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Clay Mineralogy, Oxygen Isotope Geochemistry, and Water/Rock Ratio Estimates, Te Mihi Area, Wairakei Geothermal Field, New Zealand
- Ryan B. Libbey, Fred J. Longstaffe, Roberta L. Flemming
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- Journal:
- Clays and Clay Minerals / Volume 61 / Issue 3 / June 2013
- Published online by Cambridge University Press:
- 01 January 2024, pp. 204-217
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Dioctahedral clays from an active continental geothermal system have been studied to assess their usefulness as proxies of paleo-hydrological and thermal conditions in the subsurface. Drill cuttings from Well WK244 in the Te Mihi area of the Wairakei Geothermal Field, New Zealand, were analyzed to determine the mineralogical, morphological, and isotopic characteristics of hydrothermal clays in these samples. Mixed-layer illite-dioctahedral smectite (I-S) and R0 chlorite-trioctahedral smectite are the main clay minerals, with I-S clays varying downward from R1 to R3 ordering and 50 to >90% illite over 160 m. The proportion of illite in I-S correlates positively with downhole temperature (r = 0.98) and I-S morphology changes from high aspect ratio ribbons, laths, and hairy fibers to pseudo-hexagonal plates with depth. Swelling clay percentages determined using the methylene blue method show a strong positive correlation with %S in I-S (r = 0.91), validating use of methylene blue as a rapid field tool for characterizing the smectite to illite transition in this active geothermal environment. The oxygen isotopic composition of I-S (dd18OI-S) decreases systematically with depth, and mostly reflects a progressive increase in subsurface temperature during clay formation. Estimates of water/rock ratios calculated using δ18OI-S values display stratigraphic variability that corresponds to variations in permeability. Oxygen isotopic measurements of I-S are a useful tool for understanding reservoir and permeability evolution in such geothermal systems and their related fossil analogs.
Oxygen, hydrogen, and strontium isotope constraints on the origin of granites
- Hugh P. Taylor, Jr.
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- Journal:
- Transactions of the Royal Society of Edinburgh: Earth Sciences / Volume 79 / Issue 2-3 / 1988
- Published online by Cambridge University Press:
- 03 November 2011, pp. 317-338
- Print publication:
- 1988
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Oxygen isotope data are very useful in determining the source rocks of granitic magmas, particularly when used in combination with Sr, Pb, and Nd isotope studies. For example, unusually high δ18O values in magmas (δ18O> +8) require the involvement of some precursor parent material that at some time in the past resided on or near the Earth's surface, either as sedimentary rocks or as weathered or hydrothermally altered rocks. The isotopic systematics which are preserved in the Mesozoic and Cenozoic batholiths of western North America can be explained by grand-scale mixing of three broadly defined end-members: (1) oceanic island-arc magmas derived from a “depleted” (MORB-type?) source in the upper mantle (δ18O c. +6 and 87Sr/86Sr c. 0·703); (2) a high-18O (c. +13 to +17) source with a very uniform 87Sr/86Sr (c. 0·708 to 0·712), derived mainly from eugeosynclinal volcanogenic sediments and (or) hydrothermally altered basalts; and (3) a much more heterogeneous source (87Sr/86Sr c. 0·706 to 0·750, or higher) with a high δ18O (c. +9 to +15) where derived from supracrustal metasedimentary rocks and a much lower δ18O (c. +7 to +9) where derived from the lower continental crust of the craton. These end-members were successively dominant from W to E, respectively, within three elongate N–S geographic zones that can be mapped from Mexico all the way N to Idaho.
18O/16O studies (together with D/H analyses) can, however, play a more important and certainly a unique role in determining the origins of the aqueous fluids involved in the formation of granitic and rhyolitic magmas. Fluid-rock interaction effects are most clear-cut when low-18O, low-D meteoric waters are involved in the isotopic exchange and melting processes, but the effects of other waters such as seawater (with a relatively high δD c. 0) can also be recognised. Because of these hydrothermal processes, rocks that ultimately undergo partial melting may exhibit isotopic signatures considerably different from those that they started with. We discuss three broad classes of potential source materials of such “hydrothermal-anatectic” granitic magmas, based mainly on water/rock (w/r), temperature (T), and the length of time (t) that fluid-rock interaction proceeds: (Type 1) epizonal systems with a wide variation in whole-rock δ18O and extreme 18O/16O disequilibrium among coexisting minerals (e.g. quartz and feldspar); (Type 2) deeper-seated and (or) longer-lived systems, also with a wide spectrum of whole-rock δ18O, but with equilibrated 18O/16O ratios among coexisting minerals; (Type 3) thoroughly homogenised and equilibrated systems with relatively uniform δ18O in all lithologies. Low-18O magmas formed by melting of rocks altered in a Type 2 or a Type 3 meteoric-hydrothermal system are the only kinds of “hydrothermal-anatectic” granitic magmas that are readily recognisable in the geological record. Analogous effects produced by other kinds of aqueous fluids may, however, be quite common, particularly in areas of extensional tectonics and large-scale rifting. The greatly enhanced permeabilities in such fractured terranes make possible the deep convective circulation of ground waters and sedimentary pore fluids. The nature and origin of low-18O magmas in the Yellowstone volcanic field and the Seychelles Islands are briefly reviewed in light of these concepts, as is the development of high-D, peraluminous magmas in the Hercynian of the Pyrenees.