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Tenontosaurus

Tenontosaurus (/tɪˌnɒntəˈsɔːrəs/ ti-NON-tə-SOR-əs; lit. 'sinew lizard') is a genus of iguanodontian ornithopod dinosaur. It had an unusually long, broad tail, which like its back was stiffened with a network of bony tendons.

Tenontosaurus
Temporal range: Early Cretaceous (Aptian to Albian), 115–108 Ma
T. dossi on exhibit in the Perot Museum of Nature and Science
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: †Ornithischia
Clade: †Neornithischia
Clade: †Ornithopoda
Clade: †Tenontosauridae
Genus: †Tenontosaurus
Ostrom, 1970
Species
  • †T. tilletti Ostrom, 1970 (type)
  • †T. dossi Winkler, Murry & Jacobs, 1997

The genus is known from the late Aptian to Albian ages of the Early Cretaceous period sediments of western North America, dating between 115 and 108 million years ago. It contains two species, Tenontosaurus tilletti (described by John Ostrom in 1970[1]) and Tenontosaurus dossi (described by Winkler, Murry, and Jacobs in 1997).[2] Many specimens of T. tilletti have been collected from several geological formations throughout western North America. T. dossi is known from only a handful of specimens collected from the Twin Mountains Formation of Parker County, Texas.

History of discovery

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Restoration of T. tilletti
 
Tenontosaurus tilletti (red) compared in size to a human and other ornithopods

The first Tenontosaurus fossil was found in Big Horn County, Montana by an American Museum of Natural History (AMNH) expedition in 1903. Subsequent digs in the same area during the 1930s unearthed 18 more specimens, and four specimens were found during the 1940s. Despite the large number of fossil specimens, the animal was not named or scientifically described during this time, though Barnum Brown of the AMNH gave it the informal name "Tenantosaurus", "sinew lizard", in reference to the extensive system of stiffening tendons in its back and tail.[3]

During the 1960s, Yale University began an extensive, long-term dig in the Big Horn Basin area (Cloverly Formation) of Montana and Wyoming. The expedition was led by John Ostrom, whose team discovered more than 40 new specimens. Following his expedition, Ostrom became the first to describe and name the animal, calling it Tenontosaurus,[4] a slight variation in spelling of Brown's informal name.

Since 1970, many more Tenontosaurus specimens have been reported, both from the Cloverly and other geological formations, including the Antlers Formation in Oklahoma, Paluxy Formation of Texas, Wayan Formation of Idaho, Cedar Mountain Formation of Utah, and Arundel Formation of Maryland.[3]

Description

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Tenontosaurus was a medium-sized ornithopod, with both species weighing about 1,000 kilograms (2,200 lb). Paul in 2016 estimated that T. tilletti would have been 6 metres (20 ft) and weighed 600 kilograms (1,300 lb),[5] but Campione and Evans in 2020 estimated that this species would have weighed up to 971–1,019 kilograms (2,141–2,247 lb).[6] Paul also estimated that T. dossi would have been 7 meters (23 ft) long and weighed 1,000 kilograms (2,200 lb).[5] Adult length estimates among other researchers range between 7 and 8 metres (23 and 26 ft).[2][7]

Tenontosaurus was a facultative quadruped, capable of assuming either a bipedal or quadrupedal stance. It may have used a quadrupedal stance while feeding,[4][8] but was probably incapable of rapid quadrupedal movement.[4] Tenontosaurus resembles quadrupedal ornithischians in having a tibia that is shorter than the femur and an anterolateral process on the ulna, but it resembles bipedal ornithischians in having a relatively narrow pelvis and a pendant fourth trochanter.[8] The manus (the hand/front foot) shows a mixture of traits associated with bipeds and quadrupeds. It retains narrow claws, unlike the hoof-like unguals of quadrupedal ornithischians,[8][9] has a short metacarpus, as in the bipedal Hypsilophodon, and retains grasping adaptations. However, the phalanges are also shortened as an adaptation to weight bearing.[9] An analysis of the overall proportions and center of mass of Tenontosaurus found it to be a quadruped, although the analysis only distinguished bipeds from quadrupeds without including a facultatively bipedal category.[10]

Classification

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Front part of skeleton

Tenontosaurus was originally classified in the family Iguanodontidae,[1] although subsequent authors challenged this classification and proposed it actually belonged to Hypsilophodontidae.[3] Subsequent phylogenetic analyses have found Tenontosaurus to be intermediate in position between Hypsilophodon-like taxa and Iguanodon-like taxa, as a non-dryomorph iguanodont. The precise phylogenetic position of Tenontosaurus varies between studies, with some studies finding it to be more closely related to dryomorphs than rhabdodontids, some studies finding it to be the sister taxon of a clade uniting rhabdodontids and dryomorphs, and some studies finding it to be closely related to rhabdodontids. The discovery of Iani in 2023 lent support for a close relationship between Tenontosaurus and rhabdodontids, as Iani exhibits transitional characteristics between Tenontosaurus and other rhabdodontomorphs.[11]

The cladogram below follows an analysis by Butler et al, 2011.[12]

Ornithopoda

Paleobiology

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Diet

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Plant life in the Tenontosaurus ecosystem was likely dominated by ferns and tree ferns, cycads, and possibly primitive flowering plants. Larger plants and trees were represented by gymnosperms, such as conifer and ginkgo trees. Tenontosaurus was a low browser, and an adult would have had a maximum browsing height of about 3 meters (10 ft) if it adopted a bipedal stance. This restricted Tenontosaurus, especially juveniles, to eating low-growing ferns and shrubs. Its powerful, U-shaped beak and the angled cutting surfaces of its teeth, however, meant it was not limited to which part of the plant it consumed. Leaves, wood, and even fruit may have formed part of its diet.[3]

Predators

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T. tilletti with juveniles, in front of Deinonychus

Teeth and a number of skeletons belonging to the carnivorous theropod Deinonychus have often been discovered associated with Tenontosaurus tilletti remains. Tenontosaurus specimens have been found at over 50 sites, and 14 of those also contain Deinonychus remains. According to one 1995 study, only six sites containing Deinonychus fossils contain no trace of Tenontosaurus, and Deinonychus remains are only rarely found associated with other potential prey, like Sauropelta.[13] In all, 20% of Tenontosaurus fossils are found in close proximity to Deinonychus, and several scientists have suggested that this implies Deinonychus was the major predator of Tenontosaurus. Adult Deinonychus, however, were much smaller than adult Tenontosaurus, and it is unlikely a single Deinonychus would have been capable of attacking a fully grown Tenontosaurus. While some scientists have suggested that Deinonychus must therefore have been a pack hunter, this view has been challenged based on both a supposed lack of evidence for coordinated hunting (rather than mobbing behavior as in most modern birds and reptiles, though crocodilians have been documented to hunt cooperatively on occasion[14]) as well as evidence that Deinonychus may have been cannibalizing each other, as well as the Tenontosaurus, in a feeding frenzy.[15] It is likely that Deinonychus favored juvenile Tenontosaurus, and that when Tenontosaurus reached a certain size, it passed out of range as a food source for the small theropods, though they may have scavenged larger individuals, or preyed on adults that were sick or injured. The fact that most Tenontosaurus remains found with Deinonychus are half-grown individuals supports this view.[3][16] It also lived in the same area as the large carnivorous dinosaur Acrocanthosaurus.[17]

Reproduction

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Osteohistology of the diaphyseal femur of two juveniles

The presence of medullary bone tissue in the thigh bone and shin bone of one specimen indicates that Tenontosaurus used this tissue, today only found in birds that are laying eggs, in reproduction. Additionally, like Tyrannosaurus and Allosaurus, two other dinosaurs known to have produced medullary bone, the tenontosaur individual was not at full adult size upon her death at 8 years old. Because the theropod line of dinosaurs that includes Allosaurus and Tyrannosaurus diverged from the line that led to Tenontosaurus very early in the evolution of dinosaurs, this suggests that dinosaurs in general produced medullary tissue and reached reproductive maturity before maximum size.[18] A histological study showed that T. tilletti grew quickly early in life and during sub-adult ontogeny, but grew very slowly in the years approaching maturity, unlike other iguanodontians.[19]

Paleoecology

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Complete fossil

Throughout the Cloverly Formation, Tenontosaurus is by far the most common vertebrate, five times more abundant than the next most common, the ankylosaur Sauropelta.[20] In the arid Little Sheep Mudstone Member, Tenontosaurus is the only herbivorous dinosaur, and it shared its environment with the common predator Deinonychus as well as an indeterminate species of allosauroid theropod and goniopholid crocodile. After the major climate shift at the beginning of the Himes Member in the mid-Albian age, several more dinosaurs entered the region, including the less common ornithopod Zephyrosaurus, the oviraptorosaur Microvenator, and an indeterminate species of titanosauriform sauropod and ornithomimid. The ecological community in the tropical stage also included the small mammal Gobiconodon, turtles such as Glyptops, and species of lungfish.[3]

 
Mounted skeletons of an adult with juveniles

The ecological community was similar in other regions, with dinosaurs like Tenontosaurus and Deinonychus as the most common large vertebrates. The Antlers Formation stretches from southwest Arkansas through southeastern Oklahoma and into northeastern Texas. This geological formation has not been dated radiometrically. Scientists have used biostratigraphic data and the fact that it shares several of the same genera as the Trinity Group of Texas, to surmise that this formation was laid down during the Albian stage of the Early Cretaceous Period, approximately 110 mya.[21] The area preserved in this formation was a large floodplain that drained into a shallow inland sea. Several million years later, this sea would expand to the north, becoming the Western Interior Seaway and dividing North America in two for nearly the entire Late Cretaceous period. The paleoenvironment of the Antlers Formation consisted of tropical or sub-tropical forests, floodplains, river deltas, coastal swamps, bayous and lagoons, probably similar to that of modern-day Louisiana.[21][3] In the Antlers Formation in what is now Oklahoma, Tenontosaurus and Deinonychus shared their paleoenvironment with other dinosaurs, such as the sauropods Astrodon (Pleurocoelus) and Sauroposeidon proteles, and the carnosaur Acrocanthosaurus atokensis, which was likely the apex predator in this region.[22][16] The most common dinosaur in the paleoenvironment preserved in this formation is Tenontosaurus. Other vertebrates present at the time of Tenontosaurus included the amphibian Albanerpeton arthridion, the reptiles Atokasaurus metarsiodon and Ptilotodon wilsoni, the crurotarsan reptile Bernissartia, the cartilaginous fish Hybodus buderi and Lissodus anitae, the ray-finned fish Gyronchus dumblei, the crocodilian Goniopholis, and the turtles Glyptops and Naomichelys.[23][24] Possible indeterminate bird remains are also known from the Antlers Formation. The fossil evidence suggests that the gar Lepisosteus was the most common vertebrate in this region. The early mammals known from this region include Atokatherium boreni and Paracimexomys crossi.[25]

Climate

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In the Cloverly Formation of Montana and Wyoming, Tenontosaurus remains are common in two distinct rock units: the more ancient Little Sheep Mudstone Member (Cloverly Formation unit V) and the more recent Himes Member (units VI and VII). The oldest part of the formation, the Pryor Conglomerate, contains no Tenontosaurus fossils, and they only appear in the uppermost, most recent part of the Little Sheep Mudstone Member. Catherine Forster, in a 1984 paper on the ecology of Tenontosaurus, used this as evidence to suggest that Tenontosaurus populations did not arrive in the Bighorn Basin area until the time of the late Little Sheep Mudstone Member.[3]

At the time Tenontosaurus first appeared in Wyoming and Montana (the early Albian age), the regions climate was arid to semi-arid, dry, with seasonal periods of rainfall and occasional droughts. However, during a period of a few million years, the climate in the region shifted to one of increased rainfall, and the environment became subtropical to tropical, with river deltas, floodplains, and forests with swampy inlets reminiscent of modern Louisiana, though marked dry seasons persisted to create savannah-like environments as well.[21] The change in rainfall levels is likely due to the advancing shoreline of the Skull Creek Seaway, a cycle of the Western Interior Seaway which, later in the Cretaceous period, would completely divide North America.[3]

This dramatic shift in climate coincided with an apparent increase, rather than decrease, in the abundance of Tenontosaurus. This shows Tenontosaurus to have been a remarkably adaptable animal, which persisted for a long span of time in one area despite changes to its environment.[3]

References

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  1. ^ a b Ostrom, J. H. (1970). "Stratigraphy and paleontology of the Cloverly Formation (Lower Cretaceous) of the Bighorn Basin area, Wyoming and Montana". Bulletin of the Peabody Museum of Natural History. 35: 1–234. ISSN 0079-032X.
  2. ^ a b Winkler, Dale A.; Murry, Phillip A.; Jacobs, Louis L. (1997). "A new species of Tenontosaurus (Dinosauria: Ornithopoda) from the Early Cretaceous of Texas". Journal of Vertebrate Paleontology. 17 (2): 330–348. Bibcode:1997JVPal..17..330W. doi:10.1080/02724634.1997.10010978. JSTOR 4523810.
  3. ^ a b c d e f g h i j Forster, C. A. (1984). "The paleoecology of the ornithopod dinosaur Tenontosaurus tilletti from the Cloverly Formation, Big Horn Basin of Wyoming and Montana". The Mosasaur. 2: 151–163.
  4. ^ a b c Forster, Catherine A. (1990). "The postcranial skeleton of the ornithopod dinosaur Tenontosaurus tilletti". Journal of Vertebrate Paleontology. 10 (3): 273–294. Bibcode:1990JVPal..10..273F. doi:10.1080/02724634.1990.10011815. ISSN 0272-4634. JSTOR 4523326.
  5. ^ a b Paul, Gregory S. (2016). The Princeton Field Guide to Dinosaurs. Princeton University Press. p. 311. ISBN 978-1-78684-190-2. OCLC 985402380.
  6. ^ Campione, N. E.; Evans, D. C. (2020). "The accuracy and precision of body mass estimation in non-avian dinosaurs". Biological Reviews. 95 (6): 1759–1797. doi:10.1111/brv.12638. PMID 32869488. S2CID 221404013. Supporting Information
  7. ^ Butler, R.J.; Barrett, P.M. (2012). "26. Ornithopods". In Brett-Surman, M.K.; Holtz, T.R.; Farlow, J.O. (eds.). The Complete Dinosaur (Life of the Past). Indiana University Press. p. 647. ISBN 978-0253357014.
  8. ^ a b c Maidment, Susannah; Barrett, Paul (2012-09-21). "Osteological correlates for quadrupedality in ornithischian dinosaurs". Acta Palaeontologica Polonica. 59 (1): 53–70. doi:10.4202/app.2012.0065. ISSN 0567-7920.
  9. ^ a b Hunt, Tyler C.; Cifelli, Richard L.; Davies, Kyle L. (2021-07-16). "The hand of Tenontosaurus tilletti (Dinosauria, Ornithopoda)". Journal of Vertebrate Paleontology. 41 (2). Bibcode:2021JVPal..41E8591H. doi:10.1080/02724634.2021.1938591. ISSN 0272-4634.
  10. ^ Bishop, Peter J.; Bates, Karl T.; Allen, Vivian R.; Henderson, Donald M.; Randau, Marcela; Hutchinson, John R. (2020-10-16). "Relationships of mass properties and body proportions to locomotor habit in terrestrial Archosauria". Paleobiology. 46 (4): 550–568. Bibcode:2020Pbio...46..550B. doi:10.1017/pab.2020.47. eISSN 1938-5331. ISSN 0094-8373.
  11. ^ Zanno, Lindsay E.; Gates, Terry A.; Avrahami, Haviv M.; Tucker, Ryan T.; Makovicky, Peter J. (2023-06-07). "An early-diverging iguanodontian (Dinosauria: Rhabdodontomorpha) from the Late Cretaceous of North America". PLOS ONE. 18 (6): –0286042. Bibcode:2023PLoSO..1886042Z. doi:10.1371/journal.pone.0286042. ISSN 1932-6203. PMC 10246810. PMID 37285376.
  12. ^ Richard J. Butler, Jin Liyong, Chen Jun, Pascal Godefroit (2011). "The postcranial osteology and phylogenetic position of the small ornithischian dinosaur Changchunsaurus parvus from the Quantou Formation (Cretaceous: Aptian–Cenomanian) of Jilin Province, north-eastern China". Palaeontology. 54 (3): 667–683. Bibcode:2011Palgy..54..667B. doi:10.1111/j.1475-4983.2011.01046.x.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. ^ Maxwell, W. D.; Ostrom, J. H. (1995). "Taphonomy and paleobiological implications of Tenontosaurus-Deinonychus associations". Journal of Vertebrate Paleontology. 15 (4): 707–712. Bibcode:1995JVPal..15..707M. doi:10.1080/02724634.1995.10011256. (abstract Archived 2007-09-27 at the Wayback Machine)
  14. ^ Dinets, Vladimir (2015). "Apparent coordination and collaboration in cooperatively hunting crocodilians". Ethology Ecology & Evolution. 27 (2): 244–250. Bibcode:2015EtEcE..27..244D. doi:10.1080/03949370.2014.915432. S2CID 84672219.
  15. ^ Roach, B. T.; Brinkman, D. L. (2007). "A reevaluation of cooperative pack hunting and gregariousness in Deinonychus antirrhopus and other nonavian theropod dinosaurs". Bulletin of the Peabody Museum of Natural History. 48 (1): 103–138. doi:10.3374/0079-032X(2007)48[103:AROCPH]2.0.CO;2. S2CID 84175628.
  16. ^ a b Brinkman, Daniel L.; Cifelli, Richard L.; Czaplewski, Nicholas J. (1998). "First Occurrence of Deinonychus antirrhopus (Dinosauria: Theropoda) from the Antlers Formation (Lower Cretaceous: Aptain-Albian) of Oklahoma". Oklahoma Geological Survey (164): 1–27.
  17. ^ D'Emic, Michael D.; Melstrom, Keegan M.; Eddy, Drew R. (2012). "Paleobiology and geographic range of the large-bodied Cretaceous theropod dinosaur Acrocanthosaurus atokensis". Palaeogeography, Palaeoclimatology, Palaeoecology. 333–334: 13–23. Bibcode:2012PPP...333...13D. doi:10.1016/j.palaeo.2012.03.003.
  18. ^ Lee, Andrew H.; Werning, Sarah (2008). "Sexual maturity in growing dinosaurs does not fit reptilian growth models". Proceedings of the National Academy of Sciences. 105 (2): 582–587. Bibcode:2008PNAS..105..582L. doi:10.1073/pnas.0708903105. PMC 2206579. PMID 18195356.
  19. ^ Werning, S. (2012). "The Ontogenetic osteohistology of Tenontosaurus tilletti". PLOS ONE. 7 (3): e33539. Bibcode:2012PLoSO...733539W. doi:10.1371/journal.pone.0033539. PMC 3314665. PMID 22470454.
  20. ^ Oreska, Matthew P. J.; Carrano, Matthew T.; Dzikiewicz, Katherine M. (March 2013). "Vertebrate paleontology of the Cloverly Formation (Lower Cretaceous), I: faunal composition, biogeographic relationships, and sampling". Journal of Vertebrate Paleontology. 33 (2): 264–292. Bibcode:2013JVPal..33..264O. doi:10.1080/02724634.2012.717567. ISSN 0272-4634. S2CID 83674985.
  21. ^ a b c Wedel, M. J.; Cifelli, R. L. (2005). "Sauroposeidon: Oklahoma's Native Giant" (PDF). Oklahoma Geology Notes. 65 (2): 40–57. Archived from the original (PDF) on 2008-07-05. Retrieved 2007-07-07.
  22. ^ Weishampel, David B.; Barrett, Paul M.; Coria, Rodolfo A.; Le Loeuff, Jean; Xu Xing; Zhao Xijin; Sahni, Ashok; Gomani, Elizabeth, M.P.; and Noto, Christopher R. (2004). "Dinosaur Distribution", in The Dinosauria (2nd), p. 264.
  23. ^ Nydam, Randall L.; Cifelli, Richard L. (2002-07-08). "Lizards from the Lower Cretaceous (Aptian–Albian) Antlers and Cloverly Formations". Journal of Vertebrate Paleontology. 22 (2): 286–298. doi:10.1671/0272-4634(2002)022[0286:LFTLCA]2.0.CO;2. eISSN 1937-2809. ISSN 0272-4634.
  24. ^ Cifelli, Richard L.; Gardner, James D.; Nydam, Randall L.; Brinkman, Daniel L. (August 1997). "Additions to the vertebrate fauna of the Antlers Formation (Lower Cretaceous), southeastern Oklahoma". Oklahoma Geology Notes. 57 (4): 124–131.
  25. ^ Kielan-Jaworowska, Zofia; Cifelli, Richard L (2001). "Primitive boreosphenidan mammal (?Deltatheroida) from the Early Cretaceous of Oklahoma". Acta Palaeontologica Polonica. 46 (3): 377–391. ISSN 0567-7920.
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