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183 results for “cave fauna”
Figure 4 from: Deharveng L, Jantarit S, Satasook C (2014) Cyphoderus (Cyphoderidae) as a major component of collembolan cave fauna in Thailand, with description of two new species. ZooKeys 368: 1-21. https://doi.org/10.3897/zookeys.368.6393
Figure 4 - Cyphoderus songkhlaensis sp. n. continued A chaetae of tergites drawn from optical microscope, except 5* derived from SEM image B chaetotaxy of tergites with types of S-chaetae S1 to S4 C trichobothrial complexes of Abd.II D trichobothrial complexes of Abd.III E anterior trichobothrial complexes of Abd.IV F tandem of chaetae on Abd.IV; the smallest is a short type-5 mes and the largest a S4 sens.
Figure 1 from: Deharveng L, Jantarit S, Satasook C (2014) Cyphoderus (Cyphoderidae) as a major component of collembolan cave fauna in Thailand, with description of two new species. ZooKeys 368: 1-21. https://doi.org/10.3897/zookeys.368.6393
Figure 1 - Sampling locations of cave Cyphoderidae in Thailand. Blue empty circles = caves without cyphoderids; red half–circles = caves with cyphoderids; C1, Cyphoderus songkhlaensis sp. n.; C2, unidentified species (Tham Nam Pray, Huay Yod District, Trang Province); C3, unidentified species (Tham Phung, Kiri Rat Nikhom District, Surat Thani Province); C4, unidentified species (Tham Phra, Patil District, Chumphon Province); C5, Cyphoderus khaochakanus sp. n., C6, unidentified species (Tham Kaeo, Pakdee Chumphon District, Chaiyaphum Province); C7, unidentified species (Tham Phupha Yatha Wararam, Muang Loei District, Loei Province); C8, unidentified species (Tham Mae U-Su, Tha Song Yang District, Tak Province).
Figure 6 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 6 - Spatial variations in relative abundance of main invertebrates groups along the gradient of subterranean environmental conditions. (X-axis: 0 — the cave entrance area, negative values — epigean zone, positive values — cave zone). A Cave Abrskila B Cave Golova Otapa.
Figure 1 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 1 - Map of the study regions of Abkhazia. Caves: 1 New Athos 2 Simona Kananita 3 Nizhnyaya Shakuranskaya 4 Srednyaya Shakuranskaya 5 Tsebel'dinskaya 6 Abrskila 7 Golova Otapa 8 Well Uapatyh 9 Well 85 m.
Figure 3 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 3 - Map of Cave Golova Otapa. Sampling stations marked by red points (accordingly Grigorjan 1973).
Figure 2 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 2 - Map of Cave Abrskila. Sampling stations marked by red points (accordingly Benze et al. 1965).
Figure 5 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 5 - Spatial variations in abundance and species richness of the fauna along the gradient of subterranean environmental conditions. (X-axis: 0 — the cave entrance area, negative values — epigean zone, positive values — cave zone). A Cave Abrskila B Cave Golova Otapa.
Figure 4 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 4 - Map of Cave New Athos. Sampling stations marked by red points (accordingly Abhastur 2009).
Figure 7 from: Chertoprud ES, Palatov DM, Borisov RR, Marinskiy VV, Bizin MS, Dbar RS (2016) Distribution and a comparative analysis of the aquatic invertebrate fauna in caves of the western Caucasus. Subterranean Biology 18: 49-70. https://doi.org/10.3897/subtbiol.18.8648
Figure 7 - Two-dimensional ordination with superimposed clusters of the stygobiotic faunas from different caves, based on Kulszinski similarity index. River valleys are shown by different colors. Caves: 1 New Athos 2 Simona Kananita 3 Nizhnyaya Shakuranskaya 4 Srednyaya Shakuranskaya 5 Tsebel'dinskaya 6 Abrskila 7 Golova Otapa 8 Well Uapatyh 9 Well 85 m.
Figure 6 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 6 Boholina laorsriae sp. nov. female: AP1BP2CP3DP4EP5. Scale bars: 50 μm.
Figure 5 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 5 Boholina laorsriae sp. nov. female: A maxillule B maxilla C maxilliped. Scale bars: 50 μm.
Figure 8 from: Boonyanusith C, Wongkamhaeng K, Athibai S (2020) A new species of Boholina (Crustacea, Copepoda, Calanoida) and a first record for stygobiotic calanoid fauna from a cave in Thailand. ZooKeys 904: 1-22. https://doi.org/10.3897/zookeys.904.37609
Figure 8 Boholina laorsriae sp. nov. male: AP5 caudal view B left rami of P5. Scale bars: 50 μm.
FIGURE 115 in The Cave Fauna of California
FIGURE 115. Samwel Cave map.
FIGURE 23 in Oribatid Fauna (Acari, Oribatida) From The Kumaya Cave Of Iheya Village In Central Ryukyu Arc, South Japan, With A Description Of Several New Species
FIGURE 23: Haplozetes makii sp. nov. A, Dorsal view; B, Ventral view; C, Bothridial region; D, Setae; E, Trochanter IV; F, Pedipalp; G, Tarsus and tibia of leg I.
FIGURE 12 in Anchialine cave-dwelling sponge fauna (Porifera) from La Quebrada, Mexico with the description of the first Mexican stygobiont sponges
FIGURE 12. Diplastrella cozumella sp. nov. a) Holotype CNPGG‒1496 in vivo; b) surface with protruding tylostyles (ethanol); c) overall set of spicules (LM); d) tylostyle endings (LM); e) diplaster to spheraster (SEM); f) tylostyle with blunt end (LM); g) tylostyles with multilobed tylo, and concave endings (SEM).
FIGURE 10 in Anchialine cave-dwelling sponge fauna (Porifera) from La Quebrada, Mexico with the description of the first Mexican stygobiont sponges
FIGURE 10. Neosiphonia microtriaeneae sp. nov. a) Holotype CNPGG-1487 (ethanol); b) skeletal arrangement (transversal section, LM); c) ectosomal skeleton (tangential section, SEM).
FIGURE 6 in Anchialine cave-dwelling sponge fauna (Porifera) from La Quebrada, Mexico with the description of the first Mexican stygobiont sponges
FIGURE 6. Svenzea germanyanezi sp. nov. a) Holotype CNPGG‒2342 (ethanol); b) choanosomal skeleton (cross section, LM); c) granulous cells (LM); d) ectosomal skeleton, note the dermis and punctate surface at the upper flank (tangential section, LM); e) strongyles (LM); f) common spicule oxea II (LM); g) thinner oxea I (LM).
FIGURE 8 in Anchialine cave-dwelling sponge fauna (Porifera) from La Quebrada, Mexico with the description of the first Mexican stygobiont sponges
FIGURE 8. Cinachyrellla kuekenthali (Uliczca, 1929). a) CNPGG‒1479 (ethanol); b) eggs setting around porocalice; c-d) choanosomal skeleton (cross section, LM).
FIGURE 5 in Anchialine cave-dwelling sponge fauna (Porifera) from La Quebrada, Mexico with the description of the first Mexican stygobiont sponges
FIGURE 5. Haliclona (Halichoclona) chankanaabiis sp. nov. a) sponge in situ; b) Holotype CNPGG‒1631 (ethanol), note the osculum on top; c) ectosomal skeleton (tangential section, LM); d) choanosomal skeleton (cross section, LM); e) strongyle spicules (LM); f) oxea spicule (LM).
FIGURE 7 in Anchialine cave-dwelling sponge fauna (Porifera) from La Quebrada, Mexico with the description of the first Mexican stygobiont sponges
FIGURE 7. Siphonidium ramosum (Schmidt, 1870). a) CNPGG‒1624 habitus, CNPGG‒1625 (ethanol), notice the two siphonlike apertures; b) skeletal detail assembled by desmas (SEM); c) tetraclone desmas with smooth clones (SEM); d) tetraclone desmas with warty clones (LM); e) spined tylos of tylostyles (SEM).
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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.