ArticleRoyal Society open science2020
Phenotypic plasticity of senescence in
Article in Royal Society open science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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.
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.
Who cites it
5 citing papers in PubMed, 9 citations in OpenAlex.
- Early-life, but not late-life, exposure to predator cues reduce the lifespan and reproductive output of freshwater snails.Oecologia · 2025Article
- The evolution of ageing: classic theories and emerging ideas.Biogerontology · 2024Review
- Rapamycin supplementation ofRoyal Society open science · 2023Article
- Level-dependent effects of predation stress on prey development, lifespan and reproduction in mites.Biogerontology · 2022Article
- Phenotypic plasticity of senescence inRoyal Society open science · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Recognising the nature of the predation risk, and responding to it accurately, is crucial to fitness. Yet, even the most accurate adaptive responses to predation risk usually entail costs, both immediate and lifelong. Rooting in life-history theory, we hypothesize that an animal can perceive the nuances of prey size and age selectivity by the predator and modulate its life history accordingly. We test the prediction that-contrary to the faster or earlier senescence under predation risk that increases with prey size and age-under predation risk that decreases with prey size and age either no senescence acceleration or even its deceleration is to be observed. We use two species of indeterminate growers, small crustaceans of the genus
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Registered trials
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.