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.     

Retrieval time as a function of memory ensemble size

A direct test was performed of Oldfield's (1966) derivation of the relationship between naming response latency and memory ensemble size. The results confirmed Oldfield in every particular. Further, the results support Sperling's (1967) suggestion of a recognition buffer-memory mechanism between the initial stimulus-encoding stage and the long-term memory stage of human information processing.     

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.     

A three-electrode system for EKG recording and aversive shock

The use of three electrodes to produce digitizable EKG’s and to deliver shocks to the tail of the monkey is described. Cardiac signals are taken from a head electrode and a “ground” tail electrode. Shock is administered through a “hot” tail electrode and the “ground” tail electrode.     

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.     

The bioelectrical activity of cerebellar structures in the freely-moving rat

Electrodes were implanted in the brains of 27 freelymoving rats and the bioelectrical activity of cerebellar cortical structures (lobus simplex, tuber verrais, lobus ansiformis, crus II) and the dentate nucleus was measured simultaneously with the activity of the cerebral cortex and dorsal hippocampus and respiratory rate and motor activity. Different behavioral states were produced by habituation procedures and by elaborating conditional avoidance reflexes to light-flash or click series. In addition, startle reflexes to acoustic stimuli were used to evaluate behavioral state. The following conclusions could be drawn: 1) in the awake rat the various cerebellar structures have clearly distinguishable bioelectrical activity patterns; 2) changes in these patterns depend on the actual behavioral state of the animal; 3) this dependence upon behavior is especially clear in crus II, one of the projection zones of the tactile and proprioceptive afferent nerves in the cerebellar cortex. The changes in the electrocerebellogram of the unrestrained rat may be used as an indicator of the behavioral state of the animal.     

A titration procedure for generating escape behavior

In a grid-shock escape paradigm using time-out as reinforcement, both fixed-ratio and variable-interval performances were established directly from a continuous reinforcement schedule with rats and guinea pigs. A procedure was developed that employed a stepwise decrease in reinforcement time for all responses except the terminal response. Acquisition and long-term maintenance data were obtained from Ss trained on this titrated negative-reinforcement procedure.     

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.     

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.