Back

Fixation of a homozygote and dynamical characterization of the Price equation

Garay, J.; Mori, T. F.

2026-04-24 evolutionary biology
10.64898/2026.04.22.720281 bioRxiv
Show abstract

Price equation and genotype dynamics are two methods for studying the fixation of one allele by natural selection in a diploid population. There are two strict monotonicity conditions that imply the fixation of one allele. The genotype dynamics is called Haldane monotone if the relative frequency of one allele strictly increases along all solutions of the genotype dynamics, so this allele is fixed. In this paper, we show that the genotype dynamics is Haldane monotone if and only if the right-hand side of the Price equation is always strictly positive. The other strict monotonicity condition requires that the relative frequency of a homozygote strictly increase according to the genotype dynamics. For example, in a model where the genotype dynamics is governed by interactions between individuals, the cost-accepting homozygote is fixed by natural selection if the other genotypes always receive a smaller average gain from all interactions than the cost-accepting homozygote. Both monotonicity conditions require that the interaction is not well-mixed in the population. These two conditions are not equivalent. In addition, we give a non-monotonicity condition, which also implies the fixation of a homozygote. The fixation of a homozygote depends on the phenotypic payoff of the interaction, the genotype-phenotype mapping, and the interaction scheme. In a sexual population, the interaction scheme of siblings depends on the mating system, and so do the conditions of fixation of the cost-accepting homozygote. We present examples showing that if we only change the monogamous mating system, assuming panmixing or mating assortativity, then the condition for the fixation of the cooperator homozygote is b > 2c and b > c, respectively.

Matching journals

The top 6 journals account for 50% of the predicted probability mass.

1
Bulletin of Mathematical Biology
84 papers in training set
Top 0.1%
12.4%
2
Journal of Mathematical Biology
37 papers in training set
Top 0.1%
10.5%
3
Journal of Theoretical Biology
144 papers in training set
Top 0.1%
8.4%
4
Theoretical Population Biology
47 papers in training set
Top 0.1%
8.4%
5
Evolution
199 papers in training set
Top 0.5%
7.2%
6
PLOS ONE
4510 papers in training set
Top 37%
3.7%
50% of probability mass above
7
Scientific Reports
3102 papers in training set
Top 36%
3.6%
8
BMC Ecology and Evolution
49 papers in training set
Top 0.6%
2.6%
9
Genetics
225 papers in training set
Top 2%
2.5%
10
Mathematical Biosciences
42 papers in training set
Top 0.4%
2.4%
11
The American Naturalist
114 papers in training set
Top 0.9%
2.1%
12
PLOS Computational Biology
1633 papers in training set
Top 13%
2.1%
13
Journal of Evolutionary Biology
98 papers in training set
Top 0.4%
1.9%
14
Royal Society Open Science
193 papers in training set
Top 2%
1.8%
15
Physical Review E
95 papers in training set
Top 0.6%
1.8%
16
Peer Community Journal
254 papers in training set
Top 2%
1.7%
17
Bioinformatics
1061 papers in training set
Top 7%
1.7%
18
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 33%
1.7%
19
GENETICS
189 papers in training set
Top 0.7%
1.5%
20
Entropy
20 papers in training set
Top 0.2%
1.3%
21
Journal of Computational Biology
37 papers in training set
Top 0.3%
1.3%
22
Ecology Letters
121 papers in training set
Top 1%
1.1%
23
eLife
5422 papers in training set
Top 53%
0.9%
24
Biology
43 papers in training set
Top 2%
0.8%
25
Ecology and Evolution
232 papers in training set
Top 4%
0.8%
26
Frontiers in Plant Science
240 papers in training set
Top 5%
0.7%
27
Cancers
200 papers in training set
Top 5%
0.7%
28
Proceedings of the Royal Society B: Biological Sciences
341 papers in training set
Top 7%
0.7%
29
Genes
126 papers in training set
Top 3%
0.7%
30
Physica A: Statistical Mechanics and its Applications
10 papers in training set
Top 0.3%
0.6%