The Site of Size Constancy

Perception ◽  
1972 ◽  
Vol 1 (1) ◽  
pp. 111-119 ◽  
Author(s):  
C Blakemore ◽  
E T Garner ◽  
J A Sweet

Under appropriate conditions, with good depth cues, the perception of the bar width or spatial frequency of a pattern of black and white stripes (a grating) shows excellent size constancy. Two gratings at different distances look similar in spatial frequency when the actual width, not the angular width, of their stripes is the same. Adaptation to a high-contrast grating causes a rise in the threshold contrast for detecting gratings of similar orientation and spatial frequency. This aftereffect transfers from one eye to the other, so it probably depends on binocular orientation-selective neurones in the visual cortex. With the adapting grating at three times the distance of the test grating the maximum elevation of threshold occurs for exactly the same angular spatial frequency as that of the adapting pattern. Therefore the neural mechanism for size-constancy scaling probably occurs after the visual cortex, perhaps in the inferotemporal cortex.

2007 ◽  
Vol 98 (1) ◽  
pp. 187-195 ◽  
Author(s):  
Thang Duong ◽  
Ralph D. Freeman

Adaptation to a high-contrast grating stimulus causes reduced sensitivity to subsequent presentation of a visual stimulus with similar spatial characteristics. This behavioral finding has been attributed by neurophysiological studies to processes within the visual cortex. However, some evidence indicates that contrast adaptation phenomena are also found in early visual pathways. Adaptation effects have been reported in retina and lateral geniculation nucleus (LGN). It is possible that these early pathways could be the physiological origin of the cortical adaptation effect. To study this, we recorded from single neurons in the cat's LGN. We find that contrast adaptation in the LGN, unlike that in the visual cortex, is not spatial frequency specific, i.e., adaptation effects apply to a broad range of spatial frequencies. In addition, aside from the amplitude attenuation, the shape of spatial frequency tuning curves of LGN cells is not affected by contrast adaptation. Again, these findings are unlike those found for cells in the visual cortex. Together, these results demonstrate that pattern specific contrast adaptation is a cortical process.


1982 ◽  
Vol 55 (3_suppl) ◽  
pp. 1247-1256 ◽  
Author(s):  
Billie Salzman ◽  
Diane F. Halpern

The perceived depth associated with subjective contours was studied with a three-level subjective contour configuration. An analysis of subjects' size judgments showed significant size-constancy scaling consistent with the prediction that subjects would perceive the various subjective surfaces as superimposed upon one another in depth. Direct depth estimations, however, showed only weak depth effects, easily reversed by conflicting depth cues, and observed with real, as well as subjective contours. The discrepant results point to the possibility of different functional depth cues for the two tasks. The order of tasks, indicative of priming, further suggested that depth processing may be secondary to pattern recognition rather than being causal in the formation of subjective contours.


2010 ◽  
Vol 37 (7) ◽  
pp. 786-793 ◽  
Author(s):  
Liang SHI ◽  
Rui-Jie WU ◽  
Cui-Ping XU ◽  
Shou-Wen ZHANG ◽  
Hong-Wei ZHU ◽  
...  

2021 ◽  
pp. 095679762199520
Author(s):  
Nirit Fooks ◽  
Bat-Sheva Hadad ◽  
Orly Rubinsten

Although researchers have debated whether a core deficit of nonsymbolic representation of magnitude underlies developmental dyscalculia (DD), research has mostly focused on numerosity processing. We probed the possibility of a general magnitude deficit in individuals with DD and asked whether sensitivity to size varied in contexts of depth ordering and size constancy. We measured full psychometric functions in size-discrimination tasks in 12 participants with DD and 13 control participants. Results showed that although people with DD exhibited veridical perceived magnitude, their sensitivity to size was clearly impaired. In contrast, when objects were embedded in depth cues allowing size-constancy computations, participants with DD demonstrated typical sensitivity to size. These results demonstrate a deficit in the perceptual resolutions of magnitude in DD. At the same time, the finding of an intact size constancy suggests that when magnitude perception is facilitated by implicit mandatory computations of size constancy, this deficit is no longer evident.


2019 ◽  
Author(s):  
Marie Tolkiehn ◽  
Simon R. Schultz

AbstractOrientation tuning in mouse primary visual cortex (V1) has long been reported to have a random or “salt-and-pepper” organisation, lacking the structure found in cats and primates. Laminar in-vivo multi-electrode array recordings here reveal previously elusive structure in the representation of visual patterns in the mouse visual cortex, with temporo-nasally drifting gratings eliciting consistently highest neuronal responses across cortical layers and columns, whilst upward moving gratings reliably evoked the lowest activities. We suggest this bias in direction selectivity to be behaviourally relevant as objects moving into the visual field from the side or behind may pose a predatory threat to the mouse whereas upward moving objects do not. We found furthermore that direction preference and selectivity was affected by stimulus spatial frequency, and that spatial and directional tuning curves showed high signal correlations decreasing with distance between recording sites. In addition, we show that despite this bias in direction selectivity, it is possible to decode stimulus identity and that spatiotemporal features achieve higher accuracy in the decoding task whereas spike count or population counts are sufficient to decode spatial frequencies implying different encoding strategies.Significance statementWe show that temporo-nasally drifting gratings (i.e. opposite the normal visual flow during forward movement) reliably elicit the highest neural activity in mouse primary visual cortex, whereas upward moving gratings reliably evoke the lowest responses. This encoding may be highly behaviourally relevant, as objects approaching from the periphery may pose a threat (e.g. predators), whereas upward moving objects do not. This is a result at odds with the belief that mouse primary visual cortex is randomly organised. Further to this biased representation, we show that direction tuning depends on the underlying spatial frequency and that tuning preference is spatially correlated both across layers and columns and decreases with cortical distance, providing evidence for structural organisation in mouse primary visual cortex.


Author(s):  
David M. Arnoldussen ◽  
Jeroen Goossens ◽  
Albert V. van den Berg

Perception ◽  
1973 ◽  
Vol 2 (1) ◽  
pp. 53-60 ◽  
Author(s):  
J A Movshon ◽  
C Blakemore

An adaptation method is used to determine the orientation specificity of channels sensitive to different spatial frequencies in the human visual system. Comparison between different frequencies is made possible by a data transformation in which orientational effects are expressed in terms of equivalent contrast (the contrast of a vertical grating producing the same adaptational effect as a high-contrast grating of a given orientation). It is shown that, despite great variances in the range of orientations affected by adaptation at different spatial frequencies (±10° to ±50°), the half-width at half-amplitude of the orientation channels does not vary systematically as a function of spatial frequency over the range tested (2·5 to 20 cycles deg−1). Two subjects were used and they showed significantly different orientation tuning across the range of spatial frequencies. The results are discussed with reference to previous determinations of orientation specificity, and to related psychophysical and neurophysiological phenomena.


2012 ◽  
Vol 15 (12) ◽  
pp. 1683-1690 ◽  
Author(s):  
Ian Nauhaus ◽  
Kristina J Nielsen ◽  
Anita A Disney ◽  
Edward M Callaway

1973 ◽  
Vol 13 (7) ◽  
pp. 1255-1267 ◽  
Author(s):  
Lamberto Maffei ◽  
Adriana Fiorentini

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