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1,063 results for “fig wasp”
Supplementary material 1 from: Wong D-M, Bain A, Shiao S-F, Chou L-S (2019) Fighting injuries, fig exit, and dimorphism in two species of sycoryctine fig wasp (Chalcidoidea, Pteromalidae). Journal of Hymenoptera Research 74: 105-121. https://doi.org/10.3897/jhr.74.36461
: Data type: species data
Fig. 1 in Dolichogenidea maetoi sp. nov. (Hymenoptera: Braconidae) from Japan, the first parasitoid wasp recorded from Hyblaea fortissima (Lepidoptera)
Fig. 1. Caterpillar of Hyblaea fortissima Butler, 1881, host of Dolichogenidea maetoi Fernandez-Triana & Shimizu sp. nov. A – leaf shelter; B – host caterpillar in the shelter.
Fig. 2 in Dolichogenidea maetoi sp. nov. (Hymenoptera: Braconidae) from Japan, the first parasitoid wasp recorded from Hyblaea fortissima (Lepidoptera)
Fig. 2. Female paratype of Dolichogenidea maetoi Fernandez-Triana & Shimizu sp. nov.A – habitus, lateral; B – head, frontal; C – wings; D – metasoma, dorsal; E – mesosoma, dorsal; F – antenna.
Fig. 4. Cox1 polymorphic sites within a 561 in Phylogenetic notes on the rare Mediterranean digger wasp Psenulus fulvicornis (Schenck, 1857) (Hymenoptera: Crabronidae) new to Switzerland
Fig. 4. Cox1 polymorphic sites within a 561 bp alignment of the P. fulvicornis-Group. Vertical numbers indicate the position of the segregation site in the alignment. Of 561 sites 539 were invariable, 10 singleton variable, and 12 parsimony informative sites. At position 543 of the alignment were three mutations, and replacements at the positions 178 and 472 were nonsynonymous (asterisks). Specimens are arranged according to their genetic distance. The Caucasian specimen PSC-11 was divergent from P. fulvicornis and P. schencki but it was similarly distant to both. Specimens are labelled with the specimen ID, the GenBank accession number or the Barcode Identification Number of the BOLD System (see supplementary Table S1). Rectangles include specimens belonging to the clades I–VI in the phylogenetic analysis (Fig. 5).
Fig. 3 in Phylogenetic notes on the rare Mediterranean digger wasp Psenulus fulvicornis (Schenck, 1857) (Hymenoptera: Crabronidae) new to Switzerland
Fig. 3. Main discriminant characters between females of Psenulus fulvicornis (Schenck, 1857) and P. schencki (Tournier, 1889). (A) Propodeal surface and (B) pygidial area of P. fulvicornis from the City of Zurich, Switzerland (D. Frey & A. Zanetta leg.; M. Řiha det.; R. Neumeyer conf.; WSL coll; GenBank accession Nr. KY039438). (C) Propodeal surface and (D) pygidial area of P. schencki from the City of Zurich (25.05.2015; D. Frey & A. Zanetta leg.; M. Řiha det.; R. Neumeyer conf.; WSL coll; GenBank accession Nr. KY039439). In P. fulvicornis, the lateral surface of the propodeum (A) has short crosswise carinas which gives the texture coarse appearance. This character is unique among females of Central European Psenulus. In P. schencki such crosswise carinas are lacking (C), and the texture is finer. The pygidal area is longer and broader in P. fulvicornis (B) than in P. schencki (D), but this character can be difficult to observe in certain specimens.
Fig. 2 in Phylogenetic notes on the rare Mediterranean digger wasp Psenulus fulvicornis (Schenck, 1857) (Hymenoptera: Crabronidae) new to Switzerland
Fig. 2. (A) Female Psenulus fulvicornis (Schenck, 1857) from the City of Zurich, Switzerland (D. Frey & A. Zanetta leg.; M. Řiha det.; R. Neumeyer conf.; WSL coll; GenBank accession Nr. KY039438). (B) Female Psenulus schencki (Tournier, 1889) from the City of Zurich (25.05.2015; D. Frey & A. Zanetta leg.; M. Řiha det.; R. Neumeyer conf.; WSL coll; GenBank accession Nr. KY039439). Note the (barely visible) oblong spot at the lower end of the mid-tibia, which is a unique and shared character for both taxa among Central European Psenulus species (Jacobs, 2007).
Figs 8-14 in New records of Spider Wasps (Hymenoptera, Pompilidae) from northern Iran with description of a new species
Figs 8-14: (8) Arachnospila satyrus ♂, subgenital plate, ventral view; (9) lateral view; (10) Cryptocheilus schakuhensis ♀ holotype, face; (11) clypeus; (12) antenna; (13) abdomen; (14) propdeum.
Figs 1-7 in New records of Spider Wasps (Hymenoptera, Pompilidae) from northern Iran with description of a new species
Figs 1-7:(1) Arachnospila satyrus ♀, face; (2) antenna; (3) foreleg; (4) propodeum; (5) wing; (6) face; (7) Arachnospila satyrus ♂, genital dorsal view.
Figs 1-3 in Two new species of Spider Wasps (Hymenoptera, Pompilidae), Ctenagenia pagliano from Lebanon and Evagetes liane from Canary Islands
Figs 1-3: (1) Ctenagenia pagliano holotype ♀ dorsal view; (2) Ctenagenia pagliano holotype ♀ face; (3) Ctenagenia pagliano holotype ♀ forewing.
Figs 4-10 in Two new species of Spider Wasps (Hymenoptera, Pompilidae), Ctenagenia pagliano from Lebanon and Evagetes liane from Canary Islands
Figs 4-10: (4) Evagetes liane holotype ♀, lateral view; (5) Evagetes liane holotype ♀, head and mesosoma dorsal view; (6) Evagetes liane holotype ♀, face; (7) Evagetes liane holotype ♀, forebasitarus; (8) Evagetes liane holotype ♀, forewing; (9) Evagetes liane paratype, ♂, lateral view; (10) Evagetes liane paratype, ♂, SGP, ventral view.
Fig. 16 in Ichneumonid wasps from Madagascar. VI. The genus Pristomerus (Hymenoptera: Ichneumonidae: Cremastinae)
Fig. 16. Pristomerus veloma sp. nov. A. ♀, habitus, profile. B. ♀, head, facial. C. ♀, hind femur, profile.
Fig. 12 in Ichneumonid wasps from Madagascar. VI. The genus Pristomerus (Hymenoptera: Ichneumonidae: Cremastinae)
Fig. 12. Pristomerus patator sp. nov. A. ♀, habitus, profile. B. ♀, habitus, dorsal. C. ♀, head, facial. D. ♀, propodeum, dorsal. E. ♀, hind femur, profile. F. ♂, hind femur, profile.
Fig. 7 in Ichneumonid wasps from Madagascar. VI. The genus Pristomerus (Hymenoptera: Ichneumonidae: Cremastinae)
Fig. 7. Pristomerus hansoni sp. nov. A. ♀, habitus, profile. B. ♀, habitus, dorsal. C. ♀, head, facial. D. ♀, hind femur, profile. E. ♂, hind femur, profile.
Fig. 9 in Ichneumonid wasps from Madagascar. VI. The genus Pristomerus (Hymenoptera: Ichneumonidae: Cremastinae)
Fig. 9. Pristomerus keyka sp. nov. A. ♀, habitus, profile. B. ♀, habitus, dorsal. C. ♀, head, facial. D. ♀, hind femur, profile.
Fig. 4 in Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris
Fig. 4. Maximum-clade credibility tree representing the complete Idarnes data set.Tips of the tree are labeled with the host fig taxon name.The four Idarnes species associated with Ficus petiolaris do not form a monophyletic group, suggesting a history of host switching for the Idarnes species associated with F. petiolaris. Additionally, LO2 is not monophyletic but forms two distinct clades, with Idarnes sampled from other host fig trees interspersed between them.The two Idarnes samples collected from Ficus pertusa in sympatry with F. petiolaris cluster with one of the LO2 clades (denoted by a circle). Black squares represent posterior probabilities ≥0.95; gray squares represent posterior probabilities <0.95 and ≥0.5. All other nodes had support values below 0.5. Wasps that formed monophyletic groups and were associated with the same host fig species were collapsed for visual purposes.
Fig. 1. Sampling sites for Idarnes wasps associated with Ficus petiolaris. Idarnes wasps were collected from host F in Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris
Fig. 1. Sampling sites for Idarnes wasps associated with Ficus petiolaris. Idarnes wasps were collected from host F. petiolaris localities distributed across Sonoran Desert habitats in Baja California (1–11) and Sonora (12–16), Mexico. Locales 1–13 are from F. petiolaris subspecies palmeri and locales 14–16 are from F. petiolaris subspecies petiolaris. See Table 1 for additional details.
Fig. 7 in Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris
Fig. 7. Idarnes behavioral assays. (A) The proportion of the total number of Idarnes individuals of each species (N at top) observed ovipositing into syconia of each of four developmental stages, from early female phase to interphase (labeled on right). (B) The proportion of I. flavicollis (LO1) and I. carme (SO1+SO2) wasps developing in inner, middle, and outer ranks of ovules within syconia.
Figs 26–28 in Parasitoid wasps new to Britain (Hymenoptera: Platygastridae, Eurytomidae, Braconidae & Bethylidae)
Figs 26–28. Laelius pedatus (Say, 1836), 26–27. ♀, specimen number BMNH(E)968242. 26. Dorsal habitus. 27. Fore wing. 28. ♂, specimen number BMNH(E)968243, dorsal habitus. Scale bars all 1 mm. © Natural History Museum, London.
Figs 15–19 in Parasitoid wasps new to Britain (Hymenoptera: Platygastridae, Eurytomidae, Braconidae & Bethylidae)
Figs 15–19. Schizoprymnus collaris (Thomson, 1874), ♀ BMNH(E)968229. 15. Lateral habitus. 16. Head. 17. Lateral body. 18. Dorsal head. 19. Mesosoma, posterior tergite 3. Scale bars all 1 mm. © Natural History Museum, London.
Fig. 32 in Synopsis of the parasitoid wasp genus Cotesia Cameron, 1891 (Hymenoptera: Braconidae: Microgastrinae) in Australia, with the description of seven new species
Fig. 32. Cotesia wonboynensis sp. nov., ♀, holotype (ANIC 32 130294) A. Mesoscutellum, propodeum, T1–2. B. Head in dorsal view and anteromesoscutum. C. Habitus in lateral view. D. Fore wing. E. Head in anterior view. F. Habitus in dorsal view. G. Cocoons on host caterpillar (image credit: P. Whitington).
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