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Oxygen Isotope Measurements of Albite-Quartz-Zeolite Mineral Assemblages, Hokonui Hills, Southland, New Zealand

Published online by Cambridge University Press:  02 April 2024

Mary L. Stallard*
Affiliation:
Department of Geological Sciences, University of California, Santa Barbara, California 93106
J. R. Boles
Affiliation:
Department of Geological Sciences, University of California, Santa Barbara, California 93106
*
1Present address: Weiss Associates, 2938 McClure Avenue, Oakland, California 94609

Abstract

The oxygen isotopes of albite, quartz, and zeolites from the Hokonui Hills, New Zealand, constrain crystallization temperatures and the type of pore fluids present during diagenesis. A section of altered vitric tuffs in this region contains an extremely sharp reaction boundary between a heulandite-chlorite assemblage containing fresh detrital plagioclase and a laumontite-albite-quartz assemblage. A laumontite vein follows the local joint pattern and forms the reaction boundary, suggesting that laumontitization occurred as a result of fracturing and increased fluid flow during uplift. The albite (δ18O = +15.0)-quartz (δ18O = +19.9 to +20.5) geothermometer constrains the temperature of alteration between 145° and 170°C with a pore water δ18O of +1.8 to +3.5. The tuff was buried to an estimated maximum temperature of about 225°C, indicating that alteration occurred after maximum burial.

Framework oxygen was extracted from zeolites by reaction with ClF3 after the zeolites were thermally dehydrated in a vacuum. Laumontite was dehydrated at 300°C, and stilbite at 150°C. The precision of the method is typically about ±0.45‰. Fractionation curves for dehydrated zeolites are based on a general expression from the literature for feldspars, which depends only on the Si/Al ratio of the mineral. Measured δ18O values for laumontite in the groundmass of the altered tuff were +14.4‰. The laumontite-quartz pair constrains the temperature to between 139° and 162°C, in excellent agreement with the albite-quartz pair, and supporting the petrographic observation of co-crystallizing albite-laumontite.

Oxygen isotope values for fracture-filling laumontite in the vitric tuff, as well as those for groundmass and vein laumontite from other parts of the stratigraphic section, cluster around +14.5, suggesting that laumontite probably crystallized under similar conditions throughout much of the section. Oxygen isotope values for stilbite veins from various parts of the section indicate that this mineral crystallized at lower temperatures than the laumontite, for a given fluid isotopic composition, in agreement with the observed cross-cutting of laumontite by stilbite.

Type
Research Article
Copyright
Copyright © 1989, The Clay Minerals Society

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Footnotes

2

Presented at Symposium on the Geology, Genesis, Synthesis, and Use of Zeolites at 38th annual meeting of the Clay Minerals Society, Jackson, Mississippi, October 1986, convened by R. J. Donahoe. Manuscript reviewing and editing coordinated by R. J. Donahoe and R. A. Sheppard.

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