Stimulus-related synchronization,'visual binding' and signal-to-noise
ratio in the brain.
Walter G. Sannita
Department of Motor Science, University of Genova, Genova, Italy, and
Department of Psychiatry, State University of New York, Stony Brook, NY,
USA
Our visual system translates the external world into images and we
recognize and categorize objects. Usually referred to as 'visual binding',
the integration of visual features into coherent, three-dimensional
perceptual representations - an illusion forever builds into the brain
through experience – is a classic problem (“the binding problem”) and a
matter of debate [1]. Transient increase in the phase synchrony across
cortical areas is the critical process Melloni et al. suggest mediate in
the access to conscious perception [2]. This adds to the hypothesis that
synchronization and attentional selection are necessary for cortical
integration to occur and mediate in 'visual binding' [1]. Critics of the
bottom-up hypothesis argue that selective synchronization appears unlikely
based on neural computation and that whatever visual binding may be, it
seems unaffected when the primary visual areas are damaged. Some top-down
organization from non-primarily visual cortices is suggested, consistent
with the massive involvement of the primate brain in vision [1].
Observations from a neuromagnetic experiment on human vision [3] add to
the controversy. Meaningful words embedded in white dynamical noise were
presented with a stimulus signal-to-noise function across noise levels
that matched the "threshold-stochastic resonance" paradigm (threshold-SR)
[4]. As predicted, word recognition depended on the signal/noise
interaction; activation in primary cortex fitted the stimulus signal-to-
noise function. Unexpectedly, however, brain activation matched the
stimulus signal-to-noise function also in non-primary visual cortices and
at temporal-central brain sites where language processing is thought to
occur irrespective of the physical properties of visual input [3]. No
direct inference about visual binding is obviously possible based on this
observation. Yet, this transfer of the signal-to-noise function from
visual input to visual cortex to language areas is consistent with the
hypothetized bottom-up information processing [1]; implications in lower-
level brain function are also conceivable and would suggest some
compatibility with or intrinsic adaptation of brain processes to, the
threshold-SR function. Object recognition is likely to occur because ‘we
already have in the brain a model of that object and this model is
activated through vision' [4]. Some internal model fitting the signal-to-
noise function of the threshold-SR stimulus applied in this study
therefore does not appear implausible and would be in the line of evidence
that interaction between neuronal signalling and noise is ubiquitous in
the brain [5].
1.Neuron. 1999; 24, 7-127 (special review on visual binding).
2. Melloni L, Molina C, Pena M, Torres D, Singer W, Rodriguez E.
Synchronization of neural activity across cortical areas correlates with
conscious perception. J Neurosci. 2007;27:2858-2865.
3. Sorrentino A, Parkkonen L, Piana M, Massone AM, Narici L, Carozzo S,
Riani M, Sannita WG. Modulation of brain and behavioural responses to
cognitive visual stimuli with varying signal-to-noise ratios. Clin
Neurophysiol. 2006; 117: 1098-1105.
4. Wiesenfeld, K. and Moss, F. Stochastic resonance and the benefits of
noise: from ice ages to crayfish and SQUIDs. Nature 1995; 373: 33-36;
Gammaitoni L, Hanggi P, Jung P, Marchesoni F. Stochastic Resonance. Rev
Mod Phys 1998; 70:223 – 288; Moss F, Ward L, Sannita WG. Stochastic
resonance and sensory information processing: a tutorial and review of
application. Clin Neurophysiol, 115 : 267-281, 2004.
5. Ito M. Internal model visualized. Nature 2000; 403, 153-154