摘要
Organoids are an increasingly central scientific platform for drug screening, disease modeling, and regenerative medicine. Because organoid form is closely tied to function, AI-driven image analysis has drawn intense interest, yet every existing organoid imaging study evaluates representations on a single dataset and no work has quantitatively compared representations across the breadth of public organoid datasets. We close this gap with \textbf{OrgBench}, a benchmark of 12 vision foundation models (VFMs) on 13 public organoid-imaging datasets spanning detection, segmentation, classification, and temporal outcome prediction. The benchmark reveals a structured domain gap: task-family winners shift across the benchmark and parameter count is a poor predictor of transfer. Building on this, we introduce \textbf{OrgFM}, a small bottleneck adapter that we continually pre-train on unlabeled organoid images while keeping a general-purpose vision transformer frozen. On the OrgBench task-family aggregates, OrgFM improves over its frozen base backbone. Layer- and feature-level interventions localize the gains to a small set of late-layer morphology-sensitive features: the adapter sparsely supplements, rather than replaces, the base representation. Together, this is the first cross-task, cross-backbone study of organoid imaging at scale; the OrgBench/OrgFM pairing establishes that the parameter-efficient adapter direction is a promising path for organoid representations and clarifies why it works.