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22 results for “acaricide”
Figure 4 in Acaricidal potential of Euphorbia seguieriana and E. helioscopia (Euphorbiaceae) extracts against Tetranychus urticae (Acari: Tetranychidae)
Figure 4. HPLC chromatograms of Euphorbia helioscopia (a) and E. seguieriana (b) methanol extracts used for measuring quercetin content (c) in both plant species (the data is based on only one replicate measurement).
Figure 3 in Acaricidal potential of Euphorbia seguieriana and E. helioscopia (Euphorbiaceae) extracts against Tetranychus urticae (Acari: Tetranychidae)
Figure 3. HPLC chromatograms of Euphorbia helioscopia (a) and E. seguieriana (b) methanol extracts used for
Figure 2 in Target-site insensitivity to some acaricides in a field population of Tetranychus urticae Koch (Acari: Tetranychidae) from Egypt
Figure 2. Multiple alignment of the amino acid sequences of T. urticae acetylcholinesterase (AChE) between Eg-Bernasht population and GenBank published populations. Tetranychus urticae AChE sequences were performed local as well as global alignments, using BLASTX search protein databases, using a translated nucleotide (NCBI). Three different specific primer sets (1, 2, and 3; Table 1) contained 422 amino acids of AChE gene. Dots: indicate amino acid similarity. Digital number: amino acid position on the AChE protein.
Figure 1 in Target-site insensitivity to some acaricides in a field population of Tetranychus urticae Koch (Acari: Tetranychidae) from Egypt
Figure 1. Products were imaged on a gel post electrophoresis. Tetranychus urticae acetylcholinesterase (AChE) gene fragment amplified expected sizes (639 bp, 571 bp, and 560 bp), using specific primers sets (1, 2, and 3, respectively). Tetranychus urticae voltage-gated sodium channel (VGSC) gene fragments were amplified products (226 bp, 225 bp, and 292 bp), using specific primers primer sets (4, 5, and 6, respectively). Tetranychus urticae glutamategated chloride channel (GluCl1, GluCl3) genes and chitin synthase 1 (CHS1) gene amplified products (263 bp, 251 bp, 541 bp), using primer sets (7, 8, and 9 respectively). EtBr was added to the gel before electrophoresis to a final concentration of 0.5 μg/ml, followed by separation at 100 V for 1 h. The gel was exposed to UV light and the picture was taken with a gel documentation system. Letter a: sample 1, letter b: sample 2, (-): no DNA templates. M:100 bp DNA ladder.
Fig. 7 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 7. Alignment of the predicted amino acid sequences of the CYP307A1 in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. We detected a sense amino acid mutation (14-threonine to serine).. This figure is shown in color in a supplementary document online as Suppl. Fig. 7 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 5 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 5. Alignment of the predicted amino acid sequences of CYP307A1 in Panonychus citribetween the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. Only one amino acid mutation (278-lysine to glutamine) was detected.. This figure is shown in color in a supplementary document online as Suppl. Fig. 5 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 6 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 6. Nucleotide sequence comparison of CYP381A2 in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. Just one SNP site was detected. The nucleotide transition of A to T was at position 40.. This figure is shown in color in a supplementary document online as Suppl. Fig. 6 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 4 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 4. Nucleotide sequence comparison of the CYP307A1 in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. Mazarine shading indicates identities and different color shading represents mutations. "-" represents no sequence to compare. Three SNP sites were detected in all. The first nucleotide mutation (A to C) is located at 841, the second mutation is 1395-T to C, and the final mutation is 1491-T to C.. This figure is shown in color in a supplementary document online as Suppl. Fig. 4 in Florida Entomologist 98(1) (March 2015) at http://purl.fcla.edu/fcla/entomologist/browse.
Fig. 3 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 3. Quantitative Real-time PCR analysis of CYPs in Panonychus citri between the hexythiazox-resistant (RR) and susceptible (SS) strains. The numbers of genes down-regulated and up-regulated in the RR relative to the SS are indicated above or below the X axis. The light or dark gray was susceptible strain and resistant strain, respectively.
Fig. 1 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 1. Number, family and clan distribution of cytochrome P450 genes in Panonychus citri. The number shown along each column represents the P450 family and the number in parenthesis is the number of individual genes in the corresponding family. The P450 gene sequence information generated is from the VectorBase of the P. citri transcriptome sequence.
Fig. 2 in Differential analysis of the cytochrome p450 acaricide-resistance genes in Panonychus citri (Trombidiformes: Tetranychidae) strains
Fig. 2. Neighbor-joining phylogenetic analysis of cytochrome P450 from Panonychus citri and Tetranychus urticae. 4clans were observed. There are species (P. citri and T. urticae) in the phylogenetic tree. Only 10 sequences belong to T. urticae; A (Pc) before the CYP name denotes P. citri, a (Tu) before the CYP name denotes T. urticae. Numbers at nodes are bootstrap values.
Fig. 4 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 4. LC50 values (± 95% confidence interval) for 7 AIs screened against a known-susceptible lab colony and 3 field-collected populations of Tetranychus urticae. When present, the dashed line indicates the amount of AI in the maximum labelled field rate. This value also is indicated in each graph by "FR=". The resistance ratio of each AI × population is written above each data point.
Fig. 1 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 1. Mean (± SE) spider mite (Tetranychus urticae) counts per tomato leaflet in a 2015 and 2016 acaricide efficacy trial conducted in South Carolina, USA. Arrows indicate dates of acaricide applications. Treatments with the same letter within a date are not statistically different (lsmeans P> 0.05). "ns" indicates that the overall model was not significant. The dotted line represents the action threshold for spider mites in tomato (2 per leaflet).
Fig. 2 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 2. Mean (± SE) cumulative mite d of Tetranychus urticae in a 2015 and 2016 acaricide efficacy trial conducted in South Carolina, USA. Arrows indicate dates of acaricide applications. Treatments with the same letter within a date are not statistically different (lsmeans P> 0.05). "ns" indicates that the overall model was not significant.
Additive and dose-dependent mixture effects of Flumite 200 (flufenzin, acaricide) and Quadris (azoxystrobin, fungicide) on the reproduction and survival of Folsomia candida (Collembola)
<p> Our model organism was Folsomia candida (Collembola). We aimed to gain information on the toxicity of Quadris (azoxystrobin) and Flumite 200 (flufenzine aka. diflovidazine) on survival and reproduction and whether the animals can mitigate the toxicity with soil and/or food avoidance behaviour. Also, we aimed to test the effect of the mixture of these two pesticides. We used the OECD 232 reproduction test, a soil avoidance test, and a food choice test for both single pesticides and their mixture. We prepared the mixtures based on the concentration addition model, so the 50% effective concentrations (EC50) of the single materials were used as one toxic unit with a constant ratio of the two materials in the mixture. In the end, the measured mixture EC and LC (lethal concentration) values were compared to the estimate of the concentration addition model.</p>
Data from: Prevalence of and potential risk factors for multiple resistance to acaricides in <em>Rhipicephalus (Boophilus) microplus</em> ticks: A survey in the state of Rio Grande do Sul, Brazil
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Comparative Field Trial of a Beer Blend Attractant and Coumaphos Acaricide for Small Hive Beetle Control
<p>Data associated with publication.</p>
Fig. 3 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 3. Median plot damage ratings in a 2016 acaricide efficacy trial conducted in South Carolina, USA. The dashed line indicates the overall median across treatments. Plots were rated on a 1 to 10 scale, with "1" indicating no damage and "10" indicating complete leaf necrosis.
Data from: Fitness costs of key point mutations that underlie acaricide target-site resistance in the two-spotted spider mite Tetranychus urticae
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Microarray analysis of gene expression in acaricide exposed Rhipicephalus (Boophilus) microplus.
GEO Series GSE10171. Rhipicephalus microplus. 20 samples. Type: Expression profiling by array.
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