Cortical reinstatement and the confidence and accuracy of source memory

NeuroImage

Volumn 109, Issue , 2015, Pages 118-129

  Thakral, Preston P ^a   Wang, Tracy H ^a   Rugg, Michael D ^a  

^a UNIVERSITY OF TEXAS AT DALLAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ANGULAR GYRUS; ARTICLE; AUDITORY MEMORY; AUDITORY THRESHOLD; BRAIN REGION; CONFIDENCE; CONTROLLED STUDY; CORTICAL REINSTATEMENT; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HUMAN; HUMAN EXPERIMENT; MENTAL TASK; NERVOUS SYSTEM FUNCTION; NORMAL HUMAN; OCCIPITAL GYRUS; PARAHIPPOCAMPAL GYRUS; PERSONALITY; POSTERIOR CINGULATE; RETROSPLENIAL CORTEX; TASK PERFORMANCE; VISUAL MEMORY; VISUAL THRESHOLD; ADULT; BRAIN; BRAIN MAPPING; COMPUTER ASSISTED DIAGNOSIS; EPISODIC MEMORY; FEMALE; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSIOLOGY; YOUNG ADULT;

ADULT; BRAIN; BRAIN MAPPING; FEMALE; HUMANS; IMAGE INTERPRETATION, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MALE; MEMORY, EPISODIC; YOUNG ADULT;

EID: 84921472226     PISSN: 10538119     EISSN: 10959572     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2015.01.003     Document Type: Article

References (72)

1. Alvarez P., Squire L.R. Memory consolidation the medial temporal lobe: a simple network model. Proc. Natl. Acad. Sci. U. S. A. 1994, 91:7041-7045.
2. Baddeley A. The episodic buffer: a new component of working memory?. Trends Cogn. Sci. 2000, 4:417-423.
3. Bradley J.V. A nonparametric test for interactions of any order. J. Qual. Technol. 1979, 11:177-184.
4. Chen J., Olsen R.K., Preston A.R., Glover G.H., Wagner A.D. Associative retrieval processes in the human medial temporal lobe: hippocampal retrieval success and CA1 mismatch detection. Learn. Mem. 2011, 18:523-528.
5. Cocosco C.A., Kollokian V., Kwan R.S., Evans A.C. BrainWeb: online interface to a 3D MRI simulated brain database. Proceedings of the Third International Conference on Function Mapping of the Human Brain, Copenhagen, Denmark 1997, (S235 p. S235).
6. Danker J.F., Anderson J.R. The ghosts of brain states past: remembering reactivates the brain regions engaged during encoding. Psychol. Bull. 2010, 136:87-102.
7. Diana R.A., Yonelinas A.P., Ranganath C. Imaging recollection and familiarity in the medial temporal lobe: a three-component model. Trends Cogn. Sci. 2007, 11:379-386.
8. Diana R.A., Yonelinas A.P., Ranganath C. Medial temporal lobe activity during source retrieval reflects information type not memory strength. J. Cogn. Neurosci. 2009, 22:1808-1818.
9. Duarte A., Henson R.N., Graham K.S. Stimulus content and the neural correlates of source memory. Brain Res. 2011, 1373:110-123.
10. Düzel E., Habib R., Rotte M., Guderian S., Tulving E., Heinze H.-J. Human hippocampal and parahippocampal activity during visual associative recognition memory for spatial and nonspatial stimulus configurations. J. Neurosci. 2003, 23:9439-9444.
11. Fisher R.A. Statistical Methods for Research Workers 1950, Oliver and Boyd, London.
12. Friston K.J., Fletcher P., Josephs O., Holmes A., Rugg M.D., Turner R. Event-related fMRI: characterizing differential responses. Neuroimage 1998, 7:30-40.
13. Friston K.J., Penny W., Phillips C., Kiebel S., Hinton G., Ashburner J. Classical and Bayesian inference in neuroimaging: theory. Neuroimage 2002, 16:465-483.
14. Glanzer M., Hilford A., Kim K. Six regularities of source recognition. J. Exp. Psychol. Learn. Mem. Cogn. 2004, 30:1176-1195.
15. Gordon A.M., Rissman J., Kiani R., Wagner A.D. Cortical reinstatement mediates the relationship between content-specific encoding activity and subsequent recollection decisions. Cereb. Cortex 2014, 24:3350-3364.
16. Gottlieb L.J., Uncapher M.R., Rugg M.D. Dissociation of the neural correlates of visual and auditory contextual encoding. Neuropsychologia 2010, 48:137-144.
17. Hayama H.R., Vilberg K.L., Rugg M.D. Overlap between the neural correlates of cued recall and source memory: evidence for a generic recollection network?. J. Cogn. Neurosci. 2012, 24:1127-1137.
18. Hofstetter C., Achaibou A., Vuilleumier P. Reactivation of visual cortex during memory retrieval: content specificity and emotional modulation. Neuroimage 2012, 60:1734-1745.
19. Huijbers W., Pennartz C.M.A., Rubin D.C., Daselaar S.M. Imagery and retrieval of auditory and visual information: neural correlates of successful and unsuccessful performance. Neuropsychologia 2011, 49:1730-1740.
20. Johnson J.D., Rugg M.D. Recollection the reinstatement of encoding-related cortical activity. Cereb. Cortex 2007, 17:2507-2515.
21. Johnson J.D., Minton B.R., Rugg M.D. Content dependence of the electrophysiological correlates of recollection. Neuroimage 2008, 39:406-416.
22. Johnson J.D., McDuff S.G., Rugg M.D., Norman K.A. Recollection, familiarity, and cortical reinstatement: a multivoxel pattern analysis. Neuron 2009, 63:697-708.
23. Johnson J.D., Suzuki S., Rugg M.D. Recollection familiarity and content-sensitivity in lateral parietal cortex: a high-resolution study. Front. Hum. Neurosci. 2013, 7:1-15.
24. Kahn I., Davachi L., Wagner A.D. Functional-neuroanatomic correlates of recollection: implications for models of recognition memory. J. Neurosci. 2004, 24:4172-4180.
25. Kim H. Dissociating the roles of the default-mode dorsal and ventral networks in episodic memory retrieval. Neuroimage 2010, 50:1648-1657.
26. Köhler S., Danckert S., Gati J.S., Menon R.S. Novelty responses to relational and non-relational information in the hippocampus and the parahippocampal region: a comparison based on event-related fMRI. Hippocampus 2005, 15:763-774.
27. Kucera H., Francis W.N. Computational Analysis of Present-day American English 1967, Brown University Press, Providence RI.
28. Kuhl B.A., Rissman J., Chun M.M., Wagner A.D. Fidelity of neural activation reveals competition between memories. Proc. Natl. Acad. Sci. U. S. A. 2011, 108:5903-5908.
29. Kuhl B.A., Johnson M.K., Chun M.M. Dissociable neural mechanisms for goal-directed versus incidental memory reactivation. J. Neurosci. 2013, 33:16099-16109.
30. Lazar N.A., Luna B., Sweeney J.A., Eddy W.F. Combining brains: a survey of methods for statistical pooling of information. Neuroimage 2002, 16:538-550.
31. Loftus G.R., Masson M.E.J. Using confidence intervals in within-subject designs. Psychon. Bull. Rev. 1994, 1:476-490.
32. Mandler G. Recognizing: the judgment of previous occurrence. Psychol. Rev. 1980, 87:252-271.
33. McClelland J.L., McNaughton B.L., O'Reilly R.C. Why there are complementary learning systems in the hippocampus neocortex: insights from the successes and failures of connectionist models of learning and memory. Psychol. Rev. 1995, 102:419-457.
34. McDuff S.G.R., Frankel H.C., Norman K.A. Multivoxel pattern analysis reveals increased memory targeting and reduced use of retrieved details during single-agenda source monitoring. J. Neurosci. 2009, 29:508-516.
35. Mickes L., Wais P.E., Wixted J.T. Recollection is a continuous process: implications for dual-process theories of recognition memory. Psychol. Sci. 2009, 20:509-515.
36. Mitchell K.J., Johnson M.K. Source monitoring 15years later: what have we learned from fMRI about the neural mechanisms of source memory?. Psychol. Bull. 2009, 135:638-677.
37. Morris C.D., Bransford J.D., Franks J.J. Levels of processing versus transfer appropriate processing. J. Verbal Learn. Verbal Behav. 1977, 16:519-533.
38. Norman K.A., O'Reilly R.C. Modeling hippocampal and neocortical contributions to recognition memory: a complementary-learning-systems approach. Psychol. Rev. 2003, 110:611-646.
39. Nyberg L., Habib R., McIntosh A.R., Tulving E. Reactivation of encoding-related brain activity during memory retrieval. Proc. Natl. Acad. Sci. U. S. A. 2000, 97:11120-11124.
40. Parks C.M., Yonelinas A.P. Moving beyond pure signal-detection models: comment on Wixted 2007. Psychol. Rev. 2007, 114:188-202.
41. Qin J., Raye C.L., Johnson M.K., Mitchell K.J. Source memory ROCs are typically curvilinear: comment on Yonelinas 1999. J. Exp. Psychol. Learn. Mem. Cogn. 2001, 27:1110-1115.
42. Ritchey M., Wing E.A., LaBar K.S., Cabeza R. Neural similarity between encoding and retrieval is related to memory via hippocampal interactions. Cereb. Cortex 2013, 23:2818-2828.
43. Roediger H.L., Gallo D.A., Geraci L. Processing approaches to cognition: the impetus from the levels of processing framework. Memory 2002, 10:319-332.
44. Rolls E.T. Memory systems in the brain. Annu. Rev. Psychol. 2000, 51:599-630.
45. Rugg M.D., Vilberg K.L. Brain networks underlying episodic memory retrieval. Curr. Opin. Neurobiol. 2013, 23:255-260.
46. Rugg M.D., Johnson J.D., Park H., Uncapher M.R. Encoding-retrieval overlap in human episodic memory: a functional neuroimaging perspective. Prog. Brain Res. 2008, 169:339-352.
47. Rugg M.D., Vilberg K.L., Mattson J.T., Yu S.S., Johnson J.D., Suzuki M. Item memory context memory and the hippocampus: fMRI evidence. Neuropsychologia 2012, 50:3070-3079.
48. Sawilowsky S.S. Nonparametric tests of interaction in experimental design. Rev. Educ. Res. 1990, 60:91-126.
49. Shastri L. Episodic memory and cortico-hippocampal interactions. Trends Cogn. Sci. 2002, 6:162-168.
50. Slotnick S.D. Rapid retinotopic reactivation during spatial memory. Brain Res. 2009, 1268:97-111.
51. Slotnick S.D. "Remember" source memory ROCs indicate recollection is a continuous process. Memory 2010, 18:27-39.
52. Slotnick S.D., Dodson C.S. Support for a continuous single-process model of recognition memory and source memory. Mem. Cogn. 2005, 33:151-170.
53. Slotnick S.D., Thakral P.P. The hippocampus operates in a threshold manner during spatial source memory. Neuroreport 2013, 24:265-269.
54. Slotnick S.D., Klein S.A., Dodson C.S., Shimamura A.P. An analysis of signal detection and threshold models of source memory. J. Exp. Psychol. Learn. Mem. Cogn. 2000, 26:1499-1517.
55. Squire L.R., Wixted J.T., Clark R.E. Recognition memory and the medial temporal lobe: a new perspective. Nat. Rev. Neurosci. 2007, 8:872-883.
56. Staresina B.P., Henson R.N.A., Kriegeskorte N., Alink A. Episodic reinstatement in the medial temporal lobe. J. Neurosci. 2012, 32:18150-18156.
57. Thakral P.P., Slotnick S.D., Schacter D.L. Conscious processing during retrieval can occur in early and later visual regions. Neuropsychologia 2013, 51:482-487.
58. Tulving E. Elements of Episodic Memory 1983, Oxford University Press, New York.
59. Van Essen D.C. A population-average landmark- and surface-based PALS atlas of human cerebral cortex. Neuroimage 2005, 28:635-662.
60. Vilberg K.L., Rugg M.D. The neural correlates of recollection: transient versus sustained FMRI effects. J. Neurosci. 2012, 32:15679-15687.
61. Vilberg K.L., Rugg M.D. Temporal dissociations within the core recollection network. Cogn. Neurosci. 2014, 5:77-84.
62. Wais P.E., Squire L.R., Wixted J.T. In search of recollection and familiarity signals in the hippocampus. J. Cogn. Neurosci. 2009, 22:109-123.
63. Wheeler M.E., Petersen S.E., Buckner R.L. Memory's echo: vivid remembering reactivates sensory-specific cortex. Proc. Natl. Acad. Sci. U. S. A. 2000, 97:11125-11129.
64. Wimber M., Maaβ A., Staudigl T., Richardson-Klavehn A., Hanslmayr S. Rapid memory reactivation revealed by oscillatory entrainment. Curr. Biol. 2012, 22:1482-1486.
65. Wixted J.T. Dual-process theory and signal-detection theory of recognition memory. Psychol. Rev. 2007, 114:152-176.
66. Wixted J.T., Mickes L. A continuous dual-process model of remember/know judgments. Psychol. Rev. 2010, 117:1025-1054.
67. Wixted J.T., Mickes L., Squire L.R. Measuring recollection familiarity in the medial temporal lobe. Hippocampus 2010, 20:1195-1205.
68. Woodruff C.C., Johnson J.D., Uncapher M.R., Rugg M.D. Content-specificity of the neural correlates of recollection. Neuropsychologia 2005, 43:1022-1032.
69. Worsley K.J., Marrett S., Neelin P., Vandal A.C., Friston K.J., Evans A.C. A unified statistical approach for determining significant signals in images of cerebral activation. Hum. Brain Mapp. 1996, 4:58-73.
70. Yonelinas A.P. The nature of recollection and familiarity: a review of 30 rears of research. J. Mem. Lang. 2002, 46:441-517.
71. Yu S.S., Johnson J.D., Rugg M.D. Hippocampal activity during recognition memory co-varies with the accuracy confidence of source memory judgments. Hippocampus 2012, 22:1429-1437.
72. Yu S.S., Johnson J.D., Rugg M.D. Dissociation of recollection-related neural activity in ventral lateral parietal cortex. Cogn. Neurosci. 2012, 3:142-149.