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Mitochondrial DNA analysis reveals Holarctic homogeneity and a distinct Mediterranean lineage in the Golden eagle (Aquila chrysaetos)

Identifieur interne : 000455 ( Istex/Corpus ); précédent : 000454; suivant : 000456

Mitochondrial DNA analysis reveals Holarctic homogeneity and a distinct Mediterranean lineage in the Golden eagle (Aquila chrysaetos)

Auteurs : Carina Nebel ; Anita Gamauf ; Elisabeth Haring ; Gernot Segelbacher ; Alexandre Villers ; Frank E. Zachos

Source :

RBID : ISTEX:EF7F91C7070B86BB8B46FD8FEC1A389311CEF7C6

Abstract

The Golden eagle (Aquila chrysaetos) is among the most widespread of the birds of prey, covering basically the whole Palaearctic from Europe and North Africa through Asia and Japan, to the North American continent. Only few studies have addressed the species’ genetic structure and the consequences of its demographic history so far, and none of them has covered larger areas of the distribution range. Our present study aims at closing this gap. Based on 283 samples (mostly feathers collected in the field or from museum collections) across the species’ distribution, but with a focus on Europe, we uncover the phylogeography of the Golden eagle. Results imply a phylogeographic split between mainly Northern Europe, Continental Asia, Japan and North America on the one hand and Central–Southern Europe on the other. The observed pattern is likely to be caused by the Last Ice Age, when the population survived in two reproductively isolated glacial refugia. Repopulation of Northern Europe occurred from a presumed Asian refugium, whereas the Alpine range was probably repopulated from a refugium in the Mediterranean region. In Eastern Europe, the Mediterranean and Alpine region we find a co‐occurrence of both lineages that heavily influences the local genetic diversity. This pattern is unlike that in most other large raptors in which usually a western and an eastern Eurasian lineage have been recovered.

Url:
DOI: 10.1111/bij.12583

Links to Exploration step

ISTEX:EF7F91C7070B86BB8B46FD8FEC1A389311CEF7C6

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<correspondenceTo>Corresponding author. E‐mail:
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<title type="main">Mitochondrial
<fc>DNA</fc>
analysis reveals Holarctic homogeneity and a distinct Mediterranean lineage in the Golden eagle (
<i>Aquila chrysaetos</i>
)</title>
<title type="shortAuthors">C. Nebel
<i>et al</i>
.</title>
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<caption>
<p>
<b>Figure S1.</b>
Sequencing success rate of different types of material for the 402‐bp segment of the control region. The graph shows the success rate for the different types of material including small feathers, the umbilicus superior and inferior and tissue (muscle or footpad) in percentages. For the total number of samples, see Supporting Information, Table S2.</p>
<p>
<b>Figure S2.</b>
Map of Eurasia and North America; small dots represent successfully sequenced (both 402 and 350 bp) individuals. The Californian Golden eagles from Sonsthagen
<i>et al</i>
. (
<link href="#bij12583-bib-0056"></link>
) are represented as one large black circle. The percentages of Holarctic (black) and Mediterranean (grey) individuals in Central, Eastern and Southern Europe are shown in pie charts. Sample numbers for every pie chart (from east to west): Ukraine, Romania, Poland, Serbia and Hungary: 6 (H) and 4 (M); Austrian, German and Swiss Alps: 19 (H) and 91 (M); Italian Alps and Apennines: 3 (H) and 10 (M); French Alps: 0 (H) and 22 (M); Spain: 1 (H) and 15 (M).</p>
<p>
<b>Figure S3.</b>
Cumulative curves that show the increase of individuals and haplotypes in our Alpine data set over time. (for a total list see Table
<link href="#bij12583-tbl-0001"></link>
or Supporting Information, Table S1).</p>
<p>
<b>Table S1.</b>
Complete list of the 283 successfully sequenced Golden eagles according to region and country. M = Mediterranean Lineage, H = Holarctic Lineage. Haplotype numbers are the same as those in the network (Fig.
<link href="#bij12583-fig-0001"></link>
) and ML tree (Fig.
<link href="#bij12583-fig-0003"></link>
). The 350‐bp fragment was excluded from all statistics and only used for lineage identification. Taxonomy (subspecies) was assigned based on collection site.</p>
<p>
<b>Table S2.</b>
The complete data set (‘total sample’) and the successfully sequenced data set (
<i>N</i>
and %) by time and quality. ‘Other’ refers to material that was sampled at an unknown time, could not be classified as a small or large feather or comprised mixed types of materials (e.g. tissue and feather).</p>
<p>
<b>Table S3.</b>
Golden eagle haplotypes discovered in the present study, including information on time range, geographic occurrence and frequencies. The prefix of the haplotypes (M or H) depicts the genetic lineage they were assigned to.</p>
<p>
<b>Table S4.</b>
Estimated expansion times for Golden eagle populations. Times were estimated using the online spreadsheet tool of Schenekar & Weiss (
<link href="#bij12583-bib-0055"></link>
). Generation time (u) was assumed to be 12.5 years, the mutation rate was set to range from 4.54% (min) to 12.54% (max). The same mutation range was used for the Bayesian Skyline estimations. Fennoscandia showed significant deviation from an expansion event; therefore, no expansion time was calculated.</p>
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<p>The Golden eagle (
<i>Aquila chrysaetos</i>
) is among the most widespread of the birds of prey, covering basically the whole Palaearctic from Europe and North Africa through Asia and Japan, to the North American continent. Only few studies have addressed the species’ genetic structure and the consequences of its demographic history so far, and none of them has covered larger areas of the distribution range. Our present study aims at closing this gap. Based on 283 samples (mostly feathers collected in the field or from museum collections) across the species’ distribution, but with a focus on Europe, we uncover the phylogeography of the Golden eagle. Results imply a phylogeographic split between mainly Northern Europe, Continental Asia, Japan and North America on the one hand and Central–Southern Europe on the other. The observed pattern is likely to be caused by the Last Ice Age, when the population survived in two reproductively isolated glacial refugia. Repopulation of Northern Europe occurred from a presumed Asian refugium, whereas the Alpine range was probably repopulated from a refugium in the Mediterranean region. In Eastern Europe, the Mediterranean and Alpine region we find a co‐occurrence of both lineages that heavily influences the local genetic diversity. This pattern is unlike that in most other large raptors in which usually a western and an eastern Eurasian lineage have been recovered.</p>
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<title>Mitochondrial DNA analysis reveals Holarctic homogeneity and a distinct Mediterranean lineage in the Golden eagle (Aquila chrysaetos)</title>
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<name type="personal">
<namePart type="given">Carina</namePart>
<namePart type="family">Nebel</namePart>
<affiliation>Museum of Natural History Vienna, Vienna, Austria</affiliation>
<affiliation>E-mail: carina.nebel@gmail.com</affiliation>
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<affiliation>Department of Integrative Zoology, University of Vienna, Vienna, Austria</affiliation>
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<affiliation>Department of Integrative Zoology, University of Vienna, Vienna, Austria</affiliation>
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<abstract>The Golden eagle (Aquila chrysaetos) is among the most widespread of the birds of prey, covering basically the whole Palaearctic from Europe and North Africa through Asia and Japan, to the North American continent. Only few studies have addressed the species’ genetic structure and the consequences of its demographic history so far, and none of them has covered larger areas of the distribution range. Our present study aims at closing this gap. Based on 283 samples (mostly feathers collected in the field or from museum collections) across the species’ distribution, but with a focus on Europe, we uncover the phylogeography of the Golden eagle. Results imply a phylogeographic split between mainly Northern Europe, Continental Asia, Japan and North America on the one hand and Central–Southern Europe on the other. The observed pattern is likely to be caused by the Last Ice Age, when the population survived in two reproductively isolated glacial refugia. Repopulation of Northern Europe occurred from a presumed Asian refugium, whereas the Alpine range was probably repopulated from a refugium in the Mediterranean region. In Eastern Europe, the Mediterranean and Alpine region we find a co‐occurrence of both lineages that heavily influences the local genetic diversity. This pattern is unlike that in most other large raptors in which usually a western and an eastern Eurasian lineage have been recovered.</abstract>
<note type="additional physical form">Figure S1. Sequencing success rate of different types of material for the 402‐bp segment of the control region. The graph shows the success rate for the different types of material including small feathers, the umbilicus superior and inferior and tissue (muscle or footpad) in percentages. For the total number of samples, see Supporting Information, Table S2. Figure S2. Map of Eurasia and North America; small dots represent successfully sequenced (both 402 and 350 bp) individuals. The Californian Golden eagles from Sonsthagen et al. () are represented as one large black circle. The percentages of Holarctic (black) and Mediterranean (grey) individuals in Central, Eastern and Southern Europe are shown in pie charts. Sample numbers for every pie chart (from east to west): Ukraine, Romania, Poland, Serbia and Hungary: 6 (H) and 4 (M); Austrian, German and Swiss Alps: 19 (H) and 91 (M); Italian Alps and Apennines: 3 (H) and 10 (M); French Alps: 0 (H) and 22 (M); Spain: 1 (H) and 15 (M). Figure S3. Cumulative curves that show the increase of individuals and haplotypes in our Alpine data set over time. (for a total list see Table or Supporting Information, Table S1). Table S1. Complete list of the 283 successfully sequenced Golden eagles according to region and country. M = Mediterranean Lineage, H = Holarctic Lineage. Haplotype numbers are the same as those in the network (Fig. ) and ML tree (Fig. ). The 350‐bp fragment was excluded from all statistics and only used for lineage identification. Taxonomy (subspecies) was assigned based on collection site. Table S2. The complete data set (‘total sample’) and the successfully sequenced data set (N and %) by time and quality. ‘Other’ refers to material that was sampled at an unknown time, could not be classified as a small or large feather or comprised mixed types of materials (e.g. tissue and feather). Table S3. Golden eagle haplotypes discovered in the present study, including information on time range, geographic occurrence and frequencies. The prefix of the haplotypes (M or H) depicts the genetic lineage they were assigned to. Table S4. Estimated expansion times for Golden eagle populations. Times were estimated using the online spreadsheet tool of Schenekar & Weiss (). Generation time (u) was assumed to be 12.5 years, the mutation rate was set to range from 4.54% (min) to 12.54% (max). The same mutation range was used for the Bayesian Skyline estimations. Fennoscandia showed significant deviation from an expansion event; therefore, no expansion time was calculated.</note>
<note type="funding">Austrian Research Promotion Agency</note>
<note type="funding">FEMTech</note>
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