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Fluid volume displacement at the oval and round windows with air and bone conduction stimulation.

The fluids in the cochlea are normally considered incompressible, and the fluid volume displacement of the oval window (OW) and the round window (RW) should be equal and of opposite phase. However, other channels, such as the cochlear and vestibular aqueducts, may affect the fluid flow. To test if the OW and RW fluid flows are equal and of opposite phase, the volume displacement was assessed by multiple point measurement at the windows with a laser Doppler vibrometer. This was done during air conduction (AC) stimulation in seven fresh human temporal bones, and with bone conduction (BC) stimulation in eight temporal bones and one human cadaver head. With AC stimulation, the average volume displacement of the two windows is within 3 dB, and the phase difference is close to 180 degrees for the frequency range 0.1 to 10 kHz. With BC stimulation, the average volume displacement difference between the two windows is greater: below 2 kHz, the volume displacement at the RW is 5 to 15 dB greater than at the OW and above 2 kHz more fluid is displaced at the OW. With BC stimulation, lesions at the OW caused only minor changes of the fluid flow at the RW.

Acoustic Stimulation↗

Inferred basilar-membrane response functions for listeners with mild to moderate sensorineural hearing loss.

Psychophysical estimates of cochlear function suggest that normal-hearing listeners exhibit a compressive basilar-membrane (BM) response. Listeners with moderate to severe sensorineural hearing loss may exhibit a linearized BM response along with reduced gain, suggesting the loss of an active cochlear mechanism. This study investigated how the BM response changes with increasing hearing loss by comparing psychophysical measures of BM compression and gain for normal-hearing listeners with those for listeners who have mild to moderate sensorineural hearing loss. Data were collected from 16 normal-hearing listeners and 12 ears from 9 hearing-impaired listeners. The forward masker level required to mask a fixed low-level, 4000-Hz signal was measured as a function of the masker-signal interval using a masker frequency of either 2200 or 4000 Hz. These plots are known as temporal masking curves (TMCs). BM response functions derived from the TMCs showed a systematic reduction in gain with degree of hearing loss. Contrary to current thinking, however, no clear relationship was found between maximum compression and absolute threshold.

Adult↗

The influence of duration and level on human sound localization.

The localization of sounds in the vertical plane (elevation) deteriorates for short-duration wideband sounds at moderate to high intensities. The effect is described by a systematic decrease of the elevation gain (slope of stimulus-response relation) at short sound durations. Two hypotheses have been proposed to explain this finding. Either the sound localization system integrates over a time window that is too short to accurately extract the spectral localization cues (neural integration hypothesis), or the effect results from cochlear saturation at high intensities (adaptation hypothesis). While the neural integration model predicts that elevation gain is independent of sound level, the adaptation hypothesis holds that low elevation gains for short-duration sounds are only obtained at high intensities. Here, these predictions are tested over a larger range of stimulus parameters than has been done so far. Subjects responded with rapid head movements to noise bursts in the two-dimensional frontal space. Stimulus durations ranged from 3 to 100 ms; sound levels from 26 to 73 dB SPL. Results show that the elevation gain decreases for short noise bursts at all sound levels, a finding that supports the integration model. On the other hand, the short-duration gain also decreases at high sound levels, which is in line with the adaptation hypothesis. The finding that elevation gain was a nonmonotonic function of sound level for all sound durations, however, is predicted by neither model. It is concluded that both mechanisms underlie the elevation gain effect and a conceptual model is proposed to reconcile these findings.

Adult↗

Temporal effects in simultaneous masking with on- and off-frequency noise maskers: effects of signal frequency and masker level.

Temporal effects in simultaneous masking were measured as a function of masker level for an on-frequency broadband masker and an off-frequency narrow-band masker for signal frequencies of 750, 1730, and 4000 Hz. The on-frequency masker was 10 equivalent rectangular bandwidths (ERBs) wide and centered at the signal frequency; the off-frequency masker was 500 Hz wide and its lower frequency edge was 1.038 ERBs higher in frequency than the signal. The primary goal of the study was to determine whether previously observed differences regarding the effects of signal frequency and masker level on the temporal effect for these two different types of masker might be due to considerably different signal levels at threshold. Despite similar masked thresholds, the effects of signal frequency and masker level in the present study were different for the two masker types. The temporal effect was significant for the two highest frequencies and absent for the lowest frequency in the presence of the broadband masker, but was more or less independent of frequency for the narrow-band masker. The temporal effect increased but then decreased as a function of level for the broadband masker (at the two higher signal frequencies, where there was a temporal effect), but increased and reached an asymptote for the narrow-band masker. Despite the different effects of signal frequency and masker level, the temporal effects for both types of masker can be understood in terms of a basilar-membrane input-output function that becomes more linear during the course of masker stimulation.

Acoustic Stimulation↗

Siamang gibbons exceed the saccular threshold: intensity of the song of Hylobates syndactylus.

Measurements are reported of the intensity of the siamang gibbon loud call obtained from the vocal bouts of three family groups at Twycross Zoo, UK. Across 25 samples the maximum intensity ranged from 95 to 113 dB SPL (linear frequency-weighting and fast time-weighting) and exhibited three frequency modes of 250-315 Hz, 630-800 Hz and 1.2-1.6 kHz. The lowest frequency mode, which may correspond to the "boom" sound produced by resonance of the siamang inflated vocal sac, had a mean maximum intensity of 99 dB SPL. These values, which are in excess of the saccular acoustic threshold of about 90 dB at 300 Hz for air conducted sound, suggest that primate loud calls recruit a primitive mode of acoustic sensitivity furnished by the sacculus. Thus reproductive vocal behavior of primates may be influenced by a primitive acoustical reward pathway inherited from a common ancestor with anamniotes. In humans such a pathway could explain the compulsion for exposure to loud music.

Animals↗

Similarity in loudness and distortion product otoacoustic emission input/output functions: implications for an objective hearing aid adjustment.

The aim of the present study was to compare distortion product otoacoustic emissions (DPOAEs) to loudness with regard to the potentiality of DPOAEs to determine characteristic quantities of the cochlear-impaired ear and to derive objective hearing aid parameters. Recently, Neely et al. [J. Acoust. Soc. Am. 114, 1499-1507 (2003)] compared DPOAE input/output functions to the Fletcher and Munson [J. Acoust. Soc. Am. 5, 82-108 (1933)] loudness function finding a close resemblance in the slope characteristics of both measures. The present study extended their work by performing both loudness and DPOAE measurements in the same subject sample, and by developing a method for the estimation of gain needed to compensate for loss of cochlear sensitivity and compression. DPOAEs and loudness exhibited similar behavior when plotted on a logarithmic scale and slope increased with increasing hearing loss, confirming the findings of Neely et al. To compensate for undesired nonpathological impacts on the magnitude of DPOAE level, normalization of DPOAE data was implemented. A close resemblance between gain functions based on loudness and normalized DPOAE data was achieved. These findings suggest that DPOAEs are able to quantify the loss of cochlear sensitivity and compression and thus might provide parameters for a noncooperative hearing aid adjustment.

Acoustic Stimulation↗

Testing the concept of softness imperception: loudness near threshold for hearing-impaired ears.

Buus and Florentine [J. Assoc. Res. Otolaryngol. 3, 120-139 (2002)] have proposed that loudness recruitment in cases of cochlear hearing loss is caused partly by an abnormally large loudness at absolute threshold. This has been called "softness imperception." To evaluate this idea, loudness-matching functions were obtained using tones at very low sensation levels. For subjects with asymmetrical hearing loss, matches were obtained for a single frequency across ears. For subjects with sloping hearing loss, matches were obtained between tones at two frequencies, one where the absolute threshold was nearly normal and one where there was a moderate hearing loss. Loudness matching was possible for sensation levels (SLs) as low as 2 dB. When the fixed tone was presented at a very low SL in an ear (or at a frequency) where there was hearing impairment, it was matched by a tone with approximately the same SL in an ear (or at a frequency) where hearing was normal (e.g., 2 dB SL matched 2 dB SL). This relationship held for SLs up to 4-10 dB, depending on the subject. These results are not consistent with the concept of softness imperception.

Adult↗

Equal-loudness-level contours for pure tones.

Equal-loudness-level contours provide the foundation for theoretical and practical analyses of intensity-frequency characteristics of auditory systems. Since 1956 equal-loudness-level contours based on the free-field measurements of Robinson and Dadson [Br. J. Appl. Phys. 7, 166-181 (1956)] have been widely accepted. However, in 1987 some questions about the general applicability of these contours were published [H. Fastl and E. Zwicker, Fortschritte der Akustik, DAGA '87, pp. 189-193 (1987)]. As a result, a new international effort to measure equal-loudness-level contours was undertaken. The present paper brings together the results of 12 studies starting in the mid-1980s to arrive at a new set of contours. The new contours estimated in this study are compared with four sets of classic contours taken from the available literature. The contours described by Fletcher and Munson [J. Acoust. Soc. Am. 5, 82-108 (1933)] exhibit some overall similarity to our proposed estimated contours in the mid-frequency range up to 60 phons. The contours described by Robinson and Dadson exhibit clear differences from the new contours. These differences are most pronounced below 500 Hz and the discrepancy is often as large as 14 dB.

Auditory Threshold↗

Monaural and interaural intensity discrimination: level effects and the "binaural advantage".

This study examined whether the level effects seen in monaural intensity discrimination (Weber's law and the "near miss") in a two-interval task are also observed in discrimination of interaural intensity differences (IIDs) in a single-interval task. Both tasks were performed for various standard levels of 4-kHz pure tones and broadband noise. The Weber functions (10 log deltaI/I versus I in dB) in the monaural and binaural conditions were parallel. For noise, the Weber functions had slopes close to zero (Weber's law) while the Weber functions for the tones had a mean slope of -0.089 (near miss). The near miss for the monaural and binaural tasks with tones was eliminated when a high-pass masker was gated with the listening intervals. The near-miss was also observed for 250- and 1000-Hz tones in the binaural task despite overall decreased sensitivity to changes in IID at 1000 Hz. The binaural thresholds showed a small (about 2-dB) advantage over monaural thresholds only in the broadband noise conditions. More important, however, is the fact that the level effects seen monaurally are also seen binaurally. This suggests that the basic mechanisms responsible for Weber's law and the near miss are common to monaural and binaural processing.

Acoustic Stimulation↗

Amplification and spectral shifts of vocalizations inside burrows of the frog Eupsophus calcaratus (Leptodactylidae).

A variety of animals that communicate by sound emit signals from sites favoring their propagation, thereby increasing the range over which these sounds convey information. A different significance of calling sites has been reported for burrowing frogs Eupsophus emiliopugini from southern Chile: the cavities from which these frogs vocalize amplify conspecific vocalizations generated externally, thus providing a means to enhance the reception of neighbor's vocalizations in chorusing aggregations. In the current study the amplification of vocalizations of a related species, E. calcaratus, is investigated, to explore the extent of sound enhancement reported previously. Advertisement calls broadcast through a loudspeaker placed in the vicinity of a burrow, monitored with small microphones, are amplified by up to 18 dB inside cavities relative to outside. The fundamental resonant frequency of burrows, measured with broadcast noise and pure tones, ranges from 842 to 1836 Hz and is significantly correlated with the burrow's length. Burrows change the spectral envelope of incoming calls by increasing the amplitude of lower relative to higher harmonics. The call amplification effect inside burrows of E. calcaratus parallels the effect reported previously for E. emiliopugini, and indicates that the acoustic properties of calling sites may affect signal reception by burrowing animals.

Acoustics↗

Spectral loudness summation and simple reaction time.

The present study evaluates the relation between loudness and simple reaction time (RT). Loudness matches between a narrowband noise (125 Hz wide) and a broadband noise (1500 Hz) were made at levels from near threshold to near 100 dB SPL. Over a similarly wide range of levels, RT to each of the noise bands was also measured. As reported often in previous loudness-matching studies, loudness summation depended strongly on level. With increasing SPL, the level difference between the noises needed to keep them equally loud first increased, to around 10 dB at moderate levels, and then decreased. Except for one listener, the RT data show the same pattern. The level difference needed to keep RT to the two noises the same first increased and then decreased. These results show that RT is closely related to loudness, but not to sensation level. If RT depended on sensation level, the level difference between the two noises needed to achieve equal RT would not change with SPL because the difference in sensation level between two sounds is a constant. Overall, the average results provide strong support for the contention that simple RT and loudness are closely related.

Adult↗

Subjective response of people to simulated sonic booms in their homes.

In order to determine the effect of the number of sonic boom occurrences on annoyance, a computer-based system was developed for studying the subjective response of people to the occurrence of simulated sonic booms in their homes. The system provided a degree of control over the noise exposure not found in community surveys and a degree of situational realism not available in the laboratory. A system was deployed for eight weeks in each of 33 homes. Each day from 4 to 63 sonic booms were played as the test subject went about his or her normal activities. At the end of the day, the test subjects rated their annoyance to the sonic booms heard during the day. The sonic booms consisted of different combinations of waveforms, levels, and occurrence rates. The experiment confirmed that the increase in annoyance resulting from multiple occurrences can be modeled by the addition of the term "10 * log(number of occurrences)" to the sonic boom level. Of several noise metrics considered, perceived level was the best annoyance predictor. Comparisons of the subjective responses to the different sonic boom waveforms found no differences that were not accounted for by the noise metrics.

Adaptation, Physiological↗

Effects of pulse rate and electrode array design on intensity discrimination in cochlear implant users.

The effects of pulse rate on intensity discrimination were evaluated in 14 subjects with Clarion C-I cochlear implants. Subjects had a standard [Clarion spiral electrode array (SPRL group)] or perimodiolar electrode array [Clarion HiFocus electrode array with electrode positioning system (HF+EPS group)]. Weber fractions for intensity discrimination [ Wf(dB)= 10 log deltaI/I] were evaluated at five levels over dynamic range at each of three pulse rates (200, 1625 and 6500 pps) using monopolar stimulation. Weber fractions were smaller for 200 pps stimuli than for 1625 or 6500 pps stimuli in both groups. Weber fractions were significantly smaller for SPRL subjects (mean Wf(dB) = -9.1 dB) than for HF+EPS subjects (mean Wf(dB) = -6.7 dB). Intensity difference limens (DLs) expressed as a percentage of dynamic range (DR) (deltaI%DR= deltaI/DRdB* 100) did not vary systematically with pulse rate in either group. Larger intensity DLs combined with smaller dynamic ranges led to fewer intensity steps over the dynamic range for HF+EPS subjects (average 9 steps) compared to SPRL subjects (average 23 steps). The observed effects of pulse rate and electrode array design may stem primarily from an inverse relationship between absolute current amplitude and the size of intensity DLs. The combination of smaller dynamic ranges and larger Weber fractions in HF+EPS subjects could be the result of increased variability of neural outputs in these subjects.

Adult↗

The role of noise sensitivity in the noise-response relation: a comparison of three international airport studies.

In order to examine the role of noise sensitivity in response to environmental noise, this paper presents detailed comparisons of socio-acoustic studies conducted around international airports in Amsterdam, Sydney, and London. Earlier findings that noise sensitivity moderates the effect of noise on annoyance were examined to see if they could be replicated in each of the datasets, independent of the technique of measuring noise sensitivity. The relation between exposure to aircraft noise and noise annoyance was studied separately for groups of individuals with low, medium, and high noise sensitivity, with statistical adjustment for relevant confounders. Results support the previous findings that noise sensitivity is an independent predictor of annoyance and adds to the prediction of noise annoyance afforded by noise exposure level by up to 26% of explained variance. There is no evidence of a moderating effect, whereby the covariation between noise exposure level and annoyance is weak for people who score at the extreme high or low end of the sensitivity scale, and strong for people who score in the middle of the sensitivity scale. Generally, noise sensitivity appears to increase annoyance independently of the level of noise exposure after adjustment for relevant confounders. These findings were consistent across the three datasets.

Adolescent↗

Measures for assessing architectural speech security (privacy) of closed offices and meeting rooms.

Objective measures were investigated as predictors of the speech security of closed offices and rooms. A new signal-to-noise type measure is shown to be a superior indicator for security than existing measures such as the Articulation Index, the Speech Intelligibility Index, the ratio of the loudness of speech to that of noise, and the A-weighted level difference of speech and noise. This new measure is a weighted sum of clipped one-third-octave-band signal-to-noise ratios; various weightings and clipping levels are explored. Listening tests had 19 subjects rate the audibility and intelligibility of 500 English sentences, filtered to simulate transmission through various wall constructions, and presented along with background noise. The results of the tests indicate that the new measure is highly correlated with sentence intelligibility scores and also with three security thresholds: the threshold of intelligibility (below which speech is unintelligible), the threshold of cadence (below which the cadence of speech is inaudible), and the threshold of audibility (below which speech is inaudible). The ratio of the loudness of speech to that of noise, and simple A-weighted level differences are both shown to be well correlated with these latter two thresholds (cadence and audibility), but not well correlated with intelligibility.

Architecture↗

The temporal representation of speech in a nonlinear model of the guinea pig cochlea.

The temporal representation of speechlike stimuli in the auditory-nerve output of a guinea pig cochlea model is described. The model consists of a bank of dual resonance nonlinear filters that simulate the vibratory response of the basilar membrane followed by a model of the inner hair cell/auditory nerve complex. The model is evaluated by comparing its output with published physiological auditory nerve data in response to single and double vowels. The evaluation includes analyses of individual fibers, as well as ensemble responses over a wide range of best frequencies. In all cases the model response closely follows the patterns in the physiological data, particularly the tendency for the temporal firing pattern of each fiber to represent the frequency of a nearby formant of the speech sound. In the model this behavior is largely a consequence of filter shapes; nonlinear filtering has only a small contribution at low frequencies. The guinea pig cochlear model produces a useful simulation of the measured physiological response to simple speech sounds and is therefore suitable for use in more advanced applications including attempts to generalize these principles to the response of human auditory system, both normal and impaired.

Animals↗

Rapid adaptation to foreign-accented English.

This study explored the perceptual benefits of brief exposure to non-native speech. Native English listeners were exposed to English sentences produced by non-native speakers. Perceptual processing speed was tracked by measuring reaction times to visual probe words following each sentence. Three experiments using Spanish- and Chinese-accented speech indicate that processing speed is initially slower for accented speech than for native speech but that this deficit diminishes within one minute of exposure. Control conditions rule out explanations for the adaptation effect based on practice with the task and general strategies for dealing with difficult speech. Further results suggest that adaptation can occur within as few as two to four sentence-length utterances. The findings emphasize the flexibility of human speech processing and require models of spoken word recognition that can rapidly accommodate significant acoustic-phonetic deviations from native language speech patterns.

Adaptation, Psychological↗