Radium and thorium isotopes in the surface waters of the East Pacific and coastal Southern California

A fiber extraction technique is used to concentrate Ra and Th isotopes from 1000 liters or more of seawater. Natural²²⁶Ra and²³⁴Th are used as yield tracers. In the equatorial Pacific the²²⁸Ra activity of surface water varies from 20 to 1 dpm/1000 kg and generally decreases away from continental shelf areas. Across the Peru Current System, this decrease is modeled as one-dimensional diffusion and indicates the possibility of two flow regimes with distinct characteristic mixing lengths and apparent eddy diffusivities of 10⁵ and 10⁷ cm²/s. The perturbing effects of advection and equatorial upwelling west of the Galapagos Islands are noted. Off the coast of Southern California a vertical²²⁸Ra distribution gives an apparent diffusivity of 1.6 cm²/s for the upper thermocline.²²⁶Ra concentrations near the coast appear to be higher than the open ocean values at comparable depths, which may reflect supply of this isotope from continental shelf sediments and/or upwelling. The insoluble daughter/soluble parent activity ratios²²⁸Th/²²⁸Ra and²³⁴Th/²³⁸U in the equatorial Pacific surface water display latitudinal trends which may be correlated with productivity variations. Near the coast of California these ratios reflect the differing oceanographic conditions north and south of Pt. Conception indicating a mean chemical removal time constant on the order of 4 months for Th and other highly reactive elements within the Southern California Bight. The²³²Th content of seawater sampled is less than 0.1 μg/1000 1; most of the published values for seawater²³²Th could well be too high. A comparison of the two methods of determining²²⁸Ra (via²²⁸Ac and via²²⁸Th) made on 64 seawater samples shows that the time delay required by the²²⁸Th method is more than compensated by its better analytical simplicity and precision.