Concurrent task effects on memory encoding and retrieval: Further support for an asymmetry

Several studies have demonstrated that divided attention at encoding significantly reduces memory performance, whereas divided attention at retrieval affects memory performance only minimally. However, the possibility exists that retrieval processes have shown such resilience because the concurrent tasks used have often not been very demanding. To assess this possibility, we used independent manipulations of the concurrent task during either encoding or retrieval that included stimulus-response compatibility and participant- versus experimenter-controlled pace. In addition, we manipulated the distribution of practice that the participants received with the primary and the concurrent tasks. The results replicated and extended those recently reported by Rohrer and Pashler (2003), indicating that although memory performance is negatively affected by divided attention at retrieval, especially with noncompatible stimulus-response mapping in the concurrent task, this effect was much smaller than that at encoding, in line with the asymmetry notion. Furthermore, experimenter versus participant control of the concurrent task had no effect on memory retrieval. Finally, under conditions of equal practice with both the memory and the concurrent tasks, memory retrieval was affected only to a small degree. In contrast to encoding processes, the processes involved in retrieval accuracy appear, in many cases, to be less interrupted by divided attention, although this protection requires substantial resources.     

Stress and memory: opposing effects of glucocorticoids on memory consolidation and memory retrieval

It is well established that glucocorticoid hormones, secreted by the adrenal cortex after a stressful event, influence cognitive performance. Some studies have found glucocorticoid-induced memory enhancement. However, many studies have reported impairing effects of glucocorticoids on memory function. This paper reviews recent findings from this laboratory on the acute effects of glucocorticoids in rats on specific memory phases, i.e., memory consolidation and memory retrieval. The evidence suggests that the consequences of glucocorticoid activation on cognition depend largely on the different memory phases investigated. Posttraining activation of glucocorticoid-sensitive pathways involving glucocorticoid receptors enhances memory consolidation in a pattern highly similar to that previously described for adrenal catecholamines. Also, similar to catecholamine effects on memory consolidation, glucocorticoid influences on memory consolidation depend on noradrenergic activation of the basolateral complex of the amygdala and interactions with other brain regions. By contrast, memory retrieval processes are usually impaired with high circulating levels of glucocorticoids or following infusions of glucocorticoid receptor agonists into the hippocampus. The hypothesis is proposed that these apparently dual effects of glucocorticoids on memory consolidation and memory retrieval might be related and that the basolateral complex of the amygdala is a key structure in a memory-modulatory system that regulates, in concert with other brain regions, stress and glucocorticoid effects on both memory consolidation and memory retrieval.     

Behavioral manipulation of retrieval in a spatial memory task for Drosophila melanogaster

A paradigm for operant conditioning of freely walking single Drosophila flies has been described previously. A fly can be conditioned to avoid one side of a small test chamber if the chamber is heated whenever the fly enters this side. In a subsequent memory test without heat the fly continues to avoid the previously heat-associated side. In this experimental design one cannot exclude that flies mark the heated side by an odor that they subsequently avoid during the test. As a final proof for associative learning in the present experiment, flies are trained in one chamber and tested for learning in another, similar one. Handling in the transfer experiment interferes with memory display, even if the fly is returned to the old chamber instead of a new one. Memory can be reactivated, however, by subjecting the fly to an additional brief training (priming), which is too short to establish significant learning in naive flies. For efficient priming, heat has to be applied to the same side as during training in the old chamber. Only then the fly subsequently shows a side preference and avoids the side of the new chamber, which in the old one had been associated with heat. The two chambers are similar but not identical The transfer experiment therefore raises the question as to what the flies use as spatial reference during training and test. In the light, they can be shown to orientate according to visual landmarks associated with the chamber. In complete darkness, where training and memory scores do not differ from those in the light, they are assumed to use a combination of tactile and idiothetic information for orienting.     

The influence of one memory retrieval on a subsequent memory retrieval

Ss produced an instance of a category and following zero or two intervening items produced a second instance of the same category. The second instance was produced more quickly than the initial instance. This finding, in conjunction with other data reported in the paper, indicate that the reduction in latency for the second instance is due mostly to a reduction in the rate with which the category is searched.     

Glucocorticoid-mediated effects of systemic oxytocin upon memory retrieval

During the last decade, a considerable amount of evidence has accumulated to show that oxytocin (OT) is involved with functions other than its classical roles in reproduction-associated processes, such as social recognition, maternal behavior and neuroendocrine regulation of the stress response. It has been shown, for instance, that post-training systemic administration of oxytocin in mice produces an amnestic effect on the step-through inhibitory avoidance. Since it is still unclear how systemic levels of OT may affect CNS memory processes, our aim here was to investigate the hypothesis that systemic OT effects on memory retrieval might be mediated through an oxytocin-induced decrease in glucocorticoid release. In our first experiment, we have found an amnestic effect of i.p. pre-test 0.4 microg/kg of OT upon memory retrieval in the inhibitory avoidance task (IA); this OT dose was shown to (a) significantly decrease plasma corticosterone levels when compared to the saline group, and (b) not to cause any anxiety effects by itself in a plus-maze task. At last, an ineffective-by-itself dose of dexamethasone was able to reverse the amnestic effect of this OT dose. Our results suggest that the amnestic effect of systemically administered oxytocin upon memory retrieval in the inhibitory avoidance task was probably caused by an oxytocin-induced decrease in glucocorticoid release from the adrenal gland.     

Mood-dependent retrieval in visual long-term memory: dissociable effects on retrieval probability and mnemonic precision

Although memories are more retrievable if observers’ emotional states are consistent between encoding and retrieval, it is unclear whether the consistency of emotional states increases the likelihood of successful memory retrieval, the precision of retrieved memories, or both. The present study tested visual long-term memory for everyday objects while consistent or inconsistent emotional contexts between encoding and retrieval were induced using background grey-scale images from the International Affective Picture System (IAPS). In the study phase, participants remembered colours of sequentially presented objects in a negative (Experiment 1a) or positive (Experiment 2a) context. In the test phase, participants estimated the colours of previously studied objects in either negative versus neutral (Experiment 1a) or positive versus neutral (Experiment 2a) contexts. Note, IAPS images in the test phase were always visually different from those initially paired with the studied objects. We found that reinstating negative context and positive context at retrieval resulted in better mnemonic precision and a higher probability of successful retrieval, respectively. Critically, these effects could not be attributed to a negative or positive context at retrieval alone (Experiments 1b and 2b). Together, these findings demonstrated dissociable effects of emotion on the quantitative and qualitative aspects of visual long-term memory retrieval.     

Effects of age and a divided attention task presented during encoding and retrieval on memory

The present studies were designed to examine age differences in memory when attention was divided during encoding, retrieval, or at both times. In Experiment 1, Ss studied categorized words while performing a number-monitoring task during encoding, retrieval, or at both times. Older Ss' free recall and clustering performance declined more than that of young Ss when attention was divided at encoding, but there was no similar age interaction when divided attention occurred at retrieval. In Experiment 2, the task demands at retrieval were increased by using a fast-paced, cued-recall task. The results remained unchanged from Experiment 1. Again, an age interaction occurred with divided attention at encoding but not at retrieval. These results were unexpected, given the emphasis in the memory-aging literature on increased difficulty of retrieval by older adults. The findings pose difficulties for limited processing resource views of age differences in memory.     

Timing matters: Temporal dynamics of stress effects on memory retrieval

Stress may impair memory retrieval. This retrieval impairment has been attributed to the action of the stress hormone cortisol, which is released with a delay of several minutes after a stressful encounter. Hence, most studies tested memory retrieval 20–30 min after stress, when the stress-induced cortisol increase peaks. In the present experiment, we investigated whether retrieval impairments can also be found at later intervals after stress. To this end, participants learned a list of words on day 1. Twenty-four hours later, they were first exposed to a stressor or a nonstressful control manipulation and completed a recognition test for the words either immediately thereafter, 25 min later, or 90 min later. Our findings showed that stress did not impair memory retrieval when memory was tested immediately after the stressor, before cortisol levels were elevated. However, retrieval performance was impaired 25 min after stress, when cortisol levels peaked, as well as 90 min after the stressor, when cortisol levels had already returned to baseline. The retrieval impairment 90 min after stress appeared to be even stronger than the one after 25 min. These findings suggest that the detrimental effects of stress on retrieval performance may last longer than is usually assumed.     

Training and transfer effects of long-term memory retrieval training

ABSTRACT

Long-term memory retrieval ability and working memory can share attention control ability. Based on cognitive plasticity, a hypothesis that cognitive training could improve long-term memory retrieval efficiency and that this could transfer to retrieval involving working memory was proposed. 60 undergraduates were randomly assigned to a group of training and an active control group; all the participants completed the same tasks in the same order before and after the training, the tasks included a long-term memory retrieval access task, a intelligence test, a switching task, a working memory updating task, a response inhibition task and an interference control task. The statistics results indicate that cognitive training can improve long-term memory retrieval efficiency and has a transfer effect on working memory updating, interference control and switching ability, but not on response inhibition or intelligence. This reveal the plasticity of long-term memory retrieval and its influence on working memory.     

Modality effects in retrieval of information from short-term memory

Retrieval from short-term memory was studied in a reaction time task, Ss decided whether or not a target item was present in a memorized list. When modality of presentation was manipulated, fastest reaction times resulted if the target item and all memory items were presented auditorily. All conditions involving pure visual presentation or mixed auditory-visual presentation resulted in reaction times which were longer than those for the pure auditory conditions out which did not differ from each other. This suggests that retrieval can be trom either a precategorical auditory memory or a postcategorical memory which does not preserve the sensory features of the memorized material.     

Theta oscillations predict the detrimental effects of memory retrieval

Retrieving a target item from episodic memory typically enhances later memory for the retrieved item but causes forgetting of competing irrelevant memories. This finding is termed retrieval-induced forgetting (RIF) and is assumed to be the consequence of an inhibitory mechanism resolving retrieval competition. In the present study, we examined brain oscillatory processes related to RIF, as induced by competitive memory retrieval. Contrasting a competitive with a noncompetitive retrieval condition, we found a stronger increase in early evoked theta (4–7 Hz) activity, which specifically predicted RIF, but not retrieval-induced enhancement. Within the cognitive framework of RIF, these findings suggest that theta oscillations reflect arising interference and its resolution during competitive retrieval in episodic memory. Supplemental materials for this article may be downloaded from http://cabn.psychonomic-journals.org/content/supplemental.     

Concurrent and retroactive interference effects in memory of movement patterns

Three experiments examined memory for enacted and observed movement patterns. The effect of visuo-spatial tracing tasks requiring overt motor movements, comparable to those required by the to-be-recalled movement pattern task when enacted, were compared with the effects of non-motor interference tasks, such as articulatory suppression and counting backwards. None of the experiments was able to detect indices of motor mechanisms in memory of movement patterns. The results are discussed in terms of theories of action memory and working memory and of a problem-solving account.     

The effects of load variability in short-term memory task

Six groups of Ss viewed briefly exposed arrays of letters, half designated high-valued and half low-valued. Immediately after each exposure Ss wrote down as many of the stimuli as they could remember. For three groups, the number of letters in each exposure was constant from trial to trial; for the remaining three groups, the number of letters in each exposure varied from trial to trial. This tested the hypothesis that load variability influences the development of an efficient response strategy which, in turn, affects the processing of information stored in short-term memory. The data supported this hypothesis. Performance was superior under the constant load condition due to the ability of these Ss to correctly report both high- and low-valued letters. Poor performance was observed under the variable load condition because of a decrease in the number of low valued letters correctly reported.     

Prospective memory and aging: The effects of working memory and prospective memory task load

Abstract

A person's level of engagement in other actions may influence whether a prospective action is correctly performed. This study used a computerized prospective memory task in which participants remembered to perform an action when a specified background pattern appeared while they simultaneously performed a verbal working memory task. Amount of engagement in the working memory task was manipulated by increasing the number of words to be recalled. Prospective memory load was manipulated by varying the number of prospective targets. Older adults performed more poorly than younger adults on the prospective memory task under higher working memory load and also higher prospective load. Participants with lower working memory load performed better on the prospective task, regardless of age. There were no significant age differences in the absolute accuracy of performance postdictions (post experiment performance awareness). Age differences were also found with a second prospective memory task in which participants were told to write the day of the week (DOW) on the top of answer sheets for tasks performed later in the experiment. No significant correlations were observed between the two prospective memory tasks for either age group.     

Age and task effects in short-term memory of children

Children of 4, 8, and 14 years performed a visual memory task with easy- or hard-to-label displays and with or without repetition of stimuli over trials. Eight pictures were displayed in serial order, and the task was to find the card in the array that matched an identical probe card. Performance improved with age, and strong serial position effects were obtained for all ages and tasks. In contrast to previous studies, primacy effects were obtained for the youngest children tested. Task difficulty increased with difficulty of labeling and with repetition, but order of task difficulty remained the same for all ages. The d’ measure, borrowed from signal detection theory, revealed differences in criterion levels over serial position, which in earlier studies had been confounded with strength of memory.     

Habituation to irrelevant speech: effects on a visual short-term memory task

The Baddeley and Hitch (1974) formulation of short-term or working memory embodied a phonological store within the articulatory loop component of the model. Later formulations specifically postulated an acoustic filter that endowed only speech-like stimuli with obligatory access to this phonological store. This paper presents evidence that this phonological store may have two filters, one of which is subject to habituation and can therefore attenuate the entry of irrelevant speech, thus undermining the obligatory access assumption of the model. An experiment is reported in which subjects were presented with a habituation period comprising 20 min of irrelevant speech--speech to be ignored by the subject--before a test phase in which a visually presented serial recall task with concurrent irrelevant speech was performed. The effect of irrelevant speech, which impairs performance on the primary task when there is no habituation phase, is reduced markedly in those conditions where the speech used in the habituation phase is the same as that used in the test phase, if the irrelevant speech is in a language different from that presented during the subsequent trials or if the habituator is a hummed version of the irrelevant speech passage. When a nonspeech sound (pink noise) is used in the habituation phase, a large irrelevant speech effect is found in the test phase. Morris, Quayle, and Jones (1989) found that humming did not produce an irrelevant speech effect, which suggests that the first filter is permeable to humming but that the second filter is not.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effects of task instructor status on prospective memory performance in preschoolers

The present study applied a 2 × 2 experimental design to assess prospective memory (PM) development across preschool age and to examine the effect of task instructor status (researcher vs. significant other) on PM performance in 80 preschool children. Participants were required to name pictures (ongoing task [OT]), and to remember to refrain from naming but instead give a different response to certain target cues (PM task). Although the OT was of comparable difficulty for both age groups (as indicated by no performance differences), results still indicated significantly higher PM performance in 5-year-olds than in 3-year-olds, confirming the age-related increase of PM capacities between 3 and 5 years. Furthermore, results showed a performance-enhancing effect of significant others as task instructors on both age-groups. Post-hoc analysis revealed that 3-year-olds instructed by a significant other still performed marginally worse than 5-year-olds instructed by a researcher, underlining the finding that substantial changes of PM capacities take place during early childhood.     

Olfactory working memory: effects of verbalization on the 2-back task

Working memory for odors, which has received almost no attention in the literature, was investigated in two experiments. We show that performance in a 2-back task with odor stimuli is well above chance. This is true not only for highly familiar odors, as has been shown by Dade, Zatorre, Evans, and Jones-Gotman, NeuroImage, 14, 650–660, (2001), but also for unfamiliar ones that are notoriously difficult to name. We can conclude that information about an olfactory stimulus can be retained in the short term and can continuously be updated for comparison with new olfactory probes along the lines of a functional odor working memory. However, the performance in the working memory task is highly dependent on participants’ verbalization of the odor. In addition, results indicated that odor working memory performance is dependent on the ability to discriminate among the odor stimuli (Experiment 2). The results are discussed in relation to recent ideas of a separate olfactory working memory slave system.     

Experimentally manipulating the effects of involuntary conscious memory on a priming task

Recent studies showed that involuntary conscious memory can enhance priming in implicit tasks. However, because the results of these studies were based on post hoc selection methods in which subjects were assigned to conditions (aware or unaware) based on their responses on a posttest questionnaire, it is possible that subject selection effects may have influenced the results. The present study used a novel method that experimentally manipulated the effects of involuntary conscious memory on a word stem task. This was accomplished by inducing the experience of word recollection in one test condition while inhibiting it in another. This study showed that subjects who experienced word recollection showed significantly higher rates of priming than those who did not. The results represent the first purely experimental demonstration of involuntary conscious memory's ability to affect priming on implicit tasks.     

Reward schedule effects in extinction: Intertrial interval, memory, and memory retrieval

Rats were trained in a runway such that partial reward occurred on Trial 1 of the day and consistent reward on subsequent massed trials (Group PRT1), or consistent reward occurred on Trial 1 of the day and partial reward on subsequent massed trials (Group PRTM). Under spaced (24-hr) extinction, Group PRT1 was more resistant to extinction than Group PRTM and under massed (1-min) extinction, Group PRTM was more resistant to extinction than Group PRT1. These findings suggest that (a) distinctive stimuli are associated with Trial 1 of the day and with subsequent massed trials, (b) these distinctive stimuli function as retrieval cues for memories, memory retrieval being independent of intertrial interval, and (c) behavior in extinction is controlled by a stimulus compound consisting of the memory of nonreward plus stimuli which accompany the memory of nonreward on rewarded acquisition trials.