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1,108 results for “Parasitoid wasps”
Figure 25. Consecutive frames from a in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 25. Consecutive frames from a video (29.80 fps) of a male M. exasperans displaying to a nearby male of the same species. In 0.30s 2.5 cycles of back and forth movement of legs I (~8° amplitude, ~8.3 cycles/s) was observed.
Figure 5 in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 5. Detailed views of a dried adult male Myrmarachne exasperans (not living). 2-3, Dorsal view of chelicerae with fangs retracted (2) and extended (3). 4-6, Ventral views of chelicerae in different positions. Note the posterior (ventral) position of the fang groove (6, arrow), lined with short spines along the rear margin. 7, Prolateral or anterior view of right leg I showing six long spines of each tibia and two long spines of each metatarsus. These spines are very thin and sharp. 8, Detail of distal tarsus and pretarsus from (7), showing closely spaced teeth of the anterior claw.
Figure 21. Sequential frames from a in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 21. Sequential frames from a video (29.79 fps) of a moving adult female Myrmarachne exasperans. Up and down (bobbing) movement of the opisthosoma relative to each preceding frame is indicated with arrows. Maximum recorded rates of movement were ~15 cycles/s (e.g., between frames [1] and [4]), with 10 cycles completed in this 0.97s sequence for an average, including interruptions, of 10.3 cycles/s.
Figure 10 in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 10. Detailed views of an adult female Myrmarachne exasperans. 1, The anterodorsal carapace of the female has the same iridescent violet color as the male chelicerae. 4, Detail of inset from (3), showing the elongated, fringed scales that comprise the distinctive markings of the dorsal opisthosoma. 5, The flattened pedipalps of the female are mostly glabrous dorsally, fringed with stout, sharply pointed setae (arrows). 6-9, Ventral (6) to dorsal (9) composite images of dried left pedipalp of female, showing stout ventral and marginal setae and relatively smooth dorsal plate (9). Distally (toward the top of the page) there appears to be a small tuft of more flexible, light-colored spondylae (whorled or chemosensory setae).
Figure 9 in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 9. Detailed views of an adult female Myrmarachne exasperans. 1, The anterodorsal carapace of the female has the same iridescent violet color as the male chelicerae. 4, Detail of inset from (3), showing the elongated, fringed scales that comprise the distinctive markings of the dorsal opisthosoma.
Figure 8 in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 8. Detailed views of the prosoma of an adult female Myrmarachne exasperans. Note the array of short, papillate setae between the posterior eyes (5), and the rugose texture of the sides of the posterior middorsal crest of the carapace (6).
Figure 26. Consecutive frames from a in Notes on the jumping spider Myrmarachne exasperans (Araneae: Salticidae: Astioida: Myrmarachnini) in Bali, a possible mimic of parasitoid wasps (Hymenoptera: Ichneumonidae: Cryptini: Goryphus)
Figure 26. Consecutive frames from a video (29.81 fps) of a male M. exasperans displaying to a nearby male of the same species. In 0.30s 3.0 cycles of back and forth movement of legs I (~8° amplitude, ~10.0 cycles/s) was observed.
Figure 4 in New records and a voucher collection of parasitoid wasps (Hymenoptera) inhabiting agroforestry systems in the colombian amazon basin
Figure 4. Habitus of Chalcidoidea collected in agroforestry systems of cacao (Theobroma cacao) and copoazu (T. grandiflorum). (A) Haltichella hydara (Walker, 1842) [UNAB 1190], (B) Stypiura sp. [UNAB 1356], (C) Aenasius sp. (Encyrtidae) [UNAB 663], (D) Coelopencyrtus sp. [UNAB 2538], (E) Horismenus striatus Hansson, 2009 (Eulophidae) [UNAB 1196], (F) Brasema sp. (Eupelmidae) [UNAB 1358], (G) Anastatus sp. (Eupelmidae) [UNAB 1192], (H) Neorileya flavipes Ashmead, 1904 (Eurytomidae) [UNAB 1432], (I) Perilampus sp. (Perilampidae) [UNAB 1361], (J) Erotolepsia sp. (Pteromalidae) [UNAB 661], (K) Bubekia tricarinata (Ashmead, 1888) (Pteromalidae) [UNAB 3464], (L) Lelaps affinis Ashmead, 1904 (Pteromalidae) [UNAB 658].
Figure 3 in New records and a voucher collection of parasitoid wasps (Hymenoptera) inhabiting agroforestry systems in the colombian amazon basin
Figure 3. Habitus of parasitoid wasps collected in agroforestry systems of cacao (Theobroma cacao) and copoazu (T. grandiflorum). (A) Aclista sp. (Diapriidae) [UNAB 3747], (B) Basalys sp. (Diapriidae) [UNAB 1198], (C) Paramesius sp. (Diapriidae) [UNAB 1194], (D) Trichoplasta sp. (Figitidae) [UNAB 1423], (E) Aganaspis sp. (Figitidae) [UNAB 1464], (F) Tropideucoila sp. (Figitidae) [UNAB 1422].
Figure 2 in New records and a voucher collection of parasitoid wasps (Hymenoptera) inhabiting agroforestry systems in the colombian amazon basin
Figure 2. Bar charts of parasitoid wasp families and genera of collected individuals inhabiting agroforestry systems of cacao (Theobroma cacao) and copoazu (T. grandiflorum) from the Colombian Amazon basin. (A) number of individuals per family, (B) number of genera and species per family.
Figure 5 in New records and a voucher collection of parasitoid wasps (Hymenoptera) inhabiting agroforestry systems in the colombian amazon basin
Figure 5. Habitus of Platygastroidea (Scelionidae) collected in agroforestry systems of cacao (Theobroma cacao) and copoazu (T. grandiflorum). (A) Apegus sp. [UNAB 1445], (B) Calliscelio sp. [UNAB 1439], (C) Gryon sp. [UNAB 1442], (D) Scelio sp. [UNAB 1438], (E) Xenomerus sp. [UNAB 1443], (F) Thoron sp. [UNAB 3765].
Figure 17 in Comparative morphology, biology and phylogeny of terminal-instar larvae of the European species of Toryminae (Hym., Chalcidoidea, Torymidae) parasitoids of gall wasps (Hym. Cynipidae)
Figure 17. Tree from heuristic search of phylogenetic analyses of larval data.
Figure 3 in Inferring life history from ovipositor morphology in parasitoid wasps using phylogenetic regression and discriminant analysis
Figure 3. Measurements used in the analyses. See Table 3 for further explanation of characters.
Delimiting the cryptic diversity and host preferences of Sycophila parasitoid wasps associated with oak galls using phylogenomic data
<p>Cryptic species diversity is a major challenge for the species-rich community of parasitoids attacking oak gall wasps due to a high degree of sexual dimorphism, morphological plasticity, small size, and poorly known biology. As such, we know very little about the number of species present, nor the evolutionary forces responsible for generating this diversity. One hypothesis is that trait diversity in the gall wasps, including the morphology of the galls they induce, has evolved in response to selection imposed by the parasitoid community, with reciprocal selection driving diversification of the parasitoids. Using a rare, continental-scale data set of <em>Sycophila</em> parasitoid wasps reared from 44 species of cynipid galls from 18 species of oak across the US, we combined mitochondrial DNA barcodes, Ultraconserved Elements (UCEs), morphological, and natural history data to delimit putative species. Using these results, we generate the first large-scale assessment of ecological specialization and host association in this species-rich group, with implications for evolutionary ecology and biocontrol. We find most <em>Sycophila</em> target specific subsets of available cynipid host galls with similar morphologies, and generally attack larger galls. Our results suggest that parasitoid wasps such as <em>Sycophila</em> have adaptations allowing them to exploit particular host trait combinations, while hosts with contrasting traits are resistant to attack. These findings support the tritrophic niche concept for the structuring of plant-herbivore-parasitoid communities.</p>
Fig. 1 in Distributional range of the South African maritime spider-egg parasitoid wasp, Echthrodesis lamorali (Hymenoptera: Platygastridae: Scelioninae)
Fig. 1. Lateral view of the habitus of a female Echthrodesis lamorali Masner specimen.
Data from: Evolution of flexible biting in hyperdiverse parasitoid wasps
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The emergence of ecotypes in a parasitoid wasp: a case of incipient sympatric speciation in Hymenoptera?
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State of the spread of the exotic parasitoid wasp <em>Leptopilina japonica</em> tracking the route of its invasive host fly <em>Drosophila suzukii</em> in France
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Supplementary information from: Dating the origin of a viral domestication event in parasitoid wasps attacking Diptera
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Data from: Host identity, nest quality, and parasitism strategy: influences on body size variation in parasitoid bees and wasps
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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.