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403 results for “wasp parasite”
FIGURES 1–4. 1 in Notes on three braconid wasps (Hymenoptera: Braconidae, Doryctinae) parasitizing oak long-horned beetle, Massicus raddei (Coleoptera: Cerambycidae), a severe pest of Quercus spp. in China, together with the description of a new species
FIGURES 1–4. 1, Roburs (Quercus liaotungensis) damaged by Massicus raddei Blessig; 2, a single robur (Q. liaotungensis) damaged by M. raddei; 3, trunk of Q. liaotungensis with lots of exit holes produced by M. raddei; 4, cross section of tunnels bored by M. raddei.
FIGURES 27–31 in Notes on three braconid wasps (Hymenoptera: Braconidae, Doryctinae) parasitizing oak long-horned beetle, Massicus raddei (Coleoptera: Cerambycidae), a severe pest of Quercus spp. in China, together with the description of a new species
FIGURES 27–31. Zombrus bicolor (Enderlein), ♀. 27, Habitus; 28, head; 29, head and mesosoma; 30, mesosoma; 31, metasoma. 27, 29, 31, dorsal view; 28, frontal view; 30, lateral view.
FIGURES 9–14. Doryctes petiolatus Shestakov. 9, 13, 14 in Notes on three braconid wasps (Hymenoptera: Braconidae, Doryctinae) parasitizing oak long-horned beetle, Massicus raddei (Coleoptera: Cerambycidae), a severe pest of Quercus spp. in China, together with the description of a new species
FIGURES 9–14. Doryctes petiolatus Shestakov. 9, 13, 14, ♂; 10–12, ♀. 9, Habitus; 10, 11, head; 12, head and mesosoma; 13, mesosoma; 14, metasoma. 9, 10, 13, 14, dorsal view; 11, frontal view; 12, lateral view.
FIGURES 15–21 in Notes on three braconid wasps (Hymenoptera: Braconidae, Doryctinae) parasitizing oak long-horned beetle, Massicus raddei (Coleoptera: Cerambycidae), a severe pest of Quercus spp. in China, together with the description of a new species
FIGURES 15–21. Rhoptrocentrus quercusi sp.n., ♀. 15, 16, Habitus; 17, right antennae; 18, 19, head; 20, mesosoma; 21, metasoma. 15, 17, 19–21, dorsal view; 16, lateral view; 18, frontal view.
FIGURES 1–9 in New Agrilus Curtis (Coleoptera: Buprestidae) from México and Costa Rica mimicking parasitic wasps
FIGURES 1–9. Wasp-mimicking Agrilus: A. braconicoloratus Hespenheide, figures 1–2, dorsal and lateral views, figure 3, male genitalia; A. bellamyi New Species, figures 4–5, dorsal and lateral views; A. braconoides New Species, figures 6–7, dorsal and lateral views; and A. lucindae New Species, figures 8–9, dorsal and lateral views. Scale bars = 1 mm.
FIGURE 10 in New Agrilus Curtis (Coleoptera: Buprestidae) from México and Costa Rica mimicking parasitic wasps
FIGURE 10. Adult Agrilus bellamyi on leaf, type specimen, Michoacan, México; photograph by C.L. Bellamy.
FIGURE 10. Parasitic wasp Liris paralyzing a in New taxa and notes on crickets of the subfamily Landrevinae (Orthoptera: Gryllidae) from Brunei Darussalam, Borneo
FIGURE 10. Parasitic wasp Liris paralyzing a Landrevinae nymph (A); habitus of wasp in profile. Scale bar: 5 mm.
Figs 15–20 in Redescription of the parasitic wasp Melittobia sosui Dahms, 1984 (Hymenoptera: Eulophidae), with records on its new hosts in Vietnam
Figs 15–20. Melittobia sosui Dahms, male: 15 — head, frontal view; 16 — mandible; 17 — antenna, ventral view; 18 — mesosoma and metasoma, dorsal view; 19 — mid leg; 20 — habitus, lateral view. Рис. 15–20. Melittobia sosui Dahms, самец: 15 — голова, вид спереди; 16 — нижнЯЯ челюсть; 17 — антенна, вид сниЗу; 18 — меЗосома и метасома, вид сверху; 19 — среднЯЯ ножка; 20 — габитус, вид сбоку.
Data from: Parasitic wasps do not lack lipogenesis
<p>Fatty acids are crucial primary metabolites for virtually any creature on earth. Therefore, most organisms do not rely exclusively on nutritional supply with fatty acids but have the ability to synthesize fatty acids and triacylglycerides de novo from carbohydrates, a process called lipogenesis. The ubiquity of lipogenesis has been questioned by a series of studies reporting that many parasitic wasps (parasitoids) do not accumulate lipid mass despite having unlimited access to sugar. This has been interpreted as an evolutionary metabolic trait loss in parasitoids. Here, we demonstrate de novo biosynthesis of fatty acids from <sup>13</sup>C-labeled alpha-D-glucose in thirteen species of parasitoids from seven families. We furthermore show with the model organism <i>Nasonia vitripennis </i>that lipogenesis occurs even when lipid reserves are still intact, but relative <sup>13</sup>C-incorporation rates increase in females with widely depleted fat reserves. Therefore, we conclude that the presumed 'lack of lipogenesis' in parasitoids needs to be re-evaluated.</p>
Figure 37 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 37. (A) Strict consensus of 100 trees from analysis of characters treated as unordered (length = 145, RI = 0.618); (B) single successive approximations weighting tree from analysis of unordered characters (score = 79.96); (C) strict consensus of three trees from implied weighting analysis of unordered characters (score 25.964); (D) strict consensus of nine most parsimonious trees' characters all treated as ordered (length = 159, RI = 0.919); (E) single successive approximations weighting tree from analysis of ordered characters (score = 86.804); (F) strict consensus of three trees from implied weighting analysis of ordered characters (score 25.226).
Figure 36 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 36. Features of male tergal gland light micrographs. (A, B) Aleiodes (Hemigyroneuron) subscleroma, metasomal tergites 4 and 5 respectively, following maceration in potassium hydroxide and staining with chlorazol black, showing setae inside duct behind pore (arrows) and chitinous intima of large bilobed gland reservoir; (C) Aleiodes (Hemigyroneuron) dubiosus (Fullaway), posterior metasomal tergites showing peribasal concavities and specialised setal arrangement.
Figure 34 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 34. Aleiodes (Hemigyroneuron) ugandaensis sp. nov., CellD® light micrographs. (A) Habitus lateral aspect and associated mummified geometrid host remains; (B) head and mesosoma, dorsal aspect; (C) head, lateral aspect; (D) postero-ventral aspect of head showing occipital carina curving towards and joining hypostomal carina.
Figure 31 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 31. Aleiodes (Hemigyroneuron) suffusus (Baker), CellD® light micrographs. (A) Lateral habitus; (B) head, dorsal aspect; (C) head, frontal aspect; (D) mesosoma, lateral aspect; (E) metasomal tergites 2 and 3.
Figure 33 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 33. Aleiodes (Hemigyroneuron) trianguliscleroma sp. nov., CellD® light micrographs. (A) Habitus, lateral aspect; (B) head, frontal aspect; (C) wing features showing modified subbasal cell and straight vein 1-SR+M of fore wing, and hind wing with trace of vein m-cu; (D) head, dorsal aspect; (E) metasomal tergites 1–3.
Figure 32 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 32. Aleiodes (Hemigyroneuron) suffusus (Baker), CellD ® light micrographs. (A) detail of fore wing venation showing lack of sclerome (small dark spot is a speck of dirt); (B) detail of hind wing showing large cu-a bulla, short vein 1-M relative to M+CU, and transverse vein 2-SC+R.
Figure 30 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 30. Aleiodes (Hemigyroneuron) speciosus (Baker), CellD® light micrographs. (A) Remaining part of fore wing; (B) hind wing venation.
Figure 28 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 28. Aleiodes (Hemigyroneuron) sharkeyi sp. nov., CellD ® light micrographs. (A) Lateral habitus; (B) head, dorsal aspect; (C) detail of fore wing venation; (D) head, frontal aspect; (E) mesosoma, dorsal aspect.
Figure 27 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 27. Aleiodes (Hemigyroneuron) roberti sp. nov., CellD® light micrographs. (A) Metasoma, dorsal aspect; (B) metasomal tergites 4–6, detail showing pore openings (arrows) and internal glandular ducts visible through cuticle.
Figure 23 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 23. Aleiodes (Hemigyroneuron) pseudospeciosus sp. nov., CellD ® light micrographs. (A) Lateral habitus; (B) head, frontal aspect; (C) head, dorsal aspect; (D) metasomal tergites 1–3.
Figure 25 in Revision of Aleiodes (Hemigyroneuron) parasitic wasps (Hymenoptera: Braconidae: Rogadinae) with reappraisal of subgeneric limits, descriptions of new species and phylogenetic analysis
Figure 25. Aleiodes (Hemigyroneuron) roberti sp. nov., CellD® light micrographs. (A) Lateral habitus; (B) head, frontal aspect; (C) head, dorsal aspect; (D) mesoscutum, dorsal aspect; (E) head and pronotum, lateral aspect.
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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)
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.