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Keywords = peralkaline nepheline syenites

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20 pages, 5522 KiB  
Review
Rare Earth Element Deposits in Mongolia
by Jaroslav Dostal and Ochir Gerel
Minerals 2023, 13(1), 129; https://doi.org/10.3390/min13010129 - 16 Jan 2023
Cited by 11 | Viewed by 11425
Abstract
In Mongolia, rare earth element (REE) mineralization of economic significance is related either to the Mesozoic carbonatites or to the Paleozoic peralkaline granitoid rocks. Carbonatites occur as part of alkaline silicate-carbonatite complexes, which are composed mainly of nepheline syenites and equivalent volcanic rocks. [...] Read more.
In Mongolia, rare earth element (REE) mineralization of economic significance is related either to the Mesozoic carbonatites or to the Paleozoic peralkaline granitoid rocks. Carbonatites occur as part of alkaline silicate-carbonatite complexes, which are composed mainly of nepheline syenites and equivalent volcanic rocks. The complexes were emplaced in the Gobi-Tien Shan rift zone in southern Mongolia where carbonatites usually form dikes, plugs or intruded into brecciated rocks. In mineralized carbonatites, REE occur mainly as fluorocarbonates (bastnäsite, synchysite, parisite) and apatite. Apatite is also present in the carbonatite-hosted apatite-magnetite (mostly altered to hematite) bodies. Alkaline silicate rocks and carbonatites show common geochemical features such as enrichment of light REE but relative depletion of Ti, Zr, Nb, Ta and Hf and similar Sr and Nd isotopic characteristics suggesting the involvement of the heterogeneous lithospheric mantle in the formation of both carbonatites and associated silicate rocks. Hydrothermal fluids of magmatic origin played an important role in the genesis of the carbonatite-hosted REE deposits. The REE mineralization associated with peralkaline felsic rocks (peralkaline granites, syenites and pegmatites) mainly occurs in Mongolian Altai in northwestern Mongolia. The mineralization is largely hosted in accessory minerals (mainly elpidite, monazite, xenotime, fluorocarbonates), which can reach percentage levels in mineralized zones. These rocks are the results of protracted fractional crystallization of the magma that led to an enrichment of REE, especially in the late stages of magma evolution. The primary magmatic mineralization was overprinted (remobilized and enriched) by late magmatic to hydrothermal fluids. The mineralization associated with peralkaline granitic rocks also contains significant concentrations of Zr, Nb, Th and U. There are promising occurrences of both types of rare earth mineralization in Mongolia and at present, three of them have already established significant economic potential. They are mineralization related to Mesozoic Mushgai Khudag and Khotgor carbonatites in southern Mongolia and to the Devonian Khalzan Buregtei peralkaline granites in northwestern Mongolia. Full article
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20 pages, 5105 KiB  
Article
Alteration of Feldspathoids Changes pH of Late-Magmatic Fluids: A Case Study from the Lovozero Peralkaline Massif, Russia
by Julia A. Mikhailova, Yakov A. Pakhomovsky, Lyudmila M. Lyalina and Ekaterina A. Selivanova
Minerals 2023, 13(1), 39; https://doi.org/10.3390/min13010039 - 26 Dec 2022
Cited by 3 | Viewed by 2168
Abstract
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 [...] Read more.
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
(This article belongs to the Special Issue Isomorphism and Solid Solutions of Minerals and Related Compounds)
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19 pages, 3988 KiB  
Article
Chlorine-Deficient Analog of Taseqite from Odikhincha Massif (Russia): Genesis and Relation with Other Sr-Rich Eudialyte-Group Minerals
by Victor A. Zaitsev, Nikita V. Chukanov and Sergey M. Aksenov
Minerals 2022, 12(8), 1015; https://doi.org/10.3390/min12081015 - 12 Aug 2022
Cited by 1 | Viewed by 2016
Abstract
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 [...] Read more.
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 article belongs to the Special Issue Study of the Eudialyte Group Minerals)
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14 pages, 4639 KiB  
Article
Compositional Variation of Eudialyte-Group Minerals from the Lovozero and Ilímaussaq Complexes and on the Origin of Peralkaline Systems
by Lia N. Kogarko and Troels F. D. Nielsen
Minerals 2021, 11(6), 548; https://doi.org/10.3390/min11060548 - 21 May 2021
Cited by 8 | Viewed by 2603
Abstract
The Lovozero complex, Kola peninsula, Russia and the Ilímaussaq complex in Southwest Greenland are the largest known layered peralkaline intrusive complexes. Both host world-class deposits rich in REE and other high-tech elements. Both complexes expose spectacular layering with horizons rich in eudialyte group [...] Read more.
The Lovozero complex, Kola peninsula, Russia and the Ilímaussaq complex in Southwest Greenland are the largest known layered peralkaline intrusive complexes. Both host world-class deposits rich in REE and other high-tech elements. Both complexes expose spectacular layering with horizons rich in eudialyte group minerals (EGM). We present a detailed study of the composition and cryptic variations in cumulus EGM from Lovozero and a comparison with EGM from Ilímaussaq to further our understanding of peralkaline magma chambers processes. The geochemical signatures of Lovozero and Ilímaussaq EGM are distinct. In Lovozero EGMs are clearly enriched in Na + K, Mn, Ti, Sr and poorer Fe compared to EGM from Ilímaussaq, whereas the contents of ΣREE + Y and Cl are comparable. Ilímaussaq EGMs are depleted in Sr and Eu, which points to plagioclase fractionation and an olivine basaltic parent. The absence of negative Sr and Eu anomalies suggest a melanephelinitic parent for Lovozero. In Lovozero the cumulus EGMs shows decrease in Fe/Mn, Ti, Nb, Sr, Ba and all HREE up the magmatic layering, while REE + Y and Cl contents increase. In Lovozero EGM spectra show only a weak enrichment in LREE relative to HREE. The data demonstrates a systematic stratigraphic variation in major and trace elements compositions of liquidus EGM in the Eudialyte Complex, the latest and uppermost part of Lovozero. The distribution of elements follows a broadly linear trend. Despite intersample variations, the absence of abrupt changes in the trends suggests continuous crystallization and accumulation in the magma chamber. The crystallization was controlled by elemental distribution between EGM and coexisting melt during gravitational accumulation of crystals and/or mushes in a closed system. A different pattern is noted in the Ilimaussaq Complex. The elemental trends have variable steepness up the magmatic succession especially in the uppermost zones of the Complex. The differences between the two complexes are suggested to be related dynamics of the crystallization and accumulation processes in the magma chambers, such as arrival of new liquidus phases and redistributions by mush melts. Full article
(This article belongs to the Special Issue Study of the Eudialyte Group Minerals)
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18 pages, 3339 KiB  
Article
Chemical Composition and Petrogenetic Implications of Eudialyte-Group Mineral in the Peralkaline Lovozero Complex, Kola Peninsula, Russia
by Lia Kogarko and Troels F. D. Nielsen
Minerals 2020, 10(11), 1036; https://doi.org/10.3390/min10111036 - 20 Nov 2020
Cited by 14 | Viewed by 4575
Abstract
Lovozero complex, the world’s largest layered peralkaline intrusive complex hosts gigantic deposits of Zr-, Hf-, Nb-, LREE-, and HREE-rich Eudialyte Group of Mineral (EGM). The petrographic relations of EGM change with time and advancing crystallization up from Phase II (differentiated complex) to Phase [...] Read more.
Lovozero complex, the world’s largest layered peralkaline intrusive complex hosts gigantic deposits of Zr-, Hf-, Nb-, LREE-, and HREE-rich Eudialyte Group of Mineral (EGM). The petrographic relations of EGM change with time and advancing crystallization up from Phase II (differentiated complex) to Phase III (eudialyte complex). EGM is anhedral interstitial in all of Phase II which indicates that EGM nucleated late relative to the main rock-forming and liquidus minerals of Phase II. Saturation in remaining bulk melt with components needed for nucleation of EGM was reached after the crystallization about 85 vol. % of the intrusion. Early euhedral and idiomorphic EGM of Phase III crystalized in a large convective volume of melt together with other liquidus minerals and was affected by layering processes and formation of EGM ore. Consequently, a prerequisite for the formation of the ore deposit is saturation of the alkaline bulk magma with EGM. It follows that the potential for EGM ores in Lovozero is restricted to the parts of the complex that hosts cumulus EGM. Phase II with only anhedral and interstitial EGM is not promising for this type of ore. Nor is the neighboring Khibiny complex despite a bulk content of 531 ppm of Zr. Khibiny only has interstitial and anhedral EGM. The evolution of the Lovozero magma is recorded in the compositions EGM up through a stratigraphy of 2400 m in Phase II and III of the complex, and distinct in elements like rare earth elements (REE), Sr, Ba, Th, U, Rb, Mn, Fe. The compositional evolution reflects primarily fractional crystallization processes within the magma chamber itself in combination with convective magma flow and layering by precipitation of minerals with different settling velocities. The suggested mechanism for the formation of the EGM deposits is flotation of very small, suspended EGM crystals in the convective magma and concentration below the roof of the magma chamber. Phase III EGM is enriched in total REE (1.3%) and in HREE (Ce/Yt = 8.8) and constitutes a world class deposit of REE in the million tons of Phase III eudialyte lujavrites. Full article
(This article belongs to the Special Issue Study of the Eudialyte Group Minerals)
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14 pages, 5149 KiB  
Article
Metallogenic Epoch and Tectonic Setting of Saima Niobium Deposit in Fengcheng, Liaoning Province, NE China
by Nan Ju, Yun-Sheng Ren, Sen Zhang, Zhong-Wei Bi, Lei Shi, Di Zhang, Qing-Qing Shang, Qun Yang, Zhi-Gao Wang, Yu-Chao Gu, Qiu-Shi Sun and Tong Wu
Minerals 2019, 9(2), 80; https://doi.org/10.3390/min9020080 - 29 Jan 2019
Cited by 13 | Viewed by 4059
Abstract
The Saima deposit is a newly discovered niobium deposit which is located in the eastern of Liaoning Province, NE China. Its mineralization age and geochemical characteristics are firstly reported in this study. The Nb orebodies are hosted by the grey–brown to grass-green aegirine [...] Read more.
The Saima deposit is a newly discovered niobium deposit which is located in the eastern of Liaoning Province, NE China. Its mineralization age and geochemical characteristics are firstly reported in this study. The Nb orebodies are hosted by the grey–brown to grass-green aegirine nepheline syenite. Detailed petrographical studies show that the syenite consists of orthoclase (~50%), nepheline (~30%), biotite (~15%) and minor arfvedsonite (~3%) and aegirine (~2%), with weak hydrothermal alteration dominated by silicification. In situ LA-ICP-MS zircon U-Pb dating indicates that the aegirine nepheline syenite was emplaced in the Late Triassic (229.5 ± 2.2 Ma), which is spatially, temporally and genetically related to Nb mineralization. These aegirine nepheline syenites have SiO2 contents in the range of 55.86–63.80 wt. %, low TiO2 contents of 0.36–0.64 wt. %, P2O5 contents of 0.04–0.11 wt. % and Al2O3 contents of more than 15 wt. %. They are characterized by relatively high (K2O + Na2O) values of 9.72–15.51 wt. %, K2O/Na2O ratios of 2.42–3.64 wt. % and Rittmann indexes (σ = [ω(K2O + Na2O)]2/[ω(SiO2 − 43)]) of 6.84–17.10, belonging to the high-K peralkaline, metaluminous type. These syenites are enriched in large ion lithophile elements (LILEs, e.g., Cs, Rb and Ba) and light rare earth elements (LREEs) and relatively depleted in high field strength elements (HFSEs, e.g., Nb, Zr and Ti) and heavy rare earth elements (HREEs), with transitional elements showing an obvious W-shaped distribution pattern. Based on these geochronological and geochemical features, we propose that the ore-forming intrusion associated with the Nb mineralization was formed under post-collision continental-rift setting, which is consistent with the tectonic regime of post-collision between the North China Craton and Paleo-Asian oceanic plate during the age in Ma for Indosinian (257–205 Ma). Intensive magmatic and metallogenic events resulted from partial melting of lithospheric mantle occurred during the post-collisional rifting, resulting in the development of large-scale Cu–Mo mineralization and rare earth deposits in the eastern part of Liaoning Province. Full article
(This article belongs to the Special Issue Polymetallic Metallogenic System)
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12 pages, 1646 KiB  
Review
Rare Earth Element Deposits of Alkaline Igneous Rocks
by Jaroslav Dostal
Resources 2017, 6(3), 34; https://doi.org/10.3390/resources6030034 - 25 Jul 2017
Cited by 169 | Viewed by 26736
Abstract
Alkaline igneous complexes host deposits of rare earth elements (REE), which represent one of the most economically important resources of heavy REE and Yttrium (Y). The hosts are differentiated rocks ranging from nepheline syenites and trachytes to peralkaline granites. These complexes usually occur [...] Read more.
Alkaline igneous complexes host deposits of rare earth elements (REE), which represent one of the most economically important resources of heavy REE and Yttrium (Y). The hosts are differentiated rocks ranging from nepheline syenites and trachytes to peralkaline granites. These complexes usually occur in continental within-plate tectonic settings associated with rifts, faults, or hotspot magmatism. The REE mineralization is found in layered alkaline complexes, granitic stocks, and late-stages dikes and rarely trachytic volcanic and volcaniclastic deposits. The bulk of REE is present in accessory minerals, which can reach percentage levels in mineralized zones. The mineralization contains various REE-bearing minerals that can display complex replacement textures. Main REE minerals present in these deposits are bastnäsite, eudialyte, loparite, gittinsite, xenotime, monazite, zircon, and fergusonite. The parent magmas of alkaline igneous complexes are derived from partial melts of mantle sources. Protracted fractional crystallization of the magma led to an enrichment in REE, particularly in the late stages of magma evolution. The primary magmatic mineralization is commonly overprinted (remobilized and enriched) by late magmatic to hydrothermal fluids. Elevated abundances of U and Th in the deposits make a gamma-ray (radiometric) survey an important exploration tool, but also represent a significant environmental challenge for exploitation. Full article
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