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Halogen geochemistry of the Great Dyke, Zimbabwe

Publication ,  Journal Article
Boudreau, AE; Love, C; Prendergast, MD
Published in: Contributions to Mineralogy and Petrology
December 1, 1995

Apatite from the Great Dyke of Zimbabwe is relatively rich in the hydroxy-fluorapatite end-members. The mole fraction of fluorapatite increases from approximately 40% in cumulates of the Ultramafic Sequence to over 60% in a sample near the top of the exposed Mafic Sequence. The chlorapatite component decreases from a typical high of 10-20 mole% in the Ultramafic Sequence to about 1% in the uppermost part of the Mafic sequence. However, within-sample variation may be as great as the entire stratigraphic variation. Halogen contents of marginal samples generally are similar to axial samples, but tend not to have as high Cl concentration and tend to OH-enrichment. Biotite compositions approach hydroxyl end-member compositions, and apatite-biotite OH-F exchange geothermometers give an average closure temperature of 564°C. Apatite from the Umvimeela Dyke, an unlayered dike that parallels the Great Dyke over much of its length, contains less Cl than is seen in the Ultramafic Sequence cumulates of the Great Dyke. While the overall stratigraphic trend is characterized by a decrease in the Cl/F ratio with stratigraphic height, within the P1 unit at the top of the Ultramafic Sequence there is a positive correlation between Cl and other incompatible elements such as Na and Ce. The apparent contradiction between the general stratigraphie trend of decreasing Cl/F ratio with fractionation and the apparent increase in Cl and other incompatible elements seen in the P1 unit can be explained by assuming that the Great Dyke magma chamber was degassing near its top, where confining pressure was lowest and Cl was preferentially lost to a separating volatile- rich fluid. As cumulates formed on the floor, they entrapped liquid that was increasingly depleted in Cl at the higher stratigraphic levels. However, at any given stratigraphie interval, either local fluid enrichment or the eventual crystallization of halogen-bearing minerals that incorporate the smaller F ion in preference to the larger Cl ion led to a local increase in the Cl/F ratio.

Duke Scholars

Published In

Contributions to Mineralogy and Petrology

DOI

ISSN

0010-7999

Publication Date

December 1, 1995

Volume

122

Issue

3

Start / End Page

289 / 300

Related Subject Headings

  • Energy
  • 4019 Resources engineering and extractive metallurgy
  • 3705 Geology
  • 3703 Geochemistry
  • 0499 Other Earth Sciences
  • 0403 Geology
  • 0402 Geochemistry
 

Citation

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Boudreau, A. E., Love, C., & Prendergast, M. D. (1995). Halogen geochemistry of the Great Dyke, Zimbabwe. Contributions to Mineralogy and Petrology, 122(3), 289–300. https://doi.org/10.1007/s004100050128
Boudreau, A. E., C. Love, and M. D. Prendergast. “Halogen geochemistry of the Great Dyke, Zimbabwe.” Contributions to Mineralogy and Petrology 122, no. 3 (December 1, 1995): 289–300. https://doi.org/10.1007/s004100050128.
Boudreau AE, Love C, Prendergast MD. Halogen geochemistry of the Great Dyke, Zimbabwe. Contributions to Mineralogy and Petrology. 1995 Dec 1;122(3):289–300.
Boudreau, A. E., et al. “Halogen geochemistry of the Great Dyke, Zimbabwe.” Contributions to Mineralogy and Petrology, vol. 122, no. 3, Dec. 1995, pp. 289–300. Scopus, doi:10.1007/s004100050128.
Boudreau AE, Love C, Prendergast MD. Halogen geochemistry of the Great Dyke, Zimbabwe. Contributions to Mineralogy and Petrology. 1995 Dec 1;122(3):289–300.
Journal cover image

Published In

Contributions to Mineralogy and Petrology

DOI

ISSN

0010-7999

Publication Date

December 1, 1995

Volume

122

Issue

3

Start / End Page

289 / 300

Related Subject Headings

  • Energy
  • 4019 Resources engineering and extractive metallurgy
  • 3705 Geology
  • 3703 Geochemistry
  • 0499 Other Earth Sciences
  • 0403 Geology
  • 0402 Geochemistry