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Published in: Journal of the Association for Research in Otolaryngology 2/2024

Open Access 26-02-2024 | Review

Swept Along: Measuring Otoacoustic Emissions Using Continuously Varying Stimuli

Author: Christopher A. Shera

Published in: Journal of the Association for Research in Otolaryngology | Issue 2/2024

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Abstract

At the 2004 Midwinter Meeting of the Association for Research in Otolaryngology, Glenis Long and her colleagues introduced a method for measuring distortion-product otoacoustic emissions (DPOAEs) using primary-tone stimuli whose instantaneous frequencies vary continuously with time. In contrast to standard OAE measurement methods, in which emissions are measured in the sinusoidal steady state using discrete tones of well-defined frequency, the swept-tone method sweeps across frequency, often at rates exceeding 1 oct/s. The resulting response waveforms are then analyzed using an appropriate filter (e.g., by least-squares fitting). Although introduced as a convenient way of studying DPOAE fine structure by separating the total OAE into distortion and reflection components, the swept-tone method has since been extended to stimulus-frequency emissions and has proved an efficient and valuable tool for probing cochlear mechanics. One day—a long time coming—swept tones may even find their way into the audiology clinic.
Appendix
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Footnotes
1
At the same 2004 Midwinter Meeting of the ARO during which swept-tone DPOAEs made their debut [5], and presented almost side-by-side, just two posters down the aisle, Stephen Neely and his colleagues described a method for continuously varying the primary levels [68].
 
2
To appreciate the depth of the times involved, note that the scale along the abscissa in Fig. 4 indicates how twice the expected SNR for a synchronous averaging task varies with the measurement time. Thus, relative to the SNR achieved during the first year, measuring a sinusoid embedded in Gaussian noise for the full 65 million years since the K-T extinction lowers the noise floor by some \(\frac{1}{2}20\log _{10}(65) = 78\,\) dB.
 
3
Although echolocation evolved multiple times on Earth—not only in bats but also in toothed whales (e.g., dolphins), as well as in shrews and tenrecs [18], oilbirds and swiftlets [19], and some blind humans [20]—only laryngeal bats employ frequency-modulated, chirp-like signals rather than acoustic clicks.
 
4
To estimate the group velocity of the traveling wave, we approximate both the BM frequency response (\(\textrm{TF}\)) and the traveling-wave envelope (\(\textrm{TW}\)) as Gaussians of widths \(\sigma _f\) and \(\sigma _x\), respectively. Thus, \(\textrm{TF}= \exp [-\frac{1}{2}((f-\textrm{CF})/\sigma _f)^2]\) and \(\textrm{TW}= \exp [-\frac{1}{2}((x-\hat{x})/\sigma _x)^2]\), where \(\textrm{CF}\) is the characteristic frequency and \(\hat{x}\) is the best place (peak of the wave). When the cochlear tonotopic map is exponential, the widths \(\sigma _f\) and \(\sigma _x\) are related by \(\sigma _x=(\ell /\textrm{CF})\sigma _f\), where \(\ell\) is the exponential space constant of the map. The equivalent rectangular bandwidth (\(\textrm{ERB}\)) of the Gaussian filter is given by \(\textrm{ERB}=\sqrt{\pi }\sigma _f\). We approximate the group velocity at the peak of the traveling wave by \(v_\textrm{g}\approx \Delta x/\tau\), where \(\Delta x\) is the effective width of the peak region and \(\tau\) is the wave travel time across this region. Since OAE latency is dominated by round-trip delays within the peak region, we approximate \(\tau\) as \(\tau \approx \frac{1}{2}\tau _\textrm{SFE}\), where \(\tau _\textrm{SFE}\) is SFOAE group delay. Approximating the width of the scattering region as \(\Delta x\approx 4\sigma _x\), we have \(\Delta x\approx 4\ell \sigma _f/\textrm{CF}= 4\ell /(\sqrt{\pi }Q_{\textrm{ERB}})\), where \(Q_{\textrm{ERB}}=\textrm{CF}/\textrm{ERB}\). Putting it all together yields \(v_\textrm{g}=8\ell \textrm{CF}/(\sqrt{\pi }N_\textrm{SFE}Q_{\textrm{ERB}})\), where \(N_\textrm{SFE}=\tau _\textrm{SFE}\textrm{CF}\) is SFOAE delay in stimulus periods. Relating \(N_\textrm{SFE}\) and \(Q_{\textrm{ERB}}\) using the tuning ratio (\(Q_{\textrm{ERB}}=rN_\textrm{SFE}\)) yields \(v_\textrm{g}=8\ell \textrm{CF}/(\sqrt{\pi }rN_\textrm{SFE}^2)\). To relate this velocity to sweep rates it is convenient to express \(v_\textrm{g}\) in octaves/s (rather than, say mm/s). For this, we use the relation \(\Delta x_\textrm{oct}=\Delta x/(\ell \ln 2)\). Hence, \(v_\textrm{g}=8\textrm{CF}/(\sqrt{\pi }\ln 2\,rN_\textrm{SFE}^2)\) (oct/s). Figure 5 is computed using published human SFOAE delays [29] and averaged tuning ratios for cat, guinea pig, and chinchilla [30, 31].
 
5
The figure shows human DPOAE data. In common laboratory animals, correlation bandwidths are typically a factor of 2 or 3 larger. This is true not only because animal DPOAE fine-structure patterns vary more slowly with frequency (since their OAE delays are shorter than those of humans [54]), but also because the peak-to-peak amplitude of the fine-structure oscillations is generally also reduced.
 
6
For a fixed SNR, the potential reduction in measurement time depends on the desired frequency resolution of the measurement. If this resolution is \(\Delta f\) and the chosen analysis bandwidth is \(\textrm{BW}\) (with \(\textrm{BW}>\Delta f\)), then the use of swept tones can speed up the total measurement by roughly a factor of \(\frac{1}{2}(\textrm{BW}/\Delta f)\). If \(\Delta f>\frac{1}{2}\textrm{BW}\) then one may be better off using discrete tones.
 
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Metadata
Title
Swept Along: Measuring Otoacoustic Emissions Using Continuously Varying Stimuli
Author
Christopher A. Shera
Publication date
26-02-2024
Publisher
Springer US
Published in
Journal of the Association for Research in Otolaryngology / Issue 2/2024
Print ISSN: 1525-3961
Electronic ISSN: 1438-7573
DOI
https://doi.org/10.1007/s10162-024-00934-5

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