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Fig. 1 in The Barremian heteromorph ammonite Dissimilites from northern Italy: Taxonomy and evolutionary implications
Fig. 1. Locality maps of the study area. A. Location of South Tyrol in northern Italy and Puez area (black star) and neighbouring La Stua section white star) within the Dolomites. B. Position of the Puez and La Stua localities on the Trento Plateau.
Fig. 5 in The Barremian heteromorph ammonite Dissimilites from northern Italy: Taxonomy and evolutionary implications
Fig. 5. Ranges of ancyloceratid ammonoids occurring in the Puez sections (P1 and P7) with indicated biostratigraphic ammonite zonation from Upper Hauterivian and Barremian. Distribution and range of Dissimilites species from Puez and all known occurrences worldwide. 1, this paper; 2, Lukeneder 2012; 3, Lukeneder and Aspmair 2006; 4, Company et al. 2008; 5, Company et al. 1995; 6, Vermeulen, 2005; 2006; 7, Vermeulen 1995, 1998; Ebbo et al. 2000; 8, Ebbo et al. 2000; 9, Busnardo 1963; 10, d'Orbigny 1842, 1852; Busnardo 2006; 11, Kilian 1910; 12, Vermeulen 2009; 13, Bert 2009; 14, Bert et al. 2010; 15, Uhlig 1887; 16, Haug 1887; 17, Haug 1889; 18, Stöhr 1993; 19, Cecca and Pallini 1994; 20, Uhlig 1883; 21, Vašíček 2006; 22, Nagy 1967; 23, Fülöp 1960; Fözy and Janssen 2009; 24, Simionescu 1998; 25, Avram 1976; 26, Avram 1994; 27, Avram 2001; 28, Breskovski 1966, 1975; 29, Dimitrova 1967; 30, Obata and Matsukawa 2007. Note indicated biostratigraphic ammonite zonation. Ammonite occurrences and ranges are marked by solid black circles. Bold horizontal line, stage boundary; dashed horizontal lines, zonal boundaries; dotted horizontal lines, subzonal boundaries. Taxonomic abbreviations: Ps., Pseudothurmannia; T., Taveraidiscus; K., Kotetishvilia; N., Nicklesia; hu., hugii; nic., nicklesi; pul., pulchella; com., compressissima.
Fig. 3 in A new turtle species of Brodiechelys from the Early Cretaceous of Spain: Systematic and palaeobiogeographic implications
Fig. 3. Phylogenetic hypotheses of the new taxon Brodiechelys royoi based on the modified data set of Sterli and de la Fuente (2011) proposed here (A), and on the data matrix proposed by Tong et al. (2012) (B). Values refer percentages under 100% obtained in the majority rule analyses.
Fig. 2 in A new turtle species of Brodiechelys from the Early Cretaceous of Spain: Systematic and palaeobiogeographic implications
Fig. 2. Type specimens of Brodiechelys royoi sp. nov. from Morella (Castellón, Spain). A. CMP-3b/181, holotype, shell in dorsal (A1, A2) and ventral (A3, A4) views. B. CMP-3c/293, second right costal plate in dorsal (B1, B2) and ventral (B3, B4) views. C. CMP-3c/122, first right costal in dorsal (C1, C2) and ventral (C3, C4) views.
Fig. 7 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 7. Details of limb bone microstructure of the ichthyopterygian Utatsusaurus hataii Shikama, Kamei, and Murata, 1978, NSM-VP-21865 (Osawa Formation, Spathian; Miyagi Prefecture, Japan). A, B. Mid-diaphyseal section of the radius (see Fig. 2F). C, D. The same section as A, close-up views of inner C) and outer (D) periosteal bone of the radius. E. Cortex of a phalanx (see Fig. 2G). F. The same section as E, close-up view of cortex. Photographed under natural light (A, C, D, F), polarized light without lambda compensator (B), and polarized light with lambda compensator (E).
Fig. 3 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 3. Transverse sections of dorsal ribs of the ichthyopterygian Utatsusaurus hataii Shikama, Kamei, and Murata, 1978 (Osawa Formation, Spathian; Miyagi Prefecture, Japan). A, B. NSM-VP-21865, proximal sections; A (see Fig. 2A) and B (see Fig. 2D, upper section). C. NSM-VP-20028, mid-shaft section (see Fig. 2B). D. NSM-VP-21865, mid-shaft section (see Fig. 2D, middle section). E. NSM-VP-20028, distal section (see Fig. 2C). F. NSM- VP-21865, distal section (see Fig. 2D, lower section). Photographed under natural light. Scale bars 1 mm.
Fig. 1 in A new turtle species of Brodiechelys from the Early Cretaceous of Spain: Systematic and palaeobiogeographic implications
Fig. 1. Geographical location of Morella (Castellón, Spain), the type locality of Brodiechelys royoi.
Fig. 6 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 6. Details of bone microstructure of a humerus (see Fig. 2E) of the ichthyopterygian Utatsusaurus hataii Shikama, Kamei, and Murata, 1978, NSM- VP-21865 (Osawa Formation, Spathian; Miyagi Prefecture, Japan). A, B. Periosteal cortex of mid-diaphyseal section. C. Close-up view of cell lacunae in the periosteal cortex. D. Close-up view of primary osteons in the primary periosteal bone. E. Mid-diaphyseal section, internal part of the shaft region. F, G. Cortex of the anterior flange. Photographed under natural light (A, C, D, F), polarized light without lambda compensator (B, G), and polarized light with lambda compensator (E).
Fig. 5 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 5. Mid-diaphyseal sections of limb bones of the ichthyopterygian Utatsusaurus hataii Shikama, Kamei, and Murata, 1978, NSM-VP-21865 (Osawa Formation, Spathian; Miyagi Prefecture, Japan). A. Humerus (see Fig. 2E). B. Radius (see Fig. 2F). C. Phalange (see Fig. 2G). Photographed under natural light. Scale bars 2mm.
Fig. 2 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 2. Analysed skeletal elements of the ichthyopterygian Utatsusaurus hataii Shikama, Kamei, and Murata, 1978 (Osawa Formation, Spathian; Miyagi Prefecture, Japan). A, D. NSM-VP-21865, dorsal ribs. B, C. NSM- VP-20028, dorsal ribs. E–G. NSM-VP-21865, humerus (E), radius (F), and phalanx (G).The humerus shows a D-shaped outline, consisting of the anterior flange (af) and the shaft region (sr). Grey quadrangles and white lines show the sectional planes. Scale bars 10 mm.
Fig. 4 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 4. Details of dorsal rib microstructure of the ichthyopterygian Utatsusaurus hataii Shikama, Kamei, and Murata, 1978 (Osawa Formation, Spathian; Miyagi Prefecture, Japan). A, B. NSM-VP-21865, proximal section (see Fig. 2A). C. NSM-VP-20028, mid-diaphyseal section (see Fig. 2B). D, E. NSM- VP-21865, close-up views of cell lacunae in the inner (D) and outer (E) cortices of proximal dorsal rib (see Fig. 2D). F. NSM-VP-20028, distal section (Fig. 2C). Photographed under natural light (A, C–F) and polarized light without lambda compensator (B).
Fig. 1 in Osteohistology of the Early Triassic ichthyopterygian reptile Utatsusaurus hataii: Implications for early ichthyosaur biology
Fig. 1. Simplified view of the evolution of the Ichthyopterygia. A. Time-calibrated phylogenetic tree of the Ichthyopterygia. B–D. Schematic drawings from McGowan and Motani 2003) showing the evolution of the body plan within the Ichthyopterygia (not to scale), between the basal ichthyopterygian Utatsusaurus (B), the basal ichthyosaurian Mixosaurus (C), and the scombrid fish-shaped neoichthyosaurian Ophthalmosaurus (D). Stratigraphic data compiled after McGowan and Motani (2003), Fernández (2003), Bennett et al. (2012), and Wiman (1910).
Fig. 11 in A unique late Eocene coleoid cephalopod Mississaepia from Mississippi, USA: New data on cuttlebone structure, and their phylogenetic implications
Fig. 11. Cuttlebone of sepioid cephalopod Mississaepia mississippiensis Weaver, Dockery III, and Ciampaglio, 2010; late Eocene, Mississippi, USA (A–C) and contemporary Sepia (D). A. MGS 1956. B. MGS 1956. C. MGS 1956. D. NRM−PZ Mo. 180818. Photographs (A1−D1); EDS data on chemical composition shows presence of: A2, high content of nitrogen indicating organic ingredient in silicified tissue preserved along contact between conotheca and septum; B2, nitrogen indicating organic ingredient of phosphatised sheet within the dorsal shield; C2, D2, nitrogen indicating organic ingredient of dorsal shield.
Fig. 10 in A unique late Eocene coleoid cephalopod Mississaepia from Mississippi, USA: New data on cuttlebone structure, and their phylogenetic implications
Fig. 10. Sepioid cephalopod Mississaepia mississippiensis Weaver, Dockery III, and Ciampaglio, 2010 (MGS 1963); late Eocene, Mississippi, USA. Mural part of septum lining a chamber (A), adoral surface of peripheral portion of septum (B), photographs (A1, B1); EDS data to show chemical composition (A2, B2); in both cases nitrogen indicates organic ingredient and phosphorus indicates diagenetic phosphatization of apparently originally organic material.
Fig. 4 in A unique late Eocene coleoid cephalopod Mississaepia from Mississippi, USA: New data on cuttlebone structure, and their phylogenetic implications
Fig. 4. Sepioid cephalopod Mississaepia mississippiensis Weaver, Dockery III, and Ciampaglio, 2010 (MGS 1945); late Eocene, Mississippi, USA. Inner surface of the phragmocone exposing a small fragment of brownish transparent septum preserved. Abbreviatons: lwph, lateral wall of the phragmocone; mlad, median line indicating apertural direction; mlpd, median line indicating posterior direction; mpls, mural part of last septum; rr, ribby relief; sr, septal ridge; trs, transparent fragmentary septum; vsdsh, ventral side of dorsal shield.
Fig. 3 in A unique late Eocene coleoid cephalopod Mississaepia from Mississippi, USA: New data on cuttlebone structure, and their phylogenetic implications
Fig. 3. Sepioid cephalopod Mississaepia mississippiensis Weaver, Dockery III, and Ciampaglio, 2010 (MGS 1948); late Eocene, Mississippi, USA. Median cuttlebone section to show loosely mineralized dorsal shield (bottom), small cup−like protoconch covered by thin layer of the dorsal shield (on the left) and curved hollow phragmocone exhibiting two long chambers and next short chambers; to the right from the last preserved (eighth?) septum inner surface of phragmocone is transversely ribbed. Abbreviations: dsh dorsal shield; p, protoconch; rr, ribbed relief of the inner surface of the phragmocone; 1s, 2s, 3s, 8s, first, second, third, eighth septa.
Fig. 2 in A unique late Eocene coleoid cephalopod Mississaepia from Mississippi, USA: New data on cuttlebone structure, and their phylogenetic implications
Fig. 2. Sketch map showing the location of the Yazoo Clay, the Miss Lite Clay Pit in the northwest corner of the town of Jackson and the Moodys Branch Formation, Town Creek locality south of Jackson in Hinds County, Mississippi, USA.
Fig. 1 in A unique late Eocene coleoid cephalopod Mississaepia from Mississippi, USA: New data on cuttlebone structure, and their phylogenetic implications
Fig. 1. Cuttlebone of Late Eocene sepioid cephalopod Mississaepia mississippiensis Weaver, Dockery III, and Ciampaglio, 2010 from Mississippi, USA with a missing anterior−most part (MGS 1945), in left lateral (A) and ventral (B) views. Abbreviations: dsh, dorsal shield; lwph, lateral wall of the phragmocone; phr, phragmocone; vg, ventral groove of spine; vp, ventral plate.
Fig. 11 in Middle Cambrian gogiid echinoderms from Northeast Spain: Taxonomy, palaeoecology, and palaeogeographic implications
Fig. 11. Palaeogeographic distribution of gogiids in the early and middle Cambrian; reconstruction after McKerrow et al. (1992).
Fig. 9 in Middle Cambrian gogiid echinoderms from Northeast Spain: Taxonomy, palaeoecology, and palaeogeographic implications
Fig. 9. Eocrinoid blastozoan Gogia parsleyi Zamora sp. nov. A. Paratype MPZ2008/162. Complete juvenile specimen (length of theca is about 5 mm); brachioles are spiralled and probably show a 2−2 pattern. B. Paratype MPZ2006/558a. Advanced juvenile specimen (length of theca is 11 mm). C. Paratype MPZ2008/164b. Fragment of theca with tessellated plates, epispires with characteristic rim. D. Paratype MPZ2008/161, upper part of theca. Photographs are of latex casts taken from natural moulds whitened with NH4Cl.
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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.