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FIGURE 27 in A taxonomic review of the genus Callilanguria Crotch, 1876 (Coleoptera: Erotylidae: Languriinae)
FIGURE 27. Mouthparts of both sexes of Callilanguria weiweii Huang & Yang, sp. nov. A–D. Mouthparts of a non-type specimen, male; E–H. Mouthparts of a non-type specimen, female; A, E. Mandibles, dorsal view; B, F. Labrum, ventral view; C, G. Mentum and labium, ventral view; D, H. Maxillae, ventral view. Scale bar = 1 mm.
FIGURES 9–12 in A taxonomic review of the genus Callilanguria Crotch, 1876 (Coleoptera: Erotylidae: Languriinae)
FIGURES 9–12. Dorsal habitus: 9) holotype, Callilanguria ruficeps Achard, 1923; 10) holotype, Callilanguria stenosoma (Harold, 1879); 11) holotype, Callilanguria wallacii Crotch, 1876; 12) holotype, Doubledaya scrupulosa (Heller, 1918) comb. nov.
FIGURES 21–26 in A taxonomic review of the genus Callilanguria Crotch, 1876 (Coleoptera: Erotylidae: Languriinae)
FIGURES 21–26. Paratype of Callilanguria weiweii Huang & Yang, sp. nov., female: 21) dorsal habitus; 22) ventral habitus; 23) tergite VIII, dorsal view; 24) tergite IX, ventral view; 25) spermathecal capsule, lateral view; 26) ovipositor, dorsal view.
FIGURES 6–8 in A taxonomic review of the genus Callilanguria Crotch, 1876 (Coleoptera: Erotylidae: Languriinae)
FIGURES 6–8. Dorsal habitus: 6) holotype, Callilanguria helleri Huang & Yang, sp. nov.; 7) holotype, Callilanguria milloti Villiers, 1945; 8) holotype, Callilanguria nigripes Huang & Yang, sp. nov.
FIGURE 18 in The genus Tarsonemus Canestrini and Fanzago, 1876 (Acari: Heterostigmatina: Tarsonemidae) in East Azerbaijan, Iran, with a description of T. lenticulatus sp. nov. and re-description of T. annotatus Livshits, Mitrofanov and Sharonov, 1979
FIGURE 18. Details of morphology, Tarsonemus lenticulatus sp. nov.: A—pharynx, C—tegula; Tarsonemus annotatus Livshits, Mitrofanov and Sharonov, 1979: B—pharynx, D—tegula. Scale bars are 10 µm.
FIGURES 14–17 in The genus Tarsonemus Canestrini and Fanzago, 1876 (Acari: Heterostigmatina: Tarsonemidae) in East Azerbaijan, Iran, with a description of T. lenticulatus sp. nov. and re-description of T. annotatus Livshits, Mitrofanov and Sharonov, 1979
FIGURES 14–17. Tarsonemus annotatus Livshits, Mitrofanov and Sharonov, 1979—female legs: 14—leg I (dorsal aspect), 15—leg II (dorsal aspect), 16—leg III (16a-ventral aspect, 16b—femorogenu III—female specimen), 17—leg IV (ventral aspect).
FIGURES 12–13 in The genus Tarsonemus Canestrini and Fanzago, 1876 (Acari: Heterostigmatina: Tarsonemidae) in East Azerbaijan, Iran, with a description of T. lenticulatus sp. nov. and re-description of T. annotatus Livshits, Mitrofanov and Sharonov, 1979
FIGURES 12–13. Tarsonemus annotatus Livshits, Mitrofanov and Sharonov, 1979—female gnathosoma: 12—dorsum, 13— venter.
FIGURES 5–8 in The genus Tarsonemus Canestrini and Fanzago, 1876 (Acari: Heterostigmatina: Tarsonemidae) in East Azerbaijan, Iran, with a description of T. lenticulatus sp. nov. and re-description of T. annotatus Livshits, Mitrofanov and Sharonov, 1979
FIGURES 5–8. Tarsonemus lenticulatus sp. nov., female legs: 5–leg I (dorsal aspect), 6–leg II (dorsal aspect), 7–leg III (ventral aspect), 8–leg IV (ventral aspect).
FIGURES 23–24. Distribution maps. 23 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 23–24. Distribution maps. 23, Omorgus triestinae Pittino, 1987; 24, Omorgus suberosus (Fabricius, 1775).
FIGURES 19–22 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 19–22. Omorgus suberosus (Fabricius, 1775), male. 18, habitus, dorsal view; 19, aedeagus, ventral view; 20, aedeagus, with parameres intentionally spread out to show the shape of the median lobe; 21, aedeagus, lateral view (Drawings courtesy (fig. 20): R. Pittino).
FIGURES 14–18. Omorgus triestinae Pittino, 1987, male. 14 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 14–18. Omorgus triestinae Pittino, 1987, male. 14, habitus, dorsal view (red arrows indicate discontinuous yellow tomentosity and white arrows indicate median-basal and lateral-basal tubercles of pronotum); 15, aedeagus, dorsal view; 16, aedeagus, with parameres intentionally spread out to show the shape of the median lobe; 17, aedeagus, lateral view; 18, sclerotized piece of the endophallus (Drawings courtesy (figs. 15 and 18): R. Pittino).
FIGURES 10–12 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 10–12. Form of pronotum and scutellum. 10, Polynoncus juglans (after Ratcliffe 1978, modified); 11, Polynoncus vazdemelloi new species (Abp = antero-basal projection); 12, Polynoncus gemmingeri.
FIGURES 7–9 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 7–9. Polynoncus gemmingeri (Harold, 1872), ♂. 7, habitus, dorsal view; 8, aedeagus, dorsal view; 9, aedeagus, lateral view.
FIGURES 4–6 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 4–6. Polynoncus juglans (Ratcliffe, 1978), ♂. 4, habitus, dorsal view; 5, aedeagus, dorsal view; 6, aedeagus, lateral view.
FIGURES 1–3 in A new species of Polynoncus Burmeister, 1876 from Brazil (Coleoptera: Trogidae)
FIGURES 1–3. Polynoncus vazdemelloi new species, Paratype ♂. 1, Habitus, dorsal view; 2, aedeagus, dorsal view; 3, aedeagus, lateral view.
FIGURES 62a–e. Nomioides turanica Morawitz, 1876 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution II. Family Halictidae, subfamilies Rophitinae, Nomiinae, and Nomioidinae
FIGURES 62a–e. Nomioides turanica Morawitz, 1876. Lectotype, male: a—habitus, lateral view; b—T1–T3, dorsal view; c—head, frontal view; d—mesosoma, dorsal view; e—labels.
FIGURES 51a–e. Nomioides parviceps Morawitz, 1876 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution II. Family Halictidae, subfamilies Rophitinae, Nomiinae, and Nomioidinae
FIGURES 51a–e. Nomioides parviceps Morawitz, 1876. Holotype, male: a—habitus, lateral view; b—metasoma, dorsal view; c—head, frontal view; d—mesosoma, dorsal view; e—labels.
FIGURES 19a–g. Rhophites caucasicus Morawitz, 1876 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution II. Family Halictidae, subfamilies Rophitinae, Nomiinae, and Nomioidinae
FIGURES 19a–g. Rhophites caucasicus Morawitz, 1876. Lectotype, male: a—habitus, dorsal view; b—metasoma, dorsal view; c—F9–F11, lateral view; d—head, frontal view; e—mesosoma, dorsal view; f—S6, ventro-lateral view; g—labels.
Figs. 14–15 in Aleochara verecunda Sharp, 1876 Rediscovered from the Brazilian Amazon (Coleoptera: Staphylinidae: Aleocharinae)
Figs. 14–15. Forest fragment where Aleochara (A.) verecunda has been collected (Brazil, Acre). 14) Aerial photograph; 15) Detail of the area.
Data from: Phylogenetic revision of Minyomerus Horn, 1876 sec. Jansen & Franz, 2015 (Coleoptera, Curculionidae) using taxonomic concept annotations and alignments
This contribution adopts the taxonomic concept annotation and alignment approach. Accordingly, and where indicated, previous and newly inferred meanings of taxonomic names are individuated according to one specific source. Articulations among these concepts and pairwise, logically consistent alignments of original and revisionary classifications are also provided, in addition to conventional nomenclatural provenance information. A phylogenetic revision of the broad-nosed weevil genera Minyomerus Horn, 1876 sec. O'Brien & Wibmer (1982), and Piscatopus Sleeper, 1960 sec. O'Brien & Wibmer (1982) (Curculionidae [non-focal]: Entiminae [non-focal]: Tanymecini [non-focal]) is presented. Prior to this study, Minyomerus sec. O'Brien & Wibmer (1982) contained seven species, whereas the monotypic Piscatopus sec. O'Brien & Wibmer (1982) was comprised solely of P. griseus Sleeper, 1960 sec. O'Brien & Wibmer (1982). We thoroughly redescribe these recognized species-level entities and furthermore describe ten species as new to science: M. bulbifrons sec. Jansen & Franz (2015) (henceforth: [JF2015]), sp. n., M. aeriballux [JF2015], sp. n., M. cracens [JF2015], sp. n., M. gravivultus [JF2015], sp. n., M. imberbus [JF2015], sp. n., M. reburrus [JF2015], sp. n., M. politus [JF2015], sp. n., M. puticulatus [JF2015], sp. n., M. rutellirostris [JF2015], sp. n., and M. trisetosus [JF2015], sp. n. A cladistic analysis using 46 morphological characters of 22 terminal taxa (5/17 outgroup/ingroup) yielded a single most-parsimonious cladogram (L = 82, CI = 65, RI = 82). The analysis strongly supports the monophyly of Minyomerus [JF2015] with eight unreversed synapomorphies, and places P. griseus sec. O'Brien & Wibmer (1982) within the genus as sister to M. rutellirostris [JF2015]. Accordingly, Piscatopus sec. Sleeper (1960), syn. n. is changed to junior synonymy of Minyomerus [JF2015], and its sole member P. griseus sec. Sleeper (1960) is moved to Minyomerus [JF2015] as M. griseus [JF2015], comb. n. In addition, the formerly designated type M. innocuus Horn, 1876 sec. Pierce (1913), syn. n. is changed to junior synonymy of M. microps (Say, 1831) [JF2015] which has priority. The genus is widespread throughout western North America, ranging from Canada to Mexico and Baja California. Apparent patterns of interspecific diversity of exterior and genitalic morphology, varying host plant ranges, overlapping and widely extending species distributions, suggest an early origin for Minyomerus [JF2015], with a diversification that likely followed the development of North American desert biomes. Three species in the genus – i.e., M. languidus Horn, 1876 [JF2015], M. microps [JF2015], and M. trisetosus [JF2015] – are putatively considered parthenogenetic.
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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
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.