The measurement of time is central to intelligent behavior.

To do so, we extend to neural activity the maximum occupancy principle (MOP) developed for behavior, and refer to this new neural principle asNeuroMOP.NeuroMOP posits thatthegoal ofthenervoussystem istomaximize future action-state entropy, a reward-free, intrinsic motivation that entails creating allpossible activity patterns while avoiding terminal ordangerous ones.

Sparse sequences of neural spikes are posited to underlie aspects of working memory[1],motorproduction[2],andlearning[3,4].

Determining how much of the sensory information carried by a neural code contributes to behavioral performance is key to understand sensory function and neural information flow. However, there are as yet no analytical tools to compute this information that lies at the intersection between sensory coding and behavioral readout.

Brain-computer interfaces (BCIs) often suffer from limited robustness and poor long-term adaptability. Model performance rapidly degrades when user attention fluctuates, brain states shift over time, or irregular artifacts appear during interaction. To mitigate these issues, we introduce a user state-aware electroencephalogram (EEG) filtering framework that refines neural representations before decoding user intentions. The proposed method continuously estimates the user's cognitive state (e.g., focus or distraction) from EEG features and filters unreliable segments by applying adaptive weighting based on the estimated attention level. This filtering stage suppresses noisy or out-of-focus epochs, thereby reducing distributional drift and improving the consistency of subsequent decoding. Experiments on multiple EEG datasets that emulate real BCI scenarios demonstrate that the proposed state-aware filtering enhances classification accuracy and stability across different user states and sessions compared with conventional preprocessing pipelines. These findings highlight that leveraging brain-derived state information--even without additional user labels--can substantially improve the reliability of practical EEG-based BCIs.

Abstract--Objective: The vision-based grasping brain network integrates visual perception with cognitive and motor processes for visuomotor tasks. While invasive recordings have successfully decoded localized neural activity related to grasp type planning and execution, macroscopic neural activation patterns captured by noninvasive electroencephalography (EEG) remain far less understood. Methods: We introduce a novel vision-based grasping platform to investigate grasp-type-specific (precision, power, no-grasp) neural activity across large-scale brain networks using EEG neuroimaging. The platform isolates grasp-specific planning from its associated execution phases in naturalistic visuomotor tasks, where the Filter-Bank Common Spatial Pattern (FBCSP) technique was designed to extract discriminative frequency-specific features within each phase. Support vector machine (SVM) classification discriminated binary (precision vs. power, grasp vs. no-grasp) and multiclass (precision vs. power vs. no-grasp) scenarios for each phase, and were compared against traditional Movement-Related Cortical Potential (MRCP) methods. Results: Low-frequency oscillations (0.5-8 Hz) carry grasp-related information established during planning and maintained throughout execution, with consistent classification performance across both phases (75.3-77.8%) Higher-frequency activity (12-40 Hz) showed phase-dependent results with 93.3% accuracy for grasp vs. no-grasp classification but 61.2% for precision vs. power discrimination. Feature importance using SVM coefficients identified discriminative features within frontoparietal networks during planning and motor networks during execution. Conclusion: This work demonstrated the role of low-frequency oscillations in decoding grasp type during planning using noninvasive EEG. Significance: These findings provide a foundation toward scalable, intention-driven Brain-Machine-Interface (BMI) control strategies.