Abstract:In order to better understand signal propagation in the ear, a time-domain model of the tympanic membrane (TM) and of the ossicular chain (OC) is derived for the cat. Ossicles are represented by a two-port network and the TM is discretized into a series of transmission lines, each one characterized by its own delay and reflection coefficient. Volume velocity samples are distributed along the ear canal, the eardrum, and the middle ear, and are updated periodically to simulate wave propagation. The interest of t… Show more
“…The 14-ms value derived from human subjects is very close to the value that we obtained from the guinea-pig model. In differences between the expected and observed values in guinea pig can be accounted for by interspecies differences in propagation speed, which in turn depends on TM curvature, inclination to the ear canal and material anisotropy (Fay et al, 2006;Parent and Allen, 2007). With respect to the second assertion, it is clearly incorrect to equate one-way propagation delay in the forward direction to overall propagation delay in the forward direction (Parent and Allen, 2010).…”
Section: Propagation Delay Of the Tympanic Membranementioning
confidence: 85%
“…In contrast to guinea pig (Sec. 3.3), for human C B [5.5 mF in Zwislocki (1962)] is larger than the acoustic compliances of the malleus (0.32 mF) and annular ligament (0.16 mF), both calculated from Parent and Allen (2007). 9 Therefore, pathological changes in C M and/or C C are expected to be detectable in f-TF.…”
Section: Differential Diagnosis Of Conductive and Sensorineural Hearimentioning
“…The 14-ms value derived from human subjects is very close to the value that we obtained from the guinea-pig model. In differences between the expected and observed values in guinea pig can be accounted for by interspecies differences in propagation speed, which in turn depends on TM curvature, inclination to the ear canal and material anisotropy (Fay et al, 2006;Parent and Allen, 2007). With respect to the second assertion, it is clearly incorrect to equate one-way propagation delay in the forward direction to overall propagation delay in the forward direction (Parent and Allen, 2010).…”
Section: Propagation Delay Of the Tympanic Membranementioning
confidence: 85%
“…In contrast to guinea pig (Sec. 3.3), for human C B [5.5 mF in Zwislocki (1962)] is larger than the acoustic compliances of the malleus (0.32 mF) and annular ligament (0.16 mF), both calculated from Parent and Allen (2007). 9 Therefore, pathological changes in C M and/or C C are expected to be detectable in f-TF.…”
Section: Differential Diagnosis Of Conductive and Sensorineural Hearimentioning
“…While the overall bullfrog TyM motion is complex, we propose a relatively simple model to capture its essential features. Consider the TyM as a distributed segment of transmission line (e.g., [12]) connecting the air to the ossicles (and subsequently the inner ear). At frequencies where the characteristic impedance of the transition (i.e., air-to-TyM, TyM-to-ossicle) is well-matched, a slow-traveling wave behavior will dominate.…”
Abstract. Several studies have demonstrated that delays associated with evoked otoacoustic emissions (OAEs) largely originate from filter delays of resonant elements in the inner ear. However, one vertebrate group is an exception: Anuran (frogs and toads) amphibian OAEs exhibit relatively long delays (several milliseconds), yet relatively broad tuning. These delays, also apparent in auditory nerve fiber (ANF) responses, have been partially attributed to the middle ear (ME), with a total forward delay of ∼0.7 ms (∼30 times longer than in gerbil). However, ME forward delays only partially account for the longer delays of OAEs and ANF responses. We used scanning laser Doppler vibrometery to map surface velocity over the tympanic membrane (TyM) of anesthetized bullfrogs (Rana catesbeiana). Our main finding is a circularly-symmetric wave on the TyM surface, starting at the outer edges of the TyM and propagating inward towards the center (the site of the ossicular attachment). This wave exists for frequencies ∼0.75-3 kHz, overlapping the range of bullfrog hearing (∼0.05-1.7 kHz). Group delays associated with this wave varied from 0.4 to 1.2 ms and correlated with with TyM diameter, which ranged from ∼6-16 mm. These delays correspond well to those from previous ME measurements. Presumably the TyM waves stem from biomechanical constraints of semi-aquatic species with a relatively large tympanum. We investigated some of these constraints by measuring the pressure ratio across the TyM (∼10-30 dB drop, delay of ∼0.35 ms), the effects of ossicular interruption, the changes due to physiological state of TyM ('dry-out'), and by calculating the middle-ear input impedance. In summary, we found a slow, inward-traveling wave on the TyM surface that accounts for a substantial fraction of the relatively long otoacoustic and neurophysiological delays previously observed in the anuran inner ear.
“…Previous studies of the acoustic input impedance of the ear include lumped element models of the human middle ear (e.g., Kringlebotn 1988;Moller 1961;Zwislocki 1962), experimental studies of the middle ear of human temporal bones (e.g., O'Connor and Puria 2008;Voss et al 2000), experimental studies of human ears (e.g., Farmer-Fedor and Rabbitt 2002;Kringlebotn 1994;Margolis et al 1999;Moller 1965;Rabinowitz 1981;Voss and Allen 1994), and models and experimental studies of animal ears (e.g., Huang et al 2000;Lynch et al 1994;Parent and Allen 2007). Prior to 1981, experimental studies of the acoustic input impedance of the ear in humans were limited to about 1.5 kHz, the ear canal treated as an acoustic compliance (Rabinowitz 1981).…”
Ear canal acoustics was examined using a onedimensional lossy transmission line with a distributed load impedance to model the ear. The acoustic input impedance of the ear was derived from sound pressure measurements in the ear canal of healthy human ears. A nonlinear least squares fit of the model to data generated estimates for ear canal radius, ear canal length, and quantified the resistance that would produce transmission losses. Derivation of ear canal radius has application to quantifying the impedance mismatch at the eardrum between the ear canal and the middle ear. The length of the ear canal was found, in general, to be longer than the length derived from the one-quarter wavelength standing wave frequency, consistent with the middle ear being mass-controlled at the standing wave frequency. Viscothermal losses in the ear canal, in some cases, may exceed that attributable to a smooth rigid wall. Resistance in the middle ear was found to contribute significantly to the total resistance. In effect, this analysis "reverse engineers" physical parameters of the ear from sound pressure measurements in the ear canal.
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