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12<br />

Geochemisches Zentrallabor, Universität Tübingen, Germany. Sr was loaded with a Ta-<br />

HF activator on pre-conditioned W filaments and measured in single-filament mode. Nd<br />

was loaded as phosphate on pre-conditioned Re filaments and measurements were<br />

performed in a Re double filament configuration. The 87 Sr/ 86 Sr isotope ratios were<br />

normalised to 86 Sr/ 88 Sr = 0.1194 and the 143 Nd/ 144 Nd isotope ratios to 146 Nd/ 144 Nd =<br />

0.7219. Analyses of 24 separate loads of Ames metal (Geological Survey of Canada,<br />

Roddick et al. 1992) gave a 143 Nd/ 144 Nd of 0.512125 ± 0.000010 (errors are 2� of the<br />

mean) and within the same period the NBS 987 Sr standard yielded a 87 Sr/ 86 Sr of<br />

0.710259 ± 0.000012 (n = 28). Total procedural blanks (chemistry and loading) were <<br />

200 pg for Sr and < 50 pg for Nd. Sm and Nd isotopic ratios of 17 samples are given in<br />

Appendix A, Tab. A6.<br />

2.5 U/Pb isotope dilution and Pb/Pb evaporation age determination methods on<br />

zircons<br />

For conventional U/Pb analyses zircon populations consisting of a few<br />

morphologically identical grains were washed in hot 6 N HCl and hot 7 N HNO3 prior to<br />

dissolution to remove surface contamination. A mixed 205 Pb/ 235 U tracer solution was<br />

added to the grains. Dissolution was performed in PTFE vessels in a 1900 psig (130<br />

bar) PARR acid digestion bomb (Parrish 1987) according to the vapour digestion<br />

method (Wendt & Todt 1991). The bomb was placed in a temperature-controlled oven<br />

at 200°C for one week in 22N HF and for one day in 6N HCl to assure re-dissolution of<br />

the fluorides into chloride salts and avoid U/Pb fractionation (Mattinson 1994).<br />

Separation and purification of U and Pb were carried out on Teflon columns with a 40 �l<br />

bed of AG1-X8 (100-200 mesh) anion exchange resin following the procedure described<br />

in Poller et al. (1997). Further details on U/Pb analytical techniques are given in Chen et<br />

al. (2000).<br />

Thermal Ionization Mass Spectrometry was applied for isotopic measurements of 11<br />

samples on a Finnigan MAT 262 mass spectrometer at the Geochemisches Zentrallabor,<br />

Universität Tübingen, Germany. The measurements were performed by Fukun<br />

Chen, Wolfgang Siebel, and myself. Four samples were measured at the Isotope<br />

Geochemistry Lab of the University of Washington, USA, by Bruce K. Nelson. Pb was<br />

loaded onto a pre-conditioned Re filament according to the Si-gel method (Cameron et<br />

al. 1969) and measured at ~1300°C in single-filament mode. U was loaded with 1N<br />

HNO3 onto a pre-conditioned Re filament and was measured in double-filament<br />

configuration. Total procedural blanks were < 10 pg for Pb and < 2 pg for U. A factor of<br />

1‰ per mass unit for instrumental mass fractionation was applied to all Pb analyses,<br />

using NBS SRM 981 as reference material. Initial common Pb remaining after correction<br />

for tracer and blank was corrected using values from the Stacey & Kramers (1975)<br />

model. The decay constants for U are those given in Jaffey et al. (1971). U/Pb discordia<br />

intercepts were calculated using regression treatment (Wendt 1986).<br />

The single zircon Pb-evaporation analyses were made by Fukun Chen following the<br />

procedures of Kober (1986, 1987), Körner & Todt (1988), Cocherie et al. (1992), Klötzli<br />

(1997) and Kröner & Hegner (1998). Untreated whole zircon grains or fragments were<br />

analysed using a double Re filament configuration. The motif behind this method is the<br />

assumption that the Pb with the highest activation energy, i.e. the highest evaporation

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