Colonies of the Caribbean coral Montastraea cavernosa (Linnaeus) that harbor endosymbiotic cyanobacteria can fix nitrogen, whereas conspecifics without these symbionts cannot. The pattern of nitrogen fixation is diurnal and maximum rates occur in the early morning and evening. An analysis of δ 15 N stable isotope data showed that the zooxanthellae, but not the animal tissue, from colonies with cyanobacteria preferentially use the products derived from nitrogen fixation, and that these zooxanthellae also have a greater DNA content per cell, suggesting that these cells are in the DNA synthesis (S) and gap (G 2 ) + mitosis (M) phase of their cell cyle and are preparing to undergo cell division. Since nitrogen fixation did not occur during those times of the day when hyperoxia is known to occur, low oxygen concentrations might be required to support cyanobacterial respiration and provide the energy needed to fix nitrogen because the reaction centers of these cyanobacteria are uncoupled from light harvesting accessory pigments and the photosynthetic electron transport chain. Consistent with this were the depleted δ 13 C stable isotope signatures in all compartments of those corals with symbiotic cyanobacteria, which show an increase in heterotrophy compared with samples of M. cavernosa without cyanobacteria. Using modeled underwater light fields and measurements of photosynthesis, we show that the amount of time in which nitrogen fixation in these corals can take place increases with depth and that the distribution of corals with symbiotic cyanobacteria is positively correlated with increasing depth. The results presented here show that the zooxanthellae of M. cavernosa acquire nitrogen from cyanobacterial nitrogen fixation. Given that nitrogen limitation has long been proposed to contribute to the stability of these symbiotic associations, the mechanism by which zooxanthellae symbiosis in these corals is maintained remains an important question and the subject of future study.

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Coral bleaching-the loss of symbiotic dinoflagellates-is initiated when corals are exposed to sea surface temperatures above the regional summer average and has been responsible for massive coral mortality episodes. The ability of symbionts to recolonize the host after bleaching may be critical in determining if a colony will recover or experience mortality. Here, following the serendipitous bleaching of specimens of Montastraea faveolata of known photosynthetic, spectroscopic, and genetic characteristics, we describe changes in photosynthesis and light utilization during the recovery process. Fully recovered M. faveolata had minimum quantum requirements (1/W max ) that are very close to the theoretical minimum, indicating that symbiotic corals are not only one of the most efficient light collectors in nature, but also use this energy with maximum efficiency. Analyses of the photosynthetic responses of M. faveolata throughout the recovery process indicate that during the early stages, the symbiont population exhibited characteristics consistent with acclimation to higher irradiance relative to fully recovered corals. The absorption spectra of bleached samples showed contributions of chlorophyll b (Chl b) associated with a biomass increase of the endolithic algae. The propagation of endolithic algae after bleaching may provide partial protection to the surviving symbionts from excessive radiation by reducing the reflectivity of the skeleton. Changes in the relative abundances of different symbiotic algae between recovered and unbleached colonies did not result in significant variations in photosynthetic and light utilization characteristics.

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