The structure of visual pattern associates and pattern goodness

Two tasks were used with a total set of 126 dot patterns. In one task Ss rated the goodness of each pattern. In another task they produced a dot pattern as an associate to each of the patterns used as a stimulus. The distributions of the associates suggest that the total set of patterns is both partitioned and nested. Groups defined by rotation and reflection are partitioned, thus kept intact. These groups in turn form a series of nested subsets., Both partitioning and nesting produce subsets of different size. The size of these subsets is related to pattern goodness, with good patterns coming from small subsets.     

Influence pattern effectiveness

Managers apply different influence tactics to get subordinates to perform their tasks. For a better understanding of the influence process dynamics, it has been recommended to consider the combination of different tactics instead of analyzing them separately. (Cialdini & Goldstein, 2004). The present study has analyzed the effectiveness of various influence tactics combinations used by superiors with their subordinates. We identified four influence patterns: hard pattern, rational pattern, active pattern and passive pattern. Pattern effectiveness was analyzed in terms of subordinates' satisfaction, commitment and well-being. We found that superiors who used a broader range of tactics were more effective than those using a single range of tactics. Practical implications are discussed.     

Composition as pattern

Philosophical Studies - I argue for patternism, a new answer to the question of when some objects compose a whole. None of the standard principles of composition comfortably capture our natural...     

The temporal course of visual pattern encoding: Effects of pattern goodness

Subjects typically display superior reproduction of good (redundant, symmetrical) visual patterns compared with poor ones. This pattern goodness effect could conceivably involve encoding processes, short-term memory processes, or response processes. The present experiments explored the time course of wholistic encoding of Garner dot patterns as a function of tachistoscopic exposure time, delay of backward masking, and post-mask shadowing. Within the specific framework of additive factors theory, Experiment I showed: (a) equal rates of encoding for all patterns since comparable slopes were obtained for the recall X processing time functions; and (b) superior absolute recall for good patterns since different intercepts were obtained. Experiment II demonstrated that when degree of encoding was initially equalized for all patterns, the rate of extraction of further information remained constant over available processing time and was unaffected by pattern goodness, slopes and intercepts for good versus poor patterns then being equal. Experiment III confirmed that, given some fixed duration of available processing time, information is abstracted at the same rate for all pattern regardless of the ratio stimulus display time to delay of mask onset. Experiment IV indicated that maintenance rehearsal normally occurs in the present experimental situation, and that very good patterns are somewhat less disrupted by shadowing over a three-second interval. While STM is thus implicated in the pattern goodness effect it does not follow that STM constitutes a complete explanation of the intercept differences reported here. Empirical evidence of response bias toward production of good patterns, however, was not found. It was shown that very good patterns are highly familiar and nameable, and proposed that they do consequently have an early encoding advantage.     

Spatial pattern learning in rats: control by an iterative pattern.

Rats searched in a matrix of vertical poles for food hidden on top of the poles. The only information available about the location of the food was the consistent spatial pattern of the baited poles, which was a checkerboard. This spatial pattern of hidden-food locations came to control the choices of poles made by the rats. The experiments ruled out the possibility that this control can be explained by the acquisition of simple response tendencies to move from pole to pole. Instead, this behavioral control of choices was attributed to the development of a representation of the checkerboard pattern of baited locations. Spatial pattern learning may have mechanisms in common with other forms of pattern learning.     

Discrete internal pattern representations and visual detection of small changes in pattern shape

A scheme is proposed that relates the internal representation of pattern stimuli to visual pattern discrimination performance. The main assumptions of the scheme are: (1) internal representations are assigned to patterns probabilistically; (2) internal representations are discrete; (3) visual discriminability of two patterns is determined by the differences in the assignment probabilities of their internal representations. It is suggested that the internal representations associated with a pattern may be analyzed by measuring the visual detectability of small changes in pattern shape at points along a continuum of shapes. This continuum is generated by a group of transformations smoothly parameterized by a single variable. In two experiments designed to test this approach, subjects discriminated pattern displays containing combinations of three-dot subpatterns. Under the hypothesis that there were just two relevant internal representations, specifying dot collinearity and dot noncollinearity, the qualitative characteristics of the discrimination performance were correctly predicted.     

Irrelevant relations and the active search for pattern structure in rat serial pattern learning

Hersh (Mem Cogn 2:771–774, 1974) investigated the role of irrelevant relations in college students’ pattern learning and performance for letter series completion problems. He created irrelevant relations in sequences by inserting items to make pattern structure ambiguous such that it was open to multiple interpretations during initial pattern processing. He reported irrelevant relations impaired humans’ performance more when placed at the beginning of patterns than at the end. However, once pattern structure was induced, irrelevant relations were not impairing. Here, we examined the impact on rat serial pattern learning of irrelevant relations positioned at the beginning or end of a serial pattern. Rats pressed levers in a circular array according to the same structured serial pattern, 123 234 345 456 567, where digits indicated the clockwise position of the correct lever. This structured serial pattern was interleaved with repeating responses on lever 2 to produce irrelevant relations at the beginning of the pattern (Beginning: 122232 223242 324252 425262 526272), on lever 6 to produce irrelevant relations at the end of the pattern (End: 162636 263646 364656 465666 566676), or on lever 8 to produce no irrelevant relations (No Irrelevant Relations: 182838 283848 384858 485868 586878. Irrelevant relations significantly retarded learning regardless of their placement within the pattern. However, irrelevant relations retarded learning significantly more when placed at the pattern beginning versus end. The results indicate that rats, like humans, process patterns from beginning to end.     

Vibrotactile pattern isolation/integration

Temporal integration has been cited as a major factor in temporal masking. Two experiments were designed to examine the conditions under which temporal integration may aid or hinder the perception of vibrotactile spatial patterns. In Experiment 1, the subject’s task was to discriminate between pairs of patterns. Each pattern was composed of two temporally separated pattern elements. When the task required the subjects to perceive the individual pattern elements, performance improved with temporal isolation—that is, performance improved as the temporal separation between the elements increased. In a second task, when the discrimination could be based on either the overall pattern shape or the pattern elements, temporal integration appeared to improve performance—that is, performance improved as the temporal separation decreased. In Experiment 2, an identification task was used. Several factors appeared to determine whether temporal integration aided or hindered pattern identification. When pattern elements similar to those in Experiment 1 were tested, performance improved with increasing temporal separation (isolation). A single function was fit to the discrimination (isolation) and identification (isolation) results. Whether temporal integration aids or hinders pattern perception appears to depend on pattern shape, the pattern elements, and the nature of the task.     

文化模式中的宗教

伴随文化学、人类学、民俗学、宗教学、宗教社会学、宗教历史学等新兴交叉学科的诞生,对宗教的研究和把握已经走出原有的神学和宗教哲学视域,人们开始自觉地把宗教现象置于人的文化世界和现实生活世界之中加以把握,并积累了大量有价值的宗教问题的研究成果,这些理论成果为我们揭开许多历史之谜和破解各种关于宗教的神话提供了有益的启示.但是,宗教作为一种极为重要的文化形式在人类生活的自觉文化模式中究竟扮演着什么样的角色还不甚清晰,需要从理论上加以探讨.本文力求从人的生存活动和人的本性等维度探讨宗教的地位和价值,进而探讨宗教在文化模式的作用机制.     

Noise methods in pattern perception

This experiment investigated 4 methods of inducing visual noise at 7 levels of noise. Fortysix Ss were presented 4800 sets of 3 pattems, with the task of judging which of 2 noisy patterns was more similar to the prototype pattern. The noisy patterns were generated by adding, moving, deleting or both adding and deleting elements of the prototype. All possible comparisons of each noise method were made at each noise level and the results plotted. The results show that the various methods of introducing noise do not produce identical results, and that the similarity assessment is dependent on noise koel. Explanations are offered to account for the results.     

Modes of vibrotactile pattern generation

Two modes of generating vibrotactile patterns, static and scanned, were examined. In the static mode, all elements making up the pattern were turned on and off simultaneously. In the scanned mode, the pattern to be identified was moved across the tactile array. The patterns were letters of the alphabet presented to the fingertips by means of the Optacon, a reading aid for the blind. The results of the first experiment showed that the performance on a letter recognition task decreased as pattern duration decreased and that at all durations below 200-msec performance in the static mode was better than in the scanned mode. Good letter recognition was possible at durations of 4 msec in the static mode. The results of the second experiment showed that letter recognition in the static mode was highly dependent on the perceived intensity of the letters presented, whereas intensity changes in the scanned mode had little effect on letter recognition. The results of the third experiment showed that both modes of pattern presentation produced similar results in the presence of masking stimuli. The implications of the results for cutaneous pattern perception and information transmission and visual letter recognition are discussed.     

Temporal organization of pattern structure

Two pattern reproduction experiments examined the relations among the figural goodness of a pattern, the organization of two parts within the pattern, and the interpart interval (ISI), which ranged from 40 to 200 msec. If the parts contained connected line segments, performance was slightly better (3%-5% gain in accuracy) at a 40-msec ISI than at a 200-msec ISI. If the parts contained unconnected line segments, reproduction accuracy of the first part declined sharply between 40 and 200 msec. These results were interpreted by assuming that the parts were perceived as a single whole pattern at a 40-msec ISI but as two separate patterns at a 200-msec ISI. One surprising finding, the lack of an interaction between figural goodness and ISI, was explained in terms of a response bias in favor of figural good patterns. A secondary manipulation revealed that a part was more accurately reproduced in a good figure context than in a poor figure context but was most accurately reproduced when it appeared alone.     

Neural activation pattern in self-deceivers

While deception is a conscious cognitive effort and self-deception is an unconscious cognitive effort. Such effort possibly shapes the working memory and generates a neural activation pattern in self-deception. Little attempt was made to identify activation pattern in self-deception. The present study investigated the phenomenon of self-deception by increasing the working memory functions using a boxcar design. functional magnetic resonance imaging (fMRI) revealed more activation in bilateral inferior parietal lobule (BA 40), superior parietal lobule (BA 7), middle frontal gyrus (BA 9), medial frontal gyrus (BA 6), thalamus and cerebellum. Activated areas in frontal and parietal cortex suggest significant role of working memory during self-deception.     

Expertise in tactile pattern recognition

This article explores expertise in tactile object recognition. In one study, participants were trained to differing degrees of accuracy on tactile identification of two-dimensional patterns. Recognition of these patterns, of inverted versions of these patterns, and of subparts of these patterns was then tested. The inversion effect (better recognition of upright than inverted patterns) and the part-whole effect (better recognition of the whole than a part pattern), traditionally considered signatures of visual expertise, were observed for tactile experts but not for novices. In a second study, participants were trained as visual or tactile experts and then tested in the trained and nontrained modalities. Whereas expertise effects were observed in the modality of training, cross-modal transfer was asymmetric; visual experts showed generalization to haptic recognition, but tactile experts did not show generalization to visual recognition. Tactile expertise is not obviously attributable to visual mediation and emerges from domain-general principles that operate independently of modality.     

Eye-movement parameters and pattern discrimination

Pattern discrimination was studied in a visual-search task by recordingan O’s eye movements while he determined how many of eight patterns, arranged in a square around a standardpattern, matched the standard pattern. The results demonstrate the role of eye movements in visual search and human pattern discrimination. The mean duration of an eye fixation on a pattern, the probability of fixating it, the probability ofrefixating it, and the sequence in which patterns were fixated were all systematically related to various pattern measures. Multivariateanalyses showed modest correlations between the duration of individual eye fixations and various pattern measures. Relative characteristics of patterns influenced performance more than absolute characteristics of patterns. Patterns that matched a standard were fixated more often and longer than patterns that did not match a standard. The order in which patterns were fixated depended upon their relative characteristics. The results were consistent with a model ofpattern discrimination consistingoftwo stagesin which (1) features of a fixated pattern are abstracted and encoded, and (2) these features are then compared with the features ofanother pattern.