Line Orientation Adaptation: Local or Global?

Prolonged exposure to an oriented line shifts the perceived orientation of a subsequently observed line in the opposite direction, a phenomenon known as the tilt aftereffect (TAE). Here we consider whether the TAE for line stimuli is mediated by a mechanism that integrates the local parts of the line into a single global entity prior to the site of adaptation, or the result of the sum of local TAEs acting separately on the parts of the line. To test between these two alternatives we used the fact the TAE transfers almost completely across luminance contrast polarity [1]. We measured the TAE using adaptor and test lines that (1) either alternated in luminance polarity or were of a single polarity, and (2) either alternated in local orientation or were of a single orientation. We reasoned that if the TAE was agnostic to luminance polarity and was parts-based, we should obtain large TAEs using alternating-polarity adaptors with single-polarity tests. However we found that (i) TAEs using one-alternating-polarity adaptors with all-white tests were relatively small, increased slightly for two-alternating-polarity adaptors, and were largest with all-white or all-black adaptors. (ii) however TAEs were relatively large when the test was one-alternating polarity, irrespective of the adaptor type. (iii) The results with orientation closely mirrored those obtained with polarity with the difference that the TAE transfer across orthogonal orientations was weak. Taken together, our results demonstrate that the TAE for lines is mediated by a global shape mechanism that integrates the parts of lines into whole prior to the site of orientation adaptation. The asymmetry in the magnitude of TAE depending on whether the alternating-polarity lines was the adaptor or test can be explained by an imbalance in the population of neurons sensitive to 1(st)-and 2(nd)-order lines, with the 2(nd)-order lines being encoded by a subset of the mechanisms sensitive to 1(st)-order lines.This research was supported by a Natural Sciences and Engineering Research Council of Canada (NSERC) grant #RGPIN 121713-11 given to FK and Australian Research Council grant DP110101511 to JB. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

Dichoptic difference thresholds for chromatic stimuli

We have investigated the properties of binocular color vision using a new measure: the Dichoptic Color Difference Threshold (DCDT). The DCDT is the smallest detectable difference in color between two dichoptically superimposed stimuli. DCDTs differ from conventional measures of binocular rivalry in that they are performance- not appearance-based. The dependency of DCDTs on (a) color direction and (b) color contrast was measured. The colors (chromaticities) of the stimuli were defined according to a scaled version of the MacLeod-Boynton color space, and the luminance and color contrasts of the stimulus pairs were equated using a matching procedure. DCDTs were measured using a forced-choice procedure in which subjects had to chose which of two stimuli had a between-eye-difference in color. DCDTs ranged from 9 degrees to 22 degrees of color angle depending on color direction. DCDTs were lower than binocular rivalry thresholds but higher than thresholds for discriminating the color pairs when placed side-by-side. There were no minima at either the cardinal color or unique hues directions, suggesting that DCDTs are not mediated by these mechanisms. DCDTs were however positively correlated with the measured perceived color difference between the color pairs when placed side-by-side

Dynamics of contextual modulation of perceived shape in human vision

In biological vision, contextual modulation refers to the influence of a surround pattern on either the perception of, or the neural responses to, a target pattern. One studied form of contextual modulation deals with the effect of a surround texture on the perceived shape of a contour, in the context of the phenomenon known as the shape aftereffect. In the shape aftereffect, prolonged viewing, or adaptation to a particular contour’s shape causes a shift in the perceived shape of a subsequently viewed contour. Shape aftereffects are suppressed when the adaptor contour is surrounded by a texture of similarly-shaped contours, a surprising result given that the surround contours are all potential adaptors. Here we determine the motion and temporal properties of this form of contextual modulation. We varied the relative motion directions, speeds and temporal phases between the central adaptor contour and the surround texture and measured for each manipulation the degree to which the shape aftereffect was suppressed. Results indicate that contextual modulation of shape processing is selective to motion direction, temporal frequency and temporal phase. These selectivities are consistent with one aim of vision being to segregate contours that define objects from those that form textured surfaces

Global shape processing involves feature-selective and feature-agnostic coding mechanisms

Recent research and modeling proposes that a closed shape is accurately described by both the curvature and angular location of its parts relative to the shape center, implying that the shape is coded along with its overall orientation.We tested this proposition. Radial frequency (RF) patterns were employed as stimuli as they can represent a range of familiar closed shapes and are processed globally. We measured a RF amplitude aftereffect (RFAAE) as a function of the shape orientation difference between adapt and test patterns of the same RF. For RF3 and RF4, RFAAEs were largest when adapt and test patterns were the same orientation, and then linearly decreased as the adaptor was rotated away from the test. RFAAEs did not, however, reach zero, instead plateauing significantly above zero. On the other hand, when adapt and test were of opposite luminance polarity, RFAAEs, although lower than same luminance-polarity RFAAEs, were invariant to differences between adapt and test orientations. Our findings provide evidence for two global shape mechanisms: one that is selective for shape orientation and luminance polarity, and one that is agnostic to these characteristics

Dichoptic difference thresholds for chromatic stimuli

a b s t r a c t We have investigated the properties of binocular color vision using a new measure: the Dichoptic Color Difference Threshold (DCDT). The DCDT is the smallest detectable difference in color between two dichoptically superimposed stimuli. DCDTs differ from conventional measures of binocular rivalry in that they are performance-not appearance-based. The dependency of DCDTs on (a) color direction and (b) color contrast was measured. The colors (chromaticities) of the stimuli were defined according to a scaled version of the MacLeod-Boynton color space, and the luminance and color contrasts of the stimulus pairs were equated using a matching procedure. DCDTs were measured using a forced-choice procedure in which subjects had to chose which of two stimuli had a between-eye-difference in color. DCDTs ranged from 9°to 22°of color angle depending on color direction. DCDTs were lower than binocular rivalry thresholds but higher than thresholds for discriminating the color pairs when placed side-by-side. There were no minima at either the cardinal color or unique hues directions, suggesting that DCDTs are not mediated by these mechanisms. DCDTs were however positively correlated with the measured perceived color difference between the color pairs when placed side-by-side

The role of color and attention-to-color in mirror-symmetry perception

The role of color in the visual perception of mirror-symmetry is controversial. Some reports support the existence of color-selective mirror-symmetry channels, others that mirror-symmetry perception is merely sensitive to color-correlations across the symmetry axis. Here we test between the two ideas. Stimuli consisted of colored Gaussian-blobs arranged either mirror-symmetrically or quasi-randomly. We used four arrangements: (1)‘segregated’ – symmetric blobs were of one color, random blobs of the other color(s); (2)‘random-segregated’ – as above but with the symmetric color randomly selected on each trial; (3)‘non-segregated’ – symmetric blobs were of all colors in equal proportions, as were the random blobs; (4)‘anti-symmetric’ – symmetric blobs were of opposite-color across the symmetry axis. We found: (a) near-chance levels for the anti-symmetric condition, suggesting that symmetry perception is sensitive to color-correlations across the symmetry axis; (b) similar performance for random-segregated and non-segregated conditions, giving no support to the idea that mirror-symmetry is color selective; (c) highest performance for the color-segregated condition, but only when the observer knew beforehand the symmetry color, suggesting that symmetry detection benefits from color-based attention. We conclude that mirror-symmetry detection mechanisms, while sensitive to color-correlations across the symmetry axis and subject to the benefits of attention-to-color, are not color selectiv

Global shape processing involves a hierarchy of integration stages. Vision Res

a b s t r a c t Radial Frequency (RF) patterns can be used to study the processing of familiar shapes, e.g. triangles and squares. Opinion is divided over whether the mechanisms that detect these shapes integrate local orientation and position information directly, or whether local orientations and positions are first combined to represent extended features, such as curves, and that it is local curvatures that the shape mechanism integrates. The latter view incorporates an intermediate processing stage, the former does not. To differentiate between these hypotheses we studied the processing of micro-patch sampled RF patterns as a function of the luminance polarity of successive elements on the contour path. Our first study measures shape after effects involving suprathreshold amplitude RF shapes and shows that alternating the luminance polarity of successive micro-patch elements disrupts adaptation of the global shape. Our second study shows that polarity alternations also disrupt sensitivity to threshold-amplitude RF patterns. These results suggest that neighbouring points of the contour shape are integrated into extended features by a polarity selective mechanism, prior to global shape processing, consistent with the view that for both threshold amplitude and suprathreshold amplitude patterns, global processing of RF shapes involves an intermediate stage of processing. Crow

Texture variations suppress suprathreshold brightness and colour variations

Discriminating material changes from illumination changes is a key function of early vision. Luminance cues are ambiguous in this regard, but can be disambiguated by co-incident changes in colour and texture. Thus, colour and texture are likely to be given greater prominence than luminance for object segmentation, and better segmentation should in turn produce stronger grouping. We sought to measure the relative strengths of combined luminance, colour and texture contrast using a suprathreshhold, psychophysical grouping task. Stimuli comprised diagonal grids of circular patches bordered by a thin black line and contained combinations of luminance decrements with either violet, red, or texture increments. There were two tasks. In the Separate task the different cues were presented separately in a two-interval design, and participants indicated which interval contained the stronger orientation structure. In the Combined task the cues were combined to produce competing orientation structure in a single image. Participants had to indicate which orientation, and therefore which cue was dominant. Thus we established the relative grouping strength of each cue pair presented separately, and compared this to their relative grouping strength when combined. In this way we observed suprathreshold interactions between cues and were able to assess cue dominance at ecologically relevant signal levels. Participants required significantly more luminance and colour compared to texture contrast in the Combined compared to Separate conditions (contrast ratios differed by about 0.1 log units), showing that suprathreshold texture dominates colour and luminance when the different cues are presented in combination

Maternal risk factors for abnormal placental growth: The national collaborative perinatal project

<p>Abstract</p> <p>Background</p> <p>Previous studies of maternal risk factors for abnormal placental growth have focused on placental weight and placental ratio as measures of placental growth. We sought to identify maternal risk factors for placental weight and two neglected dimensions of placental growth: placental thickness and chorionic plate area.</p> <p>Methods</p> <p>We conducted an analysis of 24,135 mother-placenta pairs enrolled in the National Collaborative Perinatal Project, a prospective cohort study of pregnancy and child health. We defined growth restriction as < 10^thpercentile and hypertrophy as > 90^thpercentile for three placental growth dimensions: placental weight, placental thickness and chorionic plate area. We constructed parallel multinomial logistic regression analyses to identify (a) predictors of restricted growth (vs. normal) and (b) predictors of hypertrophic growth (vs. normal).</p> <p>Results</p> <p>Black race was associated with an increased likelihood of growth restriction for placental weight, thickness and chorionic plate area, but was associated with a reduced likelihood of hypertrophy for these three placental growth dimensions. We observed an increased likelihood of growth restriction for placental weight and chorionic plate area among mothers with hypertensive disease at 24 weeks or beyond. Anemia was associated with a reduced likelihood of growth restriction for placental weight and chorionic plate area. Pre-pregnancy BMI and pregnancy weight gain were associated with a reduced likelihood of growth restriction and an increased likelihood of hypertrophy for all three dimensions of placental growth.</p> <p>Conclusion</p> <p>Maternal risk factors are either associated with placental growth restriction or placental hypertrophy not both. Our findings suggest that the placenta may have compensatory responses to certain maternal risk factors suggesting different underlying biological mechanisms.</p