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Figures 815-826. Hind wings. 815 in Morphology of Baridinae and related groups (Coleoptera, Curculionidae)
Figures 815-826. Hind wings. 815, Embates chaetopus, showing 1A and 1A defined near wing margin 1 2 and developed 3A merging with A; 816, Diorymerus lancifer, showing R3 forming a thin, sclerotized vein; 817, Cyrionyx camelus, showing reduced mst; 818, Solaria curtula, indicating absence of rm and showing developed mst; 819, Palmelampius heinrichi, showing reduced 3A; 820, Pycnotheantis sp., showing developed rm; 821, Telemus sp., showing R3 forming a thin, sclerotized vein, developed 3A merging with A, and 1A and 1A defined near wing margin; 822, Megabaris quadriguttata, showing R3 forming a thin, 1 2 sclerotized vein; 823, Zygobaris sp.; 824, Trachymeropsis palmipes, showing reduced 3A; 825, Cyrtepistomus castaneus, showing reduced pst, reduced mst, and developed 3A merging with A; 826, Cryptorhynchus lapathi, showing developed 3A.
Figures 827-840. Hind wings. 827 in Morphology of Baridinae and related groups (Coleoptera, Curculionidae)
Figures 827-840. Hind wings. 827, Dryophthorus americanus; 828, Bagous transversus; 829, Cholus rana; 830, Cossonus impressifrons; 831, Curculio pardalis; 832, Hylurgops planirostris; 833, Testalthea sp.; 834, Pacomes distortus; 835, Trichodocerus sp.; 836, Coeliodes flavicaudis; 837, Mononychus vulpeculus; 838, Hypurus bertrandi; 839, Trigonocolus curvipes; 840, Mecopus trilineatus.
Figures 841-845. Hind wings. 841 in Morphology of Baridinae and related groups (Coleoptera, Curculionidae)
Figures 841-845. Hind wings. 841, Cylindrocopturus adspersus; 842, Telephae oculata; 843, Balanogastris kolae; 844, Metialma signifera; 845, Cyllophorus fausciatus.
Figures 803-814. Hind wings. 803 in Morphology of Baridinae and related groups (Coleoptera, Curculionidae)
Figures 803-814. Hind wings. 803, Centrinus curvirostris; 804, Optatus palmaris, showing 1A and 1A 1 2 defined near wing margin, developed mst, and R3 forming a white line due to loss of sclerotization; 805, Eutoxus sp., showing developed 3A; 806, Parasaldius sp., showing developed rm and 1A and 1A defined 1 2 near wing margin; 807, Buchananius sulcatus; 808, Haplostethops ellipsoidea, showing reduced mst; 809, Linogeraeus viduatus, showing reduced 3A; 810, Plocamus echidna, showing reduced pst; 811, Plocamus clavisetis; 812, Odontocorynus scutellumalbum; 813, Lipancylus brevirostris, showing 1A extending dorsally 2 and merging with A through a -a, developed rm, and developed 3A; 814, Orchidophilus aterrimus, indi1 2 cating absence of rm.
FIGURES 8 – 10. Hind wing. 8 — Proteros sempiternus gen. n in Phylogeny of the tribe Erotini (Coleoptera, Lycidae), with descriptions of new taxa
FIGURES 8 – 10. Hind wing. 8 — Proteros sempiternus gen. n., sp. n.; 9 — Flagrax auberti (Bourgeois); 10 — Aferos sp.
FIGURES 11 – 13. Hind wing. 11 in Phylogeny of the tribe Erotini (Coleoptera, Lycidae), with descriptions of new taxa
FIGURES 11 – 13. Hind wing. 11 — Eros humeralis (Fabricius); 12 — Platycis minuta (Fabricius); 13 — Eropterus arculus Green.
Fig. (18-26): (18) D. laetatorius, hind wing; (19) Netelia sp., hind wing; (20) Netelia sp., frontal view of head; (21) D. laetatorius, propodeum; (22) Syrphophilus bizonarius, propodeum; (23) D. laetatorius, dorsal aspect of metasoma; (24) Netelia sp., lateral aspect of first metasomal segment showing glymma; (25) Exetastes syriacus, ovipositor; (26) Exeristes roborator, ovipositor. in Ichneumonidae from the Suez Canal region Egypt (Hymenoptera, Ichneumonoidea)
Fig. (18-26): (18) D. laetatorius, hind wing; (19) Netelia sp., hind wing; (20) Netelia sp., frontal view of head; (21) D. laetatorius, propodeum; (22) Syrphophilus bizonarius, propodeum; (23) D. laetatorius, dorsal aspect of metasoma; (24) Netelia sp., lateral aspect of first metasomal segment showing glymma; (25) Exetastes syriacus, ovipositor; (26) Exeristes roborator, ovipositor.
Figs 32–34. Nogodinidae, hind wing. 32 in Notes on higher classification of the family Nogodinidae (Hemiptera: Auchenorrhyncha: Fulgoroidea), with description of new tribe and new species
Figs 32–34. Nogodinidae, hind wing. 32 – Forculus gibbosus Distant, male, holotype, Ceylon (BMNH); 33 – Nogodina reticulate (F.), male, Santorem (ZIN); 34 – Bladina sp., Columbia (ZIN).
Figs. 7 and 8. Wing venation. Fig. 7 in A new tribe of Tropiduchidae (Hemiptera: Fulgoroidea) with revision of the genus Buca and description of asymmetric hind leg spinulation
Figs. 7 and 8. Wing venation. Fig. 7. Wing venation of Buca simplex Walker; A) forewing (holotype); B) hind wing (Bolivia). Annotations: A1, A2 = anal veins; B = basal cell; C1, C2, C3 (C3a, C3', C3b), C4 = Cells 1-4; C = Costa; CA = anterior Costa; CP = posterior Costa; CuA = anterior Cubitus; CuP = posterior Cubitus; cup- (pcu+a1) = transverse vein from CuP to Cpu+A1 veins; im = intramedial crossvein; m-cu = medial-cubitus crossvein; MP = posterior Media; Pc = Precosta; PcA = anterior Precosta; Pcu = postcubitus; r-m = radial-media crossvein; R = Radius; RP = posterior Radius; ScP = posterior Subcosta. Fig. 8. Forewing venation; A) Buca asymmetrospinata sp. nov. (paratype); B) Buca truncoptera sp. nov. (holotype). Annotations: A1, A2 = anal veins; B = basal cell; C1, C2, C3 (C3a, C3', C3b), C4, C5 = Cells 1-5; C = Costa; CA = anterior Costa; CP = posterior Costa; CuA = anterior Cubitus; CuP = posterior Cubitus; cup-(pcu+a1) = transverse vein from CuP to Cpu+A1 veins; im = intramedial crossvein; m-cu = medial-cubitus crossvein; MP = posterior Media; Pc = Precosta; PcA = anterior Precosta; Pcu = postcubitus; r-m = radialmedia crossvein; R = Radius; RP = posterior Radius; ScP = posterior Subcosta.
Fig. 2 in Phylogenomics and deep convergence in cockroach hind-wing morphology
Fig. 2 Oulopteryx illuminata sp. nov. is demonstrative of a typical species with an apical folded membrane, but having a rare method of concealment at rest (i.e., coiling, a feature shared among Oulopterygidae, Theganopteryx, Prosoplecta, and possibly a few others). Forewing (a, b) and hind-wing (c) morphology to scale with full body (f, g). Folding occurs alone dashed lines. Method of rolling the hind-wing apical field at rest shown (h). Genital morphology (d, e) of male holotype from posterior dorsal views (d) and dorsal view (e). Labels identify genital sclerites using the nomenclature of Klass (1997). See supplementary figures for more details. Wing venation (b, c) nomenclature based on Li et al. (2018) with modification. *Pcu not identified. See Schubnel et al. (2019) for a discussion of Pcu's identity among Blattodea.
Figure 18-20. Hind wings. 18 in A new genus of telephanine Silvanidae (Coleoptera: Cucujoidea), with a diagnosis of the tribe and key to genera
Figure 18-20. Hind wings. 18) Australophanus redtenbacheri. 19) Euplatamus sp., Bolivia. 20) Aplatamus sp., Mexico.
FIGuru; 5.-Pyrrltoneura bivittata: a, tegmen; b, hind wing; c, lateral view of male genitalia; d, ventral view of male genitalia; e, dorsal view of head and thorax; f, frontal view. in Homoptera, Fulgoroidea and Jassoidea of Guam
FIGuru; 5.-Pyrrltoneura bivittata: a, tegmen; b, hind wing; c, lateral view of male genitalia; d, ventral view of male genitalia; e, dorsal view of head and thorax; f, frontal view.
FIGURES 22–30. Right hind wing. 22 in Revision of Melanocryptus Cameron (Ichneumonidae, Cryptinae), with description of seven new species
FIGURES 22–30. Right hind wing. 22, Melanocryptus niger, female from Bolivia. 23, M. niger, female from Colombia. 24, M. tupan, female from southern Brazil. 25, M. tupan, male from southeastern Brazil. 26, M. aurantius, female holotype. 27, M. whartoni, male from French Guiana. 28, M. tesselatus, female holotype. 29, M. delos, female. 30, M. hadroglyptus, female holotype.
Figure 7. Grumichella blahniki, male. A, forewings. B, hind wings. C in Phylogeny and revision of the Neotropical genus Grumichella Müller (Trichoptera: Leptoceridae), including nine new species and a key
Figure 7. Grumichella blahniki, male. A, forewings. B, hind wings. C, genitalia, lateral view. D, genitalia, dorsal view. E, phallus, lateral view. F, inferior appendage, ventral view.
Fig. 36. Character 33. Hind wing anal lobe, states 0 and 1 in An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
Fig. 36. Character 33. Hind wing anal lobe, states 0 and 1: (0) broad with vein 3A usually strongly curved at distal end, long and separated from wing margin; (1) narrow with vein 3A tending straight, short and usually adjacent to wing margin.
Fig. 35. Character 32. Hind wing 1 in An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
Fig. 35. Character 32. Hind wing 1st cubital cell width at distal ends, states 0 and 1: (0) about equal to 2nd cubital cell; (1) much greater than 2nd cubital cell (twice or more).
Figures 7–12. - Neohemisphaeriusguangxiensis sp. n. 7 Hind wing 8 Male genitalia, in lateral view 9 Aedeagus, in left view 10 Aedeagus, ventral view 11 Genital style, in profile view 12 Anal tube, in dorsal view.
Figures 7–12. - Neohemisphaeriusguangxiensis sp. n. 7 Hind wing 8 Male genitalia, in lateral view 9 Aedeagus, in left view 10 Aedeagus, ventral view 11 Genital style, in profile view 12 Anal tube, in dorsal view.
Figure 1. Landmarks and curves selection. A. Fore wing. B. Hind wing. C in Geometric morphometric analysis of Eysarcoris guttiger, E. annamita and E. ventralis (Hemiptera: Pentatomidae)
Figure 1. Landmarks and curves selection. A. Fore wing. B. Hind wing. C. Pygophore.
Figure 3. PCA analysis. A. Fore wing. B. Hind wing. C in Geometric morphometric analysis of Eysarcoris guttiger, E. annamita and E. ventralis (Hemiptera: Pentatomidae)
Figure 3. PCA analysis. A. Fore wing. B. Hind wing. C. Pygophore.
Phylogenomics and deep convergence in cockroach hind-wing morphology
<p>Despite regular advances in Blattodea systematics, several relationships remain controversial or untested in formal phylogenetic reconstructions. This common situation for understudied metazoan groups limits our power to answer questions about phenotypic evolution. In this study, we infer the evolutionary history of Blattodea using newly sampled taxa that improve phylogenetic resolution while also illuminating the evolutionary history of an unusual phenotype—the apically folded hind-wing. Taxa newly sequenced include those with a hind-wing apical fold (<em>Anaplecta pulchella, A. pygmaea, A. </em>sp<em>. </em>cf<em>. malaysensis, Diplopterina parva, Prosoplecta semperi, Anaplectoidea klossi, </em>and<em> Oulopteryx illuminata</em> sp. nov. that we describe herein, including its male genitalia) and other rare taxa (<em>Dipteretrum</em> <em>hamstroemi</em>, <em>Duchailluia</em> <em>togoensis</em>, <em>Lauraesilpha</em> <em>mearetoi</em>, <em>Buboblatta</em> <em>vlasaki</em>). The phylogenetic design utilizes 41 genes over 91 species in total, analyzed in a maximum likelihood and coalescent framework. To quantify the phylogenetic uncertainty of the analysis, support for various topologies is assessed. We find unambiguous support for the surprising position of Neotropical <em>Oulopteryx</em> (Oulopterygidae) as sister to New Caledonian/Australian Tryonicidae. This, and other phylogenetic findings, reveal that the apically folded hind-wing may have arisen nine times in Blattodea. Further investigations are needed, notably with an increased taxonomic sampling, to demonstrate stronger support for the placement of rogue taxa (e.g., <em>Anaplecta</em>) and to investigate the evolutionary correlates of wing evolution.</p>
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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