Abstract
Our mental representations of our body are continuously updated through multisensory bodily feedback as we move and interact with our environment. Although it is often assumed that these internal models of body-representation are used to successfully act upon the environment, only a few studies have actually looked at how body-representation changes influence goal-directed actions, and none have looked at this in relation to body-representation changes induced by sound. The present work examines this question for the first time. Participants reached for a target object before and after adaptation periods during which the sounds produced by their hand tapping a surface were spatially manipulated to induce a representation of an elongated arm. After adaptation, participants’ reaching movements were performed in a way consistent with having a longer arm, in that their reaching velocities were reduced. These kinematic changes suggest auditory-driven recalibration of the somatosensory representation of the arm morphology. These results provide support to the hypothesis that one’s represented body size is used as a perceptual ruler to measure objects’ distances and to accordingly guide bodily actions.
Introduction
In our everyday interaction with the environment, most of us perform many physical actions that allow our body to reach, grab or point at different objects. For most of us these actions seem to occur smoothly, mostly automatically. This successful and smooth interaction with the environment is enabled by the use of internal models of body shape and posture (; ). To account for changes in body configuration or structural changes that occur when the body moves or ages, these body models are continuously updated (). Neuroscience and psychological research have repeatedly shown that updates in the internally represented body models, the so-called body-representations, occur in response to the continuous multisensory input we receive on our body (). For instance, experiments on the “rubber-hand illusion” (RHI) demonstrated that a rubber arm can be incorporated into one’s body model, if one observes touches to the rubber arm while synchronously feeling touch delivered to their own, unseen, arm (). This illusion results from the integration of congruent sensory information received through vision and touch. Other studies have shown that feelings of ownership over a rubber hand can be also elicited during active-touch conditions, in which one delivers touch to the seen fake hand and in synchrony receives touch to one’s own unseen hand (), and by synchronous seen and felt movement of a hand and one’s own unseen hand (; ; ; ), thus highlighting the influence of proprioceptive cues in this illusion.
Similarly, previous studies have shown that wielding a tool that serves to act with one’s arm upon relatively distant objects, in other words, a tool that physically extends the arm, yields an extension of the represented arm length (, ; ). In this case, extension of the represented arm length also derives from the integration of congruent sensory information, as visual events at the tip of the tool are contingent with tactile information received at the hand (). At the same time, updates in body-representation can occur without the involvement of vision. For instance, some studies have shown that vibrations delivered to one’s bicep tendon or wrist may induce the illusory feeling of one’s arm extending thus altering the perceived position of one’s hand in space. When this hand is touching another body part (e.g., a finger of the other hand, one’s waist) one may experience distortions in the represented shape or size of this other body part (; ; ).
More recently it has also been demonstrated that updates on body-representation can occur through audition, thus providing evidence of the supramodal nature of body-representation ( for a review). For instance, altering the sound of the impact of an object on one’s hand modifies the felt material of one’s own hand (). Apart from these effects of sound in perceived body material properties, in a previous study we showed that altering action related sounds can elicit changes in the represented body dimensions. In particular, we showed that altering the perceived position of the sounds produced by one’s hand when tapping on a surface recalibrates the represented length of one’s arm (). These changes in represented length of one’s arm were evidenced by changes in perceived tactile distances on the arm (a measure also used by ; ; ,; ). A subsequent study showed that the observed changes in perceived tactile distance correlated with feelings of one’s arm having elongated ().
Because the representation of an action engages a mental representation of the general body structure that allows this action to be produced (; ), it is often assumed that the changes in body-representation evoked by multisensory bodily inputs will have implications in the way actions are performed. However, only a few studies have actually looked at the effects of these body-representation changes on movement or goal directed actions. Among these studies are those reporting that the RHI influences subsequent grasping responses, as a consequence of the grip aperture of the rubber hand () or the visual size of the rubber hand (; see also related effects on perceived weight of objects reported by ), or the studies showing that the RHI influences subsequent reaching movements, as a consequence of the shift in the perceived hand position (; ), although note that failed to find such an influence on reaching movements. The majority of studies have rather looked at changes in bodily feelings, perceived position of the body in space or perceived tactile distances, as reviewed above. Some of these changes might be linked to updates in internal models that are aimed to facilitate successful and smooth interactions with the environment. For instance, changes in tactile distance perception suggest recalibration of somatosensory receptive fields (), and the control of body movements is known to rely on the somatosensory representation of the body morphology (; ). Indeed, showed that using a 40 cm-long mechanical grabber resulted both in shifts in tactile localization and in alterations in the kinematics of subsequent reaching movements performed without the tool: these movements changed in a way consistent with reaching movements performed with a ‘longer’ arm. However, given that multiple body-representations coexist in the human brain and that their plasticity is a task dependent process (), the question of whether action sounds can evoke changes in the internal models of arm morphology involved in facilitating action remains open.
In the present study we investigated the potential effect of action sounds on subsequent goal directed actions. In particular, we took measures of arm kinematics before and after exposure to the audio-tactile adaptation phase used in our previous studies to induce alterations in the represented arm length (, ). We adopted the reaching task from ) study in which the reaching movements after a period of tool-use were characterized by longer latencies and reduced amplitudes in velocity and acceleration movement parameters. As the authors showed in an additional experiment, these changes in kinematics are consistent with reaching movements performed with a ‘longer’ arm, as the very same kinematic differences were found when comparing free-hand grasping movements of individuals with a longer arm with those movements performed by individuals with a shorter arm. By looking at whether people behave as if their arm was longer, we aim to provide a measure of implicit changes in the represented arm that relates to goal directed actions.
Materials and Methods
Participants
Eighteen participants (Mage ±SD = 22.61 ± 4.1 years; age range from 18 to 32 years; nine females and nine males) took part in the experiment. All participants reported having normal hearing and normal tactile perception, and were naïve as to the purposes of the study. Behavioral data from one of the conditions for two participants were lost due to recording problems, and therefore, all data from these two participants were excluded from the analyses, which were performed on the remaining sixteen participants (Mage ±SD = 23 ± 4.2 years; age range from 18 to 32 years; eight females and eight males). Arm length was not taken into account when recruiting participants but there was a reasonable variation in arm length across participants (M = 71.69 cm, SD = 6.02 cm, range 63–81 cm). Participants were paid for their time and gave their informed written consent prior to their inclusion in the studies. The experiment was conducted in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and approved by the ethics committee of University College London.
Apparatus and Materials
The apparatus and materials used for the audio-tactile “tapping” task (see the next section) were identical to those used in . A schema of the experimental set-up is displayed in Figure 1. Participants were seated in a chair, blindfolded and wearing a pair of closed headphones with very high passive ambient noise attenuation (Sennheiser HDA 200). A table was placed to the right of the participants. The height between the participants’ right ear and the surface of the table was approximately 40 cm. A pair of light-emitting diodes (LEDs) of different colors was positioned in front of the participants, at eye level and a distance of 50 cm. They were bright enough so that participants could see the light through the blindfold. The ‘fixation’ LED served as the center fixation point, and the ‘task’ LED was used by participants to perform the experimental task, as described in the next section. During the experimental sessions participants were instructed to refrain from turning their head sideways from the fixation point.
FIGURE 1
In Figure 1, one can see an array of six “tapping-positions” (marked in black color), and an array of six simulated “source locations” (marked in gray color), which replicate those used in our previous study (
A piezoelectric transducer (Schaller Oyster 723 Piezo Transducer Pickup), attached to the table, was used to detect the participants’ taps and trigger the auditory stimulation. In the Synchronous condition, the auditory stimulus was triggered in synchrony with the participant’s tap on the table. To note, the latency of the signal-processing module was in total less than 4 ms. Such short latency is unperceivable across sensory modalities, as it falls well within the intersensory temporal synchrony window (
The actual sound of the participants’ taps on the table was attenuated by the high ambient-noise attenuation headphones, and masked by adding a low level of background noise (interaural uncorrelated pink noise, 20–13000 Hz) to the headphone signals throughout the entire duration of the audio-tactile .. tapping .. task (see Procedure section).
The apparatus used for the kinematic recordings consisted of four reflective markers placed on the participant’s right arm. The first marker was placed on the dorsum of the distal phalanx of the index finger; the second marker was placed on the styloid process of the radius at the level of the wrist; the third marker was placed on the elbow joint on the outer side; and the fourth marker was placed on the shoulder joint on the scapular acromion. An additional marker constituted the target object. The spatial position of the markers was recorded with an optical motion capture system (Vicon V-series comprising six infrared cameras) with a sampling rate of 100 Hz and less than 3 mm 3D resolution at an applied distance of approximately 5 m. In this experiment the 3D resolution was even higher than 3 mm since the applied distance was smaller than 2 m.
Tasks
Reaching Task
At the beginning of the experimental session, blindfolded participants were instructed to search for a target object with their hand and to touch it so to memorize its location (
Note that when performing this reaching task, since participants were blindfolded, they were not always correct in reaching the target when completing their movement. If participants failed to reach the target during a reaching trial, they were subsequently asked to search for the target by means of tactile exploration, so that they confirmed its location before the start of next adaptation phase (as in
The reaching task was repeated twelve times before the first audio-tactile tapping task (Pre-test) and then once more after each audio-tactile tapping task (Post-test). Pre-test served as a baseline measure to which to refer the post-test values (post-adaptation measure). The instructions and task were identical for the Pre-test and the Post-test in all respects, including the instruction to perform a tactile exploration until reaching the target, before moving on to the next adaptation phase, in case of failure in reaching it during the first attempt.
Audio-Tactile “Tapping” Task (Adaptation Task)
As displayed in Figure 1, participants were required to look straight to the ‘fixation’ LED and to perform the simple action of tapping on the table using their right hand, while keeping their palm open and their arm ventral side down [see
After 10 taps, a signal (‘task’ LED) indicated to the participants to extend their arm rightward by 10 cm, and tap again 10 times at the new tapping-position (farther from their body), with the auditory stimulus presented from the subsequent source location in the array (i.e., at double the distance to the tapping-position). This procedure was repeated for all six tapping positions, making a total of 60 taps on the table and ending with the farthest away tapping position and simulated source location. The Asynchronous condition served as the control condition as asynchrony disrupts the feelings of agency over the tapping sounds and these feelings are necessary in order for auditory inputs to change body-representation (
After completion of the 60 taps conforming the tapping task participants were instructed to move their arm back to the initial starting position and wait for a go-signal to perform the reaching task.
Procedure
At the start of the experimental session, the participant’s arm length was measured from the right acromion (shoulder joint) to the middle finger-tip in order to check for possible individual differences in arm kinematics due to arm length (see
Next, participants completed two experimental sessions, each containing two stages: (1) 12 repeats of the pre-stimulation reaching task (Pre-test), (2) 12 repeats of an experimental trial in which participants first performed the audio-tactile tapping task (60 taps, 10 taps in each tapping-position) and immediately after this adaptation phase they performed a post-stimulation reaching task (Post-test). Participants were blindfolded throughout the experimental session. The experimental sessions differed in the auditory condition (Synchronous or Asynchronous) during the audio-tactile tapping task. Each experimental session (Synchronous or Asynchronous) lasted on average for 20 min. The order of their presentation was randomized.
At the end of each session (Synchronous or Asynchronous), the subjective experience of participants during the audio-tactile tapping task was assessed with a questionnaire containing eight statements, adopted from our previous studies (
Data Analyses
The data analyses followed the procedure described in
Behavioral trials were excluded from the analyses if the value of any of the parameters extracted for that trial shifted by more than two standard deviations from the overall mean for that given parameter. In total 1.7% of the trials were excluded from the analyses. As already mentioned, the trials in which participants failed to reach the target were not excluded from the analysis as they were important to calculate the effect over the average reached distances, which served as a measure of recalibration of the length of the represented arm. For all statistical tests, the alpha level was set at 5%.
Results
Reaching Task
The mean values ± SE for all measures are presented in Table 1. Initial analyses did not show any difference in the Pre-test values for any of the measures across Synchronous and Asynchronous conditions (p > 0.25), thus confirming the validity of these values as baseline.
Table 1
| Measure | Synchronous | Asynchronous | ||
|---|---|---|---|---|
| Pre-test | Post-test | Pre-test | Post-test | |
| Mean velocity | 810.63 (88.78) | 713.68 (86.39) | 785.32 (78.33) | 741.42 (91.65) |
| Peak velocity | 1625.68 (177.52) | 1464.41 (179.81) | 1578.58 (150.78) | 1515.66 (186.66) |
| Peak acceleration | 231.14 (53.47) | 207.94 (47.40) | 221.02 (42.46) | 233.29 (57.20) |
| Latency peak velocity | 204.86 (14.78) | 227.43 (21.39) | 204.28 (13.57) | 216.16 (17.66) |
| Latency peak acceleration | 50.99 (7.70) | 61.35 (12.64) | 47.87 (4.54) | 51.05 (5.72) |
| Reached position | 445.47 (3.49) | 432.44 (3.47) | 444.77 (3.27) | 436.63 (4.33) |
| Movement time | 595.23 (53.46) | 693.57 (74.06) | 647.51 (54.46) | 717.39 (68.69) |
Results from the reaching task (N = 16).
Mean velocity (mm/s), mean latency (ms) and amplitude of the peak velocity (mm/s) and acceleration (mm/s2) of the reaching movements, and mean reached position (in mm) and movement time (in ms) for each experimental condition and for both the Pre- and Post-test (all ±SEM).
As in
Table 2
| Synchronous | Asynchronous | ||||
|---|---|---|---|---|---|
| Pre-test | Post-test | Pre-test | Post-test | ||
| Mean velocity | ‘Short arm’ group | 796.72 (105.90) | 765.78 (109.80) | 805.00 (97.39) | 798.29 (118.61) |
| ‘Long arm’ group | 824.54 (150.03) | 661.58 (138.39) | 765.63 (129.22) | 684.54 (144.93) | |
| Peak velocity | ‘Short arm’ group | 1613.50 (185.88) | 1523.54 (172.03) | 1637.63 (193.16) | 1643.98 (223.92) |
| ‘Long arm’ group | 1637.85 (316.95) | 1405.29 (328.58) | 1519.54 (243.17) | 1387.34 (307.37) | |
| Peak acceleration | ‘Short arm’ group | 201.95 (35.79) | 211.95 (49.76) | 229.60 (53.30) | 245.55 (77.90) |
| ‘Long arm’ group | 260.33 (103.58) | 203.94 (84.57) | 212.45 (69.77) | 221.03 (88.94) | |
| Latency peak velocity | ‘Short arm’ group | 198.64 (14.24) | 217.89 (32.97) | 192.48 (22.74) | 204.16 (26.92) |
| ‘Long arm’ group | 211.08 (26.89) | 236.97 (29.13) | 216.07 (15.23) | 228.16 (23.90) | |
| Latency peak acceleration | ‘Short arm’ group | 56.11 (12.35) | 59.13 (16.24) | 52.21 (6.78) | 50.63 (6.15) |
| ‘Long arm’ group | 45.8 (9.70) | 63.5 (20.49) | 43.54 (6.09) | 51.47 (10.13) | |
| Reached position | ‘Short arm’ group | 444.54 (4.63) | 437.93 (5.10) | 446.38 (5.70) | 445.24 (5.45) |
| ‘Long arm’ group | 446.40 (5.52) | 426.96 (4.12) | 443.15 (3.56) | 428.02 (5.44) | |
| Movement time | ‘Short arm’ group | 557.94 (81.43) | 580.91 (98.87) | 614.51 (71.23) | 666.20 (101.01) |
| ‘Long arm’ group | 632.52 (72.25) | 806.24 (100.53) | 680.52 (85.60) | 768.57 (96.30) | |
Results from the reaching task split according to participants’ arm length (‘short arm’ and ‘long arm’ groups, N = 8 in each group).
Mean velocity (mm/s), mean latency (ms) and amplitude of the peak velocity (mm/s) and acceleration (mm/s2) of the reaching movements, and mean reached position (in mm) for each experimental condition and for both the Pre- and Post-test (all ±SEM).
Our main analysis focused on the effect of audio-tactile stimulation across Synchronous and Asynchronous conditions. For all variables we conducted Analyses of Variance (ANOVAs) with 2 × 2 within-subjects factors, ‘audio-tactile synchronicity’ (Synchronous and Asynchronous) and ‘time of test’ (Pre-test and Post-test), and the between-subjects factor ‘arm length group’ (long arm and short arm). We tested whether the distributions of the residual errors of the ANOVAs were normally distributed using the Shapiro–Wilk test. Only the residual errors related to the latency of the peak velocity (all ps > 0.194), the mean reached position (all ps > 0.233) and the movement time (all ps > 0.181) passed the normality test. Nevertheless, Q–Q plots for the residual errors of the variables mean velocity, peak velocity, peak acceleration, and latency of the peak acceleration showed moderate deviations from normality. Given that parametric statistical tests (ANOVAs) are quite robust to moderate deviations from normality (e.g.,
For the mean reached positions, the main effect of ‘time of test’ [F(1,15) = 4.8; p = 0.045] was significant, while the effect of ‘audio-tactile synchronicity’ (p > 0.250) and the double interaction (p = 0.190) were not significant. Overall there was a significant decrease in the reached position from Pre- to Post-test, as displayed in Figure 2C, but this decrease did not significantly interact with the effect of audio-tactile synchronicity. There were no significant interactions between ‘arm length group’ and the within-subjects factors. Results split according to participants’ arm length are displayed in Table 2 and Figure 3C.
FIGURE 2

Results from the reaching task.(A) Mean velocity and (B) peak velocity of the index finger during the reaching movement, (C) mean reached position and (D) mean movement time, in pre- and post-test measures for each of the two experimental sessions (Synchronous and Asynchronous). Error bars indicate the SEM. ∗Denotes significant differences between conditions. In addition, the double interaction between ‘time of test’ and ‘audio-tactile synchronicity’ was significant both for the mean velocity and the peak velocity data.
FIGURE 3

Results from the reaching task split according to participants’ arm length (‘short arm’ and ‘long arm’ groups, N = 8 in each group).(A) Mean velocity and (B) peak velocity of the index finger during the reaching movement, (C) mean reached position and (D) mean movement time, in pre- and post-test measures for each of the two experimental sessions (Synchronous and Asynchronous). Error bars indicate the SEM. ∗Denotes significant differences between conditions. In addition, the double interaction ‘time of test’ and ‘arm length group’ was significant for the mean velocity and the triple interaction between ‘time of test,’ ‘audio-tactile synchronicity’ and ‘arm length group’ was significant for the movement time.
For the mean velocity, the main effect of ‘time of test’ [F(1,14) = 11.54; p = 0.004] was significant, as well as its interaction with ‘audio-tactile synchronicity’ [F(1,14) = 5.36; p = 0.036], while the main effect of ‘audio-tactile synchronicity’ was not significant (p > 0.250). A significant decrease in the mean velocity from Pre- to Post-test was observed for the Synchronous condition [t(15) = 3.59, p = 0.003], but not for the Asynchronous condition (p = 0.118), as displayed in Figure 2A. Further, there was an interaction between ‘time of test’ and ‘arm length group’ [F(1,14) = 6.2; p = 0.026], due to a larger decrease in mean velocity from Pre- to Post-test for the ‘long arm’ but not for the ‘short arm’ group. This decrease reached significance only for the ‘long arm’ group [t(7) = 4.29, p = 0.004]. An inspection of the results summarized in Table 2 and Figure 3A suggested larger Pre-Post differences in mean velocity in the critical (Synchronous) than in the control (Asynchronous) condition for the ‘long arm’ group than for the ‘short arm’ group (‘Long arm’ group: Mean Synchronous Pre-Post velocity change = -162.96 mm/s, SE = 32.07; Mean Asynchronous Pre-Post velocity change = -81.09 mm/s, SE = 33.24; ‘Short arm’ group: Mean Synchronous Pre-Post velocity change = -30.94 mm/s, SE = 29.08; Mean Asynchronous Pre-Post velocity change = -6.71 mm/s, SE = 38.84); however, the triple interaction between ‘time of test,’ ‘audio-tactile synchronicity’ and ‘arm length group’ did not reach significance (p > 0.23). These results suggest that the observed baseline shifts from Pre- to Post-test interacted with arm length and that this interaction was independent of ‘audio-tactile synchronicity.’
For the peak velocity, the main effect of ‘time of test’ [F(1,15) = 5.80; p = 0.029] was significant, as well as its interaction with ‘audio-tactile synchronicity’ [F(1,15) = 5.17; p = 0.038], while the main effect of ‘audio-tactile synchronicity’ was not significant (p > 0.250). A significant decrease in the peak velocity from Pre- to Post-test was observed for the Synchronous condition [t(15) = 3.34, p = 0.004], but not for the Asynchronous condition (p = 0.264), as displayed in Figure 2B. There were no significant interactions between ‘arm length group’ and the within-subjects factors (see Table 2; Figure 3B). Thus, our hypothesis that the auditory-induced illusory effect induced in the Synchronous condition modifies the kinematic of subsequent reaching movements was confirmed, providing evidence of changes in the represented arm length. For the peak acceleration, and the latencies, no significant effects, interactions or comparisons were found.
For the movement time (from movement onset to movement end), the main effect of ‘time of test’ [F(1,14) = 12.58; p = 0.003] was significant, while the main effect of ‘audio-tactile synchronicity’ or the interaction between both factors were not significant (both p > 0.21). A significant increase in the movement time was observed from Pre- to Post-test, as displayed in Figure 2D. Further, there was a triple interaction between ‘time of test’, ‘audio-tactile synchronicity’ and ‘arm length group’ [F(1,14) = 6.92; p = 0.020], due to a larger Pre-Post increase in movement time in the critical (Synchronous) condition for the ‘long arm’ group than for the ‘short arm’ group [F(15) = 10.91, p = 0.005], which was not observed for the control (Asynchronous) condition (p > 0.250; see Figure 3D). This decrease reached significance only for the ‘long arm’ group [t(7) = 4.84, p = 0.002]. These results suggest longer movement times from Pre- to Post-test; these baseline shifts interacted with arm length in the Synchronous condition, with longer movement times from Pre- to Post-test for the ‘long arm’ group.
Note that additional ANCOVA tests with 2 × 2 within-subjects factors, ‘audio-tactile synchronicity’ and ‘time of test’ (Pre-test and Post-test), and ‘arm length’ as a covariate, revealed a similar interaction on velocity data between ‘time of test’ and ‘arm length’ as the one reported for the mean velocity data analysis when ‘arm length group’ was treated as a between-subjects factors. The ANCOVAs showed a significant interaction between ‘time of test’ and ‘arm length’ for the mean velocity [F(1,14) = 15.12; p = 0.002] and for the peak velocity [F(1,14) = 9.45; p = 0.008], and a near significance interaction between ‘time of test’ and ‘arm length’ for the mean reached positions [F(1,14) = 4.10; p = 0.062]. For the peak acceleration, movement time, and latency data, no interactions were found.
Questionnaire
The full set of statements and mean responses (±SEM) are presented in Figure 4. In order to investigate the effect of audio-tactile stimulation on the subjective experience of participants across the conditions, we used non-parametrical Wilcoxon Signed Ranks Tests to analyze the data. We observed significant differences between the two conditions for the first two statements. Firstly, while participants in the Synchronous audio-tactile condition felt that they caused the sound, they did not feel the same for the Asynchronous condition (z = 3.21, p = 0.001). Secondly, we also found that while participants in the Synchronous condition felt that the sound came from the same location where the hand was, they did not feel this happened in the Asynchronous condition (z = 2.64, p = 0.008). The disruption of feelings of being the agent of the sounds and of sound and hand being at the same location during the Asynchronous condition matches the results from previous studies and provides support to our choice of the Asynchronous condition as a control condition. Feelings of agency and of spatio-temporal congruency between action and sensory effect are necessary in order for auditory inputs to change body-representation (
FIGURE 4

Mean level of agreement for each questionnaire statement across Synchronous and Asynchronous conditions. Error bars indicate the SEM. ∗Denotes significant differences between conditions as a result of the auditory manipulation.
Then, given that the kinematics data revealed larger baseline shifts for the ‘long arm’ group in the Synchronous condition, which suggested larger illusory effects for this group, we also verified if the subjective experience of participants could be affected by arm length. We checked for possible individual differences in feelings elicited during the audio-tactile adaptation due to arm length. Based on the kinematic results, we hypothesized that, in the Synchronous condition, participants with longer arms would agree more with the statements related to a feeling of arm elongation, and potentially also with those statements related to a blurring of the perceived length of the arm or hand position. In order to investigate this hypothesis we conducted one-tailed Spearman’s rho correlations between the participant’s arm length and the self-reported level of agreement for all statements in the Synchronous and Asynchronous conditions. For the Synchronous condition we found that participants with longer arms agreed more with the statement “my arm felt longer than usual” [rS(16) = 0.45, p = 0.041] and “I couldn’t really tell where my hand was” [rS(16) = 0.47, p = 0.033]. All other correlations were far from the significance level.
Correlations between Implicit and Explicit Measures
In order to investigate how the observed changes in our objective measures related to participants’ subjective experience, we performed correlation analyses between behavioral and subjective data. In particular, we conducted two-tailed Spearman’s rho correlations between the change from Pre- to Post-test in all kinematic parameters listed in Table 1 in the Synchronous and Asynchronous conditions and the self-reported level of agreement for all statements in these conditions.
Results showed that, for the Synchronous condition, increases in mean reached position correlated significantly with increases in level of agreement with the statement “It seemed like the sound I heard was caused by me” [rS(16) = 0.52, p = 0.040], while decreases in mean and peak velocity correlated significantly with increases in level of agreement, respectively, with the statements “my own arm was out of my control” [rS(16) = -0.54, p = 0.03] and “I couldn’t really tell where my hand was” [rS(16) = -0.57, p = 0.022]. In addition, we observed that increases in the latency of the peak velocity correlated significantly with increases in level of agreement with the statement “my arm felt longer than usual” [rS(16) = 0.50, p = 0.047]. We also observed a near significant correlation between increases in movement time and the level of agreement with the statement “my arm felt longer than usual” [rS(16) = 0.49, p = 0.054].
We also found significant correlations between implicit and explicit measures for the Asynchronous condition, which proves agreement between measures. In this case, decreases in mean velocity and increases in movement time correlated significantly with increases in level of agreement with the statement “my arm felt longer than usual” [mean velocity: rS(16) = -0.50, p = 0.049; movement time: rS(16) = 0.56, p = 0.024] and that decreases in peak velocity correlated significantly with increases in level of agreement with the statement “I couldn’t really tell where my hand was” [rS(16) = -0.53, p = 0.036]; it should be noted, however, that participants overall disagreed more with these statements and that the behavioral measures indicated a smaller recalibration of represented arm in the Asynchronous condition than in the Synchronous condition. In addition, we observed that increases in the latency of the peak velocity correlated significantly with increases in level of agreement with the statements “I couldn’t really tell where my hand was” [rS(16) = 0.52, p = 0.038] and “the experience of my arm was less vivid than normal” [rS(16) = 0.54, p = 0.030].
Discussion
The results from this study show that the manipulation of the spatial position of the sounds produced by one’s hand has an effect on the kinematics of goal directed arm actions. Importantly, this finding provides the first evidence of an auditory-driven recalibration of the internal models of body morphology that are possibly aimed at facilitating interactions with the environment. We show changes in the kinematics of reaching movements after periods of audio-tactile adaptation in which participants were exposed to spatially manipulated versions of the sounds generated by the tapping of their hand on a surface. These kinematic changes were characterized by reduced mean and peak amplitudes in the velocity of the reaching movements, and by longer movement times. Remarkably, these changes correspond with the kinematic profile of arm reaching movements performed by participants with longer arms [see
Recalibration of the Internal Models of Arm Morphology Engaged in Action
We previously observed that exposure to the above-mentioned audio-tactile adaptation when tapping a surface with the hand may result in feelings of arm elongation and that it also changes the perception of tactile distances for objects in contact with the arm (
Previous experiments have reported that a general recalibration from Pre- to Post-test due to exposure to multisensory adaptation often occurs (e.g.,
Alterations in arm kinematics as a result of changes in the somatosensory representation of arm morphology induced by action sounds may be interpreted in the context of ‘forward internal models’ of motor-to-sensory transformations (
Taken together with our current results these findings suggest that action sounds contribute to the formation of body-representation and to guide bodily movements. It should be considered that these sounds are omnipresent since the auditory system provides a continuous stream of information (because our ears are not “turned off” in the same way that we regularly block vision by closing our eyes or by turning our head).
Subjective Experiences in Response to the Manipulated Action Sounds
The results from the questionnaire replicated our previous findings that asynchrony between tapping action and sound disrupts the feelings of agency over the tapping sounds and of one’s hand being at the same location as the sounds (
Nevertheless, in one of our previous studies using the same setup and paradigm described in the current study, we found a correlation between implicit (i.e., perceived tactile distance) and explicit measures of elongation in the represented arm (
Note that while we found that increases in mean reached position correlated significantly with increases in level of agreement with the statement “It seemed like the sound I heard was caused by me,” this positive correlation does not go against our hypothesis that a longer represented arm would lead to reach toward a more proximal location. Overall, feelings of agency in the Synchronous condition were always high, as reflected by the strong level of agreement with the statement “I felt the sound I heard was caused by me,” and there was an overall tendency to decrease the reached position from pre- to post-test. A tentative explanation for this correlation could be that, while agency is necessary to create the illusion, then this illusion may lead to surprise when reaching to the target (for instance, due to an unexpected delay in touching the table or to not having reached the target at all) and to an overall blurriness of the feelings related to one’s hand as captured in the self-reports collected after the experience. This blurring over one’s body was also reflected in the negative correlations found between another measure that we took as a proxy of the illusion of elongation in the represented arm (i.e., reduction in reaching velocity) and participants’ explicit reports of one’s arm being out of control and not knowing where one’s hand was. It is thus plausible that this blurring and loss of agency over one’s body and the sounds it produces are part of the process of updating body-representation, and it may be also possible that these feelings change during the time passed from the audio-tactile task and the subsequent reaching task to the moment when self-report is captured, and this is something that future research should clarify. Nevertheless, we can see that during the Synchronous condition participants strongly agreed with the statement “I felt the sound I heard was caused by me,” as already mentioned, and they also disagreed with the statements “my own arm was out of my control” and “I couldn’t really tell where my hand was.”
Auditory-Induced Illusory Effects in Relation to the Actual Arm Length
We previously had found that the illusory effects on represented arm length when manipulating auditory sources depended on the distance to these sources (
The “near space” is the region of space immediately surrounding the body, which in the field of cognitive neurosciences is sometimes also referred as “peripersonal space” (
While our study was not designed to test the hypothesis that auditory-induced illusory effects would be maximized when auditory sources are located in the “near space,” the recorded arm length allowed us to look at our results also in relation to this hypothesis. In particular, we hypothesized that the illusion would be larger for those people with longer arms as more sound sources would fall inside their near space and contribute to the illusion. The behavioral results were in support of this hypothesis: larger kinematics changes from the control Asynchronous to the Synchronous condition were observed for the ‘long arm’ group than for the ‘short arm’ group. The comparison between groups reached significance for the movement time parameter. This result suggests that people with longer arm experienced a larger illusion of arm elongation, as it is consistent with the reports of
Conclusion
The results presented in this study show that inducing in people a representation of an elongated arm, by altering the spatial position of the sounds generated by tapping their hand on a surface, makes them perform reaching movements in a way consistent with having a longer arm. These results provide the first evidence that body-representation changes induced by sound influence the kinematics of goal-directed actions. They provide further support to the hypothesis that the represented size of the body is used to calibrate the perceived distances to objects and to guide bodily actions. Further explorations may provide an insight on whether body-representation changes induced by sound are more easily induced when sound sources are located in the “near space” and on whether illusions of body shrinkage can be induced via sound.
Statements
Author contributions
All authors contributed to the conception and design of the work, interpretation of data and revision of the drafts of the work. AT-J acquired and analyzed the data, and drafted the work. All authors agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved, and approved this final version of the manuscript.
Funding
AT-J was supported by the ESRC grant ES/K001477/1 (“The hearing body”) and by the MINECO Ramón y Cajal research contract RYC-2014-15421.
Acknowledgments
The authors are grateful to Wallizada Mohibullah for his help on data extraction.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
AbekawaN.GomiH. (2010). Spatial coincidence of intentional actions modulates an implicit visuomotor control.J. Neurophysiol.1032717–2727. 10.1152/jn.91133.2008
2
Aimola DaviesA. M.WhiteR. C.ThewG.AimolaN. M.DaviesM. (2010). Visual capture of action, experience of ownership, and the illusion of self-touch: a new rubber hand paradigm.Perception39830–838. 10.1068/p6610
3
AzañónE.TamèL.MaravitaA.LinkenaugerS. A.FerrèE. R.Tajadura-JiménezA.et al (2016). Multimodal contributions to body representation.Multisens. Res.29635–661. 10.1163/22134808-00002531
4
BanakouD.GrotenR.SlaterM. (2013). Illusory ownership of a virtual child body causes overestimation of object sizes and implicit attitude changes.Proc. Natl. Acad. Sci. U.S.A.11012846–12851. 10.1073/pnas.1306779110
5
BlakemoreS.-J.WolpertD. M.FrithC. D. (2002). Abnormalities in the awareness of action.Trends Cogn. Sci.6237–242. 10.1016/S1364-6613(02)01907-1
6
BotvinickM.CohenJ. (1998). Rubber hands ‘feel’ touch that eyes see.Nature391:756. 10.1038/35784
7
CanzoneriE.MarzollaM.AmoresanoA.VerniG.SerinoA. (2013a). Amputation and prosthesis implantation shape body and peripersonal space representations.Sci. Rep.3:2844. 10.1038/srep02844
8
CanzoneriE.UbaldiS.RastelliV.FinisguerraA.BassolinoM.SerinoA. (2013b). Tool-use reshapes the boundaries of body and peripersonal space representations.Exp. Brain Res.22825–42. 10.1007/s00221-013-3532-2
9
CardinaliL.FrassinettiF.BrozzoliC.UrquizarC.RoyA. C.FarneA. (2009). Tool-use induces morphological updating of the body schema.Curr. Biol.19R478–R479. 10.1016/j.cub.2009.05.009
10
CardinaliL.JacobsS.BrozzoliC.FrassinettiF.RoyA. C.FarneA. (2012). Grab an object with a tool and change your body: tool-use-dependent changes of body representation for action.Exp. Brain Res.218259–271. 10.1007/s00221-012-3028-5
11
CulhamJ. C.Cavina-PratesiC.SinghalA. (2006). The role of parietal cortex in visuomotor control: what have we learned from neuroimaging?Neuropsychologia442668–2684. 10.1016/j.neuropsychologia.2005.11.003
12
de VignemontF.EhrssonH. H.HaggardP. (2005). Bodily illusions modulate tactile perception.Curr. Biol.151286–1290. 10.1016/j.cub.2005.06.067
13
EhrssonH. H.KitoT.SadatoN.PassinghamR. E.NaitoE. (2005). Neural substrate of body size: illusory feeling of shrinking of the waist.PLoS Biol.3:e412. 10.1371/journal.pbio.0030412
14
ErnstM. O.BülthoffH. H. (2004). Merging the senses into a robust percept.Trends Cogn. Sci.8162–169. 10.1016/j.tics.2004.02.002
15
FarnèA.LàdavasE. (2002). Auditory peripersonal space in humans.J. Cogn. Neurosci.141030–1043. 10.1162/089892902320474481
16
FujisakiW.ShimojoS.KashinoM.NishidaS. Y. (2004). Recalibration of audiovisual simultaneity.Nat. Neurosci.7773–778. 10.1038/nn1268
17
GrazianoM. S. A.GrossC. G. (1998). Spatial maps for the control of movement.Curr. Opin. Neurobiol.8195–201. 10.1016/S0959-4388(98)80140-2
18
GrazianoM. S. A.ReissL. A. J.GrossC. G. (1999). A neuronal representation of the location of nearby sounds.Nature397428–430. 10.1038/17115
19
HaggardP.ChristakouA.SerinoA. (2007). Viewing the body modulates tactile receptive fields.Exp. Brain Res.180187–193. 10.1007/s00221-007-0971-7
20
HaggardP.JundiS. (2009). Rubber hand illusions and size–weight illusions: self-representation modulates representation of external objects.Perception381796–1803. 10.1068/p6399
21
HeadH.HolmesH. G. (1911–1912). Sensory disturbances from cerebral lesions.Brain34102–254. 10.1093/brain/34.2-3.102
22
HeedT.RöderB. (2012). “The body in a multisensory world,” in The Neural Bases of Multisensory Processes Frontiers in Neuroscience, edsMurrayM. M.WallaceM. T. (Boca Raton, FL: CRC Press), 557–580.
23
HolmesN.SpenceC. (2004). The body schema and the multisensory representation(s) of peripersonal space.Cogn. Process.594–105. 10.1007/s10339-004-0013-3
24
KalckertA.EhrssonH. H. (2012). Moving a rubber hand that feels like your own: a dissociation of ownership and agency.Front. Hum. Neurosci.6:40. 10.3389/fnhum.2012.00040
25
KammersM. P.KootkerJ. A.HogendoornH.DijkermanH. C. (2010). How many motoric body representations can we grasp?Exp. Brain Res.202203–212. 10.1007/s00221-009-2124-7
26
KammersM. P. M.de VignemontF.VerhagenL.DijkermanH. C. (2009). The rubber hand illusion in action.Neuropsychologia47204–211. 10.1016/j.neuropsychologia.2008.07.028
27
KeizerA.SmeetsM. A.DijkermanH. C.UzunbajakauS. A.vanElburg APostmaA. (2013). Too fat to fit through the door: first evidence for disturbed body-scaled action in anorexia nervosa during locomotion.PLoS ONE8:e64602. 10.1371/journal.pone.0064602
28
KilteniK.NormandJ. M.Sanchez-VivesM. V.SlaterM. (2012). Extending body space in immersive virtual reality: a very long arm illusion.PLoS ONE7:e40867. 10.1371/journal.pone.0040867
29
KitagawaN.SpenceC. (2006). Audiotactile multisensory interactions in information processing.Jpn. Psychol. Res.48158–173. 10.1111/j.1468-5884.2006.00317.x
30
LacknerJ. R. (1988). Some proprioceptive influences on the perceptual representation of body shape and orientation.Brain111281–297. 10.1093/brain/111.2.281
31
LàdavasE. (2002). Functional and dynamic properties of visual peripersonal space.Trends Cogn. Sci.617–22. 10.1016/S1364-6613(00)01814-3
32
LenggenhagerB.TadiT.MetzingerT.BlankeO. (2007). Video ergo sum: manipulating bodily self-consciousness.Science3171096–1099. 10.1126/science.1143439
33
LewkowiczD. J. (1996). Perception of auditory–visual temporal synchrony in human infants.J Exp. Psychol. Hum. Percept. Perform.221094–1106. 10.1037/0096-1523.22.5.1094
34
LewkowiczD. J. (1999). “The development of temporal and spatial intermodal perception,” inCognitive Contributions to the Perception of Spatial and Temporal Events, edsAscherslebenG.BachmanT.MusselerJ. (Amsterdam: Elsevier), 395–420.
35
LinkenaugerS. A.BülthoffH. H.MohlerB. J. (2015). Virtual arm’s reach influences perceived distances but only after experience reaching.Neuropsychologia70393–401. 10.1016/j.neuropsychologia.2014.10.034
36
LinkenaugerS. A.WittJ. K.ProffittD. R. (2011). Taking a hands-on approach: apparent grasping ability scales the perception of object size.J. Exp. Psychol. Hum. Percept. Perform.371432–1441. 10.1037/a0024248
37
LongoM.HaggardP. (2012). What is it like to have a body?Curr. Dir. Psychol.21140–145. 10.1177/0963721411434982
38
LongoM. R.LourencoS. F. (2007). Space perception and body morphology: extent of near space scales with arm length.Exp. Brain Res.177285–290. 10.1007/s00221-007-0855-x
39
LongoM. R.SerinoA. (2012). Tool use induces complex and flexible plasticity of human body representations.Behav. Brain Sci.35229–230. 10.1017/S0140525X11001907
40
LourencoS. F.LongoM. R.PathmanT. (2011). Near space and its relation to claustrophobic fear.Cognition119448–453. 10.1016/j.cognition.2011.02.009
41
MaisterL.SebanzN.KnoblichG.TsakirisM. (2013). Experiencing ownership over a dark-skinned body reduces implicit racial bias.Cognition128170–178. 10.1016/j.cognition.2013.04.002
42
MaravitaA.IrikiA. (2004). Tools for the body (schema).Trends Cogn. Sci.879–86. 10.1016/j.tics.2003.12.008
43
MarinoB. F.StucchiN.NavaE.HaggardP.MaravitaA. (2010). Distorting the visual size of the hand affects hand pre-shaping during grasping.Exp. Brain Res.202499–505. 10.1007/s00221-009-2143-4
44
McDonaldJ. H. (2014). Handbook of Biological Statistics, 3rd Edn. Baltimore, MD: Sparky House Publishing.
45
MillerL. E.LongoM. R.SayginA. P. (2014). Tool morphology constrains the effects of tool use on body representations.J Exp. Psychol. Hum. Percept. Perform.402143–2153. 10.1037/a0037777
46
NewportR.PearceR.PrestonC. (2010). Fake hands in action: embodiment and control of supernumerary limbs.Exp. Brain Res.204385–395. 10.1007/s00221-009-2104-y
47
Sánchez-VivesM. V.SpanlangB.FrisoliA.BergamascoM.SlaterM. (2010). Virtual hand illusion induced by visuomotor correlations.PLoS ONE5:e10381. 10.1371/journal.pone.0010381
48
SennaI.MaravitaA.BologniniN.PariseC. V. (2014). The marble-hand illusion.PLoS ONE9:e91688. 10.1371/journal.pone.0091688
49
SiriguA.GrafmanJ.BresslerK.SunderlandT. (1991). Multiple representations contribute to body knowledge processing.Brain114629–642. 10.1093/brain/114.1.629
50
Tajadura-JiménezA.BasiaM.DeroyO.FairhustM.MarquardtN.BerthouzeN. (2015a). “As light as your footsteps: altering walking sounds to change perceived body weight, emotional state and gait,” inProceedings of the the CHI Conference on Human Factors in Computing Systems, (Seoul: ACM Press).
51
Tajadura-JiménezA.KitagawaN.ValjamaeA.ZampiniM.MurrayM. M.SpenceC. (2009). Auditory-somatosensory multisensory interactions are spatially modulated by stimulated body surface and acoustic spectra.Neuropsychologia47195–203. 10.1016/j.neuropsychologia.2008.07.025
52
Tajadura-JiménezA.TsakirisM.MarquardtT.Bianchi-BerthouzeN. (2015b). Action sounds update the mental representation of arm dimension: contributions of kinaesthesia and agency.Front. Psychol.6:689. 10.3389/fpsyg.2015.00689
53
Tajadura-JiménezA.VäljamäeA.ToshimaI.KimuraT.TsakirisM.KitagawaN. (2012). Action sounds recalibrate perceived tactile distance.Curr. Biol.22R516–R517. 10.1016/j.cub.2012.04.028
54
Taylor-ClarkeM.JacobsenP.HaggardP. (2004). Keeping the world a constant size: object constancy in human touch.Nat. Neurosci.7219–220. 10.1038/nn1199
55
TsakirisM. (2010). My body in the brain: a neurocognitive model of body-ownership.Neuropsychologia48703–712. 10.1016/j.neuropsychologia.2009.09.034
56
TsakirisM.PrabhuG.HaggardP. (2006). Having a body versus moving your body: how agency structures body-ownership.Conscious. Cogn.15423–432. 10.1016/j.concog.2005.09.004
57
van der HoortB.GuterstamA.EhrssonH. H. (2011). Being barbie: the size of one’s own body determines the perceived size of the world.PLoS ONE6:e20195. 10.1371/journal.pone.0020195
58
VroomenJ.KeetelsM.de GelderB.BertelsonP. (2004). Recalibration of temporal order perception by exposure to audio-visual asynchrony.Cogn. Brain Res.2232–35. 10.1016/j.cogbrainres.2004.07.003
59
WolpertD. M.GhahramaniZ. (2000). Computational principles of movement neuroscience.Nat. Neurosci.31212–1217. 10.1038/81497
60
WolpertD. M.GhahramaniZ.JordanM. I. (1995). An internal model for sensorimotor integration.Science2691880–1882. 10.1126/science.7569931
61
ZopfR.TruongS.FinkbeinerM.FriedmanJ.WilliamsM. A. (2011). Viewing and feeling touch modulates hand position for reaching.Neuropsychologia491287–1293. 10.1016/j.neuropsychologia.2011.02.012
Summary
Keywords
auditory-dependent body-representation, action sounds, body-related sensory inputs, body kinematics, goal directed actions
Citation
Tajadura-Jiménez A, Marquardt T, Swapp D, Kitagawa N and Bianchi-Berthouze N (2016) Action Sounds Modulate Arm Reaching Movements. Front. Psychol. 7:1391. doi: 10.3389/fpsyg.2016.01391
Received
13 June 2016
Accepted
30 August 2016
Published
16 September 2016
Volume
7 - 2016
Edited by
Anna M. Borghi, University of Bologna, Italy
Reviewed by
Konstantina Kilteni, Karolinska Institutet, Sweden; Elisa Canzoneri, École Polytechnique Fédérale de Lausanne, Switzerland
Updates

Check for updates
Copyright
© 2016 Tajadura-Jiménez, Marquardt, Swapp, Kitagawa and Bianchi-Berthouze.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ana Tajadura-Jiménez, atajadura@uloyola.es
This article was submitted to Cognition, a section of the journal Frontiers in Psychology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.