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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 in Aquatic macroinvertebrate assemblages associated with root masses of water hyacinths, Eichhornia crassipes (Mart.) Solms-Laubach, 1883 (Commelinales: Pontederiaceae) in Taabo Lake, Ivory Coast
Figure 2. (Continued).
Figure 4 in Aquatic macroinvertebrate assemblages associated with root masses of water hyacinths, Eichhornia crassipes (Mart.) Solms-Laubach, 1883 (Commelinales: Pontederiaceae) in Taabo Lake, Ivory Coast
Figure 4. (Continued).
Figure 3 in Nematode assemblages from submarine caves in Hong Kong
Figure 3. Mean relative abundance (n53) of nematode feeding groups at the study sites.
Figure 1 in Demersal faunal assemblages in the deep waters of the eastern Ionian Sea
Figure 1. Map of the study area in the eastern Ionian Sea showing the sampling stations.
Fig. 1 in Influence Of Environmental Cycles Upon A Seagrass Caridean Shrimp Assemblage
Fig. 1. Location of the study sites on Hoga Island in the Wakatobi National Park (WNP), south-east Sulawesi, Indonesia.
Fig. 2 in Do habitat, month and environmental parameters affect shrimp assemblage in a shallow semi-enclosed tropical bay, Thailand?
Fig. 2. Relative density (%) and species richness of shrimps collected at different habitats in Pattani Bay between February 2011–January 2012
Fig. 6 in Diversity And Assemblage Patterns Of Juvenile And Small Sized Fishes In The Nearshore Habitats Of The Gulf Of Thailand
Fig. 6. Changes in (a) water temperature, (b) pH, (c) DO, (d) salinity and (e) transparency in each habitat during the study period.
Fig. 11 in Taxonomic Composition And Systematics Of Late Cretaceous Lizard Assemblages From Ukhaa Tolgod And Adjacent Localities, Mongolian Gobi Desert
Fig. 11. Phrynosomimus asper: A, B, IGM 3/81, nearly complete skull with mandibles (articulated with several vertebrae and partial pectoral girdle), dorsal and ventral views.
Fig. 3 in Taxonomic Composition And Systematics Of Late Cretaceous Lizard Assemblages From Ukhaa Tolgod And Adjacent Localities, Mongolian Gobi Desert
Fig. 3. Ctenomastax parva, new genus and species: A, B, IGM 3/61 (holotype), incomplete skull with mandibles from Zos, ventral and dorsal views.
Supplementary material 1 from: Pissaridou P, Cantonati M, Bouchez A, Tziortzis I, Dörflinger G, Vasquez MI (2021) How can integrated morphotaxonomy- and metabarcoding-based diatom assemblage analyses best contribute to the ecological assessment of streams? Metabarcoding and Metagenomics 5: e68438. https://doi.org/10.3897/mbmg.5.68438
Table S1
Supplementary material 2 from: Pissaridou P, Cantonati M, Bouchez A, Tziortzis I, Dörflinger G, Vasquez MI (2021) How can integrated morphotaxonomy- and metabarcoding-based diatom assemblage analyses best contribute to the ecological assessment of streams? Metabarcoding and Metagenomics 5: e68438. https://doi.org/10.3897/mbmg.5.68438
Figure S1
ScienceDex guides
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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.