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This study reveals that current EEG foundation models fail to capture long-range temporal correlations, a critical feature for cross-population generalization in neurotechnology applications. The findings highlight a fundamental architectural limitation where spectral-input architectures mimic static noise patterns while discarding essential dynamic information required for robust zero-shot transfer across diverse cohorts. For AI researchers working on biomedical signal processing, this underscores the urgent need to redesign pooling mechanisms that preserve temporal order beyond short-patch reconstruction tasks.
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Foundation Models for EEG Are Blind to Long-Range Temporal Correlations: A Spectral-Temporal Dissociation Behind Their Cross-Population Fragility

arXiv3 min read

arXiv:2607.24834v1 Announce Type: cross Abstract: Objective. Electroencephalography (EEG) foundation models (FMs) are trained to reconstruct or contrastively align short patches, then pooled into a fixed embedding. We tested whether these embeddings retained the long-range temporal correlations (LRTC) quantified by the detrended-fluctuation-analysis (DFA) exponent of the alpha-band envelope, and whether it governs cross-population transfer. Approach. We probed five EEG FMs spanning raw-waveform and spectral-input architectures (REVE, LaBraM, BENDR, CBraMod, BIOT) on two out-of-distribution cohorts, comparing recovery of the DFA exponent against the static 1/f aperiodic slope. Order-preserving and residualization controls tested for pooling or aperiodic shadowing. A montage-harmonized, zero-shot transfer task compared the frozen embedding with the DFA exponent across three cohorts (adding a Western reference). Main results. None of the five FMs represented the LRTC in the temporal order. Raw-waveform models (REVE, LaBraM, BENDR) recovered neither the DFA exponent nor the 1/f slope (R^2 <= 0.12); for these three the probe is uninformative, so the dissociation is specific to the spectral-input models (CBraMod, BIOT), which recovered 1/f strongly (R^2 = 0.59-0.73) but not DFA across cohorts. A classical DFA feature recovered the exponent (R^2 = 0.32-0.38 against a 0.64 reliability ceiling), and LRTC was orthogonal to the aperiodic slope (r = -0.06). On cross-population transfer, the frozen REVE embedding did not beat chance (W to K, 0.45) and the dimensionless DFA exponent transferred directionally but not at family-wise significance; the other four did not uniformly replicate it. All five were dominated by a recording-site axis (decodable at 0.98-1.00 vs. 0.500 chance), whereas the DFA exponent they discard is site-robust (0.71).

Abstract:Objective. Electroencephalography (EEG) foundation models (FMs) are trained to reconstruct or contrastively align short patches, then pooled into a fixed embedding. We tested whether these embeddings retained the long-range temporal correlations (LRTC) quantified by the detrended-fluctuation-analysis (DFA) exponent of the alpha-band envelope, and whether it governs cross-population transfer. Approach. We probed five EEG FMs spanning raw-waveform and spectral-input architectures (REVE, LaBraM, BENDR, CBraMod, BIOT) on two out-of-distribution cohorts, comparing recovery of the DFA exponent against the static 1/f aperiodic slope. Order-preserving and residualization controls tested for pooling or aperiodic shadowing. A montage-harmonized, zero-shot transfer task compared the frozen embedding with the DFA exponent across three cohorts (adding a Western reference). Main results. None of the five FMs represented the LRTC in the temporal order. Raw-waveform models (REVE, LaBraM, BENDR) recovered neither the DFA exponent nor the 1/f slope (R^2 <= 0.12); for these three the probe is uninformative, so the dissociation is specific to the spectral-input models (CBraMod, BIOT), which recovered 1/f strongly (R^2 = 0.59-0.73) but not DFA across cohorts. A classical DFA feature recovered the exponent (R^2 = 0.32-0.38 against a 0.64 reliability ceiling), and LRTC was orthogonal to the aperiodic slope (r = -0.06). On cross-population transfer, the frozen REVE embedding did not beat chance (W to K, 0.45) and the dimensionless DFA exponent transferred directionally but not at family-wise significance; the other four did not uniformly replicate it. All five were dominated by a recording-site axis (decodable at 0.98-1.00 vs. 0.500 chance), whereas the DFA exponent they discard is site-robust (0.71).

Neurons and Cognition (q-bio.NC); Artificial Intelligence (cs.AI); Emerging Technologies (cs.ET); Machine Learning (cs.LG)

arXiv:2607.24834 [q-bio.NC]

(or arXiv:2607.24834v1 [q-bio.NC] for this version)

https://doi.org/10.48550/arXiv.2607.24834 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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