Control of movement patterns in animals

As a more junior Fellow of the same college in Cambridge as Sir Frederic Bartlett, I am especially glad of this opportunity to join with members of the Experimental Psychology Society in honouring him. It would be superfluous for me to speak here of Sir Frederic's academic achievements: so many of our members are engaged in research on problems which sprung from his pioneering work, and his influence on the development of psychology as a science certainly needs no elaboration by me. But I would like to make one personal remark. I suppose all younger men feel that there are just a very few members of the preceding generation who have achieved a stature which will always be beyond the reach of any of their own contemporaries. Sir Frederic has always been one of those for me. I am speaking here not only of his academic achievements, but of his kindness as a man; and I would like to tell him how much I valued his willingness to share some of the benefits of his experience when I was blundering about on the borders of his subject.     

Frequency discrimination near masked threshold

Frequency DLs (Δf) at 1000 Hz were obtained in quiet and under masking conditions similar to those used in pitch-shift experiments, narrow-band noise at levels of 60, 80, and 100 dB SPL and tones at 15 dB SL or less. The Δfs were obtained by means of a tracking task in which the S controlled the input voltage to a frequency modulator. Characteristic improvement was seen when Δf was plotted as a function of sensation level. However, noise level itself was a significant factor, with more intense noise resulting in larger Δfs for tones of equal sensation level re masked threshold. This departure from previous findings is attributed to the signal and noise levels used, although the possibility exists that it is due to the use of modulated tones.     

Similarity judgments of line length

Nine Ss judged similarity of pairs of lines on a scale from 0 to 100, and 14 Ss made magnitude estimations of similarity of pairs of lines. The two scales of similarity were linearly related. Scale values for subjective length were obtained in one dimension using a nonmetric multidimensional analysis. Subjective length was found to be logarithmically related to objective length, and similarity was found to be an exponential     

Recency discrimination predicted from absolute lag judgments

An experiment is described which tests the plausibility of the assumption that two-alternative forced-choice (2AFC) recency discrimination is based on an independent lag estimate of each item. 39 Ss made absolute recency judgments for items (common nouns) at varying lag intervals while an independent group of 74 Ss made 2AFC judgments for pairs of items at comparable lag combinations. It was found that the absolute judgment data generated accurate predictions of 2AFC performance.     

The relationship between cognitive,motor-kinesthetic,and oculomotor adaptation

The literature concerning adaptation to prism indicates that several adaptive mechanisms may be important. The particular mechanism or mechanisms involved depends (at least in part) upon the type of adaptive exposure. In the present study. three adaptive mechanisms (cognitive. oculomotor, and motor-kinesthetic) were investigated. Ss were asked to point in the dark at an illuminated target. The target was seen displaced from its veridical position due to a wedge prism placed before S’s right eye. The left eye was occluded. Ss then viewed their visual target pointing errors through the displacing prism without seeing any part of their bodies. One group of Ss was instructed to ignore these prism-induced errors and to continue pointing at the target’s visual position. A second group of Ss was instructed to compensate fully for their errors and to at tempt to eliminate them on all future trials. For the latter group errors were completely eliminated, while for Ss instructed to ignore their errors, relatively small improvement in visual target settings occurred. This improvement was called cognitive adaptation, since it depended on the S’s conscious control. In addition. for both conditions. evidence was found that allowing Ss to view their prism-induced pointing errors resulted in some form of motor-kinesthetic adaptation. This adaptation was hypothesized to represent a change in the judged position of the pointing hand relative to its felt position. It was concluded that this motor-kinesthetic adaptation was dependent, in part, upon cognitive information concerning the effects of the prism and that it serves to reduce conflict between cognitive and visual cues, i.e., between what S believes and what he sees.     

Individual half-judgment brightness functions

Nine Ss made half-judgments of each of nine brightness standards. Individual half-judgment brightness functions were constructed, one for each of the two threshold forms of the power law. The ω-Law (translation on the psychological axis) provided a better fit to the half-judgment data than did the ?-Law (translation on the intensity axis). A test of scale consistency for the fractionation method was confounded with the power law hypothesis, but the data are interpreted as providing fair support for the method independent of the form of the power law. The effect of Standard on exponent estimates was significant for both forms of the law, and the effect of Standard on threshold estimates was significant for the ?-Law but not for the ω-Law. Both forms of the law contain a so-called threshold parameter, but the interpretation of this parameter as a threshold was rejected for the ?-Law and accepted for the ω-Law.     

A note on chaining and temporal discrimination

Four pigeons were exposed to a two-key DRL procedure. At the start of a trial, key A was illuminated. A response to the lighted key turned it off and simultaneously illuminated key B. Reinforcement was available for responses on key B which followed the initial key A response by more than 2 sec. In the course of exposure to these conditions, all birds acquired superstitious response chains on key A. The distribution of the number of responses on key A preceding a key B response and the distribution of intervals elapsing from the initial key A response to the key B response were of the same form. The suggestion is made that the superstitious responding on key A served to mediate the required delay interval. However, when intervals between successive key A responses were recorded for one subject, they were found to be regularly spaced in time. Thus, the problem remains of how this behavior is itself timed.