Biology:Thalattoarchon
| Thalattoarchon | |
|---|---|
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| Holotype skull (FMNH PR 3032) | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Reptilia |
| Order: | †Ichthyosauria |
| Genus: | †Thalattoarchon Fröbisch et al., 2013 |
| Type species | |
| †Thalattoarchon saurophagis Fröbisch et al., 2013
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Thalattoarchon is an extinct genus of large predatory ichthyosaurs that lived during the Anisian stage of the Middle Triassic in what is now North America. The only known species is T. saurophagis, described in 2013 from a single specimen discovered in the Favret Formation, Nevada (United States ). 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.
As an ichthyosaur, Thalattoarchon had flippers for limbs and a fin on the tail. It is a large ichthyosaur, its size being estimated at 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.
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. 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 known 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][3][lower-alpha 1] after a period of work of three weeks. The recovered material where transported by an helicopter and a truck out of the field.[4] 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 swimming paddles.[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 and colleagues, 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.[4] The species 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][5]
Description
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][3][4] However, due to some missing parts of the only known specimen, the authors mentioned that the estimate could be revised when more is known about the animal.[1] In 2021, Sander and colleagues proposed that the animal would reach a body mass of 4.3 metric tons (4.7 short tons).[6] Like all other ichthyosaurs, Thalattoarchon has four flippers, but unlike the more derived 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 being estimated at 1.2 meters (3.9 ft) long.[5] The skull of Thalattoarchon is proportionally shorter but more robust than those of other ichthyosaurs.[7]
Skull
The skull of the only known 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 which 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.[5]
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.[5] 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 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.[5]
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.[5]
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 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, 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.[5]
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.[5][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.[8] This classification was generally accepted and retained in several phylogenetic analyses concerning ichthyosaurs published since.[9][10][11][12] In 2017, Benjamin C. Moon ran a variety of analyses, in which Thalattoarchon was recovered in a variety of positions, namely being more closely related to later ichthyosaurs, earlier-branching than Cymbospondylus, or the sister taxon of C. nichollsi.[10] In 2021, Paul Martin Sander and his colleagues reclassified Thalattoarchon within the Merriamosauria, but this time as the sister taxon of the Shastasauridae.[2][6]
The following cladogram shows the position of Thalattoarchon within the Ichthyosauromorpha after Sander et al. (2021):[2][6]
| Ichthyosauromorpha |
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Paleobiology
Due to its bicarinate, cuting 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][3][4][7] 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.[5]
Palaeoecology
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 m wide.[14][6] 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.[6]
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 Halobiidae family. The fossils found show that the rock 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.[6] 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][5][2][6]
See also
- List of ichthyosaurs
- Timeline of ichthyosaur research
Notes
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 Nadia B. Fröbisch; Jörg Fröbisch; P. Martin Sander; Lars Schmitz; Olivier Rieppel (2013). "Macropredatory ichthyosaur from the Middle Triassic and the origin of modern trophic networks". Proceedings of the National Academy of Sciences of the United States of America 110 (4): 1393–1397. doi:10.1073/pnas.1216750110. PMID 23297200. Bibcode: 2013PNAS..110.1393F.
- ↑ 2.0 2.1 2.2 2.3 P. Martin Sander; Eva Maria Griebeler; Nicole Klein; Jorge Velez Juarbe; Tanja Wintrich; Liam J. Revell; Lars Schmitz (2021). "Early giant reveals faster evolution of large body size in ichthyosaurs than in cetaceans". Science 374 (6575): eabf5787. doi:10.1126/science.abf5787. PMID 34941418.
- ↑ 3.0 3.1 3.2 Riley Black (January 7, 2013). "Sharp-Toothed Thalattoarchon Was the First Ruler of the Triassic Seas". https://www.nationalgeographic.com/science/article/sharp-toothed-thalattoarchon-was-the-first-ruler-of-the-triassic-seas.
- ↑ 4.0 4.1 4.2 4.3 4.4 Field Museum (January 7, 2013). "Giant fossil predator provides insights into the rise of modern marine ecosystem structures". https://www.sciencedaily.com/releases/2013/01/130107151422.htm.
- ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 5.8 5.9 Nadia B. Fröbisch; Jörg Fröbisch; P. Martin Sander; Lars Schmitz; Olivier Rieppel (2013). "Supporting Information". Proceedings of the National Academy of Sciences of the United States of America. doi:10.1073/pnas.1216750110. https://www.pnas.org/action/downloadSupplement?doi=10.1073%2Fpnas.1216750110&file=pnas.201216750si.pdf.
- ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 P. Martin Sander; Eva Maria Griebeler; Lars Schmitz (2021). "Supplementary Materials for Early giant reveals faster evolution of large body size in ichthyosaurs than in cetaceans". Science. doi:10.1126/science.abf5787. https://www.science.org/action/downloadSupplement?doi=10.1126%2Fscience.abf5787&file=science.abf5787_sm.pdf.
- ↑ 7.0 7.1 Ryan Marek (2015). "Fossil Focus: Ichthyosaurs". Palaeontology Online 5: 8. https://www.palaeontologyonline.com/articles/2015/fossil-focus-ichthyosaurs/. Retrieved 13 June 2020.
- ↑ Cheng Ji; Da-Yong Jiang; Ryosuke Motani; Olivier Rieppel; Wei-Cheng Hao; Zuo-Yu Sun (2017). "Phylogeny of the Ichthyopterygia incorporating recent discoveries from South China". Journal of Vertebrate Paleontology 36 (1): e1025956. doi:10.1080/02724634.2015.1025956. https://www.researchgate.net/publication/283840343.
- ↑ Da-Yong Jiang; Ryosuke Motani; Jian-Dong Huang; Andrea Tintori; Yuan-Chao Hu; Olivier Rieppel; Nicholas C. Fraser; Cheng Ji et al. (2016). "A large aberrant stem ichthyosauriform indicating early rise and demise of ichthyosauromorphs in the wake of the end-Permian extinction". Scientific Reports 6: 26232. doi:10.1038/srep26232. PMID 27211319. Bibcode: 2016NatSR...626232J.
- ↑ 10.0 10.1 Benjamin C. Moon (2017). "A new phylogeny of ichthyosaurs (Reptilia: Diapsida)". Journal of Systematic Palaeontology 17 (2): 129–155. doi:10.1080/14772019.2017.1394922. https://research-information.bris.ac.uk/ws/portalfiles/portal/142491822/Typescript_A_new_phylogeny_of_ichthyosaurs.pdf.
- ↑ Jian-dong Huang; Ryosuke Motani; Da-yong Jiang; Xin-xin Ren; Andrea Tintori; Olivier Rieppel; Min Zhou; Yuan-chao Hu et al. (2020). "Repeated evolution of durophagy during ichthyosaur radiation after mass extinction indicated by hidden dentition". Scientific Reports 10 (1): 7798. doi:10.1038/s41598-020-64854-z. PMID 32385319. Bibcode: 2020NatSR..10.7798H.
- ↑ Gabriele Bindellini; Andrzej S. Wolniewicz; Feiko Miedema; Torsten M. Scheyer; Cristiano Dal Sasso (2021). "Cranial anatomy of Besanosaurus leptorhynchus Dal Sasso & Pinna, 1996 (Reptilia: Ichthyosauria) from the Middle Triassic Besano Formation of Monte San Giorgio, Italy/Switzerland: taxonomic and palaeobiological implications". PeerJ 9: e11179. doi:10.7717/peerj.11179. PMID 33996277.
- ↑ 13.0 13.1 Kathryn M. Nichols; Norman J. Silberling (1977). Stratigraphy and depositional history of the Star Peak Group (Triassic), northwestern Nevada. 175-178. Boulder: Geological Society of America, Special Papers. pp. 73. doi:10.1130/SPE178-p1. ISBN 978-0-813-72178-1. https://books.google.com/books?id=ojSgyTAPuJgC.
- ↑ 14.0 14.1 Nicole Klein; Lars Schmitz; Tanja Wintrich; P. Martin Sander (2020). "A new cymbospondylid ichthyosaur (Ichthyosauria) from the Middle Triassic (Anisian) of the Augusta Mountains, Nevada, USA". Journal of Systematic Palaeontology 18 (14): 1167–1191. doi:10.1080/14772019.2020.1748132. https://www.researchgate.net/publication/340802048.
- ↑ P. Martin Sander; Olivier C. Rieppel; H. Bucher (1994). "New Marine Vertebrate Fauna from the Middle Triassic of Nevada". Journal of Paleontology 68 (3): 676–680. doi:10.1017/S0022336000026020.
External links
Wikidata ☰ Q2756895 entry
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