Microbialites and lipid biomarker from coral reefs off the volcanic islands Tahiti and Vanuatu and from the nonvolcanic sites Belize and the Maldives
Cobertura |
MEDIAN LATITUDE: 5.976643 * MEDIAN LONGITUDE: 157.193247 * SOUTH-BOUND LATITUDE: -20.000000 * WEST-BOUND LONGITUDE: 72.983300 * NORTH-BOUND LATITUDE: 18.000000 * EAST-BOUND LONGITUDE: -88.250000 * DATE/TIME START: 2005-10-29T01:38:00 * DATE/TIME END: 2005-11-13T03:45:00 |
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Data(s) |
25/04/2012
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Resumo |
The occurrence of microbialites in post-glacial coral reefs has been interpreted to reflect an ecosystem response to environmental change. The greater thickness of microbialites in reefs with a volcanic hinterland compared to thinner microbial crusts in reefs with a non-volcanic hinterland led to the suggestion that fertilization of the reefal environment by chemical weathering of volcanic rocks stimulated primary productivity and microbialite formation. Using a molecular and isotopic approach on reef-microbialites from Tahiti (Pacific Ocean), it was recently shown that sulfate-reducing bacteria favored the formation of microbial carbonates. To test if similar mechanisms induced microbialite formation in other reefs as well, the Tahitian microbialites are compared with similar microbialites from coral reefs off Vanuatu (Pacific Ocean), Belize (Caribbean Sea, Atlantic Ocean), and the Maldives (Indian Ocean) in this study. The selected study sites cover a wide range of geological settings, reflecting variable input and composition of detritus. The new lipid biomarker data and stable sulfur isotope results confirm that sulfate-reducing bacteria played an intrinsic role in the precipitation of microbial carbonate at all study sites, irrespective of the geological setting. Abundant biomarkers indicative of sulfate reducers include a variety of terminally-branched and mid chain-branched fatty acids as well as mono-O-alkyl glycerol ethers. Isotope evidence for bacterial sulfate reduction is represented by low d34S values of pyrite (-43 to -42 per mill) enclosed in the microbialites and, compared to seawater sulfate, slightly elevated d34S and d18O values of carbonate-associated sulfate (21.9 to 22.2 per mill and 11.3 to 12.4 per mill, respectively). Microbialite formation took place in anoxic micro-environments, which presumably developed through the fertilization of the reef environment and the resultant accumulation of organic matter including bacterial extracellular polymeric substances (EPS), coral mucus, and marine snow in cavities within the coral framework. ToF-SIMS analysis reveals that the dark layers of laminated microbialites are enriched in carbohydrates, which are common constituents of EPS and coral mucus. These results support the hypothesis that bacterial degradation of EPS and coral mucus within microbial mats favored carbonate precipitation. Because reefal microbialites formed by similar processes in very different geological settings, this comparative study suggests that a volcanic hinterland is not required for microbialite growth. Yet, detrital input derived from the weathering of volcanic rocks appears to be a natural fertilizer, being conductive for the growth of microbial mats, which fosters the development of particularly abundant and thick microbial crusts. |
Formato |
application/zip, 2 datasets |
Identificador |
https://doi.pangaea.de/10.1594/PANGAEA.810436 doi:10.1594/PANGAEA.810436 |
Idioma(s) |
en |
Publicador |
PANGAEA |
Relação |
Heindel, Katrin; Birgel, Daniel; Brunner, Benjamin; Thiel, Volker; Westphal, Hildegard; Gischler, Eberhard; Ziegenbalg, Simone B; Cabioch, Guy; Sjovall, Peter; Peckmann, Jörn Ludwig (2012): Post-glacial microbialite formation in coral reefs of te Pacific, Atlantic, and Indian Oceans. Chemical Geology, 304, 117-130, doi:10.1016/j.chemgeo.2012.02.009 |
Direitos |
CC-BY: Creative Commons Attribution 3.0 Unported Access constraints: unrestricted |
Palavras-Chave | #10Me-C16:0; 10-methyl-Hexadecanoic acid; 12-methyl-Tetradecanoic acid; 12-methyl-Tetradecanoic acid, d13C; 13-methyl-Tetradecanoic acid; 13-methyl-Tetradecanoic acid, d13C; 15-methyl-Hexadecanoic acid; ai-15:0; ai-15:0 d13C; ai-C17:0; ai-C17:0 d13C; anteiso-C17:0; anteiso-fatty acid C17:0; anteiso-fatty acid C17:0, d13C; Area; Area/locality; bulk non-carb.; C14:0; C15:0; C16:0; C16:0, d13C; C17:0; C18:0; C18:0, d13C; CaCO3; Calcium carbonate; Carbon, organic, total; CAS; Center for Marine Environmental Sciences; Chromium reducible sulfides; Comment; CRS; CRS non-carb.; d13C bound lipids; d13C Corg; d18O carb; d34S; delta 13C, bound lipids; delta 13C, organic carbon; delta 18O, carbonate; delta 34S; Depth; DEPTH, sediment/rock; Element analyser CS, LECO CS-200; Event; FA d13C; Fatty acids, d13C; Gasbench II (Thermo) coupled to a DELTA V plus IRMS; Gas chromatography - Mass spectrometry (GC-MS); i-15:0; i-15:0 d13; i-17:0; Integrated Ocean Drilling Program / International Ocean Discovery Program; IODP; iso-C15:0; iso-C16:0; iso-C17:0; Label; MAGE; MARUM; Mass spectrometer Finnigan Delta-E; non-carb.; Non-isoprenoidal sn-1-mono-O-alkyl glycerol ethers; S; Sample code/label; SRB lipids, Tahiti data from Heindel et al. (2010); Sulfur, total; Tahiti data from Heindel et al. (2010); TOC; TOC, Tahiti data from Heindel et al. (2010) |
Tipo |
Dataset |