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122 results for “Ceratitis”
Fig. 6 in Description of new Ceratitis species (Diptera: Tephritidae) from Africa, or how morphological and DNA data are complementary in discovering unknown species and matching sexes
Fig. 6. Ceratitis serrata De Meyer, 1996. a. Head, frontal view. b. Head and thorax, anterodorsal view. c. Thorax, lateral view. d. Thorax, dorsal view. e. Abdomen, dorsal view. Scale bars: A = 0.5 mm; B–D = 1 mm.
Fig. 3 in Description of new Ceratitis species (Diptera: Tephritidae) from Africa, or how morphological and DNA data are complementary in discovering unknown species and matching sexes
Fig. 3. Ceratitis taitaensis De Meyer & Copeland sp. nov. a. Head and thorax, anterodorsal view. b. Thorax, lateral view. c. Thorax, dorsal view. d. Abdomen, dorsal view. e. Male wing. f. Female wing. g. Female aculeus. h. Aculeus tip. Scale bars: A–F = 1 mm; G–H = 0.1mm.
Fig. 4 in Description of new Ceratitis species (Diptera: Tephritidae) from Africa, or how morphological and DNA data are complementary in discovering unknown species and matching sexes
Fig. 4. Ceratitis sawahilensis De Meyer & Virgilio sp. nov. a. Head and thorax, anterodorsal view. b. Thorax, lateral view. c. Thorax, dorsal view. d. Abdomen, dorsal view. e. Wing. f. Habitus image (credit: S.A. Marshall). g. Female aculeus. h. Aculeus tip. Scale bars: A–F = 1 mm; G–H = 0.1 mm.
Fig. 2 in Description of new Ceratitis species (Diptera: Tephritidae) from Africa, or how morphological and DNA data are complementary in discovering unknown species and matching sexes
Fig. 2. Ceratitis pallidula De Meyer, Mwatawala & Virgilio sp. nov. a. Head and thorax, anterodorsal view. b. Head and thorax, lateral view. c. Thorax, dorsal view. d. Abdomen, dorsal view. e. Wing. Scale bars = 1 mm.
Fig. 1. — a–f in Description of new Ceratitis species (Diptera: Tephritidae) from Africa, or how morphological and DNA data are complementary in discovering unknown species and matching sexes
Fig. 1. — a–f. Ceratitis quilicii De Meyer, Mwatawala & Virgilio sp. nov. Ƌ. a. Head and thorax, anterodorsal view. b. Head and thorax, lateral view. c. Thorax, dorsal view. d. Midleg, anterior view. e. Wing. f. Midtibia, anterior view. — g. C. rosa Karsch, 1887 s.str. midtibia, anterior view. Scale bars = 1 mm.
Quality control traceability during the packing and release process of Ceratitis capitata for Sterile Insect Technique
<p><strong>Abstract</strong></p> <p>In programs applying the Sterile Insect Technique (SIT), the quality of insects deployed in the field determines the success in preventing, suppressing, containing, or eradicating the pest population. In the fruit fly emergence and release facility (ERF) of the Moscamed Program in Mexico, irradiated pupae of <em>Ceratitis capitata</em> are packed in Mexico-type towers, and key adult quality parameters, such as emergence, fliers, and survival, are determined throughout the packing, handling and release process. However, different methodologies are used to estimate the percentage of fliers in the different stages of the process, raising doubts of whether observed differences are due to the effect of each stage or to the methodology used. With this in mind, we developed an alternative called “Adult Flier device” (= AF-device) to evaluate the adult flier parameter following a critical evaluation path of five steps: 1) upon arrival at ERF, 2) post-packing, 3) post-holding, 4) post-chilling, and 5) post-release, where adult fliers and survival under stress were evaluated. We also compared the current methodologies for the estimation of "absolute fliers" available in different operating manuals. Our results suggest that the AF-device allows reliable traceability of sterile insect quality parameters throughout the packing and release process, since no significant differences were observed with the control treatments. In the chilling stage, the five methodologies tested were equivalent, but the AF-device was less time-consuming and required less manpower and biological material than the other methodological options. Our results demonstrate that the use of the AF-device can be a feasible, versatile, innovative, and efficient alternative to evaluate quality control parameters throughout the process of packing and releasing sterile insects, providing reliable results in a timely manner with less hand labor using minimal biological material.</p>
(10)-Strobl2022A-DS0008 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0008 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0004 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0004 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0001 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0001 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0003 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0003 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0002 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0002 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0007 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0007 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0009 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0009 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0006 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0006 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
(10)-Strobl2022A-DS0005 – Ceratitis capitata TREhs43-hid^Ala5_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy
<p>(10)-Strobl2022A-DS0004 – <em>Ceratitis capitata</em> TREhs43-hid<sup>Ala5</sup>_F1m2 long-term live imaging dataset of embryonic development acquired with light sheet fluorescence microscopy</p>
Figure 3 in Spatial distribution of Ceratitis capitata in guava orchards and influences from orchard management
Figure 3. Estimates of the parameters of the regression analysis by the Taylor power model, adjusted by the F test to evaluate the spatial distribution and the t-test to compare the hypotheses of the aggregation index of Ceratitis capitata in guava orchards, Ivinhema-MS. Tests: ANOVA (F = 304.05; p <0.001; g.l = 20); t (5.17; p <0.001) for the Alpha hypothesis (h0: a = 1 vs h1 a ≠ 1, where: Alpha (a <0, a = 0 and a>0) and; t (17.44; p <0.001) for the Beta hypothesis (h0: b = 1 vs h1: b ≠ 1), where: Beta (b <1, b = 1 and b> 1).
Figure 2 in Spatial distribution of Ceratitis capitata in guava orchards and influences from orchard management
Figure 2. Number of fruit fly/trap/day (FTD) of Ceratitis capitata and range of negative binomial thresholds (Bn) with other distributions, establishing the levels of safety and control activities for the Mediterranean fly in three guava orchards, Ivinhema, MS, Brazil.
Figure 1 in Oviposition performance of tephritid polyphagous Anastrepha fraterculus and Ceratitis capitata during three periods of exposure to fruit
Figure 1. Oviposition behaviour of A. fraterculus and C. capitata during three infestation periods of fruit.
Fig. 1 in Oviposition of Anastrepha fraterculus and Ceratitis capitata (Diptera: Tephritidae) in citrus fruits, and development in relation to maturity of orange fruits
Fig. 1. Frequency of oviposition by females of Anastrepha fraterculus (A) and Ceratitis capitata (B) when provided with oranges as an oviposition substrate.
Fig. 1 in Occurrence of Anastrepha fraterculus and Ceratitis capitata (Diptera: Tephritidae) in organically grown Rubus (Rosales: Rosaceae), in two contrasting environments of northwestern Argentina
Fig. 1. Precipitation (P), evapotranspiration (ET), and hydric balance (HB = P − ET) near Monte Grande (27.0000°S, 65.4000°W; 350 m altitude; Tucumán, Argentina) in 2013 (A) and 2014 (B).
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