A reexamination of the concurrent discrimination learning task: The importance of the anteror inferotemporal cortex, area TE

Behavioral Neuroscience

Volumn 112, Issue 1, 1998, Pages 3-14

  Buffalo, Elizabeth A ^c   Stefanacci, Lisa ^c   Squire, Larry R ^a   Zola, Stuart M ^a,b  

^a VA SAN DIEGO HEALTHCARE SYSTEM   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN INJURY; CONTROLLED STUDY; DISCRIMINATION LEARNING; FEMALE; HISTOPATHOLOGY; MALE; MONKEY; NONHUMAN; PATHOPHYSIOLOGY; TASK PERFORMANCE; TEMPORAL CORTEX; TEMPORAL LOBE;

ANIMALS; ASSOCIATION LEARNING; ATTENTION; BRAIN MAPPING; COLOR PERCEPTION; CONDITIONING, OPERANT; DEPTH PERCEPTION; DISCRIMINATION LEARNING; FEMALE; MACACA FASCICULARIS; MALE; PATTERN RECOGNITION, VISUAL; PSYCHOMOTOR PERFORMANCE; RETENTION (PSYCHOLOGY); TEMPORAL LOBE;

EID: 0031908554     PISSN: 07357044     EISSN: None     Source Type: Journal    
DOI: 10.1037/0735-7044.112.1.3     Document Type: Article

References (47)

1. Alvarez, P. Zola-Morgan, S., & Squire, L. R. (1995). Damage limited to the hippocampal region produces long-lasting memory impairinent in monkeys. Journal of Neuroscience, 15, 3796-3807.
2. Amaral, D. G., Insausti, R., & Cowan, W. M. (1987). The entorhinal cortex of the monkey: I. Cytoarchitectonie organization. Journal of Comparative Neurology, 264, 326-355.
3. Baizer, J. S., Ungerleider, L. G., & Desimone, R. (1991). Organization of visual inputs to the inferior temporal and posterior parietal cortex in macaques. Journal of Neuroscience, 11, 168-190.
4. Bonin, G. V., & Bailey, P. (1947). The neocortex of Macaca mulatta. Urbana: University of Illinois Press.
5. Buckley, M. J., & Gaffan, D. (1997). Impairment of visual object-discrimination learning after perirhinal cortex ablation. Behavioral Neuroscience. 111, 467-475.
6. Buffalo, E. A., Ramus, S. J., Zola-Morgan, S., & Squire, L. R. (1995). Different behavioral effects of damage to visual area TE and perirhinal cortex. Society for Neuroscience Abstracts. 21, 1493.
7. Buffalo, E. A., Zola-Morgan, S., & Squire, L. R. (1994). Inferotemporal cortex area TE as redefined by recent anatomical studies. Society for Neuroscience Abstracts, 20, 1074.
8. Correll, R. E., & Scoville, W. B. (1965), Effects of medial temporal lesions on visual discrimination performance. Journal of Comparative Physiology and Psychology, 60, 175-181.
9. Correll, R. E., & Scoville, W. B. (1970). Relationship of ITI to acquisition of .serial visual discrimination following temporal rhinencephalic resection in monkeys. Journal of Comparative Physiology and Psychology, 70, 464-469.
10. Gaffan, D., & Murray, E. A. (1992). Monkeys (Macaca fascicularis) with rhinal cortex ablations succeed in object discrimination learning despite 24-hour intertrial intervals and fail at matching to sample despite double sample presentations. Behavioral Neuroscience, 106, 30-38.
11. Gattas, R., Sousa, A. P. B., & Covery, E. (1985). Cortical visual areas of the macaque: Possible substrates for pattern recognition mechanisms. In C. Chagas, R. Gattas, & C. Gross (Eds.), Pattern recognition mechanisms (pp. 1-20). Vatican City: Pontifica Academia Scientiarum.
12. Gellerman, L. W. (1933). Chance orders of alternating stimuli in visual discrimination experiments. Journal of Genetics Psychology. 42, 207-208.
13. Gross, C. G., Rocha-Miranda, C. E., & Bender, D. B. (1972). Visual properties of neurons in inferotemporal cortex of the macaque. Journal of Neurophysiology, 35, 96-111.
14. Harlow, H., & Bromer, J. A. (1938). A test-apparatus for monkeys. Psychological Review, 19, 434-438.
15. Insausti, R., Amaral, D. G., & Cowan, W. M. (1987). The entorhinal of the monkey: II. Cortical afferents. Journal of Comparative Neurologv, 264, 356-395.
16. Iwai, E., & Mishkin, M. (1968). Two visual foci in the temporal lobe of monkeys. In N. Yoshii & N. A. Buchwald (Eds.), Neurophysiological basis of learning and behavior (pp. 1-11). Japan: Osaka University Press.
17. Knowlton, B. J., Mangels, J. A., & Squire, L. R. (1996). A neostriatal habit learning system in humans. Science, 273, 1399-1402.
18. Mahut, H., Zola-Morgan, S., & Moss, M. (1982). Hippocampal resections impair associative learning recognition memory in the monkey. Journal of Neuroscience, 2, 1214-1229.
19. Malamut, B., Saunders, R., & Mishkin, M. (1984). Monkeys with combined amygdalo-hippocampal lesions succeed in object discrimination learning despite 24-hour intertriai intervals. Behavioral Neuroscience, 98, 759-769.
20. Malkova, L., Mishkin, M., & Bachevalier. J. (1995). Long-term effects of selective neonatal temporal lobe lesions on learning and memory in monkeys. Behavioral Neuroscience, 109, 212-226.
21. Meunier, M., Bachevalier, J., Mishkin, M., & Murray, E. A. (1993). Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys. Journal of Neuroscience, 13, 5418-5432.
22. Mishkin, M. (1982). A memory system in the monkey. Philosophical Transactions of the Royal Society (London), 298, 85-92.
23. Mishkin, M., & Murray, E. A. (1994). Stimulus recognition. Current Opinion in Neurobiology, 4, 200-206.
24. Moss, M., Mahut, H., & Zola-Morgan, S. (1981). Concurrent discrimination learning of monkeys after hippocampal. entorhinal. or fornix lesions. Journal of Neuroscience. 1, 227-240.
25. Murray, E. A. (1996). What have ablation studies told us about the neural substates of stimulus memory? Seminars in the Neurosciences. 8, 13-22.
26. Orbach, J., Milner, B., & Rasmussen, T. (1960). Learning and retention in monkeys after amygdala-hippocampus resection. Archives of Neurology, 3, 230-251.
27. Oscar-Berman, M., & Zola-Morgan, S. M. (1980). Comparative neuropsychology and Korsakoff's syndrome. II.-Two-choice visual discrimination learning. Neuropsychologia, 18, 513-525.
28. Phillips, R. R., Malamut, B. L., Bachevalier, J., & Mishkin, M. (1988). Dissociation of the effects of inferior temporal and limbic lesions on object discrimination learning with 24-hour intertrial intervals. Behavioural Brain Research, 27, 99-107.
29. Scoville, W. B., & Milner, B. (1957). Loss of recent memory after bilateral hippocampal lesions. Journal of Neurology, Neurosurgery and Psychiatry, 20, 11-21.
30. Squire, L. R., & Zola-Morgan, S. (1983). The neurology of memory: The case for correspondence between the findings for human and nonhumun primate. In J. A. Deutsch (Ed.), The physiological basis of memory (pp. 199-268). New York: Academic Press.
31. Squire, L. R., & Zola-Morgan, S. (1991). The medial temporal lobe memory system. Science, 253, 1380-1386.
32. Squire, L. R., Zola-Morgan, S., & Chen, K. S. (1988). Human amnesia and animal models of amnesia: Performance of amnesic patients on tests designed for the monkey. Behavioral Neuroscience, 102, 210-221.
33. Suzuki, W. A., (1996). The anatomy, physiology and functions of the perirhinal cortex. Current Opinion in Neurobiology, 6, 179-186.
34. Suzuki, W. A., & Amaral, D. G. (1994a). The perirhinal and parahippocampal cortices of the macaque monkey: Conical afferents. Journal of Comparative Neurology, 350, 497-533.
35. Suzuki, W. A., & Amaral, D. G. (1994b). Topographic organization of the reciprocal connections between the monkey entorhinal cortex and the perirhinal and parahippocampal cortices. Journal of Neuroscience, 14, 1856-1877.
36. Suzuki, W. A., Zola-Morgan, S., Squire, L. R., & Amaral, D. G. (1993). Lesions of the perirhinal and parahippocampal cortices in the monkey produce long-lasting memory impairment in the visual and tactual modalities. Journal of Neuroscience. 13, 2430-2451.
37. Tanaka, K. (1996). Inferotemporal cortex and object vision. Annual Review of Neuroscience. 19, 109-139.
38. Thornton, J. A., Rothblat, L. A., & Murray, E. A. (1997). Rhinal cortex removal produces amnesia tor preoperatively learned discrimination problems but fails to disrupt postoperative acquisition and retention in rhesus monkeys. Journal of Neuroscience. 17, 8536-8549.
39. Zola-Morgan, S., & Squire, L. R. (1984,). Preserved learning in monkeys with medial temporal lesions: Sparing of motor and cognitive skills. Journal of Neuroscience, 4, 1072-1085.
40. Zola-Morgan, S., & Squire, L. R. (1985). Medial temporal lesions in monkeys impair memory on a variety of tasks sensitive to human amnesia. Behavioral Neuroscience, 99, 22-34.
41. Zola-Morgan, S., Squire, L. R., & Amaral, D. G. (1989a). Lesions of the amygdala that spare adjacent cortical regions do not impair memory or exacerbate the impairment following lesions of the hippocampal formation. Journal of Neuroscience, 9, 1922-1936.
42. Zola-Morgan, S., Squire, L. R., & Amaral, D. G. (1989b). Lesions of the hippocampal formation but not lesions of the fornix or the mammillary nuclei produce long-lasting memory impairment in monkeys. Journal of Neuroscience, 9, 898-913.
43. Zola-Morgan, S., Squire, L. R., Amaral, D. G., & Suzuki, W. A. (1989). Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment. Journal of Neuroscience, 9, 4355-4370.
44. Zola-Morgan, S., Squire, L. R., Glower, R. P., & Rempel, N. L. (1993). Damage to the perirhinal cortex exacerbates memory impairment following lesions to the hippocampal formation. Journal of Neuroscience, 13, 251-265.
45. Zola-Morgan, S., Squire, L. R., & Mishkin, M. (1982). The neuroanatomy of amnesia: Amygdala-hippocampus versus temporal stem. Science, 218, 1337-1339.
46. Zola-Morgan, S., Squire, L. R., Ramus, S. J. (1994). Severity of memory impairment in monkeys as a function of locus and extent of damage within the medial temporal lobe memory system. Hippocampus, 4, 83-495.
47. Zola-Morgan, S., Squire, L. R., Rempel, N. L., Clower, R. P., & Amaral, D. G. (1992). Enduring memory impairment in monkeys after ischemic damage to the hippocampus. Journal of Neuroscience, 12, 2582-2596.