Stimuli, reinforcers, and behavior: an integration

We propose that a fundamental unit of behavior is the concurrent discriminated operant, and we discuss in detail a quantitative model of the concurrent three-term contingency that is based on the notion that an animal's behavior is controlled to differing extents by both stimulus—behavior and behavior—reinforcer relations. We show how this model can describe performance in a variety of experimental procedures: conditional discrimination and matching to sample, both with and without reinforcement for responses that are traditionally identified as errors; conditional discrimination with more than two stimuli and choice alternatives; delayed matching to sample and delayed reinforcement in matching to sample; second-order and complex conditional discrimination; and multiple and concurrent schedules. Although the model is incomplete in its coverage, and may be incorrect, we believe that this conceptual approach will bear fruit in the development of behavior theory.     

Falsification of matching theory: changes in the asymptote of Herrnstein''s hyperbola as a function of water deprivation.

Five rats pressed levers on variable-interval schedules of water reinforcement at various levels of water deprivation. In one phase of the experiment, three deprivation conditions that replicated conditions in Heyman and Monaghan (1987) were arranged, along with three less extreme deprivation conditions. In a second phase, water deprivation was arranged so that subjects were exposed to a greater range of access to water per day. Herrnstein's hyperbola described the rats' response-rate data well. The y asymptote, k, of the hyperbola appeared roughly constant over the conditions that replicated those of Heyman and Monaghan, but decreased markedly when less extreme deprivation conditions were included. In addition, k varied systematically when the second method of arranging deprivation was used. These results falsify a strong form of matching theory and confirm predictions made by linear system theory.     

Interresponse-time sensitivity during discrete-trial and free-operant concurrent variable-interval schedules

Two experiments investigated the sensitivity of pigeons' choice to elapsed time since the last response (i.e., to inter-response time [IRT]) during concurrent variable-interval variable-interval schedules. Experiment 1 used a two-key discrete-trial procedure with variable intertrial intervals. Experiment 2 employed a three-key free-operant procedure. In both experiments choice was found to be a function of the active-schedule IRT, defined as the time since the most recent response. Monte Carlo simulations show how this finding permits the joining of several seemingly incompatible data sets held to both support and contradict a kind of choice strategy, termed momentary maximizing, which attempts to maximize momentary reinforcement probabilities. The studies suggest that only two variables are needed to describe the static molecular structure of concurrent variable-interval choice: active-schedule IRTs and "response states" consisting of the last one or two schedule choices.     

山东沿海地区大学生日常时间用语词义赋值的研究

本研究运用模糊统计试验的方法对五组日常时间用语词进行了经验赋值 ,被试是 3 1 2名大学生。结果表明 :(1 )被试对日常时间用语词词义的理解是模糊的 ,其赋值指向较大的区间 ;(2 )被试对日常时间用语词的赋值受词自身具有的数值的影响 ,受词的下属时间单位数量的影响 ;(3 )词义相近的词赋值亦接近 ;(4)对表示人的年龄的词的赋值因对象的性别、词的熟悉性和赋值区间的封闭性的不同而不同 ;(5 )“几”在表示时间的数量时对应的赋值区间是3～ 5     

时距知觉的心理学研究

本文回顾了近五十年来时距知觉的实验研究,对不同的理论模型、实验范式、实验方法以及主要时距判断规律作了较全面的评述,并进一步探讨了时距知觉研究未来的发展。     

Reduction of stimulus overselectivity with nonverbal differential observing responses

Three individuals with mental retardation exhibited stimulus overselectivity in a delayed matching-to-sample task in which two sample stimuli were displayed on each trial. Intermediate accuracy scores indicated that participants could match one of the samples but not both of them. Accuracy in a baseline condition was compared to accuracy with a differential observing response procedure. This procedure prompted participants to make simultaneous identity-matching responses that required observation and discrimination of both sample stimuli. These observing responses were never followed by differential consequences. When observing responses were prompted, participants' accuracy scores improved. In a return to the baseline condition, when differential observing responses were no longer prompted, accuracy returned to intermediate levels. The results show that stimulus overselectivity can be greatly reduced by a behavioral intervention that controls observing behavior and verifies discrimination, but that exposure to such procedures alone may be insufficient for lasting benefits.     

CONSTRUCTED-RESPONSE MATCHING TO SAMPLE AND SPELLING INSTRUCTION

The development of interactive programmed instruction using a microcomputer as a teaching machine is described. The program applied a constructed-response matching-to-sample procedure to computer-assisted spelling instruction and review. On each trial, subjects were presented with a sample stimulus and a choice pool consisting of 10 individual letters. In initial training, sample stimuli were arrays of letters, and subjects were taught to construct identical arrays by touching the matching letters in the choice pool. After generalized constructed-response identity matching was established, pictures (line drawings) of common objects were presented as samples. At first, correct spelling was prompted by also presenting the printed name to be “copied” via identity matching; then the prompts were faded out. The program was implemented with 2 mentally retarded individuals. Assessment trials determined appropriate words for training. Correct spelling was established via the prompt-fading procedure; training trials were interspersed among baseline trials that reviewed and maintained spelling of previously learned words. As new words were learned, they were added to a cumulative baseline to generate an individualized review and practice battery for each subject.     

Discrimination training facilitates pigeons' performance on one-trial-per-day delayed matching of key location

Six pigeons were tested on a one-trial-per-day variant of delayed matching of key location. In one condition, a trial began with the illumination of a pair of quasi-randomly selected pecking keys in a large 10-key test box. Pigeons' pecks to one key (the sample) were reinforced with 8-second access to grain on a variable-interval 30-second schedule, whereas pecks to the other key (the distractor) had no scheduled consequences. In the second condition, the nonreinforced distractor was not presented. In both conditions, subjects were removed from the apparatus after 15 minutes and placed in a holding cage. Subjects were subsequently replaced in the box after a delay (retention interval) of 30 seconds and were reexposed to the illuminated sample and distractor keys for 1 minute. If a pigeon made more pecks to the sample during this interval, the distractor was extinguished and subsequent pecks to the sample were reinforced on the previous schedule for an additional 15 minutes. If, however, a pigeon made more pecks to the distractor, both keys were extinguished and the subject was returned to its home cage. For all subjects, matching-to-sample accuracy was higher in the first condition. In a second experiment, the retention interval was increased to 5, 15, and 30 minutes, and then to 1, 2, 4, 8, 12, and 24 hours. Most subjects remembered the correct key location for up to 4 hours, and in one case, up to 24 hours, demonstrating a spatial-memory proficiency far better than previously reported in this species on delayed matching tasks. The results are discussed in terms of the commonly held distinction between working and reference memory.     

Local contrast in behavior allocation during multiple-schedule components

Allocation of responses between two keys was studied during two alternating multiple-schedule components. Responses were recorded in successive quarters of each component. Variable-interval reinforcer schedules on the two keys were constant throughout the experiment for one (constant) component and were varied over conditions on one key for the other, producing changes in reinforcer ratios for the varied component. Behavior allocation for the first quarter of the constant component was inversely related to varied-component reinforcer ratios, a form of local contrast, but this relationship was not observed later in the component. During the first quarter of the varied component, slopes of matching lines were high and decreased later in the component. It is argued that this form of local contrast cannot be explained in terms of reallocation of extraneous reinforcers between components, and that the matching law for concurrent operants does not capture some sources of control over behavior allocation. A simple extension of the matching law is offered that adequately describes behavior changes during both components. A version of this formulation can predict contrast effects in absolute response rates.     

Protocol analysis of the correspondence of verbal behavior and equivalence class formation.

In two equivalence experiments, a "think aloud" procedure modeled after Ericsson and Simon's (1980) protocol analysis was implemented to examine subjects' covert verbal responses during matching to sample. The purpose was to identify variables that might explain individual differences in equivalence class formation. The results from Experiment 1 suggested that subjects who formed equivalence classes described the relations among stimuli, whereas those not showing equivalence described sample and comparison stimuli as unitary compounds. Because Experiment 1 only demonstrated a correlation between describing stimulus compounds and the absence of equivalence classes, a second study was conducted. In Experiment 2, equivalence class formation was brought under experimental control through pretraining manipulations that facilitated responding either to stimulus compounds or to relations among stimuli. The results demonstrated that a history of describing stimulus compounds, when compared with describing the relations among the stimuli, interfered with the emergence of stimulus equivalence. These findings clarify individual differences in stimulus equivalence. They also demonstrate the utility of analyzing verbal reports to identify possible variables that can be manipulated experimentally.