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ABSTRACT Marmosets are diurnal New World monkeys that show sex-linked cone photopigment polymorphism, whereby all males and some females are dichromats ("red-green colorblind"), but most females show trichromatic color vision. Here we asked whether trichromats express chromatic-specific circuitry in the lateral geniculate nucleus (LGN). The volume of parvocellular (P), magnocellular (M), and koniocellular (K) layers was calculated in Nissl-stained sections from the LGN of adult marmosets ( Callithrix jacchus; 10 trichromatic females; 2 dichromatic females; and 13 dichromatic males). Retinal ganglion cell axon terminals within the P and K layers were reconstructed and measured following anterograde tracer (dextran) injections. We show that there is little difference in LGN layer volume with respect to age, weight, or sex of the animals, or between dichromatic and trichromatic phenotypes. The morphology of retinal ganglion cell terminals was largely indistinguishable on comparing dichromats and trichromats, and likewise on comparing terminals representing peripheral or foveal retina. We conclude that the LGN circuits we studied are largely independent of red-green color vision phenotype and visual field location. J. Comp. Neurol. 523:1948-1966, 2015 © 2015 Wiley Periodicals, Inc. [ABSTRACT FROM AUTHOR]

Visual perception changes as a function of hand proximity. While various theoretical accounts have been offered for this alteration (attentional prioritisation, bimodal cell involvement, detailed evaluation, and magnocellular neuron input enhancement), the current literature lacks consensus on these mechanisms. The purpose of this review, therefore, is to critically review the existing body of literature in light of these distinct theoretical accounts. We find that a growing number of results support the magnocellular (M-cell) enhancement account, and are difficult to reconcile with general attention-based explanations. Despite this key theoretical development in the field, there has been some ambiguity with interpretations offered in recent papers, for example, equating the existing attentional and M-cell based explanations, when in fact they make contrasting predictions. We therefore highlight the differential predictions arising from the distinct theoretical accounts. Importantly, however, we also offer novel perspectives that synthesises the role of attention and neurophysiological mechanisms in understanding altered visual perception near the hands. We envisage that this theoretical development will ensure that the field can progress from documenting behavioural differences, to a consensus on the underlying visual and neurophysiological mechanisms. [ABSTRACT FROM AUTHOR]

Paying attention to visual stimuli is typically accompanied by event-related desynchronizations (ERD) of ongoing alpha (7-14 Hz) activity in visual cortex. The present study used time-frequency based analyses to investigate the role of impaired alpha ERD in visual processing deficits in schizophrenia (Sz). Subjects viewed sinusoidal gratings of high (HSF) and low (LSF) spatial frequency (SF) designed to test functioning of the parvo- vs. magnocellular pathways, respectively. Patients with Sz and healthy controls paid attention selectively to either the LSF or HSF gratings which were presented in random order. Event-related brain potentials (ERPs) were recorded to all stimuli. As in our previous study, it was found that Sz patients were selectively impaired at detecting LSF target stimuli and that ERP amplitudes to LSF stimuli were diminished, both for the early sensory-evoked components and for the attend minus unattend difference component (the Selection Negativity), which is generally regarded as a specific index of feature-selective attention. In the time-frequency domain, the differential ERP deficits to LSF stimuli were echoed in a virtually absent theta-band phase locked response to both unattended and attended LSF stimuli (along with relatively intact theta-band activity for HSF stimuli). In contrast to the theta-band evoked responses which were tightly stimulus locked, stimulus-induced desynchronizations of ongoing alpha activity were not tightly stimulus locked and were apparent only in induced power analyses. Sz patients were significantly impaired in the attention-related modulation of ongoing alpha activity for both HSF and LSF stimuli. These deficits correlated with patients' behavioral deficits in visual information processing as well as with visually based neurocognitive deficits. These findings suggest an additional, pathway-independent, mechanism by which deficits in early visual processing contribute to overall cognitive impairment in Sz. [ABSTRACT FROM AUTHOR]

Dyslexia is a specific impairment in reading that affects 1 in 10 people. Previous studies have failed to isolate a single cause of the disorder, but several candidate genes have been reported. We measured motion perception in two groups of dyslexics, with and without a deletion within the DCDC2 gene, a risk gene for dyslexia. We found impairment for motion particularly strong at high spatial frequencies in the population carrying the deletion. The data suggest that deficits in motion processing occur in a specific genotype, rather than the entire dyslexia population, contributing to the large variability in impairment of motion thresholds in dyslexia reported in the literature. [ABSTRACT FROM AUTHOR]

A number of authors have postulated a “magnocellular-dorsal stream” deficit in dyslexia. Combining the magnocellular system and the dorsal stream into a single entity in this context faces the problem that contrast sensitivity data do not point to a magnocellular deficiency linked to dyslexia, while, on the other hand, motion perception data are largely consistent with a dorsal stream dysfunction. Thus, there are data both for and against a “magnocellular-dorsal stream” deficit in connection with dyslexia. It is here pointed out that this inconsistency is abolished once it is recognized that the magnocellular system and the dorsal stream are separate entities. [ABSTRACT FROM AUTHOR]

Superior local at the expense of global perception characterises vision in autism spectrum disorders (ASD). However, progress towards discovering a neural mechanism has been slow. Here we used known differences in magnocellular and parvocellular receptive field properties to assess the temporal encoding of information, via flicker fusion paradigms, in those high and low in self-reported autistic tendency (Autism Spectrum Quotient – AQ). A Low AQ group (AQ≤13, n =22), and a High AQ group (AQ≥18, n =17) undertook a 4AFC luminance flicker fusion (FF) with 5 temporal contrasts from 5% to 100%, and a 2AFC isoluminant red–green colour fusion task. Both groups showed an increase in fusion thresholds with temporal achromatic contrast. The High AQ group displayed diminished flicker fusion thresholds compared to the Low AQ at the lowest contrasts. For the red–green colour fusion task, the High AQ group displayed mean fusion frequency slightly greater than the Low AQ group. A significant interaction between 5% luminance contrast and the red–green fusion frequencies demonstrated that the differences in thresholds were not simply due to variations in overall attentional capacity between groups. These differences in flicker fusion thresholds are in accordance with reported differences in cortical visual evoked potential nonlinearities, particularly relating to the neural efficiency of the magnocellular pathway. [ABSTRACT FROM AUTHOR]

Background: Individuals with schizophrenia spectrum diagnoses have deficient visual information processing as assessed by a variety of paradigms including visual backward masking, motion perception and visual contrast sensitivity (VCS). In the present study, the VCS paradigm was used to investigate potential differences in magnocellular (M) versus parvocellular (P) channel function that might account for the observed information processing deficits of schizophrenia spectrum patients. Specifically, VCS for near threshold luminance (black/white) stimuli is known to be governed primarily by the M channel, while VCS for near threshold chromatic (red/green) stimuli is governed by the P channel. Methods: VCS for luminance and chromatic stimuli (counterphase-reversing sinusoidal gratings, 1.22 c/deg, 8.3 Hz) was assessed in 53 patients with schizophrenia (including 5 off antipsychotic medication), 22 individuals diagnosed with schizotypal personality disorder and 53 healthy comparison subjects. Results: Schizophrenia spectrum groups demonstrated reduced VCS in both conditions relative to normals, and there was no significant group by condition interaction effect. Post-hoc analyses suggest that it was the patients with schizophrenia on antipsychotic medication as well as SPD participants who accounted for the deficits in the luminance condition. Conclusions: These results demonstrate visual information processing deficits in schizophrenia spectrum populations but do not support the notion of selective abnormalities in the function of subcortical channels as suggested by previous studies. Further work is needed in a longitudinal design to further assess VCS as a vulnerability marker for psychosis as well as the effect of antipsychotic agents on performance in schizophrenia spectrum populations.

Studies have shown that patients with schizophrenia exhibit visual processing impairments, particularly regarding the processing of spatial frequencies. In a previous work, we found that, compared to healthy volunteers, patients were biased towards low spatial frequencies (LSF) to identify facial expression at a glance. Given the ubiquity of faces in visual perception, it remains an open question whether the LSF bias is face specific or also occurs with other visual objects. Here, fifteen patients with schizophrenia and eleven healthy control adults performed a categorization task with hybrid stimuli. These stimuli were single images consisting of two different objects, a fruit and an animal, each in a specific spatial frequency range, either low (LSF) or high (HSF). Observers were asked to report if they saw an animal or a fruit. The reported category demonstrated which spatial scale was preferentially perceived in each trial. In a control experiment, participants performed the same task but with images of only a single object, either a LSF or HSF filtered animal or fruit, to verify that participants could perceive both HSF or LSF when presented in isolation. The results on the categorization task showed that patients chose more frequently LSF with hybrid stimuli compared to healthy controls. However, both populations performed equally well with HSF and LSF filtered pictures in the control experiment, demonstrating that the LSF preference found with hybrid stimuli in patients was not due to an inability to perceive HSF.The LSF preference found in schizophrenia confirms our previous study conducted with faces, and shows that this LSF bias generalizes to other categories of objects. When a broad range of spatial frequencies are present in the image, as in normal conditions of viewing, patients preferentially rely on coarse visual information contained in LSF. This result may be interpreted as a dysfunction of the guidance of HSF processing by LSF processing.

When two sufficiently different stimuli are presented to each eye, perception alternates between them. This binocular rivalry is conceived as a competition for representation in the single stream of visual consciousness. The magnocellular (M) and parvocellular (P) pathways, originating in the retina, encode disparate information, but their potentially different contributions to binocular rivalry have not been determined. Here, we used functional magnetic resonance imaging to measure the human lateral geniculate nucleus (LGN), where the M and P neurons are segregated into layers receiving input from a single eye. We had three participants (one male, two females) and used achromatic stimuli to avoid contributions from color opponent neurons that may have confounded previous studies. We observed activity in the eye-specific regions of LGN correlated with perception, with similar magnitudes during rivalry or physical stimuli alternations, also similar in the M and P regions. These results suggest that LGN activity reflects our perceptions during binocular rivalry and is not simply an artifact of color opponency. Further, perception appears to be a global phenomenon in the LGN, not just limited to a single information channel., Competing Interests: The authors declare no competing financial interests., (Copyright © 2023 Yildirim and Schneider.)

A growing body of evidence indicates that the perception of visual stimuli is altered when they occur near the observer's hands, relative to other locations in space (see Brockmole, Davoli, Abrams, & Witt, , for a review). Several accounts have been offered to explain the pattern of performance across different tasks. These have typically focused on attentional explanations (attentional prioritization and detailed attentional evaluation of stimuli in near-hand space), but more recently, it has been suggested that near-hand space enjoys enhanced magnocellular (M) input. Here we differentiate between the attentional and M-cell accounts, via a task that probes the roles of position consistency and color consistency in determining dynamic object correspondence through occlusion. We found that placing the hands near the visual display made observers use only position consistency, and not color, in determining object correspondence through occlusion, which is consistent with the fact that M cells are relatively insensitive to color. In contrast, placing observers' hands far from the stimuli allowed both color and position contribute. This provides evidence in favor of the M-cell enhancement account of altered vision near the hands. [ABSTRACT FROM AUTHOR]

It is well-known the advantages of measuring chromatic and achromatic contrast sensitivity for detecting pathologies. But these measurements are rarely used in clinical practice, due the complexity of the measurements and the examinator specialization. In fact, there is not a complete characterization of the response of the visual pathways to achromatic and chromatic spatio-temporal frequency stimuli. We have designed a new experimental device that facilitates these measurements and allow us to characterize the visual response in healthy patients. In this paper, we evaluated the responses of the visual pathways in healthy patients. [ABSTRACT FROM AUTHOR]

The magnocellular (M) and parvocellular (P) subdivisions of primate LGN are known to process complementary types of visual stimulus information, but a method for noninvasively defining these subdivisions in humans has proven elusive. As a result, the functional roles of these subdivisions in humans have not been investigated physiologically. To functionally map the M and P subdivisions of human LGN, we used high-resolution fMRI at high field (7 T and 3 T) together with a combination of spatial, temporal, luminance, and chromatic stimulus manipulations. We found that stimulus factors that differentially drive magnocellular and parvocellular neurons in primate LGN also elicit differential BOLD fMRI responses in human LGN and that these responses exhibit a spatial organization consistent with the known anatomical organization of the M and P subdivisions. In test–retest studies, the relative responses of individual voxels to M-type and P-type stimuli were reliable across scanning sessions on separate days and across sessions at different field strengths. The ability to functionally identify magnocellular and parvocellular regions of human LGN with fMRI opens possibilities for investigating the functions of these subdivisions in human visual perception, in patient populations with suspected abnormalities in one of these subdivisions, and in visual cortical processing streams arising from parallel thalamocortical pathways. [ABSTRACT FROM AUTHOR]

Glutamate is used as an excitatory neurotransmitter by the koniocellular (K), magnocellular (M), and parvocellular (P) pathways to transfer signals from the primate lateral geniculate nucleus (LGN) to primary visual cortex (V1). Glutamate acts through both fast ionotropic receptors, which appear to carry the main sensory message, and slower, modulatory metabotropic receptors (mGluRs). In this study, we asked whether mGluR5 relates in distinct ways to the K, M, and P LGN axons in V1. To answer this question, we used light microscopic immunocytochemistry and preembedding electron microscopic immunogold labeling to determine the localization of mGluR5 within the layers of V1 in relation to the K, M, and P pathways in macaque and squirrel monkeys. These pathways were labeled separately via wheat germ agglutinin–horseradish peroxidase (WGA–HRP) injections targeting the LGN layers. mGluR5 is of interest because it: 1) has been shown to be expressed in the thalamic input layers; 2) appears to be responsible for some types of oscillatory firing, which could be important in the binding of visual features; and 3) has been associated with a number of sensory-motor gating-related pathologies, including schizophrenia and autism. Our results demonstrated the presence of mGluR5 in the neuropil of all V1 layers. This protein was lowest in IVCα (M input) and the infragranular layers. In layer IVC, mGluR5 also was found postsynaptic to about 30% of labeled axons, but the distribution was uneven, such that postsynaptic mGluR5 label tended to occur opposite smaller (presumed P), and not larger (presumed M) axon terminals. Only in the K pathway in layer IIIB, however, was mGluR5 always found in the axon terminals themselves. The presence of mGluR5 in K axons and not in M and P axons, and the presence of mGluR5 postsynaptic mainly to smaller P and not larger M axons suggest that the response to the release of glutamate is modulated in distinct ways within and between the parallel visual pathways of primates. [ABSTRACT FROM AUTHOR]

Crossmodal interaction conferring enhancement in sensory processing is nowadays widely accepted. Such benefit is often exemplified by neural response amplification reported in physiological studies conducted with animals, which parallel behavioural demonstrations of sound-driven improvement in visual tasks in humans. Yet, a good deal of controversy still surrounds the nature and interpretation of these human psychophysical studies. Here, we consider the interpretation of crossmodal enhancement findings under the light of the functional as well as anatomical specialization of magno- and parvocellular visual pathways, whose paramount relevance has been well established in visual research but often overlooked in crossmodal research. We contend that a more explicit consideration of this important visual division may resolve some current controversies and help optimize the design of future crossmodal research. [ABSTRACT FROM AUTHOR]

The human visual system is continuously confronted with dynamic visual input. One challenge that the visual system must solve, therefore, is recognizing when two distinct objects have appeared at a given location despite their brief presentation and rapid succession, that is, temporal object segmentation. Here we examined the role of magnocellular neurons in this process. We measured temporal object segmentation via object substitution masking (OSM), which reflects the failure to distinguish the target and mask as distinct objects through time. We isolated the selective role of magnocellular neurons by comparing performance under conditions of pulsed luminance pedestals, which are designed to saturate the magnocellular response, with that in a steady-pedestal condition that leaves both magnocellular and parvocellular channels available to process the target. Across two experiments, we found that OSM magnitude was enhanced under pulsed-pedestal conditions, in which the magnocellular response was impaired. This indicates that magnocellular neurons contribute to temporal object segmentation. Given that temporal object segmentation has consequences for which stimuli are consciously perceived, this demonstrates a functional mechanism via which magnocellular neurons contribute to determining the contents conscious perception. Implications for models of specialization of dorsal and ventral cortical streams are discussed. [ABSTRACT FROM AUTHOR]

Objectives While cognitive deficits have been well documented in patients with bipolar disorder, visual perception has been less well characterized. Such deficits appear in schizophrenia, which shares genetic risk factors with bipolar disorder, and may contribute to disturbances in visual cognition and learning. Methods The present study investigated visual perception in bipolar disorder using psychophysical tests of contrast sensitivity, dot motion discrimination, and form discrimination. The relationship of these measures to mood state, medication status, and cognitive function was investigated. Sixty-one patients with type I bipolar disorder and 67 comparison subjects were tested. Results Results indicated a deficit in dot motion trajectory discrimination in both euthymic and ill individuals with bipolar disorder, as well as a global deficit in moving grating contrast sensitivity. Ill individuals with bipolar disorder were impaired in psychomotor processing, but this finding was not related to visual processing performance. Conclusions These findings could be due to disturbances in specific visual pathways involved in the processing of motion properties, or to a more general deficit which impairs processing of temporally modulated stimuli. [ABSTRACT FROM AUTHOR]

Abstract: It has been proposed that magno- and parvocellular contributions to Visually Evoked Potentials (VEPs) can be isolated, or differentiated, by noting the contrast–response relationships of the responses. This suggestion is examined quantitatively by determining the similarity between various sets of VEP data that have been attributed to the magno- and parvocellular systems and previously reported contrast–response functions for different kinds of neurons (magno- and parvocellular neurons and V1, V4, and MT cells) and combinations of the contrast–response functions for these neurons. It is found that other neurons, or combinations of other neurons, typically give better fits to the data than do magno- and parvocellular cells. Thus, to attribute VEP responses to the magno- or parvocellular systems based on contrast–responses properties faces difficulties. [Copyright &y& Elsevier]

Phonological and visual dysfunctions may result in reading deficits like those encountered in developmental dyslexia. Here, we use a novel approach to induce similar reading difficulties in normal readers in an event-related fMRI study, thus systematically investigating which brain regions relate to different pathways relating to orthographic-phonological (e.g. grapheme-to-phoneme conversion, GPC) vs. visual processing. Based upon a previous behavioural study (Tholen et al. ), the retrieval of phonemes from graphemes was manipulated by lowering the identifiability of letters in familiar vs. unfamiliar shapes. Visual word and letter processing was impeded by presenting the letters of a word in a moving, non-stationary manner. FMRI revealed that the visual condition activated cytoarchitectonically defined area hOC5 in the magnocellular pathway and area 7A in the right mesial parietal cortex. In contrast, the grapheme manipulation revealed different effects localised predominantly in bilateral inferior frontal gyrus (left cytoarchitectonic area 44; right area 45) and inferior parietal lobule (including areas PF/PFm), regions that have been demonstrated to show abnormal activation in dyslexic as compared to normal readers. This pattern of activation bears close resemblance to recent findings in dyslexic samples both behaviourally and with respect to the neurofunctional activation patterns. The novel paradigm may thus prove useful in future studies to understand reading problems related to distinct pathways, potentially providing a link also to the understanding of real reading impairments in dyslexia. [ABSTRACT FROM AUTHOR]

Both theoretical and experimental evidence suggests that duration perception is mediated preferentially by the colour-blind but high temporally sensitive luminance pathway. In this experiment we tested whether colour modulated stimuli and high spatial frequency luminance modulated stimuli, which are known to be relayed mostly by the slow parvocellular system, are able to elicit reliable sense of duration. We show that ramped colour modulated stimuli seem to last less than luminance modulated stimuli matched for visibility. The effect is large, about 200 ms and is constant at all durations tested (range 500 - 1100 ms). However high spatial frequency luminance stimuli obtain duration matches similar to those of low spatial frequency luminance modulated stimuli. The results at various levels of contrast and temporal smoothing indicate that equiluminant stimuli have higher contrast thresholds to activate the mechanisms which time visual stimuli. Overall the results imply that both the magnocellular and the parvocellular systems access reliably the timing mechanisms with a difference only in the way these are engaged.

An influential theory in the field of visual object recognition proposes that it is the fast magnocellular (M) system that facilitates neural processing of spatially more fine-grained information rather the slower parvocellular (P) system. While written words can be considered as a special type of visual objects, it is unknown whether magnocellular facilitation also plays a role in reading. We used a masked priming paradigm that has been shown to result in neural facilitation in visual word processing and tested whether these facilitating effects are mediated by the magnocellular system. In two experiments, we manipulated the influence of magnocellular and parvocellular systems on visual processing of a contextually predictable target character by contrasting high versus low spatial frequency and luminance versus color contrast, respectively. In addition, unchanged (normal) primes were included in both experiments as a manipulation check. As expected, unchanged primes elicited typical repetition effects in the N1, N250 and P3 components of the ERP in both experiments. In the experiment manipulating spatial contrast, we obtained repetition effects only for the N1 component for both M- and P-biased primes. In the luminance versus color contrast experiment, repetition effects were found in N1 and N250 for both M- and P- biased primes. Furthermore, no interactions were found between M-vs. P-biased prime types and repetition. Together these results indicate that M- and P- information contributes jointly to early neural processes underlying visual word recognition. • Masked repetition priming is indicated by N1/P3 increase and N250 decrease. • Magnocellular M and parvocellular P primes were tested under expectation inducement. • M- and P-primes based on spatial frequency show N1 repetition effects. • M- and P-primes based on luminance/color show N1 and N250 repetition effects. • Similar masked priming effects for M- and P-primes despite expectation inducement. [ABSTRACT FROM AUTHOR]

Highlights: [•] Patients with schizophrenia demonstrated impaired frequency doubling illusion compared to normal controls. [•] Impaired frequency doubling illusion in patients with schizophrenia might be attributed to a magnocellular pathway deficit. [•] A magnocellular pathway deficit can explain some cognitive dysfunctions in patients with schizophrenia. [Copyright &y& Elsevier]

A key feature of early visual cortical regions is that they contain discretely organized retinotopic maps. Titration of these maps must occur through experience, and the fidelity of their spatial tuning will depend on the consistency and accuracy of the eye movement system. Anomalies in fixation patterns and the ballistics of eye movements are well documented in autism spectrum disorder ( ASD), with off-center fixations a hallmark of the phenotype. We hypothesized that these atypicalities might affect the development of visuo-spatial maps and specifically that peripheral inputs might receive altered processing in ASD. Using high-density recordings of visual evoked potentials ( VEPs) and a novel system-identification approach known as VESPA (visual evoked spread spectrum analysis), we assessed sensory responses to centrally and peripherally presented stimuli. Additionally, input luminance was varied to bias responsiveness to the magnocellular system, given previous suggestions of magnocellular-specific deficits in ASD. Participants were 22 ASD children (7-17 years of age) and 31 age- and performance- IQ-matched neurotypical controls. Both VEP and VESPA responses to central presentations were indistinguishable between groups. In contrast, peripheral presentations resulted in significantly greater early VEP and VESPA amplitudes in the ASD cohort. We found no evidence that anomalous enhancement was restricted to magnocellular-biased responses. The extent of peripheral response enhancement was related to the severity of stereotyped behaviors and restricted interests, cardinal symptoms of ASD. The current results point to differential visuo-spatial cortical mapping in ASD, shedding light on the consequences of peculiarities in gaze and stereotyped visual behaviors often reported by clinicians working with this population. [ABSTRACT FROM AUTHOR]

Metacontrast is a form of visual masking in which the target and mask are non-overlapping. In metacontrast, the masking effect is typically largest when the mask is presented some time after the target. This is known as Type-B masking. The present report examines to what extent Type-B metacontrast masking can be explained based on the stimuli involved. The assumption is made that the visibility of the target is, at least in part, determined by the correlation between the amplitude spectrum of the target-and-mask combination and that of the target alone. It is found that the correlation is higher when the stimuli are presented at the same time relative to when they are presented at different times. This relationship follows from the stimuli alone. Thus, one would expect the masking to be weakest when the two stimuli are simultaneous. Type-B correlation functions, in which the largest reductions occur only when the mask is presented after the target, can be obtained by further assuming a temporal integration window with a rapid onset and a shallow decline. In agreement with psychophysical masking studies; the analyses yield functions that are most similar to Type-B masking for moderate mask intensities and become less Type-B like at higher mask intensities. The effects of dark adaptation and spatial separation of target and mask are also modeled. [ABSTRACT FROM AUTHOR]

Abstract: In order to investigate the effects of visual experience on early visual development, the current study compared contrast sensitivity across infants born with different degrees of moderate-to-late prematurity. Here the logic is that at any given postterm age, the most premature infants will have the oldest postnatal age. Given that postnatal age is a proxy for visual experience, the visual experience hypothesis predicts that infants who are more premature, yet healthy, should have higher sensitivity. Luminance (light/dark) and chromatic (red/green) contrast sensitivities (CS) were measured in 236 healthy infants (born −10 to +2weeks relative to due date) between 5 and 32weeks postterm age from due date and 8–38weeks postnatal from birth date. For chromatic CS, we found clear evidence that infants who were most premature within our sample had the highest sensitivity. Specifically, 4–10 additional weeks of visual experience, by virtue of being born early, enhanced chromatic CS. For luminance CS, similar but weaker results were seen. Here, only infants with an additional 6–10weeks of visual experience, and only at later age points in development, showed enhanced sensitivity. However, CS in preterm infants was still below that of fullterm infants with equivalent postnatal age. In sum, these results suggest that chromatic CS is influenced more by prematurity (and possibly visual experience) than luminance CS, which has implications for differential development of parvocellular and magnocellular pathways. [Copyright &y& Elsevier]

Abstract: Atypical high-level vision in autism is sometimes attributed to a core deficit in the function of lateral geniculate nucleus magnocells or their retinal drives. While some physiological measures provide indirect, suggestive evidence for such a deficit, support from behavioural measures is lacking and contradictory. We assessed luminance contrast increment thresholds on pulsed- and steady- pedestals in 17 children with autism spectrum conditions (ASC) compared to 17 typically developing children; these two conditions correspond to widely-used indices of magnocellular and parvocellular function. As a group, children with ASC had strikingly elevated thresholds on the steady pedestal-paradigm, yet performed similarly to controls on the pulsed pedestal paradigm, a finding that would typically be interpreted to reflect impaired magnocellular function. The effect size of the impairment was large and a substantial minority (41.2%) of the ASC group showed significantly impaired performance on an individual basis. This finding is consistent with a selective magnocellular deficit. It directly contradicts previous claims that such deficits are confined to ‘complex’ visual stimuli and likely does not reflect atypical attention, adaptation or high-level vision. The pattern of results is not clearly predicted by notions of imbalance of excitation versus inhibition, atypical lateral connectivity or enhanced perceptual function that account for a range of other findings associated with perception in autism. It may be amenable to explanation in terms of decreased endogenous neural noise, a novel alternative we outline here. [Copyright &y& Elsevier]

Abstract: Perception has been identified by the NIMH-sponsored Cognitive Neuroscience Treatment Research to Improve Cognition in Schizophrenia (CNTRICS) group as a useful domain for assessing cognitive deficits in patients with schizophrenia. Specific measures of contrast gain derived from recordings of steady-state visual evoked potentials (ssVEP) have demonstrated neural deficits within the visual pathways of patients with schizophrenia. Psychophysical measures of contrast sensitivity have also shown functional loss in these patients. In the current study, functional magnetic resonance imaging (fMRI) was used in conjunction with ssVEP and contrast sensitivity testing to elucidate the neural underpinnings of these deficits. During fMRI scanning, participants viewed 1) the same low and higher spatial frequency stimuli used in the psychophysical contrast sensitivity task, at both individual detection threshold contrast and at a high contrast; and 2) the same stimuli used in the ssVEP paradigm, which were designed to be biased toward either the magnocellular or parvocellular visual pathway. Patients showed significant impairment in contrast sensitivity at both spatial frequencies in the psychophysical task, but showed reduced occipital activation volume for low, but not higher, spatial frequency at the low and high contrasts tested in the magnet. As expected, patients exhibited selective deficits under the magnocellular-biased ssVEP condition. However, occipital lobe fMRI responses demonstrated the same general pattern for magnocellular- and parvocellular-biased stimuli across groups. These results indicate dissociation between the fMRI measures and the psychophysical/ssVEP measures. These latter measures appear to have greater value for the functional assessment of the contrast deficits explored here. [Copyright &y& Elsevier]

Foveated stimuli receive visual processing that is quantitatively and qualitatively different from nonfoveated stimuli. At normal interpersonal distances, people move their eyes around another’s face so that certain features receive foveal processing; on any given fixation, other features therefore project extrafoveally. Yet little is known about the processing of extrafoveally presented facial features, how informative those extrafoveally presented features are for face perception (e.g., for assessing another’s emotion), or what processes extract task-relevant (e.g., emotion-related) cues from facial features that first appear outside the fovea, and how these processes are implemented in the brain. [ABSTRACT FROM PUBLISHER]

Abstract: The pulsed-pedestal paradigm consists of the simultaneous brief presentation of a test stimulus and luminance pedestals. Processing with this paradigm is thought to be mediated by the parvocellular pathway. The steady-pedestal paradigm consists of the brief presentation of a test stimulus against a continuously presented luminance pedestals. Processing with this paradigm is thought to be mediated by the magnocellular pathway. To test the prediction that transient attention should have a differential effect on performance with these two paradigms, we added to their typical procedures peripheral precues that trigger transient attention. As expected, we have found that the attraction of transient attention to the target location improved performance with the pulsed-pedestal paradigm, but had no reliable effect on performance with the steady-pedestal paradigm. These findings support the hypothesis that transient attention favors parvocellular over magnocellular processing. [Copyright &y& Elsevier]

The aim was to investigate the temporal response properties of magnocellular, parvocellular, and koniocellular visual pathways using increment/decrement changes in contrast to elicit visual evoked potentials (VEPs). Static achromatic and isoluminant chromatic gratings were generated on a monitor. Chromatic gratings were modulated along red/green (R/G) or subject-specific tritanopic confusion axes, established using a minimum distinct border criterion. Isoluminance was determined using minimum flicker photometry. Achromatic and chromatic VEPs were recorded to contrast increments and decrements of 0.1 or 0.2 superimposed on the static gratings (masking contrast 0–0.6). Achromatic increment/decrement changes in contrast evoked a percept of apparent motion when the spatial frequency was low; VEPs to such stimuli were positive in polarity and largely unaffected by high levels of static contrast, consistent with transient response mechanisms. VEPs to finer achromatic gratings showed marked attenuation as static contrast was increased. Chromatic VEPs to R/G or tritan chromatic contrast increments were of negative polarity and showed progressive attenuation as static contrast was increased, in keeping with increasing desensitization of the sustained responses of the color-opponent visual pathways. Chromatic contrast decrement VEPs were of positive polarity and less sensitive to pattern adaptation. The relative contribution of sustained/transient mechanisms to achromatic processing is spatial frequency dependent. Chromatic contrast increment VEPs reflect the sustained temporal response properties of parvocellular and koniocellular pathways. Cortical VEPs can provide an objective measure of pattern adaptation and can be used to probe the temporal response characteristics of different visual pathways. [ABSTRACT FROM AUTHOR]

The sensory abnormalities associated with disorders such as dyslexia, autism and schizophrenia have often been attributed to a generalized deficit in the visual magnocellular–dorsal stream and its auditory homologue. To probe magnocellular function, various psychophysical tasks are often employed that require the processing of rapidly changing stimuli. But is performance on these several tasks supported by a common substrate? To answer this question, we tested a cohort of 1060 individuals on four ‘magnocellular tasks’: detection of low-spatial-frequency gratings reversing in contrast at a high temporal frequency (so-called frequency-doubled gratings); detection of pulsed low-spatial-frequency gratings on a steady luminance pedestal; detection of coherent motion; and auditory discrimination of temporal order. Although all tasks showed test–retest reliability, only one pair shared more than 4 per cent of variance. Correlations within the set of ‘magnocellular tasks’ were similar to the correlations between those tasks and a ‘non-magnocellular task’, and there was little consistency between ‘magnocellular deficit’ groups comprising individuals with the lowest sensitivity for each task. Our results suggest that different ‘magnocellular tasks’ reflect different sources of variance, and thus are not general measures of ‘magnocellular function’. [ABSTRACT FROM AUTHOR]

Developmental dyslexia, a severe and persistent reading and spelling impairment. Is characterized by difficulties in processing speech sounds (i.e., phonemes). Here, we test the hypothesis that these phonological difficulties are associated with a dysfunction of the auditory sensory thalamus, the medial geniculate body (MGB). By using functional MRI, we found that, in dyslexic adults, the MGB responded abnormally when the task required attending to phonemes compared with other speech features. No other structure in the auditory pathway showed distinct functional neural patterns between the two tasks for dyslexic and control participants. Furthermore, MGB activity correlated with dyslexia diagnostic scores, indicating that the task modulation of the MGB is critical for performance in dyslexies. These results suggest that deficits in dyslexia are associated with a failure of the neural mechanism that dynamically tunes MGB according to predictions from cortical areas to optimize speech processing. This view on task-related MGB dysfunction in dyslexies has the potential to reconcile influential theories of dyslexia within a predictive coding framework of brain function. [ABSTRACT FROM AUTHOR]

Abstract: The present study investigated the mechanisms responsible for the difference between visual processing of stimuli near and far from the observer’s hands. The idea that objects near the hands are immediate candidates for action led us to hypothesize that vision near the hands would be biased toward the action-oriented magnocellular visual pathway that supports processing with high temporal resolution but low spatial resolution. Conversely, objects away from the hands are not immediate candidates for action and, therefore, would benefit from a bias toward the perception-oriented parvocellular visual pathway that supports processing with high spatial resolution but low temporal resolution. We tested this hypothesis based on the psychophysical characteristics of the two pathways. Namely, we presented subjects with two tasks: a temporal-gap detection task which required the high temporal acuity of the magnocellular pathway and a spatial-gap detection task that required the spatial acuity of the parvocellular pathway. Consistent with our prediction, we found better performance on the temporal-gap detection task and worse performance on the spatial-gap detection task when stimuli were presented near the hands compared to when they were far from the hands. These findings suggest that altered visual processing near the hands may be due to changes in the contribution of the two visual pathways. [Copyright &y& Elsevier]

Abstract: Controversy still exists over whether there is a magnocellular deficit associated with developmental dyslexia. Here we utilised a magnocellular system-biased phantom contour form discrimination task defined by high temporal frequency contrast reversals to compare contrast sensitivity in a group of children with dyslexia and an age- and nonverbal intelligence-matched control group (9–14 years). Stimuli were either abruptly presented for 4 refresh frames (34ms), or in two reduced transience conditions had contrast progressively ramped on and off over either 4 frames or 10 frames (86ms). Children in the dyslexia group showed increased contrast thresholds compared with the control group in all three conditions, and thus strong evidence for a magnocellular deficit. Although the absolute size of the differences in threshold scores between control and dyslexic groups increased dramatically between the abrupt and the 4 and 10 frame ramped onset stimuli, the similar effect size across all tasks, and also the similar range of contrast change at the first frame of stimulus presentation across all tasks between groups suggests that a similar neural mechanism could provide the locus of the apparent magnocellular deficit in children with dyslexia for all tasks tested. These results suggest that threshold discrimination of stimuli with low contrast and high temporal frequencies designed to target the magnocellular system, and has great potential for early screening for children at risk of visually derived reading difficulties. [Copyright &y& Elsevier]

Abstract: In an experimental paradigm adapted from , forty observers listened via headphones to 8 binaural clicks: 4 left-ear leading followed by 4 right-ear leading with either 38 or 140ms interstimulus intervals (ISIs). Concurrently, they viewed either foveal or peripheral visual stimuli designed to activate either the parvocellular or magnocellular pathway. They then reported the perceived location of each click-pair. Our results replicated Hari’s finding that observers mistake the perceived location of short ISI click-pairs more often than long. That is, when ISIs were short, the sounds seemed to play across the inside of the head in a phenomenon called illusory directional hearing. However, when click-pairs were accompanied by peripheral visual stimuli that activated the magnocellular pathway, observers were more accurate than when there were no visual stimuli. Conversely, parvocellular-activating foveal visual stimuli produced more illusory hearing than when there were no visual stimuli. These findings suggest that activating the slow sustained parvocellular system may result in a longer processing window. Thirty dyslexic observers who repeated the experimental paradigm had an even longer processing window than control observers indicating that dyslexics may have a magnocellular system deficit. [Copyright &y& Elsevier]

Abstract: Vernier thresholds are known to be elevated when a target pair has opposite contrast polarity. Polarity reversal is used to assess the role of luminance and chromatic pathways in hyperacuity performance. Psychophysical hyperacuity thresholds were measured for pairs of gratings of various combinations of luminance (Lum) and chromatic (Chr) contrast polarities, at different ratios of luminance to chromatic contrast. With two red–green gratings of matched luminance and chromatic polarity (+Lum+Chr), there was an elevation of threshold at isoluminance. When both luminance and chromatic polarity were mismatched (−Lum−Chr), thresholds were substantially elevated under all conditions. With the same luminance contrast polarity and opposite chromatic polarity (+Lum−Chr) thresholds were only elevated close to isoluminance; in the reverse condition (−Lum+Chr), thresholds were elevated as in the −Lum−Chr condition except close to equiluminance. Similar data were obtained for gratings isolating the short-wavelength cone mechanism. Further psychophysical measurements assessed the role of target separation with matched or mismatched contrast polarity; similar results were found for luminance and chromatic gratings. Comparison physiological data were collected from parafoveal ganglion cells of the macaque retina. Positional precision of ganglion cell signals was assessed under conditions related to the psychophysical measurements. On the basis of these combined observations, it is argued that both magnocellular, parvocellular, and koniocellular pathways have access to cortical positional mechanisms associated with vernier acuity. [Copyright &y& Elsevier]

Achromatic visual function in primates is distributed between two pathways from retina to cortex, the parvocellular and the magnocellular. The relative contribution of these to human achromatic vision is controversial and largely unknown. Here, we use an optic neuritis (ON) model to investigate the effects of a severe loss of parvocellular function on human contrast sensitivity. In our first experiment, we use Gabor stimuli (0.5 cpd, 2 Hz) to show that, compared to normal control eyes, ON causes selective deficits in the two chromatic, cone opponent pathways, with L/M cone opponency affected more than S cone opponency, and a relative sparing of achromatic function. Since L/M cone opponency is carried exclusively by the midget ganglion cells of the parvocellular pathway, this demonstrates a selective deficit of parvocellular function. In a second experiment, we report on two subjects who have lost all L/M cone opponent response in both eyes, indicating a severe loss of parvocellular function. We measure the spatial and temporal contrast sensitivity functions of their remaining achromatic vision, compared with a normal control group, to determine the selectivity of the visual deficit caused by the differential parvocellular loss, and assess the relative contributions of the parvocellular and magnocellular pathways to achromatic contrast sensitivity. We find that parvocellular function contributes selectively at mid- to high spatial frequencies (at low temporal frequencies), whereas magnocellular function determines contrast sensitivity over a very broad temporal frequency range (at low spatial frequencies). Our data bear a striking resemblance to results obtained from primate parvocellular lesions. [ABSTRACT FROM AUTHOR]

Fragile X syndrome is the most common cause of inherited intellectual impairment and the most common single-gene cause of autism. Individuals with fragile X syndrome present with a neurobehavioural phenotype that includes selective deficits in spatiotemporal visual perception associated with neural processing in frontal–parietal networks of the brain. The goal of the current study was to examine whether reduced resolution of spatial and/or temporal visual attention may underlie perceptual deficits related to fragile X syndrome. Eye tracking was used to psychophysically measure the limits of spatial and temporal attention in infants with fragile X syndrome and age-matched neurotypically developing infants. Results from these experiments revealed that infants with fragile X syndrome experience drastically reduced resolution of temporal attention in a genetic dose-sensitive manner, but have a spatial resolution of attention that is not impaired. Coarse temporal attention could have significant knock-on effects for the development of perceptual, cognitive and motor abilities in individuals with the disorder. [ABSTRACT FROM AUTHOR]

Abstract: Fragile X syndrome (FXS) is characterized by the impairment of the magnocellular/dorsal visual system. In this study, we explored how fragile X protein (FMRP) expression may affect visual functions in healthy participants. The percentage of FMRP-positive lymphocytes was measured using a rapid antibody test in blood smears of 100 male volunteers. CGG triplet expansion was also determined. Results revealed that participants with fewer FMRP-positive lymphocytes exhibited lower performances on tests biasing information processing toward the magnocellular pathway and dorsal visual stream (contrast sensitivity at low spatial/high temporal frequency and motion coherence). It was not observed in the case of tests biasing information processing toward the parvocellular pathway and ventral stream (contrast sensitivity at high spatial/low temporal frequency and form coherence). These results suggest that healthy persons with lower peripheral FMRP expression display a visual phenotype similar to that described in patients with FXS. [Copyright &y& Elsevier]

Abstract: Regions of visual texture can be automatically segregated from one another when they abut but also discriminated from one another if they are separated in space or time. A difference in mean orientation between two textures serves to facilitate their segmentation, whereas a difference in orientation variance does not. The present study further supports this notion, by replicating the findings of in showing that judgments (odd-one-out) made for textures that differ in mean orientation were more accurate (and more rapid) when the textures were abutting than when separated, whereas judgments of variance were made no more accurately for abutting relative to separated textures. Interestingly, however, responses were overall faster for textures differing in variance when they were separated compared to when they were abutting. This is perhaps due to the clear separation boundary, which serves to delineate the regions on which to perform some regional estimation of orientation variance. A second experiment highlights the phase-insensitivity of texture segmentation, in that locating a texture edge (defined by a difference in mean orientation) in high frequency orientation-reversing stimuli can be performed at much higher frequencies than the discrimination of the same regions but with the texture contour masked. Textures that differed in variance did not exhibit this effect. A final experiment demonstrates that the phase-insensitive perception of texture borders improves with eccentric viewing relative to the fovea, whereas perception of the texture regions does not. Together, these experiments show dissociations between edge- and region-based texture analysis mechanisms and suggest a fast, sign-invariant contour extraction system mediating texture segmentation, which may be closely linked to the magnocellular subdivision of visual processing. [Copyright &y& Elsevier]

Purpose. This study examined the effects of Direction Discrimination Training (DDT) on reading performance in dyslexics. In particular, the study examined whether increasing stimulus complexity and the amount of training would increase reading fluency more than in previous studies, as well as whether these improvements were sustained over time. Methods: DDT, using patterns that maximally activate magnocellular neurons, was administered to dyslexic children over the same amount of time (3 months) for twice the frequency each week, using twice as many stimulus complexity levels, as administered in previous studies. A computer-based reading speed task followed DDT to provide reading practice. In addition, the results from the same dyslexics in two previous studies were reanalyzed to determine whether the improvements in reading fluency following DDT in second grade were retained and manifest in third grade. Results: Contrast sensitivity for direction discrimination increased significantly over that found previously. Reading rates improved 11 fold, in contrast to previous studies of DDT over the same length of time, which found that reading rates improved only 4 fold. Not only did reading fluency improve when dyslexics were trained to discriminate the direction of motion at low contrasts, but spelling, word identification, and comprehension also improved 1-3 grade levels. These improvements persisted over time. Conclusions: These results suggest that improving the timing and sensitivity of the direction selective cells is linked to improving reading performance. DDT appears to improve magnocellular function in the dorsal stream which may be essential for guiding the attention gateway. The data suggest that it tunes visual neural timing in the dorsal stream, enabling it to guide the ventral stream, improving reading skills, as well as figure/ground discrimination, attention, and processing speed. Our data indicates that this program provides a comprehensive, rapid, and effective regimen for remediating reading problems. [ABSTRACT FROM AUTHOR]

Vision therapy involves the use of lenses, prisms, filters and instrumentation to effect change in the neurological pathways that direct our visual system. Prisms of moderate to high power can have powerful effects on this neurology and should be considered primary tools in the therapy room. Prisms and lenses have optical, perceptual, and visual properties that make them unique in the effects they are able to create. This makes them a valuable tool in the vision therapy room. This paper will explore the rationale behind prism-based therapy procedures and uses procedure examples to help the reader integrate prisms into their therapy routine. [ABSTRACT FROM AUTHOR]

link between affect and action has been supported by the discovery that threat information is prioritized through an action-centred pathway-the dorsal visual stream. Magnocellular afferents, which originate from the retina and project to dorsal stream structures, are suppressed by exposure to diffuse red light, which diminishes humans' perception of threat-based images. In order to explore the role of colour in the relationship between affect and action, participants donned different pairs of coloured glasses (red, yellow, green, blue and clear) and completed Positive and Negative Affect Scale questionnaires as well as a series of target-directed aiming movements. Analyses of affect scores revealed a significant main effect for affect valence and a significant interaction between colour and valence: perceived positive affect was significantly smaller for the red condition. Kinematic analyses of variable error in the primary movement direction and Pearson correlation analyses between the displacements travelled prior to and following peak velocity indicated reduced accuracy and application of online control processes while wearing red glasses. Variable error of aiming was also positively and significantly correlated with negative affect scores under the red condition. These results suggest that only red light modulates the affect-action link by suppressing magnocellular activity, which disrupts visual processing for movement control. Furthermore, previous research examining the effect of the colour red on psychomotor tasks and perceptual acceleration of threat-based imagery suggest that stimulus-driven motor performance tasks requiring online control may be particularly susceptible to this effect. [ABSTRACT FROM AUTHOR]

Abstract: The experiments conducted aimed to investigate whether reduced accuracy when counting stimuli presented in rapid temporal sequence in adults with dyslexia could be explained by a sensory processing deficit, a general slowing in processing speed or difficulties shifting attention between stimuli. To achieve these aims, the influence of the inter-stimulus interval (ISI), stimulus duration, and sequence length were evaluated in two experiments. In the first that used skilled readers only, significantly more errors were found with presentation of long sequences when the ISI or stimulus durations were short. Experiment 2 used a wider range of ISIs and stimulus durations. Compared to skilled readers, a group with dyslexia had reduced accuracy on two-stimulus sequences when the ISI was short, but not when the ISI was long. Although reduced accuracy was found on all short and long sequences by the group with dyslexia, when performance on two-stimulus sequences was used as an index of sensory processing efficiency and controlled, group differences were found with presentation of stimuli of short duration only. We concluded that continuous, repetitive stimulation to the same visual area can produce a capacity limitation on rapid counting tasks in all readers when the ISIs or stimulus durations are short. While reduced accuracy on rapid sequential counting tasks can be explained by a sensory processing deficit when the stimulus duration is long, slower processing speed in the group with dyslexia explains the greater inaccuracy found as sequence length is increased when the stimulus duration is short. [Copyright &y& Elsevier]

Schizophrenia, it has been hypothesized, is linked to a deficiency in the magnocellular portion of the visual system. Abnormal backward masking has been invoked as support for this hypothesis. The rationale for linking backward masking to the magnocellular system is the hypothesis that fast responses in the magnocellular systems catches up with, and then inhibits slower responses in the parvocellular system. However, the latency difference between the magno- and parvocellular systems is at most 20 ms. Magnocellular abnormalities as a result would be expected to manifest themselves only at relatively short stimulus onset asynchronies (SOAs) or interstimulus intervals (ISIs). The present study examines this implication. It is found that a substantial number of investigations have uncovered abnormal masking at SOAs or ISIs of 300 ms or larger, and some even at ISIs as large as 700 ms. It is difficult to reconcile abnormalities at these SOAs and ISIs with magno-parvocellular latency differences of 20 ms or less. It is concluded that the abnormal masking does not support the existence of a magnocellular deficiency in schizophrenia. [ABSTRACT FROM AUTHOR]

It has been proposed that magnocellular and parvocellular sensitivity in schizophrenic individuals can be assessed using steady-state visually evoked potentials (VEPs) to either low-contrast stimuli or stimuli whose contrast is modulated around a high contrast “pedestal” (Green MF, Butler PD, Chen Y, et al. Schizophr Bull. 2009;35:163–181). This suggestion faces 2 difficulties: (1) To use low-contrast stimuli to activate the magnocellular system is inconsistent with lesion studies that have shown that under many conditions, the parvocellular system responds to the lowest contrasts and (2) To rely on contrast-response relationships to identify magnocellular and parvocellular responses is difficult because other neurons exist in the visual system that have contrast-response relationships similar to those of magnocellular and parvocellular cells. [ABSTRACT FROM PUBLISHER]