2024 in archosaur paleontology

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List of years in archosaur paleontology
In reptile paleontology
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2024
2025
2026
2027
In paleontology
2021
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2024
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This article records new taxa of every kind of fossil archosaur that are scheduled to be described during 2024, as well as other significant discoveries and events related to the paleontology of archosaurs that will be published in 2024.

Contents

Pseudosuchians

New pseudosuchian taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages

Aphaurosuchus kaiju [1]

Sp. nov

In press

Martins et al.

Late Cretaceous

Adamantina Formation

Flag of Brazil.svg  Brazil

A baurusuchid. Announced in 2023; the final article version was published in 2024.

Asiatosuchus oenotriensis [2]

Sp. nov

Narváez et al.

Eocene (Lutetian)

Flag of Spain.svg  Spain

A basal member of Crocodyloidea.

Benggwigwishingasuchus [3] Gen. et sp. novValidSmith et al.Middle Triassic (Anisian) Favret Formation Flag of the United States.svg  United States
(Flag of Nevada.svg  Nevada)
A member of Paracrocodylomorpha, probably belonging to the group Poposauroidea. The type species is B. eremicarminis. Benggwigwishingasuchus.jpg

Caipirasuchus catanduvensis [4]

Sp. nov

Iori et al.

Late Cretaceous

Adamantina Formation

Flag of Brazil.svg  Brazil

Enalioetes [5]

Gen. et sp. nov

Valid

Sachs et al.

Early Cretaceous (Valanginian)

Stadthagen Formation

Flag of Germany.svg  Germany

A metriorhynchid. The type species is E. schroederi.

Garzapelta [6]

Gen. et sp. nov

Valid

Reyes, Martz & Small

Late Triassic (Norian)

Cooper Canyon Formation

Flag of the United States.svg  United States
(Flag of Texas.svg  Texas)

An aetosaur. The type species is G. muelleri.

Ophiussasuchus [7]

Gen. et sp. nov

Valid

López-Rojas et al.

Late Jurassic (Kimmeridgian-Tithonian)

Lourinhã Formation

Flag of Portugal.svg  Portugal

A goniopholidid crocodylomorph. The type species is O. paimogonectes.

Parvosuchus [8] Gen. et sp. novMüllerTriassic (Ladinian-Carnian)Pinheiros-Chiniquá Sequence of the Santa Maria SupersequenceFlag of Brazil.svg  Brazil A gracilisuchid pseudosuchian. The type species is P. aurelioi. Parvosuchus skull.png

Schultzsuchus [9]

Gen. et comb. nov

Desojo & Rauhut

Triassic (Ladinian-Carnian)

Pinheiros-Chiniquá Sequence of the Santa Maria Supersequence

Flag of Brazil.svg  Brazil

A member of Paracrocodylomorpha, probably belonging to the group Poposauroidea. The type species is "Prestosuchus" loricatus von Huene (1938).

Varanosuchus [10]

Gen et sp. nov

In press

Pochat-Cottilloux et al.

Early Cretaceous

Sao Khua Formation

Flag of Thailand.svg  Thailand

An atoposaurid. The type species is V. sakonnakhonensis.

General pseudosuchian research

Aetosaur research

Crocodylomorph research

Non-avian dinosaurs

New dinosaur taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages

Baiyinosaurus [34]

Gen. et sp. nov

Valid

Ning et al.

Middle Jurassic (Bathonian)

Wangjiashan Formation

Flag of the People's Republic of China.svg  China

A basal stegosaurian. The type species is B. baojiensis.

Baiyinosaurus baojiensis.png

Chakisaurus [35]

Gen. et sp. nov

Alvarez Nogueira et al.

Late Cretaceous (Cenomanian-Turonian)

Huincul Formation

Flag of Argentina.svg  Argentina

An elasmarian ornithopod. The type species is C. nekul.

Chakisaurus UDL.png
Comptonatus [36] Gen. et sp. novLockwood et al.Early Cretaceous (Barremian) Wessex Formation Flag of the United Kingdom.svg  United Kingdom An iguanodontid ornithopod. The type species is C. chasei. Comptonatus chasei.png

Datai [37]

Gen. et sp. nov

Valid

Xing et al.

Late Cretaceous (Turonian-Early Coniacian)

Zhoutian Formation

Flag of the People's Republic of China.svg  China

An ankylosaurid. The type species is D. yingliangis.

Datai (type specimen block).jpg

Diuqin [38]

Gen. et sp. nov

Valid

Porfiri et al.

Late Cretaceous (Santonian)

Bajo de la Carpa Formation

Flag of Argentina.svg  Argentina

A unenlagiine theropod. The type species is D. lechiguanae.

Diuqin humerus (MUCPv 1401-4).png

Dornraptor [39]

Gen. et sp. nov

Valid

Baron

Early Jurassic (Hettangian–Sinemurian)

Blue Lias Formation

Flag of the United Kingdom.svg  United Kingdom

An averostran theropod. The type species is D. normani.

Merosaurus.jpg

Eoneophron [40]

Gen. et sp. nov

Atkins-Weltman et al.

Late Cretaceous (Maastrichtian)

Hell Creek Formation

Flag of the United States.svg  United States
(Flag of South Dakota.svg  South Dakota)

A caenagnathid theropod. The type species is E. infernalis.

Eoneophron infernalis.png
Fona [41] Gen. et sp. novAvrahami et al.Late Cretaceous (Cenomanian) Cedar Mountain Formation Flag of the United States.svg  United States
(Flag of Utah.svg  Utah)
A thescelosaurid ornithischian. The type species is F. herzogae. Fona herzogae.png

Gandititan [42]

Gen. et sp. nov

Valid

Han et al.

Late Cretaceous (Cenomanian-Turonian)

Zhoutian Formation

Flag of the People's Republic of China.svg  China

A titanosaur sauropod. The type species is G. cavocaudatus.

Gandititan UDL.png

Harenadraco [43]

Gen. et sp. nov

Lee et al.

Late Cretaceous

Barun Goyot Formation

Flag of Mongolia.svg  Mongolia

A troodontid theropod. The type species is H. prima.

Harenadraco prima.png

Hesperonyx [44]

Gen. et sp. nov

Valid

Rotatori et al.

Late Jurassic

Lourinhã Formation

Flag of Portugal.svg  Portugal

An early diverging iguanodontian ornithopod, possibly a dryomorphan. The type species is H. martinhotomasorum.

Hesperonyx UDL.png

Inawentu [45]

Gen. et sp. nov

Valid

Filippi et al.

Late Cretaceous (Santonian)

Bajo de la Carpa Formation

Flag of Argentina.svg  Argentina

A titanosaur sauropod. The type species is I. oslatus. Announced in 2023; the final article version was published in 2024.

Inawentu oslatus.png

Jingiella [46]

Gen. et sp. nov

Ren et al.

Late Jurassic

Dongxing Formation

Flag of the People's Republic of China.svg  China

A mamenchisaurid sauropod. The type species is J. dongxingensis. The initially proposed name is preoccupied by Jingia Chen, 1983. [47] The replacement name was published in an addendum. [48]

Jingiella UDL.png

Kiyacursor [49]

Gen. et sp. nov

Averianov et al.

Early Cretaceous (Aptian)

Ilek Formation

Flag of Russia.svg  Russia
(Flag of Kemerovo Oblast.svg  Kemerovo Oblast)

A noasaurid theropod. The type species is K. longipes.

Kiyacursor PM (white bg).png

Koleken [50]

Gen. et sp. nov

Pol et al.

Late Cretaceous (Campanian-Maastrichtian)

La Colonia Formation

Flag of Argentina.svg  Argentina

An abelisaurid theropod. The type species is K. inakayali.

Lokiceratops [51]

Gen. et sp. nov

Valid

Loewen et al.

Late Cretaceous (Campanian)

Judith River Formation

Flag of the United States.svg  United States
(Flag of Montana.svg  Montana)

An centrosaurine ceratopsian. The type species is L. rangiformis.

Lokiceratops rangiformis.png

Minqaria [52]

Gen. et sp. nov

Longrich et al.

Late Cretaceous (Maastrichtian)

Ouled Abdoun Basin

Flag of Morocco.svg  Morocco

A lambeosaurine hadrosaurid belonging to the tribe Arenysaurini. The type species is M. bata.

Minqaria.png
Musankwa [53] Gen. et sp. novBarrett et al. Late Triassic (Norian) Pebbly Arkose Formation Flag of Zimbabwe.svg  Zimbabwe A massopodan sauropodomorph. The type species is M. sanyatiensis. Musankwa Skeletal.svg

Riojavenatrix [54]

Gen. et sp. nov

Isasmendi et al.

Early Cretaceous (Barremian-Aptian)

Enciso Group

Flag of Spain.svg  Spain

A spinosaurid theropod. The type species is R. lacustris.

Riojavenatrix UDL.png

Sidersaura [55]

Gen. et sp. nov

Valid

Lerzo et al.

Late Cretaceous (Cenomanian-Turonian)

Huincul Formation

Flag of Argentina.svg  Argentina

A rebbachisaurid sauropod. The type species is S. marae.

Sidersaura UDL.png

Thyreosaurus [56]

Gen. et sp. nov

Zafaty et al.

Middle Jurassic

El Mers Group

Flag of Morocco.svg  Morocco

A stegosaurian. The type species is T. atlasicus.

Thyreosaurus Skeletal.svg

Tiamat [57]

Gen. et sp. nov

Pereira et al.

Cretaceous (Albian–Cenomanian)

Açu Formation

Flag of Brazil.svg  Brazil

A basal titanosaur sauropod. The type species is T. valdecii.

Tiamat Skeletal.svg
Tietasaura [58] Gen. et sp. novBandeira et al.Early Cretaceous (ValanginianHauterivian) Marfim Formation Flag of Brazil.svg  Brazil An elasmarian ornithopod. The type species is T. derbyiana. Tietasaura Skeletal.svg

Titanomachya [59]

Gen. et sp. nov

Pérez-Moreno et al.

Late Cretaceous (Campanian-Maastrichtian)

La Colonia Formation

Flag of Argentina.svg  Argentina

A titanosaur sauropod. The type species is T. gimenezi.

Tyrannosaurus mcraeensis [60]

Sp. nov

Valid

Dalman et al.

Late Cretaceous (Campanian-Maastrichtian)

Hall Lake Formation

Flag of the United States.svg  United States
(Flag of New Mexico.svg  New Mexico)

A tyrannosaurine; a species of Tyrannosaurus .

Tyrannosaurus mcraeensis (skull reconstruction).png

Udelartitan [61]

Gen. et sp. nov

In press

Soto et al.

Late Cretaceous

Guichón Formation

Flag of Uruguay.svg  Uruguay

A titanosaur sauropod belonging to the group Saltasauroidea. The type species is U. celeste.

Udelartitan UDL.png

Urbacodon norelli [62]

Sp. nov

Wang et al.

Late Cretaceous

Iren Dabasu Formation

Flag of the People's Republic of China.svg  China

A troodontid theropod; a species of Urbacodon .

Vectidromeus [63]

Gen. et sp. nov

Valid

Longrich et al.

Early Cretaceous (Barremian)

Wessex Formation

Flag of the United Kingdom.svg  United Kingdom

A hypsilophodontid. The type species is V. insularis. Announced in 2023; the final article version was published in 2024.

Vectidromeus UDL.png

Yanbeilong [64]

Gen. et sp. nov

Valid

Jia et al.

Early Cretaceous (Albian)

Zuoyun Formation

Flag of the People's Republic of China.svg  China

A stegosaurian. The type species is Y. ultimus.

Yanbeilong ultimus.png

General non-avian dinosaur research

Saurischian research

Theropod research

  • A study on the femoral shape variation in theropods, providing evidence of evolution of similar adaptations to gigantism in large-bodied theropods regardless of their phylogenetic affinities, is published by Pintore et al. (2024). [81]
  • Dridi et al. (2024) describe tracks of medium to large-sized theropods from the Lower Cretaceous (HauterivianBarremian) strata from the Jebel Kebar locality (Bouhedma Formation, Tunisia), extending known geographic range of non-avian theropods to higher latitudes within Gondwana. [82]
  • A study on the affinities of shed tooth crowns of theropods from the Turonian-Coniacian Portezuelo Formation (Argentina), providing evidence of a previously undocumented diversity of theropods from this formation, is published by Meso et al. (2024). [83]
  • Isasmendi et al. (2024) describe new and revise known theropod teeth from the Maastrichtian strata from the South Pyrenean Basin (Spain), expanding known diversity of theropods from this basin and reporting evidence of theropod turnover during the Maastrichtian. [84]
  • McLarty & Esperante (2024) describe theropod tracks from the Maastrichtian strata from the Carreras Pampa tracksite (Bolivia) interpreted as likely preserving evidence of the trackmakers pausing during movement, bypassing an obstacle and crouching. [85]
  • Mohabey et al. (2024) review and redescribe Laevisuchus indicus , Jubbulpuria tenuis and Compsosuchus solus , and describe a new noasaurid dentary from central India with procumbent dentition similar to the one present in Masiakasaurus . [86]
  • A study on the affinities of isolated theropod teeth from the Kem Kem Group (Morocco) is published by Hendrickx et al. (2024), who identify teeth of abelisaurids, spinosaurines, carcharodontosaurids and a non-abelisauroid ceratosaur or a megaraptoran. [87]
  • A probable ceratosaurid dentary is described from the Toarcian Cañadón Asfalto Formation (Argentina) by Pradelli, Pol & Ezcurra (2024), expanding known theropod diversity from this formation. [88]
  • A study on the affinities of isolated theropod teeth from the Bauru Basin (Brazil) is published by Delcourt et al. (2024), who argue that the geographical distribution of abelisaurids in South America was influenced by climatic conditions. [89]
  • Ribeiro et al. (2024) identify a theropod tooth from the Upper Jurassic-Lower Cretaceous Missão Velha Formation (Brazil) as the oldest abelisaurid record in the South America reported to date. [90]
  • A study in the bone histology of a mid-sized abelisaurid from the Upper Cretaceous Serra da Galga Formation (Brazil) is published by Aureliano et al. (2024), who report that, despite living in a semiarid tropical environment, the studied specimen had a growth rate similar to those of the Patagonian abelisaurids. [91]
  • A study on the skeletal pathologies affecting known specimens of brachyrostran abelisaurids is published by Baiano et al. (2024), who diagnose the fusion of two caudal vertebrae of the holotype specimen of Aucasaurus garridoi as congenital malformation and diagnose partial fusion of five caudal vertebrae of the holotype of Elemgasem nubilus as spondyloraptropathy, in both cases representing the first occurrences of the diagnosed pathologies among non-tetanuran theropods. [92]
  • Cerroni, Otero & Novas (2024) present the reconstruction of the pelvic and hindlimb musculature of Skorpiovenator bustingorryi . [93]
  • Cau (2024) reinterprets "compsognathid" theropod specimens as juveniles of members of non-maniraptoriform tetanuran groups. [94]
  • Montealegre, Castillo-Visa & Sellés (2024) describe previously unpublished fossil material of theropods (cf. Protathlitis and a carcharodontosaurid which might be distinct from Concavenator ) from the Barremian Arcillas de Morella Formation (Spain). [95]
  • Yun (2024) identifies convergent similarities in craniodental anatomy between spinosaurs and phytosaurs. [96]
  • Myhrvold et al. (2024) use statistical analyses to reconsider previous descriptions by Fabbri et al. (2022) of spinosaurs such as Spinosaurus as subaqueous foragers, [97] and provide evidence that Spinosaurus was likely not an aquatic pursuit predator. [98]
  • Evidence from the study of patterns in skull shape, interpreted as indicating that Spinosaurus fed on aquatic prey and likely used the "stand-and-wait" predation strategy, is presented by Smart & Sakamoto (2024). [99]
  • Buffetaut & Tong (2024) reinterpret a purported ichthyosaur tooth from the Sao Khua Formation collected in 1962 and described in 1963 as a spinosaurid tooth and the first finding of a non-avian dinosaur fossil reported from Thailand. [100]
  • A study on tooth replacement pattern of Guanlong wucaii is published by Ke, Pei & Xu (2024). [101]
  • Teeth of a probable basal tyrannosauroid are described from the Upper Jurassic Phu Kradung Formation (Thailand) by Chowchuvech et al. (2024). [102]
  • Xing et al. (2024) describe large tyrannosauroid teeth from the Maastrichtian Dalangshan Formation, representing the southernmost record of tyrannosauroids in China reported to date. [103]
  • Słowiak, Brusatte & Szczygielski (2024) reevaluate the fossil material attributed to Bagaraatan ostromi , interpreting the holotype as an indeterminate juvenile tyrannosaurid, and reporting that some of the fossils originally attributed to B. ostromi are actually caenagnathid bones. [104]
  • Yun (2024) estimates mandibular force profiles of Alioramus altai and Qianzhousaurus sinensis , interpreting the mandibles of the studied theropods as likely unsuited for delivering powerful bites and enduring high stresses caused by capturing, holding and dismembering large prey. [105]
  • A study on the affinities of tyrannosaurines is published by Warshaw, Barrera Guevara & Fowler (2024), who contest the conclusions of the study of Scherer & Voiculescu-Holvad (2023), [106] recovering recognized Daspletosaurus species as representing a single anagenetic lineage ancestral to Tyrannosaurus-line tyrannosaurines. [107]
  • Longrich & Saitta (2024) review the taxonomic status of Nanotyrannus and argue that multiple lines of evidence support it as a distinct, small-bodied, possibly non-tyrannosaurid taxon, rather than an immature form of Tyrannosaurus . [108]
  • A study on the phylogenetic relationships of Kinnareemimus khonkaenensis is published by Samathi (2024). [109]
  • Description of the skeletal anatomy of Nothronychus graffami and N. mckinleyi, providing evidence of the presence of traits convergent with extant birds, ornithischian dinosaurs and titanosaur sauropods, is published by Smith & Gillette (2024). [110]
  • Park et al. (2024) propose that early pennaraptorans might have used their pennaceous feathers to flush hiding insects and to generate lift or drag during the pursuit of the flushed insects, and propose that such use of the pennaceous feathers might have contributed to the evolution of larger and stiffer feathers. [111]
  • A characterization of how number and shape of flight feathers correlate with locomotory style in extant birds is published by Kiat & O'Connor (2024). Extrapolating these patterns to Mesozoic pennaraptorans, the authors suggest that Caudipteryx and anchiornithines may have been secondarily flightless. [112]
  • A study on the evolution of the pectoral girdle of pennaraptorans is published by Wu et al. (2024), who report evidence of modifications changing the range of motion of the forelimb that preceded the origin of flight in paravians, as well as evidence of subsequent flight adaptive modifications in avialans. [113]
  • Meade et al. (2024) report evidence indicating that the ability of the skull to resist large mechanical stresses appeared early in oviraptorosaur evolution, before the appearance of the highly modified oviraptorid cranial architecture. [114]
  • The first caenagnathid fossil material from the upper Campanian De-na-zin Member of the Kirtland Formation (New Mexico, United States) is described by Funston, Williamson & Brusatte (2024). [115]
  • Qiu et al. (2024) describe the skeletal anatomy of the wrist of Heyuannia huangi , providing evidence of a specialized wrist morphology that was functionally convergent with the wrist morphology of extant birds. [116]
  • Description of the skeletal anatomy of Oksoko avarsan is published by Funston (2024). [117]
  • Zhu, Wang & Wang (2024) study the microstructural variation of elongatoolithid eggs from China, and interpret the studied variation as indicating that not all elongatoolithid eggshells can be related to oviraptorosaurs. [118]
  • A study on the skull shape and bite mechanics of dromaeosaurids is published by Tse, Miller & Pittman (2024), who interpret Deinonychus antirrhopus as adapted to taking large vertebrate prey, and interpret Halszkaraptor escuilliei as unlikely to feed on fish, and more likely to have a feeding ecology similar to those of extant waterfowl. [119]
  • Possible dromaeosaurid eggs are described from the Upper Cretaceous Lianhe Formation (China) by Wu et al. (2024), who name a new ootaxon Gannanoolithus yingliangi , and interpret the discovery of paired eggs of Gannanoolithus as possible evidence that dromaeosaurids had paired functional oviducts. [120]
  • Gianechini, Colli & Makovicky (2024) present a reconstruction of the pelvic and hindlimb musculature of Buitreraptor gonzalezorum . [121]
  • Based on comparisons to extant birds, joint poses in the foot of Deinonychus during its walk cycle are reconstructed by Manafzadeh, Gatesy & Bhullar (2024). [122]
  • Description of the braincase and cranial endocast of Sinovenator changii , interpreted as morphologically intermediate between basal theropods and extant birds, is published by Yu et al. (2024). [123]
  • Xing et al. (2024) describe tracks from the Upper Cretaceous Shaxian Formation (Fujian, China) which might have been produced by a large-bodied (estimated hip height of over 1.8 m) troodontid, and name a new ichnotaxon Fujianipus yingliangi . [124]

Sauropodomorph research

  • Silva et al. (2024) describe fossil material of a member or a relative of the group Bagualosauria from the Vila Botucaraí site (Candelária Sequence of the Santa Maria Supersequence, Brazil), representing the first sauropodomorph reported from this site. [125]
  • Evidence of variability of the pneumacity patterns of the cervical and dorsal vertebra in Plateosaurus is presented by Regalado Fernández (2024). [126]
  • Redescription of the holotype and a study on the affinities of Plateosaurus trossingensis is published by Schaeffer (2024). [127]
  • Zhao et al (2024) describe a new juvenile–subadult massospondylid specimen from the Lower Jurassic Lufeng Formation (Yunnan, China), increasing known diversity of massospondylids from Asia. [128]
  • "Gyposaurus" sinensis is interpreted as a probable junior synonym of Lufengosaurus huenei by Wang, Zhao & You (2024). [129]
  • Barrett & Choiniere (2024) redescribe the skeletal anatomy of Melanorosaurus readi and designate the lectotype of this species. [130]
  • Using Spinophorosaurus as an example, Vidal (2024) explains how virtual 3D models of sauropods have enabled an understanding of their biomechanics. [131]
  • Agustí, Alcalá & Santos-Cubedo (2024) propose that sauropod gigantism was an adaptation that increased the ability of sauropods to travel great distances, necessitated by pronounced seasonal changes. [132]
  • Butler et al. (2024) describe an assemblage of tracks produced by large-bodied sauropods passing through coastal lagoonal environment from the earliest Cretaceous strata of the Durlston Formation (Dorset, United Kingdom), representing the largest dinosaur track site accessible within the Purbeck Group reported to date. [133]
  • Boisvert et al. (2024) describe a new specimen of Haplocanthosaurus sp. from the Dry Mesa Dinosaur Quarry (Colorado, United States), extending known range of the genus into the true Brushy Basin Member of the Morrison Formation, and likely representing the geologically youngest occurrence of Haplocanthosaurus on the Colorado Plateau. [134]
  • King et al. (2024) report evidence of a previously unknown form of pneumaticity in a rib of a member of the genus Apatosaurus , and propose that rib pneumaticity among apatosaurines is individually variable. [135]
  • Windholz et al. (2024) describe a new rebbachisaurid caudal vertebra from the Cenomanian Candeleros Formation (Argentina), providing new information on the caudal anatomy and pneumaticity in rebbachisaurids. [136]
  • Gomez et al. (2024) describe new titanosauriform fossils from the Portezuelo Formation (Argentina), expanding known diversity of sauropods from this formation. [137]
  • Beeston et al. (2024) describe new sauropod material from the Winton Formation (Australia), and interpret Australotitan cooperensis as an indeterminate diamantinasaurian that is likely a junior synonym of Diamantinasaurus matildae . [138]
  • Filippi et al. (2024) study fossil material of sauropods from the Cerro Overo – La Invernada area (Bajo de la Carpa Formation; Neuquén Province, Argentina), interpreted as suggestive of the presence of a diverse fauna of titanosauriforms coexisting in the environment during the Santonian. [139]
  • A study on the taphonomy of the fossil material of Kaijutitan maui and on its bone histology is published by Filippi, Previtera & Garrido (2024). [140]
  • Vidal et al. (2024) study the range of motion of the axial series of Trigonosaurus pricei , and interpret it as capable of high elevation of the neck. [141]
  • A description and study of the morphological variability of sauropod appendicular remains from Maastrichtian sites of the Hațeg, Transylvanian, and Rusca Montană basins (Romania) is published by Mocho, Pérez-García & Codrea (2024), who interpret the studied remains as indicative of the presence of four or five sauropod taxa on the Hațeg Island during the Maastrichtian, including a titanosaur lineage with an extremely elongated manus. [142]
  • An overview of the largest known sauropods from Argentina is published by Calvo (2024). [143]

Ornithischian research

Thyreophoran research

Cerapod research

  • A review of Early Cretaceous Spanish styracosterns from the Maestrat Basin published by Santos-Cubedo (2024). [156]
  • Escanero-Aguilar et al. (2024) describe skull material of a hadrosauriform ornithopod from the Lower Cretaceous Castrillo de la Reina Formation (Spain), interpreted as more derived than Iguanodon but more basal than Proa , and expanding known diversity of ornithopods from the Cameros Basin. [157]
  • Nikolov, Dochev, & Brusatte (2024) test the ontogenetic age of small hadrosauroid bones from the Late Cretaceous (Maastrichtian) Kaylaka Formation (Bulgaria), and determine that the specimen likely belonged to a late juvenile or young subadult, rather than a dwarved adult, and suggest that large terrestrial animals were able to populate some European islands via a cyclically appearing or short-lived dispersal route. [158]
  • The first described hadrosaurid footprints from the Horseshoe Canyon Formation are described by Powers et al. (2024), who assign them to the ichnospecies Hadrosauropodus langstoni. [159]
  • Evidence from the study of a skull of a juvenile hadrosaurine from the Campanian Dinosaur Park Formation (Alberta, Canada), interpreted as indicative of differences in the dental battery development between hadrosaurid species which might have been related to dietary differences during early ontogeny, is presented by Warnock-Juteau et al. (2024). [160]
  • Sharpe et al. (2024) describe fossil material of a probable immature specimen of Edmontosaurus regalis from the Horseshoe Canyon Formation, and interpret its similarities to Ugrunaaluk kuukpikensis as supporting the referral of the Alaskan saurolophine material to Edmontosaurus cf. regalis. [161]
  • Description of the morphology of the skull and endocranium of Psittacosaurus sibiricus , based on the study of both juvenile and adult specimens, is published by Podlesnov et al. (2024). [162]
  • A description endocranial anatomy of the Psittacosaurus lujiatunensis published by Sakagami et al. (2024). [163]
  • Yang et al. (2024) describe a well-preserved scaled skin of a specimen of Psittacosaurus from the Early Cretaceous Jehol Biota of China, providing evidence of preservation of epidermal layers, corneocytes and melanosomes, and interpret the studied specimen as indicative of co-occurrence of feathers and reptile-type skin in non-feathered regions of the skin in Psittacosaurus. [164]
  • Witton & Hing (2024) argue that there is no compelling evidence indicating that the development of the idea of the griffin was inspired by the discovery of fossils of Protoceratops . [165]
  • Barrera Guevara et al. (2024) reinterpret fossil material of Coahuilaceratops magnacuerna as derived from Cerro Huerta Formation (and representing the first dinosaur taxon described from this formation) rather than from Cerro del Pueblo Formation. [166]

Birds

New bird taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages

Ardenna buchananbrowni [167]

Sp. nov

Valid

Tennyson et al.

Pliocene (Waipipian)

Tangahoe Formation

Flag of New Zealand.svg  New Zealand

A species of Ardenna .

Chloephaga dabbenei [168]

Sp. nov

Valid

Agnolín, Álvarez Herrera & Tomassini

Pleistocene

Flag of Argentina.svg  Argentina

A species of Chloephaga .

Enkuria [169]

Gen. et sp. et comb. nov

Valid

Zelenkov

Pliocene and Pleistocene

Crimea

A relative of the grey partridge. The type species is E. voinstvenskyi; genus also includes "Phasianus" etuliensis Bocheński & Kurochkin (1987) from Moldova.

Eocypselus geminus [170] Sp. novIn pressMayr & Kitchener Eocene London Clay Flag of the United Kingdom.svg  United Kingdom A species of Eocypselus.
Eocypselus grandissimus [170] Sp. novIn pressMayr & Kitchener Eocene London Clay Flag of the United Kingdom.svg  United Kingdom A species of Eocypselus.
Eocypselus paulomajor [170] Sp. novIn pressMayr & Kitchener Eocene London Clay Flag of the United Kingdom.svg  United Kingdom A species of Eocypselus.
Fluvioviridavis michaeldanielsi [171] Sp. novMayr & Kitchener Eocene London Clay Flag of the United Kingdom.svg  United Kingdom A species of Fluvioviridavis.
Fluvioviridavis nazensis [171] Sp. novMayr & Kitchener Eocene London Clay Flag of the United Kingdom.svg  United Kingdom A species of Fluvioviridavis.

Imparavis [172]

Gen. et sp. nov

In press

Wang et al.

Early Cretaceous

Jiufotang Formation

Flag of the People's Republic of China.svg  China

An enantiornithine. The type species is I. attenboroughi.

Nasiornis [173] Gen. et sp. novIn pressMayr & Kitchener Eocene London Clay Flag of the United Kingdom.svg  United Kingdom A messelornithid. The type species is N. messelornithoides.

Paralyra [174]

Gen. et comb. nov

Valid

Zelenkov

Pliocene and Pleistocene

Flag of Poland.svg  Poland

A grouse; a new genus for "Lagopus lagopus" atavus Jánossy (1974), originally described from the Rębielice Królewskie 1 locality in Poland, subsequently also described from the Taurida Cave in Crimea. [174]

? Parvirallus incertus [173] Sp. novIn pressMayr & KitchenerEoceneLondon ClayFlag of the United Kingdom.svg  United Kingdom A messelornithid; a possible species of Parvirallus.
Phalacrocorax bakonyiensis [175] Sp. novValidHorváth, Futó, & Kessler Miocene Flag of Hungary.svg  Hungary A cormorant; a species of Phalacrocorax .

Pristineanis [176]

Gen. et 2 sp. et comb. nov

Valid

Mayr & Kitchener

Eocene

London Clay

Flag of the United Kingdom.svg  United Kingdom
Flag of the United States.svg  United States

A possible member of Piciformes. The type species is P. minor; genus also includes new species P. major, as well as "Neanis" kistneri Feduccia (1973).

Septencoracias simillimus [176]

Sp. nov

Valid

Mayr & Kitchener

Eocene (Ypresian)

London Clay

Flag of the United Kingdom.svg  United Kingdom

A stem group roller belonging or related to the family Primobucconidae.

Walbeckornis waltonensis [173] Sp. novIn pressMayr & KitchenerEoceneLondon ClayFlag of the United Kingdom.svg  United Kingdom A species of Walbeckornis .

Waltonirrisor [176]

Gen. et sp. nov

Valid

Mayr & Kitchener

Eocene (Ypresian)

London Clay

Flag of the United Kingdom.svg  United Kingdom

A member of Upupiformes. The type species is W. tendringensis.

Wunketru [177]

Gen. et comb. nov

In press

De Mendoza, Degrange & Tambussi

Eocene

Las Flores Formation

Flag of Argentina.svg  Argentina

A member of Anseriformes of uncertain affinites; a new genus for "Telmabates" howardae.

Avian research

Pterosaurs

New pterosaur taxa

NameNoveltyStatusAuthorsAgeType localityCountryNotesImages
Ceoptera [217] Gen. et sp. novValidMartin-Silverstone et al. Middle Jurassic Kilmaluag Formation Flag of the United Kingdom.svg  United Kingdom A darwinopteran. The type species is C. evansae.

Haliskia [218]

Gen. et sp. nov

Valid

Pentland et al.

Early Cretaceous (Albian)

Toolebuc Formation

Flag of Australia (converted).svg  Australia

A member of Anhangueria. The type species is H. peterseni.

Haliskia Life Restoration.png
Torukjara [219] Gen. et sp. novValidPêgas Early Cretaceous Caiuá Group Flag of Brazil.svg  Brazil A tapejarid. The type species is T. bandeirae. Torukjara CP.V 8175.png

Pterosaur research

Other archosaurs

Other archosaur research

General research

Related Research Articles

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This article records new taxa of fossil archosaurs of every kind that are scheduled described during the year 2022, as well as other significant discoveries and events related to paleontology of archosaurs that are scheduled to occur in the year 2022.

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