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435 results for “Sterilization”
Fig. 1 in Inherited sterility in Tuta absoluta (Lepidoptera: Gelechiidae): Pest population suppression and potential for combined use with a generalist predator
Fig. 1. Population suppression by irradiated individuals and their progeny over 12 weeks at a 10:1 irradiated:untreated ratio. a) Number of eggs/ cage, b) number of small larvae /cage and c) number of large larvae/cage (mean ± SE). Only 1 release of irradiated moths was made, i.e., at the beginning of the experiment. For details see text on Experiment 1.
Fig. 3 in Tools and Methods to Assess Field Performance Locomotion activity meter for quality assessment of mass-reared sterile male moths (Lepidoptera)
Fig. 3. Mean activity counts for before and afer pheromone exposure (lef), and the mean afer/before activity ratio (right), for un-irradiated (0 Gy = −) and irradiated (300 Gy = +) Epiphyas postvittana males. Error bars are 95% confidence limits for each mean. An afer/before ratio of 1 (marked) indicates an equal level of activity before and afer pheromone exposure.
Fig. 2 in Tools and Methods to Assess Field Performance Locomotion activity meter for quality assessment of mass-reared sterile male moths (Lepidoptera)
Fig. 2. Measured activity of male Epiphyas postvittana as summed counts at 30 s intervals in a locomotor activity monitor, before and afer pheromone stimulus of irradiated and non-irradiated moths.
Fig. 1 in Tools and Methods to Assess Field Performance Locomotion activity meter for quality assessment of mass-reared sterile male moths (Lepidoptera)
Fig. 1. An illustration of the modified Locomotion Activity Monitor set-up used for the bioassays in this study. Synthetic pheromone was puffed (2 s) from upwind to stimulate LBAM males into wing fanning. Each time a male moved through the beam array it was counted as 1 observation. Comparisons were made between pre-pheromone exposure activity and post-pheromone exposure activity for each treatment.
Fig. 4 in Inherited sterility in Tuta absoluta (Lepidoptera: Gelechiidae): Pest population suppression and potential for combined use with a generalist predator
Fig. 4. Prey consumption in the choice test involving progeny of irradiated males. Number of T. absoluta eggs from following T. absoluta eggs crosses, ♀U × ƋU and ♀U × ƋI,consumed per T. cucurbitaceus (mean ± SE) individual in 24 h. The same letter above the 2 error bars indicates that there was no significant difference in the numbers of eggs consumed based on the crosses from which they had originated, even though the male parent had been irradiated in 1 of the crosses (paired t tests, P> 0.05). U = untreated, I = irradiated.
Fig. 2 in Inherited sterility in Tuta absoluta (Lepidoptera: Gelechiidae): Pest population suppression and potential for combined use with a generalist predator
Fig. 2. Population suppression by irradiated individuals and their progeny over 12 weeks at a 15:1 irradiated:untreated ratio. a) Number of eggs/cage, b) number of small larvae /cage and c) number of large larvae/cage (mean ± SE). Only 1 release of irradiated moths was made, i.e., at the beginning of the experiment. For details see text on Experiment 2.
Fig. 4 in Tools and Methods to Assess Field Performance Locomotion activity meter for quality assessment of mass-reared sterile male moths (Lepidoptera)
Fig. 4. Mean activity counts for before and afer pheromone exposure (lef), and the mean afer/before activity ratio (right), un-irradiated (0 Gy) and irradiated (300 Gy) Epiphyas postvittana males exposed to 1 of 4 levels of temperature shock (0, 1, 2, 4 h at 30 °C). Error bars are 95% confidence limits for each mean. An afer/before ratio of 1 (marked) indicates an equal level of activity before and afer pheromone exposure.
Fig. 3 in Performance improvement through quality evaluations of sterile cactus moths, Cactoblastis cactorum (Lepidoptera: Pyralidae), mass-reared at two insectaries
Fig. 3. The mean percentage increase in mating of Cactoblastis cactorum females in mating cage bioassays as influenced by the insectary (DPI or TIF) and the trial conducted before (trial 1) and afer (trial 2) quality improvements were made to the rearing and handling protocols at the DPI insectary. Vertical bars denote 0.95 confidence intervals.
Fig. 7 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs
Fig. 7. Isotope signatures of the European grapevine moth, Lobesia botrana; error bars are 2 standard deviations of the mean.
Fig. 1 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs
Fig. 1. Percentage of sucrose based on dry weight (DW) in popular artificial diets for mass rearing various moth species, as described by Dyck (2010).
Fig. 6 in Performance improvement through quality evaluations of sterile cactus moths, Cactoblastis cactorum (Lepidoptera: Pyralidae), mass-reared at two insectaries
Fig. 6. The mean distance (m) from the field release site that Cactoblastis cactorum males were recaptured was significantly influenced by the insectary (DPI or TIF), the day that released males were recaptured, and the trial conducted before (trial 1) and afer (trial 2) quality improvements were made to the rearing and handling protocols at the DPI insectary. Vertical bars denote 0.95 confidence intervals.
Fig. 2 in Performance improvement through quality evaluations of sterile cactus moths, Cactoblastis cactorum (Lepidoptera: Pyralidae), mass-reared at two insectaries
Fig. 2. The mean percentage of Cactoblastis cactorum females that were mated at time of collection from the insectaries (DPI or TIF) and the trial conducted before (trial 1) and afer (trial 2) quality improvements were made to the rearing and handling protocols at the DPI insectary. Vertical bars denote 0.95 confidence intervals.
Fig. 3 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs
Fig. 3. Isotope signatures of the African sugarcane borer, Eldana saccharina. Wild moths developed on sugarcane at Eston, and at Tinely Manor, a 3rd group developed on papyrus at Eston and a 4th group was mass reared on an artificial diet. Error bars are 3 standard deviations of the mean.
Fig. 5 in Performance improvement through quality evaluations of sterile cactus moths, Cactoblastis cactorum (Lepidoptera: Pyralidae), mass-reared at two insectaries
Fig. 5. The relationship between the mean percentage recapture of Cactoblastis cactorum males released in the field as influenced by the day that released males were recaptured. Males recaptured include individuals from both DPI and TIF insectaries. Vertical bars denote 0.95 confidence intervals.
Fig. 2 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs
Fig. 2. Isotope signatures of cactus, a laboratory formulated diet and of cactus moths, Cactoblastis cactorum, reared on these 2 substrates; error bars are 2 standard deviations of the mean.
Fig. 4 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs
Fig. 4. Isotope signature of the light brown apple moth, Epiphyas postvittana (LBAM); error bars are 2 standard deviations of the mean.
Fig. 4 in Performance improvement through quality evaluations of sterile cactus moths, Cactoblastis cactorum (Lepidoptera: Pyralidae), mass-reared at two insectaries
Fig. 4. The mean percentage recapture of Cactoblastis cactorum males released in the field as influenced by the insectary (DPI or TIF) and the trial conducted before (trial 1) and afer (trial 2) quality improvements were made to the rearing and handling protocols at the DPI insectary. Vertical bars denote 0.95 confidence intervals.
Fig. 1 in Ability of sterile males to inhibit female remating in the melon fly Zeugodacus cucurbitae (Diptera: Tephritidae)
Fig. 1. Numbers of rematings observed per cage for females first mated to wild or sterile males at 3 intervals afer the initial mating. Each cage held 10 test females. Symbols represent mean values ± 1 SE; N = 8 in all cases.
Text-fig. 2. Tumidopteris astra sp. nov., macromorphology. a, c: sterile pinna, spec. GIN 4851/340; b, d: holotype GIN 4851/343h; e: sterile pinna, spec. GIN 4851/344. Localities: the city of Vorkuta, Section 49, layer 254 (a, c), the borehole IK-675, depth 961.7 m (b, d), the borehole IK-677, depth 147.8 m (e). Scale 1 cm (a, b, c, e), 1 mm (d). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 2. Tumidopteris astra sp. nov., macromorphology. a, c: sterile pinna, spec. GIN 4851/340; b, d: holotype GIN 4851/343h; e: sterile pinna, spec. GIN 4851/344. Localities: the city of Vorkuta, Section 49, layer 254 (a, c), the borehole IK-675, depth 961.7 m (b, d), the borehole IK-677, depth 147.8 m (e). Scale 1 cm (a, b, c, e), 1 mm (d).
Text-fig. 4. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori (a, b, c), epidermal structure (e) and the sterile pinna (d; spec. 4851/344). a: partly damaged sorus; b: partly damaged sorus with six sporangia; c: two neighboring sori; d: part of the sterile pinna; e: costal epiderma. Scale 500 Μm (a, b, c), 1 cm (d), 200 Μm (e). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 4. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori (a, b, c), epidermal structure (e) and the sterile pinna (d; spec. 4851/344). a: partly damaged sorus; b: partly damaged sorus with six sporangia; c: two neighboring sori; d: part of the sterile pinna; e: costal epiderma. Scale 500 Μm (a, b, c), 1 cm (d), 200 Μm (e).
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.