subfamily Hesperocyoninae). Hesperocyonine canids first appeared in North America and the earliest species is currently dated at 39.74 Ma, but they were not represented in Europe until well into the Miocene, and not into Asia and Africa until the Pliocene. Miacis and Amphicyonidae were the first of the caniforms to split from the others and are sometimes considered to be sister groups to Ursidae, but the exact closeness of Amphicyonidae and Ursidae, as well as Arctoidae to Ursidae, is still uncertain. The Canidae (wolves, coyotes, jackals, foxes and dogs) are generally considered to be the sister group to Arctoidea.[2][3][4] The Ursidae first occur in North America in the Late Eocene (ca. 38 million years ago) as the very small and graceful Parictis that had a skull only 7 cm long. Like the canids, this family does not appear in Eurasia and Africa until the Miocene. The other caniform families Amphicyonidae, Mustelidae and Procyonidae occur in both the Old World and the New World by the Late Eocene and Early Oligocene.[2]
The ancestor of all Feliformia evolved from the Caniformia-Feliformia split but the exact position of the Felidae, especially some extinct Felidae, in relation to the other families is somewhat disputed. Nandinia, the African Palm Civet, seems to be the most primitive of all the feliforms and the very first to split from the others. The Asiatic linsangs of the genus Prionodon (traditionally placed in the Viverridae) might form a family of their own as well, as some recent studies indicate that Prionodon is actually the closest living relative to the cats. The Nimravidae are sometimes seen as the most basal of all feliforms and the first to split from the others, but there is a possibility that Nimravidae might not even belong within the order,[4] and therefore its position as a clade within Carnivora is currently unstable. Other studies indicate that Barbourofelids forms a separate family, which is closely related to the true felids instead of being related to the Nimravids. Recognizable Nimravid fossils date from the late Eocene (37 mya), from the Chadronian White River Carnivora Formation at Flagstaff Rim, Wyoming. Nimravid diversity appears to have peaked about 28 mya. The hypercarnivorous (strictly meat-eating) nimravid feliforms were extinct in North America after 26 mya and felids did not arrive in North America until the early middle Miocene (16 mya).

It has been suggested that canids evolved hypercarnivorous morphologies because feliforms were absent during this period (the "cat-gap," 26-18.5 mya), however recent data does not support this hypothesis. Hypercarnivore feliforms (felids and nimravids) occupied an area that canids did not and where felids, nimravids, and hypercarnivorous creodonts are found. Hypercarnivorous canids were present before the disappearance of the nimravids, and all went extinct before the appearance of felids. Following the extinction of nimravids, only three taxa originated, two of which were relatively small in body size. Disparity increased during the "cat-gap" even with the extinction of the hypercarnivorous extremes. This was due to the extinction of morphological intermediates, and because carnivorans began to occupy hypocarnivorous (non-meat-specialist) morphospace for the first time in North America. Procyonids did not arrive in North America until the early Miocene, and "modern" ursids (e.g., Ursinae), did not arrive until the late Miocene. Extinct lineages of Ursidae were present in North America from the late Eocene through the Miocene and Amphicyonid (bear-dogs) were present during this period as well but occupied a morphospace generally shared with canids and not in close proximity to ursids. A large question remains as to why there was a progressive decline in hypercarnivorous carnivoramorphans during the late Oligocene/early Miocene. During this period all hypercarnivorous forms disappeared from the fossil record, including hypercarnivorous feliforms, canids, and mustelids. One possible explanation is climate change. Earth was gradually cooling after the late Paleocene, and over a period spanning the Eocene/Oligocene boundary a dramatic climatic cooling event occurred.[5]

A recent study finally resolves the exact position of Ailurus: the Red Panda is neither a procyonid nor an ursid, but forms a monotypic family with the other musteloids as its closest living relatives. The same study also shows that the mustelids are not a primitive family, as was once thought. Their small body size is a secondary trait — the primitive body form of the arctoids was large, not small.[3] Recent molecular studies also suggest that the endemic Carnivora of Madagascar, including three genera usually classed with the civets and four genera of mongooses classed with the Herpestidae, are all descended from a single ancestor. They form a single sister taxon to the Herpestidae. The hyenas are also closely related to this clade.

1. ^ Polly, David, Gina D. Wesley-Hunt, Ronald E. Heinrich, Graham Davis and Peter Houde (2006). "Earliest Known Carnivoran Auditory Bulla and Support for a Recent Origin of Crown-Clade Carnivora (Eutheria, Mammalia)". Palaeontology 49 (5): 1019–1027. doi:10.1111/j.1475-4983.2006.00586.x.,%202006,%20Viverravus.pdf.
2. ^ a b c Kemp, T.S. (2005). The Origin and Evolution of Mammals. Oxford University Press. ISBN 0198507607.
3. ^ a b Wesley-Hunt, Gina D. and John J. Flynn (2005). "Phylogeny of the Carnivores". Journal of Systematic Palaeontology 3: 1–28. doi:10.1017/S1477201904001518.
4. ^ a b Wesley-Hunt, Gina D. and Lars Werdelin (2005). "Basicranial morphology and phylogenetic position of the upper Eocene carnivoramorphan Quercygale" ([dead link] – Scholar search). Acta Palaeontologica Polonica 50 (4): 837–846.
5. ^ Wesley-Hunt, Gina D. (2005). "The Morphological Diversification of Carnivores in North America". Palaeontology Winter: 35. doi:10.1666/0094-8373(2005)031<0035:TMDOCI>2.0.CO;2.

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