Homotherium Explained

Homotherium is an extinct genus of scimitar-toothed cat belonging to the extinct subfamily Machairodontinae that inhabited North America, South America, Eurasia, and Africa during the Pliocene and Pleistocene epochs from around 4 million to 12,000 years ago.[1] It was one of the last surviving members of the subfamily alongside the more famous sabertooth Smilodon, to which it was distantly related. It was a large cat, comparable in size to a lion. In comparison to Smilodon, the canines of Homotherium were shorter (though still longer than those of living cats), and it was probably adapted to running down rather than ambushing prey, and is suggested to have engaged in cooperative hunting.

History and taxonomy

Eurasia

The first fossils of this genus were described in 1846 by Richard Owen as the species Machairodus latidens.[2] The name Homotherium (Greek: Greek, Ancient (to 1453);: ὁμός ('same') and Greek, Ancient (to 1453);: θηρίον ('beast')) was proposed by Emilio Fabrini (1890), without further explanation, for a new subgenus of Machairodus, whose main distinguishing feature was the presence of a large diastema between the two inferior premolars. He further described two species in this new subgenus: Machairodus (Megantereon) crenatidens and Machairodus (Megantereon) nestianus.[3] In 1918, the species Homotherium moravicum was described by Woldřich.[4] In 1936, Teilhard de Chardin described the new species Homotherium ultimus based on fossils from the middle Pleistocene-aged site at Zhoukoudian.[5] In 1972, a species Homotherium davitašvlii was described based on fragmentary material found at Kvabebi in Georgia.[6] Further material from Odessa was tentatively assigned to this species in 2004.[7] In 1986, the species Homotherium darvasicum was described based on material from Kuruksay, Turkey.[8] In 1989, another species Homotherium tielhardipiveteaui was named based on fossils from Tajikistan.[9] In 1996, Homotherium hengduanshanense was described based on fossils from the Hengduan Mountains.[10]

There is currently only one recognised species Homotherium in Eurasia during the Late Pliocene-Pleistocene, Homotherium latidens; other species, including H. nestianus, H. sainzelli, H. crenatidens, H. nihowanensis, and H. ultimum, were proposed mainly on size differences, and do not appear to be distinct.

Africa

In 1972 a species Homotherium problematicum (originally Megantereon problematicus) was named based on fragmentary material from Africa.[11] A second African species discovered in Ethiopia, Homotherium hadarensis, was described in 1988.[12] In 1990, Alan Turner challenged the validity of these two species, and later authors typically refrained from referring the African fossils to any specific species. Although in 2015, further material from Dikika was tentatively referred to H. hadarensis.[13]

A third species, Homotherium africanum (originally Machairodus africanus), has also been included.[14] [15] [16]

Americas

In 1905, Merriam described a new species Machaerodus ischyrus.[17] Subsequently, in 1918, Merriam reassigned it to a new genus Ischyrosmilus along with the new species Ischyrosmilus idahoensis.[18] The genus Dinobastis was originally named by Cope in 1893, with the type species Dinobastis serus.[19] In 1965, the species Ischyrosmilus johnstoni was described. In the same paper, it was noted that a comparative study of both Ischyrosmilus and Homotherium might conclude them as synonyms.[20]

In 1966, Churcher named Dinobastis a junior synonym of Homotherium, and recombined D. serus as Homotherium serum.[21] In 1970, a new species Ischyrosmilus crusafonti was described from the early Pleistocene of Nebraska.[22] In 1988, after some debate, the genus Ischyrosmilus was declared a junior synonym of Homotherium and all four species were reassigned to that genus as H. ischyrus, H. idahoensis, and H. johnstoni. The same paper also proposed keeping Dinobastis serus separate from Homotherium.[23] Up to five species have been recognised from North America: H. idahoensis, H. crusafonti, H. ischyrus, H. johnstoni, and H. serum,[24] while other authors suggest that there are only two species, with older Blancan specimens are assigned to the species H. ischyrus, while the younger ones are assigned to the species H. serum.

In 2005, a new species Homotherium venezuelensis was described based on fossils from the Pleistocene of Venezuela.[25] In 2022, it was proposed that Homotherium venezuelensis be reassigned to the genus Xenosmilus.[26]

Evolutionary history

The lineage of Homotherium is estimated (based on mitochondrial DNA sequences) to have diverged from that of Smilodon about 18 million years ago.[27] Homotherium has been suggested to have originated from African species of the genus Amphimachairodus.[28] Homotherium first appeared during the Early Pliocene, about 4 million years ago, with its oldest remains being from the Odesa catacombs in Ukraine, and Koobi Fora in Kenya, which are close in age, making the origin location of the genus uncertain. The genus arrived in North America during the late Pliocene.[29] Specimens of Homotherium are known from Venezuela in northern South America, of an uncertain Early-Middle Pleistocene age.[30] On the African continent the genus disappeared about 1.5 million years ago, during the Early Pleistocene.[31] The latest records of Homotherium in Europe date to the late Middle Pleistocene, around 300-200,000 years ago,[32] with the exception of a single lower jaw bone from the North Sea which dates to around 28-30,000 years ago.[33] The mitochondrial genome of this specimen is nearly identical to specimens known from North America, suggesting that this may have represented a Late Pleistocene dispersal from North America, rather than a continuous undocumented occupation of the region. Homotherium became extinct in North America around 12,000 years ago as part of the end-Pleistocene extinctions of most large mammals across the Americas.[34]

Description

Homotherium reached 1.1m (03.6feet) at the shoulder and weighed an estimated 190kg (420lb) and was therefore about the size of a male lion.[35] [36] Homotherium had shorter upper canines than other machariodonts such as Smilodon or Megantereon, but these were still longer than those of extant cats. The incisors and lower canines of Homotherium formed a powerful puncturing and gripping device, and its large canine teeth were crenulated. The jaws of Homotherium may have been adapted to clamp and hold prey while inflicting damage with the canine teeth, due to comparable amounts of trabecular bone present in skulls of the genus to those of the modern lion.[37]

The large upper canines of Homotherium, which are distinctly flattened,[38] were likely hidden by the upper lips and gum tissues of the lower lips jaw similar to extant cats, unlike the larger upper canines of Smilodon. This hypothesis is further supported by comparable space between the canines and mandible at full closure of the jaws to modern cats; while Smilodon has significantly more space in this respect, likely for soft tissue to fit between the canine and mandible.[39]

Compared to Smilodon, the legs were proportionally longer, and the forelimbs were less powerfully built, being narrow and intermediate in form between those of cheetahs and lions. The neck was relatively long and had a high degree of flexibility, while the back was relatively short. The claws were small and semi-rectractable, the dewclaw being large, with the second phalanges being less asymmetrical than those of lions, giving the feet a dog-like posture. The part of the humerus closest to the foot was narrow, with the olecranon fossa being strongly vertical. The hindfeet were held in a raised digitigrade posture. Homotherium likely walked with a posture intermediate between that of living big cats and hyenas, similar to that of canines. The tail was very short.

Diet and habitats

The reduced claws, relatively slender limbs, and sloping back all appear to be adaptations for endurance running in open habitats.[40] It has been speculated based on its adaptation to open habitats and high levels of competition from other carnivores, that Homotherium probably relied on group hunting.

Genomic analysis supports the hypothesis that Homotherium was social and well-adapted to life as a pursuit predator. The study also revealed that this genus of machairodont was most likely diurnal, and would have mainly hunted in daylight.[41]

African Homotherium species seem to have hunted early Pleistocene species of Deinotherium, likely preferring to target the more vulnerable adolescents or calves in a herd. Due to their saber-teeth, an attack on such thick-skinned prey would have likely been significantly easier and less time-consuming compared to a similar hunt on modern elephants by lions.[42]

At the well known Friesenhahn Cave site in Texas, the remains of almost 400 juvenile mammoths were discovered along with numerous Homotherium skeletons of all ages, from elderly specimens to cubs. Based on this fossil site, Homotherium was likely a social predator that would have been specialized in hunting young mammoths and that subsequently dragged the kills into secluded caves to eat in relative peace. Homotherium also seemed to have retained the excellent nocturnal vision typical of most cats, and hunting at night in the arctic regions where many Homotherium have been found would have been a prime hunting method.[43] The sloped back and powerful lumbar section of Homotheriums vertebrae suggest a bear-like build, and thus that these animals could have been capable of pulling formidable loads; further, broken upper canines - a common injury in fossils of other machairodonts such as Machairodus and Smilodon that would have resulted from struggling with their prey - is not seen in Homotherium, perhaps because their social groups would completely restrain prey items before any of the cats attempted to kill the target with their saber teeth. Moreover, the bones of the young mammoths found in Friesenhahn Cave show distinctive marks matching the incisors of Homotherium, indicating that they could efficiently process most of the meat on a carcass and that the mammoths had been deposited in the caves by the cats themselves and not by scavengers. Examination of the bones also indicates that the carcasses of these juvenile mammoths were dismembered after being killed by the cats before being dragged away, suggesting that Homotherium would disarticulate their kill to transport it to a safe area such as a hidden lair or den and prevent competitors such as dire wolves and American lions from usurping the carcass.[44] Isotopic analysis of H. serum dental remains have confirmed it fed on mammoths, along with other C4 grazers.[45]

External links

Notes and References

  1. Book: A. . Turner . 'The big cats and their fossil relatives . Columbia University Press . 1997 .
  2. Book: Owen, Richard. A History of British Mammals and Birds. 1846.
  3. Fabrini. E.. 1890. I Machairodus (Meganthereon) del Val d'Arno superiore. Bollettino Comitato Geologico d'Italia. it. 21. 121–144, 161–177.
  4. Woldřich . J. . 1916 . První nálezy Machaerodů v jeskynním diluviu moravském a dolnorakouském . Rozpravy České akademie cís. Fr. Josefa pro vědy, slovesnost a umění, třída II . 25 . 12 . 1–8 . Czech.
  5. P. Teilhard de Chardin . Fossil mammals from Locality 9 of Choukoutien . Palaeontol. Sin. Ser. C . 7 . 1936 . 1–61.
  6. A.K. Vekua . Kvabebskaya Fauna Akchagyl'skikh pozvonochnykh . The Kvabebi Fauna of Akchagylian Vertebrates . 1972.
  7. M. V. Sotnikova . New data on the Pliocene carnivore fauna of Odessa Catacombs . 199–202 . Problems of Stratigraphy of the Phanerozoic of Ukraine. Institute of Geological Sciences, Kiev . 2004.
  8. Scharapov, S. . 1986 . Kuruksajskij kompleks pozdnepliocenovych mlekopitajushchikh Afgano-Tadshikskoj depressii . Duanbe (Donis) . 272.
  9. S. Scharapov . On a new species of the saber-toothed cat from the Late Eopleistocene of the Afgano-Tadjik depression and the evolution of the genus Homotherium Fabrini, 1890 . Paleontological Journal, Moscow . 3 . 1989 . 73–83.
  10. Zong, G. . 1996 . Cenozoic mammals and environment of Hengduan Mountains region . China Ocean Press.
  11. Collings . G.E.. A new species of machairodont from Makapansgat . Palaeont. Afr. . 14 . 1972 . 87–92.
  12. G. Petter . F.C. Howell . Nouveau felidé machairodonte (Mammalia, Carnivora) de la faune pliocène de l'Afar (Ethiopie) Homotherium hadarensis n. sp . C. R. Acad. Sci. Paris . 306 . 1988 . 731–738.
  13. 10.1016/j.jafrearsci.2015.03.020 . Pliocene Carnivora (Mammalia) from the Hadar Formation at Dikika, Lower Awash Valley, Ethiopia . 2015 . Geraads . Denis . Alemseged . Zeresenay . Bobe . René . Reed . Denné . Journal of African Earth Sciences . 107 . 28–35 . 2015JAfES.107...28G .
  14. Arambourg . C. . 1970 . Les vértébres du Pléistocène de l'Afrique du Nord . Archives du Muséum national d'Histoire naturelle . 10 . 1–127.
  15. Petter . G. . Howell . F.C. . 1987 . Machairodus africanus Arambourg, 1970 (Carnivora, Mammalia) du Villafranchien d'Aïn Brimba, Tunisie . Bulletin du Muséum National d'Histoire Naturelle, Paris, 4Eme SEr., C, 9 . 4 . 97–119 .
  16. 10.1016/j.jhevol.2017.05.001 . A contextual review of the Carnivora of Kanapoi . 2020 . Werdelin . Lars . Lewis . Margaret E. . Journal of Human Evolution . 140 . 28625408 . 2020JHumE.14002334W . 23285088 .
  17. Merriam . J. C. . 1905 . A new saber-tooth from California . Univ. Calif. Publ. B Geol. . 4 . 171–175.
  18. Merriam . J. C. . 1918 . New mammalia from the Idaho formation . Univ. Calif. Publ. Bull. Dept. Geol. . 10 . 523–530.
  19. Cope . E.D. . A new Pleistocene sabre-tooth . The American Naturalist . 27 . 1893 . 896–897.
  20. Mawby . John E. . 1965 . Machairodonts from the Late Cenozoic of the Panhandle of Texas . Jour. Mammal. . 46 . 4 . 573–587 . 10.2307/1377928 . 1377928.
  21. Churcher . C. S. . 1966 . The affinities of Dinobastis serus Cope 1893 . Quaternaria . 8 . 263–275.
  22. Machairodont Cats from the Early Pleistocene Broadwater and Lisco Local Faunas . Bulletin of the University of Nebraska State Museum . November 1970 . Schultz . C. . Martin . Larry .
  23. Martin . Larry D. . Schultz . C. B. . Schultz . M. R. . Saber-Toothed Cats from the Plio-Pleistocene of Nebraska . 1988 . Transactions of the Nebraska Academy of Sciences and Affiliated Societies . 186 .
  24. Book: L.D. Martin . V.L. Naples . J.P. Babiarz . Revision of the new World Homotheriini . The Other Saber-tooths: Scimitar-tooth Cats of the Western Hemisphere . Johns Hopkins University Press . Baltimore . 2011 . 185–194.
  25. Rincón . Ascanio D. . Prevosti . Francisco J. . Parra . Gilberto E. . 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 . 10.1080/02724634.2011.550366 . 25835839 . 2011JVPal..31..468R . 129693331. 11336/69016 . free .
  26. Jiangzuo . Q. . Werdelin . L. . Sun . Y. . 2022 . A dwarf sabertooth cat (Felidae: Machairodontinae) from Shanxi, China, and the phylogeny of the sabertooth tribe Machairodontini . Quaternary Science Reviews . 284 . Article 107517 . 10.1016/j.quascirev.2022.107517. 2022QSRv..28407517J .
  27. Paijmans . Johanna L.A. . Barnett . Ross . Gilbert . M. Thomas P. . Zepeda-Mendoza . M. Lisandra . Reumer . Jelle W.F. . de Vos . John . Zazula . Grant . Nagel . Doris . Baryshnikov . Gennady F. . Leonard . Jennifer A. . Rohland . Nadin . Westbury . Michael V. . Barlow . Axel . Hofreiter . Michael . Evolutionary History of Saber-Toothed Cats Based on Ancient Mitogenomics . Current Biology . November 2017 . 27 . 21 . 3330–3336.e5 . 10.1016/j.cub.2017.09.033 . 29056454 . free . 2017CBio...27E3330P .
  28. Lihoreau . Fabrice . Sarr . Raphaël . Chardon . Domininique . Boisserie . Jean-Renaud . Lebrun . Renaud . Adnet . Sylvain . Martin . Jeremy E. . Pallas . Laurent . Sambou . Bernard . Tabuce . Rodolphe . Thiam . Mohamadou M. . Hautier . Lionel . November 2021 . A fossil terrestrial fauna from Tobène (Senegal) provides a unique early Pliocene window in western Africa . Gondwana Research . en . 99 . 21–35 . 10.1016/j.gr.2021.06.013. free . 2021GondR..99...21L .
  29. Antón . M. . Salesa . M.J. . Galobart . A. . Tseng . Z.J. . July 2014 . The Plio-Pleistocene scimitar-toothed felid genus Homotherium Fabrini, 1890 (Machairodontinae, Homotherini): diversity, palaeogeography and taxonomic implications . Quaternary Science Reviews . en . 96 . 259–268 . 10.1016/j.quascirev.2013.11.022. 2014QSRv...96..259A .
  30. Rincón . Ascanio D. . Prevosti . Francisco J. . Parra . Gilberto E. . 17 March 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 . 10.1080/02724634.2011.550366 . 2011JVPal..31..468R . 129693331. 11336/69016 . free .
  31. Turner . Alan . 1990 . The evolution of the guild of larger terrestrial carnivores during the Plio-Pleistocene in Africa . Geobios . 23 . 3 . 349–368 . 10.1016/0016-6995(90)80006-2. 1990Geobi..23..349T .
  32. Diedrich . Cajus G. . McFarlane . Donald A. . 29 April 2017 . Homotherium from Middle Pleistocene archaeological and carnivore den sites of Germany – Taxonomy, taphonomy and a revision of the Schöningen, West Runton and other saber-tooth cat sites . . en . 436 . 76–83 . 10.1016/j.quaint.2016.10.015 . 2017QuInt.436...76D . 20 July 2024 . Elsevier Science Direct.
  33. Reumer . Jelle W. F. . Rook . Lorenzo . Van Der Borg . Klaas . Post . Klaas . Mol . Dick . De Vos . John . 11 April 2003 . Late Pleistocene survival of the saber-toothed cat Homotherium in northwestern Europe . Journal of Vertebrate Paleontology . 23 . 1 . 260–262 . 10.1671/0272-4634(2003)23[260:LPSOTS]2.0.CO;2 . 140187064.
  34. Ewald . Tatyanna . Hills . L.V. . Tolman . Shayne . Kooyman . Brian . January 2018 . Scimitar cat (Homotherium serum Cope) from southwestern Alberta, Canada . Canadian Journal of Earth Sciences . en . 55 . 1 . 8–17 . 10.1139/cjes-2017-0130 . 2018CaJES..55....8E . 0008-4077. 1807/79756 . free .
  35. Sorkin. Boris. 2008. A biomechanical constraint on body mass in terrestrial mammalian predators. Lethaia. 41. 4. 333–347. 10.1111/j.1502-3931.2007.00091.x. 2008Letha..41..333S .
  36. Meade, G.E. 1961: The saber-toothed cat Dinobastis serus. Bulletin of the Texas Memorial Museum 2(II), 23–60.
  37. Figueirido . Borja . Lautenschlager . Stephan . Pérez-Ramos . Alejandro . Van Valkenburgh . Blaire . Distinct Predatory Behaviors in Scimitar- and Dirk-Toothed Sabertooth Cats . Current Biology . October 2018 . 28 . 20 . 3260–3266.e3 . 10.1016/j.cub.2018.08.012 . 30293717 . free . 2018CBio...28E3260F . 10630/29727 . free .
  38. Mauricio Antón Behaviour of Homotherium in the light of modern African big cats N.J. Conard, K.F. Hillgruber, J. Serangeli, T. Terberger (Eds.), The Homotherium Finds from Schöningen 13 II-4: Man and Big Cats of the Ice Age, Schnell & Steiner, Regensburg (2021), pp. 9-23
  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 . 10.1016/j.quascirev.2022.107471. free . 2022QSRv..28407471A . 10261/270770 . free .
  40. Anton . M . Galobart . A . Turner . A . Co-existence of scimitar-toothed cats, lions and hominins in the European Pleistocene. Implications of the post-cranial anatomy of (Owen) for comparative palaeoecology . Quaternary Science Reviews . May 2005 . 24 . 10–11 . 1287–1301 . 10.1016/j.quascirev.2004.09.008 .
  41. Barnett . Ross . Westbury . Michael V. . Sandoval-Velasco . Marcela . Vieira . Filipe Garrett . Jeon . Sungwon . Zazula . Grant . Martin . Michael D. . Ho . Simon Y. W. . Mather . Niklas . Gopalakrishnan . Shyam . Ramos-Madrigal . Jazmín . Manuel . Marc de . Zepeda-Mendoza . M. Lisandra . Antunes . Agostinho . Baez . Aldo Carmona . Cahsan . Binia De . Larson . Greger . O'Brien . Stephen J. . Eizirik . Eduardo . Johnson . Warren E. . Koepfli . Klaus-Peter . Wilting . Andreas . Fickel . Jörns . Dalén . Love . Lorenzen . Eline D. . Marques-Bonet . Tomas . Hansen . Anders J. . Zhang . Guojie . Bhak . Jong . Yamaguchi . Nobuyuki . Gilbert . M. Thomas P. . Genomic Adaptations and Evolutionary History of the Extinct Scimitar-Toothed Cat, Homotherium latidens . Current Biology . 21 December 2020 . 30 . 24 . 5018–5025.e5 . 10.1016/j.cub.2020.09.051 . 33065008 . 7762822 . 2020CBio...30E5018B .
  42. Web site: Deinotheres for lunch? A sabertooth's tough-skinned diet. 2017-03-23.
  43. Metcalfe . Jessica . Late Pleistocene climate and proboscidean paleoecology in North America: Insights from stable isotope compositions of skeletal remains . 2011 .
  44. Book: Antón, Mauricio. Sabertooth. 2013. University of Indiana Press. Bloomington, Indiana. 978-0-253-01042-1. 227–228.
  45. DeSantis . Larisa R. G. . Feranec . Robert S. . Antón . Mauricio . Lundelius . Ernest L. . 21 June 2021 . Dietary ecology of the scimitar-toothed cat Homotherium serum . . en . 31 . 12 . 2674–2681.e3 . 10.1016/j.cub.2021.03.061 . free . 33862006 . 2021CBio...31E2674D .