Perceptual organization of acoustic stimuli by budgerigars (Melopsittacus undulatus): III. Contact calls.

We trained budgerigars by operant conditioning to discriminate among a set of contact calls in a same–different task and analyzed response latencies from this task by using multidimensional-scaling (MDS) and cluster-analysis procedures. Humans listened to the same calls and indicated the similarity between pairs of calls by a direct rating procedure. An MDS program ({sindscal}) was used to arrange these complex acoustic stimuli in multidimensional space reflecting perceptual organization. Multiple regression techniques were used to identify the acoustic characteristics of contact calls that were correlated with the peceptual dimensions obtained from MDS. A number of spectral characteristics (e.g., peak frequency, rate of frequency modulation, and concentration of spectral energy) emerged as important for both budgerigars and humans, but the relative salience of these cues differed for the two species. Additional tests with two groups of budgerigars—cagemates and noncagemates—showed that experience with calls can change the salience of various acoustic characteristics used for perceptual organization and individual recognition. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Perceptual organization of acoustic stimuli by budgerigars (Melopsittacus undulatus): I. Pure tones.

A new combination of operant conditioning and psychophysical scaling procedures was used to study auditory perception in a small bird. In a same–different discrimination task, budgerigars learned to discriminate among pure tones that varied along one or more acoustic dimensions. Response latencies were used to generate a matrix of interstimulus similarities. Multidimensional scaling procedures were used to arrange these acoustic stimuli in a multidimensional space that supposedly reflects the bird's perceptual organization. For tones that varied in intensity, duration and frequency simultaneously, budgerigars were much more sensitive to frequency changes. From a set of tones that varied only in intensity, it was possible to calculate the growth of loudness with intensity for the budgerigar. For tones that varied only in frequency, budgerigars showed evidence of an "acoustic fovea" for frequency change in the spectral region of 2–4 kHz. Budgerigars and humans also differed in their perceptual grouping of tone sequences that rise, fall, or remain constant in pitch. Surprisingly, budgerigars were much less responsive to pitch contour than were humans. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Vocal development in budgerigars (Melopsittacus undulatus): Contact calls.

Budgerigars have a complex vocal repertoire, some of which develops through learning. The authors examined the course of vocal development in budgerigars from hatching to about 4 weeks postfledging (approximately 85 days old). Food-begging calls showed changes in duration, peak frequency, bandwidth, and frequency modulation with age. Within a week of fledging, each bird produced a contact call bearing a strong resemblance to a shortened version of its patterned food-begging call. By 4 weeks postfledging, budgerigar contact call repertoires often contained more than one call type, and there was clear evidence of sharing and imitation among the calls of parents, fledglings, and other social companions. Perceptual testing showed that whereas acoustic variation in the structure of developing calls decreased both within and between nestling birds, the discrimination of these calls was easier for adult birds as young birds matured. These results suggest parallels with certain aspects of language development in humans. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The discrimination of temporal fine structure in call-like harmonic sounds by birds.

Thresholds for discriminating changes in the temporal fine structure of call-like, harmonic sounds were measured in zebra finches (Taeniopygia guttata) and budgerigars (Melopsittacus undulatus). Birds could detect changes in periods as short as 1.225 ms at near 100% accuracy even when spectral and envelope cues were identical, as in time-reversed stimuli. Humans performed poorly on such stimuli, paralleling results from previous studies. Bird thresholds were in the range of those reported in neurophysiological studies of the songbird high vocal center (HVC) to temporally modified conspecific songs. Taken together, these results show that birds can hear differences in temporal fine structure in their natural vocalizations that go beyond human capabilities, but whether these abilities have communicative relevance remains to be seen. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Vocal plasticity in budgerigars (Melopsittacus undulatus): Evidence for social factors in the learning of contact calls.

Recorded distance or contact calls of 6 unrelated adult male budgerigars before and during 8 wks of social contact. The 6 birds were housed in 2 separate groups of 3 each in adjoining cages. Birds in each cage could hear but not see the birds in the neighboring cage. At the beginning of the study, none of the birds shared any contact call types. The first appearance of 1 bird's imitation of a cagemate's contact call type occurred after 1 wk. Call type repertoires continued to change; some call types dropped out of the repertoires, and others were modified over time. Birds in the same cage shared the same dominant call type 8 wks later, and the dominant call types differed between the 2 cages. Thus, budgerigars can learn calls as adults, and call type convergence is achieved through mutual vocal imitation of social companions. In the absence of social but not aural contact, vocal imitation was greatly reduced. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The surface epithelium of recurrent infected palatine tonsils is rich in gammadelta T cells

Thresholds for detecting alterations in the timbre and harmonicity of complex harmonic signals were measured in zebra finches, budgerigars, and humans. The stimuli used in this experiment were designed to have particular salience for zebra finches by modeling them after natural zebra finch calls. All 3 species showed similar abilities for detecting an amplitude decrement in a single component of a harmonic complex. However, zebra finches and budgerigars were extraordinarily sensitive to the mistunings of single harmonics and exhibited significantly lower thresholds compared with humans at 2 different fundamental frequencies, 570 Hz and 285 Hz. Randomizing relative phases of components in a harmonic stimulus resulted in a significant increase in threshold for detecting mistunings in zebra finches but not in humans. Decreasing the duration of mistuned harmonic stimuli resulted in higher thresholds for both birds and humans. The overall superiority of birds in discriminating inharmonicity suggests that birds and mammals may use different strategies in processing these complex harmonic sounds.     

Detection of changes in timbre and harmonicity in complex sounds by zebra finches (Taeniopygia guttata) and budgerigars (Melopsittacus undulatus).

Thresholds for detecting alterations in the timbre and harmonicity of complex harmonic signals were measured in zebra finches, budgerigars, and humans. The stimuli used in this experiment were designed to have particular salience for zebra finches by modeling them after natural zebra finch calls. All 3 species showed similar abilities for detecting an amplitude decrement in a single component of a harmonic complex. However, zebra finches and budgerigars were extraordinarily sensitive to the mistunings of single harmonics and exhibited significantly lower thresholds compared with humans at 2 different fundamental frequencies, 570 Hz and 285 Hz. Randomizing relative phases of components in a harmonic stimulus resulted in a significant increase in threshold for detecting in zebra finches but not in humans. Decreasing the duration of mistuned harmonic stimuli resulted in higher thresholds for both birds and humans. The overall superiority of birds in discriminating inharmonicity suggests that birds and mammals may use different strategies in processing these complex harmonic sounds. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Auditory perception of conspecific and heterospecific vocalizations in birds: Evidence for special processes.

Budgerigars (Melopsittacus undulatus), canaries (Serinus canaria), and zebra finches (Poephila guttata castanotis) were tested for their ability to discriminate among distance calls of each species. For comparison, starlings (Sturnus vulgaris) were tested on the same sounds. Response latencies to detect a change in a repeating background of sound were taken as a measure of the perceptual similarity among calls. All 4 species showed clear evidence of 3 perceptual categories corresponding to the calls of the 3 species. Also, budgerigars, canaries, and zebra finches showed an enhanced ability to discriminate among calls of their own species over the calls of others. Starlings discriminated more efficiently among canary calls than among budgerigar or zebra finch calls. Results show species differences in discrimination of species-specific acoustic communication signals and provide insight into the nature of specialized perceptual processes. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effect of acoustic cue modifications on evoked vocal response to calls in zebra finches (Taeniopygia guttata).

Besides their song, which is usually a functionally well-defined communication signal with an elaborate acoustic structure, songbirds also produce a variety of shorter vocalizations named calls. While a considerable amount of work has focused on information coding in songs, little is known about how calls' acoustic structure supports communication processes. Because male and female zebra finches use calls during most of their interactions and answer to conspecific calls without visual contact, we aimed at identifying which calls' acoustic cues are necessary to elicit a vocal response. Using synthetic zebra finch calls, we examined evoked vocal response of male and female zebra finches to modified versions of the distance calls. Our results show that the vocal response of zebra finches to female calls requires the full harmonic structure of the call, whereas the frequency downsweep of male calls is necessary to evoke a vocal response. It is likely that both female and male calls require matching a similar frequency bandwidth to trigger a response in conspecific individuals. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Control of vocal repertoire by reward in budgerigars (Melopsittacus undulatus).

The calls of some bird species may be modified by reward and punishment. However, the operant control of vocal topographies (i.e., the effect of reward or punishment on the physical dimensions of a vocal response) in such species has not been extensively explored. Using a computer-based, real-time system for rewarding vocalizations with food, the authors placed 3 budgerigars under a frequency-dependent reward schedule. During a session, the budgerigars received food for each vocalization that differed from the last N rewarded vocalizations. It was found that each of the budgerigars adapted their vocalizations to this procedure. When the value of N was 1 or 2, the birds "solved" the frequency-dependent schedule by developing N ?+?1 call types and used a simple "win stay, lose switch" sequencing strategy. At N?=?3, 1 of the birds again produced N ?+?1 (i.e., 4) call types, and another solved the criterion by markedly increasing call variability. New calls developed from the elements of old call types and using multidimensional scaling techniques, the authors traced the evolution of each new call type from the previous experimental call repertoire. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Toward articulatory-acoustic models for liquid approximants based on MRI and EPG data. Part II. The rhotics

Magnetic resonance images of the vocal tract during sustained production of [symbol: see text] by four native American English talkers are employed for measuring vocal-tract dimensions and for morphological analysis of the 3D vocal tract and tongue shapes. Electropalatography contact profiles are used for studying inter- and intra-talker variabilities. The vocal tract during the production of [symbol: see text] appears to be characterized by three cavities due to the presence of two supraglottal constrictions: the primary one in the oral cavity, and a secondary one in the pharyngeal cavity. All subjects show a large volume anterior to the oral constriction, which results from an inward-drawn tongue body, an anterior tongue body that is characterized by convex cross sections, and a concave posterior tongue body shape. Inter-subject variabilities are observed in the oral-constriction location and the way the constriction is formed. No systematic differences are found between the 3-D vocal tract and tongue shapes of word-initial and syllabic [symbol: see text]s. Tongue-shaping mechanisms for these sounds and their acoustic implications are discussed.     

Effects of deafening on the development of nestling and juvenile vocalizations in budgerigars (Melopsittacus undulatus).

The effects of complete and partial cochlear extirpation at ages 9–11 days posthatch were assessed in 5 nestling budgerigars (Melopsittacus undulatus) to determine if auditory feedback is necessary for the production of nestling vocalizations. Although early deafening had no effect on the production of food-begging calls produced during the first 2 weeks posthatch, deafening did disrupt the expected transition from these early calls to the longer and more complex frequency-modulated, patterned food-begging calls normally appearing 3–4 weeks posthatch. All birds sustaining either complete or partial cochlear extirpation failed to develop stereotyped contact calls around the time of fledging at 5 weeks. These results are consistent with previous research showing that deafened nestlings do not develop normal contact calls (R. J. Dooling, B. R Gephart, P. H. Price, C. McHale, & S. E. Brauth; see record 1989-32132-001) and also indicate that a form of sensorimotor learning is involved in the production of mature, patterned food-begging calls in budgerigars. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Hearing and vocalizations of wild-caught Australian budgerigars (Melopsittacus undulatus).

This study examined the hearing and contact calls of wild-caught Australian budgerigars (Melopsittacus undulatus) and compared these data to hearing and vocalizations in the much more extensively studied domesticated budgerigar. The spectral energy in the contact calls of both wild-caught and domesticated budgerigars falls almost exclusively in the frequency of 2–4 kHz. Absolute and masked thresholds were similar in both groups of birds. Similar to the results found in domesticated birds, critical ratio functions for the wild-caught budgerigars decreased at frequencies of 1.0 kHz–2.86 kHz and then increased again dramatically at frequencies above 2.86 kHz. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Perception of species-specific contact calls by budgerigars (Melopsittacus undulatus).

In Exp I, 3 budgerigars were trained with operant techniques to discriminate examples of species-specific contact calls (5 male and 5 female). In Exp II, Ss were tested on vocalizations from 5 male and 5 female canaries. Ss showed an equivalent ability to discriminate and remember both budgerigar and canary calls. Additional tests (Exps III and IV) showed that both temporal and spectral cues were important in Ss' discrimination of species-specific calls. However, spectral cues occurring in the region of 2.0–4.0 kHz appeared to be critical for the discrimination. Results support the notion of a generalized, but highly sophisticated, perceptual learning system in the budgerigar for the processing of vocal signals. The perceptual and memory skills involved in this learning system are discussed. (38 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Whistle rates of wild bottlenose dolphins (Tursiops truncatus): Influences of group size and behavior.

In large social groups acoustic communication signals are prone to signal masking by conspecific sounds. Bottlenose dolphins (Tursiops truncatus) use highly distinctive signature whistles that counter masking effects. However, they can be found in very large groups where masking by conspecific sounds may become unavoidable. In this study we used passive acoustic localization to investigate how whistle rates of wild bottlenose dolphins change in relation to group size and behavioral context. We found that individual whistle rates decreased when group sizes got larger. Dolphins displayed higher whistle rates in contexts when group members were more dispersed as in socializing and in nonpolarized movement than during coordinated surface travel. Using acoustic localization showed that many whistles were produced by groups nearby and not by our focal group. Thus, previous studies based on single hydrophone recordings may have been overestimating whistle rates. Our results show that although bottlenose dolphins whistle more in social situations they also decrease vocal output in large groups where the potential for signal masking by other dolphin whistles increases. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Convergence of calls as animals form social bonds, active compensation for noisy communication channels, and the evolution of vocal learning in mammals.

The classic evidence for vocal production learning involves imitation of novel, often anthropogenic sounds. Among mammals, this has been reported for dolphins, elephants, harbor seals, and humans. A broader taxonomic distribution has been reported for vocal convergence, where the acoustic properties of calls from different individuals converge when they are housed together in captivity or form social bonds in the wild. Vocal convergence has been demonstrated for animals as diverse as songbirds, parakeets, hummingbirds, bats, elephants, cetaceans, and primates. For most species, call convergence is thought to reflect a group-distinctive identifier, with shared calls reflecting and strengthening social bonds. A ubiquitous function for vocal production learning that is starting to receive attention involves modifying signals to improve communication in a noisy channel. Pooling data on vocal imitation, vocal convergence, and compensation for noise suggests a wider taxonomic distribution of vocal production learning among mammals than has been generally appreciated. The wide taxonomic distribution of this evidence for vocal production learning suggests that perhaps more of the neural underpinnings for vocal production learning are in place in mammals than is usually recognized. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Salience of Caller Identity in Rhesus Monkey (Macaca mulatta) Coos and Screams: Perceptual Experiments With Human (Homo sapiens) Listeners.

Recent evidence from acoustic analysis and playback experiments indicates that adult female rhesus monkey (Macaca mulatta) coos are individually distinctive but their screams are not. In this study, the authors compared discrimination of individual identity in these sounds by naive human listeners who judged whether 2 sounds had been produced by the same monkey or 2 monkeys. Each of 3 experiments using this same-different design showed significantly better discrimination of vocalizer identity from coos than from screams. Experiment 1 demonstrated the basic finding. Experiment 2 also tested the effect of non-identity-related scream variation, and Experiment 3 added a comparison with human vowel sounds. Outcomes suggest that acoustic structural differences in coos and screams influence salience of caller-identity cues, with significant implications for understanding the functions of these calls. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Perception of mistuned harmonics in complex sounds by the bullfrog (Rana catesbeiana).

The ability of 73 male bullfrogs (Rana catesbeiana) to detect single mistuned harmonics in an otherwise periodic signal was studied. Bullfrogs in their natural environment were presented with playbacks of synthetic signals, resembling their species advertisement calls, that differed in the frequency of 1 harmonic component (out of 22). There were significant differences in the number and latency of the males' evoked vocal responses to these stimuli, suggesting that males were sensitive to the differences between the sounds. Differences in envelope shape (rate and depth of amplitude modulation) produced by the harmonic mistunings may underlie the differences in response. Frogs, like birds and humans, can discriminate sounds on the basis of harmonic structure, indicating that this is a general perceptual trait shared among vertebrates. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Cortical Responses in Rats Predict Perceptual Sensitivities to Complex Sounds.

The common assumption that perceptual sensitivities are related to neural representations of sensory stimuli has seldom been directly demonstrated. The authors analyzed the similarity of spike trains evoked by complex sounds in the rat auditory cortex and related cortical responses to performance in an auditory task. Rats initially learned to identify 2 highly different periodic, frequency-modulated sounds and then were tested with increasingly similar sounds. Rats correctly classified most novel sounds; their accuracy was negatively correlated with acoustic similarity. Rats discriminated novel sounds with slower modulation more accurately than sounds with faster modulation. This asymmetry was consistent with similarities in cortical representations of the sounds, demonstrating that perceptual sensitivities to complex sounds can be predicted from the cortical responses they evoke. (PsycINFO Database Record (c) 2010 APA, all rights reserved)