scholarly journals Petrogenesis of the Eudialyte Complex of the Lovozero Alkaline Massif (Kola Peninsula, Russia)

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 581 ◽  
Author(s):  
Julia A. Mikhailova ◽  
Gregory Yu. Ivanyuk ◽  
Andrey O. Kalashnikov ◽  
Yakov A. Pakhomovsky ◽  
Ayya V. Bazai ◽  
...  
Keyword(s):  
Water Solution ◽  
Granite Gneiss ◽  
Gradual Transition ◽  
Eudialyte Group ◽  
Fine Grained ◽  
Phosphorus Mineralization ◽  
Volcaniclastic Rocks ◽  
Layered Complex ◽  
Alkaline Massif ◽  
Fractionation Path

The Lovozero Alkaline Massif intruded through the Archaean granite-gneiss and Devonian volcaniclastic rocks about 360 million years ago, and formed a large (20 × 30 km) laccolith-type body, rhythmically layered in its lower part (the Layered Complex) and indistinctly layered and enriched in eudialyte-group minerals in its upper part (the Eudialyte Complex). The Eudialyte Complex is composed of two groups of rocks. Among the hypersolvus meso-melanocratic alkaline rocks (mainly malignite, as well as shonkinite, melteigite, and ijolite enriched with the eudialyte-group minerals, EGM), there are lenses of subsolvus leucocratic rocks (foyaite, fine-grained nepheline syenite, urtite with phosphorus mineralization, and primary lovozerite-group minerals). Leucocratic rocks were formed in the process of the fractional crystallization of melanocratic melt enriched in Fe, high field strength elements (HFSE), and halogens. The fractionation of the melanocratic melt proceeded in the direction of an enrichment in nepheline and a decrease in the aegirine content. A similar fractionation path occurs in the Na2O-Al2O3-Fe2O3-SiO2 system, where the melt of the “ijolite” type (approximately 50% of aegirine) evolves towards “phonolitic eutectic” (approximately 10% of aegirine). The temperature of the crystallization of subsolvus leucocratic rocks was about 550 °C. Hypersolvus meso-melanocratic rocks were formed at temperatures of 700–350 °C, with a gradual transition from an almost anhydrous HFSE-Fe-Cl/F-rich alkaline melt to a Na(Cl, F)-rich water solution. Devonian volcaniclastic rocks underwent metasomatic treatment of varying intensity and survived in the Eudialyte Complex, some remaining unchanged and some turning into nepheline syenites. In these rocks, there are signs of a gradual increase in the intensity of alkaline metasomatism, including a wide variety of zirconium phases. The relatively high fugacity of fluorine favored an early formation of zircon in apo-basalt metasomatites. The ensuing crystallization of aegirine in the metasomatites led to an increase in alkali content relative to silicon and parakeldyshite formation. After that, EGM was formed, under the influence of Ca-rich solutions produced by basalt fenitization.

scholarly journals Eudialyte Group Minerals from the Lovozero Alkaline Massif, Russia: Occurrence, Chemical Composition, and Petrogenetic Significance

Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1070
Author(s):  
Julia A. Mikhailova ◽  
Yakov A. Pakhomovsky ◽  
Taras L. Panikorovskii ◽  
Ayya V. Bazai ◽  
Victor N. Yakovenchuk
Keyword(s):  
Chemical Composition ◽  
Nepheline Syenite ◽  
Granite Gneiss ◽  
Lovozero Massif ◽  
Eudialyte Group ◽  
Magmatic Stage ◽  
Late Magmatic Stage ◽  
Volcaniclastic Rocks ◽  
Layered Complex ◽  
Alkaline Massif

The Lovozero Alkaline Massif intruded through the Archean granite-gneiss and Devonian volcaniclastic rocks ca. 360 Ma ago and formed a large laccolith-type body. The lower part of the massif (the Layered complex) is composed of regularly repeating rhythms: melanocratic nepheline syenite (lujavrite, at the top), leucocratic nepheline syenite (foyaite), foidolite (urtite). The upper part of the massif (the Eudialyte complex) is indistinctly layered, and lujavrite enriched with eudialyte-group minerals (EGM) prevails there. In this article, we present the results of a study of the chemical composition and petrography of more than 400 samples of the EGM from the main types of rock of the Lovozero massif. In all types of rock, the EGM form at the late magmatic stage later than alkaline clinopyroxenes and amphiboles or simultaneously with it. When the crystallization of pyroxenes and EGM is simultaneous, the content of ferrous iron in the EGM composition increases. The Mn/Fe ratio in the EGM increases during fractional crystallization from lujavrite to foyaite and urtite. The same process leads to an increase in the modal content of EGM in the foyaite of the Layered complex and to the appearance of primary minerals of the lovozerite group in the foyaite of the Eudialyte complex.

Eudialyte-group minerals in rocks of Lovozero layered complex at Mt. Karnasurt and Mt. Kedykvyrpakhk

2015 ◽  
Vol 57 (7) ◽  
pp. 600-613 ◽  
Author(s):  
G. Yu. Ivanyuk ◽  
Ya. A. Pakhomovsky ◽  
V. N. Yakovenchuk
Keyword(s):  
Eudialyte Group ◽  
Layered Complex

scholarly journals Stratigraphy and lithogeochemistry of the Goldenville horizon and associated rocks, Baie Verte Peninsula, Newfoundland

2021 ◽  
Author(s):  
C Mueller ◽  
S J Piercey ◽  
M G Babechuk ◽  
D Copeland
Keyword(s):  
Gold Mineralization ◽  
Iron Formation ◽  
Fine Grained ◽  
Hydrothermal Sediment ◽  
Post Archean Australian Shale ◽  
Oxygenated Water ◽  
Volcaniclastic Rocks ◽  
Laurentian Margin ◽  
Mn Oxides ◽  
Hydrothermal Venting

The Goldenville horizon in the Baie Verte Peninsula is an important stratigraphic horizon that hosts primary (Cambrian to Ordovician) exhalative magnetite and pyrite and was a chemical trap for younger (Silurian to Devonian) orogenic gold mineralization. The horizon is overlain by basaltic flows and volcaniclastic rocks, is intercalated with variably coloured argillites and cherts, and underlain by mafic volcaniclastic rocks; the entire stratigraphy is cut by younger fine-grained mafic dykes and coarser gabbro. Lithogeochemical signatures of the Goldenville horizon allow it to be divided into high-Fe iron formation (HIF; >50% Fe2O3), low-Fe iron formation (LIF; 15-50% Fe2O3), and argillite with iron minerals (AIF; <15% Fe2O3). These variably Fe-rich rocks have Fe-Ti-Mn-Al systematics consistent with element derivation from varying mineral contributions from hydrothermal venting and ambient detrital sedimentation. Post-Archean Australian Shale (PAAS)-normalized rare earth element (REE) signatures for the HIF samples have negative Ce anomalies and patterns similar to modern hydrothermal sediment deposited under oxygenated ocean conditions. The PAAS-normalized REE signatures of LIF samples have positive Ce anomalies, similar to hydrothermal sediment deposited under anoxic to sub-oxic conditions. The paradoxical Ce behaviour is potentially explained by the Mn geochemistry of the LIF samples. The LIF have elevated MnO contents (2.0-7.5 weight %), suggesting that Mn from hydrothermal fluids was oxidized in an oxygenated water column during hydrothermal venting, Mn-oxides then scavenged Ce from seawater, and these Mn-oxides were subsequently deposited in the hydrothermal sediment. The Mn-rich LIF samples with positive Ce anomalies are intercalated with HIF with negative Ce anomalies, both regionally and on a metre scale within drill holes. Thus, the LIF positive Ce anomaly signature may record extended and particle-specific scavenging rather than sub-oxic/redox-stratified marine conditions. Collectively, results suggest that the Cambro-Ordovician Taconic seaway along the Laurentian margin may have been completely or near-completely oxygenated at the time of Goldenville horizon deposition.

Sergevanite, Na15(Ca3Mn3)(Na2Fe)Zr3Si26O72(OH)3·H2O, a new eudialyte-group mineral from the Lovozero alkaline massif, Kola Peninsula

2020 ◽  
Vol 58 (4) ◽  
pp. 421-436 ◽  
Author(s):  
Nikita V. Chukanov ◽  
Sergey M. Aksenov ◽  
Igor V. Pekov ◽  
Dmitriy I. Belakovskiy ◽  
Svetlana A. Vozchikova ◽  
...  
Keyword(s):  
Kola Peninsula ◽  
Structural Data ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Calculated Density ◽  
Eudialyte Group ◽  
Group Mineral ◽  
X Ray ◽  
Mohs Hardness ◽  
Alkaline Massif

ABSTRACT The new eudialyte-group mineral sergevanite, ideally Na15(Ca3Mn3)(Na2Fe)Zr3Si26O72(OH)3·H2O, was discovered in highly agpaitic foyaite from the Karnasurt Mountain, Lovozero alkaline massif, Kola Peninsula, Russia. The associated minerals are microcline, albite, nepheline, arfvedsonite, aegirine, lamprophyllite, fluorapatite, steenstrupine-(Ce), ilmenite, and sphalerite. Sergevanite forms yellow to orange-yellow anhedral grains up to 1.5 mm across and the outer zones of some grains of associated eudialyte. Its luster is vitreous, and the streak is white. No cleavage is observed. The Mohs' hardness is 5. Density measured by equilibration in heavy liquids is 2.90(1) g/cm3. Calculated density is equal to 2.906 g/cm3. Sergevanite is nonpleochroic, optically uniaxial, positive, with ω = 1.604(2) and ε = 1.607(2) (λ = 589 nm). The infrared spectrum is given. The chemical composition of sergevanite is (wt.%; electron microprobe, H2O determined by HCN analysis): Na2O 13.69, K2O 1.40, CaO 7.66, La2O3 0.90, Ce2O3 1.41, Pr2O3 0.33, Nd2O3 0.64, Sm2O3 0.14, MnO 4.15, FeO 1.34, TiO2 1.19, ZrO2 10.67, HfO2 0.29, Nb2O5 1.63, SiO2 49.61, SO3 0.77, Cl 0.23, H2O 4.22, –O=Cl –0.05, total 100.22. The empirical formula (based on 25.5 Si atoms pfu, in accordance with structural data) is H14.46Na13.64K0.92Ca4.22Ce0.27La0.17Nd0.12Pr0.06Sm0.02Mn1.81Fe2+0.58Ti0.46Zr2.67Hf0.04Nb0.38Si25.5S0.30Cl0.20O81.35. The crystal structure was determined using single-crystal X-ray diffraction data. The new mineral is trigonal, space group R3, with a = 14.2179(1) Å, c = 30.3492(3) Å, V = 5313.11(7) Å3, and Z = 3. In the structure of sergevanite, Ca and Mn are ordered in the six-membered ring of octahedra (at the sites M11 and M12), and Na dominates over Fe2+ at the M2 site. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 7.12 (70) (110), 5.711 (43) (202), 4.321 (72) (205), 3.806 (39) (033), 3.551 (39) (220, 027), 3.398 (39) (313), 2.978 (95) (), 2.855 (100) (404). Sergevanite is named after the Sergevan' River, which is near the discovery locality.

Composition, technology and provenance of Roman pottery fromNapoca(Cluj-Napoca, Romania)

Clay Minerals ◽  
2018 ◽  
Vol 53 (4) ◽  
pp. 621-641 ◽  
Author(s):  
Ágnes Gál ◽  
Corina Ionescu ◽  
Mátyás Bajusz ◽  
Vlad A. Codrea ◽  
Volker Hoeck ◽  
...  
Keyword(s):  
Middle Miocene ◽  
Raw Materials ◽  
Ceramic Body ◽  
Polarized Light ◽  
Raw Material ◽  
Gradual Transition ◽  
X Ray ◽  
Fine Grained ◽  
The Matrix ◽  
Technological Constraints

ABSTRACTSecond-century CE (common era) household pottery sherds found in the city ofNapoca(present day Cluj-Napoca, Romania) in Roman Dacia were investigated by polarized light optical microscopy, X-ray powder diffraction, Fourier-transform infrared spectroscopy and cold field emission scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy to obtain information on technology, raw materials and site of production. Compositionally, all samples are similar with comparable fine and semi-fine microstructures and oriented microtextures. Optically, there is a gradual transition from microcrystalline to an amorphous illitic-muscovitic matrix. The small aplastic inclusions are mostly quartz and feldspar. Fine-grained carbonate aggregates are distributed inhomogeneously in the ceramic body. Well-preserved Middle Miocene foraminifera tests are characteristic of the ceramics. The gradual thermal changes of the matrix and the newly formed phases upon firing, such as ‘ceramic melilite’, Fe-gehlenite, clinopyroxene, glass, hematite and some maghemite support inferences regarding the technological constraints in producing the pottery. The firing took place in a mostly oxidizing atmosphere and the temperature extended from at least 850°C to >900°C. The Middle Miocene marly clay from the area surrounding the site shows similar mineralogical and micropalaeontological contents to those of the ceramic specimens and is the best candidate for the raw material used for local production of the Roman pottery.

scholarly journals Na-dominant (at the M2 site) eudialyte analogue: crystal structure and indicatory significance

2020 ◽  
Vol 9 ◽  
pp. 19-25
Author(s):  
R. K. Rastsvetaeva ◽  
◽  
N. V. Chukanov ◽  
Ch. Schäfer ◽  
Keyword(s):  
Crystal Structure ◽  
Electron Probe ◽  
New Mineral ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Eudialyte Group ◽  
X Ray ◽  
Cell Parameters ◽  
Atomic Displacements ◽  
Alkaline Massif

Minerals of the eudialyte group from ultra-agpaitic associations are often characterized by high contents (up to the dominance) of sodium at the M2 site, which is populated with iron in eudialyte. The features of blocky isomorphism with the replacement of IVFe2+ by IVNa and VNa at the M2 micro-region are discussed. Using the methods of electron probe microanalysis, X-ray diffraction and IR spectroscopy, a potentially new mineral, M2Na-dominant analogue of eudialyte from the Ilimaussaq alkaline massif (Greenland), was investigated. Its crystal structure was refined to R = 5.6 % in the anisotropic approximation of atomic displacements using 1095 independent reflections with F > 3(F). The unit-cell parameters are: a = 14.208(1), c = 30.438(1) Å, V = 5321(1) Å3; the space group is R-3m. The idealized formula of the mineral is (Z = 3): (Na,H3O)15Ca6Zr3[Na2Fe][Si26O72](OH)2Cl∙2H2O.

Submarine-fan characteristics and dual sediment provenance, Lower Carboniferous Bragdon Formation, eastern Klamath terrane, California

1989 ◽  
Vol 26 (5) ◽  
pp. 927-940 ◽  
Author(s):  
M. Meghan Miller ◽  
Bingquan Cui
Keyword(s):  
Early Carboniferous ◽  
Sediment Provenance ◽  
Dispersal Pattern ◽  
Submarine Fan ◽  
Lower Carboniferous ◽  
Sediment Dispersal ◽  
Fine Grained ◽  
Rock Fragments ◽  
Western Cordillera ◽  
Volcaniclastic Rocks

The Carboniferous Bragdon Formation comprises sandstone, argillite, and conglomerate, which were deposited in a hybrid submarine-fan setting. The Bragdon Formation contains a crudely progradational succession of sand-rich turbidites and intercalated channel fill and debris flows. Apparent paucity of fine-grained rocks and relatively high sedimentation rates may suggest deposition within a small, rapidly subsiding, ponded basin. Three end-member petrologic sandstone types include (i) quartz-rich, chert-rich, and sedimentary-lithic-rich sandstone, (ii) volcanic-lithic- and feldspar-rich sandstone, and (iii) crystal-rich sandstone and tuffaceous argillite. The compositions reflect basement uplift, arc dissection, and the persistence of volcanism, respectively. Interbedded strata of differing provenance, together with little or no provenance mixing within beds, indicate multicomponent source terranes, line-source sediment dispersal pattern, and limited transport distances.Facies associations and provenance together suggest extension or transtension within an arc-related basinal setting during the Late Devonian and Early Carboniferous, resulting in deposition of epiclastic sediments that were rich in sedimentary rock fragments in a Paleozoic succession otherwise dominated by volcaniclastic rocks or fringing carbonates. Mid-Paleozoic chert-rich epiclastic strata are widespread within the western Cordillera in a variety of tectonic regimes that may be broadly related to the same oblique plate margin.

scholarly journals Agpaitic Alkaline Rocks in Southern Brazilian Platform: A Review

Minerals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 934
Author(s):  
Celso de Barros Gomes ◽  
Rogério Guitarrari Azzone ◽  
Gaston Eduardo Enrich Rojas ◽  
Vincenza Guarino ◽  
Excelso Ruberti
Keyword(s):  
South America ◽  
General Information ◽  
Early Triassic ◽  
Southern Brazil ◽  
Fine Grained ◽  
Mineral Assemblages ◽  
Magmatic Stage ◽  
Poços De Caldas ◽  
Late Magmatic Stage ◽  
Alkaline Massif

General information is presented on ten agpaitic occurrences located in southern Brazil and at the border between Brazil and Paraguay. All the Brazilian agpaitic rocks are Late Cretaceous in age, whereas the Paraguayan ones are older than Early Triassic. The most significant occurrence is Poços de Caldas, the largest alkaline massif in South America. In general, these agpaitic rocks contain mineral assemblages that indicate presence of typical halogen-bearing Na–Ca–HFSE phases, eudialyte-, rinkite- and wöhlerite-group minerals being the most frequent ones. However, these associations are indeed more complex in terms of composition, with accessory phases in some cases consisting of various minerals, including U–Th oxides/silicates, Nb oxides, REE–Sr–Ba bearing carbonates–fluorocarbonates–phosphates–silicates and Zr–Na rich silicates. They usually form late magmatic stage to hydrothermal/deuteric assemblages linked with coarse and fine-grained, mainly silica-undersaturated evolved rocks. Data also indicate significant differences in type, amount and composition of agpaitic minerals in all investigated occurrences.

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