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Isotope ratios tracers

Calhoun, J.A. Bates, T.S. (1989) Sulfur isotope ratios. Tracers of nonsea-salt sulfur in the remote atmosphere. In Saltzman E.S. Cooper W.J. (Eds) Biogenic Sulphur in the Environment. Washington, DC American Chemical Society, pp. 369-379. [Pg.354]

Tracers have been used to label fluids in order to track fluid movement and monitor chemical changes of the injected fluid. Radioactive materials are one class of commonly used tracers. These tracers have several drawbacks. One drawback is that they require special handling because of the danger posed to personnel and the environment. Another drawback is the alteration by the radioactive materials of the natural isotope ratio indigenous to the reservoir— thereby interfering with scientific analysis of the reservoir fluid characteristics. In addition, the half life of radioactive tracers tends to be either too long or too short for practical use. [Pg.227]

For precise measurement of isotopic composition by mass spectrometry, it is also common to use either a natural, known isotopic ratio to correct for instrumental mass fractionation (e g., internal normalization) or to add a tracer for this purpose. For example for natural uranium samples, one can use the natural U/ U of 137.88 to correct for fractionation. Alternatively, one can use an added double spike of ratio -unity... [Pg.27]

Cochran JK, Masque P (2003) Short-lived U/Th-series radionuclides in the ocean tracers for scavenging rates, export fluxes and particle dynamics. Rev Mineral Geochem 52 461-492 Cohen AS, O Nions RK (1991) Precise determination of femtogram quantities of radium by thermal ionization mass spectrometry. Anal Chem 63 2705-2708 Cohen AS, Belshaw NS, O Nions RK (1992) High precision uranium, thorium, and radium isotope ratio measurements by high dynamic range thermal ionization mass spectrometry. Inti J Mass Spectrom Ion Processes 116 71-81... [Pg.56]

Durand S, Chabaux F, Rihs S, Duringer P, Elsass P (2005) U isotope ratios as tracers of groundwater inputs into surface waters example of the Upper Rhine hydrosystem. Chem Geol 220 1-19... [Pg.119]

In principle to all elements at low (ppb) concentrations. Valuable for first look analysis, at solid samples. Isotopic ratio measurements can distinguish between sources of elements in tracer studies and environmental samples. Use in geological dating based upon isotopic ratios. [Pg.305]

The mass spectrum of CTC, shown in Figure 14 (42), is characterized by a reasonably intense molecular ion at m/e 478 with the concomitant isotope peak at P+2 representing one chlorine atom in the ring system. Although it has been suggested that this chlorine atom be employed as a tracer via the isotope ratio for detection of species containing... [Pg.122]

Schwab AB, O Connell ME, Long SE (1995) The use of lifiiium concenh ation data and isotopic ratios as hydrologic tracers in a first-order catchment. Geol Soc Am Prog Abst 27 A97 Schou M (1988) Lithium h eahnent of manic-depressive illness—Past, present and perspectives. J Am Med Ass 259 1834-1836... [Pg.194]

The high precision with which Mg isotope ratios can be measured using MC-ICPMS opens up new opportunities for using Mg as a tracer in both terrestrial and extraterrestrial materials. A key advance is the ability to resolve kinetic from equilibrium mass-dependent fractionation processes. From these new data it appears that Mg in waters is related to mantle and crustal reservoirs of Mg by kinetic fractionation while Mg in carbonates is related in turn to the waters by equilibrium processes. Resolution of different fractionation laws is only possible for measurements of Mg in solution at present laser ablation combined with MC-ICPMS (LA-MC-ICPMS) is not yet sufficiently precise to measure different fractionation laws. [Pg.228]

Using the three measured ratios, Ca/ Ca, Ca/ " Ca and Ca/ " Ca, three unknowns can be solved for the tracer/sample ratio, the mass discrimination, and the sample Ca/ Ca ratio (see also Johnson and Beard 1999 Heuser et al. 2002). Solution of the equations is done iteratively. It is assumed that the isotopic composition of the Ca- Ca tracer is known perfectly, based on a separate measurement of the pure spike solution. Initially it is also assumed that the sample calcium has a normal Ca isotopic composition (equivalent to the isotope ratios listed in Table 1). The Ca/ Ca ratio of the tracer is determined based on the results of the mass spectrometry on the tracer-sample mixture, by calculating the effect of removing the sample Ca. This yields a Ca/ Ca ratio for the tracer, which is in general different from that previously determined for the tracer. This difference is attributed to mass discrimination in the spectrometer ion source and is used to calculate a first approximation to the parameter p which describes the instrumental mass discrimination (see below). The first-approximation p is used to correct the measured isotope ratios for mass discrimination, and then a first-approximation tracer/sample ratio and a first-approximation sample CeJ Ca... [Pg.259]

The tracer-subtraction procedure adds negligible uncertainty to the measured CaJ Ca ratios. However, it is in fact essentially impossible to entirely eliminate the effects of instrumental mass discrimination for the measurements of either the Ca- Ca mixed tracer or for the standard Ca isotope ratios. Hence, it is necessary to have a standard material with an agreed-upon value of 5 Ca. At the time of writing of this article there is no such standard. [Pg.260]

The lead isotope ratios indicate an upper cmstal source for the lead and are consistent with mineralization at 800 Ma. Tracer isotopes in carbonates and chalcocite concentrates indicate that an external fluid altered the dolomitic unit changing its isotopic composition as well as deposited copper mineralisation. [Pg.262]

T1 isotope ratios might be also used as a tracer in mantle geochemistry (Nielsen et al. 2006 2007). Since most geochemical reservoirs except Fe-Mn marine sediments and low temperature seawater altered basalts are more or less invariant in T1 isotope composition, admixing af small amounts of either of these two components into the mantle should induce small T1 isotope fractionations in mantle derived rocks. And indeed, evidence for the presence of Fe-Mn sediments in the mantle underneath Hawaii was presented by Nielsen et al. (2006). [Pg.92]

Since hthium and boron isotope fractionations mainly occur during low temperature processes, Li and B isotopes may provide a robust tracer of surface material that is recycled to the mantle (Elhott et al. 2004). Heterogeneous distribution of subducted oceanic and continental crust in the mantle will thus result in variations in Li and B isotope ratios. Furthermore, dehydration processes active in subducdon zones appear to be of crucial importance in the control of Li and B isotope composition of different parts of the mantle. For the upper mantle as a whole Jeffcoate et al. (2007) gave an estimated 8 Li-value of 3.5%o. [Pg.110]

Hesse R, Egeberg PK, Frape SK (2006) Chlorine stable isotope ratios as tracer for pore-water ad-vection rates in a submarine gas-hydrate field implication for hydrate concentration. Geofluids 6 1-7... [Pg.248]

If both chemical concentration gradients and isotopic ratio gradients are present (e.g., basaltic melt with Sr/ Sr ratio of 0.705 and andesitic melt with Sr/ Sr ratio of 0.720), the homogenization of isotopic ratio is referred to as isotopic diffusion (Lesher, 1990 Van Der Laan et al., 1994), although some prefer to call it isotopic homogenization. If there are concentration gradients in both major and trace elements, the diffusion of the trace elements is referred to as trace element diffusion (Baker, 1989). Isotopic diffusion and trace element diffusion are really part of multicomponent diffusion, which is complicated to handle. Isotopic diffusion should not be confused with self-diffusion, and trace element diffusion should not be confused with tracer diffusion. [Pg.185]

Isotope ratio measurements are performed whenever the exact ratio, or abundance, of two or more isotopes of an element must be known. For example, the isotopic ratios of lead are known to vary around the world, so it is possible to determine the source of lead in paint, bullets and petrol by knowing the isotopic abundances of the four lead isotopes 204, 206, 207, 208. Another example is the use of stable isotopes as metabolic tracers, where an animal is both fed and injected with an element having artificially enriched isotopes and the fractional absorption of the element can be accurately determined. [Pg.131]

A multiple ion collector device is required for the simultaneous determination of separated ion beams in precise and accurate isotope ratio measurements in order to study, for example, isotope fine variation in Nature or during tracer experiments using enriched stable isotope tracers. In thermal ionization mass spectrometers or in ICP-MS, mostly a system of several Faraday cups (up to 16) and/or ion counters (electron multipliers) is applied. In the photographs in Figures 4.7 and 4.8 examples of multiple ion collector systems are shown from the mass spectrometers MC-ICP-MS... [Pg.111]


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