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FIGURE 3 in Soft-tissue anatomy of the Plesiosaur pectoral girdle inferred from basal Eosauropterygia taxa and the extant phylogenetic bracket
FIGURE 3. Muscle reconstruction of the pectoral girdle musculature of the Eosauropterygia using data from the extant phylogenetic bracket, the fossil record and developmental patterns.
FIGURE 5. M. subcoracoscapularis. Reconstruction for Neusticosaurus 1 in Soft-tissue anatomy of the Plesiosaur pectoral girdle inferred from basal Eosauropterygia taxa and the extant phylogenetic bracket
FIGURE 5. M. subcoracoscapularis. Reconstruction for Neusticosaurus 1 in anterior view, 2 in ventral view, 3 in lateral view, 4 in fleshed-out muscle reconstruction and 5 complete skeletal reconstruction in lateral view. Reconstruction for Ceresiosaurus 6 in anterior view, 7 in ventral view, 8 in lateral view, 9 fleshed-out muscle reconstruction and 10 complete skeletal reconstruction in lateral view. Reconstruction for Rhomaleosaurus 11 in anterior view, 12 in ventral view, 13 in lateral view, 14 fleshed-out muscle reconstruction and 15 complete skeletal reconstruction in lateral view.
Fig. 4. Soft tissue reconstructions. A in Petrosal bones of placental mammals from the Late Cretaceous of Uzbekistan
Fig. 4. Soft tissue reconstructions. A. Tympanic view of "Zhelestidae". B. Squamosal view of "Zhelestidae". C. Tympanic view of Prokennalestes (modified from Wible et al. 2001). D. Squamosal view of Prokennalestes (modified from Wible et al. 2001). E. Tympanic view of Didelphis virginiana (modified from Wible 1990). F. Squamosal view of Didelphis virginiana (modified from Wible 1990). G. Tympanic view of Kulbeckia kulbecke. H. Squamosal view of Kulbeckia kulbecke. Anterior towards the top in A, C, E, and G. Anterior towards the right in B, D, F, and H.
Maximized response by structural optimization of soft elastic composite systems
<p>This dataset contains the underlying data and numerical optimization codes for the paper</p> <p><em>L. Fischer and Andreas M. Menzel</em><br>Maximized response by structural optimization of soft elastic composite systems<br>PNAS Nexus <strong>3</strong>, <span>pgae353 </span>(2024) (DOI: <a href="https://doi.org/10.1093/pnasnexus/pgae353" target="_blank" rel="noopener">10.1093/pnasnexus/pgae353</a>).</p> <p>For more information, please see the included "Readme.txt" in the dataset "Zenodo.zip".</p>
Fig. 5 in Soft-tissue attachments in orthocerid and bactritid cephalopods from the Early and Middle Devonian of Germany and Morocco
Fig. 5. SEM micrographs of Bactrites, and Cycloceras of early Emsian age (Early Devonian) from Ouidane Chebbi (Tafilalt, Morocco). The specimens coated with carbon. A. Bactrites sp. C; PIMUZ 7272; A1, detail of the annular elevation; note the rugged surface of the adoral part as well as the right and the median lobe of the annular elevation; A2, dorsal view of the same, showing last formed septum and posterior portion of body chamber; note the tracking bands, the mural band, and the annular elevation. B. Cycloceras sp.; PIMUZ 7263; B1, lateral view of a part of the phragmocone; B2, B3, same specimen, details of the wrinkle layer; note that the wrinkles are asymmetric in cross section with the steeper slope pointing adapically. C. Cycloceras sp.; PIMUZ 7261; detail of the conchal furrow. D.?Bactrites sp.; PIMUZ 7269; D1, detail of the wrinkle layer; D2, same specimen detail of the wrinkle layer in a smaller scale, note the asymmetry; D3, same specimen, overview of the adoral part of the body chamber.
Fig. 2 in Soft-tissue attachments in orthocerid and bactritid cephalopods from the Early and Middle Devonian of Germany and Morocco
Fig. 2. Schematic outlines of the variability of the dorsal furrow in Acanthomichelinoceras commutatum (Giebel, 1852), showing the base of a chamber mould, with annular elevation dotted. Note the differences of the starting point of the dorsal furrow, sometimes within the mural area, sometimes within the annular elevation. A. NHW 56.9.05/402. B. NHW 56.9.05/404. C. MB.C.5366.4. D. MB.C.5366.1. Not to scale.
Fig. 1 in Soft-tissue attachments in orthocerid and bactritid cephalopods from the Early and Middle Devonian of Germany and Morocco
Fig. 1. Soft−tissue attachment structures in cephalopods from the Wissenbach Schiefer (early Eifelian). A. Bactrites gracile (Blumenbach, 1803), NHW 62.11/W−23/64, dorsal view, note the two different grayish bands (arrows) forming a lobe. B. Bactrites sp. A, NHW 402, dorsal view (B1), note two successive, slightly undulated grooves. Same specimen, lateral view (B). Same specimen, ventral view (B), note the small lobe in suture line. Same specimen, +
Figure 11 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 11. - The asymmetric liver of an angler, Lophius piscatorius, dorsal view. l.h.l.: left hepatic lobe; r.h.l.: right hepatic lobe. The black arrow indicates the anterior part of the specimen. Scale = 50 mm.
Figure 12 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 12. - Schematic distribution of the supramedulary neurons among teleostean fishes [modified from Mola and Cuoghi (2004)]. A: Type I present in Salmonidae, Syngnathidae, Cottidae, Labridae, Percidae and some Pleuronectiformes; B: Type II present in Lophiiformes, Tetraodontiformes and Batrachoidiformes. Legend: 1: spinal cord; 2: central canal; 3: supramedulary neurons. The black arrow indicates the anterior part of the spinal cord.
Figure 10 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 10. - The central nervous system of an angler (SL = 28.8 cm), Lophius piscatorius, dorsal view. cr.n.: cranial nerves; e.: encephalon; f.t.: filum terminale; op.n.: optic nerves; s.c.: spinal cord. The black arrow indicates the anterior part of the specimen. Scale = 50 mm.
Figure 7 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 7. - The thyroid gland of an angler, Lophius piscatorius, right lateral view. ly.v: lymphatic vessels; th.a: thyroidian artery; th.s: thyroidian sinus. The black arrow indicates the anterior part of the specimen. Scale = 3 mm.
Figure 8 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 8. - Horizontal section in the thyroid gland of an ocean sunfish, Mola mola, ventral view. c.b.v: cut blood vessels; th.t: thyroidian tissue. The black arrow indicates the anterior part of the specimen. Scale = 30 mm.
Figure 9 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 9. - Parasagittal section on a frozen specimen of a black seabream, Spondyliosoma cantharus, left lateral view. k: kidney; ov: ovary; sb: swimbladder; s.c: spinal cord. The black arrow indicates the anterior part of the specimen. Scale = 20 mm.
Figure 6 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 6. - Sagittal section of a frozen of a black seabream, Spondyliosoma cantharus, left lateral view. b.cav: buccal cavity; e: encephalon; s.c: spinal cord; th.i: thyroidian islets; v: ventricle. The black arrow indicates the anterior part of the specimen. Scale = 10 mm.
Figure 5 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 5. - Visceral anatomy of a Buntal puffer, Tetraodon palembangensis, ventral view. The swimbladder and the digestive tract have been put away. ab.cav: abdominal cavity; c.oe: cut oesophagus; c.pc: cut pericardium; k: kidneys; v: ventricle. The black arrow indicates the anterior part of the specimen. Scale = 10 mm.
Figure 4 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 4. - Visceral anatomy of an angler, Lophius piscatorius, ventral view. The digestive tract has been put away. ab.cav: abdominal cavity; c.oe: cut oesophagus; k: kidneys; v: ventricle. The black arrow indicates the anterior part of the specimen. Scale = 10 mm.
Figure 2 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 2. - The restricted gill opening (black arrow) in a few lophiiform and tetraodontiform species. A: Lophius piscatorius (Lophiiformes, Lophiidae); B: Microlophichthys micro- lophus (Lophiiformes, Oneirodidae); C: Tetraodon sp., (Tetraodontiformes, Tetraodontidae); D: Mola mola (Tetraodontiformes, Molidae). All drawings from F. Dejouannet, excepted drawing B modified after Trewavas and Regan (1932).
Figure 1 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 1. - Phylogenetic position of Tetraodontiformes and Lophiiformes (modified from Li (2008); note that in Dettaï and Lecointre (2008) tetraodontiforms and lophiiforms are sister-groups). Drawings from F. Dejouannet. 1: Angler (Lophius piscatorius, Lophiiformes, Lophiidae); 2: Puffer (Tetraodon sp., Tetraodontiformes, Tetraodontidae); 3: Ocean Sunfish (Mola mola, Tetraodontiformes, Molidae); 4: Boarfish (Capros aper, Caproidae); 5: Porgy (Sparus sp., Sparidae); 6: Perch (Perca sp., Percidae).
Figure 3 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy
Figure 3. - Visceral anatomy of a sea bream, Sparus aurata, left lateral view. ep.m: epaxial musculature; k: kidney; l: liver; sb: swimbladder. The arrow indicates the anterior part of the specimen. Scale = 10 mm.
Fig. 9 in Pneumaticity and soft-tissue reconstructions in the neck of diplodocid and dicraeosaurid sauropods
Fig. 9. Photographs and reconstructions of soft−tissues in the neck of Amargasaurus cazaui (MACN−N−15)), La Amarga, Neuquén, Argentina, La Amarga Formation, Hauterivian, Early Cretaceous. A. 7th and 8th cervical vertebra in left lateral (A) and in cranial aspects (A) and with close−up cranial view show1 2 ing crests at the cranial face of neural spines (A). B. Isolated cervical rib in dorsal (B) and ventral (B) aspects. C. Vertebral corpus of 5th cervical vertebra 3 1 2 in ventral aspect. D. 10th cervical vertebral in left lateral aspect. E. Transverse cross−sections through cervical vertebra in the diapophysis region, with internal extension of pneumatic cavities basing on Dicraeosaurus hansemanni (see also Fig. 8). Scale bars 60 mm, E is not to scale.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.