Habituation under stress: shocked mice show nonassociative learning in a T-maze

Conflicting predictions of reinforcement and neophobia-arousal theories were evaluated in a simple choice task. Four groups of C57BL/6J mice were administered daily two-trial tests in a uniform T-maze for 10 consecutive days. For three groups, the contingencies of footshock treatments were manipulated to reinforce alternation, perseveration, or both. A control group that was not administered footshock alternated, but all three groups that were stressed perseverated more and more across tests, despite the differences in reinforcement contingencies. These results are inconsistent with the predictions of reinforcement theory but consistent with the view that stressed or aroused animals are neophobic and use nonassociative learning (habituation) to distinguish between novel and familiar alternatives.     

Food priming and short-term retention in the delayed alternation task

The delayed alternation task, with rats as subjects, was used to assess the effects of a priming food reward on subsequent retention of a reinforced target location in a T maze. Subjects received a pretrial feeding, followed by a forced-choice rewarded entry into one goal box of the maze (the “cuing” run). Following a delay interval (5–60 s), the subjects were allowed to choose either goal, with reward available only in the one not entered on the cuing run. Priming significantly reduced such alternation after 30- and 60-s delays (Experiment 1), whereas administering the reward following the cuing run had no effect on choice behavior (Experiment 2). In the third study, prefeeding had a decremental effect when the following cuing run was reinforced, but no decrement occurred when reinforcement was omitted on the cuing run. The results suggest that food reward enhances retention of spatial information, but priming reduces this effect.     

The effect of combined arousal states on attitude change

An experiment was devised in which subjects either were given a choice or were given no choice to listen to a counter-attitudinal communication. For half the subjects (Interrupt condition) the tape of the communication broke during the concluding sentence of the speech. The other half of the subjects (No Interrupt condition) heard the speech in its entirety. A recall measure indicated that subjects in the Interrupt condition recalled significantly more arguments made in the communication than subjects who heard the complete speech. This was interpreted as being a Zeigarnik effect caused by arousal created by the interruption. The choice manipulation should have created dissonance and motivated attitude change. Consistent with dissonance theory, measures of attitude change showed that greater attitude change toward the position of the speech occurred in the Choice condition than in the No Choice condition. In addition, an interaction in which significantly greater change occurred in the Choice-Interrupt condition than any of the other conditions was obtained. Since both the choice and interruption manipulations were hypothesized to be arousing, it was speculated that, in the Choice-Interrupt condition, the arousal created by the cognitive inconsistency and by the interrupted task may have combined to yield the increased attitude change. The conditions under which arousal states might combine were discussed.     

The reinforcing properties of aggressive vs nonaggressive social interactions in isolated male ICR mice (Mus musculus)

Isolated male ICR mice in a T-maze consistently selected the goal box which enabled them to fight another mouse if the alternative goal box allowed no social interaction (Experiment 1). However, if the alternative choice enabled the isolated mice to interact with another mouse through a mesh screen which prevented fighting, the preference for the opportunity to fight did not appear (Experiment 2). Because the visual, olfactory, and auditory stimuli available through the screen appeared to be as attractive as the stimuli provided by the additional opportunity to fight, it is not necessary to conclude that the stimuli reinforcing the choice behavior in Experiment 1 were provided by fighting. Since there is no compelling reason to conclude that fighting is a primary reinforcer for these isolated mice, it is not necessary to argue that the high incidence of isolation-induced fighting is the reflection of a primary aggressive motive.     

Frustation and learned helplessness.

This article reports the transfer of learned helplessness from one aversive motivator, shock to another, frustration. In experiment 1, animals were trained to approach food in a runway and concomitantly exposed to either escapable, inescapable, or no shock in a different situation. Extinction was conducted in the runway, and subsequently the animals were tested for hurdle-jump escape from the frustrating goal box. Inescapably shocked rats failed to learn to hurdle-jump, whereas escapably or nonshocked animals learned the frustration escape response. Experiment 2 replicated the basic finidngs of Experiment 1 and showed transfer of learned helplessness from shock to frustration when no running response had been first acquired in the runway.     

Acquisition and transfer effects of cued and noncued double alternation schedules with rats

In an attempt to establish patterning, rats were administered eight daily runway trials in a double alternation schedule with distinctive goal events in either a consistent or a varied sequence. Different magnitudes of reward differentiated the reinforced trials, whereas different lengths of confinement in the empty goal box distinguished the nonreinforced trials. During acquisition, rats given the consistent cue sequence “patterned”, whereas the group presented varied cues did not. Subsequently, the Consistent and Varied Cue Groups were subdivided and were administered for 2 days only one of the four acquisition training goal events. During the final 5 days of transfer testing, all subgroups were switched to receiving four daily trials with a second and then a third goal event. In agreement with expectations derived from stimulus aftereffects theory, performance was immediately in accord with the reinforcement contingencies previously established during acquisition training and not the goal event actually presented during testing.     

Can an agent's false belief be corrected by an appropriate communication? Psychological reasoning in 18-month-old infants

Do 18-month-olds understand that an agent's false belief can be corrected by an appropriate, though not an inappropriate, communication? In Experiment 1, infants watched a series of events involving two agents, a ball, and two containers: a box and a cup. To start, agent1 played with the ball and then hid it in the box, while agent2 looked on. Next, in agent1's absence, agent2 moved the ball from the box to the cup. When agent1 returned, agent2 told her "The ball is in the cup!" (informative-intervention condition) or "I like the cup!" (uninformative-intervention condition). During test, agent1 reached for either the box (box event) or the cup (cup event). In the informative-intervention condition, infants who saw the box event looked reliably longer than those who saw the cup event; in the uninformative-intervention condition, the reverse pattern was found. These results suggest that infants expected agent1's false belief about the ball's location to be corrected when she was told "The ball is in the cup!", but not "I like the cup!". In Experiment 2, agent2 simply pointed to the ball's new location, and infants again expected agent1's false belief to be corrected. These and control results provide additional evidence that infants in the second year of life can attribute false beliefs to agents. In addition, the results suggest that by 18 months of age infants expect agents' false beliefs to be corrected by relevant communications involving words or gestures.     

CHEMICAL TRANSFER OF ALTERNATION TRAINING IN THE SKINNER BOX

F jerdingstad , E. J. Chemical transfer of alternation training in the Skinner box. Scand. J. Psychol ., 1969, 10 , 220–224.—In six individual experiments one group of recipient mice was injected with brain extract from rat donors trained to alternate between bars in a Skinner box; another group was injected with extract from donors reinforced for pressing either bar irrespective of choice. During testing the recipients of 'alternation extract' showed a significantly higher tendency to alternate.     

Experiments on neophobia in wild and laboratory rats: a reevaluation.

Two experiments using food-container avoidance as an index of neophobia are reported for two strains of laboratory and one strain of wild rats. In Experiment 1 rats were fed from a single familiar container until their consumption had stabilized. Upon replacing the familiar container with a novel container, the latency of all three strains to begin feeding increased. In Experiment 2 rats were offered a choice between a familiar and a novel container containing identical food. Though there was considerable individual variation among the three strains, the wild strain was more reluctant to eat from the novel container than a hooded laboratory strain, which, in turn, was nore reluctant than an albino laboratory strain. Nonetheless, all three strains showed an initial avoidance of the novel container. It was concluded that both wild and laboratory strains are neophobic and that strain differences are ones of degree, not of kind.     

情绪对联合行动中共同表征能力的影响机制

采用联合Simon任务通过3个实验探究不同情绪维度对联合任务中共同表征能力的影响机制。实验1a、1b分别考察在高、低唤醒度条件下不同效价对个体共同表征能力的影响; 实验2在此基础上进一步探索动机维度在其中的作用。结果发现：无论效价高低, 高唤醒度都是提高个体共同表征能力的关键因素, 且动机强度在其中起一定调节作用; 而在低唤醒度条件下, 高效价会起一定补偿作用。上述结果很好地支持了参照编码假说, 也澄清了情绪不同维度对联合动作表征的影响机制。     

ON THE RELATIVE REINFORCING EFFECTS OF CHOICE AND DIFFERENTIAL CONSEQUENCES

Research on the reinforcing effects of providing choice-making opportunities to individuals with developmental disabilities (i.e., allowing them to choose reinforcers or tasks) has produced inconsistent results, perhaps because the mechanisms underlying such effects remain unclear. Choice may produce a reinforcement effect because it is correlated with differential consequences (i.e., choice may increase one's access to higher preference stimuli), or it may have reinforcement value independent of (or in addition to) the chosen stimulus. In Experiment 1, we used a concurrent-operants arrangement to assess preference for a choice condition (in which participants selected one of two available reinforcers) relative to a no-choice condition (in which the therapist selected the same reinforcers on a yoked schedule). All 3 participants preferred the choice option. In Experiment 2, we altered the schedules so that the participant selected one of two lower preference reinforcers in the choice condition, whereas the therapist selected a higher preference stimulus for the participant either half or all of the time in the no-choice condition. Participants typically allowed the therapist to select reinforcers for them (i.e., they allocated responding to the no-choice condition) when it resulted in greater access to higher preference stimuli.     

Musical preferences during and after relaxation and exercise

Effects of the listening context on responses to music largely have been neglected despite the prevalence of music listening in our everyday lives. This article reports 2 studies in which participants chose music of high or low arousal potential during (Experiment 1) or immediately after (Experiment 2) exercise or relaxation. In Experiment 1, participants preferred appropriate arousal-polarizing music over arousal-moderating music. In Experiment 2, participants preferred arousal-moderating music over arousal-polarizing music, such that their listening times contrasted clearly with those in the first study even though the same music and methods were used. Thus musical preferences interact with the listening situation, and participants' music selections represent an attempt to optimize their responses to that situation. When motivated to maintain a state of polarized arousal, listeners use music to achieve this; when they have no such goal, they use music to moderate arousal.     

Inferences about the location of food in capuchin monkeys (Cebus apella) in two sensory modalities

The authors tested the ability of capuchin monkeys (Cebus apella) to make inferences about hidden food. In Experiment 1, we showed the content of 2 boxes, 1 of which was baited (visual condition, VC) or we shook both boxes producing noise from the baited box (auditory condition, AC). Seven subjects (out of 8) were above chance in the VC, whereas only 1 was above chance in AC. During treatment, by manipulating empty and filled objects subjects experienced the relation between noise and content. When tested again, 7 capuchins were above chance in the VC and 3 in AC. In Experiment 2, we gave visual or auditory information only about the empty box and, consequently, successful choice implied inferential reasoning. All subjects (out of 4) were above chance in the VC, and 2 in the AC. Control tests ruled out the possibility that success resulted from simply avoiding the shaken noiseless box, or from the use of arbitrary auditory information. Similar to apes (Call, 2004), capuchins were capable of inferential reasoning.     

The role of exploration in win-shift and win-stay performance on a radial maze

Win-shift spatial memory tasks in a radial maze reinforce animals for avoiding previously visited rewarded arms; win-stay tasks reinforce them for returning to those arms. Win-shift tasks have generally been found much easier to perform, and this may be explained either in terms of foraging models which postulate avoidance of locations where food has been found, or in terms of the predominance of spontaneous alternation (exploration). Experiment 1 examined spontaneous alternation behavior in the radial maze as a function of whether the first visit to an arm had been rewarded or not, and showed that alternation was more probable after nonreward than after reward in both hungry and thirsty rats (a result which conflicts with the foraging account of the win-shift superiority). Experiment 2 replicated the finding that win-stay discrimination performance was inferior to win-shift. A manipulation (lengthening the delay between initial and test choices) which weakens spontaneous alternation, reduced, but did not reverse, the win-shift superiority. In Experiment 3, in order to eliminate the influence of spontaneous alternation, versions of the win-stay and win-shift tasks were devised in which, unlike the original task, all arms were familiar at the choice trial. Under those conditions win-stay was performed better than win-shift. It is concluded that spontaneous alternation plays a major role in many spatial memory tasks, and that the results can best be accounted for by combining principles of exploration and simple associative learning, without recourse to foraging models.     

Physiological arousal, dissonance, and attitude change: evidence for a dissonance-arousal link and a "don't remind me" effect

Two experiments replicated and extended research by Croyle and Cooper (1983) indicating that cognitive dissonance involves physiological arousal. In Experiment 1, subjects wrote counterattitudinal essays under conditions of high or low choice, and, to assess arousal effects owing to effort, with or without a list of arguments provided by the experimenter. In high-choice conditions only, and regardless of effort, subjects showed both arousal (heightened galvanic skin response) and attitude change. Arousal, however, did not decline following attitude change. The more effortful task (no arguments provided) produced increased arousal but not greater attitude change. In Experiment 2, the opportunity to change one's attitude following a freely chosen counterattitudinal essay was manipulated. As in Experiment 1, arousal increased following the essay but did not decline following a postessay attitude change opportunity. When subjects were not given an attitude change opportunity, however, arousal did decline. Thus, dissonance seems to create arousal, but attitude change sustains rather than reduces the arousal. It is suggested that if dissonance is a drive state, drive reduction typically may be accomplished through gradual cognitive change or forgetting.     

Gastric ulceration and adrenocortical activity after inescapable and escapable pre-shock in rats

Two experiments are reported which investigated the effects of pre-shock treatment in rats on adrenocortical activity and susceptibility to later restraint-induced ulceration. In Experiment I, animals were exposed to a single inescapable 3 minute shock on 5 consecutive days. These shocked animals exhibited sensitisation of the adrenocortical response over days, increased adrenocortical reactivity to open field testing one week later and a trend for more severe ulceration after 20 hours of restraint. In Experiment II, animals were given 20 escapable or yoked pre-shock trials on 5 consecutive days. No sensitisation of the adrenocortical response was observed. Escape animals however were found to exhibit less gastric ulceration and a reduced adrenocortical responses after 20 hours of restraint 9 days after the last preshock session.     

Rats' sensitivity to their direction of movement and spontaneous alternation behaviour

The response of rats to their prior direction of movement was examined in three spontaneous alternation experiments. In the first, a straight alley run interpolated between two T-maze trials increased goal arm alternation when it was in the same direction as that of the animal's first T-maze goal arm entry and decreased the alternation tendency when it was in the opposite direction. Experiment II found that multiple runs in one direction in a straight alley increased the likelihood that rats would subsequently enter the goal arm of a T-maze which permitted movement in an opposite direction. In the third experiment, rats entered those goal arms of an eight-arm radial maze which permitted movement in any direction which was different from that during a preceding straight alley trial. The results of these experiments indicate that rats are quite sensitive to their direction of movement and use it as a cue in guiding their behaviour in a variety of experimental situations.     

Signal modality and choice between signaled and unsignaled food

Choice between signaled and unsignaled response-independent food schedules was assessed in three experiments using a commitment procedure. In Experiment 1, subjects tested with a 5-s visual signal consistently changed from the signaled to the unsignaled schedule. Changing from the unsignaled to the signaled schedule was observed only occasionally and only at low levels. The same outcome was observed in Experiment 2 with different types of visual signals and with different stimulus combinations identifying the signal period, the signal-absent period, and the unsignaled schedule. In Experiment 3 the visual signal was replaced with an auditory signal for four of the subjects tested in Experiment 2. The subjects then changed from the unsignaled to the signaled schedule or showed a substantial reduction in choice for the unsignaled schedule. The data were assessed using a conditioned-reinforcement interpretation of choice.     

Learning to find the opponent: an ethological analysis of the behavior of paradise fish (Macropodus opercularis) in intra- and interspecific encounters.

In Experiment 1, 15 behavior patterns of male paradise fish (Macropodus opercularis; n = 72) toward a male conspecific, a male of another species, or no stimulus were recorded, both in home and novel situations. In Experiment 2, the same behaviors were recorded in a runway, and the same stimuli were used as reinforcers in the goal box (n = 18). A typical learning curve was seen when the subject found a male paradise fish in the goal box, learning was followed by apparent extinction when another species was found in the goal box, and few signs of learning were seen when the goal box was empty. Performance of the fish in both experiments can be accounted for by a strong aggressive motivation, a less strong but clear general curiosity, and habituation to the experimental procedure. In contrast to recent assertions in the literature, we conclude that aggressive behavior clearly can serve as a reinforcer in an instrumental learning situation.     

Sodium amylobarbitone and responses to nonreward

Three experiments are reported testing two alternative hypotheses concerning the behavioural effects of sodium amylobarbitone (SA): (1) that it blocks the after-effect of nonreward; (2) that it blocks conditioned frustration, elicited by stimuli associated with nonreward. In support of (2) Experiment I showed that SA given in acquisition abolished the partial reinforcement extinction effect (PREE) when rats were run at one trial a day in an alley for food reward on a continuous (CRF) or partial (PRF) reinforcement schedule. Experiment II showed that, in the goal section, the effect of the drug on the PREE was due to its presence during acquisition and was not due to state dependency; but the effect of the drug in the start section was consistent with state dependency of the PREE. In Experiment III, in opposition to (1) and again in support of (2), SA given to rats trained to show patterned running for water reward on a single alternation schedule blocked patterning by increasing running speeds on nonreward trials, not by decreasing running speeds on rewarded trials.