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Fig. 2. A in Pterosauria of the Great Oolite Group (Bathonian, Middle Jurassic) of Oxfordshire and Gloucestershire, England
Fig. 2. A. The holotype mandible ("Huxley 1859: fig. 2") of "Rhamphocephalus" bucklandi (Meyer, 1832) (nomen nudum) from Taynton Limestone Formation (Bathonian, Middle Jurassic), Stonesfield, Oxfordshire, UK, which has since gone missing and is presumed lost. B. The holotype mandible (GSM 113723) of "Rhamphocephalus" depressirostris Huxley, 1859 from Fuller's Earth Formation (Bathonian, Middle Jurassic), Smith's Quarry, Sarsden, Chipping Norton, Oxfordshire, UK. Both after Huxley (1859: figs. 1a/1b and 2 respectively). No scales in the original figures.
Fig. 2 in Paoliida, a Putative Stem-Group of Winged Insects: Morphology of New Taxa from the Upper Carboniferous of Poland
Fig. 2. Line drawings of paoliid insect Zdenekia silesiensis sp. nov., Załęże beds, Mudstone series (Langsettian, Upper Carboniferous), SosnowiecKlimontów, Upper Silesian Coal Basin, Poland (after Kukalová−Peck 1991). A. Fore wing holotype specimen MP ISEA I−F/MP/1488/2ab/08. B. Fore wing paratype specimen MP ISEA I−F/MP/1540/25/09. C. Hind wing specimen MP ISEA I−F/MP/1488/3/08.Vein symbols are abbreviated as follows: ScP, Subcosta posterior; RA/RP, Radius anterior/posterior; MP, Media posterior; CuA/CuP, Cubitus anterior/posterior; AA/AP, Analis anterior/posterior.
Fig. 5 in Ammonoid biodiversity changes across the Cenomanian-Turonian boundary in the Yezo Group, Hokkaido, Japan
Fig. 5. Temporal changes in faunal components of ammonoid species richness in the Mikasa area. Abbreviations: CIUs, carbon isotopic units; e., early; m., middle.
Fig. 1. A in Paoliida, a Putative Stem-Group of Winged Insects: Morphology of New Taxa from the Upper Carboniferous of Poland
Fig. 1. A. Geographical situation and geological map of the Upper Silesian Coal Basin with position of insect localities: Horní Suchá (Czech Republic) and Sosnowiec (Poland) indicated by white asterisks (modified after Jureczka et al. 1995). B. Lithostratigraphic division of Pennsylvanian strata of Czech and Polish parts of the Upper Silesian Coal Basin after Dopita et al. (1997) with corresponding stratigraphical levels of both localities indicated by white asterisks. Abbreviations: Bolsov., Bolsovian; Duckman., Duckmantian.
Fig. 4 in Ammonoid biodiversity changes across the Cenomanian-Turonian boundary in the Yezo Group, Hokkaido, Japan
Fig. 4. Temporal changes in ammonoid species richness, extinction, and origination rates in the Mikasa, Obira, and Oyubari areas. Abbreviations: CIUs, carbon isotopic units; CTBE, Cenomanian–Turonian boundary event; e., early; m., middle.
Fig. 2 in Ammonoid biodiversity changes across the Cenomanian-Turonian boundary in the Yezo Group, Hokkaido, Japan
Fig. 2. Composite columnar sections in the Mikasa (A), Obira (B), and Oyubari (C) areas and the stratigraphical levels of macrofossil datum planes used in the present study. The shaded portion shows the Cenomanian–Turonian boundary event (CTBE). The molluscan fossil data are from Tanabe et al. (1977), Futakami (1986), Kurihara and Kawabe (2003), Funaki and Hirano (2004), Kurihara et al. (2007) and unpublished original data. The planktonic foraminiferal zonation and the CTBE are from Hasegawa (1997, 1999), Nishi et al. (2003), Kurihara (2006), and Uramoto et al. (2007, 2009). Abbreviations: Ka, Katsurazawa Formation; Hk, Hikagenosawa Formation; mdst, mudstone; sdst, sandstone; A. nipponicus, Actinoceramus nipponicus; Hel. helvetica, Helvetoglobotruncana helvetica; I. hobetsensis, Inoceramus hobetsensis nonsulcatus; I. kamuy, Inoceramus kamuy; W. arc., Whiteinella archaeocretacea.
Fig. 3 in Ammonoid biodiversity changes across the Cenomanian-Turonian boundary in the Yezo Group, Hokkaido, Japan
Fig. 3. Correlation of Upper Cretaceous δ13C stratigraphy of terrestrial organic materials in the Mikasa, Obira, and Oyubari areas, Japan and reference δ13C stratigraphy of carbonates in Europe (after Jarvis et al. 2006). Six carbon isotopic units (CIUs) were identified in the present study. Abbreviations: e., early; m., middle; PDB, Pee Dee Belemnite Standard; Aj, Acanthoceras jukesbrownei; An, Actinoceramus nipponicus; Ar, Acanthoceras rhotomagense; Ca, Calycoceras spp.; Cg, Calycoceras guerangeri; Ci, Cunningtoniceras inertme; Cu, Cunningtoniceras spp.; Cw, Collignoniceras woollgari; Fc, Fagesia catinus; Ih, Inoceramus hobetsensis; Ik, Inoceramus kamuy; Md, Mantelliceras dixoni; Mg, Metoicoceras geslinianum; Mn, Mammites nodosoides; Nj, Neocardioceras juddii; Wd, Watinoceras devonense.
Fig. 4 in A new deinonychosaurian track from the Lower Cretaceous Hekou Group, Gansu Province, China
Fig. 4. Turning trackway of Dromaeosauripus yongjingensis GSLTZPS2−TB at Liujiaxia Dinosaur National Geopark site II, Early Cretaceous. A. Photograph. B. Outline drawing. C. Pace angulations.
Fig. 5 in A new deinonychosaurian track from the Lower Cretaceous Hekou Group, Gansu Province, China
Fig. 5. Schematic map of the relative positions of six Dromaeosauripus yongjingensis trackways (GSLTZP−S2−TA to TF) at Liujiaxia Dinosaur National Geopark site II, Early Cretaceous.
Fig. 2. Deinonychosaurian track Dromaeosauripus yongjingensis ichnosp. nov. holotype GSLTZPS2 in A new deinonychosaurian track from the Lower Cretaceous Hekou Group, Gansu Province, China
Fig. 2. Deinonychosaurian track Dromaeosauripus yongjingensis ichnosp. nov. holotype GSLTZPS2−TE4L from the Early Cretaceous Yanguoxia track site, Gansu, China. A. Photograph. B. Com− puterized photogrammetry, with 0.2 mm contour lines; color banding reflects topography (blue− green, highest; red−white, lowest). Based on the photogrammetric maps from Xing et al. (2009: fig. 6). C. Outline drawing.
Fig. 6 in A new deinonychosaurian track from the Lower Cretaceous Hekou Group, Gansu Province, China
Fig. 6. Schematic diagrams of dromaeopodid ichnotaxa to the same scale. A. Menglongipus (Xing et al. 2009). B. Shandong Velociraptorichnus (Li et al. 2007). C. Velociraptorichnus (Zhen et al. 1994; Xing et al. 2009). D. Dromaeosauripus yongjingensis (this study). E. Dromaeosauripus hamanensis (Kim et al. 2008). F. Dromaeopodus (Li et al. 2007). G. Paravipus (Mudroch et al. 2010). H. Morocco didactyl track (based on Ishigaki and Lockley 2010).
Fig. 2 in The diversity of cimolestan mammals within the White River Group of South Dakota and Nebraska
Fig. 2. Right mandible of the cimolestan mammal gen. et sp. indet. (FMNH UC 349) from the White River Badlands of South Dakota, Late Eocene– Early Oligocene, in dorsal (A) and buccal (B) views.
Fig. 1 in The diversity of cimolestan mammals within the White River Group of South Dakota and Nebraska
Fig. 1. Photographs of the back of the hillside (A) and the front face of the hillside (B) on which locality BADL-LOC-0236 (Badlands National Park, South Dakota, USA; Rupelian, Oligocene) is located, with Units 1–6 labeled (Unit 2 dashed, because its presence is not laterally continuous throughout the locality). C. Stratigraphic column based on A.
Fig. 3 in The diversity of cimolestan mammals within the White River Group of South Dakota and Nebraska
Fig. 3. Anterior portion of a mammalian mandible (BADL 16917) here tentatively referred to Chadronia sp., from the lower Scenic Member of the Brule Formation, South Dakota, in left buccal (A), dorsal (B), ventral (C), and anterior (D) views. Photographs (A1, B1, C, D) and explanatory drawings (A2, B2)
Fig. 3 in Early Cambrian "soft-shelled" brachiopods as possible stem-group phoronids
Fig. 3. Schematic reconstruction of lingullotretid brachiopod Lingulosacculus nuda gen. et sp. nov. Abbreviation: ap, anterior projection.
Fig. 2 in Early Cambrian "soft-shelled" brachiopods as possible stem-group phoronids
Fig. 2. Anterior portion of lingullotretid brachiopod Lingulosacculus nuda gen. et sp. nov. (GSC−34952) in low−angle light, showing lophophore arms.
Fig. 1 in Early Cambrian "soft-shelled" brachiopods as possible stem-group phoronids
Fig. 1. Light micrographs (A1, B1) and camera lucida drawings (A2, B2) of lingullotretid brachiopod Lingulosacculus nuda gen. et sp. nov. A. GSC−34952, with the smaller oval−shaped dorsal valve superimposed on the larger coniform ventral valve. B. GSC−34953 (holotype), with the smaller dorsal valve largely obscured by the superimposed ventral valve; white arrows in B1 indicate the margins of the propareas on the ventral pseudointerarea.
Fig. 7 in Early Cretaceous multituberculate mammals from the Kuwajima Formation (Tetori Group), central Japan
Fig. 7. Eobatarid multituberculate mammal Hakusanobaatar matsuoi gen. et sp. nov.; Lower Cretaceous Kuwajima Formation, Shiramine, Japan; SEM photograph of SBEI 2352 (a resin cast of SBEI 581 before the anterior part of the dentary was lost), left lower jaw fragment with damaged p4. A. Lingual view. B. Labial view; arrows indicate alveoli of a single−rooted p2 and a double−rooted p3. C. Occlusal view; arrows indicate the alveolus of a p2 and the anterior alveolus of a p3.
Fig. 2 in Early Cretaceous multituberculate mammals from the Kuwajima Formation (Tetori Group), central Japan
Fig. 2. Eobatarid multituberculate mammal Hakusanobaatar matsuoi gen. et sp. nov., SBEI 1736, holotype; Lower Cretaceous Kuwajima Formation, Shiramine, Japan. SEM photograph of resin casts. A. Left upper dentition; A1, labial view (I3, P1–P5 and the base of I2); A2, occlusal view (only cheek teeth), left to anterior. B. Isolated right M1, postero−labial view. C. Right lower jaw fragment with p3 and p4, labial view.
Fig. 3 in Early Cretaceous multituberculate mammals from the Kuwajima Formation (Tetori Group), central Japan
Fig. 3. Eobatarid multituberculate mammal Hakusanobaatar matsuoi gen. et sp. nov., SBEI 1736holotype; Lower Cretaceous Kuwajima Formation, Shiramine, Japan. A. Left upper dentition; A1, I3 and P1 to P5 in labial view; A2, I3 in anterior view; A3, P5 in lingual view, right to anterior; A4, P1 to P4 in occlusal view, left to anterior; A5, P5 in occlusal view, left to anterior. B. Isolated left M1; B1, in labial view; B2, in occlusal view, left to anterior. C. Isolated I2 in lateral view.
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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.