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171 results for “Orchid bees”
Figures 3–9 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 3–9. Euglossa (Euglossella) viridis (Perty), male. 3. Facial aspect. 4. Mesotibial tufts. 5. Outer view of hind leg. 6. Lateral part of mesepisternum. 7. Mesoscutellum. 8. Proximal section of mesobasitarsus. 9. Dorsal view of metasomal terga.
Figures 96–104 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 96–104. Euglossa (Euglossella) cyanura Cockerell. 96. Facial aspect of male. 97. Facial aspect of female. 98. Mesotibial tufts of male. 99. Outer view of male hind leg. 100. Proximal section of male mesobasitarsus. 101. Outer view of female hind leg. 102. Anterolateral view of mesepisternum of male. 103. Mesoscutellum of male. 104. Dorsal view of male metasomal terga.
Figures 139–140 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 139–140. Euglossa (Euglossella) perfulgens Moure, female. 139. Dorsal habitus. 140. Lateral habitus.
Figures 109–116 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 109–116. Euglossa (Euglossella) granti Cheesman. 109. Facial aspect of male. 110. Facial aspect of female holotype. 111. Mesotibial tufts of male. 112. Proximal section of male mesobasitarsus. 113. Outer view of male hind leg. 114. Outer view of metabasitarsus of female holotype. 115. Mesoscutellum of male. 116. Dorsal view of male metasomal terga.
Figures 94–95 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 94–95. Euglossa (Euglossella) cyanura Cockerell, female. 94. Dorsal habitus. 95. Lateral habitus.
Figures 107–108 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 107–108. Euglossa (Euglossella) granti Cheesman, female holotype. 107. Dorsal habitus. 108. Lateral habitus.
Figures 88–89 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 88–89. Euglossa (Euglossella) ashei, new species, female holotype. 88. Dorsal habitus. 89. Lateral habitus.
Figures 144–154 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 144–154. Outer view of mesotibiae of males of species of Euglossella Moure, viridis and mandibularis species groups. 144. Euglossa (Euglossella) viridis (Perty). 145. E. (E.) azurea Ducke. 146. E. (E.) celiae, new species. 147. E. (E.) cyanea Friese. 148. E. (E.) subandina, new species. 149. E. (E.) polita Ducke. 150. E. (E.) perviridis Dressler. 151. E. (E.) cyanura Cockerell. 152. E. (E.) granti Cheesman. 153. E. (E.) mandibularis Friese. 154. E. (E.) bigibba Dressler.
Fig. 2 in A New Fossil Orchid Bee in Colombian Copal (Hymenoptera: Apidae)
Fig. 2. Metatibia of Euglossa (Euglossa) cotylisca Hinojosa-Díaz and Engel, new species (NHML Pal. PI II
Fig. 1 in A New Fossil Orchid Bee in Colombian Copal (Hymenoptera: Apidae)
Fig. 1. Photomicrograph of Euglossa (Euglossa) cotylisca Hinojosa-Díaz and Engel, new species (NHML Pal. PI II 670 [1]) in Colombian copal; above, a view of the entire piece encapsulating the bee; below, dorsal aspect of the bee in detail. [Upper image by I.A.H.-D., 2006; lower image by P.V. York, reproduced with permission of the NHML, º The Natural History Museum, London].
Fig. 1 in Orchid bees (Hymenoptera: Apidae: Euglossini) of Cusuco National Park, State of Cortés, Honduras
Fig. 1. (a) Location of Cusuco National Park and (b) locations of research camps within the park.
Figures 38–39 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 38–39. Euglossa (Euglossella) cyanea Friese, male. 38. Dorsal habitus. 39. Lateral habitus.
Figures 60–61 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 60–61. Euglossa (Euglossella) polita Ducke, male. 60. Dorsal habitus. 61. Lateral habitus.
Figures 16–17 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 16–17. Euglossa (Euglossella) azurea Ducke, male. 16. Dorsal habitus. 17. Lateral habitus.
Figures 1–2 in Revision of the orchid bee subgenus Euglossella (Hymenoptera: Apidae), Part II: The viridis and mandibularis species groups
Figures 1–2. Euglossa (Euglossella) viridis (Perty), male. 1. Dorsal habitus. 2. Lateral habitus.
Figure 1 in Orchid bees (Hymenoptera, Apidae, Euglossini) are seasonal in Seasonal Semideciduous Forest fragments, southern Brazil
Figure 1. Orchid bee phenology in Seasonal Semideciduous Forest fragments, (A-C) Eufriesea violacea, (D-G) Euglossa cordata, (H-I) Eulaema nigrita.
Phylogenomics reveals within species diversification but incongruence with color phenotypes in widespread orchid bees (Hymenoptera: Apidae: Euglossini)
<p>Coloration is an important phenotypic trait for taxonomic studies and has been widely used for identifying insect species and populations. However, coloration can be a poor diagnostic character for insect species that exhibit high polymorphism in this trait, which can lead to over-splitting of taxonomic units. In orchid bees, color variation has been interpreted by different taxonomists as either polymorphism associated with Mullerian mimicry complexes or diagnostic traits for species identification. Despite this uncertainty, integrative approaches that incorporate multiple independent datasets to test the validity of hair coloration as a character that identifies independent evolutionary units have not been used. Here, we use phylogenomic data from Ultraconserved Elements (UCEs) to explore whether color phenotypes in the widespread orchid bee species complexes <em>Eulaema</em> <em>meriana</em> and <em>Eulaema</em> <em>bombiformis</em> (Hymenoptera: Apidae: Euglossini) correspond to independent lineages or polymorphic trait variation within species. We find that lineages within both species are structured according to geography and that color morphs are generally unassociated with evolutionarily independent groups except for populations located in the Atlantic Forest of Brazil. We conclude that there is compelling evidence that <em>E. atleticana </em>and <em>E. niveofasciata</em> are subspecies of <em>E. meriana</em> and <em>E. bombiformis</em>, respectively, and not different species as previously suggested. Therefore, we recognize <em>Eulaema meriana atleticana</em> comb. n. and <em>Eulaema bombiformis niveofasciata</em> comb. n. and discuss their morphological characteristics. We make recommendations on the use of color traits for orchid bee taxonomy and discuss the significance of subspecies as evolutionary units relevant for conservation efforts.</p>
Experimental disruption of social structure reveals totipotency in the orchid bee, Euglossa dilemma
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Data from: Macroevolution of perfume signalling in orchid bees
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Phylogenomics reveals within species diversification but incongruence with color phenotypes in widespread orchid bees (Hymenoptera: Apidae: Euglossini)
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Allen Brain Atlas
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OpenNeuro
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