#01Aug 21, 2026
cs.CV
A Modular Agent for Reliable and Auditable Spatial Relation Verification in CT Scans
Simon Vincent Abel, Heiko Hillenhagen, Michael Götz and 3 more
Reliable spatial understanding is an important prerequisite for future medical vision-language systems that aim to support radiological report generation and structured image understanding. While modern vision-language models (VLMs) show promising performance on many medical imaging tasks, recent evidence suggests they remain weak in controlled spatial reasoning and often fail to reliably ground spatial relations in image evidence. Given that radiological reasoning hinges on understanding the relative positions of anatomical structures and findings, this spatial weakness poses risks to diagnostic accuracy. We present a modular medical imaging agent for binary spatial relation verification in axial CT slices. Instead of directly predicting spatial answers end-to-end, the system decomposes the task into explicit stages: language parsing, anatomical localization, and deterministic geometric verification. Natural-language queries are converted into structured relation tuples, queried organs are localized with a YOLO-based detector, and the final spatial decision is computed from object centers using deterministic geometric rules. We evaluate the approach on the held-out MIRP spatial QA benchmark and compare it against representative end-to-end VLM baselines. The best-performing hybrid configuration reaches 94.1% accuracy and 94.2% F1, outperforming direct Qwen2-VL prompting by 42.5 percentage points in accuracy, while preserving interpretable intermediate representations and auditable reasoning stages. The results suggest that explicit modular spatial verification can serve as a promising building block for future report-oriented medical imaging agents.
#02Aug 21, 2026
cs.CV
Llama-Mobile: Efficient 2.7-Bit Quantization of VLMs
Luka Ribar, Jeevan Bhoot, Douglas Orr
Deploying vision-language models (VLMs) on mobile devices is challenging due to their significant memory and compute requirements. We present a framework for quantizing VLMs for efficient inference on resource-constrained hardware. Our approach combines a quantization pipeline that uses the model itself to generate training data and does not require access to the training setup, with a novel 2.7-bit-per-parameter format supporting efficient execution on Arm CPUs. We validate our approach by compressing the Llama 3.2 11B Vision Instruct model to 3.7 GB with 8-bit activations, preserving strong performance on a set of standard visual question answering tasks.
#03Aug 21, 2026
cs.CV
When does fusing hand-crafted knowledge with learned representations pay? A cost-normalized benchmark of stacking, substitution, and interference
Ahmad AlMughrabi, Albert Clop, Benjamin Busam and 2 more
Fusing prior knowledge with data-driven learning is attractive where data is scarce, yet no controlled account says when it helps, is redundant, or harms. We benchmark one fixed hand-crafted knowledge source, a pinned bank of Gabor targets injected only during training at $\sim$2\% overhead, against data-driven alternatives (SimCLR, SimSiam, DINO, ImageNet transfer, augmentation, learned teachers) under one frozen recipe with fixed subsets: 13 datasets, 9 backbones, 150 to 1.28M images, 32--224\,px, 2.5M--86M parameters ($\computeCells$ classification configurations over $\computeRuns$ runs, plus segmentation and detection transplants). Across the training-time combinations we measure, three outcomes recur (decision-level fusion differs). Different-\emph{currency} sources can stack: the prior composes with DeiT augmentation on attention backbones and is worth $+26$ points to ViT-B/16 at $224$\,px, $+6.7$ at twice that budget. Same-currency sources substitute: against effective self-supervised pretraining, the combination never usefully exceeds the better single source. Fusing at full strength into an already-informed initialization interferes in proportion to what it carries: ImageNet transfer, $-15$ to $-17$ points, removed by a weaker auxiliary weight. Frozen-feature diagnostics measured on each source alone separate these outcomes retrospectively but do not predict them: a rule built on them calls one of nine unseen pairs. At a practitioner's own label budget, the frozen-feature gain predicts the end-to-end gain to within $0.17$ points across 30 cells and seven datasets; the underlying decomposition, $Δ= G + \readout(\mathrm{base})$, holds in sign on $\auditRate\%$ of testable cells and is called an unseen backbone family's feature gain in advance. The project page is https://amughrabi.github.io/MomentAux.
#04Aug 21, 2026
cs.CV
On the Transferability of Agricultural Weed Detection Under Cross-Field Distribution Shift
Nikhilesh Prabhakar, Pranuthi Tenali, Wilfredo Abudeye Fernandez and 5 more
Accurate agricultural weed detection in real-world field conditions is essential for precision agriculture, enabling targeted intervention and reducing yield loss. Recent work has reported strong detection performance from UAV-based imagery across a range of crops, yet existing approaches evaluate within a single crop and field, leaving practitioners with little evidence that a model trained on one crop will generalize to a new field or crop type. In this work, we characterize where cross-dataset weed-localization performance degrades and which modeling choices recover it, reducing the need to relabel every new deployment field. We introduce a newly collected and annotated UAV image dataset for agricultural weed detection in cotton fields and use it alongside an existing soybean dataset collected under a similar protocol. Using these datasets, we evaluate the performance of several strategies for transferring a detector trained on one crop to another, comparing unsupervised domain adaptive object detection (DAOD) against pretraining on a domain-adjacent source dataset followed by few-shot fine-tuning on the target dataset. Our analysis spans target-domain label budgets from zero to the full target dataset, characterizing the trade-off between adaptation strategy and annotation effort. We find that few-shot fine-tuning with as few as 25 labeled target examples outperforms unsupervised DAOD in our cross-crop comparison, suggesting that source domain selection combined with modest target supervision is more productive than algorithmic sophistication in adaptation.
#05Aug 21, 2026
cs.AI
CellPath-Bench: A Multidimensional Benchmark for Whole-Slide Cellular Representations in Pathology Foundation Models
Bokai Zhao, Yiyang Zhang, Hanqing Chao and 6 more
Pathology foundation models (PFMs) are increasingly used as general-purpose backbones, yet existing benchmarks cannot systematically diagnose their whole-slide cellular representation capabilities, including the decodability of cell-type information and the transferability of such information across tissue sections, datasets, and anatomical organs. We introduce CellPath-Bench, a cellular-resolution benchmark that evaluates frozen PFMs themselves. Following quality control of 52 candidate Xenium datasets, we construct a panel of 25 spatially aligned H\&E--Xenium tissue sections spanning 11 organs and 7,079,283 cells, harmonized into fine- and coarse-grained taxonomies. CellPath-Bench samples frozen WSI feature maps at registered nuclear coordinates and evaluates them using standardized multiclass linear probes. Cell Representation Advantage (CRA) measures the within-section advantage of nucleus-anchored representations over patch-level mean pooling, while Cell Representation Transferability (CRT) characterizes the generalization of cell-type decodability across tissue sections, datasets, and organs. We benchmark 30 pathology-specific and general-purpose foundation models through 304,920 runs across spatial readouts, magnifications, taxonomic granularities, and evaluation protocols. The results reveal substantial model-dependent differences in cell-type decodability and its cross-domain generalization, yielding distinct multidimensional capability profiles. CellPath-Bench provides a standardized framework for auditing cellular information in frozen PFM representations.