Visually induced gamma-band responses in human electroencephalographic activity — a link to animal studies

Visual presentation of an object produces firing patterns in cell assemblies representing the features of the object. Based on theoretical considerations and animal experiments, it has been suggested that the binding of neuronal representations of the various features is achieved through synchronization of the oscillatory firing patterns. The present study demonstrates that stimulus-induced gamma-band responses can be recorded non-invasively from human subjects attending to a single moving bar. This finding indicates the synchronization of oscillatory activity in a large group of cortical neurons. Gamma-band responses were not as apparent in the presence of two independently moving stimuli, suggesting that the neuronal activity patterns of different objects are not synchronized. These results open a new paradigm for investigating the mechanisms of feature binding and association building in relation to subjective perception.

[1]  Dennis Gabor,et al.  Theory of communication , 1946 .

[2]  P. Milner A model for visual shape recognition. , 1974, Psychological review.

[3]  M. B. Priestley,et al.  Non-linear and non-stationary time series analysis , 1990 .

[4]  W. Singer,et al.  Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties , 1989, Nature.

[5]  Reinhard Eckhorn,et al.  Feature Linking via Synchronization among Distributed Assemblies: Simulations of Results from Cat Visual Cortex , 1990, Neural Computation.

[6]  P König,et al.  Direct physiological evidence for scene segmentation by temporal coding. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[7]  W. Singer,et al.  Interhemispheric synchronization of oscillatory neuronal responses in cat visual cortex , 1991, Science.

[8]  P König,et al.  Synchronization of oscillatory neuronal responses between striate and extrastriate visual cortical areas of the cat. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[9]  W. Singer,et al.  Oscillatory Neuronal Responses in the Visual Cortex of the Awake Macaque Monkey , 1992, The European journal of neuroscience.

[10]  M. Young,et al.  On oscillating neuronal responses in the visual cortex of the monkey. , 1992, Journal of neurophysiology.

[11]  W. Singer,et al.  Temporal coding in the visual cortex: new vistas on integration in the nervous system , 1992, Trends in Neurosciences.

[12]  M. Tovée,et al.  Oscillatory activity is not evident in the primate temporal visual cortex with static stimuli , 1992, Neuroreport.

[13]  Robert Galambos,et al.  A Comparison of Certain Gamma Band (40-HZ) Brain Rhythms in Cat and Man , 1992 .

[14]  F. Varela,et al.  Visually Triggered Neuronal Oscillations in the Pigeon: An Autocorrelation Study of Tectal Activity , 1993, The European journal of neuroscience.

[15]  K. Reinikainen,et al.  Selective attention enhances the auditory 40-Hz transient response in humans , 1993, Nature.

[16]  B. Feige,et al.  Oscillatory brain activity during a motor task. , 1993, Neuroreport.

[17]  Shie Qian,et al.  Discrete Gabor transform , 1993, IEEE Trans. Signal Process..

[18]  S. Makeig Auditory event-related dynamics of the EEG spectrum and effects of exposure to tones. , 1993, Electroencephalography and clinical neurophysiology.

[19]  S. Zeki A vision of the brain , 1993 .

[20]  T. Elbert,et al.  Relationship of transient and steady-state auditory evoked fields. , 1993, Electroencephalography and clinical neurophysiology.

[21]  R. Eckhorn,et al.  High frequency (60-90 Hz) oscillations in primary visual cortex of awake monkey. , 1993, Neuroreport.

[22]  Werner Lutzenberger,et al.  Gamma-Band responses reflect word/pseudoword processing , 1994 .

[23]  K. H. Britten,et al.  Power spectrum analysis of bursting cells in area MT in the behaving monkey , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[24]  S Makeig,et al.  Different event-related patterns of gamma-band power in brain waves of fast- and slow-reacting subjects. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[25]  J. Prechtl,et al.  Visual motion induces synchronous oscillations in turtle visual cortex. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[26]  J. Pernier,et al.  Gamma‐range Activity Evoked by Coherent Visual Stimuli in Humans , 1995, The European journal of neuroscience.

[27]  Roman Bauer,et al.  Different rules of spatial summation from beyond the receptive field for spike rates and oscillation amplitudes in cat visual cortex , 1995, Brain Research.

[28]  W. Singer,et al.  Relation between oscillatory activity and long-range synchronization in cat visual cortex. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[29]  T. Elbert,et al.  Visual stimulation alters local 40-Hz responses in humans: an EEG-study , 1995, Neuroscience Letters.

[30]  W Singer,et al.  Visual feature integration and the temporal correlation hypothesis. , 1995, Annual review of neuroscience.

[31]  F. Rösler,et al.  Stimulus-induced gamma oscillations: harmonics of alpha activity? , 1995, Neuroreport.

[32]  Ch. von der Malsburg,et al.  A neural cocktail-party processor , 1986, Biological Cybernetics.

[33]  R. Eckhorn,et al.  Coherent oscillations: A mechanism of feature linking in the visual cortex? , 1988, Biological Cybernetics.