Using computational modelling to understand cognition in the ventral visual-perirhinal pathway

Computational Neuroscience for Advancing Artificial Intelligence: Models, Methods and Applications

Volumn , Issue , 2010, Pages 15-45

  Cowell, Rosemary A ^a   Bussey, Timothy J ^b   Saksida, Lisa M ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84866327187     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.4018/978-1-60960-021-1.ch002     Document Type: Chapter

References (103)

1. Baker, C. I., Behrmann, M., & Olson, C. R. (2002). Impact of learning on representation of parts and wholes in monkey inferotemporal cortex. Nature Neuroscience, 5, 1210-1216.doi:10.1038/nn960
2. Barense, M. D., Bussey, T. J., Lee, A. C., Rogers, T. T., Davies, R. R., & Saksida, L. M. (2005). Functional specialization in the human medial temporal lobe. The Journal of Neuroscience, 25(44), 10239-10246.doi:10.1523/JNEUROSCI.2704-05.2005
3. Barense, M. D., Bussey, T. J., Lee, A. C. H., Rogers, T. T., Davies, R. R., & Saksida, L. M. (2005). Functional specialization in the human medial temporal lobe. The Journal of Neuroscience, 25, 10239-10246.doi:10.1523/JNEUROSCI.2704-05.2005
4. Barense, M. D., Gaffan, D., & Graham, K. S. (2007). The human medial temporal lobe processes online representations of complex objects. Neuropsychologia, 45(13), 2963-2974.doi:10.1016/j.neuropsychologia.2007.05.023
5. Bartko, S. J., Winters, B. D., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2007a). Perceptual functions of perirhinal cortex in rats: zero-delay object recognition and simultaneous oddity discriminations. The Journal of Neuroscience, 27(10), 2548-2559.doi:10.1523/JNEUROSCI.5171-06.2007
6. Bartko, S. J., Winters, B. D., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2007b). Perirhinal cortex resolves feature ambiguity in configural object recognition and perceptual oddity tasks. Learning & Memory (Cold Spring Harbor, N.Y.), 14(12), 821-832.doi:10.1101/lm.749207
7. Baxter, M. G. (2009). Involvement of medial temporal lobe structures in memory and perception. Neuron, 61(5), 667-677.doi:10.1016/j. neuron.2009.02.007
8. Blake, L., Jarvis, C. D., & Mishkin, M. (1977). Pattern discrimination thresholds after partial inferior temporal of lateral striate lesions in monkeys. Brain Research, 120, 209-220.doi:10.1016/00068993(77)90901-5
9. Buckley, M. J. (2005). The role of the medial temporal lobe in memory and perception: evidence from rats, nonhuman primates and humans. Quarterly Journal of Experimental Psychology, 58B, 246-268.
10. Buckley, M. J., & Gaffan, D. (1997). Impairment of visual object-discrimination learning after perirhinal cortex ablation. Behavioral Neuroscience, 111, 467-475.doi:10.1037/0735-7044.111.3.467
11. Buckley, M. J., & Gaffan, D. (1998a). Perirhinal cortex ablation impairs configural learning and paired-associate learning equally. Neuropsychologia, 36, 535-546.doi:10.1016/S00283932(97)00120-6
12. Buckley, M. J., & Gaffan, D. (1998b). Perirhinal cortex ablation impairs visual object identification. The Journal of Neuroscience, 18, 2268-2275.
13. Buffalo, E. A., Ramus, S. J., Clark, R. E., Teng, E., Squire, L. R., & Zola, S. M. (1999). Dissociation between the effects of damage to perirhinal cortex and area TE. Learning & Memory (Cold Spring Harbor, N.Y.), 6, 572-599.doi:10.1101/lm.6.6.572
14. Buffalo, E. A., Ramus, S. J., Squire, L. R., & Zola, S. M. (2000). Perception and recognition memory in monkeys following lesions of area TE and perirhinal cortex. Learning & Memory (Cold Spring Harbor, N.Y.), 7(6), 375-382.doi:10.1101/ lm.32100
15. Buffalo, E. A., Reber, P. J., & Squire, L. R. (1998). The human perirhinal cortex and recognition memory. Hippocampus, 8, 330-339.doi:10.1002/SICI)1098-1063(1998)8:4<330::AIDHIPO3>3.0.CO;2-L
16. Bussey, T. J. (2004). Multiple memory systems: Fact or fiction? Quarterly Journal of Experimental Psychology, 57, 89-94.
17. Bussey, T. J., & Saksida, L. M. (2002). The organization of visual object representations: a connectionist model of effects of lesions in perirhinal cortex. The European Journal of Neuroscience, 15(2), 355-364.doi:10.1046/j.0953816x.2001.01850.x
18. Bussey, T. J., & Saksida, L. M. (2002). The organization of visual object representations: A connectionist model of effects of lesions in perirhinal cortex. The European Journal of Neuroscience, 15, 355-364.doi:10.1046/j.0953-816x.2001.01850.x
19. Bussey, T. J., & Saksida, L. M. (2005). Object memory and perception in the medial temporal lobe: An alternative approach. Current Opinion in Neurobiology, 15, 730-737.doi:10.1016/j.conb.2005.10.014
20. Bussey, T. J., & Saksida, L. M. (2007). Memory, perception, and the ventral visual-perirhinalhippocampal stream: thinking outside of the boxes. Hippocampus, 17(9), 898-908.doi:10.1002/ hipo.20320
21. Bussey, T. J., Saksida, L. M., & Murray, E. A. (2002). Perirhinal cortex resolves feature ambiguity in complex visual discriminations. The European Journal of Neuroscience, 15, 365-374. doi:10.1046/j.0953-816x.2001.01851.x
22. Bussey, T. J., Saksida, L. M., & Murray, E. A. (2003). Impairments in visual discrimination after perirhinal cortex lesions: Testing 'declarative' versus 'perceptual-mnemonic' views of perirhinal cortex function. The European Journal of Neuroscience, 17, 649-660.doi:10.1046/j.14609568.2003.02475.x
23. Bussey, T. J., Saksida, L. M., & Murray, E. A. (2005). The PMFC model of perirhinal cortex function. Quarterly Journal of Experimental Psychology, 58B, 269-282.
24. Butter, C. M. (1972). Detection of Masked Patterns in Monkeys with Inferotemporal, Striate or Dorsolateral Frontal Lesions. Neuropsychologia, 10, 241-243.doi:10.1016/0028-3932(72)90066-8
25. Churchland, P. S., & Sejnowski, T. J. (1988). Perspectives on Cognitive Neuroscience. Science, 242(4879), 741-745.doi:10.1126/science.3055294
26. Churchland, P. S., & Sejnowski, T. J. (1992). The Computational Brain. Cambridge: MIT Press.
27. Cowell, R. A. (2006). Modelling the effects of damage to perirhinal cortex and ventral visual stream on visual cognition. Unpublished dissertation, University of Oxford, UK.
28. Cowell, R. A., Bussey, T. J., & Saksida, L. M. (2006). Why does brain damage impair memory? A connectionist model of object recognition memory in perirhinal cortex. The Journal of Neuroscience, 26(47), 12186-12197.doi:10.1523/JNEUROSCI.2818-06.2006
29. Cowell, R. A., Bussey, T. J., & Saksida, L. M. (2010). Functional dissociations within the ventral object processing pathway: cognitive modules or a hierarchical continuum? Journal of Cognitive Neuroscience, 22(11), 2460-2479.doi:10.1162/jocn.2009.21373
30. Cowey, A., & Gross, C. G. (1970). Effects of foveal prestriate and inferotemporal lesions on visual discrimination by rhesus monkeys. Experimental Brain Research, 11(2), 128-144.doi:10.1007/BF00234318
31. Dean, P. (1974). Choice reaction times for pattern discriminations in monkeys with inferotemporal lesions. Neuropsychologia, 12, 465-476. doi:10.1016/0028-3932(74)90076-1
32. Devlin, J. T., & C.J., P. (2007). Perirhinal contributions to human visual perception. Current Biology, 17(17), 1484-1488.doi:10.1016/j.cub.2007.07.066
33. Dickinson, A. (1980). Contemporary animal learning theory (1st ed.). Cambridge: Cambridge University Press.
34. Eacott, M. J., Gaffan, D., & Murray, E. A. (1994). Preserved recognition memory for small sets, and impaired stimulus identification for large sets, following rhinal cortex ablations in monkeys. The European Journal of Neuroscience, 6, 1466-1478. doi:10.1111/j.1460-9568.1994.tb01008.x
35. Eacott, M. J., & Gaffan, E. A. (2005). The roles of the perirhinal cortex, postrhinal cortex, and the fornix in memory for objects, contexts, and events in the rat. Qaurterly Journal of Experimental Psychology, 58B, 202-217. doi:10.1080/02724990444000203
36. Forwood, S. E., Winters, B. D., & Bussey, T. J. (2005). Hippocampal lesions that abolish spatial maze performance spare object recognition memory at delays of up to 48 hours. Hippocampus, 15, 347-355.doi:10.1002/hipo.20059
37. Fuster, J. (2003). Cortex and Mind. Oxford: Oxford university Press.
38. Gaffan, D. (2002). Against memory systems. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 357, 1111-1121.doi:10.1098/rstb.2002.1110
39. Gaffan, D., & Murray, E. A. (1992). Monkeys (Macaca fascicularis) with rhinal cortex ablations succeed in object discrimination learning despite 24-hr intertrial intervals and fail at matching to sample despite double sample presentations. Behavioral Neuroscience, 106, 30-38. doi:10.1037/0735-7044.106.1.30
40. Gilbert, P. E., & Kesner, R. P. (2003). Recognition memory for complex visual discriminations is influenced by stimulus interference in rodents with perirhinal cortex damage. Learning & Memory (Cold Spring Harbor, N.Y.), 10(6), 525-530. doi:10.1101/lm.64503
41. Goulet, S., & Murray, E. A. (2001). Neural substrates of crossmodal association memory in monkeys: the amygdala versus the anterior rhinal cortex. Behavioral Neuroscience, 115(2), 271-284.doi:10.1037/0735-7044.115.2.271
42. Gross, C. G., Cowey, A., & Manning, F. J. (1971). Further analysis of visual discrimination deficits following foveal prestriate and inferotemporal lesions in rhesus monkeys. Journal of Comparative and Physiological Psychology, 76(1), 1-7. doi:10.1037/h0031039
43. Hampton, R. R. (2005). Monkey perirhinal cortex is critical for visual memory, but not for visual perception: Re-examination of the behavioural evidence from monkeys. Quarterly Journal of Experimental Psychology, 58B, 283-299.
44. Hartley, T., Bird, C. M., Chan, D., Cipolotti, L., Husain, M., & Vargha-Khadem, F. (2007). The hippocampus is required for short-term topographical memory in humans. Hippocampus, 17(1), 34-48. doi:10.1002/hipo.20240
45. Holdstock, J. S., Shaw, C., & Aggleton, J. P. (1995). The performance of amnesic subjects on tests of delayed matching-to-sample and delayed matching-to-position. Neuropsychologia, 33(12), 1583-1596.doi:10.1016/0028-3932(95)00145-X
46. Iversen, S. D., & Humphrey, N. K. (1971). Ventral temporal lobe lesions and visual oddity performance. Brain Research, 30(2), 253-263. doi:10.1016/0006-8993(71)90077-1
47. Iwai, E., & Mishkin, M. (1968). Two visual foci in the temporal lobe of monkeys. In Yoshii, N., & Buchwald, N. (Eds.), Neurophysiological basis of learning and behavior (pp. 1-11). Japan: Osaka University Press.
48. Kikuchi, R., & Iwai, E. (1980). The locus of the posterior subdivision of the inferotemporal visual learning area in the monkey. Brain Research, 198(2), 347-360.doi:10.1016/00068993(80)90749-0
49. Lee, A. C., Bandelow, S., Schwarzbauer, C., Henson, R. N., & Graham, K. S. (2006). Perirhinal cortex activity during visual object discrimination: an event-related fMRI study. NeuroImage, 33(1), 362-373.doi:10.1016/j.neuroimage.2006.06.021
50. Lee, A. C., Buckley, M. J., Gaffan, D., Emery, T., Hodges, J. R., & Graham, K. S. (2006). Differentiating the roles of the hippocampus and perirhinal cortex in processes beyond long-term declarative memory: a double dissociation in dementia. The Journal of Neuroscience, 26(19), 5198-5203. doi:10.1523/JNEUROSCI.3157-05.2006
51. Lee, A. C., Buckley, M. J., Pegman, S. J., Spiers, H., Scahill, V. L., & Gaffan, D. (2005). Specialization in the medial temporal lobe for processing of objects and scenes. Hippocampus, 15(6), 782-797. doi:10.1002/hipo.20101
52. Lee, A. C., Levi, N., Davies, R. R., Hodges, J. R., & Graham, K. S. (2007). Differing profiles of face and scene discrimination deficits in semantic dementia and Alzheimer's disease. Neuropsychologia, 45(9), 2135-2146.doi:10.1016/j.neuropsychologia.2007.01.010
53. Lee, A. C., Scahill, V. L., & Graham, K. S. (2008). Activating the medial temporal lobe during oddity judgment for faces and scenes. Cerebral Cortex, 18(3), 683-696.doi:10.1093/cercor/bhm104
54. Levy, D. A., Shrager, Y., & Squire, L. R. (2005). Intact visual discrimination of complex and feature-ambiguous stimuli in the absence of perirhinal cortex. Learning & Memory (Cold Spring Harbor, N.Y.), 12(1), 61-66.doi:10.1101/lm.84405
55. Mackintosh, N. J. (1974). The psychology of animal learning. London: Academic Press.
56. Manning, F. J. (1971a). Punishment for errors and visual-discrimination learning by monkeys with inferotemporal cortex lesions. Journal of Comparative and Physiological Psychology, 75(1), 146-152.doi:10.1037/h0030675
57. Manning, F. J. (1971b). The selective attention "deficit" of monkeys with ablations of foveal prestriate cortex. Psychonomic Science, 25(5), 291-292.
58. Manns, J. R., Stark, C. E., & Squire, L. R. (2000). The visual paired-comparison task as a measure of declarative memory. Proceedings of the National Academy of Sciences of the United States of America, 97(22), 12375-12379.doi:10.1073/ pnas.220398097
59. Marr, D., & Poggio, T. (1977). From understanding computation to understanding neural circuitry. Neurosciences Research Program Bulletin, 15, 470-488.
60. McClelland, J. L., & Rumelhart, D. E. (Eds.). (1986). Parallel Distributed Processing: Explorations in the Microstructure of Cognition (Vol. 2). Cambridge, MA: MIT Press.
61. 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. The Journal of Neuroscience, 13, 5418-5432.
62. Mishkin, M. (1982). A memory system in the monkey. [Biology]. Philosophical Transactions of the Royal Society of London, 298, 83-95. doi:10.1098/rstb.1982.0074
63. Moss, H. E., Rodd, J. M., Stamatakis, E. A., Bright, P., & Tyler, L. K. (2005). Anteromedial temporal cortex supports fine-grained differentiation among objects. Cereb Cortex, 15(5), 616-627. doi:10.1093/cercor/bhh163
64. Mumby, D. G., & Pinel, J. P. (1994). Rhinal cortex lesions and object recognition in rats. Behavioral Neuroscience, 108(1), 11-18.doi:10.1037/07357044.108.1.11
65. Murray, E. A. (2000). Memory for objects in nonhuman primates. In Gazzaniga, M. S. (Ed.), The new cognitive neurosciences. London: The MIT Press.
66. Murray, E. A., & Bussey, T. J. (1999). Perceptualmnemonic functions of perirhinal cortex. Trends in Cognitive Sciences, 3, 142-151.doi:10.1016/S1364-6613(99)01303-0
67. Murray, E. A., Málková, L., & Goulet, S. (1998). Crossmodal associations, intramodal associations, and object identification in macaque monkeys. In Milner, A. D. (Ed.), Comparative Neuropsychology (pp. 51-69). Oxford: Oxford University Press.
68. Norman, G., & Eacott, M. J. (2004). Impaired object recognition with increasing levels of feature ambiguity in rats with perirhinal cortex lesions. Behavioural Brain Research, 148(1-2), 79-91. doi:10.1016/S0166-4328(03)00176-1
69. Norman, K. A., & O'Reilly, R. C. (2003). Modeling hippocampal and neocortical contributions to recognition memory: a complementary-learning-systems approach. Psychological Review, 110(4), 611-646.doi:10.1037/0033-295X.110.4.611
70. O'Reilly, R. C. (1998). Six Principles for Biological Based Computational Models of Cortical Cognition. Trends in Cognitive Sciences, 2(11), 455-462.doi:10.1016/S1364-6613(98)01241-8
71. Osterrieth, P. (1944). Filetest de copie d'une figure complex: Contribution a l'etude de la perception et de la memoire [The test of copying a complex figure: A contribution to the study of perception and memory]. Archives de Psychologie, 30, 286-356.
72. Palmeri, T. J., & Gauthier, I. (2004). Visual Object Understanding. Nature Reviews. Neuroscience, 5, 291-304.doi:10.1038/nrn1364
73. Plaut, D. C. (1995). Double dissociation without modularity: evidence from connectionist neuropsychology. Journal of Clinical and Experimental Neuropsychology, 17, 291-321. doi:10.1080/01688639508405124
74. Popper, K. (1999). All Life is Problem Solving. London: Routledge.
75. Preston, A. R., & Gabrieli, J. D. (2008). Dissociation between explicit memory and configural memory in the human medial temporal lobe. Cerebral Cortex, 18(9), 2192-2207.doi:10.1093/cercor/bhm245
76. Rolls, E. T., & Deco, G. (2002). Computational Neuroscience of Vision. New York: Oxford University Press Inc.
77. Rosenthal, O., & Behrmann, M. (2006). Acquiring long-term representations of visual classes following extensive extrastriate damage. Neuropsychologia, 44(5), 799-815. doi:10.1016/j.neuropsychologia.2005.07.010
78. Rumelhart, D. E., & McClelland, J. L. (Eds.). (1986). Parallel Distributed Processing: Explorations in the Microstructure of Cognition (Vol. 1). Cambridge, MA: MIT Press.
79. Sakai, S., & Miyashita, Y. (1993). Memory and imagery in the temporal lobe. Current Opinion in Neurobiology, 3, 166-170.doi:10.1016/09594388(93)90205-D
80. Saksida, L. M. (2009). Remembering Outside the Box. Science, 325(5936), 40-41.doi:10.1126/science.1177156
81. Saksida, L. M., & Bussey, T. J. (2010). The Representational-Hierarchical View of Amnesia: Translation from Animal to Human. Neuropsychologia, 48(8), 2370-2384.doi:10.1016/j.neuropsychologia.2010.02.026
82. Scoville, W. B., & Milner, B. (1957). Loss of recent memory after bilateral hippocampal lesions. Journal of Neurology, Neurosurgery, and Psychiatry, 20, 11-21.doi:10.1136/jnnp.20.1.11
83. Sejnowski, T. J., Koch, C., & Churchland, P. S. (1988). Computational Neuroscience. Science, 241(4871), 1299-1306.doi:10.1126/science.3045969
84. Shallice, T. (1988). From neuropsychology to mental structure. New York: Cambridge University Press.
85. Shrager, Y., Gold, J. J., Hopkins, R. O., & Squire, L. R. (2006). Intact visual perception in memory-impaired patients with medial temporal lobe lesions. The Journal of Neuroscience, 26(8), 2235-2240. doi:10.1523/JNEUROSCI.4792-05.2006
86. Squire, L. R., Stark, C. E., & Clark, R. E. (2004). The medial temporal lobe. Annual Review of Neuroscience, 27, 279-306.doi:10.1146/annurev.neuro.27.070203.144130
87. Squire, L. R., & Zola-Morgan, S. (1983). The neurology of memory: The case for correspondence between the findings for human and nonhuman primate. In The physiological basis of memory (pp. 199-267). Academic Press.
88. Squire, L. R., & Zola-Morgan, S. M. (1991). The medial temporal lobe memory system. Science, 253, 1380-1386.doi:10.1126/science.1896849
89. Stark, C. E., & Squire, L. R. (2000). Intact visual perceptual discrimination in humans in the absence of perirhinal cortex. Learning & Memory (Cold Spring Harbor, N.Y.), 7(5), 273-278.doi:10.1101/lm.35000
90. Suzuki, W. A. (2009). Perception and the medial temporal lobe: evaluating the current evidence. Neuron, 61(5), 657-666.doi:10.1016/j.neuron.2009.02.008
91. Suzuki, W. A., & Baxter, M. G. (2009). Memory, perception, and the medial temporal lobe: a synthesis of opinions. Neuron, 61(5), 678-679. doi:10.1016/j.neuron.2009.02.009
92. 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. The Journal of Neuroscience, 13, 2430-2451.
93. Tanaka, K., Saito, H., Fukada, Y., & Moriya, M. (1991). Coding Visual Images of Objects in the Inferotempral Cortex of the Macaque Monkey. Journal of Neurophysiology, 66(1), 170-189.
94. Tulving, E., & Schacter, D. L. (1990). Priming and human memory systems. Science, 247(4940), 301-306.doi:10.1126/science.2296719
95. Tyler, L. K., Stamatakis, E. A., Bright, P., Acres, K., Abdallah, S., & Rodd, J. M. (2004). Processing objects at different levels of specificity. Journal of Cognitive Neuroscience, 16(3), 351-362. doi:10.1162/089892904322926692
96. Ullman, S., Vidal-Naquet, M., & Sali, E. (2002). Visual features of intermediate complexity and their use in classification. Nature Neuroscience, 5(7), 682-687.
97. van Strien, N. M., Scholte, H. S., & Witter, M. P. (2008). Activation of the human medial temporal lobes by stereoscopic depth cues. NeuroImage, 40(4), 1815-1823.doi:10.1016/j.neuroimage.2008.01.046
98. Warrington, E., & James, M. (1991). The Visual Object and Space Perception Battery. Bury St Edmunds, UK: Thames Valley Test Company.
99. Warrington, E. K., & Weiskrantz, L. (1968). New method of testing long-term retention with special reference to amnesic patients. Nature, 217(132), 972-974.doi:10.1038/217972a0
100. Wilson, M., & Kaufman, H. M. (1969). Effect of inferotemporal lesions upon processing of visual infomation in monkeys. Journal of Comparative and Physiological Psychology, 69(1), 44-48. doi:10.1037/h0027923
101. Wilson, M., Zieler, R. E., Lieb, J. P., & Kaufman, H. M. (1972). Visual Identification and Memory in Monkeys with Circumscribed Inferotemporal Lesions. Journal of Comparative and Physiological Psychology, 78(2), 173.doi:10.1037/h0032819
102. Winters, B. D., Forwood, S. E., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004). Double dissociation between the effects of peri-postrhinal cortex and hippocampal lesions on tests of object recognition and spatial memory: heterogeneity of function within the temporal lobe. The Journal of Neuroscience, 24(26), 5901-5908.doi:10.1523/JNEUROSCI.1346-04.2004
103. Zhang, L., & Cottrell, G. (2005). Holistic processing develops because it is good. Paper presented at the Proceedings of the 27th Annual Cognitive Science Conference, Stresa, Italy.