Quantitative comparison between neural response in macaque inferotemporal cortex and behavioral discrimination of photographic images

Journal of Neurophysiology

Volumn 98, Issue 3, 2007, Pages 1263-1277

  Allred, Sarah R ^a   Jagadeesh, Bharathi ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ARTICLE; BEHAVIOR CHANGE; COMPARATIVE STUDY; MACACA; MALE; NERVE CELL; NONHUMAN; PHOTOGRAPHY; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; TASK PERFORMANCE; TEMPORAL CORTEX;

ANIMALS; DISCRIMINATION LEARNING; MACACA MULATTA; NEURONS; NEUROPHYSIOLOGY; PHOTOGRAPHY; PSYCHOPHYSIOLOGY; REACTION TIME; SACCADES; TEMPORAL LOBE; VISUAL PERCEPTION;

EID: 34548784389     PISSN: 00223077     EISSN: 15221598     Source Type: Journal    
DOI: 10.1152/jn.00016.2007     Document Type: Article

References (45)

1. Afraz SR, Kiani R, Esteky H. Microstimulation of inferotemporal cortex influences face categorization. Nature 442: 692-695, 2006.
2. Allred S, Liu Y, Jagadeesh B. Selectivity of inferior temporal neurons for realistic pictures predicted by algorithms for image database navigation. J Neurophysiol 94: 4068-4081, 2005.
3. Allred SR. The neural basis of visual object recognition. In: Neurobiology and Behavior. Seattle, WA: Univ. of Washington, 2006.
4. Bacon-Mace N, Mace MJ, Fabre-Thorpe M, Thorpe SJ. The time course of visual processing: backward masking and natural scene categorisation. Vision Res 45: 1459-1469, 2005.
5. Baylis GC, Driver J. Shape-coding in IT cells generalizes over contrast and mirror reversal, but not figure-ground reversal. Nat Neurosci 4: 937-942, 2001.
6. Brincat SL, Connor CE. Dynamic shape synthesis in posterior inferotemporal cortex. Neuron 49: 17-24, 2006.
7. Britten KH, Newsome WT, Shadlen MN, Celebrini S, Movshon JA. A relationship between behavioral choice and the visual responses of neurons in macaque MT. Vis Neurosci 13: 87-100, 1996.
8. Britten KH, Shadlen MN, Newsome WT, Movshon JA. The analysis of visual motion: a comparison of neuronal and psychophysical performance. J Neurosci 12: 4745-4765, 1992.
9. Cahusac PM, Miyashita Y, Rolls ET. Responses of hippocampal formation neurons in the monkey related to delayed spatial response and object-place memory tasks. Behav Brain Res 33: 229-240, 1989.
10. Chelazzi L, Duncan J, Miller EK, Desimone R. Responses of neurons in inferior temporal cortex during memory-guided visual search. J Neurophysiol 80: 2918-2940, 1998.
11. Enns JT, Di Lollo V. What's new in visual masking? Trends Cogn Sci 4: 345-352, 2000.
12. Enns JT, Di Lollo V. What competition? Trends Cogn Sci 6: 118, 2002.
13. Erickson CA, Jagadeesh B, Desimone R. Clustering of perirhinal neurons with similar properties following visual experience in adult monkeys. Nat Neurosci 3: 1143-1148, 2000.
14. Freedman DJ, Riesenhuber M, Poggio T, Miller EK. A comparison of primate prefrontal and inferior temporal cortices during visual categorization. J Neurosci 23: 5235-5246, 2003.
15. Fuchs AF, Robinson DA. A method for measuring horizontal and vertical eye movement chronically in the monkey. J Appl Physiol 21: 1068-1070, 1966.
16. Green DM, Swets JA. Signal Detection Theory and Psychophysics. New York: Wiley, 1966, p. 455.
17. Grill-Spector K, Kanwisher N. Visual recognition: as soon as you know it is there, you know what it is. Psychol Sci 16: 152-160, 2005.
18. Keysers C, Perrett DI. Visual masking and RSVP reveal neural competition. Trends Cogn Sci 6: 120-125, 2002.
19. Keysers C, Xiao DK, Foldiak P, Perrett DI. The speed of sight. J Cogn Neurosci 13: 90-101, 2001.
20. Kourtzi Z, DiCarlo JJ. Learning and neural plasticity in visual object recognition. Curr Opin Neurobiol 16: 152-158, 2006.
21. Kovacs G, Vogels R, Orban GA. Cortical correlate of pattern backward masking. Proc Natl Acad Sci USA 92: 5587-5591, 1995.
22. Leopold DA, Bondar IV, Giese MA. Norm-based face encoding by single neurons in the monkey inferotemporal cortex. Nature 442: 572-575, 2006.
23. Liu J, Newsome WT. Correlation between speed perception and neural activity in the middle temporal visual area. J Neurosci 25: 711-722, 2005.
24. Logothetis NK, Pauls J, Poggio T. Shape representation in the inferior temporal cortex of monkeys. Curr Biol 5: 552-563, 1995.
25. Matsumoto N, Okada M, Sugase-Miyamoto Y, Yamane S. Neuronal mechanisms encoding global-to-fine information in inferior-temporal cortex. J Comput Neurosci 18: 85-103, 2005.
26. Moran J, Desimone R. Selective attention gates visual processing in the extrastriate cortex. Science 229: 782-784, 1985.
27. Olson CR. Object-based vision and attention in primates. Curr Opin Neurobiol 11: 171-179, 2001.
28. Op de Beeck H, Wagemans J, Vogels R. Inferotemporal neurons represent low-dimensional configurations of parameterized shapes. Nat Neurosci 4: 1244-1252, 2001.
29. Rainer G, Lee H, Logothetis NK. The effect of learning on the function of monkey extrastriate visual cortex. PLoS Biol 2: E44, 2004.
30. Rieger JW, Braun C, Bulthoff HH, Gegenfurtner KR. The dynamics of visual pattern masking in natural scene processing: a magnetoencephalography study. J Vis 5: 275-286, 2005.
31. Rolls ET, Tovee MJ, Panzeri S. The neurophysiology of backward visual masking: information analysis. J Cogn Neurosci 11: 300-311, 1999.
32. Sereno AB, Maunsell JH. Shape selectivity in primate lateral intraparietal cortex. Nature 395: 500-503, 1998.
33. Shadlen MN, Britten KH, Newsome WT, Movshon JA. A computational analysis of the relationship between neuronal and behavioral responses to visual motion. J Neurosci 16: 1486-1510, 1996.
34. Sheinberg DL, Logothetis NK. The role of temporal cortical areas in perceptual organization. Proc Natl Acad Sci USA 94: 3408-3413, 1997.
35. Sheinberg DL, Logothetis NK. Noticing familiar objects in real world scenes: the role of temporal cortical neurons in natural vision. J Neurosci 21: 1340-1350, 2001.
36. Sheppard DM, Duncan J, Shapiro KL, Hillstrom AP. Objects and events in the attentional blink. Psychol Sci 13: 410-415, 2002.
37. Shih SI. Recall of two visual targets embedded in RSVP streams of distractors depends on their temporal and spatial relationship. Percept Psychophys 62: 1348-1355, 2000.
38. Sigala N, Logothetis NK. Visual categorization shapes feature selectivity in the primate temporal cortex. Nature 415: 318-320, 2002.
39. Sugase Y, Yamane S, Ueno S, Kawano K. Global and fine information coded by single neurons in the temporal visual cortex. Nature 400: 869-873, 1999.
40. Uka T, DeAngelis GC. Contribution of middle temporal area to coarse depth discrimination: comparison of neuronal and psychophysical sensitivity. J Neurosci 23: 3515-3530, 2003.
41. Uka T, Tanabe S, Watanabe M, Fujita I. Neural correlates of fine depth discrimination in monkey inferior temporal cortex. J Neurosci 25: 10796-10802, 2005.
42. Ungerleider L, Mishkin M. Two cortical visual systems. In: Analysis of Visual Behavior, edited by Ingle DJ, Goodale MA, Mansfield RJ. Cambridge, MA: MIT Press, 1982, p. 549-586.
43. VanRullen R, Thorpe SJ. Is it a bird? Is it a plane? Ultra-rapid visual categorisation of natural and artifactual objects. Perception 30: 655-668, 2001.
44. Vogels R, Biederman I, Bar M, Lorincz A. Inferior temporal neurons show greater sensitivity to nonaccidental than to metric shape differences. J Cogn Neurosci 13: 444-453, 2001.
45. Wichmann FA, Hill NJ. The psychometric function: I. Fitting, sampling, and goodness of fit. Percept Psychophys 63: 1293-1313, 2001.