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96 results for “song recordings”
Ovenbird song recordings from Alberta (Canada) with individual labels and spatial locations, 2015-2016
This dataset includes spatially localized and individually identified Ovenbird songs. We used automated species detection and acoustic localization to localize Ovenbird singing events from microphone arrays in Alberta, Canada (2015-2016). We then hand-annotated songs to individuals based on acoustic characteristics. This dataset includes the manual annotations and annotations from automated individual identification approaches. This data publication pertains to the manuscript [in prep] by Lapp et al on Ovenbird individual identification and provides further details on the study and the individual identification approach.
Figure 13 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 13. Wave plots illustrating the male calling song of Clinopsalta semilunata sp. nov. Each plot shows a separate recording, with a brief introductory echeme and syllable sequence, followed by a series of repeated echemes. Recordings are from (A) Pratten (28°05'S 151°44'E), (B) Yelarbon State Forest (28°32'S 151°06'E), (C) Binjour Plateau (25°32'S 151°30'E), and (D) Chinchilla (26°39'S 150°35'E), all in Queensland. All recordings were obtained in the field by LWP using RS2 (A), RS3 (B) or RS1 (C); or by A. Ewart using RS5 (D) (see Methods and terminology).
Figure 12 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 12. Wave plots illustrating the structure of the simple part of the male calling song of Clinopsalta autumna sp. nov. from (A) Berry, New South Wales (34°46'S 150°44'E), (B) Spicers Gap, Queensland (28°05'S 152°25'E), (C) Rosewood, Queensland (27°37'S 152°37'E), and (D) Bauple, Queensland (25°48'S 152°35'E). All recordings were obtained in the field by LWP RS1 (A), RS5 (B) or RS2 (C and D) (see Methods and terminology).
Figure 11 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 11. Wave plots illustrating the structure of the complex, introductory part of the male calling song of Clinopsalta autumna sp. nov. from (A) Bargo, New South Wales (34°17'S 150°35'E), (B) Spicer's Gap, Queensland (28°05'S 152°25'E), (C and D) Rosewood, Queensland (27°37'S 152°37'E), and (E) Berry, New South Wales (34°46'S 150°44'E). D provides an example of where timbal-derived syllables (as shown in C) have been replaced with timed wing-snaps. All recordings were obtained in the field by LWP using RS1 (A and E), RS4 (B), or RS2 (C and D) (see Methods and terminology).
Figure 9 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 9. Male calling song structure of Clinopsalta adelaida, illustrated in wave plot form. (A) a single, complete bout of calling. (B) expanded diagram of the commencing section (from A above), showing several repeated sets of song notes, each comprising a macrosyllable separated by three syllables, with a magnified example of two sets shown in the excerpt to the right. (C) expanded diagram of the middle of the song (from A), showing several macrosyllables, each separated by a sequence of syllables, gradually reducing to one syllable; an expanded version showing two macrosyllables, each followed by a syllable sequence is shown to the right of the figure. Wing snaps are detectible in the latter half of this section; however these proved too subtle for illustration. (D) expanded diagram of the latter half of the song (from A), showing repeated macrosyllables, these again expanded for convenience of examination to the right of the main figure. The recording was obtained in the field from Wyalong, New South Wales (33°55'S 147°14'E) by LWP using RS4 (see Methods and terminology).
Figure 8 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 8. Male calling song structure of Clinopsalta adelaida, illustrated in wave plot form. (A) a single, complete bout of calling. (B) expanded diagram of the commencing section (from A above), showing several repeated sets of song notes, each comprising a macrosyllable separated by three syllables, with a magnified example of two sets shown in the excerpt to the right. (C) expanded diagram of the middle of the song (from A), showing several macrosyllables, each separated by a sequence of syllables, gradually reducing to one syllable; an expanded version showing two macrosyllables, each followed by a syllable sequence is shown to the right of the figure. Wing snaps are detectible in the latter half of this section; however these proved too subtle for illustration. D: expanded diagram of the latter half of the song (from A), showing repeated macrosyllables, these again expanded for convenience of examination to the right of the main figure. The recording was obtained in the field from Telowie Gorge, South Australia (33°01'S 138°06'E) by LWP using RS2 (see Methods and terminology).
Figure 7 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 7. Clinopsalta adelaida (A) male, Warrumbungle NPk, NSW (31°18.14'S 149°02.05'E) dorsal habitus; (B) male, ventral habitus; (C) female, Warrumbungle NPk, NSW (31°18.14'S 149°02.05'E), dorsal habitus.
Figure 10 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 10. Male calling song structure of Clinopsalta autumna sp. nov., illustrated in wave plot form. (A) a single, complete bout of calling. (B) expanded diagram of the introductory section (from A above), showing several repeated sets of song notes, each comprising a macrosyllable separated by three syllables. (C) expanded diagram of the middle of the song (from A), showing several macrosyllables, each separated by 1–2 syllables. (D) expanded diagram of the latter half of the song (from A), showing repeated macrosyllables. The recording was obtained in the field from Berry, NSW (34°46'S 150°44'E) by LWP using RS1 (see Methods and terminology).
Figure 6 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 6. Clinopsalta semilunata sp. nov.: illustration of male pygofer and internal genitalia; (a) viewed laterally from the left; (b) viewed ventrally; (c) aedeagus, viewed laterally from left; and (d) apex of theca, viewed dorsally. Characters include: bpl, basal lobe of pygofer; cl, clasper; db, dorsal beak; ps, pseudoparameres; th, theca; un, uncus; upl, upper lobe of pygofer; vs, ventral support. Specimen from 6 km W of Thane (28°09'41"S 151°57'59"E).
Figure 15 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 15. Frequency spectra comparisons between Clinopsalta cicadas, including (A) C. adelaida (from Wyalong, NSW 33°55'S 147°14'E), (B) C. autumna sp. nov. (from Bargo, New South Wales: 34°17'S 150°35'E), (C) C. autumna sp. nov. (from Redwood Park, Queensland: 27°34'S 152°00'E) and (D) C. semilunata sp. nov. (from Pratten, Queensland: 28°05'S 151°44'E). The horizontal bars show the ranges of each highest amplitude frequency plateau (bounded by the 90th percentile of each amplitude spectrum). Recordings were obtained using RS4 (A), RS1 (B and C) or RS2 (D) (see Methods and terminology).
Figure 14 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 14. Wave plots illustrating the repeated phrase structure of the male dusk calling song of Clinopsalta cicadas, including (A) C. autumna sp. nov. from Cunningham's Gap, Queensland (28°03'S 152°22'E), and (B) C. semilunata sp. nov. from Yelarbon State Forest, Queensland (28°32'S 151°06'E). Both recording were obtained in the field by LWP using RS1 (A), or RS2 (B) (see Methods and Terminology).
Figure 4 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 4. Map of central and eastern mainland Australia showing the geographical distribution of Clinopsalta adelaida
Figure 5 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 5. Clinopsalta semilunata sp. nov. (A) male holotype, Pratten (28.0912°S 151.7360°E) dorsal habitus; (B) male, ventral habitus; (C) female paratype, 6 km W of Thane (28°09'41"S 151°57'59"E) dorsal habitus.
Figure 2 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 2. Photos of male left timbals, with dorsal edge at top and posterior margin at right: (A) Clinopsalta autumna sp. nov., Narellan (31°18.14'S 149°02.05'E); (B) Clinopsalta semilunata sp. nov., Roma (26°33'S 148°47'E).
Figure 3 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 3. Clinopsalta autumna sp. nov., illustration of male pygofer and internal genitalia; (a) viewed laterally from the left; (b) viewed ventrally; (c) aedeagus, viewed laterally from left; and (d) apex of theca, viewed dorsally. Characters include: bpl, basal lobe of pygofer; cl, clasper; db, dorsal beak; ps, pseudoparameres; th, theca; un, uncus; upl, upper lobe of pygofer;vs, ventral support. Specimen from Narellan (31°18.14'S 149°02.05'E).
Figure 1 in Two New Species of Clinopsalta Moulds (Hemiptera: Cicadidae) and Additional Distribution Records for Clinopsalta adelaida (Ashton), with Notes on their Distinctive Calling Songs
Figure 1. Clinopsalta autumna sp. nov. (A) male, Narellan (31°18.14'S 149°02.05'E) dorsal habitus; (B) male, ventral habitus; (C) female, Narellan (31°18.14'S 149°02.05'E), dorsal habitus.
Data for: Zebra finch song ecology: monitoring of breeding, observational transects, focal and year-round acoustic recordings, and a large-scale simultaneous playback experiment
<p class="MsoNormal">Male songbirds sing to establish territories and to attract mates. However, increasing reports of singing in non-reproductive contexts and by females show that song use is more diverse than previously considered. Therefore, alternative functions of song, such as social cohesion and synchronisation of breeding, by and large were overlooked even in such well-studied species as the zebra finch (<em>Taeniopygia guttata</em>). In these social songbirds only the males sing and pairs breed synchronously in loose colonies following aseasonal rain events in their arid habitat. As males are not territorial, and pairs form long-term monogamous bonds early in life, conventional theory predicts that zebra finches should not sing much at all; yet they do and their song is the focus of hundreds of lab-based studies. We hypothesise that zebra finch song functions to maintain social cohesion and to synchronise breeding. Here we test this idea using data from five years of field studies, including observational transects, focal and year-round audio recordings, and a large-scale playback experiment. We show that zebra finches frequently sing while in groups, that breeding status influences song output at the nest and at aggregations, that they sing year-round, and that they predominantly sing when with their partner, suggesting that song remains important after pair formation. Our playback reveals that song actively features in social aggregations as it attracts conspecifics. Together, these results demonstrate that birdsong has important functions beyond territoriality and mate choice, illustrating its importance in coordination and cohesion of social units within larger societies.</p>
"I am a journalist myself, working for a public radio and television in the Netherlands. As a radio reporter Ivisited Bangladesh just after the cyclone Sidr hit the coastal area in November 1997 (…) Itravelled to the islands on a boat. On that boat were two boatmen and one of them started singing while we were sailing. As Igeotagged this song you can see exactly where it was. Iwas staying at that time in Pirojpur, took a taxi to the river and got a boat. Along tall typical motorboat. It was a journey of three-quarters of an hour during which he sang two songs." [Jeroen/zeshoog]12 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"I am a journalist myself, working for a public radio and television in the Netherlands. As a radio reporter Ivisited Bangladesh just after the cyclone Sidr hit the coastal area in November 1997 (…) Itravelled to the islands on a boat. On that boat were two boatmen and one of them started singing while we were sailing. As Igeotagged this song you can see exactly where it was. Iwas staying at that time in Pirojpur, took a taxi to the river and got a boat. Along tall typical motorboat. It was a journey of three-quarters of an hour during which he sang two songs." [Jeroen/zeshoog]12
Data for: Zebra finch song ecology: monitoring of breeding, observational transects, focal and year-round acoustic recordings, and a large-scale simultaneous playback experiment
Open the record for dataset details and reuse information.
Song recordings and annotation files of 3 canaries used to evaluate training of TweetyNet models for birdsong segmentation and annotation
<p>Many analyses of birdsong require time-consuming manual annotation of the individual elements of song, known as syllables or notes. We developed the first automated algorithm for birdsong annotation, "TweetyNet", that is applicable to complex song such as canary song. TweetyNet is trained with a small amount of hand-labeled data using supervised learning methods. We evaluate the amount of data required for training TweetyNet models using vocalizations of two songbird species - Bengalese finches and Canaries. This dataset contains song audio files and their accompanying annotation files for the three canaries used in this analysis.</p>
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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)
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DANDI Archive for NWB datasets
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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.