Recordings of epidural field potentials (EFPs) allow to acquire neuronal activity over a large region of cortical tissue with minimal invasiveness. Because electrodes are placed on top of the dura and do not enter the neuronal tissue, EFPs offer intriguing options for both clinical and basic science research. On the other hand, EFPs represent the integrated activity of larger neuronal populations, possess a higher trial-by-trial variability, and a reduced signal-to-noise ratio due the additional barrier of the dura. It is thus unclear whether and to what extent EFPs have sufficient spatial selectivity to allow for conclusions about the underlying functional cortical architecture, and whether single EFP trials provide enough information on the short time scales relevant for many clinical and basic neuroscience purposes. We here use the high spatial resolution of primary visual cortex to address these issues and investigate the extent to which very short EFP traces
SignificanceEpidural field potential (EFP) recordings provide a minimally invasive approach to investigate large-scale neural networks and offer intriguing options for basic research and clinical applications. In contrast to subdural recordings, however, the additional barrier of the dura potentially enlarges the neuronal population over which activity is integrated, and decreases both signal-to-noise ratio and spatial resolution. Here we show that despite these constrains singletrial EFPs constitute a highly reliable, selective, and clearly localized source of information. By making use of the spatial selectivity of primary visual cortex, we show that single trial information can be decoded with close-to-perfect performance, even without using advanced classifiers and based on very few data. This labels EFPs as a highly attractive and widely usable signal.