Verbal self-reports about matching to sample: effects of the number of elements in a compound sample stimulus.

Adults' self-reports about their choices in a delayed matching-to-sample task were studied as a function of the number of elements (one, two, or three) in a compound sample stimulus. Signal-detection analyses were used to examine control of self-reports by the number of sample elements, by the speed and accuracy of choices reported about, and by several events contingent on self-reports. On each matching-to-sample trial, a sample element appeared as one of two comparison stimuli. Choice of the matching element, if made within 500 ms of the onset of the comparison stimuli, produced points worth money or chances in a drawing for money, depending on the subject. After each choice, subjects pressed either a "yes" or "no" button to answer a computer-generated query about whether the choice met the point contingency. The number of sample elements in the matching-to-sample task varied across trials, and events contingent on self-reports varied across experimental conditions. In Experiment 1, the conditions were defined by different combinations of feedback messages and point consequences contingent on self-reports, but self-reports were systematically influenced only by the sample-stimulus manipulation. Self-report errors increased with the number of sample elements. False alarms (inaccurate reports of success) were far more common than misses (inaccurate reports of failure), and false alarms were especially likely after choices that were correct but too slow to meet the point contingency. Sensitivity (A') of self-reports decreases as the number of sample elements increased. In addition, self-reports were more sensitive to choice accuracy than to choice speed. All subjects showed a pronounced bias (B'H) for reporting successful responses, although the bias was reduced as the number of sample elements increased and successful choices became less frequent. Experiment 2 demonstrated that the failure of point contingencies to influence self-reports in the first experiment was not due to a general ineffectiveness of the point consequences. Rates of inaccurate self-reports decreased when they resulted in point losses and increased when they resulted in point gains.     

Bias in self-evaluation: Signal probability effects

Two experiments examined apparent signal probability effects in simple verbal self-reports. After each trial of a delayed matching-to-sample task, young adults pressed either a “yes” or a “no” button to answer a computer-presented query about whether the most recent choice met a point contingency requiring both speed and accuracy. A successful matching-to-sample choice served as the “signal” in a signal-detection analysis of self-reports. Difficulty of matching to sample, and thus signal probability, was manipulated via the number of nonmatching sample and comparison stimuli. In Experiment 1, subjects exhibited a bias (log b) for reporting matching-to-sample success when success was frequent, and no bias or a bias for reporting failure when success was infrequent. Contingencies involving equal conditional probabilities of point consequences for “I succeeded” and “I failed” reports had no systematic effect on this pattern. Experiment 2 found signal probability effects to be evident regardless of whether referent-response difficulty was manipulated in different conditions or within sessions. These findings indicate that apparent signal probability effects in self-report bias that were observed in previous studies probably were not an artifact of contingencies intended to improve self-report accuracy or of the means of manipulating signal probability. The findings support an analogy between simple self-reports and psychophysical judgments and bolster the conclusion of Critchfield (1993) that signal probability effects can influence simple self-reports much as they do reports about external stimuli in psychophysical experiments.     

Sample-stimulus discriminability and sensitivity to reinforcement in delayed matching to sample

Five pigeons were trained in a delayed matching-to-sample task with red and green stimuli. The retention interval between sample-stimulus presentation and the availability of the choice stimuli was varied between 0.01 s and 12 s within each session. The probability of food produced by correct-red and correct-green responses was varied across conditions. Sample-stimulus discriminability and response bias were measured at four different retention intervals. The results of these analyses showed an interaction between the discriminability of the sample stimuli and the control exerted by differential reinforcement. At longer retention intervals, sample discriminability decreased and sensitivity of choice behavior to changes in the red/green reinforcer ratio increased. An analogous relation has been reported in conditional discriminations in which the physical disparity of stimuli has been varied. This correspondence suggests that increasing the delay between presentation of one of two stimuli and an opportunity to respond discriminatively to it may be functionally similar to increasing the physical similarity of the two stimuli.     

Control of pigeons' matching-to-sample performance by differential sample response requirements

Pigeons were trained on a matching-to-sample task in which sample hue and required sample-specific observing behavior provided redundant, relevant cues for correct choices. On trials that involved red and yellow hues as comparison stimuli, a fixed-ratio 16 schedule (FR 16) was required to illuminate the comparisons when the sample was red, and a differential-reinforcement-of-low-rates 3-sec schedule (DRL 3-sec) was required when the sample was yellow. On trials involving blue and green hues as comparison stimuli, an FR 16 schedule was required when the sample was blue and a DRL 3-sec schedule was required when the sample was green. For some pigeons, a 0-sec delay intervened between sample offset and comparison onset, whereas other pigeons experienced a random mixture of 0-sec and 2-sec delay trials. Test trial performance at 0-sec delay indicated that sample-specific behavior controlled choice performance considerably more than sample hue did. Test performance was independent of whether original training involved all 0-sec delay trials or a mixture of 0-sec and 2-sec delays. Sample-specific observing response requirements appear to facilitate pigeons' matching-to-sample performance by strengthening associations between the observing response and correct choice.     

Choice Between Two Discrimination Tasks in Chimpanzees (Pan troglodytes)

The purpose of the present study was to investigate the effects of cognitive effort on a chimpanzee's choice between discrimination tasks. The tasks were of the matching-to-sample type. In Experiment 1, the chimpanzee was required to choose between a task providing a high reinforcement rate with high cognitive effort and a task providing a low reinforcement rate with low cognitive effort. Her choice depended on the reinforcement rate more than the cognitive effort. Experiments 2, 3, and 4 examined whether the kind of cognitive effort influenced the chimpanzee's choice. Experiment 2 manipulated the sample-choice relationship, so-called symmetry in the matching-to-sample tasks. Experiment 3 manipulated the number of comparison stimuli. Experiment 4 manipulated the delay interval between the sample and the comparison stimuli. In Experiments 2 and 3, the effects of the cognitive effort were confounded with those of the reinforcement rates. However, in one condition of Experiment 4, the chimpanzee preferred the simultaneous task to the delayed task, despite the lack of a significant difference in reinforcement rates between the two tasks. The present study demonstrated that the chimpanzee's choice of discrimination task depended on the cognitive effort involved, in addition to the reinforcement rate.     

Characteristics of forgetting functions in delayed matching to sample

Performance of pigeons in delayed matching-to-sample procedures was measured in terms of an index of discriminability derived from the difference between logarithms of ratios of choice responses to comparison stimuli following the different sample stimuli. Forgetting functions that plotted discriminability as a function of delay-interval duration were well described by a simple negative exponential function with two parameters, one describing initial discriminability of sample stimuli at zero delay (log d₀) and the other describing rate of decrement in discriminability with increasing delay-interval duration (b). With the difference between wavelength values of the comparison stimuli held constant, a large difference between wavelengths of the sample stimuli resulted in a higher log d₀ value than that for a small difference between sample stimuli, without changing the rate of decrement in discriminability, b. An increase in the fixed-ratio requirement for sample-key responding produced an increase in log d₀ without affecting b, and interpolation of ambient illumination in the delay interval increased b without influencing log d₀. Both parameters changed when intertrial-interval duration was varied. The result of variation in the point of interpolation of ambient illumination in the delay interval indicated that levels of discriminability at longer delays were independent of discriminability levels at earlier delays, consistent with the properties of the exponential function. Functions relating performance to delay-interval duration were suggested to have two characteristics: discriminability of the sample stimuli in the absence of a delay between the stimuli and the behavior they occasion, and rate of attenuation in discriminability with increasing delay-interval duration.     

Retrospective coding in pigeons' delayed matching-to-sample

In this study we examined how coding processes in pigeons' delayed matching-to-sample were affected by the stimuli to be remembered. In Experiment 1, two groups of pigeons initially learned 0-delay matching-to-sample with identical comparison stimuli (vertical and horizontal lines) but with different sample stimuli (red and green hues or vertical and horizontal lines). Longer delays were then introduced between sample offset and comparison onset to assess whether pigeons were prospectively coding the same events (viz., the correct line comparisons) or retrospectively coding different events (viz., their respective sample stimuli). The hue-sample group matched more accurately and showed a slower rate of forgetting than the line-sample group. In Experiment 2, pigeons were trained with either hues or lines as both sample and comparison stimuli, or with hue samples and line comparisons or vice versa. Subsequent delay tests revealed that the hue-sample groups remembered more accurately and generally showed slower rates of forgetting than the line-sample groups. Comparison dimension had little or no effect on performance. Together, these data suggest that pigeons retrospectively code the samples in delayed matching-to-sample.     

Forgetting in retarded and nonretarded persons under conditions of minimal strategy use

Short-term memory processes of mentally retarded (mild, moderate, and severe) and nonretarded persons were compared in a delayed matching-to-sample task that minimized the use of verbal rehearsal. In addition to trials with delays up to 20 s, the inclusion of trials on which the sample and comparison stimuli occurred simultaneously made it possible to isolate memory and discriminability. Forgetting was most pronounced between the simultaneous and 0-s conditions, and nonretarded subjects forgot less than retarded subjects between these conditions. There were no group differences beyond the 0-s delay. Ease of strategy use failed to account for individual differences, and reported strategy use was not related systematically to performance. These findings are incompatible with the hypothesis that normal-retarded differences occur only on tasks involving effortful cognitive strategies. Differences between nonretarded and retarded groups in this study may be due to a failure in automatic encoding processes in retarded persons.     

Intratrial proactive interference in pigeon short-term memory: Manipulation of stimulus dimension and dimensional similarity

Proactive interference was studied using an intratrial preparation in two delayed matching-to-sample experiments employing pigeons. On interference trials, an interfering sample and a target sample were presented successively and were followed by a test consisting of a choice between two stimuli, one associated with each sample. Control trials were identical to interference trials except that the interfering sample was not presented. On both types of trials, choice of the comparison corresponding to the target sample was defined as correct. Colored fields and line orientations were employed as sample stimuli in Experiment 1, and samples of food and no food and of number of pecks were employed in Experiment 2. Interference was found to be equally robust regardless of whether the interfering and target samples were each selected from any of the four dimensions (color, line orientation, food/no food, or number of pecks). Amount of interference was found to be independent of whether the interfering and target samples employed on a trial were selected from the same dimension or from different dimensions. Evidence was also obtained suggesting that line orientation comparison stimuli are more likely to elicit a response not based on memory than are color comparison stimuli.     

SPELLING AND EMERGENT PICTURE-PRINTED WORD RELATIONS ESTABLISHED WITH DELAYED IDENTITY MATCHING TO COMPLEX SAMPLES

Students with academic deficits learned delayed matching-to-sample tasks that used complex sample stimuli, each consisting of a picture and a printed word. A touch to the sample complex removed it from the computer display and produced either picture comparisons or a choice pool of letters. If the comparisons were pictures, selecting the picture identical to the preceding sample was reinforced. If the letters appeared, letter-by-letter construction of the preceding printed word sample was reinforced. The procedure engendered new constructed-response spelling performances and arbitrary relations among pictures and printed words in matching to sample. The emergence of relations among different sets of printed words (paired with the same pictures) suggested classes of equivalent stimuli. Outcome tests involving spoken words as sample stimuli suggested expansion of subjects' spelling repertoires and stimulus classes.     

Extending sequence-class membership with matching to sample

Three normal adults were first trained to point sequentially to each member of several pairs of visual stimuli. This baseline training established one class of stimuli to which subjects responded first, and another class of stimuli to which they responded second. Then, in a matching-to-sample procedure, baseline-sequence stimuli served as samples and new visual stimuli served as comparisons. Subjects were trained to choose one group of new comparisons when the sample was a "first" stimulus from the sequence baseline, and to choose the other new comparison stimuli when the sample was a "second" from the sequence baseline. When the new stimuli were then presented as pairs in the posttest, two subjects pointed to them in sequences predictable on the basis of the stimulus-class membership established during matching to sample. The failure of one subject to demonstrate sequential transfer was shown to be a consequence of the failure of the matching-to-sample procedure to establish stimulus classes. The production of sequences that were not directly trained suggested an empirical approach to the analysis of simple grammatical behavior.     

The formation of a generalized categorization repertoire: effect of training with multiple domains,samples, and comparisons

The present experiment explored the effects of three variables on the spontaneous categorization of stimuli in perceptually distinct and novel domains. Each of six stimulus domains was created by morphing two images that were the domain endpoints. The endpoints of the domains were male and female faces, two abstract drawings, a car and a truck, two banded-elevation satellite land images, a tree and a cat, and two false-color satellite images. The stimulus variants at each end of a domain defined two potential perceptual classes. Training was conducted in a matching-to-sample format and used stimuli from one or two domains, one or three variants per class as samples, and one or three variants per class as comparisons. The spontaneous categorization of stimuli in the untrained stimulus domains showed the emergence of a generalized categorization repertoire. The proportion of spontaneously categorized stimuli in the new domains was positively related to the number of domains and samples used in training, and was inversely related to the number of comparisons used in training. Differential reaction times demonstrated the discriminability of the stimuli in the emergent classes. This study is among the first to provide an empirical basis for a behavior-analytic model of the development of generalized categorization repertoires in natural settings.     

Short-term memory for responses: the "choose-small" effect

Pigeons' short-term memory for fixed-ratio requirements was assessed using a delayed symbolic matching-to-sample procedure. Different choices were reinforced after fixed-ratio 10 and fixed-ratio 40 requirements, and delays of 0, 5, or 20 s were sometimes placed between sample ratios and choice. All birds made disproportionate numbers of responses to the small-ratio choice alternative when delays were interposed between ratios and choice, and this bias increased as a function of delay. Preference for the small fixed-ratio alternative was also observed on "no-sample" trials, during which the choice alternatives were presented without a prior sample ratio. This "choose-small" bias is analogous to results obtained by Spetch and Wilkie (1983) with event duration as the discriminative stimulus. The choose-small bias was attenuated when the houselight was turned on during delays, but overall accuracy was not influenced systematically by the houselight manipulation.     

Reinforcer efficacy in a delayed matching-to-sample task.

Five domestic hens were exposed to a delayed matching-to-sample task. Conditions 1, 5, and 8 were variable-delay conditions in which five delays (0.25, 1, 2, 4, and 8 s) from the red or green sample to the presentation of the red and green comparison stimuli were presented a number of times during each session. In the fixed-delay condition (Condition 3), each delay was presented for 15 sessions under a Latin square design across birds. When improvements in accuracy across the variable-delay conditions are taken into account, the data were similar under both the variable and fixed delays. In Conditions 2, 4, 6, and 7 sample-reinforcer intervals were held at 8, 8, 4, and 2 s, respectively, while sample-choice intervals were varied within these during each session. With increasing sample-reinforcer interval, both initial discriminability (i.e., with sample-choice delay = 0) and rate of decrement in discriminability decreased. Although the former would be predicted if accuracy depends of the average sample-reinforcer interval, the latter would not. These data show that increasing the sample-choice interval had less effect on matching accuracy than increasing the sample-reinforcer interval did.     

A computational technique for improving estimates of discriminability and bias across multiple dimensions of choice

Brown and White (2009) proposed measures of discriminability and bias that accommodate additional dimensions of choice—and hence, bias—in conditional discriminations such as matching-to-sample and the yes-no signal detection task. Their proposed measures increase the statistical independence of discriminability and bias estimates, thus improving their accuracy. Because Brown and White’s (2009) equations partition response data more than do standard equations, however, their measures have a slightly lower ceiling. Consequently, measurements can be less accurate when there are few trials and discriminability and bias are extreme. We introduce a computational estimation technique that overcomes this limitation. It estimates Brown and White’s (2009) discriminability and bias measurements from an array of related measures that have a higher ceiling. Simulations show that resulting estimates of discriminability and bias are either comparable to or more accurate than measurements calculated from traditional equations or Brown and White’s (2009) direct measures, even with few trials. A worked example of our technique may be downloaded from brm.psychonomic-journals.org/ content/supplemental.     

Dimensional dominance and stimulus discriminability.

The relationship between the discriminability of scaling stimuli and assessed dimensional dominance was investigated in three studies. Sixty kindergarten children were assessed using a psychophysical scaling method to determine JND values for the size, brightness, and orientation dimensions. Thirty of the same subjects were then assessed for dimensional dominance using stimuli of two levels of known discriminability, based on the obtained JND values. In a third experiment, the remaining 30 subjects were assessed for dimensional dominance using stimuli that systematically emphasized the values of one dimension relative to the other two dimensions, again based on obtained JND values.The results indicated that (1) kindergarten children were able to perform consistently during psychophysical scaling, and there was little variability between children in their judgments of stimuli, (2) the overall level of discriminability affects dimensional dominance scaling behavior, with subjects more likely to exhibit dominance for one dimension when all the values of scaling stimuli are high in discriminability, and (3) some support for the hypothesis that dimensional dominance scaling behavior can be manipulated by manipulating the relative discriminability of scaling stimuli was found, though the trend was not clear.The relative discriminability of scaling stimuli appears to have some effects on dimensional dominance scaling behavior of young children. However, some pre-experimental bias to attend to a particular dimension seems to remain even when the values of all dimensions present are of equal and known discriminability. Dimensional dominance is a function of an interaction between discriminability of scaling stimuli and the experiential bias or perceptual set of the subject.     

Post-choice information processing by pigeons

In a conditional discrimination (matching-to-sample), a sample is followed by two comparison stimuli, one of which is correct, depending on the sample. Evidence from previous research suggests that if the stimulus display is maintained following an incorrect response (the so-called penalty-time procedure), acquisition by pigeons is facilitated. The present research tested the hypothesis that the penalty-time procedure allows the pigeons to review and learn from the maintained stimulus display following an incorrect choice. It did so by including a penalty-time group for which, following an incorrect choice, the sample changed to match the incorrect comparison, thus providing the pigeons with post-choice misinformation. This misinformation group acquired the matching task significantly slower than the standard penalty-time group (that had no change in the sample following an error). Furthermore, acquisition of matching by a control group that received no penalty time fell midway between the other two groups, suggesting that the pigeons did not merely take more care in making choices because of the aversiveness of penalty-time. Thus, it appears that in the acquisition of matching-to-sample, when the stimulus display is maintained following an incorrect choice, the pigeons can review or acquire information from the display. This is the first time that such an effect has been reported for a nonhuman species.     

The interaction between stimulus and reinforcer control on remembering.

In a symbolic matching-to-sample task, 6 pigeons obtained food by pecking a red side key when the brighter of two white lights had been presented on the center key and by pecking a green side key when the dimmer of two white lights had been presented on the center key. Across Part 1 and Parts 6 to 10, the delay between sample-stimulus presentation and the availability of the choice keys was varied between 0 s and 25 s. Across Parts 1 to 5, the delay between the emission of a correct choice and the delivery of a reinforcer was varied between 0 s and 30 s. Although increasing both types of delay decreased stimulus discriminability, lengthening the stimulus-choice delay produced a greater decrement in choice accuracy than did lengthening the choice-reinforcer delay. Additionally, the relative reinforcer rate for correct choice was varied across both types of delay. The sensitivity of behavior to the distribution of reinforcers decreased as discriminability decreased under both procedures. These data are consistent with the view, based on the generalized matching law, that sample stimuli and reinforcers interact in their control over remembering.     

Verbal self-reports of delayed matching to sample by humans

Undergraduates participated in two experiments to develop methods for the experimental analysis of self-reports about behavior. The target behavior was the choice response in a delayed-matching-to-sample task in which monetary reinforcement was contingent upon both speed and accuracy of the choice. In Experiment 1, the temporal portion of the contingency was manipulated within each session, and the presence and absence of feedback about reinforcement was manipulated across sessions. As the time limits became stricter, target response speeds increased, but accuracy and reinforcement rates decreased. When feedback was withheld, further reductions in speed and reinforcement occurred, but only at the strictest time limit. Thus, the procedures were successful in producing systematic variation in the speed, accuracy, and reinforcement of the target behavior. Experiment 2 was designed to assess the influence of these characteristics on self-reports. In self-report conditions, each target response was followed by a computer-generated query: “Did you earn points?” The subject reported by pressing “Yes” or “No” buttons, with the sole consequence of advancing the session. In some cases, feedback about reinforcement of the target response followed the reports; in other cases it was withheld. Self-reports were less accurate when the target responses occurred under greater time pressure. When feedback was withheld, the speed of the target response influenced reports, in that the probability of a “Yes” report increased directly with the speed of accurate target responses. In addition, imposing the self-report procedure disrupted target performance by reducing response speeds at the strictest time limit. These results allow investigation of issues in both behavioral and cognitive psychology. More important, the overall order in the data suggests promise for the experimental analysis of self-reports by human subjects.