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Fig. 1 in New records of non-native ants (Hymenoptera: Formicidae) in four African countries
Fig. 1. Nylanderia bourbonica (Forel, 1886). A, head in full face view; B, habitus in lateral view. © Erin Prado, CASENT0188533, Antweb.org.
Fig. 7 in New records of non-native ants (Hymenoptera: Formicidae) in four African countries
Fig. 7. Trichomyrmex mayri (Forel, 1902). A, head in full face view; B, habitus in lateral view. © Michele Esposito, CASENT0919809, Antweb.org.
Fig. 7. A in The first record of the genus Olcinia Stål, 1877 from Cambodia and Vietnam with the description of two new species (Orthoptera: Tettigoniidae: Pseudophyllinae: Cymatomerini)
Fig. 7. A. Distribution map of Olcinia nuichuana sp. nov. and O. constanti sp. nov. B, O. constanti sp. nov. habitat in Kirirom N. P. (Photograph J. Constant May 2015). C, O. nuichuana sp. nov. habitat in Nui Chua N. P. (Photograph J. Constant July 2014).
Fig. 6 in The first record of the genus Olcinia Stål, 1877 from Cambodia and Vietnam with the description of two new species (Orthoptera: Tettigoniidae: Pseudophyllinae: Cymatomerini)
Fig. 6. Olcinia nuichuana sp. nov., holotype ♀. A, fore leg, lateral view. B, mid leg, lateral view. C, hind leg, lateral view. D, ovipositor, lateral view. E, subgenital plate (paratype), ventral view.
Fig. 2 in The first record of the genus Olcinia Stål, 1877 from Cambodia and Vietnam with the description of two new species (Orthoptera: Tettigoniidae: Pseudophyllinae: Cymatomerini)
Fig. 2. Olcinia constanti sp. nov., holotype ♀. right tegmen and corresponding alae. A, tegmen. B, ala. C, ala distal part. ppa, plica prima anterior. Sc+R, subcosta and radius.
Fig. 4 in The first record of the genus Olcinia Stål, 1877 from Cambodia and Vietnam with the description of two new species (Orthoptera: Tettigoniidae: Pseudophyllinae: Cymatomerini)
Fig. 4. Olcinia nuichuana sp. nov., holotype ♀. A, habitus, dorsal view. B, habitus, ventral view. C, habitus, lateral view. D, head and thorax, dorsal view. E, head and thorax, lateral view. F, forehead. G, meso- and metasternum ventral view. D–G not to scale.
Fig. 1 in The first record of the genus Olcinia Stål, 1877 from Cambodia and Vietnam with the description of two new species (Orthoptera: Tettigoniidae: Pseudophyllinae: Cymatomerini)
Fig. 1. Olcinia constanti sp. nov., holotype ♀. A, habitus, dorsal view. B, habitus, ventral view. C, habitus, lateral view. D, head and thorax, dorsal view. E, head and thorax, lateral view. F, forehead. G, meso- and metasternum, ventral view. D–G not to scale.
Fig. 3 in The first record of the genus Olcinia Stål, 1877 from Cambodia and Vietnam with the description of two new species (Orthoptera: Tettigoniidae: Pseudophyllinae: Cymatomerini)
Fig. 3. Olcinia constanti sp. nov., holotype ♀. A, fore leg, lateral view. B, mid leg, lateral view. C, hind leg, lateral view. D, ovipositor, lateral view. E, subgenital plate, ventral view.
Fig. 4 in The early fossil record of dinosaurs in North America: A new neotheropod from the base of the Upper Triassic Dockum Group of Texas
Fig. 4. Partial left maxilla of an archosaur (TMM 41936-1.1), Otis Chalk area, Dockum Group, Late Triassic, found with and possibly referable to neotheropod Lepidus praecisio gen. et sp. nov., in lateral (A), ventral (B), and medial (C) views, arrows indicate anterior direction. D. A replacement tooth in labial view within the fourth alveolus in anterolateral view (D 2), close up (D ).
Fig. 3 in The early fossil record of dinosaurs in North America: A new neotheropod from the base of the Upper Triassic Dockum Group of Texas
Fig. 3. The referred left femur of neotheropod Lepidus praecisio gen. et sp. nov., Otis Chalk area, Dockum Group, Late Triassic (TMM 41936-1.3) in anterior (A) and posterior (B) views and the bone tissues of the femur (D) through the entire cortex on the anterolateral side (C) and the middle and outer cortex on the posterolateral side (D). Arrows indicate the direction of the external surface of the femur.
Fig. 5 in The early fossil record of dinosaurs in North America: A new neotheropod from the base of the Upper Triassic Dockum Group of Texas
Fig. 5. Phylogenetic relationships of early theropod dinosaurs recovered here highlighting the phylogenetic position of Lepidus praecisio gen. et sp. nov. with the holotype only (A), simplified strict consensus of six MPTs, TL = 1058, CI = 0.5311, RI = 0.8250) or with all of the hypothesized material (B), simplified strict consensus of 18 MPTs, TL = 1061, CI = 0.5383, RI = 0.8303). The original taxon list and relationships outside of Dinosauria and within Ornithischia are exactly the same as that of Nesbitt et al. (2009b).
Fig. 1 in The early fossil record of dinosaurs in North America: A new neotheropod from the base of the Upper Triassic Dockum Group of Texas
Fig. 1. Map of the type locality of Lepidus praecisio gen. et sp. nov. near Signal Peak, southeast of Big Spring, Texas. The dotted circle is the approximate area that holotype came from and its relationship to the famous Otis Chalk localities.
Fig. 2 in The early fossil record of dinosaurs in North America: A new neotheropod from the base of the Upper Triassic Dockum Group of Texas
Fig. 2. Comparisons of almost naturally articulated ankle complexes of neotheropods. A. Lepidus praecisio gen. et sp. nov., Otis Chalk area, Dockum Group, Late Triassic (TMM 41936-1.3). B. Camposaurus arizonensis Hunt, Lucas, Heckert, Sullivan, and Lockley, 1998, Placerias Quarry, Chinle Formation, Late Triassic UCMP 34498), reversed. C. Coelophysis bauri Cope, 1887, Coelophysis Quarry, Chinle Formation, Late Triassic (AMNH FARB 30615). D. Zupaysaurus rougieri Arcucci and Coria, 2003, Colorados Formation, Late Triassic (PULR 076), reversed. Left (A, C) and right (B, D) tibia, fibula, and astragalocalcaneum in anterior (A 1–D1), medial (A2–D2), posterior (A3–D3), lateral (A4–D4), and ventral (A5–D5) views, arrows indicate anterior direction.
Fig. 4 in The weathering-modified iridium record of a new Cretaceous-Palaeogene site at Lechówka near Chełm, SE Poland, and its palaeobiologic implications
Fig. 4. Two−step interpretation of weathering−modified iridium anomaly in the K–Pg succession at Lechówka (see Fig. 3), showing a significant original iridium anomaly (A) altered by secondary redistribution/participation processes (B), resulting in a substantial extension of the iridium enrichment and a lower position of the diminished iridium spike relative to the K–Pg boundary clay, perhaps controlled by a precipitation front at an assumed redox barrier (cf. Sawłowicz 1993; Gawrilov 2010). Observed and expected weathering−controlled iridium chemostratigraphic profiles are shown (the iridiumr baseline is carefully taken as 0.1 ppb; see Table 2), as well as the comparative placement of the recognised iridium enrichment against a diversity of K–Pg reference levels and key localities (compiled from Crocket et al. 1988, Hansen et al. 1989, Koeberl et al. 2007, and Schulte et al. 2010).
Fig. 1 in The weathering-modified iridium record of a new Cretaceous-Palaeogene site at Lechówka near Chełm, SE Poland, and its palaeobiologic implications
Fig. 1. Location of the Lechówka section in Poland (A), and general view of this outcrop (B). K, Cretaceous; Pg, Palaeogene.
Fig. 2 in The weathering-modified iridium record of a new Cretaceous-Palaeogene site at Lechówka near Chełm, SE Poland, and its palaeobiologic implications
Fig. 2. Lithologic column, field photo and two close−ups of the K–Pg passage at Lechówka. Note a local abundance of burrows (b) and Fe oxy−hydroxides, especially in the boundary clay.
Fig. 2 in Genetic characterisation of Tanqua (von Linstow, 1879) (Nematoda: Gnathostomatidae) larval forms including new host and locality records
Fig. 2. Larval nematodes identified as Tanqua sp. 2A specimen 674-1 anterior tip (20x); 2B specimen 678-1 showing tooth like projections of pseudolabia (tl) and lateral pseudolabium (lp) (40x); 2C specimen 674-1 posterior trunk (4x) showing annulations (an). and 2D specimen 678-9 tail (20x) respectively showing annulations (an) and anus (as). The circled area in Fig. 2A is indicative of the damage to internal structures which precluded detailed morphological examination.
Fig. 1 in Genetic characterisation of Tanqua (von Linstow, 1879) (Nematoda: Gnathostomatidae) larval forms including new host and locality records
Fig. 1. Phylogenetic tree (of 18S sequences of nematodes) inferred using the Maximum Likelihood Method. The bootstrap values higher than 80 are indicated next to the branches. The new sequences generated from this study are indicated with asterisks.
Fig. 1 in Eyeworms of wild birds and new record of Thelazia (Thelaziella) aquilina (Nematoda: Spirurida)
Fig. 1. Thelazia (Thelaziella) aquilina on the cornea of an adult female Harpia harpyja in Amazonia region (Brazil).
Fig. 3 in Eyeworms of wild birds and new record of Thelazia (Thelaziella) aquilina (Nematoda: Spirurida)
Fig. 3. Morphology of Thelazia (Thelaziella) aquilina male: a) Posterior end, male, lateral view, spicules; b) Posterior end, right spicule and distal portion of the left spicule; c) Right spicule and gubernaculum (arrowhead); Distal portion of the right spicule, bulbar expansion with transparent hyaline membrane (arrows); d) Posterior end, male, ventral view, spicules and papillae pre (arrowhead) and post-cloacal (arrows).
ScienceDex guides
Understand access before you commit
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.