2023 in archosaur paleontology
| |||
---|---|---|---|
+... |
This article records new taxa of every kind of fossil archosaur that were scheduled to be described during 2023, as well as other significant discoveries and events related to the paleontology of archosaurs that were published in 2023.
Pseudosuchians
[edit]New pseudosuchian taxa
[edit]Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
Valid |
Darlim et al. |
Middle Pleistocene to Holocene |
An altirostral species of alligator closely related to the Chinese alligator. |
||||
Gen. et sp. nov |
Martin et al. |
Miocene |
An early diverging crocodile. The type species is A. chiangmuanensis. |
|||||
Sp. nov |
Martins et al. |
Late Cretaceous |
A baurusuchid. |
|||||
Baru iylwenpeny[4] | Sp. nov | Yates, Ristevski, & Salisbury | Late Miocene | Alcoota Fossil Beds | Australia | A member of the clade Mekosuchinae. | ||
Sp. nov |
Valid |
|||||||
Gen. et comb. nov |
Martin et al. |
Eocene (Bartonian) |
A member of the family Sebecidae; a new genus for "Atacisaurus" crassiproratus Astre (1931). |
|||||
Huenesuchus[7] |
Gen. nov. |
Disputed |
Kischlat |
A replacement name for Prestosuchus Huene 1938, considered to be a nomen nudum. |
||||
Kryphioparma[8] | Gen. et sp. nov | Reyes, Parker, & Heckert | Late Triassic (Norian) | Chinle Formation | United States ( Arizona) |
An aetosaur. The type species is K. caerula. | ||
Gen. et sp. nov |
Valid |
Sennikov |
Early Triassic |
A member of the family Rauisuchidae. The type species is S. basileus. Published online in 2023, but the issue date is listed as December 2022.[9] |
||||
Sp. nov |
Valid |
Girard et al. |
Late Jurassic |
|||||
Gen. et sp. nov |
Wilberg et al. |
Early Jurassic (Pliensbachian) |
An early diverging thalattosuchian. |
|||||
Gen. et sp. nov |
Valid |
Haldar, Ray & Bandyopadhyay |
A typothoracine aetosaur. The type species is V. armatum. |
General pseudosuchian research
[edit]- Evidence of the impact of the interplay of abiotic and biotic processes on the evolution of pseudosuchians is presented by Payne et al. (2023).[13]
- A study on the biomechanical properties of the skull of Riojasuchus tenuisceps is published by Taborda, Von Baczko & Desojo (2023), who propose that R. tenuisceps could have had a wading habit, feeding on small-sizey prey caught from the shoreline.[14]
- A study on the bone histology of Decuriasuchus quartacolonia is published by Farias et al. (2023), who interpret their findings as indicative of early ontogenetic stage of known specimens, which might have stayed in group to obtain food and avoid predation before reaching maturity, as well as opening the possibility that D. quartacolonia may represent an earlier growth stage of the larger Prestosuchus chiniquensis.[15]
- A study on the bone histology of Fasolasuchus tenax and Prestosuchus chiniquensis, providing evidence of slower growth rate in the latter taxon, is published by Ponce et al. (2023).[16]
- A study on the biomechanics of the skull of Saurosuchus galilei is published by Fawcett et al. (2023), who interpret Saurosuchus as having a weak bite for an animal of its size, possessing several mechanically weak features in the skull, and likely avoiding tooth–bone interactions while feeding.[17]
- Redescription of the braincase of Saurosuchus galilei and a study of its sensorial capacities is published by von Baczko et al. (2023), who report evidence interpreted as indicative of an enhanced olfactory acuity.[18]
- An osteoderm and tooth of a 'rauisuchian', likely a rauisuchid, are described from the lower Elliot Formation of South Africa, and identify two potential morphotypes of rauisuchid in the lower Elliot.[19]
- Redescription of the anatomy of the skull of Shuvosaurus inexpectatus is published by Lehane (2023).[20]
Aetosaur research
[edit]- A study on the humeral histology in specimens of Aetosaurus ferratus from the Kaltental site (Lower Stubensandstein, Germany) is published by Teschner et al. (2023), who interpret the studied specimens as juveniles, and interpret the accumulation of small-sized specimens at Kaltental as possible evidence of gregarious behavior in juveniles of A. ferratus.[21]
- Parker, Reyes & Marsh (2023) describe a new specimen of Typothorax coccinarum from Petrified Forest National Park (Arizona, United States) that is the largest aetosaur specimen reported to date, and report that the studied individual likely had not yet reached skeletal maturity, indicating that body size may not be a reliable indicator of maturity in aetosaurs.[22]
Crocodylomorph research
[edit]- A study on the bone histology of early crocodylomorphs is published by Botha et al. (2023), who interpret their findings as indicating that the transition from high growth rates of earlier-diverging pseudosuchians to slower rates of bone deposition during mid-late ontogeny happened around the origin of Crocodylomorpha during the Late Triassic.[23]
- Revision of the fossil material of Saltoposuchus connectens is published by Spiekman (2023), who considers S. connectens to be a taxon distinct from Terrestrisuchus gracilis, and interprets the histology of the femur of the second-largest studied specimen as indicative of sustained high growth rates.[24]
- Redescription of Terrestrisuchus gracilis is published by Spiekman et al. (2023), who report evidence indicative of extensive pneumatization of the posterior skull region, as well as probable anatomical adaptations to non-nocturnal, possibly cathemeral activity patterns.[25]
- Evidence from the osteological correlates of the trigeminal nerve in extant and fossil taxa, interpreted as indicative of an increase in sensory abilities in Early Jurassic crocodylomorphs, preceding their transitions to a semiaquatic habitat, is presented by Lessner et al. (2023).[26]
- A study on the relationship between osteoderm relative area of pits and terrestrial or aquatic lifestyle in extant and extinct crocodyliforms, indicating that taxa with lower the degree of ornamentation were more likely to be terrestrial, is published by de Araújo Sena & Cubo (2023).[27]
- A study on palatal grooves of thalattosuchians is published by Young et al. (2023), who report that the studied grooves were continuous with ossified canals that connected the oral cavity to the nasal cavity, and interpret the studied grooves and canals as likely evidence of the existence of a heat exchange pathway linking the palatal vascular plexus to the vessels that supplied blood to the brain and eyes.[28]
- A study on the growth patterns of Macrospondylus bollensis is published by Johnson, Amson & Maxwell (2023).[29]
- Young et al. (2023) describe thalattosuchian fossil material from deposits in European Russia ranging from Bajocian to Berriasian or Valanginian in age, including fossil material of cf. Thalattosuchus, Torvoneustes and Tyrannoneustes which expands known geographical range of these taxa, as well as including the oldest record of Geosaurini reported to date.[30]
- Revision of the fossil record of thalattosuchians from the Jurassic Rosso Ammonitico Veronese (Italy), as well as description of three new metriorhynchoid specimens (including a specimen from the upper Bajocian-upper Bathonian of Cima del Porco representing one of the oldest known metriorhynchids, and a Bajocian specimen which might have beaan a metriorhynchid or a closely related metriorhynchoid), is published by Serafini et al. (2023).[31]
- Evidence indicative of limited evolutionary convergence in the morphology of the postcranial skeletons of members of Thalattosuchia and Dyrosauridea, even when found within similar environments, is presented by Scavezzoni & Fischer (2023).[32]
- New specimen of Hsisosuchus of uncertain specific assignment, providing new information on the shape and arrangement of the osteoderms in the ventral trunk shield of members of this genus, is described from the Upper Jurassic of Yunnan (China) by Wu et al. (2023).[33]
- A study on the notosuchian physiology is published by de Araújo Sena et al. (2023), who find maximal rates of oxygen consumption of notosuchians to be lower than those of extant mammals and monitor lizards but higher than those of extant crocodilians during periods of intensive activity, and interpret notosuchians as likely having a more active lifestyle than extant crocodilians.[34]
- A study on possible effects of climate, body size and diet on the survival of terrestrial notosuchians during the Cretaceous–Paleogene extinction event is published by Aubier et al. (2023), who find evidence of increase in body size during the Late Cretaceous which may be related to the shift from omnivorous to carnivorous diet, but find the studied data insufficient to list definitive reasons for the survival of sebecids into the Cenozoic.[35]
- A study on the bone histology of a femur of Araripesuchus wegeneri is published by Faure-Brac & Cubo (2023), who find no evidence for the presence of sustained fibrolamellar complex in the studied taxon, and interpret this finding as consistent with the ectothermic regime inferred for notosuchians, but not with their high maximum metabolic rates and with upright stance of A. wegeneri, which therefore had a phenotype with no equivalent in the extant fauna.[36]
- A study on the long bone microstructure in Notosuchus terrestris, providing evidence of high growth rates interrupted by periods of decreased or arrested growth, is published by Navarro, Cerda & Pol (2023).[37]
- A study on the bone histology of Stratiotosuchus maxhechti, interpreted as indicative of growth dynamics similar to those of medium-to-large theropods, is published by Andrade et al. (2023), who argue that niche partitioning between baurusuchids and theropods was more likely than competitive exclusion.[38]
- Description of new fossil material of itasuchid crocodyliforms from the Upper Cretaceous Bauru Group (Brazil) is published by Pinheiro et al. (2023), who also confirm the monophyly of Itasuchidae with some variation in its content, and find the South American itasuchid species to occupy a crocodyliform morphospace, possibly indicating distinct niche occupations.[39]
- A new mandibular ramus referred to Hamadasuchus cf. reboulli is described by Pochat-Cottilloux et al., who propose an emended diagnosis of the taxon and argue that only three specimens are actually referrable to this species. They further discuss multiple anatomical characters of the mandible that they suggest represent intraspecific or ontogenetic differences and are not diagnostically valuable. As a consequence, it is suggested that Antaeusuchus may be a species of Hamadasuchus.[40]
- Pochat-Cottilloux et al. (2023) describe the endocranial structures of Hamadasuchus, providing evidence of adaptations to terrestrial lifestyle.[41]
- A study on the ecology of sebecids from the Paleocene locality of Tiupampa (Bolivia), using a multi-isotopic proxy approach, is published by Pochat-Cottilloux et al. (2023), who interpret their findings as indicative of ectothermic thermoregulation and terrestrial lifestyle in the studied crocodylomorphs.[42]
- A study on the biogeography of neosuchians throughout their evolutionary history, providing evidence of the impact of saltwater tolerance of neosuchians from different subclades on their historical biogeography, is published by Groh et al. (2023).[43]
- Description of a new specimen of Acynodon adriaticus from the Campanian Villaggio del Pescatore site (Italy) and a study on the affinities of this species is published by Muscioni et al. (2023).[44]
- Revision of the fossil material of Cenomanian crocodyliforms from the Arlington Archosaur Site (Woodbine Group; Texas, United States), providing evidence of the presence of at least five taxa with different snout shapes and body size which might be related to niche partitioning, is published by Adams, Drumheller & Noto (2023).[45]
- A study on the taxonomic diversity, phylogenetic relationships and evolutionary history of Australasian crocodyliforms is published by Ristevski et al. (2023).[46]
- Venczel (2023) describes new fossil material of Diplocynodon kochi from the Eocene Transylvanian Basin (Romania), extending known fossil record of this species to four new localities.[47]
- A tooth of a member of the genus Purussaurus is described from the Toma Vieja locality near Paraná City (traditionally considered as the base of Ituzaingó Formation) by Bona et al. (2023), representing the first record of this genus from the Late Miocene of Argentina and the southernmost occurrence of a member of this genus reported to date.[48]
- Taxonomic revision of the genus Mourasuchus is published by Cidade & Hsiou (2023).[49]
- A study on the neuroanatomy and phylogenetic affinities of Portugalosuchus azenhae is published by Puértolas-Pascual et al. (2023), who recover Portugalosuchus as a member of Gavialoidea most closely related to Thoracosaurus neocesariensis.[50]
- A collection of isolated gavialoid teeth is reported from the shallow marine deposits of Eocene Turnu Roșu (Romania) by Venczel et al. (2023), who recognize a minimum of five morphotypes.[51]
- Burke & Mannion (2023) present a reconstruction of the neuroanatomy and neurosensory apparatus of "Tomistoma" dowsoni, providing evidence that this gavialoid displayed an intermediate morphology between those of extant gharials and false gharials.[52]
- Redescription of "Tomistoma" taiwanicus is published by Cho & Tsai (2023), who transfer this species to the genus Toyotamaphimeia.[53]
- A study on the inner braincase anatomy of Voay robustus is published by Perrichon et al. (2023).[54]
- A collection of eighteen isolated neosuchian teeth as well as a single isolated crocodyliform osteoderm are reported from the Berriasian–Valanginian Feliz Deserto Formation (Brazil) by Lacerda et al. (2023), who recognize a minimum of three morphotypes among the teeth.[55]
- A collection of 55 coprolites from the Eocene Na Duong Basin (Vietnam) are described by Halaçlar et al. (2023), who interpret them as belonging to a new ichnotaxon, Crococopros naduongensis [56]
Non-avian dinosaurs
[edit]New dinosaur taxa
[edit]Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Ampelognathus[57] | Gen. et sp. nov | Valid | Tykoski, Contreras & Noto | Late Cretaceous (Cenomanian) | Lewisville Formation | United States ( Texas) |
A small-bodied ornithopod. The type species is A. coheni. | |
Gen. et sp. nov |
Valid |
Simón & Salgado |
Late Cretaceous (Cenomanian) |
Huincul Formation |
A titanosaur sauropod. The type species is B. shiva. |
|||
Gen. et sp. nov |
Valid |
Prieto-Márquez & Sellés |
Late Cretaceous (Maastrichtian) |
A small-bodied ornithopod belonging to the group Styracosterna. The type species is C. rapidus. |
||||
Gen. et sp. nov |
Valid |
Agnolin et al. |
A colossosaurian titanosaur. The type species is C. diripienda. |
|||||
Gen. et sp. nov |
Ishikawa, Tsuihiji & Manabe |
Late Cretaceous (Campanian) |
A centrosaurine ceratopsid. The type species is F. elucidans. |
|||||
Gen. et sp. nov |
Mocho et al. |
Early Cretaceous (Barremian) |
A sauropod belonging to the group Somphospondyli. The type species is G. morellensis. |
|||||
Gen. et sp. nov |
Valid |
Alarcón-Muñoz et al. |
Late Cretaceous (Maastrichtian) |
A non-hadrosaurid hadrosauroid. The type species is G. nanoi. |
||||
Gremlin[64] | Gen. et sp. nov | Ryan et al. | Late Cretaceous (Campanian) | Oldman Formation | Canada ( Alberta) |
A leptoceratopsid ceratopsian. The type species is G. slobodorum. | ||
Gen. et sp. nov |
Valid |
Zanno et al. |
Late Cretaceous (Cenomanian) |
An iguanodontian ornithopod belonging to the group Rhabdodontomorpha. The type species is I. smithi. |
||||
Gen. et sp. nov |
Valid |
Gorscak et al. |
Late Cretaceous (Campanian) |
A titanosaur sauropod. The type species is I. semkhu. |
||||
Gen. et sp. nov |
In press |
Filippi et al. |
Late Cretaceous (Santonian) |
A titanosaur sauropod. The type species is I. oslatus. Announced in 2023; the final article version will be published in 2024. |
||||
Gen. et sp. nov |
Valid |
Kubo et al. |
Late Cretaceous |
A parvicursorine alvarezsaurid theropod. The type species is J. yaruui. |
||||
Gen. et sp. nov |
Valid |
Mo et al. |
Late Cretaceous (Maastrichtian) |
A titanosaur sauropod. The type species is J. ganzhouensis. |
||||
Gen. et sp. nov |
Valid |
Prieto-Márquez & Wagner |
Late Cretaceous (Campanian) |
A basally-branching hadrosaurid. Genus includes new species M. deckerti. Announced in 2022; the final article version was published in 2023. |
||||
Gen. et sp. nov |
In press |
Wang et al. |
Early Cretaceous |
A coelurosaurian theropod. The type species is M. laiyang. |
||||
Minimocursor[72] |
Gen. et sp. nov |
Valid |
Manitkoon et al. |
A basal member of Neornithischia. The type species is M. phunoiensis. |
||||
Oblitosaurus[73] | Gen. et sp. nov | Sánchez-Fenollosa, Verdú, & Cobos | Late Jurassic | Villar del Arzobispo Formation | Spain | An iguanodontian ornithopod belonging to the group Ankylopollexia. The type species is O. bunnueli. | ||
Gen. et sp. nov |
Valid |
Late Cretaceous (Maastrichtian) |
A pachycephalosaurid. The type species is P. clemensi. |
|||||
Gen. et sp. nov |
Valid |
Santos-Cubedo et al. |
Early Cretaceous (Barremian) |
A baryonychine spinosaurid theropod. The type species is P. cinctorrensis. |
||||
Gen. et sp. nov |
Valid |
Han et al. |
Early Jurassic (probably Sinemurian) |
A basal member of Sauropodomorpha. The type species is Q. shouhu. |
||||
Sphaerotholus lyonsi[77] | Sp. nov | Valid | Woodruff, Schott & Evans | Late Cretaceous (Campanian) | Dinosaur Park Formation | Canada ( Alberta) |
A pachycephalosaurine; a species of Sphaerotholus. | |
Sphaerotholus triregnum[77] | Sp. nov | Valid | Woodruff, Schott & Evans | Late Cretaceous (Maastrichtian) | Hell Creek Formation | United States ( Montana) |
A pachycephalosaurine; a species of Sphaerotholus. | |
Gen. et sp. nov |
Valid |
Bajpai et al. |
Middle Jurassic (Bathonian) |
A dicraeosaurid sauropod. The type species is T. indicus. |
||||
Gen. et sp. nov |
Valid |
Hattori et al. |
Early Cretaceous (Aptian) |
An ornithomimosaur theropod. The type species is T. fukuiensis. |
||||
Vectidromeus[80] | Gen. et sp. nov | In press | Longrich et al. | Early Cretaceous (Barremian) | Wessex Formation | United Kingdom | A hypsilophodontid. The type species is V. insularis. Announced in 2023; the final article version will be published in 2024. | |
Gen. et sp. nov |
Valid |
Pond et al. |
Early Cretaceous (Barremian) |
A nodosaurid. The type species is V. barretti. |
General non-avian dinosaur research
[edit]- Schwarz et al. (2023) observe the contents of unopened containers from Tendaguru Formation (Tanzania) expeditions via CT scans, and indicate the presence of fossils belonging to dinosaurs including Dysalotosaurus, Kentrosaurus, and Giraffatitan.[82]
- A study on causes of recovery of different interrelationships of the three major dinosaur clades (Theropoda, Sauropodomorpha, and Ornithischia) in phylogenetic studies is published by Černý & Simonoff (2023), who find the three possible ways of resolving the relationships among these lineages (Saurischia-Ornithischia, Ornithischiformes-Theropoda and Ornithoscelida-Sauropodomorpha dichotomies) to be statistically indistinguishable and supported by nearly equal numbers of characters in the datasets from the studies of Baron, Norman & Barrett (2017)[83] and Langer et al. (2017).[84][85]
- A review of the history of morphometric studies in non-avian dinosaurs is published by Hedrick (2023).[86]
- Cullen et al. (2023) reevaluate evidence for anomalously positive stable carbon isotope compositions of dinosaur bioapatite, report that the studied anomaly is present in the carbon isotope compositions of bioapatite in tooth enamel of not only dinosaurs but also mammals and crocodilians and in scale ganoine of gars from the "Rainy Day Site" in the Campanian Oldman Formation (Alberta, Canada) but is absent in extant vertebrates from the near-analogue modern ecosystem in the Atchafalaya Basin (Louisiana, United States), and interpret their findings as indicating that the studied anomaly is not the result of a unique dietary physiology of dinosaurs.[87]
- A study on the element ratios in the enamel of dinosaurs from the Oldman Formation is published by Cullen & Cousens (2023), who interpret their findings as indicative of differences in habitat use, dietary plant sources and feeding height between hadrosaurs and other ornithischians, as well as indicating that troodontid theropods were mixed-feeding to plant-dominant omnivores.[88]
- Dinosaur eggshell fragments with preserved eggshell membranes are reported from the Late Jurassic Brushy Basin Member of the Morrison Formation (Utah, United States) by Lazer et al. (2023).[89]
- Oussou et al. (2023) describe new tracksites with ornithopod, sauropod and theropod (including possible bird-like non-avian theropod) tracks from the Jurassic Isli Formation (Morocco).[90]
- Navarro-Lorbés et al. (2023) describe tracks produced by an undetermined bipedal non-avian dinosaur from the Lower Cretaceous Cameros Basin (Spain), interpreted as likely produced during swimming, and provide information on the swimming behaviour of the trackmaker.[91]
- Méndez Torrez et al. (2023) report the discovery of the first assemblage of dinosaur tracks (dominated by sauropod tracks, including tracks of possible non-neosauropod eusauropods, and possibly preserving evidence of herd behaviour) from the Jurassic to earliest Cretaceous Castellón Formation (Bolivia).[92]
- Naimi et al. (2023) describe tracks of small theropods and ornithopods from the Albian-Cenomanian strata from the Ouled Nail Mounts, representing some of the stratigraphically youngest records of non-avian dinosaurs in Algeria reported to date.[93]
- Esperante et al. (2023) report the discovery of a short-lived new site with hundreds of tracks of dinosaurs (subsequently removed because of the construction of a new road) from the El Molino Formation (Bolivia), including swim traces of theropod dinosaurs.[94]
- Description of four dinosaur teeth assignable to three different groups (Tyrannosauroidea, Titanosauriformes, and Hadrosauroidea) from the Cretaceous Sunjiawan Formation (China) is published by Yin et al. (2023), representing the first record of a theropod from the formation, as well as representing potentially two new taxa, as the hadrosauroid teeth are distinct from Shuangmiaosaurus.[95]
- A review of the Early Cretaceous dinosaur fauna from Thailand is published by Samathi et al. (2023).[96]
- Li et al. (2023) report the discovery of sauropod and ornithopod tracks from the Zonggei Formation, providing evidence for the presence of abundant dinosaurs in the Late Cretaceous of the Tibet region (China).[97]
- Flannery-Sutherland et al. (2023) describe the first dinosaur tracks from the Upper Cretaceous Nichkesaisk Formation (Kyrgyzstan), probably produced by both large-bodied and smaller-bodied theropods or ornithopods.[98]
- A study on the duration of Late Cretaceous megaherbivore dinosaur assemblage zones in the 100 m thick stratigraphic section exposed at Dinosaur Provincial Park (Alberta, Canada) is published by Eberth et al. (2023), who interpret their findings as indicating that the dinosaur assemblage zones in the studied section had duration time of ~600–700.000 years, and were significantly shorter than those in the overlying Horseshoe Canyon Formation.[99]
- Review of the Cretaceous non-avian dinosaur egg record from the Gobi Desert of Mongolia, including descriptions of eggs representing six ootaxa (Coralloidoolithus oosp., Dendroolithus oosp., Macroelongatoolithus oosp., Paraspheroolithus irenensis, cf. Protoceratopsidovum minimum, and cf. Spheroolithus maiasauroides) from the Upper Cretaceous localities Altan Uul I, Altan Uul IV, Bayanshiree, Shine Us Khudag and Shiluut Uul, is published by Tanaka et al. (2023).[100]
- A study on the stable oxygen and carbon isotope compositions of dinosaur eggshell calcites and tooth apatites from the Upper Cretaceous Kakanaut Formation (Chukotka Autonomous Okrug, Russia) is published by Amiot et al. (2023), who interpret their findings as indicating that near-polar Kakanaut dinosaurs likely laid eggs in early spring, giving time for the hatchlings to grow before winter.[101]
- A review of Cretaceous dinosaurs from India published by Khosla and Lucas (2023).[102]
Saurischian research
[edit]- An isolated ilium of a probable non-herrerasaurid herrerasaurian, potentially representing the first record of such a saurischian in unambiguous Carnian beds, is described from the Pivetta site (Candelária Sequence; Brazil) by Garcia et al. (2023).[103]
- Silva et al. (2023) described new herrerasaurid material from the Predebon site (Candelária Sequence of the Santa Maria Supersequence, Brazil), and interpret its anatomy as possibly indicative of the presence of a herrerasaurid morphotype distinct from Gnathovorax cabreirai and Staurikosaurus pricei.[104]
- A track site of dinosaur footprints is described from the Middle Jurassic Xietan Formation (Hubei, China) by Xing et al. (2023), who interpret the tracks as belonging to small sauropods (similar to Brontopodus) and probable theropods.[105]
- Lei et al. (2023) report theropod bite traces on 68 sauropod bones from the Upper Jurassic Morrison Formation (United States), as well as evidence of tooth wear in large-bodied theropods from the Morrison Formation interpreted as indicating that the studied theropods were biting into bone, and consider it most likely that the wear seen on large theropod teeth was mostly caused by contact with the destroyed bones of the more frequently consumed juvenile sauropods, while the studied bite traces were most likely caused by scavenging on carcasses of large-bodied sauropods.[106]
Theropod research
[edit]- A study on the developmental strategies underlying the evolution of body size of non-avialan theropods is published by D'Emic et al. (2023), who report that changes in the rate and duration of growth contributed nearly equally to the body size changes.[107]
- A study on the relationship between the body size of theropods, the area of muscles important for their balance and locomotion, and their capacity for agility is published by Henderson (2023), who argues that theropod body plan had an upper size limit based on a minimum acceleration threshold.[108]
- Cullen et al. (2023) use multiple lines of evidence, including histology of teeth and morphological comparisons, to evaluate proposed theropod facial reconstructions, and argue that non-avian theropods most likely had lips that covered their teeth.[109]
- Review of hand modifications and hand functions in late non-avian theropods is published by Barsbold (2023).[110]
- Kirmse et al. (2023) describe a coelophysoid femur from the Tytherington fissures near Bristol, UK, which cannot be definitively compared and referred to Pendraig.[111]
- Peng et al. (2023) describe abundant tracks from the Upper Triassic Tianquan track site (Xujiahe Formation; Ya'an, western Sichuan Basin, China), interpreted as produced by small theropods and representing one of the earliest record of dinosaurs from the eastern Tethys realm.[112]
- New specimen of Sinosaurus triassicus, including a complete skull and 11 cervical vertebrae, is described by Zhang, Wang & You (2023).[113]
- Purported "coelophysoid-grade" tibia from the Sinemurian of the Isle of Skye (Scotland, United Kingdom) is reinterpreted as fossil material of cf. Sarcosaurus woodi by Ezcurra et al. (2023).[114]
- Sharma, Hendrickx & Singh (2023) describe dental material of a non-coelurosaur averostran theropod from the Bathonian Fort Member of the Jaisalmer Formation (India), providing evidence of the presence of at least one taxon of a medium to large-bodied theropod on the Tethyan coast of India during the Middle Jurassic.[115]
- Tracks assigned to the ichnotaxon cf. Eubrontes, providing evidence of the presence of small theropods within the Hami pterosaur fauna, are described from the Lower Cretaceous Tugulu Group (Xinjiang, China) by Li et al. (2023).[116]
- Footprints of small theropods with a cursorial gait are described from the Lower Cretaceous Botucatu Formation (Brazil) by Leonardi et al. (2023), who name a new ichnotaxon Farlowichnus rapidus.[117]
- Theropod scrapes from the Cretaceous of Colorado, originally interpreted as evidence of display arenas or leks of theropods,[118] are argued to be more likely results of failed attempts by theropods to dig near-circular bowls that were to be used as nests by Moklestad & Lucas (2023).[119]
- Review of the fossil record of Abelisauroidea in continental Africa is published by Souza-Júnior et al. (2023).[120]
- Averianov & Lopatin (2023) describe an elongated and highly pneumatized cervical vertebra of a long-necked theropod from the Lower Cretaceous (Aptian) Ilek Formation (Kemerovo Oblast, Russia);[121] subsequently Averianov et al. (2024) interpret this vertebra as likely belonging to the holotype specimen of the noasaurid Kiyacursor longipes.[122]
- Barbosa et al. (2023) study the functional morphology of dental and pedal elements of the skeleton of Vespersaurus paranaensis, and interpret it as indicating that this theropod had a generalist diet, feeding on small or immobile prey.[123]
- Amudeo-Plaza et al. (2023) interpret a theropod tooth from the Cretaceous (Albian-Turonian) Quebrada La Totora Beds as the first record of an abelisaurid from Chile.[124]
- Paulina-Carabajal et al. (2023) report the discovery of a natural cranial endocast of an abelisaurid from the Santonian Bajo de la Carpa Formation (Argentina).[125]
- Longrich et al. (2023) describe new abelisaurid material from the Ouled Abdoun Basin, interpreted as indicative of coexistence of as many as three abelisaurid taxa in Morocco during the late Maastrichtian.[126]
- Description of the anatomy of the axial skeleton of Aucasaurus garridoi is published by Baiano et al. (2023).[127]
- A study on the evolution of the morphological characters of the pelvic girdle, femur, tibia and fibula in early theropods, especially in megalosauroids, is published by Lacerda, Bittencourt & Hutchinson (2023).[128]
- Lacerda, Bittencourt & Hutchinson (2023) present reconstructions of the hindlimb musculature of Condorraptor currumili, Marshosaurus bicentesimus and Piatnitzkysaurus floresi.[129]
- Revision of the spinosaurid taxonomy is published by Terras et al. (2023).[130]
- Pedal ungual phalanx of a possible spinosaurid is described from the Jurassic (Bathonian) Jaisalmer Formation (India) by Sharma, Novas & Singh (2023).[131]
- A collection of seven isolated spinosaurid teeth as well as a single preungual pedal phalanx of an indeterminate theropod are reported from the Berriasian–Valanginian Feliz Deserto Formation (Brazil) by Lacerda et al. (2023).[55]
- An isolated spinosaurid tooth of uncertain provenance, likely recovered from a Valanginian exposure of the Hastings Group (United Kingdom), is assigned to a taxon distinct from Baryonyx walkeri by Barker, Naish & Gostling (2023).[132]
- Barker et al. (2023) reconstruct the endocasts of the baryonychine spinosaurids Baryonyx walkeri and Ceratosuchops inferodios, finding their morphology to be similar to non-maniraptoriform theropods despite their highly modified skulls.[133]
- The first baryonychine teeth from South America reported to date are described from the Lower Cretaceous Feliz Deserto Formation (Brazil) by Lacerda et al. (2023).[134]
- Redescription of the anatomy of the skull of Irritator challengeri and a study on the affinities of this spinosaurid is published by Schade et al. (2023).[135]
- Description of a pathological tooth of Spinosaurus from the Late Cretaceous Ifezouane Formation (Morocco) is published by Smith and Martill (2023), representing the first record of external dental pathology in a spinosaurine spinosaurid.[136]
- Reconstruction of the musculature of the pectoral girdle and forelimbs in megaraptoran theropods is presented by Aranciaga Rolando et al. (2023).[137]
- A pathological third metatarsal of Phuwiangvenator, indicating that the bone experienced a greenstick fracture and healed before the animal's death, is described from the Lower Cretaceous Sao Khua Formation (Khon Kaen, Thailand) by Samathi et al. (2023).[138]
- A probable megaraptorid frontal and fused parietal fragment, representing the oldest megaraptorid skull element reported to date, is described from the Aptian upper Strzelecki Group (the "Wonthaggi Formation"; Australia) by Kotevski et al. (2023).[139]
- A study estimating the number of telencephalic neurons in theropod dinosaurs is published by Herculano-Houzel (2023), who argues that Allosaurus and Tyrannosaurus are endotherms with baboon- and monkey-like numbers of neurons;[140] however, this study has been criticized.[141][142]
- The study suggesting that carnosaurs like Allosaurus were primarily scavengers that fed on sauropod carcasses, originally published by Pahl and Ruedas (2021)[143] is criticized by Kane et al. (2023)[144] but later defended by Pahl and Ruehdas (2023).[145]
- Description of the endocranial anatomy of Allosaurus fragilis and A. jimmadseni is published by Lessner et al. (2023).[146]
- Yu et al. (2023) describe a probable metriacanthosaurid tooth from the Middle Jurassic Dongdaqiao Formation (China), interpret its morphological similarities to velociraptorine teeth as most likely resulting from convergent evolution, and argue that other Jurassic dromaeosaurid-like teeth from the Jurassic deposits of Asia and Europe might be teeth of non-dromaeosaurid theropods.[147]
- Carrano (2023) describes an incomplete theropod skeleton from the Lower Cretaceous Arundel Clay (Maryland, United States), representing the first definitive record of Acrocanthosaurus from the eastern part of North America reported to date.[148]
- Zhang et al. (2023) report the discovery of fossil downy feathers of coelurosaurs from the Lower Cretaceous Zhonggou Formation (China), with macromorphology (including rachis, barbs and barbules) essentially the same as in modern bird feathers, but with the microscopic morphology noticeably different from that of living bird feathers.[149]
- Johnson-Ransom et al. (2023) estimate bite force and cranial stresses in tyrannosauroid theropods, and interpret their findings as indicative of greater cranial stress and greater bite force in tyrannosaurids than in early-diverging tyrannosauroids.[150]
- Carr (2023) redescribes the hindlimb of the lectotype of Alectrosaurus olseni, describes a partial tyrannosauroid skull from the Iren Dabasu Formation (China) with similarities to skulls of Raptorex kriegsteini and juvenile Tyrannosaurus rex, and questions the assignment of fossil material from Mongolia and Uzbekistan to the genus Alectrosaurus.[151]
- Yun (2023) describes a tyrannosaurid pedal ungual from the Williams Fork Formation of Colorado (USA).[152]
- Therrien et al. (2023) describe a juvenile specimen of Gorgosaurus libratus from the Dinosaur Park Formation (Alberta, Canada), preserved with remains of two specimens of Citipes elegans within their first year of life in its abdominal cavity, and interpret this finding as indicating that G. libratus underwent a dietary shift over the course of its life.[153]
- New fossil material of Albertosaurus sarcophagus, including the left pubis with tooth traces interpreted as evidence of cannibalism, is described from the Danek Bonebed (Horseshoe Canyon Formation; Alberta, Canada) by Coppock & Currie (2023).[154]
- A study on the affinities of tyrannosaurines, reanalyzing the dataset of Warshaw & Fowler (2022),[155] is published by Scherer & Voiculescu-Holvad (2023), who name a new clade Teratophoneini, and find no support for a single anagenetic lineage within derived tyrannosaurines;[156] their findings are subsequently contested by Warshaw, Barrera Guevara & Fowler (2024), whose phylogenetic analysis indicates that recognized Daspletosaurus species represent a single anagenetic lineage ancestral to Tyrannosaurus-line tyrannosaurines.[157]
- Fiorillo et al. (2023) report the discovery of a theropod track from the Chignik Formation (Alaska, United States) produced by a tyrannosaur larger than Nanuqsaurus hoglundi, and interpret this finding as suggestive of different selective pressures on tyrannosaurids between the northern and southern extremes of Alaska.[158]
- Hodnett et al. (2023) report on a tyrannosaur tooth (assigned to cf. Tyrannosaurus sp.) from the Harebell Formation (Wyoming, United States), marking the first confirmed record of a dinosaur fossil discovered within the Yellowstone National Park.[159]
- Evidence of preservation of elements associated with bone remodeling and redeposition (sulfur, calcium, zinc) in a specimen of Tyrannosaurus rex, interpreted as indicative of preservation of original endogenous chemistry in the studied specimen, is presented by Anné et al. (2023).[160]
- A study on the formation and function of the enlarged unguals of alvarezsauroid and therizinosaur theropods is published by Qin et al. (2023), who interpret their findings as indicative of the evolution of digging adaptions in late-diverging alvarezsauroids, find the unguals of early-branching therizinosaurs to perform well in piercing and pulling, and interpret the enlarged unguals of Therizinosaurus as not adapted to functions that required considerable stress-bearing.[161]
- A study on the hindlimb variation between the best-preserved specimens of putative ornithomimosaurs from the Angeac-Charente bonebed (France) is published by Pintore et al. (2023), who interpret their findings as indicative of the presence of sexual dimorphism in the studied theropods.[162]
- Two ornithomimid pedal phalanges are described from the Late Cretaceous Fox Hills Formation (South Dakota, United States) by Chamberlain, Knoll, and Sertich (2023), representing the first dinosaur skeletal material from the formation.[163]
- Averianov et al. (2023) describe an ornithomimid tibia from the Maastrichtian Udurchukan Formation, (Amur Oblast, Russia), representing the first finding of an ornithomimid in the Upper Cretaceous strata from the Russian Far East reported to date.[164]
- A study on the bone histology of the holotype specimen of Parvicursor remotus is published by Averianov et al. (2023), who interpret this specimen as a young individual, not more than one year old, and reevaluate the course of alvarezsaurid miniaturization inferred by Qin et al. (2021),[165] finding no compelling morphological data indicating that parvicursorine alvarezsaurids fed on colonies of social insects and that their miniaturization was related to myrmecophagy.[166]
- A study on the range of motion at the shoulder in Mononykus olecranus is published by Senter (2023).[167]
- Wills, Underwood & Barrett (2023) identify therizinosauroid and troodontid teeth, as well as three morphotypes of dromaeosaurid teeth, in a sample of isolated theropod teeth from the Middle Jurassic (Bathonian) microvertebrate sites in the United Kingdom.[168]
- Reconstruction of the hindlimb musculature of Falcarius utahensis is presented by Smith (2023).[169]
- Smith & Gillette (2023) reconstruct soft tissues of the hindlimbs and likely posture of Nothronychus graffami.[170]
- Skeletal indicators of a propatagium are investigated by Uno & Hirasawa (2023), supporting the presence of this structure in non-avian pennaraptorans such as Caudipteryx and Microraptor.[171]
- A review of the evidence for partially buried eggs and their significance for the evolution of contact incubation in Mesozoic pennaraptorans is published by Hogan & Varrcchio (2023).[172]
- Averianov & Lopatin (2023) describe fossil material (metatarsals) of a caenagnathid with similaries to Elmisaurus rarus and a dromaeosaurid with similarities to Velociraptor mongoliensis from the Upper Cretaceous Bostobe Formation (Kazakhstan).[173]
- Voris, Zelenitsky & Therrien (2023) describe new caenagnathid fossil material from the upper Maastrichtian portion of the Scollard Formation (Alberta, Canada), including fossils indicative of the presence of a large-bodied taxon similar to Anzu wyliei or Caenagnathus collinsi.[174]
- The most complete caenagnathid specimens from the southern part of North America reported to date are described from the Campanian Aguja Formation (Texas, United States) by Wick, Lehman & Fortner (2023), who present a histology-based growth model for one of the studied specimens (the first for a caenagnathid), indicating that it needed least five years to approach fully adult size.[175]
- The feasibility of contact incubation by oviraptorids based on their nest architecture is experimentally tested by Hogan (2023).[176]
- A review of bone microstructure and histology in dromaeosaurids and troodontids is published by Martin, Currie & Kundrát (2023).[177]
- Yang et al. (2023) report the first discovery of fossil materials of a large-bodied dromaeosaurid (probably a eudromaeosaur) from the Upper Cretaceous Quantou Formation (Jilin, China).[178]
- Croudace et al. (2023) reconstruct the feather colouration of an approximately one-year-old individual of Wulong bohaiensis, reporting evidence indicative of the presence of iridescent plumage of the forelimb and hindlimb remiges and grey plumage on other portions of the body.[179]
- A partial left tibia and articulated proximal tarsals, likely belonging to an indeterminate velociraptorine, are described from the Upper Cretaceous Lo Hueco fossil site (Cuenca, Spain) by Malafaia et al. (2023), who also review the European theropods of the Late Cretaceous.[180]
- Averianov & Lopatin (2023) describe new fossil material of Kansaignathus sogdianus from the Santonian Ialovachsk Formation (Tajikistan), and confirm the phylogenetic placement of K. sogdianus as the basalmost Asiatic velociraptorine.[181]
- Czepiński (2023) describes a specimen of Shri devi with a partial skull from the Upper Cretaceous Barun Goyot Formation (Mongolia), and reports that the anatomy of the skull confirms close affinities of Shri with Velociraptor mongoliensis, but also that the skull has anatomical features suggesting convergence to the North American eudromaeosaurians.[182]
- A study on the nasal structures of Velociraptor mongoliensis, indicating that this theropod was unlikely to have a fully developed nasal thermoregulation apparatus for its brain as seen in modern birds, is published by Tada et al. (2023).[183]
- A study on the bone histology of the holotype of Liaoningvenator curriei is published by Martin, Caizhi & Kundrát (2023), who interpret their findings as indicative of a growth pattern transitive between those of basalmost and more derived troodontids.[184]
- Evidence from eggshells of Troodon, interpreted as indicative of endothermic physiology but also of reptile-like eggshell mineralization process, is presented by Tagliavento et al. (2023).[185]
Sauropodomorph research
[edit]- Lockley et al. (2023) evaluate a number of trackways assigned to basal saurischians, including those belonging to the ichnogenera Otozoum, Pseudotetrasauropus, Evazoum, and Kalosauropus, and examine their implications on the gait of "prosauropods".[186]
- A new specimen of Buriolestes schultzi, interpreted as stouter than other specimens of B. schultzi and providing evidence of previously unknown variation in robustness within this species, is described from the Late Triassic of southern Brazil by Moro et al. (2023).[187]
- A study on sauropodomorph tracks from the Upper Triassic lower Elliot Formation (Lesotho) is published by Sciscio et al. (2023), who interpret the studied tracks as confirming that sauropodomorphs already evolved large body size by the Norian, but also indicating that the makers of the studied tracks used both bipedal and quadrupedal locomotion styles during a 10-million-years interval in the Norian.[188]
- Chapelle, Botha & Choiniere (2023) study the histology of a small sauropodomorph humerus from the upper Elliot Formation (South Africa), and interpret this specimen as a bone of a skeletally mature individual of a new taxon with a body mass of approximately 75.35 kg, representing the smallest known Jurassic sauropodomorph reported to date.[189]
- New information on the anatomy of Jaklapallisaurus asymmetricus is presented by Ezcurra et al. (2023), who interpret J. asymmetricus as a member of Unaysauridae.[190]
- Müller et al. (2023) describe the remains of a juvenile specimen of Unaysaurus, found associated with the holotype, from the Late Triassic Caturrita Formation (Brazil).[191]
- Taxonomic revision of basal sauropodomorph specimens stored in the Palaeontological Collection of Tübingen, historically referred to the genus Plateosaurus, is published by Regalado Fernandez et al. (2023).[192]
- Aureliano et al. (2023) provide evidence of the presence of an invasive air sac system in Macrocollum itaquii.[193]
- Bem & Müller (2023) report the first discovery of the fossil material of Macrocollum itaquii outside its type locality.[194]
- Moopen et al. (2023) describe material of a probable lessemsaurid from the Triassic lower Elliot Formation and estimating it to be one of the largest sauropodomorphs from the Norian of South Africa, as well as the first plant-vertebrate fossil associations in the formation.[195]
- A study on the evolution of sauropod body mass is published by D'Emic (2023), who finds that sauropods independently surpassed the maximum body mass of terrestrial mammals at least three dozen times in their evolutionary history.[196]
- Description of the anatomy of a partial juvenile sauropod vertebral series from the Middle Jurassic Nam Phong Formation (Thailand), interpreted as indicative of non-eusauropod affinities of the studied specimen, is published by Hanta et al. (2023).[197]
- Description of new eusauropod fossil material from the Middle Jurassic Dongdaqiao Formation (China) is published by Wei et al. (2023), who interpret these findings as showing that gigantic sauropods were more widespread than previously known during the Middle Jurassic.[198]
- A juvenile sauropod specimen, most closely resembling early-diverging eusauropods from the Middle Jurassic but sharing some derived features with the Late Jurassic mamenchisaurids and neosauropods, is described from the Middle Jurassic Dongdaqiao Formation (East Tibet, China) by An et al. (2023).[199]
- The holotype of Mamenchisaurus sinocanadorum is redescribed by Moore et al. (2023), who also interpret Bellusaurus and Daanosaurus as juvenile mamenchisaurids.[200]
- A tooth of a possible member of Turiasauria, which might represent the oldest record of the group reported to date, is described from the Lower Jurassic (Pliensbachian) Halse Formation (Denmark) by Milàn & Mateus (2023).[201]
- A study on the anatomy of the skull of Bajadasaurus pronuspinax is published by Garderes et al. (2023).[202]
- A study on bifurcated cervical ribs in apatosaurines is published by Wedel & Taylor (2023), who interpret the studied structures as divergent muscle attachments, likely enabling improved muscular control in the middle of the neck.[203]
- A rebbachisaurid vertebra from the La Amarga Formation (Argentina) is redescribed by Lerzo (2023), who finds it to be a derived member of Rebbachisaurinae.[204]
- A study on the microanatomy of the long bones of Nigersaurus taqueti is published by Lefebvre, Allain & Houssaye (2023), who interpret their findings as indicating that microanatomical structure in sauropod limb bones was not subject to drastic selective pressures imposed by heavy weight-bearing.[205]
- New rebbachisaurid specimen, providing new information on the anatomy of the hindlimbs of rebbachisaurids, is described from the Cenomanian Huincul Formation (Argentina) by Bellardini et al. (2023).[206]
- Torcida Fernández-Baldor et al. (2023) describe a dentary and several teeth of a basal macronarian close to Camarasaurus from the Valdepalazuelos site (Rupelo Formation; Spain) living during the Tithonian–Berriasian transition, providing evidence of the presence of two macronarian taxa at the Valdepalazuelos site.[207]
- Cervical vertebra representing the first record of a titanosauriform sauropod from the Lower Cretaceous Kanmon Group (Japan) is described by Tatehata, Mukunoki & Tanoue (2023).[208]
- Sauropod fossil material, including a vertebra of a possible member of the genus Ornithopsis, is described from the Lower Cretaceous sediments from the Balve II locality (Germany) by Hornung, Sachs & Schwermann (2023), representing the first finding of sauropod fossils from the upland environment in Europe reported to date.[209]
- New information on the pneumatization of the ribs of the holotype specimen of Brachiosaurus altithorax is presented by Taylor & Wedel (2023).[210]
- Lim et al. (2023) report the discovery of a fibula of a member of the family Euhelopodidae from the strata of the Lower Cretaceous Grès supérieurs Formation at Koh Paur island, representing the first finding of a non-avian dinosaur from Cambodia reported to date.[211]
- Cruzado-Caballero et al. (2023) describe two new cases of caudal pathology in titanosaurs from the Late Cretaceous of Argentina and evaluate these cases for interpreting the commonness of pathology occurring in the fossil record.[212]
- The pneumaticity of a titanosaur specimen from the Black Peaks Formation (Texas, United States) is investigated by Fronimos (2023).[213]
- Averianov et al. (2023) describe a series of caudal vertebrae representing the first sauropod material from the Shestakovo 3 locality from the Lower Cretaceous Ilek Formation (Kemerovo Oblast, Russia), and interpret it as new fossil material of Sibirotitan astrosacralis.[214]
- New specimen of Diamantinasaurus matildae, including the skull preserving cranial elements not previously known for this taxon and showing similarities with the skull of Sarmientosaurus musacchioi, is described from the Upper Cretaceous Winton Formation (Australia) by Poropat et al. (2023).[215]
- Titanosaur teeth representing three distinct morphotypes, including the largest titanosaur tooth ever found, are described from the Upper Cretaceous Serra da Galga Formation (Brazil) by Silva Junior et al. (2023).[216]
- Dhiman et al. (2023) report the discovery of 92 titanosaur egg clutches from the Upper Cretaceous Lameta Formation (Madhya Pradesh, India), including three types of clutches and assigned to six oospecies, interpret their findings as suggestive of higher diversity of titanosaur taxa from the Lameta Formation than indicated by body fossils, and evaluate the implications of the studied egg clutches for the knowledge of the reproductive biology of titanosaurs.[217]
- A study on the bone histology of Uberabatitan ribeiroi, providing evidence of rapid, uninterrupted growth that ceased with the appearance of periodic interruptions in the advanced stages of development, is published by Windholz et al. (2023).[218]
- A study on the long bone histology of Muyelensaurus pecheni and Rinconsaurus caudamirus is published by González et al. (2023), who find no evidence of a correlation between the ontogenetic stage and the body size in both taxa, unlike in other neosauropods.[219]
- A new sauropod specimen (a saltasaurid humerus) is described from the Campanian deposits from the Quseir Formation (Egypt) by Wahba et al. (2023).[220]
- A sauropod tooth assigned to the family Opisthocoelicaudiidae, representing the first record of a sauropod from Late Cretaceous Russia, is described from the Udurchukan Formation, (Russia) by Averianov, Bolotsky, and Bolotsky (2023).[221]
- Paul and Larramendi (2023) suggest that some sauropods reached sizes comparable to the largest whales, and propose that the fragmentary taxon Bruhathkayosaurus may have weighed between 110 and 170 tonnes.[222]
- Multiple sauropod tracks assigned to cf. Brontopodus isp., providing the first ichnological evidence of gregarious behavior in Cretaceous sauropods in Africa, are described from the Lower Formation of the Cenomanian Djoua series in the In Amenas region of Algeria by Zaagane et al. (2023).[223]
Ornithischian research
[edit]- A study on the biomechanical properties of the skulls of Heterodontosaurus tucki, Lesothosaurus diagnosticus, Scelidosaurus harrisonii, Hypsilophodon foxii and Psittacosaurus lujiatunensis is published by Button et al. (2023), who interpret their findings as indicative of limited functional convergence among studied taxa, which achieved comparable performance of the feeding apparatus through different adaptations.[224]
- A study on the evolution of forelimb muscle mechanics and function in ornithischian dinosaurs is published by Dempsey et al. (2023), who interpret their findings as indicating that thyreophorans, ornithopods and ceratopsians evolved quadrupedality through different patterns of rearrangement of forelimb musculature.[225]
- Review of the fossil record of ornithischian dinosaurs from Southeast Asia and southern China is published by Manitkoon et al. (2023)[226]
- Surmik et al. (2023) study ossified tendons of specimens of Pinacosaurus grangeri, Edmontosaurus regalis/"Ugrunaaluk kuukpikensis" and Homalocephale calathocercos, reporting the presence of collagenous fibre bundles and likely fibril bundles, blood vessels and associated cells in some of the studied samples, and argue that ossified tendons can be a source of molecular preservation in dinosaurs.[227]
- A study on the histology and enamel microstructure of the maxillary cheek teeth of Heterodontosaurus tucki, providing the earliest known evidence of the presence of wear-resistant modified dentine in an ornithischian, is published by Calvert et al. (2023).[228]
- Description of the skull osteology of Manidens condorensis is published by Becerra et al. (2023).[229]
- Button & Zanno (2023) present a three-dimensional endocranial reconstruction of a specimen of Thescelosaurus neglectus, and report the presence of brain traits interpreted as suggestive of cognitive and behavioral capabilities within the range of extant reptiles, as well as a narrow hearing range, acute olfaction and vestibular sensitivity which might represent adaptations for burrowing behaviors.[230]
Thyreophoran research
[edit]- A study on the phylogenetic relationships of thyreophorans is published by Raven et al. (2023), who identify four distinct ankylosaur clades, with the long-standing clade Nodosauridae recovered as paraphyletic; they suggest replacing the latter with the names Panoplosauridae, Polacanthidae, and Struthiosauridae.[231]
- A study on the use of quadrapediality in Scutellosaurus lawleri, and on its implications for locomotor behavior evolution in dinosaurs, is published by Anderson et al. (2023), who interpret Scutellosaurus as mainly being a biped, and suggest quadrapediality was used during specific activities.[232]
- Galton (2023) describes a right sternal bone of a specimen of Stegosaurus from the Carnegie Quarry at Dinosaur National Monument (Morrison Formation; Utah, United States) and reevaluates three putative sternal bones from Como Bluff (Wyoming, United States) described by Gilmore (1914),[233] arguing that they are neither sternal bones nor fossils of Stegosaurus.[234]
- Description of nodosaurid osteoderms from the Late Cretaceous Snow Hill Island Formation (Antarctica) is published by Brum et al. (2023), who suggest that osteoderm structure may have helped nodosaurids colonize high-latitude environments more easily.[235]
- Yoshida, Kobayashi & Norell (2023) report the discovery of fossilized larynx of a specimen of Pinacosaurus grangeri from the Campanian of Ukhaa Tolgod (Mongolia), and interpret its anatomy as indicating that Pinacosaurus might have been capable of vocalization and, like extant birds, might have possessed a non-laryngeal vocal source and used larynx as a sound modifier.[236]
- Tumanova et al. (2023) describe anomalies within the airway and sinuses of a skull of a specimen of Tarchia, which were only detected while CT scanning the specimen, and which might have been caused by infection and/or trauma.[237]
- A study on the cranial biomechanics of Panoplosaurus mirus and Euoplocephalus tutus is published by Ballell, Mai & Benton (2023), who find evidence of differences interpreted as indicative of relatively higher bite forces in Panoplosaurus, as well as indicative of stronger reinforcement of the skull of Euoplocephalus, consistent with highly defensive function.[238]
Cerapod research
[edit]- Evidence of significantly rougher dental microwear texture in Late Cretaceous ornithopods compared to earlier members of the group, interpreted as indicative of dietary shift towards more abrasive foodstuffs, is presented by Kubo et al. (2023).[239]
- Review of the diversity, relationships, biogeography and paleoecology of rhabdodontids is published by Augustin, Ősi & Csiki-Sava (2023).[240]
- New rhabdodontid fossil material, possibly representing a taxon distinct from known Transylvanian rhabdodontids, is described from the Maastrichtian Densuș-Ciula Formation (Hațeg Basin; Romania) by Magyar et al. (2023).[241]
- Redescription of Cumnoria prestwichii is published by Maidment et al. (2023), who recover Cumnoria as a non-ankylopollexian iguanodontian, and consider it to be distinct from Camptosaurus.[242]
- Rotatori et al. (2023) report the presence of a rich neurovascular network in the dentary of a dryosaurid from the Upper Jurassic Lourinhã Formation (Portugal), similar to vascularisation present in cerapodan dinosaurs with high tooth replacement rates.[243]
- Redescription of the holotype of Mantellisaurus atherfieldensis is published by Bonsor et al. (2023), who confirm Mantellisaurus to be distinct from Iguanodon.[244]
- García-Cobeña, Cobosa & Verdú (2023) describe bone and trace fossils of styracosternan ornithopods from the Lower Cretaceous El Castellar Formation and Camarillas Formation (Spain), including manus-pes track set from the Camarillas Formation indicative of quadrupedal locomotion, assigned to the ichnogenus Caririchnium and produced by large styracosternans related to Iguanodon.[245]
- A study on the palynological sample from the matrix surrounding a specimen of Iguanodon bernissartensis from the new Palau-3 site in the Lower Cretaceous Morella Formation is published by Rodríguez-Barreiro et al. (2023), who interpret the studied specimen as living in a coastal open forest environment with a warm and humid climate; the authors also compare the habitat of the studied specimen with those from other I. bernissartensis-bearing sites, and interpret I. bernissartensis as feeding mostly on fronds of ferns belonging to the families Anemiaceae and Cyatheaceae, as well as on the foliage of members of the family Cheirolepidiaceae.[246]
- A study on the evolution of the dentary in hadrosauroids, providing evidence of changes during the transition from non-hadrosaurid hadrosauroids to saurolophids which probably enhanced food gathering and food processing abilities, is published by Söderblom et al. (2023).[247]
- Description of new hadrosaurid fossils from the Upper Cretaceous Kakanaut Formation (Chukotka, Russia) and a study on their histology is published by Bapinaev et al. (2023), who interpret the studied fossils as possibly indicative of the presence of two hadrosaurid taxa in the Kakanaut fauna, and interpret the histology of the studied bones as possibly indicating that Arctic hadrosaurids of Chukotka were year-round residents of polar ecosystems.[248]
- Joubarne, Therrien & Zelenitsky (2023) describe extensive skin impressions in three hadrosaurid specimens from the Campanian Dinosaur Park Formation (Alberta, Canada), with two specimens preserving integument of the manus showing that their digits II–III–IV were approximately equal in length and united in a common fleshy structure, and the third specimen preserving scale stripes on its torso which might have corresponded to color stripes in life.[249]
- A study on the cranial suture interdigitation in Hadrosaurids, using data gathered from Gryposaurus and Corythosaurus is published by Dudgeon and Evans (2023) who find that suture interdigitation increased across Hadrosaurid ontogeny, that Lambeosaurines had higher suture interdigitation than other Iguanodontians, and that increased suture complexity coincided with Lambeosaurine crest evolution.[250]
- Currie, Lü & Wang (2023) describe the maxilla of a juvenile lambeosaurine (likely either Corythosaurus or Lambeosaurus) from the Campanian Dinosaur Park Formation (Alberta, Canada), compare it with the maxilla of a probable juvenile hadrosaurine (possibly Gryposaurus) from a different bonebed from the same formation, and interpret these fossils as indicating that lambeosaurines and hadrosaurines had similar tooth counts at hatching, which subsequently diverged during ontogeny.[251]
- Description of the anatomy of the postcranial skeleton of Laiyangosaurus youngi is published by Zhang et al. (2023).[252]
- Seymour et al. (2023) estimate blood flow rates to the tibia shafts of Maiasaura peeblesorum, and report higher flow rates in juveniles which were likely related to higher oxygen demand for bone growth in juveniles compared to maintenance and repair of bone tissue damage in adults.[253]
- A study on the anatomy of the holotype specimen of Gravitholus albertae is published by Dyer, Powers & Currie (2023), who interpret both Gravitholus albertae and Hanssuesia sternbergi as likely junior synonyms of Stegoceras validum.[254]
- Han et al. (2023) describe entangled specimens of Psittacosaurus lujiatunensis and Repenomamus robustus from the Lujiatun Member of the Yixian Formation (China), and interpret the studied specimens as likely locked in combat as a result of the predation attempt on the part of the mammal.[255]
- A study on the endocranial morphology of Liaoceratops yanzigouensis is published by Yang et al. (2023), who find that the brain, olfactory bulb and inner ear of Liaoceratops more closely resemble those observed in Psittacosaurus than those in more derived ceratopsians.[256]
- A review of the cranial evolution in Ceratopsia is published by Nabavizadeh (2023).[257]
- Chiba et al. (2023) provide evidence of the presence of frill margin undulations in Protoceratops andrewsi, and interpret the undulated frill margin as possible shared feature in protoceratopsids or even Coronosauria.[258]
- Berry (2023) interprets the fossil record of late Campanian ceratopsids from western North America as indicative of a significant rate of background extinction approximately 76 million years ago, and interprets this pattern as most likely caused by competition for shared resources by sympatric ceratopsid species.[259]
- The development and homology of epiparietals (P1 and P2) in three Centrosaurus specimens are described by Mallon, Holmes & Rufolo (2023), who suggest that these are separate ossifications that fuse with the parietal at different stages of ontogeny.[260]
- A study on the bone histology of Triceratops, providing evidence of a relatively fast and continuous growth rate, is published by de Rooij et al. (2023).[261]
- A study on the range of shoulder motion and on the orientation of the long bones of the forelimb of Thescelosaurus and Styracosaurus is published by Senter & Mackey (2023).[262]
Birds
[edit]New bird taxa
[edit]Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Anachronornis[263] | Gen. et sp. nov. | Valid | Houde, Dickson & Camarena | Thanetian | Willwood Formation | United States ( Wyoming) |
A basal anseriform of the new family Anachronornithidae. The type species is A. anhimops. | |
Sp. nov |
Valid |
Mayr & Kitchener |
Eocene |
A member of the family Vastanavidae. |
||||
Gen. et comb. nov |
Valid |
Zelenkov |
Miocene |
A duck; a new genus for "Anas" natator Milne-Edwards (1867). |
||||
Gen. et sp. nov |
Buffetaut, Angst & Tong |
Late Cretaceous (probably late Campanian) |
Argiles et Grès à Reptiles Formation |
A member of Enantiornithes. The type species is C. sebei. |
||||
Gen. et sp. nov |
Valid |
Mayr & Kitchener |
Eocene |
London Clay |
A member of Charadriiformes most closely resembling members of the group Charadrii. The type species is C. essexensis. |
|||
Gen. et sp. nov |
Valid |
Mayr et al. |
Paleocene |
A member of the stem group of Phaethontiformes. The type species is C. novaezealandicum. |
||||
Gen. et sp. nov |
Valid |
Li et al. |
A non-ornithothoracine pygostylian. The type species is C. zhui. |
|||||
Danielsavis[263] | Gen. et sp. nov. | Valid | Houde, Dickson & Camarena | Ypresian | London Clay Formation | United Kingdom | A member of Galloanseres of uncertain affinities; originally described as a basal anseriform, but subsequently argued to share possible derived characteristics with the Galliformes by Mayr, Carrió & Kitchener (2023).[270] The type species is D. nazensis. | |
Dynatoaetus[271] | Gen. et 2 sp. nov. | Valid | Mather et al. | Chibanian | Mairs Cave | Australia | An Accipitrid, the type species is D. gaffae. It also includes the species D. pachyosteus.[272] | |
Gen. et sp. nov |
Valid |
Mayr, De Pietri & Kitchener |
Eocene (Ypresian) |
London Clay |
A trogon. The type species is E. stenorhynchus. |
|||
Sp. nov |
Valid |
Thomas et al. |
Pliocene (Piacenzian) |
A penguin, a species of Eudyptula. |
||||
Sp. nov |
Valid |
Emslie & Mead |
Late Quaternary |
A kestrel. |
||||
Fujianvenator[276] | Gen. et sp. nov. | Valid | Xu et al. | Late Jurassic (Tithonian) | Nanyuan Formation | China | An anchiornithid. The type species is F. prodigiosus. | |
Sp. nov |
Valid |
Ksepka et al. |
Paleocene (Teurian) |
An early penguin. |
||||
Gen. et sp. nov |
Valid |
Bocheński et al. |
Miocene |
A duck. The type species is L. hassleri. |
||||
Sp. nov |
Valid |
Tennyson & Salvador |
Pliocene (Waipipian) |
A member of the genus Macronectes. |
||||
Sp. nov |
Valid |
Zelenkov |
Miocene |
A duck. |
||||
Sp. nov |
Valid |
Zelenkov |
Miocene |
A duck. |
||||
Murgonornis[281] | Gen. et sp. nov | Worthy et al. | Eocene | Australia | A presbyornithid. The type species is M. archeri | |||
Ssp. nov |
Valid |
Holocene |
A subspecies of Abbott's booby. |
|||||
Gen. et sp. nov |
In press |
Mourer-Chauviré et al. |
Eocene (Ypresian) |
A bird classified as cf. Aramidae. The type species is P. annae. |
||||
Pelecanus paranensis[284] | Sp. nov | Noriega et al. | Miocene | Paraná Formation | Argentina | A pelican. | ||
Sp. nov |
Valid |
Mayr, Carrió & Kitchener |
Eocene (Ypresian) |
London Clay |
Possibly a relative of bustards, assigned to the family Perplexicervicidae. |
|||
Gen. et sp. nov |
Valid |
Ksepka et al. |
Paleocene (Teurian) |
Moeraki Formation |
An early penguin. The type species is P. stonehousei. |
|||
Sp. nov |
Valid |
Ksepka et al. |
Miocene (Aquitanian) |
Mount Harris Formation |
A member of Pan-Diomedeidae. |
|||
Porzana payevskyi[286] |
Sp. nov |
Valid |
Zelenkov et al. |
Early Pleistocene |
A rail; a species of Porzana. |
|||
Gen. et sp. nov |
Valid |
Kessler & Horváth |
Oligocene |
A cormorant. The type species is P. strigoniensis. |
||||
Pterocles bosporanus[288] | Sp. nov | Zelenkov | Pleistocene | Crimea | A sandgrouse; a species of Pterocles. | |||
Sp. nov |
Mayr & Kitchener |
Eocene |
London Clay |
A member of the family Halcyornithidae. |
||||
?Pulchrapollia tenuipes[289] |
Sp. nov |
Mayr & Kitchener |
Eocene |
London Clay |
A member of the family Halcyornithidae. |
|||
Sp. nov |
Valid |
Mayr & Kitchener |
Eocene (Ypresian) |
London Clay |
A member of the family Threskiornithidae. |
|||
Gen. et sp. nov |
Valid |
Zelenkov |
Miocene |
A duck. Genus includes new species S. lacustrina. |
||||
Gen. et sp. nov |
Valid |
Nguyen |
Oligocene |
A bowerbird. The type species is S. marynguyenae. |
||||
Sibirionetta formozovi[286] |
Sp. nov |
Valid |
Zelenkov et al. |
Early Pleistocene |
A duck; a species of Sibirionetta. |
|||
Sororavis[292] | Gen. et sp. nov | Valid | Mayr & Kitchener | Eocene (Ypresian) | London Clay | United Kingdom | A member of the family Morsoravidae. The type species S. solitarius. | |
Gen. et sp. nov |
Valid |
Zelenkov |
Miocene |
A duck. Genus includes new species T. palaeobaikalensis. |
||||
Gen. et sp. nov |
In press |
Mourer-Chauviré et al. |
Eocene (Ypresian) |
A bird classified as cf. Galliformes. The type species is T. corbalani. |
||||
Sp. nov |
Valid |
Agnolín |
Late Miocene (Tortonian) |
A member of the family Falconidae. |
||||
Titanoperdix[286] |
Gen. et sp. nov |
Valid |
Zelenkov et al. |
Early Pleistocene |
A phasianid. The type species is T. felixi. |
|||
Sp. nov |
Valid |
Mayr & Kitchener |
Eocene |
London Clay |
A member of the family Messelasturidae. |
|||
Tynskya crassitarsus[264] |
Sp. nov |
Valid |
Mayr & Kitchener |
Eocene |
London Clay |
A member of the family Messelasturidae. |
||
Sp. nov |
Degrange et al. |
Pliocene |
||||||
Yarquen[295] | Gen. et sp. nov | Tambussi et al. | Miocene | Collón Curá Formation | Argentina | An owl in the family Strigidae. The type species is Y. dolgopolae. | ||
Gen. et sp. et comb. nov |
Valid |
Mayr & Kitchener |
Early Eocene |
London Clay |
An owl. The type species is Y. michaeldanielsi; genus also includes "Eostrix" gulottai Mayr (2016). Announced in 2022; the final article version was published in 2023. |
Avian research
[edit]- A study on the evolution of limbs along avialan stem lineages is published by Wang & Zhou (2023), who provide evidence of a shift to low disparity and decelerated evolutionary rates near the origin of avialans, and interpret this shift as related to the evolutionary constrains on the morphology of the forelimb necessary for powered flight.[297]
- Macaulay et al. (2023) report that, in spite of the differences of body shape, there is overall no difference in the position of whole-body centre-of-mass between birds and non-avian theropods, but rather that there is such difference between hindlimb-dominated predominantly terrestrial taxa and forelimb-dominated predominantly volant taxa regardless of their phylogenetic placement, and argue that the fully crouched bipedalism seen in modern birds evolved after powered flight.[298]
- A study comparing dentin and enamel microstructure in Microraptor, Anchiornis, Sapeornis and Longipteryx, providing evidence of microscopic modifications in tooth enamel, dentin and cementum between early birds and other theropods, as well as previously unrecognized plasticity in the developmental mechanisms controlling tooth microstructure in Mesozoic toothed birds, is published by Wang et al. (2023).[299]
- Kiat & O'Connor (2023) reevaluate evidence of molt in the fossil record of birds and non-avian dinosaurs, report rarity of molt occurrence both in the fossil record and in collections of extant bird species with simultaneous molts, and argue that the flight feather annual molt evolved with the development of powered flight, possibly only among crown birds.[300]
- Hong et al. (2023) describe a footprint assigned to the ichnospecies Wupus agilis from the Cretaceous Daegu Formation, representing the largest bird footprint from South Korea described to date, report that ichnotaxa intermediate between non-avian theropod and unwebbed Mesozoic bird ichnotaxa generally show high morphological similarity with bird ichnospecies, and argue that these intermediate ichnotaxa might represent the ichnological record of large Mesozoic birds.[301]
- The oldest bird tracks from Gondwana reported to date are described from the Lower Cretaceous "Wonthaggi Formation" (Australia) by Martin et al. (2023).[302]
- Wu et al. (2023) study the phytoliths preserved in the stomach contents of a specimen of Jeholornis prima, interpreting them as indicating that Jeholornis likely ate leaves of plants from the magnoliid angiosperm clade.[303]
- Five specimens of Sapeornis chaoyangensis with different-preserved feathers are reported from the Early Cretaceous Jehol Biota (China) by Zhao et al. (2023), who examine their implications for the taphonomy of soft tissues from the Jehol Biota.[304]
- Evidence from the study of well-preserved specimen of Confuciusornis sanctus, interpreted as indicating that this bird was capable of prolonged flights as long as it alternated periods of high-efficiency gliding with active flapping, is presented by Chiappe et al. (2023).[305]
- An enantiornithine specimen from the Lower Cretaceous La Huérguina Formation closely resembling Concornis is described by Nebreda et al. (2023).[306]
- O'Connor et al. (2023) describe feathers of a young enantiornithine individual from the Cretaceous amber from Myanmar, and interpret this finding as indicating that immature enantiornithines rapidly molted body feathers.[307]
- Redescription and a study on the affinities of Dapingfangornis sentisorhinus is published by Wang et al. (2023).[308]
- A study aiming to determine the diets of members of the family Pengornithidae is published by Miller et al. (2023), who report that Pengornis, Parapengornis and Yuanchuavis show adaptations for vertebrate carnivory.[309]
- Wang (2023) describes a new specimen of Parabohaiornis martini with a well-preserved skull from the Lower Cretaceous Jiufotang Formation (China), and reports the presence of the plesiomorphic temporal and palatal configurations (similar to those of non-avian dinosaurs) in the skull of Parabohaiornis.[310]
- Clark et al. (2023) attempt to determine the dietary habits of longipterygids, reporting dental features indicative of carnivory, with additional support for insectivory.[311]
- A study on the gastral mass preserved with specimens of Archaeorhynchus and Iteravis, interpreted as indicative of the digestive system comparable to that of extant birds, is Liu et al. (2023).[312]
- Lowi-Merri et al. (2023) provide evidence of soaring and foot-propelled swimming capabilities of Ichthyornis.[313]
- Blood flow rates in the femora of a variety of extinct and extant avialans are estimated by Hu et al. (2023).[314]
- The visual fields of Hesperornis and extant foot-propelled diving birds are estimated by Pecsics & Csörgő (2023).[315]
- Zelenkov & Arkhangelsky (2023) describe new fossil material of Campanian hesperornithids from the Karyakino locality (Saratov Oblast, Russia), including the first femur of Hesperornis rossicus.[316]
- A synsacrum and a tarsometatarsus assigned to the Vegaviidae from the Upper Cretaceous López de Bertodano Formation (Antarctica) are described by de Souza et al. (2023).[317]
- A study on the anatomy of the articular region of the lower jaw of Vegavis iaai is published by Álvarez-Herrera et al. (2023), who report the presence of anatomical features shared with modern neornithine birds, and particularly with members of the neoavian clade Aequorlitornithes.[318]
- Acosta Hospitaleche, O'Gorman & Panzeri (2023) describe a partial ulna of a bird (comparable in size with ulnae of the coscoroba swan or the southern screamer) from the Maastrichtian La Colonia Formation (Argentina), showing similarities to ulnae of members of Anseriformes and possibly representing the first record of a neornithine from the La Colonia Formation.[319]
- Evidence from the study of eggshell fragments of Diamantornis laini from the Marsawdad Formation (Oman), interpreted as indicating that the deposits containing the eggshells are approximately 8-7 million years old, is presented by Pickford et al. (2023).[320]
- Mourer-Chauviré, Pickford & Senut (2023) describe new fossil material of Struthio coppensi from the Miocene sites in the Sperrgebiet (Namibia).[321]
- Buffetaut (2023) reports the discovery of a plaster cast of the lost femur of Struthio anderssoni from the late Pleistocene deposits of the Upper Cave at Zhoukoudian (China), and transfers the species S. anderssoni to the genus Pachystruthio.[322]
- The body mass and running speed of Opisthodactylus kirchneri are estimated by Jones, Vezzosi & Blanco (2023).[323]
- A study on the evolutionary history of the elephant birds, based on data from fossil eggshells, is published by Grealy et al. (2023), who interpret their findings as supporting the placement of Mullerornis into a separate family, as well as indicative of the existence of a genetically distinct lineage of Aepyornis in Madagascar's far north, report evidence of divergence within Aepyornis corresponding with the onset of the Quaternary, and tentatively advocate synonymising Vorombe titan with Aepyornis maximus.[324]
- Tracks made by moa from the Pliocene–Pleistocene Maniototo Conglomerate Formation (New Zealand) are described by Fleury et al. (2023).[325]
- A study on the formation of the rhamphotheca in the middle-latest Eocene Antarctic pelagornithids is published by Piro & Acosta Hospitaleche (2023).[326]
- A study on the histology of long bones of Lutetodontopteryx tethyensis and cf. Dasornis sp. from the Eocene (Lutetian) locality Ikove (Luhansk Oblast) is published by Dobrovolsky (2023).[327]
- Aspects of the life history of Lutetodontopteryx tethyensis and cf. Dasornis sp. are inferred based on bone histology by Dobrovolsky & Gorobets (2023).[328]
- The impact of including fossil taxa on inferring the ancestral morphology of the quadrate in Galloanserae is studied by Kuo, Benson & Field (2023).[329]
- Revision of small-bodied ducks from the Miocene localities in France and Mongolia is published by Zelenkov (2023), who transfers the species Anas velox to the genus Protomelanitta and transfers the species Anas soporata to the genus Mioquerquedula.[330]
- Fossils of hazel grouse from the Quaternary of Bulgaria are documented by Boev (2023).[331]
- Mayr et al. (2023) describe bird cervical vertebrae from the Quercy fissure fillings (France), densely covered with tubercles similar to those reported in members of the genus Perplexicervix and in "Dynamopterus" tuberculatus from the Messel pit in Germany as well as in extant maned rat, and interpret these tubercles as a feature of distinctive clade of Eocene birds (Perplexicervicidae), possibly representing an anti-predator adaptation against the killing bite of mammalian carnivores.[332]
- An egg belonging to a flamingo from the Pleistocene of Mexico is described by Cruz et al. (2023).[333]
- Fossils of small rails from the late Pleistocene and early Holocene of the Southern High Plains are described by Moretti & Johnson (2023).[334]
- The evolutionary history of the takahē and moho are inferred through analyses of ancient mitochondrial genomes by Verry et al. (2023).[335]
- A study of Pleistocene fossils from the Naracoorte Caves (Australia) by Lenser & Worthy (2023) confirmed the presence of plains-wanderer in the fossil assemblages at this site, and suggests that this species formerly inhabited forest and woodland environments.[336]
- Fossils of the red-throated loon and an undetermined species of Gavia are described from the Pleistocene Liuchungchi Formation (Taiwan) by Wu et al. (2023), representing the first Pleistocene records of Gaviidae in the subtropical Northwest Pacific reported to date.[337]
- Ecomorphology of the penguin wing is studied by Haidr (2023), finding that Madrynornis resembled extant piscivorous penguins in its wing morphology.[338]
- A skull of a small penguin, possibly representing a new species belonging to the genus Spheniscus, Eudyptula or to a new genus ancestral to both listed genera, is described from the Miocene Bahía Inglesa Formation (Chile) by Acosta Hospitaleche & Soto-Acuña (2023).[339]
- Figueiredo et al. (2023) report a partial coracoid of the genus Morus from the middle Miocene (Langhian) of the Setúbal Peninsula (Portugal), an instance that represents the first Miocene sulid described from the Iberian Peninsula.[340]
- Ksepka & Tennyson (2023) report the discovery of the humerus of a probable stem gannet from the Hurupi Formation, representing the oldest record of a sulid from New Zealand reported to date.[341]
- Guilherme et al. (2023) describe fossil material of Macranhinga sp. and Anhinga minuta from the Acre conglomerate member in the southwestern Amazon region, suggesting the presence of potentially three distinct darter taxa within the same locality during the late Miocene.[342]
- Osteological comparisons and historical accounts of recently extinct island night herons are presented by Hume (2023).[343]
- The relationship between skull morphology and feeding ecology of vultures is studied by Steinfield et al. (2023), finding that Breagyps may have belonged to the "gulper" feeding guild, which specializes in feeding on the soft internal tissues of carcasses.[344]
- Coprolites of bearded vultures from the Pleistocene of Portugal are described by Sanz et al. (2023).[345]
- A tarsometatarsus of a cinereous vulture from the Late Pleistocene Gansuiji Formation (Japan) is described by Matsuoka & Hasegawa (2023), representing the first fossil record of this species from Japan.[346]
- Pellets and a fragmentary beak of a barn owl from the Holocene of Socotra Island (Yemen) are reported by Ramello et al. (2023).[347]
- The first known phorusrhacid footprints are described from the Río Negro Formation (Argentina) by Melchor et al. (2023), who name a new ichnotaxon Rionegrina pozosaladensis, and interpret the studied footprints as indicative of a primary role of digit III, secondary role of digit IV and a reduced role of digit II in body weight support.[348]
- Changes in the diversity of amazon parrots in the Caribbean are inferred through analyses of genetic sequences from ancient and modern specimens by Oswald et al. (2023).[349]
- Stidham, O'Connor & Li (2023) reexamine the holotype of Corvus fangshannus and reinterpret it as a member of the sedentary Northern Raven (Corvus corax) lineage.[350]
- Baumann et al. (2023) report isotopic data from raven remains from early Gravettian sites in Southern Moravia (Czech Republic), interpreted as indicating that the studied ravens consumed the same range of foods as contemporaneous Gravettian foragers, regularly feeding on larger herbivores and especially mammoths.[351]
- A review and update of the Cenozoic fossil record of birds in Argentina is published by Tambussi, Degrange & de Mendoza (2023).[352]
- Mourer-Chauviré et al. (2023) describe fossil material of a songbird of uncertain affinities, a lovebird of uncertain specific assignment and cf. Palaeortyx from the Miocene deposits at Grillental (Namibia), representing some of the earliest records of their respective groups in Africa reported to date.[353]
- Changes in body size of birds from the Yucatán peninsula since the Late Pleistocene are documented by Silva-Martínez et al. (2023).[354]
- Fossil material of birds from the Pleistocene of La Crouzade Cave (France) is described by Garcia-Fermet et al. (2023).[355]
- Neto de Carvalho et al. (2023) describe an assemblage of bird trace fossils from a Pleistocene coastal aeolianite unit from the south-west Portugal, including two new forms of traces: Corvidichnus odemirensis, likely produced by the western jackdaw, and Buboichnus vicentinus, attributed to the locomotion and feeding behaviour of a large eagle-owl.[356]
- Gala, Laroulandie & Lenoble (2024) revise the record of bird remains from the Guadeloupe Islands spanning the last 30,000 years, providing evidence of direct and indirect human impact on changes of local bird communities.[357]
Pterosaurs
[edit]New pterosaur taxa
[edit]Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images | |
---|---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
In press |
Martill et al. |
Late Jurassic (late Kimmeridgian to Tithonian) |
A member of the family Ctenochasmatidae. The type species is B. maeuseri. |
|||||
Cratonopterus[359] |
Gen. et sp. nov |
Valid |
Jiang et al. |
Early Cretaceous |
A member of the family Ctenochasmatidae. The type species is C. huabei. |
||||
Eopteranodon yixianensis[360] |
Sp. nov |
Zhang et al. |
Early Cretaceous |
A member of the family Tapejaridae. |
|||||
Gen. et comb. nov |
Valid |
Pêgas et al. |
Early Cretaceous |
A member of the family Tapejaridae. The type species is "Huaxiapterus" corollatus Lü et al. (2006). |
|||||
Gen. et sp. nov |
Valid |
Fernandes et al. |
Late Jurassic (Kimmeridgian-Tithonian) |
A member of the family Ctenochasmatidae belonging to the subfamily Gnathosaurinae. The type species is L. almadrava. |
|||||
Gen. et sp. et comb. nov |
Valid |
Wang et al. |
Early Cretaceous (Barremian-Aptian) |
Jiufotang Formation |
A member of the family Chaoyangopteridae. The type species is M. youhao; genus also includes "Shenzhoupterus" sanyainus Ji, Zhang & Lu (2023). |
||||
Gen. et sp. nov |
Valid |
Hone et al. |
Late Jurassic |
A member of the family Gallodactylidae. The type species is P. wellnhoferi. |
|||||
Sp. nov |
In press |
Ji et al. |
Early Cretaceous |
A member of the family Chaoyangopteridae. Originally described as a species of Shenzhoupterus; Wang et al. (2023) transferred it to the genus Meilifeilong.[363] |
Pterosaur research
[edit]- A study on the diversification of pterosaurs during their evolutionary history, aiming to determine the factors that affected pterosaur evolution, is published by Yu, Zhang & Xu (2023).[366]
- A study comparing the sternal anatomy of 60 different pterosaur species is published by Hone (2023).[367]
- Yang et al. (2023) compare wing ontogeny and performance in Rhamphorhynchus, Pterodactylus, Sinopterus and Pteranodon, and interpret the differences in the growth patterns of the studied pterosaurs as suggestive of more altricial development in Pteranodon than in smaller-bodied pterosaurs.[368]
- Review of the fossil record of Jurassic and Cretaceous pterosaurs from Gondwana is published by Pentland & Poropat (2023).[369]
- Revision of the pterosaur assemblage from the Kem Kem Group (Morocco) is published by Smith et al. (2023), who provide revised diagnoses for Afrotapejara zouhrii and Alanqa saharica, and report at least three distinct jaw morphotypes which cannot be referred to any previously named species.[370]
- Jagielska et al. (2023) describe a non-pterodactyloid pterosaur specimen from the Bathonian Lealt Shale (Isle of Skye, Scotland, United Kingdom), preserving metatarsal and caudal vertebrae which are considerably larger than corresponding bones in the holotype of Dearc sgiathanach.[371]
- A study on the surface of the holotype specimen of Scaphognathus crassirostris, providing evidence of the presence of six different types of pycnofibers, is published by Henkemeier, Jäger & Sander (2023).[372]
- The oldest pterosaur remains found in Australia to date, including the first fossil material of a juvenile pterosaur from Australia, is described from the Lower Cretaceous Eumeralla Formation by Pentland et al. (2023).[373]
- A study on the microstructure of the tooth and periodontium attachment tissues of Pterodaustro guinazui is published by Cerda & Codorniú (2023), who report that teeth of this pterosaur were set in a groove with no interdental separation, and find no evidence for gomphosis or the presence of replacement teeth.[374]
- Pterosaur teeth which might represent the earliest record of Istiodactylidae reported to date are described from the Valanginian Wadhurst Clay Formation (United Kingdom) by Sweetman (2023).[375]
- The geologically oldest specimen of Nurhachius reported to date is described from the Lower Cretaceous Jingangshan Member of the Yixian Formation (China) by Ozeki et al. (2023).[376]
- Description of the pectoral girdle morphology and histology in Hamipterus, providing evidence of both the similarities and differences between the flight apparatus of pterosaurs and birds, is published by Wu et al. (2023).[377]
- A study on the microstructure of teeth of Hamipterus, providing evidence of thin enamel that covered approximately half of the tooth crown, is published by Chen et al. (2023).[378]
- Richards, Stumkat & Salisbury (2023) describe a new specimen of the Thapunngaka from the Lower Cretaceous (Albian) Toolebuc Formation (Australia), consisting of parts of the premaxillary and maxillary rostrum, and two new clades of tropeognathines, Mythungini and Tropeognathini.[379]
- Smith, Martill & Zouhri (2023) reinterpret a purported shark spine from the Cenomanian Cambridge Greensand Member of the West Melbury Marly Chalk Formation (Cambridgeshire, United Kingdom) as a jaw fragment of an azhdarchoid distinct from Ornithostoma sedgwicki, but sharing a distinctive morphology with jaw fragments reported from the Kem Kem Beds of Morocco.[380]
- Song, Jiang & Wang (2023) redescribe purported dsungaripterid remains from the Lower Cretaceous (Albian) Doushan Formation (China), assign the most complete element (a femur) to Azhdarchoidea, and study osteological correlates for thigh muscles on the femur, interpreting their general pattern as conservative when compared with other basal ornithodirans.[381]
- New Jehol tapejarid skeleton, probably belonging to a specimen of Sinopterus dongi and providing new information on the skull anatomy in this species, is described by Zhou, Miao & Andres (2023).[382]
- A study on the affinities of "Tupuxuara" deliradamus is published by Cerqueira, Müller & Pinheiro (2023), who interpret this pterosaur as a tapejarine.[383]
- A study on the ontogeny of Caiuajara dobruskii, as inferred from its bone histology, is published by de Araújo et al. (2023).[384]
- Fragmentary wing phalanges from the Aptian-Albian Antlers Formation (Texas, United States), originally noted by Bennett (2001) to be similar in their oval cross-sections to those of Dsungaripterus,[385] are interpreted by Bennett (2023) as possible thalassodromine fossil material.[386]
- Agnolín et al. (2023) report the discovery of a pterosaur cervical vertebra from the Cenomanian Candeleros Formation (Argentina), interpreted as the oldest record of an azhdarchid from South America reported to date.[387]
- Four teeth representing the first pterosaur material from Ukraine reported to date are described from the Lower Cretaceous Burim Formation by Sokolskyi (2023).[388]
Other archosaurs
[edit]Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Müller & Garcia |
Late Triassic (Carnian) |
Candelária Sequence of the Santa Maria Supersequence |
A member of the family Silesauridae. The type species is A. nesbitti. |
||||
Mambachiton[390] | Gen. et sp. nov | Nesbitt et al. | Late Triassic | Isalo II | Madagascar | A basal member of Avemetatarsalia. The type species is M. fiandohana. | ||
Gen. et sp. nov |
Valid |
Müller et al. |
Late Triassic |
Candelária Sequence of the Santa Maria Supersequence |
A member of the family Lagerpetidae. The type species is V. gassenae. |
Other archosaur research
[edit]- Redescription of the skeletal anatomy of Scleromochlus taylori is published by Foffa et al. (2023), who interpret S. taylori as a lagerpetid.[392]
- Description of the anatomy of the braincase of Dromomeron gregorii is published by Bronzati et al. (2023), who also present reconstructions of soft tissues associated with the braincase, and report that sensory structures of D. gregorii were more similar to those of pterosaurs than to those of other early avemetatarsalians.[393]
- Mestriner et al. (2023) describe an assemblage of silesaurid remains from the Waldsanga locality from the Santa Maria Formation (Brazil), providing evidence of the presence of a combination of dinosauromorph symplesiomorphies and silesaurid diagnostic traits in the postcranial skeletons of the studied specimens.[394]
General research
[edit]- Wang, Claessens & Sullivan (2023) establish skeletal features associated with the attachment of uncinate processes to vertebral ribs in extant birds and crocodilians, attempt to determine their distribution in fossil archosaurs, and interpret their findings as indicating that cartilaginous uncinate processes were plesiomorphically present (and likely had a ventilatory function) in dinosaurs, and maybe even in archosaurs in general.[395]
- Aureliano et al. (2023) present the criteria which can be used to distinguish between lamellar bone fibres, Sharpey's fibres (tendon insertions) and air sac attachments in the bones of fossil archosaurs.[396]
- De-Oliveira et al. (2023) report the discovery of an isolated tooth from the São Luiz Site (Candelária Sequence; Brazil), providing evidence of the presence of a previously unknown medium or large-sized carnivorous archosaur at the site.[397]
- Abrahams & Bordy (2023) reevaluate tracks assigned to the ichnogenus Trisauropodiscus from the Upper Triassic–Lower Jurassic Elliot Formation, and report that the studied material includes tracks produced by a yet-unknown tridactyl archosaur with a bird-like foot morphology.[398]
- Figueiredo et al. (2023) describe crocodylomorph and thyreophoran dinosaur tracks from the Lower Jurassic (Sinemurian) Coimbra Formation (Portugal), and name a new ichnotaxon Moyenisauropus lusitanicus.[399]
- A possible didactyl deinonychosaurian track and an assemblage of pterosaur tracks is reported from the Jurassic Santai Formation (Shandong, China) by Xing et al. (2023).[400]
- Evidence indicative of Valanginian maximum age for the Urho Pterosaur Fauna from the Tugulu Group in Junggar Basin (Xinjiang, China) is presented by Zheng et al. (2023).[401]
- Juarez et al. (2023) corroborate the identification of abelisaurid and peirosaurid teeth from the Upper Cretaceous Ciénaga del Río Huaco Formation, representing the first record of both groups from the Upper Cretaceous of the Precordillera of La Rioja (Argentina).[402]
- Putative avialan teeth from the Late Cretaceous of Alberta, Canada are reinterpreted as belonging to crocodylians by Mohr, Acorn & Currie (2023).[403]
- Taphonomic effects of fossilization on melanin in feathers are experimentally investigated by Roy et al. (2023).[404]
- Evidence from taphonomic experiments, interpreted as indicating that putative keratins reported from fossil feathers are most likely artefacts of fossilization, but also indicating that corneous β-proteins of feathers can persist through deep time, is presented by Slater et al. (2023).[405]
- A review of the evolution of nest site use and nest architecture in avian and non-avian dinosaurs is published by Mainwaring et al. (2023).[406]
- Evidence of changes in eggshell structure throughout embryonic development of the broad-snouted caiman is presented by Fernández, Piazza & Simoncini (2023), who interpret their findings as potentially explaining the differences in porosity and thickness of dinosaur eggshells found at different levels in fossil deposits with broods.[407]
References
[edit]- ^ Darlim, G.; Suraprasit, K.; Chaimanee, Y.; Tian, P.; Yamee, C.; Rugbumrung, M.; Kaweera, A.; Rabi, M. (2023). "An extinct deep-snouted Alligator species from the Quaternary of Thailand and comments on the evolution of crushing dentition in alligatorids". Scientific Reports. 13 (1). 10406. Bibcode:2023NatSR..1310406D. doi:10.1038/s41598-023-36559-6. PMC 10344928. PMID 37443318.
- ^ Martin, J. E.; Naksri, W.; Lauprasert, K.; Wongko, K.; Chompusri, S.; Sila, S.; Claude, J. (2023). "An early diverging crocodylid from the Middle Miocene of Thailand highlights the role of SE Asia for the radiation of the Crocodyloidea". Historical Biology: 1–10. doi:10.1080/08912963.2023.2278152. S2CID 265188490.
- ^ Martins, K. C.; Queiroz, M. V.; Ruiz, J. V.; Langer, M. C.; Montefeltro, F. C. (2023). "A new Baurusuchidae (Notosuchia, Crocodyliformes) from the Adamantina Formation (Bauru Group, Upper Cretaceous), with a revised phylogenetic analysis of Baurusuchia". Cretaceous Research. 153. 105680. doi:10.1016/j.cretres.2023.105680. S2CID 261182849.
- ^ Yates, Adam M.; Ristevski, Jorgo; Salisbury, Steven W. (2023). "The last Baru (Crocodylia, Mekosuchinae): a new species of 'cleaver-headed crocodile' from central Australia and the turnover of crocodylians during the Late Miocene in Australia". Papers in Palaeontology. 9 (5). Bibcode:2023PPal....9E1523Y. doi:10.1002/spp2.1523. ISSN 2056-2799. S2CID 262592438.
- ^ Kellner, A. W. A.; Figueiredo, R. G.; Calvo, J. O. (2023). "A new species of Comahuesuchus Bonaparte, 1991 (Crocodyliformes: Notosuchia) from the Upper Cretaceous of Neuquén, Lake Barreales, Patagonia, Argentina". Anais da Academia Brasileira de Ciências. 95 (Suppl. 1). e20230179. doi:10.1590/0001-3765202320230179. PMID 37585972. S2CID 260910113.
- ^ Martin, J. E.; Pochat-Cottilloux, Y.; Laurent, Y.; Perrier, V.; Robert, E.; Antoine, P.-O. (2023). "Anatomy and phylogeny of an exceptionally large sebecid (Crocodylomorpha) from the middle Eocene of southern France". Journal of Vertebrate Paleontology. 42 (4). e2193828. doi:10.1080/02724634.2023.2193828. S2CID 258361595.
- ^ Kischlat, Edio-Ernst (2023). "A new nominal genus for "Prestosuchus" chiniquensis Huene, 1938 (Triassic of southern Brazil): Huenesuchus, genus novus et combinatio nova". Revista Brasileira de Paleontologia. 26 (2): 69–96. doi:10.4072/rbp.2023.2.01. S2CID 259941612.
- ^ Reyes, William A.; Parker, William G.; Heckert, Andrew B. (2023). "A new aetosaur (Archosauria: Pseudosuchia) from the upper Blue Mesa Member (Adamanian: Early–Mid Norian) of the Late Triassic Chinle Formation, northern Arizona, USA, and a review of the paratypothoracin Tecovasuchus across the southwestern USA". PaleoBios. 40 (9). doi:10.5070/P940961559. ISSN 0031-0298. S2CID 259972056.
- ^ a b Sennikov, A. G. (2022). "A New Pseudosuchian from the Early Triassic of Eastern Europe". Paleontological Journal. 56 (11): 1391–1418. Bibcode:2022PalJ...56.1391S. doi:10.1134/S0031030122110168. S2CID 256618821.
- ^ Girard, L. C.; De Sousa Oliveira, S.; Raselli, I.; Martin, J. E.; Anquetin, J. (2023). "Description and phylogenetic relationships of a new species of Torvoneustes (Crocodylomorpha, Thalattosuchia) from the Kimmeridgian of Switzerland". PeerJ. 11. e15512. doi:10.7717/peerj.15512. PMC 10362849. PMID 37483966.
- ^ Wilberg, E. W.; Godoy, P. L.; Griffiths, E. F.; Turner, A. H.; Benson, R. B. J. (2023). "A new early diverging thalattosuchian (Crocodylomorpha) from the Early Jurassic (Pliensbachian) of Dorset, U.K. and implications for the origin and evolution of the group". Journal of Vertebrate Paleontology. 42 (3). e2161909. doi:10.1080/02724634.2022.2161909. S2CID 256149424.
- ^ Haldar, A.; Ray, S.; Bandyopadhyay, S. (2023). "A new typothoracine aetosaur (Archosauria, Pseudosuchia) from the Upper Triassic of India with insights on biostratigraphy, diversification, and paleobiogeography". Journal of Vertebrate Paleontology. 43 (1). e2253292. doi:10.1080/02724634.2023.2253292. S2CID 265506966.
- ^ Payne, A. R. D.; Mannion, P. D.; Lloyd, G. T.; Davis, K. E. (2023). "Decoupling speciation and extinction reveals both abiotic and biotic drivers shaped 250 million years of diversity in crocodile-line archosaurs". Nature Ecology & Evolution. 8 (1): 121–132. Bibcode:2023NatEE...8..121P. doi:10.1038/s41559-023-02244-0. PMC 10781641. PMID 38049481.
- ^ Taborda, J. R. A.; Von Baczko, M. B.; Desojo, J. B. (2023). "Biomechanical analysis and new trophic hypothesis for Riojasuchus tenuisceps, a bizarre-snouted Late Triassic pseudosuchian from Argentina". Acta Palaeontologica Polonica. 68 (3): 415–425. doi:10.4202/app.01038.2022. hdl:11336/226208. S2CID 261551160.
- ^ Farias, B. D. M.; Desojo, J. B.; Cerda, I. A.; Ribeiro, A. M.; Ferigolo, J.; Carlisbino, T.; Schultz, C. L.; Mastrantonio, B. M.; Soares, M. B. (2023). "Bone histology supports gregarious behavior and an early ontogenetic stage to Decuriasuchus quartacolonia (Pseudosuchia: Loricata) from the Middle-Late Triassic of Brazil". The Anatomical Record. 307 (4): 957–973. doi:10.1002/ar.25365. PMID 38088505. S2CID 266228833.
- ^ Ponce, D. A.; Scheyer, T. M.; Cerda, I. A.; Desojo, J. B. (2023). "Palaeobiological inferences of "rauisuchians" Fasolasuchus tenax (Los Colorados Fm., Argentina) and Prestosuchus chiniquensis (Santa Maria Super sequence, Brazil) from the Middle–Upper Triassic of South America based on microstructural analyses". Journal of Anatomy. 243 (6): 893–909. doi:10.1111/joa.13937. PMC 10641045. PMID 37519277. S2CID 260332648.
- ^ Fawcett, M. J.; Lautenschlager, S.; Bestwick, J.; Butler, R. J. (2023). "Functional morphology of the Triassic apex predator Saurosuchus galilei (Pseudosuchia: Loricata) and convergence with a post-Triassic theropod dinosaur". The Anatomical Record. 307 (3): 549–565. doi:10.1002/ar.25299. PMID 37584310. S2CID 260924469.
- ^ von Baczko, M. B.; Cardillo, A. F.; Ulloa-Guaiquin, K.; Desojo, J. B.; Paulina-Carabajal, A. (2023). "Paleoneurology and neuroanatomical notes on the South American "rauisuchian" Saurosuchus galilei from the Ischigualasto formation, San Juan, Argentina". The Anatomical Record. 307 (4): 1239–1253. doi:10.1002/ar.25362. PMID 38133536. S2CID 266467568.
- ^ Tolchard, F. B.; Bordy, E. M.; Choiniere, J. N. (2023). "New 'rauisuchian' fossil material from the lower Elliot Formation of South Africa". Palaeontologia Africana. 56: 180–189. hdl:10539/37138.
- ^ Lehane, J. R. (2023). "Cranial anatomy of Shuvosaurus inexpectatus, an edentulous poposauroid pseudosuchian from the Late Triassic of Texas". Historical Biology: 1–26. doi:10.1080/08912963.2023.2241056. S2CID 260463644.
- ^ Teschner, E. M.; Konietzko-Meier, D.; Desojo, J. B.; Schoch, R. R.; Klein, N. (2023). "Triassic Nursery? Evidence of gregarious behavior in juvenile pseudosuchian archosaurs as inferred by humeral histology of Aetosaurus ferratus (Norian; southern Germany)". Journal of Vertebrate Paleontology. 42 (2). e2168196. doi:10.1080/02724634.2023.2168196. S2CID 256864004.
- ^ Parker, W. G.; Reyes, W. A.; Marsh, A. D. (2023). "Incongruent ontogenetic maturity indicators in a Late Triassic archosaur (Aetosauria: Typothorax coccinarum)". The Anatomical Record. 307 (4): 1254–1270. doi:10.1002/ar.25343. PMID 37937738. S2CID 265049520.
- ^ Botha, J.; Weiss, B. M.; Dollman, K.; Barrett, P. M.; Benson, R. B. J.; Choiniere, J. N. (2023). "Origins of slow growth on the crocodilian stem lineage". Current Biology. 33 (19): 4261–4268.e3. Bibcode:2023CBio...33E4261B. doi:10.1016/j.cub.2023.08.057. PMID 37714148. S2CID 261753190.
- ^ Spiekman, S. N. F. (2023). "A revision and histological investigation of Saltoposuchus connectens (Archosauria: Crocodylomorpha) from the Norian (Late Triassic) of south-western Germany". Zoological Journal of the Linnean Society. 199 (2): 354–391. doi:10.1093/zoolinnean/zlad035.
- ^ Spiekman, S. N. F.; Fernandez, V.; Butler, R. J.; Dollman, K. N.; Maidment, S. C. R. (2023). "A taxonomic revision and cranial description of Terrestrisuchus gracilis (Archosauria, Crocodylomorpha) from the Upper Triassic of Pant-y-Ffynnon Quarry (southern Wales)". Papers in Palaeontology. 9 (6). e1534. Bibcode:2023PPal....9E1534S. doi:10.1002/spp2.1534.
- ^ Lessner, E. J.; Dollman, K. N.; Clark, J. M.; Xu, X.; Holliday, C. M. (2023). "Ecomorphological patterns in trigeminal canal branching among sauropsids reveal sensory shift in suchians". Journal of Anatomy. 242 (5): 927–952. doi:10.1111/joa.13826. PMC 10093182. PMID 36680380. S2CID 256055306.
- ^ de Araújo Sena, M. V.; Cubo, J. (2023). "Inferring the lifestyles of extinct Crocodyliformes using osteoderm ornamentation". The Science of Nature. 110 (5). 41. Bibcode:2023SciNa.110...41D. doi:10.1007/s00114-023-01871-8. PMID 37548714. S2CID 260621242.
- ^ Young, M. T.; Bowman, C. I. W.; Erb, A.; Schwab, J. A.; Witmer, L. M.; Herrera, Y.; Brusatte, S. L. (2023). "Evidence for a novel cranial thermoregulatory pathway in thalattosuchian crocodylomorphs". PeerJ. 11. e15353. doi:10.7717/peerj.15353. PMC 10162039. PMID 37151298.
- ^ Johnson, M. M.; Amson, E.; Maxwell, E. E. (2023). "Evaluating growth in Macrospondylus bollensis (Crocodylomorpha, Teleosauroidea) in the Toarcian Posidonia Shale, Germany". Papers in Palaeontology. 9 (5). e1529. Bibcode:2023PPal....9E1529J. doi:10.1002/spp2.1529.
- ^ Young, M. T.; Zverkov, N. G.; Arkhangelsky, M. S.; Ippolitov, A. P.; Meleshin, I. A.; Mirantsev, G. V.; Shmakov, A. S.; Stenshin, I. M. (2023). "Thalattosuchian crocodylomorphs from European Russia, and new insights into metriorhynchid tooth serration evolution and their palaeolatitudinal distribution". PeerJ. 11. e15781. doi:10.7717/peerj.15781. PMC 10424675. PMID 37583913.
- ^ Serafini, G.; Foffa, D.; Young, M. T.; Friso, G.; Cobianchi, M.; Giusberti, L. (2023). "Reappraisal of the thalattosuchian crocodylomorph record from the Middle-Upper Jurassic Rosso Ammonitico Veronese of northeastern Italy: Age calibration, new specimens and taphonomic biases". PLOS ONE. 18 (10). e0293614. Bibcode:2023PLoSO..1893614S. doi:10.1371/journal.pone.0293614. PMC 10615311. PMID 37903146.
- ^ Scavezzoni, I.; Fischer, V. (2023). "Limited convergence in the postcranium of aquatic Crocodylomorpha". Palaeontology. 66 (6). e12678. Bibcode:2023Palgy..6612678S. doi:10.1111/pala.12678. hdl:2268/305703. S2CID 265202788.
- ^ Wu, L.; Wu, X.-C.; You, H.-L.; Zhang, Y.; Zhao, J.; Yuan, Y.; Zhang, H.; Li, S. (2023). "A new specimen of Hsisosuchus (Mesoeucrocodylia, Crocodyliformes) from the Upper Jurassic of Yunnan, China with implications for the diversity of the ventral trunk shield of osteoderms in the genus". Historical Biology. 36 (3): 550–561. doi:10.1080/08912963.2023.2170796. S2CID 256564315.
- ^ de Araújo Sena, M. V.; Montefeltro, F. C.; Marinho, T. S.; Langer, M. C.; Fachini, T. S.; Pinheiro, A. E. P.; Machado, A. S.; Lopes, R. T.; Pellarin, R.; Sayão, J. M.; Oliveira, G. R.; Cubo, J. (2023). "The cost of living in Notosuchia (Crocodyliformes, Mesoeucrocodylia)". Palaeogeography, Palaeoclimatology, Palaeoecology. 632. 111855. Bibcode:2023PPP...63211855S. doi:10.1016/j.palaeo.2023.111855. S2CID 264149406.
- ^ Aubier, P.; Jouve, S.; Schnyder, J.; Cubo, J. (2023). "Phylogenetic structure of the extinction and biotic factors explaining differential survival of terrestrial notosuchians at the Cretaceous–Palaeogene crisis". Palaeontology. 66 (1). e12638. Bibcode:2023Palgy..6612638A. doi:10.1111/pala.12638. S2CID 257137911.
- ^ Faure-Brac, M. G.; Cubo, J. (2023). "Is there any evidence for the presence of extensive fibrolamellar complex in Notosuchia? New data on Araripesuchus wegeneri". Lethaia. 56 (3): 1–6. Bibcode:2023Letha..56..3.2F. doi:10.18261/let.56.3.2. S2CID 261762510.
- ^ Navarro, T. G.; Cerda, I. A.; Pol, D. (2023). "Microstructural characterization and growth dynamics in Notosuchus terrestris, a Mesoeucrocodylia crocodyliform from the Upper Cretaceous of Northern Patagonia, Argentina". Cretaceous Research. 150. 105607. Bibcode:2023CrRes.15005607N. doi:10.1016/j.cretres.2023.105607. S2CID 259797088.
- ^ Andrade, R. C. L. P.; Sena, M. V. A.; Brum, A. S.; Campos, D. A.; Kellner, A. W. A.; Bantim, R. A. M. B.; Sayão, J. M. (2023). "Osteohistology of the big-sized Cretaceous crocodylomorph Stratiotosuchus maxhechti (Notosuchia, Baurusuchidae) indicates fast growth and niche partitioning with medium-sized theropods". Journal of South American Earth Sciences. 104363. doi:10.1016/j.jsames.2023.104363. S2CID 258266695.
- ^ Pinheiro, A. E. P.; Pereira, P. V. L. G. C.; Vasconcellos, F. M.; Brum, A. S.; Souza, L. G.; Costa, F. R.; Castro, L. O. R.; Silva, K. F.; Bandeira, K. L. N. (2023). "New Itasuchidae (Sebecia, Ziphosuchia) remains and the radiation of an elusive Mesoeucrocodylia clade". Historical Biology. 35 (12): 2280–2305. Bibcode:2023HBio...35.2280P. doi:10.1080/08912963.2022.2139179. S2CID 255664924.
- ^ Pochat-Cottilloux, Y.; Perrier, V.; Amiot, R.; Martin, J.E. (2023). "A peirosaurid mandible from the Albian–Cenomanian (Lower Cretaceous) of Algeria and the taxonomic content of Hamadasuchus (Crocodylomorpha, Peirosauridae)". Papers in Palaeontology. 9 (2). Bibcode:2023PPal....9E1485P. doi:10.1002/spp2.1485. S2CID 257842011.
- ^ Pochat-Cottilloux, Y.; Rinder, N.; Perrichon, G.; Adrien, J.; Amiot, R.; Hua, S.; Martin, J. E. (2023). "The neuroanatomy and pneumaticity of Hamadasuchus (Crocodylomorpha, Peirosauridae) from the Cretaceous of Morocco and its paleoecological significance for altirostral forms". Journal of Anatomy. 243 (3): 374–393. doi:10.1111/joa.13887. PMC 10439374. PMID 37309776. S2CID 259148269.
- ^ Pochat-Cottilloux, Y.; Martin, J. E.; Faure-Brac, M. G.; Jouve, S.; de Muizon, C.; Cubo, J.; Lécuyer, C.; Fourel, F.; Amiot, R. (2023). "A multi-isotopic study reveals the palaeoecology of a sebecid from the Paleocene of Bolivia" (PDF). Palaeogeography, Palaeoclimatology, Palaeoecology. 625. 111667. Bibcode:2023PPP...62511667P. doi:10.1016/j.palaeo.2023.111667. S2CID 259787887.
- ^ Groh, S. S.; Upchurch, P.; Day, J. J.; Barrett, P. M. (2023). "The biogeographic history of neosuchian crocodiles and the impact of saltwater tolerance variability". Royal Society Open Science. 10 (10). 230725. Bibcode:2023RSOS...1030725G. doi:10.1098/rsos.230725. PMC 10548099. PMID 37800151.
- ^ Muscioni, M.; Chiarenza, A. A.; Delfino, M.; Fabbri, M.; Milocco, K.; Fanti, F. (2023). "Acynodon adriaticus from Villaggio del Pescatore (Campanian of Italy): anatomical and chronostratigraphic integration improves phylogenetic resolution in Hylaeochampsidae (Eusuchia)". Cretaceous Research. 151. 105631. Bibcode:2023CrRes.15105631M. doi:10.1016/j.cretres.2023.105631. hdl:11093/5418. S2CID 259670508.
- ^ Adams, T. L.; Drumheller, S. K.; Noto, C. R. (2023). "Paleodiversity and niche partitioning of crocodyliforms from the Woodbine Group (Late Cretaceous: Cenomanian)". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 99–119. ISBN 978-89-5708-358-1.
- ^ Ristevski, J.; Willis, P. M. A.; Yates, A. M.; White, M. A.; Hart, L. J.; Stein, M. D.; Price, G. J.; Salisbury, S. W. (2023). "Migrations, diversifications and extinctions: the evolutionary history of crocodyliforms in Australasia". Alcheringa: An Australasian Journal of Palaeontology. 47 (4): 370–415. Bibcode:2023Alch...47..370R. doi:10.1080/03115518.2023.2201319. S2CID 258878554.
- ^ Venczel, M. (2023). "Updating the fossil record of the alligatoroid crocodylian Diplocynodon from the late Eocene of Transylvanian Basin". Frontiers in Amphibian and Reptile Science. 1. 1217025. doi:10.3389/famrs.2023.1217025.
- ^ Bona, P.; Pol, D.; Pérez, L. M.; Tineo, D. E.; Brandoni, D.; Noriega, J. I. (2023). "The first record of Purussaurus (Crocodylia, Alligatoridae) in the Late Miocene of Argentina". Revista del Museo Argentino de Ciencias Naturales. Nueva Series. 25 (1): 71–84. doi:10.22179/REVMACN.25.797. S2CID 260849179.
- ^ Cidade, G. M.; Hsiou, A. S. (2023). "An updated taxonomic revision of the species of Mourasuchus (Alligatoroidea, Caimaninae)". Historical Biology: 1–8. doi:10.1080/08912963.2023.2271506. S2CID 264468427.
- ^ Puértolas-Pascual, E.; Kuzmin, I. T.; Serrano-Martínez, A.; Mateus, O. (2023). "Neuroanatomy of the crocodylomorph Portugalosuchus azenhae from the Late Cretaceous of Portugal". Journal of Anatomy. 242 (6): 1146–1171. doi:10.1111/joa.13836. PMC 10184551. PMID 36732084. S2CID 256546983.
- ^ Venczel, M.; Codrea, M.; Trif, N. (2023). "Eocene gavialoid teeth from southern Transylvania with notes on the diversity of Paleogene crocodilians from Romania" (PDF). North-Western Journal of Zoology. 19 (1).
- ^ Burke, P. M. J.; Mannion, P. D. (2023). "Neuroanatomy of the crocodylian Tomistoma dowsoni from the Miocene of North Africa provides insights into the evolutionary history of gavialoids". Journal of Anatomy. 243 (1): 1–22. doi:10.1111/joa.13846. PMC 10273334. PMID 36929596. S2CID 257581488.
- ^ Cho, Y.-Y.; Tsai, C.-H. (2023). "Crocodylian princess in Taiwan: Revising the taxonomic status of Tomistoma taiwanicus from the Pleistocene of Taiwan and its paleobiogeographic implications". Journal of Paleontology. 97 (4): 927–940. Bibcode:2023JPal...97..927C. doi:10.1017/jpa.2023.36. S2CID 259748336.
- ^ Perrichon, G.; Pochat-Cottilloux, Y.; Conedera, D.; Richardin, P.; Fernandez, V.; Hautier, L.; Martin, J. E. (2023). "Neuroanatomy and pneumaticity of the extinct Malagasy "horned" crocodile Voay robustus and its implications for crocodylid phylogeny and palaeoecology". The Anatomical Record. 307 (8): 2749–2786. doi:10.1002/ar.25367. PMID 38116895.
- ^ a b Lacerda, M.B.S.; de Andrade, M.B.; Sales, M.A.F.; Aragão, P.R.L.; Vieira, F.S.; Bittencourt, J.S.; Liparini, A. (2023). "The vertebrate fossil record from the Feliz Deserto Formation (Lower Cretaceous), Sergipe, NE Brazil: paleoecological, taphonomic, and paleobiogeographic implications". Cretaceous Research. 147: 105463. Bibcode:2023CrRes.14705463L. doi:10.1016/j.cretres.2022.105463. ISSN 0195-6671. S2CID 255635144.
- ^ Halaçlar, Kazım; Rummy, Paul; Liu, Jia; Hunt, Adrian P.; Van Do, Truong; Minh, Nguyen Trung; Deng, Tao (2023-09-15). "Exceptionally well-preserved crocodilian coprolites from the Late Eocene of Northern Vietnam: Ichnology and paleoecological significance". iScience. 26 (9): 107607. Bibcode:2023iSci...26j7607H. doi:10.1016/j.isci.2023.107607. ISSN 2589-0042. PMC 10470398. PMID 37664591.
- ^ Tykoski, Ronald S.; Contreras, Dori L.; Noto, Christopher (2023-10-13). "The first small-bodied ornithopod dinosaur from the Lewisville Formation (middle Cenomanian) of Texas". Journal of Vertebrate Paleontology. 43 (2). e2257238. doi:10.1080/02724634.2023.2257238. ISSN 0272-4634.
- ^ Simón, M. E.; Salgado, L. (2023). "A new gigantic titanosaurian sauropod from the early Late Cretaceous of Patagonia (Neuquén Province, Argentina)". Acta Palaeontologica Polonica. 68 (4): 719–735. doi:10.4202/app.01086.2023.
- ^ Prieto-Márquez, A.; Sellés, A. (2023). "Evolutionary convergence in a small cursorial styracosternan ornithopod dinosaur from western Europe". Journal of Vertebrate Paleontology. 42 (5). e2210632. doi:10.1080/02724634.2023.2210632. S2CID 259335419.
- ^ Agnolin, Federico L.; Gonzalez Riga, Bernardo J.; Aranciaga Rolando, Alexis M.; Rozadilla, Sebastián; Motta, Matías J.; Chimento, Nicolás R.; Novas, Fernando E. (2023-02-02). "A new gigant titanosaur (Dinosauria, Sauropoda) from the Upper Cretaceous of Northwestern Patagonia, Argentina". Cretaceous Research. 146: 105487. Bibcode:2023CrRes.14605487A. doi:10.1016/j.cretres.2023.105487. ISSN 0195-6671. S2CID 256559829.
- ^ Ishikawa, H.; Tsuihiji, T.; Manabe, M. (2023). "Furcatoceratops elucidans, a new centrosaurine (Ornithischia: Ceratopsidae) from the upper Campanian Judith River Formation, Montana, USA". Cretaceous Research. 151. 105660. Bibcode:2023CrRes.15105660I. doi:10.1016/j.cretres.2023.105660. S2CID 260046917.
- ^ Mocho, P.; Escaso, F.; Gasulla, J. M.; Galobart, À.; Poza, B.; Santos-Cubedo, A.; Sanz, J. L.; Ortega, F. (2023). "New sauropod dinosaur from the Lower Cretaceous of Morella (Spain) provides new insights on the evolutionary history of Iberian somphospondylan titanosauriforms". Zoological Journal of the Linnean Society. 201: 214–268. doi:10.1093/zoolinnean/zlad124.
- ^ Alarcón-Muñoz, J.; Vargas, A. O.; Püschel, H. P.; Soto-Acuña, S.; Manríquez, L.; Leppe, M.; Kaluza, J.; Milla, V.; Gutstein, C. S.; Palma-Liberona, J.; Stinnesbeck, W.; Frey, E.; Pino, J. P.; Bajor, D.; Núñez, E.; Ortiz, H.; Rubilar-Rogers, D.; Cruzado-Caballero, P. (2023). "Relict duck-billed dinosaurs survived into the last age of the dinosaurs in subantarctic Chile". Science Advances. 9 (24). eadg2456. Bibcode:2023SciA....9G2456A. doi:10.1126/sciadv.adg2456. PMC 10275600. PMID 37327335.
- ^ Ryan, M.J.; Micucci, L.; Rizo, H.; Sullivan, C.; Lee, Y.-N.; Evans, D.C. (2023). "New Late Cretaceous leptoceratopsid (Dinosauria: Ceratopsia) from the Oldman Formation (Campanian) of Alberta, Canada". In Lee, Y.-N. (ed.). Windows into Sauropsid and Synapsid Evolution: Essays in Honor of Prof. Louis L. Jacobs. Seoul: Dinosaur Science Center Press. pp. 151–165. ISBN 978-89-5708-358-1.
- ^ Zanno, L. E.; Gates, T. A.; Avrahami, H. M.; Tucker, R. T.; Makovicky, P. J. (2023). "An early-diverging iguanodontian (Dinosauria: Rhabdodontomorpha) from the Late Cretaceous of North America". PLOS ONE. 18 (6). e0286042. Bibcode:2023PLoSO..1886042Z. doi:10.1371/journal.pone.0286042. PMC 10246810. PMID 37285376.
- ^ Gorscak, E.; Lamanna, M. C.; Schwarz, D.; Díez Díaz, V.; Salem, B. S.; Sallam, H. M.; Wiechmann, M. F. (2023). "A new titanosaurian (Dinosauria: Sauropoda) from the Upper Cretaceous (Campanian) Quseir Formation of the Kharga Oasis, Egypt". Journal of Vertebrate Paleontology. 42 (6). e2199810. doi:10.1080/02724634.2023.2199810. S2CID 260046761.
- ^ Filippi, Leonardo S.; Juárez Valieri, Rubén D.; Gallina, Pablo A.; Méndez, Ariel H.; Gianechini, Federico A.; Garrido, Alberto C. (2023). "A rebbachisaurid-mimicking titanosaur and evidence of a Late Cretaceous faunal disturbance event in South-West Gondwana". Cretaceous Research. 154. doi:10.1016/j.cretres.2023.105754. ISSN 0195-6671. S2CID 264792693.
- ^ Kubo, K.; Kobayashi, Y.; Chinzorig, T.; Tsogtbaatar, K. (2023). "A new alvarezsaurid dinosaur (Theropoda, Alvarezsauria) from the Upper Cretaceous Baruungoyot Formation of Mongolia provides insights for bird-like sleeping behavior in non-avian dinosaurs". PLOS ONE. 18 (11). e0293801. Bibcode:2023PLoSO..1893801K. doi:10.1371/journal.pone.0293801. PMC 10651048. PMID 37967055.
- ^ Mo, J.-Y.; Fu, Q.-Y.; Yu, Y.-L.; Xu, X. (2023). "A New Titanosaurian Sauropod from the Upper Cretaceous of Jiangxi Province, Southern China". Historical Biology: 1–15. doi:10.1080/08912963.2023.2259413. S2CID 262210506.
- ^ Prieto-Márquez, A.; Wagner, J. R. (2022). "A new 'duck-billed' dinosaur (Ornithischia: Hadrosauridae) from the upper Campanian of Texas points to a greater diversity of early hadrosaurid offshoots". Cretaceous Research. 143. 105416. doi:10.1016/j.cretres.2022.105416. S2CID 253470207.
- ^ Wang, Xuri; Cau, Andrea; Wang, Zhengdong; Yu, Kaifeng; Wu, Wenhao; Wang, Yang; Liu, Yichuan (2023-06-05). "A new theropod dinosaur from the Lower Cretaceous Longjiang Formation of Inner Mongolia (China)". Cretaceous Research. 151: 105605. Bibcode:2023CrRes.15105605W. doi:10.1016/j.cretres.2023.105605. ISSN 0195-6671.
- ^ Manitkoon, Sita; Deesri, Uthumporn; Khalloufi, Bouziane; Nonsrirach, Thanit; Suteethorn, Varavudh; Chanthasit, Phornphen; Boonla, Wansiri; Buffetaut, Eric (2023). "A New Basal Neornithischian Dinosaur from the Phu Kradung Formation (Upper Jurassic) of Northeastern Thailand". Diversity. 15 (7): 851. doi:10.3390/d15070851.
- ^ Sánchez-Fenollosa, Sergio; Verdú, Francisco; Cobos, Alberto (2023). "The largest ornithopod (Dinosauria: Ornithischia) from the Upper Jurassic of Europe sheds light on the evolutionary history of basal ankylopollexians". Zoological Journal of the Linnean Society. 199 (4): 1013–1033. doi:10.1093/zoolinnean/zlad076.
- ^ Horner, J. R.; Goodwin, M. B.; Evans, D. C. (2023). "A new pachycephalosaurid from the Hell Creek Formation, Garfield County, Montana, U.S.A.". Journal of Vertebrate Paleontology. 42 (4). e2190369. doi:10.1080/02724634.2023.2190369. S2CID 258154892.
- ^ Santos-Cubedo, A.; de Santisteban, C.; Poza, B.; Meseguer, S. (2023). "A new spinosaurid dinosaur species from the Early Cretaceous of Cinctorres (Spain)". Scientific Reports. 13 (1). 6471. Bibcode:2023NatSR..13.6471S. doi:10.1038/s41598-023-33418-2. PMC 10195869. PMID 37202441.
- ^ Han, F.; Yu, Y.; Zhang, S.; Zeng, R.; Wang, X.; Cai, H.; Wu, T.; Wen, Y.; Cai, S.; Li, C.; Wu, R.; Zhao, W.; Xu, X. (2023). "Exceptional early Jurassic fossils with leathery eggs shed light on dinosaur reproductive biology". National Science Review. 11 (6): nwad258. doi:10.1093/nsr/nwad258. PMC 11067957. PMID 38707200.
- ^ a b Woodruff, D. Cary; Schott, Ryan K.; Evans, David C. (2023-11-15). "Two new species of small-bodied pachycephalosaurine (Dinosauria, Marginocephalia) from the uppermost Cretaceous of North America suggest hidden diversity in well-sampled formations". Papers in Palaeontology. 9 (6). e1535. Bibcode:2023PPal....9E1535W. doi:10.1002/spp2.1535. ISSN 2056-2799. S2CID 265261709.
- ^ Bajpai, S.; Datta, D.; Pandey, P.; Ghosh, T.; Kumar, K.; Bhattacharya, D. (2023). "Fossils of the oldest diplodocoid dinosaur suggest India was a major centre for neosauropod radiation". Scientific Reports. 13 (1). 12680. Bibcode:2023NatSR..1312680B. doi:10.1038/s41598-023-39759-2. PMC 10403599. PMID 37542094.
- ^ Hattori, S.; Shibata, M.; Kawabe, S.; Imai, T.; Nishi, H.; Azuma, Y. (2023). "New theropod dinosaur from the Lower Cretaceous of Japan provides critical implications for the early evolution of ornithomimosaurs". Scientific Reports. 13 (1). 13842. Bibcode:2023NatSR..1313842H. doi:10.1038/s41598-023-40804-3. PMC 10484975. PMID 37679444.
- ^ Longrich, Nicholas R.; Martill, David M.; Munt, Martin; Green, Mick; Penn, Mark; Smith, Shaun (2023-09-13). "Vectidromeus insularis, a new hypsilophodontid dinosaur from the Lower Cretaceous Wessex Formation of the Isle of Wight, England". Cretaceous Research. 154: 105707. doi:10.1016/j.cretres.2023.105707. ISSN 0195-6671. S2CID 261933503.
- ^ Pond, Stuart; Strachan, Sarah-Jane; Raven, Thomas J.; Simpson, Martin I.; Morgan, Kirsty; Maidment, Susannah C. R. (2023-01-01). "Vectipelta barretti, a new ankylosaurian dinosaur from the Lower Cretaceous Wessex Formation of the Isle of Wight, UK". Journal of Systematic Palaeontology. 21 (1). Bibcode:2023JSPal..2110577P. doi:10.1080/14772019.2023.2210577. ISSN 1477-2019. S2CID 259393929.
- ^ Schwarz, Daniela; Fritsch, Guido; Issever, Ahi Sema; Hildebrandt, Thomas (2023-02-14). "Description of contents of unopened bamboo corsets and crates from Quarry Ig/WJ of the Tendaguru locality (Late Jurassic, Tanzania, East Africa) as revealed by medical CT data and the potential of this data under paleontological and historical aspects". Palaeontologia Electronica. 26 (1): 1–26. doi:10.26879/1231. ISSN 1094-8074. S2CID 256977587.
- ^ Baron, M. G.; Norman, D. B.; Barrett, P. M. (2017). "A new hypothesis of dinosaur relationships and early dinosaur evolution" (PDF). Nature. 543 (7646): 501–506. Bibcode:2017Natur.543..501B. doi:10.1038/nature21700. PMID 28332513. S2CID 205254710.
- ^ Langer, M. C.; Ezcurra, M. D.; Rauhut, O. W. M.; Benton, M. J.; Knoll, F.; McPhee, B. W.; Novas, F. E.; Pol, D.; Brusatte, S. L. (2017). "Untangling the dinosaur family tree" (PDF). Nature. 551 (7678): E1–E3. Bibcode:2017Natur.551E...1L. doi:10.1038/nature24011. hdl:1983/d088dae2-c7fa-4d41-9fa2-aeebbfcd2fa3. PMID 29094688. S2CID 205260354.
- ^ Černý, D.; Simonoff, A. L. (2023). "Statistical evaluation of character support reveals the instability of higher-level dinosaur phylogeny". Scientific Reports. 13 (1). 9273. Bibcode:2023NatSR..13.9273C. doi:10.1038/s41598-023-35784-3. PMC 10247814. PMID 37286556.
- ^ Hedrick, Brandon P (2023-03-15). "Dots on a screen: The past, present, and future of morphometrics in the study of nonavian dinosaurs". The Anatomical Record. 306 (7): 1896–1917. doi:10.1002/ar.25183. PMID 36922704. S2CID 257581365.
- ^ Cullen, T. M.; Longstaffe, F. J.; Wortmann, U. G.; Huang, L.; Evans, D. C. (2023). "Anomalous 13C enrichment in Mesozoic vertebrate enamel reflects environmental conditions in a "vanished world" and not a unique dietary physiology". Paleobiology. 49 (3): 563–577. Bibcode:2023Pbio...49..563C. doi:10.1017/pab.2022.43. S2CID 255919241.
- ^ Cullen, T. M.; Cousens, B. L. (2023). "New biogeochemical insights into Mesozoic terrestrial paleoecology and evidence for omnivory in troodontid dinosaurs". GSA Bulletin. 136 (7–8): 2689–2701. doi:10.1130/B37077.1. S2CID 265241862.
- ^ Lazer, Kayla; Stout, Ian; Simpson, Edward; Wizevich, Michael; Keebler, Abigal; Hetrick, Grace (2023). "Preserved membrane on dinosaur eggshell fragments, Upper Jurassic Morrison Formation, eastern Utah". PALAIOS. 38 (1): 43–55. Bibcode:2023Palai..38...43L. doi:10.2110/palo.2022.002. S2CID 256351474.
- ^ Oussou, A.; Falkingham, P. L.; Butler, R. J.; Boumir, K.; Ouarhache, D.; Ech-charay, D.; Charrière, A.; Maidment, S. C. R. (2023). "New Middle to ?Late Jurassic dinosaur tracksites in the Central High Atlas Mountains, Morocco". Royal Society Open Science. 10 (9). 231091. Bibcode:2023RSOS...1031091O. doi:10.1098/rsos.231091. PMC 10523064. PMID 37771967.
- ^ Navarro-Lorbés, P.; Díaz-Martínez, I.; Valle-Melón, J. M.; Rodríguez, Á.; Moratalla, J. J.; Ferrer-Ventura, M.; San Juan-Palacios, R.; Torices, A. (2023). "Dinosaur swim tracks from the Lower Cretaceous of La Rioja, Spain: an ichnological approach to non-common behaviours". Cretaceous Research. 147. 105516. Bibcode:2023CrRes.14705516N. doi:10.1016/j.cretres.2023.105516. hdl:10810/61637. S2CID 257359478.
- ^ Méndez Torrez, G.; Lovera Cruz, L.; Céspedes-Llave, A. Á.; Esperante, R.; Gutiérrez Berrios, C.; Apesteguía, S. (2023). "First Jurassic to earliest Cretaceous dinosaur footprints for Bolivia at the Castellón Formation (Tacurú Group), Tarija". Historical Biology. 36 (9): 1883–1902. doi:10.1080/08912963.2023.2235373. S2CID 260024829.
- ^ Naimi, M. N.; Cherif, A.; Benyoucef, M.; Mahboubi, C. Y. (2023). "New dinosaur footprints from the 'mid'-Cretaceous (Albian-Cenomanian) series of the Ouled Nail Mounts (Algeria)". Revue de Paléobiologie, Genève. 42 (2): 273–284.
- ^ Esperante, R.; Rocha-Rodríguez, G.; McLarty, J. A.; Biaggi, R. E.; Nick, K. E.; Baltazar, H. D.; Varquera, A. C. (2023). "Diversity of dinosaur tracks and swim traces in a new site in the Upper Cretaceous El Molino formation, Torotoro National Park, Bolivia". Journal of South American Earth Sciences. 128. 104480. Bibcode:2023JSAES.12804480E. doi:10.1016/j.jsames.2023.104480. S2CID 259507937.
- ^ Yin, Ya-Lei; Xie, Fei; Zhou, Chang-Fu; Pei, Rui (2023-02-20). "Dinosaur teeth from the mid-Cretaceous Sunjiawan Formation of western Liaoning Province, China". Historical Biology. 36 (3): 631–637. doi:10.1080/08912963.2023.2179398. S2CID 257065447.
- ^ Samathi, A; Suteethorn, S; Boonjarern, T; Sutcha, K; Suteethorn, V (2023-03-24). "Dinosaur fauna from the Lower Cretaceous of Phu Kao-Phu Phan Kham, northeastern Thailand: a review and update". Palaeoworld. 33 (2): 420–438. doi:10.1016/j.palwor.2023.03.007. S2CID 257740661.
- ^ Li, Y.; Yao, H.; Yu, Y.; Foster, W. J.; Wang, C.; Zhao, L.; Xing, L. (2023). "First report of sauropod and ornithopod tracks from the Upper Cretaceous of Tibet, China". Cretaceous Research. 149. 105569. Bibcode:2023CrRes.14905569L. doi:10.1016/j.cretres.2023.105569. S2CID 258370186.
- ^ Flannery-Sutherland, J. T.; Kogan, I.; Trubin, Y. S.; Falkingham, P. L.; Winkler, A.; Donner De Sousa, D.; Krylov, K. D.; Pokhaznikova, A. A.; Derbisheva, M.; Kapitany, T.; Dudashvili, A. (2023). "Dinosaur trackways from the Upper Cretaceous Nichkesai Formation near Mayluu Suu City, Southern Tien Shan Mountains, north-western Kyrgyzstan". Royal Society Open Science. 10 (5). 230311. Bibcode:2023RSOS...1030311F. doi:10.1098/rsos.230311. PMC 10206447. PMID 37234492.
- ^ Eberth, D. A.; Evans, D. C.; Ramezani, J.; Kamo, S. L.; Brown, C. M.; Currie, P. J.; Braman, D. R. (2023). "Calibrating geologic strata, dinosaurs, and other fossils at Dinosaur Provincial Park (Alberta, Canada) using a new CA-ID-TIMS U–Pb geochronology". Canadian Journal of Earth Sciences. 60 (12): 1627–1646. Bibcode:2023CaJES..60.1627E. doi:10.1139/cjes-2023-0037. S2CID 259622192.
- ^ Tanaka, K.; Zelenitsky, D. K.; Therrien, F.; Lee, Y.-N.; Kubota, K.; Kobayashi, K.; Funston, G.; Tsogtbaatar, K. (2023). "Description and review of non-avian dinosaur eggs from Cretaceous deposits of the Mongolian Gobi Desert". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 176–210. ISBN 978-89-5708-358-1.
- ^ Amiot, R.; Golovneva, L. B.; Godefroit, P.; Goedert, J.; Garcia, G.; Lécuyer, C.; Fourel, F.; Herman, A. B.; Spicer, R. A. (2023). "High-Latitude Dinosaur Nesting Strategies during the Latest Cretaceous in North-Eastern Russia". Diversity. 15 (4). 565. doi:10.3390/d15040565.
- ^ Khosa, A.; Spencer, S. G (2023). "Review of the Cretaceous dinosaurs from India and their paleobiogeographic significance". Acta Geologica Polonica. 74: 707–740. doi:10.24425/agp.2023.145623. S2CID 262165191.
- ^ Garcia, M. S.; Cabreira, S. F.; Silva, L. R.; Pretto, F. A.; Müller, R. T. (2023). "A saurischian (Archosauria, Dinosauria) ilium from the Upper Triassic of southern Brazil and the rise of Herrerasauria". The Anatomical Record. 307 (4): 1011–1024. doi:10.1002/ar.25342. PMID 37971103. S2CID 265262541.
- ^ Silva, F. O.; Martinelli, A. G.; Ferigolo, J.; Ribeiro, A. M. (2023). "A new herrerasaurid dinosaur record from southern Brazil (Upper Triassic) and its faunal association". Revista Brasileira de Paleontologia. 26 (2): 97–113. doi:10.4072/rbp.2023.2.02. S2CID 259942523.
- ^ Xing, Lida; Wang, Yongdong; Lockley, Martin G.; Klein, Hendrik; Liu, Chang; Persons, W. Scott (2023-01-02). "The first record of dinosaur track from Hubei Province, Central China". Historical Biology. 36 (2): 425–430. doi:10.1080/08912963.2022.2164494. ISSN 0891-2963. S2CID 255671833.
- ^ Lei, R.; Tschopp, E.; Hendrickx, C.; Wedel, M. J.; Norell, M.; Hone, D. W. E. (2023). "Bite and tooth marks on sauropod dinosaurs from the Morrison Formation". PeerJ. 11. e16327. doi:10.7717/peerj.16327. PMC 10655710. PMID 38025762.
- ^ D'Emic, M. D.; O'Connor, P. M.; Sombathy, R. S.; Cerda, I.; Pascucci, T. R.; Varricchio, D.; Pol, D.; Dave, A.; Coria, R. A.; Curry Rogers, K. A. (2023). "Developmental strategies underlying gigantism and miniaturization in non-avialan theropod dinosaurs". Science. 379 (6634): 811–814. Bibcode:2023Sci...379..811D. doi:10.1126/science.adc8714. PMID 36821658. S2CID 257103111.
- ^ Henderson, D. M. (2023). "Growth constraints set an upper limit to theropod dinosaur body size". The Science of Nature. 110 (1). 4. Bibcode:2023SciNa.110....4H. doi:10.1007/s00114-023-01832-1. PMID 36715746. S2CID 256362332.
- ^ Cullen, T. M.; Larson, D. W.; Witton, M. P.; Scott, D.; Maho, T.; Brink, K. S.; Evans, D. C.; Reisz, D. (2023). "Theropod dinosaur facial reconstruction and the importance of soft tissues in paleobiology". Science. 379 (6639): 1348–1352. Bibcode:2023Sci...379.1348C. doi:10.1126/science.abo7877. PMID 36996202. S2CID 257836765.
- ^ Barsbold, R. (2023). "Late carnivorous dinosaurs: hand modifications, evolution, and ecology". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 120–129. ISBN 978-89-5708-358-1.
- ^ Kirmse, J. P. S.; Benton, M. J.; Hildebrandt, C.; Langer, M. C.; Marsola, J. C. A. (2023). "A Coelophysoidea (Dinosauria, Theropoda) femur from the Tytherington fissures (Rhaetian, Late Triassic), Bristol, UK". Proceedings of the Geologists' Association. 134 (5–6): 562–572. Bibcode:2023PrGA..134..562K. doi:10.1016/j.pgeola.2023.07.005. S2CID 260875074.
- ^ Peng, S.; Liu, J.; Benton, M. J.; Jin, X.; Shi, Z. (2023). "The first dinosaurs in China: Dating Late Triassic footprint fossils from the Sichuan Basin". Gondwana Research. 117: 261–273. Bibcode:2023GondR.117..261P. doi:10.1016/j.gr.2023.02.003. S2CID 256671291.
- ^ Zhang, Z.-C.; Wang, T.; You, H.-L. (2023). "A New Specimen of Sinosaurus triassicus (Dinosauria: Theropoda) from the Early Jurassic of Lufeng, Yunnan, China". Historical Biology. 36 (4): 857–871. doi:10.1080/08912963.2023.2190760. S2CID 257747661.
- ^ Ezcurra, M. D.; Marke, D.; Walsh, S. A.; Brusatte, S. L. (2023). "A revision of the 'coelophysoid-grade' theropod specimen from the Lower Jurassic of the Isle of Skye (Scotland)" (PDF). Scottish Journal of Geology. 59 (1–2): 012. Bibcode:2023ScJG...59...12E. doi:10.1144/sjg2023-012. hdl:20.500.11820/c9cde9ec-b458-42d3-a002-2b03ec6dbe54. S2CID 264343748.
- ^ Sharma, A.; Hendrickx, C.; Singh, S. (2023). "First theropod record from the Marine Bathonian of Jaisalmer Basin, Tethyan Coast of Gondwanan India". Rivista Italiana di Paleontologia e Stratigrafia. 129 (1): 49–64. doi:10.54103/2039-4942/18306. S2CID 256347914.
- ^ Li, Y.; Jiang, S.; Yan, F.; Ma, Y.; Wang, X. (2023). "The first record of Lower Cretaceous theropod tracks in Turpan-Hami Basin, Xinjiang, northwestern China". Historical Biology: 1–6. doi:10.1080/08912963.2023.2259419. S2CID 263182628.
- ^ Leonardi, G.; Fernandes, M. A.; Carvalho, I. S.; Schutzer, J. B.; Silva, R. C. (2023). "Farlowichnus rapidus new ichnogen., new ichnosp.: A speedy and small theropod in the Early Cretaceous Botucatu paleodesert (Paraná Basin), Brazil". Cretaceous Research. 153. 105720. doi:10.1016/j.cretres.2023.105720. S2CID 263317033.
- ^ Lockley, M. G.; McCrea, R. T.; Buckley, L. G.; Lim, J. D.; Matthews, N. A.; Breithaupt, B. H.; Houck, K. J.; Gierliński, G. D.; Surmik, D.; Kim, K. S.; Xing, L.; Kong, D. Y.; Cart, K.; Martin, J.; Hadden, G. (2016). "Theropod courtship: large scale physical evidence of display arenas and avian-like scrape ceremony behaviour by Cretaceous dinosaurs". Scientific Reports. 6. 18952. Bibcode:2016NatSR...618952L. doi:10.1038/srep18952. PMC 4704466. PMID 26741567.
- ^ Moklestad, T.; Lucas, S. G. (2023). "Elongated, non-avian theropod tracks (pes scrapes) in the Cretaceous of Colorado may represent failed attempts at nest building". New Mexico Museum of Natural History and Science Bulletin. 94: 443–455.
- ^ Souza-Júnior, A. L.; Candeiro, C. R. A.; Vidal, L. S.; Brusatte, S. L.; Mortimer, M. (2023). "Abelisauroidea (Theropoda, Dinosauria) from Africa: a review of the fossil record". Papéis Avulsos de Zoologia. 63. e202363019. doi:10.11606/1807-0205/2023.63.019. S2CID 259553222.
- ^ Averianov, A. O.; Lopatin, A. V. (2023). "A long-necked theropod from the Lower Cretaceous of Western Siberia, Russia". Journal of Vertebrate Paleontology. 42 (6). e2216761. doi:10.1080/02724634.2023.2216761. S2CID 259675775.
- ^ Averianov, A. O.; Skutschas, P. P.; Atuchin, A. A.; Slobodin, D. A.; Feofanova, O. A.; Vladimirova, O. N. (2024). "The last ceratosaur of Asia: a new noasaurid from the Early Cretaceous Great Siberian Refugium". Proceedings of the Royal Society B: Biological Sciences. 291 (2023). 20240537. doi:10.1098/rspb.2024.0537. PMC 11285863. PMID 38747705.
- ^ Barbosa, G. G.; Langer, M. C.; de Oliveira Martins, N.; Montefeltro, F. C. (2023). "Assessing the palaeobiology of Vespersaurus paranaensis (Theropoda, Noasauridae), Cretaceous, Bauru Basin – Brazil, using Finite Element Analysis". Cretaceous Research. 150. 105594. Bibcode:2023CrRes.15005594B. doi:10.1016/j.cretres.2023.105594. S2CID 258952922.
- ^ Amudeo-Plaza, J.; Soto-Acuña, S.; Ugalde, R.; Martínez, P.; Rubilar-Rogers, D. (2023). "Reassessment of theropod material from Pichasca, Northern Chile: Presence of Abelisauridae (Theropoda: Ceratosauria) from the Quebrada La Totora Beds (Albian - Turonian)". Journal of South American Earth Sciences. 129. 104494. Bibcode:2023JSAES.12904494A. doi:10.1016/j.jsames.2023.104494. S2CID 260074394.
- ^ Paulina-Carabajal, A.; Ulloa-Guaiquín, K.; Filippi, L. S.; Méndez, A. H.; Lee, Y.-N. (2023). "First record of an abelisaurid (Dinosauria, Theropoda) natural endocast, and comments on skull roof ornamentation". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 130–139. ISBN 978-89-5708-358-1.
- ^ Longrich, N. R.; Isasmendi, E.; Pereda-Suberbiola, X.; Jalil, N.-E. (2023). "New fossils of Abelisauridae (Dinosauria: Theropoda) from the upper Maastrichtian of Morocco, North Africa". Cretaceous Research. 152. 105677. Bibcode:2023CrRes.15205677L. doi:10.1016/j.cretres.2023.105677. S2CID 261090591.
- ^ Baiano, M. A.; Coria, R.; Chiappe, L. M.; Zurriaguz, V.; Coria, L. (2023). "Osteology of the axial skeleton of Aucasaurus garridoi: phylogenetic and paleobiological inferences". PeerJ. 11. e16236. doi:10.7717/peerj.16236. PMC 10655716. PMID 38025666.
- ^ Lacerda, M. B. S.; Bittencourt, J. S.; Hutchinson, J. R. (2023). "Macroevolutionary patterns in the pelvis, stylopodium and zeugopodium of megalosauroid theropod dinosaurs and their importance for locomotor function". Royal Society Open Science. 10 (8). 230481. Bibcode:2023RSOS...1030481L. doi:10.1098/rsos.230481. PMC 10427828. PMID 37593714.
- ^ Lacerda, M. B. S.; Bittencourt, J. S.; Hutchinson, J. R. (2023). "Reconstruction of the pelvic girdle and hindlimb musculature of the early tetanurans Piatnitzkysauridae (Theropoda, Megalosauroidea)". Journal of Anatomy. 244 (4): 557–593. doi:10.1111/joa.13983. PMC 10941590. PMID 38037880.
- ^ Terras, R.; Carbonera, M.; Budke, G.; Leite, K. J. G. (2023). "Spinosauridae family (Dinosauria: Theropoda): taxonomy, paleobiogeography and paleoecology (a revision)". Paleodest. 37 (77): 14–54. doi:10.4072/paleodest.2022.37.77.02. S2CID 259731689.
- ^ Sharma, A.; Novas, F. E.; Singh, S. (2023). "First Jurassic evidence of a possible spinosaurid pedal ungual from the Jaisalmer Basin, India". Rivista Italiana di Paleontologia e Stratigrafia. 129 (3): 653–670. doi:10.54103/2039-4942/20032.
- ^ Barker, C. T.; Naish, D.; Gostling, N. J. (2023). "Isolated tooth reveals hidden spinosaurid dinosaur diversity in the British Wealden Supergroup (Lower Cretaceous)". PeerJ. 11. e15453. doi:10.7717/peerj.15453. PMC 10239232. PMID 37273543.
- ^ Barker, C.T.; Naish, D.; Trend, J.; Michels, L.V.; Witmer, L.; Ridgley, R.; Rankin, K.; Clarkin, C.; Schneider, P.; Gostling, N.J. (2023). "Modified skulls but conservative brains? The palaeoneurology and endocranial anatomy of baryonychine dinosaurs (Theropoda: Spinosauridae)". Journal of Anatomy. 242 (6): 1124–1145. doi:10.1111/joa.13837. PMC 10184548. PMID 36781174. S2CID 256845477.
- ^ Lacerda, M. B. S.; Aragão, P. R. L.; Vieira, F. S.; Sales, M. A. F.; Liparini, A. (2023). "On the first Baryonychinae (Theropoda, Spinosauridae) teeth from South America". Zootaxa. 5264 (4): 526–544. doi:10.11646/zootaxa.5264.4.4. PMID 37518033. S2CID 258210733.
- ^ Schade, M.; Rauhut, O. W. M.; Foth, C.; Moleman, O.; Evers, S. W. (2023). "A reappraisal of the cranial and mandibular osteology of the spinosaurid Irritator challengeri (Dinosauria: Theropoda)". Palaeontologia Electronica. 26 (2). 26.2.17. doi:10.26879/1242.
- ^ Smith, R; Martill, D (2023-02-07). "An unusual dental pathology in a tooth of Spinosaurus (Dinosauria, Theropoda) from the mid-Cretaceous of Morocco". Cretaceous Research. 146: 105499. Bibcode:2023CrRes.14605499S. doi:10.1016/j.cretres.2023.105499. S2CID 256685951.
- ^ Aranciaga Rolando, A. M.; Novas, F. E.; Calvo, J. O.; Porfiri, J. D.; Dos Santos, D. D.; Lamanna, M. C. (2023). "Reconstruction of the pectoral girdle and forelimb musculature of Megaraptora (Dinosauria: Theropoda)". The Anatomical Record. 306 (7): 1804–1823. doi:10.1002/ar.25128. PMID 36647300. S2CID 255939861.
- ^ Samathi, Adun; Weluwanarak, Jakkrapat; Duanyai, Punyawee; Kaikaew, Siripat; Suteethorn, Suravech (2023-01-13). "An unusual metatarsal of theropod dinosaur from the lower cretaceous of Thailand: the first detailed study of paleopathology in Megaraptora". Historical Biology. 36 (3): 467–472. doi:10.1080/08912963.2023.2166833. ISSN 0891-2963. S2CID 255902629.
- ^ Kotevski, J.; Duncan, R. J.; Pentland, A. H.; Rule, J. P.; Vickers-Rich, P.; Rich, T. H.; Fitzgerald, E. M. G.; Evans, A. R.; Poropat, S. F. (2023). "A megaraptorid (Dinosauria: Theropoda) frontal from the upper Strzelecki Group (Lower Cretaceous) of Victoria, Australia". Cretaceous Research. 154. 105769. doi:10.1016/j.cretres.2023.105769.
- ^ Herculano-Houzel, S. (2023). "Theropod dinosaurs had primate-like numbers of telencephalic neurons". Journal of Comparative Neurology. 531 (9): 962–974. doi:10.1002/cne.25453. PMID 36603059. S2CID 249994109.
- ^ Rodrigo Pérez Ortega (2023-01-10). "Some dinos may have been as brainy as modern primates, controversial study argues". Science.org.
- ^ Caspar, K. R.; Gutiérrez-Ibáñez, C.; Bertrand, O. C.; Carr, T.; Colbourne, J. A. D.; Erb, A.; George, H.; Holtz, T. R.; Naish, D.; Wylie, D. R.; Hurlburt, G. R. (2024). "How smart was T. rex? Testing claims of exceptional cognition in dinosaurs and the application of neuron count estimates in palaeontological research". The Anatomical Record. doi:10.1002/ar.25459. PMID 38668805.
- ^ Pahl, Cameron C.; Ruedas, Luis A. (2021). "Carnosaurs as Apex Scavengers: Agent-based simulations reveal possible vulture analogues in late Jurassic Dinosaurs". Ecological Modelling. 458: 109706. Bibcode:2021EcMod.45809706P. doi:10.1016/j.ecolmodel.2021.109706. ISSN 0304-3800.
- ^ Kane, Adam; Healy, Kevin; Ruxton, Graeme D. (2023). "Was Allosaurus really predominantly a scavenger?". Ecological Modelling. 476: 110247. Bibcode:2023EcMod.47610247K. doi:10.1016/j.ecolmodel.2022.110247. ISSN 0304-3800. S2CID 254712679.
- ^ Pahl, Cameron C.; Ruedas, Luis A. (2023-03-01). "Allosaurus was predominantly a scavenger". Ecological Modelling. 477: 110261. Bibcode:2023EcMod.47710261P. doi:10.1016/j.ecolmodel.2022.110261. ISSN 0304-3800. S2CID 255661337.
- ^ Lessner, E. J.; Cranor, C.; Hunt-Foster, R.; Holliday, C. M. (2023). "Endocranial anatomy of Allosaurus supports neural trends among non-avian theropod dinosaurs". Journal of Vertebrate Paleontology. 43 (1). e2236161. doi:10.1080/02724634.2023.2236161. S2CID 261155906.
- ^ Yu, Y.; Yi, H.; Wang, S.; Pei, R.; Zhang, C.; Xu, X. (2023). "A Jurassic Tibetan theropod tooth reveals dental convergency and its implication for identifying fragmentary fossils". The Innovation Geoscience. 1 (3). doi:10.59717/j.xinn-geo.2023.100040.
- ^ Carrano, M. T. (2023). "First definitive record of Acrocanthosaurus (Theropoda: Carcharodontosauridae) in the Lower Cretaceous of eastern North America". Cretaceous Research. 157. 105814. doi:10.1016/j.cretres.2023.105814. S2CID 266645706.
- ^ Zhang, J.; Du, B.; Lin, S.; Peng, J.; Li, A.; Zhang, M.; Ma, G.; Hui, J.; Jiaoba, D.; Liu, G. (2023). "Downy feather fossils from the Lower Cretaceous of the Jiuquan Basin, Gansu Province, Northwest China". Cretaceous Research. 151. 105653. Bibcode:2023CrRes.15105653Z. doi:10.1016/j.cretres.2023.105653. S2CID 259514727.
- ^ Johnson-Ransom, E.; Li, F.; Xu, X.; Ramos, R.; Midzuk, A. J.; Thon, U.; Atkins-Weltman, K.; Snively, E. (2023). "Comparative cranial biomechanics reveal that Late Cretaceous tyrannosaurids exerted relatively greater bite force than in early-diverging tyrannosauroids". The Anatomical Record. 307 (5): 1897–1917. doi:10.1002/ar.25326. PMID 37772730. S2CID 263224803.
- ^ Carr, T. D. (2023). "A reappraisal of tyrannosauroid fossils from the Iren Dabasu Formation (Coniacian–Campanian), Inner Mongolia, People's Republic of China". Journal of Vertebrate Paleontology. 42 (5). e2199817. doi:10.1080/02724634.2023.2199817. S2CID 259005327.
- ^ Yun, C. G. (2023). "A tyrannosaurid pedal ungual from the Williams Fork Formation (Campanian) of Colorado and its implications for the biogeography of Laramidian dinosaurs". Acta Geologica Polonica. 73 (1). e2199817. doi:10.24425/agp.2022.140433. S2CID 260049018.
- ^ Therrien, F.; Zelenitsky, D. K.; Tanaka, K.; Voris, J. T.; Erickson, G. M.; Currie, P. J.; DeBuhr, C. L.; Kobayashi, Y. (2023). "Exceptionally preserved stomach contents of a young tyrannosaurid reveal an ontogenetic dietary shift in an iconic extinct predator". Science Advances. 9 (49): eadi0505. Bibcode:2023SciA....9I.505T. doi:10.1126/sciadv.adi0505. PMC 10846869. PMID 38064561.
- ^ Coppock, C.; Currie, P. J. (2023). "Additional Albertosaurus sarcophagus (Tyrannosauridae, Albertosaurinae) material from the Danek Bonebed of Edmonton, Alberta, Canada with evidence of cannibalism". Canadian Journal of Earth Sciences. 61 (3): 401–407. doi:10.1139/cjes-2023-0055. S2CID 266279287.
- ^ Warshaw, E. A.; Fowler, D. W. (2022). "A transitional species of Daspletosaurus Russell, 1970 from the Judith River Formation of eastern Montana". PeerJ. 10. e14461. doi:10.7717/peerj.14461. PMC 9703990. PMID 36452080.
- ^ Scherer, C. R.; Voiculescu-Holvad, C. (2023). "Re-analysis of a dataset refutes claims of anagenesis within Tyrannosaurus-line tyrannosaurines (Theropoda, Tyrannosauridae)". Cretaceous Research. 155. 105780. doi:10.1016/j.cretres.2023.105780.
- ^ Warshaw, E. A.; Barrera Guevara, D.; Fowler, D. W. (2024). "Anagenesis and the tyrant pedigree: a response to "Re-analysis of a dataset refutes claims of anagenesis within Tyrannosaurus-line tyrannosaurines (Theropoda, Tyrannosauridae)"". Cretaceous Research. 163. 105957. Bibcode:2024CrRes.16305957W. doi:10.1016/j.cretres.2024.105957.
- ^ Fiorillo, A. R.; Kobayashi, Y.; McCarthy, P. J.; Stelson, L.; Schwing, E. (2023). "On the significance of a Late Cretaceous tyrannosaur track from Aniakchak National Monument (Chignik Formation, Campanian – Maastrichtian), southwestern Alaska". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 211–221. ISBN 978-89-5708-358-1.
- ^ Hodnett, John-Paul; Carrano, Matthew; Santucci, Vincent; Tweet, Justin; Visaggi, Christy (2023). "A Tyrannosaur (Dinosauria; Theropoda; Tyrannosauridae) from the Late Cretaceous (Maastrichtian) Harebell Formation of Yellowstone National Park, Wyoming". New Mexico Museum of Natural History & Science Bulletin. 94: 233–238.
- ^ Anné, J.; Canoville, A.; Edwards, N. P.; Schweitzer, M. H.; Zanno, L. E. (2023). "Independent Evidence for the Preservation of Endogenous Bone Biochemistry in a Specimen of Tyrannosaurus rex". Biology. 12 (2). 264. doi:10.3390/biology12020264. PMC 9953530. PMID 36829540.
- ^ Qin, Z.; Liao, C.-C.; Benton, M. J.; Rayfield, E. J. (2023). "Functional space analyses reveal the function and evolution of the most bizarre theropod manual unguals". Communications Biology. 6 (1). 181. doi:10.1038/s42003-023-04552-4. PMC 9935540. PMID 36797463.
- ^ Pintore, R.; Cornette, R.; Houssaye, A.; Allain, R. (2023). "Femora from an exceptionally large population of coeval ornithomimosaurs yield evidence of sexual dimorphism in extinct theropod dinosaurs". eLife. 12. e83413. doi:10.7554/eLife.83413. PMC 10264075. PMID 37309177.
- ^ Chamberlain, JA; Knoll, K; Sertich, J (2023-02-07). "Non-avian theropod phalanges from the marine Fox Hills Formation (Maastrichtian), western South Dakota, USA". PeerJ. 11: e14665. doi:10.7717/peerj.14665/supp-1. PMC 9912944. PMID 36778140.
- ^ Averianov, A.; Skutschas, P.; Bolotsky, Y.; Bolotsky, I. (2023). "First find of an ornithomimid theropod dinosaur in the Upper Cretaceous of the Russian Far East". Biological Communications. 68 (4): 253–260. doi:10.21638/spbu03.2023.405.
- ^ Qin, Z.; Zhao, Q.; Choiniere, J. N.; Clark, J. M.; Benton, M.J.; Xu, X. (2021). "Growth and miniaturization among alvarezsauroid dinosaurs". Current Biology. 31 (16): 3687–3693.e5. Bibcode:2021CBio...31E3687Q. doi:10.1016/j.cub.2021.06.013. PMID 34233160. S2CID 235752037.
- ^ Averianov, A.; Skutschas, P.; Lopatin, A. (2023). "Ontogeny and miniaturization of Alvarezsauridae (Dinosauria, Theropoda)". Biological Communications. 68 (2): 65–73. doi:10.21638/spbu03.2023.201. S2CID 259606242.
- ^ Senter, P. J. (2023). "Restudy of shoulder motion in the theropod dinosaur Mononykus olecranus (Alvarezsauridae)". PeerJ. 11. e16605. doi:10.7717/peerj.16605. PMC 10704983. PMID 38077415.
- ^ Wills, S.; Underwood, C. J.; Barrett, P. M. (2023). "Machine learning confirms new records of maniraptoran theropods in Middle Jurassic UK microvertebrate faunas". Papers in Palaeontology. 9 (2). e1487. Bibcode:2023PPal....9E1487W. doi:10.1002/spp2.1487. S2CID 258160569.
- ^ Smith, D. K. (2023). "Hindlimb Musculature of the Lower Cretaceous (Barremian) Therizinosaur Falcarius utahensis (Maniraptora, Theropoda) with Implications for Evolution, Stance, and Stride". Cretaceous Research. 149. 105557. Bibcode:2023CrRes.14905557S. doi:10.1016/j.cretres.2023.105557. S2CID 258177949.
- ^ Smith, D. K.; Gillette, D. D. (2023). "Reconstruction of soft non-contractile tissue in the derived therizinosaur Nothronychus: the interplay of soft tissue and stress on hindlimb ossification and posture". Journal of Morphology. 284 (5). e21579. doi:10.1002/jmor.21579. PMID 36929022. S2CID 257583565.
- ^ Uno, Yurika; Hirasawa, Tatsuya (2023). "Origin of the propatagium in non-avian dinosaurs". Zoological Letters. 9 (1): 4. doi:10.1186/s40851-023-00204-x. PMC 9951497. PMID 36823531.
- ^ Hogan, Jason D.; Varricchio, David J. (2023). "Chthonic severance: dinosaur eggs of the Mesozoic, the significance of partially buried eggs and contact incubation precursors". Philosophical Transactions of the Royal Society B: Biological Sciences. 378 (1884). doi:10.1098/rstb.2022.0144. PMC 10331910. PMID 37427474.
- ^ Averianov, A. O.; Lopatin, A. V. (2023). "New Data on Late Cretaceous Theropods from the Bostobe Formation of Northeastern Aral Sea Region (Kazakhstan)". Doklady Earth Sciences. 510 (1): 303–306. Bibcode:2023DokES.510..303A. doi:10.1134/S1028334X23600123. S2CID 258789491.
- ^ Voris, J. T.; Zelenitsky, D. K.; Therrien, F. (2023). "Caenagnathids (Theropoda, Oviraptorosauria) from the uppermost Maastrichtian of the Scollard Formation of Alberta, Canada". Cretaceous Research. 153. 105708. doi:10.1016/j.cretres.2023.105708. S2CID 261779584.
- ^ Wick, S. L.; Lehman, T. M.; Fortner, J. D. (2023). "New caenagnathid (Theropoda: Oviraptorosauria) dinosaur specimens from middle and upper Campanian strata of West Texas". Geobios. 82: 93–116. doi:10.1016/j.geobios.2023.08.002. S2CID 265209719.
- ^ Hogan, Jason D. (2023). "The egg-thief architect: experimental oviraptorosaur nesting physiology, the possibility of adult-mediated incubation, and the feasibility of indirect contact incubation". Paleobiology. 50: 108–122. doi:10.1017/pab.2023.19. S2CID 260860462.
- ^ Martin, Damien; Currie, Philip J.; Kundrát, Martin (2023). "Variability of bone microstructure and growth lines in the evolution of troodontids and dromaeosaurids". Acta Zoologica. 105 (2): 135–175. doi:10.1111/azo.12467. S2CID 258655244.
- ^ Yang, L.; Li, X.; Chen, J.; Reisz, R. R. (2023). "First Discovery of Large-bodied Dromaeosaurid Fossil Materials (Dinosauria: Theropoda) from the Upper Cretaceous Quantou Formation, Songliao Basin, Northeast China". Cretaceous Research. 153. 105711. doi:10.1016/j.cretres.2023.105711. S2CID 262181571.
- ^ Croudace, A. D.; Shen, C.; Lü, J.; Brusatte, S. L.; Vinther, J. (2023). "Iridescent plumage in a juvenile dromaeosaurid theropod dinosaur". Acta Palaeontologica Polonica. 68 (2): 213–225. doi:10.4202/app.01004.2022. hdl:20.500.11820/6f4df584-274a-45d9-a09b-487425ff9569. S2CID 259423800.
- ^ Malafaia, Elisabete; Escaso, Fernando; Coria, Rodolfo A.; Ortega, Francisco (2023-01-19). "An Eudromaeosaurian Theropod from Lo Hueco (Upper Cretaceous. Central Spain)". Diversity. 15 (2): 141. doi:10.3390/d15020141. ISSN 1424-2818.
- ^ Averianov, A. O.; Lopatin, A. V. (2023). "New data on Kansaignathus sogdianus, a dromaeosaurid theropod from the Upper Cretaceous of Tajikistan". Cretaceous Research. 147. 105524. Bibcode:2023CrRes.14705524A. doi:10.1016/j.cretres.2023.105524. S2CID 257453407.
- ^ Czepiński, Ł. (2023). "Skull of a dromaeosaurid dinosaur Shri devi from the Upper Cretaceous of the Gobi Desert suggests convergence to the North American forms". Acta Palaeontologica Polonica. 68 (2): 227–243. doi:10.4202/app.01065.2023. S2CID 259441055.
- ^ Tada, S.; Tsuihiji, T.; Matsumoto, R.; Hanai, T.; Iwami, Y.; Tomita, N.; Sato, H.; Tsogtbaatar, K. (2023). "Evolutionary process toward avian-like cephalic thermoregulation system in Theropoda elucidated based on nasal structures". Royal Society Open Science. 10 (4). 220997. Bibcode:2023RSOS...1020997T. doi:10.1098/rsos.220997. PMC 10090882. PMID 37063996.
- ^ Martin, D.; Caizhi, S.; Kundrát, M. (2023). "Intraindividual variability of the histological, chronological and growth patterns in post-cranial elements of Liaoningvenator curriei (Paraves: Troodontidae)". Historical Biology: 1–21. doi:10.1080/08912963.2023.2242911. S2CID 260713781.
- ^ Tagliavento, M.; Davies, A. J.; Bernecker, M.; Staudigel, P. T.; Dawson, R. R.; Dietzel, M.; Götschl, K.; Guo, W.; Schulp, A. S.; Therrien, F.; Zelenitsky, D. K.; Gerdes, A.; Müller, W.; Fiebig, J. (2023). "Evidence for heterothermic endothermy and reptile-like eggshell mineralization in Troodon, a non-avian maniraptoran theropod". Proceedings of the National Academy of Sciences of the United States of America. 120 (15). e2213987120. Bibcode:2023PNAS..12013987T. doi:10.1073/pnas.2213987120. PMC 10104568. PMID 37011196.
- ^ Lockley, Martin G.; Lallensack, Jens N.; Sciscio, Lara; Bordy, Emese M. (2023). "The early Mesozoic saurischian trackways Evazoum and Otozoum: implications for 'prosauropod' (basal sauropodomorph) gaits". Historical Biology. 36 (2): 406–424. doi:10.1080/08912963.2022.2163170. S2CID 256253243.
- ^ Moro, D.; Damke, L. V. S.; Müller, R. T.; Kerber, L.; Pretto, F. A. (2023). "An unusually robust specimen attributed to Buriolestes schultzi (Dinosauria: Sauropodomorpha) from the Late Triassic of southern Brazil". The Anatomical Record. 307 (4): 1025–1059. doi:10.1002/ar.25319. PMID 37725325. S2CID 262062104.
- ^ Sciscio, L.; Bordy, E. M.; Lockley, M. G.; Abrahams, M. G. (2023). "Basal sauropodomorph locomotion: ichnological lessons from the Late Triassic trackways of bipeds and quadrupeds (Elliot Formation, main Karoo Basin)". PeerJ. 11. e15970. doi:10.7717/peerj.15970. PMC 10542822. PMID 37790620.
- ^ Chapelle, K. E. J.; Botha, J.; Choiniere, J. N. (2023). "Osteohistology reveals the smallest adult Jurassic sauropodomorph". Royal Society Open Science. 10 (6). 221565. Bibcode:2023RSOS...1021565C. doi:10.1098/rsos.221565. PMC 10265025. PMID 37325591.
- ^ Ezcurra, M. D.; Müller, R. T.; Novas, F. E.; Chatterjee, S. (2023). "Osteology of the sauropodomorph dinosaur Jaklapallisaurus asymmetricus from the Late Triassic of central India". The Anatomical Record. 307 (4): 1093–1112. doi:10.1002/ar.25359. PMID 38088472. S2CID 266224479.
- ^ Müller, Rodrigo T.; Garcia, Maurício S.; Bem, Fabiula P.; Damke, Lísie V. S.; Fonseca, André O.; Da-Rosa, Átila A. S. (2023-07-06). "On a skeletally immature individual of Unaysaurus tolentinoi (Dinosauria: Sauropodomorpha) from the upper Triassic of southern Brazil". The Anatomical Record. 307 (4): 1071–1083. doi:10.1002/ar.25285. ISSN 1932-8486. PMID 37409690. S2CID 259352685.
- ^ Regalado Fernández, O. R.; Stöhr, H.; Kästle, B.; Werneburg, I. (2023). "Diversity and taxonomy of the Late Triassic sauropodomorphs (Saurischia, Sauropodomorpha) stored in the Palaeontological Collection of Tübingen, Germany, historically referred to Plateosaurus". European Journal of Taxonomy (913): 1–88. doi:10.5852/ejt.2023.913.2375.
- ^ Aureliano, T.; Ghilardi, A. M.; Müller, R. T.; Kerber, L.; Fernandes, M. A.; Ricardi-Branco, F.; Wedel, M. J. (2023). "The origin of an invasive air sac system in sauropodomorph dinosaurs". The Anatomical Record. 307 (4): 1084–1092. doi:10.1002/ar.25209. PMID 36971057. S2CID 257764523.
- ^ Bem, F. P.; Müller, R. T. (2023). "First record of Macrocollum itaquii (Dinosauria: Sauropodomorpha) outside the type locality and its biostratigraphic significance". Historical Biology: 1–14. doi:10.1080/08912963.2023.2269404. S2CID 264299997.
- ^ Moopen, A.; Matiwane, A.; Viglietti, P. A.; Choiniere, J. N. (2023). "Anatomy and phylogenetic relationships of a possible lessemsaurid with associated plant fossils from the lower part of the Elliot Formation". Palaeontologia Africana. 56: 190–212. hdl:10539/37131.
- ^ D'Emic, M. D. (2023). "The evolution of maximum terrestrial body mass in sauropod dinosaurs". Current Biology. 33 (9): R349–R350. Bibcode:2023CBio...33R.349D. doi:10.1016/j.cub.2023.02.067. PMID 37160089. S2CID 258560646.
- ^ Hanta, R.; Sekiya, T.; Shibata, M.; Naksri, W.; Tucker, R. T. (2023). "Hatchling and Early Juvenile of Early Sauropod from the Early Middle Jurassic Nam Phong Formation, Chaiyaphum Province, Northeastern Thailand". Paleontological Research. 28 (3): 222–239. doi:10.2517/PR230002. S2CID 261448098.
- ^ Wei, Xue-Fang; Wang, Qi-Yu; An, Xian-Yin; Wang, Bao-Di; Zhang, Yu-Jie; Mou, Chuang-Long; Li, Yong; Wang, Dong-Bing; Ma, Waisum; Kundrát, Martin (2023-02-11). "New sauropod remains from the Middle Jurassic Dongdaqiao Formation of Qamdo, eastern Tibet". Palaeoworld. 33 (3): 744–752. doi:10.1016/j.palwor.2023.02.002. S2CID 256813538.
- ^ An, X.; Xu, X.; Han, F.; Sullivan, C.; Wang, Q.; Li, Y.; Wang, D.; Wang, B.; Hu, J. (2023). "A new juvenile sauropod specimen from the Middle Jurassic Dongdaqiao Formation of East Tibet". PeerJ. 11. e14982. doi:10.7717/peerj.14982. PMC 10039653. PMID 36974139.
- ^ Moore, Andrew J.; Barrett, Paul M.; Upchurch, Paul; Liao, Chun-Chi; Ye, Yong; Hao, Baoqiao; Xu, Xing (2023-01-01). "Re-assessment of the Late Jurassic eusauropod Mamenchisaurus sinocanadorum Russell and Zheng, 1993, and the evolution of exceptionally long necks in mamenchisaurids". Journal of Systematic Palaeontology. 21 (1): 2171818. Bibcode:2023JSPal..2171818M. doi:10.1080/14772019.2023.2171818. ISSN 1477-2019. S2CID 257573094.
- ^ Milàn, J.; Mateus, O. (2023). "A Turiasaurian (Dinosauria, Sauropoda) Tooth from the Pliensbachian Hasle Formation of Bornholm, Denmark, Shows an Early Jurassic Origin of the Turiasauria". Diversity. 16 (1). 12. doi:10.3390/d16010012.
- ^ Garderes, J. P.; Gallina, P. A.; Whitlock, J. A.; Toledo, N. (2023). "Cranial osteology of Bajadasaurus pronuspinax (Sauropoda, Dicraeosauridae)". Historical Biology. 36 (7): 1343–1367. doi:10.1080/08912963.2023.2212389. S2CID 258965010.
- ^ Wedel, M. J.; Taylor, M. P. (2023). "The biomechanical significance of bifurcated cervical ribs in apatosaurine sauropods". Vertebrate Anatomy Morphology Palaeontology. 11: 91–100. doi:10.18435/vamp29394.
- ^ Lerzo, Lucas N. (2023). "Redescription of the key specimen MACN PV 35: Laminar anatomy and hyposphene-hypantrum in an early rebbachisaurid (Dinosauria, Sauropoda) from Patagonia, Argentina". Cretaceous Research. 153: 105689. doi:10.1016/j.cretres.2023.105689. S2CID 261407536.
- ^ Lefebvre, R.; Allain, R.; Houssaye, A. (2023). "What's inside a sauropod limb? First three-dimensional investigation of the limb long bone microanatomy of a sauropod dinosaur, Nigersaurus taqueti (Neosauropoda, Rebbachisauridae), and implications for the weight-bearing function". Palaeontology. 66 (4). e12670. Bibcode:2023Palgy..6612670L. doi:10.1111/pala.12670. S2CID 260415756.
- ^ Bellardini, F.; Filippi, L. S.; Carballido, J. L.; Garrido, A. C.; Baiano, M. A. (2023). "Exploring rebbachisaurid hind-limb anatomy on the basis of a new articulated specimen from the Huincul Formation (upper Cenomanian) of Neuquén Basin, Patagonia, Argentina". Historical Biology: 1–17. doi:10.1080/08912963.2023.2268638. S2CID 264505293.
- ^ Torcida Fernández-Baldor, F.; Huerta, P.; Puértolas-Pascual, E.; Canudo, J. I. (2023). "New teeth of a basal Macronarian (Sauropoda) from the Jurassic–Cretaceous transition of Spain". Journal of Iberian Geology. 50: 27–39. doi:10.1007/s41513-023-00217-7. S2CID 261795642.
- ^ Tatehata, J.-I.; Mukunoki, T.; Tanoue, K. (2023). "Description of a Titanosauriform (Sauropoda, Dinosauria) Cervical Vertebra from the Lower Cretaceous Kanmon Group, Southwestern Japan". Paleontological Research. 27 (3): 350–358. doi:10.2517/PR220009. S2CID 255441172.
- ^ Hornung, J. J.; Sachs, S.; Schwermann, A. H. (2023). "The first record of sauropod dinosaurs from a palaeotopographical upland environment and its implications for megaherbivorous dinosaur faunal turnover in the Early Cretaceous of northwestern Europe". Geologie und Paläontologie in Westfalen. 97: 3–36.
- ^ Taylor, M. P.; Wedel, M. J. (2023). "Novel pneumatic features in the ribs of the sauropod dinosaur Brachiosaurus altithorax". Acta Palaeontologica Polonica. 68 (4): 709–718. doi:10.4202/app.01105.2023.
- ^ Lim, V.; Buffetaut, E.; Tong, H.; Cavin, L.; Pann, K.; Ngoeun, P. P. (2023). "The First Dinosaur from the Kingdom of Cambodia: A Sauropod Fibula from the Lower Cretaceous of Koh Kong Province, South-Western Cambodia". Fossils. 1 (1): 49–59. doi:10.3390/fossils1010006.
- ^ Cruzado-Caballero, P; Fillipi, L.S.; Gonzalez-Dionis, J; Canudo, JI (2023-03-21). "How Common Are Lesions on the Tails of Sauropods? Two New Pathologies in Titanosaurs from the Late Cretaceous of Argentine Patagonia". Diversity. 15 (3): 464. doi:10.3390/d15030464.
- ^ Fronimos, John A (2023-10-11). "Patterns and function of pneumaticity in the vertebrae, ribs, and ilium of a titanosaur (Dinosauria, Sauropoda) from the Upper Cretaceous of Texas". Journal of Vertebrate Paleontology. 43 (2). e2259444. doi:10.1080/02724634.2023.2259444. S2CID 266964996.
- ^ Averianov, A.; Podlesnov, A.; Slobodin, D.; Skutschas, P.; Feofanova, O.; Vladimirova, O. (2023). "First sauropod dinosaur remains from the Early Cretaceous Shestakovo 3 locality, Western Siberia, Russia". Biological Communications. 68 (4): 236–252. doi:10.21638/spbu03.2023.404. S2CID 267453019.
- ^ Poropat, S. F.; Mannion, P. D.; Rigby, S. L.; Duncan, R. J.; Pentland, A. H.; Bevitt, J. J.; Sloan, T.; Elliott, D. A. (2023). "A nearly complete skull of the sauropod dinosaur Diamantinasaurus matildae from the Upper Cretaceous Winton Formation of Australia and implications for the early evolution of titanosaurs". Royal Society Open Science. 10 (4). 221618. Bibcode:2023RSOS...1021618P. doi:10.1098/rsos.221618. PMC 10090887. PMID 37063988.
- ^ Silva Junior, J. C. G.; Marinho, T. S.; Martinelli, A. G.; Ribeiro, L. C. B.; Langer, M. C. (2023). "The largest known titanosaur (Dinosauria, Sauropoda) tooth and other isolated dental elements from the Serra da Galga Formation (Cretaceous of Southeast Brazil)". Cretaceous Research. 105656. doi:10.1016/j.cretres.2023.105656. S2CID 259942879.
- ^ Dhiman, H.; Verma, V.; Singh, L. R.; Miglani, V.; Jha, D. K.; Sanyal, P.; Tandon, S. K.; Prasad, G. V. R. (2023). "New Late Cretaceous titanosaur sauropod dinosaur egg clutches from lower Narmada valley, India: Palaeobiology and taphonomy". PLOS ONE. 18 (1). e0278242. Bibcode:2023PLoSO..1878242D. doi:10.1371/journal.pone.0278242. PMC 9848018. PMID 36652404.
- ^ Windholz, G. J.; González, R.; Cerda, I. A.; Bellardini, F.; Silva, J. C. G.; Marinho, T. S.; Ribeiro, L. C. B.; Martinelli, A. G. (2023). "Osteohistology of Uberabatitan ribeiroi (Dinosauria, Sauropoda) provides insight into the life history of titanosaurs". Historical Biology: 1–11. doi:10.1080/08912963.2023.2253257. S2CID 261626549.
- ^ González, R.; Cerda, I. A.; Pérez Moreno, A.; Calvo, J. O.; González Riga, B. J. (2023). "Paleobiology of Rinconsaurus caudamirus and Muyelensaurus pecheni (Sauropoda, Titanosauria) from the Neuquén Group, Upper Cretaceous of Argentina: inferences from long bone histology". Cretaceous Research. 153. 105682. doi:10.1016/j.cretres.2023.105682. S2CID 261671535.
- ^ Wahba, D. G. A.; Abu El-Kheir, G. A.; Tantawy, A. A.; AbdelGawad, M. (2023). "A new record of saltasaurids in Africa; new evidence from the Middle Campanian, Western Desert, Egypt". Historical Biology: 1–5. doi:10.1080/08912963.2023.2252445. S2CID 261551929.
- ^ Averianov, A.O.; Bolotsky, YL; Bolotsky, YI (2023-03-14). "A Sauropod from the Late Cretaceous of the Amur Region". Doklady Earth Sciences. 507: S418–S419. doi:10.1134/S1028334X22601547. S2CID 257498576.
- ^ Paul, Gregory S.; Larramendi, Asier (2023-04-11). "Body mass estimate of Bruhathkayosaurus and other fragmentary sauropod remains suggest the largest land animals were about as big as the greatest whales". Lethaia. 56 (2): 1–11. Bibcode:2023Letha..56..2.5P. doi:10.18261/let.56.2.5. ISSN 0024-1164. S2CID 259782734.
- ^ Zaagane, M.; Hunt, A. P.; Bendella, M.; Lucas, S. G.; Draoui, A.; Mouzti, O. (2023). "Multiple trackways from the Cenomanian Djoua series, in In Amenas region (southeastern Algeria), represent the first ichnological evidence of gregarious behavior in Cretaceous sauropods from Africa". Historical Biology: 1–13. doi:10.1080/08912963.2023.2269173. S2CID 265199614.
- ^ Button, D. J.; Porro, L. B.; Lautenschlager, S.; Jones, M. E. H.; Barrett, P. M. (2023). "Multiple pathways to herbivory underpinned deep divergences in ornithischian evolution". Current Biology. 33 (3): 557–565.e7. Bibcode:2023CBio...33E.557B. doi:10.1016/j.cub.2022.12.019. PMID 36603586.
- ^ Dempsey, M.; Maidment, S. C. R.; Hedrick, B. P.; Bates, K. T. (2023). "Convergent evolution of quadrupedality in ornithischian dinosaurs was achieved through disparate forelimb muscle mechanics". Proceedings of the Royal Society B: Biological Sciences. 290 (1992). 20222435. doi:10.1098/rspb.2022.2435. PMC 9890092. PMID 36722082. S2CID 256416920.
- ^ Manitkoon, S.; Deesri, U.; Warapeang, P.; Nonsrirach, T.; Chanthasit, P. (2023). "Ornithischian dinosaurs in Southeast Asia: a review with palaeobiogeographic implications". Fossil Record. 26 (1): 1–25. Bibcode:2023FossR..26....1M. doi:10.3897/fr.26.e93456. S2CID 255661505.
- ^ Surmik, D.; Słowiak-Morkovina, J.; Szczygielski, T.; Wojtyniak, M.; Środek, D.; Dulski, M.; Balin, K.; Krzykawski, T.; Pawlicki, R. (2023). "The first record of fossilized soft parts in ossified tendons and implications for the understanding of tendon mineralization". Zoological Journal of the Linnean Society. 198 (3): 747–766. doi:10.1093/zoolinnean/zlad001.
- ^ Calvert, C. E.; Hunt, T. C.; Whalen, N. S.; Choiniere, J. N.; Norell, M. A.; Erickson, G. M (2023). "Enamel microstructure and dental histology in a heterodontosaurid dinosaur: Heterodontosaurus tucki". Acta Palaeontologica Polonica. 68 (4): 603–612. doi:10.4202/app.01060.2023.
- ^ Becerra, M. G.; Pol, D.; Porro, L. B.; Paulina-Carabajal, A.; Rauhut, O. W. M. (2023). "Craniomandibular osteology of Manidens condorensis (Ornithischia: Heterodontosauridae) from the upper Lower Jurassic of Argentina". Journal of Vertebrate Paleontology. 42 (3). e2181087. doi:10.1080/02724634.2023.2181087. S2CID 257944241.
- ^ Button, D. J.; Zanno, L. E. (2023). "Neuroanatomy of the late Cretaceous Thescelosaurus neglectus (Neornithischia: Thescelosauridae) reveals novel ecological specialisations within Dinosauria". Scientific Reports. 13 (1). 19224. Bibcode:2023NatSR..1319224B. doi:10.1038/s41598-023-45658-3. PMC 10628235. PMID 37932280.
- ^ Raven, T. J.; Barrett, P. M.; Joyce, C. B.; Maidment, S. C. R. (2023). "The phylogenetic relationships and evolutionary history of the armoured dinosaurs (Ornithischia: Thyreophora)" (PDF). Journal of Systematic Palaeontology. 21 (1). 2205433. Bibcode:2023JSPal..2105433R. doi:10.1080/14772019.2023.2205433. S2CID 258802937.
- ^ Anderson, L; Brassey, C; Pod, S; Bates, K; Sellers, W.I. (2023-03-10). "Investigating the quadrupedal abilities of Scutellosaurus lawleri and its implications for locomotor behavior evolution among dinosaurs". The Anatomical Record. 306 (10): 2514–2536. doi:10.1002/ar.25189. PMID 36896818. S2CID 257428246.
- ^ Gilmore, C. W. (1914). "Osteology of the armored Dinosauria in the United States National Museum, with special reference to the genus Stegosaurus". Bulletin of the United States National Museum. 89: 1–143. hdl:10088/30429.
- ^ Galton, P. M. (2023). "A sternal bone of plated ornithischian dinosaur Stegosaurus (Upper Jurassic, Utah), the first for Stegosauria, and the enigmatic "sternal bones" of Gilmore (1914)". Revue de Paléobiologie, Genève. 42 (1): 129–141. doi:10.5281/zenodo.7446065.
- ^ Brum, Arthur S.; Eleutério, Lúcia; Simōes, Tiago; Whitney, Megan; Souza, Geovane; Sayāo, Juliana; Kellner, Alexander (2023-02-20). "Ankylosaurian body armor function and evolution with insights from osteohistology and morphometrics of new specimens from the Late Cretaceous of Antarctica". Paleobiology. 49 (4): 579–600. Bibcode:2023Pbio...49..579B. doi:10.1017/pab.2023.4. S2CID 257073096.
- ^ Yoshida, J.; Kobayashi, Y.; Norell, M. A. (2023). "An ankylosaur larynx provides insights for bird-like vocalization in non-avian dinosaurs". Communications Biology. 6 (1). 152. doi:10.1038/s42003-023-04513-x. PMC 9932143. PMID 36792659.
- ^ Tumanova, T.; Penkalski, P.; Gallagher, W. B.; Engiles, J. B.; Dodson, P. (2023). "A potentially fatal cranial pathology in a specimen of Tarchia". The Anatomical Record. doi:10.1002/ar.25205. PMID 37014144. S2CID 257922988.
- ^ Ballell, A.; Mai, B.; Benton, M. J. (2023). "Divergent strategies in cranial biomechanics and feeding ecology of the ankylosaurian dinosaurs". Scientific Reports. 13 (1). 18242. Bibcode:2023NatSR..1318242B. doi:10.1038/s41598-023-45444-1. PMC 10600113. PMID 37880323.
- ^ Kubo, T.; Kubo, M. O.; Sakamoto, M.; Winkler, D. E.; Shibata, M.; Zheng, W.; Jin, X.; You, H.-L. (2023). "Dental microwear texture analysis reveals a likely dietary shift within Late Cretaceous ornithopod dinosaurs". Palaeontology. 66 (6). e12681. Bibcode:2023Palgy..6612681K. doi:10.1111/pala.12681. S2CID 265604383.
- ^ Augustin, F. J.; Ősi, A.; Csiki-Sava, Z. (2023). "The Rhabdodontidae (Dinosauria, Ornithischia), an enigmatic dinosaur group endemic to the Late Cretaceous European Archipelago". Fossil Record. 26 (2): 171–189. doi:10.3897/fr.26.108967.
- ^ Magyar, J.; Csiki-Sava, Z.; Ősi, A.; Augustin, F. J.; Botfalvai, G. (2023). "Rhabdodontid (Dinosauria, Ornithopoda) diversity suggested by the first documented occurrence of associated cranial and postcranial material at Vălioara (uppermost Cretaceous Densuș-Ciula Formation, Hațeg Basin, Romania)". Cretaceous Research. 156. 105810. doi:10.1016/j.cretres.2023.105810. S2CID 266414358.
- ^ Maidment, S. C. R.; Chapelle, K. E. J.; Bonsor, J. A.; Button, D.; Barrett, P. M. (2023). "Osteology and relationships of Cumnoria prestwichii (Ornithischia: Ornithopoda) from the Late Jurassic of Oxfordshire, UK". Monographs of the Palaeontographical Society. 176 (664): 1–55. doi:10.1080/02693445.2022.2162669. S2CID 256107302.
- ^ Rotatori, F. M.; Quaranta, M.; Bertozzo, F.; Hübner, T.; Camilo, B.; Mateus, O.; Moreno-Azanza, M. (2023). "Hadrosaur-like vascularisation in the dentary of an early diverging iguanodontian dinosaur". Historical Biology: 1–6. doi:10.1080/08912963.2023.2238727. S2CID 260143876.
- ^ Bonsor, J. A.; Lockwood, J. A. F.; Leite, J. V.; Scott-Murray, A.; Maidment, S. C. R. (2023). "The osteology of the holotype of the British iguanodontian dinosaur Mantellisaurus atherfieldensis". Monographs of the Palaeontographical Society. 177 (665): 1–63. Bibcode:2023MPalS.177....1B. doi:10.1080/02693445.2023.2234156. S2CID 259985730.
- ^ García-Cobeña, J.; Cobosa, A.; Verdú, F. J. (2023). "Ornithopod tracks and bones: Paleoecology and an unusual evidence of quadrupedal locomotion in the Lower Cretaceous of eastern Iberia (Teruel, Spain)". Cretaceous Research. 144. 105473. Bibcode:2023CrRes.14405473G. doi:10.1016/j.cretres.2023.105473. S2CID 255679510.
- ^ Rodríguez-Barreiro, I.; Santos, A. A.; Villanueva-Amadoz, U.; Gasulla, J. M.; Escaso, F.; Ortega, F.; Gee, C. T.; Diez, J. B. (2023). "Palynological reconstruction of the habitat and diet of Iguanodon bernissartensis in the Lower Cretaceous Morella Formation, NE Iberian Peninsula". Cretaceous Research. 156. 105804. doi:10.1016/j.cretres.2023.105804. hdl:11093/6370.
- ^ Söderblom, D. F. K.; Blanco, A.; Prieto-Márquez, A.; Campione, N. E. (2023). "The dentary of hadrosauroid dinosaurs: evolution through heterochrony". Palaeontology. 66 (5). e12674. Bibcode:2023Palgy..6612674S. doi:10.1111/pala.12674.
- ^ Bapinaev, R. A.; Golovneva, L. B.; Zolina, A. A.; Averianov, A. A.; Skutschas, P. P. (2023). "New data on high-latitude hadrosaurid dinosaurs from the Upper Cretaceous Kakanaut Formation of Chukotka, Russia". Cretaceous Research. 149. 105552. Bibcode:2023CrRes.14905552B. doi:10.1016/j.cretres.2023.105552. S2CID 258091135.
- ^ Joubarne, T.; Therrien, F.; Zelenitsky, D. (2023). "Integumentary impressions on hadrosaurid specimens from the Upper Cretaceous (upper Campanian) Dinosaur Park Formation, Alberta, Canada: implications for integument patterns and hand morphology". Journal of Vertebrate Paleontology. 42 (6). e2213287. doi:10.1080/02724634.2023.2213287. S2CID 259402283.
- ^ Dudgeon, T.W.; Evans, D.C. (2023-03-10). "Calvarial suture interdigitation in hadrosaurids (Ornithischia: Ornithopoda): Perspectives through ontogeny and evolution". Evolution & Development. 25 (3): 209–225. doi:10.1111/ede.12430. PMID 36896717. S2CID 257428248.
- ^ Currie, P. J.; Lü, J.; Wang, Y.Y. (2023). "A juvenile hadrosaur maxilla from the Dinosaur Park Formation (Campanian) of Dinosaur Provincial Park (Alberta, Canada)". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 166–175. ISBN 978-89-5708-358-1.
- ^ Zhang, J.; Wang, X.; Jiang, S.; Li, G. (2023). "The postcranial anatomy of the saurolophine hadrosaurid Laiyangosaurus youngi from the Upper Cretaceous of Laiyang, Shandong, China". The Anatomical Record. doi:10.1002/ar.25291. PMID 37466167. S2CID 259974467.
- ^ Seymour, R. S.; Seymour, H. R.; Woodward, H. N.; Hu, Q. (2023). "Growth rate affects blood flow rate to the tibia of the dinosaur Maiasaura". Paleobiology. 50: 123–129. doi:10.1017/pab.2023.24. hdl:2440/140689. S2CID 261853463.
- ^ Dyer, A. D.; Powers, M. J.; Currie, P. J. (2023). "Problematic putative pachycephalosaurids: synchrotron μCT imaging shines new light on the anatomy and taxonomic validity of Gravitholus albertae from the Belly River Group (Campanian) of Alberta, Canada". Vertebrate Anatomy Morphology Palaeontology. 10 (1): 65–110. doi:10.18435/vamp29388. S2CID 257046495.
- ^ Han, G.; Mallon, J. C.; Lussier, A. J.; Wu, X.-C.; Mitchell, R.; Li, L.-J. (2023). "An extraordinary fossil captures the struggle for existence during the Mesozoic". Scientific Reports. 13 (1). 11221. Bibcode:2023NatSR..1311221H. doi:10.1038/s41598-023-37545-8. PMC 10354204. PMID 37464026.
- ^ Yang, Y.; Gong, E.; Zhao, C.; Wu, W.; Godefroit, P.; Hu, D. (2023). "Endocranial morphology of Liaoceratops yanzigouensis (Dinosauria: Ceratopsia) from Early Cretaceous Jehol Biota of Liaoning in China". Historical Biology. 36 (3): 650–656. doi:10.1080/08912963.2023.2180739. S2CID 257227953.
- ^ Nabavizadeh, A (2023-03-08). "How Triceratops got its face: An update on the functional evolution of the ceratopsian head". The Anatomical Record. 306 (7): 1951–1968. doi:10.1002/ar.25196. PMID 36883781. S2CID 257404473.
- ^ Chiba, K.; Ryan, M. J.; Saneyoshi, M.; Konishi, S.; Yamamoto, Y.; Evans, D. C.; Chinzorig, T.; Khatanbaatar, P.; Badamkhatan, Z.; Mainbayar, B.; Tsogtbaatar, K. (2023). "New insights on the frill ornamentations of protoceratopsids". In Yuong-Nam Lee (ed.). Windows into sauropsid and synapsid evolution. Essays in honor of Louis L. Jacobs. Dinosaur Science Center Press. pp. 140–150. ISBN 978-89-5708-358-1.
- ^ Berry, K. (2023). "Q: How could western North America support such a high diversity of ecologically similar, large-bodied horned dinosaur species during the late Campanian? A: It could not - or, the Red Queen takes an axe to a phylogenetic tree, restructuring an ecological network from within rather than without". New Mexico Museum of Natural History and Science Bulletin. 94: 65–78.
- ^ Mallon, Jordan C.; Holmes, Robert B.; Rufolo, Scott J. (2023-06-13). "Development and homology of the medial parietal ornamentation in centrosaurine ceratopsids (Dinosauria, Ornithischia)". Journal of Vertebrate Paleontology. 42 (5). doi:10.1080/02724634.2023.2211637. ISSN 0272-4634. S2CID 259335390.
- ^ de Rooij, J.; Lucassen, S. A. N.; Furer, C.; Schulp, A. S.; Sander, P. M. (2023). "Exploring the ceratopsid growth record: a comprehensive osteohistological analysis of Triceratops (Ornithischia: Ceratopsidae) and its implications for growth and ontogeny". Cretaceous Research. 154. 105738. doi:10.1016/j.cretres.2023.105738.
- ^ Senter, P. J.; Mackey, J. J. (2023). "Forelimb motion and orientation in the ornithischian dinosaurs Styracosaurus and Thescelosaurus, and its implications for locomotion and other behavior". Palaeontologia Electronica. 26 (3). 26.3.a41. doi:10.26879/1289.
- ^ a b Houde, Peter; Dickson, Meig; Camarena, Dakota (2023). "Basal Anseriformes from the Early Paleogene of North America and Europe". Diversity. 7 (2): 233. doi:10.3390/d15020233.
- ^ a b c Mayr, G.; Kitchener, A. C. (2023). "The Vastanavidae and Messelasturidae (Aves) from the early Eocene London Clay of Walton-on-the-Naze (Essex, UK)". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 307 (2): 113–139. doi:10.1127/njgpa/2023/1119. S2CID 257598310.
- ^ a b Zelenkov, N. V. (2023). "Small ducks (Aves: Anatidae) from the early-middle Miocene of Eurasia. 3. A revision of Mionetta natator (Milne-Edwards, 1867)". Paleontological Journal. 57 (6): 659–670. Bibcode:2023PalJ...57..659Z. doi:10.1134/S0031030123060114. S2CID 265501250.
- ^ Buffetaut, E.; Angst, D.; Tong, H. (2023). "A new enantiornithine bird from Upper Cretaceous non-marine deposits at Villespassans (Hérault, southern France)". Annales de Paléontologie. 109 (1). 102585. Bibcode:2023AnPal.10902585B. doi:10.1016/j.annpal.2022.102585. S2CID 257863645.
- ^ Mayr, G.; Kitchener, A. C. (2023). "Early Eocene fossils elucidate the evolutionary history of the Charadriiformes (shorebirds and allies)". Journal of Paleontology. 97 (4): 941–955. Bibcode:2023JPal...97..941M. doi:10.1017/jpa.2023.51. S2CID 262192324.
- ^ Mayr, G.; De Pietri, V. L.; Love, L.; Mannering, A.; Crouch, E.; Reid, C.; Scofield, R. P. (2023). "Partial skeleton from the Paleocene of New Zealand illuminates the early evolutionary history of the Phaethontiformes (tropicbirds)". Alcheringa: An Australasian Journal of Palaeontology. 47 (3): 315–326. Bibcode:2023Alch...47..315M. doi:10.1080/03115518.2023.2246528. S2CID 261376790.
- ^ Li, Z; Wang, M.; Stidham, T. A.; Zhou, Z. (2023). "Decoupling the skull and skeleton in a Cretaceous bird with unique appendicular morphologies". Nature Ecology & Evolution. 7 (1): 20–31. Bibcode:2023NatEE...7...20L. doi:10.1038/s41559-022-01921-w. PMID 36593291. S2CID 255472056.
- ^ a b Mayr, G.; Carrió, V.; Kitchener, A. C. (2023). "On the "screamer-like" birds from the British London Clay: An archaic anseriform-galliform mosaic and a non-galloanserine "barb-necked" species of Perplexicervix". Palaeontologia Electronica. 26 (2). 26.2.a33. doi:10.26879/1301.
- ^ Mather, Ellen K.; Lee, Michael S. Y.; Camens, Aaron B.; Worthy, Trevor H. (2023-03-15). "A giant raptor (Aves: Accipitridae) from the Pleistocene of southern Australia". Journal of Ornithology. 164 (3): 499–526. doi:10.1007/s10336-023-02055-x. ISSN 2193-7192. S2CID 257575533.
- ^ Mather, Ellen K.; Lee, Michael S. Y.; Fusco, Diana A.; Hellstrom, John; Worthy, Trevor H. (2023-11-19). "Pleistocene raptors from cave deposits of South Australia, with a description of a new species of Dynatoaetus (Accipitridae: Aves): morphology, systematics and palaeoecological implications". Alcheringa: An Australasian Journal of Palaeontology. 48: 134–167. doi:10.1080/03115518.2023.2268780. ISSN 0311-5518.
- ^ Mayr, G.; De Pietri, V. L.; Kitchener, A. C. (2023). "Narrow-beaked trogons from the early Eocene London Clay of Walton-on-the-Naze (Essex, UK)". Journal of Ornithology. 164 (4): 749–764. doi:10.1007/s10336-023-02071-x. S2CID 258545691.
- ^ Thomas, D. B.; Tennyson, A. J. D.; Marx, F. G.; Ksepka, D. T. (2023). "Pliocene fossils support a New Zealand origin for the smallest extant penguins". Journal of Paleontology. 97 (3): 711–721. Bibcode:2023JPal...97..711T. doi:10.1017/jpa.2023.30. S2CID 259778756.
- ^ Emslie, S. D.; Mead, J. I. (2023). "Two New Late Quaternary Avifaunas from the East-Central Great Basin with the Description of a New Species of Falco". Western North American Naturalist. 83 (1): 33–50. doi:10.3398/064.083.0104. S2CID 260499492.
- ^ Xu, Liming; Wang, Min; Chen, Runsheng; Dong, Liping; Lin, Min; Xu, Xing; Tang, Jianrong; You, Hailu; Zhou, Guowu; Wang, Linchang; He, Wenxing; Li, Yujuan; Zhang, Chi; Zhou, Zhonghe (2023-09-06). "A new avialan theropod from an emerging Jurassic terrestrial fauna". Nature. 621 (7978): 336–343. Bibcode:2023Natur.621..336X. doi:10.1038/s41586-023-06513-7. ISSN 1476-4687. PMID 37674081. S2CID 261581753.
- ^ a b Ksepka, D. T.; Field, D. J.; Heath, T. A.; Pett, W.; Thomas, D. B.; Giovanardi, S.; Tennyson, A. J. D. (2023). "Largest-known fossil penguin provides insight into the early evolution of sphenisciform body size and flipper anatomy". Journal of Paleontology. 97 (2): 434–453. Bibcode:2023JPal...97..434K. doi:10.1017/jpa.2022.88. S2CID 256709376.
- ^ Bocheński, Z. M.; Happ, J.; Salwa, G.; Tomek, T. (2023). "An intriguing new species of dabbling duck (Aves: Anseriformes) from the middle Miocene of Austria". Palaeontologia Electronica. 26 (3). 26.3.a52. doi:10.26879/1334.
- ^ Tennyson, A.J.D.; Salvador, R.B. (2023). "A New Giant Petrel (Macronectes, Aves: Procellariidae) from the Pliocene of Taranaki, New Zealand". Taxonomy. 3 (1): 57–67. doi:10.3390/taxonomy3010006. hdl:10037/29075.
- ^ a b c Zelenkov, N. V. (2023). "Small ducks (Aves: Anatidae) from the early-middle Miocene of Eurasia. Part 2. The fauna of Tagay locality (Baikal Region; eastern Siberia)". Paleontological Journal. 57 (5): 560–572. Bibcode:2023PalJ...57..560Z. doi:10.1134/S003103012305012X. S2CID 262549607.
- ^ Worthy, Trevor H.; De Pietri, Vanesa L.; Scofield, R. Paul; Hand, Suzanne J. (2023-03-20). "A new Eocene species of presbyornithid (Aves, Anseriformes) from Murgon, Australia". Alcheringa: An Australasian Journal of Palaeontology. 47 (4): 416–430. Bibcode:2023Alch...47..416W. doi:10.1080/03115518.2023.2184491. ISSN 0311-5518. S2CID 257679005.
- ^ Hume, J. P. (2023). "A new fossil subspecies of booby (Aves, Sulidae: Papasula) from Mauritius and Rodrigues, Mascarene Islands, with notes on P. abbotti from Assumption Island". Zootaxa. 5270 (3): 507–536. doi:10.11646/zootaxa.5270.3.5. PMID 37518153. S2CID 258282986.
- ^ a b Mourer-Chauviré, C.; Bourdon, E.; Duffaud, S.; Le Roux, G.; Laurent, Y. (2023). "New avian remains from the early Eocene of La Borie, southern France". Geobios. 83: 61–84. doi:10.1016/j.geobios.2022.10.004. S2CID 257251285.
- ^ Noriega, Jorge I.; Cenizo, Marcos; Brandoni, Diego; Pérez, Leandro M.; Tineo, David E.; Diederle, Juan M.; Bona, Paula (2023-05-09). "A new pelican (Aves: Pelecanidae) from the Upper Miocene of Argentina: new clues about the origin of the New World lineages". Journal of Vertebrate Paleontology. 42 (5): e2202702. doi:10.1080/02724634.2023.2202702. ISSN 0272-4634. S2CID 258605013.
- ^ Ksepka, D. T.; Tennyson, A. J. D.; Richards, M. D.; Fordyce, R. E. (2023). "Stem albatrosses wandered far: a new species of Plotornis (Aves, Pan-Diomedeidae) from the earliest Miocene of New Zealand". Journal of the Royal Society of New Zealand. 54 (5): 643–659. doi:10.1080/03036758.2023.2266390. PMC 11459804.
- ^ a b c Zelenkov, Nikita; Palastrova, Ekaterina; Martynovich, Nikolay; Klementiev, Alexey; Sizov, Alexander; Volkova, Natalia (2023-12-31). "A tiny duck (Sibirionetta formozovi sp. nov.), a giant grey partridge (Titanoperdix felixi gen. et sp. nov.), a new rail (Porzana payevskyi sp. nov.), and other birds from the Early Pleistocene of Baikalian Siberia". Biological Communications. 68 (4): 261–272. doi:10.21638/spbu03.2023.406. ISSN 2587-5779.
- ^ Kessler, J.; Horváth, I. (2023). "Praecarbo strigoniensis, a new genus and species of Cormorants (Phalacrocoracinae) from the Late Oligocene of Hungary". Ornis Hungarica. 31 (1): 126–132. doi:10.2478/orhu-2023-0008. S2CID 259119955.
- ^ Zelenkov, N.V. (2023). "A new species of sandgrouse (Aves: Pteroclidae) from the early Pleistocene of the Crimea". Doklady Biological Sciences. 511 (1): 264–266. doi:10.1134/S0012496623700497. PMID 37833584. S2CID 264040045.
- ^ a b Mayr, G.; Kitchener, A. C. (2023). "The Halcyornithidae from the early Eocene London Clay of Walton-on-the-Naze (Essex, UK): A species complex of Paleogene arboreal birds". Geobios. 83: 45–60. doi:10.1016/j.geobios.2023.06.003. S2CID 259969084.
- ^ Mayr, G.; Kitchener, A. C. (2023). "Multiple skeletons of Rhynchaeites from the London Clay reveal the osteology of early Eocene ibises (Aves, Threskiornithidae)". PalZ. 97 (2): 425–442. Bibcode:2023PalZ...97..425M. doi:10.1007/s12542-022-00647-1. S2CID 256163083.
- ^ Nguyen, J. M. T. (2023). "The earliest record of bowerbirds (Passeriformes, Ptilonorhynchidae) from the Oligo-Miocene of northern Australia". Alcheringa: An Australasian Journal of Palaeontology. 47 (4): 475–483. Bibcode:2023Alch...47..475N. doi:10.1080/03115518.2023.2180537. S2CID 257578512.
- ^ Mayr, Gerald; Kitchener, Andrew (2023). "A new fossil from the London Clay documents the convergent origin of a "mousebird-like" tarsometatarsus in an early Eocene near-passerine bird". Acta Palaeontologica Polonica. 68 (1): 1–11. doi:10.4202/app.01049.2022. S2CID 257422961.
- ^ Agnolín, Federico L. (2023). "A new species of the Falcon genus Thegornis (Aves) from the Miocene of Northwestern Argentina" (PDF). Historia Natural. 13 (2): 15–24.
- ^ Degrange, F. J.; Bonini, R. A.; Georgieff, S. M.; Ibañez, L. M. (2023). "A new fossil condor (Aves, Cathartiformes) from the Early Pliocene of Catamarca province, Argentina". Historical Biology: An International Journal of Paleobiology: 1–6. doi:10.1080/08912963.2023.2288612. S2CID 266076044.
- ^ Tambussi, Claudia P.; Degrange, Federico J.; González Ruiz, Laureano (2023-03-06). "An extinct owl (aves: strigidae) from the middle miocene of Patagonia". Historical Biology. 36 (3): 644–649. doi:10.1080/08912963.2023.2180738. ISSN 0891-2963. S2CID 257392373.
- ^ Mayr, G.; Kitchener, A. C. (2022). "Early Eocene fossil illuminates the ancestral (diurnal) ecomorphology of owls and documents a mosaic evolution of the strigiform body plan". Ibis. 165 (1): 231–247. doi:10.1111/ibi.13125. S2CID 251455832.
- ^ Wang, M.; Zhou, Z. (2023). "Low morphological disparity and decelerated rate of limb size evolution close to the origin of birds". Nature Ecology & Evolution. 7 (8): 1257–1266. Bibcode:2023NatEE...7.1257W. doi:10.1038/s41559-023-02091-z. PMID 37277496. S2CID 259090599.
- ^ Macaulay, S.; Hoehfurtner, T.; Cross, S. R. R.; Marek, R. D.; Hutchinson, J. R.; Schachner, E. R.; Maher, A. E.; Bates, K. T. (2023). "Decoupling body shape and mass distribution in birds and their dinosaurian ancestors". Nature Communications. 14 (1). 1575. Bibcode:2023NatCo..14.1575M. doi:10.1038/s41467-023-37317-y. PMC 10033513. PMID 36949094.
- ^ Wang, Y.; Li, Z.; Wang, C.-C.; Bailleul, A. M.; Wang, M.; O'Connor, J.; Li, J.; Zheng, X.; Pei, R.; Teng, F.; Wang, X.; Zhou, Z. (2023). "Comparative microstructural study on the teeth of Mesozoic birds and non-avian dinosaurs". Royal Society Open Science. 10 (5). 230147. Bibcode:2023RSOS...1030147W. doi:10.1098/rsos.230147. PMC 10189602. PMID 37206961.
- ^ Kiat, Y.; O'Connor, J. K. (2023). "Rarity of molt evidence in early pennaraptoran dinosaurs suggests annual molt evolved later among Neornithes". Communications Biology. 6 (1). 687. doi:10.1038/s42003-023-05048-x. PMC 10317961. PMID 37400509.
- ^ Hong, S.-Y.; Lee, Y.-N.; Kong, D.-Y.; Jung, S.-H. (2023). "The discovery of Wupus agilis in South Korea and a new quantitative analysis of intermediate ichnospecies between non-avian theropods and birds". Cretaceous Research. 155. 105785. doi:10.1016/j.cretres.2023.105785. S2CID 265453414.
- ^ Martin, A. J.; Lowery, M.; Hall, M.; Vickers-Rich, P.; Rich, T. H.; Serrano-Brañas, C. I.; Swinkels, P. (2023). "Earliest known Gondwanan bird tracks: Wonthaggi Formation (Early Cretaceous), Victoria, Australia". PLOS ONE. 18 (11). e0293308. Bibcode:2023PLoSO..1893308M. doi:10.1371/journal.pone.0293308. PMC 10651008. PMID 37967053.
- ^ Wu, Y.; Ge, Y.; Hu, H.; Stidham, T. A.; Li, Z.; Bailleul, A. M.; Zhou, Z. (2023). "Intra-gastric phytoliths provide evidence for folivory in basal avialans of the Early Cretaceous Jehol Biota". Nature Communications. 14 (1). 4558. Bibcode:2023NatCo..14.4558W. doi:10.1038/s41467-023-40311-z. PMC 10382595. PMID 37507397.
- ^ Zhao, Yan; Tian, Qian; Ren, Guang-Ying; Guo, Ying; Zheng, Xiao-Ting (2023). "Taphonomic analysis of the exceptional preservation of early bird feathers during the early Cretaceous period in Northeast China". Frontiers in Earth Science. 10. Bibcode:2023FrEaS..1020594Z. doi:10.3389/feart.2022.1020594.
- ^ Chiappe, L. M.; Serrano, F. J.; Abramowicz, S.; Göhlich, U. B. (2023). "Flight performance of the Early Cretaceous bird Confuciusornis sanctus: evidence from an exceptionally preserved fossil". Spanish Journal of Palaeontology. 38 (2): 101–122. doi:10.7203/sjp.27543.
- ^ Nebreda, Sergio M.; Chiappe, Luis M.; Navalon, Guillermo; Chinsamy, Anusuya; Sanz, José L.; Buscalioni, Angela D.; Marugán-Lobón, Jesús (2023). "A new enantiornithine specimen from the Lower Cretaceous of Las Hoyas: avifaunal diversity and life-history of a wetland Mesozoic bird". Spanish Journal of Palaeontology. 38 (2): 123–136. doi:10.7203/sjp.26504. hdl:10486/713215. S2CID 258658656.
- ^ O'Connor, J.; Kiat, Y.; Ma, H.; Ai, T.; Wang, L.; Bi, S. (2023). "Immature feathers preserved in Burmite provide evidence of rapid molting in enantiornithines". Cretaceous Research. 149. 105572. Bibcode:2023CrRes.14905572O. doi:10.1016/j.cretres.2023.105572. S2CID 258543838.
- ^ Wang, S.; Li, L.; Zhao, C.; Rummy, P.; Wang, R.; Hu, D. (2023). "Redescription and phylogenetic affinities of the Early Cretaceous enantiornithine Dapingfangornis sentisorhinus". The Anatomical Record. doi:10.1002/ar.25341. PMID 37905495. S2CID 264671243.
- ^ Miller, C. V.; Pittman, M.; Wang, X.; Zheng, X.; Bright, J. A. (2023). "Quantitative investigation of pengornithid enantiornithine diet reveals macrocarnivorous ecology evolved in birds by Early Cretaceous". iScience. 26 (3). 106211. Bibcode:2023iSci...26j6211M. doi:10.1016/j.isci.2023.106211. PMC 10009206. PMID 36923002.
- ^ Wang, M. (2023). "A new specimen of Parabohaiornis martini (Avialae: Enantiornithes) sheds light on early avian skull evolution". Vertebrata PalAsiatica. 61 (2): 90–107. doi:10.19615/j.cnki.2096-9899.230217.
- ^ Clark, A. D.; Hu, H.; Benson, R. B. J.; O'Connor, J. K. (2023). "Reconstructing the dietary habits and trophic positions of the Longipterygidae (Aves: Enantiornithes) using neontological and comparative morphological methods". PeerJ. 11. e15139. doi:10.7717/peerj.15139. PMC 10062354. PMID 37009163.
- ^ Liu, S.; Li, Z.; Liu, D.; O'Connor, J. K. (2023). "Quantifying the gastral mass in Early Cretaceous ornithuromorphs (Aves, Ornithothoraces) from the Jehol avifauna". Palaeontology. 66 (5). e12677. Bibcode:2023Palgy..6612677L. doi:10.1111/pala.12677. S2CID 264315198.
- ^ Lowi-Merri, T. M.; Demuth, O. E.; Benito, J.; Field, D. J.; Benson, R. B. J.; Claramunt, S.; Evans, D. C. (2023). "Reconstructing locomotor ecology of extinct avialans: a case study of Ichthyornis comparing sternum morphology and skeletal proportions". Proceedings of the Royal Society B: Biological Sciences. 290 (1994). 20222020. doi:10.1098/rspb.2022.2020. PMC 9993061. PMID 36883281.
- ^ Hu, Qiaohui; Miller, Case Vincent; Snelling, Edward P.; Seymour, Roger S. (2023). "Blood flow rates to leg bones of extinct birds indicate high levels of cursorial locomotion". Paleobiology. 49 (4): 700–711. Bibcode:2023Pbio...49..700H. doi:10.1017/pab.2023.14. hdl:2440/138569. S2CID 258476398.
- ^ Pecsics, Tibor; Csörgő, Tibor (2023). "Aspects of cranial adaptation in foot-propelled diving birds – foraging and visual fields of some piscivorous species". Ornis Hungarica. 31 (2): 110–124. doi:10.2478/orhu-2023-0023.
- ^ Zelenkov, N. V.; Arkhangelsky, M. S. (2023). "New Data on Hesperornithids (Aves: Ornithurae) from the Campanian of the Lower Volga Region (Late Cretaceous, Russia)". Doklady Biological Sciences. 509 (1): 100–102. doi:10.1134/S0012496622600166. PMID 37208574. S2CID 258789466.
- ^ de Souza, Geovane A.; Bulak, Bruno A.; Soares, Marina B.; Sayão, Juliana M.; Weinschütz, Luiz Carlos; Batezelli, Alessandro; Kellner, Alexander W.A. (2023). "The Cretaceous Neornithine record and new Vegaviidae specimens from the López de Bertodano Formation (Upper Maastrichthian) of Vega Island, Antarctic Peninsula". Anais da Academia Brasileira de Ciências. 95 (suppl 3): e20230802. doi:10.1590/0001-3765202320230802. PMID 38088642.
- ^ Álvarez-Herrera, G. P.; Rozadilla, S.; Agnolín, F. L.; Novas, F. E. (2023). "Jaw anatomy of Vegavis iaai (Clarke et al., 2005) from the Late Cretaceous Antarctica, and its phylogenetic implications". Geobios. 83: 11–20. doi:10.1016/j.geobios.2023.03.004. S2CID 259955013.
- ^ Acosta Hospitaleche, C.; O'Gorman, J. P.; Panzeri, K. M. (2023). "A new Cretaceous bird from the Maastrichtian La Colonia Formation (Patagonia, Argentina)". Cretaceous Research. 150. 105595. Bibcode:2023CrRes.15005595A. doi:10.1016/j.cretres.2023.105595. S2CID 259059084.
- ^ Pickford, M.; Al-Kindi, M.; Rajhi, M.; Al Marjibi, T.; Al Rawahi, F. (2023). "Correlation of the Marsawdad Formation, Oman, Late Miocene (Turolian-Ventian), based on fossil avian eggshells". Estudios Geológicos. 79 (2). e153. doi:10.3989/egeol.44974.631.
- ^ Mourer-Chauviré, C.; Pickford, M.; Senut, B. (2023). "New remains of Struthio coppensi, Early Miocene, Namibia" (PDF). Communications of the Geological Survey of Namibia. 26: 21–33.
- ^ Buffetaut, E. (2023). "The Missing Late Pleistocene Ostrich Femur from Zhoukoudian (China): New Information Provided by a Rediscovered Old Cast". Diversity. 15 (2). 265. doi:10.3390/d15020265.
- ^ Jones, Washington W.; Vezzosi, Raúl I.; R. Ernesto, Blanco (2023). "Not too fast: Maximum running speed estimation of the Miocene rheid Opisthodactylus kirchneri (Aves, Rheidae)". Geobios. 83: 39–44. doi:10.1016/j.geobios.2023.03.006. S2CID 259959139.
- ^ Grealy, A.; Miller, G. H.; Phillips, M. J.; Clarke, S. J.; Fogel, M.; Patalwala, D.; Rigby, P.; Hubbard, A.; Demarchi, B.; Collins, M.; Mackie, M.; Sakalauskaite, J.; Stiller, J.; Clarke, J. A.; Legendre, L. J.; Douglass, K.; Hansford, J.; Haile, J.; Bunce, M. (2023). "Molecular exploration of fossil eggshell uncovers hidden lineage of giant extinct bird". Nature Communications. 14 (1). 914. Bibcode:2023NatCo..14..914G. doi:10.1038/s41467-023-36405-3. PMC 9974994. PMID 36854679.
- ^ Fleury, Kane; Burns, Emma; Richards, Marcus; Norton, Kevin; Read, Stephen; Wesley, Rachel; Ewan Fordyce, R.; Wilcken, Klaus (2023). "The moa footprints from the Pliocene – early Pleistocene of Kyeburn, Otago, New Zealand". Journal of the Royal Society of New Zealand. 54 (5): 620–642. doi:10.1080/03036758.2023.2264789. PMC 11459810.
- ^ Piro, A.; Acosta Hospitaleche, C. (2023). "The rhamphotheca of the Eocene pseudo-toothed birds from Antarctica". Historical Biology. 36 (9): 1745–1753. doi:10.1080/08912963.2023.2230584. S2CID 259578452.
- ^ Dobrovolsky, S. (2023). "Bone microstructure of bony-toothed birds (Odontopterygiformes) from the Eocene of Ikove, Ukraine: preliminary paleobiological implications". Historical Biology. 36 (9): 1727–1744. doi:10.1080/08912963.2023.2228335. S2CID 259871568.
- ^ Dobrovolsky, Stanislav; Gorobets, Leonid (2023). "Growth duration, life history and ecological traits of bony-toothed birds (Odontopterygiformes): implications from bone histology". Geo&Bio. 2023 (24): 141–158. doi:10.53452/gb2409.
- ^ Kuo, Pei-Chen; Benson, Roger B. J.; Field, Daniel J. (2023). "The influence of fossils in macroevolutionary analyses of 3D geometric morphometric data: A case study of galloanseran quadrates". Journal of Morphology. 284 (6): e21594. doi:10.1002/jmor.21594. PMID 37183494. S2CID 258367829.
- ^ Zelenkov, N. V. (2023). "Small ducks (Aves: Anatidae) from the early-middle Miocene of Eurasia. 1. A revision of Anas velox Milne-Edwards, 1868 and Anas soporata Kurochkin, 1976". Paleontological Journal. 57 (4): 452–462. Bibcode:2023PalJ...57..452Z. doi:10.1134/S0031030123040159. S2CID 261103528.
- ^ Boev, Zlatozar (2023). "Fossil Record and Distribution of the Hazel Grouse (Tetrastes bonasia) (Linnaeus, 1758) (Phasianidae - Aves) in Bulgaria 549". Proceedings of the Bulgarian Academy of Sciences. 76 (4): 549–553. doi:10.7546/CRABS.2023.04.06. S2CID 258433286.
- ^ Mayr, G.; Göhlich, U. B.; Roček, Z.; Lemierre, A.; Winkler, V.; Georgalis, G. L. (2023). "Reinterpretation of tuberculate cervical vertebrae of Eocene birds as an exceptional anti-predator adaptation against the mammalian craniocervical killing bite". Journal of Anatomy. 244 (3): 402–410. doi:10.1111/joa.13980. PMC 10862156. PMID 37990985. S2CID 265351102.
- ^ Cruz, J. Alberto; Moreno-Flores, Omar; Corona-M, Eduardo; Arroyo-Cabrales, Joaquín (2023). "The first American occurrence of Phoenicopteridae fossil egg and its palaeobiogeographical and palaeoenvironmental implications". Historical Biology: 1–8. doi:10.1080/08912963.2023.2241050. S2CID 260389526.
- ^ Moretti, John A.; Johnson, Eileen (2023). "Small rails from the late Quaternary of the Southern High Plains and their palaeoenvironmental context". Ibis. 165 (4): 1280–1295. doi:10.1111/ibi.13212. S2CID 257909071.
- ^ Verry, Alexander J. F.; Mas-Carrió, Eduard; Gibb, Gillian C.; Dutoit, Ludovic; Robertson, Bruce C.; Waters, Jonathan M.; Rawlence, Nicolas J. (2023). "Ancient mitochondrial genomes unveil the origins and evolutionary history of New Zealand's enigmatic takahē and moho". Molecular Ecology. 33 (3): e17227. doi:10.1111/mec.17227. PMID 38018770.
- ^ Lenser, Karl M.; Worthy, Trevor H. (2023). "Morphometric analysis confirms the presence of the Plains-wanderer (Aves: Pedionomus torquatus) in fossil deposits at Naracoorte Caves, South Australia". Emu - Austral Ornithology. 123 (4): 268–280. Bibcode:2023EmuAO.123..268L. doi:10.1080/01584197.2023.2240346. S2CID 260527394.
- ^ Wu, S.-M.; Worthy, T. H.; Chuang, C.-K.; Lin, C.-H. (2023). "New Pleistocene bird fossils in Taiwan reveal unexpected seabirds in East Asia". Acta Palaeontologica Polonica. 68 (4): 613–624. doi:10.4202/app.01091.2023.
- ^ Haidr, Nadia Soledad (2023). "Ecomorphological variation of the penguin wing". Journal of Morphology. 284 (6): e21588. doi:10.1002/jmor.21588. PMID 37183492. S2CID 258296199.
- ^ Acosta Hospitaleche, C.; Soto-Acuña, S. (2023). "A small penguin cranium (Aves, Spheniscidae) from the Late Miocene of Bahía Inglesa Formation, Atacama Desert, Northern Chile". Comptes Rendus Palevol. 22 (13): 233–244. doi:10.5852/cr-palevol2023v22a13. S2CID 258388724.
- ^ Figueiredo, Silvério; de Carvalho, Carlos Neto; Cachão, Mário; Fonseca, Alexandre (2023-01-09). "A marine bird (sulidae, Aves) from the Langhian (middle Miocene) of Penedo beach (Setúbal Peninsula—SW Portugal) and its paleoenvironmental context". Journal of Iberian Geology. 49 (1): 21–29. Bibcode:2023JIbG...49...21F. doi:10.1007/s41513-022-00203-5. ISSN 1886-7995.
- ^ Ksepka, D. T.; Tennyson, A. J. D. (2023). "Oldest fossil record of Sulidae from New Zealand". Journal of Ornithology. 165 (1): 277–280. Bibcode:2023JOrni.165..277K. doi:10.1007/s10336-023-02117-0. S2CID 263644150.
- ^ Guilherme, E.; D'Apolito, C.; Muniz, F.; Lomba, S. O.; Aldrin, L.; Hsiou, A. S. (2023). "New fossil anhingids from the upper Acre River (Late Miocene of southwestern Amazon)". The Anatomical Record. 307 (6): 2047–2064. doi:10.1002/ar.25329. PMID 37779325. S2CID 263333042.
- ^ Hume, Julian P. (2023). "Osteological and historical data on extinct island night herons (Aves: Ardeidae), with special reference to Ascension Island, the Mascarenes and Bonin Islands". Geobios. 83: 21–38. doi:10.1016/j.geobios.2023.01.009. S2CID 260009824.
- ^ Steinfield, K. R.; Felice, R. N.; Kirchner, M. E.; Knapp, A. (2023). "Carrion converging: Skull shape predicts feeding ecology in vultures". Journal of Zoology. 322 (2): 113–125. doi:10.1111/jzo.13127.
- ^ Sanz, Montserrat; Daura, Joan; Costa, Ana Maria; Araújo, Ana Cristina (2023). "The characterization of bearded vulture (Gypaetus barbatus) coprolites in the archaeological record". Scientific Reports. 13 (1): 57. Bibcode:2023NatSR..13...57S. doi:10.1038/s41598-022-25288-x. PMC 9810590. PMID 36596809.
- ^ Matsuoka, Hiroshige; Hasegawa, Yoshikazu (2023). "The avian remain recorded from the "Felis bed" of Gansuiji Fm. (Hamamatsu, Shizuoka, central Japan) in which the human remains of "older Hamakita Man" was found, is identified as Aegypius monachus (Accipitridae)" (PDF). Bulletin of Gunma Museum of Natural History. 27: 23–29.
- ^ Ramello, Gloria; Delfino, Massimo; Mori, Emiliano; Viviano, Andrea; Pavia, Giulio; Carnevale, Giorgio; Pavia, Marco (2023). "Holocene vertebrate assemblages provide the first evidence for the presence of the barn owl (Tytonidae, Tyto alba) on Socotra Island (Yemen)". Geobios. 83: 85–98. doi:10.1016/j.geobios.2023.03.005. S2CID 259958597.
- ^ Melchor, R. N.; Feola, S. F.; Cardonatto, M. C.; Espinoza, N.; Rojas-Manriquez, M. A.; Herazo, L. (2023). "First terror bird footprints reveal functionally didactyl posture". Scientific Reports. 13 (1). 16474. Bibcode:2023NatSR..1316474M. doi:10.1038/s41598-023-43771-x. PMC 10542783. PMID 37777554.
- ^ Oswald, Jessica A.; Smith, Brian Tilston; Allen, Julie M.; Guralnick, Robert P.; Steadman, David W.; LeFebvre, Michelle J. (2023). "Changes in parrot diversity after human arrival to the Caribbean". Proceedings of the National Academy of Sciences. 120 (41): e2301128120. Bibcode:2023PNAS..12001128O. doi:10.1073/pnas.2301128120. hdl:10919/116533. PMC 10576146. PMID 37748079.
- ^ Stidham, T. A.; O'Connor, J. K.; Li, Z. (2023). "The Pleistocene Zhoukoudian 'Peking Man' site records the first Beijing (China) evidence of the Northern Raven (Corvus corax)". Journal of Ornithology. 165 (1): 269–276. Bibcode:2023JOrni.165..269S. doi:10.1007/s10336-023-02103-6. S2CID 261267886.
- ^ Baumann, C.; Hussain, S. T.; Roblíčková, M.; Riede, F.; Mannino, M. A.; Bocherens, H. (2023). "Evidence for hunter-gatherer impacts on raven diet and ecology in the Gravettian of Southern Moravia". Nature Ecology & Evolution. 7 (8): 1302–1314. Bibcode:2023NatEE...7.1302B. doi:10.1038/s41559-023-02107-8. PMID 37349568. S2CID 259233224.
- ^ Tambussi, Claudia; Dregange, Federico; de Mendoza, Ricardo (2023). ""The present state of knowledge of the Cenozoic birds of Argentina" by Tonni 1980: four decades after". Publicación Electrónica de la Asociación Paleontológica Argentina. 23: 255–295. doi:10.5710/PEAPA.13.08.2022.418. S2CID 258750621.
- ^ Mourer-Chauviré, C.; Pickford, M.; Mocke, H.; Nduutepo, A. (2023). "Small birds (Psittaculidae, Galliformes and Passeri) from the Early Miocene of Namibia" (PDF). Communications of the Geological Survey of Namibia. 26: 10–20.
- ^ Silva-Martínez, Ana Frida; Zúñiga-Vega, J. Jaime; Arroyo-Cabrales, Joaquín; Sánchez-González, Luis A. (2023). "Changes in body size in some bird species from the Yucatán peninsula since the Late Pleistocene". International Journal of Osteoarchaeology. 33 (4): 619–630. doi:10.1002/oa.3219. S2CID 257211096.
- ^ Garcia-Fermet, Thomas; Testu, Agnès; Moigne, Anne-Marie; Saos, Thibaud; GréGoire, Sophie (2023). "The bird remains from La Crouzade Cave (Gruissan, Aude): The mixed origin of a Middle Palaeolithic bone accumulation". Quaternary Environments and Humans. 1: 100001. Bibcode:2023QuEH....100001G. doi:10.1016/j.qeh.2023.100001.
- ^ Neto de Carvalho, C.; Belo, J.; Figueiredo, S.; Cunha, P. P.; Muñiz, F.; Belaústegui, Z.; Cachão, M.; Rodriguez-Vidal, J.; Cáceres, L. M.; Baucon, A.; Murray, A. S.; Buylaert, J.-P.; Zhang, Y.; Ferreira, C.; Toscano, A.; Gómez, P.; Ramírez, S.; Finlayson, G.; Finlayson, S.; Finlayson, C. (2023). "Coastal raptors and raiders: New bird tracks in the Pleistocene of SW iberian Peninsula". Quaternary Science Reviews. 313. 108185. Bibcode:2023QSRv..31308185N. doi:10.1016/j.quascirev.2023.108185. S2CID 259572925.
- ^ Gala, M.; Laroulandie, V.; Lenoble, A. (2023). "Bird communities from the Guadeloupe islands over the last 30,000 yrs". Quaternaire. 34 (3): 161–203. doi:10.4000/quaternaire.18254.
- ^ Martill, D. M.; Frey, E.; Tischlinger, H.; Mäuser, M.; Rivera-Sylva, H. E.; Vidovic, S. U. (2023). "A new pterodactyloid pterosaur with a unique filter-feeding apparatus from the Late Jurassic of Germany". PalZ. 97 (2): 383–424. Bibcode:2023PalZ...97..383M. doi:10.1007/s12542-022-00644-4. S2CID 256166586.
- ^ Jiang, Shunxing; Song, Junyi; Zhang, Xinjun; Cheng, Xin; Wang, Xiaolin (2023-11-15). "A new pterosaur from the early stage of the Jehol biota in China, with a study on the relative thickness of bone walls". Heliyon. 9 (12). E22370. Bibcode:2023Heliy...922370J. doi:10.1016/j.heliyon.2023.e22370. PMC 10709016. PMID 38076164.
- ^ Zhang, X.; Jiang, S.; Kellner, A. W. A.; Cheng, X.; Costa, F. R.; Wang, X. (2023). "A new species of Eopteranodon (Pterodactyloidea, Tapejaridae) from the Lower Cretaceous Yixian Formation of China". Cretaceous Research. 149. 105573. Bibcode:2023CrRes.14905573Z. doi:10.1016/j.cretres.2023.105573. S2CID 258531568.
- ^ Pêgas, R. V.; Zhoi, X.; Jin, X.; Wang, K.; Ma, W. (2023). "A taxonomic revision of the Sinopterus complex (Pterosauria, Tapejaridae) from the Early Cretaceous Jehol Biota, with the new genus Huaxiadraco". PeerJ. 11. e14829. doi:10.7717/peerj.14829. PMC 9922500. PMID 36788812.
- ^ Fernandes, A. E.; Beccari, V.; Kellner, A. W. A.; Mateus, O. (2023). "A new gnathosaurine (Pterosauria, Archaeopterodactyloidea) from the Late Jurassic of Portugal". PeerJ. 11. e16048. doi:10.7717/peerj.16048. PMC 10512962. PMID 37744218.
- ^ a b Wang, X.; Kellner, A. W. A.; Jiang, S.; Chen, H.; Costa, F. R.; Cheng, X.; Zhang, X.; Vila Nova, B. C.; Campos, D. A.; Sayão, J. M.; Rodrigues, T.; Bantim, R. A. M.; Saraiva, A. A. F.; Zhou, Z. (2023). "A new toothless pterosaur from the Early Cretaceous Jehol Biota with comments on the Chaoyangopteridae". Scientific Reports. 13 (1). 22642. Bibcode:2023NatSR..1322642W. doi:10.1038/s41598-023-48076-7. PMC 10739979. PMID 38129429.
- ^ Hone, David W. E.; Lauer, René; Lauer, Bruce; Spindler, Frederik (2023-07-08). "Petrodactyle wellnhoferi gen. et sp. nov.: A new and large ctenochasmatid pterosaur from the Late Jurassic of Germany". Palaeontologia Electronica. 26 (2): 1–28. doi:10.26879/1251. ISSN 1094-8074. S2CID 259895088.
- ^ Ji, S.; Zhang, L.; Lu, F. (2023). "A new species of chaoyangopterid pterosaur from the Early Cretaceous in western Liaoning, People's Republic of China". Acta Geologica Sinica. 97. 2023322. doi:10.19762/j.cnki.dizhixuebao.2023322.
- ^ Yu, Y.; Zhang, C.; Xu, X. (2023). "Complex macroevolution of pterosaurs". Current Biology. 33 (4): 770–779.e4. Bibcode:2023CBio...33E.770Y. doi:10.1016/j.cub.2023.01.007. PMID 36787747. S2CID 256831564.
- ^ Hone, David (2023). "The anatomy and diversity of the pterosaurian sternum". Palaeontologia Electronica. 26 (1): Article number 26.1.a12. doi:10.26879/1261. S2CID 258273168.
- ^ Yang, Z.; Jiang, B.; Benton, M. J.; Xu, X.; McNamara, M. E.; Hone, D. W. E. (2023). "Allometric wing growth links parental care to pterosaur giantism". Proceedings of the Royal Society B: Biological Sciences. 290 (2003). 20231102. doi:10.1098/rspb.2023.1102. PMC 10354479. PMID 37464754.
- ^ Pentland, A. H.; Poropat, S. F. (2023). "A review of the Jurassic and Cretaceous Gondwanan pterosaur record". Gondwana Research. 119: 341–383. Bibcode:2023GondR.119..341P. doi:10.1016/j.gr.2023.03.005. S2CID 257685507.
- ^ Smith, R. E.; Ibrahim, N.; Longrich, N.; Unwin, D. M.; Jacobs, M. L.; Williams, C. J.; Zouhri, S.; Martill, D. M. (2023). "The pterosaurs of the Cretaceous Kem Kem Group of Morocco". PalZ. 97 (3): 519–568. Bibcode:2023PalZ...97..519S. doi:10.1007/s12542-022-00642-6. S2CID 256608633.
- ^ Jagielska, N.; Challands, T. J.; O'Sullivan, M.; Ross, D. A.; Fraser, N. C.; Wilkinson, M.; Brusatte, S. L. (2023). "New postcranial remains from the Lealt Shale Formation of the Isle of Skye, Scotland, showcase hidden pterosaur diversity in the Middle Jurassic". Scottish Journal of Geology. 59 (1–2): 001. Bibcode:2023ScJG...59....1J. doi:10.1144/sjg2023-001. hdl:20.500.11820/8bc004a4-ab80-4f9f-965d-f211f18e9876. S2CID 258232744.
- ^ Henkemeier, N.; Jäger, K. R. K.; Sander, P. M. (2023). "Redescription of soft tissue preservation in the holotype of Scaphognathus crassirostris (Goldfuß, 1831) using reflectance transformation imaging". Palaeontologia Electronica. 26 (2). 26.2.a16. doi:10.26879/1070.
- ^ Pentland, A. H.; Vickers-Rich, P.; Rich, T. H.; Rigby, S. L.; Poropat, S. F. (2023). "Oldest pterosaur remains from Australia: evidence from the Lower Cretaceous (lower Albian) Eumeralla Formation of Victoria". Historical Biology. 36 (7): 1188–1195. doi:10.1080/08912963.2023.2201827.
- ^ Cerda, I.; Codorniú, L. (2023). "Palaeohistology reveals an unusual periodontium and tooth implantation in a filter-feeding pterodactyloid pterosaur, Pterodaustro guinazui, from the Lower Cretaceous of Argentina". Journal of Anatomy. 243 (4): 579–589. doi:10.1111/joa.13878. PMC 10485577. PMID 37059589. S2CID 258153901.
- ^ Sweetman, S. C. (2023). "Pterosaur teeth from the Lower Cretaceous (Valanginian) Cliff End Bone Bed, Wadhurst Clay Formation, Wealden Supergroup of southern England, and their possible affinities". Cretaceous Research. 151. 105622. Bibcode:2023CrRes.15105622S. doi:10.1016/j.cretres.2023.105622. S2CID 259731678.
- ^ Ozeki, M.; Unwin, D. M.; Bell, P. R.; Li, D.; Xing, L. (2023). "A new pterosaur specimen from the Lower Cretaceous Yixian Formation of Liaoning Province, China: The oldest fossil record of Nurhachius". Historical Biology. 36 (8): 1625–1638. doi:10.1080/08912963.2023.2222127. S2CID 259677697.
- ^ Wu, Q.; Chen, H.; Li, Z.; Jiang, S.; Wang, X.; Zhou, Z. (2023). "The morphology and histology of the pectoral girdle of Hamipterus (Pterosauria), from the Early Cretaceous of Northwest China". The Anatomical Record. doi:10.1002/ar.25167. PMID 36787121. S2CID 256844449.
- ^ Chen, H.; Li, Z.; Jiang, S.; Wu, Q.; Gong, Y.; Zhu, X.; Wang, X. (2023). "A preliminary analysis of dental microstructure in Hamipterus (Pterosauria, Pterodactyloidea)". The Anatomical Record. doi:10.1002/ar.25289. PMID 37477189. S2CID 259993331.
- ^ Richards, Timothy M.; Stumkat, Paul E.; Salisbury, Steven W. (2023-10-06). "A second specimen of the pterosaur Thapunngaka shawi from the Lower Cretaceous (upper Albian) Toolebuc Formation of North West Queensland, Australia". Cretaceous Research. 154: 105740. doi:10.1016/j.cretres.2023.105740.
- ^ Frey, E.; Martill, D. M.; Zouhri, S. (2023). "Distinctive azhdarchoid pterosaur jaws from the mid-Cretaceous Cambridge Greensand of eastern England and the Kem Kem Group of Morocco". Proceedings of the Geologists' Association. 134 (3): 269–275. Bibcode:2023PrGA..134..269S. doi:10.1016/j.pgeola.2023.03.002. S2CID 257977095.
- ^ Song, J.; Jiang, S.; Wang, X. (2023). "Pterosaur remains from uppermost Lower Cretaceous (Albian) of China, with comments on the femoral osteological correlates for thigh muscles". Cretaceous Research. 150. 105588. Bibcode:2023CrRes.15005588S. doi:10.1016/j.cretres.2023.105588. S2CID 258881639.
- ^ Zhou, C.-F.; Miao, C.; Andres, B. (2023). "New data on the cranial morphology of the tapejarid Sinopterus from the Early Cretaceous Jehol Biota". Historical Biology. 36 (5): 1050–1057. doi:10.1080/08912963.2023.2202219. S2CID 258255469.
- ^ Cerqueira, G. M.; Müller, R. T.; Pinheiro, F. L. (2023). "On the phylogenetic affinities of the tapejarid pterosaur 'Tupuxuara deliradamus' from the Lower Cretaceous of Brazil". Historical Biology. 36 (3): 677–682. doi:10.1080/08912963.2023.2180741. S2CID 257064743.
- ^ de Araújo, E. V.; Bantim, R. A. M.; Holgado, B.; Sayão, J. M.; Weinschütz, L. C.; Kellner, A. (2023). "Osteohistological characterization and ontogeny of Caiuajara dobruskii (Pterosauria, Pterodactyloidea, Tapejaridae)". Historical Biology. 36 (7): 1204–1219. doi:10.1080/08912963.2023.2207193. S2CID 258775846.
- ^ Bennett, S. C. (2001). "The osteology and functional morphology of the Late Cretaceous pterosaur Pteranodon Part I. General description of osteology". Palaeontographica Abteilung A. 260 (1–6): 1–112. Bibcode:2001PalAA.260....1B. doi:10.1127/pala/260/2001/1. S2CID 90380603.
- ^ Bennett, S. C. (2023). "Wing phalanges of a ?thalassodromine pterosaur from the Aptian-Albian Antlers Formation of Texas, USA". Cretaceous Research. 154. 105771. doi:10.1016/j.cretres.2023.105771. S2CID 265140117.
- ^ Agnolín, F. L.; Rozadilla, S.; Juárez-Valieri, R. D.; Meso, J. G. (2023). "Oldest azhdarchid (Pterosauria) record from South America". Revista del Museo Argentino de Ciencias Naturales. Nueva Series. 25 (2): 309–314. doi:10.22179/REVMACN.25.825.
- ^ Sokolskyi, T. (2023). "First occurrence of pterosaurs in Ukraine from the Albian (Lower Cretaceous) Burim Formation, Kaniv Natural Reserve". Journal of Vertebrate Paleontology. 43 (1). e2238000. doi:10.1080/02724634.2023.2238000. S2CID 260829897.
- ^ Müller, R. T.; Garcia, M. S. (2023). "A new silesaurid from Carnian beds of Brazil fills a gap in the radiation of avian line archosaurs". Scientific Reports. 13 (1). 4981. Bibcode:2023NatSR..13.4981M. doi:10.1038/s41598-023-32057-x. PMC 10090097. PMID 37041170.
- ^ Nesbitt, Sterling J.; Patellos, Emily; Kammerer, Christian F.; Ranivoharimanana, Lovasoa; Wyss, Andre´ R.; Flynn, John J. (25 July 2023). "The earliest-diverging avemetatarsalian: a new osteoderm-bearing taxon from the Triassic (?Earliest Late Triassic) of Madagascar and the composition of avemetatarsalian assemblages prior to the radiation of dinosaurs". Zoological Journal of the Linnean Society. 199 (2): 327–353. doi:10.1093/zoolinnean/zlad038.
- ^ Müller, R. T.; Ezcurra, M. D.; Garcia, M. S.; Agnolín, F. L.; Stocker, M. R.; Novas, F. E.; Soares, M. B.; Kellner, A. W. A.; Nesbitt, S. J. (2023). "New reptile shows dinosaurs and pterosaurs evolved among diverse precursors". Nature. 620 (7974): 589–594. Bibcode:2023Natur.620..589M. doi:10.1038/s41586-023-06359-z. PMID 37587301. S2CID 260929813.
- ^ Foffa, D.; Nesbitt, S. J.; Butler, R. J.; Brusatte, S. L.; Walsh, S.; Fraser, N. C.; Barrett, P. M. (2023). "The osteology of the Late Triassic reptile Scleromochlus taylori from μCT data". The Anatomical Record. 307 (4): 1113–1146. doi:10.1002/ar.25335. hdl:20.500.11820/2411a888-1efb-42d1-a498-fc031145ed86. PMID 37846180.
- ^ Bronzati, M.; Langer, M. C.; Ezcurra, M. D.; Stocker, M. R.; Nesbitt, S. J. (2023). "Braincase and neuroanatomy of the lagerpetid Dromomeron gregorii (Archosauria, Pterosauromorpha) with comments on the early evolution of the braincase and associated soft tissues in Avemetatarsalia". The Anatomical Record. 307 (4): 1147–1174. doi:10.1002/ar.25334. PMID 37794742.
- ^ Mestriner, G.; Marsola, J. C. A.; Nesbitt, S. J.; Da-Rosa, Á. A. S.; Langer, M. (2023). "Anatomy and phylogenetic affinities of a new silesaurid assemblage from the Carnian beds of south Brazil". Journal of Vertebrate Paleontology. 43 (1). e2232426. doi:10.1080/02724634.2023.2232426. S2CID 261157405.
- ^ Wang, Y.; Claessens, L. P. A. M.; Sullivan, C. (2023). "Deep reptilian evolutionary roots of a major avian respiratory adaptation". Communications Biology. 6 (1). 3. doi:10.1038/s42003-022-04301-z. PMC 9845227. PMID 36650231.
- ^ Aureliano, T.; Ghilardi, A. M.; Fernandes, M. A.; Ricardi-Branco, F. S. (2023). "Air sac attachments or tendon scars: the distinction between soft tissue traces in archosaur bone". Zoological Journal of the Linnean Society. doi:10.1093/zoolinnean/zlac103.
- ^ De-Oliveira, T.; Pretto, F. A.; Müller, R. T.; Pinheiro, F. L.; Kerber, L. (2023). "On the presence of a carnivore archosaur in the São Luiz site, an iconic Late Triassic fossiliferous locality from Brazil". Journal of South American Earth Sciences. 104604. doi:10.1016/j.jsames.2023.104604. S2CID 263320741.
- ^ Abrahams, M.; Bordy, E. M. (2023). "The oldest fossil bird-like footprints from the upper Triassic of southern Africa". PLOS ONE. 18 (11). e0293021. Bibcode:2023PLoSO..1893021A. doi:10.1371/journal.pone.0293021. PMC 10686444. PMID 38019739.
- ^ Figueiredo, S. D.; Neto de Carvalho, C.; Cunha, P. P.; Duarte, L. V.; Fonseca, A.; Monteiro, C.; Forte, J. (2023). "The first dinosaurs in Iberia: a new dinosaur tracksite from the Sinemurian (Lower Jurassic) of Portugal". Historical Biology: 1–14. doi:10.1080/08912963.2023.2256751. S2CID 262198094.
- ^ Xing, L.-D.; Lockley, M. G.; Tong, B.-L.; Klein, H.; Liu, C.; Persons, W. S. (2023). "The Middle–Upper Jurassic dinosaur-pterosaur fauna in Shandong Province, China: Evidence from ichnology". Journal of Palaeogeography. 12 (3): 419–433. Bibcode:2023JPalG..12..419X. doi:10.1016/j.jop.2023.05.001. S2CID 258643815.
- ^ Zheng, D.; Chang, S.-C.; Ramezani, J.; Xu, X.; Xu, H.; Wang, H.; Pei, R.; Fang, Y.; Wang, J.; Wang, B.; Zhang, H. (2023). "Calibrating the Early Cretaceous Urho Pterosaur Fauna in Junggar Basin and implications for the evolution of the Jehol Biota". GSA Bulletin. doi:10.1130/B36795.1. S2CID 258628286.
- ^ Juarez, M.; Hechenleitner, E. M.; Martinelli, A. G.; Rocher, S.; Fiorelli, L. E. (2023). "First record of abelisaurid theropods and a peirosaurid crocodyliform from the Upper Cretaceous of Precordillera of La Rioja, NW Argentina". Cretaceous Research. 152. 105679. Bibcode:2023CrRes.15205679J. doi:10.1016/j.cretres.2023.105679. S2CID 261014414.
- ^ Mohr, Sydney R.; Acorn, John H.; Currie, Philip J (2023). "Putative avian teeth from the Late Cretaceous of Alberta, Canada, are more likely from crocodilians". PLOS ONE. 18 (3): e0283581. Bibcode:2023PLoSO..1883581M. doi:10.1371/journal.pone.0283581. PMC 10047536. PMID 36976814.
- ^ Roy, Arindam; Pittman, Michael; Kaye, Thomas G.; Saitta, Evan T. (2023). "Sediment-encased pressure–temperature maturation experiments elucidate the impact of diagenesis on melanin-based fossil color and its paleobiological implications". Paleobiology. 49 (4): 712–732. Bibcode:2023Pbio...49..712R. doi:10.1017/pab.2023.11. S2CID 258573917.
- ^ Slater, T. S.; Edwards, N. P.; Webb, S. M.; Zhang, F.; McNamara, M. E. (2023). "Preservation of corneous β-proteins in Mesozoic feathers". Nature Ecology & Evolution. 7 (10): 1706–1713. Bibcode:2023NatEE...7.1706S. doi:10.1038/s41559-023-02177-8. PMID 37735563. S2CID 262125827.
- ^ Mainwaring, Mark C.; Medina, Iliana; Tobalske, Bret W.; Hartley, Ian R.; Varricchio, David J.; Hauber, Mark E. (2023). "The evolution of nest site use and nest architecture in modern birds and their ancestors". Philosophical Transactions of the Royal Society B: Biological Sciences. 378 (1884). doi:10.1098/rstb.2022.0143. PMC 10331912. PMID 37427466.
- ^ Fernández, M. S.; Piazza, M.; Simoncini, M. S. (2023). "Do ontogenetic changes during incubation interfere with the interpretation of incubation mode in dinosaur eggs?". Historical Biology: 1–7. doi:10.1080/08912963.2023.2257956. S2CID 262182129.