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Balaenognathus maeuseri gen. et sp. nov.: comparative interpretive drawings of the skulls of suspension feeding ctenochasmatoid pterosaurs in dorsal aspect. Balaenognathus this paper; Pterodaustro based on Bonaparte (1978); Plateleorhynchus based on Howse and Milner (1995); Gnathosaurus based on specimen JME-SOS 4580; Ctenochasma based on (2007 Fig. 2F)

Balaenognathus maeuseri gen. et sp. nov.: comparative interpretive drawings of the skulls of suspension feeding ctenochasmatoid pterosaurs in dorsal aspect. Balaenognathus this paper; Pterodaustro based on Bonaparte (1978); Plateleorhynchus based on Howse and Milner (1995); Gnathosaurus based on specimen JME-SOS 4580; Ctenochasma based on (2007 Fig. 2F)

feeding drawing specimen Balaenognathus +6
Identifier: annalsofmedicalh01pack (find matches)
Title: Annals of medical history
Year: 1917 (1910s)
Authors:  Packard, Francis R. (Francis Randolph), 1870-1950
Subjects:  Medicine
Publisher:  New York P.B. Hoeber
Contributing Library:  Gerstein - University of Toronto
Digitizing Sponsor:  University of Toronto

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ail strongly Hexed, and the toescontracted and appressed. The whole atti-tude strongly suggests a spastic distress,possibly brought on by some form ofpoisoning of the central nervous system,from infection or the deglutition of somepoisonous substance. 14. Osteomalacia is evidently the causeof the hypertrophy of the bones of Lim-nocyron potens, an early carnivore from theWashakie Eocene of Wyoming, nearly3,000,000 years old. MATERIALS AND METHODS The material described in the presentpaper has been loaned the writer lor de-scription by the Field Museum of Chii Osborn: Hull. Amcr. \lus. Natl. Hist., 1917,vol. 35. !>• 733. P>- 28. Studies in Paleopathology 393 by the American Museum of Natural His-tory of New York City, by Walker Museumof the University of Chicago, and by the Uni-versity of Kansas Natural History Museum. made by the well-known petrographic meth-ods so common in all geological labora-tories. The diagnoses, where they are at-tempted, arc made from comparisons of the
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Fig. 20. The skeleton of Strutbiomimus altus, a small dinosaur from the BeliyRiver series (Cretaceous), Red Deer River, Alberta, Canada, now regarded as ofapproximately the same age as the Judith River series. The unique feature ofthe skull is the total absence of teeth, with a size of skull one-third larger thanthe ostrich and a length of body of about fifteen feet. The position of the skeletonis decidedly that of the opisthotonos which may be regarded as an indication ofdisease. (After Osborn). A beautiful specimen of an osteoma, theonly one known so far, on the vertebra of aKansas Cretaceous mosasaur, was given thewriter by Dr. J. M. Armstrong of St. Paul.The writer expresses his obligations to thegentlemen connected with the above-men-tioned institutions and to Dr. Armstrong.The methods used are a combination ofprocedures in the various lines involved.Microscopic sections, which can be madethin enough for immersion lens study, are material with similar lesions in recent hu-man mat

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Identifier: annalsofmedicalh01pack (find matches) Title: Annals of medical history Year: 1917 (1910s) Authors: Packard, Francis R. (Francis Randolph), 1870-1950 Subjects: Medicine Publisher: New York P.B. Hoeber Contributing Library: Gerstein - University of Toronto Digitizing Sponsor: University of Toronto View Book Page: Book Viewer About This Book: Catalog Entry View All Images: All Images From Book Click here to view book online to see this illustration in context in a browseable online version of this book. Text Appearing Before Image: ail strongly Hexed, and the toescontracted and appressed. The whole atti-tude strongly suggests a spastic distress,possibly brought on by some form ofpoisoning of the central nervous system,from infection or the deglutition of somepoisonous substance. 14. Osteomalacia is evidently the causeof the hypertrophy of the bones of Lim-nocyron potens, an early carnivore from theWashakie Eocene of Wyoming, nearly3,000,000 years old. MATERIALS AND METHODS The material described in the presentpaper has been loaned the writer lor de-scription by the Field Museum of Chii Osborn: Hull. Amcr. \lus. Natl. Hist., 1917,vol. 35. !>• 733. P>- 28. Studies in Paleopathology 393 by the American Museum of Natural His-tory of New York City, by Walker Museumof the University of Chicago, and by the Uni-versity of Kansas Natural History Museum. made by the well-known petrographic meth-ods so common in all geological labora-tories. The diagnoses, where they are at-tempted, arc made from comparisons of the Text Appearing After Image: Fig. 20. The skeleton of Strutbiomimus altus, a small dinosaur from the BeliyRiver series (Cretaceous), Red Deer River, Alberta, Canada, now regarded as ofapproximately the same age as the Judith River series. The unique feature ofthe skull is the total absence of teeth, with a size of skull one-third larger thanthe ostrich and a length of body of about fifteen feet. The position of the skeletonis decidedly that of the opisthotonos which may be regarded as an indication ofdisease. (After Osborn). A beautiful specimen of an osteoma, theonly one known so far, on the vertebra of aKansas Cretaceous mosasaur, was given thewriter by Dr. J. M. Armstrong of St. Paul.The writer expresses his obligations to thegentlemen connected with the above-men-tioned institutions and to Dr. Armstrong.The methods used are a combination ofprocedures in the various lines involved.Microscopic sections, which can be madethin enough for immersion lens study, are material with similar lesions in recent hu-man mat Note About Images Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.

bone vertebra museum Canada +10
The holotype and only known specimen of the hauffiopterygian leptonectid, Xiphodracon goldencapensis (ROM VP52596) from Golden Cap, between Charmouth and Seatown, Dorset, UK. The skeleton is exposed in ventrolateral view. The skull has been fully prepared free of matrix whereas most of the skeleton is still in matrix. The left (upper) forefin has been prepared so that it is three-dimensionally preserved and projects upwards. Scale bar represents 20 cm.

The holotype and only known specimen of the hauffiopterygian leptonectid, Xiphodracon goldencapensis (ROM VP52596) from Golden Cap, between Charmouth and Seatown, Dorset, UK. The skeleton is exposed in ventrolateral view. The skull has been fully prepared free of matrix whereas most of the skeleton is still in matrix. The left (upper) forefin has been prepared so that it is three-dimensionally preserved and projects upwards. Scale bar represents 20 cm.

scale United Kingdom holotype specimen +5
Known skull material of Kuru kulla (gen. et sp. nov. Napoli et al. 2022) - premaxilla, dentary, surangular, lacrimal, and teeth - shown with a speculative restoration of the remainder of the skull based on the related taxon Velociraptor mongoliensis.  Known skull material is shown in light grey and labeled; unknown parts of the skull are shown in dark grey.

Known skull material of Kuru kulla (gen. et sp. nov. Napoli et al. 2022) - premaxilla, dentary, surangular, lacrimal, and teeth - shown with a speculative restoration of the remainder of the skull based on the related taxon Velociraptor mongoliensis. Known skull material is shown in light grey and labeled; unknown parts of the skull are shown in dark grey.

Kuru Velociraptor skull
A skull reconstruction and cranial bones from Shaochilong maortuensis, a small-bodied mid Cretaceous (Turonian) carcharodontosauri-an theropod from Inner Mongolia, China. A, skull reconstruction (courtesy of Brett Booth); B, right maxilla in lateral view (IVPP V.2885.4); C, braincase and skull roof in dorsal view (IVPP V.2885.1-2). Scale bars equal 5 centimeters.

A skull reconstruction and cranial bones from Shaochilong maortuensis, a small-bodied mid Cretaceous (Turonian) carcharodontosauri-an theropod from Inner Mongolia, China. A, skull reconstruction (courtesy of Brett Booth); B, right maxilla in lateral view (IVPP V.2885.4); C, braincase and skull roof in dorsal view (IVPP V.2885.1-2). Scale bars equal 5 centimeters.

bone scale China Mongolia +4
Dinosaur National Monument is a United States National Monument located on the southeast flank of the Uinta Mountains on the border between Colorado and Utah at the confluence of the Green and Yampa Rivers. Although most of the monument area is in Moffat County, Colorado, the Dinosaur Quarry is located in Utah just to the north of the town of Jensen, Utah.
The nearest communities are Jensen, Utah, and Dinosaur, Colorado. The park contains over 800 paleontological sites and has fossils of dinosaurs including Allosaurus, Deinonychus, Abydosaurus (a nearly complete skull, lower jaws and first four neck vertebrae of the specimen DINO 16488 found here at the base of the Mussentuchit Member of the Cedar Mountain Formation is the holotype for the description) and various long-neck, long-tail sauropods. It was declared a National Monument on October 4, 1915.
The rock layer enclosing the fossils is a sandstone and conglomerate bed of alluvial or river bed origin known as the Morrison Formation from the Jurassic Period some 150 million years old. The dinosaurs and other ancient animals were carried by the river system which eventually entombed their remains in Utah.
The pile of sediments were later buried and lithified into solid rock. The layers of rock were later uplifted and tilted to their present angle by the mountain building forces that formed the Uintas during the Laramide orogeny. The relentless forces of erosion exposed the layers at the surface to be found by paleontologists.
The dinosaur fossil beds (bone beds) were discovered in 1909 by Earl Douglass, a paleontologist working and collecting for the Carnegie Museum of Natural History. He and his crews excavated thousands of fossils and shipped them back to the museum in Pittsburgh, Pennsylvania for study and display. President Woodrow Wilson proclaimed the dinosaur beds as Dinosaur National Monument in 1915. The monument boundaries were expanded in 1938 from the original 80-acre (320,000 m2) tract surrounding the dinosaur quarry in Utah, to its present extent of over 200,000 acres (800 km²) in Utah and Colorado, encompassing the spectacular river canyons of the Green and Yampa.
Though lesser-known than the fossil beds, the petroglyphs in Dinosaur National Monument are another treasure the monument holds. Due to problems with vandals, many of the sites are not listed on area maps.
The "Wall of Bones" located within the Dinosaur Quarry building in the park consists of a steeply tilted (67° from horizontal) rock layer which contains hundreds of dinosaur fossils. The enclosing rock has been chipped away to reveal the fossil bones intact for public viewing. In July 2006, the Quarry Visitor Center was closed due to structural problems that since 1957 had plagued the building because it was built on unstable clay. The decision was made to build a new facility elsewhere in the monument to house the visitor center and administrative functions, making it easier to resolve the structural problems of the quarry building while still retaining a portion of the historic Mission 66 era exhibit hall. It was announced in April 2009 that Dinosaur National Monument would receive $13.1 million to refurbish and reopen the gallery as part of the Obama administration's $750 billion stimulus plan. The Park Service successfully rebuilt the Quarry Exhibit Hall, supporting its weight on 70-foot steel micropile columns that extend to the bedrock below the unstable clay. The Dinosaur Quarry was reopened in Fall 2011.
en.wikipedia.org/wiki/Dinosaur_National_Monument

en.wikipedia.org/wiki/Wikipedia:Text_of_Creative_Commons_...

Dinosaur National Monument is a United States National Monument located on the southeast flank of the Uinta Mountains on the border between Colorado and Utah at the confluence of the Green and Yampa Rivers. Although most of the monument area is in Moffat County, Colorado, the Dinosaur Quarry is located in Utah just to the north of the town of Jensen, Utah. The nearest communities are Jensen, Utah, and Dinosaur, Colorado. The park contains over 800 paleontological sites and has fossils of dinosaurs including Allosaurus, Deinonychus, Abydosaurus (a nearly complete skull, lower jaws and first four neck vertebrae of the specimen DINO 16488 found here at the base of the Mussentuchit Member of the Cedar Mountain Formation is the holotype for the description) and various long-neck, long-tail sauropods. It was declared a National Monument on October 4, 1915. The rock layer enclosing the fossils is a sandstone and conglomerate bed of alluvial or river bed origin known as the Morrison Formation from the Jurassic Period some 150 million years old. The dinosaurs and other ancient animals were carried by the river system which eventually entombed their remains in Utah. The pile of sediments were later buried and lithified into solid rock. The layers of rock were later uplifted and tilted to their present angle by the mountain building forces that formed the Uintas during the Laramide orogeny. The relentless forces of erosion exposed the layers at the surface to be found by paleontologists. The dinosaur fossil beds (bone beds) were discovered in 1909 by Earl Douglass, a paleontologist working and collecting for the Carnegie Museum of Natural History. He and his crews excavated thousands of fossils and shipped them back to the museum in Pittsburgh, Pennsylvania for study and display. President Woodrow Wilson proclaimed the dinosaur beds as Dinosaur National Monument in 1915. The monument boundaries were expanded in 1938 from the original 80-acre (320,000 m2) tract surrounding the dinosaur quarry in Utah, to its present extent of over 200,000 acres (800 km²) in Utah and Colorado, encompassing the spectacular river canyons of the Green and Yampa. Though lesser-known than the fossil beds, the petroglyphs in Dinosaur National Monument are another treasure the monument holds. Due to problems with vandals, many of the sites are not listed on area maps. The "Wall of Bones" located within the Dinosaur Quarry building in the park consists of a steeply tilted (67° from horizontal) rock layer which contains hundreds of dinosaur fossils. The enclosing rock has been chipped away to reveal the fossil bones intact for public viewing. In July 2006, the Quarry Visitor Center was closed due to structural problems that since 1957 had plagued the building because it was built on unstable clay. The decision was made to build a new facility elsewhere in the monument to house the visitor center and administrative functions, making it easier to resolve the structural problems of the quarry building while still retaining a portion of the historic Mission 66 era exhibit hall. It was announced in April 2009 that Dinosaur National Monument would receive $13.1 million to refurbish and reopen the gallery as part of the Obama administration's $750 billion stimulus plan. The Park Service successfully rebuilt the Quarry Exhibit Hall, supporting its weight on 70-foot steel micropile columns that extend to the bedrock below the unstable clay. The Dinosaur Quarry was reopened in Fall 2011. en.wikipedia.org/wiki/Dinosaur_National_Monument en.wikipedia.org/wiki/Wikipedia:Text_of_Creative_Commons_...

bone description museum United States +13
Life restoration of the Triassic ichthyosaur Callawayia neoscapularis. Three specimens of this ichthyosaur are known, the holotype, ROM 41993, and two referred specimens, TMP 94.380.11 and 94.382.2. The skull is primarily based on ROM 41993, cross-checked against TMP 94.380.11 and TMP 94.382.2. The vertebral column is based primarily on TMP 94.382.2 as it is the most complete of these specimens, while the ribs were based on ROM 41993. The forelimbs were mainly based on those of ROM 41993, with TMP 94.380.11 used to determine their breadth. The hindlimbs were based on TMP 94.380.11, especially the more complete right hindlimb.
ROM 41993 was cross-scaled with TMP 94.380.11 by the dimensions of the forelimb epipodials, which produced similar vertebral dimensions. The two TMP specimens were cross-scaled based on femoral length, also producing similar vertebral dimensions. Nicholls & Manabe (2001) stated that no wedge-shaped caudal centra supporting a tailbend were found and that there was no evidence of a bend being present, though considered that they might have existed in the gap in the preserved caudals. Since various other Triassic ichthyosaurs have since been found to have tail bends, one was illustrated here. A modest downturn of roughly 15° was illustrated, comparable to that in Guanlingsaurus, and the location of the bend within the gap in the preserved vertebrae matches well with the location of the bend in Guizhouichthyosaurus.

References
McGowan, C. (1994). "A new species of Shastasaurus (Reptilia: Ichthyosauria) from the Triassic of British Columbia: The most complete exemplar of the genus". Journal of Vertebrate Paleontology 14 (2): 168–179. DOI:10.1080/02724634.1994.10011550.
Nicholls, E. L.; Manabe, M. (2001). "A new genus of ichthyosaur from the Late Triassic Pardonet Formation of British Columbia: Bridging the Triassic-Jurassic gap". Canadian Journal of Earth Sciences 38 (6): 983–1002.
Ji, C.; Jiang, D.Y.; Hao, W.; Sun, Y. (2011). "True tailbend occurred in the Late Triassic: Evidence from ichthyosaur skeletons of South China". Acta Scientiarum Naturalium Universitatis Pekinensis 47 (2): 309–314.
Shang, Q. H.; Li, C. (2009). "On the occurrence of the ichthyosaur Shastasaurus in the Guanling biota (Late Triassic), Guizhou, China". Vertebrata PalAsiatica 47 (3): 178–193.

Life restoration of the Triassic ichthyosaur Callawayia neoscapularis. Three specimens of this ichthyosaur are known, the holotype, ROM 41993, and two referred specimens, TMP 94.380.11 and 94.382.2. The skull is primarily based on ROM 41993, cross-checked against TMP 94.380.11 and TMP 94.382.2. The vertebral column is based primarily on TMP 94.382.2 as it is the most complete of these specimens, while the ribs were based on ROM 41993. The forelimbs were mainly based on those of ROM 41993, with TMP 94.380.11 used to determine their breadth. The hindlimbs were based on TMP 94.380.11, especially the more complete right hindlimb. ROM 41993 was cross-scaled with TMP 94.380.11 by the dimensions of the forelimb epipodials, which produced similar vertebral dimensions. The two TMP specimens were cross-scaled based on femoral length, also producing similar vertebral dimensions. Nicholls & Manabe (2001) stated that no wedge-shaped caudal centra supporting a tailbend were found and that there was no evidence of a bend being present, though considered that they might have existed in the gap in the preserved caudals. Since various other Triassic ichthyosaurs have since been found to have tail bends, one was illustrated here. A modest downturn of roughly 15° was illustrated, comparable to that in Guanlingsaurus, and the location of the bend within the gap in the preserved vertebrae matches well with the location of the bend in Guizhouichthyosaurus. References McGowan, C. (1994). "A new species of Shastasaurus (Reptilia: Ichthyosauria) from the Triassic of British Columbia: The most complete exemplar of the genus". Journal of Vertebrate Paleontology 14 (2): 168–179. DOI:10.1080/02724634.1994.10011550. Nicholls, E. L.; Manabe, M. (2001). "A new genus of ichthyosaur from the Late Triassic Pardonet Formation of British Columbia: Bridging the Triassic-Jurassic gap". Canadian Journal of Earth Sciences 38 (6): 983–1002. Ji, C.; Jiang, D.Y.; Hao, W.; Sun, Y. (2011). "True tailbend occurred in the Late Triassic: Evidence from ichthyosaur skeletons of South China". Acta Scientiarum Naturalium Universitatis Pekinensis 47 (2): 309–314. Shang, Q. H.; Li, C. (2009). "On the occurrence of the ichthyosaur Shastasaurus in the Guanling biota (Late Triassic), Guizhou, China". Vertebrata PalAsiatica 47 (3): 178–193.

China Jurassic Late Triassic Triassic +12
Megacephalosaurus eulerti reconstructed skull in the Rocky Mountain Dinosaur Resource Center, Woodland Park, Colorado.

Megacephalosaurus eulerti reconstructed skull in the Rocky Mountain Dinosaur Resource Center, Woodland Park, Colorado.

Dinosauria Megacephalosaurus skull
Holotype skull of the centrosaurine ceratopsian dinosaur Diabloceratops eatoni from the Late Cretaceous (Campanian) of the Wahweap Formation, Grand Staircase-Escalante National Monument, Utah. Photograph by Nick Longrich, 2023.

Holotype skull of the centrosaurine ceratopsian dinosaur Diabloceratops eatoni from the Late Cretaceous (Campanian) of the Wahweap Formation, Grand Staircase-Escalante National Monument, Utah. Photograph by Nick Longrich, 2023.

Campanian Cretaceous Late Cretaceous holotype +5
Diagram of the skull of Haya griva in lateral view, reconstructed from IGM 100/2017

Diagram of the skull of Haya griva in lateral view, reconstructed from IGM 100/2017

Haya skull
Reconstructions of diplodocoid skulls used in this analysis.

Reconstructions of Nigersaurus and Diplodocus modified from [10] and [34], respectively. All other reconstructions based on material listed in Table S1. Skulls scaled to equivalent anteroposterior lengths.

Reconstructions of diplodocoid skulls used in this analysis. Reconstructions of Nigersaurus and Diplodocus modified from [10] and [34], respectively. All other reconstructions based on material listed in Table S1. Skulls scaled to equivalent anteroposterior lengths.

Diplodocia Nigersaurus Suuwassea skull
Skull of Yulong mini. The horizontal line projected through the posterodorsal corner of the antorbital fenestra is parallel to the line linking the articular end of the quadrate and the ventral margin of the premaxillae.

Skull of Yulong mini. The horizontal line projected through the posterodorsal corner of the antorbital fenestra is parallel to the line linking the articular end of the quadrate and the ventral margin of the premaxillae.

Yulong skull
The palatal view of the skull of NMS G.2021.6.2 and comparative assessment of the pterygoid region. The palatal region of NMS G.2021.6.2, A as seen in the ventral view. The comparative, to scale, pterosaur palatine and palatal regions in the ventral view. From left to right: B Cacibupteryx (IGO-V 208); C Parapsicephalus (GSM 3166); D Dearc (NMS G.2021.6.2); E Rhamphorhynchus (NHM R 2786); F Rhamphorhynchus (CM 11434). Abbreviations: bsp—basipterygoid; cho—choana; ec -, ectopterygoid; ipv—interpterygoid vacuity; pal—palatine; pf—posterior palatine fenestra; pte—pterygoid; stf -subtemporal fenestra; sof – suborbital fenestra; vm—vomer. Scale bar 10 mm

The palatal view of the skull of NMS G.2021.6.2 and comparative assessment of the pterygoid region. The palatal region of NMS G.2021.6.2, A as seen in the ventral view. The comparative, to scale, pterosaur palatine and palatal regions in the ventral view. From left to right: B Cacibupteryx (IGO-V 208); C Parapsicephalus (GSM 3166); D Dearc (NMS G.2021.6.2); E Rhamphorhynchus (NHM R 2786); F Rhamphorhynchus (CM 11434). Abbreviations: bsp—basipterygoid; cho—choana; ec -, ectopterygoid; ipv—interpterygoid vacuity; pal—palatine; pf—posterior palatine fenestra; pte—pterygoid; stf -subtemporal fenestra; sof – suborbital fenestra; vm—vomer. Scale bar 10 mm

scale Cacibupteryx Dearc Parapsicephalus +3
a Skeletal reconstruction of A. greppini. Elements preserved in the material and therefore providing information for the skeletal reconstruction are marked in blue. Because much information is missing from the incomplete skeletal material, the dorsal vertebrae, the proportions and morphology of the cervical vertebrae and the skull were modified from Camarasaurus. b Scaled silhouette drawings of Cetiosauriscus stewarti (in black) and A. greppini (in grey) demonstrating the significant size difference between the two taxa. Scale bar is 1 m

a Skeletal reconstruction of A. greppini. Elements preserved in the material and therefore providing information for the skeletal reconstruction are marked in blue. Because much information is missing from the incomplete skeletal material, the dorsal vertebrae, the proportions and morphology of the cervical vertebrae and the skull were modified from Camarasaurus. b Scaled silhouette drawings of Cetiosauriscus stewarti (in black) and A. greppini (in grey) demonstrating the significant size difference between the two taxa. Scale bar is 1 m

scale drawing Amanzia Camarasaurus +2
Fossil samples – e.g. ‘primitive’ bony fish (1, 2), a skull of a temnospondyl ‘amphibian’ (probably a metoposauroid) in dorsal view (3), a skull of an archosaur of the crocodile lineage (probably a phytosaur) in palatal view (4), holotype of the “gliding reptile” Icarosaurus siefkeri [1] (5) and Atreipus-Grallator-type dinosaur tracks (bottom right) – from the Newark Supergroup, i.e. a series of mainly Late Triassic to Early Jurassic sedimentary rocks of eastern North America


↑ Edwin H. Colbert: A gliding reptile from the Triassic of New Jersey. American Museum Novitates, 2230. American Museum of Natural History, New York 1966, digitallibrary.amnh.org, cf. fig. 3 therein.

Fossil samples – e.g. ‘primitive’ bony fish (1, 2), a skull of a temnospondyl ‘amphibian’ (probably a metoposauroid) in dorsal view (3), a skull of an archosaur of the crocodile lineage (probably a phytosaur) in palatal view (4), holotype of the “gliding reptile” Icarosaurus siefkeri [1] (5) and Atreipus-Grallator-type dinosaur tracks (bottom right) – from the Newark Supergroup, i.e. a series of mainly Late Triassic to Early Jurassic sedimentary rocks of eastern North America ↑ Edwin H. Colbert: A gliding reptile from the Triassic of New Jersey. American Museum Novitates, 2230. American Museum of Natural History, New York 1966, digitallibrary.amnh.org, cf. fig. 3 therein.

museum Early Jurassic Jurassic Late Triassic +8
Representative taxa from the Santonian Iharkút fauna from the Csehbánya Formation, Bakony Mountains, western Hungary. A Pannoniasaurus inexpectatus (Squamata, Mosasauroidea), dorsal vertebra (MTM uncatalogued) in dorsal view (photo by Réka Kalmár) B Foxemys trabanti (Pleurodira, Bothremydidae), skull (MTM V 2010.215.1.) in dorsal view (photo by Márton Rabi). C Bicuspidon aff. hatzegiensis (Squamata, Borioteiioidea), left dentary (MTM 2006.112.1.) in medial view (photo by László Makádi) D Basal tetanuran (Theropoda, Tetanurae), tooth (MTM V.01.54) in ?lingual view E Indeterminate abelisaurid (Theropoda, Abelisauridae), pedal ungual phalanx (MTM V 2008.43.1.) in lateral view F Pneumatoraptor fodori (Theropoda, Paraves), left scapulocoracoid (holotype, MTM V 2008.38.1.) in lateral view G Mochlodon vorosi (Ornithopoda, Rhabdodontidae), left dentary (holotype, MTM V 2010.105.1) in lateral view H Bakonydraco galaczi (Pterosauria, Azhdarchidae), mandible (holotype, MTM 2007.110.1) in dorsal view I Iharkutosuchus makadii (Eusuchia, Hylaeochampsidae), skull (holotype, MTM 2006.52.1) in dorsal view J Hungarosaurus tormai (Ankylosauria, Nodosauridae), right dentary (MTM 2007.25.2) in lateral view K Bauxitornis mindszentyae (Aves, Enantiornithes), left tarsometatarsus (holotype, MTM V 2009.38.1) in anterior view L Ajkaceratops kozmai (Ceratopsia), fused rostral and premaxillae (holotype, MTM V 2009.192.1) in lateral view. Scale bars: 2 cm in A, V, G, H, I, J; 1 cm in D, E, F, K, L; 1 mm in C.

Representative taxa from the Santonian Iharkút fauna from the Csehbánya Formation, Bakony Mountains, western Hungary. A Pannoniasaurus inexpectatus (Squamata, Mosasauroidea), dorsal vertebra (MTM uncatalogued) in dorsal view (photo by Réka Kalmár) B Foxemys trabanti (Pleurodira, Bothremydidae), skull (MTM V 2010.215.1.) in dorsal view (photo by Márton Rabi). C Bicuspidon aff. hatzegiensis (Squamata, Borioteiioidea), left dentary (MTM 2006.112.1.) in medial view (photo by László Makádi) D Basal tetanuran (Theropoda, Tetanurae), tooth (MTM V.01.54) in ?lingual view E Indeterminate abelisaurid (Theropoda, Abelisauridae), pedal ungual phalanx (MTM V 2008.43.1.) in lateral view F Pneumatoraptor fodori (Theropoda, Paraves), left scapulocoracoid (holotype, MTM V 2008.38.1.) in lateral view G Mochlodon vorosi (Ornithopoda, Rhabdodontidae), left dentary (holotype, MTM V 2010.105.1) in lateral view H Bakonydraco galaczi (Pterosauria, Azhdarchidae), mandible (holotype, MTM 2007.110.1) in dorsal view I Iharkutosuchus makadii (Eusuchia, Hylaeochampsidae), skull (holotype, MTM 2006.52.1) in dorsal view J Hungarosaurus tormai (Ankylosauria, Nodosauridae), right dentary (MTM 2007.25.2) in lateral view K Bauxitornis mindszentyae (Aves, Enantiornithes), left tarsometatarsus (holotype, MTM V 2009.38.1) in anterior view L Ajkaceratops kozmai (Ceratopsia), fused rostral and premaxillae (holotype, MTM V 2009.192.1) in lateral view. Scale bars: 2 cm in A, V, G, H, I, J; 1 cm in D, E, F, K, L; 1 mm in C.

tooth vertebra Hungary Santonian +15
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News

Paleontologists Identify New Species of Glyptodont
Paleontologists Identify New Species of Glyptodont
museum Denmark new species skull
An incomplete fossilized skull that has sat in the collections of the Natural History Museum of Denmark since the 19th century has turned out to represent a previously unrecognized species of glyptodont (genus Glyptotherium) that once roamed South America. The post Paleontologists Identify New Species of Glyptodont appeared first on Sci.News: Breaking Science News.
28/08/2026 sci-news
Remarkable New Museum für Naturkunde Berlin Galleries Open to Visitors
museum skull
Two remarkable Museum für Naturkunde Berlin galleries are being opened to visitors for the first time. The new "Mammal Skulls" and "Deer and Horned Animals" galleries will welcome members of the public during the Long Night of Museums event on Saturday 29th of August. Until now, these collections have been reserved exclusively for researchers. Their
28/08/2026 everythingdinosaur
Meet Bataspis crux, Jawless Fish that Cruised Devonian Seas with Batwing Head
Meet Bataspis crux, Jawless Fish that Cruised Devonian Seas with Batwing Head
jaw China Devonian Late Devonian fish new species skull
Paleontologists in China have identified a new species of armored, jawless fish from rocks around 419 million years old whose skull was shaped like the wing of a bat and whose unusual head made it an efficient glider through Devonian seas. The post Meet Bataspis crux, Jawless Fish that Cruised Devonian Seas with Batwing Head appeared first on Sci.News: Breaking Science News.
18/08/2026 sci-news
A 30-year-old fossil was hiding bones from a mysterious ancient sea monster
bone jaw Cretaceous fossil Mosasaurus new species skull
Fossils collected in Osaka more than 30 years ago have revealed a surprise hiding in plain sight: four previously unrecognized bones from a giant Cretaceous mosasaur. Among them is the first confirmed premaxilla—the frontmost bone of the upper jaw—ever identified in a Japanese mosasaur fossil. Even more intriguing, parts of the skull show unusual anatomical features that don’t match known mosasaurs, raising the possibility that the remains belong to an entirely new species.
15/08/2026 sciencedaily
A New Genus of Troodontid Dinosaur from New Mexico
bone Mexico Campanian Cretaceous Late Cretaceous fossil Dinevenator Dinosauria Troodontidae new species skull
Palaeontologists have named a new species of theropod dinosaur from New Mexico. The dinosaur, Dinevenator robustus, lived around 73 million years ago (Campanian faunal stage of the Late Cretaceous). Researchers identified the dinosaur from a fossil skull bone (a frontal) found in north-western New Mexico. It represents a new genus and species of troodontid. Troodontids
13/08/2026 everythingdinosaur
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