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Ornithocheiridae

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Ornithocheirids
Temporal range: Valanginian-Cenomanian,
~140–96 Ma
Restored skeleton of Tropeognathus mesembrinus in the National Museum of Brazil
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Order: †Pterosauria
Suborder: †Pterodactyloidea
Clade: †Ornithocheiriformes
Clade: †Ornithocheirae
Family: †Ornithocheiridae
Seeley, 1870
Type species
†Pterodactylus simus
Owen, 1861
Genera
Synonyms

Ornithocheiridae (or ornithocheirids, meaning "bird hands") is a group of pterosaurs within the suborder Pterodactyloidea. These pterosaurs were among the last to possess teeth. Members that belong to this group lived from the Early to Late Cretaceous periods (Valanginian to Cenomanian stages), around 140 to 96 million years ago.

Ornithocheirids are generally infamous for having an enormously controversial and very confusing taxonomy. Although agreements that these animals were related, and therefore similar to istiodactylids and pteranodontians, there is still no virtual consensus over the exact content and interrelationships of this group.[1] Ornithocheirids were the most successful pterosaurs during their reign, they were also the largest pterosaurs before the appearance of the azhdarchids such as Quetzalcoatlus. Ornithocheirids were excellent fish hunters, they used various flight techniques to catch their prey, and they are also capable of flying great distances without flapping constantly. The later existence of the crested pteranodontids made paleontologists think that ornithocheirids were their potential ancestors. This is due to their very similar aspects such as the different flying techniques, the long distance flights, and most of all their diet, which consists mainly on fish.

History

Naming

Holotype specimens of Ornithocheirus simus (A to D) and junior synonym O. platyrhinus (E to H)

The family Ornithocheiridae is without a doubt, one of the most well-known pterosaur groups, this is mostly due to their very controversial and convoluted taxonomic history. Most of the ornithocheirid fossil record consists of isolated teeth, as well as fragmentary bones, reaching hundreds or even thousands of remains in some localities.[1] The first uncovered ornithocheirid remains were described in 1861 by British paleontologist Sir Richard Owen; he assigned the fossil remains to a new species of Pterodactylus: P. simus.[2] In 1869, British paleontologist Harry Govier Seeley erected the new generic name Ornithocheirus (from Ancient Greek meaning "bird hand"), and assigned P. simus as its type species, therefore creating Ornithocheirus simus. Later, in 1870, Seeley created the name Ornithocheirae to only contain Ornithocheirus.[3] However, in the same year, this was emended to Ornithocheiridae by Seeley himself following the article 11.7.1.3 of the ICZN.[4] In 1874, Owen had proposed two new genera for the Cretaceous British pterosaurs: Coloborhynchus (meaning "maimed beak") and Criorhynchus (meaning "ram beak") based on highly distinctive jaw fragments.[5] Owen reassigned P. simus as the type species of Criorhynchus, creating Criorhynchus simus. He referred three species to Coloborhynchus, including the addition of a new species called C. clavirostris; no type species was designated however.[6] In 1876 however, Seeley pointed out that Criorhynchus was a junior synonym of Ornithocheirus, a concept that was followed by paleontologist Richard Lydekker in 1888.[5] In the latter year, Lydekker acknowledged that Ornithocheirus simus was the type species of Ornithocheirus, he also distinguished O. simus by its tall rostrum, while other species referred to Ornithocheirus had lanceolate jaw tips. Therefore, to avoid confusion, Lydekker preferred to use the name Criorhynchus for O. simus, and Ornithocheirus for the species with lanceolate jaw tips, this concept was later favored by paleontologist Reginald Walter Hooley in 1914. In his review of Ornithocheirus, he divided the family Ornithocheiridae into two subfamilies: Ornithocheirinae and Criorhynchinae; the former consisted of Ornithocheirus and Lonchodectes, while the latter consisted of Amblydectes and Criorhynchus.[7] In his review, Hooley also considered the species Coloborhynchus clavirostris as a synonym of Criorhynchus simus.[4][8] In 1967, paleontologist Oskar Kuhn placed Criorhynchus within the family Criorhynchidae (which is a term now considered synonymous to Ornithocheiridae), and also recognized Ornithocheirus within the family Ornithocheiridae and subfamily Ornithocheirinae. He also designated the species Coloborhynchus clavirostris as the type species of Coloborhynchus, but agreed with Hooley that it was synonymous with Criorhynchus simus.[6][4] In 1994 however, Yuong-Nam Lee revalidated the genus Coloborhynchus (with C. clavirostris as its type species), and regarded it as distinct from Criorhynchus simus.[6] Later, in 2001, paleontologist David Unwin revised the taxonomic history of the Cambridge Greensand pterosaurs, and divided Ornithocheiridae into three genera: Ornithocheirus, Coloborhynchus and Anhanguera. Unwin also designated Pterodactylus simus as the type and only species of Ornithocheirus.[4]

In 2003, Unwin defined the family Ornithocheiridae as Haopterus gracilis, Ornithocheirus simus, their most recent common ancestor, and all its descendants. He included the genera Anhanguera, Brasileodactylus, Coloborhynchus, Haopterus, Ludodactylus and Ornithocheirus within the family, and also concluded that Araripesaurus, Arthurdactylus and Santanadactylus may belong to this family as well. However, their taxonomic status and precise relationships with other ornithocheirids are uncertain.[9] In 2019, upon the description of the pterosaur Mimodactylus, Haopterus, which was assigned to this family by Unwin,[9] and recovered as a basal eupterodactyloid by Brian Andres and colleagues,[10] was reassigned by Alexander Kellner and colleagues as the sister taxon of the former.[11]

In 2014, Andres and colleagues defined the Ornithocheiridae with a different definition: the most inclusive clade containing Ornithocheirus simus but not Anhanguera blittersdorffi. They placed the genera Coloborhynchus, Ornithocheirus and Tropeognathus within the Ornithocheiridae, while placing Anhanguera within the separate family Anhangueridae.[10] However, back in 2001, Unwin considered the name Anhangueridae a junior synonym of Ornithocheiridae,[5] a concept that was later followed by several paleontologists such as Mark Witton in 2013.[1] Some phylogenetic analyses however, contradict this name synonymy, with Ornithocheiridae and Anhangueridae classified as different families, therefore following the 2014 analysis by Andres and colleagues instead.[12][13][14] Other studies such as the ones by Kellner and colleagues in 2019 have used a different concept, classifying Coloborhynchus, Tropeognathus, as well as several other close relatives such as Ludodactylus and Caulkicephalus within the Anhangueridae, which, along with the family Hamipteridae, forms the larger group Anhangueria. They assigned Ornithocheirus outside the Anhangueria due to being undiagnosable.[4][11][15] A lot of recent studies have since then followed this concept.[16][17][18]

Description

Comparison between the holotypes of Ornithocheirus (A and C) and Tropeognathus (B and D)

Among toothed pterodactyloids, ornithocheirids were the largest;[19] they were also among the most successful and widely distributed pterosaurs. Ornithocheirids were characterized by long jaws that had spike-like teeth. Ornithocheirid wingspans varied in size, with smaller species having wigspans of approximately 4 meters (13 ft), while giant morphs reached wingspans of up to 8 meters (26 ft) or more.[13] Specimen NHMUK R481, a specimen that belongs to the species Coloborhynchus capito, the largest toothed pterosaur, had wingspan that may have reached 7 meters (23 ft).[20] However, in 2013, a specimen referred to the genus Tropeognathus (MN 6594-V), a possible ornithocheirid (because it may also be anhanguerid),[21] was calculated to have had a normal wingspan of 8.26 meters (27.1 ft), while a calculated maximum wingspan reached 8.70 meters (28.5 ft), meaning that this specimen clearly shows that wingspans of toothed pterosaurs could exceed 7 meters (23 ft).[21]

Skull

Skull comparisons between different anhanguerians, notice the ornithocheirids Caulkicephalus (D), Tropeognathus (E and F) and Uktenadactylus (I and J)

Ornithocheirids had elongated jaws with rounded sagittal crests on both tips, as well as robust fang-like teeth.[13][22] The sagittal crest of the species Ornithocheirus simus and Tropeognathus mesembrinus extended to the anterior end of the rostrum, a feature that is also seen in the ornithocheirid (or alternately anhanguerid)[18] species Siroccopteryx moroccensis; further synapomorphies between these three species were also found, including the premaxilla having a tall and narrow shape in anterior aspect, the anterolateral margins of the premaxilla being convex in both anterior and lateral view, a feature that resulted in a bluntly rounded outline of the tip of the rostrum. The rostrum in S. moroccensis lacks a constriction that is posterior to the anterior rosette, a feature also shared by O. simus and T. mesembrinus, therefore another synapomorphy supported by these three species. Yet another feature shared by these three species is that the teeth are short, straight, and relatively uniform in size, something that is not present in other ornithocheirans such as Coloborhynchus and Anhanguera.[13] In Coloborhynchus, the teeth were found to have been heterodont, elongated, recurved and caniniform, which is similar to those seen in another ornithocheirid (though also recovered as an anhanguerid)[16][18] called Caulkicephalus.[23] The genus Caulkicephalus, though having similarities with other ornithocheirids, including the anterior end of the rostrum being transversely expanded, or having a low, bony sagittal crest that includes a smooth dorsal margin on the rostrum, still possesses some unique features. The most distinct characteristic of Caulkicephalus is that it bores a frontoparietal crest, a feature that is only seen in pteranodontians such as Pteranodon, and in Ludodactylus,[24] a pterosaur once assigned to the Ornithocheiridae, but some recent analysis have placed it within the more inclusive group Anhangueria, outside the Ornithocheiridae.[12][14] Other studies however, have recovered it within the Anhangueridae instead.[16][11][18]

Postcranial skeleton

Restoration of three Tropeognathus in flight, notice their high aspect ratio

The forelimbs of ornithocheirids were proportionally enormous, around five times longer than their legs. Substantial anchorage on the body is required given the mighty arms, and accordingly, ornithocheirids have robust scapulocoracoids, and stout, deeply keeled sterna, which served the purpose of housing their substantial forelimb muscles. The shoulder or pectoral girdle in ornithocheirids is set at a perpendicular angle to the spine, with the coracoids being much longer than the scapulae. The shoulder girdle is also of typical construction for ornithocheiroids. Over 60 percent of the wing length is occupied by the wing fingers, making them among the longest possessed by any pterodactyloids.[25]

In adult ornithocheirids, the sacrum develops a supraneural plate above its neural spines. The tails of ornithocheirids are poorly known, though they appear to be composed of at least eleven short vertebrae, and become relatively circular in cross section toward the end of the series. Like the related istiodactylids, the slender femora of ornithocheirids have femoral heads that project almost in line with the femoral shaft, but seem to lack prominent processes that anchor their hindlimb muscles. Ornithocheirid shinbones (or tibiae) are similarly developed and of equal length to the femora. Although the feet in ornithocheirids are poorly known, they seem to be relatively small and gracile, with undeveloped claws and a hooklike fifth metatarsal.[26]

Classification

Holotype skull and mandible of the ornithocheirids Ferrodraco (A) and Mythunga (B), and holotype mandible of Aussiedraco (C)

The family Ornithocheiridae has had a controversial and very confusing taxonomic history; paleontologists who have studied this group seem to have had a different opinion on the composition of ornithocheirid taxonomy. A term called Anhangueridae was coined by Diogenes de Almeida Campos and Kellner in 1985 to refer to pterosaurs that belong in this family. In 2001 however, Unwin argued that the name Ornithocheiridae refers to an identical group, and should have nomenclatural priority.[1] He therefore considered Anhangueridae a junior synonym of Ornithocheiridae in his study of pterosaur phylogeny in 2003.[9] However, in many recent studies, Anhangueridae is recovered as a separate and distinct family from Ornithocheiridae, each containing different genera.[27] The original term Ornithocheirae by Seeley had been redefined as the least inclusive clade containing Anhanguera blittersdorffi and Ornithocheirus simus,[10] therefore it is recovered as a larger group comprising the families Anhangueridae and Ornithocheiridae in recent analysis.[10][12][13][14]

Formerly assigned genera

In the past, many pterosaur genera were assigned to the Ornithocheiridae, however, following recent studies, these supposed ornithocheirids had been reclassified to other groups or families. The pterosaur Boreopterus for example, was initially classified within the Ornithocheiridae, however, later analysis had found it in a different family called Boreopteridae, with Boreopterus being the sister taxon of Zhenyuanopterus; both pterosaurs were recovered as basal members of the Lanceodontia in several recent studies such as the ones by Rodrigo Pêgas and colleagues,[17] and Adele Pentland and colleagues, both studies of which are from 2019.[14]

Aetodactylus is another pterosaur that was initially classified within the Ornithocheiridae; later analysis have found it outside the Ornithocheiridae: Timothy Myers in 2015 and Nicholas Longrich and colleagues in 2018 for example, are two studies that found Aetodactylus as sister taxon to the two species of Cimoliopterus (C. cuvieri and C. dunni).[27][12] In 2019, Pêgas and colleagues have found Aetodactylus, along with two other pterosaurs (Camposipterus and Cimoliopterus), within the clade Targaryendraconia, more specifically placed within the family Cimoliopteridae in a polytomy.[17]

The genus Haopterus was used to define the Ornithocheiridae in Unwin's 2003 study, however, Andres and Myers in 2013 argued that Haopterus had not been previously referred to the Ornithocheiridae besides a note added in proof to Unwin in 2001 that stated that Haopterus appeared to be a small ornithocheirid. Phylogenetic analyses since then have found Haopterus as a rogue taxon either within the Pterodactyloidea, the Ornithocheiroidea, the Pteranodontoidea, or the Istiodactylidae. In the phylogenetic analysis by Andres and Myers, Haopterus was recovered as a stable sister taxon to the group Ornithocheiroidea.[28] Some later analyses have also recovered this concept, with both Haopterus and the Ornithocheiroidea placed within the larger group Eupterodactyloidea.[10][29][12] Another study in 2019 had recovered Haopterus within a different group called Mimodactylidae.[11]

Phylogeny

Different phylogenetic analysis have found Ornithocheiridae to comprise different genera, the most typical ones being Tropeognathus, Coloborhynchus and Ornithocheirus.[28][27] In 2014, Andres and colleagues created the subfamily Ornithocheirinae to contain Coloborhynchus and Ornithocheirus, this subfamily was sister taxon to Tropeognathus, and altogether formed the family Ornithocheiridae.[10] In 2018, Longrich and colleagues had included the genus Siroccopteryx in their phylogenetic analysis, specifically as a member of the ornithocheirine subfamily, sister taxon to Coloborhynchus.[12] In 2019, a study performed by Adele Pentland and colleagues had found the Ornithocheiridae to comprise more genera; while the typical Tropeognathus, Coloborhynchus and Ornithocheirus clade was included in their analysis, Pentland and colleagues have found the genera Ferrodraco and Mythunga to belong the Ornithocheiridae as well, specifically sister taxa within the Ornithocheirinae, closely related to Ornithocheirus.[14] In the same year, Megan Jacobs and colleagues have recovered a different set of relationships for ornithocheirids in their analysis. Within the family, three clades emerge: the first one consists of Ornithocheirus, Tropeognathus and Siroccopteryx, the second one comprises Uktenadactylus with several Coloborhynchus species, and the third one comprises Cimoliopterus and Camposipterus. The close relationship between Siroccopteryx, Ornithocheirus and Tropeognathus is supported by several synapomorphies, such the teeth being short, straight, and relatively uniform in size.[13] Several other recent studies such as the ones by Alexander Kellner and colleagues,[15][11] or the one by Rodrigo Pêgas and colleagues, both in 2019, have recovered Coloborhynchus, Siroccopteryx, Tropeognathus, and Uktenadactylus within the family Anhangueridae instead of the Ornithocheiridae.[17] In 2020, a study by Borja Holgado and Pêgas had also recovered both Ferrodraco and Mythunga within the Anhangueridae instead of this family.[18]

Cimoliopterus has generally been recovered outside the Ornithocheiridae; subsequent analyses have found it as sister taxon to Aetodactylus, as mentioned earlier.[27][12] Another possible position for Cimoliopterus is within the clade Targaryendraconia, again, closely related to Aetodactylus, and together with Camposipterus, the three formed the family Cimoliopteridae.[17] In the analysis by Jacobs and colleagues, the two Cimoliopterus species had been found as sister taxa to the three Camposipterus species (C. nasutus, C. colorhinus and C. segwickii), altogether formed an unnamed clade within the Ornithocheiridae. However, as noted by Jacobs and colleagues, support for some of these arrangements is relatively weak due to the limited number of characters that can be scored, and the levels of homoplasy are very high.[13]

Below are two cladograms showing the possible genera that are included within the ornithocheirid family. The cladogram to the left is a topology recovered by Jacobs and colleagues,[13] and the one to the right is a topology recovered by Pentland and colleagues.[14]

Paleobiology

Diet and feeding

Restoration of Cimoliopterus stealing prey from a Lonchodectes

Ornithocheirids are generally considered piscivorous animals, this is mainly because they seem to have been suited for flight over marine settings,[30] in fact, most ornithocheirids are known from lagoonal, coastal and marine deposits.[31] Although the manner in which ornithocheirids gathered their food has not been researched in detail, it is generally thought that members of this family either fed like modern-day skimmers, pushing their lower jaw through the water to snap up food upon impact, or fed by gleaning food from the water surface like some modern-day terns and frigatebirds. The skim-feeding hypothesis on ornithocheirids has been discounted in recent assessments of pterosaur skim-feeding, while dip-feeding is supported by a number of anatomical features. Elongated ornithocheirid rostra are ideal for reaching into the water to grab swimming creatures. The rostral crests of ornithocheirids would have worked well as stabilizers for the jaws tips while being plunged into the water. Large, forward-facing eyes and well-developed flocculi are ideal for dip-feeding as well, which permits effective spotting of prey as well as judgement of distances when striking at them, as such, it seems likely that at least several ornithocheirids were efficient dip feeders. Sedate foraging methods might have also been used when hunting, example of these methods are: reaching food while being alighted on the water surface, and shallow surface dives.[30]

Locomotion and flight

Similar to modern-day albatrosses, most ornithocheirids used a flight technique called "dynamic soaring", which consists of travelling long distances without flapping using the vertical gradient of wind speed near the ocean surface as an advantage, but the flight speed is moderate. Several studies showed that most ornithocheirids sprawled their limbs to a large degree, similar to crocodiles, while other studies however, conclude that ornithocheirids were generally quadrupedal. Yet other studies concluded that ornithocheirids held their limbs more or less vertically extended, similar to an avian- or mammal-like configuration.[32] Some studies in the later genera, show that ornithocheirids spend much of their time sea fishing, and as a result, they perhaps influenced the later pteranodontids with the same piscivorous diet, as well as their well developed flight techniques.[33][34] Analyses of limb proportions in the genus Anhanguera however, show that some ornithocheirids were consistent on hopping, but the later genera were suggested that they most likely walked on four limbs, which consists on their wing-fingers as the front limbs, and using their hind limbs to balance.[35]

Paleoecology

Ornithocheirids were a widespreaded type of pterosaurs, with many fossil remains found across the world.[22] The first true ornithocheirid specimens were uncovered in the Cambridge Greensand of England, these belong to the infamous genus Ornithocheirus, and dated back to the Albian stage of the Early Cretaceous.[5] Within the fossil site, several other pterosaurs were also found, these include the pterosaurs Amblydectes and Coloborhynchus,[6] the targaryendraconian Camposipterus, the lonchodraconid Lonchodraco,[4] and the azhdarchoid Ornithostoma.[36] The ornithischians Anoplosaurus, Acanthopholis,[37] and the dubious Eucercosaurus and Trachodon were also found within the formation.[38] Fossil remains of the sauropod Macrurosaurus were also present.[39] The bird Enaliornis,[40] as well as the ichthyosaurs Cetarthrosaurus, Platypterygius and Sisteronia were also found alongside the remains of ornithocheirids.[41]

Geological map of the Araripe Basin of Brazil, with the extent of the Santana Group shown in dark blue

A Lagerstätte called the Santana Group (sometimes known as the Santana Formation) in northeastern Brazil was found to contain a large number of pterosaur genera. The most diverse formation of the group is the Romualdo Formation, known for its wide variety of pterosaur remains.[42] The formation dates back around 111 to 108 million years ago, also during the Albian stage of the Early Cretaceous. The Romualdo Formation is found to contain a variety of ornithocheirids (or anhanguerids), including Tropeognathus,[21] Coloborhynchus[43] and Araripesaurus,[44] the targaryendraconian Barbosania[45] as well as close relatives such as Anhanguera and Maaradactylus were also found alongside.[46] The related Araripedactylus, Brasileodactylus,[47] Cearadactylus,[48] Santanadactylus[49] and Unwindia[50] were also present within the fossil site. Many other pterosaur were found within, these include the tapejarid Tapejara,[51] as well as the thalassodromids (or thalassodromines, depending on the author) Thalassodromeus[52] and Tupuxuara.[53] Other animals such the theropods Irritator,[54] Mirischia[55] and Santanaraptor, as well as the crocodylomorph Araripesuchus were also found.[56] Several turtle remains were found within the formation, with some specimens referring to the genera Santanachelys, Cearachelys and Araripemys,[57][58] and along with these, many fish remains were also found, these were assigned to the genera Brannerion, Rhinobatos, Rhacolepis, Tharrhias and Tribodus.[59]

Ornithocheirids were also partially distributed in North America, and several specimens that were found are thought to belong to the genus Uktenadactylus (originally Coloborhychus wadleighi).[60] This pterosaur was uncovered in the Paw Paw Formation of Texas, United States, which dated back to the Albian and Cenomanian stages. The formation includes several ankylosaurian dinosaurs such as Pawpawsaurus, Texasetes, and an indetermine nodosaurid.[61][62][63] Within the fossil site, several specimens of ammonoids were thought to belong to the genera Turrilites and Scaphites,[64] and along with these, shark remains of Leptostyrax were also found.[65]

See also

References

  1. ^ a b c d Witton 2013, p. 152.
  2. ^ Martill, D.M. (2010). "The early history of pterosaur discovery in Great Britain". Geological Society of London, Special Publications. 343 (1): 287–311. doi:10.1144/SP343.18. S2CID 130116778.
  3. ^ Seeley, H.G. (1870). "The Ornithosauria: an Elementary Study of the Bones of Pterodactyles". Cambridge: 113.
  4. ^ a b c d e f Rodrigues, T.; Kellner, A. (2013). "Taxonomic review of the Ornithocheirus complex (Pterosauria) from the Cretaceous of England". ZooKeys (308): 1–112. doi:10.3897/zookeys.308.5559. PMC 3689139. PMID 23794925.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  5. ^ a b c d Unwin, D.M. (2001). "An overview of the pterosaur assemblage from the Cambridge Greensand (Cretaceous) of Eastern England". Mitteilungen aus dem Museum für Naturkunde in Berlin, Geowissenschaftliche Reihe. 4: 189–221.
  6. ^ a b c d "Review of the pterodactyloid pterosaur Coloborhynchus". Flugsaurier: Pterosaur Papers in Honour of Peter Wellnhofer. Zitteliana B. 28: 219–228. 2008. {{cite journal}}: Unknown parameter |authors= ignored (help)
  7. ^ Kellner AWA, Tomida Y (2000) Description of a new species of Anhangueridae (Pterodactyloidea) with comments on the pterosaur fauna from the Santana Formation (Aptian-Albian), northeastern Brazil. National Science Museum Monographs 17: 1-135.
  8. ^ Hooley, Reginald Walter (1914). "On the Ornithosaurian genus Ornithocheirus, with a review of the specimens from the Cambridge Greensand in the Sedgwick Museum, Cambridge". Annals and Magazine of Natural History. 13 (78): 529–557. doi:10.1080/00222931408693521. ISSN 0374-5481.
  9. ^ a b c Unwin, D. M. (2003). "On the phylogeny and evolutionary history of pterosaurs". Geological Society, London, Special Publications. 217 (1): 139–190. Bibcode:2003GSLSP.217..139U. CiteSeerX 10.1.1.924.5957. doi:10.1144/GSL.SP.2003.217.01.11. S2CID 86710955.
  10. ^ a b c d e f Andres, B.; Clark, J.; Xu, X. (2014). "The Earliest Pterodactyloid and the Origin of the Group". Current Biology. 24 (9): 1011–6. doi:10.1016/j.cub.2014.03.030. PMID 24768054.
  11. ^ a b c d e Kellner, Alexander W. A.; Caldwell, Michael W.; Holgado, Borja; Vecchia, Fabio M. Dalla; Nohra, Roy; Sayão, Juliana M.; Currie, Philip J. (2019). "First complete pterosaur from the Afro-Arabian continent: insight into pterodactyloid diversity". Scientific Reports. 9 (1): 17875. doi:10.1038/s41598-019-54042-z. PMC 6884559. PMID 31784545.
  12. ^ a b c d e f g Longrich, N.R., Martill, D.M., and Andres, B. (2018). "Late Maastrichtian pterosaurs from North Africa and mass extinction of Pterosauria at the Cretaceous-Paleogene boundary." PLoS Biology, 16(3): e2001663. doi:10.1371/journal.pbio.2001663
  13. ^ a b c d e f g h i "A new species of Coloborhynchus (Pterosauria, Ornithocheiridae) from the mid-Cretaceous of North Africa" (PDF). Cretaceous Research. 95: 77–88. 2019. doi:10.1016/j.cretres.2018.10.018. {{cite journal}}: Unknown parameter |authors= ignored (help)
  14. ^ a b c d e f g Pentland, Adele H.; Poropat, Stephen F.; Tischler, Travis R.; Sloan, Trish; Elliott, Robert A.; Elliott, Harry A.; Elliott, Judy A.; Elliott, David A. (December 2019). "Ferrodraco lentoni gen. et sp. nov., a new ornithocheirid pterosaur from the Winton Formation (Cenomanian–lower Turonian) of Queensland, Australia". Scientific Reports. 9 (1): 13454. doi:10.1038/s41598-019-49789-4. ISSN 2045-2322. PMC 6776501. PMID 31582757.
  15. ^ a b Kellner, Alexander W. A.; Weinschütz, Luiz C.; Holgado, Borja; Bantim, Renan A. M.; Sayão, Juliana M. (19 August 2019). "A new toothless pterosaur (Pterodactyloidea) from Southern Brazil with insights into the paleoecology of a Cretaceous desert". Anais da Academia Brasileira de Ciências. 91 (suppl 2): e20190768. doi:10.1590/0001-3765201920190768. ISSN 0001-3765. PMID 31432888.
  16. ^ a b c Borja Holgado, Rodrigo V. Pêgas, José Ignacio Canudo, Josep Fortuny, Taissa Rodrigues, Julio Company & Alexander W.A. Kellner, 2019, "On a new crested pterodactyloid from the Early Cretaceous of the Iberian Peninsula and the radiation of the clade Anhangueria", Scientific Reports 9: 4940 doi:10.1038/s41598-019-41280-4
  17. ^ a b c d e Rodrigo V. Pêgas, Borja Holgado & Maria Eduarda C. Leal (2019) On Targaryendraco wiedenrothi gen. nov. (Pterodactyloidea, Pteranodontoidea, Lanceodontia) and recognition of a new cosmopolitan lineage of Cretaceous toothed pterodactyloids, Historical Biology, doi:10.1080/08912963.2019.1690482
  18. ^ a b c d e Holgado, B.; Pêgas, R.V. (2020). "A taxonomic and phylogenetic review of the anhanguerid pterosaur group Coloborhynchinae and the new clade Tropeognathinae". Acta Palaeontologica Polonica. 65. doi:10.4202/app.00751.2020.
  19. ^ Eberhard D. Frey; Wolfgang Stinnesbeck; David M. Martill; Héctor E. Rivera-Sylva; Héctor Porras Múzquiz (2020). "The geologically youngest remains of an ornithocheirid pterosaur from the late Cenomanian (Late Cretaceous) of northeastern Mexico with implications on the paleogeography and extinction of Late Cretaceous ornithocheirids". Palæovertebrata. 43 (1): e4. doi:10.18563/pv.43.1.e4.
  20. ^ Martill, D.M. and Unwin, D.M. (2011). "The world's largest toothed pterosaur, NHMUK R481, an incomplete rostrum of Coloborhynchus capito (Seeley 1870) from the Cambridge Greensand of England." Cretaceous Research, (advance online publication). doi:10.1016/j.cretres.2011.09.003
  21. ^ a b c Kellner, A. W. A.; Campos, D. A.; Sayão, J. M.; Saraiva, A. N. A. F.; Rodrigues, T.; Oliveira, G.; Cruz, L. A.; Costa, F. R.; Silva, H. P.; Ferreira, J. S. (2013). "The largest flying reptile from Gondwana: A new specimen of Tropeognathus cf. T. mesembrinus Wellnhofer, 1987 (Pterodactyloidea, Anhangueridae) and other large pterosaurs from the Romualdo Formation, Lower Cretaceous, Brazil". Anais da Academia Brasileira de Ciências. 85 (1): 113–135. doi:10.1590/S0001-37652013000100009. PMID 23538956.
  22. ^ a b Witton 2013, p. 155.
  23. ^ Martill, David M. (2015), First occurrence of the pterosaur Coloborhynchus (Pterosauria, Ornithocheiridae) from the Wessex Formation (Lower Cretaceous) of the Isle of Wight, England., 126, vol. 3, Proceedings of the Geologists' Association, pp. 377–380, CiteSeerX 10.1.1.1064.6403
  24. ^ Steel, L., Martill, D.M., Unwin, D.M. and Winch, J. D. (2005). "A new pterodactyloid pterosaur from the Wessex Formation (Lower Cretaceous) of the Isle of Wight, England". Cretaceous Research. 26 (4): 686–698. doi:10.1016/j.cretres.2005.03.005.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  25. ^ Witton 2013, p. 159.
  26. ^ Witton 2013, pp. 159–160.
  27. ^ a b c d Myers, Timothy S. (2015). "First North American occurrence of the toothed pteranodontoid pterosaur Cimoliopterus". Journal of Vertebrate Paleontology. 35 (6): e1014904. doi:10.1080/02724634.2015.1014904. S2CID 86099117.
  28. ^ a b Andres, B.; Myers, T. S. (2013). "Lone Star Pterosaurs". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 103 (3–4): 1. doi:10.1017/S1755691013000303.
  29. ^ Upchurch, P.; Andres, B.B.; Butler, R.J.; Barrett, P.M. (2015). "An analysis of pterosaurian biogeography: implications for the evolutionary history and fossil record quality of the first flying vertebrates". Historical Biology. 27 (6): 697–717. doi:10.1080/08912963.2014.939077. PMC 4536946. PMID 26339122.
  30. ^ a b Witton 2013, p. 163.
  31. ^ "Pterosaur dietary hypotheses: a review of ideas and approaches". Biological Reviews. 93 (4): 2021–2048. 2018. doi:10.1111/brv.12431. PMC 6849529. PMID 29877021. {{cite journal}}: Unknown parameter |authors= ignored (help)
  32. ^ Witton 2013, p. 162.
  33. ^ Witton 2013, pp. 161–162.
  34. ^ Witton, M.P.; Habib, M.B. (2010). "On the Size and Flight Diversity of Giant Pterosaurs, the Use of Birds as Pterosaur Analogues and Comments on Pterosaur Flightlessness". PLOS ONE. 5 (11): e13982. Bibcode:2010PLoSO...513982W. doi:10.1371/journal.pone.0013982. PMC 2981443. PMID 21085624.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  35. ^ Habib, M. (2011). "Dinosaur Revolution: Anhanguera." H2VP: Paleobiomechanics. Weblog entry, 20-SEP-2011. Accessed 28-SEP-2011: http://h2vp.blogspot.com/2011/09/dinosaur-revolution-anhanguera.html
  36. ^ Averianov A.O. (2012). "Ornithostoma sedgwicki – valid taxon of azhdarchoid pterosaurs". Proceedings of the Zoological Institute RAS. 316 (1): 40–49.
  37. ^ Nopcsa, Baron Francis (1923). "Notes on the British dinosaurs, Part IV: Acanthopholis". Geological Magazine. 60 (5): 193–199. doi:10.1017/S0016756800085563.
  38. ^ Seeley, H. G. (1879). "On the Dinosauria of the Cambridge Greensand". Quarterly Journal of the Geological Society. 35 (1–4): 591–635. doi:10.1144/GSL.JGS.1879.035.01-04.42. S2CID 129277596.
  39. ^ H.G. Seeley, 1876, "On Macrurosaurus semnus (Seeley), a long tailed animal with procoelous vertebrae from the Cambridge Upper Greensand, preserved in the Woodwardian Museum of the University of Cambridge", Quarterly Journal of the Geological Society of London 32: 440-444 doi:10.1144/GSL.JGS.1876.032.01-04.50
  40. ^ Harrison, C.J.O.; Walker, C.A. (1973). "Wyleyia: a new bird humerus from the Lower Cretaceous of England" (PDF). Palaeontology. 16 (4): 721–728. Archived from the original (PDF) on 2012-02-06.
  41. ^ Valentin Fischer; Nathalie Bardet; Myette Guiomar & Pascal Godefroit (2014). "High Diversity in Cretaceous Ichthyosaurs from Europe Prior to Their Extinction". PLOS ONE. 9 (1): e84709. doi:10.1371/journal.pone.0084709. PMC 3897400. PMID 24465427.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  42. ^ Veldmeijer, A.J. (2006). "Toothed pterosaurs from the Santana Formation (Cretaceous; Aptian-Albian) of northeastern Brazil. A reappraisal on the basis of newly described material Archived 2012-03-17 at the Wayback Machine." Tekst. - Proefschrift Universiteit Utrecht.
  43. ^ Fastnacht, M (2001). "First record of Coloborhynchus (Pterosauria) from the Santana Formation (Lower Cretaceous) of the Chapada do Araripe of Brazil". Paläontologische Zeitschrift. 75: 23–36. doi:10.1007/bf03022595. S2CID 128410270.
  44. ^ "On the presence of a giant pterosaur in the Lower Cretaceous (Aptian) of Chapada do Araripe (northeastern Brazil)". Bollettino della Società Paleontologica Italiana. 32 (1): 131–136. 1993. {{cite journal}}: Unknown parameter |authors= ignored (help)
  45. ^ Ross A. Elgin & Eberhard Frey (2011). "A new ornithocheirid, Barbosania gracilirostris gen. et sp. nov. (Pterosauria, Pterodactyloidea) from the Santana Formation (Cretaceous) of NE Brazil". Swiss Journal of Palaeontology. 130 (2): 259–275. doi:10.1007/s13358-011-0017-4. S2CID 89178816.
  46. ^ Renan A. M. Bantim; Antônio A. F. Saraiva; Gustavo R. Oliveira; Juliana M. Sayão (2014). "A new toothed pterosaur (Pterodactyloidea: Anhangueridae) from the Early Cretaceous Romualdo Formation, NE Brazil". Zootaxa. 3869 (3): 201–223. doi:10.11646/zootaxa.3869.3.1. PMID 25283914.
  47. ^ "Description of Pterosaurian (Pterodactyloidea: Anhangueridae, Brasileodactylus) remains from the Lower Cretaceous of Brazil". Deinsea. 13: 9–40. 2009. {{cite journal}}: Unknown parameter |authors= ignored (help)
  48. ^ Leonardi, G. & Borgomanero, G. (1985). "Cearadactylus atrox nov. gen., nov. sp.: novo Pterosauria (Pterodactyloidea) da Chapada do Araripe, Ceara, Brasil." Resumos dos communicaçoes VIII Congresso bras. de Paleontologia e Stratigrafia, 27: 75–80.
  49. ^ P. H. Buisonjé. 1980. Santanadactylus brasilensis nov. gen., nov. sp., a long-necked, large pterosaurier from the Aptian of Brasil. Proceedings of the Koninklijke Nederlandse Akademie van Wetenschappen, B 83:145-172
  50. ^ Martill, David M. (2011). "A new pterodactyloid pterosaur from the Santana Formation (Cretaceous) of Brazil". Cretaceous Research. 32 (2): 236–243. doi:10.1016/j.cretres.2010.12.008.
  51. ^ Pinheiro, Felipe L.; Fortier, Daniel C.; Schultz, Cesar L.; De Andrade, José Artur F.G.; Bantim, Renan A.M. (2011). "New information on Tupandactylus imperator, with comments on the relationships of Tapejaridae (Pterosauria)". Acta Palaeontologica Polonica. 56 (3): 567–580. doi:10.4202/app.2010.0057.
  52. ^ Pêgas, R. V.; Costa, F. R.; Kellner, A. W. A. (2018). "New Information on the osteology and a taxonomic revision of The genus Thalassodromeus (Pterodactyloidea, Tapejaridae, Thalassodrominae)". Journal of Vertebrate Paleontology. 38 (2): e1443273. doi:10.1080/02724634.2018.1443273. S2CID 90477315.
  53. ^ Witton, Mark P. (October 2009). "A new species of Tupuxuara (Thalassodromidae, Azhdarchoidea) from the Lower Cretaceous Santana Formation of Brazil, with a note on the nomenclature of Thalassodromidae". Cretaceous Research. 30 (5): 1293–1300. doi:10.1016/j.cretres.2009.07.006.
  54. ^ Kellner, A.W.A.; Campos, D.A. (1996). "First Early Cretaceous theropod dinosaur from Brazil with comments on Spinosauridae". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 199 (2): 151–166. doi:10.1127/njgpa/199/1996/151.
  55. ^ Martill, D.M.; Cruickshank, A.R.I.; Frey, E.; Small, P.G.; Clarke, M. (1996). "A new crested maniraptoran dinosaur from the Santana Formation (Lower Cretaceous) of Brazil". Journal of the Geological Society. 153 (1): 5–8. Bibcode:1996JGSoc.153....5M. doi:10.1144/gsjgs.153.1.0005. S2CID 131339386.
  56. ^ Ortega, F. J.; Z. B. Gasparini; A. D. Buscalioni; J. O. Calvo (2000). "A new species of Araripesuchus (Crocodylomorpha, Mesoeucrocodylia) from the Lower Cretaceous of Patagonia (Argentina)". Journal of Vertebrate Paleontology. 20 (1): 57–76. doi:10.1671/0272-4634(2000)020[0057:ANSOAC]2.0.CO;2.
  57. ^ Zug, George R. "Turtle: Origin and evolution". Encyclopædia Britannica. Retrieved 18 September 2015.
  58. ^ Hirayama, Ren (1998-04-16). "Oldest known sea turtle". Nature. 392 (6677): 705–708. doi:10.1038/33669. S2CID 45417065.
  59. ^ Lane, Jennifer A.; Maisey, John G. (2012). "The Visceral Skeleton and Jaw Suspension In the Durophagous Hybodontid Shark Tribodus limae from the Lower Cretaceous of Brazil". Journal of Paleontology. 86 (5): 886–905. doi:10.1666/11-139.1. ISSN 0022-3360. S2CID 86285896.
  60. ^ Lee, Y.-N. (1994). "The Early Cretaceous Pterodactyloid Pterosaur Coloborhynchus wadleighi from North America". Palaeontology. 37 (4): 755–763.
  61. ^ Paulina-Carabajal, A.; Lee, Y.N.; Jacobs, L.L. (2016). "Endocranial Morphology of the Primitive Nodosaurid Dinosaur Pawpawsaurus campbelli from the Early Cretaceous of North America". PLOS ONE. 11 (3): e0150845. doi:10.1371/journal.pone.0150845. PMC 4805287. PMID 27007950.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  62. ^ Coombs, W. P. 1995. A nodosaurid ankylosaur (Dinosauria: Ornithischia) from the Lower Cretaceous of Texas. Journal of Vertebrate Paleontology 15(2):298-312. doi:10.1080/02724634.1995.10011231
  63. ^ Weishampel, David B; et al. (2004). "Dinosaur distribution (Early Cretaceous, North America)." In: Weishampel, David B.; Dodson, Peter; and Osmólska, Halszka (eds.): The Dinosauria, 2nd, Berkeley: University of California Press. Pp. 553-556. ISBN 0-520-24209-2.
  64. ^ William A.C. (1969). The Late Cretaceous Ammonites Scaphites leei Reeside and Scaphites hippocrepis (DeKay) in the Western Interior of the United States (PDF). United States Government Printing Office. pp. 3–7.
  65. ^ Cappetta H. 1987. Chondrichthyes II. Mesozoic and Cenozoic Elasmobranchii. Schultze H.-P. (ed.), Handbook of Paleoichthyology, Volume 3B. Gustav Fischer Verlag, Stuttgart, 193 p.

Further reading

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