Alpha oscillations shape sensory representation and perceptual sensitivity

Abstract Alpha activity (8–14 Hz) is the dominant rhythm in the awake brain, and thought to play an important role in setting the brain’s internal state. Previous work has associated states of decreased alpha power with enhanced neural excitability. However, evidence is mixed on whether and how such excitability enhancement modulates sensory signals of interest versus noise differently, and what, if any, the consequences are for subsequent perception. Here, human subjects (male and female) performed a visual detection task in which we manipulated their decision criteria in a block-wise manner. While our manipulation led to substantial criterion shifts, these shifts were not reflected in pre-stimulus alpha-band changes. Rather, lower pre-stimulus alpha power in occipital-parietal areas improved perceptual sensitivity and enhanced information content decodable from neural activity patterns. Additionally, oscillatory alpha phase immediately before stimulus presentation modulated accuracy. Together, our results suggest that alpha-band dynamics modulate sensory signals of interest more strongly than noise. Significance statement The internal state of our brain fluctuates, giving rise to variability in perception and action. Neural oscillations, most prominently in the alpha-band, have been suggested to play a role in setting this internal state. Here, we show that ongoing alpha-band activity in occipital-parietal regions predicts the quality of visual information decodable in neural activity patterns, and subsequently human observer’s sensitivity in a visual detection task. Our results provide comprehensive evidence that visual representation is modulated by ongoing alpha-band activity, and advance our understanding on how, when faced with unchanging external stimuli, internal neural fluctuations influence perception and behavior.