Mirror symmetrical transfer of perceptual learning by prism adaptation

Vision Research

Volumn 47, Issue 10, 2007, Pages 1350-1361

  Tanaka, Yasuto ^a   Miyauchi, Satoru ^a   Misaki, Masaya ^a   Tashiro, Takara ^b  

^a NATIONAL INSTITUTE OF INFORMATION AND COMMUNICATIONS TECHNOLOGY   (Japan)

^b Osaka Prefecture University   (Japan)

Author keywords

Gabor lateral interaction; Mirror symmetry; Perceptual learning; Prism adaptation; Transfer

Indexed keywords

ARTICLE; CONTROLLED STUDY; HUMAN; HUMAN EXPERIMENT; LEARNING; PERCEPTION; PRIORITY JOURNAL; PRISM; RETINA IMAGE; VISUAL ADAPTATION; VISUAL CORTEX; VISUAL FIELD; VISUAL NERVOUS SYSTEM; VISUAL ORIENTATION;

ADAPTATION, OCULAR; ADULT; CONTRAST SENSITIVITY; DISCRIMINATION LEARNING; EYEGLASSES; FIXATION, OCULAR; HUMANS; NEURONAL PLASTICITY; ORIENTATION; PATTERN RECOGNITION, VISUAL; PERCEPTUAL MASKING; PHOTIC STIMULATION; TRANSFER (PSYCHOLOGY); VISUAL FIELDS; VISUAL PERCEPTION;

EID: 34047271080     PISSN: 00426989     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.visres.2006.10.028     Document Type: Article

References (52)

1. Abel P.L., O'Brien B.J., and Olavarria J.F. Organization of callosal linkages in visual area V2 of macaque monkey. Journal of Comparative Neurology 428 (2000) 278-293
2. Adini Y., Sagi D., and Tsodyks M. Excitatory-inhibitory network in the visual cortex: psychophysical evidence. Proceedings of the National Academy of Sciences United States of America 94 (1997) 10426-10431
3. Adini Y., Sagi D., and Tsodyks M. Context-enabled learning in the human visual system. Nature 415 (2002) 790-793
4. Andersen R.A. Multimodal integration for the representation of space in the posterior parietal cortex. Philosophical Transitions of Royal Society B: Biological Science 352 (1997) 1421-1428
5. Barlow H.B., and Reeves B.C. The versatility and absolute efficiency of detecting mirror symmetry in random dot patterns. Vision Research 19 (1979) 783-793
6. Bouma H. Interaction effects in peripheral letter recognition. Nature 226 (1970) 177-178
7. Clower D.M., Hoffman J.M., Votaw J.R., Faber T.L., Woods R.P., and Alexander G.E. Role of posterior parietal cortex in the recalibration of visually guided reaching. Nature 383 (1996) 618-621
8. Clarke S., and Miklossy J. Occipital cortex in man: Organization of callosal connections, related myelo- and cytoarchitecture, and putative boundaries of functional visual areas. Journal of Comparative Neurology 298 (1990) 188-214
9. Cunningham H.A., and Welch R.B. Multiple concurrent visual-motor mappings: implications for models of adaptation. Journal of Experimental Psychology: Human Perception and Performance 20 (1994) 987-999
10. Dakin S.C., and Watt R.J. Detection of bilateral symmetry using spatial filters. Spatial Vision 8 (1994) 393-413
11. Fiorentini A., and Berardi N. Perceptual learning specific for orientation and spatial frequency. Nature 287 (1980) 43-44
12. Freeman E., Sagi D., and Driver J. Lateral interactions between targets and flankers in low-level vision depend on attention to the flankers. Nature Neuroscience 4 (2001) 1032-1036
13. Gonshor A., and Melvill-Jones G. Extreme vertibulo-ocular adaptation induced by prolonged optical reversal of vision. Journal of Physiology 256 (1976) 381-414
14. Ghose G.M., Yang T., and Maunsell J.H. Physiological correlates of perceptual learning in monkey V1 and V2. Journal of Neurophysiology 87 (2002) 1867-1888
15. Giorgi R.G., Soong G.P., Woods R.L., and Peli E. Facilitation of contrast detection in near-peripheral vision. Vision Research 44 (2004) 3193-3202
16. Harris C.S. Perceptual adaptation to inverted, reversed, and displaced vision. Psychological Review 72 (1965) 419-444
17. Held R. Exposure-history as a factor in maintaining stability of perception and coordination. Journal of Nervous and Mental Disease 132 (1961) 26-32
18. Horton J.C., and Hoyt W.F. The representation of the visual field in human striate cortex. Archives of Ophthalmology 109 (1991) 816-824
19. Hochstein S., and Ahissar M. Hierarchies and reverse hierarchies in the visual system. Neuron 36 (2002) 791-804
20. Hubel D.H., and Wiesel T.N. Receptive fields and functional architecture of monkey striate cortex. Journal of Physiology 195 (1968) 215-243
21. Imamizu H., Miyauchi S., Tamada T., Sasaki Y., Takino R., Putz B., et al. Human cerebellar activity reflecting an acquired internal model of a new tool. Nature 403 (2000) 192-195
22. Kapadia M.K., Ito M., Gilvert C.D., and Westheimer G. Improvement in visual sensitivity by changes in local context: parallel studies in human observers and in V1 of alert monkeys. Neuron 15 (1995) 843-856
23. Karni A., and Sagi D. Where practice makes perfect. Proceedings of the National Academy of Sciences United States of America 88 (1991) 4966-4970
24. Kitazawa S., Kimura T., and Uka T. Prism adaptation of reaching movements: specificity for the velocity of reaching. Journal of Neuroscience 17 (1997) 1481-1492
25. Linden D.E., Kallenbach U., Heinecke A., Singer W., and Goebel R. The myth of upright vision A psychophysical and functional imaging study of adaptation to inverting spectacles. Perception 28 (1999) 469-481
26. Levi D.M., Hariharan S., and Klein S.A. Suppressive and facilitatory spatial interactions in peripheral vision: peripheral crowding is neither size independent nor simple contrast masking. Journal of Vision 2 (2002) 167-177
27. Misaki, M., Miyauchi, S., Tanaka, Y., Hashimoto, F., & Tashiro T. (2005). Retinotopic analysis of visual cortex reorganization after adaptation to reversing spectacles. 35th Annual meeting of Society for Neuroscience (abstract), Washington, DC, USA.
28. Miyauchi S., Egusa H., Amagase M., Sekiyama K., Imaruoka T., and Tashiro T. Adaptation to left-right reversed vision rapidly activates ipsilateral visual cortex in humans. Journal of Physiology (Paris) 98 (2004) 207-219
29. Pelli D.G., Palomares M., and Majaj N.J. Crowding is unlike ordinary masking: distinguishing feature integration from detection. Journal of Vision 4 (2004) 1136-1169
30. Polat U., Mizobe K., Pettet M.W., Kasamatsu T., and Norcia A.M. Collinear stimuli regulate visual responses depending on cell's contrast threshold. Nature 391 (1998) 580-584
31. Polat U., and Sagi D. Lateral interactions between spatial channels: suppression and facilitation revealed by lateral masking experiments. Vision Research 33 (1993) 993-999
32. Polat U., and Sagi D. Spatial interactions in human vision: from near to far via experience-dependent cascades of connections. Proceedings of the National Academy of Sciences United States of America 91 (1994) 1206-1209
33. Posner M.I., and Boies S.J. Components of attention. Psychological Review 78 (1971) 391-408
34. Redding G.M., and Wallace B. Adaptive eye-hand coordination: Implications of prism adaptation for perceptual-motor organization. In: Proteau L., and Elliott D. (Eds). Vision and motor control (1992), Holland, Amsterdam 105-128
35. Rollenhagen J.E., and Olson C.R. Mirror image confusion in single neurons of the macaque inferotemporal cortex. Science 287 (2000) 1506-1508
36. Rossetti Y., Rode G., Pisella L., Farne A., Li L., Boisson D., et al. Prism adaptation to a rightward optical deviation rehabilitates left hemispatial neglect. Nature 395 (1998) 166-169
37. Sekiyama K., Miyauchi S., Imaruoka H., Egusa H., and Tashiro T. Body image as a visuomotor transformation device revealed in adaptation to reversed vision. Nature 407 (2000) 374-377
38. Schoups A., Vogels R., Qian N., and Orban G.A. Practising orientation identification improves orientation coding in V1 neurons. Nature 412 (2001) 549-553
39. Shnai R., and Sagi D. Eccentricity effects on lateral interactions. Vision Research 45 (2005) 2009-2024
40. Shwartz S., Maquet P., and Frith C. Neural correlates of perceptual learning: a function MRI study of visual texture discrimination. Proceedings of the National Academy of Sciences United States of America 99 (2002) 17137-17142
41. Stratton G.M. Some preliminary experiments on vision without inversion of the retinal image. Psychological Review 3 (1896) 611-617
42. Sugita Y. Global plasticity in adult visual cortex following reversal of visual input. Nature 380 (1996) 523-526
43. Tanaka Y., and Sagi D. Perceptual memory for low contrast visual signals. Proceedings of the National Academy of Sciences United State of America 95 (1998) 12729-12733
44. Tanaka Y., and Sagi D. Attention and short-term memory in contrast detection. Vision Research 40 (2000) 1089-1100
45. Tanaka Y., and Sagi D. Fast learning of lateral interaction induced by temporal cueing. Investigative Ophthalmology and Visual Science 41 4 (2000) 49 ARVO abstract
46. Tanaka, Y., Miyauchi, S., & Misaki, M. Bilateral long-range interaction across right and left visual hemifield. Vision Research, in press.
47. Tyler C.W., Baseler H.A., Kontsevich L., Likova L.T., Wade A.R., and Wandall B.A. Predominantly extra-retinotopic cortical response to pattern symmetry. NeuroImage 24 (2005) 306-314
48. Van Essen D.C., and Mauncell J.H.R. Hierarchical organization and functional streams in the visual cortex. Trends in Neurosciences 6 (1983) 370-375
49. Von Helmholz, H. (1962). In J. P. C. Southall (Ed.), Helmholz's treatise on physiological optics, Vol. 3, Sect. 2. Translation from 3rd German Ed. pp. 242-270. New York, NY, Dover Press.
50. Welch R.B. Perceptual modification: Adapting to altered sensory environments (1978), Academic Press, New York
51. Williams C.B., and Hess R.F. Relationship between facilitation at threshold and suprathreshold contour integration. Journal of the Optical Society of America A Optics Image Science and Vision 15 (1998) 2046-2051
52. Zenger-Landolt B., and Koch C. Flanker effects in peripheral contrast discrimination-psychophysics and modelling. Vision Research 41 (2001) 3663-3675