Further Examination of the Pulsed- and Steady-Pedestal Paradigms under Hypothetical Parvocellular- and Magnocellular-Biased Conditions.

The pulsed- and steady-pedestal paradigms were designed to track increment thresholds (Δ) as a function of pedestal contrast (C) for the parvocellular (P) and magnocellular (M) systems, respectively. These paradigms produce contrasting results: linear relationships between Δ and are observed in the pulsed-pedestal paradigm, indicative of the P system's processing, while the steady-pedestal paradigm reveals nonlinear functions, characteristic of the M system's response. However, we recently found the P model fits better than the M model for both paradigms, using Gabor stimuli biased towards the M or P systems based on their sensitivity to color and spatial frequency.

Examining Increment thresholds as a function of pedestal contrast under hypothetical parvo- and magnocellular-biased conditions.

Theoretically, the pulsed- and steady-pedestal paradigms are thought to track contrast-increment thresholds (ΔC) as a function of pedestal contrast (C) for the parvocellular (P) and magnocellular (M) systems, respectively, yielding linear ΔC versus C functions for the pulsed- and nonlinear functions for the steady-pedestal paradigm. A recent study utilizing these paradigms to isolate the P and M systems reported no evidence of the M system being suppressed by red light, contrary to previous physiological and psychophysical findings. Curious as to why this may have occurred, we examined how ΔC varies with C for the P and M systems using the pulsed- and steady-pedestal paradigms and stimuli biased towards the P or M systems based on their sensitivity to spatial frequency (SF) and color.

Visual Memory Scan Slopes: Their Changes over the First Two Seconds of Processing.

Using the prime-probe comparison paradigm, Jacob, Breitmeyer, and Treviño (2013) demonstrated that information processing in visual short-term memory (VSTM) proceeds through three stages: sensory visible persistence (SVP), nonvisible informational persistence (NIP), and visual working memory (VWM). To investigate the effect of increasing the memory load on these stages by using 1, 3, and 5 display items, measures of VSTM performance, including storage, storage-slopes, and scan-slopes, were obtained. Results again revealed three stages of VSTM processing, but with the NIP stage increasing in duration as memory load increased, suggesting a need, during the NIP stage, for transfer and encoding delays of information into VWM.

Interactions between visual working memory and visual attention among survivors of pediatric acute lymphoblastic leukemia (ALL) and their healthy peers.

: There is increasing concern for adverse cognitive late effects among survivors of pediatric acute lymphoblastic leukemia (ALL) given the widespread impact they have on academic achievement, particularly working memory and attention. We assessed performance among survivors and their healthy peers on a dual task paradigm measuring visual working memory (VWM) and visual attention independently and the dynamic relationship between the two. Assessing specific subsets within cognitive domains allows for understanding the distinct nature of cognitive impairments.

Contrast sensitivity indicates processing level of visual illusions.

A nearly linear contrast response function (CRF) is found in the lower level striate cortex whereas a steep, nonlinear increase at lower contrasts that gradually increases toward response saturation for higher contrasts is found in the higher level extrastriate cortex. This change of CRFs along the ventral cortical pathway indicates a shift from stimulus- and energy-dependent coding at lower levels to percept- and information-dependent coding at higher levels. The increase of nonlinearity at higher levels optimizes the extraction of perceptual information by amplifying responses to the ubiquitous low-contrast inputs in the environment.

Can Contrast-Response Functions Indicate Visual Processing Levels?

Many visual effects are believed to be processed at several functional and anatomical levels of cortical processing. Determining if and how the levels contribute differentially to these effects is a leading problem in visual perception and visual neuroscience. We review and analyze a combination of extant psychophysical findings in the context of neurophysiological and brain-imaging results.

Psychophysical "blinding" methods reveal a functional hierarchy of unconscious visual processing.

Numerous non-invasive experimental "blinding" methods exist for suppressing the phenomenal awareness of visual stimuli. Not all of these suppressive methods occur at, and thus index, the same level of unconscious visual processing. This suggests that a functional hierarchy of unconscious visual processing can in principle be established.

Exploring facial emotion perception in schizophrenia using transcranial magnetic stimulation and spatial filtering.

Schizophrenia patients have difficulty extracting emotional information from facial expressions. Perception of facial emotion can be examined by systematically altering the spatial frequency of stimuli and suppressing visual processing with temporal precision using transcranial magnetic stimulation (TMS). In the present study, we compared 25 schizophrenia patients and 27 healthy controls using a facial emotion identification task.

Contributions of magno- and parvocellular channels to conscious and non-conscious vision.

The dorsal and ventral cortical pathways, driven predominantly by magnocellular (M) and parvocellular (P) inputs, respectively, assume leading roles in models of visual information processing. Although in prior proposals, the dorsal and ventral pathways support non-conscious and conscious vision, respectively, recent modelling and empirical developments indicate that each pathway plays important roles in both non-conscious and conscious vision. In these models, the ventral P-pathway consists of one subpathway processing an object's contour features, e.

Tracking the first two seconds: three stages of visual information processing?

We compared visual priming and comparison tasks to assess information processing of a stimulus during the first 2 s after its onset. In both tasks, a 13-ms prime was followed at varying SOAs by a 40-ms probe. In the priming task, observers identified the probe as rapidly and accurately as possible; in the comparison task, observers determined as rapidly and accurately as possible whether or not the probe and prime were identical.

Assessing temporal processing of facial emotion perception with transcranial magnetic stimulation.

The ability to process facial expressions can be modified by altering the spatial frequency of the stimuli, an effect that has been attributed to differential properties of visual pathways that convey different types of information to distinct brain regions at different speeds. While this effect suggests a potential influence of spatial frequency on the processing speed of facial emotion, this hypothesis has not been examined directly. We addressed this question using a facial emotion identification task with photographs containing either high spatial frequency (HSF), low spatial frequency (LSF), or broadband spatial frequency (BSF).

Object substitution masking in schizophrenia: an event-related potential analysis.

Schizophrenia patients exhibit deficits on visual processing tasks, including visual backward masking, and these impairments are related to deficits in higher-level processes. In the current study we used electroencephalography techniques to examine successive stages and pathways of visual processing in a specialized masking paradigm, four-dot masking, which involves masking by object substitution. Seventy-six schizophrenia patients and 66 healthy controls had event-related potentials (ERPs) recorded during four-dot masking.

Spatial attention effects during conscious and nonconscious processing of visual features and objects.

Flanker congruency effects were measured in a masked flanker task to assess the properties of spatial attention during conscious and nonconscious processing of form, color, and conjunctions of these features. We found that (1) consciously and nonconsciously processed colored shape distractors (i.e.

Nonconscious and conscious color priming in schizophrenia.

Deficits in visual processing are well established in schizophrenia. However, there is conflicting evidence about whether these deficits start before the formation of percepts because visual processing studies in schizophrenia have typically examined the processing of consciously registered stimuli. In this study, we used nonconscious color priming to evaluate the very early visual processing stages in schizophrenia.

Roles of contour and surface processing in microgenesis of object perception and visual consciousness.

Developments in visual neuroscience and neural-network modeling indicate the existence of separate pathways for the processing of form and surface attributes of a visual object. In line with prior theoretical proposals, it is assumed that the processing of form can be explicit or conscious only as or after the surface property such as color is filled in. In conjunction with extant psychophysical findings, these developments point to interesting distinctions between nonconscious and conscious processing of these attributes, specifically in relation to distinguishable temporal dynamics.

Microgenesis of surface completion in visual objects: evidence for filling-out.

Using metacontrast masking we examined the temporal dynamics of surface completion in object vision. By varying the stimulus onset asynchrony between the target object and the flanking mask(s), we obtained estimates of the time required for the entire surface contrast to fill out within the area delimited by the contours/edges of the target. The estimated speed of the filling-out process was 36.

Metacontrast masking with texture-defined second-order stimuli.

We examine metacontrast masking with texture-defined second-order stimuli. Our results reveal that (1) the monotonic type A as well as the nonmonotonic (U-shaped) type B metacontrast effect, which has been extensively examined with first-order luminance-defined stimuli, can be obtained with texture-defined second-order stimuli; and (2) while variations of luminance contrast are known to affect the magnitude of metacontrast with first-order stimuli, neither the size nor orientation contrast between texture elements defining the second-order stimuli have a significant impact on the magnitude or shape of metacontrast. These findings bear on theories of metacontrast masking by showing that the mechanism giving rise to nonmonotonic masking effects can operate beyond the level of first-order stimulus processing.

Visual consciousness revisited: magnocellular and parvocellular contributions to conscious and nonconscious vision.

Current theoretical approaches to consciousness and vision associate the dorsal cortical pathway, in which magnocellular (M) input is dominant, with nonconscious visual processing and the ventral cortical pathway, in which parvocellular (P) input is dominant, with conscious visual processing. We explored the known differences between M and P contrast-response functions to investigate the roles of these channels in vision. Simulations of contrast-dependent priming revealed that priming effects obtained with unmasked, visible primes were best modeled by equations characteristic of M channel responses, whereas priming effects obtained with masked, invisible primes were best modeled by equations characteristic of P channel responses.

Metacontrast masking within and between visual channels: effects of orientation and spatial frequency contrasts.

We measured the strength and optimal target-mask onset asynchrony (SOA(max)) of metacontrast masking using Gabor patches as targets and sinusoidal rings with Gaussian envelopes as masks. We varied spatial frequencies (f) between 0.5 and 8 cpd to manipulate the degree to which spatial frequency channels in the visual system are triggered.

Properties of spatial attention in conscious and nonconscious visual information processing.

A modified flanker task was used to assess the effects of spatial attention during conscious and nonconscious processing. In line with prior findings, we demonstrated that increasing spatial separation between flankers and probes diminished the differences between reaction times to the incongruent and congruent probe-flanker pairs. This trend occurred even when the identity of flankers was suppressed from awareness by a metacontrast mask, indicating (1) that spatial attention can be allocated to information processed at the nonconscious, in addition to the conscious, levels, (2) that effects of spatial attention at these two levels can be equivalent, and (3) that attention deployed at the nonconscious level of processing can be characterized by a spatial gradient that is nearly identical to that found at the conscious level of processing.

Role of task-directed attention in nonconscious and conscious response priming by form and color.

Prior research on visual priming suggests that during nonconscious processing attention can be directed to single stimulus dimensions such as form or color. In the current experiment, nonconscious priming was compared to conscious priming by employing masking techniques that render primes invisible (masked) or visible (unmasked) to the observers. Observers were asked to respond to the form, the color, or the combination of form and color of the mask-probe that followed either a masked or an unmasked prime.