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35 results for “cave streams”
Figure 3 from: Lunghi E, Bruni G, Ficetola F, Manenti R (2018) Is the Italian stream frog (Rana italica Dubois, 1987) an opportunistic exploiter of caves twilight zone? Subterranean Biology 25: 49-60. https://doi.org/10.3897/subtbiol.25.23803
Figure 3 Boxplots indicating differences in the use of cave spaces. Difference between A age classes (Adults/ Juveniles) and B adult sexes (Females/Males) in the use of the subterranean surface area; differences between C age classes and D adult sexes in the use of cave walls. Diagonal bar inside the box represents the median.
Figure 1 from: Lunghi E, Bruni G, Ficetola F, Manenti R (2018) Is the Italian stream frog (Rana italica Dubois, 1987) an opportunistic exploiter of caves twilight zone? Subterranean Biology 25: 49-60. https://doi.org/10.3897/subtbiol.25.23803
Figure 1 Two juveniles of Rana italica: a) during the measurement of SVL and b) climbing cave walls.
Figure 7 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 7 dbRDA ordination for the model of the investigated cave sites (based on Bray–Curtis similarity) factored with distance ranges: 1 – 0–60 m, 2 – 280–380 m, 3 – 460–650 m.
Figure 6 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 6 Changes in the biomass of stygobionts according to the distance from the cave entrance (2018–2019).
Figure 8 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 8 dbRDA ordination for the investigated cave sites during the research in autumn 2019 (based on Bray–Curtis similarity) factored with luminosity ranges: 0 – 0 lx, 1 – 0.07–2.7 lx, 2 – 13.17 lx, 3 – 555 lx.
Figure 3 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 3 Changes in the number of stygoxenes, stygophiles and stygobionts according to the distance from the cave entrance (2018–2019).
Figure 4 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 4 The most numerous stygobionts in the Lower Shakuranskaya Cave AXiphocaridinella osterloffi (Juzbaš'jan, 1941) BPontohoratia birsteini (Starobogatov, 1962).
Figure 1 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 1 A Location of the Lower Shakuranskaya Cave on the map of Abkhazia B sampling stations location scheme in the Lower Shakuranskaya Cave in 2018–2019. In numbers – stations, sampled in February 2018, May and October, 2019; in letters – additional stations, sampled in October, 2019 (for each station indicated numbers of stygobionts, stygophiles and stygoxenes). Views on the cave stream C at station 2 (ecotone zone) D at station 4 E at station 5.
Figure 2 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 2 The variation in the values of Shannon diversity index along the distance from the cave entrance (2018–2019).
Figure 5 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 5 Changes in the biomass of stygoxenes, stygophiles and stygobionts according to the distance from the cave entrance (2018–2019).
Figure 10 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 10 The CCA ordination of hydrobionts species from Nizhnyaya Shakuranskaya Cave. Black points – stygobionts, blue points – stygophiles, green points – stygoxenes. Abbreviations: A gut – A. guttatus, B gem – B. gemellus, C hor – C. horatieformis, C schak – C. schakuranica, C shad – C. shadini, C sp – Caucasopsis sp., Ch abch – C. abchazica, Cn sp – Cnetha sp., E sp – Elmis sp., D sub – D. submaculata, D tau – D. taurocaucasica, Dend sp – Dendrocoelum sp., E ljov – E. cf. ljovuschkini, Es sp – Eisenia sp., E palp – E. palpatus, E zimm – E. zimmermanni, G kom – G. cf. komareki, H gor – H. gordioides, H sang – H. sanguisuga, L col – L. colchicus, L inc – L. incanus, L sp – Leuctra sp., M sp – Macropelopia sp., N abl – N. cf. ablaskiri, N iner – N. inermis, N magn – N. magnus, N mart – N. martynovia, O sp – Odeles sp., P birst – P. birsteini, P lat – P. latissima, Par sp – Parametriocnemus sp., P wern – P. werneri, R som – R. somcheticus, Rh sp – Rhynchelmis sp., S cach – S. cachetica, S clav – S. clavatus, Sty sp – Stylodrilus sp., T cauc – T. caucasica, T valv – T. valvatus, X falc – X. falcirostris, X ost – X. osterloffi, Z yak – Z. yakovi.
Figure 9 from: Borisov RR, Chertoprud ES, Palatov DM, Novichkova AA (2021) Variability in macrozoobenthic assemblages along a gradient of environmental conditions in the stream water of karst caves (Lower Shakuranskaya Cave, western Caucasus). Subterranean Biology 39: 107-127. https://doi.org/10.3897/subtbiol.39.65733
Figure 9 The two-dimensional nMDS ordination of the investigated cave sites, based on Bray–Curtis similarities (stress = 0.09) and factored with luminosity: 0 – 0 lx, 1 – 0.07–2.7 lx, 2 – 13.17 lx, 3 – 555 lx. Dots are labeled: first number – season/year of research: 1 – winter 2018, 2 – spring 2018, 3 – autumn 2019; second number – no of sampling station.
Figure 2 from: Lunghi E, Bruni G, Ficetola F, Manenti R (2018) Is the Italian stream frog (Rana italica Dubois, 1987) an opportunistic exploiter of caves twilight zone? Subterranean Biology 25: 49-60. https://doi.org/10.3897/subtbiol.25.23803
Figure 2 Average monthly observation (±ES) of Rana italica within studied caves.
FIGURE 3 in A radiation of hydrobiid snails in the caves and streams at Precipitous Bluff southwest Tasmania, Australia (Mollusca: Caenogastropoda: Rissooidea: Hydrobiidae s.l.) ,
FIGURE 3: Radulae of Pseudotricula species. A, B, Pseudotricula eberhardi, C.165053, Black Curtain Streamway, Cueva Blanca; C–H, Pseudotricula expandolabra, C, D, C.201495, Persephone Streamway, Bauhaus, E, G, H, C.201811, Persephone Pot, Bauhaus, F, C.201822, main streamway, Bauhaus; I, Pseudotricula arthurclarkei, C.203671, paratype, Quetzalcoatl Conduit; J–L, Pseudotricula conica, C.203676, paratype, Cane Toad Abuse Streamway, Damper Cave. A, C, G, K, central, lateral inner and outer marginal teeth; B, E, L, central teeth; D, outer marginal teeth; F, J, lateral and inner marginal teeth; H, lateral tooth; I, central and lateral teeth. Scales: A, B, E, H–J, L 10 m; C, F, G, K, 20 m; D, 5 m.
FIGURE 12 in A radiation of hydrobiid snails in the caves and streams at Precipitous Bluff southwest Tasmania, Australia (Mollusca: Caenogastropoda: Rissooidea: Hydrobiidae s.l.) ,
FIGURE 12. Shells of Pseudotricula species. A, Pseudotricula arthurclarkei, holotype, C.439656, Quetzalcoatl Conduit; B D, Pseudotricula conica, B, holotype, Cane Toad Abuse Streamway, Damper Cave; C, C.203680, main streamway near entrance, Damper Cave; D, C.201813, Persephone Pot, Bauhaus. Scales: A–D, 500 m.
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Allen Brain Atlas
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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.