Multiple hydrothermal and metamorphic events in the Kidd Creek volcanogenic massive sulphide deposit, Timmins, Ontario: evidence from tourmalines and chlorites

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.


1991 ◽  
Vol 28 (12) ◽  
pp. 1887-1904 ◽  
Author(s):  
Jacques Trottier ◽  
Alex C. Brown ◽  
Michel Gauthier

The Memphremagog polymetallic massive sulphide deposit occurs at the contact between a pillowed volcanic sequence and a detrital sedimentary sequence consisting principally of shale and greywacke. The deposit, situated about 100 km east of Montréal in the Appalachians of southeastern Quebec, is composed of massive sulphide breccia. Major minerals include pyrrhotite, pyrite, sphalerite, galena, chalcopyrite, and calcite, with minor amounts of arsenopyrite, freibergite ((Cu,Ag,Fe)12Sb4S13), meneghinite (CuPb13Sb7S24), gudmundite (FeSbS), and kersteritic stannite (Cu2(Fe,Zn)SnS4). The mineral assemblage, metal content, and primary textures are comparable to modern sea-floor sulphide mounds enclosed by thick sedimentary sequences deposited in basins such as the Guaymas Basin in the Gulf of California.Although the footwall basalt unit is interstratified with the St-Daniel Formation of the Ophiolite Belt, it possesses a transitional geochemical signature of alkaline affinity that is uncharacteristic of ophiolitic basalts. We propose that this volcanic unit was emplaced within a transtensional basin of a rifted fore-arc system that formed during the Taconic orogeny as a result of diachronous oblique collision of an island- arc system (Ascot–Weedon?) with the North American continent. During magmatic activity, a hydrothermal system was imprinted on the volcanics and underlying sediments. Subsequent hydrothermal fluid emanations led to the formation of the Memphremagog sulphide deposit, which is quite distinct from sulphide deposits generally found within ophiolite belts.



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.







2016 ◽  
Vol 53 (12) ◽  
pp. 1458-1475
Author(s):  
Patrick J. Sack ◽  
Ron F. Berry ◽  
J. Bruce Gemmell ◽  
Sebastien Meffre ◽  
Andrew West

This paper presents results of a laser ablation – inductively coupled plasma – quadrapole mass spectrometer (LA–ICP–QMS) U–Pb dating study of small in situ zircon grains from samples collected in the vicinity of the Greens Creek massive sulphide deposit, on northern Admiralty Island, southeast Alaska. The Greens Creek mine is a volcanogenic massive sulphide deposit in the central portion of the Alexander Triassic metallogenic belt (ATMB) and is one of the top global silver producers despite having a dominantly mafic metavolcanic stratigraphic footwall. The stratigraphic footwall is a Mississippian mafic metavolcanic sequence with a protolith age of approximately 340–330 Ma. The first U–Pb zircon constrained chronostratigraphy for the area places the deposit near, or at, the base of the host Late Triassic stratigraphy just above an approximately 100 million year old unconformity and probably 10–15 million years older than mineralization at the Palmer and Windy Craggy deposits in the northern portion of the ATMB. The stratigraphic location of the Greens Creek deposit is atypical for a syngenetic massive sulphide deposit, and this may, at least partly, explain its unusual metal endowment. Pre-mineralization Permian U–Pb zircon metamorphic ages are consistent with published 273–260 Ma white mica ages related to the collision of the Admiralty and Craig subterranes, the basement to the ATMB. The much older age of the footwall rocks and their Permian pre-mineralization metamorphism demonstrates that though the mafic volcanic rocks are not genetically linked to the deposit, they likely influenced the style of alteration and mineralization.



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