The symmetrical maze: An automated closed-field test series for rats

An automated “intelligence” test for rats is described. Supporting data indicate that this maze-problem series is sensitive to hypothyroidism-induced learning deficit and sex differences. Comparisons between this new problem set and the Rabinovitch-Rosvold (1951) closed-field tests are presented with respect to difficulty, internal consistency, and test-retest reliability.     

Book reviews

Encyclopaedia of Linguistics, Information and Control. Edited by A. R. Meetham with the assistance of R. A. Hudson. Oxford: Pergamon Press. 1969. Pp. xiv + 718. 300s.

The Biological Basis of Personality. By H. J. Eysenck. Springfield: Thomas. 1968. Pp. xv + 399. $18.50.

Scientific Basis of Dvug Dependence. Biological Council Symposium. Edited by H. Steinberg. London: Churchill. 1969. Pp. 429. 100s.

Minnesota Symposia on Child Psychology, Vol. 2. Edited by John P. Hill. Minneapolis: University of Minnesota Press. 1969. Pp. viii + 172.

Memory and Attention: an introduction to human information processes. By Donald A. Norman. Chichester, Sussex: John Wiley. 1969. Pp. ix + 201. 84s. (cloth); 44s. (paper). Verbal Learning and Memory: selected readings. By Leo Postman and Geoffrey Keppel. Harmondsworth: Penguin Books. 1969. Pp. 501. 12s.

Handbuch der Kinderheilkunde. Edited by H. Opitz and F. Schmidt. Rand VIII/I: Neurologie-Psychologic-Psychiatrie. Redigiert von F. Schmidt und H. Asperger. Berlin: Springer Verlag. Pp. 1060. Price DM385, S96.25.

Digital Computing. By R. S. Lehman and D. E. Bailey. London: John Wiley & Sons Ltd. 1969. Pp. xxiv + 303. 79s.

Real-Time Computers. By W. R. Uttal. New York: Harper & Row. 1968. Pp. xiv + 338. 93s.     

Signal probability and spatial location as possible bases for increased selectivity in noise

It was previously found that noise increased both performance on a primary tracking task and the detection of centrally located signals in a secondary multi-source monitoring task. The present experiment examines the effect of changing the distribution of signals across the monitoring display. When equal numbers are seen at all locations there is no differential effect of noise for central and peripheral locations. Such an effect only occurs when central signals are seen to have greater probability. This result points to the selectivity effect in noise being a function of task priorities and not of physical location.     

Visual on- and off-latencies and handedness

Ten Ss served in this experiment, five right-handed and five left-handed. Every S was tested in a perceived-order situation and by the up-and-down method to determine the relative on-latency for a visual test stimulus. i.e, (ON-Lat for lest stimulus involving right hemisphere- ON-Lat for standard stimulus involving left hemisphere) and to determine a similarly defined relative off-latency for the same test stimulus. The algebraic difference between the relative on-latency measure and the relative off-latency measure was then found. Data from a previous study had suggested that this “on-off difference” was characteristically positive for left-handed Ss and negative for right-handed Ss. The present data agree. The left-handed Ss were found to differ significantly from the right-handed Ss in the magnitude of the on-off difference. This outcome appears important as a possible clue to functional interhemispheric differences related to handedness.     

Selective eye movements to simultaneously presented stimuli during discrimination

Human Ss, when given a discrimination task whose stimuli varied in dimension and relevance, always chose and ftxated more frequently the stimulus they had been reinforced for choosing. Decreasing the brightness reduced the choice and ftxation preference for form stimuli over line stimuli and raised total ftxation frequency. Ss decreased fixation frequency to discriminanda with practice.     

The response-reinforcement dependency in fixed-interval schedules of reinforcement

Pigeons were exposed to four different schedules of food reinforcement that arranged a fixed minimum time interval between reinforcements (60 sec or 300 sec). The first was a standard fixed-interval schedule. The second was a schedule in which food was presented automatically at the end of the fixed time interval as long as a response had occurred earlier. The third and fourth schedules were identical to the first two except that the first response after reinforcement changed the color on the key. When the schedule required a peck after the interval elapsed, the response pattern consisted of a pause after reinforcement followed by responding at a high rate until reinforcement. When a response was not required after the termination of the interval, the pattern consisted of a pause after reinforcement, followed by responses and then by a subsequent pause until reinforcement. Having the first response after reinforcement change the color on the key had little effect on performance. Post-reinforcement pause duration varied with the minimum interreinforcement interval but was unaffected by whether or not a response was required after the interval elapsed.