Within-session Changes In Responding During Concurrent Variable-interval Schedules

Five rats and 4 pigeons responded for food delivered by several concurrent variable-interval schedules. The sum of the rates of reinforcement programmed for the two components varied from 15 to 480 reinforcers per hour in different conditions. Rates of responding usually changed within the experimental session in a similar manner for the two components of each concurrent schedule. The within-session changes were similar to previously reported changes during simple schedules that provided rates of reinforcement equal to the sum of all reinforcers obtained from the concurrent schedules. The number of changeovers also changed within sessions in a manner similar to the changes in instrumental responding. These results suggest that changeovers are governed by the same variables that govern instrumental responding. They also suggest that the within-session change in responding during each component of a concurrent schedule is determined by approximately the sum of the reinforcers obtained from both components when both components provide the same type of reinforcer.     

用皮肤辨别颜色

绝大多数人是用视觉系统来辨别颜色的。但是,也有人能用手指辨认颜色。心理学家扎瓦拉(Zavala)、范科特(Van Cott)、奥尔(Orr)和斯莫尔(Small)对一个自称能用手指辨认颜色的人进行了广泛的研究并于一九六七年发表了研究结果。他们用多种作业让被试辨认。有一次让被试蒙住眼睛后对不同颜色的朴克进行分类。测查证明她是成功的,超过了简单猜测的水平;能够把红色和白色、红色和兰色区别开来,但不能区别兰色和白色。另外一次测试,她能确定在她手上是否有一道光照。照射到手上     

Impairment in the control of coupled cyclic movements of ipsilateral hand and foot after total callosotomy

Integrity of both cerebral hemispheres is required to control in-phase or anti-phase coupling of ipsilateral hand and foot oscillations, as shown by the impairment of these tasks when performed on the healthy side of hemiplegic patients. On this basis, coupling of hand–foot movements was analysed in a right-handed subject (ME) who underwent a total resection of the corpus callosum. Oscillations of the prone hand and foot, paced by a metronome at different frequencies, as well as EMG activity in extensor carpi radialis (ECR) and tibialis anterior (TA) muscles were analysed by measuring the average phase difference between the hand and foot movements and EMG cycles.

ME performed in-phase movements (right-hand extension coupled to right-foot dorsal flexion) at frequencies up to 3 Hz, though the hand cycle progressively lagged the foot cycle as the frequency increased. At 3 Hz the hand lag reached −142° (as compared to about 25° in healthy subjects). The lag increased even further after application of an inertial load to the hand, reaching 180° at 1.8 Hz (about 50° in healthy subjects). ME's hand lag is caused by the lack of any anticipatory reaction in hand movers. In contrast to healthy subjects, which activate the ECR earlier than the TA when the frequency increases, ME activated the ECR later than TA at all frequencies higher than 0.9 Hz.

Anti-phase movements (hand extension coupled to foot plantar flexion) were performed only upto 1 Hz in unloaded conditions. At 0.6 Hz, movements were in tight phase-opposition (3°), but at 1 Hz, the hand lag reached −34° because of a delayed ECR activation. After hand loading ME was unable to couple movements in anti-phase. In contrast, normal subjects maintain a tight anti-phase coupling up to 2.0 Hz, both with an unloaded or loaded hand. Similar deficits were observed by ME when performing in-phase and anti-phase coupling on the left side, as well as when he was blindfolded.

In normal subjects, an anticipated muscular activation of hand movers compensates for hand loading. Since this compensation must depend on monitoring the hand delay induced by loading, the absence in ME of such compensatory reaction suggests that callosal division had apparently compromised the mechanisms sustaining feedback compensation for differences in the biomechanical limb properties. They also confirm and reinforce the idea that elaboration of the afferent message, aiming at controlling the phase of the movement association, needs the co-operation of both cerebral hemispheres.