# Effects of Ploidy on Relationship Between Outbreeding Response and Fitness in a Plant Selfing Species

## TL;DR

The study shows how ploidy levels affect outbreeding response and fitness in a selfing plant species, suggesting it could influence mating system evolution.

## Contribution

The paper demonstrates that outbreeding response is ploidy-dependent and functionally connected to fitness in a selfing plant species.

## Key findings

- Tetraploids showed the strongest and most consistent positive outbreeding responses, especially in gamete production.
- Increasing heterozygosity was linked to reduced phenotypic integration.
- Outbreeding response is functionally tied to fitness and may act as a selective force promoting outcrossing.

## Abstract

Outbreeding response, the phenotypic differences observed between selfed parental lines and their outcrossed offspring, can influence the evolution of selfing strategies. However, such effects remain poorly understood in noncrop species. We explored the phenotypic outbreeding response variation across ploidy levels in Erysimum incanum, a predominantly selfing plant complex with diploid, tetraploid, and hexaploid populations distributed across the Iberian Peninsula and Morocco. We performed controlled within‐population crosses to generate offspring with varying heterozygosity levels across ploidy types. We quantified individual, flower, and reproductive traits, and we estimated fitness components, and assessed trait modularity and phenotypic integration to see how heterozygosity affects trait coordination. Tetraploids showed the strongest and most consistently positive outbreeding responses, particularly in gamete production. Trait‐specific outbreeding responses were positively associated with fitness across ploidy levels. Increasing heterozygosity was linked to a reduction in phenotypic integration, suggesting a loosening of trait correlations. Results show that outbreeding response is ploidy‐dependent and functionally connected to fitness and it may act as a selective force promoting outcrossing in highly inbred lineages. We suggest that outbreeding response is a dynamic and evolvable trait, with implications for mating system transitions and diversification in selfing plant populations.

Outbreeding response is both ploidy‐dependent and functionally tied to fitness, highlighting its potential role in promoting outcrossing and driving mating system evolution in inbred plant populations.