Cells in the cat's striate cortex show marked specificity in their responses to restricted retinal stimulation (Hubel & Wiesel, 1959, 1962). The most effective stimulus shapes are long narrow rectangles of light ('slits'), dark bars against a light background ('dark bars'), and straight-line borders separating areas of different brightness ('edges'). A given cell responds vigorously when an appropriate stimulus is shone on the receptive field or moved across it, provided the stimulus is presented in a specific orientation. This orientation is termed the 'receptive-field axis orientation'. It is critical, and constant for any particular cell, but may differ for different cells. The visual cortex is subdivided into discrete regions or columns extending from surface to white matter, in which all cells have the same receptivefield axis orientation (Hubel & Wiesel, 1962). The present experiments were undertaken with the object of learning more about the anatomical configuration of the columns. We wished to have a clearer idea of their shape, especially if the walls of a column were, as previous work suggested, parallel to the radial fibre bundles of the cortex and perpendicular to the cortical layers, and whether the columns were uniform or irregular in their cross-sectional shape and size. Furthermore, we were curious to know if there was any relationship between the receptive-field axis orientations of neighbouring columns, or whether, on the contrary, the different columns were intermixed in a random way throughout the cortex. These questions were approached: (1) by making several deep, closely spaced, parallel micro-electrode penetrations, placing electrolytic lesions at every shift in receptive-field orientation, and(2) by making many short penetrations in a small cortical area, noting the axis orientation of cells lying in the upper one or two layers of cortex.
[1]
P. W. Davies.
Chamber for microelectrode studies in the cerebral cortex.
,
1956,
Science.
[2]
D. Hubel.
Tungsten Microelectrode for Recording from Single Units.
,
1957,
Science.
[3]
V. Mountcastle.
Modality and topographic properties of single neurons of cat's somatic sensory cortex.
,
1957,
Journal of neurophysiology.
[4]
D. Hubel.
Single unit activity in striate cortex of unrestrained cats
,
1959,
The Journal of physiology.
[5]
D. Hubel,et al.
Receptive fields of single neurones in the cat's striate cortex
,
1959,
The Journal of physiology.
[6]
V. Mountcastle,et al.
Some aspects of the functional organization of the cortex of the postcentral gyrus of the monkey: a correlation of findings obtained in a single unit analysis with cytoarchitecture.
,
1959,
Bulletin of the Johns Hopkins Hospital.
[7]
D. Hubel,et al.
Receptive fields of optic nerve fibres in the spider monkey
,
1960,
The Journal of physiology.
[8]
D. Hubel,et al.
Integrative action in the cat's lateral geniculate body
,
1961,
The Journal of physiology.
[9]
D. Hubel,et al.
Receptive fields, binocular interaction and functional architecture in the cat's visual cortex
,
1962,
The Journal of physiology.