2020 in reptile paleontology

This list of fossil reptiles described in 2020 is a list of new taxa of fossil reptiles that were described during the year 2020, as well as other significant discoveries and events related to reptile paleontology that occurred in 2020.

List of years in reptile paleontology
  • 2010
  • 2011
  • 2012
  • 2013
  • 2014
  • 2015
  • 2016
  • 2017
  • 2018
  • 2019
  • 2020
  • 2021
  • 2022
  • 2023
  • 2024
  • 2025
  • 2026
  • 2027
  • 2028
  • 2029
  • 2030
In archosaur paleontology
2017
2018
2019
2020
2021
2022
2023

Lizards and snakes

New taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Bothriagenys flectomendax[1] Sp. nov In press Wick & Shiller Late Cretaceous (early Campanian) Aguja  United States
( Texas)
A member of Borioteiioidea of uncertain phylogenetic placement.
Calumma benovskyi[2] Sp. nov Čerňanský et al. Early Miocene Hiwegi  Kenya A chameleon, a species of Calumma
Chalcides augei[3] Sp. nov Valid Čerňanský et al. Early middle Miocene  Russia A skink, a species of Chalcides. Announced in 2019; the final version of the article naming it was published in 2020.
Eoconstrictor[4] Gen. et comb. nov Valid Scanferla & Smith Eocene Messel  Germany A booid snake. The type species is "Palaeopython" fischeri Schaal (2004).
Epileolis[5] Gen. et sp. nov Valid Alifanov Late Paleocene  Mongolia A lizard belonging to the family Agamidae. Genus includes new species E. reshetovi.
Hydrargysaurus[1] Gen. et sp. nov In press Wick & Shiller Late Cretaceous (early Campanian) Aguja  United States
( Texas)
A member or a relative of the group Borioteiioidea. Genus includes new species H. gladius.
Hypostylos[1] Gen. et sp. nov In press Wick & Shiller Late Cretaceous (early Campanian) Aguja  United States
( Texas)
A member of Scincomorpha belonging to the "paramacellodid"/cordylid grade. Genus includes new species H. lehmani.
Neokotus[6] Gen. et sp. nov Valid Bittencourt et al. Early Cretaceous (Valanginian) Quiricó  Brazil A lizard belonging to the family Paramacellodidae. The type species is N. sanfranciscanus.

Research

  • New fossil material of squamates is described from the Upper Cretaceous Fruitland and Kirtland formations (New Mexico, United States) by Woolley, Smith & Sertich (2020), expanding known taxonomic and morphological diversity of lizards within the "Hunter Wash Local Fauna".[7]
  • A study on the affinities of putative gekkotan eggshells from the Late Cretaceous of Europe is published by Choi et al. (2020), who interpret the fossil material of Pseudogeckoolithus as theropod eggshells.[8]
  • Fossils of tupinambine teiids are described from the late Eocene of the Quercy Phosphorites Formation (France) by Louis & Santiago (2020), representing the first record of this family from the Paleogene of Europe.[9]
  • A dentary of a cnemidophorine teiid is described from the Miocene of the Ogallala Group (Nebraska, United States) by Scarpetta (2020), who evaluates the implications of this specimen for the knowledge of the evolutionary history of cnemidophorines in North America during the Neogene.[10]
  • Fossil material of the monitor lizards is reported for the first time from the late Miocene localities in Armenia and Georgia by Vasilyan & Bukhsianidze (2020).[11]
  • A study on the evolutionary history of mosasauroids, comparing their evolutionary rates and traits to those of plesiosaurs and aiming to determine whether the rise and diversification of mosasauroids was influenced by competition with or disappearance of some plesiosaur taxa, is published by Madzia & Cau (2020).[12]
  • Grigoriev & Grabovskiy (2020) describe new fossil material of a tylosaurine from the Upper Cretaceous (Turonian) of the Chukotka Region (Russia), representing one of the oldest and northernmost mosasaur records reported so far, and evaluate the implications of this fossil material (as well as mosasaur fossils from the Santonian of the Komi Republic and from the CampanianMaastrichtian of the Sakhalin Island) for the knowledge of the paleogeography and possible migrations of Arctic mosasaurs.[13]
  • A study on pathological features of a specimen of Prognathodon (belonging or related to the species P. sectorius) from the Maastrichtian Gulpen Formation (the Netherlands) is published by Bastiaans et al. (2020), who consider it most likely that this specimen was bitten in the snout by a large, possibly conspecific mosasaur, making it one of the few specimens with unambiguous evidence of agonistic interactions amongst mosasaurs.[14]
  • A study on the morphology of the snout of Taniwhasaurus antarcticus, indicating the presence of a complex internal neurovascular system of branched channels similar to systems present in extant aquatic vertebrates such as cetaceans and crocodiles, is published by Álvarez–Herrera, Agnolin & Novas (2020).[15]
  • Redescription of Palaeophis oweni is published by Georgalis, Del Favero & Delfino (2020).[16]
  • Description of new fossil material of Thaumastophis missiaeni from the Eocene Cambay Shale Formation (India) and a study on the phylogenetic relationships of this snake is published by Zaher et al. (2020), who name a new family Thaumastophiidae.[17]

Ichthyosauromorphs

New taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Acuetzpalin[18] Gen. et sp. nov Valid Barrientos Lara, Alvarado Ortega, & Fernández Late Jurassic La Casita  Mexico An ichthyosaur belonging to the family Ophthalmosauridae. The type species is A. carranzai.
Cymbospondylus duelferi[19] Sp. nov Valid Klein et al. Middle Triassic (Anisian) Favret  United States
( Nevada)
Hauffiopteryx altera[20] Sp. nov Valid Maxwell & Cortés Early Jurassic (Toarcian) Posidonia Shale  Germany
Nannopterygius borealis[21] Sp. nov Valid Zverkov & Jacobs Early Cretaceous (Berriasian)  Norway
 Russia

Research

  • Partial trunk region of the largest hupehsuchian reported so far is described from the Early Triassic of Hubei, China by Qiao, Iijima & Liu (2020), who interpret this specimen as evidence of early establishment of high predation pressure in the sea after the Permian–Triassic extinction event and before the Middle Triassic.[22]
  • New anatomical features of the holotype specimen of Cartorhynchus lenticarpus revealed by CT scanning, including unique dentition, are reported by Huang et al. (2020), who evaluate the implications of this species for the knowledge of the evolution of tooth morphology and diet in basal ichthyosauriforms.[23]
  • A study on the tempo and mode of the morphological evolution of ichthyosaurs is published by Moon & Stubbs (2020).[24]
  • A study on skeletal pathologies in ichthyosaur specimens from the Middle Triassic Besano Formation and the Lower Jurassic Posidonia Shale, evaluating their implications for the knowledge of changing locomotory and behavioural constraints affecting different ichthyosaur taxa through time, is published by Pardo-Pérez, Kear & Maxwell (2020).[25]
  • Two new specimens of Mixosaurus cornalianus, preserving evidence of the presence of a dorsal fin and a well-developed, triangular dorsal lobe of the caudal fin in this species, are described from the Anisian Besano Formation (Italy) by Renesto et al. (2020).[26]
  • Description of the most complete and best-preserved skeleton of Suevoleviathan integer is published by Maisch (2020).[27]
  • Partial skeleton of an ophthalmosaurid ichthyosaur, found with an ichthyosaur tooth (probably not belonging to the same specimen) stuck on its rib, is described from the Upper Jurassic Rosso Ammonitico Veronese Formation (Italy) by Serafini et al. (2020), possibly representing the first evidence of scavenging between two ichthyosaurs reported so far.[28]
  • A study on the anatomy and phylogenetic relationships of Maiaspondylus lindoei, "Ophthalmosaurus" cantabrigiensis and "Platypterygius" ochevi is published by Zverkov & Grigoriev (2020), who transfer "O". cantabrigiensis to the genus Maiaspondylus, and consider "P. ochevi to be a junior synonym of M. cantabrigiensis.[29]

Sauropterygians

New taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Ophthalmothule[30] Gen. et sp. nov Valid Roberts et al. Jurassic-Cretaceous boundary (latest Tithonian/early Berriasian) Agardhfjellet  Norway A cryptoclidid plesiosaur. The type species is O. cryostea.

Research

  • A study on the osteology and evolution of the temporal region of the skull of placodonts is published by Maisch et al. (2020).[31]
  • New fossil material of Lariosaurus sanxiaensis is described from the Lower Triassic Jialingjiang Formation (China) by Li & Liu (2020), who also study the phylogenetic relationships of this taxon, as well as the predator-prey relationship in the associated fauna and their implications for the knowledge of the biotic recovery after the Permian–Triassic extinction event.[32]
  • New fossil material of cryptoclidid plesiosaurs, including the first occurrence of Vinialesaurus in the Southern Hemisphere, is described from the Jurassic of the Atacama Desert by Otero et al. (2020).[33]
  • Redescription of the holotype specimen of Aphrosaurus furlongi and a study on the evolution and phylogenetic relationships of elasmosaurid plesiosaurs is published by O’Gorman (2020), who names a new clade Euelasmosaurida.[34]
  • An isolated cervical centrum of a brachauchenine pliosaurid is described from the Cenomanian of Russia by Zverkov & Pervushov (2020), who interpret this fossil as belonging to one of the largest known pliosaurids, and consider it to be evidence of survival gigantic pliosaurids into the Cenomanian.[35]

Turtles

New taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Alatochelon[36] Gen. et sp. nov Valid Pérez-García, Vlachos & Murelaga Early Pliocene Cigarrón  Spain A large tortoise. Genus includes new species A. myrteum.
Amabilis[37] Gen. et sp. nov Valid Hermanson et al. Late Cretaceous Bauru  Brazil A podocnemidoid pleurodiran. Genus includes new species A. uchoensis.
Aragochersis[38] Gen. et sp. nov In press Pérez García et al. Early Cretaceous (Albian) Escucha  Spain A member of the family Helochelydridae. Genus includes new species A. lignitesta.
Chelonoidis alburyorum keegani[39] Subsp. nov Valid Franz, Albury & Steadman Late Holocene  Turks and Caicos Islands A tortoise.
Chelonoidis alburyorum sementis[39] Subsp. nov Valid Franz, Albury & Steadman Late Holocene  Turks and Caicos Islands A tortoise.
Jainemys[40] Gen. et comb. nov Valid Joyce & Bandyopadhyay Late Cretaceous (Maastrichtian) Lameta  India A member of the family Bothremydidae belonging to the tribe Kurmademydini; a new genus for "Carteremys" pisdurensis Jain (1977).
Lakotemys[41] Gen. et sp. nov Valid Joyce, Rollot & Murelaga Early Cretaceous (BerriasianValanginian) Lakota  United States
( South Dakota)
A member of the family Baenidae. The type species is L. australodakotensis.
Laurasichersis[42] Gen. et sp. nov Pérez García Paleocene (Thanetian) Sables de Bracheux  France A member of the family Sichuanchelyidae. The type species is L. relicta.
Melanochelys tapani[43] Nom. nov Valid Garbin, Bandyopadhyay & Joyce Miocene/Pliocene Siwalik Hills  India A species of Melanochelys; a replacement name for Nicoria tricarinata var. sivalensis Lydekker (1889).
Mesoclemmys vanegasorum[44] Sp. nov Valid Cadena et al. Laventan La Victoria  Colombia A species of Mesoclemmys
Prochelidella buitreraensis[45] Sp. nov Valid Maniel et al. Late Cretaceous (Cenomanian) Candeleros  Argentina
Testudo hellenica[46] Sp. nov Valid Garcia et al. Miocene (Vallesian)  Greece A species of Testudo.
Waluchelys[47] Gen. et sp. nov Valid Sterli et al. Late Triassic  Argentina A member of the family Australochelyidae. Genus includes new species W. cavitesta.
Yaminuechelys sulcipeculiaris[48] Sp. nov In press Oriozabala, Sterli & De La Fuente Late Cretaceous (CampanianMaastrichtian) La Colonia  Argentina A member of the family Chelidae

Research

  • A study on the evolution of turtle skull architecture, aiming to assess the functional significance of changes in their skull architecture during feeding on the basis of data from extant and fossil taxa, is published by Ferreira et al. (2020).[49]
  • A study on non‐marine turtle distribution and diversity from the Late Triassic to the Paleogene is published by Cleary et al. (2020).[50]
  • Description of new fossil material of Indochelys spatulata from the Jurassic Kota Formation (India), and a study on the anatomy and phylogenetic relationships of this taxon, is published by Joyce & Bandyopadhyay (2020).[51]
  • Cadena et al. (2020) describe new fossil material of Stupendemys geographicus from the Miocene of Venezuela and Colombia, providing new information on the anatomy and paleobiology of this species.[52]
  • Peltochelys duchastelii is reinterpreted as a member of Paracryptodira by Joyce & Rollot (2020).[53]
  • Description of the anatomy of the skull of Pleurosternon bullockii is published by Evers, Rollot & Joyce (2020).[54]
  • Redescription of the anatomy of the skull and mandible of Sandownia harrisi is published by Evers & Joyce (2020).[55]
  • A revision of the extinct geoemydid Echmatemys from North America, based mainly on data from a slab containing several turtle shells collected from the Bridgerian of Levett Creek (Wyoming, United States), is published by Vlachos (2020).[56]
  • A study on the phylogenetic relationships of a putative testudinoid Cardichelyon rogerwoodi is published by Joyce & Claude (2020), who consider it more likely that this taxon is a member of Kinosternoidea.[57]

Archosauriformes

Archosaurs

Other archosauriforms

New taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Polymorphodon[58] Gen. et sp. nov In press Sues et al. Middle Triassic (Ladinian) Erfurt  Germany A non-archosaurian member of Archosauriformes. Genus includes new species P. adorfi.
Rugarhynchos[59] Gen. et comb. nov Valid Wynd et al. Late Triassic Chinle  United States
( New Mexico)
A member of the family Doswelliidae; a new genus for "Doswellia" sixmilensis Heckert, Lucas & Spielmann (2012).

Research

  • Redescription of the anatomy of the holotype specimen of Chanaresuchus bonapartei and a study on the phylogenetic relationships of this species is published by Trotteyn & Ezcurra (2020).[60]
  • Redescription of the anatomy of the skull and mandible of Euparkeria capensis is published Sookias et al. (2020).[61]
  • Phytosaur remains are described from the Upper Triassic Upper Karoo Group (Zimbabwe) by Barrett et al. (2020), representing the first record of members of this group from sub-Saharan Africa.[62]
  • An assemblage of at least 21 phytosaur specimens dominated by juveniles and subadults is described from the Upper Triassic Tiki Formation (India) by Datta, Mukherjee & Ray (2020), who interpret this finding as likely evidence of parental care in phytosaurs, and study the taphonomy of the assemblage.[63]

Other reptiles

New taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Carbonodraco Gen. et sp. nov Valid Mann et al. Carboniferous (Moscovian) Allegheny  United States A member of the family Acleistorhinidae. The type species is C. lundi. Announced in 2019;[64] the correction including the required ZooBank accession number was published in 2020.[65]
Elessaurus[66] Gen. et sp. nov Valid De-Oliveira et al. Early Triassic Sanga do Cabral  Brazil An archosauromorph reptile of uncertain phylogenetic placement, possibly a relative of tanystropheids. The type species is E. gondwanoccidens.

Gunakadeit[67] Gen. et sp. nov Valid Druckenmiller et al. Late Triassic (Norian) Hound Island  United States
( Alaska)
A thalattosaur. The type species is G. joseeae.
Heishanosaurus[68] Gen. et sp. nov Valid Dong et al. Early Cretaceous (AptianAlbian) Shahai  China A member of Choristodera. The type species is H. pygmaeus.
Lanceirosphenodon[69] Gen. et sp. nov Valid Vivar et al. Late Triassic (Norian) Candelária  Brazil A rhynchocephalian. Genus includes new species L. ferigoloi.
Oryctorhynchus[70] Gen. et sp. nov Valid Sues, Fitch & Brochu Late Triassic (Carnian? - Norian?) Wolfville  Canada
( Nova Scotia)
A rhynchosaur. Genus includes new species O. bairdi.
Raibliania[71] Gen. et sp. nov Valid Dalla Vecchia Late Triassic (Carnian) Calcare del Predil  Italy A member of the family Tanystropheidae. The type species is R. calligarisi.
Smilodonterpeton[72] Gen. et sp. nov In press Skinner, Whiteside & Benton Late Triassic (Rhaetian)  United Kingdom A procolophonid. Genus includes new species S. ruthinensis.
Tanystropheus hydroides[73] Sp. nov Valid Spiekman et al. Late Triassic Besano Italy-Switzerland border
Trilophosaurus phasmalophos[74] Sp. nov Valid Kligman et al. Late Triassic (Norian) Chinle  United States
( Arizona)

Vellbergia[75] Gen. et sp. nov Sobral, Simões & Schoch Middle Triassic (Ladinian) Erfurt  Germany A non-lepidosaurian lepidosauromorph. The type species is V. bartholomaei.

Research

  • A study on fracture planes (unossified regions in the middle of vertebral centra) in tail vertebrae of mesosaurs is published by MacDougall et al. (2020), who argue that mesosaurs were theoretically capable of tail autotomy, but probably did not utilize this ability.[76]
  • A study on patterns of tooth development and replacement in Belebey and Bolosaurus, indicating that bolosaurid teeth had thecodont implantation with deep roots, is published by Snyder et al. (2020).[77]
  • A study on the dental wear along the tooth rows of nearly one hundred jaws of Captorhinus aguti, indicating that this reptile preferred to feed using the right side of the jaw, is published by Reisz et al. (2020).[78]
  • A study on the feeding mechanics and ecology of Clevosaurus hudsoni and C. cambrica, as indicated by their bite force, resistance of skull bones to bending and torsion, and the distribution of stresses in the jaws during biting, is published by Chambi‐Trowell et al. (2020).[79]
  • A study on the anatomy and phylogenetic relationships of Colobops noviportensis is published by Scheyer et al. (2020), who reinterpret this taxon as a probable rhynchocephalian.[80]
  • A study on the morphology of teeth of Priosphenodon avelasi is published by LeBlanc et al. (2020).[81]
  • Partial skeleton of a small reptile, probably a juvenile specimen of Eusaurosphargis dalsassoi, is described from the Anisian Buchenstein Formation (northern Dolomites, Italy) by Renesto, Kustatscher & Gianolla (2020), who interpret this finding as possible evidence of that the lands emerged near the basins of the northern Dolomites, Besano Formation and Prosanto Formation had a similar reptilian fauna during the middle-late Anisian.[82]
  • A study on the anatomy of the skull of Champsosaurus lindoei is published by Dudgeon et al. (2020), who evaluate the morphology of a putative neomorphic bone in the skull and its possible developmental and functional origins.[83]
  • A study on the internal anatomy of the skull of Champsosaurus lindoei and C. natator, and on their probable sensory abilities, is published by Dudgeon et al. (2020).[84]
  • Redescription of the anatomy of the skeleton of Macrocnemus fuyuanensis is published by Scheyer et al. (2020).[85]
  • Description of the morphology of the skull of Macrocnemus bassanii is published by Miedema et al. (2020).[86]
  • A study on bone histology of three archosauromorph reptiles (Lagerpeton chanarensis, Tropidosuchus romeri and Chanaresuchus bonapartei) from the Triassic Chañares Formation (Argentina), evaluating its implications for the knowledge of the paleobiology of these taxa, is published by Marsà, Agnolín & Novas (2020).[87]

Reptiles in general

  • A study on the dynamics of phenotypic and molecular evolution of reptiles during the early diversification of the major lineages of diapsid reptiles in the Permian and Triassic periods, and during the evolution of lepidosaurs from the Jurassic to the present, is published by Simões et al. (2020).[88]
  • A large, soft-shelled egg, most closely resembling eggs of extant lizards and snakes and possibly produced by a mosasaur, is described from the Upper Cretaceous Lopez de Bertodano Formation (Antarctica) by Legendre et al. (2020), who name a new ootaxon Antarcticoolithus bradyi.[89]
  • A study on the evolution of the archosauromorph ankle, aiming to test the hypothesis of fusion between the centrale and astragalus and the alternative hypothesis of a complete loss of the centrale, based on embryological and palaeontological data, is published by Blanco, Ezcurra & Bona (2020).[90]

References

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