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369 results for “insecticides”
Figure 1 in Capturing Males of Pestiferous Fruit Flies (Diptera: Tephritidae): Is the Combination of Triple-Lure Wafers and Insecticidal Strips as Effective as Standard Treatments?
Figure 1. Captures of Ceratitis capitata, Bactrocera dorsalis, and Bactrocera cucurbitae males in Jackson traps baited with standard lures or triple-lure wafers over a 12-week interval in October-December, 2013, in a coffee field near Haleiwa, Oahu. Symbols represent mean values of 15 traps; error bars represent 1 SE.
Fig. 2 in Insecticidal activity of three plant extracts against adult Ips typograpgus L. under laboratory conditions
Fig. 2. Concentration–mortality response curves from the probit analyses testing insecticide effects of plant extracts against adults ofIps typographus in laboratory bioassays.
Fig. 1 in Insecticidal activity of three plant extracts against adult Ips typograpgus L. under laboratory conditions
Fig. 1. Mean cumulative mortality* of Ips typographus adults four days after treatments with different concentrations of three plant extracts in laboratory bioassays. The error bars represent the standard errors of means. (*corrected for a natural mortality in the control)
Fig. 3 in Insecticidal activity of three plant extracts against adult Ips typograpgus L. under laboratory conditions
Fig. 3. Kaplan-Meier estimates of the survival curves for Ips typographus adults treated with the plant extracts (2.5%) in laboratory bioassays.
Figure 1. A in Effects of the pyrethroid insecticide deltamethrin on the hemocytes of Galleria mellonella
Figure 1. A- Prohemocyte, B- plasmatocyte, C- spherulocyte, D- oenocyte, and E- granulocyte in the last instar of G. mellonella.
Figure 1 in Toxicity of insecticides to the egg parasitoids Telenomus podisi and Trissolcus teretis (Hymenoptera: Scelionidae)
Figure 1 Bioassay setup. Potter Spray Tower (A), experimental cage (B), Duran tube with adult parasitoids inside covered with aluminum foil used to introduce the wasps into the experimental cage (C), glass plate being sprayed with the Potter Spray Tower before the setup of the experimental cage (D), adult cages mounted with the Duran tube connected (E), experimental cages setup with circulating air flow allowing the elimination of possible toxic gases (F).
Fig. 3 in Contrasting patterns of insecticide resistance and knockdown resistance (kdr) in Aedes aegypti populations from Jacarezinho (Brazil) after a Dengue Outbreak
Fig. 3. Allelic frequencies of 1016Val and 1016Ile in the Nav of A.aegypti populations from Jacarezinho in 2011 and 2012. Besides, the allelic frequencies of the Val1016Ile mutation by regions (Region I–IV) for 2012 are presented.
Fig. 2 in Contrasting patterns of insecticide resistance and knockdown resistance (kdr) in Aedes aegypti populations from Jacarezinho (Brazil) after a Dengue Outbreak
Fig. 2. Jacarezinho map shows the collection sites by regions in the urban area used for the analysis of the Val1016Ile mutation in 2012. Additionally, the main roads that cross Jacarezinho are presented.
Figure 3 in Lichens in the nests of European starling Sturnus vulgaris serve a mate attraction rather than insecticidal function
Figure 3. Number of events in which lichens were added to starling nests during the nesting cycle. Before: period before the start of nest building. Beginning: the first day of nest building. Middle: between the second and the last day of the nest building. After: after the starlings had complete nest building.
Figure 2 in Lichens in the nests of European starling Sturnus vulgaris serve a mate attraction rather than insecticidal function
Figure 2. Nest box with the lichen Ramalina celastri that was used by some of the starlings at the beginning of nest building.
Figure 1 in Lichens in the nests of European starling Sturnus vulgaris serve a mate attraction rather than insecticidal function
Figure 1. Spatial location of the nests in the study area. Full circles: nests with lichens, empty triangles: nests without lichens, empty circles: the 25% of nests without lichens that started the egg-laying earlier, full triangles: the 25% of nests with lichens that started the egg-laying earlier.
Figure 3 in Insecticidal effect of diatomaceous earth and dolomite powder against Corn weevil Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae)
Figure 3. Pictures of Sitophilus zeamais control taken by scanning electron microscopy (SEM). A. Dorsal view: trichoid sensilla (Se), sensilla (S), antenna (A), rostrum (R), elytrum (E). Bar = 500 µm. B. Rostrum and antenna: trichoid sensilla (Se), sensilla (S). Bar = 100 µm. C. Antenna: trichoid sensilla (Se). Bar = 20 µm. D. Elytrum: sensilla (S), suture (Su). Bar = 20 µm. E. Elytrum: sensilla (S), suture (Su). Bar = 50 µm. F. Abdomen, ventral view: sensilla (S). Bar = 10 µm.
Figure 2 in Insecticidal effect of diatomaceous earth and dolomite powder against Corn weevil Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae)
Figure 2. Mortality at different concentrations (mg) of diatomaceous earth and dolomite powder used for control of Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae), after different exposure times. DE:Diatomaceous earth and DOL: Dolomite powder.
Figure 5 in Insecticidal effect of diatomaceous earth and dolomite powder against Corn weevil Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae)
Figure 5. Pictures of Sitophilus zeamais exposed to inert dusts taken by scanning electron microscopy (SEM). A. Elytrum (E) of insect exposed to diatomaceous earth: sensilla (S), suture (Su). Bar = 200 µm. B. Elytrum (E) of insect exposed to dolomite powder: sensilla (S), suture (Su). Barra = 20 µm. C. Leg of insect exposed to dolomite powder: sensilla (S). Bar = 100 µm. D. Claw of insect exposed to dolomite powder. Bar = 50 µm.
Figure 5 in First report on mild insecticide resistance in newly established Aegean Aedes albopictus populations of Turkey
Figure 5. Mortality rates against fenitrothion in Aedes albopictus populations of the Aegean region (Mean ± S.E. Same lower case letters above error bars indicates nonsignificant difference at p> 0.05 based on the ANOVA results followed by Tukey's HSD test).
Figure 6 in First report on mild insecticide resistance in newly established Aegean Aedes albopictus populations of Turkey
Figure 6. Mortality rates against permethrin in Aedes albopictus populations of the Aegean region (Mean ± S.E. Same lower case letters above error bars indicates nonsignificant difference at p> 0.05 based on the ANOVA results followed by Tukey's HSD test).
Figure 4 in First report on mild insecticide resistance in newly established Aegean Aedes albopictus populations of Turkey
Figure 4. Mortality rates against bendiocarb in Aedes albopictus populations of the Aegean region (Mean ± S.E. Same lower case letters above error bars indicates nonsignificant difference at p> 0.05 based on the ANOVA results followed by Tukey's HSD test).
Figure 3 in First report on mild insecticide resistance in newly established Aegean Aedes albopictus populations of Turkey
Figure 3. Mortality rates against propoxur in Aedes albopictus populations of the Aegean region (Mean ± S.E. Same lower case letters above error bars indicates nonsignificant difference at p> 0.05 based on the ANOVA results followed by Tukey's HSD test).
Figure 2 in First report on mild insecticide resistance in newly established Aegean Aedes albopictus populations of Turkey
Figure 2. Mortality rates against DDT in Aedes albopictus populations of the Aegean region (Mean ± S.E. Same lower case letters above error bars indicates nonsignificant difference at p> 0.05 based on the ANOVA results followed by Tukey's HSD test).
Fig. 3 in Toxicity for control of Frankliniella schultzei and Selenothrips rubrocinctus (Thysanoptera: Thripidae) of several common synthetic insecticides
Fig. 3. The bioassays to evaluate the toxicity of selected insecticides on common blossom thrips, Frankliniella schultzei, and red-banded thrips, Selenothrips rubrocinctus, were conducted in 90 mL plastic cups. Each cup had 10 thrips and a 3 cm long piece of insecticide-treated bean.
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