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Results 501 - 550 of 1368
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Hermitte G - - 1992
A mild electrical shock delivered to the walking legs of the crab Chasmagnathus granulatus through a fine layer of sea water, induces a running response that declines after repeated stimulation. Herein, a first series of experiments was aimed at conditioning the response to a light or a dark pulse, but ...
Perone M - - 1992
Pigeons responded on fixed-ratio schedules ending in small or large reinforcers (grain presentations of different duration) interspersed within each session. In mixed-schedule conditions, the response key was lit with a single color throughout the session, and pausing was directly related to the past reinforcer (longer pauses after large reinforcers than ...
Alsop B - - 1992
Six pigeons were trained to discriminate between two intensities of white light in a symbolic matching-to-sample procedure. These stimuli were then used to signal which schedule was available on the main key in a switching-key concurrent schedule. The concurrent schedules led to a symbolic matching-to-sample phase in which the subject ...
Blough D S - - 1992
Pigeons pecked at one of two black forms, "+" or "O," either of which could appear alone on a white computer monitor screen. In baseline series of sessions, each form appeared equally often, and two pecks at it produced food reinforcement on 10% of trials. Test series varied the relative ...
Fetterman J G - - 1992
Pigeons' ability to discriminate stimulus duration, focusing on stimuli less than 1 s in duration, was evaluated in 4 experiments. In Experiment 1, the performances of pigeons and humans were compared with a staircase technique, and in Experiment 2, the method of constant stimuli was used. Both experiments produced similar ...
Freeman T J - - 1992
Pigeons were exposed to two different reinforcement schedules under different stimulus conditions in each of two daily sessions separated by 6 hr (Experiments 1 and 2) or in a single session (Experiment 3). Following this, either a fixed-interval (Experiment 1) or a variable-interval schedule (Experiments 2 and 3) was effected ...
Zygmont D M - - 1992
Two experiments demonstrated the efficacy of sample stimulus-control shaping programs for teaching arbitrary matching to 4 subjects who did not acquire the performances via standard methods (i.e., differential reinforcement and, in two cases, comparison intensity fading). All 4 had previously demonstrated identity matching with two-dimensional forms. Identity matching performances were ...
Allan R W - - 1991
Two experiments examined the effects of a negative (setback) response contingency on key pecking engendered by a changing light-intensity stimulus clock (ramp stimulus) signaling fixed-time 30-s food deliveries. The response contingency specified that responses would immediately decrease the light-intensity value, and, because food was delivered only after the highest intensity ...
Kohlenberg B S - - 1991
In Experiment 1, subjects acquired conditional equivalence classes controlled by three male and three female names as contextual stimuli. When equivalence relations were tested using new names not used in training (three male and three female), contextual control remained intact. Thus, generalized control of the composition of conditional equivalence classes ...
Smeets P M - - 1991
Previous research on humans suggests that simple discriminations may emerge if both stimuli, B1 and B2, are compounded with the stimuli of a previously trained discrimination, A1 (S+) and A2 (S-), and responding to the compounds, B1A1 and B2A2, is reinforced. Two questions were addressed. First, do simple discriminations also ...
McMillan D.E. - - 1991
An attempt was made to train pigeons to discriminate phencyclidine (PCP) from saline using a three-key color-tracking procedure under which birds were trained under a second order schedule [FR10 (FR5)] "without errors." Training without errors was done by not lighting the side key on which responses were not reinforced during ...
Remy M - - 1991
The eyes of the pigeon (Columba livia) are positioned laterally in the head. Thus, there is only a small area of binocular overlap, which constitutes the frontal visual field and a large area of monocular vision in the lateral visual fields. The conditions were examined under which intraocular transfer occurs ...
Fowler S C - - 1991
The behavioral effects of haloperidol (0.04 to 0.16 mg/kg) and nonparalytic doses of decamethonium (0.2 to 0.8 mg/kg) were studied with operant methods that permitted the measurement of response rate, peak force of response, duration of response, and duration of the rat's head entry into the reinforcement dipper well. Type ...
Kehoe E J - - 1991
Since Pavlov, theories of conditioning have assumed that CR evocation is governed by a series of internal stimuli generated by the CS. This hypothesis was tested in conditioning of the rabbit's nictitating membrane (NM) response by attempting to manipulate the internal sequence through truncating a delay CS and extending a ...
Preobrazhenskaya L A - - 1991
The dynamics of the changes in the number of instrumental motor reactions and in the frequency of cardiac contractions and of the theta rhythm of the hippocampus during the replacement of constant reinforcement by various schedules of probabilistic reinforcement of an alimentary conditional stimulus were investigated in three dogs. At ...
Alsop B - - 1991
The present study measured the effects of stimulus and reinforcer variations on pigeons' behavior in two different choice procedures. Two intensities of white light were presented as the stimuli on the main key in a switching-key concurrent schedule and as the sample stimuli in a signal-detection procedure. Under both procedures, ...
Brandon S E - - 1991
Three experiments showed the modulation of a rabbit eyeblink conditioned response (CR) to a Pavlovian conditioned stimulus (CS) by 30-s stimuli (A & B) that had been differentially paired with paraorbital shock. The CS (Y) was a 1,050-ms cue that had been paired with paraorbital shock outside A or B. ...
McLean A P - - 1991
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 ...
Kirkpatrick-Steger K - - 1991
In Experiment 1, classical conditioning of the rabbit's nictitating membrane response (NMR) was accomplished by pairing tone and light conditioned stimuli (CSs) with a shock unconditioned stimulus (UCS). MDA impaired the acquisition of conditioned responses (CR) to a tone-CS, while significantly enhancing CR acquisition to a light-CS. Experiment 2, employing ...
Nicol C J - - 1991
1. The aversiveness of motion and noise to broiler chickens was examined using a passive avoidance technique. Birds were initially trained to peck a key a fixed number of times to obtain food. After training, food could still be obtained by key pecking, but feeding was immediately followed by 1 ...
Lachnit H - - 1991
The experiment reviewed here merges Garner's (1974) distinction of separable and integral stimulus properties with the field of Pavlovian eyelid conditioning with human subjects. According to one rule, two sets of stimuli (separable vs integral) were constructed. A differential compound conditioning procedure was used with one group of subjects being ...
Neuenschwander-el Massioui N - - 1991
Multiunit activity (MUA) was chronically recorded in the hippocampal CA3 field of rats using a blocking paradigm with conditioned suppression of lever pressing for food as the measure of conditioning. In Experiment 1, a classical blocking paradigm demonstrated the good conditionability of 2 stimuli (a light and a tone) and ...
Stokes P D - - 1991
The effects of different shaping approximations on the topography of the rat's bar press were investigated in two experiments. Behavior was classified into discrete components, and changes in components and their sequential organization were analyzed. Experiment 1 examined response form early in training and found that specific components reinforced during ...
Preston R A - - 1991
The delay-reduction hypothesis of conditioned reinforcement states that the reinforcing value of a food-associated stimulus is determined by the delay to primary reinforcement signaled by the onset of the stimulus relative to the average delay to primary reinforcement in the conditioning situation. In contrast, most contemporary models of conditioned reinforcement ...
Edeline J M - - 1991
Highly specific subcortical receptive field (RF) plasticity was found in the dorsal division of the guinea pig medial geniculate body during cardiac conditioning to a tonal frequency. There was increased response to the conditioned-stimulus (CS) frequency, and there were decreased responses to adjacent frequencies, especially at the pretraining best frequency ...
Shah K - - 1991
Rats were trained under concurrent schedules consisting of two equal variable interval component schedules providing sucrose solutions of different concentrations (0.6 M, 0.2 M; 50 microliters in each case) as the reinforcers. The mean interreinforcement interval specified by the schedules was varied from 10 to 640 sec. Absolute response rate ...
Levey A B - - 1991
Recent reports of failure to obtain blocking in human galvanic skin response (GSR) conditioning, together with our own equivocal results with eyelid conditioning, have motivated us to re-examine the status of the conditioned stimulus (CS) in human conditioning studies. The issues raised by compound stimuli, by contextual cues and occasion ...
Reed P - - 1991
Four experiments examined the effects of increasing the number of food pellets given to hungry rats for a lever-press response. On a simple variable-interval 60-s schedule, increased number of pellets depressed response rates (Experiment 1). In Experiment 2, the decrease in response rate as a function of increased reinforcement magnitude ...
Durlach P J - - 1991
The stimuli that control responding in the peak procedure were investigated by training rats, in separate sessions, to make two different responses for food reinforcement. During one type of session, lever pressing was normally reinforced 32 s after the onset of a light. During the other type of session, chain ...
O'mara H - - 1991
The number of different ways of linking stimuli in the training phase of a conditional discrimination procedure designed to teach equivalence relations has hitherto been underestimated. An algorithm from graph theory that produces the correct number of such different ways is given. The establishment of equivalence relations requires transitive stimulus ...
Mace F C - - 1990
Adults with mental retardation in a group home received popcorn or coffee reinforcers for sorting plastic dinnerware. In Part 1 of the experiment, reinforcers were dispensed according to a variable-interval 60-s schedule for sorting dinnerware of one color and according to a variable-interval 240-s schedule for sorting dinnerware of a ...
Church R M - - 1990
Three facts of time perception are described based upon a temporal generalization task for rats (the peak procedure) in which food reinforcement is delivered on half the trials following the first lever-press response after some fixed interval after signal onset. (1) The mean response rate as a function of time ...
Wilson S R - - 1990
Following leads by Maslow (1964, 1968) and others who described peak experiences, this study was designed to learn more about the (1) subjective effects; (2) after-effects; and (3) interpretations of intense positive and negative experiences. Comparisons were made between respondents' "most positive" and "most negative" experiences and between these positive ...
Matzel L D - - 1990
In two experiments with the nudibranch mollusk Hermissenda, distinct characteristics of conditioned and unconditioned responses to high-speed orbital rotation were examined. In Experiment 1, two principle unconditioned responses to rotation were identified, namely, reduced rate of locomotion and contraction of the foot. The magnitude of the foot contraction increased throughout ...
McLaren I P - - 1990
In 1948 Konorski argued that conditioning reflects the strengthening of a connection between elements representing the signal and the reinforcer, as a result of the coincidence of activity in the signal element with a rise in activity in the reinforcer element. This Konorskian process represents one way of implementing an ...
Matzel L D - - 1990
Conditioned suppression of photokinesis by the marine mollusc Hermissenda was examined in 3 experiments. In each experiment, groups of animals received light (the conditioned stimulus, CS) that was paired with high-speed orbital rotation (the unconditioned stimulus, UCS), light and rotation explicitly unpaired, or no exposure to these stimuli. Twenty-four hours ...
White K G - - 1990
In a successive discrimination in which successively alternating red and green hues signaled component variable-interval schedules, sensitivity of the ratio of responses in the two components to variation in the component reinforcer ratio decreased systematically during the course of the component. This decrease in stimulus control or discrimination over the ...
Hall G A - - 1990
In two experiments, pigeons obtained food according to variable-interval schedules. In the first experiment, equivalent variable-interval schedules with average interreinforcer intervals ranging between 10 and 80 s in different conditions were studied in both open and closed economies. Response rates increased as reinforcement frequency decreased in the closed economy. By ...
Newland M C - - 1990
The behavioral effects of amphetamine and pentobarbital depend upon the conditions maintaining behavior. For example, amphetamine usually decreases the rate of operant behavior maintained by fixed ratio schedules while pentobarbital either increases it or leaves it unaffected. However, when considerable exertion is required, as in situations that require endurance, amphetamine ...
Nevin J A - - 1990
Two multiple-schedule experiments with pigeons examined the effect of adding food reinforcement from an alternative source on the resistance of the reinforced response (target response) to the decremental effects of satiation and extinction. In Experiment 1, key pecks were reinforced by food in two components according to variable-interval schedules and, ...
Honey R C - - 1990
Three experiments used rats as subjects to investigate the generalization of conditioned responding between stimuli as a function of the subjects' exposure to these cues prior to conditioning. Experiment 1 used a between-subjects design, food as the reinforcer, and measured the tendency of subjects to approach the site of food ...
Minor T R - - 1990
Six experiments examined the effects of signaling the termination of inescapable shock (cessation conditioning) or shock-free periods (backward conditioning) on later escape deficits in the learned helplessness paradigm, using rats (Sprague-Dawley and Bantin-Kingman). A cessation signal prevented later performance deficits when highly variable inescapable shock durations were used during pretreatment. ...
Lederhendler I I - - 1990
Classical conditioning of the marine snail Hermissenda can be produced in a single session of 50 pairings of light and rotation stimuli. Voltage clamp measurements of two outward K+ currents, IA and ICa2(+)-K+ were obtained from medial Type B photoreceptors that were isolated from the nervous system 1 day after ...
Dunn R - - 1990
Pigeons responded on concurrent chains with equal initial- and terminal-link durations. In all conditions, the terminal links of one chain ended reliably in reinforcement; the terminal links on the alternative chain ended in either food or blackout. In Experiment 1, the terminal-link stimuli were correlated with (signaled) the outcome, and ...
Weisz D J - - 1990
The presentation of a neutral or conditioned stimulus (CS) at an appropriate interval prior to the presentation of a corneal airpuff, or a paraorbital shock (unconditioned stimulus, US) can facilitate the amplitude of the unconditioned nictitating membrane (NM) response in rabbit. In two experiments, it was demonstrated that an associative ...
Palya W L - - 1990
Six experiments were used to examine the effects of explicit response, stimulus, and temporal dependencies on responding in an interfood interval. The first two experiments demonstrated that 10-segment 60-s interfood clocks controlled similar distributions of key pecking in pigeons regardless of whether response-reinforcement contiguity was required, allowed, or precluded. The ...
Dunn R - - 1990
Response-contingent timeouts of equal duration and frequency were added to both alternatives of unequal concurrent schedules of reinforcement. For each of 4 pigeons in Experiment 1, relative response rates generally became less extreme as the frequency of timeout increased. In Experiment 2, relative response rates consistently approached indifference as the ...
Mazur J E - - 1990
This experiment measured pigeons' choices between delayed reinforcers and fixed-ratio schedules in which a force of approximately 0.48 N was needed to operate the response key. In ratio-delay conditions, subjects chose between a fixed-ratio schedule and an adjusting delay. The delay was increased or decreased several times a session in ...
Murua V S - - 1990
Rats exposed to one, three, or seven conditioning sessions defined by an olfactory conditioned stimulus and stress or antidepressant administration as unconditioned stimulus were later tested for their preference for the conditioned olfactory stimulus. A significant reduction of the time spent in the conditioned stimulus was observed in animals exposed ...
King G R - - 1990
Two experiments examined human subjects' sensitivity to variation in reinforcer amount under different methods of reinforcer delivery. Subjects chose between schedules varying in terms of amount and/or delay of reinforcement, the reinforcer being points exchangeable for money. In Experiment 1, reinforcer amount was manipulated by varying the monetary value of ...
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