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Keywords = halogen fugacity

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16 pages, 10276 KiB  
Article
Biotite Geochemistry and Its Implication for the Difference in Mineralization in the Xiongcun Porphyry Cu–Au Ore District, Tibet
by Pan Tang, Juxing Tang, Xinghai Lang, Bin Lin, Fuwei Xie, Miao Sun, Faqiao Li, Jing Qi, Hao Cui, Mengdie Wang, Yan Xiong and Gang Tao
Minerals 2023, 13(7), 876; https://doi.org/10.3390/min13070876 - 29 Jun 2023
Cited by 4 | Viewed by 2772
Abstract
The Xiongcun Cu–Au ore district is in the southern middle Gangdese Metallogenic Belt, Tibet, and formed during Neo-Tethyan oceanic subduction. The Xiongcun ore district mainly comprises two deposits, the No. I and No. II deposits, which were formed by two individual mineralization events [...] Read more.
The Xiongcun Cu–Au ore district is in the southern middle Gangdese Metallogenic Belt, Tibet, and formed during Neo-Tethyan oceanic subduction. The Xiongcun ore district mainly comprises two deposits, the No. I and No. II deposits, which were formed by two individual mineralization events according to deposit geology and Re–Os isotopic dating of molybdenite. The No. I deposit is similar to a reduced porphyry copper–gold deposit, given the widespread occurrence of primary and/or hydrothermal pyrrhotite and common CH4-rich and rare N2-rich fluid inclusions. The No. II deposit, similar to classic oxidized porphyry copper–gold deposits, contains highly oxidized minerals, including magnetite, anhydrite, and hematite. The halogen chemistry of the ore-forming fluid from the No. I and No. II deposits is still unclear. Biotite geochemistry with halogen contents was used to investigate the differences in ore-forming fluid between the No. I and No. II deposits. Hydrothermal biotite from the No. I deposit, usually intergrown with sphalerite, is Mg-rich and classified as phlogopite and Mg-biotite, and hydrothermal biotite from the No. II deposit is classified as Mg-biotite. Hydrothermal biotite from the No. I deposit has significantly higher SiO2, MnO, MgO, F, Li, Sc, Zn, Rb, Tl, and Pb contents and lower Al2O3, FeOtot, Cl, Ba, Cr, V, Co, Ni, Y, Sr, Zr, Th, and Cu contents than the biotite from the No. II deposit. Hydrothermal biotites from the No. I and No. II deposits yield temperatures ranging from 230 °C to 593 °C and 212 °C to 306 °C, respectively. The calculated oxygen fugacity and fugacity ratios indicate that the hydrothermal fluid of the No. I deposit has a higher F content, oxygen fugacity, and log(fHF/fHCl) value and a lower log(fH2O/fHF) value than the hydrothermal fluid from the No. II deposit. The biotite geochemistry shows that the No. I and No. II deposits formed from different hydrothermal fluids. The hydrothermal fluid of the No. I deposit was mixed with meteoric waters containing organic matter, resulting in a decrease in oxygen fugacity and more efficient precipitation of gold. The No. I and No. II deposits were formed by a Cl-rich hydrothermal system conducive to transporting Cu and Au. The decreasing Cl, oxygen fugacity, and temperature may be the key factors in Cu and Au precipitation. Biotite geochemistry allows a more detailed evaluation of the halogen chemistry of hydrothermal fluids and their evolution within porphyry Cu systems. Full article
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31 pages, 17635 KiB  
Article
Petrogenesis of the Eudialyte Complex of the Lovozero Alkaline Massif (Kola Peninsula, Russia)
by Julia A. Mikhailova, Gregory Yu. Ivanyuk, Andrey O. Kalashnikov, Yakov A. Pakhomovsky, Ayya V. Bazai and Victor N. Yakovenchuk
Minerals 2019, 9(10), 581; https://doi.org/10.3390/min9100581 - 25 Sep 2019
Cited by 22 | Viewed by 4639
Abstract
The Lovozero Alkaline Massif intruded through the Archaean granite-gneiss and Devonian volcaniclastic rocks about 360 million years ago, and formed a large (20 × 30 km) laccolith-type body, rhythmically layered in its lower part (the Layered Complex) and indistinctly layered and enriched in [...] Read more.
The Lovozero Alkaline Massif intruded through the Archaean granite-gneiss and Devonian volcaniclastic rocks about 360 million years ago, and formed a large (20 × 30 km) laccolith-type body, rhythmically layered in its lower part (the Layered Complex) and indistinctly layered and enriched in eudialyte-group minerals in its upper part (the Eudialyte Complex). The Eudialyte Complex is composed of two groups of rocks. Among the hypersolvus meso-melanocratic alkaline rocks (mainly malignite, as well as shonkinite, melteigite, and ijolite enriched with the eudialyte-group minerals, EGM), there are lenses of subsolvus leucocratic rocks (foyaite, fine-grained nepheline syenite, urtite with phosphorus mineralization, and primary lovozerite-group minerals). Leucocratic rocks were formed in the process of the fractional crystallization of melanocratic melt enriched in Fe, high field strength elements (HFSE), and halogens. The fractionation of the melanocratic melt proceeded in the direction of an enrichment in nepheline and a decrease in the aegirine content. A similar fractionation path occurs in the Na2O-Al2O3-Fe2O3-SiO2 system, where the melt of the “ijolite” type (approximately 50% of aegirine) evolves towards “phonolitic eutectic” (approximately 10% of aegirine). The temperature of the crystallization of subsolvus leucocratic rocks was about 550 °C. Hypersolvus meso-melanocratic rocks were formed at temperatures of 700–350 °C, with a gradual transition from an almost anhydrous HFSE-Fe-Cl/F-rich alkaline melt to a Na(Cl, F)-rich water solution. Devonian volcaniclastic rocks underwent metasomatic treatment of varying intensity and survived in the Eudialyte Complex, some remaining unchanged and some turning into nepheline syenites. In these rocks, there are signs of a gradual increase in the intensity of alkaline metasomatism, including a wide variety of zirconium phases. The relatively high fugacity of fluorine favored an early formation of zircon in apo-basalt metasomatites. The ensuing crystallization of aegirine in the metasomatites led to an increase in alkali content relative to silicon and parakeldyshite formation. After that, EGM was formed, under the influence of Ca-rich solutions produced by basalt fenitization. Full article
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35 pages, 37397 KiB  
Article
The Influence of Thermal Differences and Variation of Cl–F–OH Ratios on Cu-Ni-PGE Mineralization in the Contact Aureole of the South Kawishiwi Intrusion, Duluth Complex
by Zsolt Benkó, Aberra Mogessie, Ferenc Molnár, Steven A. Hauck, Mark J. Severson and Karl Ettinger
Geosciences 2018, 8(12), 474; https://doi.org/10.3390/geosciences8120474 - 12 Dec 2018
Cited by 4 | Viewed by 4313
Abstract
In the contact metamorphic aureole of the Duluth Complex, Cu-Ni-PGE mineralization occurs locally up to 100 m from the intrusion-footwall contact (Spruce Road area), whereas elsewhere (Dunka Pit deposit) the footwall granite and metapelite (Serpentine deposit) are barren. This study aimed to understand [...] Read more.
In the contact metamorphic aureole of the Duluth Complex, Cu-Ni-PGE mineralization occurs locally up to 100 m from the intrusion-footwall contact (Spruce Road area), whereas elsewhere (Dunka Pit deposit) the footwall granite and metapelite (Serpentine deposit) are barren. This study aimed to understand the effect of temperature and halogen fugacity variations on the presence or absence of mineralization in these footwall units. The mafic mineral assemblages, two-pyroxene, titanium-in-quartz, and biotite-apatite thermometers indicate that temperatures could be as high as 920 °C in the mineralized areas of the footwall, whereas the maximum temperature was lower by about 100 °C in the unmineralized part of the intrusion. Variation of the halogen concentrations and fugacities was monitored with the analysis of halogen concentrations in biotite and apatite. Fluorine and chlorine concentrations in biotite increase as a function of the distance from contact in the mineralized drill core and decrease in the unmineralized zones. Chlorine concentrations in apatite increase parallel with the distance from contact in the mineralized zones, whereas fluorine concentrations show only minor variation. Concentrations of these elements may have had subtle effect on the partial melting in the footwall units and indirectly facilitated the infiltration of the sulfide liquid into the footwall. Full article
(This article belongs to the Special Issue Magmatic-Hydrothermal Ore Deposits)
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