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Article
Manipulating the Hardness of HATS-Mounted Ear Pinna
Simulators to Reproduce Cartilage Sound Conduction
Ryota Shimokura 1, *, Tadashi Nishimura 2 and Hiroshi Hosoi 3
Abstract: Although hearing devices based on cartilage conduction have become more widely used
in Japan, methods for evaluating the output volume of such devices have not yet been established.
Although the output of air-conduction-based sound-generating devices (e.g., earphones and hearing
aids) can be standardized via the head and torso simulator (HATS), this is not applicable to cartilage
conduction devices because the simulated pinna is too soft (hardness: A5) compared with human
aural cartilage. In this study, we developed polyurethane pinna that had the same shape but different
degrees of hardness (A40, A20, and A10). We then compared the HATS results for the new pinna
simulators with data from human ears. We found that the spectral shapes of the outputs increasingly
approximated those of human ears as the simulated pinna hardness decreased. When a durometer
was pressed against the ear tragus of a human ear, the hardness value ranged from A10 to A20.
Accordingly, cartilage-conduction-based sound information could be obtained using a HATS that
had a simulated pinna with a similar hardness value.
Citation: Shimokura, R.; Nishimura, Keywords: cartilage conduction; pinna simulator; head-and-torso simulator (HATS); hearing aid;
T.; Hosoi, H. Manipulating the sound pressure level
Hardness of HATS-Mounted Ear
Pinna Simulators to Reproduce
Cartilage Sound Conduction. Appl.
Sci. 2022, 12, 12532. https://doi.org/ 1. Introduction
10.3390/app122412532
Aural cartilage gives form to the pinna and the exterior half of the external auditory
Academic Editor: Theodore E. canal. When a transducer is pressed against the pinna, the cartilage acts as a diaphragm and
Matikas produces sound in the external auditory canal [1,2]. The generated sounds and propagated
Received: 9 November 2022
vibrations that arise when a transducer is applied to the ear lobe (adipose tissue) and
Accepted: 6 December 2022
temporal bone are weaker than those at the tragus, scaphoid fossa, and concha because
Published: 7 December 2022
these latter structures contain cartilage [3,4]. As a result, this sound pathway is termed
cartilage conduction [2–9]. Hearing devices based on cartilage conduction (e.g., hearing
Publisher’s Note: MDPI stays neutral
aids [10] and earphones [11]) are currently being marketed in Japan. Although cartilage
with regard to jurisdictional claims in
conduction and bone conduction are both realized by touching a transducer to the user’s
published maps and institutional affil-
body, the vibrations that propagate through the skull bone when cartilage is stimulated are
iations.
sufficiently small to disregard the contribution of hearing perception [6].
Although cartilage-conduction-based devices are widely used, there are no standard-
ized procedures or indicators for measuring the output volumes of such devices. Because
Copyright: © 2022 by the authors.
the transmission pathway of cartilage conduction differs from those of air and bone con-
Licensee MDPI, Basel, Switzerland. duction, the calibration methods of the International Organization for Standardization
This article is an open access article (air conduction [12] and bone conduction [13]) do not apply to cartilage-conduction-based
distributed under the terms and devices. For example, for bone conduction, an artificial mastoid (Type 4130; Brüel & Kjaer,
conditions of the Creative Commons Naerum, Denmark) is used to simulate the mechanical impedance of the human mas-
Attribution (CC BY) license (https:// toid [14]. The output of an artificial mastoid can be calibrated by pressing a transducer onto
creativecommons.org/licenses/by/ the mastoid sensor with a force of 1 N. However, an artificial mastoid is unfit for monitoring
4.0/). sound in the external auditory canal because it does not include a pinna simulator.
To measure air conduction, the sound pressure at the ear drum can be simulated using
a pinna simulator [15] embedded in a head-and-torso simulator (HATS) [16]. However, the
output from the HATS is different from that obtained in the human external auditory canal
by inserting a probe microphone in it, even if the same transducer is used to stimulate the
ear at the same position. For instance, when a ring-shaped transducer was placed on the en-
trance of the external auditory canal, the sound pressure levels (SPLs) in the canal disagreed
with those obtained using the HATS, especially in the low-frequency range, i.e., below
1.5 kHz (see Figure 1a) [17]. However, we found that a soft polyurethane pipe attached to a
skull bone model could be used to simulate the aural cartilage of the external auditory canal
and that this arrangement was able to produce an SPL that was consistent with data from
human ears at this low-frequency range (Figure 1b). Polyurethane resin was used to mimic
the elasticity of human skin (human skin gel, Exseal Corporation, Mino, Japan). In contrast,
the pinna simulator in the HATS (Type 4128; Brüel & Kjaer, Naerum, Denmark) is em-
bedded as a unit in a silicon rubber base (width × height × thickness: 50 × 60 × 10 mm3 ),
and the hardness (Shore 00 35 or Shore A5 from durometer measurements) is lower than
that of human aural cartilage.
Figure 1. Simulated cartilage conduction sound (solid line) obtained in the (a) HATS and (b) model
aural cartilage. The dashed lines indicate the measured cartilage-conduction sound obtained from
the participants. The SPLs obtained in the human canal and by the HATS disagreed, especially in the
low-frequency range below 1.5 kHz.
The hardness of the pinna simulator in the HATS is likely to be an important variable
in accurately simulating the cartilage conduction sound. Therefore, our research group
examined the generated cartilage-conduction sound in five ear simulators, each made
of silicon rubber with a different hardness [18]. The ear simulators included the pinna
and external auditory canal, and the cartilage-conduction sounds were measured via a
probe microphone (type 4182; Brüel & Kjaer, Naerum, Denmark) inserted into the canal.
Our results indicated that the spectral characteristics of the cartilage-conduction sounds
recorded from the ear simulators approached those from human ears when the hardness of
the simulators coincided with that of human aural cartilage (Shore A10 to A20). Accordingly,
in the present study, we made HATS-mounted pinna simulators with three different
hardness levels and measured the cartilage-conduction sounds. We expect that because
the HATS is used in most medical institutes to calibrate normal hearing aids, the ability
to upgrade the device by exchanging only the pinna simulator would be convenient for
healthcare professionals.
Appl. Sci. 2022, 12, 12532 3 of 8
2. Method
2.1. Pinna Simulators
The pinna simulator is made of silicon rubber (Shore 00 35 or Shore A5) and can
be easily attached to or removed from the HATS (base: width × height × thickness:
50 × 60 × 10 mm3 ) via a magnetic backing component. The silicon base has a canal with a
diameter of 5 mm and is colinear with respect to the end of the ear canal. The ear canal
ends in an occluded ear simulator, which simulates the inner part of the ear canal according
to the International Electrotechnical Commission (IEC 60318-4) [16]. The ear simulator
contains a half-inch microphone that can be connected to a microphone preamplifier using
an adaptor.
We removed the pinna simulator from the HATS and made a mold, which enabled us
to make new pinna simulators with three different hardness levels (A40, A20, and A10), as
shown in Figure 2a. We used polyurethane resin because the human skin gel, described
above, was made of this material [17]. Although the original pinna simulator in the HATS
(original HATS pinna after that) had a concavo-convex surface on the reverse side of the
base where it joined with the HATS body, the new pinna simulator had a flat surface.
Furthermore, the new pinna simulators did not have a magnet to join them to the HATS.
Thus, we used rubber cement (Blu Tack, Bostik Australia Pty. Ltd., Thomastown, Australia)
to fix and fill the gaps between the pinna simulator and the HATS body. The masses of the
pinna simulators were 42 g for A40, 44 g for A20, 48 g for A10, and 49 g for the original
HATS pinna.
Figure 2. (a) Developed pinna simulators (A10, A20, and A40 from the left) and (b) embedded pinna
simulator in the HATS and position of the cartilage conduction transducer at the entrance of the
external auditory canal.
Appl. Sci. 2022, 12, 12532 4 of 8
3. Results
Figure 3 shows the SPLs obtained for the HATS according to the hardness of the
pinna simulators and the SPLs obtained for human ears. To ensure the repeatability of our
method, we attached the transducers to the HATS and removed them three times, as shown
by solid lines (the averaged values) in the figure. The dashed lines indicate the average
values from three human participants in a previous study [6].
In the human cartilage-conduction sound data (dashed line), the spectral peak around
2.5 kHz is caused by resonance in the external auditory canal, while the peak around 800 Hz
is specifically associated with cartilage conduction [6]. Although the lower peak was too
sharp for the original HATS pinna, as shown in Figure 3d, the urethane pinna simulators in
the present study produced close spectral shapes that were lower than 1 kHz. Particularly,
when the hardness of the pinna simulator approached that of human aural cartilage (A10
to A20), the spectral shapes became more similar to the dashed line representing the
human data (Figure 3b,c). In contrast, for frequencies higher than 5 kHz, we observed
large differences in cartilage conduction between the HATS and human measurements,
regardless of the pinna hardness. The averaged errors between the conduction sounds
generated by the simulator (solid line) and human cartilage (dashed line) were 6.9 dB for
A40, 6.4 dB for A20, 4.8 dB for A10, and 4.8 dB for the original HATS pinna in the frequency
range below 5 kHz. Although the original HATS pinna showed a different spectral shape,
the averaged error was close to the A10.
Appl. Sci. 2022, 12, 12532 5 of 8
Figure 3. Simulated cartilage-conduction sound obtained by the HATS with different pinna simula-
tors: (a) A40, (b) A20, (c) A10, and (d) original silicon-rubber-based HATS pinna simulator (solid line).
The dashed lines indicate the measured cartilage-conduction sound obtained from the participants.
The spectral shapes of A10 and A20 became more similar to those obtained from the participants.
4. Discussion
Consistent with previous findings [18], the cartilage-conduction peak (around 800 Hz)
of the pinna simulator approached that of human aural cartilage when the hardness of the
pinna simulator was A20 or A10 (Figure 3). Unlike the previous simulation study that used
a polyurethane pipe [17], the resonance peak in the external auditory canal (around 2.5 kHz)
in the present study was closer to that of a human ear because of the more precise pinna
shape (see Figure 1b). The frequencies of the HATS at the maximum peak below 1 kHz were
1 kHz for A40, 841 Hz for A20, and 841 Hz for A10, while that for a human ear was 749 Hz.
In a previous study [18], these frequencies were 1414 Hz for A40, 1 kHz for A20, and 561 Hz
for A10. The previous [18] and current pinna simulators were made out of silicon rubber
and polyurethane resin, respectively, so dissimilarities in the physical properties might
have created the differences in peak frequencies. If the cartilage-conduction peak is shifted
toward the lower-frequency range (Figure 3c), the outputs from the pinna simulators and
real ears can be more closely approximated for sounds below this peak.
The durometer value can be applied to Young’s modulus using the following equation:
0.0981(56 + 7.62336S)
E= (1)
0.137505(254 − 2.54S)
where E is Young’s modulus [Mpa] and S is a type A durometer hardness [19]. This
equation is considered a good first-order approximation of Young’s modulus for type A
Appl. Sci. 2022, 12, 12532 6 of 8
hardness, especially from A20 to A80. Based on this equation, the Young’s moduli of
the pinna simulators were 1.69 Mpa for A40, 0.73 Mpa for A20, 0.41 Mpa for A10, and
0.28 Mpa for the original HATS pinna. Although Young’s moduli are often measured
in research on auricular reconstructions, the values differ according to the measurement
equipment and procedure. For cadaveric auricular cartilage dissected from the skin and
fascia, the measured Young’s moduli were 5.02 Mpa in [20] and 1.41 to 2.08 Mpa in [21]. To
simulate sound transmission numerically through an ear-filling earplug, Weinmann et al.
assigned Young’s moduli to each type of tissue that makes up the pinna: 0.65 Mpa for skin,
0.001 Mpa for fat, 0.79 Mpa for muscle, 13.6 Mpa for bone, and 1.9 Mpa for cartilage [22].
According to this classification, the A20 and A10 correspond to the skin or muscle. In the
previous study, the hardness of human aural cartilage was measured using a durometer
(GS-719N; Teclock, Nagano, Japan) [18]. The pointed cylinder of the durometer was pressed
against the ear tragus and was allowed to inflect the tragus during the measurement. In
this case, the pointed cylinder directly contacted the skin over the cartilage, and so the
measured hardness might be lower than the hardness of the singular aural cartilage. In
hardness measurements that limited the displacement of the pinna, the hardness of the
ear helix ranged from A25 to A55 according to individual differences [23]. The numerical
simulations conducted by Weinman et al. revealed that the vibrations at the points of the
pinna might be propagated via the surface of the skin [22]. However, stimulation at the ear
lobe (adipose tissue) did not effectively propagate vibrations on the pinna, even though the
ear lobe is also covered by skin [3]. Furthermore, vibrations were not propagated through
the osseous part of the external auditory canal even though this bone is covered by skin [8].
According to these data, the layer construction of the skin and the aural cartilage appear to
facilitate vibrational propagation.
For frequencies higher than 5 kHz, the pinna simulators showed a large gap with
respect to the output of the human ear, regardless of the material hardness (Figure 3a–c).
Although such a high-frequency range is not so essential for the output evaluation of a
hearing aid aimed at speech recognition [24,25], the gap cannot be ignored for listening
to music via the cartilage-conduction devices. The original HATS pinna had a concavo-
convex surface on the base where it attached to the body of the HATS. In contrast, our
new pinna simulators had a flat surface on the base. As a result, there was a narrow
clearance with respect to the HATS device, although we tried to fill this space with rubber
cement. Resonance in the remaining cavity might explain the difference in the output
between the pinna simulator and real human ears. In further study, we hope to replicate
the concavo-convex surface using 3D-printing technology for the purpose of filling the
unnecessary cavities, and we will take effect beginning with measuring the output of the
current commercial-release cartilage-conduction devices.
5. Conclusions
We embedded pinna simulators with three different hardness levels into the HATS
and compared the outputs with those of human ears for the purpose of calibrating cartilage-
conduction sounds. The spectral shapes of the simulator outputs more closely approxi-
mated those of human ears in the frequency lower than 5 kHz as the hardness decreased
from A40 to A10. The hardness value of the simulator (A20 or A10) corresponded to that of
when a durometer is pressed onto the ear tragus of a human ear, although anatomically
removed aural cartilage is harder. While an ideal pinna simulator might have a layer
structure that simulates the soft skin and hard aural cartilage of the human ear, a pinna
simulator with a uniform structure is more easily manufactured. The ideal design must
approximate the output of human ears via a careful selection of materials, hardness, and
mass. In addition, we expect that the excessively emphasized SPL in the higher frequency
than 5 kHz will be managed by designing the concavo-convex surface on the base of
the simulators.
Appl. Sci. 2022, 12, 12532 7 of 8
Author Contributions: The conceptualization, methodology, data analysis, and original draft of this
study were developed by R.S., and the discussion and subsequent conclusion were supervised by
H.H. and T.N. All authors have read and agreed to the published version of the manuscript.
Funding: This research was supported by a Grant-in-Aid for Science Research (B) from the Japan
Society for the Promotion of Science (18H03560).
Informed Consent Statement: Not applicable.
Data Availability Statement: Not applicable.
Acknowledgments: The authors thank Masaki Kawashima (Exseal, Co., Ltd.) for making the pinna
simulators. We thank R.W. Haase and Sydney Koke, from the Edanz Group (https://en-author-
services.edanzgroup.com/, accessed on 9 November 2022) for editing a draft of this manuscript. We
also thank the Elsevier Permission Granting Team for permitting us to reprint the figure.
Conflicts of Interest: The authors declare no conflict of interest.
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