Evidence map›Paper›PMID 32620168›Full record

ArticleBMC biology2020

The roles of hybridization and habitat fragmentation in the evolution of Brazil's enigmatic longwing butterflies, Heliconius nattereri and H. hermathena.

Darli Massardo, Nicholas W VanKuren, Sumitha Nallu, Renato R Ramos, Pedro G Ribeiro, Karina L Silva-Brandão, Marcelo M Brandão, Marília B Lion, André V L Freitas, Márcio Z Cardoso and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Hidden in plain sight: (Re)definition of a key lepidopteran color patterning gene.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  5. Population genomics and phylogeography ofEcology and evolution · 2022
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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

11 authors at 4 institutions in 2 countries.

Darli MassardoDepartment of Ecology & Evolution, The University of Chicago, Chicago, IL, USA.
Nicholas W VanKurenDepartment of Ecology & Evolution, The University of Chicago, Chicago, IL, USA. nvankuren@uchicago.edu.ORCID 0000-0001-8633-8851
Sumitha NalluDepartment of Ecology & Evolution, The University of Chicago, Chicago, IL, USA.
Renato R RamosDepartamento de Biologia Animal e Museu de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, SP, Brazil.
Pedro G RibeiroCentro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, SP, Brazil.
Karina L Silva-BrandãoCentro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André, SP, Brazil.
Marcelo M BrandãoCentro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, Campinas, SP, Brazil.
Marília B LionDepartamento de Ecologia, Universidade Federal do Rio Grande do Norte, Natal, RN, Brazil.
André V L FreitasDepartamento de Biologia Animal e Museu de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, SP, Brazil.
Márcio Z CardosoDepartamento de Ecologia, Universidade Federal do Rio Grande do Norte, Natal, RN, Brazil.
Marcus R KronforstDepartment of Ecology & Evolution, The University of Chicago, Chicago, IL, USA. mkronforst@uchicago.edu.
Universidade Estadual de Campinas (UNICAMP) · BRUniversity of Chicago · USUniversidade Federal do Rio Grande do Norte · BRUniversidade Federal do ABC · BR

Funding

Characterizing the Molecular Basis of Supergene Mimicry in ButterfliesR35GM131828 · NIGMS · UNIVERSITY OF CHICAGO · PI Marcus Kronforst · 2019 to 2026
$3.3M
Conselho Nacional de Desenvolvimento Científico e Tecnológico 163700/2017-6Conselho Nacional de Desenvolvimento Científico e Tecnológico 302585/2011-7Conselho Nacional de Desenvolvimento Científico e Tecnológico 303834/2015-3Conselho Nacional de Desenvolvimento Científico e Tecnológico 400242/2014-1Conselho Nacional de Desenvolvimento Científico e Tecnológico 563332/2010-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2011/00417-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2011/50225-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/16266-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/50260-6National Science Foundation DEB-1241056National Science Foundation DEB-1256742National Science Foundation IOS-1452648NIGMS NIH HHS R35 GM131828NIH HHS R35 GM131828United States Agency for International Development AID-OAA-A-11-00012
6 · The paper itself

Abstract

backgroundHeliconius butterflies are widely distributed across the Neotropics and have evolved a stunning array of wing color patterns that mediate Müllerian mimicry and mating behavior. Their rapid radiation has been strongly influenced by hybridization, which has created new species and allowed sharing of color patterning alleles between mimetic species pairs. While these processes have frequently been observed in widespread species with contiguous distributions, many Heliconius species inhabit patchy or rare habitats that may strongly influence the origin and spread of species and color patterns. Here, we assess the effects of historical population fragmentation and unique biology on the origins, genetic health, and color pattern evolution of two rare and sparsely distributed Brazilian butterflies, Heliconius hermathena and Heliconius nattereri.

resultsWe assembled genomes and re-sequenced whole genomes of eight H. nattereri and 71 H. hermathena individuals. These species harbor little genetic diversity, skewed site frequency spectra, and high deleterious mutation loads consistent with recent population bottlenecks. Heliconius hermathena consists of discrete, strongly isolated populations that likely arose from a single population that dispersed after the last glacial maximum. Despite having a unique color pattern combination that suggested a hybrid origin, we found no genome-wide evidence that H. hermathena is a hybrid species. However, H. hermathena mimicry evolved via introgression, from co-mimetic Heliconius erato, of a small genomic region upstream of the color patterning gene cortex.

conclusionsHeliconius hermathena and H. nattereri population fragmentation, potentially driven by historical climate change and recent deforestation, has significantly reduced the genetic health of these rare species. Our results contribute to a growing body of evidence that introgression of color patterning alleles between co-mimetic species appears to be a general feature of Heliconius evolution.

Indexed as

Biological EvolutionEcosystemGenomeHybridization, GeneticAnimalsBrazilButterfliesFemaleMaleWhole Genome SequencingHeliconiusHybridizationIntrogressionMimicryMutation loadPhylogenetics

Identifiers

PMID32620168
PMCPMC7334841
OpenAlexW3038672386

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.