The ecological distribution and comparative photobiology of symbiotic dinoflagellates from reef corals in Belize: Potential implications for coral bleaching

By Mark E. Warner, Todd C. LaJeunesse, Jennifer D. Robison, Rebecca M. Thur. 2006

193 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/76228dddd081f4767fbec40fcdcef4fc04dc768f

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Citations in the corpus

Understanding diversity in coral-algal symbiosis: a cluster-based approach to interpreting fine-scale genetic variation in the genus Symbiodinium (2009, background): “Based on reports to date, the Caribbean coral Porites astreoides is capable of hosting 11 Symbiodinium ITS-2 types: A1.1, A3, A4, A4a, A14, B1, C1, C1a, C1a-i, C3, and C80 (LaJeunesse 2002; Banaszak et al. 2006; Santos and LaJeunesse 2006; Thornhill et al. 2006; Warner et al. 2006; LaJeunesse et a”
Multiple symbiotic partnerships are common in scleractinian corals, but not in octocorals: Comment on Goulet (2006) (2007, unknown): “…studies (Banaszak et al. 2006, Berkelmans & Van Oppen 2006, Garren et al. 2006, Rotjan et al. 2006, Thornhill et al. 2006b, Ulstrup et al. 2006, Warner et al. 2006, Apprill & Gates 2007), this literature is critical to a metaanalysis of coral flexibility, because these studies involve either…”
Differential effects of ocean acidification on growth and photosynthesis among phylotypes of Symbiodinium (Dinophyceae) (2011, background): “phylotypes (symbiont generalists), whereas other coral species will only ever form a symbiosis with specific phylotypes (symbiont specialists) (Baker 2003; Warner et al. 2006).”
Consensus thermotolerance ranking for 110 Symbiodinium phylotypes: an exemplar utilization of a novel iterative partial‐rank aggregation tool with broad application potential (2017, background): “Commonly cited phylotypes at the extremes of Symbiodinium thermotolerance include thermosensitive C7 and C3 (Warner et al. 2006; Jones et al. 2008; DeSalvo et al. 2010; Silverstein et al. 2011; Wang et al. 2012; Kemp et al. 2014; Keshavmurthy et al. 2014) and thermotolerant D1 and D1-4 (Thornhill…”
Juvenile corals can acquire more carbon from high-performance algal symbionts (2009, background): “Capacity for photoacclimation and tolerance to high irradiance stress has also been linked to the genetic type of Symbiodinium spp., both in culture and within multiple coral host species (Robison and Warner 2006; Warner et al. 2006).”
Chlorophyll Fluorescence in Reef Building Corals (2010, background): “In many cases, photoinactivation is initially detected as a significant drop in F v /F m as well as effective quantum yield, and an initial loss in the return to dark acclimated F v /F m values recorded prior to the application of the stressor, and in some cases these patterns are directly attributa”
Assessing the ‘deep reef refugia’ hypothesis: focus on Caribbean reefs (2010, background): “‘Depth-generalist’ coral species can either harbor a single symbiont over their entire range or show a cladal or subcladal shift of symbionts with depth (e.g., Rowan and Knowlton 1995; Warner et al. 2006; Sampayo et al. 2007; Frade et al. 2008).”
Bleaching Resistance and the Role of Algal Endosymbionts (2009, background): “Montastraea faveolata B1, C7 In hospite C7 loses capacity for diel recovery of photoinhibition earlier than B1 during short-term elevated temperature stress Warner et al. 2006 ”
Host population genetic structure and zooxanthellae diversity of two reef-building coral species along the Florida Reef Tract and wider Caribbean (2010, background): “The Florida Keys present a homogenous population that is distinct from other Caribbean populations (Fig.”
Photobiology of Symbiodinium revisited: bio-physical and bio-optical signatures (2009, background): “…zooxanthellae type within the assemblage (Berkelmans and van Oppen 2006), which may yield discrete patterns of zonation for Symbiodinium assemblages with depth (Iglesias-Prieto et al. 2004; Warner et al. 2006) and across broad geographic scales within a single reef complex (Garren et al. 2006).”