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Biomedical subjects

W S Rhode

Publications and source records attributed to W S Rhode.

8 recordsLinked to original sources
PubMed1992

Basilar membrane mechanics in the hook region of cat and guinea-pig cochleae: sharp tuning and nonlinearity in the absence of baseline position shifts.

A heterodyne laser interferometer was used to observe the movements of small (approximately 20 microns) stainless-steel beads placed on the basilar membrane in the hook region of cat and guinea-pig cochleae. In several preparations, the displacement patterns observed exhibited sharp nonlinear tuning; in one cat this tuning was comparable to that commonly observed in single auditory-nerve fibers. The most sensitive frequencies of the preparations ranged from 31-40 kHz in the cat, and 28-32 kHz in the guinea-pig. The sharp tuning and nonlinearity of the basilar membrane responses was not apparent in surgically or acoustically traumatized preparations. The response nonlinearities were susceptible to temporary threshold shifts and disappeared within a few minutes post-mortem. Stimulus-related shifts in the baseline position of the basilar membrane were not apparent at low stimulus levels. Such shifts were occasionally observed at higher stimulus levels (e.g., > 90 dB SPL), but never approached the fundamental (oscillatory) component of basilar membrane vibration in magnitude. These findings are discussed in relation to previous observations by other workers.

Acoustic Stimulation↗
PubMed1992

Basilar membrane tonotopicity in the hook region of the cat cochlea.

Middle-ear to basilar membrane (BM) velocity transfer functions are reported for seven locations in the hook region of a single cat cochlea. These transfer functions were recorded at high sound pressure levels in a linearized, or passive cochlea, and resemble those reported previously by Wilson and Evans (1983). They demonstrate longitudinal tonotopicity with a gradient of approximately 3.6 mm/octave. When allowances are made for the nonlinear mechanisms previously demonstrated in active hook region preparations (Cooper and Rhode, 1992), the data are also consistent with the tonotopic map derived from the intracellular dye-filling studies of Liberman (1982).

Acoustic Stimulation↗
PubMed1991

A composite model of the auditory periphery for the processing of speech based on the filter response functions of single auditory-nerve fibers.

A composite model of the auditory periphery, based upon a unique analysis technique for deriving filter response characteristics from cat auditory-nerve fibers, is presented. The model is distinctive in its ability to capture a significant broadening of auditory-nerve fiber frequency selectivity as a function of increasing sound-pressure level within a computationally tractable time-invariant structure. The output of the model shows the tonotopic distribution of synchrony activity of single fibers in response to the steady-state vowel [e] presented over a 40-dB range of sound-pressure levels and is compared with the population-response data of Young and Sachs (1979). The model, while limited by its time invariance, accurately captures most of the place-synchrony response patterns reported by the Johns Hopkins group. In both the physiology and in the model, auditory-nerve fibers spanning a broad tonotopic range synchronize to the first formant (F1), with the proportion of units phase-locked to F1 increasing appreciably at moderate to high sound-pressure levels. A smaller proportion of fibers maintain phase locking to the second and third formants across the same intensity range. At sound-pressure levels of 60 dB and above, the vast majority of fibers with characteristic frequencies greater than 3 kHz synchronize to F1 (512 Hz), rather than to frequencies in the most sensitive portion of their response range. On the basis of these response patterns it is suggested that neural synchrony is the dominant auditory-nerve representation of formant information under "normal" listening conditions in which speech signals occur across a wide range of intensities and against a background of unpredictable and frequently intense acoustic interference.

Animals↗
PubMed1978

Visual evoked spectrum array and interhemispheric variations.

An EEG spectrum analysis during visual stimulation was computed in 19 normal subjects. Visual stimulation consisted of trains of flashes at frequencies ranging between 2.5 and 20 flashes per second. Recordings were carried out simultaneously from the right and left occipital regions with bipolar and referential montages. Compressed spectral arrays were computed for eight-second epochs at each recording site using a fast Fourier transform. The ratio of the spectral energy from homologus regions of right and left hemispheres at each stimulation frequency was determined. The ratios were graphically displayed in a visual evoked spectrum array (VESA) ratio plot (VESA-GRAM); the mean of the ratio plot was designated the VESA coefficient. The range of variation for these measurements was determined for normal subjects. An application of the technique to patients with hemianopia showed abnormal VESA (characterized by smaller spectral amplitudes over the appropriate hemisphere), abnormal VESA ratio plots, and high VESA coefficients. These preliminary findings suggest that VESA may be a promising method to detect retrochiasmatic visual defects.

Adult↗
PubMed1978

Some observations on cochlear mechanics.

A set of experiments was conducted using the Mössbauer effect to determine the vibratory characteristics of the basilar membrane, Reissner's membrane, the malleus, incus, and oval window in squirrel monkey. A few measurements were also made in guinea pig in the basal cochlear region. The nonlinear vibration properties of the basilar membrane are described in detail for the midfrequency region in the squirrel monkey. Only in this region have nonlinear effects been observed. A comparison of mechanical and neural data indicates good qualitative agreement.

Animals↗
PubMed1978

Auditory nerve fiber response to wide-band noise and tone combinations.

1. Responses of single auditory nerve fibers to combinations of noise and tone were obtained. The results were found to depend on the relative effectiveness of each stimulus when presented alone. 2. When the response rate to one stimulus presented alone was considerably greater than the response rate to the other stimulus presented alone, the more effective stimulus dominated the responses when the two stimuli were combined. The more effective stimulus captured the response of the neuron. Thus, intense noise was found to mask responses to weaker tones, and intense tones were found to mask responses to weaker noise. This masking of the weaker stimulus is thought to enhance the signal-to-noise ratio of the most prominent response component. 3. When the two stimuli had similar effectiveness, complex interactions occurred. When the tone was near best (characteristic) frequency, partial summation effects occured. The tone partially suppressed the responses to the noise if other frequencies were used. Tones above best frequency caused particularly powerful suppression. 4. The bandwidth of the noise was varied somewhat. While bandwidth affected the effectiveness of the noise, it did not affect the types of interactions observed. 5. For a neuron which was essentially silent in the absence of acoustic stimuli, adding a weak level of noise lowered the threshold of responsiveness to the tone.

Animals↗