The role of the somatosensory system in the feeling of emotions: a neurostimulation study.

Emotional experiences deeply impact our bodily states, such as when we feel 'anger', our fists close and our face burns. Recent studies have shown that emotions can be mapped onto specific body areas, suggesting a possible role of the primary somatosensory system (S1) in emotion processing. To date, however, the causal role of S1 in emotion generation remains unclear.

Visual perceptual learning is enhanced by training in the illusory far space.

Visual objects in the peripersonal space (PPS) are perceived faster than farther ones appearing in the extrapersonal space (EPS). This shows preferential processing for visual stimuli near our body. Such an advantage should favour visual perceptual learning occurring near, as compared with far from observers, but opposite evidence has been recently provided from online testing protocols, showing larger perceptual learning in the far space.

Visual perceptual learning is effective in the illusory far but not in the near space.

Visual shape discrimination is faster for objects close to the body, in the peripersonal space (PPS), compared with objects far from the body. Visual processing enhancement in PPS occurs also when perceived depth is based on 2D pictorial cues. This advantage has been observed from relatively low-level (detection, size, orientation) to high-level visual features (face processing).

Size Constancy Mechanisms: Empirical Evidence from Touch.

Several studies have shown the presence of large anisotropies for tactile distance perception across several parts of the body. The tactile distance between two touches on the dorsum of the hand is perceived as larger when they are oriented mediolaterally (across the hand) than proximodistally (along the hand). This effect can be partially explained by the characteristics of primary somatosensory cortex representations.

Tactile distance anisotropy on the feet.

Perception of distance between two touches varies with orientation on the hand, with distances aligned with hand width perceived as larger than those aligned with hand length. Similar anisotropies are found on other body parts (e.g.

Whole-hand perceptual maps of joint location.

Hands play a fundamental role in everyday behaviour. Nevertheless, healthy adults show striking misrepresentations of their hands which have been documented by a wide range of studies addressing various aspects of body representation. For example, when asked to indicate the location within the hand of the knuckles, people place them substantially farther forward than they actually are.

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.

Tactile interactions in the path of tactile apparent motion.

Perceptual completion is a fundamental perceptual function serving to maintain robust perception against noise. For example, we can perceive a vivid experience of motion even for the discrete inputs across time and space (apparent motion: AM). In vision, stimuli irrelevant to AM perception are suppressed to maintain smooth AM perception along the AM trajectory where no physical inputs are applied.

Fingers hold spatial information that toes do not.

Fingers have preferential associations with relative spatial locations. Tactile localisation is faster when the fingers are in these locations, such as when the index finger is in a relatively higher spatial position, and the thumb in a relatively lower position. However, it is unclear whether these associations are related to hands specifically, or are a more general characteristic of limbs.

Anisotropy in tactile time perception.

Spatial distortions in touch have been investigated since the 19th century. For example, two touches applied to the hand dorsum feel farther apart when aligned with the mediolateral axis (i.e.

Structural representations of fingers rely on both anatomical and spatial reference frames.

Finger agnosia refers to a neurological condition in which patients with left posterior parietal lesions fail to identify their fingers, despite having relatively preserved abilities in sensation and skilled action. This dissociation suggests that the structural body representations (BSRs) may be distinct from sensorimotor representations. However, recent research has reported that postural changes modulate representation of hand structure, revealing dynamic interactions between structural and sensorimotor body representations.

A common representation of fingers and toes.

There are many similarities and differences between the human hands and feet. On a psychological level, there is some evidence from clinical disorders and studies of tactile localisation in healthy adults for deep functional connections between the hands and feet. One form these connections may take is in common high-level mental representations of the hands and feet.

The standard posture of the hand.

Perceived limb position is known to rely on sensory signals and motor commands. Another potential source of input is a standard representation of body posture, which may bias perceived limb position toward more stereotyped positions. Recent results show that tactile stimuli are processed more efficiently when delivered to a thumb in a relatively low position or an index finger in a relatively high position.

A Conceptual Model of Tactile Processing across Body Features of Size, Shape, Side, and Spatial Location.

The processing of touch depends of multiple factors, such as the properties of the skin and type of receptors stimulated, as well as features related to the actual configuration and shape of the body itself. A large body of research has focused on the effect that the nature of the stimuli has on tactile processing. Less research, however, has focused on features beyond the nature of the touch.

Locating primary somatosensory cortex in human brain stimulation studies: experimental evidence.

Transcranial magnetic stimulation (TMS) over human primary somatosensory cortex (S1) does not produce immediate outputs. Researchers must therefore rely on indirect methods for TMS coil positioning. The "gold standard" is to use individual functional and structural magnetic resonance imaging (MRI) data, but the majority of studies don't do this.

Locating primary somatosensory cortex in human brain stimulation studies: systematic review and meta-analytic evidence.

Transcranial magnetic stimulation (TMS) over human primary somatosensory cortex (S1), unlike over primary motor cortex (M1), does not produce an immediate, objective output. Researchers must therefore rely on one or more indirect methods to position the TMS coil over S1. The "gold standard" method of TMS coil positioning is to use individual functional and structural magnetic resonance imaging (f/sMRI) alongside a stereotactic navigation system.

Dissociation of feeling and belief in the rubber hand illusion.

The Rubber Hand Illusion (RHI) has been widely used to investigate the perception of the bodily self. Commonly used measures of the illusion are self-report questionnaires and proprioceptive drift of the participants' hands towards the rubber hand. Recent studies have shown that these measures can be dissociated, suggesting they may arise from distinct mechanisms.

More than skin-deep: Integration of skin-based and musculoskeletal reference frames in localization of touch.

The skin of the forearm is, in one sense, a flat 2-dimensional (2D) sheet, but in another sense approximately cylindrical, mirroring the 3-dimensional (3D) volumetric shape of the arm. The role of frames of reference based on the skin as a 2D sheet versus based on the musculoskeletal 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.

Tactile confusions of the fingers and toes.

Recent research has shown systematic patterns of confusions between digits of the hands and feet. The present study addressed whether such confusions arise from early somatosensory maps or higher level body representations. As the glabrous and hairy skin of the hands and feet have distinct representations in somatosensory cortex, an effect arising from early somatotopic maps may show distinct patterns on each skin surface.

Multisensory Perception: Magnetic Disruption of Attention in Human Parietal Lobe.

Paying attention to sounds and touches at the same time is demanding. New research shows how the parietal lobe of the human brain mediates multisensory perception of stimulus frequency and intensity.

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 localization 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.

Conceptual distortions of hand structure are robust to changes in stimulus information.

Previous studies showed stereotyped distortions in hand representations. People judge their knuckles as farther forward in the hand than they actually are. The cause of this bias remains unclear.

Tactile localization biases are modulated by gaze direction.

Identifying the spatial location of touch on the skin surface is a fundamental function of our somatosensory system. Despite the fact that stimulation of even single mechanoreceptive afferent fibres is sufficient to produce clearly localised percepts, tactile localisation can be modulated also by higher level processes such as body posture. This suggests that tactile events are coded using multiple representations using different coordinate systems.

Vision of the body improves inter-hemispheric integration of tactile-motor responses.

Sensory input from and motor output to the two sides of the body needs to be continuously integrated between the two cerebral hemispheres. This integration can be measured through its cost in terms of processing speed. In simple detection tasks, reaction times (RTs) are faster when stimuli are presented to the side of the body ipsilateral to the body part used to respond.