September 2018
Volume 18, Issue 10
Open Access
Vision Sciences Society Annual Meeting Abstract  |   September 2018
The efficacy of retroactive control of visual memory encoding depends on preceding oscillatory activities.
Author Affiliations
  • April Pereira
    Department of Psychology, University of Toronto Mississauga
  • Keisuke Fukuda
    Department of Psychology, University of Toronto Mississauga
Journal of Vision September 2018, Vol.18, 830. doi:10.1167/18.10.830
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      April Pereira, Keisuke Fukuda; The efficacy of retroactive control of visual memory encoding depends on preceding oscillatory activities.. Journal of Vision 2018;18(10):830. doi: 10.1167/18.10.830.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Despite the virtually unlimited capacity of visual long-term memory, our ability to encode new visual information into this offline storage fluctuates from moment to moment, thus rendering some information forgotten later in time. Is there any way to monitor this moment-to-moment fluctuation and correct them when needed in real time? Previously we have demonstrated that we can monitor this fluctuation from multiple electroencephalograms (EEG) measures of memory encoding in real time and intervene failed memory encoding by providing re-encoding opportunities for stimuli that were predicted to be poorly encoded by the EEG measures (Fukuda & Woodman, 2015). However, it is unclear whether we can voluntarily change the fate of failed memory encoding without providing re-encoding opportunities. To test this, we recorded participants' EEG while they were sequentially presented with 600 pictures of random objects to remember. Importantly in a third of the trials, a post-stimulus cue was presented to prompt participants to try harder to encode the preceding stimulus. Our results replicated our previous findings that power of occipital alpha (8-14Hz) and frontal theta (5-7Hz) activities during encoding predicted the quality of memory encoding. More importantly, participants successfully upregulated the memory encoding for cued items even when the EEG indices measured prior to the cue onset predicted failed encoding (i.e., strong occipital alpha power and weak frontal theta power). Interestingly, the magnitude of post-stimulus cueing benefit depended on the frontal theta power but not on the occipital alpha power measured prior to the cue onset. More specifically, weak frontal theta power induced larger cueing benefit than strong frontal theta power, but the alpha power did not differentiate the magnitude of cueing benefit. These results not only demonstrate another approach to intervene our failed memory encoding but also suggest dissociative cognitive mechanisms underlying the two EEG indices of memory encoding.

Meeting abstract presented at VSS 2018

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