2005
DOI: 10.3354/ame040133
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Feeding by phototrophic red-tide dinoflagellates: five species newly revealed and six species previously known to be mixotrophic

Abstract: We report here for the first time that 5 red-tide dinoflagellates (Gymnodinium catenatum, G. impudicum, Lingulodinium polyedrum, Prorocentrum donghaiense, and P. triestinum) which had been previously thought to be exclusively autotrophic dinoflagellates are mixotrophic species. We investigated the feeding behaviors, the kinds of prey species that 11 mixotrophic red-tide dinoflagellates (Akashiwo sanguinea, Alexandrium tamarense, G. catenatum, G. impudicum, Heterocapsa triquetra, L. polyedrum, P. donghaiense, … Show more

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Cited by 229 publications
(216 citation statements)
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“…Given the frequent occurrence of HABs, processes such as algal/bacterial symbiosis (15), delivery from external sources (e.g., benthic fluxes, terrestrial run-off) (22), regeneration from microbial processes, and/or vitamin assimilation via phagotrophy must be crucial processes for maintaining vitamin replete conditions for HABs. Although dinoflagellates are well known phagotrophs (58,59), the stability and subsequent bioavailability of large, complex macromolecules such as vitamins following the digestion of algal prey is unknown.…”
Section: Discussionmentioning
confidence: 99%
“…Given the frequent occurrence of HABs, processes such as algal/bacterial symbiosis (15), delivery from external sources (e.g., benthic fluxes, terrestrial run-off) (22), regeneration from microbial processes, and/or vitamin assimilation via phagotrophy must be crucial processes for maintaining vitamin replete conditions for HABs. Although dinoflagellates are well known phagotrophs (58,59), the stability and subsequent bioavailability of large, complex macromolecules such as vitamins following the digestion of algal prey is unknown.…”
Section: Discussionmentioning
confidence: 99%
“…phagotrophic phototrophs) (Schnepf and Elbrachter 1992;Jeong et al 2005). Nearly all organelle retaining dinoflagellate species sequester their plastids from free-living cryptophyte algae (Larsen 1988;Fields and Rhodes 1991;Horiguchi and Pienaar 1992;Skovgaard 1998;Park et al 2006;Koike and Takishita 2008;Garcia-Cuetos et al 2009, 2010.…”
Section: Organelle-retaining Dinoflagellatesmentioning
confidence: 99%
“…So why are dinoflagellates so prone to novel plastid acquisitions? About half of all dinoflagellate species are heterotrophic or parasitic, and most of the photosynthetic species are mixotrophic (Schnepf and Elbrachter 1992;Jeong et al 2005). Many dinoflagellates that lack stable plastids, practice organelle retention and temporarily enslave algal plastids for photosynthesis (Skovgaard 1998;Jakobsen et al 2000;Stoecker et al 2009).…”
Section: From Phagotrophy To Phototrophy: the Evolution Of Acphmentioning
confidence: 99%
“…A number of allelochemically active microalgae, including species of Alexandrium and Fragilidium, have been shown to be mixotrophic (Jacobson and Anderson, 1986;Tillmann, 1998;Jeong et al, 2005;Stoecker et al, 2006;Yoo et al, 2009;Sheng et al, 2010;Blossom et al, 2012) and it has been speculated that allelochemicals can be deployed for predation. In the present experiments, however phagotrophic uptake of Rhodomonas by Alexandrium was not observed.…”
Section: Lytic Activitymentioning
confidence: 99%