Reciprocal heuristics: A discussion of the relationship of the study of learned behavior in laboratory and field

At the turn of the century, the initiators of laboratory study of animal learning advocated two very different approaches to the subject matter. Willard Small favored the investigation of learning in ecological settings appropriate to individual species. E. L. Thorndike treated the process of association formation in animals as a general one, best studied in situations distant from those to which subject species were adapted. The latter view dominated laboratory study of animal learning for 80 years. The consequent absence of ecological content from laboratory investigations of animal learning, together with recent expansion in knowledge of the behavior of free-living animals, has created opportunities for ecologically sound investigations of animal learning of the type first advocated by Small. Studies of taste-aversion learning, although introducing evolutionary issues into the study of animal learning, do not exemplify such an approach. Integration of field and laboratory studies of behavioral plasticity in animals requires a change in the methods used to select phenomena for analysis. Such integration does not often lead to identification of the behavioral processes underlying the development of particular behaviors observed in nature. Rather, its results are an increase in the variety of learning processes investigated in laboratory settings and enhanced understanding of the behavioral capacities of subject species.     

On the failure of transfer of control from separately conducted Pavlovian conditioning to free-operant avoidance conditioning in rats

In Experiment 1, presentation of a tone previously correlated with foot shock produced an increase in the rate of rats' foot-shock avoidance responding, while presentation of a tone previously correlated with tail shock had no reliable effect on the rate of foot-shock avoidance responding. In Experiment 2, a tone correlated with tail shock elicited heart-rate conditioned responses, but had no reliable effect on the rate of subsequent foot-shock avoidance responding. In Experiment 3, presentation of a tone previously correlated with foot shock, and a tone previously correlated with tail shock in separate groups produced increases in the rate of tail-shock avoidance responding. In Experiment 4, a tone correlated with tail shock in one setting accelerated tail-shock avoidance responding in a second setting. Interaction between US and negative reinforcer modifiability by skeletal responding may contribute to the pattern of results obtained.     

Central vision in the newborn

Newborns' fixations on a 4° dot were longer than their fixations on the comparable part of a blank field. This suggests newborns can detect a stimulus with the fovea or with some part of the retina near the fovea.     

Contiguity and contingency in the acquisition and maintenance of an operant

Three experiments compared the effects of nondifferential and differential reinforcement of response location on a circular dimension. Rats were required to operate a vertical joystick to produce food. When food was delivered immediately after responses, but independent of response location, the spatial concentration of responding was low and no progressive changes were observed. Traditional and percentile schedules of differential reinforcement for response location produced highly reliable acquisition of spatially concentrated responding. Once concentrated responding had been established, nondifferential reinforcement was sufficient to maintain it in some subjects. Since only the differential reinforcement schedules established a contingency with respect to response location, it was concluded that this relationship was necessary for acquisition, but that response-reinforcer contiguity may be sufficient for maintenance. This conclusion is consistent with the view that operant conditioning is a contiguity-based process, but that contingencies are required to produce reliable contiguity between reinforcers and particular responses.     

Imagery and associative memory in children

Second and sixth graders, ages 7–8 and 11–12, respectively, were presented with lists of pairs of nouns. They were asked to represent each pair in memory as a single interactive image, as two separate images, or by a control procedure. After presentation of the pairs, the children were tested either by cued or noncued recall. The difference between the interaction condition and the other conditions appeared in recall measures which reflect pairwise organization in memory (cued recall, pair recall, conditional recall probabilities, and χ²) to a much greater extent than in measures of individual item recall. The results were interpreted as supporting an imagery-organization hypothesis.     

Extinction of morphine analgesic tolerance

It has been suggested that the analgesic effect of morphine becomes attenuated over the course of successive administrations by a conditional, compensatory, hyperalgesic response elicited by the administration procedure, thus accounting (in part) for analgesic tolerance. On the basis of this associative model of tolerance, it would be predicted that established tolerance would be extinguished by placebo sessions. In experiments of apparently similar design (but conducted by different experimenters in different laboratories), data both confirming and refuting this prediction have previously been published. The present experiment, conducted jointly by the experimenters who reported the divergent findings, was designed to determine the reasons for the different results. It was found that placebo sessions do consistently attenuate morphine analgesic tolerance. Such extinction is not limited to the experimenter, drug preparation, rat strain, or apparatus used in the original, successful demonstration of the phenomenon, but rather is also demonstrable under conditions similar to those used in subsequent experiments which failed to demonstrate extinction of tolerance. Results of the present experiment suggest that the failures to demonstrate extinction of tolerance were attributable to insufficient extinction training.     

Overshadowing and blocking of the orientation-contingent color aftereffect: Evidence for a conditioning mechanism

Orientation-contingent color aftereffects have been interpreted by nonassociative mechanisms (adaptation of neural units that are both color and orientation specific) and by associative mechanisms (conditioning resulting from the pairing of pattern and hue). To evaluate associative accounts, contingent aftereffects were induced by exposing subjects to compound chromatic grid patterns consisting of two component gratings: one was horizontal or vertical, and the other a left- or right-learning diagonal. The ability of a component grating to elicit a color aftereffect depended on the relative salience and the aftereffect training history of the grating components. That is, orientation-contingent color aftereffects, like other conditional responses, display overshadowing and blocking. The results suggest that conditioning contributes to these aftereffects.     

The scanning of compound figures by young infants

We studied infants' scanning of two compound stimuli, in each case by presenting features inside a frame, the frame alone, and the features alone. One stimulus was composed of squares and was like that studied by P. Salapatek (in L. Cohen & P. Salapatek (Eds.), New York: Academic Press, 1975); the other was a schematic face. Newborns and 1-month-olds looked at the small square when it was presented alone, but rarely looked at it when it was framed by the larger square. In contrast, 2-month-olds looked at the small square for long periods whether or not it was framed. However, when newborns and 1-month-olds were shown a schematic face, they looked at its internal features at least half the time. Thus, young infants show no external bias when scanning a schematic face.     

An organizational analysis of the form class effect

The paper reports eight experiments concerning the form class effect. If verb connectives enhance organization between pairs of nouns more than do conjunction connectives, then (a) the form class effect should obtain in cued but not free recall, (b) interactive imagery instructions should raise performance with conjunctions, removing the effect, (c) separation imagery instructions should reduce performance with verbs, removing the effect, and (d) prepositions implying spatial contact should be superior as mediators for cued recall compared with less suggestive prepositions. The results of the experiments confirm the predictions, except that grade 3 children do not perform as expected with the instructional variables.     

Newborns' central vision: Whole or hole?

We studied visual detection in 150 infants, 1- to 7-days old, by presenting single lines varying in width and location. We found that newborns detected a line only 8′ wide in the central visual field. Peripherally, they appeared to detect lines of 33′, 33′, and 1°6′ at 10°, 20°, and 30°, respectively. Thus, both the central retina and the peripheral retina appear to function at birth.     

Operant baseline procedures suppress infant social behavior

Two groups of six 3-month-old infants participated in a study which contained four consecutive 2-min periods. During Periods 2 and 4 both groups received adult social stimulation on the same prearranged schedule. The treatments during Periods 1 and 3 differed between the two groups; no adult was present for the A-S group, while the B-S group received the typical operant baseline (unresponsive adult treatment) for these two periods. Social stimulation caused a significant increase in vocal rate from the preceding control period for both groups. Infants in the A-S group vocalized at the same rate during the two periods in which the adult was absent and at similar rates during the two stimulation periods. For infants in the B-S group, baseline procedures suppressed vocal rates and did not provide a neutral or operant level of responding with which the effects of social conditioning could be compared.     

Spatial memory in the rat on a hierarchical maze

Rats were trained and tested on a hierarchical radial maze, which consisted of eight primary alleys radiating from a central platform and three secondary alleys which branched off the end of each primary alley. In four experiments, rats in groups 1, 2, and 3 were tested on maze configurations consisting of one, two, or three secondary alleys, respectively, at the end of each primary alley. In Experiment 1, each group was trained to collect food pellets in the secondary alleys. By the end of training, rats in each group collected all pellets efficiently, with little repetition of entrances into either primary or secondary alleys. In Experiments 2 and 3, tests were carried out which required retention of entrances into secondary alleys, as well as primary alleys. Two trials were run in succession, with selected secondary alleys blocked on trial 1 but open and baited with food on trial 2. Animals in groups 2 and 3 showed very accurate retention of blocked secondary alleys, regardless of variation in pattern and number of alleys blocked. A fourth experiment controlled for the possible use of food cues in Experiments 2 and 3 by rebaiting all secondary alleys between trials 1 and 2. Subjects continued to choose previously blocked alleys on trial 2, thus demonstrating that choice of blocked alleys was based on memory and not on a tendency to approach visual or olfactory food cues. Several findings of these experiments suggest that memories for primary and secondary alley choices are encoded and stored within separate memory systems. Possible coding mechanisms for these systems are discussed with reference to a process of cognitive mapping.     

Remembrance of places lasts: Proactive inhibition and patterns of choice in rat spatial memory

A series of experiments was carried out to evaluate the notion that rats given a sequence of massed daily trials on the radial maze reset working memory at the end of each trial by deleting its contents. Although curves presented by D. S. Olton [Scientific American, 1977, 236, 82–98; In S. H. Hulse, H. Fowler, & W. K. Honig (Eds.), Cognitive processes in animal behavior, Hillsdale, N.J.: Erlbaum, 1978] show that rats return to errorless performance at the beginning of each trial after the first, the fact that accuracy falls less rapidly over choices on Trial 1 than on subsequent trials suggests a proactive inhibition (PI) effect. In Experiment 1, Olton's findings were replicated, and a PI effect was observed on Days 1–2 of testing. On Days 3–5, overall accuracy improved significantly and was associated with the development of a strong tendency for rats to enter adjacent alleys, which became particularly marked on the final trials of a day's testing. In order to prevent rats from achieving accurate performance by using an adjacent alleys pattern, a procedure was used in Experiment 2 which involved initial forced random choices followed by a retention test consisting of free choices. Repeated daily trials with this procedure yielded a significant PI effect, which was more marked at a 60-sec delay than at a 0-sec delay. Experiments 3 and 4 showed this PI effect to be robust and resistant to manipulations designed to produce release from PI. Both the PI effect and a strong tendency found in Experiment 1 for animals to avoid on the initial choices of Trial n those alleys most recently entered on Trial n?1 argue that rats do not reset working memory between trials.     

Sign-tracking in aversive conditioning

Two experiments were conducted to determine if rats tend to avoid contact with a stimulus that signals the occurrence of shock and contact a stimulus that signals the nonoccurrence of shock. The conditioned stimulus was a 60-sec platform presentation, and the unconditioned stimulus was a 2-sec inescapable shock. In each experiment, the emphasis was on two types of Pavlovian pairings: forward pairing in which each platform presentation was followed by shock, and backward pairing in which each platform presentation was preceded by shock and followed by a lengthy shock-free interval. Experiment 1 showed that in comparison with Random and CS-only procedures, the backward procedure produced a significant increase in approach and contact with the platform, but the forward procedure failed to produce a significant decrease in contact with the platform. Experiment 2, in which all groups were roughly equated for baseline levels of platform preference, demonstrated strong effects of both forward and backward conditioning. The experiments provide evidence for an aversive sign-tracking system in which animals' tendencies to withdraw from or approach and contact a platform CS are determined by the Pavlovian contingencies which render it a reliable signal for the occurrence or nonoccurrence of shock.     

Sign-tracking behavior in aversive conditioning: Its acquisition via a Pavlovian mechanism and its suppression by operant contingencies

When rats are presented with Pavlovian backward pairings in which shock is the unconditioned stimulus (US) and an elevated platform the conditioned stimulus (CS), they show a strong tendency to approach the platform. Attempts were made at evaluating the nature of the associative mechanisms responsible for the acwuisition and maintenance of the approach behavior. In Experiment 1, following a baseline period when platform presentations were given in the absence of shocks, first (training I), approach to the platform was prevented and subjects were exposed to either backward, forward, or random presentations of shock and platform: this procedure attempted to minimize the effects of response learning on the acquisition of approach behavior. Then (training II), all subjects received backward shock-platform pairings and had access to the platform. Approach to the platform was stronger in animals previously exposed to backward pairings than in the animals of the other two groups. Also, animals preexposed to forward platform-shock pairings showed suppression of approach behavior on the first trial of training II relative to their performance on the last trial of baseline. These data suggest that a stimulus-reinforcer learning mechanism alone is sufficent for the acquisition of approach. Experiments 2a and 2b evaluated the effects of “punishing” operant contingencies on Pavlovian-produced approach behavior. The results showed that approach can be eliminated, but only after repeated exposure to an operant contingency which consisted of the immediate closure of the platform upon approach responding. These data suggest that approach behavior produced by Pavlovian contingencies can be modified by operant contingencies. Taken together, these data provide additional support for a sign-tracking notion in aversive conditioning.     

The cognitive basis of the comprehension and production of relational terminology

The comprehension of big, little, and same number and the productio of relational terminology was assessed in 168 preschool children. Stimuli were used which varied the relationships of length, number, and density. Language comprehension and production were related to the complexity of cognitive operations required by the task. Specifically, comprehension was easier in the situations in which length and number were positively correlated than when length provided no cue to number. Comprehension was most difficult when length and number were negatively correlated. There was asymmetry in language comprehension such that the positive term big, was comprehended earlier than little in some tasks; there was also asymmetry in production in that the child was more likely to use language related to the positive pole than to the negative pole. These data were interpreted as providing support for theories of the cognitive basis of language acquisition.     

The effects of restraint and noncontingent preshock on subsequent escape learning in the rat

Three experiments investigated the effects of restraint and of inescapable fixed duration preshocks on subsequent shuttlebox escape-from-shock learning. Fixed-intensity preshock, random-intensity preshock, and no-preshock conditions were included in each experiment. In Experiment 1, restraining the rat in a harness prior to escape training retarded escape acquisition. There was no effect of preshock. In Experiment 2, both restraint and high fixed-intensity (1.0 mA) preshock retarded escape acquisition, when escape training occurred either immediately or 24 hr after preshock. In Experiment 3, movement was punished by positively correlating preshock intensity with the rat's movement; this treatment retarded escape conditioning. No effects were found for low fixed-intensity or random-intensity preshock nor for a condition in which movement was rewarded during preshock. The retarding effects of restraint and certain types of preshock were explained in terms of interfering instrumental responses.     

Spatial memory in rats under restricted viewing conditions

In a procedure devised by J. A. Walker and D. S. Olton (Learning and Motivation, 1979, 10, 73–84), rats were placed on two arms of a four-arm radial maze and then were placed in the center of the maze to test how accurately they could choose the alleys on which they had not been placed. In three experiments, the conditions under which animals viewed the environment from the arms were varied. In Experiment 1, both the extent of spatial view and the exposure time were varied factorially in a within-subjects design; animals viewed the environment down a tunnel or had a 180° or 360° view, and subjects were allowed to view the environment for either 2 or 20 sec. In Experiment 2, a between-subjects design was used, in which different groups of subjects were tested repeatedly under either the tunnel, 180°, or 360° conditions. Both experiments showed that animals could avoid the arms previously visited at no better than a chance level of accuracy in the tunnel viewing condition but could perform with progressively better accuracy at the 180 and 360° viewing conditions. Animals also were more accurate in Experiment 1 after viewing for 20 sec than after viewing for 2 sec. Experiment 3 involved a procedure in which restricted viewing conditions were used both during arm placements and testing. Animals tested under tunnel viewing eventually achieved above-chance performance with this procedure, but did not exceed chance as rapidly as groups tested with 45 and 90° views of the environment. These results suggest that animals can learn about their position in a spatial environment through observation and that an animal's ability to locate its position is directly related to the extent of the surrounding environment it can see and the length of time it is allowed to look. The implications of these findings for list and map hypotheses of spatial memory representation are discussed.     

Memory for lists of spatial events in the rat

Three experiments are reported in which rats were presented with lists of spatial events or responses in distinct visual contexts, and retention subsequently was measured for the events occuring at each serial position. In Experiments 1 and 2, lists contained different numbers of forced choices on successively presented T-mazes, and memory for each serial position was tested on each trial. In Experiment 3, lists were made up of different numbers of forced entries into randomly ordered arms on the eight-arm radial maze, and memory for one serial position was probed on each trial. All three experiments yielded serial position curves which demonstrated recency effects but no primacy effects. Comparisons of retention for different list lengths within each experiment indicated that retention of shorter lists was equivalent to retention of the final items of longer lists and superior to retention of the initial items on longer lists. This pattern of results indicated that there was no evidence of proactive inhibition in the serial position curves. Analysis of input and output interference effects and the results of control tests suggested that both retroactive inhibition and time-based forgetting processes were responsible for recency effects.