TRACE-ELEMENT PARTITIONING BETWEEN APATITE AND CARBONATITE MELT

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dc.contributor.author Klemme S.
dc.contributor.author Dalpé C.
dc.date.accessioned 2021-12-19T08:43:19Z
dc.date.available 2021-12-19T08:43:19Z
dc.date.issued 2003
dc.identifier https://www.elibrary.ru/item.asp?id=32174756
dc.identifier.citation American Mineralogist, 2003, 88, 4, 639-646
dc.identifier.issn 0003-004X
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/33627
dc.description.abstract To establish more fully a basis for quantifying the role of apatite in trace-element fractionation processes, hitherto unknown mineral/melt partition coefficients (Dapatite/melt) for a variety of trace elements (Li, Be, B, K, Cs, Rb, Ba, Th, U, Nb, Ta, La, Ce, Sr, Pr, Hf, Zr, Sm, Gd, Y, Lu, and Pb) have been measured between fluorapatite [Ca5(PO4)3F], chlorapatite [Ca5(PO4)3Cl], and hydroxylapatite [Ca5(PO4)3OH] and carbonatite melt. Apatites were equilibrated experimentally with carbonatite melts at 1 GPa and 1250 ∞C, and run products were analyzed for trace elements by secondary ion mass spectrometry (SIMS) and by laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS). Calculated partition coefficients indicate incompatibility of most analyzed elements. Rare-earth element (REE) partition coefficients show a convex-upward pattern, indicating that apatite prefers the middle (Sm, Gd) relative to the lighter (La, Ce, Pr) and heavier REE (Lu). Comparison of partition coefficients determined in this study with previous results in silicate systems reveals a strong influence of melt chemistry on partition coefficients, namely decreasing partition coefficients with decreasing silica-content, and increasing Ca and P in melts.
dc.title TRACE-ELEMENT PARTITIONING BETWEEN APATITE AND CARBONATITE MELT
dc.type Статья


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