Canis

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Canis
Temporal range: 5.332–0 
Ma
Miocene to present[1]
1st row: wolf (C. lupus),
dog (C. familiaris);
2nd row: red wolf (C. rufus),
eastern wolf (C. lycaon);
3rd row: coyote (C. latrans),
golden jackal (C. aureus);
4th row: Ethiopian wolf (C. simensis),
African wolf (C. lupaster).
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Family: Canidae
Subfamily: Caninae
Tribe: Canini
Subtribe: Canina
Genus: Canis
Linnaeus, 1758[2]
Type species
Canis familiaris
, 1758
Species

Extant:

  • Canis aureus
  • Canis familiaris
  • Canis latrans
  • Canis lupaster
  • Canis lupus
  • Canis lycaon
  • Canis rufus
  • Canis simensis

Extinct:

Canis is a

golden jackals. Species of this genus are distinguished by their moderate to large size, their massive, well-developed skulls and dentition, long legs, and comparatively short ears and tails.[3]

Taxonomy

The

type specimen for genus Canis to the official list.[6]

Canis is primitive relative to Cuon, Lycaon, and Xenocyon in its relatively larger canines and lack of such dental adaptations for hypercarnivory as m1–m2 metaconid and entoconid small or absent; M1–M2 hypocone small; M1–M2 lingual cingulum weak; M2 and m2 small, may be single-rooted; m3 small or absent; and wide palate.

The cladogram below is based on the DNA phylogeny of Lindblad-Toh et al. (2005),[8] modified to incorporate recent findings on Canis species,[9][10]

Canis

Canis latrans (coyote)

Canis rufus (red wolf)

Canis lycaon (Algonquin wolf)

Canis lupus (gray wolf)

Canis familiaris (domestic dog)

African golden wolf)

Canis simensis (Ethiopian wolf)

Canis aureus (golden jackal)

In 2019, a workshop hosted by the

IUCN/SSC Canid Specialist Group recommends that because DNA evidence shows the side-striped jackal (Canis adustus) and black-backed jackal (Canis mesomelas) to form a monophyletic lineage that sits outside of the Canis/Cuon/Lycaon clade, that they should be placed in a distinct genus, Lupulella Hilzheimer, 1906 with the names Lupulella adusta and Lupulella mesomelas.[11]

Evolution

See further: Evolution of the canids

The fossil record shows that

Early Pliocene about 6-5 million YBP the coyote-like Eucyon davisi[13] invaded Eurasia. The canids that had emigrated from North America to Eurasia – Eucyon, Vulpes, and Nyctereutes
– were small to medium-sized predators during the Late Miocene and Early Pliocene but they were not the top predators.

Skulls of dire wolf (Aenocyon dirus), gray wolf (C. lupus), eastern wolf (C. lycaon), red wolf (C. rufus), coyote (C. latrans), African golden wolf (C. lupaster), golden jackal (C. aureus) and black-backed jackal (Lupulella mesomelas)

For Canis populations in the New World, Eucyon in North America gave rise to early North American Canis which first appeared in the Miocene (6 million YBP) in south-western United States and Mexico. By 5 million YBP the larger Canis lepophagus, ancestor of wolves and coyotes, appeared in the same region.[1]: p58 

Around 5 million years ago, some of the Old World Eucyon evolved into the first members of Canis,

C. falconeri.[1]
: p148 

However, a 2021 genetic study of the

Quaternary extinction event, unlike the dire wolf.[14]

Middle Pleistocene and was limited in Eurasia to the small wolves of the Canis mosbachensis–Canis variabilis group and the large hypercarnivorous Canis (Xenocyon) lycaonoides.[16] The hypercarnivore Xenocyon gave rise to the modern dhole and the African wild dog.[1]
: p149 

Dentition and biteforce

Diagram of a wolf skull with key features labelled
Eurasian wolf skull
Bite force adjusted for body weight in Newtons per kilogram[17]
Canid Carnassial Canine
Gray wolf 131.6 127.3
Dhole 130.7 132.0
African wild dog 127.7 131.1
Greenland dog and dingo
117.4 114.3
Coyote 107.2 98.9
Side-striped jackal 93.0 87.5
Golden jackal 89.6 87.7
Black-backed jackal 80.6 78.3

carnassials that are used together in a scissor-like action to shear the muscle and tendon of prey.[1]
: 74 

talonid is used for grinding. The ratio between the trigonid and the talonid indicates a carnivore's dietary habits, with a larger trigonid indicating a hypercarnivore and a larger talonid indicating a more omnivorous diet.[18][19] Because of its low variability, the length of the lower carnassial is used to provide an estimate of a carnivore's body size.[18]

A study of the estimated bite force at the canine teeth of a large sample of living and fossil mammalian predators, when adjusted for their body mass, found that for

canids by the four hypercarnivores that often prey on animals larger than themselves: the African hunting dog (142), the gray wolf (136), the dhole (112), and the dingo (108). The bite force at the carnassials showed a similar trend to the canines. A predator's largest prey size is strongly influenced by its biomechanical limits.[20]

Behavior

Description and sexual dimorphism

Male coyote
Female coyote
Male gray wolf
Female gray wolf

There is little variance among male and female canids. Canids tend to live as monogamous pairs. Wolves,

jackals live in groups that include breeding pairs and their offspring. Wolves may live in extended family groups. To take prey larger than themselves, the African wild dog, the dhole, and the gray wolf depend on their jaws as they cannot use their forelimbs to grapple with prey. They work together as a pack consisting of an alpha pair and their offspring from the current and previous years.[21] Social mammal predators prey on herbivores with a body mass similar to that of the combined mass of the predator pack.[22][23] The gray wolf specializes in preying on the vulnerable individuals of large prey,[24] and a pack of timber wolves can bring down a 500 kg (1,100 lb) moose.[25][26]

Mating behaviour

The genus Canis contains many different species and has a wide range of different mating systems that varies depending on the type of canine and the species.

Wolves are typically monogamous and form pair-bonds; whereas dogs are promiscuous when free-range and mate with multiple individuals. The study found that in both species females tried to gain access to food more and were more successful in monopolizing a food resource when in heat. Outside of the breeding season their efforts were not as persistent or successful. This shows that the food-for-sex hypothesis likely plays a role in the food sharing among canids and acts as a direct benefit for the females.[27]

Another study on

male-male competition were more aggressive in the presence of high ranking females. This suggests that females prefer dominant males and males prefer high ranking females meaning social cues and status play a large role in the determination of mating pairs in dogs.[28]

Canids also show a wide range of parental care and in 2018 a study showed that sexual conflict plays a role in the determination of intersexual parental investment.[29] The studied looked at coyote mating pairs and found that paternal investment was increased to match or near match the maternal investment. The amount of parental care provided by the fathers also was shown to fluctuated depending on the level of care provided by the mother.

Another study on parental investment showed that in free-ranging dogs, mothers modify their energy and time investment into their pups as they age.[30] Due to the high mortality of free-range dogs at a young age a mother's fitness can be drastically reduced. This study found that as the pups aged the mother shifted from high-energy care to lower-energy care so that they can care for their offspring for a longer duration for a reduced energy requirement. By doing this the mothers increasing the likelihood of their pups surviving infancy and reaching adulthood and thereby increase their own fitness.

A study done in 2017 found that aggression between male and female gray wolves varied and changed with age.[31] Males were more likely to chase away rival packs and lone individuals than females and became increasingly aggressive with age. Alternatively, females were found to be less aggressive and constant in their level of aggression throughout their life. This requires further research but suggests that intersexual aggression levels in gray wolves relates to their mating system.

Tooth breakage

Dentition of a wolf showing functions of the teeth.

Tooth breakage is a frequent result of carnivores' feeding behaviour.[32] Carnivores include both pack hunters and solitary hunters. The solitary hunter depends on a powerful bite at the canine teeth to subdue their prey, and thus exhibits a strong mandibular symphysis. In contrast, a pack hunter, which delivers many shallower bites, has a comparably weaker mandibular symphysis. Thus, researchers can use the strength of the mandibular symphysis in fossil carnivore specimens to determine what kind of hunter it was – a pack hunter or a solitary hunter – and even how it consumed its prey. The mandibles of canids are buttressed behind the carnassial teeth to crack bones with their post-carnassial teeth (molars M2 and M3). A study found that the modern gray wolf and the red wolf (C. rufus) possess greater buttressing than all other extant canids and the extinct dire wolf. This indicates that these are both better adapted for cracking bone than other canids.[33]

A study of nine modern carnivores indicate that one in four adults had suffered tooth breakage and that half of these breakages were of the canine teeth. The highest frequency of breakage occurred in the spotted hyena, which is known to consume all of its prey including the bone. The least breakage occurred in the African wild dog. The gray wolf ranked between these two.[32][34] The eating of bone increases the risk of accidental fracture due to the relatively high, unpredictable stresses that it creates. The most commonly broken teeth are the canines, followed by the premolars, carnassial molars, and incisors. Canines are the teeth most likely to break because of their shape and function, which subjects them to bending stresses that are unpredictable in direction and magnitude.[34] The risk of tooth fracture is also higher when taking and consuming large prey.[34][35]

In comparison to extant gray wolves, the extinct Beringian wolves included many more individuals with moderately to heavily worn teeth and with a significantly greater number of broken teeth. The frequencies of fracture ranged from a minimum of 2% found in the Northern Rocky Mountain wolf (Canis lupus irremotus) up to a maximum of 11% found in Beringian wolves. The distribution of fractures across the tooth row also differs, with Beringian wolves having much higher frequencies of fracture for incisors, carnassials, and molars. A similar pattern was observed in spotted hyenas, suggesting that increased incisor and carnassial fracture reflects habitual bone consumption because bones are gnawed with the incisors and then cracked with the carnassials and molars.[36]

Coyotes, jackals, and wolves

The

the Balkans in Europe.[39]

African migration

The first record of Canis on the African continent is Canis sp. A from South Turkwel, Kenya, dated 3.58–3.2 million years ago.[40] In 2015, a study of mitochondrial genome sequences and whole genome nuclear sequences of African and Eurasian canids indicated that extant wolf-like canids have colonised Africa from Eurasia at least 5 times throughout the Pliocene and Pleistocene, which is consistent with fossil evidence suggesting that much of the African canid fauna diversity resulted from the immigration of Eurasian ancestors, likely coincident with Plio-Pleistocene climatic oscillations between arid and humid conditions.[41]: S1  In 2017, the fossil remains of a new Canis species, named Canis othmanii, was discovered among remains found at Wadi Sarrat, Tunisia, from deposits that date 700,000 years ago. This canine shows a morphology more closely associated with canids from Eurasia instead of Africa.[42]

Gallery

See also

References

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  2. ^ a b Linnæus, Carl (1758). Systema naturæ per regna tria naturæ, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I (in Latin) (10th ed.). Holmiæ (Stockholm): Laurentius Salvius. p. 38. Retrieved November 23, 2015.
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  6. ^ Francis Hemming, ed. (1955). "Direction 22". Opinions and Declarations Rendered by the International Commission on Zoological Nomenclature. Vol. 1C. Order of the International Trust for Zoological Nomenclature. p. 183.
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  15. ^ Rook, L. 1994. The Plio-Pleistocene Old World Canis (Xenocyon) ex gr. falconeri. Bolletino della Società Paleontologica Italiana 33:71–82.
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  19. ^ Cherin, Marco; Bertè, Davide Federico; Sardella, Raffaele; Rook, Lorenzo (2013). "Canis etruscus (Canidae, Mammalia) and its role in the faunal assemblage from Pantalla (Perugia, central Italy): comparison with the Late Villafranchian large carnivore guild of Italy". Bollettino della Società Paleontologica Italiana. 52 (1): 11–18.
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  36. S2CID 14039133. Archived from the original
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  37. ^ "Wolf - Red, Eastern & Ethiopian Wolves, Extinct Falkland Islands & Dire Wolves | Britannica". www.britannica.com. Retrieved 2024-02-24.
  38. ^ Tokar, E. 2001. "Canis latrans" (On-line), Animal Diversity Web. Accessed February 24, 2024 at https://animaldiversity.org/accounts/Canis_latrans/
  39. ^ Parks, Creative Commons Attribution-ShareAlike 4 0 International Thai National. "Canis aureus, Golden jackal". Thai National Parks. Retrieved 2024-02-24.{{cite web}}: CS1 maint: numeric names: authors list (link)
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