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Biomedical subjects

V Virsu

Publications and source records attributed to V Virsu.

17 recordsLinked to original sources
PubMed1979

Visual resolution, contrast sensitivity, and the cortical magnification factor.

This study shows that photopic contrast sensitivity and resolution can be predicted by means of simple functions derived by using the cortical magnification factor M as a scale factor of mapping from the visual field into the striate cortex. We measured the minimum contrast required for discriminating the direction of movement or orientation of sinusoidal gratings, or for detecting them in central and peripheral vision. No qualitative differences were found between central and peripheral vision, and almost all quantitative differences observed could be removed by means of a size compensation derived from M. The results indicated specifically that (1) visual patterns can be made equally visible if they are scaled so that their calculated cortical representations become equivalent; (2) contrast sensitivity follows the same power function of the cortical area stimulated by a grating at any eccentricity; (3) area and squared spatial frequency are reciprocally related as determinants of contrast sensitivity; and (4) acuity and resolution are directly proportional to M, and the minimum angle of resolution is directly proportional to M-1. The power law of spatial summation expressed in (2) and (3) suggests the existence of a central integrator that pools the activity of cortical neurons. This summation mechanism makes the number of potentially activated visual cells the most important determinant of visibility and contrast sensitivity. The functional homogeneity of image processing across the visual field observed here agrees with the assumed anatomical and physiological uniformity of the visual cortex.

Brain Mapping↗
PubMed1979

An estimation and application of the human cortical magnification factor.

Comparisons of the published data on the density D of receptive fields of retinal ganglion cells and on the cortical magnification factor M indicated that M2 is directly proportional to D in primates. Therefore, the human M can be estimated for the principal meridians of the visual field from the density-distribution of retinal ganglion cells and from the density of the centralmost cones. Using the previously published empirical data, we estimated the values of the human M and express the values in four simple equations that can be used for finding the value of M for any location of the visual field. The monocular values of M are not radially symmetric. These analytically expressed values of M make it possible to predict contrast sensitivity and resolution for any location of the visual field. We measured contrast sensitivity functions at 25 different locations and found that the functions could be made similar by scaling the retinal dimensions of test gratings by the inverse values of M. Visual acuity and resolution could be predicted accurately for all retinal locations by means of a single constant multiplier of the estimated M. The results indicate that the functional and structural properties of the visual system are very closely and similarly related across the whole retina. Visual acuity, e.g., bears the same optimal relation to the density of sampling executed by retinal ganglion cells at all locations of the visual fields.

Brain Mapping↗
PubMed1979

[Inhibition and space-frequency characteristics of the complex receptive fields of the cat visual cortex].

Responses of complex receptive fields of the cat straitum to moving sinusoidal grating were studied. Stimulation of the receptive field with some spatial frequencies suppresses spontaneous discharges. Responses of the receptive field corroborate previously made predictions that the spatial--frequency characteristics of the receptive field should have the main and the secondary maximums and negative areas in case the complex fields perform piece-wise Fourier--transformation of image. The changes of impulse frequency in field's response are predicted by comparing the changes of instantaneous spectrum of grating entering the field with spatial frequency characteristic of the field. The data evidence that the complex field is rather a spatial--frequency filter than a detector. Some complex fields reveal a lateral inhibitory area behind the field's nucleus in direction of stimulus movement. The complex fields with no lateral inhibitory areas seem to serve for piece Fourier--description of image, those with lateral areas--for picking out the countour between textures.

Animals↗
PubMed1978

Retinal mechanisms of visual adaptation and afterimages.

Recent results obtained from recordings of isolated photoreceptor activity and from correlations of this activity with time-dependent changes in the responses of other retinal cells in several vertebrates have made a thorough revision of former theories of visual adaptation necessary. The present paper reviews the current state of research and relates the new discoveries with psychophysical findings in an attempt to explain human light and dark adaptation from the novel starting point. The former conceptions of adaptation have to be replaced with a three-level process consisting of photochemical receptor neural and network adaptation. Several adaptive mechanisms can be discerned at each level. Depending on adaptation conditions, any level of the three can play a dominating role and can also produce afterimages that display the behaviour of the mechanisms working at each level. The total achievement of visual adaptation is an optimized end product of the actions of all the various mechanisms.

Adaptation, Ocular↗
PubMed1977

Dark adaptation and receptive field organisation of cells in the cat lateral geniculate nucleus.

The receptive fields of LGN cells were investigated with stationary light and dark spot and annulus stimuli. Stimulus size and background intensity were varied while stimulus/background contrast was kept constant. The speed of dark adaptation vaired considerably from cell to cell. Dark adaptation made responses more sustained in all neurones and eliminated the oscillatory on-responses evoked under some conditions in the light-adapted cells. Dark adaptation led also to a disappearance of early phasic inhibition in on-responses, and increased response rise time and latency. The power of surround responses to inhibit centre responses decreased slightly at low levels of light adaptation in LGN cells but much less than in retinal ganglion cells. Some other traces of changing retinal surround effects also appeared inthe LGN on dark adaptation. For example, the functional size of receptive fields increased at low levels of illuminance as has been observed in retinal ganglion cells and the receptive fields as estimated from response peaks were larger than those estimated from sustained components.

Animals↗
PubMed1977

Responses of cells in the cat lateral geniculate nucleus to moving stimuli at various levels of light and dark adaptation.

The responses of neurones in laminae A and A1 of the cat lateral geniculate nucleus to moving stimuli were investigated at different background luminances. Moving bright slits, dark bars and edges were employed; the contrast of stimuli against the background was held constant. Background intensities varied from 10(-3) to 10(2) td. Responses as stimuli passed across the centres of LGN receptive fields became stronger with increasing levels of light adaptation up to 10(-1)-10(1) td and then remained constant. Responses as stimuli passed through surround regions altered qualitatively with adaptation level, generally increasing in strength and complexity with background luminance. As a bright slit for on-centre cells or dark bar for off-centre cells left the surround, in almost all units a strong secondary peak could be elicited by an appropriate selection of the adaptation conditions. Many features of the responses to moving stimuli could not be predicted from the responses to stationary stimuli under different adaptation conditions described in the previous paper.

Animals↗
PubMed1977

Psycholphysical 'measurement' of cortical colour mechanisms: reply of Meyer.

In a paper recently published in this journal, Meyer criticised our study on relationships between channels for colour and spatial frequence for not being able to demonstrate a size aftereffect not specific to colour, a McCollough effect not specific to size, or the functions of cortical colour mechanisms. In fact, our study attempted none of these demonstrations in the sense suggested by Meyer because the first would have been impossible for empirical reasons, the second for conceptual reasons, and the third for methodological reasons. Instead, our study yielded evidence that at least three different types of perceptual channel underlie our capacity to perceive the size and colour of objects.

Afterimage↗
PubMed1975

Central inhibitory interactions in human vision.

Contrast threshold and perceived orientation of a line segment were measured when another line segment was simultaneously presented either to the same or the other eye; the angle between the two line segments was varied. The presence of the masking line elevated the contrast threshold under both conditions and the threshold increased similarly both in monoptic and dichoptic masking when the masking angle was made smaller. The presence of the masking line affected also the perceived orientation of the test line. The effect was similar both in monoptic and dichoptic masking; the largest change of perceived orientation occurred at about 15 degrees masking angle and the change was smaller at other angles. The effect disappeared within a short distance when the masking line was removed farther from the test line. The similarity of the monoptic and dichoptic threshold elevations demonstrates that there are lateral inhibitory interactions between central neural units in the human visual system. It is likely that the interacting units mediate the perception of contour orientation, for the threshold elevation functions were consistent with concurrent changes of perceived orientation. The results are evidence for the hypothesis that inhibition between orientation detectors is a factor in the perceptual expansion of acute angles.

Humans↗
PubMed1975

Human auditory evoked responses during hangover.

Auditory evoked responses (AER) to trains of 6 click stimuli (1 click/sec) were studied in 9 subjects under hangover, tired control, and normal control conditions in order to find out whether the symptoms of hyperexcitability during hangover have a correlate in the characteristics of the AER. In addition, the audiograms were measured. AERs to the first click in a stimulus train were markedly smaller during hangover than in the other 2 states. The amplitude levels of the AERs during the repetition of the click stimulus were, however, similar under all three conditions. The audiograms obtained in the three states were similar except for a very slight decrease of auditory threshold sensitivity during hangover as compared with the tired control condition. The results show that the effects of hangover on AERs resemble those of alcohol intoxication. The symptoms of hyperexcitability during hangover cannot be explained in terms of increased peripheral sensitivity.

Acoustic Stimulation↗
PubMed1975

Dark adaptation and short-wavelength backgrounds decrease perceived size.

The effects of background luminance, contrast, and background wavelength on the perceived size of small line figures were studied at mesopic levels of light adaptation. Perceived size diminished at low levels of background luminance. The effect disappeared at high levels of luminance. Perceived size of luminous circles increased as a logarithmic function of background luminance when the background intensity did not exceed 25 td(1). The strength of the size effect decreased as a function of circle diameter from 0-125 to 2 deg of visual angle(2). Perceived size of small luminous circles, subtending less than 0-5 deg, also increased as a function of contrast at low values of contrast but at very high values of contrast there was a decrease in perceived size. Background luminance had the same effect on the perceived size of circles as on the perceived size of spatial cycles in gratings. Control experiments led to the conclusion that dark adaptation is the primary source of the size effects. The main evidence for this conclusion was obtained from a demonstration that the same background luminance produced either an increase or a decrease in perceived size, depending on the adaptational state of the eye. It was also found that a shift from cone vision to rod vision contributes to the effects, for a stimulus looked smaller on a short-wavelength background than on a long-wavelength background. The size effects can be predicted from the changes of receptive-field properties of single neurones under corresponding conditions of stimulation, if it is assumed that the perception of size is mediated by size-specific channels formed of single neurones. Stimulation that leads to an activation of small receptive fields appears to indicate to the brain the presence of small retinal images. If small receptive fields are experimentally made responsive to larger retinal images, an underestimation of size results.

Dark Adaptation↗