Effects of criterion-level probing on demonstrating newly acquired discriminative behavior.

The purpose of the study was to determine whether probes of the final criterion-level discrimination administered during and after training provided an accurate measure of acquisition. Training and probe stimuli were designed to make training and probe trials initially very discriminable and then progressively less discriminable as training progressed. Initially, the discrimination required on probe trials was more difficult than the discrimination required on training trials. However, this difference in difficulty was gradually eliminated as training stimuli were topographically altered and made identical to probe stimuli by the end of training. Results showed that while correct responding was maintained throughout training, error patterns occurred on all probe trials administered during training. Error patterns developed regardless of whether probe trials occurred only at the beginning of training sessions (temporally discriminable probes) or were randomly interspersed in the training sessions (temporally indiscriminable probes). Probe error patterns seemed to be controlled by the stimulus properties of training and probe trials. Thus, probes did not measure acquisition as it occurred during training. Probe error patterns were maintained when probes were administered after completion of training. This final measure of acquisition did not agree with the demonstration of acquisition provided by the final training trial. The results suggest that probe trials can measure a different stimulus-response relationship from that trained when training starts with an easier or known discrimination and probes involve a final or criterion test of a more difficult or unknown discrimination. Stimulus control of correct responses versus error patterns is discussed.     

Gerbils in space: performance on the 17-arm radial maze.

In Experiment 1 six hungry gerbils received six trials per day on a 17-arm radial maze. During each trial the subjects were allowed to choose freely among the arms, each of which contained a food pellet, until each arm had been visited once or until eight minutes had elapsed. An error was recorded when the subject entered a previously visited arm. The gerbils quickly learned not to re-enter previously visited arms and generally made errors on fewer than 15% of entries, performance comparable to that of the rat and superior to that of other species tested in the radial arm maze. The intertrial-interval duration did not affect accuracy of arm choices during acquisition but did influence asymptotic accuracy. Accuracy did not change systematically over the six trials. A high proportion of arm entries were to nearby arms. Errors occurred most often towards the end of a trial. Odor cues were not important. When the number of trials per day was reduced from six to one, accuracy deteriorated slightly. In Experiment 2 neither the transposition of extramaze cues nor the placement of the maze in a different room had large disruptive effects on accuracy. In Experiment 3 the addition of three explicit intramaze brightness cues aided accuracy, perhaps by permitting the subjects to decompose the large maze into three smaller mazes, although there was no direct evidence that this was the case. Implications of a number of these results for models of spatial maze performance were discussed.     

损毁下丘脑弓状核、中缝背核和蓝斑对大鼠应激镇痛的影响

本文用不能躲避的间歇脚底电刺激引起大鼠应激,用电刺激鼠尾-嘶叫法测定镇痛效应,研究下丘脑弓状核(脑内β-内啡肽能神经元胞体集中的部位)、中缝背核(脑内5-羟色胺能神经元胞体主要集中的部位之一)和蓝斑(脑内去甲肾上腺素能神经元胞体主要集中的部位之一)与应激镇痛的关系。 用新生大鼠腹腔注射谷氨酸-钠的方法损毁弓状核后,用海人酸和电解两种方法损毁中缝背核或蓝斑后,应激镇痛效应均明显减弱。由于谷氨酸-钠和海人酸只选择性地损毁神经元胞体,故认为脑内的β-内啡肽能神经元、5-羟色胺能神经元和去甲肾上腺素能神经元均参与应激的行为镇痛。     

Strategic factors in a lexical-decision task: Evidence for automatic and attention-driven processes

The present study examined strategic factors in a semantic-priming, lexical-decision task. The first experiment demonstrated that the greater the proportion of related word-word pairs to unrelated word-word pairs, the greater the amount of facilitation, a result which is consistent with others reported in the literature. The second experiment demonstrated that this strategic factor apparently requires that sufficient time (at least several hundred milliseconds) be available for the processing of the priming word, and thus is probably caused by attention-driven processes. The third experiment replicated and extended the results of the first two studies by demonstrating that prime-target stimulus onset asynchrony is an important limiting factor in determining whether such proportion-induced strategic factors are involved in word-recognition processes, even when no other aspect or variable of the procedure changes. The results are discussed in the context of Posner and Snyder’s (1975a) two-process model of word recognition.     

Frequency of reinforcement as a determinant of extinction-induced aggression during errorless discrimination learning.

Seven pigeons were trained to discriminate without errors between a green keylight and a dark key. The key-pecking response was reinforced in the presence of green, and extinction was in effect in the presence of the dark key. The opportunity to attack a restrained target pigeon was present only during extinction. Both variable-interval 30-sec and fixed-ratio 1 schedules of reinforcement during the positive stimulus induced a higher rate of attack during extinction than a variable-interval 5-min schedule. The highest rate of attack during extinction occurred during the first 20 sec after the positive stimulus terminated. Hence, the withdrawal of the positive condition, rather than the consequences of the pecking response during extinction, appears to be one of the primary factors responsible for attack between pigeons during extinction. Behavioral contrast, defined as a decrease in the rate of responding when the positive stimulus was presented alone, was obtained from the four birds that displayed the lowest overall rates of attack while the three birds with the highest attack rates did not display behavioral contrast. For the birds without contrast, components of the attack response during the positive stimulus presumably competed with and reduced the rate of pecking the key, thereby recluding behavioral contrast.     

Fixed-ratio escape and avoidance-escape from naloxone in morphine-dependent monkeys: effects of naloxone dose and morphine pretreatment.

Lever pressing by rhesus monkeys was maintained by morphine injections during four equally spaced sessions each day. During other periods, lever pressing was maintained by timeout from a continuous naloxone infusion (escape), or by timeout from a stimulus that preceded naloxone injections, or termination of the injections (avoidance-escape). As naloxone dose increased in the escape procedure, response rate increased to a maximum and then decreased. In the avoidance-escape procedure, response rate generally increased as naloxone dose increased, but the changes in rate were small compared to the excape procedure. Substitution of saline for naloxone in the escape procedure led to a very low response rates within three sessions. In the avoidance-escape procedure, rate decrements produced by saline substitution appeared to be related to the behavioral history of the monkey. Previous escape experience led to more rapid decreases in responding when saline was introduced, whereas responding was maintained for 15 sessions in a monkey without prior escape conditioning. Morphine pretreatment produced comparable, dose-dependent decreases in response rates in both procedures. The rate-decreasing effects of morphine were exacerbated when no naloxone was delivered in the escape procedure.     

Stimulus change as a factor in response maintenance with free food available.

Rats bar pressed for food on a reinforcement schedule in which every response was reinforced, even though a dish of pellets was present. Initially, auditory and visual stimuli accompanied response-produced food presentation. With stimulus feedback as an added consequence of bar pressing, responding was maintained in the presence of free food; without stimulus feedback, responding decreased to a low level. Auditory feedback maintained slightly more responding than did visual feedback, and both together maintained more responding than did either separately. Almost no responding occurred when the only consequence of bar pressing was stimulus feedback. The data indicated conditioned and sensory reinforcement effects of response-produced stimulus feedback.     

Transfer of hue matching in pigeons.

Pigeons were trained on a modified three-key matching-to-sample procedure, in which only one comparison key (rather than two) was lighted after an observing response to the center-key standard. Pecks on keys of matching comparison hues were reinforced. When non-matching hues appeared as the initially lighted comparisons, the nonmatching hue terminated and the matching hue appeared on the other side key only if the pigeon did not peck the nonmatching comparison for 4.8 sec. Pecks to the nonmatching hue reset the 4.8-sec delay interval. Three hues were used during acquisition. During transfer tests, two novel hues were substituted individually or together for one or two of the training hues. Latencies to the novel side-key hue were shortest when a novel matching hue appeared as the standard on the center key, and were essentially identical to baseline matching latencies. In contrast, when a novel hue appeared as either a standard or comparison in a nonmatching combination, latencies increased with increasing separation between the noevel hue and the nonmatching hue. These transfer data demonstrate the concept of hue matching.     

Some effects of response-independent reinforcement on auditory generalization gradients.

Two groups of six rats received discrimination training with two auditory stimuli differing in intensity. During one stimulus, the schedule was variable interval; during the other, it was either variable time or extinction. Both the variable time and extinction schedules resulted in differential rates of responding in the presence of the two stimuli. Extinction resulted in an earlier and more stable difference. Stimulus generalization gradients obtained along the noise-intensity dimension revealed peak shift with both procedures. In addition, a secondary peak to stimuli in between the two training stimuli occurred with the variable-time schedule.