Albanosmilus

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Albanosmilus
Temporal range: Middle-Late Miocene (Serravallian to Messinian), 12–7 Ma
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Cranium of Albanosmilus jourdani
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Suborder: Feliformia
Family: †Barbourofelidae
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 extinct genus of the subfamily Barbourofelinae, which has been suggested to be part of the family Nimravidae.[1] The genus currently consists of two named species: Albanosmilus jourdani and Albanosmilus whitfordi. Albanosmilus lived in Eurasia and North America from the Middle to Late Miocene from 12 to 7 mya, making it one of the last nimravids.[2][3] The genus may have been ancestral to Barbourofelis.

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 a jaguar and smaller than Barbourofelis. Like Barbourofelis, A. jourdani was believed to have been an ambulatory, ambush predator and was likely an apex predator of its ecosystem. A. whitfordi was endemic to North America and was smaller in size, more similar in size a leopard. Unlike A. jourdani, A. whitfordi was believed to have been a cursorial predator. In addition, Albanosmilus was also recovered in East Asia.

Taxonomy

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Classification

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Bryant in his 1991 considered Albanosmilus as a member of the false sabre-toothed cat family Nimravidae.[4] However, Albanosmilus was eventually considered part of the Barbourofelidae, where it was considered synonymous to Sansanosmilus. By 2013, this was refuted as the authors argued it had features that differed from Sansanosmilus such as larger size, more reduced p3, and displaying a double fused or single root. It also had features differed from Barbourofelis including the presence of a mesial cingulum cusp in P3 and lack of metaconid in m1. In the addition, the authors also moved Barbourofelis whitfordi to the genus Albanosmilus.[2]

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

Evolution

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According to recent phylogenetic analysis, Barbourofelins likely evolved when Nimravinae taxa migrated into Africa at MN2. Their size was likely constrained due to the diversity of hyaenodonts that roamed Africa. However, they were 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 replaced Sansanosmilus in Europe.[10]

A. jourdani may have migrated into North America and evolved into the genus Barbourofelis and the species A. whitfordi.[11]

Description

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Albanosmilus jourdani is estimated to have weighed around 80–100 kg (180–220 lb),[12][13] one estimate suggests this species could’ve even exceeded 100 kg (220 lb).[14] Making it one of the largest barbourofelid, just behind Barbourofelis. A. whitfordi was considered to be similar in size to B. morrisi, which was as large as a leopard.[15][16]

Paleobiology

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Albanosmilus is speculated to either have been a pack or solitary hunter.[12][13] A 2020 study estimated that A. jourdani had a jaw gape of 90 degrees.[17] Including supplementary materials Coprolites likely referable to this genus were described in 2023, which may suggest that Albanosmilus 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 of Albanosmilus largely consisted of meat, which is consistent with its hypercarnviorous dentition and presumed nutrients.[13] While A. jourdani was recovered as an ambush, ambulatory predator,[13][14] A. whitfordi has been recovered as a cursorial predator based on elbow morphology.[18]

Paleoecology

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Albanosmilus jourdani was found in Eurasia, and lived from 11.9-9.1 Ma.[12][7] Including supplementary materials This species was found in Gratkorn, it coexisted with herbivores such as would include equid Anchitherium, suids such as Parachleuastochoerus steinheimensis and listriodontinae Listriodon splendens, palaeomerycidae Palaeomeryx, chalicotheriidae Chalicotherium, aceratheriinae rhinos Aceratherium, Brachypotherium and Lartetotherium, and deinotheriinae proboscidean Deinotherium. The contemporary carnivoran within this locality was the hyena Protictitherium, both carnivores would’ve coexisted by hunting prey of different sizes. Based on the coprolites, equid, suids, and palaeomerycids were probable prey for Albanosmilus. While on the other hand, chalicotheres, rhinos, and proboscideans were would’ve been improbable prey, with social hunting comparable to lion prides being required to hunt young proboscideans. On the other hand, there is possible evidence of Albanosmilus scavenging on Deinotherium.[13]

Within Los Valles de Fuentidueña, A. jourdani coexisted with carnivorans including Felids such as the basal Pseudaelurus quadridentatus and machairodont Machairodus aphanistus, amphicyoninae Magericyon castellanus, and ictitheriinae hyena Lycyaena chaeretis. Herbivores within this locality include hipparionini equid Hippotherium primigenium, aceratheriinae rhinos Aceratherium incisivum and Alicornops simorrense, bovid Miotragocerus, cervid Euprox dicranocerus, tragulid Dorcatherium naui, giraffid Decennatherium pachecoi, and "tetralophodont gomphothere" Tetralophodon longirostris. Isotopic analysis shows Albanosmilus hunted in woodland to mesic grasslands and preyed upon Hippotherium, Miotragocerus, Euprox, Dorcatherium, and Chalicomys. Miotragocerus was found to make the greatest contribution to its diet while Dorcatherium 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.[12] Including supplementary materials

Within the Dashengou Fauna of the Linxia Basin, Albanosmilus coexisted with a number of large carnivorans such as the large percrocutid hyena Dinocrocuta gigantea, machairodonts Amphimachairodus hezhengensis and Machairodus aphanistus, and two unnamed agriotheriini 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.[19][20] Herbivores within this fauna include rhinoceros such as Acerorhinus hezhengensis, Chilotherium wimani, and Iranotherium morgani, suid Chleuastochoerus stehlini, cervid Dicrocerus, bovid Miotragocerus, giraffids Honanotherium schlosseri and Samotherium, and proboscidean Tetralophodon exoletus.[21] Due to the abundance of hypercarnivorous and non-cursorial and cursorial terrestrial predators, which suggests that the Linxia Basin environment was always relatively open.[20]

Extinction

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Albanosmilus jourdani disappeared from the Iberian Peninsula around 9.1 Ma. Within the Linxia Basin, Albanosmilus went extinct 8.5 Ma, and in North America, A. whitfordi went extinct around 7 Ma. [12][15][7][20] Some have hypothesized that the extinction of barbourofelids, such as Albanosmilus, was due to competition with sabertooth cats such as Machairodus and Nimravides.[22][12] However, this hypothesis has been questioned as their temporal overlap was limited.[6][7] In addition, Albanosmilus was able to successfully coexist with both Amphimachairodus and Machairodus within Linxia Basin and Los Valles de Fuentidueña.[19][12]

Other experts argue the more likely cause of their extinction was faunal overturns during the Late Miocene.[23][24][7]

References

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  1. ^ a b Werdelin, Lars (November 2021). "African Barbourofelinae (Mammalia, Nimravidae): a critical review". Historical Biology. 34 (2): 1–9. doi:10.1080/08912963.2021.1998034.
  2. ^ a b Robles, 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 barbourofelid Albanosmilus 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. 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. 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. doi:10.1080/14772019.2019.1691066. S2CID 211545222.
  6. ^ a b Barrett, 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. doi:10.1080/02724634.2021.1923523. S2CID 236221655.
  7. ^ a b c d e f Barrett, 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.
  8. ^ Barret, Paul Z.; Hopkins, Samatha S. B. (2024). "Mosaic evolution underlies feliform morphological disparity". Proc. R. Soc. B. 291 (2028).
  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): 1–35. doi:10.1080/08912963.2022.2138376.
  10. ^ Jordy Antón, Mauricio, Agustí; Mauricio, Antón (2002). Mammoths, Sabertooths, And Hominids. Columbia University Press. p. 145. ISBN 0-231-11640-3.
  11. ^ 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.
  12. ^ a b c d e f g Domingo, 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. doi:10.1111/pala.12296.
  13. ^ a b c d e Gross, 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: 1–20. doi:10.1080/08912963.2023.2237979. ISSN 0891-2963.
  14. ^ a b Morlo, 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 9781139193436.
  15. ^ a b 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.
  16. ^ Antón, Mauricio (2013). Sabertooth. Bloomington, Indiana: University of Indiana Press. p. 104. ISBN 9780253010421.
  17. ^ 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.
  18. ^ Andersson, Ki; Werdelin, Lars (December 2003). "The evolution of cursorial carnivores in the Tertiary: Implications of elbow-joint morphology". Proceeding of the Royal Society B. 270. doi:10.1098/rsbl.2003.0070.
  19. ^ a b Jiangzuo, 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.
  20. ^ a b c Jiangzuo, Qigao; Wang, Shiqi; Deng, Tao (1 April 2023). "Chronological framework and palaeoecology of Carnivora from the Linxia Basin, China". Palaeogeography, Palaeoclimatology, Palaeoecology. 615.
  21. ^ 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.
  22. ^ Antón, Mauricio (2013). Sabertooth. Bloomington, Indiana: University of Indiana Press. p. 90. ISBN 9780253010421.
  23. ^ 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.
  24. ^ 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.