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Shichang Liu

Publications and source records attributed to Shichang Liu.

3 recordsLinked to original sources

AgentLeak: Cloning Stronger LLM Agent Capabilities onto Weaker Agents Beyond Skill Stealing

Large language model (LLM) agents increasingly achieve long-horizon tasks by combining foundation models with explicit skills and implicit procedural knowledge acquired through execution. The resulting task-solving capabilities have become valuable proprietary assets, raising a new security question: can a substantially weaker attacker-controlled agent acquire the capabilities of a stronger proprietary agent through limited black-box interaction? Existing skill-stealing attacks recover explicit skill artifacts, yet we show that artifact leakage does not necessarily transfer capability: a weaker agent may possess the same skills but still fail because it lacks procedural behaviors implicitly realized by the stronger agent. Our key insight is that the skill execution gap itself forms a leakage surface, where missing behaviors are exposed through observable differences between successful victim executions and failed attacker executions. Based on this, we present AgentLeak, a black-box capability-cloning attack that identifies capability-critical behaviors from these execution differences and incorporates them into attacker-side skills, while keeping the attacker's model, harness, and tools unchanged. Across 20 task scenarios comprising 600 instances, diverse agent systems, and multiple backbone models, AgentLeak improves task pass rates by over 40% compared with direct skill reuse and recovers more than 80% of the victim--attacker capability gap. Our findings reveal a confidentiality risk in LLM agents: protecting explicit artifacts alone is insufficient, as observable execution behavior can leak the procedural knowledge required to reconstruct proprietary task-solving capabilities in low-capability and attacker-controlled agents.

cs.CR

Dynamic boxes fusion strategy in object detection

Object detection on microscopic scenarios is a popular task. As microscopes always have variable magnifications, the object can vary substantially in scale, which burdens the optimization of detectors. Moreover, different situations of camera focusing bring in the blurry images, which leads to great challenge of distinguishing the boundaries between objects and background. To solve the two issues mentioned above, we provide bags of useful training strategies and extensive experiments on Chula-ParasiteEgg-11 dataset, bring non-negligible results on ICIP 2022 Challenge: Parasitic Egg Detection and Classification in Microscopic Images, further more, we propose a new box selection strategy and an improved boxes fusion method for multi-model ensemble, as a result our method wins 1st place(mIoU 95.28%, mF1Score 99.62%), which is also the state-of-the-art method on Chula-ParasiteEgg-11 dataset.

cs.CV

Quantitative and functional post-translational modification proteomics reveals that TREPH1 plays a role in plant thigmomorphogenesis

Plants can sense both intracellular and extracellular mechanical forces and can respond through morphological changes. The signaling components responsible for mechanotransduction of the touch response are largely unknown. Here, we performed a high-throughput SILIA (stable isotope labeling in Arabidopsis)-based quantitative phosphoproteomics analysis to profile changes in protein phosphorylation resulting from 40 seconds of force stimulation in Arabidopsis thaliana. Of the 24 touch-responsive phosphopeptides identified, many were derived from kinases, phosphatases, cytoskeleton proteins, membrane proteins and ion transporters. TOUCH-REGULATED PHOSPHOPROTEIN1 (TREPH1) and MAP KINASE KINASE 2 (MKK2) and/or MKK1 became rapidly phosphorylated in touch-stimulated plants. Both TREPH1 and MKK2 are required for touch-induced delayed flowering, a major component of thigmomorphogenesis. The treph1-1 and mkk2 mutants also exhibited defects in touch-inducible gene expression. A non-phosphorylatable site-specific isoform of TREPH1 (S625A) failed to restore touch-induced flowering delay of treph1-1, indicating the necessity of S625 for TREPH1 function and providing evidence consistent with the possible functional relevance of the touch-regulated TREPH1 phosphorylation. Bioinformatic analysis and biochemical subcellular fractionation of TREPH1 protein indicate that it is a soluble protein. Altogether, these findings identify new protein players in Arabidopsis thigmomorphogenesis regulation, suggesting that protein phosphorylation may play a critical role in plant force responses.

q-bio.GN