Information about Pterosaur
- Pterodactyl redirects here. For the horror film, see Pterodactyl (film). For the aircraft designs see Westland-Hill Pterodactyl
| Pterosaurs Fossil range: Triassic – Cretaceous | ||||||||||
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| Scientific classification | ||||||||||
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Pterodactyloidea Rhamphorhynchoidea * | ||||||||||
Pterosaurs are sometimes referred to in the popular media as dinosaurs, but this is incorrect. The term "dinosaur" is properly restricted to a certain group of terrestrial reptiles with a unique upright stance (superorder Dinosauria), and therefore excludes the pterosaurs, as well as the various groups of extinct aquatic reptiles, such as ichthyosaurs, plesiosaurs, and mosasaurs.
History of discovery
Fossilised pterosaurs have been found in North America, South America, United Kingdom, Europe, Africa, Asia and Australia. The first pterosaur fossil was found by an Italian naturalist, Cosimo Collini, in 1784. The name "Ptero-dactyle" was first coined by Georges Cuvier in 1809 for a specimen recovered in Germany; however, due to the standardization of scientific names, the official name for this species became Pterodactylus, though the name "pterodactyl" continued to be popularly applied to all members of this first specimen's order.A famous UK find was an example of Dimorphodon by Mary Anning, at Lyme Regis in 1828.
At least 60 genera of pterosaurs have been found, ranging from the size of a small bird to wingspans in excess of 10 meters (33 feet). Since the first pterosaur fossil was discovered in the late Jurassic Solnhofen limestone in 1784, twenty-nine kinds of pterosaurs have been found in those deposits alone. Most paleontologists now believe that pterosaurs were adapted for active flight, not just gliding as was earlier believed.
The three dimensionally preserved skull of Anhanguera santanae, from the Santana Formation, Brazil.
Anatomy and palaeobiology
The anatomy of pterosaurs was highly modified from their reptilian ancestors for the demands of flight. Pterosaur bones were hollow and air filled, like the bones of birds. They had a keeled breastbone that was developed for the attachment of flight muscles and an enlarged brain that shows specialised features associated with flight.[2]Pteranodon skeletal drawing from a 1914 scientific paper.
Wings
Pterosaur wings were formed by membranes of skin and other tissues, strengthened by various types of closely spaced fibers.[3] The membranes attached to the extremely long fourth finger of each arm and extended along the sides of the body. A bone unique to pterosaurs, known as the pteroid, connected to the wrist and helped to support a membrane (the propatagium) between the wrist and shoulder. The pteroid might have been able to swing forward to extend this membrane,[4] although this is very debatable.[5][6] In some later pterosaurs, the backbone over the shoulders fused into a structure known as a notarium, which served to stiffen the torso during flight, and provide a stable support for the scapula (shoulder blade).There has been considerable argument among paleontologists about whether the wings attached to the hindlimbs as well. Fossils of the rhamphorhynchoid Sordes,[7] the anurognathid Jeholopterus,[8] and a pterodactyloid from the Santana Formation seem to demonstrate that the wing membrane did attach to the hindlimbs, at least in some species. However, modern bats and flying squirrels show considerable variation in the extent of their wing membranes and it is possible that, like these groups, different species of pterosaur had different wing designs. Indeed, analysis of pterosaur limb proportions shows that there was considerable variation, possibly reflecting a variety of wing-plans.[9] Many if not all pterosaurs also had webbed feet, and although these have been considered to be evidence of swimming, they may have had an aerodynamic function.[10]
Hair
There is no fossil evidence of feathers, but pterosaurs were unique among reptiles in that at least some of them were covered with hair, similar to but not homologous with mammalian hair. Pterosaur "hair" is not true hair as seen in mammals, but a unique structure that developed a similar appearance through convergent evolution. Although in some cases fibers in the wing membrane have been mistaken for hair, some fossils such as those of Sordes pilosus (the "hairy demon") do show the unmistakable imprints of hair on the head and body,<ref name="Unwin_Bakhurina_1994" /> not unlike modern-day bats, another example of convergent evolution. The presence of hair (and the demands of flight) imply that pterosaurs were warm-blooded ('endothermic').Nervous system
A study of pterosaur brain cavities using X-rays has revealed extraordinary information about their habits. Studying fossil pterosaur skulls is extremely difficult because they are so delicate, but Lawrence Witmer at Ohio University in Athens and his colleagues used X-ray CT scans to build up 3D images of the brains of two species.[2] One striking finding was that the animals (Rhamphorhynchus muensteri and Anhanguera santanae) had massive flocculi. The flocculus is a brain region that integrates signals from joints, muscles, skin and the balance organs.The pterosaurs' flocculi occupied 7.5% of the animals' total brain mass, more than in any other vertebrate. Birds have unusually large flocculi compared with other animals, but these only occupy between 1 and 2% of total brain mass.<ref name="Witmer_et_al_2003" />
The flocculus sends out neural signals that produce small, automatic movements in the eye muscles. These keep the image on an animal's retina steady. Pterosaurs may have had such a large flocculus because of their large wing size,<ref name="Witmer_et_al_2003" /> which would mean that there was a great deal more sensory information to process.
Ground movement
Pterosaur's hip sockets were oriented facing slightly upwards, and the head of the femur (thigh bone) was only moderately inward facing, suggesting that pterosaurs had a semi-erect stance. It would have been possible to lift the thigh into a horizontal position during flight.There has been considerable debate in the past about whether pterosaurs moved about on the ground as quadrupeds or as bipeds. A large number of pterosaur trackways are now known, with a distinctive four-toed hind foot and three-toed front foot; these are the unmistakable prints of pterosaurs walking on all fours.[11][12] It has been suggested that smaller pterosaurs with longer hindlimbs such as Dimorphodon might have walked or even run bipedally, in addition to flying, not unlike modern road runners. Other small pterosaurs such as Rhamphorhynchus may have scurried around on all fours. Larger pterosaurs with proportionately smaller hindlimbs and massive forebodies are generally thought to have moved about on all fours while on the ground.
Predation
Pterosaurs are known to have been eaten by spinosaurs. In the 1 July 2004 edition of Nature, paleontologist Eric Buffetaut discusses an early Cretaceous fossil of three cervical vertebrae of a pterosaur with the broken tooth of a spinosaur embedded in it. The vertebrae are known not to have been eaten and exposed to digestion, as the joints still articulated.[13]Reproduction
Very little is known about pterosaur reproduction. A single pterosaur egg has been found in the quarries of Liaoning, the same place that yielded the famous 'feathered' dinosaurs. The egg was squashed flat with no signs of cracking, so evidently the eggs had leathery shells.[14] The embryo's wing membranes were well developed,[15] suggesting pterosaurs were ready to fly soon after birth. This is corroborated by very young animals found in the Solnhofen limestone beds, where they presumably flew to the middle of a lagoon, fell in and drowned. It is not known whether pterosaurs practised parental care, but their comparatively early flight capabilities suggest the young were not completely dependent on parents as most birds are.A study of pterosaur eggshell structure and chemistry published in 2007 indicated that it is likely pterosaurs buried their eggs, like modern crocodile and turtles. Egg-buiring would have been beneficial to the early evolution of pterosaurs, as it allows for more weight-reducing adaptations, but this method of reproduction also would have put limits on the variety of environments pterosaurs could live in, and may have disadvantaged them when they began to face ecological competition from birds.[16]
Evolution and extinction
Origins
Because pterosaur anatomy has been so heavily modified for flight, and immediate "missing link" predecessors have not so far been described, the ancestry of pterosaurs is not well understood. They are generally, but not universally, thought to be related to the Dinosauria on the basis of their ankle structure.They are thought to have evolved flight from some manner other than the 'tree-down' route possibly taken by birds, because pterosaurs demonstrated no adaptations useful for tree living. Most scenarios have pterosaurs evolving from long-legged, ground-running ancestors like Scleromochlus or Sharovipteryx (a less likely scenario), both of which had webs of skin from long hind legs to their bodies or tails. This suggests a 'ground-up' evolution of flight or even a route that evolved by gliding from cliff-tops.
Phylogeny and classification
- For more details on this topic, see List of pterosaur classifications.
Classification of pterosaurs has historically been difficult, because there were many gaps in the fossil record. Many new discoveries are now filling in these gaps and giving us a better picture of the evolution of pterosaurs. Traditionally, they are organized into two suborders:
- Rhamphorhynchoidea (Plieninger, 1901): A group of early, basal ("primitive") pterosaurs, many of which had long tails and short metacarpal bones in the wing. They were small, and their fingers were still adapted to climbing . They appeared in the late Triassic period, and lasted until the late Jurassic. Rhamphorhynchoidea is a paraphyletic group (since the pterodactyloids evolved directly from them and not from a common ancestor), so with the increasing use of cladistics it has fallen out of favor in most technical literature.
- Pterodactyloidea (Plieninger, 1901): The more derived ("advanced") pterosaurs, with short tails and long wing metacarpals. They appeared in the middle Jurassic period, and lasted until the Cretaceous-Tertiary extinction event wiped them out at the end of the Cretaceous.

Rhamphorhynchus, a well-known "rhamphorhynchoid" from the Late Jurassic.

Zhejiangopterus, an azhdarchid from the Cretaceous of China.
- ORDER PTEROSAURIA (extinct)
- Suborder Rhamphorhynchoidea *
- Family Dimorphodontidae
- Family Anurognathidae
- Family Campylognathoididae
- Family Rhamphorhynchidae
- Suborder Pterodactyloidea
- Superfamily Ornithocheiroidea
- Family Istiodactylidae
- Family Ornithocheiridae
- Family Pteranodontidae
- Family Nyctosauridae
- Superfamily Ctenochasmatoidea
- Family Gallodactylidae
- Family Pterodactylidae
- Family Ctenochasmatidae
- Superfamily Dsungaripteroidea
- Family Germanodactylidae
- Family Dsungaripteridae
- Superfamily Azhdarchoidea
- Family Lonchodectidae
- Family Tapejaridae
- Family Azhdarchidae
| Pterosauria |
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Extinction
It is believed by some that competition with early bird species may have resulted in the extinction of many of the pterosaurs. By the end of the Cretaceous, only large species of pterosaurs are known. The smaller species seem to have become extinct, their niche filled by birds,[19] though a lack of small pterosaurs in the fossil record could also be a result of poor preservation due to the fragility of their skeletons. At the end of the Cretaceous period, the great extinction which wiped out all dinosaurs, and many other animals, seemed to also take the pterosaurs. Others suggest that most pterosaurs were specialised for an ocean-going lifestyle. Consequently, when the K-T mass-extinction severely affected marine life that most pterosaurs fed on, they went extinct.Well-known genera
- Dsungaripterus had a wingspan of 3 metres (10 feet), an unusual bony crest running along its snout, and long, narrow, curved jaws with a pointed tip. It lived during the early Cretaceous period.
- Pteranodon was 1.8 metres (six feet) long, with a wingspan of 7.5 m (25 feet), and lived during the late Cretaceous period.
- Pterodactylus had a wingspan of 50 to 75 centimeters (20 to 30 inches), and lived during the late Jurassic on lake shores.
- Pterodaustro was a Cretaceous pterosaur from South America with a wingspan around 1.33 metres and with over 500 tall, narrow teeth, which were presumably used in filter-feeding, much like modern flamingos. Also like flamingos, this pterosaur's diet may have resulted in the animal having a pink hue. It was South America's first pterosaur find.
- Quetzalcoatlus had a wingspan of 10-11 metres (33-36 feet), and was among the largest flying animal ever. It lived during the late Cretaceous period.
- Rhamphorhynchus was a Jurassic pterosaur with a vane at the end of its tail, which may have acted to stabilise the tail in flight.
Pterosaurs in popular culture
Pterosaurs are a staple of popular culture. While the generic term "pterodactyl" is often used to describe these creatures, the animal depicted is frequently a Pteranodon or other specific species of pterosaur, or a fictionalized hybrid of several species. Many childrens toys and cartoons feature "pterodactyls" with Pteranodon-like crests and long, Rhamphorhynchus-like tails and teeth, a combination that never existed in nature. However, at least one type of pterosaur did have at least the Pteranodon-like crest and teeth--the Ludodactylus, a name that means "toy finger" for its resemblance to old, inaccurate children's toys. Notable examples of older fictional works featuring pterosaurs include Arthur Conan Doyle's book The Lost World and the 1933 film King Kong.Living Pterosaur hoax
It was reported in an article in The Illustrated London News (February 9, 1856, page 166) that, in 1856, workmen laboring in a tunnel for a railway line, between Saint-Dizier and Nancy, in France, were cutting through Jurassic limestone when a large creature stumbled out from inside it. It fluttered its wings, made a croaking noise and dropped dead. According to the workers, the creature had a 10 foot wingspan, four legs joined by a membrane, black leathery skin, talons for feet and a toothed mouth. A local student of paleontology identified the animal as a pterodactyl. The report had the animal turn to dust, as soon as it had died.This incredible story is believed to have been a hoax, stimulated in part by contemporary Franco-Prussian palaeontological rivalry. The Solnhofen limestone from Bavaria (in which Archaeopteryx would later be discovered) was producing many prized fossils, each of which was proudly announced by German paleontologists. The tunnel in question was through limestone of similar age to the Solnhofen Limestone, so it presented an opportunity for a shocking story by the French.
Further reading
- Unwin, David M. (2006). Pterosaurs From Deep Time. Pi Press: New York. ISBN 0-13-146308-X
- Wellnhofer P (1991): Illustrated Encyclopedia of Pterosaurs, Crescent Books
Notes and references
1. ^ Another, name 'Ornithosauria' ('bird-lizard', Bonaparte 1838) was sometimes used in the earlier literature [1]
2. ^ Witmer W.M., Chatterjee, S., Franzosa, J. and Rowe, T. 2003. Neuroanatomy of flying reptiles and implications for flight, posture and behaviour. Nature 425, 950-953
3. ^ Bennett, S.C., 2000. Pterosaur flight: the role of actinofibrils in wing function. Historical Biology, 14:255-284.
4. ^ Wilkinson, M.T., Unwin, D.M. and Ellington, C.P., 2006. High lift function of the pteroid bone and forewing of pterosaurs, Proc Biol Sci. 273:1582 119-126 doi 10.1098/rspb.2005.3278
5. ^ Bennett, S.C., 2006 [Abstract] Articulation and function of the pteroid bone of pterosaurs. Journal of Vertebrate Paleontology, 26(Suppl. to #3):41A.
6. ^ Bennett, S.C. (2007). Reward for a Pteroid Errant. fhsu.edu/biology/cbennett/.
7. ^ Unwin, D.M. and Bakhurina, N.N., 1994. Sordes pilosus and the nature of the pterosaur flight apparatus. Nature 371, 62-64; doi:10.1038/371062a0
8. ^ Wang, X., Zhou Z., Zhang F. And Xu X., 2002. A nearly completely articulated rhamphorhynchoid pterosaur with exceptionally well-preserved wing membranes and "hairs" from Inner Mongolia, northeast China. Chinese Science Bulletin 47:3
9. ^ Dyke, G. J., Nudds, R. L. and Rayner, J. M. V., 2006. Limb disparity and wing shape in pterosaurs. Journal of Evolutionary Biology, 19:4 1339-1342(4); doi: 10.1111/j.1420-9101.2006.01096.x
10. ^ Webbed feet are also seen in some gliding animals such as colugos (the "flying lemurs")
11. ^ Padian, K. 2003. Pterosaur Stance and Gait and the Interpretation of Trackways, Ichnos 10:2-4 115-126 DOI: 10.1080/10420940390255501
12. ^ Hwang, K, Huh, M, Lockley M.G., Unwin D.M. and Wright, J.L. 2002. New pterosaur tracks (Pteraichnidae) from the Late Cretaceous Uhangri Formation, southwestern Korea Geological Magazine 139:4 421-435 DOI:10.1017/S0016756802006647
13. ^ Buffetaut, E., Martill, D., Escuillié, F. 2004. Pterosaurs as part of a spinosaur diet. Nature 430 33
14. ^ Ji, Q., Ji, S., Cheng, Y., You, H., Lü, J., Liu, Y., and Yuan, C. 2004. Pterosaur egg with a leathery shell. Nature 432, 572 doi:10.1038/432572a
15. ^ Wang, X., Zhou, Z., 2004. Pterosaur embryo from the Early Cretaceous. Nature 429, 621
16. ^ Grellet-Tinner, G., Wroe, S., Thompson, M.B., and Ji, Q. (2007). "A note on pterosaur nesting behavior." Historical Biology, 19(4): 273-277. doi: 10.1080/08912960701189800.
17. ^ Unwin, David M. (2006). The Pterosaurs: From Deep Time. New York: Pi Press, 246. ISBN ISBN 0-13-146308-X.
18. ^ Unwin, D. M., 2003: On the phylogeny and evolutionary history of pterosaurs. pp. 139-190. — in Buffetaut, E. & Mazin, J.-M., (eds.) (2003): Evolution and Palaeobiology of Pterosaurs. Geological Society of London, Special Publications 217, London, 1-347
19. ^ Slack, K. E., Jones, C. M., Ando, T., Harrison, G. L., Fordyce, R. E., Arnason, U. and Penny, D., 2006: Early Penguin Fossils, Plus Mitochondrial Genomes, Calibrate Avian Evolution. Molecular Biology and Evolution 23, 1144-1155; [2]
2. ^ Witmer W.M., Chatterjee, S., Franzosa, J. and Rowe, T. 2003. Neuroanatomy of flying reptiles and implications for flight, posture and behaviour. Nature 425, 950-953
3. ^ Bennett, S.C., 2000. Pterosaur flight: the role of actinofibrils in wing function. Historical Biology, 14:255-284.
4. ^ Wilkinson, M.T., Unwin, D.M. and Ellington, C.P., 2006. High lift function of the pteroid bone and forewing of pterosaurs, Proc Biol Sci. 273:1582 119-126 doi 10.1098/rspb.2005.3278
5. ^ Bennett, S.C., 2006 [Abstract] Articulation and function of the pteroid bone of pterosaurs. Journal of Vertebrate Paleontology, 26(Suppl. to #3):41A.
6. ^ Bennett, S.C. (2007). Reward for a Pteroid Errant. fhsu.edu/biology/cbennett/.
7. ^ Unwin, D.M. and Bakhurina, N.N., 1994. Sordes pilosus and the nature of the pterosaur flight apparatus. Nature 371, 62-64; doi:10.1038/371062a0
8. ^ Wang, X., Zhou Z., Zhang F. And Xu X., 2002. A nearly completely articulated rhamphorhynchoid pterosaur with exceptionally well-preserved wing membranes and "hairs" from Inner Mongolia, northeast China. Chinese Science Bulletin 47:3
9. ^ Dyke, G. J., Nudds, R. L. and Rayner, J. M. V., 2006. Limb disparity and wing shape in pterosaurs. Journal of Evolutionary Biology, 19:4 1339-1342(4); doi: 10.1111/j.1420-9101.2006.01096.x
10. ^ Webbed feet are also seen in some gliding animals such as colugos (the "flying lemurs")
11. ^ Padian, K. 2003. Pterosaur Stance and Gait and the Interpretation of Trackways, Ichnos 10:2-4 115-126 DOI: 10.1080/10420940390255501
12. ^ Hwang, K, Huh, M, Lockley M.G., Unwin D.M. and Wright, J.L. 2002. New pterosaur tracks (Pteraichnidae) from the Late Cretaceous Uhangri Formation, southwestern Korea Geological Magazine 139:4 421-435 DOI:10.1017/S0016756802006647
13. ^ Buffetaut, E., Martill, D., Escuillié, F. 2004. Pterosaurs as part of a spinosaur diet. Nature 430 33
14. ^ Ji, Q., Ji, S., Cheng, Y., You, H., Lü, J., Liu, Y., and Yuan, C. 2004. Pterosaur egg with a leathery shell. Nature 432, 572 doi:10.1038/432572a
15. ^ Wang, X., Zhou, Z., 2004. Pterosaur embryo from the Early Cretaceous. Nature 429, 621
16. ^ Grellet-Tinner, G., Wroe, S., Thompson, M.B., and Ji, Q. (2007). "A note on pterosaur nesting behavior." Historical Biology, 19(4): 273-277. doi: 10.1080/08912960701189800.
17. ^ Unwin, David M. (2006). The Pterosaurs: From Deep Time. New York: Pi Press, 246. ISBN ISBN 0-13-146308-X.
18. ^ Unwin, D. M., 2003: On the phylogeny and evolutionary history of pterosaurs. pp. 139-190. — in Buffetaut, E. & Mazin, J.-M., (eds.) (2003): Evolution and Palaeobiology of Pterosaurs. Geological Society of London, Special Publications 217, London, 1-347
19. ^ Slack, K. E., Jones, C. M., Ando, T., Harrison, G. L., Fordyce, R. E., Arnason, U. and Penny, D., 2006: Early Penguin Fossils, Plus Mitochondrial Genomes, Calibrate Avian Evolution. Molecular Biology and Evolution 23, 1144-1155; [2]
See also
External links
- Pterosaur FAQ's, by Raymond Thaddeus C. Ancog.
- The Pterosaur Database, by Paul Pursglove.
- The Pterosauria, by Mike Hanson.
- Comments on the phylogeny of the pterodactyloidea, by Alexander W. A. Kellner. (technical)
- Pterosaurs no bird brains
IMDb profile
All Movie Guide profile Pterodactyl is a 2005 film that premiered on the Sci Fi Channel. The film was directed by Mark L. Lester.
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All Movie Guide profile Pterodactyl is a 2005 film that premiered on the Sci Fi Channel. The film was directed by Mark L. Lester.
Plot
Professor Lovecraft (Cameron Daddo) is a paleontologist whose career is in a slump...... Click the link for more information.
The Westland-Hill Pterodactyl were a series of experimental aircraft designs starting in the 1920s named after the pterosaur.
They were designed by Geoffrey T. R. Hill and built by Westland Aircraft.
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They were designed by Geoffrey T. R. Hill and built by Westland Aircraft.
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The Triassic is a geologic period that extends from about 251 to 199 Ma (million years ago). As the first period of the Mesozoic Era, the Triassic follows the Permian and is followed by the Jurassic. Both the start and end of the Triassic are marked by major extinction events.
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The Cretaceous Period is one of the major divisions of the geologic timescale, reaching from the end of the Jurassic Period (i.e. from 145.5 ± 4.0 million years ago (Ma)) to the beginning of the Paleocene epoch of the Tertiary Period (about 65.5 ± 0.3 Ma).
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Coloborhynchus
Owen, 1874
Species
Coloborhynchus is a genus of the extinct Pterosauria, family Ornithocheiridae from the Lower Cretaceous of Europe, North America, and South America.
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Owen, 1874
Species
- see text
Coloborhynchus is a genus of the extinct Pterosauria, family Ornithocheiridae from the Lower Cretaceous of Europe, North America, and South America.
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Pterodactyloidea
Plieninger, 1901
Superfamilies
Azhdarchoidea
Ctenochasmatoidea
Dsungaripteroidea
Ornithocheiroidea
Pterodactyloidea (derived from the Greek words πτερόν (pterón
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Plieninger, 1901
Superfamilies
Azhdarchoidea
Ctenochasmatoidea
Dsungaripteroidea
Ornithocheiroidea
Pterodactyloidea (derived from the Greek words πτερόν (pterón
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Scientific classification or biological classification is a method by which biologists group and categorize species of organisms. Scientific classification also can be called scientific taxonomy, but should be distinguished from folk taxonomy, which lacks scientific basis.
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Chordata
Bateson, 1885
Typical Classes
See below
Chordates (phylum Chordata) are a group of animals that includes the vertebrates, together with several closely related invertebrates.
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Bateson, 1885
Typical Classes
See below
Chordates (phylum Chordata) are a group of animals that includes the vertebrates, together with several closely related invertebrates.
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Sauropsida*
Goodrich, 1916
Subclasses
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Goodrich, 1916
Subclasses
- Anapsida
- Diapsida
- Reptilia Laurenti, 1768
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Archosauria
Cope, 1869
Clades
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Cope, 1869
Clades
- Crurotarsi
- Aetosauria
- Crocodilia (crocodiles)
- Phytosauria
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Johann Jakob Kaup (April 10, 1803 - July 4, 1873) was a German naturalist.
He was born at Darmstadt. After studying at Göttingen and Heidelberg he spent two years at Leiden, where his attention was specially devoted to the amphibians and fishes.
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He was born at Darmstadt. After studying at Göttingen and Heidelberg he spent two years at Leiden, where his attention was specially devoted to the amphibians and fishes.
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Pterodactyloidea
Plieninger, 1901
Superfamilies
Azhdarchoidea
Ctenochasmatoidea
Dsungaripteroidea
Ornithocheiroidea
Pterodactyloidea (derived from the Greek words πτερόν (pterón
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Plieninger, 1901
Superfamilies
Azhdarchoidea
Ctenochasmatoidea
Dsungaripteroidea
Ornithocheiroidea
Pterodactyloidea (derived from the Greek words πτερόν (pterón
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Rhamphorhynchoidea*
Plieninger, 1901
Families
Anurognathidae
Campylognathoididae
Dimorphodontidae
Rhamphorhynchidae
The Rhamphorhynchoidea
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Plieninger, 1901
Families
Anurognathidae
Campylognathoididae
Dimorphodontidae
Rhamphorhynchidae
The Rhamphorhynchoidea
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In phylogenetics, a group of organisms is said to be paraphyletic (Greek para = near and phyle = race) if the group contains its most recent common ancestor, but does not contain all the descendants of that ancestor.
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Greek}}}
Writing system: Greek alphabet
Official status
Official language of: Greece
Cyprus
European Union
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Turkey
Regulated by:
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Writing system: Greek alphabet
Official status
Official language of: Greece
Cyprus
European Union
recognised as minority language in parts of:
European Union
Italy
Turkey
Regulated by:
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Sauropsida*
Goodrich, 1916
Subclasses
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Goodrich, 1916
Subclasses
- Anapsida
- Diapsida
- Reptilia Laurenti, 1768
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The Triassic is a geologic period that extends from about 251 to 199 Ma (million years ago). As the first period of the Mesozoic Era, the Triassic follows the Permian and is followed by the Jurassic. Both the start and end of the Triassic are marked by major extinction events.
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The Cretaceous Period is one of the major divisions of the geologic timescale, reaching from the end of the Jurassic Period (i.e. from 145.5 ± 4.0 million years ago (Ma)) to the beginning of the Paleocene epoch of the Tertiary Period (about 65.5 ± 0.3 Ma).
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A geologic period is a subdivision of geologic time that divides an era into smaller timeframes. The equivalent term used to demarcate rock layers and the fossil record is the system; thus the rocks of the Devonian System were laid down during the Devonian Period.
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Annum is a Latin noun meaning year. It is the accusative singular of the second declension masculine noun annus (nominative), anni (genitive) [1] .
As a unit of time, it is defined as exactly 365.
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As a unit of time, it is defined as exactly 365.
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Vertebrata
Cuvier, 1812
Classes and Clades
See below
Vertebrates are members of the subphylum Vertebrata (within the phylum Chordata), specifically, those chordates with backbones or spinal columns.
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Cuvier, 1812
Classes and Clades
See below
Vertebrates are members of the subphylum Vertebrata (within the phylum Chordata), specifically, those chordates with backbones or spinal columns.
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Biological tissue is a collection of interconnected cells that perform a similar function within an organism.
The study of tissue is known as histology, or, in connection with disease, histopathology.
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The study of tissue is known as histology, or, in connection with disease, histopathology.
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thorax is a division of an animal's body that lies between the head and the abdomen.
In mammals, the thorax is the region of the body formed by the sternum, the thoracic vertebrae and the ribs. It extends from the neck to the diaphragm, not including the upper limbs.
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In mammals, the thorax is the region of the body formed by the sternum, the thoracic vertebrae and the ribs. It extends from the neck to the diaphragm, not including the upper limbs.
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Dinosauria *
Owen, 1842
Orders & Suborders
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Owen, 1842
Orders & Suborders
- Ornithischia
- Cerapoda
- Thyreophora
- Saurischia
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Terrestrial animals are animals that live predominantly or entirely on land, as compared with aquatic animals, which live predominantly or entirely in the water (e.g., fish, lobsters, octopuses), or amphibians, which rely on a combination of aquatic and terrestrial habitats (e.g.
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Sauropsida*
Goodrich, 1916
Subclasses
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Goodrich, 1916
Subclasses
- Anapsida
- Diapsida
- Reptilia Laurenti, 1768
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Ichthyosauria
Blainville, 1835
Families
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Blainville, 1835
Families
- Ichthyosauridae
- Leptonectidae
- Mixosauridae
- Ophthalmosauridae
- Shastasauridae
- Stenopterygiidae
- Teretocnemidae
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Plesiosauroidea
Gray, 1825
Families
Cimoliasauridae
Cryptoclididae
Elasmosauridae
Plesiosauridae
Polycotylidae
Plesiosaurs (IPA /ˈplisɪəˌsɔɹ/
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Gray, 1825
Families
Cimoliasauridae
Cryptoclididae
Elasmosauridae
Plesiosauridae
Polycotylidae
Plesiosaurs (IPA /ˈplisɪəˌsɔɹ/
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Herod_Archelaus