Evidence map›Paper›PMID 31182814›Full record

ArticleNature ecology & evolution2019

Historical contingency shapes adaptive radiation in Antarctic fishes.

Jacob M Daane, Alex Dornburg, Patrick Smits, Daniel J MacGuigan, M Brent Hawkins, Thomas J Near, H William Detrich Iii, Matthew P Harris

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature ecology & evolution, 2019. 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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
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

36 citing papers in PubMed, 69 citations in OpenAlex.

  1. Physiology mediates transcontinental radiations of freshwater fishes.bioRxiv : the preprint server for biology · 2026
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  7. The many origins of extremophile fishes.Proceedings. Biological sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Jacob M DaaneDepartment of Marine and Environmental Sciences, Northeastern University Marine Science Center, Nahant, MA, USA. j.daane@northeastern.edu.ORCID http://orcid.org/0000-0003-3631-4514
Alex DornburgNorth Carolina Museum of Natural Sciences, Raleigh, NC, USA.
Patrick SmitsOrthopaedic Research Laboratories, Department of Orthopaedic Surgery, Boston Children's Hospital, Boston, MA, USA.
Daniel J MacGuiganDepartment of Ecology and Evolutionary Biology, Yale University, New Haven, CT, USA.
M Brent HawkinsOrthopaedic Research Laboratories, Department of Orthopaedic Surgery, Boston Children's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-5164-2893
Thomas J NearDepartment of Ecology and Evolutionary Biology, Yale University, New Haven, CT, USA.
H William Detrich IiiDepartment of Marine and Environmental Sciences, Northeastern University Marine Science Center, Nahant, MA, USA. w.detrich@northeastern.edu.ORCID http://orcid.org/0000-0002-0783-4505
Matthew P HarrisOrthopaedic Research Laboratories, Department of Orthopaedic Surgery, Boston Children's Hospital, Boston, MA, USA. harris@genetics.med.harvard.edu.ORCID http://orcid.org/0000-0002-7201-4693
Boston Children's Hospital · USNortheastern University · USAmerican Museum of Natural History · USNorth Carolina Museum of Natural Sciences · USYale University · US

Funding

Anatomical atlas and transgenic toolkit for late skull formation in zebrafishU01DE024434 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI FISHER, SHANNON, HARRIS, MATTHEW P · 2014 to 2018
$3.3M
NIDCR NIH HHS U01 DE024434
6 · The paper itself

Abstract

Adaptive radiation illustrates links between ecological opportunity, natural selection and the generation of biodiversity. Central to adaptive radiation is the association between a diversifying lineage and the evolution of phenotypic variation that facilitates the use of new environments or resources. However, is not clear whether adaptive evolution or historical contingency is more important for the origin of key phenotypic traits in adaptive radiation. Here we use targeted sequencing of >250,000 loci across 46 species to examine hypotheses concerning the origin and diversification of key traits in the adaptive radiation of Antarctic notothenioid fishes. Contrary to expectations of adaptive evolution, we show that notothenioids experienced a punctuated burst of genomic diversification and evolved key skeletal modifications before the onset of polar conditions in the Southern Ocean. We show that diversifying selection in pathways associated with human skeletal dysplasias facilitates ecologically important variation in buoyancy among Antarctic notothenioid species, and demonstrate the sufficiency of altered trip11, col1a2 and col1a1a function in zebrafish (Danio rerio) to phenocopy skeletal reduction in Antarctic notothenioids. Rather than adaptation being driven by the cooling of the Antarctic, our results highlight the role of historical contingency in shaping the adaptive radiation of notothenioids. Understanding the historical and environmental context for the origin of key traits in adaptive radiations extends beyond reconstructing events that result in evolutionary innovation, as it also provides a context in forecasting the effects of climate change on the stability and evolvability of natural populations.

Indexed as

Adaptation, PhysiologicalFishesAnimalsAntarctic RegionsBiodiversityHumansPhylogeny

Identifiers

PMID31182814
PMCPMC7147983
OpenAlexW2951960543

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.