The shape-frequency and shape-amplitude after-effects, or SFAE and SAAE, refer respectively to the shifts observed in the perceived shape-frequency and shape-amplitude of a sinusoidal test contour following adaptation to a similar-shaped contour. As with other shape after-effects the shifts are in a direction away from that of the adapting stimulus. Using a variety of procedures we tested whether the spatial feature that was adapted in the SFAE and SAAE was (a) local orientation, (b) average unsigned curvature, (c) periodicity/density, (d) shape-amplitude and (e) local curvature. Our results suggest that the last of these, local curvature, underlies both the SFAE and SAAE. The evidence in favour of local curvature was that the after-effect reached its maximum value when just half-a-cycle of the test contour, in +/-cosine phase, was present. We suggest that the SFAE and SAAE are mediated by intermediate-level mechanisms that encode the shapes of contour fragments with constant sign of curvature. Given the neurophysiological evidence that neurons in area V4 encode parts of shapes with constant sign of curvature, we suggest V4 is the likely neural substrate for both the SFAE and SAAE.

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 selective.

Electrophysiological studies of symmetry have found a difference wave termed the Sustained Posterior Negativity (SPN) related to the presence of symmetry. Yet the extent to which the SPN is modulated by luminance-polarity and colour content is unknown. Here we examine how luminance-polarity distribution across the symmetry axis, grouping by luminance polarity, and the number of colours in the stimuli, modulate the SPN. Stimuli were dot patterns arranged either symmetrically or quasi-randomly. There were several arrangements: ’segregated’-symmetric dots were of one polarity and randomly-positioned dots were of the other; ‘unsegregated’-symmetric dots were of both polarities in equal proportions; ‘anti-symmetric’-dots were of opposite polarity across the symmetry axis; ‘polarity-grouped anti-symmetric’-this is the same as anti-symmetric but with half the pattern of one polarity and the other half of opposite polarity; multi-colour symmetric patterns made of two, three to four colours. We found that the SPN is: (i) reduced by the amount of position-symmetry, (ii) sensitive to luminance-polarity mismatch across the symmetry axis, and (iii) not modulated by the number of colours in the stimuli. Our results show that the sustained nature of the SPN coincides with the late onset of a topographic microstate sensitive to symmetry. These findings emphasise the importance of not only position symmetry, but also luminance polarity matching across the symmetry axis.

The human visual system has specialised mechanisms for encoding mirror-symmetry and for detecting symmetric motion-directions for objects that loom or recede from the observers. The contribution of motion to mirror-symmetry perception has never been investigated. Here we examine symmetry detection thresholds for stationary (static and dynamic flicker) and symmetrically moving patterns (inwards, outwards, random directions) with and without positional symmetry. We also measured motion detection and direction-discrimination thresholds for horizontal (left, right) and symmetrically moving patterns with and without positional symmetry. We found that symmetry detection thresholds were (a) significantly higher for static patterns, but there was no difference between the dynamic flicker and symmetrical motion conditions, and (b) higher than motion detection and direction-discrimination thresholds for horizontal or symmetrical motion, with or without positional symmetry. In addition, symmetrical motion was as easy to detect or discriminate as horizontal motion. We conclude that whilst symmetrical motion per se does not contribute to symmetry perception, limiting the lifetime of pattern elements does improve performance by increasing the number of element-locations as elements move from one location to the next. This may be explained by a temporal integration process in which weak, noisy symmetry signals are combined to produce a stronger signal.

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.

Contextual modulation refers to the effect of texture placed outside of a neuron's classical receptive field as well as the effect of surround texture on the perceptual properties of variegated regions within. In this minireview, we argue that one role of contextual modulation is to enhance the perception of contours at the expense of textures, in short to de-texturize the image. The evidence for this role comes mainly from three sources: psychophysical studies of shape after-effects, computational models of neurons that exhibit iso-orientation surround inhibition, and fMRI studies revealing specialized areas for contour as opposed to texture processing. The relationship between psychophysical studies that support the notion of contextual modulation as de-texturizer and those that investigate contour integration and crowding is discussed.

We investigated the first-order inputs to contour-shape mechanisms using the shape-frequency after-effect (SFAE), in which adaptation to a sinusoidally modulated contour causes a shift in the apparent shape-frequency of a test contour in a direction away from that of the adapting stimulus [Kingdom F. A. A., & Prins N. (2005a). Different mechanisms encode the shapes of contours and contour-textures. Journal of Vision 5(8), 463, (Abstract)]. We measured SFAEs for adapting and test contours (and edges) that differed in the contrast-polarity, scale (or blur) and magnitude of luminance contrast. The rationale was that if the SFAE was found to be reduced when adaptor and test differed along a particular dimension of luminance contrast, contour-shape mechanisms must be tuned to that dimension. Our results reveal that SFAEs manifest (i) a degree of selectivity to luminance contrast polarity for both even-symmetric (contours only) and odd-symmetric (both contours and edges) luminance profiles; (ii) a degree of selectivity to luminance scale (or blur); (iii) higher selectivity to fine compared to coarse scale for broadband edges (iv) a small preference for equal-in-contrast adaptors and tests. These results suggest that contour shapes are not encoded in the form of a sparse, cartoon-like sketch, as might be presumed by local energy (i.e. non-phase-selective) or form-cue invariant models, but instead in a form that is relatively 'feature-rich.'

The shape-frequency and shape-amplitude after-effects, or SFAE and SAAE, are phenomena in which adaptation to a sinusoidal-shaped contour results in a shift in, respectively, the perceived shape-frequency and perceived shape-amplitude of a test contour in a direction away from that of the adapting stimulus. Recent evidence shows that the SFAE and SAAE are mediated by mechanisms sensitive to curvature [Gheorghiu, E., & Kingdom, F. A. A. (2007a). The spatial feature underlying the shape-frequency and shape-amplitude after-effects. Vision Research, 47(6), 834-844]. Therefore we have used the SFAE and SAAE as a tool to study curvature processing. We examined whether curvature-encoding mechanisms are selective for (i) shape-phase, (ii) curvature polarity (or sign) and (iii) local orientation. We also investigated whether (iv) the two orthogonal dimensions of a curve, the sag and the cord, are encoded independently, and (v) whether curvature encoders are organized in an opponent manner. SFAEs/SAAEs were measured for adapting and test contours that differed or not in a given spatial property, the rationale being that if the after-effects were smaller when adaptor and test differed in a particular spatial property then curvature-encoding mechanisms must be selective for that spatial property. Our results reveal that SFAEs and SAAEs show (i) a degree of selectivity to curves that are mirror symmetric (in our stimuli half-cycle sine-wave contours in cosine (0/180deg) shape-phase); (ii) a degree of selectivity to the sign or polarity of curvature; (iii) a degree of selectivity to local orientation; (iv) independent coding of the sag and the cord of the curve, and (v) no evidence for opponent-curvature coding. The results agree with neurophysiological studies showing that simple shape dimensions are encoded independently.