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77 results for “environmental behaviors”
Data from: A dynamic state model of migratory behavior and physiology to assess the consequences of environmental variation and anthropogenic disturbance on marine vertebrates
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Data from: Butterfly density and behaviour in uncut hay meadow strips: behavioral ecological consequences of an agri-environmental scheme
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Fig. 6 in Silk Spinning Behavior Varies from Species-Specific to Individualistic in Embioptera: Do Environmental Correlates Account for this Diversity?
Fig. 6. Multidimensional scaling plot of sequence similarity (n = 15). Each individual is plotted with its species code, and six species are highlighted in color. Those in shades of blue showed particularly low intraspecific similarity, while those in warm shades showed high intraspecific similarity. (A) Low temperature seasonality (<2000), (B) Moderate temperature seasonality (2000–4000), (C) High temperature seasonality (>4000). Legend shows species names and abbreviations.
Fig. 2 in Silk Spinning Behavior Varies from Species-Specific to Individualistic in Embioptera: Do Environmental Correlates Account for this Diversity?
Fig. 2. Examples of silk spun by embiopterans in their natural habitats. Domicile and gallery structure scores used in the statistical analyses are reported in SuppTable 2 [online only]. (A) Clothoda nr. longicauda Ross (Clothodidae) with exposed silk typified by a thick outer coating of silk, in this case reinforced even further with gathered materials, (B) Pararhagadochir trinitatis (Saussure) (Scelembiidae) with galleries exposed to the elements but quite thin, (C) Conicercembia septentrionalis (Mariño & Márquez) (Scelembiidae) with very thin exposed silk over the bark, (D) Notoligotoma hardyi (Friederichs) (Notoligotomidae) showing a typical colony on lichen-covered granite with a close-up of the exposed thick tubes of silk, (E) Neorhagadochir moreliensis (Ross) (Scelembiidae) with thick silk tubes found under bark flaps, (F) Ptilocerembia thaidina Poolprasert & Edgerly (Ptilocerembiidae) with very thin silk, also found mostly living under bark and inside crevices, (G and H) Metoligotoma species Davis (Australembiidae) all of which live in leaf litter; (I) Haploembia tarsalis (Ross) (Oligotomidae) with thin silk lining underground crevices, (J) Haploembia solieri with thin silk under rocks and in leaf litter.
Fig. 1 in Silk Spinning Behavior Varies from Species-Specific to Individualistic in Embioptera: Do Environmental Correlates Account for this Diversity?
Fig. 1. Adult Embioptera illustrating morphological uniformity of females and typical male traits. (A) Female Eosembia auripecta Ross (Oligotomidae), (B) Female Antipaluria urichi (Saussure) (Clothodidae), (C) Female Metoligotoma pentanesiana Davis (Australembiidae), (D) Male and female Aposthonia ceylonica (Enderlein) (Oligotomidae), (E) Haploembia solieri (Rambur) (Oligotomidae) male.
Data from: Using artificial intelligence classification of videos to examine the environmental, evolutionary and physiological constraints on provisioning behavior
<p>The use of artificial intelligence (AI) technologies can revolutionize how we approach data collection and analysis in behavioral ecology. One such example is in provisioning behavior. Parents of altricial species are selected to provide parental care (such as food provisioning) for their offspring, but there is substantial variation in the level of this care. Provisioning rate may be determined environmentally, by the physiological ability of parents and needs of nestlings, or by evolutionary incentives. We quantified provisioning rate in 20 purple martin (<i>Progne subis</i>) nests in the context of an experimental reduction of nest ectoparasites. 10 nests had a parasite reduction treatment, and 10 nests were controls. By using AI to automate the analysis of nest camera videos we were able to obtain nearly-continuous provisioning rate information at a high temporal resolution for the first half of the nestling period. We used random forest modeling to assess the factors determining provisioning rate and found evidence for environmental, evolutionary and physiological constraints and incentives on provisioning. Birds appeared to be environmentally limited in their provisioning in cool, wet conditions, especially later in the breeding season; but adjusted their provisioning according to the changing physiological needs of nestlings. We found evidence for a compensatory response to increased parasite load, in which parents increased provisioning to more heavily parasitized nests.</p>
Data from: A test for environmental effects on behavioral isolation in two species of killifish
Behavioral isolation is a common and potent mechanism of reproductive isolation. Determining the extent to which behavioral isolation varies with environmental conditions is critical to understanding speciation and the maintenance of species boundaries. Here, we tested the effect of salinity on behavioral isolation (female species recognition, male-male competition, male species recognition) between two closely related killifish (Lucania goodei and L. parva) that differ in salinity tolerance. We performed no-choice assays and behavioral trials where males could compete and court females in fresh water (0 ppt) and brackish water (15 ppt). We found high levels of behavioral isolation that did not vary as a function of salinity. In behavioral trials, male species recognition of females was strong and asymmetric between the two species. Lucania goodei males preferred conspecifics and rarely courted or mated with L. parva females. Lucania parva males preferred conspecifics but readily courted and mated with L. goodei females. This asymmetry matches previously documented asymmetries in hybrid offspring fitness. Crosses between L. parva males and L. goodei females produce fully viable/fertile hybrids, but crosses between L. goodei males and L. parva females produce males with reduced fertility. Hence, behavioral isolation may have evolved in part due to reinforcement.
Differential impacts of environmental yeasts on larval development and oviposition behavior of the Asian tiger mosquito Aedes albopictus
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Crafting Green Destinations: The Impact of Social Media and Community Engagement on Environmental Behaviors in Tourist Hotspots
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Environmental and Behavioral Risk Factors for Childhood Drowning
ClinicalTrials.gov study NCT00341289. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Environmental Design for Behavioral Regulation in People With Dementia
ClinicalTrials.gov study NCT04555616. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: The influence of environmental variance on the evolution of signalling behavior
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Data from: A test for environmental effects on behavioral isolation in two species of killifish
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Data from: Environmental sources of bacteria and genetic variation in behavior influence host-associated microbiota
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Data from: Modeling the effect of environmental temperatures, microhabitat, and behavioral thermoregulation on predicted activity patterns in a desert lizard across its thermally diverse distribution
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Data from: Using artificial intelligence classification of videos to examine the environmental, evolutionary and physiological constraints on provisioning behavior
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Environmental and simulation facility conditions can modulate a behavioral-driven altered gravity response of Drosophila imagoes transcriptome
Genome-wide transcriptional profiling shows that reducing gravity levels in the International Space Station (ISS) causes important alterations in Drosophila gene expression. However simulation experiments on ground without space constraints show weaker effects than space environment. A global and integrative analysis using the gene expression dynamics inspector (GEDI) self-organizing maps reveals a subtle response of the transcriptome using different populations and microgravity and hypergravity simulation devices. These results suggest that in addition to behavioural responses that can be detected also at the gene expression level the transcriptome is finely tuned to normal gravity. The alteration of this constant parameter on Earth can have effects on gene expression that depends both on the environmental conditions and the ground based facility used to compensate the gravity vector. Alternative and commons effects of mechanical facilities like the Random Positioning Machine and a centrifuge and strong magnetic field ones like a cryogenically cooled superconductive magnet are discussed. We compare the effects over the gene expression profile of different gender/age Drosophila imagoes in 3-4 days-long experiments under altered gravity conditions into three GBF (Ground Based Facilities for micro/hyper- gravity simulation) using whole genome microarray platforms. Descriptions of different GBFs (treatments): LDC means Large Diameter Centrifuge. Samples can be placed under three conditions: inside LDC (at certain g level) at the LDC rotational control and at external 1g control (outside the LDC). RPM means Random Positioning Machine. Samples can be placed under two conditions: inside RPM (at nearly 0g Microgravity level) and at external 1g control (outside the RPM). At the magnet means INSIDE the Magnetic levitator (another GBF). Samples can be placed under four conditions: inside Magnet 0g* (at microgravity with magnetic field) inside Magnet at 1g* (internal control with magnetic field) or inside the magnet 2g* (at hypergravity with magnetic field) and at external 1g control (outside the magnet)
Early-life environmental enrichment generates persistent individualized behavior in mice
GEO Series GSE139051. Mus musculus. 15 samples. Type: Methylation profiling by high throughput sequencing.
An Investigation into the Mechanisms of Media Use Influencing Pro-environmental Contextual Forces and Sustainable Behaviors in Rural Tourism
<p><strong>An Investigation into the Mechanisms of Media Use Influencing Pro-environmental Contextual Forces and Sustainable Behaviors in Rural Tourism</strong></p>
Social-environmental, Psychosocial, Behavioral, Clinical and Biological Drivers of Disparities in Liver Disease Progression Among Korean American With Chronic Hepatitis B Infection
ClinicalTrials.gov study NCT05117541. IPD Sharing: Not stated. Countries: 1. Publications: 0.
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.