scholarly journals Reconstruction of Hydrothermal Processes in the Cyprus Type Fe-Cu-Zn Deposits of the Italian Northern Apennines: Results of Combined Fluid Inclusion Microthermometry, SEM-CL Imaging and Trace Element Analyses by LA-ICP-MS

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 165
Author(s):  
Gabriella B. Kiss ◽  
Zsolt Bendő ◽  
Giorgio Garuti ◽  
Federica Zaccarini ◽  
Edit Király ◽  
...  
Keyword(s):  
Fluid Inclusion ◽  
Trace Element ◽  
Fluid Inclusions ◽  
Massive Sulfide ◽  
Hydrothermal Activity ◽  
Hydrothermal Systems ◽  
Original Position ◽  
Volcanogenic Massive Sulfide ◽  
Hydrothermal Conditions ◽  
Icp Ms

Quartz from the stockwork zone of various Cyprus type volcanogenic massive sulfide deposits (Boccassuolo, Reppia, Campegli, Bargone and Vigonzano) from the unmetamorphosed, Jurassic Northern Apennine ophiolites was studied in order to provide details on the submarine hydrothermal conditions and the characteristics for ore formation. Our detailed SEM-CL investigation of quartz contributed to a robust characterization and interpretation of primary fluid inclusions and microthermometry data. SEM-CL imaging was also useful for reconstructing the consecutive steps of quartz precipitation. The determination of trace element contents according to growth zoning in quartz by LA-ICP-MS constrained the compositional variations of parent fluids during the hydrothermal activity. A continuously cooling fluid regime characterized each studied volcanogenic massive sulfide (VMS) occurrence although the minimum formation temperatures were different (Bargone: 110–270 °C; Boccassuolo: 60–360 °C; Campegli: 110–225 °C; Reppia: 50–205 °C; Vigonzano: 260–330 °C), the range of temperature most probably depends on the original position of sampling in relation to the centers of the hydrothermal systems. Compositional changes are reflected by variations in the methane content (0.13–0.33 mol/kg) and salinity (2.6–9.3 NaCl equiv. wt. %) in the fluid inclusions of quartz and calcite as well as a changeable Al content (11–1526 ppm) in quartz. This study demonstrates that the combined use of SEM-CL imaging and LA-ICP-MS analyses, coupled with fluid inclusion microthermometry, can constrain the different fluid conditions of ore forming and the barren stages of evolving submarine hydrothermal systems.

Development of a laser ablation ICP-MS method for the analysis of fluid inclusions associated with volcanogenic massive sulfide deposits

2021 ◽  
pp. geochem2020-043
Author(s):  
Madison A. Schmidt ◽  
Matthew I. Leybourne ◽  
Jan M. Peter ◽  
Duane C. Petts ◽  
Simon E. Jackson ◽  
...  
Keyword(s):  
Laser Ablation ◽  
Fluid Inclusions ◽  
Inductively Coupled Plasma ◽  
Massive Sulfide ◽  
Ore Deposits ◽  
Volcanogenic Massive Sulfide ◽  
Metals And Metalloids ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Vms Deposits

There is increasing acceptance of the presence of variable magmatic contributions to the mineralizing fluids in the formation of volcanogenic massive sulfide (VMS) deposits. The world-class Windy Craggy Cu-Co-Au deposit (>300 MT @ 2.12 wt.% Cu) in northwestern British Columbia is of interest because, unlike most VMS deposits, quarts fluid inclusions from within the deposit range from relatively low to intermediate salinity (most 6-16 wt.% equivalent). In this study we used an excimer (193 nm) laser ablation system interfaced to a quadrupole inductively coupled plasma mass spectrometer to quantify key metals and metalloids that are considered by many to be indicative of magmatic contributions to hydrothermal ore deposits. Although LA-ICP-MS signals from these low-salinity inclusions are highly transient, we were able to quantify Na, Mg, K, Ca, Mn, Fe, Co, Cu, Zn, Sr, Sn, Ba, Ce, Pb and Bi consistently – of the 34 elements that were monitored. Furthermore, Cl, Sb, Cd, Mo, Rb, Br, and As were also measured in a significant number of inclusions. Comparison of the fluid inclusion chemistry with unaltered and altered mafic volcanic and sedimentary rocks and mineralized samples from the deposit indicate that enrichment in the main ore metals (Cu, Zn, Fe, Pb) in the inclusions reflects that of the altered rocks and sulfides. Metals and metalloids that may indicate a magmatic contribution typically show much greater enrichments in the fluid inclusions much greater over the host rocks at the same Cu concentration; in particular Bi, Sn and Sb are significantly elevated when compared to the host rock samples. These data are consistent with the ore-forming fluids at Windy Craggy having a strong magmatic contribution.

scholarly journals Subcritical Phase Separation and Occurrence of Deep-Seated Brines at the NW Caldera Vent Field, Brothers Volcano: Evidence from Fluid Inclusions in Hydrothermal Precipitates

Geofluids ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-22
Author(s):  
Alexander Diehl ◽  
Cornel E. J. de Ronde ◽  
Wolfgang Bach
Keyword(s):  
Phase Separation ◽  
Fluid Inclusion ◽  
Fluid Inclusions ◽  
Hydrothermal Vents ◽  
Massive Sulfide ◽  
Growth Conditions ◽  
Hydrothermal Systems ◽  
Small Subset ◽  
Large Area ◽  
Black Smoker

The northwestern caldera wall of Brothers volcano in the southern Kermadec arc features several clusters of hydrothermal venting in a large area that extends from near the caldera floor (~1700 mbsl) almost up to the crater rim (~1300 mbsl). Abundant black smoker-type hydrothermal chimneys and exposed stockwork mineralization in this area provide an excellent archive of hydrothermal processes that form seafloor massive sulfide deposits. Using sulfate precipitates from chimneys and stockwork recently recovered by remotely operated vehicles, we conducted fluid inclusion microthermometry and Sr isotope studies to determine the role of phase separation and mixing between vent fluid and seawater. The variability in the vast majority of fluid inclusion salinities (i.e., 0.1–5.25 wt.% NaCl eq.) and entrapment temperatures of up to 346°C are indicative of phase-separated hydrothermal fluids. Large salinity variations in samples with entrapment temperatures mostly below the boiling temperature for the sample’s depth show that the majority of fluids ascending below the NW Caldera are phase separating in the subsurface and cooling, prior to discharge. In several samples, entrapment temperatures of over 343°C suggest that phase-separating fluids have at least sporadically exited the seafloor at the NW Caldera site. Isobaric-isenthalpic mixing trends between coexisting phase-separated vapors and brines with seawater are consistent with phase-separated fluids at near-seafloor pressures of ~170 bar and suggest that the vast majority of the ascending fluids continue to phase separate to within tens to hundreds of meters below seafloor prior to mixing with seawater. A small subset of the most saline fluid inclusions (up to 18.6 wt.% NaCl eq.) is unlikely formed by near-seafloor phase separation and is considered to be produced either by supercritical phase separation or by the contribution of a magmatic brine from near the magmatic-hydrothermal interface. 87Sr/86Sr values of sulfate samples range from 0.7049 (i.e., near hydrothermal end-member) to 0.7090 (i.e., near seawater) and show that the crystals grew from vapor- and brine-derived fluids in a hydrothermally dominated mixing regime. Our work provides new insights into mineral growth conditions, mixing regimes, and in particular, the extent and character of subseafloor phase separation during the formation of hydrothermal vents and their underlying stockwork in seawater-dominated, arc-related hydrothermal systems.

Quartz precipitation and fluid inclusion characteristics in sub-seafloor hydrothermal systems associated with volcanogenic massive sulfide deposits

2012 ◽  
Vol 4 (2) ◽  
Author(s):  
Matthew Steele-MacInnis ◽  
Liang Han ◽  
Robert Lowell ◽  
J. Rimstidt ◽  
Robert Bodnar
Keyword(s):  
Fluid Inclusion ◽  
Fluid Inclusions ◽  
Hydrothermal System ◽  
Massive Sulfide ◽  
Hydrothermal Systems ◽  
Fluid Immiscibility ◽  
Quartz Dissolution ◽  
Vms Deposits ◽  
Quartz Solubility ◽  
Dissolution And Precipitation

AbstractResults of a numerical modeling study of quartz dissolution and precipitation in a sub-seafloor hydrothermal system have been used to predict where in the system quartz could be deposited and potentially trap fluid inclusions. The spatial distribution of zones of quartz dissolution and precipitation is complex, owing to the fact that quartz solubility depends on many inter-related factors, including temperature, fluid salinity and fluid immiscibility, and is further complicated by the fact that quartz exhibits both prograde and retrograde solubility behavior, depending on the fluid temperature and salinity. Using the PVTX properties of H2O-NaCl, the petrographic and microthermometric properties of fluid inclusions trapped at various locations within the hydrothermal system have been predicted. Vapor-rich inclusions are trapped as a result of the retrograde temperature-dependence of quartz solubility as the convecting fluid is heated in the vicinity of the magmatic heat source. Coexisting liquid-rich and vapor-rich inclusions are also trapped in this region when quartz precipitates as a result of fluid immiscibility that lowers the overall bulk quartz solubility in the system. Fluid inclusions trapped in the shallow subsurface near the seafloor vents and in the underlying stockwork are liquid-rich with homogenization temperatures of 200–400°C and salinities close to that of seawater. Volcanogenic massive sulfide (VMS) deposits represent the uplifted and partially eroded remnants of fossil submarine hydrothermal systems, and the relationship between fluid-inclusion properties and location within the hydrothermal system described here can be used in exploration for VMS deposits to infer the direction towards potential massive sulfide ore.

Paleoredox conditions, hydrothermal history, and target vectoring in the Macmillan Pass base-metal district, Yukon, Canada: 2 – Pyrite paragenesis and mineral chemistry

2021 ◽  
Vol 59 (5) ◽  
pp. 1233-1259
Author(s):  
Claire Leighton ◽  
Daniel Layton-Matthews ◽  
Jan M. Peter ◽  
Michael G. Gadd ◽  
Alexandre Voinot ◽  
...  
Keyword(s):  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Mineral Chemistry ◽  
Hydrothermal Activity ◽  
Unconsolidated Sediments ◽  
Lateral Migration ◽  
Sulfide Mineralization ◽  
Ambient Seawater ◽  
Clastic Sediment ◽  
Icp Ms

ABSTRACT The MacMillan Pass district in Yukon, Canada, hosts the Tom and Jason clastic sediment-hosted Zn-Pb-Ag-(Ba) deposits. Pyrite-bearing drill core samples were collected from seven drill holes that intersected sulfide mineralization and time-stratigraphically equivalent rocks at varied spatial distances extending up to 3 km away from the deposits to assess the relative timing of pyrite mineralization and the chemistry of pyrite paragenesis. There are four pyrite morphologies: framboids and polyframboids (Py1), subhedral to euhedral inclusion-free crystals (Py2a), silicate inclusion-bearing nodules with serrated edges (Py2b), and euhedral idiomorphic overgrowths on preexisting pyrite morphologies (Py3). These morphological varieties correspond in time from syngenetic to earliest diagenetic growth (Py1), early to late diagenetic growth (Py2a, Py2b), and metamorphic crystallization and/or recrystallization of previous textural varieties (Py3). A representative subset of pyrite grains was analyzed for trace element contents and distributions by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). Analyses by LA-ICP-MS reveal that each textural variety of pyrite has a distinct trace element composition that also varies depending on stratigraphic unit. A suite of clastic sediment-hosted sulfide mineralization-related elements was incorporated into Py2 within sulfide mineralized units at greater abundances than that in unmineralized units (e.g., Zn, As, Pb, Tl, Bi). Lead abundances and Pb/Se and As/Mo values in pyrite are the most robust vectoring tools documented. The timing for clastic sediment-hosted Zn-Pb mineralization was syn and/or post late diagenesis (Py2b). A Ba-enriched horizon was identified in rocks and this is interpreted to be the distal time-stratigraphic equivalent unit to Zn-Pb mineralization. The Ba-enriched horizon contains Py2 with anomalous metal (Tl, Co, Mn, Cd, Zn, Sb) contents and abundant macroscopic baryte, and it is interpreted to represent the distal expression of sulfide mineralization-forming hydrothermal activity. Four genetic models for mineralization are reviewed; however, the only model that is consistent with our whole rock and pyrite geochemistry involves venting of buoyant hydrothermal fluid, mixing with ambient seawater, and remaining or sinking into unconsolidated sediments, with lateral migration up to 2–3 km from the vent source.

scholarly journals Trace element analyses of fluid inclusions using laser ablation ICP-MS

2018 ◽  
Vol 3 (1) ◽  
pp. 8-15 ◽  
Author(s):  
Cong-ying Li ◽  
Yu-hang Jiang ◽  
Yan Zhao ◽  
Chan-chan Zhang ◽  
Ming-xing Ling ◽  
...  
Keyword(s):  
Laser Ablation ◽  
Trace Element ◽  
Fluid Inclusions ◽  
Icp Ms

Comparison of fluid processes in coexisting wolframite and quartz from a giant vein-type tungsten deposit, South China: Insights from detailed petrography and LA-ICP-MS analysis of fluid inclusions

2019 ◽  
Vol 104 (8) ◽  
pp. 1092-1116 ◽  
Author(s):  
Jun-Yi Pan ◽  
Pei Ni ◽  
Ru-Cheng Wang
Keyword(s):  
Fluid Inclusion ◽  
Fluid Inclusions ◽  
South China ◽  
Inductively Coupled Plasma ◽  
Fluid Phase ◽  
Fluid Temperature ◽  
Depositional Sequence ◽  
Ms Analysis ◽  
Icp Ms ◽  
Tungsten Mineralization

Abstract Granite-related wolframite-quartz veins are the world's most important tungsten mineralization and production resource. Recent progress in revealing their hydrothermal processes has been greatly facilitated by the use of infrared microscopy and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analysis of both quartz- and wolframite-hosted fluid inclusions. However, owing to the paucity of detailed petrography, previous fluid inclusion studies on coexisting wolframite and quartz are associated with a certain degree of ambiguity. To better understand the fluid processes forming these two minerals, free-grown crystals of intergrown wolframite and quartz from the giant Yaogangxian W deposit in South China were studied using integrated in situ analytical methods including cathodoluminescence (CL) imaging, infrared microthermometry, Raman microspectroscopy, and fluid inclusion LA-ICP-MS analysis. Detailed crystal-scale petrography with critical help from CL imaging shows repetition of quartz, wolframite, and muscovite in the depositional sequence, which comprises a paragenesis far more complex than previous comparable studies. The reconstruction of fluid history in coexisting wolframite and quartz recognizes at least four successive fluid inclusion generations, two of which were entrapped concurrently with wolframite deposition. Fluctuations of fluid temperature and salinity during precipitation of coexisting wolframite and quartz are reflected by our microthermometry results, according to which wolframite-hosted fluid inclusions do not display higher homogenization temperature or salinity than those in quartz. However, LA-ICP-MS analysis shows that both primary fluid inclusions in wolframite and quartz-hosted fluid inclusions associated intimately with wolframite deposition are characterized by strong enrichment in Sr and depletion in B and As compared to quartz-hosted fluid inclusions that are not associated with wolframite deposition. The chemical similarity between the two fluid inclusion generations associated with wolframite deposition implies episodic tungsten mineralization derived from fluids exhibiting distinct chemical signatures. Multiple chemical criteria including incompatible elements and Br/Cl ratios of fluid inclusions in both minerals suggest a magmatic-sourced fluid with the possible addition of sedimentary and meteoric water. Combined with microthermometry and Raman results, fluid chemical evolution in terms of B, As, S, Sr, W, Mn, Fe, and carbonic volatiles collectively imply fluid phase separation and mixing with sedimentary fluid may have played important roles in wolframite deposition, whereas fluid cooling and addition of Fe and Mn do not appear to be the major driving factor. This study also shows that fluid inclusions in both wolframite and coexisting quartz may contain a substantial amount of carbonic volatiles (CO2 ± CH4) and H3BO3. Ignoring the occurrence of these components can result in significant overestimation of apparent salinity and miscalculation of LA-ICP-MS elemental concentrations. We suggest that these effects should be considered critically to avoid misinterpretation of fluid inclusion data, especially for granite-related tungsten-tin deposits.

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