Literature DB >> 7411174

Extrageniculostriate vision in the monkey. VII. Contrast sensitivity functions.

M Miller, P Pasik, T Pasik.   

Abstract

1. Psychophysical and electrophysiological experiments have indicated the importance of spatial frequency components and their respective contrasts and orientations for the recognition of patterns. It is in the striate cortex where these types of information first converge, a fact that lends support to the accepted crucial role of this structure in pattern discrimination. 2. Monkeys with total bilateral ablation of the striate cortex, however, retain a residual capacity for pattern discrimination and also can differentiate between a vertical and an oblique luminous bar. The present study explores their capacity for spatial frequency detection both as a function of contrast and, by extrapolation, at maximum contrast (visual acuity measure). 3. Monkeys were presented with a forced choice between a homogeneous target and a vertically oriented sinusoidal grating in a pulling-in apparatus. Stimuli were produced by the transillumination of transparencies at spatial frequencies of 0.5, 1.0, 2.0, 4.0, 8.0, 16, and 32 cycles/deg, in 0.1-log unit steps of contrast from 0.79 to 0.006. The stimuli subtended 8 degrees of visual angle and were matched for mean luminance at 20 cd/m2. After mastering the discrimination of one spatial frequency at the highest contrast, contrast thresholds were first estimated by a staircase technique, and then determined by the method of constant stimuli. The procedure was repeated for each spatial frequency before and after histologically verified total bilateral removal of striate cortex and partial damage to circumstriate cortices. 4. Discrimination at all spatial frequencies was mastered by all normal monkeys. Postoperatively, they could solve only problems with frequencies between 0.5 and 4.0 cycles/deg. 5. Contrast sensitivity (threshold-1) functions for normal and destriated monkeys have the characteristic inverted J shape. The high- and low-frequency limbs are related exponentially to spatial frequency, and the peak of the curve is about 2.0 cycles/deg. The dimensions of the functions, however, change significantly following the ablation. Sensitivity is depressed at all spatial frequencies. The mean "visuogram" indicates a 26-dB flat loss. 6. The mean high-frequency cutoff point is 43 cycle/deg preoperatively and 12 cycles/deg postoperatively, equivalent to 0.7' and 2.5' of arc, respectively. The latter value is not worse than 20/80 on the Snellen chart. 7. The variability of the response at each spatial frequency in the staircase method and the slope of the psychometric function derived from the method of constant stimuli provide a measure of "instability" and "precision," respectively, which are inversely related. Preoperatively, precision is significantly greater at high than at low spatial frequencies. Postoperatively, it is similar at all frequencies, and the values are lower than those determined preoperatively. 8. The results demonstrate that destriated monkeys can detect gratings, although to a lesser degree than normal animals...

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Year:  1980        PMID: 7411174     DOI: 10.1152/jn.1980.43.6.1510

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  11 in total

Review 1.  Developmental physiological optics and visual acuity: a brief review.

Authors:  J V Odom; M Green
Journal:  Experientia       Date:  1984-11-15

2.  Extrageniculostriate vision in the monkey. VIII. Critical structures for spatial localization.

Authors:  S J Solomon; T Pasik; P Pasik
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

3.  Alterations of retinal inputs following striate cortex removal in adult monkey.

Authors:  J Dineen; A Hendrickson; E G Keating
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

Review 4.  Primary visual cortex: awareness and blindsight.

Authors:  David A Leopold
Journal:  Annu Rev Neurosci       Date:  2012       Impact factor: 12.449

5.  Amygdala engagement in response to subthreshold presentations of anxious face stimuli in adults with autism spectrum disorders: preliminary insights.

Authors:  Geoffrey B C Hall; Krissy A R Doyle; Jeremy Goldberg; Dianne West; Peter Szatmari
Journal:  PLoS One       Date:  2010-05-25       Impact factor: 3.240

6.  Visual evoked potentials in acute occipital blindness. Diagnostic and prognostic value.

Authors:  C W Hess; O Meienberg; H P Ludin
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

7.  Central and peripheral residual vision in humans with bilateral deprivation amblyopia.

Authors:  L Mioche; M T Perenin
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

Review 8.  The effect of glaucoma on central visual function.

Authors:  R L Stamper
Journal:  Trans Am Ophthalmol Soc       Date:  1984

Review 9.  Invariant visual object recognition and shape processing in rats.

Authors:  Davide Zoccolan
Journal:  Behav Brain Res       Date:  2015-01-02       Impact factor: 3.332

Review 10.  Fast Detector/First Responder: Interactions between the Superior Colliculus-Pulvinar Pathway and Stimuli Relevant to Primates.

Authors:  Sandra C Soares; Rafael S Maior; Lynne A Isbell; Carlos Tomaz; Hisao Nishijo
Journal:  Front Neurosci       Date:  2017-02-17       Impact factor: 4.677

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