The aims of this study were to identify the locations of areas in the human cortex responsible for describing fragmented test images of different degrees of ordering and to identify the areas taking decisions regarding stimuli of this type. The locations of higher visual functions were determined by functional magnetic resonance imaging (fMRI) using a scanner fitted with a superconducting magnet and a field strength of 1.5 T. The blood oxygen level-dependent (BOLD) method was based on measurements of the level of hemoglobin oxygenation in the blood supplied to the brain. This level was taken to be proportional to the extent of neuron activation in the corresponding part of the gray matter. Stimuli were matrixes consisting of Gabor elements of different orientations. The measure of matrix ordering was the ratio of the number of Gabor elements with identical orientations to the total number of elements in the image. Brain neurons were activated by simultaneous changes in the orientations of all the elements, leading to substitution of one matrix by another. Substitution of the orientation was perceived by observers as rotation of the elements in the matrix. Stimulation by matrixes with a high level of ordering was found to activate the occipital areas of the cortex, V1 and V2 (BA17-BA18), while presentation of matrixes with random element orientations also activated the parietal-temporal cortex, V3, V4, V5 (BA19), and the parietal area (BA7). Brain zones responsible for taking decisions regarding the level of order or chaos in the organization of the stimuli are located in different but close areas of the prefrontal and frontal cortex of the brain, including BA6, BA9, and BA10. The results are assessed in terms of concepts of the roles and interactions of different areas of the human brain during recognition of fragmented images of different degrees of complexity.

Electrophysiological studies were performed to measure the threshold (upper end of range) spatial frequency using visual evoked potentials and comparison with visual acuity neuron 26 healthy subjects. The aim of the present work was to create a method for objective measurement of visual acuity. This was addressed by initial measurements using a universally accepted method of visual stimulation and processing of electroencephalograms, which allows errors due to individual differences in visual system function to be minimized. These experiments yielded a strong correlation between the threshold spatial frequency of the test grid yielding an evoked potential on presentation and visual acuity, in degrees, expressed as the resolving ability of the visual system for this optotype. A logarithmic relationship was found between these values and an equation allowing automated calculation of visual acuity (resolving ability) from electrophysiological data was derived. The results were independent of the subject's responses and therefore provides a maximally objective assessment of visual acuity.

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The aim of the present work was to study the interaction between the optical properties of images of " disappearing" optotypes and their recognition thresholds. The "disappearing" optotypes were figures with complex outlines and had a unique property - they were close to the threshold of recognition and observation, which increases the accuracy of measurement of visual acuity and the subjects' attention to them. The recognition distances of "disappearing" optotypes were measured. A relationship was found between the recognition distance of "disappearing" optotypes and different optical density profiles on the one hand and the spatial and spatial frequency characteristics of the stimuli on the other. The decisive factor determining the threshold of recognition of optotypes in spatial frequency terms is its spatial frequency spectrum; that in spatial terms is the width of the black/white pair or black-white triad in the complex outline. Regardless of the shape of the optotype, one of the most important limiting factors was the concordance of this test with the scattering function of the subject's eye optics.

10. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.