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FIG. 2 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 2. — General aspect of the specimens in transverse section at the same scale. The primary xylem is in dark grey, the secondary xylem – when present – is in black. A, MN201(slide MN201-E2); B, same specimen as A at a level of branching (slide MN201-F1); C, largest axis resulting from the branching of MN911 with two leaf bases (slide MN911-A1); D, same axis as in C at another level with one leaf base and the production of two traces from one arm of the stele (slide MN911-A2); E, smallest axis resulting from the branching of MN911 (slide MN911-A2); F, MN864 showing secondary xylem all around the stele (slide MN864-C1); G, KLC3 showing a small amount of secondary xylem (slide KLC3-C); H, KLC4 showing a small amount of secondary xylem like KLC3 but a much smaller cortex (slide KLC4-B2). Scale bar: 2 mm.
FIG. 1 in Anatomy, affinities, and evolutionary implications of new silicified stems of Sphenophyllum Brongniart, 1828 from the early Carboniferous (Mississippian) of France and Germany
FIG. 1. — Maps showing the location of the localities in Southern France (A) and Thuringia, Germany (B). Detailed maps modified from Galtier et al. 1988 and Meyer-Berthaud & Rowe 1997.
FIG. 2 in New remains of kollpaniine "condylarths" (Panameriungulata) from the early Palaeocene of Bolivia shed light on hypocone origins and molar proportions among ungulate-like placentals
FIG. 2. — Partial left mandible of Molinodus suarezi (MHNC 13867) bearing p3-m3: A, stereophotographs of the occlusal view; B, lingual view; C, labial view. Scale bar: 5 mm.
FIG. 4 in Fossil dipsadid snakes from the Guadeloupe Islands (French West-Indies) and their interactions with past human populations
FIG. 4. — Cranial bones of Alsophis antillensis (Schlegel, 1837) from La Désirade and Marie-Galante islands: A, right maxilla from Pointe Gros Rempart 6 (Dec. 7) located on La Désirade Island; B, right palatine from Blanchard Cave (Layer 8) located Marie-Galante Island; C, D, left pterygoid anterior (C) and posterior (D) fragments from Blanchard Cave (layers 8 and 10) located Marie-Galante Island; E, left compound bone from Blanchard Cave (Layer 8) located Marie-Galante Island; F, right dentary from Pointe Gros Rempart 6 (Dec. 3) located on La Désirade Island. Abbreviations: c. p., choanal process; d. n., dorsal notch; di., diastema; e. p. m., ectopterygoid process of the maxilla; e. p. p., ectopterygoid process of the pterygoid; f. m. n., foramen for the maxillary nerve; g. f., glenoid
FIG. 2 in Fossil dipsadid snakes from the Guadeloupe Islands (French West-Indies) and their interactions with past human populations
FIG. 2. — Morphological variability among four specimens of Alsophis Fitzinger, 1843. From left-to-right: smallest and largest available specimens of Alsophis rijgersmaei Cope, 1869 and Alsophis antillensis (Schlegel, 1837) varieties A and B (of Duméril et al. 1854). The two figured vertebrae for each specimen correspond to the most different morphologies observed among the trunk vertebrae (anterior vertebra on the left and median vertebra on the right).
FIG. 13. — A, B in New remains of kollpaniine "condylarths" (Panameriungulata) from the early Palaeocene of Bolivia shed light on hypocone origins and molar proportions among ungulate-like placentals
FIG. 13. — A, B, Lamegoia conodonta; C, didolodontidae indet.; A, occlusal view of a left m2 of Lamegoia conodonta (cast of holotype MNRJ 1463-V); B, occlusal view of a right M2 (reversed) of Lamegoia conodonta (cast of MNRJ 1465-V); C, occlusal view of a left M2 (cast of MNRJ 1464-V) of and undetermined didolodont (referred by Paula Couto [1952a] to L. conodonta). Scale bar: 5 mm.
FIG. 7 in Fossil dipsadid snakes from the Guadeloupe Islands (French West-Indies) and their interactions with past human populations
FIG. 7. — Results of statistical analyses of fossil and modern dipsadid snake vertebrae on the Guadeloupe Islands: A, two first axes of the PCA conducted on the maximum number of specimens (first analysis); B, Mahalanobis distance tree obtained from the results of the LDA (first analysis); C, two first axes of the PCA conducted on the maximum number of measurements (second analysis); D, Mahalanobis distance tree obtained from the results of the LDA (second analysis).
FIG. 12 in The Palaeotheriidae (Equoidea, Perissodactyla, Mammalia) from the Eocene fauna of Aumelas (Hérault department, France)
FIG. 12. — Strict consensus of the two trees of the cladistic analysis. "Hyracotheres" are included in the Palaeotheriidae according to Remy, 2017. The taxa recognized at Aumelas are mentioned in red.
FIG. 11 in The Palaeotheriidae (Equoidea, Perissodactyla, Mammalia) from the Eocene fauna of Aumelas (Hérault department, France)
FIG. 11. — Lophiotherium sp. from Aumelas: A, AUM 1633, right M3/; A1, occlusal view; A2, labial view; B, AUM 1547, left M2 (reversed), occlusal view; C, AUM 1626, left M2/ (reversed), occlusal view; D, AUM 234, right M1/, occlusal view (cast); E, AUM 232, left M1/ (reversed), occlusal view (cast); F, AUM 172, left M1/ (reversed), occlusal view; G, AUM 1550, right M/2, occlusal view (cast); H, AUM 1622, left M/1 (reversed), occlusal view; I, AUM 1624, right M/1, occlusal view; J, AUM 1551, right P/3, occlusal view (cast); K, AUM 1548, left mandible with (P/4)-M/1-M/3 (reversed); K1, occlusal view; K2, labial view; L, AUM 170, left mandible fragment with (alv. DP/1)-DP/2-DP/4 (reversed); L1, occlusal view; L2, labial view. Scale bars: 2 cm.
FIG. 5 in New remains of kollpaniine "condylarths" (Panameriungulata) from the early Palaeocene of Bolivia shed light on hypocone origins and molar proportions among ungulate-like placentals
FIG. 5. — Molinodus suarezi: partial maxilla (MHNC 13870): A, occlusal view; B, lingual view. Scale bar: 5 mm.
FIG. 50 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 50. — Lateral view of the right pelvic bones of some extant mysticetes. A, Balaenoptera musculus; B, Balaenoptera musculus; C, Megaptera novaeangliae; D, E, Balaena mysticetus. The iliac, pubic and ischial portions are, respectively, in blue, yellow and green. Modified from Struthers (1893).
FIG. 49 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 49. — Lateral view of innominate of some extinct cetaceans. A, Georgiacetus vogtlensis (GSM 350); B, Basilosaurus isis (CGM 42176, cast); C, Basilosaurus cetoides (USNM 12261); D, Chrysocetus healyorum (SCSM 87-195, cast, right innominate, reversed); E, Mystacodon selenensis (MUSM 1917). Not to scale.
FIG. 48 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 48. — Mystacodon selenensis (MUSM 1917, holotype). Left innominate: A, lateral view; B, dorsal view; C, medial view; D, ventral view. Scale bar: 5 cm.
FIG. 39 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 39. — Ribs transverse sections of Mystacodon, basilosaurids, and chaeomysticetes. A, Mystacodon selenensis (MUSM 1917, holotype): section of an anterior-median (right?) rib of the thoracic cage in the median region of the diaphysis; B, Dorudon atrox (UM 101222): section of a left R4 at mid-diaphysis (reversed); C, Basilosaurus isis (WH 074): section of a left R4 at mid-diaphysis. B and C are reproduced from Houssaye et al. (2015). D, Piscobalaena nana (MNHN.F. SAS1618). E, Balaenoptera acutorostrata (IRSNB uncatalogued). Abbreviations: ant, anterior; med, medial. Scale bar: 1 cm.
FIG. 42 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 42. — Mystacodon selenensis (MUSM 1917, holotype). Right humerus: A, lateral view; B, medial view; C, anterior view; D, posterior view. Scale bar: 5 cm.
FIG. 6 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 6. — Lateral view of the skull of Mystacodon selenensis (MUSM 1917, holotype). Oblique lines and grey-shaded regions indicate respectively broken and reconstructed parts. Scale bar: 20 cm.
FIG. 1 in Mystacodon selenensis, the earliest known toothed mysticete (Cetacea, Mammalia) from the late Eocene of Peru: anatomy, phylogeny, and feeding adaptations
FIG. 1. — Views of the extraction of the postcranial skeleton of Mystacodon selenensis (MUSM 1917 holotype) at Playa Media Luna (Ica Department, Peru).
FIG. 6 in Hungry for fruit? - A case study on the ecology of middle Miocene Moschidae (Mammalia, Ruminantia)
FIG. 6. — Bivariate plot with raw number of scratches versus raw number of pits in Micromeryx flourensianus Lartet, 1851 from Sansan () and Steinheim am Albuch (), in M.? eiselei Aiglstorfer, Costeur, Mennecart & Heizmann, 2017 (), and in Moschus moschiferus Linnaeus, 1758 () plotted in reference to extant leaf dominated ungulate browsers (B), and extant grazers (G) at 35 times magnification (extant comparative data from Semprebon 2002 and Solounias & Semprebon 2002). Gaussian confidence ellipses (p = 0.95) on the centroid are indicated for the extant leaf browsers and grazers (convex hulls) adjusted by sample size.
FIG. 2 in Hungry for fruit? - A case study on the ecology of middle Miocene Moschidae (Mammalia, Ruminantia)
FIG. 2. — Geographic position of the middle Miocene localities Sansan (France) and Steinheim am Albuch (Germany); palinspastic map for the middle Miocene in Central and Western Europe modified after Neubauer et al. (2015).
FIG. 1 in Hungry for fruit? - A case study on the ecology of middle Miocene Moschidae (Mammalia, Ruminantia)
FIG. 1. — Life reconstruction of Micromeryx Lartet, 1851 (based on male skeleton of Micromeryx? eiselei Aiglstorfer, Costeur, Mennecart & Heizmann, 2017; © SMNS).
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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.