Expulsion of zooxanthellae by symbiotic cnidarians from the Red Sea
By O. Hoegh‐Guldberg, L. McCloskey, L. Muscatine. Coral reefs, 2004
105 citations recorded by the source corpus.
Subfields: Ecology, Oceanography
View Paper: https://www.semanticscholar.org/paper/08b55354043f9b119043abe888b6cbb998248cd6
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Citations in the corpus
- Cell Biology of Cnidarian-Dinoflagellate Symbiosis (2012, background): “This, together with the relative constancy of expulsion under steady environmental conditions (332) and the stimulation of expulsion only under conditions of stress (123, 159, 160, 332, 345), led Smith and Muscatine (332) to propose that expulsion is associated with host cell turnover, consistent wi”
- Reef sponges facilitate the transfer of coral-derived organic matter to their associated fauna via the sponge loop (2017, background): “%) of coral mucus dissolves in the water column (Wild et al. 2004), and coral loss of fixed carbon due to expulsion of Symbiodinium is typically negligible (0.01%; Hoegh-Guldberg et al. 1987) compared with mucus release (up to ~40%; Crossland et al. 1980, Tremblay et al. 2012).”
- Interspecific comparison of the symbiotic relationship in corals with high and low rates of bleaching-induced mortality (2002, background): “The density of zooxanthellae (number of cells per square centimeter of coral tissue), the dry weight of tissue per square centimeter, the size of zooxanthellae, and the rate of release of zooxanthellae ( Hoegh-Guldberg et al. 1987; Stimson and Kinzie 1991; Titlyanov et al. 1996) were measured on co”
- Organic matter release by dominant hermatypic corals of the Northern Red Sea (2010, background): “stantly release endosymbiotic zooxanthellae to the surrounding seawater (Hoegh-Guldberg et al. 1987; Stimson and Kinzie 1991), which consequently add to the measured POM release.”