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1,164 results for “cave-dwelling”
Fig. 6 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 6. Chiraziulus kaiseri (Mauriès, 1983), female vulva. Scanning electron micrographs. A. Vulva in situ behind second pair of legs, posterior view. B. Details of right vulva behind second pair of legs. C. Detail of microtubular structure under the vulva. D. Vulva in ventral view. E. Vulva in anterior view. Abbreviations: o = operculum; b = bursa. Scale bars: A = 100 μm; B–E = 10 μm.
Fig. 3 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 3. Chiraziulus kaiseri (Mauriès, 1983), paratypes. Scanning electron micrographs. A. Head and first body rings in lateral view. B. Last body rings ("tail") in lateral view. C. Tip of antenna. D. Detail of the limbus; notice lines of beadlike structures between cuticular scutes. E. Detail of labrum in frontal view. F. Gnathochilarium in ventral view; the arrow shows the distomesal setae on stipes. Scale bars: A–B, E–F = 100 μm; C = 10 μm; D = 1 μm.
Fig. 2 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 2. Distribution of species of Chiraziulus Mauriès, 1983 in Iran (Mauriès 1987). C. troglopersicus sp. nov.: red dot (1); C. kaiseri: yellow dots (2–6). 1. Neyneh Cave. 2. "Chiraz" "montagne greseuse au nord de la ville". 3. 19 km W of Shiraz. 4. 5 km N of Persepolis. 5. Oasis 95 km N of Bandarabass. 6. Sarab Cave.
Fig. 9 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 9. Chiraziulus troglopersicus sp. nov., ♂, paratype, gonopods. Scanning electron micrographs. A. Anterior gonopods in posterior view. B. Detail of the process on the tip of an anterior gonopod in posterior view. C. Anterior gonopods in anterior view. D. As C, in apical view. E. Tip of the flagellum. F. Posterior gonopods in lateral view. G. Tip of the long spine-like process of the posterior gonopod. H. Posterior gonopods in posterior view. I. As H, in anterior view. J. Detail of the mesal sternal part of the gonopods. Abbreviations: C = coxal process; T = telepodite; f = flagellum; s = setae; dp = distal process. Scale bars: A–D, F, H–I = 10 μm; E, G, J = 1 μm.
Fig. 8 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 8. Number of podous rings and midbody vertical diameter of the studied specimens. Chiraziulus kaiseri (Mauriès, 1983) in blue; Chiraziulus troglopersicus sp. nov. in red. ▲ = adult ♂♂; ● = juveniles and ♀♀.
Fig. 7 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 7. Chiraziulus kaiseri (Mauriès, 1983). Comparison of the paratype (A, C, E, G, I and K) and specimen from Ghar Sarab Cave (B, D, F, H, J and L). A–B. Left anterior gonopods, mesal view. C–D. Anterior gonopod, posterior view. E–F. Anterior gonopod, anterior view. G–H. Anterior gonopod, lateral view. I–J. Anterior gonopod, apical view. K–L. Posterior gonopods.
Fig. 12 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 12. Chiraziulus kaiseri (Mauriès, 1983), paratypes infected with ectoparasitic fungi of the genus Rickia Cavara, order Laboulbeniales. A. Arrows indicate black dots on the body rings corresponding to the insertion of the fungi. B. Scanning electron micrograph of the collum with one fungus (arrow). Scale bars: A = 1 mm; B = 100 μm.
Fig. 5 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 5. Chiraziulus kaiseri (Mauriès, 1983), ♂, paratypes, gonopods. Scanning electron micrographs. A. Anterior gonopods in anterior view. B. Anterior gonopods with one posterior gonopod in lateral view. C. As B, in apical view. D. As B, in posterior view. E–F. Anterior gonopod with detail of the processes on the tip of anterior gonopods. G–I. Posterior gonopod. J. Detail of the mesal sternal part. Abbreviations: C = coxal process; T = telepodite; Ta = anterior lobe of telopodite; Tb = posterior lobe of telepodite. Scale bars: A, D, I = 100 μm; B–C, E–H = 10 μm.
Fig. 11 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 11. Cambala annulata (Say, 1821), anterior gonopod. A. Mesal view. B. Detail of the mesal sternal part. C. Apical part of coxal processes and telepodite. Scale bars: A = 100 μm; B–C = 10 μm.
Fig. 4 in Highly disjunct and highly infected millipedes - a new cave-dwelling species of Chiraziulus (Diplopoda: Spirostreptida: Cambalidae) from Iran and notes on Laboulbeniales ectoparasites
Fig. 4. Chiraziulus kaiseri (Mauriès, 1983), ♂, paratype, anterior gonopod. Scanning electron micrographs. A. Tip of flagellum. B. Flagellum insertion and loop across anterior gonopod coxite. C. Anterior gonopod showing the entire extension of the flagellum. Scale bars: A = 10 μm; B–C = 100 μm.
Fig. 8 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 8. Coecobrya oculata sp. nov. A. Labrum. B. Dorsal cephalic chaetotaxy. C. Lateral process of labial palp. D. Chaetae on the ventral side of head. E. Trochanteral organ, ventral view. F. Hind claw. G. Anterior face of ventral tube and lateral flap. H. Posterior face of ventral tube. I. Mucro. J. Thoracic chaetotaxy. K–M, Abdominal chaetotaxy. K. Abd. I–III. L. Abd. IV. M. Abd. V. Scale bars: A, C–I = 20 μm; B, J–M = 100 μm.
Fig. 7 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 7. Abdominal chaetotaxy of Coecobrya ciliata sp. nov. A. Abd. I–III. B. Abd. IV. C. Abd. V. Scale bars: 50 μm.
Fig. 6 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 6. Coecobrya ciliata sp. nov. A. Ant. III organ. B. Dorsal cephalic chaetotaxy. C. Lateral process of labial palp. D. Chaetae on the ventral side of head. E. Trochanteral organ, ventral view. F. Hind claw. G. Anterior face of ventral tube ad lateral flap. H. Posterior face of ventral tube. I. Mucro. J. Thoracic chaetotaxy. Scale bars: A, C–I = 20 μm; B, J = 100 μm.
Fig. 3 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 3. Coecobrya gejianbangi sp. nov. A. Thoracic chaetotaxy. B–D. Abdominal chaetotaxy. B. Abd. I–III. C. Abd. IV. D. Abd. V. Scale bars: 200 μm.
Fig. 9. Clypeal chaetae. A. Diagram. B in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 9. Clypeal chaetae. A. Diagram. B. Coecobrya gejianbangi sp. nov. C. Coecobrya annulata sp. nov. D. Coecobrya ciliata sp. nov. E. Coecobrya brevis. F. Coecobrya pani. Figures of the latter two species after Xu et al. (2012). Scale bars: 40 μm.
Fig. 4 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 4. Coecobrya annulata sp. nov. A. Ant. III organ. B. Dorsal cephalic chaetotaxy. C. Chaetae on the ventral side of head. D. Trochanteral organ, ventral view. E. Hind claw. F. Anterior face and lateral flap of ventral tube. G. Posterior face of ventral tube. H. Mucro. Scale bars: A, C–E, H = 50 μm; B, F–G = 100 μm.
Fig. 2 in Cave-dwelling Coecobrya from southern China with a survey of clypeal chaetae in Entomobryoidea (Collembola)
Fig. 2. Coecobrya gejianbangi sp. nov. A. Ant. III organ. B. Dorsal cephalic chaetotaxy. C. Lateral process of labial palp. D. Chaetae on the ventral side of head. E. Trochanteral organ, ventral view. F. Fore claw. G. Hind claw. H–J. Ventral tube. H. Anterior face. I. Posterior face. J. Lateral flap. K. Manubrial plaque. Scale bars: A, C, E–G, K = 40 μm; B, D, H–J = 100 μm.
FIGURES 2A–F. A–B in JIE LIU, SHUQIANG LI & PETER JÄGER (2008) New cave-dwelling huntsman spider species of the genus Sinopoda (Araneae: Sparassidae) from southern China. Zootaxa, 1857, 1-20.
FIGURES 2A–F. A–B. Sinopoda fornicata sp. nov., holotype. C–D. Sinopoda yaojingensis sp. nov., holotype. E–F. Sinopoda crassa sp. nov., holotype. (A, C, E, Epigyne, ventral view; B, D, F, Vulva, dorsal view). Scale lines: 0.2 mm.
Fig. 4 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour
Fig. 4. Scytodid egg-sac. (A) Typical egg-sac of Scytodes cavernarum, S. fusca and the Philippines Scytodes sp. 2; and (B) Scytodes magna egg-sac. Note the denser silk surrounding the eggs of S. magna.
Fig. 8 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour
Fig. 8. Reproductive traits of five cave species of scytodids. (A) Mean (± S.E.) total number of spiderlings per female; (B) mean (± S.E.) egg hatching time (d); (C) mean (± S.E.) interval (d) between clutches; (D) mean (± S.E.) interval (d) between hatching and the next egg-sac production; (E) mean (± S.E.) number of clutches; and (F) mean (± S.E.) number of spiderlings per clutch. Different lower cases indicate significant differences.
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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.