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.     

Using immediate memory span

To avoid some conceptual and methodological pitfalls found in traditional artificial grammar learning tasks, we developed a new method of measuring implicit learning using immediate memory span. Subjects were presented with sequences generated by an artificial grammar and were asked to reproduce the patterns by pressing buttons on a response box. After exposure to these sequences, subjects showed selective improvement in immediate memory span for novel sequences governed by the same grammar. Individual differences in implicit learning covaried with measures of auditory digit span. Subjects with greater immediate memory processing capacity were better able to learn and subsequently exploit the information available in grammatical sequences. Our results are consistent with a detailed episodic coding framework in which implicit learning occurs as an incidental by-product of explicit task performance. Although subjects encode highly detailed information about specific instances, they use different aspects of this information to accomplish different task-specific demands.     

Silent reading rate and memory span

This paper reports two experiments concerned with the form of the linear function relating memory span to pronunciation rate. Experiment 1 asked whether the intercept of the equation is attributable to an interaction between modality, word‐length, and serial position. The results lead us to reject this possibility. Experiment 2 examined the shape of the span function for visual presentation of lists read aloud or silently. The results show that the intercept of the span function disappears for silent presentation but not for aloud presentation. The results are discussed in terms of a balance between two opposing effects of word‐length.     

Silent reading rate and memory span

This paper reports two experiments concerned with the form of the linear function relating memory span to pronunciation rate. Experiment 1 asked whether the intercept of the equation is attributable to an interaction between modality, word-length, and serial position. The results lead us to reject this possibility. Experiment 2 examined the shape of the span function for visual presentation of lists read aloud or silently. The results show that the intercept of the span function disappears for silent presentation but not for aloud presentation. The results are discussed in terms of a balance between two opposing effects of word-length.     

Age differences in memory span

Five-year-olds recalled fewer items than adults in memory-span tasks involving both familiar and unfamiliar faces. This occurred even though the use of rehearsal and recoding strategies was minimized for adults. This residual age difference may be partially accounted for by two further processing limitations in children. The five-year-olds needed more time than adults to name a face (Experiment 1) and to encode a face (Experiment 2). In order to test whether limitations in children's initial recognition and stimulus-identification processes could account for recall performance, Experiment 3 reduced adults' exposure duration in the memory-span task. This led to a drastic reduction in the age difference. Other factors contributing to remaining age differences included adults' adaptability in using various alternative encoding and retrieval strategies which elevated their recall performance.     

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.     

Processing and storage in working memory span

Two experiments are reported that address theoretical assumptions as to the nature of working memory involved in working memory span tasks (Daneman & Carpenter, 1980). Experiment 1 used a version of the sentence span task, and Experiment 2 combined arithmetic verification with recall of presented words. In each experiment, working memory processing span was assessed independently of temporary storage span prior to their combination. Combined task performance under high demand for each component resulted in substantial residual performance for both task elements, particularly in Experiment 2. The results do not challenge the utility of the sentence span task as a measure of on-line cognition, but they raise concerns as to how resource might be allocated to processing and storage elements of the task within a single flexible resource pool, or between different resources of a multiple component working memory system. Although both models lack predictive power regarding resource allocation in these tasks, the multiple resource model appears to offer the better account.     

Operational efficiency and the growth of short-term memory span

Four studies are reported which link developmental increases in memory span with developmental increases in operational speed or efficiency. In the first, a linear relationship is demonstrated between increases in word span and increases in speed of word repetition. In the second, adults and 6-year-olds are equated on speed of word repetition, by manipulating word familiarity. It is shown that their word spans are no longer different under these conditions. Similar findings are then reported for a test of M space called “Counting Span.” First, a linear relationship is demonstrated between increases in Counting Span and increases in speed of counting. Next, adults and 6-year-olds are equated on speed of counting, by forcing adults to count in an unfamiliar language. It is shown that their counting spans are no longer different under these conditions. The conclusion is that developmental increases in memory span do not result from increases in total processing space. Rather, with development, basic operations become faster and more efficient. This means that they require less processing space, and that more space becomes available for storage as a result.     

Speech rate and the development of short-term memory span

Two experiments are reported which examine the effects of word duration on memory span in subjects of different ages. The same linear function relating recall to speech rate (assessed by the speed of repeating words) fits the results of subjects ranging in age from 4 years old to adulthood. It is concluded that developmental increases in short-term memory span can be explained in terms of increases in speech rate and that there is no evidence for an increase in short-term memory capacity. Analyses of the children's speech suggests that increases in speech rate with age reflect increases in the speed of articulation of individual words, rather than any change in the duration of pauses between successive words or changes in coarticulation between words.     

Further evidence of the intricacy of memory span

Memory span was measured for lists of verbal items constructed such that the items in the first half of the list were of one category and those of the second half were of another. In Experiment 1, the lists consisted of digits and words (e.g., 2, 8, 7, horse, cow, sheep or horse, cow, sheep, 2, 8, 7); in Experiment 2, they consisted of words from the same semantic domain and words from different semantic domains; in Experiments 3 and 4, they consisted of words that rhymed and words that did not rhyme. A category-order effect occurred in each experiment: Span was larger when the digits, same-domain words, or rhyming words occurred in the first half of the list than when they occurred in the second half. These findings suggest that memory span is more complex than is generally assumed.     

Strategic grouping in the spatial span memory task

Spatial short-term memory performance was examined in relation to participants' strategies. A total of 20 adult participants viewed and reproduced sequences of locations that varied in length (five, six, seven, or eight locations) and spatial separability (a manipulation of the configurations). In trial-by-trial self-reports, participants described five types of strategies. Chunking the spatial sequences into groups of three or four locations was the sole strategy associated with increased accuracy. Participants demonstrated considerable variability in the strategies that they selected, suggesting that cognitive resources are allocated to strategy selection, execution, and monitoring in the spatial span task. Spatially separable sequences were more accurately recalled than nonseparable sequences, independent of strategic grouping, suggesting two levels of grouping in the spatial span task.     

Working memory span and the role of proactive interference.

The authors investigated the possibility that working memory span tasks are influenced by interference and that interference contributes to the correlation between span and other measures. Younger and older adults received the span task either in the standard format or one designed to reduce the impact of interference with no impact on capacity demands. Participants then read and recalled a short prose passage. Reducing the amount of interference in the span task raised span scores, replicating previous results (C. P. May, L. Hasher, & M. J. Kane, 1999). The same interference-reducing manipulations that raised span substantially altered the relation between span and prose recall. These results suggest that span is influenced by interference, that age differences in span may be due to differences in the ability to overcome interference rather than to differences in capacity, and that interference plays an important role in the relation between span and other tasks.     

Cytokines and memory across the mature life span of women

Increasing evidence suggests a role of the immune system in modulation of cognition, but details on affected memory systems are largely lacking. We therefore aimed to study the relation between selected cytokines and subsets of memory, and the impact of age in these relations. From a random population-based sample (the Betula Prospective Cohort Study), 298 women (age 45-90) were studied in terms of episodic recall and recognition, semantic fluency and knowledge, and prospective memory. Circulating cytokines of relevance for cognition and aging were measured with ELISA. Levels of interleukin (IL)-6 and sIL-2R were significantly and negatively associated with most cognitive variables, while the opposite was true for IL-1β. Age shared substantial variance with both cytokines and memory, and turned most correlations non-significant when controlled for together with education, BMI and presence of disease. Interactions between age and cytokines were further analyzed in multiple regressions. For IL-6, significant negative interactions with age were found for semantic fluency (p<0.05) and prospective memory (p<0.01), and for sIL-2R in predicting semantic knowledge (p<0.05), indicating an increased negative impact of these cytokines on memory with increasing age. In conclusion, the study indicates a relation between cytokines and memory that appears to be largely mediated by age, and supports the suggestion that cytokine dysregulation with higher age may interact with cognitive aging.     

Word frequency,articulatory suppression and memory span

Watkins (1977) found memory span was longer when first and second halves of lists contained high- and low-frequency words, respectively, than when low-frequency words preceded high. One of the four experiments reported here failed to replicate this finding and found that articulatory suppression had a greater detrimental effect on span for high- than for low-frequency words. Another experiment showed that high-frequency words similar to those used by Watkins were easier to articulate than low-frequency words. In the third experiment articulatory suppression did not differentially affect delayed recall of high- and low-frequency words. The fourth experiment showed span for high- and low-frequency words was influenced in a similar way when encouraging subjects to maintain words from either early or late serial positions by articulatory rehearsal. It is concluded that differences in the strategies adopted to maintain words in the articulatory rehearsal loop can account for inconsistencies in the results obtained here and in previous experiments.     

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.     

Mapping the developmental constraints on working memory span performance

This study investigated the constraints underlying developmental improvements in complex working memory span performance among 120 children of between 6 and 10 years of age. Independent measures of processing efficiency, storage capacity, rehearsal speed, and basic speed of processing were assessed to determine their contribution to age-related variance in complex span. Results showed that developmental improvements in complex span were driven by 2 age-related but separable factors: 1 associated with general speed of processing and 1 associated with storage ability. In addition, there was an age-related contribution shared between working memory, processing speed, and storage ability that was important for higher level cognition. These results pose a challenge for models of complex span performance that emphasize the importance of processing speed alone.     

Working memory span: the effect of prior learning

Recent work suggests that working memory span (WMS) tasks are not simple measures of the capacity to simultaneously store and process new information. Instead, these measures may be influenced by numerous factors, including proactive interference (PI). The current study examined whether WMS, like other memory tasks, is also influenced by PI from prior memory experiments. Experimentally experienced and naive participants completed a speaking span task. Span scores were lower for experienced than for naive participants, but other cognitive scores were not. In combination with other work, these results suggest that WMS estimates are not pure measures of capacity and may be partially determined by PI.