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Canis lepophagus

Mammalia - Carnivora - Canidae

Taxonomy
Canis lepophagus was named by Johnston (1938). Its type specimen is West Texas University Museum 881, a skull (skull, lacking mandible), and it is a 3D body fossil. Its type locality is Cita Canyon, which is in a Blancan channel sandstone in Texas.

Sister species lacking formal opinion data

Synonymy list
YearName and author
1938Canis lepophagus Johnston p. 383 figs. Pl. 1 - 3
1980Canis lepophagus Kurten and Anderson p. 167
2008Canis lepophagus Wang et al.
2009Canis lepophagus Tedford et al. p. 112 figs. 40, 41A–G, 42A–J, 43, 44, 52; appendices 2–4
2019Canis lepophagus Albright et al. p. 172

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RankNameAuthor
kingdomAnimalia()
Bilateria
EubilateriaAx 1987
Deuterostomia
phylumChordataHaeckel 1874
subphylumVertebrata
superclassGnathostomata
Osteichthyes()
subclassSarcopterygii()
subclassDipnotetrapodomorpha(Nelson 2006)
subclassTetrapodomorpha()
Tetrapoda
Reptiliomorpha
Anthracosauria
subclassAmphibiosauriaKuhn 1967
Cotylosauria()
Amniota
subclassSynapsida
Therapsida()
infraorderCynodontia()
Mammaliamorpha
Mammaliaformes
RankNameAuthor
classMammalia
Theriamorpha(Rowe 1993)
Theriiformes()
Trechnotheria
Cladotheria
Zatheria
subclassTribosphenida()
subclassTheria
Eutheria()
Placentalia
Boreoeutheria
Laurasiatheria
Scrotifera
Ferae()
CarnivoramorphaWyss and Flynn 1993
CarnivoraformesFlynn et al.
orderCarnivora
familyCanidae
subfamilyCaninaeGill 1872
genusCanis
specieslepophagus

If no rank is listed, the taxon is considered an unranked clade in modern classifications. Ranks may be repeated or presented in the wrong order because authors working on different parts of the classification may disagree about how to rank taxa.

Canis lepophagus Johnston 1938
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Diagnosis
ReferenceDiagnosis
C. S. Johnston 1938
Diagnosis: Canis lepophagus is more slender in its general proportion than the modern coyote. The sagittal and lamb- doidal crests are more prominently developed. The brain case is not expanded, and the postorbital processes are prominent. The lower jaws are strong in proportion to the size of the skull, and the teeth relatively long antero-posteriorly so that the spaces between them are reduced. Furthermore, the C. lepophagus is somewhat smaller than C. latrans as figured by Elliot ( 1901) in which the length of the skull is 201 mm., while in the Cita Canyon specimen the average length for the three skulls is 190 mm. Breadth across the zygomatic arches in the C. latrans is 111 mm. and in the C. tcpophagus 101 mm. However, the ratio of the width to the length is approximately the same in both instances.
R. H. Tedford et al. 2009Derived characters that distinguish C. lepophagus from E. davisi are larger size and more robust skull and jaws; frontal sinus extends more posteriorly; sagittal crest stronger with contribution from frontal; inion narrower and sometimes pointed; m1 talonid with entoconid and hypoconid usually linked by transverse crest; hypoconulid shelf relatively larger but with distinct cusp rarely present; angular process of mandible more robust; and longer forelimb relative to hind- limb (radius/tibia ratio .80% but ,90%).
Canis lepophagus shares the above derived features with C. ferox, but it differs in more consistent m1 hypoconid-entoconid union through cristids, and reduction of M1 para- style.
C. lepophagus differs from many larger species of Canis in its primitively small size; small I3 relative to I1–I2; P4 protocone more anteriorly directed; p4 lacks a posterolingual shelf and is higher than paraconid of m1; m3 retains two trigonid cusps; less inflated frontal sinus; relatively wider frontal shield; and relatively wider braincase.
Primitive characters that distinguish C. lepophagus from C. latrans are: greater postorbital constriction; zygomatic process dorsoventrally deeper with broad scar for masseter muscle; smaller bulla with less laterally extended tubular auditory meatus; P4 protocone situated more anteriorly; m1 less elongate with trigonid shorter relative to length of talonid and weaker hypoconulid; m2 larger relative to m1, metaconid lower crowned, and anterolabial cingulum stron- ger; less elongate limbs especially forelimb, with radius/tibia ratio exceeding 80% but less than that of C. latrans, where ratio usually exceeds 90%.
Measurements
No measurements are available
Composition: phosphaticsubp
Environment: terrestrialsubc
Locomotion: actively mobilec
Life habit: ground dwellingf
Diet: carnivoref
Diet 2: omnivoref
Reproduction: viviparoussubc
Created: 2005-06-08 10:11:09
Modified: 2005-08-22 19:28:06
Source: f = family, subc = subclass, c = class, subp = subphylum
References: Nowak 1991, Lillegraven 1979, Carroll 1988, Ji et al. 2002, Hendy et al. 2009

Age range: base of the Late/Upper Hemphillian to the top of the Gelasian or 10.30000 to 1.80600 Ma

Collections (38 total)


Time interval Ma Country or state Original ID and collection number
Late/Upper Hemphillian10.3 - 4.9USA (Nebraska) Canis lepophagus (18359)
Blancan4.9 - 1.8USA (Nevada) Canis lepophagus (19965)
Blancan4.9 - 1.8USA (Texas) Canidae indet. (20023) Canis lepophagus (type locality: 20033 20034 20050 20060)
Blancan4.9 - 1.8USA (New Mexico) Canis lepophagus (19981)
Blancan4.9 - 1.8USA (California) Canis sp. (19668)
Blancan4.9 - 1.8USA (Idaho) Canis lepophagus (19805 19807 19812 19815 19816 19819 19821 19839 19847 19854 19879 19888 19895 19903 19914)
Blancan4.9 - 1.8USA (Nebraska) Canis lepophagus (19954 19955 19962 19963)
Blancan4.9 - 1.8USA (Washington) Canis lepophagus (20062)
Blancan4.9 - 1.8Mexico (Sonora) Canis rufus (20322)
Blancan4.9 - 1.8USA (Kansas) Canis lepophagus (19932 19934 19940) Canis sp. (19929)
Blancan - Rancholabrean4.9 - 0.012USA (Florida) Canis lepophagus (79621)
Late/Upper Pliocene - Early/Lower Pleistocene3.6 - 0.781USA (Nebraska) Canis lepophagus (197002)
Gelasian2.588 - 1.806USA (Florida) Canis lepophagus (19758)
Early/Lower Pleistocene2.588 - 0.781USA (South Carolina) Canis lepophagus (206955)