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FIGURE 4 in Parasitism of Entedon costalis (Hymenoptera: Eulophidae) in Glocianus punctiger (Coleoptera: Curculionidae): an example of intentional discovery of the parasitoid-host association
FIGURE 4. The female of E. costalis on dandelion flowerstalk: A, B. Female probes through the wall of the flowerstalk; C, D. Oviposition of the same female; white arrow, hardened and oxidized dandelion sap in the place of the oviposition hole made by the host weevil female.
FIGURE 10. A, B in Parasitism of Entedon costalis (Hymenoptera: Eulophidae) in Glocianus punctiger (Coleoptera: Curculionidae): an example of intentional discovery of the parasitoid-host association
FIGURE 10. A, B, siblicide in first instars of E. costalis: A. Two larvae imaged when fighting; B. "Winner" and "loser" rivals; C. Enigmatic parasitoid (? braconid wasp) isolated from the egg of G. punctiger: D. Actively feeding first instar larva of E. costalis after adding a drop of ethanol (so the caudal bladder (cb) is condensed); fr, caudal formation.
FIGURE 7. A in Parasitism of Entedon costalis (Hymenoptera: Eulophidae) in Glocianus punctiger (Coleoptera: Curculionidae): an example of intentional discovery of the parasitoid-host association
FIGURE 7. A. Egg of E. costalis within the egg of G. punctiger; B. The egg of G. punctiger with melanized marks caused likely by the parasitoid's ovipositor; D, E. Parasitoid eggs with developing embryo from the host egg with many melanized marks; E. Pre-eclosion first-instar; ch, egg chorion; ec, embryonic cuticle; em, embryo; hm, host haemocytes; ms, median stripe.
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.
FIGS 38 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIGS 38± 49. (38) Taxon area cladogram (TAC) of the C. rubra group; (39) simpli®ed TAC of ®gure (38, 40) TAC of the C. hermicitae group; (41) TAC of Tainarys; (42) reduced area cladogram (RAC) of the C. rubra group; (43) RAC of the C. hermicitae group; (44) RAC of Tainarys; (45) TAC of the C. rubra group with three traceable vicariance events (TVE); (46) TAC of the C. hermicitae group with two TVE; (47) TAC of Tainarys without TVE; (48) diagram of vicariant events derived from cladogram of the C. rubra group (®gure 45); (49) diagram of vicariant events derived from cladogram of the C. hermicitae group (®gure 46).
FIG. 5 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 5. Calophya spp.: A±F, C. duvauae; G±K, C. ¯oricola. A, G, forewing; B, H, female genitalia, in pro®le; C, spermatheca; D, J, distal segment of aedeagus; E, K, male genitalia, in pro®le; F, I, paramere, inner face.
FIG. 8 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 8. Calophya spp.: A±F, C. patagonica; G±L, C. rubra. A, G, forewing; B, K, paramere, inner face; C, H, spermatheca; D, I, female genitalia, in pro®le; E, J, male genitalia, in pro®le; F, L, distal segment of aedeagus.
FIG. 9 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 9. Calophya spp.: A±E, G, C. schini; F, H±K, C. scrobicola. A, F, forewing; B, K, distal segment of aedeagus; C, spermatheca; D, H, female genitalia, in pro®le; E, J, paramere, inner face; G, I, male genitalia, in pro®le.
FIG. 2 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 2. Canonical variate analysis of 50 female specimens measured in the C. rubra group. (a) Distribution of eigenvalues among the discriminant axes; (b) plot of the specimens projected on discriminant axes 1 and 2; (c) correlation circle of variables projected on axes 1 and 2; (d) plot of the specimens projected on axes 3 and 4; (e) correlation circle of variables projected on axes 3 and 4. Species and variable codes as in ®gure 1.
FIG. 7 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 7. Calophya spp.: A±F, C. mammif ex; G±K, C. orbicola. A, H, forewing; B, spermatheca; C, K, paramere, inner face; D, G, distal segment of aedeagus; E, I, female genitalia, in pro®le; F, J, male genitalia, in pro®le.
FIG. 4 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 4. Calophya spp.: A±E, C. catillicola; F±K, C. clausa. A, F, forewing; B, H, female genitalia, in pro®le; C, I, male genitalia, in pro®le; D, K, distal segment of aedeagus; E, J, paramere, inner face; G, spermatheca.
FIG. 1 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 1. Canonical variate analysis of 44 male specimens measured in the C. rubra group. (a) Distribution of eigenvalues among the discriminant axes; (b) plot of the specimens projected on discriminant axes 1 and 2; (c) correlation circle of variables projected on axes 1 and 2; (d) plot of the specimens projected on axes 3 and 4; (e) correlation circle of variables projected on axes 3 and 4. Species codes as follows: 1 = C. andina, 2 = C. clausa, 3 = C. ¯oricola, 4 = C. gallifex, 5= C. mammif ex, 6 = C. orbicola, 7= C. patagonica, 8= C. rubra, 9= C. schini, 10 = C. scrobicola. Codes of variables (measurements) as detailed in the methods.
FIG. 10 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 10. Calophya terebinthifolii: A, forewing; B, distal segment of aedeagus; C, spermatheca; D, female genitalia, in pro®le; E, male genitalia, in pro®le; F, paramere, inner face.
FIG. 3 in The jumping plant-lice (Hemiptera, Psylloidea) associated with Schinus (Anacardiaceae): systematics, biogeography and host plant relationships
FIG. 3. Calophya andina: A, forewing; B, C, female genitalia, in pro®le; D, E, spermatheca; F, G, male genitalia, in pro®le; H, I, paramere, inner face; J, K, distal segment of aedeagus.
ScienceDex guides
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.