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Ewart, A. (1967) Pyroxene and magnetite phenocrysts from the Taupo quaternary rhyolitic pumice deposits, New Zealand. Mineralogical Magazine and Journal of the Mineralogical Society, 36 (278) 180-194 doi:10.1180/minmag.1967.036.278.02

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Reference TypeJournal (article/letter/editorial)
TitlePyroxene and magnetite phenocrysts from the Taupo quaternary rhyolitic pumice deposits, New Zealand
JournalMineralogical Magazine and Journal of the Mineralogical Society
AuthorsEwart, A.Author
Year1967 (June)Volume36
Issue278
PublisherMineralogical Society
Download URLhttps://rruff.info/doclib/MinMag/Volume_36/36-278-180.pdf+
DOIdoi:10.1180/minmag.1967.036.278.02Search in ResearchGate
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Mindat Ref. ID6061Long-form Identifiermindat:1:5:6061:9
GUID0
Full ReferenceEwart, A. (1967) Pyroxene and magnetite phenocrysts from the Taupo quaternary rhyolitic pumice deposits, New Zealand. Mineralogical Magazine and Journal of the Mineralogical Society, 36 (278) 180-194 doi:10.1180/minmag.1967.036.278.02
Plain TextEwart, A. (1967) Pyroxene and magnetite phenocrysts from the Taupo quaternary rhyolitic pumice deposits, New Zealand. Mineralogical Magazine and Journal of the Mineralogical Society, 36 (278) 180-194 doi:10.1180/minmag.1967.036.278.02
In(1966) Mineralogical Magazine Vol. 36 (278) Mineralogical Society
Abstract/NotesSummaryChemical data are presented for four hypersthenes and one coexisting hypersthene-augite pair, and chemical, X-ray, and thermomagnetic data presented for five titaniferous magnetites, all from various horizons of the Taupo pumice sequence. These phenocrysts are regarded as primary crystallization products, and not of xenocrystic origin. The hypersthenes range from Mg46·4Fe51·4Ca2·2 to Mg65·7Fe31·2Ca3·1; the augite composition is Mg48·5Fe12·3Ca39·2. The occurrence of such magnesian pyroxenes may be explained by the early separation of titaniferous magnetite, although it is also possible that the initial iron ratios of the liquids were already sufficiently low to precipitate these pyroxenes.The magnetites exhibit varying stages of oxidation. Data on the least oxidized specimens indicate they were initially magnetite-ulvöspinel solid solutions, with 40 to 50% (mol.) solid solution ulvöspinel. Subsequent oxidation has modified their compositions; there is some evidence that this could have occurred during normal weathering processes.


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