Lipids and stable carbon isotopes in two species of Hawaiian corals, Porites compressa and Montipora verrucosa, following a bleaching event

By A. Grottoli, L. Rodrigues, C. Juárez. 2004

305 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/3fa84815b2bff1d2c3a1cb2939159a90a52f36c6

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Citations in the corpus

Impact of feeding and short-term temperature stress on the content and isotopic signature of fatty acids, sterols, and alcohols in the scleractinian coral Turbinaria reniformis (2011, background): “Provision of essential nutrients through photosynthesis decreases, and the host has, therefore, either to rely on its reserves to sustain its metabolism ( Grottoli et al. 2004; Rodrigues and Grottoli 2007 )o r to acquire nutrients from heterotrophy.”
Metabolite profiling of symbiont and host during thermal stress and bleaching in the coral Acropora aspera (2017, background): “The beta-oxidation of lipid stores via the glyoxylate cycle is one such additional mechanism (Grottoli et al. 2004; DeSalvo et al. 2008; Imbs and Yakovleva 2012).”
Lipid class composition of bleached and recovering Porites compressa Dana, 1846 and Montipora capitata Dana, 1846 corals from Hawaii (2008, background): “…et al., 1993), zooxanthellae productivity (Patton et al., 1977; Stimson, 1987; Oku et al., 2003a), metabolic requirements (Crossland et al., 1980; Oku et al., 2002), food availability (Crossland et al., 1980), mucus production (Crossland et al., 1980) and bleaching status (Grottoli et al., 2004).”
Characterization of fatty acid composition in healthy and bleached corals from Okinawa, Japan (2006, background): “Bleached corals show decreased algal densities, chl a and host tissue biomass (Porter et al. 1989; Szmant and Gassman 1990; Fitt et al. 1993; Allison et al. 1996; Suzuki et al. 2000, 2003; Grottoli et al. 2004) impaired photosynthesis (Tchernov et al. 2004), a net decrease in photosynthesis (Warner ”
Energetics approach to predicting mortality risk from environmental stress: a case study of coral bleaching (2009, background): “Dynamics of lipid stores vs. coral energetics There is only limited experimental data available to test the relationship between changes in the coral energy budget and the size of colony lipid stores (Porter et al. 1989b; Grottoli et al. 2004; Anthony et al. 2007; Rodrigues & Grottoli 2007).”
Energy reserves and metabolism as indicators of coral recovery from bleaching (2007, methodology): “All measurements were made on whole coral samples (skeleton + animal tissue + zooxanthellae) ground with a mortar and pestle and normalized to total ash-free dry tissue biomass of the organic fraction (animal tissue + zooxanthellae) according to Grottoli et al. (2004).”
Enhanced energy status of corals on coastal, high-turbidity reefs (2006, background): “The role of temperature on energetics is complex, in that high temperature may promote anabolic processes (growth), but may also induce bleaching, which leads to reduced energy status (e.g. Grottoli et al. 2004).”
Major bleaching events can lead to increased thermal tolerance in corals (2008, background): “( Grottoli et al. 2004; Anthony et al. 2007), depending on the trophic plasticity of the coral species.”
Heterotrophic and autotrophic assimilation of fatty acids by two scleractinian corals, Montastraea faveolata and Porites astreoides (2011, background): “Corals require fatty acids to live and reproduce; fatty acids can function (1) as energy reserves (Grottoli et al. 2004), with saturated (SAFAs) and monounsaturated (MUFAs) fatty acids stored as triglycerides and wax esters (Oku et al.”
Influence of thermal history on the response of Montastraea annularis to short-term temperature exposure (2005, background): “Grottoli et al. (2004) suggested that differences in the P/R of Porites compressa and M. verrucosa may reflect how they deplete their energy reserves and may identify corals more likely to survive a bleaching event.”
Response of two species of Indo-Pacific corals, Porites cylindrica and Stylophora pistillata, to short-term thermal stress: The host does matter in determining the tolerance of corals to bleaching (2009, methodology): “…the upregulation of antioxidant enzymes (Lesser, 1996; Lesser and Farrell, 2004; Lesser, 2006), host energy reserve utilization (Porter et al.,1989; Grottoli et al., 2004, 2006), and heterotrophic plasticity (Grotolli et al., 2006)—all presumably have underlying influences on any response to…”
Epidemiology of skeletal eroding band on the Great Barrier Reef and the role of injury in the initiation of this widespread coral disease (2008, background): “For example, reduced energetic reserves in bleached or otherwise compromised corals (Grottoli et al. 2004) may limit investment in boundary maintenance or impair wound healing (Meesters and Bak 1993; Fine et al. 2002), increasing the susceptibility of coral hosts to ciliate infections.”