Distinct ITS types of Symbiodinium in clade C correlate with cnidarian/dinoflagellate specificity during onset of symbiosis
By M. Rodriguez-Lanetty, D. Krupp, V. Weis. 2004
106 citations recorded by the source corpus.
Subfields: Ecology, Oceanography
View Paper: https://www.semanticscholar.org/paper/944fa60eb9e8ccc486be2a153a2075515f1e142a
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In Ecology
- A. Baker
- O. Hoegh‐Guldberg
- M. Stat
- W. Fitt
- Gregory W. Schmidt
- Todd C. LaJeunesse
- M. Oppen
- D. Thornhill
In Oceanography
- A. Baker
- M. Stat
- W. Fitt
- O. Hoegh‐Guldberg
- Todd C. LaJeunesse
- Gregory W. Schmidt
- M. Oppen
- D. Thornhill
Citations in the corpus
- Multi-year, seasonal genotypic surveys of coral-algal symbioses reveal prevalent stability or post-bleaching reversion (2006, background): “Fitt 1985); (2) molecular compatibility and/ or recognition in new symbiont recruitment (host-specificity/selection) (e.g. Gates et al. 1995; Reynolds et al. 2000; Rodriguez-Lanetty et al. 2004) may restrict the variation of host-symbiont combinations; the five types of Symbiodinium associated with ”
- Long‐standing environmental conditions, geographic isolation and host–symbiont specificity influence the relative ecological dominance and genetic diversification of coral endosymbionts in the genus Symbiodinium (2010, background): “…differences in these ITS sequences delimit ecologically distinct Symbiodinium (operational taxonomic units, or OTUs; e.g. LaJeunesse, 2002; Pochon et al., 2004, 2007; Rodriguez-Lanetty et al., 2004; Thornhill et al., 2006b, 2008; Sampayo et al., 2007, 2008; Frade et al., 2008; Goulet et al., 2008).”
- Alexandrium catenella (Dinophyceae), a toxic ribotype expanding in the NW Mediterranean Sea (2005, background): “The total alignment of the ITS1 and ITS2 regions among different microalgal isolates is usually neglected, since greater variability can be found in the ITS2 region (Orsini et al. 2004; Rodriguez-Lanetty et al. 2004).”
- Assessing the ‘deep reef refugia’ hypothesis: focus on Caribbean reefs (2010, background): “Comparing endosymbiont community composition of parental populations and offspring reveals that, similar to selection of parental habitat, juveniles adopt Symbiodinium types similar to that of the parent (Coffroth et al. 2001; Weis et al. 2001; Rodriguez-Lanetty et al. 2004).”
- One-year survey of a single Micronesian reef reveals extraordinarily rich diversity of Symbiodinium types in soritid foraminifera (2007, background): “…taxonomic, geographic, and/or environmental distribution (LaJeunesse 2002, 2005; Ulstrup and van Oppen 2003; LaJeunesse et al. 2004a, b; Pochon et al. 2004; Rodriguez-Lanetty et al. 2004), considering each of the hundreds of described ITS-2 types as individual species is questionable at this time.”
- High diversity and host specificity observed among symbiotic dinoflagellates in reef coral communities from Hawaii (2004, background): “This symbiont when compared against types C15, Cld, and C31, originating from P. compressa, P. damicornis , and M. capitata respectively, infects with greater success and achieves higher growth rates in Fungia scutaria larvae (Weis et al. 2001; Rodriguez-Lanetty et al. 2004).”
- Novel algal symbiont (Symbiodinium spp.) diversity in reef corals of Western Australia (2011, background): “Scleractinian corals typically associate with Symbiodinium in 4 sub-generic clades, A, B, C, and D (reviewed in Baker 2003), while symbionts in clades F and G are only rarely harbored by stony corals (Rodriguez-Lanetty et al. 2004, LaJeunesse et al. 2010a).”
- Symbiont acquisition strategy drives host–symbiont associations in the southern Great Barrier Reef (2008, background): “In addition, some horizontal strategists can show evidence of speciWcity, as was observed in Fungia scutaria from Hawaii, which acquires its symbionts from the environment but was found to house the specialist Symbiodinium genotype ITS2 C1f (Weis et al. 2001; Rodriguez-Lanetty et al. 2004 ).”
- The relative contribution of dinoflagellate photosynthesis and stored lipids to the survivorship of symbiotic larvae of the reef-building corals (2010, background): “Some aposymbiotic corals have been reported to acquire symbiotic dinoXagellates during the larval stage under experimental conditions (Schwarz et al. 1999; Weis et al. 2001; Rodriguez-Lanetty et al. 2004; Nozawa and Harrison 2005; Baird et al. 2006; Harii et al. 2009).”
- Bleaching Resistance and the Role of Algal Endosymbionts (2009, background): “symbionts inside the host tissues ( Rodriguez-Lanetty et al. 2004, 2006 ).”
- The ecology and phylogeny of cyanobacterial symbionts in sponges (2008, unknown): “corals (Rodriguez-Lanetty et al. 2004), and anemones (BeldaBaillie et al.”
- Ecologically differentiated stress-tolerant endosymbionts in the dinoflagellate genus Symbiodinium (Dinophyceae) Clade D are different species (2014, background): “…have different physiological and ecological attributes, further revealing that they are genetically and functionally distinct entities (LaJeunesse 2002; Rodriguez-Lanetty et al. 2004; Frade et al. 2008; Thornhill et al. 2008; Hennige et al. 2009; Sampayo et al. 2008, 2009), and efforts necessary…”