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48 results for “Mediterranean fruit fly”
Fig. 9 in Area freedom in Mexico from Mediterranean fruit fly (Diptera: Tephritidae): a review of over 30 years of a successful containment program using an integrated area-wide SIT approach
Fig. 9. Numbers of Mediterranean fruit fly transient entries (detections and outbreaks) per month during the years 2011-2013 into the PFA of Marques de Comillas, Chiapas, for the North Transversal Strip–Marques de Comillas (NTS) front.
Fig. 2 in Area freedom in Mexico from Mediterranean fruit fly (Diptera: Tephritidae): a review of over 30 years of a successful containment program using an integrated area-wide SIT approach
Fig. 2. Mediterranean fruit fly pest free areas (PFAs) in Chiapas, Tabasco, Guatemala and Belize, as well as the location of the current containment barrier, infestation fronts and leading edge of the infestation within Guatemala. The white areas to the southwest and southeast represent the Pacific Ocean and the Caribbean Sea, respectively.
Fig. 5 in Area freedom in Mexico from Mediterranean fruit fly (Diptera: Tephritidae): a review of over 30 years of a successful containment program using an integrated area-wide SIT approach
Fig. 5. Location and percentage of Mediterranean fruit fly transient entries into Mexico during 1982-2013.
Fig. 7 in Area freedom in Mexico from Mediterranean fruit fly (Diptera: Tephritidae): a review of over 30 years of a successful containment program using an integrated area-wide SIT approach
Fig. 7. Mediterranean fruit fly fluctuation (based on routine trapping) within suppression areas in Guatemala associated with El Niño/Southern Oscillation weather events and the population suppression effects of Hurricane Stan and Hurricane Agatha.
Fig. 1 in Exposure to tea tree oil enhances the mating success of male Mediterranean fruit flies (Diptera: Tephritidae)
Fig. 1. Number of matings (mean ± SE) obtained per replicate by wild-like medfly males exposed to TTO (treated) or not exposed (control) for the 3 different TTO concentrations provided to the treated males (the 5% and 50% doses represent TTO concentration [v/v] in a hexane solution). Bar heights represent averages; whiskers represent 1 SE. Results of t-tests: 5% solution: t = 4.8, P <0.001; 50% solution: t = 3.4, P = 0.003; pure (100%): t = 3.8, P <0.001; N = 12 replicates at each concentration.
Figure 2 in Rearing Fopius arisanus (Sonan) (Hymenoptera: Braconidae) on Mediterranean Fruit Fly and its Introduction into Senegal against Oriental Fruit Fly (Diptera: Tephritidae)
Figure 2. Mean (± SEM) numbers of B. dorsalis per kg and mean (± SEM) percent parasitism by F. arisanus from samples of mango and orange sampled from twelve locations between May 2012 and August 2014*.
Figure 1 in Rearing Fopius arisanus (Sonan) (Hymenoptera: Braconidae) on Mediterranean Fruit Fly and its Introduction into Senegal against Oriental Fruit Fly (Diptera: Tephritidae)
Figure 1. Twelve mango and orange sampling sites in the Casamance region of Senegal, with percent parasitism at each site in 2014.
Figure 4 in Capture of Mediterranean Fruit Flies and Melon Flies (Diptera: Tephritidae) in Food-Baited Traps in Hawaii
Figure 4. Numbers of female and male C. cucurbitae captured in Multilure traps baited with torula yeast/borax pellets (TY) or Ceratrap (CT) over the 6-week sampling period in January–February 2015. Bar heights represent averages of 15 traps per bait type; whiskers represent + 1 SE.
Figure 4 in Microsatellite based genetic diversity of Mediterranean fruit fly (Ceratitis capitata, Diptera: Tephritidae) populations from Southwest Turkey
Figure 4. ΔK distribution along with different values of clusters (K) for 7 populations depending on Evanno's method (Evanno et al. 2005) using Structure Harvester application.
Figure 2 in Microsatellite based genetic diversity of Mediterranean fruit fly (Ceratitis capitata, Diptera: Tephritidae) populations from Southwest Turkey
Figure 2. Unrooted Neighboor-Joinning (NJ) tree of 7 C. capitata populations using 8 polymorphic microsatellite markers.
Fig. 1 in Distant-dependent capture probabilities of Mediterranean and oriental fruit flies (Diptera: Tephritidae) in a food-based trap in a Hawaiian mango orchard
Fig. 1. Number of captures (A) and percentage of captures (B: captures divided by released) for Bactrocera dorsalis released from 5, 10, or 20 m from a centrally located trap baited with torula yeast borax solution. For a given replicate, 200 individuals of each sex were released. Symbols represent means with standard error (N = 7 replicates in all cases). Within each sex, numbers of captures differed significantly between distances marked with different upper case letters. Within a distance, numbers of captures differed significantly between the sexes if marked with different lower case letters.
Fig 2 in Relationship between field captures of Mediterranean fruit flies (Diptera: Tephritidae) and the residual amount and release rate of trimedlure from polymeric plugs
Fig 2. Captures of male medflies, Ceratitis capitata, in traps baited with fresh liquid trimedlure or weathered trimedlure plugs over the 12-wk study period in Florida in 2020 (top; means ± SE, N = 12 per treatment) and trimedlure content (means ± SD) and release rate from plugs over the study period (bottom, N = 5 per parameter).
Fig. 1 in Relationship between field captures of Mediterranean fruit flies (Diptera: Tephritidae) and the residual amount and release rate of trimedlure from polymeric plugs
Fig. 1. Captures of male medflies, Ceratitis capitata, in traps baited with fresh liquid trimedlure or weathered trimedlure plugs over the 10-wk study period in Hawaii in 2018 (top; means ± SE, N = 12 per treatment) and trimedlure content (means ± SD) and release rate from plugs over the study period (bottom, N = 5 per parameter).
Figure 1 in Microsatellite based genetic diversity of Mediterranean fruit fly (Ceratitis capitata, Diptera: Tephritidae) populations from Southwest Turkey
Figure 1. Map of Turkey with sampling sites.
Data from: Contribution of maternal effects to dietary selection in Mediterranean fruit flies.
Individual responses to dietary variation represent a fundamental component of fitness, and nutritional adaptation can occur over just a few generations. Maternal effects can show marked proximate responses to nutrition, but whether they contribute to longer-term dietary adaptation is unclear. Here we tested the hypotheses that maternal effects: (i) contribute to dietary adaptation, (ii) diminish when dietary conditions are constant between generations, (iii) are trait-specific and (iv) interact with high- and low-quality food. We used experimental evolution regimes in the medfly (Ceratitis capitata) to test these predictions by subjecting an outbred laboratory-adapted population to replicated experimental evolution on either constant high calorie sugar ('A') or low-calorie starch ('S') larval diets, with a standard adult diet across both regimes. We measured the contribution of maternal effects by comparing developmental and adult phenotypes of individuals reared on their own diet with those swapped onto the opposite diet for either one or two generations (high and low maternal effect conditions, respectively), both at the start and after 30 generations of selection. Initially, there were strong maternal effects on female body mass and male mating success but not larval survival. Interestingly, the initial maternal effects observed in female body mass and male mating success showed sex-specific interactions when individuals from high calorie regimes were tested on low calorie diets. However, as populations responded to selection, the effects of maternal provisioning on all traits diminished. The results broadly supported the predictions. They show how the contribution of maternal effects to dietary responses evolves in a context-dependent manner, with significant variation across different fitness-related traits. We conclude that maternal effects can evolve during nutritional adaptation and hence may be an important life history trait to measure, rather than to routinely minimise.
Figure 2 in Detection of Male Mediterranean Fruit Flies (Diptera: Tephritidae): Performance of Trimedlure Relative to Capilure and Enriched Ginger Root Oil
Figure 2. Capture of C. capitata males in TML- versus EGRO-baited Jackson traps for a single replicate in an Oahu coffee field. Abscissa represents period of lure ageing, where 0 weeks represents fresh lures. Bar heights indicate mean of 20 traps per lure type; error bars represent + 1 SE. Symbols above bars show results of the Tukey HSD test comparing the 2 lures for each ageing category, where an asterisk indicates P <0.001 and ns indicates no significant difference.
Fig. 3 in Area freedom in Mexico from Mediterranean fruit fly (Diptera: Tephritidae): a review of over 30 years of a successful containment program using an integrated area-wide SIT approach
Fig. 3. Location and distance of the leading edge of the Mediterranean fruit fly infestation for the 3 infestation fronts: North Transversal Strip - Marques de Comillas (NTS), Northwest-Comalapa (NW) and Southwest-Soconusco (SW)) in relation to the limits of the pest free areas (PFA) in Chiapas, Mexico for the years 2004-2013. The contour lines of are equidistant 20 km apart and are used as a reference of the distance between the leading edge of the infestation and the limits of the PFA.
Fig. 1 in Area freedom in Mexico from Mediterranean fruit fly (Diptera: Tephritidae): a review of over 30 years of a successful containment program using an integrated area-wide SIT approach
Fig. 1. Schematic representation of the Pest Free Area (PFAs) in Mexico and in the Containment Barrier in Guatemala, with its 3 working areas: the Eradication or Low Pest Prevalence Area (LPA) (2a), the Suppression Area (2b) and the Monitoring Area (2c). The Mediterranean fruit fly pressure is from the east and the south toward the west and the north, with the leading edge of the pest population infestation located at some point within the suppression area along the 3 main infestation fronts as described in the text. The case is shown where the border between Mexico and Guatemala is the limit of the PFA; however, in years of high pest pressure the barrier was partially moved into the PFAs of Chiapas and Tabasco, while in favorable years the PFA in Guatemala grew an annual average of 20-30 km with the containment barrier being moved away from the Mexico-Guatemala border.
Fig. 2 in Exposure to tea tree oil enhances the mating success of male Mediterranean fruit flies (Diptera: Tephritidae)
Fig. 2. Number of matings (mean ± SE) obtained per replicate by wild-like medfly males exposed to TTO (treated) or not exposed (control) for 3 different post-exposure (pre-test) intervals for the treated males (exposed to 200 µL of 5% TTO on an uncovered wick for 1 h). Bar heights represent averages; whiskers represent 1 SE. Results of t-tests: 1 d: t = 4.8, P <0.001; 3 d: t = 2.4, P = 0.03; 5 d: t = 0.6, P = 0.53.
Fig. 3 in Exposure to tea tree oil enhances the mating success of male Mediterranean fruit flies (Diptera: Tephritidae)
Fig. 3. Number of matings obtained per replicate by tsl males and wild-like males where tsl males were or were not exposed to TTO and tested either 1 d (A) or 3 d (B) afer exposure. Wild-like males were not exposed to the chemical in any trial. Bar heights represent averages; whiskers represent 1 SE. Results of t-tests: (A) 1 d post-exposure interval: treated tsl males t = 1.2, P = 0.24; nonexposed tsl males t = 6.8, P <0.001; (B) 3 d post-exposure interval: treated tsl males t = 7.4, P <0.001; non-exposed tsl males t = 6.6, P <0.001.
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