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Figs 6, 7 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil
Figs 6, 7. Insects associated with Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828: 6, female of the cleptoparasitic bee Rhathymus bicolor Lepeletier & Serville, 1828 leaving a nest;7, female of Pseudomethoca sp. walking through the nesting area.
Figs 32–36 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 32–36. Parasitoid of Nisoniades macarius (Herrich-SchÄffer, 1870) larva: 32, parasitized first instar larva; 33, parasitized third instar larva. Pupa of the parasitoid: 34, ventral view; 35, dorsal view. Fig. 36, parasitoid in adult form. The red arrows point to the parasitoid larvae.
Figs 3–6 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 3–6. Egg of Nisoniades macarius (Herrich-SchÄffer, 1870): 3, egg in the adaxial portion of the Ipomoea asarifolia (Desr.) Roem. & Schult. leaf; 4, egg in dorsal view; 5, egg in lateral view close to hatching; 6, egg after hatching.
Figs 4, 5 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil
Figs 4, 5. Brood cells and larva of Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828: 4, lateral view (scale bar 1 cm); 5, brood cell with pre-defecating larva eating the pollen mass (scale bar 1 cm).
Fig. 3 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil
Fig. 3. Nests of Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828 showing the position of the brood cells.
Figs 19–27 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 19–27. Immatures and adults of Nisoniades macarius (Herrich-SchÄffer, 1870). Pre-pupa: 19, dorsal view; 20, lateral view. Pupa: 21, dorsal view; 22, lateral view; 23, ventral view; 24, frontal view. Fig. 25, adult female resting on grass leaf close to the host plant. Dorsal (left) and ventral (right) views of the adults raised in the laboratorY: 26, female; 27, male.
Fig. 7 in Breeding biology and conservation of hawk-eagles (Spizaetus spp.) Aves, Accipitridae) in southern Atlantic Forest, Brazil
Fig. 7. Nesting phenology of Ornate Hawk-Eagle (nest C). Chronological sequence from upper left to bottom right: nest with an egg (27 Sep 2008); egg; (27 Sep 2008); nestling – few days old (08 Nov 2008); adult on nest (16 Nov 2008); nestling about 10 days old (19 Nov 2008); nestling about 20 days old (28 Nov 2008); nestling about 40 days old (Dec 2008); Fledging (Apr 2009); Nest without chamber or traces of use (Apr 2009).
Fig. 6 in Breeding biology and conservation of hawk-eagles (Spizaetus spp.) Aves, Accipitridae) in southern Atlantic Forest, Brazil
Fig. 6. Nest of an Ornate Hawk-Eagle located 31 m in an Araucaria tree (DBH = 132 cm). Lateral view (upper right) and view from above (bottom right) with details of the chamber (with green leaves and sticks).
Fig. 4 in Breeding biology and conservation of hawk-eagles (Spizaetus spp.) Aves, Accipitridae) in southern Atlantic Forest, Brazil
Fig. 4. Nest of an Ornate Hawk-Eagle built 20 m in a Myrtaceae tree (DBH = 78.94 cm) (red circle). Lateral view (upper right) and view from above (bottom right) of the nest.
Fig. 2 in Breeding biology and conservation of hawk-eagles (Spizaetus spp.) Aves, Accipitridae) in southern Atlantic Forest, Brazil
Fig. 2. Extent of occurrence of the Ornate Hawk-Eagle in the southern Atlantic Forest, Brazil based on historical (before 2000s; red triangles and red dashed line) and current records (after 2000s; black dots and line). Atlantic Forest remnants are showed in light green.
Fig. 1 in Breeding biology and conservation of hawk-eagles (Spizaetus spp.) Aves, Accipitridae) in southern Atlantic Forest, Brazil
Fig. 1. Extent of occurrence of the Black-and-white Hawk-Eagle in the southern Atlantic Forest, Brazil based on historical (before 2000s; red triangles and red dashed line) and current records (after 2000s; black dots and line). Atlantic Forest remnants are showed in light green.
Fig. 3 in Breeding biology and conservation of hawk-eagles (Spizaetus spp.) Aves, Accipitridae) in southern Atlantic Forest, Brazil
Fig. 3. Extent of occurrence of the Black Hawk-Eagle in the southern Atlantic Forest, Brazil based on historical (before 2000s; red triangles and red dashed line) and current records (after 2000s; black dots and line). Atlantic Forest remnants are showed in light green.
Fig. 4 in Dung beetles in a Caatinga Natural Reserve: a threatened Brazilian dry-forest with high biological value
Fig. 4. Multidimensional scaling (MDS) ordination of the dung beetle communities in: (a) Riparian Forest (RF), Capoeira (CAP) and Arboreal Caatinga (ARB); (b) Management (MZ) and Preservation Zone (PZ) of the Brazilian National Reserve FLONA Contendas do SincorÁ, state of Bahia.
Fig. 3 in Dung beetles in a Caatinga Natural Reserve: a threatened Brazilian dry-forest with high biological value
Fig. 3. Species richness accumulation curves for the Management zone and Natural resources zone stablished in the management plan of the FLONA Contendas do SincorÁ conservation unit, state of Bahia, Brazil.
Fig. 2 in Dung beetles in a Caatinga Natural Reserve: a threatened Brazilian dry-forest with high biological value
Fig. 2. Rank-abundance (Log10 +1) of dung beetles species in two zones of the FLONA Contendas do SincorÁ management plan, Management zone (MZ) and Preservation zone (PZ). Numbers indicate the species ranked in both zones: 1. Canthon aff. piluliformes; 2. Canthon sp.1; 3. Uroxys sp.; 4. Dichotomius irinus; 5. Canthon aff. curvipes; 6. Deltochilum aff. calcaratum; 7. Ateuchus sp.; 8. Deltochilum verruciferum; 9. Dichotomius aff. semianeus; 10. Trichillum externepunctatum.
Fig. 1 in Dung beetles in a Caatinga Natural Reserve: a threatened Brazilian dry-forest with high biological value
Fig. 1. Sampled habitats of FLONA Contendas do SincorÁ, state of Bahia, Brazil during the dry season: a, Riparian Forest; b, Arboreal Caatinga; c, Capoeira.
Fig. 13 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 13. The tibia of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19030) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. Right tibia in anterior (A1) and posterior (A2) views, proximal end in lateral (A3) and proximal (A4) views. B. Femur-tibia articulation in posterior (B1) and anterior (B2) views.
Fig. 10 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 10. Fragmentary pterygoid and middle ear cavity of multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. A. IVPP V19025, middle ear with part of the promontorium in ventral view; photograph (A1), explanatory drawing (A2). B. IVPP V19029, possible bony shell of the inflated vestibule in lateral (B1) and inside (B2) views. The anterior end of each element is toward upside.
Fig. 3 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 3. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 (IVPP V19025) from the upper Paleocene Nomogen beds at the Erden (Urtyn) Obo locality, Inner Mongolia, China. Partial right rostrum with I2–3 in lateral (A) and ventral (B) views. A2, B2, explanatory drawings; A3, B3 details of A1, B1.
Fig. 2 in New specimens of the multituberculate mammal Sphenopsalis from China: Implications for phylogeny and biology of taeniolabidoids
Fig. 2. Multituberculate mammal Sphenopsalis nobilis Matthew, Granger, and Simpson, 1928 from the late Paleocene Gashato Formation at Shabarakh Usu, Mongolia. A. Holotype (AMNH 21736), the upper left M2 in occlusal, lingual and buccal views (A1–A3). B. Paratype (AMNH 21713), anterior part of a left m2 in occlusal view. C. Paratype (AMNH 21715), anterior parts of a left m1 in occlusal view. D. AMNH 21719.001, broken?M2 in occlusal ( D1) and lateral (D2) views. E. AMNH 21719.002, anterior parts of a left m1 in occlusal view.
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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.