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FIGURE 10 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 10. Clypeocaenis multisetosa Soldán, 1978, from Xe Nou River, Xe Bang Hieng River, and outlet Stream of Nam Xouang Resurvoir, Lao PDR, A. Forefemur. B. Mid femur. C. Hind femur. D. Foreclaw. E. Mid claw. F. Hind claw. Scale bars: A, B = 500 μm; C = 400 μm; D–F = 100 μm.
FIGURE 13 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 13. Habitats of the genus Clypeocaenis Soldán, 1978 in Lao PDR, A. Xe Nou River, Xebangfai District, Khammouane Province. B. Tha Hao Stream, Xaybury District, Savannakhet Province. C. Xe Bang Hieng River, Songkhone District, Savannakhet Province. D. Outlet Stream of Nam Xouang Reservoir, Naxaythong District, Vientiane Capital.
FIGURE 6 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 6. Clypeocaenis oligosetosa Soldán, 1983 observed in the Xe Nou River, Lao PDR, A. Dorsal view of the head capsule. B. Labrum. C. Mandibles. D. Maxillae. E. Hypopharynx. F. Labium. Scale bars: A = 1 mm; B, E = 200 μm; C, D = 300 μm; F = 400 μm.
FIGURE 5 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 5. Clpeocaenis laosensis sp. nov., A. Gills III, IV. B. Egg, arrow indicate the micropyle. C. Epithema. D. Detail of the micropyle. Scale bars: A = 500 μm; B = 100 μm; C = 40 μm; D = 30 μm.
FIGURE 9 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 9. Clypeocaenis multisetosa Soldán, 1978, collected from Xe Nou River, Xe Bang Hieng River, and outlet Stream of Nam Xouang Resurvoir in Lao PDR, A. Head capsule. B. Labrum. C. Mandibles. D. Maxillae. E. Hypopharynx. F. Labium. Scale bars: A, D (left maxillary palp) = 500 μm; B, C (right mandible), E = 200 μm; C (left mandible) = 300 μm; D, F (right maxillary palp) = 400 μm.
FIGURE 12 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 12. Microtrichia bands on the ventral side of the operculate gill, as previously documented. A. Clypeocaenis soldani. B. Clypeocaenis multisetosa. C. Clypeocaenis oligosetosa. D. Clypeocaenis kaveri. E. Clypeocaenis afrosetosa. F. Clypeocaenis laosensis sp. nov. G. Mekongellina sangpradubae.
FIGURE 14 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 14. Geographic distribution of the Clypeocaenis laosensis sp. nov. (circle), C. oligosetosa (star); C. multisetosa (triangle).
FIGURE 1 in Contribution to the genus Clypeocaenis Soldán, 1978 (Ephemeroptera: Caenidae) from Lao People's Democratic Republic with a key to Oriental species
FIGURE 1. Clypeocaenis laosensis sp. nov., habitus. A. Female larva. B. Male larva. Scale bars: 1 mm.
FIGURE 7. Holotype female Atopotrophos spiniger. A. Face. B. Head laterally. C. Head dorsally. D. Mesosoma laterally. E. Propodeum. F. Mandibles ventrally. G. T1 dorsally. H. T1 laterally. I in Review of Oriental species of the genus Atopotrophos (Hymenoptera: Ichneumonidae)
FIGURE 7. Holotype female Atopotrophos spiniger. A. Face. B. Head laterally. C. Head dorsally. D. Mesosoma laterally. E. Propodeum. F. Mandibles ventrally. G. T1 dorsally. H. T1 laterally. I. Wings.
FIGURE 5. Holotype female Atopotrophos chinensis. A. Face. B. Head dorsally. C. Propodeum. D. T1 in Review of Oriental species of the genus Atopotrophos (Hymenoptera: Ichneumonidae)
FIGURE 5. Holotype female Atopotrophos chinensis. A. Face. B. Head dorsally. C. Propodeum. D. T1 dorsally.
FIGURE 1. A in Review of Oriental species of the genus Atopotrophos (Hymenoptera: Ichneumonidae)
FIGURE 1. A. Distribution of Atopotrophos bubeng sp. nov. A. chinensis, and A. spiniger. B. Malaise trap and sampling site at Bubeng (Mueang La, Xishuangbanna, Yunnan Province, China, photo by Huang Xiao). C. A. bubeng sp. nov. collection locality at Bubeng (Mueang La, Xishuangbanna, Yunnan Province, China, photo by Huang Xiao).
FIGURES 9–15 in New species and records of Paraphloeostiba Steel, 1960 and Xanthonomus Bernhauer, 1926 from the eastern Palaearctic, Oriental and Papuan regions (Coleoptera: Staphylinidae: Omaliinae)
FIGURES 9–15. Paraphloeostiba zingiberiphila: 9—aedeagus, parameral view, 10—aedeagus, lateral view, 11—male abdominal tergite VIII, 12—male abdominal sternite VIII, 13—female abdominal tergite VIII, 14—female abdominal sternite VIII, 15—spermatheca. Scale bars: 0.1 mm.
FIGURES 1–4 in New species and records of Paraphloeostiba Steel, 1960 and Xanthonomus Bernhauer, 1926 from the eastern Palaearctic, Oriental and Papuan regions (Coleoptera: Staphylinidae: Omaliinae)
FIGURES 1–4. Paraphloeostiba acrolochaoides: 1—aedeagus, parameral view, 2—aedeagus, lateral view, 3—male abdominal tergite VIII, 4—male abdominal sternite VIII. Scale bars: 0.1 mm.
FIGURES 5–8 in New species and records of Paraphloeostiba Steel, 1960 and Xanthonomus Bernhauer, 1926 from the eastern Palaearctic, Oriental and Papuan regions (Coleoptera: Staphylinidae: Omaliinae)
FIGURES 5–8. Paraphloeostiba breviuscula: 5—aedeagus, parameral view, 6—aedeagus, lateral view, 7—male abdominal tergite VIII, 8—male abdominal sternite VIII. Scale bars: 0.1 mm.
Ciência Vitae controlled vocabulary - Type of Orientation
Open the record for dataset details and reuse information.
Data from: Seasonal contrasts in individual consistency of oriental honey buzzards' migration
Individual consistency in migration can shine light on the mechanisms of migration. Most studies reported that birds are more consistent in the timing than in the routes or stopover sites during migration, but some specialist species showed the opposite patterns, being more consistent in spatial than temporal aspects of migration. One possible explanation for this contrast is that specialists rely on particular food or habitat resources, which restrict the migratory routes they can take, leading to high spatial consistency. If this is the case, the effect of specialist foraging should become apparent only when birds forage, instead of fasting and flying continuously. To test this effect, we analysed individual consistency in migration of the oriental honey buzzard (Pernis ptilorhynchus), a specialist raptor that feeds on honeybees and wasps, using a long-term tracking data set. As honey buzzards make extended stopovers during which they forage in spring but not in autumn, the spatial consistency should be higher in spring than in autumn. Honey buzzards were highly consistent in both their migratory routes and stopover sites in Southeast Asia, but only during spring migration. Our results highlight an important link between species' migratory consistency and foraging ecology.
FIGURES 1–5 in Morphology of the last instar larva and pupa of Synanthedon caucasica (Gorbunov 1986) (Lepidoptera: Sesiidae), a serious pest of oriental plane and elm trees
FIGURES 1–5. Larva of Synanthedon caucasica. Head capsule – 1. Frontal view, 2. Lateral view, 3. Mandible – the last instar larva, 4. Mandible – the third instar larva, 5. Setal map of thorax (T1–3) and abdomen (A1–A9) segments. Scale bar: 1, 2 – 0.5 mm; 3, 4 – 0.25 mm.
FIGURES 6–11 in Morphology of the last instar larva and pupa of Synanthedon caucasica (Gorbunov 1986) (Lepidoptera: Sesiidae), a serious pest of oriental plane and elm trees
FIGURES 6–11. Scanning electron micrographs of larva of Synanthedon caucasica: 6. Third segment of maxillary palpus, 7. Antenna, 8. Crochets on an larval proleg, 9. Close-up of antenna, 10. Crochets on fourth abdominal proleg, 11. Prothoracic leg. Scale bar: 6 – 1 μm; 7, 8, 9 – 10 μm; 10,11 – 100 μm.
FIGURES 12–18 in Morphology of the last instar larva and pupa of Synanthedon caucasica (Gorbunov 1986) (Lepidoptera: Sesiidae), a serious pest of oriental plane and elm trees
FIGURES 12–18. Morphology of pupa of Synanthedon caucasica: 12. Ventral view, 13. Frons laterally, 14. Frons dorsally, 15. Proboscis and leg ends, 16. Labrum and vicinity, 17. Spines on abdominal segments dorsally, 18. Abdominal end ventrally. Scale bar: 13, 14, 16, 17, 18 – 0,5 mm, 15 – 1 mm 12 – 2 mm.
FIGURES 46–51. Notophlebia jobi. 46–49 in New Oriental tribe Iscini, new non-dilatognathan species of Notophlebia Peters & Edmunds 1970 and independent origin of Dilatognathus-type mouth apparatus in Atalophlebiinae (Ephemeroptera: Leptophlebiidae)
FIGURES 46–51. Notophlebia jobi. 46–49, third segment of maxillary palp (46 and 48, ventral side; 47 and 49, dorsal side); 50–51, base of third segment of labial palp, dorsal side).
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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.