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Temporal range: 39.75–0 Ma
Late Eocene - Recent
Various canid species: Arctic fox (top left), Red fox (top right), Grey wolf (bottom left) and coyote (bottom right)
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Suborder: Caniformia
Family: Canidae
G. Fischer de Waldheim, 1817
Genera and species

See text

Canidae (11px /ˈkænɨd/) [2] is the biological family of carnivorous and omnivorous mammals that includes domestic dogs, wolves, foxes, jackals, coyotes, and many other lesser known extant and extinct dog-like mammals. A member of this family is called a canid (/ˈknɨd/). The Canidae family is divided into two tribes: Canini (related to wolves) and Vulpini (related to foxes). The two species of the basal Caninae are more primitive and do not fit into either tribe.


Classification and relationship

The subdivision of Canidae into "foxes" and "true dogs" may not be in accordance with the actual relations; also the taxonomic classification of several canines is disputed. Recent DNA analysis shows that Canini (dogs) and Vulpini (foxes) are valid clades. (See phylogeny below). Molecular data implies a North American origin of living Canidae and an African origin of wolf-like canines (Canis, Cuon, and Lycaon).[3]

Currently, the domestic dog is listed as a subspecies of Canis lupus, C. l. familiaris, and the dingo (also considered a domestic dog) as C. l. dingo, provisionally a separate subspecies from C. l. familiaris; the red wolf, eastern Canadian wolf, and Indian wolf are recognized as subspecies.[1] Many sources list the domestic dog as Canis familiaris, but others, including the Smithsonian Institution and the American Society of Mammalogists, more precisely list it as a subspecies of C. l. familiaris; the red wolf, eastern Canadian wolf, and Indian wolf may or may not be separate species; the dingo has been in the past variously classified as Canis dingo, Canis familiaris dingo and Canis lupus familiaris dingo.


Evolution of the Canids
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An approximate timescale of key events in canid evolution.
For precise dates, see text.
Axis scale: millions of years ago.

Eocene epoch

Carnivorans evolved from miacoids about 55 million years ago during the late Paleocene.[4] Then, about 50 million years ago, the carnivorans split into two main divisions: caniforms (dog-like) and feliforms (cat-like). By 40 million years ago the first clearly identifiable member of the dog family Canidae had arisen. It was called Prohesperocyon wilsoni and was found in what is now southwestern Texas. This fossil species bears a combination of features that definitively mark it as a canid: teeth that include the loss of the upper third molar (a general trend toward a more shearing bite), and the characteristically enlarged bony bulla (the rounded covering over the middle ear). Based on what we know about its descendants, Prohesperocyon likely had slightly more elongated limbs than its predecessors, along with toes that were parallel and closely touching, rather than splayed, as in bears.[5]

The Canidae family soon subdivided into three subfamilies, each of which diverged during the Eocene: Hesperocyoninae (~39.74-15 Mya), Borophaginae (~34-2 Mya), and the Caninae (~34-0 Mya) lineage that led to present-day canids (wolves, foxes, coyotes, jackals, and domestic dogs). Each of these groups showed an increase in body mass with time, and sometimes exhibited a specialised hypercarnivorous diet that made them prone to extinction.[6]:Fig. 1 Only the Caninae lineage, commonly referred to as "canines", survived to the present day.

Oligocene epoch

By the Oligocene, all three subfamilies of canids (Hesperocyoninae, Borophaginae, and Caninae) had appeared in the fossil records of North America. The earliest and most primitive branch of the Canidae was the Hesperocyoninae lineage, which included the coyote-sized Mesocyon of the Oligocene (38-24 Mya). These early canids probably evolved for fast pursuit of prey in a grassland habitat, and resembled modern civets in appearance. Hesperocyonines eventually became extinct in the middle Miocene. One of the early member of the Hesperocyonines, the genus Hesperocyon, gave rise to Archaeocyon and Leptocyon. These branches led to the borophagine and canine radiations.[7]

Miocene epoch

Around 9-10 Mya during the Late Miocene, Canis, Urocyon, and Vulpes genera expanded from southwestern North America. This was the point where the canine radiation began. The success of these canines was related to the development of lower carnassials that were capable of both mastication and shearing. Around 8 Mya, Beringia offered the canines a way to enter Eurasia.

Pliocene epoch

During the Pliocene around (4-5 Mya) Canis lepophagus appeared in North America. This was small and sometimes coyote-like. Others were wolf-like in characteristics. It is theorized that Canis latrans (the coyote) descended from Canis lepophagus.[8]

The formation of the Isthmus of Panama about 3 Mya joined South America to North America, allowing canids to invade the former, where they diversified.

Pleistocene epoch

Around 1.5 to 1.8 Mya, a variety of wolves were present in Europe. Also, the North American wolf line appeared with Canis edwardii, clearly identifiable as a wolf. Canis rufus appeared, possibly a direct descendent of Canis edwardii. Around 0.8 Mya, Canis ambrusteri emerged in North America. A large wolf, it was found all over the continent. It is thought that this species migrated to South America where it became the ancestor of Canis dirus, the dire wolf.

At 0.3 Mya Canis lupus (the gray wolf) was fully developed and had spread throughout Europe and northern Asia. Beringia offered a way to North America.[9] At around 100,000 years ago, the dire wolf, one of the largest members of the dog family, had spread from South America to southern Canada and from coast to coast. The dire wolf shared its habitat with the gray wolf. Around 8,000 years ago the dire wolf became extinct.


Wild canids are found on every continent except Antarctica, and inhabit a wide range of different habitats, including deserts, mountains, forests, and grassland. They vary in size from the fennec fox at 24 cm (9.4 in) long, to the gray wolf, which may be up to 2 m (6.6 ft) long, and can weigh up to 80 kg (180 lb).

With the exceptions of the bush dog, raccoon dog and some domestic breeds, canids have relatively long legs and lithe bodies, adapted for chasing prey. All canids are digitigrade, meaning that they walk on their toes. They possess bushy tails, non-retractile claws, and, excepting the African wild dog (Lycaon pictus), a dewclaw on the front feet. They possess a baculum, which together with a cavernous body helps to create a copulatory tie during mating, locking the animals together for up to an hour. Young canids are born blind, with their eyes opening a few weeks after birth.[10] All living canids (Caninae) have a ligament analogous to the nuchal ligament of ungulates used to maintain the posture of the head and neck with little active muscle exertion; this ligament allows them to conserve energy while running long distances following scent trails with their nose to the ground.[11] However, at least some Borophaginae (such as Aelurodon) are believed to lack this ligament based upon skeletal details of the neck.[11]

Only a few species are arboreal - the North American gray fox, the closely related Channel Island fox,[12] and the raccoon dog habitually climb trees.[13][14][15]

Social behavior

Almost all canids are social animals and live together in groups. In most foxes and in many of the true dogs, a male and female pair work together to hunt and to raise their young. Gray wolves and some of the other larger canids live in larger groups called packs. African wild dogs have the largest packs, which can number as many as 90 animals. Some species form packs or live in small family groups depending on the circumstances, including the type of available food. In most species, there are also some individuals who live on their own. Within a canid pack, there is a system of dominance so that the strongest, most experienced animals lead the pack. In most cases, the dominant male and female are the only pack members to breed.

Canids communicate with each other by scent signals, by visual clues and gestures, and by vocalizations such as growls, barks, and howls. In most cases, groups have a home territory from which they drive out others. The territory is marked by leaving urine scent marks, which warn trespassing individuals.[16]

Most canids bear young once a year, from 1 to 16 or more (in the case of the African wild dog) at a time. The young are born small and helpless and require a long period of care. They are kept in a den, most often dug into the ground, for warmth and protection. When they begin eating solid food, both parents, and often other pack members, bring food back for them from the hunt. This is most often vomited up from the adult's stomach. Young canids may take a year to mature and learn the skills they need to survive.[17]


Most canids have 42 teeth, with a dental formula of: Unknown extension tag "math". As in other members of Carnivora, the upper fourth premolar and lower first molar are adapted as carnassial teeth for slicing flesh. The molar teeth are strong in most species, allowing the animals to crack open bone to reach the marrow. The deciduous or baby teeth formula in canids is 3 1 3; molars are completely absent.

Species and taxonomy


Subfamily Caninae

File:Canidae Species Divesity.png
Fluctuation of species within Canidae over 40 million years

Prehistoric Canidae

Classification of Hesperocyoninae from Wang (1994)[18] and Borophaginae from Wang, Tedford, Taylor (1999),[19] and Caninae from Tedford, Wang, Taylor (2009)[20] except where noted.



(Ma = million years ago) (million years = in existence)


(Ma = million years ago)

    • Genus Cynodesmus (32-29 Ma)
      • Cynodesmus martini (29 Ma)
      • Cynodesmus thooides (32 Ma)
    • ?Genus Caedocyon
      • Caedocyon tedfordi
    • Genus Ectopocynus (32-19 Ma)
      • Ectopocynus antiquus (32 Ma)
      • Ectopocynus intermedius (29 Ma)
      • Ectopocynus siplicidens (19 Ma)
    • Genus Enhydrocyon (29-25 Ma)
      • Enhydrocyon basilatus (25 Ma)
      • Enhydrocyon crassidens (25 Ma)
      • Enhydrocyon pahinsintewkpa (29 Ma)
      • Enhydrocyon stenocephalus (29 Ma)
    • Genus Hesperocyon (39.74-34 Ma)
      • Hesperocyon coloradensis
      • Hesperocyon gregarius (37 Ma)
    • Genus Mesocyon (34-29 Ma)
      • Mesocyon brachyops (29 Ma)
      • Mesocyon coryphaeus (29 Ma)
      • Mesocyn temnodon
    • Genus Osbornodon (32-18 Ma)
      • Osbornodon brachypus
      • Osbornodon fricki (18 Ma)
      • Osbornodon iamonensis (21 Ma)
      • Osbornodon renjiei (33 Ma)
      • Osbornodon scitulus[23]
      • Osbornodon sesnoni (32 Ma)
      • Osbornodon wangi[21]
    • Genus Paraenhydrocyon (30-25 Ma)
    • Genus Philotrox (29 Ma)
      • Philotrox condoni (29 Ma)
    • Genus Prohesperocyon (36 Ma)
      • Prohesperocyon wilsoni (36 Ma)
    • Genus Sunkahetanka (29 Ma)
      • Sunkahetanka geringensis (29 Ma)

Canids and humans

One canid, the domestic dog, a subspecies of the gray wolf, long ago entered into a partnership with humans and today remains one of the most widely kept domestic animals in the world and serves humanity in a great many important ways.

Among canids, only the gray wolf has been known to prey on humans.[24] There are at least two records of coyotes killing humans,[25] and two of golden jackals killing children.[26] Some canid species have also been trapped and hunted for their fur and, especially the gray wolf and the red fox, for sport. Some canids are now endangered in the wild due to hunting, habitat loss, and the introduction of diseases from domestic dogs.[27]

See also


  1. 1.0 1.1 Script error
  2. Canidae. Dictionary.com. The American Heritage Stedman's Medical Dictionary. Houghton Mifflin Company. http://dictionary.reference.com/browse/Canidae (accessed: February 16, 2009).
  3. Lindblad-toh, K.; Wade, CM; Mikkelsen, TS; Karlsson, EK; Jaffe, DB; Kamal, M; Clamp, M; Chang, JL et al. (2005). "Genome sequence, comparative analysis and haplotype structure of the domestic dog" (PDF). Nature 438 (7069): 803–819. PMID 16341006. doi:10.1038/nature04338. Retrieved 2008-04-27. 
  4. "The Paleobiology Database". Paleodb.org. Retrieved 2012-06-12. 
  5. Wang, Xiaoming (2008). "How Dogs Came to Run the World". Natural History Magazine. July/August. Retrieved 2008-11-28. 
  6. Van Valkenburgh, B.; Wang, X.; Damuth, J. (Oct 2004). "Cope's Rule, Hypercarnivory, and Extinction in North American Canids". Science 306 (5693): 101–104. Bibcode:2004Sci...306..101V. ISSN 0036-8075. PMID 15459388. doi:10.1126/science.1102417.  More than one of |author2= and |last2= specified (help); More than one of |author3= and |last3= specified (help) edit
  7. Martin, L.D. 1989. Fossil history of the terrestrial carnivora. Pages 536 - 568 in J.L. Gittleman, editor. Carnivore Behavior, Ecology, and Evolution, Vol. 1. Comstock Publishing Associates: Ithaca.
  8. Nowak, R.M. 1979. North American Quaternary Canis. Monograph of the Museum of Natural History, University of Kansas 6:1 - 154.
  9. Nowak, R. 1992. Wolves: The great travelers of evolution. International Wolf 2(4):3 - 7.
  10. Macdonald, D. (1984). The Encyclopedia of Mammals. New York: Facts on File. p. 57. ISBN 0-87196-871-1. 
  11. 11.0 11.1 Wang, Xiaoming and Tedford, Richard H. Dogs: Their Fossil Relatives and Evolutionary History. New York: Columbia University Press, 2008. pp.97-8
  12. "ADW: Urocyon littoralis: INFORMATION". Animaldiversity.ummz.umich.edu. 1999-11-28. Retrieved 2012-06-12. 
  13. Kauhala K. & Saeki M. (2004). »Raccoon Dog«. Canid Species Accounts. IUCN/SSC Canid Specialist Group. Pridobljeno 15.4.2009.
  14. Ikeda, Hiroshi (August 1986). "Old dogs, new tricks: Asia's raccoon dog, a venerable member of the canid family is pushing into new frontiers". Natural History 95 (8): p40,44. 
  15. Raccoon dog – Nyctereutes procyonoides. WAZA – World Association of Zoos and Aquariums.
  16. Nowak, R. M., and J. L. Paradiso. 1983. Walker's Mammals of the World. Baltimore, Maryland: The Johns Hopkins University Press. ISBN 0-8018-2525-3.
  17. Voelker, W. 1986. The Natural History of Living Mammals. Medford, New Jersey: Plexus Publishing. ISBN 0-937548-08-1
  18. Wang, Xiaoming (1994). "Phylogenetic systematics of the Hesperocyoninae". Bulletin of the American Museum of Natural History 221: 1–207. hdl:2246/829. 
  19. Wang, Xiaoming (1999). "Phylogenetic systematics of the Borophaginae". Bulletin of the American Museum of Natural History 243: 1–391. hdl:2246/1588. 
  20. 20.0 20.1 Tedford, Richard; Xiaoming Wang, Beryl E. Taylor (2009). "Phylogenetic systematics of the North American fossil Caninae (Carnivora: Canidae)". Bulletin of the American Museum of Natural History 325: 1–218. doi:10.1206/574.1. 
  21. 21.0 21.1 Hayes, F.G. (2000). "The Brooksville 2 local fauna (Arikareean, latest Oligocene) Hernando County, Florida". Bulletin of the Florida Museum of Natural History 43 (1): 1–47. 
  22. Wang, Xiaoming; Wideman, Benjamin C.; Nichols, Ralph; Hanneman, Debra L. (2004). "A new species of Aelurodon (Carnivora, Canidae) from the Barstovian of Montana" (PDF). Journal of Vertebrate Paleontology 24 (2): 445–452. doi:10.1671/2493. Archived from the original on September 30, 2007. Retrieved 2007-07-08. 
  23. Wang, Xiaoming (2003). "New Material of Osbornodon from the Early Hemingfordian of Nebraska and Florida" (PDF). Bulletin of the American Museum of Natural History 279: 163–176. doi:10.1206/0003-0090(2003)279<0163:C>2.0.CO;2. 
  24. Kruuk, H. 2002. Hunter and Hunted: Relationships between Carnivores and People. Cambridge, UK: Cambridge University Press. ISBN 0-521-81410-3.
  25. "Coyote Attacks: An Increasing Suburban Problem". Archived from the original on February 24, 2006. Retrieved 2007-08-19. 
  26. "Canis aureus". Animal Diversity Web. Retrieved 2007-07-31. 
  27. ICUN Red List

General references

  • Xiaoming Wang, Richard H. Tedford, Mauricio Antón, Dogs: Their Fossil Relatives and Evolutionary History, New York : Columbia University Press, 2008; ISBN 978-0-231-13528-3

External links