Author
Listed:
- Rongqi Lin
(South China Normal University, Ministry of Education
South China Normal University
South China Normal University
South China Normal University)
- Xianghong Meng
(Shenzhen University General Hospital)
- Fuyong Chen
(University of Hongkong Shenzhen Hospital)
- Xinyu Li
(Zhejiang Normal University)
- Ole Jensen
(University of Birmingham)
- Jan Theeuwes
(Vrije Universiteit Amsterdam)
- Benchi Wang
(South China Normal University, Ministry of Education
South China Normal University
South China Normal University
South China Normal University)
Abstract
Salient objects often capture our attention, serving as distractors and hindering our current goals. It remains unclear when and how salient distractors interact with our goals, and our knowledge on the neural mechanisms responsible for attentional capture is limited to a few brain regions recorded from non-human primates. Here we conducted a multivariate analysis on human intracranial signals covering most brain regions and successfully dissociated distractor-specific representations from target-arousal signals in the high-frequency (60–100 Hz) activity. We found that salient distractors were processed rapidly around 220 ms, while target-tuning attention was attenuated simultaneously, supporting initial capture by distractors. Notably, neuronal activity specific to the distractor representation was strongest in the superior and middle temporal gyrus, amygdala and anterior cingulate cortex, while there were smaller contributions from the parietal and frontal cortices. These results provide neural evidence for attentional capture by salient distractors engaging a much larger network than previously appreciated.
Suggested Citation
Rongqi Lin & Xianghong Meng & Fuyong Chen & Xinyu Li & Ole Jensen & Jan Theeuwes & Benchi Wang, 2024.
"Neural evidence for attentional capture by salient distractors,"
Nature Human Behaviour, Nature, vol. 8(5), pages 932-944, May.
Handle:
RePEc:nat:nathum:v:8:y:2024:i:5:d:10.1038_s41562-024-01852-5
DOI: 10.1038/s41562-024-01852-5
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