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Traffic forecasting benchmarks commonly fix the sensor set, although deployed sensing networks change their coverage over time. We present EvoXXLTraffic, a sensor-evolving extension of the XXLTraffic dataset family, with yearly sensor catalogs, persistent station IDs, flow matrices, and geographic graph snapshots across nine California PeMS districts, spanning up to 27 years. The benchmark separates all-sensor forecasting from supervised adaptation to sensors absent from the preceding year. We evaluate 13 baseline adaptations on PEMS04 with five seeds and PEMS05 with three seeds, and seven of them on the other seven districts with three seeds. Each yearly task uses 31 stored days, explicit observation masks, and chronological evaluation. Under the frozen configurations, PECPM has the lowest full-horizon mean MAE on both all-sensor and new-node populations on PEMS04, while Online-AN leads both populations on PEMS05. Among the seven methods run on every district, Online-AN has the lowest all-sensor mean MAE in eight of the nine districts, and Online-NN has the lowest new-node mean MAE in six. A matched control on PEMS05 and PEMS06 finds that training on the evolving catalog changes mean MAE on the sensors present in every 2018-2025 catalog by less than 1% in either direction. Method ordering depends on district, evaluation population, horizon, and metric, and seed variation does not establish statistical significance. The benchmark documents implementation adaptations and uses retrospective geographic graphs, limiting claims about original-paper rankings and prospective deployment. Inherited fixed-sensor gap and hourly/daily tasks provide complementary temporal settings. Code and results: https://github.com/cruiseresearchgroup/TSAS26-EvoXXLTraffic. Data: https://huggingface.co/datasets/yind7/EvoXXLTraffic.

Continuous Glucose Monitoring (CGM) can detect early metabolic subphenotypes (insulin resistance, IR; $β$-cell dysfunction), but population-scale deployment faces two coupled problems. First, the same physiological state appears through multiple views (CGM time series, venous OGTT, Glucodensity summaries), so single-view representations fail to transfer when deployment shifts the modality or setting. Second, baselines perform inconsistently across these shifts. Both problems point to one remedy: representations that abstract away from any single view to capture higher-level temporal and distributional structure. We propose CGM-JEPA, a self-supervised pretraining framework which predicts masked latent representations rather than raw values, yielding abstraction that transfers across modalities. X-CGM-JEPA adds a masked Glucodensity cross-view objective for complementary distributional information. We pretrain on $\sim$389k unlabeled CGM readings from 228 subjects and evaluate on two clinical cohorts ($N=27$ and $N=17$ public-release subsets) across three regimes (cohort generalization, venous-to-CGM transfer, home CGM) under 20-iteration $\times$ 2-fold cross-validation. X-CGM-JEPA ranks first or second on AUROC for both endpoints across all three regimes while no baseline does, exceeding the strongest baseline by up to $+6.5$ pp in cohort generalization and $+3.6$ pp in venous-to-CGM transfer (paired Wilcoxon, $p<0.001$). Under modality shift, it matches mean AUROC while redistributing toward weaker subgroups (ethnicity AUROC gap shrinks 25-54%); on sparse in-domain venous data, the distributional view lifts label-aware clustering (ARI $+39\%$, NMI $+40\%$). Code and weights: https://github.com/cruiseresearchgroup/CGM-JEPA