Pliosaurus

''Pliosaurus'' (meaning 'more lizard') is an extinct genus of thalassophonean pliosaurid known from the Kimmeridgian and Tithonian stages (Late Jurassic) of Europe and South America. Their diet would have included fish, cephalopods, and marine reptiles. This genus has contained many species in the past but recent reviews found only six (''P. brachydeirus'', ''P. carpenteri'', ''P. funkei'', ''P. kevani'', ''P. rossicus'' and ''P. westburyensis'') to be valid, while the validity of two additional species awaits a petition to the International Code of Zoological Nomenclature. Currently, ''P. brachyspondylus'' and ''P. macromerus'' are considered dubious, while ''P. portentificus'' is considered undiagnostic. Most species of ''Pliosaurus'' reached in length and in body mass, while ''P. rossicus'' and ''P. funkei'' may have reached or even exceeded in length and in body mass, being the largest plesiosaurs of all time. Species of this genus are differentiated from other pliosaurids based on seven autapomorphies, including teeth that are triangular in cross section.

Discovery and species

''Pliosaurus brachydeirus''

''Pliosaurus brachydeirus'' is the type species of the genus. It was first described and named by the English paleontologist Richard Owen in 1841, as a species of the wastebasket taxon ''Plesiosaurus'' in its own subgenus ''Pleiosaurus'', creating ''Plesiosaurus (Pleiosaurus) brachydeirus''. Later that year or in 1842, Owen published another study in which the species was relocated to its own genus, which he misspelled as ''Pliosaurus''. As have been noted by several authors, ''Plesiosaurus (Pleiosaurus)'' is the original spelling of ''Pliosaurus'', and therefore according to Article 32 of the ICZN, ''Pleiosaurus'' is the correct spelling of the generic name as well. However, because this spelling had been abandoned since Phillips (1871), ''Pliosaurus'' should be preserved according to Article 33.3.1 of the ICZN. The generic name is derived from πλειων, ''pleion'', meaning "more" and , ''sauros'', meaning "lizard" in Ancient Greek, in reference to Owen' belief that ''Pliosaurus'' was more closely related to "saurians" (including crocodilians) than ''Plesiosaurus'' was. The etymology of the specific name was not specified, but it probably refers to the shorter teeth of ''P. brachydeirus'' compared to teeth of other species then referred to ''Plesiosaurus''. The specific name has occasionally erroneously been spelled as ''brachydirus'', for example by Richard Lydekker (1889a, 1889b).

''P. brachydeirus'' is known from the holotype which includes seven specimens found in association and housed at Oxford University Museum of Natural History, OUMNH J.9245, OUMNH J.9247 through OUMNH J.9301 and OUMNH J.10453. The specimen consists of a partial skull and lower jaw, several axial elements and limb material. Other specimens that are referable to this species include OUMNH J.9285, and OUMNH J.9192 through OUMNH J.9301, all described by Owen (1841–1842) and were found associated with the holotype. The specimens were collected by Prof. William Buckland at Market Rasen, Lincolnshire, from the ''Rasenia cymodoce'' ammonite zone of the lower Kimmeridge Clay Formation, dating to the early Kimmeridgian stage.

Knutsen (2012) revised the validity of this species and was able to diagnose it on a basis of combination of traits. ''P. brachydeirus'' had approximately 70 teeth in the lower jaw (72 according to Benson ''et al.'' (2013)), 8-9 or more pairs of symphyseal teeth in dorsal view (12 pairs according to Benson ''et al.'' (2013)) and 5 or more premaxillary teeth. It shows "type III" retroarticular process and autapomorphic (unique) traits of the cervical vertebrae, which had a smooth ventral surface and a ventral keel, unlike rounded to flat ventral surface seen in other species. Benson ''et al.'' (2013) also noted that it lacks anisodont premaxillary dentition. The ontogenetic stage of the holotype of ''P. brachydeirus'' is not known, but the rounded edge on the distal end of the femur and lack of separation between the femoral capitulum and trochanter suggests that it is from a relatively young individual. According to Benson ''et al.'' (2013), the flat morphology of the proximal surface of the radius or tibia also suggests that it is a juvenile.

''Pliosaurus carpenteri''

''P. carpenteri'' is known solely from the holotype BRSMG Cd6172, a nearly complete long skull, mandible and postcranial skeleton, including at least 17 complete vertebrae housed at Bristol City Museum and Art Gallery, Bristol, England. The specimen was collected at the Westbury Clay pit, Wiltshire, from subdivision E4 of the ''Aulacostephanus eudoxus'' ammonite zone, seven metres below the Crussoliceras Limestone of the Kimmeridge Clay Formation, dating to the late Kimmeridgian. Nicknamed "Westbury pliosaur II", it was first described by Sassoon ''et al.'' (2012) who, together with Knutsen (2012), assigned it tentatively to ''Pliosaurus sp.''. It was reassigned to its own species by Roger B. J. Benson, Mark Evans, Adam S. Smith, Judyth Sassoon, Scott Moore-Faye, Hilary F. Ketchum and Richard Forrest in 2013. The specific name honors Simon Carpenter, the discoverer and collector of BRSMG Cd6172.

Sassoon ''et al.'' (2012) originally ascribed the differences between BRSMG Cc332 (the holotype of ''P. westburyensis'') and BRSMG Cd6172 to intraspecific variation, with these specimens possibly being sexual dimorphs, due to fact that both were collected from close stratigraphic levels of the same quarry. However, Benson ''et al.'' (2013) showed that the differences between them are relatively great even in the context of specimens from other localities. They diagnosed ''P. carpenteri'' based on a single autapomorphy – unlike all other thalassophoneans other than the proposed neotype of ''P. brachyspondylus'', the dorsal surface of the surangular lacks any fossa, and in contrast to all other specimens of ''Pliosaurus'' faces dorsally, not inclined to face dorsolaterally. ''P. carpenteri'' also possesses a unique combination of characters, including: low dentary alveolar count including only 18 postsymphysial alveoli, and a total count of 27; intermediate low count of syphysial alveoli including only 9; teeth fully trihedral, possessing a flat, anteroposteriorly broad labial surface lacking enamel ridges; mediolateral expansion of caniniform regions of the premaxilla and maxilla relatively pronounced, although this might be due to crushing; six closely spaced premaxillary alveoli; anisodont premaxillary dentition; diastema present between maxillary and premaxillary alveolar rows; premaxilla–parietal suture located level with the anterior region of the orbit; cervical centra lacking ventral ridge; and epipodials with highly convex proximal surfaces.

''Pliosaurus funkei''

''P. funkei'' is known from two partial skeletons, the holotype PMO 214.135 and the referred PMO 214.136, from the Svalbard archipelago of Norway. Housed at the University of Oslo Natural History Museum, the skeletons were found south of Sassenfjorden, from the southeast side of Mount Knerten, in the Arctic Spitsbergen island. Both individuals were collected by a Norwegian team led by Dr. Jørn Hurum within of one another, approximately below the Myklegardfjellet Bed from the black shales of the Slottsmøya Member, which is the uppermost out of four named members in the Agardhfjellet Formation. This stratigraphic horizon belongs to the ''Dorsoplanites ilovaiskyi'' to ''Dorsoplanites maximus'' ammonite zones (probably to the latter), of the middle Volgian stage which correlates with the middle Tithonian stage. The skeletons were discovered during eight seasons of fieldwork (2004–2012 field seasons) in the Slottsmøya Member, that have yielded other skeletal remains of marine reptiles, including the plesiosauroids '' Colymbosaurus svalbardensis'', '' Djupedalia'' and '' Spitrasaurus'', and the ichthyosaurs ''Cryopterygius'' and '' Palvennia''. ''P. funkei'' was first described and named by Espen M. Knutsen, Patrick S. Druckenmiller and Jørn H. Hurum in 2012. The specific name honors Bjørn Funke, the discoverer of the holotype, and his wife May-Liss Knudsen Funke for volunteering in the paleontological collections at the Museum.Low resolution pdf
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The holotype of ''P. funkei'' is represented by the anterior portions of the upper and lower jaws (including premaxillary and dentary teeth), one nearly complete cervical centrum and two partial cervical centra, three pectoral centra with neural arches, fifteen dorsal centra and eight neural arches, a complete right coracoid, numerous rib fragments and gastralia, and a complete right forelimb. The referred specimen is represented by five partial cervical centra, one partial dorsal centrum, and a partial skull including the occipital condyle, a complete left quadrate, a partial left squamosal and incomplete left surangular and articular. Several fragmentary and unidentified bones also pertain to PMO 214.136. Due to the Arctic climate of Svalbard, the specimens were subjected to repeated freeze-thaw cycles before collection, extensively fracturing and degrading the material. PMO 214.136 was discovered in 2007, following the collection of approximately 20,000 fragments that compose PMO 214.135 which were found moist in situ and degraded upon drying during the preparation process (individual fragments are catalogued at the University of Oslo Natural History Museum by specimen number followed by a slash and a number). Estimates of skull length are approximately for the holotype and for PMO 214.136, suggesting a total body length of for the species, making ''P. funkei'' one of the largest pliosaurs described so far. Due to its large size and relative completeness, the species, nicknamed "Predator X" before its formal description, gained extensive media coverage, which claimed that it was "most fearsome animal ever to swim in the oceans". Morphological and histological characters, such as the presence of a tuberosity on the humerus and a well developed anterior process on the coracoid, and abnormal hardening and increase in density of bone, indicate that both specimens were adult individuals. Even though none of the neural arches are fused to their centra in the vertebral column of both individuals (a possible juvenile trait), this feature is present in all large pliosaurids, and thus possibly paedomorphic within Pliosauridae.

Knutsen ''et al.'' (2012) diagnosed the species based on a unique combination of characters of the holotype. ''P. funkei'' has a possibly unique "type I" retroarticular process, unlike ''P. brachydeirus'', ''P. brachyspondylus'' and ''P. macromerus''. Unlike ''P. brachydeirus'', its cervical centra possess a rugose ventral surface, but lack ventral keel. Finally, it possesses comparatively longer forelimbs than other known pliosaurids, with a long humerus, more than 7 times the average width of cervical vertebral centra, in comparison to ''P. brachyspondylus'' and ''P. rossicus'', which have humeri less than 4.5 times the cervical width. Its complete teeth count is not known, however, it has at least six pairs of teeth in the mandibular symphysis, and at least five premaxillary tooth pairs. The two known individuals of ''P. funkei'' preserve mostly different regions of the skeleton and overlap only by cervical vertebrae. Nevertheless, these cervical vertebrae are morphologically indistinguishable, and both individuals were found in proximity to one another, at exactly the same stratigraphic horizon of the Slottsmøya member, strongly supporting the referral of PMO 214.136 to ''P. funkei''. Knutsen ''et al.'' (2012) suggested that ''P. funkei'' is more similar to ''P. rossicus'' and the proposed neotype of ''P. macromerus'' than to ''P. brachydeirus'' and the proposed neotype of ''P. brachyspondylus'' in its cranial morphology.

Analysis of bones from the four flippers suggest that the animal cruised using only the fore-flippers, using the back flippers for extra speed when pursuing and capturing prey.

Predator X's brain was of a similar type and size, proportionally, to that of today's great white shark, the team says.

A television programme entitled '' Predator X'' first aired on History in 2009. It was also featured in the fourth episode of the BBC documentary series '' Planet Dinosaur'' in 2011, where it is shown hunting '' Kimmerosaurus'', a smaller plesiosaur. The scene is based on damages to the one known skull of ''Kimmerosaurus'', showing damage consistent with an attack of a very large animal with ''Liopleurodon''-like dentition.

''Pliosaurus kevani''

''P. kevani'' is known solely from the holotype DORCM G.13,675, a nearly complete long skull and mandible housed at Dorset County Museum, Dorchester, England. The specimen was collected at Wyke Siltstone bed of Osmington Bay, from the ''Rasenia cymodoce'' ammonite zone, Kimmeridge Clay Formation of the Ancholme Group, dating to the early Kimmeridgian. DORCM G.13,675 was collected over a period of eight years as pieces up to in mass weathered out of the sea-cliff of Black Head. Most pieces were collected from loose or fallen blocks without any permits required, while other parts were collected in situ and purchased from land owners. They were first identified as a pliosaurid skull by Richard Edmonds, Earth Sciences Manager for Dorset and East Devon Coast World Heritage Site Team. Due to its large size and completeness, the specimen gained extensive media coverage, and its acquisition was announced publicly in October 2009. Additional elements were later donated by Patrick Clarke and purchased from Shirley Swaine. DORCM G.13,675 went on display in Dorchester County Museum in July 2011, after being in preparation between March 2010 and March 2011. Preparation of the lower jaws took 200 hours and a further 365 hours were needed to complete preparation of the skull. ''P. kevani'' was first described and named by Roger B. J. Benson, Mark Evans, Adam S. Smith, Judyth Sassoon, Scott Moore-Faye, Hilary F. Ketchum and Richard Forrest in 2013. The specific name honors Kevan Sheehan, the owner of a small café overlooking the sea at Osmington Mills, who collected most of the holotype during daily walks along the foreshore.

Benson ''et al.'' (2013) diagnosed the species based on four autapomorphies of the holotype. The subrectangular sheet of the maxilla extends anteriorly on alveolar surface of the premaxilla to contact the distalmost premaxillary alveolus, while in other species of ''Pliosaurus'' an interdigitating premaxilla-maxilla suture is located midway between the mesialmost maxillary and distalmost premaxillary alveoli. Its pineal foramen is surrounded by a raised rim, while other thalassophoneans have a shallow fossa containing anteroposteriorly oriented grooves or ridges, that extends anteriorly from the pineal foramen. The mesial postsymphysial dentary alveoli are everted to face dorsolaterally, and not dorsally as seen in other species. Finally, the lateral surface of the mandible dorsoventrally concave posteriorly, while other thalassophoneans show flat or weakly convex lateral surface of the postedentary bones. ''P. kevani'' also possesses a unique combination of characters, including: high dentary alveolar count including 22 postsymphysial alveoli and an estimated total count of 36–37; high count of symphysial dentary alveoli including at least 7, estimated as 14–15; subtrihedral teeth, possessing a suboval cross-section with slightly flattened labial surface bearing only thinly distributed enamel ridges; pronounced mediolateral expansion of caniniform regions of the premaxilla and maxilla; six closely spaced premaxillary alveoli; anisodont premaxillary dentition; and premaxilla–parietal suture located level with the anterior region of the orbit.

CAMSM J.35990, a complete postcranial skeleton originally referred to ''Stretosaurus macromerus'', and later to ''Pliosaurus sp.'', might also pertain to ''P. kevani''. Although non-diagnostic at the species level, Benson ''et al.'' (2013) differentiated it from most specimens of ''Pliosaurus'' based on its subtrihedral teeth, which are otherwise present only in ''Pliosaurus kevani'', and possibly also in ''Gallardosaurus iturraldei'' from the Oxfordian of Cuba. Even though it shares with the holotype of ''P. kevani'' a very large body size and stratigraphically closer to it, otherwise the specimens cannot be directly compared. Therefore, it was tentatively referred to as ''Pliosaurus'' cf. ''kevani''. A subtrihedral tooth from the Kimmeridge Clay of Ely, LEICT G418.1965.108, is also referred to ''Pliosaurus'' cf. ''kevani'' based on similar arguments.

''Pliosaurus rossicus''

''P. rossicus'' was first described and named by Nestor Ivanovich Novozhilov in 1948. The specific name is derived from the name of Russia, where the holotype was found. The holotype of ''P. rossicus'', PIN 304/1 housed at Paleontological Institute, Russian Academy of Sciences, consists of cranial and some postcranial remains of a relatively small pliosaur. It was collected at the right bank of the Volga River, of Chuvashia, European part of Russia, from the Buinsk Mine oil shales, ''Dorsoplanites panderi'' ammonite zone, dating to the middle Volgian stage (also known as middle Tithonian). Novozhilov (1964) later also described some pectoral remains associated with the holotype. The holotype preserved trihedral teeth like other members of ''Pliosaurus'', and bears 6 tooth pairs in the mandibular symphysis, similar to OUMNH J.10454. Halstead (1971) reassigned this species to ''Liopleurodon'' based on this symphyseal tooth count, but Knutsen (2012) and Benson ''et al.'' (2013) referred it back to ''Pliosaurus'', as it exhibits the diagnostic traits of the genus such as trihedral teeth. PIN 304/1 has also been interpreted as a juvenile by both Halstead (1971) and Storrs ''et al.'' (2000) based on its relatively small size and poorly developed dorsal blade and anteroventral ramus of the scapula.

Halstead (1971) referred a second, larger specimen PIN 2440/1 consisting of a partial rostrum and hind limb, to ''P. rossicus''. PIN 2440/1 was originally described as ''Pliosaurus'' cf. ''grandis'' by Rozhdestvenskii (1947), but later referred to ''P. rossicus'' based on the presence of a similar number of mandibular symphyseal teeth with the holotye and their relative stratigraphic co-occurrence. Another specimen of large pliosaur was tentatively assigned to ''P. rossicus'' by Malakhov (1999). The specimen was collected from the lower Volgian (early Tithonian) of Kazakhstan, and represents postcranial remains No. 13-1958, at Institute of Zoology MS-AS RK.

Knutsen (2012) suggested possible synonymy between ''P. macromerus'' and ''P. rossicus'' based on the presence of only six symphysial and five premaxillary alveoli in both. Nevertheless, he provisionally retained ''P. rossicus'' as a separate species, as the stratigraphic ranges of the two taxa do not overlap, and the specimens were not adequate described. However, a reexamination of NHMUK PV OR 39362 (proposed neotype of ''P. macromerus'') by Benson ''et al.'' (2013), revealed that it had at least seven symphyseal tooth, but more likely nine. Therefore, they considered ''P. rossicus'' to be a valid species of ''Pliosaurus'' based on the presence of an autapomorphic short symphysis containing only six alveoli. Based on the presence of this trait, they tentatively referred OUMNH J.10454 (and thus possibly OUMNH J.50376 and OUMNH J.50377) to ''P. ? rossicus''. These specimens were all collected at Chawley brick pit, of the upper part of the Lower Kimmeridge Clay, dating to the late Kimmeridgian, and were originally assigned to ''P. macromerus''. OXFUM J.10454 is a highly reconstructed and fragmentary specimen, with a total length of . Tarlo estimated that the skull length of this individual had originally been more than , however Benson ''et al.'' (2013) argued that this cannot be currently determined. Apart from the autapomorphy noted above and trihedral teeth, ''P. rossicus'' possesses the following combination of characters (based on its holotype): 5 premaxillary tooth pairs; cervical vertebrae with ornamented ventral surface, but lacking ventral keel; proportionally shorter humeri than ''P. funkei'', less than 4.5 times the average width of cervical centra, versus more than 7 times.

''Pliosaurus westburyensis''

''P. westburyensis'' is known solely from the holotype BRSMG Cc332, a nearly complete skull and postcranial fragments, including four cervical vertebrae housed at Bristol City Museum and Art Gallery, Bristol. The specimen was collected at the Westbury Clay pit, Wiltshire, England, from subdivision E5 of the ''Aulacostephanus eudoxus'' ammonite zone, one metre below the Crussoliceras Limestone of the Kimmeridge Clay Formation, dating to the late Kimmeridgian. Nicknamed "Westbury pliosaur I", it was first described by Taylor & Cruickshank (1993) and referred to ''P. brachyspondylus'' based on the absence of a ventral keel on the cervical vertebral centra. BRSMG Cc332 was assigned tentatively to ''Pliosaurus sp.'' by Sassoon ''et al.'' (2012) and Knutsen (2012) and reassigned to its own species by Roger B. J. Benson, Mark Evans, Adam S. Smith, Judyth Sassoon, Scott Moore-Faye, Hilary F. Ketchum and Richard Forrest in 2013. The specific name honours the town of Westbury near which the holotype was found.

The mandible of BRSMG Cc332 is approximately 50 cm longer than CAMSM J.35991 (proposed neotype for ''P. brachyspondylus''), but is shorter than the two French specimens referred to ''P. brachyspondylus''. Knutsen (2012) distinguished BRSMG Cc332 from ''P. brachyspondylus'' as the former has a "type IV" retroarticular process and a much lower degree of fusion between the anterior mandibular bones. Benson ''et al.'' (2013) diagnosed the species based on three autapomorphies. ''P. westburyensis'' has widely spaced premaxillary alveoli, with interalveolar walls approximately half the anteroposterior length of a single alveolus. It also has a long, sheet-like process of the maxilla that extends back to the anterolateral part of the maxilla–frontal contact medial to the external naris, and terminates just anterior to midlength of the orbital. Finally, the suture between the premaxilla and parietal bone is located around orbital midlength. ''P. westburyensis'' also possesses a unique combination of characters, including: low dentary alveolar count including only 18 postsymphysial alveoli; teeth fully trihedral in cross-section, possessing a flat, anteroposteriorly broad labial surface lacking enamel ridges; relatively slight mediolateral expansion of premaxilla and maxillary caniniform region; six premaxillary alveoli; lack of anisodont premaxillary dentition; lack of diastema between maxillary and premaxillary alveolar rows; and cervical centra lacking ventral ridge.

Other species

''Pliosaurus brachyspondylus''

''Pliosaurus brachyspondylus'' was first described and named by Owen in 1839, as a species of ''Plesiosaurus''. The specific name is derived from βραχυς, ''brachus'', meaning "short" and σπόνδυλος, ''spondylos'', meaning "vertebra" in Ancient Greek. It was named on the basis of a series of unassociated cervical vertebrae as the holotype. These specimens were collected at Headington Pits near Oxford, Oxfordshire, England, from the Kimmeridge Clay. It was later noted by Pocock (1908), that the material was found in the lower part of the Kimmeridge Clay, as the pits expose the contact between the Kimmeridge Clay Formation and the underlying Corallian beds. Several other cervical centra from the same strata at Weymouth, Dorsetshire, that had been named ''Plesiosaurus giganteus'' by Conybeare (1824), were also referred to ''Plesiosaurus brachyspondylus'' by Owen (1839). Eichwald (1868) reassigned ''P. brachyspondylus'' to ''Pliosaurus'' but did not provide diagnosis to distinguished these vertebrae from those of the type species of the genus. ''P. giganteus'' was later synonymised by Lydekker (1889a) with ''P. brachydeirus'', the type species.

According to Tarlo (1959a), the holotypes of ''P. giganteus'' and ''P. brachyspondylus'' have been lost or destroyed since their initial descriptions. Therefore, he selected a single posterior cervical centrum, CAMSM J.29564, as the neotype of ''P. brachyspondylus'', while ''P. giganteus'' became a '' nomen oblitum'', forgotten name, as ''P. brachyspondylus'' had traditionally been given priority over it. This centrum was the only not dorsal centrum from a series of thirty associated centra listed by Harry Seeley (1869) as belonging to ''P. brachyspondylus''. They were collected at the Roswell (Roslyn) pit near Ely, Cambridgeshire, also in England, from between the ''Aulacostephanus mutabilis'' or ''Aulacostephanus eudoxus'' ammonite zones, of the lower Kimmeridge Clay Formation. Although the measurements of the neotype agree with these of the lost holotype, they are also similar to these of referred specimens of ''P. brachydeirus'' (OUMNH J.9291-9301) and '' "Pliosaurus" andrewsi'' ( R.1243, cast of mid-cervical centrum referred to ''P. evansi''). Additionally, Seeley's referral was based on a single character, "articular surface is very slightly concave, with a small round depression at the centre", a feature that is now known to be common in other pliosaurids as well. Thus, Tarlo's choice of the neotype of ''P. brachyspondylus'' relies solely on the similarity in size to the original material described by Owen (1839), which is also similar to ''P. brachydeirus''. The neotype centrum, CAMSM J.29564, differs from the holotype of ''P. brachydeirus'' in the following two traits; it has ventral surface ornamentation but lacks a ventral keel. Nevertheless, the neotype for ''P. brachyspondylus'' is non-diagnostic from other species of ''Pliosaurus'', and thus the name must be considered a '' nomen dubium''.

In the same paper, Tarlo (1959a) described an associated pliosaur skeleton, CAMSM J.35991, and referred it to ''P. brachyspondylus''. CAMSM J.35991 consists of a complete mandible, most of the axial skeleton and parts of the appendicular skeleton. It was found in 1889 in the ''Aulacostephanus eudoxus'' ammonite zone of the lower Kimmeridge Clay, at the same locality as CAMSM J.29564 (the neotype for ''P. brachyspondylus''). Knutsen (2012) suggested to replace the neotype for ''P. brachyspondylus'', with CAMSM J.35991 as the new neotype, because both specimens and possibly the lost holotype are from the same locality and horizon, and similar in size. CAMSM J.35991 is much more complete and can be distinguished from all other species of ''Pliosaurus''. Benson ''et al.'' (2013) agreed with this suggestion, but considered ''P. brachyspondylus'' to be Thalassophonea indet., until a petition to the ICZN is made. Based on CAMSM J.35991, Knutsen (2012) provisionally diagnosed ''P. brachyspondylus'' as a ''Pliosaurus'' with approximately 60 (58 according to Benson ''et al.'' (2013)) teeth in the lower jaw, 9 pairs of symphyseal teeth in dorsal view. It had "type II" retroarticular process and proportionally shorter humeri than ''P. funkei''. As also seen in CAMSM J.29564, it had cervical centra with ventral surface ornamentation, but lacking a ventral keel. According to Benson ''et al.'' (2013), the flat morphology of the proximal surface of the radius or tibia suggests that CAMSM J.35991 is a juvenile.

According to Knutsen (2012), Bardet ''et al.'' (1993) referred two additional mandibles to ''P. brachyspondylus'' based solely on a similar number of dentary and symphyseal teeth; BHN 2R.370, collected at the Moulin-Wibert quarry, from the ''Rasenia cymodoce'' ammonite zone of the Calcaires de Moulin-Wibert Formation of Nord-Pas-de-Calais, and MNHN cat.24.1 collected at Le Havre, Normandy, both from the early Kimmeridgian of France. Benson ''et al.'' (2013) discussed only BHN 2R.370 originally referred to ''Pliosaurus grandis'', stating that ''P. carpenteri'' has a similar count of dentary and symphysial teeth, and thus the specimen cannot be identified to species level. However it was referred to ''Pliosaurus'' indet. as it has a broad, dorsolaterally facing surangular fossa, bounded laterally by a fossa and ridge. Another specimen, BRSMG Cc332, was referred to ''P. brachyspondylus'' by Taylor and Cruickshank (1993) and to ''Pliosaurus sp.'' by Sassoon ''et al.'' (2012) and Knutsen (2012), but was reassigned to its own species ''P. westburyensis'' by Benson ''et al.'' (2013).

''Pliosaurus macromerus''

''Pliosaurus macromerus'' was first described and named by John Phillips in 1871, as a species of ''Pleiosaurus'', on the basis of a large femur, OUMNH J.12498, and a series of unassociated vertebrae. The specific name is derived from μακρός, ''makros'', meaning "long" in Ancient Greek and ''mēros'', meaning "thigh" in Latin, from Greek, in reference to the large size of OUMNH J.12498 (a thigh bone). These specimens were collected during the excavation of the Great Western Railway near Swindon, Wiltshire, probably from the ''Pectinatites hudlestoni'' and ''Pavlovia pallasioides'' ammonite zone, Upper Kimmeridge Clay, of the Swindon Clay and Cemetery Beds. Lydekker (1889a) amended the ''Pleiosaurus macromerus'' into ''Pliosaurus'', and reassigned NHMUK PV OR 39362 to this species with other material, based solely on large size. NHMUK PV OR 39362, a complete skull and mandible, was first described by Owen (1869) who referred it to ''Pliosaurus grandis''. It was collected at Kimmeridge Bay, Dorsetshire, from the ''Aulacostephanus autissidorensis'' or ''Pectinatites elegans'' ammonite zones of the Upper Kimmeridge Clay Formation, dating to the late Kimmeridgian or early Tithonian.

Tarlo (1959b) erected OUMNH J. 10441, one of the partial cervical vertebrae from the collection of unassociated remains listed by Philips (1871), as the lectotype of ''P. macromerus''. It was assigned to ''P. macromerus'' based on its large size, similar to those of ''P. westburyensis'' and ''P. funkei''. Tarlo (1959b) described the lectotype as "somewhat roughened", while Lydekker (1889a) described it as being "very coarse and rough" in reference to its ventral rugosity, resembling that of ''P. brachyspondylus''. Tarlo (1959b) also erected a new generic name for ''P. macromerus'', ''Stretosaurus'', due to the unusual scapular morphology of a specimen he described and referred to it, CAMSM J.35990. It was found at Stretham, southwest of Ely in Cambridgeshire, probably from the early Kimmeridgian ''Aulacostephanus mutabilis'' ammonite zone. It represents an associated fragmentary skull and a relatively complete postcranial skeleton. Tarlo (1959b) referred CAMSM J.35990, and two other very large, anterior cervical vertebral centra, CAMSM J.29562 and CAMSM J.30057, to ''Stretosaurus macromerus'' based on similar size and ornamentation of the cervical vertebrae. Knutsen (2012) noted that this ornamentation is shared with ''P. westburyensis'' and the proposed neotype of ''P. brachyspondylus''.

Based on similar number of mandibular symphyseal teeth with NHMUK PV OR 39362, Tarlo (1959b) also assigned to ''S. macromerus'' a partial mandible, OUMNH J.10454, represented by an anterior rostral tip and associated trihedral teeth. Nicknamed "Cumnor mandible", it was collected at Chawley brick pit, Oxfordshire, alongside '' Cumnoria prestwichii''. This locality most likely belongs to the ''Aulacostephanus eudoxus'' or ''A. autissidorensis'' ammonite zone, of the upper part of the Lower Kimmeridge Clay. Knutsen (2012) noted that there is no overlap between the cranial portions of CAMSM J.35990 and NHMUK PV OR 39362 or OUMNH J.10454. Halstead (1989) referred a more recently discovered, complete specimen (NHMUK R8928) to ''P. brachyspondylus'' based on its long mandibular symphysis. Using this specimen he re-identified the "scapula" of CAMSM J.35990 as an ilium, but in spite of their similar ilial morphology, reassigned ''S. macromerus'' to '' Liopleurodon''. According to Noè ''et al.'' (2004), the specimens of ''S. macromerus'' should be referred to ''P. macromerus'' as the name ''Stretosaurus'' is invalid, and NHMUK PV OR 39362 and CAMSM J.35990 exhibit the autapomorphic trihedral teeth of ''Pliosaurus''.

Knutsen (2012) suggested to replace the lectotype of ''P. macromerus'', with NHMUK PV OR 39362 as a neotype, because the lectotype (as well as the remaining syntypes) is indistinguishable from all species of ''Pliosaurus'', apart from ''P. brachydeirus'' due to vertebral ornamentation. NHMUK PV OR 39362 is much more complete and can be distinguished from all other species of ''Pliosaurus''. NHMUK PV OR 39362 has been traditionally assigned to ''P. macromerus'', and even though it has previously been assigned to ''P. grandis'', Lydekker (1889a) showed that there is no evidence that the syntypes of ''P. grandis'' even belong to ''Pliosaurus'', and there is no overlapping material between them and NHMUK PV OR 39362. Benson ''et al.'' (2013) agreed with the suggestion to assign a neotype of ''P. macromerus'', but considered it to be Thalassophonea indet., until a petition to the ICZN is made. Based on NHMUK PV OR 39362, Knutsen (2012) provisionally diagnosed ''P. brachyspondylus'' as a ''Pliosaurus'' with at least 50 teeth in the lower jaw (probably 54), at least 7 pairs (probably 9) of symphyseal teeth and 5 pairs of premaxillary teeth. It also has "type III" retroarticular process. Benson ''et al.'' (2013) noted that it lacks anisodont premaxillary dentition.

Other specimens previously referred to ''P. macromerus'' are currently assigned to other species of ''Pliosaurus'', rendering this species a '' nomen dubium''. Knutsen (2012) referred CAMSM J.35990 to ''Pliosaurus sp.'', stating that it is non-diagnostic at the species level. Benson ''et al.'' (2013) agreed that it cannot be confidently diagnosed as a distinct species, or referred to an existing species with certainty. Nevertheless, they differentiated CAMSM J.35990 from most specimens of ''Pliosaurus'' based on its subtrihedral teeth, which are otherwise present only in ''Pliosaurus kevani'', and possibly also in ''Gallardosaurus iturraldei'' from the Oxfordian of Cuba. Furthermore, it shares with ''P. kevani'' a very large body size and stratigraphically closer to ''P. kevani'', but cannot be otherwise compared to it. Therefore, it was tentatively referred to as ''Pliosaurus'' cf. ''kevani''. According to Knutsen (2012), OUMNH J.10454 is referable to ''P. macromerus'', together with two associated fragments, OUMNH J.50376 and OUMNH J.50377, each constituting one ramus of a lower jaw from a single individual. All three specimens were collected from the same pit, are of similar size, and have "type III" retroarticular process. The referral to ''P. macromerus'' was based on this trait, a suggested similar symphyseal tooth count (six) between OUMNH J.10454 and the proposed neotype of ''P. macromerus'', and their occurrence at approximately the same stratigraphic level. However, a reexamination of NHMUK PV OR 39362 (proposed neotype of ''P. macromerus'') by Benson ''et al.'' (2013), revealed that it had at least seven symphyseal tooth, but more likely nine. Therefore, they considered ''P. rossicus'' to be a valid species of ''Pliosaurus'' based on the presence of an autapomorphic short symphysis containing only six alveoli, and tentatively referred OUMNH J.10454 (and thus possibly OUMNH J.50376 and OUMNH J.50377) to ''P. ? rossicus''. Another possible difference between NHMUK PV OR 39362 and OUMNH J.10454, is that the latter had greater mandibular tooth count of approximately 60, although this is possibly an artifact of its reconstruction according to Knutsen (2012).

''Pliosaurus irgisensis''

''P. irgisensis'' was first described and named by Nestor Ivanovich Novozhilov in 1948, under the name ''Peloneustes irgisensis''. The specific name is derived from the name of the Maly Irgiz River, where the holotype was found. The holotype, PIN 426 housed at Paleontological Institute, Russian Academy of Sciences, consists of partial cranium and postcranium of a medium-sized individual. The cranial remains of PIN 426 are currently suffering from the effects of pyrite decay, and its associated remains have been lost. It was collected at Savel-evsk Mine No. 1, of eastern Saratov Oblast, European part of Russia, from the middle Volgian stage (also known as middle Tithonian). Novozhilov (1964) reassigned the material to a new genus, ''Strongylokrotaphus'', meaning "round" (''strongylos'') "temple" or "head" (''krotaphos'') in Ancient Greek. These assignments were criticized by other workers, including Tarlo (1960), Halstead (1971) and Storrs ''et al.'' (2000), because of the general and non-specific diagnosis for ''Strongylokrotaphus'', and differences from the type species of ''Peloneustes''. ''P. irgisensis'' might be synonymous with ''P. rossicus'' based on their similar sizes and stratigraphic co-occurrence, as the only difference between the species is ontogenetic. Knutsen (2012) considered the material to be non-diagnostic and referred ''P. irgisensis'' to Pliosauridae indet, as dentition, which is autapomorphic in ''Pliosaurus'', was not described from PIN 426. Benson ''et al.'' (2013) also considered this species to be a '' nomen dubium'', referring it to Thalassophonea indet, and stating that PIN 426 requires re-description.

''Pliosaurus portentificus''

''Pliosaurus portentificus'' is known from the late Kimmeridgian of England. Considered by Knutsen (2012) and Benson ''et al.'' (2013) to be undiagnostic, with its holotype specimen most likely being a juvenile individual of one of the other species of ''Pliosaurus''.

Description

Using '' Liopleurodon'', another large pliosaurid, as a guide, a specimen found in the Svalbard islands of northern Europe has been estimated to have been long, in body mass and had teeth long. It is estimated to have lived approximately 147 million years ago."Fossil 'makes T-Rex look feeble'"
, news24.com, 17 March 2009. Later on, thorough scrutiny of this Svalbard specimen revealed that it was not as massive as originally claimed; total length estimates have been revised to and was named ''Pliosaurus funkei'' in Knutsen et al. (2012), with estimated skull lengths of and a forelimb length of for the holotype (PMO 214.135), and an estimated skull length of for the referred specimen (PMO 214.136), suggesting that the animal had proportionally bigger flippers than other pliosaurs compared to the skull size and dimensions of the vertebrae. Gregory S. Paul proposed that most species reached in length and in body mass, while ''P. rossicus'' reached in length and in body mass; he also agreed with the estimate of ''P. funkei'' by Knutsen et al. (2012) and noted that the largest known examples may have exceeded and weighed up to . Analysis of bones from the four flippers suggest that the animal cruised using just two fore-flippers, using the back pair for extra speed when pursuing and capturing prey. ''P. funkei'' brain was of a similar type and size, proportionally, to that of today's great white shark.

Phylogeny

The cladogram below follows a 2013 analysis by paleontologists Benson ''et al''.

See also

* Timeline of plesiosaur research

References

External links

*
* https://www.reuters.com/article/scienceNews/idUSL2771508220080227?pageNumber=2&virtualBrandChannel=0

Gigantic Pliosaurus discovered on Norwegian soil



Sea Monsters: A Prehistoric Adventure Movie - Interactive Time Line - National Geographic

Britannica Online Encyclopedia

BBC Earth (video): The most powerful marine reptile ever

{{Taxonbar, from=Q134771

Pliosaurids
Kimmeridgian life
Tithonian life
Late Jurassic plesiosaurs of Europe
Jurassic England
Fossils of England
Jurassic Norway
Fossils of Svalbard
Agardhfjellet Formation
Jurassic Russia
Fossils of Russia
Fossil taxa described in 1842
Taxa named by Richard Owen
Sauropterygian genera