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171 results for “Orchid bees”
FIGURE 1 in Orchid Bees (Hymenoptera: Apidae) In The Coastal Forests Of Southern Brazil: Diversity, Efficiency Of Sampling Methods And Comparison With Other Atlantic Forest Surveys
FIGURE 1: DCA analysis of the orchid bee assemblages along the Brazilian Atlantic forest (see text for site codes; the two sites from the current study, PR3 and SP3, are shown in gray).
Figure 1. Baited trap made with 500 in Is the capture success of orchid bees %Hymenoptera, Apoidea) influenced by different baited trap designs? A case study from southern Brazil
Figure 1. Baited trap made with 500 mL bottle; left landing platform not shown to indicate position of the entrance hole.
Figure 4 in Orchid bees (Apidae: Euglossini) in Cerrado remnants in northeast Brazil
Figure 4. Influence of temperature on the patterns of daily activity of the five most abundant species in gallery forest (a) and Cerrado sensu stricto (b) of the Mirador State Park, MA.
Figure 1 in Orchid bees (Apidae: Euglossini) in Cerrado remnants in northeast Brazil
Figure 1. Distribution of the Cerrado biome in Brazil and Maranhão (grey area). Dark area represents the geographic location of Mirador State Park, MA, and the points correspond to study areas in gallery forest (GF) and Cerrado sensu stricto (Css) (QGIS Software 2.18, Quantum GIS Development Team2017).
Figure 3 in Orchid bees (Apidae: Euglossini) in Cerrado remnants in northeast Brazil
Figure 3. Distribution of the most abundant Euglossini species during 18 months of sampling, and monthly mean temperature and humidity in two areas of the Cerrado biome in Mirador State Park, MA: gallery forest (a) and Cerrado sensu stricto (b).
Figure 1 in Foraging patterns and artificial fragrance choices of male orchid bees in the Brazilian Atlantic Rainforest
Figure 1. Number of male euglossine bees belonging to the four most abundant species of orchid bees (Euglossa annectans, E. stellfeldi, E. iopoecila and E. roderici) attracted monthly to the eight fragrances offered to bees during the wet-warm season: (a) on Superagui Island (SI), over three sampling periods; (b) on RNSM. O, N, D, J, F, M, A = October, November, December, January, February, March and April, respectively. EG = eugenol; EC = eucalyptol; VN = vanillin; BI = betaionone; BA = benzyl acetate; MS = methyl salicylate; BB = benzyl benzoate; MC = methyl cinnamate.
Figure 1 in Time-lapse photography reveals the occurrence of unexpected bee-pollination in Calanthe izuinsularis, an endangered orchid endemic to the Izu archipelago
Figure 1. Flowers and insect visitors of Calanthe izuinsularis. (a) Photoscotosia lucicolens; (b) Odontopera arida melanchonica; (c) Noctuidae sp.; (d) Geometridae sp.; (e) Trichoplusia intermixta; (f) Diarsia deparca; (g) Paliga minnehaha; (h) Serrodes campanus; (i) Lasioglossum apristum; (j) Lasioglossum occidens; (k) Lasioglossum occidens. The pollinaria indicated by white arrows can be seen attached to the bee's mesothorax.
Figure 1 in Using short-term surveys and mark-recapture to estimate diversity and population size of orchid bees in forest formations of the Brazilian savanna
Figure 1. Marking method used in the study of euglossine populations. (a) During all populational estimatives. Each geometric shape corresponds to the day when the PTT was collected. Square = 1st day; circle = 2nd day; pentagon = 3rd day; triangle = 4th day; diamond = 5th day. (b) During the samplings occurred simultaneously in seasonal semi-deciduous (ssf) and gallery forest (ssf). Square = 1st day; circle = 2nd day; pentagon = 3rd day; square combined with spot on the wing = 4th day; circle combined with spot on the wing = 5th day.
Figure 2 in Orchid bees (Hymenoptera, Apidae, Euglossini) are seasonal in Seasonal Semideciduous Forest fragments, southern Brazil
Figure 2. Orchid bee phenology in Seasonal Semideciduous Forest fragments, Euglossa fimbriata.
FIGURE 1 in The orchid-bee fauna (Hymenoptera: Apidae) of a forest remnant in southern Bahia, Brazil, with new geographic records and an identification key to the known species of the area
FIGURE 1. Map showing the exact location of Parque Estadual da Serra do Conduru, state of Bahia, Brazil. Approximate location of Estação Veracel in southern Bahia is indicated by the orange square.
FIGURE 2 in Euglossa (Glossura) bazinga sp. n. (Hymenoptera: Apidae: Apinae, Apini, Euglossina), a new orchid bee from western Brazil, and designation of a lectotype for Euglossa (Glossura) ignita Smith, 1874
FIGURE 2. Comparing holotype Euglossa bazinga sp. n. (left column) to E. ignita Smith, 1874 (right column): A–B: dorsal view of metasoma; C–D: frontal view of face; E–F: ventral view of mesotibia; G–H: metatibia. Figures 2B, D, F and H from an E. ignita specimen from the Amazon (see Appendix 1).
FIGURE 3 in Euglossa (Glossura) bazinga sp. n. (Hymenoptera: Apidae: Apinae, Apini, Euglossina), a new orchid bee from western Brazil, and designation of a lectotype for Euglossa (Glossura) ignita Smith, 1874
FIGURE 3. Comparing Euglossa bazinga sp. n. (left column) to E. ignita Smith, 1874 (right column): A–B: ventral view of metasoma focusing on S2; C–D: dorsal view of left S2 pocket (setae were removed); E–F: frontal view of left S2 pocket (setae were removed)—see Diagnosis for discussion. Figure 3A from the holotype; Figure 3C and 3E from a paratype. Figures 3B, D and F from an E. ignita specimen from the Amazon (see Appendix 1).
FIGURE 4 in Euglossa (Glossura) bazinga sp. n. (Hymenoptera: Apidae: Apinae, Apini, Euglossina), a new orchid bee from western Brazil, and designation of a lectotype for Euglossa (Glossura) ignita Smith, 1874
FIGURE 4. Comparing Euglossa bazinga sp. n. (left column) to E. ignita Smith, 1874 (right column): A–B: seventh sternum; C–D: eighth sternum; E–F: lateral view of genital capsule; D–F: dorsal view of genital capsule.
FIGURE 1 in Euglossa (Glossura) bazinga sp. n. (Hymenoptera: Apidae: Apinae, Apini, Euglossina), a new orchid bee from western Brazil, and designation of a lectotype for Euglossa (Glossura) ignita Smith, 1874
FIGURE 1. Map illustrating the localities where Euglossa bazinga sp. n. was recorded. Ligth grey shadows = Cerrado (savannah-like vegetation); dark grey = Atlantic Forest.
Data from: Conservation genetics of Neotropical pollinators revisited: microsatellite analysis suggests that diploid males are rare in orchid bees
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The evolution of sexual signaling is linked to odorant receptor tuning in perfume-collecting orchid bees
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Data from: Climate, physiological tolerance, and sex-biased dispersal shape genetic structure of Neotropical orchid bees
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Figure 4 from: Galgani-Barraza P, Moreno JE, Lobo S, Tribaldos W, Roubik DW, Wcislo WT (2019) Flower use by late nineteenth-century orchid bees (Eufriesea surinamensis, Hymenoptera, Apidae) nesting in the Catedral Basílica Santa María la Antigua de Panamá. Journal of Hymenoptera Research 74: 65-81. https://doi.org/10.3897/jhr.74.39191
Figure 4 Eufriesea surinamensis cells painted during the nineteenth-century restoration A close-up of a cell cluster recovered from a capital B isolated cell entrance that was painted over C isolated cell entrance showing the abundance of bark fragments as a main resource for nest construction D cell cluster covered in golden paint E exterior view of an isolated cell, covered with golden leaf; the cell entrance faces right.
Figure 2 from: Galgani-Barraza P, Moreno JE, Lobo S, Tribaldos W, Roubik DW, Wcislo WT (2019) Flower use by late nineteenth-century orchid bees (Eufriesea surinamensis, Hymenoptera, Apidae) nesting in the Catedral Basílica Santa María la Antigua de Panamá. Journal of Hymenoptera Research 74: 65-81. https://doi.org/10.3897/jhr.74.39191
Figure 2 Panama City's waterfront and surrounding area as seen from the shoreline of Casco Viejo, Panamá in 1875. The large building in the left foreground is La Casa de la Marina, near El Palacio de las Garzas (Presidential Palace). The bees were nesting approximately 160 m in-land. The peak of Cerro Ancón is approximately 1.6 km distant. Photo by Eadweard Muybridge, courtesy of the Smithsonian American Art Museum; gift of Mitchell and Nancy Steir.
Figure 3 from: Galgani-Barraza P, Moreno JE, Lobo S, Tribaldos W, Roubik DW, Wcislo WT (2019) Flower use by late nineteenth-century orchid bees (Eufriesea surinamensis, Hymenoptera, Apidae) nesting in the Catedral Basílica Santa María la Antigua de Panamá. Journal of Hymenoptera Research 74: 65-81. https://doi.org/10.3897/jhr.74.39191
Figure 3 Locations of nest cell aggregations of Eufriesea surinamensis within the Cathedral in Casco Viejo, Panamá A restored reredos showing the capitals above the columns where the historical bee cells were found (black arrows) B a scroll removed during the contemporary restoration, showing bee cells within its crevices and golden material applied during the nineteenth-century restoration C close-up of scrolls on a capital showing painted bee cells from the prior restoration.
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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.