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240 results for “social interaction”
Sex- and social context-dependent differences in mice head movement during social interactions
<p>Data set and code for the paper : <span>S<span>ex- and social context-dependent differences in mice head movement during social interactions. </span></span></p> <p><span>Adèle Phalip<sup>1,</sup>*, Shai Netser<sup>1</sup> and Shlomo Wagner<sup>1</sup></span></p> <p><span> </span></p> <p><sup><span>1</span></sup><span>Sagol Department of Neurobiology, Faculty of Natural Sciences, University of Haifa, Haifa, Israel</span></p> <p><span> </span></p> <p><span><span><span>*Corresponding author: </span><span><a href="mailto:adele.phalip@gmail.com"><span>adele.phalip@gmail.com</span></a></span></span></span></p>
Supplementary material 3 from: Schmidt K, Walz A (2021) Ecosystem-based adaptation to climate change through residential urban green structures: co-benefits to thermal comfort, biodiversity, carbon storage and social interaction. One Ecosystem 6: e65706. https://doi.org/10.3897/oneeco.6.e65706
Mean values of microclimatic parameters between 9am and 9pm, based on measurements in the four courtyards (CY): CY 1: light green, CY 2: dark green, CY 3: orange, CY 4: red
Supplementary material 6 from: Schmidt K, Walz A (2021) Ecosystem-based adaptation to climate change through residential urban green structures: co-benefits to thermal comfort, biodiversity, carbon storage and social interaction. One Ecosystem 6: e65706. https://doi.org/10.3897/oneeco.6.e65706
Results from tree mapping and allometric equations, indicating above-ground biomass and carbon stocks
Supplementary material 5 from: Schmidt K, Walz A (2021) Ecosystem-based adaptation to climate change through residential urban green structures: co-benefits to thermal comfort, biodiversity, carbon storage and social interaction. One Ecosystem 6: e65706. https://doi.org/10.3897/oneeco.6.e65706
Results from habitat mapping and biodiversity scores. Domin values = 1: < 4% cover with few individuals; 2: < 4% with several individuals; 3: < 4% with many individuals; 4: 4–10%; 5: 11–25%; 6: 26–33%; 7: 34–50%; 8: 51–75%; 9: 76–90%; 10: 91–100% cover
Kinematic analysis of social interactions deconstructs the evolved loss of schooling behavior in cavefish
<p>Video tracking software (<a href="https://zenodo.org/api/files/cfb2f8f7-ecb0-4ef8-a16c-3f50e620549c/trilab-tracker-0.2.0.zip?versionId=ec71e34e-8049-450e-b00e-102d67cc3a43">trilab-tracker-0.2.0.zip</a>) and dataset (<a href="https://zenodo.org/api/files/cfb2f8f7-ecb0-4ef8-a16c-3f50e620549c/dataset.zip?versionId=025b9b87-2b06-4012-adb3-cd1b508d5bd1">dataset.zip</a>) for the research article "Kinematic analysis of social interactions deconstructs the evolved loss of schooling behavior in cavefish". The latest version of Trilab-Tracker can be found at <a href="https://github.com/yffily/trilab-tracker">https://github.com/yffily/trilab-tracker</a>.</p>
Data from: Not just females: the socio-ecology of social interactions between spider monkey males
<p class="MsoNormal"><span>Male-male relationships are mostly characterized by competition. However, males also cooperate with one another if socio-ecological conditions are suitable. Due to their male philopatry, need for cooperation in home range defence and high degree of fission-fusion dynamics, spider monkeys provide an opportunity to investigate how male-male interactions are associated with socio-ecological factors, such as the presence of potentially receptive females, the degree of food availability and the likelihood of home range defence. We tested predictions about changes in social interactions between wild spider monkey males in relation to these factors. First, males did not change their interaction patterns when potentially receptive females were in the subgroup compared to when they were absent. Second, males tended to be less tolerant of one another when feeding, but spent more time grooming, in contact and proximity with one another when food availability was lower than when it was higher. Third, males exchanged fewer embraces, spent less time grooming, in proximity and in contact with one another, and spent more time vigilant at the home range boundary area than at other locations. Our findings contribute to the understanding of social flexibility and the importance of considering males in socio-ecological models of any group-living species.</span></p>
Github Repository for "Social interactions generate complex selection patterns in virtual worlds"
<p>Repository for <br><strong>"Social interactions generate complex selection patterns in virtual worlds"</strong><br><em>Francesca Santostefano, Maxime Fraser Franco, Pierre Olivier Montiglio</em><br>Journal of Evolutionary Biology 2024</p>
Dataset Cntnap2 - Free social interaction
<p>We collected electrophysiology data from EAr implanted KO and C57 mice which are added here. We further analyzed this raw data using DeepPhenotyping codes shared in 10.5281/zenodo.10232645 . The DLC and SIMBA models, used to annotate social behavior, have been added to this repository.</p>
The Conversationality Index: A quantitative assessment of conversation in social media interactions - Supplementary Material
<p>Supplementary Material for "The Conversationality Index: A quantitative assessment of conversation in social media interactions". The data contain transcripts of 12 online conversations (Dataset S1) and a table (Table 1A) showing a breakdown of the Conversationality Index scores for the conversations.</p>
Dataset 2 for paper - Distinct prelimbic cortex neuronal responses drive emotion recognition in male mice during Social Interactions-Behavior - Behavior, Piezo, FP and optogenetics datasets
<p>The uploaded folders contain data for:</p> <p>1) Analyzed video clips for behavioral testing of C57BL/6J ESP data for both males and females in ESPr, ESPs, ESPi, and ESPi with female subject and male stimuli, and the Three Discrimination Task. Relevant for Figure.1 and Supp.1.</p> <p>2) Piezo data for ESPs with males, ESPi with males, and ESPi with females. Relevant for Fig.2 Each task folder contains 3 subfolders:</p> <p> 1- Timestamps</p> <p> 2- Piezo-sensors signal</p> <p> 3- Analyzed videos</p> <p>2) Fiber Photometry data for the SP, ESPs, ESPi, and Food vs. Object tasks. Relevant for Fig.3-4 and Supp.2-8. The data for each task is divided into 3 folders:</p> <p> 1- Timestamps</p> <p> 2- Fiber photometry signal</p> <p> 3- Analyzed videos</p> <p>3) Optogenetics data for SP, ESPs (excitation and inhibition), and stimulation with Empty Chambers. Relevant for Fig.8 and Supp.16. The SP and ESPs tasks in this experiment have 4 conditions, and the stimulation with empty chambers test has only the first 3 conditions of the following:</p> <p> 1- No stimulation</p> <p> 2- Stimulation with stimulus 1</p> <p> 3- Stimulation with stimulus 2</p> <p> 4- Free stimulation</p> <p>Data folders for conditions 2 and 3 contain two sub-folders:</p> <p> 1- Timestamps for the delivered optic stimulations</p> <p> 2- Analyzed videos</p>
Dataset Leveraging Social Media Marketing to Enhance Purchase Intention: The Role of Parasocial Interaction and Brand Equity in Green Fashion
<p>The following dataset is a dataset from a study that investigated social media marketing activities that affect parasocial interaction and brand equity. In addition, this study also aims to investigate the relationship of parasocial interaction and brand equity to purchase intention.</p>
Data from: Use of a rostral appendage during social interactions in the Ecuadorian Anolis proboscis
The use of sexually selected characters in inter- and intra-sexual interactions has long been of interest to evolutionary biologists. Recently, a distinction between sexually selected traits as ornaments versus weapons has been advanced. We investigated the behaviour of an enigmatic lizard with a prominent sexually dimorphic trait in an effort to describe whether the trait was the product of sexual selection and further whether it functioned as a weapon or an ornament. The subject of our study was the Ecuadorian proboscis anole (Anolis proboscis), a slow-moving cryptic species endemic to the north-western slopes of the Andes in Ecuador. Males, but not females, of this species bear a rostral appendage that has been described as an exaggerated trait resulting from sexual selection. However, a thorough description of the use of the rostral appendage in social interactions is lacking. Here, we describe social interactions of this species during 11 male–female courtships and mating interactions, as well as three male–male agonistic interactions. We describe four types of displays by males, many involving the rostral appendage. We found that the rostral appendage is used as an ornament in social displays but not as a weapon in combat. We also show that, unlike other lizards with rostral appendages, male A. proboscis hatch with this structure already developed.
Impacts of additional noise on the social interactions of a cooperatively breeding fish
<p>Anthropogenic noise is a global pollutant known to affect the behaviour of individual animals in all taxa studied. However, there has been relatively little experimental testing of the effects of additional noise on social interactions between conspecifics, despite these forming a crucial aspect of daily life for most species. Here we use established paradigms to investigate how white-noise playback affects both group defensive actions against an intruder and associated within-group behaviours in a model fish species, the cooperatively breeding cichlid <i>Neolamprologus pulcher</i>. Additional noise did not alter defensive behaviour, but did result in changes to within-group behaviour. Both dominant and subordinate females, but not the dominant male, exhibited less affiliation and showed a tendency to produce more submissive displays to groupmates when there was additional noise compared to control conditions. Our experimental results therefore indicate the potential for anthropogenic noise to affect social interactions between conspecifics and that there can be intraspecific variation in the impacts of this global pollutant.</p>
Figure 2 in Use of a rostral appendage during social interactions in the Ecuadorian Anolis proboscis
Figure 2. (a) Displays performed by male and female (fifth mating). (b) Beginning of chasing. Female approaches and runs past the male in the opposite direction to that in which he was facing. (c) Male bite and proboscis lifting. (d) Male stops biting and lower the rostral appendage after copulation begins. (e) Biting attempt from MIN5 (left) to MIN10 (right). (f) Proboscis used in physical contact, MIN5 (left), MIN10 (right). (g) Jaw locking between MIN27 (left) and MIN29 (right). (h) Body flattening against the branch and colour changing of MIN21 during approach and displays of MIN20. Photo credits: Diego Quirola.
Figure 1 in Use of a rostral appendage during social interactions in the Ecuadorian Anolis proboscis
Figure 1. (a) Newly hatched Anolis proboscis male. (b) A. proboscis juvenile. (c) A. proboscis adult male. (d) A. proboscis adult female. Photo credits: Santiago Ron (a), Diego Quirola (b–d).
Evidence for maintenance of key components of vocal learning in aging budgerigars despite diminished affiliative social interaction
<p>In some species, the ability to acquire new vocalizations persists into adulthood and may be an important mediator of social interactions. While it is generally assumed that vocal learning persists undiminished throughout the lifespan of these open-ended learners, the stability of this trait remains largely unexplored. We hypothesize that vocal learning exhibits senescence, as is typical of complex cognitive traits, and that this decline may relate to age-dependent changes in sociality. The budgerigar (<em>Melopsittacus undulatus</em>), an open-ended learner which develops new contact call types that are shared with social associates upon joining new flocks, provides a robust assay for measuring the effects of aging on vocal learning ability. We formed captive flocks of 4 previously unfamiliar adult males of the same age class, either "young adults" (6 mo.-1 yr.) or "older adults" (≥ 3 yr.), and concurrently tracked changes in contact call structure and social interactions over time. Older adults exhibited decreased vocal diversity, which may be related to the sparser and weaker affiliative bonds observed in older adults. Older adults, however, displayed equivalent levels of vocal plasticity and vocal convergence compared to young adults, suggesting vocal learning ability is largely maintained into later adulthood in an open-ended learner.</p>
SALSA (Health, Food and Sociability): Community Networks for Healthy Eating, Autonomy, and Social Interaction
ClinicalTrials.gov study NCT06800027. IPD Sharing: NO. Countries: 1. Publications: 7.
Memantine for the Treatment of Social Deficits in Youth With Disorders of Impaired Social Interactions
ClinicalTrials.gov study NCT03553875. IPD Sharing: NO. Countries: 1. Publications: 2.
Social Interaction and Compassion in Depression
ClinicalTrials.gov study NCT03080025. IPD Sharing: YES. Countries: 1. Publications: 2.
Mood, Serotonin and Social Interaction
ClinicalTrials.gov study NCT02051530. IPD Sharing: Not stated. Countries: 1. Publications: 1.
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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.