Response latency,confidence, and ROCs in auditory signal detection

Response latencies were obtained from 10 Ss in auditory signal-detection experiments. The response latencies were inversely related to certainty that a signal was (or was not) presented. The S’s decision criterion was found to have an influence on response latency, which was consistent with the hypothesis that stimuli close to the current criterion elicit longer response latencies than stimuli more distant from the criterion. Comparisons among receiver operating characteristics derived from binary decisions, from the latencies of binary decisions, and from confidence ratings show that response latencies and binary decisions together yield more information about the stimulus than does the binary decision alone. However, the increment in information gained from the measurement of response latencies is in general (though not for every S) smaller than that gained by shifting from yes-no responses to a confidence-rating procedure.     

Extraretinal feedback and visual localization

The effect of saccades on visual localization was tested before, during, and after the eye movements. After saccades, localization errors were much less than the distance that the eyes had moved. It is argued that these results demonstrate that extraretinal feedback affects visual localization. The results also suggest that the feedback is related to acceleration rather than to position. Implications for inflow and outflow theories are discussed.     

Some differences among figural aftereffects,apparent motion,and paracontrast*

It has been suggested that figural aftereffects, apparent motion, and paracontrast may be produced by very similar or equivalent processes. The empirical functions relating figural aftereffect to the duration of the inspection figure and the interfigural distance are significantly different from the corresponding apparent motion and paracontrast functions. The functions relating paracontrast to the interstimulus interval are significantly different from the corresponding figural-aftereffect and apparent-motion functions. Thus, it is unlikely that the processes underlying the three phenomena are the same. Researchers who attempt to study feature analyzers in the human visual system should consider using more than one dependent variable, since none of the three phenomena contains all of the available information. Within-Ss designs should be avoided because a strong response bias exists between figural-aftereffect and apparent-motion tasks.     

Concurrent variation of response bias and sensitivity in an operant-psychophysical test

The yes-no signal detection procedure was applied to a single-response operant paradigm in which rats discriminated between a standard auditory intensity and attenuated comparison values. The payoff matrix was symmetrical (with reinforcing brain stimulation for correct detections and brief time-out for errors), but signal probability and intensity differences were varied to generate a family of isobias and isosensitivity functions. The d’ parameter remained fairly constant across a wide range of bias levels. Isobias functions deviated from a strict matching strategy as discrimination difficulty increased, although an orderly relation was maintained between signal probability value and the degree and direction of response bias.     

Some effects of interreinforcement time upon choice

Pigeons' responses were reinforced on two identical and concurrently available chain variable-interval-schedules. Unlike the typical concurrent chains procedure, both links were operative throughout, thus producing three types of concurrency: (1) concurrent initial links; (2) concurrent initial and terminal links; (3) concurrent terminal links. Choice proportions in each of these three states suggested that the pigeons were sensitive to momentary likelihoods of reinforcement: choice proportions for a schedule were higher when the schedule had been operative for some time, resulting in a higher probability of reinforcement. The study also showed that the relative rates of responding did not match the relative rates of reinforcement in any of the three states of concurrency. Instead, the choice proportions in both the concurrent initial and in the concurrent terminal links were intermediate between the scheduled and the obtained relative rates of reinforcement, while the choice proportions for a terminal link concurrent with an initial link consistently overmatched the relative interreinforcement times (and were typically 1.00). These data indicate that an accurate characterization of choice may not be obtained by considering only the relative interreinforcement interval where one interreinforcement interval is segmented into a chain. Instead, the organism's choice for a schedule will be substantially lowered by the chaining operation.     

Inverse relation between choice and local response rate with a schedule of response-produced blackouts

Pigeons were exposed to a two-key concurrent chains schedule in which identical frequencies and distributions of food presentations generated different response rates in the terminal links. An inverse relation between local rate of response in the terminal links and relative frequency of response in the initial links was observed. The high response rate was produced in one terminal link by a second-order schedule in which responding produced brief blackouts of the response key. Responding under the same schedule in the other terminal link did not produce blackouts. Under initial training and after spatial reversal of the terminal-link schedules, two of three pigeons had lower relative frequencies of response in the initial member of the chain with the higher terminal link response rate. The third pigeon showed no change in preference at reversal.     

Two temporal parameters of food postponement

Rats were trained to press a lever under schedules of food postponement. In the absence of lever presses, food was delivered periodically (food-food interval). Responses initiated a second interval (response-food interval) that was reset by each additional response. Performance was first studied at different response-food intervals with the food-food interval fixed at 30 or 60 sec, or 10 min. Response-food intervals were examined in ascending order and then recovery was studied at shorter intervals. Finally, the food-food interval was manipulated with response-food interval fixed at 30 sec. At food-food intervals of 30 and 60 sec, responding first increased and then decreased as the response-food interval increased. At the 10-min food-food interval, responding decreased with increasing response-food interval. In general, very low rates of responding occurred when the response-food interval was 60 sec or more and when it equalled or exceeded the food-food interval. However, responding was maintained in one animal when the food-food interval was decreased from 120 to 15 sec with the response-food interval at 30 sec. Results, in terms of several dependent variables, are compared with data on shock avoidance. Effects of response-independent and response-produced food and shock are discussed.     

Probability learning as a function of momentary reinforcement probability

Pigeons were trained on a probability learning task where the overall reinforcement probability was 0.50 for each response alternative but where the momentary reinforcement probability differed and depended upon the outcome of the preceding trial. In all cases, the maximum reinforcement occurred with a “win-stay, lose-shift” response pattern. When both position and color were relevant cues, the optimal response pattern was learned when the reinforcement probability for repeating the just-reinforced response was 0.80 but not when the probability was 0.65. When only color was relevant, learning occurred much more slowly, and only for subjects trained on large fixed ratio requirements.