19,709 research outputs found
On the stimulus duty cycle in steady state visual evoked potential
Brain-computer interfaces (BCI) are useful devices that allow direct control of external devices using thoughts, i.e. brain's electrical activity. There are several BCI paradigms, of which steady state visual evoked potential (SSVEP) is the most commonly used due to its quick response and accuracy. SSVEP stimuli are typically generated by varying the luminance of a target for a set number of frames or display events. Conventionally, SSVEP based BCI paradigms use magnitude (amplitude) information from frequency domain but recently, SSVEP based BCI paradigms have begun to utilize phase information to discriminate between similar frequency targets. This paper will demonstrate that using a single frame to modulate a stimulus may lead to a bi-modal distribution of SSVEP as a consequence of a user attending both transition edges. This incoherence, while of less importance in traditional magnitude domain SSVEP BCIs becomes critical when phase is taken into account. An alternative modulation technique incorporating a 50% duty cycle is also a popular method for generating SSVEP stimuli but has a unimodal distribution due to user's forced attention to a single transition edge. This paper demonstrates that utilizing the second method results in significantly enhanced performance in information transfer rate in a phase discrimination SSVEP based BCI
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Hearing through your eyes: neural basis of audiovisual cross-activation, revealed by transcranial alternating current stimulation
Some people experience auditory sensations when seeing visual flashes or movements. This prevalent synaesthesia-like ‘visual-evoked auditory response’ (vEAR) could result either from over-exuberant cross-activation between brain areas, and/or reduced inhibition of normally-occurring cross-activation. We have used transcranial alternating current stimulation (tACS) to test these theories. We applied tACS at 10Hz (alpha-band frequency) or 40Hz (gamma-band), bilaterally either to temporal or occipital sites, while measuring same/different discrimination of paired auditory (A) versus visual (V) 'Morse code' sequences. At debriefing, participants were classified as vEAR or non-vEAR depending on whether they reported 'hearing' the silent flashes.
In non-vEAR participants, temporal 10Hz tACS caused impairment of A performance, which correlated with improved V; conversely under occipital tACS, poorer V performance correlated with improved A. This reciprocal pattern suggests that sensory cortices are normally mutually inhibitory, and that alpha-frequency tACS may bias the balance of competition between them. vEAR participants showed no tACS effects, consistent with reduced inhibition, or enhanced cooperation between modalities. In addition, temporal 40Hz tACS impaired V performance, specifically in individuals who showed a performance advantage for V (relative to A). Gamma-frequency tACS may therefore modulate the ability of these individuals to benefit from recoding flashes into the auditory modality, possibly by disrupting cross-activation of auditory areas by visual stimulation.
Our results support both theories, suggesting that vEAR may depend on disinhibition of normally-occurring sensory cross-activation, which may be expressed more strongly in some individuals. Furthermore, endogenous alpha and gamma-frequency oscillations may function respectively to inhibit or promote this cross-activation
Aerospace Medicine and Biology: A continuing bibliography with indexes, supplement 127, April 1974
This special bibliography lists 279 reports, articles, and other documents introduced into the NASA scientific and technical information system in March 1974
Change blindness: eradication of gestalt strategies
Arrays of eight, texture-defined rectangles were used as stimuli in a one-shot change blindness (CB) task where there was a 50% chance that one rectangle would change orientation between two successive presentations separated by an interval. CB was eliminated by cueing the target rectangle in the first stimulus, reduced by cueing in the interval and unaffected by cueing in the second presentation. This supports the idea that a representation was formed that persisted through the interval before being 'overwritten' by the second presentation (Landman et al, 2003 Vision Research 43149–164]. Another possibility is that participants used some kind of grouping or Gestalt strategy. To test this we changed the spatial position of the rectangles in the second presentation by shifting them along imaginary spokes (by ±1 degree) emanating from the central fixation point. There was no significant difference seen in performance between this and the standard task [F(1,4)=2.565, p=0.185]. This may suggest two things: (i) Gestalt grouping is not used as a strategy in these tasks, and (ii) it gives further weight to the argument that objects may be stored and retrieved from a pre-attentional store during this task
Aerospace Medicine and Biology: A continuing bibliography with indexes (supplement 314)
This bibliography lists 139 reports, articles, and other documents introduced into the NASA scientific and technical information system in August, 1988
Aerospace Medicine and Biology: A continuing supplement 180, May 1978
This special bibliography lists 201 reports, articles, and other documents introduced into the NASA scientific and technical information system in April 1978
Neutral coding - A report based on an NRP work session
Neural coding by impulses and trains on single and multiple channels, and representation of information in nonimpulse carrier
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