Postosuchus

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Postosuchus
Temporal range: Late Triassic (Norian)
Postosuchus.jpg
Skeleton at the Museum of Texas Tech University, near Post, Texas
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Archosauria
Clade: Pseudosuchia
Family:† Rauisuchidae
Genus:† Postosuchus
Chatterjee, 1985
Type species
†Postosuchus kirkpatricki
Chatterjee, 1985
Species
  • †P. kirkpatrickiChatterjee, 1985
  • †P. alisonaePeyer et al., 2008

Postosuchus, meaning "Crocodile from Post", is an extinct genus of rauisuchid reptiles comprising two species, P. kirkpatricki and P. alisonae, that lived in what is now North America during the Late Triassic. Postosuchus is a member of the clade Pseudosuchia, the lineage of archosaurs that includes modern crocodilians (the other main group of archosaurs is Avemetatarsalia, the lineage that includes all archosaurs more closely related to birds than to crocodilians). Its name refers to Post Quarry, a place in Texas where many fossils of the type species, P. kirkpatricki, were found. It was one of the apex predators of its area during the Triassic, larger than the small dinosaur predators of its time (such as Coelophysis ). It was a hunter which probably preyed on large bulky herbivores like dicynodonts and many other creatures smaller than itself (such as early dinosaurs). [1]

Contents

The skeleton of Postosuchus is large and robust with a deep skull and a long tail. It was a large animal up to 5–6 m (16–20 ft) long or even more. [2] [3] The extreme shortness of the forelimbs relative to the hind limbs, the very small hands, and measurements of the vertebrae suggest that Postosuchus may have been committed to bipedal locomotion. [3]

Description

P. kirkpatricki compared to a human Postosuchus kirkpatricki.jpg
P. kirkpatricki compared to a human

Postosuchus was one of the largest carnivorous reptiles during the late Triassic. The length of the paratype is estimated up to 3.5–4 m (11–13 ft) long, [3] and an individual of such length would have measured 2 metres (6.6 ft) tall at the head when stood upright and weighed around 250–300 kilograms (550–660 lb). [4] The holotype is estimated up to 5–6 m (16–20 ft) long, and the largest known individual may measure up to 5–7 m (16–23 ft) long or more based on a complete cervical series specimen (TTU-P 9235). [3] [5]

The neck of Postosuchus consists of at least eight cervical vertebrae followed by sixteen dorsals, while four co-ossified sacral vertebrae supported the hips. The neck was elongated, expanding to a short torso and long tail. Along with remains of the skeleton, paleontologists also identify osteoderms, which were thick plates forming scales on its back, neck, and possibly above or under the tail. [4] It is thought to have had over thirty vertebrae in the tail decreasing in size to the end. The pelvis with the hooked pubis and the rod-like ischium looked like those of carnosaurs. The ribcage of Postosuchus had typical archosaur structure, composed of large and slender, curved ribs. [4] In some discoveries ribs were found associated with gastralia, dermal bones located in the ventral region of the body. [6]

Skull

Skull cast Postosuchus profile.jpg
Skull cast
A tooth belonging to Postosuchus from the Upper Triassic Chinle Formation. Postosuchus tooth from Arizona.jpg
A tooth belonging to Postosuchus from the Upper Triassic Chinle Formation.

Postosuchus had a massively built skull, bearing dagger-like teeth, which was constructed narrow in front, and extended wide and deep behind. The holotype skull was 55 cm in length and 21 cm broad and deep. There are many fenestrae (openings) present in the bones that lighten the skull, providing space for the muscles. Like more derived archosaurs, the lower jaw had mandibular fenestrae (openings at the lower jaw), formed by the junction of the dentary with other jaw bones (surangular and angular). [4]

Postosuchus likely had very good long distant sight, due to large orbits, supporting large and sharp eyes, and strong olfaction provided by elongated nostrils. Inside the skull, under the nostrils, there was a hollow that may have contained the Jacobson's organ, an olfactory sensory organ sometimes referred as the "sixth sense". The jaws held large and sharp serrated teeth, of which some were developed even larger to operate as hooked sabers. [4]

A complete tooth found among Postosuchus remains in North Carolina measured about 7.2 cm in height. [7] Postosuchus possessed heterodonty dentition, which means each tooth was different in size and shape from the others. The upper jaw contained seventeen teeth, with each premaxilla bearing only four teeth and each maxilla thirteen teeth. [4] In the lower jaw were over thirty teeth. Replacement activity in Postosuchus was different from that of crocodiles, since the replacement tooth didn't fit directly in the pulp cavity of the old tooth, but grew until resorption of the old tooth was complete. [4]

Limbs and posture

With the forelimbs being approximately 64% the size of the hindlimbs, Postosuchus had small hands bearing five toes, of which only the first digit bore a claw. Due to the diminutive size of the hands, it is uncertain this claw was especially predominant in predation, but it may have helped in grappling prey. [8] The feet were much larger than the hands, with the fifth metatarsal forming a hook shape. The innermost two digits were less robust than the other toes, and likely could not touch the ground. [4] As it was a crurotarsan, the heel and ankle of Postosuchus resemble those of modern crocodiles.

Restoration showing quadrupedal pose Postosuchus BW.jpg
Restoration showing quadrupedal pose

The limbs were located underneath the body giving Postosuchus an upright stance. [4] Historically, there has been debate over whether or not rauisuchids like Postosuchus were mainly bipedal or quadrupedal. Each one of Postosuchus's two forelimbs was slightly over half the size of the hindlimbs. [4] This characteristic of short forelimbs can usually be seen in bipedal reptiles. Chatterjee suggested that Postosuchus could walk in an erect stance, since the short forelimbs were probably used only during slow locomotion. [4] In 1995 Robert Long and Phillip A. Murry argued that Postosuchus was heavily built and quadrupedal. [9] Peyer et al. 2008, argued that the thick pectoral girdle served for locomotion of the forelimbs. [8] They noted that this does not, however, detract from the theory that Postosuchus could also walk bipedally. [8] In 2013, a major study of the skeletal structure concluded that Postosuchus may have been an obligate biped based on evidence from the anatomy of the digits, vertebrae, and pelvis. The proportions of the limbs and weight-bearing sections of the spine were very similar to many theropod dinosaurs, nearly all of which are thought to have been strictly bipedal. [3] However a 2015 study noted several load-bearing adaptations present in the manus of Postosuchus, substantiating the view that its manus was used for support. [10] In a 2022 article Postosuchus was considered predominantly bipedal, but probably still capable of supporting its weight on the forelimbs at low speeds, and an ontogenetic shift was noted, with the shortening of the arms as individuals aged, suggesting that at least hatchlings and juveniles were facultatively quadrupedal. [11]

History

Postosuchus have been discovered only in the United States within the states of Arizona, New Mexico, North Carolina and Texas. Postosuchus Map Discoveries.png
Postosuchus have been discovered only in the United States within the states of Arizona, New Mexico, North Carolina and Texas.

During an expedition in 1980, paleontologists of the Texas Tech University discovered a new geological site rich in fossils near Post, Garza County, Texas, US, where a dozen well-preserved specimens belonging to a new rauisuchid were found. [4] In the following years further excavation in the Post Quarry, in Cooper Canyon Formation (Dockum Group), unearthed many remains of late Triassic terrestrial fauna. The holotype of P. kirkpatricki (TTUP 9000), representing a well-preserved skull and a partial postcranial skeleton, was described along with other findings of this new genus by paleontologist Sankar Chatterjee in 1985. A paratype, TTU-P 9002, representing a well-preserved skull and a complete skeleton was also assigned to this species. Chatterjee named the species after Mr. and Mrs. Jack Kirkpatrick who helped during his fieldwork. [12] Subsequently, some specimens (such manus and toe bones) were re-assigned to Chatterjeea and Lythrosuchus ; [13] Long and Murry pointed out that many of the juvenile skeletons (TTUP 9003-9011), which Chatterjee assigned to P. kirkpatricki, belong to a distinct genus, named Chatterjeea elegans. [14] Furthermore, in 2006 Nesbitt and Norell argued that Chatterjeea is a junior synonym of Shuvosaurus . [15]

In 2008, Peyer et al., described a new species of Postosuchus, P. alisonae that was discovered by two UNC undergrad students, Brian Coffey and Marco Brewer in 1992 in Triangle Brick Co. Quarry, Durham County, North Carolina. [16] The remains were prepared and reconstructed between 1994 and 1998 by the Department of Geological Sciences at the University of North Carolina. [17] The specific name is in reference to Alison L. Chambers, who worked to popularize paleontology in North Carolina. [16] The skeleton of P. alisonae consists of a few cranial bones, seven neck, one back, and four tail vertebrae, ribs, gastralia ("belly ribs"), chevrons, bony scutes, much of the shoulder girdles, most of the forelimbs except the left wrist and hand, most of the hindlimbs except for the thigh bones, and pieces from the hip. [18] Moreover, the well-preserved remains of P. alisonae shed new light on parts of Postosuchus anatomy, which were previously not well known. Specifically, the differences between the manus bones of P. kirkpatricki and P. alisonae confirm the chimera theory (associated fossils belonging to different animals) suggested by Long and Murry. [18] [13] The holotype specimen of P. alisonae (UNC 15575) is also unusual in its preservation of gut contents: bones from at least four other animals, including a partial skeleton of an aetosaur, a snout, coracoid, and humerus of the traversodontid cynodont Plinthogomphodon , two phalanges from a dicynodont, and a possible temnospondyl bone. [17] Furthermore, the Postosuchus was positioned on top of a skeleton of the sphenosuchian Dromicosuchus , which included tooth marks on the skull and neck. [17] P. alisonae represents the largest suchian reptile recovered from the quarry and the first articulated specimen of 'rauisuchian' archosaur found in eastern North America. [17]

Putative occurrences

Specimens similar to Postosuchus were discovered in Crosby County, Texas in 1920, and described by paleontologist Ermine Cowles Case in 1922. [19] [20] The fossils were composed only of an isolated braincase (UM 7473) and fragments of pelvic bones (UM 7244). Case then mistakenly assigned these specimens to the dinosaur genus Coelophysis . [21] In the case of the braincase later assigned to Postosuchus, in 2002 paleontologist David J. Gower argued that the specimen is not complete and may belong to an ornithodire. [22] Between 1932 and 1934, Case discovered other fossils of caudal vertebrae (UMMP 13670) in Rotten Hill, Texas, and a complete pelvis (UCMP V72183/113314) near Kalgary, Texas. [18] Within the same period, paleontologist Charles Lewis Camp collected over a hundred "rauisuchian" bones, from what is now the Petrified Forest National Park of Arizona, which belong to at least seven individuals (UCMP A296, MNA 207C). [18] Later, more remains came to light. In 1943, Case again described a pelvis along with a pubis (UM 23127) from the Dockum Group of Texas, which dates from the Carnian through the early Norian stages of Late Triassic period. [23] These early findings, from 1932 to 1943, were initially referred to as a new phytosaur reptile, but assigned forty years later to Postosuchus. [4]

The first articulated skeleton referred to P. kirkpatricki (CM 73372) was recovered by David S. Berman of the Carnegie Museum of Natural History, in Coelophysis Quarry at Ghost Ranch, New Mexico, between 1988 and 1989. [18] This specimen was composed of a well-preserved skeleton without skull and was described by Long and Murry in 1995, Weinbaum in 2002 and Novak in 2004. [24] [25] [26] The specimen represents a skeletally immature individual because none of the neural sutures are closed. It was referred to P. kirkpatricki by Long and Murry (1995) without specific justification, and more recent studies accepted this referral. [25] [26] [16] Nevertheless, Nesbitt (2011) noted that these studies failed to note any synapomorphies unique to P. kirkpatricki and CM 73372. Weinbaum (2002) and Novak (2004) even noted that the preacetabular process of the ilium in CM 73372 was much longer than that of P. kirkpatricki. Nesbitt (2011) also noted that CM 73372 differs from P. kirkpatricki and Rauisuchus in possessing a concave ventral margin of the ilium, and from P. alisonae in processing an asymmetrical distal end of the fourth metatarsal. Nesbitt (2011) couldn't differentiate CM 73372 and Polonosuchus as they overlap only in the caudal vertebrae. A phylogenetic analysis conducted by Nesbitt (2011), one of the most extensive on archosaurs, found CM 73372 to be the most basal crocodylomorph, thus referable neither to P. kirkpatricki nor to Rauisuchidae. [27]

In their description of Vivaron , Lessner et al. (2016) questioned the random referral of all rauisuchid material from the southwestern US to Postosuchus, saying that the discovery of Vivaron stresses the need for a re-appraisal of all material from localities younger or older than unequivocal remains of Postosuchus and Vivaron. [28]

Paleoecology

Postosuchus and Desmatosuchus HMNS Postosuchus and Desmatosuchus.jpg
Postosuchus and Desmatosuchus

Postosuchus lived in a tropical environment. [29] [4] The moist and warm region consisted of ferns, such as Cynepteris , Phelopteris and Clathropteris , gymnosperms, represented by Pelourdea , Araucarioxylon , Woodworthia , Otozamites and Dinophyton , and cycads like Sanmiguelia . [4] [30] Plants of the Dockum Group are not well known since the oxidizing of the environment has destroyed most of the plant fossils. [4] Some of them may, however, provide information about the climate in Dockum Group during the late Triassic period. For example, the discovery of large specimens belonging to Araucarioxylon determine that the region was well watered. [4] [31]

Postosuchus was one of the largest animals in that ecosystem and preyed on herbivores in the uplands like the dicynodont Placerias . The fauna found in Dockum Group confirm that there were lakes and/or rivers containing fish such as the cartilaginous Xenacanthus , the lobe-finned Chinlea and the dipnoan Ceratodus . On the margins of these rivers and in the uplands lived labyrinthodonts ( Latiscopus ) and reptiles such as Malerisaurus and Trilophosaurus , and even the archosaurs Coelophysis, Desmatosuchus , Typothorax , Leptosuchus , Nicrosaurus and Rutiodon . [4]

Notes

  1. ↑ Walking with Dinosaurs: The Evidence. DK publishing. 2001. ISBN   9780789471673.
  2. ↑ Gaines, Richard M. (2001). Coelophysis. ABDO Publishing Company. p. 20. ISBN   1-57765-488-9.
  3. 1 2 3 4 5 Weinbaum, J. C. (2013). "Postcranial skeleton of Postosuchus kirkpatricki (Archosauria: Paracrocodylomorpha), from the upper Triassic of the United States". Geological Society, London, Special Publications. 379 (1): 525–553. Bibcode:2013GSLSP.379..525W. doi:10.1144/SP379.7. S2CID   129092753.
  4. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Chatterjee, S. (1985). "Postosuchus, a new Thecodontian reptile from the Triassic of Texas and the origin of Tyrannosaurs". Philosophical Transactions of the Royal Society of London. B, Biological Sciences. 309 (1139). The Royal Society: 395–460. Bibcode:1985RSPTB.309..395C. doi:10.1098/rstb.1985.0092. ISSN   0080-4622.
  5. ↑ Julia Brenda Desojo, Randall B. Irmis, Sterling J. Nesbitt (2013). Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and Their Kin. Geological Society. p. 527. ISBN   9781862393615 . Retrieved 14 September 2022.{{cite book}}: CS1 maint: multiple names: authors list (link)
  6. ↑ Peyer et al. (2008), p. 370.
  7. ↑ Peyer et al. (2008), p. 368.
  8. 1 2 3 Peyer et al. (2008), p. 380.
  9. ↑ Long and Murry (1995), p. 139.
  10. ↑ Hutson, Joel D.; Hutson, K.N (March 2015). "Inferring the prevalence and function of finger hyperextension in Archosauria from finger-joint range of motion in the American alligator". Journal of Zoology. 296 (3): 189–199. doi:10.1111/jzo.12232 . Retrieved March 30, 2023.
  11. ↑ Hartman, Scott A.; Lovelace, David M.; Linzmeier, Benjamin J.; Mathewson, Paul D.; Porter, Warren P. (November 2022). "Mechanistic Thermal Modeling of Late Triassic Terrestrial Amniotes Predicts Biogeographic Distribution". Diversity. 14 (11): 973. doi: 10.3390/d14110973 . ISSN   1424-2818.
  12. ↑ Chatterjee (1985), p. 398–399.
  13. 1 2 Long and Murry (1995), pp. 148–162.
  14. ↑ Long and Murry (1995), pp. 154–162.
  15. ↑ Nesbitt and Norrell (2006), pp. 1045–1048.
  16. 1 2 3 Peyer et al. (2008), p. 365.
  17. 1 2 3 4 Peyer et al. (2008), p. 363.
  18. 1 2 3 4 5 Peyer et al. (2008), pp. 363–364.
  19. ↑ Case (1922), pp. 78–80.
  20. ↑ Case (1922), pp. 70–74.
  21. ↑ Case (1932), pp. 81–82.
  22. ↑ Gower (2002), p. 66.
  23. ↑ Case (1943), pp. 201–203.
  24. ↑ Long and Murry (1995), pp. 120–141.
  25. 1 2 Weinbaum (2002), 78 pp.
  26. 1 2 Novak (2004), 78 pp.
  27. ↑ Nesbitt, S. J. (2011). "The Early Evolution of Archosaurs: Relationships and the Origin of Major Clades". Bulletin of the American Museum of Natural History. 352: 1–292. doi: 10.1206/352.1 . hdl: 2246/6112 . S2CID   83493714.
  28. ↑ Lessner, EJ; Stocker, MR; Smith, ND; Turner, AH; Irmis, RB; Nesbitt, SJ (2016). "A new rauisuchid (Archosauria, Pseudosuchia) from the Upper Triassic (Norian) of New Mexico increases the diversity and temporal range of the clade". PeerJ. 4: e2336. doi: 10.7717/peerj.2336 . PMC   5018681 . PMID   27651983.
  29. ↑ Dunay (1972), 370 pp.
  30. ↑ Ash (1976), pp. 799–804.
  31. ↑ Ash (1972), pp. 124–128.

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References

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