Neuroscience of Consciousness

Effortful cognition is typically associated with controlled, task-constrained neural processing, whereas effortless awareness may require a more flexible, internally driven mode of brain organization. Critical brain dynamics provide a principled framework for characterizing this shift, as systems near criticality are thought to balance stability and flexibility, allowing efficient information processing without excessive control. Transcendental Meditation (TM), characterized by a shift from effortful mental engagement to effortless awareness, offers a natural model for testing this possibility. Here, we investigated whether critical brain dynamics track TM as a global meditative state, or instead reflect moment-to-moment fluctuations in subjective effortlessness. We combined high-density electroencephalography (EEG) with time-resolved phenomenological reports using Temporal Experience Tracing (TET). Experienced TM practitioners (N = 33) and matched controls (N = 33) completed resting-state recordings before and after a 30-minute TM or silent counting control task. Long-range temporal correlations (LRTCs) were quantified using detrended fluctuation analysis, while functional excitation/inhibition (fEI) balance was used to estimate directional deviations from criticality. State-based analyses showed that TM increased alpha and beta LRTCs relative to pre- and post-resting state within meditators, but revealed no robust between-group differences in either LRTCs or fEI balance. In contrast, neurophenomenological analyses showed that subjective effortlessness was robustly associated with increased theta, alpha, beta, and broadband LRTCs, with significantly stronger relationships in meditators than controls. Restricting analyses to low-effort periods further revealed higher beta LRTCs in meditators, a difference missed by conventional state comparisons. These findings identify scale-free neural dynamics as a candidate marker of "letting go" during meditation.

Why does an angry face feel uncomfortable? The answer is that it signals a threat. However, a face is only part of an encounter, and distance, facial stimulus type, and gaze may shape discomfort regardless of perceived anger. To separate these cues, we conducted three within-subjects virtual reality experiments. In each experiment, 24 adults viewed avatars at intimate, personal, and social distances (30, 100, and 300 cm, respectively) and rated the faces perceived anger and their own discomfort; head movement was recorded in Experiments 2 and 3. In Experiment 1, the expression (angry, neutral) and facial color (natural, red) were crossed with distance; in Experiment 2, a featureless mannequin served as a nonface comparison; and in Experiment 3, the gaze direction (direct, averted) was manipulated. Expression primarily determined perceived anger, whereas distance predominantly determined discomfort: A nearby neutral face was uncomfortable despite low perceived anger (Experiment 1). A neutral human face was more uncomfortable than a mannequin, although both received similarly low perceived-anger ratings (Experiment 2). Direct gaze increased the discomfort without changing perceived anger (Experiment 3). Backward head movement exhibited a similar pattern, with participants leaning back more from human faces than from the mannequin. These results indicate that the discomfort associated with an angry face is not merely explained by perceived anger. Instead, social discomfort was differentially associated with interpersonal distance and gaze direction and differed between the human-face and mannequin conditions.

During wakefulness, we are used to perceive the environment through our senses, act on it and take these inputs to update our experiences and build the perceptions. When the inputs are not longer accurate or structured, people would sometimes have hallucinatory experiences. Whether such experiences are associated with distinct patterns of thought, and how they relate to large scale brain dynamics, remains unclear. To address these questions, we combined experience sampling protocol with EEG recording during multimodal Ganzfeld, where participants were exposed to unstructured, uniform visual and auditory stimulation. Participants repeatedly reported the complexity of their visual experiences together with ongoing thoughts related to perceptual belief, prediction perception mismatch, active updating, and prior mentation. EEG microstates were extracted to characterize the temporal dynamics of large-scale brain networks. We found that visual complexity was related to all four dimensions, but partly distinct in simple and complex visual experiences. These phenomenological changes were accompanied by distinct, and often nonlinear, dynamics of large-scale brain networks involved in visual processing, salience detection, and internally directed cognition. It also indicates that this paradigm might be a valuable model for investigating the mechanisms underlying hallucinatory experiences in psychosis.

Museum visits typically follow curator-defined routes that constrain how visitors shape their own experience, yet choice is widely held to heighten engagement, autonomy, and enjoyment. Virtual reality (VR) offers a setting in which to study these processes because it combines ecological immersion with precise, continuous behavioral measurement. We investigated (i) whether VR- derived behavioral signals are associated with self-reported enjoyment during a virtual museum tour, and (ii) whether the level of agency afforded to visitors influences enjoyment. Forty-eight adults completed a room-scale, life-size VR tour (8 * 4 m) of seven paintings from the Tel Aviv Museum of Art, each accompanied by a synchronized audio guide. Synchronized gaze and head- position streams were logged continuously (50 Hz) and segmented into painting-level viewing episodes using a trial-and-tile pipeline that intersects each painting's trial interval with an empirically defined spatial window in front of the canvas. Participants were randomly assigned to one of three agency conditions, Active (choice before every artwork), Semi-Active (choice for the first three), or Passive (fixed route),while the artwork sequence was held identical. Self- reported enjoyment at the tour and painting levels did not differ reliably across agency conditions. Among VR-derived measures, gaze engagement during the audio guide showed the clearest (though modest) association with painting-level liking, whereas locomotion and pacing measures were weak and inconsistent predictors. Agency nonetheless reliably modulated several gaze- and time-based viewing measures. The findings reveal a dissociation between subjective enjoyment and the micro-structure of viewing, and establish a reusable framework for full-tour, painting-level behavioral analysis in immersive settings.

Identifying neural signatures of consciousness remains a central challenge in neuroscience. Sleep offers a tractable model for comparing brain activity in the presence or absence of subjective experience while minimizing behavioral responsiveness confounds. Using overnight 256 electrode high-density EEG in 140 participants and a serial-awakening paradigm, we analyzed 699 non-rapid eye movement (NREM) sleep stage 2 and 3 awakenings (351 dreaming experience, 348 no experience). Features from the 60s preceding awakening included regional spectral power, lagged-coherence connectivity, graph-theoretic metrics and gamma-to-alpha power ratios. Dreaming experiences were associated with shifts in posterior spectral balance, particularly reduced alpha and delta power and increased gamma-related measures, together with altered large scale network organization. In participant-level cross-validated machine-learning analyses, all classifiers performed above chance, with the best ensemble model reaching an ROC-AUC of 0.80 and average precision of 0.80. These findings identify reproducible posterior electrophysiological and network-level signatures of conscious states during NREM sleep.

Sleep spindles, transient 11-16 Hz oscillatory bursts, are a defining electrographic feature of non-rem (NREM) sleep and a key biomarker of sleep physiology. A need for efficient and reliable identification of spindles motivates a large literature on automated detection algorithms. In this literature, annotation by trained sleep specialists remains the gold standard against which automated methods are trained, tuned and evaluated. However, inter-scorer agreement among experts is modest, which leaves a significant role for subjective judgment in the definition of a spindle. Finding objective, scorer-independent, criteria for identifying spindles remains an unresolved challenge. We report here a robust, highly specific, and previously unrecognized signature of spindle activity in the fourth-order spectrum (trispectrum), from which we identify the presence of spindles, characterize their waveforms, and obtain an optimal detection filter through a decomposition of the trispectrum (HOSD). Although it is a strictly blind, data-driven method, HOSD-based spindle identification and detection agrees well with expert annotation (median AUROC ~0.9), yet identifies many more events at the native threshold than both human scorers and comparison detectors. Many of these additional detections are confirmed as meeting AASM spindle criteria by four blinded specialists, demonstrating that spindle-like oscillatory bursting is prevalent below conventional human and automated detection thresholds. We observe that N2 sleep is distinguished principally by high-amplitude bursts, while low-amplitude bursting persists throughout NREM sleep, being globally suppressed only in REM sleep. We also describe robust identification of recording-specific spindle waveform properties such as frequency deceleration.

Humans rapidly assess the beauty of natural scene images. Previous EEG work suggests neural representations of beauty emerge early and are temporally sustained. Complementary fMRI work pinpoints the neural correlates of beauty to visual, frontal, and default-mode network areas. An integrated view of the spatiotemporal dynamics that give rise to the perception of beauty, however, is lacking. Beyond the beauty of the depicted scene, the quality of the image itself influences its perceived beauty, and it is unknown how the brain separates these two factors. To address these questions, we recorded EEG (N = 52) and fMRI (N = 29) data while participants rated the beauty of 100 natural scene photographs. Another group of participants (N = 46) rated the image quality of the same photographs. Separate representational similarity analyses on the EEG and fMRI data revealed early and sustained beauty-related representations across widespread cortical areas. In contrast, representations of image quality emerged earlier, had markedly different representational dynamics, and were predominantly localized to visual cortex. In a model-based EEG-fMRI fusion analysis, we investigated how the correspondence between temporally resolved EEG signals and spatially resolved fMRI signals is explained by beauty ratings. Our results suggest that beauty-related representations emerge early (from around 165ms and peaking at 275ms post-onset), are long-lasting, and primarily originate from high-level visual cortex. This spatiotemporal signature persisted when controlling for image-quality ratings. Our findings emphasize the importance of perceptual processing for perceived beauty and suggest that the brain represents aesthetic appeal independently of image quality.

Analysis does not always enhance aesthetic experience. Philosophical accounts have long suggested that decomposing an aesthetic experience into determinate components may weaken it, yet this possibility has rarely been tested experimentally. To examine whether, when, and how analysis produces divergent effects on aesthetic experience, we conducted two experiments manipulating analysis depth. Experiment 1 showed that, during affective analysis of visual art, deep analysis produced a significantly weaker increase in aesthetic ratings than shallow analysis. In Experiment 2, we selected this condition to investigate the underlying mechanism. The behavioral effect was replicated: deep analysis removed the increase produced by shallow analysis without reducing ratings below the image baseline. Frequency-resolved brain network analysis further revealed a stronger task-related component and higher spatial entropy within the default mode network under deep analysis. Network-behavior correlations observed under shallow analysis were absent under deep analysis, suggesting reduced correspondence between the default-mode network (DMN) organization and aesthetic experience. Exploratory analyses further showed that spatial weights in the lateral temporal cortex and inferior parietal lobule were associated with smaller increases in aesthetic ratings. Together, these findings indicate that deeper analysis can selectively weaken improvements in aesthetic experience by altering how affective information is organized within the DMN.

Sleep is critical for memory consolidation and emotional regulation, yet the respective roles of non-rapid eye movement (NREM) and rapid eye movement (REM) sleep remain unclear. Here, using a within-subject crossover design, we recorded high-density electroencephalography (EEG) across two experimental nights while participants viewed neutral or aversive film clips in a counterbalanced order. Combining with daytime functional localizers establishing neural patterns of aversive vs. neutral emotional processing, multivariate pattern analysis revealed that the reactivation of aversive vs. neutral memory during nocturnal sleep was both stage-dependent and event-specific. In NREM sleep, valence-specific reactivation was time-locked to slow oscillation (SO)-spindle complexes but not to either event alone; in REM sleep, reactivation occurred selectively during phasic REM periods marked by rapid eye movements. Critically, NREM SO-spindle coupling percentage was associated with consolidation of temporal memories; whereas phasic REM reactivation strength was linked to overnight dissipation of negative affect. Our findings provide direct evidence that sleep reprocesses emotional experiences through dissociable stage- and event-specific mechanisms, laying out a framework for future targeted sleep-based interventions.

Sleepiness is a leading proximate cause of drowsy-driving fatalities, medical errors and industrial accidents, yet it has resisted mechanistic prediction; although it arises from well-characterized sleep-wake physiology, it is experienced as a subjective state and has lacked a quantitative link to the underlying dynamics. We previously showed that subjective sleepiness maps linearly, with a protocol-invariant form, onto the signed distance H - H+ between the homeostatic pressure H and the circadian-modulated sleep-onset threshold H+. This single quantity predicts sleepiness accurately but is mechanistically ambiguous: the same value can arise either because H sits far from the boundary or because the threshold H+(t) has shifted with circadian phase, and these two origins call for entirely different interpretations and interventions. Here we resolve this ambiguity by decomposing H - H+ into two mechanistically separable axes-intensity and phase. The intensity axis is the time-averaged margin [<] H - H+[>], set by how far, on average, H sits from the sleep boundary: slowed homeostatic accumulation accounts for the paradoxically blunted sleepiness of older adults, and pharmacological suppression of H accounts for the dose-dependent alerting effect of caffeine. The phase axis is set by the circadian modulation of H+(t): under a forced-desynchrony protocol, in which the pacemaker free-runs and the homeostatic and circadian processes are experimentally decoupled, sleepiness tracks the circadian profile of H+(t) across all phases while the intensity mapping itself remains unchanged-a clean dissociation of the two axes. By resolving felt sleepiness into these two physiological degrees of freedom, this framework renders previously isolated phenomena-aging, caffeine and circadian misalignment-commensurable within a single theory and provides a physiologically interpretable basis for prospective fatigue-risk prediction. Author summaryWhy people feel sleepy after sleep loss, or at particular times of day, remains difficult to predict from physiology alone. Sleep and wake are shaped by two interacting processes: a daily circadian rhythm and a homeostatic pressure that builds during wakefulness. In earlier work, we linked subjective sleepiness ratings to a simple geometric quantity-how close sleep pressure sits to a circadian sleep-onset boundary. That link is useful, but ambiguous: the same distance can arise either because pressure itself has changed, or because the boundary has moved with circadian phase. Here we use a computational model of the sleep-wake switch, extended to include the wake-stabilizing orexin system, to separate these contributions into an intensity axis and a phase axis. We find that aging and caffeine mainly alter how large the average distance to the boundary becomes, whereas forced desynchrony mainly alters how that distance varies across circadian phase. This dissociation offers a compact way to interpret several otherwise separate observations within one quantitative picture, and a step toward more physiologically grounded fatigue-risk assessment.

We identified Sleep Bursts (SBs), as a novel phenomenon of brief (1-2 sec), often periodic bursts in cranial forces occurring during human sleep. Our goal was to characterize SBs in normal subjects, then compare SB in a cohort of subjects with neurodegenerative disease (NDD). We recorded 32 cognitively healthy subjects (23 -87 years) and 13 subjects with NDD (51 - 84 years). SBs occurred in all 45 subjects. SBs occurred at 0.57 SB/min (once per 105 seconds) in controls and 0.40 SB/min (once per 150 seconds) in NDD (p = 0.0043). SB occurred with equal rates across all sleep stages in both groups. When occurring periodically, SBs had modal intervals (3.75 bursts/min (0.0625 Hz) - 2.67 bursts/min (0.044 Hz)). EEG power increased in the delta range 1-2 seconds before and following the SB. EEG delta power during a SB was significantly lower in all NDD subjects across sleep stages compared to controls. The relatively low frequency of SB events and synchronization with EEG power has no parallel in human sleep; we hypothesize that SBs may represent a brain-generated pulsatile component of brain glymphatic drainage.

Introduction: Decision making for selecting an object or a course of action from possible alternatives largely depends on our perceptual ability modulated by attention. When multiple stimuli appear close together in time, processing one stimulus can temporarily impair the processing of another due to temporal limitations of attention. Observers frequently fail to detect the second target (T2) presented within a few hundred milliseconds after the first target (T1) in a stream of stimuli, which is commonly known as attentional blink (AB). Existing theories attribute this perceptual lapse to T1 processing, distractor interference, or transient attentional gating; however, the computations underlying suppressive mechanism remains unresolved. We investigated whether pupil-size could reveal the underlying mechanisms of AB and predict conscious perception on a trial-by-trial basis. Methods: Pupil diameter and gaze locations were recorded using an infrared eye tracker. Machine learning techniques were used to classify trials when T2 was detected versus when it was not, after correct identification of T1, during an AB task from the pupil dynamics, which also yielded attentional episode (AE) associated with each element in the stream of visual stimuli when deconvolved. Results: Cross-validating classifiers achieved near-perfect accuracy not only in distinguishing but also predicting perceptual outcomes on a single-trial basis. AEs exhibited greater power when T2 was detected than when it was missed; the differential power in AEs on a logarithmic scale was highly synced with the differential pupil size. Conclusions: Collectively, these findings establish a framework for predicting attention-driven perceptual outcomes from pupil-dynamics at finer time-scale.

Chronic fatigue, characterized by persistent physical and/or mental exhaustion, is a frequent and debilitating symptom in medicine. Despite its impact, clinical management remains a challenge. A key problem is the absence of any biomarkers; as a consequence, diagnosis rests entirely on patients' self-report. This contributes to patient stigmatization and highlights the need for objective diagnostic tools. In this study, we explored the feasibility of constructing computational assays of chronic fatigue, using clinical and functional neuroimaging data from over 2,200 participants in the UK Biobank. Whole-brain analyses of functional and effective connectivity were followed by machine learning, based on a preregistered analysis plan and a strict separation of training data and held-out test data. We found that clinical data, including prior medical diagnoses, cancer history, sleep-related information, and alcohol consumption, enabled a statistically significant prediction of chronic fatigue (61% balanced accuracy, p=0.001). Combining clinical information with brain connectivity data again enabled statistically significant predictions (up to 64% balanced accuracy) but did not consistently outperform the model trained on clinical data only. Across all models, sleep-related information, especially insomnia symptoms, emerged as a particularly important feature for prediction. Our results suggest a high degree of heterogeneity amongst individuals with chronic fatigue. While the predictive performance achieved in this study is not yet sufficient for clinical application, our findings provide a foundation for future developments of objective assays of fatigue. In particular, our results highlight the importance of sleep-related information and suggest new avenues for harnessing neuroimaging information for the prediction of fatigue.

Attention forms a key, yet elusive component of visual processing. We shift attention constantly across the visual field to enhance processing of relevant locations or stimuli in service of goal-directed behavior. Here, we investigate a fundamental property of attentional shifts: when covertly shifting from one location to another, does visual attention "travel" (enhance processing at intermediate locations) or "teleport" (not interact with intermediate locations)? While most shifts of information or movement "travel" (e.g., eye and body movements, neuronal signalling), for attentional shifts such intermediate processing enhancement might not be necessary, nor functional. To answer this question while tackling the difficulty of tracking covert attentional dynamics, we conducted an EEG-eyetracking experiment (n=24) paired with Rapid Invisible Frequency Tagging (RIFT). This let us track attentional enhancement during covert attentional shifts with high temporal and spatial precision. We successfully registered covert shifts, but found no evidence for any attentional modulation in-between the start and end-point of an attentional shift. Additional insilico modelling of attentional shifts confirmed that our method was sensitive enough to pick up on these modulations had they been present. Our results support a "teleporting" model of attention, suggesting that attention is implemented in a fundamentally different manner compared to overt visual behaviours such as eye movements.

Wayfinding in hospitals is often hindered by ineffective signage; however, the cognitive mechanisms of healthcare wayfinding symbols comprehension remain under-researched. This study utilized eye-tracking and spatial gaze mapping to examine how visual complexity, abstraction, and human figuration modulate perception in 40 healthy adults viewing 24 hospital-related healthcare wayfinding symbols. Results indicate that pupil size is a sensitive physiological marker of cognitive load, significantly influenced by visual complexity ({chi}2 = 11.32, p = .022) and abstraction ({chi}2 = 7.49, p = .027). Human figuration reduced fixation duration and increased saccade amplitude, facilitating efficient semantic integration. Furthermore, human-centric healthcare wayfinding symbols elicited streamlined gaze trajectories, whereas abstract/complex designs induced chaotic scanpaths. These findings suggest that human figuration acts as a cognitive scaffold, reducing mental effort. We provide evidence-based guidelines for optimizing healthcare wayfinding symbols by prioritizing human body representations and balancing abstraction levels. HighlightO_LIPupil size indexes cognitive load during symbol comprehension. C_LIO_LIHuman figuration cuts fixation duration, boosting wayfinding efficiency. C_LIO_LIAbstract symbols increase pupil dilation, raising cognitive load. C_LI

The human face is central to social interactions, supporting the ability to interpret others mental states using theory of mind (ToM). We examined whether functional near-infrared spectroscopy (fNIRS) would reveal brain-activation differences between live and pre-recorded social conversations in brain regions implicated in ToM. Furthermore, we examined whether activation depended on the visual realism of a social partner - viewed as a human or an animated avatar. By one view, social interactions may be dependent on how natural the social partner appears; by another view, social interactions may depend only upon the attribution of responses to a real human regardless of visual appearance. Neural activation for pre-recorded compared to live interactions was prolonged, consistent with extended cognitive effort. Activation patterns in the right temporoparietal junction differed between interacting with humans versus avatars, along with a stronger preference for looking at the eyes when interacting with a human (vs. avatar), underscoring the social relevance of real faces. Findings highlight the importance of both live interactions and facial realism in shaping social-cognitive processing, a finding with relevance for optimizing online social interactions.

Recognizing others emotions is central to social interaction. Traditional biological psychology infers emotional responding via laboratory measures, whereas contemporary computer vision algorithms claim to identify emotions unobtrusively from facial video. However, the validity of such algorithms for classifying spontaneous emotional responses occurring without explicit communicative intent remains debated. We compared established psychophysiological measures (EEG, facial EMG, EDA activity) with the open-source facial behavior toolkit OpenFace for classifying participants spontaneous responses during free viewing of happiness-inducing, disgust-inducing, and neutral pictures. Participants provided valence and arousal ratings and later selected the basic emotion that best matched their reaction which served as the classification criterion. Using within-participants single-trial support vector machine (SVM) classification, EEG achieved the highest accuracy (40%), followed by facial EMG (37%); OpenFace reached 36%. All methods except EDA exceeded chance performance (33.3%) and were lower compared to human raters (48%). Predictions declined slightly for across-participants SVMs, being at chance for OpenFace and EDA. The results indicate that in principle both, psychophysiological measures and video-derived facial action units, can capture diagnostically relevant aspects of emotional responding during picture viewing, but that their performance is limited when expressions are spontaneous and not produced for communicative purposes. Inter-individual variability in expressivity and physiological responding likely contributes to these limitations and should be considered when deploying automatic emotion recognition in research or applied settings.

Tactile imagery has attracted growing fundamental and clinical interest. Previous studies often investigated neural and functional similarities between imagined and actual touch. Several functional aspects of touch, such as differences between active and passive touch, between different haptic features during active touch or sensitivity of different body parts for passive touch, have also been explored in tactile imagery. Furthermore, considerable individual differences in the ability to engage in tactile imagery have been observed. However, several important aspects, involving different imagery components and a wide variety of touch qualities remain to be explored within a single comprehensive study. The current study therefore aims to provide a wide-ranging assessment of tactile imagery in terms of imagery processing components (vividness, maintenance, transformation), type of touch (active versus passive) and touch qualities (object properties for active touch, different tactile sensations across body sites for passive touch). We developed a comprehensive questionnaire containing 72 items to assess tactile imagery ability. 136 healthy participants were asked to imagine different touch types and rate imagery vividness and their ability to maintain and transform each sensation on 5-point Likert-scales. Active touch varied by object (plastic bottle, modeling clay, sponge) and property (temperature, weight, texture, resistance). Passive touch varied by body site (lip, shin, sole of the foot, lower back) and sensation (stroking, vibration, pinching). Overall, participants were able to perform tactile imagery: the vast majority reported at least some imagery across touch types. Individual variability was substantial: scores bridged both ends of the scale. Active tactile imagery differed significantly between objects, depending on tactile property. Object-property pairs with particularly strong imagery were bottle-temperature, bottle-weight and sponge-texture, whereas bottle-resistance elicited weaker imagery, as did temperature and weight for both sponge and clay. Passive tactile imagery was significantly stronger for body sites with higher receptor density (i.e. lip and foot). Imagery of stroking was significantly weaker than vibration and pinching. Active and passive imagery showed a strong, positive correlation, though some participants had relatively strong active imagery, but weaker passive imagery, or vice versa. Our findings confirm that tactile imagery ability varies across individuals and touch types, underlining the importance of a comprehensive imagery ability assessment tool specific to the tactile domain.

Music perception and musical imagery provide a controlled setting for studying whether scalp electroencephalography (EEG) captures reproducible differences between externally driven and internally generated auditory states. We tested whether the public OpenMIIR dataset supports leakage-aware decoding of music perception versus cued musical imagery across its full ten-subject cohort, and we characterized the boundary beyond which the decoded signal fails to generalize. Using compact spectral and temporal EEG features, we applied stratified trial-grouped cross-validation, dummy and shuffled-label negative controls, leave-one-subject-out (LOSO) testing, a 1000-fold trial-level label-permutation test, and a group-level one-sided Wilcoxon test over per-subject within-subject accuracies, with Benjamini-Hochberg (BH) correction across the family of tested hypotheses. Within subjects, decoding was above chance at the population level: a group Wilcoxon test on logistic-regression accuracy gave p = 0.0195 with a large effect size (Cohens dz = 0.95; 7 of 10 subjects above chance), confirmed by a pooled trial-level permutation test (p = 0.0040). Pooled trial-grouped balanced accuracy reached 0.567 [0.550,0.586] for random forest and 0.543 [0.523,0.561] for logistic regression, exceeding both dummy and shuffled-label controls. Cross-subject transfer was weaker and model-dependent: under LOSO, random forest reached 0.559 [0.523, 0.597], above its dummy baseline (uncorrected p = 0.014), whereas logistic regression did not generalize (0.518, p = 0.165). Under BH correction across the nine tested hypotheses, six comparisons survived at q < 0.05 (smallest q = 0.036), all involving the permutation test or the nonlinear model, while the linear models cross-subject contrasts did not. These results indicate that OpenMIIR EEG supports modest but reproducible within-subject discrimination of music perception and cued imagery, with a linear-within-subject versus nonlinear-cross-subject generalization boundary, and they show why public EEG music data require leakage-aware validation and calibrated subject-generalization claims.

The development of the sleep-wake cycle reflects the progressive structural and functional maturation of the brain. However, the organization of neural dynamics during prematurity remains incompletely understood. In this study, we analyzed the EEG from 54 polysomnographic recordings obtained from 39 preterm infants, grouped according to postmenstrual age (PMA) into three categories: 30-31, 32-33 and 34-35 weeks. Lempel-Ziv Complexity (LZC) and Joint Lempel-Ziv Complexity (JLZC) of the electroencephalogram (EEG) were analyzed during active sleep (AS), quiet sleep (QS), and indeterminate sleep (IS). LZC computed from the raw, unfiltered recordings were significantly higher during QS than during AS and increased with PMA during AS. To further refine the analysis, LZC was also evaluated separately in the low-frequency (1-15.5 Hz) and high-frequency (16-30 Hz) EEG bands. In the low-frequency band, LZC was consistently higher during QS than during AS, an effect that was most pronounced in more immature groups. Furthermore, LZC increased with maturation particularly during AS. Sleep-state comparisons of LZC in the high-frequency EEG band also revealed higher values during QS than during AS across all PMA groups. Moreover, in contrast to the low-frequency band, LZC progressively decreased with advancing PMA both in AS and QS, suggesting that the neural mechanisms underlying low- and high-frequency EEG activity follow distinct maturational trajectories. Interestingly, larger LZC in the temporal cortex and interhemispheric differences were detected in the 32-33 PMA group. On the other hand, JLZC analysis revealed greater joint spatiotemporal dynamics across EEG channels during QS than during AS, with consistently higher JLZC values in temporal regions and lower in occipital regions. Together, these findings show that these complexity metrics distinguishes sleep states and captures maturational changes in EEG activity in preterm infants. These results provide novel insights into early brain development and suggest potential quantitative biomarkers of neonatal brain maturation.