Depression and implicit memory: a commentary.

In this invited commentary, we review four studies in which the issue of whether depression affects priming on implicit memory tests was examined. We conclude that a depressive mood does not affect amount of priming on several implicit memory tests under conditions in which marked effects are shown on conscious recollection (explicit memory). The mood congruity effect (depressives remember depression-related words better than controls; controls remember other types of material better than depressives) also largely disappears on perceptual implicit memory tests. We speculate about reasons for discrepancies in the literature, relate the findings to some current theories of individual differences in memory, and suggest some directions for future research.     

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 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 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 across eye blinks

The effect of eye blinks on short-term memory was examined in two experiments. On each trial, participants viewed an initial display of coloured, oriented lines, then after a retention interval they viewed a test display that was either identical or different by one feature. Participants kept their eyes open throughout the retention interval on some blocks of trials, whereas on others they made a single eye blink. Accuracy was measured as a function of the number of items in the display to determine the capacity of short-term memory on blink and no-blink trials. In separate blocks of trials participants were instructed to remember colour only, orientation only, or both colour and orientation. Eye blinks reduced short-term memory capacity by approximately 0.6–0.8 items for both feature and conjunction stimuli. A third, control, experiment showed that a button press during the retention interval had no effect on short-term memory capacity, indicating that the effect of an eye blink was not due to general motoric dual-task interference. Eye blinks might instead reduce short-term memory capacity by interfering with attention-based rehearsal processes.     

Short-term memory processes in counting

Four experiments examined the memory processes used to maintain location in a counting sequence. In Experiment 1, subjects who rapidly counted forward omitted many repeated-digit numbers (e.g., 77), as found previously with backward counting. Subjects in Experiment 2 counted backward with normal auditory feedback or with headphones through which white noise was channeled. In both cases, repeated-digit errors predominated, suggesting that the contents of short-term memory, rather than auditory sensory memory, are checked during counting. In Experiment 3, subjects silently wrote counting responses, and the omission errors resembled those in vocal counting. Repetition errors were also found and attributed to phonological recoding failures. Articulatory suppression in Experiment 4 greatly increased the number of repetition errors in the written counting task. A model of the counting process was proposed according to which subjects keep track of their location in the counting sequence by monitoring phonologically coded short-term memory representations of the numbers.     

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 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 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 in the rhesus monkey: A behavioral analysis of delayed-response performance

This study obtained quantitative data on the bodily orientations of rhesus monkeys in a delayed-response task and determined whether such orientations mediate the correct response in a choice trial. The basic task was a two-key chain schedule with the key leading to food signaled in the initial component. During the subsequent delay interval, the signal was removed, but it was necessary that one of the keys be pressed to advance the schedule to the terminal choice component. The position of the key pressed thus indicated orientation during the delay interval. When the monkeys had free access to the left and right keys, they tended to press the key leading to food throughout the chain schedule components and received food on more than 85% of the trials, even when the delay was extended to 20 seconds. However, when orientation toward the food key was disrupted by forcing the monkeys to press an extraneous center key during the delay, choice performance deteriorated. Requiring the center key presses early, rather than late, in the delay component had a strong disruptive effect. The relation of the results to the mediating coding-response hypothesis is discussed.     

Short-term visual memory for location in depth: A U-shaped function of time

Short-term visual memory was studied by displaying arrays of four or five numerals, each numeral in its own depth plane, followed after various delays by an arrow cue shown in one of the depth planes. Subjects reported the numeral at the depth cued by the arrow. Accuracy fell with increasing cue delay for the first 500 ms or so, and then recovered almost fully. This dipping pattern contrasts with the usual iconic decay observed for memory traces. The dip occurred with or without a verbal or color–shape retention load on working memory. In contrast, accuracy did not change with delay when a tonal cue replaced the arrow cue. We hypothesized that information concerning the depths of the numerals decays over time in sensory memory, but that cued recall is aided later on by transfer to a visual memory specialized for depth. This transfer is sufficiently rapid with a tonal cue to compensate for the sensory decay, but it is slowed by the need to tag the arrow cue’s depth relative to the depths of the numerals, exposing a dip when sensation has decayed and transfer is not yet complete. A model with a fixed rate of sensory decay and varied transfer rates across individuals captures the dip as well as the cue modality effect.     

Short-term episodic memory for visual textures: a roving probe gathers some memory

Cognition is shaped by the way that past experiences are represented in memory. To examine the representation of recent visual experiences, we devised a novel procedure that measures episodic recognition memory for synthetic textures. On each trial, two brief study stimuli were followed by a probe, which either replicated one of the study stimuli or differed in spatial frequency from both. The probe's spatial frequency roved from trial to trial, testing recognition with a range of differences between probe and study items. Repeated testing of recognition generated mnemometric functions, snapshots of memory strength's distribution. The distributional characteristics of the mnemometric functions rule out several hypotheses about memory representation, including the hypothesis that representations are prototypes constructed from previously seen stimuli; instead, stimuli are represented in memory as noisy exemplars.