Response latencies in human matching-to-sample

Optimum characterization of individual information-processing skills requires isolation of assessable components. In matching-to-sample, three elementary processes might be separated if a proposed model of serial, selfterminating search were supported: registration of the stimulus in short-term memory, comparison of the two registered stimuli, and execution of the identifying response. Support for the model was obtained when response latencies were examined as a function of left-to-right position of the target stimulus in a display, but quantitative estimates of components could not be made because of interactions between tasks and the linearity of the scanning process. A second experiment, which varied the number of comparison stimuli, yielded highly linear functions whose slopes and intercepts violated certain aspects of the model. Data on eye movements obtained in a third experiment again supported the basic model but indicated that median response latencies represent a confounding of optimal and suboptimal performances.     

Response latencies in naming objects

After some preliminary analysis of what is involved in naming objects, in which the possible role of classificatory systems in the memory store is discussed, it is shown experimentally that there are consistent differences between the times taken to respond to presented objects by uttering their names, variations between the performances of different individuals being outweighed by variations due to the different objects. Moreover, there is a high consistency between different individuals as to the ordering of objects in respect of their naming latencies. It is further shown that a high correlation exists between the time taken to name an object and the frequency with which its name occurs in the language as a whole, as estimated in the Thorndike-Lorge Word List. Some implications of these findings are discussed, especially with reference to possible mechanisms by which presented objects are visually identified, and the appropriate names retrieved from the “word-store.”     

Response amendment latencies during discrete arm movements

Examinations of the ability to rapidly modify ongoing movements have found that amendment latencies are shorter when a visual stimulus specifies an increase in movement velocity as compared to when a movement reversal is required. Our present study examined the hypothesis that amendment latencies for both continue and reverse instructions are dependent on the muscle activation state when the amendment is produced. Visual stimuli representing continue and reverse instructions wer represented at four different phases of a discrete arm movement, with amendment latencies measured to modified electromyographic (EMG) patterns. Amendment latencies for the continue instruction were shortest when the stimulus was presented early in the movement and increased when the stimulus was presented later in the response. The opposite trend was true for the reversal condition with long latencies occurring when the stimulus was presented early in the movement. Our findings support the notion that amendment latencies are directly related to the active state of the motor system when the modification is required, and the nature of the amendment to be generated.     

Response latencies of rats during behavioral thermoregulation

The cutaneous thermal stimulation that elicits behavioral thermoregulatory behavior was investigated in these experiments. In Experiment I, rats were placed in a cool environment and allowed to barpress for 3-sec bursts of radiant heat reinforcement. In various phases of the study, rats could earn different intensities of anterior, posterior, or whole-body radiation. Identical response rates were exhibited at each intensity for all exposure conditions; this information, when considered with existing literature on behavioral and neurophysiological studies, suggests that the rat’s thermoregulatory behavior depends on information carried by nonmyelinated fibers that supply thermoreceptors in the skin. Experiment II investigated the hypothesis that cooling of the skin is the stimulus that elicits each thermoregulatory response. Time series measures of skin temperature fluctuations and reaction times (RTs) were obtained. Tails of the RT distributions were shown to conform to exponential probability density functions, and mean RT varied linearly over the domain of reinforcement intensities used. A computer simulation model that describes temperature gradients across layers of skin was employed to estimate temperature fluctuations at the level of the cool receptors. Comparison of simulated skin temperatures with obtained RTs suggests that momentary thermoregulatory behavior is controlled mainly by cooling skin temperature.     

False memory in a short-term memory task

The Deese/Roediger-McDermott (DRM; Roediger & McDermott, 1995) paradigm reliably elicits false memories for critical nonpresented words in recognition tasks. The present studies used a Sternberg (1966) task with DRM lists to determine whether false memories occur in short-term memory tasks and to assess the contribution of latency data in the measurement of false memories. Subjects studied three, five, or seven items from DRM lists and responded to a single probe (studied or nonstudied). In both experiments, critical lures were falsely recognized more often than nonpresented weak associates. Latency data indicated that correct rejections of critical lures were slower than correct rejections of weakly related items at all set sizes. False alarms to critical lures were slower than hits to list items. Latency data can distinguish veridical and false memories in a short-term memory task. Results are discussed in terms of activation-monitoring models of false memory.     

Tactile short-term memory

Subjects tried to recall the location of a tactile stimulus on the underside of the forearm after delays of 0, 3, 5, 10, 15, 30, 45 and 60 sec. When “rehearsal” was prevented by requiring subjects to count backwards during the delay, accuracy of recall decreased systematically reaching an asymptote after 45 sec. When subjects were left free to “rehearse,” this did not affect the decline in accuracy over the first 10 sec. Between 10 and 15 sec. there was a significant increase in accuracy followed by a slow decline which had not reached asymptote by 60 sec. It is suggested that tactile STM (short-term memory) depends on two processes, a fading sensory trace which is unaffected by distraction and a less labile system which does not appear to be verbal but which depends on “rehearsal.”     

Distinguishing short-term memory from working memory

The aim of the present research was to determine whether short-term memory and working memory could be distinguished. In two studies, 7- to 13-year-olds (N = 155, N = 132) were administered tasks thought to assess short-term memory as well as tasks thought to assess working memory. Both exploratory and confirmatory factor analyses distinguished short-term memory tasks from working memory tasks. In addition, performance on working memory tasks was related to word decoding skill but performance on short-term memory tasks was not. Finally, performance on both short-term memory and working memory tasks were associated with age-related increases in processing speed. Results are discussed in relation to models of short-term and working memory.     

Response latencies and the computerized assessment of intelligence

A study was undertaken to examine the relationship between response latencies to verbal ability test items administered by computer and overall verbal intelligence test scores. Sixty-four undergraduate students responded to a test of verbal ability under four conditions of alternate test forms (A or B) and modes of administration (computerized vs paper-and-pencil). The response latencies recorded during computerized testing, averaged for each subject, showed a negative correlation with overall test scores as would be predicted from a speed-of-information-processing perspective of human intelligence (Jensen, 1982a, b; Vernon, 1983). This inverse relationship was evident in every condition of test form and mode of administration, thereby demonstrating the generalizability of these findings. Discussion considered the implications of test speededness for the results of this study and provided suggestions for future research employing response latency data as a means for studying the cognitive processes underlying intelligent behaviour.     

Binding in short-term visual memory

The integration of complex information in working memory, and its effect on capacity, shape the limits of conscious cognition. The literature conflicts on whether short-term visual memory represents information as integrated objects. A change-detection paradigm using objects defined by color with location or shape was used to investigate binding in short-term visual memory. Results showed that features from the same dimension compete for capacity, whereas features from different dimensions can be stored in parallel. Binding between these features can occur, but focused attention is required to create and maintain the binding over time, and this integrated format is vulnerable to interference. In the proposed model, working memory capacity is limited both by the independent capacity of simple feature stores and by demands on attention networks that integrate this distributed information into complex but unified thought objects.     

Intra-list differences in short-term memory

Subjects attempted to recall lists of nine consonants immediately after presentation. Using various recall orders it was found that recall of part of a list interfered with retention of the other parts, memory for items presented early in a list being less affected by such interference than was that for later items. Since this result was not obtained when rate of presentation was increased, it is suggested that rehearsal contributed to the greater stability of early items.     

Interference in short-term auditory memory

Although interference is a well-established forgetting function in short-term auditory memory, an adequate understanding of its underlying mechanisms and time course has yet to be attained. The present study therefore aimed to explore these issues in memory for timbre. Listeners compared standard and comparison complex tones, having distinct timbres (four components varying in frequency), over a 4.7-s retention interval and made a same–different response. This interval either was silent or included one of 15 distractor tones occurring 0 ms, 100 ms, or 1,200 ms after the standard. These distractors varied in the extent to which the frequencies of their component tones were shared with the standard. Performance in comparing the two tones was significantly impaired by distractors composed of novel frequencies, regardless of the temporal position at which the distractor occurred. These results were fully compatible with the recent timbre memory model (McKeown & Wellsted, 2009 McKeown, D. and Wellsted, D. 2009. Auditory memory for timbre. Journal of Experimental Psychology: Human Perception and Performance, 35: 855–875. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]) and suggested that interference in auditory memory operates via a feature-overwriting mechanism.     

Redundancy effects in short-term memory

Five experiments are reported whose purpose was to demonstrate that short-term memory is improved by redundancy within the material. In Experiment I “tune” containing two, three, four and five tones of differing frequencies had to be coded into digits 1-5, to indicate the order of the pitches in a tune. Performance on stimuli containing correlated amplitude and duration were compared with the uni-dimensional condition. Experiment II repeated I, but required intensity to be coded. Experiment III required pitch coding under three conditions including that when amplitude and frequency were uncorrelated, and compared the performance of musically trained sunjects with nonmusicians. Experiment IV repeated III, but subjects were informed of the relation between dimensions. Experiment V involved “shadowing” the tunes by whistling simultaneously with the stimulus.

It was concluded (a) that intercorrelation improves, but zero correlation impairs short-term memory; (b) that knowledge of the relation between dimensions improves performance in the correlated condition, but does not prevent impairment under zero correlation; and (c) the performance of musically trained subjects exceeds that of controls and is unaffected by the presence of a correlated or uncorrelated dimension.     

Context in verbal short-term memory

We tested the hypothesis that stimulus-related contextual information that is incidental to task demands-an episodic code-is automatically, obligatorily encoded and stored as a part of short-term memory (STM) representations. Four experiments employed a running span task to investigate the effects of manipulating two types of contextual information: stimulus grouping and color. Three experiments established that grouping context effects are sensitive neither to volitional control nor to task difficulty and that they generalize across testing procedures (yes/no recognition and immediate serial recall). A fourth experiment demonstrated an effect of manipulating the congruity of the color of stimuli between study and test. These demonstrations of the robustness and generality of context effects in STM are consistent with the predictions of the episodic coding model of STM.     

Interference effects in short-term memory

Abstract.— Two experiments exploring the modality relation between memory task and interference task are reported. With visual and verbal tasks, variations in modality relation did not influence the total amount recalled. The usual serial position effect was observed when memory and interference task were of different modalities. The amount of recall was found to be a function of the memory strategies used by the subjects, 'active' strategies producing highest recall.