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Fig. 16 in The West African enigma: Systematics, evolution, and palaeobiogeography of cardiid bivalve Procardium
Fig. 16. Comparative rib cross-sections and rib sculpture for species of Procardium. Schematic drawings based on the third/fourth rib anterior to the midline, close to the margin of an adult shell. A. P. magnei sp. nov. B. P. jansseni sp. nov. (upper part of rib sculpure reconstructed). C. P. danubianum (rib sculpture undefined). D. P. kunstleri. E. P. aff. kunstleri. F. P. avisanense. G. P. diluvianum. H. P. indicum. Median rib, showing radial groove on rib top (H2). Note presence of microscopic granulations (white arrow) and secondary riblet in interspace (black arrow). Scale bar 5 mm.
Fig. 6 in The West African enigma: Systematics, evolution, and palaeobiogeography of cardiid bivalve Procardium
Fig. 6. Cardiid bivalve Procardium avisanense (Fontannes, 1879) from Tortonian (Miocene) of Cacela Velha, Portugal (A, B, E) and Serravallian (Miocene) of France, Salles, "Le Minoy"(C) and "l'Argileyre" (D). A. PH 20376, external view. B. PH 20376, external (B1) and internal (B2) views. C. PH 19296, internal (C1) and external (C2) views. D. RGM.794107.a, internal (D1) and external (D2) views. E. RGM.794104.c, detail of anterior sculpture. Scale bars: A–D, 50 mm; E, 10 mm.
Fig. 1 in Late Jurassic-Early Cretaceous oysters from Siberia: A systematic review
Fig. 1. Geographical position of the studied oysters locations: 1, Lopsiya River; 2, Tolya River; 3, Maurynya River; 4, Yatriya River; 5, Boyarka River; 6, Bol'shaya Romanikha River; 7, Dyabaka-Tari River (after Zakharov 1966; Zakharov and Mesezhnikov 1974).
Fig. 4 in Late Jurassic-Early Cretaceous oysters from Siberia: A systematic review
Fig. 4. Measurements of morphometric parameters of oyster shells. D1, distance between posterior adductor muscle scar and anterior valve margin; D2, distance between posterior adductor muscle scar and posterior valve margin; D3, distance between posterior adductor muscle scar and ventral margin; D4, distance between posterior adductor muscle scar and dorsal margin; H, shell height; HCF, herringbone cross-foliated structure; Hla, ligament area height; Hpam, posterior adductor muscle scar height; L, shell length; LA, ligament area; LV, left valve; Lab, anterior bourrelet length; Lla, ligament area length; Lpam, posterior adductor muscle scar length; Lpb, posterior bourrelet length; Lr, resilifer length; PAM, posterior adductor muscle scar; RF, regularly foliated structure; RV, right valve.
Fig. 8 in Late Jurassic-Early Cretaceous oysters from Siberia: A systematic review
Fig. 8. Gryphaeid oyster Pernostrea mesezhnikovi sp. nov., Lower Volgian, Lopsiya River, Northern Urals. A. TsSGM 2068/28, paratype, details of right valve sculpture: fine radial striae (A1), exterior with Gastrochaenolites (A2), interior (A3). B. TsSGM 2048/21, interior of right valve. C. TsSGM 2068/29, interior of right valve.
Fig. 9. Strict consensus tree from phylogenetic analysis under extended implied weighting with 21 in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 9. Strict consensus tree from phylogenetic analysis under extended implied weighting with 21 different values of k.
Fig. 8. Consensus trees from phylogenetic analyses under equal weights. A. Strict consensus tree. B. Reduced consensus tree. a in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 8. Consensus trees from phylogenetic analyses under equal weights. A. Strict consensus tree. B. Reduced consensus tree. a, Martinmiguelia fernandezi; b, Taubatherium paulacoutoi; c, Ancylocoelus frequens; d, Huilatherium pluriplicatum; e, Asmodeus petrasnerus; f, Colpodon antucoensis + C. propinquus.
Fig. 7. Homalodotheriid notoungulate Asmodeus from Argentina. A in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 7. Homalodotheriid notoungulate Asmodeus from Argentina. A. Asmodeus petrasnerus Seoane and Cerdeño, 2014, from Quebrada Fiera, Mendoza; Deseadan SALMA (late Oligocene), MCNAM-PV 4958, left calcaneum, anterior (A1), posterior (A2) and medial (A3) views. B. Asmodeus osborni Ameghino, 1894 from Santa Cruz; Deseadan SALMA (late Oligocene), MACN A 12327, holotype, right calcaneum, medial (B1) and anterior (B2) views.
Fig. 6 in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 6. Tarsal bones of leontiniid notoungulate Gualta cuyana Cerdeño and Vera, 2015 from Quebrada Fiera, Mendoza, Argentina; Deseadan SALMA (late Oligocene). A. MCNAM-PV 4891, right astragalus, anterior (A1), distal (A2), posterior (A3), and lateral (A4) views. B. MCNAM-PV 5035, left navicular, anterior face to the left, proximal (B1) and distal (B2) views.
Fig. 4 in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 4. Left carpals and metacarpal of leontiniid notoungulate Gualta cuyana Cerdeño and Vera, 2015 from Quebrada Fiera, Mendoza, Argentina; Deseadan SALMA (late Oligocene), MCNAM-PV 4696. A. Pyramidal, anterolateral (A1), medial (A2), proximal (A3), and distal (A4) views. B. Magnum, anterior B1), proximal (B2), lateral (B3), and medial (B4) views. C. Unciform, anterolateral (C1), proximal (C2), medial (C3), and distal (C4) views. D. Proximal fragment of McIII, proximal (D1) and lateral (D2) views. E. Magnum and unciform in anatomical position, proximal view. F. Pyramidal and unciform in anatomical position, anterolateral view.
Fig. 5 in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 5. Tibiae of leontiniid notoungulate Gualta cuyana Cerdeño and Vera, 2015 from Quebrada Fiera, Mendoza, Argentina; Deseadan SALMA (late Oligocene). A. MCNAM-PV 4094, posterior view. B. MCNAM-PV 4785, distal (B1) and posterior (B2) views. C. Tibia, MCNAM-PV 4785, in anterior view and astragalus, MCNAM-PV 4891, in distal view.
Fig. 3 in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 3. Toxodontidae gen. et sp. indet. from Quebrada Fiera, Mendoza, Argentina; Deseadan SALMA (late Oligocene), MCNAM-PV 3907, left calcaneum fragment, posterior (A) and anterior (B) views.
Fig. 2. Toxodontian notoungulates from South America. A–D in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 2. Toxodontian notoungulates from South America. A–D. Proadinotherium sp. from Quebrada Fiera, Mendoza, Argentina; Deseadan SALMA (late Oligocene). A. MCNAM-PV 4238, right M2, occlusal view. B. MCNAM-PV 4960, left m2, labial (B1) and occlusal (B2) views. C. MCNAM-PV 3843, left m3, lingual (C1), labial (C2), and occlusal (C3) views. D. MCNAM-PV 4085, right calcaneum, posterior (D1), medial (D2), and anterior (D3) views. E. Proadinotherium muensteri Ameghino, 1902 from Colhue Huapi lake, Chubut, Argentina; Colhuehuapian SALMA (early Miocene), MACN Pv-17576 (cast), left calcaneum, medial view. F. Rynchippus equinus Ameghino, 1897 (Notohippidae) from Salla, Bolivia; Deseadan SALMA (late Oligocene), YPM VP-52313, left calcaneum, anterior (F1) and posterior (F2) views. G. Proadinotherium sp. from Quebrada Fiera, Mendoza, Argentina; Deseadan SALMA (late Oligocene), MCNAM-PV 4215, right astragalus, anterior (G1), posterior (G2), distal (G3), and lateral (G4) views. H. Proadinotherium leptognathum Ameghino, 1894 from Santa Cruz, Argentina; Deseadan SALMA (late Oligocene), MACN A 12319, left astragalus, anterior view. I. "Morphippus imbricatus" Ameghino, 1897 (Notohippidae) from Sarmiento Formation, Chubut, Argentina; Deseadan SALMA (late Oligocene), MACN A 12100, left astragalus, anterior view.
Fig. 1 in New postcranial remains of large toxodontian notoungulates from the late Oligocene of Mendoza, Argentina and their systematic implications
Fig. 1. Google Earth view of Quebrada Fiera site (A). Location of the study area on the map of Argentina (C). Geographical location (asterisk) of the fossil locality (B).{fig. will be grayscale in printed version}
Fig. 2 in Morphological and systematic re-assessment of the late Oligocene "Halitherium" bellunense reveals a new crown group genus of Sirenia
Fig. 2. Cranial and dental elements of the dugongine sirenian Italosiren bellunensis (De Zigno, 1875) comb. nov. from Cavarzano, Italy; upper Chattian, late Oligocene. A. Left premaxilla (MGPD-19Z) in lateral (A1) and dorsal (A2) views. B. Parietal-supraoccipital skullcap (MGPD-18Z) in dorsal (B1) and posterior (B2) views. C. Outline drawing of left zygomatic process of squamosal (MGPD-22Z) and jugal (MGPD-7384Z) in lateral view; shaded area indicates missing part. D. Outline drawing of left zygomatic process of squamosal (MGPD-22Z) in dorsal view. E. Left maxillary fragment (MGPD-20/21Z) in occlusal view; dashed lines indicate the estimated outline of DP5, outlined area indicates portion of controversial interpretation and is considered here as representing remnants of the DP5 crown.
Fig. 2 in Systematic revision and phylogenetic assessment of the foraminiferal family Globivalvulinidae
Fig. 2. Graphic explanation of descriptive morphological characters on which the cladistic analysis is based. A. Danielita gailloti Altıner and Özkan-Altıner, 2010 (Altıner and Özkan-Altıner 2010: pl. 1: 3). B. Urushtenella latebrosa Pronina-Nestell, 2001 (Pronina-Nestell and Nestell 2001: pl. 5: 12). C. Koktjubina windsorensis (Mamet, 1970) (Mamet 1970: holotype, pl. 1: 11). D. Retroseptellina decrouezae (Köylüoglu and Altıner, 1989) (modified from Altıner and Özkan-Altıner 2001: fig. 2). E. Charliella rossae Altıner and Özkan-Altıner, 2001 (modified from Altıner and ÖzkanAltıner 2001: fig. 2). F. Urushtenella latebrosa Pronina-Nestell, 2001 (Pronina-Nestell and Nestell 2001: pl. 5: 12). G. Globivalvulina graeca Reichel, 1946 (modified from Altıner and Özkan-Altıner 2001: fig. 2). H. Paradagmarita monodi Lys in Lys and Marcoux, 1978 (Loeblich and Tappan 1987: holotype, pl. 230: 6). I. Globivalvulina bulloides (Brady, 1876) (Loeblich and Tappan 1987: pl. 230: 14). J. Paraglobivalvulina mira Reitlinger, 1965 (Loeblich and Tappan 1987: holotype, pl. 230: 10). K. Septoglobivalvulina distensa (Wang in Zhao et al., 1981) (Gaillot and Vachard 2007: pl. 37: 2). L. Paradagmaritopsis kobayashii Gaillot and Vachard, 2009 (Gaillot et al. 2009: holotype, fig. 6: 6). Not to scale.
Fig. 1 in Morphological and systematic re-assessment of the late Oligocene "Halitherium" bellunense reveals a new crown group genus of Sirenia
Fig. 1. Geographic location of Cavarzano, Valle delle Guglie, near Belluno, Italy (modified after Bosellini et al. 1981 and Dallanave et al. 2009). Asterisk indicates estimated type locality of Italosiren bellunensis.
Fig. 3 in Systematic revision and phylogenetic assessment of the foraminiferal family Globivalvulinidae
Fig. 3. Phylogenetic tree resulting from the cladistic analysis. Thick lines represent the known stratigraphic ranges of the considered taxa (dashed line indicates uncertain stratigraphic ranges). Nodes are numbered above branches. See text and Appendix 1 for details.
Fig. 1 in Systematic revision and phylogenetic assessment of the foraminiferal family Globivalvulinidae
Fig. 1. Graphic explanation of descriptive morphological characters on which the cladistic analysis is based. A. Charliella rossae Altıner and Özkan-Altıner, 2001 (Altıner and Özkan-Altıner 2001: pl. 1: 2). B. Danielita gailloti Altıner and Özkan-Altıner, 2010 (Altıner and Özkan-Altıner 2010: pl. 2: 20). C. Globivalvulina sp. 1 (Nestell and Nestell 2006: pl. 6: 1). D. Paradagmarita flabelliformis Zaninetti, Altıner, and Catal, 1981 (Altıner 1981: pl. 39: 1). E. Tenebrosella asturica Villa and Sanchez de Posada, 1986 (Villa and Sanchez de Posada 1986: holotype, pl. 1: 1). F. Verispira jelli Palmieri, 1988 in spiral (F1) and umbilical (F2) views (modified from Palmieri 1988: fig. 8). G. Dagmarita sp. (Nestell and Pronina 1997: pl. 1: 6). H. Labioglobivalvulina baudi Gaillot and Vachard, 2007 (Gaillot and Vachard 2007: holotype, pl. 12: 10). I. Louisettita elegantissima Altıner and Brönnimann, 1980 (Loeblich and Tappan 1987: holotype, pl. 231: 7). J. Paraglobivalvulinoides septulifer Zaninetti and Altıner, 1981 (Zaninetti and Altıner 1981: holotype, pl. 1: 15). K. Paraglobivalvulinoides septulifer Zaninetti and Altıner, 1981 (Zaninetti and Altıner 1981: pl. 1: 19). Area in gray in C and D indicates the second stage of coiling. Not to scale.
Fig. 2 in Systematic review of Neocavia from the Neogene of Argentina: Phylogenetic and evolutionary implications
Fig. 2. Measurements used in the comparative analysis A. Skull of Microcavia australis, Recent. B. Third left upper molar (M3) C. First right lower premolar (p4; anterior to left). Abbreviations: Cranial measurements: APB, anteromedial-posterorlateral length of tympanic bullae; APL, length of premaxillary-maxillary suture to anterior border of foramen magnum; BO, width of the anterior half of the basioccipital; BP, anteroposterior length of the posterior part of the diastema; IF, length of incisive foramina; MXL, length from the premaxillary-maxillary suture to the posterior portion of the M3 projection; UDL, upper diastema length from alveolar posterior margin of incisor to alveolar anterior margin of P4; WBc, width of basicranial. Dental measurements: LAP, anteroposterior length of molariforms; LLA, anteroposterior length of anterior lobe of molariforms; LPL, anteroposterior length of posterior lobe of molariforms; PLE, posterolabial extension of anterior lobes; WAL, mediolateral length of anterior lobe of molariforms; WPL, mediolateral length of posterior lobe of molariforms.
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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.