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Figure 5 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 5 Morphology of Andescecidiumparrai last larval instar under scanning electron microscopy. A, B head, lateral (A) and antero-dorsal (B) views C stemmata, lateral D antenna, lateral E labium, lateral F maxilla, lateral G thorax, lateral H first abdominal spiracle, lateral I detail of second abdominal segment, showing aligned setae (arrow indicates spiracle), lateral J callus of second abdominal tergum, latero-dorsal K last abdominal segments, postero-lateral L ventral lobe of tenth abdominal segment (enlarged area marked with rectangle in K). Scale bars: 150 µm (A, B), 30 µm (C, L), 20 µm (D, E), 50 µm (F, I), 300 µm (G), 10 µm (H), 100 µm (J, K).

Figure 9 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 9 Olierasaizi adult morphology, under light microscopy (paratypes). A fore and hindwing venation, dorsal view B schematic representation of female oviscapt cone, lateral (asterisk indicates the distal end of internal dorsal crest; closed and open arrows point to the anterior ends of anterior and posterior left apophyses, respectively) C ovipositor tip in detail, lateral (enlarged area marked by rectangle in B) D male genitalia, ventral (phallus and juxta omitted) E distal section of right valva pectinifer in detail (enlarged area marked by rectangle in D) F phallus, ventral G juxta, ventral. Scale bars: 1 mm (A), 200 µm (B), 10 µm (C), 100 µm (D, F, G), 30 µm (E).

Figure 3 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 3 Andescecidiumparrai adult morphology under light microscopy (LMCI 218-03). A head, anterior view B metathoracic furcasternum, posterior (closed arrow points to left furcal apophysis) C fore-, median- and hindlegs, from left to right, respectively D female genitalia, dorsal (open and closed arrows point to the anterior ends of left anterior and posterior right apophyses, respectively) E distal portion of female genitalia in detail, lateral (enlarged area marked by rectangle in D; closed arrow points to the ovipositor tip; asterisk identifies oviscapt seen by transparency; bracket indicates distal margin of sternum eight). Scale bars: 0.3 mm (A, B), 1 mm (C), 0.2 mm (D, E).

Figure 2 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 2 Pinned-dried males (holotypes, left) and females (paratypes, right) of Andescecidiumparrai (A, B) and Olierasaizi (C, D), dorsal view. Scale bars: 2 mm (A, B), 1 mm (C, D).

Figure 8 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 8 Natural history of Andescecidiumparrai on Schinuspolygamus. A host-plant habitat at Cuesta La Dormida, intersection Til-Til/Valparaíso, beginning of road to Rungue, Chile, 33°3'42"S, 71°0'35"W (seta on the horizon points to the El Altar mountain, Metropolitan region) B young, developing galls, lateral C mature gall, lateral, with pedunculus (indicated by arrow) in detail in the upper right corner D, E old, empty galls under lateral and posterior views, respectively (setae point to apical open). Scale bars: 4 mm (B, C, E), 3 mm (D).

Figure 15 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 15 Geographic distribution of Andescecidiumparrai (green circles) and Olierasaizi (blue circles) in central Chile. Regions are indicated by Roman numbers except for the Metropolitan (RM). Localities are indicated by cardinal numbers: 1 Parque Nacional La Campana 2 Cuesta La Dormida 3 Til-Til/Hungue 4 Cuesta Barriga 5 Cajón del Maipo 6 Curicó 7 San Clemente 8 Cruce Nebuco, and 9 Recinto; for a complete description of corresponding localities, see list of specimens examined.

Figure 4 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090

Figure 4 Infected host organs and spore images of R.xanthophloeae (A–H), R.natalensis (I), R. evansii (J) and R.macowaniana (K) A Infected individual of V.xanthophloea. Leaves were prematurely shed in comparison with uninfected trees B Telia on leaflets of V.xanthophloeaC SEM of an aeciospore showing scattered germpores D SEM of an urediniospore E Urediniospores seen in LM F SEM view of a teliospore of R.xanthophloeae. The arrows indicate irregularly arranged verrucose ornamentations G Telium of R.xanthophloeae seen in SEM H LM view of a teliospore. The arrow indicates irregularly arranged verrucose ornamentations I Teliospores of R.natalensis with long pedicels J SEM picture of median section of a teliospore of R.evansii. Arrows indicate 2-celled probasidial cells K LM picture of teliospores of R.macowaniana. Scale bars: 1 mm (B), 4 μm (C), 2 μm (D), 20 μm (E), 20 μm (F–H, J–K), 40 μm (I).

Figure 3 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090

Figure 3 Radarchart of mean values of the morphological investigations of teliospore characteristics of Raveneliamacowaniana originated from Vachelliakarroo (red), V.natalitia (green) and R.xanthophloeae on V.xanthophloea (blue). Numbers on y-axis represent the respective minimum and maximum values. This radarchart reveals the morphological differences between R.macowaniana and R.xanthophloeae.

Figure 1 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090

Figure 1 Phylogenetic reconstruction of Ravenelia species on different Vachellia hosts A Maximum likelihood tree with 1000 bootstrap repeats based on combined nrITS and LSU rDNA sequence data. Bootstrap values below 75 are not shown. Three highly supported groups represent R.evansii, R.macowaniana and R.xanthophloeae sp. nov., respectively. Specimens that originated from formerly unreported host species are highlighted in bold B Parsimony network analysis based on the same dataset as in the ML-analysis. Each line represents one base substitution while small circles represent intermediate but missing sequences. Numbers next to lines indicate the positions of the substitutions in the alignment. Sequences in rectangular boxes were inferred as ancestral by this analysis.

Figure 2 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090

Figure 2 Biplots of a principal component analysis (PCA) of six teliospore characteristics of specimens of ARaveneliamacowaniana originating from Vachelliakarroo (red) and V.natalitia (green) and B in comparison with R.xanthophloeae sp. nov. collected from V.xanthophloea (blue) C, D represent R.evansii originating from seven distinct Vachellia species. Each dot represents an individual teliospore for which mean values of multiple measurements of all six defined morphological characteristics were calculated. Each colour represents the host species of the individual rust specimen. In D only spore representatives collected from V.borleae, V.exuvialis and V.davyi were highlighted to gain better visibility.

Figure 9 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 9 - Natural history of Neosphecia cecidogena on Cayaponia pilosa A host plant at the type locality B young fruit, lateral C fully developed gall on axillary region, lateral D, E basal portion of median-sized gall sectioned transversally, showing yellowish nutritive tissue (pointed by closed arrows) (D) longitudinally sectioned medium-sized galls, showing larval feeding scars on nutritive tissue (some are indicated by open arrows) F longitudinally sectioned mature gall, with last instar larva (asterisk) inside (closed and open arrows indicate frass and operculum, respectively) G transversally sectioned, senescent gall showing detached operculum (indicated by seta) and internal wall covered by silk H longitudinally sectioned senescent gall showing internal silk covering (proximal limit pointed by closed arrow) I senescent, overwintering gall, lateral (seta indicates direction of adult emergence) J distal portion of senescent gall, showing pupal exuvium left partially protruded after adult emergence (marked with asterisk). Scale bars: 2 mm (G, H); 3mm (D–F); 4mm (J); 6 mm (I); 9 mm (C); 1 cm (B); 9 cm (A).

Figure 8 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 8 - Neosphecia cecidogena pupal morphology under scanning electron microscopy A, C head, ventral and lateral views, respectively B clipeal seta in detail D third to sixth abdominal segments, lateral E fourth abdominal spiracle, lateral F spines of fourth abdominal segment in detail, lateral G last abdominal segments, posterior H spine of last abdominal segment, mesal. Scale bars: 40 µm (H); 50 µm (B, E); 100 µm (F); 200 µm (C, G); 0.4 mm (A); 0.5 mm (D), respectively.

Figure 6 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 6 - Morphology of Neosphecia cecidogena last larval instar under scanning electron microscopy A head, antero-dorsal view B antenna, anterior C stemmata, lateral D maxillae and labium, ventral E spineret, lateral F prothoracic shield, dorsal G meso- and metathoracic segments, dorsal H prothoracic leg, posterior I tarsal claw in detail, posterior J prothoracic spiracle, lateral K second to fourth abdominal segments, lateral L abdominal callus in detail, ventral. Scale bars: 20 µm (E, I, J); 40 µm (B), 100 µm (C, D, H, L); 0.5 mm (A, G, K).

Figure 5 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 5 - Neosphecia cecidogena last larval instar under light microscopy A cephalic chaetotaxy, frontal view B thoracic and abdominal chaetotaxy, lateral C, D head in detail, anterior and lateral, respectively. E last abdominal segments in detail, dorsal. Scale bars: 200 µm (A, D); 0.4 mm (E); 0.5 mm (C); 1 mm (B).

Figure 3 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 3 - Neosphecia cecidogena genitalia morphology under light microscopy A male (LMCI 319-84), general, ventral view (unrolled preparation, sensu Pitkin 1986; aedeagus omitted) B right half of the tegumen-uncus complex, mesal (pointed by closed arrow in A asterisk indicates anal tube) C distal portion of left valva in detail (enlarged area marked with a rectangle in A), ventral D aedeagus, lateral E female (LMCI 306-19), general, ventral (open arrow points to missing distal portion of the right anterior apophysis, broken off during preparation). Scale bars = 0.1 mm (B–D); 0.3 mm (A, E).

Figure 2 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 2 - Pinned-dried Neosphecia cecidogena adults, with corresponding heads in detail A–D male (holotype, LMCI 319-83) E–H female (paratype, LMCI 319-85); dorsal (A, C, E, G), ventral (B, F) and lateral (D, H) views. Scale bars = 0.5mm (C, D, G, H); 4mm (A, B, E, F).

Figure 4 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 4 - Egg of Neosphecia cecidogena under scanning electron microscopy A general view B chorion in detail C micropyle area. Scale bars: 100, 15, 20 µm, respectively.

Figure 1 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 1 - Maximum likelihood consensus tree of Neosphecia cecidogena (LMCI 263-33) and related Melittiini taxa. The monophyly and relationships were inferred based on 668 base pairs of cytochrome oxidase subunit gene I (COI) sequences (using six species of Melittia , one from Synanthedon and Carmenta from databases; the later genera of the related subfamily Synanthedonini were surveyed as outgroups). Numbers above branches indicate statistical support (bootstrap values).

Figure 7 from: Moreira GRP, Gorbunov OG, Fochezato J, Gonçalves GL (2019) A peculiar new species of gall-inducing, clearwing moth (Lepidoptera, Sesiidae) associated with Cayaponia in the Atlantic Forest. ZooKeys 866: 39-63. https://doi.org/10.3897/zookeys.866.34202

Figure 7 - Neosphecia cecidogena pupa under light microscopy, in dorsal (A), ventral (B) and lateral (C) views. Scale bar:1 mm.