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4,956 results for “Ichneumonidae”
Figures 59–64 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 59–64. Stereoscan photographs of Pimplinae. Figs 59–63, propodeum, lateral; 59, Zaglyptus simonis; 60, Echthromorpha atrata; 61, Pimpla sumichrasti; 62, Xanthopimpla aurita; 63, Lissopimpla excelsa. Fig. 64, Pimpla azteca, denticles on dorsal rim of propodeal insertion.
Figures 98–101 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 98–101. Posterior end of metasoma of male, showing position and shape of tergites VII−IX and gonosquama, slightly diagrammatic; 98, Rhyssa persuasoria; 99, Dolichomitus irritator; 100, Xanthopimpla aurita; 101, Pimpla sumichrasti. The condition in outgroups, and thus the presumed plesiomorphic condition in pimplines is shown in the first two figures. Tergites VIII and IX are fused in the subsequent two, and the gonosquama show progressive retraction into the posterior end of the metasoma.
Figure 7 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 7. Cladogram resulting from primary analysis: section 7 (of 13), the Camptotypus genus-group. Note that Odontopimpla, Clydonium, Camptotypus and Parvipimpla are demonstrably monophyletic, but Zonopimpla is paraphyletic. The recognition of 'Hemipimpla' as a distinct genus (for C. pulchripennis) would render the residual Camptotypus paraphyletic.
Figure 8 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 8. Cladogram resulting from primary analysis: section 8 (of 13), the basal members of the Ephialtes genus-group. Note that most genera (Acropimpla, Scambus, Exeristes, Xanthophenax Flavopimpla and Paraperithous were retrieved as monophyletic groups. The recognition of Fredegunda renders Endromopoda paraphyletic.
Figure 6 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 6. Cladogram resulting from primary analysis: section 6 (of 13), the basal Ephialtini. Note the basal position of the Pseudopimpla and Alophosternum genus-groups with respect to the three more derived genus-groups.
Figure 2 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 2. Cladogram resulting from primary analysis: section 2 (of 13), Delomeristini. Note that each of the three genera, Atractogaster, Delomerista and Perithous is strongly monophyletic.
Figure 4 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 4. Cladogram resulting from primary analysis: section 4 (of 13), the higher Pimplini. Note the strongly monophyletic nature of the Xanthopimpla and Pimpla genus-groups, and of the two genera, Lissopimpla and Xanthopimpla, comprising the former group.
Figure 1 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 1. Cladogram resulting from primary analysis: section 1 (of 13), outgroups and tribes of Pimplini, showing characters supporting both the monophyly of the subfamily and the several tribes. Autapomorphies are represented by black rectangles, postulated parallelisms by stippled rectangles, and reversals by white rectangles. This convention is adopted in all subsequent cladograms.
Figure 3 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 3. Cladogram resulting from primary analysis: section 3 (of 13), the basal Pimplini (the Theronia genus-group). Note that the Theronia group is paraphyletic with respect to the Pimpla and Xanthopimpla genus-groups, and that the more restricted genera, Theronia and Neotheronia, are polyphyletic.
Figures 69–71 in The cladistics and biology of the Callajoppa genus-group (Hymenoptera: Ichneumonidae, Ichneumoninae)
Figures 69–71. (69) Trogus pennator (Fabricius), frontal view of head. (70) Gnamptopelta obsidianator, dorsal view of pronotum and anterior of mesoscutum. (71) Conocalama brullei, dorsal view of postpetiole.
Figures 1 in The cladistics and biology of the Callajoppa genus-group (Hymenoptera: Ichneumonidae, Ichneumoninae)
Figures 1. First of three cladograms for the Callajoppa Group. Subsets of this cladogram are shown in Figs 2–4. For this and following cladograms, black bar = apomorphy, grey bar = parallelism, white bar = reversal. All cladograms were made with the Clados program of Nixon (1998a).
Abb. 1 in Die Coelichneumon-Arten (Hymenoptera, Ichneumonidae, Ichneumoninae) des Biologiezentrums Linz, Austria
Abb. 1: Kopf der von (a) Coelichneumon longiterebra nov.sp., (b) C. rufigaster nov.sp., (c) C. paraviolaceiventris nov.sp., (d) C. fasciator nov.sp., (e) C. pararudis nov.sp., (f) C. shanxiensi nov.sp., (g) C. mesonotator nov.sp., (h) C. pamirensis nov.sp.
Fig. 11 in Additions to the Swedish fauna of Diplazontinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
Fig. 11. Woldstedtius patei (Dasch, 1964), holotype, ♀, Colorado, Grand L., 24 Aug. 1940, H. and M. Townes leg. (USUC). A. Habitus, lateral view. B. Propodeum, laterodorsal view. C. Head and mesosoma, lateral view. D. Labels. Photos: David Wahl (USUC).
Fig. 2 in Additions to the Swedish fauna of Diplazontinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
Fig. 2. Homotropus hellqvisti sp. nov., paratype, ♀ (NHRS-HEVA000011637). A. Habitus, lateral view. B. Posterior segments of metasoma.
Fig. 10 in Additions to the Swedish fauna of Diplazontinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
Fig. 10. Woldstedtius aureotibialis sp. nov., paratype, ♀ (NHRS-HEVA000011632). A. Habitus, lateral view. B. Head, anterior view. C. Propodeum, dorsal view. Photos: Alexander Berg.
Fig. 5. A–B in Additions to the Swedish fauna of Diplazontinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
Fig. 5. A–B. Mesoscutum of female, anterodorsal view. A. Homotropus pallipes (Gravenhorst, 1829). B. Homotropus mugerwai sp. nov., paratype (NHRS-HEVA000011633). C–D. Head, anterior view of female. C. Homotropus hellqvisti sp. nov., paratype (NHRS-HEVA000011637). D. Homotropus collinus (Stelfox, 1941). E–F. Posterior segments of metasoma of female. lateral view. E. Homotropus melanogaster (Holmgren, 1872). F. Homotropus collinus.
Fig. 13 in Additions to the Swedish fauna of Diplazontinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
Fig. 13. Seashore along the Baltic sea at Haparanda Santasaari, type locality for Homotropus klopfsteinae sp. nov. Photo: Nils Ryrholm.
Fig. 8 in Additions to the Swedish fauna of Diplazontinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
Fig. 8. Homotropus riedeli sp. nov., holotype, ♀ (NHRS-HEVA000011630). A. Head, anterior view. B. Propodeum, posterodorsal view. C. Mesosoma, lateral view.
Fig. 18 in A new Darwin wasp genus, Soliga (Hymenoptera: Ichneumonidae: Metopiinae), from India
Fig. 18. Soliga ecarinata gen. et sp. nov., holotype, ♀ (AIMB). a. Head and mesosoma, ventral view. b. Propodeum, dorsal view. c. Fore and mid legs. d. Fore wing. e. Metasoma, lateral view. f. Metasoma, dorsal view.
Fig. 13. a in A new Darwin wasp genus, Soliga (Hymenoptera: Ichneumonidae: Metopiinae), from India
Fig. 13. a. Carria sp., mesosoma, dorsal view. b. Colpotrochia sp., metasomal tergite 1, dorsal view. c. Trieces irwini Ranjith & Priyadarsanan, 2022, mesosoma, dorsal view. d. Trieces orientalis Ranjith & Priyadarsanan, 2022, metasomal tergite 1, dorsal view. Arrow in Fig. 13a points to the presence of notauli on mesoscutum (compared to the absence of notauli on mesoscutum in Fig. 13c). Arrow in Fig. 13b points to first metasomal tergite narrow basally (compared to first metasomal tergite broad basally in Fig. 13d).
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International Brain Laboratory public data
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OpenNeuro
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