Halogen geochemistry of the Great Dyke, Zimbabwe

被引:44
作者
Boudreau, AE
Love, C
Prendergast, MD
机构
[1] Department of Geology, Duke University, Box 902237, Durham
[2] Greendale, Harare
关键词
D O I
10.1007/s004100050128
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
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 degrees 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 stratigraphic 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 stratigraphic 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.
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页码:289 / 300
页数:12
相关论文
共 36 条
[1]  
ANDERSON AT, 1974, GEOL SOC AM BULL, V85, P1485, DOI 10.1130/0016-7606(1974)85<1485:CSAWIM>2.0.CO
[2]  
2
[3]  
[Anonymous], 1989, MAGMATIC SULPHIDES Z
[4]   VARIATION IN THE COMPOSITION OF APATITE THROUGH THE MERENSKY CYCLIC UNIT IN THE WESTERN BUSHVELD COMPLEX [J].
BOUDREAU, AE ;
KRUGER, FJ .
ECONOMIC GEOLOGY AND THE BULLETIN OF THE SOCIETY OF ECONOMIC GEOLOGISTS, 1990, 85 (04) :737-745
[5]   VARIATION IN THE COMPOSITION OF APATITE IN THE MUNNI MUNNI COMPLEX AND ASSOCIATED INTRUSIONS OF THE WEST PILBARA BLOCK, WESTERN-AUSTRALIA [J].
BOUDREAU, AE ;
LOVE, C ;
HOATSON, DM .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1993, 57 (18) :4467-4477
[6]   CHLORINE AS AN EXPLORATION GUIDE FOR THE PLATINUM-GROUP ELEMENTS IN LAYERED INTRUSIONS [J].
BOUDREAU, AE .
JOURNAL OF GEOCHEMICAL EXPLORATION, 1993, 48 (01) :21-37
[7]   INVESTIGATIONS OF THE STILLWATER COMPLEX .5. APATITES AS INDICATORS OF EVOLVING FLUID COMPOSITION [J].
BOUDREAU, AE ;
MCCALLUM, IS .
CONTRIBUTIONS TO MINERALOGY AND PETROLOGY, 1989, 102 (02) :138-153
[8]   HALOGEN GEOCHEMISTRY OF THE STILLWATER AND BUSHVELD COMPLEXES - EVIDENCE FOR TRANSPORT OF THE PLATINUM-GROUP ELEMENTS BY CL-RICH FLUIDS [J].
BOUDREAU, AE ;
MATHEZ, EA ;
MCCALLUM, IS .
JOURNAL OF PETROLOGY, 1986, 27 (04) :967-986
[9]  
BOUDREAU AE, 1995, MINERAL ASS CAN SHOR, V26, P25
[10]  
BOUDREAU AE, 1993, GEOL SOC AM ABSTR, V25, pA372