I like it because I said that I like it: evaluative conditioning effects can be based on stimulus-response learning

Evaluative conditioning (EC) effects are often assumed to be based on a learned mental link between the CS (conditioned stimulus) and the US (unconditioned stimulus). We demonstrate that this link is not the only one that can underlie EC effects, but that if evaluative responses are actually given during the learning phase also a direct link between the CS and an evaluative response-a CS-ER link-can be learned and lead to EC effects. In Experiment 1, CSs were paired with USs and participants were asked to evaluate the pairs during the conditioning phase. Resulting EC effects were unaffected by a later revaluation of the USs, suggesting that these EC effects can be attributed to CS-ER learning rather than to CS-US learning. Experiment 2 replicated Experiment 1 with the difference that no evaluative responses were given during the learning phase. EC effects in this study were influenced by US revaluation, suggesting that these EC effects are mainly based on CS-US learning. In Experiment 3, it was shown that EC effects can be found even if the USs are entirely removed from the procedure and the CSs are only paired with enforced evaluative responses. Together the experiments show that the valence of a stimulus can change because of a contingency with an evaluative response. (PsycINFO Database Record (c) 2011 APA, all rights reserved).     

Dependence of apparent movement of a subjective figure on the perceptual fate of inducing elements

In a series of demonstrations, two stimulus frames that contained subjective figures were alternated. It is shown that the perception of apparent movement of a subjective figure depends upon the configuration of the inducing stimuli and whether or not conditions of presentation favor the short-range or long-range process in apparent movement. Those conditions that favor the long-range process result in global apparent movement of the subjective figure. However, those conditions that favor the short-range process may prevent apparent movement of the subjective figure, or may result in a kind of apparent movement that is qualitatively different from that seen when similar physical contours are alternated. These results are interpreted in terms of the assumed differences between the short-range and long-range processes.     

Forward and backward blocking in human contingency judgement

Three experiments investigated whether a process akin to Kamin's (1969) blocking effect would occur with human contingency judgements in the context of a video game. Subjects were presented with sets of trials on each of which they could perform a particular action and observe whether the action produced a particular outcome in a situation in which there was an alternative potential cause of the outcome. In Experiment 1 it was found that prior observation of the relationship between the alternative cause and the outcome did indeed block or reduce learning about the subsequent action-outcome relationship. However, exposure to the relationship between the alternative cause and the outcome after observing the association between the action and the outcome also reduced judgements of the action-outcome contingency (backward blocking), a finding at variance with conditioning theory. In Experiment 2 it was found that, just as is the case with forward blocking, the degree of backward blocking depended on how good a predictor of the outcome the alternative cause was. Finally, in Experiment 3 it was shown that the backward blocking effect was not the result of greater forgetting about the action-outcome relationship in the experimental than in the control condition. These results cast doubt upon the applicability of contemporary theories of conditioning to human contingency judgement.     

Taste preconditioning augments odor-aversion learning

On the basis of previous work that has shown a taste can potentiate odor-aversion conditioning in AX+ conditioning, 6 experiments used rats to examine the effects of pairing a preconditioned taste (A) with a novel odor cue (X) in an A+/AX+ aversion conditioning design. Experiments 1A and 1B demonstrated that a preconditioned taste produced a robust odor aversion that was significantly stronger than a potentiated odor aversion. The results of Experiment 2 showed that the robust odor aversion produced by A+/AX+ conditioning was not the result of the potentiated odor aversion summating with generalization from the taste aversion. The augmented odor aversion was produced only when the taste and odor stimuli were presented simultaneously (Experiment 3) and the preconditioned taste aversion was intact at compound conditioning (Experiment 4). Pairing a novel odor with a preconditioned taste was not sufficient to condition an aversion to odor (Experiment 5), although other results implicated a role for an association between odor and taste in the odor augmentation effect (Experiment 6). The present results have implications for current models of taste + odor interactions in flavor-aversion conditioning.     

Backward Sensory Preconditioning When Reinforcement Is Delayed

In two experiments rats received an initial phase of training in which two neutral stimuli were presented as a serial compound (A-X). In a second phase, Awas established as a signal for a shock reinforcer, the shock being presented immediately after the termination of A (the immediate condition) or after a 5-sec interval (the trace condition). A final test phase showed that not only A but also X was capable of evoking conditioned suppression (a backward sensory preconditioning effect). The degree of suppression evoked by X was not correlated with that evoked by A. In both experiments the A trained with immediate reinforcement was more suppressive than that trained with the trace procedure, but in Experiment 1 the trace and immediate groups did not differ in the response they showed to X, and in Experiment 2 (which allowed a within-subject comparison) the trace procedure resulted in more suppression to X than did immediate conditioning of A. These results disconfirm the suggestion that the backward sensory preconditioning effect depends on the formation of an associative chain: X-A-shock. They are consistent with the proposal that the associatively activated representation of X is able to form a direct association with the reinforcer during A-shock training.     

The generation effect with homographs: Evidence for postgeneration processing

The generation effect is the phenomenon in which words are remembered better when generated than when read. These experiments test the possibility that at least one consequence of generating is enhanced semantic processing. Homographs were used as targets, presented with rhymes in Experiment 1 so as not to bias meaning, and with synonyms in Experiment 2 to bias one meaning of each homograph. In beth experiments, extralist synonym cues were provided at recall. In Experiment 1 a generation effect was obtained when the retrieval cues biased the dominant meaning of the homograph (determined from free association norms), whereas in Experiment 2 a generation effect was found when the retrieval cues biased the same meaning that was biased during study. In neither experiment was a generation effect obtained with retrieval cues that biased the other meaning of each homograph. These results indicate that the generation effect is dependent upon the compatibility of the semantic processing conducted at study and test. Since it is impossible to process the meaning of a homograph when generating it from a rhyme cue, the meaning of the homograph could only have been processed after the word had been generated. The finding in Experiment 1 that a generation effect was obtained with rhymes when semantic retrieval cues were provided demonstrates that the enhancement properties associated with generation are not restricted to the information used to guide the generation process. This finding also indicates that one locus of the generation effect is in the processing that occurs after the word has been generated.     

Mechanisms underlying retarded emergence of conditioned responding following inhibitory training: evidence for the comparator hypothesis

The comparator hypothesis posits that conditioned responding is determined by a comparison at the time of testing between the associative strengths of the conditioned stimulus (CS) and stimuli proximal to the CS at the time of conditioning. The hypothesis treats all associations as being excitatory and treats conditioned inhibition as the behavioral consequence of a CS that is less excitatory than its comparator stimuli. Conditioned lick suppression by rats was used to differentiate four possible sources of retarded responding to an inhibitory CS. These include habituation to the unconditioned stimulus (US), latent inhibition to the CS, blocking of the CS-US association by the conditioning context, and enhanced excitatory associations to the comparator stimuli. Prior research has demonstrated the first three phenomena. Therefore, we employed parameters expected to highlight the fourth one--the comparator process. In Experiment 1, our negative contingency training was shown to produce a conditioned inhibitor that passed inhibitory summation and retardation tests. In Experiment 2 we found transfer of retardation from an inhibitory CS to a novel stimulus when the location where retardation-test training occurred was excitatory, which is indicative of contextual blocking and/or comparator effects. In Experiment 3, extinction of the conditioning context was found to attenuate retardation regardless of whether extinction occurred before or after the CS-US pairings of the retardation test. This indicates that much of the present retardation was due to the comparator process rather than to contextual blocking. Experiment 4 demonstrated that habituation to the US did not contribute to retardation in the present case. Collectively, these studies suggest that retardation following inhibitory training can be explained without recourse to any of the traditional mechanisms of conditioned inhibition.     

Blocking and unblocking of conditioned analgesia

Two experiments with rat subjects assessed the blocking phenomenon using inhibition of responding to painful thermal stimulation as an index of conditioned analgesia established through conditioned stimulus (CS)-shock pairings. In Experiment 1, a group of rats receiving the standard blocking procedure ($\text{A+}\text{AB+}$) showed shorter response latencies during a hot plate test of pain sensitivity in the presence of the added CS than groups of rats receiving various blocking control procedures. Experiment 2 replicated the blocking outcome of Experiment 1 and also demonstrated that the addition of a second shock unconditioned stimulus (US) during the compound conditioning phase attenuated the blocking effect; i.e., unblocking was observed. However, the deletion of a second shock US during compound conditioning in a group that had received two shocks on each trial in the first phase of the experiment failed to result in unblocking. These data extend the associative account of conditioned analgesia to situations involving stimulus selection and the implications for the analysis of aversive learning are discussed.     

Backward and forward blocking in human electrodermal conditioning: Blocking requires an assumption of outcome additivity

Blocking was observed in two human Pavlovian conditioning studies in which colour cues signalled shock. Both forward (Experiment 1) and backward (Experiment 2) blocking was demonstrated, but only when prior verbal and written instructions suggested that if two signals of shock (A+ and B+) were presented together, a double shock would result (AB++). In this case, participants could assume that the outcome magnitude was additive. Participants given non-additivity instructions (A+ and B+ combined would result in the same outcome, a single shock) failed to show blocking. Modifications required for associative models of learning, and normative statistical accounts of causal induction, to account for the impact of additivity instructions on the blocking effect, are discussed. It is argued that the blocking shown in the present experiments resulted from the operation, not of an error-correction learning rule, nor of a simple contingency detection mechanism, but of a more complex inferential process based on propositional knowledge. Consistent with the present data, blocking is a logical outcome of an A+/AB+ design only if participants can assume that outcomes will be additive.     

Overshadowing and associability change

Three appetitive Pavlovian conditioning experiments with rats examined the associability of stimuli A and B that had a history of compound conditioning (AB+), relative to stimuli X and Y that had a history of conditioning in isolation (X+, Y+). Following this training, Experiment 1 revealed that conditioned responding was higher to X and Y than to A and B (overshadowing). In a subsequent AY+, AX-, BY- test discrimination, the AY/BY discrimination was solved more readily than the AY/AX discrimination. In Experiment 2, following AB+, X+, Y+ training, A and Y were presented as a compound and signaled the availability of reinforcement upon the performance of an instrumental response. Test trials in which A and Y were presented alone, and in extinction, revealed that A acquired greater control of instrumental responding than Y. Experiment 3 revealed that following AB+, X+, Y+ training, A and B served as more effective discriminative stimuli for instrumental responding than X and Y. Overall, these results imply that the associability of stimuli conditioned in compound is higher than stimuli conditioned in isolation. These results are discussed in terms of attentional theories of associative learning.     

The Role of Mediated Conditioning in Acquired Equivalence

In Experiment 1 rats received initial training in which delivery of a sucrose pellet was signalled by an auditory cue. This cue was then paired with shock in a second phase of training. In a test the rats showed an unwillingness to perform an instrumental response that yielded the sucrose pellet. This was interpreted as indicating that the associatively activated representation of the pellet had acquired aversive properties during the shock-reinforced stage of training. Experiment 2 replicated this mediated conditioning effect making use of a Phase 1 training procedure, modelled on that used by Honey and Hall (1989) to demonstrate acquired equivalence of cues, in which two auditory cues were each used to signal sucrose pellets. A further test revealed that this training resulted in enhanced generalization between these two cues. It was argued that this effect is mediated by the conditioned aversive properties of the common associate of the two auditory cues.     

The resistance of renewal to instructions that devalue the role of contextual cues in a conditioned suppression task with humans

The renewal of extinguished conditioned behaviour appears to reflect context-dependent learning. The present research used a conditioned suppression task with humans to examine whether instructions concerning the context could influence renewal. Pairings of a conditional stimulus (CS) and unconditional stimulus (US) were made in one context, followed by extinction trials of CS alone in a second context, and test trials of CS alone upon return to the original learning context. Four experiments tested whether the renewal of conditioned suppression observed during test would be attenuated if participants were instructed that the context changes were irrelevant to the predictive relationship between the CS and US. Using a differential conditioning design, no attenuation was found when the instructions were given prior to conditioning (Experiment 1) or immediately prior to the test trials (Experiment 2). The latter result was replicated with a single-cue conditioning design and further controls for exposure to the extinction contexts (Experiment 3). The collection of on-line ratings about the relationship between the contextual changes and the predictive nature of the CS indicated that participants did attend to and believe the instructions (Experiment 4). The results point to the resistance of renewal to explicit instructions that attempt to devalue the role of the contextual cues.     

Instrumental to Pavlovian transfer: Learning about response-reinforcer contingencies affects subsequent learning about stimulus-reinforcer contingencies

Two experiments examined the interaction between response-reinforcer (R-S) and stimulus-reinforcer (S-S) learning. In both experiments, three groups of rats were exposed to escapable, yoked inescapable, or no shocks. All groups were then exposed to either two or four sessions of truly random control (TRC) conditioning (Experiment 1) or to an excitatory conditioning procedure (Experiment 2) in which the shock US occurred with either moderate or low probability. Excitatory strength of the CS was assessed during extinction by a conditioned emotional response (CER) test. Inescapably shocked rats conditioned less than did their escapably shocked and nonshocked partners under all TRC conditions of Experiment 1, but only conditioned less than their partners in Experiment 2 when exposed to the moderate CS-US contingency for four sessions. These results provide a clear demonstration of transfer between instrumental training and Pavlovian excitatory conditioning and thus, support the influence of learning about R-S contingencies upon subsequent learning about S-S contingencies. Both a contextual blocking interpretation and an expansion of the learned helplessness theory were discussed as possible explanations of this transfer.     

Kinetic subjective contours

Continuous changes in spatially separated figures can evoke perception of subjective contours and figures in physically homogeneous space between them. This occurs when all of the interruptions in the objectively present patterns (inducing elements) can be seen as caused by a unitary figure partly occluding them. Two experiments demonstrated and explored this phenomenon. In both, displays were presented to subjects under three conditions. In one condition, stationary inducing elements were shown as they would be interrupted by a figure rotating in front of them. In another condition, the background and inducing elements rotated, with interruptions occurring as if a stationary figure were in front. In a third condition, observers were shown 10 static views taken from the figure-rotation sequence for each display. Subjects consistently perceived unitary central figures with well-defined forms and clear edges from pattern changes given by figure movement and background movement. As with static subjective figures, kinetic subjective figures appear in front of, partly occluding, the inducing elements. These percepts form rapidly, and they depend upon temporal relations rather than upon information present in momentary views. Subjects occasionally reported subjective edges or a central figure in the stationary displays in Experiment 1, but not at all in Experiment 2, in which guessing tendencies were reduced by more specific instructions. The existence of kinetic subjective contours suggests that the visual system readily utilizes relationships among occlusion events separated in space and time. The minimum conditions for contour perception require neither information all along an edge nor simultaneous specification of the edge at two or more places.     

Signalling and incentive processes in instrumental reinforcer devaluation

We have previously reported that conditioning an aversion to the reinforcer using an isotonic lithium chloride (LiCl) solution following instrumental training reduces performance in a subsequent extinction test only if animals are re-exposed to the reinforcer prior to the test. Rescorla (1992), in contrast, reported an immediate devaluation effect using a hypertonic LiCl solution that did not depend upon re-exposure. In two experiments we examined the effect of using a hypertonic LiCl solution to condition the aversion to the reinforcer on subsequent instrumental performance in extinction, with and without re-exposure. In Experiment 1 thirsty rats were trained to press a lever for a sucrose solution before being injected with 0.6 M LiCl either immediately or after a delay. Half of the immediate and delay groups were then re-exposed to the sucrose in the absence of the lever, with the remainder being exposed to water. Contrary to the previously reported effects of isotonic LiCl, a hypertonic solution induced a reinforcer devaluation effect in all the immediately poisoned animals, which did not depend upon re-exposure to the reinforcer. In Experiment 2 the possibility that this devaluation effect was induced by the discomfort associated with the hypertonicity of the solution was assessed by replicating Experiment 1 but, in addition, using two immediately poisoned groups given the LiCl injection under anaesthesia. In the absence of anaesthesia, the devaluation effect observed without re-exposure to the reinforcer in Experiment 1 was replicated. When the injection was given under anaesthesia, however, a reinforcer devaluation effect was observed only in animals that were re-exposed to the reinforcer prior to the extinction test. These results were interpreted as evidence that a reinforcer devaluation effect induced by pairing the reinforcer with illness depends upon a process of incentive learning, whereas a devaluation effect mediated by learning a signalling relationship between the reinforcer and somatic discomfort does not.     

Contralateral transfer of inhibitory and excitatory eyelid conditioning in the rabbit

In Experiment I, rabbits received training to establish a clicker as a conditioned inhibitor. In a subsequent test phase this stimulus was used as a signal for shock either to the eye reinforced during initial training or to the opposite eye. Learning to the clicker was slower in both conditions than in the appropriate control groups. The second experiment replicated the results of those subjects trained and tested with opposite eyes and ruled out the possibility that the slower learning was due to the effects of latent inhibition. Experiment III demonstrated that excitatory conditioning to a clicker to one eye facilitated future excitatory conditioning to that stimulus to the opposite eye. These results are consistent with the view that inhibitory and excitatory conditioning both involve the acquisition of a general, motivational conditioned response which is capable of mediating the transfer of conditioning across different response systems.     

Naloxone and Pavlovian fear conditioning

Previous research has shown that pretreating rats with the opiate antagonist naloxone increases the freezing that follows painful electric shock. Three experiments, using freezing behavior as a dependent variable, were carried out to determine whether the drug might cause this effect by enhancing fear conditioning. Two of the studies employed a differential context fear-conditioning paradigm. Naloxone did not affect freezing behavior during the preshock adaptation period. In Experiment 1, naloxone was found to increase resistance to extinction in the S+ context. In Experiment 2, naloxone was found to increase freezing in the S+ context. This effect was dependent upon administering naloxone during training but not dependent on administering it during testing. The third study employed a generalization paradigm. It was found that naloxone's effect on postshock freezing was dependent on the place of testing; as the contextual cues of the test chamber were changed from those of the conditioning chamber, the effect of naloxone on freezing was reduced. The results of these experiments lend strong support to the hypothesis that naloxone increases freezing by enhancing the conditioning of fear to contextual stimuli associated with shock.     

Second-order conditioning with diffuse auditory reinforcers in the pigeon

Pigeon subjects were used in five experiments investigating second-order conditioning with visual second-order and diffuse auditory first-order stimuli. Experiment 1 used a discriminative conditioning procedure to demonstrate reliable and substantial second-order conditioning with these stimuli. In Experiments 2 and 3, extinction of the auditory first-order stimulus after second-order conditioning had little effect upon responding to the second-order stimulus, when compared to a stimulus whose reinforcer was maintained. Experiment 4 compared directly the susceptibility of second-order responding to extinction of the first-order reinforcing stimulus as a function of the modality of that reinforcer. When a visual second-order stimulus was paired with a visual reinforcer, and the response to the latter was extinguished, then second-order responding was greatly reduced relative to control levels. In contrast, when that reinforcer was an auditory stimulus, second-order responding was not affected by the current value of the first-order stimulus after conditioning. Finally, in Experiment 5 the auditory stimulus was established as a reinforcer through discriminative-operant training. Following second-order conditioning, extinction of responding to this stimulus again had little impact upon responding to the second-order stimulus with which it had been paired. These results are discussed in terms of previous work on second-order conditioning with rat and pigeon subjects.     

Parallel acquisition of awareness and differential delay eyeblink conditioning

There is considerable debate about whether differential delay eyeblink conditioning can be acquired without awareness of the stimulus contingencies. Previous investigations of the relationship between differential-delay eyeblink conditioning and awareness of the stimulus contingencies have assessed awareness after the conditioning session was finished using a post-experimental questionnaire. In two experiments, the point at which contingency awareness developed during the conditioning session was estimated from a button-press measure of expectancy of the unconditioned stimulus (US). In both experiments, knowledge of the stimulus contingencies and acquisition of differential delay eyeblink conditioning developed approximately in parallel. In Experiment 1 it was shown that predicting the US facilitated eyeblink conditioning compared with predicting the eyeblink response. In Experiment 2, a masking task was used that slowed down the emergence of awareness, and it was shown that differential conditioning only occurred in participants who were able to predict the US. The current findings challenge the hypothesis that differential delay eyeblink conditioning is entirely mediated by a functionally and neurally distinct nondeclarative learning system.     

Analysis of the learned irrelevance effect in appetitive Pavlovian conditioning

In Experiments 1 and 2 rats received uncorrelated presentations of a light conditioned stimulus (CS) and a food unconditioned stimulus (US) on each day of a preexposure phase. Control subjects received the same number of USs during the first half of preexposure and the same number of CSs during the second. Uncorrelated preexposure retarded inhibitory conditioning. Experiment 3 showed, however, that the different patterns of US preexposure experienced by the two groups could in itself influence the course of subsequent inhibitory conditioning. When this factor was equated by restricting the uncorrelated treatment to the first half of the pre-exposure phase (Experiment 2) or by extending the control treatment throughout the phase (Experiment 4) it was found that uncorrelated preexposure retarded excitatory conditioning, but facilitated inhibitory conditioning. This outcome challenges an interpretation in terms of the concept of learned irrelevance, which predicts that uncorrelated preexposure should retard both forms of conditioning.