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. 2024 Jun 10;78(8):1499–1510. doi: 10.1093/evolut/qpae060

Figure 2.

Figure 2

Fixation probabilities estimated from W–F simulations plotted as a function of inversion length for autosomal (A and B) and SLR-expanding inversions on Y chromosomes (C and D). Point shapes indicate different chromosome-arm-wide mutation rates relative to selection (i.e., different values of U), which influences the average deleterious mutation load carried by a standard-arrangement chromosome (U/(hs)). Dashed horizontal lines indicate the corresponding expected fixation probability for a neutral variant for the same population size, and hence correspond to values of 1/(𝟤𝑁) for autosomal inversions, and 𝟤/N for Y-linked inversions. In (C and D), we show fixation frequencies for all inversions (grey points), for only initially unloaded inversions (red points; i.e., the d=𝟢 inversion class), and the analytic approximation given by multiplying the probability that an inversion is initially mutation free by the effective initial frequency (unfilled points; i.e, 𝖯𝗋(fix𝑥)𝑓𝟢𝑞). Note: red points almost perfecty overlay grey points, but the few small discrepancies reflect rare additional fixations of initially (lightly) loaded inversions (where 𝑑>𝟢). Other parameter values were set to: h=0.25, s=0.01, and ntot=𝟣𝟢𝟦.