Evidence map›Paper›PMID 32658967›Full record

ArticleMolecular biology and evolution2020

Allopatric and Sympatric Drivers of Speciation in Alviniconcha Hydrothermal Vent Snails.

Corinna Breusing, Shannon B Johnson, Verena Tunnicliffe, David A Clague, Robert C Vrijenhoek, Roxanne A Beinart

Abstract readComparative Study
In one paragraph

Article in Molecular biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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  7. Rapid speciation in the holopelagic ctenophorebioRxiv : the preprint server for biology · 2024
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  9. Review
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  16. Symbiont Community Composition inApplied and environmental microbiology · 2022
    Article
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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

6 authors.

Corinna BreusingGraduate School of Oceanography, University of Rhode Island, Narragansett, RI.
Shannon B JohnsonMonterey Bay Aquarium Research Institute, Moss Landing, CA.
Verena TunnicliffeDepartment of Biology and School of Earth and Ocean Sciences, University of Victoria, Victoria, BC, Canada.
David A ClagueMonterey Bay Aquarium Research Institute, Moss Landing, CA.
Robert C VrijenhoekMonterey Bay Aquarium Research Institute, Moss Landing, CA.
Roxanne A BeinartGraduate School of Oceanography, University of Rhode Island, Narragansett, RI.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite significant advances in our understanding of speciation in the marine environment, the mechanisms underlying evolutionary diversification in deep-sea habitats remain poorly investigated. Here, we used multigene molecular clocks and population genetic inferences to examine processes that led to the emergence of the six extant lineages of Alviniconcha snails, a key taxon inhabiting deep-sea hydrothermal vents in the Indo-Pacific Ocean. We show that both allopatric divergence through historical vicariance and ecological isolation due to niche segregation contributed to speciation in this genus. The split between the two major Alviniconcha clades (separating A. boucheti and A. marisindica from A. kojimai, A. hessleri, and A. strummeri) probably resulted from tectonic processes leading to geographic separation, whereas the splits between co-occurring species might have been influenced by ecological factors, such as the availability of specific chemosynthetic symbionts. Phylogenetic origin of the sixth species, Alviniconcha adamantis, remains uncertain, although its sister position to other extant Alviniconcha lineages indicates a possible ancestral relationship. This study lays a foundation for future genomic studies aimed at deciphering the roles of local adaptation, reproductive biology, and host-symbiont compatibility in speciation of these vent-restricted snails.

Indexed as

Genetic SpeciationHydrothermal VentsAnimalsFossilsGammaproteobacteriaGene Regulatory NetworksPhylogenyPhylogeographySnailsSymbiosisSympatryallopatric divergenceAlviniconchachemosynthetic symbiontsdeep-sea hydrothermal ventsecological isolationspeciation

Identifiers

PMID32658967
PMCPMC7743903

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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.