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Figs. 1 - 17 in The status of Lestes apollinaris Navas and L. henshawi Calvert
Figs. 1 - 17: morphological details. Figs. 1, 4, 5, 8, 11, 14, 16: Lestes apollinaris. Figs. 2, 6, 9, 12, 15, 17: L. tenuatus. Figs. 3, 7, 10, 13: L. henshawi. Figs. 1 - 3: color pattern of pterothorax; Figs. 4 - 7: male terminalia, dorsal view, Fig. 4 is Navas's original. Figs. 8-10: left cercus, dorsal view. Figs. 1 1 -1 3: hind lobe of male prothorax, dorsal view. Figs. 14 - 15: same, female. Figs. 16 - 17: female abdomen tip, lateral view
Fig. 1 in Resolving the Ophioderma longicauda (Echinodermata: Ophiuroidea) cryptic species complex: five sisters, three of them new
Fig. 1. Phylogenetic relationships and distribution of species of Ophioderma Müller & Troschel, 1840 in the Northeast and Tropical Atlantic Ocean and the Mediterranean Sea. A. Simplified phylogenetic relationships among species of Ophioderma described in this study, modified from Weber et al. (2019). Summary of reproductive strategy: S = broadcast spawner; B = brooder. Correspondence between species names, nuclear genetic clusters and COI mitochondrial lineages is summarized from Boissin et al. (2011) and Weber et al. (2019). C6 is tentatively assigned to O. zibrowii sp. nov. because it occurs far from the type locality and brooding species are expected to have low dispersal rates, leading to low gene flow between populations. B. Distribution of species of Ophioderma in the Northeast and Tropical Atlantic Ocean. C. Distribution of species of Ophioderma in the Mediterranean Sea.
FIG. 10 in On the taxonomic position of Phaenomenella Fraussen & Hadorn, 2006 (Neogastropoda, Buccinoidea) with description of two new species
FIG. 10. — Anatomy of Siphonalia cassidariaeformis (Reeve, 1846): A, B; ventral (A) and dorsal (B) views of body of specimen no. 1, removed from the shell; C, cephalopodium of no. 2, front view; D, penis of no. 3; E, F, foregut of no. 1, with right salivary gland in original position (E) and removed (F); G, stomach of no. 2, external view; H, stomach of no. 1, opened dorsally; I, stomach of no. 2, opened dorsally. Abbreviations: see material and methods. Scale bars: A-F, 10 mm; G, I, 5 mm; H, 1 mm
FIG. 8 in On the taxonomic position of Phaenomenella Fraussen & Hadorn, 2006 (Neogastropoda, Buccinoidea) with description of two new species
FIG. 8. — Anatomy of Phaenomenella nicoi n. sp.: A-D, MNHN-IM-2013-61636, male; E-G, MNHN-IM-2013-61637, female: A, soft body removed from the shell; B, penis; C, proboscis, opened dorsally; D, foregut, right lateral view; E, foregut, right lateral view, right salivary gland displaced; F, foregut, right lateral view, right salivary gland in original position; G, stomach, outer view. Abbreviations: see material and methods. Scale bars: 5 mm.
FIG. 4 in On the taxonomic position of Phaenomenella Fraussen & Hadorn, 2006 (Neogastropoda, Buccinoidea) with description of two new species
FIG. 4. — Shells of Phaenomenella samadiae n. sp.: A-C, holotype, MNHN-IM-2013-61617, SL 58.2 mm; D, ZHONGSHA 2015, st. CP4157, non-sequenced spm, MNHN-IM-2013-59393, SL 47.2 mm; E, F, ZHONGSHA 2015, st. CP4134, sequenced spm, MNHN-IM-2013-61674, SL 51.4 mm; G, ZHONGSHA 2015, st. CP4157, non-sequenced spm, MNHN-IM-2013-59665, SL 37.1 mm. Scale bar: 5 cm.
FIG. 2 in On the taxonomic position of Phaenomenella Fraussen & Hadorn, 2006 (Neogastropoda, Buccinoidea) with description of two new species
FIG. 2. — Phylogenetic tree of a dataset of Buccinoidea Rafinesque, 1815 obtained with Bayesian analysis of 28S gene sequences. Support values shown for the supported nodes with posterior probability values between 0.70 and 1.00 only.
Fig. 4 in A new species of Characidium (Characiformes: Crenuchidae) from coastal basins in the Atlantic Rainforest of eastern Brazil, with phylogenetic and phylogeographic insights into the Characidium alipioi species group
Fig. 4. Fast flowing stream, type locality of Characidium cricarense, at Cachoeira do Inferno rapids in rio Cricaré, São Mateus, ES, Brazil. GPS coordinates: 18°42'24.5"S 40°16'7.2"W.
FIG. 1 in On the taxonomic position of Phaenomenella Fraussen & Hadorn, 2006 (Neogastropoda, Buccinoidea) with description of two new species
FIG. 1. — Phylogenetic tree of a dataset of Buccinoidea Rafinesque, 1815 obtained with Bayesian analysis of COI gene sequences. Support values shown for the supported nodes with posterior probability values between 0.70 and 1.00 only. The numbers in brackets following the species names correspond to illustrated specimens at the bottom of the figure.
FIG. 11 in On the taxonomic position of Phaenomenella Fraussen & Hadorn, 2006 (Neogastropoda, Buccinoidea) with description of two new species
FIG. 11. — Radulae of Siphonalia spp. A, S. cassidariaeformis (Reeve, 1846) no. 1; B, S. cassidariaeformis no. 2; C, S. pfefferi G. B. Sowerby III, 1900 no. 1;
Fig. 5 in A new species of Astyanax (Characiformes: Characidae) from the rio de Contas basin, Bahia, Brazil
Fig. 5. Collecting sites of Astyanax varii: (a) type locality, Brazil, Bahia State, Ubaitaba, Fazenda Progresso, rio Coricó, lower rio de Contas basin; (b) Brazil, Bahia State, Jussiape, Caraguataí, rio Água Suja at Balneário Rio da Barra, upper rio de Contas basin.
Fig. 2 in Movement and longitudinal distribution of a migratory fish (Salminus brasiliensis) in a small reservoir in southern Brazil
Fig. 2. Total time spent by dourados (Salminus brasiliensis) in the reservoir (Tin), total time spent in an unknown location (Tun) and total time spent outside of the reservoir in a stretch of the upstream Erechim river (Tout). ANOVA with permutation tested for differences among groups (F(2,54) = 87.17; p <0.0002). The numbers above the plots represent the number of individuals. Different letters above the plots represent significant differences according to Tukey's test. Circles represent outlier values; the heavy horizontal line crossing the box is the median; the bottom and top of the box are the lower and upper quartiles, respectively; and the whiskers are the minimum and maximum values.
Fig. 2. a in Revalidation and redescription of Steindachnerina nigrotaenia and redescription of S. insculpta (Characiformes: Curimatidae)
Fig. 2. a. Steindachnerina nigrotaenia, lectotype of Curimatus nigrotaenia, BMNH 1902.2.10.30, 43.5 mm SL, Brazil, Mato Grosso, rio Coxipó, upper rio Paraguai; b. LBP 1477, 43.4 mm SL, Brazil, Mato Grosso do Sul, Coxim, rio Taquari, upper rio Paraguai.
Fig. 1 in A new species of Astyanax (Characiformes: Characidae) from the rio de Contas basin, Bahia, Brazil
Fig. 1. Astyanax varii, Brazil, Bahia State: (a) MZUSP 121062, holotype, 41.4 mm SL, Ubaitaba, lower rio de Contas basin, rio Coricó; (b) live paratype, not catalogued.
Fig. 3 in Species or population? Systematic status of Vieja coatlicue (Teleostei: Cichlidae)
Fig. 3. Haplotype network recovered from analysis of the cyt b dataset for populations of Vieja coatlicue (Atlantic) and Vieja zonata (Pacific). Dashes lines represent mutational steps.
Fig. 2 in Species or population? Systematic status of Vieja coatlicue (Teleostei: Cichlidae)
Fig. 2. Bayesian phylogeny based on cytochrome b sequence data. Number above clades is posterior probability.
Fig. 3 in A new species of Astyanax (Characiformes: Characidae) from the rio de Contas basin, Bahia, Brazil
Fig. 3. Upper and lower jaws of Astyanax varii, UFBA 8405, paratype, 35.1 mm SL, lateral view, left side.
Fig. 1 in Species or population? Systematic status of Vieja coatlicue (Teleostei: Cichlidae)
Fig. 1. Map of Mexico displaying localities for specimens (triangles) examined and tissue samples (circles) for Vieja coatlicue (green) and Vieja zonata (black) used in this study. Star indicates locality for Vieja guttulata sample.
Fig. 6 in A new species of Paralithoxus (Siluriformes: Loricariidae: Ancistrini) from the highlands of Serra da Mocidade, Roraima State, Brazilian Amazon
Fig. 6. Type-locality of Paralithoxus mocidade in Ajarani River, tributary of the Branco River basin, located immediately downstream of a large waterfall. Photo by Marcos Amend.
Fig. 1 in A new species of Paralithoxus (Siluriformes: Loricariidae: Ancistrini) from the highlands of Serra da Mocidade, Roraima State, Brazilian Amazon
Fig. 1. Paralithoxus mocidade, holotype, INPA 54745, female, 50.5 mm SL, in lateral, dorsal and ventral views.
Fig. 5 in A new species of whiptail armored catfish, genus Pseudohemiodon (Siluriformes: Loricariidae) from the Orinoco River basin, Llanos region of Colombia and Venezuela
Fig. 5. Map of northern South America (Colombia and Venezuela) showing capture localities of Pseudohemiodon unillano, red star is type locality, some symbols may represents more than one lot.
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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.