Magmatic Origin for Sediment-Hosted Au Deposits, Guizhou Province, China: In Situ Chemistry and Sulfur Isotope Composition of Pyrites, Shuiyindong and Jinfeng Deposits

2018 ◽  
Vol 113 (7) ◽  
pp. 1627-1652 ◽  
Author(s):  
Zhuojun Xie ◽  
Yong Xia ◽  
Jean S. Cline ◽  
Michael J. Pribil ◽  
Alan Koenig ◽  
...  

Abstract The southwest Guizhou Province, China, contains numerous sediment-hosted Au deposits with Au reserves greater than 700 tonnes. To date, the source of ore fluids that formed the Guizhou sediment-hosted Au deposits is controversial, hampering the formulation of genetic models. In this study, we selected the Shuiyindong and Jinfeng Au deposits, the largest strata-bound and fault-controlled deposits in Guizhou, respectively, for detailed research on pyrite chemistry and S isotope composition using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) and laser ablation-multicollector-inductively coupled plasma-mass spectrometry (LA-MC-ICP-MS), respectively. Petrography and pyrite chemistry studies distinguished five generations of pyrite. Among these, pre-ore pyrite 2 and ore pyrite are the most abundant types in the deposits. Pre-ore pyrite 2 is anhedral to euhedral and with ~2,639 ppm As and wider ranges of Cu, Sb, and Pb (<~22–4,837 ppm, <~6 to 532 ppm, and <~4 to 1,344 ppm, respectively). Gold in pre-ore pyrite 2 is below the detection limit of LA-ICP-MS (~2 ppm). Pre-ore pyrite 2 is interpreted to have a sedimentary (syngenetic or diagenetic) origin. Ore pyrite commonly rims the four identified pre-ore pyrites or occurs as individual, anhedral to euhedral crystals. Ore pyrite is enriched in Au (~641 ppm), As (~9,147 ppm), Cu (~1,043 ppm), Sb (~188 ppm), Hg (~43 ppm), and Tl (~22 ppm) in both deposits. Ore pyrite formed mainly by sulfidation of Fe in Fe-bearing host rocks, mainly Fe dolomite, and As, Cu, Sb, Hg, and Tl, also in ore fluids, were incorporated into ore pyrite. In situ δ34S isotope ratios for pre-ore pyrite 2 and ore pyrite were measured by LA-MC-ICP-MS. Pre-ore pyrite 2 from Shuiyindong and Jinfeng deposits resulted in δ34S values ranging from −0.8 to +3.4‰ and from 5.1 to 10.5‰, respectively. Analyses of ore pyrite from the Shuiyindong have δ34S values that vary from −3.3 to +2.5‰, with a median of 0.7‰; analyses of ore pyrite from the Jinfeng range from 8.9 to 11.2‰, with a median at 10.3‰. Available bulk and in situ δ34S data in the literature for pre-ore pyrites 1 and 2 and ore-related sulfide minerals including ore pyrite, arsenopyrite, and late ore-stage stibnite, realgar, orpiment, and cinnabar from several Guizhou sediment-hosted Au deposits were compiled for comparison. Pre-ore-stage pyrites from Guizhou sediment-hosted Au deposits have a broad range of δ34S values, from −33.8 to + 17.9‰ (including in situ and available bulk δ34S data). Ore-related sulfide minerals in all Guizhou sediment-hosted Au deposits, except Jinfeng, have very similar δ34S values, and most data plot between ~−5 and +5‰. In the Jinfeng deposit, the ore-related sulfide minerals exhibit δ34S values ranging from 1.9 to 18.1‰, with most data plotting between 6 and 12‰. The broad range of S isotope compositions for the sedimentary pyrites (pre-ore pyrites 1 and 2) indicate that S in these pre-ore pyrites was most likely generated by bacterial reduction from marine sulfate. The narrow range of δ34S values (~−5–+5‰) for ore-related sulfide minerals in all Guizhou sediment-hosted Au deposits, excepting the Jinfeng deposit, suggests that the deposits may have formed in response to a single widespread metallogenic event. As the S isotope fractionation between hydrothermal fluids and sulfide minerals in a sulfide-dominated system is small (<2‰) at ~250°C, the initial ore fluids that formed the Guizhou sediment-hosted Au deposits would have had δ34S values similar to the ore-related sulfide minerals, between ~−5 and +5‰. At Jinfeng, initial ore fluids may have mixed with local fluids with heavier δ34S, possibly basin brine (δ34Sbasin brine >18‰), resulting in elevated δ34S values of ore-related sulfide minerals and especially late ore-stage sulfide minerals. Although few igneous rocks are exposed in the mining area around these deposits, there is evidence of magmatic activity ~20 km away. Furthermore, gravity and magnetic geophysical investigations indicate the presence of a pluton ~5 km below the surface of the Shuiyindong district. Based on in situ S isotope results and recent data indicating proximal intrusions, we interpret a deep magmatic S source for the ore fluids that formed the Guizhou sediment-hosted Au deposits. However, as the age for Au mineralization of Guizhou sediment-hosted Au deposits is still debated, the mineralization-magma connection remains hypothetical. Identifying an ore fluid source and time frame for Guizhou Au mineralization continues to be a critically important research goal for this district.

2019 ◽  
Vol 34 (9) ◽  
pp. 1800-1809 ◽  
Author(s):  
Wen Zhang ◽  
Zaicong Wang ◽  
Frédéric Moynier ◽  
Edward Inglis ◽  
Shengyu Tian ◽  
...  

An in situ Zr isotopic analytical method for zircons was developed using LA-MC-ICP-MS to reveal the Zr stable isotope variation in the complex mineral crystallization history.


2019 ◽  
Vol 34 (8) ◽  
pp. 1546-1552 ◽  
Author(s):  
Lü-Yun Zhu ◽  
Yong-Sheng Liu ◽  
Shao-Yong Jiang ◽  
Jie Lin

The 187Os/188Os ratio in low-Os sulfides could be in situ measured precisely by LA-MC-ICP-MS equipping an array of ion counters.


2020 ◽  
Vol 35 (3) ◽  
pp. 510-517
Author(s):  
Chao Huang ◽  
Yue-Heng Yang ◽  
Lie-Wen Xie ◽  
Shi-Tou Wu ◽  
Hao Wang ◽  
...  

In the present work, we describe a sequential U–Pb and Sm–Nd systematics measurement from natural LREE-enriched minerals using Neptune Plus MC-ICP-MS coupled with a 193 nm excimer laser in a single shot.


2006 ◽  
Vol 10 ◽  
pp. 25-28 ◽  
Author(s):  
Dirk Frei ◽  
Julie A. Hollis ◽  
Axel Gerdes ◽  
Dan Harlov ◽  
Christine Karlsson ◽  
...  

Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) was developed in 1985 and the first commercial laser ablation systems were introduced in the mid 1990s. Since then, LA-ICP-MS has become an important analytical tool in the earth sciences. Initially, the main interest for geologists was in its ability to quantitatively determine the contents of a wide range of elements in many minerals at very low concentrations (a few ppm and below) with relatively high spatial resolution (spot diameters of typically 30–100 μm). The potential of LA-ICP-MS for rapid in situ U–Th–Pb geochronology was already realised in the early to mid 1990s. However, the full potential of LA-ICP-MS as the low-cost alternative to ion-microprobe techniques for highly precise and accurate in situ U–Th–Pb age dating was not realised until the relatively recent advances in laser technologies and the introduction of magnetic sectorfield ICP-MS (SF-ICPMS) instruments. In March 2005, the Geological Survey of Denmark and Greenland (GEUS) commissioned a new laser ablation magnetic sectorfield inductively coupled plasma mass spectrometry (LA-SF-ICP-MS) facility employing a ThermoFinnigan Element2 high resolution magnetic sectorfield ICP-MS and a Merchantek New Wave 213 nm UV laser ablation system. The new GEUS LA-SF-ICP-MS facility is widely used on Survey research projects in Denmark and Greenland, as well as in collaborative research and contract projects conducted with partners from academia and industry worldwide. Here, we present examples from some of the these ongoing studies that highlight the application of the new facility for advanced geochronological and trace element in situ microanalysis of geomaterials. The application of LASF-ICP-MS based in situ zircon geochronology to regional studies addressing the Archaean geology of southern West Greenland is presented by Hollis et al. (2006, this volume).


Geochronology ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 123-147
Author(s):  
Veronica Peverelli ◽  
Tanya Ewing ◽  
Daniela Rubatto ◽  
Martin Wille ◽  
Alfons Berger ◽  
...  

Abstract. Epidote – here defined as minerals belonging to the epidote–clinozoisite solid solution – is a low-μ (μ=238U/204Pb) mineral occurring in a variety of geological environments and participating in many metamorphic reactions that is stable throughout a wide range of pressure–temperature conditions. Despite containing fair amounts of U, its use as a U−Pb geochronometer has been hindered by the commonly high contents of initial Pb, with isotopic compositions that cannot be assumed a priori. We present a U−Pb geochronology of hydrothermal-vein epidote spanning a wide range of Pb (3.9–190 µg g−1), Th (0.01–38 µg g−1), and U (2.6–530 µg g−1) contents and with μ values between 7 and 510 from the Albula area (eastern Swiss Alps), from the Grimsel area (central Swiss Alps), and from the Heyuan fault (Guangdong Province, China). The investigated epidote samples show appreciable fractions of initial Pb contents (f206=0.7–1.0) – i.e., relative to radiogenic Pb – that vary to different extents. A protocol has been developed for in situ U−Pb dating of epidote by spot-analysis laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) with a magmatic allanite as the primary reference material. The suitability of the protocol and the reliability of the measured isotopic ratios have been ascertained by independent measurements of 238U/206Pb and 207Pb/206Pb ratios, respectively, with quadrupole and multicollector ICP-MS applied to epidote micro-separates digested and diluted in acids. For age calculation, we used the Tera–Wasserburg (207Pb/206Pb versus 238U/206Pb) diagram, which does not require corrections for initial Pb and provides the initial 207Pb/206Pb ratio. Petrographic and microstructural data indicate that the calculated ages date the crystallization of vein epidote from a hydrothermal fluid and that the U−Pb system was not reset to younger ages by later events. Vein epidote from the Albula area formed in the Paleocene (62.7±3.0 Ma) and is related to Alpine greenschist-facies metamorphism. The Miocene (19.2±4.3 and 16.9±3.7 Ma) epidote veins from the Grimsel area formed during the Handegg deformation phase (22–17 Ma) of the Alpine evolution of the Aar Massif. Identical initial 207Pb/206Pb ratios reveal homogeneity in Pb isotopic compositions of the fluid across ca. 100 m. Vein epidote from the Heyuan fault is Cretaceous in age ( 107.2±8.9 Ma) and formed during the early movements of the fault. In situ U−Pb analyses of epidote returned reliable ages of otherwise undatable epidote–quartz veins. The Tera–Wasserburg approach has proven pivotal for in situ U−Pb dating of epidote, and the decisive aspect for low age uncertainties is the variability in intra-sample initial Pb fractions.


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