User:Macrophyseter/sandbox
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| Mounted reconstruction of the T. proriger "Bunker" specimen (KUVP 5033) at the Rocky Mountain Dinosaur Resource Center | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Reptilia |
| Order: | Squamata |
| Clade: | †Mosasauria |
| Superfamily: | †Mosasauroidea |
| Family: | †Mosasauridae |
| Clade: | †Russellosaurina |
| Subfamily: | †Tylosaurinae |
| Genus: | †Tylosaurus Marsh, 1872 |
| Type species | |
| †Tylosaurus proriger Cope, 1869
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| Species | |
Disputed or unpublished
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| Synonyms | |
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List of synonyms
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Tylosaurus (/ˌtaɪˈloʊˈsɔːrəs/; "knob lizard"[a]) is a genus of russellosaurine mosasaur (an extinct group of predatory marine lizards) that lived about 92 to 66 million years ago during the Turonian to Maastrichtian stages of the Late Cretaceous. It fossils have been found primarily around North Atlantic Ocean including in North America, Europe, and Africa. The earliest discoveries were possibly made by Native American tribes in the Great Plains (submerged under a vast inland sea during the Cretaceous), whose creation myths spoke of giant serpentine water monsters turned to stone in ancient times. Paleontologist Edward Drinker Cope first scientifically described fossils of the genus from Kansas in 1869, but the name Tylosaurus was coined by Cope's rival Othniel Charles Marsh.
With a geologic span of over 25 million years, Tylosaurus was one of the most successful mosasaur genera in terms of diversity and longevity. It was both among the first and last of the group and had diversified into at least 8 valid species. The earliest representative, T. nepaeolicus, had already developed a large body size reaching 6 meters (20 ft) by its first appearance during the mid-Turonian. Its subsequent evolution into T. proriger through peramorphosis is well-documented in the fossil record. The lineage progressively grew in body size until T. proriger achieved a maximum length of at least 14 meters (46 ft) by the mid-Campanian, making it one of the largest mosasaurs. Other species were similarly large with documented top lengths varying between 8–12 meters (26–39 ft).
Description[edit]
Size[edit]
Tylosaurus was one of the largest known mosasaurs. The largest well-known specimen, a skeleton of T. proriger from the University of Kansas Natural History Museum nicknamed "Bunker" (KUVP 5033), has been estimated to measure between 12–15.8 meters (39–52 ft) long.[8][9] A fragmentary skeleton of another T. proriger from the Sternberg Museum of Natural History (FHSM VP-2496) may have been even larger; Everhart estimated the specimen to come from a 14 meters (46 ft) individual[10] compared to his 12 meters (39 ft) estimate for Bunker.[11] The genus exhibits Cope's rule, in which its body size has been observed to generally increase over geologic time.[8] In North America, the earliest representatives of Tylosaurus during the Turonian[12] and Coniacian (90-86 mya), which included early T. nepaeolicus and its precursors, typically measured 5–7 meters (16–23 ft) long[8] and weighed between 200–500 kilograms (440–1,100 lb).[13] During the Santonian (86-83 mya), T. nepaeolicus and newly-appearing T. proriger were 8–9 meters (26–30 ft) long[8] and weighed around 1,100 kilograms (2,400 lb).[14] By the Early Campanian, T. proriger attained lengths of 13–14 meters (43–46 ft).[15] Everhart speculated that because mosasaurs continuously grew throughout their lifetime, it would have been possible for some extremely old Tylosaurus individuals to reach 20 meters (66 ft) in absolute maximum length. However, he stressed the lack of fossil evidence suggesting such sizes and the odds against any being preserved.[16]
Other Campanian-Maastrichtian species were similarly large. The most recent maximum estimate for T. bernardi is 12.2 meters (40 ft) by Lindgren (2005); historically the species was erroneously estimated at even larger sizes of 15–17 meters (49–56 ft).[17] A reconstruction of T. saskatchwanensis by the Royal Saskatchewan Museum estimated a total length of over 9.75 meters (32.0 ft).[18] A mounted skeleton of T. pembinensis nicknamed "Bruce" at the Canadian Fossil Discovery Centre measures at 13.05 meters (42.8 ft) long and was awarded a Guinness World Records for "Largest mosasaur on display" in 2014.[19] However, the skeleton was assembled for display prior[20] to Bullard and Caldwell (2010)'s reassessment that found the species' number of vertebrae to be exaggerated.[21] T. 'borealis' is estimated at 6.5–8 meters (21–26 ft) in total length.[22]
Skull[edit]
The largest measured skull of Tylosaurus is Bunker's, estimated at 1.7 meters (5.6 ft) long.[23] Depending on age and individual variation,[23] it made up between 13-14% of the total skeleton length.[24] The head was strongly conical and the snout proportionally longer than many mosasaurs with exceptions like Ectenosaurus.[25]
Jaws and teeth[edit]
The upper jawbones are comprised of the premaxilla and maxilla, while the sole tooth-bearing lower jawbone is the dentary. Together, their teeth forms the marginal dentition. The jaws were elongate; the dentary is between 56-60% of total length of the entire lower jaw in adult T. nepaeolicus and T. proriger,[23] about 55% in T. pembinensis,[26] and 62% in T. saskatchwanensis.[27] It is about 55% of the total skull length, which is slightly shorter than the lower jaw, in T. bernardi.[17] The dentary is robust and strong, though not as strongly built as Mosasaurus, Prognathodon, or Plesiotylosaurus.[28] The jawline ranges from flat[5] to slightly concave.[21][29] A small dorsal ridge appears right ahead of the frontmost dentary tooth in at least mature individuals of T. nepaeolicus and T. proriger.[23] The maxilla in at least T. bernardi is long and slender.[30] Like all mosasaurs, Tylosaurus also had teeth in the pterygoid bone, the rear bone of the palate.[31] The pterygoid teeth probably functioned to perform ratchet feeding, in which the teeth holds prey in place as the mosasaur's lower jaw slides back and forth in a streoptostylic manner enabled through a modified jaw joint.[32] In each half of the skull, Tylosaurus had 2 premaxillary teeth and 12 to 13 maxillary teeth in the upper jaw, 13 dentary teeth on the lower jaw, [5] and 10 to 11 pterygoid teeth (possibly more in juveniles).[b][23][5] The genus displayed a mostly homodont dentition, meaning that its teeth were minimally different in size and shape.[33][21][2] Only the pterygoid teeth significantly differed from the rest.[34]
The marginal dentition of most species is adapted for cutting large marine vertebrates,[22][35] while those in T. ivoensis and T. gaudryi appear more optimized for piercing or smashing prey.[4] Marginal teeth are triangular with a slight recurve towards the back of the jaws so that the lingual (tongue-facing) side forms a U-shaped curve.[33] From top view, they are compressed at the lingual and labial (front lip facing) sides to form an oval-like shape.[36][37] Teeth of immature T. proriger are initially compressed, but become conical in adulthood.[34][38][39] Compression were initially believed to occur at the lingual and buccal (side tongue facing) sides in T. bernardi,[34] but the latest examination by Jiménez-Huidobro and Caldwell (2016) found its teeth be be labiolingually compressed. Cutting edges are finely serrated with small denticles[5][30][36] except in juvenile T. nepaeolicus.[36] In T. pembinensis, they are faint.[21] The teeth generally hold a pair of cutting edges facing the front and back of the jaws, but some front teeth may have only one on the front side.[36][27] The placement of cutting edges if paired are not always equal; in at least T. proriger, T. ivoensis, T. gaudryi,[34] and T. pembinensis, they are positioned such that the surface area of the tooth's lingual side is greater than the buccal.[21] Both sides are always balanced in area in T. bernardi.[34] The enamel surface is lined with thin fine ridges called striations that run vertically from the tooth's base. Surface is also either smooth or faintly faceted, in which it is flattened into multiple sides to form a prism-like geometry.[4]
Bardet et al. (2006) classified Tylosaurus species into two morphological groups based on marginal dentition. The North American 'proriger group' includes T. proriger and T. nepaeolicus and is characterized by teeth with smooth or faint facets, less prominent cutting edges, and a vein-like network of primitive striations extending to near the tip.[40] The group was originally defined as having slender teeth,[40] but subsequent research has since recognized that slenderness is an ontogenetic trait in T. proriger with robust teeth appearing in adult forms.[39] Though not formally classified within a group, the marginal teeth of T. saskatchwanensis shares a comparable morphology with T. proriger.[27] The second is the Euro-American 'ivoensis group' and consists of T. ivoensis, T. gaudryi, and T. pembinensis. Their teeth are robust with prominent cutting edges with striations on the lingual and occasionally buccal sides that do not reach the tooth's tip, and facets on the buccal side.[40] The facets are gentle in T. pembinensis,[21] while in T. ivoensis they are slightly concave.[34] The latter feature is also known as fluting.[41] Marginal teeth in T. gaudryi are virtually indistinguishable from those in T. ivoensis.[34] T. iembeensis was not placed within either group; no further description is known of its teeth other than having striations and no facets.[40] The distinction of an 'ivoensis group' is contentious. Caldwell et al. (2008) argued that T. pembinensis cannot be compared with T. ivoensis as the former's teeth are not fluted, and that T. ivoensis is more allied with the distinctively fluted teeth of Taniwhasaurus.[41] Jiménez-Huidobro and Caldwell (2019) listed the absence of marginal fluting as an genus-identifying trait that differentiates Tylosaurus from Taniwhasaurus.[5]
Pterygoid teeth are smaller and more recurved than marginal teeth.[31] The base of the former are nearly circular but divided into a front and back-facing side of near-equal surface area via a pair of faint buccal and lingual cutting edges. This is except in T. gaudryi, where the teeth are compressed at the lingual and labial sides and hold distinct cutting edges at the front and back sides.[34] Cutting edges are not serrated in all named species where it is known.[30][4] Past studies claimed to have identified serrations in T. bernardi, but the latest examination by Jiménez-Huidobro and Caldwell (2016) found none.[30] The typical front-facing side is either smooth of faintly faceted, while the back-facing side is striated. Tooth build is robust in at least T. ivoensis.[34]
Cranium[edit]
The most recognizable characteristic of Tylosaurus is the elongated conical rostrum that protrudes from its snout, from which the genus is named after. This is formed by the elongation of the front end of the premaxilla[29] and dentary.[27] Unlike typical mosasaurs, Tylosaurus did not have teeth up to the end of the snout nor on the bony prow that is the rostrum. This feature is not present at birth but rapidly developed during infancy[42] and is believed to have been primarily used for combat purposes such as ramming.[43][29][42] Once developed, the rostrum starts as an acutely-angled rounded shape in immature T. nepaeolicus and T. proriger, but takes on a broader rectangular form in mature individuals[42][23] and in T. saskatchewanensis,[27] T. bernardi,[30] and T. pembinensis.[21] The prow is supported by a broad and robust internarial bar (the extension of the premaxilla on top of the skull that held together the nasal and upper jaws), which provided effective shock absorption and stress transfer following a frontward collision.[29] Additional protective adaptations include a robust braincase that forms a sliding joint with the roof of the back of the skull, cushioning the brain from blunt-force trauma,[29] and in later species,[c][21][30][27] an interlocking suture between the rostral portion of the premaxilla and front end of the maxilla to form a sinusoidal shape resembling a pair of buttresses, which acted as a reinforced strut.[29] The prow holds the terminal branches for the trigeminal nerves through randomly scattered foramina.[44] Exits are also lined along the maxilla right above the gum lines.[45]
The external nares, or body nostril openings, are another important diagnostic character. The premaxilla, maxilla, and frontal bones form its rims; unlike typical mosasaurs the prefrontal bones are not involved.[5] The nares open somewhere above the fourth maxillary tooth from the front end and extends until it touches the frontal; in T. proriger it opens directly above or slightly behind the tooth[d], while in T. nepaeolicus it begins between the third and fourth maxillary teeth,[21] T. bernardi towards the end of the fourth tooth,[30] and T. pembinensis right above the same tooth.[21] Nare length relative to the skull varied between species. It is proportionally short in T. proriger at 20-26% of total skull length,[47][34] T. bernardi at around 24%,[21] and T. gaudryi at 25-27%,[34] while long in T. pembinensis at 28-31%.[21] The nasal bones occupied the back half of the external nares. They were either free-floating or lightly articulated to the internarial bar light sutures at the front ends.[29] The back ends reached close proximity to the frontal but not full contact.[47] The nasals' loose association with the rest of the skull may be why the bones are frequently lost and therefore exceedingly rare;[47] it is known in only two skulls of T. bernardi and T. sp. They came in free pairs that were independent of each other; this is unlike in living monitor lizards where the nasals are fused into one unit. Tylosaurus is the only mosasaur where free nasal pairs are clearly documented.[29] The only record of nasals in other mosasaurs[e][29] is in the holotype of Plotosaurus, where one is missing,[50] so it unclear whether the paired trait is a plesiomorphy of just the tylosaurines or of mosasaurs broadly.[29] The external nares lead to the choanae (internal nares) at the bottom of the cranium, which provides passage from the nostrils to the throat.[51] In Tylosaurus, they are shaped like a compressed teardrop. The choanae are constrained in extent by the vomers and palatine bone to the back half of the maxilla.[52] Ahead of the choanae, each vomer holds a small groove that held the Jacobson's organ, which is involved in the tongue-based sense of smell. It begins opposite of the fourth maxillary tooth in Tylosaurus,[53] and also ends immediately past the fifth maxillary tooth in T. bernardi.[29] The exit point for the veins leading to sinuses inside the palatine occur right in front of the Jacobson's organ between the vomers and maxilla. This differs from living monitors, where the exit occurs behind the organ.[52]
The frontal bone usually possesses a small sagittal crest along its midline. It is most prominent in T. proriger.[5][36] It is moderately developed in T. saskatchewanensis[27] and T. bernardi, and also extends into the premaxilla for the latter.[30] The frontal crest is present but poorly developed in most T. nepaeolicus skulls, and occasionally lost in some mature individuals.[23] The frontal overlaps parts of the prefrontals that do not form the orbits (eye sockets), and at its rear end, articulates with the parietal bone through a frontoparietal suture. The shape of the suture is plastic[5] and can be anywhere between straight to strongly M-shaped, which in at least T. nepaeolicus and T. proriger appear to be ontogenetic variations.[23] The position of the pineal eye on the parietal is likewise variable, either appearing close to the frontoparietal suture or directly overlapping with it.[30][36] The orbits are formed by the prefrontal, postorbitofrontal, and jugal bones. The prefrontals and postorbitofrontals overlap at the top of the orbits, preventing the frontal bone from contributing to the sockets' shape.[5] The jugal forms the bottom of the orbit; in Tylosaurus, it is L-shaped and has a distinctive serif-like extension at the lower back corner of the junction between the horizontal and vertical rami (arms) called the ventroposterior process.[f][36] The vertical ramus is overlapped by the postorbitofrontal in most species[27][21][36], and horizontal ramus by the maxilla in T. pembinensis.[21] In H. bernardi, the vertical ramus is not overlapped but joins with the postorbitofrontal by a suture, and is diagnostically much thicker than the horizontal ramus.[30]
The quadrate bones are located at the back corners of the skull. They served as joints connecting the lower jaw to the cranium,[54] and carried the eardrum.[55] Several parts of the bone capture distinctive homologous variations[56] considered diagnostic up to the species level; some species can be differentiated based on the quadrate.[5] Ecology appears to be a key driver of quadrate morphology in squamates, and as a result may be a major factor for its variation between Tylosaurus species.[56] On the side facing away from median plane of the skull, the quadrate initially resembles a hook in immature T. nepaeolicus and T. proriger individuals, but in adult forms for both species[23] and in T. bernardi,[5][30] T. pembinensis,[21] and T. saskatchweanensis it takes on a robust oval-like shape.[27] The main body, known as the shaft, holds a broad concavity called the tympanic conch that takes up most of its extent in this view, which held the eardrum.[55] It is shallow in T. nepaeolicus,[56] T. proriger, and T. bernardi,[5] while deep and bowl-shaped in T. pembinensis[56] and T. saskatchewanensis.[5] The rim of the conch closer to the front of the skull, called the tympanic ala, held the attachment points to several jaw-closing muscles.[57] It is thin in T. nepaeolicus, T. proriger,[23] and T. bernardi,[30] also wide and flat in the former two,[23] thicker than T. bernardi in T. pembinensis,[30] and thick in T. saskatchewanensis.[27] Emerging from the top of the shaft is the suprastapedial process, which curves towards the backward direction of the skull into an incomplete loop and served as the attachment point for the depressor mandibulae muscles that open the lower jaw[21][57] through prominent insertion grooves on the top and side surfaces.[56] It is slender and proportionally long in immature T. nepaeolicus and T. proriger, giving their quadrates the hook-like appearance, but by adulthood is thick and reaches about half the length of the entire bone.[58] The process is of similar relative length in T. saskatchwanensis[27] but probably shorter in T. bernardi.[30] In T. pembinensis, it abruptly turns inward to face the skull's median plane at a 45° downward angle and therefore difficult to measure.[21] Emerging from the lower back-facing rim of the quadrate is the infrastapedial process. Its shape changes during maturity in T. nepaeolicus and T. proriger. For the former, the process is absent in juveniles but appears as a small development in adults, while it is already present as a subtle point in juveniles and becomes a distinctively broad semicircle in adults for the latter.[23] It was probably poorly developed in T. bernardi.[30] In T. pembinensis[21] and T. saskatchewanensis,[27] the infrastapedial process is rounded and located high on the lower half of the rim; for the latter species the suprastapedial process almost touches it.[27] At the bottom of the shaft is the mandibular condyle, which is the joint connected to the lower jaw. It is rounded in all adult species where known,[56][59][27][23] but initially does not exist in infant T. nepaeolicus and T. proriger.[23] On the side facing towards the skull's median plane in at least T. nepaeolicus and T. pembinensis, there is a thick vertical ridge that lines the shaft's surface, which protrudes at the top of the quadrate like a pillar.[56]
Braincase[edit]
Postcranial skeleton[edit]
Vertebrae and ribcage[edit]
Like all mosasaurs, the vertebral column of Tylosaurus is divided into 5 parts. The frontmost section is the cervical vertebrae, which forms the neck. The first cervical, the atlas, articulates with the occipital bone of the braincase and is unique in shape. A pair of neural arches appear from opposite sides of the median plane the central body (centrum), or odontoid,[g], which turn downwards to connect with a bone called the intercentrum located below the odontoid. They together form a ring-like structure. None of these bones are fused together. The spinous processes of the neural arches raise above the odontoid and are short for a mosasaur.[61] They curve towards the middle to almost touch each other in T. nepaeolicus,[36] while they remain widely separated in T. proriger,[62] T. bernardi,[59] and T. saskatchewanensis.[27] Distinct extensions from the outward sides of the neural arches, the lateral processes, are rectangular-like in at least T. bernardi[59] and T. saskatchewanensis.[27] The synapophysis, which also emerge from each arch's outward side to point backwards and is related to the level of development of the cervical iliocostalis muscles, is either large or almost nonexistent.[62] The second cervical is also known as the axis. It is a robust vertebra[63] with a circular centrum in at least T. saskatchewanensis[27] that served as the source of many skull muscles.[63] The neural arches are fused to the centrum and with each other to form a single arch and neural spine; in T. nepaeolicus there is still a visible suture between the two arches.[36] The neural spine is wide and flat at the sides. A pair of transverse processes, which served as attachment points for muscles and ligaments involved in spinal movement, extends horizontally outwards from the sides of the centrum in a short and wide shape.[36][27] Emerging from the bottom surface of the centrum is the hypapophysis, which extends backwards to contact with the cervical behind the axis.[64]. It is rounded in T. nepaeolicus,[36] T. bernardi,[30] and T. saskatchewanensis[27] while conical in T. pembinensis.[21] A single pair of zygopophyses, which emerge from the neural arch towards the back, also extend backwards at about a 45° angle to interlock with the vertebra.[63] The remaining cervicals are similar with each other in structure. The centrum is horizontally oval-like and wider than tall when viewed towards the coronal plane.[21][59][36][27] In T. pembinensis, the length-width ratio is approximately 1.25:1.[21] The hypapophysis and transverse processes are present, but the latter is directed upwards.[21][59][36][27] Two pairs of zygopophyses are present at the front and back corners of the neural arch. The front pair projects at a diagonally upward, forward, and outward direction to connect with the vertebra before it. It is supported by a rounded crest from the synapophysis that is straight in Tylosaurus. The back pair projects diagonally downward, backward, and upward.[65] Unlike some mosasaurs, the zygosphene and zygantrum are absent.[65][21][59][27] The shape of the neural spines slowly changes so that by the last cervical it is shaped like a flat parallelogram pointed backwards in side view.[66] Articulated to the surface of the transverse processes[59][36][27] are short ribs that do not form a rib cage. Ribs are present in all cervicals except the atlas.[67] There are 7 cervicals in total; the number appears to be universal in mosasaurs,[68] so it is often presumed that Tylosaurus species have it even if fossil documentation is incomplete.[h][21][27]
The dorsal vertebrae are the next series and form the thorax and lumbar. The first dorsal is distinguished by the articulation of its ribs to the pectoral girdles; the front dorsals are otherwise identical to the last cervical. The dorsal series extends all the way to the pelvic region. The last dorsal occurs right ahead of the rear limbs. The vertebrae gradually changes in morphology as it progresses.
from neck to tail into cervical (neck), dorsal (thorax and lumbar), pygal (pre-chevron tail), and caudal (chevron-bearing tail) vertebrae. Caudal vertebrae is further subdivided into intermediates, which have transverse processes that served as attachment points for tail muscles and ligaments, and terminals which lack them. The transition from cervical to dorsal vertebrae is marked by the articulation of the ribs to the pectoral girdle. Mosasaurs appear to universally have 7 cervicals, so it is often presumed that all species have such number even if the ribs are not preserved.[i] Dorsal and pygal vertebrae are separated by the appearance (but not articulation) of the pelvis between them in side view. A complete vertebral series is documented only in T. proriger. Its column is composed of 7 cervicals, 22-23 dorsals, 6-7 pygals, 33-34 intermediate caudals, and 56-58 terminal caudals. The pre-caudal series is also well known in several other species and greater in count than the type species. T. bernardi has 26 dorsals and 7 pygals, while T. pembinensis has 29 dorsals but an unknown number of pygals. T. saskatchewanensis is the most elongate, with 39 dorsals and 9 or 10 pygals.
Thorax[edit]
Limbs and girdles[edit]
Flippers no longer represent active locomotors but just stabilizers (saskatchewanensis paper)
Soft tissue[edit]
Skin and coloration[edit]
Fossil evidence of the skin of Tylosaurus in the form of scales has been described since the late 1870s. These scales were small and diamond-shaped and were arranged in oblique rows, comparable to that found in modern rattlesnakes and other related reptiles. However, the scales in the mosasaur were much smaller in proportion to the whole body.[69][70] An individual measuring 5 meters (16 ft) in total body length had dermal scales measuring 3.3 by 2.5 millimeters (0.130 in × 0.098 in),[71] and in each square inch (2.54 cm) of the mosasaur's underside an average of ninety scales were present.[69] Each scale was keeled in a form resembling that of a shark's denticles.[70] This probably helped reduce underwater drag[70] and reflection on the skin.[72]
Microscopic analysis of scales in a T. nepaeolicus specimen by Lindgren et al. (2014) detected high traces of the pigment eumelanin indicative of a dark coloration similar to the leatherback sea turtle in life. This may have been complemented with countershading, present in many aquatic animals, though the distribution of dark and light pigments in the species remains unknown. A dark-colored form would have provided several evolutionary advantages. Dark coloration increases absorption of heat, allowing the animal to maintain elevated body temperatures in colder environments. Possession of this trait during infancy would in turn facilitate fast growth rates. Unreflective dark coloring and countershading would have provided the mosasaur with increased camouflage. Additional speculative functions includes increased tolerance to solar ultraviolet radiation, strengthened integuments. The study remarked that certain melanism-coding genes are pleiotropic for increased aggression.[72]
Respiratory system[edit]
AMNH FR 221 preserves parts of the cartilaginous respiratory system. This includes parts of the larynx (voice box), trachea (windpipe), and bronchi (lung airways). They were however only briefly described in the preserved position by Osborn (1899). The larynx is poorly preserved; a piece of its cartilage first appears below just between the pterygoid and quadrate and extends to behind the latter. This connects to the trachea, which appears below the atlas vertebra but is not preserved afterwards. The respiratory tract reappears below the fifth rib as a pair of bronchi and extends to just behind the as-preserved coracoids where preservation is lost.[73] The pairing is suggestive of two functional lungs like modern limbed lizards but unlike snakes.[74] Similar branching is also found in Platecarpus[74] and putatively Mosasaurus, the only two other derived mosasaurs with their respiratory systems documented.[75] The bifurcation point for the Tylosaurus specimen is anywhere between the first and sixth cervical vertebrae.[j][73] In Platecarpus, the bronchi probably diverged below the sixth cervical into near-parallel pairs,[76] while in Mosasaurus the organ is dislocated.[75] A bifurcation point's position ahead of the forelimbs would be unlike terrestrial lizards, whose point is within the chest region, but similar to the short trachea and parallel bronchi of whales.[74]
History of study[edit]
Discovery and naming[edit]
Tylosaurus was the third new genus of mosasaur to be described from North America behind Clidastes and Platecarpus and the first in Kansas.[77] The early history of the genus as a taxon was subject to complications spurred by the infamous rivalry between American paleontologists Edward Drinker Cope and Othniel Charles Marsh during the Bone Wars.[77][78] The type specimen was described by Cope in 1869 based on a fragmentary skull measuring nearly 5 feet (1.5 m) in length and thirteen vertebrae lent to him by Louis Agassiz of the Harvard Museum of Comparative Zoology.[79] The fossil, which remains in the same museum under the catalog number MCZ 4374, was recovered from a deposit of the Niobrara Formation located in the vicinity of Monument Rocks[80] near the Union Pacific Railroad at Fort Hays, Kansas.[81] Cope's first publication of the fossil was very brief and was named Macrosaurus proriger, the genus being a preexisting European mosasaur taxon.[77][79] The specific epithet proriger means "prow-bearing", which is in reference to the specimen's unique prow-like elongated rostrum[82][78] and is derived from the Latin word prōra (prow) and suffix -gero (I bear).[83] In 1870, Cope published a more thorough description of MCZ 4374. Without explanation, he moved the species into another European genus Liodon and declared his original Macrosaurus proriger a synonym.[77][81]
In 1871, Cope identified a second species of North American Liodon based on several vertebrae and limb fragments, which he named Liodon dyspelor. The fossils came to Cope under the label as having been collected by an army doctor named William B. Lyon at Fort McRae, New Mexico.[84][85] However, a 1997 study led by David C. Parris of the New Jersey State Museum found that the chemical composition of the fossil did not match any known geological deposit in New Mexico and is instead identical to that of the Niobrara Formation; the study speculated from examinations of multiple letters between Lyon and the Smithsonian Institution that the Liodon dyspelor fossils were actually recovered from somewhere in Western Kansas and were mislabeled as being collected by Lyon in New Mexico (who was shipping a different fossil from Fort McRae around the same time) during transit. The type specimen of the taxon is split between two museums; some of the vertebrae went to Cope's American Museum of Natural History as AMNH 1580 while the rest were sent to the Smithsonian as USNM 41.[85]
In 1872, Marsh argued that Liodon proriger and Liodon dyspelor are taxonomically distinct from the European genus and must be assigned a new one. For this, he erected the genus Rhinosaurus, which means "nose lizard" and is a portmanteau derived from the Ancient Greek words ῥίς (rhī́s, meaning "nose") and σαῦρος (saûros, meaning "lizard"). Marsh also described a third species based on a partial skeleton he collected near the southern portion of the Smoky Hill River[86] that is now in the Yale Peabody Museum as YPM 1268,[87][88] which Marsh named Rhinosaurus micromus.[86][88] Cope responded by arguing that Rhinosaurus was already a preoccupied synonym of Liodon. He disagreed with Marsh's arguments but proposed that in case Marsh was indeed correct, the genus name Rhamphosaurus should be used.[89] Marsh later discovered that the taxon Rhamphosaurus was preoccupied as a genus of lizard named in 1843. As a result, he suggested a move to a newly erected genus named Tylosaurus.[90] This name means "knob lizard" in another reference to the elongated rostrum characteristic of the genus. It is derived from the Latin tylos (knob) and Ancient Greek σαῦρος.[78] Despite coining the new genus, Marsh never formally transfered the Rhinosaurus species to Tylosaurus; this was first done in 1873 by Joseph Leidy of the University of Pennsylvania by transferring Rhinosaurus proriger and Rhinosaurus dyspelor to Tylosaurus.[8][91] Rhinosaurus micromus was formally transferred to the same genus in 1894 by John Campbell Merriam, a paleontologist of the University of Munich at the time.[92]
Tylosaurus subsequently became the near-universally accepted genus for T. proriger, T. dyspelor, and T. micromus. An exception to this adoption was Cope,[89] who refused to accept Marsh's new genus and continued to refer to its species as Liodon. Cope also insisted that Rhamphosaurus was not preoccupied, arguing that while it was indeed used as a genus of lizard, it was subsequently synonymized with other genera before 1872 and was thus a vacant taxon.[82] Cope's persistence can be seen in his 1874 description of the fourth described species of Tylosaurus, which he named Liodon nepaeolicus. This type specimen of this species consists of a right lower jaw, a partial upper jaw, a quadrate bone, and a dorsal vertebra and was discovered by geologist Benjamin Franklin Mudge in an unspecified deposit of Cretaceous grey shale about a half-mile south of the Solomon River. The fossils are stored in the American Museum of Natural History under the catalog number AMNH 1565. The specific epithet nepaeolicus is in reference to the Nepaholla, the Native American name for the Solomon River.[8] Liodon nepaeolicus was formally transferred to the genus Tylosaurus in Merriam's 1894 publication.[92]
19th and 20th century developments[edit]
Early depictions[edit]
The earliest depictions of Tylosaurus can be traced back to Cope's 1870 description of MCZ 4374. He suggested that Tylosaurus was an "excessively elongate reptile" because four of the back tail vertebrae of the specimen were less than a fifth in diameter than one more proximal, or closer to, the base of the tail, and there was little dimensional variation between the four back tail vertebrae. To Cope, this indicated that the enormous decrease in the size of the tail vertebrae from the base to the tip of the tail was minimal between vertebrae; thus, in order for the vertebrae in the column to approach the size of the tail vertebrae based on the observed rate of size decrease per vertebrae, plentiful amounts of vertebrae would have been needed. By measuring the proportions of the change in dimensions between the vertebrae, Cope estimated that Tylosaurus had at minimum over sixty vertebrae between the described proximal tail vertebra and a hypothetical vertebra measuring half the diameter of the four back tail vertebrae. Cope speculated that there were even more tail vertebrae ahead of the proximal vertebra, justified by the small transverse process it possessed, which would increase the vertebral count in the tail to an unknown but monstrous amount.[81] The resulting animal became that akin to an enormous sea serpent-like reptile reaching lengths rivaling that of the largest whales.[93][94][95] In an 1872 publication, Cope described in detail his imagination of the appearance of Tylosaurus. He depicted the head as akin to a giant flat cone supporting eyes directed partially upwards that is capable of swallowing entire prey whole like a snake, with a loose and baggy pelican-like throat to allow entry of such prey. Like a whale, one pair of paddle-like flippers was described to be present in the animal[93] and functional hind limbs were thought to be absent.[96][93] The tail was imagined as long and flat, propelling Tylosaurus forward via an anguilliform locomotion. Cope estimated that T. proriger measured at minimum 50 feet (15 m) in length. T. dyspelor was the largest species of the genus was also described as the longest of all reptiles. Its maximum length was estimated to equal that of the blue whale,[k][93] which reaches lengths of up to nearly 30 meters (98 ft) or more.[99] One T. dyspelor specimen with fossils relatively smaller than that of the taxon's type specimen had a skull measuring about 5 feet (1.5 m) in length; the whole animal was estimated to measure 75 feet (23 m) in total length.[93] In 1874, Cope estimated that T. nepaeolicus was around one-third the length of T. proriger,[8] which would translate to around 5.08 meters (16.7 ft) when using his 1872 estimates.[8][93]
One of the earliest restorations of Tylosaurus comes from an illustration by a popular artist named Henry Worrall for paleontologist William E. Webb's 1872 fictional book Buffalo Land. This illustration, which is titled The sea which once covered the plains, represents one of the first paleoart of marine reptiles and pterosaurs from the Niobrara Formation. At the center of the illustration rises a giant Tylosaurus (identified as Liodon proriger). The appearance of this mosasaur was influenced by Cope, who was an acquaintance of Webb, as evidenced by its excessively elongated tail and serpentine appearance.[100] Additionally, the Tylosaurus was given a rather long neck. Although not as long as those of plesiosaurs like Elasmosaurus, this detail would influence subsequent depictions of Tylosaurus in art. An example of this can be seen in the famous fossil collector Charles Hazelius Sternberg's 1889 fictional narrative The Young Fossil Hunters: A True Story of Western Exploration and Adventure, which contains a scene where a giant Tylosaurus skeleton measuring 80 feet (24 m) in total length with a long and slender neck that is 20 feet (6.1 m) long is uncovered.[95]
Increased understanding and complete skeletons[edit]
Paleontologists began to understand Tylosaurus as scientists do today beginning with Samuel Wendell Williston's 1898 publication of a comprehensive study of the skeletal anatomy of Kansas mosasaurs, which among many things corrected many of the erroneous beliefs held by earlier paleontologists about Tylosaurus. A central component of the publication was a rigorous skeletal reconstruction of T. proriger,[101][102] which was drawn by paleoartist Sydney Prentice under Williston's instructions. This reconstruction was almost entirely informed by three specimens in the collections of the University of Kansas Natural History Museum, but they nevertheless provided enough material to represent nearly an entire skeleton.[102] These three specimens include one consisting of a posterior fragment of the skull and an "absolute complete series of vertebrae, connected from head to tip of tail" collected in an unspecified date by a fossil collector named Elias Putnam West (KUVP 1048); one containing a complete skull and cervical vertebrae collected in 1898 by fellow colleague Handel T. Martin (KUVP 28705); and one collected in 1877 by university chancellor Francis H. Snow that contains a near-complete set of front paddles along with some ribs, vertebrae, and shoulder girdles (KUVP 1075).[102][103] Various additional Tylosaurus specimens informed minor missing body parts such as the hind limbs. The resulting animal was correctly depicted as a four-flipper reptile with a short neck and a tail making up around half the body length.[102] Rather unrealistically, the vertebral column was drawn straight and lacking in structural curves that Tylosaurus would have possessed in life. Commentating on this issue, Everhart noted that Williston was already aware of the curvature of a mosasaur's spinal column and suggested that he had a straight spine drawn to save space on the plate the reconstruction was published on. Nevertheless, apart from the straight spine, Williston's century-old skeletal reconstruction of T. proriger is still considered accurate by modern standards, and adaptations of the skeleton remain in use by paleontologists and museum workers.[104] In his own interpretation of the available fossil evidence, Williston proposed that Tylosaurus grew no larger than 35 feet (11 m) in length and lived as a highly mobile predator "at the expense of strength" that was best adapted for preying on small fish and occasionally an "animal of their own kind." In a review of the taxonomy of the Tylosaurus genus, Williston (1898) expressed doubt regarding the validity of T. micromus and T. nepaeolicus and went as far as to suggest the latter species was merely a juvenile representative of T. proriger. He also remarked that there exist little anatomical differences between T. proriger and T. dyspelor; the only real distinction between the two species being in size.[102]
In 1899, Henry Fairfield Osborn described the first complete skeleton of Tylosaurus, a specimen measuring 8.83 meters (29.0 ft) long that resides in the American Museum of Natural History as AMNH FR 221. Discovered in Kansas by a local named W. O. Bourne and initially identified as T. dyspelor, the fossil has been considered remarkable in that it contained not only every bone apart from a few in the tail's tip, but also had exceptional preservation of the animal's soft tissue, including the larynx, trachea, bronchi, and cartilage in the throat, chest, and shoulders. This was due to calcification, a condition in a calcium-rich environment like the Kansas chalk that causes soft tissue to harden, allowing it to better fossilize.[73] The completeness of AMNH FR 221 allowed Osborn to accurately measure the proportions of each body part;[73] these ratios remain in use by modern paleontologists when extrapolating Tylosaurus fossils.[8][22] Osborn (1899) included a life impression of AMNH FR 221 by paleoartist Charles R. Knight.[73] The restoration carried a number of erroneous features, such as a baggy throat, bloated belly, and inaccurate paddles and dorsal fin.[105] But a seminal feature was the addition of a dorsal crest (known as a fringe) lining the mosasaur's back. This was based on another 1898 description of a mosasaur fossil by Williston that erroneously identified tracheal rings as remains of a dorsal fringe, which he corrected in 1902. Knight updated his Tylosaurus restorations with the dorsal fringes removed to reflect this correction. However, his original depiction of a fringe was picked up as a meme, and many subsequent illustrations of the mosasaur continued to portray this inaccuracy.[106]
Additional largely complete skeletons of T. proriger and T. dyspelor were uncovered from the Niobrara Formation between the 1900s to 1920s by Charles Sternberg and his son George, which were sold to museums in the United States and Germany.[107] A particular find was a T. proriger skeleton collected by C. Sternberg from Smoky Hill Chalk deposits in Logan County, Kansas in 1917, which contained digested remains of a plesiosaur within its ribcage. The specimen was sold the following year to the Smithsonian, and the mosasaur has been permanently displayed as USNM 8898.[108][109] The plesiosaur remains, despite their significance, were stashed as a separate specimen and promptly forgotten until their redescription by Everhart in 2004. This rediscovery formed the basis for the plot of the 2007 National Geographic film Sea Monsters: A Prehistoric Adventure.[109] George Sternberg attempted to sell another complete T. proriger skeleton he found to the Smithsonian 1926, but the museum was satisfied with his father's earlier specimen and declined the offer. This skeleton was ultimately transferred to the Sternberg Museum as FHSM VP-3.[110]
In his landmark 1967 work Systematics and Morphology of American Mosasaurs, Dale Russell performed a complete review and redescription of Tylosaurus. In a taxonomic examination, Russell found little justification for recognizing the validity of T. dyspelor and declared it a nomem vanum,[84] along with recognizing T. micromus as a junior synonym of T. proriger.[89] Many of the complete skeletons formerly assigned to the former taxon were reassigned to the type species.[87] T. nepaeolicus was affirmed as a distinct species.[111] Russell (1967) provided extensive diagnoses of Tylosaurus that are still used by scientists today, and Everhart remarked that the work "remains the single best reference regarding the skeletons of the various mosasaur genera" like Tylosaurus.[112]
Hainosaurus and additional species[edit]
By Russell (1967), the only recognized valid species of Tylosaurus were T. proriger and T. nepaeolicus. However, throughout the 19th and 20th centuries, numerous species of mosasaurs were described from around the world that are now recognized within the genus Tylosaurus. These additional species were identified as different genera during their times of discovery and it was not until the early 21st century when they were reclassified as Tylosaurus.[5]
In 1885, Louis Dollo described the genus Hainosaurus from a near-complete but poorly preserved skeleton excavated from a phosphate quarry in the Ciply Basin near the town of Mesvin, Belgium.[113][29] The fossil was initially discovered as eight vertebrae by a worker in the January of the same year, who sold them to the Royal Belgian Institute of Natural Sciences. Based on information about the circumstances and locality of the discovery given the museum, it was recognized that the rest of the skeleton may have remained intact. In February, excavations were made under the authorization of an industrialist named Leopold Bernard, who managed the quarry the fossil resided in. The rest of the skeleton was recovered after a month of excavating between 500–600 cubic meters (650–780 cu yd) of phosphate, although a section of the tail was found to have been destroyed by erosion from an overlying deposit. The skeleton went to the museum, which was subsequently studied by Dollo, who recognized that it belonged to a new type of mosasaur. By instruction of the museum, he named it Hainosaurus bernardi. The prefix Haino- in the generic name refers to the Haine, a river located nearby the Ciply Basin, and thus combined with σαῦρος means "lizard from the Haine"; Dollo wrote that this was erected specifically to complement the etymology of Mosasaurus, which was similarly named in reference to a river near its type locality. The specific epithet bernardi was in recognition of Bernard, who made the excavation of the skeleton possible.[113] The skeleton is now on display at the Royal Belgian Institute under the catalog number IRSNB R23.[29]
A second species historically pertained to Hainosaurus was described by in 1988 by Elizabeth Nicholls based on a partial skeleton consisting of a partial skull, lower jaw, a near-complete vertebral column, and some limb bones recovered from the Pembina Member of the Pierre Shale in Manitoba, Canada. This skeleton resides in the Miami Museum in Miami, Manitoba cataloged as MT 2. Although Hainosaurus was previously only known in Europe, Nicholls (1988) argued that the new species differed from the more locally known Tylosaurus based on a higher count of pygal vertebrae, longer external nares, and femur longer than the humerus. The species was named Hainosaurus pembinensis, the specific epithet referring to the Pembina Member the skeleton was found in.[26]
In 2005, paleontologist Johan Lindgren suspected that Hainosaurus pembinensis was actually a species of Tylosaurus but stated that a better description of MT 2 was needed to be certain.[17] In 2010, paleontologists Timon Bullard and Michael Caldwell redescribed such specimen. They argued that the pygal vertebrae reported by Nicholls (1988) actually belonged to another individual mosasaur, reducing the vertebral count in MT 2 to one that was indistinguishable with Tylosaurus. They also noted that the length of the external nares was within the known range of Tylosaurus and additionally argued that the femur being longer than the humerus was an insufficient characteristic to diagnose the species at the generic level. Based on these and other characteristics, the study found that the species cannot be referred to Hainosaurus and renamed it to Tylosaurus pembinensis. With this rediagnosis, the study also noted that the only confirmed characteristic that distinguished Hainosaurus from Tylosaurus at the time was a higher count of pygal vertebrae. It was doubted as to if this would be sufficient enough for Hainosaurus to be a distinct genus but acknowledged that further research may provide additional characteristics.[21] This further research was done in 2016 by Paulina Jimenez-Huidobro and Caldwell, which reexamined H. bernardi. They found that the unique characteristics of the type species are indeed insufficient to warrant a distinction between Hainosaurus and Tylosaurus and declared the former as a junior synonym of the latter, thus renaming H. bernardi to Tylosaurus bernardi.[30] However, this synonymization is controversial and some scientists continue to argue that Hainosaurus is a distinct genus, justified by differences in tooth morphology unexplored by Jimenez-Huidobro & Caldwell (2016) such as the presence of an advanced cutting-based dentition in T. bernardi as opposed to a more general smashing-based dentition seen in other Tylosaurus species.[114][115]
In 1896, paleontologist Armand Thevenin published a formal description of a poorly-preserved skull consisting of the majority of the maxilla, premaxilla, and dentary bones that was found in a phosphate deposit in Eclusier-Vaux, France during an earlier unspecified date. Thevenin wrote that the skull was first described by Jean Albert Gaudry, who initially thought that it belonged to a species of Liodon. However, Dollo thought that the characteristics of skull supported an alternative placement as a species of Mosasaurus. Through correspondence with Dollo and a reexamination of the skull, Thevenin noted that the rostrum was more elongated than those found in typical Mosasaurus skulls but not as long as those in the skulls of Tylosaurus or Hainosaurus. He suggested that this represented an intermediate trait for a new species, which he subsequently named Mosasaurus gaudryi; the specific epithet recognizing Gaudry's previous work on the fossil skull.[116] The skull is now on display at the French National Museum of Natural History as MNHN 1896-15. In 1990, paleontologist Theagarten Lingham-Soliar proposed reassignment of M. gaudryi to a possible species of H. bernardi based on the discovery of a double buttress supporting the suture between the premaxilla and maxilla in MNHN 1896-15, a trait he claimed that was unique to the latter species, and estimations that the rostrum may have been more elongated than preserved. This was elaborated on a publication of the same year by Nathalie Bardet of the Natural History Museum, who concluded that MNHN 1896-15 belongs to the genus Hainosaurus but as a separate species, thus changing the skull's scientific name to Hainosaurus gaudryi. This was agreed on by Lingham-Soliar in a 1992 publication.[29] In 2005, Lindgren pointed out that the characteristics used to justify the placement in Hainosaurus, such as the double buttress, can also be found in Tylosaurus. He also noted that the dentition of MNHN 1896-15 morphologically overlaps more with T. ivoensis and T. pembinensis than H. bernardi. With these characteristics, Lindgren concluded that H. gaudryi is most certainly a species of Tylosaurus, renaming it to Tylosaurus gaudryi.[17]
In 1963, paleontologist Per Ove Persson identified a new taxon of mosasaur based on isolated teeth from a deposit located in an area called Ivö Klack near Ivö Lake in Scania, Sweden. Such teeth and various other teeth pertaining to the same taxon were recovered and described from this area numerous times in the past since 1836, but they have always been misidentified as either an ichthyosaur or Mosasaurus hoffmannii. Persson proposed that the teeth belonged to a new subspecies of M. hoffmannii and gave it the name Mosasaurus hoffmannii ivoensis, the prefix ivo- in the species name referring to Ivö Klack. Russell (1967) amended this identification by elevating the taxon to a distinct species. He also identified a mosasaur fossil from the Niobrara Formation in Kansas consisting of a partial skull, some vertebrae, and a coracoid bone as being of Mosasaurus ivoensis. In an abstract presented in 1998, Lindgren doubted if M. ivoensis was a species of Mosasaurus. He instead proposed that the species was actually of Hainosaurus. The next year in 1999, Lindgren amended this in another abstract and instead suggested that the species should be moved to Tylosaurus. In 2002, he co-authored a study with paleontologist Mikael Siversson which examined the fossils referred to the species as well as new material consisting of pterygoid teeth, partial jawbones, and some vertebrae. It was found that the Niobrara fossil identified as M. ivoensis by Russell (1967) is actually of a different species. Examinations of the Swedish teeth found possible similarities with that of Taniwhasaurus, but due to the poor representation of the genus and the sheer distance between the two taxa (Taniwhasaurus was primarily known from New Zealand at the time), it was expressed that it is unlikely that M. ivoensis belongs to it. Instead, the study concluded that the species should belong to Tylosaurus and thus renamed it Tylosaurus ivoensis.[34] However, a 2008 study led by Caldwell discovered Taniwhasaurus in northern Japan, which was of similar latitude with Ivö Klack during the Cretaceous, and reasserted dental similarities between T. ivoensis and the genus. This opened the possibility that the species could be reassigned to Taniwhasaurus, but the authors considered this to be a topic for a different study.[41]
In 1964, Miguel Telles Antunes described Mosasaurus iembeensis from a partial skull excavated from the Itombe Formation near the town of Iembe, Angola.[29] In 1992, Lingham-Soliar argued that the features of the skull disagreed with those of Mosasaurus and were instead characteristic of Tylosaurus. He subsequently moved the species into the genus, becoming Tylosaurus iembeensis. However, Lingham-Soliar did not figure the holotype skull, which he identified as residing in the collections of NOVA University Lisbon without a catalog number,[29] and it was later reported in 2006 that the specimen may have been lost during a fire.[6][117] In a 2012 multi-author study led by Octávio Mateus, it was reported that an additional T. iembeensis fossil consisting of fragmentary skull elements was recovered during an expedition to the lost holotype's locality, although the specimen was not figured or formally described.[117]
21st century developments[edit]
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In the 1990s, a well-preserved mosasaur skull of uncertain identity, which was discovered in an outcrop of the Niobrara Formation in the northwestern part of Ellis County, Kansas in 1968 and cataloged in the Sternberg Museum as FHSM VP-2295, was recognized by multiple authors as being a new species of Tylosaurus. Despite such recognition, however, no paleontologist investigated this further and the fossil remained undescribed during the remainder of the 20th century. In a 2004 meeting, Everhart suggested that the new species should finally be given a scientific name and formal description, to which paleontologist Louis L. Jacobs responded with "Well, get it done."[118] In 2005, Everhart published a formal description of the new species represented by FHSM VP-2295. Thirteen different Tylosaurus specimens also from Kansas were identified as conspecific with FHSM VP-2295, and in reference to their shared localities the new species was given the name Tylosaurus kansasensis.[46] However, during a 2007 meeting, Caldwell approached Everhart and suggested that his description of T. kansasensis was not adequate enough and should be readdressed in a followup paper.[118] In 2013, Caldwell and Jiménez-Huidobro presented an abstract at the annual Society of Vertebrate Paleontology meeting casting doubt on the distinction of the species from T. nepaeolicus[118] and in 2016 the two and paleontologist Tiago Simões published a study arguing that T. kansasensis was merely a juvenile form of T. nepaeolicus, thus making the former a junior synonym of the latter.[36] This was criticized by Everhart as "poorly researched and written" in his 2017 book Oceans of Kansas; he maintained T. kansasensis as a distinct species.[118] A 2018 study by Robert F. Stewart and Jordan Mallon also rejected the synonymy based on inconsistencies when comparing the ontogenetic trends of T. kansasensis and T. nepaeolicus between the better-understood T. proriger.[38] Another ontogenetic study published in 2020 by Amelia R. Zietlow came in support of the synonymy based on results from ontograms constructed from a cladistical analysis.[23]
In 1995, the Royal Saskatchewan Museum excavated a partial skeleton first discovered a year prior by a local farmer from a hill located northwest of Herbert Ferry, Saskatchewan.[119][120] The skeleton was found articulated and consists of a "moderately complete" skull, a largely complete vertebral column, limb bones, and bones of a smaller mosasaur as stomach content;[27][119] it was curated into the museum as RSM P2588.1 and nicknamed "Omācīw" (meaning "hunter" in Cree).[119][18] In 2006, Timon Bullard of the University of Alberta studied the specimen in his Master of Science thesis. At the time, the Omācīw fossil was still in preparation and Bullard was only able to examine the right side of the skull. However, he identified that the fossil represented a new species of Tylosaurus and suggested that it be named Tylosaurus saskatchewanensis in reference to its type locality.[27] Bullard's thesis was never published but subsequently published studies recognized T. saskatchewanensis as a valid species despite technically never having been formally described.[30][41] In 2018, Bullard co-authored a multi-author study led by Jiménez-Huidobro which formally described Omācīw, which by then was more fully prepared, and confirmed its identity as a distinct species.[27]
In 2020, the MS thesis of Samuel Garvey of the University of Cincinnati was published. The thesis focused on TMP 2014.011.0001, a Tylosaurus fossil in the collections of the Royal Tyrrell Museum consisting of a partial snout and a fragment of the right mandible. The specimen was found around 55 kilometers (34 mi) northeast of Grande Prairie, Alberta; during the Cretaceous this locality was located at around 62° N, making the fossil the northernmost known occurrence of Tylosaurus and one of the few known occasions of a mosasaur existing in boreal climates. Moreover, the morphology of TMP 2014.011.0001 was recognized as very distinct from other Tylosaurus species. For example, it exhibited paedomorphosis in its teeth, which were slender and designed for piercing prey (contrary to the more robust cutting-specialized teeth of typical Tylosaurus species), a trait likely retained from juveniles. The uniqueness of the specimen led to the conclusion that it was a new species, which Garvey subsequently proposed that it be named Tylosaurus borealis in reference to its northernly occurrence.[22]
Classification[edit]
As a mosasaur, Tylosaurus is classified within the family Mosasauridae in the superfamily Mosasauroidea. The genus is the type genus of its own subfamily, the Tylosaurinae. Other members of this group include Taniwhasaurus and possibly Kaikaifilu, and the subfamily is defined by a shared feature of an elongated conical rostrum that does not bear teeth.[5] The closest relatives of the Tylosaurinae include the Plioplatecarpinae and the primitive subfamilies Tethysaurinae and Yaguarasaurinae; together they are members of one of three possible major lineages of mosasaurs (the others being the Mosasaurinae subfamily and Halisauromorpha group) that was first recognized in 1993. This clade was named the Russellosaurina by Polcyn and Bell in 2005.[121][122][123]
The evolutionary relationship between the Russellosaurina and other groups, and thus the identity of Tylosaurus as a mosasaur, remains a controversial subject. The traditional view of mosasaur evolution held that all paddle-limbed (hydropedal) mosasaurs originated from a single common ancestor with functional legs (plesiopedal). However, this was shaken with the discovery of Dallasaurus, a hydropelvic mosasauroid that was found by multiple phylogenetic analyses to be an ancestor of the Mosasaurinae but unrelated to the Russellosaurina, whose basal members included plesiopedal genera (Tethysaurinae) of their own. This meant that the Russellosaurina may have evolved a hydropedal form independently through the tethysaurines, meaning that its placement within the Mosasauridae creates a polyphyly and thus potentially invalid.[121][122] Caldwell informally proposed in a 2012 publication that the definition of a mosasaur must thus be redefined into one that does not consider russellosaurines like Tylosaurus as true mosasaurs, but as an independent group of marine lizards.[122] However, phylogenetic studies of mosasaurs can be fickle, especially given that wild card taxa like Dallasaurus remain poorly understood. For example, some studies such as a 2009 analysis by Dutchak and Caldwell instead found that Dallasaurus was ancestral to both russellosaurines and mosasaurines,[124] although results were inconsistent in later studies.[125] A 2017 study by Simoes et al. noted that utilization of different methods of phylogenetic analyses can yield different findings and ultimately found a consistent indication that tethysaurines were a case of hydropedal mosasaurs reversing back to a plesiopedal condition rather than an independent ancestral feature, suggesting that the identity of Tylosaurus as a true mosasaur was not as problematic as previously thought.[125]
Tylosaurus was among the earliest known derived mosasaurs. The oldest fossil attributed to the genus is of a skull (SGM-M1) recovered from Upper Turonian deposits of Ojinaga Formation in Chihuahua, Mexico,[2][5] which may date around 90 million years ago at earliest based on correlations with index fossils.[1] This skull has been identified as an indeterminate species with significant affinities with T. kansasensis, which was previously considered the most primitive species.[2] A tooth from a Late Maastrichtian deposit in Nasiłów, Poland dating close to the Cretaceous–Paleogene boundary has been attributed to Hainosaurus sp.[3][7] With the incorporation of Hainosaurus as a synonym of Tylosaurus, this also makes the genus one of the last mosasaurs.[30][3] Currently, eight species of Tylosaurus are recognized by scientists as taxonomically valid. They are as follow: T. proriger and T. nepaeolicus from North America, T. bernardi from Europe, T. gaudryi from France, T. ivoensis from Sweden, T. iembeensis from Angola, and T. pembinensis and T. saskatchewanensis from Canada. The validity of two additional taxa remain unsettled; there is still debate whether T. kansasensis is synonymous with T. nepaeolicus, and T. borealis has yet to be described in a formal publication.[5][22]
In the Western Interior Seaway, two species—T. nepaeolicus and T. proriger—represent a chronospecies, in which they make up a single lineage that continuously evolves without branching off in a process known as anagenesis. This is evident by how the two species do not stratigraphically overlap, are sister species, share minor and intermediate morphological differences such as a gradual change in the development of the quadrate bone, and lived in the same locations.[46][23] The means by which this lineage evolved has been hypothesized to be through one of two evolutionary mechanisms related to changes in ontogeny. First, Jiménez-Huidobro, Simões, and Caldwell proposed in 2016 that T. proriger evolved as a paedomorph of T. nepaeolicus, in which the descendant arose as a result of morphological changes through the retention of juvenile features of the ancestor in adulthood. This was based on the presence of a frontal crest and convex borders of the parietal of the skull shared in both juvenile T. nepaeolicus and all T. proriger but lost in adult T. nepaeolicus.[36][23] However, an ontogenetic study by Zietlow (2020) found that it was unclear whether this observation was a result of paedomorphosis, although this uncertainty may have been due that the sample size of mature T. nepaeolicus was too low to determine statistical significance. Second, the same study proposed an alternative hypothesis of peramorphosis, in which T. proriger evolved by developing traits found in mature T. nepaeolicus during immaturity. Based on results from a cladistical ontogram developed using data from 74 Tylosaurus specimens, the study identified a multitude of traits that were present in all T. proriger and mature T. nepaeolicus but absent in juvenile T. nepaeolicus: the skull size and depth are large, the length of the elongated rostrum exceeds 5% of the total skull length, the quadrate suprastapedial processes are thick, the overall quadrate shape converges, and the posteroventral process is fan-like.[23]
The following cladogram is modified from a phylogenetic analysis by Jiménez-Huidobro & Caldwell (2019) using Tylosaurus species with sufficiently known material to model accurate relationships; T. gaudryi, T. ivoensis, and T. iembeensis were too poorly understood to be added into the analysis.[5]
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Paleobiology[edit]
Growth and development[edit]
Metabolism[edit]
Nearly all squamates are characterized by their cold-blooded ectothermic metabolism, but mosasaurs like Tylosaurus are unique in that they were likely endothermic, or warm-blooded.[126] The only other known lizard with such a trait is the Argentine black and white tegu, though only partially.[127] Endothermy in Tylosaurus was proven in a 2016 study by Harrell, Pérez‐Huerta, and Suarez by examining δ18O isotopes in Tylosaurus bones. δ18O levels can be used to calculate the internal body temperature of animals, and by comparing such calculated temperatures between coexisting cold-blooded and warm-blooded animals, the type of metabolism can be inferred. The study used the body temperatures of the cold-blooded fish Enchodus and sea turtle Toxochelys (correlated with ocean temperatures) and warm-blooded seabird Ichthyornis from the Mooreville Chalk as a proxy. Analyzing the isotope levels of eleven Tylosaurus specimens an average internal body temperature of 34.3 °C (93.7 °F) was calculated. This was much higher than the body temperature of Enchodus and Toxochelys (28.3 °C (82.9 °F) and 27.2 °C (81.0 °F) respectively) and similar to that of Ichthyornis (38.6 °C (101.5 °F)). Harrell, Pérez‐Huerta, and Suarez also calculated the body temperatures of Platecarpus and Clidastes with similar numbers, 36.3 °C (97.3 °F) and 33.1 °C (91.6 °F) respectively. The fact that the other mosasaurs were much smaller in size than Tylosaurus and yet maintained similar body temperatures made it unlikely that Tylosaurus's body temperature was the result of another metabolic type like gigantothermy. Endothermy would have provided several advantages to Tylosaurus such as increased stamina for foraging larger areas and pursuing prey, the ability to access colder waters, and better adaptation to withstand the gradual cooling of global temperatures during the Late Cretaceous.[126]
Mobility[edit]
Scientists previously interpreted Tylosaurus as an anguilliform swimmer that moved by undulating its entire body like a snake due to its close relationship with the animal. However, it is now understood that Tylosaurus actually used carangiform locomotion, meaning that the upper body was less flexible and movement was largely concentrated at the tail like in mackerels. A BS thesis by Jesse Carpenter published in 2017 examined the vertebral mobility of T. proriger spinal columns and found that the dorsal vertebrae were relatively rigid but the cervical, pygal, and caudal vertebrae were more liberal in movement, indicating flexibility in the neck, hip, and tail regions. This contrasted with more derived mosasaurs like Plotosaurus, whose vertebral column was stiff up to the hip. Interestingly, an examination of a juvenile T. proriger found that its cervical and dorsal vertebrae were much stiffer than those in adult specimens. This may have been an evolutionary adaptation among young individuals; a more rigid tail-based locomotion is associated with faster speed, and this would allow vulnerable juveniles to better escape predators or catch prey. Older individuals would see their spine grow in flexibility as predator evasion becomes less important for survival.[128]
Tylosaurus likely specialized as an ambush predator. It was lightweight for a mosasaur of its size, having a morphological build designed to vastly reduce body mass and density. Its pectoral and pelvic girdles and paddles, which are associated with weight, are proportionally small. Its bones were highly cancellous and were likely filled with fat cells in life, which also increased buoyancy. It is unlikely that the latter trait was evolved in response to increasing body size as the similarly-sized Mosasaurus hoffmannii lacked highly cancellous bone. These traits allowed Tylosaurus to be more conservative in its energy requirements, which is useful when traveling between ambush sites over large distances or through stealth. In addition, a reduced body density likely helped Tylosaurus to rapidly accelerate during an attack, assisted with the long and powerful tail of the mosasaur.[29]
A 1988 study by Judith Massare attempted to calculate the sustained swimming speed, the speed at which the animal moves without tiring, of Tylosaurus through a series of mathematical models incorporating hydrodynamic characteristics and estimations of locomotive efficiency and metabolic costs. Using two T. proriger specimens, one 6.46 meters (21.2 ft) long and the other 6.32 meters (20.7 ft), she calculated a consistent average maximum sustained swimming speed of 2.32 m/s (5.2 mph). However, when testing whether the models represented an accurate framework, they were found to exaggerated. This was primarily because the variables accounting for drag may have been underestimated; estimation of drag coefficients for an extinct species can be difficult as it requires a hypothetical reconstruction of the morphological dimensions of the animal. Massare predicted that the actual sustained swimming speed of Tylosaurus was somewhere near half the calculated speed.[129] The mathematical framework was subsequently corrected and modified for accuracy in 2002 by Ryosuke Motani, but Tylosaurus was not examined in the study.[130]
Senses[edit]
Feeding[edit]
One of the largest marine carnivores of its time, Tylosaurus was an apex predator that exploited the wide variety of marine fauna in its ecosystem. Stomach contents are well documented in the genus, which includes other mosasaurs, plesiosaurs, turtles, birds, bony fish, and sharks.[131] Additional evidence from bite marks suggests the animal also preyed on giant squid[132] and ammonites.[133]
The enormous and varied appetite of Tylosaurus can been demonstrated in a 1987 find that identified fossils of a mosasaur measuring 2 meters (6.6 ft) or longer, the diving bird Hesperornis, a Bananogmius fish, and possibly a shark all within the stomach of a single T. proriger skeleton (SDSM 10439) recovered from the Pierre Shale of South Dakota.[l][29][131][136] Other records of stomach contents include a sea turtle in a T. bernardi-like species,[m][131] a 2.5 meters (8.2 ft) long Dolichorhynchops in another T. proriger,[131] partially digested bones and scales of a Cimolichthys in a third T. proriger,[134] partially digested vertebrae of a Clidastes in a fourth T. proriger, remains of three Platecarpus individuals in a T. nepaeolicus,[13] and Plioplatecarpus bones in a T. saskatchewanensis.[119][137] Puncture marks on fossils of ammonites,[133] the carapace of a Protostega,[138] and the gladius of an Enchoteuthis have been attributed to Tylosaurus.[132]
Pasch and May (2001) reported bite marks from a dinosaur skeleton known as the Talkeetna Mountains Hadrosaur, which was found in marine strata of the Turonian-age Matanuska Formation in Alaska. The features of these marks were found to closely match that of the teeth of T. proriger. Because the fossil's locality was of marine deposits, the study reasoned that the dinosaur must have drifted offshore as a bloat-and-float carcass that was subsequently scavenged by the mosasaur. It was unlikely that the marks were a result of predation, as that would have led to a puncture, preventing the buildup of the bloating gases that allowed the corpse to drift out to sea in the first place.[139] Garvey (2020) criticized the lack of conclusive evidence to support this hypothesis and ruled out T. proriger as a possible culprit, given that the species did not appear until the Santonian and is exclusive to the Western Interior Seaway.[22] However, close relatives did maintain a presence nearby, evidenced by fragmentary fossils of an indeterminate tylosaurine from Turonian deposits in the Russian Chukotsky District.[140]
Social behavior[edit]
The behavior of Tylosaurus towards each other may have been mostly aggressive, evidenced by fossils with injuries inflicted by another of their own kind. Such remains were frequently reported by fossil hunters during the late 19th and early 20th centuries, but few examples reside as specimens in scientific collections. Many of these fossils consist of healed bite marks and wounds that are concentrated around or near the head region, implying that there were the result of non-lethal interaction, but the motives of such contact remain speculative. In 1993, Rothschild and Martin noted that some modern lizards affectionatly bite their mate's head during courtship, which can sometimes result in injuries. Alternatively, they also observed that some males lizards also employ head-biting as territorial behavior against rivals in a show of dominance by grappling the head to turn over the other on its back. It is possible that Tylosaurus behaved in similar ways.[13]
Lingham-Soliar (1992) mentioned the consideration that the use of the combat-oriented elongated rostrum of Tylosaurus was not exclusive to hunting and that it may have also been applied in sexual behavior through battles over female mates between males.[29] However, the study observed the elongated rostrum was invariably present in all individuals regardless of sex,[29] and subsequent studies by Konishi et al. (2018) and Zietlow (2020) confirmed this pattern.[42][23] This would imply that sexual selection was not a driver in its evolution and instead refined through sex-independant means.[42]
At least one fatal instance of intraspecific combat among Tylosaurus is documented. This can be seen in the T. kansasensis holotype FHSM VP-2295, representing a 5 meters (16 ft) long animal, which possesses numerous injuries that indicate it was killed by a larger Tylosaurus. The skull roof and surrounding areas exhibit signs of trauma in the form of four massive gouges, and the dentary contains at least seven puncture wounds and gouges. These pathologies are unequivocally characteristic of bite marks from a larger Tylosaurus that measured around 7 meters (23 ft) in length. The largest of the marks are about 4 centimeters (1.6 in) in length, matching the size of large mosasaur teeth, and they are positioned along two lines that converge close to 30°, matching the angle that each jaw converges towards in a mosasaur skull. In addition, FHSM VP-2295 suffered damage to the sclerotic ring, a detached quadrate, and an articulation of the cervical vertebrae at an unnatural angle of 40° to the skull's long axis. The pattern of preservation makes it unlikely that the condition of the vertebrae was a result of disturbances by scavengers and instead indicates damage caused by a violently twisted neck during life. In a reconstructed scenario, the larger Tylosaurus would have first attacked at an angle slightly below the left side of the vicitim's head. This impact would cause the victim's skull to roll to the right side, allowing the aggressor to sink its teeth into the skull roof and right lower jaw, the latter leading to the collapse of the jawbone, further breaks of nearby bones such as the pterygoid, a break in the right eye, and the twisting of the jawbone outwards. This would subsequently cause the quadrate to detach from its position and the spinal cord to twist and sever at the skull's base, leading to a swift death.[13]
Paleopathology[edit]
Examining 12 North American Tylosaurus skeletons and one T. bernardi skeleton, Rothschild and Martin (2005) identified evidence of avascular necrosis in every individual. For aquatic animals, this condition is often a result of decompression illness, which is caused when bone-damaging nitrogen bubbles build up in inhaled air that is decompressed either by frequent deep-diving trips or by intervals of repetitive diving and short breathing. The studied mosasaurs likely gained avascular necrosis through such behaviors, and given its invariable presence in Tylosaurus it is likely that deep or repetitive diving was a general behavioral trait of the genus. The study observed that between 3-15% of vertebrae in the spinal column of North American Tylosaurus and 16% of vertebrae in T. bernardi were affected by avascular necrosis.[141] Carlsen (2017) posited that Tylosaurus gained avascular necrosis because it lacked the necessary adaptations for deep or repetitive diving, although noted that the genus had well-developed eardrums that could protect themselves from rapid changes in pressure.[142]
Unnatural fusion of some vertebrae in the tail has been reported in some Tylosaurus skeletons. A variation of these fusions may concentrate near the end of the tail to form a single mass of multiple fused vertebrae called a "club tail." Rothschild and Everhart (2015) surveyed 23 North American Tylosaurus skeletons and one T. bernardi skeleton and found that five of the North American skeletons exhibited fused tail vertebrae. The condition was not found in T. bernardi, but this does not rule out its presence due to the low sample size. Vertebral fusion occurs when the bones remodel themselves after damage from trauma or disease. However, the cause of such events can vary between individuals and/or remain hypothetical. One juvenile specimen with the club tail condition was found with a shark tooth embedded in the fusion, which confirms that at least some cases were caused by infections inflicted by predator attacks. The majority of vertebral fusion cases in Tylosaurus were caused by bone infections, but some cases may have alternatively been caused by any type of joint disease such as arthritis. However, evidence of joint disease was rare in Tylosaurus when compared to mosasaurs such as Plioplatecarpus and Clidastes.[143] Similar amassing of remodeled bone is also documented in bone fractures in other body parts. One T. kansasensis specimen possesses two fractured ribs that fully healed. Another T. proriger skull shows a fractured snout, probably caused by ramming into a hard object such as a rock. Presence of some healing indicates that the individual survived for some extended time before death. The injury in a snout region containing many nerve endings would have inflicted extreme pain.[144]
Paleoecology[edit]
Range and ecosystem[edit]
Throughout its ~20 million-year history, Tylosaurus was endemic to the North Atlantic Circle Basin, a geographic region comprising the North Atlantic and neighboring waters including the Western Interior Seaway in North America and Mediterranean Tethys in Europe above 30°N.Cite error: The <ref> tag name cannot be a simple integer (see the help page). Much of the region was encompassed by a temperate ocean climate. Localities where fossils have been found within there include the United States, Canada, Mexico, Belgium, France, Poland, Sweden, Germany, England, and possibly Spain. There are a few exceptions of occurrences in warmer low-latitude zones in scientific literature. This includes T. iembeensis from the Coniacian of Angola[145] and an isolated tooth from Maastrichtian deposits in the Democratic Republic of the Congo identified as 'Hainosaurus.' It has been suggested that tylosaurines like Tylosaurus may have been present in Maastrichtian waters of Morocco given its location within the Mediterranean Tethys and ecological diversity as a mosasaur hotspot, where a current lack of reliable fossil evidence in the area is likely due to sampling bias for a mosasaur that was generally rare around that time.Cite error: The <ref> tag name cannot be a simple integer (see the help page).
North America[edit]
Around the beginning of the Middle Campanian around 80 mya, Tylosaurus experienced an sharp decline in diversity, where abundant species like T. proriger suddenly went extinct and the genus disappeared from most of the Western Interior Seaway. This coincided with a larger continental extinction event called the Niobraran-Navesinkan turnover, during which the mosasaur biodiversity making up a preceding "Niobraran Age" collapsed and was replaced by a new assemblage of "Navesinkan Age" fauna. The causes of this event remains unknown, but scientists have noted that the shift to the Navesinkan Age coincides with a decrease in ocean temperatures.Cite error: The <ref> tag name cannot be a simple integer (see the help page). It was initially suggested by Russell (1994) that a meteor that struck what is now Manson, Iowa was a possible trigger, but this was based on a misdating of the impact event.Cite error: The <ref> tag name cannot be a simple integer (see the help page). In her 2002 doctoral thesis at the University of Cincinnati, Janet Bertog suggested that a combination of global sea level falls and increased regional tectonic activity such as the mountain-forming Sevier orogeny may have contributed to the turnover.Cite error: The <ref> tag name cannot be a simple integer (see the help page). Only T. saskatchewanensis and a close relative in Canada survived the event and persisted longer into the Campanian.
Europe[edit]
Africa[edit]
Habitat preference[edit]
Competition[edit]
The causes behind this global event remains unknown. Russell (1994) previously suggested
Old junk[edit]
A distinguishing characteristic of Tylosaurus is its elongated, cylindrical premaxilla (snout) from which it takes its name. Unlike other mosasaurs, Tylosaurus did not have teeth all the way forward on its premaxilla, as the bony protuberance was free of teeth.[146] Tylosaurus also have 24 to 26 teeth in the upper jaw, 20 to 22 teeth on the palate, 26 teeth on the lower jaw, 29 to 30 vertebrate between the skull and hip, 6 to 7 vertebrae in the hip, 33 to 34 vertebrae in the tail with chevrons, and a further 56 to 58 vertebrae making up the tip of the tail.[147]
Growth[edit]
Konishi and colleagues in 2018 assigned specimen FHSM VP-14845, a small juvenile with an estimated skull length of 30 centimeters (12 in), to Tylosaurus based on the proportions of the braincase and the arrangement of the teeth in the snout and on the palate. However, the specimen lacks the characteristic snout projection of other Tylosaurus, which is present in juveniles of T. nepaeolicus and T. proriger with skull lengths of 40–60 cm (16–24 in). This suggests that Tylosaurus acquired the snout projection rapidly at an early stage in life, and also suggests that it did not develop due to sexual selection. Konishi and colleagues suggested a function in ramming prey, as employed by the modern orca.
Footnotes[edit]
- ^ From the Ancient Greek τύλος (týlos, "protuberance, knob") + σαῦρος (saûros, "lizard")
- ^ Some individuals will occasionally have tooth counts slightly outside this range.[23]
- ^ Inconsistent in T. proriger.[23]
- ^ Behind the fifth tooth in the holotype.[46]
- ^ Nasals were initially identified in the holotype of Eonatator,[48] but later found to be a plaster restoration.[49]
- ^ In one juvenile T. proriger specimen, it appears at the bottom of the vertical ramus instead.[36]
- ^ The odontoid is present in the atlas instead of the axis in lizards.[60]
- ^ Jiménez-Huidobro and Caldwell (2016) chose to not completely follow this presumption and reported the cervical count for T. bernardi as "6 or 7."[30]
- ^ Jiménez-Huidobro and Caldwell (2016) chose to not completely follow this presumption and reported the cervical count for T. bernardi as "6 or 7."[30]
- ^ Latter corresponds to the fifth rib in Osborn (1899).[73]
- ^ Cope compared the length of T. dyspelor to that of a "great finner whale",[93] which was the common name of the taxon Balaenoptera sibbaldii at the time.[97] This taxon is a synonym of the modern blue whale Balaenoptera musculus.[98]
- ^ Identification of the mosasaur and shark vary. Scientists have identified the mosasaur as either a Platecarpus,[13] Clidastes,[134] or Latoplatecarpus.[131] The shark is either interpreted as a Cretalamna,[134] a sand shark,[135] or of uncertain identity.[131]
- ^ Usually identified as Hainosaurus sp.;[131] Lingham-Soliar (1992) identifies the species as T. bernardi.[29]
References[edit]
- ^ a b Ogg, J.G.; Hinnov, L.A. (2012). Cretaceous. pp. 793–853. doi:10.1016/B978-0-444-59425-9.00027-5. ISBN 9780444594259.
{{cite book}}:|journal=ignored (help) - ^ a b c d Flores, A.L. (2013). "Occurrence of a tylosaurine mosasaur (Mosasauridae; Russellosaurina) from the Turonian of Chihuahua State, Mexico" (PDF). Boletín de la Sociedad Geológica Mexicana. 65 (1): 99–107.
- ^ a b c Jagt, J.W.M.; Lindgren J.; Machalski, M.; Radwański, A. (2005). "New records of the tylosaurine mosasaur Hainosaurus from the Campanian-Maastrichtian (Late Cretaceous) of central Poland". Netherlands Journal of Geosciences. 84 (Special Issue 3): 303–306. doi:10.1017/S0016774600021077.
- ^ a b c d Hornung, J.J.; Reich, M. (2015). "Tylosaurine mosasaurs (Squamata) from the Late Cretaceous of northern Germany". Netherlands Journal of Geosciences. 94 (1): 55–71. doi:10.1017/njg.2014.31.
- ^ a b c d e f g h i j k l m n o p q r s Jiménez-Huidobro, P.; Caldwell, M.W. (2019). "A New Hypothesis of the Phylogenetic Relationships of the Tylosaurinae (Squamata: Mosasauroidea)" (PDF). Frontiers in Earth Science. 7 (47). doi:10.3389/feart.2019.00047.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ a b Jacobs, L.L.; Mateus, O.; Polcyn, M.J.; Schulp, A.S.; Antunes, M.T.; Morais, M. L.; Tavares, T.S. (2006). "The occurrence and geological setting of Cretaceous dinosaurs, mosasaurs, plesiosaurs, and turtles from Angola" (PDF). Paleontological Society of Korea. 22 (1): 91–110.
- ^ a b Keutgen, N.; Remin, A.; Jagt, J.W.M. (2017). "The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) – taxonomy and palaeobiological implications". Palaeontologia Electronica. 20.2.38A: 1–29. doi:10.26879/671.
- ^ a b c d e f g h i Everhart, M.J. (2002). "New Data on Cranial Measurements and Body Length of the Mosasaur, Tylosaurus nepaeolicus (Squamata; Mosasauridae), from the Niobrara Formation of Western Kansas". Transactions of the Kansas Academy of Science. 105 (1–2): 33–43. doi:10.1660/0022-8443(2002)105[0033:NDOCMA]2.0.CO;2.
- ^ Everhart, M.J.; Jagt, J.W.M.; Mulder, E.W.A.; Schulp, A.S. (2016), Mosasaurs–how large did they really get? 5th triennial Mosasaur meeting—a global perspective on Mesozoic marine amniotes, Uppsala, 16–20 May 2016, Program and Abstracts, Museum of Evolution. Uppsala. Uppsala University. pp. 8-10
- ^ Everhart 2017, p. 214.
- ^ Everhart 2017, p. 192.
- ^ Everhart, M.J. (2005). "Rapid evolution, diversification and distribution of mosasaurs (Reptilia; Squamata) prior to the KT Boundary". Tate 2005 11th Annual Symposium in Paleontology and Geology.
- ^ a b c d e Everhart, M.J. (2008). "A bitten skull of Tylosaurus kansasensis (Squamata: Mosasauridae) and a review of mosasaur-on-mosasaur pathology in the fossil record". Transactions of the Kansas Academy of Science. 111 (3/4): 251–262. doi:10.1660/0022-8443-111.3.251.
- ^ Everhart, M.J. (2004). "Plesiosaurs as the food of mosasaurs; new data on the stomach contents of a Tylosaurus proriger (Squamata; Mosasauridae) from the Niobrara Formation of western Kansas". The Mosasaur. 7: 41–46.
- ^ Everhart 2017, p. 213.
- ^ Everhart 2017, p. 215.
- ^ a b c d Lindgren, J. (2005). "The first record of Hainosaurus (Reptilia: Mosasauridae) from Sweden". Journal of Paleontology. 79 (6): 1157–1165. doi:10.1666/0022-3360(2005)079[1157:tfrohr]2.0.co;2.
- ^ a b "Hunter of the prairie sea" (PDF). Royal Saskatchewan Museum.
- ^ "Largest mosasaur on display". Guinness World Records. Retrieved 2020-06-03.
- ^ CBC News (2008-08-27). "Manitoba dig uncovers 80-million-year-old sea creature". CBC. Manitoba. Archived from the original on 2018-06-05.
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y Bullard, T.S.; Caldwell, M.W. (2010). "Redescription and rediagnosis of the tylosaurine mosasaur Hainosaurus pembinensis Nicholls, 1988, as Tylosaurus pembinensis (Nicholls, 1988)". Journal of Vertebrate Paleontology. 30 (2): 416–426. doi:10.1080/02724631003621870.
- ^ a b c d e f Garvey, S.T. (2020). A new high-latitude Tylosaurus (Squamata, Mosasauridae) from Canada with unique dentition (MS). University of Alberta.
- ^ a b c d e f g h i j k l m n o p q r s t u Zietlow, A.R. (2020). "Craniofacial ontogeny in Tylosaurinae". PeerJ. 8: e10145. doi:10.7717/peerj.10145.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ Christiansen, P.; Bonde, M. (2002). "A new species of gigantic mosasaur from the Late Cretaceous of Israel". Journal of Vertebrate Paleontology. 22 (3): 629–644. doi:10.1671/0272-4634(2002)022[0629:ANSOGM]2.0.CO;2.
- ^ Russell 1967, p. 14.
- ^ a b Nicholls, E.L. (1988). "The first record of the mosasaur Hainosaurus (Reptilia: Lacertilia) from North America". Canadian Journal of Earth Sciences. 25 (10): 1564–1570. doi:10.1139/e88-149.
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa Jiménez-Huidobro, P.; Caldwell, M.W.; Paparella, I.; Bullard, T.S. (2018). "A new species of tylosaurine mosasaur from the upper Campanian Bearpaw Formation of Saskatchewan, Canada". Journal of Systematic Palaeontology: 1–16. doi:10.1080/14772019.2018.1471744.
- ^ Russell 1967, p. 50.
- ^ a b c d e f g h i j k l m n o p q r s t u Lingham-Soliar, T. (1992). "The Tylosaurine Mosasaurs (Reptilia, Mosasauridae) from the Upper Cretaceous of Europe and Africa". Bulletin de l’Institut Royal des Sciences Naturelles de Belgique, Sciences de la Terre. 62: 171–194.
- ^ a b c d e f g h i j k l m n o p q r s t u Jiménez-Huidobro, P.; Caldwell, M.W. (2016). "Reassessment and reassignment of the early Maastrichtian mosasaur Hainosaurus bernardi Dollo, 1885, to Tylosaurus Marsh, 1872". Journal of Vertebrate Paleontology. 36 (3): e1096275. doi:10.1080/02724634.2016.1096275.
- ^ a b Russell 1967, p. 43.
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- Bell GL. Jr. 1997. Part IV: Mosasauridae - Introduction. pp. 281–292 In: Callaway J. M. and E. L Nicholls, (eds.), Ancient Marine Reptiles, Academic Press, 501 pages.
- Everhart MJ. 2001. Revisions to the biostratigraphy of the Mosasauridae (Squamata) in the Smoky Hill Chalk Member of the Niobrara Chalk (Late Cretaceous) of Kansas. Transactions of the Kansas Academy of Science 104 (1-2): 56–75.
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- Everhart MJ. 2005. Oceans of Kansas - A Natural History of the Western Interior Sea. Indiana University Press, 322 pp.
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Cited books[edit]
- Ellis, R. (2003). Sea Dragons: Predators of the Prehistoric Oceans. University Press of Kansas. ISBN 978-0700613946.
- Everhart, M.J. (2017). Oceans of Kansas, Second Edition: A Natural History of the Western Interior Sea (Life of the Past). Indiana University Press. ISBN 978-0253026323.
- Leidy, J. (1873). Contributions to the extinct vertebrate fauna of the western interior territories: Report of the United States Geological Survey of the Territories. U.S. Government Printing Office. doi:10.5962/bhl.title.61805.
- Mann, J.; Conner, R.C.; Tyack, P.L.; Whitehead, H. (2000). Cetacean Societies: Field Studies of Dolphins and Whales. University of Chicago Press. ISBN 978-0226503417.
- Russell, D.A. (1967). Systematics and Morphology of American Mosasaurs (PDF). Vol. 23. Bulletin of the Peabody Museum of Natural History. ISBN 978-1933789446.
External links[edit]
- Oceans of Kansas; includes much additional information and many illustrations and photographs of tylosaurines, including restorations and skeletons.
- E.D. Cope's original description of Macrosaurus proriger from western Kansas, with the published figure (1870) and recent photographs.
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