飞行场景中表征动量的地标吸引效应和排斥效应

设置了安全和危险两种地标, 采用诱导运动范式考察了飞行场景中运动目标和关联地标的相对关系、目标运动方向及关联地标的意义特征和呈现时间对运动目标位置判断的影响。结果显示: (1)飞行场景中飞机的表征动量较强; (2) 趋近安全地标的表征动量大于远离安全地标的表征动量, 趋近危险地标的表征动量小于远离危险地标的表征动量, 安全地标呈现出地标吸引效应, 而危险地标呈现出地标排斥效应; (3) 高关联的安全和危险地标使飞机的表征动量不受运动方向影响; (4) 保持间隔期间呈现的安全和危险地标使飞机的表征动量增加。结论 :表征动量的地标效应受制于地标意义特征, 表征动量受到目标和地标之间的因果关系和情景意义的影响。     

Employing multiple theories and evoking new ideas: the use of clinical material

In this paper, I wish to illustrate how working with a patient who had a certain kind of narcissistic difficulty led me to develop particular clinical strategies to facilitate the development of a sturdier sense of self, greater affect tolerance and modulation, the diminution of harshness of her superego, and the ownership of projected parts of herself, and to decrease paranoid ideation. I call upon concepts from various theoretical schools of psychoanalysis to make sense of the dynamic intricacies of the patient's psychological organization as they revealed themselves in the analytic process. These conceptualizations of the patient's difficulties and of clinical interventions to address them result in a hybrid theory of both theory and technique. What transpired in the clinical work also led me to propose an additional way to understand this kind of patient's difficulties with accepting interpretations or any view that differed from the patient's subjectivity. I am proposing that 'otherness' itself, rather than only specific conflictual aspects of the self, is disowned. It is the analyst's empathic stance toward all that is repudiated--the specific disowned aspects of the self and 'otherness' itself--along with empathy for the patient's conscious state that will enable reinternalization and ultimately healing.     

Relative reinforcer rates and magnitudes do not control concurrent choice independently

One assumption of the matching approach to choice is that different independent variables control choice independently of each other. We tested this assumption for reinforcer rate and magnitude in an extensive parametric experiment. Five pigeons responded for food reinforcement on switching-key concurrent variable-interval variable-interval schedules. Across conditions, the ratios of reinforcer rates and of reinforcer magnitudes on the two alternatives were both manipulated. Control by each independent variable, as measured by generalized-matching sensitivity, changed significantly with the ratio of the other independent variable. Analyses taking the model-comparison approach, which weighs improvement in goodness-of-fit against increasing number of free parameters, were inconclusive. These analyses compared a model assuming constant sensitivity to magnitude across all reinforcer-rate ratios with two alternative models. One of those alternatives allowed sensitivity to magnitude to vary freely across reinforcer-rate ratios, and was less efficient than the common-sensitivity model for all pigeons, according to the Schwarz-Bayes information criterion. The second alternative model constrained sensitivity to magnitude to be equal for pairs of reinforcer-rate ratios that deviated from unity by proportionately equal amounts but in opposite directions. This model was more efficient than the common-magnitude-sensitivity model for 2 of the pigeons, but not for the other 3. An analysis of variance, carried out independently of the generalized-matching analysis, also showed a significant interaction between the effects of reinforcer rate and reinforcer magnitude on choice. On balance, these results suggest that the assumption of independence inherent in the matching approach cannot be maintained. Relative reinforcer rates and magnitudes do not control choice independently.     

SENSITIVITY OF CONDITIONAL-DISCRIMINATION PERFORMANCE TO WITHIN-SESSION VARIATION OF REINFORCER FREQUENCY

The present experiment developed a methodology for assessing sensitivity of conditional-discrimination performance to within-session variation of reinforcer frequency. Four pigeons responded under a multiple schedule of matching-to-sample components in which the ratio of reinforcers for correct S₁ and S₂ responses was varied across components within session. Initially, five components, each arranging a different reinforcer-frequency ratio (from 19 to 91), were presented randomly within a session. Under this condition, sensitivity to reinforcer frequency was low. Sensitivity failed to improve after extended exposure to this condition, and under a condition in which only three reinforcer-frequency ratios were varied within session. In a later condition, three reinforcer-frequency ratios were varied within session, but the reinforcer-frequency ratio in effect was differentially signaled within each component. Under this condition, values of sensitivity were similar to those traditionally obtained when reinforcer-frequency ratios for correct responses are varied across conditions. The effects of signaled vs. unsignaled reinforcer-frequency ratios were replicated in two subsequent conditions. The present procedure could provide a practical alternative to parametric variation of reinforcer frequency across conditions and may be useful in characterizing the effects of a variety of manipulations on steady-state sensitivity to reinforcer frequency.     

EVALUATION OF THE MULTIPLE-STIMULUS WITHOUT REPLACEMENT PREFERENCE ASSESSMENT METHOD USING ACTIVITIES AS STIMULI

The current study examined the accuracy of the multiple-stimulus without replacement (MSWO) preference assessment for identifying preferred common classroom activities as reinforcers with children with behavioral disorders. The accuracy of predictions from the MSWO regarding high, medium, and low stimulus preference was tested by providing contingent access to activities for completing math problems within an independent seatwork format. Overall, there was an interaction effect between preference ranking (high, medium, or low) and number of problems completed. The results confirm and extend previous findings regarding the accuracy of predictions with the MSWO. The findings also reveal, however, some individual differences that may account for instances in which student behavior did not conform to predictions of stimulus preference assessments.     

THE EFFECTS OF VARIED VERSUS CONSTANT HIGH‐, MEDIUM‐, AND LOW‐PREFERENCE STIMULI ON PERFORMANCE

The purpose of the current study was to compare the delivery of varied versus constant high‐, medium‐, and low‐preference stimuli on performance of 2 adults on a computer‐based task in an analogue employment setting. For both participants, constant delivery of the high‐preference stimulus produced the greatest increases in performance over baseline; the varied presentation produced performance comparable to constant delivery of medium‐preference stimuli. Results are discussed in terms of their implications for the selection and delivery of stimuli as part of employee performance‐improvement programs in the field of organizational behavior management.     

ISOLATING BEHAVIORAL MECHANISMS OF INTERTEMPORAL CHOICE: NICOTINE EFFECT ON DELAY DISCOUNTING AND AMOUNT SENSITIVITY

Many drugs of abuse produce changes in impulsive choice, that is, choice for a smaller—sooner reinforcer over a larger—later reinforcer. Because the alternatives differ in both delay and amount, it is not clear whether these drug effects are due to the differences in reinforcer delay or amount. To isolate the effects of delay, we used a titrating delay procedure. In phase 1, 9 rats made discrete choices between variable delays (1 or 19 s, equal probability of each) and a delay to a single food pellet. The computer titrated the delay to a single food pellet until the rats were indifferent between the two options. This indifference delay was used as the starting value for the titrating delay for all future sessions. We next evaluated the acute effects of nicotine (subcutaneous 1.0, 0.3, 0.1, and 0.03 mg/kg) on choice. If nicotine increases delay discounting, it should have increased preference for the variable delay. Instead, nicotine had very little effect on choice. In a second phase, the titrated delay alternative produced three food pellets instead of one, which was again produced by the variable delay (1 s or 19 s) alternative. Under this procedure, nicotine increased preference for the one pellet alternative. Nicotine‐induced changes in impulsive choice are therefore likely due to differences in reinforcer amount rather than differences in reinforcer delay. In addition, it may be necessary to include an amount sensitivity parameter in any mathematical model of choice when the alternatives differ in reinforcer amount.     

Within-session changes in responding during several simple schedules

Pigeons' key pecking was reinforced by food delivered by several fixed-interval, variable-ratio, and differential-reinforcement-of-low-rate schedules. Rate of responding, number of responses per reinforcer, length of postreinforcement pause, running response rate, and the time required to collect an available reinforcer changed systematically within sessions when the schedules provided high rates of reinforcement, but usually not when they provided low rates. These results suggest that the factors that produce within-session changes in responding are generally similar for different schedules of reinforcement. However, a separate factor may also contribute during variable-ratio schedules. The results question explanations for within-session changes that are related solely to the passage of time, to responding, and to one interpretation of attention. They support the idea that one or more factors related to reinforcement play a role.     

Reinforcer magnitude (sucrose concentration) and the matching law theory of response strength

This experiment investigated the relationship between reinforcer magnitude (sucrose concentration) and response rate. The purpose was to evaluate the behavior of two parameters of an equation that predicts absolute response rate as a function of reinforcement rate and two free parameters. According to Herrnstein's (1970) theory of reinforced behavior, one parameter of this "response-strength equation" measures the efficacy of the reinforcer maintaining responding and the other parameter measures motoric components of response rate, such as response duration. Seven rats served as subjects. Experimental sessions consisted of a series of five different variable-interval schedules of reinforcement, each in effect for 5 minutes. Within each session, obtained reinforcement rates varied over more than a 30-fold range, from about 20 per hour to 700 per hour. The reinforcer was sucrose solution, and, between sessions, its concentration was varied from 0.0 to 0.64 molar (0 to 21.9%). For sucrose concentrations of 0.16 to 0.64 m, response rate was a negatively accelerated function of reinforcement rate. Increases in sucrose concentration increased response rates maintained by low but not high reinforcement rates. This pattern of changes corresponds to a change in the reinforcement-efficacy parameter of the response-strength equation. In contrast, the motor-performance parameter did not change as a function of sucrose concentration. These findings are inconsistent with the results of a similar study (Bradshaw, Szabadi, & Bevan, 1978) but support Herrnstein's theory of reinforced behavior.     

The control of choice by its consequences

Five pigeons were trained on concurrent variable-interval schedules in which equal rates of reinforcement were always arranged for left- and right-key responses, but different overall rates were signaled by key colors. Sessions began with both keys lit yellow for the instrumental phase. If, after 20 s of this phase, the relative number of responses that had been made to the left key equaled or exceeded .75, both keys changed red for the contingent phase. The contingent phase arranged another concurrent variable-interval schedule for a further 20 s before the instrumental phase was reinstated. However, if preference in the instrumental phase did not exceed .75, the instrumental phase continued for a further 20 s before preference was again compared with the criterion. In Part 1, the reinforcer rate arranged in the instrumental phase was held constant at 4.8 reinforcers per minute, while the reinforcer rate arranged in the contingent phase was varied across conditions from 0 to 19.2 over five steps. In Part 2, reinforcer rates in the contingent phase were kept constant at 36 per minute, while reinforcer rates in the instrumental phase were varied from 0 to 36 over seven steps. Part 3 replicated Part 2 but used reinforcer rates in both phases that were one third of those arranged in Part 2. Measures of choice obtained by summing responses across presentations of the instrumental phase became more extreme toward the left key as the reinforcer rate obtained in the contingent phase was increased (Part 1) and as the reinforcer rate obtained in the instrumental phase was decreased (Parts 2 and 3). Changes in these measures of choice were accompanied by systematic changes in the relative frequency with which the criterion was exceeded. Changes in both these measures were correlated with changes in the relative frequency with which subjects responded exclusively to the left key. These results are discussed with respect to the two choices that were concurrently available in this procedure and the response alternatives that might constitute the concurrent operants in each choice.