@article {58461, title = {Acoustic radiation patterns of mating calls of the t{\'u}ngara frog (Physalaemus pustuosus): Implications for multiple receivers}, volume = {126}, year = {2009}, month = {Nov-01-2009}, pages = {2757-2767}, abstract = {

In order for a signal to be transmitted from a sender to a receiver, the receiver must be within theactive space of the signal. If patterns of sound radiation are not omnidirectional, the position as wellas the distance of the receiver relative to the sender is critical. In previous measurements of thehorizontal directivity of mating calls of frogs, the signals were analyzed using peak orroot-mean-square analysis and resulted in broadband directivities that ranged from negligible to amaximum of approximately 5 dB. Idealized laboratory measurements of the patterns of acousticradiation of the mating calls of male t\úngara frogs\ Physalaemus pustulosus, along axes relevant tothree receivers in this communication network, female frogs in the horizontal plane, and frog-eatingbats and blood-sucking flies above the ground, are reported. The highest sound pressure level wasradiated directly above the frog, with a 6 dB reduction radiated along the horizontal direction.Band-limited directivities were significantly greater than broadband directivities, with a maximumdirectivity of 20 dB in the vertical plane for harmonics near 6 kHz. The implications with regard tomating and predator-prey interactions are discussed.

}, issn = {0001-4966}, doi = {10.1121/1.3212929}, url = {http://dx.doi.org/10.1121/1.3212929}, author = {Bernal, Ximena E. and Page, Rachel A. and Ryan, Michael J. and Argo, Theodore F. and Wilson, Preston S.} } @article {58416, title = {Vocalization of the Sullen toad, Scythrophrys sawayae (Anura: Leptodactylidae: Paratelmatobiinae), from near its type locality, Paran{\'a}, Brazil}, journal = {Salamandra}, volume = {57}, year = {2021}, pages = {167-170}, chapter = {167}, author = {Camila F. Moser and Rodrigo Lingnau} } @article {58252, title = {Description of the Advertisement and Aggressive Calls of the Enigmatic Trinidad Thin-Toed Frog Leptodactylus nesiotus}, journal = {South American Journal of Herpetology}, volume = {15}, year = {2020}, month = {Jan-04-2020}, pages = {63}, abstract = {

Research on elusive amphibians is challenging, resulting in a lack of basic information on their natural history. This is the case of Leptodactylus nesiotus, a rare and elusive frog found in a small swamp in the southwestern peninsula of the island of Trinidad (West Indies). Here, we provide additional call descriptions for data collected in the field (Trinidad) and laboratory in 2004, including descriptions of both advertisement and aggressive calls. The notes in the advertisement calls were divided in two types of pulses, both lasting on average less than 0.04 s and with average peak frequencies less than 16,000 Hz. The aggressive calls also displayed two types of pulses lasting 0.06 s maximum on average and with highest average peak frequency of 1,612 Hz. The only significant difference between these two call types relates to the temporal structures, but a larger dataset is needed to confirm the pattern. There were no temporal significant differences between the calls described here and the ones described in earlier literature, although we provide a more detailed call description.

}, doi = {10.2994/SAJH-D-18-00011.1}, url = {https://bioone.org/journals/south-american-journal-of-herpetology/volume-15/issue-1/SAJH-D-18-00011.1/Description-of-the-Advertisement-and-Aggressive-Calls-of-the-Enigmatic/10.2994/SAJH-D-18-00011.1.full}, author = {Borz{\'e}e, Ama{\"e}l and Nguyen, Hoa Quynh and Jowers, Michael J.} } @article {57997, title = {Variation in Bioacoustic Characteristics in Eleutherodactylus coqui Thomas, 1966 and Eleutherodactylus antillensis (Reinhardt and Lutken, 1863) (Anura: Eleutherodactylidae) in the Puerto Rico Bank}, year = {2019}, abstract = {

Bioacoustics is an interdisciplinary science that combines biology, acoustics, and mathematics. This discipline can be used to study population ecology and behavior. Furthermore, we can use this tool to assess a population and suggest if a species of interest may be in a transitional state of becoming a new species by allopatric speciation. Amphibians communicate via sound and the environment has a key role in metabolism and sound dispersion. By analyzing temporal and spectral properties of acoustical communication in anurans, we can understand better how these animals are evolving to cope with their ever-changing environment. We studied the variation in acoustic parameters among five populations each of the red-eye coqui, Eleutherodactylus antillensis (Reinhardt and Lutken, 1863) and the common coqui, E. coqui Thomas, 1966 across the Puerto Rico Bank. These species are changing their vocalizations. Some populations have higher sound frequencies than other conspecific populations; other nocturnal species have populations with different temporal patterns of sound production. We found strong variation among the five populations examined for each species. In, E. antillensis, the size of the organism relates to temporal variation in sound production (i.e., inter-note interval and total call duration) and did not relate to spectral differentiation. In E. coqui, the population living at highest elevation above sea level assessed had a spectral footprint no other population shares, probably due to geographic isolation from other conspecific populations that live in lower elevations.

}, keywords = {bioacoustics, communication, Eleutherodactylus, Eleutherodactylus antillensis, Eleutherodactylus coqui, microevolution, Puerto Rico, sound spectrogram, speciation}, doi = {10.9784/LEB7(2)Rios.01}, author = {Alejandro R{\'\i}os-Franceschi and Rafael L. Joglar and Richard Thomas} } @article {57911, title = {On the Uncertain Taxonomic Identity of Adenomera hylaedactyla (Cope, 1868) and the Composite Type Series of A. andreae (M{\"u}ller, 1923) (Anura, Leptodactylidae)}, journal = {Copeia}, volume = {107}, year = {2019}, month = {Jan-11-2019}, pages = {708}, abstract = {

Adenomera andreae and A. hylaedactyla are two widespread Amazonian frogs that have been traditionally distinguished from each other by the use of different habitats, toe tip development, and more recently through advertisement calls. Yet, taxonomic identification of these species has always been challenging. Herein we undertake a review of type specimens and include new phenotypic (morphology and vocalization) and mitochondrial DNA information for an updated diagnosis of both species. Our morphological analysis indicates that the single type (holotype) of A. hylaedactyla could either belong to lineages associated with Amazonian forest-dwelling species (A. andreae clade) or to the open-formation morphotype (A. hylaedactyla clade). Given the holotype\&$\#$39;s poor preservation, leading to the ambiguous assignment of character states for toe tip development, as well as a vague type locality encompassing a vast area in eastern Ecuador and northern Peru, the identity of this specimen is uncertain. Morphology of toe tip fragments and the original species description suggest that A. hylaedactyla could correspond to at least two described species (A. andreae or A. simonstuarti) or additional unnamed genetic lineages of the A. andreae clade, all bearing toe tips expanded into discs. Analysis of morphometric data, however, clustered the holotype with the Amazonian open-formation morphotype (toe tips unexpanded). While additional data can be obtained from the holotype of A. hylaedactyla, at this time this type cannot be unequivocally assigned to any species of Adenomera distributed across eastern Ecuador and Peru\&$\#$39;s northernmost region of Loreto. For the time being, the name A. hylaedactyla still accommodates the only Amazonian open-habitat species. As to the type series of Adenomera andreae, a forest-associated species with toe tips fully expanded (developed into small discs) from eastern Brazilian Amazonia, we found that one of its paratypes shares a morphotype with the open-habitat species and is reassigned to A. hylaedactyla. With the taxonomic identity of A. hylaedactyla unresolved, formal descriptions of cryptic species complexes within the A. andreae clade distributed across the type locality of A. hylaedactyla run the risk of a possible future synonymization with A. hylaedactyla. Yet, not naming more circumscribed and potentially threatened cryptic species puts them at risk, as they would probably not qualify for conservation funding. Given the current fire crisis in the Amazon Basin, the risk of losing species before they are described far outweighs the risk of synonymization. We recommend that researchers prioritize descriptions based on the potential extinction risk of new species.

}, doi = {10.1643/CH-19-237}, url = {https://bioone.org/journals/copeia/volume-107/issue-4/CH-19-237/On-the-Uncertain-Taxonomic-Identity-of-Adenomera-hylaedactyla-Cope-1868/10.1643/CH-19-237.full}, author = {Thiago R. De Carvalho and Giaretta, Ariovaldo A. and Maciel, Natan M. and Barrera, Diego A. and Aguilar-Puntriano, C{\'e}sar and Haddad, C{\'e}lio F. B. and Marcelo N. C. Kokubum and Menin, Marcelo and Angulo, Ariadne} } @article {57662, title = {A New Cryptic Species of the Adenomera andreae Clade from Southwestern Amazonia (Anura, Leptodactylidae)}, journal = {Herpetologica}, volume = {75}, year = {2019}, month = {Jan-09-2019}, pages = {233}, abstract = {

We describe a new Amazonian species of Adenomera that corresponds to one of the acoustic signals and morphs from Tambopata National Reserve (Adenomera \‘\‘Forest Call I\’\’) and to a confirmed candidate species (Adenomera sp. E) in the most recently published phylogeny for the genus. The new species is distinguished from all 19 described congeners by its unique advertisement call, consisting of a single multipulsed note, formed by 22\–35 partly fused pulses (greatest pulse number recorded for the genus among species with partly fused notes). The new species is further distinguished from most congeners in having toe tips expanded into small discs. Its distribution is associated with the Amazonian region encompassing western Brazil (state of Acre), southeastern Peru, and north-central Bolivia.

}, keywords = {Amazon rain forest, bioacoustics, biodiversity, integrative taxonomy, Leptodactylinae, Tambopata}, doi = {10.1655/D-18-00049}, url = {https://bioone.org/journals/herpetologica/volume-75/issue-3/D-18-00049/A-New-Cryptic-Species-of-the-Adenomera-andreae-Clade-from/10.1655/D-18-00049.full}, author = {Thiago R. De Carvalho and Angulo, Ariadne and Marcelo N. C. Kokubum and Barrera, Diego A. and De Souza, Mois{\'e}s B. and C{\'e}lio F. B. Haddad and Ariovaldo A. Giaretta} } @article {57646, title = {A new frog of the Leptodactylus fuscus species group (Anura: Leptodactylidae), endemic from the South American Gran Chaco}, journal = {PeerJ}, volume = {7}, year = {2019}, month = {Jan-01-2019}, pages = {e7869}, doi = {10.7717/peerj.7869}, url = {https://peerj.com/articles/7869}, author = {Schneider, Rosio G. and Dario E. Cardozo and Brusquetti, Francisco and Kolenc, Francisco and Borteiro, Claudio and C{\'e}lio F. B. Haddad and Basso, Nestor G. and Baldo, Diego} } @article {57579, title = {Seasonal variation in abundance and diversity of eavesdropping frog-biting midges (Diptera, Corethrellidae) in a neotropical rainforest}, year = {2018}, abstract = {

In the tropics, precipitation patterns result in seasonal fluctuations in the abundance and distribution of plant and animal species. Tropical predators and parasites are therefore faced with seasonal changes in prey and host availability.
2. This study investigates the seasonal interaction among a specialised ectoparasite, eavesdropping frog-biting midges (Corethrella spp.), and their anuran hosts, examining how the abundance and diversity of the frog-biting midge community fluctuate between the rainy (host abundant) and dry (host sparse) seasons.
3. Midges were captured in both the rainy and dry seasons using acoustic playbacks of calls from a common frog species that breeds during the rainy season, the t\úngara frog (Engystomops, Physalaemus, pustulosus). During the dry season t\úngara frog choruses are absent. To explore seasonal shifts in host preference or changes in the midge community due to host specificity, midges were also captured using playbacks of calls from a frog that breeds during the dry season, the pug-nosed tree frog (Smilisca sila).
4. While the overall abundance of midges decreased in the dry season, only slight differences in the relative abundance between midge species were found. These results suggest that midge populations can shift between hosts as they become available across seasons, allowing adult populations of frog-biting midges to persist year-round. To overcome the challenge of detecting and localising different host species, it is proposed that frog-biting midges have evolved a generalised acoustic template, allowing them to respond to a broad range of available hosts, regardless of seasonal host composition.

}, keywords = {Corethrella, Engystomops pustulosus, frog-biting midges, phenology, Smilisca sila, tropical seasonality}, doi = {10.1111/een.12492}, url = {http://doi.wiley.com/10.1111/een.12492}, author = {Legett, Henry D. and BARANOV, VIKTOR A. and Ximena E. Bernal} } @inbook {57555, title = {Be loved, be prey, be eaten}, year = {2014}, abstract = {

Animal communication is one of the most fundamental of all social behaviors. It modulates interactions among neighbors and strangers, siblings and parents, and individuals and their prospective mates. One of the most fundamental functions of communication is to enhance the sender\’s conspicuousness, to cause the sender to stand out against the background so it can be detected by the receiver. This is a challenge for signals that function over long distances, such as those that function in territorial advertisement and mate attraction, because signal intensity and fidelity decrease with distance from the sender. At longer distances a signal is less likely to be above the receiver\’s threshold for detection and recognition, and it is also more likely to be masked by noise as the intensity of noise at the receiver is independent of its distance from the sender.

Another type of noise is generated by conspecifics signaling in the same channel. We may perceive a chorus of frogs or insects as a melodious, even co- operative unit. But to members of the chorus the calls of their neighbors are every bit as deleterious to their own call\’s ability to be detected as is environ- mental noise. There is also \“noise\” within the perceptual systems of the receiver that ameliorates signal detection. One example is habituation. Upon continual exposure to a signal, an animal will tend to ignore it, and some of the animal\’s neurons will cease to fire. Another type of perceptual noise is incremental forgetting of a signal once it is perceived. Some signals are more\ memorable than others, surviving longer in the receiver\’s memory. The importance of conspecific noise and perceptual noise is usually less appreciated in animal communication studies than is environmental noise.

Selection often will favor senders to produce communication signals that stand out against these three types of background noise. Conspicuousness is accomplished in a variety of ways. In the acoustic domain animals can use fre- quency bands that contain less noise; they can call longer, at a faster rate, or at a higher amplitude; they can call during periods when others are silent; and they can produce calls that are more complex. Visual signals can stand out more against background when their spectral properties and spatial patterns differ from those in the background, when colors are brighter and patterns are more complex, and when motion patterns associated with the signal, such as push-up displays in lizards, are different than the pattern of background movement, such as vegetation being blow in the wind (e.g., Fleishman, 1992). Increasing signal complexity in both the acoustic and visual domains can to some extent remedy the receiver habituating to and forgetting a signal. There is less known about how chemical, tactile, and electrical signals can enhance contrast with the background.

In a survey of preferences for sexual signals, Michael Ryan and Anne Keddy-Hector (1992) showed that across modalities prospective mates tended to prefer sexual signals that were greater in magnitude: longer and louder, faster and brighter, more complex and with more background contrast. Although there were numerous cases in which prospective mates preferred signals that were near the population mean, there were few cases in which there was a preference for signals of lesser magnitude. A simple rule of thumb for sexual signals is that more is better. Selection for signal efficacy, however, creates a dilemma for the sender: the curse of unintended receivers. In general, each signal has evolved under selection to communi- cate with a specific intended receiver. In the case of sexual advertisement sig- nals, the intended receivers are prospective mates, usually female conspecifics. Other receivers can also detect and respond to signals even if there was no selection on the sender to communicate with them. We refer to these receivers as eavesdroppers or unintended receivers. It is important to note that the terms intended and unintended should not imply intention- ality but instead refer to hypotheses about the selection forces that favored the evolution of these signals. With few exceptions, senders and receivers do not communicate in a private channel. The world is populated by unin- tended receivers, eavesdroppers who are attendant to the signals of senders, often to the demise of senders. In this chapter we explore the tension that exists in sexual communication systems between being conspicuous to\ potential mates and attracting eavesdroppers, between being loved, being prey, and being eaten.

}, author = {Rachel A. Page and Michael J. Ryan and Ximena E. Bernal} } @article {57551, title = {Synchronized mating signals in a communication network: the challenge of avoiding predators while attracting mates}, year = {2019}, abstract = {

Conspicuous mating signals attract mates but also expose signallers to predators and parasites. Signal evolution, therefore, is driven by conflicting selective pressures from multiple receivers, both target and non-target. Synchronization of mating signals, for example, is an evolutionary puzzle, given the assumed high cost of reduced female attraction when signals over- lap. Synchronization may be beneficial, however, if overlapping signals reduce attraction of non-target receivers. We investigate how signal synchro- nization is shaped by the trade-off between natural and sexual selection in two anuran species: pug-nosed tree frogs (Smilisca sila), in which males pro- duce mating calls in near-perfect synchrony, and t\úngara frogs (Engystomops pustulosus), in which males alternate their calls. To examine the trade-off imposed by signal synchronization, we conducted field and laboratory play- back experiments on eavesdropping enemies (bats and midges) and target receivers (female frogs). Our results suggest that, while synchronization can be a general strategy for signallers to reduce their exposure to eavesdrop- pers, relaxed selection by females for unsynchronized calls is key to the evolution and maintenance of signal synchrony. This study highlights the role of relaxed selection in our understanding of the origin of mating signals and displays.

}, keywords = {acoustic communication, communication network, eavesdroppers, relaxed selection, synchrony}, doi = {10.1098/rspb.2019.1067}, url = {https://royalsocietypublishing.org/doi/10.1098/rspb.2019.1067}, author = {Legett, Henry D. and Rachel A. Page and Ximena E. Bernal} } @article {57357, title = {Harmonics: Rediscovering Eleutherodactylus Vocalizations}, journal = {Life: The Excitement of Biology}, volume = {5}, year = {2018}, chapter = {173}, abstract = {

There are 17 described species of Eleutherodactylus in Puerto Rico, some more common than others. The use of harmonics as a means of vocalization has been little studied in the Caribbean. As part of a long-term study of the evolution of sonic communication in Puerto Rican Eleutherodactylus frogs, we document the use harmonics in three common but distinct Puerto Rican endemic species: E. coqui, E. antillensis, and E. brittoni. This study focuses only on the description of these vocalizations using computer software not on the behavioral implications of these vocalizations.

}, keywords = {Eleutherodactylus, harmonics, Puerto Rico, vocalizations}, doi = {10.9784/LEB5(4)Rios.01}, author = {Alejandro R{\'\i}os-Franceschi and Rafael L. Joglar} } @article {53584, title = {Environmental constraints on size-dependent signaling affects mating and rival interactions}, journal = {Behavioral Ecology}, year = {2019}, month = {Mar-02-2020}, abstract = {

Advertisement signals can convey information about a sender\’s characteristics, such as body size. The reliability of signals, however, can be reduced when signal production is partially dependent on the environment. Here, we assess the effect of display-site properties on the production, attractiveness and honesty of sexual signals. We recorded male t\úngara frogs (Physalaemus pustulosus) while manipulating water levels in order to constrain calling. We found that water level affected male call properties in a size-dependent manner, with call amplitude being less affected in smaller males when forced to call in shallow water. Next, we tested how size-dependent and display-site-dependent signaling affected female choice and rival competition. Both males and females showed the strongest response to the call of a large male when he was calling at the deepest water levels. However, females showed no preference for large over small males when both were recorded in shallow water levels, or, depending on the call rate and timing of calls, even preferred small males. Likewise, males responded equally to large and small rivals recorded calling during shallow water level trials. Our experiments show that display-site properties can influence signal production and attractiveness in a size-dependent manner. These results can have important consequences for the evolution of signaling, as small males may be able to use their size to their advantage when selecting appropriate display sites and thereby outcompete large males.

}, keywords = {display site, honest signaling, Physalaemus pustulosus, production constraints, sexual selection}, issn = {1045-2249}, doi = {10.1093/beheco/arz009}, url = {https://academic.oup.com/beheco/advance-article/doi/10.1093/beheco/arz009/5320523}, author = {Smit, Judith A H and Loning, Hugo and Halfwerk, Wouter} } @article {53414, title = {Behavioral and neural auditory thresholds in a frog}, journal = {Current Zoology}, year = {2018}, abstract = {

Vocalizations play a critical role in mate recognition and mate choice in a number of taxa, especially, but not limited to, orthopterans, frogs, and birds. But receivers can only recognize and prefer sounds that they can hear. Thus a fundamental question linking neurobiology and sexual selection asks\— what is the threshold for detecting acoustic sexual displays? In this study we use three methods to assess such thresholds in t\úngara frogs: behavioral responses, auditory brainstem responses, and multi-unit electrophysiological recordings from the midbrain. We show that thresholds are lowest for multi-unit recordings (ca. 45 dB SPL), and then for behavioral responses (ca. 61 dB SPL), with auditory brainstem responses exhibiting the highest thresholds (ca. 71 dB SPL). We discuss why these estimates differ and why, as with other studies, it is unlikely that they should be the same. Although all of these studies estimate thresholds they are not measuring the same thresholds; behavioral thresholds are based on signal salience while the two neural assays estimate physiological thresholds. All three estimates, however, make it clear that to have an appreciation for detection and salience of acoustic signals we must listen to those signals through the ears of the receivers.

}, keywords = {anurans, auditory brainstem responses, auditory thresholds, mate choice, Physalaemus pustulosus, sexual selection, signal recognition thresholds, t{\'u}ngara frogs, vocalizations}, author = {Ryan, C and Akre, Karin and Wilczynski, Walter and others} } @article {52575, title = {Interactions between complex multisensory signal components result in unexpected mate choice responses}, journal = {Animal Behaviour}, volume = {134}, year = {2017}, month = {Jan-12-2017}, pages = {239 - 247}, abstract = {

Multimodal (multisensory) signalling is common in many species and often facilitates communication. How receivers integrate individual signal components of multisensory displays, especially with regard to variance in signal complexity, has received relatively little attention. In nature, male t\úngara frogs, Physalaemus pustulosus, produce multisensory courtship signals by vocalizing and presenting their inflating and deflating vocal sac as a visual cue. Males can produce a simple call (whine only) or a complex call (whine \þ one or more chucks). In a series of two-choice experiments, we tested female preferences for variation in acoustic call complexity and amplitude (unimodal signals). We then tested preferences for the same calls when a dynamic robotic frog was added to one call, generating a multi- modal stimulus. Females preferred a complex call to a simple call; when both calls contained at least one chuck, additional numbers of chucks did not further increase attractiveness. When calls contained zero or one chuck, the visual stimulus of the robofrog increased call attractiveness. When calls contained multiple chucks, however, the visual component failed to enhance call attractiveness. Females also preferred higher amplitude calls and the addition of the visual component to a lower amplitude call did not alter this preference. At relatively small amplitude differences, however, the visual signal increased overall discrimination between the calls. These results indicate that the visual signal component does not provide simple enhancement of call attractiveness. Instead, females integrate multisensory components in a nonlinear fashion. The resulting perception and behavioural response to complex signals probably evolved in response to animals that communicate in noisy environments.

}, keywords = {anurans, mate choice, multimodal signalling, nonlinear interactions, sexual selection, signal weighting, t{\'u}ngara frog, vocal sac}, issn = {00033472}, doi = {10.1016/j.anbehav.2016.07.005}, url = {http://linkinghub.elsevier.com/retrieve/pii/S000334721630121X}, author = {Stange, Nicole and Rachel A. Page and Michael J. Ryan and Taylor, Ryan C.} } @article {47716, title = {The advertisement call and comments on the distribution of Eleutherodactylus bilineatus Bokermann, 1975, an endemic frog of Bahia State, Brazil (Amphibia, Anura)}, journal = {ZooKeys}, volume = {677}, year = {2017}, month = {Jun-05-2019}, pages = {151 - 159}, abstract = {

Advertisement calls can be used to aid solving taxonomic problems and understanding the evolution of certain groups. In this study, the advertisement call of Eleutherodactylus bilineatus is described. It is composed by two different notes with a total duration of 0.529\–4.241 seconds and dominant frequency of 1.72\–3.45 kHz. Additionally, new data is provided on the geographical distribution of Eleutherodactylus bilineatus and the most inland record for this species.

}, keywords = {Atlantic Forest, bioacoustics, Holoadeninae, range extension, vocalization}, issn = {1313-2989}, doi = {10.3897/zookeys.677.12309}, url = {http://zookeys.pensoft.net/articles.php?id=12309}, author = {Iuri Ribeiro Dias and Mira-Mendes, Caio Vinicius de and Souza-Costa, Carlos Augusto and Junc{\'a}, Flora Acu{\~n}a and Mirco Sol{\'e}} } @article {16169, title = {Cryptic within cryptic: genetics, morphometrics, and bioacoustics delimitate~a new species of Eleutherodactylus (Anura: Eleutherodactylidae) from Eastern Cuba}, journal = {Zootaxa}, volume = {4221}, year = {2017}, month = {Aug-01-2018}, pages = {501}, issn = {1175-5326}, doi = {10.11646/zootaxa.4221.510.11646/zootaxa.4221.5.1}, url = {http://biotaxa.org/Zootaxa/issue/view/zootaxa.4221.5}, author = {Ariel Rodr{\'\i}guez and {\'A}lvaro Dugo-Cota and Santiago Montero-Mendieta and Alejandro Gonzalez-Voyer and Roberto Alonso Bosch and Miguel Vences and Carles Vil{\`a}} } @article {16168, title = {Calls of Recently Introduced Coqu{\'\i} Frogs Do Not Interfere with Cricket Phonotaxis in Hawaii}, journal = {Journal of Insect Behavior}, year = {2017}, month = {Jul-01-2018}, issn = {0892-7553}, doi = {10.1007/s10905-017-9597-1}, url = {http://link.springer.com/10.1007/s10905-017-9597-1}, author = {Zuk, Marlene and Tanner, Jessie C. and Schmidtman, Elizabeth and Mark A. Bee and Susan L. Balenger} }