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In the early 1980s, Libet found that a readiness potential (RP) over central scalp locations begins on average several hundred milliseconds before the reported time of awareness of willing to move (W). Haggard and Eimer Exp Brain Res 126(1):128-133, (1999) later found no correlation between the timing of the RP and W, suggesting that the RP does not reflect processes causal of W. However, they did find a positive correlation between the onset of the lateralized readiness potential (LRP) and W, suggesting that the LRP might reflect processes causal of W. Here, we report a failure to replicate Haggard and Eimer's LRP finding with a larger group of participants and several variations of their analytical method. Although we did find a between-subject correlation in just one of 12 related analyses of the LRP, we crucially found no within-subject covariation between LRP onset and W. These results suggest that the RP and LRP reflect processes independent of will and consciousness. This conclusion has significant implications for our understanding of the neural basis of motor action and potentially for arguments about free will and the causal role of consciousness.

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Retinal signals are transmitted to cortex via neurons in the lateral geniculate nucleus (LGN), where they are processed in burst or tonic response mode. Burst mode occurs when LGN neurons are sufficiently hyperpolarized for T-type Ca 2ϩ channels to deinactivate, allowing them to open in response to depolarization, which can trigger a high-frequency sequence of Na ϩ-based spikes (i.e., burst). In contrast, T-type channels are inactivated during tonic mode and do not contribute to spiking. Although burst mode is commonly associated with sleep and the disruption of retinogeniculate communication, bursts can also be triggered by visual stimulation, thereby transforming the retinal signals relayed to the cortex. To determine how burst mode affects retinogeniculate communication, we made recordings from monosynaptically connected retinal ganglion cells and LGN neurons in male/female cats during visual stimulation. Our results reveal a robust augmentation of retinal signals within the LGN during burst mode. Specifically, retinal spikes were more effective and often triggered multiple LGN spikes during periods likely to have increased T-type Ca 2ϩ channel activity. Consistent with the biophysical properties of T-type Ca 2ϩ channels, analysis revealed that effect magnitude was correlated with the duration of the preceding thalamic interspike interval and occurred even in the absence of classically defined bursts. Importantly, the augmentation of geniculate responses to retinal input was not associated with a degradation of visual signals. Together, these results indicate a graded nature of response mode and suggest that, under certain conditions, bursts facilitate the transmission of visual information to the cortex by amplifying retinal signals.

Significance We do not know how the human brain mediates complex and creative behaviors such as artistic, scientific, and mathematical thought. Scholars theorize that these abilities require conscious experience as realized in a widespread neural network, or “mental workspace,” that represents and manipulates images, symbols, and other mental constructs across a variety of domains. Evidence for such a complex, interconnected network has been difficult to produce with current techniques that mainly study brain activity in isolation and are insensitive to distributed informational processes. The present work takes advantage of emerging techniques in network and information analysis to provide empirical support for such a widespread and interconnected information processing network in the brain that supports the manipulation of visual imagery.