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Fig. 2 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 2. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in corn. Weevils were reared on corn, barley, brown rice, and white rice, then presented with a choice of 4 host grains. Means with the same letter are not significantly different.
Fig. 2 in The role of visual organs in the locomotor behavior of Bactrocera minax (Diptera: Tephritidae)
Fig. 2. Schematic diagrams of experimental chambers. A. Take-off platform; B. Horizontal crawling device; C. Vertical crawling device; a. take-off platform; b. Plexiglass box; c. video camera; d. Petri dish; e. crawling column; f. ruler.
Fig. 1 in The role of visual organs in the locomotor behavior of Bactrocera minax (Diptera: Tephritidae)
Fig. 1. Schematic diagram of visual blinding treatments on adult Chinese citrus flies, Bactrocera minax. The white arrow indicates the blinded visual organ.
Fig. 1 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 1. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice. Weevils were reared on corn, barley, brown rice, and white rice, then presented with a choice of 4 host grains. Means with the same letter are not significantly different.
Fig. 4 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 4. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in white rice. Means with the same letter are not significantly different.
Fig. 5 in The role of visual organs in the locomotor behavior of Bactrocera minax (Diptera: Tephritidae)
Fig. 5. Vertical crawling distance (cm in 30 s) of adult Chinese citrus flies, Bactrocera minax, males and females tested separately with 6 visual blinding treatments. Values are mean ± standard error. Histograms with different lowercase letters indicate significant difference among treatments (P <0.05).
Fig. 2. A in Behavior and feeding of two beetle pollinators of Zamia integrifolia (Cycadales): Rhopalotria slossoni (Coleoptera: Belidae) and Pharaxanotha floridana (Coleoptera: Erotylidae)
Fig. 2. A) Pharaxanotha floridana spend more time on the ovulate cone scale than control (p = 0.035) and equal amounts of time on pollen and ovulate cone scales in 30 mins no-choice behavior trials. B) No visible evidence of feeding damage on ovulate cone scale parenchyma tissue, nor on ovules afer 24 h. C) No visible feeding damage on pollen cone scale parenchyma tissue afer 24 h. D) Pharaxanotha floridana E) More mass (mg) is consumed per surviving beetle from ovulate cone scales than from pollen cone scales over 24 h (p = 0.0033). In A and E, summary boxplots are shown with raw data values overlaid.
Fig. 1. A in Behavior and feeding of two beetle pollinators of Zamia integrifolia (Cycadales): Rhopalotria slossoni (Coleoptera: Belidae) and Pharaxanotha floridana (Coleoptera: Erotylidae)
Fig. 1. A) Rhopalotria slossoni spend more time on pollen cone scales than ovulate cone scales (p = 0.041) in 30 mins no-choice behavior trials but show no statistical difference between ovulate and control. B) Ovulate cone scales show extensive feeding damage on their parenchyma tissue afer 24 h. C) Pollen cone scales show feeding damage on the parenchyma tissue afer 24 h. D) Rhopalotria slossoni E) The mass (mg) of tissue consumed per surviving weevil is equal between pollen and ovulate cone scales. In A and E, summary boxplots are shown with raw data values overlaid.
Fig. 1 in Predatory behaviors: Pristimantis savagei (Anura: Craugastoridae) as prey of Trechalea sp. spiders (Araneae: Trechaleidae) in a sector of the Piedemonte Llanero, Villavicencio, Colombia
Fig. 1. Site of Pristimantis savagei predation by Trechalea sp., in a sector of Piedemonte Villavicencio-Meta, Colombia. The red dot indicates the exact site of discovery in the Caño Buque.
Fig. 2 in Predatory behaviors: Pristimantis savagei (Anura: Craugastoridae) as prey of Trechalea sp. spiders (Araneae: Trechaleidae) in a sector of the Piedemonte Llanero, Villavicencio, Colombia
Fig. 2. Record of predation of Pristimantis savagei by Trechalea sp., in a sector of Piedemonte, Villavicencio-Meta, Colombia.
Fig. 3 in Predatory behaviors: Pristimantis savagei (Anura: Craugastoridae) as prey of Trechalea sp. spiders (Araneae: Trechaleidae) in a sector of the Piedemonte Llanero, Villavicencio, Colombia
Fig. 3. Warning stance of the spider Trechalea sp. The individual was on a rock at an approximate height of 150 cm, less than 1 m from the water source.
Fig. 1 in The effects of laboratory rearing diet on recruitment behavior of Wasmannia auropunctata (Hymenoptera: Formicidaea)
Fig. 1. Mean ± SE difference in recruitment rates of laboratory raised Wasmannia auropunctata to non-toxic baits: Hawaii Ant Lab gel bait, 50% gelled sucrose solution, and tuna between pre- and post-treatment measurements of the multi-choice laboratory experiment (n = 5 colonies). Bars in each group with different letters above have statistically different means (P <0.05). Colonies were exposed to their respective dietary treatment (buffet plus crickets: n=5, vegetable oil wick plus crickets: n=5, 25% sucrose solution plus crickets: n=5, and pureed tuna plus crickets: n=5) for 49 d. Means represented in this chart are based on raw data for visualization and are not the reported marginal means.
Fig. 2 in The effects of laboratory rearing diet on recruitment behavior of Wasmannia auropunctata (Hymenoptera: Formicidaea)
Fig. 2. Recruitment rates (mean number of ants ± SE) of wild Wasmannia auropunctata to the Hawaii Ant Lab gel bait, 50% gelled sucrose solution, and tuna for multi-choice (n = 6 per treatment) and no-choice (n = 6 per treatment) field experiments. Bars within clusters with different letters above have statistically different means (P <0.05). Means represented in this chart are based on raw data for visualization and not proportional results from the Poisson distributed generalized linear mixed model as reported.
Figs 2-6. Agonistic behavior between a in The hard task of a short-tailed mouse opossum (Monodelphis) to prey a harvestman (Arachnida: Opiliones)
Figs 2-6. Agonistic behavior between a harvestman of the family Gonyleptidae and the mouse opossum Monodelphis dimidiata (Wagner, 1847). The interaction starts with the mouse opossum in an attack position, facing the harvestman (Fig. 2), then the marsupial staggers side to side (Fig. 3) and is knocked out (Fig. 4). This sequence of events is repeated two times, until the mouse opossum assumes its third attack position and attacks the harvestman (Fig. 5). The mouse opossum removes the harvestman's legs one by one to then feed on its body (Fig. 6). Image edited in the Inkscape software.
Figs 7–18 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 7–18. Immature stages of Nisoniades macarius (Herrich-SchÄffer, 1870) in dorsal (left) and lateral (right) views: 7, 8, first instar larva; 9, 10, second instar larva; 11, 12, third instar larva; 13, 14, fourth instar larva; 15, 16, fifth instar larva; 17, 18, sixth instar larva.
Figs 28–31 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 28–31. TYpes of shelters built bY the larva of Nisoniades macarius (Herrich-SchÄffer, 1870) in Ipomoea asarifolia (Desr.) Roem. & Schult: 28, 29, TYpe 3 shelter, or center-cut shelters; 30, 31, TYpe 5 shelter, or two-cut shelters. The red arrows point to the shelter's location.
Figs 1, 2 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 1, 2. Collection area of the immatures of Nisoniades macarius (HerrichSchÄffer, 1870) (Fig. 1); the host plant of N. macarius, Ipomoea asarifolia (Desr.) Roem. & Schult. (Fig. 2).
Figs 32–36 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 32–36. Parasitoid of Nisoniades macarius (Herrich-SchÄffer, 1870) larva: 32, parasitized first instar larva; 33, parasitized third instar larva. Pupa of the parasitoid: 34, ventral view; 35, dorsal view. Fig. 36, parasitoid in adult form. The red arrows point to the parasitoid larvae.
Figs 3–6 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 3–6. Egg of Nisoniades macarius (Herrich-SchÄffer, 1870): 3, egg in the adaxial portion of the Ipomoea asarifolia (Desr.) Roem. & Schult. leaf; 4, egg in dorsal view; 5, egg in lateral view close to hatching; 6, egg after hatching.
Figs 19–27 in Immature stages of Nisoniades macarius (Hesperiidae: Pyrginae: Carcharodini): biology, morphology and behavior
Figs 19–27. Immatures and adults of Nisoniades macarius (Herrich-SchÄffer, 1870). Pre-pupa: 19, dorsal view; 20, lateral view. Pupa: 21, dorsal view; 22, lateral view; 23, ventral view; 24, frontal view. Fig. 25, adult female resting on grass leaf close to the host plant. Dorsal (left) and ventral (right) views of the adults raised in the laboratorY: 26, female; 27, male.
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.