Evidence map›Paper›PMID 30996674›Full record

ArticlePopulation ecology2018

Variance in animal longevity: contributions of heterogeneity and stochasticity.

Nienke Hartemink, Hal Caswell

Abstract read
In one paragraph

Article in Population ecology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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.

Nienke HarteminkInstitute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, P.O. Box 94248, 1090 GE Amsterdam, The Netherlands.
Hal CaswellInstitute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, P.O. Box 94248, 1090 GE Amsterdam, The Netherlands.ORCID 0000-0003-4394-6894

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Variance in longevity among individuals may arise as an effect of heterogeneity (differences in mortality rates experienced at the same age or stage) or as an effect of individual stochasticity (the outcome of random demographic events during the life cycle). Decomposing the variance into components due to heterogeneity and stochasticity is crucial for evolutionary analyses.In this study, we analyze longevity from ten studies of invertebrates in the laboratory, and use the results to partition the variance in longevity into its components. To do so, we fit finite mixtures of Weibull survival functions to each data set by maximum likelihood, using the EM algorithm. We used the Bayesian Information Criterion to select the most well supported model. The results of the mixture analysis were used to construct an age × stage-classified matrix model, with heterogeneity groups as stages, from which we calculated the variance in longevity and its components. Almost all data sets revealed evidence of some degree of heterogeneity. The median contribution of unobserved heterogeneity to the total variance was 35%, with the remaining 65% due to stochasticity. The differences among groups in mean longevity were typically on the order of 30% of the overall life expectancy. There was considerable variation among data sets in both the magnitude of heterogeneity and the proportion of variance due to heterogeneity, but no clear patterns were apparent in relation to sex, taxon, or environmental conditions.

Indexed as

Age-stage classified modelHeterogeneityIndividual stochasticityMixture modelsVariance in longevityWeibull distribution

Identifiers

PMID30996674
PMCPMC6435164

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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.