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99 results for “frog calls”

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zenodo28/100

Figure 1 from: Dias IR, Mira-Mendes CV, Souza-Costa CA, Juncá FA, Solé M (2017) The advertisement call and comments on the distribution of Eleutherodactylus bilineatus Bokermann, 1975, an endemic frog of Bahia State, Brazil (Amphibia, Anura). ZooKeys 677: 151-159. https://doi.org/10.3897/zookeys.677.12309

Figure 1 - Different individuals of Eleutherodactylus bilineatus showing some variation of the dorsal pattern of the species. A and B RPPN Mata do Passarinho, Macarani C Estação Ecológica Wenceslau Guimarães and D Serra do Corcovado, Almadina, Bahia, Brazil (photographs A, B and D Iuri R. Dias, C Rafael O. Abreu).

opencc-by-4.0May 2017View details →
zenodo28/100

Figure 3 from: Dias IR, Mira-Mendes CV, Souza-Costa CA, Juncá FA, Solé M (2017) The advertisement call and comments on the distribution of Eleutherodactylus bilineatus Bokermann, 1975, an endemic frog of Bahia State, Brazil (Amphibia, Anura). ZooKeys 677: 151-159. https://doi.org/10.3897/zookeys.677.12309

Figure 3 - Advertisement call of Eleutherodactylus bilineatus (MZFS 600). (A) Waveform and (B) audiospectrogram. Recorded on April 21, 1997 at 20h 50min. Air temperature during recording 20° C.

opencc-by-4.0May 2017View details →
zenodo28/100

Figure 2 from: Dias IR, Mira-Mendes CV, Souza-Costa CA, Juncá FA, Solé M (2017) The advertisement call and comments on the distribution of Eleutherodactylus bilineatus Bokermann, 1975, an endemic frog of Bahia State, Brazil (Amphibia, Anura). ZooKeys 677: 151-159. https://doi.org/10.3897/zookeys.677.12309

Figure 2 - Distribution map of known localities for Eleutherodactylus bilineatus. Key: black star = type locality; red circle = new records; black circles = literature records. Municipalities = 1 Santa Teresinha 2 Amargosa 3 Wenceslau Guimarães 4 Valença 5 Cairu 6 Nilo Peçanha 7 Igrapiúna 8 Jequié 9 Boa Nova 10 Almadina 11 Barro Preto 12 Uruçuca 13 Ilhéus (Type Locality) 14 Jussari 15 Arataca, 16 Camacan 17 Canavieiras 18 Itarantim 19 Macarani and 20 Guaratinga. BA = state of Bahia; MG = state of Minas Gerais and ES = state of Espírito Santo. More details of the records are present in Table 1.

opencc-by-4.0May 2017View details →
zenodo28/100

Figure 2 from: Luna-Dias C, Carvalho-e-Silva SP (2019) Calls of Boana latistriata (Caramaschi & Cruz, 2004) (Amphibia, Anura, Hylidae), an endemic tree frog from the State of Minas Gerais, Brazil. ZooKeys 820: 83-94. https://doi.org/10.3897/zookeys.820.30711

Figure 2 Calls of Boanalatistriata from its type locality. Two examples of call A, emitted by the individual ZUFRJ 15077 (snout-vent length = 40.0 mm), showing the last pulses fused in a pulsatile (below the red lines).

opencc-by-4.0Feb 2019View details →
zenodo28/100

Figure 1 from: Luna-Dias C, Carvalho-e-Silva SP (2019) Calls of Boana latistriata (Caramaschi & Cruz, 2004) (Amphibia, Anura, Hylidae), an endemic tree frog from the State of Minas Gerais, Brazil. ZooKeys 820: 83-94. https://doi.org/10.3897/zookeys.820.30711

Figure 1 Calls of Boanalatistriata from its type locality. A Waveform and B spectrogram showing three instances of call A and one of call B emitted in sequence C waveform and D spectrogram of a call A, in detail, indicating seven visible harmonics numbered I to VII E waveform and F spectrogram of a call B, in detail. Images were obtained using Raven Pro 1.5 software. Spectrograms parameters: window type = Hann, size = 256 samples, overlap = 99%. Individual ZUFRJ 15076 (snout-vent length = 39.3 mm), recorded at a temperature between 12 and 14 °C.

opencc-by-4.0Feb 2019View details →
zenodo28/100

Figure 1 in Vocalizations of the Brazilian torrent frog Hylodes heyeri (Anura: Hylodidae): Repertoire and influence of air temperature on advertisement call variation

Figure 1. Advertisement call of Hylodes heyeri from the Municipality of Morretes, Parana´, Brazil. Recorded on 8 April 2002, at 21.7°C. (A) Power spectrum; (B) spectrogram; (C) oscillogram.

opencc-by-4.0Jul 2010View details →
zenodo28/100

F in Advertisement calls of Neotropical poison frogs (Amphibia: Dendrobatidae) of the genera Colostethus, Dendrobates and Epipedobates, with notes on dendrobatid call classification

F. 1. Oscillogram and audiospectrogram of the advertisement call of Colostethus brunneus.

opennotspecifiedAug 2003View details →
zenodo28/100

Figure 4 in The advertisement call and tadpole of the Ambangulu Puddle Frog (Phrynobatrachus ambanguluensis) (Anura: Phrynobatrachidae) from Tanzania

Figure 4. Mouthparts of Phrynobatrachus ambanguluensis.

opennotspecifiedApr 2021View details →
zenodo28/100

Figure 3. A Phrynobatrachus ambanguluensis tadpole, PEM A14286 in The advertisement call and tadpole of the Ambangulu Puddle Frog (Phrynobatrachus ambanguluensis) (Anura: Phrynobatrachidae) from Tanzania

Figure 3. A Phrynobatrachus ambanguluensis tadpole, PEM A14286. Scale bar = 10 mm.

opennotspecifiedApr 2021View details →
zenodo28/100

Figure 2 in The advertisement call and tadpole of the Ambangulu Puddle Frog (Phrynobatrachus ambanguluensis) (Anura: Phrynobatrachidae) from Tanzania

Figure 2. Advertisement call of Phrynobatrachus ambanguluensis. Waveform above, spectrogram below.

opennotspecifiedApr 2021View details →
zenodo28/100

1 in Intraspecific Call Variation in the Mimic Poison Frog Ranitomeya imitator

1+ tanh 2x ae ‾c ŋ= +ŋ min 2 ŋ max ‾ 1 ŋmin

opennotspecifiedDec 2015View details →
dryad28/100

Multisensory integration facilitates perceptual restoration of an interrupted call in frog

Open the record for dataset details and reuse information.

publicMar 2022View details →
dryad24/100

Data from: Males increase call frequency, not intensity, in response to noise, revealing no Lombard effect in the little torrent frog

Noise is one of the main factors that can influence the processes of sound communication across a wide range of animal groups. Although the effects of ambient noise on animal communication, including anthropogenic noise, have received increasing attention, few studies have examined changes in the fine structure of acoustic signals produced by vocalizing species in constantly noisy environments. Here, we used natural recordings to determine the associations between stream noise and call parameters in the little torrent frog (Amolops torrentis). We also used playbacks of stream noise recorded in natural habitats and playbacks of white noise to examine how male vocal signals change with increasing noise levels. The results show that noise intensity has a significant effect on male call frequency, but not on call amplitude or other call characteristics. Based on this evidence, we suggest that in streamside species stream noise drives males to alter call frequency and call as loudly as possible in order to improve discriminability. These findings provide insights into the role played by ecological selection in the evolution of noise‐dependent anuran vocal plasticity

opencc-zeroDec 2017View details →
dryad24/100

Data from: Males increase call frequency, not intensity, in response to noise, revealing no Lombard effect in the little torrent frog

Open the record for dataset details and reuse information.

publicNov 2018View details →
zenodo20/100

FIGURE 2. One advertisement call with 47 in The tadpole of the hylodid frog Hylodes ornatus (Bokermann, 1967), including chondrocranium description, and advertisement call

FIGURE 2. One advertisement call with 47 notes of Hylodes ornatus (MNRJ 33405) form Parque Nacional do Itatiaia, municipality of Itamonte, Minas Gerais, Brazil. A: oscilogram; B: sonogram; C: power spectrum.

opennotspecifiedMar 2012View details →
zenodo20/100

Figure 2 in Advertisement call, tadpole morphology, and other natural history aspects of the threatened poison frog Andinobates daleswansoni (Dendrobatidae)

Figure 2. Aerial image of the Selva de Florencia National Natural Park (shadow brown area) and its location in the Central Andes of Colombia. Red square represents the site where the study was conducted. The red dots represent historical records of A. daleswansoni (Rueda-Almonacid et al. 2006; Brown et al. 2011; Duarte-Marín et al. 2018), and the red star represents the type locality of the species ('El Estadero', Municipality of Florencia, Caldas). The orange dots indicate records for Andinobates opisthomelas, a morphological similar species to A. daleswansoni (Ruiz-Carranza et al. 1996; Brown et al. 2011). Note that this study was performed in the municipality of Pensilvania, where A. opisthomelas has not been recorded.

opennotspecifiedMay 2021View details →
zenodo20/100

Figure 6 in Advertisement call, tadpole morphology, and other natural history aspects of the threatened poison frog Andinobates daleswansoni (Dendrobatidae)

Figure 6. Images of the oral disc (a, b), vent tube or spiracle (c), and limb buds of the tadpole of Andinobates daleswansoni (Gosner Stage 26). Scale bar = 1.0 mm. Voucher at the Colección de Anfibios y Reptiles of the Biology programme at the Universidad del Quindío, Armenia, Colombia: ARUQ-978. Black arrow shows the gap in the marginal papillae.

opennotspecifiedMay 2021View details →
zenodo20/100

FIG. 4 in Intraspecific Call Variation in the Mimic Poison Frog Ranitomeya imitator

FIG. 4.—Boxplots comparing call parameters between the striped morph (open boxes) and varadero morph (shaded boxes) at the striped-varadero transition zone. Asterisks indicate differences in call parameters between mimetic morphs of Ranitomeŋa imitator.

opennotspecifiedDec 2015View details →
zenodo20/100

Figure 1 in Quantification of underwater calling and foraging activities in the African clawed frog Xenopus laevis

Figure 1. Circadian variation of the probability of call detection in Xenopus laevis (solid line). Standard errors of the mean are indicated as dotted lines. The lines highlighting the diel variation has been computed using a polynomial regression.

opennotspecifiedOct 2022View details →

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Last verified 2026-04-29Open record