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FIG. 1 in Two fossil conifer species from the Neogene of Alonissos Island (Iliodroma, Greece)
FIG. 1. — Geological sketch – map of Alonissos Island, by Jacobshagen & Matarangas (2004) (based on the work of Kelepertsis [1975] for the Institute of Geology and Mineral Exploration [I.G.M.E.]), modified. The Neogene formations are included by the red circles.
Fig. 1 in Descriptions of two new Vietomartyria species (Lepidoptera, Micropterigidae) from China
Fig. 1. Adults and habitat of Vietomartyria spp. A. Vietomartyria wuyunjiena sp. nov., holotype, ♂. B. Vietomartyria maoershana sp. nov., holotype, ♂. C. One adult of V. wuyunjiena sp. nov. perching on fern. D. Habitat of V. wuyunjiena sp. nov. E. Specimen collection of V. wuyunjiena sp. nov. by sweep net. F. One adult of V. wuyunjiena sp. nov. perching on the white curtain of a light trap.
Fig. 4 in Descriptions of two new Vietomartyria species (Lepidoptera, Micropterigidae) from China
Fig. 4. Male genitalia of Vietomartyria maoershana sp. nov. A. Dorsal view, with phallus removed. B. Ditto, ventral view. C. Ditto, lateral view. D. Phallus, dorsal view. E. Ditto, ventral view. F. Ditto, lateral view.
Fig. 3 in Descriptions of two new Vietomartyria species (Lepidoptera, Micropterigidae) from China
Fig. 3. Male genitalia of Vietomartyria wuyunjiena sp. nov. A. Dorsal view, with phallus removed. B. Ditto, ventral view. C. Ditto, lateral view. D. Phallus, dorsal view. E. Ditto, ventral view. F. Ditto, lateral view.
Figs 6–8 in Two new species of Heleomyzidae (Diptera) from Czech Republic and Crimea
Figs 6–8. Heleomyza kovali sp. nov., male genitalia. 6 – paratype (Crimea), last two abdominal segments and genitalia sublaterally; 7 – holotype (Czech Republic, Jizerské hory PLA), genitalia laterally; 8 – paratype (Crimea), aedeagal complex and hypandrium, dorsal view. For abbreviations see page 268.
Figs 9–14 in Two new species of Heleomyzidae (Diptera) from Czech Republic and Crimea
Figs 9–14. Comparison of males of Eccoptomera nevrlyi sp. nov. and E. ornata Loew, 1862. 9–11, 13–14 – Eccoptomera nevrlyi: 9 – head and thorax, dorsal view; 10 – left wing, lateral view; 11 – hind leg, inner lateral view; 13 – head, anterior view; 14 – head and antennae, lateral view. 12 – E. ornata, basal part of hind leg of E. ornata, inner lateral view.
Figures 10–17. Cyrtinus fisheri. 10–13 in Taxonomic notes on Western Hemisphere Cyrtinini (Coleoptera: Cerambycidae: Lamiinae) including description of two new Cyrtinus LeConte species
Figures 10–17. Cyrtinus fisheri. 10–13) Holotype male. 10) Dorsal habitus. 11) Ventral habitus. 12) Head, frontal view. 13) Lateral habitus. 14–17) Paratype female. 14) Lateral habitus. 15) Head, frontal view. 16) Dorsal habitus. 17) Ventral habitus.
Figures 22–28. Decarthria stephensii. 22–25 in Taxonomic notes on Western Hemisphere Cyrtinini (Coleoptera: Cerambycidae: Lamiinae) including description of two new Cyrtinus LeConte species
Figures 22–28. Decarthria stephensii. 22–25) Female. 22) Dorsal habitus. 23) Ventral habitus. 24) Lateral habitus. 25) Head, frontal view. 26–28) Syntypes, dorsal view.
Figures 29–34. Decarthria spp. 29–32 in Taxonomic notes on Western Hemisphere Cyrtinini (Coleoptera: Cerambycidae: Lamiinae) including description of two new Cyrtinus LeConte species
Figures 29–34. Decarthria spp. 29–32) Decarthria stephensii, labels of the syntypes. 33) Decarthria albofasciata, lectotype, dorsal habitus. 34) Decarthria boricua, holotype male, dorsal habitus.
Figures 25–30 in Provisional revision of the genus Odontocera Audinet-Serville, 1834 (Coleoptera: Cerambycidae). I: exclusions, new rank, synonymies and the description of two new genera
Figures 25–30. Species of Odontocroton (Group B (ii)). 25) Odontocroton quinquecallosus (Zajciw, 1963), holotype, male. 26) Odontocroton septemtuberculatus (Zajciw, 1963), holotype male. 27–30. Odontocroton quinquecallosus. 27) Male, dorsal aspect. 28) Male, ventral aspect. 29) Female, dorsal aspect. 30) Female, ventral aspect.
Fig. 7 in Reproduction of two loricariid species in a confined river and implications for environmental impacts of dams
Fig. 7. Monthly changes in mean (± SE) gonadosomatic index (GSI; dots represent individual values) of Hemiancistrus fuliginosus (a. females; c. males) and Hypostomus isbrueckeri (b. females; d. males). Results of the Kruskal-Wallis tests: Hem. fuliginosus females, H = 47.5, df = 7, p <0.001; males, H = 6.9, df = 7, p <0.44; Hyp. isbrueckeri females, H = 14.4, df = 7, p <0.045, males H = 20.4, df = 7, p <0.005.
Figures 1–2. Zelenka holotypes. 1 in Generic changes in the stag beetle tribe Aesalini (Coleoptera: Lucanidae: Aesalinae) with the description of two new species
Figures 1–2. Zelenka holotypes. 1) Holotype of Echinoaesalus jaechi Zelenka. a) Dorsal habitus. b) Abdomen, ventral view. c) Labels. 2) Holotype female of Echinoaesalus sabahensis Zelenka. a) Dorsal habitus. b) Abdomen, ventral view, showing complete leg-shaped sulci. c) Labels. Photos courtesy H. Schillhammer (Naturhistorisches Museum, Vienna).
Figures 8–9. Trogellus Paulsen species. 8 in Generic changes in the stag beetle tribe Aesalini (Coleoptera: Lucanidae: Aesalinae) with the description of two new species
Figures 8–9. Trogellus Paulsen species. 8) Trogellus trajectus Paulsen, new species, holotype male. a) Dorsal habitus. b) Oblique lateral habitus. c) Labels of holotype. d) Male genitalia. ventral view. 9) Trogellus maesi Paulsen, male. a) Dorsal habitus. b) Male genitalia, ventral view.
Fig. 2 in Discrimination of habitat use between two sympatric species of mullets, Mugil curema and Mugil liza (Mugiliformes: Mugilidae) in the rio Tramandaí Estuary, determined by otolith chemistry
Fig. 2. Means and standard deviations (SD) of (a) Sr86:Ca43 (mmol.mol-1); and (b) Ba137:Ca43 ratio (µmol.mol-1) in otoliths of the inner 20 measurements (core) and the outer 20 measurements (edge) of Mugil curema and M. liza caught in the Tramandaí River Estuary, Brazil. Different letters within a spruce stand denote significant differences between species (Mann-Whitney U test, p<0.05).
Fig. 4 in Discrimination of habitat use between two sympatric species of mullets, Mugil curema and Mugil liza (Mugiliformes: Mugilidae) in the rio Tramandaí Estuary, determined by otolith chemistry
Fig. 4. Otolith transects of Mugil liza measured by LA-ICP-MS from the core to the edge. Ba137:Ca43 (line) and Sr86:Ca43 (dashed line). The identification code and total length (mm) of each fish are indicated on the graph.
Fig. 3 in Discrimination of habitat use between two sympatric species of mullets, Mugil curema and Mugil liza (Mugiliformes: Mugilidae) in the rio Tramandaí Estuary, determined by otolith chemistry
Fig. 3. Otolithtransectsof Mugilcurema measuredbyLA-ICP-MSfromthecoretotheedge. 43 (line) 86 43 (dashedline). Theidentificationcodeand totallength (mm) ofeachfishareindicatedonthegraph.
Fig. 19 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland
Fig. 19. Tenuibiotus zandrae sp. nov. Egg chorion morphology seen in SEM. A. Entire egg. B. Magnification of the egg surface. C–F. Details of the egg processes and surface between them. Filled flat arrowheads indicate thickenings/striae on the surface between processes and filled indented arrowheads indicate small tubercles on the process walls. Scale bars in μm.
Fig. 18 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland
Fig. 18. Tenuibiotus zandrae sp. nov. Egg chorion morphology seen in PCM. A. Midsection under 400× magnification. B. Surface under 400× magnification. C–D. Surface between processes under 1000× magnification. E–H. Midsections of processes of four different eggs under 1000× magnification. Filled flat arrowheads indicate thickenings/striae which are visible as dark dots and lines on the surface between processes. Scale bars in μm.
Fig. 14 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland
Fig. 14. Tenuibiotus zandrae sp. nov. Claws (paratypes). A–B. Claws II and IV seen in PCM, respectively. C–D. Claws I and IV seen in SEM, respectively. Filled indented arrowhead indicates horseshoe structure connecting the anterior and the posterior claw. Scale bars in μm.
Fig. 11 in Integrative taxonomy identifies two new tardigrade species (Eutardigrada: Macrobiotidae) from Greenland
Fig. 11. Tenuibiotus zandrae sp. nov. Body granulation seen in PCM (paratypes). A–B. Uniformly distributed granulation on the dorso-cephalic and dorso-caudal part of the body. C–D. Uniformly distributed granulation on the dorso-cephalic and dorso-caudal part of the body with small, random patches of lacking granulation. E–F. Uniformly distributed granulation on the ventral side of the body without and with small random patches lacking granulation, respectively. A–B, E and C–D, F are from two different paratypes. Scale bars in μm.
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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.