Individual differences in the verbal coding of familiar visual stimuli

Two experiments were performed both of which involved the same-different comparison of pairs of alphabet letters. "Same" reaction times were obtained for both physical matches (e.g., AA) and name matches (e.g., aA). The results of both experiments supported the hypothesis that individual subjects would differ with respect to whether or not they based their physical matches on a comparison of verbal codes. In Experiment I, subjects differed in the size of their reaction time difference between physical and name matches, and in Experiment II, individuals differed with respect to whether or not the frequency of usage of the letters affected their reaction time for physical matches. In both experiments, the individual differences in verbally coding physical matches were related to Hock's (1973) individual differences distinction between subjects emphasizing analytic processes and subjects emphasizing structural processes.     

Laterality effects in visual information processing: Hemispheric specialisation or the orienting of attention?

The notion that visual laterality patterns may be attributable to attentional allocation rather than hemispheric specialisation was examined in three experiments. In Experiment I, high verbal ability subjects were found to be less lateralised on a letter name match task than low verbals. In Experiment II, stimulus probability was shown to affect laterality patterns for name but not for physical matches. Again, low verbals were affected more than highs. Experiment III produced results identical to those of Experiment II although, in the latter experiment, visual fields were defined vertically rather than horizontally from the midline. Together, these results support the following generalisations: (1) visual asymmetries have their locus in a post-perceptual information processing stage; (2) visual asymmetries may be altered by manipulating stimulus probability; (3) verbal ability differences in laterality may not reflect neuroanatomical differences but merely cognitive capacity and (4) it may be unnecessary to invoke differential hemispheric specialisation in order to account for visual lateral asymmetries.     

Switching attention within and between categories: Evidence for intracategory inhibition

In a variation of the Posner and Snyder (1975b) paradigm, subjects made speeded “same” or “different” responses to pairs of digits or letters on the basis of name identity (Experiment 1) or physical identity (Experiment 2). Each target pair was preceded by an informative (letter or digit) or noninformative (plus-sign) warning signal. The letter or digit represented by an informative warning signal had a high probability of appearing in the subsequent target pair (expected condition). On trials in which the expected stimulus did not appear in the target pair, the target pair belonged with equal probability to either the same category (either letters or digits) as the expected stimulus or to the opposite category (unexpected-similar and unexpected-opposite conditions, respectively). The pattern of “benefits” and “costs” of attentional expectancy found by Posner and Snyder for “same” responses was replicated: Subjects were faster and more accurate in the expected condition than in the neutral (uninformative warning signal) condition, but slower and less accurate in the unexpected conditions. Present theoretical interest concerns “same” response times and accuracy for the two unexpected conditions. Under instructions emphasizing accuracy as well as speed (Experiments 1 and 2), performance was worse in the unexpected-similar condition than in the unexpected-opposite condition. Only when instructions deemphasized accuracy (Experiment 2) was performance better in the unexpected-similar condition than in the unexpected-opposite condition. The fact that subjects may have more difficulty switching attention within a category than between categories (at least when instructions emphasize accuracy as well as speed) contrasts sharply with current theoretical emphasis on intracategorical facilitation effects in the priming paradigm. The results are interpreted within the framework of a model of attention (Keele & Neill, 1978) in which the activation of associates to the focus of attention is actively and optionally suppressed so as to reduce present or potential interference with the focal information processing.     

Temporal aspects of selective masking

In two experiments, rows of random letter sequences were presented for 100 ms and were patterned masked at varying delays after display offset. In Experiment I recall was probed by visual partial report cues, while auditory probes were employed in Experiment II. Compared to no-masking control conditions, the masking stimulus had a selective effect at the different positions of the rows. The masking stimulus produced the largest decrements in recall of letters from the centre positions of the displays but had a minimal effect on performance at either end of the rows. Furthermore, it was demonstrated that improvements in recall were limited to the centre positions of the rows at increased delays of mask. Subsidiary analyses revealed that processing of the end letters of the displays terminates shortly after display offset while processing of the centre letters continues for at least 500 ms. The results are consistent with the notion that processing of multi-letter arrays commences at the ends of the rows and that the selective masking effect reflects the order of processing of the contents of iconic memory. However, these results were evident only in Experiment II which employed auditory partial report cues. When the partial report cues were visual, there were no effects of masking and minimal increases in performance at increased delays of mask. The discrepant results of the two experiments are discussed in terms of process interruption caused by obligatory attention to the partial report cues.     

Encoding processes in memory scanning tasks

Three experiments are presented that deal with the effect of stimulus probability on the encoding of both alphanumeric characters and nonsense figures. Experiment I replicated a previous finding of an interaction between stimulus probability and stimulus quality in a memory scanning task with numbers as stimuli. Experiments II and III investigated the same paradigm with unfamiliar visual forms as stimuli, and no interaction was found. Results were interpreted as showing that probability affects the encoding mechanism only when the encoding process results in a representation of the name of the stimulus. When stimulus materials are visual forms without names, probability does not appear to affect encoding processes.     

Interactions among levels of processing

This article examines associations among representations of physical, name, and category information by determining effects of category repetition on and following physical, name, and category match trials. Subjects decided whether two letters were from the same half of the alphabet. Category repetition effects were evidenced by faster ~nd more accurate responses when letters from the same half of the alphabet were used on successive trials. Although physical matches showed no effect of category repetition, name and category matches did. Trials following physical matches were less affected by category repetition than were trials following name or category matches. The results suggested that these category repetition effects were mediated by interletter associations: Reaction time increased with the alphabetic distance between preceding and current letters. However, these distance effects held only for forward (A → B) and not backward (B → A) alphabetic sequences, suggesting that the alphabetic representation is ordinal and unidirectional.     

无意识信息的刺激表征及其时间特性

无意识信息是否存在刺激表征有待解决。实验采用字母Flanker任务, 通过目标和flanker在刺激水平和反应水平上的冲突效应, 重点考察阈下flanker在刺激水平的表征。在相同的实验设计下, flanker可觉察时(实验1A), 观察到经典的刺激冲突效应和反应冲突效应; 而flanker无意识时(实验1B), 重复了反应冲突效应, 却观察到刺激冲突效应发生反转, 提示了无意识信息的反应加工及刺激加工。实验2采用符号材料促使刺激−反应的自动联结, 减少刺激−反应规则的难度, 结果重复了实验1B的发现--无意识信息引起反转的刺激冲突。刺激冲突下反转效应的一致结果表明无意识信息的刺激表征影响了认知加工。实验3考察这种影响在时间进程上的特点。无意识刺激表征的影响随反应时变化：在快速反应中观察到刺激冲突效应, 之后该效应发生反转且反转量随反应时增加而增大。相反, 无意识反应表征的影响在不同反应时下保持稳定。以上结果提供了无意识信息存在刺激表征的行为学证据并揭示了其时间特性, 提供了无意识领域中不一致研究结果的整合思路。     

Using visual codes for comparisons of pictures

In two experiments, Ss indicated for a series of trials whether or not two pictures of common objects had the same name (a positive or negative response, respectively). The pictures were separated by one of three interstimulus intervals (ISis), and reaction time (RT) was recorded. In Experiment I, positive trials involved pictures that were identical (identity match), mirror images (mirror match), or physically different but had the same name (name match). The stimuli came from either an S set, in which name-match pairs were physically similar, or a D set, in which name-match pairs were physically dissimilar. The mean RTs for mirror and identity matches were virtually the same but faster than name-match RTs, an advantage that decreased with increasing ISI. It was expected that name-match RT for the S set would be less than for the D set, indicating a facilitative effect of physical similarity; however, the identity-match RTs showed the expected difference. These results were extended in Experiment II, which involved only the identity and name matches, in pure sessions (which included positive trials of just one type) or mixed sessions (which included both types of positive trials). For mixed sessions, name- as well as identity-match RTs differed between the S and D sets. These results provide evidence for the use of visual codes in comparing nonidentical pictures, codes that apparently vary with experimental context and task demands.     

Levels of processing in disruptive effects of prior information

Under certain conditions, advance information about possible letter alternatives may depress recognition of single tachistoscopically presented letters followed by a pattern mask. Neill and Walling (1981) found that this “before-disruption effect” occurred specifically when alternatives were featurally similar. In contrast, Experiment 1 of the present study found that precuing facilitated identification of unfamiliar stimuli composed of letterlike features, particularly when alternatives differed in only one critical feature. Contrary to Smith, Haviland, Reder, Brownell, and Adams (1976), composition of letterlike features is therefore not sufficient to produce the before-disruption effect. The before-disruption effect appears to occur when there is opportunity to represent the stimulus at a deeper (i.e., name) level, but foreknowledge of a critical distinguishing feature biases processing instead toward the level of physical features. Congruent with this analysis, Experiment 2 found the before-disruption effect for letters to be attenuated when targets were unpredictably upper- and lowercase, necessitating name-level matching to the alternatives. Experiment 3 found the superior identification of unprecued letters to be paradoxically associated with inferior target detection, as indicated by concurrent presence/absence judgments. In addition, identification of unprecued letters, but not precued letters, was significantly above chance on trials in which overt target detection failed to occur. The results are consistent with recent suggestions that pattern masking does not terminate perceptual processing, but rather interferes with conscious awareness of completed visual analysis.     

Visual pattern recognition: Size preprocessing re-examined

Template theories of visual pattern recognition assume the operation of preprocessing routines to deal with irrelevancies such as discrepancies in stimulus size. In three experiments where size was an irrelevant dimension, observers classified pairs of forms as either “same” or “different”. In Experiment I, the classification “different” was required when the stimuli shared the same form but a different orientation, and “same” when the stimuli shared the same form and orientation. Under these conditions RT was an increasing function of the magnitude of the size disparity between stimuli with equal slopes for “same” and “different” judgements. In Experiment II, “different” classifications were made to stimuli that had different forms, and “same” to figures with the same form. This stimulus set produced a size disparity function that interacted with response type; “different” responses had a shallower slope. Experiment III consisted of a mixed stimulus set drawn from both Experiment I and II. Stimuli that produced additive effects of size disparity and response type in Experiment I now produced an interaction between these two factors similar to the one observed in Experiment II. The results of these experiments are interpreted as evidence that previous contradictory results reported in the literature stem from differences in the way the stimulus set is constructed, and that size transformations can not be a necessary operation, at least when “different” judgements are made. The results are problematic for the view that size disparity effects in matching tasks are easily interpretable in terms of a primitive size normalization stage that precedes any comparison operations.     

Memory for scenes: Refixations reflect retrieval

Most conceptions of episodic memory hold that reinstatement of encoding operations is essential for retrieval success, but the specific mechanisms of retrieval reinstatement are not well understood. In three experiments, we used saccadic eye movements as a window for examining reinstatement in scene recognition. In Experiment 1, participants viewed complex scenes, while number of study fixations was controlled by using a gaze-contingent paradigm. In Experiment 2, effects of stimulus saliency were minimized by directing participants' eye movements during study. At test, participants made remember/know judgments for each recognized stimulus scene. Both experiments showed that remember responses were associated with more consistent study-test fixations than false rejections (Experiments 1 and 2) and know responses (Experiment 2). In Experiment 3, we examined the causal role of gaze consistency on retrieval by manipulating participants' expectations during recognition. After studying name and scene pairs, each test scene was preceded by the same or different name as during study. Participants made more consistent eye movements following a matching, rather than mismatching, scene name. Taken together, these findings suggest that explicit recollection is a function of perceptual reconstruction and that event memory influences gaze control in this active reconstruction process.     

An analysis of confusion errors in naming letters under speed stress

Three subjects named six visually presented letters under two levels of speed stress. The obtained confusion matrices for each stress condition were fit by Luce’s choice theory, which provided measures of stimulus similarity and response bias. Speed stress produced proportional increases in pairwise similarity measures but had no systematic effect on response biases. In Experiment 2, the same three subjects named the same letters under two levels of stimulus quality and a constant response-time deadline. As with speed stress, degrading the stimulus produced proportional increases in pairwise similarity measures but had no systematic effect on response biases. In Experiment 3, two of the subjects participating in Experiments 1 and 2 named the six letters under conditions where the probabilities of the letters were unequal. The letters toward which the subject had been most biased in Experiments 1 and 2 were assigned low probabilities, and the letters toward which he was least biased were assigned high probabilities. The result of this manipulation was to completely reverse the ordering of the response bias parameters of the Luce choice model. It is suggested that the present methodology provides a means of validating as psychological constructs the parameters of various mathematical models of stimulus recognition.     

Feature similarity and feature bias in identification of visually presented letters

Reaction time IRT) to correct identification (ID) was measured for pairs of different letters presented on a memory drum. There were two types of lists. In Type I, visual and name similarity varied orthogonally at two levels. In Type II, one feature was constant at one level, while the other varied at two levels of similarity. For both types of lists, RT is a function of the feature that is more easily extracted from the stimulus. Relative vivaal and name modality biases were estimated, and name bias is relatively more salient than visual bias under these experimental conditions. Specific letters differ in the amount of feature processing required for correct ID and in the relative contribution of visual and name feature effects on this processing.     

The nature of standard control in children's matching-to-sample

In Experiment I, six preschool-aged children were given matching-to-sample training with two figures in which they were required to choose one of two comparison stimuli that was identical in shape to the standard stimulus. Following this training, they were given intermittent test trials in which a novel stimulus figure was substituted for the previously correct comparison stimulus. Five of the six subjects consistently chose the substituted stimulus during test trials. Experiment II replicated the findings of Experiment I with three other preschool-aged children. Experiment II also provided controls for the possibility that the subjects of Experiment I were selecting the substituted stimulus because of its novelty. The investigators concluded that eight of the nine subjects were exhibiting the type of control described by Berryman, Cumming, Cohen, and Johnson (1965) as S-delta responding.     

Reaction times and error rates for “same”-“different” judgments of multidimensional stimull

Each S indicated whether two successively presented rows of letters were “same” or “different.” Reaction times of the “different” response seemed to indicate that S examined the stimulus letters in a serial, self-terminating manner. However, the reaction times of the “same” response were not consistent with this model. Consequently, it was proposed that S employs simultaneously two distinct processes for comparing stimuli. One process would generate the “different” responses; the other process would generate the “same” responses. Most false “same” responses occurred when the two rows of letters differed minimally. Thus, the false “same” responses appear to result from a failure to detect the difference between the two stimuli. However, when S made a false “same” response, he was aware that he had done so. Therefore, it was suggested that only one of the two comparison processes failed to detect the stimulus difference.     

Subjective shortening in humans' memory for stimulus duration

Three experiments investigated memory for stimulus duration in humans using a modification of a delayed-matching technique previously used to study event memory in pigeons. In a session of 48 discrete trials subjects were presented with a sample stimulus (a 500-Hz tone with mean duration of 400 msec) then a comparison stimulus (the same duration as the sample, or longer or shorter), after a delay that was 1 to 10 sec in Experiments 1 and 2, and 2 to 16 sec in Experiment 3. After the comparison had been presented, subjects judged whether the sample and comparison had the same duration (a YES/NO decision, Experiment 1), or whether the comparison was longer, shorter, or of the same duration as the sample (Experiments 2 and 3). Overall, mean number of correct responses changed little with increases in the delay, but the change of number of correct responses with delay was markedly different on trials in which the sample and comparison were the same, the comparison was shorter, or the comparison was longer. In general, accuracy declined with increasing delay in the first case, remained constant in the second case, and increased when the comparison was longer than the sample. Examination of the types of errors made on the different sorts of trials (Experiment 3) suggested that the data were produced by two mechanisms: (1) subjective shortening of the sample as the delay between sample and comparison increased, and (2) a time-order error to respond that the sample was longer than the comparison. Overall, it appears that humans' working memory for duration exhibits a subjective shortening effect similar to that previously found in pigeons.     

注意和非注意条件下的整体和局部性质加工

以往关于整体和局部知觉的研究通常要求被试直接对出现在复合刺激整体或局部水平上的靶目标做反应,因此复合刺激与任务相关并被注意。该研究通过测量复合字母的整体和局部性质对随后出现的探测刺激的启动效应来研究在非注意条件下整体和局部性质加工的差异。实验一发现复合刺激的整体和局部性质对探测刺激产生负启动效应,但二者没有显著差异。实验二缩短了启动刺激与探测刺激之间的时间间隔,复合刺激的整体和局部性质对探测刺激都不再产生启动效应。在实验一、二中,当要求被试直接对复合刺激做反应时,其分辨局部性质的错误率都比分辨整体性质的错误率高。根据这些结果,讨论了在注意和非注意下的整体和局部性质加工的差异。     

Verbal recoding of visual stimuli impairs mentalimagetransformations

Two experiments were carried out to test the hypothesis that verbal recoding of visual stimuli in short-term memory influences long-term memory encoding and impairs subsequent mental image operations. Easy and difficult-to-name stimuli were used. When rotated 90 degrees counterclockwise, each stimulus revealed a new pattern consisting of two capital letters joined together. In both experiments, subjects first learned a short series of stimuli and were then asked to rotate mental images of the stimuli in order to detect the hidden letters. In Experiment 1, articulatory suppression was used to prevent subjects from subvocal rehearsal when learning the stimuli, whereas in Experiment 2, verbal labels were presented with each stimulus during learning to encourage a reliance on the verbal code. As predicted, performance in the imagery task was significantly improved by suppression when the stimuli were easy to name (Experiment 1) but was severely disrupted by labeling when the stimuli were difficult to name (Experiment 2). We concluded that verbal recoding of stimuli in short-term memory during learning disrupts the ability to generate veridical mental images from long-term memory.