A signal detection analysis of memory for nonoccurrence in pigeons.

In a relatively unexplored memory procedure, pigeons indicated whether or not an event recently occurred. On positive trials, a sample stimulus was presented, followed by a delay, followed by a choice between the yes and no alternatives (with yes being the correct choice). On negative trials, the yes and no choice alternatives were presented without a preceding sample, and on these trials, no was the correct choice. Recent research on this topic seems to suggest that performance on negative trials is governed by a memory-free default response strategy, whereas performance on positive trials is governed by memory for the sample stimulus. However, a signal detection analysis leads to a different conclusion. In both cases, according to this account, performance was determined by the strength of a memory trace in relation to a decision criterion. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Tuning bandwidths for near-threshold stimuli in area MT

It is not known whether psychophysical performance depends primarily on small numbers of neurons optimally tuned to specific visual stimuli, or on larger populations of neurons that vary widely in their properties. Tuning bandwidths of single cells can provide important insight into this issue, yet most bandwidth measurements have been made using suprathreshold visual stimuli, whereas psychophysical measurements are frequently obtained near threshold. We therefore examined the directional tuning of cells in the middle temporal area (MT, or V5) using perithreshold, stochastic motion stimuli that we have employed extensively in combined psychophysical and physiological studies. The strength of the motion signal (coherence) in these displays can be varied independently of its direction. For each MT neuron, we characterized the directional bandwidth by fitting Gaussian functions to directional tuning data obtained at each of several motion coherences. Directional bandwidth increased modestly as the coherence of the stimulus was reduced. We then assessed the ability of MT neurons to discriminate opposed directions of motion along six equally spaced axes of motion spanning 180 degrees. A signal detection analysis yielded neurometric functions for each axis of motion, from which neural thresholds could be extracted. Neural thresholds remained surprisingly low as the axis of motion diverged from the neuron's preferred-null axis, forming a plateau of high to medium sensitivity that extended approximately 45 degrees on either side of the preferred-null axis. We conclude that directional tuning remains broad in MT when motion signals are reduced to near-threshold values. Thus directional information is widely distributed in MT, even near the limits of psychophysical performance. These observations support models in which relatively large numbers of signals are pooled to inform psychophysical decisions.     

Mechanisms of imagery-perception interaction.

A number of different research findings have shown that mental imagery can affect the perceptual processing of stimuli. The present research was aimed at characterizing the representations and processes underlying imagery–perception interactions. In 4 experiments, Ss mentally projected images of letters into the visual field, and either detected or detected and localized point threshold stimuli that fell on or off the image. Stimuli falling on the image were detected more often than stimuli falling off the image, consistent with the hypothesis that the representations at the interface between imagery and perception have an array format. When the facilitation was analyzed in terms of signal detection theory, it was found to consist only of criterion lowering, and not of enhanced sensitivity. The local criterion-lowering effect of imaged letters was then compared with the effect of perceiving a letter and attending to a letter. Perceiving a letter had no discernible effect on stimulus detection, whereas attending to the letter caused the same local criterion lowering, without sensitivity changes, as imaging the letter. This is consistent with the claims of U. Neisser (1976) and others that imagery is an attentional state. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A principal components analysis of dynamic spatial memory biases.

Research has shown that spatial memory for moving targets is often biased in the direction of implied momentum and implied gravity, suggesting that representations of the subjective experiences of these physical principles contribute to such biases. The present study examined the association between these spatial memory biases. Observers viewed targets that moved horizontally from left to right before disappearing or viewed briefly shown stationary targets. After a target disappeared, observers indicated the vanishing position of the target. Principal components analysis revealed that biases along the horizontal axis of motion loaded on separate components from biases along the vertical axis orthogonal to motion. The findings support the hypothesis that implied momentum and implied gravity biases have unique influences on spatial memory. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

"Where did I go wrong?" A psychophysiological analysis of error detection.

There is a component of the event-related brain potential, the error-related negativity (or ERN), that is related to error detection in choice reaction time (RT) tasks. The J. Miller (1982) paradigm was used to determine whether the detection process manifested by the ERN involves a comparison between representations of the actual response and the correct response or between representations of the stimulus anticipated by the S and the stimulus that actually occurs. The data favored the former rather than the latter kind of comparison, with the magnitude of the error signal depending on the similarity or dissimilarity between the two response representations. In turn, response similarity depended on the strategy used by the Ss to select responses: Response parameters selected first defined which responses would be most similar. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Statistical properties of d ' and β estimates of signal detection theory.

This study provides practical guidelines for estimating and performing inferential tests using sensitivity, d', and response bias, β, estimates of signal detection theory obtained in single-participant designs. In a Monte Carlo study, statistical bias and sampling variability of these estimates were examined across a wide range of distributional overlap. Two factors were manipulated: N (number of presentations of each stimulus) and C (decision criterion along the perceptual axis). Both d' and β estimates were relatively unbiased with small sampling variance for N values of at least 100; for smaller N values, both were positively biased. The d' estimates remained unaffected by C, and β estimates were unaffected by the means of the signal?+?noise distribution (effectively d') throughout their estimable ranges. Limiting cases and recommendations for use are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

On the nature of the decision axis in signal-detection-based models of recognition memory.

Most models of recognition memory involve a signal-detection component in which a criterion is placed along a decision axis. Older models generally assume a familiarity-decision axis, but newer models often assume a likelihood ratio axis instead because it allows for a more natural account of the ubiquitous mirror effect. In 3 experiments reported here, item strength was differentially manipulated to see whether a mirror effect would occur. Within a list, the items from 1 category were strengthened by repetition, but the items from another category were not. On the subsequent recognition test, the hit rate was higher for the strong category, but the false-alarm rates for the weak and strong categories were the same (i.e., no mirror effect was observed). This result suggests that the decision axis represents a familiarity scale and that participants adopt a single decision criterion that they maintain throughout the recognition test. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Contrast detection in noise: a new method for assessing the visual function in cataract

The detectability of a signal decreases in the presence of externally added visual noise. A linear relation exists between the energy of a signal at threshold and the spectral density of the added visual noise. This relation, represented by contrast detection in noise function, allows a given loss in contrast sensitivity (CS) to be attributed to an increase in the internal intrinsic noise and/or a decrease in the detection efficiency of the observer. Intrinsic noise gives a measure of the random background noise within the visual system, whereas detection efficiency is a measure of how effectively the observer utilizes the available stimulus information. Recent work shows that neural dysfunction produces a decrease in the detection efficiency, whereas optical deficits produce a change in the intrinsic noise only. We investigated whether the CS loss in cataract can be attributed to either a change in intrinsic noise, in detection efficiency, or both. Contrast detection in noise functions was measured for 10 uniocular cataract patients. Comparison between the two eyes showed no significant difference in detection efficiency, although the intrinsic noise increased significantly in the cataractous eye. The data suggest that detection efficiency may provide a measure of neural visual function behind a cataract and, conversely, that intrinsic noise provides a measure of the visual effect of the cataract itself. We discuss the implications of intrinsic noise as a measure of cataract for both clinical assessment and research.     

On the difference between strength-based and frequency-based mirror effects in recognition memory

According to the standard signal-detection model of recognition memory, confidence judgments for recognition responses are reached in much the same way that old-new decisions are reached (i.e., on the basis of criteria situated along the strength-of-evidence axis). The question investigated here is how the confidence criteria shift when recognition accuracy is manipulated across conditions. Although several theories assume that the old-new decision criterion shifts when recognition accuracy changes, less is known about how the confidence criteria move. An analysis of data previously reported by R. Ratcliff, G. McKoon, and M. Tindall (1994) and some new data reported here suggest that the confidence criteria fan out on the decision axis as d' decreases. This result is qualitatively consistent with the predictions of a likelihood ratio model, although the data did not support the stronger quantitative predictions of this account.     

Sequence Effects in the Categorization of Tones Varying in Frequency.

In contrast to exemplar and decision-bound categorization models, the memory and contrast models described here do not assume that long-term representations of stimulus magnitudes are available. Instead, stimuli are assumed to be categorized using only their differences from a few recent stimuli. To test this alternative, the authors examined sequential effects in a binary categorization of 10 tones varying in frequency. Stimuli up to 2 trials back in the sequence had a significant effect on the response to the current stimulus. The effects of previous stimuli interacted with one another. A memory and contrast model, according to which only ordinal information about the differences between the current stimulus and recent preceding stimuli is used, best accounted for these data (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Decision rules for recognition memory confidence judgments.

According to the standard signal-detection model of recognition memory, confidence judgments for recognition responses are reached in much the same way that old-new decisions are reached (i.e., on the basis of criteria situated along the strength-of-evidence axis). The question investigated here is how the confidence criteria shift when recognition accuracy is manipulated across conditions. Although several theories assume that the old-new decision criterion shifts when recognition accuracy changes, less is known about how the confidence criteria move. An analysis of data previously reported by R. Ratcliff, G. McKoon, and M. Tindall (1994) and some new data reported here suggest that the confidence criteria fan out on the decision axis as d' decreases. This result is qualitatively consistent with the predictions of a likelihood ratio model, although the data did not support the stronger quantitative predictions of this account. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Physiological memory in primary auditory cortex: characteristics and mechanisms

"Physiological memory" is enduring neuronal change sufficiently specific to represent learned information. It transcends both sensory traces that are detailed but transient and long-term physiological plasticities that are insufficiently specific to actually represent cardinal details of an experience. The specificity of most physiological plasticities has not been comprehensively studied. We adopted receptive field analysis from sensory physiology to seek physiological memory in the primary auditory cortex of adult guinea pigs. Receptive fields for acoustic frequency were determined before and at various retention intervals after a learning experience, typified by single-tone delay classical conditioning, e.g., 30 trials of tone-shock pairing. Subjects rapidly (5-10 trials) acquire behavioral fear conditioned responses, indexing acquisition of an association between the conditioned and the unconditioned stimuli. Such stimulus-stimulus association produces receptive field plasticity in which responses to the conditioned stimulus frequency are increased in contrast to responses to other frequencies which are decreased, resulting in a shift of tuning toward or to the frequency of the conditioned stimulus. This receptive field plasticity is associative, highly specific, acquired within a few trials, and retained indefinitely (tested to 8 weeks). It thus meets criteria for "physiological memory." The acquired importance of the conditioned stimulus is thought to be represented by the increase in tuning to this stimulus during learning, both within cells and across the primary auditory cortex. Further, receptive field plasticity develops in several tasks, one-tone and two-tone discriminative classical and instrumental conditioning (habituation produces a frequency-specific decrease in the receptive field), suggesting it as a general process for representing the acquired meaning of a signal stimulus. We have proposed a two-stage model involving convergence of the conditioned and unconditioned stimuli in the magnocellular medial geniculate of the thalamus followed by activation of the nucleus basalis, which in turn releases acetylcholine that engages muscarinic receptors in the auditory cortex. This model is supported by several recent findings. For example, tone paired with NB stimulation induces associative, specific receptive field plasticity of at least a 24-h duration. We propose that physiological memory in auditory cortex is not "procedural" memory, i.e., is not tied to any behavioral conditioned response, but can be used flexibly.     

Alternative therapies: abuses of scientific method and challenges to dental research

Research with the mismatch negativity component of event-related potentials has uncovered a system that detects change in the acoustic environment on an automatic basis. The system is considered to compare incoming stimuli to representations of the past and to emit an MMN if change is detected. Previous investigations have shown that the relevant memory of the past can become dormant and then be reactivated by a reminder stimulus. It is unclear, however, whether what is reactivated is an holistic representation of stimuli or separate representations of features of stimuli. The present study provides data that supports the latter possibility but leaves open the former one.     

The comparison of visual working memory representations with perceptual inputs.

The human visual system can notice differences between memories of previous visual inputs and perceptions of new visual inputs, but the comparison process that detects these differences has not been well characterized. In this study, the authors tested the hypothesis that differences between the memory of a stimulus array and the perception of a new array are detected in a manner that is analogous to the detection of simple features in visual search tasks. That is, just as the presence of a task-relevant feature in visual search can be detected in parallel, triggering a rapid shift of attention to the object containing the feature, the presence of a memory–percept difference along a task-relevant dimension can be detected in parallel, triggering a rapid shift of attention to the changed object. Supporting evidence was obtained in a series of experiments in which manual reaction times, saccadic reaction times, and event-related potential latencies were examined. However, these experiments also showed that a slow, limited-capacity process must occur before the observer can make a manual change detection response. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Comparison requirements and attention in identical-nonidentical stimulus discriminations.

Perceptual matching data show several puzzling effects. Particularly problematic are the disparities between the processing rates for same and different stimuli—the fast–same effect—and between the processing rates for two same–different judgment tasks that are related as mirror images—the task effect. Current models have difficulty accounting simultaneously for both effects. Central to these models is a stimulus comparison process that derives relative judgments of sameness and difference from tests of the congruence of stimulus representations. A contrasting view holds that same–different judgments can be modeled as absolute, rather than relative, judgments. This latter view is shown to be supported by experimental data. Reaction times (RTs) for judgments of identical letter strings increase with string length at the same rate whether judgments are based on all the information in the strings or just the information in a single pair of component letters. The data show that stimulus comparisons of the sort described by previous models are not involved in these judgments. An attentional model accounts for the data and for the fast–same and task effects as well. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The structure of somatosensory information for human postural control

The goal of the present study was to determine the properties of the somatosensory stimulus that alter its temporal coupling to body sway. Six standing subjects were tested while touching a metal plate positioned either directly in front of or lateral to the subject. In each condition, the plate moved 4 mm at 0.2 Hz in either the medial-lateral (ML) or anterior-posterior direction (AP). The results showed that coupling between body sway and touch plate movement was strongest when the touch plate moved in a direction along the longitudinal axis of the arm. Coupling strength was weaker when the touch plate moved perpendicular to the longitudinal axis of the arm. The results consistently show that a radial expansion stimulus was more effective than a lamellar-type stimulus at the fingertip. Moreover, somatosensory information from a surface is interpreted in terms of the orientation of the contact limb and the potential degrees of freedom available through its movement.     

Attentional capture with rapidly changing attentional control settings.

The classic theory of spatial attention hypothesized 2 modes, voluntary and involuntary. Folk, Remington, and Johnston (1992) reported that even involuntary attention capture by stimuli requires a match between stimulus properties and what the observer is looking for. This surprising conclusion has been confirmed by many subsequent studies. In these studies, however, the observer typically looks for the same property throughout an entire session. Real-world behavior, in contrast, often requires frequent shifts in attentional set. The present study examined whether such shifts weaken attentional settings, allowing task-irrelevant objects to capture attention. Surprisingly, fluctuating control settings did not increase vulnerability to capture by salient stimuli (color singletons and abrupt onsets). We conclude that the attention control system is remarkably flexible, able to rapidly and fully adopt new settings and abandon old settings. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Speed, size, and edge-rate information for the detection of collision events.

In the present study an alternative analysis to τ? was considered that was based on perceived speed and size and that assumed constant deceleration for the detection of collision events. Observers were presented with displays simulating a 3-D environment with obstacles in the path of observer motion. During the trial, observer motion decelerated at a constant rate and was followed by a blackout prior to the end of the display. Observers had to detect which trials resulted in a collision. The results indicate that collision detection varied as a function of the size of the obstacles, observer speed, and edge rate—findings not predicted by an analysis of τ?. The results suggest that observers use an analysis based on speed and size information. A model that assumes constant deceleration is proposed for braking control. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Dissociations between reaction times and temporal order judgments: A diffusion model approach.

A diffusion model for simple reaction time (RT) and temporal order judgment (TOJ) tasks was developed to account for a commonly observed dissociation between these 2 tasks: Most stimulus manipulations (e.g., intensity) have larger effects in RT tasks than in TOJ tasks. The model assumes that a detection criterion determines the level of sensory evidence needed to conclude that a stimulus has been presented. Analysis of the performance that would be achieved with different possible criterion settings revealed that performance was optimal with a lower criterion setting for the TOJ task than for the RT task. In addition, the model predicts that effects of stimulus manipulations should increase with the size of the detection criterion. Thus, the model suggests that commonly observed dissociations between RT and TOJ tasks may simply be due to performance optimization in the face of conflicting task demands. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Patients with schizophrenia demonstrate dissociation between affective experience and motivated behavior.

Self-reported emotional experience does not differ between patients with schizophrenia and healthy individuals, suggesting that the anhedonia in schizophrenia instead reflects decoupling of affect from motivated behavior. In 2 behavioral conditions, participants with schizophrenia and healthy participants were able to prolong or decrease exposure to stimuli while stimuli were present or alter the likelihood of future exposure to stimuli on the basis of internal representations. They also provided self-reports of affective experience. Patients showed weaker correspondence between behavior and ratings than did comparison participants. The effect was amplified when patients responded on the basis of internal rather than evoked stimulus representations. These data suggest that the motivational deficits in schizophrenia reflect problems in the ability to translate experience into action. (PsycINFO Database Record (c) 2010 APA, all rights reserved)