History of the invasive African olive tree in Australia and Hawaii: evidence for sequential bottlenecks and hybridization with the Mediterranean olive.
Identifieur interne : 003501 ( PubMed/Checkpoint ); précédent : 003500; suivant : 003502History of the invasive African olive tree in Australia and Hawaii: evidence for sequential bottlenecks and hybridization with the Mediterranean olive.
Auteurs : Guillaume Besnard [France] ; Jérémy Dupuy [France] ; Maximilien Larter [France] ; Peter Cuneo [Australie] ; David Cooke [Australie] ; Lounes Chikhi [Portugal]Source :
- Evolutionary applications [ 1752-4571 ] ; 2014.
Abstract
Humans have introduced plants and animals into new continents and islands with negative effects on local species. This has been the case of the olive that was introduced in Australia, New Zealand and Pacific islands where it became invasive. Two subspecies were introduced in Australia, and each successfully invaded a specific area: the African olive in New South Wales (NSW) and the Mediterranean olive in South Australia. Here, we examine their origins and spread and analyse a large sample of native and invasive accessions with chloroplast and nuclear microsatellites. African olive populations from the invaded range exhibit two South African chlorotypes hence supporting an introduction from South Africa, while populations from South Australia exhibit chlorotypes of Mediterranean cultivars. Congruently, nuclear markers support the occurrence of two lineages in Australia but demonstrate that admixture took place, attesting that they hybridized early after introduction. Furthermore, using an approximate Bayesian computation framework, we found strong support for the serial introduction of the African olive from South Africa to NSW and then from NSW to Hawaii. The taxon experienced successive bottlenecks that did not preclude invasion, meaning that rapid decisions need to be taken to avoid naturalization where it has not established a large population yet.
DOI: 10.1111/eva.12110
PubMed: 24567742
Affiliations:
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pubmed:24567742Le document en format XML
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Instituto Gulbenkian de Ciência Oreiras, Portugal.</nlm:affiliation><country xml:lang="fr">Portugal</country><wicri:regionArea>Laboratoire Evolution & Diversité Biologique, CNRS, UPS, ENFA, UMR 5174 Toulouse, France ; Instituto Gulbenkian de Ciência Oreiras</wicri:regionArea><wicri:noRegion>France ; Instituto Gulbenkian de Ciência Oreiras</wicri:noRegion></affiliation></author></analytic><series><title level="j">Evolutionary applications</title><idno type="ISSN">1752-4571</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Humans have introduced plants and animals into new continents and islands with negative effects on local species. This has been the case of the olive that was introduced in Australia, New Zealand and Pacific islands where it became invasive. Two subspecies were introduced in Australia, and each successfully invaded a specific area: the African olive in New South Wales (NSW) and the Mediterranean olive in South Australia. Here, we examine their origins and spread and analyse a large sample of native and invasive accessions with chloroplast and nuclear microsatellites. African olive populations from the invaded range exhibit two South African chlorotypes hence supporting an introduction from South Africa, while populations from South Australia exhibit chlorotypes of Mediterranean cultivars. Congruently, nuclear markers support the occurrence of two lineages in Australia but demonstrate that admixture took place, attesting that they hybridized early after introduction. Furthermore, using an approximate Bayesian computation framework, we found strong support for the serial introduction of the African olive from South Africa to NSW and then from NSW to Hawaii. The taxon experienced successive bottlenecks that did not preclude invasion, meaning that rapid decisions need to be taken to avoid naturalization where it has not established a large population yet.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">24567742</PMID><DateCreated><Year>2014</Year><Month>02</Month><Day>25</Day></DateCreated><DateCompleted><Year>2014</Year><Month>02</Month><Day>25</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">1752-4571</ISSN><JournalIssue CitedMedium="Print"><Volume>7</Volume><Issue>2</Issue><PubDate><Year>2014</Year><Month>Feb</Month></PubDate></JournalIssue><Title>Evolutionary applications</Title><ISOAbbreviation>Evol Appl</ISOAbbreviation></Journal><ArticleTitle>History of the invasive African olive tree in Australia and Hawaii: evidence for sequential bottlenecks and hybridization with the Mediterranean olive.</ArticleTitle><Pagination><MedlinePgn>195-211</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/eva.12110</ELocationID><Abstract><AbstractText>Humans have introduced plants and animals into new continents and islands with negative effects on local species. This has been the case of the olive that was introduced in Australia, New Zealand and Pacific islands where it became invasive. Two subspecies were introduced in Australia, and each successfully invaded a specific area: the African olive in New South Wales (NSW) and the Mediterranean olive in South Australia. Here, we examine their origins and spread and analyse a large sample of native and invasive accessions with chloroplast and nuclear microsatellites. African olive populations from the invaded range exhibit two South African chlorotypes hence supporting an introduction from South Africa, while populations from South Australia exhibit chlorotypes of Mediterranean cultivars. Congruently, nuclear markers support the occurrence of two lineages in Australia but demonstrate that admixture took place, attesting that they hybridized early after introduction. Furthermore, using an approximate Bayesian computation framework, we found strong support for the serial introduction of the African olive from South Africa to NSW and then from NSW to Hawaii. The taxon experienced successive bottlenecks that did not preclude invasion, meaning that rapid decisions need to be taken to avoid naturalization where it has not established a large population yet.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Besnard</LastName><ForeName>Guillaume</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Laboratoire Evolution & Diversité Biologique, CNRS, UPS, ENFA, UMR 5174 Toulouse, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dupuy</LastName><ForeName>Jérémy</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Laboratoire Evolution & Diversité Biologique, CNRS, UPS, ENFA, UMR 5174 Toulouse, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Larter</LastName><ForeName>Maximilien</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>INRA, UMR 1202 BIOGECO, Université de Bordeaux Talence, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cuneo</LastName><ForeName>Peter</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>The Australian Botanic Garden, Mount Annan, Royal Botanic Gardens and Domain Trust Mount Annan, NSW, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cooke</LastName><ForeName>David</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Department of Primary Industries and Resources PIRSA, Biosecurity SA Adelaide, SA, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chikhi</LastName><ForeName>Lounes</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Laboratoire Evolution & Diversité Biologique, CNRS, UPS, ENFA, UMR 5174 Toulouse, France ; Instituto Gulbenkian de Ciência Oreiras, Portugal.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2013</Year><Month>11</Month><Day>28</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Evol Appl</MedlineTA><NlmUniqueID>101461828</NlmUniqueID><ISSNLinking>1752-4571</ISSNLinking></MedlineJournalInfo><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Mol Ecol. 2000 Aug;9(8):1171-3</RefSource><PMID Version="1">10964237</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Genetics. 2000 Jun;155(2):945-59</RefSource><PMID Version="1">10835412</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>BMC Bioinformatics. 2010 Jul 28;11:401</RefSource><PMID Version="1">20667077</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Mol Ecol. 2011 Nov;20(22):4654-70</RefSource><PMID Version="1">22004292</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Ecol Lett. 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