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Biomedical subjects

J Myerson

Publications and source records attributed to J Myerson.

34 records · Page 2Linked to original sources
PubMed1992

General slowing in semantic priming and word recognition.

Analyses of lexical decision studies revealed that (a) older (O) adults' mean semantic priming effect was 1.44 times that of younger (Y) adults, (b) regression lines describing the relations between older and younger adults' latencies in related (O = 1.54 Y-112 and unrelated conditions (O = 1.50 Y-93) were not significantly different, and (c) that there was a proportional relation between older and younger adults' priming effects (O = 1.48 Y-2). Analyses of word-naming studies yielded similar results. Analyses of delayed pronunciation data (Balota & Duchek, 1988) revealed that word recognition was 1.47 times slower in older adults, whereas older adults' output processes were only 1.26 times slower. Overall, analyses of whole latencies and durations of component processes provide converging evidence for a general slowing factor of approximately 1.5 for lexical information processing.

Adult↗
PubMed1991

How general is general slowing? Evidence from the lexical domain.

Three analyses are reported that are based on data from 19 studies using lexical tasks and a reduced version of the Hale, Myerson, and Wagstaff (1987) nonlexical data set. The results of Analysis 1 revealed that a linear function with a slope of approximately 1.5 described the relationship between the lexical decision latencies of older (65-75 years) and younger (19-29 years) adults. The results of Analysis 2, based on response latencies from 6 lexical tasks other than lexical decision, revealed a virtually identical linear relationship. In Analysis 3, it was found that performance on nonlexical tasks spanning the same range of task difficulty was described by a significantly steeper regression line with a slope of approximately 2.0. These findings suggest that although general cognitive slowing is observed in both domains, the degree of slowing is significantly greater in the nonlexical domain than in the lexical domain. In addition, these analyses demonstrate how the meta-analytic approach may be used to determine the limits to the external validity of experimental findings.

Adult↗
PubMed1991

General cognitive slowing in the nonlexical domain: an experimental validation.

Older and younger adults were tested on 4 nonlexical tasks: choice reaction time, letter classification, mental rotation, and abstract matching. A positively accelerated relation was observed between older and younger adults' latencies. Consistent with general slowing, the relation observed with the same subjects in each condition was more than 3 times as precise as in a comparable meta-analysis. Further analyses compared the ability of various models to describe the present data and also to predict the data on the basis of parameters estimated from a previous meta-analysis. Compared with linear models, the information-loss and overhead models provided more accurate accounts of general cognitive slowing in the nonlexical domain.

Adult↗
PubMed1990

The information-loss model: a mathematical theory of age-related cognitive slowing.

A model of cognitive slowing is proposed with the following assumption: Information is lost during processing, processing occurs in discrete steps with step duration inversely related to the amount of information currently available, and the effect of aging is to increase the proportion of information lost per step. This model correctly predicts a positively accelerated relation between latencies of older and younger adults and provides a unified account of the effects of task complexity, practice, speed-accuracy tradeoffs, and fluctuations in individual performance. Strong support for the thesis that cognitive slowing is global, and not localized in specific age-sensitive components, is provided by the fact that the model accurately predicts the latencies of older adults on the basis of those of younger adults, without regard to the nature of the task, across a latency range of nearly 2 orders of magnitude.

Adult↗
PubMed1989

Global increase in response latencies by early middle age: complexity effects in individual performances.

Ten young women (age 20 to 22 years) and 10 middle-aged women (age 36 to 44 years) served as subjects in choice reaction time, letter classification, and abstract matching-to-sample tasks. In each of seven conditions, the older group responded more slowly than the younger group. Age differences showed a complexity effect. That is, differences between the latencies of young and old subjects increased as the latency of the young subjects increased. Both linear and power functions accurately described the relation between the latencies of the middle-aged and young adult groups. This was true not only for the relation between average latencies but also for the relation between corresponding quartiles of latency distributions. Similar results were observed at the individual level: All middle-aged subjects showed complexity effects, and, for each middle-aged subject, the relation between her latencies and those of the average young adult was well described by linear and power functions. These findings indicate that age-related slowing is apparent by age 40, and that complexity effects are observable in individual performances. This slowing is global and not specific to particular tasks, as indicated by the fact that the latencies of older adults can be predicted directly from those of younger adults without regard to the nature of the task.

Adult↗
PubMed1988

Age, variability, and speed: between-subjects diversity.

Two independent data sets were selected to examine the interrelations among reaction time (RT), between-subject variability or diversity (SD), and age. In both data sets, a strong correlation between RT and SD was obtained. This strong correlation was not affected when age was controlled in a partial correlation analysis. On the other hand, a weaker but significant correlation was obtained between age and SD. This correlation was eliminated when RT was controlled in a partial correlation analysis. Our analyses of the two data sets also indicated that the relation between RT and SD is identical for both young and elderly groups. Thus, the greater diversity often observed in performances of older groups is a direct consequence of slowing, rather than an independent effect of advancing age.

Adolescent↗
PubMed1988

Choice in transition: A comparison of melioration and the kinetic model.

Transition-state choice behavior of pigeons was examined in two experiments designed to test predictions of melioration and the kinetic model. Both experiments began with an initial training condition during which subjects were maintained on concurrent variable-interval schedules. In Experiment 1, subjects were then exposed to concurrent variable-ratio schedules, whereas in Experiment 2, subjects were then exposed to concurrent extinction. Contrary to the predictions of melioration, but consistent with the kinetic model, acquisition of preference on concurrent variable-ratio schedules followed a negatively accelerated logistic trajectory, and preference remained stable in concurrent extinction. Predictions made by the kinetic model concerning rates of switching between alternatives were also supported.

Journal Article↗
PubMed1987

General slowing of nonverbal information processing: evidence for a power law.

Data were analyzed from studies of nonverbal information processing in which the dependent measure was the latency of pressing or releasing a response key. Positively-accelerated power functions described the relationship between the response latencies of groups of older (50 to 60 years and 65 to 75 years) and younger adults (20 to 25 years) with extreme precision (r2 = .99). The exponent of the best-fitting power function increased with the age of the older group. The form of the relationship is allometric, and is consistent with a model (Botwinick, 1984) in which response latency increases exponentially with task difficulty. The present findings suggest that this model holds across a wide variety of information-processing tasks and over a very broad range of latencies.

Adult↗
PubMed1984

Practical implications of the matching law.

Many problem situations in applied settings are best conceptualized as choice situations. In addition, applied behavior analysts create choice situations when they reinforce a competing response to decrease inappropriate behavior. When such situations are analyzed using the matching law, variable interval (VI) schedules of reinforcement prove to be a superior intervention strategy regardless of the nature of the schedule maintaining other, less appropriate behavior. This conclusion is robust in that VI schedule superiority is observed in situations in which choice behavior is highly biased or shows pronounced undermatching as well as those in which the matching law holds precisely. Our analysis demonstrates the potential practical value of mathematical descriptions of behavior.

Journal Article↗
PubMed1979

Automaintenance without stimulus-change reinforcement: Temporal control of key pecks.

Yoked pairs of experimentally naive pigeons were exposed to a modified autoshaping procedure in which key pecking by the leader birds postponed both keylight termination and access to grain for the leader and the follower bird. Key pecking developed and was maintained in all birds and continued through two reversals of roles in the yoked procedure. Although temporal control developed more slowly in follower birds, asymptotic temporal distributions of key pecking were similar for all birds in both leader and follower roles; maximum responding occurred soon after keylight onset and decreased to a minimum prior to reinforcement. Response distributions for both leader and follower birds were described by Killeen's (1975) mathematical model of temporal control. Follower birds received response-independent reinforcement, and the development by these birds of temporal distributions which are minimal immediately prior to reinforcement is without precedent in Pavlovian appetitive conditioning. However, maintenance of key pecking by the leader birds, whose responses postponed both stimulus-change and food reinforcement, supports an interpretation of autoshaped and automaintained key pecking as responding elicited by signaled grain presentation.

Journal Article↗
PubMed1977

Magnification in striate cortex and retinal ganglion cell layer of owl monkey: a quantitative comparison.

Magnification, the relative size of the neural representation of a portion of the visual field, decreases more rapidly with increasing visual field eccentricity in striate cortex than in the retinal ganglion cell layer of the owl monkey (Aotus trivirgatus); the proportion of the cells in striate cortex devoted to central vision is much larger than the comparable proportion of retinal ganglion cells. Magnification in striate cortex is a power function of magnification in the retinal ganglion cell layer. A formula for convergence (ganglion cells to cortical neurons) follows from this relationship.

Animals↗
PubMedDate not supplied

The effects of eye and limb movements on working memory.

Three experiments examined the role of eye and limb movements in the maintenance of information in spatial working memory. In Experiment 1, reflexive saccades interfered with memory span for spatial locations but did not interfere with memory span for letters. In Experiment 2, three different types of eye movements (reflexive saccades, pro-saccades, and anti-saccades) interfered with working memory to the same extent. In all three cases, spatial working memory was much more affected than verbal working memory. The results of these two experiments suggest that eye movements interfere with spatial working memory primarily by disrupting processes localised in the visuospatial sketchpad. In Experiment 3, limb movements performed while maintaining fixation produced as much interference with spatial working memory as reflexive saccades. These results suggest that the interference produced by eye movements is not the result of their visual consequences. Rather, all spatially directed movements appear to have similar effects on visuospatial working memory.

Extremities↗