Sexual freedoms

Women—still—experience different forms of sexism in their daily lives. After the sixteenth‐century Protestant proclamation of the blessings of motherhood and women's bodies, and the women's sexual liberation movement of the 1960s, women's real freedoms and rights with their bodies, including sexual relations and procreation, are still being negotiated. Violence against women's bodies, including sex trafficking, relates to both the lack of appropriate education and fundamentally distorted views of humanity. Considering Luther's teaching on women as imago Dei, and attending theologically to the issues pertaining to misogyny—such as reforming the traditionally male‐centered God‐language and challenging the culture's implicit permission for ongoing violence against women—are some of the concrete steps that can be taken. Given the revelations with the #MeToo movement, the ELCA's 2018 draft on the Social Statement on Gender and Justice is timely.     

The effects of delayed reinforcement on free-operant responding

In previous studies of delayed reinforcement, response rate has been found to vary inversely with the response-reinforcer interval. However, in all of these studies the independent variable, response-reinforcer time, was confounded with the number of reinforcers presented in a fixed period of time (reinforcer frequency). In the present study, the frequency of available reinforcers was held constant, while temporal separation between response and reinforcer was independently manipulated. A repeating time cycle, T, was divided into two alternating time periods, t^D and t^Δ. The first response in t^D was reinforced at the end of the prevailing T cycle and extinction prevailed in t^Δ. Two placements for t^D were defined, an early t^D placement in which t^D precedes t^Δ and a late t^D placement in which t^D follows t^Δ. The duration of the early and late t^D was systematically decreased from 30 seconds (i.e., t^D = T) to 0.1 second. Manipulation of t^D placement and duration controlled the temporal separation between response and reinforcement, but it did not affect the frequency of programmed reinforcers, which was 1/T. The results show that early and late t^D placements of equal duration have similar overall effects upon response rate, reinforcer frequency, responses per reinforcer, and obtained response-reinforcer temporal separation. A stepwise regression analysis using log response rate as the dependent variable showed that the obtained delay was a significant first-step variable for six of eight subjects, with obtained reinforcer frequency significant for the remaining two subjects.     

Adventitious reinforcement in free-operant discrimination

The discriminative performance of rats trained under conditions in which their responses to S? postponed the appearance of S+, both for themselves and for yoked-control animals, was found to be superior to the performance of the controls in two rather different experiments. The results demonstrate the pervasiveness of adventitious reinforcement in free-operant discrimination.     

The free-operant partial reinforcement effect: A discrimination analysis

Twelve continuously reinforced rats were extinguished in a modified operant chamber, with an S^D for goal-approach after each bar-press. Three groups of twelve rats each trained under FR 10 were extinguished with the S^D for goal-approach after every 6, 10, or 14-bar-presses, respectively. Results showed: (1) number of bar-presses to extinction was a direct function of the bar-press to S^D ratio during extinction, (2) number of food or goal-approaches was independent of both training and extinction conditions, and (3) prior to the breakdown in discrimination a revised response-unit hypothesis, based on a discrimination analysis of the effect of intermittent reinforcement, accurately predicted the number of bar-presses for each FR group.     

Lever holding under free-operant avoidance

Rate of response under a free-operant avoidance procedure decreases as the response-shock interval increases. The present experiment demonstrated an inverse relation between rate of response and lever-holding time. An invariance was found in the total time per session that a subject was in contact with the lever. It is suggested that lever-holding behavior may be as sensitive as response rate to changes in the response-shock interval.     

Conditioned suppression of free-operant avoidance

The responses of white rats were maintained on an unsignalled free-operant avoidance schedule. Superimposed on the avoidance schedule was a blinking white light followed immediately by response-independent electric shock. Duration of the light stimulus was either 1 or 3 min. Avoidable shock was 1.5 mA; response-independent shock was 7.5 mA. Suppression of responding during the light stimulus (both durations) developed over sessions. Responding immediately following the response-independent light-shock sequence was neither suppressed nor accelerated. The similarity is noted between the present result and findings of “positive conditioned suppression”.     

Punishment contras during free-operant avoidance

Punishment of bar-pressing responses of rhesus monkeys with electric shock in one component of a multiple free-operant avoidance schedule suppressed responding in that component. These decreases were concomitant with response rate increases in the unpunished component (punishment contrast). Response rates in both components increased when punishment was removed and decreased in successive sessions. These effects of punishment on unpunished responding were similar to those obtained during single and multiple schedules of positive reinforcement and they suggest a further similarity in the development of discriminations during positive and negative reinforcement schedules.     

The effect of punishment on free-operant choice behavior in humans

During Phase I, three female human subjects pressed a button for monetary reinforcement in five variable-interval schedules specifying different frequencies of reinforcement. On alternate days, responding was also punished (by subtracting money) according to a variable-ratio 34 schedule. In the absence of punishment, response rates conformed to Herrnstein's equation for single variable-interval schedules. Punishment suppressed responding at all frequencies of reinforcement. This was reflected in a change in the values of both constants in Herrnstein's equation: the value of the theoretical maximum response-rate parameter was reduced, and the parameter describing the reinforcement frequency corresponding to the half-maximal response rate was elevated. During Phase II, the same five schedules (A) were in operation (without punishment), but in addition, a concurrent variable-interval schedule (B) of standard reinforcement frequency was introduced. On alternate days, responding in Component B was punished according to a variable-ratio 34 schedule. In the absence of punishment, absolute response rates conformed to equations proposed by Herrnstein to describe performance in concurrent schedules; the ratios of the response rates in the two components and the ratios of the times spent in the two components conformed to the Matching Law. When responding in Component B was punished, response rates in Component B were reduced and those in Component A were elevated, these changes being reflected in distortions of the matching relationship.     

Timing in free-operant and discrete-trial avoidance

A procedure (“discrete-trial” avoidance) was devised to differentiate between the two main theories of responding in Sidman's “free-operant” avoidance procedure. One theory, a version of two-factor theory, holds that responding is reinforced by the removal of a conditioned aversive stimulus. The conditioned aversive stimulus is held to be temporal, which accounts for the spaced responding, or timing, that Sidman's procedure produces. The other theory holds that the reinforcement for both responding and timing is shock-frequency reduction. The new procedure eliminated this reinforcement for timing, but retained the conditions for the formation of conditioned aversive temporal stimuli. According to one theory, the new procedure should have sustained timing as well as Sidman's, while according to the other, it should have sustained no timing. The results confirmed neither theory. Timing was found with both procedures, but unequally in degree and kind. Large variations in the precision of timing did not appear to be correlated with successful avoidance for either procedure.     

The effect of a pre-shock signal on a free-operant avoidance response

After 25 free-operant avoidance training sessions, a 1-min signal followed by a brief shock was presented on the average of once every 4 min. During the signal, the avoidance schedule was suspended (20 sessions). Response rates during the signal were markedly reduced. Shock rates during non-signalled periods increased. Fifteen additional sessions were given during which the signal was presented without shock. Response rates during signalled periods were greater than previously observed during signalled periods, indicating that signalled shock had suppressive control over a previously acquired avoidance response rate.     

Adrenocortical influences on free-operant avoidance behavior

Rats were conditioned to avoid shock on a free-operant avoidance schedule in which no exteroceptive stimulus signaled impending shock. Injections of adrenocorticotropic hormone (ACTH) or dexamethasone raised blood levels of glucocorticoids. These increases were accompanied by changes in avoidance performance: there was a higher frequency of long-duration interresponse times, a greater stability among them, and fewer short interresponse times, total responses, and shocks.     

Compounding discriminative stimuli controlling free-operant avoidance

The performances of three rats were stabilized on a multiple schedule that maintained responding by a free-operant avoidance schedule during independent presentations of tone and light. The simultaneous absence of these stimuli signalled shock-free periods and controlled response cessation. Subsequently, test sessions were administered consisting of independent presentations of each stimulus and these stimuli compounded (tone-plus-light). During an extinction test, additive summation was observed to the compounded stimuli, i.e., more responses were emitted to the compound than to either tone or light. During a series of 28 maintenance-test sessions in which the shock schedule remained operative, the compounded stimuli produced a generally enhanced response rate and fewer pauses terminating with shock than either single stimulus condition. These results extend the generality of free-operant additive summation to responding maintained by aversive control. In addition, a comparison of the present study with previous experiments reporting additive summation of positively reinforced responding indicates that similar variables—rate and aversive differences between training stimulus conditions—should be considered in accounting for response distributions during stimulus compounding when responding is controlled by either positive or negative contingencies.     

The effect of contingency upon the appetitive conditioning of free-operant behavior

The problem of maintaining independence between response rates and reinforcement probabilities when determining the effect of varying the response-reinforcement contingency upon free-operant behavior was solved by programming local reinforcement probabilities for response and no response on a second-by-second basis. Fifty-seven rats were trained to lever-press on schedules of water reinforcement involving different values of contingency. All rats were first trained on a high positive contingency and then shifted to less positive, zero, or negative contingencies. Under these conditions, rate of lever-pressing declined appropriately when the contingency between response and reinforcement decreased or was made negative. The decline in rate produced by a zero contingency cannot be attributed to extinction, since the probability of reinforcement given the occurrence of a response was the same as for the positive contingency from which the shift to zero was made. That is, there was no change in the opportunity for response-reinforcement contiguity. It was concluded that the technique of programming local reinforcement probabilities offers promise for more critical examinations of the effects of contingency upon free-operant behavior.     

Lever attacking by rats during free-operant avoidance

Rats pressed a lever to avoid shock on a free-operant avoidance schedule. Some subjects were also exposed to extinction in which the response-shock contingency was eliminated while the shock-shock contingency remained in effect. A specially constructed lever was used that registered not only presses, but also biting attacks on the lever. Throughout various phases of the study, shocks often elicited lever biting as well as post-shock responding. The results suggested that shock-elicited attacks that are forceful enough to activate the operandum might account for some of the responding that occurs in experiments on free-operant avoidance behavior. In particular, shock-elicited operandum attacking might account for post-shock response bursting during free-operant avoidance and the extreme persistence of responding sometimes noted when shocks are delivered during the extinction of avoidance behavior. To the extent that this is true, these phenomena should not be characterized as operant behavior in interpreting the results of experiments on free operant avoidance.     

Effects of sleep deprivation on free-operant avoidance

Two studies examined effects of sleep deprivation on free-operant avoidance by rats. In Experiment 1, a 5-s shock-shock (SS) interval and 20-s response-shock (RS) interval produced baseline performances, which were reestablished after each experimental manipulation. Once baselines were established, animals were exposed to 24, 48, or 96 hr of sleep deprivation and equivalent periods of home cage and food restriction as a control condition. Compared to baseline, sleep deprivation increased response rates by increasing the proportion of brief interresponse times (IRTs); response rates changed little in the control conditions. Percentage of shocks avoided did not systematically change across conditions. In Experiment 2, the RS interval was manipulated (10, 20, and 40 s), while the SS interval (5 s) and level of sleep deprivation (48 hr) were held constant. Across RS intervals, sleep deprivation increased response rates via a shift toward brief IRTs. In addition, sleep deprivation increased the percentage of shocks avoided as an inverse function of RS intervals.     

Generalization of free-operant avoidance behavior in pigeons

Three groups of four pigeons, trained to press a treadle on a free-operant avoidance schedule, were given auditory discrimination training. Alternating 2-min components of avoidance and no shock were paired with either a tone or white noise. The pigeons were subsequently given two types of generalization tests, with and without avoidable shocks scheduled. Two of the groups, trained interdimensionally, produced excitatory and inhibitory generalization gradients along the tone frequency dimension. A predicted post-discrimination gradient was computed from the algebraic summation of these gradients of excitation and inhibition. The predicted gradient was compared with the actual post-discrimination gradient obtained from the third group of pigeons that had been given intradimensional discrimination training on the tone frequency dimension. The predicted postdiscrimination gradient agreed in shape with the empirical postdiscrimination gradient. The results in general support Spence's (1937) gradient interaction theory.     

Signalled and unsignalled free-operant avoidance in the pigeon

Pigeons were trained to depress a lever to avoid electric shock under free-operant avoidance schedules without a warning signal, or with a warning signal that could be terminated only by a response. Most birds in the signalled avoidance procedure terminated more than 50% of the warning signals before shock. In the unsignalled avoidance procedure, several birds formed a temporal discrimination and received relatively few shocks; other birds responded only in post-shock bursts, and received many more shocks.     

Effects of food deprivation on free-operant avoidance behavior

Lever pressing was maintained by Sidman's shock-postponement procedure and Herrnstein and Hineline's shock-frequency-reduction procedure with rats. Food deprivation to 80% and 70% of the animals' body weights on free feeding resulted in decreased response rates in both avoidance paradigms tested. Reinstatement of free-feeding conditions increased body weights and response rates and decreased shock rates. The effects of food deprivation were not dependent upon any particular avoidance parameters, or types, intensities, or durations of electric shock. These results mean that weight control is essential in long-term studies of avoidance behavior, and in studies of the effects on avoidance behavior of physiological interventions, such as hypothalamic lesions, that themselves may produce weight changes.