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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