Ctenochasma Temporal range: Late Jurassic | |
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Fossil specimen of a juvenile C. elegans | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Order: | † Pterosauria |
Suborder: | † Pterodactyloidea |
Family: | † Ctenochasmatidae |
Subfamily: | † Ctenochasmatinae |
Genus: | † Ctenochasma Meyer, 1852 |
Type species | |
†Ctenochasma roemeri Meyer, 1852 | |
Other species | |
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Synonyms | |
Genus synonymy
Synonyms of C. elegans
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Ctenochasma (meaning "comb jaw") is a genus of Late Jurassic ctenochasmatid pterosaur belonging to the suborder Pterodactyloidea. Three species are currently recognized: C. roemeri (named after Friedrich Adolph Roemer), C. taqueti, and C. elegans. Their fossilized remains have been found in the Solnhofen Limestone of Bavaria, Germany, the "Purbeck Group" of northeastern Germany, and the Calcaires tâchetés of eastern France.
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]
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]
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]
Pterodactylus is a genus of extinct pterosaurs. It is thought to contain only a single species, Pterodactylus antiquus, which was the first pterosaur to be named and identified as a flying reptile and one of the first prehistoric reptiles to ever be discovered.
Pterosaurs are an extinct clade of flying reptiles in the order Pterosauria. They existed during most of the Mesozoic: from the Late Triassic to the end of the Cretaceous. Pterosaurs are the earliest vertebrates known to have evolved powered flight. Their wings were formed by a membrane of skin, muscle, and other tissues stretching from the ankles to a dramatically lengthened fourth finger.
Rhamphorhynchus is a genus of long-tailed pterosaurs in the Jurassic period. Less specialized than contemporary, short-tailed pterodactyloid pterosaurs such as Pterodactylus, it had a long tail, stiffened with ligaments, which ended in a characteristic soft-tissue tail vane. The mouth of Rhamphorhynchus housed needle-like teeth, which were angled forward, with a curved, sharp, beak-like tip lacking teeth, indicating a diet mainly of fish; indeed, fish and cephalopod remains are frequently found in Rhamphorhynchus abdominal contents, as well as in their coprolites.
Scaphognathus was a pterosaur that lived around Germany during the Late Jurassic. It had a wingspan of 0.9 m (3 ft).
Dorygnathus was a genus of rhamphorhynchid pterosaur that lived in Europe during the Early Jurassic period, when shallow seas flooded much of the continent. It had a short wingspan, and a relatively small triangular sternum, which is where its flight muscles attached. Its skull was long and its eye sockets were the largest opening therein. Large curved fangs that "intermeshed" when the jaws closed featured prominently at the front of the snout while smaller, straighter teeth lined the back. Having two or more morphs of teeth, a condition called heterodonty, is rare in modern reptiles but more common in basal ("primitive") pterosaurs. The heterodont dentition in Dorygnathus is consistent with a piscivorous (fish-eating) diet. The fifth digit on the hindlimbs of Dorygnathus was unusually long and oriented to the side. Its function is not certain, but the toe may have supported a membrane like those supported by its wing-fingers and pteroids. Dorygnathus was according to David Unwin related to the Late Jurassic pterosaur Rhamphorhynchus and was a contemporary of Campylognathoides in Holzmaden and Ohmden.
Germanodactylus is a genus of germanodactylid pterodactyloid pterosaur from Upper Jurassic-age rocks of Germany, including the Solnhofen Limestone. Its specimens were long thought to pertain to Pterodactylus. The head crest of Germanodactylus is a distinctive feature.
Anhanguera is a genus of pterodactyloid pterosaur known from the Early Cretaceous Romualdo Formation of Brazil and the Late Cretaceous Kem Kem Group of Morocco. This pterosaur is closely related to Ornithocheirus, but belongs in the family Anhangueridae. The generic name comes from the Tupi words añanga, meaning "spirit protector of the animals" + wera "bygone".
Gnathosaurus is a genus of ctenochasmatid pterosaur containing two species: G. subulatus, named in 1833 from the Solnhofen Limestone of Germany, and G. macrurus, known from the Purbeck Limestone of the UK. Its fossil remains dated back to the Late Jurassic period.
Gallodactylidae is a group of pterosaurs within the suborder Pterodactyloidea. Gallodactylids differed from other related pterosaurs in several distinct features, including fewer than 50 teeth present only in the jaw tips, and rounded crests present on the rear portion of the skull and jaws but not near the ends of their snouts. At least some species possessed jaw flanges, possibly used to bissect hard-shelled prey.
Cycnorhamphus is a genus of gallodactylid ctenochasmatoid pterosaur from the Late Jurassic period of France and Germany, about 152 million years ago. It is synonymous with the genus Gallodactylus.
Diopecephalus is a genus of pterodactyloid pterosaur from the Lower Tithonian of the Lithographic Limestone, Bavaria, Germany. The type and only species is D. kochi, although the name has been applied to Pterodactylus longicollum, with longicollum erroneously listed as the type species.
Prejanopterus is an extinct genus of pterodactyloid pterosaur from the Lower Cretaceous layers of the Leza Formation of La Rioja, Spain.
Euctenochasmatia is an extinct group of pterodactyloid pterosaurs. It was named by David Unwin in 2003 as the group that contains the most recent common ancestor of Pterodactylus and Ctenochasma, and all their descendants.
Aurorazhdarcho is an extinct genus of ctenochasmatoid pterosaur known from the Late Jurassic period of what is now Bavaria, southern Germany.
Ardeadactylus is an extinct genus of ctenochasmatoid pterosaur known from the Late Jurassic Solnhofen limestone of Bavaria, southern Germany. It contains a single species, Ardeadactylus longicollum, which was originally thought to be a species of Pterodactylus, as P. longicollum.
Cimoliopterus is a genus of pterosaur that lived during the Late Cretaceous in what is now England and the United States. The first known specimen, consisting of the front part of a snout including part of a crest, was discovered in the Grey Chalk Subgroup of Kent, England, and described as the new species Pterodactylus cuvieri in 1851. The specific name cuvieri honours the palaeontologist George Cuvier, whereas the genus Pterodactylus was then used for many pterosaur species that are not thought to be closely related today. It was among the first pterosaurs to be depicted as sculptures, in Crystal Palace Park in the 1850s. The species was subsequently assigned to various other genera, including Ornithocheirus and Anhanguera. In 2013, the species was moved to a new genus, as Cimoliopterus cuvieri; the generic name Cimoliopterus is derived from the Greek words for "chalk" and "wing". Other specimens and species have also been assigned to or synonymised with the species with various levels of certainty. In 2015, a snout discovered in the Britton Formation of Texas, US, was named as a new species in the genus, C. dunni; the specific name honours its collector, Brent Dunn.
Ikrandraco is a genus of lonchodraconid pterodactyloid pterosaur known from the Lower Cretaceous Jiufotang Formation of northeastern China, and the Cambridge Greensand of England. It is notable for its unusual skull, which features a crest on the lower jaw.
Aerodactylus is a pterosaur genus containing a single species, Aerodactylus scolopaciceps, previously regarded as a species of Pterodactylus.
This timeline of pterosaur research is a chronologically ordered list of important fossil discoveries, controversies of interpretation, and taxonomic revisions of pterosaurs, the famed flying reptiles of the Mesozoic era. Although pterosaurs went extinct millions of years before humans evolved, humans have coexisted with pterosaur fossils for millennia. Before the development of paleontology as a formal science, these remains would have been interpreted through a mythological lens. Myths about thunderbirds told by the Native Americans of the modern Western United States may have been influenced by observations of Pteranodon fossils. These thunderbirds were said to have warred with water monsters, which agrees well with the co-occurrence of Pteranodon and the ancient marine reptiles of the seaway over which it flew.
Forfexopterus is a genus of ctenochasmatid pterosaur from the Early Cretaceous Jiufotang Formation in China. It contains a single species, F. jeholensis, named from a mostly complete skeleton by Shunxing Jiang and colleagues in 2016. A second specimen, consisting of a wing, was described in 2020. While the first specimen is larger, it shows signs of being less mature than the second specimen, indicating that the developmental trajectories of Forfexopterus were variable. Like other ctenochasmatids, Forfexopterus had a long, low skull filled with many slender teeth; unlike other members of the group, however, it did not have a spatula-shaped snout tip or crests, and its teeth were more curved. A single characteristic distinguishes Forfexopterus from all other members of the wider group Archaeopterodactyloidea: of the four phalanx bones in its wing finger, the first was shorter than the second but longer than the third.