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17 results for “Group communication”

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zenodo40/100

Figure 1-2 in Acoustic communication in two species of the Hypsiboas albopunctatus group (Anura: Hylidae) in sympatry and allopatry

Figure 1-2. Advertisement (1) and aggressive (2) calls of Hypsiboas abopunctatus from Barro Alto, Goiás, Brazil. Above audiospectrogram, below oscillogram. (1) Air temperature = 23.4°C, Air humidity = 68%, SVL = 51,84 mm; (2) Air temperature = 19,8°C; Air humidity = 88%; SVL = 50,27 mm.

opencc-by-4.0Apr 2016View details →
zenodo40/100

Figure 3-5 in Acoustic communication in two species of the Hypsiboas albopunctatus group (Anura: Hylidae) in sympatry and allopatry

Figure 3-5. Advertisement (3), aggressive I (4) and aggressive II (5) calls of Hypsiboas paranaiba from Barro Alto, Goiás, Brazil. Above audiospectrogram; below oscillogram. (3) Air temperature = 21°C, Air humidity = 92%, SVL = 45.03 mm; (4) Air temperature = 21°C, Air humidity = 92%, SVL = 45.04 mm; (5) Air temperature = 21°C, Air humidity = 92%, SVL = 43.22 mm.

opencc-by-4.0Apr 2016View details →
dryad40/100

Vocal communication is seasonal in social groups of wild, free-living house mice

Open the record for dataset details and reuse information.

publicMay 2025View details →
zenodo36/100

Replication data for Nematzadeh et al. "Information Overload in Group Communication: From Conversation to Cacophony in the Twitch Chat"

<p>A subset of the chat logs dump from Twitch used in this work is provided, to help replicate the central findings of this work (<a href="https://doi.org/10.5281/zenodo.1182793">https://doi.org/10.5281/zenodo.1182793</a>). Data are aggregated and include the number of messages posted in each channel and the number of users posting them, sampled at intervals of 5 minutes. To protect the identity of the users in this data collection, message contents and user names are not included in this dataset. Stream names have been replaced with numeric IDs.&nbsp;<br> No additional filtering or data cleaning operation has been applied to this data. Replication code is available on Github (<a href="https://github.com/glciampaglia/twitch-overload-replication">https://github.com/glciampaglia/twitch-overload-replication</a>).</p>

opencc-by-2.0Mar 2019View details →
dryad32/100

Data from: Patterns of call communication between group-housed Zebra finches change during the breeding cycle

Vocal signals such as calls play a crucial role for survival and successful reproduction, especially in group-living animals. However, call interactions and call dynamics within groups remain largely unexplored because their relation to relevant contexts or life-history stages could not be studied with individual-level resolution. Using on-bird microphone transmitters, we recorded the vocalisations of individual zebra finches (Taeniopygia guttata) behaving freely in social groups, while females and males previously unknown to each other passed through different stages of the breeding cycle. As birds formed pairs and shifted their reproductive status, their call repertoire composition changed. The recordings revealed that calls occurred non-randomly in fine-tuned vocal interactions and decreased within groups while pair-specific patterns emerged. Call-type combinations of vocal interactions changed within pairs and were associated with successful egg-laying, highlighting a potential fitness relevance of calling dynamics in communication systems.

opencc-zeroDec 2014View details →
zenodo32/100

Source Data for Xiao et al., Topological Superfluid Defects with Discrete Point Group Symmetries , Nature Communications 13, 4635 (2022).

<p>Source data for Figures 2-5. Source data for Supplementary Figures S2-S5 available upon request to David Hall (dshall@amherst.edu).</p>

opencc-by-4.0Jul 2022View details →
zenodo32/100

Figure 3 in Vocal communication in the striped field mouse, Apodemus agrarius, in dyadic encounters and intraspecific cage groups

Figure 3. Examples of the calls resembling clucks: (A) shorter and more rapidly modulated and (B) longer and slightly modulated.

opennotspecifiedFeb 2008View details →
zenodo32/100

Figure 2 in Vocal communication in the striped field mouse, Apodemus agrarius, in dyadic encounters and intraspecific cage groups

Figure 2. Harsh calls produced by Apodemus agrarius at (A) threatening postures and (B) harsh calls (the second, third and fifth signals) alternated by calls, resembling clucks (the first and fourth signals).

opennotspecifiedFeb 2008View details →
zenodo32/100

Figure 1 in Vocal communication in the striped field mouse, Apodemus agrarius, in dyadic encounters and intraspecific cage groups

Figure 1. Examples of the vocal sounds produced by Apodemus agrarius in response to (A) opponent approach and (B) during attacks and fights.

opennotspecifiedFeb 2008View details →
ClinicalTrials.gov32/100

Group Based Treatment for Persons With Social Communication Difficulties

ClinicalTrials.gov study NCT03636399. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Hearing Loss and Communication Needs in a Group Care Setting for Older Adults

ClinicalTrials.gov study NCT04659967. IPD Sharing: NO. Countries: 1. Publications: 13.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Ethics Communication in Groups Among Healthcare Professionals (The Ethics-com Study).

ClinicalTrials.gov study NCT05146102. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Patterns of call communication between group-housed Zebra finches change during the breeding cycle

Open the record for dataset details and reuse information.

publicJan 2020View details →
dryad28/100

Data from: Is sociality required for the evolution of communicative complexity? Evidence weighed against alternative hypotheses in diverse taxonomic groups

Complex social communication is expected to evolve whenever animals engage in many and varied social interactions; that is, sociality should promote communicative complexity. Yet informal comparisons among phylogenetically independent taxonomic groups seem to cast doubt on the putative role of social factors in the evolution of complex communication. Here, we provide a formal test of the sociality hypothesis along side alternative explanations for the evolution of communicative complexity. We compiled data documenting variation in signal complexity among closely related species for several case study groups – ants, frogs, lizards and birds – and used new phylogenetic methods to investigate the factors underlying communication evolution. Social factors were only implicated in the evolution of complex visual signals in lizards. Ecology, and to some degree allometry, were most likely explanations for complexity in the vocal signals of frogs (ecology) and birds (ecology and allometry). There was some evidence for adaptive evolution in the pheromone complexity of ants, although no compelling selection pressure was identified. For most taxa, phylogenetic null models were consistently ranked above adaptive models and, for some taxa, signal complexity seems to have accumulated in species via incremental or random changes over long periods of evolutionary time. Becoming social presumably lead to the origin of social communication in animals, but its subsequent influence on the trajectory of signal evolution has been neither clear-cut nor general among taxonomic groups.

opencc-zeroDec 2011View details →
dryad28/100

Data from: Is sociality required for the evolution of communicative complexity? Evidence weighed against alternative hypotheses in diverse taxonomic groups

Open the record for dataset details and reuse information.

publicJun 2012View details →
ClinicalTrials.gov24/100

Effectiveness of Online Group-based Nonviolent Communication Interventions

ClinicalTrials.gov study NCT05371002. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

Development of a Group Prenatal Care Intervention to Address Maternal and Child Non-Communicable Disease (NCD) Risk in American Samoa

ClinicalTrials.gov study NCT04025268. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record