Calcification rate and the stable carbon, oxygen, and nitrogen isotopes in the skeleton, host tissue, and zooxanthellae of bleached and recovering Hawaiian corals

LJ Rodrigues, AG Grottoli - Geochimica et Cosmochimica Acta, 2006 - Elsevier
Geochimica et Cosmochimica Acta, 2006Elsevier
We tested the effectiveness of stable isotopes as recorders of physiological changes that
occur during coral bleaching and recovery. Montipora capitata and Porites compressa
fragments were bleached in outdoor tanks with seawater temperature raised to 30° C
(treatment corals) for one month. Additional fragments were maintained at 27° C in separate
tanks (control corals). After one month,(0 months recovery), buoyant weight was measured
and a subset of fragments was frozen. Remaining fragments were returned to the reef for …
We tested the effectiveness of stable isotopes as recorders of physiological changes that occur during coral bleaching and recovery. Montipora capitata and Porites compressa fragments were bleached in outdoor tanks with seawater temperature raised to 30°C (treatment corals) for one month. Additional fragments were maintained at 27°C in separate tanks (control corals). After one month, (0 months recovery), buoyant weight was measured and a subset of fragments was frozen. Remaining fragments were returned to the reef for recovery. After 1.5, 4, and 8 months, fragments were collected, measured for buoyant weight, and frozen. Fragments were analyzed for stable carbon and oxygen isotopic compositions of the skeleton (δ13Cs; δ18Os) and nitrogen and carbon isotopic compositions of the host tissue (δ15Nh; δ13Ch) and zooxanthellae (δ15Nz; δ13Cz). δ13Cs decreased immediately after bleaching in M. capitata, but not in P. compressa. δ18Os of both species failed to record the warming event. During the remaining months of recovery, δ13Cs and δ18Os were more enriched in treatment than control corals due to decreases in calcification and metabolic fractionation during that time. Increased δ15Nh of treatment P. compressa may be due to expelled zooxanthellae during bleaching and recovery. Increased δ15Nz at 1.5 months in treatment fragments of both species reflects the increased incorporation of dissolved inorganic nitrogen to facilitate mitotic cell division and/or chl a/cell recovery. Changes in δ13Ch and δ13Cz at 1.5 months in treatment M. capitata indicated a large increase in heterotrophically acquired carbon relative to photosynthetically fixed carbon. We experimentally show that isotopes in coral skeleton, host tissue and zooxanthellae can be used to verify physiological changes during bleaching and recovery, but their use as a proxy for past bleaching events in the skeletal record is limited.
Elsevier
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