Showing posts with label Troodontids. Show all posts
Showing posts with label Troodontids. Show all posts

Wednesday, 7 December 2022

Fossil eggshells from the Early Cretaceous Okurodani Formation of Gifu Prefecture, Japan.

The past three decades have seen the discovery of a large quantity of fossil eggs from several Lower Cretaceous deposits in Japan, notably the Yezo Group of Hokkaido, the Kuwajima Formation of Ishikawa Prefecture, and the Ohyamashimo Formation in Hyōgo Prefecture. These include eggs which are thought to have come from Ornithopod and Theropod Dinosaurs (including Oviraptosaurs, Troodontids, and Birds). These findings add to the known palaeobiodiversity of these areas, by indicating the presence of groups not known from the skeltal fossil record. However, the majority are of Aptian or Albian age (121.4-100.5 million years old), with earlier examples being much rarer.

The Okurodani Formation outcrops in the Shokawa area of northwestern Gifu Prefecture, and is considered to be of Hauterivian age (i.e. between 132.9 and 129.4 million years old). This formation has produced a variety of Vertebrate remains, including Dinosaurs, aquatic Tetrapods and Fish, as well as a number of fragmentary egg pieces, which have been assumed to have been of Dinosaurian origin, but never formally investigated.

In a paper published in the journal Historical Biology on 24 November 2022, Rina Uematsu of the Graduate School of Science and Technology at the University of TsukubaKohei Tanaka of the Faculty of Life and Environmental Sciences at the University of Tsukuba, Shohei Kozu of the Gifu Prefectural Museum, Shinji Isaji of the Natural History Museum and Institute of Chiba, and Shizuo Shimojima of Takayama City, describe the known egg material from the Okurodani Formation, and discuss the implications this has for the known biodiversity of the environment which produced these strata.

All the fossils examined in the study were collected between 1988 and 2009 by Shizuo Shimojima, Masatoshi Okura and Satoru Sakamoto, from the Okurodani Formation, a 220 m thick sequence of shale, alternating sandstone and mudstone, and sandstone beds, which forms part of the Itoshiro Subgroup of the Middle Jurassic to Lower Cretaceous Tetori Group, which has been dated to between 133 and 129 million years old, based upon uranium-lead dates obtained from layers of volcanic tuff within the formation.

Map of the eggshell locality. (A) Distribution of the Tetori Group in Japan formed of three subgroups. (B) Stratigraphic position of the Okurodani Formation in the Shokawa area. (C) Detail of the boxed area in (A), showing the distribution and the stratigraphic sequence of the Okurodani Formation with the locations where eggshell materials were collected. GPM-Fo-1923, 09/Cr/89/01 and 09/Cr/88/07 were found in debris of fallen rocks and their location is not specified in the stratigraphy. Uematsu et al. (2022).

Sevem fragments of eggshell and two eggshell impressions were found within black mudstone layers within the Okurodani Formation. These mudstone layers are also rich in Plant fossils and freshwater Molluscs, and are interpretted as having been laid down in a network of stagnant pools or oxbow lakes within a floodplain environment. Vertebrate remains, predominantly Fish scales and Turtle shells, but also including Frogs, small Lizards, and Choristoderes (Crocodile-like Diapsids of uncertain affinities) are typically preserved in three dimensions (i.e. not compressed),  which implies rapid burial with minimal movement. Dinosaur fossils are rare in these layers, but the teeth of Ornithopods, Sauropods, and Verociraptorines have been found, as well as the tarsometatarsus of an Enantiornithine Bird.

The first two eggshell fragments discussed, GPM-Fo-1923 and 09/Cr/89/01, are assigned to the Oofamily Testudoolithidae (i.e. Turtle Eggs). These fragments are approximately 5 x 6 mm and 3 x 3 mm, respectively, and are assumed to have come from the same egg, based upon cross-sections of the joint and the overall  shape of the fragments when jointed. However their precise origin is unclear, because they were collected by Masatoshi Okura, who has since passed away, and are now housed in separate museums. The outer surfaces of both shells are strongly abraded and show nodular patterns composed of tightly packed shell units. Based upon the curvature of the eggshell, the original egg would have been about 22 mm in diameter.

Eggshell assigned to Testudoolithidae. (GPM-Fo-1923). (A) Nodular outer surface with exposed shell units. (B) Radial thin section under normal light, showing discrete shell units (bracket), tubular pore canals (white arrowheads) and cratered bases (black arrowhead). The shell appears two-layered with an undulating boundary (arrow). (C) The same view as (B) under polarised light, exhibiting irregular extinction patterns. (D) Radial view, scanning electron microscope, showing discrete shell units (bracket) with ill-preserved ultrastructure. Uematsu et al. (2022).

These shells show two separate layers, separated by an undulating horizontal boundary. In the upper layer, needle-like crystals radiate outward from the boundary. Although less prominent, such acicular crystals are also found in the lower layer; the crystals develop concentrically from the organic cores, making the basal parts of the shell units rounded in shape. Under polarised light, the eggshell exhibits irregular extinction patterns. 

Turtle eggs typically have only a single layer, so the structure of the these eggshells, with two distinct layers, each with a different type of crystals, is distinctly unTestudine. Apparently double-layered Turtle eggshells can be produced taphonomically, by when two shell fragments happen to come to rest with one sitting inside the other, or as a result of a pathology - gravid female Turtles, suffering from some king of environmental stress, can retain eggs instead of laying them, depositing additional layers of minerals on the surface of the egg during the process. Neither of these appears to be the case in this instance, rather the eggs appear to have been altered diagenetically, with the outer portion of the shell having been recrystalised as a result of contact with external chemistry.

Based upon the morphology of these eggshell fragments, it is estimated that they were laid by a small Cryptodiran Turtle, with a carapace length of less than 200 mm.

The next five specimens, GPM-Fo-1294, 1295, 1296, 1297, and 1298 are placed within the Oofamily Prismatoolithidae, which is typified by a two-layered structure and an ornamented shell surface. They are assigned to a new oospecies, with GPM-Fo-1925 as the holotype, and given the name Ramoprismatoolithus okurai, where 'Ramoprismatoolithus' derives from 'Ramo-' from the Latin 'ramus', meaning branch, plus '-prismatoolithus', from the oofamily name, in reference to the reticulate ridges on the other surface of the eggshell, and 'okurai', honours the late Masatoshi Okura who pioneered the discovery of fossil eggshells and other Vertebrate remains in Shokawa.

All of these specimens are fragmentary; no intact examples of this new oospecies are known. The outer surface of these shells is distinctly sculpted, with low ridges arranged in elaborate reticulated patterns. The shells range from 0.31 to 0.61 mm in thickness, with the average being 0.46 mm. Seen under a scanning electron microscope, a near-vertical, unbranching, pore canal could be observed, increasing slightly in width towards the surface of the egg.

Ramoprismatoolithus. (A), (B) Eggshell outer surfaces showing the well-sculpted reticulation: (A) holotype: GPM-Fo-1925 and (B) a cast of GPM-Fo-1924 made of  silicone rubber. (C) Radial thin section under normal light, showing a mammillary layer (ML) and a prismatic layer (PL) with a gradual boundary (horizontal bar on the left side) (holotype: GPM-Fo-1925). (D) the same view as (C) under PLM, showing columnar extinction patterns. (E)–(G) Radial view under Scanning Electron Microscope (holotype: GPM-Fo-1925), displaying (E) ML and PL, (F) numerous vesicles (arrowhead) over the eggshell and (G) acicular crystals at the base of mammillae. (H) Straight pore canal under Scanning Electron Microscope (GPM￾Fo-1928). Uematsu et al. (2022).

These eggshells show two layers, which appears to be an original feature rather than something produced by diagenetic alteration, with a lower mammillary layer (the inner layer of many eggs, which is made up of small calcium carbonate crystals, which are easily disolved and provide a source of calcium for the growing embryo) and the upper prismatic layer (made up of larger crystals, which provides structural strength to the egg) observable. These are separated by a gradual boundary. The mammillary layer makes up about one fifth to one sixth of the shell's thickness, and is comprised of  acicular crystals radiating from what were presumably organic cores. The base of this layer is abraded, probably due to absorption of calcium by the growing embryo. The prismatic layer is made up of narrow, columnular crystals, visible under polarised light. Vesicles can be seen in this layer under the scanning electron microscope.

Based upon the thickness of the shell fragments, the original Ramoprismatoolithus okurai eggs are calculated to have had an average mass of 99.39 g, which assuming an egg twice as long as it is wide, would give an original size of about 57 x 133 mm.

Prismatoolithid eggs are generally accepted to have been laid by Troodontid Dinosaurs, as intact eggs assigned to the oofamily have been found with Troodontid embryos inside. However, it has been suggested that some eggs assigned to this oofamily might have been laid by early Birds.

The small estimated size of the Ramoprismatoolithus okurai eggs leads Uematsu et al. to conclude the Animal which laid them weighed somewhere between twelve and seventeen kilograms, small for a Theropod Dinosaur, but not implausible for a non-Avian Maniraptoran.

The final two specimens described are GPM-Fo-1929, an impression of part of an outer eggshell surface measuring 6 × 7 mm, and 09/Cr/88/07, a possible impression of part of an inner eggshell surface, measuring 2 x 2 mm. Neither of these specimens preserves any of the original eggshell material. The outer surface impression GPM-Fo-1929 bears a strong resemblance to the outer surface of the Ramoprismatoolithus okurai egg fragments, with reticulate ornamentation and the remains of several pore openings. The inner shell fragment impression, 09/Cr/88/07, is smooth, with no discerning features which would allow it to be associated with any known egg fossil.

Indeterminate eggshell impressions. (A) Outer surface impression (GPM-Fo-1929). (B) Cast of (A) made of silicone rubber, showing reticulate ornamentation similar to Ramoprismatoolithus and remains of pore openings (arrowheads) between the ridges. (C) Inner? surface impression with a smooth appearance (09/Cr/88/07). Uematsu et al. (2022).

The specimens described by Uematsu et al. are the oldest known fossil eggshells from Japan, and provide additional information on biodiversity within the Early Cretaceous Tetori Group, within which skeletal material is scarce, demonstrating that Turtles and small Dinosaurs were nesting in the area. 

The eggs assigned to Ramoprismatoolithus okurai are likely to have been laid by a Troodontid, or closely related Maniraptoran Theropod. Okurodani Formation yields teeth of possible Velociraptorinae, and other strata within the Tetori Group (likely to be roughly co-eval, but laid down in different environments within the same landscape) have produced possible Oviraptorosauria and Dromaeosauridae, as well as the Therizinosaur-related Fukuivenator paradoxus. However, all of these groups are known to produce non-prismatic shells with microstructures unlike that of the Oofamily Prismatoolithidae. This strongly suggests that the Ramoprismatoolithus okurai eggs were produced by a small Maniraptoran Theropod not represented in the skeletal fossil record of the Tetori Group. 

Troodontids, and basal Paravians (the group that includes Troodontids, Birds, and Dromaeosaurs) in general are scarce in Early Cretaceous deposits, both as skeletal and egg remains. Examples are known from the US, Spain, and China, and all Early Cretaceous small non-Avian Theropods known from East Asia come from two formations in northeastern China, the Yixian and Huajiying. Thus the discovery of the Ramoprismatoolithus okurai eggs in Japan is a significant contribution to our understanding of the distribution of mall non-Avian Theropods from the early Early Cretaceous of East Asia.

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Tuesday, 2 August 2022

Three-dimensionally preserved Dinosaur remains from a new Jehol Biota outcrop in Inner Mongolia.

The Jehol Biota produces a wide range of exquisitely preserved Early Cretaceous fossils from locations across Liaoning, Inner Mongolia, and Hebei provinces in northeastern China. However, in almost all cases these are two-dimensionally preserved (i.e. flattened), with only a single site, an outcrop of the the Lujiatun Unit of the Yixian Formation in western Liaoning, producing fossils in three dimensions. The fossils from this location are predominantly Dinosaurs, with some Lizards and Mammals, and show signs of representing an area with an area with a different faunal composition and ecology to the rest of the Jehol Biota, as well as having a different taphonomy (mode of preservation).

In a paper published in the journal Acta Palaeontologica Polonica on 20 June 2022, Honggang Zhang of the College of Earth Science and Engineering, and Paleontological Institute at Shandong University of Science & Technology, Dongxiang Yu, also of the College of Earth Science and Engineering at Shandong University of Science & Technology, Yuhui Feng, also of the Paleontological Institute at Shandong University of Science & Technology, Rui Pei of the Key Laboratory of Evolutionary Systematics of Vertebrates at the Institute of Vertebrate Paleontology and Paleoanthropology of the Chinese Academy of Sciences, and Chang-Fu Zhou, again of the College of Earth Science and Engineering at Shandong University of Science & Technology, describe a second outcrop producing three-dimensionally preserved fossils from the Jehol Biota, this time located in the Ningcheng Basin of Inner Mongolia.

The new outcrop, at a site called Xidayingzi in Ningcheng County, comprises an outcrop of interbedded volcanic and sedimentary rocks about 80 m thick. The volcanic rocks here are predominantly basaltic andesites, rhyolitic breccia lavas and andesitic tuffs, while the sedimentary units are gravel-rich siltstones, sandstones, and conglomerates, all containing volcanically derived material.

Map of the Inner Mongolia, Liaoning and Hebei (A) showing location of the Xidayingzi site and the outcrops of the Lujiatun Unit of the Yixian Formation of the Jehol Biota in Beipiao, western Liaoning Province. Stratigraphic column (B) and corresponding photographic image (C) of the Early Cretaceous Xidayingzi site. Zhang et al. (2022).

Initial investigations at this site uncovered the remains of Dinosaurs from four different groups, plus Lizard and Mammal remains, all preserved in three dimensions and many in a semi-articulated state, although most material is individual bones.

Fossils found in the Xidayingzi site from the Early Cretaceous Ningcheng Basin, Inner Mongolia. (A) Sinovenator-like Troodontid Dinosaur (SDUST-V1062), the left pes is exposed in medial view. (B) Ceratopsian Dinosaur Psittacosaurus sp. (PMOL-AD00163), the maxilary teeth are loosely arranged and exposed in lateral view. (C) Neornithischian Dinosaur Jeholosaurus sp. (SDUST-V1063), the scapulocoracoid, humerus, ulna, and radius in lateral view. (D) Euhelopus-like Sauropod (SDUST-V1064), digital image of the tooth crown in medial view. (E) Indeterminated Lizard (PMOLAR00268), digital image of the fragmentary mandible in lingual view. (F) Symmetrodont-like Mammal (PMOL-AM00036), digital image of the mandible in lingual view. Zhang et al. (2022).

The most notable specimen from the site (SDUST-V1062) is the articulated post-cranial skeleton of a Troodontid Dinosaur, possibly a specimen of Sinovenator; the specimen resembles Sinovenator changii in most regards, but differs in having having a round anterior margin of the preacetabular process of the ilium and a moderately developed ambiens process of the pubis, and may therefore represent a second species in the genus.

Three Sauropod teeth were found at the site, two of them well preserved and similar to those of Euhelopus, a Titanosauriform of similar age to the Jehol Biota, but not previously reported from there.

Eight Neornithischian Dinosaur fossils were found at the site, with four being semi-articulated partial postcranial skeletons. These all resemble  Jeholosaurus shangyuanensis, a small Neornithischian previously only known from the Lujiatun Unit of the Jehol Biota.

Six specimens of Ceratopsian Dinosaurs were found, although these were rather fragmentary in nature. All appear similar to the early-diverging Psittacosaurus, often used as an index fossil for the Lower Cretaceous in East Asia, and common in the Jehol Biota. Curiously, the maxillary teeth of the new specimens appear to be spaced apart rather than being imbricated as in all other known Psittacosaurs, which may again indicate they belong to a new species.

A single fragment of a Lizard mandible (PMOL-AR00268) was found. This has pleurodont, conical, single-cusped, and closely packed teeth, which, are features common in a range of Mesozoic Lizards, and not helpful diagnostically.

Mammals are also represented by a single mandible (PMOL-AM00036), which has one premolar, five molars, and eight empty alveoli; the molars have acutely-triangulated molar cusps, which allows the specimen to be referred to the Symetrodonts, although this is a polyphyletic assemblage of Mammals, made up of members of different groups which converged on a similar morphology, possibly as a response to some Mesozoic ecological condition.

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Sunday, 4 February 2018

Almas ukhaa: A new species of Troodontid Dinosaur from the Late Cretaceous of Mongolia.

The Troodontids were a group of small-to-medium sized Maniraptoran Theropod Dinosaurs known from the Cretaceous of Asia and North America. They were closely related to the Birds and Dromeosaurs, with the three groups being classified together as the Paraves. They had large brains and large forward pointing eyes, traits that would generally be associated with predatory behaviour, but their dentition implies a more complex story, with several species having small serrated teeth that would be on their own be taken as indicative of a browsing herbivorous diet, with the two together probably indicating some measure of omnivory.

In a paper published in the American Museum Novitates on 15 December 2017, Rui Pei of the Department of Earth Sciences at the University of Hong Kong, and the Division of Paleontology at the American Museum of Natural History, Mark Norell, also of the Division of Paleontology at the American Museum of Natural History, Daniel Barta of the Richard Gilder Graduate School and Division of Paleontology at the American Museum of Natural History, Gabriel Bever, again of the Division of Paleontology at the American Museum of Natural History, and of the Center for Functional Anatomy & Evolution at the Johns Hopkins University School of Medicine, Michael Pittman of the Vertebrate Palaeontology Laboratory at the University of Hong Kong, and Xing Xu of the Institute of Vertebrate Paleontology and Paleoanthropology of the Chinese Academy of Sciences, describe a new species of Troodontid Dinosaur from the Late Cretaceous Djadokhta Formation of Ukhaa Tolgod in the Ömnögovi Province of southern Mongolia.

The new species is named Almas ukhaa, where 'Almas' refers to a Yeti-like creature from Mongolian folklore and 'ukhaa' to the locality where the specimen was found. The species is described from a single specimen comprising a nearly complete skull and partial post-cranial skeleton, probably that of an almost mature sub-adult. The skull is about 82 mm in length, with four premaxilary (upper front) a teeth, a row of 16 maxilary teeth, smaller at the front and lacking serrations, and 23 dentary (lower) teeth, closer packed at the front.

The specimen of Almas ukhaa. Pei et al. (2017).

The specimen was found associated with a number of eggshell fragments, which almost certainly came from a non-Avian Dinosaur, and quite possibly a Troodontid, though it is impossible to say what the actual relationship of these to the specimen is.

See also...

http://sciencythoughts.blogspot.co.uk/2018/01/caihong-juji-new-species-of-paravian.htmlhttp://sciencythoughts.blogspot.co.uk/2017/12/ostromia-crassipes-second-species-of.html
http://sciencythoughts.blogspot.co.uk/2017/06/an-enantiornithine-bird-hatchling.htmlhttp://sciencythoughts.blogspot.co.uk/2016/12/tongtianlong-limosus-new-species-of.html
http://sciencythoughts.blogspot.co.uk/2016/03/fukuivenator-paradoxus-maniraptoran.htmlhttp://sciencythoughts.blogspot.co.uk/2016/02/boreonykus-certekorum-new-species-of.html
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Wednesday, 31 October 2012

The fate of the Sleeping Dragon.

In October 2004 Xing Xu of the Institute of Vertebrate Paleontology & Paleoanthropology at the Chinese Academy of Sciences and Mark Norell of the American Museum of Natural History published a paper in the journal Nature describing a remarkable Early Cretaceous Troodontid Dinosaur, preserved in volcanic ash in what appears to be a sleeping position. The Dinosaur was named Mei long, meaning Sleeping Dragon. It was a 53 cm long animal, preserved with its tail wrapped around it, and its head tucked under one forelimb, in a manner reminiscent of a sleeping Bird.

Mei long, the Sleeping Dragon. Abbreviations: (cev) cervical vertebrae; (cv) caudal vertebrae; (dv) dorsal vertebrae; (fu) furcula; (lac) left astragalus–calcaneum; (lc) left coracoid; (lf) left femur; (lh) left humerus; (li) left ilium; (lm) left manus; (lp) left pubis; (lpe) left pes; (lr) left radius; (ls) left scapula; (lt) left tibia; (lu) left ulna; (pg) pelvic girdle; (rac) right astragalus–calcaneum; (rc) right coracoid; (rf) right femur; (rh) right humerus; (ri) right ilium; (rm) right manus; (rp) right pubis; (rpe) right pes; (rr) right radius; (rs) right scapula; (ru) right ulna; (sk) skull. Scale bar equals 2 cm. Xu & Norell (2004).

A similar position had previously been observed in another small Troodontid, Sinornithoides youngi (Young's Chinese birdy-thing), described in October 1993 by Dale Russell of the North Carolina Museum of Earth Sciences, and Zhi-Ming Dong of the Institute of Vertebrate Paleontology & Paleoanthropology at the Chinese Academy of Sciences, in a paper in the Canadian Journal of Earth Sciences, though this specimen was less complete, making the diagnosis of the 'roosting position' less obvious. Like Mei long this specimen had been buried in this position, this time in wind-blown sand.

Computed tomography scan image of Sinornithoides youngi. D'Urso, Thompson & Earwaker (2000).

In a paper published in the journal Paleobiology in March 2007, Cynthia Marshall Faux of the Department of Paleontology at the Museum of the Rockies and Kevin Padian of the Department of Integrative Biology and Museum of Paleontology at the University of California, Berkeley disputed the sleeping analysis of Mei long and Sinornithoides youngi, suggesting that their position might instead be a reflexive position caused by reflexive curving of the spine due to muscle spasming during asphyxiation, rather than a sleeping pose.

In a paper published in the journal PLoS One on 27 September 2012, a team of scientists led by Chunling Gao of the Dalian Natural History Museum describe the discovery of a second specimen of Mei long, preserved like the first in an apparent roosting position, and discuss the implications of this study.

The new Mei long specimen. Abbreviations: (aofe) antorbital fenestra; (c) cervical vertebra(e) unnumbered; (c6) sixth cervical vertebra; (c7) seventh cervical vertebra; (ca1–ca18) caudal vertebrae (one through eighteen); (co) coracoid; (d) dentary; (dv) dorsal vertebra(e); (f) frontal; (fm) femur; (fl) fibula; (h) humerus; (il) ilium; (l) lacrimal; (mt-II, mt-III), second metatarsal, third metatarsal etc.; (mx) maxilla; (mxfl?) maxillary fenestra; (n?) nasal; (nc) neural canal; (ns) neural spine; (o) orbit; (p) parietal; (pu) pubis; (pmx) premaxilla; (q) quadrate; (r) radius; (s1, s2, etc.) first sacral vertebra, second sacral vertebra etc.; (sa) surangular; (sc) scapula; (sp) fused neural spine of sacrum; (t) tibia; (u?) possible manual ungual; (ul) ulna; (II-2) second phalanx of digit II of pes; (II-3) third phalanx of digit II of pes; (III-1) first phalanx of digit III of pes; (IV-1–
IV-4) first through fourth phalanges of digit IV. Scale bar equals 1 cm. Gao et al. (2012).

Gao et al. observe that in human victims of asphyxiation the fingers are commonly found in a contorted position, and since three specimens of Troodontid Dinosaurs have now been found in an identical position, none of which show any sign of contorted digits, that it is reasonable to assume that the death position of the dinosaurs was not a result of asphyxiation. They do not, however rule out asphyxiation as a cause of death, observing that a number of bodies recovered from Pompeii appear to be sleeping peacefully, from which they conclude it may be possible to asphyxiate in a deep sleep without undergoing reflexive muscle contortions. They suggest that since the Dinosaurs were killed in a way that did not disturb them from their sleeping position (which would certainly be the case if they were interred by a volcanic lahar or similar) then they may have died within burrows, enabling the bodies to be preserved without exposure to weathering elements or the activities of scavengers.


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Monday, 5 March 2012

Dinosaur footprints from the Early Cretaceous of Ganzu Province, China.

The Deinonychosaurs are the group of dinosaurs most closely related to the birds. They are divided into two groups, the Dromaeosaurs (popularly known as 'Raptors') and the Troodontids, which share a common hindlimb morphology, with two digits used to support weight during locomotion, and a third supporting a large, sickle-shaped claw, which was held clear of the ground.

In a forthcoming paper in the journal Acta Paleontologica Polonica, a team of scientists led by Lida Xing of the Department of Biological Sciences at the University of Alberta describe the discovery of a group of tracks made by dinosaurs with two walking toes, in the Liujiaxia Dinosaur National Geopark in Ganzu Province, China.

Liujiaxia Dinosaur National Geopark in Ganzu Province.

The tracks are located in fine sandstone/siltstone in the Early Cretaceous Yanguoxia Formation, on the southeastern edge of the Lanzhou-Minhe Basin. The site contains six dinosaur trackways, made by dinosaurs with two walking toes, with feet measuring approximately 14.8 cm in length and 6.4 cm wide and step lengths of 35.7-37.5 cm.

One of the prints. (A) Photograph. (B) Computerized Photogrammetry image with 0.2 mm contour lines. (C) Outline drawing with 10 cm scale bar. From Xing et al. (2012).

Deinonychosaurs are thought to have been capable of considerable speed when chasing prey, but none of the Liujiaxia track-makers appears to have been moving fast when making the tracks. This has no particular significance, since no modern predator runs all, or even most, of the time. There has been an ongoing debate over whether these dinosaurs were pack or solitary hunters; again this site is somewhat ambivalent, as most of the tracks are of solitary animals, but one track apparently shows six animals moving as a group.

Turning trackway. Left, photograph. Centre, outline drawing. Right, pace angulations. Scale bar is 50 cm. From Xing et al. (2012).

It is not possible to say with confidence what the actual track-maker was. The print are within the size range of a large Troodontid or a small-to-medium sized Dromaeosaur, though Xing et al. feel that the most likely track-maker was a Dromaeosaur.