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22 results for “Triceratops”
FIG. 3 in The skull of Triceratops in the palaeontology gallery, Muséum national d'Histoire naturelle, Paris
FIG. 3. — Triceratops horridus Marsh, 1889; Upper Cretaceous, Lance Creek, Converse County, Wyoming, USA; skull MNHN 1912.20 in left lateral view. Abbreviations: Antf, antorbital fenestra; E, epoccipital; ExN, external nares; F, frontal; J, jugal; L, lachrymal; Ltf, lower temporal fenestra; Mx, maxilla; N, nasal; Nf, narial fossa; Nh, nasal horn; P, parietal; Pd, predentary; Pmx, premaxilla; Po, postorbital; Prf, prefrontal; Q, quadrate; Qj, quadratojugal; R, rostral; Sq, squamosal. Scale bar: 50 cm.
FIG. 2 in The skull of Triceratops in the palaeontology gallery, Muséum national d'Histoire naturelle, Paris
FIG. 2. — Triceratops horridus Marsh, 1889; Upper Cretaceous, Lance Creek, Converse County, Wyoming, USA; skull and predentary MNHN 1912.20, measurements in cm.
FIG. 1 in The skull of Triceratops in the palaeontology gallery, Muséum national d'Histoire naturelle, Paris
FIG. 1. — Triceratops horridus Marsh, 1889 (MNHN 1912.20), previously referred to as Triceratops calicornis Marsh, 1898; Upper Cretaceous, Lance Creek, Converse County, Wyoming, USA; skull and predentary in right anterolateral view.
FIG. 5 in The skull of Triceratops in the palaeontology gallery, Muséum national d'Histoire naturelle, Paris
FIG. 5. — Triceratops horridus Marsh, 1889; Upper Cretaceous, Lance Creek, Converse County, Wyoming, USA; braincase and right quadrate in posterior view (MNHN 1912.20). Abbreviations: Bo, basioccipital; Cn, cranial nerve; Co, occipital condyle; Eo, exoccipital; Fm, foramen magnum; J, jugal; Ls, laterosphenoid; Mx, maxilla; Q, quadrate; Qj, quadratojugal. Scale bar: 10 cm.
Tyrannosaurus Rex / Triceratops [SmithsonianDPO]
Repost of a 3D model courtesy of the Smithsonian's Digitization Program Office For more models and information about this model and their work visit them on the web at 3d.si.edu Direct link to the originl data set: https://3d.si.edu/t-rex > This T. rex skeleton was unearthed in Montana beginning in 1988. It is posed over a Triceratops horridus. While the T. rex is the fossilized remains of a single animal, the Triceratops is a composite model made possible through digital technology, scaling bones from different specimens to the same size to create this skeleton. ~ https://3d.si.edu/t-rex Source: Objaverse 1.0 / Sketchfab
Triceratops horridus - Retopologized
Original 3d scan by shadows44: https://sketchfab.com/models/53a4a2a8f62c4e5685e18f3033b5983a Source: Objaverse 1.0 / Sketchfab
Triceratops Ribs
Exposed Triceratops ribs from a trip to Montana with [PaleoProspectors](https://paleoprospectors.com/). My good friend Drew and I will be prepping what we found, and I will be scanning and uploading the finished results, so keep an eye out for that. Source: Objaverse 1.0 / Sketchfab
Triceratops Horridus Marsh
Smithsonian source data can be found [here](https://ids.si.edu/ids/media_view?id=3d_package:d8c623be-4ebc-11ea-b77f-2e728ce88125) This media file is in the public domain (free of copyright restrictions). You can copy, modify, and distribute this work without contacting the Smithsonian. For more information and to review the 3D disclaimer, visit the Smithsonian's [Terms of Use](https://www.si.edu/Termsofuse) page. Triceratops horridus Marsh, 1889 Common name: Dinosaur Taxonomy: Animalia Chordata Vertebrata Sauropsida Reptilia Archosauria Dinosauria Ornithischia Ceratopsia Ceratopsidae Published Name: Triceratops horridus Marsh, 1889 USNM Number: PAL500000 Data Source: NMNH - Paleobiology Dept. EDAN-URL: edanmdm:nmnhpaleobiology_3572783 Source: Objaverse 1.0 / Sketchfab
Supplementary photographs from: The Canadian fossil record supports anagenesis in Triceratops (Ornithischia, Ceratopsia)
Open the record for dataset details and reuse information.
Fig. 10 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 10. Cornutipo tricornis (Evans, 1934) (SAM). A–B, ♀ paratype. A, lateral habitus. B, dorsal habitus. C–D, ♀ paratype. C, lateral habitus. D, dorsal habitus. E, ♂ paratype, ventral habitus. F, nymph, dorsal habitus. © B. Parslow (SAM).
Fig. 4 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 4. Cornutipo chillagoensis sp. nov. ♀, paratype (QM). A, dorsal head and pronotum. B, ventral head and pronotum. C, lateral head and pronotum. D, ventral abdomen and terminalia. E, hind wing.
Fig. 5 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 5. Cornutipo chillagoensis sp. nov. ♂, holotype. A, lateral genitalia. B, posterolateral genitalia. C, posterior genitalia. D, subgenital plates and parameres, dorsal view. E, subgenital plates and parameres, ventral view. F, subgenital plates and parameres, dorsolateral view. G, subgenital plates and parameres, posterior view. H, aedeagus, left lateral view. I, aedeagus, right lateral view. J, aedeagus, right posterolateral view. K, aedeagus, posterior view. L, aedeagus, anterior view.
Fig. 6 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 6. Cornutipo chillagoensis sp. nov., in nature in Queensland, Chillagoe, 7 May 2022. A, specimen on stem of Acacia auriculiformis. B, specimen tended by Iridomyrmex sp. C, specimens tended by Papyrius nitidus. D, habitat, general view. E, typical A. auriculiformis shrub hosting C. chillagoensis sp. nov.
Fig. 3 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 3. Cornutipo chillagoensis sp. nov. ♀, paratype (QM). A, dorsal habitus. B, ventral habitus. C, lateral habitus. D, dorsolateral habitus.
Fig. 9 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 9. Cornutipo tricornis (Evans, 1934) (SAM). A, ♂ holotype, dorsal habitus. B, ♂ holotype, lateral habitus. C, ♂ holotype, left tegmen. D, ♂ holotype, aedeagus. E, ♂ holotype, parameres and subgenital plates. F, type series. G, labels. © B. Parslow (SAM).
Fig. 2 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 2. Cornutipo chillagoensis sp. nov. ♂, paratype (QM). A, dorsal head and pronotum. B, ventral head and pronotum. C, lateral head and pronotum. D, anterodorsal head and pronotum. E, ventral abdomen and terminalia.
Fig. 1 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 1. Cornutipo chillagoensis sp. nov. ♂ (QM). A, paratype, dorsal habitus. B, paratype, ventral habitus. C, paratype, lateral habitus. D, holotype, hind wing. E, paratype, dorsolateral habitus.
Fig. 7 in The "Triceratops" leafhoppers. A new species of the genus Cornutipo Evans, 1934 from Northern Queensland, Australia. (Hemiptera: Cicadellidae: Eurymelinae: Ipoini)
Fig. 7. Ant species tending Cornutipo chillagoensis sp. nov. A–B, Papyrius nitidus. A, lateral habitus. B, face. C–D, Iridomyrmex sp. C, lateral habitus. D, face.
Triceratops created in SculptrVR
Source: Objaverse 1.0 / Sketchfab
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia. in Bite-force estimation for Tyrannosaurus rex from tooth-marked bones
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia.
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