The effect of memory load on reaction time in character classification

In order to investigate the effect of memory load on reaction time (RT), choice RT trials were embedded in a binary character classification task using the varied set procedure. Twelve Ss performed in experimental blocks, as well as in control blocks consisting of character classification trials only. In experimental blocks, every trial began as a classification trial with the presentation of a new positive set. On a random half of these trials, however, a choice RT stimulus was presented instead of a probe letter and S simply made the indicated response. Results indicated that memory load had no effect on the choice RT trials. Embedding choice RT trials in the classification task affected the intercept (but not the slope) of the function relating classification RT to memory load. This result implies that the increase in latency usually obtained in classification experiments is entirely due to an increase in the duration of the memory searching stage of processing.     

Visual angle and apparent size of objects in peripheral vision

Measurements of apparent size were obtained by distance adjustment of a peripherally viewed stimulus to produce a match to a foveally viewed standard. As eccentricity increased, the peripheral stimulus was adjusted at distances of progressively greater visual angle, indicating that a continuous diminution in apparent size occurs with increased eccentricity. This effect was found to be stable for several conditions of illumination and for changes in the light adaptive state of S. Apparent size diminution and apparent distance increase were also found for familiar objects viewed in an open field.     

Magnitude production and magnitude estimation of taste intensity

Magnitude productions of sodium chloride (salty), quinine hydrochloride (bitter), and sucrose (sweet) yielded steeper psychophysical functions than those obtained with magnitude estimation. Hydrochloric acid (sour) produced the opposite effect. The results are discussed with respect to previous findings in taste intensity scaling and to general psychophysical considerations.     

Inverse relation between choice and local response rate with a schedule of response-produced blackouts

Pigeons were exposed to a two-key concurrent chains schedule in which identical frequencies and distributions of food presentations generated different response rates in the terminal links. An inverse relation between local rate of response in the terminal links and relative frequency of response in the initial links was observed. The high response rate was produced in one terminal link by a second-order schedule in which responding produced brief blackouts of the response key. Responding under the same schedule in the other terminal link did not produce blackouts. Under initial training and after spatial reversal of the terminal-link schedules, two of three pigeons had lower relative frequencies of response in the initial member of the chain with the higher terminal link response rate. The third pigeon showed no change in preference at reversal.     

Two temporal parameters of food postponement

Rats were trained to press a lever under schedules of food postponement. In the absence of lever presses, food was delivered periodically (food-food interval). Responses initiated a second interval (response-food interval) that was reset by each additional response. Performance was first studied at different response-food intervals with the food-food interval fixed at 30 or 60 sec, or 10 min. Response-food intervals were examined in ascending order and then recovery was studied at shorter intervals. Finally, the food-food interval was manipulated with response-food interval fixed at 30 sec. At food-food intervals of 30 and 60 sec, responding first increased and then decreased as the response-food interval increased. At the 10-min food-food interval, responding decreased with increasing response-food interval. In general, very low rates of responding occurred when the response-food interval was 60 sec or more and when it equalled or exceeded the food-food interval. However, responding was maintained in one animal when the food-food interval was decreased from 120 to 15 sec with the response-food interval at 30 sec. Results, in terms of several dependent variables, are compared with data on shock avoidance. Effects of response-independent and response-produced food and shock are discussed.     

Changing the response unit from a single peck to a fixed number of pecks in fixed-interval schedules

Each of three pigeons was studied first under a standard fixed-interval schedule. With the fixed interval held constant, the schedule was changed to a second-order schedule in which the response unit was the behavior on a small fixed-ratio schedule (first a fixed-ratio 10 and then a fixed-ratio 20 schedule). That is, every completion of the fixed-ratio schedule produced a 0.7-sec darkening of the key and reset the response count to zero for the next ratio. The first fixed-ratio completed after the fixed-interval schedule elapsed produced the 0.7-sec blackout followed immediately by food. These manipulations were carried out under two different fixed-interval durations for each bird ranging from 3 min to 12 min. The standard fixed-interval schedules produced the typical pause after reinforcement followed by responding at a moderate rate until the next reinforcement. The second-order schedules also engendered a pause after reinforcement, but responding occurred in bursts separated by brief pauses after each blackout. For a particular fixed-interval duration, post-reinforcement pauses increased slightly as the number of pecks in the response unit increased despite large differences in the rate and pattern of key pecking. Post-reinforcement pause increased with the fixed-interval duration under all response units. These data confirm that the allocation of time between pausing and responding is relatively independent of the rate and topography of responding after the pause.     

Schedule control of the vocal behavior of Cebus monkeys

The vocal behavior of three Cebus monkeys was maintained by fixed-ratio schedules of response dependent reinforcement at values between fixed-ratio 1 and fixed-ratio 15. In one monkey that was exposed to variable-interval, fixed-interval, and conjunctive fixed-ratio fixed-interval schedules of reinforcement, vocal responding occurred at a low rate, but schedule-appropriate patterns were maintained. The rates and patterns of responding engendered indicated that the vocal operant can be brought under schedule control in the monkey by the use of response-dependent reinforcement.     

Preference for locus of punishment in a response sequence

Food-deprived pigeons pecked a key under a schedule in which grain was made available after the seventieth peck. In each sequence of 70 responses, either the first, middle, or final response was followed by electric shock. Before the first response of each sequence, each response on a second key changed the color of the food key and the schedule of shock that was correlated with the food key color. Each pigeon preferred a schedule of shock, in that each of the three shock schedules did not occur equally often. The preferred shock schedule and the strength of the preference varied among the pigeons. The overall rate of responding by a pigeon under a given shock schedule was directly related to the pigeon's relative preference for that schedule, except when shock after the first response in the sequence was the most preferred schedule.     

A method for the precise switching of speech

A simple procedure by which a speech signal may be switched on or off (or from one ear to the other) at a precise instant of time is described. The speech sample is first recorded on a magnetic tape loop. A reference pulse is then recorded preceding the speech signal. This reference pulse triggers an adjustable time delay which in tum operates an electronic switch at an appropriate time.