Task-related modulation in the monkey inferotemporal cortex

Brain Research

Volumn 1121, Issue 1, 2006, Pages 76-82

  Sáry, Gyula ^a   Köteles, Károly ^a   Chadaide, Zoltán ^b   Tompa, Tamás ^a   Benedek, György ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

^b UNIVERSITY OF SZEGED   (Hungary)

Author keywords

Electrophysiology; Inferotemporal; Latency; Monkey; Task related; Vision

Indexed keywords

ANIMAL BEHAVIOR; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; INFORMATION PROCESSING; MONKEY; NONHUMAN; PRIORITY JOURNAL; RECOGNITION; TASK PERFORMANCE; TEMPORAL CORTEX;

ANIMALS; FIXATION, OCULAR; HAPLORHINI; NEURONS; PATTERN RECOGNITION, PHYSIOLOGICAL; REACTION TIME; REWARD; TEMPORAL LOBE;

ANIMALIA;

EID: 33750706570     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2006.08.106     Document Type: Article

References (34)

1. Azouz R., and Gray C.M. Cellular mechanisms contributing to response variability of cortical neurons in vivo. J. Neurosci. 19 (1999) 2209-2223
2. Baylis G.C., Rolls E.T., and Leonard C.M. Functional subdivisions of the temporal lobe neocortex. J. Neurosci. 7 (1987) 330-342
3. Commenges D., and Seal J. The analysis of neuronal discharge sequences: change-point estimation and comparison of variances. Stat. Med. 4 (1985) 91-104
4. Dean P. Effects of inferotemporal lesions on the behavior of monkeys. Psychol. Bull. 83 (1976) 41-71
5. Desimone R., and Ungerleider L.G. Multiple visual areas in the caudal superior temporal sulcus of the macaque. J. Comp. Neurol. 248 (1986) 164-189
6. Desimone R., Albright T.D., Gross C.G., and Bruce C. Stimulus-selective properties of inferior temporal neurons in the macaque. J. Neurosci. 4 (1984) 2051-2062
7. Edwards R., Xiao D., Keysers C., Foldiak P., and Perrett D. Color sensitivity of cells responsive to complex stimuli in the temporal cortex. J. Neurophysiol. 90 (2003) 1245-1256
8. Friedman H.S., and Priebe C.E. Smoothing bandwidth selection for response latency estimation. J. Neurosci. Methods 87 (1999) 13-16
9. Fuster J.M., and Jervey J.P. Inferotemporal neurons distinguish and retain behaviorally relevant features of visual stimuli. Science 212 (1981) 952-955
10. Hanes D.P., Thompson K.G., and Schall J.D. Relationship of presaccadic activity in frontal eye field and supplementary eye field to saccade initiation in macaque: Poisson spike train analysis. Exp. Brain Res. 103 (1995) 85-96
11. Judge S.J., Richmond B.J., and Chu F.C. Implantation of magnetic search coils for measurement of eye position: an improved method. Vision Res. 20 (1980) 535-538
12. Kiani R., Esteky H., and Tanaka K. Differences in onset latency of macaque inferotemporal neural responses to primate and non-primate faces. J. Neurophysiol. 94 (2005) 1587-1596
13. Kovacs G., Sary G., Koteles K., Chadaide Z., Tompa T., Vogels R., and Benedek G. Effects of surface cues on macaque inferior temporal cortical responses. Cereb. Cortex 13 (2003) 178-188
14. Liu Z., and Richmond B.J. Response differences in monkey TE and perirhinal cortex: stimulus association related to reward schedules. J. Neurophysiol. 83 (2000) 1677-1692
15. Logothetis N.K., and Sheinberg D.L. Visual object recognition. Annu. Rev. Neurosci. 19 (1996) 577-621
16. Martinez-Trujillo J.C., and Treue S. Feature-based attention increases the selectivity of population responses in primate visual cortex. Curr. Biol. 14 (2004) 744-751
17. Moran J., and Desimone R. Selective attention gates visual processing in the extrastriate cortex. Science 229 (1985) 782-784
18. Reynolds J.H., and Chelazzi L. Attentional modulation of visual processing. Annu. Rev. Neurosci. 27 (2004) 611-647
19. Richmond B.J., and Sato T. Enhancement of inferior temporal neurons during visual discrimination. J. Neurophysiol. 58 (1987) 1292-1306
20. Roelfsema P.R., Lamme V.A., and Spekreijse H. Object-based attention in the primary visual cortex of the macaque monkey. Nature 395 (1998) 376-381
21. Rolls E.T., and Tovee M.J. Sparseness of the neuronal representation of stimuli in the primate temporal visual cortex. J. Neurophysiol. 73 (1995) 713-726
22. Rolls E.T., Cahusac P.M., Feigenbaum J.D., and Miyashita Y. Responses of single neurons in the hippocampus of the macaque related to recognition memory. Exp. Brain Res. 93 (1993) 299-306
23. Sary G., Chadaide Z., Tompa T., Kovacs G., Koteles K., Boda K., Raduly L., and Benedek G. Relationship between stimulus complexity and neuronal activity in the inferotemporal cortex of the macaque monkey. Brain Res. Cogn. Brain Res. 22 (2004) 1-12
24. Sato T. Effects of attention and stimulus interaction on visual responses of inferior temporal neurons in macaque. J. Neurophysiol. 60 (1988) 344-364
25. Tamura H., and Tanaka K. Visual response properties of cells in the ventral and dorsal parts of the macaque inferotemporal cortex. Cereb. Cortex 11 (2001) 384-399
26. Tanaka K. Inferotemporal cortex and object vision. Annu. Rev. Neurosci. 19 (1996) 109-139
27. Tanaka H., Onoe H., Tsukada H., and Fujita I. Attentional modulation of neural activity in the macaque inferior temporal cortex during global and local processing. Neurosci. Res. 39 (2001) 469-472
28. Tanaka H., Uka T., Yoshiyama K., Kato M., and Fujita I. Processing of shape defined by disparity in monkey inferior temporal cortex. J. Neurophysiol. 85 (2001) 735-744
29. Thompson K.G., Hanes D.P., Bichot N.P., and Schall J.D. Perceptual and motor processing stages identified in the activity of macaque frontal eye field neurons during visual search. J. Neurophysiol. 76 (1996) 4040-4055
30. Tompa T., Sary G., Chadaide Z., Koteles K., Kovacs G., and Benedek G. Achromatic shape processing in the inferotemporal cortex of the macaque. NeuroReport 16 (2005) 57-61
31. Ungerleider L.G., and Mishkin M. Two cortical visual systems. In: Ingle D.J., Goodale M.A., and Mansfield R.J.W. (Eds). Analysis of Visual Behaviour (1982), The MIT Press 549-585
32. Vogels R., Sary G., and Orban G.A. How task-related are the responses of inferior temporal neurons?. Vis. Neurosci. 12 (1995) 207-214
33. Wang Y., Fujita I., and Murayama Y. Neuronal mechanisms of selectivity for object features revealed by blocking inhibition in inferotemporal cortex. Nat. Neurosci. 3 (2000) 807-813
34. Womelsdorf T., Fries P., Mitra P.P., and Desimone R. Gamma-band synchronization in visual cortex predicts speed of change detection. Nature 439 (2006) 733-736