(Table 2) Delta 14C record of sediment core Pulse-32_SMB

The D14C of surface water dissolved inorganic carbon (DIC) in the Southern California Bight was compared to D14C as recorded by the sterols in Santa Monica and Santa Barbara Basin sediments. All of the C26, C27, C28, and C29 sterols as well as dinosterol had 14C concentrations equal to surface water DIC, indicating that all of the major sterols were derived from phytoplanktonic production. There is no detectable terrestrial component. Their tracer capability was confirmed by comparing the "bomb 14C"-derived change in surface water D14CDIC with the change in D14Csterol. The "prebomb" D14CDIC was -82 per mil, and prebomb sterols averaged -75±19 per mil. The D14C value in 1996 was +71 per mil. Eighteen measurements representing eight different sterols from the sediment-water interface of both Santa Monica and Santa Barbara Basins averaged +62±23 per mil. When three of these values were eliminated because of suspected contamination, the remaining data averaged +71 ±12 per mil. The entire compound class could serve as an excellent proxy for the 14C concentration of ocean surface waters.

(Table 1, page 1376) Chemical analyses of manganese nodules and crusts from the Pacific Ocean

A compilation of chemical analyses of Pacific Ocean nodules using an x-ray fluorescence technique. The equipment used was a General Electric XRD-5 with a tungsten tube. Lithium fluoride was used as the diffraction element in assaying for all elements above calcium in the atomic table and EDDT was used in conjunction with a helium path for all elements with an atomic number less than calcium. Flow counters were used in conjunction with a pulse height analyzer to eliminate x-ray lines of different but integral orders in gathering count data. The stability of the equipment was found to be excellent by the author. The equipment was calibrated by the use of standard ores made from pure oxide forms of the elements in the nodules and carefully mixed in proportion to the amounts of these elements generally found in the manganese nodules. Chemically analyzed standards of the nodules themselves were also used. As a final check, a known amount of the element in question was added to selected samples of the nodules and careful counts were taken on these samples before and after the addition of the extra amount of the element. The method involved the determination and subsequent use of absorption and activation factors for the lines of the various elements. All the absorption and activation factors were carefully determined using the standard ores. The chemically analyzed samples of the nodules by these methods yielded an accuracy to at least three significant figures.