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EXHIBIT 185

Chilantaisaurus

Chilantaisaurus tashuikouensis

Chilantaisaurus is known from large limb bones in Inner Mongolia. Its head and much of its body remain reconstructed. [1]

Evidence profile
PERIODLate Cretaceous[3]
DIETCarnivore (inferred)Evidence and uncertainty in the dossier
TOTAL LENGTHSee the dossierEstimate scope matters
FOSSILS FOUNDChina[1]
CompareRead the dossierView the sources

MEET THE ANIMAL

Meet Chilantaisaurus

Chilantaisaurus was a very large predatory dinosaur from Inner Mongolia in China. Its known material includes an upper-arm bone, part of the pelvis and hindlimb bones. These fossils help place it among the two-legged meat-eating dinosaurs. They do not supply a complete skull and body that can simply be measured from nose to tail. [D2]

Its rock formation has a complicated dating history. Regional evidence places the deposits after an older underlying volcanic layer, but a date inferred for another fossil locality is not automatically this animal's exact age. Rocks from nearby places can have different histories. A regional age estimate therefore leaves some uncertainty about exactly when Chilantaisaurus lived. [D3]

The name also needs care. Fossils once called Chilantaisaurus maortuensis are now treated as Shaochilong. Those remains preserve different parts of the skeleton, so comparing them requires more than a shared old label. The fossils of Shaochilong do not supply Chilantaisaurus with a missing skull. [D2]

PREHISTORIC ANIMAL DOSSIER

A life in profile.

The animal, the evidence, and the questions still open.

A 580 mm humerus anchors the revised type identity. Associated hindlimbs indicate great size, but excluded teeth and vertebrae cannot supply a securely identified skull or skeleton. [D1]

Profile scope: Genus profile restricted to C. tashuikouensis at Tashuikou. Former C. maortuensis is treated separately as Shaochilong; disputed nonoverlap is conservatively reserved. [D2]

Time
Late Cretaceous
Fossil locations in this exhibit
China
How to read the evidence

Source supported identifies a description documented by the cited source. Inferred marks a reconstruction or functional estimate. Debated marks competing interpretations. Not established means the sources reviewed for this dossier do not support a firm conclusion; it does not mean a behavior never occurred.

A size reference is an estimate, not a population range. Nesting evidence does not by itself establish courtship, mate choice, or lifelong pairing.

Body length

Not established

Not established here

Focused searches did not locate a specimen-scoped whole-body length calculation in the inspected skeletal revision. Its 1,190 mm femur is a limb measurement, not total body length. [D1]

Body mass

Inferred

About 3.59 tonnes; associated-femur model

The 2014 table models IVPP V2884 at 3,590 kg from measured femoral circumference. That femur is associated type-series material, not the lectotype humerus; life stage remains unverified. [D4]

Diet

Inferred

Carnivory inferred comparatively

Theropod relationships support predatory feeding as a comparative interpretation. The historically associated tooth was excluded, so it is not secure direct evidence of this species’ dentition or meals. [D1]

Habitat & fossil setting

Source supported

Ulansuhai deposits; stage uncertain

The Inner Mongolian formation is regionally constrained as post-Cenomanian by underlying basalt. The more specific Sinocephale locality age does not directly date the Tashuikou animal; stage uncertainty remains. [D3]

Movement

Inferred

Bipedal reconstruction from hindlimbs

Large femora, tibiae and a narrow metatarsus support a two-legged theropod reconstruction. Missing axial and cranial regions prevent a complete measured posture or speed estimate. [D1]

Distinctive anatomy

Source supported

Very large humerus and associated leg bones

The designated lectotype is the right humerus, IVPP V2884.1. The remaining limb elements probably belong to the same animal, but that association is an interpretation. [D1]

Reproduction & life together

Reproduction & nesting

Not established

Not established here

Focused searches did not establish securely assigned eggs, embryos, nests, clutch size, incubation or parental care. Broader theropod evidence cannot identify this genus’s reproductive habits.

Courtship & mating

Not established

Not established here

No inspected source establishes sexual differences or display structures. A restored head cannot supply horn, crest or courtship evidence.

Social behavior

Not established

Not established here

A probably associated type series is insufficient to establish herd structure, cooperative hunting or family behavior. Focused searches found no securely attributed behavioral assemblage. [D1]

Dossier research & sources

Sources and inspection notes for the claims in this profile.

  1. The anatomy and systematic position of the theropod dinosaur Chilantaisaurus tashuikouensis Hu, 1964 from the Early Cretaceous of Alanshan, People’s Republic of ChinaGeological Magazine; Benson & Xu (2008) · Accessed 2026-10-02Original twelve-page PDF inspected: lectotype humerus, probably associated paralectotypes, excluded tooth/caudals, large limb dimensions and uncertain historical formation age. · Inspected: page
  2. The osteology of Shaochilong maortuensis, a carcharodontosaurid (Dinosauria: Theropoda) from the Late Cretaceous of AsiaZootaxa; Brusatte and colleagues (2010) · Accessed 2026-10-02Original full PDF inspected, especially pp.37–38: former C. maortuensis is Shaochilong; nonoverlapping remains prevent direct comparison, although contrasting affinities make generic identity unlikely. · Inspected: page
  3. Description and revised diagnosis of Asia’s first recorded pachycephalosaurid, Sinocephale bexelli gen. nov., from the Upper Cretaceous of Inner Mongolia, ChinaCanadian Journal of Earth Sciences; Evans, Brown, You & Campione (2021) · Accessed 2026-10-02Original author accepted manuscript inspected: Ulansuhai regional chronology from underlying basalt; locality-specific Sinocephale age inference is not directly transferred to Chilantaisaurus. · Inspected: page
  4. Rates of dinosaur body mass evolution indicate 170 million years of sustained ecological innovation on the avian stem lineagePLOS Biology; Benson and colleagues (2014) · Accessed 2026-10-02Original supplementary mass XLS inspected: C. tashuikouensis IVPP V2884, femur 1,190 mm, measured circumference 432 mm, mass model 3,590.39 kg; maturity not demonstrated by the row. · Inspected: page

THE STORY IN THE FOSSILS

Meet Chilantaisaurus.

The historical name Chilantaisaurus maortuensis became Shaochilong. The two type series do not overlap anatomically; published contrasting affinities argue against synonymy, but the unresolved comparison is retained in the duplicate guard. [2]

A regional date is not an individual date: the 2021 geological review distinguishes different Ulansuhai localities. The catalog therefore avoids a precise numerical age for the Tashuikou specimen. [3]

A note on scale and time

The dossier identifies the scope of each reference estimate. A mount, an individual fossil and a species-wide adult range are different measurements. Comparison metrics remain unavailable where adult scope has not been established. Unknown does not mean zero.

Sources & editorial notes

Sources support the stated claims and scopes. Refer to the evidence notes for uncertainty.

  1. The anatomy and systematic position of the theropod dinosaur Chilantaisaurus tashuikouensis Hu, 1964 from the Early Cretaceous of Alanshan, People’s Republic of ChinaGeological Magazine; Benson & Xu (2008) · Accessed 2026-10-02Original twelve-page PDF inspected: lectotype humerus, probably associated paralectotypes, excluded tooth/caudals, large limb dimensions and uncertain historical formation age. · Inspected: page
  2. The osteology of Shaochilong maortuensis, a carcharodontosaurid (Dinosauria: Theropoda) from the Late Cretaceous of AsiaZootaxa; Brusatte and colleagues (2010) · Accessed 2026-10-02Original full PDF inspected, especially pp.37–38: former C. maortuensis is Shaochilong; nonoverlapping remains prevent direct comparison, although contrasting affinities make generic identity unlikely. · Inspected: page
  3. Description and revised diagnosis of Asia’s first recorded pachycephalosaurid, Sinocephale bexelli gen. nov., from the Upper Cretaceous of Inner Mongolia, ChinaCanadian Journal of Earth Sciences; Evans, Brown, You & Campione (2021) · Accessed 2026-10-02Original author accepted manuscript inspected: Ulansuhai regional chronology from underlying basalt; locality-specific Sinocephale age inference is not directly transferred to Chilantaisaurus. · Inspected: page
  4. Rates of dinosaur body mass evolution indicate 170 million years of sustained ecological innovation on the avian stem lineagePLOS Biology; Benson and colleagues (2014) · Accessed 2026-10-02Original supplementary mass XLS inspected: C. tashuikouensis IVPP V2884, femur 1,190 mm, measured circumference 432 mm, mass model 3,590.39 kg; maturity not demonstrated by the row. · Inspected: page

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