Search bioRxiv⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2025.06.23.661088

Evolution of quantitative traits: exploring the ecological, social and genetic bases of adaptive polymorphism

Lehmann, L.·Mullon, C.
View original source ↗Export metadata ↓

Abstract

Adaptive polymorphisms in quantitative traits are characterised by the coexistence of distinct genetically encoded phenotypes maintained by selection. Such intraspecific genetic and phenotypic variation make a substantial contribution to biological diversity. Building on established results from invasion analysis, we analyse conditions under which adaptive polymorphism can emerge under long-term gradual evolution. We first note that, in general, fully characterising an adaptive polymorphism, including its number of morphs, trait values and frequencies, is a computationally hard problem. Nevertheless, standard invasion results reveal a unifying necessary condition for the gradual emergence of polymorphism: negative trait-dependent selection (NTDS), whereby the marginal fitness effect of increasing trait expression in a mutant depends negatively on the population-level trait expression, reflecting a negative interaction between mutant and population trait changes. We use NTDS as an organising principle to structure the pathways through which polymorphism can evolve. This is based on a decomposition of fitness that distinguishes production factors, the inputs to survival and reproduction that are endogenous to individuals, from regulating factors, the ecological, social or genetic inputs to fitness that are influenced in part by conspecifics. This decomposition allows us to clarify how NTDS arises across three broad classes of interactions: ecological, social and genetic; and to identify previously unrecognised adaptive polymorphisms in well-studied scenarios, including life-history, social preferences, and class-structured populations. More broadly, by integrating perspectives from population genetics, evolutionary ecology, adaptive dynamics, game theory and inclusive fitness theory, we aim to provide a common thread among the pathways through which selection favours intraspecific variation.

Source connections

Explore related subjects

evolutionary biologyPreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Lehmann, L., Mullon, C.. 2025-06-23. Evolution of quantitative traits: exploring the ecological, social and genetic bases of adaptive polymorphism. https://doi.org/10.1101/2025.06.23.661088

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

RELAX does not reproduce its own estimates at default settings, and its output does not show it

Selection-intensity estimates from RELAX are reported as a point value of K with a likelihood-ratio P. We report that, at default settings and on data of ordinary size, the program does not reproduce its own fits. Of 27 enzyme entries refitted under two optimiser configurations, none reproduced its log-likelihood to within 0.01 units; the median change was 103 units, the largest over 3,400, and four verdicts reversed. Eighty null orthologues reproduced none. A byte-identical command returned a distinct likelihood on every repetition, single-threaded, across three releases, and on alignments simulated under the fitted model, where 3.3 per cent of replicates reproduced. The documented random-number seed never reaches the generator when assigned on the command line, yet reads back as the value supplied. PAML localises the cause: its two-ratio model, without site classes, reproduced its log-likelihood for all 288 genes; its site-class models agreed for 27 to 67 per cent. The instability follows the mixture over sites, not the program. The output does not show it: 46 of 410 fits ended with a negative likelihood-ratio statistic, impossible under convergence, and 123 of 410 report a K re-estimated under a domain restriction rather than the unconstrained maximum. Of 234 published studies using RELAX, none reported a seed. Seeding while holding the thread count at one reproduced sixty of sixty runs on twenty genes under two releases; the seed alone reproduced none of five, and no documentation states the second condition. We recommend that fits be repeated and their dispersion published.

evolutionary biology↗
bioRxiv2026

Sequential accumulation of adaptive alleles forms an inversion supergene in deer mice

Supergenes are clusters of co-inherited loci that affect multiple or complex phenotypes. Despite the growing number of chromosomal inversions identified as supergenes in natural populations, their molecular basis and evolutionary history often remain obscure. Here, we identified two candidate genes, Slc45a2 and Npr3, within a 41-Mb inversion supergene in the deer mouse (Peromyscus maniculatus) that respectively drive darker coats and longer tails - two traits associated with forest adaptation. Mice homozygous for the inversion (inv/inv) exhibit elevated Slc45a2 expression in melanocytes relative to the congenic standard genotype (std/std), disrupting pheomelanin production. In parallel, downregulation of Npr3 in inv/inv mouse growth plates prolongs postnatal growth of caudal vertebrae, resulting in tail elongation. Population-level analyses further implicate that this supergene arose through the subsequent accumulation of the Npr3 allele within the inversion, rather than by capturing all beneficial mutations at its origin.

evolutionary biology↗
bioRxiv2026

Toxin structure shapes palatability in a chemically defended butterfly

The toxicity of chemical defences is well studied, but the potential contribution of compound structure to predator deterrence remains largely unexplored. Whether predation acts more strongly on toxicity or unpalatability remains largely untested, partly because few systems allow toxin structure to vary independently of quantity. Heliconius sara larvae provide such a system: those reared on Passiflora auriculata sequester cyclopentenyl cyanogenic glucosides (CGs), while those reared on P. biflora biosynthesise comparable quantities of aliphatic CGs. Using two invertebrate predators, Camponotus floridanus ants and Hierodula membranacea mantids, we tested whether this structural difference affects palatability independent of toxicity. Mantids rejected larvae with cyclopentenyl CGs more often than larvae with aliphatic CGs, despite no detectable difference in total CG content. This pattern was mirrored in extract-based assays with ants, independently of cyanide release: extracts with cyclopentenyl CGs remained deterrent, while extracts with aliphatic CGs did not differ in deterrence from water. Live larvae, by contrast, elicited similar responses from ants regardless of CG structure. These results show that variation in toxin structure can strongly affect palatability, with some compounds conferring greater protection than others. This demonstrates the importance of chemical structural diversity in the evolution of chemical defences.

evolutionary biology↗