More than skin-deep: integration of skin-based and musculo-skeletal reference frames in localisation of touch

The skin of the forearm is, in one sense, a flat 2D sheet, but in another sense approximately cylindrical, mirroring the 3D volumetric shape of the arm. The role of frames of reference based on the skin as a 2D sheet versus based on the musculo-skeletal structure of the arm remains unclear. When we rotate the forearm from a pronated to a supinated posture, the skin on its surface is displaced. Thus, a marked location will slide with the skin across the underlying flesh, and the touch perceived at this location should follow this displacement if it is localised within a skin-based reference frame. We investigated, however, if the perceived tactile locations were also affected by the rearrangement in underlying musculo-skeletal structure, i.e. displaced medially and laterally on a pronated and supinated forearm, respectively. Participants pointed to perceived touches (Experiment 1), or marked them on a three-dimensional size-matched forearm on a computer screen (Experiment 2). The perceived locations were indeed displaced medially after forearm pronation in both response modalities. This misperception was reduced (Experiment 1), or absent altogether (Experiment 2) in the supinated posture when the actual stimulus grid moved laterally with the displaced skin. The grid was perceptually stretched at medial-lateral axis, and it was displaced distally, which suggest the influence of skin-based factors. Our study extends the tactile localisation literature focused on the skin-based reference frame and on the effects of spatial positions of body parts by implicating the musculo-skeletal factors in localisation of touch on the body

Using Adaptive Psychophysics to Identify the Neural Network Reset Time in Subsecond Interval Timing

State dependent network models of subsecond interval timing propose that duration is encoded in states of neuronal populations that need to reset prior to a novel timing operation in order to maintain optimal timing performance. Previous research has shown that the approximate boundary of this reset interval can be inferred by varying the interstimulus interval between two to-be-timed intervals. However, the estimated boundary of this reset interval is broad (250-500ms) and remains underspecified with implications for the characteristics of state dependent network dynamics subserving interval timing. Here we probed the interval specificity of this reset boundary by manipulating the interstimulus interval between standard and comparison intervals in two subsecond auditory duration discrimination tasks (100 and 200ms) and a control (pitch) discrimination task using adaptive psychophysics. We found that discrimination thresholds improved with the introduction of a 333ms interstimulus interval relative to a 250ms interstimulus interval in both duration discrimination tasks, but not in the control task. This effect corroborates previous findings of a breakpoint in the discrimination performance for subsecond stimulus interval pairs as a function of an incremental interstimulus delay but more precisely localizes the minimal interstimulus delay range. These results suggest that state dependent networks subserving subsecond timing require approximately 250-333ms for the network to reset in order to maintain optimal interval timing

A proxy measure of striatal dopamine predicts individual differences in temporal precision

The perception of time is characterized by pronounced variability across individuals, with implications for a diverse array of psychological functions. The neurocognitive sources of this variability are poorly understood, but accumulating evidence suggests a role for inter-individual differences in striatal dopamine levels. Here we present a pre-registered study that tested the predictions that spontaneous eyeblink rates, which provide a proxy measure of striatal dopamine availability, would be associated with aberrant interval timing (lower temporal precision or overestimation bias). Neurotypical adults (N = 69) underwent resting state eye tracking and completed visual psychophysical interval timing and control tasks. Elevated spontaneous eyeblink rates were associated with poorer temporal precision but not with inter-individual differences in perceived duration or performance on the control task. These results signify a role for striatal dopamine in variability in human time perception and can help explain deficient temporal precision in psychiatric populations characterized by elevated dopamine levels

Reconstructing neural representations of tactile space

Psychophysical experiments have demonstrated large and highly systematic perceptual distortions of tactile space. Such a space can be referred to our experience of the spatial organisation of objects, at representational level, through touch, in analogy with the familiar concept of visual space. We investigated the neural basis of tactile space by analysing activity patterns induced by tactile stimulation of nine points on a 3 × 3 square grid on the hand dorsum using functional magnetic resonance imaging. We used a searchlight approach within pre-defined regions of interests to compute the pairwise Euclidean distances between the activity patterns elicited by tactile stimulation. Then, we used multidimensional scaling to reconstruct tactile space at the neural level and compare it with skin space at the perceptual level. Our reconstructions of the shape of skin space in contralateral primary somatosensory and motor cortices reveal that it is distorted in a way that matches the perceptual shape of skin space. This suggests that early sensorimotor areas critically contribute to the distorted internal representation of tactile space on the hand dorsum

Neural correlates of distorted body representations underlying tactile distance perception

Tactile distance perception is believed to require that immediate afferent signals be referenced to a stored representation of body size and shape (the body model). For this ability, recent studies have reported that the stored body representations involved are highly distorted, at least in the case of the hand, with the hand dorsum represented as wider and squatter than it actually is. Here, we aim to define the neural basis of this phenomenon. In a behavioural experiment participants estimated the distance between touches on two points by adjusting the length of a visually-presented line on the screen. The technique of multidensional scaling (MDS) was used to reconstruct a perceptual map of tactile space. Analysis of spatial distortion using Procrustes alignment showed that maps were stretched in the mediolateral hand axis. In order to determine the neural correlates of these body distortions, we performed an fMRI study. For each participant, we used a searchlight pattern classifier with Euclidean distance on pre-defined regions of interests (ROIs). In order to relate the representations between the different points and to computational models, we compare response-pattern dissimilarity matrices in these ROIs. Similar to the behavioural experiment, we used MDS to reconstruct maps of the neural representation of tactile space using the values from the dissimilarities matrices. We were able to reconstruct the perceptual map of tactile space in the contralateral primary somatosensory and motor cortices. This suggests that these areas are critical to generate the tactile representations of the dorsum of the hand

Seeing the body distorts tactile size perception

Vision of the body modulates somatosensation, even when entirely non-informative about stimulation. For example, seeing the body increases tactile spatial acuity, but reduces acute pain. While previous results demonstrate that vision of the body modulates somatosensory sensitivity, it is unknown whether vision also affects metric properties of touch, and if so how. This study investigated how non-informative vision of the body modulates tactile size perception. We used the mirror box illusion to induce the illusion that participants were directly seeing their stimulated left hand, though they actually saw their reflected right hand. We manipulated whether participants: (a) had the illusion of directly seeing their stimulated left hand, (b) had the illusion of seeing a non-body object at the same location, or (c) looked directly at their non-stimulated right-hand. Participants made verbal estimates of the perceived distance between two tactile stimuli presented simultaneously to the dorsum of the left hand, either 20, 30, or 40 mm apart. Vision of the body significantly reduced the perceived size of touch, compared to vision of the object or of the contralateral hand. In contrast, no apparent changes of perceived hand size were found. These results show that seeing the body distorts tactile size perception

Reconstruction of the neural representations of the tactile space

We examined the neural basis of tactile distance perception by analyzing activity patterns induced by tactile stimulation of nine points on a 3 x 3 square grid on the hand dorsum using functional magnetic resonance (fMRI). We used a searchlight approach within pre-defined regions of interests (ROIs) to compute the pairwise Euclidean distances between the activity patterns elicited by tactile stimulation. Then, we used multidimensional scaling (MDS) to reconstruct skin space at the neural level and compare it with skin space at the perceptual level. Our reconstructions of the shape of skin space in contralateral primary somatosensory (SI) and motor (M1) cortices reveal that it is distorted in a way that matches the perceptual shape of skin space. This suggests that early sensorimotor areas are critical to processing tactile distance perception

Embodying prostheses – how to let the body welcome assistive devices

Comment on “The embodiment of assistive devices—from wheelchair to exoskeleton” by M. Pazzaglia and M. Molinar

Mind the gap: the effects of temporal and spatial separation in localization of dual touches on the hand

In this study, we aimed to relate the findings from two predominantly separate streams of literature, one reporting on the localisation of single touches on the skin, and the other on the distance perception of dual touches. Participants were touched with two points, delivered either simultaneously or separated by a short delay to various locations on their left hand dorsum. They then indicated on a size-matched hand silhouette the perceived locations of tactile stimuli. We quantified the deviations between the actual stimulus grid and the corresponding perceptual map which was constructed from the perceived tactile locations, and we calculated the precision of tactile localisation (i.e. the variability across localisation attempts). The evidence showed that the dual touches, akin to single touch stimulations, were mislocalised distally and that their variable localisation error was reduced near joints, particularly near knuckles. However, contrary to single-touch localisation literature, we observed for the dual touches to be mislocalised towards the ulnar side of the hand, particularly when they were presented sequentially. Further, the touches presented in a sequential order were slightly ‘repelled’ from each other and their perceived distance increased, while the simultaneous tactile pairs were localised closer to each other and their distance was compressed. Whereas the sequential touches may have been localised with reference to the body, the compression of tactile perceptual space for simultaneous touches was related in the previous literature to signal summation and inhibition and the low-level factors, including the innervation density and properties of receptive fields of somatosensory neurons

Distortions of perceived volume and length of body parts

We experience our body as a 3D, volumetric object in the world. Measures of our conscious body image, in contrast, have investigated the perception of body size along one or two dimensions at a time. There is, thus, a discrepancy between existing methods for measuring body image and our subjective experience of having 3D body. Here we assessed in a sample of healthy adults the perception of body size in terms of its 1D length and 3D volume. Participants were randomly assigned to two groups using different measuring units (other body part and non-body object). They estimated how many units would fit in a perceived size of body segments and the whole body. The patterns of length and volume misperception across judged segments were determined as their perceived size proportional to their actual size. The pattern of volume misperception paints the representation of 3D body proportions resembling those of a somatosensory homunculus. The body parts with a smaller actual surface area relative to their volume were underestimated more. There was a tendency for body parts underestimated in volume to be overestimated in length. Perceived body proportions thus changed as a function of judgement type while showing a similarity in magnitude of the absolute estimation error, be it an underestimation of volume or overestimation of length. The main contribution of this study is assessing the body image as a 3D body representation, and thus extending beyond the conventional ‘allocentric’ focus to include the body on the inside. Our findings highlight the value of studying the perceptual distortions “at the baseline”, i.e. in healthy population, so as to advance the understanding of the nature of perceptual distortions in clinical conditions