Abstract

Tests of recognition memory in macaques typically assay memory for objects or isolated images, over time spans of seconds to hours from stimulus presentation, and/or require extensive training. Here, we propose a new application of the flicker change detection task that could measure object-in-scene memory days after single-trial exposures. In three experiments, participants searched for a changing object – or “target” – embedded within a scene as their eye movements were tracked. For new targets-in-scenes, the change is difficult to detect and requires extensive search. Once the target is found, however, the change becomes obvious. We reasoned that the decreased times required to find a target in a repeated scene would indicate memory for the target. In humans, targets were found faster when the targets-and-scenes were explicitly remembered than when they were forgotten, or had never been seen before. This led to faster repeated-trial compared to novel-trial search times. Based solely on repeated-trial search times, we were able to select distributions comprised of predominantly remembered or predominantly forgotten trials. Macaques exhibited the same repetition effects as humans, suggesting that remembered trials could be dissociated from novel or forgotten trials using the same procedures we established in humans. Finally, an anterograde amnesic patient with damage that included the medial temporal lobe (MTL) showed no search time differences, suggesting that memory revealed through search times on this task requires MTL integrity. Together, these findings indicate that the time required to locate a changing object reveals object-in-scene memory over long retention intervals in humans and macaques.

Highlights

  • IntroductionA longheld view is that amnesic patients who show impairments in long-term memory for facts and events that they can consciously recall (explicit/declarative memory) show intact longterm memory for habits/patterns without conscious awareness (implicit/non-declarative memory) and have intact short-term memory (see Squire et al, 1993 for review)

  • Memories are organized into several distinct processes

  • The hippocampus, along with surrounding medial temporal lobe (MTL) structures, has been implicated in the formation of explicit/declarative memories, whereas procedural and implicit memories are generally thought to be mediated by non-MTL structures (Zola-Morgan and Squire, 1993)

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Summary

Introduction

A longheld view is that amnesic patients who show impairments in long-term memory for facts and events that they can consciously recall (explicit/declarative memory) show intact longterm memory for habits/patterns without conscious awareness (implicit/non-declarative memory) and have intact short-term memory (see Squire et al, 1993 for review) According to this view, the hippocampus, along with surrounding medial temporal lobe (MTL) structures, has been implicated in the formation of explicit/declarative memories, whereas procedural and implicit memories are generally thought to be mediated by non-MTL structures (Zola-Morgan and Squire, 1993). An additional distinction may be that the hippocampus plays a timelimited role in memory processing (Squire et al, 1984, but see Nadel and Moscovitch, 1997) Cutting across these accounts, the hippocampus is thought to be important for the formation of long-term relational memory, even when learned over a single exposure, or “episode.”

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