Evidence map›Paper›PMID 39963932›Full record

ArticleEvolution & development2025

Developmental Plasticity and the Evolutionary Rescue of a Colonizing Mite.

Kathryn A Stewart, Isabel M Smallegange

Abstract read
In one paragraph

Article in Evolution & development, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Kathryn A StewartInstitute of Environmental Sciences (CML), Leiden University, Leiden, the Netherlands.ORCID 0000-0001-6132-6627
Isabel M SmallegangeSchool of Natural and Environmental Sciences, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0001-6218-7358

Funding

This work was funded by a VIDI grant no. 864.13.005 from the Dutch Research Council (NWO).
6 · The paper itself

Abstract

Plasticity, especially in small newly founded populations, can expose genetic variation to selection during the evolutionary rescue of populations, allowing individuals to achieve a phenotype with which they can survive. However, developmental plasticity can also enable organisms to accommodate perturbations, generating new phenotypic variation. We explored whether, at the start of a colonization event, phenotype dynamics follow a "selective" process in which plasticity fuels evolutionary rescue or whether they are due to developmental plasticity in a "generative" process. We investigated this using the bulb mite Rhizoglyphus robini, which expresses a facultative, juvenile dispersal phenotype (deutonymph) under unfavorable conditions and shows alternative adult male phenotypes: competitive fighters or benign scramblers that are expressed to mitigate food stress and which have higher levels of genetic heterozygosity than fighters. Mimicking colonization dynamics, we founded small, medium and large populations from deutonymphs on low or high food to test if scramblers were expressed earliest postcolonization within (i) the smallest founder populations to alleviate inbreeding (selective hypothesis), or (ii) the largest founder populations as a direct consequence of food stress is highest due to higher food competition (generative hypothesis). In line with the generative hypothesis under both food environments, scramblers were expressed at the earliest in the largest founder populations, which also tended to show the lowest growth at the start of the experiment and had the lowest ultimate population size. Our findings highlight the necessity to seek explanations of how developmental pathways likely influence evolutionary rescue patterns, starting with how resource limitation (stress) shapes adaptive responses during colonization.

Indexed as

AcaridaeAdaptation, PhysiologicalGenetic VariationAnimalsBiological EvolutionFemaleFertilityMaleMitesPhenotypePopulation Growtheco‐evolutionary dynamicsphoresypolyphenism

Identifiers

PMID39963932
PMCPMC11833757

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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.