os

Partie anatomique

68 image(s) · 40 Actualités

Galerie d'images

Bones referred to Ibirania parva, A. Middle caudal vertebra (MPMA 08-0060-07) referred to I. parva. B. Views of partial right ulna (LPP-PV-0202) of the I. parva holotype. According to Navarro et al. (2022).

Bones referred to Ibirania parva, A. Middle caudal vertebra (MPMA 08-0060-07) referred to I. parva. B. Views of partial right ulna (LPP-PV-0202) of the I. parva holotype. According to Navarro et al. (2022).

os vertèbre holotype Ibirania +1
Herbivorous dinosaur found in the Al-khoudh area.  This dinosaur is similar to the Zalmoxes and Rhabdodon dinosaurs.  The skeleton in the Bait Al Baranda Museum was assembled from bones borrowed from several museums.

Herbivorous dinosaur found in the Al-khoudh area. This dinosaur is similar to the Zalmoxes and Rhabdodon dinosaurs. The skeleton in the Bait Al Baranda Museum was assembled from bones borrowed from several museums.

os musée Dinosauria Mochlodon +3
Dinosaur Bones

Dinosaur Bones

os Sri Lanka Anzu Dinosauria
MRF 319, a partial oviraptorosaurian skeleton referred to Anzu wyliei. 
(A) Skeletal reconstruction in left lateral view, with preserved bones in gray and bones represented in other Anzu specimens in white (hatching indicates heavily reconstructed portions of the ilia of CM 78001). Middle-posterior (ninth?) cervical vertebra in (B) anterior, (C) left lateral, and (D) dorsal views. Posterior (11th?) cervical vertebra in (E) anterior, (F) left lateral, and (G) dorsal views. Posterior (12th?) cervical vertebra in (H) anterior, (I) left lateral, and (J) dorsal views. Anteroposteriorly crushed left radius in lateral (K) and anterior (L) views. Mediolaterally crushed left ulna in lateral (M) and anterior (N) views. (O) Partial left scapulocoracoid in lateral view. Dorsal rib in anterior (P) and posterior (Q) views. Abbreviations: acr, acromial process; cr, cervical rib; dip, distal processes; pat, pathology; pf, pneumatic fossa. Scale bars = 50 cm in A; 1 cm in B–Q.

MRF 319, a partial oviraptorosaurian skeleton referred to Anzu wyliei. (A) Skeletal reconstruction in left lateral view, with preserved bones in gray and bones represented in other Anzu specimens in white (hatching indicates heavily reconstructed portions of the ilia of CM 78001). Middle-posterior (ninth?) cervical vertebra in (B) anterior, (C) left lateral, and (D) dorsal views. Posterior (11th?) cervical vertebra in (E) anterior, (F) left lateral, and (G) dorsal views. Posterior (12th?) cervical vertebra in (H) anterior, (I) left lateral, and (J) dorsal views. Anteroposteriorly crushed left radius in lateral (K) and anterior (L) views. Mediolaterally crushed left ulna in lateral (M) and anterior (N) views. (O) Partial left scapulocoracoid in lateral view. Dorsal rib in anterior (P) and posterior (Q) views. Abbreviations: acr, acromial process; cr, cervical rib; dip, distal processes; pat, pathology; pf, pneumatic fossa. Scale bars = 50 cm in A; 1 cm in B–Q.

os écaille vertèbre pathologie +5
MRF 319, a partial oviraptorosaurian skeleton referred to Anzu wyliei. Skeletal reconstruction in left lateral view, with preserved bones in gray and bones represented in other Anzu specimens in white (hatching indicates heavily reconstructed portions of the ilia. Scale bar = 50 cm (19.7 in)

MRF 319, a partial oviraptorosaurian skeleton referred to Anzu wyliei. Skeletal reconstruction in left lateral view, with preserved bones in gray and bones represented in other Anzu specimens in white (hatching indicates heavily reconstructed portions of the ilia. Scale bar = 50 cm (19.7 in)

os écaille spécimen Anzu +3
Osteohistology of UALVP 59606, metatarsal IV of Citipes elegans. Overview of histological thin section of UALVP 59606 in plane-polarized (A) and cross-polarized (B) light, showing locations of close-up images. Detail (C) of cortex showing predominantly primary fibrolamellar bone with longitudinal-reticular vascularity, endosteal layer, and cyclical growth marks (arrows), under plane-polarized light. Close-up (D) of well developed endosteal layer on the medullary cavity, showing sec- ondary excavation by simple vascular canals, under cross-polarized light. Close-up (E) of tightly packed cyclical growth marks (arrows) near the periosteal surface of the cortex, under plane-polarized light. Close-up (F) of periosteal surface of cortex, showing avascular parallel-fibered bone indicating an incipient external fundamental system (double ended arrow) with three LAGs (arrows). Abbreviations: efs, incipient external fundamental system; el, endosteal lamellae; hb, Haversian bone; pfb, parallel-fibered bone; radv, radial simple vascular canal; so, secondary osteon.

Osteohistology of UALVP 59606, metatarsal IV of Citipes elegans. Overview of histological thin section of UALVP 59606 in plane-polarized (A) and cross-polarized (B) light, showing locations of close-up images. Detail (C) of cortex showing predominantly primary fibrolamellar bone with longitudinal-reticular vascularity, endosteal layer, and cyclical growth marks (arrows), under plane-polarized light. Close-up (D) of well developed endosteal layer on the medullary cavity, showing sec- ondary excavation by simple vascular canals, under cross-polarized light. Close-up (E) of tightly packed cyclical growth marks (arrows) near the periosteal surface of the cortex, under plane-polarized light. Close-up (F) of periosteal surface of cortex, showing avascular parallel-fibered bone indicating an incipient external fundamental system (double ended arrow) with three LAGs (arrows). Abbreviations: efs, incipient external fundamental system; el, endosteal lamellae; hb, Haversian bone; pfb, parallel-fibered bone; radv, radial simple vascular canal; so, secondary osteon.

os croissance Citipes Leptorhynchos +1
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.

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
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Actualités

Cet étrange serpent ancien se cachait dans un musée depuis des décennies
os musée fossile découverte
Un étrange petit fossile de serpent trouvé sur la côte sud de l’Angleterre a enfin révélé ses secrets, plus de 40 ans après sa découverte. Le nouveau Paradoxophidion richardoweni vivait il y a environ 37 millions d’années, à une époque où la Grande-Bretagne était plus chaude et regorgeait de reptiles. Bien que connu uniquement à partir de minuscules os de la colonne vertébrale, ce « serpent paradoxal » présente un mélange surprenant de traits observés chez les serpents modernes, le plaçant près des racines mêmes du groupe de serpents le plus diversifié d’aujourd’hui.
31/12/2025 sciencedaily ⚙ Traduction automatique
Des os de dinosaures découverts presque les uns sur les autres en Transylvanie
os bassin Roumanie fossile Dinosauria Titanosauria squelette
Des scientifiques explorant le bassin de Hațeg en Roumanie ont découvert l’un des sites de fossiles de dinosaures les plus denses jamais découverts, avec des os presque les uns sur les autres. Le site K2 préserve des milliers de vestiges d’un lac préhistorique alimenté en crue qui agissait comme un piège osseux naturel il y a 72 millions d’années. Aux côtés de dinosaures locaux communs, les chercheurs ont découvert les premiers squelettes de titanosaures bien conservés jamais découverts dans la région. Le site révèle comment les anciens écosystèmes européens de dinosaures se sont formés et ont évolué au cours de cette période.
23/12/2025 sciencedaily ⚙ Traduction automatique
De nouveaux fossiles au Qatar révèlent une petite vache marine cachée depuis 21 millions d'années
os Qatar fossile
Des fossiles du Qatar ont révélé une petite espèce de vache marine nouvellement identifiée qui vivait dans le golfe Persique il y a plus de 20 millions d'années. Le site contient la collection la plus dense connue d’os fossiles de vaches marines, démontrant que ces animaux prospéraient autrefois dans de riches prairies d’herbiers marins. Leur rôle écologique reflète celui des dugongs modernes, qui remodèlent encore les fonds marins du Golfe en broutant. Les résultats pourraient aider les chercheurs à comprendre comment les écosystèmes d’herbiers marins réagissent aux changements environnementaux à long terme.
12/12/2025 sciencedaily ⚙ Traduction automatique
Cet os rare résout enfin le mystère du Nanotyrannus
os croissance musée fossile spécimen Nanotyrannus Tyrannosaurus découverte
Les scientifiques ont confirmé que Nanotyrannus était une espèce mature et non un jeune T. rex. Un examen microscopique de son os hyoïde a fourni la preuve clé, correspondant aux signaux de croissance observés dans les spécimens connus de T. rex. Cette découverte suggère un écosystème de tyrannosaures plus riche et plus compétitif qu’on ne le pensait auparavant. Il montre également comment les fossiles de musée et les analyses de pointe peuvent réécrire l’histoire préhistorique.
09/12/2025 sciencedaily ⚙ Traduction automatique
Des indices de boucherie révèlent que les Néandertaliens auraient pu avoir des « recettes familiales »
os chasse Israël
Les Néandertaliens vivant dans deux grottes voisines de l’ancien Israël préparaient leur nourriture de manières étonnamment différentes, selon de nouvelles preuves archéologiques. Bien qu’ils utilisaient les mêmes outils et chassaient les mêmes animaux, ils ont laissé derrière eux des motifs de coupures distincts sur les os, des indices de traditions culturelles transmises de génération en génération.
17/07/2025 sciencedaily-human-evo ⚙ Traduction automatique
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