Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,896
datasets available to search
ShareScore release 0.9.0
Dataset results
1,896 results for “call”
Fig 14 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 14 Photographs and calling song spectrograms of Anaulacomera furcata. A. Male; B. Female; C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales. Photo credit: C. Kernan.
Fig 28 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 28 Photographs and calling song spectrograms of Hyperphrona irregularis. A. Male, inset showing blue stripes on dorsal surface of abdomen (photo credit: H. ter Hofstede); B. Female (photo credit: C. Wilson); C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales.
Fig 31 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 31 Photographs and calling song spectrograms of Microcentrum championi. A. Male (photo credit: H. ter Hofstede); B. Female (photo credit: C. Wilson); C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call (C) and one pulse from the same call (D).
Fig 11 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 11 Photograph and calling song spectrograms of Aegimia elongata. A. Male with identification number written in ink; B. and C. Spectrogram (top panel) and oscillogram (bottom panel) of call type 1 at different time scales; D. and E. Spectrogram (top panel) and oscillogram (bottom panel) of call type 2 at different time scales. Photo credit: H. ter Hofstede.
Fig 40 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 40 Photograph and calling song spectrograms of Viadana brunneri. A. Male; B. and C. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales. Photo credit: C. Wilson.
Fig 1 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 1 Representative call of Orophus conspersus with labelled acoustic parameters: A. Spectrogram; B. Oscillogram; and C. Power spectrum. Temporal parameters – PD: pulse duration, PP: pulse period, WO: wing-opening sound. Spectral parameters – BW: bandwidth, HF: high frequency, LF: low frequency, PF: peak frequency.
Fig 10 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 10 Photographs and calling song spectrograms of Vestria punctata. A. Male; B. Female; inset: close-up of face; C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales. Photo credit: H. ter Hofstede.
Fig 35 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 35 Photographs and calling song spectrograms of Philophyllia ingens. A. Male (photo credit: C. Wilson); B. Female (photo credit: H. ter Hofstede); C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales.
Fig 22 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 22 Photographs and calling song spectrograms of Chloroscirtus discocercus. A. Male; B. Female; C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales. Photo credit: H. ter Hofstede.
Fig 27 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 27 Photograph and calling song spectrograms of Hetaira sp.; A. Female; B. and C. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales. Photo credit: L. Symes.
Fig 44 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 44 Photographs and calling song spectrograms of Cocconotus wheeleri. A. Male, inset showing striped face (one of the five black lines is obscured by white glare; photo credit: H. ter Hofstede); B. Female (photo credit: T. Robillard); C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales.
Fig 39 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 39 Photograph and calling song spectrograms of Steirodon stalii. A. Male; B. and C. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales. Photo credit: C. Wilson.
Fig 30 from: ter Hofstede HM, Symes LB, Martinson SJ, Robillard T, Faure P, Madhusudhana S, Page RA (2020) Calling songs of Neotropical katydids (Orthoptera: Tettigoniidae) from Panama. Journal of Orthoptera Research 29(2): 137-201. https://doi.org/10.3897/jor.29.46371
Fig 30 Photographs and calling song spectrograms of Lamprophyllum micans. A. Male; B. Female; C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call (C) and one pulse from the same call (D). Photo credit: C. Wilson.
FIGURE 189. Calling drum adult male S in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus
FIGURE 189. Calling drum adult male S. zimapan (R11-4) with 52 single drums over 7.4s at 21°C.
FIGURE 190. Calling drum adult female S in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus
FIGURE 190. Calling drum adult female S. zimapan (R06-25). See text for details.
FIGURE 65. Calling drum holotype adult female S in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus
FIGURE 65. Calling drum holotype adult female S. honduras.
FIGURE 64. Adult male calling drum S. honduras, showing 3 in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus
FIGURE 64. Adult male calling drum S. honduras, showing 3-part song.
Data from: Social call divergence in bats: a comparative analysis
Acoustic signals mediate important life history events in a variety of species, providing new vistas for understanding speciation. It has been proposed that animal acoustic signals undergo complex interactions among morphology, ecology, social pressure, and phylogenetic history. Yet, the relative importance of these factors in shaping acoustic divergence is rarely assessed within a comparative framework. Herein, we aim to investigate the key determinants of social call divergence across 31 bat species from 5 families. We compiled a wide data set on bat aggressive calls, body size, foraging habitats, foraging modes, climatic conditions, colony size, and phylogenetic components. We identified remarkable interspecific divergence versus within-species variation in aggressive vocalizations. Despite weak effects of ecological factors, colony size, body size, and phylogenetic components accounted for the majority of variation in call parameters among species. The colony size and body size played a major role in influencing spectral parameters, whereas phylogenetic relationships determined call duration and minimum frequency. Together, our findings constitute convincing evidence that sociality, morphological constraint, and phylogenetic constraint mold social call divergence in bats. This study expands our limited knowledge of the evolution of bat social calls, and highlights the importance of sociality in driving acoustic phenotype diversity.
Data from: Spatio-temporal dynamics of field cricket calling behaviour: implications for female mate search and mate choice
Amount of calling activity (calling effort) is a strong determinant of male mating success in species such as orthopterans and anurans that use acoustic communication in the context of mating behaviour. While many studies in crickets have investigated the determinants of calling effort, patterns of variability in male calling effort in natural choruses remain largely unexplored. Within-individual variability in calling activity across multiple nights of calling can influence female mate search and mate choice strategies. Moreover, calling site fidelity across multiple nights of calling can also affect the female mate sampling strategy. We therefore investigated the spatio-temporal dynamics of acoustic signaling behaviour in a wild population of the field cricket species Plebeiogryllus guttiventris. We first studied the consistency of calling activity by quantifying variation in male calling effort across multiple nights of calling using repeatability analysis. Callers were inconsistent in their calling effort across nights and did not optimize nightly calling effort to increase their total number of nights spent calling. We also estimated calling site fidelity of males across multiple nights by quantifying movement of callers. Callers frequently changed their calling sites across calling nights with substantial displacement but without any significant directionality. Finally, we investigated trade-offs between within-night calling effort and energetically expensive calling song features such as call intensity and chirp rate. Calling effort was not correlated with any of the calling song features, suggesting that energetically expensive song features do not constrain male calling effort. The two key features of signaling behaviour, calling effort and call intensity, which determine the duration and spatial coverage of the sexual signal, are therefore uncorrelated and function independently.
Data from: High and dry: trade-off in arboreal calling in a treefrog mediated by local environment
Trade-offs shaping behavioral variation are often influenced by the environment. We investigated the role that the environment plays in mediating trade-offs using a widespread frog with a conspicuous mating display, Pseudacris crucifer. We first demonstrated, using playback and desiccation experiments, that calling site selection involves a trade-off between sound transmission and desiccation. We then determined the influence of local environmental conditions on the intensity of the trade-off by examining range-wide behavioral and environmental data. We showed that the benefit of improved call transmission is positively influenced by vegetation density and ground cover. Behavioral data are consistent with this relationship: sites with a greater transmission benefit have increased prevalence of arboreally-calling males. We also found that the prevalence of arboreal calling behavior increases with relative humidity and air temperature, suggesting an influence of these environmental variables on the desiccation cost of arboreal calling. This study provides a clear example of the role of the environment in mediating trade-off intensities and shaping critical behavioral traits.
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.