scholarly journals Mineralogy, Fluid Inclusions, and Oxygen Isotope Geochemistry Signature of Wolframite to Scheelite and Fe,Mn Chlorite Veins from the W, (Cu,Mo) Ore Deposit of Borralha, Portugal

Minerals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 24
Author(s):  
Iuliu Bobos ◽  
Carlos Marques de Sá ◽  
Fernando Noronha

Scheelitization of Mn-bearing wolframite, scheelite, quartz, and Fe,Mn-chlorite veins was identified in the W, (Cu,Mo) ore deposits of Borralha, by optical microscopy, electron-microprobe analysis, and stable isotope geochemistry. Fluid inclusions derived scheelite crystallization temperature was compared with the oxygen isotope temperature estimated. Scheelite was formed mainly during stage I from a low salinity aqueous-carbonic fluid dominated by CO2, where the homogenization temperature (Th) decreased from 380 °C to 200 °C (average of 284 °C). As temperature decreased further, the aqueous-carbonic fluid became dominated by CH4 (Stage II; (average Th = 262 °C)). The final stage III corresponds to lower temperature mineralizing aqueous fluid (average Th = 218 °C). In addition, salinity gradually decreased from 4.8 wt.% to 1.12 wt.%. The δ18OFluid values calculated for quartz-water and wolframite-water fractionation fall within the calculated magmatic water range. The ∆quartz-scheelite fractionation occurred at about 350–400 °C. The ∆chlorite-water fractionation factor calculated is about +0.05‰ for 330 °C, dropping to −0.68‰ and −1.26‰ at 380 °C and 450 °C, respectively. Estimated crystallizing temperatures based on semi-empirical chlorite geothermometers range from 373 °C to 458 °C and 435 °C to 519 °C. A narrower temperature range of 375 °C to 410 °C was estimated for Fe,Mn-chlorite crystallization.

1987 ◽  
Vol 51 (362) ◽  
pp. 477-481 ◽  
Author(s):  
R. C. Burruss

AbstractDiagenetic palaeotemperatures determined from aqueous fluid inclusions can be affected by re-equilibration during burial heating. Calculations based on the observed behaviour of inclusions in fluorite under external confining pressure allows prediction of the temperatures and depths of burial necessary to initiate re-equilibration of aqueous inclusions in the common size range 40 to 4 µm. Heating of 20° to 60°C over the initial trapping temperature may cause errors of 10° to 20°C in the homogenization temperature. This suggests re-equilibration may cause aqueous inclusions in carbonates to yield a poor record of their low-temperature history, but a useful record of the maximum temperature experienced by the host rock. Previous work suggests inclusions containing petroleum fluids will be less susceptible to re-equilibration.


2012 ◽  
Vol 4 (2) ◽  
Author(s):  
Ronald Bakker

AbstractThe bulk salinity cannot be directly obtained from the dissolution temperatures of halite in highly saline fluid inclusions that contain solid, liquid, and vapour at room temperature. At least two of the following independent parameters must be determined to estimate the bulk composition and density of these inclusions: 1. dissolution temperature of halite in the presence of vapour; 2. total homogenization temperature of liquid and vapour; and 3. volume fraction of the vapour phase. A new V m-x diagram for phase stabilities in the H2O-NaCl system has been constructed to obtain these bulk fluid properties from inclusions that homogenize liquid and vapour phase at higher temperatures than dissolution of halite.


2019 ◽  
Vol 114 (6) ◽  
pp. 1033-1056 ◽  
Author(s):  
Andreas Audétat

Abstract A fundamental question in the study of magmatic-hydrothermal ore deposits is whether the mineralization potential of intrusions was already predetermined by the metal content of the exsolving fluids. The present study aims at addressing this question by reviewing the large number of microanalytical data (mostly laser-ablation ICP-MS data) obtained on fluid inclusions from this type of ore deposits over the last 20 years. Published data sets were screened for analyses of high-temperature fluid inclusions that are representative of premineralization fluids. A set of criteria was developed to distinguish such fluids from later, lower temperature fluids. In order to compensate differences in absolute metal concentrations caused by fluid immiscibility, all element concentrations were normalized to Na. A numerical model was developed to explore at which stage different metals are most efficiently extracted from a cooling pluton. The results suggest that the timing of most efficient metal extraction varies from metal to metal and strongly depends on pressure, the fluid/melt partition coefficient and the bulk mineral-melt partition coefficient. As a consequence, fluid compositions were chosen over the entire range of Cs/Na ratios recorded from a given pluton, as this ratio gives an indication of the fractionation degree of the silicate melts from which a fluid exsolved. In order to avoid bias toward occurrences from which a large amount of data are available, maximum four intermediate-density (ID)-type fluid inclusion assemblages plus four brines assemblages were chosen from each occurrence. Using the above-mentioned criteria, 169 fluid compositions from 12 Cu (Mo, Au) mineralized intrusions, 10 Sn/W mineralized intrusions, two Mo mineralized intrusions, and one U-Th-REE mineralized intrusion were finally chosen and plotted in graphs of X/Na versus Cs/Na. The results reveal that Sn- and Cu-mineralizing fluids contained more Sn and Cu, respectively, than the fluids analyzed from barren and Mo or U-Th REE mineralized intrusions. Positive correlations between fluid metal content and mineralization potential may exist also for W and REEs, whereas for Mo no such trend is evident. Therefore, at least for certain metals, the metal content of high-temperature fluid inclusions can be used as an indicator of the type and extent of mineralization. However, elevated metal concentrations are present also in some fluids from barren intrusions, which implies that the mineralization potential additionally depends on other factors such as the size of the intrusion and the development of structures that promote focused fluid flow.


2015 ◽  
Vol 3 (1) ◽  
Author(s):  
Irzal Nur ◽  
Arifudin Idrus ◽  
Subagyo Pramumijoyo ◽  
Agung Harijoko ◽  
Akira Imai

The Baturappe prospect located at southern part of Sulawesi island, Indonesia, is a hydrothermal mineralization district which is characterized by occurrence of epithermal silver-base metal deposits. The mineralization is hosted in basaltic-andesitic volcanic rocks of the late Middle-Miocene Baturappe Volcanics. More than 20 units of quartz – base metal veins are distributed in the area, and one of the most significant is the Bincanai vein. This study is aimed to characterize the mineral paragenesis and to elucidate the physicochemical conditions of the formation of the deposit on the basis of mineral assemblage and fluid inclusion mictrothermometry. Sulphide assemblages in the vein indicate an intermediate sulfidation state epithermal; beside galena and sphalerite as the early stage minerals, chalcopyrite, tennantite, and tetrahedrite are also identified as the later stage. Microthermometric study of fluid inclusions in quartz indicates formation temperature of the vein ranges from about 230 to 280°C Histogram of homogenization temperature suggests that there are two generations of hydrothermal fluid responsible for the ore mineralization in the vein; the higher temperature range represents formation temperature of the base metal (galena, sphalerite), while the lower temperature range is correlate with the precipitation of the rest relatively lower temperature sulphides (chalcopyrite, pyrite, tetrahedrite, tennantite, polybasite, and Bi-Ag-Cu-Fe-bearing sulfide). The sequence is also consistent with the mineral paragenetic. The mean of salinity (2.0–2.5 wt.% NaCl eq.) indicates that fluid responsible for the mineralization in the Bincanai vein is relatively low-salinity fluid.


2020 ◽  
pp. 014459872097451
Author(s):  
Wenqi Jiang ◽  
Yunlong Zhang ◽  
Li Jiang

A fluid inclusion petrographic and microthermometric study was performed on the sandstones gathered from the Yanchang Formation, Jiyuan area of the Ordos Basin. Four types of fluid inclusions in quartz can be recognized based on the location they entrapped. The petrographic characteristics indicate that fluid inclusions in quartz overgrowth and quartz fissuring-I were trapped earlier than that in quartz fissuring-IIa and fissuring-IIb. The homogenization temperature values of the earlier fluid inclusions aggregate around 80 to 90°C; exclusively, it is slightly higher in Chang 6 member, which approaches 95°C. The later fluid inclusions demonstrate high homogenization temperatures, which range from 100 to 115°C, and the temperatures are slightly higher in Chang 9 member. The calculated salinities show differences between each member, including their regression characteristics with burial depth. Combining with the vitrinite reflection data, the sequence and parameters of fluid inclusions indicate that the thermal history of the Yanchang formation mostly relied on burial. Salinity changes were associated with fluid-rock interaction or fluid interruption. Hydrocarbon contained fluid inclusions imply that hydrocarbon generation and migration occurred in the Early Cretaceous. The occurrence of late fluid inclusions implied that quartz cement is a reservoir porosity-loose factor.


1984 ◽  
Vol 79 (5) ◽  
pp. 933-946 ◽  
Author(s):  
Bruce E. Nesbitt ◽  
Fred J. Longstaffe ◽  
David R. Shaw ◽  
Karlis Muehlenbachs

2014 ◽  
Vol 6 (2) ◽  
Author(s):  
Oktay Canbaz ◽  
Ahmet Gökce

AbstractThe Çöpler gold deposit occurs within the stockwork of quartz hosted by the Çöpler granitoid (Eosen) and by surrounding metasediments of Keban metamorphic (Late Paleozoic - Early Mesozoic) and the Munzur limestones (Late Carboniferous - Early Cretaceous).Native gold accompanied by small amounts of chalcopyrite, pyrite, magnetite, maghemite, hematite, fahlerz, marcasite, bornite, galena, sphalerite, specular hematite, goethite, lepidochrosite and bravoitic pyrite within the stockwork ore veinlets. In addition, epidote (pistazite - zoisite), garnet, scapolite, chlorite, tremolite/actinolite, muscovite and opaque minerals were determined within the veinlets occurred in skarn zones.The study of fluid inclusions in quartz veinlets showed that the hydrothermal fluids contain CaCl2, MgCl2 and NaCl and the salinities of the two phases (L+V) inclusions range from 1.7 to 20.6% NaCl equivalent. Salinity values up to 44% were determined within the halite bearing three phases inclusions. Their homogenization temperature values have a wide range from 145.0 to 380.0°C, indicative of catathermal/hypothermal to epithermal conditions. The δ 18O and δD values of the fluid inclusion waters from the Çöpler granitoid correspond to those assigned to Primary Magmatic Water, those from the metasediments of Keban metamorphics fall outside of the Primary Magmatic and are within the Metamorphic Water field. A sample from a quartz vein within the skarn zone hosted by the Munzur limestones has a particularly low δD value.The results suggest that fluids derived from the granitoids were mixed with those derived from the metasediments of Keban metamorphics and the the Munzur limestones and resulting in quartz veinlets in these lithologies and the formation of stockwork ores. In view of the occurrence, the features described and processes envisaged for this study area may be applicable in similar settings.


Geofluids ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-25
Author(s):  
Lu Zhang ◽  
Shao-Yong Jiang ◽  
Suo-Fei Xiong ◽  
Deng-Fei Duan

The Fuzishan Cu-Mo deposit is located in the Edong district of the Middle-Lower Yangtze River Metallogenic Belt, China. The orebodies mainly occurred as lenticular and bedded shapes in the skarn zone between the Lower Permian Qixia Formation carbonate rocks and the quartz diorite. Four paragenetic stages have been recognized based on petrographic observations: (1) prograde skarn stage, (2) retrograde skarn stage, (3) quartz-sulfide stage, and (4) carbonate stage. Six fluid inclusion types were recognized: S1(vapor + liquid + halite ± other daughter minerals), S2(vapor + liquid + daughter minerals except halite), LV(rich liquid + vapor), VL(rich vapor + liquid), V (vapor), and L (liquid) types. Fluid inclusion studies show distinct variations in composition, final homogenization temperature, and salinity in four stages. Daughter minerals of the primary fluid inclusions include chalcopyrite, molybdenite, hematite, anhydrite, calcite, and halite in the prograde skarn stage and hematite, calcite, and sulfide (?) in the retrograde skarn stage. No daughter minerals occurred in the quartz-sulfide and carbonate stages. Final homogenization temperatures recorded in these stages are from 405 to >550°C, from 212 to 498°C, from 150 to 485°C, and from 89 to 223°C, respectively, while salinities are from 3.7 to 42.5, from 2.6 to 18.5, from 2.2 to 17.9, and from 0.2 to 11.5 wt.% NaCl equivalent, respectively. The coexisting VLand S1type fluid inclusions show similar homogenization temperature of 550 to about 650°C in the prograde skarn stage, indicating that immiscibility occurred at lithostatic pressure of 700 bars to perhaps 1000 bars, corresponding to a depth of 2.6 km to about 3.7 km. The coeval VLand LVtypes fluid inclusions with homogenization temperature of 350 to 400°C in the late retrograde skarn and quartz-sulfide stages suggest that boiling occurred under hydrostatic pressure of 150 to 280 bars, equivalent to a depth of 1.5 to 2.8 km. Mo mineralization in the retrograde stage predated Cu mineralization which mainly occurred in the quartz-sulfide stage. Fluid compositions indicate that ore-forming fluid has highfO2and rich Cu and Mo concentration in the early stage, while relatively lowerfO2and poor Cu and Mo concentration in the middle to late stages. Microthermometric data show a decreasing trend in temperature and salinity in the fluid evolution process. Decreasing temperature and boiling event may be the main factors that control the ore precipitation.


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