Coral feeding on microalgae assessed with molecular trophic markers
Herbivory in corals, especially for symbiotic species, remains controversial. To investigate the capacity of scleractinian and soft corals to capture microalgae, we conducted controlled laboratory experiments offering five algal species: the cryptophyte Rhodomonas marina, the haptophytes Isochrysis...
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Veröffentlicht in: | Molecular ecology 2014-08, Vol.23 (15), p.3870-3876 |
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description | Herbivory in corals, especially for symbiotic species, remains controversial. To investigate the capacity of scleractinian and soft corals to capture microalgae, we conducted controlled laboratory experiments offering five algal species: the cryptophyte Rhodomonas marina, the haptophytes Isochrysis galbana and Phaeocystis globosa, and the diatoms Conticribra weissflogii and Thalassiosira pseudonana. Coral species included the symbiotic soft corals Heteroxenia fuscescens and Sinularia flexibilis, the asymbiotic scleractinian coral Tubastrea coccinea, and the symbiotic scleractinian corals Stylophora pistillata, Pavona cactus and Oculina arbuscula. Herbivory was assessed by end‐point PCR amplification of algae‐specific 18S rRNA gene fragments purified from coral tissue genomic DNA extracts. The ability to capture microalgae varied with coral and algal species and could not be explained by prey size or taxonomy. Herbivory was not detected in S. flexibilis and S. pistillata. P. globosa was the only algal prey that was never captured by any coral. Although predation defence mechanisms have been shown for Phaeocystis spp. against many potential predators, this study is the first to suggest this for corals. This study provides new insights into herbivory in symbiotic corals and suggests that corals may be selective herbivorous feeders. |
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To investigate the capacity of scleractinian and soft corals to capture microalgae, we conducted controlled laboratory experiments offering five algal species: the cryptophyte Rhodomonas marina, the haptophytes Isochrysis galbana and Phaeocystis globosa, and the diatoms Conticribra weissflogii and Thalassiosira pseudonana. Coral species included the symbiotic soft corals Heteroxenia fuscescens and Sinularia flexibilis, the asymbiotic scleractinian coral Tubastrea coccinea, and the symbiotic scleractinian corals Stylophora pistillata, Pavona cactus and Oculina arbuscula. Herbivory was assessed by end‐point PCR amplification of algae‐specific 18S rRNA gene fragments purified from coral tissue genomic DNA extracts. The ability to capture microalgae varied with coral and algal species and could not be explained by prey size or taxonomy. Herbivory was not detected in S. flexibilis and S. pistillata. P. globosa was the only algal prey that was never captured by any coral. Although predation defence mechanisms have been shown for Phaeocystis spp. against many potential predators, this study is the first to suggest this for corals. This study provides new insights into herbivory in symbiotic corals and suggests that corals may be selective herbivorous feeders.</description><identifier>ISSN: 0962-1083</identifier><identifier>EISSN: 1365-294X</identifier><identifier>DOI: 10.1111/mec.12486</identifier><identifier>PMID: 24112432</identifier><language>eng</language><publisher>England: Blackwell Science</publisher><subject>Algae ; Animals ; Anthozoa - physiology ; cacti and succulents ; coral feeding ; Coral reefs ; corals ; defense mechanisms ; DNA ; Food Chain ; genes ; Herbivores ; Herbivory ; heterotrophy ; Heteroxenia fuscescens ; Isochrysis galbana ; laboratory experimentation ; Marine biology ; Marine ecology ; microalgae ; Microalgae - genetics ; Oculina arbuscula ; Pavona cactus ; PCR ; Phaeocystis ; Phaeocystis globosa ; phytoplankton ; polymerase chain reaction ; predation ; predators ; Rhodomonas ; ribosomal RNA ; RNA, Ribosomal, 18S - analysis ; Scleractinia ; Sequence Analysis, DNA ; Sinularia ; Sinularia flexibilis ; specific primers ; Stylophora pistillata ; Symbiosis ; taxonomy ; Thalassiosira ; Thalassiosira pseudonana ; Tubastrea coccinea</subject><ispartof>Molecular ecology, 2014-08, Vol.23 (15), p.3870-3876</ispartof><rights>2013 John Wiley & Sons Ltd</rights><rights>2013 John Wiley & Sons Ltd.</rights><rights>Copyright © 2014 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5076-afc4973c8e5b844e66e02abf5e4ca8c7c92ff453daa6fc90a8af755d1b889ea33</citedby><cites>FETCH-LOGICAL-c5076-afc4973c8e5b844e66e02abf5e4ca8c7c92ff453daa6fc90a8af755d1b889ea33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fmec.12486$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fmec.12486$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24112432$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leal, Miguel C</creatorcontrib><creatorcontrib>Ferrier‐Pagès, Christine</creatorcontrib><creatorcontrib>Calado, Ricardo</creatorcontrib><creatorcontrib>Thompson, Megan E</creatorcontrib><creatorcontrib>Frischer, Marc E</creatorcontrib><creatorcontrib>Nejstgaard, Jens C</creatorcontrib><title>Coral feeding on microalgae assessed with molecular trophic markers</title><title>Molecular ecology</title><addtitle>Mol Ecol</addtitle><description>Herbivory in corals, especially for symbiotic species, remains controversial. To investigate the capacity of scleractinian and soft corals to capture microalgae, we conducted controlled laboratory experiments offering five algal species: the cryptophyte Rhodomonas marina, the haptophytes Isochrysis galbana and Phaeocystis globosa, and the diatoms Conticribra weissflogii and Thalassiosira pseudonana. Coral species included the symbiotic soft corals Heteroxenia fuscescens and Sinularia flexibilis, the asymbiotic scleractinian coral Tubastrea coccinea, and the symbiotic scleractinian corals Stylophora pistillata, Pavona cactus and Oculina arbuscula. Herbivory was assessed by end‐point PCR amplification of algae‐specific 18S rRNA gene fragments purified from coral tissue genomic DNA extracts. The ability to capture microalgae varied with coral and algal species and could not be explained by prey size or taxonomy. Herbivory was not detected in S. flexibilis and S. pistillata. P. globosa was the only algal prey that was never captured by any coral. Although predation defence mechanisms have been shown for Phaeocystis spp. against many potential predators, this study is the first to suggest this for corals. This study provides new insights into herbivory in symbiotic corals and suggests that corals may be selective herbivorous feeders.</description><subject>Algae</subject><subject>Animals</subject><subject>Anthozoa - physiology</subject><subject>cacti and succulents</subject><subject>coral feeding</subject><subject>Coral reefs</subject><subject>corals</subject><subject>defense mechanisms</subject><subject>DNA</subject><subject>Food Chain</subject><subject>genes</subject><subject>Herbivores</subject><subject>Herbivory</subject><subject>heterotrophy</subject><subject>Heteroxenia fuscescens</subject><subject>Isochrysis galbana</subject><subject>laboratory experimentation</subject><subject>Marine biology</subject><subject>Marine ecology</subject><subject>microalgae</subject><subject>Microalgae - genetics</subject><subject>Oculina arbuscula</subject><subject>Pavona cactus</subject><subject>PCR</subject><subject>Phaeocystis</subject><subject>Phaeocystis globosa</subject><subject>phytoplankton</subject><subject>polymerase chain reaction</subject><subject>predation</subject><subject>predators</subject><subject>Rhodomonas</subject><subject>ribosomal RNA</subject><subject>RNA, Ribosomal, 18S - analysis</subject><subject>Scleractinia</subject><subject>Sequence Analysis, DNA</subject><subject>Sinularia</subject><subject>Sinularia flexibilis</subject><subject>specific primers</subject><subject>Stylophora pistillata</subject><subject>Symbiosis</subject><subject>taxonomy</subject><subject>Thalassiosira</subject><subject>Thalassiosira pseudonana</subject><subject>Tubastrea coccinea</subject><issn>0962-1083</issn><issn>1365-294X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0s9rFDEUB_Agit1WD_4DOuBFD9Pm9yTHMtRVqAqudXsL2czLNnVmsyY7tP3vzTptD4JgCOTyeV947wWhVwQfk3JOBnDHhHIln6AZYVLUVPPLp2iGtaQ1wYodoMOcrzEmjArxHB1QTopndIbaNibbVx6gC5t1FTfVEFyKtl9bqGzOUG5X3YTdVTXEHtzY21TtUtxeBVcNNv2ElF-gZ972GV7ev0fo4sPZ9_Zjff51_qk9Pa-dwI2srXdcN8wpECvFOUgJmNqVF8CdVa5xmnrPBeusld5pbJX1jRAdWSmlwTJ2hN5NudsUf42Qd2YI2UHf2w3EMRsiBNcCY67-g3JFNJO8KfTtX_Q6jmlTGtmrhhGB1T7w_aTKcHJO4M02hdL_nSHY7JdgyhLMnyUU-_o-cVwN0D3Kh6kXcDKBm9DD3b-TzOez9iGynipC3sHtY0WZv5ENa4RZfpmbbz_wYr5cXppF8W8m7200dp1CNhcLignf_wGuKWO_AePYqFI</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Leal, Miguel C</creator><creator>Ferrier‐Pagès, Christine</creator><creator>Calado, Ricardo</creator><creator>Thompson, Megan E</creator><creator>Frischer, Marc E</creator><creator>Nejstgaard, Jens C</creator><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7TN</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>201408</creationdate><title>Coral feeding on microalgae assessed with molecular trophic markers</title><author>Leal, Miguel C ; Ferrier‐Pagès, Christine ; Calado, Ricardo ; Thompson, Megan E ; Frischer, Marc E ; Nejstgaard, Jens C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5076-afc4973c8e5b844e66e02abf5e4ca8c7c92ff453daa6fc90a8af755d1b889ea33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Algae</topic><topic>Animals</topic><topic>Anthozoa - physiology</topic><topic>cacti and succulents</topic><topic>coral feeding</topic><topic>Coral reefs</topic><topic>corals</topic><topic>defense mechanisms</topic><topic>DNA</topic><topic>Food Chain</topic><topic>genes</topic><topic>Herbivores</topic><topic>Herbivory</topic><topic>heterotrophy</topic><topic>Heteroxenia fuscescens</topic><topic>Isochrysis galbana</topic><topic>laboratory experimentation</topic><topic>Marine biology</topic><topic>Marine ecology</topic><topic>microalgae</topic><topic>Microalgae - genetics</topic><topic>Oculina arbuscula</topic><topic>Pavona cactus</topic><topic>PCR</topic><topic>Phaeocystis</topic><topic>Phaeocystis globosa</topic><topic>phytoplankton</topic><topic>polymerase chain reaction</topic><topic>predation</topic><topic>predators</topic><topic>Rhodomonas</topic><topic>ribosomal RNA</topic><topic>RNA, Ribosomal, 18S - analysis</topic><topic>Scleractinia</topic><topic>Sequence Analysis, DNA</topic><topic>Sinularia</topic><topic>Sinularia flexibilis</topic><topic>specific primers</topic><topic>Stylophora pistillata</topic><topic>Symbiosis</topic><topic>taxonomy</topic><topic>Thalassiosira</topic><topic>Thalassiosira pseudonana</topic><topic>Tubastrea coccinea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leal, Miguel C</creatorcontrib><creatorcontrib>Ferrier‐Pagès, Christine</creatorcontrib><creatorcontrib>Calado, Ricardo</creatorcontrib><creatorcontrib>Thompson, Megan E</creatorcontrib><creatorcontrib>Frischer, Marc E</creatorcontrib><creatorcontrib>Nejstgaard, Jens C</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Molecular ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leal, Miguel C</au><au>Ferrier‐Pagès, Christine</au><au>Calado, Ricardo</au><au>Thompson, Megan E</au><au>Frischer, Marc E</au><au>Nejstgaard, Jens C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coral feeding on microalgae assessed with molecular trophic markers</atitle><jtitle>Molecular ecology</jtitle><addtitle>Mol Ecol</addtitle><date>2014-08</date><risdate>2014</risdate><volume>23</volume><issue>15</issue><spage>3870</spage><epage>3876</epage><pages>3870-3876</pages><issn>0962-1083</issn><eissn>1365-294X</eissn><abstract>Herbivory in corals, especially for symbiotic species, remains controversial. To investigate the capacity of scleractinian and soft corals to capture microalgae, we conducted controlled laboratory experiments offering five algal species: the cryptophyte Rhodomonas marina, the haptophytes Isochrysis galbana and Phaeocystis globosa, and the diatoms Conticribra weissflogii and Thalassiosira pseudonana. Coral species included the symbiotic soft corals Heteroxenia fuscescens and Sinularia flexibilis, the asymbiotic scleractinian coral Tubastrea coccinea, and the symbiotic scleractinian corals Stylophora pistillata, Pavona cactus and Oculina arbuscula. Herbivory was assessed by end‐point PCR amplification of algae‐specific 18S rRNA gene fragments purified from coral tissue genomic DNA extracts. The ability to capture microalgae varied with coral and algal species and could not be explained by prey size or taxonomy. Herbivory was not detected in S. flexibilis and S. pistillata. P. globosa was the only algal prey that was never captured by any coral. Although predation defence mechanisms have been shown for Phaeocystis spp. against many potential predators, this study is the first to suggest this for corals. This study provides new insights into herbivory in symbiotic corals and suggests that corals may be selective herbivorous feeders.</abstract><cop>England</cop><pub>Blackwell Science</pub><pmid>24112432</pmid><doi>10.1111/mec.12486</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algae Animals Anthozoa - physiology cacti and succulents coral feeding Coral reefs corals defense mechanisms DNA Food Chain genes Herbivores Herbivory heterotrophy Heteroxenia fuscescens Isochrysis galbana laboratory experimentation Marine biology Marine ecology microalgae Microalgae - genetics Oculina arbuscula Pavona cactus PCR Phaeocystis Phaeocystis globosa phytoplankton polymerase chain reaction predation predators Rhodomonas ribosomal RNA RNA, Ribosomal, 18S - analysis Scleractinia Sequence Analysis, DNA Sinularia Sinularia flexibilis specific primers Stylophora pistillata Symbiosis taxonomy Thalassiosira Thalassiosira pseudonana Tubastrea coccinea |
title | Coral feeding on microalgae assessed with molecular trophic markers |
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