Evidence map›Paper›PMID 40461816›Full record

ArticleCommunications biology2025

The ectoparasitic seal louse, Echinophthirius horridus, relies on a sealed tracheal system and spiracle closing apparatus for underwater respiration.

Anika Preuss, Thomas Schwaha, Alexander Kovalev, David Ebmer, Insa Herzog, Kristina Lehnert, Corvin Grass, Freya Sandberg, Elias Hamann, Marcus Zuber and 2 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Anika PreussDepartment of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Kiel, Germany. apreuss@zoologie.uni-kiel.de.ORCID http://orcid.org/0000-0003-0811-1613
Thomas SchwahaDepartment of Evolutionary Biology, University of Vienna, Schlachthausgasse 43, Vienna, Austria.
Alexander KovalevDepartment of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0002-9441-5316
David EbmerVienna Zoo, Maxingstraße 13b, Vienna, Austria.
Insa HerzogInstitute for Terrestrial and Aquatic Wildlife Research, University of Veterinary Medicine Hannover, Büsum, Germany.ORCID http://orcid.org/0000-0003-0534-0461
Kristina LehnertInstitute for Terrestrial and Aquatic Wildlife Research, University of Veterinary Medicine Hannover, Büsum, Germany.
Corvin GrassDepartment of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Kiel, Germany.
Freya SandbergDepartment of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Kiel, Germany.
Elias HamannKarlsruhe Institute of Technology, Institute for Photon Science and Synchrotron Radiation, Kaiserstr.12, Karlsruhe, Germany.
Marcus ZuberKarlsruhe Institute of Technology, Institute for Photon Science and Synchrotron Radiation, Kaiserstr.12, Karlsruhe, Germany.
Thomas van de KampKarlsruhe Institute of Technology, Institute for Photon Science and Synchrotron Radiation, Kaiserstr.12, Karlsruhe, Germany.ORCID http://orcid.org/0000-0001-7390-1318
Stanislav N GorbDepartment of Functional Morphology and Biomechanics, Zoological Institute, Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0001-9712-7953

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) GO 995 46-1
6 · The paper itself

Abstract

Marine mammals host a diverse array of parasites engaged in a continuous evolutionary arms race. However, our understanding of the biology of parasitic insects associated with marine mammals, particularly their adaptations to challenging marine environments, remains limited. The seal louse, Echinophthirius horridus, which infests true seals, is one of thirteen insect species capable of enduring prolonged dives in open seas. This ectoparasite has evolved several adaptations to withstand extreme conditions, such as low oxygen levels (hypoxia), temperature fluctuations, hydrostatic pressure, and strong drag forces during dives. To prevent drowning during their host's 20-35 min dives, seal lice have developed specialized respiratory mechanisms that allow them to survive in oxygen-poor waters and at depths up to 600 m. Advanced imaging techniques, including CLSM, SEM, synchrotron X-ray microtomography, and histological sectioning and 3D-reconstruction, have revealed a specialized spiracle closing apparatus for storing oxygen in their tracheal system. Furthermore, our buoyancy experiments showed that the lice consume oxygen under water and, with morphological data, provide what is to our knowledge the first direct evidence against plastron presence. These findings enhance our understanding of the physical adaptations of lice and their survival in extreme ecological conditions, contributing to broader ecological and evolutionary theories.

Indexed as

Seals, EarlessTracheaAnimalsDivingOxygenRespirationOxygen

Identifiers

PMID40461816
PMCPMC12134155

What OpenQuestion holds

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LicenceCC BY
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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.