scholarly journals Rutile and Chlorite Geochemistry Constraints on the Formation of the Tuwu Porphyry Cu Deposit, Eastern Tianshan and Its Exploration Significance

Minerals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 968
Author(s):  
Xingying Wen ◽  
Fangfang Zhang ◽  
Yinhong Wang ◽  
Min Sun ◽  
Wei Zhang ◽  
...  

The chemical composition of rutile has been used as an indicator in magmatic and metamorphic-related diagenetic systems, but rarely in porphyry-style ore systems. The Tuwu deposit (557 Mt at 0.58% Cu) is a large porphyry-style Cu mineralization in Eastern Tianshan, Xinjiang, with typical disseminated, stockwork mineralized veins hosted in tonalite and diorite porphyry, and to a lesser extent in volcanic rocks of the Qi’eshan Group. We first present determination of rutile minerals coupled with chlorite identified in mineralized porphyries from Tuwu to reveal their geochemical features, thus providing new insights into the ore-forming processes and metal exploration. Petrographic and BSE observations show that the rutile generally occurs as large crystals (30 to 80 µm), in association with hydrothermal quartz, chlorite, pyrite, and chalcopyrite. The rutile grains display V, Fe, and Sn enrichment and flat LREE-MREE patterns, indicating a hydrothermal origin. Titanium in rutile (TiO2) is suggested to be sourced from the breakdown and re-equilibration of primary magmatic biotite and Ti-magnetite, and substituted by Sn4+, high field strength elements (HFSE; e.g., Zr4+ and Hf4+), and minor Mo4+ under hydrothermal conditions. The extremely low Mo values (average 30 ppm) in rutile may be due to rutile formation postdating that of Mo sulfides (MoS2) formation in hydrothermal fluids. Chlorite analyses imply that the ore-forming fluids of the main stage were weakly oxidized (logfO2 = −28.5 to −22.1) and of intermediate temperatures (308 to 372 °C), consistent with previous fluid inclusion studies. In addition, Zr-in-rutile geothermometer yields overestimated temperatures (>430 °C) as excess Zr is incorporated into rutile, which is likely caused by fast crystal growth or post crystallization modification by F-Cl-bearing fluid. Thus, application of this geothermometer to magmatic-hydrothermal ore systems is questionable. Based on the comparison of rutile characteristics of porphyry Cu with other types of ore deposits and barren rocks, we suggest that porphyry Cu-related rutile typically has larger grain size, is enriched in V (average 3408 ppm, compared to <1500 ppm of barren rocks) and to a lesser extent in W and Sn (average 121 and 196 ppm, respectively), and has elevated Cr + V/Nb + Ta ratios. These distinctive signatures can be used as critical indicators of porphyry-style Cu mineralization and may serve as a valuable tool in mineral exploration.

Author(s):  
Henrik Stendal ◽  
Wulf Mueller ◽  
Nicolai Birkedal ◽  
Esben I. Hansen ◽  
Claus Østergaard

NOTE: This article was published in a former series of GEUS Bulletin. Please use the original series name when citing this article, for example: Stendal, H., Mueller, W., Birkedal, N., Hansen, E. I., & Østergaard, C. (1997). Mafic igneous rocks and mineralisation in the Palaeoproterozoic Ketilidian orogen, South-East Greenland: project SUPRASYD 1996. Geology of Greenland Survey Bulletin, 176, 66-74. https://doi.org/10.34194/ggub.v176.5064 _______________ The multidisciplinary SUPRASYD project (1992–96) focused on a regional investigation of the Palaeoproterozoic Ketilidian orogenic belt which crosses the southern tip of Greenland. Apart from a broad range of geological and structural studies (Nielsen et al., 1993; Garde & Schønwandt, 1994, 1995; Garde et al., 1997), the project included a mineral resource evaluation of the supracrustal sequences associated with the Ketilidian orogen (e.g. Mosher, 1995). The Ketilidian orogen of southern Greenland can be divided from north-west to south-east into: (1) a border zone in which the crystalline rocks of the Archaean craton are unconformably overlain by Ketilidian supracrustal rocks; (2) a major polyphase pluton, referred to as the Julianehåb batholith; and (3) extensive areas of Ketilidian supracrustal rocks, divided into psammitic and pelitic rocks with subordinate interstratified mafic volcanic rocks (Fig. 1). The Julianehåb batholith is viewed as emplaced in a magmatic arc setting; the supracrustal sequences south of the batholith have been interpreted as either (1) deposited in an intra-arc and fore-arc basin (Chadwick & Garde, 1996), or (2) deposited in a back-arc or intra-arc setting (Stendal & Swager, 1995; Swager, 1995). Both possibilities are plausible and infer subduction-related processes. Regional compilations of geological, geochemical and geophysical data for southern Greenland have been presented by Thorning et al. (1994). Mosher (1995) has recently reviewed the mineral exploration potential of the region. The commercial company Nunaoil A/S has been engaged in gold prospecting in South Greenland since 1990 (e.g. Gowen et al., 1993). A principal goal of the SUPRASYD project was to test the mineral potential of the Ketilidian supracrustal sequences and define the gold potential in the shear zones in the Julianehåb batholith. Previous work has substantiated a gold potential in amphibolitic rocks in the south-west coastal areas (Gowen et al., 1993.), and in the amphibolitic rocks of the Kutseq area (Swager et al., 1995). Field work in 1996 was focused on prospective gold-bearing sites in mafic rocks in South-East Greenland. Three M.Sc. students mapped showings under the supervision of the H. S., while an area on the south side of Kangerluluk fjord was mapped by H. S. and W. M. (Fig. 4).


Minerals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 347
Author(s):  
Carsten Laukamp ◽  
Andrew Rodger ◽  
Monica LeGras ◽  
Heta Lampinen ◽  
Ian C. Lau ◽  
...  

Reflectance spectroscopy allows cost-effective and rapid mineral characterisation, addressing mineral exploration and mining challenges. Shortwave (SWIR), mid (MIR) and thermal (TIR) infrared reflectance spectra are collected in a wide range of environments and scales, with instrumentation ranging from spaceborne, airborne, field and drill core sensors to IR microscopy. However, interpretation of reflectance spectra is, due to the abundance of potential vibrational modes in mineral assemblages, non-trivial and requires a thorough understanding of the potential factors contributing to the reflectance spectra. In order to close the gap between understanding mineral-diagnostic absorption features and efficient interpretation of reflectance spectra, an up-to-date overview of major vibrational modes of rock-forming minerals in the SWIR, MIR and TIR is provided. A series of scripts are proposed that allow the extraction of the relative intensity or wavelength position of single absorption and other mineral-diagnostic features. Binary discrimination diagrams can assist in rapidly evaluating mineral assemblages, and relative abundance and chemical composition of key vector minerals, in hydrothermal ore deposits. The aim of this contribution is to make geologically relevant information more easily extractable from reflectance spectra, enabling the mineral resources and geoscience communities to realise the full potential of hyperspectral sensing technologies.


1972 ◽  
Vol 9 (1) ◽  
pp. 36-42 ◽  
Author(s):  
Calvert C. Bristol

X-ray powder diffraction methods, successful in quantitative determination of silicate minerals in fine-grained rocks, have been applied to the determination of calcite, dolomite, and magnesite in greenschist facies meta-volcanic rocks. Internal standard graphs employing two standards (NaCl and Mo) have been determined.Carbonate mineral modes (calcite and dolomite) for 6 greenschist facies meta-volcanic rocks obtained by the X-ray powder method have been compared to normative carbonate mineral contents calculated for the same rocks. This comparison showed a maximum variation of 7.7 wt.% between the X-ray modes and the normative carbonate mineral contents of the rocks. Maximum standard deviation for the X-ray modes of these rocks was equivalent to 4.4 wt.%.


2008 ◽  
Vol 37 (2) ◽  
pp. 146-150 ◽  
Author(s):  
Gloria Vaggelli ◽  
Alessandro Borghi ◽  
Silvia Calusi ◽  
Roberto Cossio ◽  
Lorenzo Giuntini ◽  
...  
Keyword(s):  

Author(s):  
Xuyang Meng ◽  
Jeremy P Richards ◽  
Daniel J Kontak ◽  
Adam C Simon ◽  
Jackie M Kleinsasser ◽  
...  

Abstract Most known porphyry Cu ± Au deposits are associated with moderately oxidized and sulfur-rich, calc-alkaline to mildly alkalic arc-related magmas in the Phanerozoic. In contrast, sodium-enriched tonalite-trondhjemite-granodiorite-diorite (TTG) magmas predominant in the Archean are hypothesized to be unoxidized and sulfur-poor, which together preclude porphyry Cu deposit formation. Here, we test this hypothesis by interrogating the causative magmas for the ~2.7 Ga TTG-related Côté Gold, St-Jude, and Clifford porphyry-type Cu ± Au deposit settings in the Neoarchean southern Abitibi subprovince. New and previously published geochronological results constrain the age of emplacement of the causative magmas at ~2.74 Ga, ~2.70 Ga, and ~2.69 Ga, respectively. The dioritic and trondhjemitic magmas associated with Côté Gold and St-Jude evolved along a plagioclase-dominated fractionation trend, in contrast to amphibole-dominated fractionation for tonalitic magma at Clifford. Analyses of zircon grains from the Côté Gold, St-Jude, and Clifford igneous rocks yielded εHf(t) ± SD values of 4.5 ± 0.3, 4.2 ± 0.6, and 4.3 ± 0.4, and δ18O ± SD values of 5.40 ± 0.11 ‰, 3.91 ± 0.13 ‰, and 4.83 ± 0.12 ‰, respectively. These isotopic signatures indicate that although these magmas are mantle-sourced with minimal crustal contamination, for the St-Jude and Clifford settings the magmas or their sources may have undergone variable alteration by heated seawater or meteoric fluids. Primary barometric minerals (i.e., zircon, amphibole, apatite, and magnetite-ilmenite) that survived variable alteration and metamorphism (up to greenschist facies) were used for estimating fO2 of the causative magmas. Estimation of magmatic fO2 values, reported relative to the fayalite-magnetite-quartz buffer as ΔFMQ, using zircon geochemistry indicate that the fO2 values of the St-Jude, Côté Gold, and Clifford magmas increase from ΔFMQ -0.3 ± 0.6, ΔFMQ +0.8 ± 0.4, to ΔFMQ +1.2 ± 0.4, respectively. In contrast, amphibole chemistry yielded systematically higher fO2 values of ΔFMQ +1.6 ± 0.3 and ΔFMQ +2.6 ± 0.1 for Côté Gold and Clifford, respectively, which are consistent with previous studies that indicate amphibole may overestimate the fO2 of intrusive rocks by up to one log unit. Micro X-ray absorption near edge structure (μ-XANES) spectrometric determination of sulfur (i.e., S6+/ΣS) in primary apatite yielded ≥ΔFMQ -0.3 and ΔFMQ +1.4–1.8 for the St-Jude and Clifford, respectively. The magnetite-ilmenite mineral pairs from the Clifford tonalite yielded ΔFMQ +3.3 ± 1.3 at equilibrium temperatures of 634 ± 21 °C, recording the redox state of the late stage of magma crystallization. Electron probe microanalyses revealed that apatite grains from Clifford are enriched in S (up to 0.1 wt. %) relative to those of Côté Gold and St-Jude (below the detection limit), which is attributed to either relatively oxidized or sulfur-rich features of the Clifford tonalite. We interpret these results to indicate the deposits at Côté Gold and Clifford formed from mildly (~ΔFMQ +0.8 ± 0.4) to moderately (~ΔFMQ +1.5) oxidized magmas where voluminous early sulfide saturation was probably limited, whereas the St-Jude deposit represents a rare case whereby the ingress of externally derived hydrothermal fluids facilitated metal fertility in a relatively reduced magma chamber (~ΔFMQ +0). Furthermore, we conclude that variable modes of formation for these deposits and, in addition, the apparent rarity of porphyry-type Cu-Au deposits in the Archean may be attributed to either local restriction of favorable metallogenic conditions, and/or preservation, or an exploration bias.


2019 ◽  
Vol 61 (1) ◽  
pp. 18-38
Author(s):  
L. B. Damdinova ◽  
B. B. Damdinov ◽  
M. O. Rampilov ◽  
S. V. Kanakin

This study examines the compositions of the ore and the ore formation solutions, conditions of formation, and sources of Be mineralization using the Aunikskoye F-Be deposit, which is an integral part of the Western Transbaikal beryllium-bearing provinces, as a representative example. Further, the main factors responsible for the formation of beryllium mineralization were evaluated. The ore deposits are presented by the feldsparic–fluorspar–phenacite–bertrandite metasomatites formed in the carboniferous limestones during their metasomatic alternation with hydrothermal solutions by introducing F, Be, and other associated elements. The formation of early phenacite–fluorspar association occurred in high-fluorite СО2-containing solutions of elevated alkalinity with a salinity of ~10.5%–12% wt eq. NaCl in a temperature range of ~ 370–260 °С at pressures ranging from 1873 to 1248 bar. More recent fluorite and bertrandite deposits were formed by solutions with a salinity of 6.4%–7.7% wt eq. NaCl in a temperature range of ~156 °C–110 °C and a pressure range of 639–427 bar. The examination of the isotopic signature of the ore association minerals confirmed the apocarbonate nature of the main ore deposit and allowed the determination of the magmatogene nature of the ore-forming paleothermal springs, which are the source of subalkaline leucogranites. The primary factors that influenced the formation of the F-Be ore included the reduction of the F activity in solutions because of the binding of Ca and F in fluorite as well as because of the decrease in temperature during the ore deposition process. The elevated alkalinity of the ore-formation solutions resulted in the low solubility of the Be complexes, which caused a relatively low Be content in the ore and a relatively small amount of mineralization in the deposit.


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