Binocular fixation in the newborn baby.

Three experiments are reported in which the newborn baby's ability to fixate binocularly was investigated, using the corneal reflection technique for measuring eye fixation position. Two criteria for consistent binocular fixation were assessed. These are (1) the two eyes will be optically more divergent when fixating more distant targets, and (2) each eye will be scored as being on-target when corrections for the expected deviations of the pupil center from the fixated stimulus are introduced.In the first experiment vertical arrays of lights were separately shown at distances of 10 and 20 in. from the subjects' eyes (with the retinal image size and luminance of the stimuli held constant). The 12 newborns who gave results at both viewing distances reliably converged to both stimuli, the optical divergence of the pupil centers of the eyes increasing with presentation of the more distant stimulus. In Expt 2 similar stimuli at 5 and 10 in. from the eyes were shown. It was again the case that the subjects reliably converged to the stimulus at 10 in. This was no so for the stimulus at 5 in., and many subjects fixated this stimulus with monocular vision. The failure to converge is probably due to an inability to accommodate to this near distance. In Expt 3 different stimuli (a vertical strip of light, an outline triangle and square, and an array of squares) were presented a constant distance (10 ± 1 in.) from the eyes. The majority of the 15 subjects binocularly fixated all three stimuli: for those subjects who failed to converge consistently to these stimuli the observed alternatives to binocular fixation were monocular fixation, divergent strabismus, and a third category of response that is most probably an indication of inattention to the stimulus. It can be concluded that the newborn baby possesses the ability to fixate binocularly an appropriately presented stimulus, and has the basic requirements for binocular vision.     

Functional significance of stimulus orientation: effects on orientation discrimination.

Children (6- and 9-year-olds) and adults were required to discriminate identical pairs of visual stimuli from mirror images. It was hypothesized that a key factor in performance would be the extent to which orientation was a functionally significant attribute of the stimuli. Two variables were manipulated, type of orientation discrimination and stimulus class. The first variable refers to the fact that the mirror images could be produced by either left/right or top/bottom reversals. Three classes of stimuli, varying in the extent to which a particular orientation was emphasized, were used: mobile objects (for which left/right orientation is assumed to be important); stationary objects (which lack comparable relevance for left/right orientation); and novel, abstract forms. The prediction was that if the discrimination task involved left/right reversals, as contrasted with top/bottom reversals, subjects would show an advantage for mobile objects, producing an interaction between stimulus class and orientation discrimination. In the first study, the subjects were children and performance was measured in terms of error rates. In the second study adults were tested, and reaction times were measured. Both studies manifested the predicted interaction. Results are discussed in terms of an information-processing framework, in which the incorporation of orientation-related features in the code representing a stimulus varies with the functional significance of the orientation to the stimulus class.     

The Random Stimulus Design

In the 1960s, a methodological advancement of significant proportion occured with the development of single case research designs in the field of appleid behavior analysis. Among the methods popularized were the multiple baseline, reversal, and, more recently, the alternating treatment designs. Despite the flexibility and wide applicability of each of these single subject designs, there are conditions under which none of them are appropriate. For example, when limited subjects are available and when repeated presentation of the same stimuli result in improvement due to practice effects of decremental effects due to boredom or habituation, problems arise. To offset this difficulty, the investigators describe a new single case design, the random stimulus design. This design is so named becuase an item pool of equal stimuli is established and then items are randomly selected and assigned to one of several cohorts. Cohorts are then assessed in the typical withdrawal or reversal manner.     

Stimulus selection with duration as a relevant cue

To date, research has not explicitly examined how duration competes with other stimulus dimensions for control over responding. The present study investigated some familiar selective mechanisms of stimulus control over key pecking in pigeons, with duration and line tilt as discriminative stimuli in successive discrimination procedures. Specifically, pigeon's key pecking was reinforced with food or extinguished following compound stimuli comprising one of two line orientation stimuli presented for one of two different durations. Traditional experimental designs explored stimulus additivity, overshadowing, blocking, and learned irrelevance. Although stimulus additivity was observed, control by duration was masked by line tilt in extinction testing that followed facilitated acquisition with redundant, relevant cues. In addition, although prior training with duration relevant partially blocked subsequent acquisition of control by line tilt when both stimulus dimensions were relevant, there was a tendency for control by duration to decrease with continued compound training. It was suggested that the greater time required to distinguish duration on a trial—compared to more commonly studied stimulus dimensions, which can be distinguished almost immediately—puts duration at a competitive disadvantage in situations where other relevant dimensions are also available.     

The logic of the stimulus

This paper examines the contribution of stimulus processing to animal logics. In the classic functionalist S-O-R view of learning (and cognition), stimuli provide the raw material to which the organism applies its cognitive processes–its logic, which may be taxon-specific. Stimuli may contribute to the logic of the organism's response, and may do so in taxon-specific ways. Firstly, any non-trivial stimulus has an internal organization that may constrain or bias the way that the organism addresses it; since stimuli can only be defined relative to the organism's perceptual apparatus, and this apparatus is taxon-specific, such constraints or biases will often be taxon-specific. Secondly, the representation of a stimulus that the perceptual system builds, and the analysis it makes of this representation, may provide a model for the synthesis and analysis done at a more cognitive level. Such a model is plausible for evolutionary reasons: perceptual analysis was probably perfected before cognitive analysis in the evolutionary history of the vertebrates. Like stimulus-driven analysis, such perceptually modelled cognition may be taxon-specific because of the taxon-specificity of the perceptual apparatus. However, it may also be the case that different taxa are able to free themselves from the stimulus logic, and therefore apply a more abstract logic, to different extents. This thesis is defended with reference to two examples of cases where animals' cognitive logic seems to be isomorphic with perceptual logic, specifically in the case of pigeons' attention to global and local information in visual stimuli, and dogs' failure to comprehend means-end relationships in string-pulling tasks.This contribution is part of the special issue “Animal Logics” (Watanabe and Huber 2006).     

Cognitive reference points

Two methods were used to test the hypothesis that natural categories (such as colors, line orientations, and numbers) have reference point stimuli (such as focal colors, vertical and horizontal lines, and numbers that are multiples of 10) in relation to which other stimuli of the category are judged. In Experiment I, subjects placed pairs of stimuli into sentence frames consisting of linguistic “hedges” such as “— is essentially—.” Results were that the supposed reference stimuli were most often placed in the second (reference) slot. In Experiment II, the subject placed a stimulus in physical space to represent his feeling of the psychological distance of that stimulus from another spatially fixed stimulus. Results showed that, when supposed reference stimuli were fixed, other stimuli were placed closer to them than vice versa. The results have substantive implications for the understanding of internal structure of categories and methodological implications for the mapping of reference points, quantification of linguistic intuitions, and the assumption of symmetry in psychological distance judgments.     

Pavlovian conditioning and rule learning

The experiment reviewed here was an attempt to show that two differential Pavlovian conditioning designs, namely positive and negative patterning, can best be understood as rule learning. First, it is shown that positive patterning is equivalent to the logical rule of conjunction (AND) and that negative patterning is equivalent to the logical rule of exclusive disjunction (XOR). It is assumed that in order to learn both kinds of discrimination subjects learn to use the according rule. If this is the case, the observed differentiation should be independent of the number of reinforcements for each individual stimulus. Second, subjects should be able to transfer the rule to new stimuli. Forty human subjects were randomly divided into four groups (N=10 each). Two factors were manipulated independently between subjects: (1) positive vs negative patterning, and (2) 2 vs 4 pairs of trained stimuli. Second interval skin conductance responses were measured. During initial acquisition positive as well as negative patterning occurred independently of number of pairs of trained stimuli (with total amount of training kept constant). Furthermore, AND as well as XOR could be transfered to new stimuli.     

Compounds of conditioned fear stimuli

A differential conditioning procedure was used with rats to establish different levels of suppression to two different stimuli. One stimulus was paired with shock every time it was presented, while the other stimulus cued shock on only 25% of its presentations. When these two component stimuli were subsequently tested as a simultaneous compound, two different types of component-compound relationships were observed. Some subjects showed greater suppression to the compound than they did to either component stimulus, while other subjects showed an intermediate level of suppression to the compound. The difference in type of component-compound relationship appeared to be related to the degree of stability (over trials) of each subject's reaction to the probabilistic (25%) cue.When a similar discrimination was established based on the intensity of the shock, rather than its probability of occurrence, all subjects showed more suppression to the compound than to its individual component stimuli. These results are discussed in terms of their implications for choice of model for characterizing the interaction of conditioned states.     

Paradoxical preference for more frequently occurring negative stimuli and for less frequently occurring positive stimuli as a function of amount of training in simultaneous discrimination learning

Development of a preference for more frequently occurring negative stimuli was found in a within-subject design. In this experiment, pigeons learned two simultaneous problems with an unequal number of training trials. At various stages in training, for example, the more-trained negative stimulus was paired with the less-trained negative stimulus for a single preference trial. These probe trials pointed to a swing in stimulus function in negative stimuli which also occurred at an earlier stage in positive (reward-correlated) stimuli. The paradoxical preference for less-trained positive over more-trained positive stimuli was found in this study, confirming the earlier reported phenomenon. The paradoxical preference for more-trained negative stimuli was discussed in terms of a frustration analysis. A symmetrical, albeit positive, emotional factor was discussed with regard to the paradoxical findings with positive probe trials.     

Foreperiod and visual stimulus intensity: A reappraisal

The joint effects of stimulus modality, stimulus intensity, and foreperiod on simple RT were investigated. In experiment 1 an interaction was found between stimulus intensity, both visual and auditory, and a variable FP such that the intensity-effect on RT was largest at the shortest FP. Experiment 2 provided a successful replication with smaller and weaker visual stimuli. No interaction was observed with a constant FP, although the visual stimuli were identical and the auditory ones psychophysically equivalent to the visual stimuli of experiment 1.It is proposed that an additive or interactive relationship between stimulus intensity and FP can be inferred only when the mental processes called for by the various uses of FP are simultaneously considered. Another precondition is an adequate sampling of the intensity-continuum with special reference to the retinal size of visual stimuli.     

Hemispheric asymmetries in human infants: Spectral analysis of flash and click evoked potentials

Evoked potentials of 16 human infants (mean age = 5.0 weeks, SD = 1.8 weeks) were recorded from the left and right, occipital and temporal areas. Spectral analysis showed a high amplitude, localized, coherent center of activity within the left temporal area for click stimuli, and a high amplitude, localized center of activity in the right occipital area for flash stimuli. It was proposed that the structured auditory information of the click and the unstructured visual information of the flash represented different degrees of familiarity to the subjects. With this hypothesis, left hemisphere involvement in stimulus processing would increase as the stimulus became more referrable to previous long- or short-term experience. Conversely, right hemisphere involvement would increase with unfamiliar stimuli which could not be readily associated with earlier data.     

Wyckoff's observing response: Pigeons learn to observe stimuli for free food but not stimuli for extinction

Four pigeons received periods of free food delivery alternating with periods of extinction. The experimental chamber was divided in half. Initially the subjects could produce stimuli selectively associated with these schedules by standing on the right side of the chamber and later by standing on the left side. In both phases, subjects produced the free food stimulus most of the time it was available but did not increase above baseline the time spent producing the extinction stimulus. Thus, when alternative stimuli are available, the pigeon prefers the stimulus associated with the greater frequency of reinforcement although the choice results in no biological advantage.     

Transfer of conditioned appetitive stimuli to conditioned aversive excitatory and inhibitory stimuli

The transfer of Pavlovian appetitive stimuli to Pavlovian aversive stimuli was examined in three experiments. In Experiment 1, rats received appetitive (Ap) conditioning designed to establish a flashing-light stimulus as either a CS+, CSo, or CS? for food, or to maintain it as a novel stimulus for US-alone subjects. Then, the stimulus was employed as a signal for weak shock in conditioned-emotional-response (CER) training. Both acquisition and extinction results showed that the ApCS+ facilitated and the ApCS? retarded aversive excitatory conditioning relative to the ApCSo and US-alone controls. Experiment 2 replicated the findings of Experiment 1 with both a moderate and a severe shock in CER training. In Experiment 3, different groups received the same appetitive conditioning as before, but to a flashing-light stimulus which was then employed as a signal for no shock in CER training. The ApCS? facilitated and the ApCS+ retarded aversive inhibitory conditioning relative to ApCSo and US-alone controls. Collectively, these findings establish that, in Pavlovian conditioning, transfer of an appetitive CS to an aversive excitor or inhibitor is facilitated by maintaining the initial conditioning contingency.     

Stigma,staring, and discomfort: A novel-stimulus hypothesis

Three experiments were conducted in order to assess the validity of the novel-stimulus hypothesis as an explanation for why people who are physically different (i.e., novel) are avoided. The hypothesis states that avoidance is mediated by conflict over a desire to stare at novel stimuli and a desire to adhere to a norm against staring when the novel stimulus is another person. In the first two field experiments, subjects viewed photographs of novel (handicapped or pregnant) and familiar (physically normal) people under conditions where staring was sanctioned or not. It was found that staring increased with novelty when staring was unobserved (sanctioned); however, the reverse obtained when an observer was present. In the third experiment, subjects interacted with a crippled, pregnant, or physically normal partner. Half of the subjects were first given the opportunity to observe their partner through a one-way mirror. The reduction in stimulus novelty for this group resulted in reduced avoidance. The question of whether such avoidance of the disabled results from feelings of dislike or disgust as previously suggested, or from discomfort created by novelty, is discussed.     

Exposure effects and associative learning

The contributions of initial stimulus affect and of associative learning to the effects of repeated stimulus exposures were examined in two experiments. Stimuli that were initially positive and stimuli that were initially negative were presented for different number of times, and subjects rated these stimuli afterward on a number of affective dimensions. In all cases, except when negative affect was associatively paired with every stimulus exposure, affective responses became increasingly more positive with increasing exposures. The results were taken to indicate that the exposure effect can overcome an initially negative stimulus affect when the conditions of the mere exposure hypothesis are satisfied. Initial stimulus affect and associative learning of affect were shown to be independent factors, the first influencing the intercept of the exposure function, the second its slope.     

女性对新异性事件加工的偏向:来自ERP的证据

采用修订后的oddball范式,结合ERP技术考察女性与男性在加工中性新异刺激时的差异。ERP结果表明,在早期已经出现新异性效应。在300-500ms内,新异刺激在男性和女性被试中都比标准刺激诱发了更大的LPC。在500-700ms内,新异刺激仅在女性被试中比标准刺激诱发更大的LPC,在男性被试中没有显著差异。这些结果表明男性和女性都对中性新异刺激表现出加工偏向,但是女性对其加工的时间比男性更长。这可能与女性容易对显著性(salient)的刺激进行沉思(rumination)相关。     

Second-order conditioning with diffuse auditory reinforcers in the pigeon

Pigeon subjects were used in five experiments investigating second-order conditioning with visual second-order and diffuse auditory first-order stimuli. Experiment 1 used a discriminative conditioning procedure to demonstrate reliable and substantial second-order conditioning with these stimuli. In Experiments 2 and 3, extinction of the auditory first-order stimulus after second-order conditioning had little effect upon responding to the second-order stimulus, when compared to a stimulus whose reinforcer was maintained. Experiment 4 compared directly the susceptibility of second-order responding to extinction of the first-order reinforcing stimulus as a function of the modality of that reinforcer. When a visual second-order stimulus was paired with a visual reinforcer, and the response to the latter was extinguished, then second-order responding was greatly reduced relative to control levels. In contrast, when that reinforcer was an auditory stimulus, second-order responding was not affected by the current value of the first-order stimulus after conditioning. Finally, in Experiment 5 the auditory stimulus was established as a reinforcer through discriminative-operant training. Following second-order conditioning, extinction of responding to this stimulus again had little impact upon responding to the second-order stimulus with which it had been paired. These results are discussed in terms of previous work on second-order conditioning with rat and pigeon subjects.     

An analysis of generative representation systems

Three ideas are basic to generative theory: (a) Subjects are assumed to attend to the relations among stimuli, extracting the transformations relating pairs of stimuli; (b) the set of abstracted transformations is decomposed or reduced to an elementary set of generators; (c) subjects use the elementary generators as the basis for judging similarity. The purpose of this paper is to illustrate these ideas with an experiment in which subjects were asked to rate the similarity between stimulus pairs. The stimulus materials consisted of the permutations of a 4-item pattern with the properties of a dihedral group which insured the existence of sets of elementary transformations. Three analytic techniques were used to determine the generator set of transformations abstracted by subjects. The first analysis consisted of a monotonic regression between dissimilarity ratings and the number of elementary generators of a given permutation. The residual variance of this monotone regression, suitably normalized, was used as a quantitative goodness-of-fit measure. For the stochastic analysis, cumulative distributions of dissimilarity ratings were obtained for permutations requiring one, two, or three generators. The idea was that permutations requiring fewer generators should be associated with distributions of lower dissimilarity values (higher similarity scores) as compared to permutations predicted to be transformationally more complex. The final analysis, a multidimensional scaling of dissimilarity ratings, converted subjects' ratings into spatial structures to determine whether individual subjects' ratings exhibited the predicted spatial arrangement. The monotone regression and stochastic analyses abstracted similar generator sets for individual subjects, some of which provided perfect fits to the data. Although the scaling analysis yielded similar estimates of generators, for some subjects, transformations with the same number of generators yielded unequal “cognitive” distances resulting in some-what deformed spatial structures for these subjects. It was concluded that the results generally supported a generative model as an approximation to subjects' representations of interstimulus relationships.     

Information integration in price-quality tradeoffs: The effect of missing information

Support for averaging processes in information integration has relied on experimental designs in which the amount of information to be integrated was varied. The usual interpretation is that subjects balance the values of the various stimuli presented on a given trial. An alternative interpretation is that subjects may use their perceptions of the relationship between stimulus dimensions to infer the value of missing information. In the present study, subjects were asked to rate their expected satisfaction with purchases of ground beef on the basis of quality and/or price information. The responses of some subjects appeared to be based on the inference that high prices imply high quality and low prices imply low quality when no quality information is given. Other subjects appeared to assign a constant value to missing information. An averaging model that incorporates inferred as well as presented stimulus values is proposed.     

Interaction Between Visually and Kinesthetically Triggered Voluntary Responses

A voluntary motor response that is prepared in advance of a stimulus may be triggered by any sensory input. This study investigated the combination of visual and kinesthetic inputs in triggering voluntary torque responses. When a visual stimulus was presented alone, subjects produced a fast and accurate increase in elbow flexion torque. When a kinesthetic stimulus was presented instead of the visual stimulus, subjects produced a similar response with a reduced response latency. When a visual stimulus was presented in combination with a kinesthetic stimulus, subjects initiated their responses after either a visual or a kinesthetic response latency, depending on the relative timing of the two stimuli. An analysis of response amplitude suggested that when visual and kinesthetic stimuli were combined, both stimuli triggered a response. The results are more consistent with a simple behavioral model of addition of visual and kinesthetic responses (which predicts that the response to combined stimuli should be the sum of individual responses) than with a model of exclusion of one response (which predicts that the response to combined stimuli should be identical to either the visual or the kinesthetic response). Because addition of visually and kinesthetically triggered responses produced a response with an erroneously large amplitude, it is suggested that visual and kinesthetic inputs are not always efficiently integrated.