(Table 3) Li concentrations and isotopic compositions in foraminiferal shells, carbonate sediments, and associated pore waters from ODP Sites 131-806 and 138-851

An improved procedure for lithium isotope analysis using Li3PO4 as the ion source has been investigated for application to geological samples. The 7Li/6Li ratio is measured using double rhenium filament thermal ionization mass spectrometry in which isotopic fractionation is minimized at high temperatures. The method produces a stable, high intensity Li+ ion beam that allows measurement of nanogram quantities of lithium. This results in a reduction in sample size of up to 1000 times relative to that required for the established Li2BO2+ method while maintaining a comparable precision of better than 1? (1 sigma). Replicate analyses of the NBS L-SVEC Li2CO3 standard yielded a mean value of 12.1047+/-0.0043 (n=21), which is close to the reported absolute value of 12.02+/-0.03. Intercalibration with a wide range of geological samples shows excellent agreement between the Li3PO4 and Li2BO2+ techniques. Replicate analyses of seawater and a fresh submarine basalt display high precision results that agree with previous measurements. Taking advantage of the high ionization efficiency of the phosphate ion source, we have made the first measurements of the lithium concentration (by isotope dilution) and isotopic composition of calcareous foraminiferal tests and other marine carbonates. Preliminary results indicate that substantial lithium exchange occurs between carbonate sediments and their interstitial waters. In addition, a possible link between lithium paleoceanography and paleoclimate during the last 1000 ky may be derived from planktonic foraminiferal tests. This highly sensitive technique can be applied in the examination of low lithium reservoirs and thereby provide insight into some fundamental aspects of lithium geochemistry.

Stable isotope analysis on sediment core RC11-86

Oxygen isotope measurements have been made in foraminifera from over 60 deep-sea sediment cores. Taken together with the oxygen isotope measurements published by Emiliani from Caribbean and Equatorial Atlantic cores, this comprises a unique body of stratigraphic data covering most of the important areas of calcareous sediment over the whole world ocean. The oxygen isotopic composition of foraminifera from cores of Late Pleistocene sediment varies in a similar manner in nearly all areas; the variations reflect changes in the oxygen isotopic composition of the ocean. The oceans are mixed in about 1 ka so that ocean isotopic changes, resulting from fluctuations in the quantity of ice stored on the continents, must have occurred almost synchronously in all regions. Thus the oxygen isotope record provides an excellent means of stratigraphic correlation. Cores accumulated at rates of over about 5 cm/ka provide records of oxygen isotopic composition change that are almost unaffected by post-depositional mixing of the sediment. Thus they preserve a detailed record of the advance and retreat of the ice masses in the northern hemisphere, and provide a unique source of information for the study of ice-sheet dynamics.