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27 results for “Feltia”
Fig. 4 in Asilidae (Diptera: Brachycera) - natural hosts of Steinernema feltiae (Rhabditida: Steinernematidae) at the Zemen Gorge region
Fig. 4. Caudal view of the male S. feltiae Fig. 3. Head capsule of the host larva. Scale isolated from the host. Scale bar: 25 bar: 0.3 mm. µm.
Fig.1 in Asilidae (Diptera: Brachycera) - natural hosts of Steinernema feltiae (Rhabditida: Steinernematidae) at the Zemen Gorge region
Fig.1. Fragment of the investigated habitat Fig.2. Nematodes emerging from the asilid with Aegopodium podagraria. host larva. Scale bar: 1 mm.
Fig. 1 in Development of Steinernema feltiae (Rhabditida: Steinernematidae) in larvae of Chaetonyx robustus (Coleoptera: Orphnidae)
Fig. 1. Imago and larvae of Chaetonyx robustus, collected in soil of the investigated habitat (22.04.2011, D. Gradinarov leg.). Scale bar: 10 mm.
Fig. 3. First parasitic generation emerging Fig. 4. Juveniles migration from a in Development of Steinernema feltiae (Rhabditida: Steinernematidae) in larvae of Chaetonyx robustus (Coleoptera: Orphnidae)
Fig. 3. First parasitic generation emerging Fig. 4. Juveniles migration from a host. from host. Scale bar: 1 mm. Scale bar: 1 mm.
Fig. 2 in Management of flower thrips in Florida strawberries with Steinernema feltiae (Rhabditida: Steinernematidae) and the insecticide sulfoxaflor
Fig. 2. Least square means (± 95% confidence intervals) for (A) adult and (B) larval thrips (Frankliniella bispinosa) per 10 strawberry flowers from research plots near Balm, Florida, sprayed 3, 7, and 16 Mar 2016 with Steinernema feltiae and 3 and 16 Mar 2016 with insecticides. Treatments were applied and reapplied when total thrips counts exceeded 5 per flower. Means in lower panel with the same letter are not significantly different (Tukey's HSD test, α = 0.05) (Experiment 2).
Fig. 1 in Management of flower thrips in Florida strawberries with Steinernema feltiae (Rhabditida: Steinernematidae) and the insecticide sulfoxaflor
Fig. 1. Least square means (± 95% confidence intervals) for (A) adult and (B) larval thrips (Frankliniella bispinosa) per 10 strawberry flowers from research plots near Balm, Florida, sprayed 26 Feb, and 1, 5, and 9 Mar 2016 with Steinernema feltiae or insecticides. Means in each panel with the same letter are not significantly different (Tukey's HSD test, α = 0.05) (Experiment 1).
Fig. 3 in Management of flower thrips in Florida strawberries with Steinernema feltiae (Rhabditida: Steinernematidae) and the insecticide sulfoxaflor
Fig. 3. Hourly temperature (lef y-axis), rainfall, and relative humidity (right y-axis) 26 Feb to 25 Mar 2016 at Balm, Florida.
Fig. 2 in Development of Steinernema feltiae (Rhabditida: Steinernematidae) in larvae of Chaetonyx robustus (Coleoptera: Orphnidae)
Fig. 2. Liva (A) and infected larva (B) of Chaetonyx robustus. Scale bar: 2 mm.
FIGURE 3 in Revalidation and redescription of Feltia deprivata (Walker) (= bilitura of authors) (Lepidoptera: Noctuidae), a pest species on South America
FIGURE 3. Pseudoleucania bilitura Holotype, male (Muséum National d'Histoire Naturelle, Paris, inventory number: MNHN EL n° 2016). Scale bars = 10 mm.
FIGURES 12–13 in Revalidation and redescription of Feltia deprivata (Walker) (= bilitura of authors) (Lepidoptera: Noctuidae), a pest species on South America
FIGURES 12–13. Distribution map of F. derivata. 12, distribution. 13, enlargement of squared area on 11. Black dots = data from material revised, red dots = data from bibliographical resources.
FIGURES 1–2 in Revalidation and redescription of Feltia deprivata (Walker) (= bilitura of authors) (Lepidoptera: Noctuidae), a pest species on South America
FIGURES 1–2. Feltia deprivata variation of color pattern in adults. 1, male. 2, female. Scale bars = 10 mm.
FIGURES 4–11 in Revalidation and redescription of Feltia deprivata (Walker) (= bilitura of authors) (Lepidoptera: Noctuidae), a pest species on South America
FIGURES 4–11. Genital morphology of F. deprivata. 4, male genitalia (ventral view, aedeagus omitted). 5, male genitalia (lateral view, aedeagus omitted). 6, median area of male genitalia (ventral view, vinculum and tegumen omitted), with detail on transtilla. 7, juxta (ventral view). 8, aedeagus (lateral view). 9, aedeagus (dorsal view). 10, female genitalia (lateral view). 11, female genitalia (dorsal view).
FIGURE 6. Phylogenetic relationships between 23 in Morphological and molecular characterization of a new isolate of Steinernema feltiae (Filipjev, 1934) from Vancouver, Canada, with morphometrical comparison with the topotype population from Russia
FIGURE 6. Phylogenetic relationships between 23 species and strains of Steinernema with bootstrap analysis of ITS regions. The eight strains of S. feltiae from a monophyletic group. Numbers at the nodes represent bootstrap proportion.
FIGURE 5 in Morphological and molecular characterization of a new isolate of Steinernema feltiae (Filipjev, 1934) from Vancouver, Canada, with morphometrical comparison with the topotype population from Russia
FIGURE 5. SEM of infective juvenile of S. feltiae strain BC showing lateral field pattern. A, anterior region showing smooth head, amphid, and one line in lateral field. B, lateral field with two ridges. C, lateral field with two ridges anteriorly, seven ridges posteriorly. D, lateral field with eight ridges. E, lateral field in posterior region showing four ridges near anus. F, lateral field with two ridges and phasmid. Scale bars: A=4.29 µm, B=5.0 µm, C=7.5 µm, D=7.5 µm, E=23.1 µm, F=1.67 µm.
FIGURE 4 in Morphological and molecular characterization of a new isolate of Steinernema feltiae (Filipjev, 1934) from Vancouver, Canada, with morphometrical comparison with the topotype population from Russia
FIGURE 4. Light microscope photographs of S. feltiae strain BC. A–C, infective juvenile showing excretory pore, basal bulb and long tail. D–F, second generation female, D, tail, E, young, F, old specimen. Scale bars: A–C=14 µm, D=32 µm, E, F=20 µm.
FIGURE 3 in Morphological and molecular characterization of a new isolate of Steinernema feltiae (Filipjev, 1934) from Vancouver, Canada, with morphometrical comparison with the topotype population from Russia
FIGURE 3. SEM of female of S. feltiae strain BC. A, an abnormal face view. B, a normal face view. C, vulva. D–E, variations of female tail tip. Scale bars: A=6.67 µm, B=10.0 µm, C=15 µm, D=12 µm, E=15 µm, F=16.7 µm.
FIGURE 2 in Morphological and molecular characterization of a new isolate of Steinernema feltiae (Filipjev, 1934) from Vancouver, Canada, with morphometrical comparison with the topotype population from Russia
FIGURE 2. SEM and light microscopy. Comparative morphology of spicules S. feltiae and S. oregonense. A, spicule of S. feltiae strain SN. B, spicule of S. oregonense. C,D, variation of spicule of S. feltiae strain BC. Scale bars: A=21 µm, B=24 µm, C=24 µm, D=16 µm (in C).
FIGURE 1 in Morphological and molecular characterization of a new isolate of Steinernema feltiae (Filipjev, 1934) from Vancouver, Canada, with morphometrical comparison with the topotype population from Russia
FIGURE 1. SEM of male of S. feltiae strain BC. A, face view. B, C, posterior regions with prominent genital papillae in B and not very prominent in C. D–F, variation of mucron and tail tip. Scale bars: A=7.5 µm, B=50.0 µm, C=85.7 µm, D=23.1 µm, E=10 µm, F=8.57 µm.
FIGURE 8 in Morphological and molecular profiling of an entomopathogenic nematode Steinernema feltiae: Unlocking its biocontrol potential against vegetable insect pests
FIGURE 8. Median lethal time (LT50) of Steinernema feltiae in the larvae of different insect pests at different time intervals and at different nematode concentrations, respectively.
FIGURE 6 in Morphological and molecular profiling of an entomopathogenic nematode Steinernema feltiae: Unlocking its biocontrol potential against vegetable insect pests
FIGURE 6. Maximum-likelihood phylogenetic tree between Steinernema feltiae and other species of Steinernema in the Feltiae-group based on nucleotide sequences of the D2–D3 expansion segments of large subunit (28S) of rRNA flanked by primers D2F and 536. Numbers at nodes represent bootstrap values based on 100 replications. Bars represent average nucleotide substitutions per sequence position. NCBI accession numbers of the nucleotide sequences used for the analyses are shown next to the species names. The scale bar shows the number of substitutions per site.
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