On the functional significance of molecular variation in Symbiodinium, the symbiotic algae of Cnidaria: photosynthetic response to irradiance

By A. Savage, H. Trapido-Rosenthal, A. E. Douglas. 2002

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View Paper: https://www.semanticscholar.org/paper/ad889767217b0064bca53da2226f0d8f3293bb13

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Citations in the corpus

Photobiology of Symbiodinium revisited: bio-physical and bio-optical signatures (2009, background): “Previous laboratory investigations have confirmed photoadaptation amongst different Symbiodinium types when grown under identical conditions (Chang et al. 1983; Iglesias-Prieto and Trench 1994, 1997; Savage et al. 2002; Rodriguez-Roman and Iglesias-Prieto 2005; Robison and Warner 2006; Suggett et al”
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): “Virtually unstudied, the functional diversity found within various clades of Symbiodinium is potentially high (e.g. Savage et al., 2002; Tchernov et al., 2004; Sampayo et al., 2008; Thornhill et al., 2008) and may include species important to coral communities during times of major climate change.”
Experimental biology of coral reef ecosystems (2004, background): “, 2003), other works on general photosynthetic capabilities have shown less difference between clades (Savage et al., 2002).”
Flexibility and Specificity in Coral-Algal Symbiosis: Diversity, Ecology, and Biogeography of Symbiodinium (2003, unknown): “…2001, Pochon et al. 2001, Savage et al. 2002a, Toller 2001b, Van Oppen et al. 2001, Wilcox 1998), and internal transcribed spacers (ITS 1 and 2) and 5.8S regions (Brown et al. 2000, 2002; Hunter et al. 1997; LaJeunesse 2001, 2002; LaJeunesse et al. 2003; Savage et al. 2002a; Van Oppen et al. 2001).”
Multiple symbiotic partnerships are common in scleractinian corals, but not in octocorals: Comment on Goulet (2006) (2007, background): “Because significant physiological variability exists within clades (Savage et al. 2002, Tchernov et al. 2004), we cannot ignore the potentially critical role this diversity plays in understanding the physiological capacity of reef corals in response to environmental change.”
Adaptive bleaching: a general phenomenon (2004, background): “Although different zooxanthella phylotypes differ physiologically, at least some photosynthetic traits do not correlate directly with characteristics of the phylotype ( Savage et al., 2002b ).”
The ecological distribution and comparative photobiology of symbiotic dinoflagellates from reef corals in Belize: Potential implications for coral bleaching (2006, background): “…of morphological and physiological diversity within this genus, and in general there is no clear correlation between ecological or physiological performance and the generic clades commonly used to identify these algae (Iglesias-Prieto and Trench 1997; Savage et al. 2002; Tchernov et al. 2004).”
Variation in bleaching sensitivity of two coral species across a latitudinal gradient on the Great Barrier Reef: the role of zooxanthellae (2006, result): “Similar results have been found with regard to latitude (Loh et al. 2001, Rodriguez-Lanetty et al. 2001, Savage et al. 2002).”
Distinct ITS types of Symbiodinium in clade C correlate with cnidarian/dinoflagellate specificity during onset of symbiosis (2004, background): “However, recent data have shown that photo-physiological responses of in hospite Symbiodinium do not map directly onto major algal clades (Savage et al. 2002).”
Effect of short‐term exposure to elevated temperatures and light levels on photosynthesis of different host‐symbiont combinations in the Aiptasia pallida/Symbiodinium symbiosis (2005, background): “In Bermuda, A. pallida appears to contain only clade B zooxanthellae (Rowan and Powers 1991; Savage et al. 2002; this article).”
The Adaptive Hypothesis of Bleaching (2004, background): “Some studies using relatively conserved molecular methods have failed to resolve algal taxa that clearly differ functionally in terms of their response to environmental parameters (Kinzie et al. 2001, Savage et al. 2002b).”
Bleaching Resistance and the Role of Algal Endosymbionts (2009, background): “cavernosa, M. franksi, Oculina diffusa, Porites astreoides, Aiptasia pallida, Bartholomea annulata, Condylactis gigantea, Cassiopeia xamachana A, B, C Freshly isolated PI curves are not uniform for all members of one clade and not consistently different between clades Savage et al. 2002b 92 M.J.H.”