1,081
Views
18
CrossRef citations to date
0
Altmetric
Original Articles

Reward boosts working memory encoding over a brief temporal window

, , &
Pages 291-312 | Received 01 Jun 2014, Accepted 26 Jan 2015, Published online: 06 Mar 2015
 

Abstract

Selection mechanisms for WM are ordinarily studied by explicitly cueing a subset of memory items. However, we might also expect the reward associations of stimuli we encounter to modulate their probability of being represented in working memory (WM). Theoretical and computational models explicitly predict that reward value should determine which items will be gated into WM. For example, a model by Braver and colleagues in which phasic dopamine signalling gates WM updating predicts a temporally-specific but not item-specific reward-driven boost to encoding. In contrast, Hazy and colleagues invoke reinforcement learning in cortico-striatal loops and predict an item-wise reward-driven encoding bias. Furthermore, a body of prior work has demonstrated that reward-associated items can capture attention, and it has been shown that attentional capture biases WM encoding. We directly investigated the relationship between reward history and WM encoding. In our first experiment, we found an encoding benefit associated with reward-associated items, but the benefit generalized to all items in the memory array. In a second experiment this effect was shown to be highly temporally specific. We speculate that in real-world contexts in which the environment is sampled sequentially with saccades/shifts in attention, this mechanism could effectively mediate an item-wise encoding bias, because encoding boosts would occur when rewarded items were fixated.

We thank two anonymous reviewers for their constructive comments.

No potential conflict of interest was reported by the authors.

This research was supported by a Wellcome Trust DPhil Studentship to GW.

We thank two anonymous reviewers for their constructive comments.

No potential conflict of interest was reported by the authors.

This research was supported by a Wellcome Trust DPhil Studentship to GW.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.