Thalattoarchon

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Thalattoarchon
Temporal range: Middle Triassic, Late Anisian, 244.6–242  Ma
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Thalattoarchon Holotype FMNH.jpg
Holotype skull (FMNH PR 3032)
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Ichthyosauria
Genus: Thalattoarchon
Fröbisch et al., 2013
Type species
Thalattoarchon saurophagis
Fröbisch et al., 2013

Thalattoarchon is a genus of large, Middle Triassic predatory ichthyosaur from North America, containing the single species T. saurophagis. The taxon was described in 2013 from a single specimen discovered in the Favret Formation in Nevada. The generic name, meaning "ruler of the seas", refers to its status as an apex predator, while the specific epithet, meaning "lizard eater", alludes to its carnivorous diet. The classification of this genus within the ichthyosaurs is much debated, being either classified within the clade Merriamosauria or in the more basal family Cymbospondylidae.

Contents

As an ichthyosaur, Thalattoarchon had flippers for limbs and a fin on the tail. The size of this large ichthyosaur is estimated around 8.6 meters (28 ft) long, although the authors are uncertain about the exact measurements. The animal has a long, slender body but with a proportionally large head and a straight, elongated tail. The jaws of Thalattoarchon feature large teeth with two cutting edges of up to 12 centimeters (0.39 ft), which would have been well suited for attacking large prey. Although the fossils are incomplete, it is estimated that the animal would have had a skeleton comprising at least 60 presacral vertebrae. Thalattoarchon would have been an apex predator, its sharp and cutting teeth suggesting that it would have mainly preyed on contemporary marine reptiles. Its position as a apex predator is generally comparable to that of orcas, which have a similar lifestyle.

Discovery and naming

The only specimen of Thalattoarchon was discovered in 1997 by the paleontologist Jim Holstein during a field expedition in the Augusta Mountains, located in Nevada, United States. [1] It was with the support and a grant from the National Geographic Society that the fossils were completely exhumed in 2008, [1] [2] [lower-alpha 1] after a period of work of three weeks. The recovered material was transported by a helicopter and a truck out of the field. [3] The fossils were excavated in the Taylori Zone of the Fossil Hill Member in the Favret Formation, dating to approximately 244.6 million years ago, from the beginning of the late Anisian of the Middle Triassic. The specimen, cataloged as FMNH PR 3032, consists of a major part of the skull and the axial skeleton, including parts of the pelvic girdle and rear flippers. [1]

It was in 2013 that this specimen was designated as the holotype of a new genus and species of ichthyosaurs by Nadia B. Fröbisch, Jörg Fröbisch, P. Martin Sander, Lars Schmitz and Olivier Rieppel, under the name of Thalattoarchon saurophagis in the scientific journal Proceedings of the National Academy of Sciences . The genus name comes from Ancient Greek θάλασσα (thálassa, "sea"), and ἄρχον (árchon, "ruler"), [1] directly referencing the animal's imposing size and position as an apex predator of the Triassic seas. [3] The specific name also comes from Ancient Greek and is derived from the words σαῦρος (saûros, "lizard") and φᾰγεῖν (phageîn, "to eat"), in reference to its carnivorous diet. [1] [4]

Description

Life restoration and size comparison of a T. saurophagis with a human Thalattoarchon saurophagis.jpg
Life restoration and size comparison of a T. saurophagis with a human

The describing team estimates the size of Thalattoarchon at over 8.6 meters (28 ft) long, making it one of the largest known ichthyosaurs. Its size and morphology are similar to some species of the contemporary genus Cymbospondylus . [1] [2] [3] However, due to some missing parts of the holotype specimen, the authors mentioned that the estimate could be revised when more is known about the animal. [1] In 2021, Paul Martin Sander and colleagues proposed that the animal would reach a body mass of 4.3 metric tons (4.7 short tons). [5] Like all other ichthyosaurs, Thalattoarchon has four flippers, but unlike the more derived (advanced-diverging) representatives dating from the Jurassic and Cretaceous, it has a long, poorly developed caudal fin, unlike the two caudal lobes present in later ichthyosaurs. The animal's head is remarkably large in proportion to its body, a trait rarely observed in representatives of the group. [1] The size of the skull is estimated at 1.2 meters (3.9 ft) long. [4] The skull of Thalattoarchon is proportionally shorter but more robust than those of other ichthyosaurs. [6]

Skull

The skull of the only specimen of Thalattoarchon is partially preserved, missing the entire rostrum and the front of the mandible. The rest is still well preserved and allows it to be viewed as a whole. The eye sockets are elongated, reaching up to 29 cm (11 in), and each contain a sclerotic ring. The superior temporal fenestrae are large and oval, sharing a similar shape to those of Shastasaurus . The maxillae extend well below the eye sockets and carry large teeth all the way to their posterior ends. [1] The nasal bones are very extensive and come into contact with the postorbital bones, but do not extend as far as the superior temporal fenestrae. The frontal bones are smaller, forming the anteromedial edge of the superior temporal fenestrae and surrounding the pineal foramen. In front of the pineal foramen there is a small sagittal crest that takes on the shape of a large plate further back. The parietal bones are smaller than the frontal bones and medially form the superior temporal fenestrae. The lacrimal bones and jugal bones are narrow and slender in shape. [4]

The palate, although partially preserved, appears to be dominated by the large pterygoid bones. In the lower jaw, the dentary bone extends to the level of the maxillae but apparently lacks teeth on its rearmost part. This means that at least the fifth or sixth tooth in the maxillae would be missing a facing tooth in the mandible. The surangular has a distinct coronoid process located posterior to the eye sockets. [4] Although the only known teeth of Thalattoarchon are located at the posterior level of the maxillae, it is possible that their size would increase towards the middle of the jaws. This morphological trend is also observed in many ichthyosaurs and other now extinct marine reptiles, such as mosasaurs, thalattosuchians and pliosaurs. The largest preserved tooth is at least 12 cm (4.7 in) long, with the crown alone measuring 5 cm (2.0 in). The teeth represent one of the main autapomorphies of Thalattoarchon, being large and thin, having two sharp edges each and a fairly smooth crown. The related genus Himalayasaurus has very similar dentition, but the latter differs from Thalattoarchon by the presence of longitudinal grooves on the crown. [1]

Postcranial skeleton

Although the total number of vertebrae is not known in the animal, it is estimated that it would have had at least 60 in the presacral column. The anterior dorsal vertebrae are almost round in anteroposterior view and measure 10 cm (3.9 in) in diameter and 6 cm (2.4 in) long. This latter measurement remains constant throughout the presacral column as well as in the most anterior caudal vertebrae, except at the level of the middle dorsal vertebrae, which reach 12 cm (4.7 in) in diameter. The neural spines of the anterior dorsal vertebrae are larger than the vertebrae themselves, measuring 13–14 cm (5.1–5.5 in) tall, being flattened laterally, and not sharing spaces when viewed from the sides. The anterior dorsal vertebrae are associated with ribs having only a single head, unlike the double-headed ribs present in the cervical vertebrae. The posterior dorsal vertebrae are the same height and length as the middle dorsal vertebrae. However, the latter are characterized for having a flattened ventral surface and articular facets for the double-headed ribs, a trait also observed in some basal ichthyosaurs and in neoichthyosaurians dating from the Late Triassic to the Cretaceous. [4]

The caudal vertebrae of Thalattoarchon are laterally flattened and are twice as tall as they are wide, gradually decreasing in length. Large facets for the haemal arches, or chevrons, are present on the anterior caudal vertebrae. The animal's tail appears to be rather straight, having visibly no curvature and not having a turned-down end. [4]

Few bones are preserved in the pelvic girdle and hind limbs, the only one fully preserved being the right ilium. The end of this bone participating in the hip socket is similar to that of Cymbospondylus, but its articulations with the sacral ribs may have been rather weak, as suggested by its pointed upper end. The femur is flattened and broad, having a slightly narrowed body and an enlarged distal end, being on the whole broader than that of Cymbospondylus. Another preserved bone is interpreted as a zeugopodial element (the part of a limb corresponding to either a forearm or a leg), but it is uncertain whether it is a tibia or a fibula. Regardless, it has a concave margin, enlarged ends, and is wider than long. The hind limbs and the pelvic girdle are proportionally small in relation to the body of the animal, with just the length of the femur being twice the height of the caudal vertebrae. [4]

Classification

In the phylogenetic analyses published by Fröbisch and colleagues in 2013, Thalattoarchon was classified as a basal representative of the Merriamosauria clade, being seen as more derived than Cymbospondylus and the Mixosauridae. Thalattoarchon was recovered either in an unresolved polytomy with Besanosaurus , Californosaurus , Toretocnemus , and other merriamosaurs or as more derived than the former three taxa but basal to the other merriamosaurs. [4] [1] However, in 2015, a phylogenetic revision carried out on the ichthyopterygians by Cheng Ji and his colleagues moved Thalattoarchon within the Cymbospondylidae, i.e. in a more basal position than the Merriamosauria as proposed two years earlier. [7] This classification was generally accepted and retained in several phylogenetic analyses concerning ichthyosaurs published since. [8] [9] [10] [11] In a study published in 2017, Benjamin C. Moon presented various analyses that yielded different phylogenetic positions for Thalattoarchon. These positions varied, indicating that Thalattoarchon might be more closely related to later-evolving ichthyosaurs, situated earlier in the lineage than Cymbospondylus, or classified as the sister taxon to C. nichollsi. [9] In 2021, Sander and his colleagues reclassified Thalattoarchon within the Merriamosauria, but this time as the sister taxon of the Shastasauridae. [12] [5]

The following cladogram shows the position of Thalattoarchon within the Ichthyosauromorpha after Sander et al. (2021): [12] [5]

Ichthyosauromorpha

Paleobiology

Due to its bicarinate, cutting teeth and its large, robust head, Thalattoarchon is recognized as having been an apex predator. The abundant presence of marine reptiles within the Favret Formation suggests that the animal would have regularly attacked them. Its position as an apex predator is comparable to that of current orcas, because its cutting teeth would have been adapted to attack prey of considerable size, possibly even larger than Thalattoarchon itself, in the same way as killer whales. [1] [2] [3] [6] However, large ichthyosaurs like Cymbospondylus would not have been Thalattoarchon's primary target; the generally preferred prey would be medium-sized marine reptiles or juveniles instead. [4] In 2021, Sander and his colleagues suggested that if Thalattoarchon would have fed on Cymbospondylus, it would have preyed on it using a pack-hunting strategy, a behavior that is not at all reported in the fossil record. The authors of this study also suggest that Thalattoarchon would have only fed on smaller animals, both alive and dead, a feeding strategy comparable to that of the great white shark. Due to its apex predator adaptations, Thalattoarchon would not likely feed on ammonites, squid, or even fish. [5]

Palaeoecology

Life restoration of a Cymbospondylus swimming near a group of Phalarodon, two ichthyosaurs contemporary with Thalattoarchon Cymbospondylus and Phalarodon.jpg
Life restoration of a Cymbospondylus swimming near a group of Phalarodon , two ichthyosaurs contemporary with Thalattoarchon

Thalattoarchon is known from the Favret Formation, which, along with the Prida Formation, constitutes one of two recognized geological formations of the Star Peak Group, located in Nevada. These two formations are linked by a single member, known as the Fossil Hill Member. In the Prida Formation, this member outcrops west of the Humboldt Range, and extends to the Favret Formation, outcropping in the Augusta Mountains, [13] where it reaches up to more than 300 metres (980 ft) wide. [14] [5] Although they are neighbors, the two formations do not share precisely the same age, the Prida one dating from the Middle Anisian, while Favret dates from the Late Anisian, [14] between approximately 244 and 242 million years ago. [5]

The significant presence of marine reptiles, ammonites and other invertebrates in the Fossil Hill Member indicates that the surface waters were well aerated, [13] but there is little animal presence in the benthic zones, with the notable exception of bivalves of the family Halobiidae. The fossils found show that the stratigraphic unit was once a pelagic ecosystem with a stable food web. Bony fish are little known and have currently only been discovered in the Favret Formation. Among the fish discovered are the actinopterygians Saurichthys and an undetermined representative, [15] while among the sarcopterygians, numerous specimens of indeterminate coelacanthids are known. [5] The most abundant marine reptiles of the Fossil Hill Member are the ichthyosaurs, including Thalattoarchon itself, Phalarodon , Omphalosaurus and the large Cymbospondylus . Few other marine reptiles are known from the Fossil Hill Member, the only clearly identified being the sauropterygian Augustasaurus . [1] [4] [12] [5]

See also

Notes

  1. For an unclear reason, some sources list the year of discovery of the fossil specimen as 2010. [3]

Related Research Articles

<span class="mw-page-title-main">Ichthyosauria</span> Extinct order of large marine reptiles

Ichthyosauria is an order of large extinct marine reptiles sometimes referred to as "ichthyosaurs", although the term is also used for wider clades that the order resides in.

<i>Dinocephalosaurus</i> Extinct genus of reptiles

Dinocephalosaurus is a genus of long necked, aquatic protorosaur that inhabited the Triassic seas of China. The genus contains the type and only known species, D. orientalis, which was named by Chun Li in 2003. Unlike other long-necked protorosaurs, Dinocephalosaurus convergently evolved a long neck not through elongation of individual neck vertebrae, but through the addition of neck vertebrae that each had a moderate length. As indicated by phylogenetic analyses, it belonged in a separate lineage that also included at least its closest relative Pectodens, which was named the Dinocephalosauridae in 2021. Like tanystropheids, however, Dinocephalosaurus probably used its long neck to hunt, utilizing the fang-like teeth of its jaws to ensnare prey; proposals that it employed suction feeding have not been universally accepted. It was probably a marine animal by necessity, as suggested by the poorly-ossified and paddle-like limbs which would have prevented it from going ashore.

<i>Tanystropheus</i> Extinct genus of reptiles

Tanystropheus is an extinct genus of archosauromorph reptile which lived during the Triassic Period in Europe, Asia, and North America. It is recognisable by its extremely elongated neck, longer than the torso and tail combined. The neck was composed of 13 vertebrae strengthened by extensive cervical ribs. Tanystropheus is one of the most well-described non-archosauriform archosauromorphs, known from numerous fossils, including nearly complete skeletons. Some species within the genus may have reached a total length of 6 meters (20 ft), making Tanystropheus the longest non-archosauriform archosauromorph as well. Tanystropheus is the namesake of the family Tanystropheidae, a clade collecting many long-necked Triassic archosauromorphs previously described as "protorosaurs" or "prolacertiforms".

<i>Cymbospondylus</i> Extinct genus of reptiles

Cymbospondylus is an extinct genus of large ichthyosaurs, of which he is among the oldest representatives, that lived during the Anisian stage of the Middle Triassic in what are now North America and Europe. The first known fossils of this taxon are a set of more or less complete vertebrae which were discovered in the 19th century in various mountain ranges of Nevada, in the United States, before being named and described by Joseph Leidy in 1868. It is in the beginning of the 20th century that more complete fossils were discovered through several expeditions launched by the University of California, and described in more detail by John Campbell Merriam in 1908, thus visualizing the overall anatomy of the animal. While many species have been assigned to the genus, only five are recognized as valid, the others being considered synonymous, doubtful or belonging to other genera. Cymbospondylus was formerly classified as a representative of the Shastasauridae, but more recent studies consider it to be more basal, view as the type genus of the Cymbospondylidae.

<i>Mixosaurus</i> Extinct genus of reptiles

Mixosaurus is an extinct genus of Middle Triassic ichthyosaur. Its fossils have been found near the Italy–Switzerland border and in South China.

<i>Chaohusaurus</i> Extinct genus of reptiles

Chaohusaurus is an extinct genus of basal ichthyopterygian, depending on definition possibly ichthyosaur, from the Early Triassic of Chaohu and Yuanan, China.

<i>Himalayasaurus</i> Extinct genus of reptiles

Himalayasaurus is an extinct genus of ichthyosaur from the Late Triassic Qulonggongba Formation of Tibet. The type species Himalayasaurus tibetensis was described in 1972 on the basis of fragmentary remains, including teeth, limb bones, and vertebrae. The entire body length of Himalayasaurus is estimated to have been over 15 metres (49 ft) in length. Himalayasaurus has since been considered a nomen dubium or "dubious name" because of the lack of features that set it apart from other ichthyosaurs, although the presence of distinct cutting edges on its teeth have more recently been proposed as a unique feature of the genus. Himalayasaurus belongs to the family Shastasauridae, which includes other large-bodied Triassic ichthyosaurs like Shonisaurus.

<span class="mw-page-title-main">Thalattosauria</span> Extinct order of sea reptiles

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<i>Omphalosaurus</i> Extinct genus of reptiles

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<i>Augustasaurus</i> Extinct genus of reptiles

Augustasaurus is a genus of aquatic sauropterygian reptile belonging to the Pistosauria, a clade containing plesiosaurs and their close relatives. Pistosaurus and Augustasaurus were thought to be the only known members of the family Pistosauridae. However, some recent cladistic analyses found Augustasaurus to be a more advanced pistosaur, as a sister group of the order Plesiosauria. The only known species of Augustasaurus is Augustasaurus hagdorni, which was first described in 1997.

<i>Besanosaurus</i> Genus of Triassic ichthyosaur

Besanosaurus is a genus of Middle Triassic ichthyosaur from Monte San Giorgio of Italy and Switzerland, containing the single species B. leptorhynchus. Besanosaurus was named by Cristiano Dal Sasso and Giovanni Pinna in 1996, based on the nearly complete flattened skeleton BES SC 999, the holotype specimen. This skeleton is preserved across multiple thin rock slabs spanning 3.5 by 4 metres when assembled and took thousands of hours to prepare. Additional specimens from Monte San Giorgio that have previously been considered separate genera, including a partial skull named Mikadocephalus and a well-preserved, largely complete skeleton, have been reinterpreted as additional specimens of Besanosaurus.

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<i>Guizhouichthyosaurus</i> Extinct genus of reptiles

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<i>Toretocnemus</i> Extinct genus of reptiles

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Wimanius is a genus of ichthyosaur from the Middle Triassic of Switzerland, containing a single species, Wimanius odontopalatus. It was described by Michael Maisch and Andreas Matzke in 1998 based on an incomplete skull from Monte San Giorgio, a mountain on the Swiss-Italian border. Wimanius possesses teeth on its palate, though whether they were located on the palatine or pterygoid is disputed. Other features of Wimanius include a large orbit and jugals with two rami of similar lengths. Different phylogenetic placements of Wimanius have been recovered by different studies, including it being a mixosaurid relative or a merriamosaur, and a monotypic family, Wimaniidae has been named for it. However, its validity has also been questioned, and synonymy with various other genera has been proposed. The only specimen of Wimanius come from the Besano Formation. During the Anisian, this region was a lagoon populated by a wide variety of marine life, including a variety of other ichthyosaurs.

Mixosauridae was an early group of ichthyosaurs, living between 247.2 and 235 million years ago, during the Triassic period. Fossils of mixosaurs have been found all over the world: China, Timor, Indonesia, Italy, Germany, Spitsbergen, Switzerland, Svalbard, Canada, Alaska, and Nevada.

Guanlingsaurus is an extinct genus of shastasaurid ichthyosaur from the Late Triassic of China. It grew up to 8.3 metres (27 ft) in length and has a wide, triangular skull with a short and toothless snout.

Xinminosaurus is an extinct genus of cymbospondylid ichthyosaur known from the Middle Triassic of Guizhou Province, China.

<span class="mw-page-title-main">Timeline of ichthyosaur research</span>

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<i>Sclerocormus</i> Extinct genus of reptiles

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