Nemegtomaia is a genus of oviraptorid dinosaur from what is now Mongolia that lived in the Late Cretaceous Period, about 70 million years ago. The first specimen was found in 1996, and became the basis of the new genus and species N. barsboldi in 2004. The original genus name was Nemegtia, but this was changed to Nemegtomaia in 2005, as the former name was preoccupied. The first part of the generic name refers to the Nemegt Basin, where the animal was found, and the second part means "good mother", in reference to the fact that oviraptorids are known to have brooded their eggs. The specific name honours the palaeontologist Rinchen Barsbold. Two more specimens were found in 2007, one of which was found on top of a nest with eggs, but the dinosaur had received its genus name before it was found associated with eggs.

Nemegtomaia is estimated to have been around 2 m (7 ft) in length, and to have weighed 40 kg (85 lb). As an oviraptorosaur, it would have been feathered. It had a deep, narrow, and short skull, with an arched crest. It was toothless, had a short snout with a parrot-like beak, and a pair of tooth-like projections on its palate. It had three fingers; the first was largest and bore a strong claw. Nemegtomaia is classified as a member of the oviraptorid subfamily Ingeniinae, and it the only known member of this group with a cranial crest. Though Nemegtomaia has been used to suggest that oviraptorosaurs were flightless birds, the clade is generally considered a group of non-avian dinosaurs.

The nesting Nemegtomaia specimen was placed on top of what was probably a ring of eggs, with its arms folded across them. None of the eggs are complete, but they are estimated to have been 5 to 6 cm (2 to 2.3 in) wide and 14 to 16 cm (5 to 6 in) long when intact. The specimen was found in a stratigraphic area that indicates Nemegtomaia preferred nesting near streams that would provide soft, sandy substrate and food. Nemegtomaia may have protected its eggs by covering them with its tail and wing feathers. The skeleton of the nesting specimen has damage that indicates it was scavenged by skin beetles. The diet of oviraptorids is uncertain, but their skulls are most similar to other animals that are known or thought to have been herbivorous. Nemegtomaia is known from the Nemegt and Baruungoyot Formations, which are thought to represent humid and arid environments that coexisted in the same area,

Temporal range: Late Cretaceous, 70 Ma
Nemegtomaia barsboldi holotype
Skeletal diagram showing known remains of the holotype specimen, MPC-D 100/2112
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Order: Saurischia
Suborder: Theropoda
Family: Oviraptoridae
Subfamily: Ingeniinae
Genus: Nemegtomaia
et al., 2005
  • N. barsboldi (Lü et al., 2004)
  • Nemegtia barsboldi Lü et al., 2004


Nemegtomaia size
Size compared to a human

Nemegtomaia is estimated to have been around 2 m (7 ft) in length, and to have weighed 40 kg (85 lb), a size extrapolated from more completely known relatives. As an oviraptorosaur, it would have been feathered. The neural spines of the neck (cervical) vertebrae were short, and the neural arches had an x-shaped appearance. The middle three of these vertebrae were the largest. The scapula (shoulder blade) appears to have been 185 mm (7 in) in total length. The humerus (upper arm bone) had a fossa (depression) in a position similar to modern birds, but atypical among oviraptorosaurs, and appears to have been 152 mm (6 in) long. The radius of the lower arm was straight, oval in cross-section, and may have been 144 mm (5 in) long. The first finger was relatively large and had a strong ungual (claw bone), and was more massive than the two other fingers. The second finger was slightly longer than the first, and the third finger was the smallest. The upper margin of the ilium of the pelvis was straight, and though both ilia were close to each other, they were not fused together. The pubic shaft was turned backwards. The femur (thigh bone) is estimated to have been 286 mm (11 in) long, and the tibia of the lower leg 317 mm long (12 in).[1][2]

Nesting Nemegtomaia
Restoration of a nesting individual

The skull of Nemegtomaia was deep, narrow, and short (compared to the rest of the body), and reached 179 mm (7 in) in length. It had a well-developed crest, formed by the nasal and premaxilla bones (mainly the latter) of the snout. The nearly vertical front margin of the holotype's crest formed an almost 90 degree angle with the upper margin of the skull. Compared to other oviraptorids, the nasal processes (projections) of the premaxillae were barely visible when viewed from above (where they connected with the nasal bones on the highest points of the crest). The crest extended hindwards and down, forming a round arch at the highest point. The diameter of the orbit (eye opening) was 52 mm (2 in); the eyes looked large due to the shortness of the skull. The antorbital cavity in front of the eye consisted of two fenestrae (openings); a large antorbital fenestra at the back, and a small maxillary fenestra at the front. Nemegtomaia was distinct from other oviraptorids in that the frontal bone on the midline of the skull was about 25% the length of the parietal bone from front to back. The nares (external nostrils) were relatively small and placed high on the skull.[1][2]

Nemegtomaia MPC-D 107-15 skull
Preserved parts and reconstruction of specimen MPC-D 107/15's skull

The jaws of Nemegtomaia were toothless, and like other oviraptorid dinosaurs, it had a short snout with a deep, robust, and somewhat parrot-like beak. It had a hard palate formed by the premaxillae, vomers, and maxillae, like other oviraptorids. The palate was strongly concave (downwards-projecting), and had a cleft on the central part. As in other oviraptorids, it had a pair of tooth-like projections on the palate that were directed downwards (a feature that has been called "pseudo-teeth"). Nemegtomaia had small foramina (openings) on the sides of the suture (joint) between the premaxillae at the front of the snout, which may have been nutrient openings (and which indicate the presence of a keratinous bill). The lower jaw was short and deep, with a convex lower surface, and reached 153 mm (6 in) in length. The dentary bone of the lower jaw reached 50 mm (2 in) at its highest point. The mandibular symphysis (where the two-halves of the lower jaw connected) was short, deep, and very pneumatised (with air-spaces). The mandibular fenestra was large and was located at the front part of the lower jaw.[1][3][2][4] As in most other oviraptorids, the front of the lower jaw was down-turned.[5]

Though Nemegtomaia does not possess any single feature that distinguishes it from other oviraptorids (autapomorphies), the combination of a crest, an enlarged first finger, and a high number of sacral vertebrae (eight), is unique to this taxon.[6]

History of discovery

Nemegtomaia maps
Maps showing the Nemegt locality (a, b) and where Nemegtomaia specimens have been found (c)

In 1996 the Japanese palaeontologist Yoshitsugu Kobayashi (as part of the "Mongolian Highland International Dinosaur Project" team) found an incomplete skeleton of an oviraptorid dinosaur in the Nemegt Formation of the Gobi Desert in southwestern Mongolia. The specimen (MPC-D 100/2112 at the Mongolian Palaeontological Center, formerly PC and GIN 100/2112), consists of a nearly complete skull and a partial skeleton, including cervical, dorsal, sacral, and caudal vertebrae, a left scapula, the lower ends of both humeri, the right radius, both ilia, the upper ends of both pubic bones, both ischia, and the upper end of a femur. The specimen was described as a new specimen of the genus Ingenia (referred to as Ingenia sp.; of uncertain species) by the Chinese palaeontologist Lü Junchang and colleagues in 2002, and used to highlight the similarities between oviraptorosaurs and birds.[4][1][2]

Skeletal diagrams showing the preserved elements of the three known specimens in grey, composite on right

In 2004 Lü and colleagues determined that the skeleton belonged to a new, distinct taxon, and made it the holotype specimen of Nemegtia barsboldi. The genus name refers to the Nemegt Basin, and the specific name honours the Mongolian palaeontologist Rinchen Barsbold, the leader of the team that found the specimen.[1] In 2005 the describers discovered (after being notified by a biologist) that the name Nemegtia had already been used for a genus of freshwater seed shrimp (Ostracoda) from the same formation in 1978, and was therefore preoccupied. They proposed instead the new genus name Nemegtomaia ("maia" means "good mother" in Greek, and the full name means "good mother of the Nemegt"), making reference to the then-recent discovery that oviraptorids brooded eggs rather than stealing them, though no trace of a nest or eggs had yet been found associated with Nemegtomaia itself.[7][8] The first known member of the oviraptorid family was found with a nest of eggs originally thought to have belonged to the ceratopsian genus Protoceratops, and was therefore named Oviraptor in 1924; this name means "egg-seizer". In the 1990s more oviraptorid specimens were discovered associated with nests and eggs, wherein oviraptorid embryos were found, thereby proving that the eggs belonged to the oviraptorids themselves.[9][10][11] Ingenia was similarly renamed as Ajancingenia in 2013, since the former genus name was preoccupied by a roundworm (Nematoda).[12]

Nemegtomaia nest
Nest diagram (A), bones of the nesting specimen that covered eggs (B–D), and a lower layer of eggs (E–G)

In 2007 two new specimens of Nemegtomaia were found by the "Dinosaurs of the Gobi" expedition, and were described by the Italian palaeontologist Federico Fanti and colleagues in 2013. The first specimen, MPC-D 107/15, was found by Fanti (who nicknamed it "Mary") in the Baruungoyot Formation, and consists of a nest with the presumed parent on top. As the fourth genus of oviraptorid found on top of a nest (after Oviraptor, Citipati, and cf. Machairasaurus), Nemegtomaia had therefore received a genus name referring to this feature before it was itself found associated with eggs. The specimen was excavated from a vertical cliff under "difficult circumstances", including heavy rain and collapsing sandstone blocks. The skeleton preserves parts of the skull, both scapulae, the left arm and hand, the right humerus, the pubic bones, the ischia, the femora, the tibiae, fibulae, and the lower portions of both feet. This specimen was found less than 500 m (1640 ft) from the holotype, and was of the same size; it was assigned to Nemegtomaia due to its similar anatomical features and geographical proximity. It was collected in a single block so that the spatial relationship of the bones and eggs would be preserved. The second specimen, MPC-D 107/16, was found by the American palaeontologist Nicholas R. Longrich in the Nemegt Formation, and consists of the hands, a partial left ulna and radius, ribs, a partial pelvis, and both femora. This specimen was 35% smaller than the others, and was assigned to Nemegtomaia due to its hands having the same characteristics as those of specimen MPC-D 107/15. It is possible that the hands may have belonged to a different individual, as they were not found articulated with the rest of the skeleton (other oviraptorids are known from quarries with multiple skeletons), but this cannot be confirmed.[2][8]


In their 2004 phylogenetic analysis, Lü and colleagues classified Nemegtomaia as a derived (or "advanced") oviraptorosaur, and found it to be most closely related to the genus Citipati.[1] In 2010 Longrich and colleagues determined that Nemegtomaia belonged in the family Oviraptoridae, as part of the subfamily Ingeniinae, making it the only member of the latter group with a prominent crest. Members of the other recognised subfamily, Oviraptorinae, all possess crests. Ingeniines are distinguished by smaller size, short and robust forelimbs with weakly curved claws, the number of vertebrae in the synsacrum, as well as certain features of the feet and pelvis. Longrich and colleagues suggested that the presence of a crest on Nemegtomaia makes it possible that this feature evolved or disappeared several times among oviraptorids, or that the animal may not have been an ingeniine.[13][2]

In 2012 Fanti and colleagues also found Nemegtomaia to be part of Ingeniinae (as a derived member, closest to Heyuannia), due to the proportions of the hands of the two new specimens (relatively short with a robust first finger). They stated that, though the presence of crests is generally associated with oviraptorines rather than ingeniines, the feature may be correlated with size and maturity. They pointed out that the nasal and frontal bones of the ingeniine Conchoraptor were pneumatic and could potentially have grown into a crest as the animal matured, though all known skeletons of that genus are of the same small size (and one specimen appears to have been fully grown). The cladogram below shows the placement of Nemegtomaia within Oviraptoridae, according to Fanti et al., 2012:[2]

Restorations of oviraptorid heads shown to scale; K is Nemegtomaia












"Ingenia" (=Ajancingenia)





Oviraptorosaur manus
Hand bones of oviraptorosaurs compared; P is the hand of Nemegtomaia, grouped within Ingeniinae

The clade Oviraptorosauria is generally regarded as a group of non-avian (or non-bird) theropod dinosaurs, and their similarity to birds (Aves) has often been noted. Fossils of oviraptorosaurs in the family Caenagnathidae have historically been confused with those of birds, and some researchers have gone so far as to consider oviraptorosaurs as a whole more closely related to birds than to other non-avian dinosaurs. In 2002 Lü and colleagues used the then unnamed Nemegtomaia to show similarities between birds and oviraptorosaurs, and found the latter group to be closer to birds than to bird-like dinosaurs such as dromaeosaurs. They therefore concluded that oviraptorosaurs were flightless birds rather than non-avian dinosaurs, and noted that the boundary between birds and dinosaurs was becoming more and more difficult to delineate.[4] Other researchers have instead found dromaeosaurs and troodontids to be most closely related to birds, together forming the group Paraves; oviraptorosaurs, therizinosaurs, and alvarezsaurs are just outside this group. The wider group that includes oviraptorosaurs and Paraves is called Pennaraptora, and this group is defined by the presence of pennaceous feathers (feathers with a stalk).[14]

Oviraptorosaurs are known from Asia (where they may have originated) and North America, and are mainly known from deposits that date from the Campanian-Maastrichtian ages of the Cretaceous period. The group includes small to large members, and they are characterised by their short skulls and beaks, elongated fingers, and short tails. Basal (or "primitive") members had teeth, which disappeared in derived members of the group (those within the superfamily Caenagnathoidea, which includes Oviraptoridae). They were at least partially herbivorous, and brooded their nests in a bird-like posture. Though they are all thought to have to been feathered, they appear to have been flightless. Cranial crests appear to have evolved convergently in different lineages within the group.[14] The family Oviraptoridae (to which Nemegtomaia belongs) consisted of generally small members, and is exclusively known from the Upper Cretaceous of Asia, with most genera having been discovered in the Gobi Desert of Mongolia and China.[13] Including Nemegtomaia, at least nine oviraptorid genera have been discovered in a relatively small geographical area in the Gobi Desert.[15][6]



Nemegtomaia nesting
Diagram showing the remains and body outline of the nesting specimen

The Nemegtomaia specimen MPC-D 107/15 was found associated with a nest with eggs; its feet were placed in the centre of what was probably a ring of eggs, with the arms folded across the tops of the eggs on each side of the body, a posture similar to what is seen in other fossils of brooding oviraptorids. The collected part of the nest is about 90 cm (35 in) wide and 100 cm (30 in) long; the skeleton occupies the upper 25 cm (10 in) of the block, whereas the remaining 20 cm (8 in) is occupied by broken eggs and shells. There is no evidence of plant material in the nest, but there are fragments of undetermined bones. The nest does not preserve any complete eggs or embryos, which prevents determination of the size, shape, number, and arrangement of the eggs in the nest. It is probable that there were originally two layers of eggs below the body, and there do not appear to have been eggs in the centre of the nest. Most eggs (seven distinct eggs have been identified) and egg fragments were recovered either in the lower layer of the nest or under the skull, neck, and limbs of the specimen, and the bones either rested directly on the eggs or were within 5 mm (0.2 in) of their surfaces. That the skeleton was directly positioned on top of it shows that the nest was not completely covered by sand. Though the placement of the eggs does not suggest a specific arrangement in the nest, most other oviraptorid nests show that the eggs were arranged in pairs in up to three levels of concentric circles. The eggs of MPC-D 107/15 were therefore most likely displaced during burial, or by external factors, such as strong winds, sandstorms, or predators. This also supports the idea that the upper layer of eggs was not buried, as fully buried eggs would have been less likely to be transported by external factors.[2]

Nemegtomaia eggs
Details of eggs preserved with the nesting specimen

Oviraptorid eggs appear to have been 17 cm (6 in) long on average, and the most complete eggs found with MPC-D 107/15 are thought to have been 5 to 6 cm (2 to 2.3 in) wide and 14 to 16 cm (5 to 6 in) long when intact. The eggs are nearly identical to some that have previously been found in Mongolia, and have therefore been assigned to the oofamily (egg-taxon family) Elongatoolithidae. The eggshells are relatively thin, between 1 and 1.2 mm (0.03 and 0.04 in), and their outer surface is covered by ridges and nodes that rise about 0.3 mm (0.01 in) above the shell. The micro-structure of the eggshells could not be properly studied, as the calcite has been heavily altered and re-crystallized.[2]

The nesting specimen was found in a stratigraphic area indicating that oviraptorids preferred nesting near streams that provided soft, sandy substrate and food in environments that were otherwise xeric (receiving a small amount of moisture). Many oviraptorids have been found in brooding positions, indicating they may have brooded for relatively long periods, similar to modern birds such as the ostrich, emu, and black-breasted buzzard, which brood for more than 40 days with a limited supply of sustenance. Nesting in desert environments can be harmful to adults that stay in the nest for large parts of the day, and for eggs and nestlings, due to heat stress. The choice of nesting area may therefore have been a mechanism for successful incubation in extreme heat. It has also been suggested that the evolution of tail-feathers in oviraptorosaurs was an adaptation for shading and protecting eggs in their nests. That the second finger of ingeniine oviraptorids was reduced in size compared to the robust first finger may be explained by a change in function; it may be related to the presence of long wing feathers that were attached to the second finger. These wing feathers were probably used to protect the eggs during nesting. When the second finger began functioning as a feather support, its ability to grasp was reduced, and this function was taken over by the first finger, which therefore became more robust. The third finger was reduced in size, too, probably because it was positioned behind the wing feathers in a way where it would not be effective for grasping.[2]

Autruche male
The brooding behaviour of oviraptorids is thought to have been similar to that of palaeognath birds; here, a male Somali ostrich

Various studies have suggested that several individuals would gather eggs in a single nest, and arrange them so they could be protected by one individual, possibly a male.[2] In 2010 the American palaeontologist David J. Varricchio and colleagues found that the relatively large clutch-size of oviraptorids and troodontids is most similar to those of modern archosaurs (birds and crocodilians, the closest living relatives of dinosaurs) that practice polygamous mating and extensive male parental care (as seen in paleognaths such as ostriches and emus). This reproductive system pre-dates the origin of birds and would therefore be the ancestral condition for modern birds, with biparental care (where both parents participate) being a later development.[16] Many oviraptorosaurs are known to have had pygostyles on the end of their tails, which suggests the presence of feather-fans; these could have been used for intraspecific communication such as courtship rituals.[17]

Diet and feeding

Nemegtomaia jaw
Lower jaw of the holotype specimen, with beak on the right

The diet of oviraptorids has been interpreted in various ways since the time Oviraptor was wrongly thought to have been a predator of eggs. It has been suggested that oviraptorosaurs as a whole were herbivores, which is supported by the gastroliths (stomach stones) found in Caudipteryx, and the wear facets in the teeth of Incisivosaurus. In 2010 Longrich and colleagues found that oviraptorid jaws had features similar to those seen in herbivorous tetrapods (four-limbed animals), especially those of dicynodonts, an extinct group of synapsid stem-mammals. Oviraptorids and dicynodonts share features such as short, deep, and toothless mandibles; elongated dentary symphyses; elongated mandibular fenestrae; and a downwards-projecting bar in the palate. Modern animals with jaws that resemble those of oviraptorids include parrots and tortoises; the latter group also has tooth-like projections on their premaxillae. Longrich and colleagues concluded that due to the similarities between oviraptorids and herbivorous animals, the bulk of their diet would most likely have been formed by plant matter. Oviraptorids are found at high frequencies in the formations they are known from, similar to the pattern seen in dinosaurs that are known to be herbivorous; these animals were more abundant than carnivorous dinosaurs, as more energy was available at their lower trophic level in the food chain. The jaws of oviraptorids may have been specialised for processing food, such as xerophytic vegetation (adapted for environments with little water), that would have grown in their environment, but this is not possible to demonstrate, as little is known about the flora of the area at the time.[13] A 2013 study by Lü and colleagues found that oviraptorids appear to have retained their hind limb proportions throughout ontogeny (growth), which is also a pattern mainly seen in herbivorous animals.[18] In 2017, the Canadian palaeontologist Gregory F. Funston and colleagues suggested that the parrot-like jaws of oviraptorids may indicate a frugivorous diet that incorporated nuts and seeds.[6]

Nemegtomaia hands
Diagrams showing the hands of specimen MPC-D 107/15 and 107/16

In 1977 Barsbold suggested that oviraptorids fed on molluscs, but Longrich and colleagues rejected the idea that they practised shell-crushing altogether, since such animals tend to have teeth with broad crushing surfaces. Instead, the shape of the dentary bones in the lower jaws of oviraptorids suggests they had a sharp-edged beak used for shearing tough food, not for cracking hard food items such as bivalves or eggs. The symphyseal shelf at the front of the dentary may have given some ability for crushing, but as this was a relatively small area, it was probably not the main function of the jaws. The fact that most oviraptorids have been found in sediments that are interpreted as having been xeric and arid or semi-arid environments also argues against them having been specialised eaters of shellfish and eggs, as it is unlikely there would have been enough of these items under such conditions to support them.[13]

Longrich and colleagues pointed out that the robust forelimbs and enlargement of a single finger in ingeniine oviraptorids is similar to that seen in modern animals that eat ants and termites, such as anteaters and pangolins, but the morpholology of ingeniine jaws does not support them being insectivorous. The researchers found that the function of ingeniine forelimbs was unclear, but suggested that they could have been used for scratching, tearing, or digging, though not prey capture.[13]

In 2004 Lü and colleagues proposed that the articulation between the quadrate and quadratojugal bones in the skull of Nemegtomaia suggested that these bones were movable in relation to each other, which would have affected how the jaws functioned. In 2015 the Belgian palaeontologist Christophe Hendrickx and colleagues found it unlikely that Nemegtomaia and other oviraptords had bird-like kinesis in their skulls, due to the quadrate bone being immobile.[19]


Nemegtomaia stratigraphy
Map and diagram showing the relation between the interfingering Baruungoyot and Nemegt Formations

Nemegtomaia is known from the Nemegt and Baruungoyot Formations, which date to the upper Campanian–lower Maastrichtian ages of the Late Cretaceous period, about 70 million years ago. Though this taxon is known only from the Nemegt locality, unidentified oviraptorid remains from other localities may belong to it. The Nemegt massif has numerous canyons or gorges, up to 45 metres (148 ft) deep, which have some of the best exposures of these formations. The rock facies of the Nemegt Formation are thought to represent a humid, fluvial (associated with rivers and streams) environment, whereas those of the Baruungoyot Formation are thought to represent an arid or semi-arid environment, with aeolian (affected by wind) beds. These two formations with their diverse fossils were historically thought to represent sequential time periods with different environments, but in 2009 the Canadian palaeontologist David A. Eberth and colleagues found that there was partial overlap across the transition between them. The two formations "interfinger" across a stratigraphic interval that is about 25 m (82 ft) thick, which suggests that the fluvial and aeolian environments coexisted when the area was sedimented.[2][20][21][6]

Nemegt and Baruungoyot Formations
Photos of the interfingering contacts between the formations

The environment of the Nemegt Formation has been compared to the Okavango Delta of present-day Botswana.[22] The habitats in and around the Nemegt rivers provided a home for a wide array of organisms. Aquatic animals include molluscs, fish, turtles, and the crocodylomorph Shamosuchus. Fossils of mammals such as multituberculates have been found, and birds such as Gurilynia, Judinornis, and Teviornis are known. Herbivorous dinosaurs of the Nemegt Formation include ankylosaurids such as Tarchia, the pachycephalosaurian Prenocephale, hadrosaurids such as Saurolophus and Barsboldia, and sauropods such as Nemegtosaurus, and Opisthocoelicaudia. Other theropods include tyrannosauroids such as Tarbosaurus, Alioramus, and Bagaraatan, troodontids such as Borogovia, Tochisaurus, and Saurornithoides, therizinosaurs such as Therizinosaurus, and ornithomimosaurians such as Deinocheirus, Anserimimus, and Gallimimus.[23][24][25]

Other oviraptorosaur genera known from the Nemegt Formation include the basal Avimimus, the oviraptorids Rinchenia, Nomingia, and Ajancingenia, and the caenagnathid Elmisaurus. In addition, Conchoraptor is known from the Baruungoyot Formation. In spite of the high number of oviraptorid taxa in these formations (the Nemegt has the highest known diversity of them anywhere), none of them were closely related. The Nemegt Formation is unique in having both oviraptorid and caenagnathid oviraptorosaurs, and in 1993 the Canadian palaeontologist Phillip J. Currie and colleagues suggested this diversity was due to the two groups preferring different environments in the area. In 2016 the Japanese palaeontologist Takanobu Tsuihiji and colleagues suggested that oviraptorids may have preferred drier environments, while caenagnathids preferred fluvial environments, based on the type of formations they have been found in.[26][2] Funston and colleagues suggested that oviraptorids were found in both xeric and mesic environments (but were more abundant in the former), whereas the other oviraptorosaur groups avoided the xeric environments, and that the coexistence of the families can be explained by niche partitioning in diet. The environment of the Nemegt Formation may have acted as an oasis and thereby attracted oviraptorids.[6]


Beetle feeding traces in Nemegtomaia
Feeding traces from skin beetles on the nesting specimen

The nesting specimen MPC-D 107/15 has provided much information about the taphonomic processes (changes during decay and fossilisation) in the Baruungoyot Formation. The specimen is preserved in facies that are thought to have been deposited through a sandstorm or dune-shift. It does not seem to have been transported after death, but the body appears to have shifted slightly to the right, indicating the sediment in which it was deposited came towards it from its left side. The neck is curved to the left, the left hand is folded backwards, and the legs are folded into a crouching position. The vertebral column, neck, and hips deteriorated during burial, and much of the damage to the skeleton is thought to have been caused by the activity of invertebrates.[2]

Borings in the bones, burrows, and reworked sediments (perhaps caused by the construction of pupal chambers) in the specimen indicate it was scavenged upon by colonies of skin beetles (Dermestidae) and perhaps other scavenging insects. There are many feeding traces in the joints of the skeleton, and almost all the surfaces where the bones articulated have been obliterated. There are also tunnels in the nest under the neck and skull, and no egg remains have been found in parts with such traces. Modern skin beetles mainly feed on muscle tissue but not on moist materials, and their activity is prevented by rapid burial. It is therefore thought that specimen MPC-D 107/15 was only partially buried at first, with the upper part being exposed enough for a colony of skin beetles to develop. Some damage to the skeleton (especially in the vertebral column) may also have been caused by the scavenging of small mammals.[2]

See also


  1. ^ a b c d e f Lü, J.; Tomida, Y.; Azuma, Y.; Dong, Z.; Lee, Y.-N. (2004). "New oviraptorid dinosaur (Dinosauria: Oviraptorosauria) from the Nemegt Formation of southwestern Mongolia" (PDF). Bulletin of the National Science Museum, Tokyo, Series C. 30: 95–130.
  2. ^ a b c d e f g h i j k l m n o Fanti, F.; Currie, P. J.; Badamgarav, D.; Lalueza-Fox, C. (2012). "New specimens of Nemegtomaia from the Baruungoyot and Nemegt Formations (Late Cretaceous) of Mongolia". PLoS ONE. 7 (2): e31330. Bibcode:2012PLoSO...731330F. doi:10.1371/journal.pone.0031330. PMC 3275628. PMID 22347465.
  3. ^ Paul, G.S. (2010). The Princeton Field Guide to Dinosaurs. Princeton University Press. pp. 152, 154. ISBN 978-0-691-13720-9.
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Caudipteryx (which means "tail feather") is a genus of peacock-sized theropod dinosaurs that lived in the Aptian age of the early Cretaceous Period (about 124.6 million years ago). They were feathered and remarkably birdlike in their overall appearance.

Two species have been described; C. zoui (the type species), in 1998, and C. dongi, in 2000.Caudipteryx fossils were first discovered in the Yixian Formation of the Sihetun area of Liaoning Province, northeastern China in 1997.


Citipati (pronounced [ˈtʃiːt̪ɪpət̪i] in Hindi, meaning 'funeral pyre lord') is a genus of oviraptorid theropod dinosaur from the Late Cretaceous Period of what is now Mongolia (specifically, the Djadokhta Formation of Ukhaa Tolgod, in the Gobi Desert). It is one of the best-known oviraptorids, thanks to a number of well-preserved skeletons, including several specimens found in brooding positions atop nests of eggs. These nesting specimens have helped to solidify the link between non-avian dinosaurs and birds.

The type species, Citipati osmolskae, was described in 2001. A second, as yet unnamed species may also exist. Citipati is often confused with the similar Oviraptor.


Conchoraptor (meaning "conch plunderer") is a genus of oviraptorid dinosaur from the late Cretaceous Period of what is now Asia.


Corythoraptor (meaning "crested raptor") is a genus of crested oviraptorid theropod dinosaur from the Nanxiong Formation of China. It is known from one species, C. jacobsi, named after palaeontologist Louis L. Jacobs. Including it, there are seven oviraptorids known from the Nanxiong Formation, showing a high level of diversity in the area, and that the different taxa may have occupied different ecological niches.


Elongatoolithidae is an oofamily of fossil eggs, representing the eggs of oviraptorosaurs (with the exception of the avian Ornitholithus). They are known for their highly elongated shape. Elongatoolithids have been found in Europe, Asia, and both North and South America.


Heyuannia ("from Heyuan") is a genus of oviraptorid dinosaur that lived during the Late Cretaceous Period in China. It was the first oviraptorid found in that country; most others were found in neighbouring Mongolia. Two species are known: H. huangi, named by Lü Junchang in 2002; and H. yanshini, originally named as a separate genus Ingenia by Rinchen Barsbold in 1981 (and renamed to Ajancingenia in 2013 due to the preoccupation of Ingenia).


Huanansaurus is an extinct genus of oviraptorid dinosaur that lived approximately 72 million years ago, between the Campanian and Maastrichtian, during the latter part of the Cretaceous period in what is now China, in the Nanxiong Formation.


Khaan (; Mongol [χaːŋ] 'lord') was an oviraptorid dinosaur that was found in the Djadochta Formation of Mongolia and lived in the Late Cretaceous Period (Campanian), 75 million years ago.

List of Asian dinosaurs

This is a list of dinosaurs whose remains have been recovered from Asia excluding the Indian Subcontinent, which was part of a separate landmass for much of the Mesozoic. This list does not include dinosaurs that live or lived after the Mesozoic age such as birds.

List of dinosaur genera

This list of dinosaurs is a comprehensive listing of all genera that have ever been included in the superorder Dinosauria, excluding class Aves (birds, both living and those known only from fossils) and purely vernacular terms.

The list includes all commonly accepted genera, but also genera that are now considered invalid, doubtful (nomen dubium), or were not formally published (nomen nudum), as well as junior synonyms of more established names, and genera that are no longer considered dinosaurs. Many listed names have been reclassified as everything from birds to crocodilians to petrified wood. The list contains 1559 names, of which approximately 1192 are considered either valid dinosaur genera or nomina dubia.


Machairasaurus is a genus of oviraptorid dinosaur which was found in the Bayan Mandahu Formation, China dating to the late Cretaceous period.During the Sino-Canadian expeditions of 1988 and 1990 some skeletons of unknown oviraptorosaurians were discovered by Philip J. Currie in Inner Mongolia. Based on two of these a new genus was named and described by Nicholas R. Longrich, Currie and Dong Zhiming in 2010 with as type species Machairasaurus leptonychus. The generic name is derived from Greek μάχαιρα (makhaira), "short scimitar". The specific name is derived from Greek λεπτός (leptos), "slender", and ὄνυξ (onyx), "claw". The species name as a whole refers to the sabre-like claws of the hand.The holotype, IVPP V15979, was found in layers of the Bayan Mandahu dating from the late Campanian. It mainly consists of a left frontlimb, including the lower end of the lower arm, two carpal bones and a complete hand. Also some fragmentary foot elements were present. The other find is the paratype, IVPP V15980, consisting of a very fragmentary skeleton including tail vertebrae, chevrons, ribs, phalanges of the hands, fragments of the second and fourth metatarsals and pedal phalanges.Five oviraptorid specimens associated with a nest, the female having been found brooding near the eggs, may belong to Machairasaurus.Machairasaurus was a small bipedal theropod. The describers established a single autapomorphy, unique derived trait: the hand claws are very elongated and blade-like in side view, with a length four times that of the joint height. The long claws would be proof that basal oviraptorids used their hands to pull down branches; the more curved claws of more derived forms would have served to dig up roots.Machairasaurus was in 2010 assigned to the Oviraptoridae, more precisely to the Ingeniinae. It formed a smaller clade with "Ingenia" yanshini, Heyuannia huangi, Conchoraptor gracilis, and Nemegtomaia barsboldi.


Nankangia is an extinct genus of caenagnathoid oviraptorosaurian dinosaur known from the Late Cretaceous Nanxiong Formation of Nankang County, Ganzhou City of Jiangxi Province, southeastern China. It contains a single species, Nankangia jiangxiensis. N. jiangxiensis coexisted with at least four other caenagnathoids, including an unnamed oviraptorid, Banji long, Ganzhousaurus nankangensis and Jiangxisaurus ganzhouensis. The relatively short dentary and non-downturned mandibular symphysis of Nankangia suggest that it may have been more herbivorous than carnivorous.

Nemegt Formation

The Nemegt Formation (or Nemegtskaya Svita) is a geological formation in the Gobi Desert of Mongolia, dating to the Late Cretaceous. It overlies and sometimes interfingers with the Barun Goyot Formation. Interfingering has been noted at the stratotype (Red Walls) and Khermeen Tsav. It consists of river channel sediments and contains fossils of fish, turtles, crocodilians, and a diverse fauna of dinosaurs, including birds. The climate associated with it was wetter than when preceding formations were deposited; there seems to have existed at least some degree of forest cover. Fossilized trunks have been also found.

There has been no absolute dating of the Nemegt Formation. It is, however, almost certainly early Maastrichtian c 71-70 Ma. Gradzinski and others considered a Campanian age possible but more recent research indicates otherwise. A Campanian age no longer seems credible, because the Alagteegian (or lower Djadokhtan, at the locality "Chuluut Uul") has been radiometrically dated at about 73.5 Ma or even younger (a more recent K/Ar date is 71.6 +/- 1.6 Ma). The c 73.5 (or perhaps 72) Ma Alagteegian is separated from the Nemegt by the "classic" Djadokhtan (e.g. Bayan Dzag), later Djadohktan (represented by Ukhaa Tolgod) and Barungoyotian (Khulsan). All these intervening horizons almost certainly represent more than the 1.5 million years between the dated Alagteegian level and the onset of Maastrichtian time (72.1 million Ma according to current dating). Ergo the Nemegt is entirely Maastrichtian. See also Shuvalov, Sochava and Martinsson The Age of Dinosaurs in Russia and Mongolia. The presence of Saurolophus further supports an early Maastrichtian age as the same genus occurs in the early Maastrichtian Horseshoe Canyon formation.


Oviraptor is a genus of small Mongolian theropod dinosaurs, first discovered by technician George Olsen in an expedition led by Roy Chapman Andrews, and first described by Henry Fairfield Osborn, in 1924. Its name is Latin for 'egg taker' or "egg seizer", referring to the fact that the first fossil specimen was discovered atop a pile of what were thought to be Protoceratops eggs, and the specific name philoceratops means "lover of ceratopsians", also given as a result of this find. In his 1924 paper, Osborn explained that the name was given due to the close proximity of the skull of Oviraptor to the nest (it was separated from the eggs by only 4 inches or 10 centimetres of sand). However, Osborn also suggested that the name Oviraptor "may entirely mislead us as to its feeding habits and belie its character". In the 1990s, the discovery of nesting oviraptorids like Citipati proved that Osborn was correct in his caution regarding the name. These finds showed that the eggs in question probably belonged to Oviraptor itself, and that the specimen was actually brooding its eggs, when it died at the nest.

Oviraptor lived in the late Cretaceous period, during the late Campanian stage about 75 million years ago; only one definitive specimen is known (with associated eggs), from the Djadokhta Formation of Mongolia, though a possible second specimen (also with eggs) comes from the northeast region of Inner Mongolia, China, in an area called Bayan Mandahu.


Oviraptoridae is a group of bird-like, herbivorous and omnivorous maniraptoran dinosaurs. Oviraptorids are characterized by their toothless, parrot-like beaks and, in some cases, elaborate crests. They were generally small, measuring between one and two metres long in most cases, though some possible oviraptorids were enormous. Oviraptorids are currently known only from the Late Cretaceous of Asia, with the most well-known species and complete specimens found only in the Gobi Desert of Mongolia and northwestern China.


Oviraptorosaurs ("egg thief lizards") are a group of feathered maniraptoran dinosaurs from the Cretaceous Period of what are now Asia and North America. They are distinct for their characteristically short, beaked, parrot-like skulls, with or without bony crests atop the head. They ranged in size from Caudipteryx, which was the size of a turkey, to the 8 metre long, 1.4 ton Gigantoraptor. The group (along with all maniraptoran dinosaurs) is close to the ancestry of birds. Analyses like those of Maryanska et al (2002) and Osmólska et al. (2004) suggest that they may represent primitive flightless birds. The most complete oviraptorosaur specimens have been found in Asia. The North American oviraptorosaur record is sparse.The earliest and most basal ("primitive") known oviraptorosaurs are Ningyuansaurus wangi, Protarchaeopteryx robusta and Incisivosaurus gauthieri, both from the lower Yixian Formation of China, dating to about 125 million years ago during the Aptian age of the early Cretaceous period. A tiny neck vertebra reported from the Wadhurst Clay Formation of England shares some features in common with oviraptorosaurs, and may represent an earlier occurrence of this group (at about 140 million years ago).

Timeline of oviraptorosaur research

This timeline of oviraptorosaur research is a chronological listing of events in the history of paleontology focused on the oviraptorosaurs, a group of beaked, bird-like theropod dinosaurs. The early history of oviraptorosaur paleontology is characterized by taxonomic confusion due to the unusual characteristics of these dinosaurs. When initially described in 1924 Oviraptor itself was thought to be a member of the Ornithomimidae, popularly known as the "ostrich" dinosaurs, because both taxa share toothless beaks. Early caenagnathid oviraptorosaur discoveries like Caenagnathus itself were also incorrectly classified at the time, having been misidentified as birds.The hypothesis that caenagnathids were birds was questioned as early as 1956 by Romer, but not corrected until Osmolska formally reclassified them as dinosaurs in 1976. Meanwhile, the classification of Oviraptor as an ornithomimid persisted unquestioned by researchers like Romer and Steel until the early 1970s when Dale Russell argued against the idea in 1972. In 1976 when Osmolska recognized Oviraptor's relationship with the Caenagnathids, she also recognized that it was not an ornithomimid and reclassified it as a member of the former family. However, that same year Rinchen Barsbold argued that Oviraptor belonged to a distinct family he named the Oviraptoridae and he also formally named the Oviraptorosauria later in the same year.Like their classification, the paleobiology of oviraptorosaurs has been subject to controversy and reinterpretation. The first scientifically documented Oviraptor skeleton was found lying on a nest of eggs. Because its powerful parrot-like beak appeared well-adapted to crushing hard food items and the eggs were thought to belonged to the neoceratopsian Protoceratops, oviraptorosaurs were thought to be nest-raiders that preyed on the eggs of other dinosaurs. In the 1980s, Barsbold proposed that oviraptorosaurs used their beaks to crack mollusk shells as well. In 1993, Currie and colleagues hypothesized that small vertebrate prey may have also been part of the oviraptorosaur diet. Not long after, fossil embryonic remains cast doubt on the popular reconstruction of oviraptorosaurs as egg thieves when it was discovered that the "Protoceratops" eggs that Oviraptor was thought to be "stealing" actually belonged to Oviraptor itself. The discovery of additional Oviraptor preserved on top of nests in lifelike brooding posture firmly established that oviraptorosaurs had been "framed" as egg thieves and were actually caring parents incubating their own nests.


Tongtianlong (meaning "Tongtianyan dragon") is a genus of oviraptorid theropod dinosaurs that lived in the late Maastrichtian epoch of the late Cretaceous period. It contains one species, T. limosus.


Wulatelong is an extinct genus of basal oviraptorid dinosaur known from the Late Cretaceous Wulansuhai Formation (Campanian stage) of Bayan Mandahu, Linhe District of Inner Mongolia, northern China. It contains a single species, Wulatelong gobiensis.

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