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This study challenges the reliability of sparse probing methods used to identify "hallucination neurons" in Large Language Models, revealing that such features often lack unique localization and exhibit low bootstrap stability. By proposing a rigorous five-step diagnostic protocol, the authors demonstrate that routine validation is essential to distinguish genuine mechanistic insights from statistical artifacts in high-dimensional feature spaces. These findings are critical for researchers aiming to build trustworthy, auditable AI systems through interpretability techniques.
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Hallucination Neurons and Where to Find Them: An Investigation into the existence of Hallucination Neurons

arXiv3 min read

arXiv:2609.29781v1 Announce Type: new Abstract: Interpretable machine learning for Large Language Models (LLMs) increasingly relies on sparse probing methods that identify small sets of neurons claimed to detect and causally influence behaviors such as factuality recall, safety alignment, and hallucination. These claims have important implications for model auditing and behavioral steering, yet they are rarely tested against known failure modes of $L_1$-regularized probing in correlated, high-dimensional feature spaces. We propose a five-step diagnostic protocol covering feature correlation, bootstrap stability, sparse versus dense ranking disagreement, intervention baselines, and cross-dataset evaluation as a minimum standard for sparse-neuron localization claims. We investigate prior work using our proposed approach, specifically on H-neurons using open-source LLMs across TriviaQA, BioASQ, and NQ-Open datasets. Our results demonstrate detection replicates across both models and datasets, and exceeds the original reported AUROC gaps for TriviaQA and BioASQ datasets. Gemma 3 4B consistently outperforms MedGemma 4B on matched datasets, with AUROC gaps of +0.311 versus +0.235 on TriviaQA, +0.474 versus +0.455 on BioASQ, and +0.128 versus +0.112 on NQ-Open respectively. Causal validation at $n = 500$ with five random seeds shows statistically significant effects beyond random same-layer baselines. At the same time, the diagnostic results indicate that the selected neurons are not uniquely localized. Across the three Gemma 3 4B settings, 19 of 22 selected H-Neurons have Pearson $|r| > 0.7$ with other features, bootstrap selections show only moderate stability, and sparse and dense rankings overlap only weakly. Our findings show that sparse predictive structure can coexist with non-unique neuron selection. Routine diagnostic validation is necessary to distinguish detection claims from localization claims in mechanistic interpretability.

Abstract:Interpretable machine learning for Large Language Models (LLMs) increasingly relies on sparse probing methods that identify small sets of neurons claimed to detect and causally influence behaviors such as factuality recall, safety alignment, and hallucination. These claims have important implications for model auditing and behavioral steering, yet they are rarely tested against known failure modes of $L_1$-regularized probing in correlated, high-dimensional feature spaces. We propose a five-step diagnostic protocol covering feature correlation, bootstrap stability, sparse versus dense ranking disagreement, intervention baselines, and cross-dataset evaluation as a minimum standard for sparse-neuron localization claims. We investigate prior work using our proposed approach, specifically on H-neurons using open-source LLMs across TriviaQA, BioASQ, and NQ-Open datasets. Our results demonstrate detection replicates across both models and datasets, and exceeds the original reported AUROC gaps for TriviaQA and BioASQ datasets. Gemma 3 4B consistently outperforms MedGemma 4B on matched datasets, with AUROC gaps of +0.311 versus +0.235 on TriviaQA, +0.474 versus +0.455 on BioASQ, and +0.128 versus +0.112 on NQ-Open respectively. Causal validation at $n = 500$ with five random seeds shows statistically significant effects beyond random same-layer baselines. At the same time, the diagnostic results indicate that the selected neurons are not uniquely localized. Across the three Gemma 3 4B settings, 19 of 22 selected H-Neurons have Pearson $|r| > 0.7$ with other features, bootstrap selections show only moderate stability, and sparse and dense rankings overlap only weakly. Our findings show that sparse predictive structure can coexist with non-unique neuron selection. Routine diagnostic validation is necessary to distinguish detection claims from localization claims in mechanistic interpretability.

Artificial Intelligence (cs.AI)

arXiv:2609.29781 [cs.AI]

(or arXiv:2609.29781v1 [cs.AI] for this version)

https://doi.org/10.48550/arXiv.2609.29781 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 355 words

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