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Fig. 5 in Review of the Oriental stick insect genus Trachythorax Redtenbacher, 1908 with two new species from Vietnam and comments on egg parasitism and morphological counteradaptations (Phasmida, Lonchodidae, Necrosciinae)
Fig. 5. Trachythorax albomaculatus sp. nov., in culture. A, mating pair, dorsal view. B, mating pair, ventral view. C, mating pair, lateral view. D, ♂, dorsal view. E. ♂, lateral view. F, ♂, head and thorax, dorsolateral view. G, ♀, head and thorax, dorsolateral view. H, ♂, ventral view. I, newly hatched nymph, dorsal view. J, subadult ♂ nymph. K, ♀ nymph.
Fig. 4 in Review of the Oriental stick insect genus Trachythorax Redtenbacher, 1908 with two new species from Vietnam and comments on egg parasitism and morphological counteradaptations (Phasmida, Lonchodidae, Necrosciinae)
Fig. 4. Trachythorax albomaculatus sp. nov., paratype ♀ (RBINS). A, terminalia, dorsal view. B, terminalia, lateral view. C, terminalia, ventral view.
Fig. 2 in Review of the Oriental stick insect genus Trachythorax Redtenbacher, 1908 with two new species from Vietnam and comments on egg parasitism and morphological counteradaptations (Phasmida, Lonchodidae, Necrosciinae)
Fig. 2. Trachythorax albomaculatus sp. nov., holotype ♂ (RBINS). A, terminalia, dorsal view. B, terminalia, lateral view. C, terminalia, ventral view.
Fig. 7 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 7. Late Tremadocian conchoprimitid ostracod Conchoprimitia? iglesiasi sp. nov. Iglesias collection, from the Floresta Formation, Abra de Santa Laura section of the Cordillera Oriental Argentina. A. JUY−P 041, internal mould of right valve, lateral view. B. JUY−P 042, internal mould of left valve, lateral view. C. Holotype JUY−P 043, left valve in lateral view. D. JUY−P 044, left valve in lateral view. Scale bars 200 µm.
Fig. 6 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 6. Late Tremadocian ostracod Nanopsis coquena Salas, Vannier, and Williams, 2007 from the Cordillera Oriental Argentina. A, B, D–F. Humacha Member, middle levels of the Humacha section. A. CEGH−UNC 24015, left valve in lateral view. B. CEGH−UNC 24018, left valve in lateral view. C. Iglesias collection, Floresta Formation, Abra de Santa Laura section; JUY−P 045, internal mould of right valve, lateral view. D. CEGH−UNC 24021, right valve in lateral view. E. CEGH−UNC 24019, left valve in lateral view. F. CEGH−UNC 24023, right valve in lateral view. Scale bars 100 µm.
Fig. 4. Late Tremadocian soanellid ostracods from the Cordillera Oriental Argentina. A–C in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 4. Late Tremadocian soanellid ostracods from the Cordillera Oriental Argentina. A–C. Saltite erichseni (Harrington, 1938). San Bernardo Formation from Cerro San Bernardo section. A. CEGH−UNC 21150, internal mould of left valve, lateral view. B. CEGH−UNC 21149, internal mould of right valve, lateral view. C. CEGH−UNC 23994, external mould of right valve, lateral view. D–H. Saltite kuraq sp. nov. Humacha Member of Santa Rosita Formation from Humacha section. D. CEGH−UNC 24004, internal mould of left valve, lateral view. E. Holotype CEGH−UNC 23999, internal mould of left valve, lateral view. F. CEGH−UNC 24000, internal mould of left valve, lateral view. G. CEGH−UNC 24002, external mould of left valve, lateral view. H. CEGH−UNC 24005, external mould of right valve, lateral view. Scale bars 100 µm.
Fig. 3 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 3. Lithologic columns indicating ostracod−bearing levels (asterisks) of the studied sections. A. Abra de Santa Laura section. B. San Bernardo Formation (redrawn from Benedetto and Carrasco 2002). C. Pascha−Incamayo area, 1, western flank section; 2, eastern flank section (redrawn from Astini 2003). D. Quebrada de Humacha section (redrawn from Muñoz 2009). E. Quebrada Chalala (redrawn from Benedetto and Carrasco 2002).
Fig. 9 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 9. Palaeogeographic distribution of ostracods in the Late Tremadocian. The circle embraced the Gondwana and peri−Gondwana Tremadocian records of ostracods. Modified from Williams et al. (2008).
Fig 2 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig 2. Records of Tremadocian ostracods in the Northwest Argentinean Basin and in the rest of the world. Chronostratigraphic global units based on Bergström et al. (2009). Stratigraphic units, age, and ostracods records based on Hou 1953a, b; Schallreuter 1993; Williams and Siveter 1998; Ortega and Albanesi 2003; Waisfeld et al. 2006; Zeballo et al. 2003, 2008; Williams et al. 2008; Salas and Vaccari 2009; Egenhoff et al. 2010; Melnikova et al. 2010 and our own data.
Fig. 1 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 1. Geological setting and location of ostracod localities (asterisks): Abra de Santa Laura (A), Cerro San Bernardo in Sierra de Mojotoro (B), Pascha−Incamayo area (C), Quebrada de Humacha (D), and Purmamarca area (E). Modified after Salas et al. (2007).
Fig. 8 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 8. Late Tremadocian binodicopids ostracods from the Northwest Basin of Argentina. A–C, E. Orechina violetae sp. nov. Coquena Formation in Chalala section, Purmamarca area. A. Holotype CEGH−UNC 24029, right valve in lateral view. B. CEGH−UNC 24030, left valve in lateral view. C. CEGH−UNC 24031, right valve, lateral (C1) and ventral (C2) views. E. CEGH−UNC 24036, internal mould of right valve, lateral view. D, F–H. Orechina catalinae sp. nov. Humacha Member of the Santa Rosita Formation, lower part of the Humacha section. D. CEGH−UNC 24017, left valve in lateral view. F. CEGH−UNC 24027, left valve in lateral view. G. Holotype CEGH−UNC 24037, left valve in lateral view. H. CEGH−UNC 24028, right valve in lateral view. Scale bars 100 µm.
Fig. 5 in New insights into the early diversification of the Ostracoda: Tremadocian ostracods from the Cordillera Oriental, Argentina
Fig. 5. Late Tremadocian soanellid ostracod Saltite uchuy sp. nov. from the Parcha Formation in the Pascha−Incamayo area of Cordillera Oriental, Argentina. A. CEGH−UNC 24006, left valve in lateral view. B. Holotype CEGH−UNC 24007, left valve in lateral view. C. CEGH−UNC 24012, internal mould of right valve in lateral view. D. CEGH−UNC 24008, internal mould of left valve in lateral view. E. CEGH−UNC 24010, internal mould in dorsal view. F. CEGH−UNC 24011, internal mould in ventral view. G. CEGH−UNC 24013, internal mould of right valve, lateral view. Scale bars 100 µm.
Ultrafast photoresponse of vertically oriented TMD films probed in a vertical electrode configuration on Si chips
<p>This dataset contains the measurement data for figures published in the journal article: </p> <p> Ultrafast photoresponse of vertically oriented TMD films probed in a vertical electrode configuration on Si chips (https://doi.org/10.1039/D2NA00313A)</p> <p>by Topias Järvinen, Seyed-Hossein Hosseini Shokouh, Sami Sainio, Olli Pitkänen and Krisztian Kordas</p>
Fig. 4 in Scapular orientation in theropods and basal birds, and the origin of flapping flight
Fig. 4. Angles between furcular arms in non−avian theropods and birds. Data sources listed in Table 1.
Fig. 1 in Scapular orientation in theropods and basal birds, and the origin of flapping flight
Fig. 1. Scapular position and glenoid orientation in articulated skeletons of non−avian dinosaurs, with glenoids indicated by arrows. A. Dorsal view of the ornithischian dinosaur Psittacosaurus mongoliensis, AMNH 6254, showing lateral position and wide spacing of scapulae. B. Lateral view of the ornithischian dinosaur Centrosaurus apertus, AMNH 5351, showing ventral orientation of glenoid and position of glenoid anteroventral to ribcage. C. Lateral view of the ornithomimid theropod dinosaur Struthiomimus altus, AMNH 5339, showing position of glenoid anteroventral to ribcage. D. The deinonychosaurian theropod dinosaur Velociraptor mongoliensis, IGM 100/976, in dorsal (D1), right lateral (D2), and anterior (D3) views, with the furcula outlined in white for clarity, showing that the scapulae are widely spaced, laterally positioned, and exhibit ventrally oriented glenoids, as in other dinosaurs. Broken white lines in (D1) indicate lateral extemities of vertebral column.
Fig. 3 in Scapular orientation in theropods and basal birds, and the origin of flapping flight
Fig. 3. Articulated skeletons of Mesozoic birds, showing scapular position and glenoid orientation, with glenoids indicated by arrows. A. AMNH cast of "Berlin specimen" of Archaeopteryx lithographica, showing that the glenoids are anteroventral to the ribcage. The unnatural position of the left humerus above the glenoid is an artifact of dislocation of the left shoulder. B. AMNH cast of the "Eichstätt specimen" of Archaeopteryx lithographica, showing that the glenoid is anteroventral to the ribcage. C. Confuciusornis sanctus in dorsal view, showing wide spacing and lateral position of scapulae, with lateral extremities of vertebral column (extrapolated from dimensions of disarticulated dorsal vertebrae) represented by a pair of broken lines. Modified from Chiappe et al. (1999). D. The enantiornithine bird Eoalulavis hoyasi, LH 13500a, in dorsal view, showing close spacing and dorsal position of scapulae.
FIG. 16 in Taxonomic review of the potter wasp genus Antepipona de Saussure, 1855 (Hymenoptera, Vespidae, Eumeninae) from Vietnam, with descriptions of two new species and keys to the Oriental fauna
FIG. 16. — Characters of females of Antepipona de Saussure, 1855 (except a male of A. brunnipes (Fabricius, 1804) and A. minutissima Giordani Soika, 1982): A, A. excelsa Giordani Soika, 1982, SII, lateral view; B, D, I, L, A. sibilans (Cameron, 1903): SII, lateral view (B) pronotum dorsal view (D), clypeus, frontal view (I); metanotum, dorsal view (L); C, A. excelsa, pronotum, dorsal view; E, A. luzonensis (Rohwer, 1919), pronotum, dorsal view; F, A. minutissima, clypeus, frontal view; G, H, K, A. brunnipes: clypeus, frontal view, male (G); clypeus, frontal view (H); pronotal carina (K). Not to scale.
FIG. 3 in Taxonomic review of the potter wasp genus Antepipona de Saussure, 1855 (Hymenoptera, Vespidae, Eumeninae) from Vietnam, with descriptions of two new species and keys to the Oriental fauna
FIG. 3. — Antepipona bipustulata (de Saussure, 1855), from Vietnam: A, C, D, female; B, male: A, B, facial view; C, pronotum, frontal view; D, habitus, lateral view. Scale bar: 1 mm.
FIG. 6 in Taxonomic review of the potter wasp genus Antepipona de Saussure, 1855 (Hymenoptera, Vespidae, Eumeninae) from Vietnam, with descriptions of two new species and keys to the Oriental fauna
FIG. 6. — Antepipona ceylonica (de Saussure, 1867), genitalia: A, inner aspect of paramere with volsella and digitus; B, digitus; C, aedeagus, ventral view; D, aedeagus, lateral view. Scale bars: 1 mm.
FIG. 10 in Taxonomic review of the potter wasp genus Antepipona de Saussure, 1855 (Hymenoptera, Vespidae, Eumeninae) from Vietnam, with descriptions of two new species and keys to the Oriental fauna
FIG. 10. — Antepipona tytides (Cameron, 1904), genitalia: A, inner aspect of paramere with volsella and digitus; B, digitus; C, aedeagus, ventral view; D, aedeagus, lateral view. Scale bars: 1 mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.