Abstract

Synchronization of spatially distributed neural assemblies at frequencies in the range 30–70 Hz (the “gamma” band) may be instrumental in grouping stimulus features. In agreement with this we have shown that detection reaction times to a grouping target stimulus are expedited when the stimulus is preceded by repeated presentation of a priming stimulus, presented below detection thresholds in a matrix that flickers at particular frequencies in the 27–68 Hz range. This dynamic priming effect can be partly explained as a function of the return phase of the priming stimulus relative to the premask matrix, indicating one of the primary consequences of repeating stimulation is pre-activation of a priming response relative to prime-stimulus presentation. However, this cannot entirely explain the relationship that develops between the timing of stimulus events (in this instance the time of target relative to priming-stimulus presentations) and response. By varying the frequency and phase of priming-stimulus and target presentations we discovered that given a particular relationship between the phase of target presentation relative to the return phase of the prime, target coding is expedited by a prime that achieves its maximum activation at a phase that would precede priming-stimulus presentation by several tens of milliseconds. However, and in addition, the cognition concerned is flexible enough to be able to achieve an identical prime retroactively, that is to say at a phase during or subsequent to priming-stimulus presentation. This occurs because of a different relationship between the phase of target presentation (defined relative to prime frequency) and the frequency of premask-matrix presentation. On this basis, it can be concluded that by virtue of the relationship between its dynamics and the timing of stimulus events, microstructural cognition functions in a temporal context that can shift from past to future states. Consequently and at the lowest level of psychological function, the conventional, one-dimensional model of time flow—from future to past states does not fully explain how cognition can function. In fact depending upon the interaction in phase between different coding frequencies, the same form of cognition can anticipate or retroactively code events. Consequently, and in so far as our cognition at this level provides a content structure for consciousness, our psychological lives may be fundamentally based upon the ability of our cognitive states to travel backwards and forwards across very short intervals of time.

Highlights

  • The rhythmic synchronization of neural activity at gamma-band frequencies (30–70 Hz) is believed to be related to the organization of visual events, in particular the binding of individual visual features to form perceptual wholes (Gray, 1999; Singer, 1999)

  • Error reaction times (RTs) tended to be slower overall than correct RTs, and analysis of the probability correct by RT revealed no significant correlation between RT and accuracy, which argues against the correct data being contaminated by accuracy-speed trade-offs

  • A Kolmogorov “D” test showed RT distributions to be approximately lognormal and on this basis subsequent analyses were conducted on the exponents of the means of logtransformed RT distributions

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Summary

Introduction

The rhythmic synchronization of neural activity at gamma-band frequencies (30–70 Hz) is believed to be related to the organization of visual events, in particular the binding of individual visual features to form perceptual wholes (Gray, 1999; Singer, 1999). Taking into account critiques that challenge the necessity and sufficiency of some synchronization paradigms (Farid, 2002; Elliott et al, 2006b), there are a class of paradigms that have employed stimulus synchronizations presented below detection thresholds which prime or bring about the Gestalt organization of the synchronized stimulus elements (Elliott and Müller, 1998; Usher and Donnelly, 1998) These studies acknowledge a large body of evidence indicating that elements of a visual scene are often bound ahead of attentional deployment and are very unlikely to be coded by the same mechanisms as those mediating direct conscious experience of the Gestalt (e.g., Duncan and Humphreys, 1989; Rensink and Enns, 1995; Driver et al, 2001). Observers could not detect the presence of the premask grouping and because presentation of this stimulus does not cue target presentation, it is referred to as a prime

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