Evidence map›Paper›PMID 41355290›Full record

ArticleMolecular ecology2025

Host Co-Occurrence and Population Size Explain Genetic Differentiation and Diversity in Seal Lice.

Ludmila Sromek, Kevin P Johnson, Mervi Kunnasranta, Aqqalu Rosing-Asvid, Britt-Marie Bäcklin, Aselle Tasmagambetova, Adylkhan Tovassarov, Olga Rusinek, Heather L Ziel, Ana Rubio-García and 1 more

Abstract read
In one paragraph

Article in Molecular ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

11 authors.

Ludmila SromekDepartment of Marine Ecosystems Functioning, Faculty of Oceanography and Geography, University of Gdansk, Gdynia, Poland.ORCID 0000-0002-3260-8032
Kevin P JohnsonIllinois Natural History Survey, Prairie Research Institute, University of Illinois, Champaign, Illinois, USA.
Mervi KunnasrantaDepartment of Environmental and Biological Sciences, University of Eastern Finland, Joensuu, Finland.
Aqqalu Rosing-AsvidGreenland Institute of Natural Resources, Nuuk, Greenland.
Britt-Marie BäcklinSwedish Museum of Natural History, Stockholm, Sweden.
Aselle TasmagambetovaCentral Asian Institute for Ecological Research, Almaty, Republic of Kazakhstan.
Adylkhan TovassarovCentral Asian Institute for Ecological Research, Almaty, Republic of Kazakhstan.
Olga RusinekBaikal Museum of the Siberian Branch of the Russian Academy of Sciences, Listvyanka, Russia.
Heather L ZielMarine Mammal Laboratory, Alaska Fisheries Science Center, National Oceanic and Atmospheric Administration, Seattle, Washington, USA.ORCID 0000-0001-7068-4418
Ana Rubio-GarcíaVeterinary, Care & Research Department, Seal Centre Pieterburen Foundation, Lauwersoog, the Netherlands.
Tommi NymanDepartment of Ecosystems in the Barents Region, Svanhovd Research Station, Norwegian Institute of Bioeconomy Research, Svanvik, Norway.ORCID 0000-0003-2061-0570

Funding

Betty Väänänen FoundationNarodowe Centrum Nauki 2019/32/C/NZ8/00335National Science Foundation DEB-1926919National Science Foundation DEB-2328118Nestori FoundationOskar Öflund FoundationRaija and Ossi Tuuliainen FoundationSocietas Pro Fauna et Flora Fennica
6 · The paper itself

Abstract

We studied the drivers of population-genetic structuring and genetic diversity in specialist parasites based on whole-genome resequencing data from 82 Echinophthirius horridus seal louse individuals sampled from 12 ecologically and behaviourally different phocine seal species, subspecies and populations across the Holarctic. We found that the main genetic disjunctions in E. horridus lice occur across seal host species and subspecies, with a further level of population subdivision emerging among host individuals within some populations. Endemic and relict landlocked seal (sub)species host the genetically most distinct louse populations, while lice associated with sympatric marine seals show signatures of occasional gene flow across hosts. Within the latter, the most extreme case is seen in the near-panmictic lice associated with northern European grey and harbour seals, which aggregate in shared rookeries and colonies. Although the louse and seal phylogenies were overall statistically significantly congruent, evidence for similar host shifts in the past is reflected in several conflicts in the phylogenetic trees of the lice and their hosts. Population-level mean heterozygosity and theta in seal lice varied considerably, and both measures of genetic variation were statistically significantly related to host population size. Taken together, our results support a non-adaptive model of parasite diversification, in which geographic and behavioural isolation among hosts drives parasite genetic differentiation, and genetic erosion in bottlenecked hosts cascades up to their specialist parasites. Our results provide new insights into processes that generate parasite diversity and trigger parallel losses of genetic diversity in endangered host-parasite systems.

Indexed as

Genetics, PopulationGenetic VariationHost-Parasite InteractionsPhthirapteraSeals, EarlessAnimalsGene FlowPhylogenyPopulation Densitycoevolutiongenetic diversityhost‐associated genetic differentiationhost–parasite interactionsinfrapopulation structure

Identifiers

PMID41355290
PMCPMC12717983

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