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Quantification of total and particulate dimethylsulfoniopropionate (DMSP) in five Bermudian coral species across a depth gradient
Authors:D M Yost  R Jones  C L Rowe and Carys Louise Mitchelmore
Institution:(1) Chesapeake Biological Laboratory, University of Maryland Center for Environmental Science, 1, Williams Street, P.O. Box 38, Solomons, MD 20688, USA;(2) Present address: Hawaii Institute of Marine Biology, School of Ocean and Earth Science and Technology, University of Hawaii, 46-007 Lilipuna Road, Kaneohe, HI 96744, USA;(3) Bermuda Institute of Ocean Sciences (BIOS), 17 Biological Lane, St Georges, GE01, Bermuda;(4) Australian Institute of Marine Science, The UWA Oceans Institute, 35 Stirling Highway, Crawley, WA, 6009, Australia;
Abstract:The symbiotic dinoflagellate microalgae of corals (Symbiodinium spp.) contain high concentrations of dimethylsulfoniopropionate (DMSP), a multifunctional metabolite commonly found in many species of marine algae and dinoflagellates. A photoprotective antioxidant function for DMSP and its breakdown products has often been inferred in algae, but its role(s) in the coral–algal symbiosis remains elusive. To examine potential correlations between environmental and physiological parameters and DMSP, total DMSP (DMSPt, from the host coral and zooxanthellae), particulate DMSP (DMSPp, from the zooxanthellae only), coral surface area, and total protein, as well as zooxanthellae density, chlorophyll concentration, cell volume and genotype (i.e., clade) were measured in five coral species from the Diploria-Montastraea-Porites species complex in Bermuda along a depth gradient of 4, 12, 18, and 24 m. DMSPt concentrations were consistently greater than DMSPp concentrations in all species suggesting the possible translocation of DMSP from symbiont to host. D. labyrinthiformis was notably different from the other corals examined, showing DMSPp and DMSPt increases (per coral surface area or tissue biomass) with increasing water depth. However, overall, there were no consistent depth-related patterns in DMSPp and DMSPt concentrations. Further research, investigating dimethylsulfide (DMS), dimethylsulfoxide, and acrylate levels and DMSP-lyase activity in correlation with other biomarker endpoints that have been shown to be depth (i.e., temperature and light) responsive are needed to substantiate the significance of these findings.
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