Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
PLoS One
2019 Jan 01;141:e0210321. doi: 10.1371/journal.pone.0210321.
Show Gene links
Show Anatomy links
Population genetic structure of the Mediterranean horseshoe bat Rhinolophus euryale in the central Balkans.
Budinski I
,
Blagojević J
,
Jovanović VM
,
Pejić B
,
Adnađević T
,
Paunović M
,
Vujošević M
.
???displayArticle.abstract???
Migratory behaviour, sociality and roost selection have a great impact on the population structure of one species. Many bat species live in groups, and movements between summer and hibernation sites are common in temperate bats. The Mediterranean horseshoe bat Rhinolophus euryale is a cave-dwelling species that exhibits roost philopatry and undertakes seasonal movements which are usually shorter than 50 km. Its distribution in Serbia is restricted to karstic areas in western and eastern parts of the country, with a lack of known roosts between them. In this study, microsatellite markers were used to evaluate genetic variation in this species in the Central Balkans. Specifically, spatial genetic structuring between geographic regions and relatedness within different colony types were assessed. All analysed loci were polymorphic, and there was no significant inbreeding coefficient recorded. A moderate degree of genetic differentiation among the sampled colonies was found, and significant isolation by distance was recorded. Our results revealed that populations show a tendency to segregate into three clusters. Unexpectedly, populations from Montenegro and Eastern Serbia tended to group into one cluster, while populations from Western Serbia and Slovenia represented second and third cluster, respectively. The majority of variance was partitioned within colonies, and only a small but significant portion among clusters. Average relatedness within colony members was close to zero, did not differ significantly between the different colony types, and kinship is unlikely to be a major grouping mechanism in this species.
???displayArticle.pubmedLink???
30699143
???displayArticle.pmcLink???PMC6353099 ???displayArticle.link???PLoS One
Fig 1. Map of sampled localities.Locality numbers correspond to names in Table 1. triangle–hibernation roost, star–male summer roost, circle–nursery roost. Elevation in meters corresponding to the greyscale is given in legend.
Fig 2. Assignment probability of each individual to a given population.a) STRUCTURE plot under assumptions of K = 3. Population numbers correspond to names in Table 1; triangle–hibernation roost, star–male summer roost, circle–nursery roost. b) GENELAND admixture proportions. Labelled geographic regions are as in Table 1.
Burland,
Mating patterns, relatedness and the basis of natal philopatry in the brown long-eared bat, Plecotus auritus.
2001, Pubmed
Burland,
Mating patterns, relatedness and the basis of natal philopatry in the brown long-eared bat, Plecotus auritus.
2001,
Pubmed
Burland,
Seeing in the dark: molecular approaches to the study of bat populations.
2001,
Pubmed
Chapuis,
Microsatellite null alleles and estimation of population differentiation.
2007,
Pubmed
Estoup,
Homoplasy and mutation model at microsatellite loci and their consequences for population genetics analysis.
2002,
Pubmed
Excoffier,
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows.
2010,
Pubmed
Johnson,
Population Genetic Structure Within and among Seasonal Site Types in the Little Brown Bat (Myotis lucifugus) and the Northern Long-Eared Bat (M. septentrionalis).
2015,
Pubmed
Jost,
G(ST) and its relatives do not measure differentiation.
2008,
Pubmed
Kerth,
Mitochondrial DNA (mtDNA) reveals that female Bechstein's bats live in closed societies.
2000,
Pubmed
Kerth,
Colonization and dispersal in a social species, the Bechstein's bat (Myotis bechsteinii).
2005,
Pubmed
Meirmans,
Assessing population structure: F(ST) and related measures.
2011,
Pubmed
Peakall,
GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research--an update.
2012,
Pubmed
Pritchard,
Inference of population structure using multilocus genotype data.
2000,
Pubmed
Puechmaille,
Female mate choice can drive the evolution of high frequency echolocation in bats: a case study with Rhinolophus mehelyi.
2014,
Pubmed
Puechmaille,
The program structure does not reliably recover the correct population structure when sampling is uneven: subsampling and new estimators alleviate the problem.
2016,
Pubmed
Queller,
ESTIMATING RELATEDNESS USING GENETIC MARKERS.
1989,
Pubmed
Rambaut,
Posterior Summarization in Bayesian Phylogenetics Using Tracer 1.7.
2018,
Pubmed
Rivers,
Genetic population structure of Natterer's bats explained by mating at swarming sites and philopatry.
2005,
Pubmed
Rossiter,
Rangewide phylogeography in the greater horseshoe bat inferred from microsatellites: implications for population history, taxonomy and conservation.
2007,
Pubmed
Safi,
Comparative analyses suggest that information transfer promoted sociality in male bats in the temperate zone.
2007,
Pubmed
Simmons,
Evolution. An Eocene big bang for bats.
2005,
Pubmed
Strauss,
Preparation of genomic DNA from mammalian tissue.
2001,
Pubmed
Wang,
COANCESTRY: a program for simulating, estimating and analysing relatedness and inbreeding coefficients.
2011,
Pubmed
Weir,
ESTIMATING F-STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE.
1984,
Pubmed
Wilson,
Bayesian inference of recent migration rates using multilocus genotypes.
2003,
Pubmed