A non-avian dinosaur with a streamlined body exhibits potential adaptations for swimming

Abstract

Streamlining a body is a major adaptation for aquatic animals to move efficiently in the water. Whereas diving birds are well known to have streamlined bodies, such body shapes have not been documented in non-avian dinosaurs. It is primarily because most known non-avian theropods are terrestrial, barring a few exceptions. However, clear evidence of streamlined bodies is absent even in the purported semiaquatic groups. Here we report a new theropod, Natovenator polydontus gen. et sp. nov., from the Upper Cretaceous of Mongolia. The new specimen includes a well-preserved skeleton with several articulated dorsal ribs that are posterolaterally oriented to streamline the body as in diving birds. Additionally, the widely arched proximal rib shafts reflect a dorsoventrally compressed ribcage like aquatic reptiles. Its body shape suggests that Natovenator was a potentially capable swimming predator, and the streamlined body evolved independently in separate lineages of theropod dinosaurs.

Presenting Natovenator polydontus, a non-avian dinosaur from the Upper Cretaceous of Mongolia displaying morphology indicative of swimming behaviour.

Introduction

The Gobi Desert of Mongolia is the source of non-avian theropod dinosaurs that provided important evidence for brooding behaviour¹, the presence of pygostyles², and a long-armed giant omnivore³. A recent study of the dromaeosaurid theropod Halszkaraptor from the Djadochta Formation of this region revealed its semiaquatic ecology, which is unique among non-avian maniraptorans⁴. Its morphological specializations include a snout with a complex neurovascular network, retracted nares, a dental arrangement for capturing evasive prey, an unusually long neck similar to that of known aquatic reptiles, and horizontal zygapophyses in the cervical and caudal vertebrae⁴. Moreover, the flattened forelimb bones and the proportions of the manual digits of Halszkaraptor were similar to birds that use their forelimbs for swimming⁴. However, even though several aquatic adaptations were identified in Halszkaraptor, its body shape could not be inferred from the preserved specimen. Hulsanpes⁵ and Mahakala⁶, the closest relatives of Halszkaraptor, are too poorly preserved or are missing key regions to provide clues about the ecology of this clade.

A new theropod dinosaur, Natovenator polydontus gen. et sp. nov., is described based on a well-articulated specimen (Figs. 1, 2, 3a–h, 4a, Supplementary Note 1, and Supplementary Figs. 1–4) from the Baruungoyot Formation at Hermiin Tsav in the southern Mongolian Gobi Desert. This new taxon exhibits anatomical characteristics very similar to the aquatic adaptations in Halszkaraptor^4,7. More importantly, the configuration of its articulated dorsal ribs indicates that it had a dorsoventrally flattened and streamlined body. Because streamlining of the body provides hydrodynamic advantages during swimming^8–12, this particular dorsal rib morphology strongly indicates that Natovenator was a capable swimmer, providing the first compelling evidence of a streamlined body in a non-avian theropod dinosaur. It thus exemplifies the presence of diverse body forms among non-avian theropods. In addition, Natovenator helps us understand the body plans of halszkaraptorines because it shares many specialized features with Halszkaraptor.

Fig. 1. Natovenator polydontus (MPC-D 102/114, holotype).

Photographs (a, c) and line drawings (b, d) of the main block containing most of the specimen in opposite views. cav caudal vertebra, co coracoid, cv cervical vertebra, d dentary, dc distal carpal, dv dorsal vertebra, fem femur, fu furcula, h humerus, mx maxilla, ph phalanx, pm premaxilla, r radius, ul ulna.

Fig. 2. Skull of Natovenator polydontus (MPC-D 102/114, holotype).

a–d Skull in left lateral (a), right lateral (b), dorsal (c), and ventral (d) views. e µCT-rendered image sliced at the point marked on a, showing a cross-section of the premaxillary and anterior maxillary teeth in dorsal view. f Micro-computed tomography (µCT) rendered image of the occipital region in posterior view. g µCT-rendered image of the pterygoid and quadrate. ?bm possible bite mark, d dentary, f frontal, h humerus, l lacrimal, m5 5th maxillary tooth, mx maxilla, na nasal p parietal, p13 13th premaxillary tooth, pl palatine, pm premaxilla, pop paroccipital process, pt pterygoid, q quadrate, rt replacement tooth, sq squamosal, so supraoccipital.

Fig. 3. Postcranial elements and phylogenetic position of Natovenator polydontus (MPC-D 102/114, holotype).

a Anterior cervical vertebrae in left lateral view. b Axis and third cervical vertebra in dorsal view. c Fourth cervical vertebra in dorsal view. d Posterior cervical vertebrae in right lateral view. e Dorsal series in right lateral view. f Anterior caudal vertebrae in right lateral view. g Left forearm elements in medial view and manus in ventral view. h Right foot in ventral view. i Phylogenetic position of Natovenator in Dromaeosauridae. Numbers at each node indicate Bremer support values. at atlas, c3 third cervical vertebra, c4 fourth cervical vertebra, c7 seventh cervical vertebra, c9 ninth cervical vertebra, ch chevron, d7 seventh dorsal vertebra, fem femur, mc I metacarpal I, mt III metatarsal III, mt IV metatarsal IV, poz postzygapophysis, prz prezygapophysis, r radius, r7 seventh dorsal rib, ul ulna, I-2 pedal phalanx I-2.

Fig. 4. Body plan of Natovenator polydontus (MPC-D 102/114, holotype) and dorsal rib morphology of various diving birds and terrestrial taxa.

a Dorsal series of Natovenator in ventral view. b Reconstruction of dorsal vertebrae and ribs of Natovenator in left lateral view. c Skeletal reconstruction of Natovenator with missing parts in dark grey. d–i Dorsal rib morphology of Natovenator (d), diving birds (e–i), common ostrich (j), and Shri devi, a likely terrestrial dromaeosaurid from the Baruungoyot Formation (k) in ventral view (not to scale). l Reconstruction of the fourth dorsal vertebra with corresponding ribs in anterior view. d2 second dorsal vertebra, r2 second dorsal rib, r3 third dorsal rib, r4 fourth dorsal rib.

Results

Dinosauria Owen, 1842

Theropoda Marsh, 1881

Dromaeosauridae Matthew and Brown, 1922

Halszkaraptorinae Cau et al., 2017

Revised diagnosis

Small dromaeosaurids that possess dorsoventrally flattened premaxillae, premaxillary bodies perforated by many neurovascular foramina, enlarged and closely packed premaxillary teeth that utilized delayed replacement patterns, reduced anterior maxillary teeth, dorsolateral placement of retracted external nares, greatly elongated cervical vertebrae, anterior cervical vertebrae with round lobes formed by the postzygapophyses, horizontal zygapophyses, and pronounced zygapophyseal laminae in the anterior caudal vertebrae, mediolaterally compressed ulnae with sharp posterior margins, second and third metacarpals with similar thicknesses, shelf-like supratrochanteric processes on the ilia, elongated fossae that border posterolateral ridges on the posterodistal surfaces of the femoral shafts, and third metatarsals in which the proximal halves are unconstricted and anteriorly convex.

Natovenator polydontus gen. et sp. nov.

Holotype

MPC-D 102/114 (Institute of Paleontology, Mongolian Academy of Sciences, Ulaanbaatar, Mongolia) is a mostly articulated skeleton with a nearly complete skull (See Supplementary Table 1 for measurements).

Locality and horizon

Baruungoyot Formation (Upper Cretaceous), Hermiin Tsav, Omnogovi Province, Mongolia¹³ (Supplementary Fig. 5).

Etymology

Natovenator, from the Latin nato (swim) and venator (hunter), in reference to the hypothesized swimming behaviour and piscivorous diet of the new taxon; polydontus, from the Greek polys (many) and odous (tooth) in reference to the unusually many teeth.

Diagnosis

A small halszkaraptorine dromaeosaurid with the following autapomorphies: wide groove delimited by a pair of ridges on the anterodorsal surface of the premaxilla, premaxilla with an elongated internarial process that overlies nasal and extends posterior to the external naris, 13 premaxillary teeth with large and incisiviform crowns, first three anteriormost maxillary teeth are greatly reduced and are clustered together with the following tooth without any separations by interdental septa, anteroposteriorly long external naris (about 30% of the preorbital skull length), paroccipital process with a anteroposteriorly broad dorsal surface, elongate maxillary process of the palatine that extends anteriorly beyond the middle of the antorbital fenestra, pterygoid with a deep fossa on the medial surface of the quadrate ramus, distinct posterolaterally oriented projection on the lateral surface of atlas, absence of pleurocoels in cervical vertebrae (not confirmed in the missing fifth cervical centrum), posterolaterally oriented and nearly horizontal proximal shafts in the dorsal ribs, hourglass-shaped metacarpal II with distinctly concave medial and lateral surfaces.

Description

The skull of Natovenator is nearly complete, although the preorbital region has been affected by compression and is slightly offset from the rest of the skull (Figs. 1c, d, 2a–d and Supplementary Figs. 1, 2). Near the tip of the snout, the premaxilla is marked by a broad groove. The body of the premaxilla is also dorsoventrally low and is perforated by numerous foramina that lead into a complex network of neurovascular chambers (Supplementary Fig. 1b) as in Halszkaraptor⁴. Similarly, the external naris is positioned posteriorly and is level with the premaxilla-maxilla contact (Fig. 2a, b), although it is marginally behind this position in Halszkaraptor⁴. It is also dorsally placed compared to those of other non-avian theropods and faces dorsolaterally. The exceptionally long external naris and accordingly elongated internarial process of Natovenator (Fig. 2c) are unique among dromaeosaurids but comparable to those in aquatic toothed birds¹⁴ as well as in therizinosaurs^15,16. The frontal is similar to those of other halszkaraptorines^4,17 in that it is vaulted to accommodate a large orbit and has little contribution to the supratemporal fossa. A sharp nuchal crest is formed by the parietal and the squamosal (Supplementary Fig. 2a–e). The latter also produces a shelf that extends over the quadrate head as in other dromaeosaurids¹⁸. The paroccipital process curves gently on the occiput and has a broad dorsal surface that tapers laterally (Fig. 2f and Supplementary Fig. 2b, e). Its ventrolateral orientation is reminiscent of Mahakala¹⁷ but is different from the more horizontal paroccipital process of Halszkaraptor⁴. The occipital condyle is long and constricted at its base. A shallow dorsal tympanic recess on the lateral wall of the braincase is different from the deep one of Mahakala¹⁷. The palatine is tetraradiate with a greatly elongated maxillary process, which extends anteriorly beyond the level of the mid-antorbital fenestra. The pterygoid is missing its anterior portion (Fig. 2g and Supplementary Fig. 2a–e). A deep fossa on the medial surface of the thin quadrate ramus is not seen in any other dromaeosaurids. The mandibles of Natovenator preserve most of the elements, especially those on the left side (Fig. 1a, b, d and Supplementary Figs. 1a, 2). Each jaw is characterized by a slender dentary with nearly parallel dorsal and ventral margins, a surangular partially fused with the articular, a distinctive surangular shelf, and a fan-shaped retroarticular process that protrudes dorsomedially. The upper dentition of Natovenator is heterodont as the premaxillary teeth are morphologically distinct from the maxillary teeth (Fig. 2a, b, e and Supplementary Fig. 1a, c). There are unusually numerous premaxillary teeth tightly packed without any separation of the alveoli by bony septa. The roots of the teeth are long, and the crowns are tall and incisiviform as in Halszkaraptor⁴. Moreover, the large replacement teeth in the premaxilla suggest that the replacement of the premaxillary teeth was delayed as in Halszkaraptor⁴. However, the number of teeth in each premaxilla is 13 in Natovenator, whereas it is only 11 in Halszkaraptor⁴. In the maxilla, the three most anterior maxillary teeth are markedly shorter than the premaxillary teeth and the more posterior maxillary teeth. This pattern is also observed in Halszkaraptor, although the number of shorter maxillary teeth differs as it has two reduced ones⁷. Both the maxillary and dentary teeth have sharp fang-like crowns that lack serrations. Although posteriormost parts are poorly preserved, there are at least 23 alveoli in each of the maxilla and dentary, which suggests high numbers of teeth in both elements.

The neck of Natovenator, as preserved, is twisted and includes ten elongated cervical vertebrae, although most of the 5th cervical is missing (Figs. 1, 3a–d). This elongation of the cervicals results in a noticeably longer neck than those of most dromaeosaurids and is estimated to be longer than the dorsal series. It is, however, proportionately shorter than that of Halszkaraptor, which has a neck as long as its dorsal and sacral vertebra combined⁴. Another peculiarity in the neck of the Natovenator is a pronounced posterolaterally extending projection on the neurapophysis of the atlas (Fig. 3a and Supplementary Fig. 2b, c, e). The postzygapophyses of each anterior cervical are fused into a single lobe-like process as in Halszkaraptor⁴. Pleurocoels are absent in the cervical vertebrae. In contrast, Halszkaraptor has pleurocoels on its 7th–9th cervicals⁴. A total of 12 dorsal vertebrae are preserved (Figs. 1a, b, 3e, 4a and Supplementary Figs. 3a–d). They all lack pleurocoels, and their parapophyses on the anterior and mid-dorsals are placed high on the anterodorsal end of each centrum. Interestingly, the positions of the parapophyses are similar to those of hesperornithiforms^19–21 rather than other dromaeosaurids such as Deinonychus²² or Velociraptor²³. The preserved dorsal ribs, articulated with the second to seventh dorsals, are flattened and posteriorly oriented (Figs. 1, 3e, 4a–d). The proximal shafts are also nearly horizontal, which is indicative of a dorsoventrally compressed ribcage. Each proximal caudal vertebra has a long centrum and horizontal zygapophyses with expanded laminae (Fig. 3f and Supplementary Fig. 3e–i), all of which are characters shared with other halszkaraptorines^4,17. The forelimb elements are partially exposed (Figs. 1a, b, 2a–d, 3e, g). The nearly complete right humerus is proportionately short and distally flattened like that of Halszkaraptor⁴. The shaft of the ulna is mediolaterally compressed to produce a sharp posterior margin as in Halszkaraptor⁴ and Mahakala¹⁷. Metacarpal III is robust and is only slightly longer than metacarpal II. Similarly, metacarpal III is almost as thick and long as other second metacarpals of other halszkaraptorines^4,17. The femur has a long ridge on its posterior surface, which is another characteristic shared among halszkaraptorines⁴. Typically for a dromaeosaurid, metatarsals II and III have ginglymoid distal articular surfaces (Fig. 3h and Supplementary Fig. 4f, h). The ventral surface of metatarsal III is invaded by a ridge near the distal end, unlike other halszkaraptorines (Fig. 3h)^4,5,17,24.

Phylogenetic analysis

The phylogenetic analysis found more than 99,999 most parsimonious trees (CI = 0.23, RI = 0.55) with 6574 steps. Deinonychosaurian monophyly is not supported by the strict consensus tree (Supplementary Fig. 6). Instead, Dromaeosauridae was recovered as a sister clade to a monophyletic clade formed by Troodontidae and Avialae, which is consistent with the results of Cau et al.⁴ and Cau⁷. Halszkaraptorinae is positioned at the base of Dromaeosauridae as in Cau et al.⁴, although there are claims that dromaeosaurid affinities of halszkaraptorines are not well supported²⁵. Nine (seven ambiguous and two unambiguous) synapomorphies support the inclusion of Halszkaraptorinae in Dromaeosauridae. The two unambiguous synapomorphies are the anterior tympanic recess at the same level as the basipterygoid process and the presence of a ventral flange on the paroccipital process. A total of 20 synapomorphies (including one unambiguous synapomorphy) unite the four halszkaraptorines, including Natovenator (Supplementary Fig. 7). In Halszkaraptorinae, Halszkaraptor is the earliest branching taxon, and the remaining three taxa form an unresolved clade supported by three ambiguous synapomorphies (characters 121/1, 569/0, and 1153/1). Two of these synapomorphies are related to the paroccipital process (characters 121 and 569), which is not preserved in Hulsanpes^5,24. The other is the presence of an expansion on the medial margin of the distal half of metatarsal III, which is not entirely preserved in the Natovenator. When scored as 0 for this character, Natovenator branches off from the unresolved clade. It suggests that the medial expansion of the dorsal surface of metatarsal III could be a derived character among halszkaraptorines.

Discussion

Many anatomical characteristics of Natovenator are interpreted here as valuable indicators of this taxon’s lifestyle. Specifically, a low and mediolaterally expanded premaxilla with enlarged teeth compared to the posterior dentition, a complex network of neurovascular foramina that is extensively developed on the premaxilla, many teeth in both upper and lower dentitions, a delayed replacement pattern of premaxillary teeth, reduced anterior maxillary teeth, retracted and dorsolaterally facing external nares, a greatly elongated neck, and the horizontal zygapophyses in the cervical and proximal caudal vertebrae are among the ecological indicators shared with Halszkaraptor and many reptiles with aquatic adaptations such as plesiosaurians, turtles, and spinosaurids^4,26. Among them, having retracted nares has been debated that this might not be a proper aquatic adaptation²⁷. Another debatable feature is a delayed replacement pattern of premaxillary teeth, which is not directly related to aquatic habits. Although this is shared with sauropterygians, this pattern allows them to keep providing enlarged teeth^28–30. Based on the relatively large premaxillary teeth of Natovenator and Halszkaraptor⁴, the delayed replacement pattern likely served a similar role. There is also a trend among modern birds that aquatic taxa possess long necks, presumably related to feeding habits and bracing impacts during dives³¹. In the case of the Natovenator, the elongated neck might have aided in catching prey rather than in reducing impact because it is unlikely to be able to fly. Additionally, Natovenator provides additional insight into its semiaquatic ecology with its dorsal rib morphology. The dorsal ribs of the Natovenator are directed posterolaterally to a substantial extent (Figs. 3e, 4a–d). Therefore, the angle between each rib shaft and its associated articulating vertebra is very low, like many diving birds, but in contrast to terrestrial theropods (Fig. 4e–k and Table 1). In these diving birds, backward-oriented ribs aid swimming by making the body more streamlined^32,33. This is natural because the posterior orientation of the ribs lowers the dorsoventral height of the body and lengthens the ribcage. The resulting long ribcage then contributes to streamlining the body in diving birds³⁴. In addition to diving birds, the semiaquatic modern platypus³⁵ and possible semiaquatic archosauromorph Tanystropheus³⁶ also possess ribs that extend posteriorly. On the other hand, the ribs in fully aquatic tetrapods such as mosasaurs and extant cetaceans are posteriorly oriented relative to the long axis of the body parts because of inclined thoracic vertebrae, and the anterior migration of the ribcage and abdominal organs is also instrumental in streamlining their bodies^37–41. Consequently, Natovenator acquired a similar rib profile to that of semiaquatic amniotes (Table 2). Another notable feature of the dorsal ribs of the Natovenator is that the proximal shaft forms a wide arch (Fig. 4l), which suggests it had a dorsoventrally compressed ribcage. This barrel-shaped ribcage is also known in putative semiaquatic vertebrates, including spinosaurids^42,43 and choristoderes^44,45. The rib morphology of Natovenator thus implies convergences with various (semi-)aquatic sauropsids and further supports its semiaquatic lifestyle. Also, the streamlined body inferred from the rib configuration strongly indicates that Natovenator was a potentially efficient swimmer (Fig. 5). Although the mode of locomotion in water for the Natovenator is unknown, based on its close phylogenetic relationship with Halszkaraptor (Fig. 3i), forelimbs probably were the primary source of propulsion when swimming, as has been suggested for the latter⁴. Furthermore, the rib morphology of the Natovenator helps resolve the debate on the ecology of Halszkaraptor^5,46. Based on the numerous similarities between Natovenator and Halszkaraptor, it is reasonable to assume that the latter also had a streamlined body and a similar lifestyle. The previous argument that Halszkaraptor represents a transitional taxon rather than a semiaquatic one⁴⁶ thus can be refuted.

Table 1.

Dorsal rib angles of Natovenator polydontus, various diving birds, and terrestrial taxa measured in ventral view.

	Rib angle (°)
Taxon	r2	r3	r4	r5	r6	r7	r8	r9
Natovenator polydontus	48	40	39	34	N/A	38	N/A	N/A
Alle alle	66	70	66	55	47	42	48	43
Alca torda	66	67	62	55	51	47	42	-
Gavia immer	52	64	58	56	54	52	48	48
Anhinga anhinga	55	60	56	62	70	77*	-	-
Aptenodytes patagonicus	62	64	62	68	66	53	48	-
Struthio camelus	131	134	131	130	114	116	117	-
Shri devi	N/A	80	84	N/A	N/A	N/A	89	N/A

Proximal rib shaft angles are measured against the vertebral column. Diving birds include Alle alle, Alca torda, Gavia immer, Anhinga anhinga, and Aptenodytes patagonicus. Terrestrial taxa include Struthio camelus and Shri devi.

r2–r9 indicate second–ninth dorsal (thoracic) ribs.

*This value is the angle of the first sacral rib.

Table 2.

Rib morphology in Natovenator polydontus and other tetrapods with streamlined bodies.

Taxon	Rib orientation	Anterior migration of the ribcage	Lifestyle
Natovenator polydontus	Posterior	Absent	Semiaquatic
Diving birds	Posterior	Absent	Semiaquatic
Ornithorhynchus anatinus	Posterior	Absent	Semiaquatic
Mosasaurs	Slightly posterior	Present	Fully aquatic
Extant cetaceans	Slightly posterior	Present	Fully aquatic

Fig. 5. Life reconstruction of Natovenator polydontus (Artwork by Yusik Choi).

The reconstruction shows the proposed swimming behaviour of Natovenator polydontus.

The morphology of the Natovenator also provides vital information for understanding the body plan of halszkaraptorines because it has many anatomical characteristics previously restricted to Halszkaraptor, including the shared ecological indicators described here. Specifically, the horizontal zygapophyses of the proximal caudal vertebrae are shared with Mahakala¹⁷. It is also notable that Natovenator is from the Baruungoyot Formation, whereas Halszkaraptor is from the Djadochta beds. The striking similarities between Natovenator and Halszkaraptor demonstrate that halszkaraptorines in both Baruungoyot and Djadochta formations probably occupied nearly identical ecological niches. The halszkaraptorine body plan may thus be applied to Hulsanpes, which is only known from a fragmentary skeleton^5,24. The streamlined body of the Natovenator also reflects the high diversity of body shapes among non-avian dinosaurs and exemplifies convergent evolution with diving birds.

Ever since land vertebrates emerged, many different groups have secondarily adapted to aquatic environments⁴⁷. Dinosaurs have been peculiar in this regard because only avian dinosaurs are known for various aquatic forms, including extinct clades²¹. The body plan of the Natovenator makes it clear that some non-avian dinosaurs returned to the water.

Methods

µCT scans

Parts of MPC-D 102/114 were scanned by µCT (or X-ray microscope) to effectively visualize their morphology and internal structures. The skull (excluding its most posterior region) and preserved partial sacrum were scanned via a Skyscan 1276 from Bruker at the Common Research Facility of the School of Biological Sciences at Seoul National University. The back part of the skull with the three anterior cervical vertebrae was scanned by an Xradia 620 Versa from Zeiss at the National Center for Interuniversity Research Facilities at Seoul National University. The parameters used can be found in the Supplementary Information (Supplementary Tables 2, 3). Dragonfly from Object Research Systems was also used in processing the resulting images.

Phylogenetic analysis

To investigate the relationships of Natovenator with other theropods, a phylogenetic analysis was conducted using a revised data matrix from Cau⁷, based on Cau et al.⁴. The modifications that were made in the data matrix are the addition of Natovenator (Supplementary Data 1), removal of four taxa (Alnashetri, Shanag, Fukuivenator, and Hesperornithoides) to prevent collapses of major clades, two character scorings of Mahakala regarding parapophyses of dorsal vertebrae (character 238; from 0 to 1) and the existence of a fibular notch on the calcaneum (character 1430; from ? to 1) based on the description of this taxa from Turner et al.¹⁷. As a result, 182 taxa with 1807 characters (four ordered) were incorporated in our matrix, then analyzed via TNT ver 1.5⁴⁸. The maximum number of trees was set to 99,999, and Herrerasaurus was used as the outgroup taxon. A “New Technology Search” including “Sect. Search” (with RSS, CSS, and XSS checked), “Ratchet,” “Drift,” and “Tree fusing” was performed with default parameters, followed by the final round of “Traditional Search,” also with default parameters, to further explore the shortest trees. Bremer support values at each node were calculated using the Bremer.run script.

Nomenclatural acts

This published work and the nomenclatural acts it contains have been registered in ZooBank, the proposed online registration system for the International Code of Zoological Nomenclature (ICZN). The ZooBank LSIDs (Life Science Identifiers) can be resolved and the associated information viewed through any standard web browser by appending the LSID to the prefix “http://zoobank.org/”. The LSIDs for this publication are: E50586D4-1135-49B8-9912-3B3A4261CEBF for the genus; 9A6C7438-1B6D-4026-AF55-76B604055EA8 for the species.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Author contributions

S.L. processed the µCT data, conducted the phylogenetic analysis, and wrote the manuscript. Y.-N.L. designed and supervised the project. P.J.C. and R.S. discovered and extracted the specimen. R.B. and K.T. provided resources for fieldwork in the Gobi. S.L., J.-Y.P., and S.-H.K. produced the figures. All authors contributed to the discussion and editing of the manuscript.

Peer review

Peer review information

Communications Biology thanks David Hone, Federico Agnolin, and Thomas Holtz Jr. for their contribution to the peer review of this work. Primary Handling Editor: Luke R. Grinham. Peer reviewer reports are available.

Data availability

The character list and scorings (excluding those of Natovetator) are available in Cau⁷. The holotype specimen of Natovenator (MPC-D 102/114) is housed in the Institute of Paleontology in Ulaanbaatar, Mongolia. The µCT scanned images are deposited at morphosource (https://www.morphosource.org/concern/media/000471331 for the skull excluding the occipital region and https://www.morphosource.org/concern/media/000471343 for the occipital region with anterior cervicals).

Code availability

The data matrix of the Natovenator is included in Supplementary Data 1.

Competing interests

The authors declare no competing interests.

Supplementary information

The online version contains supplementary material available at 10.1038/s42003-022-04119-9.