Topography and homogeneity of monkey VI studied through subdurally recorded pattern-evoked potentials

1989 ◽  
Vol 3 (6) ◽  
pp. 509-525 ◽  
Author(s):  
Gislin Dagnlie ◽  
Henk Spekreijse ◽  
Bob van Dijk

AbstractUsing small checkerboard stimulus fields, we have recorded visually evoked potentials (VEPs) in an alert rhesus monkey from an array of 35 electrodes chronically implanted between dura and arachnoid to study mass neuronal activity in striate and peristriate visual cortex. Although the principal purpose of this work was to study in detail cortical mapping in this particular animal for future intracortical recordings, we report here the usefulness of our approach for the non-invasive study of cortical processing, in particular of cortical magnification and receptive-field properties over the central 6° of the visual field.The striate and extrastriate components in the pattern onset VEP both have a double negative-going waveform, with N–P–N peak latencies of 75–100–135 ms and 90–115–160 ms, respectively, for small element sizes and moderate contrasts; latencies may be 5 ms shorter for large element sizes and high contrast. We found little activity at electrode locations over visual areas beyond V2. The waveforms and timing permit some careful speculation concerning intracortical processing and VEP generation.The complex logarithmic form of the retinotopical projection provides a satisfactory model for our data, if a value of 1–1.2° is used for the offset parameter a. Our data suggest that the most abundant receptive-field size in foveal striate cortex has a center diameter of 12′. This size remains constant up to 2° eccentricity, and increases only slowly up to 4°. The smallest receptive-field sizes seem to be independent of eccentricity, throughout the central 4° of Vl, with a value of 4–8′, in agreement with single-cell data reported by Dow et al. (1981) and Van Essen et al. (1984).

1990 ◽  
Vol 2 (1) ◽  
pp. 71-84 ◽  
Author(s):  
Kamil A. Grajski ◽  
Michael M. Merzenich

The inverse magnification rule in cortical somatotopy is the experimentally derived inverse relationship between cortical magnification (area of somatotopic map representing a unit area of skin surface) and receptive field size (area of restricted skin surface driving a cortical neuron). We show by computer simulation of a simple, multilayer model that Hebb-type synaptic modification subject to competitive constraints is sufficient to account for the inverse magnification rule.


1986 ◽  
Vol 55 (6) ◽  
pp. 1136-1152 ◽  
Author(s):  
C. L. Baker ◽  
M. S. Cynader

Responses of direction-selective neurons in cat striate cortex (area 17) were studied with flashed-bar stimuli. Spatial parameters of interactions within the receptive field giving rise to direction selectivity and of receptive-field subunits were quantitatively determined for the same cells and correlated. A bar stimulus flashed sequentially at two nearby locations in the receptive field produced direction-selective behavior comparable with that elicited by continuously moving stimuli. Each cell exhibited a characteristic optimal spatial displacement, Dopt, for which responses in the presumed preferred and null directions were maximally distinct. In all cases, Dopt was much smaller than the receptive-field size. The spatial structure of receptive fields in simple cells was studied using single narrow-bar stimuli flashed at different locations in the receptive field. The resulting line-weighting function exhibited alternating regions of ON and OFF responses having a characteristic spatial period or wavelength, lambda. Spatial subunit structure in complex cells was determined by flashing two bars simultaneously in the receptive field. The response as a function of bar separation was again a wavelike function having a spatial wavelength, lambda. Values of the optimal displacement for direction selectivity, Dopt, showed a clear relationship with the spatial wavelength, lambda, for a given unit. Dopt was also correlated to a somewhat lesser degree with receptive-field size. Generally, the ratio of Dopt to lambda was approximately 1/10 to 1/4, in agreement with theoretical predictions by Marr and Poggio. Taken together with the findings of Movshon et al., these results indicate a systematic relationship between Dopt and the spatial frequency of a sinusoidal grating, which is optimal for that cell. Such a relationship is consistent with the results of human psychophysical experiments on apparent motion.


2017 ◽  
Vol 17 (10) ◽  
pp. 587
Author(s):  
Ben Harvey ◽  
Jan Brascamp ◽  
Sónia Ferreira ◽  
Miguel Castelo-Branco ◽  
Serge Dumoulin ◽  
...  

1999 ◽  
Vol 39 (3) ◽  
pp. 613-629 ◽  
Author(s):  
Ute Bauer ◽  
Michael Scholz ◽  
Jonathan B. Levitt ◽  
Klaus Obermayer ◽  
Jennifer S. Lund

NeuroImage ◽  
2018 ◽  
Vol 167 ◽  
pp. 41-52 ◽  
Author(s):  
Maria Fatima Silva ◽  
Jan W. Brascamp ◽  
Sónia Ferreira ◽  
Miguel Castelo-Branco ◽  
Serge O. Dumoulin ◽  
...  

1988 ◽  
Vol 59 (5) ◽  
pp. 1557-1574 ◽  
Author(s):  
C. L. Baker

1. Direction-selective properties of neurons in cat striate cortex (area 17) were studied with flashed and continuously moving bar stimuli. Receptive fields were characterized by measurement of static and dynamic parameters, which were correlated with the velocity preference exhibited by the same cells. 2. Each neuron was found to be direction selective to a limited range of velocities. This behavior was characterized by measuring the optimal velocity (Vopt) to elicit responses in the preferred and null directions that were maximally distinct. 3. A bar stimulus flashed sequentially at two nearby locations in the receptive field also produced direction-selective behavior, which was characterized by an optimal displacement (Dopt) to drive maximally distinct responses in the preferred versus null directions. 4. The static spatial receptive field properties were quantified by measurement of the receptive field size (2 sigma) and the spatial subunit wavelength (lambda). The latter quantity was measured as twice the separation between adjacent ON and OFF regions in simple cells and as twice the optimal separation for lateral inhibition between two simultaneously flashed bars in complex cells. 5. Direction-selective velocity preference for continuously moving stimuli, Vopt, was found to be highly correlated with lambda and with the Dopt for 2-flash motion; Vopt was also correlated to a lesser degree with 2 sigma. These results suggest a fundamental linkage between spatial frequency preference, velocity preference, and spatial tuning to 2-flash motion. 6. The range of measured direction-selective velocity preference values (Vopt) spanned about a 100-fold range, whereas the corresponding values of Dopt or lambda spanned substantially smaller ranges. This discrepancy suggested that the dynamic range of velocity preference among cortical neurons might be determined jointly by the measured spatial properties and by a temporal property that covaries with the measured spatial properties. 7. Temporal properties of striate cortical neurons were assessed from responses to flashed stimuli having a prolonged duration ("step responses"). Neurons typically responded in the following manner: after some latency (L), a transient rise in spike frequency occurred, which then adapted to some sustained level. The adaptation dynamics (extent of sustained vs. transient behavior) were quantified by the first-order time constant (AT) of the adaptation decay, and by the ratio of initial transient rise to final sustained level [adaptation ratio (AR)].(ABSTRACT TRUNCATED AT 400 WORDS)


1976 ◽  
Vol 39 (6) ◽  
pp. 1288-1319 ◽  
Author(s):  
P. H. Schiller ◽  
B. L. Finlay ◽  
S. F. Volman

1. The properties of single cells in striate cortex of the rhesus monkey, representing the visual field 2 degrees -5 degrees from the fovea, were examined quantitatively with stationary and moving stimuli. Three distinct classes of cells were identified: S type, CX type, and T type. 2. S-type cells were defined as those oriented cells which to the optimal direction of movement in their receptive fields exhibited one or more spatially separate subfields within each of which a response was obtained to either a light or dark edge, but not to both. Several different types of S-cells were distinguished: a) S1-type cells for which moving edges revealed a single excitatory area within which a response was elicited by either a light or a dark edge but not by both. Most of these cells were unidirectional. b) S2-type cells for which moving edges revealed two spatially separate response areas, one of which was excited by a light edge and the other by a dark edge. Both regions responded to the same direction of movement. c) S3-type cells which had two response areas, one of which was excited by a stimulus moving in one direction (at right angles to the axis of orientation) and the other, of opposite contrast, which responded in the opposite direction, d) S4-type cells which to one direction of movement showed two spatially separate regions sensitive to a light and dark edge and which in the other direction of movement had only one responsive area (either light or dark). e) Cells which had multiple spatially separate subfields (S5-7 types). 3. CX-type cells were defined as those oriented cells which in their receptive fields exhibited no spatial separation for light- and dark-edge responses; they discharged to both edges in the same direction of movement and in the same spatial area. Flashing stimuli elicited both on and off responses throughout the receptive field. CX-type cells were predominantly of two types: those which were selective for direction of stimulus movement and those which were not. 4. A third class of cells (T-type) were those which were excited by only one sign of contrast change and responded in a sustained fashion even when there was no contour within the receptive field. These cells were poorly or not at all oriented; some of them were selective to wavelength. 5. Quantitative comparisons showed the following differences between S-type and CX-type cells: a) S-type cells had smaller receptive fields than CX-type cells but the populations over-lapped considerably. Receptive-field size was smallest in layer 4c. In all other layers S-type cells had the same size fields. CX-type cells, by contrast, tended to have larger fields in layer 5-6 than 2-3. b) The spatial separation between light and dark response areas was the best criterion for distinguishing S-type and CX-type cells. The distribution of this measure disclosed two populations of cells with relatively limited overlap. c) In layers 2 and 3, both S-type and CX-type cells had low spontaneous activity…


Sign in / Sign up

Export Citation Format

Share Document