Geochemistry of pink corundum-bearing feldspathic gneiss, Frenchvale quarry, Cape Breton Island, Canada: metamorphism of albitised, Fe-poor clastic rocks

2019 ◽  
Vol 83 (02) ◽  
pp. 249-260
Author(s):  
J. Victor Owen ◽  
Jacob J. Hanley ◽  
Mitchell J. Kerr ◽  
Matthew Stimson ◽  
Brandon Boucher

AbstractFrenchvale quarry, once mined for dolomitic marble, contains pink corundum-bearing, quartz-free/-poor, feldspathic gneiss that is unusually sodic (~7% wt.% Na2O) and iron-poor (~0.6 wt.% Fe2O3), but has silica, alumina and immobile trace-element contents resembling those of suspended fluvial particulate matter (e.g. in the Congo River). The protolith of the gneiss, interpreted as a fine-grained clastic sediment deposited offshore, evidently was albitised prior to deformation and regional metamorphism. Variably-altered gneiss samples show a narrow range of δ18OVSMOW values (8.1 to 10.7‰) and no systematic differences in bulk O isotope composition as a function of alteration intensity. With the exception of an extensively fuchsitised zone adjacent to a thick (1.2 m), cross-cutting quartz vein that contains H2O–NaCl+CO2+CH4-bearing fluid inclusions, the O isotope data do not support interaction of the gneiss with an externally-derived fluid phase except at low fluid:rock ratio, even where granodiorite occurs in direct contact with the gneiss. Fluid inclusions in the quartz vein have bulk $X_{{\rm H}_2{\rm O}}$, $X_{{\rm C}{\rm O}_{\rm 2}}$ and $X_{{\rm C}{\rm H}_{\rm 4}}$ values (in mol.%) of 99.60, 0.14 and 0.26, respectively, as determined by gas chromatography. Although the protolith of the gneiss was associated with carbonate platformal rocks (now marble), corundum is confined to the feldspathic rocks. These feldspathic rocks lack calc-silicate minerals; they are not skarns. As such, they are distinct from well-known Himalayan sapphire and ruby deposits cited previously as analogues of the Frenchvale corundum occurrence.

1992 ◽  
Vol 29 (8) ◽  
pp. 1701-1716 ◽  
Author(s):  
Julie K. Vry ◽  
Philip E. Brown

The results of field mapping and carbon isotope and phase equilibria studies suggest that two different, locally controlled fluid regimes existed during at least the early phases of high-grade metamorphism in the north Cauchon Lake region, Pikwitonei granulite domain, Manitoba, Canada. During the prograde stages of high-grade "anticlockwise" regional metamorphism, rocks already metamorphosed to at least sillimanite grade were thermally metamorphosed at temperatures near 900 °C by the intrusion of a charnockitic magma. It is likely that this magma released an oxidizing, CO2-bearing, probably CO2-rich fluid phase while the region was still at relatively shallow depths. Fluid migration was channelized along the intrusive contact, and local fluid buffering characterized many of the country rocks. The light carbon isotope values of graphites (gr) and CO2 in cordierites (crd) in pelitic lithologies (δ13Cgr = −41.8 to −30.4; δ13Ccrd = −31.8 to −34.9), and the low oxygen fugacities in many samples rule out infiltration of these units by large amounts of an externally derived CO2-rich fluid phase. Texturally early CO2-rich fluid inclusions occur in the cores of garnets in a variety of rock types along the intrusive contact. These fluid inclusions were probably trapped during early garnet growth at high temperatures and relatively low pressures, and appear to have undergone limited or no subsequent reequilibration. They do not appear to provide direct information about the highest regional metamorphic temperature and pressure conditions to have affected the region (750 °C and 7 kbar (1 kbar = 100 MPa)) but may instead retain evidence of the prograde metamorphic path. These studies demonstrate the importance of local controls on the sources, compositions, timing, and transport of metamorphic fluids in the north Cauchon Lake region.


2011 ◽  
Vol 48 (10) ◽  
pp. 1369-1385 ◽  
Author(s):  
Eva S. Schandl ◽  
Michael P. Gorton ◽  
Colin J. Bray

The Lac Panache (Nipissing) gabbro intrudes Huronian metasediments ca. 40 km southwest of the Sudbury Igneous Complex. The gabbro contains disseminated sulfides and is in contact with a chalcopyrite-rich quartz vein that crystallized from highly saline fluids (46.8 ± 3 equivalent wt.% NaCl) at a minimum temperature of 420 ± 27 °C. Chloride and carbonate inclusions in opened fluid inclusion cavities in the vein suggest that the brine contained dissolved metals (in addition to NaCl), such as Fe, Cu, Mn, and Co. The weakly altered quartz vein postdated regional metamorphism and was probably contemporaneous with the 1.7 Ga felsic magmatism and attendant albite alteration in the area. Cl-rich scapolite in the gabbro and highly saline fluid inclusions in the quartz vein suggest the existence of circulating hot brine throughout the tectonic evolution of the region. The 2.2 Ga old gabbro contains an abundance of Cl-rich scapolite intergrown with pyrrhotite and chalcopyrite that formed during the early hydrothermal (deuteric) alteration of the gabbro.


Minerals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 94
Author(s):  
Xiaoxue Tong ◽  
Kaarel Mänd ◽  
Yuhao Li ◽  
Lianchang Zhang ◽  
Zidong Peng ◽  
...  

Banded iron formations (BIFs) are enigmatic chemical sedimentary rocks that chronicle the geochemical and microbial cycling of iron and carbon in the Precambrian. However, the formation pathways of Fe carbonate, namely siderite, remain disputed. Here, we provide photomicrographs, Fe, C and O isotope of siderite, and organic C isotope of the whole rock from the ~2.52 Ga Dagushan BIF in the Anshan area, China, to discuss the origin of siderite. There are small magnetite grains that occur as inclusions within siderite, suggesting a diagenetic origin of the siderite. Moreover, the siderites have a wide range of iron isotope compositions (δ56FeSd) from −0.180‰ to +0.463‰, and a relatively negative C isotope composition (δ13CSd = −6.20‰ to −1.57‰). These results are compatible with the reduction of an Fe(III)-oxyhydroxide precursor to dissolved Fe(II) through microbial dissimilatory iron reduction (DIR) during early diagenesis. Partial reduction of the precursor and possible mixing with seawater Fe(II) could explain the presence of siderite with negative δ56Fe, while sustained reaction of residual Fe(III)-oxyhydroxide could have produced siderite with positive δ56Fe values. Bicarbonate derived from both DIR and seawater may have provided a C source for siderite formation. Our results suggest that microbial respiration played an important role in the formation of siderite in the late Archean Dagushan BIF.


1976 ◽  
Vol 13 (3) ◽  
pp. 405-421 ◽  
Author(s):  
Lee C. Pigage

Pelitic metasediments immediately southwest of Yale, British Columbia contain mineral assemblages characteristic of staurolite through sillimanite zones of the Barrovian facies series. Microprobe analyses of major constituent phases in the pelites are combined with linear regression techniques to formulate probable kyanite- and sillimanite-forming reactions.A zone some 3 km wide contains the assemblage staurolite–kyanite–garnet–biotite–muscovite–quartz–plagioclase-ilmenite-rutile, which is univariant in AFM projection. Within precision limits of microprobe analysis, this assemblage is also univariant using linear regression techniques. Univariant relations are possible if [Formula: see text] with the composition of the fluid phase being buffered by the progressing reaction. This assemblage emphasizes the need for precise analyses when using the regression method, since minor components are often within permissible error limits rather than being balanced.Pelitic and calc-silicate assemblages from the metasediments restrict estimates of pressure–temperature conditions during regional metamorphism to 6–8 kbar and 550–770 °C. Pseudomorphs after andalusite indicate that contact metamorphism preceded regional upgrading of the pelites.


Author(s):  
Tao Luo ◽  
Qiuli Li ◽  
Xiaoxiao Ling ◽  
Yang Li ◽  
Chuan Yang ◽  
...  

Zircon U-Pb geochronology and Hf-O isotope composition can provide important information on geological events. The matrix-matched reference material is routinely used to yield accurate and precise zircon U-Pb ages and...


2019 ◽  
Vol 104 (8) ◽  
pp. 1092-1116 ◽  
Author(s):  
Jun-Yi Pan ◽  
Pei Ni ◽  
Ru-Cheng Wang

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.


Minerals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 828
Author(s):  
Jungrae Noh ◽  
Changyeob Kim ◽  
Vinod O. Samuel ◽  
Yirang Jang ◽  
Seung-Ik Park ◽  
...  

In this contribution, we report the metasomatic characteristics of a lamprophyre dyke–marble contact zone from the Hongseong–Imjingang belt along the western Gyeonggi Massif, South Korea. The lamprophyre dyke intruded into the dolomitic marble, forming a serpentinized contact zone. The zone consists of olivine, serpentine, calcite, dolomite, biotite, spinel, and hematite. Minor F and Cl contents in the serpentine and biotite indicate the composition of the infiltrating H2O-CO2 fluid. SiO2 (12.42 wt %), FeO (1.83 wt %), K2O (0.03 wt %), Sr (89 ppm), U (0.7 ppm), Th (1.44 ppm), and rare earth elements (REEs) are highly mobile, while Zr, Cr, and Ba are moderately mobile in the fluid. Phase equilibria modelling suggests that the olivine, spinel, biotite, and calcite assemblage might be formed by the dissolution of dolomite at ~700 °C, 130 MPa. Such modelling requires stable diopside in the observed conditions in the presence of silica-saturated fluid. The lack of diopside in the metasomatized region is due to the high K activity of the fluid. Our log activity K2O (aK2O)–temperature pseudosection shows that at aK2O~−40, the olivine, spinel, biotite, and calcite assemblage is stable without diopside. Subsequently, at ~450 °C, 130 MPa, serpentine is formed due to the infiltration of H2O during the cooling of the lamprophyre dyke. This suggests that hot H2O-CO2 fluids with dissolved major and trace elements infiltrated through fractures, grain boundaries, and micron-scale porosity, which dissolved dolomite in the marble and precipitated the observed olivine-bearing peak metasomatic assemblage. During cooling, exsolved CO2 could increase the water activity to stabilize the serpentine. Our example implies that dissolution-reprecipitation is an important process, locally and regionally, that could impart important textural and geochemical variations in metasomatized rocks.


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