Widespread deficits are known to accompany normal aging. Contrast thresholds of older and younger observers were measured for static and drifting gratings defined by luminance (first-order) or by contrast (second-order), and for a temporally segmented second-order motion stimulus. Results showed that older individuals had a larger threshold elevation for the perception of second-order stimuli than for the perception of first-order stimuli. This suggests a dissociation between the mechanisms underlying the perception of first and second-order stimuli, and demonstrates that aging may affect the more numerous processing steps required for the analysis of higher level stimuli.

Detection thresholds for radial deformations of circular contours were measured using a range of radii and contour peak spatial frequencies. For radial frequencies above two cycles, thresholds were found to be a constant fraction of the mean radius across a four-octave range of pattern radii and peak spatial frequencies (mean Weber fraction: 0.003-0.004). At low radial frequencies, thresholds were unaffected by contrast reduction. In 167 ms presentations, subjects were able to identify radial frequencies of six cycles and below with an accuracy of over 90% correct even when phase was randomized. The extreme sensitivity of subjects to these radial deformations (as low as 2-4 s of arc) cannot be explained by local orientation or curvature analysis, and points instead to the global pooling of contour information at intermediate levels of form vision.

Healthy human aging can have adverse effects on cortical function and on the brain's ability to integrate visual information to form complex representations. Facial identification is crucial to successful social discourse, and yet, it remains unclear whether the neuronal mechanisms underlying face perception per se, and the speed with which they process information, change with age. We present face images whose discrimination relies strictly on the shape and geometry of a face at various stimulus durations. Interestingly, we demonstrate that facial identity matching is maintained with age when faces are shown in the same view (e.g., front-front or side-side), regardless of exposure duration, but degrades when faces are shown in different views (e.g., front and turned 20 degrees to the side) and does not improve at longer durations. Our results indicate that perceptual processing speed for complex representations and the mechanisms underlying same-view facial identity discrimination are maintained with age. In contrast, information is degraded in the neural transformations that represent facial identity across views. We suggest that the accumulation of useful information over time to refine a representation within a population of neurons saturates earlier in the aging visual system than it does in the younger system and contributes to the age-related deterioration of face discrimination across views.

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In the primate visual system relatively complex patterns such as curved shapes are first represented at intermediate levels of the ventral pathway. Furthermore, there is now evidence for the existence of curvature population coding in primate V4. We sought to determine whether similar encoding occurs in the human visual system by using a context-dependent lateral masking paradigm. In this paradigm a central closed contour comprising the test pattern is masked by surrounding larger or smaller patterns with various configurations. Results indicate that test thresholds are not affected by a circular control mask, and that elevations are greatest when curvature extrema of the mask are aligned with those of the target. These lateral interactions extend over greater than 1 degrees and are tuned for target shape. Masking increases with the number of local curvature extrema aligned with the target. Finally, masking persists when target and mask have orthogonal local orientations and increases with mask amplitude. These findings are incompatible with local orientation-selective interactions (V1-mediated) but are consistent with the existence of population codes based on curvature maxima at intermediate levels of processing (presumably V4) in human vision. The paradigm we introduce provides a new tool for evaluating the representation of complex percepts.

We investigated the neural correlates of facial processing changes in healthy aging using fMRI and an adaptation paradigm. In the scanner, participants were successively presented with faces that varied in identity, viewpoint, both, or neither and performed a head size detection task independent of identity or viewpoint. In right fusiform face area (FFA), older adults failed to show adaptation to the same face repeatedly presented in the same view, which elicited the most adaptation in young adults. We also performed a multivariate analysis to examine correlations between whole-brain activation patterns and behavioral performance in a face-matching task tested outside the scanner. Despite poor neural adaptation in right FFA, high-performing older adults engaged the same face-processing network as high-performing young adults across conditions, except the one presenting a same facial identity across different viewpoints. Low-performing older adults used this network to a lesser extent. Additionally, high-performing older adults uniquely recruited a set of areas related to better performance across all conditions, indicating age-specific involvement of this added network. This network did not include the core ventral face-processing areas but involved the left inferior occipital gyrus, frontal, and parietal regions. Although our adaptation results show that the neuronal representations of the core face-preferring areas become less selective with age, our multivariate analysis indicates that older adults utilize a distinct network of regions associated with better face matching performance, suggesting that engaging this network may compensate for deficiencies in ventral face processing regions.

Mechanisms selective for complex shape are vulnerable to adaptation techniques historically used to probe those underlying performance in lower-level visual tasks. We explored the nature of these shape after-effects using radial frequency patterns. Adapting to a radial frequency pattern resulted in a strong and systematic after-effect of a pattern that was 180 degrees out of phase with the adapting pattern. This after-effect was characterized as both a shift in the point of subjective equality and an increase in response uncertainty. The after-effect transferred across adapting pattern contrast and adaptor amplitude, suggesting an involvement from shape-specific mechanisms located at higher processing stages along the visual pathway. Moreover, our results suggested that the shift in the point of subjective equality was guided by global processing mechanisms, whereas the increase in uncertainty reflected activity from local processing mechanisms. Together, these results suggest that shape-specific after-effects reflect gain control processes at various stages of processing along the ventral pathway.

No abstract