Evidence map›Paper›PMID 34324748›Full record

ArticleMolecular ecology2021

The role of neutral and adaptive genomic variation in population diversification and speciation in two ground squirrel species of conservation concern.

Soraia Barbosa, Kimberly R Andrews, Amanda R Goldberg, Digpal S Gour, Paul A Hohenlohe, Courtney J Conway, Lisette P Waits

Open access · greenAbstract read
In one paragraph

Article in Molecular ecology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 14 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

7 authors at 2 institutions in 1 country.

Soraia BarbosaDepartment of Fish and Wildlife Sciences, College of Natural Resources, University of Idaho, Moscow, Idaho, USA.ORCID 0000-0001-7806-4256
Kimberly R AndrewsInstitute for Bioinformatics and Evolutionary Studies (IBEST), University of Idaho, Moscow, Idaho, USA.
Amanda R GoldbergDepartment of Fish and Wildlife Sciences, College of Natural Resources, University of Idaho, Moscow, Idaho, USA.
Digpal S GourDepartment of Fish and Wildlife Sciences, College of Natural Resources, University of Idaho, Moscow, Idaho, USA.
Paul A HohenloheInstitute for Bioinformatics and Evolutionary Studies (IBEST), University of Idaho, Moscow, Idaho, USA.ORCID 0000-0002-7616-0161
Courtney J ConwayU.S. Geological Survey, Idaho Cooperative Fish & Wildlife Research Unit, Department of Fish and Wildlife Sciences, College of Natural Resources, University of Idaho, Moscow, Idaho, USA.
Lisette P WaitsDepartment of Fish and Wildlife Sciences, College of Natural Resources, University of Idaho, Moscow, Idaho, USA.
University of Idaho · USUnited States Geological Survey · US

Funding

Genomics Resources Core (GRC)P30GM103324 · NIGMS · UNIVERSITY OF IDAHO · PI SETTLES, MATTHEW · 2013 to 2017
$5.0M
NIGMS NIH HHS P30 GM103324
6 · The paper itself

Abstract

Understanding the neutral (demographic) and adaptive processes leading to the differentiation of species and populations is a critical component of evolutionary and conservation biology. In this context, recently diverged taxa represent a unique opportunity to study the process of genetic differentiation. Northern and southern Idaho ground squirrels (Urocitellus brunneus-NIDGS, and U. endemicus-SIDGS, respectively) are a recently diverged pair of sister species that have undergone dramatic declines in the last 50 years and are currently found in metapopulations across restricted spatial areas with distinct environmental pressures. Here we genotyped single-nucleotide polymorphisms (SNPs) from buccal swabs with restriction site-associated DNA sequencing (RADseq). With these data we evaluated neutral genetic structure at both the inter- and intraspecific level, and identified putatively adaptive SNPs using population structure outlier detection and genotype-environment association (GEA) analyses. At the interspecific level, we detected a clear separation between NIDGS and SIDGS, and evidence for adaptive differentiation putatively linked to torpor patterns. At the intraspecific level, we found evidence of both neutral and adaptive differentiation. For NIDGS, elevation appears to be the main driver of adaptive differentiation, while neutral variation patterns match and expand information on the low connectivity between some populations identified in previous studies using microsatellite markers. For SIDGS, neutral substructure generally reflected natural geographical barriers, while adaptive variation reflected differences in land cover and temperature, as well as elevation. These results clearly highlight the roles of neutral and adaptive processes for understanding the complexity of the processes leading to species and population differentiation, which can have important conservation implications in susceptible and threatened species.

Indexed as

Genetics, PopulationGenomicsAnimalsGenotypeMicrosatellite RepeatsPolymorphism, Single NucleotideSciuridaeadaptationconservation geneticsgenomicsmammalsspeciationwildlife management

Identifiers

PMID34324748
PMCPMC8484062
OpenAlexW3139410581

What OpenQuestion holds

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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.