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zenodo28/100

Figure 4 from: Pujade-Villar J, Wang Y, Zhang W, Mata-Casanova N, Lobato-Vila I, Dénes A-L, László Z (2020) A new Diplolepis Geoffroy (Hymenoptera, Cynipidae, Diplolepidini) species from China: a rare example of a rose gall-inducer of economic significance. ZooKeys 904: 131-146. https://doi.org/10.3897/zookeys.904.46547

Figure 4 a forewing of D. flaviabdomenisb forewing of D. hunanensisc forewing of D. minoriabdomenis, and d forewing of D. nr japonicae head in frontal view of D. nr japonica (reused from Wang et al. 2013) f head in dorsal view of D. nr japonica (reused from Wang et al. 2013) g head in frontal view of D. hunanensish lateral mesosoma of D. minoriabdomenisi mesoscutum of D. nr japonica.

opencc-by-4.0Jan 2020View details →
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Figure 5 from: Pujade-Villar J, Wang Y, Zhang W, Mata-Casanova N, Lobato-Vila I, Dénes A-L, László Z (2020) A new Diplolepis Geoffroy (Hymenoptera, Cynipidae, Diplolepidini) species from China: a rare example of a rose gall-inducer of economic significance. ZooKeys 904: 131-146. https://doi.org/10.3897/zookeys.904.46547

Figure 5 Bayesian inference (BI) tree of the Diplolepis species that have available mitochondrial COI sequences. Numbers on the branches represent posterior probabilities (PP).

opencc-by-4.0Jan 2020View details →
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Figure 2 from: Pujade-Villar J, Wang Y, Zhang W, Mata-Casanova N, Lobato-Vila I, Dénes A-L, László Z (2020) A new Diplolepis Geoffroy (Hymenoptera, Cynipidae, Diplolepidini) species from China: a rare example of a rose gall-inducer of economic significance. ZooKeys 904: 131-146. https://doi.org/10.3897/zookeys.904.46547

Figure 2 Diplolepis abei Pujade-Villar & Wang ♀ sp. nov. a–b galls c dissected gall with last instar larva d forewing e lateral and ventral view of the 3rd instar larva f lateral and ventral view of the last instar larva g lateral habitus.

opencc-by-4.0Jan 2020View details →
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Figure 1 from: Pujade-Villar J, Wang Y, Zhang W, Mata-Casanova N, Lobato-Vila I, Dénes A-L, László Z (2020) A new Diplolepis Geoffroy (Hymenoptera, Cynipidae, Diplolepidini) species from China: a rare example of a rose gall-inducer of economic significance. ZooKeys 904: 131-146. https://doi.org/10.3897/zookeys.904.46547

Figure 1 Diplolepis abei Pujade-Villar & Wang ♀ sp. nov. a head in frontal view b genae in dorsal view c antenna d mesosoma in lateral view e mesosoma in dorsal view f mesosoma in dorso-lateral view g propodeum h metasoma in lateral view.

opencc-by-4.0Jan 2020View details →
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Figure 5 in Three new species of gall-forming psyllids (Hemiptera: Psylloidea) from Papua New Guinea, with new records and notes on related species

Figure 5. Adult comparison of Cornegenapsylla allophyli Malenovský and Percy, sp. nov. (A, D, E) and Cornegenapsylla sinica Yang and Li (B, C, F). (A, B) Forewings: (A) C. allophyli, (B) C. sinica; (C, D) heads: (C) C. sinica, (D) C. allophyli; (E, F) male terminalia: (E) C. allophyli, (F) C. sinica. Comparison of adult male terminalia in specimens of Pauropsylla triozoptera Crawford (G, left to right): from Papua New Guinea, Philippines, with inset schematic of gall phenotypes; (H) 5th instar circumanal pore area of P. triozoptera from Taiwan. Comparison of adult male terminalia in specimens Pauropsylla udei Rübsaamen (I, left to right): from Papua New Guinea, Hong Kong, Bangladesh, Philippines, with inset schematic of gall phenotypes.

opencc-by-4.0Sep 2015View details →
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Figure 6 in Three new species of gall-forming psyllids (Hemiptera: Psylloidea) from Papua New Guinea, with new records and notes on related species

Figure 6. Adult Cornegenapsylla allophyli Malenovský and Percy, sp. nov. (A) Forewings and hindwing, upper forewing imaged with reflected light and lower with transmitted light; (B) hind leg; (C) thorax dorsum; (D) clypeus and proboscis; (E) antenna, terminal two segments (inset); (F) antennal rhinaria on 4th (lower), 5th (middle) and 6th (upper) segments; (G) head, lateral (left), ventral (middle) and lateral showing reduced but distinct genal tubercles (right); (H) male terminalia; (I) paramere (inner surface); (J) distal aedeagus segment; (K) female terminalia, circumanal ring (inset); (L) ovipositor.

opencc-by-4.0Sep 2015View details →
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Figure 2 in Three new species of gall-forming psyllids (Hemiptera: Psylloidea) from Papua New Guinea, with new records and notes on related species

Figure 2. Immatures, Trioza incrustata Percy, sp. nov. (A–F), and Trioza grallata Percy, sp. nov. (G–K). (A–D) 5th instar; (B) outline illustrating distinct pattern on dorsal surface; (C) antenna and tarsi; (D) circumanal ring; (E) 4th instar; (F) 2nd instar; (G–I) 5th instar; (H) antenna and tarsi; (I) circumanal ring; (J) 3rd instar; (K) 1st instar.

opencc-by-4.0Sep 2015View details →
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Figure 1 in Three new species of gall-forming psyllids (Hemiptera: Psylloidea) from Papua New Guinea, with new records and notes on related species

Figure 1. Adult Trioza incrustata Percy, sp. nov. (A) Forewing and hindwing (inset); (B, C) head and antenna; (D) clypeus; (E) proboscis; (F) thorax dorsum; (G) hind leg; (H) male terminalia; (I) paramere (inner surface); (J) distal aedeagus segment; (K) female terminalia; (L) ovipositor.

opencc-by-4.0Sep 2015View details →
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Figure 3 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 3. Prodorsal region, gnathosoma and legs of Aceria rhodiolae females from (B‒D) Nunavik, QC (Canada); (E) Labrador, NFLD (Canada); (F,G) Russia; and (H) Italy. (A) Line drawings, (B,C) scanning electron micrographs, (D) confocal light scanning microscopy, (E‒H) differential interference contrast light microscopy. Inset of (A) shows enlargement of empodia of leg I, and insets in (B) show enlargements of opisthosomal microtubercles and of dorsal gnathosoma. Notations in (A): ad, admedian line; sub II, submedian line II; tr, trochanter; so, solenidion; and others indicate setae of legs (femur to tarsus) and palp (coxal and genual setae). Arrows in (C) and (G) indicate characteristic ridges present in most (a) and some (b) specimens, respectively. The scale for images D‒H is indicated on (A) and the scale for (C) is the same as that on (B).

opencc-by-4.0Sep 2015View details →
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Figure 7 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 7. Prodorsal region and genital coverflap (inset) of Aceria destructor female (differential interference contrast light microscopy). Arrows indicate characteristic ridges discernible in most (a) and some (b) specimens, respectively.

opencc-by-4.0Sep 2015View details →
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Figure 6 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 6. Internal genitalia of Aceria rhodiolae female (A,D) and external and internal genitalia of male (B,C,E,F). (A) Line drawing based on both Russian and Nunavik females; differential interference contrast light microscopy (B,D,E) and confocal light scanning microscopy (C,F) from a Russian female (D) and Labrador males (B,C,E,F). aga, anterior genital apodeme; ch, genital chamber; ded, distal ejaculatory duct; eu, eugenital setae; gc, walls (collapsed) of genital channel (longitudinal bridge); oa, oblique apodeme; ped, proximal ejaculatory duct; sd, spermathecal duct; sp, spermatheca; ts, putative testis; vd, vasa deferentia. Figures A and D are on the same scale, and B‒C and E‒F are on the same scale.

opencc-by-4.0Sep 2015View details →
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Figure 2 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 2. Aceria rhodiolae habitus. (A) Many (mostly adult) individuals under dissecting scope. (B) Adult female ventrolateral view (scanning electron micrograph) and (C) dorsolateral view (differential interference contrast light microscopy). Scale on (B) also applies to (C). The large size of female in (C) is in part due to some flattening of that specimen during the slide-mounting process. ch, cheliceral stylets; and other notations indicate setae of prodorsal shield and opisthosoma.

opencc-by-4.0Sep 2015View details →
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Figure 9 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 9. Salidroside and rosavins contents in Rhodiola rosea plants that were ungalled (healthy, n = 94) and galled (deformed, n = 60) by Aceria rhodiolae. Error bars on y-axis are standard deviations.

opencc-by-4.0Sep 2015View details →
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Figure 4 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 4. Legs of Aceria rhodiolae female (scanning electron micrographs), from Nunavik (Canada). (A) Legs I (left) and II (right); (B) legs I (left) and II (right). Arrows show ridges (r) on tibia I and II, and some of the spinules on the anterior margins of trochanter, femur, genu and tibia.

opencc-by-4.0Sep 2015View details →
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Figure 2 from: Tung G-S, Liao Y-C, Burckhardt D, Yang M-M (2020) Trioza turouguei sp. nov. (Hemiptera, Psylloidea, Triozidae), a new psyllid species from Taiwan inducing pea-shaped stem galls on Cinnamomum osmophloeum (Lauraceae), with notes on its galling biology. ZooKeys 958: 91-106. https://doi.org/10.3897/zookeys.958.52977

Figure 2 Trioza turouguei sp. nov. A head B antenna C hind leg D forewing. Scale bars: 0.1 mm (A, B, C); 1 mm (D).

opencc-by-4.0Aug 2020View details →
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Figure 1 from: Tung G-S, Liao Y-C, Burckhardt D, Yang M-M (2020) Trioza turouguei sp. nov. (Hemiptera, Psylloidea, Triozidae), a new psyllid species from Taiwan inducing pea-shaped stem galls on Cinnamomum osmophloeum (Lauraceae), with notes on its galling biology. ZooKeys 958: 91-106. https://doi.org/10.3897/zookeys.958.52977

Figure 1 Adults of Trioza turouguei sp. nov. A male, dorsal view B male, lateral view C female, dorsal view D female, lateral view. Scale bars: 1 mm.

opencc-by-4.0Aug 2020View details →
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Figure 5 from: Tung G-S, Liao Y-C, Burckhardt D, Yang M-M (2020) Trioza turouguei sp. nov. (Hemiptera, Psylloidea, Triozidae), a new psyllid species from Taiwan inducing pea-shaped stem galls on Cinnamomum osmophloeum (Lauraceae), with notes on its galling biology. ZooKeys 958: 91-106. https://doi.org/10.3897/zookeys.958.52977

Figure 5 Trioza turouguei sp. nov. on its host plant, Cinnamomum osmophloeum Kanehira A male B female C pea-like galls on stem D fifth instar immature in a gall.

opencc-by-4.0Aug 2020View details →
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Figure 4 from: Tung G-S, Liao Y-C, Burckhardt D, Yang M-M (2020) Trioza turouguei sp. nov. (Hemiptera, Psylloidea, Triozidae), a new psyllid species from Taiwan inducing pea-shaped stem galls on Cinnamomum osmophloeum (Lauraceae), with notes on its galling biology. ZooKeys 958: 91-106. https://doi.org/10.3897/zookeys.958.52977

Figure 4 Fifth instar immature of Trioza turouguei sp. nov. A habitus B marginal sectasetae of head C marginal sectasetae of forewing pad D marginal sectasetae of hindwing pad E marginal sectasetae of caudal plate F tarsal arolium G antenna H circumanal ring. Scale bars: 0.1 mm.

opencc-by-4.0Aug 2020View details →
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Figure 3 from: Tung G-S, Liao Y-C, Burckhardt D, Yang M-M (2020) Trioza turouguei sp. nov. (Hemiptera, Psylloidea, Triozidae), a new psyllid species from Taiwan inducing pea-shaped stem galls on Cinnamomum osmophloeum (Lauraceae), with notes on its galling biology. ZooKeys 958: 91-106. https://doi.org/10.3897/zookeys.958.52977

Figure 3 Terminalia of Trioza turouguei sp. nov. in lateral view A male terminalia B paramere, inner surface C distal portion of aedeagus D female terminalia E detail of female circumanal ring. Scale bars: 0.2 mm (A, D, E); 0.1 mm (B, C).

opencc-by-4.0Aug 2020View details →
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Figure 9 in Description, molecular phylogeny, and natural history of a new kleptoparasitic species of gelechiid moth (Lepidoptera) associated with Melastomataceae galls in Brazil

Figure 9. Bayesian inference tree for the new genus, based on 621 bp of the mitochondrial cytochrome oxidase c subunit I gene (CO-I). Numbers above branches indicate support values> 0.8/60 for Bayesian posterior probability (BPP)/bootstrap – for maximum likelihood (ML); those located below represent the percentage of evolutionary divergence between clades. Asterisk indicates support <0.80/60 for BPP and ML, respectively.

opencc-by-4.0Feb 2015View details →

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