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<front>
<journal-meta>
<journal-id journal-id-type="archive">gsminmag</journal-id>
<journal-title>Mineralogical Magazine</journal-title>
<abbrev-journal-title abbrev-type="full">Mineralogical Magazine</abbrev-journal-title>
<issn pub-type="ppub">0026-461X</issn>
<publisher>
<publisher-name>Mineralogical Society</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.1180/minmag.1984.048.348.10</article-id>
<title-group>
<article-title>Mpororoite and Anthoinite from the Kara Mine, Tasmania</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Matsubara</surname>
<given-names>Satoshi</given-names>
</name></contrib>
<contrib contrib-type="author">
<name>
<surname>Kato</surname>
<given-names>Akira</given-names>
</name></contrib>
<aff>Department of Geology, National Science Museum, 3-23-1 Hyakunin-cho, Shinjuku, Tokyo 160, Japan</aff></contrib-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Nagashima</surname>
<given-names>Kozo</given-names>
</name>
<aff>Department of Chemistry, The University of Tsukuba, Sakura-mura, Ibaraki 305, Japan</aff></contrib></contrib-group>
<pub-date pub-type="ppub">
<month>9</month>
<year>1984</year>
</pub-date>
<volume>48</volume>
<issue>348</issue>
<fpage>397</fpage>
<lpage>400</lpage>
<history>
<date date-type="received">
<day>26</day>
<month>10</month>
<year>1983</year>
</date></history>
<copyright-statement>Copyright &#x00A9; 1984, The Mineralogical Society</copyright-statement>
<copyright-year>1984</copyright-year>
<abstract>
<title>Abstract</title>
<p>The first occurrence of mpororoite and anthoinite outside the African Continent has been found in an altered skarn from the Kara mine, Tasmania, forming a white powdery mixture of the two minerals pseudomorphing scheelite. The wet chemical analysis of the mixture shows WO<sub>3</sub>, Al<sub>2</sub>O<sub>3</sub>, and H<sub>2</sub>O to be the essential constituents, proving the non-essential nature of Fe<sub>2</sub>O<sub>3</sub> in mpororoite; the original mpororoite contained high Fe<sub>2</sub>O<sub>3</sub> substituting for Al<sub>2</sub>O<sub>3</sub>. The thermal treatment of the mixture at 100&#x00B0;C for 6 hours in air brings about the conversion of mpororoite into anthoinite, which re-hydrates into mpororoite, although the associated anthoinite does not. The source of Al is ascribed to the decomposition of aluminian andradite in the skarn.</p></abstract>
</article-meta>
</front>
</article>
