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239 results for “gen. et sp. n.”
Figure 5 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 5 - Cecidonius pampeanus last larval instar under light microscopy. A general schematic representation, lateral view B, C head, anterior, and lateral, respectively. Scale bars: 0.5 mm (A); 0.2 mm (B, C).
Figure 4 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 4 - Cecidonius pampeanus genitalia morphology under light microscopy. A schematic representation of male genitalia, lateral view (left valve omitted) B dissected male genitalia, ventral, with detached phallus and juxta, on left and right side, respectively C female genitalia, dorsal D schematic representation of female genitalia, latero-dorsal. Roman numbers indicate abdominal segments. Oviscapt cone is represented in light gray in D. Arrows point to the end of left anterior apophysis in C, and to the apodeme of posterior apophysis in D. Asterisks indicate internal dorsal crest of oviscapt cone in C and D. Open and closed arrow heads point, respectively, to posterior apophyses and cloacal apodemes in D. Abbreviations: cb corpus bursae; cl cloaca; co common oviduct; sp spermatheca; rt rectum; vt vestibulum; ut utriculus of spermatheca. Scale bars: 0.25 mm.
Figure 3 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 3 - Cecidonius pampeanus adult morphology under light microscopy. A head, anterior view B lateral cervical sclerites, anterior; C fore- and hindwing venation, dorsal D metathoracic furcasternum, posterior (closed arrow points to left furcal apophysis) E metathoracic furcasternum in detail, lateral (asterisk indicates left furcal apophysis) F fore-, median- and hindlegs, from left to right, respectively. Scale bars: 0.25 (A, D); 0.1 mm (B); 1 mm (C, F); 0.2 mm (E).
Figure 2 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 2 - Pinned-dried C. pampeanus adults, dorsal view: A male (holotype, LMCI 188-4) B female paratype (LMCI 188-6). Scale bars: 2 mm.
Figure 10 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 10 - Hymenoptera fauna associated with C. pampeanus galls. A transversally sectioned, externally developing gall, showing inside a larva of C. pampeanus (asterisk) with attached larva (arrow) of Lyrcus sp. (Pteromalidae) B transversally sectioned, dried gall, with pupa of Lyrcus (arrow), after consumption of C. pampeanus larva C dried and empty attached galls showing orifices of emergence left by adults of Lyrcus D young, erupting, free of inquiline and adjacent inquiline attacked (Allorhogas sp., Braconidae) galls, indicated respectively by open arrow and asterisk E young galls of C. pampeanus (arrows) partially involved with gall tissue induced by inquilines F variation in size among Allorhogas galls early attacked G a full-developed inquiline-attacked gall showing larvae and pupae in cameras inside H senescent Allorhogas gall showing orifices of emergence (arrows) left by adults. Scale bars: 1 mm (A, B, D, F); 5 mm (C); 0.5 mm (E, G, H).
Figure 11 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 11 - Geographic distribution and genetic variation among populations of C. pampeanus within Rio Grande do Sul State, Brazil; A localities of populations studied (see Suppl. material 3 for exact geographic coordinates and elevations) B evolutionary relationships of COI haplotypes across ten populations. The circles represent haplotypes; the diameter is proportional to the frequency in 60 analyzed individuals. Small red circles indicate intermediate vectors. Transversal bars represent mutational steps. Numbers in parentheses correspond to localities in the map (A) C correlation between pairwise geographic distance and estimates of gene flow (φST) (P<0.05).
Figure 1 from: Moreira GRP, Eltz RP, Pase RB, Silva GT, Bordignon SAL, Mey W, Gonçalves GL (2017) Cecidonius pampeanus, gen. et sp. n.: an overlooked and rare, new gall-inducing micromoth associated with Schinus in southern Brazil (Lepidoptera, Cecidosidae). ZooKeys 695: 37-74. https://doi.org/10.3897/zookeys.695.13320
Figure 1 - Molecular phylogeny of Cecidosidae. Bayesian time-calibrated consensus tree based on cytochrome oxidase subunit I (COI), r16S ribosomal (16S) and Wingless (Wg) genes. Prodoxidae (Greya enchrysa and Tegeticula antithetica) was used to root the tree. Colored branches indicate posterior probability support for the equivalent node following the legend. Dark gray bar indicates confidence interval for each node age estimate, presented in millions of years ago (Mya).
Figures 1-3 from: Palacios-Vargas JG (2017) Honduranura centraliamericana gen. n. et sp. n. from Central America (Collembola, Neanuridae, Neanurinae). ZooKeys 723: 1-9. https://doi.org/10.3897/zookeys.723.12258
Figures 1-3 Honduranura centraliamericana sp. n. 1 habitus on slide 2 antennofrontal + clypeal tubercle 3 dorsal chaetotaxy of head and thoracic segments I–II.
Figures 8-12 from: Palacios-Vargas JG (2017) Honduranura centraliamericana gen. n. et sp. n. from Central America (Collembola, Neanuridae, Neanurinae). ZooKeys 723: 1-9. https://doi.org/10.3897/zookeys.723.12258
Figures 8-12 Honduranura centraliamericana sp. n. 8 lateral view of tibiotarsus III chaetotaxy 9 furcular vestige (midventral region of Abd. III) 10 ventral chaetotaxy of Abd. II–VI 11 female genital plate 12 male genital plate.
Figures 4-7 from: Palacios-Vargas JG (2017) Honduranura centraliamericana gen. n. et sp. n. from Central America (Collembola, Neanuridae, Neanurinae). ZooKeys 723: 1-9. https://doi.org/10.3897/zookeys.723.12258
Figures 4-7 Honduranura centraliamericana sp. n. 4 dorsal chaetotaxy of abdominals segments II–VI 5 dorsal antennal segments III and IV 6 chaetotaxy of pre-labrum/labrum 7 chaetotaxy of labium.
Fig. 16 in Viettagona Vietnamensis Gen. Et Sp. N. From Vietnam (Coleoptera, Tenebrionidae: Blaptini)
Fig. 16. Viettagona vietnamensis gen. et sp. n., female genital tubes. v: vagina; sg: spermathecal gland; ss: spermathecal sphincter; sd: spermathecal duct; r1: 1st reservoir and r2, 2nd reservoirs of
Figure 6 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 6 Philippiphonte aspidosoma gen. et sp. n. (♂): A habitus, dorsal B antennule, ventral [segments 1–4 disarticulated; insert showing apical armature of segment 8 in dorsal aspect] C leg 3 endopod, anterior.
Figure 5 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 5 Philippiphonte aspidosoma gen. et sp. n.: A leg 4 ♀, anterior B urosome ♂ (excluding leg 5-bearing somite), ventral C anal somite and right caudal ramus ♂, dorsal D anal somite and right caudal ramus ♂, ventral E leg 5 ♂, ventral.
Figure 2 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 2 Philippiphonte aspidosoma gen. et sp. n. (♀): A habitus, dorsal [inset showing caudal ramus setae IV–V at full length] B antennule, ventral [inset showing apical armature of segment 5 in dorsal aspect; dorsal setae not shown in ventral aspect marked by *] C antenna.
Figure 1 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 1 Localities in Dokdo island, Korea where Philippiphonte aspidosoma gen. et sp. n. was collected: 1 Gajaebawi (type locality) 2 Mulgol 3 Old harbour.
Figure 4 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 4 Philippiphonte aspidosoma gen. et sp. n. (♀): A anal somite and left caudal ramus, dorsal B anal somite and left caudal ramus, ventral C leg 2, anterior D leg 3, anterior.
Figure 3 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 3 Philippiphonte aspidosoma gen. et sp. n. (♀): A urosome and right leg 5, ventral B mandible [inset showing gnathobase from different angle] C maxillule, anterior [inset showing small unipinnate element arising from posterior surface] D maxilla E maxilliped F leg 1, anterior [exp-2 and -3 disarticulated].
Figure 7 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 7 Harpacticoid copepods exhibiting dorsoventrally flattened body shapes (females only, dorsal view; genital double-somite shaded). A Philippiphonte aspidosoma (Laophontidae) B Porcellidium viride (Philippi, 1840) (Porcellidiidae) C Neopeltopsis pectinipes Hicks, 1976 (Peltidiidae) D Hamondia superba Huys, 1990 (Hamondiidae) E Alteutha oblonga (Goodsir, 1845) (Peltidiidae) F Peltidium purpureum Philippi, 1839 (Peltidiidae) G Zaus abbreviatus Sars, 1904 (Harpacticidae) H Paramenophia platysoma (Thompson & Scott, 1903) (Thalestridae) I Xouthous purpurocinctus (Norman & Scott, 1905) (Pseudotachidiidae) J Xouthous parasimulans (Médioni & Soyer, 1968) (Pseudotachidiidae) K Mucropedia kirstenae Bouck, Thistle & Huys, 1999 (Harpacticidae) L Donsiella phycolimnoriae Hicks, 1990 (Pseudotachidiidae) M Alteuthoides kootare Hicks, 1986 (Peltidiidae) N Peltidiphonte rostrata Gheerardyn & Fiers in Gheerardyn, Fiers, Vincx & De Troch, 2006 (Laophontidae) O Peltobradya bryozoophila Médioni & Soyer, 1968 (Ectinosomatidae) P Scutellidium arthuri Poppe, 1884 (Tisbidae).
Figure 11 from: Silva GT, Moreira GRP, Vargas HA, Gonçalves GL, Mainardi MD, Blas GS, Davis D (2018) Overlooked gall-inducing moths revisited, with the description of Andescecidium parrai gen. et sp. n. and Oliera saizi sp. n. from Chile (Lepidoptera, Cecidosidae). ZooKeys 795: 127-157. https://doi.org/10.3897/zookeys.795.27070
Figure 11 Morphology of Olierasaizi last larval instar under scanning electron microscopy. A head, antero-lateral view B labrum and clypeus, anterior C antenna, lateral D maxilla, anterior E labium, ventral F detail of maxilla (indicated by asterisk) and mandibula (pointed by arrow) bases, showing protuberances G mesothoracic leg rudiment, lateral H callus of third abdominal tergum, latero-dorsal I last abdominal segments, lateral. Scale bars: 250 µm (A), 40 µm (B), 20 µm (C, E, F), 30 µm (D), 60 µm (G), 100 µm (H), 200 µm (I).
Figure 14 from: Silva GT, Moreira GRP, Vargas HA, Gonçalves GL, Mainardi MD, Blas GS, Davis D (2018) Overlooked gall-inducing moths revisited, with the description of Andescecidium parrai gen. et sp. n. and Oliera saizi sp. n. from Chile (Lepidoptera, Cecidosidae). ZooKeys 795: 127-157. https://doi.org/10.3897/zookeys.795.27070
Figure 14 Natural history of Olierasaizi on Schinuspolygamus. A host-plant habitat at Cuesta Barriga, near Santiago city, Chile, 33°31'24"S, 70°54'35"W (asterisk locates the plant; open arrow indicates commune of Padre Hurtado in the valley, Metropolitan region) B apical branches showing swollen stem with galls under bark C pupal exuvium protruded from the gall exit hole, just after the adult emergence (enlarged area pointed by arrow in (B) D intact empty gall, shown by detaching the bark (indicated by arrow) E empty galls, with decaying gall-wall still remaining, lateral F old gall signs appearing as small craters on surface of dried branch. Scale bars: 5 mm (B), 2 mm (C), 3 mm (D, E), 15 mm (F).
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