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1.
[Correction Notice: An erratum for this article was reported in Vol 25(3) of Canadian Journal of Psychology Revue Canadienne de Psychologie (see record 2007-04520-001). In diagram appearing in this erratum should be substituted for the diagram appearing as Figure 2 on p. 423 of the article.] Measured the GSR and digital volume-pulse change in 4 groups of 80 Ss each with light and tone as CS and shock as UCS. For Groups I and II, the CS-UCS interval was .75 and 7.5 sec., respectively; for Groups III and IV, the UCS-CS interval was .75 and 7.5 sec., respectively. Group III showed "backward" differential conditioning in the GSR; Group II yielded reliable conditioning of "multiple responses" occurring before UCS onset; the magnitude and extent of conditioning was greater in Group I than in Groups II and III, which did not differ; some evidence for "reverse" conditioning was suggested in Group IV, with slightly greater responding to the CS not paired with the UCS; instructions which distracted 1/2 the Ss from the CS did not affect responding to those stimuli. (French summary) (16 ref.) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

2.
Three experiments demonstrated that human newborn heart rate level can be reliably modified through classical conditioning procedures. The theory of sensitization served as a frame of reference for Exps I and II, and drive reduction served for Exp III. In Exp I the delay, delay-trace, and control groups, with 10 2-day-old newborns in each, received 5 preconditioning trials of the CS alone, 16 conditioning trials with CS–UCS pairings differing for each group, and 5 extinction trials. Exp II was a replication of the 1st study and involved only the delay and delay-trace groups with 10 infants each. In both studies the delay group curves showed significant monophasic acceleratory responses during extinction. Results support the sensitization hypothesis (i.e., the CR occurring in the interstimulus interval was fashioned out of the response to the CS). In Exp III, the measure of conditioning was the response to the probe technique. 10 experimental Ss received preconditioning trials of nitrogen puff (UCS?) administered to the abdomen, followed by 10 CS–UCS? (500-Hz tone acetic acid) pairings with an interstimulus interval of 3 sec. 10 controls received the same design with a CS–UCS? interval of 40 sec. Analyses of the probe stimulus trials showed significant changes for the control group and none for the experimental group. The CS–UCS? pairings in the experimental group are interpreted as producing increased drive and adaptive damping of the heart rate response. Findings show that early learning may occur under a variety of conditions and that the results can be incorporated by different theories. (79 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

3.
Examined acquisition of the rabbit's nictitating membrane response to a light?+?tone simultaneous compound stimulus and its components as a function of the intensity of the tone. In Exp I, the tone intensity was varied across the values of 85, 89, and 93 db, and the CS–UCS interval was 400 msec. In Exp II, the tone intensities were 73, 85, and 93 db, and the CS–UCS interval was 800 msec. Exps III and IV further examined the effects of the 73-db CS–UCS tone at CS–UCS intervals of 400 and 800 msec. All experiments included control groups, which were trained with either a light or a tone CS. Overall results show repeated instances of overshadowing: the impairment of CR acquisition to one or both of the components of a compound. Two types of summation were obtained: within-Ss summation, in which Ss trained with a compound showed a higher level of responding to the compound than to either of its component CSs; and between-groups summation, in which a group trained with a compound showed faster CR acquisition than either of its corresponding control groups trained with a single CS. Results are discussed in terms of perceptual and distributive processing models of compound stimulus conditioning. (37 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

4.
22 normals and 22 schizophrenics underwent differential conditioning of the GSR, using 8-sec tones of differing frequencies as the CSs, an 8-sec CS-UCS interval, and a UCS comprised of an RT task signaled by a low-intensity light. Both intertrial reports and postconditioning interviews were obtained. 12 Ss in the normal group verbalized the CS relations accurately, compared to 3 Ss in the schizophrenic group. The normal group showed significant GSR differentiation, though conditioning was limited to the group of accurately verbalizing Ss. No evidence for conditioning was obtained in the schizophrenic group. Normal Ss had faster RTs than schizophrenic Ss. The RT of accurately verbalizing normals was shorter than that of inaccurately verbalizing normals, and the degree of GSR differentiation was significantly correlated with RT. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

5.
The interval between exposure to a CS to male quail and access to a female (the unconditioned stimulus [UCS]) was varied from 0.5 to 20 min using a Pavlovian delayed conditioning procedure. Increasing the CS–UCS interval altered the spatial distribution of sexual conditioned behavior. With a short CS–UCS interval (1 min), conditioning resulted in the Ss remaining close to the CS and increasing their locomotor behavior near the CS. With a long CS–UCS interval (20 min), the Ss approached the CS to some degree, but their locomotor behavior was increased in areas farther removed from the CS. Results are interpreted within the context of a behavior systems approach to the study of learning and indicate that the typical finding of an inverse relation between conditioned responding and the CS–UCS interval may be an artifact of the use of a limited range or behavioral measures. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

6.
In 2 experiments, 36 New Zealand albino rabbits received classical conditioning of the nictitating membrane response in a trace conditioning paradigm. In this paradigm, a 250-msec tone conditioned stimulus (CS) occurred, after which there was a 500-msec period of time in which no stimuli occurred (the trace interval), followed by a 100-msec air-puff unconditioned stimulus (UCS). In Exp I, lesions of the hippocampus or cingulate/retrosplenial cortex (CRC) disrupted acquisition of the long-latency or adaptive conditioned response (CR) relative to unoperated controls and Ss that received neocortical lesions that spared the CRC. When Ss with hippocampal or CRC lesions were switched to a standard delay paradigm in which the CS and UCS were contiguous in time, they acquired in about the same number of trials as naive Ss. In Exp II, multiple-unit activity in area CA1 of the hippocampus was examined during acquisition of the trace CR. Ss had a 500-msec trace interval (Group T-500), received explicitly unpaired presentations of the CS and UCS, or underwent conditioning with a 2-sec trace interval. Group T-500 acquired the CR in about 500 trials. Early in training, there was a substantial increase in neuronal activity in the hippocampus that began during the CS and persisted through the trace interval. Later in conditioning as CRs emerged, the activity shifted to later in the trace interval and formed a model of the amplitude–time course of the behavioral CR. (65 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

7.
Studied the role of the relative durations of CS–UCS gap and intertrial interval (ITI) in 2 autotracing experiments. In Exp I, CS–UCS gap duration was held constant at 12 sec, and the ITI was systematically varied between 15 and 240 sec across 5 groups of 6 female White Carneaux pigeons. Conditioned excitation (CS-approach) emerged at ITIs of greater than 60 sec, and conditioned inhibition (CS-withdrawal) emerged at ITIs of less than 60 sec. In Exp II, with 50 Ss, the time between successive UCSs averaged 87 sec, and the duration of the CS–UCS gap varied from 6 to 72 sec. CS-approach was observed only in the 6-sec gap condition, and CS-withdrawal developed with gaps of 24 sec or more. Findings indicate that the relative durations of CS–UCS gap and the ITI are more important than is the absolute degree of CS–UCS contiguity in determining whether and what type of conditioning occurs on trace arrangements. (35 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

8.
Context–UCS associations have been suggested as the mediator of the response decrement that occurs when extra UCSs are added to the intertrial intervals (ITIs) of a standard Pavlovian conditioning situation. The present autoshaping experiments were concerned with the effect of signaling those extra UCSs, since such signaling might be expected to lessen their ability to condition the context. In Exp I, 16 female Carneaux pigeons were trained in Skinner boxes before receiving pretraining with the CS to be used as the signal of the ITI UCSs. During the main training, Ss were given autoshaping with a keylight CS. Exp II used a tone CS with 31 Ss. Results show that signaling the ITI UCSs did reduce their detrimental effects in responding to the CS. To determine whether that reduction was due to an impact of signaling on the target-CS/UCS association or on performance to the target-CS, Exp III examined responding to differentially trained CSs in a common context, as well as responding to identically trained CSs in differentially trained contexts with 32 Ss. More responding occurred to the CS trained with signaled, as compared with unsignaled, ITI UCSs; further, there was more responding to that CS in the more highly valued context. Results suggest that contextual value does interact with CS–UCS learning and may also affect performance to the CS. (42 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

9.
Three experiments, with 118 Sprague-Dawley rats, assessed conditioned analgesia in a Pavlovian 2nd-order conditioning procedure by using inhibition of responding to thermal stimulation as an index of pain sensitivity. In Exp I, Ss receiving 2nd-order conditioning showed longer response latencies during a test of pain sensitivity in the presence of the 2nd-order conditioned stimulus (CS) than Ss receiving appropriate control procedures. Exp II found that extinction of the 1st-order CS had no effect on established 2nd-order conditioned analgesia. Exp III evaluated the effects of post 2nd-order conditioning pairings of subcutaneous morphine sulfate (10–20 mg/kg) and the shock unconditioned stimulus/stimuli (UCS). Ss receiving paired morphine–shock presentations showed significantly shorter response latencies during a hot-plate test of pain sensitivity in the presence of the 2nd-order CS than did Ss receiving various control procedures; 2nd-order analgesia was attenuated. Data extend the associative account of conditioned analgesia to 2nd-order conditioning situations and are discussed in terms of the mediation of both 1st- and 2nd-order analgesia by an association between the CS and a representation or expectancy of the UCS, which may directly activate endogenous pain inhibition systems. (52 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

10.
Preconditioning experience with the UCS retards subsequent excitatory conditioning. Three experiments demonstrated that the UCS retardation effect is attenuated by associative manipulations of contextual stimuli of the UCS preexposure environment. The UCS retardation effect was reduced by (a) altering contextual stimuli between preexposure and conditioning (Exp I, 49 New Zealand male rabbits; Exp II, 28 Ss); and (b) latently inhibiting contextual stimuli subsequent to UCS (Exp III, 36 Ss). Although UCS preexposure retarded excitatory conditioning, results of Exp IV (48 Ss) demonstrated that UCS preexposure facilitated inhibitory conditioning. Overall findings indicate that an association between contextual stimuli and preexposed UCS contributes to the effects of preconditioning UCS experience on subsequent learning. (48 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

11.
Two experiments, with 88 female albino rabbits, investigated conditioning of the nictitating membrane response to a reinforced serial compound stimulus. The serial compound was composed of a 400-msec CS (CSA), a trace interval of at least 2 sec, and a brief 2nd CS (CSB) prior to the UCS. The CSB duration was either 150, 250, or 400 msec in Exp I, and the CSB duration in Exp II was 400 msec. Exp I compared serial compound training to an "uncoupled" condition, which contained intermixed CSA–UCS trials and CSB–UCS trials. Exp II compared serial compound training with uncoupled training, 2nd-order conditioning (CSA–CSB/CSB–UCS), trace conditioning (CSA–UCS), and generalization testing that entailed CSB–UCS training and unreinforced tests with CSA. The serial compound, uncoupled, and 2nd-order conditioning procedures all produced high levels of responding during CSA, but only the reinforced serial compound procedure yielded an appreciable likelihood of CR initiation during the trace interval between CSA and CSB. The CRs during the trace interval were temporally distinct from the CRs during CSA and did not appear to be belated CRs to CSA itself. Results are discussed in connection with stimulus selection phenomena, for example, overshadowing and potentiation of toxicosis conditioning. (46 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

12.
Using conditioned suppression of barpressing to investigate the stability of a conditioned stimulus–unconditioned stimulus (CS–UCS) association, the present authors gave 151 water-deprived rats either a few pairings of the CS with a strong footshock UCS or many pairings with a weak footshock UCS so that barpress suppression in response to CS was equated. Exp I established training parameters that yielded this equivalence. Specifically, rapid acquisition to a preasymptotic level of responding with strong shock produced suppression comparable to the asymptotic level reached more slowly with weak shock. Exp II showed that although equivalent performance was obtained from extensive conditioning with a weak shock or limited conditioning with a strong shock, only extensive conditioning with weak shock resulted in retarded acquisition of an association between that same CS and a footshock level perceived as midway between the 2 initial training shock intensities as implied by asymptotic performance in Exp I. Exp III demonstrated that the observed retardation in Ss given many conditioning trials with weak shock was CS-specific. It is concluded that the malleability of learned behavior is not simply a function of initial associative strength but is dependent on the path during initial acquisition. (18 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

13.
Three experiments used an autoshaping procedure in 64 female White Carneaux pigeons to investigate the conditioning of the context and of a discrete CS with a food UCS. CS–UCS associations were measured by directed pecking at the key light CS; context–UCS associations were assessed by general activity in the context. Exp I investigated the influence of context–UCS associations on performance to a previously trained CS. The same CS produced greater keypecking in a context of higher associative strength. Exp II examined the influence of context–UCS associations on learning of CS–UCS associations. When tested in a context of fixed associative strength, a CS that had been trained in a context of high associative strength elicited less responding than one trained in a context of low associative strength. Exp III found that signaling a UCS by a discrete CS interfered with the formation of context–UCS associations, as measured both in terms of general activity and ability to promote responding to another CS. Results suggest that the context and the CS compete for association with the UCS. They also suggest that context–UCS associations facilitate the exhibition of CS–UCS associations. (17 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

14.
Examined the ability of CS-evoked representations of flavored substances to modulate the conditioning of LiCl-based aversions to simultaneously presented flavors or odors. In Exps I–III, 156 thirsty Sprague-Dawley rats first received pairings of an auditory CS with a flavored-water UCS; they then received pairings of a compound stimulus with a toxin. Exp IV examined the potentiation of aversion conditioning to a novel odor using 32 Ss. In Exp I, conditioning of a flavor was partially overshadowed when it was presented in compound with a tone that had been previously paired with another flavor. Exp II replicated that result and also found that conditioning to a flavor was not overshadowed when the flavor was presented in compound with a tone that had been paired with that same flavored substance. In Exps III and IV, conditioning to an odor stimulus was potentiated when it was presented in compound with either a tone or another odor that had been previously paired with a flavor stimulus. Results suggest that evoked representations of stimuli may substitute for those events themselves in a variety of associative functions. (36 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

15.
20 overweight and 20 normal weight female undergraduates underwent habituation, classical conditioning, and extinction of the GSR. Overweight Ss were consistently more responsive to the CS (tone) during all 3 phases of the study and were somewhat more responsive to the UCS (shock). Rates of response attenuation and enhancement, however, were not different during any phase. Results are generally consistent with research which demonstrates that overweight Ss are more externally stimulus bound than normals. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

16.
The comparator hypothesis posits that conditioned responding is determined by a comparison at the time of testing between the associative strengths of the conditioned stimulus/stimuli (CS) and stimuli proximal to the CS at the time of conditioning. The hypothesis treats all associations as being excitatory and treats conditioned inhibition as the behavioral consequence of a CS that is less excitatory than its comparator stimuli. Conditioned lick suppression by rats was used to differentiate 4 possible sources of retarded responding to an inhibitory CS. These include habituation to the unconditioned stimulus/stimuli (UCS), latent inhibition to the CS, blocking of the CS-UCS association by the conditioning context, and enhanced excitatory associations to the comparator stimuli. Prior research has demonstrated the 1st 3 phenomena. Therefore, we employed parameters expected to highlight the 4th one—the comparator process. In Exp I, our negative contingency training produced a conditioned inhibitor that passed inhibitory summation and retardation tests. In Exp II we found transfer of retardation from an inhibitory CS to a novel stimulus when the location where retardation-test training occurred was excitatory. In Exp III, extinction of the conditioning context attenuated retardation regardless of whether extinction occurred before or after the CS-UCS pairings of the retardation test. Exp IV demonstrated that habituation to the UCS did not contribute to retardation in the present case. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

17.
Four experiments, with 136 male Sprague-Dawley rats, examined the properties of unconditioned analgesia elicited by electric footshock stimuli using UCS parameters typical of aversive conditioning paradigms. In all experiments, analgesia was inferred from the latency to paw lick in response to painful thermal stimulation in the hot-plate assay. In Exp I, Ss exposed to a 1-sec, 2-mA shock UCS showed significantly longer latencies to respond to painful thermal stimulation than nonshocked controls, whereas nonsignificant increases in response latencies were observed with 1-sec shock UCS of either 0.5 or 1.25 mA. In Exp II, Ss exposed to a 2-mA electric shock UCS showed systematic increases in latencies to respond to painful thermal stimulation as the duration of the shock was varied between 0.5 and 2 sec. Exp III showed that this form of shock-induced analgesia was of short temporal duration. Specifically, significant increases in latencies to respond to painful thermal stimulation occurred 30 but not 90 or 300 sec following exposure to shock. Exp IV demonstrated that this form of analgesia was unaffected by pretreatment with the opiate receptor antagonist naloxone HCl in ip dosages of 1, 5, 10, or 20 mg/kg. Finally, there was no evidence showing that environmental stimuli paired with shock presentations acquired the capacity to evoke analgesia as a conditioned response. Implications of shock-induced analgesia for the study of aversive conditioning and behavior are discussed. (26 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

18.
Examined conditioned suppression of photokinesis (CSPK) by the marine mollusc in 3 experiments. In each experiment, groups of Ss received light (conditioned stimulus, CS) paired with high-speed orbital rotation (unconditioned stimulus, UCS), light and rotation explicitly unpaired, or no exposure to these stimuli. 24 hrs after training, all Ss were tested for CSPK in the presence of the light. 50 CS–UCS pairings resulted in a marginal CSPK, whereas 100 and 150 pairings produced strong CSPK. In Exp 2, delay between CS onset and UCS onset was varied between 1 and 10 s. The 10-s interstimulus interval (ISI) did not support conditioning, whereas 1-s and 2-s ISIs were effective. In Exp 3, CS–UCS pairings in which the CS preceded the onset of the UCS and ended with the offset of the UCS evoked stronger CSPK than either a CS that preceded the UCS and ended with its onset or a CS that was paired in simultaneous compound with the UCS. CS–UCS contiguity and the forward ISI act additively to establish the CS–UCS association. No differences were observed between groups that were untreated and that received the CS and UCS unpaired. Similarities are noted in the temporal characteristics of associative learning in these Ss and vertebrate species. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

19.
20.
Examined the effects of prior pairings of conditioned stimulus/stimuli (CS)2 with the unconditioned stimulus/stimuli (UCS) on the nature of the associations formed in CS1?→?CS2?→?UCS serial compound conditioning, in 4 experiments with 72 male and 32 female albino rats. In Exps I and II, prior training of CS2 prevented the acquisition of stimulus–stimulus (S–S) associations between CS1 and stimulus features of CS2 but enhanced the acquisition of stimulus–response (S–R) associations between CS1 and the emotional conditioned response (CR) evoked by CS2. In Exps III and IV, the effects of CS2 pretraining were not due to CS2 training itself, but rather to its endowing CS2 with the ability to evoked a strong CR during the early stages of serial compound conditioning. In Exp III, suppression of the CR to a pretrained CS2 during serial compound conditioning permitted the establishment of S–S associations. In Exp IV, the induction of a CR in the presence of an untrained CS2 during serial compound conditioning prevented the acquisition of S–S associations. (31 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

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