crâne

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386 image(s) · 29 Actualités

Galerie d'images

Skull of Saichania, Warsaw Museum of Evolution

Skull of Saichania, Warsaw Museum of Evolution

musée Saichania évolution crâne
Skull of Oohkotokia horneri, gen. et sp. nov. (MOR 433, holotype)

Skull of Oohkotokia horneri, gen. et sp. nov. (MOR 433, holotype)

holotype Oohkotokia crâne
The incomplete skull and vertebrae of the holotype of Omphalosaurus nevadanus, seen in dorsal (left) and ventral view (right). This image was derived by combining plates 8 and 9 of Merriam (1906), done by an uncredited artist.
Legend:

A - angular
D - dentary
Pl - palatine
Pt - pterygoid
Sa - surangular
Sp - splenial
V - vertebrae
a, b, c - "doubtful elements"

The incomplete skull and vertebrae of the holotype of Omphalosaurus nevadanus, seen in dorsal (left) and ventral view (right). This image was derived by combining plates 8 and 9 of Merriam (1906), done by an uncredited artist. Legend: A - angular D - dentary Pl - palatine Pt - pterygoid Sa - surangular Sp - splenial V - vertebrae a, b, c - "doubtful elements"

holotype Merriamia crâne
Restored Placochelys placodonta skull at the Museum für Naturkunde, Berlin.

Restored Placochelys placodonta skull at the Museum für Naturkunde, Berlin.

musée Placochelyidae Placochelys crâne
Comparison of cranial features between closely related southern Laramidian taxa; (A), Akainacephalus johnsoni (UMNH VP 20202) from the Late Cretaceous Kaiparowits Formation of Utah; and (B), Nodocephalosaurus kirtlandensis (SMP VP-900) from the Late Cretaceous Kirtland Formation of New Mexico, in left lateral views. Various synapomorphies are shared with N. kirtlandensis (highlighted in black and white arrows) and includes “flaring nostrils”; enlarged, laterally projecting, loreal osteoderms that are situated directly dorsal to the external nares. Other synapomorphies include pyramid-shaped nasal and frontal osteoderms positioned on the dorsal regions of the skull. A number of significant differences have been observed between both specimens; in A. johnsoni, the anterior, and posterior supraorbital bosses form an enlarged element that is somewhat backswept, whereas in N. kirtlandensis, the posterior and anterior supraorbital bosses are clearly defined as individual osteoderms, and are much smaller in size. Additionally, the squamosal horn in Akainacephalus is very small but is prominent and tetrahedrally shaped in Nodocephalosaurus. The quadratojugal horn in Akainacephalus is massive, has a subtriangular morphology in lateral view and projects almost entirely ventral, whereas in Nodocephalosaurus, the quadratojugal horn is smaller and has a typical fin-shaped morphology. Study sites: asob, anterior supraorbital boss; ext naris, external naris; laca, lacrimal caputegulum; loca, loreal caputegulum; naca, nasal caputegulae; orb, orbit; psob, posterior supraorbital boss; qjh, quadratojugal horn; sqh, squamosal horn.

Comparison of cranial features between closely related southern Laramidian taxa; (A), Akainacephalus johnsoni (UMNH VP 20202) from the Late Cretaceous Kaiparowits Formation of Utah; and (B), Nodocephalosaurus kirtlandensis (SMP VP-900) from the Late Cretaceous Kirtland Formation of New Mexico, in left lateral views. Various synapomorphies are shared with N. kirtlandensis (highlighted in black and white arrows) and includes “flaring nostrils”; enlarged, laterally projecting, loreal osteoderms that are situated directly dorsal to the external nares. Other synapomorphies include pyramid-shaped nasal and frontal osteoderms positioned on the dorsal regions of the skull. A number of significant differences have been observed between both specimens; in A. johnsoni, the anterior, and posterior supraorbital bosses form an enlarged element that is somewhat backswept, whereas in N. kirtlandensis, the posterior and anterior supraorbital bosses are clearly defined as individual osteoderms, and are much smaller in size. Additionally, the squamosal horn in Akainacephalus is very small but is prominent and tetrahedrally shaped in Nodocephalosaurus. The quadratojugal horn in Akainacephalus is massive, has a subtriangular morphology in lateral view and projects almost entirely ventral, whereas in Nodocephalosaurus, the quadratojugal horn is smaller and has a typical fin-shaped morphology. Study sites: asob, anterior supraorbital boss; ext naris, external naris; laca, lacrimal caputegulum; loca, loreal caputegulum; naca, nasal caputegulae; orb, orbit; psob, posterior supraorbital boss; qjh, quadratojugal horn; sqh, squamosal horn.

Mexique Kaiparowits Kirtland Crétacé +6
Riojasaurus skull cast, Copenhagen.

Riojasaurus skull cast, Copenhagen.

moulage Riojasauridae Riojasaurus crâne
Skull of Pistosaurus longaevus (cast - USNM 16107) in right, left and posterior views.
Taxons Pistosaurus

Skull of Pistosaurus longaevus (cast - USNM 16107) in right, left and posterior views.

moulage Pistosauria Pistosauridae crâne
Skull of Pistosaurus longaevus (cast - USNM 16107) in right, left and posterior views.
Taxons Pistosauridae

Skull of Pistosaurus longaevus (cast - USNM 16107) in right, left and posterior views.

moulage Pistosauria Pistosauridae crâne
Skull replica of Vagaceratops at Canadian Museum of Nature

Skull replica of Vagaceratops at Canadian Museum of Nature

musée Vagaceratops crâne
Skull cast of Anchiceratops ornatus (original specimen: TMP 1983.001.0001) on display at the University of Michigan Museum of Natural History.

Skull cast of Anchiceratops ornatus (original specimen: TMP 1983.001.0001) on display at the University of Michigan Museum of Natural History.

musée moulage spécimen Anchiceratops +1
Cranial remains of Arthropterygius chrisorum CCMGE 17–44/13328 (A–J) and PMO 222.669 (L, M).

(A, B) Right postfrontal in ventral (A) and dorsal (B) views. (C) Left lateral view on articulated postfrontal, prefrontal and nasal. (D) Left prefrontal in ventral view. (E, F) Right prefrontal in ventral (E) and dorsal (F) views. (G, H) left nasal in dorsal (G) and ventral (H) views. (I, J) Left jugal in medial (I) and lateral (J) views. (K) Cranial reconstruction, showing the depicted elements (colored). (L, M) oblique dorsal view and interpretation of sutures of the skull roof of PMO 222.669. Abbreviations: ffr, facet for the frontal; fnas, facet of the nasal; fpo, facet for the postorbital; fpref, facet for the prefrontal; fqj, facet for the quadratojugal; fsut, facet for the supratemporal; lw, lateral wing of the nasal lamella; nas, nasal; par, parietal; pf, parietal foramen; pref, prefrontal; sut, supratemporal. Both scale bars represent 10 cm.

Cranial remains of Arthropterygius chrisorum CCMGE 17–44/13328 (A–J) and PMO 222.669 (L, M). (A, B) Right postfrontal in ventral (A) and dorsal (B) views. (C) Left lateral view on articulated postfrontal, prefrontal and nasal. (D) Left prefrontal in ventral view. (E, F) Right prefrontal in ventral (E) and dorsal (F) views. (G, H) left nasal in dorsal (G) and ventral (H) views. (I, J) Left jugal in medial (I) and lateral (J) views. (K) Cranial reconstruction, showing the depicted elements (colored). (L, M) oblique dorsal view and interpretation of sutures of the skull roof of PMO 222.669. Abbreviations: ffr, facet for the frontal; fnas, facet of the nasal; fpo, facet for the postorbital; fpref, facet for the prefrontal; fqj, facet for the quadratojugal; fsut, facet for the supratemporal; lw, lateral wing of the nasal lamella; nas, nasal; par, parietal; pf, parietal foramen; pref, prefrontal; sut, supratemporal. Both scale bars represent 10 cm.

écaille Arthropterygius crâne
Skull of Lesothosaurus - ornithischian dinosaur
Taxons Stormbergia

Skull of Lesothosaurus - ornithischian dinosaur

Dinosauria Lesothosauria Ornithischia Stormbergia +1
The nodosaurid dinosaur, Glyptodontopelta is mostly known from isolated osteoderms ("armor plates"). The specimen SMP VP-1580 (State Museum of Pennysylvania) is however, the most complete known specimen, comprising parts of the skull, hundreds of osteoderms and fragments. This specimen was discovered in 2003 by Warwick Fowler, in the Naashoibito Member of the Ojo Alamo Formation (Maatrichtian, Late Cretaceous) of the San Juan Basin, New Mexico, during an expedition led by Dr. Robert Sullivan.

The nodosaurid dinosaur, Glyptodontopelta is mostly known from isolated osteoderms ("armor plates"). The specimen SMP VP-1580 (State Museum of Pennysylvania) is however, the most complete known specimen, comprising parts of the skull, hundreds of osteoderms and fragments. This specimen was discovered in 2003 by Warwick Fowler, in the Naashoibito Member of the Ojo Alamo Formation (Maatrichtian, Late Cretaceous) of the San Juan Basin, New Mexico, during an expedition led by Dr. Robert Sullivan.

armure musée Mexique Denver +9
Reconstruction and restoration of the skull of Eolambia.

(A) Skull reconstruction of Eolambia in left lateral view by the lead author. Bones in white are unknown, bones in dark grey are based primarily upon the adult holotype (CEUM 9758) or paratype (CEUM 5212), and bones in light grey are based primarily upon juvenile elements from the Eo2 and WS8 bonebeds. Sutures and points of contact between bones are marked in black. Scale bar equals 10 cm; scale is calibrated with the dentary of CEUM 9758. (B) Life restoration of the head of Eolambia by Lukas Panzarin. Abbreviations: an, angular; d, dentary; f, frontal; j, jugal; l, lacrimal; mx, maxilla; na, nasal; pd, predentary; pmx, premaxilla; po, postorbital; prf, prefrontal; q, quadrate; qj, quadratojugal; sa, surangular; sq, squamosal.

Reconstruction and restoration of the skull of Eolambia. (A) Skull reconstruction of Eolambia in left lateral view by the lead author. Bones in white are unknown, bones in dark grey are based primarily upon the adult holotype (CEUM 9758) or paratype (CEUM 5212), and bones in light grey are based primarily upon juvenile elements from the Eo2 and WS8 bonebeds. Sutures and points of contact between bones are marked in black. Scale bar equals 10 cm; scale is calibrated with the dentary of CEUM 9758. (B) Life restoration of the head of Eolambia by Lukas Panzarin. Abbreviations: an, angular; d, dentary; f, frontal; j, jugal; l, lacrimal; mx, maxilla; na, nasal; pd, predentary; pmx, premaxilla; po, postorbital; prf, prefrontal; q, quadrate; qj, quadratojugal; sa, surangular; sq, squamosal.

os écaille holotype juvénile +2
Type skull of Pentaceratops sternbergii, American Museum of Natural History # AMNH6325

Type skull of Pentaceratops sternbergii, American Museum of Natural History # AMNH6325

musée Pentaceratops crâne
Figure description from the paper: "The segmented model of right lateral side of the skull of mixosaurid ichthyosaur Phalarodon fraasi (Merriam, 1910) PMO 235.393, from the Botneheia Formation, Middle Triassic of the Isfjorden area in Spitsbergen, Svalbard."
References:

Roberts, A.J.; Engelschiøn, V.S.; Hurum, J.H. (2022). "First three-dimensional skull of the Middle Triassic mixosaurid ichthyosaur Phalarodon fraasi from Svalbard, Norway". Acta Palaeontologica Polonica 67 (1): 51–62. DOI:https://doi.org/10.4202/app.00915.2021.
Taxons Contectopalatus

Figure description from the paper: "The segmented model of right lateral side of the skull of mixosaurid ichthyosaur Phalarodon fraasi (Merriam, 1910) PMO 235.393, from the Botneheia Formation, Middle Triassic of the Isfjorden area in Spitsbergen, Svalbard." References: Roberts, A.J.; Engelschiøn, V.S.; Hurum, J.H. (2022). "First three-dimensional skull of the Middle Triassic mixosaurid ichthyosaur Phalarodon fraasi from Svalbard, Norway". Acta Palaeontologica Polonica 67 (1): 51–62. DOI:https://doi.org/10.4202/app.00915.2021.

description Norvège Trias moyen Trias +7
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Actualités

Un fossile vieux de 250 millions d'années révèle les origines de l'audition des mammifères
os mâchoire fossile mammifères crâne
L’audition sensible pourrait avoir évolué chez les ancêtres des mammifères bien plus tôt que ne le croyaient les scientifiques. En modélisant la façon dont le son se déplaçait dans le crâne de Thrinaxodon, un prédécesseur mammifère vieux de 250 millions d'années, les chercheurs ont découvert qu'il utilisait probablement un tympan précoce pour entendre les sons aériens. Cela remet en question l’idée répandue selon laquelle ces animaux « écoutaient » principalement à travers leurs mâchoires ou leurs os. Les résultats révèlent qu’une caractéristique clé de l’audition des mammifères modernes prenait déjà forme au plus profond de la préhistoire.
20/01/2026 sciencedaily ⚙ Traduction automatique
Anurognathus: Beast of the Week
Anurognathus : la bête de la semaine
Allemagne Jurassique Jurassique supérieur Anurognathus Pterosauria crâne
Cette semaine, nous allons découvrir un petit ptérosaure unique, Anurognathus ammoni !  Anurognathus vivait dans ce qui est aujourd'hui l'Allemagne à la fin du Jurassique, il y a environ 150 millions d'années.  Il était minuscule, avait une envergure de 35,5 cm (14 pouces) et aurait probablement mangé des insectes.  Son nom de genre se traduit par "Frog Jaw" puisque son crâne ressemblait à celui d'une grenouille, étant extrêmement émoussé avec une bouche large.  Reconstitution à l'aquarelle d'Anurognathus ammoni par Christopher DiPiazza.Sku d'Anurognathus
14/12/2025 prehistoricbeastoftheweek ⚙ Traduction automatique
Un mini-prédateur vieux de 242 millions d'années change l'évolution du lézard
membre dent prédateur fossile évolution nouvelle espèce crâne
Un minuscule fossile du Devon vieux de 242 millions d’années bouleverse les hypothèses des scientifiques sur les premiers membres de la lignée des lézards. Au lieu des charnières du crâne et des dents du palais typiques des lézards et des serpents modernes, cette ancienne créature présente un mélange surprenant de traits primitifs et inhabituels, ainsi que des dents étonnamment grandes en forme de lame. Les scans synchrotron haute résolution ont révélé des détails invisibles à l'œil nu, aidant ainsi les chercheurs à nommer la nouvelle espèce Agriodontosaurus helsbypetrae
30/11/2025 sciencedaily ⚙ Traduction automatique
Les humains ont évolué plus vite que n’importe quel autre singe
croissance évolution crâne
Les scientifiques de l'UCL ont découvert que les crânes humains évoluaient beaucoup plus rapidement que ceux des autres singes, reflétant les forces puissantes qui conduisent la croissance de notre cerveau et l'aplatissement de notre visage. En comparant des modèles 3D de crânes de singes, ils ont montré que les humains changeaient environ deux fois plus que prévu. Les résultats suggèrent que des facteurs cognitifs et sociaux, et pas seulement l’intelligence, ont influencé notre évolution.
29/10/2025 sciencedaily-human-evo ⚙ Traduction automatique
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