Oculomotor and manual indexes of incidental and intentional spatial sequence learning during middle childhood and adolescence

The goal of this study was to examine incidental and intentional spatial sequence learning during middle childhood and adolescence. We tested four age groups (8-10 years, 11-13 years, 14-17 years, and young adults [18+ years]) on a serial reaction time task and used manual and oculomotor measures to examine incidental sequence learning. Participants were also administered a trial block in which they were explicitly instructed to learn a sequence. Replicating our previous study with adults, oculomotor anticipations and response times showed learning effects similar to those in the manual modality. There were few age-related differences in the sequence learning indexes during incidental learning, but intentional learning yielded differences on all indexes. Results indicate that the search for regularities and the ability to learn a sequence rapidly under incidental conditions are mature by 8 to 10 years of age. In contrast, the ability to learn a sequence intentionally, which requires cognitive resources and strategies, continues to develop through adolescence.     

Response Facilitation and Inhibition in Manual,Vocal, and Oculomotor Performance: Evidence for a Modality-Unspecific Mechanism

In 2 experiments (N = 10, Experiment 1; N = 16, Experiment 2), the authors investigated whether evidence for response facilitation and subsequent inhibition elicited by masked prime stimuli can be observed for output modalities other than manual responding. Masked primes were followed by target stimuli that required a 2-choice manual, saccadic, or vocal response. Performance was measured for compatible trials in which primes and targets were identical and for incompatible trials in which they were mapped to opposite responses. When primes were presented centrally, performance benefits were obtained for incompatible trials; whereas for peripherally presented primes, performance benefits were found in compatible trials. That pattern of results was obtained for manual responses and for saccadic eye movements (Experiment 1), demonstrating that those effects are not mediated by specialized dorsal pathways involved in visuomanual control. An analogous pattern of effects was found when manual and vocal responses were compared (Experiment 2). Because vocal responding is controlled by the inferotemporal cortex, that result shows that prime-target compatibility effects are not primarily mediated by the dorsal stream, but appear to reflect modality-unspecific visuomotor links that allow rapid activation of motor responses that may later be subject to inhibition.     

高血压患者应激反应特点及行为人格的关系研究

为了解高血压患者心血管反应的特征及与健康人群的差异,使用实验和问卷调查的方法对高血压患者和健康居民进行研究。结果显示,两组在任务期和恢复期的心血管反应差异显著（P〈0．05）;病例组的健康实践行为和消极应对方式水平较高,积极应对方式有待提升;健康实践行为和恢复期舒张压呈负相关,积极应对方式和任务期收缩压呈正相关（P〈0...     

高低创造性思维水平者的认知抑制能力：行为和生理的证据

本研究采用2个实验, 考察创造性思维测验得分高低者在Stroop任务干扰条件上的差异, 从行为和生理指标探讨认知抑制与创造性思维的关系, 以及时间压力对认知抑制与创造性思维关系的调节作用。实验1采用Stroop颜色命名任务。结果发现, 相比低创者, 高创者的反应时干扰效应量和正确率干扰效应量均更小。实验2采用更灵活的Stroop字义-颜色命名转换任务, 操纵不同的时间压力条件, 并记录被试完成任务时的皮肤电活动。结果发现, 高创者在有时间压力条件下的干扰效应量显著小于无时间压力条件下, 而低创者在有和无时间压力条件下的干扰效应量无显著差异; 高创者在颜色命名任务的不一致条件下的皮肤电活动变化显著高于一致条件, 而低创者在颜色命名任务的一致和不一致条件下无显著差异。研究表明：总体而言, 相比低创者, 高创者的认知抑制能力更高, 能够有效抑制优势的但不相关的反应倾向。时间压力在认知抑制与创造性思维的关系中起调节作用, 高创者面对不同任务要求能够灵活调整自身的认知抑制水平, 并表现出变化的生理唤醒水平。结果支持创造性思维的适应性认知抑制假说。     

高低幸福感人群的负情绪特点：生理和表情的依据

为了检测高、低幸福感人群的负情绪反应诸多特点, 研究在实验室诱发厌恶情绪, 以比较高、低幸福组在情绪主观报告、生理、表情、恢复力及调节策略等方面的差异。组间比较结果显示：(1)负情绪情境下, 低幸福组生理唤醒(HR和GSR)较强, 有较多表情抑制; 高幸福组有更多表情行为, 恢复较快; (2)高幸福组有较强的认知再评习惯。研究提示, 逆境中, 高幸福感人群将有较强的情绪表达与恢复力, 低幸福感人群则保留较强的情绪生理动力。     

Bayesian estimation of item response curves

Item response curves for a set of binary responses are studied from a Bayesian viewpoint of estimating the item parameters. For the two-parameter logistic model with normally distributed ability, restricted bivariate beta priors are used to illustrate the computation of the posterior mode via the EM algorithm. The procedure is illustrated by data from a mathematics test.This work was supported under Contract No. N00014-85-K-0113, NR 150-535, from Personnel and Training Research Programs, Psychological Sciences Division, Office of Naval Research. The authors wish to thank Mark D. Reckase for providing the ACT data used in the illustration and Michael J. Soltys for computational assistance. They also wish to thank the editor and four anonymous reviewers for many valuable suggestions.     

Coding responses and the generalization of matching to sample in children.

Two experiments studied the conditions of stimulus control necessary for the generalization of relational matching to sample. Matching required the selection of comparison shapes rotated 90 degrees clockwise from the orientation of the corresponding sample. In Experiment 1, five children were taught to: (a) code the orientations of samples, (b) transform sample codings to account for the 90 degree rotation, and (c) repeat the transformed sample coding response to a comparison. High levels of generalization occurred with a set of novel stimuli for which stable sample-coding responses were initially available. In another novel set, where stable sample-coding responses were not initially available, low levels of generalized matching were recorded. Matching performance improved after stable coding responses were trained. In Experiment 2, two children and three adults were trained in a form of the matching task that produced poor generalization despite the presence of stable sample-coding responses. Retraining to modify the stimulus control exerted by these coding responses produced an immediate improvement in generalized matching to sample. Results suggest that the generalization of matching is dependent on structure of stimulus control that the component responses exert on each other.     

Cerebral asymmetry in autonomic conditioning to facial expressions: Sex differences

In the present experiment, sex differences in hemispheric asymmetry during classical conditioning to emotional stimuli are reported. 125 subjects (62 females and 63 males) were shown a slide of a happy face in the right (or left) visual half field (VHF), and simultaneously a slide of an angry face in the left (or right) VHF. Eight groups were formed by the combination of male and female subjects; left and right VHF positions of the angry/happy faces; and the administration/omission of the shock unconditioned stimulus (UCS). Dependent measures were skin conductance responses recorded from both hands. The results during extinction showed a significant larger SCR magnitude to the shock compared to the no-shock groups only for the female subjects. CS position during conditioning was also important in revealing differential responding to either the happy or angry faces. A right hemisphere effect was found for the angry face CS for both the male and female subjects, however with a greater difference for the females.     

On conditioned reinforcing effects of negative discriminative stimuli

Observing responses by pigeons were studied during sessions in which a food key and an observing key were available continuously. A variable-interval schedule and extinction alternated randomly on the food key. In one condition, food-key pecking during extinction decreased reinforcement frequency during the next variable-interval component, and in the other condition such pecking did not affect reinforcement frequency. Observing responses either changed both keylight colors from white to green (S+) or to red (S−) depending on the condition on the food key, or the observing responses never produced the S+ but produced the S− when extinction was in effect on the food key. Observing responses that produced only S− were maintained only when food-key pecking during extinction decreased reinforcement frequency in the subsequent variable-interval component. The red light conformed to conventional definitions of a negative discriminative stimulus, rendering results counter to previous findings that production of S− alone does not maintain observing. Rather than offering support for an informational account of conditioned reinforcement, the results are discussed in terms of a molar analysis to account for how stimuli acquire response-maintaining properties.     

The Simon Effect With Wheel-Rotation Responses

The authors examined clockwise and counterclockwise wheel-rotation responses to high- or low-pitched tones presented in participants' (N = 96, Experiment 1; N = 48, Experiment 2; N = 48, Experiment 3) left and right ears. In Experiment 1, a Simon effect (fastest responding when tone location and direction of wheel turn corresponded) was obtained when participants' hands were at the top or middle of the wheel but not at the bottom. With line bottom hand placement, a Simon effect was induced by instructions emphasizing hand movements but not by instructions emphasizing wheel movements (Experiment 2), and by a visual cursor controlled by the wheel but not one triggered by the response (Experiment 3). The results of the experiments showed that the nature of the task and the instructed action goal influence the direction of the Simon effect.