Evidence map›Paper›PMID 37699868›Full record

ArticleNature communications2023

Evolutionary dynamics of genome size and content during the adaptive radiation of Heliconiini butterflies.

Francesco Cicconardi, Edoardo Milanetti, Erika C Pinheiro de Castro, Anyi Mazo-Vargas, Steven M Van Belleghem, Angelo Alberto Ruggieri, Pasi Rastas, Joseph Hanly, Elizabeth Evans, Chris D Jiggins and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
23.5field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Evolution of compound eye cell types shapes visual behaviors acrossbioRxiv : the preprint server for biology · 2026
    Article
  5. Transposable Element-Driven PIEZO Mutation Enhances Locust Flight in Plateau Hypoxia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Emerging tools to advance neuroethology in butterflies and moths.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Linking individual fitness to the evolution of cognition.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  19. Article
  20. 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

15 authors at 8 institutions in 7 countries.

Francesco CicconardiSchool of Biological Sciences, Bristol University, Bristol, United Kingdom. francicco@gmail.com.ORCID http://orcid.org/0000-0001-6509-6179
Edoardo MilanettiDepartment of Physics, Sapienza University, Piazzale Aldo Moro 5, 00185, Rome, Italy.
Erika C Pinheiro de CastroDepartment of Zoology, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-4731-3835
Anyi Mazo-VargasDepartment of Ecology and Evolutionary Biology, Cornell University, Ithaca, NY, 14853, USA.ORCID http://orcid.org/0000-0001-9644-2871
Steven M Van BelleghemDepartment of Biology, University of Puerto Rico, Rio Piedras, PR, Puerto Rico.ORCID http://orcid.org/0000-0001-9399-1007
Angelo Alberto RuggieriDepartment of Biology, University of Puerto Rico, Rio Piedras, PR, Puerto Rico.ORCID http://orcid.org/0000-0003-1427-2667
Pasi RastasInstitute of Biotechnology, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0003-2768-1339
Joseph HanlyDepartment of Biological Sciences, The George Washington University, Washington DC, WA, 20052, USA.ORCID http://orcid.org/0000-0002-9459-9776
Elizabeth EvansDepartment of Biology, University of Puerto Rico, Rio Piedras, PR, Puerto Rico.
Chris D JigginsDepartment of Zoology, University of Cambridge, Cambridge, United Kingdom.
W Owen McMillanSmithsonian Tropical Research Institute, Panama City, Panama.
Riccardo PapaDepartment of Biology, University of Puerto Rico, Rio Piedras, PR, Puerto Rico.ORCID http://orcid.org/0000-0002-7986-9993
Daniele Di MarinoDepartment of Life and Environmental Sciences, New York-Marche Structural Biology Center (NY-MaSBiC), Polytechnic University of Marche, Via Brecce Bianche, 60131, Ancona, Italy.
Arnaud MartinDepartment of Biological Sciences, The George Washington University, Washington DC, WA, 20052, USA.ORCID http://orcid.org/0000-0002-5980-2249
Stephen H MontgomerySchool of Biological Sciences, Bristol University, Bristol, United Kingdom. s.montgomery@bristol.ac.uk.ORCID http://orcid.org/0000-0002-5474-5695
University of Puerto Rico at Río Piedras · PRSmithsonian Tropical Research Institute · PAUniversity of Cambridge · GBCornell University · USGeorge Washington University · USItalian Institute of Technology · ITMarche Polytechnic University · ITUniversity of Helsinki · FI

Funding

SCIENCE AND TECHNOLOGY COMPETENCY & EDUCATION CORE (STCE)P20GM103475 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI Jose R. Rodriguez-Medina · 2012 to 2026
$52.9M
NIGMS NIH HHS P20 GM103475
6 · The paper itself

Abstract

Heliconius butterflies, a speciose genus of Müllerian mimics, represent a classic example of an adaptive radiation that includes a range of derived dietary, life history, physiological and neural traits. However, key lineages within the genus, and across the broader Heliconiini tribe, lack genomic resources, limiting our understanding of how adaptive and neutral processes shaped genome evolution during their radiation. Here, we generate highly contiguous genome assemblies for nine Heliconiini, 29 additional reference-assembled genomes, and improve 10 existing assemblies. Altogether, we provide a dataset of annotated genomes for a total of 63 species, including 58 species within the Heliconiini tribe. We use this extensive dataset to generate a robust and dated heliconiine phylogeny, describe major patterns of introgression, explore the evolution of genome architecture, and the genomic basis of key innovations in this enigmatic group, including an assessment of the evolution of putative regulatory regions at the Heliconius stem. Our work illustrates how the increased resolution provided by such dense genomic sampling improves our power to generate and test gene-phenotype hypotheses, and precisely characterize how genomes evolve.

Indexed as

ButterfliesAnimalsGenome SizeGenomicsPhenotypePhylogeny

Identifiers

PMID37699868
PMCPMC10497600
OpenAlexW4386692244

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.