Biology:Redondasaurus

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Short description: Extinct genus of reptiles

Redondasaurus
Temporal range: Late Triassic (late Norian – Rhaetian)
Redondasaurus bermani at CMNH 04.jpg
Mounted skeleton of Redondasaurus bermani at the Carnegie Museum of Natural History
Scientific classification e
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Archosauromorpha
Clade: Archosauriformes
Order: †Phytosauria
Family: †Parasuchidae
Tribe: †Mystriosuchini
Genus: †Redondasaurus
Hunt & Lucas, 1993
Species
  • †R. gregorii
  • †R. bermani

Redondasaurus is an extinct genus or subgenus of phytosaur from the Late Triassic (late Norian or Rhaetian) of the southwestern United States. It was named by Hunt & Lucas in 1993, and contains two species, R. gregorii and R. bermani. It is the youngest and most evolutionarily-advanced of the phytosaurs.

Specimens

Original specimens (1939-1992)

OMNH 1250, the first Redondasaurus specimen to be discovered, was a slender skull found in 1939 by D.E. Savage. Savage discovered the skull in the Travesser Formation of New Mexico, and originally referred it to the genus Machaeroprosopus.[1] In 1947, another phytosaur skull (YPM 3294) was discovered by E.H. Colbert and J.T. Gregory in the Redonda Formation of New Mexico. Colbert & Gregory (1947) were the first to recognize that that both skulls may represent a new taxon. In addition, they proposed that the skulls represented the most derived phytosaur species in North America, due to their supratemporal fenestrae being hidden in dorsal view.[1]

CM 69727, the holotype skull of R. bermani

A third skull (CM 69727) was discovered by D.S. Berman in the 1980s. It was recovered from the Coelophysis Quarry of Ghost Ranch near Abiquiu, New Mexico.[1] The deposits of the Coelophysis Quarry have variably been referred to as the Rock Point Formation or the "siltstone member" of the Chinle Formation. Ballew (1989) referred the Ghost Ranch skull to Pseudopalatus (now Machaeroprosopus) buceros.[1]

Redondasaurus named (1993)

The genus Redondasaurus was named by A.P. Hunt and S.G. Lucas in 1993. The name Redondasaurus is derived from the Redonda Formation and the Greek word "saurus," meaning lizard. The Redonda Formation is named after Mesa Redonda near Tucumcari, New Mexico.[1][2] The authors had previously mentioned the unnamed phytosaur species in a 1992 paper on "Triassic Stratigraphy and Paleontology" in New Mexico.[3]

Hunt & Lucas (1993) named two new species for Redondasaurus. Redondasaurus gregorii consisted of Colbert & Gregory's Redonda Formation skull (which was termed the holotype) and Savage's Travesser Formation skull. Redondasaurus bermani was based on Berman's Ghost Ranch skull.[1]

Other specimens (1993–present)

Redondasaurus gregorii specimen NMMNH P-31094

Many additional specimens have been added to Redondasaurus apart from the three originally placed in the genus in 1993.[4] The first report from outside New Mexico, a skull impression (MNA V3498) from the Wingate Sandstone of Utah, was initially described by Morales & Ash (1993).[5][6] Several skulls from the Bull Canyon Formation of Texas were mentioned in a Master's thesis by Chavez (2010). A juvenile skull of R. gregorii (NMMNH P-44920) was first mentioned by Rinehart et al. (2009) and fully described by Lucas et al. (2013). It was collected from the Coelophysis Quarry, a site which had previously only produced the holotype of R. bermani.[7] Heckert et al. (2001) identified a massive flattened skull (NMMNH P-31094) from the Redonda Formation.

All specimens referred to Redondasaurus were discussed and redescribed by Spielmann & Lucas (2012). Several of the fossils were newly reported. The two most well-preserved skulls are from the Redonda Formation (an adult, NMMNH P-4983, and a juvenile, NMMNH P-31095). The oldest Redondasaurus specimen is an incomplete skull (UCMP V78034/119436) from the Petrified Forest Member (Chinle Formation) of Rio Arriba County, New Mexico. The authors also described a plethora of phytosaur postcranial bones from the Redonda Formation. The large sample of approximately 13 Redondasaurus gregorii skulls have helped to reconstruct growth series and sexual dimorphism trends in the species.[5]

Description

Redondasaurus, like other phytosaurs, had a very long snout. Known skull lengths range from 22 cm (0.72 ft) in juveniles to 120.5 cm (3.95 ft) in very large adults,[7] suggesting total lengths up to 6.4 m (21 ft).[2] The teeth of Redondasaurus have a columnar enamel microstructure while lines of arrested growth are rare. These characteristics are shared with other phytosaurs from Western North America, contrasting with those from Eastern North America ("Rutiodon").[8]

Differences between species

R. gregorii is distinguished by the lack of a rostral crest. Complete skulls of this species are uncommon, but some fragmentary narrow-snouted phytosaur specimens from the Redonda Formation may be part of the taxon.[1]:331

R. bermani is distinguished by the presence of a partial crest on the rostrum. Only one skull of this species has been found, but Hunt and Lucas postulate that "by analogy with other phytosaurs, it is likely that this crested species was sub-equal in abundance with [R. gregorii].".[1]:331

Diagnostic features

The diagnostic criteria given in 1993 for the new genus was as follows:

"Phytosaurid that differs from other genera in possessing supratemporal fenestrae that are essentially concealed in dorsal view and whose anterior margin only slightly emarginates the skull roof and has wide squamosal-postorbital bars.":331

Hunt and Lucas also extended Colbert and Gregory's analysis that Redondasaurus was the most derived North American phytosaurs, as:

"Phytosaurs show an evolutionary trend to displace ventrally the posterior portion of the midline of the skull roof. Redondasaurus represents the most advanced development of this character.":331

Additional diagnostic criteria were introduced in 2012 by J. Spielmann and S.G. Lucas.[9][10] These include:

  1. Reduced antorbital fenestra
  2. A prominent pre-infratemporal shelf
  3. A septomaxilla forming the anterolateral half of the external naris
  4. Thickened rim of the orbit
  5. Inflated posterior part of nasal
  6. Thickened dorsal osteoderms

Classification

Historically, studies of Redondasaurus have been hampered by small number of specimens available, of which only four skulls were recognized in literature. Recently, several Norian-Rhaetian phytosaur skulls have been referred to Redondasaurus, which has brought the number of recognized skulls to ten. These new specimens encompass a range of sizes from hatchlings to adults and possibly include the first evidence of sexual dimorphism in the taxon.[10]

Sexual dimorphism within Redondasaurus was also recognized by J. Spielman and S.G. Lucas on May 11, 2012, at the 64th Annual Meeting of the Geological Society of America.[4]

Validity

Disagreement on the validity of Redondasaurus emerged 1995, when Long and Murry did not accept it and referred to the specimen as Pseudopalatus pristinus instead. The reason for this may have been that the type specimen of Redondasaurus is missing the entire narial area, left side of its snout, the anterior two thirds of the right premaxilla, and most of its palate.[9] In addition to this, the term used by Savage to describe the first specimen found in 1939,[1] Machaeroprosopus, continues to be used by some scholars in place of Redondasaurus as the genus name.[9] Hungerbühler et al. argued in 2013 that Redondasaurus should be regarded as a junior synonym of Machaeroprosopus because:

  1. Upon a comparison of cranial characters, Machaeroprosopus lottorum is found to bridge the morphological gap between Redondasaurus and Machaeroprosopus in such a way that the distinction becomes arbitrary.
  2. According to cladistic analysis, it is unlikely that Redondasaurus is in a basal position compared to other North American pseudopalatine phytosaurs.
  3. For R. gregorii and R. bermani to be sister taxa, three additional steps would be necessary for forming a phylogenetic tree. This is the case even if the rostral crest, used by Lucas and Hunt to differentiate R. gregorii and R. bermani, is ignored in the analysis.[9]

Paleoecology

Placerias and Redondasaurus
Skeletal mount of Redondasaurus

The Chinle Group, where a large portion of Redondasaurus skulls have been found, is composed of fluvial and lacustrine sediments. Accumulations of fossils in the Chinle Formation can be found in floodplains, bogs, ponds, and fluvial channels. Additional paleontological and sedimentary evidence support the hypothesis that the climate of the Chinle was strongly influenced by high levels of precipitation.[11]

Most Redondasaurus fossils have been collected from north-central and eastern New Mexico, with a few other occurrences in Texas and Utah.[3][6] The Chinle Group is particularly important to paleontologists interested in aetosaurs, as it has been critical in establishing their biochronology in the Late Triassic.[12]

Redondasaurus is important because it serves as an index species for the Apachean Land Vertebrate Faunachron (LVF). Indeed, it is considered a true index fossil because Redondasaurus is temporally restricted and easily identified.[13] The biostratigraphic importance of the genus was reaffirmed when it was determined that the beginning of the Apachean was lower than previously concluded. Rather than at the base of the Redonda Formation, the Apachean appears high in the Bull Canyon Formation. Correlating the vertebrate stratigraphy of Redondasaurus has also allowed for the correlation of Redonda locally within the southwestern USA.[4] Given the recent acquisition of additional diagnostic characteristics, and the increase in number of Redondasaurus skulls recognized in literature, it is likely that the use of the genus as an index fossil will expand to other deposits and even globally.[10]

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 Hunt, Andrian P.; Lucas, Spencer G. (1993). "A new phytosaur (Reptilia: Archosauria) genus from the Uppermost Triassic of the Western United States and its biochronological significance". New Mexico Museum of Natural History & Science Bulletin 3: 193–196. https://www.researchgate.net/publication/283271847. 
  2. ↑ 2.0 2.1 "Redondasaurus". http://www.nmnaturalhistory.org/redondasaurus1.html. 
  3. ↑ 3.0 3.1 Lucas, SPENCER G., and ADRIAN P. Hunt. "Triassic stratigraphy and paleontology, Chama basin and adjacent areas, north-central New Mexico." New Mexico Geological Society Guidebook 43 (1992): 151-167.
  4. ↑ 4.0 4.1 4.2 "REVISION OF THE REDONDA FORMATION (UPPER TRIASSIC CHINLE GROUP) VERTEBRATE FAUNA AND ITS IMPACT ON THE APACHEAN LAND-VERTEBRATE FAUNACHRON". https://gsa.confex.com/gsa/2012RM/finalprogram/abstract_203297.htm. 
  5. ↑ 5.0 5.1 Spielmann, Justin A.; Lucas, Spencer G. (2012). "Tetrapod Fauna of the Upper Triassic Redona Formation East-central New Mexico: The Characteristic Assemblage of the Apachean Land-vertebrate Faunachron". New Mexico Museum of Natural History and Science Bulletin 55. https://books.google.com/books?id=r-woCgAAQBAJ. 
  6. ↑ 6.0 6.1 Martz, Jeffrey; Irmis, Randall; Milner, Andrew (2014-09-09). "Lithostratigraphy and biostratigraphy of the Chinle Formation (Upper Triassic) in southern Lisbon Valley, southeastern Utah". Utah Geological Association 43: 396–448. https://www.researchgate.net/publication/265550976. 
  7. ↑ 7.0 7.1 Lucas, Spencer G.; Spielmann, Justin A.; Rinehart, Larry F. (2013). "Juvenile skull of the phytosaur Redondasaurus from the Upper Triassic of New Mexico, and phytosaur ontogeny". New Mexico Museum of Natural History and Science, Bulletin 61: 389–399. https://www.researchgate.net/publication/280880541. 
  8. ↑ Miller-Cam, Jess A.; Heckert, Andrew B.; Hoffman, Devin (2021). "Tooth enamel microstructure in North American Phytosauria (Diapsida:Archosauriformes): Implications for biogeography and ecology of a Late Triassic clade of crocodylian-like predators" (in English). Palaeontologia Electronica 14 (3): 1–26. doi:10.26879/1162. ISSN 1094-8074. https://palaeo-electronica.org/content/2021/3440-phytosaur-tooth-enamel. 
  9. ↑ 9.0 9.1 9.2 9.3 Hungerbühler, Axel; Mueller, Bill; Chatterjee, Sankar; Cunningham, Douglas P. (September 2012). "Cranial anatomy of the Late Triassic phytosaur Machaeroprosopus, with the description of a new species from West Texas". Earth and Environmental Science Transactions of the Royal Society of Edinburgh 103 (3–4): 269–312. doi:10.1017/S1755691013000364. ISSN 1755-6929. 
  10. ↑ 10.0 10.1 10.2 "REVISION OF REDONDASAURUS GREGORII (ARCHOSAURIA: PARASUCHIDAE) FROM THE LATE TRIASSIC (NORIAN-RHAETIAN) OF NEW MEXICO". https://gsa.confex.com/gsa/2010AM/finalprogram/abstract_178169.htm. 
  11. ↑ Michael Parrish, J. (1989). "Vertebrate paleoecology of the Chinle formation (Late Triassic) of the Southwestern United States". Palaeogeography, Palaeoclimatology, Palaeoecology. XIIth INQUA Congress 72: 227–247. doi:10.1016/0031-0182(89)90144-2. ISSN 0031-0182. Bibcode: 1989PPP....72..227M. 
  12. ↑ Lucas, Spencer G.; Heckert, Andrew B. (1996). "Late Triassic aetosaur biochronology". Albertiana 17: 57–64. http://work.geobiology.cn/ebook/ALBERTIANA%20NO.17/12%20Late%20Triassic%20aetosaur%20biochronology.pdf. Retrieved 2015-03-06. 
  13. ↑ Lucas, Spencer G (November 1998). "Global Triassic tetrapod biostratigraphy and biochronology". Palaeogeography, Palaeoclimatology, Palaeoecology 143 (4): 347–384. doi:10.1016/S0031-0182(98)00117-5. ISSN 0031-0182. Bibcode: 1998PPP...143..347L. 

Further reading

  • The Great Rift Valleys of Pangea in Eastern North America By Peter M. LeTourneau, Paul Eric Olsen. Published 2003, Columbia University Press. ISBN:0-231-12676-X
  • Palaeogeography, Palaeoclimatology, Palaeoecology By Elsevier Science (Firm). Published 1998, Elsevier. v. 143. Original from the University of California.

External links

Wikidata ☰ Q596876 entry



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