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Fig. 3 in Xenoxylon synecology and palaeoclimatic implications for the Mesozoic of Eurasia
Fig. 3. Number of data for each taxonomical wood group (for the composition of each taxonomical group see Table 2); LT, Late Triassic; EMJ, Early to Middle Jurassic; LJEK, Late Jurassic to Early Cretaceous; LK, Late Cretaceous.
Fig. 1. A in Xenoxylon synecology and palaeoclimatic implications for the Mesozoic of Eurasia
Fig. 1. A. In situ erect stump of Mesozoic Xenoxylon from Bayakodan, near Kuwajima in Shiraminemura, Japan. Used with the permission of Kazuo Terada (specimen no. 53901 in Suzuki and Terada 1992). B. Typical xenoxylean radial pitting and window-like cross-field pits in radial section of Xenoxylon (slide CBNU 73112).
Fig. 7 in Xenoxylon synecology and palaeoclimatic implications for the Mesozoic of Eurasia
Fig. 7. Diversity index (DI = GD/N, where GD is the number of genera associated with Xenoxylon, and N the number of occurrences) for each time period. Abbreviations: LT, Late Triassic; EMJ, Early to Middle Jurassic; LJEK, Late Jurassic to Early Cretaceous; LK, Late Cretaceous.
Fig. 14 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 14. Strict consensus of 34 trees. Length = 2219, CI = 0.2881, RI – 0.7500. 100 taxa are included. Goniopholididae are monophyletic, with Calsoyasuchus the most basal form. Goniopholis forms a paraphyletic group with respect to Anteophthalmosuchus. Sunosuchus is polyphyletic, spread among several groups including Eutretauranosuchus, Kansajsuchus, and the European goniopholidids. All European goniopholidids form a monophyletic group to the exclusion of the Asian and North American forms. Tomistoma and Gavialis cluster together to the exclusion of Alligator.
Fig. 7. Crocodylomorph Kansajsuchus extensus Efimov, 1975 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 7. Crocodylomorph Kansajsuchus extensus Efimov, 1975 frontoparietal region from the Santonian (Upper Cretaceous) of Fergana, Tajikistan, PIN 2399-308, in posterior (A), ventral (B), anterior (C), dorsal (D), and lateral (E) views, clearly demonstrating the trapezoidal shape of the skull roof, and the near-circular fenestrae.
Fig. 6. Crocodylomorph Kansajsuchus extensus Efimov, 1975 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 6. Crocodylomorph Kansajsuchus extensus Efimov, 1975 specimens from the Santonian (Upper Cretaceous) of Fergana, Tajikistan. A. Portion of frontal bone and posterior end of nasal, PIN 2399-310. B. Broken portion of a left maxilla, PIN 2399-307. C. Anterior section of right nasal bone, PIN 2399-306. D. Example of dorsal dermal osteoderm, PIN 2399-312. In ventral (A –D ) and dorsal (A –D ) views.
Fig. 1 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 1. Adult crocodylomorph "Sunosuchus" thailandicus Buffetaut and Ingavat, 1980, PIN 4174-1, from the Tithonian (Upper Jurassic) of Shar Teeg, Mongolia. A. Rostrum, quadrates, and occipital condyle in dorsal aspect. B, C. Rostrum and mandible in left (B) and right (C) views. Photographs (A 1 –C 1) and explanatory drawings (A –C ).
Fig. 13 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 13. Strict consensus of 324 trees. Length = 2305, CI = 0.2872, RI = 0.7497. 102 crocodilomorph taxa are included. The inclusion of "Sunosuchus" thailandicus and material formerly ascribed to Turanosuchus aralensis results in a large polytomy including Eusuchia, Goniopholididae, Pholidosauridae, and Metriorhynchidae. Relationships within Goniopholididae for the most part collapse. A notable exception is the association of Eutretauranosuchus and "Sunosuchus" junggarensis, which suggests that this is a very strongly supported relationship.
Fig. 2 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 2. Crocodylomorph "Sunosuchus" thailandicus Buffetaut and Ingavat, 1980 dentition, PIN 4174-1, from the Tithonian (Upper Jurassic) of Shar Teeg, Mongolia. A. Rostrum in palatal aspect. Photograph (A1) and explanatory drawing (A2). B. Anterior mandible in dorsal view, from symphysis to the anterior edge of the external mandibular fenestra.
Fig. 11 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 11. Poorly preserved mandibular symphysis of?Goniopholididae gen. et sp. indet. (previously Turanosuchus aralensis Efimov, 1988) from the Upper Cretaceous of Kazakhstan, PIN 2229-507, in dorsal view, with majority of tooth alveoli present but damaged. For full explanation see text.
Fig. 5. Crocodylomorph Kansajsuchus extensus Efimov, 1975 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 5. Crocodylomorph Kansajsuchus extensus Efimov, 1975, holotype, PIN 2399-301 from the Santonian (Upper Cretaceous) of Fergana, Tajikistan. Right premaxilla of an adult crocodilian in dorsal (A), lateral (B), and ventral (C) views. Photographs (A1–C1) and explanatory drawings (A2–C2).
Fig. 12 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 12.?Goniopholididae gen. et sp. indet. (previously Turanosuchus aralensis Efimov, 1988) from the Santonian (Upper Cretaceous) of the Zhirkindek Formation, Kazakhstan, material formerly attributed to Turanosuchus aralensis Efimov, 1988. A. Section of left dentary, PIN 2229-506, including two complete and two incomplete alveoli in dorsal (A1) and lateral (A2) views. B. Dermal osteoderm, PIN 2229-503, in dorsal (B1) and ventral (B2) views. C. Fragmented right maxilla, PIN 2229-502 (demonstrating the sinusoidal condition also seen in PIN 4174-1), in ventral (C1) and dorsal (C2) views. D. Posterior portion of left mandible, PIN 2229-501, in dorsal (D1), lateral (D2), and medial (D3) views.
Fig. 9. Crocodylomorph Kansajsuchus extensus Efimov, 1975 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 9. Crocodylomorph Kansajsuchus extensus Efimov, 1975 left angular region of the mandible. Specimens from the Santonian (Upper Cretaceous) of Fergana, Tajikistan, PIN 2399-453, in ventral (A), dorsal (B), medial (C), and lateral (D) views.
Fig. 8. Crocodylomorph Kansajsuchus extensus Efimov, 1975 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 8. Crocodylomorph Kansajsuchus extensus Efimov, 1975 basioccipital region and quadrate, preserving several nerve and vascular foramina. Specimens from the Santonian (Upper Cretaceous) of Fergana, Tajikistan. A. PIN 2399-308 (second part) in posterior (A1), ventral (A2), and dorsal (A3) views. B. PIN 2399-468, a quadrate in posterior (B1), dorsal (B2), and ventral (B3) views.
Fig. 3 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 3. Crocodylomorph "Sunosuchus" thailandicus Buffetaut and Ingavat, 1980, PIN 4174-1, from the Tithonian (Upper Jurassic) of Shar Teeg, Mongolia. Occipital condyle in lateral (A) and posterior (B) views.
Fig. 4 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 4. Teeth of crocodylomorphs from the Cretaceous of Central Asia. A. "Sunosuchus" thailandicus Buffetaut and Ingavat, 1980, left mandibular tooth of PIN 4174-1. Tooth is from mid-mandible and is similar in size to all of the other mandibular teeth, which show little size variation. B, C. Kansajsuchus extensus Efimov, 1975. B. Caniniform tooth of PIN 2399-313 in anterior (B1), posterior (B2), and lateral (B3) views. The tooth is characterized by prominent ridges, including a distinctive "double keel" on the posterior side of the tooth. The tooth is from the anterior part of the jaw. C. Molariform tooth of PIN 2399-314 in posterior (C1), anterior (C2), and lateral (C3) views. The tooth shares the ridges characteristic of Kansajsuchus, including a less prominent version of the double keel, but is blunter, and derived from the posterior part of the jaw.
Fig. 10. Crocodylomorph Kansajsuchus extensus Efimov, 1975 in A re-evaluation of goniopholidid crocodylomorph material from Central Asia: Biogeographic and phylogenetic implications
Fig. 10. Crocodylomorph Kansajsuchus extensus Efimov, 1975 postcranial material from the Santonian (Upper Cretaceous) of Fergana, Tajikistan. A. Cervical vertebra, PIN 2399-304, in anterior (A 1) and lateral (A 2) views. B. Left femur, PIN 2399-318, in posterior (B ) and lateral (B ) views.
Fig. 2 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 2. The glirid mammals Eliomys yevesi sp. nov. (A–L) and Eliomys intermedius Friant, 1953 (M–U) from Spain, Villatoya-Venta del Moro Formation, Miocene (see Table 1 for locality name abbreviations). A. VVmA-42 (MGUV-27256), right p4. B. VVmA-1 (MGUV-27215), right m1, m2. C. VVmA- 6 (MGUV-27220), right m1, m2. D. VVmBC-5 (MGUV-27490), right m3. E. VVmA-40 (MGUV-27254), left P4. F. VVmA-16 (MGUV-27230), right M1, M2. G. VVmA-25 (MGUV-27239), right M1, M2. H. VVmA-13 (MGUV-27227), left M3. I. VVmA-14 (MGUV-27228), left M3. J. ABS3A-38 (MGUV-23529), right m1, m2. K. AF1'06-190 (MGUV-28334), right m1, m2. L. AF1'07-36 (MGUV-28427), left M1, M2. M. AC0-88 (MGUV-28551), right m3. N. LB2B-176 (MGUV-28727), right m1, m2. O. LB2B-241 (MGUV-28727), left M1, M2. P. LB2B-177 (MGUV-28728), left M3. Q. LB2B- 178 (MGUV-28729), left P4. R. AL2D-290 (MGUV-28063), left m1, m2. S. AL2D-356 (MGUV-28129), left m3. T. AL2D-291 (MGUV-28064), right M1, M2. U. AL2D-293 (MGUV-28066), left M1, M2.
Fig. 1 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 1. Location of the Venta del Moro, Alcoy, Purcal, and Calicasas sites (stars) that have yielded specimens of Eliomys yevesi sp. nov. The dormouse symbol indicates the location of Venta del Moro, the type locality of E. yevesi. Abbreviations: ABS-3A, Alcoi Barranc Sud 3A; AF-1, Alcoi Forn 1; CLC-3B, Calicasas 3B; PUR-4, Purcal 4; VVm, Venta del Moro.
Fig. 5 in A new Eliomys from the Late Miocene of Spain and its implications for the phylogeny of the genus
Fig. 5. Early Vallesian (early Tortonian) to early Villanyan (Piacenzian) stratigraphic distribution and proposed phylogenetic relationships of the genus Eliomys (modified from García-Alix et al. 2008a). Abbreviations: ABS, Alcoi Barranc Sud; AC, Alcoy Cristian; AF, Alcoi Forn; AL, Alcoy; ALJ, Aljezar; ARQ, Arquillo; BLS, Barranco de Blas; CA/MN, Calatayud-Montalbán Basin; CB/AL, Cabriel and Alcoy Basins; CLC, Calicasas; DHS, Dehesa; ELMA, European Land Mammal Age; FOU, Lo Fournas; FRA, France; GER, Germany; GR/GU, Granada and Guadix Basins; HAU, Hautimagne; Ham, Hammerschmiede; LB, La Bullana; LC, Lomas de Casares; LG, La Gloria; LM, Los Mansuelos; MN, Mammal Neogene Units; ORR, Orrios; OTU, Otura; PE-2A, Pedregueras 2A; PUR, Purcal; SAR, Sarrión; SET, Sète; SOL, Solera; TCH, Tollo de Chiclana; TER, Teruel Basin; VAL, Villaba Alta; VVm, Venta del Moro; VP, Viveros de Pino. The double-headed arrow indicates the range of uncertainty.
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.