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dc.contributor.authorSong, G.
dc.contributor.authorQin, K.
dc.contributor.authorLi, G.
dc.contributor.authorEvans, Noreen
dc.contributor.authorChen, A.L.
dc.date.accessioned2017-01-30T12:58:35Z
dc.date.available2017-01-30T12:58:35Z
dc.date.created2015-02-01T20:00:58Z
dc.date.issued2014
dc.identifier.citationSong, G. and Qin, K. and Li, G. and Evans, N. and Chen, A.L. 2014. Scheelite elemental and isotopic signatures: Implications for the genesis of skarn-type W-Mo deposits in the Chizhou Area, Anhui Province, Eastern China. American Mineralogist. 99 (2-3): pp. 303-317.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/27362
dc.identifier.doi10.2138/am.2014.4431
dc.description.abstract

Scheelite is well developed in hydrothermal deposits, providing a window into genetic processes and facilitating comparative studies, however, few studies have focused on characterizing scheelite in skarn-type W-Mo deposits. The primary ore mineral in the Jitoushan and Baizhangyan skarn-type W-Mo deposits (Anhui Province, Eastern China), scheelite was analyzed for major, trace, and rare earth element (REE) abundance and for Sr-Nd isotopes. The analysis revealed two unique geochemical characteristics that distinguish the scheelite from skarn-type W-Mo deposits to that from vein-type Au-W and porphyry-type W-Mo deposits: higher Mo content with a negative correlation between MoO3 and WO3 and a strong HREE depletion. Skarn-type scheelite mainly inherited REE signatures from ore-forming fluids, and the early precipitation of skarn minerals (e.g., garnet, diopside, and amphibole) has most likely resulted in the observed strong HREE depletion in scheelite and the decoupling of LREEs and HREEs. Of the numerous substitution mechanisms suggested by previous workers, 3Ca2+ = 2REE3+ + □Ca (where □Ca is a Ca-site vacancy) is preferred for the substitution of REE3+ for Ca2+ and in this study, particularly given the low salinity of ore fluids.As the scheelite Eu anomalies were inherited from ore-forming fluids with variable redox conditions and pH, the complex dEu/Mo correlation indicates that Mo increasingly entered the scheelite under oxidizing conditions and reached a maxim at dEu values of 0.8 to 1. In contrast, under reducing conditions, Mo contents in scheelite decrease gradually and Mo is precipitated as molybdenite as a result of the change in dominant valence state. Unlike the Sr-Nd isotope compositions of scheelite from vein-type Au-(W) and W-(Sb-Au) deposits, the scheelite from skarn-type W-Mo deposits has low (143Nd/144Nd)(t) (most <0.5125) and intermediate (87Sr/86Sr)(t) values (most between 0.708 and 0.715). The eNd(t) values of the scheelite varied from –16 to –12.3 in the Baizhangyan deposit and from –9.5 to –9.1 in the Jitoushan deposit, indicating that the ore-forming materials in the two W-Mo deposits were mainly derived from crustal sources.

dc.publisherMineralogical Society of America
dc.subjectscheelite
dc.subjectChizhou
dc.subjectSr-Nd isotope
dc.subjectW-Mo deposits
dc.subjectsubstitution
dc.subjecttrace element
dc.subjectSkarn-type
dc.subjectEu anomaly
dc.subjectREE
dc.titleScheelite elemental and isotopic signatures: Implications for the genesis of skarn-type W-Mo deposits in the Chizhou Area, Anhui Province, Eastern China
dc.typeJournal Article
dcterms.source.volume99
dcterms.source.startPage303
dcterms.source.endPage317
dcterms.source.issn0003-004X
dcterms.source.titleAmerican Mineralogist
curtin.departmentJohn de Laeter CoE in Mass Spectrometry
curtin.accessStatusFulltext not available


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