Symbiosis between the Zooxanthella Symbiodinium (= Gymnodinium) microadriaticum (Freudenthal) and Four Species of Nudibranchs
The dinoflagellate Symbiodinium (= Gymnodinum) microadriaticum (Freudenthal) occurs in a symbiotic association with the nudibranchs Melibe pilosa, an undescribed Melibe sp., Pteraeolidea ianthina, and Berghia major. The algal symbionts reside in host-derived "carrier" cells associated with...
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Veröffentlicht in: | The Biological bulletin 1984-02, Vol.166 (1), p.110-126 |
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description | The dinoflagellate Symbiodinium (= Gymnodinum) microadriaticum (Freudenthal) occurs in a symbiotic association with the nudibranchs Melibe pilosa, an undescribed Melibe sp., Pteraeolidea ianthina, and Berghia major. The algal symbionts reside in host-derived "carrier" cells associated with the host's digestive gland. Longer survival of starved M. pilosa, P. ianthina, and B. major in constant light than in constant dark indicates that photosynthetically fixed carbon is translocated from symbiont to host. Large lipid deposits, present in the same animal cells that contain zooxanthellae in Melibe sp. and P. ianthina, suggest that lipid or lipid precursors may comprise part of the translocated nutrients in these species. A large proportion of the fecal material in Melibe sp., P. ianthina, and B. major is composed of degenerate algal cells. It is possible that these species obtain part or all of their translocated nutrients by digestion of some of their algal symbionts. An organ that appears to function as the site of zooxanthella digestion is present in the cerata of P. ianthina. Zygotes and larvae of all four nudibranch species are devoid of symbionts, thus each new host generation must be re-infected with S. microadriaticum. Adults of B. major feed on prey that contain symbiotic zooxanthellae while the other three nudibranch species examined do not. These facts suggest that while the historic inception of the symbiosis in B. major was probably secondary, the symbionts being derived from the prey; in M. pilosa, Melibe sp., and P. ianthina the inception may have been primary, the symbionts being obtained by inadvertant ingestion by the host. |
doi_str_mv | 10.2307/1541435 |
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The algal symbionts reside in host-derived "carrier" cells associated with the host's digestive gland. Longer survival of starved M. pilosa, P. ianthina, and B. major in constant light than in constant dark indicates that photosynthetically fixed carbon is translocated from symbiont to host. Large lipid deposits, present in the same animal cells that contain zooxanthellae in Melibe sp. and P. ianthina, suggest that lipid or lipid precursors may comprise part of the translocated nutrients in these species. A large proportion of the fecal material in Melibe sp., P. ianthina, and B. major is composed of degenerate algal cells. It is possible that these species obtain part or all of their translocated nutrients by digestion of some of their algal symbionts. An organ that appears to function as the site of zooxanthella digestion is present in the cerata of P. ianthina. Zygotes and larvae of all four nudibranch species are devoid of symbionts, thus each new host generation must be re-infected with S. microadriaticum. Adults of B. major feed on prey that contain symbiotic zooxanthellae while the other three nudibranch species examined do not. These facts suggest that while the historic inception of the symbiosis in B. major was probably secondary, the symbionts being derived from the prey; in M. pilosa, Melibe sp., and P. ianthina the inception may have been primary, the symbionts being obtained by inadvertant ingestion by the host.</description><identifier>ISSN: 0006-3185</identifier><identifier>EISSN: 1939-8697</identifier><identifier>DOI: 10.2307/1541435</identifier><language>eng</language><publisher>Woods Hole, MA: Marine Biological Laboratory</publisher><subject>Algae ; Animal glands ; Animals ; Biological and medical sciences ; Digestion ; Ecology and Evolution ; Fundamental and applied biological sciences. Psychology ; Larvae ; Lipids ; Marine ; Melibe ; Parasite hosts ; Parasitism and symbiosis ; Plant physiology and development ; Starvation ; Symbiodinium microadriaticum ; Symbionts ; Symbiosis</subject><ispartof>The Biological bulletin, 1984-02, Vol.166 (1), p.110-126</ispartof><rights>Copyright 1984 The Marine Biological Laboratory</rights><rights>1984 INIST-CNRS</rights><rights>In copyright. Digitized with the permission of the rights holder. http://creativecommons.org/licenses/by-nc-sa/3.0</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2938-333ac63ca747fb3ae6a00574d80d978583dadfa44f3ac20ac8a54d91d3ad152a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1541435$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1541435$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,885,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9631647$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kempf, Stephen C.</creatorcontrib><title>Symbiosis between the Zooxanthella Symbiodinium (= Gymnodinium) microadriaticum (Freudenthal) and Four Species of Nudibranchs</title><title>The Biological bulletin</title><description>The dinoflagellate Symbiodinium (= Gymnodinum) microadriaticum (Freudenthal) occurs in a symbiotic association with the nudibranchs Melibe pilosa, an undescribed Melibe sp., Pteraeolidea ianthina, and Berghia major. The algal symbionts reside in host-derived "carrier" cells associated with the host's digestive gland. Longer survival of starved M. pilosa, P. ianthina, and B. major in constant light than in constant dark indicates that photosynthetically fixed carbon is translocated from symbiont to host. Large lipid deposits, present in the same animal cells that contain zooxanthellae in Melibe sp. and P. ianthina, suggest that lipid or lipid precursors may comprise part of the translocated nutrients in these species. A large proportion of the fecal material in Melibe sp., P. ianthina, and B. major is composed of degenerate algal cells. It is possible that these species obtain part or all of their translocated nutrients by digestion of some of their algal symbionts. An organ that appears to function as the site of zooxanthella digestion is present in the cerata of P. ianthina. Zygotes and larvae of all four nudibranch species are devoid of symbionts, thus each new host generation must be re-infected with S. microadriaticum. Adults of B. major feed on prey that contain symbiotic zooxanthellae while the other three nudibranch species examined do not. These facts suggest that while the historic inception of the symbiosis in B. major was probably secondary, the symbionts being derived from the prey; in M. pilosa, Melibe sp., and P. ianthina the inception may have been primary, the symbionts being obtained by inadvertant ingestion by the host.</description><subject>Algae</subject><subject>Animal glands</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Digestion</subject><subject>Ecology and Evolution</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Larvae</subject><subject>Lipids</subject><subject>Marine</subject><subject>Melibe</subject><subject>Parasite hosts</subject><subject>Parasitism and symbiosis</subject><subject>Plant physiology and development</subject><subject>Starvation</subject><subject>Symbiodinium microadriaticum</subject><subject>Symbionts</subject><subject>Symbiosis</subject><issn>0006-3185</issn><issn>1939-8697</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>79B</sourceid><recordid>eNp1kT1P5DAQhi10SOwB4i-4QHAUATt2vgqKE2IBCUEBNDTWrO2wRom9eBJgC_47CbsCXXGVPfbjR-N3CNnj7DgVrDjhmeRSZBtkwitRJWVeFb_IhDGWJ4KX2Rb5jfg8lCzlckI-7pbtzAV0SGe2e7PW025u6WMI7-CHXdMAXSHGede39M8pvVi2fl0e0dbpGMBEB53T4_002t7Y4S00RxS8odPQR3q3sNpZpKGmN71xswhez3GHbNbQoN1dr9vkYXp-f3aZXN9eXJ39vU50WokyEUKAzoWGQhb1TIDNgbGskKZkpirKrBQGTA1S1gOXMtAlZNJU3AgwPEtBbJOrlRdb180xeAdeff3p1UZ03VK9piqA--esGbuMSxXik1pA7JQoclkOroOVaxHDS2-xU61DPQblbehRcZnKPM2qATxcgUNAiNHWahFdOxo5U-Oo1HpUA7m_VgJqaOoxHIffeJULnsviB3vGLsT_2j4BSvGidw</recordid><startdate>19840201</startdate><enddate>19840201</enddate><creator>Kempf, Stephen C.</creator><general>Marine Biological Laboratory</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TN</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>79B</scope></search><sort><creationdate>19840201</creationdate><title>Symbiosis between the Zooxanthella Symbiodinium (= Gymnodinium) microadriaticum (Freudenthal) and Four Species of Nudibranchs</title><author>Kempf, Stephen C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2938-333ac63ca747fb3ae6a00574d80d978583dadfa44f3ac20ac8a54d91d3ad152a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Algae</topic><topic>Animal glands</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Digestion</topic><topic>Ecology and Evolution</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Larvae</topic><topic>Lipids</topic><topic>Marine</topic><topic>Melibe</topic><topic>Parasite hosts</topic><topic>Parasitism and symbiosis</topic><topic>Plant physiology and development</topic><topic>Starvation</topic><topic>Symbiodinium microadriaticum</topic><topic>Symbionts</topic><topic>Symbiosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kempf, Stephen C.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</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><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biodiversity Heritage Library</collection><jtitle>The Biological bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kempf, Stephen C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Symbiosis between the Zooxanthella Symbiodinium (= Gymnodinium) microadriaticum (Freudenthal) and Four Species of Nudibranchs</atitle><jtitle>The Biological bulletin</jtitle><date>1984-02-01</date><risdate>1984</risdate><volume>166</volume><issue>1</issue><spage>110</spage><epage>126</epage><pages>110-126</pages><issn>0006-3185</issn><eissn>1939-8697</eissn><abstract>The dinoflagellate Symbiodinium (= Gymnodinum) microadriaticum (Freudenthal) occurs in a symbiotic association with the nudibranchs Melibe pilosa, an undescribed Melibe sp., Pteraeolidea ianthina, and Berghia major. The algal symbionts reside in host-derived "carrier" cells associated with the host's digestive gland. Longer survival of starved M. pilosa, P. ianthina, and B. major in constant light than in constant dark indicates that photosynthetically fixed carbon is translocated from symbiont to host. Large lipid deposits, present in the same animal cells that contain zooxanthellae in Melibe sp. and P. ianthina, suggest that lipid or lipid precursors may comprise part of the translocated nutrients in these species. A large proportion of the fecal material in Melibe sp., P. ianthina, and B. major is composed of degenerate algal cells. It is possible that these species obtain part or all of their translocated nutrients by digestion of some of their algal symbionts. An organ that appears to function as the site of zooxanthella digestion is present in the cerata of P. ianthina. Zygotes and larvae of all four nudibranch species are devoid of symbionts, thus each new host generation must be re-infected with S. microadriaticum. Adults of B. major feed on prey that contain symbiotic zooxanthellae while the other three nudibranch species examined do not. These facts suggest that while the historic inception of the symbiosis in B. major was probably secondary, the symbionts being derived from the prey; in M. pilosa, Melibe sp., and P. ianthina the inception may have been primary, the symbionts being obtained by inadvertant ingestion by the host.</abstract><cop>Woods Hole, MA</cop><pub>Marine Biological Laboratory</pub><doi>10.2307/1541435</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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source | Jstor Complete Legacy; EZB-FREE-00999 freely available EZB journals |
subjects | Algae Animal glands Animals Biological and medical sciences Digestion Ecology and Evolution Fundamental and applied biological sciences. Psychology Larvae Lipids Marine Melibe Parasite hosts Parasitism and symbiosis Plant physiology and development Starvation Symbiodinium microadriaticum Symbionts Symbiosis |
title | Symbiosis between the Zooxanthella Symbiodinium (= Gymnodinium) microadriaticum (Freudenthal) and Four Species of Nudibranchs |
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