The effect of change in sequential visual stimuli on GSR adaptation: II,the novel stimulus as a disinhibiting stimulus

GSR records were obtained for 20 Ss presented with a series of 80 stimuli (four lights alternating in apparent random sequence). Records were obtained, also, for 20 Ss in each of two groups, using the same procedure: in Group 1, a tone was substituted for one of the lights, early in the sequence, and in Group 2, it was substituted later in the sequence. The tone, the novel stimulus, produced significant changes in the GSR adaptation patterns of the two groups.     

Comparisons of memory for nonverbal auditory and visual sequential stimuli

Properties of auditory and visual sensory memory were compared by examining subjects' recognition performance of randomly generated binary auditory sequential frequency patterns and binary visual sequential color patterns within a forced-choice paradigm. Experiment 1 demonstrated serial-position effects in auditory and visual modalities consisting of both primacy and recency effects. Experiment 2 found that retention of auditory and visual information was remarkably similar when assessed across a 10 s interval. Experiments 3 and 4, taken together, showed that the recency effect in sensory memory is affected more by the type of response required (recognition vs. reproduction) than by the sensory modality employed. These studies suggest that auditory and visual sensory memory stores for nonverbal stimuli share similar properties with respect to serial-position effects and persistence over time.     

Stimulus novelty and intraseries primacy in GSR adaptation

GSR records were obtained for four groups of 20 Ss. Group I was presented with a series of four different lights (amber, blue, green, and white) appearing 20 times each, in apparent random order. The procedure was similar for the other three groups except that in group 2, a novel stimulus (a red light) appeared instead of the sixth amber light; in group 3, it appeared instead of the 16th amber light; and, in group 4, it appeared instead of the 16th amber light. Typical GSR adaptation phenomena were observed in all groups. The introduction of the novel stimulus appeared to have no effect on the course of GSR adaptation.     

Stimulus novelty and intraseries primacy in GSR adaptation

GSR records were obtained for four groups of 20 Ss. Group I was presented with a series of four different lights (amber, blue, green, and white) appearing 20 times each, in apparent random order. The procedure was similar for the other three groups except that in group 2, a novel stimulus (a red light) appeared instead of the sixth amber light; in group 3, it appeared instead of the 11th amber light; and, in group 4, it appeared instead of the 16th amber light. Typical GSR adaptation phenomena were observed in all groups. The introduction of the novel stimulus appeared to have no effect on the course of GSR adaptation.     

High familiarity enhances visual change detection for face stimuli

Does high familiarity with a face enable particularly efficient visual processing? In three experiments, we presented briefly and successively two pairs of faces (either famous or recently learned), masking each presentation. Between the first and the second presentations, one face changed, and the task was to locate this change. Performance was significantly better when the change involved a famous face. This superfamiliarity effect was found only for changes occurring in the left visual field and was abolished by inverting the faces. Extended prior study of the recently learned faces did not improve performance with these stimuli. The results suggest that superfamiliarity promotes highly efficient visual processing and may especially activate a configural mode of analysis.     

Effect of prior body experience on adaptation to visual displacement

The effect of proprioceptive adaptation to visual displacement is to produce a violation of the normal constraints on the relative position of body parts. In order to investigate the effect of this violation of constraints on the adaptation, the relative position of body parts for a group of dancers and a group of nondancers was determined after 5 and 15 min of adaptation. Empirical and theoretical support were provided for the propositions that (1) there is a tendency to resist the violation of constraints, and (2) the nature of the adaptation process is such as to minimize the amount of violation of constraints.     

Effect of interval between auditory and preceding visual stimuli on auditory sensitivity

Auditory thresholds were determined by a modified method of limits, in introverts, ambiverts and extraverts, under three intensities of light. Five determinations were made: one before, one during and three (30 sec., c. 8 and 16 min.) after the light stimulation. An analysis of variance of the data showed significant results for the interval conditions, the personality type and the interaction of these parameters, under the weak light. Interval effects were also significant under medium and strong light. A weak light increased, and a strong light decreased, auditory sensitivity when threshold determinations began 30 sec., but not more than about 8 min., after the light stimulation, in introverts.     

Effects of postresponse visual stimuli on visual discrimination learning in the rhesus monkey

To learn more about the mechanism (or mechanisms) involved with postresponse stimulus processing during discrimination learning, a series of studies was conducted with monkeys to determine why the combined relevant and irrelevant stimuli impair learning more than irrelevant stimuli appearing alone. It was found that: (a) the greater size and complexity of the combination of stimuli were not responsible for the greater deficit, while the presence of the relevant stimuli (S^D and S^Δ) within the stimulus combination apparently was; (b) the more similar the postresponse irrelevant stimuli were to the relevant stimuli the greater the deficit that resulted; and (c) monkeys that had earlier learned to discriminate the relevant and irrelevant features of a combination showed no learning impairment when this same stimulus combination was later presented after the response during a new learning problem. These results were interpreted as evidence that: (1) processes associated with learning a discrimination problem do not end with the execution of a choice response; (2) postresponse stimuli produce greater impairment in discrimination learning when they are distorted versions of the relevant stimuli; and (3) the impairment resulting from postresponse irrelevant stimuli occurs primarily when this misinformation is processed and misperceived as being relevant to learning the discrimination problem.     

Simultaneous vs sequential discriminations of Markov-generated stimuli

This experiment required Ss to make same-different classifications of Markov-generated histoforms that were distortions of three different prototypes. Task memory requirements were varied by presenting stimuli either simultaneously or sequentially for comparison, and the effects of shifts in memory requirements were also assessed. Classification performance in all cases was found to be superior under the simultaneous condition. Postshift performance was strictly a function of the mode of stimulus presentation following the shift, rather than the memory requirements present in the initial trials. These results, coupled with the observed relationships between performance and a measure of individual stimulus variability under the two memory conditions, strongly suggest that prototype encoding has limited relevance to performance in the same-different classification task used here.     

Detection of visual stimuli in correlated noise

The hypothesis of detection by temporal probability summation (TPS) as characterised in Mortensen [(2007). An analysis of visual detection by temporal probability summation, submitted for publication] is critically evaluated, considering data from an experiment of Roufs and Blommaert [(1981). Temporal impulses and step responses of the human eye obtained psychophysically by means of a drift-correcting perturbation technique. Vision Research, 21, 1203-1221], who derived the impulse and the step response for a sustained type of channel. The assumed approximate linearity of the channel is discussed with respect to recent findings from neurophysiological investigations. The data are shown not to be compatible with the TPS-postulate. Further, a model of a cell assembly, consisting of a homogeneous set of neurons, is presented that allows for a natural interpretation of random fluctuations in case of temporal peak detection (TPD). The model may be discussed with respect to TPS as well as to TPD; in any case, the model allows to integrate some results concerning the effects of attentional focussing on the detection process.     

Selective adaptation effects on end-point stimuli in a speech series

Recent experiments in speech perception using the selective adaptation paradigm have found that the phonetic boundary of a test series shifts following adaptation. However, no changes within the phonetic category have been found. In the present experiment, a series of voiced CV syllables which varied along the feature of place was used in a selective adaptation paradigm. The end-point stimuli trom the test series were used as adaptors. Subjects used a 6-point rating scale to respond to the stimuli instead of the usual two-category identification. The average rating for end-point stimuli from the same category as the adaptor, as well as the boundary stimuli, shifted as a function of adaptation. In all cases, the average rating response shifted toward that of the unadapted category. The average rating for stimuli in the opposite category from that of the adaptor remained relatively unchanged. These results indicate that the entire category of the adapting stimulus changes as a function of selective adaptation and that the effect is not confined to stimuli near the phonetic boundary.     

Range estimates of distant visual stimuli

Os made magnitude estimations of the range of visual targets located at physical distances from a few hundred yards or less to more than 5 miles. The targets were at different elevations in different experiments so that O’s gaze varied from 0 to 90 deg. The targets were presented against the empty sky or against water. The Os were stationary in most experiments, but were in motion in one. Results show that the psychophysical functions are power functions whose exponents range from ca. 1.25 to 0.8, depending on the angle of the target above the horizontal. Background texture or O motion had no effect.