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L G Thorell

Publications and source records attributed to L G Thorell.

4 recordsLinked to original sources

Periodicity of striate-cortex-cell receptive fields.

If striate cells had the simple bipartite or tripartite receptive fields (RF's) classically attributed to them, they should be quite broadly tuned for spatial frequency. Most striate-cortex cells, however, are fairly narrowly tuned and would be expected to have more-periodic RF's. We have examined this question in recordings of the responses of cat and monkey striate-cortex cells to gratings of increasingly large number of cycles, all centered on the cells' RF's. Simple cells narrowly tuned for spatial frequency were found to increase their responses with increasing numbers of stimulus cycles beyond the 1 1/2 cycles expected from the classical RF shape. Broadly tuned simple cells were found to have less-periodic RF's. Whereas narrowly tuned complex cells were also found to respond maximally to many stimulus cycles, other more broadly tuned complex cells did as well (possibly reflecting summation across many broadly tuned simple cells without regard to phase). A suppressive region was often seen just outside the excitatory two-dimensional spatial-frequency region, at off orientations and/or off spatial frequencies and around the whole RF in space. Most striate cells can thus be described as having periodic RF's in the space domain such that they fire just to patterns whose local spatial-frequency spectra fall within a compact, restricted, roughly circular two-dimensional spatial-frequency region, with an encircling suppressive region in both the space and the frequency domains.

Animals↗

Spatial mapping of monkey V1 cells with pure color and luminance stimuli.

We recorded the responses of single macaque striate cortical cells to color-varying and luminance-varying patterns. We show that (a) the vast majority of primate striate cells respond to pure color stimuli, in addition to responding to luminance-varying stimuli (b) in general, simple cells are color-selective whereas complex cells respond to multiple color regions, (c) most cortical cells show bandpass spatial frequency tuning to pure color-varying gratings, with various cells tuned to each of a wide range of spatial frequencies and (d) the peak spatial frequency and bandwidth of most striate cells is the same for color as for luminance-varying gratings; when they differ, cells tend to be more broadly tuned and peak at lower spatial frequencies for color (e) complex cells, on the average, respond to higher spatial frequencies than do simple cells.

Animals↗

Spatial frequency selectivity of cells in macaque visual cortex.

We measured the spatial frequency contrast sensitivity of cells in the primate striate cortex at two different eccentricities to provide quantitative statistics from a large population of cells. Distributions of the peak frequencies and bandwidths are presented and examined in relationship to (a) each other, (b) absolute contrast sensitivity, (c) orientation tuning, (d)retinal eccentricity, and (e) cell type. Simple and complex cells are examined in relationship to linear/nonlinear (that is, X/Y) properties; a procedure is described which provides a simple, reliable and quantitative method for classifying and describing striate cells. Among other things, it is shown that (a) many stirate cells have quite narrow spatial bandwidths and (b) at a given retinal eccentricity, the distribution of peak frequency covers a wide range of frequencies; these findings support the basic multiple channel notion. The orientation tuning and spatial frequency tuning which occurs at the level of striate cortex (in a positively correlated fashion) suggests that the cells might best be considered as two-dimensional spatial filters.

Animals↗

Visual cortical neurons: are bars or gratings the optimal stimuli?

Neurons in the visual cortex of monkeys and cats have been characterized as either (i) bar and edge detectors or (ii) cells selective for certain spatial frequencies. To assess which of these functional descriptions is more accurate, we measured (i) the selectivity and (ii) the responsivity-sensitivity of these neurons to bars of various widths and gratings of various spatial frequencies. All of the cells recorded from were considerably more selective along the dimension of spatial frequency than along the dimension of bar width. Further, most were more responsive and sensitive to the grating of optimal frequency than to the bar of optimal width.

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