Evidence map›Paper›PMID 35073910›Full record

ArticleBMC biology2022

The velvet worm brain unveils homologies and evolutionary novelties across panarthropods.

Christine Martin, Henry Jahn, Mercedes Klein, Jörg U Hammel, Paul A Stevenson, Uwe Homberg, Georg Mayer

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Serial Homology and Segment Identity in the Arthropod Head.Integrative organismal biology (Oxford, England) · 2022
    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

7 authors at 4 institutions in 1 country.

Christine MartinDepartment of Zoology, Institute of Biology, University of Kassel, 34132, Kassel, Germany. christine.martin@uni-kassel.de.ORCID http://orcid.org/0000-0003-0895-4936
Henry JahnDepartment of Zoology, Institute of Biology, University of Kassel, 34132, Kassel, Germany.
Mercedes KleinDepartment of Zoology, Institute of Biology, University of Kassel, 34132, Kassel, Germany.
Jörg U HammelInstitute of Materials Physics, Helmholtz-Zentrum hereon, 21502, Geesthacht, Germany.
Paul A StevensonPhysiology of Animals and Behaviour, Institute of Biology, University of Leipzig, 04103, Leipzig, Germany.
Uwe HombergDepartment of Biology, Animal Physiology, Philipps-Universität Marburg, 35043, Marburg, Germany.
Georg MayerDepartment of Zoology, Institute of Biology, University of Kassel, 34132, Kassel, Germany. georg.mayer@uni-kassel.de.
University of Kassel · DEHelmholtz-Zentrum Hereon · DELeipzig University · DEPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe evolution of the brain and its major neuropils in Panarthropoda (comprising Arthropoda, Tardigrada and Onychophora) remains enigmatic. As one of the closest relatives of arthropods, onychophorans are regarded as indispensable for a broad understanding of the evolution of panarthropod organ systems, including the brain, whose anatomical and functional organisation is often used to gain insights into evolutionary relations. However, while numerous recent studies have clarified the organisation of many arthropod nervous systems, a detailed investigation of the onychophoran brain with current state-of-the-art approaches is lacking, and further inconsistencies in nomenclature and interpretation hamper its understanding. To clarify the origins and homology of cerebral structures across panarthropods, we analysed the brain architecture in the onychophoran Euperipatoides rowelli by combining X-ray micro-computed tomography, histology, immunohistochemistry, confocal microscopy, and three-dimensional reconstruction.

resultsHere, we use this detailed information to generate a consistent glossary for neuroanatomical studies of Onychophora. In addition, we report novel cerebral structures, provide novel details on previously known brain areas, and characterise further structures and neuropils in order to improve the reproducibility of neuroanatomical observations. Our findings support homology of mushroom bodies and central bodies in onychophorans and arthropods. Their antennal nerve cords and olfactory lobes most likely evolved independently. In contrast to previous reports, we found no evidence for second-order visual neuropils, or a frontal ganglion in the velvet worm brain.

conclusionWe imaged the velvet worm nervous system at an unprecedented level of detail and compiled a comprehensive glossary of known and previously uncharacterised neuroanatomical structures to provide an in-depth characterisation of the onychophoran brain architecture. We expect that our data will improve the reproducibility and comparability of future neuroanatomical studies.

Indexed as

ArthropodsAnimalsBrainNervous SystemReproducibility of ResultsX-Ray MicrotomographyCentral bodyGlossaryMushroom bodyNervous systemNeuroanatomyOlfactory lobe

Identifiers

PMID35073910
PMCPMC9136957
OpenAlexW4207000015

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.