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Partie anatomique

76 image(s) · 55 Actualités

Galerie d'images

Reconstructed skull of Duriavenator hesperis showing known material (white) of the holotype and only known specimen. Unknown bones based on related Eustreptospondylus oxoniensis. Scale bar is 10cm, image is 10px/cm. Cranial anatomy based on Benson (2008) "A redescription of "Megalosaurus" hesperis (Dinosauria, Theropoda) from the Inferior Oolite (Bajocian, Middle Jurassic) of Dorset, United Kingdom"
Taxons Duriavenator

Reconstructed skull of Duriavenator hesperis showing known material (white) of the holotype and only known specimen. Unknown bones based on related Eustreptospondylus oxoniensis. Scale bar is 10cm, image is 10px/cm. Cranial anatomy based on Benson (2008) "A redescription of "Megalosaurus" hesperis (Dinosauria, Theropoda) from the Inferior Oolite (Bajocian, Middle Jurassic) of Dorset, United Kingdom"

os écaille Royaume-Uni Bajocien +11
Representative bones of Pulanesaura eocollum. (a) anterior-to-middle cervical vertebrae (BP/1/6199) in left lateral view; (b) holotypic anterior-most dorsal neural arch (BP/1/6882) in left lateral and anterior views; (c) anterior dorsal neural arch (BP/1/6984) in anterior and right lateral views; (d) anterior mid-dorsal neural arch (BP/1/6183) in anterior and right lateral views; (e) middle dorsal neural arch (BP/1/6770) in posterior view; (f) anterior caudal vertebra (BP/1/6646) in right lateral and posterior views; (g) right humerus (BP/1/6193) in anterior view; (h) left ulna (BP/1/6210) in lateral and proximal views; (i) ?left clavicle (BP/1/6752) in dorsal view; (j) left pedal ungual I (BP/1/6186) in proximal and medial views; (k) left tibia (BP/1/6200) in anterior and lateral views; (l) right ischium (reversed) (BP/1/7366) in lateral view. Abbreviations: aidf, anterior infradiapophyseal fossa; ain, anterior incline of the neural spine; ep, epipophysis; hyp, hyposphene; mr, medial ridge; pp, parapophysis; prdl, prezygodiapophyseal lamina; prz, prezygapophyses; rf, radial fossa; spol, spinopostzygapophyseal lamina; vc, ventral convexity. Scale bars equal 5 cm in a-f and i, j; 10 cm in g, h, k, l. Silhouette drawn by BWM Photographs by BWM.
Taxons Pulanesaura

Representative bones of Pulanesaura eocollum. (a) anterior-to-middle cervical vertebrae (BP/1/6199) in left lateral view; (b) holotypic anterior-most dorsal neural arch (BP/1/6882) in left lateral and anterior views; (c) anterior dorsal neural arch (BP/1/6984) in anterior and right lateral views; (d) anterior mid-dorsal neural arch (BP/1/6183) in anterior and right lateral views; (e) middle dorsal neural arch (BP/1/6770) in posterior view; (f) anterior caudal vertebra (BP/1/6646) in right lateral and posterior views; (g) right humerus (BP/1/6193) in anterior view; (h) left ulna (BP/1/6210) in lateral and proximal views; (i) ?left clavicle (BP/1/6752) in dorsal view; (j) left pedal ungual I (BP/1/6186) in proximal and medial views; (k) left tibia (BP/1/6200) in anterior and lateral views; (l) right ischium (reversed) (BP/1/7366) in lateral view. Abbreviations: aidf, anterior infradiapophyseal fossa; ain, anterior incline of the neural spine; ep, epipophysis; hyp, hyposphene; mr, medial ridge; pp, parapophysis; prdl, prezygodiapophyseal lamina; prz, prezygapophyses; rf, radial fossa; spol, spinopostzygapophyseal lamina; vc, ventral convexity. Scale bars equal 5 cm in a-f and i, j; 10 cm in g, h, k, l. Silhouette drawn by BWM Photographs by BWM.

os humérus écaille vertèbre +1
PLATE X X X I ~ r.
The vertebral column of Anoplosaurus c~rto~ot~s.
Fig. l. Left lateral aspect of third to seventh cervical eentrums, showing how
the bodies of the vertebrae increase in depth from before backward,
and indicating at the upper anterior corner of each an attachment
for a cervical rib.
1 a. Visceral aspect of third (?) cervical vertebra, showing flattened and
rounded under surface, and expansion towards the anterior end.
Fig. 2. Left lateral aspect of fourteenth to eighteenth eentrums of the series,
showing the somewhat compressed appearance of upper parts of the
bodies of the last five dorsal vertebra.
2 a. Visceral aspect of the last dorsal vertebra, 1~o. 18.
2 b. Posterior (?) articular end of the same centrum, No. 18.
3. The sacrum, showing the neural or superior surface, and giving evi-
dence of the great expansion of the spinal cord in the region of the
second and third sacral vertebra. The outlets for the escape of the
sacral nerves at the sides of the centrum are best seen in the first
three vertebrae.
4. Dorsal surface of vertebral end of a sacral rib, showing the massive end
for attachment to the sides of the centrums of the second and third
vertebrm. Its worn upper surface gave attachment to the neural
arch.
5. Left lateral aspect of a sequence of six early caudal vertebrm numbered
25 to 30, showing decreasing depth of the centrum posteriorly, and
diminishing size in the surface for the attachment of the sacral rib
which remains in union with the 30th vertebra. The chevron facet, e,
also diminishes in size.
5 a. Posterior articular surface and facet for the chevron bone of the

vertebra ~No. 26.
Taxons Anoplosaurus

PLATE X X X I ~ r. The vertebral column of Anoplosaurus c~rto~ot~s. Fig. l. Left lateral aspect of third to seventh cervical eentrums, showing how the bodies of the vertebrae increase in depth from before backward, and indicating at the upper anterior corner of each an attachment for a cervical rib. 1 a. Visceral aspect of third (?) cervical vertebra, showing flattened and rounded under surface, and expansion towards the anterior end. Fig. 2. Left lateral aspect of fourteenth to eighteenth eentrums of the series, showing the somewhat compressed appearance of upper parts of the bodies of the last five dorsal vertebra. 2 a. Visceral aspect of the last dorsal vertebra, 1~o. 18. 2 b. Posterior (?) articular end of the same centrum, No. 18. 3. The sacrum, showing the neural or superior surface, and giving evi- dence of the great expansion of the spinal cord in the region of the second and third sacral vertebra. The outlets for the escape of the sacral nerves at the sides of the centrum are best seen in the first three vertebrae. 4. Dorsal surface of vertebral end of a sacral rib, showing the massive end for attachment to the sides of the centrums of the second and third vertebrm. Its worn upper surface gave attachment to the neural arch. 5. Left lateral aspect of a sequence of six early caudal vertebrm numbered 25 to 30, showing decreasing depth of the centrum posteriorly, and diminishing size in the surface for the attachment of the sacral rib which remains in union with the 30th vertebra. The chevron facet, e, also diminishes in size. 5 a. Posterior articular surface and facet for the chevron bone of the vertebra ~No. 26.

os vertèbre Anoplosaurus
Reconstructed skull of the holotype and only specimen of Leshansaurus qianweiensis based on the possibly related megalosaurid Dubreuillosaurus valesdunensis. Scale bar is 10cm, image is 10px/cm. Cranial anatomy from figures in Fei et al. (2009) "A new carnosaur from the Late Jurassic of Qianwei, Sichuan, China". White bones are figured, light grey bones are unfigured and minimally described.
Taxons Leshansaurus

Reconstructed skull of the holotype and only specimen of Leshansaurus qianweiensis based on the possibly related megalosaurid Dubreuillosaurus valesdunensis. Scale bar is 10cm, image is 10px/cm. Cranial anatomy from figures in Fei et al. (2009) "A new carnosaur from the Late Jurassic of Qianwei, Sichuan, China". White bones are figured, light grey bones are unfigured and minimally described.

os écaille Chine Jurassique +9
Skeletal diagram of Zuolong salleei, based on related basal coelurosaurs. Scale bar = 1 meter. Light colours indicate known material (white is known external bones, light grey is either palate, braincase, or sacrum). Dark colours indicate unknown material (partial bones or unknown braincase)
Taxons Zuolong

Skeletal diagram of Zuolong salleei, based on related basal coelurosaurs. Scale bar = 1 meter. Light colours indicate known material (white is known external bones, light grey is either palate, braincase, or sacrum). Dark colours indicate unknown material (partial bones or unknown braincase)

os écaille Coelurosauria Zuolong +1
Skeletal reconstruction of Laquintasaura venezuelae, a prionodontian ornithischian (after Barrett et al., 2014). A predentary was restored on the mandible of Laquintasaura, but there is no proof that this bone was present.
Taxons Laquintasaura

Skeletal reconstruction of Laquintasaura venezuelae, a prionodontian ornithischian (after Barrett et al., 2014). A predentary was restored on the mandible of Laquintasaura, but there is no proof that this bone was present.

os Laquintasaura Ornithischia Prionodontia
Preserved bones of Sanjuansaurus gordilloi (PVSJ 605), positioned as they were found in the field. Abbreviations: ca1–15, caudal vertebrae 1–15; c2–9, cervical vertebrae 2–9; d1–14, dorsal vertebrae 1–14; l Fe, left femur; l il, left ilium; l MII, left metatarsal II; l Sc, left scapula and coracoid; l Ti, left tibia; l Ul, left ulna; Ph, manual phalanx; R, rib; r As-Ca, right astragalus and calcaneum; r Fe, right femur; r Fi, right fibula; r Fe, right femur; r Mx, right maxilla; r Pu, right pubis; r Sc, right scapula and coracoid; r Ti, right tibia; s1–3, sacral vertebrae 1–3. Scale bars equals 20 cm.
Taxons Sanjuansaurus

Preserved bones of Sanjuansaurus gordilloi (PVSJ 605), positioned as they were found in the field. Abbreviations: ca1–15, caudal vertebrae 1–15; c2–9, cervical vertebrae 2–9; d1–14, dorsal vertebrae 1–14; l Fe, left femur; l il, left ilium; l MII, left metatarsal II; l Sc, left scapula and coracoid; l Ti, left tibia; l Ul, left ulna; Ph, manual phalanx; R, rib; r As-Ca, right astragalus and calcaneum; r Fe, right femur; r Fi, right fibula; r Fe, right femur; r Mx, right maxilla; r Pu, right pubis; r Sc, right scapula and coracoid; r Ti, right tibia; s1–3, sacral vertebrae 1–3. Scale bars equals 20 cm.

os écaille Sanjuansaurus
Holotype of Jakapil kaniukura (MPCA-PV-630), postcranial bones. Speculative silhouette showing preserved elements (a); osteoderm distribution is speculative and partial to show non-osteodermal elements); dorsal vertebra elements in dorsal (b), right lateral (c) and anterior (d,e) views; sacral vertebra in left lateral view (f); mid-caudal vertebra in left lateral view (g); fragment of the mid-shaft of a dorsal rib in posterior view (the enlarged, broken posterior edge is highlighted (h); expanded distal ends of two dorsal ribs (i); left scapula in lateral view (j); right scapula in lateral view (k); right coracoid in lateral view (l); left and right humeri in anterior view (m); probable right ulna in lateral view (n); metacarpals, non-ungual and ungual phalanx in dorsal views (o); left femur elements in anterior view (p); proximal end of the right fibula in lateral view (q); distal end of the left tibia in anterior view (r); ischial elements in side view (s); cervical osteoderms in dorsal view (t), flat scutes in dorsal view (u), spine-like osteoderm in side view (v) and ossicle in dorsal view (w). ac acromial crest, aco asymmetrical cervical osteoderm, alp anterolateral process, ap acromial process, at anterior trochanter, bb basal bone, ebr expanded broken rib edge, di diapophysis, dpc deltopectoral crest, ft fourth trochanter, gl glenoid, mc metacarpals, nc neural canal, ncs neurocentral suture, ph non-ungual phalanx, pp pubic peduncle, poz postzygapophyses, rug marginal rugosities, sb scapular blade, sc scute, tp transverse process, uph ungual phalanx.
Taxons Jakapil

Holotype of Jakapil kaniukura (MPCA-PV-630), postcranial bones. Speculative silhouette showing preserved elements (a); osteoderm distribution is speculative and partial to show non-osteodermal elements); dorsal vertebra elements in dorsal (b), right lateral (c) and anterior (d,e) views; sacral vertebra in left lateral view (f); mid-caudal vertebra in left lateral view (g); fragment of the mid-shaft of a dorsal rib in posterior view (the enlarged, broken posterior edge is highlighted (h); expanded distal ends of two dorsal ribs (i); left scapula in lateral view (j); right scapula in lateral view (k); right coracoid in lateral view (l); left and right humeri in anterior view (m); probable right ulna in lateral view (n); metacarpals, non-ungual and ungual phalanx in dorsal views (o); left femur elements in anterior view (p); proximal end of the right fibula in lateral view (q); distal end of the left tibia in anterior view (r); ischial elements in side view (s); cervical osteoderms in dorsal view (t), flat scutes in dorsal view (u), spine-like osteoderm in side view (v) and ossicle in dorsal view (w). ac acromial crest, aco asymmetrical cervical osteoderm, alp anterolateral process, ap acromial process, at anterior trochanter, bb basal bone, ebr expanded broken rib edge, di diapophysis, dpc deltopectoral crest, ft fourth trochanter, gl glenoid, mc metacarpals, nc neural canal, ncs neurocentral suture, ph non-ungual phalanx, pp pubic peduncle, poz postzygapophyses, rug marginal rugosities, sb scapular blade, sc scute, tp transverse process, uph ungual phalanx.

os crête vertèbre holotype +2
Caihong juji holotype specimen (PMoL-B00175). Photographs of the slab (a) and counter slab (b) and line drawing (c) of the specimen based on both slabs. Photograph (d) and line drawing (e) of a composite of the rostrum of the skull and mandible exposed on the counter slab and the post-rostrum cranium exposed on the slab. Arrows indicate lacrimal crests. Question mark indicates uncertain identification. Scale bars: 10 cm a–c, 1 cm d and e. aof antorbital fenestra, cav caudal vertebra, cev cervical vertebra, dr dorsal rib, dv dorsal vertebra, ect ectopterygoid, emf external mandibular fenestra, en external naris, f feather, fu furcula, ga gastralia, hy hyoid, il ilium, is ischium, la left angular, lar left articular, lc left coracoid, lcr lacrimal crest, ld left dentary, lf left, frontal, lfe left femur, lh left humerus, lj left jugal, ll left lacrimal, lma left maxilla, lm left manus, ln left nasal, lp left pes, lpa left palatine, lpo left postorbital, lq left quadrate, lqj left quadratojugal, lr left radius, ls left scapula, lsp left splenial, lsa left surangular, lsq left squamosal, lt left tibiotarsus, lu left ulna, ma mandible, mf maxillary fenestra, o orbit, p parietal, pm premaxilla, pt pterygoid, pu pubis, rar right articular, rc right coracoid, rd right dentary, rfe right femur, rh right humerus, rm right manus, rp right pes, rpra right prearticular, rq right quadrate, rr right radius, rs right scapula, rt right tibiotarsus, ru right ulna, scl sclerotic bones, sk skull, sy synsacrum
Taxons Caihong

Caihong juji holotype specimen (PMoL-B00175). Photographs of the slab (a) and counter slab (b) and line drawing (c) of the specimen based on both slabs. Photograph (d) and line drawing (e) of a composite of the rostrum of the skull and mandible exposed on the counter slab and the post-rostrum cranium exposed on the slab. Arrows indicate lacrimal crests. Question mark indicates uncertain identification. Scale bars: 10 cm a–c, 1 cm d and e. aof antorbital fenestra, cav caudal vertebra, cev cervical vertebra, dr dorsal rib, dv dorsal vertebra, ect ectopterygoid, emf external mandibular fenestra, en external naris, f feather, fu furcula, ga gastralia, hy hyoid, il ilium, is ischium, la left angular, lar left articular, lc left coracoid, lcr lacrimal crest, ld left dentary, lf left, frontal, lfe left femur, lh left humerus, lj left jugal, ll left lacrimal, lma left maxilla, lm left manus, ln left nasal, lp left pes, lpa left palatine, lpo left postorbital, lq left quadrate, lqj left quadratojugal, lr left radius, ls left scapula, lsp left splenial, lsa left surangular, lsq left squamosal, lt left tibiotarsus, lu left ulna, ma mandible, mf maxillary fenestra, o orbit, p parietal, pm premaxilla, pt pterygoid, pu pubis, rar right articular, rc right coracoid, rd right dentary, rfe right femur, rh right humerus, rm right manus, rp right pes, rpra right prearticular, rq right quadrate, rr right radius, rs right scapula, rt right tibiotarsus, ru right ulna, scl sclerotic bones, sk skull, sy synsacrum

os crête plume humérus +8
Partial skull and anterior cervical vertebrae of unidentified pliosaurid plesiosaurian (MPPL 18797) from the uppermost Callovian–middle Oxfordian of Kaberlaba (Asiago, Italy), in left lateral view. Photograph (A) and explanatory drawing (B). White, preserved bone surfaces; dark grey, preserved margins of skull fenestrae; light grey, eroded bone surface; cross hatching, broken bone.
Taxons Anguanax

Partial skull and anterior cervical vertebrae of unidentified pliosaurid plesiosaurian (MPPL 18797) from the uppermost Callovian–middle Oxfordian of Kaberlaba (Asiago, Italy), in left lateral view. Photograph (A) and explanatory drawing (B). White, preserved bone surfaces; dark grey, preserved margins of skull fenestrae; light grey, eroded bone surface; cross hatching, broken bone.

os dessin Italie Callovien +6
Identifier: annalsofmedicalh01pack (find matches)
Title: Annals of medical history
Year: 1917 (1910s)
Authors:  Packard, Francis R. (Francis Randolph), 1870-1950
Subjects:  Medicine
Publisher:  New York P.B. Hoeber
Contributing Library:  Gerstein - University of Toronto
Digitizing Sponsor:  University of Toronto

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Text Appearing Before Image:
ail strongly Hexed, and the toescontracted and appressed. The whole atti-tude strongly suggests a spastic distress,possibly brought on by some form ofpoisoning of the central nervous system,from infection or the deglutition of somepoisonous substance. 14. Osteomalacia is evidently the causeof the hypertrophy of the bones of Lim-nocyron potens, an early carnivore from theWashakie Eocene of Wyoming, nearly3,000,000 years old. MATERIALS AND METHODS The material described in the presentpaper has been loaned the writer lor de-scription by the Field Museum of Chii Osborn: Hull. Amcr. \lus. Natl. Hist., 1917,vol. 35. !>• 733. P>- 28. Studies in Paleopathology 393 by the American Museum of Natural His-tory of New York City, by Walker Museumof the University of Chicago, and by the Uni-versity of Kansas Natural History Museum. made by the well-known petrographic meth-ods so common in all geological labora-tories. The diagnoses, where they are at-tempted, arc made from comparisons of the
Text Appearing After Image:
Fig. 20. The skeleton of Strutbiomimus altus, a small dinosaur from the BeliyRiver series (Cretaceous), Red Deer River, Alberta, Canada, now regarded as ofapproximately the same age as the Judith River series. The unique feature ofthe skull is the total absence of teeth, with a size of skull one-third larger thanthe ostrich and a length of body of about fifteen feet. The position of the skeletonis decidedly that of the opisthotonos which may be regarded as an indication ofdisease. (After Osborn). A beautiful specimen of an osteoma, theonly one known so far, on the vertebra of aKansas Cretaceous mosasaur, was given thewriter by Dr. J. M. Armstrong of St. Paul.The writer expresses his obligations to thegentlemen connected with the above-men-tioned institutions and to Dr. Armstrong.The methods used are a combination ofprocedures in the various lines involved.Microscopic sections, which can be madethin enough for immersion lens study, are material with similar lesions in recent hu-man mat

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Taxons Hexing

Identifier: annalsofmedicalh01pack (find matches) Title: Annals of medical history Year: 1917 (1910s) Authors: Packard, Francis R. (Francis Randolph), 1870-1950 Subjects: Medicine Publisher: New York P.B. Hoeber Contributing Library: Gerstein - University of Toronto Digitizing Sponsor: University of Toronto 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: ail strongly Hexed, and the toescontracted and appressed. The whole atti-tude strongly suggests a spastic distress,possibly brought on by some form ofpoisoning of the central nervous system,from infection or the deglutition of somepoisonous substance. 14. Osteomalacia is evidently the causeof the hypertrophy of the bones of Lim-nocyron potens, an early carnivore from theWashakie Eocene of Wyoming, nearly3,000,000 years old. MATERIALS AND METHODS The material described in the presentpaper has been loaned the writer lor de-scription by the Field Museum of Chii Osborn: Hull. Amcr. \lus. Natl. Hist., 1917,vol. 35. !>• 733. P>- 28. Studies in Paleopathology 393 by the American Museum of Natural His-tory of New York City, by Walker Museumof the University of Chicago, and by the Uni-versity of Kansas Natural History Museum. made by the well-known petrographic meth-ods so common in all geological labora-tories. The diagnoses, where they are at-tempted, arc made from comparisons of the Text Appearing After Image: Fig. 20. The skeleton of Strutbiomimus altus, a small dinosaur from the BeliyRiver series (Cretaceous), Red Deer River, Alberta, Canada, now regarded as ofapproximately the same age as the Judith River series. The unique feature ofthe skull is the total absence of teeth, with a size of skull one-third larger thanthe ostrich and a length of body of about fifteen feet. The position of the skeletonis decidedly that of the opisthotonos which may be regarded as an indication ofdisease. (After Osborn). A beautiful specimen of an osteoma, theonly one known so far, on the vertebra of aKansas Cretaceous mosasaur, was given thewriter by Dr. J. M. Armstrong of St. Paul.The writer expresses his obligations to thegentlemen connected with the above-men-tioned institutions and to Dr. Armstrong.The methods used are a combination ofprocedures in the various lines involved.Microscopic sections, which can be madethin enough for immersion lens study, are material with similar lesions in recent hu-man mat 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 vertèbre livre musée +11
A diagram showing the bones and feathering preserved in IVPP V 12638, the holotype of Yixianosaurus longimanus, a feathered dinosaur.
Taxons Yixianosaurus

A diagram showing the bones and feathering preserved in IVPP V 12638, the holotype of Yixianosaurus longimanus, a feathered dinosaur.

os holotype Dinosauria Yixianosaurus
Outline and overview of the connected slabs TWE 480000454-A, -B, -D, -E, and -M.
TWE 480000454-A shows a single plate-like girdle bone (is). TWE 480000454-B contains
disarticulated vertebrae from the posterior presacral and sacral region (c1-11, na1-3),
fragments of dorsal ribs (dr1, dr2), elements of gastral ribs (unlabelled), the second ischium
(is), the round, plate-like pubis (pu), and three bones, most likely representing sacral- or
caudal ribs (?cr1-3). TWE 480000454-D, -E, and -M mainly contain dorsal ribs (dr3-9) and
elements of gastral ribs as well as two more isolated halves of neural arches (na4, na5), and a

caudal rib (cr1).
Taxons Pararcus

Outline and overview of the connected slabs TWE 480000454-A, -B, -D, -E, and -M. TWE 480000454-A shows a single plate-like girdle bone (is). TWE 480000454-B contains disarticulated vertebrae from the posterior presacral and sacral region (c1-11, na1-3), fragments of dorsal ribs (dr1, dr2), elements of gastral ribs (unlabelled), the second ischium (is), the round, plate-like pubis (pu), and three bones, most likely representing sacral- or caudal ribs (?cr1-3). TWE 480000454-D, -E, and -M mainly contain dorsal ribs (dr3-9) and elements of gastral ribs as well as two more isolated halves of neural arches (na4, na5), and a caudal rib (cr1).

os Pararcus
Fig. 5. Forelimb bones of the titanosaurian sauropod Bustingorrytitan shiva gen. et sp. nov. from “Bustingorry II” site, Neuquén Province, Argentina,
upper Cenomanian. A. Left coracoid (holotype, MMCH-Pv 59/13) in lateral view. B. Left scapula (holotype, MMCH-Pv 59/11) in lateral view. C. Left
humerus (holotype, MMCH-Pv 59/21) in proximal (C1), anterior (C2), and distal (C3) views. D. Right radius (holotype, MMCH-Pv 59/22) in posterior
view. E. Left sternal plate (holotype, MMCH-Pv 59/15) in dorsal view. F. Articulated metacarpals I–V (holotype, MMCH-Pv 59/25–29) in proximal
(F1), anterior (F2) and distal (F3) views. G. Right ulna (holotype, MMCH-Pv 59/23) in medial (G1) and proximal (G2) views. Abbreviations: cf, coracoid

foramen; gas, glenoid articular surface; igl, infraglenoid lip; I–V, metacarpals. Scale bars 200 mm.
Taxons Bustingorrytitan

Fig. 5. Forelimb bones of the titanosaurian sauropod Bustingorrytitan shiva gen. et sp. nov. from “Bustingorry II” site, Neuquén Province, Argentina, upper Cenomanian. A. Left coracoid (holotype, MMCH-Pv 59/13) in lateral view. B. Left scapula (holotype, MMCH-Pv 59/11) in lateral view. C. Left humerus (holotype, MMCH-Pv 59/21) in proximal (C1), anterior (C2), and distal (C3) views. D. Right radius (holotype, MMCH-Pv 59/22) in posterior view. E. Left sternal plate (holotype, MMCH-Pv 59/15) in dorsal view. F. Articulated metacarpals I–V (holotype, MMCH-Pv 59/25–29) in proximal (F1), anterior (F2) and distal (F3) views. G. Right ulna (holotype, MMCH-Pv 59/23) in medial (G1) and proximal (G2) views. Abbreviations: cf, coracoid foramen; gas, glenoid articular surface; igl, infraglenoid lip; I–V, metacarpals. Scale bars 200 mm.

os humérus écaille Argentine +4
Autapomorphies proposed for Diuqin lechiguanae gen. et sp. nov. (MUCPv 1401), with images generated from three-dimensional scans of selected bones. A–B, posteriormost (last) sacral neural arch (MUCPv 1401/1) in dorsal (A) and posterior (B) views. C, anterior caudal neural arch (MUCPv 1401/2) in dorsal view. D, left humerus (MUCPv 1401/4) in lateral view. Abbreviations: al, accessory lamina; dldpr, distolateral deltopectoral ridge; for, foramen. Scale bars equal 3 centimeters
Taxons Diuqin

Autapomorphies proposed for Diuqin lechiguanae gen. et sp. nov. (MUCPv 1401), with images generated from three-dimensional scans of selected bones. A–B, posteriormost (last) sacral neural arch (MUCPv 1401/1) in dorsal (A) and posterior (B) views. C, anterior caudal neural arch (MUCPv 1401/2) in dorsal view. D, left humerus (MUCPv 1401/4) in lateral view. Abbreviations: al, accessory lamina; dldpr, distolateral deltopectoral ridge; for, foramen. Scale bars equal 3 centimeters

os humérus écaille Diuqin +1
(A), silhouette of Maip macrothorax showing the preserved bones in white. (B), reconstruction of the thoracic cavity of Maip at level of D6. (C), interpretative drawing of the excavation of Maip showing the original disposition of the bones. Abbreviations: a, axis; c, coracoid; ind, indeterminate bone; g, gastralia; r, rib; v, vertebrae.
Taxons Maip

(A), silhouette of Maip macrothorax showing the preserved bones in white. (B), reconstruction of the thoracic cavity of Maip at level of D6. (C), interpretative drawing of the excavation of Maip showing the original disposition of the bones. Abbreviations: a, axis; c, coracoid; ind, indeterminate bone; g, gastralia; r, rib; v, vertebrae.

os dessin Maip fouille
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Actualités

Des dés en os anciens révèlent 12 000 ans d'histoire du jeu en Amérique
os jeu culture étude
Il y a plus de 12 000 ans, les chasseurs-cueilleurs amérindiens fabriquaient et utilisaient déjà des dés, des milliers d’années avant que des outils similaires n’apparaissent ailleurs. Ces « lots binaires » d’os agissaient comme des pièces de monnaie primitives, produisant des résultats aléatoires pour les jeux de hasard. Une nouvelle étude montre qu’il ne s’agissait pas d’objets accidentels mais d’outils soigneusement conçus et utilisés dans de nombreuses régions et cultures.
02/04/2026 sciencedaily-fossils ⚙ Traduction automatique
Les scientifiques ont trouvé un bébé dinosaure caché dans la roche et il est étonnamment mignon
os dessin Corée du Sud Dinosauria Doolysaurus tomographie découverte crâne
Des scientifiques ont découvert un bébé dinosaure rare en Corée du Sud et l'ont baptisé Doolysaurus, en hommage à un célèbre personnage de dessin animé. Grâce à des tomodensitogrammes de pointe, ils ont découvert des os cachés, notamment un crâne, dans la roche beaucoup plus rapidement que les méthodes traditionnelles. Le jeune dinosaure, peut-être duveteux et ressemblant à un agneau, avait même des calculs gastriques révélant qu'il mangeait un mélange de plantes et de petits animaux. Cette découverte suggère que de nombreux autres dinosaures pourraient encore être cachés dans les roches coréennes.
01/04/2026 sciencedaily ⚙ Traduction automatique
Certains dinosaures pouvaient s'élever comme des géants, jusqu'à devenir trop gros
os Dinosauria
Certains sauropodes plus petits pouvaient se tenir debout sur leurs pattes postérieures avec une facilité surprenante, leur donnant accès à une nourriture plus riche et un avantage défensif. Des simulations informatiques montrent que leurs os supportent mieux le stress que ceux de leurs parents plus grands. Cependant, à mesure qu’ils grandissaient, le poids rendait cette posture beaucoup plus difficile à maintenir. Ce qui a commencé comme une astuce utile dans la jeunesse est devenu une démarche stratégique plus limitée à l’âge adulte.
30/03/2026 sciencedaily ⚙ Traduction automatique
Il a fallu 40 ans au T. rex pour atteindre sa taille réelle, selon une étude
os croissance prédateur spécimen Tyrannosaurus étude
Le Tyrannosaurus rex a peut-être mis beaucoup plus de temps à grandir que les scientifiques ne le pensaient autrefois. En analysant les anneaux de croissance des os fossilisés des pattes de 17 spécimens de tyrannosaures et en utilisant de nouvelles méthodes statistiques, les chercheurs ont découvert que le célèbre prédateur avait probablement mis environ 40 ans pour atteindre sa taille maximale, soit environ huit tonnes, au lieu des 25 ans précédemment estimés.
05/03/2026 sciencedaily ⚙ Traduction automatique
L'ADN ancien résout le mystère vieux de 12 000 ans d'un trouble génétique rare de la croissance
os ADN croissance Italie découverte génétique
Un double enterrement de la période glaciaire en Italie a donné lieu à une révélation génétique étonnante. L'ADN d'une mère et d'une fille ayant vécu il y a plus de 12 000 ans montre que la plus jeune souffrait d'un trouble de croissance héréditaire rare, confirmé par des mutations dans un gène clé de la croissance osseuse. Sa mère portait une version plus douce de la même mutation. Cette découverte résout non seulement un mystère de longue date, mais prouve également que les maladies génétiques rares remontent loin dans la préhistoire.
17/02/2026 sciencedaily ⚙ Traduction automatique
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