Sep 2026· Proceedings of the Thirty-Fifth International Joint Conference on Artificial Intelligence· pp. 735-743· 0 citations· 37 references
TL;DR
L DeLFE, a lightweight controlled detoxification approach that identifies specific toxic features across model layers and performs targeted interventions on them, and designs three feature-level strategies that adjust intervention timing and strength to reconstruct the target model’s original activations.
Abstract
Large Language Models (LLMs) powerful generative capabilities also pose significant risks, underscoring the need for effective detoxification methods to ensure safer deployment. Due to the polysemantic nature of LLM neurons, recent neuron intervention methods inevitably entangle unrelated concepts, compromising generation quality and interpretability. Sparse Autoencoders (SAEs) have opened new horizons for decomposing model activations into monosemantic features, offering interpretability and targeted feature-level steering. Empirical findings reveal that, despite capturing interpretable features, indiscriminate interventions on toxicity-related features expose the fragility of LLMs, achieving toxicity mitigation at the cost of degraded fluency. Building upon this finding, we propose DeLFE, a lightweight controlled detoxification approach that identifies specific toxic features across model layers and performs targeted interventions on them. DeLFE learns toxicity subspaces from label-guided SAE feature subsets to characterize toxic v.s. non-toxic activation patterns. When auto-completing a response token-by-token, DeLFE tracks the toxicity-triggering risks and steers toxic features away from the subspace via a flow-matching feature transformation. We further design three feature-level strategies that adjust intervention timing and strength to reconstruct the target model’s original activations. Extensive experiments demonstrate that our method achieves strong detoxification effectiveness while maintaining high generation quality across models of varying sizes and diverse base LLMs.
SPIRAL is presented, a layer-wise SAE analysis of BiRNA-BERT, a layer-wise SAE analysis of RNA language models where byte-pair tokenization breaks the one-token-one-nucleotide correspondence that nucleotide-level attribution assumes.
M. Hossain, MD. Roqunuzzaman Sojib, Md Toki Tahmid et al.· bioRxiv· 0 citations
Sparse autoencoder (SAE) features are typically discovered from how their activations co-vary with behaviour, yet they are often used through interventions such as steering or ablation. We take intervention attribution, the first-order effect of a specified intervention on the model output, as our estimand. For a broad...
A modular correction framework that augments pretrained LLMs with Activated LoRA (aLoRA) adapters and a context-aware routing mechanism to eliminate harms from misaligned model responses is proposed, offering a lightweight and efficient path toward safer and more controllable LLM deployments.
Robert C. Campbell, Momin Abbas, Muneeza Azmat et al.· 0 citations
This work introduces SCALPEL, a contrastive sparse autoencoder designed to learn more selective forget features and shows theoretically that contrastive training promotes target-selective features and that the selection score controls expected background knowledge perturbation.
The results suggest that architectural routing mechanisms may have negligible impact on core semantic understanding, with representational divergence confined to extreme structural margins.
Rithin Nagaraj, Rupa Laalasa Oruganti, Prerna Subhashchandra Kunder et al.· 0 citations
Sparse autoencoders (SAEs) are a central tool in mechanistic interpretability. However, existing SAEs are primarily trained per layer. The modeling subspace is therefore fixed by layer identity, independent of which token-layer states actually drive each prediction. We argue that this constraint contributes to several...
Qing-Wen Zeng, Ze-Hao Fu, Shu-Yu Meng et al.· 0 citations
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