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153 results for “Tetranychus urticae”
Figure 5 in Evaluation of geostatistical method and hybrid Artificial Neural Network with imperialist competitive algorithm for predicting distribution pattern of Tetranychus urticae (Acari: Tetranychidae) in cucumber field of Behbahan, Iran
Figure 5. Moving colonies to imperialist in culture and language axes (AtashpazGargari et al. 2008).
Figure 2 in Evaluation of geostatistical method and hybrid Artificial Neural Network with imperialist competitive algorithm for predicting distribution pattern of Tetranychus urticae (Acari: Tetranychidae) in cucumber field of Behbahan, Iran
Figure 2. Generalized semivariogram showing the range of spatial dependence, nugget effect (C0) variability associated with spatial dependence (C), and sill (C + C0).
Figure 5 in Hybrid neural network with genetic algorithms for predicting distribution pattern of Tetranychus urticae (Acari: Tetranychidae) in cucumbers field of Ramhormoz, Iran
Figure 5. Tetranychus urticae distribution maps in actual (b, d and f) and classified conditions by MLPNN (c, e and a). The maps of a, c, e and b, d, f have been drawn according to economic threshold of 4, 8 and 12, respectively.
Figure 4 in Daily consumption and functional response of Stethorus gilvifrons (Coleoptera: Coccinellidae) and Orius albidipennis (Hemiptera: Anthocoridae) to Tetranychus urticae (Acari: Tetranychidae)
Figure 4. Proportion of T. urticae eggs consumed by adults of: a) O. albidipennis, b) S. gilvifrons, when provided by different prey densities.
Figure 3 in Daily consumption and functional response of Stethorus gilvifrons (Coleoptera: Coccinellidae) and Orius albidipennis (Hemiptera: Anthocoridae) to Tetranychus urticae (Acari: Tetranychidae)
Figure 3. Proportion of T. urticae eggs consumed by immatures of: a) O. albidipennis, b) S. gilvifrons, when provided by different prey densities.
Figure 2 in Daily consumption and functional response of Stethorus gilvifrons (Coleoptera: Coccinellidae) and Orius albidipennis (Hemiptera: Anthocoridae) to Tetranychus urticae (Acari: Tetranychidae)
Figure 2. Proportion of T. urticae protonymphs consumed by different life stages of: a) O. albidipennis, b) S. gilvifrons, when provided by different prey densities.
Figure 1 in Daily consumption and functional response of Stethorus gilvifrons (Coleoptera: Coccinellidae) and Orius albidipennis (Hemiptera: Anthocoridae) to Tetranychus urticae (Acari: Tetranychidae)
Figure 1. Proportion of T. urticae females consumed by different life stages of: a) O. albidipennis, b) S. gilvifrons, when provided by different prey densities.
Figure 1 in Laboratory evaluation of Beauveria bassiana, some plant oils and insect growth regulators against two-spotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae)
Figure 1. Infection caused by Beauveria bassiana on Tetranychus urticae, (a, b) dead female mites due to mycosis, (c) dead mite in control.
Figure 5 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea
Figure 5. The relationship between UV Aerosol Index extracted from Sentinel-5 imagery and spider mite population (mean score of each window) from June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite distribution data).
Figure 6 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea
Figure 6. The relationship between daily CHIRPS-precipitation and spider mite population (mean score of each window) from June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite distribution data).
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.
Figure 9 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea
Figure 9. The relationship between NDVI (10 m) provided form Sentinal-2 and density of spider mite during monitoring windows based on ANOVA for linear regression. The alphabetical letters indicate of the sequence windows from June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite distribution data).
Figure 4 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea
Figure 4. Distribution maps of spider mite based on IDW model during monitoring windows, a–n are the sequence windows form June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite population data).
Figure 1 in Use of homeophathic preparations for red spider mite, Tetranychus urticae (Acari: Tetranychidae) control in strawberry plants
Figure 1. Degree of a) Incidence, and b) severity caused by T. urticae in strawberry plants 30 and 60 days after applying the treatments: Distilled water (Ctl); 6 and 30 CH Strawberry leaves homeopathic (Agroh); 6 and 30 CH Bovista (Bov); 6 and 30 CH Belladonna (Bellad); 6 and 30 CH Arnica (Árni) and 6 and 30 CH Ferrum sulphuricum (FS). Treatments with the same letter are not significantly different between them (p <0.05) (n = 8).
Figure 8 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea
Figure 8. The relationship between MODIS-Evapotranspiration and spider mite population (mean score of each window) from June 9, 2020 to September 17, 2020. (First window, May 30 to June 9 was not spider mite distribution data).
Figure 1 in Toxicity and ovicidal activity of different entomopathogenic fungi, Hirsutella extracts on Tetranychus urticae (Acari: Tetranychidae)
Figure 1. Accumulated mortality of T. urticae females at 24, 48 and 72 h after being fed with mulberry leaf discs treated with different concentrations of crude extract, six species of Hirsutella under residual effect bioassay. For each extract and mite, means followed by the same letter are not significantly different (p = 0.05; Tukey HDS test).
Figure 3 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea
Figure 3. Spider mite distribution throughout Golestan province; 6 (min.) × 6 (min.) grid cells in the DMS coordinate system (yellow points indicate the monitoring fields).
Figure 2 in The predatory mite Neoseiulus californicus (Acari: Phytoseiidae) does not respond for volatiles of maize infested by Tetranychus urticae (Acari: Tetranychidae)
Figure 2. Olfactory response of Neoseiulus californicus in Y-olfactometer. (A) maize plants without infestation vs. maize plants infested by 100 adult females of T. urticae, (B) maize plants without infestation vs. maize plants infested by 200 adult females of T. urticae and (C) maize plants infested by ten vs. 200 adult females of T. urticae. NR represents non-responsive insects (no choice). Chi-square test with 5% significance. Numbers in bars represent individual predator that choose the indicated odor. The number of predatory mite without response to the treatments (NR), after 5 minutes, was eliminated from the statistical analysis.
Figure 1 in The predatory mite Neoseiulus californicus (Acari: Phytoseiidae) does not respond for volatiles of maize infested by Tetranychus urticae (Acari: Tetranychidae)
Figure 1. Olfactory response of Neoseiulus californicus in Y-olfactometer. (A) air vs. air (white bars), (B) air vs. maize plants without infestation and (C) maize plants without infestation vs. maize plants infested by ten adult females of T. urticae. NR represents nonresponsive insects (no choice). Chi-square test with 5% significance. Numbers in bars represent individual predator that choose the indicated odor. The number of predatory mite without response to the treatments (NR), after 5 minutes, was eliminated from the statistical analysis.
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