The measurement of short-lived Ac to the open ocean would have to be included.Ac has so far been considered to behave similarly to Ra in the marine environment, with the exception of a strong Ac source in the deep-sea due to 231 Pa ex . Here, we present evidence of geochemical differences between Ac, which is retained in a warm vent system, and Ra, which is readily released (Moore et al., submitted). Another potential mechanism of producing deviations in 227 Ac/
228Ra and daughter isotope ratios from the expected production value of lithogenic material is observed at reducing environments, where enrichment in uranium may occur. The presented data here may serve as a reference for including 227 Ac in circulation models, and the overview provides values for some end-members that contribute to the global Ac distribution.
IntroductionActinium-227 is a naturally occurring radioisotope with a half-life of 21.77 years. It is generated by decay of protactinium-231, which is particularly abundant in deep-sea sediments. Actinium has a prominent source at the deep ocean floor, in conjunction with a half-life in the range of ocean mixing time scales, which makes it particularly useful as a tracer for deep mixing and upwelling studies (Geibert et al., 2002;Nozaki, 1984;Nozaki, 1993 So far, actinium has been mainly considered to behave in the ocean similarly to radium (Nozaki et al., 1990). Similar distribution coefficients of Ra and Ac in open ocean environments justify this assumption in many cases. However, actinium is expected to resemble the lanthanides in some aspects, like in its affinity for iron hydroxide, while radium is an alkaline earth metal that tends to be less particle reactive, but co-precipitates with
Material and Methods
Sampling and MeasurementOur data collection was produced with the radium delayed coincidence counting (RaDeCC) system (Moore and Arnold, 1996), which is routinely operated for the radiometrical determination of short-lived Ac data that was produced in different locations where short-lived Ra isotopes were measured (Figure 1).
Sampling locations
HawaiiTwo different types of samples were collected in the vicinity of Hawaii (Figure 4). A set of samples was taken in nearshore surface waters, at locations that are influenced by freshwater inputs to various degrees, as seen in the salinities of these samples. For a more detailed description of these sampling locations and the radium data, see (
Yucatan/ MexicoBrackish groundwater, lagoon water, and water from the shallow coastal ocean were
Puerto RicoOff the north eastern coast of Puerto Rico, a number of Ac data from deep waters near the sea floor along the slope of the island are presented (Figure 6). In contrast to most other sites shown here, these sample locations are not influenced by release from the continental shelf or freshwater/groundwater mixing effects, but they are representing open ocean values in the vicinity of slope sediments.
Israel, Gulf of AqabaSamples from the Israeli coast of the Red Sea near Elat ( Figur...