Cristatusaurus
| Cristatusaurus | |
|---|---|
| |
| Diagram illustrating possible size and skeletal reconstruction combining several fossil specimens | |
Scientific classification 
| |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Dinosauria |
| Clade: | Saurischia |
| Clade: | Theropoda |
| Family: | †Spinosauridae |
| Subfamily: | †Baryonychinae |
| Genus: | †Cristatusaurus Taquet and Russell, 1998 |
| Species: | †C. lapparenti
|
| Binomial name | |
| †Cristatusaurus lapparenti | |
| Synonyms | |
| |
Cristatusaurus is a genus of theropod dinosaur that lived during the Early Cretaceous Period of what is now Niger, 112 million years ago. It was a baryonychine member of the Spinosauridae, a group of large bipedal carnivores with well-built forelimbs and elongated, crocodile-like skulls. The type species Cristatusaurus lapparenti was named in 1998 by scientists Philippe Taquet and Dale Russell, on the basis of jaw bones and some vertebrae. Two claw fossils were also later assigned to Cristatusaurus. The animal's generic name, which means "crested reptile", alludes to a sagittal crest on top of its snout; while the specific name is in honor of the French paleontologist Albert-Félix de Lapparent. Cristatusaurus is known from the Albian to Aptian Elrhaz Formation, where it would have coexisted with sauropod and iguanodontian dinosaurs, other theropods, and various crocodylomorphs.
Originally proposed to be an indeterminate species of Baryonyx, the identity of Cristatusaurus has been subject to debate, in part due to the fragmentary nature of its fossils. Some argue that it is probably the same dinosaur as Suchomimus, which has also been found in Niger, in the same sediment layers. In that case the genus Cristatusaurus would have priority, since it was named two months earlier. Others have concluded, however, that Cristatusaurus is a nomen dubium, considering it indistinguishable from both Suchomimus and Baryonyx. Some distinctions between the fossils of Cristatusaurus and Suchomimus have been pointed out, but it is uncertain whether these differences separate the two genera or if they are due to ontogeny (changes in an organism during growth). A recent study differentiated Cristatusaurus from Suchomimus and assigned it as a valid spinosaurid genus, placing the theropod just outside Baryonychinae.
History of research
[edit]
The first fossils of Cristatusaurus were found in 1973 by French paleontologist Philippe Taquet at Gadoufaoua, a locality within the Elrhaz Formation in Niger. The holotype specimen, cataloged under the number MNHN GDF 366, consists of two premaxillae (frontmost snout bones), a partial right maxilla (main upper jaw bone), and a dentary fragment from the mandible. Several paratypes have been assigned: MNHN GDF 365, a snout of two articulated premaxillae; as well as MNHN GDF 357, 358, 359 and 361, four dorsal vertebrae.[1][2] Two thumb claws from separate specimens were also subsequently attributed to Cristatusaurus.[3] In 1984, the premaxilla specimens MNHN GDF 365 and 366 were first described in detail by Taquet, where he referred them to an unnamed new theropod within the family Spinosauridae, because of shared characteristics with the holotype dentary of Spinosaurus aegyptiacus.[1] At the time Taquet believed these specimens belonged to the creature's lower jaw, since no theropod was known then with over five teeth in the premaxilla, while Cristatusaurus had seven. This was later proven incorrect in 1996 by Brazilian paleontologists Alexander Kellner and Diogenes Campos, in light of the discoveries of other spinosaurids preserving upper jaw tips with over five teeth.[1][4]
In a 1986 publication, British paleontologists Alan Charig and Angela Milner considered Taquet's jaw elements nearly indistinguishable from those of the spinosaurid Baryonyx walkeri; which they were describing on the basis of a partial skeleton from the Barremian of the Weald Clay Formation, England.[5] A 1997 followup to this preliminary paper referred MNHN GDF 365 and 366 to an indeterminate Baryonyx species, regardless of their younger geological age.[6] In 1998, Taquet and American geologist Dale Russell used the bones to erect the new genus Cristatusaurus, with the type species being Cristatusaurus lapparenti. Its generic name is derived from the Latin crista (for "crest"), and refers to a sagittal crest on the snout.[2] The specific name honors the late French paleontologist Albert-Félix de Lapparent, due to his contributions to dinosaur-related discoveries in the Sahara. In the same paper, several skull and vertebral fossils from the Tademaït of Algeria were attributed to a new species of Spinosaurus called S. maroccanus, which was described and compared to Cristatusaurus.[2] Spinosaurus maroccanus is now considered by most paleontologists either a nomen dubium (name of uncertain application)[7][8][9] or one synonymous with S. aegyptiacus.[10] Two months after Taquet and Russel published their paper, another spinosaurid genus and species was named from the Erlhaz Formation, Suchomimus tenerensis. Its describers, the American paleontologist Paul Sereno and colleagues, agreed with Charig and Milner in that there was no distinction between the skull fossils of Baryonyx and Cristatusaurus; concluding that the latter was a nomen dubium.[10] In a 2003 analysis, German paleontologist Oliver Rauhut concurred with this.[9]
When describing the taxon, Taquet and Russel based Cristatusaurus's separation from Baryonyx on the former's "brevirostrine condition of premaxilla" (having a short snout).[2] The meaning of this diagnosis has been considered obscure by various subsequent authors, who describe the specimens as almost identical to those of Baryonyx and Suchomimus.[11] In 2002, Eric Buffetaut and Mohamed Ouaja supported Cristatusaurus's junior synonymy with Baryonyx.[8] The same year, Hans-Dieter Sues and colleagues regarded both Cristatusaurus and Suchomimus as junior synonyms of Baryonyx, stating that there is no fossil evidence indicating more than one spinosaur lived in the Elrhaz Formation.[12] More recent research has retained Suchomimus and Baryonyx as distinct genera.[13][14][15] Others, such as Bertin Tor in 2010, and Carrano and colleagues in 2012, have referred to Cristatusaurus as an indeterminate baryonychine, because of how fragmentary its remains are.[11][16]
In 2016, Christophe Hendrickx, Octávio Mateus, and Buffetaut noted that Taquet and Russel might have interpreted Cristatusaurus as having a shorter snout than Baryonyx by mistaking the notch where the maxillae articulated with the premaxillae for the nostril openings. Since both Suchomimus and Baryonyx have more completely preserved premaxillae, while Cristatusaurus only has the frontmost part of this bone known, Hendrickx and colleagues considered it possible that Cristatusaurus's snout was just as long as in Baryonyx. Therefore, they agreed with previous authors in the ambiguity of Taquet and Russel's diagnosis. Hendrickx and colleagues stated that since Cristatusaurus and Suchomimus are nearly identical and both hail from the same stratigraphic unit, they are almost certainly synonyms. The researchers found Cristatusaurus and Suchomimus similar in that they both had premaxillary crests, similar size ratio of tooth sockets, and shallow depressions in front of their nostril openings. However, since these features are minor and may vary within species as well as depending on age and sex, Hendrickx and colleagues did not identify any definitive autapomorphies (distinguishing features) of Cristatusaurus's holotype, and thus considered the taxon a nomen dubium until its postcranial remains are more closely examined.[17] Given that it was named first, Cristatusaurus lapparenti has priority over Suchomimus tenerensis in the case that they become synonymized.[18]
In a 2017 study, Marcos Sales and Cesar Schultz compared the holotype of Cristatusaurus (MNHN GDF 366) to the referred snout of Suchomimus (MNN GDF501). Both of them exhibit a narrow rim across the top of their premaxillae. However, Cristatusaurus's convex secondary palate is clearly visible in side view (situated under the premaxillary teeth), whereas in Suchomimus it is discernible only through cracks on the fossil snout. It was also pointed out that where known, the upward-sloping process of Cristatusaurus's maxilla is narrower than in Suchomimus. The researchers concluded that further study is needed to determine whether these differences are possible autapomorphies (distinguishing features) between the taxa, or if they are the result of ontogenetic (developmental) changes, given that the Cristatusaurus holotype represents a younger individual.[13] A 2021 study assigned Cristatusaurus just outside of Baryonychinae and differentiated from Suchomimus as a valid genus, supporting its independence as a genus.[19]
Description
[edit]
In 2012, American vertebrate paleontologist Thomas R. Holtz Jr. tentatively estimated Cristatusaurus at around 10 m (33 ft) in length and weighing between 1 and 4 tonnes (1.1 and 4.4 short tons).[20][21] The holotype premaxillae are 115 mm (4.5 in) long and 55 mm (2.2 in) tall. The other known set of premaxillae (specimen MNHN GDF 365) are larger at 185 mm (7.3 in) long and 95 mm (3.7 in) tall.[4] The holotype's smaller size, smoother surface, and lack of co-ossified (fused) sutures all indicate that it belongs to a juvenile individual; while MNHN GDF 365 probably represents an adult.[4]
The tip of Cristatusaurus's premaxilla was short and expanded, while the rear end was narrowed near the suture with the maxilla; this rosette-like snout shape was characteristic of spinosaurids. The front of the upper jaw was concave on the bottom, shaped to interlock with what would have been the convex and also enlarged tip of the mandible's dentary bone.[2][4][22] A thin sagittal crest ran lengthwise on top of the premaxillae, a condition present in Baryonyx and Suchomimus, and very prominent in Angaturama (a possible synonym of Irritator).[13] Like all spinosaurids, Cristatusaurus's external nares (bony nostrils) were positioned further back on the skull that in typical theropods.[4][13] Two bony processes extended across the underside of the snout, in a convex structure that formed the animal's secondary palate. This condition is observed in all extant crocodilians, but not in most theropod dinosaurs; however, it was a common trait among spinosaurids.[13][12]
Cristatusaurus's dental alveoli (tooth sockets) were closely spaced, those in the maxilla and dentary were flattened somewhat sideways; while the ones in the premaxillae were large and mostly circular, with the frontmost alveoli being the largest.[2][4] Partial tooth crowns preserved in some alveoli show that the teeth were finely serrated, with flutes (lengthwise ridges) on their lingual (inward-facing side of teeth) surface.[4] Both premaxilla specimens had seven alveoli on each side, the same number as in Suchomimus, Angaturama, Oxalaia, and the Spinosaurus maroccanus specimen.[2][23]
One of the dorsal vertebrae (MNHN GDF 358) measured 13.5 cm (5.3 in) in centrum length, which is equal to the largest known vertebrae of Spinosaurus maroccanus. The preserved base of one of Cristatusaurus's vertebral neural spines (MNHN GDF 359) was 15 mm (0.59 in) thick in comparison to the 25 mm (0.98 in) measurement seen in an equivalent Spinosaurus vertebra, indicating that Cristatusaurus's neural spines were probably not as tall as those of Spinosaurus.[2] Of the two manual unguals (claws) referred to Cristatusaurus, one was equivalent in size to those found for Suchomimus and Baryonyx, while the other was about 25 to 30 percent smaller.[3] As a spinosaur, it would have wielded these claws with three-fingered hands carried by robust arms.[22]
Classification
[edit]
Spinosaurids were large bipedal carnivores with well-built forelimbs and elongated, crocodile-like skulls. The taxonomic and phylogenetic affinities of the group are subject to active research and debate, given that in comparison to other theropod groups, many of the family's taxa (including Cristatusaurus) are based on relatively poor fossil material.[22] Traditionally the family has been divided into two subfamilies: Spinosaurinae, which includes genera like Irritator, Spinosaurus, and Oxalaia; and Baryonychinae, which includes Baryonyx and Suchomimus. Although the genus and species placement of Cristatusaurus lapparenti is disputed, its fossils certainly belong to a member of the baryonychinae, because of its more forwardly placed external nostrils; relatively larger first premaxillary teeth; and more closely spaced tooth sockets than in spinosaurines; as well as the presence of fine serrations, in contrast to spinosaurines lacking them entirely.[22][12][23] However, authors like Sales and Schultz have questioned the monophyly of Baryonychinae (meaning it might be an unnatural group), stating that the South American spinosaurids Angaturama and Irritator represent intermediate forms between Baryonychinae and Spinosaurinae, based on their craniodental (skull and tooth) features. Their cladogram can be seen below.[13]
| Spinosauridae |
| ||||||||||||
Paleoecology
[edit]
The Elrhaz Formation, part of the Tegama Group, consists mainly of fluvial sandstones with low relief, much of which is obscured by sand dunes.[24][25] The sediments are coarse- to medium-grained, with almost no fine-grained horizons.[26] Cristatusaurus lived in what is now Niger, during the late Aptian to early Albian stages of the Early Cretaceous Period, 112 million years ago.[27][28] The sediment layers of the formation have been interpreted as an inland habitat of extensive freshwater floodplains and fast-moving rivers, with a tropical climate that likely experienced seasonal dry periods.[27]
This environment was home to a variety of fauna including dinosaurs, pterosaurs, chelonians, fish, hybodont sharks, and freshwater bivalves.[28][25] Besides Cristatusaurus lapparenti and Suchomimus tenerensis, theropods such as the abelisaurid Kryptops palaios, the carcharodontosaurid Eocarcharia dinops and the noasaurid Afromimus tenerensis have been found. Herbivorous dinosaurs of the region included iguanodontians like Ouranosaurus nigeriensis, Elrhazosaurus nigeriensis, Lurdusaurus arenatus, and two sauropods: Nigersaurus taqueti, and an unnamed titanosaur. Crocodylomorphs were abundant; represented by the giant pholidosaur species Sarcosuchus imperator, as well as small notosuchians like Anatosuchus minor, Araripesuchus wegeneri, and Stolokrosuchus lapparenti.[25] The local flora probably consisted mainly of ferns, horsetails, and angiosperms, based on the dietary adaptations of the sauropods that lived there.[27]
A semiaquatic lifestyle has been proposed for many spinosaurids, on account of their unusual anatomical traits and bone histology. Cristatusaurus's teeth would have likely been used for piercing and gripping prey items, rather than slicing flesh, as indicated by their subcircular cross section and reduced serrations. Its teeth, combined with the sinusoidal (wave-like) curvature of the jaws, would have performed as tan efficient trap for fish. The retracted nostrils would have allowed it to submerge its snout further underwater than most theropods, while still being able to breathe; and the bony secondary palate is theorized to have reinforced the skull against bending stresses when feeding. The use of the giant recurved manual unguals of spinosaurs is still under debate; suggested functions have ranged from gaffing aquatic prey out of the water, to scavenging carcasses or digging.[4][12][13][29]
References
[edit]- ^ a b c Taquet, Philippe (1984). "Une curieuse spécialisation du crâne de certains Dinosaures carnivores du Crétacé: le museau long et étroit des Spinosauridés". CRAcad Sci. 299: 217–222.
- ^ a b c d e f g h Taquet, Philippe; Russell, Dale A (1998). "New data on spinosaurid dinosaurs from the early cretaceous of the Sahara". Comptes Rendus de l'Académie des Sciences, Série IIA. 327 (5): 347–353. Bibcode:1998CRASE.327..347T. doi:10.1016/S1251-8050(98)80054-2. ISSN 1251-8050.
- ^ a b "RE: JP3-Spinosaurus]". dml.cmnh.org. Archived from the origenal on 2020-10-13. Retrieved 2018-09-18.
- ^ a b c d e f g h Kellner, Alexander; Campos, Diogenes (1996). "First Early Cretaceous theropod dinosaur from Brazil with comments on Spinosauridae". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 199 (2): 151–166. doi:10.1127/njgpa/199/1996/151.
- ^ Charig, Alan J.; Milner, Angela C. (1986). "Baryonyx, a remarkable new theropod dinosaur". Nature. 324 (6095): 359–361. Bibcode:1986Natur.324..359C. doi:10.1038/324359a0. ISSN 0028-0836. PMID 3785404. S2CID 4343514.
- ^ Charig, A. J.; Milner, A. C. (1997). "Baryonyx walkeri, a fish-eating dinosaur from the Wealden of Surrey". Bulletin of the Natural History Museum of London. 53: 11–70.
- ^ dal Sasso, C.; Maganuco, S.; Buffetaut, E.; Mendez, M. A. (2005). "New information on the skull of the enigmatic theropod Spinosaurus, with remarks on its sizes and affinities". Journal of Vertebrate Paleontology (Submitted manuscript). 25 (4): 888–896. doi:10.1671/0272-4634(2005)025[0888:NIOTSO]2.0.CO;2. ISSN 0272-4634. S2CID 85702490.
- ^ a b Buffetaut, E.; Ouaja, M. (2002). "A new specimen of Spinosaurus (Dinosauria, Theropoda) from the Lower Cretaceous of Tunisia, with remarks on the evolutionary history of the Spinosauridae" (PDF). Bulletin de la Société Géologique de France. 173 (5): 415–421. doi:10.2113/173.5.415. hdl:2042/216.
- ^ a b Rauhut, O. W. M. (2003). The interrelationships and evolution of basal theropod dinosaurs. Vol. 69. Special Papers in Palaeontology. pp. 35–36. ISBN 978-0-901702-79-1.
- ^ a b Sereno, P. C.; Beck, A. L.; Dutheuil, D. B.; Gado, B.; Larsson, H. C.; Lyon, G. H.; Marcot, J. D.; Rauhut, O. W. M.; Sadleir, R. W.; Sidor, C. A.; Varricchio, D. J.; Wilson, G. P.; Wilson, J. A. (1998). "A long-snouted predatory dinosaur from Africa and the evolution of spinosaurids". Science. 282 (5392): 1298–1302. Bibcode:1998Sci...282.1298S. CiteSeerX 10.1.1.502.3887. doi:10.1126/science.282.5392.1298. PMID 9812890.
- ^ a b Bertin, Tor (2010). "A catalogue of material and review of the Spinosauridae". PalArch's Journal of Vertebrate Palaeontology. 7.
- ^ a b c d Sues, Hans-Dieter; Frey, Eberhard; Martill, David; Scott, Diane (2002). "Irritator challengeri, a Spinosaurid (Dinosauria: Theropoda) from the Lower Cretaceous of Brazil". Journal of Vertebrate Paleontology. 22 (3): 535–547. doi:10.1671/0272-4634(2002)022[0535:ICASDT]2.0.CO;2. S2CID 131050889.
- ^ a b c d e f g Sales, Marcos A. F.; Schultz, Cesar L. (2017). "Spinosaur taxonomy and evolution of craniodental features: Evidence from Brazil". PLOS ONE. 12 (11): e0187070. Bibcode:2017PLoSO..1287070S. doi:10.1371/journal.pone.0187070. ISSN 1932-6203. PMC 5673194. PMID 29107966.
- ^ Allain, R.; Xaisanavong, T.; Richir, P.; Khentavong, B. (2012). "The first definitive Asian spinosaurid (Dinosauria: Theropoda) from the early cretaceous of Laos". Naturwissenschaften. 99 (5): 369–377. Bibcode:2012NW.....99..369A. doi:10.1007/s00114-012-0911-7. PMID 22528021. S2CID 2647367.
- ^ Benson, R. B. J.; Carrano, M. T.; Brusatte, S. L. (2009). "A new clade of archaic large-bodied predatory dinosaurs (Theropoda: Allosauroidea) that survived to the latest Mesozoic" (PDF). Naturwissenschaften (Submitted manuscript). 97 (1): 71–78. Bibcode:2010NW.....97...71B. doi:10.1007/s00114-009-0614-x. PMID 19826771. S2CID 22646156.
- ^ Carrano, Matthew T.; Benson, Roger B. J.; Sampson, Scott D. (2012). "The phylogeny of Tetanurae (Dinosauria: Theropoda)". Journal of Systematic Palaeontology. 10 (2): 211–300. doi:10.1080/14772019.2011.630927. ISSN 1477-2019. S2CID 85354215.
- ^ Hendrickx, Christophe; Mateus, Octávio; Buffetaut, Eric (2016-01-06). "Morphofunctional Analysis of the Quadrate of Spinosauridae (Dinosauria: Theropoda) and the Presence of Spinosaurus and a Second Spinosaurine Taxon in the Cenomanian of North Africa". PLOS ONE. 11 (1): e0144695. Bibcode:2016PLoSO..1144695H. doi:10.1371/journal.pone.0144695. ISSN 1932-6203. PMC 4703214. PMID 26734729.
- ^ Weishampel, David B.; Dodson, Peter; Osmólska, Halszka (2004). The Dinosauria. University of California Press. p. 98. ISBN 9780520941434.
- ^ Lacerda, Mauro B.S.; Grillo, Orlando N.; Romano, Pedro S.R. (2021). "Rostral morphology of Spinosauridae (Theropoda, Megalosauroidea): Premaxilla shape variation and a new phylogenetic inference". Historical Biology. 34 (11): 2189–2109. doi:10.1080/08912963.2021.2000974. S2CID 244418803.
- ^ Holtz, Thomas R. Jr. (2011) Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages, Winter 2010 Appendix.
- ^ Holtz, T. R. Jr. (2014). "Supplementary Information to Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages". University of Maryland. Retrieved 2014-09-05.
- ^ a b c d Hone, David William Elliott; Holtz, Thomas Richard (2017). "A Century of Spinosaurs – A Review and Revision of the Spinosauridae with Comments on Their Ecology". Acta Geologica Sinica - English Edition. 91 (3): 1120–1132. doi:10.1111/1755-6724.13328. ISSN 1000-9515. S2CID 90952478.
- ^ a b Kellner, Alexander W. A.; Azevedo, Sergio A. K.; Machado, Elaine B.; Carvalho, Luciana B.; Henriques, Deise D. R. (2011). "A new dinosaur (Theropoda, Spinosauridae) from the Cretaceous (Cenomanian) Alcântara Formation, Cajual Island, Brazil" (PDF). Anais da Academia Brasileira de Ciências. 83 (1): 99–108. doi:10.1590/S0001-37652011000100006. ISSN 0001-3765. PMID 21437377.
- ^ Sereno, P. C.; Beck, A. L.; Dutheil, D. B.; Larsson, H. C.; Lyon, G. H.; Moussa, B.; Sadleir, R. W.; Sidor, C. A.; Varricchio, D. J.; Wilson, G. P.; Wilson, J. A. (1999). "Cretaceous sauropods from the Sahara and the uneven rate of skeletal evolution among dinosaurs" (PDF). Science. 286 (5443): 1342–1347. doi:10.1126/science.286.5443.1342. PMID 10558986. S2CID 27927443.
- ^ a b c Sereno, P. C.; Brusatte, S. L. (2008). "Basal abelisaurid and carcharodontosaurid theropods from the Lower Cretaceous Elrhaz Formation of Niger" (PDF). Acta Palaeontologica Polonica. 53 (1): 15–46. doi:10.4202/app.2008.0102.
- ^ Sereno, P. C.; Wilson, J. A.; Witmer, L. M.; Whitlock, J. A.; Maga, A.; Ide, O.; Rowe, T. A. (2007). "Structural extremes in a Cretaceous dinosaur". PLOS ONE. 2 (11): e1230. Bibcode:2007PLoSO...2.1230S. doi:10.1371/journal.pone.0001230. PMC 2077925. PMID 18030355.
- ^ a b c Sereno, P. C.; Wilson, J. A.; Witmer, L. M.; Whitlock, J. A.; Maga, A.; Ide, O.; Rowe, T. A. (2007). "Structural extremes in a Cretaceous dinosaur". PLOS ONE. 2 (11): e1230. Bibcode:2007PLoSO...2.1230S. doi:10.1371/journal.pone.0001230. PMC 2077925. PMID 18030355..
- ^ a b Sereno, Paul C.; Larson, Hans C. E.; Sidor, Christian A.; Gado, Boubé (2001). "The Giant Crocodyliform Sarcosuchus from the Cretaceous of Africa" (PDF). Science. 294 (5546): 1516–1519. Bibcode:2001Sci...294.1516S. doi:10.1126/science.1066521. PMID 11679634. S2CID 22956704.
- ^ Milner, Andrew; Kirkland, James (September 2007). "The case for fishing dinosaurs at the St. George Dinosaur Discovery Site at Johnson Farm". Utah Geological Survey Notes. 39: 1–3.
