Spatial component analysis is often used to explore multidimensional time series data whose sources cannot be measured directly. Several methods may be used to decompose the data into a set of spatial components with temporal loadings. Component selection is of crucial importance, and should be supported by objective criteria. In some applications, the use of a well defined component selection criterion may provide for automation of the analysis. In this paper we describe a novel approach for ranking of spatial components calculated from the EEG or MEG data recorded within evoked response paradigm. Our method is called Mutual Information (MI) Spectrum and is based on gauging the amount of MI of spatial component temporal loadings with a synthetically created reference signal. We also describe the appropriate randomization based statistical assessment scheme that can be used for selection of components with statistically significant amount of MI. Using simulated data with realistic trial to trial variations and SNR corresponding to the real recordings we demonstrate the superior performance characteristics of the described MI based measure as compared to a more conventionally used power driven gauge. We also demonstrate the application of the MI Spectrum for the selection of task-related independent components from real MEG data. We show that the MI spectrum allows to identify task-related components reliably in a consistent fashion, yielding stable results even from a small number of trials. We conclude that the proposed method fits naturally the information driven nature of ICA and can be used for routine and automatic ranking of independent components calculated from the functional neuroimaging data collected within event-related paradigms.

Detection of illusory contours (ICs) such as Kanizsa figures is known to depend primarily upon the lateral occipital complex. Yet there is no universal agreement on the role of the primary visual cortex in this process; some existing evidence hints that an early stage of the visual response in V1 may involve relative suppression to Kanizsa figures compared with controls. Iso-oriented luminance borders, which are responsible for Kanizsa illusion, may evoke surround suppression in V1 and adjacent areas leading to the reduction in the initial response to Kanizsa figures. We attempted to test the existence, as well as to find localization and timing of the early suppression effect produced by Kanizsa figures in adult nonclinical human participants. We used two sizes of visual stimuli (4.5 and 9.0°) in order to probe the effect at two different levels of eccentricity; the stimuli were presented centrally in passive viewing conditions. We recorded magnetoencephalogram, which is more sensitive than electroencephalogram to activity originating from V1 and V2 areas. We restricted our analysis to the medial occipital area and the occipital pole, and to a 40-120 ms time window after the stimulus onset. By applying threshold-free cluster enhancement technique in combination with permutation statistics, we were able to detect the inverted IC effect-a relative suppression of the response to the Kanizsa figures compared with the control stimuli. The current finding is highly compatible with the explanation involving surround suppression evoked by iso-oriented collinear borders. The effect may be related to the principle of sparse coding, according to which V1 suppresses representations of inner parts of collinear assemblies as being informationally redundant. Such a mechanism is likely to be an important preliminary step preceding object contour detection.

The illusory contour is one of the most often used models in studies of Gestalt perception. In our MEG study we observed the so-called illusory contour effect (IC-effect): the activity of nonprimary visual and associative cortical areas was increased during the 150-250 ms time window after a stimulus onset in response to illusory stimulus, compared with the control stimulus. In addition to the positive IC-effect, the inverted IC-effect was revealed for the first time in adults. In our study it was manifested during the 60-120 ms window after the onset of stimulus. The inverted IC-effect is an early decrease in the activity of the visual cortex in response to the illusory contour compared with the control stimulus. The mechanism of the inverted IC-effect is yet unclear. The "bottom-up" and "top-down" hypotheses of the origin of the inverted IC-effect are discussed.

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