Evidence map›Paper›PMID 31881939›Full record

ArticleBMC evolutionary biology2019

A genome-skimmed phylogeny of a widespread bryozoan family, Adeonidae.

Russell J S Orr, Marianne N Haugen, Björn Berning, Philip Bock, Robyn L Cumming, Wayne K Florence, Masato Hirose, Emanuela Di Martino, Mali H Ramsfjell, Maja M Sannum and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 15 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

14 authors at 7 institutions in 7 countries.

Russell J S OrrNatural History Museum, University of Oslo, Oslo, Norway. russell_orr@hotmail.com.ORCID 0000-0002-1972-1321
Marianne N HaugenCentre for Ecological and Evolutionary Synthesis, Department of Biosciences, University of Oslo, Oslo, Norway.
Björn BerningGeoscience Collections, Upper Austrian State Museum, Linz, Austria.
Philip BockMuseum Victoria, Melbourne, Victoria, Australia.
Robyn L CummingMuseum of Tropical Queensland, Townsville, Australia.
Wayne K FlorenceDepartment of Research and Exhibitions, Iziko Museums of South Africa, Cape Town, South Africa.
Masato HiroseSchool of Marine Biosciences, Kitasato University, Kanagawa, Japan.
Emanuela Di MartinoNatural History Museum, University of Oslo, Oslo, Norway.
Mali H RamsfjellNatural History Museum, University of Oslo, Oslo, Norway.
Maja M SannumNatural History Museum, University of Oslo, Oslo, Norway.
Abigail M SmithDepartment of Marine Science, University of Otago, Dunedin, New Zealand.
Leandro M VieiraDepartment of Zoology, Universidade Federal de Pernambuco, Recife, Brazil.
Andrea WaeschenbachDepartment of Life Sciences, Natural History Museum, London, UK.
Lee Hsiang LiowNatural History Museum, University of Oslo, Oslo, Norway. l.h.liow@nhm.uio.no.
University of Oslo · NOIziko Museums of South Africa · ZAKitasato University · JPMuseums Victoria · AUNatural History Museum · GBUniversidade Federal de Pernambuco · BRUniversity of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnderstanding the phylogenetic relationships among species is one of the main goals of systematic biology. Simultaneously, credible phylogenetic hypotheses are often the first requirement for unveiling the evolutionary history of traits and for modelling macroevolutionary processes. However, many non-model taxa have not yet been sequenced to an extent such that statistically well-supported molecular phylogenies can be constructed for these purposes. Here, we use a genome-skimming approach to extract sequence information for 15 mitochondrial and 2 ribosomal operon genes from the cheilostome bryozoan family, Adeonidae, Busk, 1884, whose current systematics is based purely on morphological traits. The members of the Adeonidae are, like all cheilostome bryozoans, benthic, colonial, marine organisms. Adeonids are also geographically widely-distributed, often locally common, and are sometimes important habitat-builders.

resultsWe successfully genome-skimmed 35 adeonid colonies representing 6 genera (Adeona, Adeonellopsis, Bracebridgia, Adeonella, Laminopora and Cucullipora). We also contributed 16 new, circularised mitochondrial genomes to the eight previously published for cheilostome bryozoans. Using the aforementioned mitochondrial and ribosomal genes, we inferred the relationships among these 35 samples. Contrary to some previous suggestions, the Adeonidae is a robustly supported monophyletic clade. However, the genera Adeonella and Laminopora are in need of revision: Adeonella is polyphyletic and Laminopora paraphyletically forms a clade with some Adeonella species. Additionally, we assign a sequence clustering identity using cox1 barcoding region of 99% at the species and 83% at the genus level.

conclusionsWe provide sequence data, obtained via genome-skimming, that greatly increases the resolution of the phylogenetic relationships within the adeonids. We present a highly-supported topology based on 17 genes and substantially increase availability of circularised cheilostome mitochondrial genomes, and highlight how we can extend our pipeline to other bryozoans.

Indexed as

AnimalsBiological EvolutionBryozoaEvolution, MolecularGenome, MitochondrialPhylogenyrRNA OperonSequence Analysis, DNACheilostome bryozoansGenome skimmingMitogenomePhylogenyrRNA

Identifiers

PMID31881939
PMCPMC6935126
OpenAlexW2998463509

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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.