Acquired phototrophy in aquatic protists

dc.contributor.author Stoecker, Diane K.
dc.contributor.author Johnson, Matthew D.
dc.contributor.author de Vargas, Colomban
dc.contributor.author Not, Fabrice
dc.date.accessioned 2011-05-04T13:51:09Z
dc.date.available 2011-05-04T13:51:09Z
dc.date.issued 2009-11-24
dc.description Author Posting. © Inter-Research, 2009. This article is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Aquatic Microbial Ecology 57 (2009): 279-310, doi:10.3354/ame01340. en_US
dc.description.abstract Acquisition of phototrophy is widely distributed in the eukaryotic tree of life and can involve algal endosymbiosis or plastid retention from green or red origins. Species with acquired phototrophy are important components of diversity in aquatic ecosystems, but there are major differences in host and algal taxa involved and in niches of protists with acquired phototrophy in marine and freshwater ecosystems. Organisms that carry out acquired phototrophy are usually mixotrophs, but the degree to which they depend on phototrophy is variable. Evidence suggests that ‘excess carbon’ provided by acquired phototrophy has been important in supporting major evolutionary innovations that are crucial to the current ecological roles of these protists in aquatic ecosystems. Acquired phototrophy occurs primarily among radiolaria, foraminifera, ciliates and dinoflagellates, but is most ecologically important among the first three. Acquired phototrophy in foraminifera and radiolaria is crucial to their contributions to carbonate, silicate, strontium, and carbon flux in subtropical and tropical oceans. Planktonic ciliates with algal kleptoplastids are important in marine and fresh waters, whereas ciliates with green algal endosymbionts are mostly important in freshwaters. The phototrophic ciliate Myrionecta rubra can be a major primary producer in coastal ecosystems. Our knowledge of how acquired phototrophy influences trophic dynamics and biogeochemical cycles is rudimentary; we need to go beyond traditional concepts of ‘plant’ and ‘animal’ functions to progress in our understanding of aquatic microbial ecology. This is a rich area for exploration using a combination of classical and molecular techniques, laboratory and field research, and physiological and ecosystem modeling. en_US
dc.description.sponsorship F.N. and C.dV were supported by a SAD grant SYMFORAD from the Région Bretagne (France) and the BioMarKs project funded by the European ERA-net program BiodivERsA. en_US
dc.format.mimetype application/pdf
dc.identifier.citation Aquatic Microbial Ecology 57 (2009): 279-310 en_US
dc.identifier.doi 10.3354/ame01340
dc.identifier.uri https://hdl.handle.net/1912/4538
dc.language.iso en en_US
dc.publisher Inter-Research en_US
dc.relation.uri https://doi.org/10.3354/ame01340
dc.subject Mixotrophy en_US
dc.subject Radiolaria en_US
dc.subject Foraminifera en_US
dc.subject Ciliates en_US
dc.subject Dinoflagellates en_US
dc.subject Kleptoplastidy en_US
dc.subject Karyoklepty en_US
dc.subject Endosymbiosis en_US
dc.subject Myrionecta rubra en_US
dc.title Acquired phototrophy in aquatic protists en_US
dc.type Article en_US
dspace.entity.type Publication
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relation.isAuthorOfPublication.latestForDiscovery 38c83ac3-7a98-4d34-ba4d-f39584c7d93c
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