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Fig. 1. A in Youngest record of the extinct walrus Ontocetus emmonsi from the Early Pleistocene of South Carolina and a review of North Atlantic walrus biochronology
Fig. 1. A. Map showing the location of South Carolina and Austin Sand Pit near Ridgeville in Dorchester County (asterisked). B. Generalized stratigraphic column of the Austin Sand Pit with biostratigraphically significant vertebrate fossils from the?Waccamaw Formation (C, D). Colors approximate sediments exposed in the Austin Sand Pit.
Fig. 3 in Youngest record of the extinct walrus Ontocetus emmonsi from the Early Pleistocene of South Carolina and a review of North Atlantic walrus biochronology
Fig. 3. Scatterplot of ratio of proximal transverse width/anteroposterior length versus radius of the arc of curvature for tusks of Odobenus and Ontocetus, including CCNHM 1144. Original plot modified from Kohno and Ray (2008: fig. 27).
Fig. 2 in The endocranial anatomy of the stem turtle Naomichelys speciosa from the Early Cretaceous of North America
Fig. 2. Cranial endocast, nasal cavity, and inner ear (plus cavum acustico-jugulare, A1 and blood vessels) of helochelydrid turtle Naomichelys speciosa Hay, 1908 (FMNH PR273) from the Early Cretaceous (Aptian/ Albian) Trinity Group, Texas; in right lateral (A1), right posterolateral (A2), dorsal (A3), and ventral (A4) views. 1, lateral branch of the internal carotid artery; 2, anteromedial branch of the carotid artery; 3, cerebral artery; 4,?unnamed branch of the nervi vidiani.
Fig. 3 in The endocranial anatomy of the stem turtle Naomichelys speciosa from the Early Cretaceous of North America
Fig. 3. Detail of the cranial endocast and blood vessels of helochelydrid turtle Naomichelys speciosa Hay, 1908 (FMNH PR273) in right lateroventral view. The image also includes the cavum acustico-jugulare, right inner ear, and cranial nerves V and VI. 1, lateral branch of the internal carotid artery; 2, anteromedial branch of the carotid artery; 3, cerebral artery; 4,?unnamed branch of the nervi vidiani. Not to scale.
Fig. 7 in A new species of glirid rodent Vasseuromys from the Aragonian (Miocene) of the Ebro Basin (north-eastern Spain)
Fig. 7. Ranges of size variation (in tenths of millimetres) in the upper dentition of Vasseuromys cristinae sp. nov., V. pannonicus, V. elegans, V. duplex, V. priscus, V. aff. elegans, V. sp., and V. aff. priscus. Localities for each taxon are shown in parentheses.
Fig. 6 in A new species of glirid rodent Vasseuromys from the Aragonian (Miocene) of the Ebro Basin (north-eastern Spain)
Fig. 6. Ranges of size variation (in tenths of millimetres) in the lower dentition of Vasseuromys cristinae sp. nov., V. pannonicus, V. elegans, V. duplex, V. bacchius, V. rugosus, V. priscus, and V.autolensis. Localities for each taxon are shown in parentheses.
Fig. 5 in A new species of glirid rodent Vasseuromys from the Aragonian (Miocene) of the Ebro Basin (north-eastern Spain)
Fig. 5. Ranges of size variation (in tenths of millimetres) in the upper dentition of Vasseuromys cristinae sp. nov., V. pannonicus, V. elegans, V. duplex, V. bacchius, V. rugosus, V. priscus, and V. autolensis. Localities for each taxon are shown in parentheses.
Fig. 3 in A new species of glirid rodent Vasseuromys from the Aragonian (Miocene) of the Ebro Basin (north-eastern Spain)
Fig. 3. Composite lithostratigraphic and magnetostratigraphic logs of the Tudela Formation (see Larrasoaña et al. 2006) and their correlation to the ATNTS2004 of Lourens et al. (2004). The position of PF2 is described in this study; for the other fossil localities see Fig. 1, Murelaga (2000) and Murelaga et al. (2004a, b).
Fig. 2 in A new species of glirid rodent Vasseuromys from the Aragonian (Miocene) of the Ebro Basin (north-eastern Spain)
Fig. 2. Geological map of the Lower–Middle Miocene continental sediments of the Tudela Formation exposed in the Bardenas Reales de Navarra area, showing the location of the Pico del Fraile 1 section and Pico del Fraile 2 (PF2). Other fossil localities studied previously by Murelaga (2000) and Murelaga et al. (2004a, b) are also shown. Abbreviations: BF1, Barranco del Fraile 1; BT3, Barranco de Tudela 3; CJ1, Cabezo de la Junta 1; CM1, Cabezo Marijuán 1; CV1, Cabezo Vaquero 1; N1, Nasa 1; N2, Nasa 3; N3, Nasa 3; PF1, Pico del Fraile 1; RB1, Rincón del Bu 1.
Fig. 1 in A new species of glirid rodent Vasseuromys from the Aragonian (Miocene) of the Ebro Basin (north-eastern Spain)
Fig. 1. Nomenclature of the cheek teeth, after Freudenthal (2004). A. Lower molars. B. Upper molars.
Fig. 8 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 8. Comparison of line−drawing reconstructions of skulls of Pachyrhinosaurus perotorum (A), Pachyrhinosaurus canadensis (B), and Pachyrhinosaurus lakustai (C) in left lateral and dorsal views. A. Based on DMNH 21200 and DMNH 22558. B. Based upon NMC 9485, NMC 9602 as shown in Langston (1975), and from Sampson and Loewen (2010). C. Derived from Currie et al. (2008). Gray fill indicates hypothetical morphology not preserved in currently known specimens of P. perotorum. Drawings not to scale.
Fig. 4 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 4. Centrosaurine ceratopsid Pachyrhinosaurus perotorum sp. nov., holotype (DMNH 21200); parietal in dorsal (A), ventral (B), and right lateral (C) views. D. Reconstruction of the posterior parietal frill based upon DMNH 21200 and a yet to be catalogued partial parietal with a P3 horn. Scale bars 10 cm.
Fig. 3 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 3. Labelled line drawings of Pachyrhinosaurus perotorum paratype (DMNH 22558) skull in left lateral (A), right lateral (B), dorsal (C), ventral (D), and anterior (E) views. Scale bars 10 cm.
Fig. 7 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 7. Results of phylogenetic analysis. One of three equally most parsimonious trees (length = 107, C.I. (consistency index) = 0.8131, R.I. (retention index) = 0.8291) from our analysis set upon the Late Cretaceous timescale. Ranges of ceratopsian taxa other than Pachyrhinosaurus perotorum from Sampson and Loewren (2010). Timescale dates derived from Walker and Geissman (2009). Solid thick bars indicate well constrained range of a taxon. Open thick bars indicate poorly constrained or estimated range of a taxon. Open circles at nodes indicate named node−defined clades. Arcs on branches indicate stem−defined lineage names. Divergence points on tree are arbitrarily drawn, and are not based on calculations of lineage divergence dates. Abbreviations: Cen., Cenomanian; Con., Coniacian; Dan., Danian; Pal., Paleocene; Sa., Santonian; Tur., Turonian.
Fig. 2 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 2. Centrosaurine ceratopsid Pachyrhinosaurus perotorum sp. nov., paratype (DMNH 22558); skull in left lateral (A), right lateral (B), dorsal (C), ventral (D), and anterior (E) views. Scale bars 10 cm.
Fig. 6 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 6. Results of phylogenetic analysis. Strict consensus of the three equally most parsimonious trees generated by our analysis (length = 107, C.I. (consistency index) = 0.8131, R.I. (retention index) = 0.8291). Numbers at nodes are Bremer support values / Bootstrap percentages recovered from 1000 replicates.
Fig. 5 in A new Maastrichtian species of the centrosaurine ceratopsid Pachyrhinosaurus from the North Slope of Alaska
Fig. 5. Centrosaurine ceratopsid Pachyrhinosaurus perotorum sp. nov., paratype (DMNH 21201); partial parietal preserving portion of right transverse parietal bar and anterior rim horn in dorsal (A), ventral (B), and right lateral (C) views. Scale bars 5 cm.
Fig. 8 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 8. Single most parsimonious tree derived from maximum parsimony analysis of 49 hadrosauroid species, highlighting the position of Saurolophus morrisi sp. nov. within saurolophine hadrosaurids. Numbers above the branches indicate decay indices (Bremer support), whereas those below indicate bootstrap frequencies. Lambeeosaurinae is collapsed into a single branch for clarity; lambeosaurine interrelationships recovered were identical to those in Fig. 7.
Fig. 1 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 1. Partial right postorbital of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2852), lower Maastrichtian Moreno Formation of San Benito County, California, USA, showing the autapomorphic ornamentation of its jugal process. Posterior (A) and right lateral (B) views.
Fig. 5 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 5. Appendicular elements of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2760, a subadult), lower Maastrichtian Moreno Formation of Panoche Hills, Fresno County, California, USA. A. Partial left scapula and coracoid in lateral view. B. Partially articulated forelimb elements. C. Proximal segment of right tibia in lateral view. D. Distal fragments of femora. E. Right metatarsal III in dorsal 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.