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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.1984.048.348.17</article-id>
<title-group>
<article-title>Secondary Ilvaite in a Dolerite Dyke from Rogaland, SW Norway</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Barton</surname>
<given-names>Michael</given-names>
</name></contrib>
<contrib contrib-type="author">
<name>
<surname>van Bergen</surname>
<given-names>Manfred J.</given-names>
</name></contrib>
<aff>Vening-Meinesz Laboratory, Department of Geochemistry, Institute for Earth Sciences, State University of Utrecht, Budapestlaan 4, 3584 CD Utrecht, The Netherlands</aff></contrib-group>
<pub-date pub-type="ppub">
<month>9</month>
<year>1984</year>
</pub-date>
<volume>48</volume>
<issue>348</issue>
<fpage>449</fpage>
<lpage>456</lpage>
<history>
<date date-type="received">
<day>15</day>
<month>8</month>
<year>1983</year>
</date>
<date date-type="rev-recd">
<day>20</day>
<month>12</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>Ilvaite is an alteration product of carbonate, which itself replaced clinopyroxene, in a Precambrian tholeiitic dyke. Additional secondary minerals are ferroactinolite, cummingtonite, chlorite, biotite, prehnite, and epidote. Microprobe analyses demonstrate that the ilvaite is close to the ideal end-member composition <inline-formula><mml:math>
<mml:mrow>
<mml:mo stretchy='false'>[</mml:mo><mml:msubsup>
<mml:mo>CaFe</mml:mo>
<mml:mn>2</mml:mn>
<mml:mrow>
<mml:mn>2</mml:mn><mml:mo>+</mml:mo>
</mml:mrow>
</mml:msubsup>
<mml:msup>
<mml:mo>Fe</mml:mo>
<mml:mrow>
<mml:mn>3</mml:mn><mml:mo>+</mml:mo>
</mml:mrow>
</mml:msup>
<mml:msub>
<mml:mo>Si</mml:mo>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:msub>
<mml:mo>O</mml:mo>
<mml:mn>8</mml:mn>
</mml:msub>
<mml:mo stretchy='false'>(</mml:mo><mml:mo>OH</mml:mo><mml:mo stretchy='false'>)</mml:mo><mml:mo stretchy='false'>]</mml:mo>
</mml:mrow>
</mml:math>
</inline-formula> and that only cummingtonites, Mg/(Mg+Fe<sup>2+</sup>) 0.77&#x2013;0.39, and carbonates (solid solutions between calcite and dolomite, dolomite and ankerite, magnesite and siderite) show significant compositional variations. It is estimated that ilvaite formed at temperatures &#x003C; 470 &#x00B0;C and at pressures &#x003C; 2 kbar, probably during a low-grade metamorphic event (or events) associated with the Caledonian orogeny. The fluids involved in the alteration process contained both CO<sub>2</sub> and H<sub>2</sub>O, initial fluids probably being richer in CO<sub>2</sub> than later ones. Ilvaite may be more common in hydrothermally altered igneous rocks than previously supposed.</p></abstract>
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