A molar entropy model of age differences in spatial memory

Two very-short-term-memory, spatial scanning aging experiments were conducted involving a graphics character as a target stimulus. On the probe portion of a trial, the stimulus was presented in the same position as it was on the target portion of the trial (i.e., a same trial) 50% of the time. However, on the remaining 50% of the trials, the probe stimulus was shifted (or transposed) 1, 2, or 3 positions to the right or left of the original presentation (target) position. In Experiment 1, exposure duration was manipulated. In Experiment 2, the number of potential target display positions was manipulated. For both experiments, older adults showed larger transposition distance effects than younger adults for errors. In the past (e.g., P.A. Allen, 1990, 1991), this effect has been attributed to higher levels of internal noise (entropy) in older than younger adults. This research provides converging operations to this contention by using statistical physics methods to rigorously compute the entropy in a molar neural network across age groups. After successfully fitting the statistical mechanics model to the data, the model is proved to have external validity by fitting a simplified version of it to an earlier spatial memory aging experiment reported by P. R. Bruce and J. F. Herman (1986). The results of both traditional reaction time and error rate analyses, as well as the entropy modeling analyses, indicated that older adults exhibited higher levels of entropy than did the younger adults and that this effect appeared to be generalized across processing stage.     

Age related changes in the control of attention in depth.

In 2 experiments, the authors examined the control of spatial attention in depth in advanced age. Observers viewed 2 sets of lines that overlapped in two-dimensional (2-D) space but that were presented at different depth locations. An exogenous cue indicated the depth at which a colored target line would appear. On some trials, a distracting colored element was also presented. The luminance of this distracter varied from high to low. For both older and younger adults, distractors slowed reaction time less if they were at a different depth from the target. This effect was more robust for older adults with low-luminance distractors, indicating an important role for target features as well as attentional control. Adding another feature (i.e., color) that distinguished between target and distracter reduced the effects of slowing shown by the older observers and eliminated the cost of low-luminance distractors for all observers. The results suggest that attentional control in depth is maintained in aging. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Letter position information and printed word perception: The relative-position priming constraint.

Six experiments apply the masked priming paradigm to investigate how letter position information is computed during printed word perception. Primes formed by a subset of the target's letters facilitated target recognition as long as the relative position of letters was respected across prime and target (e.g., "arict" vs. "acirt" as primes for the target "apricot"). Priming effects were not influenced by whether or not absolute, length-dependent position was respected (e.g., "a-ric-t" vs. "arict"/"ar-i-ct"). Position of overlap of relative-position primes (e.g., apric-apricot; ricot-apricot; arict-apricot) was found to have little influence on the size of priming effects, particularly in conditions (i.e., 33 ms prime durations) where there was no evidence for phonological priming. The results constrain possible schemes for letter position coding. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Adult age differences in attentional allocation during memory search.

Young and older adults performed a memory search task in which, before probe onset, a cue indicated which of 4 memory-set items the probe was most likely to be. Results were consistent with an attentional allocation model in which performance represents a weighted combination, across trials, of focused (i.e., selective) vs distributed attention. The model significantly underestimated the reaction time (RT) required by miscued trials, probably because of the response inhibition occurring on these trials. The degree to which Ss relied on focused attention was significantly greater for older adults than for young adults. The estimated time required to shift attention between memory-set items was equivalent for the 2 age groups. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Age differences in target identification as a function of retinal location and noise level: Examination of the useful field of view.

Foveal and peripheral target detection were compared in young adults (M age?=?22 years) and older adults (M age?=?66 years) who were optically corrected for the viewing distance. In a two-alternative, forced-choice task, target letters were presented at 0° to 10.5° from fixation. Targets were presented alone, flanked on each side by one noise element (i.e., nontarget letter), or embedded in a horizontal row of 19 noise elements. An Age?×?Noise Level?×?Eccentricity interaction was obtained, wherein age differences were largest for peripheral targets presented in noise. Slope analyses of latency data showed that the performance of young adults in the high-noise condition was most similar to that of older adults in the low-noise condition. At the functional level, results indicated that aging is associated with a restricted useful field of view. In addition, the data suggest that age differences in search can be described by a model in which older adults take smaller perceptual samples from the visual scene and scan these samples more slowly than do the young adults. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Influence of adult age on primary and secondary memory search.

Conducted 2 experiments with 25 19–29 yr olds, 26 62–85 yr olds, 30 18–32 yr olds, and 30 61–81 yr olds to compare young and elderly adults on the ability to search lists of words stored in primary memory (PM) and in secondary memory (SM). Exp I indicated that age differences in search performance were greatest under SM conditions. Older Ss, unlike the younger ones, appeared biased toward responding that probe items were not members of the memory sets stored in SM. As a result of this apparent bias, older Ss committed a large number of errors on trials in which the probe was a member of the memorized list (i.e., positive probe trials) yet few errors on the trials in which the probe was not a member of the list ( i.e., negative probe trials). The responses of older Ss to negative probe trials were more rapid than were those to positive probe trials. In Exp II, this pattern of responding was examined. It is concluded that age differences were involved in the ability to encode memory sets and transfer them from PM to SM as well as in the ability to retrieve information from SM prior to conducting a memory search. (18 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Inhibition in verbal working memory revealed by brain activation

There are many occasions in which humans and other animals must inhibit the production of some behavior or inhibit the processing of some internal representation. Success in inhibitory processing under normal circumstances can be revealed by the fact that certain brain pathologies render inhibitory processing ineffective. These pathologies often have been associated with damage to frontal cortex, including lateral and inferior aspects. We provide behavioral evidence of a verbal working memory task that, by hypothesis, engaged inhibitory processing, and we show (by using positron emission tomograpny) that the inhibitory processing is associated with a lateral portion of the left prefrontal cortex. The task in which subjects engaged was item-recognition: Four target letters were presented for storage followed, after a brief interval, by a probe letter that could match a target letter or not. On some trials, when the probe did not match a target letter and therefore required a "no" response, the probe had matched a target letter of the previous trial, so on these trials a "yes" response was prepotent and had to be inhibited, by hypothesis. Compared with a condition in which no prepotent response was created, this condition yielded brain activation in left inferior frontal gyrus, in the region of Brodmann's area 45.     

Dissociative prime–probe contextual similarity effects on negative priming and repetition priming: A challenge to episodic retrieval as a unified account of negative priming.

This study examined the dependence of repetition priming (RP) and negative priming (NP) as a function of prime–probe contextual similarity in a paradigm in which participants were required to respond to a letter flanked by incompatible distractor letters (e.g., ABA). Experiment 1 used prime and probe displays containing a pair of "+" symbols that were presented horizontally or vertically. Experiments 2 and 3 manipulated whether the letter triplets contained the "!" symbol. In all experiments, regardless of whether the RP trials were intermixed with the NP trials (Experiment 2) or not (Experiment 3), RP was stronger in the prime–probe similar conditions than in the prime–probe dissimilar conditions, but NP was independent of prime–probe contextual similarity. These findings suggest that NP is not necessarily stronger in conditions in which episodic retrieval of the prime is more likely. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Preserved Spatial Memory Over Brief Intervals in Older Adults.

Two studies compared young and older adults' memory for location information after brief intervals. Experiment 1 found that accuracy of intentional spatial memory for individual locations was similar in young and older participants for set sizes of 3 and 6. Both groups also encoded individual locations in relation to the larger configuration of locations. Experiment 2 showed that like young adults, older adults' latency to respond to a test probe in a letter working memory task was negatively influenced by spatial information that was irrelevant to the task. This interference effect indicated preserved incidental memory for spatial information in older adults. Together, these data suggest that initial encoding of spatial information for relatively small numbers of items is largely preserved in healthy older adults and that representations of spatial information persist over short intervals. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Destination memory impairment in older people.

Older adults are assumed to have poor destination memory—knowing to whom they tell particular information—and anecdotes about them repeating stories to the same people are cited as informal evidence for this claim. Experiment 1 assessed young and older adults' destination memory by having participants tell facts (e.g., “A dime has 118 ridges around its edge”) to pictures of famous people (e.g., Oprah Winfrey). Surprise recognition memory tests, which also assessed confidence, revealed that older adults, compared to young adults, were disproportionately impaired on destination memory relative to spared memory for the individual components (i.e., facts, faces) of the episode. Older adults also were more confident that they had not told a fact to a particular person when they actually had (i.e., a miss); this presumably causes them to repeat information more often than young adults. When the direction of information transfer was reversed in Experiment 2, such that the famous people shared information with the participants (i.e., a source memory experiment), age-related memory differences disappeared. In contrast to the destination memory experiment, older adults in the source memory experiment were more confident than young adults that someone had shared a fact with them when a different person actually had shared the fact (i.e., a false alarm). Overall, accuracy and confidence jointly influence age-related changes to destination memory, a fundamental component of successful communication. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The Effect of Perceptual Distinctiveness on the Prospective and Retrospective Components of Prospective Memory in Young and Old Adults.

In two experiments, the effect of perceptual distinctiveness of cues on prospective memory performance was examined. Young and older adults completed a visual search task with embedded prospective memory instructions. On each trial, participants were asked to indicate the position of a target letter in a letter string, unless either of two letters previously identified as prospective memory cues was presented. Each prospective cue was associated with a specific response. Perceptual distinctiveness was manipulated by spatially displacing a single letter. The prospective component (successful detection of the cue) and the retrospective memory component (recalling the correct response when a cue is detected) were measured separately. Perceptual displacement of cues modulated performance of the prospective component but not the retrospective component. Young adults successfully detected a larger proportion of cues (prospective component) than older adults. However, there were minimal effects of age and no effect of cue displacement on participants' ability to recall the intention once they detected a cue (retrospective component performance). Results are discussed within the context of current theoretical models of prospective memory. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Saccade target selection and object recognition: evidence for a common attentional mechanism

The spatial interaction of visual attention and saccadic eye movements was investigated in a dual-task paradigm that required a target-directed saccade in combination with a letter discrimination task. Subjects had to saccade to locations within horizontal letter strings left and right of a central fixation cross. The performance in discriminating between the symbols "E" and "E", presented tachistoscopically before the saccade within the surrounding distractors was taken as a measure of visual attention. The data show that visual discrimination is best when discrimination stimulus and saccade target refer to the same object; discrimination at neighboring items is close to chance level. Also, it is not possible, in spite of prior knowledge of discrimination target position, to direct attention to the discrimination target while saccading to a spatially close saccade target. The data strongly argue for an obligatory and selective coupling of saccade programming and visual attention to one common target object. The results favor a model in which a single attentional mechanism selects objects for perceptual processing and recognition, and also provides the information necessary for motor action.     

Aging and the depth of binocular rivalry suppression.

Two experiments were designed to examine the effect of aging on the strength of binocular rivalry suppression. To produce rivalry, orthogonally oriented sine-wave luminance gratings were presented dichoptically. The observers were then required either to discriminate the spatial location of a probe spot presented to the dominant or suppressed eye's view or to detect the presence or absence of the probe. The observers in the younger and older age groups exhibited typical rivalry suppression for both tasks (i.e., the probe was more difficult to detect or discriminate when presented to the suppressed eye), but the magnitude of the suppression was significantly larger in the older observers. This increased suppression that accompanies aging can be explained by a reduction in the inhibition produced by the binocular matching circuitry of S. R. Lehky and R. Blake's (1991) model. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Evidence of preliminary response preparation from a divided attention task.

In a divided attention situation, preliminary response activations produced by stimuli on one channel were revealed through their effects on responses to stimuli on a secondary probe channel. Subjects performed concurrent but independent four-choice reaction-time tasks using the same four response fingers (middle and index fingers on both hands). In the main task, targets were large and small Ss and Ts, and medium-sized Ss and Ts sometimes appeared as distractors. Targets in the probe task were squares differing in location. A response to a probe square was faster if a distractor letter presented just before it had the same name as the target letter corresponding to that square (i.e., assigned to the same response key) than if the distractor letter had a different name—a result indicating that distractor letters cause partial response preparation. The timecourse of the effect demonstrated that preparation was based on preliminary information about distractor name that was available before distractor size had been determined. The results support models in which response preparation can sometimes begin before stimulus recognition has finished. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Adult age differences in the effects of sentence context and stimulus degradation during visual word recognition.

I investigated adult age differences in the efficiency of feature-extraction processes during visual word recognition. Participants were 24 young adults (M age?=?21.0 years) and 24 older adults (M age?=?66.5 years). On each trial, subjects made a word/nonword discrimination (i.e., lexical decision) regarding a target letter-string that was presented as the final item of a sentence context. The target was presented either intact or degraded visually (by the presence of asterisks between adjacent letters). Age differences in lexical decision speed were greater for degraded targets than for intact targets, suggesting an age-related slowing in the extraction of feature-level information. For degraded word targets, however, the amount of performance benefit provided by the sentence context was greater for older adults than for young adults. It thus appears that an age-related deficiency at an early stage of word recognition is accompanied by an increased contribution from semantic context. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Anger management: Age differences in emotional modulation of visual processing.

Although positive and negative images enhance the visual processing of young adults, recent work suggests that a life-span shift in emotion processing goals may lead older adults to avoid negative images. To examine this tendency for older adults to regulate their intake of negative emotional information, the current study investigated age-related differences in the perceptual boost received by probes appearing over facial expressions of emotion. Visually-evoked event-related potentials were recorded from the scalp over cortical regions associated with visual processing as a probe appeared over facial expressions depicting anger, sadness, happiness, or no emotion. The activity of the visual system in response to each probe was operationalized in terms of the P1 component of the event-related potentials evoked by the probe. For young adults, the visual system was more active (i.e., greater P1 amplitude) when the probes appeared over any of the emotional facial expressions. However, for older adults, the visual system displayed reduced activity when the probe appeared over angry facial expressions. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Training older adults to search more effectively: Scanning strategy and visual search in dynamic displays.

The authors examined the ability of older adults to modify their search strategies to detect changes in dynamic displays. Older adults who made few eye movements during search (i.e., covert searchers) were faster and more accurate compared with individuals who made many eye movements (i.e., overt searchers). When overt searchers were instructed to adopt a covert search strategy, target detection performance increased to the level of natural covert searchers. Similarly, covert searchers instructed to search overtly exhibited a decrease in target detection performance. These data suggest that with instructions and minimal practice, older adults can ameliorate the cost of a poor search strategy. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Adults' Age-Related Differences in Adaptivity of Strategy Choices: Evidence From Computational Estimation.

Four experiments document adults' age-related changes in computational estimation performance and in adaptivity of strategy choices (i.e., the ability to choose the most precise strategy on each trial). Young and older adults were asked to provide estimates of 2-by-2-digit multiplication problems (e.g., 43 X 78) under varying conditions of speed and accuracy emphasis. The main findings showed that (a) older adults provided less accurate estimates and took more time to estimate, especially on the most difficult problems or when using harder strategies; (b) young and older adults had similar strategy preferences; and (c) older adults chose estimation strategies less adaptively than young adults. Implications of these findings for understanding strategic changes during adulthood in a wide variety of cognitive domains are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Interference and facilitation in spatial working memory: Age-associated differences in lure effects in the n-back paradigm.

Working memory (WM) declines prominently during normal aging. The mechanisms underlying this decline are not fully understood. The authors analyzed performance on 2 versions of a 2-back spatial WM task to assess younger and older adults' responses to lures (i.e., nontarget items that match an item earlier in the sequence but not at the current target lag). Results demonstrate lure interference effects that are particularly pronounced among older adults. At the same time, however, older adults showed facilitation for targets. Taken together, these findings suggest that the contribution of familiarity signals to WM performance increases during normal aging. (PsycINFO Database Record (c) 2010 APA, all rights reserved)