Explodable 3D Dog Skull for Veterinary Education
3D models of teeth and neurovascular system in the rostrum of Spinosauridae (theropod dinosaurs)
3D models of Ocnotherium skull
3D GM dataset of bird skeletal variation
Skeletal embryonic development in the catshark
Bony connexions of the petrosal bone of extant hippos
bony labyrinth (14) , inner ear (11) , Eocene (11) , geometric morphometrics (10) , CT-scan (10) , Oligocene (9) , Micro-CT (9)
Lionel Hautier (25) , Maëva Judith Orliac (24) , Laurent Marivaux (19) , Bastien Mennecart (16) , Renaud Lebrun (15) , Rodolphe Tabuce (15) , Pierre-Olivier Antoine (13)
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3D models related to the publication: Neurovascular system and dental renewal in the rostrum of Spinosauridae: new descriptions and implications on non-olfactive snout sensitivity of dinosaursFrederic Pittet
Published online: 24/06/2026 |
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M3#1755Right and left premaxillae of MNHN.F.GDF365 (mature specimen of Cristatusaurus lapparenti): bony surface, teeth and neurovascular system Type: "3D_surfaces"doi: 10.18563/m3.sf.1755 state:published |
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Spinosaurus maroccanus MNHN.F.SAM124 View specimen
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M3#1756Premaxillae and maxillae of MNHN.F.SAM124 (Spinosaurus maroccanus): bony surface, teeth and neurovascular system Type: "3D_surfaces"doi: 10.18563/m3.sf.1756 state:published |
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Cristatusaurus lapparenti MNHN.F.GDF366 View specimen
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M3#1757Right and left premaxillae of MNHN.F.GDF366 (young specimen of Cristatusaurus lapparenti): bony surface, teeth and neurovascular system Type: "3D_surfaces"doi: 10.18563/m3.sf.1757 state:published |
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M3#1758Right maxilla portion of MNHN.F.GDF366 (young specimen of Cristatusaurus lapparenti): bony surface, teeth and neurovascular system Type: "3D_surfaces"doi: 10.18563/m3.sf.1758 state:published |
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This 3D dataset contains the 3D models of the fossil specimens of Lilliputia gujjarorum, a new tiny dichobunoid artiodactyl from the early middle Eocene of northwestern India. The material includes the holotype, GU/RJ/003 (Rajouri Collection, H.N.B. Garhwal University), consisting of an associated left mandible fragment preserving the distal part of p4 and m1–3 (GU/RJ/003a) and a left maxillary fragment preserving P4 and M1–3 (GU/RJ/003b), as well as the referred specimen GU/RJ/005, a right mandible fragment preserving m1–2. The exceptionally small body size of Lilliputia, among the smallest known in Artiodactyla, together with its mosaic of primitive and derived dental characters, provides new insights into the early evolution, palaeobiogeography, and ecological diversification of artiodactyls during the Eocene.
Lilliputia gujjarorum GU/RJ/003a View specimen
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M3#1949left mandible fragment preserving the distal part of p4 and m1–3 Type: "3D_surfaces"doi: 10.18563/m3.sf.1949 state:in_press |
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Lilliputia gujjarorum GU/RJ/003b View specimen
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M3#1950left maxillary fragment preserving P4 and M1–3 Type: "3D_surfaces"doi: 10.18563/m3.sf.1950 state:in_press |
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Lilliputia gujjarorum GU/RJ/005 View specimen
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M3#1951right mandible fragment preserving m1–2 Type: "3D_surfaces"doi: 10.18563/m3.sf.1951 state:in_press |
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This contribution contains 3D models of upper molar rows of Cypriot mice (Mus cypriacus) and house mice (Mus musculus domesticus) from the island of Cyprus. Although morphologically similar and occasionally syntopic, the two species differ in habitat use and dietary strategies, ranging from anthropogenic resources in M. m. domesticus to a more natural and diversified trophic niche in M. cypriacus. Mandibular and molar shape variation was quantified through 3D geometric morphometrics, enabling the detection of interspecific differences, allometric trends, and age-related dental wear trajectories. The morphometric descriptors were evaluated for their capacity to capture phylogenetic divergence, ecological specialization, and ontogenetic dynamics. Results highlight that subtle morphological signals can expose fine-scale ecological processes and species-specific adaptive strategies.
Mus cypriacus APO1 View specimen
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M3#1897Upper molar row APO1 Mus cypriacus Type: "3D_surfaces"doi: 10.18563/m3.sf.1897 state:in_press |
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Mus cypriacus BET2 View specimen
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M3#1898Upper molar row BET2 Mus cypriacus Type: "3D_surfaces"doi: 10.18563/m3.sf.1898 state:in_press |
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Mus cypriacus FON1 View specimen
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M3#1899Upper molar row FON1 Mus cypriacus Type: "3D_surfaces"doi: 10.18563/m3.sf.1899 state:in_press |
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Mus cypriacus FON2 View specimen
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M3#1900Upper molar row FON2 Mus cypriacus Type: "3D_surfaces"doi: 10.18563/m3.sf.1900 state:in_press |
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Mus cypriacus KOU1 View specimen
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M3#1901Upper molar row KOU1 Mus cypriacus Type: "3D_surfaces"doi: 10.18563/m3.sf.1901 state:in_press |
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Mus musculus KOF1 View specimen
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M3#1902Upper molar row KOF1 Mus musculus domesticus Type: "3D_surfaces"doi: 10.18563/m3.sf.1902 state:in_press |
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Mus musculus LEF1 View specimen
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M3#1903Upper molar row LEF1 Mus musculus domesticus Type: "3D_surfaces"doi: 10.18563/m3.sf.1903 state:in_press |
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Mus musculus MEN1 View specimen
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M3#1904Upper molar row MEN1 Mus musculus domesticus Type: "3D_surfaces"doi: 10.18563/m3.sf.1904 state:in_press |
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Mus musculus TSE2 View specimen
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M3#1905Upper molar row TSE2 Mus musculus domesticus Type: "3D_surfaces"doi: 10.18563/m3.sf.1905 state:in_press |
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Mus musculus XYL5 View specimen
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M3#1906Upper molar row XYL5 Mus musculus domesticus Type: "3D_surfaces"doi: 10.18563/m3.sf.1906 state:in_press |
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The present 3D dataset contains the 3D models analyzed in Xing et al. (in press), Newly discovered Cretaceous dinosaur track sites from the Jiaguan Formation, Sichuan Province, China: ichnotaxonomy and preservation. The dataset includes photogrammetric 3D models of the specimens shown in Figures 6–9 and 16–17 of the original article. These correspond to track-bearing slabs and selected footprints from the Hongyangoukou and Jinyuxi tracksites and the Shimiaogou 2025 tracksite in the Gulin area, Sichuan Province, China. The Hongyangoukou material comprises three reddish-brown siltstone slabs preserving at least 61 theropod tracks, including nine trackways (HYGK-T1 to HYGK-T9) and isolated footprints (HYGK-TI1 onward). The Jinyuxi material comprises one isolated theropod natural cast (JYX-TI5) assigned to cf. Eubrontes, associated with microbially induced sedimentary structures (MISS). The Shimiaogou 2025 material comprises two slabs preserving at least 25 dinosaur footprints, including ornithopod trackways SMG25-O1 and SMG25-O2, theropod trackway SMG25-T1, and isolated footprints; all occur as natural positive reliefs. The 3D surface models are provided in PLY format.
Eubrontes isp. HYGK Slab 1 View specimen
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M3#1982All footprints in Fig. 6 are tridactyl theropod footprints assigned to Morphotype I and tentatively identified as Eubrontes-like. Fig. 6 (Hongyangoukou Slab 1) preserves at least 31 footprints, comprising seven trackways (HYGK-T1–T7) and 15 isolated footprints (HYGK-TI1–TI15). They are preserved as natural molds in reddish-brown siltstone and are heavily weathered, but they generally retain distinct tridactyl outlines and U- or V-shaped metatarsophalangeal regions. Claw impressions are present in some specimens (e.g., T3, T7-L1, and TI9), whereas digital pad impressions are absent. Footprint length ranges from 10.8 to 20.9 cm (mean ≈16.0 cm); the length-to-width ratio ranges from 1.1 to 1.7 (mean ≈1.4); mesaxony is weak (mean ≈0.47); and the divarication angle between digits II and IV ranges from 41° to 73° (mean ≈60°). The stride lengths of T1, T3, T4, and T6 are 144.5, 104.8, 122.3, and 64.5 cm, respectively, corresponding to 9.7, 5.6, 9.4, and 3.3 times their respective mean footprint lengths. T1 and T5 show outward rotations of about 4° and 9°, respectively. T3 is among the best-preserved examples, with digit III the longest and stoutest, digit IV the shortest, and clear claw impressions present on digits II and III, whereas TI10 is a complete tridactyl track. These footprints are therefore small theropod tracks of Morphotype I, tentatively assigned to Eubrontes-like. Type: "3D_surfaces"doi: 10.18563/m3.sf.1982 state:in_press |
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Eubrontes isp. HYGK Slab 2 View specimen
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M3#1983All footprints in Fig. 7 (Hongyangoukou Slab 2) are tridactyl theropod footprints assigned to Morphotype II and tentatively identified as Eubrontes-like. Slab 2 preserves at least 28 footprints, including two trackways (HYGK-T8 and HYGK-T9) and 18 isolated footprints (HYGK-TI16–TI33). Preservation is poorer than on Slab 1: impressions are shallower and more rounded overall; in T9 and in some isolated footprints (e.g., TI17, TI18, TI20, TI23, TI24, and TI26), discrete digit impressions are not recognizable and instead appear as oval depressions, whereas the remaining footprints show three discernible digit impressions. No digital pad impressions were observed; the metatarsophalangeal region is U-shaped, and relatively clear claw impressions are preserved in some tracks, such as T8-R1, TI18, and TI31. Footprint length ranges from 11.2 to 21.6 cm (mean 15.1 cm); the length-to-width ratio ranges from 0.9 to 1.7 (mean 1.4); mesaxony is weak (mean 0.45); and the divarication angle between digits II and IV ranges from 46° to 62° (mean 54°). The stride lengths of T8 and T9 are 60 cm and 116 cm, corresponding to approximately 4 and 7.7 times the average footprint length, respectively; the pace angulation of T9 is 166°. TI31 is relatively well preserved and markedly symmetrical, with digit III being the stoutest and longest, and with a distinct, sharp claw impression. Type: "3D_surfaces"doi: 10.18563/m3.sf.1983 state:in_press |
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Eubrontes isp. HYGK Slab 3 View specimen
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M3#1984All footprints in Fig. 8 (Hongyangoukou Slab 3) are tridactyl theropod footprints assigned to Morphotype I and tentatively identified as Eubrontes-like. Slab 3 preserves at least seven isolated footprints (HYGK-TI34–TI40) and no trackways; these footprints have relatively distinct tridactyl outlines and U- or V-shaped metatarsophalangeal regions, with some specimens (e.g., TI37 and TI38) preserving claw impressions but lacking digital pad impressions. The divarication angle between digits II and IV on Slab 3 ranges from 53° to 57° (mean 56°). As members of Morphotype I, they fall within the morphotype ranges for footprint length (10.8–20.9 cm; mean 16.0 cm), length-to-width ratio (1.1–1.7; mean 1.4), and mesaxony (weak; mean 0.47). Type: "3D_surfaces"doi: 10.18563/m3.sf.1984 state:in_press |
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Eubrontes isp. JYX-TI5 View specimen
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M3#1985JYX-TI5 is tentatively assigned to cf. Eubrontes. It is preserved as a natural cast on dark red quartz sandstone, with a preservation grade of 0.5–1.5. It shows largely complete digit impressions and a metatarsophalangeal region, as well as some claw impressions, but no digital pad impressions. The footprint has three distinct digit impressions, a relatively distinct U-shaped metatarsophalangeal region, a separation between the proximal region of digit III and the metatarsophalangeal region, and relatively clear claw impressions; its surface bears irregular linear ridges that likely represent microbially induced sedimentary structures (MISS). JYX-TI5 is 22.1 cm long, with a length-to-width ratio of 1.5, weak mesaxony (0.45), and a divarication angle between digits II and IV of 50°; the interdigital angle between digits II and III is slightly larger than that between digits III and IV. Type: "3D_surfaces"doi: 10.18563/m3.sf.1985 state:in_press |
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Grallator isp. SMG25 Slab 1 View specimen
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M3#1986Fig. 16 includes ornithopod footprints assigned to Caririchnium isp. and theropod footprints tentatively assigned to cf. Grallator. The ornithopod tracks are natural casts, clearest on Slab 1, and show a distinct quadripartite structure. Preservation grade is 1–2; footprint length is 23.5–31.2 cm (mean 27.3 cm), and length-to-width ratio is 1.2–1.5 (mean 1.4). They are highly symmetrical, with three clear rounded digit impressions and a sub-circular metatarsophalangeal region separated by a depression; claw impressions are absent, mesaxony is weak (0.24–0.38; mean 0.30), and the mean divarication angle between digits II and IV is 49°. The potential trackway SMG25-O2 has a pace length about 2.7 times the footprint length, a pace angulation of 111°, and inward rotation of about 15°. The theropod tracks are mostly isolated, with only one potential trackway, SMG25-T1, on Slab 1. Preservation grade is 1–2; footprints are small (8.5–20.4 cm) and generally slender, mostly complete tridactyl impressions with digit III longest and digit II shortest, V-shaped metatarsophalangeal regions, and faint claw impressions or digital pads in some tracks. SMG25-T1 comprises two footprints (mean length 19.9 cm, length-to-width ratio 1.9, mesaxony 0.54, mean divarication angle between digits II and IV 41°). Isolated footprint TI9 is the best preserved (length 9.8 cm, length-to-width ratio 2.1, mesaxony 0.72, divarication angle between digits II and IV 38°), with the metatarsophalangeal pad of digit IV aligned along the axis of digit III. Type: "3D_surfaces"doi: 10.18563/m3.sf.1986 state:in_press |
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Grallator isp. SMG25 Slab 2 View specimen
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M3#1987cf. Grallator is the dominant ichnotaxon in Fig. 17, which preserves 12 isolated cf. Grallator footprints, all preserved as natural positive reliefs with preservation grade 1–2. These small theropod tracks are 8.5–20.4 cm long and generally slender, and are mostly complete tridactyl impressions with digit III longest and digit II shortest, V-shaped metatarsophalangeal regions, and faint claw impressions or digital pads in some specimens. Type: "3D_surfaces"doi: 10.18563/m3.sf.1987 state:in_press |
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Veterinary education often relies on cadaveric specimens, but there is increasing demand for alternatives due to limited resources and ethical considerations. To address this, we developed a 3D printed ‘explodable’ model of a dog cranium with detachable, magnetized cranial components for teaching anatomy to students. This model was generated from a computed tomographic scan of a juvenile dog cranium for which cranial sutures were still partially open and segmented such that major cranial bones were isolated. All bones are printed at actual size and retain openings for cranial nerves and major vessels. This interactive model enhances anatomical education by supplying a hands-on tool that can be used either in the classroom setting or for independent learning and can be incorporated at the high school, college, or veterinary school level. It is currently being integrated into the first-year anatomy foundation course at Cornell University’s College of Veterinary Medicine. The model can be printed using any hobbyist or specialist 3D printer and we outline assembly instructions on how to attach magnets at prefabricated attachment points. Using both digital and 3D printed resources, we hope to help to address current shortages of anatomical resources and also inspire future generations of practicing veterinarians by making anatomy more accessible and engaging.
Canis lupus familiaris CUHL 9 View specimen
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M3#1858PLYs of the segmented cranial bones with pre-fabricated magnetic casings and shelves for assembly following 3D printing Type: "3D_surfaces"doi: 10.18563/m3.sf.1858 state:published |
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M3#1859PLYs of the segmented cranial bones of the "BOTTOM" cranial component. Downloadable for additional learning opportunities for students Type: "3D_surfaces"doi: 10.18563/m3.sf.1859 state:published |
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The present 3D Dataset contains 3D models (1 turtle and 7 mammals) from the french Lower Miocene described in: Gagnaison C., Mennecart B., Bailleul J., Barrier P., Chenot É., Toullec R., Potel S., Martin H., Millet A. & Memeteau D. 2023. — Nouvelles données géologiques et biostratigraphiques du gisement paléontologique à vertébrés de Mauvières, à Marcilly-sur-Maulne (Miocène inférieur et moyen ; Indre-et-Loire, France). Geodiversitas 45 (16): 449-478. https://doi.org/10.5252/geodiversitas2023v45a16.
Testudo promarginata ULB-MAUV-5 View specimen
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M3#1941Fragment of turtle shell of Testudo promarginata Type: "3D_surfaces"doi: 10.18563/m3.sf.1941 state:in_press |
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Plesiaceratherium sp. ULB-MAUV-20 View specimen
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M3#1942right metacarpus III of Plesiaceratherium sp. Type: "3D_surfaces"doi: 10.18563/m3.sf.1942 state:in_press |
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Brachyodus intermedius ULB-MAUV-21 View specimen
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M3#1943phalanx II of the lateral finger (III or IV) of Brachyodus intermedius (Mayet, 1908) Type: "3D_surfaces"doi: 10.18563/m3.sf.1943 state:in_press |
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Brachyodus intermedius ULB-MAUV-31 View specimen
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M3#1944cast of the right M3 of Brachyodus intermedius (Mayet, 1908) Type: "3D_surfaces"doi: 10.18563/m3.sf.1944 state:in_press |
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Ligeromeryx praestans ULB-MAUV-24 View specimen
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M3#1945right lower jaw bearing p3-m1 of Ligeromeryx praestans (Stehlin, 1937) Type: "3D_surfaces"doi: 10.18563/m3.sf.1945 state:in_press |
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Ligeromeryx praestans ULB-MAUV-25 View specimen
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M3#1946cast of the right antler of Ligeromeryx praestans (Stehlin, 1937) Type: "3D_surfaces"doi: 10.18563/m3.sf.1946 state:in_press |
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Megamphicyon carnutense ULB-MAUV-16 View specimen
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M3#1947right I1 of Megamphicyon carnutense (Antunes & Ginsburg, 1977) Type: "3D_surfaces"doi: 10.18563/m3.sf.1947 state:in_press |
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Hemicyon gargan ULB-MAUV-18 View specimen
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M3#1948cast of a left maxilla bearing M1-2 of Hemicyon gargan (Ginsburg & Morales, 1998) Type: "3D_surfaces"doi: 10.18563/m3.sf.1948 state:in_press |
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This contribution contains the 3D dataset analyzed in L. C. Gaetano, J. C. Sotomayor Chacón, M. R. Arcaria, N. Vega, J. M. Leardi, F. D. Seoane, and A. Otero. submitted. Earliest-diverging rhynchocephalian from Gondwana: a new sphenodontian from the Upper Triassic Los Colorados Formation (northwestern Argentina). Scientific Reports.
Coloradosphenodon lahni PULR-V264 View specimen
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M3#1855fragmentary skull and lower jaws Type: "3D_surfaces"doi: 10.18563/m3.sf.1855 state:in_press |
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The present 3D Dataset contains the 3D models produced for the paper "Szczygielski, T., Celestin, F., Adnet, S., Guinot, G., 2026. Triassic turtles of France: the first European Rhaetian stem turtle taxon (clades Testudinata, Proterochersidae). Swiss Journal of Palaeontology". The digitized material consists of shell and appendicular skeleton fragments of the first diagnostic stem turtle from the European Rhaetian and showcases a number of autapomorphic characters.
Bartassochersis lopezi UM-PDE2-01 View specimen
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M3#1907Left axillary region and base of the anterior plastral lobe (left hyoplastron, small medial fragment of the right hyoplastron, part of the posterior process of the entoplastron) Type: "3D_surfaces"doi: 10.18563/m3.sf.1907 state:in_press |
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Bartassochersis lopezi UM-PDE2-02 View specimen
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M3#1908Posterior plastral lobe Type: "3D_surfaces"doi: 10.18563/m3.sf.1908 state:in_press |
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Bartassochersis lopezi UM-PDE2-03 View specimen
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M3#1909First vertebral scute region, right side Type: "3D_surfaces"doi: 10.18563/m3.sf.1909 state:in_press |
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Bartassochersis lopezi UM-PDE2-04 View specimen
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M3#1910?Carapace fragment Type: "3D_surfaces"doi: 10.18563/m3.sf.1910 state:in_press |
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Bartassochersis lopezi UM-PDE2-05 View specimen
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M3#1911Left scapula Type: "3D_surfaces"doi: 10.18563/m3.sf.1911 state:in_press |
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Bartassochersis lopezi UM-PDE2-06 View specimen
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M3#1912Ungual Type: "3D_surfaces"doi: 10.18563/m3.sf.1912 state:in_press |
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Bartassochersis lopezi UM-PDE2-08 View specimen
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M3#1913Right hypoplastron Type: "3D_surfaces"doi: 10.18563/m3.sf.1913 state:in_press |
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Bartassochersis lopezi UM-PDE2-09 View specimen
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M3#1914Indeterminate Type: "3D_surfaces"doi: 10.18563/m3.sf.1914 state:in_press |
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Bartassochersis lopezi UM-PDE2-10 View specimen
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M3#1915?Mesoplastron/hypoplastron Type: "3D_surfaces"doi: 10.18563/m3.sf.1915 state:in_press |
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Bartassochersis lopezi UM-PDE2-11 View specimen
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M3#1916Left inguinal periphery (peripheral, hyoplastron) Type: "3D_surfaces"doi: 10.18563/m3.sf.1916 state:in_press |
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Bartassochersis lopezi UM-PDE2-12 View specimen
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M3#1917?Left side of a vertebral scute area with two partial pleural scute areas Type: "3D_surfaces"doi: 10.18563/m3.sf.1917 state:in_press |
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Bartassochersis lopezi UM-PDE2-13 View specimen
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M3#1918?Posterior pleural and supramarginal of marginal areas Type: "3D_surfaces"doi: 10.18563/m3.sf.1918 state:in_press |
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Bartassochersis lopezi UM-PDE2-14 View specimen
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M3#1919Posterior peripherals Type: "3D_surfaces"doi: 10.18563/m3.sf.1919 state:in_press |
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Bartassochersis lopezi UM-PDE2-15A View specimen
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M3#1920?Left edge of the anterior plastral lobe Type: "3D_surfaces"doi: 10.18563/m3.sf.1920 state:in_press |
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Bartassochersis lopezi UM-PDE2-15B View specimen
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M3#1921Indeterminate Type: "3D_surfaces"doi: 10.18563/m3.sf.1921 state:in_press |
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Bartassochersis lopezi UM-PDE2-16 View specimen
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M3#1922Indeterminate Type: "3D_surfaces"doi: 10.18563/m3.sf.1922 state:in_press |
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Bartassochersis lopezi UM-PDE2-17 View specimen
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M3#1923?Bridge fragment Type: "3D_surfaces"doi: 10.18563/m3.sf.1923 state:in_press |
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Bartassochersis lopezi UM-PDE2-19 View specimen
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M3#1924Right bridge region Type: "3D_surfaces"doi: 10.18563/m3.sf.1924 state:in_press |
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Bartassochersis lopezi UM-PDE2-20 View specimen
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M3#1925Left femoral bulge Type: "3D_surfaces"doi: 10.18563/m3.sf.1925 state:in_press |
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Bartassochersis lopezi UM-PDE2-21 View specimen
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M3#1926Indeterminate Type: "3D_surfaces"doi: 10.18563/m3.sf.1926 state:in_press |
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The present 3D Dataset contains a selection of 3D models analyzed in Billet G, Hautier L, Gaudin TJ, Flynn JJ, Ruf I, Carrillo JD, Ladevèze S, Lehmann T, Nicolas V, Orliac MJ, Tornero C, Wible JR, Wong N, Gaubert P. Submitted. Brain drain: Exceptional pattern of calvarial venation in pangolins and its phylogenetic significance for Ferae. Zoological Journal of the Linnean Society.
Phataginus tricuspis NHM-UK 48.13.26 View specimen
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M3#1847cranium & intradiploic canals (sinuses & diploic veins) Type: "3D_surfaces"doi: 10.18563/m3.sf.1847 state:published |
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Manis javanica NHM-UK 9.1.5.858 View specimen
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M3#1848cranium & intradiploic canals (sinuses & diploic veins) Type: "3D_surfaces"doi: 10.18563/m3.sf.1848 state:published |
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Felis silvestris UM-ZOOL-149N View specimen
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M3#1849cranium & intradiploic canals (sinuses & diploic veins) Type: "3D_surfaces"doi: 10.18563/m3.sf.1849 state:published |
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Erinaceus europaeus SMNS40759 View specimen
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M3#1850cranium & intradiploic canals (sinuses & diploic veins) Type: "3D_surfaces"doi: 10.18563/m3.sf.1850 state:published |
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Pterodon dasyuroides MNHN.F.Qu8301 View specimen
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M3#1851cranium & intradiploic canals (sinuses & diploic veins) Type: "3D_surfaces"doi: 10.18563/m3.sf.1851 state:published |
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This contribution contains the 3D models described and figured in the following publication: Paulina-Carabajal, A. and Nieto, M. N. In press. Brief comment on the brain and inner ear of Giganotosaurus carolinii (Dinosauria: Theropoda) based on CT scans. Ameghiniana. https://doi.org/10.5710/AMGH.25.10.2019.3237
Giganotosaurus carolinii MUCPv-CH-1 View specimen
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M3#504The current file contents 3D models of the braincase, brain, left and right inner ears Type: "3D_surfaces"doi: 10.18563/m3.sf.504 state:published |
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The present 3D Dataset contains the 3D models of the holotype and only specimen of Kalakocetus aurorae, a new cetacean retrieved from the Kalakot area in northwestern India. This specimen consists in a left hemimandible preserving the root of i3, p2, p4, m1 and m3 in situ. Its primitive morphology, with a tricuspid m3 morphologically intermediate between Raoellidae and Pakicetidae, makes it the first offshoot of Cetacea and provides crucial new elements to understand the setting up of the peculiar dental morphology of early cetaceans.
Kalakocetus aurorae GU/RJ/07 View specimen
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M3#1803left hemi mandible with p2, p4, m1, m3 Type: "3D_surfaces"doi: 10.18563/m3.sf.1803 state:published |
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M3#1804digitaly restored m1 Type: "3D_surfaces"doi: 10.18563/m3.sf.1804 state:published |
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M3#1805digital restoration of complete mandible Type: "3D_surfaces"doi: 10.18563/m3.sf.1805 state:published |
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M3#1810Scan Type: "3D_CT"doi: 10.18563/m3.sf.1810 state:published |
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The present dataset contains the 3D models of the cheek teeth of eight raccoons analyzed in Koomen, S. E., Lang, A. J. & Martin, T. (2026). Tooth Function of the Northern Raccoon (Procyon lotor) and Adaptations to Omnivory in the Order Carnivora. Journal of Morphology.
Procyon lotor ZFMK-MAM-2013.0341 View specimen
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M3#1838Cheek teeth of P. lotor specimen ZFMK-MAM-2013.0341 Type: "3D_surfaces"doi: 10.18563/m3.sf.1838 state:in_press |
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Procyon lotor ZFMK-MAM-1993.0289 View specimen
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M3#1839Cheek teeth of P. lotor specimen ZFMK-MAM-1993.0289 Type: "3D_surfaces"doi: 10.18563/m3.sf.1839 state:in_press |
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Procyon lotor ZFMK-MAM-2016.0912 View specimen
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M3#1840Cheek teeth of P. lotor specimen ZFMK-MAM-2016.0912 Type: "3D_surfaces"doi: 10.18563/m3.sf.1840 state:in_press |
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Procyon lotor ZFMK-MAM-2016.0914 View specimen
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M3#1841Cheek teeth of P. lotor specimen ZFMK-MAM-2016.0914 Type: "3D_surfaces"doi: 10.18563/m3.sf.1841 state:in_press |
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Procyon lotor ZFMK-MAM-2016.0923 View specimen
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M3#1842Cheek teeth of P. lotor specimen ZFMK-MAM-2016.0923 Type: "3D_surfaces"doi: 10.18563/m3.sf.1842 state:in_press |
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Procyon lotor ZFMK-MAM-2016.0937 View specimen
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M3#1843Cheek teeth of P. lotor specimen ZFMK-MAM-2016.0937 Type: "3D_surfaces"doi: 10.18563/m3.sf.1843 state:in_press |
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Procyon lotor ZFMK-MAM-2016.0938 View specimen
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M3#1844Cheek teeth of P. lotor specimen ZFMK-MAM-2016.0938 Type: "3D_surfaces"doi: 10.18563/m3.sf.1844 state:in_press |
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Procyon lotor ZFMK-MAM-2016.0967 View specimen
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M3#1845Cheek teeth of P. lotor specimen ZFMK-MAM-2016.0967 Type: "3D_surfaces"doi: 10.18563/m3.sf.1845 state:in_press |
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This contribution contains the 3D digital models of some fossil specimens of Wamradolops telloi Stutz and Pozodolops manuelorum Stutz (Metatheria: Polydolopimorphia), from several Palaeogene locations of Peruvian Amazonia. These taxa were described and analyzed in detail in the following publication: Stutz et al. (2026), Hidden diversity of Palaeogene metatherians: a new family of polydolopimorphian marsupials from Peruvian Amazonia. Zoological Journal of the Linnean Society. https://doi.org/10.1093/zoolinnean/zlag006.
Pozodolops manuelorum MUSM 4029 View specimen
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M3#1874Pozodolops manuelorum, fragmentary left dentary with p3–m1 Type: "3D_surfaces"doi: 10.18563/m3.sf.1874 state:published |
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Wamradolops telloi MUSM 4032 View specimen
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M3#1875Wamradolops telloi, fragmentary right dentary with m1–m2 Type: "3D_surfaces"doi: 10.18563/m3.sf.1875 state:published |
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Pozodolops manuelorum MUSM 4036 View specimen
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M3#1876Pozodolops manuelorum, holotype, fragmentary right maxilla with M1 Type: "3D_surfaces"doi: 10.18563/m3.sf.1876 state:published |
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Pozodolops manuelorum MUSM 4041 View specimen
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M3#1877Pozodolops manuelorum, fragmentary right dentary with m1 Type: "3D_surfaces"doi: 10.18563/m3.sf.1877 state:published |
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Pozodolops manuelorum MUSM 4058 View specimen
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M3#1878Pozodolops manuelorum, fragmentary left P3 Type: "3D_surfaces"doi: 10.18563/m3.sf.1878 state:published |
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Wamradolops telloi MUSM 4144 View specimen
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M3#1879Wamradolops telloi, fragmentary left dentary with p2–m1 Type: "3D_surfaces"doi: 10.18563/m3.sf.1879 state:published |
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Wamradolops telloi MUSM 4179 View specimen
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M3#1880Wamradolops telloi, holotype, partial skull, with right P2–M4 and left I4–M3, plus boneless lower teeth below upper teeth, belonging to the same individual Type: "3D_surfaces"doi: 10.18563/m3.sf.1880 state:published |
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Wamradolops telloi MUSM 4221 View specimen
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M3#1881Wamradolops telloi, fragmentary of right dentary with p3–m2 Type: "3D_surfaces"doi: 10.18563/m3.sf.1881 state:published |
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The democratization of 3D techniques in recent years provides exciting new opportunities for the study of complex fossils. In the present contribution, we provide a virtual reconstruction of a partial, disarticulated metriorhynchid (Metriorhynchidae, Thalattosuchia, Crocodylomorpha) skull from the Late Jurassic of northwestern Switzerland. This virtual reconstruction was used to produce high quality scientific illustrations of the whole skull for descriptive purposes. The reconstructed skull also served for the estimation of the total body length of the specimen and to propose a life reconstruction of the animal in its paleoenvironment. In an effort for transparency, we review the sources that were consulted for the life reconstruction and explain the choices that we had to make.
Torvoneustes jurensis BSY008-465 View specimen
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M3#1037Left dentary (3 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1037 state:published |
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M3#1038Right dentary (3 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1038 state:published |
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M3#1039Left ramus (2 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1039 state:published |
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M3#1040Right ramus (3 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1040 state:published |
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M3#1041Left splenial (2 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1041 state:published |
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M3#1042Right splenial (2 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1042 state:published |
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M3#1043Frontal and left prefrontal Type: "3D_surfaces"doi: 10.18563/m3.sf.1043 state:published |
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M3#1044Left maxilla (4 meshes) Type: "3D_surfaces"doi: 10.18563/m3.sf.1044 state:published |
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M3#1045Right maxilla Type: "3D_surfaces"doi: 10.18563/m3.sf.1045 state:published |
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M3#1046Left nasal Type: "3D_surfaces"doi: 10.18563/m3.sf.1046 state:published |
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M3#1047Right nasal Type: "3D_surfaces"doi: 10.18563/m3.sf.1047 state:published |
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M3#1048Parietal Type: "3D_surfaces"doi: 10.18563/m3.sf.1048 state:published |
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M3#1049Right postorbital Type: "3D_surfaces"doi: 10.18563/m3.sf.1049 state:published |
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M3#1050Right prefrontal Type: "3D_surfaces"doi: 10.18563/m3.sf.1050 state:published |
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M3#1051Right premaxilla Type: "3D_surfaces"doi: 10.18563/m3.sf.1051 state:published |
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M3#1052Left squamosal Type: "3D_surfaces"doi: 10.18563/m3.sf.1052 state:published |
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M3#1053Right squamosal Type: "3D_surfaces"doi: 10.18563/m3.sf.1053 state:published |
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M3#1054Reconstruction of the mandible Type: "3D_surfaces"doi: 10.18563/m3.sf.1054 state:published |
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M3#1055Reconstruction of the cranium Type: "3D_surfaces"doi: 10.18563/m3.sf.1055 state:published |
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We provide a 3D reconstruction of the skull of Latimeria chalumnae that can be easily accessed and visualized for a better understanding of its cranial anatomy. Different skeletal elements are saved as separate PLY files that can be combined to visualize the entire skull or isolated to virtually dissect the skull. We included some guidelines for a fast and easy visualization of the 3D skull.
Latimeria chalumnae MHNG 1080.070 View specimen
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M3#1254the skeletal elements of the skull of Latimeria chalumnae included in 26 different PLY files Type: "3D_surfaces"doi: 10.18563/m3.sf.1254 state:published |
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Macroevolution is integral to understanding the patterns of the diversification of life. As the life sciences increasingly use big data approaches, large multivariate datasets are required to test fundamental macroevolutionary hypotheses. In vertebrate evolution, large datasets have been created to quantify morphological variation, largely focusing on particular areas of the skeleton. We provide a landmarking protocol to quantify morphological variation in skeletal elements across the head, trunk, hindlimb and forelimb using 3-dimensional landmarks and semilandmarks, and present a large pan-skeletal database of bird morphology for 149 taxa across avian phylogeny using CT scan data. This large collection of 3D models and geometric morphometric data is open access and can be used in the future for new research, teaching and outreach. The 3D models and CT scans of the 149 specimens related to this project can be downloaded at MorphoSource (https://www.morphosource.org/projects/00000C420)
Menura novaehollandiae FMNH 336751 View specimen
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M3#5613D model of the left carpometacarpus of the superb lyrebird, Menura novaehollandia (displayed as a mirror image in the 3DHOP viewer). Type: "3D_surfaces"doi: 10.18563/m3.sf.561 state:published |
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M3#5623D model of the mandible of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.562 state:published |
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M3#5633D model of the right coracoid of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.563 state:published |
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M3#5643D model of the right scapula of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.564 state:published |
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M3#5653D model of the right tarsometatarsus of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.565 state:published |
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M3#5663D model of the sternum of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.566 state:published |
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M3#5673D model of the left femur of the superb lyrebird, Menura novaehollandiae (displayed as a mirror image in the 3DHOP viewer). Type: "3D_surfaces"doi: 10.18563/m3.sf.567 state:published |
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M3#5683D model of the skull of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.568 state:published |
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M3#5693D model of the left humerus of the superb lyrebird, Menura novaehollandiae (displayed as a mirror image in the 3DHOP viewer). Type: "3D_surfaces"doi: 10.18563/m3.sf.569 state:published |
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M3#5703D model of the synsacrum of the superb lyrebird, Menura novaehollandiae. Type: "3D_surfaces"doi: 10.18563/m3.sf.570 state:published |
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M3#5713D model of the left radius of the superb lyrebird, Menura novaehollandiae (displayed as a mirror image in the 3DHOP viewer). Type: "3D_surfaces"doi: 10.18563/m3.sf.571 state:published |
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M3#5723D model of the left tibiotarsus of the superb lyrebird, Menura novaehollandiae (displayed as a mirror image in the 3DHOP viewer). Type: "3D_surfaces"doi: 10.18563/m3.sf.572 state:published |
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M3#5733D model of the left ulna of the superb lyrebird, Menura novaehollandiae (displayed as a mirror image in the 3DHOP viewer). Type: "3D_surfaces"doi: 10.18563/m3.sf.573 state:published |
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The study of titanosaur paleobiology has been severely hampered by the incomplete nature of their fossil record, particularly the scarcity of well-preserved and relatively complete cranial remains. Even the most complete titanosaur skulls are often fractured, incomplete, or deformed, which has resulted in a limited knowledge of the paleobiology related to cranial anatomy, especially functional morphology. In this context, we present the digital restoration of the skull of the Argentinean titanosaur Sarmientosaurus musacchioi, created using the open-source 3D modeling software Blender. The digitally restored model is freely accessible to other researchers, facilitating broader research and comparative studies.
Sarmientosaurus mussacchioi MDT-PV 02 View specimen
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M3#1594Cranium and mandible of Sarmientosaurus mussacchioi Type: "3D_surfaces"doi: 10.18563/m3.sf.1594 state:published |
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M3#1599Original object provided by Gabriel Casal (cranium) Type: "3D_surfaces"doi: 10.18563/m3.sf.1599 state:published |
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This contribution contains the 3D model(s) described and figured in the following publication: Da Cunha, L., Fabre, P.-H. & Hautier, L. (2024) Springhares, flying and flightless scaly-tailed squirrels (Anomaluromorpha, Rodentia) are the squirrely mouse: comparative anatomy of the masticatory musculature and its implications on the evolution of hystricomorphy in rodents. Journal of Anatomy, 244, 900–928.
Anomalurus derbianus 21804 View specimen
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M3#1493Masticatory apparatus of Anomalurus Type: "3D_surfaces"doi: 10.18563/m3.sf.1493 state:published |
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Idiurus macrotis 29335 View specimen
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M3#1492Masticatory apparatus of Idiurus Type: "3D_surfaces"doi: 10.18563/m3.sf.1492 state:published |
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Zenkerella insignis 5.5.23.27 View specimen
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M3#1490Masticatory apparatus of Zenkerella Type: "3D_surfaces"doi: 10.18563/m3.sf.1490 state:published |
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Pedetes capensis NA View specimen
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M3#1491Masticatory apparatus of Pedetes Type: "3D_surfaces"doi: 10.18563/m3.sf.1491 state:published |
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The present Dataset contains the micro-CT scan of the head of an anonymous 54 year old female donor, at a voxel resolution of 145µm. The skin of the face has been masked in order to avoid the donor to be recognized.
Homo sapiens UM_HS_2018_09_13 View specimen
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M3#1152Micro-ct data set Type: "3D_CT"doi: 10.18563/m3.sf.1152 state:published |
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The present 3D Dataset contains the 3D models of Protocetus atavus described and figured in the following publication: Berger et al. (2025) The endocranial anatomy of Protocetids and its implications for early whale evolution.
Protocetus atavus SMNS-P-11084 View specimen
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M3#1654Textured model of the whole skull Type: "3D_surfaces"doi: 10.18563/m3.sf.1654 state:published |
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M3#1655Brain endocast Type: "3D_surfaces"doi: 10.18563/m3.sf.1655 state:published |
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