Serum lipid fatty acids, phonological processing, and reading in children with oral clefts.

Reading skill is suggested to be related to phonological processing ability and polyunsaturated fatty acids (PUFAs). Here we investigated whether fatty acids (FAs) are related to phonological processing, whether the relations between PUFAs and reading generalize to other FAs, whether these relations are mediated by phonological processing, and whether relations of FAs are specific for language-related functions. Blood samples of 49 ten-year-old children with oral clefts were collected for FA proportion analysis in serum cholesteryl esters and phospholipids. On the same day, they performed tasks of phonological processing, reading, and both verbal and nonverbal intelligence. Sequential regression analyses (adjusted for age, gender, and cleft type) showed that phonological processing was inversely related to myristic acid in phospholipids and positively related to eicosapentaenoic acid in cholesteryl esters. Reading was inversely related to palmitoleic and gammalinolenic acids in phospholipids. The relations between FAs and reading were not mediated by phonological processing and FAs related only to language-related functions.

Serum lipid fatty acids and temporal processing acuity in children with oral clefts.

We investigated the relation between a biological factor (fatty acids, FA) and a cognitive processing speed factor (temporal processing acuity, TPA) that are both suggested to relate to neuronal and cognitive functioning. Blood samples of 49 ten-year-old children with oral clefts were collected for FA analysis in serum triglycerides, cholesteryl esters, and phospholipids on the same day as they performed behavioral TPA tasks (simultaneity/nonsimultaneity judgments) in several perceptual modalities (visual, auditory, tactile, audiotactile, visuotactile, and audiovisual). This population has larger than expected variation in the relevant cognitive measures (TPA, learning ability, and intelligence). Sequential regression analyses (adjusted for age, gender, and cleft type) showed that saturated FAs were not generally associated with TPA. Monounsaturated erucic and nervonic acids were inversely related with TPA. Of the polyunsaturated fatty acids, eicosapentaenoic and docosahexaenoic acids were positively associated with TPA, whereas gamma-linolenic acid was inversely related to TPA. In summary, we found significant relations between a biological (certain FAs) and a cognitive factor (TPA).

Mu rhythm modulation during changes of visual percepts.

Cooperation between vision and somatomotor behavior, such as manual exploration of objects, suggests close functional coupling between the visual and sensorimotor systems. We observed this type of interaction in human volunteers during binocular rivalry while following the level of sensorimotor mu rhythm with a whole-scalp neuromagnetometer. The observers viewed a weak vertical grating in the lower visual field of one eye and a strong horizontal grating in the same spatial window of the other eye. When stationary, the weak grating was permanently invisible because of its low contrast and spatial frequency. A sudden brief drifting movement of the weak grating wiped out the dominant grating, and the weak grating became visible for less than the 3-s interval between the movements. The postcentral 8- to 15-Hz mu rhythm was found in six of nine observers, and its level increased transiently by 10-15%, starting about 450 ms after the beginning of the movement. The mu level was also enhanced by the actual disappearance of the stronger stimulus, when it occurred in random order with the rivalry stimuli. Identical visual motion, when not accompanied by a perceptual dominance change, produced only minor effects on the mu rhythm. Our results show that a change in visual percept, even with no real or imagined motor response, is associated with modified activity of the postcentral gyrus. This modification may reflect visuohaptic interactions and/or activity of the distributed cortical network implementing visually guided movements.

Analysis of spatial structure in eccentric vision.

The analysis of spatial structure, ie, the encoding of relative positions between pattern elements, was studied in central and eccentric vision. In a two-alternative forced-choice task the observer had to discriminate between two patterns consisting of short line segments. At each trial the two patterns were flashed for 140 msec and the observer indicated whether the patterns were identical or mirror symmetric. Psychometric functions were measured by changing pattern size at each eccentricity in order to find the threshold size allowing 75% of correct responses. The scaling factor, required for discriminating between mirror symmetric and identical patterns independent of eccentricity, was found to be similar to the size-scaling proposed by Levi et al (Vision Res 25:963, 1985) for vernier acuity tasks.

Resolution of gratings oriented along and across meridians in peripheral vision.

Grating resolution was measured at various locations of the visual field for four grating orientations. As an instance of the oblique effect, vertical and horizontal gratings produced the highest resolution values in the central area. At eccentricities larger than about 20 deg, the oblique effect was replaced by a meridional resolution effect, in which resolution was systematically best for meridionally oriented grating bars and worst for grating bars perpendicular to the visual-field meridians. The origin of the effect seems to be neural because it was not caused by peripheral refractive errors or optical distortion of the peripheral retinal image.

Cortical magnification, scale invariance and visual ecology.

The visual world of an organism can be idealized as a sphere. Locomotion towards the pole causes translation of retinal images that is proportional to the sine of eccentricity of each object. In order to estimate the human striate cortical magnification factor M, we assumed that the cortical translations, caused by retinal translations due to the locomotion, were independent of eccentricity. This estimate of M agrees with previous data on magnifications, visual thresholds and acuities across the visual field. It also results in scale invariance in which the resolution of objects anywhere in the visual field outside the fixated point is about the same for any viewing distance. Locomotion seems to be a possible determinant in the evolution of the visual system and the brain.

Illusory perception of gratings stimulating a small number of neurones.

We studied pattern perceptions caused by drifting gratings presented monocularly in the nasal and temporal visual fields at various suprathreshold contrasts. The grating and its surround and background were matched in luminance. Small grating produced illusions and reduced perceptions. When grating area or contrast increased from a subthreshold value, the gratings were first seen as mere flashes. Then each grating was sometimes perceived as a single small bright spot or point. Next each grating was seen as a single dark or bright line. Finally the stimuli were perceived as gratings consisting of several bars. Orientation or direction of movement were perceived correctly, but velocity, colour and number of bars were often perceived as illusions. Thus, in spite of the illusions, some features of the stimuli could have allowed correct discriminations. The area and contrast limits of illusory perception depended on eccentricity. Irrespective of retinal size, the stimuli were not perceived correctly as gratings at any eccentricities when the gratings were smaller than about 1 x 1 mm in their calculated cortical area and stimulated a small constant number of retinal ganglion cells. Relations between the results and retinal aliasing, cortical columns and phase locking of neuronal oscillations are discussed.

Temporal contrast sensitivity and cortical magnification.

We measured temporal and spatial contrast sensitivity functions of foveal and peripheral photopic vision at various locations in the nasal visual field. Sensitivity decreased monotonically with increasing eccentricity when it was measured by using the same test gratings at different eccentricities. When the gratings were normalized in area, spatial frequency, and translation velocity by means of the cortical magnification factor M so that the calculated cortical representations of the gratings became equivalent at different eccentricities, the temporal contrast sensitivity functions became similar at all eccentricities. The normalization was effective under all experimental conditions that included various kinds of temporal modulation from 0 to 25 Hz (movement, counterphase flicker and on-off flicker) and different threshold tasks (detection, orientation discrimination, and discrimination of movement direction), independently of the subjective appearances of the gratings at threshold. We conclude that central and peripheral vision are qualitatively similar in spatiotemporal visual performance. The quantitative differences observed without normalization seem to be caused by the spatial sampling properties of retinal ganglion cells that are directly related to the values of M used in the normalization.

Mesopic spectral responses and the Purkinje shift of macaque lateral geniculate nucleus cells.

Spectral responsiveness of different classes of macaque LGN cells at eccentricities smaller than 12 degrees was studied at low light intensities. Cone thresholds of cells varied from 1 to 10 td. Rod inputs were found in all classes of cells, including inhibitory inputs in some cells. Rod inputs were not apparent above 10-40 td, giving a total mesopic range of about 1-40 td. Strong rod-mediated responses could be evoked in broadband phasic cells and in spectrally opponent cells excited by short wavelengths. Only weak if any excitatory responses could be evoked by short wavelengths at scotopic levels in spectrally opponent long-wavelength excited cells. Hence, rod inputs do not confound the spectral responsiveness of cells because no spectrally opponent cell excited by long-wavelength stimuli at photopic levels became significantly responsive to short wavelength stimuli at mesopic or scotopic intensities. The so-called "rod color" may be blue. An increase in the dominance of wide-band cell responses that may explain the Bezold-Brücke hue shift was observed at higher stimulus radiances at wavelengths near 450 and 650 nm.

Rate of information segregation in developmentally dyslexic children.

Slowed processing of sequential perceptual information is related to developmental dyslexia. We investigated this unimodally and crossmodally in developmentally dyslexic children and controls ages 8-12 years. The participants judged whether two spatially separate trains of brief stimuli, presented at various stimulus onset asynchronies (SOA) in one or two senses, were synchronous or not. The stimulus trains consisted of light flashes in vision, clicks in audition, and indentations of the skin in the tactile sense. The dyslexic readers required longer SOAs than controls for successful performance in all six comparisons. The crossmodal spatiotemporal resolution of the groups differed more than unimodal performance. The dyslexic readers' segregation performance was also less differentiated than that of the controls. Our results show that not only sensory but also polysensory nonverbal information processing is temporally impaired in dyslexic children.

[Inhibition and space-frequency characteristics of the complex receptive fields of the cat visual cortex]. / Tormozhenie i prostranstvenno-chastotnye kharackteristiki slozhnykh retseptivnykh polei zritel'noi kory koshki.

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.

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.

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.

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.

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.