Evidence map›Paper›PMID 25575504›Full record

ArticleSystematic biology2015

Age-dependent speciation can explain the shape of empirical phylogenies.

Oskar Hagen, Klaas Hartmann, Mike Steel, Tanja Stadler

Erratum issuedAbstract read
In one paragraph

Article in Systematic biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Fossils improve extinction-rate estimates under state-dependent diversification models.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
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  6. Article
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  9. A vectorial tree distance measure.Scientific reports · 2022
    Article
  10. Article
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  12. Article
  13. Distance metrics for ranked evolutionary trees.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  14. How the past impacts the future: modelling the performance of evolutionarily distinct mammals through time.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  15. Article
  16. Article
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  18. Methods in ecology and evolution · 2018
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  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Oskar HagenInstitute of Integrative Biology, ETH Zürich, Universitätsstr. 16, 8092 Zürich, Switzerland; Institute for Marine and Antarctic Studies, University of Tasmania, Private Bag 49, Hobart, Tasmania 7001, Australia; Allan Wilson Centre for Molecular Ecology and Evolution, Biomathematics Research Centre, University of Canterbury, Christchurch 8140, New Zealand; and Department of Biosystems Science and Engineering, ETH Zürich, Mattenstrasse 26, 4058 Basel, Switzerland.
Klaas HartmannInstitute of Integrative Biology, ETH Zürich, Universitätsstr. 16, 8092 Zürich, Switzerland; Institute for Marine and Antarctic Studies, University of Tasmania, Private Bag 49, Hobart, Tasmania 7001, Australia; Allan Wilson Centre for Molecular Ecology and Evolution, Biomathematics Research Centre, University of Canterbury, Christchurch 8140, New Zealand; and Department of Biosystems Science and Engineering, ETH Zürich, Mattenstrasse 26, 4058 Basel, Switzerland.
Mike SteelInstitute of Integrative Biology, ETH Zürich, Universitätsstr. 16, 8092 Zürich, Switzerland; Institute for Marine and Antarctic Studies, University of Tasmania, Private Bag 49, Hobart, Tasmania 7001, Australia; Allan Wilson Centre for Molecular Ecology and Evolution, Biomathematics Research Centre, University of Canterbury, Christchurch 8140, New Zealand; and Department of Biosystems Science and Engineering, ETH Zürich, Mattenstrasse 26, 4058 Basel, Switzerland.
Tanja StadlerInstitute of Integrative Biology, ETH Zürich, Universitätsstr. 16, 8092 Zürich, Switzerland; Institute for Marine and Antarctic Studies, University of Tasmania, Private Bag 49, Hobart, Tasmania 7001, Australia; Allan Wilson Centre for Molecular Ecology and Evolution, Biomathematics Research Centre, University of Canterbury, Christchurch 8140, New Zealand; and Department of Biosystems Science and Engineering, ETH Zürich, Mattenstrasse 26, 4058 Basel, Switzerland Institute of Integrative Biology, ETH Zürich, Universitätsstr. 16, 8092 Zürich, Switzerland; Institute for Marine and Antarctic Studies, University of Tasmania, Private Bag 49, Hobart, Tasmania 7001, Australia; Allan Wilson Centre for Molecular Ecology and Evolution, Biomathematics Research Centre, University of Canterbury, Christchurch 8140, New Zealand; and Department of Biosystems Science and Engineering, ETH Zürich, Mattenstrasse 26, 4058 Basel, Switzerland tanja.stadler@bsse.ethz.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tens of thousands of phylogenetic trees, describing the evolutionary relationships between hundreds of thousands of taxa, are readily obtainable from various databases. From such trees, inferences can be made about the underlying macroevolutionary processes, yet remarkably these processes are still poorly understood. Simple and widely used evolutionary null models are problematic: Empirical trees show very different imbalance between the sizes of the daughter clades of ancestral taxa compared to what models predict. Obtaining a simple evolutionary model that is both biologically plausible and produces the imbalance seen in empirical trees is a challenging problem, to which none of the existing models provide a satisfying answer. Here we propose a simple, biologically plausible macroevolutionary model in which the rate of speciation decreases with species age, whereas extinction rates can vary quite generally. We show that this model provides a remarkable fit to the thousands of trees stored in the online database TreeBase. The biological motivation for the identified age-dependent speciation process may be that recently evolved taxa often colonize new regions or niches and may initially experience little competition. These new taxa are thus more likely to give rise to further new taxa than a taxon that has remained largely unchanged and is, therefore, well adapted to its niche. We show that age-dependent speciation may also be the result of different within-species populations following the same laws of lineage splitting to produce new species. As the fit of our model to the tree database shows, this simple biological motivation provides an explanation for a long standing problem in macroevolution.

Indexed as

Genetic SpeciationModels, BiologicalPhylogenyComputer SimulationTimeBirth–death processdiversificationmacroevolutionStochastic models

Identifiers

PMID25575504
PMCPMC4395845

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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.