The St. Marcel manganese deposit, Val d’Aosta, Italy, lies within the ophiolite sequence of the Zermatt-Saas unit of the Piemonte nappe, and formed as a hydrothermal sediment at an oceanic spreading center. Eoalpine metamorphism to eclogite facies was followed by retrogression to lawsonite–glaucophane facies and Lepontine greenschist facies assemblages. The Mn-rich rocks contain a wide variety of clinopyroxenes in the Di–Jd–Ac plane. Massive pyroxene-rich rocks (±albite ±quartz) contain aegirine-jadeite and impure jadeite, zoned via chloromelanite to omphacite. Violet pyroxenes (“violan”) in veins and in massive braunite ore are diopside, omphacite or chloromelanite. Di-Ac pyroxenes are breakdown products of omphacite/chloromelanite, or form late veins. Manganacmite substitution reaches 13% in some violans. X-ray data on 18 samples show that C2/c structures extend along the Di–Ac and Di–Jd joins to at least Ac60; omphacites and an intermediate chloromelanite are of P type. Textural relations suggest that the various pyroxene compositions within each sample formed sequentially (zoning and/or replacement) through local changes in bulk composition, and should not be used to define solvi. The spread of all data points for 25 samples is consistent with a solvus between Jd60 and Jd85 on the Di–Jd join, but this gap closes at Ac > 20%.

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First page of Crystal chemistry of clinopyroxenes from the St. Marcel manganese deposit, Val d’Aosta, Italy
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