Ophthalmosaurus (Greek ὀφθάλμος ophthalmos 'eye' and σαῦρος sauros 'lizard') is a genus of ichthyosaur known from the Middle-Late Jurassic. Possible remains from the earliest Cretaceous, around 145 million years ago, are also known. It was a relatively medium-sized ichthyosaur, measuring 4 m (13 ft) long and weighing 940 kg (2,070 lb).[2][3] Named for its extremely large eyes, it had a jaw containing many small but robust teeth. Major fossil finds of this genus have been recorded in Europe with a second species possibly being found in North America.
Ophthalmosaurus Temporal range: Middle Jurassic to Late Jurassic (Callovian to Oxfordian), Possible record during the Berriasian
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Composite skeleton (NHMUK PV R3702, R3893, R4124) of Ophthalmosaurus icenicus at the Natural History Museum, London, with the forelimbs mounted backwards[1] | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Order: | †Ichthyosauria |
Family: | †Ophthalmosauridae |
Subfamily: | †Ophthalmosaurinae |
Genus: | †Ophthalmosaurus Seeley 1874 |
Type species | |
†Ophthalmosaurus icenicus | |
Species | |
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Synonyms | |
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Description
editOphthalmosaurus was a medium-sized ichthyosaur, growing to measure 4 m (13 ft) in length and weighing between 930–950 kg (2,050–2,090 lb).[2][3] It had a robust, streamlined body that was nearly as wide as it was tall in frontal view. Like other derived ichthyosaurs Ophthalmosaurus had a powerful tail ending in a pronounced bi-lobed caudal fluke whose lower half was formed around the caudal spine whereas the upper lobe was made up entirely from soft tissue. The limbs of Ophthalmosaurus were short and rounded with the forelimbs being noticeably larger than the hind limbs. The combination of rather inflexible trunk, powerful caudal fluke and reduced limbs suggests a tail-propelled mode of locomotion with the limbs helping with steering, differing from the anguilliform (eel-like) way more basal ichthyosaurs swam. The skull of Ophthalmosaurus was long with a slender, toothed rostrum and an enlarged posterior portion of the cranium. The dentition was relatively small with robust tooth crowns and the lateral area of the cranium was almost entirely occupied by the animal's massive eyes that gave the genus its name. The proportionally large eyes of Ophthalmosaurus measured 22–23 centimetres (8.7–9.1 in) in diameter at the outer margin of the bony sclerotic ring, while the sclerotic aperture itself measured 10 centimetres (3.9 in) in diameter.[2][4]
Discovery and species
editOphthalmosaurus was first described by Harry Seeley in 1874 with particular focus on the morphology of the clavicular bones. Over the years following its description a variety of genera have been sunk into Ophthalmosaurus.[5] Among them, Apatodontosaurus, Ancanamunia, Baptanodon, Mollesaurus, Paraophthalmosaurus, Undorosaurus and Yasykovia were all considered junior synonyms of Ophthalmosaurus in a study published by Maisch & Matzke in 2000.[6]
However, more recent cladistic analyses have contested Maisch & Matzke's conclusion. Mollesaurus periallus from Argentina was considered a valid genus of ophthalmosaurid by Druckenmiller and Maxwell (2010),[7][8][9] Paraophthalmosaurus and Yasykovia were both recovered as distinct genera by Storrs et al., but were later sunk into Nannopterygius[10][11][12] while Undorosaurus's validity is now accepted by most authors, including Maisch (2010) who originally proposed the synonymy.[8][10][13][14][15] The two other Russian taxa might be also valid.[8][14] Likewise the Mexican ophthalmosaurid Jabalisaurus had also been referred to Ophthalmosaurus before being described as a distinct species and genus in 2021.[16]
Ophthalmosaurus natans was described as Sauranodon, then later renamed to Baptanodon by Marsh in 1880. However this decision was questioned not long afterwards with Baptanodon instead being considered an American species of Ophthalmosaurus. Recent analysis have recovered the species as closer to other ophthalmosaurines than to the Ophthalmosaurus type species,[7][9][17] suggesting that the previous name should be reinstated. Similarly, Ophthalmosaurus chrisorum, whose holotype has been recovered in Canada and described by Russell in 1993, was moved to its own genus Arthropterygius in 2010 by Maxwell.[18]
While primarily known from the Jurassic, material from the Spilsby Sandstone dating to the early Berriasian stage of the Lower Cretaceous has been referred to cf. Ophthalmosaurus (i.e., either Ophthalmosaurus or a closely related species).[19]
Classification
editWithin Ophthalmosauridae, Ophthalmosaurus was once considered most closely related to Aegirosaurus.[20] However, many recent cladistic analyses found Ophthalmosaurus to nest in a clade with Acamptonectes and Mollesaurus. Aegirosaurus was found more closely related to Platypterygius, and thus does not belong to the Ophthalmosaurinae.[8][9]
Phylogeny
editThe cladogram below follows Fischer et al. 2012.[9]
Thunnosauria |
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The following cladogram shows a possible phylogenetic position of Ophthalmosaurus in Ophthalmosauridae according to the analysis performed by Zverkov and Jacobs (2020).[12]
Ophthalmosauria |
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Palaeobiology
editOphthalmosaurus icenicus possessed small teeth with robust tooth crowns and signs of slight wear differing notably from the robust teeth of later species of Platypterygius, known to have hunted large prey including turtles and birds, and the minute teeth of Baptanodon, interpreted to be a soft prey specialist. Fischer et al. (2016) conclude that this intermediary tooth morphology indicates that Ophthalmosaurus icenicus was most likely a generalist predator, feeding on a variety of smaller prey items.[22]
Ophthalmosaurus could likely dive for around 20 minutes. Assuming a conservative cruising speed of 1 metre per second (3.3 ft/s) (2 metres per second (6.6 ft/s) being more likely), Ophthalmosaurus could reach depths of 600 metres (2,000 ft) or more during a dive, reaching the mesopelagic zone.[3] However, while studies on the biomechanics of Ophthalmosaurus suggests that such feats could be physically achieved, studies on the environment of the Peterborough member of the Oxford Clay suggest that Ophthalmosaurus instead inhabited relatively shallow waters there, being determined to have been just 50 metres (160 ft) deep at a distance of 150 kilometres (93 mi) from the shore.[23]
See also
editReferences
edit- ^ Moon, B. C.; Kirton, A. M. (2016). "Ichthyosaurs of the British Middle and Upper Jurassic. Part 1, Ophthalmosaurus". Monographs of the Palaeontographical Society. 170 (647): 1–84. Bibcode:2016MPalS.170....1M. doi:10.1080/02693445.2016.11963958. hdl:1983/983f82bf-a391-4cbc-b313-1fc754017eef. S2CID 133288616.
- ^ a b c Motani, Ryosuke; Rothschild, Bruce M.; Wahl, William (1999). "Large eyeballs in diving ichthyosaurs" (PDF). Nature. 402 (6763): 747. Bibcode:1999Natur.402..747M. doi:10.1038/45435. ISSN 1476-4687. S2CID 5432366. Archived from the original (PDF) on 18 January 2017.
- ^ a b c Motani, Ryosuke (2005). "Evolution of fish-shaped reptiles (Reptilia: Ichthyopterygia) in their physical environments and constraints" (PDF). Annual Review of Earth and Planetary Sciences. 33: 395–420. Bibcode:2005AREPS..33..395M. doi:10.1146/annurev.earth.33.092203.122707. S2CID 54742104. Archived from the original (PDF) on 2019-07-07.
- ^ Schwab, Ivan R (2002). "My, what big eyes you have . . ". The British Journal of Ophthalmology. 86 (2): 130. doi:10.1136/bjo.86.2.130. ISSN 0007-1161. PMC 1771016. PMID 11855367.
- ^ H.G. Seeley (1874). "On the Pectoral Arch and Fore Limbs of Ophthalmosaurus, a new Ichthyosaurian Genus from the Oxford Clay". Quarterly Journal of the Geological Society. 30 (1–4): 696–707. doi:10.1144/gsl.jgs.1874.030.01-04.64. S2CID 129725722.
- ^ Maisch MW, Matzke AT. 2000. The Ichthyosauria. Stuttgarter Beiträge zur Naturkunde, Serie B (Geologie und Paläontologie) 298: 1-159.
- ^ a b Patrick S. Druckenmiller; Erin E. Maxwell (2010). "A new Lower Cretaceous (lower Albian) ichthyosaur genus from the Clearwater Formation, Alberta, Canada". Canadian Journal of Earth Sciences. 47 (8): 1037–1053. Bibcode:2010CaJES..47.1037D. doi:10.1139/E10-028.[permanent dead link ]
- ^ a b c d Fischer, Valentin; Edwige Masure; Maxim S. Arkhangelsky; Pascal Godefroit (2011). "A new Barremian (Early Cretaceous) ichthyosaur from western Russia". Journal of Vertebrate Paleontology. 31 (5): 1010–1025. Bibcode:2011JVPal..31.1010F. doi:10.1080/02724634.2011.595464. hdl:2268/92828. S2CID 86036325.
- ^ a b c d Valentin Fischer; Michael W. Maisch; Darren Naish; Ralf Kosma; Jeff Liston; Ulrich Joger; Fritz J. Krüger; Judith Pardo Pérez; Jessica Tainsh; Robert M. Appleby (2012). "New Ophthalmosaurid Ichthyosaurs from the European Lower Cretaceous Demonstrate Extensive Ichthyosaur Survival across the Jurassic–Cretaceous Boundary". PLOS ONE. 7 (1): e29234. Bibcode:2012PLoSO...729234F. doi:10.1371/journal.pone.0029234. PMC 3250416. PMID 22235274.
- ^ a b Storrs, Glenn W.; Vladimir M. Efimov; Maxim S. Arkhangelsky (2000). "Mesozoic marine reptiles of Russia and other former Soviet republics". In Benton, M.J.; Shishkin, M.A.; Unwin, D.M. (eds.). The Age of Dinosaurs in Russia and Mongolia. Cambridge: Cambridge University Press. pp. 140–210. ISBN 9780521545822.
- ^ N. G. Zverkov, M. S. Arkhangelsky and I. M. Stenshin (2015) A review of Russian Upper Jurassic ichthyosaurs with an intermedium/humeral contact. Reassessing Grendelius McGowan, 1976. Proceedings of the Zoological Institute 318(4): 558-588
- ^ a b Nikolay G. Zverkov & Megan L. Jacobs (2021) [First published 2020]. "Revision of Nannopterygius (Ichthyosauria: Ophthalmosauridae): reappraisal of the 'inaccessible' holotype resolves a taxonomic tangle and reveals an obscure ophthalmosaurid lineage with a wide distribution". Zoological Journal of the Linnean Society. 191 (1): 228–275. doi:10.1093/zoolinnean/zlaa028.
- ^ McGowan C, Motani R. 2003. Ichthyopterygia. – In: Sues, H.-D. (ed.): Handbook of Paleoherpetology, Part 8, Verlag Dr. Friedrich Pfeil, 175 pp., 101 figs., 19 plts; München
- ^ a b Michael W. Maisch (2010). "Phylogeny, systematics, and origin of the Ichthyosauria – the state of the art" (PDF). Palaeodiversity. 3: 151–214.
- ^ Fischer, V.; A. Clement; M. Guiomar; P. Godefroit (2011). "The first definite record of a Valanginian ichthyosaur and its implications on the evolution of post-Liassic Ichthyosauria". Cretaceous Research. 32 (2): 155–163. Bibcode:2011CrRes..32..155F. doi:10.1016/j.cretres.2010.11.005. hdl:2268/79923. S2CID 45794618.
- ^ Barrientos-Lara, Jair Israel; Alvarado-Ortega, Jesús (2021-11-01). "A new ophthalmosaurid (Ichthyosauria) from the Upper Kimmeridgian deposits of the La Casita Formation, near Gómez Farías, Coahuila, northern Mexico". Journal of South American Earth Sciences. 111: 103499. Bibcode:2021JSAES.11103499B. doi:10.1016/j.jsames.2021.103499. ISSN 0895-9811.
- ^ Paparella, Ilaria; Maxwell, Erin E.; Cipriani, Angelo; Roncacè, Scilla; Caldwell, Michael W. (2017). "The first ophthalmosaurid ichthyosaur from the Upper Jurassic of the Umbrian-Marchean Apennines (Marche, Central Italy)". Geological Magazine. 154 (4): 837. Bibcode:2017GeoM..154..837P. doi:10.1017/S0016756816000455. S2CID 132955874.
- ^ Maxwell, E.E. (2010). "Generic reassignment of an ichthyosaur from the Queen Elizabeth Islands, Northwest Territories, Canada". Journal of Vertebrate Paleontology. 30 (2): 403–415. Bibcode:2010JVPal..30..403M. doi:10.1080/02724631003617944. S2CID 85143039.
- ^ Fischer, V.; Maisch, M. W.; Naish, D.; Kosma, R.; Liston, J.; Joger, U.; Krüger, F. J.; Pérez, J. P.; Tainsh, J.; Appleby, R. M.; Fenton, B. (2012). "New ophthalmosaurid ichthyosaurs from the European Lower Cretaceous demonstrate extensive ichthyosaur survival across the Jurassic–Cretaceous boundary". PLOS ONE. 7 (1): e29234. Bibcode:2012PLoSO...729234F. doi:10.1371/journal.pone.0029234. PMC 3250416. PMID 22235274.
- ^ Fernández M. 2007. Redescription and phylogenetic position of Caypullisaurus (Ichthyosauria: Ophthalmosauridae). Journal of Paleontology 81 (2): 368-375.
- ^ Arkhangel’sky, M. S., 1998, On the Ichthyosaurian Genus Platypterygius: Palaeontological Journal, v. 32, n. 6, p. 611-615.
- ^ Fischer, V.; Bardet, N.; Benson, R.B.J.; Arkhangelsky, M.S.; Friedman, M. (2016). "Extinction of Fish-shaped Marine Reptiles Associated with Reduced Evolutionary Rates and Global Environmental Volatility". Nature Communications. 7: 10825. Bibcode:2016NatCo...710825F. doi:10.1038/ncomms10825. PMC 4786747. PMID 26953824.
- ^ Hudson, John D.; Martill, David M. (1991). "The Lower Oxford Clay: production and preservation of organic matter in the Callovian (Jurassic) of central England". Geological Society, London, Special Publications. 58 (1): 363–379. Bibcode:1991GSLSP..58..363H. doi:10.1144/GSL.SP.1991.058.01.23. S2CID 129388168.