Dimorphodon

Summary

Dimorphodon /dˈmɔːrfədɒn/ was a genus of medium-sized pterosaur from Europe during the early Jurassic Period (about 201-191 million years ago).[1] It was named by paleontologist Richard Owen in 1859. Dimorphodon means "two-form tooth", derived from the Greek δι (di) meaning "two", μορφη (morphe) meaning "shape" and οδων (odon) meaning "tooth", referring to the fact that it had two distinct types of teeth in its jaws – which is comparatively rare among reptiles. The diet of Dimorphodon has been questioned among researchers, with earlier interpretations depicting it as an insectivore or a piscivore. Recent studies have suggested that Dimorphodon likely hunted small vertebrates, though it still would have consumed soft invertebrates like insects.

Dimorphodon
Temporal range: Early Jurassic (Sinemurian), 201.3–189.6 Ma
Reconstruction skeleton in flying pose at the Rocky Mountain Dinosaur Resource Center
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Order: Pterosauria
Clade: Macronychoptera
Family: Dimorphodontidae
Subfamily: Dimorphodontinae
Seeley, 1870
Genus: Dimorphodon
Owen, 1859
Type species
Dimorphodon macronyx
(Buckland, 1829)
Species
  • D. macronyx (Buckland, 1829)
Synonyms
  • Pterodactylus macronyx Buckland, 1829
  • Pterodactylus (Rhamphorhynchus) macronyx (Buckland, 1829)

Description edit

 
Restoration of a pair of D. macronyx

The body structure of Dimorphodon displays many "primitive" characteristics, such as, according to Owen, a very small brain-pan[2] and proportionally short wings.[2] The first phalanx in its flight finger is only slightly longer than its lower arm.[2] The neck was short but strong and flexible and may have had a membranous pouch on the underside. The vertebrae had pneumatic foramina, openings through which the air sacs could reach the hollow interior. Dimorphodon had an adult body length of 1 metre (3.3 ft) long, with a 1.45 metre (4.6 ft) wingspan.[2][3] The tail of Dimorphodon was long and consisted of thirty vertebrae. The first five or six were short and flexible, but the remainder gradually increased in length and were stiffened by elongated vertebral processes.[2] The terminal end of the tail may have borne a Rhamphorhynchus-like tail vane, although no impressions have yet been found in Dimorphodon fossils to confirm this speculation.[2]

Skull edit

Dimorphodon had a large, bulky skull approximately 23 centimetres (9.1 in) in length, whose weight was reduced by large openings separated from each other by thin bony partitions.[2] Its structure, reminiscent of the supporting arches of a bridge, prompted Richard Owen to declare that, as far as achieving great strength from lightweight materials was concerned, no vertebra was more economically constructed; Owen saw the vertebrate skull as a combination of four vertebrae modified from the ideal type of the vertebra.[4] The front of the upper jaw had four or five fang-like teeth followed by an indeterminate number of smaller teeth; the maxilla of all exemplars is damaged at the back. The lower jaw had five longer teeth and thirty to forty tiny, flattened pointed teeth, shaped like lancets.[2] Many depictions give it a speculative puffin-like 'beak' because of similarities between the two animals' skulls.

History of discovery edit

 
D. macronyx holotype specimen, NHMUK PV R 1034

The first fossil remains now attributed to Dimorphodon were found in England by fossil collector Mary Anning, at Lyme Regis in Dorset, UK in December 1828.[5] This region of Britain is now a World Heritage Site, dubbed the Jurassic Coast; in it layers of the Blue Lias are exposed, dating from the Hettangian-Sinemurian. The specimen was acquired by William Buckland and reported in a meeting of the Geological Society on 5 February 1829.[6] In 1835, after a thorough study by William Clift and William John Broderip, this report, strongly expanded, was published in the Transactions of the Geological Society, describing and naming the fossil as a new species. As was the case with most early pterosaur finds, Buckland classified the remains in the genus Pterodactylus, coining the new species Pterodactylus macronyx.[7] The specific name is derived from Greek makros, "large" and onyx, "claw", in reference to the large claws of the hand. The specimen, presently NHMUK PV R 1034, consisted of a partial and disarticulated skeleton on a slab, lacking the skull. Buckland in 1835 also assigned a piece of jaw from the collection of Elizabeth Philpot to P. macronyx. Later, the many putative species assigned to Pterodactylus had become so anatomically diverse that they began to be broken into separate genera.

 
Illustration of D. macronyx specimen NHUK PV R 1035

In 1858, Richard Owen reported finding two new specimens, NHMUK PV OR 41212 and NHMUK PV R 1035, again partial skeletons but this time including the skulls. Having found the skull to be very different from that of Pterodactylus, Owen assigned Pterodactylus macronyx its own genus, which he named Dimorphodon.[8] His first report contained no description and the name remained a nomen nudum. In 1859, however, a subsequent publication by Owen provided a description.[9] After several studies highlighting aspects of Dimorphodon's anatomy, Owen in 1874 made NHMUK PV R 1034 the holotype.[10]

 
Cast of D. macronyx specimen NHMUK PV OR 41212

Meanwhile, though Dimorphodon is not a very common fossil, other fragmentary specimens were found. Some of these were acquired by Othniel Charles Marsh between 1873 and 1881 from the London fossil dealer Bryce McMurdo Wright. One of these had been recovered from early Jurassic strata at the south bank of the Severn river, at the Aust Cliff.[2]

An additional species of Dimorphodon, D. weintraubi, was named by James Clark et al in 1998 from a partial skeleton recovered in siltstones from the site Huizachal Canyon in La Boca Formation in Tamaulipas, Mexico, from the Early Jurassic (Pliensbachian), where remains of sphenodontians, dinosaurs and mammaliaforms have also been found.[11] It is known from the type specimen, IGM 3494 (Instituto Geológico de México, of the Universidad Nacional Autónoma de México), that comprises articulated pieces of the skeleton including the posterior part of skull, four cervical vertebrae, the scapulocoracoids, left humerus, partial right wing and right leg distal to mid tibiotarsus. This specimen is larger than D. macronyx and the well preserved foot of it shows that pterosaurs do not have a digitigrade posture in their hindlimbs, but that it have a plantigrade gait, as has been inferred from footprints. The name of the species is a homage to Dr. Robert L. Weintraub.[12] Later studies considered this species not closely related to Dimorphodon macronyx, but an early relative of Anurognathidae.[13]

Classification edit

 
Reconstructed skeleton, Rainbow Forest Museum

In 1870, Seeley assigned Dimorphodon to its own family, Dimorphodontidae, with Dimorphodon as the only member. It was suggested in 1991 by the German paleontologist Peter Wellnhofer that Dimorphodon might be descended from the earlier European pterosaur Peteinosaurus.[2] Later exact cladistic analyses are not in agreement. According to Unwin, Dimorphodon was related to, though probably not a descendant of, Peteinosaurus, both forming the clade Dimorphodontidae, the most basal group of the Macronychoptera and within it the sister group of the Caelidracones. This would mean that both dimorphodontid species would be the most basal pterosaurs known with the exception of Preondactylus. According to Alexander Kellner, however, Dimorphodon is far less basal and not a close relative of Peteinosaurus.

The cladogram recovered by Andres and Myers in 2013 is reproduced below.[14]

Pterosauria

Palaeobiology edit

Diet edit

 
Restoration of D. macronyx chasing a sphenodontian on the ground

The knowledge of how Dimorphodon lived is limited. It perhaps mainly inhabited coastal regions and might have had a very varied diet. Buckland suggested it ate insects. Later, it became common to depict it as a piscivore (fish eater), though biomechanical studies support Buckland's original insectivore idea better, and inconsistent with the animal's habits (see flight below). Dimorphodon had an advanced jaw musculature specialized for a "snap and hold" method of feeding. The jaw could close extremely quickly, but with relatively little force or tooth penetration. This, along with the short and high skull and longer, pointed front teeth suggest that Dimorphodon was an insectivore, though it may have occasionally eaten small vertebrates and carrion as well.[15] Mark Witton has argued that the animal was a specialised carnivore that was too large for an insectivorous diet, though he did acknowledge that it still might have ate large insects, and thus specialised to hunt relatively small vertebrates, with its relatively weak jaw musculature indicating that it probably ate proportionally small prey.[16] Dental microwear examinations confirm its status as a vertebrate predator, as opposed to several other insectivore or piscivore early pterosaurs, though the study does acknowledge that the possibility of consuming relatively softer invertebrates cannot be excluded entirely.[17]

Locomotion edit

Like many pterosaurs, Dimorphodon has been perceived as a soarer in the past, correlating to historical perceptions of pterosaurs as seabird analogues. However, more recent studies show that the animal was actually a rather poor flyer: its wings are proportionally short in relation to the body and its skeleton rather robust, offering very little gliding potential. In life, Dimorphodon probably relied on frantic short flights in the same manner as modern fowl, tinamous and woodpeckers, being unable to fly for long distances and probably only taking to the air as a last resort.[16][18]

 
Restoration of D. macronyx in flight

Its derived position amidst primitive pterosaurs implies that this ineptitude is a developed trait, not an ancestral characteristic, as earlier pterosaurs like Preondactylus were capable aeronauts.

 
D. macronyx in the controversial bipedal pose, Seeley, 1901
 
Seeley's quadrupedal Dimorphodon pose

Owen saw Dimorphodon as a quadruped. He speculated that the fifth toe supported a membrane between the tail and the legs and that the animal was therefore very ungainly on the ground.[2] However, his rival Harry Govier Seeley, propagating the view that pterosaurs were warm-blooded and active, argued that Dimorphodon was either an agile quadruped or even a running biped due to its relatively well developed hindlimbs and characteristics of its pelvis.[19] This hypothesis was revived by Kevin Padian in 1983.[20] However, fossilised track remains of other pterosaurs (ichnites) show a quadrupedal gait while on the ground and these traces are all attributed to derived pterosaurs with a short fifth toe. Dimorphodon's was elongated, clawless, and oriented to the side.[2] David Unwin has therefore argued that even Dimorphodon was a quadruped, a view confirmed by computer modelling by Sarah Sangster.[21]

Like most non-pterodactyloid pterosaurs, Dimorphodon was a competent climber, possessing proportionally large and curved ungals and a low center of gravity. Like modern squirrels, it probably moved in a saltatorial manner as it climbed.[16]

See also edit

References edit

  1. ^ Müller R.T., Ezcurra M.D., Garcia M.S., Agnolín F.L., Stocker M.R., Novas F.E., Soares M.B., Kellner A.W.A. & Nesbitt S.J. (2023). ”New reptile shows dinosaurs and pterosaurs evolved among diverse precursors”. Nature 620(7974): p. 589–594. doi:10.1038/s41586-023-06359-z
  2. ^ a b c d e f g h i j k l "Dimorphodon." In: Cranfield, Ingrid (ed.). The Illustrated Directory of Dinosaurs and Other Prehistoric Creatures. London: Salamander Books, Ltd. Pp. 288-291.
  3. ^ Wellnhofer, Peter (1996) [1991]. The Illustrated Encyclopedia of Pterosaurs. New York: Barnes and Noble Books. p. 71. ISBN 0-7607-0154-7.
  4. ^ Padian. K. (1995). "Pterosaurs and Typology: Archetypal Physiology in the Owen-Seeley Dispute of 1870", In: Sarjeant, W.A.S. & Halstead, L.N. (ed.) Vertebrate fossils and the evolution of scientific concepts: writings in tribute to Beverly Halstead, by some of his many friends, Gordon & Breach 1995
  5. ^ Wellnhofer, Peter (1996) [1991]. The Illustrated Encyclopedia of Pterosaurs. New York: Barnes and Noble Books. p. 69. ISBN 0-7607-0154-7.
  6. ^ Buckland, W. (1829). Proceedings of the Geological Society of London, 1: 127
  7. ^ Buckland, W. (1 January 1829). "XI.--On the Discovery of a New Species of Pterodactyle in the Lias at Lyme Regis". Transactions of the Geological Society of London. s2-3 (1): 217–222. doi:10.1144/transgslb.3.1.217. S2CID 129251962.
  8. ^ Owen, R. (1859). "On a new genus (Dimorphodon) of pterodactyle, with remarks on the geological distribution of flying reptiles". Report for the British Association for the Advancement of Science. 28: 97–103.
  9. ^ "II. On the vertebral characters of the order pterosauria (ow.) as exemplified in the genera Pterodactylus (cuv.) and Dimorphodon (ow.)". Proceedings of the Royal Society of London. 9: 703–704. 31 December 1859. doi:10.1098/rspl.1857.0143. S2CID 186208842.
  10. ^ Owen, R. (1874). "Monograph of the fossil Reptilia of the Mesozoic Formations. Part I. Pterosauria". Palaeontographical Society of London. 27: 1–14.
  11. ^ Montellano, Marisol; Hopson, James A.; Clark, James M. (2008). "Late Early Jurassic Mammaliaforms from Huizachal Canyon, Tamaulipas, México". Journal of Vertebrate Paleontology. 28 (4): 1130–1143. Bibcode:2008JVPal..28.1130M. doi:10.1671/0272-4634-28.4.1130. JSTOR 20491044. S2CID 128782275.
  12. ^ Clark, J. M.; Hopson, J. A.; Hernández R., R.; Fastovsky, D. E.; Montellano, M. (February 1998). "Foot posture in a primitive pterosaur" (PDF). Nature. 391 (6670): 886–889. Bibcode:1998Natur.391..886C. doi:10.1038/36092. S2CID 4408637.
  13. ^ Wei, Xuefang; Pêgas, Rodrigo Vargas; Shen, Caizhi; Guo, Yanfang; Ma, Waisum; Sun, Deyu; Zhou, Xuanyu (2021-03-31). "Sinomacrops bondei, a new anurognathid pterosaur from the Jurassic of China and comments on the group". PeerJ. 9: e11161. doi:10.7717/peerj.11161. ISSN 2167-8359. PMC 8019321. PMID 33850665.
  14. ^ Andres, Brian; Myers, Timothy S. (September 2012). "Lone Star Pterosaurs". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 103 (3–4): 383–398. doi:10.1017/S1755691013000303. S2CID 84617119.
  15. ^ Ősi, Attila (June 2011). "Feeding-related characters in basal pterosaurs: implications for jaw mechanism, dental function and diet: Feeding-related characters in pterosaurs" (PDF). Lethaia. 44 (2): 136–152. doi:10.1111/j.1502-3931.2010.00230.x.
  16. ^ a b c Wilton, Mark P. (2013). Pterosaurs: Natural History, Evolution, Anatomy. Princeton University Press. p. 103. ISBN 978-0-691-15061-1.
  17. ^ Bestwick, Jordan; Unwin, David M.; Butler, Richard J.; Purnell, Mark A. (28 October 2020). "Dietary diversity and evolution of the earliest flying vertebrates revealed by dental microwear texture analysis". Nature Communications. 11 (1): 5293. Bibcode:2020NatCo..11.5293B. doi:10.1038/s41467-020-19022-2. PMC 7595196. PMID 33116130.
  18. ^ Rayner et al 2011[full citation needed]
  19. ^ Seeley, Harry G. (August 1870). "X.— Remarks on Prof. Owen's monograph on Dimorphodon". Annals and Magazine of Natural History. 6 (32): 129–152. doi:10.1080/00222937008696217.
  20. ^ Padian, Kevin (1983). "Osteology and functional morphology of Dimorphodon macronyx (Buckland) (Pterosauria: Rhamphorhynchoidea) based on new material in the Yale Peabody Museum" (PDF). Postilla. 189: 1–44. Archived from the original (PDF) on 2021-01-26. Retrieved 2019-02-08.
  21. ^ Sangster, S. (2001). "Anatomy, functional morphology and systematics of Dimorphodon". Strata. 11: 87–88.