How does running memory span work?

In running memory span, a list ends unpredictably, and the last few items are to be recalled. This task is of increasing importance in recent research. We argue that there are two very different strategies for performing running span tasks: a low-effort strategy in which items are passively held until the list ends, when retrieval into a capacity-limited store takes place; and a higher-effort strategy in which working memory is continually updated using rehearsal processes during the list presentation. In two experiments, we examine the roles of these two strategies and the consequences of two types of interference.     

How does running memory span work?

In running memory span, a list ends unpredictably, and the last few items are to be recalled. This task is of increasing importance in recent research. We argue that there are two very different strategies for performing running span tasks: a low-effort strategy in which items are passively held until the list ends, when retrieval into a capacity-limited store takes place; and a higher-effort strategy in which working memory is continually updated using rehearsal processes during the list presentation. In two experiments, we examine the roles of these two strategies and the consequences of two types of interference.     

How much does the human medial gastrocnemius muscle contribute to ankle torques outside the sagittal plane?

Ankle movements in the frontal plane are less prominent though not less relevant than movements in the plantar or dorsal flexion direction. Walking on uneven terrains and standing on narrow stances are examples of circumstances likely imposing marked demands on the ankle medio-lateral stabilization. Following our previous evidence associating lateral bodily sways in quiet standing to activation of the medial gastrocnemius (MG) muscle, in this study we ask: how large is the MG contribution to ankle torque in the frontal plane? By arranging stimulation electrodes in a selective configuration, current pulses were applied primarily to the MG nerve branch of ten subjects. The contribution of populations of MG motor units of progressively smaller recruitment threshold to ankle torque was evaluated by increasing the stimulation amplitude by fixed amounts. From smallest intensities (12–32 mA) leading to the firstly observable MG twitches in force-plate recordings, current pulses reached intensities (56–90 mA) below which twitches in other muscles could not be observed from the skin. Key results showed a substantial MG torque contribution tending to rotate upward the foot medial aspect (ankle inversion). Nerve stimulation further revealed a linear relationship between the peak torque of ankle plantar flexion and inversion, across participants (Pearson R > .81, p < .01). Specifically, regardless of the current intensity applied, the peak torque of ankle inversion amounted to about 13% of plantar flexion peak torque. Physiologically, these results provide experimental evidence that MG activation may contribute to stabilize the body in the frontal plane, especially under situations of challenged stability.     

How does imagery in interactive consumption lead to false memory? A reconstructive memory perspective

Consumers are often exposed to information that may contradict their consumption experience, leading to “false memory” for aspects of the consumption. We develop a theory suggesting why false memory may be heightened due to imagery processing. We subject this theory to a rigorous test in three experiments. We find that post-consumption imagery makes it more difficult to discern between consumption and misleading information thereby boosting false recall. Yet, imagery that is more consumption-based helps reduce consumers' susceptibility to false memory. Consistent with this notion, we explicate the role that attention plays at different stages of consumption in affecting false memory.     

How much memory does oculomotor search have?

Research has demonstrated that oculomotor visual search is guided by memory for which items or locations within a display have already been inspected. In the study reported here, we used a gaze-contingent search paradigm to examine properties of this memory. Data revealed a memory buffer for search history of three to four items. This buffer was effected in part by a space-based trace attached to a location independently of whether the object that had been seen at that position remained visible, and was subject to interference from other stimuli seen in the course of a trial.     

How does acoustic similarity influence short-term memory?

This study attempts to discover why items which are similar in sound are hard to recall in a short-term memory situation. The input, storage, and retrieval stages of the memory system are examined separately. Experiments I, II and III use a modification of the Peterson and Peterson technique to plot short-term forgetting curves for sequences of acoustically similar and control words. If acoustically similar sequences are stored less efficiently, they should be forgotten more rapidly. All three experiments show a parallel rate of forgetting for acoustically similar and control sequences, suggesting that the acoustic similarity effect does not occur during storage. Two input hypotheses are then examined, one involving a simple sensory trace, the other an overloading of a system which must both discriminate and memorize at the same time. Both predict that short-term memory for spoken word sequences should deteriorate when the level of background noise is increased. Subjects performed both a listening test and a memory test in which they attempted to recall sequences of five words. Noise impaired performance on the listening test but had no significant effect on retention, thus supporting neither of the input hypotheses. The final experiments studied two retrieval hypotheses. The first of these, Wickelgren's phonemic-associative hypotheses attributes the acoustic similarity effect to inter-item associations. It predicts that, when sequences comprising a mixture of similar and dissimilar items are recalled, errors should follow acoustically similar items. The second hypothesis attributes the effect to the overloading of retrieval cues which consequently do not discriminate adequately among available responses. It predicts maximum error rate on, not following, similar items. Two experiments were performed, one involving recall of visually presented letter sequences, the other of auditorily presented word sequences. Both showed a marked tendency for errors to coincide with acoustically similar items, as the second hypothesis would predict. It is suggested that the acoustic similarity effect occurs at retrieval and is due to the overloading of retrieval cues.     

How do the internal details of the object contribute to recognition?

Object recognition becomes difficult when the main axis of the object is foreshortened. It has previously been reported that this so-called foreshortened disadvantage is larger when the silhouette of the object is presented than when the line drawing of the object is presented. The pronounced foreshortened disadvantage in silhouette recognition indicates that the internal details of the object, which are absent in the silhouette, provide useful information, particularly when the main axis is foreshortened. But the role of these internal details remains controversial. One account for the pronounced disadvantage is that the internal details contribute to the derivation of the main axis. The other account is that internal details provide the distinctive features that are directly matched to the object represented in memory. The aim in the present study was to determine which of these two explanations best accounts for the differential foreshortened disadvantage between line drawings and silhouettes. To reduce the uncertainty regarding the axis orientation, a 3-D arrow indicating the orientation of the main axis was presented as a cue before the object itself was presented. As a result, the difference in the foreshortened disadvantage between silhouettes and line drawings disappeared. This indicated that the pronounced foreshortened disadvantage for silhouettes was caused by a lack of axis information. In other words, the internal details provided the information necessary for axis derivation when the axis was foreshortened.     

How does the severity of a learning disability affect working memory performance?

Working memory performance was examined in children aged 11-12 years who had borderline, mild, and moderate learning disabilities. Comparisons with children of average abilities were used to determine whether those with more severe learning disabilities had greater impairments in working memory. Seven measures of working memory span were used to assess temporary phonological short-term storage (digit span, word span), temporary visuo-spatial short-term storage (pattern span, spatial span), and temporary short-term storage with additional processing, or central executive, demands (listening span, odd one out span, reverse digit span). Children with mild and moderate learning disabilities were impaired on all measures of working memory compared to children of average abilities. Children with borderline learning disabilities were just as good as children with average abilities on visuo-spatial and complex span tasks, but showed an impairment on phonological span tasks. Children with moderate learning disabilities were indistinguishable from children with mild learning disabilities on simple span tasks, but were significantly poorer than the mild group on the more demanding complex span tasks. For the group as a whole, working memory was strongly related to mental age.     

How does the severity of a learning disability affect working memory performance?

Working memory performance was examined in children aged 11-12 years who had borderline, mild, and moderate learning disabilities. Comparisons with children of average abilities were used to determine whether those with more severe learning disabilities had greater impairments in working memory. Seven measures of working memory span were used to assess temporary phonological short-term storage (digit span, word span), temporary visuo-spatial short-term storage (pattern span, spatial span), and temporary short-term storage with additional processing, or central executive, demands (listening span. odd one out span, reverse digit span). Children with mild and moderate learning disabilities were impaired on all measures of working memory compared to children of average abilities. Children with borderline learning disabilities were just as good as children with average abilities on visuo-spatial and complex span tasks, but showed an impairment on phonological span tasks. Children with moderate learning disabilities were indistinguishable from children with mild learning disabilities on simple span tasks, but were significantly poorer than the mild group on the more demanding complex span tasks. For the group as a whole, working memory was strongly related to mental age.     

How does background information improve memory for text content?

In two experiments, we investigated whether reading background information benefits memory for text content by influencing the amount of content encoded or the organization of the encoded content. In Experiment 1, half of the participants read background information about the issues to be discussed in the text material, whereas half did not. All the participants were then tested for free recall and cued recall of text content. Free recall was greater for individuals who read issue information than for those who did not. The groups did not differ on cued recall, suggesting that background information did not facilitate the encoding of more text content. Measures of representational organization indicated that increased recall in the issue information group resulted from better organization of content in memory. Experiment 2 extended these findings, using background information about text sources, demonstrated that the efficacy of background information depends on the semantic relationship between that information and text content.     

Eye movements and serial memory for visual-spatial information: does time spent fixating contribute to recall?

This research investigated the nature of encoding and its contribution to serial recall for visual-spatial information. In order to do so, we examined the relationship between fixation duration and recall performance. Using the dot task--a series of seven dots spatially distributed on a monitor screen is presented sequentially for immediate recall--performance and eye-tracking data were recorded during the presentation of the to-be-remembered items. When participants were free to move their eyes at their will, both fixation durations and probability of correct recall decreased as a function of serial position. Furthermore, imposing constant durations of fixation across all serial positions had a beneficial impact (though relatively small) on item but not order recall. Great care was taken to isolate the effect of fixation duration from that of presentation duration. Although eye movement at encoding contributes to immediate memory, it is not decisive in shaping serial recall performance. Our results also provide further evidence that the distinction between item and order information, well-established in the verbal domain, extends to visual-spatial information.     

Does the thought of death contribute to the memory benefit of encoding with a survival scenario?

Four studies tested whether the thought of death contributes to the survival processing advantage found in memory tests (i.e., the survival effect). In the first study, we replicated the “Dying To Remember” (DTR) effect identified by Burns and colleagues whereby activation of death thoughts led to better retention than an aversive control situation. In Study 2, we compared an ancestral survival scenario, a modern survival scenario and a “life-after-death” scenario. The modern survival scenario and the dying scenario led to higher levels of recall than the ancestral scenario. In Study 3, we used a more salient death-thought scenario in which people imagine themselves on death row. Results showed that the “death-row” scenario yielded a level of recall similar to that of the ancestral survival condition. We also collected ratings of death-related thoughts (Studies 3 and 4) and of survival-related and planning thoughts (Study 4). The ratings indicated that death-related thoughts were induced more by the dying scenarios than by the survival scenarios, whereas the reverse was observed for both survival-related and planning thoughts. The findings are discussed in the light of two contrasting views of the influence of mortality salience in the survival effect.     

How does repetition affect memory? Evidence from judgments of recency

Four experiments were done to investigate the effects of repetition on judgment of recency (JOR). Experiment 1 showed that repetition can make an item seem either more recent or less recent than a nonrepeated item, depending on presentation spacing. Experiments 2-4 showed that subjects are able to judge the recency of a repeated item’s first presentation or of its second presentation with a high degree of independence, especially if they report that the item occurred twice. The data are more consistent with an independent-trace explanation of JOR and repetition than with a cumulative-strength account, but neither hypothesis explains how repetition can make an item seem less recent. It is proposed that the findings as a whole can be better explained by a hypothesis based on recursive reminding.     

How does it feel to act together?

This paper on the phenomenology of joint agency proposes a foray into a little explored territory at the intersection of two very active domains of research: joint action and sense of agency. I explore two ways in which our experience of joint agency may differ from our experience of individual agency. First, the mechanisms of action specification and control involved in joint action are typically more complex than those present in individual actions, since it is crucial for joint action that people coordinate their plans and actions. I discuss the implications that these coordination requirements might have for the strength of the sense of agency an agent may experience for a joint action. Second, engagement in joint action may involve a transformation of agentive identity and a partial or complete shift from a sense of self-agency to a sense of we-agency. I discuss several factors that may contribute to shaping our sense of agentive identity in joint action.     

How does encoding context affect memory in younger and older adults?

How does encoding context affect memory? Participants studied visually presented words viewed concurrently with a rich (intact face) or weak (scrambled face) image as context and subsequently made “Remember”, “Know”, or “New” judgements to words presented alone. In Experiment 1a, younger, but not older, adults showed higher recollection accuracy to words from rich- than from weak-context encoding trials. The age-related deficit in recollection occurred, in Experiment 1b, even when encoding and retrieval time was doubled in older adults, suggesting that insufficient processing time cannot account for this age-related deficit. In Experiment 1c, dividing attention in young, during encoding, reduced overall memory, though the recollection boost from rich encoding contexts remained, suggesting that reduced attention resources cannot explain this age-related deficit. Experiment 2 showed that an own-age bias, to face images as context, could not explain the age-related differences either. Results suggest that age deficits in recollection stem from a lack of spontaneous binding, or elaboration, of context to target information during encoding.     

How does encoding context affect memory in younger and older adults?

How does encoding context affect memory? Participants studied visually presented words viewed concurrently with a rich (intact face) or weak (scrambled face) image as context and subsequently made "Remember", "Know", or "New" judgements to words presented alone. In Experiment 1a, younger, but not older, adults showed higher recollection accuracy to words from rich- than from weak-context encoding trials. The age-related deficit in recollection occurred, in Experiment 1b, even when encoding and retrieval time was doubled in older adults, suggesting that insufficient processing time cannot account for this age-related deficit. In Experiment 1c, dividing attention in young, during encoding, reduced overall memory, though the recollection boost from rich encoding contexts remained, suggesting that reduced attention resources cannot explain this age-related deficit. Experiment 2 showed that an own-age bias, to face images as context, could not explain the age-related differences either. Results suggest that age deficits in recollection stem from a lack of spontaneous binding, or elaboration, of context to target information during encoding.     

What does it take for context to support action memory?

Previous research on the relation between context and action memory has given ambiguous results. Some experiments have found positive context effects, whereas other experiments have failed to demonstrate a context effect in action memory. Under nonmotor encoding conditions orderly action-locus pairings have been found to yield better recall than random pairings, this not being the case with motor encoding (Helstrup, 1989 a ). Three new experiments explored whether memory for loci could be linked with memory for action–using modified replications. The first experiment provided item-specific reasons for the action-locus connections, whereas the second experiment used a whole-list relational context task. Both experiments indicated that contexts can influence action memory also under enactment conditions, with strongest effect for whole-list contexts. The third experiment demonstrated how a positive context effect can be removed when the functional value of whole-list relational support cues is reduced.     

Does retrieval fluency contribute to the underconfidence-with-practice effect?

Judgments of learning (JOLs) made during multiple study-test trials underestimate increases in recall performance across those trials, an effect that has been dubbed the underconfidence-with-practice (UWP) effect. In 3 experiments, the authors examined the contribution of retrieval fluency to the UWP effect for immediate and delayed JOLs. The UWP effect was demonstrated with reliable underconfidence on Trial 2 occurring for both kinds of JOL. However, in contrast to a retrieval-fluency hypothesis, fine-grained analyses indicated that the reliance of JOLs on retrieval fluency contributed minimally to the UWP effect. Our discussion focuses on the status of the retrieval-fluency hypothesis for the UWP effect.     

How does horizontal and vertical navigation influence spatial memory of multifloored environments?

Although a number of studies have been devoted to 2-D navigation, relatively little is known about how the brain encodes and recalls navigation in complex multifloored environments. Previous studies have proposed that humans preferentially memorize buildings by a set of horizontal 2-D representations. Yet this might stem from the fact that environments were also explored by floors. Here, we have investigated the effect of spatial learning on memory of a virtual multifloored building. Two groups of 28 participants watched a computer movie that showed either a route along floors one at a time or travel between floors by simulated lifts, consisting in both cases of a 2-D trajectory in the vertical plane. To test recognition, the participants viewed a camera movement that either replicated a segment of the learning route (familiar segment) or did not (novel segment—i.e., shortcuts). Overall, floor recognition was not reliably superior to column recognition, but learning along a floor route produced a better spatial memory performance than did learning along a column route. Moreover, the participants processed familiar segments more accurately than novel ones, not only after floor learning, but crucially, also after column learning, suggesting a key role of the observation mode on the exploitation of spatial memory.