Book reviews

Animal Discrimination Learning. Edited by R. M. Gilbert and N. S. Sutherland. London: Academic Press. 1969. Pp. xvi + 501. 1358.

Luce, R. D. and Tukey, J. W. (1964). Simultaneous conjoint measurement: a new type of fundamental measurement. J. math. Psychol. I, 1-27.

Discrimination Learning. By D. A. Riley. Boston: Allyn and Bacon Inc. 1968. Pp. 172. Paperback 21s.

Annual Review of Psychology. Vol. 20. Palo Alto: Annual Reviews Inc. 1969. Pp. ix + 544. $9.00.

Cutaneous Sensation. By David Sinclair. London: Oxford University Press. 1967. Pp. xii + 306. 63s.

Modelling of Thinking and the Mind.. By N. M. Amosov. Translated by L. Finegold. New York: Spartan Books. London: Macmillan. 11967. Pp. xiii + 192.

The Mind of Mnemonist. By A. R. Luria. London: Jonathan Cape. 1969. Pp. xi + 160. 25s.

Determinants of Infant Behaviour IV. Edited by B. M. Foss. London: Methuen. 1969. Pp. 303. £3 10s.

Brain and Behaviour. Volumes 1-4. Edited by Karl Pribram. Harmondsworth: Penguin Books Ltd. 1969. Pp. 496 +573 + 523 + 524. 12s. 6d. per volume.     

Syntactic structure modifies attention during speech perception and recognition

The present paper demonstrates the interaction of syntactic structure and speech perception with a response task which minimizes the effects of memory: reaction time (RT) to clicks during sentences. (1) In 12-word unfamiliar sentences each with two clauses, RT is relatively slow overall to clicks located at the end of the first clause but decreases as a function of clause length. Clicks at the beginning of the second clause are not affected by length of the preceding clause. (2) In familiar sentences, RT is relatively fast to clicks located at the end of a clause while RT to clicks at the beginning of clauses is relatively unaffected by familiarity. (3) RT is not fastest overall to clicks located between clauses either in novel or familiar sentences. (4) As in previous studies, the subject's subsequent judegment of the location of the click tone are towards the clause break. (5) We could find no systematic interaction between RT and subjective click location. Findings (1) to (3) are consistent with the view that perceptual processing alternates between attending to all external stimuli and developing an internal representation of the stimuli. Finding (3) is in conflict with an “information channel” view of immediate attention to speech, which would predict high sensory attention to non-speech stimuli between clauses. However, findings (4) and (5) indicate that the channel view of perception may be correct for that perceptual processing which occurs after the immediate organization of the speech stimulus into major segments.     

Are thresholds reduced by illusions? An attempt at replication

Three experiments are reported, which are attempts to replicate the finding of Ross and Gregory (1964) that difference thresholds for weights can be lowered by means of the size-weight illusion. Three different procedures were used, the first one (experiment I) being designed to show whether or not changes in a subject's judgement criterion could account for apparent changes in sensitivity. The second method (Experiment II) was a replication of Ross and Gregory's first procedure, in which the standard weight was judged before the comparison. In Experiments I and II a larger illusion was induced than in the original studies, but in Experiment III both the weights and container sizes were practically identical to those used by Ross and Gregory. The procedure was also the same as their most successful procedure (number 3) in which standard and comparison were judged simultaneously. The findings were uniformly negative: there was no evidence of criterion shift when the size-weight illusion was induced nor did we find the lowering of threshold previously reported.     

Similarity of cardiac CR forms in the rhesus monkey during several experimental procedures

Cardiac rates of rhesus monkeys were observed in a variety of different conditioning procedures, each of which involved a visual stimulus (CS) followed by an electric shock (US). With a 30-sec CS, cardiac rate accelerated rapidly after CS onset, reached a maximum in the middle of CS, and decelerated thereafter, with a terminal CS rate often at the level of, or below, pre-CS levels. A similar biphasic cardiac rate response in CS was also observed under subsequent exposure to intermittent pairings of CS and US, avoidance of US, response-produced termination of US, and when CS-US pairings were superimposed upon an avoidance baseline, even when CS duration was varied from 12 to 60 seconds. The unusual regularity of cardiac rate responses in several different procedures may result from one or more of these factors: (a) characteristics of the rhesus monkey, (b) initial exposure to Pavlovian conditioning, or (c) the uniformity of measurement of cardiac rate employed in this study.     

Vibrotactile vigilance: The effects of costs and values on signals

Vibrotactile vigilance behavior was examined for the effects on signal detection performance of placing costs on misses and false detections and a positive value on the correct detection of a signal. Analyses over time showing that the frequencies of correct detection and false detection of signals decreased, while response times increased, indicated that increased costs for misses and false alarms lead to poorer correct detection performance, while the value placed on the correct detection of a signal had little effect. The d’ statistic of signal detection theory was invariant with both signal costs and time, while β varied with both factors.These results imply that the performance decrement during a vigil was due to an increased strictness in the criterion (β) the S set for deciding whether or not a signal was present. The cost factors were effective in manipulating performance during the watch by causing changes in the S’s decision criteria. Findings from this study clearly support those predicted by the “Decision Theory” of Swets, Tanner, and Birdsall (1961); this is suggested as perhaps being the best available basis for a theory of vigilance at this time.     

Temporal sequence effects in auditory oddity discrimination

The oddity method was used in assessing pitch, loudness, simultaneous tone, successive tone, and speech sound discrimination in 35 normal children and 15 children with learning problems. With this method three auditory stimuli are presented, two of which are identical, and the S is required to indicate the temporal position of the odd stimulus. For both groups, discrimination was most accurate when the odd stimulus was in the third position. These results could be explained by assuming that the oddity response was based upon successive Same-Different judgments of the first and second stimuli and the second and third stimuli, since a correct response to third-position oddity would require only a Same judgment of the first and second stimuli. Other findings were not as easily explained by this simple model, and alternative hypotheses are discussed.     

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