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Figure 3 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 3. Holotype (MCT 1488-R), made up of cervical, dorsal, and sacral vertebrae, and the paratype (MCT 1719-R), made up of caudal vertebrae, of Trigonosaurus pricei. Scale bar: 20 cm.
Figure 13. A in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 13. A, angular variation of D2 over D3 in the still articulated fossil. B–G, angular variation of D2 over D3 in cartilaginous neutral postures with soft-tissue thickness as follows: B, 2.5%; C, 5%; D, 10%; E, 15%; F, 20%; G, 25%. H, detail of the dorsal vertebrae D2 and D3 (highlighted) directing the neck to an elevated height. I, axial skeleton set with a more vertical direction for the neck. No scale.
Figure 11 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 11. Caudal cartilaginous neutral posture: neutral pose of the caudal region of Trigonosaurus pricei with percentages of soft-tissue thickness as follows: A, 2.5%; B, 5%; C, 10%; D, 15%; E, 20%; F, 25%. In dark grey are shown reconstructed elements based on the morphology of MCT 1719-R vertebrae and close taxa. No scale.
Figure 12 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 12. Representation of the neutral pose with soft-tissue thickness combinations, in cervical, dorsal, and caudal order, respectively, as follows: A, 2.5%, 5%, 5%; B, 5%, 5%, 5%; C, 10%, 5%, 5%; D, 2.5%, 5%, 10%; E, 5%, 5%, 10%; F, 10%, 5%, 10%; G, 2.5%, 5%, 15%; H, 5%, 5%, 15%; I, 10%, 5%, 15%. The skeletons in each row share the same tail pose; in each column they share the same neck pose, and the trunk pose is constant. No scale.
Figure 6 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 6. Representation of the process of alignment and angulation of the vertebrae in the cartilaginous neutral posture. A, Cv9 and Cv10 cervical vertebrae were aligned based on the supposed horizontality of the neural canal. Arrow 1 indicates the place where the intervertebral soft tissue is located. B, the vertebrae are brought together and aligned, maintaining the distance corresponding to the thickness of the intervertebral soft-tissue. C, the anterior vertebra is displaced in relationship to the posterior one in the dorsal direction (ventral or lateral). Arrow 2 indicates where the centre of rotation is located. D, condyle similar to a paraboloid and the point where soft tissue was positioned. The apex of the paraboloid is a zero point and is furthest from the vertebral centrum. No scale.
Figure 10 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 10. Dorsal cartilaginous neutral posture: neutral pose of the dorsal region with percentages of soft-tissue thickness as follows: A, 2.5%; B, 5%; C, 10%; D, 15%; E, 15%; F, 25%. No scale.
Figure 1. A in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 1. A, lithostratigraphic map of the Bauru Basin showing the Bauru group. B, detailed lithostratigraphic map of the north-eastern Bauru Group deposits (from Soares et al. 2020a). C, Uberaba municipality, with the location of the BR050, Price 1, Price 6, and Ponte Alta (based on Silva Junior et al. 2022).
Figure 9 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 9. Cervical cartilaginous neutral posture: neutral pose of the cervical region of Trigonosaurus pricei with percentages of soft-tissue thickness as follows: A, 2.5%; B, 5%; C, 10%; D, 15%; E, 20%; F, 25%. Vertebrae were with non-articulated zygapophyses and vertebral centra were not displaced in any direction. In dark grey, the reconstructed elements are based on the morphology of the vertebrae of Trigonosaurus pricei and close taxa. No scale.
Figure 2 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 2. Comparison between the last sacral vertebrae of Baurutitan (MCT 1719-R) and Trigonosaurus (MCT 1488-R). A, last sacral vertebra (concave posterior facet), first biconvex, and anterior caudal vertebrae (Ca2 and Ca3) of Baurutitan. The red arrow indicates the opposite (biconvex) direction of the condyles in the vertebral centrum of the first caudal vertebra of Baurutitan. B, biconvex sacrum of Trigonosaurus. The thick red arrows indicate the first opisthocoelous sacral vertebra and the last procoelous sacral vertebra (convex posterior facet). C, E, articulation between MCT 1719-R and the sacrum MCT 1488-R. Red arrows highlight the direction of the neural spines in the last sacral and the first anterior caudal vertebrae. D, F, articulation between the caudal vertebrae of Baurutitan (MCT 1490-R; brown) and the sacrum MCT 1488-R. In E, the arrow indicates the more robust and posteriorly deflected feature of the transverse process of the anterior caudal vertebrae of MCT 1719-R, similar to the last sacral vertebra of MCT 1488-R.
Figure 4 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 4. Three-dimensional (3D) models of the reconstructed vertebrae (grey) and 3D models of the original vertebrae (brown), in dorsal view. The assemblage of cervical and dorsal vertebrae (Cv9–D10) belongs to the Trigonosaurus haplotype (MCT 1488-R). The assemblage of caudal vertebrae corresponds to the paratype of Trigonosaurus (MCT 1719-R). The red circles indicate the structures reconstructed through bilateral symmetry. The vertebrae Cv13–D1, D2–D3, D4–D5, D6–D7–D8, and D9–D10, connected by sediment (brown), were reconstructed in the zygapophyseal surface and the anterior and/or posterior portion of vertebral centra (grey). No scale.
Figure 5 in The axial biomechanics of Trigonosaurus pricei (Neosauropoda: Titanosauria) and the importance of the cervical-dorsal region to sauropod high-browser feeding strategy
Figure 5. Three-dimensional (3D) models of the reconstructed vertebrae (in grey) and 3D models of the original vertebrae (brown), in dorsal view. The assemblage of cervical and dorsal vertebrae (Cv9–D10) belongs to the Trigonosaurus haplotype (MCT 1488-R). The assemblage of caudal vertebrae corresponds to the paratype of Trigonosaurus (MCT 1719-R). The red circles indicate the structures reconstructed through bilateral symmetry. The vertebrae Cv13–D1, D2–D3, D4–D5, D6–D7–D8, and D9–D10, connected by sediment (brown), were reconstructed in the zygapophyseal surface and the anterior and/or posterior portion of vertebral centra (grey). No scale.
Combined Basal-bolus Insulin and Post-exercise Carbohydrate Feeding Strategy in T1DM
ClinicalTrials.gov study NCT02204839. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Time-restricted Feeding as a Dietary Strategy Against Metabolic Disturbances in Humans
ClinicalTrials.gov study NCT04351672. IPD Sharing: Not stated. Countries: 1. Publications: 1.
The Impact of Different Feeding Strategies During Packed Red Cell Transfusion on Intestinal Oxygenation
ClinicalTrials.gov study NCT02733718. IPD Sharing: UNDECIDED. Countries: 1. Publications: 4.
Comparison of Feeding Strategies for Hypoplastic Left Heart Syndrome Infants
ClinicalTrials.gov study NCT02657629. IPD Sharing: Not stated. Countries: 0. Publications: 6.
Arginine Feeding: a Novel Strategy to Improve Protein Metabolism in Cancer and the Response to Surgery
ClinicalTrials.gov study NCT00497380. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Bill disparity and feeding strategies amongst fossil and modern penguins
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Microplastics alter feeding strategies of a coral reef organism
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Data from: A unique feeding strategy of the extinct marine mammal Kolponomos: convergence on sabretooths and sea otters
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Data from: The response of bird feeding guilds to forest fragmentation reveals conservation strategies for a critically endangered African eco-region
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.