After the robustness pass, two additional bounded auxiliary stress checks were evaluated as diagnostics. These analyses do not change the primary hypothesis, do not refit the Catalog2 holdout, and do not introduce a second prediction claim. Their purpose is narrower: to test whether the same Catalog1-frozen CHC--FRC phase-load direction is specific relative to non-CHC controls and stable across declared holdout slices.
The specificity analysis is an adversarial-null board. It compares the target CHC--FRC frozen phase-load direction against physical, policy, random-orthogonal, cell-permuted, sign-shuffled, and bootstrap Catalog1 load families under the same Catalog2 matched-cell scoring surface. The target direction, denoted D0, ranks first on all declared primary specificity metrics: absolute Pearson alignment, absolute Spearman alignment, best-orientation sign agreement, and absolute projection. It also beats the declared random-orthogonal, cell-permuted, and sign-shuffled adversarial families at their family thresholds. The analysis label is
FRC-KP1-SPEC-ADVERSARIAL-NULL-COMPATIBLE. TeX source
\boxed{\code{FRC-KP1-SPEC-ADVERSARIAL-NULL-COMPATIBLE}}.
One policy decoy was blocked because it became constant or zero-norm under the frozen board; this is recorded as a blocked control rather than as supporting evidence.
The multi-slice analysis tests whether the primary Catalog2 alignment is concentrated in only one convenient region of the holdout. The scored slices cover the declared time, exposure, fluence, and dispersion-measure axes. Of 11 scored slices, 10 have the positive declared direction and 9 are classified strong. All four declared axes have positive slice counts. The analysis label is
FRC-KP1-MULTISLICE-STRESS-COMPATIBLE. TeX source
\boxed{\code{FRC-KP1-MULTISLICE-STRESS-COMPATIBLE}}.
The global slice reproduces the primary board values: phase-load correlation 0.889326696895743, fixed sign agreement 0.9032258064516129, Spearman correlation 0.6713709677419356, and exposure-scale transfer 0.7940469731995563.
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SPEC and MULTISLICE show that the constructed residual direction is not confined to one convenient slice under the stated diagnostics. They do not remove the predictive-density rejection and do not imply a CHIME selection-function result, a luminosity-function result, a global source-count law, or CHC empirical confirmation.