U and Th concentrations and isotope ratios in modern carbonates and waters from the Bahamas
U and Th concentrations and isotope ratios in modern carbonates and waters from the Bahamas
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DOI:
10.1016/j.gca.2003.10.005
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发表时间:
2004-04
影响因子:
5
通讯作者:
L. Robinson;N. Belshaw;G. Henderson
中科院分区:
文献类型:
--
作者:
L. Robinson;N. Belshaw;G. Henderson
The short residence times of Th and Pa in seawater make them very responsive to changes in the ocean environment. We use a new multi-ion-counting technique to make Th and Pa isotope measurements in seawaters from a near-shore environment in which oceanic chemical tracers are not overwhelmed by terrestrial inputs (the Bahamas). An unusual feature of the Bahamas setting is the shallow depth of water residing on the bank tops. These waters have significantly lower232Th/230Th (∼10,000) than those immediately adjacent to the banks (24,000–31,000) and a (231Pa/230Th) near the production ratio (∼0.1). The change in232Th/230Th and (231Pa/230Th) on the bank tops is explained by almost quantitative removal of Th and Pa by scavenging, and their replacement with a mixture of230Th and231Pa alpha-recoiled from the underlying carbonates, together with Th from dust dissolution. Analysis of a water profile in the Tongue of the Ocean, which separates the Great and Little Bahama Banks, allows us to trace the movement of bank-top water to depth. A distinct minimum in both232Th/230Th (∼13,000) and (231Pa/230Th) (∼0.5) is observed at ∼430 m and is interpreted to reflect density cascading of bank-top water with entrained carbonate sediment. These results suggest that Th and Pa can be used as water-mass tracers in near-shore environments. Uranium concentration measurements on the same waters demonstrate that U is conservative across a range in salinity of 2 psu, with a concentration of 3.33 ppb (at a salinity of 35). The incorporation of U and Th isotopes into marine carbonates has also been assessed by analyzing carbonate samples from the same location as these Bahamas waters. Such incorporation is critical for U-Th geochronology. U isotope analyses demonstrate that seawater δ234U averages 146.6 and does not vary by more than 2.5%o, and that carbonates capture this value. Additional high precision measurements (≈±1%o) on modern carbonates confirm that all oceans have identical δ234U. Modern marine carbonates are shown to have232Th/230Th ratios that reflect the local seawater in which they formed.