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Fig. 14 in A taxonomic revision of the Neotropical electric fish genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with descriptions of 15 new species
Fig. 14. Collection records for Brachyhypopomus bennetti (circles), B. cunia (squares), and B. diazi (triangles). Holotype locations for B. bennetti and B. cunia, and location of lost holotype for B. diazi are marked with open symbols. Elevation data refers to altitude above mean sea level (see Fig. 2 for legend).
Fig. 5 in A taxonomic revision of the Neotropical electric fish genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with descriptions of 15 new species
Fig. 5. Collection records for Brachyhypopomus alberti (circles), B. batesi (squares), and B. benjamini (triangles). Holotype locations are marked with open symbols. Elevation data refers to altitude above mean sea level (see Fig. 2 for legend).
Fig. 13. Brachyhypopomus bennetti. a. MCP 47021 in A taxonomic revision of the Neotropical electric fish genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with descriptions of 15 new species
Fig. 13. Brachyhypopomus bennetti. a. MCP 47021 (WC13.160893), female, 158 mm TL (head in lateral view, and body in lateral and dorsal views, specimen fixed in formalin and preserved in EtOH). b. MCP 45359 (WC18.050497), male, 192 mm TL (body in lateral view, specimen fixed in formalin and preserved in EtOH). c. MCP 45359 (WC12.050497), female, 169 mm TL (body in lateral view, specimen fixed in formalin and preserved in EtOH); Brazil, rio Solimões-Japurá confluence, Amazonas dr. Note the sexual dimorphism in caudal filament height. Scale bars = 5 mm.
Fig. 2 in A taxonomic revision of the Neotropical electric fish genus Brachyhypopomus (Ostariophysi: Gymnotiformes: Hypopomidae), with descriptions of 15 new species
Fig. 2. Collection records for Brachyhypopomus based on 11,750 specimens from 2,642 georeferenced museum lots. Map of South and southern Central America based on HydroSHEDS data. Elevation data refers to altitude above mean sea level.
manuscript (atmosphere-3145955) titled: The Black Sea Upwelling System: Analysis on the Western Shallow Waters Authored by: Maria Emanuela Mihailov was accepted in Atmosphere (ISSN 2073-4433) on 15 August 2024
<p>Datasets represents the modelling results for:</p> <p>- Coastal Upwelling Transport Index (CUTI) of the National Oceanic and Administrative Administration’s Environmental Research Division (NOAA-ERD) was used to derive the time series of the coastal upwelling index in four locations on the north-western Black Sea coast. The coastal upwelling index time series was calculated using monthly average wind fields from the European Centre for Medium-Range Weather Forecasts (ECMWFs) reanalysis and MATLAB software to compute the CUTI </p> <p>- The upwelling index (UI) is computed using the CUTI Formula (<span>Bakun Index </span>), defined as CUTI (m3·s−1·100 m−1), representing the volume transport per distance unit of an alongshore section. The sign of Ekman transport is changed to define positive or negative values of UI as a response to upwelling or downwelling favourable winds.<br>To compute the BEUTI, Copernicus Marine Service [1] data are used for dedicated locations.</p> <p>[1] <span>Grégoire,<em> </em>M.;<em> </em>Vandenbulcke,<em> </em>L.;<em> </em>Capet,<em> </em>A.<em> </em>Black<em> </em>Sea<em> </em>Biogeochemical<em> </em>Reanalysis<em> </em>(CMEMS<em> </em>BS-Biogeochemistry)<em> </em>(Version<em> </em>1)<em> </em>set.<em> </em>Copernicus<em> </em>Monitoring<em> </em>Environment<em> </em>Marine<em> </em>Service<em> </em>(CMEMS).<em> </em>2020.<em> </em>Available<em> </em>online:<em> </em>https://marine.copernicus.eu/<em> </em>(accessed<em> </em>on<em> </em>10<em> </em>November<em> </em>2023).</span></p>
FIGURE 15 in An Early Neogene Elasmobranch fauna from the southern Caribbean (Western Venezuela)
FIGURE 15. Early Neogene chondrichthyan diversity in the Americas. Tropical America: Barbados (Ba), Brazil (Br), Colombia (Co), Costa Rica (Cs), Cuba (Cu), The Grenadines (Gr), Panamá (Pa), Perú (Pu), Trinidad (Tr) and Venezuela (Ve). North America: United States of America (US). Southern South America: Argentina (Ar) and Chile (Ch). Aquitanian (Anq), Burdigalian (Brd), Langhian (Lngh); early Miocene without differentiation (EM), early-Middle Miocene (E- MM). Formation(Fm.), early (E). Note: to references see "Paleodiversity significance" (see Discusion).
FIGURE 15 in A new megalosaurid theropod dinosaur from the late Middle Jurassic (Callovian) of north-western Germany: Implications for theropod evolution and faunal turnover in the Jurassic
FIGURE 15. Mid-caudal vertebra of Wiehenvenator albati in anterior (1) and lateral (2; stereophotographs) views. Abbreviations as in Figure 14, and: as, anterior spur. Scale bar equals 100 mm.
FIGURE 15 in New Anthribidae (Coleoptera: Curculionoidea) in Dominican and Mexican ambers
FIGURE 15. Holotype of Choragus exsertus sp. nov. PACO no. C-90 in Dominican amber. 1, dorsal view, scale bar equals 0.3 mm; 2, ventral view, scale bar equals 0.4 mm; and 3, lateral view, scale bar equals 0.4 mm.
FIGURE 15 in Pleistocene Bovidae (Mammalia) from Malapa, Gauteng Province, South Africa
FIGURE 15. Lingual view of Malapa UW 88-518 and UW 88-519 demonstrating high occlusal relief and sharp cusps.
FIGURE 15 in Bryozoan fauna from the Permian (Artinskian-Kungurian) Zhongba Formation of southwestern Tibet
FIGURE 15. Thin section photographs of Rhabdomeson sp. SMF 23.160 (1–4) and SMF 23.158 (5); and Primorella rotunda Gorjunova, 1985, SMF 23.163 (6) and SMF 23.162 (7–9). 1–3, branch oblique section; 4 and 5, longitudinal section; 6, tangential section; and 7–9, oblique section.
FIGURE 15 in Patterns of diversification and phylogenetic structure in the dorsolateral head musculature of Neotropical electric eels (Ostariophysi: Gymnotiformes), with a myological synonymy
FIGURE 15 | Lateral view of dorsolateral musculature of Microsternarchus cf. bilineatus (Hypopomidae), MBUCV-V 7298, 59.2 mm LEA. Anatomical abbreviations in Tab. 1. Scale bar = 1 mm.
FIGURE 15 in Late Messinian mollusks and vertebrates from Moncucco Torinese, north-western Italy. Paleoecological and paleoclimatological implications
FIGURE 15. Relative abundances of the glirid species within each glirid assemblage from Moncucco Torinese.
FIGURE 15 in Pleistocene cave hyenas in the Iberian Peninsula: New insights from Los Aprendices cave (Moncayo, Zaragoza
FIGURE 15. Palaeogeographic and diachronic distribution of the Crocuta in the Iberian Peninsula. The numbers refer to the sites listed in Appendix 7.
Fig. 15. A in Giant theropod dinosaurs from Asia and North America: Skulls of Tarbosaurus bataar and Tyrannosaurus rex compared
Fig. 15. A. Ventral view of the skull of Tarbosaurus bataar GIN 107/1 (A1) and explanatory drawing of the same (A2). B. Tyrannosaurus rex BHI−3033; lateral view of vomer (B1), lateral view of pterygoid (B2), dorsal view of pterygoid (B3). Not to scale.
Fig. 15. Asterocheres eurychelatus n in Copepods of the genus Asterocheres Boeck, 1859 (Siphonostomatoida: Asterocheridae) from Korean waters
Fig. 15. Asterocheres eurychelatus n. sp., female. A, maxilliped; B, leg 1; C, leg 2; D, endopod of leg 3; E, leg 4; F, exopod of leg 5; G, left side of genital double-somite, dorsal. Scale bars: 0.02 mm.
FIGURE 15 in Taxonomy and species diversity of Holocene pylonioid radiolarians from surface sediments of the northeastern Indian Ocean
FIGURE 15. Photographs of the encountered morphotypes of Pylodiscus spinulosus (Chen and Tan, 1989). All are Frview at Type 2. Scale bar equals 0.1 mm. All specimens are from YDY05-01.
FIGURE 15 in A new multi-faceted framework for deciphering diplodocid ontogeny
FIGURE 15. Selection of the diplodocid femoral dataset used throughout this ontogenetic analysis. Top row diplodocines, from left to right: CM 33991 (Diplodocus longus), CM 21788 (D. longus), CM 30762 (D. longus), MOR 790 7-5-97-7 (Diplodocus sp.), MOR 790 7-23-95-122 (Diplodocus sp.), MOR 592-35 (Diplodocus sp.), CM 21752 (Diplodocus sp.), SMA 0013 (Diplodocus sp.), CM 84 (D. carnegii); Bottom row apatosaurines, from left to right: AMNH 613 (Apatosaurus sp.), OMNH 1279 (Apatosaurus sp.), AMNH 606 (Apatosaurus sp.), MWC 5439 (Apatosaurus sp.), CM 21784 (A. louisae), CM 33997 (A. louisae), MOR 700 7-24-91-31 (Apatosaurus sp.), AMNH 353 (Apatosaurus sp.), SMA 0014 (Apatosaurus sp.), CM 85 (Apatosaurus sp.), MOR 857 7-16-92-30 (Apatosaurus sp.), MWC "Moffit Co. Apato." (Apatosaurus sp.). Scale bar equals 1 m. Note the colored line on CM 84 and MWC "Moffit Co. Apato." illustrate how femoral positions and trends were examined. Colored lines to the far right of each row indicate the general allometric changes of each femur scaled to the same length (Black line = femoral length). Diplodocus row: Yellow lines = MOR 790 7-5-97-7, Blue lines = MOR 592-35, Red lines = CM 84. Apatosaurus row: Green lines = AMNH 613, Yellow lines = CM 33997, Blue lines = MOR 700 7-24-91-31, Red lines = MWC "Moffit Co. Apato."
FIGURE 15 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 15. Two-dimensional plot Lsn (standardised length form apex to the protoconch) vs. AV (ventral aspect) of guards of Bln. kazimiroviensis from central and southern Russia and Central Asia, as illustrated by Naidin (1975). The dashed lines indicate the variability of Bln. kazimiroviensis and Bln. skolozdrownae from the Maastricht and the Middle Vistula valley regions.
FIGURE 15 in Mammals from the earliest Uintan (middle Eocene) Turtle Bluff Member, Bridger Formation, southwestern Wyoming, USA, Part 2: Apatotheria, Lipotyphla, Carnivoramorpha, Condylartha, Dinocerata, Perissodactyla and Artiodactyla
FIGURE 15. Merycobunodon? walshi new species from TBM. RM1 or 2 (UCM 67888, holotype, with 1 original specimen, 2-4 cast showing detail better) in occlusal (1- 2), posterior (3), and anterior (4) views. Scale bar equals 1 mm.
FIGURE 15. Schellwienella ornata Demanet, 1934 in New insights on Tournaisian-Visean (Carboniferous, Mississippian) athyridide, orthotetide, rhynchonellide, and strophomenide brachiopods from southern Belgium
FIGURE 15. Schellwienella ornata Demanet, 1934 from Visé, Visé Formation (Visean, Warnantian). 1-8, RBINS a5922 (lectotype), articulated internal mould in ventral, enlarged ventral (showing the extent of the traces left by the dissolved dental plates), dorsal, lateral, posterior, and anterior views, and internal views of a latex cast (SEM) showing the internal morphology of the posterior part of the specimen (7-8). 9-14, RBINS a5923 (paralectotype), articulated specimen (partly sectioned, probably by Demanet) in ventral, dorsal, lateral, posterior, and anterior views, and close-up (SEM) of the parvicostellate ornamentation in the central part of the dorsal valve. Scale bars equal 10 mm (1, 3-6, 9-13), 5 mm (2), 2.5 mm (7-8), 1.25 mm (14).
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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.