Two temporal parameters of food postponement

Rats were trained to press a lever under schedules of food postponement. In the absence of lever presses, food was delivered periodically (food-food interval). Responses initiated a second interval (response-food interval) that was reset by each additional response. Performance was first studied at different response-food intervals with the food-food interval fixed at 30 or 60 sec, or 10 min. Response-food intervals were examined in ascending order and then recovery was studied at shorter intervals. Finally, the food-food interval was manipulated with response-food interval fixed at 30 sec. At food-food intervals of 30 and 60 sec, responding first increased and then decreased as the response-food interval increased. At the 10-min food-food interval, responding decreased with increasing response-food interval. In general, very low rates of responding occurred when the response-food interval was 60 sec or more and when it equalled or exceeded the food-food interval. However, responding was maintained in one animal when the food-food interval was decreased from 120 to 15 sec with the response-food interval at 30 sec. Results, in terms of several dependent variables, are compared with data on shock avoidance. Effects of response-independent and response-produced food and shock are discussed.     

不同时距加工机制的比较:来自ERP的证据(Ⅰ)

采用事件相关电位的方法分析了不同时距加工机制的差异。实验采用时间两分任务,要求被试形成短(400ms)和长(1600ms)的时间判断标准,然后对7个刺激系列进行短、长的判断。结果表明时间知觉过程可以诱发出一种类似于CNV的慢性负波。对于400ms的短时距加工存在显著的半球效应,右半球的波幅显著高于左半球。1600ms的时距加工没有表现出明显的半球效应。不同时距的加工存在显著的差异。1600ms比400ms加工诱发出更大的CNV波幅。     

An interval size illusion: the influence of timbre on the perceived size of melodic intervals

In four experiments, we investigated the influence of timbre on perceived interval size. In Experiment 1, musically untrained participants heard two successive tones and rated the pitch distance between them. Tones were separated by six or seven semitones and varied in timbre. Pitch changes were accompanied by a congruent timbre change (e.g., ascending interval involving a shift from a dull to a bright timbre), an incongruent timbre change (e.g., ascending interval involving a shift from a bright to a dull timbre), or no timbre change. Ratings of interval size were strongly influenced by timbre. The six-semitone interval with a congruent timbre change was perceived to be larger than the seven-semitone interval with an incongruent timbre change (interval illusion). Experiment 2 revealed similar effects for musically trained participants. In Experiment 3, participants compared the size of two intervals presented one after the other. Effects of timbre were again observed, including evidence of an interval illusion. Experiment 4 confirmed that timbre manipulations did not distort the perceived pitch of tones. Changes in timbre can expand or contract the perceived size of intervals without distorting individual pitches. We discuss processes underlying interval size perception and their relation to pitch perception mechanisms.     

Shortening of subjective tone intervals followed by repetitive tone stimuli

Accumulated evidence shows that a subjective time interval is lengthened by preceding or concurrent presentation of flickers or repetitive tone stimuli that have been hypothesized to increase the frequency of pulse generation by a brain pacemaker. In the present study, we presented a series of repetitive tone stimuli after an interval that started and ended with tone markers. We found that subjective perception of the preceding interval was not lengthened but shortened by the tone stimuli that followed the interval. The perceived duration decreased as the frequency of the repetitive tone stimuli increased. The effect disappeared when the repetitive tone stimuli were delivered with a delay of 500 msec after the test interval or when continuous sound was delivered instead of delivering a rapid series of tones. On the basis of the results, we propose that the pulse count accumulated during a test interval was normalized by the clock frequency just after the test interval in a postdictive manner.     

Time-shrinking,its propagation,and Gestalt principles

When a relatively short empty time interval is preceded by an even shorter one, its duration can be underestimated remarkably. This phenomenon, called time-shrinking, has been investigated with patterns consisting of two time intervals. In five experiments, we investigated whether underestimation of the last interval would occur when it was preceded by two time intervals. Significant underestimations of the last interval occurred in some of those patterns. The influence of the second preceding interval was dominant, but in some patterns, the first preceding interval could shrink the subjective duration of the last time interval directly. The first interval could also affect perception of the duration of the last one indirectly by shrinking the second interval, as a result of which the latter either shrank the last interval more strongly or became too short to shrink it. There were two types of temporal patterns in which the perceived duration of the last interval could not be explained by time-shrinking or its propagation through the pattern. It seemed plausible that auditory Gestalt principles invoked strong figural organizations in these patterns, which rendered the time-shrinking mechanism inoperative.     

The response-shock-shock-shock interval and unsignalled avoidance in goldfish

Goldfish were trained to swim back and forth in a shuttle tank to avoid unsignalled shocks. The response-shock interval and the shock-shock interval were always of equal duration; both were either 15, 30, 45, or 60 sec. Response rates varied inversely with response-shock–shock-shock interval duration, as has been found with rats. Percentage of shocks avoided was somewhat lower at the 15 sec response-shock–shock-shock interval, but otherwise did not vary systematically with changes in the interval. As the response-shock–shock-shock interval increased, the fish made increasingly more responses than necessary to avoid all shocks. Interresponse-time distributions showed that response probability rose to a maximum at about 15 to 25 sec after a response, regardless of the response-shock–shock-shock interval. Thus, at the longer intervals the fish were responding too early in the response-shock–shock-shock interval to minimize response rates.     

Concurrent variable‐interval variable‐ratio schedules in a dynamic choice environment

Most studies of operant choice have focused on presenting subjects with a fixed pair of schedules across many experimental sessions. Using these methods, studies of concurrent variable‐ interval variable‐ratio schedules helped to evaluate theories of choice. More recently, a growing literature has focused on dynamic choice behavior. Those dynamic choice studies have analyzed behavior on a number of different time scales using concurrent variable‐interval schedules. Following the dynamic choice approach, the present experiment examined performance on concurrent variable‐interval variable‐ratio schedules in a rapidly changing environment. Our objectives were to compare performance on concurrent variable‐interval variable‐ratio schedules with extant data on concurrent variable‐interval variable‐interval schedules using a dynamic choice procedure and to extend earlier work on concurrent variable‐interval variable‐ratio schedules. We analyzed performances at different time scales, finding strong similarities between concurrent variable‐interval variable‐interval and concurrent variable‐interval variable‐ ratio performance within dynamic choice procedures. Time‐based measures revealed almost identical performance in the two procedures compared with response‐based measures, supporting the view that choice is best understood as time allocation. Performance at the smaller time scale of visits accorded with the tendency seen in earlier research toward developing a pattern of strong preference for and long visits to the richer alternative paired with brief “samples” at the leaner alternative (“fix and sample”).     

Perception and production of brief durations: beat-based versus interval-based timing

Two experiments examined whether timing of short intervals is beat- or interval-based. In Experiment 1, subjects heard a sequence of standard tones followed by 2 test tones; they compared the interval between test tones to the interval between the standards. If optimal precision required beat-based timing, performance should be best in blocks in which the interval between standard and test reliably matched the standard interval. No such effect was observed. In Experiment 2, subjects heard 2 test tones and reproduced the intertone interval by producing 2 keypress responses. Entrainment to the beat was apparent: First-response latency clustered around the standard interval and was positively correlated with the produced interval. However, responses occurring on or near the beat showed no better temporal fidelity than off-beat responses. One plausible interpretation of these findings is that the brain always times brief intervals with an interval timer; however, this timer can be used in a cyclic fashion to trigger rhythmic responses.     

Extinction of Sidman avoidance behavior

Extinction of Sidman avoidance behavior by eliminating the noxious stimulus was studied in Sprague-Dawley rats with bar-pressing as the response. Each of three subjects was trained and extinguished on each of the following schedules in a different order: nondiscriminated, response-shock interval = 20 sec, shock-shock interval = 5 sec; nondiscriminated, response-shock interval = 40 sec, shock-shock interval = 5 sec; discriminated, response-white noise interval = 15 sec, noise-shock interval = 5 sec, shock-shock interval = 5 sec. Less than one 4-hr session was required for extinction for all procedures. When a warning stimulus was present, resistance to extinction increased. Subjects did not, however, respond to avoid the signal. Only small differences in extinction were found after training on different schedules with no warning signal.     

Fixed interval schedules and delay of reinforcement

In a fixed interval schedule of reinforcement the only responses to be reinforced are those made when a certain time interval has elapsed since the previous reinforcement. The behaviour of three rats on such a schedule was compared with their behaviour on a schedule where a response made at any time during the interval was reinforced by setting up a reward which was delivered when the interval had elapsed. Response rates were higher in the ordinary fixed interval schedule than in its modified version, and it is argued that this rules out attempts to explain the maintenance of fixed interval performance by delayed reinforcement. Despite the clear difference in response rates, there was considerable similarity between the post-reinforcement pauses developed in the two schedules, and this suggests that pausing is influenced more by temporal than by response contingencies.     

Frequency thresholds for two-flash flicker and critical flicker: Why they differ

The minimum interval detectable between two successive flashes is longer than the minimum interval detectable when many flashes are viewed. The probability summation hypothesis is suggested to explain the difference. For a given flash duration, the minimum interval detectable decreases as a function of the number of flashes, n, until n equals about 8 or 10; further increases in n cause no further changes in this interval. Of the total decrease in the interval, from n=2 to n=99, about 90% is explained by the probability summation hypothesis.     

Accuracy of observational data with whole interval,partial interval,and momentary time-sampling recording techniques

The purpose of the study was to compare the accuracies obtained from whole interval, partial interval, and momentary time-sample recording procedures. Two types of accuracies were defined. Between-methods accuracy is the degree to which an observer using a particular recording method agrees with a standard using a continuous recording method. Within-methods accuracy is the degree to which an observer and a standard agree when both use the same recording method. Fifty-four undergraduate students viewed a videotape of a woman twisting her hair and recorded the occurrence or nonoccurrence of the behavior using one of the three recording methods. Tapes were divided into segments with low, intermediate, and high rates of behavior. Partial and whole interval recording obtained poorer between-methods accuracies than momentary time sampling. Results showed that whole interval and momentary time-sampling procedures yielded higher within-method accuracies than partial interval recording. Thus, momentary time-sampling recording provided the advantages of both greater representativeness and as few or fewer observer errors than whole or partial interval recording procedures. Use of the interval recording methods by researchers must be justifiable within this framework.     

Retention of Conditioned Inhibition Produced by Extinction

Rats in a flavor aversion procedure were used to examine the extent to which an extinguished CS can pass a retardation and summation test for conditioned inhibition after either a short or a long retention interval. Rats were given a single pairing of a flavored solution with LiCl, and then received a large number of CS-alone extinction trials. Following extinction, some subjects received a 3-week retention interval following extinction while others did not. Extinction produced evidence of conditioned inhibition on both tests when a short retention interval occurred following extinction. However, conditioned inhibition was attenuated by the long retention interval when assessed with a retardation test, but no effect of the long retention interval was observed when inhibition was evaluated with a summation test.     

Application of Sequential Interval Estimation to Adaptive Mastery Testing

In this paper, we apply sequential one-sided confidence interval estimation procedures with β-protection to adaptive mastery testing. The procedures of fixed-width and fixed proportional accuracy confidence interval estimation can be viewed as extensions of one-sided confidence interval procedures. It can be shown that the adaptive mastery testing procedure based on a one-sided confidence interval with β-protection is more efficient in terms of test length than a testing procedure based on a two-sided/fixed-width confidence interval. Some simulation studies applying the one-sided confidence interval procedure and its extensions mentioned above to adaptive mastery testing are conducted. For the purpose of comparison, we also have a numerical study of adaptive mastery testing based on Wald's sequential probability ratio test. The comparison of their performances is based on the correct classification probability, averages of test length, as well as the width of the “indifference regions.” From these empirical results, we found that applying the one-sided confidence interval procedure to adaptive mastery testing is very promising.     

Memory and the experience of duration in retrospect

Two experiments investigated the relationship between long-term memory for events occurring during an interval and the experience of duration of the interval in retrospect. In both, Ss attended to a sequence consisting of a standard, an experimental, and a second standard interval. Then unexpected comparative duration and memory judgments were requested. In Experiment I, either 30 or 60 unrelated words occurred during the 180-see experimental interval. When more words had occurred, judgments of duration of the experimental interval, judgments of number of words presented, and number of words recognized all increased, but free recall of words was unaffected. In Experiment II, 80 categorized words occurred during the 160-see experimental interval, with category instances in either blocked or random order. When words were blocked by category, judgments of duration of the experimental interval, free recall, and recognition all increased, but judgments of number of words were unaffected. Results were discussed in terms of Ornstein’s (1969) “storage size” hypothesis.     

Sensorimotor synchronization: Motor responses to regular auditory patterns

Subjects (N = 32) were asked to synchronize a motor response with tones in auditory patterns. These patterns were created from six tones and six intertone intervals of equal duration. The pitch of the first tone differed from the others. It was found that subjects used three types of timing in their motor response: (1) the first intertone interval was prolonged and the second interval was shortened, (2) the second intertone interval was prolonged and the first interval was shortened, and/or (3) the first interval and the second interval were of approximately the same length. The prolongation of the fifth interval was observed during all three types of timing. The results are explained using the concept of suprasegmental control of timing, which explains a prolongation of intervals at critical control point of the patterns. The occurrence of three different strategies of timing is discussed in connection with similar principles in musical performance.     

Some empirical justification for a modest proposal regarding data acquisition via intermittent direct observation

Computer simulations of behavior and event records of a child's visual fixation on an adult person were generated and sampled using a modified time sampling procedure. The modified approach required making two independent scoring judgments per observation interval: if the behavior was initiated within the interval, the interval was scored; if the behavior was ongoing precisely at the end of the interval, the interval was again scored. The results showed that the within-interval and end-of-interval scores yielded, respectively, estimates of behavioral frequency and duration. The accuracy of the estimates was a function of the number of observations. Several field studies demonstrated high agreement among observers who employed the measurement system.     

Manipulation of CS-US conditional probability and of the US-US trace interval on conditioning to the CS and to a background stimulus in a CER situation

Two experiments examined the relationship between conditioning to the CS and background using a novel CER paradigm, in which a long background stimulus played the role of more conventional contextual cues. Experiment 1 manipulated the probability of US occurrence given the CS (p(US/CS)). Conditioning to the background was not a monotonically decreasing function of p(US/CS) at all shock intensities, and conditioning to the CS was remarkably insensitive to the value of p(US/CS) when assessed off the baseline. Experiment 2 manipulated the trace interval between the CS and US. Although conditioning to the CS decreased as the trace interval increased, conditioning to the background was dependent upon whether it served as the interstimulus interval (ISI; interval between the CS and US) or intertrial interval (ITI; interval between CS-US pairs) stimulus. Conditioning to the ISI background decreased as the trace interval increased, but conditioning to the ITI background at first increased, but then decreased as the trace interval was further increased. These results are discussed with respect to the adequacy of contemporary models of conditioning.     

Place avoidance learning and memory in a jumping spider

Using a conditioned passive place avoidance paradigm, we investigated the relative importance of three experimental parameters on learning and memory in a salticid, Servaea incana. Spiders encountered an aversive electric shock stimulus paired with one side of a two-sided arena. Our three parameters were the ecological relevance of the visual stimulus, the time interval between trials and the time interval before test. We paired electric shock with either a black or white visual stimulus, as prior studies in our laboratory have demonstrated that S. incana prefer dark ‘safe’ regions to light ones. We additionally evaluated the influence of two temporal features (time interval between trials and time interval before test) on learning and memory. Spiders exposed to the shock stimulus learned to associate shock with the visual background cue, but the extent to which they did so was dependent on which visual stimulus was present and the time interval between trials. Spiders trained with a long interval between trials (24 h) maintained performance throughout training, whereas spiders trained with a short interval (10 min) maintained performance only when the safe side was black. When the safe side was white, performance worsened steadily over time. There was no difference between spiders tested after a short (10 min) or long (24 h) interval before test. These results suggest that the ecological relevance of the stimuli used and the duration of the interval between trials can influence learning and memory in jumping spiders.     

Retention interval and intertrial interval in a serial learning or delayed discrimination task

In each of four experiments, rats were provided with the same three-event decreasing series (18-1-0) of 0.045-g food pellets in a runway. Tracking, running fast to 18 pellets and running slow to 1 and 0 pellets, was investigated as a function of the temporal interval elapsing between the events of the series (the retention interval), shifts in retention interval, and number of trials each day (or the intertrial interval), a trial being defined as presentation of each of the three events of the series. Neither retention interval, which varied from 15 s to 30 min in various investigations, nor shifts in retention interval affected tracking when only one trial was given each day. But when more than one daily trial was given, tracking was acquired more slowly and was disrupted by a shift in retention interval from 15 s to 5 min. Tracking was also disrupted by a shift from one to two trials each day. These results indicate that when given one 18-1-0 trial each day, the rat partitions events on a first-event/subsequent-event basis; that little forgetting occurs even at long retention intervals; that somewhat different memories signal events when one or more than one 18-1-0 trial occurs each day; and that retention interval deficits can arise owing to the same or similar memories' signaling different events. The results described limit the generality of three hypotheses suggested in two recent investigations: that as retention interval increases, rats find it increasingly difficult to remember and utilize serial position cues; that tracking in serial tasks is not influenced by number of trials each day; and that there are specific stimuli associated with each retention interval which, when changed, necessarily disrupt performance.