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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. 1 in Vertebral fusion in two Early Jurassic sauropodomorph dinosaurs from the Lufeng Formation of Yunnan, China
Fig. 1. Location and stratigraphic context of the specimens. A. Location (dinosaur silhouette) of the Dalishu bonebed locality in Yunnan Province, China. B. Stratigraphic section of Lower Jurassic strata in the Lufeng Basin. Based on Xing et al. (2013).
Fig. 5. The 4 in Vertebral fusion in two Early Jurassic sauropodomorph dinosaurs from the Lufeng Formation of Yunnan, China
Fig. 5. The 4th and 5th caudal vertebrae of Sauropoda gen. et sp. indet. (ZLJ 0033) from Dalishu bonebed, Lower Jurassic, in right lateral (A), left lateral (B), dorsal (E), and ventral (F) views; anterior (C, G) and posterior (D, H) views of 4th and 5th caudal vertebrae, respectively. Red line in F shows location of the chevron articulation; red line in G shows boundary between proliferation and centrum.
Fig. 2. The 7 in Vertebral fusion in two Early Jurassic sauropodomorph dinosaurs from the Lufeng Formation of Yunnan, China
Fig. 2. The 7th and 8th cervical vertebrae of spondyloarthropathy dinosaur Lufengosaurus huenei Young, 1941 (ZLJ T001) from Dalishu bonebed, Lower Jurassic, in right lateral (A), left lateral (B), posterior (C), dorsal (D), ventral (E), and anterior (F) views.
Fig. 3 in Vertebral fusion in two Early Jurassic sauropodomorph dinosaurs from the Lufeng Formation of Yunnan, China
Fig. 3. Details of the rugose surfaces of the posterior neural-spine faces of the 7th (A) and 8th (B) cervical vertebra of spondyloarthropathy dinosaur Lufengosaurus huenei Young, 1941 (ZLJ T001) from Dalishu bonebed, Lower Jurassic.
Fig. 2 in Two Swallow Species from the Early Pliocene of Langebaanweg (South Africa)
Fig. 2. Fragmentary humeri of a medium−sized swallow species from the early Pliocene Varswater Formation at Langebaanweg, South Africa in cranial (A1, B1) and caudal (A2, B2) view. A. Left distal humerus SAM−PQ L 70289. B. Right distal humerus SAM−PQ L 70290. Abbreviation: pit, small depression on caudal surface of processus supracondylaris dorsalis.
Fig. 1 in Two Swallow Species from the Early Pliocene of Langebaanweg (South Africa)
Fig. 1. Fragmentary humeri of a large swallow species from the early Pliocene Varswater Formation at Langebaanweg, South Africa in cranial (A1, B1, C1) and caudal (A2, B2, C2) view. A. Left humerus SAM−PQ L 24915T. B. Right distal humerus SAM−PQ L 70288. C. Right distal humerus SAM−PQ L 70406. Abbreviations: cd, condylus dorsalis; ct, caudal tubercle; cv, condylus ventralis; fpd, fossa pneumotricipitalis dorsalis; fpv, fossa pneumotricipitalis ventralis; mps, attachment site for tendon of M. pronator superficialis; pf, processus flexorius; psd, processus supracondylaris dorsalis; sst, sulcus scapulotricipitalis.
Fig. 6. Two contrasting pterosaur phylogenies. A in The extent of the pterosaur flight membrane
Fig. 6. Two contrasting pterosaur phylogenies. A. Phylogeny from Lü et al. (2009). B. A simplified version of that presented by Wang et al. (2005). Thick black lines indicate species or groups of taxa for which the fossil evidence supports an ankle attachment of the wing.
Fig. 3 in Molecular phylogenetics and systematics of two enteric helminth parasites (Baylisascaris laevis and Diandrya vancouverensis) in the Vancouver Island marmot (Marmota vancouverensis)
Fig. 3. Bayesian consensus phylogram based on Baylisascaris and outgroup alignments of concatenated nuclear sequences (28S, ITS, and ard1) from GenBank and this study (B. laevis). Branch labels represent Bayesian posterior probabilities. Branch lengths are scaled to expected number of substitutions per site. Abbreviations refer to sampling sites (AK = Alaska, ID = Idaho, CT = Connecticut; IL = Illinois; CA = California; WV = West Virginia; ALB = Alberta). See also Table 1.
Fig. 2 in Molecular phylogenetics and systematics of two enteric helminth parasites (Baylisascaris laevis and Diandrya vancouverensis) in the Vancouver Island marmot (Marmota vancouverensis)
Fig. 2. Bayesian consensus phylogram based on Baylisascaris and outgroup alignments of concatenated mitochondrial sequences (12S, cox1, and cox2) from GenBank and this study (B. laevis). Branch labels represent Bayesian posterior probabilities. Branch lengths are scaled to expected number of substitutions per site. Abbreviations refer to sampling sites (AK = Alaska, ID = Idaho, CT = Connecticut; IL = Illinois; CA = California; WV = West Virginia; ALB = Alberta). See also Table 1.
Fig. 1 in Molecular phylogenetics and systematics of two enteric helminth parasites (Baylisascaris laevis and Diandrya vancouverensis) in the Vancouver Island marmot (Marmota vancouverensis)
Fig. 1. Known geographic distributions of Baylisascaris laevis and Diandrya composita in North America.
Fig. 4 in Molecular phylogenetics and systematics of two enteric helminth parasites (Baylisascaris laevis and Diandrya vancouverensis) in the Vancouver Island marmot (Marmota vancouverensis)
Fig. 4. Bayesian consensus phylogram based on Baylisascaris and outgroup alignments of concatenated mitochondrial (12S, cox1, and cox2) and nuclear sequences (28S, ITS, and ard1) from GenBank and this study (B. laevis). Branch labels represent Bayesian posterior probabilities. Branch lengths are scaled to expected number of substitutions per site. Abbreviations refer to sampling sites (AK = Alaska, ID = Idaho, CT = Connecticut; IL = Illinois; CA = California; WV = West Virginia; ALB = Alberta). See also Table 1.
Fig. 4 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 4. Haptor of Polystomoides brasiliensis showing the deep incisions between suckers. Scale bar = 200 μm.
Fig. 3 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 3. Violin plot of the genital spines number. A = Aussietrema infecting pleurodires; B = Neopolystoma infecting pleurodires; C = Polystomoides infecting pleurodires; D = Uropolystomoides infecting pleurodires of the Australian Realm; E = Uropolystomoides infecting pleurodires of the Ethiopian Realm; F = Fornixtrema infecting cryptodires; G = Neopolystoma infecting cryptodires; G = Polystomoides infecting cryptodires; I = Uropolystomoides infecting cryptodires; J = Apalonotrema moleri infecting a cryptodire host. K = Uteropolystomoides nelsoni infecting a cryptodire host.
Fig. 1 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 1. Lateroventral vaginae as observed for Neopolystoma kreffti (A), Uropolystomoides scottae (B) and Polystomoides brasiliensis (C). Annotations: gb, genital bulb; ov, ovary; te, testis; vg, vaginae. Scale bar = 200 μm.
Fig. 6 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 6. Hamuli of Polystomoides spp. A = Polystomoides japonicum Ozaki, 1935; B = Polystomoides magdalenensis Lenis and Garcia-Prieto, 2009; C = Polystomoides ocellatum (Rudolphi, 1819); D = Polystomoides pauli (Timmers and Lewis, 1979); E = Polystomoides platynotae Combes and Rohde, 1979; F = Polystomoides rohdei; G = Polystomoides brasiliensis; H = Polystomoides fuquesi Man´e-Garzon and Gil, 1962; I = Polystomoides uruguayensis Man´e-Garzon and Gil, 1961. Scale bar = 50 μm.
Fig. 2 in Classification of pleurodire polystomes (Platyhelminthes, Monogenea, Polystomatidae) revisited with the description of two new genera from the Australian and Neotropical Realms
Fig. 2. Violin plot of inter-vaginal distance as % of the body width at the level of the vagina. The plot visualises the probability density of the data at different values. Within each violin is a marker for the median of the data as well as marker indicating the interquartile range. A = Aussietrema infecting pleurodires; B = Neopolystoma infecting pleurodires; C = Polystomoides infecting pleurodires; D = Uropolystomoides infecting pleurodires of the Australian Realm; E = Uropolystomoides infecting pleurodires of the Ethiopian Realm; F = Fornixtrema infecting cryptodires; G = Neopolystoma infecting cryptodires; G = Polystomoides infecting cryptodires; I = Uropolystomoides infecting cryptodires; J = Apalonotrema moleri infecting a cryptodire host. K = Uteropolystomoides nelsoni infecting a cryptodire host.
Fig. 3 in Morphological and molecular studies on two myxosporean infections of cyprinid fishes: Thelohanellus pyriformis from tench and Thelohanellus cf. fuhrmanni from nase
Fig. 3. Spores of Thelohanellus cf. fuhrmanni. a) Schematic drawing of a spore in frontal view, b) Schematic drawing of a spore in sutural view, c) Microscopic photos of spores in frontal view. A spore in sutural view (inset).
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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.