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894 results for “Coccoidea”
Fig. 4 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa
Fig. 4. Hemilecanium cedrelus Hodgson, sp. n., female 2nd-instyar nymph. For lettering, see Figs 1 & 2, but also where 3rd = position of dorsal tubercles on pharate 3rd-instar nymph.
Fig. 3 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa
Fig. 3. Hemilecanium cedrelus Hodgson, sp. n., female 3rd- instar nymph. For lettering, see Figs 1 & 2, but where scar = position of scars left by dorsal tubercles of 2nd-instar nymph.
Fig. 2 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa
Fig. 2. Hemilecanium cedrelus Hodgson, sp. n., adult female. For lettering, see Fig. 1, but also where B = dorsal tubercle; E = preopercular pore; J = marginal seta and J 1 = marginal seta on anal lobe; K = stigmatic spines; P = tubular ducts; and scars = scars showing position of dorsal tubercles of 3rd-instar nymph.
Fig. 1 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa
Fig. 1. Sterculicoccus tafoensis Hodgson, sp. n., adult female. Where: A = dorsal setae; C = dorsal microductule; D = dorsal simple porte; F = dorsal view of anal plates; G = ventral view of anal plates; H = microridges on dorsal surface of anal plate; J = marginal seta; L = pregenital disc-pore; M = spiracular disc-pore; N = ventral microduct; P = larger ventral tubular duct; Q = smaller ventral tubular duct; R = antenna; S = claw, and T = ventral setae.
Fig. 5 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa
Fig. 5. Hemilecanium cedrelus Hodgson, sp. n., 1st-instar nymph (sex unknown). For lettering, see Figs 1 & 2, but where E = dorsal trilocular pore; L =dorsal protuberances, and H = tibio-tarsal articulation with microspines.
Figure 5 in Population dynamics of the gall inducer Eriogallococcus isaias (Hemiptera: Coccoidea: Eriococcidae) on Pseudobombax grandiflorum (Malvaceae)
Figure 5. Phenological cycle of the galls induced by Eriogallococcus isaias on Pseudobombax grandiflorum from August to December 2008.
Figures 2 in The species of Astymachus Howard (Hymenoptera: Encyrtidae)ı potentially important parasitoids of Aclerdidae (Hemiptera: Coccoidea) associated with grasses (Poaceae)ı with descriptions of three new species
Figures 2. Astymachus saccharum sp. nov.: (a) head (holotype); (b) antenna ♀ (holotype); (c) apex of fore wing venation (paratype); (d) fore wing (paratype). Astymachus felix Singh and Hayat: (e) apex of fore wing venation. Astymachus phainae Sugonjaev: (f) fore wing; (g) apex of fore wing venation. Astymachus lasallei sp. nov. (holotype) (h) antenna ♀; (i) head; (j) fore wing; (k) discal setae below marginal vein, enlarged (differential interference contrast); (l) apex of fore wing venation. Asymachus phragmitis Trjapitzin: (m) head; (n) antenna ♀. (Figures e-g courtesy of Mohammad Hayat).
Figures 3 in The species of Astymachus Howard (Hymenoptera: Encyrtidae)ı potentially important parasitoids of Aclerdidae (Hemiptera: Coccoidea) associated with grasses (Poaceae)ı with descriptions of three new species
Figures 3. Astymachus phragmitis Trjapitzin: (a) antenna ♂; (b) fore wing; (c) apex of fore wing venation. Astymachus japonicus Howard: (d) head; (e) antenna ♀; (f) antenna ♂; (g) apex of fore wing venation; (h) fore wing. Astymachus srilankae sp. nov. (holotype): (i) head; (j) antenna ♀; (k) antenna ♂; (l) fore wing; (m) apex of fore wing venation.
FIGURE 2 in Description of a new species of Ovaticoccus Kloet (Hemiptera: Coccoidea, Eriococcidae) from Belize, with remarkably large hind coxae and causing leafcurl galls
FIGURE 2. Ovaticoccus amplicoxae sp. nov., unmounted adult female in alcohol, with large hind coxa prominent.
FIGURE 1. A in A new hypogeal species of Oregmopyga Hoy (Hemiptera: Coccoidea: Eriococcidae) from southern California, U. S. A., and a key to species of the genus
FIGURE 1. A, Encasement of Oregmopyga viscosa Kondo sp. nov. showing root fibers and imprinted abdominal segmentation; B, Dorsal view of insect, showing bare dorsum of shiny red color and abdominal segmentation; C, Live specimen inside encasement with venter covered with powdery wax.
FIGURE 7 in Hodgson, C. et al. (2008) Phenacoccus solenopsis Tinsley (Sternorrhyncha: Coccoidea: Pseudococci- dae), an invasive mealybug damaging cotton in Pakistan and India, with a discussion on seasonal morphological variation. Zootaxa, 1913, 1-35.
FIGURE 7. First-instar nymph of Phenacoccus solenopsis Tinsley from Pakistan and India. Labels as in Fig. 1.
Figure 52. Pseudococcidae spp. A in The mealybugs (Hemiptera: Coccoidea: Pseudococcidae) of Egypt
Figure 52. Pseudococcidae spp. A) Misericoccus salsolilcola (after Priesner and Hosny 1935). B) Misericoccus imperatae (after Hall 1923). C) Antonina panici (after Hall 1925). D) Phenacoccus gypsophilae (after Hall 1927c).
Figure 1 in The mealybugs (Hemiptera: Coccoidea: Pseudococcidae) of Egypt
Figure 1. Morphological terms used in Pseudococcidae. A) Antennae. B) Hind leg—translucent pores (tp), claw denticles (cd), tarsal denticles (td). C) Habitus—cephalothoracic cerarii 1–10 (c1–c10), abdominal cerarii 1–8 (ac1–ac8). D) Cerarii. E) Pores—multilocular pore (ml), quinquelocular pore (qp), trilocular pore (tl), discoidal pore (dp). F) Ducts— oral rim tubular duct (or), oral collar tubular duct (oc), crateriform duct (cf), Ferrisia-type duct (fd). G) Anal lobe, dorsal. H) Anal ring. I) Anal lobe, ventral. Source: modified from Williams (2004).
Figure 5 in Characterization of the first mitochondrial genome of Aclerdidae (Hemiptera: Coccoidea) with a novel gene arrangement
Figure 5. Sternorrhyncha phylogenetic tree inferred from mitochondrial genome matrix. The phylogenetic tree were reconstruct using Bayesian inference method. Numbers at the nodes indicate Bayesian posterior probabilities.
Figure 4 in Characterization of the first mitochondrial genome of Aclerdidae (Hemiptera: Coccoidea) with a novel gene arrangement
Figure 4. Comparison of the mitochondrial gene arrangement among Nipponaclerda biwakoensis, ancestral insect, other representative species of Psyllidae, Aphididae and Aleyrodidae and four public Coccocidea species.
Figure 2 in Characterization of the first mitochondrial genome of Aclerdidae (Hemiptera: Coccoidea) with a novel gene arrangement
Figure 2. The codon number and relative synonymous codon usage (RSCU) in the Nipponaclerda biwakoensis mitochondrial genome.
Figure 1 in Characterization of the first mitochondrial genome of Aclerdidae (Hemiptera: Coccoidea) with a novel gene arrangement
Figure 1. Gene map of the Nipponaclerda biwakoensis mitochondrial genome. Arrows indicate the orientation of gene transcription. The inner circles show G+C content.
Figure 3 in Characterization of the first mitochondrial genome of Aclerdidae (Hemiptera: Coccoidea) with a novel gene arrangement
Figure 3. Predicted secondary structures of the 17 detected tRNA genes of Nipponaclerda biwakoensis mitochondrial genome. Watson–Crick pairs is indicated by lines, wobble GU pairs is indicated by dots and other noncanonical pairs is indicated by circles.
Fig. 1 in Hymenopteran parasitoids associated with scale insects (Hemiptera: Coccoidea) in tropical fruit trees in the eastern Amazon, Brazil
Fig. 1. Interactions between species of scale insects and parasitoids with the total number of interactions with each species of host plant (Jun 2014 to Aug 2015) at Maranhão Island, Maranhão, Brazil.
Fig. 8 in Description Of New Genera And Species In The Tribe Rhizoecini (Homoptera, Coccoidea, Pseudococcidae)
Fig. 8. Coccidella globocula (HAMBLETON, 1946) (modified after WILLIAMS & GRANARA DE WILLINK 1992)
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.