Short-term memory for flavour

The short-term memory for the flavour of a wine in frequent but nonexpert drinkers was studied in an experiment comparing memory for wine under conditions where participants imagined and remembered a target wine with memory under conditions where participants carried out subsequent imaging and image rating tasks on the wine and on competing mental images. The results show that the cognitive operation of mental image rating produced enhanced memory when the operations were performed on the image of the target wine and somewhat impaired memory when operations were performed on an image of a competing flavour or operations performed on mental images in other domains. It is concluded that sensory traces of flavour may be effectively maintained in short-term memory when supported by appropriate encoding operations.     

Short-term memory in autism spectrum disorder

Three experiments examined verbal short-term memory in comparison and autism spectrum disorder (ASD) participants. Experiment 1 involved forward and backward digit recall. Experiment 2 used a standard immediate serial recall task where, contrary to the digit-span task, items (words) were not repeated from list to list. Hence, this task called more heavily on item memory. Experiment 3 tested short-term order memory with an order recognition test: Each word list was repeated with or without the position of 2 adjacent items swapped. The ASD group showed poorer performance in all 3 experiments. Experiments 1 and 2 showed that group differences were due to memory for the order of the items, not to memory for the items themselves. Confirming these findings, the results of Experiment 3 showed that the ASD group had more difficulty detecting a change in the temporal sequence of the items.     

Short-term memory in the pigeon: relative recency

Three pigeons pecked for food in an experiment in which each trial consisted of two phases. The first phase consisted of a pattern of three successively illuminated, randomly selected left or right keys. A subject was required to peck each of the lighted keys as they appeared. Thus, in the first phase, a subject emitted a pattern of three left- or right-key pecks. Over trials, all eight possible patterns appeared. A time interval separated the first phase from the second phase, which began with presentation of a randomly selected one of three cues. A reinforcer was delivered in the second phase if a subject pecked the side key that had appeared in the first phase in an ordinal position corresponding to the cue presented in the second phase. That is, the three cues probed a pigeon's memory for the side key it had pecked first, second, or third, in the first phase of a trial. The results show that a pigeon can remember for more than 4 sec the order in which it has just seen and pecked two lighted keys: a pigeon can remember the temporal organization or pattern of events in its recent environment. Consequently, the functional stimulus present when a reinforcer is delivered may include a subject's short-term memory for the temporal organization of recent events, such as the pattern of its own recent behavior. This possibility is consistent with a molecular analysis of operant behavior focusing on local patterns of behavior.     

Short-term memory function in young readers

Twelve good readers and 12 poor readers, 10-y4-olds, were given memory span tests, and memory scanning tests, in both auditory and visual modalities. Their concept of a letter pattern was also tested. The major finding was that short-term memory (STM) function deteriorated over time in the poor reading group. When modality was switched the good readers showed a release from proactive inhibition (PI); the poor readers did not. Among good readers, memory scanning in the auditory modality occurred at about the same speed as memory scanning in the visual modality; among the poor readers, auditory speed gradually lagged relative to visual rates. Poor readers were more likely (than good readers) to lack the concept of a letter pattern. Stepwise regressions showed that different patterns of variables were assocated with different types of reading errors. Implicatios for model construction were discussed.     

Short-term memory in the pigeon: stimulus-response associations

Three pigeons pecked for food in two experiments in which each trial consisted of two phases: a study and a test phase. The study phase in Experiment I consisted of two stimulus-response pairs presented successively. Each pair consisted of the illumination of a left or right key (the stimulus) and a peck on the lighted side key (the response). The study phase in Experiment II consisted of three such pairs presented successively. A retention interval, varied between 0.1 and 4.0 sec, separated the study phase from the test phase. The test phase of a trial began with the illumination of the center key by one of two (Experiment I) or three (Experiment II) colors. This color was the same as the stimulus element of one of the pairs in the study phase. A reinforcer was presented if a subject then emitted the response element of the indicated stimulus-response pair. The results provide information on the conditions that enable a pigeon to remember the responses most recently emitted in the presence of various stimuli. The results suggest an account of the maintenance of behavior that is temporally noncontiguous with reinforcement.     

Short-term memory for intonation.

Ss were presented with lists of 16 words, each word spoken in one of four intonations. The final word was a repetition of one of the first 15 words, 40 Ss having to judge whether it was spoken in the same intonation as its earlier occurrence. A control group of 40 Ss did a similar task, ignoring intonation. Retention of intonation was significantly poorer, indicating that intonation is an additional load not normally retained. This argues against acoustic or articulatory encoding in short-term memory and in favor of an abstract-verbal encoding mode. Results are also interpreted as supporting the position that verbal and motor short-term membory obey similar laws.     

Short-term memory and aphasia.

Short-term retention tests of verbal item information (short-term memory for items) and order information (memory for sequences) were administered to aphasic, nonaphasic brain-damaged, and normal subjects. Memory for both parameters was significantly impaired in aphasics only. One-third of errors made by aphasics resulted from a specific, separable defect in short-term memory for sequences. As information load increased, memory for sequences became critical for linguistic performance of aphasics.     

Short-term recognition memory of tones

Four Os participated in a recognition memory experiment for a period of 5 weeks. The task required O to judge whether two temporally sequenced tones (ISI = 0.5, 2.0, or 8.0 sec) were the “same” or “different ” Latencies and confidence ratings were obtained for each judgment. TSD analyses applied to individual O’s data indicated consistent and rapidly decreasing d’s as a function of ISI. ROC functions generated from the latencies and ratings produced comparable results, indicating the feasibility of using latency measures along with the type of judgments made to obtain sensitivity measures. Response bias, as indicated by the differences in the latencies between “same” and “different” judgments, did not produce consistent trends.     

Short-term memory for time intervals

The effect of intertrial interval, preset interval, and retention interval on the performance of rats in a time estimation task was described. On each trial a signal was presented for a duration of 2 to 8 sec. Eighteen rats were trained to press one lever (the short response) if the signal was shorter than 4 sec, and another lever (the long response) if the signal was longer than 4 sec. When trials were massed (Experiment 1), the percentage long response was affected by the classification of the previous signal, but not by its actual duration. This suggests that the animals remembered the response made on the previous trial, but not the signal duration. If a response was not permitted on the previous trial (Experiment 2), the duration or classification of the previous signal had no effect on performance. This supports the conclusion from the first experiment and suggests that an animal can reset its internal clock in less than 2 sec. In Experiment 3, the difference limen of the psychophysical function increased with the duration of the retention interval, but the point of subjective equality did not change. This suggests that resetting of the internal clock occurs on a non-time dimension.     

Short-term memory performance in the absence of phonological coding

These experiments examined the short-term memory performance of an aphasic patient with posterior damage who shows a selective deficit in phonological coding. In recognition memory tests, the patient relied on both visual and semantic coding, and often showed an essentially normal level of accuracy. However, for memory sets consisting of four function words, his performance was quite impaired. Also, his retention of order information was far below that of normal controls. The implications of these deficits in short-term memory for language comprehension and production are discussed.     

Short-term memory and information processing in pigeons

Six pigeons were trained to asymptotic performance on a variable-delay matching-to-sample task in which the samples were sometimes line or color elements and sometimes line-color compounds. On compound-sample trials, the comparison stimuli were sometimes color elements and sometimes line-tilts. Sample type and delay (0, 1.5, and 4.5 sec) were varied within sessions, and sample duration (.4, 1.0, and 3.0 sec) was varied between sessions. Forgetting curves were steeper for line-tilt than for color. As sample duration increased, matching performance improved more for colors than for line-tilts, especially at delays greater than zero. Performance was better with element samples than with compound samples only on the line-tilt dimension at zero delay. Some predictions of a unitary trace growth and decay theory of pigeon short-term memory were not confirmed. A dual-code hypothesis was proposed to account for the data.     

Short-term memory for emotional faces in dysphoria

The study aimed to determine if the memory bias for negative faces previously demonstrated in depression and dysphoria generalises from long- to short-term memory. A total of 29 dysphoric (DP) and 22 non-dysphoric (ND) participants were presented with a series of faces and asked to identify the emotion portrayed (happiness, sadness, anger, or neutral affect). Following a delay, four faces were presented (the original plus three distractors) and participants were asked to identify the target face. Half of the trials assessed memory for facial emotion, and the remaining trials examined memory for facial identity. At encoding, no group differences were apparent. At memory testing, relative to ND participants, DP participants exhibited impaired memory for all types of facial emotion and for facial identity when the faces featured happiness, anger, or neutral affect, but not sadness. DP participants exhibited impaired identity memory for happy faces relative to angry, sad, and neutral, whereas ND participants exhibited enhanced facial identity memory when faces were angry. In general, memory for faces was not related to performance at encoding. However, in DP participants only, memory for sad faces was related to sadness recognition at encoding. The results suggest that the negative memory bias for faces in dysphoria does not generalise from long- to short-term memory.     

Short-term memory in the pigeon: the previously reinforced response

Eighteen pigeons served in a discrete-trials short-term memory experiment in which the reinforcement probability for a peck on one of two keys depended on the response reinforced on the previous trial: either the probability of reinforcement on a trial was 0.8 for the same response reinforced on the previous trial and was 0.2 for the other response (Group A), or, it was 0 or 0.2 for the same response and 1.0 or 0.8 for the other response (Group B). A correction procedure ensured that over all trials reinforcement was distributed equally across the left and right keys. The optimal strategy was either a winstay, lose-shift strategy (Group A) or a win-shift, lose-stay strategy (Group B). The retention interval, that is the intertrial interval, was varied. The average probability of choosing the optimal alternative reinforced 80% of the time was 0.96, 0.84, and 0.74 after delays of 2.5, 4.0, and 6.0 sec, respectively for Group A, and was 0.87, 0.81, and 0.55 after delays of 2.5, 4.0, and 6.0 sec, respectively, for Group B. This outcome is consistent with the view that behavior approximated the optimal response strategy but only to an extent permitted by a subject's short-term memory for the cue correlated with reinforcement, that is, its own most-recently reinforced response. More generally, this result is consistent with “molecular” analyses of operant behavior, but is inconsistent with traditional “molar” analyses holding that fundamental controlling relations may be discovered by routinely averaging over different local reinforcement contingencies. In the present experiment, the molar results were byproducts of local reinforcement contingencies involving an organism's own recent behavior.     

Short-term haptic memory for three-dimensional objects

In 8 experiments college students felt 32 geometric objects and were tested in a signal-detection framework to same or distractor items. Retention intervals and intervening experiences were also manipulated following initial touching. In all instances performance was high, and there was no evidence of a decline in haptic sensitivity over the retention intervals employed. These surprising results were interpreted as consistent with the 1985 contention of Klatzky, Lederman, and Metzger that the haptic modality constitutes an expert system.     

Short-term memory: A brief commentary

Over the years, a metatheoretical view of short-term memory has developed. This view, closely related to the “modal” model from the 1960s, is supported by an increasing base of neurophysiological data, and a wide variety of empirical findings. It treats short-term memory as (1) the temporary, above threshold, activation of neural structures (related in not-too-well-specified ways to various recency effects); (2) a work space for carrying out virtually all cognitive operations involved in human cognition; and (3) the source of capacity limitations, accounting for certain memory limitations and most attentional limitations. The main problem with this view is the fact that it encompasses virtually everything that we are concerned with in human cognition—asuccessful model would almost be a general model of cognition, something the field has not yet approached. This situation is not grounds for despair. Progress is being made on many fronts, notwithstanding the fact that the most successful models are focused on specific task domains. Recent advances include an increasing awareness of the necessity for detailed models of short-term retrieval, a theme reflected in a number of articles in the present collection.