Temporal context in concurrent chains: I. Terminal-link duration

Two experiments are reported in which the ratio of the average times spent in the terminal and initial links (Tt/Ti) in concurrent chains was varied. In Experiment 1, pigeons responded in a three-component procedure in which terminal-link variable-interval schedules were in constant ratio, but their average duration increased across components by a factor of two. The log initial-link response ratio was a negatively accelerated function of Tt/Ti. Overall, the data were well described by Grace's (1994) contextual choice model (CCM) with temporal context represented as (Tt/Ti)k or 2Tt/(Tt + Ti), and by Mazur's (2001) hyperbolic value-added model (HVA), with each model accounting for approximately 93% of the variance. In Experiment 2, fixed-parameter predictions for each model were generated, based on the data from Experiment 1, for conditions in which Tt/Ti was varied over a more extreme range. Data were consistent with the predictions of CCM with temporal context represented as 2Tt/(Tt + Ti) and to a lesser extent as (Tt/Ti)k, but not with HVA. Overall, these results suggest that preference increases as a hyperbolic function of Tt/Ti when terminal-link duration is increased relative to initial-link duration, with the terminal-link schedule ratio held constant.     

Leaving patches: effects of economy, deprivation, and session duration

Three pigeons pecked keys for food reinforcers in a laboratory analogue of foraging in patches. Half the patches contained food (were prey patches). In prey patches, pecks to one key occasionally produced a reinforcer, followed by a fixed travel time and then the start of a new patch. Pecks to another key were exit responses, and immediately produced travel time and then a new patch. Travel time was varied from 0.25 to 16 s at each of three session durations: 1, 4, and 23.5 hr. This part of the experiment arranged a closed economy, in that the only source of food was reinforcers obtained in prey patches. In another part, food deprivation was manipulated by varying postsession feeding so as to maintain the subjects' body weights at percentages ranging from 85% to 95% of their ad lib weights, in 1-hr sessions with a travel time of 12 s. This was an open economy. Patch residence time, defined as the time between the start of a patch and an exit response, increased with increasing travel time, and consistently exceeded times predicted by an optimal foraging model, supporting previously published results. However, residence times also increased with increasing session duration and, in longer sessions, consistently exceeded previously reported residence times in comparable open-economy conditions. Residence times were not systematically affected by deprivation levels. In sum, the results show that the long residence times obtained in long closed-economy sessions should probably be attributed to session duration rather than to economy or deprivation. This conclusion is hard to reconcile with previous interpretations of longer-than-optimal residence times but is consistent with, in economic terms, a predicted shift in consumption towards a preferred commodity when income is increased.     

Choice, contingency discrimination, and foraging theory

Four pigeons were trained on eight or nine pairs of independent concurrent variable-interval schedules. The range of reinforcement ratios included extreme ratios (up to 532 to 1). Large samples of stable performance were gathered. Contrary to the findings of Davison and Jones (1995), the generalized matching law described choice more accurately than a contingency-discriminability model. Taking small samples (5 to 10 sessions) and applying a more liberal stability criterion used by Davison and Jones only increased the unsystematic variance in the data and in estimates of generalized-matching-law sensitivity. Because changing to dependent scheduling and inserting a changeover delay had no systematic effect, the deviations from generalized matching reported by Davison and Jones probably arose from imperfectly discriminated stimuli. Analysis of visits revealed that visits to the nonpreferred alternative were brief and approximately constant. When choice between the preferred (rich) and nonpreferred (lean) alternatives, regardless of position, was analyzed according to the generalized matching law, sensitivities approximated 1.0, with bias in favor of the lean alternative. This bias, which arose from an excessive frequency of visits to the lean alternative, explains undermatching as the result of fitting one line to a choice relation that consists of two displaced lines, both with a slope of 1.0. The pattern of deviation from the generalized matching line confirmed this account. The findings suggest an alternative analysis of choice that focuses on probability of visiting the lean alternative as the dependent variable. This probability was directly proportional to ratio of reinforcement. Matching, undermatching, and overmatching may all be explained by a view of concurrent performance based on foraging theory, in which responding occurs primarily at the rich alternative and is occasionally interrupted by brief visits to the lean alternative.     

时点,时距和时序信息加工之间相关性研究

本研究分为两个实验,分别采用预期式和回溯式范型,探讨时距、时序和时点三者之间信息加工的相关性,结果发现：同一时间经历,时距估计与时序判断随注意参与程度的增加,由负相关趋势向正相关变化;时距估计与时点离散度可能呈正相关趋势;时序判断与时点离散度随注意参与程度的增加,由负相关趋势向正相关变化。     

人是怎样与世界统一的——一个关于细胞信息跨膜传递特异性的假说

本文在讨论有限和无限的对立统一规律在抗原和抗体产生机制中的体现的基础上,提出关于细胞信息跨膜传递特异性机制的假说：第一信使可能由有限的基本单位构成,其信息的特异性可能通过有限的信息中介的组合来得以体现,效应部位也可能因具有特定的信息中介结合位点的组合而产生特异的细胞效应。本文最后为这一假说的证实提出展望。     

学前儿童对短时时距的区分及其认知策略

本研究以令儿童比较时距长短为手段进一步探查学前（５、６岁）儿童对短时时距的认知过程,挖掘幼儿的认知潜力。研究结果表明：１）学前５、６岁儿童已能区分只有几秒钟差异的短时时距;２）６岁儿童已能使用时间标尺测量时间,５岁儿童已有潜力把时间看成是可以计数的维量;３）两时距的时间差别大小是影响儿童认知成绩的主要因素之一。     

Decision rules and signal detectability in a reinforcement-density discrimination

Two probabilistic schedules of reinforcement, one richer in reinforcement, the other leaner, were overlapping stimuli to be discriminated in a choice situation. One of two schedules was in effect for 12 seconds. Then, during a 6-second choice period, the first left-key peck was reinforced if the richer schedule had been in effect, and the first right-key peck was reinforced if the leaner schedule had been in effect. The two schedule stimuli may be viewed as two binomial distributions of the number of reinforcement opportunities. Each schedule yielded different frequencies of 16 substimuli. Each substimulus had a particular type of outcome pattern for the 12 seconds during which a schedule was in effect, and consisted of four consecutive light-cued 3-second T-cycles, each having 0 or 1 reinforced center-key pecks. Substimuli therefore contained 0 to 4 reinforcers. On any 3-second cycle, the first center-key peck darkened that key and was reinforced with probability .75 or .25 in the richer or leaner schedules, respectively. In terms of the theory of signal detection, detectability neared the maximum possible d′ for all four pigeons. Left-key peck probability increased when number of reinforcers in a substimulus increased, when these occurred closer to choice, or when pellets were larger for correct left-key pecks than for correct right-key pecks. Averaged over different temporal patterns of reinforcement in a substimulus, substimuli with the same number of reinforcers produced choice probabilities that matched relative expected payoff rather than maximized one alternative.     

Comparison of yes-no and latency measures of auditory intensity discrimination.

Rats discriminated auditory intensity differences of sinusoids at 3.0 kilohertz in a go/no-go signal detection procedure. Responses to the signal (hits) were reinforced with electrical brain stimulation, and misses produced a brief timeout. On intermixed noise trials, withholding of responses (correct rejections) was reinforced, and false alarms produced the time-out. In two test conditions, the signal was either the louder (100 decibels) or softer (90, 93, 96, or 99 decibels) of the pair of intensities presented within a set of trials. Each animal was first trained with signal value louder or softer, and reversed for the second condition so that the former noise value served as signal. Hits showed shorter latencies than false alarms, regardless of the relative intensity of signal and noise, and the magnitude of differentiation was proportional to signal-noise separation. Both hits and false alarms showed longer latencies as the discrimination became more difficult. Isosensitivity contours derived from the latencies showed close similarity across conditions; in comparison, the yes-no measure of detectability, d', showed greater variability. The similarity of latency differentiation across louder and softer signal conditions supports a detection model in which the observer's judgment is controlled by the distance of sensory effect from criterion on each trial, as opposed to the loudness of the tones per se.     

Reinforcement contingencies as discriminative stimuli: II. Effects of changes in stimulus probability.

Three pigeons were trained on a matching procedure involving a sample component and a choice component. Responding in the sample component, according to either a differential-reinforcement-of-low-rate schedule on some trials or a differential-reinforcement-of-other-behavior schedule on other trials, produced access to the choice component in which each of two keys was illuminated with a unique color. The correct choice response was defined by the contingency that was met to produce the choice. The food hopper operated for 1.5 seconds following an appropriate sample response and for 3 seconds following a correct choice response. A signal-detection analysis showed that variations in the probability of presentation of the different contingencies systematically affected response bias but not sensitivity to the contingencies as stimuli. Substitution of a blackout for food at the end of the sample component did not differentially affect performance, but elimination of the delay between sample and choice components generally increased the sensitivity measure. The findings suggest a role for reinforcement contingency discrimination in schedule-controlled responding.     

Conditioned reinforcement as a function of duration of stimulus

Pigeons were provided with three keys. Pecking the center key produced grain on a schedule that alternated at unpredictable times between a variable-interval component and extinction. On concurrent variable-interval schedules, pecking either side key produced a stimulus associated with the variable-interval component on the center key provided that said schedule was currently in effect. The independent variable was the length of time this stimulus remained on the keys. Pecking one side key produced the stimulus for 27 seconds, whereas the duration produced by pecking the other key varied for successive blocks of sessions. For the first four birds, the values tested were 3, 9, 27, and 81 seconds. For the second group, numbering three birds, the values tested were 1, 3, 9, and 27 seconds. The dependent variable was the proportion of total side key pecks that occurred on the variable key. For all birds, the function was positive in slope and negative in acceleration. This finding supports a formulation that ascribes the maintenance of observing responses in a normal setting to the fact that the subject exposes itself to the positive discriminative stimulus for a longer mean duration than it does to the negative stimulus.