A shocking grid for pigeons

Footshock is reliably delivered to pigeons standing on a surface which functions like a conventional rat grid.     

An improved respiratory system for curarized rats

A respiratory system is described in which peak expired CO₂ is continuously monitored from curarized rats. Another alteration from previous systems is that an endotracheal tube is used to minimize dead air space. The adequacy of the system was tested by maintaining curarized rats at one level of peak expired CO₂ for varying periods of time and by keeping rats at different peak expired CO₂ levels for a fixed period of time. Results of blood gas analyses indicated that values obtained with this system are similar to values in noncurarized rats, and that manipulation of expired CO₂ is an effective means of altering blood gas values.     

Some determinants of behavioral contrast in pigeons and rats

In Expt. 1, pigeons trained on a multiple variable interval, extinction schedule, showed a positive contrast effect by comparison with control groups trained with S+ only, provided that the interval between stimulus presentations was short (10 sec), but not when it was long (60 sec). Positive contrast also occurred more readily with an easier discrimination, and its appearance was highly correlated with the temporary appearance of transient contrast effects. Although a longer interval between trials produced an overall increase in rate of responding in subjects trained only with S+, it was suggested that this at best represented a different type of contrast effect. In Expt. 2, rats showed positive contrast to S+ when S− was correlated with a lower frequency of reinforcement, but not when it was correlated with a reduced magnitude of reinforcement. The results were discussed in terms of frustration theory.     

An improved method for tetrachoricr

From the ratio of the cross-products of a fourfold table, with the application of two tabled corrections, tetrachoricr's can be estimated with a mean discrepancy of less than .005 even when splits vary greatly from the medians. The necessary calculations can be handled by slide rule and the correction tables used without interpolation.     

An analysis of coordinated responding of pigeons

Experimental analyses of coordinated responding (i.e., cooperation) have been derived from a procedure described by Skinner (1962) in which reinforcers were delivered to a pair of subjects (a dyad) if both responded within a short interval, thus satisfying a coordination contingency. Although it has been suggested that this contingency enhances rates of temporally coordinated responding, limitations of past experiments have raised questions concerning this conclusion. The present experiments addressed some of these limitations by holding the schedule of reinforcement (Experiment 1: fixed ratio 1; Experiment 2; variable interval 20 s) constant across phases and between dyad members and by varying, in different conditions, the number of response keys (one to three) across which coordination could occur. Greater percentages of coordinated responding occurred under the coordinated-reinforcement phases than under independent-reinforcement phases in most conditions. The one exception during the one-key condition of Experiment 1 appeared to be a consequence of variability introduced by the independent-reinforcement phase procedure. Furthermore, coordination percentages decreased with increasing response options under both schedules. These results confirm and extend the finding that coordination contingencies control higher rates of temporally coordinated responding than independent-reinforcement contingencies do.     

Biphasic constant-current stimulator for whole-animal shocking of marine animals

A constant-current stimulator delivering biphasic pulses was designed and constructed for whole-animal shocking during aversive conditioning of Pleurobrartchaea, a marine gastropod mollusk used for behavioral and neurophysiological research. The advantages of whole-animal stimulation are discussed and results are briefly described with regard to the factors involved in evaluating the procedure. The circuit design and electrode considerations are presented in detail. The basic stimulator design has potential for use as a general instrument for behavioral and physiological research.     

Effects of pre-trial response requirements on self-control choices by rats and pigeons

Parallel experiments with rats and pigeons examined whether the size of a pre-trial ratio requirement would affect choices in a self-control situation. In different conditions, either 1 response or 40 responses were required before each trial. In the first half of each experiment, an adjusting-ratio schedule was used, in which subjects could choose a fixed-ratio schedule leading to a small reinforcer, or an adjusting-ratio schedule leading to a larger reinforcer. The size of the adjusting ratio requirement was increased and decreased over trials based on the subject's responses, in order to estimate an indifference point-a ratio at which the two alternatives were chosen about equally often. The second half of each experiment used an adjusting-delay procedure-fixed and adjusting delays to the small and large reinforcers were used instead of ratio requirements. In some conditions, particularly with the reinforcer delays, the rats had consistently longer adjusting delays with the larger pre-trial ratios, reflecting a greater tendency to choose the larger, delayed reinforcer when more responding was required to reach the choice point. No consistent effects of the pre-trial ratio were found for the pigeons in any of the conditions. These results may indicate that rats are more sensitive to the long-term reinforcement rates of the two alternatives, or they may result from a shallower temporal discounting rate for rats than for pigeons, a difference that has been observed in previous studies.     

An improved video multiplexer for behavioral research

Wellens and Revert (1979) described a solid-state circuit that allowed two sources of video information to be multiplexed and recorded using one videotape machine. On playback, the demultiplexed video signal allowed the original video channels to be viewed independently on separate television monitors. Recent changes in videocassette recorder technology have improved the playback quality of recorded images but disrupt the demultiplexing process when freeze frame or search options are selected. Improved multiplexing techniques that overcome these limitations are described.     

An improved technique for creating hemifacial chimeras

In numerous studies, facial composites of the right and left hemifaces have been used to explore lateral differences in facial expressions. In the majority of these studies, a single technique has been used to create the stimuli: “Wolff’s split half technique,” which was devised at the beginning of the century. Chimeras thus made are weakened by several confounding factors (e.g., hair form, background, shadows), which are unrelated to the original stimuli and consequently may interfere with the examination of subtle facial expressions. This paper offers a modified method using computer graphics that seems to solve such drawbacks.     

An improved algorithm for predicting free recalls

Laming [Laming, D. (2006). Predicting free recalls. Journal of Experimental Psychology: Learning, Memory, and Cognition, 32, 1146-1163] has shown that, in a free-recall experiment in which the participants rehearsed out loud, entire sequences of recalls could be predicted, to a useful degree of precision, from the prior sequences of stimuli and rehearsals. This article describes an improved predictive algorithm, which is then used to re-analyse two further sets of free-recall data. Prediction is compared, generically, with conventional modelling, represented here by three recent models of free recall that are concerned with recalls only, not with rehearsals. Some implications are drawn, from the use of rehearsal data by the predictive algorithm, for some of the constituent assumptions embodied in those three models.     

Effects of reinforcer magnitude on responding under differential-reinforcement-of-low-rate schedules of rats and pigeons

Experiment I investigated the effects of reinforcer magnitude on differential-reinforcement-of-low-rate (DRL) schedule performance in three phases. In Phase 1, two groups of rats (n = 6 and 5) responded under a DRI. 72-s schedule with reinforcer magnitudes of either 30 or 300 microl of water. After acquisition, the water amounts were reversed for each rat. In Phase 2, the effects of the same reinforcer magnitudes on DRL 18-s schedule performance were examined across conditions. In Phase 3, each rat responded unider a DR1. 18-s schedule in which the water amotnts alternated between 30 and 300 microl daily. Throughout each phase of Experiment 1, the larger reinforcer magnitude resulted in higher response rates and lower reinforcement rates. The peak of the interresponse-time distributions was at a lower value tinder the larger reinforcer magnitude. In Experiment 2, 3 pigeons responded under a DRL 20-s schedule in which reinforcer magnitude (1-s or 6-s access to grain) varied iron session to session. Higher response rates and lower reinforcement rates occurred tinder the longer hopper duration. These results demonstrate that larger reinforcer magnitudes engender less efficient DRL schedule performance in both rats and pigeons, and when reinforcer magnitude was held constant between sessions or was varied daily. The present results are consistent with previous research demonstrating a decrease in efficiency as a function of increased reinforcer magnituide tinder procedures that require a period of time without a specified response. These findings also support the claim that DRI. schedule performance is not governed solely by a timing process.     

Tests of behavior momentum in simple and multiple schedules with rats and pigeons.

Four experiments examined the relationship between rate of reinforcement and resistance to change in rats' and pigeons' responses under simple and multiple schedules of reinforcement. In Experiment 1, 28 rats responded under either simple fixed-ratio, variable-ratio, fixed-interval, or variable-interval schedules; in Experiment 2, 3 pigeons responded under simple fixed-ratio schedules. Under each schedule, rate of reinforcement varied across four successive conditions. In Experiment 3, 14 rats responded under either a multiple fixed-ratio schedule or a multiple fixed-interval schedule, each with two components that differed in rate of reinforcement. In Experiment 4, 7 pigeons responded under either a multiple fixed-ratio or a multiple fixed-interval schedule, each with three components that also differed in rate of reinforcement. Under each condition of each experiment, resistance to change was studied by measuring schedule-controlled performance under conditions with prefeeding, response-independent food during the schedule or during timeouts that separated components of the multiple schedules, and by measuring behavior under extinction. There were no consistent differences between rats and pigeons. There was no direct relationship between rates of reinforcement and resistance to change when rates of reinforcement varied across successive conditions in the simple schedules. By comparison, in the multiple schedules there was a direct relationship between rates of reinforcement and resistance to change during most tests of resistance to change. The major exception was delivering response-independent food during the schedule; this disrupted responding, but there was no direct relationship between rates of reinforcement and resistance to change in simple- or multiple-schedule contexts. The data suggest that rate of reinforcement determines resistance to change in multiple schedules, but that this relationship does not hold under simple schedules.     

An improved circuit for control of LED luminance

The light-emitting diode (LED) is becoming increasingly popular as a luminance source in behavioral research. We describe a simple, inexpensive LED driver circuit that produces luminances almost linearly proportional to an input voltage. Negative feedback provides a stable output. Unlike previous designs, the LED is ground referenced.