Reaching Movement Onset- and End-Related Characteristics of EEG Spectral Power Modulations

The spectral power of intracranial field potentials shows movement-related modulations during reaching movements to different target positions that in frequencies up to the high-γ range (approximately 50 to above 200 Hz) can be reliably used for single-trial inference of movement parameters. However, identifying spectral power modulations suitable for single-trial analysis for non-invasive approaches remains a challenge. We recorded non-invasive electroencephalography (EEG) during a self-paced center-out and center-in arm movement task, resulting in eight reaching movement classes (four center-out, four center-in). We found distinct slow (≤5 Hz), μ (7.5–10 Hz), β (12.5–25 Hz), low-γ (approximately 27.5–50 Hz), and high-γ (above 50 Hz) movement onset- and end-related responses. Movement class-specific spectral power modulations were restricted to the β band at approximately 1 s after movement end and could be explained by the sensitivity of this response to different static, post-movement electromyography (EMG) levels. Based on the β band, significant single-trial inference of reaching movement endpoints was possible. The findings of the present study support the idea that single-trial decoding of different reaching movements from non-invasive EEG spectral power modulations is possible, but also suggest that the informative time window is after movement end and that the informative frequency range is restricted to the β band

The role of ECoG magnitude and phase in decoding position, velocity and acceleration during continuous motor behavior

In neuronal population signals, including the electroencephalogram (EEG) and electrocorticogram (ECoG), the low-frequency component (LFC) is particularly informative about motor behavior and can be used for decoding movement parameters for brain-machine interface (BMI) applications. An idea previously expressed, but as of yet not quantitatively tested, is that it is the LFC phase that is the main source of decodable information. To test this issue, we analyzed human ECoG recorded during a game-like, one-dimensional, continuous motor task with a novel decoding method suitable for unfolding magnitude and phase explicitly into a complex-valued, time-frequency signal representation, enabling quantification of the decodable information within the temporal, spatial and frequency domains and allowing disambiguation of the phase contribution from that of the spectral magnitude. The decoding accuracy based only on phase information was substantially (at least 2 fold) and significantly higher than that based only on magnitudes for position, velocity and acceleration. The frequency profile of movement-related information in the ECoG data matched well with the frequency profile expected when assuming a close time-domain correlate of movement velocity in the ECoG, e.g., a (noisy) copy of hand velocity. No such match was observed with the frequency profiles expected when assuming a copy of either hand position or acceleration. There was also no indication of additional magnitude-based mechanisms encoding movement information in the LFC range. Thus, our study contributes to elucidating the nature of the informative low-frequency component of motor cortical population activity and may hence contribute to improve decoding strategies and BMI performance

Neural system prediction and identification challenge

Can we infer the function of a biological neural network (BNN) if we know the connectivity and activity of all its constituent neurons? This question is at the core of neuroscience and, accordingly, various methods have been developed to record the activity and connectivity of as many neurons as possible. Surprisingly, there is no theoretical or computational demonstration that neuronal activity and connectivity are indeed sufficient to infer the function of a BNN. Therefore, we pose the Neural Systems Identification and Prediction Challenge (nuSPIC). We provide the connectivity and activity of all neurons and invite participants (1) to infer the functions implemented (hard-wired) in spiking neural networks (SNNs) by stimulating and recording the activity of neurons and, (2) to implement predefined mathematical/biological functions using SNNs. The nuSPICs can be accessed via a web-interface to the NEST simulator and the user is not required to know any specific programming language. Furthermore, the nuSPICs can be used as a teaching tool. Finally, nuSPICs use the crowd-sourcing model to address scientific issues. With this computational approach we aim to identify which functions can be inferred by systematic recordings of neuronal activity and connectivity. In addition, nuSPICs will help the design and application of new experimental paradigms based on the structure of the SNN and the presumed function which is to be discovered

Push-pull receptive field organization and synaptic depression: Mechanisms for reliably encoding naturalistic stimuli in V1

Neurons in the primary visual cortex are known for responding vigorously but with high variability to classical stimuli such as drifting bars or gratings. By contrast, natural scenes are encoded more efficiently by sparse and temporal precise spiking responses. We used a conductance-based model of the visual system in higher mammals to investigate how two specific features of the thalamo-cortical pathway, namely push-pull receptive field organization and synaptic depression, can contribute to this contextual reshaping of V1 responses. By comparing cortical dynamics evoked respectively by natural vs. artificial stimuli in a comprehensive parametric space analysis, we demonstrate that the reliability and sparseness of the spiking responses during natural vision is not a mere consequence of the increased bandwidth in the sensory input spectrum. Rather, it results from the combined impacts of synaptic depression and push-pull inhibition, the later acting for natural scenes as a form of effective feed-forward inhibition as demonstrated in other sensory systems. Thus, the combination of feedforward-like inhibition with fast thalamo-cortical synaptic depression by simple cells receiving a direct structured input from thalamus composes a generic computational mechanism for generating a sparse and reliable encoding of natural sensory events