The use of proxy chemical records in Coral skeletons to ascertain past environmental conditions in Florida Bay

This paper will discuss the use of chemical proxies in coral skeletons to reconstruct the history of salinity (from the δ18O of the skeleton) and nutrients in the water (from the δ13C) in Florida Bay between 1824 and 1994. Monthly salinity and water temperature data collected since 1989 were used to establish a correlation between salinity, temperature, and the δ18O of the skeleton of the coralSolenastrea bournoni from Lignumvitae Basin in Florida Bay. This relationship explains over 50% of the variance in the δ18O of the skeleton. Assuming that interannual variations in the temperature of the water are small, we have applied this relationship to the δ18O measured in the coral skeleton collected from Lignumvitae Basin which has a record between 1824 and 1993. These data provide a revised estimate of salinity variation in Lignumvitae Basin for the period when historical records for salinity were not available, and show that the highest salinity events occurred in the past 30 yr. Using the relationships between the salinity in Lignumvitate Basin and other basins, obtained using a modern dataset, we are able to estimate ranges in salinity for other portions of Florida Bay. Skeletons of specimens of the coral speciesSiderastrea radians collected from other areas of Florida Bay show similar patterns in the δ18O over the past 10 yr, indicating that corals in most portions of Florida Bay are recording salinity variations in their skeletons and therefore support the idea that salinity variations in different portions of Florida Bay can be related. Fluorescence analysis of the coral from Lignumvitae Basin shows a large change in the magnitude of the 10-yr signal coincident with the construction of the railway, confirming that this event had a significant impact upon Florida Bay. The δ13C of the coral skeletons reveals a long-term history of the oxidation of organic material, fixation of carbon by photosynthesis (algal blooms), and the intrusion of marine water into the bay. Since the construction of the railway from Miami to Key West there has been a long-term decrease in the δ13C of the coral skeleton from Lignumvitae Basin, suggesting the increased oxidation of organic material in this area. This decrease in δ13C appears to have reached a minimum value around 1984 and has increased since this time in the western portions of Florida Bay. The increase may be related to the algal blooms prevalent in the area or alternatively could result from intrusion of more marine water. In the eastern areas, a small increase in the δ18C between 1984 and 1988 was followed by further decline suggesting more oxidation of organic material. We have also attempted to use the concentration of barium in the coral skeleton as a proxy indicator of the nutrient status in Florida Bay.

[1]  R. Halley,et al.  Reconstructing the History of eastern and Central Florida Bay using mollusk-shell isotope records , 1999 .

[2]  Ronald D. Jones,et al.  Seasonal and long-term trends in the water quality of Florida Bay (1989–1997) , 1999 .

[3]  G. Shimmield,et al.  Monsoon climate and Arabian Sea coastal upwelling recorded in massive corals from southern Oman , 1996 .

[4]  R. Dodge,et al.  The origin of variations in the isotopic record of scleractinian corals: II. Carbon , 1996 .

[5]  P. Kramer,et al.  The Stable Oxygen and Carbon Isotopic Record from a Coral Growing in Florida Bay: a 160 Year Record of Climatic and Anthropogenic Influence , 1996 .

[6]  P. Swart,et al.  Fiber-Optic-Based Sensing of Banded Luminescence in Corals , 1994 .

[7]  L. M. Walter,et al.  Depletion of 13C in seawater ΣC02 on modern carbonate platforms: Significance for the carbon isotopic record of carbonates , 1994 .

[8]  P. Swart,et al.  Geochemical evidence for groundwater behavior in an unconfined aquifer, south Florida , 1993 .

[9]  P. Swart,et al.  Fractionation of the stable isotopes of oxygen and carbon in carbon dioxide during the reaction of calcite with phosphoric acid as a function of temperature and technique , 1991 .

[10]  E. Boyle,et al.  Coralline barium records temporal variability in equatorial Pacific upwelling , 1989, Nature.

[11]  E. Boyle,et al.  Determination of lead, cadmium and other trace metals in annually-banded corals , 1988 .

[12]  A. Knap,et al.  Reef-building coral skeletons as chemical pollution (phosphorus) indicators , 1984 .

[13]  E. Boyle,et al.  On the Distribution of Copper, Nickel, and Cadmium in the Surface Waters of the North Atlantic , 1981 .

[14]  R. Dodge,et al.  Annual Periodicity of the 18O16O and 13C12C ratios in the coral Montastrea annularis , 1979 .

[15]  J. Edmond,et al.  Desorption of barium in the plume of the Zaire (Congo) river , 1978 .

[16]  J. Hanor,et al.  Non-conservative behavior of barium during mixing of Mississippi River and Gulf of Mexico waters , 1977 .

[17]  E. Boyle The marine geochemistry of trace metals , 1976 .

[18]  R. Dodge,et al.  Barium Chronologies from South Florida Reef Corals - Environmental Implications , 1997 .

[19]  G. T. Shen,et al.  Trace Element Indicators of Climate Variability in Reef-Building Corals , 1990 .

[20]  J. H. Hudson,et al.  A 107-year-old coral from Florida Bay: barometer of natural and man- induced catastrophes? , 1989 .

[21]  J. H. Hudson,et al.  Freshwater flow from the Everglades to Florida Bay: a historical reconstruction based on fluorescent banding in the coral Solenastrea bournoni , 1989 .

[22]  G. T. Shen Lead and cadmium geochemistry of corals : reconstruction of historic perturbations in the upper ocean , 1986 .

[23]  P. Isdale Fluorescent bands in massive corals record centuries of coastal rainfall , 1984, Nature.

[24]  P. Swart Carbon and oxygen isotope fractionation in scleractinian corals: a review , 1983 .