Search Results (22)

This article presents the results of fractal texture analyses of selected minerals (aegirine, eudialyte, orthoclase) in the northwestern part of the Lovozero intrusion. This intrusion is located in northeastern Scandinavia and is a massif made of alkaline rocks. There are rocks such as massive syenites and porphyrtes, as well as iiolites, urtites, and foyaites, accompanied by metasomatic rocks of the contact zone. A box-counting fractal dimension was used to numerically represent the texture of these minerals. In the further part, this coefficient was visualized in the form of maps superimposed on the study area, and some simple arithmetic calculations were performed to highlight the common features of this dimension for the selected rock-forming minerals. In conjunction with the geological interpretation of these results, rock-forming processes in this massif were depicted. This work is preliminary, showing the potential of this calculation method in petrological applications. Full article

Berthierine was found in a natrolite vein intersecting volcanogenic-sedimentary rocks on the slope of Mt. Quamdespakh in the upper reaches of the Suolwai River, Lovozero alkaline massif, Kola peninsula, Russian Arctic. The mineral occurs as well-formed translucent pyramidal crystals up to 250 μm in size. The chemical composition determined by electron microprobe analysis corresponds to the empirical formula ^VI(Fe²⁺_1.99Al_0.94Mg_0.03Mn_0.04)_Σ3.00[^IV(Si_1.15Al_0.85)_Σ2.00O₅] [(OH)_3.92O_0.08]_Σ4.00; the idealized formula is ^VI(Fe²⁺₂Al)[^IV(SiAl)O₅](OH)₄. The crystal-structure determination (the first detailed crystal-structure characterization of berthierine) shows that the Lovozero mineral is hexagonal, P6₃cm (a = 5.3903(4), c = 14.0146(10) Å, V = 352.64(6) ų, R₁ = 0.053 for 338 unique observed reflections), and corresponds to the 2H₁ polytype of serpentine-group minerals with 1:1 tetrahedral-octahedral layers. The unit cell contains two M₃[T₂O₅](OH)₄ layers (M = Fe²⁺,Al; T = Si,Al) stacked along the c axis. The calculations of information-based structural and topological complexity parameters indicate that berthierine is structurally and topologically simpler than its chlorite-group polymorph chamosite. Since berthierine usually crystallizes metastably in the stability field of chamosite, the complexity analysis is agreement with the Goldsmith rule that states that, in Ostwald sequences of crystallization, metastable phases are simpler and more disordered than their stable counterparts. This observation can be applied to a general case of the metastable formation of serpentine-group minerals prior to the crystallization of chlorites. Full article

A comprehensive study (monitoring, thermodynamic modeling) of natural and anthropogenically polluted waters of the Lovozero Massif has been carried out. A thermodynamic study of the weathering of the Lovozero Massif within the “water-rock-atmosphere” system at a temperature of 5 °C showed that the elements contained in the rocks of the studied massif influence the formation of the chemical composition of natural waters. It has been established that an increase in the degree of “water-rock” interaction leads to an increase in the concentrations of F⁻, Cl⁻, SO₄²⁻, and HCO₃⁻ in the solution. This affects the mobility of lanthanum, cerium, and other elements due to the formation of complex compounds with them. The relatively high content of fluorine, phosphorus, and HCO₃⁻ (weak and medium acids) in the solution promotes the dissolution of silicates while Si, Al, and P are released into the solution. Monitoring of water from a flooded mine in which there is an increase in the degree of interaction of water with rock showed higher pH values for the concentrations of Na, HCO₃⁻, F⁻, P, Al, Si, V, U, La, and Ce. The conclusions are relevant in the context of the use of groundwater for drinking water supply purposes. The obtained information is useful to evaluate the health of the population of the region under study. Full article

The 360–370 Ma old Lovozero massif (NW Russia) is a layered nepheline syenitic-foidolitic pluton. Despite its huge size (650 km²), the massif is surrounded by a narrow fenite aureole, and the most intensive fenitization is associated with pegmatites and hydrothermal veins that have intruded into the wall rocks. We studied petrography, petrochemistry, mineralogy and fluid inclusions along a profile crossing the direct contact of the Lovozero massif with country Archean gneiss. We found that the fluid responsible for fenitization was a heterogeneous mixture of two coexisting phases, an aqueous fluid with salinity 8.6–15.1 eq. wt.% NaCl and a methane fluid. The coexistence of these two fluids indicates immiscibility conditions at (or below) CH₄–H₂O solvus. The aqueous fluid affected both the endocontact alkaline rocks and country gneiss. In the endocontact, intense autometasomatic alterations of the early crystallized minerals occurred, for example, the natrolitization of nepheline and sodalite. Besides, the aqueous fluid transported Na₂O, K₂O, as well as P₂O₅, TiO₂, H₂O, F, Cl and S into the exocontact. These components were precipitated in the immediate vicinity of the massif contact, and the salinity of the aqueous fluid decreased to 0.53–3.06 eq. wt.% NaCl. We assume that there are two reasons for a narrow fenite aureole in the Lovozero massif: intense autometasomatic alterations and a decrease in the permeability of country rocks due to fluid immiscibility. Full article

Nepheline, ideally Na₃K(Al₄Si₄O₁₆) is a key mineral of silica-undersaturated igneous rocks. Under subsolidus conditions, nepheline is intensively replaced by numerous secondary minerals, of which various zeolites (mainly natrolite, analcime, gonnardite), as well as cancrinite, muscovite and Al-O-H phases (gibbsite, böhmite, nordstrandite) are the most common. In the rocks of the Lovozero alkaline massif (Kola Peninsula, NW Russia), nepheline is extensively replaced by the association natrolite + nordstrandite ± böhmite ± paranatrolite. To reproduce the conditions for the formation of such a mineral association, a series of experiments were carried out on the dissolution of nepheline in deionized water, 0.5 mol/L NaCl, 0.5 mol/L NaOH, and 0.1 mol/L HCl at 230 °C for 1/5/15 days. When nepheline is partially dissolved, phases and mixtures of phases precipitate on the surface of its grains, and these phases were diagnosed using X-ray powder diffraction and Raman spectroscopy. Observations in natural samples and experimental studies have shown that the nepheline alteration in the rocks of the Lovozero massif with the formation of natrolite and Al-O-H phases occurred under the influence of a high to medium salinity solution at a pH of near 6. Full article

Polymineralic inclusions in loparite-(Ce) in alkaline rocks from the Lovozero massif (Russia) were investigated using electron microprobe analysis, Raman spectroscopy, and X-ray diffraction. A total of 21 mineral species and two groups of minerals (pyrochlore- and labuntsovite-group minerals) were found in these inclusions. Minerals in loparite-hosted inclusions can be divided into two groups: (1) minerals found typically in rocks bearing loparite-(Ce) grains (groundmass minerals) such as aegirine, magnesio-arfvedsonite, potassic feldspar, albite, fluorapatite, etc.; and (2) minerals that were not found in the rock outside of the loparite-(Ce) grains. The latter include lorenzenite, labuntsovite-group minerals, minerals of the neptunite–manganoneptunite series, vinogradovite, catapleiite, fluorite, britholite-(Ce), barylite, genthelvite, and barite, found in the studied samples exclusively inside loparite-(Ce) crystals. The minerals of the second group are typical hydrothermal minerals. We assume that the skeletal crystals of loparite-(Ce), when growing, captured both co-crystallizing minerals and small drops of the mineral-forming solution. Such drops subsequently crystallized within the loparite-(Ce), resulting in the formation of a hydrothermal mineral association. Full article

The crystal structure of manganotychite has been refined using the holotype specimen from the Alluaiv Mountain, Lovozero massif, Kola peninsula, Russia. The mineral is cubic, Fd$\overline{3}$, a = 14.0015(3) Å, V = 2744.88(18) ų, Z = 8, R₁ = 0.020 for 388 independently observed reflections. Manganotychite is isotypic to tychite and ferrotychite. Its crystal structure is based upon a three-dimensional infinite framework formed by condensation of MnO₆ octahedra and CO₃ groups by sharing common O atoms. The sulfate groups and Na⁺ cations reside in the cavities of the octahedral-triangular metal-carbonate framework. In terms of symmetry and basic construction of the octahedral-triangular framework, the crystal structure of manganotychite is identical to that of northupite, Na₃Mg(CO₃)₂Cl. The transition northupite → tychite can be described as a result of the multiatomic 2Cl⁻ → (SO₄)²⁻ substitution, where both chlorine and sulfate ions are the extra-framework constituents. However, the positions occupied by sulfate groups and chlorine ions correspond to different octahedral cavities within the skeletons of Na atoms. The crystal structure of northupite can be considered as an interpenetration of two frameworks: anionic [Mg(CO₃)₂]²⁻ octahedral-triangular framework and cationic [ClNa₃]²⁻ framework with the antipyrochlore topology. Both manganotychite and northupite structure types can be described as a modification of the crystal structure of diamond (or the dia net) via the following steps: (i) replacement of a vertex of the dia net by an M₄ tetrahedron (no symmetry reduction); (ii) attachment of (CO₃) triangles to the triangular faces of the M₄ tetrahedra (accompanied by the Fd$\overline{3}$m → Fd$\overline{3}$ symmetry reduction); (iii) filling voids of the resulting framework by Na⁺ cations (no symmetry reduction); and (iv) filling voids of the Na skeleton by either sulfate groups (in tychite-type structures) or chlorine atoms (in northupite). As a result, the information-based structural complexity of manganotychite and northupite exceeds that of the dia net. Full article

The 360-370-Ma-old Lovozero peralkaline massif (NW Russia) is a layered nepheline syenitic–foidolitic pluton. In the rocks of the massif, late-stage (auto)metasomatic alterations of rock-forming minerals are quite intense. We studied the products of the alteration of nepheline and sodalite via microtextural, microprobe, and spectroscopic methods. We found that these minerals are extensively replaced by the association between natrolite + nordstrandite ± böhmite ± paranatrolite in accordance with the following reactions: 3Nph + 4H₂O → Ntr + Nsd + NaOH; 6Nph + 9H₂O → Ntr + Pntr + 2Nsd + 2NaOH; Sdl + 4H₂O → Ntr + Nsd + NaOH + NaCl, where Nph is nepheline, Ntr is natrolite, Nsd is nordstrandite, Pntr is paranatrolite, and Sdl is sodalite. As a result, about one-third of the sodium from nepheline (and sodalite) is set free and passes into the fluid. This leads to an increase in the Na/Cl ratio and, hence, the pH of the fluid. An increase in pH stabilizes hyperagpaitic minerals (e.g., ussingite, villiaumite, thermonatrite, and trona), which can crystallize in close proximity to pseudomorphized nepheline and sodalite. Thus, the alteration of feldspathoids increases the pH of late-magmatic fluids, which in turn can lead to the crystallization of hyperagpaitic minerals. Full article

Eudialyte-group minerals (EGMs) are typical accessory or rock-forming minerals of the Lovozero peralkaline massif (Kola Peninsula, Russia). The EGM grains in the rocks of the massif are often replaced by an association of various secondary minerals such as lovozerite and wöhlerite group minerals, as well as terskite, catapleiite, elpidite, gaidonnayite, vlasovite, zircon, and loparite-(Ce). However, EGMs in the Lovozero massif can be not only pseudomorphized, but also partially or completely dissolved. The partial dissolution of eudialyte grains was simulated in three series of experiments, and the results obtained were compared with natural samples. Observations in natural samples and experimental studies have shown that the partial dissolution of eudialyte-group minerals occurs in two stages: (1) loss of sodium and hydration; (2) loss of other cations not included in the zirconosilicate framework. This process proceeds most intensively in acidic hydrothermal solutions and may be responsible for the appearance of new mineral species in the eudialyte group. Full article

Nepheline is a nominally anhydrous aluminosilicate that typically contains an impurity of ferric iron replacing aluminum in tetrahedral sites. However, previous researchers noted the constant presence of ferrous iron in the chemical composition of nepheline from the rocks of the Khibiny and Lovozero massifs (Kola Peninsula, Russia). We have carried out microprobe, spectroscopic, chemical and crystal chemical studies of nepheline from the Lovozero massif. We have established the presence of molecular water in nepheline, and also that the incorporation of ferrous iron into nepheline crystal structure is associated with the simultaneous increasing of the coordination number from four to five (or six) due to the inclusion of the ‘additional’ water molecules that form point [FeO₄(H₂O)_n]-defects (where n = 1, 2) in the tetrahedral framework. The nepheline iron content is closely related to the presence of small needle-like aegirine inclusions. The total iron content in nepheline saturated with aegirine needles is approximately an order of magnitude lower than in nepheline free from aegirine inclusions. Most likely the aegirine inclusions in nepheline are formed as a result of the decomposition of the nepheline–“iron nepheline” solid solution. We propose that this process is triggered by the oxidation of ferrous iron in the crystal structure of nepheline. Full article

In the Khibiny and Lovozero alkaline massifs, there are numerous xenoliths of the so-called ‘aluminous hornfelses’ composed of uncommon mineral associations, which, firstly, are ultra-aluminous, and secondly, are highly reduced. (K,Na)-feldspar, albite, hercynite, fayalite, minerals of the phlogopite-annite and cordierite-sekaninaite series, corundum, quartz, muscovite, sillimanite, and andalusite are rock-forming minerals. Fluorite, fluorapatite, ilmenite, pyrrhotite, ulvöspinel, troilite, and native iron are characteristic accessory minerals. The protolith of these rocks is unknown. We studied in detail the petrography, mineralogy, and chemical composition of these rocks and believe that hornfelses were formed as a result of the metasomatic influence of foidolites. The main reason for the formation of an unusual aluminous association is the high mobility of aluminum promoted by the formation of fluid expelled from foidolites of the Na-Al-OH-F complexes. Thus, it is fluorine that controls the mobility of aluminum in the fluid and, consequently, the mineral associations of alkaline metasomatites. The gain of alkalis and aluminum to rocks of protolith was the reason for the intense crystallization of (K,Na)-feldspar. As a result, a SiO₂ deficiency was formed, and Si-poor, Al-rich silicates and/or oxides crystallized. Full article

Eudialyte-group minerals are important accessory minerals of peralkaline rocks of nepheline-syenite massifs and alkaline–ultramafic complexes. Here, we report the complex study of a eudialyte-group mineral (EGM) from peralkaline pegmatite of the alkaline-ultrabasic Odikhincha massif (Polar Siberia). The chemical composition of the studied EGM is intermediate between those of taseqite and eudialyte, with small admixtures of other members of the eudialyte group. The crystals of EGMs were formed during the postmagmatic stage in the temperature range of 300–350 °C and partly replaced by late eudialite along cracks during the zeolite stage (~230 °C). The chemical compositions, structural features and mineral association of the studied EGM are similar to those of Sr-Nb-dominant EGM found in other nepheline-syenite massifs, such as Khibiny, Lovozero and Pilansberg. The EGM studied in this work is a Cl-deficient taseqite variety (“monochlore taseqite”), which differs from “dichlorotaseqite” (found only in the Ilimaussaq massif) by a lower amount of chlorine. Full article

This manuscript deals with the analysis of significant rare earth elements (REE) minerals such as eudialyte, lorenzenite, loparite, perovskite, titanite, apatite, and carbonates. These minerals are found in the rocks of the Khibiny, Lovozero, Afrikanda, and Kovdor massifs (the Paleozoic hotspot activity in the Kola-Karelian Alkaline Province is estimated at about 100,000 km²). Performed microscopic analyses that demonstrated their structure and optical features (dimming, interference colors, relief). Single-crystal analysis using XRD methods, SEM-EDS, and spectroscopic (FTIR) studies allowed the characteristics of described minerals: Lorenzenite in Lovozero probably crystalized after loparite have small additions of Nb, La, Ce, Pr, and Nd. Loparite and perovskite have the addition of Ce, Nb, and Ta. The same dopants have titanite probably crystalized after perovskite. Calcite in these massifs had the addition of Ce and Sr, the same as in fluorapatite, which was found in these rocks too. All of the analyzed minerals are REE-bearing and can be considered as deposits. Full article

The Lovozero peralkaline massif (Kola Peninsula, Russia) has several deposits of Zr, Nb, Ta and rare earth elements (REE) associated with eudialyte-group minerals (EGM). Eudialyte from the Alluaiv Mt. often forms zonal grains with central parts enriched in Zr (more than 3 apfu) and marginal zones enriched in REEs. The detailed study of the chemical composition (294 microprobe analyses) of EGMs from the drill cores of the Mt. Alluaiv-Mt. Kedykvyrpakhk deposits reveal more than 70% Zr-enriched samples. Single-crystal X-ray diffraction (XRD) was performed separately for the Zr-rich (4.17 Zr apfu) core and the REE-rich (0.54 REE apfu) marginal zone. It was found that extra Zr incorporates into the octahedral M1A site, where it replaces Ca, leading to the symmetry lowering from R$\overline{3}$m to R32. We demonstrated that the incorporation of extra Zr into EGMs makes the calculation of the eudialyte formula on the basis of Si + Al + Zr + Ti + Hf + Nb + Ta + W = 29 apfu inappropriate. Full article

The Lovozero peralkaline massif (Kola Peninsula, Russia) is widely known for its unique mineral diversity, and most of the rare metal minerals are found in pegmatites, which are spatially associated with poikilitic rocks (approximately 5% of the massif volume). In order to determine the reasons for this relationship, we have investigated petrography and the chemical composition of poikilitic rocks as well as the chemical composition of the rock-forming and accessory minerals in these rocks. The differentiation of magmatic melt during the formation of the rocks of the Lovozero massif followed the path: lujavrite → foyaite → urtite (magmatic stage) → pegmatite (hydrothermal stage). Yet, for peralkaline systems, the transition between magmatic melt and hydrothermal solution is gradual. In the case of the initially high content of volatiles in the melt, the differentiation path was probably as follows: lujavrite → foyaite (magmatic stage) → urtitization of foyaite → pegmatite (hydrothermal stage). Poikilitic rocks were formed at the stage of urtitization, and we called them pre-pegmatites. Indeed, the poikilitic rocks have a metasomatic texture and, in terms of chemical composition, correspond to magmatic urtite. The reason for the abundance of rare metal minerals in pegmatites associated with poikilitic rocks is that almost only one nepheline is deposited during urtitization, whereas during the magmatic crystallization of urtite, rare elements form accessory minerals in the rock and are less concentrated in the residual solution. Full article