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Felidae
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| Felidae[2] | |
|---|---|
| Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Mammalia |
| Order: | Carnivora |
| Superfamily: | Feloidea |
| Family: | Felidae Fischer von Waldheim, 1817 |
| Type genus | |
| Felis | |
| Subfamilies and genera | |
| |
| The native distribution and density of extant felid species. | |
Felidae (/ˈfiːləˌdiː/ FEE-lə-dee[3]) is the family of mammals in the order Carnivora colloquially referred to as cats. A member of this family is also called a felid (/ˈfiːlɪd, -ləd/ FEE-lid, -ləd[4][5]).[6][7][8][9]
The 41 extant Felidae species exhibit the greatest diversity in fur patterns of all terrestrial carnivores.[10] Cats have retractile claws, slender muscular bodies and strong flexible forelimbs. Their teeth and facial muscles allow for a powerful bite. They are all obligate carnivores, and most are solitary predators ambushing or stalking their prey. Wild cats occur in Africa, Europe, Asia and the Americas. Some wild cat species are adapted to forest and savanna habitats, some to arid environments, and a few also to wetlands and mountainous terrain. Their activity patterns range from nocturnal and crepuscular to diurnal, depending on their preferred prey species.[11]
Reginald Innes Pocock divided the extant Felidae into three subfamilies: the Pantherinae, the Felinae and the Acinonychinae, differing from each other by the ossification of the hyoid apparatus and by the cutaneous sheaths which protect their claws.[12] This concept has been revised following developments in molecular biology and techniques for the analysis of morphological data. Today, the living Felidae are divided into two subfamilies: the Pantherinae and Felinae, with the Acinonychinae subsumed into the latter. Pantherinae includes five Panthera and two Neofelis species, while Felinae includes the other 34 species in 12 genera.[13]
The first cats emerged during the Oligocene about 25 million years ago, with the appearance of Proailurus and Pseudaelurus. The latter species complex was ancestral to two main lines of felids: the cats in the extant subfamilies, and the "saber-toothed cats" of the extinct subfamily Machairodontinae, including the famous saber-toothed tiger.
The "false saber-toothed cats", the Barbourofelidae and Nimravidae, are not true cats but are closely related. Together with the Felidae, Viverridae, Nandiniidae, Eupleridae, hyenas and mongooses, they constitute the Feliformia.[14]
Characteristics
[edit]

All members of the cat family have the following characteristics in common:
- They are digitigrade and have five toes on their forefeet and four on their hind feet. Their curved claws are protractile and attached to the terminal bones of the toe with ligaments and tendons. The claws are guarded by cutaneous sheaths, except in the Acinonyx.[15]
- The plantar pads of both fore and hind feet form compact three-lobed cushions.[16]
- They actively protract the claws by contracting muscles in the toe,[11] and they passively retract them. The dewclaws are expanded but do not protract.[17]
- They have lithe and flexible bodies with muscular limbs.[11]
- Their skulls are foreshortened with a rounded profile and large orbits.[17]
- They have 30 teeth with a dental formula of 3.1.3.13.1.2.1. The upper third premolar and lower molar are adapted as carnassial teeth, suited to tearing and cutting flesh.[16] The canine teeth are large, reaching exceptional size in the extinct Machairodontinae. The lower carnassial is smaller than the upper carnassial and has a crown with two compressed blade-like pointed cusps.[11]
- Their tongues are covered with horn-like papillae, which rasp meat from prey and aid in grooming.[17]
- Their noses project slightly beyond the lower jaw.[15]
- Their eyes are relatively large, situated to provide binocular vision. Their night vision is especially good due to the presence of a tapetum lucidum, which reflects light inside the eyeball, and gives felid eyes their distinctive shine. As a result, the eyes of felids are about six times more light-sensitive than those of humans, and many species are at least partially nocturnal. The retina of felids also contains a relatively high proportion of rod cells, adapted for distinguishing moving objects in conditions of dim light, which are complemented by the presence of cone cells for sensing colour during the day.[11]
- They have well-developed and highly sensitive whiskers above the eyes, on the cheeks, and the muzzle, but not below the chin.[15] Whiskers help to navigate in the dark and to capture and hold prey.[17]
- Their external ears are large and especially sensitive to high-frequency sounds in the smaller cat species. This sensitivity allows them to locate small rodent prey.[11]
- The penis is subconical,[15] facing downward when not erect[18] and backward during urination.[19] The baculum is small or vestigial, and shorter than in the Canidae.[18][20] Most felids have penile spines that induce ovulation during copulation.[21]
- They have a vomeronasal organ in the roof of the mouth, allowing them to "taste" the air.[22] The use of this organ is associated with the flehmen response.[23]
- They cannot detect the sweetness of sugar, as they lack the sweet taste receptor.[24]
- They share a broadly similar set of vocalizations but with some variation between species. In particular, the pitch of calls varies, with larger species producing deeper sounds; overall, the frequency of felid calls ranges between 50 and 10,000 hertz.[25][26] The standard sounds made by felids include mewing, chuffing, spitting, hissing, snarling and growling. Mewing and chuffing are the main contact sound, whereas the others signify an aggressive motivation.[11]
- They can purr during both phases of respiration, though pantherine cats seem to purr only during oestrus and copulation, and as cubs when suckling. Purring is generally a low-pitch sound of 16.8–27.5 Hz and is mixed with other vocalization types during the expiratory phase.[27] The ability to roar comes from an elongated and specially adapted larynx and hyoid apparatus.[28] When air passes through the larynx on the way from the lungs, the cartilage walls of the larynx vibrate, producing sound. Only lions, leopards, tigers, and jaguars are truly able to roar, although the loudest mews of snow leopards have a similar, if less structured, sound.[11] Clouded leopards can neither purr nor roar, and so Neofelis is said to be a sister group to Panthera. Sabre-toothed cats may have had the ability to both roar and purr.
The colour, length and density of their fur are very diverse. Fur colour covers the gamut from white to black, and fur patterns from distinctive small spots, and stripes to small blotches and rosettes. Most cat species are born with spotted fur, except the jaguarundi (Herpailurus yagouaroundi), Asian golden cat (Catopuma temminckii) and caracal (Caracal caracal). The spotted fur of lion (Panthera leo), cheetah (Acinonyx jubatus) and cougar (Puma concolor) cubs change to uniform fur during their development to adulthood.[10] Those living in cold environments have thick fur with long hair, like the snow leopard (Panthera uncia) and the Pallas's cat (Otocolobus manul).[17] Those living in tropical and hot climate zones have short fur.[11] Several species exhibit melanism with all-black individuals, cougars are notable for lacking melanism but leucism and albinism are present in cougars along with many other felids.[29]
In the great majority of cat species, the tail is between a third and a half of the body length, although with some exceptions, like the Lynx species and margay (Leopardus wiedii).[11] Cat species vary greatly in body and skull sizes, and weights:
- The largest cat species is the tiger (Panthera tigris), with a head-to-body length of up to 390 cm (150 in), a weight range of at least 65 to 325 kg (143 to 717 lb), and a skull length ranging from 316 to 413 mm (12.4 to 16.3 in).[11][30] Although the maximum skull length of a lion is slightly greater at 419 mm (16.5 in), it is generally smaller in head-to-body length than the tiger.[31]
- The smallest cat species are the rusty-spotted cat (Prionailurus rubiginosus) and the black-footed cat (Felis nigripes). The former is 35–48 cm (14–19 in) in length and weighs 0.9–1.6 kg (2.0–3.5 lb).[11] The latter has a head-to-body length of 36.7–43.3 cm (14.4–17.0 in) and a maximum recorded weight of 2.45 kg (5.4 lb).[32][33]
Most cat species have a haploid number of 18 or 19. Central and South American cats have a haploid number of 18, possibly due to the combination of two smaller chromosomes into a larger one.[34]
Felidae have type IIx muscle fibers three times more powerful than the muscle fibers of human athletes.[35]
Evolution
[edit]
(A) Homotherium latidens (Owen, 1846), specimen DMF AS RS, no. Met-20-1, frozen mummy, Russia, Republic of Sakha (Yakutia), Indigirka River basin, Badyarikha River; Upper Pleistocene;
(B) Panthera leo (Linnaeus, 1758), specimen ZMMU, no. S-210286; Recent.The family Felidae is part of the Feliformia, a suborder that diverged probably about 50.6 to 35 million years ago into several families.[36] The Felidae and the Asiatic linsangs are considered a sister group, which split about 35.2 to 31.9 million years ago.[37]
The earliest cats probably appeared about 35 to 28.5 million years ago. Proailurus is the oldest known cat that occurred after the Eocene–Oligocene extinction event about 33.9 million years ago; fossil remains were excavated in France and Mongolia's Hsanda Gol Formation.[14] Fossil occurrences indicate that the Felidae arrived in North America around 18.5 million years ago. This is about 20 million years later than the bears and the false saber-tooth cats, and about 10 million years later than the canines.[38]
In the Early Miocene about 20 to 16.6 million years ago, Pseudaelurus lived in Africa. Its fossil jaws were also excavated in geological formations of Europe's Vallesian, Asia's Middle Miocene and North America's late Hemingfordian to late Barstovian epochs.[39] Modelling of felid coat pattern transformations revealed that nearly all patterns evolved from small spots.[40]
During the Middle Miocene around 15 million years ago, the extinct subfamily Machairodontinae (colloquially known as "saber-toothed cats") emerged and became widespread across Afro-Eurasia and North America by the Late Miocene.[41][42] With their large upper canine saber teeth, they were adapted to prey on large-bodied megaherbivores.[43][44] During the Late Miocene and early Pliocene, machairodontines were the dominant cats and large mammalian predators across Afro-Eurasia and North America, with ancestors of living cats generally being small at this time.[42]
The earliest members of the living cat lineages are known from the Middle Miocene,[45] with the last common ancestor of living cats estimated to have lived around 16 million years ago.[46] Large sized felines and pantherines only emerged during the Pliocene epoch,[47] including the modern big cat genus Panthera.[48] Felids entered South America as part of the Great American Interchange following the emergence of the Isthmus of Panama during the Pliocene epoch.[49]
Machairodontines began to decline during the Pleistocene, perhaps as a result of environmental change and consequential changes in prey abundance, competition with large living cat lineages such as the pantherins as well as possibly archaic humans. The last species belonging to the genera Smilodon and Homotherium became extinct along with many other large mammals around 12–10,000 years ago as part of the end-Pleistocene extinction event, following human arrival to the Americas at the end of the Late Pleistocene.[50]
Classification
[edit]Traditionally, five subfamilies had been distinguished within the Felidae based on phenotypical features: the Pantherinae, the Felinae, the Acinonychinae,[12] and the extinct Machairodontinae and Proailurinae.[51] Acinonychinae used to only contain the genus Acinonyx but this genus is now within the Felinae subfamily.[13]
Phylogeny
[edit]The following cladogram based on Piras et al. (2013) depicts the phylogeny of basal living and extinct groups.[52]
| Felidae |
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The phylogenetic relationships of living felids are shown in the following cladogram:[53]
| Felidae |
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See also
[edit]References
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- ^ Antón, Mauricio (2013). "Extinctions". Sabertooth. Indiana University Press. pp. 217–230.
- ^ McKenna, M. C.; Bell, S. K. (2000). "Family Felidae Fischer de Waldheim, 1817:372. Cats". Classification of Mammals. Columbia University Press. p. 230. ISBN 978-0-231-11013-6. Archived from the original on 2021-04-19. Retrieved 2020-12-31.
- ^ Piras, P.; Maiorino, L.; Teresi, L.; Meloro, C.; Lucci, F.; Kotsakis, T.; Raia, P. (2013). "Bite of the Cats: Relationships between Functional Integration and Mechanical Performance as Revealed by Mandible Geometry". Systematic Biology. 62 (6): 878–900. doi:10.1093/sysbio/syt053. hdl:11590/132981. ISSN 1063-5157. PMID 23925509.
- ^ Li, G.; Davis, B. W.; Eizirik, E.; Murphy, W. J. (2016). "Phylogenomic evidence for ancient hybridization in the genomes of living cats (Felidae)". Genome Research. 26 (1): 1–11. doi:10.1101/gr.186668.114. PMC 4691742. PMID 26518481.
External links
[edit]- Keller, E. (2015). "Secrets of the World's 38 Species of Wild Cats". National Geographic Society. Archived from the original on 2018-11-13.
Felidae
View on GrokipediaPhysical Characteristics
Anatomy and Morphology
Felids are characterized by a highly specialized body plan adapted for carnivory and predation, featuring a flexible spine composed of approximately 52-53 vertebrae that enables exceptional agility, twisting, and pouncing capabilities.[4] This spinal flexibility is complemented by short, powerful limbs with a digitigrade posture—five toes on the forepaws (including a dewclaw) and four on the hindpaws—allowing for rapid acceleration and precise movements.[5] The musculature is robust and concentrated in the shoulders, back, and hindquarters, providing explosive power for leaping distances up to several times their body length, while the reduced or absent clavicle enhances stride length and forelimb mobility.[6] Most felids possess retractile claws, which are sheathed when not in use to maintain sharpness, though this trait is less developed in cheetahs, lacking a protective fleshy covering.[1] The skull of felids is notably shortened with a reduced rostrum, optimizing the attachment of powerful temporalis and masseter muscles for a bite force that exceeds that of many other carnivores relative to body size.[7] Dentition follows a typical carnassial pattern, with a dental formula of 3/3, 1/1, 3/2-3, 1/1 (yielding 28-30 teeth), featuring elongated, grooved canines for gripping and stabbing prey, small incisors for nipping, and specialized upper premolars and lower molars (carnassials) that shear meat efficiently like scissors.[5] This morphology supports hypercarnivory, with the carnassials adapted for slicing flesh rather than grinding.[1] Felids exhibit significant size variation across the family, ranging from small species like the black-footed cat (Felis nigripes) at 1-2 kg to large pantherines such as the tiger (Panthera tigris) reaching up to 300 kg, influencing proportional features like limb length and skull robustness.[6] Sexual dimorphism is generally modest, with males averaging 5-10% larger in body mass and length than females, though this increases in some species like lions where males can be up to 50% heavier due to enhanced musculature.[5] External features include short, dense fur that varies in length and texture by habitat—longer in temperate species like the Eurasian lynx for insulation—and patterned with rosettes, spots, or stripes for camouflage, such as the jaguar's bold rosettes or the tiger's vertical stripes.[1] Vibrissae, or whiskers, are prominent, stiff sensory hairs arranged in rows on the muzzle, above the eyes, and on the forelegs, embedded deeply with nerve-rich follicles to detect air currents and nearby objects.[1] These morphological traits, including large orbital openings for enhanced vision, underpin sensory adaptations critical for nocturnal hunting.[7]Sensory and Physiological Adaptations
Felids possess highly specialized sensory systems that enhance their predatory efficiency, particularly in low-light conditions and during stealthy pursuits. Their vision is adapted for crepuscular and nocturnal activity, featuring a reflective layer known as the tapetum lucidum behind the retina, which scatters light back through the photoreceptors to amplify photon capture and improve sensitivity in dim environments.[8] This structure, combined with a high density of rod cells—reaching up to approximately 400,000 per square millimeter in the domestic cat retina—enables felids to detect subtle movements in near-darkness.[9] Unlike humans, who are trichromatic, felids exhibit dichromatic color vision mediated by two types of cone cells sensitive primarily to blue-violet and yellow-green wavelengths, with limited discrimination of reds, which appear as shades of gray. Small felids, such as domestic cats and ocelots, further benefit from vertical slit pupils that can constrict to a narrow aperture, optimizing depth perception for precise pouncing on prey within a meter or two by aligning the plane of focus with vertical contours.[10] Hearing in felids is acutely tuned for detecting high-frequency sounds produced by small prey, with large, mobile ear pinnae that swivel independently to pinpoint sound sources directionally. The auditory range extends from about 48 Hz to 85 kHz in domestic cats, far surpassing the human limit of 20 kHz and allowing detection of ultrasonic vocalizations from rodents. Olfaction complements this, supported by an extensive olfactory epithelium containing around 200 million receptor neurons—roughly 40 times more than in humans—enabling discrimination of scents at concentrations as low as parts per billion. The vomeronasal organ, or Jacobson's organ, located in the nasal septum, detects pheromones and non-volatile odorants via a dedicated accessory olfactory system, facilitating behaviors critical to survival such as territory marking and mate selection.[11] Physiologically, felids maintain a high basal metabolic rate, approximately 1.5 times that predicted for similar-sized mammals, reflecting their obligate carnivorous diet and the energetic demands of burst activity during hunts.[12] Their kidneys exhibit exceptional concentrating ability, producing urine with osmolalities up to 3,200 mOsm/L—more than double the human maximum—to conserve water derived primarily from prey moisture, minimizing the need for free water intake.[13] Thermoregulation relies on panting to dissipate heat through evaporative cooling from the respiratory tract and grooming to spread saliva for cutaneous evaporation, adaptations suited to their often arid or variable habitats. These sensory and physiological traits converge in predation adaptations, where night vision acuity is roughly six times greater than humans' in low light, allowing felids to navigate and stalk effectively at dawn or dusk.[14] Rapid neural pathways in the visual and auditory systems enable reflex response times under 50 milliseconds to stimuli, facilitating explosive ambushes with minimal error.Evolutionary History
Origins and Early Evolution
Felidae originated from miacid-like carnivorans within the order Carnivora during the Oligocene epoch, approximately 30–25 million years ago, in Eurasia.[15] These ancestral forms were small, tree-dwelling predators that shared a common miacid heritage with other early carnivorans, evolving specialized traits for hypercarnivory amid the post-Eocene cooling and habitat shifts.[16] The broader divergence of the feliform lineage (including Felidae) from the caniform lineage (such as Canidae) occurred earlier, around 50–40 million years ago in the late Eocene to early Oligocene, establishing the two major suborders of Carnivora.[17] The genus Proailurus represents the earliest recognized true felid, appearing in the late Oligocene of Europe and Asia around 25–30 million years ago.[15] Fossils of Proailurus lemanensis, for instance, exhibit a transitional dentition shifting toward the fully carnivorous sectorial molars characteristic of modern cats, with reduced premolars and enhanced shearing capabilities for processing meat.[18] This genus, small and civet-like in build, foreshadowed key felid innovations such as retractile claws, adapted for climbing and grasping prey in arboreal settings.[19] Evolutionary pressures during this basal phase drove adaptations to forested environments, where dense vegetation favored stealth over endurance running.[15] Early felids like Proailurus likely employed ambush predation strategies, relying on short bursts of speed and powerful limbs for pouncing, rather than the cursorial pursuits seen in contemporaneous canids; this shift is evident in their limb proportions, akin to those of modern forest-dwelling viverrids.[20] Such ecological niches in Oligocene woodlands of Europe promoted the development of flexible skulls and jaws optimized for quick, lethal bites on smaller vertebrates.[21] The Miocene epoch (approximately 23–5 million years ago) witnessed the initial radiation of Felidae, with stem felids such as Pseudaelurus playing a central role in basal diversification across Eurasia and into North America.[22] This genus, emerging around 20 million years ago in the early Miocene, formed a paraphyletic group ancestral to both modern conical-toothed felines and extinct saber-toothed machairodonts, exhibiting generalized body plans suited to varied forested and woodland habitats.[23] The radiation was fueled by global warming and expanding woodlands, enabling felids to exploit new prey resources and spread continentally.[15]Fossil Record and Major Transitions
The fossil record of Felidae reveals a rich history of discoveries that illuminate the family's evolutionary trajectory, particularly through key sites preserving saber-toothed machairodonts. The La Brea Tar Pits in Los Angeles, California, stand out as one of the most prolific localities, containing over 2,000 individuals of Smilodon fatalis from the late Pleistocene (approximately 40,000 to 10,000 years ago), offering unparalleled evidence of their social behavior, injuries, and dietary habits as apex predators in Ice Age ecosystems.[24][25] In North America, early saber-toothed forms are documented from Florida's Central Florida Phosphate Mining District, where fossils of Rhizosmilodon fiteae from the late Hemphillian land-mammal age (about 5 million years ago) represent the oldest known member of the Smilodontini tribe within Machairodontinae.[26] This jaguar-sized cat, known from cranial and dental remains, highlights the initial diversification of specialized saber-tooths in the Pliocene.[26] Asian sites further enrich this record, with the Nihewan Basin in northern China yielding a complete cranium of Homotherium from the early Pleistocene (about 2 million years ago), alongside other machairodont fossils from localities like Yanliang Cave in Guangxi Province, which preserve Megantereon specimens dating to around 2 million years ago and underscore Eurasia's role as a cradle for these lineages.[27][28] Major evolutionary transitions within Felidae are evident in the shift from convergent cat-like forms to true felids with specialized dentition. Nimravids, extinct carnivorans often termed "false saber-tooths," emerged in the late Eocene (around 42 million years ago) and persisted into the late Oligocene, exhibiting early saber-like canines but differing from felids in ear ossicle structure and lacking close phylogenetic ties; they represent a parallel radiation rather than direct ancestry.[29] True felids transitioned to advanced saber-tooth morphology with the rise of the subfamily Machairodontinae in the middle Miocene (approximately 16 million years ago), marked by elongated upper canines up to 20 cm in length for slashing prey, as seen in genera like Machairodus. This innovation drove diversification, with key splits such as the divergence between Smilodon and Homotherium lineages occurring around 18 million years ago, enabling adaptation to large herbivores across continents.[30] These forms contrasted with the conical-toothed Felinae, which emphasized cursorial hunting and would later dominate post-extinction faunas. The Pleistocene megafauna extinction event around 12,000 years ago marked a pivotal transition, wiping out all machairodonts while sparing conical-toothed felines. Saber-toothed cats like Smilodon fatalis and Homotherium latidens vanished abruptly at the end of the Pleistocene, not from starvation—as evidenced by stable dental microwear indicating consistent meat diets until the end—but likely from cascading effects of climate warming, habitat loss, and human hunting pressures that disrupted megafaunal prey bases.[31][30] This die-off eliminated the specialized saber-tooth niche, allowing Felinae survivors to radiate into diverse modern roles without competition from these ambush specialists. Felidae's Neogene diversification included critical dispersals to the Americas via land bridges, facilitating global spread. Originating in Eurasia, early felids crossed the Bering Land Bridge into North America around 20 million years ago during the Miocene, with subsequent waves enabling southward migration. By approximately 7 million years ago, proto-Panamanian connections in the late Miocene allowed initial incursions into South America, introducing machairodonts and conical-toothed forms that underwent regional adaptation and contributed to the Great American Biotic Interchange's carnivoran component.[32] This expansion wave set the stage for New World saber-tooths like Smilodon to thrive until the Pleistocene extinctions.Taxonomy and Classification
Subfamilies and Phylogeny
The taxonomy of Felidae traces its origins to Carl Linnaeus's Systema Naturae (1758), where he classified all known cats under the single genus Felis, encompassing species such as the domestic cat (Felis catus) and lion (Felis leo). This Linnaean framework persisted with modifications through the 19th and 20th centuries, but major revisions began in the post-2000s era, driven by molecular genetic analyses that resolved longstanding uncertainties in evolutionary relationships. These studies integrated mitochondrial DNA (mtDNA) sequences, such as from cytochrome b and 16S rRNA genes, with nuclear markers including autosomal, X-linked, and Y-linked loci, providing robust evidence for clade monophyly and divergence timings. Felidae is classified into two extant subfamilies: Pantherinae (big cats, including genera Panthera and Neofelis, such as the lion Panthera leo and tiger Panthera tigris) and Felinae (small cats, encompassing the remaining genera), which form sister clades.[3] Pantherine cats are distinguished by their ability to roar, enabled by an elastic ligamentous hyoid apparatus that allows greater laryngeal mobility, in contrast to the fully ossified hyoid in felines that supports purring but prevents roaring.[33] Molecular phylogenies further delineate eight principal extant lineages within Felidae, reflecting a rapid Miocene radiation: the Panthera lineage (roaring cats, including the lion (Panthera leo) and tiger (Panthera tigris) in the genus Panthera, and clouded leopards in Neofelis), bay cat lineage (Pardofelis and Catopuma), caracal lineage (Caracal and Leptailurus), ocelot lineage (Leopardus), lynx lineage (Lynx), puma lineage (Puma, Acinonyx, and Herpailurus), domestic cat lineage (Felis), and leopard cat lineage (Prionailurus and Otocolobus). Within the genus Panthera, a common phylogenetic topology places the tiger as sister to a clade containing the snow leopard (Panthera uncia), leopard (Panthera pardus), lion (Panthera leo), and jaguar (Panthera onca), with lion and jaguar forming a sister pair in many studies.[34] The leopard cat (Prionailurus bengalensis) and lynxes (genus Lynx) belong to separate lineages within Felinae (the leopard cat lineage and lynx lineage, respectively) and are more distantly related to each other than to species in Pantherinae. The domestic cat (Felis catus) is firmly placed within the Felis lineage of Felinae, confirmed by mtDNA and nuclear gene analyses showing its close relation to wildcats like the European wildcat (Felis silvestris). Felidae forms a monophyletic group within the suborder Feliformia, which represents the basal split from Caniformia approximately 42.6 million years ago (Ma) in the Eocene.[35] Within Felidae, the divergence between Pantherinae and Felinae occurred around 10.8 Ma during the late Miocene, followed by sequential splits among the seven Felinae lineages between 9.4 Ma and 6.2 Ma, as evidenced by Bayesian analyses of multi-locus datasets calibrated with fossil constraints. These timings align with paleoenvironmental shifts, such as cooling climates and habitat fragmentation, that promoted felid diversification; for instance, Y-chromosome markers proved particularly informative for resolving deep nodes, outperforming mtDNA in phylogenetic signal strength. Subsequent species-level radiations within lineages occurred primarily in the Pliocene-Pleistocene (3.1–0.7 Ma), further validated by genome-wide SNP data from over 22,000 base pairs across cat species.| Lineage | Subfamily | Representative Genera | Key Divergence Time (Ma) |
|---|---|---|---|
| Panthera | Pantherinae | Panthera, Neofelis | ~10.8 (basal to Felidae radiation) |
| Bay cat | Felinae | Pardofelis, Catopuma | ~9.4 |
| Caracal | Felinae | Caracal, Leptailurus | ~8.5 |
| Ocelot | Felinae | Leopardus | ~8.0 |
| Lynx | Felinae | Lynx | ~7.2 |
| Puma | Felinae | Puma, Acinonyx, Herpailurus | ~6.7 |
| Domestic cat | Felinae | Felis | ~6.2 |
| Leopard cat | Felinae | Prionailurus, Otocolobus | ~5.9 |