Trade-off in short- and long-distance communication in tungara (Physalaemus pustulosus) and cricket (Acris crepitans) frogs

Female phonotaxis in túngara(Physalaemus pustulosus)and cricket (Acris crepitans) frogsis biased toward male advertisementcalls or call components of lowerfrequency. This behavioralbias might result in part from a mismatch betweenthe spectralcharacteristics of the advertisement call and the most sensitivefrequencyof the peripheral end organ implicated in reception of thesesounds.In both species, females are tuned to frequencies lowerthan average for thecalls in their population. This mismatch,however, represents the situationduring short-distance communication.Female frogs can also use the call todetect choruses at longdistances, and the spectral distribution of callenergy canvary with transmission distance. We used computer simulationstotest the hypothesis that there is a better match betweentuning and callspectral energy at long distances from the callingmale than at shortdistances by comparing the performance (soundenergy received) of the naturaltuning curve relative to anoptimal tuning curve (i.e., one centered at thecall's dominantfrequency). The relative performance of the natural tuningcurveincreased with distance in túngarafrogs. For the twosubspecies of cricket frogs, however, the relativeperformancedecreased at longer distances. The performance did not equaltheoptimal tuning curve at the distances tested. The resultsindicate that therelationship between calls and auditory tuningcannot be optimal for both longand short distance reception.The relationship between female tuning and calldominant frequencymay represent a compromise between short and long distancecommunication,and the bias toward short or long distances may vary amongspecies.     

BLUE WHALE, BALAENOPTERA MUSCULUS, VOCALIZATIONS FROM THE WATERS OFF CENTRAL CALIFORNIA

Low-frequency calls produced by blue whales, Balaenoptera musculus , were recorded in the northeastern Pacific Ocean off central California. Two blue whales were sighted during a vessel-based marine mammal survey, and when sonobuoys were subsequently deployed, blue whale calls were recorded. A third recording was obtained during the survey from a blue whale that was not seen. Recordings with 15, 25, and 55 min of calls were obtained from these individuals. The three recordings all contain two-part, low-frequency calls with slight interindividual variation. The calls consist of an amplitude modulated (AM) signal with a mean center frequency of 16.5 Hz, followed by a downsweep whose mean center frequency sweeps from 18.2 Hz to 16.6 Hz. The recordings are compared with blue whale recordings from the Pacific and Atlantic Oceans. The geographic variability suggests that blue whale calls may be used as an acoustic indicator of stock identity.     

Fluctuating asymmetries and advertisement call variation in the cricket frog, Acris crepitans

We used an anuran acoustic communication system to test a predictionof the "fluctuating asymmetries/good genes" hypothesis thatfemales prefer more symmetric mates because symmetry indicatesgenetic quality. Mate preferences of female cricket frogs (Acriscrepitans) can be influenced by three call characters: dominantfrequency, numbers of pulses per call, and number of pulse groupsper call. We tested the hypothesis that these preferences resultin females preferring more symmetric males. We measured fluctuatingasymmetries of characters not involved with the communicationsystem (head and tibia), and those involved in signal production(laryngeal characters) and signal reception (aural characters).We determined whether the asymmetries in these characters wererelated to the three variables that enhance call attractiveness.Most of the multiple regression models showed no significantassociation between the fluctuating asymmetries of charactersand any of the calls. The regression of head and tibia fluctuatingasymmetry on pulse number was significant, but partial regressioncoefficients revealed that more pulses were associated witha more symmetric head length and a less symmetric tibia length.Our findings provide little or no support for the fluctuatingasymmetries/good genes hypothesis. We emphasize, however, thatthis hypothesis should not be abandoned based on negative resultsof a single study, but deserves further scrutiny.     

Syntactic structure and geographical dialects in the songs of male rock hyraxes

Few mammalian species produce vocalizations that are as richly structured as bird songs, and this greatly restricts the capacity for information transfer. Syntactically complex mammalian vocalizations have been previously studied only in primates, cetaceans and bats. We provide evidence of complex syntactic vocalizations in a small social mammal: the rock hyrax (Procavia capensis: Hyracoidea). We adopted three algorithms, commonly used in genetic sequence analysis and information theory, to examine the order of syllables in hyrax calls. Syntactic dialects exist, and the syntax of hyrax calls is significantly different between different regions in Israel. Call syntax difference is positively correlated to geographical distance over short distances. No correlation is found over long distances, which may reflect limited dispersal movement. These findings indicate that rich syntactic structure is more common in the vocalizations of mammalian taxa than previously thought and suggest the possibility of vocal production learning in the hyrax.     

STRUCTURE AND FUNCTION IN WHALE EARS

ABSTRACT

Ultrasonic echolocation abilities are well documented in several dolphin species, but hearing characteristics are unknown for most whales. Vocalization data suggest whale hearing spans infra- to ultrasonic ranges. This paper presents an overview of whale ear anatomy and analyzes 1) how whale ears are adapted for underwater hearing and 2) how inner ear differences relate to different hearing capacities among whales.

Whales have adaptations for rapid, deep diving and long submersion; e.g., broad- bore Eustachian tubes, no pinnae, and no air-filled external canals, that impact sound reception. In odontocetes, two soft tissue channels conduct sound to the ear. In mysticetes, bone and soft tissue conduction are likely. The middle ear is air-filled but has an extensible mucosa. Cochlear structures are hypertrophied and vestibular components are reduced. Auditory ganglion cell densities are double land mammal averages (2000–4000/mm). Basilar membrane lengths range 20–70 mm; gradients are larger than in terrestrial mammals. Odontocetes have 20–60% bony membrane support and basal ratios >0.6, consistent with hearing >150 kHz. Mysticetes have apical ratios <0.002 and no bony lateral support, implying acute infrasonic hearing. Cochlear hypertrophy may be adaptive for high background noise. Vestibular loss is consistent with cervical fusion. Exceptionally high auditory fiber counts suggest both mysticetes and odontocetes have ears “wired” for more complex signal processing mechanisms than most land mammals.     

SOUND PRODUCTION AND SOUND EMISSION IN SEVEN SPECIES OF EUROPEAN TETTIGONIIDS PART III. DETERMINATION OF THE MECHANISM OF SOUND PRODUCTION USING CEPSTRUM ANALYSIS

ABSTRACT

The mechanism of sound production in tettigoniids is examined by applying the method of ‘cepstrum’ analysis to insect calls. The power cepstrum is defined as the inverse Fourier transform of the logarithmic power spectrum. This analysis shows that the tettigoniid sound signal is a convolution in time of probably two components. The first is caused by the initial impact of teeth of the stridulatory file on the left wing against the plectrum on the right wing (termed the input pulse); the second is caused by the oscillating properties of the tegmina (these being a function of the intrinsic frequencies of dorsal fields and mirror and their damping properties). In the cepstrum each component appears as a varying number of peaks. The tooth impacts cause a very low quefrency peak probably representing the time in which the two tegmina are in contact during each impact and high quefrency peaks representing the impulse repetition rate. The oscillating properties of the tegmina cause two major quefrency peaks which can be clearly related to the size of the dorsal fields and of the mirror respectively, and therefore to their intrinsic frequencies. The high damping factor of the tegmina together with the transient shape of the tegminal input pulse causes a strong time limitation of the impulses and is therefore responsible for the broad frequency bands occurring in the power spectra of the tettigoniid songs. The impulse generation of a synthetic tettigoniid song is discussed.