Algebraically invisible selection: fecundity–viability regimes acting on evolution algebras
Abstract
An evolution algebra encodes uniparental inheritance: its natural basis indexes genotypes and its structure constants \(a_{ij}\) record the rate at which a parent of type \(i\) produces offspring of type \(j\). The classical genetic-algebra literature excludes selection from its scope; this paper appears to give the first treatment of selection inside the algebra. A selection regime is a pair \((u,v)\) of positive weights acting on parental fecundity and offspring viability, deforming the algebra into the principal isotope with structure matrix \(\operatorname{diag}(u)M\operatorname{diag}(v)\). We prove that, modulo regimes acting trivially, the selected algebra is isomorphic to the original precisely when \(u_iv_i^2\) is constant across genotypes, the exponent reflecting the quadratic character of uniparental reproduction. We compute the moduli space on a fixed digraph, identify the cycle monomials of the bipartite support graph — cross ratios \(a_{ij}a_{kl}/(a_{il}a_{kj})\) in the generic case — as the exact invariants of arbitrary selection, and obtain a doubly stochastic normal form through an essentially unique balancing regime. Non-degenerate selection preserves all graph-determined structure but not non-basic ideals; lethal selection creates evolutionarily closed genotype classes. A three-genotype drug-resistance pathway illustrates the results, including an invisible regime that reverses the population’s long-run composition.
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How to Cite this Article
Mohammad Fathi Marashdeh, Algebraically invisible selection: fecundity–viability regimes acting on evolution algebras, Commun. Math. Biol. Neurosci., 2026 (2026), Article ID 103. https://doi.org/10.28919/cmbn/10225
Copyright © 2026 Mohammad Fathi Marashdeh. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.