Basilar-membrane nonlinearity and the growth of forward masking

1998 ◽  
Vol 103 (3) ◽  
pp. 1598-1608 ◽  
Author(s):  
Christopher J. Plack ◽  
Andrew J. Oxenham
PLoS ONE ◽  
2017 ◽  
Vol 12 (3) ◽  
pp. e0174776 ◽  
Author(s):  
Michal Fereczkowski ◽  
Morten L. Jepsen ◽  
Torsten Dau ◽  
Ewen N. MacDonald

2020 ◽  
Author(s):  
Gerard Encina-Llamas ◽  
Jens Thuren Lindahl ◽  
Bastian Epp

AbstractMethods based on psychoacoustical forward masking have been proposed to estimate the local compressive growth of the basilar membrane (BM). This results from normal outer hair cells function, which leads to level-dependent amplification of BM vibration. Psychoacoustical methods assume that cochlear processing can be isolated from the response of the overall system, that sensitivity is dominated by the tonotopic location of the probe and that the effect of forward masking is different for on- and off-characteristic frequency (CF) maskers. In the present study, a computational model of the auditory nerve (AN) in combination with signal detection theory was used to test these assumptions. The underlying idea was that, for the BM compression to be estimated using psychoacoustics, enough information should be preserved at the level of the AN, because this forms an information bottleneck in the ascending auditory pathway. The simulated AN responses were quantified in terms of rate and synchrony for different types of AN fibers and CFs. The results show that, when using a low-intensity probe, local activity at the tonotopic location of the probe frequency is the dominant contributor to sensitivity in the healthy auditory system. However, on- and off-CF maskers produced similar forward masking onto the probe, which was mainly encoded by high- and to little extent by medium-spontaneous rate fibers. The simulation results suggested that the estimate of compression based on the behavioral experiments cannot be derived from sensitivity at the level of the AN but may require additional contributions, supporting previous physiological studies.


1996 ◽  
Vol 99 (4) ◽  
pp. 2543-2574 ◽  
Author(s):  
Christopher J. Plack ◽  
Andrew J. Oxenham

Author(s):  
R.J. Mount ◽  
R.V. Harrison

The sensory end organ of the ear, the organ of Corti, rests on a thin basilar membrane which lies between the bone of the central modiolus and the bony wall of the cochlea. In vivo, the organ of Corti is protected by the bony wall which totally surrounds it. In order to examine the sensory epithelium by scanning electron microscopy it is necessary to dissect away the protective bone and expose the region of interest (Fig. 1). This leaves the fragile organ of Corti susceptible to physical damage during subsequent handling. In our laboratory cochlear specimens, after dissection, are routinely prepared by the O-T- O-T-O technique, critical point dried and then lightly sputter coated with gold. This processing involves considerable specimen handling including several hours on a rotator during which the organ of Corti is at risk of being physically damaged. The following procedure uses low cost, readily available materials to hold the specimen during processing ,preventing physical damage while allowing an unhindered exchange of fluids.Following fixation, the cochlea is dehydrated to 70% ethanol then dissected under ethanol to prevent air drying. The holder is prepared by punching a hole in the flexible snap cap of a Wheaton vial with a paper hole punch. A small amount of two component epoxy putty is well mixed then pushed through the hole in the cap. The putty on the inner cap is formed into a “cup” to hold the specimen (Fig. 2), the putty on the outside is smoothed into a “button” to give good attachment even when the cap is flexed during handling (Fig. 3). The cap is submerged in the 70% ethanol, the bone at the base of the cochlea is seated into the cup and the sides of the cup squeezed with forceps to grip it (Fig.4). Several types of epoxy putty have been tried, most are either soluble in ethanol to some degree or do not set in ethanol. The only putty we find successful is “DUROtm MASTERMENDtm Epoxy Extra Strength Ribbon” (Loctite Corp., Cleveland, Ohio), this is a blue and yellow ribbon which is kneaded to form a green putty, it is available at many hardware stores.


1968 ◽  
Vol 11 (1) ◽  
pp. 63-76
Author(s):  
Donald C. Teas ◽  
Gretchen B. Henry

The distributions of instantaneous voltage amplitudes in the cochlear microphonic response recorded from a small segment along the basilar membrane are described by computing amplitude histograms. Comparisons are made between the distributions for noise and for those after the addition to the noise of successively stronger sinusoids. The amplitudes of the cochlear microphonic response to 5000 Hz low-pass noise are normally distributed in both Turn I and Turn III of the guinea pig’s cochlea. The spectral composition of the microphonic from Turn I and from Turn III resembles the output of band-pass filters set at about 4000 Hz, and about 500 Hz, respectively. The normal distribution of cochlear microphonic amplitudes for noise is systematically altered by increasing the strength of the added sinusoid. A decrease of three percent in the number of small amplitude events (±1 standard deviation) in the cochlear microphonic from Turn III is seen when the rms voltage of a 500 Hz sinusoid is at −18 dB re the rms voltage of the noise (at the earphone). When the rms of the sinusoid and noise are equal, the decrease in small voltages is about 25%, but there is also an increase in the number of large voltage amplitudes. Histograms were also computed for the output of an electronic filter with a pass-band similar to Turn III of the cochlea. Strong 500 Hz sinusoids showed a greater proportion of large amplitudes in the filter output than in CM III . The data are interpreted in terms of an anatomical substrate.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Haim Sohmer

The three modes of auditory stimulation (air, bone and soft tissue conduction) at threshold intensities are thought to share a common excitation mechanism: the stimuli induce passive displacements of the basilar membrane propagating from the base to the apex (slow mechanical traveling wave), which activate the outer hair cells, producing active displacements, which sum with the passive displacements. However, theoretical analyses and modeling of cochlear mechanics provide indications that the slow mechanical basilar membrane traveling wave may not be able to excite the cochlea at threshold intensities with the frequency discrimination observed. These analyses are complemented by several independent lines of research results supporting the notion that cochlear excitation at threshold may not involve a passive traveling wave, and the fast cochlear fluid pressures may directly activate the outer hair cells: opening of the sealed inner ear in patients undergoing cochlear implantation is not accompanied by threshold elevations to low frequency stimulation which would be expected to result from opening the cochlea, reducing cochlear impedance, altering hydrodynamics. The magnitude of the passive displacements at threshold is negligible. Isolated outer hair cells in fluid display tuned mechanical motility to fluid pressures which likely act on stretch sensitive ion channels in the walls of the cells. Vibrations delivered to soft tissue body sites elicit hearing. Thus, based on theoretical and experimental evidence, the common mechanism eliciting hearing during threshold stimulation by air, bone and soft tissue conduction may involve the fast-cochlear fluid pressures which directly activate the outer hair cells.


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