Literature DB >> 5157596

Responses to visual contours: spatio-temporal aspects of excitation in the receptive fields of simple striate neurones.

P O Bishop, J S Coombs, G H Henry.   

Abstract

1. The properties of the receptive fields of simple cells in the cat striate cortex have been studied by preparing average response histograms both to moving slits of light of different width and to single light-dark edges or contours.2. The movement of a narrow (< 0.3 degrees ) slit across the receptive field gives rise to average response histograms that are either unimodal, bimodal or multimodal. A slit of light has leading (light) and trailing (dark) edges. By increasing the width of the slit it was shown that a discharge peak in the histogram coincides with the passage of one or other of the two edges over a particular region (discharge centre) in the receptive field. Each edge has its own discharge centre which is fired when the edge has the correct orientation and direction of movement.3. The discharge centres in forty-three simple cell receptive fields were located by using one or more of the following stimuli for each cell:(i) slits of different width;(ii) single light and dark edges;(iii) a wide (3 degrees ) slit moved over a range of different velocities. The same locations were obtained when all three procedures were used on the same cell.4. Most cells (79%) discharged to both edges though not necessarily in the same direction of movement. The majority (72%) fired in only one direction and most commonly (51%) the cells responded to both edges in this one direction. In only 16% of cells did both types of edge excite in both directions of movement. When the one type of edge, light or dark, was considered, 84% of the cells were direction selective and, for these cells, the other edge fired only in the same direction (51%), in both directions (7%), only in the opposite direction (5%) or not at all (21%).5. Cells responding in one direction with a unimodal average response histogram may be responding to both edges, the two responses being concealed in the one discharge peak. The two discharge centres are then either nearly coincident or, more usually, slightly offset with respect to one another. Most commonly the dark edge centre is slightly in advance of the light edge centre.6. The discharge peaks in the bimodal and multimodal types come from discharge centres that are spatially separate, each centre firing to only one type of edge. In the case of the bimodal type the light edge centre always lies ahead of the dark edge centre.7. When a cell responds to a single edge in both directions of movement, the type of contrast effective in one direction is always the reverse of that in the other. When the cell responded in both directions, whether to one or both edges, most commonly a light edge discharge centre in one direction occupied approximately the same location in space as the dark edge centre in the reverse direction and vice versa for the other edge.8. Temporal aspects of the discharge of simple cells have been examined by recording the responses to moving slits and single edges over a wide range of velocities.

Mesh:

Year:  1971        PMID: 5157596      PMCID: PMC1331652          DOI: 10.1113/jphysiol.1971.sp009681

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  14 in total

1.  Residual eye movements in receptive-field studies of paralyzed cats.

Authors:  R W Rodieck; J D Pettigrew; P O Bishop; T Nikara
Journal:  Vision Res       Date:  1967-01       Impact factor: 1.886

2.  Binocular interaction fields of single units in the cat striate cortex.

Authors:  P O Bishop; G H Henry; C J Smith
Journal:  J Physiol       Date:  1971-07       Impact factor: 5.182

3.  Receptive fields and functional architecture of monkey striate cortex.

Authors:  D H Hubel; T N Wiesel
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

4.  Binocular single vision and depth discrimination. Receptive field disparities for central and peripheral vision and binocular interaction on peripheral single units in cat striate cortex.

Authors:  D E Joshua; P O Bishop
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

5.  Multiple projection of the visual field to the medical portion of the dorsal lateral geniculate nucleus and the adjacent nuclei of the thalamus of the cat.

Authors:  W J Kinston; M A Vadas; P O Bishop
Journal:  J Comp Neurol       Date:  1969-07       Impact factor: 3.215

6.  Responses to moving slits by single units in cat striate cortex.

Authors:  J D Pettigrew; T Nikara; P O Bishop
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

7.  Functional synaptic organization of primary visual cortex neurones in the cat.

Authors:  O Creutzfeldt; M Ito
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

8.  Analysis of receptive fields of cat retinal ganglion cells.

Authors:  R W Rodieck; J Stone
Journal:  J Neurophysiol       Date:  1965-09       Impact factor: 2.714

9.  Quantitative analysis of cat retinal ganglion cell response to visual stimuli.

Authors:  R W Rodieck
Journal:  Vision Res       Date:  1965-12       Impact factor: 1.886

10.  Postsynaptic potentials in the cat's visual cortex following electrical stimulation of afferent pathways.

Authors:  S Watanabe; M Konishi; O D Creutzfeldt
Journal:  Exp Brain Res       Date:  1966       Impact factor: 1.972

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  71 in total

1.  Responses of striate cortex cells to grating and checkerboard patterns.

Authors:  K K De Valois; R L De Valois; E W Yund
Journal:  J Physiol       Date:  1979-06       Impact factor: 5.182

2.  Responses of single units in the monkey superior colliculus to moving stimuli.

Authors:  J Moors; A J Vendrik
Journal:  Exp Brain Res       Date:  1979-04-02       Impact factor: 1.972

3.  The detection of gratings by independent activation of line detectors.

Authors:  P E King-Smith; J J Kulikowski
Journal:  J Physiol       Date:  1975-05       Impact factor: 5.182

4.  Periodic excitability changes across the receptive fields of complex cells in the striate and parastriate cortex of the cat.

Authors:  D A Pollen; S F Ronner
Journal:  J Physiol       Date:  1975-03       Impact factor: 5.182

5.  Response characteristics of the cells of cortical area 21a of the cat with special reference to orientation specificity.

Authors:  B M Wimborne; G H Henry
Journal:  J Physiol       Date:  1992-04       Impact factor: 5.182

6.  Shorter latencies for motion trajectories than for flashes in population responses of cat primary visual cortex.

Authors:  Dirk Jancke; Wolfram Erlhagen; Gregor Schöner; Hubert R Dinse
Journal:  J Physiol       Date:  2004-02-20       Impact factor: 5.182

7.  Correlations between directional and orientational tuning of cells in cat striate cortex.

Authors:  F Wörgötter; T Muche; U T Eysel
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

8.  A nonlinear model of the behavior of simple cells in visual cortex.

Authors:  Miguel A García-Pérez
Journal:  J Comput Neurosci       Date:  2004 Nov-Dec       Impact factor: 1.621

9.  A quantitative study of the projection area of the central and the paracentral visual field in area 17 of the cat. II. The spatial organization of the orientation domain.

Authors:  K Albus
Journal:  Exp Brain Res       Date:  1975-12-22       Impact factor: 1.972

10.  A dynamic nonlinearity and spatial phase specificity in macaque V1 neurons.

Authors:  Patrick E Williams; Robert M Shapley
Journal:  J Neurosci       Date:  2007-05-23       Impact factor: 6.167

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