Evidence map›Paper›PMID 39105302›Full record

ArticleJournal of evolutionary biology2024

Selection for greater dispersal in early life increases rate of age-dependent decline in locomotor activity and shortens lifespan.

B G Ruchitha, Nishant Kumar, Chand Sura, Sudipta Tung

Abstract read
In one paragraph

Article in Journal of evolutionary biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

4 authors.

B G RuchithaIntegrated Genetics and Evolution Laboratory (IGEL), Department of Biology, Ashoka University, Sonipat, Haryana 131029, India.
Nishant KumarIntegrated Genetics and Evolution Laboratory (IGEL), Department of Biology, Ashoka University, Sonipat, Haryana 131029, India.
Chand SuraIntegrated Genetics and Evolution Laboratory (IGEL), Department of Biology, Ashoka University, Sonipat, Haryana 131029, India.
Sudipta TungIntegrated Genetics and Evolution Laboratory (IGEL), Department of Biology, Ashoka University, Sonipat, Haryana 131029, India.ORCID 0000-0002-3201-3303

Funding

DBT-Wellcome Trust India Alliance IA/E/18/1/504347Wellcome TrustWellcome Trust India Alliance Early Career Fellowship #IA/E/18/1/504347
6 · The paper itself

Abstract

Locomotor activity is one of the major traits that is affected by age. Greater locomotor activity is also known to evolve in the course of dispersal evolution. However, the impact of dispersal evolution on the functional senescence of locomotor activity is largely unknown. We addressed this knowledge gap using large outbred populations of Drosophila melanogaster selected for increased dispersal. We tracked locomotor activity of these flies at regular intervals until a late age. The longevity of these flies was also recorded. We found that locomotor activity declines with age in general. However interestingly, the activity level of dispersal-selected populations never drops below the ancestry-matched controls, despite the rate of age-dependent decline in activity of the dispersal-selected populations being greater than their respective controls. The dispersal-selected population was also found to have a shorter lifespan as compared to its control, a potential cost of elevated level of activity throughout their life. These results are crucial in the context of invasion biology as contemporary climate change, habitat degradation, and destruction provide congenial conditions for dispersal evolution. Such controlled and tractable studies investigating the ageing pattern of important functional traits are important in the field of biogerontology as well.

Indexed as

Drosophila melanogasterLocomotionLongevityAgingAnimal DistributionAnimalsFemaleMaleSelection, Geneticdispersal evolutionDrosophila melanogasterevolution of ageingexperimental evolutionfunctional senescence

Identifiers

PMID39105302
PMCPMC7617655

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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.