Repetition and Lag Effects in Movement Recognition

Whether repetition and lag improve the recognition of movement patterns was investigated. Recognition memory was tested for one repetition, two-repetitions massed, and two-repetitions distributed with movement patterns repeated at lags of 3, 5, 7, and 13. Recognition performance was examined both immediately afterwards and following a 48 hour delay. Both repetition and lag effects failed to be demonstrated, providing some support for the claim that memory is unaffected by repetition at a constant level of processing (Craik & Lockhart, 1972). There was, as expected, a significant decrease in recognition memory following the retention interval, but this appeared unrelated to repetition or lag.     

On the differential nature of implicit and explicit memory

In this article, we report two experiments that provide further evidence concerning the differential nature of implicit and explicit memory. In Experiment 1, subjects first undertook a sentenceverification task. While carrying out this task, half of the subjects were also required to carry out a secondary processing task involving tone monitoring. Twenty-four hours later, the subjects’ memory for target items in the sentence-verification task was tested explicitly by means of a recognition task and implicitly by examining the extent to which the items primed fragment completion. Recognition performance was significantly impaired by the imposition of secondary processing demands during the original learning phase. In contrast, fragment completion was completely unaffected by this additional processing, even though substantial priming was observed. In Experiment 2, we examined whether priming in fragment completion is influenced by the nature of repetition during initial learning. Subjects studied a list of target items that were each repeated twice. Halfthe items were repeatedimmediately (lag 0) and halfwere repeated after six intervening items (lag 6). Memory for the itemswas assessed by recognition and by priming in fragment completion. Recognition was affected by lag, with lag 6 items being recognized better than lag 0 items. However, although significant priming was obtained, the extent of this priming was uninfluenced by lag. These data indicate two additional dimensions along which implicit and explicit memory differ and, furthermore, they support recent conceptualizations of processing differences underlying these two forms of memory.     

Memory with and without awareness: performance and electrophysiological evidence of savings.

Event-related potentials (ERPs) recorded on the scalp were shown to be sensitive indicators of the strength of a memory trace on both implicit and explicit tests of memory. In explicit recognition tests, the amplitude of a positive potential identified as P300 was larger for "old" than for "new" words regardless of whether the subject categorized the items correctly. This effect, however, was statistically reliable only when the recognition memory (d') was relatively high. In contrast to ERPs, the reaction times in explicit recognition were sensitive to accuracy but not to repetition. In implicit tests, lexical decisions to repeated words were faster than to newly presented words. The magnitude of the repetition effect varied neither with elapsed time since the last repetition nor with the number of previous repetitions. In contrast, the P300 elicited by the same words were sensitive to both lag and recency of repetition, suggesting that they were influenced by the episodic memory strength of the items.     

The word frequency effect in recognition memory versus repetition priming

The role of word frequency in recognition memory and repetition priming was investigated by using a manipulation of attention. In Experiment 1, the lexical decision task produced greater repetition priming for low-frequency words than for high-frequency words following either the attended or the unattended study condition. The recognition memory test, on the other hand, showed a low-frequency word advantage only following the attended study condition. Furthermore, this advantage was limited to the measure of recognition memory based on conscious recollection of the study episode. In Experiment 2, a speeded recognition memory test replicated the pattern obtained with the unspeeded recognition memory test in Experiment 1. These results argue against the view that the word frequency effects in recognition memory and repetition priming have the same origin. Instead, the results suggest that the word frequency effect in recognition memory has its locus in conscious recollection.     

Repetition effects on word fragment completion: The role of competition among responses

Four experiments examined the effect of spaced repetition of study words on completion of word fragments with only one solution and word fragments with multiple solutions. Recognition was used as test of explicit memory in the first two experiments. The study words were presented either once or three times. Repetition was found to increase recognition memory substantially, and to affect fragment completion performance only marginally. This was true for both single- and multiple-solution fragments, showing that competition among responses is not critical for the magnitude of the repetition effect in fragment completion. This finding, that the repetition effect is marginal also when the type of cues provides an occasion for repetition effects to show up, suggests that the real effect of repetition on perceptual priming is borderline. It is proposed that memory from the first presentation eliminates necessary processing of items when they are re-exposed, and that the repetition effect thereby is reduced.     

How many memory systems? Evidence from aging

The present research tested Tulving's (1985) ternary memory theory. Young (ages 19-32) and older (ages 63-80) adults were given procedural, semantic, and episodic memory tasks. Repetition, lag, and codability were manipulated in a picture-naming task, followed by incidental memory tests. Relative to young adults, older adults exhibited lower levels of recall and recognition, but these episodic measures increased similarly as a function of lag and repetition in both age groups. No age-related deficits emerged in either semantic memory (vocabulary, latency slopes, naming errors, and tip-of-the-tongue responses) or procedural memory (repetition priming magnitude and rate of decline). In addition to the age by memory task dissociations, the manipulation of codability produced slower naming latencies and more naming errors (semantic memory), yet promoted better recall and recognition (episodic memory). Finally, a factor analysis of 11 memory measures revealed three distinct factors, providing additional support for a tripartite memory model.     

Temporal characteristics of visual memory

In order to infer the temporal relations among iconic, short-term, and long-term components of visual memory, random dot patterns were used as memory stimuli in six recognition memory experiments. Experiment 1 demonstrated that recognition was still above chance for intervals up to 12 s. In Experiments 2 and 3, an intervening masking stimulus was found to be effective only if presented within the first 500 ms of the interval. The remaining three experiments employed a two-target task, with the second target replacing the masking stimulus. Recognition performance with the second target was the same as that in a single-target task, whereas performance with the first target was almost at chance level. Increasing the interval between the targets resulted in a gradual improvement in the recognition of the first target.     

Effects of acute stress and GluN2B-containing NMDA receptor antagonism on object and object–place recognition memory

The mechanisms underlying the complex effects of acute stress on memory are incompletely understood. Previous work suggests that the activation of N-methyl-d-aspartate (NMDA) receptors specifically containing GluN2B subunits may underlie the disruptions in spatial memory retrieval caused by acute stress (Wong et al., 2007 PNAS 104:11471). The present experiments were designed to assess whether a similar mechanism is involved in recognition memory. Recognition memory retrieval was assessed in Sprague–Dawley rats using an object recognition test and an object–place recognition test, both of which rely on patterns of spontaneous exploration. Exposure to acute stress for 30 min immediately before the test phase of either test disrupted memory retrieval. Administration of the GluN2B-selective antagonist Ro25-6981 (6 mg/kg; i.p.) enhanced memory in the object recognition test regardless of whether animals were exposed to acute stress. In the object–place test, Ro25-6981 had no effect on memory retrieval in the absence of stress but promoted memory following acute stress. These data highlight the specific contributions made by GluN2B-containing NMDA receptors to recognition memory for different types of stimuli.     

Effects of repetition of mental operations on memory for occurrence and origin

In two experiments, subjects read or generated items at both encoding and retrieval. At test, they were required to decide whether or not the targets were presented initially (recognition), and if so, whether they were initially read or generated (judgments of origin). Recognition for items that were initially generated was enhanced if they were once again generated at test in the same context, but not if they were generated at test without context. These results confirm that memory for occurrence is facilitated by repetition of the initial encoding operations at retrieval. Generating at test resulted in an increase in "generate" responses both for items that were initially generated and for items that were initially read. Overall, there was a decrease in the accuracy of origin discriminations. It is suggested that, when subjects generate at test, they are likely to mistakenly attribute these just-performed operations to be part of the memory trace for that item.     

The impact of post-learning sleep vs. wakefulness on recognition memory for faces with different facial expressions

A beneficial effect of sleep after learning, compared to wakefulness, on memory formation has been shown in many studies using a variety of tasks. However, none of these studies has specifically addressed recognition memory for faces so far. The recognition of familiar faces, together with the extraction of emotional information from facial expression, is a fundamental cognitive skill in human everyday life, for which specific neural systems and mechanisms of processing have been developed. Here, we investigated the role of post-learning sleep for later recognition memory for neutral, happy, and angry faces. Twelve healthy subjects, after judging the emotional valence of the faces in the evening (learning phase), either slept normally in the subsequent night, with sleep recorded polysomnographically (sleep condition), or remained awake (wake condition) according to a cross-over design. Recognition testing took place in the second evening after learning, i.e. after a further night of regular sleep spent at home. Sleep after learning, compared to wakefulness, enhanced memory accuracy in recognition memory. This effect was independent of the emotional valence of facial expression. The response criterion at recognition testing did not differ between sleep and wake conditions. The amount of non rapid eye movement (NonREM) sleep during post-learning sleep correlated positively with memory accuracy at recognition testing, while time in REM sleep was associated with a speeded responding to the learned faces. Results suggest that face recognition, despite its dependence on specialized brain systems, nevertheless relies on the general neural mechanisms of sleep-associated memory consolidation.     

The decay of short-term implicit memory: Unpacking lag

McKone (1995) reported a short-lived repetition priming effect, superimposed on long-lived priming. This short-term implicit memory survived a few intervening items and several seconds for words but decayed precipitously for nonwords, producing a lag 3 lexicality interaction. Here, mechanisms of decay are studied by disconfounding the time delay and interference components of lag. In Experiment 1, time delay was varied while number of intervening items was held constant, and vice versa. In Experiment 2, priming was plotted as a function of time delay, with and without intervening items. Using a lexical decision task, both experiments found independent contributions of time and interference to the decay of short-term priming. Further, Experiment 2 attributed the lag 3 lexicality interaction to a particular sensitivity of nonword traces to interference. An illustration of how these effects might arise in the word recognition system is provided.     

Scent-evoked nostalgia

Declarative and non-declarative memories are thought be supported by two distinct memory systems that are often posited not to interact. However, Wagner, Maril, and Schacter (2000a) reported that at the time priming was assessed, greater behavioural and neural priming was associated with lower levels of subsequent recognition memory, demonstrating an interaction between declarative and non-declarative memory. We examined this finding using a similar paradigm, in which participants made the same or different semantic word judgements following a short or long lag and subsequent memory test. We found a similar overall pattern of results, with greater behavioural priming associated with a decrease in recognition and recall performance. However, neither various within-participant nor various between-participant analyses revealed significant correlations between priming and subsequent memory performance. These data suggest that both lag and task have effects on priming and declarative memory performance, but that they are largely independent and occur in parallel.     

Does the presence of priming hinder subsequent recognition or recall performance?

Declarative and non-declarative memories are thought be supported by two distinct memory systems that are often posited not to interact. However, Wagner, Maril, and Schacter (2000a) reported that at the time priming was assessed, greater behavioural and neural priming was associated with lower levels of subsequent recognition memory, demonstrating an interaction between declarative and non-declarative memory. We examined this finding using a similar paradigm, in which participants made the same or different semantic word judgements following a short or long lag and subsequent memory test. We found a similar overall pattern of results, with greater behavioural priming associated with a decrease in recognition and recall performance. However, neither various within-participant nor various between-participant analyses revealed significant correlations between priming and subsequent memory performance. These data suggest that both lag and task have effects on priming and declarative memory performance, but that they are largely independent and occur in parallel.     

Repetition effects in associative false recognition: Theme-based criterion shifts are the exception, not the rule

Previous reports have demonstrated that false memory for the critical items of associative lists decreases when lists are studied multiple times (Benjamin, 2001). In three experiments, we explored two hypotheses that might account for false memory reductions with repetition. Under an identification hypothesis, repetition decreases false memory because participants realise that critical items are absent from the list at encoding and thus reject them at test. Under a criterion shift hypothesis, repetition decreases false memory because it increases the discriminability of studied words from lures, causing participants to set a higher response criterion for positive recognition responses. Results uniquely supported the criterion shift hypothesis. Furthermore, results showed that participants only changed their criterion on separate recognition tests, not on an item-by-item basis within a single recognition test. The failure to establish separate criteria within a test increased false memory for repeated lists.     

Recognition memory strength is predicted by pupillary responses at encoding while fixation patterns distinguish recollection from familiarity

Thirty-five healthy participants incidentally encoded a set of man-made and natural object pictures, while their pupil response and eye movements were recorded. At retrieval, studied and new stimuli were rated as novel, familiar (strong, moderate, or weak), or recollected. We found that both pupil response and fixation patterns at encoding predict later recognition memory strength. The extent of pupillary response accompanying incidental encoding was found to be predictive of subsequent memory. In addition, the number of fixations was also predictive of later recognition memory strength, suggesting that the accumulation of greater visual detail, even for single objects, is critical for the creation of a strong memory. Moreover, fixation patterns at encoding distinguished between recollection and familiarity at retrieval, with more dispersed fixations predicting familiarity and more clustered fixations predicting recollection. These data reveal close links between the autonomic control of pupil responses and eye movement patterns on the one hand and memory encoding on the other. Moreover, the data illustrate quantitative as well as qualitative differences in the incidental visual processing of stimuli, which are differentially predictive of the strength and the kind of memory experienced at recognition.     

Recognition memory strength is predicted by pupillary responses at encoding while fixation patterns distinguish recollection from familiarity

Thirty-five healthy participants incidentally encoded a set of man-made and natural object pictures, while their pupil response and eye movements were recorded. At retrieval, studied and new stimuli were rated as novel, familiar (strong, moderate, or weak), or recollected. We found that both pupil response and fixation patterns at encoding predict later recognition memory strength. The extent of pupillary response accompanying incidental encoding was found to be predictive of subsequent memory. In addition, the number of fixations was also predictive of later recognition memory strength, suggesting that the accumulation of greater visual detail, even for single objects, is critical for the creation of a strong memory. Moreover, fixation patterns at encoding distinguished between recollection and familiarity at retrieval, with more dispersed fixations predicting familiarity and more clustered fixations predicting recollection. These data reveal close links between the autonomic control of pupil responses and eye movement patterns on the one hand and memory encoding on the other. Moreover, the data illustrate quantitative as well as qualitative differences in the incidental visual processing of stimuli, which are differentially predictive of the strength and the kind of memory experienced at recognition.     

Components of visual memory

Visual recognition memory for a sequence of non-verbalized patterns is shown to have a large and clearly defined recency effect. This recency effect occurs with random list lengths and therefore cannot be due to differential processing of the end items. The effect is completely removed by just 3 s of mental arithmetic but survives for at least 10 s over unfilled intervals. Recognition memory for patterns at other serial positions is slower, less accurate, and shows no primacy effect; performance at these earlier serial positions is dependent upon the time for which patterns are initially presented, but is unaffected by the duration of the retention interval, mental arithmetic, and the time between patterns on initial presentation. These findings provide evidence that visual memory has two components that are closely analogous to the short-term (STM) and long-term (LTM) components of verbal memory. Visual STM, here called visualization, has a capacity of one pattern, cannot be activated LTM, and does not seem to be the gateway to LTM.     

The mapping from sound structure to the lexicon in aphasia: evidence from rhyme and repetition priming

Two studies were conducted to explore the hypothesis that Broca's and Wernicke's aphasics have deficits arising from the processes involved in activating the lexicon from phonological form. The first study explored whether phonologically similar lexical entries differing only in their initial consonants show "rhyme priming." Results revealed that Broca's aphasics failed to show facilitation when the target was identical to the prime (i.e. identity priming) and they showed significant inhibition when targets were preceded by rhyming words. Wernicke's aphasics showed a pattern of results similar to that of normal subjects, i.e., identity priming and rhyme priming as well as significantly slower reaction-times in the rhyming condition compared to the identity condition. The second study investigated form-based repetition priming in aphasic patients at a number of intervals including when no other stimuli intervened between repeated stimuli (0 lag) or when 4, 8, or 12 stimuli intervened. Results showed that, unlike old normal subjects who showed repetition priming for both words and nonwords, both Broca's and Wernicke's aphasics showed repetition priming for word targets only. Moreover, in contrast to old normal subjects who showed a greater magnitude of priming at 0 lag for word targets, neither Broca's aphasics or Wernicke's aphasics showed priming at 0 lag. Implications of these findings are considered with respect to the hypotheses that Broca's and Wernicke's aphasics have deficits in the nature of the activation patterns within the lexicon itself and in auditory (working) memory.     

Exploring the memory advantage for moving scenes

Recognition memory is better for moving images than for static images (the dynamic superiority effect), and performance is best when the mode of presentation at test matches that at study (the study–test congruence effect). We investigated the basis for these effects. In Experiment 1, dividing attention during encoding reduced overall performance but had little effect on the dynamic superiority or study–test congruence effects. In addition, these effects were not limited to scenes depicting faces. In Experiment 2, movement improved both old–new recognition and scene orientation judgements. In Experiment 3, movement improved the recognition of studied scenes but also increased the spurious recognition of novel scenes depicting the same people as studied scenes, suggesting that movement increases the identification of individual objects or actors without necessarily improving the retrieval of associated information. We discuss the theoretical implications of these results and highlight directions for future investigation.     

重复学习对错误记忆通道效应的影响

本研究采用DRM范式以80名大学生为被试对错误记忆的通道效应进行了研究.实验采用三因素混合设计,运用信号检测论等方法探讨了重复学习对不同通道错误再认的影响.结果发现:1)汉语词表具有与英文词表不同的通道效应,表现为视觉学习的错误再认高于听觉学习;2)重复学习对视觉学习与听觉学习的错误再认产生分离性影响,即重复学习降低了视觉学习的错误再认,却提高了听觉学习的错误再认;3)信号检测论的分析表明:听觉学习在重复学习后对关键诱词的错误再认的增加是听觉学习对要义信息日益增加的敏感性连同较为宽松的提取标准协同起作用的结果.