Acoustic memory and the perception of speech

The nature of acoustic memory and its relationship to the categorizing process in speech perception is investigated in three experiments on the serial recall of lists of syllables. The first study confirms previous reports that sequences comprising the syllables, bah, dah, and gah show neither enhanced retention when presented auditorily rather than visually, nor a recency effect—both occurred with sequences in which vowel sounds differed (bee, bih, boo). This was found not to be a simple vowel-consonant difference since acoustic memory effects did occur with consonant sequences that were acoustically more discriminable (sha, ma, ga and ash, am, ag). Further experiments used the stimulus suffix effect to provide evidence of acoustic memory, and showed (1), increasing the acoustic similarity of the set grossly impairs acoustic memory effects for vowels as well as consonants, and (2) such memory effects are no greater for steady-state vowels than for continuously changing diphthongs. It is concluded that the usefulness of the information that can be retrieved from acoustic memory depends on the acoustic similarity of the items in the list rather than on their phonetic class or whether or not they have “encoded” acoustic cues. These results question whether there is any psychological evidence for “encoded” speech sounds being categorized in ways different from other speech sounds.     

Iconic memory and visible persistence

There are three senses in which a visual stimulus may be said to persist psychologically for some time after its physical offset. First, neural activity in the visual system evoked by the stimulus may continue after stimulus offset (“neural persistence”). Second, the stimulus may continue to be visible for some time after its offset (“visible persistence”). Finally, information about visual properties of the stimulus may continue to be available to an observer for some time after stimulus offset (“informational persistence”). These three forms of visual persistence are widely assumed to reflect a single underlying process: a decaying visual trace that (1) consists of afteractivity in the visual system, (2) is visible, and (3) is the source of visual information in experiments on decaying visual memory. It is argued here that this assumption is incorrect. Studies of visible persistence are reviewed; seven different techniques that have been used for investigating visible persistence are identified, and it is pointed out that numerous studies using a variety of techniques have demonstrated two fundamental properties of visible persistence: theinverse duration effect (the longer a stimulus lasts, the shorter is its persistence after stimulus offset) and theinverse intensity effect (the more intense the stimulus, the briefer its persistence). Only when stimuli are so intense as to produce afterimages do these two effects fail to occur. Work on neural persistences is briefly reviewed; such persistences exist at the photoreceptor level and at various stages in the visual pathways. It is proposed that visible persistence depends upon both of these types of neural persistence; furthermore, there must be an additional neural locus, since a purely stereoscopic (and hence cortical) form of visible persistence exists. It is argued that informational persistence is defined by the use of the partial report methods introduced by Averbach and Coriell (1961) and Sperling (1960), and the term “iconic memory” is used to describe this form of persistence. Several studies of the effects of stimulus duration and stimulus intensity upon the duration of iconic memory have been carried out. Their results demonstrate that the duration of iconic memory is not inversely related to stimulus duration or stimulus intensity. It follows that informational persistence or iconic memory cannot be identified with visible persistence, since they have fundamentally different properties. One implication of this claim that one cannot investigate iconic memory by tasks that require the subject to make phenomenological judgments about the duration of a visual display. In other words, the so-called “direct methods” for studying iconic memory do not provide information about iconic memory. Another implication is that iconic memory is not intimately tied to processes going on in the visual system (as visible persistence is); provided a stimulus is adequately legible, its physical parameters have little influence upon its iconic memory. The paper concludes by pointing out that there exists an alternative to the usual view of iconic memory as a precategorical sensory buffer. According to this alternative, iconic memory is post-categorical, occurring subsequent to stimulus identification. Here, stimulus identification is considered to be a rapid automatic process which does not require buffer storage, but which provides no information about episodic properties of a visual stimulus. Information about these physical stimulus properties must, in some way, be temporarily attached to a representation of the stimulus in semantic memory; and it is this temporarily attached physical information which constitutes iconic memory.     

Stimulus exposure time and perceptual memory

The recent explosion of research on implicit memory has facilitated the examination of perceptual and conceptual processes in the encoding of information. Nevertheless, stimulus exposure time—the amount of time that a stimulus is physically available to a perceiver’s scrutiny—has received little attention. In the present paper, we examine the effect of stimulus exposure time on three implicit memory measures (word-fragment completion, perceptual identification, and general knowledge) and two explicit memory measures (graphemic cued recall and semantic cued recall). In Experiment 1, we demonstrated that increases in exposure time lead to increases in implicit perceptual memory, but not to implicit conceptual memory, when the encoding task focuses on perceptual features of the stimulus. We replicated this effect in Experiment 2 and demonstrated that increases in exposure time lead to increases in perceptualand conceptual memory when the measures are explicit. Thus, the current experiments demonstrate that manipulations of exposure time lead to dissociations in implicit, but not explicit, memory.     

Anatomic and environmental dimensions of stimulus-response compatibility: implication for theories of memory coding.

Reaction time was higher when the relation between stimulus location and anatomic hand was reversed (e.g., left light-right hand) rather than direct (e.g., left light-left hand), even though the environmental location of the hand (up or down) was unrelated to the location of the stimulus (left or right). This effect was shown to be due primarily to decision processes, rather than to interhemisphere transfer delay. This result does not support the view that long-term memory for responses encodes environmental but not anatomic dimensions.     

Decision processes in children's recognition memory

Kindergarteners and third graders were given a continuous recognition memory task involving two-digit numbers. In addition, a rating scale consisting of photographs of various facial expressions was used to obtain confidence judgments from the Ss. Conventional analyses as well as signal detection analyses of the data revealed the following results: (a) the overall performance of the third graders was superior to that of the kindergarteners; (b) memory strength decreased as the number of intervening items increased; (c) there was no difference in the forgetting rates of the two grade levels; (d) the third graders exhibited a more liberal response bias than the kindergarteners; (e) both the hit rate (probability of correctly labeling an old stimulus as old) and the false-alarm rate (probability of incorrectly labeling a new stimulus as old) increased across blocks of items; (f) the increases in the hit rate and the false-alarm rate over blocks were due to a change in criterion from a relatively conservative level to a more lenient one; (g) the lower the S's level of confidence in judging an item as old, the lower was the probability of that item actually being old; (h) the third graders were better than the kindergarteners at gauging the accuracy of their recognition responses. It was concluded that with respect to recognition memory, chidren as young as $\text{5}\text{1}\text{2}$ years old are capable, to some extent, of monitoring their own memory states.     

Regional cerebral blood flow response to recognition memory versus semantic classification tasks

Two randomly assigned groups, N = 7 each, of neurologically normal patients were composed. One group, RM, had regional cerebral blood flow measurements during a recognition memory probe test; the other group, SC, had rCBF measurements during a semantic classification task, using the same stimulus and response features as the RM task. Thus, the groups differed only in the cognitive instruction they were executing. The RM group showed a significantly lower change from resting baseline to activation, in mean left hemisphere initial slope index, than did the SC group. The RM group, but not the SC group, showed a significant inverse correlation between occipital flow and accuracy of memory performance as indicated by d′. Correlations between age and hemispheric initial slope index, and between homologous left and right hemisphere sites, were also described. The results are considered to support an anatomical basis for the distinction between episodic and semantic memory and to suggest that occipital flow may diminish with accurate memory performance because of an upstream demand of blood in the medial temporal lobes.     

The influence of spatial pattern on visual short-term memory for contrast

Several psychophysical studies of visual short-term memory (VSTM) have shown high-fidelity storage capacity for many properties of visual stimuli. On judgments of the spatial frequency of gratings, for example, discrimination performance does not decrease significantly, even for memory intervals of up to 30 s. For other properties, such as stimulus orientation and contrast, however, such “perfect storage” behavior is not found, although the reasons for this difference remain unresolved. Here, we report two experiments in which we investigated the nature of the representation of stimulus contrast in VSTM using spatially complex, two-dimensional random-noise stimuli. We addressed whether information about contrast per se is retained during the memory interval by using a test stimulus with the same spatial structure but either the same or the opposite local contrast polarity, with respect to the comparison (i.e., remembered) stimulus. We found that discrimination thresholds got steadily worse with increasing duration of the memory interval. Furthermore, performance was better when the test and comparison stimuli had the same local contrast polarity than when they were contrast-reversed. Finally, when a noise mask was introduced during the memory interval, its disruptive effect was maximal when the spatial configuration of its constituent elements was uncorrelated with those of the comparison and test stimuli. These results suggest that VSTM for contrast is closely tied to the spatial configuration of stimuli and is not transformed into a more abstract representation.     

Hemispheric memory for random forms revisited

Hemispheric short-term memory was studied by projecting complex random forms that varied in their verbal association strength to the left and right hemispheres. Male and female subjects responded same or different to a centrally presented memory test stimulus which occurred 0, 5, 10, or 20 sec after the target item. Reaction time for both response judgments was significantly shorter for right-hemisphere presentations over all memory intervals. For both performance measures, response judgment interacted with the length of memory interval and the verbal association value of the stimulus items. No hemispheric differences were observed as a function of subject sex. Hemispheric memory for complex forms appears primarily dependent upon task processing demands rather than stimulus factors when response time is used to measure recognition under tightly controlled conditions.     

Release of inattentional blindness by high working memory load: elucidating the relationship between working memory and selective attention

An unexpected stimulus often remains unnoticed if attention is focused elsewhere. This inattentional blindness has been shown to be increased under conditions of high memory load. Here we show that increasing working memory load can also have the opposite effect of reducing inattentional blindness (i.e., improving stimulus detection) if stimulus detection is competing for attention with a concurrent visual task. Participants were required to judge which of two lines was the longer while holding in working memory either one digit (low load) or six digits (high load). An unexpected visual stimulus was presented once alongside the line judgment task. Detection of the unexpected stimulus was significantly improved under conditions of higher working memory load. This improvement in performance prompts the striking conclusion that an effect of cognitive load is to increase attentional spread, thereby enhancing our ability to detect perceptual stimuli to which we would normally be inattentionally blind under less taxing cognitive conditions. We discuss the implications of these findings for our understanding of the relationship between working memory and selective attention.     

Recognition hypermnesia: The growth of recognition memory (d') over time with repeated testing

This study sought to determine whether recognition hypermnesia (unforgetting) might be obtained over time with repeated testing of recognition memory. Four types of stimuli were investigated: pictures or words (captions) from configured (funny) or non-configured (non-funny) cartoons. Three recognition tests, each comprising the same stimulus and distractor items, were successively administered after the presentation of a large set of captioned cartoons. Silent think intervals of 5 min were interpolated between recognition tests. Recognition hypermnesia, measured by increasing d' estimates of accessible recognition memory, was obtained with the pictures from configured (funny) cartoons but not with any of the other groups.     

Arousal,valence, and memory for detail

A common finding in the emotion‐memory literature is that memory is enhanced for positively arousing stimuli and negatively arousing stimuli relative to neutral stimuli. We tested the notion that post‐stimulus elaboration is responsible for these effects. Post‐stimulus elaboration refers to the process of thinking about an event (after its offset) more frequently or more in‐depth. We tested the hypothesis by presenting participants with 36 slides depicting events that varied in arousal (low and high) and valence (positive and negative). The opportunity for elaboration was manipulated by requiring participants, during the inter‐slide interval, to complete addition problems, simply view the addition problems, or view a blank slide. Cued recall memory was tested for central and background details. Based on the post‐stimulus elaboration hypothesis it was expected that the greatest memory decline would occur for the central details of negatively and positively arousing slides when participants were required to complete addition problems (i.e., a distractor task × arousal × detail interaction). Contrary to the hypothesis, we found that filling the inter‐slide interval with a distractor task decreased memory for negative stimuli compared to positive stimuli. This effect was independent of arousal. We also found that arousal increased central detail memory for positive and negative stimuli and background detail memory for positive stimuli but not for negative stimuli. This interaction was explained on the basis of pre‐attentive encoding and cue utilisation. It was concluded that in order to understand the complex relationship between emotion and memory, future studies should include, as a minimum, the variables of valence, arousal, and detail.     

Long-term memory of hierarchical relationships in free-living greylag geese

Animals may memorise spatial and social information for many months and even years. Here, we investigated long-term memory of hierarchically ordered relationships, where the position of a reward depended on the relationship of a stimulus relative to other stimuli in the hierarchy. Seventeen greylag geese (Anser anser) had been trained on discriminations between successive pairs of five or seven implicitly ordered colours, where the higher ranking colour in each pair was rewarded. Geese were re-tested on the task 2, 6 and 12 months after learning the dyadic colour relationships. They chose the correct colour above chance at all three points in time, whereby performance was better in colour pairs at the beginning or end of the colour series. Nonetheless, they also performed above chance on internal colour pairs, which is indicative of long-term memory for quantitative differences in associative strength and/or for relational information. There were no indications for a decline in performance over time, indicating that geese may remember dyadic relationships for at least 6 months and probably well over 1 year. Furthermore, performance in the memory task was unrelated to the individuals’ sex and their performance while initially learning the dyadic colour relationships. We discuss possible functions of this long-term memory in the social domain.     

Interrogative suggestibility,delayed memory and self-concept

This study investigates the relationship between interrogative suggestibility as measured by the Gudjonsson Suggestibility Scale (GSS) and variables related to memory recall and self-esteem. There were 30 Ss, tested twice 1 week apart. After completing the GSS they were required to fill in a number of Semantic Differential scales relating to the concepts: Myself as I am generally, Myself during the experiment and The experimenter. Ss were generally more suggestible during the second interview when their memory about the context of the interrogation context had deteriorated. The exception was that negative feedback appeared to have most effect on suggestibility and self-esteem the first time it was applied. Self-esteem related to ‘competence’ and ‘potency’ correlated significantly with suggestibility, especially during the first interrogative session. Perceptions of the experimenter were generally not found to be significantly related to suggestibility.     

Deconstructing the effect of self-directed study on episodic memory

Self-directed learning is often associated with better long-term memory retention; however, the mechanisms that underlie this advantage remain poorly understood. This series of experiments was designed to “deconstruct” the notion of self-directed learning, in order to better identify the factors most responsible for these improvements to memory. In particular, we isolated the memory advantage that comes from controlling the content of study episodes from the advantage that comes from controlling the timing of those episodes. Across four experiments, self-directed learning significantly enhanced recognition memory, relative to passive observation. However, the advantage for self-directed learning was found to be present even under extremely minimal conditions of volitional control (simply pressing a button when a participant was ready to advance to the next item). Our results suggest that improvements to memory following self-directed encoding may be related to the ability to coordinate stimulus presentation with the learner’s current preparatory or attentional state, and they highlight the need to consider the range of cognitive control processes involved in and influenced by self-directed study.     

A feature-segmentation model of short-term visual memory

A feature-segmentation model of short-term visual memory (STVM) for contours is proposed. Memory of the First stimulus is maintained until the second stimulus is observed. Three processes interact to determine the relationship between stimulus and response: feature encoding, memory, and decision. Basic assumptions of the model are twofold: (i) the STVM system divides a contour into convex parts at regions of concavity; and (ii) the value of each convex part represented in STVM is an independent Gaussian random variable. Simulation showed that the five-parameter fits give a good account of the effects of the four experimental variables. The model provides evidence that: (i) contours are successfully encoded within 0.5 s exposure, regardless of pattern complexity; (ii) memory noise increases as a linear function of retention interval; (iii) the capacity of STVM, defined by pattern complexity (the degree that a pattern can be handled for several seconds with little loss), is about 4 convex parts; and (iv) the confusability contributing to the decision process is a primary factor in deteriorating recognition of complex figures. It is concluded that visually presented patterns can be retained in STVM with considerable precision for prolonged periods of time, though some loss of precision is inevitable.     

Place avoidance learning and memory in a jumping spider

Using a conditioned passive place avoidance paradigm, we investigated the relative importance of three experimental parameters on learning and memory in a salticid, Servaea incana. Spiders encountered an aversive electric shock stimulus paired with one side of a two-sided arena. Our three parameters were the ecological relevance of the visual stimulus, the time interval between trials and the time interval before test. We paired electric shock with either a black or white visual stimulus, as prior studies in our laboratory have demonstrated that S. incana prefer dark ‘safe’ regions to light ones. We additionally evaluated the influence of two temporal features (time interval between trials and time interval before test) on learning and memory. Spiders exposed to the shock stimulus learned to associate shock with the visual background cue, but the extent to which they did so was dependent on which visual stimulus was present and the time interval between trials. Spiders trained with a long interval between trials (24 h) maintained performance throughout training, whereas spiders trained with a short interval (10 min) maintained performance only when the safe side was black. When the safe side was white, performance worsened steadily over time. There was no difference between spiders tested after a short (10 min) or long (24 h) interval before test. These results suggest that the ecological relevance of the stimuli used and the duration of the interval between trials can influence learning and memory in jumping spiders.     

Recall memory for visually presented chess positions

A series of three experiments replicated and extended earlier research reported by Chase and Simon (1973), de Groot (1965), and Charness (Note 1). The first experiment demonstrated that the relationship between memory for chess positions and chess skill varies directly with the amount of chess-specific information in the stimulus display. The second experiment employed tachistoscopic displays to incrementally "build" tournament chess positions by meaningful or nonmeaningful chunks and demonstrated that meaningful piece groupings during presentation markedly enhance subsequent recall performance. The third experiment tested memory for one of two positions presented in immediate sequence and demonstrated that explanations based on a limited-capacity short-term memory (Chase & Simon, 1973) are not adequate for explaining performance on this memory task.     

“Being there” and remembering it: Presence improves memory encoding

Few studies have investigated the link between episodic memory and presence: the feeling of “being there” and reacting to a stimulus as if it were real. We collected data from 244 participants after they had watched the movie Avengers: Age of Ultron. They answered questions about factual (details of the movie) and temporal memory (order of the scenes) about the movie, as well as their emotion experience and their sense of presence during the projection. Both higher emotion experience and sense of presence were related to better factual memory, but not to temporal order memory. Crucially, the link between emotion and factual memory was mediated by the sense of presence. We interpreted the role of presence as an external absorption of the attentional focus toward the stimulus, thus enhancing memory encoding. Our findings could shed light on the cognitive processes underlying memory impairments in psychiatric conditions characterized by an altered sense of reality.     

Recognition memory and intelligence

The assumption that individual differences in recognition memory are associated with individual differences in intelligence was explored by administering intelligence tests and tests of immediate visual recognition memory to a sample of 52 5-year-old children expected to vary widely from one another in intelligence. Each child was given the Peabody Picture Vocabulary Test (Form L) and two tests of immediate recognition memory: one test for 27 abstract patterns and one test for 27 unfamiliar cartoon faces. The mean PPVT-IQ for the sample was in the average range at 98.1. Interindividual variability in IQ proved to be high as reflected in the group SD of 22.6, with scores ranging from 40 to 136. The recognition tasks proved to be of moderate difficulty. Individual differences in memory for patterns were highly related to memory for faces (r = .76), indicating that the overall recognition test was reliable. The most important result of the present study was the strong association between recognition memory performance and PPVT-IQ of .70. The relation between recognition memory and IQ could not be accounted for by the inclusion of a few very low IQ children, since the association remained high at .61 when children with IQs below 75 were omitted from analysis. In short, the present results indicate that immediate recognition memory is highly associated with intelligence.     

Updating memory using mnemonic devices

The process of memory updating enables people to recall information most recently associated with a particular stimulus context and to ignore or forget information previously associated with it. In a series of five experiments utilizing mnemonic devices it was found that when associative interference was maximized, only a limited disruption of updating resulted. In addition, mnemonic recall was not dependent on the utilization of higher-order memory components. However, support was found for the hypothesis that memory can be searched using temporal cues and for the idea that the size of the search set formed in memory is important. It was found that the older the event was to be recalled, the greater were the number of events in the search set and therefore the greater was the magnitude of the recall error. The size of the search set created in memory and the role of temporal-contextual cues in defining this search set may be important factors not only in mnemonic recall but in other types of learning and recall as well.