Word and nonword superiority effects in a letter detection task

Subjects searched for predesignated consonant letters embedded in strings of consonants, consonants and vowels, or consonants and numbers. In Experiments 1-3, detection was quicker in the consonant-vowel and consonant-number strings than in the consonant strings. Apparently, vowels and numbers were less confusable distractors than are nontarget consonants. Experiment 4 tested whether psychophysical or categorical information about letters and numbers enabled subjects to process consonant-vowel and consonant-number strings more quickly. Results indicated that psychophysical characteristics of target and distractor letters mediated both word and nonword superiority effects.

     

Differences in the search rate of children and adults in short-term memory

When people recognize a test item as belonging or not belonging to a previously presented set, recognition latency increases with the number of items in the set. Although some evidence suggests otherwise, it is currently held that the rate of this increase is the same for children and adults. In contrast, the present experiments indicated a much slower search rate for second graders (mean age = 7.33 years) than for seventh (mean age = 12.50 years) and twelfth graders (mean age = 17.25 years). Moreover, search rate for second graders was invariant under instructions which did or did not emphasize speed and with presentation of the memory set in either the auditory or visual modality. Experiment II showed that the slow search rate for children was not due to differences in encoding between children and adults.     

Two kinds of adaptation in the constancy of visual direction and their different effects on the perception of shape and visual direction

Adaptation in the constancy of visual direction can be obtained under two radically different conditions, called eye-movement adaptation and field adaptation. Adaptation resulting from these conditions and from a “normal” condition was measured with a newly developed estimation test. Eye-movement adaptation was found to cause an alteration of compensatory eye movements. It apparently consists of a changed evaluation of eye movements, as demonstrated by two different pointing tests. A form test where the shape of a large oblong is set to look square also confirmed this interpretation. After field adaptation, a pointing test did not register a change, but an adaptation effect could be measured with a forward direction test. This test and a square test where no eye movements were permitted proved to be specific to field adaptation; they measured no effect after eye-movementadaptation. The normal adaptation condition Was apparently equivalent to the eye-movement adaptation condition. Its effect could be measured only with a pointing test. When we changed the normal adaptation condition so that frequent saccades were made during head turning, strong effects were measured with the two tests that were specific to field adaptation.     

Stimulus and response factors in mirror-image discrimination

Two choice-reaction time studies assessed the influence of stimulus-response mapping, stimulus complexity, and stimulus alignment on adults’ discrimination of mirror-image and nonmirror-image stimulus pairs. Half the subjects in Experiment 1 were instructed to treat nonmiiTor pairs as “same” and mirror pairs as “different”; the other half responded in the opposite manner. The first group responded more quickly to nonmirror pairs, while the second group responded more quickly to mirror pairs. This result, which held for horizontal stimuli (side by side) as well as for vertical stimuli (one above the other), confirms the importance of experiential factors in mirror-image “confusions. “ In Experiment 2. stimuli were drawn from a population of patterns whose complexity could be objectively defined. In general, the more complex the pattern, the slower the response and complexity seemed to influence the qualitative nature of pattern processing. In both experiments, subjects responded more quickly to horizontal stimuli than to vertical stimuli.     

Crowding: Effects of Group Size,Room Size,or Density?

The separate effects of group size, room size, and density (space per person) were investigated for subjects responding interactively or coactively to perceptual and cognitive tasks. The major findings are that crowding has greater effects on "feelings" and "interpersonal perceptions" than on task performance. Where crowding did have effects, they appeared to be mediated more by group size and, to some degree, room size than by density, especially for males. Female subjects appeared somewhat more density oriented than male subjects.     

Invariance of the weight parameter in information integration

The relative effect of each informational dimension in an information integration task is a joint function of its weight and the range of values over which it is varied. A method is developed for separating these two factors. Weights obtained by this method were compared across variations of stimulus range. Subjects rated the performance of students on the basis of midterm exam scores and final exam scores. For some subjects, the range of scores on the final exam was twice that on the midterm and the reverse was true for other subjects. An averaging model was shown to describe the results, and weights did not differ for different stimulus ranges. This was true for each of two instructional conditions: one in which a particular weighting strategy was prescribed and one in which there was no prescribed weighting. Students who were instructed to use a 2∶1 weighting were found to assign more than twice as much weight to the final as to the midterm.     

Periodicity pitch perception and its upper frequency limit in cats

We have established a procedure for behavioral assessment of periodicity pitch perception in the cat. This procedure requires the training of cats to make a differential response to two different pure tones, and then testing for the transfer of learning when complex stimuli known to produce periodicity pitch sensations in humans are substituted for the pure tones. Complex stimuli consisted of three to five harmonically related frequencies of the same amplitude and phase. Eight cats were the subjects of these experiments. Two of them were controls. It is demonstrated here that cats do perceive periodicity pitch. We also used this procedure to measure the upper frequency limit of periodicity pitch perception for two cats. The frequencies tested were 100, 200, 300, 400, 600, 800, 900, and 1,200 Hz. The data indicate that the upper frequency limit of periodicity pitch perception in the cat is on the order of 600 to 800 Hz. There is a trend of decreasing prominence of the perception of periodicity pitch as the component frequencies are increased. These results are parallel to the human psychophysical data.