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Figure 14 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 14. Cladogram resulting from secondary analysis: section 1 (of 9), outgroups and tribes of Pimplini, showing characters supporting both the monophyly of the subfamily and the several tribes. Note that the topology of this cladogram is essentially the same as that in Fig. 1 except for the re-arrangement of the three tribes of Pimplinae: the Delomeristini is the sister-lineage to Pimplini + Ephialtini, rather than the Pimplini being the sister-group to the Delomeristini + Ephialtini.
Figure 18 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 18. Cladogram resulting from secondary analysis: section 5 (of 9), the basal Ephialtini. Note that the topology is very similar to the primary analysis (Fig. 6) except that the Ephialtes, Camptotypus and Sericopimpla genus-groups form an unresolved trichotomy.
Figure 10 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 10. Cladogram resulting from primary analysis: section 10 (of 13), the basal members of the Sericopimpla genusgroup. Note the demonstrably monophyletic nature of most genera (Sericopimpla, Tromatobia, Zaglyptus and Clistopyga) and their basal relationship to the Polysphincta genus-complex (the Polysphinctini of authors). Gregopimpla is apparently paraphyletic with respect to Iseropus.
Figure 11 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 11. Cladogram resulting from primary analysis: section 11 (of 13), the basal members of the Polysphincta genuscomplex. Note the most basal position of Piogaster and the division of the remaining genera into two monophyletic clades, one comprising Dreisbachia, Schizopyga and Zabrachypus, the other Polysphincta plus the remaining genera. In the first clade Zabrachypus and Schizopyga are monophyletic but Dreisbachia is paraphyletic with respect to them. In the second clade, Oxyrrhexis is paraphyletic.
Figure 12 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 12. Cladogram resulting from primary analysis: section 12 (of 13), the more derived members of the Polysphincta genus-complex. Note that Eriostethus + Zatypota form a well-defined monophyletic group with each genus monophyletic, and Hymenoepimecis + Acrotaphus is also a well-defined clade with each genus monophyletic. However, Polysphincta is polyphyletic (see also Figs 11, 13).
Figure 9 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 9. Cladogram resulting from primary analysis: section 9 (of 13), the more derived members of the Ephialtes genusgroup. Whilst most genera (Townesia, Ephialtes, Liotryphon, Pimplaetus, Leptopimpla Calliephialtes, Umanella, Xanthephialtes and Anastelgis) are monophyletic, Dolichomitus is polyphyletic.
Figures 83–86 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 83–86. Head, lateral; 83, Delomerista mandibularis; 84, Apechthis compunctor; 85, Acrotaphus tibialis; 86, Acrodactyla madida.
Figure 21 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 21. Cladogram resulting from secondary analysis: section 8 (of 9), the basal members of the Sericopimpla genusgroup. The topology of this cladogram is the same as that obtained in the primary analysis, and the monophyly of Gregopimpla not established with respect to Iseropus.
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.
Figure 5 in Morphology and biology of the Miocene butterflyfish Chaetodon ficheuri (Teleostei: Chaetodontidae)
Figure 5. Chaetodon (Arambourgchaetodon) ficheuri Arambourg, 1927. A, holotype, MNHN ORA89, urohyal, left lateral view. Scale bar 5 mm. B, holotype, MNHN ORA89, particular of the gill rakers, left lateral view. Scale bar 1 mm. C, holotype, MNHN ORA89, supracleithrum, left medial view. Scale bar 3 mm. D, holotype, MNHN ORA89, reconstruction of the caudal skeleton, left lateral view. Scale bar 5 mm. E, paratype, MNHN ORA46, supraneurals and first dorsal pterygiophore, right lateral view. Scale bar 5 mm. Abbreviations: ep, epural; hyp, hypural; ns, neural spine; phy, parhypural; pt, pterygiophore; sn, supraneural; soc, supraoccipital; un, uroneural.
Figure 4 in Morphology and biology of the Miocene butterflyfish Chaetodon ficheuri (Teleostei: Chaetodontidae)
Figure 4. Chaetodon (Arambourgchaetodon) ficheuri Arambourg, 1927, reconstruction of the head, left lateral view. Abbreviations: aa, angulo-articular; d, dentary; dsp, dermosphenotic; ecp, ectopterygoid; enp, endopterygoid; epo, epioccipital; fr, frontal; h, hyomandibula; io, infraorbital bones; iop, interopercle; l, lacrimal; le, lateral ethmoid; me, mesethmoid; mtp, metapterygoid; mx, maxilla; n, nasal; op, opercle; pa, parietal; pal, palatine; pmx, premaxilla; pop, preopercle; pto, pterotic; pts, pterosphenoid; q, quadrate; soc, supraoccipital; sop, subopercle; sym, symplectic.
Figure 3 in Morphology and biology of the Miocene butterflyfish Chaetodon ficheuri (Teleostei: Chaetodontidae)
Figure 3. Chaetodon (Arambourgchaetodon) ficheuri Arambourg, 1927. A, paratype, MNHN ORA46. B, paratype, MNHN ORA47. C, MNHN ORA1435. D, paratype, MNHN ORA46. Scale bar 20 mm.
ScienceDex guides
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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.