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201 results for “singing”
Singing behaviour of Ruby-crowned Kinglets (Regulus calendula) in relation to time-of-day, time-of-year, and social context
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Can behaviour impede evolution? persistence of singing effort after morphological song loss in crickets
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Singing silver-haired bats (Lasionycteris noctivagans)
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Data from: Singing behaviour of Ruby-crowned Kinglets (Regulus calendula) in relation to time-of-day, time-of-year, and social context
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Data from: Natural singing interactions in Parus major
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Data from: Sexual signal loss in field crickets maintained despite strong sexual selection favoring singing males
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Singing on the nest is a widespread behavior in incubating Northern Mockingbirds and increases probability of nest predation
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Singing behind the stage: thrush nightingales produce more variable songs on their wintering grounds
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Data to: Aerosol emission of child voices during speaking, singing and shouting
<p>This dataset contains raw data of emitted aerosols measured via a laser particle counter. Further, R-code (RMarkdown) for statistical analyses is available. A pre-print of an article based on these data was deposited here:</p> <p>https://www.medrxiv.org/content/early/2020/09/18/2020.09.17.20196733</p> <p> </p> <p> </p>
Singing under glass: rapid effects of anthropogenic habitat modification on song and response behaviours in an isolated house sparrow (Passer domesticus) population
<p>Anthropogenic noise pollution and the introduction of novel infrastructure can impose strong selective pressures on avian communication by affecting the efficacy with which acoustic signals are transmitted and received. Many species have now been shown to sing at higher frequencies in noisy urban environments. However, few studies have investigated the effects of signal modification on the response behaviours of receivers, and fewer still have been able to indicate the timescale over which these changes in pitch have occurred. We compare vocal communication between house sparrows (Passer domesticus) that reside within the world's largest, single-span glasshouse (completed in the year 2000), and house sparrows directly outside this glasshouse, in open farmland. The glasshouse contrasts both acoustically and physically with the external environment, low frequency background noise being significantly louder inside than outside. We show that minimum song frequency was significantly higher inside the glasshouse than in surrounding farm habitat. Using song playback, we also found that birds within the glasshouse reacted more strongly to playbacks from the glasshouse habitat than they did to playback of song from farm birds outside. The degree of difference in frequency is similar to that shown for other bird species between urban and rural environments, demonstrating that such behavioural differences may arise over a relatively short time period (14 years in this case)</p>
Data from: Interspecific dominance via vocal interactions mediates altitudinal zonation in Neotropical singing mice
Interspecific aggression between ecologically similar species may influence geographic limits by mediating competitive exclusion at the range edge. Advertisement signals that mediate competitive interactions within species may also provide social information that contributes to behavioral dominance and spatial segregation among species. We studied the mechanisms underlying altitudinal range limits in Neotropical singing mice (Scotinomys), a genus of muroid rodent in which males vocalize to repel rivals and attract mates. We first delineated replacement zones and described temperature regimes on three mountains in Costa Rica and Panama where Chiriquí singing mice (S. xerampelinus) abruptly replace Alston's singing mice (S. teguina). Next, we conducted interspecific behavioral trials and reciprocal removal experiments to examine if interspecific aggression mediated species replacement. Finally, we performed reciprocal playback experiments to investigate whether response to song matched competitive interactions. Behavioral trials and removal experiments suggest that S. xerampelinus is behaviorally dominant and excludes S. teguina from higher, cooler altitudes. Playback experiments indicate that subordinate S. teguina is silenced and repelled by heterospecific song, whereas S. xerampelinus responded to heterospecifics with approach and song rates comparable to responses to conspecifics. Thus, interspecific communication reflects underlying dominance and suggests that acoustic signaling contributes to altitudinal zonation of ecologically similar congeners. Our findings implicate the use of social information in structuring spatial distributions of animal communities across landscapes and provide insight into how large-scale patterns are generated by individual interactions.
Singing Bowls App Demo
<p>This video shows a demo of Singing Bowls, a touch-screen musical instrument app for iPad. Singing Bowls consists of an annular interface where each ring represents a different pitch. Tapping the rings produces a short sound, while swirling or swiping produces continuous sounds. As a prototype app, Singing Bowls was used in research and performance activities in 2014 with Ensemble Metatone. A refined version of Singing Bowls, PhaseRings, was later publicly released on the iTunes App Store.</p>
ChoralSynth: Synthetic Dataset of Choral Singing
<p><strong>Overview</strong></p><p>ChoralSynth is a synthesized dataset of 20 multitrack choral songs curated by carefully listening and analyzing a set of synthetic choral songs generated using one of the state-of-the-art synthesizers. The resulting dataset can serve as a valuable resource for various MIR research endeavors like source separation, melodic analysis, chord analysis, rhythmic analysis amongst others.</p>
Singing stones and Guanche rock art, Tenerife
Roque del Malpaso near Buzanada, Arona, Tenerife. This model shows a Guanche rock art panel (c.2m across) that is surrounded by singing stones. The volcanic rock has phonic properties and rings loudly when struck with a hammerstone. There are dozens of points on different rocks that have been struck and each location gives a different sound. These stones are located at the top of a dramatic craggy outcrop some 20m high; only a small area has been 3d modelled. Source: Objaverse 1.0 / Sketchfab
00885 LII. Woche II. 7. Br. Josephs Rede in der Abend-Versammlung zu Hennersdorf, am ersten Weyhnachtsfeyertage ... d. 25. Dec. über die Loosung: Mache dich auf, mache dich auf, Zion! Zeuch deiner Stärcke an, schmücke dich herrlich, du heilige Stadt Jerusalem! Sing heut und freu dich, Christenheit! ob Gott mit großer Innigkeit, denn dein Heiland ist die gesandt, der Jesus Christus wird
<p>Mit den <em><strong>Gemein-Nachrichten</strong></em> stellt das Unitätsarchiv Herrnhut der weltweiten Evangelischen Brüder-Unität - Herrnhuter Brüdergemeine (Unitas Fratrum / Moravian Church) das älteste und umfangreichste Mitteilungsblatt der Brüdergemeine digital zur Verfügung. Es enthält Berichte aus Gemeinden sowie dem Missions- und Diasporawerk der Brüdergemeine sowie Reden und Lebensläufe. Die <em>Gemein-Nachrichten</em> wurden ab 1765 in Fortsetzung des <em>Jüngerhaus-Diariums</em> (1747-1764) ausschließlich handschriftlich vervielfältigt. In Druck gingen 1817 und 1818 die <em>Beyträge aus der Brüder-Gemeine</em> und zwischen 1819 und 1894 die <em>Nachrichten aus der Brüder-Gemeine</em>. Das Nachrichtenblatt fand in den <em>Mitteilungen aus der Brüder-Gemeine zur Förderung christlicher Gemeinschaft</em> ab 1895 bis 1941 seine Fortsetzung.</p> <p>Das hier <strong>vorliegende Datenset</strong> umfasst Transkriptionen nach XML-TEI in verschiedenen Versionierungen und einen normalisierten Text. Die ID bezieht sich auf den <strong>Index</strong> der handschriftlichen Gemein-Nachrichten (<a href="../doi/10.5281/zenodo.8228849">DOI</a>). Metadaten werden nach einem standardisierten <strong>XML-Schema</strong> angelegt (<a href="../doi/10.5281/zenodo.10375427">DOI</a>). Die Dateinamen sind sprechend:<br><br>[ID]_01.xml: Export (XML-TEI) nach Transkription vom Primärdigitalisat</p> <p>[ID]_02.xml: um Metadaten angereichtertes Transkript (XML-TEI) </p> <p>[ID]_03.txt: normalisierter Text zur weiteren Nutzung (z.B. für maschinelle Analysen)</p> <p>[ID]_04.xml: angereichertes Transkript (XML-TEI) mit Metadaten und Glossarannotation</p>
On following pages: 115. Reed Vole (Alexandromys fortis); 116. Sakhalin Vole (Alexandromys sachalinensis); 117. Mongolian Vole (Alexandromys mongolicus); 118. Middendorff's Vole (Alexandromys middendorffii; 119. Gromov's Vole (Alexandromys gromovi); 120. Lacustrine Vole (Alexandromys limnophilus); 121. Root Vole (Alexandromys oeconomus); 122. Taiwan Vole (Alexandromys kikuchii); 123. Japanese Grass Vole (Alexandromys montebell); 124. Afghan Vole (Microtus afghanus); 125. Bucharian Vole (Microtus bucharensis); 126. Juniper Vole (Microtus juldaschi); 127. Short-tailed Field Vole (Microtus agrestis); 128. Mediterranean Field Vole (Microtus lavernedii): 129. Portuguese Field Vole (Microtus rozianus); 130. Insular Vole (Microtus abbreviatus); 131. Singing Vole (Microtus miurus); 132. Rock Vole (Microtus chrotorrhinus); 133. Zempoaltepec Vole (Microtus umbrosus); 134. Tarabundi Vole (Microtus oaxacensis); 135. Guatemalan Vole (Microtus guatemalensis); 136. Woodland Vole (Microtus pinetorum); 137. Jalapan Vole (Microtus quasiater); 138. California Vole (Microtus californicus): 139. Beach Vole (Microtus brewer); 140. Mexican Vole (Microtus mexicanus); 141. Mogollon Vole (Microtus mogollonensis); 142. Prairie Vole (Microtus ochrogasten; 143. Taiga Vole (Microtus xanthognathus); 144. Cabrera''s Vole (Microtus cabrerae); 145. North American Water Vole (Microtus richardson); 146. Gray-tailed Vole (Microtus canicaudus). in Cricetidae
On following pages: 115. Reed Vole (Alexandromys fortis); 116. Sakhalin Vole (Alexandromys sachalinensis); 117. Mongolian Vole (Alexandromys mongolicus); 118. Middendorff's Vole (Alexandromys middendorffii; 119. Gromov's Vole (Alexandromys gromovi); 120. Lacustrine Vole (Alexandromys limnophilus); 121. Root Vole (Alexandromys oeconomus); 122. Taiwan Vole (Alexandromys kikuchii); 123. Japanese Grass Vole (Alexandromys montebell); 124. Afghan Vole (Microtus afghanus); 125. Bucharian Vole (Microtus bucharensis); 126. Juniper Vole (Microtus juldaschi); 127. Short-tailed Field Vole (Microtus agrestis); 128. Mediterranean Field Vole (Microtus lavernedii): 129. Portuguese Field Vole (Microtus rozianus); 130. Insular Vole (Microtus abbreviatus); 131. Singing Vole (Microtus miurus); 132. Rock Vole (Microtus chrotorrhinus); 133. Zempoaltepec Vole (Microtus umbrosus); 134. Tarabundi Vole (Microtus oaxacensis); 135. Guatemalan Vole (Microtus guatemalensis); 136. Woodland Vole (Microtus pinetorum); 137. Jalapan Vole (Microtus quasiater); 138. California Vole (Microtus californicus): 139. Beach Vole (Microtus brewer); 140. Mexican Vole (Microtus mexicanus); 141. Mogollon Vole (Microtus mogollonensis); 142. Prairie Vole (Microtus ochrogasten; 143. Taiga Vole (Microtus xanthognathus); 144. Cabrera''s Vole (Microtus cabrerae); 145. North American Water Vole (Microtus richardson); 146. Gray-tailed Vole (Microtus canicaudus).
On following pages: 211. Short-tailed Singing Mouse (Scotinomys teguina); 212. Long-tailed Singing Mouse (Scotinomys xerampelinus); 213. Yellow Deermouse (Isthmomys flavidus); 214. Mount Pirri Deermouse (/sthmomys pirrensis); 215. Florida Deermouse (Podomys floridanus); 216. Volcano Deermouse (Neotomodon alstoni); 217. Short-nosed Harvest Mouse (Reithrodontomys brevirostris); 218. Darien Harvest Mouse (Reithrodontomys darienensis); 219. Slender Harvest Mouse (Reithrodontomys gracilis); 220. Mexican Harvest Mouse (Reithrodontomys mexicanus); 221. Nicaraguan Harvest Mouse (Reithrodontomys paradoxus); 222. Cozumel Harvest Mouse (Reithrodontomys spectabilis); 223. Talamancan Harvest Mouse (Reithrodontomys crepen; 224. Rodriguez's Harvest Mouse (Reithrodontomys rodriguez); 225. Narrow-nosed Harvest Mouse (Reithrodontomys tenuirostris); 226. Small-toothed Harvest Mouse (Reithrodontomys microdon); 227. Costa Rican Harvest Mouse (Reithrodontomys cherrii); 228. Chiriquian Harvest Mouse (Reithrodontomys garichensis); 229. Musser's Harvest Mouse (Reithrodontomys musseri); 230. Baker's Harvest Mouse (Reithrodontomys bakeri); 231. Fulvous Harvest Mouse (Reithrodontomys fulvescens); 232. Hairy Harvest Mouse (Reithrodontomys hirsutus); 233. Sonoran Harvest Mouse (Reithrodontomys burti); 234. Volcano Harvest Mouse (Reithrodontomys chrysopsis); 235. Eastern Harvest Mouse (Reithrodontomys humulis); 236. Western Harvest Mouse (Reithrodontomys megalotis); 237. Plains Harvest Mouse (Reithrodontomys montanus); 238. Salt-marsh Harvest Mouse (Reithrodontomys raviventris); 239. Sumichrast's Harvest Mouse (Reithrodontomys sumichrasti); 240. Zacatecan Harvest Mouse (Reithrodontomys zacatecae); 241. Chihuahuan Grasshopper Mouse (Onychomys arenicola); 242. Northern Grasshopper Mouse (Onychomys leucogaster); 243. Southern Grasshopper Mouse (Onychomys torridus); 244. Osgood's Deermouse (Osgoodomys banderanus). in Cricetidae
On following pages: 211. Short-tailed Singing Mouse (Scotinomys teguina); 212. Long-tailed Singing Mouse (Scotinomys xerampelinus); 213. Yellow Deermouse (Isthmomys flavidus); 214. Mount Pirri Deermouse (/sthmomys pirrensis); 215. Florida Deermouse (Podomys floridanus); 216. Volcano Deermouse (Neotomodon alstoni); 217. Short-nosed Harvest Mouse (Reithrodontomys brevirostris); 218. Darien Harvest Mouse (Reithrodontomys darienensis); 219. Slender Harvest Mouse (Reithrodontomys gracilis); 220. Mexican Harvest Mouse (Reithrodontomys mexicanus); 221. Nicaraguan Harvest Mouse (Reithrodontomys paradoxus); 222. Cozumel Harvest Mouse (Reithrodontomys spectabilis); 223. Talamancan Harvest Mouse (Reithrodontomys crepen; 224. Rodriguez's Harvest Mouse (Reithrodontomys rodriguez); 225. Narrow-nosed Harvest Mouse (Reithrodontomys tenuirostris); 226. Small-toothed Harvest Mouse (Reithrodontomys microdon); 227. Costa Rican Harvest Mouse (Reithrodontomys cherrii); 228. Chiriquian Harvest Mouse (Reithrodontomys garichensis); 229. Musser's Harvest Mouse (Reithrodontomys musseri); 230. Baker's Harvest Mouse (Reithrodontomys bakeri); 231. Fulvous Harvest Mouse (Reithrodontomys fulvescens); 232. Hairy Harvest Mouse (Reithrodontomys hirsutus); 233. Sonoran Harvest Mouse (Reithrodontomys burti); 234. Volcano Harvest Mouse (Reithrodontomys chrysopsis); 235. Eastern Harvest Mouse (Reithrodontomys humulis); 236. Western Harvest Mouse (Reithrodontomys megalotis); 237. Plains Harvest Mouse (Reithrodontomys montanus); 238. Salt-marsh Harvest Mouse (Reithrodontomys raviventris); 239. Sumichrast's Harvest Mouse (Reithrodontomys sumichrasti); 240. Zacatecan Harvest Mouse (Reithrodontomys zacatecae); 241. Chihuahuan Grasshopper Mouse (Onychomys arenicola); 242. Northern Grasshopper Mouse (Onychomys leucogaster); 243. Southern Grasshopper Mouse (Onychomys torridus); 244. Osgood's Deermouse (Osgoodomys banderanus).
SVDD Challenge 2024: A Singing Voice Deepfake Detection Challenge (CtrSVDD Track, Test Set)
<p>For more information about SVDD Challenge 2024, please refer to https://challenge.singfake.org/.<br><br>We have released the test set here.</p> <p>The training and development set is at https://zenodo.org/records/10467648.</p> <p>The Interspeech paper that describes the dataset details and baseline analysis is https://arxiv.org/abs/2406.02438.</p>
Idina Menzel - Let It Go (from "Frozen") (Sing-Along Version)
<p>Music video by Idina Menzel performing Let It Go (from "Frozen"). (C) 2014 Walt Disney Records</p>
Singing Insects of North America: SINA maps curated
removed taxa w/o scientific name
ScienceDex guides
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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.