<p> This is a study of the groundwaters and their associated rocks and minerals from the Lac du Bonnet batholith at the Underground Research Laboratory (URL), Pinawa, Manitoba, to assess the water-rock interaction in crystalline rocks by using Sr, O and U-series isotopes. Emphasis is also placed on the development of the analytical techniques.</p> <p> A high precision analytical technique of U-series isotopes has been developed in this study by using solid-source mass spectrometry. A precision of better than 1% (2σ) is achieved in determining the 234U/238U and 230Th/234U ratios using 10^-8 g of U and 10^-11 g of 230Th. The potential applications of this method is demonstrated by dating small speleothem samples and the results agree well with those of α-spectrometry. This method also applies well
to precise determination of the 234U/238U ratios in groundwaters and igneous rocks and minerals using small quantities of samples. However, precise measurements of 230Th in igneous rocks and minerals are limited by the large 232Th tail in the Th mass spectrum. Even better precision is achievable if pure Th spike is used.</p> <p> An ICP-MS isotope dilution method is also developed for fast and precise determination of Sr concentrations in groundwater samples. A precision of 1% is routinely achieved by taking into account the dead-time effect of the Channel Electron Multiplier (CEM) and the sample-to-spike ratios.</p> <p> The isotope results of both the groundwaters and the host rocks and minerals have revealed the processes of water-rock interaction and water mixing through the history of the batholith. Strontium isotope systematics of the rocks and their constituent minerals have shown that Sr loss occurred on whole-rock scale during both the high-temperature alteration (about 2300 Ma ago) and the low-temperature alteration which lasted at least 450 Ma. The Sr loss is most pronounced in plagioclase of altered samples. Uranium-series results indicate the disequilibrium of both whole-rock samples and minerals, and migration of U on whole-rock scale in, at least, the last million years.</p> <p> The Sr and O isotopic results have shown that the groundwaters from the three sub-horizontal, successively deeper fracture zones (FZ) have distinct isotopic signature: 87Sr/86Sr= 0.715 to 0.719 and 𝛿18O=-13o/oo for FZ-3; 87Sr/86Sr= 0.720 to 0.729 and 𝛿18O=-13 to -20o/oo for FZ-2; 87Sr/86Sr= 0.730 to 0.738 and 𝛿18O=-13 to -17o/oo for FZ-1. Uranium-series results show that all the groundwaters are highly enriched in 234U and the 234U/238U activity ratios range from 2.6 to 7.7. Mixing of three groundwaters is indicated by the Sr and O isotopes and the elemental chemistry. The three end-members are fresh surface water, the deep fresh (possibly glacial melt) groundwater and the deep saline groundwater.</p> <p> Comparison between the rocks and associated groundwaters shows that Sr isotopic equilibrium exists between plagioclase of altered samples and the groundwaters. This similarity indicates the vulnerable mineral phase control, such as plagioclase in this case, of the isotopic signatures, hence, chemistry of the groundwaters.</p> / Thesis / Master of Science (MSc)
Identifer | oai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/19320 |
Date | 05 1900 |
Creators | Li, Wangxing |
Contributors | McNutt, R. H., Schwarcz, H. P., Geology |
Source Sets | McMaster University |
Language | en_US |
Detected Language | English |
Type | Thesis |
Page generated in 0.002 seconds