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Fig. 2 in Differential patterns of definitive host use by two fish acanthocephalans occurring in sympatry: Pomphorhynchus laevis and Pomphorhynchus tereticollis
Fig. 2. Relationship between fish biomass (g.100m-2) and P. laevis (a) or P. tereticollis (b) mean abundance per fish species, across fish species and localities (Ouche and Vingeanne localities). Both variables were log10-transformed.
Fig. 9. Smenospongia duokyeo n in Twelve new species of two genera Smenospongia and Cacospongia (Demospongia: Dictyoceratida: Thorectidae) from Korea
Fig. 9. Smenospongia duokyeo n. sp. A, entire animal; B, closed surface; C and E, surface skeletal structure; D, choanosome skeletal structure; F, closed primary fibres. Scale bars: A = 2 cm, C-E = 200 μm, F = 100 μm.
Fig. 11. Cacospongia bakusi n in Twelve new species of two genera Smenospongia and Cacospongia (Demospongia: Dictyoceratida: Thorectidae) from Korea
Fig. 11. Cacospongia bakusi n. sp. A, entire animal; B, closed surface; C, surface skeletal structure; D, choanosome skeletal structure; E, F, closed primary fibres. Scale bars: A = 2 cm, C, D = 200 μm, E, F = 100 μm.
Fig. 8. Smenospongia varispina n in Twelve new species of two genera Smenospongia and Cacospongia (Demospongia: Dictyoceratida: Thorectidae) from Korea
Fig. 8. Smenospongia varispina n. sp. A, entire animal; B, closed surface; C, surface skeletal structure; D, choanosome skeletal structure; E, F, closed skeletal structure. Scale bars: A = 2 cm, C, D = 200 μm, E, F = 100 μm.
Fig. 4 in Differential patterns of definitive host use by two fish acanthocephalans occurring in sympatry: Pomphorhynchus laevis and Pomphorhynchus tereticollis
Fig. 4. Relationship between the phylo-structural index of specificity towards definitive hosts and observed prevalence in gammarid intermediate hosts (%) in P. laevis and P. tereticollis. The phylo-structural index of specificity increases with the taxonomic diversity of fish species used.
Fig. 4. Smenospongia arbuscula n in Twelve new species of two genera Smenospongia and Cacospongia (Demospongia: Dictyoceratida: Thorectidae) from Korea
Fig. 4. Smenospongia arbuscula n. sp. A, entire animal; B, closed surface; C, surface primary and secondary fibres; D, choanosome primary fibres; E, primary fibres enclosed egg ball; F, free egg ball. Scale bars: A = 2 cm, C, D = 200 μm, E = 50 μm, F = 10 μm.
Fig. 3. Smenospongia flavia n in Twelve new species of two genera Smenospongia and Cacospongia (Demospongia: Dictyoceratida: Thorectidae) from Korea
Fig. 3. Smenospongia flavia n. sp. A, entire animal; B, closed surface; C, surface skeletal structure; D, choanosome skeletal structure; E, closed primary fibre; F, skeletal structure. Scale bars: A = 2 cm, C, D = 200 μm, E = 100 μm, F = 200 μm.
Fig. 7. Smenospongia wiedenmayeri n in Twelve new species of two genera Smenospongia and Cacospongia (Demospongia: Dictyoceratida: Thorectidae) from Korea
Fig. 7. Smenospongia wiedenmayeri n. sp. A, entire animal; B, closed surface; C, surface secondary fibres; D, E, choanosomes skeletal structure; F, closed primary fibres. Scale bars: A = 3 cm, C-E = 200 μm, F = 100 μm.
Fig. 5 in First record of viviparity in polystomatid flatworms (Monogenea: Polystomatidae) with the description of two new species of Madapolystoma from the Madagascan anuran hosts Blommersia domerguei and Mantella expectata
Fig. 5. Scatter diagram of a × c plotted against b × c for all known Madapolystoma spp., M. magnahami n. sp. and M. isaloensis n. sp. The ellipses represent 95% of the confidence interval about the mean.
Fig. 4. a–b in First record of viviparity in polystomatid flatworms (Monogenea: Polystomatidae) with the description of two new species of Madapolystoma from the Madagascan anuran hosts Blommersia domerguei and Mantella expectata
Fig. 4. a–b) Ventral view of M. isaloensis n. sp. holotype. (c) Hamuli from mature specimens and (d) Marginal hooklets 1–8. Scale bars: B, 200 μm; C, 100 μm; D, 20 μm. Abbreviations: de, developing embryo; ee, early embryo; ev, excretory vessel; gb, genital bulb; gc, genito-intestinal canal; ha, hamuli. hp, haptor; ic, intestinal caecum; mh, marginal hooklet; mo, mouth; ph, pharynx; su, sucker; sv, seminal vesicle; va, vagina; vd, vas deferens; vi, vitelline follicles; vv, vitelline duct.
Fig. 3. a–b in First record of viviparity in polystomatid flatworms (Monogenea: Polystomatidae) with the description of two new species of Madapolystoma from the Madagascan anuran hosts Blommersia domerguei and Mantella expectata
Fig. 3. a–b) Ventral view of M. magnahami n. sp. holotype. (c) Hamuli from mature specimens and (d) Marginal hooklets 1 (top) and 2–8 (bottom). Scale bars: B, 500 μm; C, 100 μm; D, 25 μm. Abbreviations: em, embryo; ev, excretory vessel; gb, genital bulb; gc, genito-intestinal canal; ha, hamuli. hp, haptor; ic, intestinal caecum; mh, marginal hooklet; mo, mouth; pe, potential embryo; ph, pharynx; su, sucker; sv, seminal vesicle; va, vagina; vd, vas deferens; vi, vitelline follicles; vv, vitelline duct.
Fig. 2 in First record of viviparity in polystomatid flatworms (Monogenea: Polystomatidae) with the description of two new species of Madapolystoma from the Madagascan anuran hosts Blommersia domerguei and Mantella expectata
Fig. 2. Minimum Evolution tree for Madapolystoma spp. Numbers on nodes indicate bootstrap support values. Madapolystoma sp. from B. domerguei refers to M. magnahami n. sp. and Madapolystoma sp. from M. expectata refers to M. isaloensis n. sp.
Fig. 1. a in First record of viviparity in polystomatid flatworms (Monogenea: Polystomatidae) with the description of two new species of Madapolystoma from the Madagascan anuran hosts Blommersia domerguei and Mantella expectata
Fig. 1. a) Map of Madagascar with the distribution areas and sampling localities of the two investigated frogs; b) Blommersia domerguei; c) Mantella expectata. (Map-Library, 2007).
Fig. 6 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 6. Histopathologic sections of ceca which were obtained from dead chicks infected with Eimeria spp. Arrowhead indicates macrogametocytes with a prominent wall-forming body (A), and arrows indicate zygotes or early oocysts, which are surrounded by an oocyst wall (A and B). Pathological lesions could not be observed because of severe degradation after death. Scale bars indicate 20 μm.
Fig. 3 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 3. Phylogram of E. uekii, type B, other Eimeria spp., and related parasites (Cyclospora spp.) inferred by the neighbor-joining method using partial 18S rRNA gene sequences. Accession numbers and derived hosts are shown in parentheses. Scale bar represents substitutions per nucleotide, and bootstrap values are indicated (> 1000). Cystoisospora spp. are used as an outgroup taxon.
Fig. 4 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 4. Phylogram of E. uekii, type B, and other related Eimeria spp. inferred by the neighbor-joining method using partial mitochondrial cytochrome c oxidase subunit I gene sequences. Accession numbers and derived hosts are shown in parentheses. Scale bar represents substitutions per nucleotide, and bootstrap values are indicated (> 1000). Toxoplasma gondii is used as an outgroup taxon.
Fig. 2 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 2. Eimeria oocysts detected in the feces of Japanese rock ptarmigans. (A) E. uekii and (B) type B. Scale bars indicate 10 μm.
Fig. 1 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 1. Location of three sampled areas in Japan, Mt. Tateyama (36̊35′N, 137̊36′E), Norikuradake (36̊6′N, 137̊33′E), and Kitadake (35̊40′N, 138̊14′E) (triangle boxes 1–3).
Fig. 5 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica
Fig. 5. Composite line drawing of oocyst of Eimeria raichoi n. sp (previously referred as type B). Scale bars indicate 10 μm.
Figs 16-17 in On two Oxypodinus species from Madagascar, inhabitants of Impatiens inflorescences (Coleoptera: Staphylinidae, Aleocharinae)
Figs 16-17: (16) Oxypodinus levasseuri in inflorescence of Impatiens vilersii (photo by A. Erpenbach); (17) records of O. floricola (filled circle) and O. levasseuri (open circle) in Madagascar.
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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.