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Fig. 6 in Repellency of two essential oils to Monomorium pharaonis (Hymenoptera: Formicidae)
Fig. 6. Mean numbers of ants present on DMSO-treated and untreated control filter papers in the absence or presence of food at different hours of observation. Values are means of 6 replications, and bars indicate the standard error. The mean numbers of ants were compared by paired t-tests at a significance level of P ≤ 0.05. No significant differences between DMSO and untreated control were found.
Fig. 4 in Repellency of two essential oils to Monomorium pharaonis (Hymenoptera: Formicidae)
Fig. 4. Mean numbers of ants present on treatment and control filter papers in tests with essential oils at a concentration of 1,000 ppm in the absence or presence of food at different hours of observation. Values are means of 6 replications, and bars indicate the standard error. The mean numbers of ants were compared by paired t-tests at a significance level of P ≤ 0.05. No significant differences between treatment and control were found.
Fig. 5 in Repellency of two essential oils to Monomorium pharaonis (Hymenoptera: Formicidae)
Fig. 5. Mean numbers of ants present on treatment and control filter papers in tests with essential oils at a concentration of 100 ppm in the absence or presence of food at different hours of observation. Values are means of 6 replications, and bars indicate the standard error. The mean numbers of ants were compared by paired t-tests at a significance level of P ≤ 0.05. No significant differences between treatment and control were found.
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 Repellency of two essential oils to Monomorium pharaonis (Hymenoptera: Formicidae)
Fig. 3. Percentage of repellency (PR) of Curcuma longa and Litsea cubeba against Monomorium pharaonis in the absence or presence of food at different hours of observation. Values are means of 6 replications, and bars indicate the standard error. The PR values were analyzed by 1-way ANOVA and Tukey's HSD test at a significance level of P ≤ 0.05. An asterisk indicates a significant difference between absence and presence of food.
Fig. 2 in Repellency of two essential oils to Monomorium pharaonis (Hymenoptera: Formicidae)
Fig. 2. Mean numbers of ants present on treatment and control filter papers in tests with essential oils at a concentration of 10,000 ppm in the absence or presence of food at different hours of observation. Values are means of 6 replications, and bars indicate the standard error. The mean numbers of ants were compared by paired t-tests at a significance level of P ≤ 0.05. An asterisk indicates a significant difference between treatment and control.
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. 1 in Repellency of two essential oils to Monomorium pharaonis (Hymenoptera: Formicidae)
Fig. 1. Experimental setup of the area choice test, with two filter paper half discs fitted in the bottom of a Petri dish. In the "with food" test, food was placed centrally on each half disc.
Fig. 1 in Differences in seasonal variation between two biotypes of Megamelus scutellaris (Hemiptera: Delphacidae), a biological control agent for Eichhornia crassipes (Pontederiaceae) in Florida
Fig. 1. Average number of F1 adults, average weight, and average development time (+ SE) across typical seasonal temperatures in Davie, Florida. An asterisk (*) indicates significance at the α = 0.05 level.
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. 3 in Interspecific competition between two exotic parasitoids (Hymenoptera: Aphelinidae) of an invasive Bemisia tabaci species (Hemiptera: Aleyrodidae)
Fig. 3. Mean (± SE) number of progeny produced by Eretmocerus sp. nr. emiratus under all parasitoid release combinations and host plants. Treatment types are abbreviated as follows: Ee, Er. sp. nr. emiratus only; Eb/Ee, Encarsia bimaculata followed by Er. sp. nr. emiratus; Ee/Eb, Er. sp. nr. emiratus followed by En. bimaculata; Ee+Eb, Er. sp. nr. emiratus and En. bimaculata together. Columns with the same lower case letter within each host plant are not significantly different (difflsmeans, P> 0.05).
Fig. 1 in Interspecific competition between two exotic parasitoids (Hymenoptera: Aphelinidae) of an invasive Bemisia tabaci species (Hemiptera: Aleyrodidae)
Fig. 1. Mean rates of parasitism (% ± SE) under all parasitoid release combinations and host plants. Treatment types are abbreviated as follows: Eb, Encarsia bimaculata only; Eb/Ee, En. bimaculata followed by Eretmocerus sp. nr. emiratus; Ee, Er. sp. nr. emiratus only; Ee/Eb, Er. sp. nr. emiratus followed by En. bimaculata; Ee+Eb, Er. sp. nr. emiratus and En. bimaculata together. Columns with the same lower case letter within each host plant are not significantly different (difflsmeans, P> 0.05).
Fig. 2 in Interspecific competition between two exotic parasitoids (Hymenoptera: Aphelinidae) of an invasive Bemisia tabaci species (Hemiptera: Aleyrodidae)
Fig. 2. Mean (± SE) number of progeny produced by Encarsia bimaculata under all parasitoid release combinations and host plants. Treatment types are abbreviated as follows: Eb, En. bimaculata only; Eb/Ee, En. bimaculata followed by Eretmocerus sp. nr. emiratus; Ee/Eb, Er. sp. nr. emiratus followed by En. bimaculata; Ee+Eb, Er. sp. nr. emiratus and En. bimaculata together. Columns with the same lower case letter within each host plant are not significantly different (difflsmeans, P> 0.05).
Fig. 1. A in A comparison of two insect collection techniques in oiled and non-oiled salt marshes in Louisiana
Fig. 1. A species accumulation curve for both the sweep net (black) and the vacuum (gray) collection techniques. Dotted lines indicate the 95% confidence interval around each curve. Neither curve reached an asymptote.
Fig. 1 in Competing invaders: Performance of two Anguillicola species in Lake Bracciano
Fig. 1. Life cycle of Anguillicola crassus. The basic life cycle (blue arrow) includes eels as final hosts and copepods as intermediate hosts. By integrating additional paratenic hosts (e.g. fish), the life cycle can be extended (white arrow).Source: (Moravec, 2006).
Fig. 2 in Competing invaders: Performance of two Anguillicola species in Lake Bracciano
Fig. 2. Population growth rate. The relationship between the number of adult individuals per host and the days post infection is shown. The lines represent model predictions and the dots represent experimental data.
Fig. 3 in Competing invaders: Performance of two Anguillicola species in Lake Bracciano
Fig. 3. Development to L3 in intermediate host. Days post infection (dpi) until Anguillicola spp. larvae develop into the infective L3 at 20 ̊C. Most A. crassus larvae develop within 17 dpi while the majority of A. novaezelandiae larvae need 23 dpi to complete the development in the intermediate host.
Fig. 2 in Relative competence of native and exotic fish hosts for two generalist native trematodes
Fig. 2. Mean worm size of the trematodes Telogaster opisthorchis (a) and Stegodexamene anguillae (b) in experimentally infected exotic brown trout and rainbow trout, and native longfin eel. Error bars indicate standard error.
Fig. 3 in Relative competence of native and exotic fish hosts for two generalist native trematodes
Fig. 3. Flowchart summarising the circulation and transmission dynamics of trematodes, (a) Telogaster opisthorchis and (b) Stegodexamene anguillae, in native and exotic hosts in Lake Pearson. (Native fish images; McDowall, 2000; exotic fish; Rauque et al., 2003.)
Fig. 3 in Haemogregarine infections of three species of aquatic freshwater turtles from two sites in Costa Rica
Fig. 3. (A) Average haemogregarine parasitemias (±SD) between black river turtles, Rhinoclemmys funerea, collected from creek and pond sites. (B) Average haemogregarine parasitemias (±SD) of black river turtles, Rhinoclemmys funerea, and white-lipped mud turtles, Kinosternon leucostomum, were significantly different (p = 0.032).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.