Search arXivSearch

arXiv · 2607.27570

The evolution of cooperation under imperfect phenotypic recognition

Abstract

Phenotypic similarity is a classical mechanism for the evolution of cooperation. Most existing models assume a binary rule in which individuals cooperate only with others of the same phenotype. This assumption is biologically restrictive, since recognition and discrimination are often gradual rather than all-or-nothing. In this paper, we extend the multidimensional phenotype-space model of cooperation by allowing the probability of helping to decline with phenotypic distance. In a large population under weak selection with mutation in both strategy and phenotype, we derive a generalized threshold for selection to favor the abundance of cooperation and express it using a new Laplace-type transform. We show that this threshold decreases strictly as discrimination becomes sharper, meaning that exact phenotype matching is the most favorable limit within this family of recognition rules. We also show that the threshold decreases strictly with phenotype-space dimension, meaning that higher-dimensional phenotype spaces promote cooperation even when recognition is imperfect. Our asymptotic analysis further shows that low phenotype mutations strongly inhibit cooperation, whereas sufficiently high phenotype mutations drive the threshold toward its minimal value. However, high strategy mutation makes cooperation harder to maintain.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Dhaker Kroumi. 2026-07-30. The evolution of cooperation under imperfect phenotypic recognition. https://arxiv.org/abs/2607.27570

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

KEEP EXPLORING

Related papers

Mutation Order and Selection Shape Intratumor Heterogeneity in Tumor Evolution

Cancer progression often requires multiple driver mutations, but the same drivers may be acquired in different orders. How these pathways jointly shape tumor clonal structure remains unclear. We develop a multitype branching-process model in which malignant transformation requires two driver mutations, distinguishing malignant cells by mutation order and the independent transformation event that founded their clone. Under a successive exponential approximation, we establish point-process limits for pathway-specific clone sizes and derive a closed-form expression for the limiting expected Simpson's index of the combined malignant population. When both mutation orders yield malignant cells with the same net growth rate, the index decomposes into effective pathway weights, determined by mutation rates and birth-death dynamics at preceding stages, and within-pathway concentration terms, determined by intermediate-to-malignant growth-rate ratios. A driver's effect on heterogeneity thus depends critically on when it is acquired. A strong driver acquired early expands the intermediate lineage and increases the supply of independent malignant founders, whereas the same driver acquired last strengthens the growth and age advantage of early-founded malignant clones. Under additive fitness effects, these opposing mechanisms can produce a non-monotone relationship between selective advantage and clonal concentration. Threshold-like non-additive fitness effects can generate highly concentrated malignant populations, while order-dependent terminal fitness causes the faster-growing pathway to dominate asymptotically. These results show how mutation order, mutational accessibility, selection, and epistasis jointly determine lineage-level intratumor heterogeneity.

q-bio.PE

Phase transitions in microbial lineage trees

Microbial populations exhibit high cell-to-cell variability, which fundamentally shapes population behavior. A striking consequence is the existence of phase transitions, where small genetic or environmental changes trigger abrupt shifts in population dynamics. While biological phase transitions have often been proposed, connecting observed behavior to the underlying physics has remained challenging. We combine population genetics with statistical physics to show how phase transitions arise naturally in microbial populations. We highlight the existence of a first-order transition in a model of bacterial plasmid engineering and find a strict lower bound on the number of plasmids that can be stably maintained in a population.

q-bio.PE

Phylogenetic Inference and the Stickiness of Fréchet Means, via Precise Asymptotics of an Embedded Random Walk

A well-known phenomenon in statistical analyses of populations of phylogenetic trees in the Billera-Holmes-Vogtmann space is that the topology of the Fréchet mean tree can contain multifurcations (i.e., internal nodes with more than two children), which raises the practical question of whether this reflects a population-level branching structure (hard polytomy) or merely sampling variability in the data (soft polytomy). This is an instance of the more general phenomenon of "stickiness" in non-Euclidean statistics, whereby the sample Fréchet mean in certain non-positively curved stratified spaces becomes permanently trapped in a lower-dimensional stratum. In this work, we identify a particular multidimensional random walk embedded within the Fréchet mean process, and we show that the time at which stickiness occurs is determined by the largest last-passage time above zero of the coordinates of this random walk. Using this representation, we develop a fully nonparametric procedure for estimating the probability that trifurcations in a sample Fréchet mean tree will bifurcate at some future time if more observations are collected. Lastly, we apply our methodology to a problem in phylogenetics where we consider whether an observed trifurcation in the species tree of primates, glires, and tree shrews is genuinely trifurcated at the population level.

q-bio.PE