Home | About | Journals | Submit | Contact Us | Français |

**|**PLoS One**|**v.9(2); 2014**|**PMC3925081

Formats

Article sections

Authors

Related links

PLoS One. 2014; 9(2): e85969.

Published online 2014 February 14. doi: 10.1371/journal.pone.0085969

PMCID: PMC3925081

Manuel S. Malmierca, Editor^{}

University of Salamanca- Institute for Neuroscience of Castille and Leon and Medical School, Spain

* E-mail: vog.hin.xileh@kciwdahc

Conceived and designed the experiments: JL RC. Performed the experiments: JL. Analyzed the data: JL RC. Contributed reagents/materials/analysis tools: JL RC. Wrote the paper: JL RC.

Received 2013 September 25; Accepted 2013 December 9.

This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

This article has been cited by other articles in PMC.

Since Georg von Bekesy laid out the place theory of the hearing, researchers have been working to understand the remarkable properties of mammalian hearing. Because access to the cochlea is restricted in live animals, and important aspects of hearing are destroyed in dead ones, models play a key role in interpreting local measurements. Wentzel-Kramers-Brillouin (WKB) models are attractive because they are analytically tractable, appropriate to the oblong geometry of the cochlea, and can predict wave behavior over a large span of the cochlea. Interest in the role the tectorial membrane (TM) plays in cochlear tuning led us to develop models that directly interface the TM with the cochlear fluid. In this work we add an angled shear between the TM and reticular lamina (RL), which serves as an input to a nonlinear active force. This feature plus a novel combination of previous work gives us a model with TM-fluid interaction, TM-RL shear, a nonlinear active force and a second wave mode. The behavior we get leads to the conclusion the phase between the shear and basilar membrane (BM) vibration is critical for amplification. We show there is a transition in this phase that occurs at a frequency below the cutoff, which is strongly influenced by TM stiffness. We describe this mechanism of sharpened BM velocity profile, which demonstrates the importance of the TM in overall cochlear tuning and offers an explanation for the response characteristics of the Tectb mutant mouse.

Mammals transduce sound waves to neuronal signals within the fluid-filled cochlea via traveling waves in the organ of Corti (OC). This mechanical process is responsible for much of the extraordinary range and sensitivity that is characteristic of mammalian hearing, yet underlying mechanisms of nonlinear perception that enable the most interesting aspects of hearing, are still being determined [1], [27]. Investigators probe cochlear mechanics through a wide variety of methods, including velocimetry of the basilar membrane (BM) [3], multidirectional measurements of tectorial membrane (TM) motions [4], and recently measurements of the sensory epithelia, the reticular lamina (RL) [5]. However, these methods all offer glimpses of limited sections of the cochlea, so a well developed traveling wave model can help interpret the results. Sound manifests in the inner ear as a transverse traveling wave on the tissue of the OC. Mechanical frequency separation occurs via gradients in the mass and viscoelastic properties of the tissue that cause the position of peak vibration to depend on frequency. The precise mechanical structure of the mammalian cochlea has inspired many attempts to elucidate the roles of the different substructures through modeling. A useful way to examine the whole traveling wave is with a model based on the Wentzel-Kramers-Brillouin (WKB) approximation, a subset of perturbation theory ideal for analyzing waves propagating in slowly changing media. Originally, the approach was developed by using a simple, flexed basilar membrane (BM) to partition the cochlea fluid [6]. While outer hair cells (OHC) and their stereocilia are accepted as the primary source of nonlinearity, researchers continue to investigate the role other structural features have on the tuning curve. The tectorial membrane (TM) has been suggested as a possible source of secondary filtering or resonance [7], [8]. Previously, we increased the complexity of the cochlea WKB model by developing it with a modified “sandwich” cross-section [9], allowing the TM, which has a fluid-facing surface, to vibrate as a second degree of freedom and found that such a system can produce a second propagating wave [10]. However, this simple system did not include shear between the TM and RL, which must be an input for any amplification mechanisms involving OHCs [11]. Here, we expand that model and present an active dual wave model with three self-equilibrating degrees of freedom by including a shear motion at an angle set in the model. From this we see that relative phase of vibrating structures strongly affects active force output, enabling us to offer a novel explanation for observations of the Tectb mutant mouse [12]. We also consider longitudinal coupling within the tissue and the affect RL angle has on activity.

This model builds on results in [10], the aforementioned model where differential motion of the TM generates a second mode, and [13], which added a nonlinear active force onto a WKB-based model as a perturbation. The complete derivation of this model comprising aspects of both of these papers as well as the strategies discussed below, can be found in File S1. Here we focus on explaining the novel aspects of this work: the inclusion of the shear angle , between the RL and TM, and the active force perturbation worked out in the two wave system.

The cochlea is modeled as a long, fluid-filled duct partitioned into two compartments, the scala vestibule (SV) and scala tympani (ST), roughly corresponding to the physiology. The lumped masses, , and (subscripts indicating TM, RL and BM respectively) are proportional to cochlear width, *W(z)*, where *z* is the long dimension. This and other dimensions are based on observations for the mouse [14]. There are few measurements of viscoelastic properties in mice, and those that exist are difficult to interpret as single spring constants, so stiffness coefficients are based on the observed frequency range of a mouse, and increase from base to apex by a single exponential gradient. The ratio of damping to stiffness for the TM was determine from observations in [15] (rough calculations based on these moduli and the dimensions of the mouse TM suggest the stiffness values we use are of the correct order of magnitude.) Damping was otherwise kept small, increasing by an exponential coefficient that is half that for the stiffness (Tables S1 and S2 in File S1). We balance the internal forces of the OC with the fluid by considering the lumped-parameter cross section illustrated in Fig. 1, which defines most of the model viscoelastic and dimensional constants.

Some simplifying approximations specific to this model design are discussed as follows: by introducing the shear between the TM and RL we also introduce the possibility of two-dimensional motion the TM. Thin-film viscous adhesion will keep the gap between the TM and reticular lamina (RL) constant. The direction of the viscoelastic force due to the TM () varies such that it always works to restore the mass to its zero position. These approximations, and those in our previous work [19] lead to a tractable analytical model.

The partition equation relates the forces from the internal viscoelastic properties and displacements of the cochlear partition (CP) to the fluid pressure. These displacements are expressed using vector notation () where the subscripts denote the shear, upper, and basilar components respectively.

(1)

Here **M**, **D**, and **S** are slowly varying matrices describing respectively the internal mass, damping, and stiffness per unit length of the OC (Fig. 1 gives the subscript notation for each structure) and is a vector of fluid pressure at the partition (located at ). represents the active force, discussed below. Because all viscoelastic elements have mass and damping terms in parallel, the matrices **D** and **S** have the same form, and we represent them both with **V**. The cross section matrices and form of the pressure vector can be derived by balancing forces due to the elements of the CP and the forcing fluid pressure. The matrices are

(2)

(3)

To derive an analytical expression relating to , we recognize that the problem is one of multiple scales, where the cross section and wavelength dimensions are much shorter than the overall length of the cochlea. We thus use a WKB method to expand both quantities around the small number , where is the length of the cochlea, the ratio of the short to the long scales. We proceed to solve Laplace’s equation in both fluid chambers, using or the total displacement of the TM, , to describe the partition boundaries [10]. Combining this with the force balance in the cross section, the pressure term on the RHS of Eq. (1) becomes

(4)

where is the driving frequency, is the accumulated phase and is the wavenumber. The matrix is brackets will be shown as and

(5)

with being the fluid density. All of the solutions will have the form , where is … as appropriate.

Somatic electromotility in OHCs [16] implies the possibility of force applied between the RL and BM *in vivo*. The active force in this model is developed with this force profile and a standard sigmoid function, without further specifying the origin of the dominant nonlinearity. A Fourier coefficient is generated for the fundamental frequency and harmonics are neglected in the solution. The active force term can then be written as.

(6)

where is the Fourier coefficient defined as

(7)

and is the sigmoid function

(8)

The range of the function is scaled by the input saturation length, defined by the inverse of the sigmoid function . The output is normalized with the maximum force given explicitly by . To use the perturbation method in [13] we recognize that is much smaller than the scale of the inertial forces, i.e. . The ratio of the two gives a small number, , about which we expand and *k*. We also introduce the subscript notation to indicate the order the displacement after treated with the perturbation expansion. This gives us the homogeneous and perturbed equations

(9)

(10)

where the enumerated subscripts indicate expansion orders and is a coefficient dependent on that arises through the small number expansion and is expressed in File S1.

Eq. (9) represents the passive problem, which we solve as in [10] and then use the results to determine the active contribution. Briefly, this is a generalized eigenvalue problem for that can be solved computationally, using the WKB transport equation and the boundary conditions at the base to scale the eigenvectors. Although this model has three coupled equations, because is singular there are only two eigenmodes. The passive response of one mode is strongly influenced by the properties of the TM, and has larger amplitude on that structure, while the same can be said of the other and the BM, motivating the use of ^{} to denote each mode. Given this, the active system can be described via the expansions

(11)

(12)

Once the passive model is solved, we can use the resulting to calculate for each eigenmode. Eq. (10) is only solvable if the RHS is orthogonal to the eigenvector of the homogeneous equation, and from this solvability condition we can derive the expression for , the active wavenumber correction

(13)

The LHS of Eq. (10) requires choosing an eigenmode to set . Obviously the homogeneous solution will be the eigenvector for this mode; less obviously the particular solution will be the eigenvector of the other mode, which we need to scale. By assuming that the contribution from the homogeneous solution is entirely accounted for in the passive problem and setting it to 0, we can scale by solving Eq. (10). This involved expression is given in File S1.

We wished to consider the effect of longitudinal coupling in the TM, both to test the effect of a longitudinal coupling source besides the fluid on our model. We developed a term to be added to a two degree of freedom model, without any shear motion. represents longitudinal spring constants. A “waves on a string” problem typically involves taking two derivatives in the direction of wave propagation, in our model. However, in the WKB approximation we have employed, these derivatives are replaced by the wavenumber, we add the term

(14)

to the passive equation of motion. The active expansion derived in [13] cannot be worked with this term in place, but the passive model can still provide some insight.

Table 1 shows the zeroth order wavenumbers for the original passive model, that with added longitudinal coupling in the TM, and that with shear. The wavenumbers with large real and small imaginary components indicate propagating modes, and there are clearly two for each model. This is significant because neither the extra degree of freedom introduced by shearing, nor the additional longitudinal coupling added propagating waves. Previous works have dealt with evanescent wave modes, showing they make a perceptible contribution near the frequency cutoff [17], [18], or than they emerge with added components such as longitudinal coupling [19] and fluid chambers [20]. However, to our knowledge only another sandwich model [9] suggested an additional propagating mode is possible. We conclude the fluid-partition interfaces carry propagating modes like surface waves. This analysis demonstrates that only independent motions of the fluid-facing surfaces of the CP, the TM and BM create propagating waves. Since the CP is a viscoelastic structure, such independent motions could certainly arise *in vivo*, making the second wave an important consideration.

Also of note is the extreme similarity of wavenumbers between the system with and without shear. Adding this component lets us extract more information about the system, but the waves are essentially the same. Thus conclusions about the two degree of freedom system [10], including those regarding relative phases of the two modes and mode conversion, are valid as we increase model complexity.

The most significant result we found was that by increasing the stiffness of TM, the selectivity (as defined by the quality factor) of the BM increased, but the sensitivity (as defined by the maximum velocity) decreased, as shown in Table 2. Fig. 2 shows how the frequency responses of BM velocity and other quantities change with the TM stiffness. To maximize the impact of the active force we use an input SPL of 20 dB (referenced to 20 Pa, as is standard, and without modeling the middle ear transfer function, which likely adds some further gain [21].) We can see the decrease in quality factor corresponds to a shift in the region of significant gain. After testing the frequency of this transition against many model parameters, such as BM stiffness, OC stiffness, and TM damping (see File S1), we find it is strongly dependent on the TM stiffness and fairly insensitive to any other parameter examined.

The wavelength correction defined in Eq. (13) is responsible for most of the active force gain. Examining the equation analytically and looking at predictions for the frequency dependent behavior of the quantities on which depends do not reveal any dominating transitions that account for the sudden rise in gain, although several of them exhibit small bumps around the start of the gain. The model does predict a strong transition in the phase difference between the shearing motion and the basilar membrane vibration. Although the formula for does not explicitly involve this term, it is quite reasonable to expect the amplifier needs to work at a specific phase to the BM vibration to be effective. Indeed, Dong and Olson recently observed a transition the phase difference between the extracellular voltage of the *scala vestibuli*, which is related to the active force, and the fluid pressure near the BM, which indicates its motion [22]. They also suggest this phase shift optimizes the timing of the cochlear amplifier, and if one considers the phase of the active force should mimic the phase of the input shear, their result supports our prediction of a phase transition.

We can think of this transition as restricting the frequency range of the active region, somewhat akin to a high-pass filter. The abrupt loss of passive amplitude at the cutoff frequency restricts on the high-frequency end, together making a narrow band region of gain. Shifting the frequency of the “high-pass filter”, by changing the TM stiffness, but maintaining the frequency cutoff alters the Q of the frequency response. For stiffness values that allow the filtering effects to overlap, the frequency of maximum vibration is impacted by the gain-reducing qualities and is diminished, lowering sensitivity, trading sensitivity for selectivity. The high-frequency end of the band can be altered by varying BM stiffness, giving the same sensitivity-selectivity trade off (see File S1) but the frequency of the phase transition remains constant.

This result is particularly interesting given that velocity threshold measurements on the BM of the high-frequency (basal) region of the Tectb mutant mouse displays increased selectivity and somewhat decreased sensitivity compared to the wildtype [12]. The mutated protein is found extensively in the TM of this animal and the membrane, which at the base lacks an organized striated-sheet matrix and Hensen’s stripe, and is further disrupted at the apex. This TM phenotype and experiments [23] have led researchers to attribute the altered tuning curve to a decrease in longitudinal coupling associated with the loss of the striated-sheet matrix. It is suggested that OHCs on the periphery of the frequency place will be not be engaged in the mutant, leading to a decrease in overall amplification as well as finer tuning [24]. Modeling bears this out as a possible cause of fine tuning, but does not demonstrate decreased sensitivity [25]. Our result offers an alternate explanation, which can achieve the same phenomena based solely on changes in local resonance properties of the TM, without implicating longitudinal coupling.

As part of this interpretation, we must consider how the changes observed in the TM of the Tectb mutant may manifest themselves as the increase in stiffness required by our model. Our lumped stiffness parameter simultaneously represents TM attachment, elastic modulus, and any bending effects which are left out of our model. For modeling purposes we assumed a fairly homogeneous cross section, but the actual cochlea is quite complex, and any inhomogeneity due to fluid pressure, geometry or differential force from the cells versus the numerous fluid spaces in the OC may make the bending characteristics quite important. In this case, a loosely coupled system might in effect be stiffer by requiring a greater fluid pressure at some local point to produce the same amount of force transmitted at another local point (such as directly over the hair cells). Thus the observed disorganization of the TM structure that led other researchers to think about a decrease in longitudinal coupling might increase the lumped parameter spring constant.

To amplify BM vibrations, OHC electromotility must be properly timed in the vibration cycle [26]. Nilsen and Russel [27] discuss this and conclude amplification occurs at the maximum velocity of the OHC cycle, which occurs a quarter cycle after the maximum displacement. Chadwick [13] found a factor of *i* was needed for correct timing in his model. Examining Fig. 2, reveals the maximum gain in this model occurs when the RL displacement is nearly a quarter cycle different from the BM, corresponding to these experimental and model results.

In general, we assumed the phase of action of the cochlear amplifier was zero. That is, a positive shear of OHC stereocilia causes a contraction at the same point in the phase cycle without any sort of delay [28]. However, since *in vivo* factors including local damping from surrounding tissues and slow electrical response times may introduce delay, we investigated altering the phase of the input-output relation. The maximum velocity in these scenarios, shown in Fig. 3 is smaller, but interestingly the best frequency is also shifted. Even with no phase shift, our model shows peak activity at higher frequency than the passive velocity maximum, consistent with experiments that show the observed the best frequency shifts for very high input sound pressure levels (SPL) [29]. This suggests that phase differences in the amplifier could affect tuning as well as sensitivity.

By introducing the shear angle into the model, we gained a means to examine the role of this quantity which is known to grow from base to apex [14], [30]. While the angle has little effect on the passive BM vibration, a greater angle leads to much greater amplification as shown in Fig. 4. This is due to the larger shearing motion on the stereocilia, which is the input to the active force. Eq. (13) shows the wavenumber correction is directly proportional to this number. The larger angle couples more of the fluid force directed perpendicular to the partition into the shear direction, giving rise to a larger active force. Since this angle increases from base to apex, it may help aid amplification of low frequencies that must be carried far into the cochlea. This echoes work that suggests low frequency sound perception is enhanced at the apex by mechanics that selectively promote shear in this region [31].

Our model offers an intriguing possibility to explain the simultaneous increase in selectivity with loss of sensitivity of the Tectb mutant - a band pass filtering mechanism, with the low corner being determined by the TM-BM interaction. This idea lends further support to previous studies that suggest the properties of the TM are important to overall cochlear tuning [8], [32], [33] and specifically echoes work that suggests the TM-RL movement can act as a filtering mechanism [7], [11]. This work provides an in depth description of the mechanics, and adds nonlinear cochlear activity.

There is a the growing body of evidence that the TM is a critical structure in the precise nature of mammalian hearing [34], especially frequency filtering. Working with the TM in isolation can provide valuable insight into its mechanical properties, though we emphasize that the results we get with this model require the components be assembled as a system. We have demonstrated that TM properties affect a transition in the phase of the hair bundle shear that limits the effectiveness of OHCs in amplifying BM vibrations at low frequencies, increasing selectivity.

**Figure S1, Frequency responses due to change in TM damping.** More TM damping leads to a smoother curve, but does not significantly shift the peak or the frequencies of the phase transition. Sensitivity increases with selectivity. **Figure S2, Frequency responses due to change in OC stiffness.** In this case, increased coupling between the TM and BM leads to a sharper, bumpier curve, and sensitivity increases with selectivity. **Figure S3, Frequency responses due to change in BM stiffness.** Changing the BM stiffness leads to a trade in sensitivity for selectivity. In this case, we can observe that the peak frequency increases with BM stiffness, as expected, while the phase difference remains the same. This is compatible with our band pass filter description of the tuning mechanism, but in this case we are moving the high frequency corner. **Figure S4, Diagram of the three masses of the cochlear partition and the forces on them per unit length.** Arrows are intended to depict direction of force due to positive displacements. The direction of depends on TM position. **Table S1, Viscoelastic Parameters. Table S2, Structural Dimensions.**

(PDF)

Click here for additional data file.^{(217K, pdf)}

We would like to thank D. Manoussaki for her advice on certain mathematical points, and for critical comments. We also thank S. Smith for critical comments.

This work was supported by the intramural program project DC00033 in the National Institute on Deafness and other Communication Disorders. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

1. Ashmore J (2008) Cochlear outer hair cell motility. Physiol Rev 88: 173–210 [PubMed]

2. Hudspeth AJ (2008) Making an effort to listen: mechanical amplification in the ear. Neuron 59: 530–45 [PMC free article] [PubMed]

3. Ruggero MA, Rich NC, Recio A, Narayan SS, Robles L (1997) Basilar-membrane responses to tones at the base of the chinchilla cochlea. J Acoust Soc Am 101: 2151–2163 [PMC free article] [PubMed]

4. Hemmert W, Zenner HP, Gummer AW (2000) Three-dimensional motion of the organ of corti. Biophys J 78: 2285–97 [PubMed]

5. Chen F, Zha D, Fridberger A, Zheng J, Choudhury N, et al. (2011) A differentially amplified motion in the ear for near-threshold sound detection. Nat Neurosci 14: 770–4 [PMC free article] [PubMed]

6. Steele CR, Taber LA (1979) Comparison of wkb and finite difference calculations for a two-dimensional cochlear model. J Acoust Soc Am 65: 1001–6 [PubMed]

7. Allen JB (1980) Cochlear micromechanics-a physical model of transduction. J Acoust Soc Am 68: 1660–70 [PubMed]

8. Ghaffari R, Aranyosi AJ, Freeman DM (2007) Longitudinally propagating traveling waves of the mammalian tectorial membrane. Proc Natl Acad Sci USA 104: 16510–5 [PubMed]

9. de Boer E (1990) Wave-propagation modes and boundary conditions for the Ulfendahl-Flock-Khanna preparation. In: Dallos P, Geisler CD, Matthews JW, Ruggero MA, Steele CR, editors, The Mechanics and Biophysics of Hearing, Berlin: Springer-Verlag. 333–339.

10. Lamb JS, Chadwick RS (2011) Dual traveling waves in an inner ear model with two degrees of freedom. Phys Rev Lett 107: 088101. [PMC free article] [PubMed]

11. Zwislocki JJ, Kletsky EJ (1979) Tectorial membrane: a possible effect on frequency analysis in the cochlea. Science 204: 639–41 [PubMed]

12. Russell IJ, Legan PK, Lukashkina VA, Lukashkin AN, Goodyear RJ, et al. (2007) Sharpened cochlear tuning in a mouse with a genetically modified tectorial membrane. Nat Neurosci 10: 215–23 [PMC free article] [PubMed]

13. Chadwick RS (1998) Compression, gain, and nonlinear distortion in an active cochlear model with subpartitions. Proc Natl Acad Sci USA 95: 14594–9 [PubMed]

14. Keiler S, Richter CP (2001) Cochlear dimensions obtained in hemicochleae of four different strains of mice: Cba/caj, 129/cd1, 129/svev and c57bl/6j. Hear Res 162: 91–104 [PubMed]

15. Gavara N, Chadwick R (2010) Noncontact microrheology at acoustic frequencies using frequency-modulated atomic force microscopy. Nature Methods 8: 650–4 [PMC free article] [PubMed]

16. Brownell WE, Bader CR, Bertrand D, de Ribaupierre Y (1985) Evoked mechanical responses of isolated cochlear outer hair cells. Science 227: 194–6 [PubMed]

17. Elliott SJ, Ni G, Mace BR, Lineton B (2013) A wave finite element analysis of the passive cochlea. The Journal of the Acoustical Society of America 133: 1535–1545 [PubMed]

18. Watts L (2000) The mode-coupling liouville-green approximation for a two-dimensional cochlear model. J Acoust Soc Am 108: 2266–71 [PubMed]

19. Elliott S, Ni G, Mace B, Lineton B (2011) How many waves propagate in the cochlea? In: AIP Conference Proceedings. volume 1403, p. 563.

20. Chadwick RS, Dimitriadis EK, Iwasa KH (1996) Active control of waves in a cochlear model with subpartitions. Proc Natl Acad Sci USA 93: 2564–9 [PubMed]

21. Saunders JC, Summers RM (1982) Auditory structure and function in mouse middle ear: an evaluation by sem and capacitive probe. J Comp Physiol 146: 517–25

22. Dong W, Olson ES (2013) Detection of cochlear amplification and its activation. Biophys J 105: 1067–78 [PubMed]

23. Ghaffari R, Aranyosi AJ, Richardson GP, Freeman DM (2010) Tectorial membrane travelling waves underlie abnormal hearing in tectb mutant mice. Nat Commun 1: 96. [PMC free article] [PubMed]

24. Lukashkin AN, Richardson GP, Russell IJ (2010) Multiple roles for the tectorial membrane in the active cochlea. Hear Res 266: 26–35 [PubMed]

25. Meaud J, Grosh K (2010) The effect of tectorial membrane and basilar membrane longitudinal coupling in cochlear mechanics. J Acoust Soc Am 127: 1411–21 [PubMed]

26. Russell IJ, Kossl M (1992) Sensory transduction and frequency selectivity int the basal turn of the guinea-pig cochlea. Phil Trans R Soc Lond B 336: 317–24 [PubMed]

27. Nilsen KE, Russell IJ (2000) The spatial and temporal representation of a tone on the guinea pig basilar membrane. Proc Natl Acad Sci USA 97: 11751–8 [PubMed]

28. Santos-Sacchi J (1992) On the frequency limit and phase of outer hair cell motility: effects of the membrane filter. J Neurosci 12: 1906–16 [PubMed]

29. Robles L, Ruggero MA (2001) Mechanics of the mammalian cochlea. Physiol Rev 81: 1305–52 [PMC free article] [PubMed]

30. Dallos P, Popper AN, Fay RR (1996) The Cochlea, volume 8 of Springer handbook of auditory research. New York: Springer.

31. Manoussaki D, Chadwick RS, Ketten DR, Arruda J, Dimitriadis EK, et al. (2008) The inuence of cochlear shape on low-frequency hearing. Proc Natl Acad Sci USA 105: 6162–6 [PubMed]

32. Allen JB, Fahey PF (1993) A second cochlear-frequency map that correlates distortion product and neural tuning measurements. J Acoust Soc Am 94: 809–16 [PubMed]

33. Zwislocki JJ (1986) Analysis of cochlear mechanics. Hear Res 22: 155–69 [PubMed]

34. Richardson GP, Lukashkin AN, Russell IJ (2008) The tectorial membrane: one slice of a complex cochlear sandwich. Curr Opin Otolaryngol Head Neck Surg 16: 458–64 [PMC free article] [PubMed]

Articles from PLoS ONE are provided here courtesy of **Public Library of Science**

PubMed Central Canada is a service of the Canadian Institutes of Health Research (CIHR) working in partnership with the National Research Council's national science library in cooperation with the National Center for Biotechnology Information at the U.S. National Library of Medicine(NCBI/NLM). It includes content provided to the PubMed Central International archive by participating publishers. |