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Fig. 4 in Evaluating categories of resistance in soybean genotypes from the United States and Brazil to Aphis glycines (Hemiptera: Aphididae)
Fig. 4. Cumulative aphid-days (CAD) for soybean genotypes infested with Aphis glycines at V1 and V3 stages (23 ± 3 °C; 60 ± 10% RH; 16:8 h L:D photoperiod).
Fig. 3 in Evaluating categories of resistance in soybean genotypes from the United States and Brazil to Aphis glycines (Hemiptera: Aphididae)
Fig. 3. Number (mean ± SE) of Aphis glycines individuals on 7 soybean genotypes 24 h afer infestation (23 ± 3 °C; 60 ± 10% RH; 16:8 h L:D photoperiod). Means with the same lower case letter do not differ by Fisher's LSD test (P> 0.05). (F = 1.74; df = 6; P = 0.0110).
Fig. 2 in Evaluating categories of resistance in soybean genotypes from the United States and Brazil to Aphis glycines (Hemiptera: Aphididae)
Fig. 2. Number (mean ± SE) of Aphis glycines individuals on KS4202 plants 24 h afer infestation (23 ± 3 °C; 60 ± 10% RH; 16:8 h L:D photoperiod). Means with the same lower case letter do not differ by Fisher's LSD test (P> 0.05). (F = 1.09; df = 6; P = 0.3897).
Fig. 1 in Regional susceptibilities of Rhopalosiphum padi (Hemiptera: Aphididae) to ten insecticides
Fig. 1. SaMpliNG reGioNs of Rhopalosiphum padi iN ChiNa. The reGioNs iNcluded BaicheNG of JiliN ProviNce (the populatioN code was NaMed as JLB), BaodiNG of Hebei ProviNce (HEB), LaNzhou of GaNsu ProviNce (GSL), TaiGu of ShaNxi ProviNce (SXT), Zibo of ShaNGdoNG ProviNce (SDZ), TaiaN of ShaNGdoNG ProviNce (SDT), XiaNyaNG of Shaaxi ProviNce (SAX), NaNyaNG of HeNaN ProviNce (HNN), Chuzhou of ANhui ProviNce (AHC), WuhaN of Hubei ProviNce (HBW), Beibei of ChoNGqiNG ProviNce (CQB), aNd GuiyaNG of Guizhou ProviNce (GZG).
Fig. 2 in Sublethal effects of indoxacarb and beta-cypermethrin on Rhopalosiphum padi (Hemiptera: Aphididae) under laboratory conditions
Fig. 2. Effects of beta-cypermethrin and indoxacarb sub-lethal concentrations on age-specific survival rate and age-specific fecundity of Rhopalosiphum padi F1 generation. CK: control treatment; B-LC10: LC10 of beta-cypermethrin; BLC30: LC30 of beta-cypermethrin; I-LC10: LC10 of indoxacarb; I-LC30: LC30 of indoxacarb.
Fig. 1 in Sublethal effects of indoxacarb and beta-cypermethrin on Rhopalosiphum padi (Hemiptera: Aphididae) under laboratory conditions
Fig. 1. Comparisons of development times of nymphs (mean ± SE) across all treatments (different letters indicate significant differences between populations at the P <0.05 level). CK: control treatment; B-LC10: LC10 of beta-cypermethrin; B-LC30: LC30 of beta-cypermethrin; I-LC10: LC10 of indoxacarb; I-LC30: LC30 of indoxacarb.
Fig. 1 in Characterization of Bacillus thuringiensis (Bacillaceae) strains pathogenic to Myzus persicae (Hemiptera: Aphididae)
Fig. 1. Protein profiles of the strains virulent to Myzus persicae. Lane 1: GP640, Lane 2: GP399, Lane 3: GP238, Lane 4: GP322, Lane 5: GP139, Lane 6: GP762, Lane 7: GP339, Lane 8: GP300, Lane 9: HD1, Lane 10: GP402, Lane 11: GP382, Lane 12: GP528, Lane 13: GP782, Lane 14: GP209, Lane 15: GP777, Lane 16: GP778, Lane 17: GP60, Lane 18: GP780.
Fig. 2. Type II in Effect of temperature on functional response of Aphidius gifuensis (Hymenoptera: Braconidae) parasitizing Myzus persicae (Hemiptera: Aphididae)
Fig. 2. Type II functional response curves fitted by Roger's random parasitoid equation (RRPE) of Aphidius gifuensis against Myzus persicae at various temperatures.
Fig. 1. Type II in Effect of temperature on functional response of Aphidius gifuensis (Hymenoptera: Braconidae) parasitizing Myzus persicae (Hemiptera: Aphididae)
Fig. 1. Type II functional response curves fitted by Holling's disc equation (HDE) of Aphidius gifuensis against Myzus persicae at various temperatures.
Fig. 5 in First Record of Lachnus chosoni (Hemiptera: Aphididae: Lachninae) in the Republic of Korea with Description of Sexual Morphs
Fig. 5. Male of Lachnus chosoni characters: (a) antenna; (b) small, rounded, protuberant secondary rhinaria on ANT III; (c) secondary rhinaria on ANT IV; (d) ANT V with primary rhinarium (arrow) and secondary rhinaria; (e) ultimate rostral segments; (f) hind tibiae chaetotaxy; (g) genitalia-bp-basal part of phallus, p-parameres, c-cauda.
Fig. 4 in First Record of Lachnus chosoni (Hemiptera: Aphididae: Lachninae) in the Republic of Korea with Description of Sexual Morphs
Fig. 4. Oviparous females of Lachnus chosoni characters: (a) hind tibiae with different length of inner (longer) and outer (shorter) setae and pseudosensoria area (arrows); (b) poorly visible, low mesosternal processes (arrows); (c) different types of pseudosensoria on hind tibiae-single, rounded (arrow), 8-shaped (dotted arrow) and double, oval (arrowhead); (d) egg capsules inside the abdomen; (e) genital plate with a median suture; (f) egg.
Fig. 2 in First Record of Lachnus chosoni (Hemiptera: Aphididae: Lachninae) in the Republic of Korea with Description of Sexual Morphs
Fig. 2. Representatives of Lachnus chosoni in life: (a) spring colony of apterous viviparous females and nymphs feeding on scars of a branch, (b) apterous viviparous females on leaves, (c) freshly moulted male with uniformly light brown legs, (d) autumnal colony of oviparous females and males visited by ants, (e) oviparous female and male in copula (in the bottom left corner magnification of the male genitalia and female perianal area), (f) oviparous females with freshly laid eggs.
Fig. 3 in First Record of Lachnus chosoni (Hemiptera: Aphididae: Lachninae) in the Republic of Korea with Description of Sexual Morphs
Fig. 3. Sexual morphs of Lachnus chosoni in mounted specimens: (a) oviparous female, (b) apterous male.
Fig. 1 in First Record of Lachnus chosoni (Hemiptera: Aphididae: Lachninae) in the Republic of Korea with Description of Sexual Morphs
Fig. 1. Known distribution of Lachnus chosoni in the Korean Peninsula: the type locality in North Korea (red circle), first records in South Korea (violet rhombus).
Fig. 1 in A comprehensive checklist and host plants of Aphididae (Aphidomorpha: Hemiptera) from Pakistan
Fig. 1. Species diversity in the different provinces/states of Pakistan. The number represents the known species in each province/territory in Pakistan.
Figure 2 in Orientation of Hippodamia variegata (Coleoptera: Coccinellidae) to healthy and Beauveria bassiana-infected Aphis fabae (Hemiptera: Aphididae) in an olfactometer system
Figure 2. Response of Hippodamia variegata to broad bean plants infested by A. fabae infected by Beauveria bassiana at the interval of 0 h after infection versus broad bean plants infested by A. fabae infected by B. bassiana at intervals of 24 (a), 48 (b), and 72 (c) h after infection. The white bars indicate the numbers of insects choosing broad bean plants infested by A. fabae infected by B. bassiana at intervals of 24, 48, and 72 h after infection, whereas the black bars indicate the numbers of insects that chose broad bean plants infested by A. fabae infected by B. bassiana at the interval of 0 h after infection.
Figure 4 in Orientation of Hippodamia variegata (Coleoptera: Coccinellidae) to healthy and Beauveria bassiana-infected Aphis fabae (Hemiptera: Aphididae) in an olfactometer system
Figure 4. Response of Hippodamia variegata to broad bean plants infested by A. fabae infected by Beauveria bassiana at the interval of 48 h after infection versus broad bean plants infested by A. fabae infected by B. bassiana at the interval of 72 h after infection. The white bars indicate the numbers of insects choosing broad bean plants infested by A. fabae infected by B. bassiana at the interval of 72 h after infection, whereas the black bars indicate the numbers of insects that chose broad bean plants infested by A. fabae infected by B. bassiana at the interval of 48 h after infection.
Figure 3. The 50 in Is the subfamily Eriosomatinae (Hemiptera: Aphididae) monophyletic?
Figure 3. The 50% majority-rule consensus tree from the ML analysis combining sequences from 2 mitochondrial genes (COI and COII) and 2 nuclear genes (EF-1α and LWO). Nodal support values were omitted. Note the comb-like topology.
Figure 1 in Is the subfamily Eriosomatinae (Hemiptera: Aphididae) monophyletic?
Figure 1. Previous phylogenetic hypotheses for the Eriosomatinae: a) Zhang and Chen (1999), based on morphology; b) Moran and von Dohlen (2000), based on 12S, partial topology, 8 sampled species; c) Ortiz-Rivas et al. (2010), based on LWO combined with other genes, partial topology, 10 sampled species; d) Zhang and Qiao (2008), based on EF-1α, 25 sampled species, but only 2 species in Eriosomatini.
Figure 4 in Is the subfamily Eriosomatinae (Hemiptera: Aphididae) monophyletic?
Figure 4. The Bayesian tree of Eriosomatinae combining sequences from 2 mitochondrial genes (COI and COII) and 2 nuclear genes (EF-1α and LWO). Nodes in Table 3 are marked as P = Pemphigini, E = Eriosomatini, F = Fordini, M = Melaphidina, and O = out-group. Nodal supports from different algorithms are listed in the order BI/ML/MP; the sample IDs are presented after the species names.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.