EFFECTS OF ALTERNATIVE REINFORCEMENT: DOES THE SOURCE MATTER?1

In a chamber with a single response key, pigeon's key pecks were reinforced with food according to a variable-interval schedule. In addition, extra reinforcements occurred concurrently according to an independent schedule. In one condition, availability of the extra reinforcements was signalled by a change in key color from white to red. The extra reinforcements occurred after a peck on the red key. In a second condition, the extra reinforcements were unsignalled and occurred only after a 2-sec pause in pecking for one group of subjects and were unsignalled and occurred freely as scheduled for another group of subjects. In the first two conditions, duration of reinforcement was varied. A third condition duplicated the second but varied rate rather than duration of reinforcement. The rate of pecking varied inversely with the amount of extra reinforcement per unit time according to the same function, regardless of the condition regulating occurrence of the extra reinforcements, and regardless of whether or not a 2-sec pause was required for their occurrence. The shape of this function was predicted by Herrnstein's (1970) matching law.     

Behavioral contrast of time allocation

Pigeons' standing on a platform produced food reinforcement according to two-component multiple schedules in which either both components consisted of the same variable-interval schedule or one of these was replaced with a component without reinforcement (extinction). The components of the multiple schedule alternated every 30 sec, and were signalled by changes in the color of diffuse overhead illumination. Changing the schedule of one of the components to extinction increased the percentage of time spent on the platform during the unchanged component (behavioral contrast). This result casts doubt on accounts that attribute behavioral contrast to variations in the rate of noninstrumental elicited responses.     

Chained concurrent schedules: reinforcement as situation transition

Pigeons' pecks at two white response keys (initial-link situation) occasionally turned both keys red (terminal-link situation). When the two keys were red, pecks occasionally produced food, after which the keys were again white. In both situations, a changeover delay prevented the response-produced outcome from immediately following a change of responding from either key to the other. In the initial-link situation, the ratio of pecks at the keys closely paralleled the ratio of transitions into the terminal-link situation produced by the pecks, conforming to the well-known matching relation. In the terminal-link situation, the peck ratios deviated from the matching relation toward indifference. Overall response rate and rate of changeover were generally higher in the terminal-link situation than in the initial-link situation. The finding of matching in the initial-link situation supports a definition of reinforcement as situation transition. The differences in performance between the two situations, viewed in the light of other recent findings, suggest that the effects of a changeover delay depend on the overall reinforcing value of the choice alternatives.     

Contextual influences on phonetic identification in aphasia: the effects of speaking rate and semantic bias

Two experiments examined the influence of context on stop-consonant voicing identification in fluent and nonfluent aphasic patients and normal controls. Listeners were required to label the initial stop in a target word varying along a voice onset time (VOT) continuum as either voiced or voiceless ([b]/[p] or [d]/[t]). Target stimuli were presented in sentence contexts in which the rate of speech of the sentence context (Experiment 1) or the semantic bias of the context (Experiment 2) was manipulated. The results revealed that all subject groups were sensitive to the contextual influences, although the extent of the context effects varied somewhat across groups and across experiments. In addition, a number of patients in both the fluent and nonfluent aphasic groups could not consistently identify even endpoint stimuli, confirming phonetic categorization impairments previously shown in such individuals. Results are discussed with respect to the potential reliance by aphasic patients on higher level context to compensate for phonetic perception deficits.     

Response–reinforcer contiguity versus response-rate–reinforcer-rate covariance in rats' lever pressing: Support for a multiscale view

The multiscale molar view sees behavior as a flow, like a river, extended in time. Matching theory expresses the way activities compete for time. Relative time taken by any activity depends on relative induction. The present experiment tested matching theory applied to concurrent contingent and noncontingent food. As adjunctive activities that compete with operant activity, we recorded hopper head entries and presses on a lever near the food hopper that had no programmed consequences. Eight naïve rats were first exposed to a variable-time 60 s schedule, which across conditions was gradually transformed into a variable-interval 60 s schedule by increasing the proportion of food that was delivered contingent on pressing a lever far from the hopper. Another group of 4 rats that had been trained to press a lever near a food hopper were introduced in the second condition, in which one food delivery was contingent on far-lever pressing. We found induction following a power function to describe pressing on the far lever (operant activity). Matching theory combined with power-function induction also accounted for adjunctive activity. Results with single contingent food deliveries provided little support for the molecular view that behavior consists of discrete responses “strengthened” by immediately following reinforcers.