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Thadeosaurus

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Thadeosaurus
Temporal range: Late Permian, ?CapitanianLopingian
Speculative life restoration
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Diapsida
Clade: Neodiapsida
Family: Younginidae
Genus: Thadeosaurus
Carroll, 1981
Type species
Thadeosaurus colcanapi
Carroll, 1981

Thadeosaurus is an extinct genus of diapsid reptiles from the late Permian Lower Sakamena Formation (Sakamena Group) of Madagascar. The genus contains a single species, Thadeosaurus colcanapi, known from several specimens preserved as natural molds.

Discovery and naming

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The generic name, Thadeosaurus, is an anagram of "Datheosaurus", a synapsid genus to which fossils of the former were initially referred. The specific name, colcanapi, honors J.-M. Colcanap, a French infantry captain and the discoverer of the holotype specimen.[1][2]

Description

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Size compared to a human hand

Thadeosaurus was a superficially lizard-like reptile, with a remarkably long tail that comprised about two-thirds of the animal's total length of 60 centimetres (24 in). It had long toes, especially on the hind legs, and a strong breast bone.[1][3][2]

Classification

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The relationships of Thadeosaurus have been debated since its 1981 description. Prior to receiving a name, the fossil material was provisionally referred to Broomia (now recognized as a millerettid[4]), Tangasaurus, and Datheosaurus (now recognized as a caseid synapsid). In his 1981 publication naming Thadeosaurus and Claudiosaurus, Carroll noted similarities between Thadeosaurus and Youngina, but opted to describe it as a 'primitive' sauropterygian—an 'ancestral taxon' to nothosaurs and plesiosaurs.[1]

In the description of the early Permian reptile Orovenator, the phylogenetic results of Reisz et al. (2011) suggested a close relationship between Thadeosaurus and Youngina, united in the family Younginidae. These results are displayed in the cladogram below:[5]

In 2025, Valentin Buffa and colleagues thoroughly redescribed the fossil material assigned to Thadeosaurus, and reassessed its phylogenetic position. They identified it as a member of the neodiapsid family Tangasauridae, as the sister taxon to the clade formed by Hovasaurus and Tangasaurus, a position also supported by Philip J. Currie in a publication redescribing Tangasaurus.[6] The results of the strict consensus phylogenetic results of Buffa et al. (2025) are displayed in the cladogram below:[2]

References

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  1. ^ a b c Carroll, Robert L. (1981). "Plesiosaur ancestors from the Upper Permian of Madagascar". Philosophical Transactions of the Royal Society. B. 293 (1066): 315–383. Bibcode:1981RSPTB.293..315C. doi:10.1098/rstb.1981.0079.
  2. ^ a b c Buffa, Valentin; Jalil, Nour‐Eddine; Falconnet, Jocelyn; Vincent, Peggy (2025-03-23). "The neodiapsid Thadeosaurus colcanapi from the upper Permian of Madagascar". Papers in Palaeontology. 11 (2). doi:10.1002/spp2.70008. ISSN 2056-2799.
  3. ^ Currie, Philip J.; Carroll, Robert L. (September 1984). "Ontogenetic changes in the eosuchian reptile Thadeosaurus". Journal of Vertebrate Paleontology. 4 (1): 68–84. doi:10.1080/02724634.1984.10011987. ISSN 0272-4634.
  4. ^ Jenkins, Xavier A; Benson, Roger B J; Elliott, Maya; Jeppson, Gabriel; Dollman, Kathleen; Fernandez, Vincent; Browning, Claire; Ford, David P; Choiniere, Jonah; Peecook, Brandon R (2025-03-03). "New information on the anatomically derived millerettid Milleretta rubidgei from the latest Permian based on µCT data". Zoological Journal of the Linnean Society. 203 (3). doi:10.1093/zoolinnean/zlaf004. ISSN 0024-4082.
  5. ^ Robert R. Reisz; Sean P. Modesto; Diane M. Scott (2011). "A new Early Permian reptile and its significance in early diapsid evolution". Proceedings of the Royal Society B. 278 (1725): 3731–3737. doi:10.1098/rspb.2011.0439. PMC 3203498. PMID 21525061.
  6. ^ Currie, P. J.; Currie, P. J. (1982). "The osteology and relationships of Tangasaurus mennelli Haughton". Annals of the South African Museum. Annale van die Suid-Afrikaanse Museum. 86: 247–265.