Developmental and individual differences in visual memory span

The effects of chronological age (5+, 7+, 10+, and adult), articulatory suppression and spatial ability were assessed on three measures (recognition memory, partial recall, and free recall) of visual memory span for patterns, using a procedure devised by Wilson, Scott & Power (1987). Although span increased into adulthood for all three tasks, concurrent articulatory suppression acted to reduce span for the 10-year-old and adult subjects. The ability to generate accurate visuo-spatial representations at retrieval is perfectly well developed by 7 years of age. Speed of response was lengthened for the youngest age group, but was immune to the effects of concurrent articulatory suppression. Good spatial ability was associated with higher span estimates on all tasks, regardless of age. Whilst the data support the existence of a system for representing visual patterns, which increases in capacity with increasing chronological age, the system (or processes accessing it at retrieval) is not immune to verbal recoding strategies. The independent association of spatial ability with span is taken to imply that nonverbal encoding and/or maintenance strategies can act to boost visual span from at least 5 years of age.     

Working memory recall precision is a more sensitive index than span

Delayed adjustment tasks have recently been developed to examine working memory (WM) precision, that is, the resolution with which items maintained in memory are recalled. However, despite their emerging use in experimental studies of healthy people, evaluation of patient populations is sparse. We first investigated the validity of adjustment tasks, comparing precision with classical span measures of memory across the lifespan in 114 people. Second, we asked whether precision measures can potentially provide a more sensitive measure of WM than traditional span measures. Specifically, we tested this hypothesis examining WM in a group with early, untreated Parkinson's disease (PD) and its modulation by subsequent treatment on dopaminergic medication. Span measures correlated with precision across the lifespan: in children, young, and elderly participants. However, they failed to detect changes in WM in PD patients, either pre‐ or post‐treatment initiation. By contrast, recall precision was sensitive enough to pick up such changes. PD patients pre‐medication were significantly impaired compared to controls, but improved significantly after 3 months of being established on dopaminergic medication. These findings suggest that precision methods might provide a sensitive means to investigate WM and its modulation by interventions in clinical populations.     

Effects of generation on immediate memory span and delayed unexpected free recall

We investigated the effects of generating words from fragments on pronunciation time, on immediate memory span, and on delayed free recall. Subjects read long words and short words aloud or generated them from strings with missing letters. Word-length and generation condition had multiplicative effects on speaking rate, as expected if each affected a separate process regulating the rate. We replicated the standard finding that span is smaller for longer words. Generation improved delayed free recall, indicating that relatively brief presentation times are adequate to produce a generation effect. Although generation improved long-term memory for the words, memory span was shorter for the words that were generated. The harmful effect of generation on span appears to be due to its slowing of speaking rate.     

Verbal and visual recall span curves between 1 ms and 1 min

Summary The recall spans for verbal and visual information were represented, respectively, in terms of the number of digits and the number of dots in a 5×5 matrix. They were measured independently by the method of limits as functions of presentation times which ranged from 1 ms to 64 s. The curves were very similar: each had two plateaus, one at 10 to 100 ms and one at 2 to 8 s presentation levels. These plateaus suggest two kinds of capacity limitation on information processing. The first limitation is concerned with the transfer of information from iconic memory to short-term memory (STM); the second indicates the saturation of the limited capacity short-term store. Short-term and long-term mechanisms are involved not only in verbal memory but also in visual memory, since the second plateau followed by an increasing portion appears in the visual span curve as well as in the verbal one. Finally, the distinction between verbal and visual STM is discussed, based on a) the selective interference effects of distracting tasks upon the retention of verbal and visual materials, and b) the weak correlation between verbal and visual spans.     

The effect of mood-context on visual recognition and recall memory

Although it is widely known that memory is enhanced when encoding and retrieval occur in the same state, the impact of elevated stress/arousal is less understood. This study explores mood-dependent memory's effects on visual recognition and recall of material memorized either in a neutral mood or under higher stress/arousal levels. Participants' (N = 60) recognition and recall were assessed while they experienced either the same o a mismatched mood at retrieval. The results suggested that both visual recognition and recall memory were higher when participants experienced the same mood at encoding and retrieval compared with those who experienced a mismatch in mood context between encoding and retrieval. These findings offer support for a mood dependency effect on both the recognition and recall of visual information.     

Implicit and explicit memory for visual patterns

The article reports an investigation of implicit and explicit memory for novel, visual patterns. Implicit memory was assessed by a speeded perception task, and explicit memory by a four-alternative, forced-choice recognition task. Tests were given either immediately after testing or 7 days later. The results suggest that a single exposure of a novel, nonverbal stimulus is sufficient to establish a representation in memory that is capable of supporting long-lived perceptual priming. In contrast, recognition memory showed significant loss over the same delay. Performance measures in the two tasks showed stochastic independence on the first trial after a single exposure to each pattern. Finally, a specific occurrence of a previously studied item could be retrieved from explicit memory but did not affect the accuracy of perception in the implicit memory test. The results extend the domain of experimental dissociations between explicit and implicit memory to include novel, nonverbal stimuli.     

Perfect visual short-term memory for periodic patterns

Abstract

The short-term memory for spatial frequency information was assessed by measuring the spatial frequency discrimination thresholds for briefly flashed luminance gratings as a function of the time interval between the test and reference gratings, using a computer-controlled two-interval forced-choice procedure. Discrimination thresholds were stable for interstimulus intervals in the range 1–30 sec under all conditions tested. At low contrasts, short exposure times and low spatial frequencies discrimination thresholds increased, but no interactions between stimulus parameters affecting thresholds and interstimulus interval were observed. It is concluded that factors limiting spatial discrimination are associated with the sensory coding stage. Spatial discrimination and visual memory may be based on a common representation, which is perfectly retained in short-term memory. Visual half-field tests revealed no hemispheric differences in the processing and retention of spatial frequency information.     

Response-contingent variation in visual recall: evidence of a dynamic memory trace

Sixty-six subjects learned responses to four ellipses (eccentrically 0.52) which varied orthogonally in area (two large: 994 mm2; two small: 671 mm2) and orientation (two with major axis vertical, two with major axis horizontal). Correct responses were contingent on either the area or the orientation of the ellipses. After learning the correct responses, subjects recalled the ellipses by drawing them. Recall was either immediately, 1 day, or 2 weeks after learning the responses. The recall drawings were measured for area and for orientation (ratio of the length of the vertical to the horizontal axis). Differences among the recall drawings increased on the dimension (area or orientation) which was associated with correct responses during the learning task. The differences on the associated dimension were large when recall was tested immediately after the response learning task, small when recall was tested 1 day after learning, and large again when recall was tested 2 weeks after learning the responses. This experiment eliminated one potential source of uncontrolled variability in earlier results. The results are consistent with previous experiments and suggest an active two-phase memory consolidation process extended over time.     

Trees as memory representations for simple visual patterns

The form of the memory representation for visual patterns consisting of a few line segments was investigated with three tasks. One task was the reproduction of remembered patterns using pencil and paper. The order in which the subparts of those patterns were reproduced was used to make suggestions about possible memory representations for the patterns. The second task involved rating the “goodness” of subparts of the patterns. These ratings were also interpreted as reflecting the underlying representations of the patterns. In the third task, the time required to recognize that a small pattern was part of a larger remembered pattern was used as further evidence about the memory representations of the patterns. The results from all three tasks are consistent with the theory that the memory representations are tree structures. Methods for deriving and comparing tree structures are discussed.     

Impaired visual and odor recognition memory span in patients with hippocampal lesions

In a recent study, rats with hippocampal lesions performed as well as did unoperated rats on an olfactory memory span task, performing ~80% correct even when the span length reached 24 odors. This finding seems potentially at odds with demonstrations that memory-impaired patients typically fail tasks in which large amounts of information must be retained. Accordingly, we have assessed recognition memory span performance for line drawings of objects, designs, and odors in amnesic patients with damage thought to be limited to the hippocampal region. The patients were impaired on all three tasks. We consider possible explanations for the difference between the findings for humans and rats, including the fact that olfactory function is particularly well-developed in rodents.     

Validating running memory span: Measurement of working memory capacity and links with fluid intelligence

We manipulated running memory span tasks to examine effects on recall and relations with criterion measures of working memory capacity and general fluid intelligence. The goal of the manipulations was to limit or enhance opportunities for active input processing and response preparation in advance of test. We manipulated presentation rate in Experiment 1. Recall was higher at slow than at fast rates, but correlations with criterion measures were much the same across rate conditions. In Experiment 2, we manipulated the time at which the number of items to report was made known to the participants. They were given that information in advance (precue) or at test (postcue). Recall scores and correlations with criterion measures were much the same across cuing conditions. We conclude that running memory span provides valid measurement of working memory capacity that is predictive of higher order cognition across a wide range of conditions.     

Cognitive categories and memory span: II. The effect of temporal vs. categorical recall

Subjects were presented with mixed lists of elements chosen from at least two formally distinct cognitive categories and were instructed to recall either temporally (i.e. in the actual order of arrival), or categorically (i.e. first all elements of one category followed by those of the other). Temporal recall is found to be superior when the categories are even and uneven digits; categorical recall is better when consonants and tones or consonants and spatial positions are mixed. Approximately equal performance is found with consonants and digits. It is suggested that efficiency of recall strategy depends on the relative strength of pre-existing associative bonds between elements from different cognitive categories. When these connections are weaker the probability increases that class membership rather than succession in time determines the assimilation of the list. It is found that with consonants and digits it does not matter whether instruction is given before or after presentation. This suggests that both recall modes can be activated at the same time. The implication of this result for work on dichotic listening is discussed.     

Information and the memory span

Messages differing in number of symbols and symbol information load were presented tachistoscopically to 4 adult Ss, The messages were constructed by random drawing with replacement from an alphabet of 8 black form symbols and an alphabet of 32 colored form symbols. The number of symbols recalled varied as a function of alphabet; however, the information in recall was constant for all conditions. The number of symbols recalled and the information in recall was independent of message length.     

Information and the memory span

Messages differing in number of symbols and symbol information load were presented tachistoscopically to 4 adult Ss. The messages were constructed by random drawing with replacement from an alphabet of 8 black form symbols and an alphabet of 32 colored form symbols. The number of symbols recalled varied as a function of alphabet; however, the information in recall was constant for all conditions. The number of symbols recalled and the information in recall was independent of message length.     

Grouping and short-term memory: Different means and patterns of grouping

Two experiments, concerned with the improving effects of grouping on auditory short-term memory, are described. In the first, temporal grouping was found to improve recall considerably, but non-temporal grouping had a much smaller effect. Temporal grouping reduced the order errors more than other errors; it also changed the pattern of the order errors. Further, it altered the shape of the serial position curve of all errors. In the second experiment, irregular patterns of temporal grouping were found to be inferior to a regular pattern. The results are discussed in terms of the time available for processing previous items during the presentation of a sequence, and the form that this processing may take.     

The intricacy of memory span

The effects of word frequency on memory span were explored using the “up-and-down” method. Mean spans were greatest when the sequences were of all high-frequency words (5.82), and smallest when they were of all low-frequency words (4.24). For mixed-frequency sequences, mean spans were greater when the high-frequency words were presented before the low-frequency words (5.19) than when the low-frequency words came first (4.65). The findings are discussed in terms of the primary-secondary memory distinction worked out for single-trial free recall, and the logic of this distinction is used to argue against attributing span performance to a simple unitary process.