Evidence map›Paper›PMID 24567829›Full record

ArticleEcology and evolution2013

Investigating sex-specific dynamics using uniparental markers: West New Guinea as a case study.

Stefano Mona, Ernest Mordret, Michel Veuille, Mila Tommaseo-Ponzetta

Open access · goldAbstract read
In one paragraph

Article in Ecology and evolution, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 6 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

4 authors at 4 institutions in 2 countries.

Stefano MonaLaboratoire Biologie intégrative des populations, Ecole Pratique des Hautes Etudes 46 rue de Lille, 75007, Paris, France ; CNRS UMR 7205, Muséum National d'Histoire Naturelle Rue Buffon, 75005, Paris, France.
Ernest MordretLaboratoire Biologie intégrative des populations, Ecole Pratique des Hautes Etudes 46 rue de Lille, 75007, Paris, France ; CNRS UMR 7205, Muséum National d'Histoire Naturelle Rue Buffon, 75005, Paris, France.
Michel VeuilleLaboratoire Biologie intégrative des populations, Ecole Pratique des Hautes Etudes 46 rue de Lille, 75007, Paris, France ; CNRS UMR 7205, Muséum National d'Histoire Naturelle Rue Buffon, 75005, Paris, France.
Mila Tommaseo-PonzettaDepartment of Biology, University of Bari 70100, Bari, Italy.
Centre National de la Recherche Scientifique · FRÉcole Pratique des Hautes Études · FRMuséum national d'Histoire naturelle · FRUniversity of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial DNA (mtDNA) and Y chromosome (NRY) genetic markers have been often contrasted to investigate sex-specific dynamics. Traditionally, isolation by distance, intrapopulation genetic diversity and population differentiation are estimated from both markers and compared. Two possible sources of bias are often neglected. First, kilometric distances are frequently used as predictor of the connectivity between groups, hiding the role played by environmental features at a microgeographic scale. Second, the comparison of intrapopulation diversity and population differentiation between mtDNA and NRY is hampered by their different mutational mechanisms and rates. Here, we show how to account for these biases by analyzing from a different perspective a published dataset of eight West New Guinea (WNG) populations for which mtDNA control region sequences and seven linked NRY microsatellites had been typed. First, we modeled the connectivity among sampled populations by computing the number of days required to travel between groups. Then, we investigated the differences between the two sexes accounting for the molecular characteristics of the markers examined to obtain estimates on the product of the effective population size and the migration rate among demes (Nm). We achieved this goal by studying the shape of the gene genealogy at several sampling levels and using spatial explicit simulations. Both the direction and the rate of migration differ between male and females, with an Nm estimated to be >6 times higher in the latter under many evolutionary scenarios. We finally highlight the importance of applying metapopulation models when analyzing the genetic diversity of a species. We have applied the prediction of the sampling theory in a meta-population and we have corroborated our finding using spatial explicit simulations. Both approaches are fundamentally meant to deal with structured populations: we strongly believe in the importance of tacking structure into account when inferring the demographic history of a species.

Indexed as

Gene genealogymetapopulationpatrilocalityspatial simulationWest New Guinea

Identifiers

PMID24567829
PMCPMC3930047
OpenAlexW2048853041

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.