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80 results for “subterranean biodiversity”
Figure 1 in Cryptops (Trigonocryptops) didi sp. n. (Chilopoda: Scolopendromorpha: Cryptopidae): expanding the cryptopid biodiversity in a Brazilian hotspot of subterranean fauna
Figure 1. (a) Geological and distribution map of Cryptops (T.) didi sp. n. in the Upper Ribeira karst area, south-eastern Brazil; (b) view of the Atlantic Rainforest near Lage Branca Cave. Photo: Bruno D. Lenhare.
Figure 5 in Cryptops (Trigonocryptops) didi sp. n. (Chilopoda: Scolopendromorpha: Cryptopidae): expanding the cryptopid biodiversity in a Brazilian hotspot of subterranean fauna
Figure 5. Cryptops (T.) didi sp. n. Holotype (LES – UFSCAR 0026263). (a) Tergite 21; (b) sternite 21 and ultimate legs; (c) sternite 4.
Figure 7 in Cryptops (Trigonocryptops) didi sp. n. (Chilopoda: Scolopendromorpha: Cryptopidae): expanding the cryptopid biodiversity in a Brazilian hotspot of subterranean fauna
Figure 7. Cryptops (T.) didi sp. n. Holotype (LES – UFSCAR 0026263). (a) Lateral view of leg 12; (b) ultimate legs; (c) ultimate leg showing the length, lateral view; (d) tibia and tarsus 1 showing the saw teeth; (e) tibia showing the 19 saw teeth; (f) tarsus showing the 7 saw teeth.
Figure 4 from: García R, Andújar C, Oromí P, López H (2020) Oromia orahan (Curculionidae, Molytinae), a new subterranean species for the Canarian underground biodiversity. Subterranean Biology 35: 1-14. https://doi.org/10.3897/subtbiol.35.52583
Figure 4 Structures of Oromia orahan sp. nov. (letters without asterisks) and O. aguiari (letters with asterisks) A pronotum B aedeagus Cspiculum ventraleD tegmen.
Figure 2 from: García R, Andújar C, Oromí P, López H (2020) Oromia orahan (Curculionidae, Molytinae), a new subterranean species for the Canarian underground biodiversity. Subterranean Biology 35: 1-14. https://doi.org/10.3897/subtbiol.35.52583
Figure 2 Structures of the male and female genitalia of Oromia orahan sp. nov. A aedeagus in dorsal and lateral view B spiculum gastrale C tegmen D spiculum ventrale E ovipositor. Scale bars: 1 mm (A–C), 0.8 mm (D), 0.03 mm (E).
Figure 3 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics
Figure 3. Activity dynamics of isopod Ligidium germanicum (LIGE); diplopods Mecogonopodium carpathicum (MECA), Polydesmus denticulatus (PODE), Trachysphaera acutula (TRAC); and centipedes Harpolithobius anodus (HAAN), Lithobius forficatus (LIFO), during the period November 2008– November 2009.
Figure 2 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics
Figure 2. The non-metric multidimensional scaling ordination analysis (NMS) diagram of Isopoda and Myriapoda collected during both sampling periods; variance explained by axes 1 and 2 as 87.0% and 8.7%, respectively (triangles – depths, dots – species). Abbreviations: i – Isopoda: LIGE – Ligidium germanicum, MEGR – Mesoniscus graniger, TRCA – Trichoniscus carpaticus; d – Diplopoda: JUCU – Julus curvicornis, LEMA – Leptoiulus mariae, LETR – L. trilobatus, MECA – Mecogonopodium carpathicum, POCO – Polydesmus complanatus, PODE – Polydesmus denticulatus, TRAC – Trachysphaera acutula, STST – Strongylosoma stigmatosum; c – Chilopoda: HAAN – Harpolithobius anodus, LI - Lithobius sp. juv., LIFO – Lithobius forficatus, LILU – Lithobius lucifugus; STAC – Strigamia acuminata, STTR – Strigamia transsilvanica.
Supplementary material 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Table S1
Figure 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 1 Location of the study sites. 1 Doline next to Silická ľadnica Ice Cave 2 Vysoká Hill (both sites in Slovak Karst National Park) 3 Drienok Valley (Revúcka Highlands) 4 Belinské skaly (Cerová vrchovina Highlands) 5 Okopanec Hill (Malé Karpaty Mts.) 6–8 Three localities near the Zbrašov Aragonite Caves and Hůrka u Hranic (Moravian-Silesian Foothills) 9–11 Three localities in Chrudim region (Iron Mts.).
Supplementary material 2 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Table S2
Figure 4 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 4 Graphical presentation of myriapod community characteristics in different fixative solutions (N = number of individuals). A Formaldehyde to ethylene glycol ratio of sampled centipede species from all study sites, where both fixating solutions were used B formaldehyde to ethylene glycol ratio of sampled millipede species from all study sites, where both fixating solutions were used.
Figure 2 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 2 A Overall depth distribution of centipede individuals and species B values of Shannon's diversity index and Pielou's evenness index, calculated for centipedes, at each of the study sites C mean values of Shannon's diversity index (±SD) calculated for centipedes, at each depth of the gradient (summarised data from all localities) D overall depth distribution of millipede individuals and species E values of Shannon's diversity index and Pielou's evenness index, calculated for millipedes, at each of the study sites F mean values of Shannon's diversity index (±SD) calculated for millipedes, at each depth of the gradient.
Figure 5 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 5 Vertical distribution of myriapods along the depth gradient in different fixative solutions (data recalculated for the same number of traps). Trend line: dashed = formaldehyde, dotted = ethylene glycol. A Vertical distribution of Chilopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions B vertical distribution of centipede species along the depth gradient at five scree slopes in different fixative solutions C vertical distribution of Diplopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions D vertical distribution of millipede species along the depth gradient at five scree slopes in different fixative solutions.
Figure 3 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 3 Generalised Additive Models of depth distribution pattern of A centipedes and B millipedes. Only species with significant pattern are illustrated. (F-values, * p < 0.05, ** p < 0.01): ALamyctes emarginatus (13.1**), Lithobius forficatus (17.2**), Lithobius lucifugus (5.0*), Lithobius nodulipes (9.7**) BArchiboreoiulus pallidus (22.7**), Cylindroiulus nitidus (5.4*), Glomeris connexa (5.4*), Hylebainosoma tatranum (5.4*), Leptoiulus proximus (7.3*), Mastigona bosniensis (10.5**), Megaphyllum projectum (5.4*), Melogona transsylvanica (15.2**), Polydesmus complanatus (13.1**), Trachysphaera acutula (5.4*), Unciger foetidus (4.9*).
Figure 7 from: Tang D, Eberhard SM (2016) Two new species of Nitocrella (Crustacea, Copepoda, Harpacticoida) from groundwaters of northwestern Australia expand the geographic range of the genus in a global hotspot of subterranean biodiversity. Subterranean Biology 20: 51-76. https://doi.org/10.3897/subtbiol.20.10389
Figure 7 - Nitocrella karanovici sp. n., adult female: A right leg 1 with endopod disarticulated from basis, anterior B left leg 2, anterior C left leg 3, anterior D left leg 4 (note: outer seta on basis is broken off), anterior E right leg 5, ventral. Scale bars: A, B, C, D 50 µm; E 10 µm.
Figure 2 from: Tang D, Eberhard SM (2016) Two new species of Nitocrella (Crustacea, Copepoda, Harpacticoida) from groundwaters of northwestern Australia expand the geographic range of the genus in a global hotspot of subterranean biodiversity. Subterranean Biology 20: 51-76. https://doi.org/10.3897/subtbiol.20.10389
Figure 2 - Nitocrella knotti sp. n., adult female: A habitus, dorsal B urosomites 2–5 and caudal rami, ventral C anal somite and caudal rami, dorsal D rostrum, dorsal E right antennule with segments 3, 5 and 6 shown separately and aesthetasc indicated by arrowhead, ventral F left antenna with one apical element shown separately, anterior. Scale bars: A 200 µm; B 100 µm; C, E, F 25 µm; D 2 µm.
Figure 3 from: Tang D, Eberhard SM (2016) Two new species of Nitocrella (Crustacea, Copepoda, Harpacticoida) from groundwaters of northwestern Australia expand the geographic range of the genus in a global hotspot of subterranean biodiversity. Subterranean Biology 20: 51-76. https://doi.org/10.3897/subtbiol.20.10389
Figure 3 - Nitocrella knotti sp. n., adult female: A labrum, posterior B left mandible, anterior C left maxillule, anterior D left maxilla, anterior E right maxilliped, posterior F left leg 1, anterior G left leg 2, anterior. Scale bars: A, B, C, D, E 20 µm; F, G 50 µm.
Figure 4 from: Tang D, Eberhard SM (2016) Two new species of Nitocrella (Crustacea, Copepoda, Harpacticoida) from groundwaters of northwestern Australia expand the geographic range of the genus in a global hotspot of subterranean biodiversity. Subterranean Biology 20: 51-76. https://doi.org/10.3897/subtbiol.20.10389
Figure 4 - Nitocrella knotti sp. n., adult female: A right leg 3, anterior B right leg 4, anterior C left leg 5, ventral D terminal exopodal segment of left leg 1, anterior E terminal exopodal segment of right leg 2, anterior. Scale bars: A, B 50 µm; C, D 20 µm; E 25 µm.
Figure 1 from: Tang D, Eberhard SM (2016) Two new species of Nitocrella (Crustacea, Copepoda, Harpacticoida) from groundwaters of northwestern Australia expand the geographic range of the genus in a global hotspot of subterranean biodiversity. Subterranean Biology 20: 51-76. https://doi.org/10.3897/subtbiol.20.10389
Figure 1 - A Map showing the species of Nitocrella reported from Western Australia B Enlarged map of the Ethel Gorge area showing sampled boreholes and collection sites for Nitocrella karanovici sp. n. in relation to surface drainage and mine pits.
Figure 6 from: Tang D, Eberhard SM (2016) Two new species of Nitocrella (Crustacea, Copepoda, Harpacticoida) from groundwaters of northwestern Australia expand the geographic range of the genus in a global hotspot of subterranean biodiversity. Subterranean Biology 20: 51-76. https://doi.org/10.3897/subtbiol.20.10389
Figure 6 - Nitocrella karanovici sp. n., adult female: A right antennule with segments 3, 5, 6 and 7 shown separately and aesthetasc indicated by arrowhead, ventral B right antenna, anterior C labrum, posterior D left mandible, posterior E left maxillule, anterior F left maxilla, anterior G right maxilliped, posterior. Scale bars: A 50 µm; B, C 20 µm; D, E, F, G 10 µm.
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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)
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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.