Spatiotemporal evidence uncovers differential neural activity patterns in cognitive and affective conflict control.

Studies have shown that there are overlapping neural bases for cognitive and affective conflict control, but whether the neural activity patterns caused by the two types of conflict are similar remains to be explored. The present study utilizes electroencephalogram (EEG) and functional magnetic resonance imaging (fMRI) to temporally and spatially analyze the differences between cognitive and affective conflict control. We employ a semantic conflict task which includes blocks of cognitive and affective judgements primed by conflicting and non-conflicting contexts. The results showed a typical neural conflict effect in the cognitive judgment blocks as reflected by greater amplitudes of P2, N400, and the late positive potential (LPP), as well as greater activation of the left pre-supplementary motor area (pre-SMA) and the right inferior frontal gyrus (IFG) in the conflict condition relative to the non-conflict condition. These patterns did not emerge in the affective judgments, but instead, showed reversed effects of the LPP and in the left SMA. Taken together, these findings suggest that cognitive and affective conflict control result in different neural activity patterns.

Genetic bases of language control in bilinguals: Evidence from an EEG study.

Previous studies have debated whether the ability for bilinguals to mentally control their languages is a consequence of their experiences switching between languages or whether it is a specific, yet highly-adaptive, cognitive ability. The current study investigates how variations in the language-related gene FOXP2 and executive function-related genes COMT, BDNF, and Kibra/WWC1 affect bilingual language control during two phases of speech production, namely the language schema phase (i.e., the selection of one language or another) and lexical response phase (i.e., utterance of the target). Chinese-English bilinguals (N = 119) participated in a picture-naming task involving cued language switches. Statistical analyses showed that both genes significantly influenced language control on neural coding and behavioral performance. Specifically, FOXP2 rs1456031 showed a wide-ranging effect on language control, including RTs, F(2, 113) = 4.00, FDR p = .036, and neural coding across three-time phases (N2a: F(2, 113) = 4.96, FDR p = .014; N2b: F(2, 113) = 4.30, FDR p = .028, LPC: F(2, 113) = 2.82, FDR p = .060), while the COMT rs4818 (ts >2.69, FDR ps < .05), BDNF rs6265 (Fs >5.31, FDR ps < .05), and Kibra/WWC1 rs17070145 (ts > -3.29, FDR ps < .05) polymorphisms influenced two-time phases (N2a and N2b). Time-resolved correlation analyses revealed that the relationship between neural coding and cognitive performance is modulated by genetic variations in all four genes. In all, these findings suggest that bilingual language control is shaped by an individual's experience switching between languages and their inherent genome.