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1,084 results for “Tortricidae”
Figure 4 in Epiblema minutana (Lepidoptera, Tortricidae) in Israel: Promise or Peril?
Figure 4. Preliminary fundamental host range of Epiblema minutana (y-axis) (different letters indicate significant differences at p <0.05; Kruskal-Wallis test)."H. annuus CF" = Helianthus annuus "Clearfield", "H. annuus O" = Helianthus annuus "Orange Fire".
Figure 2 in Epiblema minutana (Lepidoptera, Tortricidae) in Israel: Promise or Peril?
Figure 2. Altitude of sites with host plants (confirmed by no-choice experiments) surveyed. Plots depict number of sites with Epiblema minutana galls (dotted lines) or without (solid lines).
Figure 1 in Effect of a short-cycle apple tree cultivar on oriental fruit moth (Lepidoptera: Tortricidae) development and larval behavior
Figure 1. Average number of Grapholita molesta males captured monthly by pheromone-bait traps in 'Eva' and 'Gala' apple orchards during seven years in Porto Amazonas, Paraná, Brazil.
Figs. 7-9.- Genitalias. 7 in Contribución al conocimiento de los microlepidópteros de España (Lepidoptera: Tortricidae, Pyralidae).
Figs. 7-9.- Genitalias. 7.- Dichrorampha chavanneana (De La Harpe, 1858). (prep. genit. 5873JG). 8.- Ancylis obtusana (Haworth, [1811]), (prep. genit. 6038JG). 9.- Eucosma fervidana (Zeller, 1847) (prep. genit. 5852JG).
Figs. 3-4.- Genitalias. 3 in Pelochrista lugubrana Treitschke, 1830, nuevo Olethreutinae para la Península Ibérica (Lepidoptera: Tortricidae).
Figs. 3-4.- Genitalias. 3.- Pelochrista lugubrana Treitschke, 1830 (prep. genit. 5788JG). 4.- Epinotia dalmatana (Rebel, 1891) (prep. genit. 5787JG).
Figs. 10-12.- Genitalias. 10 in Seis especies nuevas de microlepidópteros para España (Lepidoptera: Tortricidae).
Figs. 10-12.- Genitalias. 10.- Pammene rhediella (Clerck, 1759), prep. genit. 5767JG. 11.- Rhopobota myrtillana (Humphreys & Westwood, 1845), prep. genit. 5768JG. 12.- Grapholita jungiella (Linnaeus, 1761), prep. genit. 5765JG.
Figs. 7-9.- Genitalias. 7 in Seis especies nuevas de microlepidópteros para España (Lepidoptera: Tortricidae).
Figs. 7-9.- Genitalias. 7.- Acleris roscidana (Hübner, [1796-99]), prep. genit. 5759JG. 8.- Apotomis semifasciana (Haworth, [1811]), prep. genit. 5760JG. 9.- Grapholita lobarzebskii (Nowicki, 1860), prep. genit. 5766JG.
Fig. 5 in Methods to separate Lobesia botrana (Lepidoptera: Tortricidae) males from females for the implementation of sterile insect-inherited sterility technique control tactics
Fig. 5. The percentages of male and female Lobesia botrana adults that emerged from the pupal stage on each consecutive d afer the onset of adult emergence.
Fig. 6 in Methods to separate Lobesia botrana (Lepidoptera: Tortricidae) males from females for the implementation of sterile insect-inherited sterility technique control tactics
Fig. 6. Distribution of Lobesia botrana male and female pupae based on the overall lengths of the pupae.
Fig. 3. R, G and B in Methods to separate Lobesia botrana (Lepidoptera: Tortricidae) males from females for the implementation of sterile insect-inherited sterility technique control tactics
Fig. 3. R, G and B color values of male and female Lobesia botrana larvae during the wandering phase. A. Average R, G and B color values of wandering male and female larvae, and B. Percentages of wandering red, green and blue larvae in relation to the R, G and B values as a proportion of total male and female larvae. * P = 0.001, Tukey α = 0.05.
Fig. 1 in Methods to separate Lobesia botrana (Lepidoptera: Tortricidae) males from females for the implementation of sterile insect-inherited sterility technique control tactics
Fig. 1. Lobesia botrana pupae indicating the number of abdominal segments in (A) male (4 segments), and (B) female pupae (3 segments) as measured from the abdomen tip to the wing's point, and (C) distance between the head and the abdomen tip as a measurement of pupal length.
Fig. 2 in Flight ability and dispersal of European grapevine moth gamma-irradiated males (Lepidoptera: Tortricidae)
Fig. 2. Schematic representation of the vineyard and the pheromone traps positions at the experimental plot where the marked male moths were released.
Fig. 4 in Methods to separate Lobesia botrana (Lepidoptera: Tortricidae) males from females for the implementation of sterile insect-inherited sterility technique control tactics
Fig. 4. The percentages of wandering Lobesia botrana larvae that departed from their food on each consecutive day of the wandering phase and that sub- sequently developed into either adult males or adult females.
Fig 1 in Flight ability and dispersal of European grapevine moth gamma-irradiated males (Lepidoptera: Tortricidae)
Fig 1. Schematic representation of the flight assessment cage used to measure the flight responses of Lobesia botrana males to calling females. In the female compartment, 2-day-old virgin females were confined inside a small cylindrical plastic mesh box with a 5% sucrose-wetted wick. Males irradiated either with 150 Gy or with 350 Gy and untreated males differentially marked with variously colored fluorescent powders were introduced into the male compartment. The number of males of each of the 3 kinds that flew through the open slit at the 45 cm height [the 2 lower openings (slits) were sealed] into the female compartment were recorded at 24, 48, 72 and 96 h. Air was drawn into the female compartment and exhausted from the male compartment.
Fig. 3 in Limited gene flow among Cydia pomonella (Lepidoptera: Tortricidae) populations in two isolated regions in China: Implications for utilization of the SIT
Fig. 3. Dendrogram generated by NJ analysis representing the genetic distance among populations of Cydia pomonella. The topology was tested by bootstrap analysis with 1,000 replicates. The scale bar represents 2.0% genetic distance. The sampling locations include JinTa (JJT), YinDa (JYD), XiDong (JXD) and ZongZai (JZZ) of Jiuquan Region, and Luo Tuocheng (ZLT), NiJiaying (ZNJ), MinYong (ZMY) and XiaoMan (ZXM) of Zhangye Region.
Fig. 1 in Limited gene flow among Cydia pomonella (Lepidoptera: Tortricidae) populations in two isolated regions in China: Implications for utilization of the SIT
Fig. 1. Sampling regions and locations of Cydia pomonella in Hexi Corridor of China. (I) map of China, the Hexi Corridor is indicated in the dash box; (II) enlarged map of Hexi Corridor, the 2 sampling regions are indicated as (A) Jiuquan region and (B) Zhangye region; (III) enlarged map of the sampling regions and sampling locations. The sampling locations includes JinTa (JJT), YinDa (JYD), XiDong (JXD), and ZongZai (JZZ) of the Jiuquan Region, and Luo Tuocheng (ZLT), NiJiaying (ZNJ), MinYong (ZMY) and XiaoMan (ZXM) of the Zhangye Region.
Fig. 2 in Limited gene flow among Cydia pomonella (Lepidoptera: Tortricidae) populations in two isolated regions in China: Implications for utilization of the SIT
Fig. 2. Bayesian clustering analysis by use of STRUCTURE, which indicates the presence of 2 clusters. Proportion of membership coefficient for 8 Cydia pomonella populations falling into the 2 clusters is depicted by 2 different shades of gray, respectively. The sampling locations include JinTa (JJT), YinDa (JYD), XiDong (JXD) and ZongZai (JZZ) of Jiuquan Region, and Luo Tuocheng (ZLT), NiJiaying (ZNJ), MinYong (ZMY) and XiaoMan (ZXM) of Zhangye Region.
Fig. 1 in Effect of genetically modified Bt maize in an artificial diet on the survival of Cydia pomonella (Lepidoptera: Tortricidae)
Fig. 1. Probit response on log Bt concentration of Cydia pomonella larvae reared on a diet containing maize where the responses were: (A) larval mortality Y = 2.980 + 1.27(X); (B) delayed larval development, Y = 3.789 + 1.886(X) for experiment 1 and Y = 2.840 + 1.886(X) for experiment 2; (C) larvae leaving the diet, Y = 3.595 + 0.681(X); (D) total response or response A + B + C, Y = 4.133 + 2.344(X) for experiment 1 and Y = 3.592 + 2.344(X) for experiment 2. Y is the probit response and X is the log Bt concentration.
Fig. 6 in Influence of holding temperature and irradiation on field performance of mass-reared Thaumatotibia leucotreta (Lepidoptera: Tortricidae)
Fig. 6. Comparison of an insectary air-stream coLLection system and postcoLLection chiLLing (8 ± 1 °C) to manuaL coLLection without chiLLing (25 ± 1 °C) on the mean number of male Thaumatotibia leucotreta moths recaptured in pheromone traps afer reLease in a citrus orchard during Jan 13 and Apr 7, 2014.
Fig. 1 in Influence of holding temperature and irradiation on field performance of mass-reared Thaumatotibia leucotreta (Lepidoptera: Tortricidae)
Fig. 1. Diagram of a 5-ha naveL orange orchard showing the centraL reLease site (X) for Thaumatotibia leucotreta moths and the pheromone trap placement. The distance (m) from the center release site to each trap is listed at the right of the diagram.
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International Brain Laboratory public data
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OpenNeuro
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