Evidence map›Paper›PMID 39913935›Full record

ArticleThe American naturalist2025

The Genetic Consequences of Range Expansion and Its Influence on Diploidization in Polyploids.

William W Booker, Daniel R Schrider

Abstract read
In one paragraph

Article in The American naturalist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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  3. Article
  4. Article
  5. Article
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  7. Article
  8. Whole-genome duplication increases genetic diversity and load in outcrossingProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

William W Booker
Daniel R Schrider

Funding

Deep learning for population geneticsR01HG010774 · NHGRI · UNIVERSITY OF OREGON · PI ANDREW D KERN · 2020 to 2026
$3.2M
Advancing evolutionary genetics through deep learningR35GM138286 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DANIEL R SCHRIDER · 2020 to 2026
$2.8M
NHGRI NIH HHS R01 HG010774NIGMS NIH HHS R35 GM138286
6 · The paper itself

Abstract

AbstractDespite newly formed polyploids being subjected to myriad fitness consequences, the relative prevalence of polyploidy, both contemporarily and in ancestral branches of the tree of life, suggests alternative advantages that outweigh these consequences. One proposed advantage is that polyploids may more easily colonize novel habitats, such as deglaciated areas. However, previous research conducted in diploids suggests that range expansion comes with a fitness cost, as deleterious mutations may fix rapidly on the expansion front. Here, we interrogate the potential consequences of expansion in polyploids by conducting spatially explicit forward-in-time simulations to investigate how ploidy and inheritance patterns impact the relative ability of polyploids to expand their range. We show that under realistic dominance models, autopolyploids suffer greater fitness reductions than diploids as a result of range expansion due to the fixation of increased mutational load that is masked in the range core. Alternatively, the disomic inheritance of allopolyploids provides a shield to this fixation, resulting in minimal fitness consequences. In light of this advantage provided by disomy, we investigate how range expansion may influence cytogenetic diploidization through the reversion to disomy in autotetraploids. We show that under a wide range of parameters investigated for two models of diploidization, disomy frequently evolves more rapidly on the expansion front than in the range core, and that this dynamic inheritance model has additional effects on fitness. Together our results point to a complex interaction among dominance, ploidy, inheritance, and recombination on fitness as a population spreads across a geographic range.

Indexed as

DiploidyGenetic FitnessModels, GeneticPolyploidyBiological EvolutionMutationallele surfingdiploidizationexpansion loadpolyploidpopulation geneticsrange expansion

Identifiers

PMID39913935
PMCPMC12469213

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.