scholarly journals Characteristics of the Ahmadabad hematite/barite deposit, Iran – studies of mineralogy, geochemistry and fluid inclusions

Geologos ◽  
2018 ◽  
Vol 24 (1) ◽  
pp. 55-68 ◽  
Author(s):  
Amir Haji Babaei ◽  
Alireza Ganji

Abstract The Ahmadabad hematite/barite deposit is located to the northeast of the city of Semnan, Iran. Geostructurally, this deposit lies between the Alborz and the Central Iran zones in the Semnan Subzone. Hematite-barite mineralisation occurs in the form of a vein along a local fault within Eocene volcanic host rocks. The Ahmadabad deposit has a simple mineralogy, of which hematite and barite are the main constituents, followed by pyrite and Fe-oxyhydroxides such as limonite and goethite. Based on textural relationships between the above-mentioned principal minerals, it could be deduced that there are three hydrothermal mineralisation stages in which pyrite, hematite and barite with primary open space filling textures formed under different hydrothermal conditions. Subsequently, in the supergene stage, goethite and limonite minerals with secondary replacement textures formed under oxidation surficial conditions. Microthermometric studies on barite samples show that homogenisation temperatures (TH) for primary fluid inclusions range from 142 to 256°C with a temperature peak between 200 and 220°C. Salinities vary from 3.62 to 16.70 NaCl wt% with two different peaks, including one of 6 to 8 NaCl wt% and another of 12 to 14 NaCl wt%. This indicates that two different hydrothermal waters, including basinal and sea waters, could have been involved in barite mineralisation. The geochemistry of the major and trace elements in the samples studied indicate a hydrothermal origin for hematite and barite mineralisation. Moreover, the Fe/Mn ratio (>10) and plots of hematite samples of Ahmadabad ores on Al-Fe-Mn, Fe-Mn-(Ni+Co+ Cu)×10, Fe-Mn-SiX2 and MnO/TiO2 – Fe2O3/TiO2 diagrams indicate that hematite mineralisation in the Ahmadabad deposit occurred under hydrothermal conditions. Furthermore, Ba and Sr enrichment, along with Pb, Zn, Hg, Cu and Sb depletion, in the barite samples of Ahmadabad ores are indicative of a low temperature hydrothermal origin for the deposit. A comparison of the ratios of LaN/YbN, CeN/YbN, TbN/LaN, SmN/NdN and parameters of Ce/Ce* and La/La* anomalies of the hematite, barite, host volcanic rocks and quartz latite samples to each other elucidate two important points: 1) the barite could have originated from volcanic host rocks, 2) the hematite could have originated from a quartz latite lithological unit. The chondrite normalised REE patterns of samples of hematite barite, volcanic host rocks and quartz latite imply that two different hydrothermal fluids could be proposed for hematite and barite mineralisation. The comparison between chondrite normalised REE patterns of Ahmadabad barite with oceanic origin barite and low temperature hydrothermal barite shows close similarities to the low temperature hydrothermal barite deposits.

2019 ◽  
Vol 55 (1) ◽  
pp. 202
Author(s):  
Foteini Aravani ◽  
Lambrini Papadopoulou ◽  
Vasileios Melfos ◽  
Triantafillos Soldatos ◽  
Triantafillia Zorba ◽  
...  

The volcanic rocks of Kornofolia area, Evros, host a number of epithermal-type veins. The host rocks are Oligocene calc-alkaline andesites to rhyo-dacites. The andesites form hydrothermal breccias and show hydrothermal alteration. The veins comprise mainly silica polymorphs such as quartz, chalcedony and three types of opal (milky white, transparent and green). Amethyst also forms in veins at the same area. Apart from the silica polymorphs, the veins are accompanied by calcite and zeolites. The main aim of this study is the characterization of the silica polymorphs. Using FT-IR analyses, variations in the crystal structure of the three opals were recognized. The green opal is found to be more amorphous than the other two types. Fluid-inclusion measurements were performed in calcite and were compared with amethyst from previous studies. The Th is between 121-175 °C and the Te between -22.9 and -22.4 °C. The salinities range from 0.9 to 4.5 wt % NaCl equiv.


2021 ◽  
Vol 25 (2) ◽  
pp. 139-156
Author(s):  
Fernando Helí Romero Ordóñez ◽  
Andrés Felipe González-Durán ◽  
Javier García-Toloza ◽  
Jimmy Rotlewicz Cohen ◽  
Carlos Julio Cedeño Ochoa ◽  
...  

The Cunas mine is currently one of the major producers of fine emeralds in Colombia; its emeralds typically display a magnificent green hue, which is highly appreciated in the world market. The mineralization is found in vanadium-rich black shales of the Muzo formation; emeralds occur in pockets within hydrothermal veins and breccias, consisting mostly of calcite, dolomite, albite, quartz, and minor pyrite, parisite-(Ce), and fluorite; hydrothermal alteration is pervasive and dominated by albitization and carbonatization. Emerald-hosted fluid inclusions are highly abundant and remarkably large and complex. Poly-phase inclusions are ubiquitous, occur both in emeralds and gangue minerals, and consist of two daughter crystals (typically halite and calcite or siderite; exceptionally parisite-(Ce)), a liquid brine, a CO2-N2-CH4-rich gas bubble, and occasionally minor liquid CO2. Vapor-rich inclusions were observed in quartz, and two-phase inclusions were identified in calcite and dolomite, thus suggesting a complex fluid evolution. Microthermometry analysis indicates the emerald-forming fluids were trapped at relatively low temperature ≈ 260-340°C and pressure ≈ 875-2400 kbar, with relatively high density —1.03 g/cm³—, and elevated salinity 39% NaCl eq. Wt.; other aqueous components detected include CaCl2, KCl, and FeCl2. Based on these data, we propose the emerald mineralization at the Cunas mine was originated by the mixing of two hydrothermal fluids of different sources; one fluid with high salinity derived from evaporite dissolution, responsible for the albitization of the host rocks; the second is a calcium-rich fluid evolved from connate waters, which was equilibrated by the interaction with calcareous and organic-rich wall rocks. As a result, emerald mineralization took place at structurally favorable sites where fluid mixing was promoted. The described geological and physicochemical features for the Cunas mine, are in agreement with an epigenetic sediment-hosted mineralization —Colombian-type— formed by the circulation and mixing of relatively low-temperature non-magmatic fluids.


2021 ◽  
pp. 1-26
Author(s):  
Taylor A. Ducharme ◽  
Christopher R.M. McFarlane ◽  
Deanne van Rooyen ◽  
David Corrigan

Abstract The Flowers River Igneous Suite of north-central Labrador comprises several discrete peralkaline granite ring intrusions and their coeval volcanic succession. The Flowers River Granite was emplaced into Mesoproterozoic-age anorthosite–mangerite–charnockite–granite (AMCG) -affinity rocks at the southernmost extent of the Nain Plutonic Suite coastal lineament batholith. New U–Pb zircon geochronology is presented to clarify the timing and relationships among the igneous associations exposed in the region. Fayalite-bearing AMCG granitoids in the region record ages of 1290 ± 3 Ma, whereas the Flowers River Granite yields an age of 1281 ± 3 Ma. Volcanism occurred in three discrete events, two of which coincided with emplacement of the AMCG and Flowers River suites, respectively. Shared geochemical affinities suggest that each generation of volcanic rocks was derived from its coeval intrusive suite. The third volcanic event occurred at 1271 ± 3 Ma, and its products bear a broad geochemical resemblance to the second phase of volcanism. The surrounding AMCG-affinity ferrodiorites and fayalite-bearing granitoids display moderately enriched major- and trace-element signatures relative to equivalent lithologies found elsewhere in the Nain Plutonic Suite. Trace-element compositions also support a relationship between the Flowers River Granite and its AMCG-affinity host rocks, most likely via delayed partial melting of residual parental material in the lower crust. Enrichment manifested only in the southernmost part of the Nain Plutonic Suite as a result of its relative proximity to multiple Palaeoproterozoic tectonic boundaries. Repeated exposure to subduction-derived metasomatic fluids created a persistent region of enrichment in the underlying lithospheric mantle that was tapped during later melt generation, producing multiple successive moderately to strongly enriched magmatic episodes.


2015 ◽  
Vol 52 (12) ◽  
pp. 1093-1108 ◽  
Author(s):  
Bruno Lafrance

The Larder Lake – Cadillac deformation zone (LLCDZ) is one of two major, auriferous, deformation zones in the southern Abitibi subprovince of the Archean Superior Province. It hosts the Cheminis and the giant Kerr Addison – Chesterville deposits within a strongly deformed band of Fe-rich tholeiitic basalt and komatiite of the Larder Lake Group (ca. 2705 Ma). The latter is bounded on both sides by younger, less deformed, Timiskaming turbidites (2674–2670 Ma). The earliest deformation features are F1 folds affecting the Timiskaming rocks, which formed either during D1 extensional faulting or during early D2 north–south shortening related to the opening and closure, respectively, of the Timiskaming basin. Continued shortening during D2 imbricated the older volcanic rocks and turbidites and produced regional F2 folds with an axial planar S2 cleavage. D2 deformation was partitioned into the weaker band of volcanic rocks, producing the strong S2 foliation, L2 stretching lineation, and south-side-up shear sense indicators, which characterize the LLCDZ. Gold is present in quartz–carbonate veins in deformed fuchsitic komatiites (carbonate ore) and turbiditic sandstone (sandstone-hosted ore), and in association with disseminated pyrite in altered Fe-rich tholeiitic basalts (flow ore). All host rocks underwent strong mass gains in CO2, S, K2O, Ba, As, and W, during sericitization, carbonatization, and sulphidation of the host rocks, suggesting that they interacted with the same hydrothermal fluids. Textural relationships between alteration minerals and S2 cleavage indicate that mineralization is syn-cleavage. Thus, gold was deposited as hydrothermal fluids migrated upward along the LLCDZ during contractional, D2 south-side-up shearing. The gold zones were subsequently modified during D3 reactivation of the LLCDZ as a dextral transcurrent fault zone.


Geologos ◽  
2014 ◽  
Vol 20 (3) ◽  
pp. 201-214 ◽  
Author(s):  
Alireza Zarasvandi ◽  
Nazanin Zaheri ◽  
Houshang Pourkaseb ◽  
Abbas Chrachi ◽  
Hashem Bagheri

Abstract The Permian carbonate-hosted Farsesh barite deposit is located southeast of the City of Aligudarz in the province of Lorestan, Iran. Structurally, this deposit lies in the Zagros metallogenic belt and the Sanandaj-Sirjan Zone. Barite mineralisations occur as open-space flling veins, and as massive and replacement ores along fractures, faults and shear zones of the Permian carbonate host rocks. In order to determine the structure, in addition to pe-trographic and fuid-inclusions studies, an ICP-MS analysis was carried out in order to measure the major as well as the trace and rare earth elements. The Farsesh barite deposit has a simple mineralogy, of which barite is the main mineral, followed by calcite, dolomite, quartz, and opaque minerals such as Fe-oxides. Replacement of bar-ite by calcite is common and is more frequent than space-flling mineralisation. Sulphide minerals are minor and mainly consist of chalcopyrite and pyrite, which are altered by weathering to covellite, malachite and azurite. Petrographic analysis and micro-thermometry were carried out on the two-phase liquid/vapour inclusions in ellipsoidal or irregularly shaped minerals ranging in size from 5–10 µm. The measurements were conducted on fuid inclusions during the heating and subsequent homogenisation in the liquid phase. The low homogenisation temperatures (200–125°C) and low to moderate salinity (4.2–20 eq wt% NaCl) indicate that the barite had precipitated from hydrothermal basinal water with low to moderate salinity. It appears from the major and trace elements that geochemical features such as Ba and Sr enrichment in the barite samples was accompanied by depletion of Pb, Zn, Hg, Cu and Sb. The geochemistry of the rare earth elements, such as low σREE concentrations, LREE-enrichment chondrite-normalised REE patterns, the negative Ce and positive Eu anomalies, the low Ce/La ratio and the positive La and Gd anomalies, suggest that the Farsesh barite was deposited from hydrothermally infuenced sea water. The Farsesh deposit contains low-temperature hydrothermal barite. The scatter plots of the barite (close to sea water) in different areas on the CeN/SmN versus CeN/YbN diagram support the possibility that the barite was formed from seawater-bearing hydrothermal fuids.


1984 ◽  
Vol 21 (6) ◽  
pp. 731-736 ◽  
Author(s):  
Nathan L. Green ◽  
Paul Henderson

A suite of hy-normative hawaiites, ne-normative mugearite, and calc-alkaline andesitic rocks from the Garibaldi Lake area exhibits fractionated, slightly concave-upward REE patterns (CeN/YbN = 4.5–15), heavy REE contents about 5–10 times the chondritic abundances, and no Eu anomalies. It is unlikely that the REE patterns provide information concerning partial melting conditions beneath southwestern British Columbia because they have probably been modified substantially by upper crustal processes including crustal contamination and (or) crystal fractionation. The REE contents of the Garibaldi Lake lavas are not incompatible with previous interpretations that (1) the hawaiites have undergone considerable fractionation of olivine, plagioclase, and clinopyroxene; and (2) the individual andesitic suites were derived from separate batches of chemically distinct magma that evolved along different high-level crystallization trends. In general, however, the andesites are characterized by lower light REE contents than the basaltic andesites. These differences in LREE abundances may reflect different amounts of LREE-rich accessory phases, such as apatite, sphene, or allanite, assimilated from the underlying quartz diorites.


Geofluids ◽  
2012 ◽  
Vol 12 (4) ◽  
pp. 295-311 ◽  
Author(s):  
M. KOUSEHLAR ◽  
T. B. WEISENBERGER ◽  
F. TUTTI ◽  
H. MIRNEJAD

1988 ◽  
Vol 25 (8) ◽  
pp. 1323-1337 ◽  
Author(s):  
James H. Sevigny

Late Proterozoic amphibolites and ultramafic rocks from the southeastern Canadian Cordillera have been analysed for major and trace elements in order to determine the nature and origin of the protoliths. Geologic relations indicate that these rocks were produced during an episode of continental rifting in the Precambrian. Based on rare-earth-element (REE) patterns, immobile-incompatible-element ratios, and characteristic elemental abundances, amphibolites are subdivided into alkaline and tholeiitic metabasalts. Alkaline basalts are recognized by their steep REE patterns, high Zr/Y, high TiO2 and P2O5 abundances, and low Y/Nb and Ti/Zr. Tholeiitic basalts are subdivided into three groups: (I) high-Mg#, high-field-strength-element (HFSE)-depleted, light-REE (LREE)-enriched tholeiites with flat heavy REE (HREE) patterns; (II) LREE-enriched tholeiites depleted in HREE; and (III) low-Mg# tholeiites with flat REE patterns. Ultramafic rocks occur as boudins of partially recrystallized Cr-spinel-bearing harzburgite or therzolite, enriched in LREE (Ce/Sm = 1.7–1.9), HFSE, CaO, Al2O3, and TiO2 relative to depleted mantle.Geochemical data suggest that the basalts were derived from a heterogeneous mantle source that underwent different degrees of partial melting with variable amounts of subsequent crystal fractionation of the melts. High Mg#, high Cr and Ni abundances, low HFSE abundances, and high olivine saturation temperatures suggest that group I tholeiites are primary mantle melts produced by a relatively high degree of partial melting of a LREE-enriched, HFSE-depleted source. Group II and III basalts have undergone moderate olivine and pryoxene and limited plagioclase fractionation. Mass-balance calculations suggest that the ultramafic rocks represent a crustally contaminated primary-mantle-derived melt.Les éléments majeurs et traces des amphibolites et des ultramafites, d'âge protérozoïque tardif, du sud-est de la Cordillère canadienne ont été analysés dans le but de déterminer la nature et l'origine des protolithes. Les relations géologiques indiquent que ces roches se sont formées durant un épisode de rifting continental dans le Précambrien. Les diagrammes des terres rares, les rapports des éléments immobiles et incompatibles et les compositions chimiques caractéristiques ont permis de subdiviser les amphibolites en métabasaltes tholéiitiques et alcalins. Les basaltes alcalins sont reconnus par les courbes abruptes dans les diagrammes des terres rares, les rapports Zr/Y élevés et les fortes teneurs en TiO2 et P2O5 et les rapports Y/Nb et Ti/Zr faibles. Les basaltes tholéiitiques sont subdivisés en trois groupes : (I) avec Mg# élevé, appauvrissement en éléments de force de champ élevée, tholéiites enrichies en terres rares légères avec courbe horizontale des terres rares lourdes; (II) tholéiites enrichies en terres rares légères et appauvries en terres rares lourdes; et (III) tholéiites avec Mg# faible et avec courbe horizontale des variations des terres rares. Les ultramafites se présentent en boudins formés d'harzburgite incluant un spinelle chromifère partiellement recristallisé ou de therzolite qui sont enrichies en terres rares légères (Ce/Sm = 1,7–1,9), en éléments à force de champ élevée, en CaO, Al2O3 et TiO2, comparativement à un manteau appauvri.


2021 ◽  
Vol 23 (05) ◽  
pp. 787-790
Author(s):  
Abhijit M ◽  
◽  
Suresh Kumar. B. V ◽  

Cowlesite is a Calcium Aluminum silicate CaAl2Si3O106H2O which formed under the hydrothermal conditions of low temperature (1800C) and pressure (1.013250bar). Cowlesite minerals are known for their peculiar occurrence. Synthesis of Cowlesite mineral was carried by suitable stoichiometric composition. Hydrothermal synthesized Cowlesite mineral was characterized by XRD, SEM, and EDAX. It crystallized in the orthorhombic system and a lattice parameter a=23.22Å, b=30.58Å, c=25.01Å, Volume of Unit cell=17758.79Å3, α=β=γ=900. EDAX results show the elemental concentration of raw material which was used.


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