The Inference Report

Recent studies have reported clearly identifiable dynamical changes in the high-frequency range of EEG signals recorded during specific stimuli, such as visual or auditory inputs, or in cases of brain disorders like epileptic seizures. In this study, we utilized Dynamic Mode Decomposition (DMD) to extract consistent and persistent dynamical changes in the high-frequency band from the signals of neurologically relevant EEG channels. High-frequency DMD modes were employed as features, composing a feature table. Through post-processing, a random distribution test was performed, revealing that approximately 70% of the samples exhibited consistent high-frequency dynamics within the signal of a specific channel. Furthermore, classification experiments confirmed that the PCA components of the feature table that passed the test formed a consistent pattern that distinguished the alcohol-dependent group from the control group.

The ability to robustly maintain and update continuous variables is a hallmark of working memory. While classical continuous attractor networks suffer from severe fine-tuning fragility, standard artificial recurrent neural networks (RNNs) like GRUs and LSTMs typically fail to stably learn continuous manifolds, instead shattering the state space into discretized point attractors. To bridge this gap, we draw inspiration from divisive normalization, a canonical neural computation widely observed across cortical circuits, and propose the Recurrent Divisive Normalization Network (RDNN), a minimal and algebraically isolated model of dynamic division. Through dynamical systems analysis on canonical working memory tasks, we demonstrate that this biophysical constraint allows the network to converge to robust, high-fidelity slow manifolds. Furthermore, we analyze the gradient dynamics of divisive normalization during Backpropagation Through Time (BPTT), showing that it introduces an activity-dependent local gradient scaling. This scaling dampens parameter updates in highly active regimes, which empirically aligns with a significant self-compression of the network's effective rank, confining the recurrent dynamics to a tight, low-dimensional subspace while avoiding the optimization pathologies associated with explicit low-rank factorization. Finally, ablations demonstrate that while subtractive inhibition can maintain static memories, divisive normalization is mathematically essential to prevent manifold shattering under time-varying inputs. Our findings identify divisive normalization not merely as a biological artifact, but as a critical computational mechanism for learning high-fidelity continuous representations.

Human cortical organoids provide an experimentally accessible model of early neural circuit formation, yet whether their activity reflects structured information processing rather than spontaneous synchronization is unclear. We developed a graph-computational framework to quantify stimulus-evoked propagation. This includes stimulus-conditioned functional graphs, a graph-constrained dynamical (graph-neural-network) model used as a system-identification tool, a biological message-passing principle bounding integration depth by observable propagation depth, and a suite of graph-level metrics. We carried this program out in full on longitudinal HD-MEA recordings from three organoids. Once the true acquisition sampling rate and stimulus timing were recovered, the evoked response proved to be a fast, near-synchronous network burst with no measurable outward propagation (peak-latency vs. distance slope = 0). The propagation/integration-depth metrics (Deff ,reachability index, dmax) therefore do not apply, and per-day connectivity graphs were not reliably estimable at the available trial count, a negative result with methodological consequences for applying such metrics to organoid data. Reframing around synchrony, response-population size and shared variability revealed a control-validated phenomenon, i.e., repeated daily stimulation progressively depressed and spatially contracted the evoked response. That repeated stimulation reshapes organoid networks is established, but longitudinal designs in which every preparation is stimulated cannot separate this from developmental maturation. We break that confound with a developmentally-matched, stimulation-naive control, where at day 7, an organoid receiving its first-ever stimulation engaged 93% of the array, whereas organoids with five prior sessions engaged 10%.

LLMs are widely regarded as alien intelligences, systems whose cognitive operations are fundamentally unlike our own. Apparent similarities to human cognition are therefore often seen as the result of anthropomorphic projection. We argue that this framing is mistaken. LLMs clearly differ from humans in important respects, including their physical substrate, learning history, and the environments with which they interact. These differences make it all the more striking that contemporary LLM-based systems converge with human cognition on a number of principles of cognitive organization with longstanding support in cognitive science. We identify structural correspondences across five dimensions: inferential organization, computational architecture, representational structure, prediction-driven learning, and reinforcement-learning-like mechanisms supporting goal-directed action. These correspondences support a broader model of intelligent cognition in which core principles long used to explain human intelligence also characterize contemporary LLM-based systems.

Harnessing the potential of electroencephalography (EEG) for brain research is fundamentally limited by intrinsic noise and the diffuse projection of brain-generated activity over the scalp. The standard event-related potential (ERP) paradigm addresses this limitation by relying on repeated independent trials, albeit at the cost of moving away from naturalistic experimental conditions. As a more naturalistic alternative, we collected continuous EEG while participants watched short films and extracted potentials aligned to sharp cinematic transitions (cuts). We demonstrate that such transition-related potentials (TRPs) exhibit canonical ERP-like temporal structure associated with significant information processing. By comparing coherent films with scene-scrambled versions containing matched post-cut sensory input, we find that these responses are systematically shaped by narrative context. We then show that the cut-related EEG signature can be recovered directly from group-averaged continuous recordings with a compact deep neural network (DNN). The detector generalized across films and subject groups, and the resulting TRPs reproduced the main context-dependent effects observed for manually annotated cuts. These results indicate that narrative context leaves a measurable signature in EEG responses, that this signature can be detected directly in continuous recordings, and that such detections provide a semi-automated framework for analyzing how viewers process and understand film narratives. We propose that the method outlined here can be adapted to parse EEG responses to other forms of continuous stimulation, providing a general tool for probing experimental conditions that are closer to natural human experience.

Humans have always externalized thought onto tools, from the tally and the abacus to the map and, now, large language models. I model the agent, the tool, and the task as one dynamical system in which competence (what the user retains) and reliance (what the user outsources) co-evolve, and find that the outcome is bistable. Above a critical tool availability the competent state is destroyed and competence collapses toward a low dependent floor as the user outsources completely. Lowering availability does not reverse the collapse until a far lower threshold, so history of practice rather than the current tool fixes the state. Two users with the same present access can therefore occupy opposite and lasting states, one competent and one dependent, decided only by which they built first. The collapse threshold depends jointly on the competence a user brings to a task and on the tool's transparency, the fraction of its working a user can reconstruct. In the case where an agent faces an uncertain goal, a tool can cause agency itself to transfer to the tool and the human-agent becomes an agentic-instrument, irreversibly, because the tool's model is too large to internalize. The model is tested against several independent data sets, including GPS and map use, arithmetic expertise, and language models. These results reframe how tools should be built, how artificial intelligence is deployed, and what a tool-resistant education might require.