Backward conditioning as an extinction procedure

In two conditioned suppression experiments, rats received Pavlovian forward defense conditioning in which tonal conditioned stimuli (CSs) terminated with the onset of scrambled grid shock unconditioned stimuli (USs). After this experience, the rats then received a Pavlovian backward conditioning procedure in which the same USs now terminated with the onset of the same CSs. Although the two experiments differed greatly in terms of CS and US parameters, number of forward and backward pairings, and in terms of the general techniques used to establish and measure the Pavlovian conditioned response (CR), the results of both experiments agreed in showing that backward conditioning can indeed weaken a CR based on forward pairings. The results also show that, under some conditions, the backward procedure can be at least as effective in weakening an established CR as the traditional CS-alone extinction procedure; but, under other conditions, the backward procedure is less effective and leads to more spontaneous recovery than the CS-alone procedure.     

The effects of single-component extinction of a three-component serial CS on resistance to extinction of the conditioned avoidance response

Central to a fear interpretation of how avoidance responses are maintained in the absence of further CS-UCS pairings is the underlying assumption of an existing gradient of fear across the CS-UCS interval. Extrapolations based on this gradient lead to a number of differential predictions concerning the topography of avoidance responding during extinction. The present research was concerned with the differential effects of extinguishing separate components of the CS complex upon responding to the complete CS complex during extinction. In Phase 1 of the study, rats were classically conditioned to a three-component serial CS (S₁/S₂/S₃) followed by shock. Each subject was then given avoidance training in a one-way apparatus to a criterion of one successful avoidance. In Phase 2, subjects were divided into four groups, with three of the groups receiving nonreinforced exposure for 25 trials to one of the components of the serial CS (S₁, S₂, or S₃). The fourth group (S₀) was exposed for the same period of time to the apparatus cues. In Phase 3, the total stimulus complex was reintroduced in its original order, and animals were tested until extinction of the instrumental response was reached. The results are consistent with the hypothesis that a fear gradient exists in extinction and decreases in magnitude as the distance from the point of UCS onset increases.     

Phonetic recoding and reading difficulty in beginning readers

The results of a recent study (Liberman, Shankweiler, Liberman, Fowler, & Fischer, 1977) suggest that good beginning readers are more affected than poor readers by the phonetic characteristics of visually presented items in a recall task. The good readers made significantly more recall errors on strings of letters with rhyming letter names than on nonrhyming sequences; in contrast, the poor readers made roughly equal numbers of errors on the rhyming and nonrhyming letter strings. The purpose of the present study was to determine whether the interaction between reading ability and phonetic similarity is solely determined by different rehearsal strategies of the two groups. Accordingly, good and poor readers were tested on rhyming and nonrhyming words using a recognition memory paradigm that minimized the opportunity for rehearsal. Performance of the good readers was more affected by phonetic similarity than that of the poor readers, in agreement with the earlier study. The present findings support the hypothesis that good and poor readers do differ in their ability to access a phonetic representation.     

Levels, hierarchies, and the locus of control

The Bartlett--Craik view of human performance is restated; and particularly that it is organised at different levels. On that view, the lower levels are controlled by the upper but capable of functioning independently. Modern views of memory, language, and problem-solving are compared with this doctrine, and found to embody some of its virtues but not all. Fresh experiments are described, in which people take decisions about the running of a transportation system. The simplest control mechanism which will model their behaviour is a two-level adaptive controller.     

Orthographie distinctiveness of homonyms

Ratings of orthographic distinctiveness were obtained for 139 homonym pairs. Mean ratings on a 9-point scale ranged from 7.75 to 2.44. Reliability of the ratings was high (r = .91). In addition, orthographic distinctiveness was found to be independent of disparity in perceived meanings of the separate homonym forms.     

One-trial-a-day avoidance learning

A one-trial-a-day discrete-trial avoidance conditioning procedure run for 30 consecutive days was compared with a massed-trial procedure where Ss received 30 consecutive trials within 1 day. The Ss in both groups were equated for time each S spent in the nonshock compartment of the apparatus, number of times the transport box carrying Ss was lifted out of the nonshock compartment, and the number of times each S was handled. The main difference between groups was the intersession trial length of 24 h for the one-trial-a-day Ss. Learning was rapid for both groups. The groups did not differ reliably on six acquisition indices. The methodological advantages of the one-trial-a-day procedure and its theoretical importance were discussed.     

Perceptual masking: Peripheral vs central factors

Perceptual masking was studied under binocular and dichoptic conditions in order to separate peripheral and central interference effects. Under binocular conditions, when the test flash (TF) and the blanking flash (BF) fell on both retinas, both retroactive and proactive masking were demonstrated. Under dichoptic conditions, when the TF fell on one eye and the BF on the other eye, thus eliminating opportunity for intraretinal interference, there was partial retroactive perceptual masking and no proactive masking. These results suggest that binocular proactive masking is due to peripheral light adaptation, that binocular retroactive masking is due to both peripheral and central effects, and that dichoptic masking is due solely to central retrochiasmal interference. It is proposed that dichoptic retroactive perceptual masking affords a method of investigating central perception time, i.e., the time to consolidate a perceptual experience.