The driver’s attentional state is a significant human factor in traffic safety. The executive control process is a crucial sub−function of attention. To explore the relationship between the driver’s driving performance and executive control function, a total of 35 healthy subjects were invited to take part in a simulated driving experiment and a task−cuing experiment. The subjects were divided into three groups according to their driving performance (aberrant driving behaviors, including lapses and errors) by the clustering method. Then the performance efficiency and electroencephalogram (EEG) data acquired in the task−cuing experiment were compared among the three groups. The effect of group, task transition types and cue−stimulus intervals (CSIs) were statistically analyzed by using the repeated measures analysis of variance (ANOVA) and the post hoc simple effect analysis. The subjects with lower driving error rates had better executive control efficiency as indicated by the reaction time (RT) and error rate in the task−cuing experiment, which was related with their better capability to allocate the available attentional resources, to express the external stimuli and to process the information in the nervous system, especially the fronto−parietal network. The activation degree of the frontal area fluctuated, and of the parietal area gradually increased along with the increase of CSI, which implied the role of the frontal area in task setting reconstruction and working memory maintaining, and of the parietal area in stimulus−response (S−R) mapping expression. This research presented evidence of the close relationship between executive control functions and driving performance.

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Lactoalbumin hydrolysate (LH) at 100 mg L -1 with methyl jasmonate (MJ) at 2 mg L -1 synergistically stimulated ginsenoside accumulation in Panax quinquefolium cells compared with 100 mg L -1 LH. Combination elicitors led to higher ginsenoside productivity (45.93 mg L -1 ) than single treatment of 100 mg L -1 LH (31.37 mg L -1 ). This present result will be helpful in providing a tool for enhancing the productivity of ginsenoside by Panax quinquefolium cell cultures on a commercial scale.