Paragenesis of an Orogenic Gold Deposit: New Insights on Mineralizing Processes at the Grass Valley District, California

2020 ◽  
Author(s):  
Ryan D. Taylor ◽  
Thomas Monecke ◽  
T. James Reynolds ◽  
Jochen Monecke

Abstract The Grass Valley orogenic gold district in the Sierra Nevada foothills province, central California, is the largest historical gold producer of the North American Cordillera. Gold mineralization is associated with shallowly dipping north-south veins hosted by the 160 Ma Grass Valley granodiorite to the southwest of the Grass Valley fault and steeply dipping east-west veins in accreted oceanic rocks to the northeast of this major fault. Quartz veins from both vein types show well-preserved primary textural relationships. Using a combination of petrographic and microanalytical techniques, the paragenetic sequence of minerals within the veins and the compositions of ore minerals were determined to constrain the mechanisms of quartz vein formation and gold deposition. The veins are composed of early quartz that formed through cooling of hydrothermal fluids derived from a geopressured reservoir at depth. The early quartz shows growth zoning in optical cathodoluminescence and contains abundant growth bands of primary inclusions. The primary inclusion assemblages and myriads of crosscutting secondary fluid inclusions have been affected by postentrapment modification, suggesting that early quartz formation was postdated by pronounced pressure fluctuations. These pressure fluctuations, presumably involving changes from lithostatic to hydrostatic conditions, may be related to fault failure of the host structure as predicted by the fault-valve model. Fluid flow associated with pressure cycling took place along microfractures and grain boundaries resulting in extensive recrystallization of the early quartz. Deposition of pyrite, arsenopyrite, and first-generation gold from these hydrothermal fluids causing recrystallization of the early quartz occurred as a result of wall-rock sulfidation. The gold forms invisible gold in the compositionally zoned pyrite or micron-sized inclusions within pyrite growth zones. The latest growth zones in euhedral quartz crystals that formed in association with this stage of the paragenesis contain very rare primary fluid inclusions that have not been affected by postentrapment modification. The hydrothermal system transitioned entirely to hydrostatic conditions immediately after formation of the latest quartz, explaining the preservation of the primary fluid inclusions. The formation of minor quartz in open spaces was followed by the deposition of second-generation native gold and telluride minerals that are commonly associated with base metal sulfides. Ore formation at this stage of the paragenesis is attributed to the rapid decompression of hydrothermal fluids escaping from the geopressured part of the crust into the overlying hydrostatic realm. There is no fluid inclusion evidence that this pressure drop resulted in fluid immiscibility of the hydrothermal fluids. Fluid inclusion evidence suggests that the north-south veins formed at a paleodepth of ~8 km, whereas the east-west veins appear to have formed at ~10 to 11 km below surface, confirming previous inferences that the NE-dipping Grass Valley reverse fault accommodated a large displacement. The findings of the study at Grass Valley have significant implications for the model for orogenic gold deposits, as the reconstruction of the paragenetic relationships provides evidence for the occurrence of two discrete events of gold introduction that occurred at different conditions during the evolution of the hydrothermal system.


1989 ◽  
Vol 26 (4) ◽  
pp. 694-715 ◽  
Author(s):  
John F. Slack ◽  
Paul R. Coad

Tourmaline and chlorite are the principal ferromagnesian silicate minerals in the Kidd Creek massive sulphide deposit. Tourmaline is most common in sphalerite-rich peripheral margins of the chalcopyrite stringer zone. Within the north orebody, samples typically contain <1% tourmaline, but small areas (hand-specimen scale) may have 10–20%. Chlorite is more widely distributed and in places constitutes 30–50% of rock volumes. Associated assemblages may include quartz, sulphides (principally chalcopyrite, sphalerite, and (or) pyrite), carbonate, albite, sericite, and rare fluorite, allanite, or zoisite(?).The tourmalines and chlorites record a series of multiple hydrothermal and metamorphic events. Paragenetic studies suggest that tourmaline was deposited during several discrete stages of mineralization, as evidenced by brecciation and cross-cutting relationships. Most of the tourmalines have two concentric growth zones defined by different colours (green, brown, blue, yellow). Some tourmalines also display pale discordant rims that cross-cut and embay the inner growth zones and polycrystalline, multiple-extinction domains. Late sulphide veinlets (chalcopyrite, pyrrhotite) transect the inner growth zones and pale discordant rims of many crystals. The concentric growth zones are interpreted as primary features developed by the main ore-forming hydrothermal system, whereas the discordant rims, polycrystalline domains, and cross-cutting sulphide veinlets reflect post-ore metamorphic processes.Detailed electron microprobe analyses of tourmalines show a wide compositional range, from Fe-rich dravite nearly to end-member schorl, with Fe/(Fe + Mg) ratios varying from 0.33 to 0.92; only minor amounts of Ca are present, yielding uniformly high Na/(Na + Ca) ratios of 0.84–0.99. Two sets of chemical zoning trends are identified in the tourmalines, involving systematic changes in Fe/(Fe + Mg), Na/(Na + Ca), Al, and Ti that are believed to reflect internal coupled substitutions (e.g.,  + Ti = Na + Al) and local mineral equilibria (e.g., tourmaline–chlorite). Analyses of the pale discordant reaction rims show consistent depletion of Fe, Ca, and Ti, presumably by fluid–solid reactions during post-ore metamorphism.Chlorites also show an extensive range in composition, from ripidolite nearly to end-member daphnite, with Fe/(Fe + Mg) ratios of 0.43–0.98 and Si cation values of 5.00–5.39. Chlorites from the fringes of the footwall stringer zone have narrow compositional ranges, whereas chlorites near footwall rhyolite sills in the core of the stringer zone display major variations in Fe/(Fe + Mg) ratios, including one sample with a range of 0.68–0.95. The former group of chlorites has Fe/(Fe + Mg) ratios that correlate well with those of coexisting tourmalines (exclusive of late reaction rims). Data for the latter group, in contrast, fall off equilibrium KD curves, indicating that the tourmalines and chlorites within these samples are not in chemical equilibrium. The chlorites are believed to have been altered (overprinted) by Fe-rich hydrothermal fluids apparently generated during intrusion of the rhyolite sills. The tourmalines, however, are unaffected and retain primary chemical signatures.Variations in mineral proportions and mineral chemistry within the deposit mainly depend on fluctuations in temperature, pH, water/rock ratios, and amounts of entrained seawater. The major proposed control is mixing between high-temperature, Fe-rich end-member hydrothermal fluids and cold, Mg-rich entrained seawater. Fe/(Fe + Mg) variations in footwall tourmalines (and equilibrium chlorites) are believed to largely reflect the progressive infiltration of Mg-rich seawater into the margins and top of the hydrothermal system. The more Fe-rich compositions of Kidd Creek tourmalines relative to those from sediment-hosted massive sulphide deposits (e.g., Sullivan, British Columbia) may be related to the preferential generation of end-member hydrothermal fluids in proximal volcanic environments like that at Kidd Creek.



2020 ◽  
Vol 57 (12) ◽  
pp. 1392-1410 ◽  
Author(s):  
Xi-Heng He ◽  
Xiao-Hua Deng ◽  
Leon Bagas ◽  
Jing Zhang ◽  
Chao Li ◽  
...  

The Xiaorequanzi Cu–Zn deposit is in the westernmost part of East Tianshan Terrane in northwestern China. The deposit is unique in the region being a volcanogenic massive sulphide (VMS) deposit located near a zone (or belt) containing giant late Paleozoic porphyry Cu deposits. Aiming to better understand the genesis of the mineral deposits in the terrane and their tectonic setting, we report our findings of detailed studies on fluid inclusion microthermometry, Re–Os dating of chalcopyrite from the massive ore, and U–Pb dating of zircons from the host volcanic rocks. There are two sulphide stages with early pyrite succeeded by chalcopyrite–sphalerite, which are hydrothermally overprinted and supergene enriched. The hydrothermal overprinting is characterised by quartz–sulphide veins crossed by carbonate-rich quartz veins. Quartz from the chalcopyrite–sphalerite stage is characterised by primary fluid inclusions containing H2O–NaCl(–CO2) and homogenise at 228–392 °C with a salinity of 2.2–13.3 wt.% NaCl equiv. Secondary fluid inclusions related to the hydrothermal overprinting homogenise at 170–205 °C with a salinity of 2.7–12.1 wt.% NaCl equiv. Fluid inclusions in the quartz–sulphide stage of the hydrothermal overprinting contain H2O–NaCl with homogenisation temperatures of 164–281 °C and salinities in ranging from 2.9 to 12.4 wt.% NaCl equiv. Fluid inclusion in the quartz–calcite stage contain H2O–NaCl with homogenisation temperatures of 122–204 °C with salinities of 1.4–12.4 wt.% NaCl equiv. These characteristics are like those of the secondary fluid inclusions in the VMS mineralisation. Combining these findings with H–O isotopic data from previous studies, we propose that the primary mineralising fluid is magmatic in origin. Tuff hosting the mineralisation yields a SHRIMP U–Pb zircon age of 352 ± 5 Ma, which is interpreted as the age of the tuff, and a porphyritic felsite dyke intruding the tuff yields a SHRIMP U–Pb zircon date of 345 ± 6 Ma, interpreted as the emplacement age of the dyke. Chalcopyrite from the main orebody at Xiaorequanzi yields a Re–Os isochron age of 336 ± 13 Ma with an initial 187Os/188Os ratio of 0.25 ± 0.55 (MSWD = 12). Given that the VMS deposit is a syngenetic deposit, we regard the upper ca. 349 Ma limit of the Re–Os date as the approximate age of the chalcopyrite. The three dates are the same within error, and the upper limit of the Re–Os date of ca. 349 is taken as the age of the volcanic, dyke, and mineralisation. The volcanic rocks around the Xiaorequanzi deposit have been previously classified as calc–alkaline to high-K calc–alkaline enriched in large-ion lithophile elements and depleted in high-field-strength elements, which are characteristics indicative of a forearc setting. It is suggested that VMS mineralisation formed in a forearc setting related to the north-directed subduction of the Palaeo-Kangguer or North Tianshan oceanic plates.



Minerals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 240
Author(s):  
Vsevolod Yu. Prokofiev

Fluid inclusions provide valuable information on the composition and physical and chemical parameters of mineral-forming hydrothermal fluids [...]



2006 ◽  
Vol 70 (2) ◽  
pp. 159-173 ◽  
Author(s):  
E.V. Gavrilenko ◽  
B. Calvo Pérez ◽  
R. Castroviejo Bolibar ◽  
D. García del Amo

AbstractThe aim of this study is to provide the first detailed mineralogical and fluid-inclusion description of emeralds from the Delbegetey deposit (Kazakhstan). The characteristic features of Delbegetey emeralds are established: they have dissolution figures on crystal faces, bluish colour and distinct colour zoning; the refractive indices are ω = 1.566–1.570, ε = 1.558–1.562, and the specific gravity is 2.65±0.005, relatively low for natural emeralds; they have very small concentrations of the impurities (Fe, Mg, Na and others) typical of other emeralds, and contain Cr and V; there is a significant preponderance of vapour in fluid inclusions of all types and there is liquid-to-vapour homogenization of primary fluid inclusions (at 395–420°C). The lattice oxygen isotope composition data obtained (δ18O SMOW value of 11.3%o) situate the deposit within the range characteristic of other granite-related emerald deposits. Emerald crystallization took place in low-density (0.40–0.55 g/cm3) aqueous fluid, with the following chemical composition (mol.%): 75.6-97.4 H2O, 0.0-18.4 CO2, 0.0-0.9 CH4, and 4.06-9.65 wt.% NaCl equiv. salinity. According to the calculated isochores, the pressure of formation of the Delbegetey emeralds can be estimated at 570–1240 bar.



Geofluids ◽  
2017 ◽  
Vol 2017 ◽  
pp. 1-25 ◽  
Author(s):  
Matthieu Harlaux ◽  
Julien Mercadier ◽  
Wilédio Marc-Emile Bonzi ◽  
Valentin Kremer ◽  
Christian Marignac ◽  
...  

The Beauvoir granite (Massif Central, France) represents an exceptional case in the European Variscan belt of a peraluminous rare-metal granite crosscutting an early W stockwork. The latter was strongly overprinted by rare-metal magmatic-hydrothermal fluids derived from the Beauvoir granite, resulting in a massive topazification of the quartz-ferberite vein system. This work presents a complete study of primary fluid inclusions hosted in quartz and topaz from the Beauvoir granite and the metasomatized stockwork, in order to characterize the geochemical composition of the magmatic fluids exsolved during the crystallization of this evolved rare-metal peraluminous granite. Microthermometric and Raman spectrometry data show that the earliest fluid (L1) is of high temperature (500 to >600°C), high salinity (17–28 wt.% NaCl eq), and Li-rich (Te<−70°C) with Na/Li ratios ~5. LA-ICPMS analyses of L1-type fluid inclusions reveal that the chemical composition of this magmatic-hydrothermal fluid is dominated by Na, K, Cs, and Rb, with significant concentrations (101–104 ppm) in rare-metals (W, Nb, Ta, Sn, and Li). This study demonstrates that primary fluid inclusions preserved the pristine signature of the magmatic-hydrothermal fluids in the Beauvoir granite but also in the metasomatized W stockwork, despite the distance from the granitic cupola (>100 m) and interaction with external fluids.



1998 ◽  
Vol 62 (3) ◽  
pp. 421-429 ◽  
Author(s):  
C. M. Rice ◽  
K. E. Darke ◽  
J. W. Still ◽  
E. E. Lachowski

AbstractW-bearing rutile formed during alteration of jarosite by resurgent hydrothermal fluids in the oxide zone of the Kori Kollo gold deposit. The rutile shows sector zoning in basal sections and well developed multiple growth zones, both defined in backscatter electron images by variations in the W content. The maximum WO3 content is 5.3 wt.% and W substitutes for Ti with double substitution of Fe to maintain charge balance. The causes of multiple growth bands are considered to be changes in externally controlled variables occurring in a shallow hydrothermal system. Whereas Ti is probably leached from biotite in dacitic rocks, the W is introduced by hydrothermal fluids.



2014 ◽  
Vol 78 (7) ◽  
pp. 1571-1587 ◽  
Author(s):  
E. P. Lynch ◽  
A. Costanzo ◽  
M. Feely ◽  
N. J. F. Blamey ◽  
J. Pironon ◽  
...  

AbstractNew fluid inclusion analyses using a range of analytical techniques including quadropole mass spectrometric analyses coupled with gemmological investigations were conducted on rough and gemquality faceted emeralds from the Piteiras Mine, Minas Gerais, Brazil. These data complement those of Rondeau et al. (2003) who also presented analyses of the Piteiras emeralds. Emeralds are found typically as euhedral-to-anhedral crystals disseminated in biotite-phlogopite schist and range from 0.5 to 50 mm long. Emerald mineralization is associated closely with alkaline metasomatized pegmatite bodies, quartz boudin and veins, and talc-chlorite bands. Four types of fluid inclusions are recognized in the emeralds. These include aqueous brine and aqueous carbonic varieties containing one or two liquid phases, along with gas bubbles and/or solid crystals (e.g. carbonates). Primary fluid inclusions in emeralds record salinities of ~4–24 eq. wt.% NaCl and minimum trapping temperatures from ~350 to 480ºC. Combined microthermometry, Raman spectroscopy and crush-leach gas analyses indicate that the mineralizing fluid was an aqueous carbonic brine enriched in reduced volatile species such as CH4, N2, H2S and alkanes. With respect to their optical properties (RI ε = 1.573–1.580; RI ω = 1.580–1.588; birefringence = 0.006–0.008) and specific gravity (2.65–2.78), the Piteiras emeralds fall within the expected range for metasomatic, schist-hosted emeralds.



2018 ◽  
Vol 5 (9) ◽  
pp. 180260
Author(s):  
Takuya Saito ◽  
Hua-Ning Qiu ◽  
Takazo Shibuya ◽  
Yi-Bing Li ◽  
Kouki Kitajima ◽  
...  

Fluid inclusions in hydrothermal quartz in the 2.4 Ga Ongeluk Formation, South Africa, are expected to partially retain a component of the ancient seawater. To constrain the origin of the fluid and the quartz precipitation age, we conducted Ar–Ar dating for the quartz via a stepwise crushing method. The obtained argon isotopes show two or three endmembers with one or two binary mixing lines as the crushing proceeds, suggesting that the isotopic compositions of these endmembers correspond to fluid inclusions of each generation, earlier generated smaller 40 Ar- and K-rich inclusions, moderate 40 Ar- and 38 Ar Cl (neutron-induced 38 Ar from Cl)-rich inclusions and later generated larger atmospheric-rich inclusions. The K-rich inclusions show significantly different 40 Ar/ 38 Ar Cl values compared to the 38 Ar Cl -rich inclusions, indicating that it is difficult to constrain the quartz formation age using only fluid inclusions containing excess 40 Ar. The highest obtained 40 Ar/ 36 Ar value from the fluid inclusions is consistent with an expected value of the Ongeluk plume source, suggesting that the quartz precipitation was driven by Ongeluk volcanism. Considering the fluid inclusion generations and their compositions, the hydrothermal system was composed of crustal fluid and magmatic fluid without seawater before the beginning of a small amount of seawater input to the hydrothermal system.



2014 ◽  
Vol 962-965 ◽  
pp. 41-44
Author(s):  
Hao Wei ◽  
Jiu Hua Xu ◽  
Guo Rui Zhang

In this paper we use new field data, fluid inclummsions, and table isotopes (O, H, and S) to refine the roles of the hydrothermal evolution, evaluate changes in the hydrothermal fluids of Duobaoshan porphyry Cu (Mo) deposit and Sankuanggou skarn Fe-Cu deposit. Four ore-forming stages are recognized at The Duobaoshan porphyry Cu (Mo) deposit. Fluid inclusions are abundant in quartz of various stages. Estimated trapping pressures for stage I, II, III are 110-160MPa, 58-80MPa, and 8-17MPa, corresponding trapping temperatures are 375-650°C, 310-350°C, 210-290°C. The δD and δ18O values of fluids indicate a evolution process from magmtic hydrothermal fluid to a mixing magmtic and meteoric fluid. The δ34S values of sulfides mainly suggest predominantly source of deep magma chamber.



1990 ◽  
Vol 54 (375) ◽  
pp. 305-309 ◽  
Author(s):  
A. Canals-Sabate ◽  
J. C. Touray ◽  
J. Fabre

AbstractLarge thenardite crystals have been sampled at New Agorgott, in the Taoudenni area of northern Mali. They are still in equilibrium with a pressurized NaCl saturated brine capped by a halite layer. Clays located about 1 m above the thenardite occurrence have been dated at 6760 y.BP. The crystals contain numerous, large, brine and solid inclusions. Microcryscopic studies show that the fluids can be explained by the addition of MgCl2 to the Na2SO4-NaCl-H2O system (eutectic temperature: −31 to −35°C; possible bloedite Na2Mg(SO4)2.4H2O formed after freezing). The homogenization temperatures of primary fluid inclusions are in the range 28 to 50°C. In order to understand the significance of the highest Th values, overheating experiments under 1 bar pressure were performed at different heating rates up to 170°C. The results are as follows:(i)When the temperature of stretching (TOh) is higher than about 10°C, overheating is recorded and fossilized (identical Th after some hours, several days or 8 months storage at 5°C).(ii)The lowest Th values (28°C) are probably near the formation temperature of thenardite; the highest ones reflect stretching under present desert conditions.(iii)With TOh lower than about 60°C, a fair correlation is observed between Th and TOh.Finally, taking into account recent natural overheating, the fluid inclusion data are compatible with the formation of thenardite from underground brines later than the beginning of desert conditions in the Taoudenni area (i.e. about 3000 y.BP).



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