Chuanqilong Temporal range: Early Cretaceous | |
---|---|
Holotype specimen | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Dinosauria |
Clade: | † Ornithischia |
Clade: | † Thyreophora |
Clade: | † Ankylosauria |
Family: | † Ankylosauridae |
Genus: | † Chuanqilong Han et al., 2014 |
Type species | |
†Chuanqilong chaoyangensis Han et al., 2014 |
Chuanqilong (meaning "legendary dragon") is a monospecific genus of basal ankylosaurid dinosaur from the Liaoning Province, China that lived during the Early Cretaceous (late Barremian to Aptian stage, 122.0 to 118.9 Ma) in what is now the Jiufotang Formation. The type and only species, Chuanqilong chaoyangensis, is known from a nearly complete skeleton with a skull of a juvenile individual. It was described in 2014 by Fenglu Han, Wenjie Zheng, Dongyu Hu, Xing Xu, and Paul M. Barrett. Chuanqilong shows many similarities with Liaoningosaurus and may represent a later ontogenetic stage of the taxon.
Chuanqilong was a medium-sized ankylosaur, with an estimated length of 4.5 metres (14.8 feet), although it has been suggested that it would have been larger due to the immature age of the type specimen. It had a triangular skull and a neck that was protected by bands of osteoderms known as cervical half rings. The rest of the body was covered in osteoderms and ossicles of various shapes and sizes. Unlike derived ankylosaurids, the end of its tail lacked a club. Like other ankylosaurids, it was quadrupedal with robust forelimbs and hindlimbs.
A nearly complete skeleton was collected by local farmers from a single quarry in the Liaoning Province, China. The skeleton was recovered from the Jiufotang Formation which dates to the late Barremian to Aptian stages of the Early Cretaceous period, 122.0 to 118.9 Ma. The specimen was named and described in 2014 by Fenglu Han, Wenjie Zheng, Dongyu Hu, Xing Xu, and Paul M. Barrett. The holotype specimen, CJPM V001, consists of a nearly complete skull and skeleton, with only the distal portion of the caudal series missing, and represents a juvenile individual. The authors noted that the specimen was at a more advanced ontogenetic stage than the specimens of the sympatric Liaoningosaurus based on the larger size of the type specimen, the size of the orbit and the tooth count. The specimen is preserved two-dimensionally, with only the ventral side being visible. Most of the skull is compressed dorsoventrally and most of the vertebral column is disarticulated, while the limbs are preserved in articulation. The type specimen is currently housed at the Chaoyang Jizantang Paleontological Museum, while a cast of the specimen (IVPP FV 1978) is housed at the Institute of Vertebrate Paleontology and Paleoanthropology. [1]
The generic name, Chuanqilong, is derived from the Chinese words "Chuanqi" (legendary), in reference to the abundance of fossils of western Liaoning, and "long" (dragon). The specific name, chaoyangensis, refers to the broader geographical area which encompasses the type locality. [1]
In 2014, the impressions of a scapulocoracoid and humerus belonging to an indeterminate ankylosaur with an estimated body length of 6.0-8.6 metres (19.7-18.2 feet) were described from the Jiufotang Formation and, at the time, was the first ankylosaur described from the formation. [2] A Canadian Society of Vertebrate Palaeontology abstract book that was published in 2019 mentioned that the type and only known specimen of Chuanqilong actually represented an adult individual, in contrast to the interpretation of Han et al. (2014), and may have been Liaoningosaurus at a different and later ontogenetic stage. [3]
Han et al. (2014) gave Chuanqilong an estimated length of 4.5 metres (14.8 feet). However, the authors suggested that it could have reached larger sizes as the type specimen represents a juvenile individual. [1]
The describing authors indicated two distinguishing traits. Both of these are autapomorphies, unique derived characters. The quadrate has a glenoid fossa that is at the same level as the dentary tooth row. The distally tapering ischium is constricted at midshaft length. Other distinguishing traits include the presence of a long retroarticular process, the presence of a lacrimal that is slender and wedge-like, a ratio of humerus to femur length of 0.88, the width of the proximal end of the humerus is half of the length of the humeral shaft, and the presence of subtriangular unguals. [1]
In ventral view, the skull is triangular. The maxilla has a buccal with a notched margin that is shallow and flattened, while an antorbital fenestra is present in the caudodorsal region. A slender, wedge-shaped lacrimal forms the rostral margin of the orbit and a long supraorbital contacts the lacrimal rostroventrally. A bone which might be composed of the squamosal and the postorbital has a subrectangular outline and grooves that are subparallel. The left quadrate has a rectangular head and is straight, with the shaft forming a wide and shallow depression underneath the quadrate head. Unlike nodosaurids, the quadrate isn't fused with the squamosal. The pterygoid process has a transversely expanded ventral end which is composed of two mandibular condyles, and has an outline that is subrectangular. As in most other ankylosaurs, the medial condyle is wider across and extends further towards the underside than the lateral condyle. As in most ankylosaurs, with the exception of Ankylosaurus , the left maxilla has at least 20 alveoli. The rostral maxillary teeth that are preserved are smaller than the caudal teeth, with their crowns being as tall as they are wide and their bases being swollen with a weak cingulum. The teeth lack crescentic cingula. A rostral maxillary tooth crown has small denticles and cusps present. Some of the teeth have denticles that taper with a round cross-section at the base. [1]
The mandible is similar to that of other basal ankylosaurids as it is long and shallow. However, it lacks an osteoderm on the underside margin unlike other basal ankylosaurids. The absence of the osteoderm might be a result of incomplete preservation as it may not have been fused to the mandibular bone due to the immature age of the holotype. If an osteoderm was presents, it might have been restricted to the sides corner of the mandible. The dentary tooth row is not as strongly sinusoidal as those of derived ankylosaurs and is straight. The dentary has at least 20 alveoli present, with most of the teeth missing. The teeth preserved are similar to the maxillary teeth. The symphysis of the right dentary is downturned slightly and the cross-section is sub-triangular. As in nodosaurids, the coronoid eminence projects above the level of the dentary tooth row. Below the coronoid eminence is the large adductor fossa. The retroarticular process is long and slender, while the articular is small. The glenoid fossa is unlike that of other ankylosaurs as it is situated at the same level as the dentary tooth row. [1]
The centra of the cervical and dorsal vertebrae are spool-like. The cervical centra are shorter than they are wide, while the dorsal centra are longer than tall. and the sacral centra are wider than it is long. All of the centra of the dorsal vertebrae lack a ventral keel. The sacral ribs have a dumbbell-shaped outline and are robust. Present on the caudal vertebrae are deep longitudinal grooves. The centrum of a middle caudal vertebra has a square outline in lateral view. The upper part of the sides of the centrum possesses a transverse process that has been reduced to a small nodular process. The neural spines have a arc-shaped outline and are elongated. The facets of the prezygapophyseal face craniomedially, while the postzygapophyses face caudolaterally. The caudal vertebrae have neural spines that join together with postzygapophyses, as to form a caudal process which ends cranial to the midpoint of the following vertebrae. The reduction of the size of the postzygapophyses coincides with the reduction of the prezygapophyses. Unlike other ankylosaurids, Chuanqilong lacked a tail club as it lacks the modified handle-like vertebrae in the distal portion of the tail. [1] [4]
The coracoid is not co-ossified with the scapula, which might represent an ontogenetic trait as it is also known in other juvenile ankylosaur specimens. The scapula blade has a rhomboid-like outline, with a dorsal margin that is straight and a ventral margin that is concave. The narrowest point of the scapular blade is towards the head of the glenoid fossa. The ventral edge of the scapula lacks a distinct enthesis, which may also represent an ontogenetic trait. The glenoid fossa has an oval outline and is large. The humerus is short, with a large deltopectoral crest. The proximal end of the femur has a width that is much greater than the width of the distal end. The radial condyle is more prominent than the medial ulna condyle, while the lateral epicondylar ridge is underdeveloped. The ulna has a wedge-shaped olecranon process, as in other immature ankylosaur specimens and may represent an ontogenetic characteristic. The radius is slender and rod-like, with a distal end that is wider transversely than the proximal end of the radius. Only the left manus is known, which consists of four metacarpals that are all slender in appearance. Out of all the metacarpals, metacarpal III is the longest while metacarpal IV is the shorter. The other metacarpals are sub-equal in length. The most robust metacarpal is metacarpal I, while metacarpals II and IV are the slenderest. The distal and proximal ends if all the metacarpals are expanded. The ungual phalanges have a triangular outline with a sharp point, while the ventral surfaces are flattened. [1]
The preacetabular process of the ilium is long and is rotated towards the middle, while the postacetabular process is rotated in apposition. The preacetabular process diverges sideways from the vertebral column and has a straight side margin. The postacetabular process has a subtriangular outline and is shorter than the acetabulum. The pubic peduncle has a profile that is sub-rounded and developed, while the ischial peduncle is undeveloped. The ischium is long, lacks an obturator process and has a slender shaft that curves slightly towards the underside. The mid-shaft region of the ischium is narrow and widens towards the distal end before tapering further distally. The ischium has a proximal end that is straight in side view, unlike the convex and fan-like ischium of Ankylosaurus and the concave proximal ischia of Struthiosaurus . [1]
As typical with other ankylosaurs, the femur is both robust and straight. The femoral head forms an articular surface that is circular. The femur possesses both the cranial and greater trochanters, which are separated from the femoral head by a tightening. The cranial trochanter is separated from the greater trochanter, which is seen in juvenile ankylosaur specimens but not in most adult ankylosaurs. However, this may rather represent a plesiomorphic trait of ankylosaurids, as well as a trait under ontogenetic control in some ankylosaurs, due to the cranial trochanter being also present in some nodosaurids. Present on the femur is a shallow cranial intercondylar fossa. Chuanqilong has a similar ratio of humerus to femur length to Ankylosaurus, but lower than that of other juvenile ankylosaur specimens and Hungarosaurus . The tibia is shorter than the femur and robust, with the proximal end having a transverse expansion that is weaker then that of the distal end of the tibia. Slightly shorter than the tibia is the fibula, which is slender and has a shaft that is oval in cross-section, as well as being relatively equal in size. The right foot preserves metatarsals II, III, and IV in articulation. The longest and most robust metatarsal is metatarsal III, while metatarsals II and IV are both sub-equal in length. All of the preserved metatarsals have proximal and distal ends that are expanded. The unguals have a sub-triangular outline with distal ends that are sub-rounded and are similar to that of Dyoplosaurus . [1]
The only preserved cervical half ring of Chuanqilong consists of a connecting band that is fused into a single plate, but is compressed towards the dorsal and ventral sides and is also segmented into four sections. Of these sections, the right three have a subrectangular outline and are arched upwards, while the left section has a subtriangular profile and tapers caudolaterally. The shoulder region preserves two osteoderm plates that are large, flat, thickened and have a subrectangular outline. The largest of these osteoderm plates is twice the length of the other and are both similar to the osteoderms of cervical half ring but may also represent separate cervical osteoderm plates. Between the proximal end of the left ulna and radius is a small triangular osteoderm that has a wide base and tapers distally. Present near the left ischium is an oval osteoderm that is sharply keeled along the midline. Preserved over the entirety of the body are a diverse range of osteoderms and ossicles that are small and irregular. [1]
Han et al. (2014) originally found Chuanqilong to be a basal ankylosaurid that was sister taxon to Liaoningosaurus . The authors noted that only two unambiguous synapomorphies supported its close relationship to Liaoningosaurus, which are the presence of an antorbital fossa and a ventrally oriented scapula glenoid. The authors also noted that, although both taxa are represented by juvenile specimens and are sister taxa, Chuanqilong can be differentiated from Liaoningosaurus based on a number of characteristics such as the differences in the metatarsus to metacarpus length ratio and the morphology of the cheek tooth crown. [1] Cladistic analyses conducted by Arbour & Currie (2015) recovered Chuanqilong as either being within a polytomy with other basal ankylosaurids or as sister taxon to Cedarpelta , a position also recovered by Arbour et al. (2016). [5] [6] Analyses conducted by Arbour & Evans (2017), Zheng et al. (2018) and Park et al. (2019) similarly placed Chuanqilong within a polytomy with other basal ankylosaurids, although the inclusion of certain taxa such as Aletopelta within the internal node varied. [7] [8] [9] Rivera-Sylva et al. (2018) also recovered it within a polytomy in a strict consensus tree, but it was also recovered it as sister taxon to Cedarpelta in a 50% majority rule tree. Contrary to other analyses, Frauenfelder et al. (2022) found Chuanqilong to be within a clade including Liaoningosaurus and Cedarpelta outside of Ankylosauridae and Nodosauridae. [10] In 2019, an abstract suggested the possibility that Chuanqilong and Liaoningosaurus may represent the same species but at different ontogenetic stages. [3]
Below is a reproduced phylogenetic analysis from Arbour & Currie (2015). [5]
Ankylosauridae |
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The remains of Chuanqilong were uncovered from the Jiufotang Formation of the Jehol Group. The formation is composed of mudstones, siltstones, shales, sandstones and tuffs, and overlies the Yixian Formation. Recent secondary ion mass spectrometry (SIMS) zircon U-Pb analyses suggest that the formation dates to the late Barremian to Aptian stages of the Early Cretaceous, ca. 122.0–118.9 Ma. [11] Both the Yixian and Jiufotang Formations represent freshwater lacustrine environments that lacked rivers as well as many other variable features of freshwater settings, and would have fluctuated seasonally between semi-arid and mesic conditions. The Jiufotang Formation experienced infrequent volcanic activity, while the younger Yixian Formation had more frequent activity. A combination of regional volcanism and the presence of many shallow lakes allowed the exceptional preservation of fossils and the preservation of integument impressions, cartilage and keratin. [12]
A variety of forms of Euornithines (such as Mengciusornis , [13] Piscivoravis , [14] Parahongshanornis , [15] and Yanornis [16] ) and Enantiornithines (such as Cuspirostrisornis , [17] Longipteryx , [18] Rapaxavis , [19] Sinornis , [20] and Yuanchuavis [21] ) are present in the Jiufotang Formation. Numerous pterosaurs are also known from the formation including the chaoyangopterids Chaoyangopterus , [22] Eoazhdarcho , [23] Jidapterus [24] and Shenzhoupterus , [25] the ctenochasmatid Forfexopterus , [26] the anhanguerids Guidraco [27] and Liaoningopterus, [22] the lonchodraconid Ikrandraco , [28] the istiodactyliforms Hongshanopterus , [29] Liaoxipterus , [30] Linlongopterus [31] and Nurhachius , [32] [33] the tapejarid Sinopterus , [34] the anurognathid Vesperopterylus [35] and the indeterminate pterodactyloid Pangupterus . [36] Other fauna present include the jeholornithiforms Jeholornis [37] and Kompsornis , [38] the omnivoropterygids Omnivoropteryx [39] and Sapeornis , [40] the oviraptorosaur Similicaudipteryx , the dromaeosaurid Microraptor , [41] the tyrannosauroid Sinotyrannus , [42] the ceratopsian Psittacosaurus , the mammaliamorphs Fossiomanus [43] and Liaoconodon , [44] and the choristoderes Philydrosaurus , [45] Ikechosaurus [46] and Liaoxisaurus . [47]
Crichtonsaurus is a genus of herbivorous ankylosaurid dinosaur that lived during the Late Cretaceous in what is now China. It was named after Michael Crichton, the author of the dinosaur novel Jurassic Park. A sister taxon was discovered, C. benxiensis, which is now identified as a separate genus.
Ankylosauridae is a family of armored dinosaurs within Ankylosauria, and is the sister group to Nodosauridae. The oldest known Ankylosaurids date to around 122 million years ago and went extinct 66 million years ago during the Cretaceous–Paleogene extinction event. These animals were mainly herbivorous and were obligate quadrupeds, with leaf-shaped teeth and robust, scute-covered bodies. Ankylosaurids possess a distinctly domed and short snout, wedge-shaped osteoderms on their skull, scutes along their torso, and a tail club.
Aletopelta is a monospecific genus of basal ankylosaurid dinosaur from Southern California that lived during the Late Cretaceous in what is now the Point Loma Formation. The type and only species, Aletopelta coombsi, is known from a partial skeleton preserving osteoderms. It was originally described in 1996 by W. P. Coombs, Jr. and T.A. Deméré before being named in 2001 by Tracy Ford and James Kirkland. Aletopelta has an estimated size of 5 metres and weight of 2 tonnes. The holotype formed a miniature reef and was scavenged upon by invertebrates and sharks.
Dyoplosaurus is a monospecific genus of ankylosaurid dinosaur from Alberta that lived during the Late Cretaceous in what is now the Dinosaur Park Formation. Dyoplosaurus represents a close relative of Scolosaurus and Anodontosaurus, two ankylosaurids known from the Horseshoe Canyon and Dinosaur Park Formation.
Texasetes is a genus of ankylosaurian dinosaurs from the late Lower Cretaceous of North America. This poorly known genus has been recovered from the Paw Paw Formation near Haslet, Tarrant County, Texas, which has also produced the nodosaurid ankylosaur Pawpawsaurus.
Cedarpelta is an extinct genus of basal ankylosaurid dinosaur from Utah that lived during the Late Cretaceous period in what is now the Mussentuchit Member of the Cedar Mountain Formation. The type and only species, Cedarpelta bilbeyhallorum, is known from multiple specimens including partial skulls and postcranial material. It was named in 2001 by Kenneth Carpenter, James Kirkland, Don Burge, and John Bird. Cedarpelta has an estimated length of 7 metres and weight of 5 tonnes (11,023 lbs). The skull of Cedarpelta lacks extensive cranial ornamentation and is one of the only known ankylosaurs with individual skull bones that are not completely fused together.
Mymoorapelta is a nodosaurid ankylosaur from the Late Jurassic Morrison Formation of western Colorado and central Utah, USA. The animal is known from a single species, Mymoorapelta maysi, and few specimens are known. The most complete specimen is the holotype individual from the Mygatt-Moore Quarry, which includes osteoderms, a partial skull, vertebrae, and other bones. It was initially described by James Kirkland and Kenneth Carpenter in 1994. Along with Gargoyleosaurus, it is one of the earliest known nodosaurids.
Tianzhenosaurus is a monospecific genus of ankylosaurid dinosaur from the Shanxi Province that lived during the Late Cretaceous in what is now the Huiquanpu Formation. Tianzhenosaurus may represent a junior synonym of Saichania, an ankylosaurine known from the Barun Goyot and Nemegt Formation.
Liaoningosaurus is an unusual genus of basal ankylosaurid dinosaur from the Liaoning Province, China that lived during the Early Cretaceous in what is now the Yixian and Jiufotang Formation. The type and only species, Liaoningosaurus paradoxus, is known from more than 20 specimens, with some representing juveniles. It was named in 2001 by Xu, Wang and You.
Shanxia is a monospecific genus of ankylosaurid dinosaur from the Shanxi Province that lived during the Late Cretaceous in what is now the Huiquanpu Formation. Shanxia may possibly represent a junior synonym of Tianzhenosaurus, an ankylosaurine also known from the Huiquanpu Formation of China.
Zhongyuansaurus is a monospecific genus of ankylosaurid dinosaur from Henan that lived during the Early Cretaceous in what is now the Haoling Formation. Zhongyuansaurus is possibly a junior synonym of Gobisaurus, a basal ankylosaurid from the Ulansuhai Formation of Inner Mongolia.
The Jehol Biota includes all the living organisms – the ecosystem – of northeastern China between 133 and 120 million years ago. This is the Lower Cretaceous ecosystem which left fossils in the Yixian Formation and Jiufotang Formation. These deposits are composed of layers of tephra and sediment. It is also believed to have left fossils in the Sinuiju series of North Korea. The ecosystem in the Lower Cretaceous was dominated by wetlands and numerous lakes. Rainfall was seasonal, alternating between semiarid and mesic conditions. The climate was temperate. The Jehol ecosystem was interrupted periodically by ash eruptions from volcanoes to the west. The word "Jehol" is a historical transcription of the former Rehe Province.
The Jiufotang Formation is an Early Cretaceous geological formation in Chaoyang, Liaoning which has yielded fossils of feathered dinosaurs, primitive birds, pterosaurs, and other organisms. It is a member of the Jehol group. The exact age of the Jiufotang has been debated for years, with estimates ranging from the Late Jurassic to the Early Cretaceous. New uranium-lead dates reveal the formation is deposited in the Aptian stage of the Early Cretaceous. Fossils of Microraptor and Jeholornis are from the Jiufotang.
Peloroplites is a monospecific genus of nodosaurid dinosaur from Utah that lived during the Late Cretaceous in what is now the Mussentuchit Member of the Cedar Mountain Formation. The type and only species, Peloroplites cedrimontanus, is known from a partial skull and postcranial skeleton. It was named in 2008 by Kenneth Carpenter and colleagues. Peloroplites was 6 metres long and weighed 2 tonnes, making it one of the largest known nodosaurids, and came from a time when ankylosaurids and nodosaurids were attaining large sizes.
Minotaurasaurus is a monospecific genus of ankylosaurid dinosaur that lived in Mongolia during the Late Cretaceous in what is now the Djadochta Formation. The type and only species, Minotaurasaurus ramachandrani, is known from two skulls, a cervical vertebra and a cervical half ring. It was named and described in 2009 by Clifford Miles and Clark Miles. The first fossils of Minotaurasaurus were illegally exported out of Mongolia.It has been suggested to be a synonym of Tarchia but more recent publications consider it as a distinct genus.
Ahshislepelta is a monospecific genus of ankylosaur dinosaur from New Mexico that lived during the Late Cretaceous in what is now the Hunter Wash Member of the Kirtland Formation. The type and only species, Ahshislepelta minor, is known only from an incomplete postcranial skeleton of a small subadult or adult individual. It was named in 2011 by Michael Burns and Robert M. Sullivan. Based on the size of the humerus, Ahshislepelta is larger than Pinacosaurus mephistocephalus but smaller than Talarurus and Pinacosaurus grangeri.
Dongyangopelta is an monospecific genus of nodosaurid dinosaur that lived in China during the Early to Late Cretaceous period in what is now the Chaochuan Formation. The type and only known species, Dongyangopelta yangyanensis, is known from a partial postcranial skeleton preserving osteoderms and ossified tendons. It was named in 2013 by Rongjun Chen, Wenjie Zheng, Yoichi Azuma, Masateru Shibata, Tianling Lou, Qiang Jin and Xinsheng Jin. Dongyangopelta represents one of the only nodosaurids known from Asia, along with Taohelong and Sauroplites.
Europelta is a monospecific genus of nodosaurid dinosaur from Spain that lived during the Early Cretaceous in what is now the lower Escucha Formation of the Teruel Province. The type and only species, Europelta carbonensis, is known from two associated partial skeletons, and represents the most complete ankylosaur known from Europe. Europelta was named in 2013 by James I. Kirkland and colleagues. Europelta has an estimated length of 5 metres and weight of 1.3 tonnes, making it the largest member of the clade Struthiosaurini.
This timeline of ankylosaur research is a chronological listing of events in the history of paleontology focused on the ankylosaurs, quadrupedal herbivorous dinosaurs who were protected by a covering bony plates and spikes and sometimes by a clubbed tail. Although formally trained scientists did not begin documenting ankylosaur fossils until the early 19th century, Native Americans had a long history of contact with these remains, which were generally interpreted through a mythological lens. The Delaware people have stories about smoking the bones of ancient monsters in a magic ritual to have wishes granted and ankylosaur fossils are among the local fossils that may have been used like this. The Native Americans of the modern southwestern United States tell stories about an armored monster named Yeitso that may have been influenced by local ankylosaur fossils. Likewise, ankylosaur remains are among the dinosaur bones found along the Red Deer River of Alberta, Canada where the Piegan people believe that the Grandfather of the Buffalo once lived.
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.
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