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.
57
datasets available to search
ShareScore release 0.9.0
Dataset results
57 results for “Vocal Repertoire”
FIGURE 3 in Larval morphology and complex vocal repertoire of Rhacophorus helenae (Anura: Rhacophoridae), a rare flying frog from Vietnam
FIGURE 3. External morphology of the tadpole of Rhacophorus helenae (ZMMU NAP-03164, Stage 37, TL 40.1 mm). (A) lateral view; (B) dorsal view; (C) coloration in preservative.
FIGURE 6 in Larval morphology and complex vocal repertoire of Rhacophorus helenae (Anura: Rhacophoridae), a rare flying frog from Vietnam
FIGURE 6. Waveform (A) and spectrogram (B) of different call types of Rhacophorus helenae: 1—simple tonal, 2—tonal with pulses, 3—simple wideband, 4—wideband with pulses, 5—pulsed calls, and 1-4 —example of transitional call. The waveform shows the presence of rhythmic amplitude modulation in some call types. Call sequence and intervals are not natural.
FIGURE 2 in Larval morphology and complex vocal repertoire of Rhacophorus helenae (Anura: Rhacophoridae), a rare flying frog from Vietnam
FIGURE 2. Maximum likelihood dendrogram of Rhacophorus derived from the analysis of 843 bp of 16S rRNA mtDNA gene. Voucher samples and GenBank accession numbers are given in Table 1. Numbers near nodes represent bootstrap support values (1000 replicates) for ML / and posterior probabilities (PP) for Bayesian inferences respectively.
FIGURE 1 in Larval morphology and complex vocal repertoire of Rhacophorus helenae (Anura: Rhacophoridae), a rare flying frog from Vietnam
FIGURE 1. Known distribution of Rhacophorus helenae in southern Vietnam. Yellow dots correspond to localities reported by Rowley et al. (2012a); red dots correspond to localities reported in the present study. Locality information: 1—Nui Ong Nature Reserve, Binh Thuan Province; 2—Tan Phu Forest, Dong Nai Province; 3—Binh Chau–Phuoc Buu Nature Reserve, Ba Ria– Vung Tau Province; 4—Ma Da Forest, Dong Nai Province.
FIGURE 5 in Larval morphology and complex vocal repertoire of Rhacophorus helenae (Anura: Rhacophoridae), a rare flying frog from Vietnam
FIGURE 5. Differences in coloration (A, B) and webbing development (C, D) between juvenile (approximately one month after the completion of metamorphosis) and adult Rhacophorus helenae. Photographs by V. Trounov.
FIGURE 4 in Larval morphology and complex vocal repertoire of Rhacophorus helenae (Anura: Rhacophoridae), a rare flying frog from Vietnam
FIGURE 4. Larval mouthparts morphology of Rhacophorus helenae (ZMMU NAP-03164, Stage 37, TL 40.1 mm) (A) and coexisting large rhacophorids: (B) Rhacophorus annamensis (NAP-02609, Stage 35, TL 38.8 mm); (C) Polypedates megacephalus (NAP-02415, Stage 37, TL 33.8 mm).
Data Associated with Manuscript Titled "Evolution of Primate Vocal Repertoires: Vocalization Systems as Embodied Capital for Mediating Within-group Conflict"
<p><span>This is a dataset used in analyses of the macroevolution of primate vocal repertoire size interpreted in the associated manuscript titled "Evolution of Primate Vocal Repertoires: Vocalization Systems as Embodied Capital for Mediating Within-group Conflict." The first tab of the data file contains the following information for each of 42 primates species: maximum longevity (years), endocranial volume (cubic centimeters), log endocranial volume, body mass (g), log body mass, group size, within-group conflict score, vocal repertoire size, and research effort (number of zoological records). The second tab of the data file contains two tables, one reports maximum longevity (years), endocranial volume (cubic centimeters), log endocranial volume, group size, within-group conflict score, and vocal repertoire size values (mean, median, standard deviation, range) aggregated at the suborder, infraorder, superfamily, and family level, while the other reports those statistics aggregated at the family level. The third tab of the data file contains ancestral node ID, ancestral node age (in millions of years), reconstructed ancestral within-group conflict values (mean, 95% lower confidence interval, 95% upper confidence interval), and reconstructed ancestral vocal repertoire size values (mean, 95% lower confidence interval, 95% upper confidence interval). A .pdf file provides visualizations of ancestral character reconstruction (ACR) models with ancestral node IDs for Z-scored within-group conflict (panel A) and Z-scored vocal repertoire size (panel B). </span></p>
The vocal repertoire of the bearded capuchin (Cebidae: Sapajus libidinosus): implications for understanding the complexity of neotropical primate communication
<p>Vocal communication is an essential aspect of primate social behaviour. The bearded capuchin <i>Sapajus libidinosus</i> is endemic to Brazil and some studies have described specific vocalisation types for this species; however, there is still no complete description of its vocal repertoire. Thus, this study aimed to describe the vocal repertoire of a group of <i>S. libidinosus</i> living in the<i> Parque Nacional de Brasília</i> (PNB), a protected area in the Cerrado area of Central Brazil. We carried out focal samplings and recording of vocalisations of members of a <i>S. libidinosus</i> troop in different behavioural contexts. The call analyses revealed 25 different types of vocalisations, and each call presented significant structural variation. We grouped these vocalisations according to the context of the emission or acoustic structure into the following categories: contact calls (contact note, infant babbling, trill, teeth- and lip-smacking, and sirena); foraging calls (chihui, grgr, and patinado); whistle series (WS; food-associated WS, long-distance WS, and inter-group encounter WS); aggressive calls (aggressive contact note, ascending rapid staccato, cough cough, and pip); calls in response to aggression (scream, squeal, and pulsed scream), sexual display calls (chuck and raspy oestrous call), and stress-related calls (alarm call/ bark, hiccup, hip, double hip, and wah wah). <i>S. libidinosus</i> presented a very rich vocal repertoire, revealing a pattern consistent with the repertoire of other capuchin monkey species. This is the first comprehensive description of the<i> S. libidinosus</i> vocal repertoire and highlights the complexity of neotropical primate communication.</p> <p>Vocal communication is an essential aspect of primate social behaviour. The bearded capuchin <i>Sapajus libidinosus</i> is endemic to Brazil and some studies have described specific vocalisation types for this species; however, there is still no complete description of its vocal repertoire. Thus, this study aimed to describe the vocal repertoire of a group of <i>S. libidinosus</i> living in the<i> Parque Nacional de Brasília</i> (PNB), a protected area in the Cerrado area of Central Brazil. We carried out focal samplings and recording of vocalisations of members of a <i>S. libidinosus</i> troop in different behavioural contexts. The call analyses revealed 25 different types of vocalisations, and each call presented significant structural variation. We grouped these vocalisations according to the context of the emission or acoustic structure into the following categories: contact calls (contact note, infant babbling, trill, teeth- and lip-smacking, and sirena); foraging calls (chihui, grgr, and patinado); whistle series (WS; food-associated WS, long-distance WS, and inter-group encounter WS); aggressive calls (aggressive contact note, ascending rapid staccato, cough cough, and pip); calls in response to aggression (scream, squeal, and pulsed scream), sexual display calls (chuck and raspy oestrous call), and stress-related calls (alarm call/ bark, hiccup, hip, double hip, and wah wah). <i>S. libidinosus</i> presented a very rich vocal repertoire, revealing a pattern consistent with the repertoire of other capuchin monkey species. This is the first comprehensive description of the<i> S. libidinosus</i> vocal repertoire and highlights the complexity of neotropical primate communication.</p>
Figure 4 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 4. Oscillogram and sound spectrogram of the encounter call of Oreobates barituensis from Arroyo La Loza, Jujuy province, Argentina. Recorded on 29 November 2008; air temperature during recording was 18.0◦C.
Figure 2 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 2. Oscillogram and sound spectrogram of the encounter call of Oreobates discoidalis from Jaire, Jujuy province, Argentina. Recorded on 14 November 2009; air temperature during recording was 17.4◦C.
Figure 1 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 1. Oscillogram and sound spectrogram of the advertisement call and territorial call of Oreobates discoidalis from Jaire, Jujuy province, Argentina. Recorded on 8 November 2009; air temperature during recording was 13.6◦C.
Figure 3 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 3. Oscillogram and sound spectrogram of the advertisement call and territorial call of Oreobates barituensis from Río Yerba Buena, Jujuy province, Argentina. Recorded on 1 December 2009; air temperature during recording was 21.1◦C.
FIGURE 7 in A new species of Gracixalus (Anura: Rhacophoridae) with a hyperextended vocal repertoire from Vietnam
FIGURE 7. Maximum-likelihood (ML) tree based on 16S ribosomal RNA mitochondrial gene sequences for species currently assigned to Gracixalus (Frost 2011) and for outgroups (Philautus aurifasciatus (type species of Philautus), Kurixalus eiffingeri (type species of Kurixalus) and K. odontotarsus). Bayesian inference (BI) produced near-identical topology. Numbers on branches are ML bootstrap values and Bayesian posterior probabilities. Species names in bold represent sequences from specimens collected at or in close proximity to type locality. Species names for previously published sequences remain as in original publications. Frog images represent approximate relative male body sizes for each species/group, and approximate primary dorsal colour (dull greenish/bright green/brownish or greyish).
FIGURE 3 in A new species of Gracixalus (Anura: Rhacophoridae) with a hyperextended vocal repertoire from Vietnam
FIGURE 3. Dorsum (A), venter (B), and lateral view of head (C) of preserved male Gracixalus gracilipes (AMNH A193894), Gracixalus supercornutus (AMS R 173395), and Gracixalus quangi sp. nov. (holotype AMS R 173410).
FIGURE 2 in A new species of Gracixalus (Anura: Rhacophoridae) with a hyperextended vocal repertoire from Vietnam
FIGURE 2. Dorsal (A), ventral (B), lateral (C) and dorsolateral (D) views of male holotype of Gracixalus quangi sp. nov. (AMS R 173410) in life.
FIGURE 5 in A new species of Gracixalus (Anura: Rhacophoridae) with a hyperextended vocal repertoire from Vietnam
FIGURE 5. (A) General habitat of Gracixalus quangi sp. nov. in Pu Hoat Proposed Nature Reserve, (B) breeding site of Gracixalus quangi sp. nov., with shallow puddle/seep on rocky forest floor, (C) close-up of same breeding site, with yellow arrows pointing towards egg masses deposited on the tips of leaves, (D) Gracixalus quangi sp. nov. clutch of eleven tadpoles from same breeding site (AMS R 173425), with egg mass visible on leaf in background.
FIGURE 4 in A new species of Gracixalus (Anura: Rhacophoridae) with a hyperextended vocal repertoire from Vietnam
FIGURE 4. Male advertisement call of Gracixalus quangi sp. nov. (A) waveform of relative amplitude (Rel. amp) over time of a call sequence for (i) holotype AMS R 173410 (ii) paratype AMS R 173413, and (iii) paratype AMS R 173414. (B) representative calls shown as waveforms above and corresponding spectrograms (frequency over time) below for (i–vi) holotype AMS R 173410, (vii–ix) paratype AMS R 173413 and (x–xvi) paratype AMS R 173414. All calls were recorded at an ambient air temperature of 24.1º C.
FIGURE 1 in A new species of Gracixalus (Anura: Rhacophoridae) with a hyperextended vocal repertoire from Vietnam
FIGURE 1. Type locality of Gracixalus quangi sp. nov. (yellow star), Gracixalus gracilipes (closed circle), Gracixalus supercornutus (closed square) and Gracixalus quyeti (open circle).
FIGURE 1 in Vocal repertoire of the horned frog Proceratophrys laticeps (Amphibia: Anura: Odontophrynidae)
FIGURE 1. Release calls of Proceratophrys laticeps, A) from EBSL and B) EBMAR. C) Distress call and D) Advertisement call series of P. laticeps from EBMAR.
Figure 2 in Vocal repertoire and group-specific signature in the Smooth-billed Ani, Crotophaga ani Linnaeus, 1758 (Cuculiformes, Aves)
Figure 2. Song structure of the Smooth-billed Ani showing the notes, sillable and harmonic.
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.