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565 results for “higher classification”
Figure 4 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 4 - Strict consensus of 38 most-parsimonious trees (length = 2828, ci = 0.19, ri = 0.61), of 101 sub/genera of Mutillidae and 4 outgroups, both sexes, 230 characters many additive and all equally weighted. Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 9 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 9 - Single most-parsimonious tree (raw length = 1134, ci = 0.19, ri = 0.61), of 101 sub/genera of Mutillidae and 4 outgroups, females only, 97 characters many additive and all with implied weighting (N = 5, k = 81). Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
Figure 12 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 12 - Preferred most-parsimonious tree (see Fig. 5) with potential groups incorporating ideas from both previous classifications indicated.
Figure 7 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 7 - Single most-parsimonious tree (raw length = 3822, ci = 0.14, ri = 0.75), of 101 sub/genera of Mutillidae and 4 outgroups (but each duplicated and recoded so as to reflect maximal character-state differences for polymorphisms, and taxa retained as monophyletic collapsed in the figure, see text), both sexes, 230 characters many additive and all with implied weighting (N = 5, k = 169). Group support (GC) values shown for all groups supported by resampling. Names in bold are of "terminals" shown not to be monophyletic.
Figure 15 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 15 - Subtending states for tree reflecting proposed taxa as monophyletic. Blue indicates states found only when most characters were considered additive, red only when all states were considered non-additive, and black under both conditions. Solid hashmarks indicate unique state changes, and open hashmarks are homoplasies. Letters within boxes indicate breaks in branches to enable effective layout.
Figure 11 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 11 - Preferred most-parsimonious tree (see Fig. 5) showing distribution of characters (upper numbers) and states (lower numbers) optimized as in Appendix 2. Asterisks (*) indicate character states unambiguously placed (position not changing under any optimization). Solid hashmarks indicate unique state changes, and open hashmarks are homoplasies. Letters within boxes indicate breaks in branches to enable effective layout. [continued over 5 pages]
Figure 16 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 16 - Final proposed higher classification of Mutillidae, as related to the rearranged tree (cf. Fig. 1).
Figure 8 from: Brothers DJ, Lelej AS (2017) Phylogeny and higher classification of Mutillidae (Hymenoptera) based on morphological reanalyses. Journal of Hymenoptera Research 60: 1-97. https://doi.org/10.3897/jhr.60.20091
Figure 8 - Single most-parsimonious tree (raw length = 2024, ci = 0.21, ri = 0.63), of 101 sub/genera of Mutillidae and 4 outgroups both sexes, 198 characters (32 of the original 230 deleted, those found to be polymorphic in at least 10% of terminals) many additive and all with implied weighting (N = 5, k = 81). Group support (GC) values shown for all groups supported by resampling. Terminals in bold are those whose placements differ by more than mere taxonomic level in the classifications of DB and LN (see Appendix 1).
FIGURE 1 in Nomenclatural changes in the higher classification of the family Tettigometridae (Hemiptera: Fulgoroidea) with description of a new tribe and new species and a review of the Iranian tettigometrid fauna
FIGURE 1. Classification history of family Tettigometridae.
Linked collectors and determiners for: Nomenclatural changes in the higher classification of the family Tettigometridae (Hemiptera: Fulgoroidea) with description of a new tribe and new species and a review of the Iranian tettigometrid fauna.
Natural history specimen data linked to collectors and determiners held within, "Nomenclatural changes in the higher classification of the family Tettigometridae (Hemiptera: Fulgoroidea) with description of a new tribe and new species and a review of the Iranian tettigometrid fauna". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/ffbf71d1-4603-4569-8507-110bd0923477">https://bionomia.net/dataset/ffbf71d1-4603-4569-8507-110bd0923477</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/ffbf71d1-4603-4569-8507-110bd0923477">https://gbif.org/dataset/ffbf71d1-4603-4569-8507-110bd0923477</a>. Formatted as a Frictionless Data package.
FIGS. 53–56 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 53–56. Comb setae on the edge and ventral surface of foretarsus basal segment. 53, Australembia incompta (Australembiidae): arrow indicating broad and recumbent comb setae; 54, Antipaluria urichi (Clothodidae); 55, Chelicerca barbara (Anisembiidae): arrow indicating slender comb setae; 56, Oligotoma saundersii (Oligotomidae).
FIGS. 24–28 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 24–28. Shapes of auditory organ on right hind femur: 24, Chelicerca barbara (Anisembiidae); 25, C. wheeleri (Anisembiidae); 26, Australembia incompta (Australembiidae); 27, Anisembia piticial (Anisembiidae); 28, Mesembia chamulae (Anisembiidae).
FIGS. 2–5 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 2–5. General view of the auditory organ on femora indicated by black arrows: 2, Clothoda longicauda female (Clothodidae) forefemora dorsal view; 3, Chelicerca wheeleri male (Anisembiidae) forefemora dorsal view; 4, Chelicerca barbara female, middle and hind femora dorsal view; 5, Chelicerca barbara male, middle and hind femora anterolateral view.
Figure 1 in Molecular phylogeny and systematics of the Pieridae (Lepidoptera: Papilionoidea): higher classification and biogeography
Figure 1. Three different phylogenetic hypotheses of the higher classification of the Pieridae. A, Klots (1933). B, Ehrlich (1958). C, Venables (1993).
Figures 49–60 in Phylogeny and higher classification of suborder Psocomorpha (Insecta: Psocodea: 'Psocoptera')
Figures 49–60. (49–50) female epiproct of Elipsocus abdominalis (49) and Haplophallus sp. (50), dorsal view; (51–55) female genitalia of E. abdominalis (51), Psocidus sp. (52) and Stenopsocus sp. (53), lateral view, Lichenomima muscosa (54) and P. sp. (55), ventral view; (56–59) apex of subgenital plate of E. abdominalis (56), Ectopsocus sp. (57), Heterocaecilius fuscus (58) and Mesopsocus unipunctatus (59); (60) spermatheca of Stenopsocus sp. Abbreviations: epr = epiproct; dv = dorsal valve; ev = external valve; pp = paraproct; sg = subgenital plate; vv = ventral valve.
Figures 1–14 in Phylogeny and higher classification of suborder Psocomorpha (Insecta: Psocodea: 'Psocoptera')
Figures 1–14. (1–5) Head of Echmepteryx lunulata (1) and Psococerastis nubila (2), lateral view; E. lunulata (3), P. nubila (4) and Epipsocopsis sp. (5), anterior view; (6–7) mandible of P. nubila (6) and Matsumuraiella radiopicta (7), anterior view; (8–12) maxilla of P. nubila (8) and M. radiopicta (9), lateral view; Paramphientomum sp. (10) and P. nubila (11), showing muscles attached to galea, anterior view; Notiopsocus aldretei (12), showing apex of lacinia; (13–14) labium of P. nubila (13) and Stenopsocus sp. (14), posterior view. Abbreviations: ata = anterior tentorial arm; cly = clypeus; fr = frons; g = galea; l = lacinia; lr = labrum.
FIGURE 1 in Toward a new classification of planthoppers Hemiptera Fulgoromorpha: 2. Higher taxa, their names and their composition
FIGURE 1. Fulgoromorpha classification summary.
Fig. 32. Character 18. Fore wing ulnar cell 3, states 0 and 1 in An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
Fig. 32. Character 18. Fore wing ulnar cell 3, states 0 and 1: (0) angled to radial cell; (1) substantially parallel to radial cell.
Figs. 1–2 in An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
Figs. 1–2. Head, Tamasa tristigma, Cicadinae: (Fig. 1) anterior view; (Fig. 2) dorsal view. Terminology after Kramer (1950) and Hamilton (1981). Terminologies in brackets also in current use. (ac) anteclypeus; (e) compound eye; (eps) epicranial suture; (epsa) anterior arm of epicranial suture; (fcs, ess) frontoclypeal suture, or epistomal suture; (fl) flagellum of antenna; (flm 2) second flagellomere; (fr) frons; (g) gena; (l, mp) lorum, or mandibular plate; (labi) labium; (labr) labrum; (m) mentum; (oc) ocellus, median or lateral; (oct) ocular tubercle; (pc) postclypeus; (ped) pedicel; (r) rostrum; (s) stylets; (sap) supra-antennal plate; (scp) scape; (tg) transverse groove; (v, ep) vertex, or epicranium.
Figs. 7–11 in An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
Figs. 7–11. Legs, lateral view; pretarsal claws ventral view: (Fig. 7) fore leg, Tamasa tristigma, Cicadinae; (Fig. 8) mid leg, same species; (Fig. 9) hind leg, same species; (Fig. 10) pretarsus, same species; (Fig. 11) pretarsus Tettigarcta crinita, Tettigarctidae. Terminology mostly after Imms (1957). (clw) pretarsal claw (part of distal tarsomere); (cox) coxa; (emp) empodium; (fem) femur; (mc), meracanthus; (mst) mesotarsus; (mtt) metatarsus; (pemp) setiform parempodium; (prt) pretarsus; (psp) primary spine of fore femur; (set) sensory seta; (spu) tibial spur; (ssp) secondary spine of fore femur; (tar) tarsus; (tib) tibia; (tco) tibial comb; (tro) trochanter; (ttco) thumb of tibial comb.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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