Evidence map›Paper›PMID 33148176›Full record

ArticleBMC evolutionary biology2020

Four myriapod relatives - but who are sisters? No end to debates on relationships among the four major myriapod subgroups.

Nikolaus U Szucsich, Daniela Bartel, Alexander Blanke, Alexander Böhm, Alexander Donath, Makiko Fukui, Simon Grove, Shanlin Liu, Oliver Macek, Ryuichiro Machida and 12 more

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

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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

22 authors.

Nikolaus U SzucsichDepartment of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria. nikola.szucsich@univie.ac.at.ORCID 0000-0002-8945-5153
Daniela BartelDepartment of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.
Alexander BlankeInstitute for Zoology, Biocenter, University of Cologne, D-50674, Cologne, Germany.
Alexander BöhmDepartment of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.
Alexander DonathCentre for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.
Makiko FukuiDepartment of Biology, Graduate School of Science and Engineering, Ehime University, Bunkyo-cho, Matsuyama, Ehime, 790-8577, Japan.
Simon GroveInvertebrate Zoology, Collections and Research Facility, Tasmanian Museum and Art Gallery, Rosny, Tasmania, 7018, Australia.
Shanlin LiuDepartment of Entomology, China Agricultural University, Beijing, 100193, People's Republic of China.
Oliver MacekDepartment of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.
Ryuichiro MachidaSugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira, Ueda, Nagano, 386-2204, Japan.
Bernhard MisofZoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.
Yasutaka NakagakiSugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira, Ueda, Nagano, 386-2204, Japan.
Lars PodsiadlowskiCentre for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.
Kaoru SekiyaSugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira, Ueda, Nagano, 386-2204, Japan.
Shigekazu TomizukaMatsunoyamamatsuguchi, Tokamachi, Niigata, 942-1411, Japan.
Björn M Von ReumontLOEWE Centre for Translational Biodiversity Genomics (LOEWE TBG), Senckenberganlage 25, 60325, Frankfurt, Germany.
Robert M WaterhouseDepartment of Ecology and Evolution, University of Lausanne and Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland.
Manfred WalzlDepartment of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.
Guanliang MengCentre of Taxonomy and Evolutionary Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.
Xin ZhouDepartment of Entomology, China Agricultural University, Beijing, 100193, People's Republic of China.
Günther PassDepartment of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.
Karen MeusemannCentre for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany. mail@karen-meusemann.de.

Funding

Austrian Science Fund P 20497-B17Austrian Science Fund P 23251-B17European Research Council 754290Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung PP00P3_170664
6 · The paper itself

Abstract

backgroundPhylogenetic relationships among the myriapod subgroups Chilopoda, Diplopoda, Symphyla and Pauropoda are still not robustly resolved. The first phylogenomic study covering all subgroups resolved phylogenetic relationships congruently to morphological evidence but is in conflict with most previously published phylogenetic trees based on diverse molecular data. Outgroup choice and long-branch attraction effects were stated as possible explanations for these incongruencies. In this study, we addressed these issues by extending the myriapod and outgroup taxon sampling using transcriptome data.

resultsWe generated new transcriptome data of 42 panarthropod species, including all four myriapod subgroups and additional outgroup taxa. Our taxon sampling was complemented by published transcriptome and genome data resulting in a supermatrix covering 59 species. We compiled two data sets, the first with a full coverage of genes per species (292 single-copy protein-coding genes), the second with a less stringent coverage (988 genes). We inferred phylogenetic relationships among myriapods using different data types, tree inference, and quartet computation approaches. Our results unambiguously support monophyletic Mandibulata and Myriapoda. Our analyses clearly showed that there is strong signal for a single unrooted topology, but a sensitivity of the position of the internal root on the choice of outgroups. However, we observe strong evidence for a clade Pauropoda+Symphyla, as well as for a clade Chilopoda+Diplopoda.

conclusionsOur best quartet topology is incongruent with current morphological phylogenies which were supported in another phylogenomic study. AU tests and quartet mapping reject the quartet topology congruent to trees inferred with morphological characters. Moreover, quartet mapping shows that confounding signal present in the data set is sufficient to explain the weak signal for the quartet topology derived from morphological characters. Although outgroup choice affects results, our study could narrow possible trees to derivatives of a single quartet topology. For highly disputed relationships, we propose to apply a series of tests (AU and quartet mapping), since results of such tests allow to narrow down possible relationships and to rule out confounding signal.

Indexed as

ArthropodsPhylogenyAnimalsTranscriptomeArthropod phylogenyConflictConfounding signalInternal rootingPhylogeneticsPhylogenomicsQuartet topologyRNA-SeqTranscriptomes

Identifiers

PMID33148176
PMCPMC7640414

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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.