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36,014 results for “diptera”
Figs 14-18 in Three new species of the genus Ommatius Wiedemann from Hainan,China (Diptera: Asilidae)
Figs 14-18. Ommatius jianfenglingensis sp. nov., male genitalia. 14–15. Epandrium and cercus, dorsal and lateral views. 16–17. Hypandrium and gonocoxites, ventral and lateral views. 18. Aedeagus, dorsal view. Scale bars = 0.1 mm.
Figs 7–13 in Three new species of the genus Ommatius Wiedemann from Hainan,China (Diptera: Asilidae)
Figs 7–13. Ommatius huoae sp. nov., male genitalia. 7–8. Epandrium and cercus, dorsal and lateral views. 9–10. Hypandrium and gonocoxites, ventral and lateral views. 11–13. Aedeagus, ventral, dorsal and lateral views. Scale bars = 0.1 mm.
Figs 1–6 in Three new species of the genus Ommatius Wiedemann from Hainan,China (Diptera: Asilidae)
Figs 1–6. Ommatius corolla sp. nov., male genitalia. 1–2. Epandrium and cercus, dorsal and lateral views. 3–4. Hypandrium and gonocoxites, ventral and lateral views. 5–6. Aedeagus, lateral and dorsal views. Scale bars = 0.1 mm.
Fig. 2 in A new live trap for the acoustically orienting parasitoid fly Emblemasoma erro (Diptera: Sarcophagidae)
Fig. 2. Details of trap construction showing a) the trap box and b) the speaker box. To reveal internal components, the front-facing, side plywood panels of the trap and speaker boxes are not illustrated. Also, for clarity, only 3 of the 5 wire screen cones of the trap box are illustrated.
Fig. 1 in A new live trap for the acoustically orienting parasitoid fly Emblemasoma erro (Diptera: Sarcophagidae)
Fig. 1. The complete live trap deployed in the field. Captured flies are visible in the holding jar assembly at the top of the trap box.
Fig. 6 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 6. Four examples of the tissue expression profiling of unknown distinct unigenes (>500 bp) expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Relative expression levels were determined as described in Fig. 5.
Fig. 4 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 4. Kyoto encyclopedia of gene and genomes (KEGG) analysis of unigenes expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Each category contains more than 1 unigene sequences.
Fig. 2 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 2. Clusters of orthologous groups (COG) functional classification of unigenes expressed highly and specifically in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis.
Fig. 1 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 1. Statistics of sequences expressed specifically in each analyzed tissue of Bactrocera dorsalis.
Fig. 5 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 5. Six examples of the tissue expression profiling of predicted distinct unigenes (>500 bp) expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Relative expression levels were determined by qRT-PCR in head (HE), thorax (TH), abdomen (AB), midgut (MG), fat body (FB), Malpighian tubules (MT), testes (TE), and male accessory glands and ejaculatory duct (MAG) samples from B. dorsalis males. Relative expression levels were calculated based on the value in head, which was ascribed an arbitrary value of 1. Different letters above the bars indicate significant differences based on Tukey's test (P ≤ 0.05).
Fig. 3 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct
Fig. 3. Gene ontology (GO) classification of unigenes expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis.
Fig. 1 in Evaluation of food lures for fruit flies (Diptera: Tephritidae) captured in a citrus orchard of the Serra Gaúcha
Fig. 1. Mean number of adult Anastrepha fraterculus (male and female) flies captured per trap per day (FTD) with McPhail monitoring traps containing food lures in a citrus orchard growing the Citrus sinensis cv. 'Valência' from Nov 2012 to Oct 2013. Municipality of Pinto Bandeira, Rio Grande do Sul State, Brazil. The continuous horizontal line indicates an FTD index of 0.5 (economic injury level).
Fig. 1 in Mixing male lures results in an effective multispecies bait for trapping Bactrocera (Diptera: Tephritidae) fruit flies
Fig. 1. Numbers of Bactrocera dorsalis male flies captured in traps baited with methyl eugenol (ME) alone or a mixture of ME and raspberry ketone (RK, a natural analogue of cue lure). Comparisons involved 3 mixtures in ME:RK ratios (wt:wt) of 95:5, 90:10, and 85:15. Symbols represent means (± SE) of 15 traps per lure type at 2 wk intervals over an 8 wk sampling period.
Fig. 2 in Determination of instars of Bactrocera dorsalis (Diptera: Tephritidae)
Fig. 2. Frequency histograms and scatter plots of measurements of 5 morphological variables for Bactrocera dorsalis larvae.
Fig. 3 in Determination of instars of Bactrocera dorsalis (Diptera: Tephritidae)
Fig. 3. Morphological characteristics of the pharyngeal sclerite, mouth hooks, anterior spiracles, and posterior spiracles of Bactrocera dorsalis larvae in three instars. A, C, E: Pharyngeal sclerite and mouth hook of the 1st, 2nd, and 3rd instar, respectively; B, D, F: posterior spiracles of the 1st, 2nd, and 3rd instar, respectively; red arrows indicate the anterior spiracles of the 2nd and 3rd instar in C and E, respectively.
Fig. 1 in Determination of instars of Bactrocera dorsalis (Diptera: Tephritidae)
Fig. 1. Schematic diagram of the measurements for Bactrocera dorsalis larvae. A: Body length of B. dorsalis larvae (L); B: pharyngeal sclerite length (X) and width (Y); C: mouth hook length (Z) and width (K).
Fig. 3 in Novel aspects of Drosophila suzukii (Diptera: Drosophilidae) biology and an improved method for culturing this invasive species with a modified D. melanogaster diet
Fig. 3. Effect of triethylamine anesthetic exposure on the recovery of Drosophila adults: D. melanogaster (white circles, n = 181 adults), D. suzukii (black circles, n = 175 adults).
Fig. 2 in Novel aspects of Drosophila suzukii (Diptera: Drosophilidae) biology and an improved method for culturing this invasive species with a modified D. melanogaster diet
Fig. 2. Effects of dietary ethanol (normal environmental ethanol range ≈ 0– 9% ethanol) on Drosophila suzukii survival when compared with D. melanogaster tolerance to ethanol (top graph) and sex-specific sensitivities of D. suzukii adults to ethanol (bottom graph). Summary of probit analyses are provided and statistics with bo = intercept estimate, b1 = estimated slope estimate for each fly species, with b1 = 0 for the baseline control in each graph (D. suzukii [top graph], D. suzukii males [bottom graph]).
Fig. 1 in Novel aspects of Drosophila suzukii (Diptera: Drosophilidae) biology and an improved method for culturing this invasive species with a modified D. melanogaster diet
Fig. 1. Dietary manipulation of Drosophila suzukii cultures based on the use of 5 berry species (blackberry, strawberry, black cherry, blueberry, and grape) with a no-fruit (No Fruit) control (grey bars), and cultures to which yeast was added (+Y) or omitted (−Y) from 4-24® drosophila media (white bars). Asterisks indicate mean differences from 2 respective baseline controls (B), i.e., Blackberry−Y (14 d) and Blackberry+Y (21 d), according to multiple Wilcoxon 2-sample tests.
Fig. 1 in Bacillus thuringiensis subspecies kurstaki reduces competition by Parapoynx diminutalis (Lepidoptera: Crambidae) in colonies of the hydrilla biological control agent Cricotopus lebetis (Diptera: Chironomidae)
Fig. 1. Emergence of Parapoynx diminutalis adults from Bacillus thuringiensis (subspecies kurstaki; Btk) treated water containing Hydrilla verticillata. Moth emergence is shown as a proportion of initial larvae. Bars are means ± SE. Asterisks indicate significance between concentrations of Btk per 3.8 L of well water and the control using Dunnett's test.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.