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FIG. 4 in Charophyte flora from the Miocene of Zahle (Beeka Valley, Lebanon). Biostratigraphic, palaeoenvironmental and palaeobiogeographical implications
FIG. 4. — Biometric values of Chara aff. microcera Grambast & Paul, 1965 from sample Zahle 1 (n = 39 gyrogonites): A, gyrogonite height (µm); B, gyrogonite width (µm); C, number of convolutions visible in lateral view; D, isopolarity index (ISI = h/w × 100).
FIG. 8 in Charophyte flora from the Miocene of Zahle (Beeka Valley, Lebanon). Biostratigraphic, palaeoenvironmental and palaeobiogeographical implications
FIG. 8. — Biometric values of Nitellopsis (T.) merianii (Al. Braun ex Unger, 1852) Grambast & Soulié-Märsche, 1972 from sample Zahle 2 (n = 100 gyrogonites): A, gyrogonite height (µm); B, gyrogonite width (µm); C, number of convolutions visible in lateral view; D, isopolarity index (ISI = h/w × 100).
Fig. 12 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 12. Strict consensus of 432 most parsimonious trees depicting relationships among ornithomimosaur species derived from parsimony analysis of 220 characters in 50 coelurosaurian species (see http://research.amnh.org/users/norell/index.html). Tree statistics for shortest trees are (TL = 586, CI = 45, and RI =75). Continental distributions are listed after taxon names.
Fig. 11 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 11. Manus of Shenzhousaurus orientalis. ga, gastroliths; ldIIIu, left digit 3 ungual; rmcII, right metacarpal 2; rmcIII, right metacarpal 3; rpII1, right digit 2 first phalanx; rpII2, right digit 2 second phalanx; rpIII1, right digit 3 first phalanx; rpIII2, right digit 3 second phalanx; rpIII3, right digit 3 third phalanx, rdIu, right digit 1 ungual; rdIIu, right digit 2 ungual; rdIIIu, right digit 3 ungual.
Fig. 5 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 5. Closeup of braincase. Abbreviations: dv, dorsal vertebra; f, frontal; lp, left prootic, ls?, left laterosphenoid, lsa, left surangular, lsq, left squamosal; r, rib.
Fig. 4 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 4. Closeup of the left side of the skull of Shenzhousaurus orientalis. Abbreviations: ch, choana; fr, frontal; ld, left dentary; ll, left lacrimal; lmx, left maxilla; ln, left nasal; lpmx, left premaxilla; lsq, left squamosal; mxf, maxillary fenestra; plr, palatine recess; rn, right nasal.
Fig. 10 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 10. Pelvis of Shenzhousaurus orientalis. Abbreviations: ct, ectocondylar tuber; ft, fourth trochanter; gp, gastrocnemius process; gt, greater trochanter; lc, lateral crest; lf, left femur; lp, left pubis; li, left ilium; lis, left ischium; lt, lesser trochanter; mc, medial crest; o, obturator foramen; pb, pubic boot; rf, right femur, rp, right pubis; sac, sacrum.
Fig. 2 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 2. The holotype skeleton of Shenzhousaurus orientalis as preserved on the main block, with parts in counterblock reattached. Abbreviations: g, gastralia; ga, gastroliths; lf, left femur; li, left ilium; lis, left ischium; lp, left pubis; lu, ungual of left hand; pb, pubic boot; rdI, right digit I; rdII, right digit II; rdIII, right digit III; rf, right femur; rp, right pubis.
Fig. 9 in An Early Ostrich Dinosaur and Implications for Ornithomimosaur Phylogeny
Fig. 9. Gastroliths of Shenzhousaurus orientalis. ga, gastroliths; ldIIIu, left digit 3 ungual; lf, left femur; li, left ilium; rdI, right digit 3, rdII; right digit 2; rdIII, right digit 3.
FIG. 2. — Callicrypta chlamydea n. gen., n in A minute mid-Cretaceous flower from Siberia and implications for the problem of basal angiosperms
FIG. 2. — Callicrypta chlamydea n. gen., n. sp., a flower from the Cenomanian of Vilyuy Basin, Siberia, outline of the holotype (see Fig. 1A) showing interpretation of the floral parts. Abbreviations: C, carpel; Pi, inner petal; Po, outer petal; S, sepal; St, staminode?. Scale bar: 150 µm.
FIG. 2 in Biostratigraphie et lithologie des séries serravallo-tortoniennes du massif du Dahra et du bassin du Chélif (Algérie). Implications sur la position de la limite serravallo-tortonienne
FIG. 2. — Répartition biostratigraphique des foraminifères planctoniques de la coupe de Djebel Meni, bassin du Bas Chélif (Algérie). Abréviations: C, cinérites; h, horizon marno-calcaire; H, niveau à huîtres; S.D., surface durcie; S.R., surface de ravinement.
FIG. 4 in Biostratigraphie et lithologie des séries serravallo-tortoniennes du massif du Dahra et du bassin du Chélif (Algérie). Implications sur la position de la limite serravallo-tortonienne
FIG. 4. — Position de la limite serravallo-tortonienne et de la trangression tortonienne dans les massifs du Dahra et des Tessala (Algérie). Abréviations: S.D., surface durcie; S.R., surface de ravinement; * in Neurdin-Trescartes (1992).
FIG. 1 in Biostratigraphie et lithologie des séries serravallo-tortoniennes du massif du Dahra et du bassin du Chélif (Algérie). Implications sur la position de la limite serravallo-tortonienne
FIG. 1. — Localisation des coupes étudiées dans le bassin du Bas Chélif (Algérie): 1, Djebel Meni; 2, Koudiet Radjel el Meïda; 3, Sidi Moussa; 4, Oued Tangroutah; 5, coupe de Sidi Rahlem (Neurdin-Trescartes 1992); grisé, terrains anténéogène.
FIG. 4 in A minute mid-Cretaceous flower from Siberia and implications for the problem of basal angiosperms
FIG. 4. — Freyantha sibirica Krassilov et Golovneva (2001), from the Cenomanian of Tschulymo-Yenisey Basin, Siberia, inflorescence of staminate flowers subtended by calyptrate bracts with a prominent nectar gland (n). Scale bar: 1.5 mm.
FIG. 3 in A minute mid-Cretaceous flower from Siberia and implications for the problem of basal angiosperms
FIG. 3. — Pollen grains adhering to the petals and carpels of Callicrypta n. gen., n. sp., a pistillate flower from the Cenomanian of Vilyuy Basin, Siberia; A, polar aspect; B, oblique equatoriopolar aspect; C, lateral aspect. Scale bars: 3 µm.
FIG. 1. — Callicrypta chlamydea n. gen., n in A minute mid-Cretaceous flower from Siberia and implications for the problem of basal angiosperms
FIG. 1. — Callicrypta chlamydea n. gen., n. sp. from the Cenomanian of Vilyuy Basin, Siberia, SEM photographs; A, holotype, a pistillate flower with a calyx, biseriate corolla, and apocarpous gynoecium (see Fig. 2 for interpretation); B, carpel with a short style, abaxial aspect; C, radial sequence of sepal (S), outer petal (Po), inner petal (Pi) and carpel (C), the carpel is split in the median plane showing the locule, the position of papillate gland on the inner petal is marked as n; D, tubular structure (staminode?) clasped at base by the inner petal; E, papillate gland (nectary?) below the apical notch of an inner petal (see n); F, carpel, lateral view, style missing. Scale bars: A, 300 µm; B, 120 µm; C, 90 µm; D, 40 µm; E, 21 µm; F, 70 µm.
FIG. 4 in Alicornops (Mammalia, Rhinocerotidae) dans le Miocène supérieur des Collines Bugti (Balouchistan, Pakistan): implications phylogénétiques
FIG. 4. — Arbre de consensus strict des six arbres également parcimonieux (1330 pas; IC = 0,2639; IR = 0,4745) obtenus avec Hsearch de PAUP 4.0b10 (« stepwise addition », 100 réplications; Swofford 1998). Les nombres encerclés (de 1 à 22) sont les numéros des noeuds. Les nombres situés au-dessous des branches correspondent aux valeurs de bootstrap (500 réplications; commande Bootstrap de PAUP 4.0b10; Swofford 1998). Les espèces dont l'attribution générique est discutée dans le texte apparaissent en caractères gras. Abréviations: Ea, Elasmotheriina; Ma, Menoceratina.
FIG. 3 in Alicornops (Mammalia, Rhinocerotidae) dans le Miocène supérieur des Collines Bugti (Balouchistan, Pakistan): implications phylogénétiques
FIG. 3. — Alicornops complanatum (Heissig, 1972) n. comb., rangée dentaire inférieure gauche, avec p2-m3 (MNHN-MHNT Pak 1606), Sartaaf, Miocène supérieur des Collines Bugti (Balouchistan, Pakistan); A, vue occlusale; B, vue labiale. Échelle: 2 cm.
FIG. 2 in Alicornops (Mammalia, Rhinocerotidae) dans le Miocène supérieur des Collines Bugti (Balouchistan, Pakistan): implications phylogénétiques
FIG. 2. — Coupe synthétique du Néogène du Synclinal de Dera Bugti (Collines Bugti, Balouchistan, Pakistan). Le gisement de Sartaaf est indiqué par une flèche. Complété d'après Welcomme et al. (1997, 1999, 2001).
Fig. 8 in The Phylogenetic Resolving Power of Discrete Dental Morphology Among Extant Hedgehogs and the Implications for Their Fossil Record
Fig. 8. An example of ambiguous distribution of character states; (a) I2 cuspules always present in the juveniles and polymorphic for the adults (Hylomys suillus); (b) expression of the P3 posterior cingulum is a consequence of wear (Erinaceus amurensis).
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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.