The effects of concurrent responding and reinforcement on behavioral output

Four birds key pecked on concurrent variable-interval one-minute variable-interval four-minute schedules with a two-second changeover delay. Response rates to the variable-interval one-minute key were then reduced by signaling its reinforcer availability and later by providing its reinforcers independently of responding. Each manipulation increased response rates to the variable-interval four-minute key even though relative reinforcement rates were unchanged. In a final phase, eliminating the variable-interval one-minute key and its schedule produced the highest rates of all to the variable-interval four-minute key. These results show that both reinforcement and response rates to one schedule influence response rates to another schedule. These results join those of Guilkey, Shull, & Brownstein (1975) in failing to replicate Catania (1963). Moreover, they violate the predictions of the equation for simple action (de Villiers & Herrnstein, 1976). In terms of a median-rate measure (reciprocal of the median interresponse time), rates to the variable-interval four-minute key were high when responding was not reduced to the variable-interval one-minute key and were low when it was reduced. This rate difference suggests a process difference between concurrent-schedule procedures that maintain high concurrent response rates versus those that do not. This process difference jeopardizes attempts to integrate single- and concurrent-operant performances within a single formulation.     

Choice and segmented interreinforcement intervals

Pigeons were trained on a two-key concurrent schedule, where food reinforcers on one key were arranged by a simple variable-interval schedule and on the other key by a chain variable-interval variable-interval schedule. When the initial link of the chain was in effect, the pigeons tended to respond more on the simple variable-interval schedule, and hence less on the chain, than would be expected from a comparison of both the local and overall rates of reinforcement of the two schedules. When the terminal link of the chain was in effect, the pigeons responded more on the chain than would be expected from a comparison of the rates of reinforcement of the schedules then in effect. Overall responding on the chain was not proportional to overall reinforcement on the chain but rather was a by-product of responding during initial- and terminal-link phases.     

Acquisition and maintenance of autoshaped key pecking as a function of food stimulus and key stimulus similarity.

The results of a number of recent studies suggest that acquisitions of autoshaped key pecking in pigeons is affected by the similarity of the grain-hopper stimulus and response-key stimulus. In Experiment 1 this hypothesis was tested by training independent groups of pigeons to key peck under six different hopper-stimulus and key-stimulus similarity conditions, and three procedures containing either immediate reinforcement, variable delay of reinforcement, or omission of reinforcement for key pecking. Number of trials to acquisition was found to be related to the similarity variable. Maintained responding was affected by the response-reinforcer contingency. This effect was found both within and between subjects. Under two of the contingencies (automaintenance and omission), maintained responding continued to be affected by the similarity of the hopper stimulus and key stimulus. In Experiment 2 pigeons were given omission training with a hopper light on or off. Both acquisition and maintenance of key pecking were facilitated by the presence of the hopper light. The present findings suggest that much of the responding reported in various automatic shaping and training procedures may reflect the effects of key stimulus/food stimulus similarity.     

Choice, relative reinforcer duration, and the changeover ratio

Relative reinforcer duration was varied in concurrent schedules with a fixed-ratio four changeover requirement. The schedule in effect after each reinforcer was randomly chosen. For all three pigeons, relative response rates overmatched relative reinforcer durations. Time allocation was less extreme and, on the average, matched relative reinforcer duration. In a subsequent manipulation, the level of preference was shown to depend on the size of the changeover requirement. These results are similar to those from related unequal reinforcement-frequency procedures.     

Autoshaped key pecking maintained by access to a social space.

When four experimentally naive pigeons were exposed to occasional forward pairings of a keylight followed by a doorlight (that signaled access to a large social space), all subjects began to peck the lit key. In a second experiment, where the keylight either preceded the presentation of the doorlight or was presented independently of it, key pecking was maintained only in the former circumstance. The unconditioned stimulus in these experiments--arrival in the social space--did not elicit pecking. Hence, the conditioned response of key pecking and the unconditioned response of entering the social space differed. This demonstration of autoshaping with a social-space unconditioned stimulus argues against a stimulus-substitution account of the findings.     

Phencyclidine discrimination in the pigeon using color tracking under second-order schedules

Pigeons were trained to track different key colors, depending on whether they had been injected with phencyclidine or saline prior to the session. A second-order schedule was used to generate large numbers of responses prior to the initial food delivery. The procedure offers several advantages over traditional procedures for studying drug discrimination.     

Stimulus control of the pigeon's ability to peck a moving target.

Two pigeons were trained to peck whichever of eight keys displayed a white field (SD). The other seven keys displayed a white "X" on a black background (S delta). Each peck to SD produced three-second access to grain, a three-second intertrial interval (ITI), and the next trial. Pecks to S delta produced a three-second timeout (TO) and the same trial. During later sessions the key displaying SD changed every t seconds (t = 3, 2, 1, .5, and .25 sec), requiring the birds to track the position of the SD. Pecks on a ninth key increased t. Several sessions employed novel stimuli to ascertain the controlling stimulus dimensions. Both birds made few errors acquiring the original discrimination. During the tracking sessions, both birds made few errors when t = .5 sec. Only one reliably lengthened t. Data from sessions with novel stimuli indicate that color and form were important aspects of SD and S delta respectively; movement contributed to the final performance.     

Mirror pecking and timeout under a multiple fixed-ratio schedule of food delivery

Pigeons were trained to peck a key under a multiple fixed-ratio 25 fixed-ratio 175 schedule of food presentation. In the first condition, either a mirror or the opportunity to produce a 30-second timeout were available. In a second condition, mirror and timeout availability were reversed for the two groups. Following a return to the initial condition, mirror and timeout keys were presented together for all birds. Mirror and timeout responses occurred predominantly in the pause in the larger fixed-ratio component, regardless of whether the opportunities for the two responses were available singly or together. Mirror responding occurred in a greater proportion of the pauses than did timeouts. When the opportunities for both mirror pecking and timeout were available concurrently, they occurred with probabilities similar to those under the single conditions. Within the pause itself, mirror responses most frequently occurred immediately after reinforcement. Timeouts occurred most frequently toward the end of the pause, and some timeouts occurred in the early part of the run. Longer preratio pausing occurred in the larger fixed-ratio component in the conditions in which the mirror was present, whether or not any mirror pecks were recorded.     

Alternative reinforcement effects on fixed-interval performance

Pigeons' key pecks were reinforced with food on a fixed-interval schedule. Food also was available at variable time periods either independently of responding or for not key pecking (a differential-reinforcement-of-other-behavior schedule). The latter condition arranged reinforcement following the first pause of t seconds after it became available according to a variable-time schedule. This schedule allowed separation of the effects of pause requirements ≤ five-seconds and reinforcement frequency. The time spent pausing increased as the duration of the pause required for reinforcement increased from 0 to 30 seconds and as the frequency of reinforcement for pausing increased from 0 to 2 reinforcers per minute. Key pecking was more evenly distributed within each fixed interval with shorter required pauses and with more frequent reinforcement for pausing. The results complement those obtained with other concurrent schedules in which the same operant response was reinforced in both components.     

Effects of d-amphetamine and pentobarbital under concurrent fixed-ratio schedules.

Pigeons were studied under a two-key concurrent fixed-ratio schedule of food presentation. During the first five sessions, the fixed-ratio requirements were 30 responses on one key (major key) and 120 responses on the other key (minor key): responding occurred almost exclusively on the major key. When the fixed-ratio requirements were then made equal at 30 responses on both keys, responding continued to predominate on the major key. The asymmetric distribution of responses persisted when the concurrent fixed-ratio fixed-ratio schedule was interrupted with periods during which the major key was associated with extinction while the other key remained associated with a fixed-ratio schedule. Additionally, in some subjects the fixed-ratio requirements were increased. These schedule modifications decreased the asymmetry in responding but did not eliminate it. d-Amphetamine decreased rates on both keys and slightly increased the asymmetric distribution of responses, while pentobarbital reversed the distribution of responses by increasing low rates and decreasing high rates. The pigeons maintained their original asymmetric distribution of responses during the 1 1/2-year-long study, despite schedule alterations and drug administrations.