Effects of exposure to psychophysical scaling on lingual vibrotactile magnitude estimation and magnitude production

The purpose of the present study was to determine if the results obtained by the scaling methods of magnitude estimation and magnitude production could be influenced by providing subjects with prior exposure to psychophysical scaling in the form of magnitude estimation or magnitude production. Group 1 (n = 10, Mage = 21.1 yr.) performed lingual vibrotactile-magnitude estimation followed by lingual vibrotactile magnitude production. Group 2 (n = 10, Mage = 19.7 yr.) performed lingual vibrotactile-magnitude production (using the magnitude-estimation responses provided by Group 1), followed by lingual vibrotactile-magnitude estimation. For the magnitude estimations there was no over-all statistically significant difference between the two groups, but there was for the magnitude-production values. Magnitude-estimation scaling was apparently not influenced by prior exposure to magnitude production, while magnitude-production scaling was influenced by prior exposure to magnitude estimation. The results are discussed in terms of how subjective scaling behavior in psychophysical experimentation may be influenced by the interaction between an absolute internal scaling mechanism and parameters set by the experimenter, such as scaling method and range of stimulus intensity.     

Effects of reinforcement magnitude on interval and ratio schedules

Rats' lever pressing was studied on three schedules of reinforcement: fixed interval, response-initiated fixed interval, and fixed ratio. In testing, concentration of the milk reinforcer was varied within each session. On all schedules, duration of the postreinforcement pause was an increasing function of the concentration of the preceding reinforcer. The running rate (response rate calculated by excluding the postreinforcement pauses) increased linearly as a function of the preceding magnitude of reinforcement on fixed interval, showed slight increases for two of the three animals on response-initiated fixed interval, and did not change systematically on fixed ratio. In all cases, the overall response rate either declined or showed no effect of concentration. The major effect of increasing the reinforcement magnitude was in determining the duration of the following postreinforcement pause, and changes in the response rate reflected this main effect.     

Effects of pointing direction and direction predictability on event-related lateralizations of the EEG

In two experiments, we investigated hemispheric electroencephalography (EEG) differences in 9(12) healthy volunteers during pointing to lateral and central targets. The questions addressed were whether horizontal pointing direction and the predictability of pointing direction modulated hemispheric differences (event-related lateralizations of the EEG = ERLs). To vary pointing direction predictability, targets were displayed either randomly at one of nine different positions on a screen (random) or at the same horizontal position in five subsequent trials (sequenced) while vertical positions varied randomly. Event-related lateralizations (ERLs) varied with pointing direction. This was true across changes in target eccentricity and pointing distance. Foci of the ERLs were in premotor and posterior parietal cortex, which might reflect the critical involvement of these areas in the control of visually guided reaching. Direction predictability reduced the parietal and premotor ERL before pointing onset, probably reflecting a lesser effort in visuomotor transformation. Predictability also added an overlying N2pc component to the early ERL after target onset and increased direction effects during movement.     

Segregation of study items in memory determines the magnitude and direction of directed forgetting

When words at study are divided into to‐be‐remembered and to‐be‐forgotten ones, people recall more of the former than of the latter in a surprise memory test for all words. In this study, we also tapped memory for word identity at study (forget or remember) by asking participants to reproduce in memory selected portions of the original words. We found word identity to be parasitic on word reproduction. As a result, there is a noted tendency to recall forget‐words from study as remember‐words in the memory test more than vice versa.     

Effects of reinforcement magnitude on choice and rate of responding

Behavior is sometimes insensitive, and sometimes extremely sensitive, to changes in reinforcement magnitude. The present work attempted to analyze this disparity by comparing, in a single experimental situation, a pigeon's choices with its response rates. Whereas choices varied directly with reinforcement duration, rates of responding were comparatively insensitive to duration changes. These results suggest that the effect of reinforcement magnitude on responding partly depends upon the extent to which responding influences the amount of reinforcement.     

Effects of reinforcement magnitude on spontaneous recovery.

Extinction of operant behavior has been associated with a number of undesirable effects. One such effect is the temporary reappearance of behavior after responding appears to be completely extinguished, known as spontaneous recovery. In this report, the occurrence of spontaneous recovery and its attenuation with large amounts of reinforcement were examined during the treatment of disruption.     

Dichotic listening in children: age-related changes in direction and magnitude of ear advantage

Children between the ages of 5 and 12 years were tested with dichotic listening tests utilizing single syllable words and random presentations of digits. They produced a higher prevalence of left ear dominance than expected, especially among right-handed children when tested with words. Whether more children demonstrate the LEA because of right hemisphere dominance for language or because there is less stability in ear advantage direction at younger ages cannot be fully resolved by this study. When ear advantages were measured by subtracting each child's lower score from the higher score without regard to right or left direction, an age-related trend toward lower measures of ear advantage was evident. This trend was greater for dichotic words than for dichotic digits. Structural factors that may be related to these results and possible influences of attention and verbal workload on the two kinds of dichotic stimuli are discussed.     

Effects of food deprivation and reinforcement magnitude on conditioned suppression

In Experiment I, the responding of rats lever pressing on a variable-interval schedule for sucrose solution was partially suppressed by a variable duration conditioned stimulus followed by shock. When food deprivation was increased, response rates during and before the conditioned stimulus increased monotonically. Varying the concentration of sucrose across blocks of sessions or from session to session in a semi-random sequence had little effect on response rates either before or during the conditioned stimulus. With a fixed sequence of increasing concentrations across a five-session block, increased concentration produced much more rapid increases in response rates before than during the conditioned stimulus. In Experiment II, rats were presented with the same sequence of increasing concentrations across a five-session block. When tested at 80% body weight, response rates increased rapidly as concentration increased, but at 100%, body-weight rates increased only slightly. The effect of a change in body weight in Experiment II thus mimicked the effect of the conditioned stimulus in the latter part of Experiment I. These findings support the view that the effect of a pre-aversive conditioned stimulus is similar to that of a change in food deprivation, but unlike that of a change in reinforcement magnitude.     

Effects of contextual and local factors on Ponzo illusion magnitude

Ponzo illusion has been explained by considering either just the inducing elements present in a restricted area of the visual field, the same area in which the test elements are located, or the stimulus configuration as a whole in which even the most distal figural elements – i.e., the external converging lines, here called “Ponzo wedge”– play a crucial role. The two studies reported here aimed at showing that both global configurational characteristics and inducing elements locally interacting with the test stimuli can independently affect the illusory effect. This hypothesis was tested using stimuli in which graphic-inducing elements giving rise to a herringbone pattern (Coren & Girgus, 1978) were drawn in the same area of the test segments. Results of Exp. 1 confirmed the effect of the two factors. In particular, both factors proved to determine the illusion, since they induced illusory effects either in isolation or in the same/opposite direction. In Exp. 2 the relative weight of these two factors was evaluated in relation to the width of the angle of the inducing elements and to the distance of the test segments from the vertex. Results showed no linear relationships between the distance of the test segments from the external inducing elements and the weight of the Ponzo wedge factor. Received: 25 June 1996 / Accepted: 1 October 1997     

The magnitude of binocular disparity modulates search time for targets defined by a conjunction of depth and colour

Nakayama and Silverman (1986) proposed that, when searching for a target defined by a conjunction of color and stereoscopic depth, observers partition 3D space into separate depth planes and then rapidly search each such plane in turn, thereby turning a conjunctive search into a "feature" search. In their study, they found, consistent with their hypothesis, shallow search slopes when searching depth planes separated by large binocular disparities. Here, the authors investigated whether the search slope depends upon the extent of the stereoscopically induced separation between the planes to be searched (i.e., upon the magnitude of the binocular disparity. The obtained slope shows that (1) a rapid search only occurs with disparities greater than 6 min of arc, a value that vastly exceeds the stereo threshold, and that (2) the steepness of this slope increases in a major way at lower disparities. The ability to implement the search mode envisaged by Nakayama and Silverman is thus clearly limited to large disparities; less efficient search strategies are mandated by lower disparity values, as under such conditions items from one depth plane may be more likely to "intrude" upon the other. (PsycINFO Database Record (c) 2008 APA, all rights reserved).     

Effects of aging on the magnitude and accuracy of quality-of-encoding judgments

Age invariance in monitoring associative learning has been the norm in numerous investigations concerning how accurately people predict future recall, predictions that are based partly on people's beliefs about forgetting. In this study, we obtained a measure of monitoring that is minimally influenced by beliefs about forgetting. Participants made quality-of-encoding (QUE) judgments by rating how well each item had been encoded. In 2 experiments, older and younger adults studied 60 paired-associate items; immediately after studying each one, they made a QUE judgment. Each item was presented at a 4-s or 8-s presentation rate. QUEs from both age groups were sensitive to the production of different strategies, presentation rate, and item characteristics. Reliable age differences in the correlation of QUEs and subsequent recall were found for related items but not for unrelated items. The outcomes indicate similar processes for generating QUE judgments by older and younger adults, but they also suggest the possibility of an age-related deficit in the accuracy of monitoring encoding in some experimental conditions.     

Vection during conflicting multisensory information about the axis, magnitude, and direction of self-motion

We examined the vection induced by consistent and conflicting multisensory information about self-motion. Observers viewed displays simulating constant-velocity self-motion in depth while physically oscillating their heads left-right or back-forth in time with a metronome. Their tracked head movements were either ignored or incorporated directly into the self-motion display (as an added simulated self-acceleration). When this head oscillation was updated into displays, sensory conflict was generated by simulating oscillation along: (i) an orthogonal axis to the head movement; or (ii) the same axis, but in a non-ecological direction. Simulated head oscillation always produced stronger vection than 'no display oscillation'--even when the axis/direction of this display motion was inconsistent with the physical head motion. When head-and-display oscillation occurred along the same axis: (i) consistent (in-phase) horizontal display oscillation produced stronger vection than conflicting (out-of-phase) horizontal display oscillation; however, (ii) consistent and conflicting depth oscillation conditions did not induce significantly different vection. Overall, orthogonal-axis oscillation was found to produce very similar vection to same-axis oscillation. Thus, we conclude that while vection appears to be very robust to sensory conflict, there are situations where sensory consistency improves vection.     

Effects of magnitude of food reinforcement on free-operant response rates

In Experiment 1 rats were trained to press a lever on a variable-ratio schedule of food presentation and were then exposed to progressively increasing magnitudes of food reinforcement. Response running rates (rates exclusive of the postreinforcement pause) were found to increase as a function of increasing reinforcement magnitudes. The effect of reinforcement magnitude on response rates inclusive of the postreinforcement pause, however, was less pronounced. Increases in the magnitude of reinforcement were also found to increase the length of the postreinforcement pause. Rats in Experiment 2 were trained to respond on a chained differential-reinforcement-of-low-rate variable-ratio schedule, and were exposed to increasing magnitudes of reinforcement as in Experiment 1. Response running rates increased in the variable-ratio component but decreased in the other component of the schedule. The results are discussed with reference to incentive accounts of reinforcement and the action of reinforcement on the response units generated by the operative contingencies.