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w(g0)<w(g1)<⋯<w(gL)w(g_0) < w(g_1) < \cdots < w(g_L)

Why this formula appears here

The reason is an ordering constraint. Under the standard assumption that a population moves by fixing one beneficial mutation at a time, a mutational path is accessible only if fitness increases at every single step: w(g0)<w(g1)<⋯<w(gL)w(g_0) < w(g_1) < \cdots < w(g_L). A single step that violates this inequality closes the entire path, regardless of how high the endpoint is. Sign epistasis is exactly the mechanism that produces such steps, and reciprocal sign epistasis — where each of two mutations is deleterious without the other and beneficial with it — is what creates genuinely separated local optima.

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ww

Symbol w

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g0g_0

Symbol g_0

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g1g_1

Symbol g_1

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gLg_L

Symbol g_L

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w(g0)<w(g1)<⋯<w(gL)w(g_0) < w(g_1) < \cdots < w(g_L)

Equation 2 · Evolution & Ecology

Fitness Landscapes and the Limits of the Metaphor

This equation states a bound: one expression must stay on the indicated side of the other under the article’s assumptions.

The reason is an ordering constraint. Under the standard assumption that a population moves by fixing one beneficial mutation at a time, a mutational path is accessible only if fitness increases at every single step: w(g0)<w(g1)<⋯<w(gL)w(g_0) < w(g_1) < \cdots < w(g_L). A single step that violates this inequality closes the entire path, regardless of how high the endpoint is. Sign epistasis is exactly the mechanism that produces such steps, and reciprocal sign epistasis — where each of two mutations is deleterious without the other and beneficial with it — is what creates genuinely separated local optima.

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