Did biogeographical processes shape the monogenean community of butterflyfishes in the tropical Indo-west Pacific region?
Identifieur interne : 000E35 ( PubMed/Checkpoint ); précédent : 000E34; suivant : 000E36Did biogeographical processes shape the monogenean community of butterflyfishes in the tropical Indo-west Pacific region?
Auteurs : M. Reverter [Polynésie française] ; T H Cribb [Australie] ; S C Cutmore [Australie] ; R A Bray [Royaume-Uni] ; V. Parravicini [Polynésie française] ; P. Sasal [Polynésie française]Source :
- International journal for parasitology [ 1879-0135 ] ; 2017.
Abstract
Geographical distribution of parasite species can provide insights into the evolution and diversity of parasitic communities. Biogeography of marine parasites is poorly known, especially because it requires an understanding of host-parasite interactions, information that is rare, especially over large spatial scales. Here, we have studied the biogeographical patterns of dactylogyrid parasites of chaetodontids, one of the most well-studied fish families, in the tropical Indo-west Pacific region. Dactylogyrid parasites were collected from gills of 34 butterflyfish species (n=560) at nine localities within an approximate area of 62millionkm(2). Thirteen dactylogyrid species were identified, with richness ranging from 6 to 12 species at individual localities. Most dactylogyrid communities were dominated by Haliotrema angelopterum or Haliotrema aurigae, for which relative abundance was negatively correlated (ρ=-0.59). Parasite richness and diversity were highest in French Polynesia and the Great Barrier Reef (Australia) and lowest in Palau. Three biogeographic regions were identified based on dactylogyrid dissimilarities: French Polynesia, characterised by the dominance of H. angelopterum, the western Pacific region dominated by H. aurigae, and Ningaloo Reef (Australia), dominated by Euryhaliotrema berenguelae. Structure of host assemblages was the main factor explaining the dissimilarity (turnover and nestedness components of the Bray-Curtis dissimilarity and overall Bray-Curtis dissimilarity) of parasite communities between localities, while environment was only significant in the turnover of parasite communities and overall dissimilarity. Spatial structure of localities explained only 10% of the turnover of parasite communities. The interaction of the three factors (host assemblages, environment and spatial structure), however, explained the highest amounts of variance of the dactylogyrid communities, indicating a strong colinearity between the factors. Our findings show that spatial arrangement of chaetodontid dactylogyrids in the tropical Indo-west Pacific is primarily characterised by the turnover of the main Haliotrema spp., which is mainly explained by the structure of host assemblages.
DOI: 10.1016/j.ijpara.2017.01.006
PubMed: 28322846
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Reverter</name><affiliation wicri:level="1"><nlm:affiliation>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea, French Polynesia. Electronic address: mirireverter@gmail.com.</nlm:affiliation><country xml:lang="fr">Polynésie française</country><wicri:regionArea>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea</wicri:regionArea><wicri:noRegion>98729 Moorea</wicri:noRegion></affiliation></author><author><name sortKey="Cribb, T H" sort="Cribb, T H" uniqKey="Cribb T" first="T H" last="Cribb">T H Cribb</name><affiliation wicri:level="1"><nlm:affiliation>The University of Queensland, School of Biological Sciences, Brisbane, Queensland 4072, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>The University of Queensland, School of Biological Sciences, Brisbane, Queensland 4072</wicri:regionArea><wicri:noRegion>Queensland 4072</wicri:noRegion></affiliation></author><author><name sortKey="Cutmore, S C" sort="Cutmore, S C" uniqKey="Cutmore S" first="S C" last="Cutmore">S C Cutmore</name><affiliation wicri:level="1"><nlm:affiliation>The University of Queensland, School of Biological Sciences, Brisbane, Queensland 4072, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>The University of Queensland, School of Biological Sciences, Brisbane, Queensland 4072</wicri:regionArea><wicri:noRegion>Queensland 4072</wicri:noRegion></affiliation></author><author><name sortKey="Bray, R A" sort="Bray, R A" uniqKey="Bray R" first="R A" last="Bray">R A Bray</name><affiliation wicri:level="1"><nlm:affiliation>Department of Life Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK.</nlm:affiliation><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Life Sciences, Natural History Museum, Cromwell Road, London SW7 5BD</wicri:regionArea><wicri:noRegion>London SW7 5BD</wicri:noRegion></affiliation></author><author><name sortKey="Parravicini, V" sort="Parravicini, V" uniqKey="Parravicini V" first="V" last="Parravicini">V. Parravicini</name><affiliation wicri:level="1"><nlm:affiliation>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea, French Polynesia.</nlm:affiliation><country xml:lang="fr">Polynésie française</country><wicri:regionArea>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea</wicri:regionArea><wicri:noRegion>98729 Moorea</wicri:noRegion></affiliation></author><author><name sortKey="Sasal, P" sort="Sasal, P" uniqKey="Sasal P" first="P" last="Sasal">P. Sasal</name><affiliation wicri:level="1"><nlm:affiliation>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea, French Polynesia.</nlm:affiliation><country xml:lang="fr">Polynésie française</country><wicri:regionArea>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea</wicri:regionArea><wicri:noRegion>98729 Moorea</wicri:noRegion></affiliation></author></analytic><series><title level="j">International journal for parasitology</title><idno type="eISSN">1879-0135</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Geographical distribution of parasite species can provide insights into the evolution and diversity of parasitic communities. Biogeography of marine parasites is poorly known, especially because it requires an understanding of host-parasite interactions, information that is rare, especially over large spatial scales. Here, we have studied the biogeographical patterns of dactylogyrid parasites of chaetodontids, one of the most well-studied fish families, in the tropical Indo-west Pacific region. Dactylogyrid parasites were collected from gills of 34 butterflyfish species (n=560) at nine localities within an approximate area of 62millionkm(2). Thirteen dactylogyrid species were identified, with richness ranging from 6 to 12 species at individual localities. Most dactylogyrid communities were dominated by Haliotrema angelopterum or Haliotrema aurigae, for which relative abundance was negatively correlated (ρ=-0.59). Parasite richness and diversity were highest in French Polynesia and the Great Barrier Reef (Australia) and lowest in Palau. Three biogeographic regions were identified based on dactylogyrid dissimilarities: French Polynesia, characterised by the dominance of H. angelopterum, the western Pacific region dominated by H. aurigae, and Ningaloo Reef (Australia), dominated by Euryhaliotrema berenguelae. Structure of host assemblages was the main factor explaining the dissimilarity (turnover and nestedness components of the Bray-Curtis dissimilarity and overall Bray-Curtis dissimilarity) of parasite communities between localities, while environment was only significant in the turnover of parasite communities and overall dissimilarity. Spatial structure of localities explained only 10% of the turnover of parasite communities. The interaction of the three factors (host assemblages, environment and spatial structure), however, explained the highest amounts of variance of the dactylogyrid communities, indicating a strong colinearity between the factors. Our findings show that spatial arrangement of chaetodontid dactylogyrids in the tropical Indo-west Pacific is primarily characterised by the turnover of the main Haliotrema spp., which is mainly explained by the structure of host assemblages.</div></front></TEI><pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">28322846</PMID><DateCreated><Year>2017</Year><Month>03</Month><Day>21</Day></DateCreated><DateRevised><Year>2017</Year><Month>06</Month><Day>18</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1879-0135</ISSN><JournalIssue CitedMedium="Internet"><Volume>47</Volume><Issue>8</Issue><PubDate><Year>2017</Year><Month>Jul</Month></PubDate></JournalIssue><Title>International journal for parasitology</Title><ISOAbbreviation>Int. J. Parasitol.</ISOAbbreviation></Journal><ArticleTitle>Did biogeographical processes shape the monogenean community of butterflyfishes in the tropical Indo-west Pacific region?</ArticleTitle><Pagination><MedlinePgn>447-455</MedlinePgn></Pagination><ELocationID EIdType="pii" ValidYN="Y">S0020-7519(17)30081-4</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ijpara.2017.01.006</ELocationID><Abstract><AbstractText>Geographical distribution of parasite species can provide insights into the evolution and diversity of parasitic communities. Biogeography of marine parasites is poorly known, especially because it requires an understanding of host-parasite interactions, information that is rare, especially over large spatial scales. Here, we have studied the biogeographical patterns of dactylogyrid parasites of chaetodontids, one of the most well-studied fish families, in the tropical Indo-west Pacific region. Dactylogyrid parasites were collected from gills of 34 butterflyfish species (n=560) at nine localities within an approximate area of 62millionkm(2). Thirteen dactylogyrid species were identified, with richness ranging from 6 to 12 species at individual localities. Most dactylogyrid communities were dominated by Haliotrema angelopterum or Haliotrema aurigae, for which relative abundance was negatively correlated (ρ=-0.59). Parasite richness and diversity were highest in French Polynesia and the Great Barrier Reef (Australia) and lowest in Palau. Three biogeographic regions were identified based on dactylogyrid dissimilarities: French Polynesia, characterised by the dominance of H. angelopterum, the western Pacific region dominated by H. aurigae, and Ningaloo Reef (Australia), dominated by Euryhaliotrema berenguelae. Structure of host assemblages was the main factor explaining the dissimilarity (turnover and nestedness components of the Bray-Curtis dissimilarity and overall Bray-Curtis dissimilarity) of parasite communities between localities, while environment was only significant in the turnover of parasite communities and overall dissimilarity. Spatial structure of localities explained only 10% of the turnover of parasite communities. The interaction of the three factors (host assemblages, environment and spatial structure), however, explained the highest amounts of variance of the dactylogyrid communities, indicating a strong colinearity between the factors. Our findings show that spatial arrangement of chaetodontid dactylogyrids in the tropical Indo-west Pacific is primarily characterised by the turnover of the main Haliotrema spp., which is mainly explained by the structure of host assemblages.</AbstractText><CopyrightInformation>Copyright © 2017 Australian Society for Parasitology. Published by Elsevier Ltd. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Reverter</LastName><ForeName>M</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea, French Polynesia. Electronic address: mirireverter@gmail.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cribb</LastName><ForeName>T H</ForeName><Initials>TH</Initials><AffiliationInfo><Affiliation>The University of Queensland, School of Biological Sciences, Brisbane, Queensland 4072, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cutmore</LastName><ForeName>S C</ForeName><Initials>SC</Initials><AffiliationInfo><Affiliation>The University of Queensland, School of Biological Sciences, Brisbane, Queensland 4072, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bray</LastName><ForeName>R A</ForeName><Initials>RA</Initials><AffiliationInfo><Affiliation>Department of Life Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Parravicini</LastName><ForeName>V</ForeName><Initials>V</Initials><AffiliationInfo><Affiliation>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea, French Polynesia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sasal</LastName><ForeName>P</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Centre des Recherches Insulaires et Observatoire de l'Environnement (CRIOBE), USR3278-EPHE/CNRS/UPVD/PSL, University of Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France; Laboratoire d'Excellence "CORAIL", 98729 Moorea, French Polynesia.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2017</Year><Month>03</Month><Day>18</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Int J Parasitol</MedlineTA><NlmUniqueID>0314024</NlmUniqueID><ISSNLinking>0020-7519</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Butterflyfish</Keyword><Keyword MajorTopicYN="N">Community nestedness</Keyword><Keyword MajorTopicYN="N">Community turnover</Keyword><Keyword MajorTopicYN="N">Dactylogyrids</Keyword><Keyword MajorTopicYN="N">Ectoparasites</Keyword><Keyword MajorTopicYN="N">Host specificity</Keyword><Keyword MajorTopicYN="N">Indo-Pacific</Keyword><Keyword MajorTopicYN="N">Parasite biogeography</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year><Month>11</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2017</Year><Month>01</Month><Day>20</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2017</Year><Month>01</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>3</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>3</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>3</Month><Day>22</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28322846</ArticleId><ArticleId IdType="pii">S0020-7519(17)30081-4</ArticleId><ArticleId IdType="doi">10.1016/j.ijpara.2017.01.006</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Australie</li><li>Polynésie française</li><li>Royaume-Uni</li></country></list><tree><country name="Polynésie française"><noRegion><name sortKey="Reverter, M" sort="Reverter, M" uniqKey="Reverter M" first="M" last="Reverter">M. Reverter</name></noRegion><name sortKey="Parravicini, V" sort="Parravicini, V" uniqKey="Parravicini V" first="V" last="Parravicini">V. Parravicini</name><name sortKey="Sasal, P" sort="Sasal, P" uniqKey="Sasal P" first="P" last="Sasal">P. Sasal</name></country><country name="Australie"><noRegion><name sortKey="Cribb, T H" sort="Cribb, T H" uniqKey="Cribb T" first="T H" last="Cribb">T H Cribb</name></noRegion><name sortKey="Cutmore, S C" sort="Cutmore, S C" uniqKey="Cutmore S" first="S C" last="Cutmore">S C Cutmore</name></country><country name="Royaume-Uni"><noRegion><name sortKey="Bray, R A" sort="Bray, R A" uniqKey="Bray R" first="R A" last="Bray">R A Bray</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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