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107 results for “Bactrocera dorsalis”
Fig. 1 in Identification and characterization of three juvenile hormone genes from Bactrocera dorsalis (Diptera: Tephritidae)
Fig. 1. Multiple sequence alignment and phylogenetic analysis of JHEHs from Bactrocera dorsalis and other insects. (A) Sequence alignment. The sequences of B. dorsalis JHEHs are compared with JHEH from Drosophila melanogaster (Dm), Bombyx mori (Bm), Manduca sexta (Ms), and Apis mellifera (Am). The catalytic triad (Asp232, Glu409, and His436), 2 tyrosine residues (Tyr 304 and Tyr380), and HGXP motif are labeled with asterisks. The HGXP motif is underlined. (B) Phylogenetic analysis of JHEH homologs. The tree was generated with MEGA 5 using the neighbor-joining method. Nodes with>50% bootstrap values (1,000 replicates) are indicated on branches. GenBank accession numbers of all sequences are listed in the tree.
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. 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. 2 in Attraction of Bactrocera cucurbitae and Bactrocera dorsalis (Diptera: Tephritidae) to beer waste and other protein sources laced with ammonium acetate
Fig. 2. Response of males of Bactrocera cucurbitae and B. dorsalis to GF-120® NF Naturalyte® Fruit Fly Bait (= GF-120), Bugs for Bugs® Fruit Fly Bait (= Bugs for Bugs), Buminal® (= Buminal), and water (negative control) either in the absence (A), or presence (B) of ammonium acetate (= AA). For each species, different letters (lowercase: B. cucurbitae; uppercase: B. dorsalis) indicate significant differences according to ANOVA and the Fisher LSD tests at P ≤ 0.05.
Fig. 3 in Attraction of Bactrocera cucurbitae and Bactrocera dorsalis (Diptera: Tephritidae) to beer waste and other protein sources laced with ammonium acetate
Fig. 3. Response of females of Bactrocera cucurbitae and B. dorsalis to GF- 120® NF Naturalyte® Fruit Fly Bait (= GF-120), Bugs for Bugs® Fruit Fly Bait (= Bugs for Bugs), Buminal® (= Buminal), and water (negative control) either in the absence (A), or presence (B) of ammonium acetate (= AA). For each species, different letters (lowercase: B. cucurbitae; uppercase: B. dorsalis) indicate significant differences according to ANOVA and the Fisher LSD tests at P ≤ 0.05.
Fig. 1 in Attraction of Bactrocera cucurbitae and Bactrocera dorsalis (Diptera: Tephritidae) to beer waste and other protein sources laced with ammonium acetate
Fig. 1. Response of adult males (A) and females (B) of Bactrocera cucurbitae and B. dorsalis in field cages to Nu-Lure® Insect Bait (= Nu-Lure), beer waste, Bugs for Bugs® Fruit Fly Bait (= Bugs for Bugs), and Buminal® (= Buminal) either alone or with added ammonium acetate (= AA) or ammonium carbonate (= AC). Water was used as a negative control. For each fly species and sex, different letters (lowercase: B. cucurbitae; uppercase: B. dorsalis) indicate significant differences according to ANOVA and the Fisher LSD tests at P ≤ 0.05.
Fig. 4 in Attraction of Bactrocera cucurbitae and Bactrocera dorsalis (Diptera: Tephritidae) to beer waste and other protein sources laced with ammonium acetate
Fig. 4. Response of males of Bactrocera cucurbitae and B. dorsalis to GF-120® NF Naturalyte® Fruit Fly Bait (= GF-120), beer waste, Nu-Lure® Insect Bait (= Nu-Lure), and water (negative control) either in the absence (A), or presence (B) of ammonium acetate (= AA). For each species, different letters (lowercase: B. cucurbitae; uppercase: B. dorsalis) indicate significant differences according to ANOVA and the Fisher LSD tests at P ≤ 0.05.
Figure 3 in First Record of Bactrocera (Bactrocera) dorsalis (Hendel, 1912) (Diptera: Tephritidae) on Hedychium coronarium (family Zingiberaceae) from India
Figure 3. Bactrocera (Bactrocera) dorsalis (Hendel, 1912) visiting the whgite flower of Hedychium coronarium.
Figure 1 in First Record of Bactrocera (Bactrocera) dorsalis (Hendel, 1912) (Diptera: Tephritidae) on Hedychium coronarium (family Zingiberaceae) from India
Figure 1. Map showing location of the study area (Garden and agricultural landscape, Block B, Bangur Avenue, North Kolkata).
Fig. 1 in Using hydrogen stable isotope ratios to trace the geographic origin of the population of Bactrocera dorsalis (Diptera: Tephritidae) trapped in northern China
Fig. 1. Implied relationship standard curve equation between Bactrocera dorsalis and precipitation based on a δ2H stable isotope (solid line indicates the linear regression and dash lines indicate the 95% confident intervals).
Fig. 2 in Use of ITS-1 to identify Bactrocera dorsalis and Bactrocera occipitalis (Diptera: Tephritidae): a case study using flies trapped in California from 2008 to 2018
Fig. 2. ML tree (log likelihood –1370.3141) of elongation factor 1‑alpha (EF1α) gene based on Jukes‑Cantor model. The California fly (16V457) with Bactrocera occipitalis ITS‑1 sequence is marked with an open circle dot. Five flies trapped in California that have ITS‑1 sequences that match Bactrocera dorsalis and reported in Barr et al. (2014a) are marked with black dots.
Fig. 1 in Use of ITS-1 to identify Bactrocera dorsalis and Bactrocera occipitalis (Diptera: Tephritidae): a case study using flies trapped in California from 2008 to 2018
Fig. 1. ML tree (log likelihood –2782.3671) of C3p790 fragment of COI gene based on the Tamura model with Gamma distributed rates and Invariant sites (T92+G+I). The California fly (16V457) with Bactrocera occipitalis ITS‑1 sequence is marked with an open circle dot. Five flies trapped in California that have ITS‑1 sequences that match Bactrocera dorsalis and reported in Barr et al. (2014a) are marked with black dots. Operational Taxonomic Units and branches are collapsed for species in clades. The collapsed B. dorsalis clade includes both B. dorsalis and B. carambolae records.
Fig. 5 in Use of ITS-1 to identify Bactrocera dorsalis and Bactrocera occipitalis (Diptera: Tephritidae): a case study using flies trapped in California from 2008 to 2018
Fig. 5. Images of thoraces of the fly (16V457) with Bactrocera occipitalis ITS‑1 sequence and a Bactrocera dorsalis fly. Areas without microtrichia are highlighted in green in the smaller pictures.
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