arXiv:2604.21131v1 Announce Type: cross
Abstract: AI-agent guardrails are memoryless: each message is judged in isolation, so an adversary who spreads a single attack across dozens of sessions slips past every session-bound detector because only the aggregate carries the payload. We make three contributions to cross-session threat detection.
(1) Dataset. CSTM-Bench is 26 executable attack taxonomies classified by kill-chain stage and cross-session operation (accumulate, compose, launder, inject_on_reader), each bound to one of seven identity anchors that ground-truth “violation” as a policy predicate, plus matched Benign-pristine and Benign-hard confounders. Released on Hugging Face as intrinsec-ai/cstm-bench with two 54-scenario splits: dilution (compositional) and cross_session (12 isolation-invisible scenarios produced by a closed-loop rewriter that softens surface phrasing while preserving cross-session artefacts).
(2) Measurement. Framing cross-session detection as an information bottleneck to a downstream correlator LLM, we find that a session-bound judge and a Full-Log Correlator concatenating every prompt into one long-context call both lose roughly half their attack recall moving from dilution to cross_session, well inside any frontier context window. Scope: 54 scenarios per shard, one correlator family (Anthropic Claude), no prompt optimisation; we release it to motivate larger, multi-provider datasets.
(3) Algorithm and metric. A bounded-memory Coreset Memory Reader retaining highest-signal fragments at $K=50$ is the only reader whose recall survives both shards. Because ranker reshuffles break KV-cache prefix reuse, we promote $mathrmCSR_prefix$ (ordered prefix stability, LLM-free) to a first-class metric and fuse it with detection into $mathrmCSTM = 0.7 F_1(mathrmCSDA@action, mathrmprecision) + 0.3 mathrmCSR_prefix$, benchmarking rankers on a single Pareto of recall versus serving stability.
Coordinated Temporal Dynamics of Glucocorticoid Receptor Binding and Chromatin Landscape Drive Transcriptional Regulation
Glucocorticoid receptor (GR) signaling elicits diverse transcriptional responses through dynamic and context-dependent interactions with chromatin. Here, we define a temporally resolved and mechanistically integrated framework


