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378 results for “Green lacewing”
Fig. 6 in The first green lacewings from the late Eocene Baltic amber
Fig. 6. Green lacewing Nothochrysa? sp. from the late Eocene Baltic amber. Wing venation of the SMF-Be-2464, left (A, converted to right dorsal view) and right (B) forewing. Abbreviations: Psc, pseudocubitus; Psm, pseudomedia; RA, anterior radius; RP, posterior radius; ScP, posterior subcosta.
Fig. 5 in The first green lacewings from the late Eocene Baltic amber
Fig. 5. Green lacewing Nothochrysa? sp. from the late Eocene Baltic amber. SMF-Be-2464, general view (A), left forewing (B), costal space of right forewing (C), fragment of right forewing (D).
Fig. 3 in The first green lacewings from the late Eocene Baltic amber
Fig. 3. Green lacewing Pseudosencera baltica gen. et sp. nov. from the late Eocene Baltic amber. Head and legs of the holotype SMF-Be-2518. A. Photograph, fronto-lateral view. B. Line drawing of the head, latero-frontal view. Abbreviations: ant, antenna; ept, epistomal suture; fs, frontal suture; ga, galea; lbr, labrum; lp, labial palpus; mp, maxillary palpus; mtfe, metafemur; mtti, metatibia; pe, pedicellus; pfe, profemur; pti, protibia; sc, scapus; vt, vertex.
Fig. 4 in The first green lacewings from the late Eocene Baltic amber
Fig. 4. Green lacewing Pseudosencera baltica gen. et sp. nov. from the late Eocene Baltic amber. Wing venation of the holotype SMF-Be-2518, right (A) and left (B) forewing, left hind wing (C). B, C converted to right dorsal view. Abbreviations: 1aa1-aa2, first crossvein between AA1 and AA2; 1aa2-aa3, first crossvein between AA2 and AA3; 1icu, first (basal) crossvein between CuA and CuP; 2icu, second crossvein between CuA and CuP; 1cu-aa, fist crossvein between CuP and AA1; 1im, first crossvein between MA and MP; 1m-cu, first (basal) crossvein between M and Cu; AA1–3, first to third anterior analis; CuA, anterior cubitus; CuA1, first (proximal-most) branch of CuA; CuP, posterior cubitus; M, media; MA and MP, anterior and posterior branches of the media; Psc, pseudocubitus; Psm, pseudomedia; RA, anterior radius; RP, posterior radius; RP1–5, first (proximal-most) to fifth branches of RP; ScP, posterior subcosta.
Fig. 2 in The first green lacewings from the late Eocene Baltic amber
Fig. 2. Green lacewing Pseudosencera baltica gen. et sp. nov. from the late Eocene Baltic amber. Holotype (SMF-Be-2518) in dorsal (A) and lateral (B) views.
Fig. 1 in The first green lacewings from the late Eocene Baltic amber
Fig. 1. The intramedian cell, pseudomedia and pseudocubitus in the forewing of green lacewing Pseudosencera baltica gen. et sp. nov. from the late Eocene Baltic amber. Psm and Psc are outlined black in this figure. Abbreviations: 1im, first crossvein between MA and MP; 1m-cu, first (basal) crossvein between M and Cu; CuA, anterior cubitus; CuP, posterior cubitus; M, media; MA and MP, anterior and posterior branches of the media; Psc, pseudocubitus; Psm, pseudomedia; RP, posterior radius; RP1, proximal-most branch of RP; ScP, posterior subcosta.
Figs 1–4 in First record of the green lacewing Chrysoperla nigrocapitata (Neuroptera: Chrysopidae) from Russia
Figs 1–4. Chrysoperla nigrocapitata from Kaimanovka, Primorskii Krai: 1 – netting
FIGURE 12 in Review of the green lacewing genus Apochrysa Schneider (Neuroptera: Chrysopidae)
FIGURE 12. Aberrant wing venation in Apochrysa lutea (Walker) (after Winterton, 2006: fig. 1 A–B) (vestiture and markings omitted).
FIGURE 7 in Review of the green lacewing genus Apochrysa Schneider (Neuroptera: Chrysopidae)
FIGURE 7. Apochrysa spp.: A. Apochrysa leptalea (Rambur); B. Apochrysa voeltzkowi (Weele) (photos: Laura Breitkreuz).
FIGURE 9 in Review of the green lacewing genus Apochrysa Schneider (Neuroptera: Chrysopidae)
FIGURE 9. Wings of Apochrysa spp.: A. Apochrysa cognata (Kimmins) (after Kimmins, 1953: fig 4); B. Apochrysa evanida Gerstaecker (drawn here from type image); C. Apochrysa leptalea (Rambur) (after Kimmins, 1952: fig. 7); D. Apochrysa lutea (Walker) (after Kimmins, 1952: fig. 2) (Note: figures not to scale and vestiture omitted).
FIGURE 7 in The green lacewing genus Austrochrysa Esben-Petersen, 1928 (Neuroptera: Chrysopidae) from China, with description of two new species
FIGURE 7. Known distribution of Austrochrysa Esben-Petersen, 1928 species from China. Austrochrysa tropica (Yang & Wang) (black triangle); Austrochrysa lihongyui sp. nov. (black circle); Austrochrysa angusta sp. nov. (black square).
FIGURE 6 in The green lacewing genus Austrochrysa Esben-Petersen, 1928 (Neuroptera: Chrysopidae) from China, with description of two new species
FIGURE 6. Austrochrysa angusta sp. nov. (Yunnan, Menglun, holotype, male), male abdomen. A. Terminal segments, lateral view; B. Terminal segments, ventral view; C. Mediuncus, lateral view; D. Mediuncus, ventral view; E. Gonarcus and entoprocessus, lateral view; F. Tignum, dorsal view. Austrochrysa angusta sp. nov. (Yunnan, Menglun, paratype, female), female abdomen. G. spermatheca; H. Segment A7-terminus, lateral view; I. Segment A7-terminus, ventral view. cc callus cerci; ent entoprocessus; gcr gonocristae; g.l. gonaphophyses lateralis; gon gonarcus; S7 sternum 7; S8 sternum 8; sg subgenitale; sm spermatheca; T7 tergum 7; T8 tergum 8; T9+e tergum 9+ectoprocts.
FIGURE 3 in The green lacewing genus Austrochrysa Esben-Petersen, 1928 (Neuroptera: Chrysopidae) from China, with description of two new species
FIGURE 3. Austrochrysa lihongyui sp. nov. (Xizang, Mêdog, Miri vill., holotype, male). A. Head, frontal view; B. Thorax, dorsal view; C. Forewing; D. Hind wing; E. Line drawing of hind pretarsal claw.
FIGURE 5 in The green lacewing genus Austrochrysa Esben-Petersen, 1928 (Neuroptera: Chrysopidae) from China, with description of two new species
FIGURE 5. Austrochrysa angusta sp. nov. (Yunnan, Menglun, paratype, male). A. Head, frontal view; B. Thorax, dorsal view; C. Forewing and hind wing; D. Line drawing of hind pretarsal claw.
FIGURE 2 in The green lacewing genus Austrochrysa Esben-Petersen, 1928 (Neuroptera: Chrysopidae) from China, with description of two new species
FIGURE 2. Yunchrysopa tropica Yang & Wang (Yunnan, Jinghong, holotype, male), male abdomen. A. Segment A7-terminus, lateral view; B. Segment A7-terminus, ventral view; C. Gonarcal complex, lateral view; D. Tignum, dorsal view; E. Mediuncus, ventral view. cc callus cerci; ent entoprocessus; gcr gonocristae; gsac gonosaccus; gon gonarcus; mu mediuncus; S8 sternum 8; T8 tergum 8; T9+e tergum 9+ectoprocts.
FIGURE 4 in The green lacewing genus Austrochrysa Esben-Petersen, 1928 (Neuroptera: Chrysopidae) from China, with description of two new species
FIGURE 4. Austrochrysa lihongyui sp. nov. (Xizang, Mêdog, Miri vill., holotype, male), male abdomen. A. Terminal segments, lateral view; B. Terminal segments, ventral view; C. Gonarcal complex, dorsal view; D. Tignum, dorsal view; E. Mediuncus, ventral view. cc callus cerci; ent entoprocessus; gcr gonocristae; gsac gonosaccus; gon gonarcus; mu mediuncus; S8 sternum 8; T8 tergum 8; T9+e tergum 9+ectoprocts.
Data from: Rapid comeback of males: evolution of male-killer suppression in a green lacewing population
Evolutionary theory predicts that the spread of cytoplasmic sex ratio distorters leads to the evolution of host nuclear suppressors, although there are extremely few empirical observations of this phenomenon. Here, we demonstrate that a nuclear suppressor of a cytoplasmic male killer has spread rapidly in a population of the green lacewing Mallada desjardinsi. An M. desjardinsi population, which was strongly female-biased in 2011 because of a high prevalence of the male-killing Spiroplasma endosymbiont, had a sex ratio near parity in 2016, despite a consistent Spiroplasma prevalence. Most of the offspring derived from individuals collected in 2016 had 1:1 sex ratios in subsequent generations. Contrastingly, all-female or female-biased broods appeared frequently from crossings of these female offspring with males derived from a laboratory line founded by individuals collected in 2011. These results suggest near-fixation of a nuclear suppressor against male killing in 2016 and reject the notion that a non-male-killing Spiroplasma variant has spread in the population. Consistently, no significant difference was detected in mitochondrial haplotype variation between 2011 and 2016. These findings, and earlier findings in the butterfly Hypolimnas bolina in Samoa, suggest that these quick events of male recovery occur more commonly than is generally appreciated.
FIGURE 93 in Systematics of the green lacewing tribe Ankylopterygini Navás, 1910 (Neuroptera: Chrysopidae: Chrysopinae) from China
FIGURE 93. ML tree of Ankylopterygini based on COI gene fragments (part). Numbers near each node are bootstrap value (%).
FIGURE 76 in Systematics of the green lacewing tribe Ankylopterygini Navás, 1910 (Neuroptera: Chrysopidae: Chrysopinae) from China
FIGURE 76. Signochrysa hainanus (Yang & Yang, 1991). A. Dorsal habitus; B. Head, frontal view; C. Head, lateral view; D. Thorax, dorsal. Scale bar: 5 mm (A), 1 mm (B–D).
FIGURE 92 in Systematics of the green lacewing tribe Ankylopterygini Navás, 1910 (Neuroptera: Chrysopidae: Chrysopinae) from China
FIGURE 92. ML tree of Ankylopterygini based on COI gene fragments (part). Numbers near each node are bootstrap value (%).
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