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Postadaptation orientation discrimination
Abstract
An orientational difference of only 0.3–0.5 deg can be discriminated between two gratings or two lines, although psychophysical channels and cortical cells both have comparatively broad orientation bandwidths of 10–25 deg. One proposed explanation for the fineness of orientation discrimination is that, while detection is determined by the most excited orientation-tuned neural elements, superthreshold orientation discrimination is determined by difference signals between these elements [ Westheimer, J. Opt. Soc. Am.66, 332 ( 1976)]. This implies that, if stimulus orientation is changed slightly, the most important elements for discriminating this change will be those whose relative activity changes most, even though the excitation of these elements may be comparatively weak. In accord with this prediction, we found that adapting to a high-contrast grating degraded discrimination for test gratings inclined at about 10–20 deg to the adapting grating while having little effect on the detection of these inclined gratings. For test gratings parallel to the adapting grating, discrimination was improved, but detection was degraded. Either an opponent-process or a line-element model can account for these effects of adaptation. An opponent model can also explain our findings that subjects do not confound orientation change with contrast change and that suprathreshold orientation discrimination is almost independent of contrast, varying by only ±10% from about 3 to about 25 times contrast threshold. A discrimination model must incorporate reliable storage of spatial frequency, because discrimination was not affected by increasing the interval between grating presentations from 1 to 10 sec. In spatial form vision the relation between postadaptation detection and discrimination is formally similar along the dimensions of orientation and of size, and these two independent spatial discriminations can be modeled in formally similar ways, for example, in terms of orientation opponency and size opponency among multiple local elements, each of which is tuned to a different orientation and/or size.
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Citations
Cites
Orientation selectivity in the cat's striate cortex is invariant with stimulus contrast
Sclar, G., & Freeman, R. D. (1982) · Experimental Brain Research · doi:10.1007/bf00238641 · Cited by 339
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Hickok, G. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3158 · Cited by 837
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Gutnisky, D. A., & Dragoi, V. (2008) · Nature · doi:10.1038/nature06563 · Cited by 337
Not Noisy, Just Wrong: The Role of Suboptimal Inference in Behavioral Variability
Beck, J. M., Ma, W. J., Pitkow, X., Latham, P. E., & Pouget, A. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.016 · Cited by 316
Physiological Correlates of Perceptual Learning in Monkey V1 and V2
Ghose, G. M., Yang, T., & Maunsell, J. H. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00690.2001 · Cited by 310
Metadata
- Authors
- Regan, D., & Beverley, K. I.
- Venue
- Journal of the Optical Society of America A
- Publisher
- Optica Publishing Group
- Published
- 1985-02-01
- Volume
- 2
- Issue
- 2
- Pages
- 147
- ISSN
- 1084-7529 (ISSN-L)
- 1520-8532
- OpenAlex
- W2044266503
- Cited by
- 404
- References
- 1
- FWCI
- 17.59
- Type
- journal article
- Language
- en
- Open access
- closed
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- Regan, D., & Beverley, K. I. (1985). Postadaptation orientation discrimination. Journal of the Optical Society of America A. https://doi.org/10.1364/josaa.2.000147
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