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447 results for “Urtica”
Fig. 3 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 3. Number (mean ± SE) of live females (A, C2 = 31.11; df = 37; P = 0.259), immature individuals (B, C2 = 27.67; df = 37; P = 0.133), eggs (C, C2 = 27.67; df = 36; P = 0.240), and dead females (D, C2 = 23.58; df = 37; P = 0.042) of the two-spotted spider mite Tetranychus urticae on infested conventional (30F35) (white bars) and Bt (30F35Hx) (gray bars) maize plants. ns = statistically insignificant, * = statistically significant (P <0.05).
Fig. 1 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 1. Number (mean ± SE) of live females (A, C2 = 45.2; df = 36; P = 0.861), immature individuals (B, C2 = 38.7; df = 37; P = 0.608), eggs (C, C2 = 38.1; df = 36; P = 0.624), and dead females (D, C2 = 29.7; df = 37; P = 0.203) of the two-spotted spider mite Tetranychus urticae on clean (white bars) and co-specific re-infested (gray bars) conventional maize plants (30F35). ns = statistically insignificant.
Fig. 7 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 7. Projection to principal component analysis based on the ions detected by electrospray ionization mass spectrometry of uninfested (C = o) and infested with Tetranychus urticae (C + Tu = ●) conventional maize; uninfested (Bt = Z) and infested with T. urticae (Bt + Tu = ■) Bt maize; infested with T. urticae and Spodoptera frungiperda (C + Tu + Sf = Δ) conventional maize; and infested with T. urticae and S. frungiperda (Bt + Tu + Sf = ▲) Bt maize, using the first 2 principal components (Dim) with explained variance in brackets
Fig. 2 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 2. Number (mean ± SE) of live females (A, C2 = 21.9; df = 37; P = 0.02), immature individuals (B, C2 = 40.9; df = 37; P = 0.698), eggs (C, C2 = 30.5; df = 37; P = 0.235), and dead females (D, C2 = 21.9; df = 37; P = 0.383) of the two-spotted spider mite, Tetranychus urticae, on clean (light gray bars) and co-specific re-infested (dark gray bars) Bt maize plants (30F35Hx). ns = statistically insignificant, * = statistically significant (P <0.05).
Fig. 2 in Resistance of four rose varieties to Tetranychus urticae (Acari: Tetranychidae) under greenhouse conditions
Fig. 2. Average (± SE) of the percentage of chlorophyll loss caused by the feeding of Tetranychus urticae. Varieties with different letters were significantly different (Tukey test, P <0.05).
Fig. 1 in Resistance of four rose varieties to Tetranychus urticae (Acari: Tetranychidae) under greenhouse conditions
Fig. 1. Box-plot comparing growth rate (r) of Tetranychus urticae on 4 rose varieties. Varieties with different letters were significantly different (Nemenyi test, P <0.05).
Figure 3 in Seasonal abundance of Tetranychus urticae and Amblyseius swirskii (Acari: Tetranychidae and Phytoseiidae) on four strawberry cultivars
Figure 3. Overall mean numbers of Tetranychus urticae and Amblyseius swirskii on four strawberry cultivars during (a) 2017/2018 and (b) 2018/2019 seasons.
Figure 1 in Seasonal abundance of Tetranychus urticae and Amblyseius swirskii (Acari: Tetranychidae and Phytoseiidae) on four strawberry cultivars
Figure 1. Mean numbers of Tetranychus urticae and Amblyseius swirskii populations on four strawberry cultivars during 2017/2018 season.
Figure 2 in Seasonal abundance of Tetranychus urticae and Amblyseius swirskii (Acari: Tetranychidae and Phytoseiidae) on four strawberry cultivars
Figure 2. Mean numbers of Tetranychus urticae and Amblyseius swirskii populations on four strawberry cultivars during 2018/2019 season.
Figure 2 in On the effect of ozonated water on mortality of Tetranychus urticae (Trombidiformes: Tetranychidae) on Capsicum annuum (Solanaceae) in greenhouse conditions
Figure 2. The effect of ozone concentrations (0 and 43 g/m3) on mortality rate (mean ± SE) of T. urticae on pepper (Capsicum annuum L.) in a controlled environment.
Figure 3 in On the effect of ozonated water on mortality of Tetranychus urticae (Trombidiformes: Tetranychidae) on Capsicum annuum (Solanaceae) in greenhouse conditions
Figure 3. The effect of age of the plant (4, 8 and 12 weeks old) on mortality rate (mean ± SE) of T. urticae on pepper (Capsicum annuum L.) at 0 and 43 g/m3 ozone concentration in a controlled environment.
Figure 1 in On the effect of ozonated water on mortality of Tetranychus urticae (Trombidiformes: Tetranychidae) on Capsicum annuum (Solanaceae) in greenhouse conditions
Figure 1. Interaction effect between ozone concentration (0 and 43 g/m3) and exposure time (5, 10 and 15 s) on mortality percentage (mean ± SE) of T. urticae on pepper (Capsicum annuum L.) in a controlled environment.
Figure 1 in Effects of temperature on a Chinese population ofAmblyseius andersoni (Acari: Phytoseiidae) fed with Tetranychus urticae
Figure 1 Age-specific survival rate (lx) and age-specific fecundity ratem(x) curves of female Ambl- yseius andersoni at five different temperatures. —▲— Age-specific survival rate (lx). —■— Age- specific fecundity rate (mx).
Figure 2 in Effect of the essential oil from the latex of the fruit Mangifera indica L. on Tetranychus urticae Koch (Acari, Tetranychidae)
Figure 2 Egg laying preference (mean ± SE) ofTetranychus urticaeexposed toMangifera indica oils and selected constituents for 48 hours. *significantly different (p<0.05).
Figure 3 in Suitability of different pollen grains and Tetranychus urticae as food for the predatory mite, Amblyseius swirskii (Acari: Phytoseiidae)
Figure 3. Pollen shape of eight different plant pollens prepared using a Scanning Electron Microscopy (SEM).
Figure 2 in Suitability of different pollen grains and Tetranychus urticae as food for the predatory mite, Amblyseius swirskii (Acari: Phytoseiidae)
Figure 2. Age-specific survivorship (lx), and age-stage-specific fecundity (fxj) of Ambluseius swirskii fed on Tetranychus urticae and seven different plant pollen grains.
Figure 1 in Biological effects of three bacterial species on Tetranychus urticae (Acari: Tetranychidae) infesting eggplant under laboratory and greenhouse conditions
Figure 1 Pictures of dead mite individuals after spray with the pathogenic bacteria: A – Acinetobacter sp.; B –B. subtilis and C –B. qassimus
Figure 2 in Silicon derivatives induced host plant resistance against Tetranychus urticae (Acari: Tetranychidae) in eggplants farms
Figure 2. (A) Silicon leaf, total protein and phenol contents, (B) Activity of POD, CAT, and PPO of S. melongena- treated plants. Means followed by the same letter are not significantly different using Tukey's HSD Test at P <0.05. T1 = Control, T2 = OSAB 2 mL L−1, T3= OSAB 4 mL L−1, T4= Silica K 2 mL L−1, and T5 = Silica K 4 mL L−1.
Figure 1 in Silicon derivatives induced host plant resistance against Tetranychus urticae (Acari: Tetranychidae) in eggplants farms
Figure 1. Mean number ± SE of the different stages of T. urticae on S. melongena leaves 10, 30 and 50 days after spraying (DAS). Means followed by the same letter are not significantly different using Tukey's HSD at P <0.05. T1 = Control, T2 = OSAB 2 mL L−1, T3 = OSAB 4 mL L−1, T4 = Silica K 2 mL L−1, and T5 = Silica K 4 mL L−1.
Figure 1 in Alfalfa responses to drought, salinity, and herbivory by Tetranychus urticae (Acari: Tetranychidae) and performance of the pest on water-stressed plants
Figure 1. Effects of drought stress on proline content of alfalfa plants before and after Tetranychus urticae feeding. Within each column mean (± SE) followed by the same letter(s) are not significantly different. Capital letters show the effect of drought.
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