The Formation of Magmatic-Hydrothermal Features in Sn-Mineralized and Barren Tasmanian Intrusions, Southeast Australia: Insights from Quartz Textures, Trace Elements, and Microthermometry

2021 ◽  
Vol 116 (8) ◽  
pp. 1917-1948
Author(s):  
Wei Hong ◽  
David R. Cooke ◽  
Lejun Zhang ◽  
Nathan Fox ◽  
Jay Thompson

Abstract Tasmania is the most important tin province in Australia, having been endowed with >0.65 Mt Sn. Some granitic intrusions in western Tasmania have distinctive tourmaline- and quartz-rich magmatic-hydrothermal features, whether they are mineralized (e.g., Heemskirk Granite) or barren (Pieman Heads Granite). The Devonian Heemskirk and Pieman Heads plutons crop out on the western coast of Tasmania and are characterized by similar mineralogical and geochemical compositions and ages. The magmatic-hydrothermal textural features include tourmaline patches, tourmaline orbicules, and tourmaline-muscovite veins, as well as miarolitic cavities and quartz-fluorite-sulfide veins in the Heemskirk Granite. Cathodoluminescence (CL) imaging, laser ablation-inductively coupled plasma-mass spectrometry, and microthermometric analyses of quartz have revealed the physicochemical evolution of the magmatic-hydrothermal fluids from which these tourmaline- and quartz-bearing assemblages precipitated. High Ti quartz (20–28 ppm) in tourmaline patches, orbicules, and cavities typically have homogeneous CL-bright intensity, whereas CL-dark fractures have cut and/or offset the CL-bright and -gray domains that characterize low Ti quartz (3.4–8.5 ppm) from the tourmaline veins. The earliest fluid inclusion assemblages in the quartz-tourmaline orbicules and cavities have a salinity range from 3 to 14 wt % NaCl equiv with intermediate density and were probably trapped at lithostatic pressures of 1.57 ± 0.2 kbar and temperatures of 550° to 570°C, suggesting a depth of 5.9 ± 0.8 km. Prolonged depressurization and cooling may have led to the evolution of a brine (~39 wt % NaCl equiv salinity) from the primary magmatic liquid, which formed halite-bearing hypersaline inclusions in the tourmaline orbicules. Continuous pressure decrease explains the intense brittle failure and fluid migration outward from the apical portions of the pluton, where magmatic fluids partially mixed with and were cooled by external meteoric water. These mechanisms triggered the formation of tourmaline-muscovite-quartz veins and local cassiterite-bearing greisens from a moderate-salinity fluid (~12 wt % NaCl equiv) at temperatures of ~300°C and hydrostatic pressures of 120 bars. Retrograde dissolution textures evident from CL-bright quartz cores surrounded by oscillatory growth zones with gray CL response characterize the low Ti (<1 ppm) and high Al (500–1,000 ppm) quartz from the fluorite-sulfide veins that precipitated from a low-salinity (5.7 wt % NaCl equiv) acidic fluid at temperatures of 200° ± 25°C and hydrostatic pressures of <50 bars. High Sb concentrations (up to 80 ppm) in quartz may be an indicator of low-temperature base metal mineralization related to granitic intrusions. Abundant fluid percolation, protracted fractional crystallization, and high tin concentrations in exsolved hydrothermal fluids may explain why the Heemskirk Granite is well endowed in Sn and base metal deposits, whereas the Pieman Heads Granite is barren.

2020 ◽  
Vol 81 (3) ◽  
pp. 102-104
Author(s):  
Milen Stavrev ◽  
Robert Creaser ◽  
Irena Peytcheva ◽  
Atanas Hikov ◽  
Silvia Chavdarova

The study presents first Re-Os age data of molybdenite from the region at Babyak Mo-Ag-Au-W-Bi-base metal deposit, in combination with electron microprobe and laser ablation inductively coupled plasma mass spectrometry results for molybdenite aggregates. The Re-Os geochronology of the analyzed samples defines age at 52.6 ± 0.2 to 53 ± 0.2 Ma of the ore-forming process in the Babyak area. It marks a distinct fertile Early Eocene event in the Cretaceous-Paleogene evolution of the Rila-West Rhodopes batholith.


Author(s):  
Donnelly B. Archibald ◽  
Lauren M.G. Macquarrie ◽  
J. Brendan Murphy ◽  
Robin A. Strachan ◽  
Chris R.M. McFarlane ◽  
...  

Magmatic and tectonic processes can transport large volumes of magma generated in the deep crust as discrete pulses to shallower crustal depths, resulting in the incremental construction of large, composite batholiths over thousands to tens of millions of years. The Silurian to Early Devonian Donegal composite batholith in Ireland is a classic example of which regional geological syntheses and lithogeochemical data show that emplacement was syn- and post-kinematic with respect to the terminal phases (ca. 437−415 Ma) of the Caledonian orogeny. We used U-Pb dating of zircon and titanite to investigate the construction of the batholith over time. Imaging of these minerals reveals complex, zoned grains with distinct autocrystic (growth during pluton emplacement) and antecrystic (growth during lower crustal incubation) domains as well as xenocrysts (incorporated from wall rocks). To determine the ages of emplacement and of inherited domains, discrete growth zones were targeted for dating using laser ablation−inductively coupled plasma−mass spectrometry (LA-ICP-MS). Taken together, the zircon and titanite U-Pb isotopic data indicate that magmatism occurred over at least 30 m.y., between ca. 430 Ma and 400 Ma. Batholith emplacement is bracketed by the ca. 427−423 Ma Ardara pluton and the latest phases in the Main Donegal and Trawenagh Bay plutons (ca. 400 Ma). Although apparently volumetrically minor, U-Pb data from spatially associated mafic rocks (appinite suite, lamprophyre dikes, and mafic enclaves in granitoid plutons) yield ages ranging from ca. 431−416 Ma, which indicates ongoing mafic magmatism during emplacement of much of the Donegal composite batholith.


Clay Minerals ◽  
2018 ◽  
Vol 53 (2) ◽  
pp. 289-303
Author(s):  
Işil Ömeroğlu Sayit ◽  
Asuman Günal Türkmenoğlu ◽  
Ş. Ali Sayin ◽  
Cengiz Demirci

ABSTRACTThe mineralogy, texture and composition of rocks associated with the kaolin deposits in the Ahırözü-Hamidiye-Üçbaşlı area, SE of Mihalıççık, Eskişehir, Turkey, were investigated. In the study area, Triassic, blue-green schists and serpentinized ultramafic rocks are exposed. Kaolinization occurs at the contact between a Triassic granitic intrusion and metamorphic rocks. Textural and mineralogical characteristics were identified by X-ray diffraction (XRD) and scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX) analyses. The effects of hydrothermal alteration on the whole-rock chemical composition were determined by inductively coupled plasma mass spectrometry (ICP-MS) analysis. Homogenization temperature (Th, °C), salinity, (wt.% NaCl) and melting temperature (Tm, °C) were detected by fluid-inclusion analyses.The argillic alteration zone (Zone A) includes kaolinite, smectite, natroalunite and accessory pyrite, hematite and goethite. This paragenesis corresponds to a low–intermediate argillic alteration caused by fluids having neutral to acidic pH, at a temperature of <200°C. The propylitic alteration zone (Zone B) is characterized by epidote, chlorite, illite and pyrite and was caused by fluids with a neutral pH and a temperature of >250°C. The rocks in Zone C are mainly silicified and represent sinter formation in the study area. The rocks in the kaolin deposit are depleted in Rb, Pb and Y and enriched in Cs, U and Sr, and represent the products of epithermal hydrothermal alteration of granitic intrusions emplaced in a volcanic arc.


Author(s):  
Mizuki Ishida ◽  
Rurik Romero ◽  
Mathieu Leisen ◽  
Kazutaka Yasukawa ◽  
Kentaro Nakamura ◽  
...  

AbstractPyrite geochemistry has proven useful for tracking changes in the composition and physico-chemical conditions of hydrothermal fluids in ore-forming environments. Here, we investigated the microtextural features and chemical composition of pyrite, a main Au-bearing phase in the Akeshi and Kasuga deposits (Southern Kyushu, Japan), to better constrain the ore-forming processes in these high-sulfidation epithermal Au deposits. Despite the widespread distribution of Au-bearing pyrite in both deposits, no visible Au minerals coexist with pyrite. However, in situ laser ablation inductively coupled plasma mass spectrometry results show that Au concentrations in pyrite vary from below the detection limit to 41 ppm and are positively correlated with Cu (r = 0.4; up to 7400 ppm) and Bi concentrations (r = 0.44; up to 640 ppm). In both deposits, high Cu and Au concentrations occur in small (< 25 μm) anhedral grains of pyrite, which are interpreted to have rapidly crystallized from the ore-forming hydrothermal fluid. In addition, dissolution–reprecipitation textures and thin, concentric, Cu-rich overgrowths were identified in a number of larger (> 25 μm) pyrite grains and aggregates. These abrupt changes in the trace element compositions of pyrite grains likely record episodic metal-rich fluid inputs. We also propose that gold adsorption onto growing pyrite surfaces played a key role in the mineralization of these deposits.


2020 ◽  
Author(s):  
Daniel Bůžek ◽  
Slavomír Adamec ◽  
Kamil Lang ◽  
Jan Demel

<div><p>UiO-66 is a zirconium-based metal-organic framework (MOF) that has numerous applications. Our group recently determined that UiO-66 is not as inert in aqueous dispersions as previously reported in the literature. The present work therefore assessed the behaviour of UiO-66 in buffers: 2-amino-2-(hydroxymethyl)-1,3-propanediol (TRIS), 4-(2-hydroxyethyl)piperazine-1-ethane sulfonic acid (HEPES), N-ethylmorpholine (NEM) and phosphate buffer (PB), all of which are commonly used in many UiO-66 applications. High pressure liquid chromatography and inductively coupled plasma mass spectrometry were used to monitor degradation of the MOF. In each buffer, the terephthalate linker was released to some extent, with a more pronounced leaching effect in the saline forms of these buffers. The HEPES buffer was found to be the most benign, whereas NEM and PB should be avoided at any concentration as they were shown to rapidly degrade the UiO-66 framework. Low concentration TRIS buffers are also recommended, although these offer minimal buffer capacity to adjust pH. Regardless of the buffer used, rapid terephthalate release was observed, indicating that the UiO-66 was attacked immediately after mixing with the buffer. In addition, the dissolution of zirconium, observed in some cases, intensified the UiO-66 decomposition process. These results demonstrate that sensitive analytical techniques have to be used to monitor the release of MOF components so as to quantify the stabilities of these materials in liquid environments.</p></div>


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