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Figure 5 in Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on molecular and morphological data

Figure 5. Mesosternum of adult Liviinae: A, Anomoterga scolopiae (Yang); B, Camarotoscena speciosa (Flor); C, Klyveria setinervis (Burckhardt); D, Livia junci (Schrank); E, Paurocephala robusta Mifsud and Burckhardt; F, Syntomoza magna (Kuwayama). Abbreviations: bas, basisternum; kat, katepisternum; pcx, precoxale; pss, pleurosternal suture; scs, sternocostal suture. Scales 0.1 mm.

Figure 7 in Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on molecular and morphological data

Figure 7. Metatibial apex of adult Liviidae: A, Strophingia cinereae Hodkinson; B, Aphorma lichenoides (Puton); C, Camarotoscena speciosa (Flor); D, Livia junci (Schrank); E, Diclidophlebia oceanica (Crawford); F, D. xuani (Messi); G, Haplaphalara dahli (Rübsaamen); H, Liella lanceomedia (Brown and Hodkinson); I, Klyveria setinervis (Burckhardt); J, Melanastera lucens (Burckhardt et al.); K, M. maculipennis (Brown and Hodkinson); L, Paurocephala sauteri Enderlein. Abbreviations: a, anterior view, l, lateral view, m, medial, p, posterior view. Scales 0.05 mm.

Figure 1 in Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on molecular and morphological data

Figure 1. Habitus images illustrating generic diversity within Liviinae: A, Anomoterga africana (Loginova); B, Aphorma lichenoides (Puton); C, Camarotoscena speciosa (Flor); D, Livia junci (Schrank); E, Syntomoza magna (Kuwayama); F, Diclidophlebia eastopi Vondráček; G, Haplaphalara dahli (Rübsaamen); H, Klyveria setinervis (Burckhardt); I, Liella cf. insolita (Mifsud and Burckhardt); J, Melanastera smithi (Burckhardt et al.); K, Paurocephala chonchaiensis Boselli; L, Woldaia nebulosa Brown and Hodkinson. Scales 1.0 mm.

Figure 4 in Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on molecular and morphological data

Figure 4. Metapostnotum of adult Liviinae (arrow pointing to tubercle, tooth, ridge or horn): A, Anomoterga hsenpinensis Fang and Yang; B, Livia vernalis Fitch; C, Melanastera smithi (Burckhardt et al.); D, Paurocephala chonchaiensis Boselli. Scales 0.1 mm.

Figure 3 in Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on molecular and morphological data

Figure 3. Head of adult Liviidae: A, Diclidophlebia xuani Messi; B, Syntomoza magna (Kuwayama); C, Anomoterga tahuata Klyver; D, Aphorma lichenoides (Puton); E, Camarotoscena speciosa (Flor); F, Livia junci (Schrank); G, Klyveria setinervis (Burckhardt); H, Paurocephala dayak Mifsud and Burckhardt. A, B, dorsal view; C–H, ventral view. Scales A, B = 0.1 mm; C–H = 0.1 mm.

Figure 11 in Phylogeny and classification of jumping plant lice of the subfamily Liviinae (Hemiptera: Psylloidea: Liviidae) based on molecular and morphological data

Figure 11. Phylogeny of the Liviidae showing strict consensus tree of the most parsimonious trees based on morphological data (character matrix in Supporting Information, File S2) and obtained with 'Traditional search' in TNT using equal weights. 'Unambiguous changes only' in WINCLADA was used to optimize the character states on the cladogram. Black circles represent synapomorphies, light circles homoplasies; numbers above circles refer to characters numbers, number below to the character states (Table 2). Host plants of Liviini: Malpigiales, Poa, Poales, Ran, Ranunculales; of Paurocephalini: representation of members of Malvales. Distribution: Afrotropics (Afr), Australasia (Aus), Indomalaya (Ind), Nearctic (Nea), Neotropics (Neo), Oceania (Oce), Palaearctic (Pal).

Fig. 4 a in Evolutionary pattern of the forewing shape in the Neotropical genus of jumping plant-lice (Hemiptera: Psylloidea: Russelliana)

Fig. 4 a Reconstructed ancestral shape of Russelliana forewing. b The forewing of Russelliana viscosae

Fig. 3 in Evolutionary pattern of the forewing shape in the Neotropical genus of jumping plant-lice (Hemiptera: Psylloidea: Russelliana)

Fig. 3 Scatter plot from the PCA showing scores on the first two PCs for the 43 species of Russelliana. Shape changes are shown by deformation grids associated with extreme values (− 0.20 and + 0.10 on the PC1, and

Fig. 7 in Evolutionary pattern of the forewing shape in the Neotropical genus of jumping plant-lice (Hemiptera: Psylloidea: Russelliana)

Fig. 7 Geographical distribution of Russelliana. a Verbenaceae- (5 spp.) and Solanaceae-feeders (6 spp.) from gr. 2. b Verbenaceae- (5 spp.) and Solanaceae-feeders (2 spp.) from gr. 1. c Asteraceae- (4 spp.) and Fabaceae-feeders (13 spp.). d R. solanicola, Rosaceae- (2 spp.) and Solanaceae-feeders (7 spp.) from gr. 3. The original map was taken from the Natural Earth, free vector, and raster map data @naturalearthdata.com; the geographical coordinates were entered using the Google Earth. Subdivision into morphostructural provinces of the Andean Region follows Ramos (2009)

Fig. 1 Simplified phylogeny for 43 in Evolutionary pattern of the forewing shape in the Neotropical genus of jumping plant-lice (Hemiptera: Psylloidea: Russelliana)

Fig. 1 Simplified phylogeny for 43 species of Russelliana. Three nodes with numbers (1–3) correspond to clades 1–3 with the strongest synapomorphic support. Numbers at branches are bootstrap values. Source tree is mentioned in the text

Fig. 6 Phylogeny for 43 in Evolutionary pattern of the forewing shape in the Neotropical genus of jumping plant-lice (Hemiptera: Psylloidea: Russelliana)

Fig. 6 Phylogeny for 43 species of Russelliana excluding characters on forewing morphology. Three nodes with numbers (1–3) correspond to clades 1–3 derived from the phylogenetic tree (Fig. 1). Numbers at branches are bootstrap values

Fig. 5 in Evolutionary pattern of the forewing shape in the Neotropical genus of jumping plant-lice (Hemiptera: Psylloidea: Russelliana)

Fig. 5 Scatter plot from the CVA of 41 species of Russelliana (R. nana and queirozae are excluded). Shape changes are shown by the wireframes associated with extreme values (− 30.0 and + 30.0 on the CV1, and − 40.0

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Figure 1 in Life cycle variation and adaptation in jumping plant lice (Insecta: Hemiptera: Psylloidea): a global synthesis

Figure 1. Dendrogram illustrating the level of correspondence among life history parameters measured across psyllid species. Note: similarity is measured by Euclidean distance; clustering is by average linkage.

FIG. 53 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIG. 53. Phylogenetic relationships of L ithrea and Schinus with deformations produced by Psylloidea:Ðirregularly deformed leaves by Tainarys spp.; open circle pit galls by members of the C. hermicitae group; open square pit galls by members of the C. rubra group; solid square closed galls by members of the C. rubra group.

FIG. 31 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIG. 31. Cladogram of all Calophya species (except for C. clavuligera and C. pallidula), with previous combinations (C= Calophya, P= Pelmatobrachia, M= Microceropsylla), provenance (EPal= East Palaearctic, Or= Oriental, NAm= North American, SAm = South American) and host genus (adult characters, cf. tables 4, 5).

FIGS 32 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIGS 32±36. Cladograms: (32) selected Calophya spp. (adult and larval characters, cf. tables 6, 7); (33) Calophya rubra group (except for C. ¯oricola) (cf. tables 8, 9); (34) Calophya hermicitae group (cf. tables 10, 11); (35) Rhinocolinae (cf. tables 12, 13); (36) Tainarys (cf. tables 14, 15).

FIGS 63, 64 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIGS 63, 64. Tainarys spp.: (63) SEM picture of adult T. inopinata; (64) deformations (arrow) of T. sordida on Schinus montanus.

FIG. 26 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIG. 26. Tainarys venata: A, male genitalia, in pro®le; B, paramere, inner face; C, distal segment of aedeagus; D, female genitalia, in pro®le.

FIG. 25 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIG. 25. Tainarys spp.: A±E, T. maculipectus; F±J, T. venata. A, I, forewing; B, male genitalia, in pro®le; C, female genitalia, in pro®le; D, paramere, inner face; E, distal segment of aedeagus; F, head, dorsal view; G, frons; H, egg; J, metacoxa.

FIG. 23. L in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships

FIG. 23. L eurolophus spp.: A±H, L. oriformae; I, L. vittatus. A, forewing; B, head, dorsal view; C, frons; D, male genitalia, in pro®le; E, paramere, inner face; F, distal segment of aedeagus; G, female genitalia, in pro®le; H, I, metacoxa.