Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
769
datasets available to search
ShareScore release 0.9.0
Dataset results
769 results for “orchids,”
FIGURE 4 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters
FIGURE 4. Holotype Eufriesea zhangi sp. n. A: dorsal view of head and mesosoma; B: frontal view of face; C: dorsal view of metasoma; D: ventral view of mesotiba. E: frontal view of metatibia; F: metatibia seen from above.
FIGURE 2 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters
FIGURE 2. Cluster of the 35 specimens (numbers 2 to 36) of Eufriesea nordestina (Moure, 1999) and the single specimen of Eufriesea zanghi sp. n. (number 1, right side) according to measurements of four morphological characters through SAS (see 'Material and Methods'). Each specimen is represented by numbers 1 to 36. The correspondent identification and access number at UFMG collection is shown in Appendix 1.
FIGURE 1 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters
FIGURE 1. Map illustrating northeastern Brazil and the type locality (black square) of Eufriesea zhangi sp. n. Acronyms represent Brazilian states, as following: AL: Alagoas; BA: Bahia; CE: Ceará; PB: Paraíba; PE: Pernambuco; PI: Piauí; RN: Rio Grande do Norte; SE: Sergipe.
FIGURE 3 in Eufriesea zhangi sp. n. (Hymenoptera: Apidae: Euglossina), a new orchid bee from Brazil revealed by molecular and morphological characters
FIGURE 3. Tree constructed from the COI gene sequences using Maximum Likelihood (ML). An identical topology was obtained with Maximum Parsimony (MP), and bootstrap values for both reconstruction methods are shown above (ML) and below (MP) branches. The numbers shown in parentheses after the taxon names refer to the lineages and locations presented in Table 2. Exaerete smaragdina (Guérin-Méneville, 1844) was used as outgroup.
Fig. 6 in Beetles with Orchid Pollinaria in Dominican and Mexican Amber
Fig. 6. Detail of annulated pollinia of Annulites mexicana gen. n., sp. n. Scale = 0.9 mm. Insert shows pollen tetrads (arrow) between segments. Scale = 80 µm.
Fig. 7 in Beetles with Orchid Pollinaria in Dominican and Mexican Amber
Fig. 7. Outlines of pollinaria of Cylindrocites browni gen. n., sp. n. (A) and Annulites mexicana gen. n., sp. n. (B). Arrows show viscidia.
Fig. 3 in Beetles with Orchid Pollinaria in Dominican and Mexican Amber
Fig. 3. Lateral view of pollinarium of Cylindrocites browni gen. n., sp. n. attached to weevil. V= viscidium. Top arrow shows mucoid connection between viscidium and weevil. Bar = 0.4 mm. Insert shows pollen tetrads (arrow) inside pollinium. Scale = 60 µm.
Fig. 1 in Beetles with Orchid Pollinaria in Dominican and Mexican Amber
Fig. 1. Dominican amber cryptorhynchid weevil with attached pollinarium (arrow) of Cylindrocites browni gen. n., sp. n. Floral remains in background. Scale = 3.0 mm.
Fig. 4 in Beetles with Orchid Pollinaria in Dominican and Mexican Amber
Fig. 4. Mexican amber ptilodactyline beetle with attached pollinium of Annulites mexicana gen. n., sp. n. (arrow). Scale = 0.4 mm.
Fig. 5 in Beetles with Orchid Pollinaria in Dominican and Mexican Amber
Fig. 5. Pollinium (arrow) of Annulites mexicana gen. n., sp. n. attached to the mouthparts of a ptilodactyline beetle in Mexican amber. Scale = 0.3 mm.
FIGURE 1 in Euglossa bembei sp. n. (Hymenoptera: Apidae): a new orchid bee from the Brazilian Atlantic Forest belonging to the Euglossa cybelia Moure, 1968 species group
FIGURE 1. Holotype male Euglossa bembei sp. n. (left column) and male Euglossa ioprosopa Dressler, 1982 (right column). A: dorsal view of E. bembei sp. n. B: dorsal view of E. ioprosopa. C: frontal view of face of E. bembei sp. n. D: frontal view of face of E. ioprosopa. E: mesotibia of E. bembei sp. n. F: mesotibia of E. ioprosopa. G: ventral view of metasoma of E. bembei sp. n. H: ventral view of metasoma of E. ioprosopa.
FIGURE 2 in Euglossa marianae sp. n. (Hymenoptera: Apidae): a new orchid bee from the Brazilian Atlantic Forest and the possible first documented local extinction of a forest-dependent orchid bee
FIGURE 2. Holotype Euglossa marianae sp. n. A: dorsal view. B: frontal view of face. C: last three terga. D: metatibia. E: mesotibia. F: mesotibia of one specimen of Euglossa analis from Parque Nacional da Serra do Divisor, state of Acre, Brazilian Amazon (specimen number 12417-36556, deposited at UFMG).
FIGURE 1 in Euglossa marianae sp. n. (Hymenoptera: Apidae): a new orchid bee from the Brazilian Atlantic Forest and the possible first documented local extinction of a forest-dependent orchid bee
FIGURE 1. Map showing the location of the three areas sampled in this study (yellow circles), the type locality of Euglossa marianae sp. n. (green circle), and the known areas where this species has been recorded (red circles) (see text for details).
FIGURE 1 in The orchid-bee fauna (Hymenoptera: Apidae) of a forest remnant in northeastern Brazil, with new geographic records and an identification key to the known species of the Atlantic Forest of northeastern Brazil
FIGURE 1. Map showing the Estação Ecológica de Murici, Murici, state of Alagoas. The red line defines the limits of the ecological station. Numbers 1, 2, and 3 refers to the sites 1, 2, and 3 (see Material and Methods).
Figure 3 in New species of Megastylus (Hymenoptera: Ichneumonidae: Orthocentrinae) reared from larvae of Keroplatidae fungus gnats (Diptera) in a Dutch orchid greenhouse
Figure 3. (a) Keroplatid larva parasitized by Megastylus woelkei sp. nov.ι inside the keroplatid larva the larva of M. woelkei is visible; (b) cocoon of M. woelkei sp. nov. from which the adult wasp has already emergedι scale bar 1.0 mm; (c) keroplatid pupa from orchid nurseryι scale bar 1.0 mm; (d) female of Lyprauta cambriaι one of the three probable host species for M. woelkei sp. nov.ι scale bar 1.0 mm.
Figure 2 in New species of Megastylus (Hymenoptera: Ichneumonidae: Orthocentrinae) reared from larvae of Keroplatidae fungus gnats (Diptera) in a Dutch orchid greenhouse
Figure 2. Megastylus woelkei sp. nov.ι paratype male: (a) whole insectι scale bar 0.5 mm; (b–d) variation of face colour (anterior view)ι scale bar 0.2 mm; (e) head (dorsal view)ι scale bar 0.2 mm; (f) parameres (lateral view)ι scale bar 0.2 mm.
Figure 1 in New species of Megastylus (Hymenoptera: Ichneumonidae: Orthocentrinae) reared from larvae of Keroplatidae fungus gnats (Diptera) in a Dutch orchid greenhouse
Figure 1. Megastylus woelkei sp. nov.ι holotype female: (a) whole insectι scale bar 0.5 mm; (b) head (anterior view)ι scale bar 0.2 mm; (c) head and mesosoma (latero-ventral view)ι scale bar 0.5 mm; (d) head (dorsal view)ι scale bar 0.2 mm; (e) propodeum and tergites 1–5 of metasoma (dorsal view)ι scale bar 0.5 mm; (f) wingsι scale bar 0.5 mm.
FIGURES 1–8 in The male gonostylus of the orchid bee genus Euglossa (Apidae: Euglossini)
FIGURES 1–8. Male genital structures of the orchid bee genus Euglossa. 1 = Genital capsule of Euglossa sp. in dorsal (left) and ventral (right) views. 2–8, types of gonostyli (I–V) recognized herein; gonostyli represented in drawing lines were removed from genital capsules and flattened on a microscope slide (see text for explanation). 2 = Type I, E. (Euglossa) ioprosopa; 3 = Type II, E. (Glossurella) prasina; 4–6 = Type III, E. (Euglossa) cognata, E. (Euglossella) cyanura and E. (Euglossa) modestior respectively; 7 = Type IV, E. (Euglossa) championi; 8 = Type V, E. (Glossurella) fuscifrons.
Figure 7 in Characterization of the orchid bee Euglossa viridissima (Apidae: Euglossini) and a novel cryptic sibling species, by morphological, chemical, and genetic characters
Figure 7. Geographical distribution of tridentate Euglossa dilemma sp. nov. (black) and predominantly bidentate Euglossa viridissima (white) as inferred from recent baiting assays (circles) as well as museum material (diamonds). Note lack of E. viridissima in the south-eastern part (Costa Rica) of the range. Museum material included paratypes of E. dilemma and additional specimens of one or both species in the collections of D. W. Roubik, T. Eltz (CTE), G. Gerlach (CGG), the Zoologische Staatssammlung München (ZSM), the Smithsonian Institution (SI), and the Snow Entomological Collection (SEC). Only unambiguous and non-redundant localities were plotted. Localities of baiting assays are (from west to east): Chamela (Jalisco, Mexico), El Chote (Veracruz, Mexico), Ayozinthepec (Oaxaca, Mexico), Monte Pio and Poza Azul (both Veracruz, Mexico), Tuxtla Gutiérrez, Esquintla, Tapachula, Ocosingo and Palenque (all Chiapas, Mexico), Atasta (Campeche, Mexico), Retalhuleu (Guatemala), Lacanjá (Chiapas, Mexico), Escarcega (Campeche, Mexico), El Remate (Campeche, Mexico), Chablekal, Xmatkuil (Yucatán, Mexico), Tikal (Guatemala), San Crisanto (Yucatán, Mexico), Chetumal and Coba (both Quintana Roo, Mexico), Chinandega, Chacocente, Escameca Grande, Jinotega, Ometepe and Las Pampas (all Nicaragua), and Area de Conservación Guanacaste (Costa Rica).
Figure 6 in Characterization of the orchid bee Euglossa viridissima (Apidae: Euglossini) and a novel cryptic sibling species, by morphological, chemical, and genetic characters
Figure 6. Chronogram showing divergence times and phylogenetic relationships of selected lineages in the genus Euglossa and the sibling species Euglossa dilemma sp. nov. and E. viridissima. The tree topology corresponds to that obtained via Bayesian methods. Bayesian posterior probabilities and parsimony bootstrap values are shown for the sister species only. Divergence times were obtained via penalized likelihood using the fossil-calibrated molecular clock procedures described in Ramírez et al. (2010b). The maximum and minimum age estimates for the MRCA of E. dilemma and E. viridissima correspond to the molecular clock analyses in which the MRCA of the genus Euglossa was assigned a fossil calibration of 20 and 15 Myr, respectively.
ScienceDex guides
Understand access before you commit
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.