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99 results for “frog calls”

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dryad36/100

Frequency jumps and subharmonic components in calls of female Odorrana tormota differentially affect the vocal behaviors of male frogs

<p><span>Many studies have demonstrated that sounds containing nonlinear phenomena (NLP) can influence the behavior of receivers. However, the specific functions of different NLP components have received less attention. In most frog species, females produce few or no vocalizations; in contrast, female <em>O</em></span><span><em>dorrana</em> <em>tormota</em></span><span> exhibit a diverse range of calls that are rich in NLP components. Previous field playbacks have shown that female calls can elicit responses from male frogs. Therefore, we conducted a phonotaxis experiment to investigate the differential effects of different NLP calls by female <em>O. tormota</em> on the vocal behavior of male frogs. The results of our study revealed that calls with subharmonics elicited a greater number of short calls and answering calls from male frogs than calls with frequency jumps. Conversely, calls with frequency jumps triggered more staccato calls from males than calls with subharmonics. Additionally, during the phonotaxis experiments, we recorded the initial vocalizations of males in response to playbacks of female calls. The majority of males first produced short calls. Under calls with frequency jumps, most of the male frogs approaching within 10 cm of the loudspeaker produced staccato calls instead of "meow" calls or short calls. While under calls with subharmonics, most male frogs preferred to produce short calls. Our findings demonstrate that frequency jumps and subharmonic components in the calls of female <em>O. tormota</em> have different effects on male vocal behaviors.</span></p>

opencc-zeroDec 2022View details →
dryad36/100

Daily variation and repeatability of advertisement calls in an austral temperate forest frog under controlled conditions

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publicAug 2024View details →
dryad36/100

Túngara frog call-timing decisions arise as internal rhythms interact with fluctuating chorus noise

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publicApr 2024View details →
dryad36/100

Data for the detection of the boreal chorus frog (Pseudacris maculata) using environmental DNA and call surveys at 180 ponds sampled in 2017-2018 in southeastern Québec, Canada

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publicSep 2021View details →
dryad36/100

Sensory-motor tuning allows generic features of conspecific acoustic scenes to guide rapid, adaptive, call-timing responses in Túngara frogs

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publicAug 2024View details →
dryad36/100

Call attenuation data of three frog species in tree plantations and a native forest in southern Brazil

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publicJul 2023View details →
dryad36/100

Occurrence patterns and trends of frogs in coastal wetlands of the Great Lakes call for further habitat restoration

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publicMar 2025View details →
dryad36/100

Frequency jumps and subharmonic components in calls of female Odorrana tormota differentially affect the vocal behaviors of male frogs

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publicDec 2023View details →
dryad32/100

Allometric escape from acoustic constraints in frog calls is rare

<p class="AbstractSummary">Allometric constraint is a product of natural selection, particularly with respect to body size and traits constrained by physical properties thereof, such as metabolism, longevity, and vocal frequency. Parameters describing allometric relationships are conserved across most lineages, indicating that physical constraints dictate scaling patterns in deep time, despite substantial genetic and ecological divergence among organisms. Acoustic allometry (sound frequency ~ body size) is conserved across frogs, in defiance of massive variation in both body size and frequency. Here, we find four major instances of allometric escape, potentially deriving from ecomorphological adaptations to new signal modalities and invasion of biogeographic regions. In these instances of allometric escape, the optima and strength of the scaling relationship are different than expected for most other frog species, representing new adaptive regimes of body size ~ call frequency. Allometric constraints in frogs are highly conserved and have rarely promoted allometric escape despite frequent invasions of new adaptive regimes and dramatic ecomorphological divergence. Our results highlight instances in which natural and sexual selection combined could overcome physical constraints on sound production.</p>

opencc-zeroFeb 2021View details →
zenodo32/100

FIGURE 1 in The advertisement call of the rare casque-headed frog Nyctimantis galeata (Anura Hylidae) from its type locality, Morro do Chapéu, Bahia, Brazil

FIGURE 1. Advertisement call of Nyctimantis galeata from the municipality of Morro do Chapéu, state of Bahia, Brazil (air temperature 18–20ºC). A: Spectrogram and waveform of call (in the background noise calls of Proceratophrys redacta can be observed); B: Spectrogram, waveform and power spectrum of a note; C: Photograph of an adult N. galeata (MZUESC 21978, SVL = 4.43 cm).

opennotspecifiedSep 2020View details →
zenodo32/100

FIGURE 5. Call variation between Ameerega bassleri, A. pepperi and A in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru

FIGURE 5. Call variation between Ameerega bassleri, A. pepperi and A. yoshina. Box plots show period of silence between notes (L) and the calling rate (notes per minute) of the three species (R).

opennotspecifiedDec 2009View details →
zenodo32/100

FIGURE 6. Assa advertisement calls from A–B in A new hip-pocket frog from mid-eastern Australia (Anura: Myobatrachidae: Assa)

FIGURE 6. Assa advertisement calls from A–B) Assa wollumbin sp. nov. calls with nine and seven notes (Wollumbin, NSW) (Temperature 19.5 to 22.0 oC) (R.185956–60). (C–D) A. darlingtoni calls with 15 (Border Ranges National Park, NSW (Temperature 16 to 17.0 oC) and 13 (Conondale Ranges National Park, Qld. Temperature 18.2 oC). Waveforms (upper panel) display amplitude (y-axis) against time (x-axis, seconds); spectrograms (lower panel) display call frequency (y-axis) and intensity (degree of shading) against time (x-axis, seconds).

opennotspecifiedOct 2021View details →
dryad32/100

Female choice scores and Peak Frequency and Duration in calls from Wood frog chorus recordings

<p>A limitation in bioacoustic studies has been the inability to differentiate individual sonic contributions from group-level dynamics. We present a novel application of acoustic-camera technology to investigate how individual wood frogs calls influence chorus properties, and how variation influences mating opportunities. We recorded mating calls and used playback trials to gauge preference for different chorus types in the laboratory. Males and females preferred chorus playbacks with low variance in dominant frequency. Females preferred choruses with low mean peak frequency. Field studies revealed more egg masses laid in ponds where males chorused with low variance in dominant frequency. We also noted a trend towards more egg masses laid in ponds where males called with low mean frequency. Nearest neighbor distances influenced call timing (neighbors called in succession) and distances increased with variance in chorus frequency. Results highlight the potential fitness implications of individual-level contributions to a bioacoustic signal produced by groups.</p>

opencc-zeroFeb 2022View details →
zenodo32/100

FIGURE 12 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 12. Advertisement call of Mannophryne herminae. Oscillogram (a) and spectrogram (b) of a 5 s fragment of the call. Detailed view of the oscillogram (c) and spectrogram (d) of a 1 s section of the same recording.

opennotspecifiedAug 2018View details →
zenodo32/100

FIGURE 8 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 8. César Ramón Molina Rodriguez (1960–2015) with an amplectant couple of the critically endangered Rancho Grande Harlequin Frog Atelopus cruciger in January 2010. We named Mannophryne molinai sp. nov. after him in a posthumous recognition of his friendship and contributions to the knowledge of the diversity and conservation of Venezuelan amphibians and reptiles. Photo: F.J.M. Rojas-Runjaic.

opennotspecifiedAug 2018View details →
zenodo32/100

FIGURE 11 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 11. Live specimens of Mannophryne herminae from San Esteban River, Carabobo state, Venezuela (near the type locality). Adult female, dorsolateral (a) and ventral (b) views; adult male, dorsolateral (c) and ventral (d) views. Photos: F.J.M. Rojas-Runjaic.

opennotspecifiedAug 2018View details →
zenodo32/100

FIGURE 10 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 10. Dorsal (a) and ventral (b) views of the type series of Mannophryne herminae. 1. Lectotype male SMF 7286; Paralectotypes SMF 7316 (2, female), SMF 7317 (3, male); SMF 7318 (4, male); SMF 7319 (5, female); SMF 54898 (6, female); SMF 54899 (7, female). (c) Label with catalog information of the paralectotypes. Photos: S. Lotzkat.

opennotspecifiedAug 2018View details →
zenodo32/100

FIGURE 7 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 7. La Rondona creek, Sierra de Aroa, northwestern Venezuela, type locality of Mannophryne molinai sp. nov. (a) View of a small pool and (b) crevices below a waterfall were several specimens of the type series were found. Photos: F.J.M. Rojas-Runjaic.

opennotspecifiedAug 2018View details →
zenodo32/100

FIGURE 5 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 5. Ventral view of four preserved paratypes of Mannophryne molinai sp. nov. showing variation in the dark dermal collar. Paratype females MHNLS 21337 (a), and MHNLS 21535 (b); paratype males MHNLS 21537 (c), and MHNLS 21538 (d). Fotos: F.J.M. Rojas-Runjaic

opennotspecifiedAug 2018View details →
zenodo32/100

FIGURE 3 in Unveiling species diversity in collared frogs through morphological and bioacoustic evidence: a new Mannophryne (Amphibia, Aromobatidae) from Sierra de Aroa, northwestern Venezuela, and an amended definition and call description of M. herminae (Boettger, 1893)

FIGURE 3. Map of northern Venezuela, and Trinidad and Tobago, indicating the type localities of the 20 known species of Mannophryne: 1. M. molinai sp. nov.; 2. M. caquetio; 3. M. collaris; 4. M. cordilleriana; 5. M. herminae; 6. M. lamarcai; 7. M. larandina; 8. M. leonardoi; 9. M. neblina; 10. M. oblitterata; 11. M. olmonae; 12. M. orellana; 13. M. riveroi; 14. M. speeri; 15. M. trinitatis; 16. M. trujillensis; 17. M. urticans; 18. M. venezuelensis; 19. M. vulcano; 20. M. yustizi.

opennotspecifiedAug 2018View details →

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International Brain Laboratory public data

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