Visual Processing Areas Research Articles

Sex Differences in Neural Mechanisms Underlying Implicit Symmetry Processing

Some species, including humans, prefer symmetrical to asymmetrical patterns. Preferences for symmetrical stimuli could have arisen in both sexes because specialized systems developed to detect and identify symmetrical stimuli, which are more likely to be figure than background. Females, it has been suggested, prefer symmetry because it may provide a cue to biological fitness when choosing a mate. Using functional magnetic resonance imaging, we found sex differences in neural activity when subjects distinguished figure from ground in abstract patterns whose component shapes differed in colour, brightness, and symmetry/asymmetry. Although no participant explicitly reported using symmetry as a decision criterion, women showed more neural activity than men in visual processing areas when the display contained a symmetrical shape. This enhanced activity in occipital cortex (middle and superior occipital gyrus) occurred bilaterally in women irrespective of whether they chose the symmetrical element in the display as the figure. Contrariwise, men showed a significant neural response in right temporal (superior temporal gyrus) and left parietal cortex (inferior parietal cortex/temporo-parietal junction) only when they chose a symmetrical element as the figure. The female brain thus appears to register symmetry automatically as a stimulus attribute, while the differential neurophysiological response of the male brain is dependent upon an explicit behavioural response to symmetry (choosing the symmetrical part of the display as figure), even if the criterion for choice (symmetry) is not reported verbally.

Neural basis of stereotype-induced shifts in women's mental rotation performance.

Recent negative focus on women's academic abilities has fueled disputes over gender disparities in the sciences. The controversy derives, in part, from women's relatively poorer performance in aptitude tests, many of which require skills of spatial reasoning. We used functional magnetic imaging to examine the neural structure underlying shifts in women's performance of a spatial reasoning task induced by positive and negative stereotypes. Three groups of participants performed a task involving imagined rotations of the self. Prior to scanning, the positive stereotype group was exposed to a false but plausible stereotype of women's superior perspective-taking abilities; the negative stereotype group was exposed to the pervasive stereotype that men outperform women on spatial tasks; and the control group received neutral information. The significantly poorer performance we found in the negative stereotype group corresponded to increased activation in brain regions associated with increased emotional load. In contrast, the significantly improved performance we found in the positive stereotype group was associated with increased activation in visual processing areas and, to a lesser degree, complex working memory processes. These findings suggest that stereotype messages affect the brain selectively, with positive messages producing relatively more efficient neural strategies than negative messages.

Linking retinotopic fMRI mapping and anatomical probability maps of human occipital areas V1 and V2

Using functional MRI, we characterized field sign maps of the occipital cortex and created three-dimensional maps of these areas. By averaging the individual maps into group maps, probability maps of functionally defined V1 or V2 were determined and compared to anatomical probability maps of Brodmann areas BA17 and BA18 derived from cytoarchitectonic analysis (Amunts, K., Malikovic, A., Mohlberg, H., Schormann, T., Zilles, K., 2000. Brodmann's areas 17 and 18 brought into stereotaxic space—where and how variable? NeuroImage 11, 66–84). Comparison of areas BA17/V1 and BA18/V2 revealed good agreement of the anatomical and functional probability maps. Taking into account that our functional stimulation (due to constraints of the visual angle of stimulation achievable in the MR scanner) only identified parts of V1 and V2, for statistical evaluation of the spatial correlation of V1 and BA17, or V2 and BA18, respectively, the a priori measure κ was calculated testing the hypothesis that a region can only be part of functionally defined V1 or V2 if it is also in anatomically defined BA17 or BA18, respectively. κ = 1 means the hypothesis is fully true, κ = 0 means functionally and anatomically defined visual areas are independent. When applying this measure to the probability maps, κ was equal to 0.84 for both V1/BA17 and V2/BA18. The data thus show a good correspondence of functionally and anatomically derived segregations of early visual processing areas and serve as a basis for employing anatomical probability maps of V1 and V2 in group analyses to characterize functional activations of early visual processing areas.

An fMRI study of the differential effects of word presentation rates (reading acceleration) on dyslexic readers' brain activity patterns

Several lines of evidence have recently provided a clear indication that word reading rate can be considered as an independent variable which influences comprehension as well as accuracy in reading. Thus, not only is fluent reading a critical characteristic of skilled (automatic) reading, it has been shown that faster reading does not necessarily incur a cost in terms of accuracy. Indeed, readers of various levels of reading proficiency, as well as clearly impaired readers (dyslexics), if made to read faster than their normal (routine) reading rate, can increase their decoding accuracy and comprehension. Using block design, blood-(de)oxygenation-level-dependent (BOLD) functional magnetic resonance imaging we studied the differences in brain activation patterns induced by reading and script processing in adult dyslexics and normal reading controls as a function of two word presentation rates. Word presentation rates were set individually for each participant to correspond to his/her routine reading rate (slow) and to a correspondingly faster rate (fast). Three task conditions were tested: sentences (plausibility judgment), single words (concrete/abstract judgment), non-words (homophonic judgment). Comprehension and accuracy in the faster presentation rates were unimpaired in both groups. There were no significant differences between the activation patterns induced in both groups in ‘slow’ reading of sentences and single words, but ‘fast’ reading was related to higher activations in visual areas in the normal readers. However, in the slow non-words condition the dyslexics were characterized by activations in the Lt IFG (Broca's area) and operculum, while the control readers clearly activated visual processing areas (extra-striate cortex). These differences in brain activation patterns were not found in the fast non-words condition. We propose that time-constrained (accelerated) script decoding may prompt the dyslexic brain to process graphemic information in a different manner compared to the one employed in unconstrained (routine) reading, in some conditions in a manner of processing much closer to the one employed by normal reading controls.

Regional Brain Activity Associated with Visual Backward Masking

In visual backward masking, the visibility of a briefly presented visual target is disrupted by a mask that is presented shortly thereafter. The goal of the current study was to identify regions in the human cortex that may provide the neural basis of visual masking. We searched for areas whose activity correlated with perception as we systematically varied the strength of masking. A total of 13 subjects performed a backward masking task during functional magnetic resonance imaging. Target and mask were presented at three delay intervals (34, 68, and 102 msec) and behavioral measures confirmed that the targets were more visible at longer masking intervals. Two sets of regions of interest were identified: Distinct regions in the visual cortex (V1/V2, LO, hMT+) were segregated using scans to localize visual processing drawn from the existing literature. Additional cortical regions were selected in a data-driven approach based on their activity during the backward masking task. For each set, we determined the regions whose magnitude of activation increased at longer masking intervals. Nine of the subjects provided valid behavioral performance data on the visual masking task and imaging data from these subjects were used for subsequent analysis. The scans of visual processing areas identified four regions, including: early visual areas (V1 and V2), the motion-sensitive regions in the lateral occipital (LO) lobe (hMT+), and two components (dorsal and ventral) of the object-sensitive region, LO. Of these, the ventral and dorsal LO regions were sensitive to the strength of the mask. For the data-driven approach, six regions were identified on the basis of a difference map in which all masking intervals were contrasted with rest. These included the inferior parietal, anterior cingulate, precentral, insula, thalamic, and occipital areas. The predicted effects of more activity with weaker masking were seen in the thalamus, inferior parietal, and anterior cingulate. This study isolated three types of visual processing areas. The first included regions that subserve key stages of vision (including object and motion processing). The second type responded to the presentation of brief ly presented visual stimuli, regardless of masking interval. The third type (selected from the first two) included regions sensitive to the interval between the target and mask. These latter regions (including ventral LO, inferior parietal, anterior cingulate, and thalamus) may form the neural substrate of backward masking.

Decrease and increase in brain activity during visual perceptual priming: An fMRI study on similar but perceptually different complex visual scenes

A robust finding among functional neuroimaging studies on visual priming is decreased neural activity in extrastriate and inferior prefrontal cortices for the second presentation of an object relative to its first presentation. This effect can also be observed for different but perceptually similar objects that are alternative exemplars of the initially presented object (e.g. two different pencils). An unanswered question is whether this decrease in activity can be found for the successive presentation of similar complex visual scenes. We used a test in which landscape pictures were divided vertically into three segments. A first segment was presented and followed several stimuli later by a second related segment. Reaction times were faster for the presentation of the second segment relative to the first one. Although perceptually different from the first segment, the presentation of the second segment was nonetheless associated with reduced activity in late stage visual processing areas including parahippocampal/fusiform gyri bilaterally, left middle occipital and temporal gyri, right inferior temporal and superior occipital gyri, and in left inferior frontal gyrus. The observed decreases in activity in these regions replicate results on priming of different exemplars of single objects while further extending these results to similar complex visual scenes. The presentation of the second segment was also associated with increased activity mainly in frontal and parietal regions, two areas known to be associated with memory retrieval. In sum, priming effects can also occur for complex visual scenes that are intrinsically different from each other although similar in their composition.

Stochastic resonance in the brain

AbstractThis paper investigates the existence of stochastic resonance (SR) in the human brain, based on the noise effect of the α‐wave. In order to show clear evidence of the SR phenomenon in the central nervous system, the measurement was carried out under the following conditions; the periodic and noisy light stimuli are respectively applied to the right and left eye of a subject separately. When the periodic stimulus is applied with a subthreshold condition and the amplitude of noise stimulus of which the frequency bandwidth ranges from 15 to 60 Hz is varied, strong entrainment occurs for a certain range of the noise amplitude. Then the curve for the amplitude of the peak versus the noise amplitude shows a bell‐type shape, that is, the maximum signal amplitude at an optimum noise. Thus, the SR phenomenon occurs not on the retina but on the visual processing area after the optic chiasm—no mixing occurs before primary visual cortex in this manner, because the periodic and random stimuli are separately applied to the right and left eyes, respectively. This result suggests that the human brain may exploit internal and/or external noise for the higher‐order activities such as perception and cognition. © 2004 Wiley Periodicals, Inc. Syst Comp Jpn, 35(11): 39–47, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/scj.10398

Neuroanatomy of adult strabismus: a voxel-based morphometric analysis of magnetic resonance structural scans

Cerebral deficit has been implicated in the genesis of strabismus and in the mechanisms adopted to compensate for the visual disorder. Voxel-based morphometry (VBM) was applied to magnetic resonance images of strabismic adults to detect any abnormal brain anatomy, which could not be easily identified by simple inspection. The gray matter volume in strabismic adults was smaller than that in normal subjects at the areas consistent with the occipital eye field (OEF) and parietal eye field (PEF). However, greater gray matter volume was found in strabismic adults relative to normal controls at the areas consistent with the frontal eye field (FEF), the supplementary eye field (SEF), the prefrontal cortex (PFC), and subcortical regions such as the thalamus and the basal ganglia. These opposite gray matter changes in the visual and the oculomotor processing areas are compatible with a hypothesis of plasticity in the oculomotor regions to compensate for the cortical deficits in the visual processing areas.

Where arousal meets attention: a simultaneous fMRI and EEG recording study

In this fMRI study, we looked for the regions supporting interaction between cortical arousal and attention during three conditions: detection, observation, and rest. Arousal measurements were obtained from the EEG low-frequency (LF) power (5–9.5 Hz) recorded continuously together with fMRI. Whatever the condition, arousal was positively correlated with the fMRI signal of the right dorsal-lateral prefrontal and superior parietal cortices, closely overlapping regions involved in the maintenance of attention. Although the inferior temporal areas also presented a correlation with arousal during detection, path analysis suggests that this influence may be indirect, through the top-down influence of the previously mentioned network. However, those visual-processing areas could account for the correlation between arousal and performances. Lastly, the medial frontal cortex, frontal opercula, and thalamus were inversely correlated with arousal but only during detection and observation so that they could account for the control of arousal.

Neural Correlates of Change Detection and Change Blindness in a Working Memory Task

Detecting changes in an ever-changing environment is highly advantageous, and this ability may be critical for survival. In the present study, we investigated the neural substrates of change detection in the context of a visual working memory task. Subjects maintained a sample visual stimulus in short-term memory for 6 s, and were asked to indicate whether a subsequent, test stimulus matched or did not match the original sample. To study change detection largely uncontaminated by attentional state, we compared correct change and correct no-change trials at test. Our results revealed that correctly detecting a change was associated with activation of a network comprising parietal and frontal brain regions, as well as activation of the pulvinar, cerebellum, and inferior temporal gyrus. Moreover, incorrectly reporting a change when none occurred led to a very similar pattern of activations. Finally, few regions were differentially activated by trials in which a change occurred but subjects failed to detect it (change blindness). Thus, brain activation was correlated with a subject's report of a change, instead of correlated with the physical change per se. We propose that frontal and parietal regions, possibly assisted by the cerebellum and the pulvinar, might be involved in controlling the deployment of attention to the location of a change, thereby allowing further processing of the visual stimulus. Visual processing areas, such as the inferior temporal gyrus, may be the recipients of top-down feedback from fronto-parietal regions that control the reactive deployment of attention, and thus exhibit increased activation when a change is reported (irrespective of whether it occurred or not). Whereas reporting that a change occurred, be it correctly or incorrectly, was associated with strong activation in fronto-parietal sites, change blindness appears to involve very limited territories.

Shared and distinct neurophysiological components of the digits forward and backward tasks as revealed by functional neuroimaging

The digits forward (DF) and backward (DB) tasks are widely used neuropsychological measures believed to tap overlapping systems of phonological processing and working memory. Studies of focal brain lesions have partially elucidated the brain regions essential for these tasks; however relatively little information exists on the underlying functional neuroanatomy in the intact brain. We therefore examined the shared and separate neural systems of these tasks in two positron emission tomography (PET) experiments. In Experiment 1, eight healthy participants performed verbal DF, DB, and a sensorimotor control task during measurement of regional cerebral blood flow (rCBF). DF and DB each activated frontal, parietal, and cerebellar regions as well as prominently activating medial occipital cortex. To eliminate possible visuospatial confounds, Experiment 2 replicated the first experiment in six additional healthy participants who were blindfolded during the study. No differences in activation were found between the two experimental groups. Combined data from both experiments demonstrate that DF and DB rely upon a largely overlapping functional neural system associated with working memory, most notably right dorsolateral prefrontal cortex (DLPFC) and bilateral inferior parietal lobule (IPL) as well as the anterior cingulate, a region associated with attentional effort. The degree of activation increased linearly with increasing task difficulty in DF. DB additionally recruited bilateral DLPFC, left IPL, and Broca’s area. Medial occipital cortex (including higher and lower visual processing areas) was robustly activated in both DF and DB and could not be attributed to visual processing per se, suggesting a possible visual imagery strategy for these aural–verbal tasks.

Cerebral correlates of alerting, orienting and reorienting of visuospatial attention: an event-related fMRI study

The identification of brain systems contributing to different aspects of visuospatial attention is of both clinical and theoretical interest. Cued target detection tasks provide a simple means to dissociate attentional subcomponents, such as alerting, orienting or reorienting of attention. Event-related functional magnetic resonance imaging (fMRI) was used to study neural correlates of these distinct attentional processes. Volunteers were scanned while performing a centrally cued target detection task. Four different types of trials (no cue, neutral cue, valid cue and invalid cue trials) with targets appearing either in the right or left hemifield were randomly intermixed. Behaviourally, the data provided evidence for alerting, spatial orienting and reorienting of attention. Neurally, the alerting effect was seen in bilaterally increased extrastriatal blood oxygenation level-dependent (BOLD) activity in neutral as compared to no cue trials. Neural correlates of spatial orienting were seen in anterior cingulate cortex, which was more active during valid as compared to neutral cue trials. Neural correlates of reorienting of attention, that is, higher BOLD activity to invalid as compared to validly cued trials were evident in several brain regions including left and right intraparietal sulcus, right temporo-parietal junction and middle frontal gyrus bilaterally. The data suggest that frontal and parietal regions are specifically involved in reorienting rather than orienting attention to a spatial position. Alerting effects were seen in extrastriate regions which suggest that increased phasic alertness results in a top–down modulation of neural activity in visual processing areas.

Electrocortical and behavioral effects of chronic immobility on word processing

Neuroelectrical and subjective effects of chronic motor deficits (severe immobility) on word processing were explored. A total of ten artificially ventilated patients with end-stage amyotrophic lateral sclerosis (ALS), seven patients with tetraplegia due to a high spinal cord injury (SCI), and nine matched controls were examined. Both ALS and SCI patients were almost completely paralyzed; eye, head, and face movements were intact in SCI but not in ALS patients. Event-related brain potentials (ERPs) were recorded during presentation of verbs with strong motor-action associations and nouns with strong visual associations. Subjects estimated the subjective strength of motor and visual associations for each word using a scale from 0 to 5. No between-group difference was found for subjectively rated motor associations. All patients reported much stronger visual associations for both nouns and verbs than healthy subjects. ERPs to both word classes revealed a left occipital negativity in SCI patients at a latency of 200–300 ms, and a marked decrease of the slow positive wave in the interval of 300–800 ms in the two patient groups. Both psychophysical and electrophysiological data suggest compensatory activation of visual information processing areas in severely paralyzed patients. The more pronounced effects in the SCI group as compared with the ALS group may be attributed to somatosensory deafferentation in SCI patients, while the sensory inflow in ALS remains relatively intact.

STOCHASTIC RESONANCE IN ALPHA OSCILLATORS IN THE HUMAN BRAIN

We experimentally study stochastic resonance (SR) in the human brain through a noise effect for entrainment dynamics of the alpha (α) wave. The measurement has been carried out under the following conditions in order to obtain clear evidence of the SR phenomenon in the central nervous system. The periodic and noisy stimuli are respectively applied to the right and the left eyes of the subject independently. When only periodic and constant (but weak enough) stimulus is applied to the right eye, it does not induce any global entrainment of α-oscillators to the stimulus frequency. In this situation increasing the amplitude of the noise stimulus (frequency bandwidth from 15 to 60 Hz), harmonic entrainment occurs for a certain range of the noise amplitude and shows a sharp peak in the power spectrum of brain waves. Plotting the amplitude of the peak against the noise amplitude, a bell-type shape is seen, i.e. the maximum signal amplitude at an optimum noise. It clearly indicates the SR phenomenon. Taking account of our experimental conditions and set-up, the present SR phenomenon occurs not on the retina but on the visual processing area in the central nervous systems beyond the optic chiasma.

Unmasking Motion-Processing Activity in Human Brain Area V5/MT+ Mediated by Pathways That Bypass Primary Visual Cortex

Most models of the human visual system argue that higher-order motion-processing cortical regions receive their inputs only via the primary visual cortex (striate cortex), rather than also via direct projections from the thalamus that bypass primary visual cortex. However, recent evidence in non-human primates, along with some evidence in humans with damaged primary visual cortex (e.g., “blindsight” for motion in the blind visual hemifield), have argued for the existence of a direct thalamic-to-extrastriate projection for motion processing. This evidence remains controversial. Here we tested the idea that direct thalamic input to extrastriate motion processing areas exists in humans but might be masked in scalp recordings by activity from early visual areas. To do this, we employed stimuli that induced strong refractory effects in primary visual cortex—thereby creating a brief “reversable lesion” in primary visual cortex—immediately before the presentation of a motion stimulus. Under these conditions, we then assessed whether motion areas of cortex were still able to process the motion stimuli by recording event-related potentials (ERPs) and event-related magnetic fields (ERFs/MEG). We found robust motion-related activity in extrastriate motion processing areas in the ERP and MEG signals even when primary visual cortex was heavily suppressed by our manipulation. This finding provides evidence for a direct thalamic functional pathway to extrastriate visual cortical motion processing areas in the human that bypasses primary visual cortex.

Unmasking Motion-Processing Activity in Human Brain Area V5/MT+ Mediated by Pathways That Bypass Primary Visual Cortex

Most models of the human visual system argue that higher-order motion-processing cortical regions receive their inputs only via the primary visual cortex (striate cortex), rather than also via direct projections from the thalamus that bypass primary visual cortex. However, recent evidence in non-human primates, along with some evidence in humans with damaged primary visual cortex (e.g., “blindsight” for motion in the blind visual hemifield), have argued for the existence of a direct thalamic-to-extrastriate projection for motion processing. This evidence remains controversial. Here we tested the idea that direct thalamic input to extrastriate motion processing areas exists in humans but might be masked in scalp recordings by activity from early visual areas. To do this, we employed stimuli that induced strong refractory effects in primary visual cortex—thereby creating a brief “reversable lesion” in primary visual cortex—immediately before the presentation of a motion stimulus. Under these conditions, we then assessed whether motion areas of cortex were still able to process the motion stimuli by recording event-related potentials (ERPs) and event-related magnetic fields (ERFs/MEG). We found robust motion-related activity in extrastriate motion processing areas in the ERP and MEG signals even when primary visual cortex was heavily suppressed by our manipulation. This finding provides evidence for a direct thalamic functional pathway to extrastriate visual cortical motion processing areas in the human that bypasses primary visual cortex.

The importance of seeing it coming: a functional magnetic resonance imaging study of motion-in-depth towards the human observer

Despite their crucial biological relevance, the neural structures differentially activated by the detection of optic flow towards the observer remain to be elucidated. Here, we deploy functional magnetic resonance imaging with normal volunteers to locate the areas differentially activated when motion towards the observer is detected. Motion towards the observer, compared with motion away, showed significant activations ( P<0.05, corrected for multiple comparisons), as assessed using statistical parametric mapping, in the lateral inferior occipital cortex bilaterally and in right lateral superior occipital cortex. The areas implicated do not extend into area V5 or subdivisions thereof. Our data suggest that the representations of motion towards the observer implicate perceptual and attentional mechanisms acting at early stages of visual processing in extrastriate cortex. From the standpoint of efficient biological engineering, it makes sense that such crucially important functions as object motion towards the observer would be computed in early visual processing areas. Further studies will be required to determine the extent to which the effects we observed in lateral occipital cortex reflect differential attention to different types of motion, as contrasted with the derivation of explicit representations of motion towards the observer.

Noise-induced entrainment and stochastic resonance in human brain waves.

We present the first observation of stochastic resonance (SR) in the human brain's visual processing area. The novel experimental protocol is to stimulate the right eye with a subthreshold periodic optical signal and the left eye with a noisy one. The stimuli bypass sensory organs and are mixed in the visual cortex. With many noise sources present in the brain, higher brain functions, e.g., perception and cognition, may exploit SR.

Neural mechanisms of unconscious visual motion priming

The neural correlates of the motion priming were examined in normal young subjects using event-related brain potentials (ERPs) and functional magnetic resonance imaging (fMRI). Visual motion perception can be unconsciously biased in favor of a particular direction by a preceding motion in that direction. Motion priming first involved an enhancement of ERP amplitude about 100 ms following the onset of motion. The amplitudes of ERP components after 350 ms were also increased. The fMRI results suggest that the early-latency effect reflects modulation of neural responses in extrastriate cortex. Higher-level visual processing areas, including cortical regions MT/MST and the intraparietal cortices were also activated. The findings provide direct evidence that unconscious priming of motion perception is the result of interaction of direction-selective neural responses to motion stimuli. The results cannot be accounted for by refractoriness of neural responses, but instead support a theory of motion priming based on motion opponency, as proposed in computational models.

The Neural Basis of Vertical and Horizontal Line Bisection Judgments: An fMRI Study of Normal Volunteers

Bisection of horizontal lines is used as a clinical test of spatial cognition in patients with left visuospatial neglect after right hemisphere lesions. Bisection of vertical lines has also been employed, albeit less frequently. Interestingly, normal subjects often bisect horizontal lines too far left and vertical lines too high. We used fMRI to investigate whether vertical/horizontal stimulus orientation interacts with the neural mechanisms associated with line bisection judgments (the Landmark task). For control of orientation per se, subjects performed a visual detection task with the same stimuli. Statistical analysis of evoked BOLD responses employed SPM99. The Landmark task increased neural activity (P < 0.05, corrected) in the superior and inferior parietal lobes bilaterally, though predominantly on the right; early visual processing areas bilaterally; and cerebellar vermis, left cerebellar hemisphere, anterior cingulate, and prefrontal cortex bilaterally. Vertical lines (relative to horizontal lines and vice versa) increased neural activity in early visual processing areas, consistent with differential retinotopic stimulation. In addition, vertical lines activated right parietooccipital and superior posterior parietal cortex bilaterally. No significant interactions between the neural mechanisms associated with task and stimuli were observed. Increased neural activation in parietal and parietooccipital cortex associated with vertical lines may reflect increased attentional demands associated with this stimulus orientation. The right hemispheric dominance observed in posterior parietal during the Landmark task irrespective of stimulus orientation is consistent with lesion studies. Our results suggest that the behavioral patterns observed in normal subjects and neurological patients result from different stimulus effects rather than differential task demands.