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.     

The speed of visual processing in children and adults: Effects of backward and forward masking

Children, 4-5 and 9-10 years old, and college-age adults were tested on two visual masking tasks. The first task required the Ss to identify whether a tachistoscopically presented bar was horizontal or vertical The second task, also using tachistoscopic presentation of stimuli, required Ss to locate a horizontal (or vertical) bar in a matrix of vertical (or horizontal) bars. In both tasks, backward masking produced greater disruption than did forward masking, and the amount of disruption induced by both backward and forward masking decreased as age increased. An Age by Masking Condition interaction was found only in the location task and reflected a much greater difference between backward- and forward-masking conditions for the youngest group than for the older groups. On the basis of these findings and other considerations, it was concluded that only in the location task, which presumably required visual search, was the speed of visual processing slower in the younger group.     

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 effect of part sequence on succession threshold

When letters of the word POT and the nonsense syllable OTP are presented in a typical orientation (horizontal) and a typical order (left to right, up to down), succession threshold is lower relative to presentation in an atypical orientation (vertical) and an atypical order (right to left, down to up). These results are interpreted as showing that learning to read English establishes both orientation and order parameters of a hypothetical analysis operation     

Effects of a conditioned reinforcer upon accuracy of match-to-sample behavior in pigeons

Three pigeons were trained to perform a two-key sequential match-to-sample task. During baseline conditions, food reinforcement was contingent upon the first match response to occur following 8-min periods, and orange illumination of both keys preceded the delivery of food by 0.5 sec. The baseline schedule of food reinforcement was in effect throughout the study. In some conditions, a 0.5-sec flash of orange keylight alone was presented contingent upon mismatch responses that followed variable time periods averaging 1 min. Rate of mismatch responses increased and accuracy of matching performances decreased as compared with baseline conditions. The ability of the 0.5-sec orange flash to reinforce mismatch responses was markedly reduced when it no longer immediately preceded the delivery of food.     

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.