Haptic memory

Perhaps the first experiment conducted to study the phenomenon of haptic memory was that of Bliss, Crane, Mansfield, and Townsend who investigated the characteristics of immediate recall for brief tactile stimuli applied to the hand. The results obtained showed a haptic memory store remarkably similar to the visual memory store suggested by Sperling in 1960, with a capacity of approximately four to five items. Similar to tests of visual sensory memory, it was also found that haptic memory performance was significantly improved with the use of partial report procedures. This particular finding is consistent with more recent research by Gallace in 2008. Bliss et al. interpreted this difference in partial report versus whole report as a sensory form of memory for passively presented tactile stimuli with a high capacity and short duration. Additional support for the short duration of haptic memory comes from studies by Gilson and Baddeley in 1969. According to these studies, memory for stimuli applied to the skin is resilient for approximately ten seconds after removal of the stimulus, even when the individual is engaged in tasks that inhibit verbal rehearsal. After this delay, the memory trace becomes vulnerable to forgetting as it decays from the haptic memory store and begins to rely on a more central memory store. Similar findings were later reported by Miles and Borthwick in 1996, who emphasized the role of tactile interference on discriminability of the target location and the role of central processing resources in consolidation of haptic memory. More recent experimental procedures and technologies such as minielectrode recording devices and transcranial magnetic stimulation have allowed for mapping of brain areas involved in the storage of tactile memories. Implicated in most of these studies is the primary somatosensory cortex. More recent studies have also investigated a broader selection of participants, allowing for the discovery of an intact haptic memory in infants. ==Neuroanatomy==

Tactile memories are organized somatotopically, following the organization of the somatosensory cortex. This means that areas close on the body surface receive nervous signals from areas that are close together on the brain surface. Several distinct areas of the parietal lobe are responsible for contributing to different aspects of haptic memory. Memory for the properties of stimuli such as roughness, spatial density, and texture involves activation of the parietal operculum. Properties of stimuli such as size and shape, as detected by touch receptors in the skin, are stored in the anterior part of the parietal lobe. Memory for spatial information such as the location of stimuli involves the right superior parietal lobule and temporoparietal junction. Additional neuroimaging data has been provided by studies using microelectrodes implanted in the somatosensory cortex of monkeys. When performing a delayed match to sample task with objects of identical dimensions but different surface features, activity is observed in somatosensory neurons during perception and in the short-term memory for tactile stimuli. ==Development==

Memory is important in infancy as it forms the basis for more complex procedures such as learning and reasoning. Studies of haptic memory in infants is particularly useful because it allows researchers to study the more perceptual representation of information as opposed to verbal or semantic aspects. Haptic abilities develop in stages in infants: Furthermore, it is proven that our haptic cues and memory affects our visual experience and the two experiences are linked for us to comprehend our surroundings. ==Implicit==

Implicit memory can be referred to as the subconscious recollection of previously presented information. This type of memory influences one's actions and behaviors without the individual having any awareness of its availability for explicit recall. Implicit memory has been linked to phenomena such as skill acquisition, priming, and classical conditioning. In some cases, tactile information is also remembered implicitly. Evidence for this comes from patients with damage to the right cerebral hemisphere, who, due to their brain damage, are unable to explicitly report any of the qualities of objects held in their left hand when another object is simultaneously presented in their right hand. Despite this fact, when the patients are asked to compare the characteristics of objects presented to either hand, their judgements are influenced by objects previously held in their right hand. This suggests that the patients have some memory for the properties of objects recently removed from their right hand that they are not consciously aware of, and that this memory is affecting their accuracy on subsequent tasks. Similar evidence has been found in healthy individuals of varying ages, and in patients with Alzheimer's disease. ==See also==