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172 results for “Feeding behavior”
Growth, Dietary Intakes and Feeding Behaviors of Children With Cerebral Palsy Who Have Chewing Disorders
ClinicalTrials.gov study NCT02777645. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
The Effect of Time-Restricted Feeding on Anthropometry, Biochemical Parameters, Diet Quality and Eating Behavior
ClinicalTrials.gov study NCT05756868. IPD Sharing: YES. Countries: 1. Publications: 0.
Impact of Behavioral Feeding Intervention on Parent-Child Attachment in Young Children
ClinicalTrials.gov study NCT02187952. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Neural, Behavioral and Physiological Correlates of Feeding in Humans
ClinicalTrials.gov study NCT01665560. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Dietary zinc status reversibly alters both the feeding behaviors of the rats and gene expression patterns in diencephalon
GEO Series GSE31430. Rattus norvegicus. 16 samples. Type: Expression profiling by array.
microRNA-33 controls feeding behavior by activating hypothalamic AgRP neurons
GEO Series GSE222191. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
FIGURE 4 in Maximum Bite Force and Prey Size of Tyrannosaurus rex and Their Relationships to the Inference of Feeding Behavior
FIGURE 4 Relationship between bite force and body mass in predatory amniotes. This relationship was analyzed in order to infer the likely maximum bite force of the theropod dinosaur Tyrannosaurus rex. Bite force data obtained from extant predatory crocodylians, chelonians, squamates, and mammals are plotted against their body masses (see Table I) and subjected to correlation and least squares regression analyses. The bite forces of these predators are strongly correlated with their body masses across clades (r = 0.939; r2 = 0.882) and bite force increases with significant positive allometry relative to body mass (see text). Extrapolation of the regression to the estimated body mass of T. rex makes it possible to estimate its bite force at 235,000 N. Allometric increase in bite force is required only if selection continues to favor feeding on absolutely larger prey. If T. rex was not a direct, active predator of adult ornithischian dinosaurs of comparable size, its bite force should be lower than that predicted at its large body size, based upon data from extant predators.
FIGURE 5 in Maximum Bite Force and Prey Size of Tyrannosaurus rex and Their Relationships to the Inference of Feeding Behavior
FIGURE 5 Relationship between body mass of largest known prey (mean value) and the body mass of its predator (species mean). Considerable variability in this relationship is partly attributable to differences in predatory behavior. Pack hunting, for example, allows a predator to take relatively large prey. The relationship between Triceratops horridus and Tyrannosaurus rex falls well within the range extrapolated from data for extant (mammalian) carnivores and their prey. This indicates that T. rex could have been a competent predator of adult Triceratops horridus, even if acted as a solitary predator. Social groups of other large theropods may have been capable of dispatching significantly larger prey species, possibly even including adult sauropods.
Fig. 12. Phylogenetic hypotheses for the stenine group. A in Larval Description, Adult Feeding Behavior, and Phylogenetic Placement of Megalopinus (Coleoptera: Staphylinidae)
Fig. 12. Phylogenetic hypotheses for the stenine group. A) Consensus tree based on adult characters with bootstrap values. B) Consensus tree based on larval characters with bootstrap values. C) Cladogram based on combined data with Bremer and bootstrap values.
Fig. 8 in Feeding, Reproductive, and Nesting Behavior ofCanthon bispinusGermar (Coleoptera: Scarabaeidae: Scarabaeinae)
Fig. 8. Brood balls of Canthon bispinus. A) Shaped as a figure eight, B) Shaped as a pear, C) Internal view showing an egg in the chamber, D) Aspect after emergence of the imago emergence, showing the larval excreta outside. Scale bars = 5 mm.
fish feeding behavior dataset
Open the record for dataset details and reuse information.
Feeding behavioral order data
<p>Raw feeding behavioural data output from BORIS in .csv format.</p>
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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.