Ichthyosauria
Extinct order of large marine reptiles / From Wikipedia, the free encyclopedia
Dear Wikiwand AI, let's keep it short by simply answering these key questions:
Can you list the top facts and stats about Ichthyosaur?
Summarize this article for a 10 year old
Ichthyosauria (Ancient Greek for "fish lizard" – Ancient Greek: ἰχθύς, romanized: ichthys, lit. 'fish' and Ancient Greek: σαῦρος, romanized: sauros, lit. 'lizard') is an order of large extinct marine reptiles sometimes referred to as "ichthyosaurs", although the term is also used for wider clades that the order resides in.
Ichthyosauria | |
---|---|
Skeleton of Ichthyosaurus somersetensis | |
Life restoration of Ophthalmosaurus | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Clade: | †Eoichthyosauria |
Order: | †Ichthyosauria Blainville, 1835 |
Subgroups | |
See text |
Ichthyosaurians thrived during much of the Mesozoic era; based on fossil evidence, they first appeared around 250 million years ago (Ma) and at least one species survived until about 90 million years ago,[1][2] into the Late Cretaceous. During the Early Triassic epoch, ichthyosaurs and other ichthyosauromorphs evolved from a group of unidentified land reptiles that returned to the sea, in a development similar to how the mammalian land-dwelling ancestors of modern-day dolphins and whales returned to the sea millions of years later, which they gradually came to resemble in a case of convergent evolution. Ichthyosaurians were particularly abundant in the Late Triassic and Early Jurassic periods, until they were replaced as the top aquatic predators by another marine reptilian group, the Plesiosauria, in the later Jurassic and Early Cretaceous, though previous views of ichthyosaur decline during this period are probably overstated. Ichthyosaurians diversity declined due to environmental volatility caused by climatic upheavals in the early Late Cretaceous, becoming extinct around the Cenomanian-Turonian boundary approximately 90 million years ago.
Scientists became aware of the existence of ichthyosaurians during the early 19th century, when the first complete skeletons were found in England. In 1834, the order Ichthyosauria was named. Later that century, many excellently preserved ichthyosaurian fossils were discovered in Germany, including soft-tissue remains. Since the late 20th century, there has been a revived interest in the group, leading to an increased number of named ichthyosaurs from all continents, with over fifty valid genera being now known.
Ichthyosaurian species varied from 1 to 20 metres (3 to 66 ft) in length. Ichthyosaurians resembled both modern fish and dolphins. Their limbs had been fully transformed into flippers, which sometimes contained a very large number of digits and phalanges. At least some species possessed a dorsal fin. Their heads were pointed, and the jaws often were equipped with conical teeth to catch smaller prey. Some species had larger, bladed teeth to attack large animals. The eyes were very large, for deep diving. The neck was short, and later species had a rather stiff trunk. These also had a more vertical tail fin, used for a powerful propulsive stroke. The vertebral column, made of simplified disc-like vertebrae, continued into the lower lobe of the tail fin. Ichthyosaurians were air-breathing, warm-blooded, and bore live young. They may have had a layer of blubber for insulation.
Early finds
The first known illustrations of ichthyosaur bones, vertebrae, and limb elements were published by the Welshman Edward Lhuyd in his Lithophylacii Brittannici Ichnographia of 1699. Lhuyd thought that they represented fish remains.[3] In 1708, the Swiss naturalist Johann Jakob Scheuchzer described two ichthyosaur vertebrae assuming they belonged to a man drowned in the Universal Deluge.[4] In 1766, an ichthyosaur jaw with teeth was found at Weston near Bath. In 1783, this piece was exhibited by the Society for Promoting Natural History as those of a crocodilian. In 1779, ichthyosaur bones were illustrated in John Walcott's Descriptions and Figures of Petrifications.[5] Towards the end of the eighteenth century, British fossil collections quickly increased in size. Those of the naturalists Ashton Lever and John Hunter were acquired in their totality by museums; later, it was established that they contained dozens of ichthyosaur bones and teeth. The bones had typically been labelled as belonging to fish, dolphins, or crocodiles; the teeth had been seen as those of sea lions.[6]
The demand by collectors led to more intense commercial digging activities. In the early nineteenth century, this resulted in the discovery of more complete skeletons. In 1804, Edward Donovan at St Donats uncovered a four-metre-long (13 ft) ichthyosaur specimen containing a jaw, vertebrae, ribs, and a shoulder girdle. It was considered to be a giant lizard. In October 1805, a newspaper article reported the find of two additional skeletons, one discovered at Weston by Jacob Wilkinson, the other, at the same village, by Reverend Peter Hawker. In 1807, the last specimen was described by the latter's cousin, Joseph Hawker.[7] This specimen thus gained some fame among geologists as 'Hawker's Crocodile'. In 1810, near Stratford-upon-Avon, an ichthyosaur jaw was found that was combined with plesiosaur bones to obtain a more complete specimen, indicating that the distinctive nature of ichthyosaurs was not yet understood, awaiting the discovery of far better fossils.
The first complete skeletons
In 1811, in Lyme Regis, along what is now called the Jurassic Coast of Dorset, the first complete ichthyosaur skull was found by Joseph Anning, the brother of Mary Anning, who in 1812 while still a young girl, secured the torso of the same specimen. Their mother, Molly Anning, sold the combined piece to squire Henry Henley for £23. Henley lent the fossil to the London Museum of Natural History of William Bullock. When this museum was closed, the British Museum bought the fossil for a price of £47/5s;[verification needed] it still belongs to the collection of the now independent Natural History Museum and has the inventory number BMNH R.1158. It has been identified as a specimen of Temnodontosaurus platyodon.
In 1814, the Annings' specimen was described by Professor Everard Home, in the first scientific publication dedicated to an ichthyosaur.[8] Intrigued by the strange animal, Home tried to locate additional specimens in existing collections. In 1816, he described ichthyosaur fossils owned by William Buckland and James Johnson.[9] In 1818, Home published data obtained by corresponding with naturalists all over Britain.[10] In 1819, he wrote two articles about specimens found by Henry Thomas De la Beche and Thomas James Birch. A last publication of 1820 was dedicated to a discovery by Birch at Lyme Regis.[11] The series of articles by Home covered the entire anatomy of ichthyosaurs, but highlighted details only; a systematic description was still lacking.
Home felt very uncertain how the animal should be classified. Though most individual skeletal elements looked very reptilian, the anatomy as a whole resembled that of a fish, so he initially assigned the creature to the fishes, as seemed to be confirmed by the flat shape of the vertebrae. At the same time, he considered it a transitional form between fishes and crocodiles, not in an evolutionary sense, but as regarded its place in the scala naturae, the "Chain of Being" hierarchically connecting all living creatures. In 1818, Home noted some coincidental similarities between the coracoid of ichthyosaurians and the sternum of the platypus. This induced him to emphasize its status as a transitional form, combining, like the platypus, traits of several larger groups. In 1819, he considered it a form between newts, like the olm, and lizards; he now gave a formal generic name: Proteo-Saurus.[12][13] However, in 1817, Karl Dietrich Eberhard Koenig had already referred to the animal as Ichthyosaurus, "fish saurian" from Greek ἰχθύς, ichthys, "fish". This name at the time was an invalid nomen nudum and was only published by Koenig in 1825,[14] but was adopted by De la Beche in 1819 in a lecture where he named three Ichthyosaurus species. This text would only be published in 1822, just after De la Beche's friend William Conybeare published a description of these species, together with a fourth one.[15] The type species was Ichthyosaurus communis, based on a now lost skeleton. Conybeare considered that Ichthyosaurus had priority relative to Proteosaurus. Although this is incorrect by present standards, the latter name became a "forgotten" nomen oblitum. In 1821, De la Beche and Conybeare provided the first systematic description of ichthyosaurs, comparing them to another newly identified marine reptile group, the Plesiosauria.[16] Much of this description reflected the insights of their friend, the anatomist Joseph Pentland.
In 1835, the order Ichthyosauria was named by Henri Marie Ducrotay de Blainville.[17] In 1840, Richard Owen named an order Ichthyopterygia as an alternative concept.[18]
Popularisation during the 19th century
The discovery of a hitherto unsuspected extinct group of large marine reptiles generated much publicity, capturing the imagination of both scientists and the public at large. People were fascinated by the strange build of the animals, especially the large scleral rings in the eye sockets,[19] of which it was sometimes erroneously assumed these would have been visible on the living animal. Their bizarre form induced a feeling of alienation, allowing people to realise the immense span of time passed since the era in which the ichthyosaur swam the oceans.[20] Not all were convinced that ichthyosaurs had gone extinct: Reverend George Young found a skeleton in 1819 at Whitby; in his 1821 description, he expressed the hope that living specimens could still be found.[21] Geologist Charles Lyell, to the contrary, assumed that the Earth was eternal so that in the course of time the ichthyosaur might likely reappear, a possibility lampooned in a famous caricature by De la Beche.
Public awareness was increased by the works of the eccentric collector Thomas Hawkins, a pre-Adamite believing that ichthyosaurs were monstrous creations by the devil: Memoirs of Ichthyosauri and Plesiosauri of 1834[22] and The Book of the Great Sea-Dragons of 1840.[23] The first work was illustrated by mezzotints by John Samuelson Templeton. These publications also contained scientific descriptions and represented the first textbooks of the subject. In the summer of 1834, Hawkins, after a taxation by William Buckland and Gideon Mantell, sold his extensive collection, then the largest of its kind in the world, to the British Museum. However, curator Koenig quickly discovered that the fossils had been heavily restored with plaster, applied by an Italian artist from Lucca; of the most attractive piece, an Ichthyosaurus specimen, almost the entire tail was fake. It turned out that Professor Buckland had been aware of this beforehand, and the museum was forced to reach a settlement with Hawkins, and gave the fake parts a lighter colour to differentiate them from the authentic skeletal elements.[24]
Ichthyosaurs became even more popular in 1854 by the rebuilding at Sydenham Hill of the Crystal Palace, originally erected at the world exhibition of 1851. In the surrounding park, life-sized, painted, concrete statues of extinct animals were placed, which were designed by Benjamin Waterhouse Hawkins under the direction of Richard Owen. Among them were three models of an ichthyosaur. Although it was known that ichthyosaurs had been animals of the open seas, they were shown basking on the shore, a convention followed by many nineteenth century illustrations with the aim, as Conybeare once explained, of better exposing their build. This led to the misunderstanding that they really had an amphibious lifestyle. The pools in the park were at the time subjected to tidal changes, so that fluctuations in the water level at intervals submerged the ichthyosaur statues, adding a certain realism. Remarkably, internal skeletal structures, such as the scleral rings and the many phalanges of the flippers, were shown at the outside.
Later 19th-century finds
During the nineteenth century, the number of described ichthyosaur genera gradually increased. New finds allowed for a better understanding of their anatomy. Owen had noted that many fossils showed a downward bend in the rear tail. At first, he explained this as a post mortem effect, a tendon pulling the tail end downwards after death. However, after an article on the subject by Philip Grey Egerton,[25] Owen considered the possibility that the oblique section could have supported the lower lobe of a tail fin.[26] This hypothesis was confirmed by new finds from Germany. In the Posidonia Shale at Holzmaden, dating from the early Jurassic, already in the early nineteenth century, the first ichthyosaur skeletons had been found.[27][28][29] During the latter half of the century, the rate of discovery quickly increased to a few hundred each year. Ultimately, over four thousand were uncovered, forming the bulk of ichthyosaur specimens displayed today. The sites were also a Konservat-Lagerstätte, meaning not only the quantity, but also the quality was exceptional. The skeletons were very complete and often preserved soft tissues, including tail and dorsal fins. Additionally, female individuals were discovered with embryos.[30]
20th century
In the early twentieth century, ichthyosaur research was dominated by the German paleontologist Friedrich von Huene, who wrote an extensive series of articles, taking advantage of an easy access to the many specimens found in his country. The amount of anatomical data was hereby vastly increased.[31] Von Huene also travelled widely abroad, describing many fossils from locations outside of Europe. During the 20th century, North America became an important source of new fossils. In 1905, the Saurian Expedition led by John Campbell Merriam and financed by Annie Montague Alexander, found twenty-five specimens in central Nevada, which were under a shallow ocean during the Triassic. Several of these are now in the collection of the University of California Museum of Paleontology.
After a slack during the middle of the century, with no new genera being named between the 1930s and the 1970s, the rate of discoveries picked up towards its end. Other specimens are embedded in the rock and visible at Berlin–Ichthyosaur State Park in Nye County. In 1977 the 17-metre-long (56 ft) Triassic ichthyosaur Shonisaurus became the state fossil of Nevada. About half of the ichthyosaur genera today seen as valid were described after 1990. In 1992 Canadian paleontologist Elizabeth Nicholls uncovered the largest known specimen, a 23-metre-long (75 ft) Shastasaurus. The new finds have allowed a gradual improvement in knowledge about the anatomy and physiology of what had already been seen as rather advanced "Mesozoic dolphins". Christopher McGowan published a larger number of articles and also brought the group to the attention of the general public.[32] The new method of cladistics provided a means to exactly calculate the relationships between groups of animals, and in 1999, Ryosuke Motani published the first extensive study on ichthyosaur phylogenetics.[33] In 2003, McGowan and Motani published the first modern textbook on the Ichthyosauria and their closest relatives.[34]
Origin
The origin of the ichthyosaurs is contentious. Until recently, clear transitional forms with land-dwelling vertebrate groups had not yet been found, the earliest known species of the ichthyosaur lineage being already fully aquatic. In 2014, a small basal ichthyosauriform from the upper Lower Triassic was described that had been discovered in China with characteristics suggesting an amphibious lifestyle.[35] In 1937, Friedrich von Huene even hypothesised that ichthyosaurs were not reptiles, but instead represented a lineage separately developed from amphibians.[36] Today, this notion has been discarded and a consensus exists that ichthyosaurs are amniote tetrapods, having descended from terrestrial egg-laying amniotes during the late Permian or the earliest Triassic. However, establishing their position within the amniote evolutionary tree has proven difficult, due to their heavily derived morphology obscuring their ancestry.[37] Several conflicting hypotheses have been posited on the subject. In the second half of the 20th century, ichthyosaurs were usually assumed to be of the Anapsida, seen as an early branch of "primitive" reptiles.[38] This would explain the early appearance of ichthyosaurs in the fossil record, and also their lack of clear affinities with other reptile groups, as anapsids were supposed to be little specialised.[37] This hypothesis has become unpopular for being inherently vague because Anapsida is an unnatural, paraphyletic group. Modern exact quantitative cladistic analyses consistently indicate that ichthyosaurs are members of the clade Diapsida. Some studies showed a basal, or low, position in the diapsid tree.[39] More analyses result in their being Neodiapsida, a derived diapsid subgroup.[40]
Since the 1980s, a close relationship was assumed between the Ichthyosauria and the Sauropterygia, another marine reptile group, within an overarching Euryapsida, with one such study in 1997 by John Merck showing them to be monophyletic archosauromorph euryapsids.[41] This has been contested over the years, with the Euryapsida being seen as an unnatural polyphyletic assemblage of reptiles that happen to share some adaptations to a swimming lifestyle. However, more recent studies have shown further support for a monophyletic clade between Ichthyosauromorpha, Sauropterygia, and Thalattosauria as a massive marine clade of aquatic archosauromorphs originating in the Late Permian and diversifying in the Early Triassic.[42][43][44]
Affinity with the Hupehsuchia
Since 1959, a second enigmatic group of ancient sea reptiles is known, the Hupehsuchia. Like the Ichthyopterygia, the Hupehsuchia have pointed snouts and show polydactyly, the possession of more than five fingers or toes. Their limbs more resemble those of land animals, making them appear as a transitional form between these and ichthyosaurs. Initially, this possibility was largely neglected because the Hupehsuchia have a fundamentally different form of propulsion, with an extremely stiffened trunk. The similarities were explained as a case of convergent evolution. Furthermore, the descent of the Hupehsuchia is no less obscure, meaning a possible close relationship would hardly clarify the general evolutionary position of the ichthyosaurs.
In 2014, Cartorhynchus was announced, a small species with a short snout, large flippers, and a stiff trunk. Its lifestyle might have been amphibious. Motani found it to be more basal than the Ichthyopterygia and named an encompassing clade Ichthyosauriformes. The latter group was combined with the Hupesuchia into the Ichthyosauromorpha. The ichthyosauromorphs were found to be diapsids.[45]
The proposed relationships are shown by this cladogram:
Ichthyosauromorpha | |
Early Ichthyopterygia
The earliest ichthyosaurs are known from the Early and Early-Middle (Olenekian and Anisian) Triassic strata of Canada, China, Japan, and Spitsbergen in Norway, being up to 246 million years old. These first forms included the genera Chaohusaurus, Grippia, and Utatsusaurus. Even older fossils shows they were around 250 million years ago, just two million years after the Permian mass extinction. This early diversity suggests an even earlier origin, possibly late Permian.[46] They more resembled finned lizards than the fishes or dolphins to which the later, more familiar species were similar. Their bodies were elongated and they probably used an anguilliform locomotion, swimming by undulations of the entire trunk. Like land animals, their pectoral girdles and pelves were robustly built, and their vertebrae still possessed the usual interlocking processes to support the body against the force of gravity. However, they were already rather advanced in having limbs that had been completely transformed into flippers. They also were probably warm-blooded and viviparous.
These very early "proto-ichthyosaurs" had such a distinctive build compared to "ichthyosaurs proper" that Motani excluded them from the Ichthyosauria and placed them in a basal position in a larger clade, the Ichthyopterygia.[40] However, this solution was not adopted by all researchers.
Later Triassic forms
The basal forms quickly gave rise to ichthyosaurs in the narrow sense sometime around the boundary between the Early Triassic and Middle Triassic; the earliest Ichthyosauria in the sense Motani gave to the concept, appear about 245 million years ago. These later diversified into a variety of forms, including the still sea serpent-like Cymbospondylus, a problematic form which reached ten metres in length, and smaller, more typical forms like Mixosaurus. The Mixosauria were already very fish-like with a pointed skull, a shorter trunk, a more vertical tail fin, a dorsal fin, and short flippers containing many phalanges. The sister group of the Mixosauria were the more advanced Merriamosauria. By the Late Triassic, merriamosaurs consisted of both the large, classic Shastasauria and more advanced, "dolphin-like" Euichthyosauria. Experts disagree over whether these represent an evolutionary continuum, with the less specialised shastosaurs a paraphyletic grade that was evolving into the more advanced forms,[47] or whether the two were separate clades that evolved from a common ancestor earlier on.[48] Euichthyosauria possessed more narrow front flippers, with a reduced number of fingers. Basal euichthyosaurs were Californosaurus and Toretocnemus. A more derived branch were the Parvipelvia, with a reduced pelvis, basal forms of which are Hudsonelpidia and Macgowania.
During the Carnian and Norian, Shastosauria reached huge sizes. Shonisaurus popularis, known from a number of specimens from the Carnian of Nevada, was 15 m (49 ft) long. Norian Shonisauridae are known from both sides of the Pacific. Himalayasaurus tibetensis and Tibetosaurus (probably a synonym) have been found in Tibet. These large (10- to 15-m-long) ichthyosaurs have by some been placed into the genus Shonisaurus.[49] The gigantic Shonisaurus sikanniensis (considered as a shastasaurus between 2011 and 2013) whose remains were found in the Pardonet Formation of British Columbia by Elizabeth Nicholls, has been estimated to be as much as 21 m (69 ft) in length—if correct, the largest marine reptile known to date.
In the Late Triassic, ichthyosaurs attained the peak of their diversity. They occupied many ecological niches. Some were apex predators; others were hunters of small prey. Several species perhaps specialised in suction feeding or were ram feeders; also, durophagous forms are known. Towards the end of the Late Triassic, a decline of variability seems to have occurred. The giant species seemed to have disappeared at the end of the Norian. Rhaetian (latest Triassic) ichthyosaurs are known from England, and these are very similar to those of the Early Jurassic. A possible explanation is an increased competition by sharks, Teleostei, and the first Plesiosauria. Like the dinosaurs, the ichthyosaurs and their contemporaries, the plesiosaurs, survived the Triassic–Jurassic extinction event, and quickly diversified again to fill the vacant ecological niches of the early Jurassic.
Jurassic
During the Early Jurassic, the ichthyosaurs still showed a large variety of species, ranging from 1 to 10 m (3 to 33 ft) in length. Many well-preserved specimens from England and Germany date to this time and well-known genera include Eurhinosaurus, Ichthyosaurus, Leptonectes, Stenopterygius, and the large predator Temnodontosaurus. More basal parvipelvians like Suevoleviathan were also present. The general morphological variability had been strongly reduced, however.[50] Giant forms, suction feeders and durophagous species were absent.[51] Many of these genera possessed streamlined, dolphin-like thunniform bodies, although more basal clades like Eurhinosauria, which include Leptonectes and Eurhinosaurus, had longer bodies and long snouts.
Few ichthyosaur fossils are known from the Middle Jurassic. This might be a result of the poor fossil record in general of this epoch. The strata of the Late Jurassic seem to indicate that a further decrease in diversity had taken place. From the Middle Jurassic onwards, almost all ichthyosaurs belonged to the thunnosaurian clade Ophthalmosauridae. Represented by the 4 m-long (13 ft) Ophthalmosaurus and related genera, they were very similar in general build to Ichthyosaurus. The eyes of Ophthalmosaurus were huge, and these animals likely hunted in dim and deep water.[52] However, new finds from the Cretaceous indicate that ichthyosaur diversity in the Late Jurassic must have been underestimated.
Cretaceous
Traditionally, ichthyosaurs were seen as decreasing in diversity even further with the Cretaceous, though they had a worldwide distribution. All fossils from this period were referred to a single genus: Platypterygius. This last ichthyosaur genus was thought to have become extinct early in the late Cretaceous, during the Cenomanian about 95 million years ago, much earlier than other large Mesozoic reptile groups that survived until the very end of the Cretaceous. Two major explanations have been proposed for this extinction including either chance or competition from other large marine predators such as plesiosaurs. The overspecialisation of ichthyosaurs may be a contributing factor to their extinction, possibly being unable to 'keep up' with fast teleost fish, which had become dominant at this time, against which the sit-and-wait ambush strategies of the mosasauroids proved superior.[53] This model thus emphasised evolutionary stagnation, the only innovation shown by Platypterygius being its ten fingers.[54]
Recent studies, however, show that ichthyosaurs were actually far more diverse in the Cretaceous than previously thought. Fragments previously referred to "Platypterygius" have been found to be from several different taxa. As of 2012, at least eight lineages are known to have spanned the Jurassic-Cretaceous boundary including Acamptonectes, Sveltonectes, Caypullisaurus, and Maiaspondylus.[55] In 2013, a Cretaceous basal thunnosaurian was revealed: Malawania.[56] Indeed, likely a radiation during the Early Cretaceous occurred due to an increase of coastlines when the continents further broke up.[57]
The demise of the ichthyosaurs has been described as a two-step process.[58] A first extinction event in the beginning of the Cenomanian eliminated two of the three ichthyosaur feeding guilds still present: the 'soft-prey specialists' and the 'generalists', leaving only an unspecialized apex predator group.[58] The second extinction event took place during the Cenomanian-Turonian boundary event, a marine 'anoxic event', after which just a single lineage survived, Platypterygius hercynicus, which then disappeared about 93 million years ago.[59] Ichthyosaur extinction was thus a pair of abrupt events rather than a long decline, probably related to the environmental upheavals and climatic changes in the Cenomanian and Turonian.[58][60] Competition with early mosasaurs is unlikely to have been a contributing factor since large mosasaurs did not appear until 3 million years after the ichthyosaur extinction, filling the resulting ecological void left by the extinction of ichthyosaurs.[58] Plesiosaurian polycoltylids perhaps also filled some of the niches previously occupied by ichthyosaurs, although they had coexisted for 19 million years. The extinction was most likely the result of ecological change and volatility that caused changes in migration, food availability, and birthing grounds. This part of the Cretaceous was one in which many other marine extinctions occurred, including those of some types of microplankton, ammonites, belemnites, and reef-building bivalves.[58]
In modern phylogeny, clades are defined that contain all species forming a certain branch of the evolutionary tree. This also allows one to clearly indicate all relationships between the several subgroups in a cladogram. In 1999, a node clade Ichthyopterygia was defined by Motani as the group consisting of the last common ancestor of Ichthyosaurus communis, Utatsusaurus hataii and Parvinatator wapitiensis; and all its descendants. Within Motani's phylogeny, the Ichthyopterygia were the larger parent clade of a smaller stem clade Ichthyosauria that was defined as the group consisting of Ichthyosaurus communis and all species more closely related to Ichthyosaurus than to Grippia longirostris.[33] Motani's concept of the Ichthyosauria was thus more limited than the traditional one that also contained basal forms, such as Grippia, Utatsusaurus, and Parvinatator.
The following cladogram is based on Motani (1999):[33]
An alternative terminology was proposed by Maisch & Matzke in 2000, trying to preserve the traditional, more encompassing content of the concept Ichthyosauria. They defined a node clade Ichthyosauria as the group consisting of the last common ancestor of Thaisaurus chonglakmanii, Utatsusaurus hataii, and Ophthalmosaurus icenicus, and all its descendants.[61] Ichthyosauria sensu Motani might materially be identical to a clade that Maisch & Matzke in 2000 called Hueneosauria, depending on the actual relationships.
Cladogram based on Maisch and Matzke (2000)[61] and Maisch and Matzke (2003)[62] with clade names following Maisch (2010):[37]
Ichthyosauria | |