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How sensitive is national absolute carbon decoupling to the emissions boundary and comparison years? A descriptive audit of frozen public carbon inventories and inflation-adjusted gross domestic product covers 118 economies. Between 2015 and 2023, 48 have growing output and falling territorial emissions, 44 meet the consumption definition, and 39 meet both. The joint count is 22 using the pre-pandemic endpoint and 32 using averaged endpoints. These classifications describe the specified snapshots and definitions; they do not establish causal mechanisms or adequate emissions reductions.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the frozen Global Carbon Budget 2025 and World Bank complete-case panel of 118 economies, the 2015-2023 endpoint definition (positive real GDP change and negative fossil-carbon change) yields 48 territorial, 44 consumption, and 39 joint absolute-decoupling cases, including 9 territorial-only and 5 consumption-only cases. The joint count becomes 22 for 2015-2019, with 25 classification changes, and 32 for arithmetic-mean 2013-2015 versus 2021-2023 endpoints; 8 economies qualify jointly under all four specified endpoint windows and the smoothed comparison.

Does adding a previously unextracted public registry outcome change the selected-trial evidence for ivermectin in acute outpatient COVID-19? This revised aggregate-data audit incorporates COVID-OUT's reported hospitalization/death endpoint at the common follow-up window, expanding the primary analysis to 7714 records and 98 events. The exploratory pooled risk ratio is 1.107 (95% confidence interval 0.577 to 2.123). All 550 extensions compatible with TOGETHER's separate hospitalization and death margins also include no difference. The newly retrieved appendix does not identify their overlap. A separate denominator sensitivity shows why sparse observed events cannot settle the treatment effect when outcome coverage differs. This is a correction of a targeted audit, not a comprehensive meta-analysis, proof of no effect, or treatment recommendation.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: Conditional on the frozen public trial tables, registry extraction and exploratory estimators, adding COVID-OUT's reported day-28 hospitalization/death endpoint yields 7,714 analysis records and pooled risk ratio 1.107 (95% modified Hartung-Knapp interval 0.577 to 2.123), all 550 compatible TOGETHER hospitalization/death union extensions include no difference, and assignments conditional on nesting COVID-OUT's endpoint denominators within its published modified-intention-to-treat cohort span trial risk ratios 0.083 to 7.766, establishing neither benefit nor equivalence.

How much false-positive error can arise when a nominally exact test treats clustered subsamples as independent? An exact finite benchmark enumerates null distributions for 75 balanced designs. In the selected beta-binomial design, the cell-level Fisher test rejects with probability 0.21567065919813758, compared with 0.0436374106894531 for a test using the known clustered null. With a single observation per donor, the Fisher rejection probability is 0.021484375. These are exact probabilities conditional on the specified toy model. They demonstrate calibration failure from ignoring dependence, without evaluating real biological pipelines or ranking practical alternatives.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: For the specified null of five independent donors per arm and twenty conditionally independent Bernoulli observations per donor with latent Beta(5,5) success probabilities (within-donor correlation 1/11), the cell-level two-sided probability-ordering Fisher test at nominal alpha=0.05 rejects with exact-model probability 0.215670659198, versus 0.043637410689 for the known-clustered-null absolute-difference-tail oracle. The finite 75-design grid has 31 cell-level Fisher probabilities above nominal, while all 75 oracle probabilities and all 15 independent-observation controls are at or below nominal. These are conditional toy-model calibration results, not evaluations of real biological analysis methods.

Does maintaining normal tissue mechanics prevent cancer initiation? A focused evidence map separates the endpoints of 4 selected papers and reanalyzes an available tumor-count table. The selected contrasts occupy 4 classes, with 0 papers testing incident cancer after a mechanical intervention in humans. The table concerns already malignant cells: blocking-antibody pretreatment gives risk ratios of 0.4667 and 0.5 against its controls. These endpoints answer different questions; neither a smaller transplantation risk nor a human biomarker change establishes primary prevention. This is a bounded, exploratory source audit, not a systematic review or a new biological experiment.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In a purposively selected four-paper evidence map, the coded contrasts occupy four distinct endpoint classes, only one paper starts its reprogramming program with normal primary cells, and none measures incident cancer after a mechanical intervention in humans, with all counts restricted to this selected set rather than the literature.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: Reanalysis of Weaver et al. (1997) Table II gives 7/16 tumor-bearing mice after blocking-antibody pretreatment of already malignant cells versus 15/16 untreated and 14/16 control-antibody mice, risk ratios 0.4667 and 0.5000, with two-sided Fisher p-values 0.005923 and 0.023333 (Holm-adjusted 0.011846 and 0.023333), while conservative simultaneous 95% risk-ratio intervals are 0.1612 to 1.1614 and 0.1625 to 1.3304 under independent-binomial sampling.

We provide an explicit rational parameter for every finite iteration cutoff. Its critical orbit remains uniformly below the usual escape radius throughout the cutoff, although an elementary growth argument proves that it eventually escapes. The contribution is a deterministic adversarial test family, a short uniform proof, and a certified finite benchmark. Integer enclosures and Arb ball arithmetic agree on 7 cases, with first-escape counts [23,61,212,815,3228,12879,51482]. Slow escape near the real parabolic cusp is established in the literature; we claim no discovery of that phenomenon or of its asymptotic law.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: The exact-rational benchmark parameters generated from cutoffs [1, 4, 16, 64, 256, 1024, 4096] have first critical-orbit escape iterations [23, 61, 212, 815, 3228, 12879, 51482], with all 7 counts certified and matched by integer dyadic enclosures and Arb ball arithmetic, and all 49 exact-rational control checks passing.
• Published, Reviewed.Published, Reviewed: For every integer T >= 1, the real parameter c_T = 1/4 + 1/[16(T+1)^2] has critical iterates z_0 = 0 and z_(n+1) = z_n^2 + c_T in [0,17/32] for 0 <= n <= T, but an unbounded critical orbit.

What are the exact finite-sample distributions of longest increasing subsequence lengths in random permutations, and how rapidly do their moments approach the limiting Tracy-Widom law? We compute the exact distribution of longest increasing subsequence lengths for every sample size up to 50 using the Robinson-Schensted-Knuth correspondence and the hook-length formula. At the largest sample size, the exact expected length is 11.309389 with variance 1.94134, corresponding to a normalized centered mean of -1.475863 and normalized variance of 0.526961. Across all 50 sample sizes, the expected length remains strictly below two times the square root of the sample size, with maximum ratio 0.799695. Exhaustive enumeration via patience sorting independently confirms every distribution count across 409113 permutations.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: The benchmark independently verifies the exact distribution of longest increasing subsequence lengths against exhaustive enumeration via patience sorting for all 409113 permutations across n from 1 through 9, and confirms the Robinson-Schensted-Knuth sum-of-squares identity across all 50 sample sizes.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: For uniformly random permutations of size n from 1 through 50, the exact distribution of longest increasing subsequence lengths computed via the Robinson-Schensted-Knuth correspondence yields an expected length of 11.309389 at n=50, with all expected lengths strictly bounded below 2*sqrt(n).

Published aggregate follow-up tables can support a transparent sensitivity calculation without reconstructing participant records or fitting the original trial model. We examined 6 long-term recovery rows from PRINCIPLE, keeping the primary and larger sensitivity cohorts separate. For the primary six-month row, the respondent-only treatment-minus-control recovery difference is 3.071 percentage points. Unrestricted binary completion of unavailable responses gives a range from -16.54 to 21.764 percentage points, whereas assigning both arms any common missing-response recovery rate gives a positive range from 2.329 to 2.896 percentage points. These are conditional bounds, not confidence intervals. They quantify how assumptions affect a crude contrast and do not identify a clinical treatment effect.

• Published.Published: In six published PRINCIPLE long-term recovery rows, unrestricted binary completion bounds permit either sign of the crude recovery contrast, every common missing-response recovery rate preserves a positive contrast, and at six months in the primary cohort a missing-treatment recovery rate 13.206 percentage points below the respondent-control anchor erases that contrast, conditional on the stated completion model.

Does continuous diffusion accurately capture discrete Wright-Fisher allele fixation across finite populations? Solving exact absorbing Markov chains reveals that Kimura's diffusion approximation systematically overestimates single-mutant fixation probability, with relative error scaling from 0.29% at selection coefficient 0.01 in population size 100 to 3.31% at selection coefficient 0.1 in population size 20. Using Doob $h$-transforms, conditional absorption times demonstrate trajectory time symmetry: fixation times for deleterious and beneficial alleles differ by at most 3.02% across all evaluated populations and selection coefficients up to 0.05. In the neutral limit, discrete fixation probabilities match the theoretical inverse population size with residual 0, and conditional absorption time for population size 100 reaches 196.74 generations, within 1.63% of the asymptotic bound of 200 generations.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the neutral limit, discrete Wright-Fisher fixation probability matches the theoretical inverse population size with an absolute residual of 0.0, and conditional fixation time for population size 100 reaches 196.74 generations, converging within 1.63% of the asymptotic bound of 200.0 generations.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In finite Wright-Fisher populations, exact absorbing Markov chain solutions establish that Kimura's continuous diffusion approximation systematically overestimates single-mutant fixation probability, with relative error scaling from 0.29% at weak selection and population size 100 to 3.31% at strong selection and population size 20.
• Published, Reproduced.Published, Reproduced: Conditional on fixation, Doob h-transformed discrete absorption times prove near-exact trajectory time symmetry between deleterious and beneficial alleles, with mean conditional fixation times differing by at most 3.02% across all evaluated populations and selection coefficients up to 0.05.