Spatio‐temporal interaction in neurones of the cat's dorsal lateral geniculate nucleus.

Temporal contrast sensitivities in the range 0.33‐42 Hz for optimum spatial frequency grating stimuli were measured for large populations of XG and YG neurones. For fewer cells, complete spatial contrast sensitivity profiles were measured at a series of temporal frequencies and, in some cases, at a range of levels of retinal illumination too. Contrast sensitivities were measured from responses of cells reliably different from their maintained discharges. The cells’ discharges were recorded extracellularly from the binocular segment of the A laminae of the cat's dorsal lateral geniculate nucleus. At their respective optimum spatial frequencies, YG cell were more sensitive on average than XG cells for most temporal frequencies, though the average temporal contrast sensitivity profiles of both cell classes had similar shapes. The optimum temporal frequency for both cell types was around 5 Hz. XG and YG cells seem to be relatively less sensitive to low temporal frequencies than their ganglion cell counterparts. At a retinal illumination of 230 cd/m2 (pupil, 3 mm2), increasing temporal frequency in the range 0.65‐21 Hz produced a relative improvement in low spatial frequency contrast sensitivity in most XG and all YG cells studied. There were some XG cells, though, which showed little or no effect of temporal frequency on their spatial contrast sensitivity curves. At all temporal frequencies, the shapes of spatial contrast sensitivity curves and the cells’ temporal contrast sensitivity profiles were not markedly dependent on the criterion level set to measure ‘threshold’ contrast. Reducing the level of retinal illumination in the range 230‐0.007 cd/m2 (pupil, 3 mm2) produced a fall in contrast sensitivities for both XG and YG cells. The loss in sensitivity was more marked at high spatial and high temporal frequencies. The similar shapes of the temporal contrast sensitivity curves of XG and YG cells weakens the suggestion that the human counterparts of these cells would provide a suitable physiological substrate for the psychophysical sustained and transient channels. Although the behaviour of XG and YG cells parallels quite closely changes in cat and human psychophysical spatial contrast sensitivities with temporal frequency and retinal illumination, many problems remain for equating results from the two fields.

[1]  C. Enroth-Cugell,et al.  Spatio‐temporal interactions in cat retinal ganglion cells showing linear spatial summation. , 1983, The Journal of physiology.

[2]  J. Movshon,et al.  Spatial and temporal contrast sensitivity of striate cortical neurones , 1975, Nature.

[3]  R. Shapley,et al.  Receptive field mechanisms of cat X and Y retinal ganglion cells , 1979, The Journal of general physiology.

[4]  P. Lennie,et al.  The influence of temporal frequency and adaptation level on receptive field organization of retinal ganglion cells in cat , 1982, The Journal of physiology.

[5]  C. Enroth-Cugell,et al.  Adaptation and dynamics of cat retinal ganglion cells , 1973, The Journal of physiology.

[6]  William H. Merigan,et al.  The luminance dependence of spatial vision in the cat , 1981, Vision Research.

[7]  S. Sherman,et al.  Spatial and temporal sensitivity of X- and Y-cells in dorsal lateral geniculate nucleus of the cat. , 1980, Journal of neurophysiology.

[8]  J. Troy Spatial contrast sensitivities of X and Y type neurones in the cat's dorsal lateral geniculate nucleus. , 1983, The Journal of physiology.

[9]  C. Enroth-Cugell,et al.  The contrast sensitivity of retinal ganglion cells of the cat , 1966, The Journal of physiology.

[10]  D. Tolhurst Separate channels for the analysis of the shape and the movement of a moving visual stimulus , 1973, The Journal of physiology.

[11]  H. Barlow,et al.  MAINTAINED ACTIVITY IN THE CAT'S RETINA IN LIGHT AND DARKNESS , 1957, The Journal of general physiology.

[12]  E Kaplan,et al.  Effects of dark adaptation on spatial and temporal properties of receptive fields in cat lateral geniculate nucleus. , 1979, The Journal of physiology.

[13]  P Lennie,et al.  The control of retinal ganglion cell discharge by receptive field surrounds. , 1975, The Journal of physiology.

[14]  R. Shapley,et al.  The effect of contrast on the transfer properties of cat retinal ganglion cells. , 1978, The Journal of physiology.

[15]  Lawrence E. Arend,et al.  Temporal determinants of the form of the spatial contrast threshold MTF , 1976, Vision Research.

[16]  J. Robson Spatial and Temporal Contrast-Sensitivity Functions of the Visual System , 1966 .

[17]  J. Bergen,et al.  A four mechanism model for threshold spatial vision , 1979, Vision Research.

[18]  O. Grüsser,et al.  Temporal Transfer Properties of the Afferent Visual System Psychophysical,Neurophysiological and Theoretical Investigations , 1973 .

[19]  P Lennie,et al.  Perceptual signs of parallel pathways. , 1980, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.