The name Ctenochasma was coined by the German paleontologist Christian Erich Hermann von Meyer in 1852, based on a single lower jaw full of closely packed teeth which he gave the species name Ctenochasma roemeri.[1] A second species, C. gracile, was named by Oppel in 1862 based on a fragmentary skull.[2] However, a year earlier, another, more complete specimen probably belonging to the same species was described and named Pterodactylus elegans by Wagner. Because the species name elegans was named before gracile, the species is now known as Ctenochasma elegans. Another specimen originally attributed to a small or juvenile Pterodactylus, P. brevirostris (Wellnhofer's "example 29", which was later placed in its own genus Ptenodracon), probably represents a young juvenile Ctenochasma based on similar wing bone proportions that differ from the similar Aurorazhdarcho.[3] An additional species, C. porocristata, was named by Paul de Buisonjé in 1981. However, it was differentiated mainly by the presence of a crest along the snout, which has since been shown to be a feature related to growth or sex, rather than species.[4]
A fourth species of Ctenochasma was first described (but not named) by Philippe Taquet in 1972.[5] A single specimen, consisting of a partial skull with complete brain case, was found in France and housed in the collections of the Saint-Dizier Museum. Detailed comparison to other Ctenochasma specimens in 2004 confirmed that it was a new species.[6] In honor of Taquet's work on the specimen, Christopher Bennett named the species C. taqueti in 2007.[7]
Although researchers in the late 1990s and early 2000s, including Bennett and Jouve, suggested that all these species probably represented growth stages on just one kind of Ctenochasma, in a more comprehensive 2007 study, Bennett demonstrated that three distinct species could be recognized based on the number and slenderness of the teeth, which varied across all growth stages. C. roemeri, the earliest species, is characterized by its relatively low number of only moderately slender teeth. The later C. taqueti had a moderate number of slender teeth, and the last species, C. elegans, had a high number of very slender teeth. These three species, arranged chronologically, probably represent a single evolutionary lineage in which the filter-feeding apparatus was gradually refined.[7]
Description
Fossil skull of a subadult C. elegansFossil specimen of a young juvenile C. elegans
Ctenochasma is distinguished mainly by its numerous (over 400 in adults) long, thin, curved and closely packed teeth, which lined its elongated and narrow snout. The teeth were so closely packed that they formed a comb, and in adults they projected outward away from the jaws, forming a basket; traditionally, these are thought to indicate a filter feeding lifestyle, straining water through the teeth in order to capture and eat small invertebrates, but unlike the related Pterodaustro it lacks adaptations that would form a pumping mechanism. Instead, the spatulate profile formed by the teeth probably indicate a spoonbill-like lifestyle, increasing the surface area of the jaws in order to catch small prey.[8] The snout curved slightly upward and was rounded at the tip, and the teeth were restricted to the front half of the jaws.[6]
The smallest species, Ctenochasma elegans, had a maximum wingspan of 1.9 metres (6.2 ft) as an adult.[9]Ctenochasma is distinguished by its mouth which contained as many as 260 long, thin comb-like teeth. Adult Ctenochasma had a bony crest along the skull, though this is not found in juveniles.[4]
Comparisons between the scleral rings of both Ctenochasma elegans and Ctenochasma taqueti and modern birds and reptiles suggest that these taxa may have been nocturnal, and may have had activity patterns similar to modern nocturnal seabirds. This may also indicate niche partitioning with contemporary pterosaurs inferred to be diurnal, such as Pterodactylus and Scaphognathus.[10]
Compared to other ctenochasmatoids, it had larger wings, and may have displayed a flying style comparable to that of modern skuas.[8]
Classification
Skeletal reconstruction
Below is cladogram following a topology by Andres, Clark and Xu (2014). In the analysis, they recovered Ctenochasma within the family Ctenochasmatidae, more precisely within the subfamily Ctenochasmatinae, sister taxon to the tribe Pterodaustrini.[11]
^Oppel A. (1862). "Über Fährten im lithographischen Schiefer. Paläontologische Mitteilungen aus dem Museum des Koenigl." Bayrischen Staates, ed. A. Oppel, vol. 1, pp. 121–125 & pl. 39. Stuttgart: Ebner & Sembek.
^Bennett, S. Christopher (2013). "New information on body size and cranial display structures of Pterodactylus antiquus, with a revision of the genus". Paläontologische Zeitschrift. 87 (2): 269–289. doi:10.1007/s12542-012-0159-8. S2CID83722829.
^ abBennett, S.C. (1996). "Year-classes of pterosaurs from the Solnhofen Limestone of Germany: Taxonomic and Systematic Implications". Journal of Vertebrate Paleontology. 16 (3): 432–444. doi:10.1080/02724634.1996.10011332.
^Taquet, P. (1972). "Un crane de Ctenochasma (Pterodactyloidea) du Portlandien infe rieur de la Haute-Marne, dans les collections du Musee de St-Dizier". Comptes Rendus de l'Académie des Sciences. 174: 362–364.
^ abJouve, S. (2004). "Description of the skull of a Ctenochasma (Pterosauria) from the latest Jurassic of eastern France, with a taxonomic revision of European Tithonian Pterodactyloidea". Journal of Vertebrate Paleontology. 24 (3): 542–554. doi:10.1671/0272-4634(2004)024[0542:dotsoa]2.0.co;2. S2CID86019483.
^ abBennett, S.C. (2007). "A review of the pterosaur Ctenochasma: taxonomy and ontogeny". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 245 (1): 23–31. doi:10.1127/0077-7749/2007/0245-0023.
^ abWilton, Mark P. (2013). Pterosaurs: Natural History, Evolution, Anatomy. Princeton University Press. ISBN978-0691150611.
^Bennett, S.C. (2018). "New smallest specimen of the pterosaur Pteranodon and ontogenetic niches in pterosaurs". Journal of Paleontology. 92 (2): 254–271. doi:10.1017/jpa.2017.84. S2CID90893067.
