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5,954 results for “Wasps”
Fig. 4 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey
Fig. 4. Phanacis ciceki sp. nov., ♀. a. Head in anterior view. b. Mesosoma in dorsal view. c. Metasoma in lateral view. d. Pronotum in dorsal view. e. Scutum in dorsal view. f. Scutellum in dorsal view.
Fig. 5 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey
Fig. 5. Phanacis ciceki sp. nov., ♀. a. Antenna. b. Head in dorsal view. c. Radial cell of forewing. d. Mesosoma in lateral view. e. Mesopleuron. f. Scutellum in lateral view.
Fig. 1 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey
Fig. 1. Aulacidea turguti sp. nov., ♀. a. Head in anterior view. b. Mesosoma in dorsal view. c. Metasoma in lateral view. d. Head in posterior view. e. Scutum in dorsal view. f. Scutellum in dorsal view.
Fig. 7 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey
Fig. 7. Phanacis urhani sp. nov., ♀. a. Head in anterior view. b. Mesosoma in dorsal view. c. Metasoma in lateral view. d. Head in dorsal view. e. Scutum in dorsal view. f. Scutellum in dorsal view.
Fig. 2 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey
Fig. 2. Aulacidea turguti sp. nov., ♀. a. Mesosoma in lateral view. b. Mesosoma in posterior view. c. Metasomal tergites T2, T3 and T4. d. Antenna. e. Leg. f. Radial cell of forewing.
Fig. 9 in Three new species of herb gall wasps (Hymenoptera: Cynipidae) from Turkey
Fig. 9. Phanacis urhani sp. nov., mature gall on host plant, Cirsium vulgare (Savi) Ten. (photos by M. Azmaz).
Figure 6–8 in A new species of Chrysobothris Eschscholtz (Coleoptera: Buprestidae) from nests of Cerceris fumipennis Say (Hymenoptera: Crabronidae) in northeastern Florida, USA, with new state records for species of Chrysobothris and a list of buprestid prey species taken by the wasp in Florida
Figure 6–8. Chrysobothris cerceripraeda Westcott and Thomas, n. sp. 6) Male aedeagus, dorsal. 7) Male aedeagus, ventral. 8) Female terminal ventrite.
Figures 1–5 in A new species of Chrysobothris Eschscholtz (Coleoptera: Buprestidae) from nests of Cerceris fumipennis Say (Hymenoptera: Crabronidae) in northeastern Florida, USA, with new state records for species of Chrysobothris and a list of buprestid prey species taken by the wasp in Florida
Figures 1–5. Chrysobothris cerceripraeda Westcott and Thomas, n. sp., male. 1) Dorsal habitus. 2) Front of head. 3) Ventral habitus. 4) Prosternum. 5) Protibia.
Figure 10–13. Locality photographs. 10 in A new species of Chrysobothris Eschscholtz (Coleoptera: Buprestidae) from nests of Cerceris fumipennis Say (Hymenoptera: Crabronidae) in northeastern Florida, USA, with new state records for species of Chrysobothris and a list of buprestid prey species taken by the wasp in Florida
Figure 10–13. Locality photographs. 10) View of salt marsh surrounding Pelotes Island Nature Preserve, Duval Co., FL. 11) Dirt road that runs length of Pelotes Island Nature Preserve. All Cerceris fumipennis Say nests were found on or next to road. 12) Drs. Leroy Whilby, FDACS-DPI CAPS, and Adam Silagyi, formerly FDACS-DPI CAPS, excavating nest of Cerceris fumipennis on Pelotes Island. 13) Excavation from nest of Cerceris fumipennis showing a common prey species, Chrysobothris shawnee Wellso and Manley.
Figure 2 in The natural history of the parasitic wasp Trogus pennator (Hymenoptera: Ichneumonidae): Host-finding behaviour and a possible host countermeasure
Figure 2. The frequency of plants damaged by Eurytides marcellus in the population was estimated at 16.4%. In contrast, 36% of the plants visited by the wasps were damaged (P,0.001, chi-square test).
Figure 3 in The natural history of the parasitic wasp Trogus pennator (Hymenoptera: Ichneumonidae): Host-finding behaviour and a possible host countermeasure
Figure 3. For those wasps (n533) that landed on and searched both undamaged Asimina plants and plants that were damaged by Eurytides marcellus, average searching times were significantly longer on damaged plants (P50.0016, two-tailed paired t test).
Figure 4 in The natural history of the parasitic wasp Trogus pennator (Hymenoptera: Ichneumonidae): Host-finding behaviour and a possible host countermeasure
Figure 4. The average height of plants searched by Trogus pennator (n557 wasps, range58–145 cm) and selected for oviposition by Eurytides marcellus (n541 butterflies, range52–95 cm) was compared in spring 1997. The wasps searched plants significantly taller than those preferred by the female butterflies (P,0.0001, two-tailed t test).
Figure 1. A in The natural history of the parasitic wasp Trogus pennator (Hymenoptera: Ichneumonidae): Host-finding behaviour and a possible host countermeasure
Figure 1. A vegetation survey was conducted in spring 1997 to establish the frequency of Asimina among the broad-leaved plants in the understorey. The mean percentage Asimina was determined at 7.5% by counting stems in 5 m×5 m plots. Plants counted as ''other'' most commonly included Quercus incana, Q. laevis, Vitis rotundifolia Micheaux, V. aestivalis Micheaux, Mimosa, sp., Smilax spp., and several unidentified Compositae. In contrast, 93.3% of plants visited by the wasps were Asimina (P,0.001, chi-square test).
Figures 11–16 in The parasitic wasp genera Skiapus, Hellwigia, Nonnus, Chriodes, and Klutiana (Hymenoptera, Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae
Figures 11–16. Scanning electron micrographs showing features of Skiapus sp. (Ophioninae). (11) Front of head showing emarginate eyes and twisted mandibles. (12) Back of head showing medially strongly excavated occiput and deflected occipital carina. (13) Metanotum and propodeum showing two complete transverse carinae located close to anterior margin. (14) Tibia of mid-leg, oblique angle, showing strong spines. (15) Hind coxa showing tooth near base. (16) Claw showing pectination.
Figure 4 in The parasitic wasp genera Skiapus, Hellwigia, Nonnus, Chriodes, and Klutiana (Hymenoptera, Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae
Figure 4. Partial alignments (arrangements) of four parts of the 28S D2 rDNA gene for representatives of the Campopleginae, Cremastinae, Ctenopelmatinae, and Ophioninae (aligned by eye) showing molecular synapomorphies for Campopleginae (1 and 2) and Ophioninae (3 and 4). Fragment 1 corresponds to bases 11– 24, fragment 2 to bases 47–62, fragment 3 to bases 203–225 (in box) and fragment 4 to bases 236 (in box) to 244 in the alignment shown in Belshaw et al. (1998, Figure 1).
Figure 1 in The parasitic wasp genera Skiapus, Hellwigia, Nonnus, Chriodes, and Klutiana (Hymenoptera, Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae
Figure 1. Strict consensus of: (a) MPTs with all characters unordered; (b) MPTs when selected characters treated as ordered; (c) after successive approximations weighting with selected characters treated as ordered.
Figure 3 in The parasitic wasp genera Skiapus, Hellwigia, Nonnus, Chriodes, and Klutiana (Hymenoptera, Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae
Figure 3. Strict consensus of trees obtained from simultaneous optimization alignment analyses of morphological and molecular data with gap:substitution ratio set at (a) 2:1, (b) 3:1, and (c) 4:1.
Figure 2 in The parasitic wasp genera Skiapus, Hellwigia, Nonnus, Chriodes, and Klutiana (Hymenoptera, Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae
Figure 2. Strict consensus of trees obtained from optimization alignment analysis of molecular data with gap:substitution ratio set at (a) 2:1, (b) 3:1, and (c) 4:1.
Figures 5–10 in The parasitic wasp genera Skiapus, Hellwigia, Nonnus, Chriodes, and Klutiana (Hymenoptera, Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae
Figures 5–10. Scanning electron micrographs showing features of Campopleginae sensu stricto and Nesomesochorinae stat. rev. (5) Echthronomas sp. (Campopleginae) hind tibia and basitarsus inner aspect showing unmodified tibial comb. (6–7, 9–10) Chriodes sp.: (6) hind tibia and basitarsus inner aspect showing modified tibial comb with medially reduced setae; (7) face; (9) claw showing pecten; (10) propodeum showing areolation. (8) Klutiana sp., face.
Figure 7 in Orb-web spiders (Araneae: Araneomorphae; Orbiculariae) captured by hunting-wasps (Hymenoptera: Sphecidae) in an area of Atlantic Forest in south-eastern Brazil
Figure 7. Eustala sp. 8 resting on vegetation. The spider remains holding a thread connected with the web hub. Scale bar: 1 cm.
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.