Sparse Autoencoders Map Brain-LLM Alignment onto Cortical Semantic Topography
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Computer Science > Computation and Language
Title:Sparse Autoencoders Map Brain-LLM Alignment onto Cortical Semantic Topography
Abstract:Intermediate layers of large language models (LLMs) best predict human brain responses to language, one of the most robust findings in computational neurolinguistics, yet why remains mechanistically unexplained. We address this gap by bridging sparse autoencoders (SAEs) from mechanistic interpretability with neural encoding models, decomposing GPT-2 XL and Llama-3.1-8B into 16K-32K interpretable features per layer. A human-validated taxonomy ($\kappa \geq 0.74$) reveals that semantic features alone recover 94% of peak encoding performance ($r=0.285$), substantially exceeding variance-matched baselines ($p<0.001$, $d=1.31$). Beyond this aggregate dominance, we test a novel cortical topography prediction: five semantic subcategories derived a priori from three independent neuroscience programs should map onto distinct brain regions. A formal convergence test confirms this alignment (Spearman $\rho=0.72$, $p<0.001$; hypergeometric $p=0.007$), demonstrating that SAE-discovered features recapitulate known cortical semantic organization at a granularity inaccessible to prior methods. SAE features further predict human reading times beyond lexical controls ($\Delta\mathrm{logLik}=38.4$, $p<0.001$), and an exploratory prediction-error analysis provides preliminary evidence that the brain additionally encodes unexpected semantic content. Results generalize across English, Chinese, and French.
| Comments: | Accepted at CoNLL 2026. 20 pages (9 main + 1 limitations/acknowledgments + 3 references + 7 appendix), 5 figures, 20 tables |
| Subjects: | Computation and Language (cs.CL); Artificial Intelligence (cs.AI); Neurons and Cognition (q-bio.NC) |
| ACM classes: | I.2.7; I.2.6; J.3 |
| Cite as: | arXiv:2605.23035 [cs.CL] |
| (or arXiv:2605.23035v1 [cs.CL] for this version) | |
| https://doi.org/10.48550/arXiv.2605.23035
arXiv-issued DOI via DataCite (pending registration)
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