Generalization of visual matching and delayed matching by a California sea lion (Zalophus californianus)

Only a limited number of species have been found capable of generalized matching-to-sample (MTS) after exposure to relatively few training exemplars. We trained a juvenile, experimentally naive California sea lion (Zalophus californianus) in MTS, using a pair of three-dimensional objects as samples. Successful matching to a criterion of 90% correct or better over 2 successive sessions was attained in 12 sessions (269 trials and 70 errors). Two subsequent “partial” transfer tests, in which each of the two training objects was paired with a novel test object, and four additional transfer tests, all with novel objects, were presented following training. An 80% performance criterion over 2 successive sessions was reached, or closely approximated, in from 2 to 4 transfer sessions for all transfer tests; errors to criterion tended to be reduced across the successive novel transfer tests and were as few as five during the final two tests; and performance on the first 48 trials of the last two novel transfers was not significantly different from a near-ceiling level baseline performance measure. Neophobic responses of the sea lion to new objects precluded an unbiased evaluation of immediate (Trial 1) transfer. The sea lion’s short-term memory for sample objects was also measured. Matching performance was maintained at a level of 78% correct responses or better for delays through to 45 sec after removal of the sample object. At a 58-sec delay, the longest tested, performance declined to 69% correct responses. These retention levels are only somewhat below levels reported for dolphins and nonhuman primates tested on visual delayed MTS, but they are above levels typically reported for pigeon subjects.     

Auditory matching-to-sample in monkeys (Cebus apella)

Four of 8 monkeys were successfully trained on an identity matching-to-sample task employing two acoustic stimuli. In five subsequent tests with different pairs of auditory stimuli, their performances were at levels that provided strong evidence for concept-mediated transfer. Thus, despite past failures to demonstrate the matching concept in the auditory modality, the present results indicate that the matching concept is not limited in monkeys to the visual modality. On the other hand, the failure of 4 subjects to learn the initial matching task constitutes additional evidence of cognitive asymmetry in monkeys with regard to the visual and auditory modalities.     

Oddity of visual patterns conceptualized by pigeons

Pigeons were trained to learn an instrumental oddity-from-sample discrimination involving visual forms. One group, the “few examples” group, dealt with 5 patterns in 40 different combinations. Another group, the “many examples” group, dealt with 20 patterns in 160 different combinations. After both groups had reached asymptotic performance and had learned to operate under partial reinforcement conditions, they were tested for transfer under extinction conditions with two different groups of 5 novel patterns, each in 40 combinations. All animals showed significant above chance transfer to both of these novel stimulus sets. Transfer performance with test stimuli of similar geometric design to training stimuli was better than performance with stimuli of markedly different design. The transfer performance of the “many examples” group was marginally better than that of the “few examples” group, even though the latter’s performance on the training stimuli was better throughout. It is concluded that pigeons can learn to employ an oddity concept and that this may be promoted by the use of many training exemplars. Furthermore, it is inferred that pigeons may normally use a mixture of strategies to solve oddity and identity problems.     

Some tests of the anticipatory mediated generalization model of acquired sample equivalence in pigeons’ many-to-one matching

Transfer-of-control tests typically show the development of acquired equivalence between samples occasioning the same comparison choice in pigeons’ many-to-one matching-to-sample. Specifically, when some of those samples are later explicitly trained to occasion new comparison choices, the remaining samples immediately exert control over the new choices as well. In the present experiments, we examined whether or not this transfer effect depends on the order in which the various sample-comparison relations in training are learned. One group of pigeons initially acquired 0-delay many-to-one matching with four samples and two comparisons, followed by 0-delay matching with two of those samples and two new comparisons. Another group of pigeons learned the two-sample matching task first, followed by many-to-one matching. When subsequently tested for their ability to match the remaining samples from many-to-one matching to the comparisons used in the two-sample task, both groups showed comparable levels of transfer. These findings challenge the view that common anticipatory processes ostensibly arising from the samples in many-to-one matching are necessary mediators for the subsequent transfer effects indicative of acquired sample equivalence.     

An analysis of visual oddity concept learning in a California sea lion (Zalophus californianus)

We tested a California sea lion for visual oddity learning by presenting problems composed of three two-dimensional black-and-white stimuli, two identical (S−) and one different (S+). In the first experimental stage, a single problem per session was presented until learning criterion was reached. In the second experimental stage, all problems were presented only five times in succession; then a new problem was introduced (six problems/session). In the third experimental stage, each problem was presented only once. The sea lion mastered all stages of oddity learning. A final transfer test with oddity problems composed of completely new stimuli yielded performance significantly above chance. Data analyses suggested learning of specific stimulus properties in the first stage, learning set formation in the second stage, but oddity conceptualization in the third stage.     

Concept learning by pigeons: Matching-to-sample with trial-unique video picture stimuli

Pigeons were trained to match-to-sample with several new methodologies: a large number of stimuli, computer-drawn color picture stimuli, responses monitored by a computer touch screen, stimuli presented horizontally from the floor, and grain reinforcement delivered onto the picture stimuli. Following acquisition, matching-to-sample concept learning was assessed by transfer to novel stimuli on the first exposure to pairs of novel stimuli. One group (trial-unique), trained with 152 different pictures presented once daily, showed excellent transfer (80% correct). Transfer and baseline performances were equivalent, indicating that the matching-to-sample concept had been learned. A second group (2-stimulus), trained with only two different pictures, showed no evidence of transfer. These results are discussed in terms of the effect of numbers of exemplars on previous failures to find concept learning in pigeons, and the implications of the positive finding from this experiment on abstract concept learning and evolutionary cognitive development.     

Cross-stimulus transfer of timing in pigeons

Pigeons were trained in a delayed matching task in which the samples were short (2 sec) and long (10 sec) presentations of either a houselight or a keylight. Transfer trials involved short and long presentations of the nontrained signal as the sample. In the intermittent transfer test, infrequent transfer trials were intermixed with more frequent training trials; in the sustained transfer test, all trials were transfer trials. The intermittent test revealed only weak transfer. The sustained test revealed transfer in Session 1 only in birds that had received pairings of the transfer signal and food prior to testing. However, regardless of whether the transfer signal had been previously paired with food, birds exposed to consistent contingencies between duration and choice across training and testing learned the transfer task more rapidly than did birds exposed to inconsistent contingencies. It was concluded that some training in which the transfer signal serves as the sample is required before the durations of a transfer signal are related to the rules associating duration and responding     

The search for symmetry: 25 years in review

It has been 25 years since the publication of Sidman et al.’s (1982) report on the search for symmetry in nonhuman animals. They attributed their nonhuman subjects’ failure to the absence of some critical experiences (e.g., exemplar training, control of location variables, and generalized identity matching). Since then, species ranging from rats to chimpanzees have been tested on symmetry, and the results have been equivocal. Twenty-four investigations of symmetry in nonhumans are reviewed to determine whether the underlying factors first addressed by Sidman et al. (1982) have been verified and whether new factors have been identified. The emergent picture shows that the standard procedures as typically implemented on a three-key apparatus are insufficient by themselves to produce emergent symmetry in nonhumans. Recent successful demonstrations of symmetry in sea lions and pigeons have clarified certain important stimulus control variables (i.e., select and reject control) and suggest avenues for future research. Reliable symmetry may be achievable with nonhumans if training and test procedures that encourage compatible stimulus-control topographies and relations are designed.     

Differential effects of omitting comparison stimuli on symbolic and identity matching to sample: Evidence for altered instructional processes in pigeon short-term memory

Two experiments were performed to determine the effects of omitting the comparison stimuli in a matching-to-sample task. In Experiment 1, birds were trained initially on both symbolic and identity matching to sample. Comparison stimuli were then omitted following the presentation of a particular sample stimulus, and this decreased the number of sample (observing) responses. The reintroduction of the comparison stimuli on subsequent probe trials revealed that the accuracy of symbolic matching was reduced to chance levels, while identity matching accuracy was significantly below chance. In Experiment 2, a similar procedure was employed; however, observing responses to the comparison-omitted samples were maintained by direct reinforcement (fixed ratio 20). Matching accuracy during probe trials was again at chance levels for symbolic matching but, contrary to Experiment 1, was significantly above chance for identity matching. The differential effects of omitting comparison stimuli on symbolic and identity matching trials in these two experiments were interpreted within a framework which assumes that instructional processes are altered by comparison-omission procedures.     

Effects of process-oriented worked examples on troubleshooting transfer performance

In the domain of electrical circuits troubleshooting, a full factorial experiment investigated the hypotheses that (a) studying worked examples would lead to better transfer performance than solving conventional problems, with less investment of time and mental effort during training and test, and (b) adding process information to worked examples would increase investment of effort during training and enhance transfer performance; whereas adding it to conventional problems would increase investment of effort, but would not positively affect transfer performance. The first hypothesis was largely confirmed by the data; the second was not: adding process information indeed resulted in increased investment of effort during training, but not in higher transfer performance in combination with worked examples.     

Effects of sample duration,retention interval,and passage of time in the test on pigeons’ matching-to-sample performance

Four pigeons served as subjects in an experiment using the go/no-go delayed matching-to-sample paradigm. The go/no-go method was used because it permits the experimenter to track the time course of discriminative performance throughout the test period, unlike the conventional choice matching procedure. It was found that discriminative test performance increased with longer sample durations; performance decreased with longer retention intervals and also as time passed in the test period. The rate of forgetting was virtually the same when either the retention interval was lengthened or time elapsed in the test. These findings support a modified trace theory, which proposes that the sample stimulus trace decays at a constant rate from the point of sample offset, and that the decaying memory trace is repeatedly compared with the prevailing test stimulus as time passes in the test period.     

Symbolic,identity, and probe delayed matching of sounds by the bottlenosed dolphin

The short-term memory for sounds of the bottlenosed dolphin was tested using symbolic, identity, and probe forms of the delayed matching-to-sample (DMS) task. The forms differed in the number (one or two) or nature (symbolic or identity matches of sample sounds) of postdelay test stimuli available as memory retrieval cues. Although symbolic DMS was difficult to learn, the final performance level was approximately equal to that for identity or probe DMS. On all tasks, the dolphin’s responses were above 80% correct through to delays of 90 sec and, in some cases, through to delays of 180 and 240 sec, the “limits” being governed mainly by the dolphin’s reluctance to continue being tested at long delays. Encoding of sample stimuli into their learned symbolic representation was hypothesized to have reduced symbolic DMS to a recognition memory task, resulting in the observed equivalence of performance with the other two recognition memory tasks. The probe DMS results, unlike those for identity or symbolic DMS, showed no significant proactive interference effects from samples of prior trials. Instead, proactive interference was traceable to the probe value of the prior trial. Overall, the auditory DMS data for the dolphin were functionally similar to results reported for monkeys tested on symbolic, identity, and probe visual DMS tasks.     

Development of excitatory backward associations during the establishment of forward associations in a delayed conditional discrimination by pigeons

The development of excitatory backward associations in pigeons was demonstrated in three experiments involving conditional discriminations with differential outcomes. In Phase 1 of all three experiments, correct comparison choices following one sample were followed by food, whereas correct comparison choices following the other sample were followed by presentation of an empty feeder. In Phase 2, the food and no-food events that served as outcomes in Phase 1 replaced the samples. When the associations tested in Phase 2 were consistent with the comparison-outcome associations developed in Phase 1, transfer performance was significantly better than when the Phase 2 associations were inconsistent with the Phase 1 associations. In Experiment 1, an identity matching-to-sample task was used with red and green samples and red and green comparisons. In Experiment 2, a symbolic matching task was used with shape samples and hue comparisons, and it was shown that the backward associations formed were between the trial outcome (food or no food) and the correct comparison. In Experiment 3, it was determined that the transfer effects observed in these experiments did not depend on either the similarity of behavior directed toward the samples in the training and test phases, or the similarity of food and no-foodexpectancies generated by the samples in Phase 1 to food and no-foodevents presented as samples in Phase 2.     

Control of delayed matching-to-sample performance using directed forgetting techniques

Pigeons acquired a successive delayed matching-to-sample task at a delay interval of 4 sec. Instructional stimuli were interpolated in the delay interval signaling the occurrence (R-cue) or nonoccurrence (F-cue) of comparison stimuli, a procedure modeled after the directed forgetting techniques commonly used in human memory studies. Accuracy on probe trials (in which comparison stimuli were presented following F-cues) was reduced relative to performance on standard training trials in which R-cues signaling the occurrence of comparison stimuli appeared in the same temporal location. The extent of the reduction in accuracy depended on the temporal location of the F-cues, the reduction being greater when the cue was more remote from the comparison stimuli. Examination of retention interval keypecking revealed a strong correlation between matching performance and retention interval responding.     

Cumulative proactive interference in animal memory

Events occurring on the prior trial in delayed matching-to-sample tasks can proactively interfere with accurate matching on the current trial. The present study investigated the accumulation of proactive interference in delayed matching-to-sample at the local level of two consecutive trials, as well as in terms of a general performance decrement accumulating over the session. Higher-order analyses, in terms of the parameters of negative exponential functions fitted to the data, showed that the magnitude of the local proactive-interference effect resulting from inter-trial disagreement of stimuli decreased over the session. Furthermore, there was no evidence for the general performance decrement over the session, which is frequently attributed to proactive interference. The attenuation of the local proactive-interference effect was accounted for in terms of changes in the relative probabilities of agreeing and nonagreeing trials.     

Preliminary evidence for color stimuli discrimination in the Asian small-clawed otter (Aonyx cinerea)

Color discrimination ability can be determined through anatomy or perceptual ability. In this study we tested perceptual ability. Three Asian small-clawed otters (Aonyx cinerea), one male and two females, were trained via operant conditioning to discriminate stimuli within a training task. If they passed criteria for this task, they were tested on as many as six delayed matching-to-sample experimental tasks. These experimental tasks involved comparing varying saturations of the colors blue, green, and red against varying shades of gray, as well as against each other. The male reached criterion on five of the experimental tasks, indicating an ability to discriminate the stimuli. One female participated in only two tasks and did not achieve the criteria as set. The second female did not pass the training task, and thus was not experimentally tested. This study overall showed some early evidence that Asian small-clawed otters may have the ability to learn to discriminate different stimuli on the basis of color cues. Sensory studies conducted on two other otter species and the results of this study indicate that color vision may be a common trait across Lutrinae species.     

Directed forgetting effects in pigeons: Remember cues initiate rehearsal

Pigeons were trained in a two-choice delayed matching-to-sample task with red and green hues. A brief postsample cue (a vertical or horizontal line) signaled whether the comparison stimuli would be presented or omitted on each trial. Comparison stimuli were always presented following the remember-cue (R-cue) trial, but never following the forget-cue (F-cue) and no-cue trials. In Experiment 1, matching accuracy on F-cue and no-cue trials was equivalent and was considerably inferior to accuracy on R-cue trials. In Experiment 2, the placement of the postsample cue was manipulated. Matching accuracy decreased as the R cue was delayed in the retention interval, but performance in the F-cue condition was not affected. These data indicate that the no-cue condition can function as an implicit F cue and that the R cue can function to initiate and maintain rehearsal.     

Training Transfer and Transfer Motivation: The Influence of Individual,Environmental, Situational,Training Design,and Affective Reaction Factors

The purpose of this study is to examine the effects of individual, environmental, training design, and affective reaction factors on training transfer and transfer motivation. To determine the relationship between these factors and their influence on training transfer and to test the model, the researchers collected data from employees in the Malaysian banking sector. Structural equation modeling with Amos 16 was used to test the model and determine the relationship. The study suggested that training stakeholders should manage the training program effectively. Transfer is maximized when trainees have social support, high performance self‐efficacy, and transfer motivation. Stakeholders (e.g., trainers, trainees, supervisors, and peers) are important to the training transfer process, as are learner readiness, trainee reaction, instrumentality, and training retention. This study revealed that perceived content validity and transfer design work together and influence the trainee's performance self‐efficacy. In other words, if trainers want to improve the performance self‐efficacy level of trainees, they need to explain how the trainee can transfer the learned skills at the workplace and make sure the content of the training is similar to the actual job. The main objective of training programs is to align the employee's expertise with organizational goals. Organizations can achieve their desired objectives only when employees transfer the learned skills on the job. Unfortunately, employees often transfer only a small percentage of skills they have learned in training. To effectively manage their training programs, organizations need to identify and focus on the factors that resist effective training transfer.     

Associatively activated representations of food events resemble food outcome expectancies more closely than they resemble food-based memories

When Pavlovian stimuli activate representations of food, do these representations resemble memories of food consumed in the recent past or expectancies of food that is imminent? In Experiments 1A and 1B, this question was addressed by training pigeons on a symbolic matching-to-sample task involving different grains as memory cues or as expectancy cues for correct choices. Autoshaping trials involving these same grains were interspersed among matching-to-sample trials, as were test trials involving the substitution of autoshaping stimuli for cues in the matching-to-sample task. Control over choices transferred to autoshaping stimuli in both experiments, suggesting that associatively activated representations of food resemble both memories and expectancies. In Experiment 2, pigeons were trained on a symbolic matching-to-sample task in which food and no-food memory cues (i.e., the samples) were juxtaposed with no-food and food expectancy cues. Subsequently, autoshaping stimuli, which activated representations of food and no food, were substituted for the samples. Choices by the pigeons indicated that associatively activated representations of food-related events resemble expectancies more closely than they do memories.     

Contextual stimuli and memory retrieval in pigeons

Pigeons were given free-operant successive discrimination training in which, on alternate days, two different interdimensional problems were employed (color positive and line angle negative; a different color negative and a different line angle positive). Between days, these problems could be construed as intradimensional ones. For one group, training was conducted on each problem in the presence of the same ambient (contextual) stimuli, while for a second group each problem was trained in a different context. For a third group, these two contexts were randomly related to the problems. Postdiscrimination stimulus generalization gradients showed that peak shifts were obtained in both the same context and the random context groups, but no peak shifts were found for the group which learned each problem in a different context. Results were consistent with Spear’s (1973) treatment of animal memory which attributes retention test performance to the operation of a “context-elicited” retrieval process. An alternative uniprocess conditioning account of these and similar data was also discussed.