fbpx
Wikipedia

Smilodon

Smilodon is a genus of felids belonging to the extinct subfamily Machairodontinae. It is one of the best known saber-toothed predators and prehistoric mammals. Although commonly known as the saber-toothed tiger, it was not closely related to the tiger or other modern cats. Smilodon lived in the Americas during the Pleistocene epoch (2.5 mya – 10,000 years ago). The genus was named in 1842 based on fossils from Brazil; the generic name means "scalpel" or "two-edged knife" combined with "tooth". Three species are recognized today: S. gracilis, S. fatalis, and S. populator. The two latter species were probably descended from S. gracilis, which itself probably evolved from Megantereon. The hundreds of specimens obtained from the La Brea Tar Pits in Los Angeles constitute the largest collection of Smilodon fossils.

Smilodon
Temporal range: Early Pleistocene to Early Holocene, 2.5–0.01 Ma
Mounted S. populator skeleton at Tellus Science Museum
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Suborder: Feliformia
Family: Felidae
Subfamily: Machairodontinae
Tribe: Smilodontini
Genus: Smilodon
Lund, 1842
Type species
Smilodon populator
Lund, 1842
Other species
  • S. fatalis Leidy, 1869
  • S. gracilis Cope, 1880
Synonyms
Genus synonymy
  • Munifelis Muñis, 1845
  • Trucifelis Leidy, 1868
  • Smilodontopsis Brown, 1908
  • Prosmilodon Rusconi, 1929
  • Smilodontidion Kraglievich, 1948
Species synonymy
  • S. populator:
    • Munifelis bonaerensis Muñis, 1845
    • Smilodon blainvillii Desmarest, 1860
    • Machaerodus bonaerensis Burmeister, 1867
    • Machaerodus necator Gervais, 1878
    • Smilodon ensenadensis Ameghino, 1888
    • Machaerodus ensenadensis Ameghino, 1889
    • Smilodon crucians Ameghino, 1904
    • Smilodon bonaerensis Ameghino, 1907
    • Smilodon neogaeus ensenadensis Boule & Thévenin, 1920
    • Smilodon (Prosmilodon) ensenadensis Rusconi, 1929
    • Smilodon neogaeus de Paula Couto, 1940
    • Smilodon necator de Paula Couto, 1940
    • Smilodon (Prosmilodon) ensenadensis ferox Kraglievich, 1947
    • Smilodon (Prosmilodon) ensenadensis minor Kraglievich, 1948
    • Smilodontidion riggii Kraglievich, 1948
    • Machaerodus neogaeus Pictet, 1953
    • Felis smilodon Desmarest, 1953
    • Smilodon populator populator de Paula Couto, 1955
  • S. fatalis:
    • Felis (Trucifelis) fatalis Leidy, 1868
    • Trucifelis fatalis Leidy, 1869
    • Machaerodus fatalis Lydekker, 1884
    • Drepanodon floridanus Leidy, 1889
    • Machaerodus floridanus Leidy, 1889
    • Uncia mercerii Cope, 1895
    • Smilodon floridanus Adams, 1896
    • Machaerodus (Smilodon) mercerii Cope, 1899
    • Smilodon californicus Bovard, 1907
    • Smilodontopsis troglodytes Brown, 1908
    • Smilodontopsis conardi Brown, 1908
    • Smilodontopsis mercerii Brown, 1908
    • Smilodon nebraskensis Matthew, 1918
    • Machaerodus mercerii Matthew, 1918
    • Smilodon (Trucifelis) californicus Merriam & Stock, 1932
    • Smilodon (Trucifelis) fatalis Merriam & Stock, 1932
    • Smilodon (Trucifelis) nebraskensis Merriam & Stock, 1932
    • Smilodon (Trucifelis) californicus brevipes Merriam & Stock, 1932
    • Smilodon trinitensis Slaughter, 1960
  • S. gracilis:
    • Machaerodus (Smilodon) gracilis Cope, 1899
    • Smilodon (Smilodontopsis) gracilis Merriam & Stock, 1932
    • Megantereon gracilis Broom & Schepers 1946
    • Ischyrosmilus gracilis Churcher, 1984
    • Smilodontopsis gracilis Berta, 1995

Overall, Smilodon was more robustly built than any extant cat, with particularly well-developed forelimbs and exceptionally long upper canine teeth. Its jaw had a bigger gape than that of modern cats, and its upper canines were slender and fragile, being adapted for precision killing. S. gracilis was the smallest species at 55 to 100 kg (120 to 220 lb) in weight. S. fatalis had a weight of 160 to 280 kg (350 to 620 lb) and height of 100 cm (39 in). Both of these species are mainly known from North America, but remains from South America have also been attributed to them. S. populator from South America was the largest species, at 220 to 436 kg (485 to 961 lb) in weight and 120 cm (47 in) in height, and was among the largest known felids. The coat pattern of Smilodon is unknown, but it has been artistically restored with plain or spotted patterns.

In North America, Smilodon hunted large herbivores such as bison and camels, and it remained successful even when encountering new prey species in South America. Smilodon is thought to have killed its prey by holding it still with its forelimbs and biting it, but it is unclear in what manner the bite itself was delivered. Scientists debate whether Smilodon had a social or a solitary lifestyle; analysis of modern predator behavior as well as of Smilodon's fossil remains could be construed to lend support to either view. Smilodon probably lived in closed habitats such as forests and bush, which would have provided cover for ambushing prey. Smilodon died out at the same time that most North and South American megafauna disappeared, about 10,000 years ago. Its reliance on large animals has been proposed as the cause of its extinction. S. fatalis may have been impacted by habitat turnover and loss of prey it specialized on due to possible climatic plus anthropogenic impacts and other factors while the extinction of S. populator remains poorly understood.

Taxonomy edit

 
S. populator skull and syntype canine from Lund's collection, Zoological Museum, Copenhagen

During the 1830s, Danish naturalist Peter Wilhelm Lund and his assistants collected fossils in the calcareous caves near the small town of Lagoa Santa, Minas Gerais, Brazil. Among the thousands of fossils found, he recognized a few isolated cheek teeth as belonging to a hyena, which he named Hyaena neogaea in 1839. After more material was found (including canine teeth and foot bones), Lund concluded the fossils instead belonged to a distinct genus of felids, though transitional to the hyenas. He stated it would have matched the largest modern predators in size, and was more robust than any modern cat. Lund originally wanted to name the new genus Hyaenodon, but realizing this had recently become preoccupied by another prehistoric predator, he instead named it Smilodon populator in 1842. He explained the Ancient Greek meaning of Smilodon as σμίλη (smilē), "scalpel" or "two-edged knife", and οδόντος (odóntos), "tooth". This has also been translated as "tooth shaped like double-edged knife". He explained the species name populator as "the destroyer", which has also been translated as "he who brings devastation". By 1846, Lund had acquired nearly every part of the skeleton (from different individuals), and more specimens were found in neighboring countries by other collectors in the following years.[1][2] Though some later authors used Lund's original species name neogaea instead of populator, it is now considered an invalid nomen nudum, as it was not accompanied with a proper description and no type specimens were designated.[3] Some South American specimens have been referred to other genera, subgenera, species, and subspecies, such as Smilodontidion riggii, Smilodon (Prosmilodon) ensenadensis, and S. bonaeriensis, but these are now thought to be junior synonyms of S. populator.[4]

 
1869 lithograph of the holotype molar and maxilla fragment of S. fatalis

Fossils of Smilodon were discovered in North America from the second half of the 19th century onwards.[1] In 1869, American paleontologist Joseph Leidy described a maxilla fragment with a molar, which had been discovered in a petroleum bed in Hardin County, Texas. He referred the specimen to the genus Felis (which was then used for most cats, extant as well as extinct) but found it distinct enough to be part of its own subgenus, as F. (Trucifelis) fatalis.[5] The species name means "deadly".[6] In an 1880 article about extinct American cats, American paleontologist Edward Drinker Cope pointed out that the F. fatalis molar was identical to that of Smilodon, and he proposed the new combination S. fatalis.[7] Most North American finds were scanty until excavations began in the La Brea Tar Pits in Los Angeles, where hundreds of individuals of S. fatalis have been found since 1875.[1] S. fatalis has junior synonyms such as S. mercerii, S. floridanus, and S. californicus.[4] American paleontologist Annalisa Berta considered the holotype of S. fatalis too incomplete to be an adequate type specimen, and the species has at times been proposed to be a junior synonym of S. populator.[3] Nordic paleontologists Björn Kurtén and Lars Werdelin supported the distinctness of the two species in an article published in 1990.[8] A 2018 article by the American paleontologist John P. Babiarz and colleagues concluded that S. californicus, represented by the specimens from the La Brea Tar Pits, was a distinct species from S. fatalis after all and that more research is needed to clarify the taxonomy of the lineage.[9]

In his 1880 article about extinct cats, Cope also named a third species of Smilodon, S. gracilis. The species was based on a partial canine, which had been obtained in the Port Kennedy Cave near the Schuylkill River in Pennsylvania. Cope found the canine to be distinct from that of the other Smilodon species due to its smaller size and more compressed base.[7] Its specific name refers to the species' lighter build.[10] This species is known from fewer and less complete remains than the other members of the genus.[11] S. gracilis has at times been considered part of genera such as Megantereon and Ischyrosmilus.[12] S. populator, S. fatalis and S. gracilis are currently considered the only valid species of Smilodon, and features used to define most of their junior synonyms have been dismissed as variation between individuals of the same species (intraspecific variation).[4][3] One of the most famous of prehistoric mammals, Smilodon has often been featured in popular media and is the state fossil of California.[1]

Evolution edit

 
Partial skull of S. gracilis, the earliest species in the genus, Academy of Natural Sciences of Philadelphia

Long the most completely known saber-toothed cat, Smilodon is still one of the best-known members of the group, to the point where the two concepts have been confused. The term "saber-tooth" itself refers to an ecomorph consisting of various groups of extinct predatory synapsids (mammals and close relatives), which convergently evolved extremely long maxillary canines, as well as adaptations to the skull and skeleton related to their use. This includes members of Gorgonopsia, Thylacosmilidae, Machaeroidinae, Nimravidae, Barbourofelidae, and Machairodontinae.[1][13] Within the family Felidae (true cats), members of the subfamily Machairodontinae are referred to as saber-toothed cats, and this group is itself divided into three tribes: Metailurini (false saber-tooths); Homotherini (scimitar-toothed cats); and Smilodontini (dirk-toothed cats), to which Smilodon belongs.[4] Members of Smilodontini are defined by their long slender canines with fine to no serrations, whereas Homotherini are typified by shorter, broad, and more flattened canines, with coarser serrations.[14] Members of Metailurini were less specialized and had shorter, less flattened canines, and are not recognized as members of Machairodontinae by some researchers.[4]

The earliest felids are known from the Oligocene of Europe, such as Proailurus, and the earliest one with saber-tooth features is the Miocene genus Pseudaelurus.[4] The skull and mandible morphology of the earliest saber-toothed cats was similar to that of the modern clouded leopards (Neofelis). The lineage further adapted to the precision killing of large animals by developing elongated canine teeth and wider gapes, in the process sacrificing high bite force.[15] As their canines became longer, the bodies of the cats became more robust for immobilizing prey.[14] In derived smilodontins and homotherins, the lumbar region of the spine and the tail became shortened, as did the hind limbs.[4] Based on mitochondrial DNA sequences extracted from fossils, the lineages of Homotherium and Smilodon are estimated to have diverged about 18 Ma ago.[16]

The earliest species of Smilodon is S. gracilis, which existed from 2.5 million to 500,000 years ago (early Blancan to Irvingtonian ages) and was the successor in North America of Megantereon, from which it probably evolved. Megantereon itself had entered North America from Eurasia during the Pliocene, along with Homotherium. S. gracilis reached the northern regions of South America in the Early Pleistocene as part of the Great American Interchange.[17][14] S. fatalis existed 1.6 million–10,000 years ago (late Irvingtonian to Rancholabrean ages), and replaced S. gracilis in North America.[8] S. populator existed 1 million–10,000 years ago (Ensenadan to Lujanian ages); it occurred in the eastern parts of South America.[18]

Despite the colloquial name "saber-toothed tiger", Smilodon is not closely related to the modern tiger (which belongs in the subfamily Pantherinae), or any other extant felid.[19] A 1992 ancient DNA analysis suggested that Smilodon should be grouped with modern cats (subfamilies Felinae and Pantherinae).[20] A 2005 study found that Smilodon belonged to a separate lineage.[21] A study published in 2006 confirmed this, showing that the Machairodontinae diverged early from the ancestors of modern cats and were not closely related to any living species.[22] The following cladogram based on fossils and DNA analysis shows the placement of Smilodon among extinct and extant felids, after Rincón and colleagues, 2011:[17]

 
S. fatalis skeleton at National Museum of Natural History
 
S. populator statue in Tierpark Berlin
Felidae

Proailurus

Pseudaelurus

Pantherinae

Panthera (tigers, lions, jaguars, and leopards) 

Felinae

Caracal 

Leopardus (ocelot and relatives) 

Felis (domestic cats and relatives) 

Herpailurus (jaguarundi)  

Miracinonyx  

Puma (cougar) 

Machairodontinae

Dinofelis  

Paramachairodus

Megantereon

Smilodon gracilis 

Smilodon populator 

Smilodon fatalis 

Description edit

 
Size of the three Smilodon species compared to a human

Skeleton edit

Smilodon was around the size of modern big cats, but was more robustly built. It had a reduced lumbar region, high scapula, short tail, and broad limbs with relatively short feet.[23][24] Smilodon is most famous for its relatively long canine teeth, which are the longest found in the saber-toothed cats, at about 28 cm (11 in) long in the largest species, S.populator.[23] The canines were slender and had fine serrations on the front and back side.[25] The skull was robustly proportioned and the muzzle was short and broad. The cheek bones (zygomata) were deep and widely arched, the sagittal crest was prominent, and the frontal region was slightly convex. The mandible had a flange on each side of the front. The upper incisors were large, sharp, and slanted forwards. There was a diastema (gap) between the incisors and molars of the mandible. The lower incisors were broad, recurved, and placed in a straight line across. The p3 premolar tooth of the mandible was present in most early specimens, but lost in later specimens; it was only present in 6% of the La Brea sample.[3] There is some dispute over whether Smilodon was sexually dimorphic. Some studies of S. fatalis fossils have found little difference between the sexes.[26][27] Conversely, a 2012 study found that, while fossils of S. fatalis show less variation in size among individuals than modern Panthera, they do appear to show the same difference between the sexes in some traits.[28]

S. gracilis was the smallest species, estimated at 55 to 100 kg (120 to 220 lb) in weight, about the size of a jaguar. It was similar to its predecessor Megantereon of the same size, but its dentition and skull were more advanced, approaching S. fatalis.[29][4] S. fatalis was intermediate in size between S. gracilis and S. populator.[23] It ranged from 160 to 280 kg (350 to 620 lb).[29] and reached a shoulder height of 100 cm (39 in) and body length of 175 cm (69 in).[30] It was similar to a lion in dimensions, but was more robust and muscular, and therefore had a larger body mass. Its skull was also similar to that of Megantereon, though more massive and with larger canines.[4] S. populator was among the largest known felids, with a body mass range from 220 kg (490 lb) to over 400 kg (880 lb),[29] and one estimate suggesting up to 470 kg (1,040 lb).[31] A particularly large S. populator skull from Uruguay measuring 39.2 cm (15.4 in) in length indicates this individual may have weighed as much as 436 kg (961 lb).[32] It stood at a shoulder height of 120 cm (47 in).[23] Compared to S. fatalis, S. populator was more robust and had a more elongated and narrow skull with a straighter upper profile, higher positioned nasal bones, a more vertical occiput, more massive metapodials and slightly longer forelimbs relative to hindlimbs.[4][8] Large fossil tracks from Argentina (for which the ichnotaxon name Smilodonichium has been proposed) have been attributed to S. populator, and measure 17.6 cm (6.9 in) by 19.2 cm (7.6 in).[33] This is larger than tracks of the Bengal tiger, to which the footprints have been compared.[34]

External features edit

 
 
S. populator restored with plain coat by Charles R. Knight in 1903 (left), and S. fatalis restored with spotted coat (right), both of which are considered possibilities

Smilodon and other saber-toothed cats have been reconstructed with both plain-colored coats and with spotted patterns (which appears to be the ancestral condition for feliforms), both of which are considered possible.[35] Studies of modern cat species have found that species that live in the open tend to have uniform coats while those that live in more vegetated habitats have more markings, with some exceptions.[36] Some coat features, such as the manes of male lions or the stripes of the tiger, are too unusual to predict from fossils.[35]

Traditionally, saber-toothed cats have been artistically restored with external features similar to those of extant felids, by artists such as Charles R. Knight in collaboration with various paleontologists in the early 20th century.[35] In 1969, paleontologist G. J. Miller instead proposed that Smilodon would have looked very different from a typical cat and similar to a bulldog, with a lower lip line (to allow its mouth to open wide without tearing the facial tissues), a more retracted nose and lower-placed ears.[37] Paleoartist Mauricio Antón and coauthors disputed this in 1998 and maintained that the facial features of Smilodon were overall not very different from those of other cats. Antón noted that modern animals like the hippopotamus are able to open their mouths extremely wide without tearing tissue due to a folded orbicularis oris muscle, and such a muscle arrangement exists in modern large felids.[38] Antón stated that extant phylogenetic bracketing (where the features of the closest extant relatives of a fossil taxon are used as reference) is the most reliable way of restoring the life-appearance of prehistoric animals, and the cat-like Smilodon restorations by Knight are therefore still accurate.[35] A 2022 study by Antón and colleagues concluded that the upper canines of Smilodon would have been visible when the mouth was closed, while those of Homotherium would have not, after examining fossils and extant big cats.[39]

Paleobiology edit

Diet edit

 
S. populator canine tooth; the tip points to the right

An apex predator, Smilodon primarily hunted large mammals. Isotopes preserved in the bones of S. fatalis in the La Brea Tar Pits reveal that ruminants like bison (Bison antiquus, which was much larger than the modern American bison) and camels (Camelops) were most commonly taken by the cats there.[40]Smilodon fatalis may have also occasionally preyed upon Glyptotherium, based on a skull from a juvenile Glyptotherium texanum recovered from Pleistocene deposits in Arizona that bear the distinctive elliptical puncture marks best matching those of Smilodon, indicating that the predator successfully bit into the skull through the glyptodont's armored cephalic shield.[41] In addition, isotopes preserved in the tooth enamel of S. gracilis specimens from Florida show that this species fed on the peccary Platygonus and the llama-like Hemiauchenia.[42] Stable carbon isotope measurements of S. gracilis remains in Florida varied significantly between different sites and show that the species was flexible in its feeding habits.[43] Isotopic studies of dire wolf (Aenocyon dirus) and American lion (Panthera atrox) bones show an overlap with S. fatalis in prey, which suggests that they were competitors.[40] More detailed isotope analysis however, indicates that Smilodon fatalis preferred forest-dwelling prey such as tapirs, deer and forest-dwelling bison as opposed to the dire wolves' preferences for prey inhabiting open areas such as grassland.[44] The availability of prey in the Rancho La Brea area was likely comparable to modern East Africa.[45]

 
Two S. populator stalking a Palaeolama group in Brazil

As Smilodon migrated to South America, its diet changed; bison were absent, the horses and proboscideans were different, and native ungulates such as toxodonts and litopterns were completely unfamiliar, yet S. populator thrived as well there as its relatives in North America.[14] Isotopic analysis for S. populator suggests that its main prey species included Toxodon platensis, Pachyarmatherium, Holmesina, species of the genus Panochthus, Palaeolama, Catonyx, Equus neogeus, and the crocodilian Caiman latirostris. This analysis of its diet also indicates that S. populator hunted both in open and forested habitats.[46] The differences between the North and South American species may be due to the difference in prey between the two continents.[8] Smilodon may have avoided eating bone and would have left enough food for scavengers.[47] Coprolites assigned to S. populator recovered from Argentina preserve Mylodon osteoderms and a Lama scaphoid bone. In addition to this unambiguous evidence of bone consumption, the coprolites suggest that Smilodon had a more generalist diet than previously thought.[48] Examinations of dental microwear from La Brea further suggests that Smilodon consumed both flesh and bone.[49] Smilodon itself may have scavenged dire wolf kills.[50] It has been suggested that Smilodon was a pure scavenger that used its canines for display to assert dominance over carcasses, but this theory is not supported today as no modern terrestrial mammals are pure scavengers.[51]

Predatory behavior edit

 
Tracks from Argentina which may have been produced by Smilodon

The brain of Smilodon had sulcal patterns similar to modern cats, which suggests an increased complexity of the regions that control the sense of hearing, sight, and coordination of the limbs. Felid saber-tooths in general had relatively small eyes that were not as forward-facing as those of modern cats, which have good binocular vision to help them move in trees.[51] Smilodon was likely an ambush predator that concealed itself in dense vegetation, as its limb proportions were similar to modern forest-dwelling cats,[52] and its short tail would not have helped it balance while running.[53] Unlike its ancestor Megantereon, which was at least partially scansorial and therefore able to climb trees, Smilodon was probably completely terrestrial due to its greater weight and lack of climbing adaptations.[54] Tracks from Argentina named Felipeda miramarensis in 2019 may have been produced by Smilodon. If correctly identified, the tracks indicate that the animal had fully retractible claws, plantigrade feet, lacked strong supination capabilities in its paws, notably robust forelimbs compared to the hindlimbs, and was probably an ambush predator.[55]

The heel bone of Smilodon was fairly long, which suggests it was a good jumper.[23] Its well-developed flexor and extensor muscles in its forearms probably enabled it to pull down, and securely hold down, large prey. Analysis of the cross-sections of S. fatalis humeri indicated that they were strengthened by cortical thickening to such an extent that they would have been able to sustain greater loading than those of extant big cats, or of the extinct American lion. The thickening of S. fatalis femurs was within the range of extant felids.[56] Its canines were fragile and could not have bitten into bone; due to the risk of breaking, these cats had to subdue and restrain their prey with their powerful forelimbs before they could use their canine teeth, and likely used quick slashing or stabbing bites rather than the slow, suffocating bites typically used by modern cats.[56] On rare occasions, as evidenced by fossils, Smilodon was willing to risk biting into bone with its canines. This may have been focused more towards competition such as other Smilodon or potential threats such as other carnivores than on prey.[54]

 
Maximum gape of a saber-toothed cat (A) and reconstructions of neck bite in prey of different sizes (B, C)

Debate continues as to how Smilodon killed its prey. Traditionally, the most popular theory is that the cat delivered a deep stabbing bite or open-jawed stabbing thrust to the throat, killing the prey very quickly.[56][57] Another hypothesis suggests that Smilodon targeted the belly of its prey. This is disputed, as the curvature of their prey's belly would likely have prevented the cat from getting a good bite or stab.[58] In regard to how Smilodon delivered its bite, the "canine shear-bite" hypothesis has been favored, where flexion of the neck and rotation of the skull assisted in biting the prey, but this may be mechanically impossible. However, evidence from comparisons with Homotherium suggest that Smilodon was fully capable of and utilized the canine shear-bite as its primary means of killing prey, based on the fact that it had a thick skull and relatively little trabecular bone, while Homotherium had both more trabecular bone and a more lion-like clamping bite as its primary means of attacking prey. The discovery, made by Figueirido and Lautenschlager et al., published in 2018 suggests extremely different ecological adaptations in both machairodonts.[59] The mandibular flanges may have helped resist bending forces when the mandible was pulled against the hide of a prey animal.[60]

 
 
S. fatalis skull cast (left) and restoration by Mauricio Antón showing a wide gape

The protruding incisors were arranged in an arch, and were used to hold the prey still and stabilize it while the canine bite was delivered. The contact surface between the canine crown and the gum was enlarged, which helped stabilize the tooth and helped the cat sense when the tooth had penetrated to its maximum extent. Since saber-toothed cats generally had a relatively large infraorbital foramen (opening) in the skull, which housed nerves associated with the whiskers, it has been suggested the improved senses would have helped the cats' precision when biting outside their field of vision, and thereby prevent breakage of the canines. The blade-like carnassial teeth were used to cut skin to access the meat, and the reduced molars suggest that they were less adapted for crushing bones than modern cats.[51] As the food of modern cats enters the mouth through the side while cutting with the carnassials, not the front incisors between the canines, the animals do not need to gape widely, so the canines of Smilodon would likewise not have been a hindrance when feeding.[38] A study published in 2022 of how machairodonts fed revealed that wear patterns on the teeth of S. fatalis also suggest that it was capable of eating bone to a similar extent as lions. This and comparisons with bite marks left by the contemporary machairodont Xenosmilus suggest that Smilodon and its relatives could efficiently de-flesh a carcass of meat when feeding without being hindered by their long canines.[61]

Despite being more powerfully built than other large cats, Smilodon had a weaker bite. Modern big cats have more pronounced zygomatic arches, while these were smaller in Smilodon, which restricted the thickness and therefore power of the temporalis muscles and thus reduced Smilodon's bite force. Analysis of its narrow jaws indicates that it could produce a bite only a third as strong as that of a lion (the bite force quotient measured for the lion is 112).[62][63] There seems to be a general rule that the saber-toothed cats with the largest canines had proportionally weaker bites. Analyses of canine bending strength (the ability of the canine teeth to resist bending forces without breaking) and bite forces indicate that the saber-toothed cats' teeth were stronger relative to the bite force than those of modern big cats.[64] In addition, Smilodon's gape could have reached over 110 degrees,[65] while that of the modern lion reaches 65 degrees.[66] This made the gape wide enough to allow Smilodon to grasp large prey despite the long canines.[38] A 2018 study compared the killing behavior of Smilodon fatalis and Homotherium serum, and found that the former had a strong skull with little trabecular bone for a stabbing canine-shear bite, whereas the latter had more trabecular bone and used a clamp and hold style more similar to lions. The two would therefore have held distinct ecological niches.[67]

Natural traps edit

 
S. fatalis fighting dire wolves over a Columbian mammoth carcass in the La Brea Tar Pits, by Robert Bruce Horsfall, 1913

Many Smilodon specimens have been excavated from asphalt seeps that acted as natural carnivore traps. Animals were accidentally trapped in the seeps and became bait for predators that came to scavenge, but these were then trapped themselves. The best-known of such traps are at La Brea in Los Angeles, which have produced over 166,000 Smilodon fatalis specimens[68] that form the largest collection in the world. The sediments of the pits there were accumulated 40,000 to 10,000 years ago, in the Late Pleistocene. Though the trapped animals were buried quickly, predators often managed to remove limb bones from them, but they were themselves often trapped and then scavenged by other predators; 90% of the excavated bones belonged to predators.[69]

The Talara Tar Seeps in Peru represent a similar scenario, and have also produced fossils of Smilodon. Unlike in La Brea, many of the bones were broken or show signs of weathering. This may have been because the layers were shallower, so the thrashing of trapped animals damaged the bones of previously trapped animals. Many of the carnivores at Talara were juveniles, possibly indicating that inexperienced and less fit animals had a greater chance of being trapped. Though Lund thought accumulations of Smilodon and herbivore fossils in the Lagoa Santa Caves were due to the cats using the caves as dens, these are probably the result of animals dying on the surface, and water currents subsequently dragging their bones to the floor of the cave, but some individuals may also have died after becoming lost in the caves.[69]

Social life edit

 
S. fatalis pair approaching a group of the ground sloth Paramylodon, one mired, at the La Brea Tar Pits, by Knight, 1921

Scientists debate whether Smilodon was social. One study of African predators found that social predators like lions and spotted hyenas respond more to the distress calls of prey than solitary species. Since S. fatalis fossils are common at the La Brea Tar Pits, and were likely attracted by the distress calls of stuck prey, this could mean that this species was social as well.[70] One critical study claims that the study neglects other factors, such as body mass (heavier animals are more likely to get stuck than lighter ones), intelligence (some social animals, like the American lion, may have avoided the tar because they were better able to recognize the hazard), lack of visual and olfactory lures, the type of audio lure, and the length of the distress calls (the actual distress calls of the trapped prey animals would have lasted longer than the calls used in the study). The author of that study ponders what predators would have responded if the recordings were played in India, where the otherwise solitary tigers are known to aggregate around a single carcass.[71] The authors of the original study responded that though effects of the calls in the tar pits and the playback experiments would not be identical, this would not be enough to overturn their conclusions. In addition, they stated that weight and intelligence would not likely affect the results as lighter carnivores are far more numerous than heavy herbivores and the social (and seemingly intelligent) dire wolf is also found in the pits.[72]

 
Lion pride attacking an African buffalo in Tanzania; Smilodon may also have hunted in groups

Another argument for sociality is based on the healed injuries in several Smilodon fossils, which would suggest that the animals needed others to provide them food.[73][74] This argument has been questioned, as cats can recover quickly from even severe bone damage and an injured Smilodon could survive if it had access to water.[75] However, a Smilodon suffering hip dysplasia at a young age that survived to adulthood suggests that it could not have survived to adulthood without aid from a social group, as this individual was unable to hunt or defend its territory due to the severity of its congenital issue.[76] The brain of Smilodon was relatively small compared to other cat species. Some researchers have argued that Smilodon's brain would have been too small for it to have been a social animal.[77] An analysis of brain size in living big cats found no correlation between brain size and sociality.[78] Another argument against Smilodon being social is that being an ambush hunter in closed habitat would likely have made group-living unnecessary, as in most modern cats.[75] Yet it has also been proposed that being the largest predator in an environment comparable to the savanna of Africa, Smilodon may have had a social structure similar to modern lions, which possibly live in groups primarily to defend optimal territory from other lions (lions are the only social big cats today).[51]

 
Tip of an S. fatalis saber imbedded in the rib of another S. fatalis

Whether Smilodon was sexually dimorphic has implications for its reproductive behavior. Based on their conclusions that Smilodon fatalis had no sexual dimorphism, Van Valkenburgh and Sacco suggested in 2002 that, if the cats were social, they would likely have lived in monogamous pairs (along with offspring) with no intense competition among males for females.[26] Likewise, Meachen-Samuels and Binder concluded in 2010 that aggression between males was less pronounced in S. fatalis than in the American lion.[27] Christiansen and Harris found in 2012 that, as S. fatalis did exhibit some sexual dimorphism, there would have been evolutionary selection for competition between males.[28] Some bones show evidence of having been bitten by other Smilodon, possibly the result of territorial battles, competition for breeding rights or over prey.[51] Two S. populator skulls from Argentina show seemingly fatal, unhealed wounds which appear to have been caused by the canines of another Smilodon (though it cannot be ruled out they were caused by kicking prey). If caused by intraspecific fighting, it may also indicate that they had social behavior which could lead to death, as seen in some modern felines (as well as indicating that the canines could penetrate bone).[79] It has been suggested that the exaggerated canines of saber-toothed cats evolved for sexual display and competition, but a statistical study of the correlation between canine and body size in S. populator found no difference in scaling between body and canine size concluded it was more likely they evolved solely for a predatory function.[80]

A set of three associated skeletons of S. fatalis found in Ecuador and described in 2021 by Reynolds, Seymour, and Evans suggests that there was prolonged parental care in Smilodon. The two subadult individuals uncovered share a unique inherited trait in their dentaries, suggesting they were siblings; a rare instance of familial relationships being found in the fossil record. The subadult specimens are also hypothesized to have been male and female, respectively, while the adult skeletal remains found at the site are believed to have belonged to their mother. The subadults were estimated to have been around two years of age at the time of their deaths, but were still growing.[81] S. fatalis had proportionally larger hyoid bones than modern felid species and thus likely produced deeper vocalizations. While Smilodon had the same number of hyoid bones as the "roaring" cats, their shape was closer to that of "purring" species.[82]

Development edit

 
Undersides of S. fatalis skulls, showing canine replacement, George C. Page Museum

Smilodon started developing its adult saber-teeth when the animal reached between 12 and 19 months of age, shortly after the completion of the eruption of the cat's baby teeth. Both baby and adult canines would be present side by side in the mouth for an approximately 11-month period, and the muscles used in making the powerful bite were developed at about one-and-a-half years old as well, eight months earlier than in a modern lion. After Smilodon reached 23 to 30 months of age, the infant teeth were shed while the adult canines grew at an average growth rate of 7 mm (0.3 in) per month during a 12-month period. They reached their full size at around 3 years of age, later than modern species of big cats. Juvenile and adolescent Smilodon specimens are extremely rare at Rancho La Brea, where the study was performed, indicating that they remained hidden or at denning sites during hunts, and depended on parental care while their canines were developing.[83][84][85]

A 2017 study indicates that juveniles were born with a robust build similar to the adults. Comparison of the bones of juvenile S. fatalis specimens from La Brea with those of the contemporaneous American lion revealed that the two cats shared a similar growth curve. Felid forelimb development during ontogeny (changes during growth) has remained tightly constrained. The curve is similar to that for modern cats such as tigers and cougars, but shifts more towards the robust direction of the axes than is seen in modern felids.[86] Examinations by Reynolds, Seymour, and Evans (2021) suggest that Smilodon had a unique and fast growth rate similar to a tiger, but that there was a prolonged period of growth in the genus similar to what is seen in lions, and that the cubs were reliant on their parents until this growth period ended.[81]

Paleopathology edit

 
Large subchondral defects in S. fatalis limb-joints (arrows)

Several Smilodon fossils show signs of ankylosing spondylitis, hyperostosis and trauma.[87] One study of 1,000 Smilodon skulls found that 36% of them had eroded parietal bones, which is where the largest jaw muscles attach. They also showed signs of microfractures, and the weakening and thinning of bones possibly caused by mechanical stress from the constant need to make stabbing motions with the canines.[88] Bony growths where the deltoid muscle inserted in the humerus is a common pathology for a La Brea specimen, which was probably due to repeated strain when Smilodon attempted to pull down prey with its forelimbs. Sternum injuries are also common, probably due to collision with prey.[89]

The frequency of trauma in S. fatalis specimens was 4.3%, compared to 2.8% in the dire wolf, which implies the ambush predatory behavior of the former led to greater risk of injury than the pursuit predatory behavior of the latter. Smilodon remains exhibit relatively more shoulder and lumbar vertebrae injuries.[90] A 2023 study documented a high degree of subchondral defects in limb-joint surfaces of S. fatalis and dire wolf specimens from the La Brea Tar pits that resembled osteochondrosis dissecans. As modern dogs with this disease are inbred, the researchers suggested this would have been the case for the prehistoric species as well as they approached extinction, but cautioned that more research was needed to determine if this was also the case in specimens from other parts of the Americas.[91]

Osteomyelitis in the left fourth metacarpal bone has been reported in a S. populator specimen dating back to Marine Isotope Stage 5. This pathology resulted in the machairodont individual becoming incapable of flexing its toe and would have severely diminished its ability to hunt prey.[92]

Distribution and habitat edit

 
Environment of what is now White Sands National Park, with S. fatalis in the reeds in the right foreground

Smilodon lived during the Pleistocene epoch (2.5 mya–10,000 years ago), and was perhaps the most recent of the saber-toothed cats.[23] It probably lived in closed habitat such as forest or bush.[93] Fossils of the genus have been found throughout the Americas.[3] The northernmost remains of the genus are S. fatalis fossils from Alberta, Canada,[94] with the southernmost remains being known from the far south of Patagonia.[95] The habitat of North America varied from subtropical forests and savannah in the south, to treeless mammoth steppes in the north. The mosaic vegetation of woods, shrubs, and grasses in southwestern North America supported large herbivores such as horses, bison, antelope, deer, camels, mammoths, mastodons, and ground sloths. North America also supported other saber-toothed cats, such as Homotherium and Xenosmilus, as well as other large carnivores including dire wolves, short-faced bear (Arctodus simus) and the American lion.[14][69][96] Competition from such carnivores may have prevented North American S. fatalis from attaining the size of South America's S. populator. The similarity in size of S. fatalis and the American lion suggests niche overlap and direct competition between these species, and they appear to have fed on similarly sized prey.[97]

 
Animals that participated in the Great American Interchange, with North American migrants like S. populator (lower right) in blue

S. gracilis entered South America during the early to middle Pleistocene, where it probably gave rise to S. populator, which lived in the eastern part of the continent. S. fatalis also entered western South America in the late Pleistocene, and the two species were thought to be divided by the Andes mountains.[8][17][23] However, in 2018, a skull of S. fatalis found in Uruguay east of the Andes was reported, which puts the idea that the two species were allopatric (geographically separated) into question.[98] The American interchange resulted in a mix of native and invasive species sharing the prairies and woodlands in South America; North American herbivores included proboscideans, horses, camelids and deer, South American herbivores included toxodonts, litopterns, ground sloths, and glyptodonts. Native metatherian predators (including the saber-toothed thylacosmilids) had gone extinct by the Pliocene, and were replaced by North American carnivores such as canids, bears, and large cats.[14]

S. populator was very successful, while Homotherium never became widespread in South America. The extinction of the thylacosmilids has been attributed to competition with Smilodon, but this is probably incorrect, as they seem to have disappeared before the arrival of the large cats. The phorusrhacid "terror birds" may have dominated the large predator niche in South America until Smilodon arrived.[14] S. populator may have been able to reach larger size than S. fatalis due to a lack of competition in Pleistocene South America; S. populator arrived after the extinction of Arctotherium angustidens, one of the largest carnivores ever, and could therefore assume the niche of mega-carnivore.[97] S. populator preferred large prey from open habitats such as grassland and plains, based on evidence gathered from isotope ratios that determined the animal's diet. In this way, the South American Smilodon species was probably similar to the modern lion. S. populator probably competed with the canid Protocyon there, but not with the jaguar, which fed primarily on smaller prey.[99][100] On the other hand, morphometry points to S. populator being best adapted for more closed environments.[101]

Extinction edit

 
Skeletons of S. fatalis (left) and the American lion, two large North American felids which went extinct during the Late Pleistocene, George C. Page Museum

Along with most of the New World Pleistocene megafauna, Smilodon became extinct by 10,000 years ago in the late Pleistocene extinction phases of North and South America. Its extinction has been linked to the decline and extinction of large herbivores. Hence, Smilodon could have been too specialized at hunting large prey and may have been unable to adapt.[56] Indeed, by the Bølling–Allerød warming event and before the Younger Dryas cooling event, S. fatalis showed changes in cranial morphology that hint towards increased specialization in larger prey and/or evolution in response to competition with other carnivores.[102] However, a 2012 study of Smilodon tooth wear found no evidence that they were limited by food resources.[103] Other explanations include climate change and competition with Homo sapiens[103] (who entered the Americas around the time Smilodon disappeared), or a combination of several factors, all of which apply to the general Late Pleistocene extinction event, rather than specifically to the extinction of the saber-toothed cats.[104] One factor often cited here is the cooling in the Younger Dryas, which may have drastically reduced the habitable space for many species. In terms of human influence, there is evidence of a fire-induced regime change in Rancho la Brea that preceded the extirpation of megafauna in the area, with humans most likely responsible for the increase in fire intensity.[105]

Writers of the first half of the twentieth century theorized that the last saber-toothed cats, Smilodon and Homotherium, became extinct through competition with the faster and more generalized felids that replaced them. It was even proposed that the saber-toothed predators were inferior to modern cats, as the ever-growing canines were thought to inhibit their owners from feeding properly. Since then, however, it has been shown that the diet of machairodontines such as Smilodon and Homotherium was diverse. They do not seem to have been limited to giant animals as prey, as suggested before, but fed on whatever was available, including bovines, equines and camelids.[106][107] Additionally, non-machairodontine felids such as the American lion and Miracinonyx also became extinct during the Late Pleistocene, and saber-toothed and conical toothed felids had formerly coexisted for more than a million years.[108] The fact that saber-teeth evolved many times in unrelated lineages also attests to the success of this feature.[104]

 
Skeletal diagram of S. populator

The youngest direct radiocarbon date for S. fatalis differs from that of S. populator by thousands of years, the former just before the Younger Dryas cooling event and the latter by the early Holocene.[109] The latest S. fatalis specimen recovered from the Rancho La Brea tar pits has been dated to 13,025 years ago.[110] A specimen of S. fatalis from Iowa dates to 13,605–13,455 years Before Present (BP).[111] The latest Smilodon populator remains found in the cave of Cueva del Medio, near the town of Soria, northeast Última Esperanza Province, Magallanes Region in southernmost Chile have been dated to 10,935–11,209 years ago.[112] The most recent credible carbon-14 date for S. fatalis has been given as 11,130 BP.[113] However, such radiocarbon dates are likely uncalibrated, meaning that they were not adjusted from calendar years to regular years. As a result, the dates appear younger than they actually are. Therefore, the S. fatalis specimen from Rancho La Brea is the youngest-recorded of the species,[109] suggesting extinction before the Younger Dryas based on its last appearance in California as opposed to other regions where megafauna declined by the Younger Dryas.[105]

See also edit

References edit

  1. ^ a b c d e Antón 2013, pp. 3–26.
  2. ^ Lund, P. W. (1842). Blik paa Brasiliens Dyreverden för sidste Jordomvæltning (in Danish). Copenhagen: Det Kongelige Danske Videnskabernes Selskabs Naturvidenskabelige og Matematiske Afhandlinger. pp. 54–57.
  3. ^ a b c d e Berta, A. (1985). (PDF). Contributions in Science, Natural History Museum of Los Angeles County. 370: 1–15. Archived from the original (PDF) on 28 May 2014.
  4. ^ a b c d e f g h i j Antón 2013, pp. 108–154.
  5. ^ Leidy, J. (1869). "The extinct mammalian fauna of Dakota and Nebraska: Including an account of some allied forms from other localities, together with a synopsis of the mammalian remains of North America". Journal of the Academy of Natural Sciences of Philadelphia. 7: 366–367. doi:10.5962/bhl.title.20910.
  6. ^ "Sabertooth". National Geographic. 21 September 2011. Retrieved 2021-10-13.
  7. ^ a b Cope, E. D. (December 1880). "On the extinct cats of America". The American Naturalist. 14 (12): 833–858. doi:10.1086/272672. JSTOR 2449549.
  8. ^ a b c d e Kurtén, B.; Werdelin, L. (1990). "Relationships between North and South American Smilodon". Journal of Vertebrate Paleontology. 10 (2): 158–169. Bibcode:1990JVPal..10..158K. doi:10.1080/02724634.1990.10011804. JSTOR 4523312.
  9. ^ Werdelin, L.; McDonald, H. G.; Shaw, C. A. (2018). Smilodon: The Iconic Sabertooth (Smilodon from South Carolina: Implications for the taxonomy of the genus ed.). Baltimore: Johns Hopkins University Press. pp. 76–95. ISBN 978-1-4214-2557-3.
  10. ^ Kurtén, B.; Anderson, E. (1980). Pleistocene Mammals of North America. New York: Columbia University Press. pp. 186–188. ISBN 978-0-231-03733-4.
  11. ^ Berta, A. (1987). "The sabercat Smilodon gracilis from Florida and a discussion of its relationships (Mammalia, Felidae, Smilodontini)". Bulletin of the Florida State Museum. 31: 1–63.
  12. ^ Churcher, C. S. (1984). "The status of Smilodontopsis (Brown, 1908) and Ischyrosmilus (Merriam, 1918): a taxonomic review of two genera of sabretooth cats (Felidae, Machairodontinae)". Royal Ontario Museum Life Sciences Contributions. 140: 14–34. doi:10.5962/bhl.title.52222. ISBN 978-0-88854-305-9.
  13. ^ Meehan, T.; Martin, L. D. J. (2003). "Extinction and re-evolution of similar adaptive types (ecomorphs) in Cenozoic North American ungulates and carnivores reflect van der Hammen's cycles". Die Naturwissenschaften. 90 (3): 131–135. Bibcode:2003NW.....90..131M. doi:10.1007/s00114-002-0392-1. PMID 12649755. S2CID 21117744.
  14. ^ a b c d e f g Antón 2013, pp. 65–76.
  15. ^ Christiansen, P. (2008). "Evolution of skull and mandible shape in cats (Carnivora: Felidae)". PLOS ONE. 3 (7): e2807. Bibcode:2008PLoSO...3.2807C. doi:10.1371/journal.pone.0002807. PMC 2475670. PMID 18665225.  
  16. ^ Paijmans, J. L. A.; Barnett, R.; Gilbert, M. T. P.; Zepeda-Mendoza, M. L.; Reumer, J. W. F.; de Vos, J.; Zazula, G.; Nagel, D.; Baryshnikov, G. F.; Leonard, J. A.; Rohland, N.; Westbury, M. V.; Barlow, A.; Hofreiter, M. (2017-10-19). "Evolutionary History of Saber-Toothed Cats Based on Ancient Mitogenomics". Current Biology. 27 (21): 3330–3336.e5. Bibcode:2017CBio...27E3330P. doi:10.1016/j.cub.2017.09.033. PMID 29056454.
  17. ^ a b c Rincón, A.; Prevosti, F.; Parra, G. (2011). "New saber-toothed cat records (Felidae: Machairodontinae) for the Pleistocene of Venezuela, and the Great American Biotic Interchange". Journal of Vertebrate Paleontology. 31 (2): 468–478. Bibcode:2011JVPal..31..468R. doi:10.1080/02724634.2011.550366. hdl:11336/69016. JSTOR 25835839. S2CID 129693331.
  18. ^ de Castro, Mariela Cordeiro; Langer, Max Cardoso (2008). "New postcranial remains of Smilodon populator Lund, 1842 from South-Central Brazil". Revista Brasileira de Paleontologia. 11 (3): 199–206. doi:10.4072/rbp.2008.3.06.
  19. ^ "What Is a Sabertooth?". University of California Museum of Paleontology. December 2005. Retrieved 2012-06-12.
  20. ^ Janczewski, D. N.; Yuhki, N.; Gilbert, D. A.; Jefferson, G. T.; O'Brien, S. J. (1992). "Molecular phylogenetic inference from saber-toothed cat fossils of Rancho La Brea". Proceedings of the National Academy of Sciences. 89 (20): 9769–9773. Bibcode:1992PNAS...89.9769J. doi:10.1073/pnas.89.20.9769. PMC 50214. PMID 1409696.
  21. ^ Barnett, R.; Barnes, I.; Phillips, M. J.; Martin, L. D.; Harington, C. R.; Leonard, J. A.; Cooper, A. (2005). "Evolution of the extinct sabretooths and the American cheetah-like cat". Current Biology. 15 (15): R589–R590. Bibcode:2005CBio...15.R589B. doi:10.1016/j.cub.2005.07.052. PMID 16085477. S2CID 17665121.
  22. ^ van den Hoek Ostende, L. W.; Morlo, M.; Nagel, D. (2006). "Majestic killers: the sabre-toothed cats (Fossils explained 52)". Geology Today. 22 (4): 150–157. doi:10.1111/j.1365-2451.2006.00572.x. S2CID 128960196.
  23. ^ a b c d e f g Turner, A.; Antón, M. (1997). The Big Cats and Their Fossil Relatives: An Illustrated Guide to Their Evolution and Natural History. Columbia University Press. pp. 57–58, 67–68. ISBN 978-0-231-10229-2. OCLC 34283113.
  24. ^ "What Is a Sabertooth?". University of California Museum of Paleontology. Retrieved 2013-04-08.
  25. ^ Slater, G. J.; Valkenburgh, B. V. (2008). "Long in the tooth: evolution of sabertooth cat cranial shape". Paleobiology. 34 (3): 403–419. Bibcode:2008Pbio...34..403S. doi:10.1666/07061.1. ISSN 0094-8373. S2CID 85353590.
  26. ^ a b Van Valkenburgh, B.; Sacco, T. (2002). "Sexual dimorphism, social behavior and intrasexual competition in large Pleistocene carnivorans". Journal of Vertebrate Paleontology. 22 (1): 164–169. doi:10.1671/0272-4634(2002)022[0164:sdsbai]2.0.co;2. JSTOR 4524203. S2CID 86156959.
  27. ^ a b Meachen-Samuels, J.; Binder, W. (2010). "Sexual dimorphism and ontogenetic growth in the American lion and sabertoothed cat from Rancho La Brea". Journal of Zoology. 280 (3): 271–279. doi:10.1111/j.1469-7998.2009.00659.x.
  28. ^ a b Christiansen, Per; Harris, John M. (2012). "Variation in Craniomandibular Morphology and Sexual Dimorphism in Pantherines and the Sabercat Smilodon fatalis". PLOS ONE. 7 (10): e48352. Bibcode:2012PLoSO...748352C. doi:10.1371/journal.pone.0048352. PMC 3482211. PMID 23110232.
  29. ^ a b c Christiansen, Per; Harris, John M. (2005). "Body size of Smilodon (Mammalia: Felidae)". Journal of Morphology. 266 (3): 369–84. doi:10.1002/jmor.10384. PMID 16235255. S2CID 27233870.
  30. ^ . San Diego Zoo Global. January 2009. Archived from the original on 2013-02-03. Retrieved 2013-05-07.
  31. ^ Sorkin, B. (2008). "A biomechanical constraint on body mass in terrestrial mammalian predators". Lethaia. 41 (4): 333–347. Bibcode:2008Letha..41..333S. doi:10.1111/j.1502-3931.2007.00091.x.
  32. ^ Manzuetti, A.; Perea, D.; Jones, W.; Ubilla, M.; Rinderknecht, A. (2020). "An extremely large saber-tooth cat skull from Uruguay (late Pleistocene–early Holocene, Dolores Formation): body size and paleobiological implications". Alcheringa: An Australasian Journal of Palaeontology. 44 (2): 332–339. Bibcode:2020Alch...44..332M. doi:10.1080/03115518.2019.1701080. S2CID 216505747.
  33. ^ "Hallazgo inédito en Miramar: huellas fosilizadas de un gran tigre dientes de sable". 0223.com.ar (in Spanish). 0223. May 26, 2016. Retrieved 28 May 2016.
  34. ^ Perkins, Sid (June 10, 2016). "First fossil footprints of saber-toothed cats are bigger than Bengal tiger paws". Science. doi:10.1126/science.aag0602.
  35. ^ a b c d Antón 2013, pp. 157–176.
  36. ^ Allen, W. L.; Cuthill, I. C.; Scott-Samuel, N. E.; Baddeley, R. (2010). "Why the leopard got its spots: relating pattern development to ecology in felids". Proceedings of the Royal Society B. 278 (1710): 1373–1380. doi:10.1098/rspb.2010.1734. PMC 3061134. PMID 20961899.
  37. ^ Miller, G. J. (1969). "A new hypothesis to explain the method of food ingestion used by Smilodon californicus Bovard". Tebiwa. 12: 9–19.
  38. ^ a b c Antón, M.; García-Perea, R.; Turner, A. (1998). "Reconstructed facial appearance of the sabretoothed felid Smilodon". Zoological Journal of the Linnean Society. 124 (4): 369–386. doi:10.1111/j.1096-3642.1998.tb00582.x.
  39. ^ Antón, Mauricio; Siliceo, Gema; Pastor, Juan F.; Salesa, Manuel J. (2022). "Concealed weapons: A revised reconstruction of the facial anatomy and life appearance of the sabre-toothed cat Homotherium latidens (Felidae, Machairodontinae)". Quaternary Science Reviews. 284: 107471. Bibcode:2022QSRv..28407471A. doi:10.1016/j.quascirev.2022.107471. hdl:10261/270770. S2CID 248168629.
  40. ^ a b Coltrain, J. B.; Harris, J. M.; Cerling, T. E.; Ehleringer, J. R.; Dearing, M.-D.; Ward, J.; Allen, J. (2004). (PDF). Palaeogeography, Palaeoclimatology, Palaeoecology. 205 (3–4): 199–219. Bibcode:2004PPP...205..199C. doi:10.1016/j.palaeo.2003.12.008. Archived from the original (PDF) on November 11, 2011.
  41. ^ Antón 2013, pp. 203–204.
  42. ^ Feranec, R. S. (2005). "Growth rate and duration of growth in the adult canine of S. gracilis and inferences on diet through stable isotope analysis" (PDF). Bulletin of the Florida Museum of Natural History. 45 (4): 369–377. doi:10.58782/flmnh.psyo5090 – via University of Florida.
  43. ^ Feranec, Robert S.; DeSantis, Larisa R. G. (Summer 2014). "Understanding specifics in generalist diets of carnivorans by analyzing stable carbon isotope values in Pleistocene mammals of Florida". Paleobiology. 40 (3): 477–493. Bibcode:2014Pbio...40..477F. doi:10.1666/13055. ISSN 0094-8373. Retrieved 21 January 2024 – via Cambridge Core.
  44. ^ DeSantis, Larisa R. G.; Crites, Jonathan M.; Feranec, Robert S.; Fox-Dobbs, Kena; Farrell, Aisling B.; Harris, John M.; Takeuchi, Gary T.; Cerling, Thure E. (2019). "Causes and Consequences of Pleistocene Megafaunal Extinctions as Revealed from Rancho La Brea Mammals". Current Biology. 29 (15): 2488–2495. Bibcode:2019CBio...29E2488D. doi:10.1016/j.cub.2019.06.059. PMID 31386836.
  45. ^ Vanvalkenburgh, B.; Hertel, F. (1993). "Tough Times at La Brea: Tooth Breakage in Large Carnivores of the Late Pleistocene". Science. 261 (5120): 456–459. Bibcode:1993Sci...261..456V. doi:10.1126/science.261.5120.456. PMID 17770024. S2CID 39657617.
  46. ^ Dantas, Mário André Trindade; Cherkinsky, Alexander; Lessa, Carlos Micael Bonfim; Santos, Luciano Vilaboim; Cozzuol, Mario Alberto; Omena, Érica Cavalcante; Silva, Jorge Luiz Lopes; Sial, Alcides Nóbrega; Bocherens, Hervé (2020-07-14). "Isotopic paleoecology (δ13C, δ18O) of a late Pleistocene vertebrate community from the Brazilian Intertropical Region". Revista Brasileira de Paleontologia. 23 (2): 138–152. doi:10.4072/rbp.2020.2.05. ISSN 2236-1715.
  47. ^ Van Valkenburgh, B.; Teaford, M. F.; Walker, A. (1990). "Molar microwear and diet in large carnivores: inferences concerning diet in the sabretooth cat, Smilodon fatalis". Journal of Zoology. 222 (2): 319–340. doi:10.1111/j.1469-7998.1990.tb05680.x.
  48. ^ Moreno Rodríguez, Ana P.; Chimento, Nicolás R.; Agnolín, Federico L.; Jofré, Guillermo; Gentil, Adriel (2022). "A possible Smilodon (Mammalia, Felidae) Coprolite from the Pleistocene of Argentina". PALAIOS. 37 (7): 402–410. Bibcode:2022Palai..37..402M. doi:10.2110/palo.2021.056. ISSN 1938-5323. S2CID 251078622.
  49. ^ DeSantis, Larisa R.G.; Shaw, Christopher A. (2018). "Sabertooth Cats with Toothaches: Impacts of Dental Injuries on Feeding Behavior in Late Pleistocene Smilodon Fatalis (Mammalia, Felidae) from Rancho la Brea (Los Angeles, California)". Geological Society of America Abstracts with Programs. 50 (6): 322567. doi:10.1130/abs/2018AM-322567.
  50. ^ Van Valkenburgh, B. (1991). "Iterative evolution of hypercarnivory in canids (Mammalia: Carnivora): evolutionary interactions among sympatric predators". Paleobiology. 17 (4): 340–362. Bibcode:1991Pbio...17..340V. doi:10.1017/S0094837300010691. JSTOR 2400749. S2CID 251052044.
  51. ^ a b c d e Antón 2013, pp. 176–216.
  52. ^ Gonyea, W. J. (1976). "Behavioral implications of saber-toothed felid morphology". Paleobiology. 2 (4): 332–342. Bibcode:1976Pbio....2..332G. doi:10.1017/S0094837300004966. JSTOR 2400172. S2CID 87481727.
  53. ^ "What Is a Sabertooth?". Berkeley.edu. Retrieved 1 June 2017.
  54. ^ a b Anton, Mauricio (2013). Sabertooth.
  55. ^ Agnolin, F. L.; Chimento, N. R.; Campo, D. H.; Magnussen, M.; Boh, D.; De Cianni, F. (2019). "Large Carnivore Footprints from the Late Pleistocene of Argentina". Ichnos. 26 (2): 119–126. Bibcode:2019Ichno..26..119A. doi:10.1080/10420940.2018.1479962. S2CID 134190731.
  56. ^ a b c d Meachen-Samuels, J. A.; Van Valkenburgh, B. (2010). "Radiographs reveal exceptional forelimb strength in the sabertooth cat, Smilodon fatalis". PLOS ONE. 5 (7): e11412. Bibcode:2010PLoSO...511412M. doi:10.1371/journal.pone.0011412. ISSN 1932-6203. PMC 2896400. PMID 20625398.  
  57. ^ McHenry, C. R.; Wroe, S.; Clausen, P. D.; Moreno, K.; Cunningham, E. (2007). "Supermodeled sabercat, predatory behavior in Smilodon fatalis revealed by high-resolution 3D computer simulation". PNAS. 104 (41): 16010–16015. Bibcode:2007PNAS..10416010M. doi:10.1073/pnas.0706086104. PMC 2042153. PMID 17911253.
  58. ^ Anyonge, W. (1996). "Microwear on canines and killing behavior in large carnivores: saber function in Smilodon fatalis". Journal of Mammalogy. 77 (4): 1059–1067. doi:10.2307/1382786. JSTOR 1382786.
  59. ^ Figueirido, B.; Lautenschlager, S.; Pérez-Ramos, A.; Van Valkenburgh, B. (2018). "Distinct Predatory Behaviors in Scimitar- and Dirk-Toothed Sabertooth Cats". Current Biology. 28 (20): 3260–3266.e3. Bibcode:2018CBio...28E3260F. doi:10.1016/j.cub.2018.08.012. hdl:10630/29727. PMID 30293717.
  60. ^ Brown, J. G. (2014). "Jaw function in Smilodon fatalis: a reevaluation of the canine shear-bite and a proposal for a new forelimb-powered class 1 lever model". PLOS ONE. 9 (10): e107456. Bibcode:2014PLoSO...9j7456B. doi:10.1371/journal.pone.0107456. ISSN 1932-6203. PMC 4182664. PMID 25272032.  
  61. ^ Domínguez-Rodrigo, Manuel; Egeland, Charles P.; Cobo-Sánchez, Lucía; Baquedano, Enrique; Hulbert, Richard C. (2022). "Sabertooth carcass consumption behavior and the dynamics of Pleistocene large carnivoran guilds". Scientific Reports. 12 (1): 6045. Bibcode:2022NatSR..12.6045D. doi:10.1038/s41598-022-09480-7. PMC 9061710. PMID 35501323.
  62. ^ Hecht, J. (1 October 2007). "Sabre-tooth cat had a surprisingly delicate bite". New Scientist.
  63. ^ Wroe, S.; McHenry2, C.; Thomason, J. (2004). (PDF). Proceedings of the Royal Society. 272 (1563): 619–25. doi:10.1098/rspb.2004.2986. PMC 1564077. PMID 15817436. Archived from the original (PDF) on 2013-08-25.{{cite journal}}: CS1 maint: numeric names: authors list (link)
  64. ^ Christiansen, P. (2007). "Comparative bite forces and canine bending strength in feline and sabretooth felids: implications for predatory ecology". Zoological Journal of the Linnean Society. 151 (2): 423–437. doi:10.1111/j.1096-3642.2007.00321.x.
  65. ^ Andersson, K.; Norman, D.; Werdelin, L. (2011). "Sabretoothed carnivores and the killing of large prey". PLOS ONE. 6 (10): e24971. Bibcode:2011PLoSO...624971A. doi:10.1371/journal.pone.0024971. PMC 3198467. PMID 22039403.  
  66. ^ Martin, L. D. (1980). "Functional morphology and the evolution of cats". Transactions of the Nebraska Academy of Sciences. 8: 141–154.
  67. ^ Figueirido, B.; Lautenschlager, S.; Pérez-Ramos, A.; Van Valkenburgh, B. (2018). "Distinct Predatory Behaviors in Scimitar- and Dirk-Toothed Sabertooth Cats". Current Biology. 28 (20): 3260–3266.e3. Bibcode:2018CBio...28E3260F. doi:10.1016/j.cub.2018.08.012. hdl:10630/29727. PMID 30293717.
  68. ^ Shaw, Christopher A.; Quinn, James P. (September 15, 2015). John M. Harris (ed.). (PDF). Science Series 42: Contributions in Science (A special volume entitled La Brea and Beyond: the Paleontology of Asphalt–Preserved Biotas in commemoration of the 100th anniversary of the Natural History Museum of Los Angeles County's excavations at Rancho La Brea). Natural History Museum of Los Angeles County: 91–95. Archived from the original (PDF) on December 25, 2016. Retrieved September 30, 2017.
  69. ^ a b c Antón 2013, pp. 30–33.
  70. ^ Carbone, C.; Maddox, T.; Funston, P. J.; Mills, M. G. L.; Grether, G. F.; Van Valkenburgh, B. (2009). "Parallels between playbacks and Pleistocene tar seeps suggest sociality in an extinct sabretooth cat, Smilodon". Biology Letters. 5 (1): 81–85. doi:10.1098/rsbl.2008.0526. PMC 2657756. PMID 18957359.
  71. ^ Kiffner, C. (2009). "Coincidence or evidence: was the sabretooth cat Smilodon social?". Biology Letters. 5 (4): 561–562. doi:10.1098/rsbl.2009.0008. PMC 2781900. PMID 19443504.
  72. ^ Van Valkenburgh, B.; Maddox, T.; Funston, P. J.; Mills, M. G. L.; Grether, G. F.; Carbone, C. (2009). "Sociality in Rancho La Brea Smilodon: arguments favour 'evidence' over 'coincidence'". Biology Letters. 5 (4): 563–564. doi:10.1098/rsbl.2009.0261. PMC 2781931.
  73. ^ Heald, F. (1989). ""Injuries and diseases in Smilodon californicus Bovard, 1904, (Mammalia, Felidae) from Rancho La Brea, California". Journal of Vertebrate Paleontology. 9 (3): 24A.
  74. ^ Balisi, M. A.; Sharma, A. K.; Howard, C. M.; Shaw, C. A.; Klapper, R.; Lindsey, Emily L. (2020). "Computed tomography reveals hip dysplasia in Smilodon: Implications for social behavior in an extinct Pleistocene predator". bioRxiv 10.1101/2020.01.07.897348.
  75. ^ a b McCall, S.; Naples, V.; Martin, L. (2003). "Assessing behavior in extinct animals: was Smilodon social?". Brain, Behavior and Evolution. 61 (3): 159–164. doi:10.1159/000069752. PMID 12697957. S2CID 2756104.
  76. ^ Balisi, Mairin A.; Sharma, Abhinav K.; Howard, Carrie M.; Shaw, Christopher A.; Klapper, Robert; Lindsey, Emily L. (2021). "Computed tomography reveals hip dysplasia in the extinct Pleistocene saber-tooth cat Smilodon". bioRxiv. 11 (1): 21271. doi:10.1101/2020.01.07.897348. PMC 8553773. PMID 34711910. S2CID 235663241.
  77. ^ Radinsky, L. B. (1975). "Evolution of the felid brain". Brain, Behavior and Evolution. 11 (3–4): 214–254. doi:10.1159/000123636. PMID 1181005.
  78. ^ Yamaguchi, N.; Kitchener, A. C.; Gilissen, E.; MacDonald, D. W. (2009). "Brain size of the lion (Panthera leo) and the tiger (P. tigris): implications for intrageneric phylogeny, intraspecific differences and the effects of captivity". Biological Journal of the Linnean Society. 98 (1): 85–93. doi:10.1111/j.1095-8312.2009.01249.x.
  79. ^ Chimento, N. R.; Agnolin, F. L.; Soibelzon, L.; Ochoa, J. G.; Buide, V. (2019). "Evidence of intraspecific agonistic interactions in Smilodon populator (Carnivora, Felidae)". Comptes Rendus Palevol. 18 (4): 449–454. Bibcode:2019CRPal..18..449C. doi:10.1016/j.crpv.2019.02.006.
  80. ^ O’Brien, D. M (2019). "Static scaling and the evolution of extreme canine size in a saber-toothed cat (Smilodon fatalis)". Integrative and Comparative Biology. 59 (5): 1303–1311. doi:10.1093/icb/icz054. PMID 31120517.
  81. ^ a b Reynolds, Ashley R.; Seymour, Kevin L.; Evans, David C. (January 7, 2021). "Smilodon fatalis siblings reveal life history in a saber-toothed cat". iScience. 24 (1): 101916. Bibcode:2021iSci...24j1916R. doi:10.1016/j.isci.2020.101916. PMC 7835254. PMID 33532710.
  82. ^ Deutsch, A. R.; Langerhans, R. B.; Flores, D; Hartstone-Rose, A (2023). "The roar of Rancho La Brea? Comparative anatomy of modern and fossil felid hyoid bones". Journal of Morphology. 284 (10): e21627. doi:10.1002/jmor.21627. PMID 37708512. S2CID 261090355.
  83. ^ . ScienceDaily. 2015-07-01. Archived from the original on 2015-07-02. Retrieved 2015-07-02.
  84. ^ Mihlbachler, M. C.; Wysocki, M. A.; Feranec, R. S.; Tseng, Z. J.; Bjornsson, C. S. (2015-07-01). "Using a novel absolute ontogenetic age determination technique to calculate the timing of tooth eruption in the saber-toothed cat, Smilodon fatalis". PLOS ONE. 10 (7): e0129847. Bibcode:2015PLoSO..1029847W. doi:10.1371/journal.pone.0129847. PMC 4489498. PMID 26132165.  
  85. ^ Feranec, R. C. (2004). "Isotopic evidence of saber-tooth development, growth rate, and diet from the adult canine of Smilodon fatalis from Rancho La Brea". Palaeogeography, Palaeoclimatology, Palaeoecology. 206 (3–4): 303–310. Bibcode:2004PPP...206..303F. doi:10.1016/j.palaeo.2004.01.009.
  86. ^ Long, K.; Prothero, D.; Madan, M.; Syverson, V. J. P.; Smith, T. (2017). "Did saber-tooth kittens grow up musclebound? A study of postnatal limb bone allometry in felids from the Pleistocene of Rancho La Brea". PLOS ONE. 12 (9): e0183175. Bibcode:2017PLoSO..1283175L. doi:10.1371/journal.pone.0183175. PMC 5617143. PMID 28953899.
  87. ^ Bjorkengren, A. G.; Sartoris, D. J.; Shermis, S.; Resnick, D. (1987). "Patterns of paravertebral ossification in the prehistoric saber-toothed cat". American Journal of Roentgenology. 148 (4): 779–782. doi:10.2214/ajr.148.4.779. PMID 3103404.
  88. ^ Duckler, G. L. (1997). "Parietal depressions in skulls of the extinct saber-toothed felid Smilodon fatalis: evidence of mechanical strain". Journal of Vertebrate Paleontology. 17 (3): 600–609. Bibcode:1997JVPal..17..600D. doi:10.1080/02724634.1997.10011006.
  89. ^ Antón 2013, p. 199.
  90. ^ Brown, C.; Balisi, M.; Shaw, C. A.; Van Valkenburgh, B. (2017). "Skeletal trauma reflects hunting behaviour in extinct sabre-tooth cats and dire wolves". Nature Ecology & Evolution. 1 (5): 0131. Bibcode:2017NatEE...1..131B. doi:10.1038/s41559-017-0131. PMID 28812696. S2CID 8008808.
  91. ^ Schmökel, Hugo; Farrell, Aisling; Balisi, Mairin F. (2023). "Subchondral defects resembling osteochondrosis dissecans in joint surfaces of the extinct saber-toothed cat Smilodon fatalis and dire wolf Aenocyon dirus". PLOS ONE. 18 (7): e0287656. Bibcode:2023PLoSO..1887656S. doi:10.1371/journal.pone.0287656. PMC 10337945. PMID 37436967.
  92. ^ Luna, Carlos A.; Pool, Roy R.; Ercoli, Marcos D.; Chimento, Nicolás R.; Barbosa, Fernando H. de S.; Zurita, Alfredo E.; Cuaranta, Pedro (22 May 2023). "Osteomyelitis in the manus of Smilodon populator (Felidae, Machairodontinae) from the Late Pleistocene of South America". Palaeoworld. doi:10.1016/j.palwor.2023.05.001. ISSN 1871-174X. Retrieved 5 February 2024 – via Elsevier Science Direct.
  93. ^ Meloro, C.; Elton, S.; Louys, J.; Bishop, L. C.; Ditchfield, P. (2013). "Cats in the forest: predicting habitat adaptations from humerus morphometry in extant and fossil Felidae (Carnivora)" (PDF). Paleobiology. 39 (3): 323–344. Bibcode:2013Pbio...39..323M. doi:10.1666/12001. S2CID 83957027.
  94. ^ Reynolds, A. R.; Seymour, K. L.; Evans, D. C. (2019). "Late Pleistocene records of felids from Medicine Hat, Alberta, including the first Canadian record of the sabre-toothed cat Smilodon fatalis". Canadian Journal of Earth Sciences. 56 (10): 1052–1060. Bibcode:2019CaJES..56.1052R. doi:10.1139/cjes-2018-0272. hdl:1807/96725. S2CID 134586651.
  95. ^ Villavicencio, Natalia A.; Lindsey, Emily L.; Martin, Fabiana M.; Borrero, Luis A.; Moreno, Patricio I.; Marshall, Charles R.; Barnosky, Anthony D. (February 2016). "Combination of humans, climate, and vegetation change triggered Late Quaternary megafauna extinction in the Última Esperanza region, southern Patagonia, Chile". Ecography. 39 (2): 125–140. Bibcode:2016Ecogr..39..125V. doi:10.1111/ecog.01606. ISSN 0906-7590.
  96. ^ DeSantis, L.R.G.; Schubert, B.W.; Schmitt-Linville, E.; Ungar, P.; Donohue, S.; Haupt, R.J. (September 15, 2015). John M. Harris (ed.). (PDF). Science Series 42: Contributions in Science (A special volume entitled La Brea and Beyond: the Paleontology of Asphalt–Preserved Biotas in commemoration of the 100th anniversary of the Natural History Museum of Los Angeles County's excavations at Rancho La Brea). Natural History Museum of Los Angeles County: 37–52. Archived from the original (PDF) on December 20, 2016. Retrieved February 6, 2017.
  97. ^ a b Sherani, S. (2016). A new specimen-dependent method of estimating felid body mass (No. e2327v2). PeerJ Preprints.
  98. ^ Manzuetti, A.; Perea, D.; Ubilla, M.; Rinderknecht, A. (2018). "First record of Smilodon fatalis Leidy, 1868 (Felidae, Machairodontinae) in the extra-Andean region of South America (late Pleistocene, Sopas Formation), Uruguay: Taxonomic and paleobiogeographic implications". Quaternary Science Reviews. 180: 57–62. Bibcode:2018QSRv..180...57M. doi:10.1016/j.quascirev.2017.11.024.
  99. ^ Bocherens, H.; Cotte, M.; Bonini, R.; Scian, D.; Straccia, P.; Soibelzon, L.; Prevosti, F. J. (2016-04-24). "Paleobiology of sabretooth cat Smilodon population in the Pampean Region (Buenos Aires Province, Argentina) around the Last Glacial Maximum: Insights from carbon and nitrogen stable isotopes in bone collagen". Palaeogeography, Palaeoclimatology, Palaeoecology. 449: 463–474. Bibcode:2016PPP...449..463B. doi:10.1016/j.palaeo.2016.02.017.
  100. ^ Hays, B. (2016-03-21). "Saber-toothed cats were the lions of prehistoric South America". UPI Science News. UPI. Retrieved 19 April 2016.
  101. ^ Meloro, Carlo; Elton, Sarah; Louys, Julien; Bishop, Laura C.; Ditchfield, Peter (18 March 2013). "Cats in the forest: predicting habitat adaptations from humerus morphometry in extant and fossil Felidae (Carnivora)". Paleobiology. 39 (3): 323–344. Bibcode:2013Pbio...39..323M. doi:10.1666/12001. ISSN 0094-8373. Retrieved 21 January 2024 – via Cambridge Core.
  102. ^ Meachen, Julie A.; O'Keefe, F. Robin; Sadleir, Rudyard W. (2014). "Evolution in the sabre-tooth cat, Smilodon fatalis, in response to Pleistocene climate change". Journal of Evolutionary Biology. 27 (4): 714–723. doi:10.1111/jeb.12340. PMID 24779050.
  103. ^ a b DeSantis, L. R. G.; Schubert, B. W.; Scott, J. R.; Ungar, P. S. (2012). "Implications of diet for the extinction of saber-toothed cats and American lions". PLOS ONE. 7 (12): e52453. Bibcode:2012PLoSO...752453D. doi:10.1371/journal.pone.0052453. PMC 3530457. PMID 23300674.  
  104. ^ a b Antón 2013, pp. 217–230.
  105. ^ a b O'Keefe, F. Robin; Dunn, Regan E.; Weitzel, Elic M.; Waters, Michael R.; Martinez, Lisa N.; Binder, Wendy J.; Southon, John R.; Cohen, Joshua E.; Meachen, Julie A.; DeSantis, Larisa R. G.; Kirby, Matthew E.; Ghezzo, Elena; Coltrain, Joan B.; Fuller, Benjamin T.; Farrell, Aisling B.; Takuechi, Gary T.; MacDonald, Glen; Davis, Edward B.; Lindsey, Emily L. (2023). "Pre–Younger Dryas megafaunal extirpation at Rancho La Brea linked to fire-driven state shift". Science. 381 (6659): eabo3594. doi:10.1126/science.abo3594. PMID 37590347.
  106. ^ Bocherens, Hervé (2015-06-01). "Isotopic tracking of large carnivore palaeoecology in the mammoth steppe". Quaternary Science Reviews. 117: 42–71. Bibcode:2015QSRv..117...42B. doi:10.1016/j.quascirev.2015.03.018. ISSN 0277-3791.
  107. ^ Prevosti, Francisco J.; Martin, Fabiana M. (2013-08-14). "Paleoecology of the mammalian predator guild of Southern Patagonia during the latest Pleistocene: Ecomorphology, stable isotopes, and taphonomy". Quaternary International. Ranked habitats and the process of human colonization of South America. 305: 74–84. Bibcode:2013QuInt.305...74P. doi:10.1016/j.quaint.2012.12.039. hdl:11336/84524. ISSN 1040-6182.
  108. ^ Antón 2013, p. 223.
  109. ^ a b Stuart, Anthony J. (August 20, 2022). "Chapter 6. North America: mastodon, ground sloths, and sabertooth cats". Vanished Giants: The Lost World of the Ice Age. University of Chicago Press. pp. 67–112. ISBN 978-0-226-82403-1.
  110. ^ O'Keefe, F.R.; Fet, E.V.; Harris, J.M. (2009). "Compilation, calibration, and synthesis of faunal and floral radiocarbon dates, Rancho La Brea, California". Contributions in Science. 518: 1–16. doi:10.5962/p.226783. S2CID 128107590.
  111. ^ Hill, Matthew G.; Easterla, David A. (May 2023). "A complete sabertooth cat cranium from the Midcontinent of North America and its evolutionary and ecological context". Quaternary Science Reviews. 307: 108045. Bibcode:2023QSRv..30708045H. doi:10.1016/j.quascirev.2023.108045. S2CID 257861663.
  112. ^ Prieto, Alfredo; Labarca, Rafael; Sierpe, Víctor (2010). "New evidence of the sabertooth cat Smilodon (Carnivora: Machairodontinae) in the late Pleistocene of southern Chilean Patagonia". Revista Chilena de Historia Natural. 83 (2). doi:10.4067/S0716-078X2010000200010.
  113. ^ Fiedel, Stuart (2009). "Sudden Deaths: The Chronology of Terminal Pleistocene Megafaunal Extinction" (PDF). In Haynes, Gary (ed.). American Megafaunal Extinctions at the End of the Pleistocene. Vertebrate Paleobiology and Paleoanthropology. Springer. pp. 21–37. doi:10.1007/978-1-4020-8793-6_2. ISBN 978-1-4020-8792-9.

Bibliography edit

smilodon, extinct, genus, archosaurian, reptile, originally, named, zanclodon, genus, felids, belonging, extinct, subfamily, machairodontinae, best, known, saber, toothed, predators, prehistoric, mammals, although, commonly, known, saber, toothed, tiger, close. For the extinct genus of archosaurian reptile originally named Smilodon see Zanclodon Smilodon is a genus of felids belonging to the extinct subfamily Machairodontinae It is one of the best known saber toothed predators and prehistoric mammals Although commonly known as the saber toothed tiger it was not closely related to the tiger or other modern cats Smilodon lived in the Americas during the Pleistocene epoch 2 5 mya 10 000 years ago The genus was named in 1842 based on fossils from Brazil the generic name means scalpel or two edged knife combined with tooth Three species are recognized today S gracilis S fatalis and S populator The two latter species were probably descended from S gracilis which itself probably evolved from Megantereon The hundreds of specimens obtained from the La Brea Tar Pits in Los Angeles constitute the largest collection of Smilodon fossils SmilodonTemporal range Early Pleistocene to Early Holocene 2 5 0 01 Ma PreꞒ Ꞓ O S D C P T J K Pg N Mounted S populator skeleton at Tellus Science MuseumScientific classificationDomain EukaryotaKingdom AnimaliaPhylum ChordataClass MammaliaOrder CarnivoraSuborder FeliformiaFamily FelidaeSubfamily MachairodontinaeTribe SmilodontiniGenus SmilodonLund 1842Type species Smilodon populatorLund 1842Other species S fatalis Leidy 1869 S gracilis Cope 1880SynonymsGenus synonymy Munifelis Munis 1845Trucifelis Leidy 1868Smilodontopsis Brown 1908Prosmilodon Rusconi 1929Smilodontidion Kraglievich 1948 Species synonymy S populator Munifelis bonaerensis Munis 1845Smilodon blainvillii Desmarest 1860Machaerodus bonaerensis Burmeister 1867Machaerodus necator Gervais 1878Smilodon ensenadensis Ameghino 1888Machaerodus ensenadensis Ameghino 1889Smilodon crucians Ameghino 1904Smilodon bonaerensis Ameghino 1907Smilodon neogaeus ensenadensis Boule amp Thevenin 1920Smilodon Prosmilodon ensenadensis Rusconi 1929Smilodon neogaeus de Paula Couto 1940Smilodon necator de Paula Couto 1940Smilodon Prosmilodon ensenadensis ferox Kraglievich 1947Smilodon Prosmilodon ensenadensis minor Kraglievich 1948Smilodontidion riggii Kraglievich 1948Machaerodus neogaeus Pictet 1953Felis smilodon Desmarest 1953Smilodon populator populator de Paula Couto 1955S fatalis Felis Trucifelis fatalis Leidy 1868Trucifelis fatalis Leidy 1869Machaerodus fatalis Lydekker 1884Drepanodon floridanus Leidy 1889Machaerodus floridanus Leidy 1889Uncia mercerii Cope 1895Smilodon floridanus Adams 1896Machaerodus Smilodon mercerii Cope 1899Smilodon californicus Bovard 1907Smilodontopsis troglodytes Brown 1908Smilodontopsis conardi Brown 1908Smilodontopsis mercerii Brown 1908Smilodon nebraskensis Matthew 1918Machaerodus mercerii Matthew 1918Smilodon Trucifelis californicus Merriam amp Stock 1932Smilodon Trucifelis fatalis Merriam amp Stock 1932Smilodon Trucifelis nebraskensis Merriam amp Stock 1932Smilodon Trucifelis californicus brevipes Merriam amp Stock 1932Smilodon trinitensis Slaughter 1960S gracilis Machaerodus Smilodon gracilis Cope 1899Smilodon Smilodontopsis gracilis Merriam amp Stock 1932Megantereon gracilis Broom amp Schepers 1946Ischyrosmilus gracilis Churcher 1984Smilodontopsis gracilis Berta 1995Overall Smilodon was more robustly built than any extant cat with particularly well developed forelimbs and exceptionally long upper canine teeth Its jaw had a bigger gape than that of modern cats and its upper canines were slender and fragile being adapted for precision killing S gracilis was the smallest species at 55 to 100 kg 120 to 220 lb in weight S fatalis had a weight of 160 to 280 kg 350 to 620 lb and height of 100 cm 39 in Both of these species are mainly known from North America but remains from South America have also been attributed to them S populator from South America was the largest species at 220 to 436 kg 485 to 961 lb in weight and 120 cm 47 in in height and was among the largest known felids The coat pattern of Smilodon is unknown but it has been artistically restored with plain or spotted patterns In North America Smilodon hunted large herbivores such as bison and camels and it remained successful even when encountering new prey species in South America Smilodon is thought to have killed its prey by holding it still with its forelimbs and biting it but it is unclear in what manner the bite itself was delivered Scientists debate whether Smilodon had a social or a solitary lifestyle analysis of modern predator behavior as well as of Smilodon s fossil remains could be construed to lend support to either view Smilodon probably lived in closed habitats such as forests and bush which would have provided cover for ambushing prey Smilodon died out at the same time that most North and South American megafauna disappeared about 10 000 years ago Its reliance on large animals has been proposed as the cause of its extinction S fatalis may have been impacted by habitat turnover and loss of prey it specialized on due to possible climatic plus anthropogenic impacts and other factors while the extinction of S populator remains poorly understood Contents 1 Taxonomy 1 1 Evolution 2 Description 2 1 Skeleton 2 2 External features 3 Paleobiology 3 1 Diet 3 2 Predatory behavior 3 3 Natural traps 3 4 Social life 3 5 Development 3 6 Paleopathology 4 Distribution and habitat 5 Extinction 6 See also 7 References 8 BibliographyTaxonomy edit nbsp S populator skull and syntype canine from Lund s collection Zoological Museum CopenhagenDuring the 1830s Danish naturalist Peter Wilhelm Lund and his assistants collected fossils in the calcareous caves near the small town of Lagoa Santa Minas Gerais Brazil Among the thousands of fossils found he recognized a few isolated cheek teeth as belonging to a hyena which he named Hyaena neogaea in 1839 After more material was found including canine teeth and foot bones Lund concluded the fossils instead belonged to a distinct genus of felids though transitional to the hyenas He stated it would have matched the largest modern predators in size and was more robust than any modern cat Lund originally wanted to name the new genus Hyaenodon but realizing this had recently become preoccupied by another prehistoric predator he instead named it Smilodon populator in 1842 He explained the Ancient Greek meaning of Smilodon as smilh smile scalpel or two edged knife and odontos odo ntos tooth This has also been translated as tooth shaped like double edged knife He explained the species name populator as the destroyer which has also been translated as he who brings devastation By 1846 Lund had acquired nearly every part of the skeleton from different individuals and more specimens were found in neighboring countries by other collectors in the following years 1 2 Though some later authors used Lund s original species name neogaea instead of populator it is now considered an invalid nomen nudum as it was not accompanied with a proper description and no type specimens were designated 3 Some South American specimens have been referred to other genera subgenera species and subspecies such as Smilodontidion riggii Smilodon Prosmilodon ensenadensis and S bonaeriensis but these are now thought to be junior synonyms of S populator 4 nbsp 1869 lithograph of the holotype molar and maxilla fragment of S fatalisFossils of Smilodon were discovered in North America from the second half of the 19th century onwards 1 In 1869 American paleontologist Joseph Leidy described a maxilla fragment with a molar which had been discovered in a petroleum bed in Hardin County Texas He referred the specimen to the genus Felis which was then used for most cats extant as well as extinct but found it distinct enough to be part of its own subgenus as F Trucifelis fatalis 5 The species name means deadly 6 In an 1880 article about extinct American cats American paleontologist Edward Drinker Cope pointed out that the F fatalis molar was identical to that of Smilodon and he proposed the new combination S fatalis 7 Most North American finds were scanty until excavations began in the La Brea Tar Pits in Los Angeles where hundreds of individuals of S fatalis have been found since 1875 1 S fatalis has junior synonyms such as S mercerii S floridanus and S californicus 4 American paleontologist Annalisa Berta considered the holotype of S fatalis too incomplete to be an adequate type specimen and the species has at times been proposed to be a junior synonym of S populator 3 Nordic paleontologists Bjorn Kurten and Lars Werdelin supported the distinctness of the two species in an article published in 1990 8 A 2018 article by the American paleontologist John P Babiarz and colleagues concluded that S californicus represented by the specimens from the La Brea Tar Pits was a distinct species from S fatalis after all and that more research is needed to clarify the taxonomy of the lineage 9 In his 1880 article about extinct cats Cope also named a third species of Smilodon S gracilis The species was based on a partial canine which had been obtained in the Port Kennedy Cave near the Schuylkill River in Pennsylvania Cope found the canine to be distinct from that of the other Smilodon species due to its smaller size and more compressed base 7 Its specific name refers to the species lighter build 10 This species is known from fewer and less complete remains than the other members of the genus 11 S gracilis has at times been considered part of genera such as Megantereon and Ischyrosmilus 12 S populator S fatalis and S gracilis are currently considered the only valid species of Smilodon and features used to define most of their junior synonyms have been dismissed as variation between individuals of the same species intraspecific variation 4 3 One of the most famous of prehistoric mammals Smilodon has often been featured in popular media and is the state fossil of California 1 Evolution edit nbsp Partial skull of S gracilis the earliest species in the genus Academy of Natural Sciences of PhiladelphiaLong the most completely known saber toothed cat Smilodon is still one of the best known members of the group to the point where the two concepts have been confused The term saber tooth itself refers to an ecomorph consisting of various groups of extinct predatory synapsids mammals and close relatives which convergently evolved extremely long maxillary canines as well as adaptations to the skull and skeleton related to their use This includes members of Gorgonopsia Thylacosmilidae Machaeroidinae Nimravidae Barbourofelidae and Machairodontinae 1 13 Within the family Felidae true cats members of the subfamily Machairodontinae are referred to as saber toothed cats and this group is itself divided into three tribes Metailurini false saber tooths Homotherini scimitar toothed cats and Smilodontini dirk toothed cats to which Smilodon belongs 4 Members of Smilodontini are defined by their long slender canines with fine to no serrations whereas Homotherini are typified by shorter broad and more flattened canines with coarser serrations 14 Members of Metailurini were less specialized and had shorter less flattened canines and are not recognized as members of Machairodontinae by some researchers 4 The earliest felids are known from the Oligocene of Europe such as Proailurus and the earliest one with saber tooth features is the Miocene genus Pseudaelurus 4 The skull and mandible morphology of the earliest saber toothed cats was similar to that of the modern clouded leopards Neofelis The lineage further adapted to the precision killing of large animals by developing elongated canine teeth and wider gapes in the process sacrificing high bite force 15 As their canines became longer the bodies of the cats became more robust for immobilizing prey 14 In derived smilodontins and homotherins the lumbar region of the spine and the tail became shortened as did the hind limbs 4 Based on mitochondrial DNA sequences extracted from fossils the lineages of Homotherium and Smilodon are estimated to have diverged about 18 Ma ago 16 The earliest species of Smilodon is S gracilis which existed from 2 5 million to 500 000 years ago early Blancan to Irvingtonian ages and was the successor in North America of Megantereon from which it probably evolved Megantereon itself had entered North America from Eurasia during the Pliocene along with Homotherium S gracilis reached the northern regions of South America in the Early Pleistocene as part of the Great American Interchange 17 14 S fatalis existed 1 6 million 10 000 years ago late Irvingtonian to Rancholabrean ages and replaced S gracilis in North America 8 S populator existed 1 million 10 000 years ago Ensenadan to Lujanian ages it occurred in the eastern parts of South America 18 Despite the colloquial name saber toothed tiger Smilodon is not closely related to the modern tiger which belongs in the subfamily Pantherinae or any other extant felid 19 A 1992 ancient DNA analysis suggested that Smilodon should be grouped with modern cats subfamilies Felinae and Pantherinae 20 A 2005 study found that Smilodon belonged to a separate lineage 21 A study published in 2006 confirmed this showing that the Machairodontinae diverged early from the ancestors of modern cats and were not closely related to any living species 22 The following cladogram based on fossils and DNA analysis shows the placement of Smilodon among extinct and extant felids after Rincon and colleagues 2011 17 nbsp S fatalis skeleton at National Museum of Natural History nbsp S populator statue in Tierpark BerlinFelidae ProailurusPseudaelurusPantherinae Panthera tigers lions jaguars and leopards nbsp Felinae Caracal nbsp Leopardus ocelot and relatives nbsp Felis domestic cats and relatives nbsp Herpailurus jaguarundi nbsp Miracinonyx nbsp Puma cougar nbsp Machairodontinae Dinofelis nbsp NimravidesMachairodus nbsp Homotherium nbsp Xenosmilus nbsp ParamachairodusMegantereonSmilodon gracilis nbsp Smilodon populator nbsp Smilodon fatalis nbsp Description edit nbsp Size of the three Smilodon species compared to a humanSkeleton edit Smilodon was around the size of modern big cats but was more robustly built It had a reduced lumbar region high scapula short tail and broad limbs with relatively short feet 23 24 Smilodon is most famous for its relatively long canine teeth which are the longest found in the saber toothed cats at about 28 cm 11 in long in the largest species S populator 23 The canines were slender and had fine serrations on the front and back side 25 The skull was robustly proportioned and the muzzle was short and broad The cheek bones zygomata were deep and widely arched the sagittal crest was prominent and the frontal region was slightly convex The mandible had a flange on each side of the front The upper incisors were large sharp and slanted forwards There was a diastema gap between the incisors and molars of the mandible The lower incisors were broad recurved and placed in a straight line across The p3 premolar tooth of the mandible was present in most early specimens but lost in later specimens it was only present in 6 of the La Brea sample 3 There is some dispute over whether Smilodon was sexually dimorphic Some studies of S fatalis fossils have found little difference between the sexes 26 27 Conversely a 2012 study found that while fossils of S fatalis show less variation in size among individuals than modern Panthera they do appear to show the same difference between the sexes in some traits 28 S gracilis was the smallest species estimated at 55 to 100 kg 120 to 220 lb in weight about the size of a jaguar It was similar to its predecessor Megantereon of the same size but its dentition and skull were more advanced approaching S fatalis 29 4 S fatalis was intermediate in size between S gracilis and S populator 23 It ranged from 160 to 280 kg 350 to 620 lb 29 and reached a shoulder height of 100 cm 39 in and body length of 175 cm 69 in 30 It was similar to a lion in dimensions but was more robust and muscular and therefore had a larger body mass Its skull was also similar to that of Megantereon though more massive and with larger canines 4 S populator was among the largest known felids with a body mass range from 220 kg 490 lb to over 400 kg 880 lb 29 and one estimate suggesting up to 470 kg 1 040 lb 31 A particularly large S populator skull from Uruguay measuring 39 2 cm 15 4 in in length indicates this individual may have weighed as much as 436 kg 961 lb 32 It stood at a shoulder height of 120 cm 47 in 23 Compared to S fatalis S populator was more robust and had a more elongated and narrow skull with a straighter upper profile higher positioned nasal bones a more vertical occiput more massive metapodials and slightly longer forelimbs relative to hindlimbs 4 8 Large fossil tracks from Argentina for which the ichnotaxon name Smilodonichium has been proposed have been attributed to S populator and measure 17 6 cm 6 9 in by 19 2 cm 7 6 in 33 This is larger than tracks of the Bengal tiger to which the footprints have been compared 34 External features edit nbsp nbsp S populator restored with plain coat by Charles R Knight in 1903 left and S fatalis restored with spotted coat right both of which are considered possibilities Smilodon and other saber toothed cats have been reconstructed with both plain colored coats and with spotted patterns which appears to be the ancestral condition for feliforms both of which are considered possible 35 Studies of modern cat species have found that species that live in the open tend to have uniform coats while those that live in more vegetated habitats have more markings with some exceptions 36 Some coat features such as the manes of male lions or the stripes of the tiger are too unusual to predict from fossils 35 Traditionally saber toothed cats have been artistically restored with external features similar to those of extant felids by artists such as Charles R Knight in collaboration with various paleontologists in the early 20th century 35 In 1969 paleontologist G J Miller instead proposed that Smilodon would have looked very different from a typical cat and similar to a bulldog with a lower lip line to allow its mouth to open wide without tearing the facial tissues a more retracted nose and lower placed ears 37 Paleoartist Mauricio Anton and coauthors disputed this in 1998 and maintained that the facial features of Smilodon were overall not very different from those of other cats Anton noted that modern animals like the hippopotamus are able to open their mouths extremely wide without tearing tissue due to a folded orbicularis oris muscle and such a muscle arrangement exists in modern large felids 38 Anton stated that extant phylogenetic bracketing where the features of the closest extant relatives of a fossil taxon are used as reference is the most reliable way of restoring the life appearance of prehistoric animals and the cat like Smilodon restorations by Knight are therefore still accurate 35 A 2022 study by Anton and colleagues concluded that the upper canines of Smilodon would have been visible when the mouth was closed while those of Homotherium would have not after examining fossils and extant big cats 39 Paleobiology editDiet edit nbsp S populator canine tooth the tip points to the rightAn apex predator Smilodon primarily hunted large mammals Isotopes preserved in the bones of S fatalis in the La Brea Tar Pits reveal that ruminants like bison Bison antiquus which was much larger than the modern American bison and camels Camelops were most commonly taken by the cats there 40 Smilodon fatalis may have also occasionally preyed upon Glyptotherium based on a skull from a juvenile Glyptotherium texanum recovered from Pleistocene deposits in Arizona that bear the distinctive elliptical puncture marks best matching those of Smilodon indicating that the predator successfully bit into the skull through the glyptodont s armored cephalic shield 41 In addition isotopes preserved in the tooth enamel of S gracilis specimens from Florida show that this species fed on the peccary Platygonus and the llama like Hemiauchenia 42 Stable carbon isotope measurements of S gracilis remains in Florida varied significantly between different sites and show that the species was flexible in its feeding habits 43 Isotopic studies of dire wolf Aenocyon dirus and American lion Panthera atrox bones show an overlap with S fatalis in prey which suggests that they were competitors 40 More detailed isotope analysis however indicates that Smilodon fatalis preferred forest dwelling prey such as tapirs deer and forest dwelling bison as opposed to the dire wolves preferences for prey inhabiting open areas such as grassland 44 The availability of prey in the Rancho La Brea area was likely comparable to modern East Africa 45 nbsp Two S populator stalking a Palaeolama group in BrazilAs Smilodon migrated to South America its diet changed bison were absent the horses and proboscideans were different and native ungulates such as toxodonts and litopterns were completely unfamiliar yet S populator thrived as well there as its relatives in North America 14 Isotopic analysis for S populator suggests that its main prey species included Toxodon platensis Pachyarmatherium Holmesina species of the genus Panochthus Palaeolama Catonyx Equus neogeus and the crocodilian Caiman latirostris This analysis of its diet also indicates that S populator hunted both in open and forested habitats 46 The differences between the North and South American species may be due to the difference in prey between the two continents 8 Smilodon may have avoided eating bone and would have left enough food for scavengers 47 Coprolites assigned to S populator recovered from Argentina preserve Mylodon osteoderms and a Lama scaphoid bone In addition to this unambiguous evidence of bone consumption the coprolites suggest that Smilodon had a more generalist diet than previously thought 48 Examinations of dental microwear from La Brea further suggests that Smilodon consumed both flesh and bone 49 Smilodon itself may have scavenged dire wolf kills 50 It has been suggested that Smilodon was a pure scavenger that used its canines for display to assert dominance over carcasses but this theory is not supported today as no modern terrestrial mammals are pure scavengers 51 Predatory behavior edit nbsp Tracks from Argentina which may have been produced by SmilodonThe brain of Smilodon had sulcal patterns similar to modern cats which suggests an increased complexity of the regions that control the sense of hearing sight and coordination of the limbs Felid saber tooths in general had relatively small eyes that were not as forward facing as those of modern cats which have good binocular vision to help them move in trees 51 Smilodon was likely an ambush predator that concealed itself in dense vegetation as its limb proportions were similar to modern forest dwelling cats 52 and its short tail would not have helped it balance while running 53 Unlike its ancestor Megantereon which was at least partially scansorial and therefore able to climb trees Smilodon was probably completely terrestrial due to its greater weight and lack of climbing adaptations 54 Tracks from Argentina named Felipeda miramarensis in 2019 may have been produced by Smilodon If correctly identified the tracks indicate that the animal had fully retractible claws plantigrade feet lacked strong supination capabilities in its paws notably robust forelimbs compared to the hindlimbs and was probably an ambush predator 55 The heel bone of Smilodon was fairly long which suggests it was a good jumper 23 Its well developed flexor and extensor muscles in its forearms probably enabled it to pull down and securely hold down large prey Analysis of the cross sections of S fatalis humeri indicated that they were strengthened by cortical thickening to such an extent that they would have been able to sustain greater loading than those of extant big cats or of the extinct American lion The thickening of S fatalis femurs was within the range of extant felids 56 Its canines were fragile and could not have bitten into bone due to the risk of breaking these cats had to subdue and restrain their prey with their powerful forelimbs before they could use their canine teeth and likely used quick slashing or stabbing bites rather than the slow suffocating bites typically used by modern cats 56 On rare occasions as evidenced by fossils Smilodon was willing to risk biting into bone with its canines This may have been focused more towards competition such as other Smilodon or potential threats such as other carnivores than on prey 54 nbsp Maximum gape of a saber toothed cat A and reconstructions of neck bite in prey of different sizes B C Debate continues as to how Smilodon killed its prey Traditionally the most popular theory is that the cat delivered a deep stabbing bite or open jawed stabbing thrust to the throat killing the prey very quickly 56 57 Another hypothesis suggests that Smilodon targeted the belly of its prey This is disputed as the curvature of their prey s belly would likely have prevented the cat from getting a good bite or stab 58 In regard to how Smilodon delivered its bite the canine shear bite hypothesis has been favored where flexion of the neck and rotation of the skull assisted in biting the prey but this may be mechanically impossible However evidence from comparisons with Homotherium suggest that Smilodon was fully capable of and utilized the canine shear bite as its primary means of killing prey based on the fact that it had a thick skull and relatively little trabecular bone while Homotherium had both more trabecular bone and a more lion like clamping bite as its primary means of attacking prey The discovery made by Figueirido and Lautenschlager et al published in 2018 suggests extremely different ecological adaptations in both machairodonts 59 The mandibular flanges may have helped resist bending forces when the mandible was pulled against the hide of a prey animal 60 nbsp nbsp S fatalis skull cast left and restoration by Mauricio Anton showing a wide gape The protruding incisors were arranged in an arch and were used to hold the prey still and stabilize it while the canine bite was delivered The contact surface between the canine crown and the gum was enlarged which helped stabilize the tooth and helped the cat sense when the tooth had penetrated to its maximum extent Since saber toothed cats generally had a relatively large infraorbital foramen opening in the skull which housed nerves associated with the whiskers it has been suggested the improved senses would have helped the cats precision when biting outside their field of vision and thereby prevent breakage of the canines The blade like carnassial teeth were used to cut skin to access the meat and the reduced molars suggest that they were less adapted for crushing bones than modern cats 51 As the food of modern cats enters the mouth through the side while cutting with the carnassials not the front incisors between the canines the animals do not need to gape widely so the canines of Smilodon would likewise not have been a hindrance when feeding 38 A study published in 2022 of how machairodonts fed revealed that wear patterns on the teeth of S fatalis also suggest that it was capable of eating bone to a similar extent as lions This and comparisons with bite marks left by the contemporary machairodont Xenosmilus suggest that Smilodon and its relatives could efficiently de flesh a carcass of meat when feeding without being hindered by their long canines 61 Despite being more powerfully built than other large cats Smilodon had a weaker bite Modern big cats have more pronounced zygomatic arches while these were smaller in Smilodon which restricted the thickness and therefore power of the temporalis muscles and thus reduced Smilodon s bite force Analysis of its narrow jaws indicates that it could produce a bite only a third as strong as that of a lion the bite force quotient measured for the lion is 112 62 63 There seems to be a general rule that the saber toothed cats with the largest canines had proportionally weaker bites Analyses of canine bending strength the ability of the canine teeth to resist bending forces without breaking and bite forces indicate that the saber toothed cats teeth were stronger relative to the bite force than those of modern big cats 64 In addition Smilodon s gape could have reached over 110 degrees 65 while that of the modern lion reaches 65 degrees 66 This made the gape wide enough to allow Smilodon to grasp large prey despite the long canines 38 A 2018 study compared the killing behavior of Smilodon fatalis and Homotherium serum and found that the former had a strong skull with little trabecular bone for a stabbing canine shear bite whereas the latter had more trabecular bone and used a clamp and hold style more similar to lions The two would therefore have held distinct ecological niches 67 Natural traps edit nbsp S fatalis fighting dire wolves over a Columbian mammoth carcass in the La Brea Tar Pits by Robert Bruce Horsfall 1913Many Smilodon specimens have been excavated from asphalt seeps that acted as natural carnivore traps Animals were accidentally trapped in the seeps and became bait for predators that came to scavenge but these were then trapped themselves The best known of such traps are at La Brea in Los Angeles which have produced over 166 000 Smilodon fatalis specimens 68 that form the largest collection in the world The sediments of the pits there were accumulated 40 000 to 10 000 years ago in the Late Pleistocene Though the trapped animals were buried quickly predators often managed to remove limb bones from them but they were themselves often trapped and then scavenged by other predators 90 of the excavated bones belonged to predators 69 The Talara Tar Seeps in Peru represent a similar scenario and have also produced fossils of Smilodon Unlike in La Brea many of the bones were broken or show signs of weathering This may have been because the layers were shallower so the thrashing of trapped animals damaged the bones of previously trapped animals Many of the carnivores at Talara were juveniles possibly indicating that inexperienced and less fit animals had a greater chance of being trapped Though Lund thought accumulations of Smilodon and herbivore fossils in the Lagoa Santa Caves were due to the cats using the caves as dens these are probably the result of animals dying on the surface and water currents subsequently dragging their bones to the floor of the cave but some individuals may also have died after becoming lost in the caves 69 Social life edit nbsp S fatalis pair approaching a group of the ground sloth Paramylodon one mired at the La Brea Tar Pits by Knight 1921Scientists debate whether Smilodon was social One study of African predators found that social predators like lions and spotted hyenas respond more to the distress calls of prey than solitary species Since S fatalis fossils are common at the La Brea Tar Pits and were likely attracted by the distress calls of stuck prey this could mean that this species was social as well 70 One critical study claims that the study neglects other factors such as body mass heavier animals are more likely to get stuck than lighter ones intelligence some social animals like the American lion may have avoided the tar because they were better able to recognize the hazard lack of visual and olfactory lures the type of audio lure and the length of the distress calls the actual distress calls of the trapped prey animals would have lasted longer than the calls used in the study The author of that study ponders what predators would have responded if the recordings were played in India where the otherwise solitary tigers are known to aggregate around a single carcass 71 The authors of the original study responded that though effects of the calls in the tar pits and the playback experiments would not be identical this would not be enough to overturn their conclusions In addition they stated that weight and intelligence would not likely affect the results as lighter carnivores are far more numerous than heavy herbivores and the social and seemingly intelligent dire wolf is also found in the pits 72 nbsp Lion pride attacking an African buffalo in Tanzania Smilodon may also have hunted in groupsAnother argument for sociality is based on the healed injuries in several Smilodon fossils which would suggest that the animals needed others to provide them food 73 74 This argument has been questioned as cats can recover quickly from even severe bone damage and an injured Smilodon could survive if it had access to water 75 However a Smilodon suffering hip dysplasia at a young age that survived to adulthood suggests that it could not have survived to adulthood without aid from a social group as this individual was unable to hunt or defend its territory due to the severity of its congenital issue 76 The brain of Smilodon was relatively small compared to other cat species Some researchers have argued that Smilodon s brain would have been too small for it to have been a social animal 77 An analysis of brain size in living big cats found no correlation between brain size and sociality 78 Another argument against Smilodon being social is that being an ambush hunter in closed habitat would likely have made group living unnecessary as in most modern cats 75 Yet it has also been proposed that being the largest predator in an environment comparable to the savanna of Africa Smilodon may have had a social structure similar to modern lions which possibly live in groups primarily to defend optimal territory from other lions lions are the only social big cats today 51 nbsp Tip of an S fatalis saber imbedded in the rib of another S fatalisWhether Smilodon was sexually dimorphic has implications for its reproductive behavior Based on their conclusions that Smilodon fatalis had no sexual dimorphism Van Valkenburgh and Sacco suggested in 2002 that if the cats were social they would likely have lived in monogamous pairs along with offspring with no intense competition among males for females 26 Likewise Meachen Samuels and Binder concluded in 2010 that aggression between males was less pronounced in S fatalis than in the American lion 27 Christiansen and Harris found in 2012 that as S fatalis did exhibit some sexual dimorphism there would have been evolutionary selection for competition between males 28 Some bones show evidence of having been bitten by other Smilodon possibly the result of territorial battles competition for breeding rights or over prey 51 Two S populator skulls from Argentina show seemingly fatal unhealed wounds which appear to have been caused by the canines of another Smilodon though it cannot be ruled out they were caused by kicking prey If caused by intraspecific fighting it may also indicate that they had social behavior which could lead to death as seen in some modern felines as well as indicating that the canines could penetrate bone 79 It has been suggested that the exaggerated canines of saber toothed cats evolved for sexual display and competition but a statistical study of the correlation between canine and body size in S populator found no difference in scaling between body and canine size concluded it was more likely they evolved solely for a predatory function 80 A set of three associated skeletons of S fatalis found in Ecuador and described in 2021 by Reynolds Seymour and Evans suggests that there was prolonged parental care in Smilodon The two subadult individuals uncovered share a unique inherited trait in their dentaries suggesting they were siblings a rare instance of familial relationships being found in the fossil record The subadult specimens are also hypothesized to have been male and female respectively while the adult skeletal remains found at the site are believed to have belonged to their mother The subadults were estimated to have been around two years of age at the time of their deaths but were still growing 81 S fatalis had proportionally larger hyoid bones than modern felid species and thus likely produced deeper vocalizations While Smilodon had the same number of hyoid bones as the roaring cats their shape was closer to that of purring species 82 Development edit nbsp Undersides of S fatalis skulls showing canine replacement George C Page MuseumSmilodon started developing its adult saber teeth when the animal reached between 12 and 19 months of age shortly after the completion of the eruption of the cat s baby teeth Both baby and adult canines would be present side by side in the mouth for an approximately 11 month period and the muscles used in making the powerful bite were developed at about one and a half years old as well eight months earlier than in a modern lion After Smilodon reached 23 to 30 months of age the infant teeth were shed while the adult canines grew at an average growth rate of 7 mm 0 3 in per month during a 12 month period They reached their full size at around 3 years of age later than modern species of big cats Juvenile and adolescent Smilodon specimens are extremely rare at Rancho La Brea where the study was performed indicating that they remained hidden or at denning sites during hunts and depended on parental care while their canines were developing 83 84 85 A 2017 study indicates that juveniles were born with a robust build similar to the adults Comparison of the bones of juvenile S fatalis specimens from La Brea with those of the contemporaneous American lion revealed that the two cats shared a similar growth curve Felid forelimb development during ontogeny changes during growth has remained tightly constrained The curve is similar to that for modern cats such as tigers and cougars but shifts more towards the robust direction of the axes than is seen in modern felids 86 Examinations by Reynolds Seymour and Evans 2021 suggest that Smilodon had a unique and fast growth rate similar to a tiger but that there was a prolonged period of growth in the genus similar to what is seen in lions and that the cubs were reliant on their parents until this growth period ended 81 Paleopathology edit nbsp Large subchondral defects in S fatalis limb joints arrows Several Smilodon fossils show signs of ankylosing spondylitis hyperostosis and trauma 87 One study of 1 000 Smilodon skulls found that 36 of them had eroded parietal bones which is where the largest jaw muscles attach They also showed signs of microfractures and the weakening and thinning of bones possibly caused by mechanical stress from the constant need to make stabbing motions with the canines 88 Bony growths where the deltoid muscle inserted in the humerus is a common pathology for a La Brea specimen which was probably due to repeated strain when Smilodon attempted to pull down prey with its forelimbs Sternum injuries are also common probably due to collision with prey 89 The frequency of trauma in S fatalis specimens was 4 3 compared to 2 8 in the dire wolf which implies the ambush predatory behavior of the former led to greater risk of injury than the pursuit predatory behavior of the latter Smilodon remains exhibit relatively more shoulder and lumbar vertebrae injuries 90 A 2023 study documented a high degree of subchondral defects in limb joint surfaces of S fatalis and dire wolf specimens from the La Brea Tar pits that resembled osteochondrosis dissecans As modern dogs with this disease are inbred the researchers suggested this would have been the case for the prehistoric species as well as they approached extinction but cautioned that more research was needed to determine if this was also the case in specimens from other parts of the Americas 91 Osteomyelitis in the left fourth metacarpal bone has been reported in a S populator specimen dating back to Marine Isotope Stage 5 This pathology resulted in the machairodont individual becoming incapable of flexing its toe and would have severely diminished its ability to hunt prey 92 Distribution and habitat edit nbsp Environment of what is now White Sands National Park with S fatalis in the reeds in the right foregroundSmilodon lived during the Pleistocene epoch 2 5 mya 10 000 years ago and was perhaps the most recent of the saber toothed cats 23 It probably lived in closed habitat such as forest or bush 93 Fossils of the genus have been found throughout the Americas 3 The northernmost remains of the genus are S fatalis fossils from Alberta Canada 94 with the southernmost remains being known from the far south of Patagonia 95 The habitat of North America varied from subtropical forests and savannah in the south to treeless mammoth steppes in the north The mosaic vegetation of woods shrubs and grasses in southwestern North America supported large herbivores such as horses bison antelope deer camels mammoths mastodons and ground sloths North America also supported other saber toothed cats such as Homotherium and Xenosmilus as well as other large carnivores including dire wolves short faced bear Arctodus simus and the American lion 14 69 96 Competition from such carnivores may have prevented North American S fatalis from attaining the size of South America s S populator The similarity in size of S fatalis and the American lion suggests niche overlap and direct competition between these species and they appear to have fed on similarly sized prey 97 nbsp Animals that participated in the Great American Interchange with North American migrants like S populator lower right in blueS gracilis entered South America during the early to middle Pleistocene where it probably gave rise to S populator which lived in the eastern part of the continent S fatalis also entered western South America in the late Pleistocene and the two species were thought to be divided by the Andes mountains 8 17 23 However in 2018 a skull of S fatalis found in Uruguay east of the Andes was reported which puts the idea that the two species were allopatric geographically separated into question 98 The American interchange resulted in a mix of native and invasive species sharing the prairies and woodlands in South America North American herbivores included proboscideans horses camelids and deer South American herbivores included toxodonts litopterns ground sloths and glyptodonts Native metatherian predators including the saber toothed thylacosmilids had gone extinct by the Pliocene and were replaced by North American carnivores such as canids bears and large cats 14 S populator was very successful while Homotherium never became widespread in South America The extinction of the thylacosmilids has been attributed to competition with Smilodon but this is probably incorrect as they seem to have disappeared before the arrival of the large cats The phorusrhacid terror birds may have dominated the large predator niche in South America until Smilodon arrived 14 S populator may have been able to reach larger size than S fatalis due to a lack of competition in Pleistocene South America S populator arrived after the extinction of Arctotherium angustidens one of the largest carnivores ever and could therefore assume the niche of mega carnivore 97 S populator preferred large prey from open habitats such as grassland and plains based on evidence gathered from isotope ratios that determined the animal s diet In this way the South American Smilodon species was probably similar to the modern lion S populator probably competed with the canid Protocyon there but not with the jaguar which fed primarily on smaller prey 99 100 On the other hand morphometry points to S populator being best adapted for more closed environments 101 Extinction edit nbsp Skeletons of S fatalis left and the American lion two large North American felids which went extinct during the Late Pleistocene George C Page MuseumAlong with most of the New World Pleistocene megafauna Smilodon became extinct by 10 000 years ago in the late Pleistocene extinction phases of North and South America Its extinction has been linked to the decline and extinction of large herbivores Hence Smilodon could have been too specialized at hunting large prey and may have been unable to adapt 56 Indeed by the Bolling Allerod warming event and before the Younger Dryas cooling event S fatalis showed changes in cranial morphology that hint towards increased specialization in larger prey and or evolution in response to competition with other carnivores 102 However a 2012 study of Smilodon tooth wear found no evidence that they were limited by food resources 103 Other explanations include climate change and competition with Homo sapiens 103 who entered the Americas around the time Smilodon disappeared or a combination of several factors all of which apply to the general Late Pleistocene extinction event rather than specifically to the extinction of the saber toothed cats 104 One factor often cited here is the cooling in the Younger Dryas which may have drastically reduced the habitable space for many species In terms of human influence there is evidence of a fire induced regime change in Rancho la Brea that preceded the extirpation of megafauna in the area with humans most likely responsible for the increase in fire intensity 105 Writers of the first half of the twentieth century theorized that the last saber toothed cats Smilodon and Homotherium became extinct through competition with the faster and more generalized felids that replaced them It was even proposed that the saber toothed predators were inferior to modern cats as the ever growing canines were thought to inhibit their owners from feeding properly Since then however it has been shown that the diet of machairodontines such as Smilodon and Homotherium was diverse They do not seem to have been limited to giant animals as prey as suggested before but fed on whatever was available including bovines equines and camelids 106 107 Additionally non machairodontine felids such as the American lion and Miracinonyx also became extinct during the Late Pleistocene and saber toothed and conical toothed felids had formerly coexisted for more than a million years 108 The fact that saber teeth evolved many times in unrelated lineages also attests to the success of this feature 104 nbsp Skeletal diagram of S populatorThe youngest direct radiocarbon date for S fatalis differs from that of S populator by thousands of years the former just before the Younger Dryas cooling event and the latter by the early Holocene 109 The latest S fatalis specimen recovered from the Rancho La Brea tar pits has been dated to 13 025 years ago 110 A specimen of S fatalis from Iowa dates to 13 605 13 455 years Before Present BP 111 The latest Smilodon populator remains found in the cave of Cueva del Medio near the town of Soria northeast Ultima Esperanza Province Magallanes Region in southernmost Chile have been dated to 10 935 11 209 years ago 112 The most recent credible carbon 14 date for S fatalis has been given as 11 130 BP 113 However such radiocarbon dates are likely uncalibrated meaning that they were not adjusted from calendar years to regular years As a result the dates appear younger than they actually are Therefore the S fatalis specimen from Rancho La Brea is the youngest recorded of the species 109 suggesting extinction before the Younger Dryas based on its last appearance in California as opposed to other regions where megafauna declined by the Younger Dryas 105 See also edit nbsp Biology portal nbsp Paleontology portalList of largest carnivorans List of largest prehistoric carnivorans Megafauna Late Pleistocene extinctionsReferences edit a b c d e Anton 2013 pp 3 26 Lund P W 1842 Blik paa Brasiliens Dyreverden for sidste Jordomvaeltning in Danish Copenhagen Det Kongelige Danske Videnskabernes Selskabs Naturvidenskabelige og Matematiske Afhandlinger pp 54 57 a b c d e Berta A 1985 The status of Smilodon in North and South America PDF Contributions in Science Natural History Museum of Los Angeles County 370 1 15 Archived from the original PDF on 28 May 2014 a b c d e f g h i j Anton 2013 pp 108 154 Leidy J 1869 The extinct mammalian fauna of Dakota and Nebraska Including an account of some allied forms from other localities together with a synopsis of the mammalian remains of North America Journal of the Academy of Natural Sciences of Philadelphia 7 366 367 doi 10 5962 bhl title 20910 Sabertooth National Geographic 21 September 2011 Retrieved 2021 10 13 a b Cope E D December 1880 On the extinct cats of America The American Naturalist 14 12 833 858 doi 10 1086 272672 JSTOR 2449549 a b c d e Kurten B Werdelin L 1990 Relationships between North and South American Smilodon Journal of Vertebrate Paleontology 10 2 158 169 Bibcode 1990JVPal 10 158K doi 10 1080 02724634 1990 10011804 JSTOR 4523312 Werdelin L McDonald H G Shaw C A 2018 Smilodon The Iconic Sabertooth Smilodon from South Carolina Implications for the taxonomy of the genus ed Baltimore Johns Hopkins University Press pp 76 95 ISBN 978 1 4214 2557 3 Kurten B Anderson E 1980 Pleistocene Mammals of North America New York Columbia University Press pp 186 188 ISBN 978 0 231 03733 4 Berta A 1987 The sabercat Smilodon gracilis from Florida and a discussion of its relationships Mammalia Felidae Smilodontini Bulletin of the Florida State Museum 31 1 63 Churcher C S 1984 The status of Smilodontopsis Brown 1908 and Ischyrosmilus Merriam 1918 a taxonomic review of two genera of sabretooth cats Felidae Machairodontinae Royal Ontario Museum Life Sciences Contributions 140 14 34 doi 10 5962 bhl title 52222 ISBN 978 0 88854 305 9 Meehan T Martin L D J 2003 Extinction and re evolution of similar adaptive types ecomorphs in Cenozoic North American ungulates and carnivores reflect van der Hammen s cycles Die Naturwissenschaften 90 3 131 135 Bibcode 2003NW 90 131M doi 10 1007 s00114 002 0392 1 PMID 12649755 S2CID 21117744 a b c d e f g Anton 2013 pp 65 76 Christiansen P 2008 Evolution of skull and mandible shape in cats Carnivora Felidae PLOS ONE 3 7 e2807 Bibcode 2008PLoSO 3 2807C doi 10 1371 journal pone 0002807 PMC 2475670 PMID 18665225 nbsp Paijmans J L A Barnett R Gilbert M T P Zepeda Mendoza M L Reumer J W F de Vos J Zazula G Nagel D Baryshnikov G F Leonard J A Rohland N Westbury M V Barlow A Hofreiter M 2017 10 19 Evolutionary History of Saber Toothed Cats Based on Ancient Mitogenomics Current Biology 27 21 3330 3336 e5 Bibcode 2017CBio 27E3330P doi 10 1016 j cub 2017 09 033 PMID 29056454 a b c Rincon A Prevosti F Parra G 2011 New saber toothed cat records Felidae Machairodontinae for the Pleistocene of Venezuela and the Great American Biotic Interchange Journal of Vertebrate Paleontology 31 2 468 478 Bibcode 2011JVPal 31 468R doi 10 1080 02724634 2011 550366 hdl 11336 69016 JSTOR 25835839 S2CID 129693331 de Castro Mariela Cordeiro Langer Max Cardoso 2008 New postcranial remains of Smilodon populator Lund 1842 from South Central Brazil Revista Brasileira de Paleontologia 11 3 199 206 doi 10 4072 rbp 2008 3 06 What Is a Sabertooth University of California Museum of Paleontology December 2005 Retrieved 2012 06 12 Janczewski D N Yuhki N Gilbert D A Jefferson G T O Brien S J 1992 Molecular phylogenetic inference from saber toothed cat fossils of Rancho La Brea Proceedings of the National Academy of Sciences 89 20 9769 9773 Bibcode 1992PNAS 89 9769J doi 10 1073 pnas 89 20 9769 PMC 50214 PMID 1409696 Barnett R Barnes I Phillips M J Martin L D Harington C R Leonard J A Cooper A 2005 Evolution of the extinct sabretooths and the American cheetah like cat Current Biology 15 15 R589 R590 Bibcode 2005CBio 15 R589B doi 10 1016 j cub 2005 07 052 PMID 16085477 S2CID 17665121 van den Hoek Ostende L W Morlo M Nagel D 2006 Majestic killers the sabre toothed cats Fossils explained 52 Geology Today 22 4 150 157 doi 10 1111 j 1365 2451 2006 00572 x S2CID 128960196 a b c d e f g Turner A Anton M 1997 The Big Cats and Their Fossil Relatives An Illustrated Guide to Their Evolution and Natural History Columbia University Press pp 57 58 67 68 ISBN 978 0 231 10229 2 OCLC 34283113 What Is a Sabertooth University of California Museum of Paleontology Retrieved 2013 04 08 Slater G J Valkenburgh B V 2008 Long in the tooth evolution of sabertooth cat cranial shape Paleobiology 34 3 403 419 Bibcode 2008Pbio 34 403S doi 10 1666 07061 1 ISSN 0094 8373 S2CID 85353590 a b Van Valkenburgh B Sacco T 2002 Sexual dimorphism social behavior and intrasexual competition in large Pleistocene carnivorans Journal of Vertebrate Paleontology 22 1 164 169 doi 10 1671 0272 4634 2002 022 0164 sdsbai 2 0 co 2 JSTOR 4524203 S2CID 86156959 a b Meachen Samuels J Binder W 2010 Sexual dimorphism and ontogenetic growth in the American lion and sabertoothed cat from Rancho La Brea Journal of Zoology 280 3 271 279 doi 10 1111 j 1469 7998 2009 00659 x a b Christiansen Per Harris John M 2012 Variation in Craniomandibular Morphology and Sexual Dimorphism in Pantherines and the Sabercat Smilodon fatalis PLOS ONE 7 10 e48352 Bibcode 2012PLoSO 748352C doi 10 1371 journal pone 0048352 PMC 3482211 PMID 23110232 a b c Christiansen Per Harris John M 2005 Body size of Smilodon Mammalia Felidae Journal of Morphology 266 3 369 84 doi 10 1002 jmor 10384 PMID 16235255 S2CID 27233870 Saber Toothed Cat Smilodon fatalis San Diego Zoo Global January 2009 Archived from the original on 2013 02 03 Retrieved 2013 05 07 Sorkin B 2008 A biomechanical constraint on body mass in terrestrial mammalian predators Lethaia 41 4 333 347 Bibcode 2008Letha 41 333S doi 10 1111 j 1502 3931 2007 00091 x Manzuetti A Perea D Jones W Ubilla M Rinderknecht A 2020 An extremely large saber tooth cat skull from Uruguay late Pleistocene early Holocene Dolores Formation body size and paleobiological implications Alcheringa An Australasian Journal of Palaeontology 44 2 332 339 Bibcode 2020Alch 44 332M doi 10 1080 03115518 2019 1701080 S2CID 216505747 Hallazgo inedito en Miramar huellas fosilizadas de un gran tigre dientes de sable 0223 com ar in Spanish 0223 May 26 2016 Retrieved 28 May 2016 Perkins Sid June 10 2016 First fossil footprints of saber toothed cats are bigger than Bengal tiger paws Science doi 10 1126 science aag0602 a b c d Anton 2013 pp 157 176 Allen W L Cuthill I C Scott Samuel N E Baddeley R 2010 Why the leopard got its spots relating pattern development to ecology in felids Proceedings of the Royal Society B 278 1710 1373 1380 doi 10 1098 rspb 2010 1734 PMC 3061134 PMID 20961899 Miller G J 1969 A new hypothesis to explain the method of food ingestion used by Smilodon californicus Bovard Tebiwa 12 9 19 a b c Anton M Garcia Perea R Turner A 1998 Reconstructed facial appearance of the sabretoothed felid Smilodon Zoological Journal of the Linnean Society 124 4 369 386 doi 10 1111 j 1096 3642 1998 tb00582 x Anton Mauricio Siliceo Gema Pastor Juan F Salesa Manuel J 2022 Concealed weapons A revised reconstruction of the facial anatomy and life appearance of the sabre toothed cat Homotherium latidens Felidae Machairodontinae Quaternary Science Reviews 284 107471 Bibcode 2022QSRv 28407471A doi 10 1016 j quascirev 2022 107471 hdl 10261 270770 S2CID 248168629 a b Coltrain J B Harris J M Cerling T E Ehleringer J R Dearing M D Ward J Allen J 2004 Rancho La Brea stable isotope biogeochemistry and its implications for the palaeoecology of late Pleistocene coastal southern California PDF Palaeogeography Palaeoclimatology Palaeoecology 205 3 4 199 219 Bibcode 2004PPP 205 199C doi 10 1016 j palaeo 2003 12 008 Archived from the original PDF on November 11 2011 Anton 2013 pp 203 204 Feranec R S 2005 Growth rate and duration of growth in the adult canine of S gracilis and inferences on diet through stable isotope analysis PDF Bulletin of the Florida Museum of Natural History 45 4 369 377 doi 10 58782 flmnh psyo5090 via University of Florida Feranec Robert S DeSantis Larisa R G Summer 2014 Understanding specifics in generalist diets of carnivorans by analyzing stable carbon isotope values in Pleistocene mammals of Florida Paleobiology 40 3 477 493 Bibcode 2014Pbio 40 477F doi 10 1666 13055 ISSN 0094 8373 Retrieved 21 January 2024 via Cambridge Core DeSantis Larisa R G Crites Jonathan M Feranec Robert S Fox Dobbs Kena Farrell Aisling B Harris John M Takeuchi Gary T Cerling Thure E 2019 Causes and Consequences of Pleistocene Megafaunal Extinctions as Revealed from Rancho La Brea Mammals Current Biology 29 15 2488 2495 Bibcode 2019CBio 29E2488D doi 10 1016 j cub 2019 06 059 PMID 31386836 Vanvalkenburgh B Hertel F 1993 Tough Times at La Brea Tooth Breakage in Large Carnivores of the Late Pleistocene Science 261 5120 456 459 Bibcode 1993Sci 261 456V doi 10 1126 science 261 5120 456 PMID 17770024 S2CID 39657617 Dantas Mario Andre Trindade Cherkinsky Alexander Lessa Carlos Micael Bonfim Santos Luciano Vilaboim Cozzuol Mario Alberto Omena Erica Cavalcante Silva Jorge Luiz Lopes Sial Alcides Nobrega Bocherens Herve 2020 07 14 Isotopic paleoecology d13C d18O of a late Pleistocene vertebrate community from the Brazilian Intertropical Region Revista Brasileira de Paleontologia 23 2 138 152 doi 10 4072 rbp 2020 2 05 ISSN 2236 1715 Van Valkenburgh B Teaford M F Walker A 1990 Molar microwear and diet in large carnivores inferences concerning diet in the sabretooth cat Smilodon fatalis Journal of Zoology 222 2 319 340 doi 10 1111 j 1469 7998 1990 tb05680 x Moreno Rodriguez Ana P Chimento Nicolas R Agnolin Federico L Jofre Guillermo Gentil Adriel 2022 A possible Smilodon Mammalia Felidae Coprolite from the Pleistocene of Argentina PALAIOS 37 7 402 410 Bibcode 2022Palai 37 402M doi 10 2110 palo 2021 056 ISSN 1938 5323 S2CID 251078622 DeSantis Larisa R G Shaw Christopher A 2018 Sabertooth Cats with Toothaches Impacts of Dental Injuries on Feeding Behavior in Late Pleistocene Smilodon Fatalis Mammalia Felidae from Rancho la Brea Los Angeles California Geological Society of America Abstracts with Programs 50 6 322567 doi 10 1130 abs 2018AM 322567 Van Valkenburgh B 1991 Iterative evolution of hypercarnivory in canids Mammalia Carnivora evolutionary interactions among sympatric predators Paleobiology 17 4 340 362 Bibcode 1991Pbio 17 340V doi 10 1017 S0094837300010691 JSTOR 2400749 S2CID 251052044 a b c d e Anton 2013 pp 176 216 Gonyea W J 1976 Behavioral implications of saber toothed felid morphology Paleobiology 2 4 332 342 Bibcode 1976Pbio 2 332G doi 10 1017 S0094837300004966 JSTOR 2400172 S2CID 87481727 What Is a Sabertooth Berkeley edu Retrieved 1 June 2017 a b Anton Mauricio 2013 Sabertooth Agnolin F L Chimento N R Campo D H Magnussen M Boh D De Cianni F 2019 Large Carnivore Footprints from the Late Pleistocene of Argentina Ichnos 26 2 119 126 Bibcode 2019Ichno 26 119A doi 10 1080 10420940 2018 1479962 S2CID 134190731 a b c d Meachen Samuels J A Van Valkenburgh B 2010 Radiographs reveal exceptional forelimb strength in the sabertooth cat Smilodon fatalis PLOS ONE 5 7 e11412 Bibcode 2010PLoSO 511412M doi 10 1371 journal pone 0011412 ISSN 1932 6203 PMC 2896400 PMID 20625398 nbsp McHenry C R Wroe S Clausen P D Moreno K Cunningham E 2007 Supermodeled sabercat predatory behavior in Smilodon fatalis revealed by high resolution 3D computer simulation PNAS 104 41 16010 16015 Bibcode 2007PNAS 10416010M doi 10 1073 pnas 0706086104 PMC 2042153 PMID 17911253 Anyonge W 1996 Microwear on canines and killing behavior in large carnivores saber function in Smilodon fatalis Journal of Mammalogy 77 4 1059 1067 doi 10 2307 1382786 JSTOR 1382786 Figueirido B Lautenschlager S Perez Ramos A Van Valkenburgh B 2018 Distinct Predatory Behaviors in Scimitar and Dirk Toothed Sabertooth Cats Current Biology 28 20 3260 3266 e3 Bibcode 2018CBio 28E3260F doi 10 1016 j cub 2018 08 012 hdl 10630 29727 PMID 30293717 Brown J G 2014 Jaw function in Smilodon fatalis a reevaluation of the canine shear bite and a proposal for a new forelimb powered class 1 lever model PLOS ONE 9 10 e107456 Bibcode 2014PLoSO 9j7456B doi 10 1371 journal pone 0107456 ISSN 1932 6203 PMC 4182664 PMID 25272032 nbsp Dominguez Rodrigo Manuel Egeland Charles P Cobo Sanchez Lucia Baquedano Enrique Hulbert Richard C 2022 Sabertooth carcass consumption behavior and the dynamics of Pleistocene large carnivoran guilds Scientific Reports 12 1 6045 Bibcode 2022NatSR 12 6045D doi 10 1038 s41598 022 09480 7 PMC 9061710 PMID 35501323 Hecht J 1 October 2007 Sabre tooth cat had a surprisingly delicate bite New Scientist Wroe S McHenry2 C Thomason J 2004 Bite club comparative bite force in big biting mammals and the prediction of predatory behaviour in fossil taxa PDF Proceedings of the Royal Society 272 1563 619 25 doi 10 1098 rspb 2004 2986 PMC 1564077 PMID 15817436 Archived from the original PDF on 2013 08 25 a href Template Cite journal html title Template Cite journal cite journal a CS1 maint numeric names authors list link Christiansen P 2007 Comparative bite forces and canine bending strength in feline and sabretooth felids implications for predatory ecology Zoological Journal of the Linnean Society 151 2 423 437 doi 10 1111 j 1096 3642 2007 00321 x Andersson K Norman D Werdelin L 2011 Sabretoothed carnivores and the killing of large prey PLOS ONE 6 10 e24971 Bibcode 2011PLoSO 624971A doi 10 1371 journal pone 0024971 PMC 3198467 PMID 22039403 nbsp Martin L D 1980 Functional morphology and the evolution of cats Transactions of the Nebraska Academy of Sciences 8 141 154 Figueirido B Lautenschlager S Perez Ramos A Van Valkenburgh B 2018 Distinct Predatory Behaviors in Scimitar and Dirk Toothed Sabertooth Cats Current Biology 28 20 3260 3266 e3 Bibcode 2018CBio 28E3260F doi 10 1016 j cub 2018 08 012 hdl 10630 29727 PMID 30293717 Shaw Christopher A Quinn James P September 15 2015 John M Harris ed The Addition of Smilodon fatalis Mammalia Carnivora Felidae to the Biota of the Late Pleistocene Carpinteria Asphalt Deposits in California with Ontogenetic and Ecologic Implications for the Species PDF Science Series 42 Contributions in Science A special volume entitled La Brea and Beyond the Paleontology of Asphalt Preserved Biotas in commemoration of the 100th anniversary of the Natural History Museum of Los Angeles County s excavations at Rancho La Brea Natural History Museum of Los Angeles County 91 95 Archived from the original PDF on December 25 2016 Retrieved September 30 2017 a b c Anton 2013 pp 30 33 Carbone C Maddox T Funston P J Mills M G L Grether G F Van Valkenburgh B 2009 Parallels between playbacks and Pleistocene tar seeps suggest sociality in an extinct sabretooth cat Smilodon Biology Letters 5 1 81 85 doi 10 1098 rsbl 2008 0526 PMC 2657756 PMID 18957359 Kiffner C 2009 Coincidence or evidence was the sabretooth cat Smilodon social Biology Letters 5 4 561 562 doi 10 1098 rsbl 2009 0008 PMC 2781900 PMID 19443504 Van Valkenburgh B Maddox T Funston P J Mills M G L Grether G F Carbone C 2009 Sociality in Rancho La Brea Smilodon arguments favour evidence over coincidence Biology Letters 5 4 563 564 doi 10 1098 rsbl 2009 0261 PMC 2781931 Heald F 1989 Injuries and diseases in Smilodon californicus Bovard 1904 Mammalia Felidae from Rancho La Brea California Journal of Vertebrate Paleontology 9 3 24A Balisi M A Sharma A K Howard C M Shaw C A Klapper R Lindsey Emily L 2020 Computed tomography reveals hip dysplasia in Smilodon Implications for social behavior in an extinct Pleistocene predator bioRxiv 10 1101 2020 01 07 897348 a b McCall S Naples V Martin L 2003 Assessing behavior in extinct animals was Smilodon social Brain Behavior and Evolution 61 3 159 164 doi 10 1159 000069752 PMID 12697957 S2CID 2756104 Balisi Mairin A Sharma Abhinav K Howard Carrie M Shaw Christopher A Klapper Robert Lindsey Emily L 2021 Computed tomography reveals hip dysplasia in the extinct Pleistocene saber tooth cat Smilodon bioRxiv 11 1 21271 doi 10 1101 2020 01 07 897348 PMC 8553773 PMID 34711910 S2CID 235663241 Radinsky L B 1975 Evolution of the felid brain Brain Behavior and Evolution 11 3 4 214 254 doi 10 1159 000123636 PMID 1181005 Yamaguchi N Kitchener A C Gilissen E MacDonald D W 2009 Brain size of the lion Panthera leo and the tiger P tigris implications for intrageneric phylogeny intraspecific differences and the effects of captivity Biological Journal of the Linnean Society 98 1 85 93 doi 10 1111 j 1095 8312 2009 01249 x Chimento N R Agnolin F L Soibelzon L Ochoa J G Buide V 2019 Evidence of intraspecific agonistic interactions in Smilodon populator Carnivora Felidae Comptes Rendus Palevol 18 4 449 454 Bibcode 2019CRPal 18 449C doi 10 1016 j crpv 2019 02 006 O Brien D M 2019 Static scaling and the evolution of extreme canine size in a saber toothed cat Smilodon fatalis Integrative and Comparative Biology 59 5 1303 1311 doi 10 1093 icb icz054 PMID 31120517 a b Reynolds Ashley R Seymour Kevin L Evans David C January 7 2021 Smilodon fatalis siblings reveal life history in a saber toothed cat iScience 24 1 101916 Bibcode 2021iSci 24j1916R doi 10 1016 j isci 2020 101916 PMC 7835254 PMID 33532710 Deutsch A R Langerhans R B Flores D Hartstone Rose A 2023 The roar of Rancho La Brea Comparative anatomy of modern and fossil felid hyoid bones Journal of Morphology 284 10 e21627 doi 10 1002 jmor 21627 PMID 37708512 S2CID 261090355 Dagger like canines of saber toothed cats took years to grow ScienceDaily 2015 07 01 Archived from the original on 2015 07 02 Retrieved 2015 07 02 Mihlbachler M C Wysocki M A Feranec R S Tseng Z J Bjornsson C S 2015 07 01 Using a novel absolute ontogenetic age determination technique to calculate the timing of tooth eruption in the saber toothed cat Smilodon fatalis PLOS ONE 10 7 e0129847 Bibcode 2015PLoSO 1029847W doi 10 1371 journal pone 0129847 PMC 4489498 PMID 26132165 nbsp Feranec R C 2004 Isotopic evidence of saber tooth development growth rate and diet from the adult canine of Smilodon fatalis from Rancho La Brea Palaeogeography Palaeoclimatology Palaeoecology 206 3 4 303 310 Bibcode 2004PPP 206 303F doi 10 1016 j palaeo 2004 01 009 Long K Prothero D Madan M Syverson V J P Smith T 2017 Did saber tooth kittens grow up musclebound A study of postnatal limb bone allometry in felids from the Pleistocene of Rancho La Brea PLOS ONE 12 9 e0183175 Bibcode 2017PLoSO 1283175L doi 10 1371 journal pone 0183175 PMC 5617143 PMID 28953899 Bjorkengren A G Sartoris D J Shermis S Resnick D 1987 Patterns of paravertebral ossification in the prehistoric saber toothed cat American Journal of Roentgenology 148 4 779 782 doi 10 2214 ajr 148 4 779 PMID 3103404 Duckler G L 1997 Parietal depressions in skulls of the extinct saber toothed felid Smilodon fatalis evidence of mechanical strain Journal of Vertebrate Paleontology 17 3 600 609 Bibcode 1997JVPal 17 600D doi 10 1080 02724634 1997 10011006 Anton 2013 p 199 Brown C Balisi M Shaw C A Van Valkenburgh B 2017 Skeletal trauma reflects hunting behaviour in extinct sabre tooth cats and dire wolves Nature Ecology amp Evolution 1 5 0131 Bibcode 2017NatEE 1 131B doi 10 1038 s41559 017 0131 PMID 28812696 S2CID 8008808 Schmokel Hugo Farrell Aisling Balisi Mairin F 2023 Subchondral defects resembling osteochondrosis dissecans in joint surfaces of the extinct saber toothed cat Smilodon fatalis and dire wolf Aenocyon dirus PLOS ONE 18 7 e0287656 Bibcode 2023PLoSO 1887656S doi 10 1371 journal pone 0287656 PMC 10337945 PMID 37436967 Luna Carlos A Pool Roy R Ercoli Marcos D Chimento Nicolas R Barbosa Fernando H de S Zurita Alfredo E Cuaranta Pedro 22 May 2023 Osteomyelitis in the manus of Smilodon populator Felidae Machairodontinae from the Late Pleistocene of South America Palaeoworld doi 10 1016 j palwor 2023 05 001 ISSN 1871 174X Retrieved 5 February 2024 via Elsevier Science Direct Meloro C Elton S Louys J Bishop L C Ditchfield P 2013 Cats in the forest predicting habitat adaptations from humerus morphometry in extant and fossil Felidae Carnivora PDF Paleobiology 39 3 323 344 Bibcode 2013Pbio 39 323M doi 10 1666 12001 S2CID 83957027 Reynolds A R Seymour K L Evans D C 2019 Late Pleistocene records of felids from Medicine Hat Alberta including the first Canadian record of the sabre toothed cat Smilodon fatalis Canadian Journal of Earth Sciences 56 10 1052 1060 Bibcode 2019CaJES 56 1052R doi 10 1139 cjes 2018 0272 hdl 1807 96725 S2CID 134586651 Villavicencio Natalia A Lindsey Emily L Martin Fabiana M Borrero Luis A Moreno Patricio I Marshall Charles R Barnosky Anthony D February 2016 Combination of humans climate and vegetation change triggered Late Quaternary megafauna extinction in the Ultima Esperanza region southern Patagonia Chile Ecography 39 2 125 140 Bibcode 2016Ecogr 39 125V doi 10 1111 ecog 01606 ISSN 0906 7590 DeSantis L R G Schubert B W Schmitt Linville E Ungar P Donohue S Haupt R J September 15 2015 John M Harris ed Dental microwear textures of carnivorans from the La Brea Tar Pits California and potential extinction implications PDF Science Series 42 Contributions in Science A special volume entitled La Brea and Beyond the Paleontology of Asphalt Preserved Biotas in commemoration of the 100th anniversary of the Natural History Museum of Los Angeles County s excavations at Rancho La Brea Natural History Museum of Los Angeles County 37 52 Archived from the original PDF on December 20 2016 Retrieved February 6 2017 a b Sherani S 2016 A new specimen dependent method of estimating felid body mass No e2327v2 PeerJ Preprints Manzuetti A Perea D Ubilla M Rinderknecht A 2018 First record of Smilodon fatalis Leidy 1868 Felidae Machairodontinae in the extra Andean region of South America late Pleistocene Sopas Formation Uruguay Taxonomic and paleobiogeographic implications Quaternary Science Reviews 180 57 62 Bibcode 2018QSRv 180 57M doi 10 1016 j quascirev 2017 11 024 Bocherens H Cotte M Bonini R Scian D Straccia P Soibelzon L Prevosti F J 2016 04 24 Paleobiology of sabretooth cat Smilodon population in the Pampean Region Buenos Aires Province Argentina around the Last Glacial Maximum Insights from carbon and nitrogen stable isotopes in bone collagen Palaeogeography Palaeoclimatology Palaeoecology 449 463 474 Bibcode 2016PPP 449 463B doi 10 1016 j palaeo 2016 02 017 Hays B 2016 03 21 Saber toothed cats were the lions of prehistoric South America UPI Science News UPI Retrieved 19 April 2016 Meloro Carlo Elton Sarah Louys Julien Bishop Laura C Ditchfield Peter 18 March 2013 Cats in the forest predicting habitat adaptations from humerus morphometry in extant and fossil Felidae Carnivora Paleobiology 39 3 323 344 Bibcode 2013Pbio 39 323M doi 10 1666 12001 ISSN 0094 8373 Retrieved 21 January 2024 via Cambridge Core Meachen Julie A O Keefe F Robin Sadleir Rudyard W 2014 Evolution in the sabre tooth cat Smilodon fatalis in response to Pleistocene climate change Journal of Evolutionary Biology 27 4 714 723 doi 10 1111 jeb 12340 PMID 24779050 a b DeSantis L R G Schubert B W Scott J R Ungar P S 2012 Implications of diet for the extinction of saber toothed cats and American lions PLOS ONE 7 12 e52453 Bibcode 2012PLoSO 752453D doi 10 1371 journal pone 0052453 PMC 3530457 PMID 23300674 nbsp a b Anton 2013 pp 217 230 a b O Keefe F Robin Dunn Regan E Weitzel Elic M Waters Michael R Martinez Lisa N Binder Wendy J Southon John R Cohen Joshua E Meachen Julie A DeSantis Larisa R G Kirby Matthew E Ghezzo Elena Coltrain Joan B Fuller Benjamin T Farrell Aisling B Takuechi Gary T MacDonald Glen Davis Edward B Lindsey Emily L 2023 Pre Younger Dryas megafaunal extirpation at Rancho La Brea linked to fire driven state shift Science 381 6659 eabo3594 doi 10 1126 science abo3594 PMID 37590347 Bocherens Herve 2015 06 01 Isotopic tracking of large carnivore palaeoecology in the mammoth steppe Quaternary Science Reviews 117 42 71 Bibcode 2015QSRv 117 42B doi 10 1016 j quascirev 2015 03 018 ISSN 0277 3791 Prevosti Francisco J Martin Fabiana M 2013 08 14 Paleoecology of the mammalian predator guild of Southern Patagonia during the latest Pleistocene Ecomorphology stable isotopes and taphonomy Quaternary International Ranked habitats and the process of human colonization of South America 305 74 84 Bibcode 2013QuInt 305 74P doi 10 1016 j quaint 2012 12 039 hdl 11336 84524 ISSN 1040 6182 Anton 2013 p 223 a b Stuart Anthony J August 20 2022 Chapter 6 North America mastodon ground sloths and sabertooth cats Vanished Giants The Lost World of the Ice Age University of Chicago Press pp 67 112 ISBN 978 0 226 82403 1 O Keefe F R Fet E V Harris J M 2009 Compilation calibration and synthesis of faunal and floral radiocarbon dates Rancho La Brea California Contributions in Science 518 1 16 doi 10 5962 p 226783 S2CID 128107590 Hill Matthew G Easterla David A May 2023 A complete sabertooth cat cranium from the Midcontinent of North America and its evolutionary and ecological context Quaternary Science Reviews 307 108045 Bibcode 2023QSRv 30708045H doi 10 1016 j quascirev 2023 108045 S2CID 257861663 Prieto Alfredo Labarca Rafael Sierpe Victor 2010 New evidence of the sabertooth cat Smilodon Carnivora Machairodontinae in the late Pleistocene of southern Chilean Patagonia Revista Chilena de Historia Natural 83 2 doi 10 4067 S0716 078X2010000200010 Fiedel Stuart 2009 Sudden Deaths The Chronology of Terminal Pleistocene Megafaunal Extinction PDF In Haynes Gary ed American Megafaunal Extinctions at the End of the Pleistocene Vertebrate Paleobiology and Paleoanthropology Springer pp 21 37 doi 10 1007 978 1 4020 8793 6 2 ISBN 978 1 4020 8792 9 Bibliography edit nbsp Wikimedia Commons has media related to Smilodon category nbsp Wikispecies has information related to Smilodon Anton M 2013 Sabertooth 1st ed Bloomington Indiana University Press ISBN 978 0 253 01042 1 OCLC 857070029 Retrieved from https en wikipedia org w index php title Smilodon amp oldid 1217826035, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.