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6,030 results for “Caving”
Fig. 6 in A new genus and two new species of cave-dwelling cyclopoids (Crustacea, Copepoda) from the epikarst zone of Thailand and up-to-date keys to genera and subgenera of the Bryocyclops and Microcyclops groups
Fig. 6. Metacyclops thailandicus sp. nov., holotype, ♀. A. Habitus, with egg sac, dorsal view. B. Urosome, dorsal view. C. Urosome, lateral view. D. Urosome, ventral view. E. P5, lateral view. F. P5, ventral view. Scale bars: 100 μm.
Rakhterā (रखतेरा or Rakhetrā, Ashoknagar). Bhiyāṃdāṃt caves with images of Ādinātha and other deities.
<p>Rakhterā (रखतेरा or Rakhetrā, Ashoknagar). Bhiyāṃdāṃt caves with images of Ādinātha and other deities.</p>
Badoh Pathari (बड़ोह पठारी), Vidisha district, Madhya Pradesh. Caves with Mātṛkā relief panel.
<p>Badoh Pathari (बड़ोह पठारी), Vidisha district, Madhya Pradesh. Caves with Mātṛkā relief panel.</p>
Fig. 2 in The genus Jeekelosoma Mauriès, 1985 - Moroccan cave millipedes (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 2. Jeekelosoma abadi (Mauriès, 1985) comb. nov., topotypes. A–C. Female (NHMD 302022). D–G. Male (NHMD 302021). A. Head and body rings 1–5, lateral view. B. Head and collum, frontal view. C. Body rings 8–10 and posterior half of ring 7, seen from the right. D. Rings 10–11, seen from the left. E. Ring 11 and legs, posterior view. F. Rings 10–11, dorsal view. G. Ozopore from ring 18, right side (anterior to the right). Scale bars: A–F = 0.2 mm; G = 0.02 mm.
Fig. 4 in The genus Jeekelosoma Mauriès, 1985 - Moroccan cave millipedes (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 4. Jeekelosoma abadi (Mauriès, 1985) comb. nov., male topotype (NHMD 302021), left gonopod in situ. A. Ventral view. B. Slightly meso-ventral view to show the keel a. C. Subapical view. D. Lateral view. E. Mesal view. Abbreviations: a = posterior-median keel of gonopod aperture; app = terminal appendage of solenophore; map = mesal acropodital process; prf = prefemoral part; slm = solenomere; sph = solenophore; sph‑a = apical lamella of solenophore. Scale bars: A–B, D–E = 0.05 mm; C = 0.01 mm.
Fig. 3 in The genus Jeekelosoma Mauriès, 1985 - Moroccan cave millipedes (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 3. Jeekelosoma abadi (Mauriès, 1985) comb. nov., male topotype (NHMD 302021). A. Penultimate ring (podous), ultimate ring (apodous) and telson, oblique lateral view. B. Telson, posterior view. C. Midbody leg. D. Claw of midbody leg. Scale bars: A–C = 0.1 mm; D = 0.01 mm.
Fig. 9 in The genus Jeekelosoma Mauriès, 1985 - Moroccan cave millipedes (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 9. Jeekelosoma viginti sp. nov. paratype female (NHMD 302024). A. Rings 8–10, lateral view. B. Ring 9, dorsal view. C. Right ozopore of ring 9. D. Claw of midbody leg. E. Midbody leg. F. Cuticular (fungal?) structures from surface of peritrema. Scale bars: A–B, E = 0.1 mm; C = 0.02 mm; D = 0.01 mm; F = 0.005 mm.
Fig. 1 in The genus Jeekelosoma Mauriès, 1985 - Moroccan cave millipedes (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 1. Jeekelosoma abadi (Mauriès, 1985) comb. nov., living specimen from the type locality. Courtesy of Carles Hernando.
Fig. 6 in The genus Jeekelosoma Mauriès, 1985 - Moroccan cave millipedes (Diplopoda, Polydesmida, Paradoxosomatidae)
Fig. 6. Jeekelosoma heptarachne sp. nov., paratype, male (MZB 71-8589). A. Rings 10–11, dorsal view. B. Rings 10–11, lateral view. C. Rings 10–11, posterior view, with three legs of left side. D. gonopod aperture. E. Tarsus and claw of midbody leg. F. Claw of midbody leg. G–H. Right ozopore of ring 10. Scale bars: A–C = 0.1 mm; D–E = 0.02 mm; F–H = 0.01 mm.
Concordance of the Qumran Cave 4 'Unidentified fragments' on PAM 43691 (IAA # 96)
<p>Lists of agreement with the PAM 43691 (IAA # 96) Qumran Cave 4 unidentified fragments with fragments on earlier photographs in the series of Unidentified fragments (cf. DJD 33) </p>
Fig. 6 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 6. Maximum likelihood (ML) trees of studied Fridericia species based on the ITS region (A), CO1 (B) and H3 genes (C). Bootstrap values greater than 50 are shown at the nodes. Sequences from new species described here appear in bold. A. ML tree of the ITS region based on 821 nucleotide positions. B. ML tree of the CO1 gene based on 388 nucleotide positions. C. ML tree of the H3 gene based on 202 nucleotide positions.
Fig. 1. A–D in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 1. A–D. Fridericia baradlana sp. nov. A–B. Spermathecae. C. Oesophageal appendage. D. Coelomocytes. E–F. Fridericia spelaeophila sp. nov. E. Coelomocytes. F. Spermathecae. Scale bars: 50 μm.
Fig. 2 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 2. Micrograph of Fridericia baradlana sp. nov. A. Brain. B–D. Coelomocytes (C. several large lenticytes). E. Detached chaetae in coelom. F. Thick body wall, thin cuticle. G. Pharyngeal glands (marked with arrows). H. Subneural glands in XIII–XIV (marked with arrows). I–K. Sperm funnels (funnel's body marked with black arrows, sperm head marked with white arrows). (B–C, F, I–K in vivo, A, F, H fixed, stained, D, G fixed, not stained. Scale bars: 50 μm, in D 20 μm. B, E from holotype.)
Fig. 5 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 5. Micrograph of Fridericia spelaeophila sp. nov. A. Sperm funnel. B, H. Spermathecal ampullae (sperm in ampulla marked with arrows). C–G. Spermathecae. (In C, diverticula marked with black arrows, ectal glands with white arrow. D–E. Fused proximal parts marked with white arrows, ectal glands with black arrows. F. Ectal duct marked with white arrow, ectal glands with black arrows. G. Ectal glands marked with white arrow, the refractive sperm in ampullar distal part marked with black arrow). All pictures fixed and stained. E from holotype. Scale bars: 50 μm.
Fig. 7 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 7. Concatenated phylogenetic tree of the two new and other Fridericia species based on 1447 nucleotid positions (which comprise the CO1, H3 genes and the ITS region). Posterior probabilities greater than 50 are shown at the nodes. Sequences from new species described here appear in bold.
Fig. 4 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 4. Micrograph of Fridericia spelaeophila sp. nov. A. Brain. B. Head pore (marked with arrow). C. Chaetae in V–VII. D. Clitellar glands, dorsal view. E. Chaetae in VII–VIII. F. Detached chaetae in coelom. G. Coelomocytes. H. Nephridium at 7/8 (pre- and postseptale marked with arrows). I. Fragments of decaying wood in the intestine (marked with arrow). J. Male copulatory organs, lateral view. K–L. Sperm funnels. (A, K in vivo, B–J, L fixed, stained. Scale bars: 50 μm. B, G from holotype, K from DNA 1283.)
Fig. 3 in Two new species of Fridericia (Annelida: Enchytraeidae) from Hungarian caves
Fig. 3. Micrograph of Fridericia baradlana sp. nov. A. Sperm funnels (marked with arrows). B–C. Male copulatory organs (marked with arrows). D. Bursal slit (marked with arrow). E–H, K–L. Spermathecae. I–J. Spermathecal ectal glands (marked with arrows). (A, C, E–F in vivo, B, J, K–L fixed, stained, D, G, H–I fixed, not stained). Scale bars: 50 μm, in H, J–L 20 μm, J–L from holotype.
Udayagiri (उदयगिरि Madhya Pradesh). Cave 8, exterior.
<p>Udayagiri (उदयगिरि Madhya Pradesh). Cave 8, exterior. </p>
Fig. 20 in Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species
Fig. 20. Tangle of Pleioplectron thomsoni (Chopard, 1923) comb. nov. on cave ceiling. Trotters Gorge, Otago.
Fig. 18 in Diversity and distribution of Pleioplectron Hutton cave wētā (Orthoptera: Rhaphidophoridae: Macropathinae), with the synonymy of Weta Chopard and the description of seven new species
Fig. 18. Known distribution of cave wētā in the genus Pleioplectron Hutton, 1896. A. North Island, New Zealand, showing the distribution of P. hudsoni. B–J. South Island, New Zealand, showing the distribution of the remaining nine species.
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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)
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.