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Fig. 3 in The effect of environmental enrichment on Salvator merianae (Squamata: Teiidae) under captivity conditions
Fig. 3. Comparison in the frequency of Reproductive Behavior in Males between R1 and R2 during the 3 months of the experiment. Fig. 3. Comparación en la frecuencia del Comportamiento Reproductivo en Machos entre R1 y R2 durante los 3 meses del experimento.
Fig. 2 in The effect of environmental enrichment on Salvator merianae (Squamata: Teiidae) under captivity conditions
Fig. 2. Comparison of cumulative proportions of behavioral categories in R1 and R2, with and without enrichment (inner circle: females, outer circle: males). Fig. 2. Comparación de proporciones acumuladas de categorías de comportamiento en R1 y R2, con y sin enriquecimiento (círculo interior: mujeres, círculo exterior: hombres).
Fig. 4 in The effect of environmental enrichment on Salvator merianae (Squamata: Teiidae) under captivity conditions
Fig. 4. Tables of sociometric matrices for each enclosure R1 and R2, with (R2 WE) and without enrichment (R2 W/O-E). MWM: male without mark, MWP: male white point, MYP; male yellow point, F: female. Fig. 4. Cuadros de matrices sociométricas para cada recinto R1 y R2, con (R2 WE) y sin enriquecimiento (R2 W/O-E). MWM: macho sin marca, MWP: macho punto blanco, MYP; punto amarillo macho, F: hembra.
Fig. 1 C-D in Preliminary larvicidal effect of seed oil from Cleome arabica L. on fifth instar larvae of Schistocerca gregaria (Orthoptera: Acrididae)
Fig. 1 C-D. Cleome arabica at fruiting stage (Oued Metlili, Region of Ghardaïa-Northern Algerian Sahara, April 2020). C) Fruiting brunches. D) Fruiting close-up.
Fig. 1 A-B in Preliminary larvicidal effect of seed oil from Cleome arabica L. on fifth instar larvae of Schistocerca gregaria (Orthoptera: Acrididae)
Fig. 1 A-B. Cleome arabica at fruiting stage (Oued Metlili, Region of Ghardaïa-Northern Algerian Sahara, April 2020). A) Whole plant. B) Seed.
Fig. 1 in The effect of environmental enrichment on Salvator merianae (Squamata: Teiidae) under captivity conditions
Fig. 1. Examples of different environmental enrichment activities carried out in the R2. Fig. 1. Ejemplos de diferentes actividades de enriquecimiento ambiental realizadas en el R2.
Fig. 5 A-B in Preliminary larvicidal effect of seed oil from Cleome arabica L. on fifth instar larvae of Schistocerca gregaria (Orthoptera: Acrididae)
Fig. 5 A-B. Morphological abnormalities observed in L5 muer larvae of S. gregaria treated with C. arabica seed oil.
Fig. 4 A-B. Dead L5 in Preliminary larvicidal effect of seed oil from Cleome arabica L. on fifth instar larvae of Schistocerca gregaria (Orthoptera: Acrididae)
Fig. 4 A-B. Dead L5 larvae following the inability to molt observed in S. gregaria L5 treated with C. arabica seed oil.
Figure 4 in Survival of entomopathogenic nematodes in oil emulsions and control effectiveness on adult engorged ticks (Acari: Ixodida)
Figure 4: Effectivity of EPNs at concentration of 100 IJs/tick in vegetable oil emulsions at concentration of 33% on engorged adult ticks. Bars with unequal letters are statistically different (Tukey, P <0.05).
Figure 2 in Survival of entomopathogenic nematodes in oil emulsions and control effectiveness on adult engorged ticks (Acari: Ixodida)
Figure 2: Survival of EPNs in oil emulsions of J. VirGiniana and C. CitratUS at a concentration of 13% under laboratory conditions.
Figure 3 in Survival of entomopathogenic nematodes in oil emulsions and control effectiveness on adult engorged ticks (Acari: Ixodida)
Figure 3: Effectivity of EPNs at concentration of 50 IJs/tick in vegetable oil emulsions at concentration of 33% on engorged adult ticks. Bars with unequal letters are statistically different (Tukey, P <0.05).
Figure 5 in Survival of entomopathogenic nematodes in oil emulsions and control effectiveness on adult engorged ticks (Acari: Ixodida)
Figure 5: Control effectiveness of S. websteri at 119 IJs/tick in two vegetable oil emulsions at a concentration of 33% and a Control with S. websteri in only distilled water.
Figure 6 in Fitness Effects of Founder Female Number of Trichogramma papilionis Reared on Ephestia kuehniella
Figure 6. Coefficient of variation in percentage parasitized Ephestia eggs for three different founder population size colonies (Treatments, 1, 2, and 10 founder females) of Trichogramma papilionis over 10 successive generations.
Figure 4 in Fitness Effects of Founder Female Number of Trichogramma papilionis Reared on Ephestia kuehniella
Figure 4. Mean estimates (± SEM) of the sex ratio of Trichogramma papilionis in two experimental lines (25°C, L1 and 22°C, L2). Treatments not connected by the same letter were significantly different.
Figure 1 in Fitness Effects of Founder Female Number of Trichogramma papilionis Reared on Ephestia kuehniella
Figure 1. Response (Mean ± SEM) in the emergence rate of three founder population sizes (1, 2, and 10 founder females) of Trichogramma papilionis over 10 serially bottlenecked generations. Treatments not connected by the same letter were significantly different (Tukey test, P <0.050).
Figure 2 in Fitness Effects of Founder Female Number of Trichogramma papilionis Reared on Ephestia kuehniella
Figure 2. Coefficient of variation in the emergence rate of Trichogramma papilionis from three founder population sizes (Treatments, 1, 2, 10 females) over ten generations.
Figure 1 in Effect of Pupal Holding Density on Emergence Rate, Flight Ability, and Yield of Sterile Male Mediterranean Fruit Flies (Diptera: Tephritidae)
Figure 1. Emergence rate (top) and flight ability (bottom) for Hawaii- and Guatemaladerived flies when held at loadings of 250, 350, or 450 ml per eclosion tower tray. Bar heights represent mean values over all trays for a given density (15 dates X 6 trays per loading amount per date = 90 trays total), and error bars represent 1 SE.
Figure 2 in Mark-Release-Recapture Experiments on the Effectiveness of Methyl Eugenol-Spinosad Male Annihilation Technique Against an Invading Population of Bactrocera dorsalis
Figure 2. Visual representation of the MAT-ME saturation hypothesis. Darker areas represent higher concentrations of attractant odor in the air column, represented from above. (A) A single sentinel trap baited with 6 ml of methyl eugenol under control conditions. A release of males around the center of the area would lead some of the males to find the plume and successfully follow it to the trap for capture. (B) A single sentinel trap with some MAT-ME spots (low rate). More attractant is available, but gradients to point sources are still clear; note that the MAT-ME spots have a lower overall concentration at the source. (C) A single sentinel trap with a high density of MAT-ME spots. A haze of attractant exists, making gradients shorter. The sentinel trap is still about as effective as before due to higher final concentration, but the less concentrated MAT-ME spots are harder to find.
Figure 1 in Mark-Release-Recapture Experiments on the Effectiveness of Methyl Eugenol-Spinosad Male Annihilation Technique Against an Invading Population of Bactrocera dorsalis
Figure 1. Mean proportion recaptured by treatment. Whiskers indicate standard errors. Letters indicate statistically significant differences at α = 0.05 via two-sample z-test (see text for details)
Figure 1 in Effect of the Guppy, Poecilia reticulata, on Oviposition of Culex quinquefasciatus (Diptera: Culicidae)
Figure 1. (A) Average numbers (±SE) of egg rafts laid by Culex quinquefasciatus in treatment (with one mosquito fish) and control (without mosquito fish), and (B) average per night (±SE) of gravid Culex quinquefasciatus females collected in gravid traps (treatment: 10 mosquito fish; control: without mosquito fish). Both vertical bars represent standard error.
ScienceDex guides
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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.