os

Partie anatomique

62 image(s) · 32 Actualités

Galerie d'images

Main evolutionary steps proposed for the morphofunctional and postural changes of the sauropod pedes. (A) Sauropod body mass through time (in metric tons) based on the sauropod body mass estimations of (41) (NB: data lacking for the second half of the Upper Cretaceous so illustrated here faded, in continuity with the data recorded in the Cretaceous). Schematic outlines of selected large specimens illustrated in the curve, including (from left to right) P. engelhardti, Vulcanodon karibaensis, R. brownei, G. brancai, Cedarosaurus weiskopfae, and Notocolossus gonzalezparejasi. (B) Projected evolutionary changes occurring in the sauropod pes associated with trend in body mass, including 1, skeletal and functional digitigrade pedal posture among basal non-sauropod sauropodomorphs with an incipient soft tissue pad (ISP) (see figs. S34 and S35); 2 and 3, expansion of a well-developed soft tissue pad beneath the elevated pedal bones (SP), resulting in a functionally plantigrade pes + retention of skeletal posture within a range of digitigrady; 4, retention of a soft tissue pad and yet undetermined trend toward more elevated bones; 5, conservation of the neomorphic soft tissue pad within all lineages. Selected examples of well-preserved non-sauropod sauropodomorph and sauropod pedal tracks illustrated above the trends, including (from left to right) Evazoum siriguii; Pseudotetrasauropus bipedoida, Eosauropus isp., Lavinipes cheminii; Kalosauropus pollex, Liujianpus shunan, Polyonyx gomesi; Parabrontopodus mcintoshi; Brontopodus birdi; Titanopodus mendozensis; and unnamed Asian sauropod track. Source of adapted drawing and notes are listed in table S9 and data S2.
Taxons Evazoum

Main evolutionary steps proposed for the morphofunctional and postural changes of the sauropod pedes. (A) Sauropod body mass through time (in metric tons) based on the sauropod body mass estimations of (41) (NB: data lacking for the second half of the Upper Cretaceous so illustrated here faded, in continuity with the data recorded in the Cretaceous). Schematic outlines of selected large specimens illustrated in the curve, including (from left to right) P. engelhardti, Vulcanodon karibaensis, R. brownei, G. brancai, Cedarosaurus weiskopfae, and Notocolossus gonzalezparejasi. (B) Projected evolutionary changes occurring in the sauropod pes associated with trend in body mass, including 1, skeletal and functional digitigrade pedal posture among basal non-sauropod sauropodomorphs with an incipient soft tissue pad (ISP) (see figs. S34 and S35); 2 and 3, expansion of a well-developed soft tissue pad beneath the elevated pedal bones (SP), resulting in a functionally plantigrade pes + retention of skeletal posture within a range of digitigrady; 4, retention of a soft tissue pad and yet undetermined trend toward more elevated bones; 5, conservation of the neomorphic soft tissue pad within all lineages. Selected examples of well-preserved non-sauropod sauropodomorph and sauropod pedal tracks illustrated above the trends, including (from left to right) Evazoum siriguii; Pseudotetrasauropus bipedoida, Eosauropus isp., Lavinipes cheminii; Kalosauropus pollex, Liujianpus shunan, Polyonyx gomesi; Parabrontopodus mcintoshi; Brontopodus birdi; Titanopodus mendozensis; and unnamed Asian sauropod track. Source of adapted drawing and notes are listed in table S9 and data S2.

os tissus Crétacé spécimen +6
Main evolutionary steps proposed for the morphofunctional and postural changes of the sauropod pedes. (A) Sauropod body mass through time (in metric tons) based on the sauropod body mass estimations of (41) (NB: data lacking for the second half of the Upper Cretaceous so illustrated here faded, in continuity with the data recorded in the Cretaceous). Schematic outlines of selected large specimens illustrated in the curve, including (from left to right) P. engelhardti, Vulcanodon karibaensis, R. brownei, G. brancai, Cedarosaurus weiskopfae, and Notocolossus gonzalezparejasi. (B) Projected evolutionary changes occurring in the sauropod pes associated with trend in body mass, including 1, skeletal and functional digitigrade pedal posture among basal non-sauropod sauropodomorphs with an incipient soft tissue pad (ISP) (see figs. S34 and S35); 2 and 3, expansion of a well-developed soft tissue pad beneath the elevated pedal bones (SP), resulting in a functionally plantigrade pes + retention of skeletal posture within a range of digitigrady; 4, retention of a soft tissue pad and yet undetermined trend toward more elevated bones; 5, conservation of the neomorphic soft tissue pad within all lineages. Selected examples of well-preserved non-sauropod sauropodomorph and sauropod pedal tracks illustrated above the trends, including (from left to right) Evazoum siriguii; Pseudotetrasauropus bipedoida, Eosauropus isp., Lavinipes cheminii; Kalosauropus pollex, Liujianpus shunan, Polyonyx gomesi; Parabrontopodus mcintoshi; Brontopodus birdi; Titanopodus mendozensis; and unnamed Asian sauropod track. Source of adapted drawing and notes are listed in table S9 and data S2.
Taxons Kalosauropus

Main evolutionary steps proposed for the morphofunctional and postural changes of the sauropod pedes. (A) Sauropod body mass through time (in metric tons) based on the sauropod body mass estimations of (41) (NB: data lacking for the second half of the Upper Cretaceous so illustrated here faded, in continuity with the data recorded in the Cretaceous). Schematic outlines of selected large specimens illustrated in the curve, including (from left to right) P. engelhardti, Vulcanodon karibaensis, R. brownei, G. brancai, Cedarosaurus weiskopfae, and Notocolossus gonzalezparejasi. (B) Projected evolutionary changes occurring in the sauropod pes associated with trend in body mass, including 1, skeletal and functional digitigrade pedal posture among basal non-sauropod sauropodomorphs with an incipient soft tissue pad (ISP) (see figs. S34 and S35); 2 and 3, expansion of a well-developed soft tissue pad beneath the elevated pedal bones (SP), resulting in a functionally plantigrade pes + retention of skeletal posture within a range of digitigrady; 4, retention of a soft tissue pad and yet undetermined trend toward more elevated bones; 5, conservation of the neomorphic soft tissue pad within all lineages. Selected examples of well-preserved non-sauropod sauropodomorph and sauropod pedal tracks illustrated above the trends, including (from left to right) Evazoum siriguii; Pseudotetrasauropus bipedoida, Eosauropus isp., Lavinipes cheminii; Kalosauropus pollex, Liujianpus shunan, Polyonyx gomesi; Parabrontopodus mcintoshi; Brontopodus birdi; Titanopodus mendozensis; and unnamed Asian sauropod track. Source of adapted drawing and notes are listed in table S9 and data S2.

os tissus Crétacé spécimen +6
Remake of the original picture of the Drzewica Formation. Terrestrial environment of the Pliensbachian-Toarcian boundary of Fennoscandinavia  Inland environment of the  Bornholm Coast, nearby the German realm of the Ciechocinek Formation. Includes
Ciechocinek Formation (Lower Toarcian, Bones) and Drzwica Formation (Latest Pliensbachian, Footprints) Fauna
Sorthat Formation environment, fluvial influenced mainland with Cheirolepidaceae and Bennetitales as dominant flora
Dinosaurs are based on material found on various locations of Northern Germany, and Footprints of the underliying Drzewica Formation at the Holy Cross Mountains, connected with Bornholm at the time.
Dinosaur Species appeared: 

Megalosauripus isp. Large Footprints (+65 cm) found on the Drzewica Formation. There is a dorsal vertebrae on the German Margin of the Ciechocinek Formation assigend to Megalosauria (Huene, 1966).
Gravisauria spp. representing the Grimmen Sauropod reported on 2014, as a taxon related with Tazoudasaurus. Barapasaurus-like footprints are know from the Drzewica Formation.
Coelophysoidea spp. based on coeval Anchisauripus tracks from the Holy Cross Mountains.
Basal Ornithischan, related to Eocursor, based on a crouching trace (Gerard Dariusz Gierlinski, Martin G. Lockley, Grzegorz Niedźwiedzki:2009).
Massospondylidae spp. based on Otozum-like tracks.
Taxons Megalosauripus

Remake of the original picture of the Drzewica Formation. Terrestrial environment of the Pliensbachian-Toarcian boundary of Fennoscandinavia Inland environment of the Bornholm Coast, nearby the German realm of the Ciechocinek Formation. Includes Ciechocinek Formation (Lower Toarcian, Bones) and Drzwica Formation (Latest Pliensbachian, Footprints) Fauna Sorthat Formation environment, fluvial influenced mainland with Cheirolepidaceae and Bennetitales as dominant flora Dinosaurs are based on material found on various locations of Northern Germany, and Footprints of the underliying Drzewica Formation at the Holy Cross Mountains, connected with Bornholm at the time. Dinosaur Species appeared: Megalosauripus isp. Large Footprints (+65 cm) found on the Drzewica Formation. There is a dorsal vertebrae on the German Margin of the Ciechocinek Formation assigend to Megalosauria (Huene, 1966). Gravisauria spp. representing the Grimmen Sauropod reported on 2014, as a taxon related with Tazoudasaurus. Barapasaurus-like footprints are know from the Drzewica Formation. Coelophysoidea spp. based on coeval Anchisauripus tracks from the Holy Cross Mountains. Basal Ornithischan, related to Eocursor, based on a crouching trace (Gerard Dariusz Gierlinski, Martin G. Lockley, Grzegorz Niedźwiedzki:2009). Massospondylidae spp. based on Otozum-like tracks.

os Allemagne Pliensbachien Toarcien +7
Bones and remains of prehistoric animals
A massive marine lizard and apex predator, growing to length of 14 m (46 ft).[1]

Bones and remains of prehistoric animals A massive marine lizard and apex predator, growing to length of 14 m (46 ft).[1]

os prédateur Tylosaurus
Reconstruction of Tuebingosaurus maierfritzorum gen. et sp. nov. as a quadruped dinosaur, using the outline of Riojasaurus as a base ‒ next to the silhouette of Friedrich von Huene. The drawing of the bones is based on and modified from the original illustrations of specimen “GPIT IV” in von Huene (1932, pl. 38) that have been replicated in the literature. The right fibula is marked in grey as it was found nearby with similar measurements to the left fibula and has been assumed to be part of the same individual.
Taxons Tuebingosaurus

Reconstruction of Tuebingosaurus maierfritzorum gen. et sp. nov. as a quadruped dinosaur, using the outline of Riojasaurus as a base ‒ next to the silhouette of Friedrich von Huene. The drawing of the bones is based on and modified from the original illustrations of specimen “GPIT IV” in von Huene (1932, pl. 38) that have been replicated in the literature. The right fibula is marked in grey as it was found nearby with similar measurements to the left fibula and has been assumed to be part of the same individual.

os dessin spécimen Dinosauria +2
Holotype fossils of Glacialisaurus (PR 1823); metatarsals, tibia, fibula, ankle bones
Taxons Glacialisaurus

Holotype fossils of Glacialisaurus (PR 1823); metatarsals, tibia, fibula, ankle bones

os fossile holotype Glacialisaurus
Alvarezsauroid theropod Linhenykus monodactylus Xu, Sullivan, Pittman, Choiniere, Hone, Upchurch, Tan, Xiao, Tan, and Han, 2011a,

Bayan Mandahu (“Gate Locality”), Late Cretaceous (Campanian), holo−type (IVPP V17608). Skeletal silhouette showing preserved bones (missing portions shown in grey).
Taxons Linhenykus

Alvarezsauroid theropod Linhenykus monodactylus Xu, Sullivan, Pittman, Choiniere, Hone, Upchurch, Tan, Xiao, Tan, and Han, 2011a, Bayan Mandahu (“Gate Locality”), Late Cretaceous (Campanian), holo−type (IVPP V17608). Skeletal silhouette showing preserved bones (missing portions shown in grey).

os Campanien Crétacé Crétacé supérieur +1
Skeleton of Yamaceratops dorngobiensis (MPC-D 100/553) in right dorsolateral view. (A) Photograph; (B) Interpretive drawing. Bones are bounded by solid lines and colored beige; the matrix is gray. Shaded areas represent the broken surface of bones. Abbreviations: cd, caudal vertebrae; dr, dorsal ribs; dv, dorsal vertebrae; f, femur; fi, fibula; h, humerus; L, bone on the left side; p, isolated parietal; pp, pedal phalanges; R, bone on the right side; ra, radius; sk, skull; sv, sacral vertebrae; ti, tibia; u, ulna; il, ilium; is, ischium.
Taxons Yamaceratops

Skeleton of Yamaceratops dorngobiensis (MPC-D 100/553) in right dorsolateral view. (A) Photograph; (B) Interpretive drawing. Bones are bounded by solid lines and colored beige; the matrix is gray. Shaded areas represent the broken surface of bones. Abbreviations: cd, caudal vertebrae; dr, dorsal ribs; dv, dorsal vertebrae; f, femur; fi, fibula; h, humerus; L, bone on the left side; p, isolated parietal; pp, pedal phalanges; R, bone on the right side; ra, radius; sk, skull; sv, sacral vertebrae; ti, tibia; u, ulna; il, ilium; is, ischium.

os humérus dessin Yamaceratops +2
Right dentary in (A), medial; (B), dorsal; and (C) lateral views. Dashed black lines represent approximate contours of the missing areas. Dashed red lines indicate the distinctive banding pattern in the opal used to estimate the extent of the missing area. (D–F) Three-dimensional renders of the posterior dentary fragment in (D) lingual view showing erupted (blue) and developing germ teeth (pink); (E) Same as (D) but with dentary removed; (F) dorsal (occlusal) view of tooth row. (G-J) Three-dimensional render of the best-preserved tooth in (G) mesial, (H) lingual, (I) distal, and (J) labial views. (K) MicroCT scan of the posterior dentary fragment in axial view showing preservation of cancellous bone. Abbreviations: cab, cancellous bone; cr, tooth crown. Photo credit: Phil Bell.
Taxons Weewarrasaurus

Right dentary in (A), medial; (B), dorsal; and (C) lateral views. Dashed black lines represent approximate contours of the missing areas. Dashed red lines indicate the distinctive banding pattern in the opal used to estimate the extent of the missing area. (D–F) Three-dimensional renders of the posterior dentary fragment in (D) lingual view showing erupted (blue) and developing germ teeth (pink); (E) Same as (D) but with dentary removed; (F) dorsal (occlusal) view of tooth row. (G-J) Three-dimensional render of the best-preserved tooth in (G) mesial, (H) lingual, (I) distal, and (J) labial views. (K) MicroCT scan of the posterior dentary fragment in axial view showing preservation of cancellous bone. Abbreviations: cab, cancellous bone; cr, tooth crown. Photo credit: Phil Bell.

os dent Weewarrasaurus
Figure 1, 1a. Outer and oral aspects of the imperfect dentary bone of Sarcolestes Leedsi, from the Oxford Clay of Peterborough. 2/3 nat size. s = symphysis. Figure 1b. A single tooth of the former. 3/1 nat size. Figure 2, 2a. Outer aspect and quadratic cavity of the hinder region of the same jaw. 2/3 nat size. Figure 3. A single tooth of Priodontognathus Phillipsi, 3/1 nat size, shown for purposes of comparison. Specimen in the Woodwardian Museum, Cambridge.
Taxons Sarcolestes

Figure 1, 1a. Outer and oral aspects of the imperfect dentary bone of Sarcolestes Leedsi, from the Oxford Clay of Peterborough. 2/3 nat size. s = symphysis. Figure 1b. A single tooth of the former. 3/1 nat size. Figure 2, 2a. Outer aspect and quadratic cavity of the hinder region of the same jaw. 2/3 nat size. Figure 3. A single tooth of Priodontognathus Phillipsi, 3/1 nat size, shown for purposes of comparison. Specimen in the Woodwardian Museum, Cambridge.

os dent musée Oxford Clay +3
Title: The dinosaur book : the ruling reptiles and their relatives
Identifier: bookruli00colb (find matches)
Year: 1951 (1950s)
Authors: Colbert, Edwin H. (Edwin Harris), 1905-2001; Knight, Charles Robert, 1874-1953; American Museum of Natural History
Subjects: Dinosaurs; Reptiles, Fossil
Publisher: New York : Published for the American Museum of Natural History by McGraw-Hill
Contributing Library: American Museum of Natural History Library
Digitizing Sponsor: IMLS / LSTA / METRO

View Book Page: Book Viewer
About This Book: Catalog Entry
View All Images: All Images From Book
Click here to view book online to see this illustration in context in a browseable online version of this book.

Text Appearing Before Image: 
'
Text Appearing After Image: 
bone A typical example of the parts usually found fossilized: portions of the skeleton of a small dinosaur from Mongolia A.M.N.H. photographs One of the rarest fossils: a dino- saur egg over 60 million years old, compared with a hen's egg (left) and an alligator egg (right)

Note About Images

Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.
Taxons Oviraptor

Title: The dinosaur book : the ruling reptiles and their relatives Identifier: bookruli00colb (find matches) Year: 1951 (1950s) Authors: Colbert, Edwin H. (Edwin Harris), 1905-2001; Knight, Charles Robert, 1874-1953; American Museum of Natural History Subjects: Dinosaurs; Reptiles, Fossil Publisher: New York : Published for the American Museum of Natural History by McGraw-Hill Contributing Library: American Museum of Natural History Library Digitizing Sponsor: IMLS / LSTA / METRO View Book Page: Book Viewer About This Book: Catalog Entry View All Images: All Images From Book Click here to view book online to see this illustration in context in a browseable online version of this book. Text Appearing Before Image: ' Text Appearing After Image: bone A typical example of the parts usually found fossilized: portions of the skeleton of a small dinosaur from Mongolia A.M.N.H. photographs One of the rarest fossils: a dino- saur egg over 60 million years old, compared with a hen's egg (left) and an alligator egg (right) Note About Images Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.

os musée Mongolie fossile +4
Title: The dinosaur book : the ruling reptiles and their relatives
Identifier: bookruli00colb (find matches)
Year: 1951 (1950s)
Authors: Colbert, Edwin H. (Edwin Harris), 1905-2001; Knight, Charles Robert, 1874-1953; American Museum of Natural History
Subjects: Dinosaurs; Reptiles, Fossil
Publisher: New York : Published for the American Museum of Natural History by McGraw-Hill
Contributing Library: American Museum of Natural History Library
Digitizing Sponsor: IMLS / LSTA / METRO

View Book Page: Book Viewer
About This Book: Catalog Entry
View All Images: All Images From Book
Click here to view book online to see this illustration in context in a browseable online version of this book.

Text Appearing Before Image: 
'
Text Appearing After Image: 
bone A typical example of the parts usually found fossilized: portions of the skeleton of a small dinosaur from Mongolia A.M.N.H. photographs One of the rarest fossils: a dino- saur egg over 60 million years old, compared with a hen's egg (left) and an alligator egg (right)

Note About Images

Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.
Taxons Fenestrosaurus

Title: The dinosaur book : the ruling reptiles and their relatives Identifier: bookruli00colb (find matches) Year: 1951 (1950s) Authors: Colbert, Edwin H. (Edwin Harris), 1905-2001; Knight, Charles Robert, 1874-1953; American Museum of Natural History Subjects: Dinosaurs; Reptiles, Fossil Publisher: New York : Published for the American Museum of Natural History by McGraw-Hill Contributing Library: American Museum of Natural History Library Digitizing Sponsor: IMLS / LSTA / METRO View Book Page: Book Viewer About This Book: Catalog Entry View All Images: All Images From Book Click here to view book online to see this illustration in context in a browseable online version of this book. Text Appearing Before Image: ' Text Appearing After Image: bone A typical example of the parts usually found fossilized: portions of the skeleton of a small dinosaur from Mongolia A.M.N.H. photographs One of the rarest fossils: a dino- saur egg over 60 million years old, compared with a hen's egg (left) and an alligator egg (right) Note About Images Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.

os musée Mongolie fossile +4
Montanoceratops cerorhynchus (Brown & Schlaikjer, 1942) - fossil ceratopsian dinosaur skeleton from the Cretaceous of Montana, USA. (MOR 542, Museum of the Rockies, Bozeman, Montana, USA)
The species name is sometimes incorrectly spelled "cerorhynchos".  The original publication spells it "cerorhynchus".  The genus name is sometimes incorrectly spelled "Montanaceratops".
Ceratopsians are the "horned dinosaurs".  They were large, quadrupedal, herbivorous dinosaurs having a beaked skull and a frill - an extension of bone behind the skull that partially covered the neck.  Ceratopsian dinosaurs are known from the Jurassic and Cretaceous.  The last members of the group died out at the Cretaceous-Tertiary boundary, 65 million years ago.
This is a partial skeleton of a juvenile Montanoceratops, a ceratopsian from the near-latest Cretaceous of western North America.  This type of ceratopsian lacked facial horns.


From exhibit signage:
Sixty-eight million years ago, when the horned dinosaurs Triceratops and Torosaurus inhabited the coastal plain near the inland ocean, primitive "horned" dinosaurs named Montanoceratops lived in uplands near the young Rocky Mountains.  These little protoceratopsians fed on plants with slicing teeth and narrow beaks similar to their giant three-horned relatives.


Classification: Animalia, Chordata, Vertebrata, Reptilia, Archosauria, Dinosauria, Ornithischia, Marginocephalia, Ceratopsia, Leptoceratopsidae
Stratigraphy: St. Mary River Formation, Maastrichtian Stage, Upper Cretaceous
Locality: Little Rocky Coulee, north of the town of Cut Bank, eastern Glacier County, northwestern Montana, USA


Info. at:

en.wikipedia.org/wiki/Montanoceratops
Taxons Montanoceratops

Montanoceratops cerorhynchus (Brown & Schlaikjer, 1942) - fossil ceratopsian dinosaur skeleton from the Cretaceous of Montana, USA. (MOR 542, Museum of the Rockies, Bozeman, Montana, USA) The species name is sometimes incorrectly spelled "cerorhynchos". The original publication spells it "cerorhynchus". The genus name is sometimes incorrectly spelled "Montanaceratops". Ceratopsians are the "horned dinosaurs". They were large, quadrupedal, herbivorous dinosaurs having a beaked skull and a frill - an extension of bone behind the skull that partially covered the neck. Ceratopsian dinosaurs are known from the Jurassic and Cretaceous. The last members of the group died out at the Cretaceous-Tertiary boundary, 65 million years ago. This is a partial skeleton of a juvenile Montanoceratops, a ceratopsian from the near-latest Cretaceous of western North America. This type of ceratopsian lacked facial horns. From exhibit signage: Sixty-eight million years ago, when the horned dinosaurs Triceratops and Torosaurus inhabited the coastal plain near the inland ocean, primitive "horned" dinosaurs named Montanoceratops lived in uplands near the young Rocky Mountains. These little protoceratopsians fed on plants with slicing teeth and narrow beaks similar to their giant three-horned relatives. Classification: Animalia, Chordata, Vertebrata, Reptilia, Archosauria, Dinosauria, Ornithischia, Marginocephalia, Ceratopsia, Leptoceratopsidae Stratigraphy: St. Mary River Formation, Maastrichtian Stage, Upper Cretaceous Locality: Little Rocky Coulee, north of the town of Cut Bank, eastern Glacier County, northwestern Montana, USA Info. at: en.wikipedia.org/wiki/Montanoceratops

os musée États-Unis Crétacé +10
Muttaburrasaurus
The plants, animals and climate of the Australian continent have changed dramatically over long periods of time. Imagine this giant creature roaming the luxuriant wet forests that covered parts of the continent in the Cretaceous period, about 100-110 million years ago. The Muttaburrasaurus ambled along on all four legs or stood on its hind legs. Its large teeth were well adapted to eat tough vegetation such as the leathery foliage of the evergreen forests of Araucaria trees, ancient relatives of the bunya pine of south-eastern Queensland.
In 1963, grazier Doug Langdon discovered the fossilised bones of a dinosaur on his property near Muttaburra in central-west Queensland. It was one of the most complete dinosaur skeletons found in Australia. The bones belonged to a new species of ornithopod and palaeontologists named it Muttaburrasaurus langdoni.

Cast of Muttaburresaurus langdoni 1987 made by Queensland Museum, Brisbane National Museum of Australia
Taxons Muttaburrasaurus

Muttaburrasaurus The plants, animals and climate of the Australian continent have changed dramatically over long periods of time. Imagine this giant creature roaming the luxuriant wet forests that covered parts of the continent in the Cretaceous period, about 100-110 million years ago. The Muttaburrasaurus ambled along on all four legs or stood on its hind legs. Its large teeth were well adapted to eat tough vegetation such as the leathery foliage of the evergreen forests of Araucaria trees, ancient relatives of the bunya pine of south-eastern Queensland. In 1963, grazier Doug Langdon discovered the fossilised bones of a dinosaur on his property near Muttaburra in central-west Queensland. It was one of the most complete dinosaur skeletons found in Australia. The bones belonged to a new species of ornithopod and palaeontologists named it Muttaburrasaurus langdoni. Cast of Muttaburresaurus langdoni 1987 made by Queensland Museum, Brisbane National Museum of Australia

os musée Australie Crétacé +5
Illustration of the holotype frontal bone of Albertavenator curriei TMP 1993.105.0001 in dorsal view. Scale bar is 5mm.
Taxons Albertavenator

Illustration of the holotype frontal bone of Albertavenator curriei TMP 1993.105.0001 in dorsal view. Scale bar is 5mm.

os écaille holotype Albertavenator
Lower jaw, arm bone, and leg bone (LACM 128258 and LACM 120478) of Fruitadens haagarorum on display at the Natural History Museum of Los Angeles County.
Taxons Fruitadens

Lower jaw, arm bone, and leg bone (LACM 128258 and LACM 120478) of Fruitadens haagarorum on display at the Natural History Museum of Los Angeles County.

os musée Fruitadens
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Actualités

Mystery of Tyrannosaurus rex’s Tiny Arms May Finally Have an Answer
Le mystère des petits bras du Tyrannosaurus rex pourrait enfin avoir une réponse
os mâchoire prédateur proie Dinosauria Tyrannosaurus
Les paléontologues de l'University College de Londres et de l'Université de Cambridge affirment que les bras minuscules des grands dinosaures prédateurs ont évolué aux côtés de têtes massives et de mâchoires broyantes, ce qui suggère que les anciens prédateurs comptaient de plus en plus sur la morsure plutôt que sur la saisie de leurs proies. L’article Le mystère des petits bras du Tyrannosaurus rex pourrait enfin avoir une réponse apparaît en premier sur Sci.News : Breaking Science News.
20/05/2026 sci-news ⚙ Traduction automatique
Giant New Dinosaur Species Discovered in Thailand Reveals Hidden Diversity of Asian Titans
Une nouvelle espèce de dinosaure géant découverte en Thaïlande révèle la diversité cachée des titans asiatiques
os Thaïlande Crétacé Crétacé inférieur Dinosauria Somphospondyli Titanosauriformes découverte nouvelle espèce
Les paléontologues ont identifié un nouveau genre et une nouvelle espèce de dinosaure titanosauriforme somphospondylan - le plus grand jamais découvert en Asie du Sud-Est - à partir d'ossements fossilisés trouvés en Thaïlande, offrant ainsi une nouvelle preuve que la région abritait un groupe étonnamment diversifié d'énormes herbivores au début du Crétacé. L'article Une nouvelle espèce de dinosaure géant découverte en Thaïlande révèle la diversité cachée des titans asiatiques apparaît en premier sur Sci.News : Breaking Science News.
14/05/2026 sci-news ⚙ Traduction automatique
La paléontologie secouée par la découverte de molécules organiques dans des os de dinosaures vieux de 66 millions d'années
os collagène protéine fossile Dinosauria Edmontosaurus découverte
Les scientifiques ont découvert des preuves irréfutables selon lesquelles les fossiles de dinosaures peuvent encore contenir des traces de leurs protéines d'origine, renversant ainsi une croyance de longue date selon laquelle la fossilisation détruit toute matière organique. Dans un fossile d'Edmontosaurus remarquablement bien conservé du Dakota du Sud, les chercheurs ont détecté des restes de collagène – la principale protéine présente dans les os – à l'aide de techniques avancées, notamment la spectrométrie de masse et le séquençage des protéines.
14/05/2026 sciencedaily ⚙ Traduction automatique
Gongshuilong: Beast of the Week
Gongshuilong : Bête de la semaine
os Chine Crétacé Crétacé supérieur Gongshuilong Hadrosauria
 Aujourd'hui, nous examinons un hadrosaure récemment décrit avec un look unique, Gongshuilong fanwei ! Gongshuilong vivait dans ce qui est aujourd'hui l'est de la Chine, à la fin du Crétacé, il y a entre 68 et 66 millions d'années.  Du bec à la queue, il mesurait environ 7 m de long et aurait été un herbivore de son vivant.  Le nom du genre se traduit du mandarin par "Dragon de la rivière Gong" en référence à la rivière Gong près de l'endroit où ses os ont été découverts. Reconstruction de la vie de Gongshuilong à l'aquarelle b
10/05/2026 prehistoricbeastoftheweek ⚙ Traduction automatique
En Chine, les humains de la période glaciaire ont fabriqué des outils en pierre étonnamment avancés il y a 146 000 ans
os Chine découverte
Des scientifiques chinois ont découvert que les anciens humains fabriquaient des outils en pierre étonnamment avancés au cours d'une dure période glaciaire, il y a 146 000 ans. Les outils, créés par Homo juluensis, témoignent d'une planification minutieuse et d'une réflexion complexe plutôt que d'un simple taillage de pierres. Les chercheurs ont daté le site à l’aide de minuscules cristaux de calcite contenus dans des os d’animaux, révélant que les outils sont beaucoup plus anciens que prévu. Cette découverte remet en question l’idée selon laquelle la créativité humaine ne prospère que dans les périodes faciles et prospères.
09/05/2026 sciencedaily-paleo ⚙ Traduction automatique
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