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Albanosmilus

From Wikipedia, the free encyclopedia
Extinct genus of carnivores

Albanosmilus
Cranium ofAlbanosmilus jourdani
Scientific classificationEdit this classification
Kingdom:Animalia
Phylum:Chordata
Class:Mammalia
Order:Carnivora
Family:Nimravidae
Tribe:Barbourofelini
Genus:Albanosmilus
Kretzoi, 1929
Type species
Albanosmilus jourdani
(Filhol, 1883)
Other Species
  • Albanosmilus whitfordi(Barbour & Cook, 1915)
Synonyms

A. jourdani

  • Albanosmilus vallesiensis
  • Barbourofelis vallesiensis
  • Sansanosmilus jourdani

A. whitfordi

  • Barbourofelis whitfordi

Albanosmilus is an extinctgenus of the subfamilyBarbourofelinae, part of the family of feliforms known asNimravidae.[1] The genus currently consists of two named species:Albanosmilus jourdani andAlbanosmilus whitfordi.Albanosmilus lived inEurasia andNorth America from theMiddle toLate Miocene from 12 to 7mya, making it one of the last nimravids.[2][3] The genus may have been ancestral toBarbourofelis.

A. jourdani was found in Eurasia and was the largest species of the genus. With estimates suggesting it could've weighed 80–100 kg (180–220 lb), making it as large as ajaguar and smaller thanBarbourofelis. LikeBarbourofelis,A. jourdani was believed to have been an ambulatory,ambush predator and was likely anapex predator of its ecosystem.A. whitfordi was endemic to North America and was smaller in size, more similar in size aleopard. UnlikeA. jourdani,A. whitfordi was believed to have been acursorial predator. In addition,Albanosmilus was also recovered in East Asia.

Taxonomy

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Classification

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Bryant in his 1991 consideredAlbanosmilus as a member of the falsesabre-toothed cat familyNimravidae.[4] However,Albanosmilus was eventually considered part of the Barbourofelidae, where it was considered synonymous toSansanosmilus. By 2013, this was refuted as the authors argued it had features that differed fromSansanosmilus such as larger size, more reduced p3, and displaying a double fused or single root. It also had features differed fromBarbourofelis including the presence of a mesial cingulum cusp in P3 and lack of metaconid in m1. In the addition, the authors also movedBarbourofelis whitfordi to the genusAlbanosmilus.[2]

In the 2020s, majority of experts reclassified barbourofelids as nimravids, either as a subfamily known as Barbourofelinae, or within the subfamilyNimravine.[5][6][7][8][9][1][10]

Evolution

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According to recent phylogenetic analysis, Barbourofelins likely evolved whenNimravinae dispersed intoAfrica. Their size was likely constrained due to the diversity ofhyaenodonts that roamed continent. Despite this, they were still able to carve a niche due to their dental morphology. Eventually they would disperse into Eurasia and North America.[7] During the late Middle Miocene,A. jourdani replacedSansanosmilus in Europe.[11]

A. jourdani may have migrated into North America and evolved into the genusBarbourofelis and the speciesA. whitfordi.[12]

Description

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Albanosmilus jourdani is estimated to have weighed around 80–100 kg (180–220 lb),[13][14] one study suggested this species could've even exceeded 100 kg (220 lb).[15] Making it one of the largestnimravids, just behindBarbourofelis,Dinailurictis,Eusmilus adelos, andQuercylurus.

A. whitfordi was considered to be similar in size toB. morrisi, which was as large as aleopard.[16][17] A 2024 study found based on m1 regressions estimated thatA. whitfordi could've weighed 72.8 kg (160 lb).[18]Including supplementary materials

Paleobiology

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Albanosmilus is speculated to either have been apack or solitary hunter.[13][14] A 2020 study estimated thatA. jourdani had a jaw gape of 90 degrees.[19]Including supplementary materials Coprolites likely referable to this genus were described in 2023, which may suggest thatAlbanosmilus was an apex predator in this locality. Presumably, like other carnivorans that weighed over 25 kg (55 lb), it probably hunted herbivores its size or larger. Due to the lack of bone fragments, it's suggested that the diet ofAlbanosmilus largely consisted of meat, which is consistent with its hypercarnviorous dentition and presumed nutrients.[14] WhileA. jourdani was recovered as anambush, ambulatory predator,[14][15]A. whitfordi has been recovered as acursorial predator based on elbow morphology.[20]

Paleoecology

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Albanosmilus jourdani was found in Eurasia, and lived from 11.9-9.1 Ma.[13][7]Including supplementary materials This species was found inGratkorn, it coexisted with herbivores such as would includeequidAnchitherium,suids such asParachleuastochoerus steinheimensis andlistriodontinaeListriodon splendens,palaeomerycidaePalaeomeryx,chalicotheriidaeChalicotherium,aceratheriinae rhinosAceratherium,Brachypotherium andLartetotherium, anddeinotheriinae proboscideanDeinotherium. The contemporarycarnivoran within this locality was the hyenaProtictitherium, both carnivores would've coexisted by hunting prey of different sizes. Based on the coprolites, equid, suids, and palaeomerycids were probable prey forAlbanosmilus. While on the other hand, chalicotheres, rhinos, and proboscideans were would've been improbable prey, with social hunting comparable tolion prides being required to hunt young proboscideans. On the other hand, there is possible evidence ofAlbanosmilus scavenging onDeinotherium.[14]

Within Los Valles de Fuentidueña,A. jourdani coexisted with carnivorans includingfelids such as the basalPseudaelurus quadridentatus andmachairodontMachairodus aphanistus,amphicyoninaeMagericyon castellanus, andictitheriinae hyenaLycyaenachaeretis. Herbivores within this locality includehipparionini equidHippotherium primigenium, aceratheriinae rhinosAceratherium incisivum andAlicornops simorrense,bovidMiotragocerus,cervidEuprox dicranocerus,tragulidDorcatheriumnaui,giraffidDecennatherium pachecoi, and "tetralophodontgomphothere"Tetralophodon longirostris. Isotopic analysis showsAlbanosmilus hunted in woodland to mesic grasslands and preyed uponHippotherium,Miotragocerus,Euprox,Dorcatherium, andChalicomys.Miotragocerus was found to make the greatest contribution to its diet whileDorcatherium was the least contributor. They also found that the megaherbivores were unlikely to have been frequent prey items by any of the carnivorans. The isotopic values also showed that there was a significant niche overlap between large predators within LVF, which strongly suggests resource competition, this is further supported by the density of large predators and low density of small and medium herbivores.[13]Including supplementary materials

Life restoration ofAmphimachairodus hezhengensis andDinocrocuta, two carnivorans present within the Dashengou Fauna

Within the Dashengou Fauna of the Linxia Basin,Albanosmilus coexisted with a number of large carnivorans such as the largepercrocutid hyenaDinocrocuta gigantea, machairodontsAmphimachairodus hezhengensis andMachairodus aphanistus, and two unnamedagriotheriini bears.Dinocrocuta was the most abundant carnivore found within this fauna found to be the most common carnivoran within this fauna and was likely a top predator within the fauna.Albanosmilus was rather rare, making up 6.2% of the carnivorans present.[21][22] Herbivores within this fauna include rhinoceros such asAcerorhinus hezhengensis,Chilotherium wimani, andIranotherium morgani,suidChleuastochoerusstehlini, cervidDicrocerus, bovidMiotragocerus, giraffidsHonanotheriumschlosseri andSamotherium, and proboscideanTetralophodon exoletus.[23] Due to the abundance of hypercarnivorous cursorial and non-cursorial terrestrial predators, suggests that the Linxia Basin environment was always relatively open.[22]

Extinction

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Albanosmilus jourdani disappeared from theIberian Peninsula around 9.1Ma. Within the Linxia Basin,Albanosmilus went extinct 8.5 Ma, and in North America,A. whitfordi went extinct around 7 Ma.[13][16][7][22] Some have hypothesized that the extinction of barbourofelines, such asAlbanosmilus, was due to competition with sabertooth cats such asMachairodus andNimravides.[24][13] However, this hypothesis has been questioned as their temporal overlap was limited.[6][7] In addition,Albanosmilus was able to successfully coexist with bothAmphimachairodus andMachairodus within Linxia Basin and Los Valles de Fuentidueña.[21][13]

Other experts argue the more likely cause of their extinction was faunal overturns during the Late Miocene.[25][26][7]Albanosmilus’ extinction in the Iberian Peninsula was contemporary with Vallesian-Turolian turnover event, also known as theVallesian Crisis. Which saw an increase of precipitation of seasonality, which gave way for drier, more open environments, suggestingAlbanosmilus wasn’t adapted to the drier, open environments.[13]

References

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  1. ^abWerdelin, Lars (November 2021)."African Barbourofelinae (Mammalia, Nimravidae): a critical review".Historical Biology.34 (2):1347–1355.doi:10.1080/08912963.2021.1998034.
  2. ^abRobles, Josep M.; Alba, David M.; Fortuny, Josep; Esteban-Trivigno, Soledad De; Rotgers, Cheyenn; Balaguer, Jordi; Carmona, Raül; Galindo, Jordi; Almécija, Sergio; Bertó, Juan V.; Moyà-Solà, Salvador (2013). "New craniodental remains of the barbourofelidAlbanosmilus jourdani(Filhol, 1883) from the Miocene of the Vallès-Penedès Basin (NE Iberian Peninsula) and the phylogeny of the Barbourofelini".Journal of Systematic Palaeontology.11 (8):993–1022.Bibcode:2013JSPal..11..993R.doi:10.1080/14772019.2012.724090.S2CID 85157737.
  3. ^Tseng, Z. Jack; Takeuchi, Gary T.; Wang, Xiaoming (January 2010)."Discovery of the Upper Dentitle of Brbourofelis whitfordi (Nimravidae, Carnivora) and an Evaluation of the Genus in California".Journal of Vertebrate Paleontology.30 (1):244–254.doi:10.1080/02724630903416001.
  4. ^Bryant, H. N. (1991). "Phylogenetic relationships and systematics of the Nimravidae (Carnivora)".Journal of Mammalogy.72 (1):56–78.Bibcode:1991JMamm..72...56B.doi:10.2307/1381980.JSTOR 1381980.
  5. ^Wang, Xiaoming; White, Stuart C.; Guan, Jian (2 May 2020)."A new genus and species of sabretooth, Oriensmilus liupanensis (Barbourofelinae, Nimravidae, Carnivora), from the middle Miocene of China suggests barbourofelines are nimravids, not felids".Journal of Systematic Palaeontology.18 (9):783–803.Bibcode:2020JSPal..18..783W.doi:10.1080/14772019.2019.1691066.S2CID 211545222.
  6. ^abBarrett, P. Z.; Hopkins, W. S. B.; Price, S. A. (2021). "How many sabertooths? Reevaluating the number of carnivoran sabertooth lineages with total-evidence Bayesian techniques and a novel origin of the Miocene Nimravidae".Journal of Vertebrate Paleontology.41 (1) e1923523.Bibcode:2021JVPal..41E3523B.doi:10.1080/02724634.2021.1923523.S2CID 236221655.
  7. ^abcdefBarrett, Paul Zachary (26 October 2021)."The largest hoplophonine and a complex new hypothesis of nimravid evolution".Scientific Reports.11 (1) 21078.Bibcode:2021NatSR..1121078B.doi:10.1038/s41598-021-00521-1.PMC 8548586.PMID 34702935.S2CID 240000358.
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  9. ^Jasinski, Steven E.; Abbas, Ghyour; Mahmood, Khalid; et al. (November 2022)."New Carnivoran (Mammalia: Carnivora) specimens from the Siwaliks of Pakistan and India and their faunal and evolutionary implications".Historical Biology.35 (11):2217–2252.doi:10.1080/08912963.2022.2138376.
  10. ^Chabrol, Nils; Morlon, Hélène; Barido-Sottani, Joëlle (July 2025). "The Fossilized Birth Death Process with heterogeneous diversification rates unravels the link between diversification and specialisation to a carnivorous diet in Nimravidae (Carnivoraformes)". pp. 1–26.bioRxiv 10.1101/2025.07.15.664897.
  11. ^Jordy Antón, Mauricio, Agustí; Mauricio, Antón (2002).Mammoths, Sabertooths, And Hominids. Columbia University Press. p. 145.ISBN 0-231-11640-3.
  12. ^Michael Morlo (2006)."New remains of Barbourofelidae from the Miocene of Southern Germany: implications for the history of barbourid migrations".Beiträge zur Paläontologie, Wien.30:339–346.
  13. ^abcdefghDomingo, Laura; Domingo, M. Soledad; Koch, Paul L.; Alberdi, M. Teresa (May 10, 2017)."Carnivoran resource and habitat use in the context of a Late Miocene faunal turnover episode".Palaeontology.60 (4):461–483.Bibcode:2017Palgy..60..461D.doi:10.1111/pala.12296.
  14. ^abcdeGross, Martin; Prieto, Jérôme; Grímsson, Friðgeir; Bojar, Hans-Peter (2023-07-26)."Hyena and 'false' sabre-toothed cat coprolites from the late Middle Miocene of south-eastern Austria".Historical Biology.36 (9):1903–1922.doi:10.1080/08912963.2023.2237979.ISSN 0891-2963.
  15. ^abMorlo, Michael; Gunnell, Gregg F.; Nagel, Doris (2010)."10 - Ecomorphological analysis of carnivore guilds in the Eocene through Miocene of Laurasia".Carnivoran Evolution. Cambridge University Press. pp. 269–310.doi:10.1017/CBO9781139193436.011.ISBN 978-1-139-19343-6.
  16. ^abTseng, Z. Jack; Takeuchi, Gary T.; Wang, Xiaoming (January 2010)."Discovery of the Upper Dentitle of Brbourofelis whitfordi (Nimravidae, Carnivora) and an Evaluation of the Genus in California".Journal of Vertebrate Paleontology.30 (1):244–254.doi:10.1080/02724630903416001.
  17. ^Antón, Mauricio (2013).Sabertooth. Bloomington, Indiana: University of Indiana Press. p. 104.ISBN 978-0-253-01042-1.
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  19. ^Lautenschlager, Stephan; Figueirido, Borja; Cashmore, Daniel D.; Bendel, Eva-Maria; Stubbs, Thomas L. (2020)."Morphological convergence obscures functional diversity in sabre-toothed carnivores".Proceedings of the Royal Society B.287 (1935):1–10.doi:10.1098/rspb.2020.1818.ISSN 1471-2954.PMC 7542828.PMID 32993469.
  20. ^Andersson, Ki; Werdelin, Lars (December 2003)."The evolution of cursorial carnivores in the Tertiary: Implications of elbow-joint morphology".Proceedings of the Royal Society of London. Series B: Biological Sciences.270 (Suppl 2): S163-5.Bibcode:2003PBioS.270.0070A.doi:10.1098/rsbl.2003.0070.PMC 1809930.PMID 14667370.
  21. ^abJiangzuo, Q; Werdelin, L; Sanisidro, O; Yang, Rong; Fu, Jiao; Li, Shijie; Wang, Shiqi; Deng, Tao (April 2023)."Origin of adaptations to openenvironments and social behaviour insabretoothed cats from the northeasternborder of the Tibetan Plateau".Proceedings of the Royal Society B: Biological Sciences.290 (1997):7–8.doi:10.1098/rspb.2023.0019.PMC 10113030.PMID 37072045.S2CID 20230019.
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  23. ^Deng, Tao (2005). "New Discovery of Iranotherium morgani (Perissodactyla, Rhinocerotidae) from the Late Miocene of the Linxia Basin in Gansu, China, and Its Sexual Dimorphism".Journal of Vertebrate Paleontology.25 (2):442–450.doi:10.1671/0272-4634(2005)025[0442:NDOIMP]2.0.CO;2.ISSN 0272-4634.JSTOR 4524457.S2CID 85820005.
  24. ^Antón, Mauricio (2013).Sabertooth. Bloomington, Indiana: University of Indiana Press. p. 90.ISBN 978-0-253-01042-1.
  25. ^Jiangzuo, Qigao; Li, Shijie; Deng, Tao (2022)."Parallelism and lineage replacement of the late Miocene scimitar-toothed cats from the old and New World"(PDF).iScience.25 (12) 105637.Bibcode:2022iSci...25j5637J.doi:10.1016/j.isci.2022.105637.PMC 9730133.PMID 36505925.
  26. ^Michael Morlo (2006)."New remains of Barbourofelidae from the Miocene of Southern Germany: implications for the history of barbourid migrations".Beiträge zur Paläontologie, Wien.30:339–346.
Afrosmilini
Barbourofelini
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Albanosmilus
Albanosmilus jourdani
Barbourofelis whitfordi
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