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     Long Analysis Plan



    Experimental Design: 3×6 Mesocosm Test of Genetic vs Demographic Rescue

    Core question: Does adding genetically diverse immigrants (genetic rescue) outperform adding numerically equivalent low-diversity individuals (demographic augmentation), or any addition at all (control), on population growth, adaptive potential, and genomic dynamics over 6 generations?

    The design is powered by the temporal-autocovariance framework of Buffalo & Coop, which shows that neutral allele-frequency covariance across generations [Cov(Δpt, Δps)] rises under linked selection in proportion to the additive genetic variance for fitness, enabling joint estimation of VA(1) and Ne from time-series genotypes via a method-of-moments estimator validated by forward Wright–Fisher simulation across N = 100–1000 . This matters because real-world augmentation often fails: in Wisconsin martens, 68 translocated individuals contributed minimally to recruitment (0.57 ± 0.24) and juvenile survival (0.39 ± 0.21), with persistence driven by intrinsic vital rates .

    Design Specification

    • Units: 18 mesocosms (3 treatments × 6 replicates), randomized in a blocked layout; experimental unit = mesocosm.
    • Founder population: N = 100 census adults per mesocosm, drawn from a single inbred source stock to create low starting VA.
    • Treatments (G1 pulse, M = 10): (1) Genetic rescue — 10 unrelated immigrants from a divergent outbred stock; (2) Demographic augmentation — 10 full-sibs/clones matched to resident genotype (no added diversity, pure density); (3) Control — sham handling of 10 residents.
    • Sampling: Genotype 30 random individuals per mesocosm at each of G0–G5 (n = 30 × 6 × 18 = 3,240 genomes). Also census Ne proxies (sex ratio, variance in family size) and vital rates each generation.
    • Outcomes: (a) census growth rate λ; (b) Ne from temporal drift variance; (c) VA(1) from temporal autocovariance across ≥500 neutral markers; (d) fitness (survivorship × fecundity) of immigrant vs resident lineages.

    Expected signature: Genetic-rescue mesocosms should show immigrant alleles rising, elevated VA(1) via positive temporal autocovariance, and higher λ; demographic augmentation should elevate λ transiently but leave VA(1) and Ne unchanged. Control mesocosms calibrate drift-only decline in heterozygosity expected at Ne ≈ N = 100.

    Analysis Pipeline

    Compute per-locus Δpt = pt+1 − pt; estimate Ne = 1/(2·Var(Δp)) after correcting sampling noise for n = 30; regress lag-1 covariance of Δp against LD-to-selected-marker distance to extract VA(1) using the windowed genome-wide extension . Test treatment effects with mixed models (treatment fixed, mesocosm random, generation repeated).

    Critical Limitations & Blindspots

    (1) The autocovariance estimator assumes a closed, constant-size population with additive fitness effects and no migration — the immigration pulse violates the closed-population assumption and must be modeled explicitly. (2) n = 30 genotypes per mesocosm gives high sampling variance on Ne; allele-frequency estimates will be noisy for rare immigrant alleles (expected frequency 10/110 ≈ 0.09). (3) Six generations may be too short to separate immigrant swamping from drift in small mesocosms. (4) Mesocosm conditions differ from the wild; the marten study shows that demographic benefits of augmentation often do not translate to field fitness . (5) What would falsify the genetic-rescue hypothesis: immigrant allele loss with no VA(1) elevation and no λ advantage relative to demographic treatment.



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    Updated: October 15, 2026

     Top Data Sources ExportMCP



     Analysis Wizard



    Simulating Wright–Fisher temporal allele-frequency trajectories for the 18-mesocosm design and estimating Ne and VA(1) via the temporal autocovariance method-of-moments estimator to assess statistical power at n=30 genotypes per generation.



     Science Art


    Design Experiments: Implement a 3×6 replicates mesocosm experiment (Genetic rescue, Demographic augmentation, Control), start with census N=100 adults, introduce M=10 individuals in treatments, genotype 30 random individuals per mesocosm each generation (G0–G5), estimate allele-frequency trajectories, Ne, and VA(1) using temporal autocovariance—this directly tests genetic vs demographic effects in a replication-friendly design. Science Art

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