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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).

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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 Sublethal effects of cyflumetofen and spirodiclofen on biological parameters of citrus red mite, Panonychus citri McGregor (Acari: Tetranychidae)

Figure 2. Age-stage specific survival rate (Sxj) of offspring from P. citri females treated with LC20 sublethal concentration of cyflumetofen and spirodiclofen compared with untreated females.

Figure 1 in First DNA-barcode for the genus Aegyptobia (Trombidiformes: Tenuipalpidae) and molecular barcodes of spider mites (Trombidiformes: Tetranychidae) from Iran

Figure 1. Neighbor-Joining tree of the COI sequences using Tamura-Nei model. Scale bar represents number of nucleotide substitutions per site. Bootstrap was 1000 replicates. Numbers on nodes represent bootstrap values.

Figure 2 in Economic injury level of date spider mite, Oligonychus afrasiaticus (Acari: Tetranychidae) on six commercial date cultivars

Figure 2. Regression between mite-day as an independent variable and fruits injury rate as a dependent variable in the different date cultivars studied in 2018.

Figure 3 in Sublethal effects of cyflumetofen and spirodiclofen on biological parameters of citrus red mite, Panonychus citri McGregor (Acari: Tetranychidae)

Figure 3. Age-stage life expectancy (exj) of offspring from P. citri females treated with LC20 sublethal concentration of cyflumetofen and spirodiclofen compared with untreated females.

Figure 7 in Within-tree distribution and seasonal dynamics of Eutetranychus banksi and Euseius stipulatus (Acari: Tetranychidae, Phytoseiidae) on citrus: Implications for the biological control of the pest

Figure 7 Mean proportion of phytoseiids per leaf outside or inside the canopy (a), on the adaxial or abaxial side of the leaves (b), white or red coloured (c), and collected on fruits (d), whenE. banksi occurred or was absent. Capped bars represent ± standard error (SE). Significant differences are denoted with asterisks. Chi square contingency test:P <0.001.

Figure 1 in Within-tree distribution and seasonal dynamics of Eutetranychus banksi and Euseius stipulatus (Acari: Tetranychidae, Phytoseiidae) on citrus: Implications for the biological control of the pest

Figure 1 Mean number ofE. banksi(a–d) and phytoseiid mites (e–h) per leaf or per cm2 of leaves and fruits. Capped bars represent ± standard error (SE). Bars with different letters are significantly different (Wilcoxon rank-sum test).

Figure 5 in Within-tree distribution and seasonal dynamics of Eutetranychus banksi and Euseius stipulatus (Acari: Tetranychidae, Phytoseiidae) on citrus: Implications for the biological control of the pest

Figure 5 (a–d) Representation of the binomial (logit-link) generalized linear models (GLMs) showing the relationship between the proportion

Figure 3 in Within-tree distribution and seasonal dynamics of Eutetranychus banksi and Euseius stipulatus (Acari: Tetranychidae, Phytoseiidae) on citrus: Implications for the biological control of the pest

Figure 3 Seasonal relative abundance of motile forms of phytoseiid species in four (2018) and six (2019) citrus orchards. Percentage of each species per sampling is represented. The summer decline

Figure 4 in Within-tree distribution and seasonal dynamics of Eutetranychus banksi and Euseius stipulatus (Acari: Tetranychidae, Phytoseiidae) on citrus: Implications for the biological control of the pest

Figure 4 Variation in the spatial distribution and body coloration of phytoseiid in relation to the abundanceE. of banksi in four (2018) and six (2019) citrus orchards. Grey bars indicate the percentage of phytoseiids collected outside the canopy, on the leaf adaxial sides, fruits occupied by phytoseiids, and red phytoseiids (primary y-axis), in relation with the mean numberE of. banksi per leaf or fruit represented as a solid line (secondary, y-axis). Capped bars represent ± standard error (SE).

Figure 2 in Within-tree distribution and seasonal dynamics of Eutetranychus banksi and Euseius stipulatus (Acari: Tetranychidae, Phytoseiidae) on citrus: Implications for the biological control of the pest

Figure 2 Seasonal trends ofE. banksi and phytoseiid mites on leaves (solid line, first y-axis) and fruits (broken line, second y-axis) in four and six citrus orchards in 2018 and 2019 respectively. Mean number of mites collected per sampling unit (all the stages were pooled together). Note that first and second y-axis scales are different. Mean (solid line), maximum and minimum daily temperatures in °C (broken lines) and mean daily relative humidity (RH) were represented.