Evidence map›Paper›PMID 33557827›Full record

ArticleBMC biology2021

Beyond Drosophila: resolving the rapid radiation of schizophoran flies with phylotranscriptomics.

Keith M Bayless, Michelle D Trautwein, Karen Meusemann, Seunggwan Shin, Malte Petersen, Alexander Donath, Lars Podsiadlowski, Christoph Mayer, Oliver Niehuis, Ralph S Peters and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
9.8field-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

22 citing papers in PubMed, 63 citations in OpenAlex.

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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

17 authors at 8 institutions in 6 countries.

Keith M Bayless *Australian National Insect Collection, CSIRO National Research Collections Australia (NRCA), Acton, Canberra, ACT, Australia. keith.bayless@csiro.au.ORCID 0000-0002-8283-7052
Michelle D Trautwein *Department of Entomology, California Academy of Sciences, San Francisco, CA, USA.
Karen MeusemannAustralian National Insect Collection, CSIRO National Research Collections Australia (NRCA), Acton, Canberra, ACT, Australia.
Seunggwan ShinDepartment of Entomology & Plant Pathology, North Carolina State University, Raleigh, NC, USA.
Malte PetersenMax-Planck-Institut of Immunobiology and Epigenetics, Freiburg, Germany.
Alexander DonathCentre for Molecular Biodiversity Research (ZMB), Zoologisches Forschungsmuseum Alexander Koenig (ZFMK), Bonn, Germany.
Lars PodsiadlowskiCentre for Molecular Biodiversity Research (ZMB), Zoologisches Forschungsmuseum Alexander Koenig (ZFMK), Bonn, Germany.
Christoph MayerCentre for Molecular Biodiversity Research (ZMB), Zoologisches Forschungsmuseum Alexander Koenig (ZFMK), Bonn, Germany.
Oliver NiehuisDepartment of Evolutionary Biology & Ecology, Institute of Biology I, Albert Ludwig University of Freiburg, Hauptstraße 1, Freiburg i. Br., Germany.
Ralph S PetersCentre of Taxonomy and Evolutionary Research, Arthropoda Department, Zoological Research Museum Alexander Koenig, Bonn, Germany.
Rudolf MeierDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
Sujatha Narayanan KuttyDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
Shanlin LiuDepartment of Entomology, China Agricultural University, Beijing, People's Republic of China.
Xin ZhouDepartment of Entomology, China Agricultural University, Beijing, People's Republic of China.
Bernhard MisofZoological Research Museum Alexander Koenig (ZFMK), Bonn, Germany.
David K YeatesAustralian National Insect Collection, CSIRO National Research Collections Australia (NRCA), Acton, Canberra, ACT, Australia.
Brian M WiegmannDepartment of Entomology & Plant Pathology, North Carolina State University, Raleigh, NC, USA.
Zoological Research Museum Alexander Koenig · DECommonwealth Scientific and Industrial Research Organisation · AUChina Agricultural University · CNNational University of Singapore · SGNorth Carolina State University · USCalifornia Academy of Sciences · USMax Planck Institute of Immunobiology and Epigenetics · DEUniversity of Freiburg · DE

Funding

Division of Environmental Biology DEB-1257960
6 · The paper itself

Abstract

backgroundThe most species-rich radiation of animal life in the 66 million years following the Cretaceous extinction event is that of schizophoran flies: a third of fly diversity including Drosophila fruit fly model organisms, house flies, forensic blow flies, agricultural pest flies, and many other well and poorly known true flies. Rapid diversification has hindered previous attempts to elucidate the phylogenetic relationships among major schizophoran clades. A robust phylogenetic hypothesis for the major lineages containing these 55,000 described species would be critical to understand the processes that contributed to the diversity of these flies. We use protein encoding sequence data from transcriptomes, including 3145 genes from 70 species, representing all superfamilies, to improve the resolution of this previously intractable phylogenetic challenge.

resultsOur results support a paraphyletic acalyptrate grade including a monophyletic Calyptratae and the monophyly of half of the acalyptrate superfamilies. The primary branching framework of Schizophora is well supported for the first time, revealing the primarily parasitic Pipunculidae and Sciomyzoidea stat. rev. as successive sister groups to the remaining Schizophora. Ephydroidea, Drosophila's superfamily, is the sister group of Calyptratae. Sphaeroceroidea has modest support as the sister to all non-sciomyzoid Schizophora. We define two novel lineages corroborated by morphological traits, the 'Modified Oviscapt Clade' containing Tephritoidea, Nerioidea, and other families, and the 'Cleft Pedicel Clade' containing Calyptratae, Ephydroidea, and other families. Support values remain low among a challenging subset of lineages, including Diopsidae. The placement of these families remained uncertain in both concatenated maximum likelihood and multispecies coalescent approaches. Rogue taxon removal was effective in increasing support values compared with strategies that maximise gene coverage or minimise missing data.

conclusionsDividing most acalyptrate fly groups into four major lineages is supported consistently across analyses. Understanding the fundamental branching patterns of schizophoran flies provides a foundation for future comparative research on the genetics, ecology, and biocontrol.

Indexed as

Evolution, MolecularPhylogenyTranscriptomeAnimalsDrosophilaGene Expression ProfilingLarvaOvumPupaSequence Analysis, DNADipteraDrosophilidaePhylogenomicsTephritidaeTranscriptomes

Identifiers

PMID33557827
PMCPMC7871583
OpenAlexW3126451493

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.