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The Sheahan Diamond Literature Reference Compilation - Technical Articles based on Major Region - Kola Peninsula
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcements called the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Region Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In addition most references have been tagged with one or more region words. In an effort to make it easier for users to track down articles related to a specific region, KRO has extracted these region words and developed a list of major region words presented in the Major Region Index to which individual region words used in the article reference have been assigned. Each individual Region Report contains in chronological order all the references with a region word associated with the Major Region word. Depending on the total for each reference type - technical, media and corporate - the references will be either in their own technical, media or corporate Region Report, or combined in a single report. Where there is a significant number of technical references there will be a technical report dedicated to the technical articles while the media and corporate references are combined in a separate region report. References that were added in the most recent monthly update are highlighted in yellow within the Region Report. The Major Region words have been defined by a scale system of "general", "continent", "country", "state or province" and "regional". Major Region words at the smaller scales have been created only when there are enough references to make isolating them worthwhile. References not tagged with a Region are excluded, and articles with a region word not matched with a Major Region show up in the "Unknown" report.
Kimberlite - diamondiferous
Lamproite - diamondiferous
Lamprophyre - diamondiferous
Other - diamondiferous
Kimberlite - non diamondiferous
Lamproite - non diamondiferous
Lamprophyre - non diamondiferous
Other - non diamondiferous
Kimberlite - unknown
Lamproite - unknown
Lamprophyre - unknown
Other - unknown
Future Mine
Current Mine
Former Mine
Click on icon for details about each occurrence. Works best with Google Chrome.
CITATION: Faure, S, 2010, World Kimberlites CONSOREM Database (Version 3), Consortium de Recherche en Exploration Minérale CONSOREM, Université du Québec à Montréal, Numerical Database on consorem.ca. NOTE: This publicly available database results of a compilation of other public databases, scientific and governmental publications and maps, and various data from exploration companies reports or Web sites, If you notice errors, have additional kimberlite localizations that should be included in this database, or have any comments and suggestions, please contact the author specifying the ID of the kimberlite: [email protected]
General Petrological Aspects of Paleozoic Alkali Magmatism In the Kola Peninsula and the Rare Earth Distribution in Alkali Ultrabasic Lamprophyre Dikes.
Geochemistry International (Geokhimiya), Vol. 15, No. 3, PP. 124-135.
Arzamastsev, A.A., Bea, F., Arzamastseva, L.V., Montero, P.
Devonian plume magmatism in the NE Baltic Shield: rare earth elements in rocks and minerals of ultrabasic alkaline series as indicators of magma evolution.
Deep Seated Magmatism, magmatism sources and the problem of plumes., pp. 42-68.
Magmatic evolution of the differentiated ultramafic, alkaline and carbonatite intrusion of Vuoriyarvi, Kola Peninsula, Russia, A LA ICP MS study of apatite.
Geochemistry and mineralogy of HFSE in intracratonic carbonatites: implications for their economic potential (on the example of Kola alkaline province).
GAC Annual Meeting Halifax May 15-19, Abstract 1p.
Kovdor apatite francolite deposit as an example of explosive and phreatomagmatic endogeneous activity in the ultramafic alkaline and carbonatite complex Kola.
Plumes and problems of deep sources of alkaline magmatism, pp. 155-170.
Noble gas isotopes in minerals from phoscorites and carbonatites in Kovdor and Seblyavr ultramafic alkaline complexes ( Kola alkaline province NW Russia).
Periodico di Mineralogia, (in english), Vol. LXX11, 1. April, pp. 135-146.
Sr Na REE titanates of the crichtonite group from a fenitized megaxenolith, Khibin a alkaline complex, Kola Peninsula, Russia: first occurrence and implications.
European Journal of Mineralogy, Vol. 18, 4, August pp. 493-502.
Magmatic evolution of the differentiated ultramafic, alkaline and carbonatite intrusion of Vuoriyarvi ( Kola Peninsula) Russia, A LA-ICP-MS study of apatite.
Mertanen, S., Vuollo, J.I., Huhma, H., Arestova, N.A., Kovalenko, A.
Early Paleoproterozoic Archean dykes and gneisses in Russian Karelia of the Fennoscandian Shield - new paleomagnetic, isotope age, geochemical investigations.
Precambrian Research, Vol. 144, 3-4, Feb. 10, pp. 239-260.
Tichomirowa, M., Grosche, G., Gotze, J., Belyatsky, B.V., Savva, E.V., Keller, J., Todt, W.
The mineral isotope composition of two Precambrian carbonatite complexes from the Kola Alkaline Province - alteration versus primary magmatic signatures.
Janik, T., Kozlovskaya, E., Helikkinen, P., Tliniemi, J.
Evidence for preservation of crustal root beneath the Proterozoic Lapland-Kola orogen ( northern Fennoscandian shield) derived from P and S wave models.
Journal of Geophysical Research, Vol. 114. B 6, B06308.
Plume related mantle source of super large rare metal deposits from the Lovozero and Khibin a massifs on the Kola Peninsula, east Baltic Shield: Sr, Nd, Hf isotope ssytematics.
Lehtonen, M., O'Brien, H., Peltonen, P., Kukkonen, I., Ustinov, V., Verzhak, V.
Mantle xenocrysts from the Arkangelskaya kimberlite (Lomonosov); constraints on the composition and thermal state of the Diamondiferous lithospheric mantle.
Apparent partial loss 40Ar 39 Ar age spectra of hornblende from the Paleoproterozic Lapland Kola orogen ( Arctic European Russia): insights into modelling ....
Geosciences Journal, Vol. 13, 3, Sept. pp. 317-329.
Zozulya, D.R., O'Brien, H., Peltonen, P., Lehtonen, M.
Thermobarometry of mantle derived garnets and pyroxenes of Kola region ( NW Russia): lithosphere composition, thermal regime and diamond prospectivity.
Bulletin of the Geological Society of Finland, Vol. 81, pp. 143-158.
Zozulya, D.R., O'Brien, H., Peltonen, P., Lehtonen, M.
Thermobarometry of mantle derived garnets and pyroxenes of Kola region ( NW Russia): lithosphere composition, thermal regime and diamond prospectivity.
Bulletin of the Geological Society of Finland, Vol. 81, pp. 143-158.
The alkaline ultrabasic magmatism of the Onega peninsula Nenoksa fields - reflection (display) of the plume and subduction processes in Belomorsky region.
Vladykin, N.V., Deep Seated Magmatism: its sources and plumes, pp. 145-163.
Crystal chemistry of natural layered double hydroxides from the Kovdor alkaline massif, Kola. Polytypes of quininite: cation ordering and superstructures.
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Comparative in-situ U-Th-Pb geochronology and trace element composition of baddeleyite and low U zircon from carbonatites of the Paleozoic Kovdor, Kola Pen.
Kazanskyite, Ba Ti Nb Na3 Ti (Si207) 202 (OH) 2 (H20)4, a group III Ti disilicate mineral from the Khibiny alkaline massif, Kola Peninsula, Russia: description and crystal structure.
Comparative in-situ U-Th-Pb geochronology and trace element composition of baddeleyite and low U-zircon from carbonatites of the Paleozoic Kovdor alkaline ultramafic complex Kola Peninsula, Russia.
Tichomirowa, M., Whitehouse, M., Gerdes, A., Gotze, J.
Carbonatite metasomatism: evidence from geochemistry and isotope composition ( U-Pb, Hf, O) on zircons from two Precambrian carbonatites of the Kola alkaline province.
Tretyachenko, W., Bovkun, A.V., Garanin, K.V., Garanin, V.K., Tretyachenko, N.G.
Formation features of the early Hercynic alkaline ultrabasic and basic volcanic complexes from Zimny Bereg area, north east of Archangelsk region, Russia.
10th. International Kimberlite Conference Held Bangalore India Feb. 6-11, Poster abstract
Evolution of deep crustal roots of the Arhangelsk Diamondiferous province: evidences from crustal xenoliths and xenocrysts from Devonian kimberlite pipes.
Conodonts in xenoliths from kimberlite pipes of the southeastern White Sea region ( Arkhangelsk Oblast): key to Ordovician stratigraphic and paleogeographic reconstructions of the East European Platform.
Camara, F., Skolova, E., Abdu, Y.A., Hawthorne, F.C.
Nafertisite Na3Fe2 10Ti2(Si6017)02(OH)6F(H2))2 from Mt. Kukisvumchorr Khibiny alkaline massif, Kola Peninsula, Russia: refinement of the crystal structure and revision of the chemical formula.
European Journal of Mineralogy, Vol. 26, pp. 689-700.
Zircon trace element characteristics and ages in granulite xenoliths: a key to understanding the age and origin of the lower crust, Arkhangelsk kimberlite province, Russia.
Contributions to Mineralogy and Petrology, Vol. 167, pp. 973-980.
Korikovsky, S., Kotov, A., Salnikova, E., Aranovich, L., Korpechkov, D., Yakovleva, S., Tolmacheva, E., Anisimova, I.
The age of the protolith of metamorphic rocks in the southeastern Lapland granulite belt, southern Kola Peninsula: correlation with the Belomorian mobile belt in the context of the problem of Archean eclogites.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Post collisional lamproites of the Por'ya Guba dike fields.
East European Craton: Early Precambrian history & 3 D. Model Authors: M.V. Mints, K.A. Dokukina, A.N. Konilov, I.B. Philippova, C.L. Zlobin., GSA SPE 510, 433p. Chapter 11, section 3
Equigranualr eclogites from the V. Grib kimberlite pipe: evidence for Paleoproterozoic subduction on the territory of the Arkangelsk Diamondiferous province.
Abstract: The petrochemistry of carbonatites of three formation types were studied: (1) ultrahigh-pressure garnet-containing carbonatites (UHPC) of the Caledonian sheet (Tromsö, Norway); (2) rocks of the carbonatite-lkaline-ultrabasic Kovdor massif (the Kola Peninsula); and (3) rocks of the carbonatite-alkaline-gabbroid Tikshozero massif (north of Karelia). The samples of carbonatites were examined and tested with a microprobe; the microelements were determined using the ICP-MS technique at the Institute of Microelectronics Technology and High Purity Materials (Chernogolovka). The carbonatites of the Kovdor and Tikshozero massifs are characterized by similar negative REE trends, with a degree of REE enrichment of the Tikshozero carbonatites. The UHPC from Tromsö are different from those of the Kovdor and Tikshozero massifs in the negative trend along with lower concentrations of light REEs. The Tromsö UHPC are similar to the carbonatites of the Kovdor and Tikshozero massifs in the trend and concentrations of heavy REEs. The carbonatites of the Fennoscandian shield of various formation times and types are characterized by the geochemical similarity to those in different regions of the world with the sources associated to mantle plumes. This similarity might be caused by the formation of the mantle carbonated magmas of carbonatite-containing igneous complexes from a mantle source enriched under either mantle metasomatism or plume-lithosphere interaction, with similar mechanisms of formation. The appearance of the formations as such within a wide time interval points to the long-term occurrence of a superplume at the Fennoscandian shield and to permanent activation of the related processes of magma formation.
Abstract: The occurrence, morphology, and composition of rinkite are considered against the background of zoning in the Khibiny pluton. Accessory rinkite is mostly characteristic of foyaite in the outer part of pluton, occurs somewhat less frequently in foyaite and rischorrite in the central part of pluton, even more sparsely in foidolites and apatite-nepheline rocks, and sporadically in fenitized xenoliths of the Lovozero Formation. The largest, up to economic, accumulations of rinkite are related to the pegmatite and hydrothermal veins, which occur in nepheline syenite on both sides of the Main foidolite ring. The composition of rinkite varies throughout the pluton. The Ca, Na, and F contents in accessory rinkite and amorphous products of its alteration progressively increase from foyaite and fenitized basalt of the Lovozero Formation to foidolite, rischorrite, apatite-nepheline rocks, and pegmatite-hydrothermal veins.
Abstract: Zirconolite, its Ce-, Nd-, and Y-analogs, and laachite, another member of the zirconolite group, are typomorphic minerals of the fenitized xenoliths in nepheline syenite and foidolite of the Khibiny-Lovozero Complex, Kola Peninsula, Russia. All these minerals are formed at the late stage of fenitization as products of ilmentie alteration under the effect of Zr-bearing fluids. The diversity of these minerals is caused by the chemical substitutions of Na and Ca for REE, Th, and U compensated by substitution of Ti and Zr for Nb, Fe and Ta, as well as by the redistribution of REE between varieties enriched in Ti (HREE) or Nb (LREE). The results obtained can be used in the synthesis of Synroc-type titanate ceramics assigned for the immobilization of actinides.
Abstract: The crystal structure of betalomonosovite, ideally Na6?4Ti4(Si2O7)2[PO3(OH)][PO2(OH)2]O2(OF), a 5.3331(7), b 14.172(2), c 14.509(2) Å, ? 103.174(2), ? 96.320(2), ? 90.278(2)°, V 1060.7(4) Å3, from the Lovozero alkaline massif, Kola peninsula, Russia, has been refined in the space group PFormula to R = 6.64% using 3379 observed (Fo > 4?F) reflections collected with a single-crystal APEX II ULTRA three-circle diffractometer with a rotating-anode generator (MoK?), multilayer optics, and an APEX-II 4K CCD detector. Electron-microprobe analysis gave the empirical formula (Na5.39Ca0.36Mn0.04Mg0.01)?5.80 (Ti2.77Nb0.48Mg0.29Fe3+0.23Mn0.20Zr0.02Ta0.01)?4(Si2.06O7)2[P1.98O5(OH)3]O2[O0.82F0.65(OH)0.53]?2, Dcalc. = 2.969 g cm?3, Z = 2, calculated on the basis of 26 (O + F) apfu, with H2O determined from structure refinement. The crystal structure of betalomonosovite is characterized by extensive cation and anion disorder: more than 50% of cation sites are partly occupied. The crystal structure of betalomonosovite is a combination of a titanium silicate (TS) block and an intermediate (I) block. The TS block consists of HOH sheets (H-heteropolyhedral, O-octahedral) and exhibits linkage and stereochemistry typical for Group IV (Ti + Mg + Mn = 4 apfu) of the TS-block minerals. The I block is a framework of Na polyhedra and P tetrahedra which ideally gives {Na2?4[PO3(OH)][PO2(OH)2]} pfu. Betalomonosovite is an Na-poor OH-bearing analogue of lomonosovite, Na10Ti4(Si2O7)2(PO4)2O4. In the betalomonosovite structure, there is less Na in the I block and in the TS block when compared to the lomonosovite structure. The OH groups occur mainly in the I block where they coordinate P and Na atoms and in the O sheet of the TS block (minor). The presence of OH groups in the I block and in the TS block is supported by IR spectroscopy and bond-valence calculations on anions. High-resolution TEM of lomonosovite shows the presence of pervasive microstructural intergrowths, accounting for the presence of signals from H2O in the infrared spectrum of anhydrous lomonosovite. More extensive lamellae in betalomonosovite suggest a topotactic reaction from lomonosovite to betalomonosovite.
Abstract: Fe-rich carbonatites with a mineral assemblage of ankerite-calcite or siderite are widespread in southern Siberia, Russia. The siderite carbonatites are associated with F-Ba-Sr-REE mineralization and have a 40Ar/39Ar age of 117.2 ± 1.3 Ma. Melt and fluid inclusions suggest that the carbonatites formed from volatile-rich alkali- and chloride-bearing carbonate melts. Ankerite-calcite carbonatites formed from carbonatite melt at a temperature of more than 790 °C. The ferrocarbonatites (the second phase of carbonatite intrusion) formed from a sulfate-carbonate-chloride fluid phase (brine-melt) at >650 °C and ?360 MPa. The brine-melt fluid phase had high concentrations of Fe and LREEs. A subsequent hydrothermal overprint contributed to the formation of economically important barite-Sr-fluorite-REE mineralization in polymict siderite breccia.
Mineralogical Society Series, isbn 0-903056-22-4 on sale approx 20lbs
Russia, Kola Peninsula
Book - volcanology
Abstract: The first response to the title of this book is often 'What is a phoscorite?'. The exact definition and characteristics of phoscorite are discussed in some detail in Chapter 2 and were the subject of varying opinions amongst the authors of this and other chapters. We nicknamed the book 'the dark side of carbonatites', which covers it nicely. Phoscorites are dark, often very handsome, sometimes economically valuable, magnetite-apatite-silicate rocks, almost always associated with carbonatite. They are key to understanding the longstanding question of how carbonate and carbonate-bearing magmas rise to the crust and the Earth's surface. Despite this, they have been given little attention; a search on geological literature databases will produce thousands of references to carbonatite (up to 4125 on Georef) but not more than thirty references to phoscorite. This book goes some way to redress this balance. Over the last ten years many European and North American scientists have studied Kola rocks in collaboration with Russian colleagues. The idea for this book came from one such project funded by the European organisation, INTAS (Grant No 97-0722). The Kola Peninsula, Russia, is one of the outstanding areas in the World for the concentration and economic importance of alkaline rocks. However, Russian work on the Kola complexes is still relatively
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Journal of Volcanology and Seismology, Vol. 10, 5, pp. 339-346.
Russia, Kola Peninsula, Archangel
Deposit- Lomonsov
Abstract: This paper presents results from a study of the Lomonosov volcanic pipe as derived from anomalies of the microseismic field. Microseismic sounding revealed that this volcanic pipe is a cone-shaped body with a small gradient of microseismic intensity motion (2 to 5 dB). Discontinuities generally show greater contrasts compared with the variations of microseismic motion in the pipe body. Comparison of the results of this microseismic sounding with other geological and geophysical data showed that the intensities of the micro-seismic field along lines that traversed the pipe reflect realistic structures of a kimberlite pipe and the host rocks. The method of microseismic sounding was used to reconstruct the deeper structure of the volcanic pipe and the host rocks down to depths greater than 2 km. We estimated the velocity contrast and the errors involved in the identification of vertical boundaries of the pipe. The volcanic pipe has a shape that is consistent with a nearly vertical source situated at a depth of a few hundred meters. This is hypothesized to be a typical occurrence for other diamond-bearing pipes as well.
Abstract: The paper reports detailed data on phlogopite from kimberlite of three facies types in the Arkhangelsk Diamondiferous Province (ADP): (i) massive magmatic kimberlite (Ermakovskaya-7 Pipe), (ii) transitional type between massive volcaniclastic and magmatic kimberlite (Grib Pipe), and (iii) volcanic kimberlite (Karpinskii-1 and Karpinskii-2 pipes). Kimberlite from the Ermakovskaya-7 Pipe contains only groundmass phlogopite. Kimberlite from the Grib Pipe contains a number of phlogopite populations: megacrysts, macrocrysts, matrix phlogopite, and this mineral in xenoliths. Phlogopite macrocrysts and matrix phlogopite define a single compositional trend reflecting the evolution of the kimberlite melt. The composition points of phlogopite from the xenoliths lie on a single crystallization trend, i.e., the mineral also crystallized from kimberlite melt, which likely actively metasomatized the host rocks from which the xenoliths were captured. Phlogopite from volcaniclastic kimberlite from the Karpinskii-1 and Karpinskii-2 pipes does not show either any clearly distinct petrographic setting or compositional differentiation. The kimberlite was dated by the Rb-Sr technique on phlogopite and additionally by the 40Ar/39Ar method. Because it is highly probable that phlogopite from all pipes crystallized from kimberlite melt, the crystallization age of the kimberlite can be defined as 376 ± 3 Ma for the Grib Pipe, 380 ± 2 Ma for the Karpinskii-1 pipe, 375 ± 2 Ma for the Karpinskii-2 Pipe, and 377 ± 0.4 Ma for the Ermakovskaya-7 Pipe. The age of the pipes coincides within the error and suggests that the melts of the pipes were emplaced almost simultaneously. Our geochronologic data on kimberlite emplacement in ADP lie within the range of 380 ± 2 to 375 ± Ma and coincide with most age values for Devonian alkaline-ultramafic complexes in the Kola Province: 379 ± 5 Ma; Arzamastsev and Wu, 2014). These data indicate that the kimberlite was formed during the early evolution of the Kola Province, when alkaline-ultramafic complexes (including those with carbonatite) were emplaced.
Abstract: This paper presents new major and trace element data from 150 garnet xenocrysts from the V. Grib kimberlite pipe located in the central part of the Arkhangelsk diamondiferous province (ADP). Based on the concentrations of Cr2O3, CaO, TiO2 and rare earth elements (REE) the garnets were divided into seven groups: (1) lherzolitic “depleted” garnets (“Lz 1”), (2) lherzolitic garnets with normal REE patterns (“Lz 2”), (3) lherzolitic garnets with weakly sinusoidal REE patterns (“Lz 3”), (4) lherzolitic garnets with strongly sinusoidal REE patterns (“Lz 4”), (5) harzburgitic garnets with sinusoidal REE patterns (“Hz”), (6) wehrlitic garnets with weakly sinusoidal REE patterns (“W”), (7) garnets of megacryst paragenesis with normal REE patterns (“Meg”). Detailed mineralogical and geochemical garnet studies and modeling results suggest several stages of mantle metasomatism influenced by carbonatite and silicate melts. Carbonatitic metasomatism at the first stage resulted in refertilization of the lithospheric mantle, which is evidenced by a nearly vertical CaO-Cr2O3 trend from harzburgitic (“Hz”) to lherzolitic (“Lz 4”) garnet composition. Harzburgitic garnets (“Hz”) have probably been formed by interactions between carbonatite melts and exsolved garnets in high-degree melt extraction residues. At the second stage of metasomatism, garnets with weakly sinusoidal REE patterns (“Lz 3”, “W”) were affected by a silicate melt possessing a REE composition similar to that of ADP alkaline mica-poor picrites. At the last stage, the garnets interacted with basaltic melts, which resulted in the decrease CaO-Cr2O3 trend of “Lz 2” garnet composition. Cr-poor garnets of megacryst paragenesis (“Meg”) could crystallize directly from the silicate melt which has a REE composition close to that of ADP alkaline mica-poor picrites. P-T estimates of the garnet xenocrysts indicate that the interval of ?60-110 km of the lithospheric mantle beneath the V. Grib pipe was predominantly affected by the silicate melts, whereas the lithospheric mantle deeper than 150 km was influenced by the carbonatite melts.
Abstract: This paper focuses on the occurrences of tholeiitic magmatism in the northeastern Fennoscandian shield. It was found that numerous dolerite dikes of the Pechenga, Barents Sea, and Eastern Kola swarms were formed 380-390 Ma ago, i.e., directly before the main stage of the Paleozoic alkaline magmatism of the Kola province. The isotope geochemical characteristics of the dolerites suggest that their primary melts were derived from the mantle under the conditions of the spinel lherzolite facies. The depleted mantle material from which the tholeiites were derived shows no evidence for metasomatism and enrichment in high fieldstrength and rare earth elements, whereas melanephelinite melts postdating the tholeiites were generated in an enriched source. It was shown that the relatively short stage of mantle metasomatism directly after the emplacement of tholeiitic magmas was accompanied by significant mantle fertilization. In contrast to other large igneous provinces, where pulsed intrusion of large volumes of tholeiitic magmas coinciding or alternating with phases of alkaline magmatism was documented, the Kola province is characterized by systematic evolution of the Paleozoic plume-lithosphere process with monotonous deepening of the level of magma generation, development of mantle metasomatism and accompanying fertilization of mantle materials, and systematic changes in the composition of melts reaching the surface.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 220 Abstract
Russia, Archangel, Kola Peninsula
Deposit - Grib
Abstract: Kimberlite is a composite rock that contains juvenile magmatic material and xenoliths of crustal and mantle rocks, including metasomatically reworked rocks and megacrysts. In spite of nearly 40-50 years of continuous study of kimberlites and SCLM, some aspects of their origin remain controversial. In particular, it is unclear yet whether the megacrysts are magmatic or metasomatic in origin and how they are related to kimberlite magmas. In this contribution, we compare the major (EMPA) and trace element (SIMS, LA-ICP-MS) compositions of clinopyroxene megacrysts from the Grib kimberlite (Arkhangelsk province, Russia) with clinopyroxenes from metasomatic clinopyroxene-phlogopite xenoliths and garnet peridotite xenoliths. The Grib kimberlite (376±3 Ma, Larionova et al., 2016) is located in the central part of the Arkhangelsk province (the northern part of the East European craton) in the Chernoozero kimberlite field. The geochemical composition of the kimberlites is similar to widespread South Africa group I kimberlites . The Grib kimberlite is well known for hosting a variety of mantle xenoliths, e.g., garnet peridotite, sheared peridotite, eclogite, metasomatised mantle material, as well as megacrysts of clinopyroxene, garnet, olivine, phlogopite, and ilmenite. The clinopyroxene megacrysts occur as rounded or angular grains up to 2 cm in size. They are usually surrounded by ultrafine kimberlite rim. The xenoliths of the metasomatic clinopyroxene-phlogopite rocks reach up to 6 cm in size and have a granoblastic texture. They consist of clinopyroxene (55 vol. %), phlogopite (45 vol. %) and minor calcite, barite, perovskite. Some clinopyroxene grains contain inclusion of relict olivine that is similar in composition to olivine from mantle-derived peridotite xenoliths within the Grib kimberlite (Sazonova et al., 2015). This suggests that these xenoliths could be formed by metasomatic reworking of SCLM peridotites. The megacryst clinopyroxene is compositionally similar to the clinopyroxene found in metasomatic xenoliths and corresponds to diopside. As compared to the typical clinopyroxene megacrysts worldwide, it has higher Mg# (>0.92), Cr# (0.21-0.62) and Ca# values (0.47-0.49) and lower Ti (659-1966 ppm) composition. The clinopyroxenes have (La/Sm)CI values from 0.58 to 1.57, and trace element patterns with deep negative Ti and shallow negative Zr-Hf anomalies. The major and trace-element compositions of these clinopyroxenes are very close to those of clinopyroxenes from garnet peridotite xenoliths in the Grib pipe (Kargin et al., 2016) that could be formed during the ascent and interaction of kimberlite mamas with a surrounding lithospheric mantle after crystallization of garnet and ilmenite megacrysts. Calculations showed that metasomatic agents in equilibrium with clinopyroxene megacrysts are similar in composition to kimberlite, which is consistent with proposed model. To sum up, we suggest that the formation of clinopyroxenes of megacrysts and mantle-derived clinopyroxene-phlogopite metasomatic xenoliths from the Grib kimberlite was related to the late-stage metasomatic reworking of SCLM by kimberlite magmas.
Abstract: A quartzolite from the Rova occurrence, Keivy alkali granite province, Kola Peninsula, Russia, is used to examine the differing responses of certain rare-metal minerals during interaction with hydrothermal fluids. The minerals are two silicates [chevkinite-(Ce) and zircon], a phosphate [monazite-(Ce)] and an oxide [fergusonite-(Y)]. Textural evidence is taken to show that the dominant alteration mechanism was interface-coupled dissolution-reprecipitation. Zircon was the most pervasively altered, possibly by broadening of cleavage planes or fractures; the other minerals were altered mainly on their rims and along cracks. The importance of cracks in promoting fluid access is stressed. The compositional effects of the alteration of each phase are documented. The hydrothermal fluids carried few ligands capable of transporting significant amounts of rare-earth elements (REE), high field strength elements (HFSE) and actinides; alteration is inferred to have been promoted by mildly alkaline, Ca-bearing fluids. Expansion cracks emanating from fergusonite-(Y) are filled with unidentified material containing up to 35 wt% UO2 and 25 wt% REE2O3, indicating late-stage, short-distance mobility of these elements. Electron microprobe chemical dating of monazite yielded an age of 1665 ± 22 Ma, much younger than the formation age of the Keivy province (2.65-2.67 Ga) but comparable to that of the Svecofennian metamorphic event which affected the area (1.9-1.7 Ga) or during fluid-thermal activation of the region during rapakivi granite magmatism (1.66-1.56 Ga). Dates for altered monazite range from 2592 ± 244 Ma to 773 ± 88 Ma and reflect disturbance of the U-Th-Pb system during alteration.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92-0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05-0.23), Zr/Nb (0.28-0.80), and Zn/Cu (3-20) ratios and low Li concentrations (1.2-2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90-0.93, high Ti concentrations (100-300 ppm), high ratios Ti/Na (0.90-2.39), Zr/Nb (0.31-1.96), and Zn/Cu (12-56), elevated Li concentrations (1.9-3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water-silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Contributions to Mineralogy and Petrology, Vol. 172, 32p.
Russia, Kola Peninsula
Carbonatite
Abstract: The Lovozero alkaline massif—an agpaitic nepheline syenite layered intrusion—is located in the central part of the Kola Peninsula, Russia, and belongs to the Kola ultramafic alkaline and carbonatitic province (KACP) of Devonian age. Associated loparite and eudialyte deposits, which contain immense resources of REE, Nb, Ta, and Zr, constitute a world class mineral district. Previous Sr, Nd, and Hf isotope investigations demonstrated that these rocks and mineral deposits were derived from a depleted mantle source. However, because the Sr, Nd, and Hf abundances in the Kola alkaline rocks are significantly elevated, their isotopic compositions were relatively insensitive to contamination by the underlying crustal rocks through which the intruding magmas passed. Pb occurring in relatively lower abundance in the KACP rocks, by contrast, would have been a more sensitive indicator of an acquired crustal component. Here, we investigate the lead isotopic signature of representative types of Lovozero rocks in order to further characterize their sources. The measured Pb isotopic composition was corrected using the determined U and Th concentrations to the age of the crystallization of the intrusion (376?±?28 Ma, based on a 206Pb/204Pb versus 238U/204Pb isochron and 373?±?9 Ma, from a 208Pb/204Pb versus 232Th/204Pb isochron). Unlike the previously investigated Sr, Nd, and Hf isotopes, the lead isotopic composition plot was well outside the FOZO field. The 206Pb/204Pb values fall within the depleted MORB field, with some rocks having lower 207Pb/204Pb but higher 208Pb/204Pb values. Together with other related carbonatites having both lower and higher 206Pb/204Pb values, the combined KACP rocks form an extended linear array defining either a?~2.5-Ga secondary isochron or a mixing line. The projection of this isotopic array toward the very unradiogenic composition of underlying 2.4-2.5-Ga basaltic rocks of the Matachewan superplume and associated Archean granulite facies country rock provides strong evidence that this old lower crust was the contaminant responsible for the deviation of the Lovozero rocks from a presumed original FOZO lead isotopic composition. Evaluating the presence of such a lower crustal component in the Lovozero rock samples suggests a 5-10% contamination by such rocks. Contamination by upper crustal rock is limited to only a negligible amount.
Russia, Kola Peninsula, Europe, Finland, Canada, British Columbia
deposit - Khibina, Fir, Siilinjarvi
Abstract: Phosphorus is the central ingredient in fertilizer that allows modern agriculture to feed the world’s population. This element, also critical in a host of industrial applications, is a nonrenewable resource that is sourced primarily from the phosphatic mineral apatite, hosted in sedimentary and igneous ores. World phosphate resources are estimated by the U.S. Geological Survey at ca. 300,000 Mt, of which 95% are sedimentary and 5% are igneous. Current known USGS reserve estimates are sufficient for a maximum of 200 to 300 years; the exploration and discovery of new resources, enhanced mining technologies, and new technologies aimed at the recovery and recycling of P from sewage and agricultural runoff will all contribute to extending P production. Igneous ores are generally associated with Phanerozoic carbonatites and silica-deficient alkalic intrusions that typically average 5 to 15 wt % P2O5, which can be beneficiated to high-grade concentrates of at least 30 wt % P2O5 with few contaminants. Carbonatites are typically the smallest and youngest parts of a carbonatite-alkaline rock complex that formed during fractional crystallization of a calcic parental alkaline silicate melt, or from liquid immiscibility of a carbonate-rich nephelinite that underwent magmatic fractionation and differentiation during ascent from the mantle source. Fluorapatite generally crystallizes early, near the liquidus, and over a small temperature interval below the apatite saturation temperature that varies strongly with temperature, SiO2 and CaO concentrations, and the aluminosity of the melt. Carbonatite-alkaline rock complexes commonly possess a concentric, zonal structure thought to reflect caldera volcanism. Pathfinder elements in soils, sediments, tills, and vegetation include Nb, rare earth elements (REEs), P, Ba, Sr, F, U, and Th, and in water, F, Th, and U are indicators. Remote sensing techniques with the ability to identify minerals rich in CO3, REEs, and Fe2+ that are characteristic of carbonatites are also important exploration tools that may provide vectors to ore. Sedimentary phosphorite is a marine bioelemental sedimentary rock that contains >18 wt % P2O5. While small peritidal phosphorites formed in Precambrian coastal environments, economically significant upwelling-related phosphorite did not accumulate until the late Neoproterozoic and continued through the Phanerozoic. Coastal upwelling delivered deep, P-rich waters to continental shelves and in epeiric seas to drive phosphogenesis and form the largest phosphorites on Earth. High-grade deposits formed as a result of hydraulic concentration of phosphate grains to form granular beds with minimal gangue. The amalgamation of these beds into decameter-thick, stratiform ore zones is generally focused along the maximum flooding surface, which is a primary exploration target in upwelling-related phosphorite. In addition to P, other elements concentrated in igneous and sedimentary phosphorites are Se, Mo, Zn, Cu, and Cr, which are important agricultural micronutrients. Other saleable by-products include U and REEs. The U concentration in sedimentary phosphorite is generally between 50 and 200 ppm, but can be as high as 3,000 ppm, making it an increasingly important source of U for the nuclear industry. The concentration of REEs in some sedimentary phosphorites is comparable to the world’s richest igneous and Chinese clay-type REE deposits. The source of the dissolved P in upwelling ocean water is ultimately derived from the chemical weathering of continental rocks, the process that links igneous and sedimentary phosphorites through time and space. The covarying temporal relationship of igneous and sedimentary deposits suggests that plate tectonics and the concentration of apatite in a progressively more felsic crust underpins the feedback processes regulating the biogeochemical cycling of P. Critical to the generation of greenfield exploration targets is the recognition that large P deposits emerged in the late Neoproterozoic. The geological environments conducive for exploration can be constrained from an understanding of ore-forming processes by the use of complementary petrological techniques, including fieldwork, petrography, sedimentology, sequence stratigraphy, and geochemistry.
Neues Jahrbuch fur Mineralogie, Vol. 194, 2, pp. 165-173.
Russia, Kola Peninsula
deposit - Kovdor
Abstract: Isolueshite, a cubic complex oxide with the formula NaNbO3, occurs as euhedral crystals 0.4 - 0.7 mm in size in calcite carbonatite, Kovdor ultrabasic-alkaline complex (Kola, Russia). Average composition of isolueshite, based on 40 analyses by wavelength-dispersive electron microprobe is (Na0.84Ca0.07Sr0.01La0.01Ce0.01)?0.95(Nb0.90Ti0.11)?1.01O3. Minor and trace elements are Ti (4.1- 6.8 wt.% TiO2), REEs (1.8 - 4.0 wt.% REE2O3), Ca (1.7- 3.3 wt.% CaO), Zr (0.1- 0.8 wt.% ZrO2), Sr (0.3 - 0.4 wt.% SrO), Th (0.1- 0.5 wt.% ThO2), Fe (0.1- 0.2 wt.% Fe2O3) and Ta (0.1 wt.% Ta2O5). The crystal structure of isolueshite was refined to an agreement index (R1) of 0.028 for 82 unique reflections with |F0| ? 4 ?(F). The mineral is cubic, Pm3-m, a = 3.9045(5) Å and V = 59.525(13) Å3. The diffraction pattern of the crystal contains only regular and strong Bragg reflections with no signs of diffuse scattering. There are two sites in the crystal structure: A is 12-coordinated (A-O = 2.556(3) Å) and located at the corners of the cubic primitive cell and B is situated in the center of the unit-cell and has an octahedral coordination. The crystal-chemical formula based on the structure refinement is (Na0.84(1)Ca0.16(1))(Nb0.88(1)Ti0.12(1))O3. We suggest that isolueshite is a quenched (kinetically favored) polymorph of lueshite that formed as a result of rapid crystallization due to the sudden drop in temperature and/or pressure.
Abstract: The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92–0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05–0.23), Zr/Nb (0.28–0.80), and Zn/Cu (3–20) ratios and low Li concentrations (1.2–2.0 ppm), and the oxygen isotopic composition of this olivine ?18O = 5.64‰ is higher than that of olivine in mantle peridotites (?18O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90–0.93, high Ti concentrations (100–300 ppm), high ratios Ti/Na (0.90–2.39), Zr/Nb (0.31–1.96), and Zn/Cu (12–56), elevated Li concentrations (1.9–3.4 ppm), and oxygen isotopic composition ?18O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the ?18O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose ?18O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water–silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.
Abstract: The paper discusses questions related to the generation of increasing crustal horizontal compressive stresses compared to the idea of the standard gravitational state at the elastic stage or even from the prevalence of horizontal compression over vertical stress equal to the lithostatic pressure. We consider a variant of superfluous horizontal compression related to internal lithospheric processes occurrin in the crust of orogens, shields, and plates. The vertical ascending movements caused by these motions at the sole of the crust or the lithosphere pertain to these and the concomitant exogenic processes giving rise to denudation and, in particular, to erosion of the surfaces of forming rises. The residual stresses of the gravitational stressed state at the upper crust of the Kola Peninsula have been estimated for the first time. These calculations are based on the volume of sediments that have been deposited in Arctic seas beginning from the Mesozoic. The data speak to the possible level of residual horizontal compressive stresses up to 90 MPa in near-surface crustal units. This estimate is consistent with the results of in situ measurements that have been carried out at the Mining Institute of the Kola Science Center, Russian Academy of Sciences (RAS), for over 40 years. It is possible to forecast the horizontal stress gradient based on depth using our concept on the genesis of horizontal overpressure, and this forecasting is important for studying the formation of endogenic deposits.
Abstract: Hf isotope data for zircons and whole-rocks from lower crustal mafic granulite and pyroxenite xenoliths from NW Russia are presented together with the results of U-Pb zircon dating, Sm-Nd and Rb-Sr isotopic compositions of bulk-rocks and minerals, and trace element compositions of minerals. Most zircons preserve a record of only the youngest metamorphic events, but a few Grt-granulite xenoliths retain Archean magmatic zircons from their protolith. Metamorphic zircons have highly variable ?Hf(t) values from -25 to -4. The least radiogenic zircons were formed by recrystallization of primary magmatic Archean zircons. Zircons with the most radiogenic ?Hf grew before garnet or were contemporaneous with its formation. Zircons with ?Hf(t) from -15 to -9 formed by various mechanisms, including recrystallization of pre-existing metamorphic zircons, subsolidus growth in the presence of garnet and exsolution from rutile. They inherited their Hf isotopic composition from clinopyroxene, pargasite, rutile and earlier-formed zircon that had equilibrated with garnet. Subsolidus zircons were formed in response to a major change in mineral association (i.e. garnet- and zircon-producing reactions including partial melting). Recrystallized zircons date the onset of high-temperature conditions without a major change in mineral association. Age data for metamorphic zircons fall into five groups: >1•91 Ga, 1•81-1•86 Ga, 1•74-1•77 Ga, 1•64-1•67 Ga and <1•6 Ga. Most ages correlate with metamorphic events in the regional upper crust superimposed onto rocks of the Belomorian belt during formation of the Lapland Granulite Belt. Zircon formation and resetting at 1•64-1•67 Ga significantly postdates Lapland-Kola orogenic events and may relate to the onset of Mesoproterozoic rifting. The youngest ages (1•6-1•3 Ga) correspond to an event that affected only a few grains in some samples and can be explained by interaction with a localized fluid. The observed garnet-granulite associations were formed at 1•83 Ga in Arkhangelsk xenoliths and 1•74-1•76 Ga in most Kola xenoliths. By the end of the Lapland-Kola orogeny, the rocks were already assembled in the lower crust. However, no addition of juvenile material has been detected and preservation of pre-Lapland-Kola metamorphic zircon indicates that some xenoliths represent an older lower crust. Granulites, pyroxenites and Phl-rich rocks have a common metamorphic history since at least c. 1•75 Ga. At about 1•64 Ga metasomatic introduction of phlogopite took place; however, this was only one of several phlogopite-forming events in the lower crust.
Abstract: The crystal structure of a new structural variety of loparite (Na0.56Ce0.21La0.14Ca0.06Sr0.03Nd0.02Pr0.01)?=1.03(Ti0.83Nb0.15)?=0.98O3 from the Khibiny alkaline massif, Kola peninsula, Russia, was solved by direct methods and refined to R1 = 0.029 for 492 unique observed reflections with I > 2?(I). The mineral is orthorhombic, Ima2, a = 5.5129(2), b = 5.5129(2) and c = 7.7874(5) Å. Similarly to other perovskite-group minerals with the general formula ABO3, the crystal structure of loparite is based upon a three-dimensional framework of distorted corner-sharing BO6. The A cations are coordinated by 12 oxygen atoms and are situated in distorted cuboctahedral cavities. In contrast to the ideal perovskite-type structure (Pm3?m), the unit cell is doubled along the c axis and the a and b axes are rotated in the ab plane at 45o. The BO6 octahedron displays distortion characteristic for the d0 transition metal cations with the out-of-center shift of the B site. The symmetry reduction is also attributable to the distortion of the BO6 octahedra which are tilted and rotated with respect to the c axis. The occurrence of a new acentric variety of loparite can be explained by the pecularities of its chemical composition characterized by the increased content of Ti compared to the previously studied samples.
Pyrochlore group minerals from Paleozoic carbonatite massifs of the Kola Peninsula: composition and evolution.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 20-21.
Russia, Kola Peninsula
carbonatites
Abstract: Chemical composition and evolution of pyrochlore-group minerals (Nb?Ta?Ti) from the early phoscorites and calcite carbonatites, and late rare-earth dolomite carbonatites from Seblyavr and Vuorijarvi Paleozoic massifs have been studied. There are two trends in pyrochlore composition evolution: the change of U, Ti, and Ta enriched varieties by calcium high-Nb, and the change of early calcium varieties by barium-strontium pyrochlores. The substitutions are described by the typical reactions: 2Ti4+ + U4+ ? 2Nb5+ + Ca2+; Ta5+ ? Nb5+; U4+ + v (vacancy) ? 2Ca2+. The Ca ranges in pyrochlores are explained by isomorphic occupation of the cation position A with Ba, Sr, and REE, the total concentration of which increases as the carbonatite melt evolved and reaches a maximum in rare-earth dolomite carbonatites. The formation of barium pyrochlore is mainly due to successive crystallization from the Ba and Sr enriched melt (oscillatory zoning crystals), or with the secondary replacement of grain margins of the calcium pyrochlore, as an additional mechanism of formation. High enrichments in LREE2O3 (up to 6 wt.%) are identified. The fluorine content in pyrochlore group minerals varies widely. A high concentration (up to 8 wt.%) is found in central and marginal zones of crystals from calcite carbonatites, while it decreases in the pyrochlore from dolomite carbonatites. Fluorine in the crystal lattice has sufficient stability during cation-exchange processes and it is not lost in the case of developing of late carbonatites over the earlier ones. In the late mineral populations the relics enriched by this component are observed. There is a positive correlation of fluorine with sodium. The marginal and fractured zones of pyrochlore crystals from all rock types are represented by phases with a cation deficiency in position A and an increased Si. The evolution of mineral composition depends on the alkaline-ultramafic melt crystallization differentiation, enrichment of the late melts by alkalis and alkaline earth metals at the high fluorine activity. It is determined that the fluorine sharply increases from the early pyroxenites to the carbonatite rocks of the massif. The foscorites and carbonatites of the early stages of crystallization are the most enriched in fluorine, while the late dolomite carbonatites are depleted by this component and enriched in chlorine and water. The fluorine saturation of the early stages of carbonatite melting leads to the formation of fluorapatite and pyrochlore minerals which are the main mineralsconcentrators of fluorine. Pyrochlore group minerals from the Paleozoic carbonatite complexes of the Kola Peninsula are characterized by decreasing Pb, Th and U, and Th/U ratios in the transition from the early foscorites to later calcite carbonatites and hydrothermal dolomite carbonatites. The pyrochlore age varies within the 420-320 m.y. interval (U-Pb SHRIMPII data), while the rocks of the earliest magmatic stages has an individual grain age of 423 ± 15 Ma, but pyrochlore ages for calcite and dolomite carbonatites are younger: 351 ± 8.0 Ma and 324 ± 6.1 Ma, respectively. Such a dispersion of the age data is apparently associated with a disturbed Th/U ratio due to high ability for cation-exchange processes of pyrochlore crystalline matrix including secondary transformations. The research was done within the framework of the scientific program of Russian Academy of Sciences and state contract K41.2014.014 with Sevzapnedra.
Preservation model for Kola alkaline province for Paleozoic and Paleoproterozoic alkaline magmatism volume comparing.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 13.
Russia, Kola Peninsula
carbonatites
Abstract: Northern part of the Fennoscandian Shield in Kola Peninsula and Northern Karelia was intruded by alkaline magmatic complexes during the two main episodes. Paleoproterozoic alkaline province consisting from five alkaline massifs and Paleozoic alkaline province, consisting from twenty alkaline-ultramafic rock complexes, together with two giant nepheline syenite complexes are practically overlap. Based on the data about morphology and internal structure of the Paleozoic alkaline and ultramaficcarbonatite intrusions and their average denudation rates, the model of alkaline province destruction was developed. This model allows forecasting, how many intrusions of Kola Paleozoic alkaline province will remain and calculate preservation ratio for any moment of future. The dependence of preservation ratio on the age of province allow to compare the initial numbers of massifs in alkaline provinces and conclude that Paleoproterozoic event of alkaline magmatism in Kola peninsula was even more powerful than Paleozoic one.
Abstract: Hf isotope data for zircons and whole-rocks from lower crustal mafic granulite and pyroxenite xenoliths from NW Russia are presented together with the results of U-Pb zircon dating, Sm-Nd and Rb-Sr isotopic compositions of bulk-rocks and minerals, and trace element compositions of minerals. Most zircons preserve a record of only the youngest metamorphic events, but a few Grt-granulite xenoliths retain Archean magmatic zircons from their protolith. Metamorphic zircons have highly variable ?Hf(t) values from -25 to -4. The least radiogenic zircons were formed by recrystallization of primary magmatic Archean zircons. Zircons with the most radiogenic ?Hf grew before garnet or were contemporaneous with its formation. Zircons with ?Hf(t) from -15 to -9 formed by various mechanisms, including recrystallization of pre-existing metamorphic zircons, subsolidus growth in the presence of garnet and exsolution from rutile. They inherited their Hf isotopic composition from clinopyroxene, pargasite, rutile and earlier-formed zircon that had equilibrated with garnet. Subsolidus zircons were formed in response to a major change in mineral association (i.e. garnet- and zircon-producing reactions including partial melting). Recrystallized zircons date the onset of high-temperature conditions without a major change in mineral association. Age data for metamorphic zircons fall into five groups: >1•91 Ga, 1•81-1•86 Ga, 1•74-1•77 Ga, 1•64-1•67 Ga and <1•6 Ga. Most ages correlate with metamorphic events in the regional upper crust superimposed onto rocks of the Belomorian belt during formation of the Lapland Granulite Belt. Zircon formation and resetting at 1•64-1•67 Ga significantly postdates Lapland-Kola orogenic events and may relate to the onset of Mesoproterozoic rifting. The youngest ages (1•6-1•3 Ga) correspond to an event that affected only a few grains in some samples and can be explained by interaction with a localized fluid. The observed garnet-granulite associations were formed at 1•83 Ga in Arkhangelsk xenoliths and 1•74-1•76 Ga in most Kola xenoliths. By the end of the Lapland-Kola orogeny, the rocks were already assembled in the lower crust. However, no addition of juvenile material has been detected and preservation of pre-Lapland-Kola metamorphic zircon indicates that some xenoliths represent an older lower crust. Granulites, pyroxenites and Phl-rich rocks have a common metamorphic history since at least c. 1•75 Ga. At about 1•64 Ga metasomatic introduction of phlogopite took place; however, this was only one of several phlogopite-forming events in the lower crust.
Kampelite, Ba3Mg1.5,Sc4(PO4)6(OH)3.4H2O, a new very complex Ba-Sc phosphate mineral from the Kovdor phoscorite-carbonatite complex ( Kola Peninsula) Russia.
Journal of Analytical At. Spectrometry, Vol. 33, pp. 231-239.
United States, Arkansas, China, Hebei, Russia, Kola Peninsula, Europe, Sweden, Canada, Ontario
geochronology
Abstract: We report the first U-Pb geochronological investigation of schorlomite garnet from carbonatite and alkaline complexes and demonstrate its applicability for U-Pb age determination using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) due to its relatively high U and Th abundances and negligible common Pb content. The comparative matrix effects of laser ablation of zircon and schorlomite are investigated and demonstrate the necessity of a suitable matrix-matched reference material for schorlomite geochronology. Laser-induced elemental fractional and instrumental mass discrimination were externally-corrected using an in house schorlomite reference material (WS20) for U-Pb geochronology. In order to validate the effectiveness and robustness of our analytical protocol, we demonstrate the veracity of U-Pb age determination for five schorlomite samples from: the Magnet Cove complex, Arkansas (USA); the Fanshan ultrapotassic complex, Hebei (China); the Ozernaya alkaline ultramafic complex, Kola Peninsula (Russia); the Alnö alkaline-rock carbonatite complex (Sweden); and the Prairie Lake carbonatite complex, Ontario (Canada). The schorlomite U-Pb ages range from 96 Ma to 1160 Ma, and are almost identical to ages determined from other accessory minerals in these complexes and support the reliability of our analytical protocol. Schorlomite garnet U-Pb geochronology is considered to be a promising new technique for understanding the genesis of carbonatites, alkaline rocks, and related rare-metal deposits.
Abstract: Comprehensive research of ore-bearing differentiated intrusions of the Keulik-Kenirim structural unit, which represents a fragment of the Paleoproterozoic Pechenga-Varzuga Belt, has been carried out for the first time. The intrusions are subvolcanic by type and lenticular in shape, nearly conformable and steeply dipping. They are made up of peridotite, olivine and plagioclase pyroxenites, and gabbro metamorphosed under amphibolite facies conditions along with host basic volcanics. All intrusive rocks are enriched in TiO2 and FeO. Sulfide Cu-Ni mineralization is represented by disseminated, pocket, and stringer-disseminated types, which are clustered in the peridotitic zone as hanging units and bottom lodes. The Ni content in disseminated ore is estimated at 0.45-0.55 wt % and 1.15-3.32 wt % in ore pockets; the Cu grades are 0.17-0.20 and 0.46-5.65 wt %, respectively. To determine the age of intrusions and metamorphism of intrusive and volcanic rocks, various isotopic systems have been used: Sm-Nd (TIMS) in rock and U-Pb (SIMS SHRIMP) and Lu-Hf (LA-ICP-MS) in zircon. Conclusions on the origin of zircons are based on concentrations of trace elements including REE therein and Hf-Nd correlation in zircons and rocks. The U-Pb system of zircons reflects episodes of igneous rock formation (1982 ± 12 Ma) and their postmagmatic transformation (1938 ± 20 Ma). The last disturbance of the U-Pb isotopic system occurred 700 and 425 Ma. Xenogenic zircons dated from 3.17 to 2.65 Ga have been revealed in the studied samples. These zircons were captured by magma from the Archean basement during its ascent. The intrusions were emplaced synchronously with economic ore formation in the Pechenga ore field (1985 ± 10 Ma). The peak metamorphism of intrusive rocks under amphibolite facies conditions is recorded at 40 Ma later. The differentiated intrusions of the Keulik-Kenirim structural unit are close in their internal structure, mineralogy, and geochemistry, as well as in age and features of related Cu-Ni mineralization to ore-bearing intrusions of the Pechenga ore field, which are derivatives of ferropicritic (ferriferous) magmatism.
Mineralogical Magazine, Vol. 82, no. 2, pp. 329-346.
Russia, Kola Peninsula
deposit - Kovdor
Abstract: Two quintinite polytypes, 3R and 2T, which are new for the Kovdor alkaline-ultrabasic complex, have been structurally characterized. The crystal structure of quintinite-2T was solved by direct methods and refined to R1 = 0.048 on the basis of 330 unique reflections. The structure is trigonal, P c1, a = 5.2720(6), c = 15.113(3) Å and V = 363.76(8) Å3. The crystal structure consists of [Mg2Al(OH)6]+ brucite-type layers with an ordered distribution of Mg2+ and Al3+ cations according to the × superstructure with the layers stacked according to a hexagonal type. The complete layer stacking sequence can be described as …=Ab1C = Cb1A=…. The crystal structure of quintinite-3R was solved by direct methods and refined to R1 = 0.022 on the basis of 140 unique reflections. It is trigonal, R m, a = 3.063(1), c = 22.674(9) Å and V = 184.2(1) Å3. The crystal structure is based upon double hydroxide layers [M2+,3+(OH)2] with disordered distribution of Mg, Al and Fe and with the layers stacked according to a rhombohedral type. The stacking sequence of layers can be expressed as …=?B = BC = CA=… The study of morphologically different quintinite generations grown on one another detected the following natural sequence of polytype formation: 2H ? 2T ? 1M that can be attributed to a decrease of temperature during crystallization. According to the information-based approach to structural complexity, this sequence corresponds to the increasing structural information per atom (IG): 1.522 ? 1.706 ? 2.440 bits, respectively. As the IG value contributes negatively to the configurational entropy of crystalline solids, the evolution of polytypic modifications during crystallization corresponds to the decreasing configurational entropy. This is in agreement with the general principle that decreasing temperature corresponds to the appearance of more complex structures.
Abstract: Melt/fluid inclusions in diamonds provide important evidence for mantle diamond-forming fluids or melts. By now, the major characteristics of the composition of microinclusions have been analyzed in diamonds from several kimberlite provinces and pipes worldwide [1-4]. Here we report the first data on the composition of parent diamondforming melts for diamonds from the Arkhangelsk kimberlite province. After the study of morphology, specialty of the internal structure, and distribution of microinclusions in diamonds, 10 single crystals were selected from the 31 diamonds of the representative collection. The studied crystals may be divided into two groups: cuboids and coated diamonds. The crystals have grayish yellow or dark gray colors and are almost nontransparent due to the high content of microinclusions. Polished slices of these diamonds were studied by IR-spectroscopy, which allowed us to calculate the content of nitrogen defects, as well as the content of water and carbonates in microinclusions. X-ray spectral analyses allowed to study the composition of fluid/melt microinclusions and showed that they were essentially carbonate-silicate with significant variations between these two end-members. All inclusions contain water, with the highest H2O/CO2 in highly siliceous inclusions. Unlike diamonds from Canada and South Africa [1, 2], the studied inclusions in diamionds from the Arkhangelsk province are almost free of chlorides. Comparison of the data obtained with the database on fliud/melt inclusions in diamonds worldwide shows similar of Arkhangelsk diamonds to some diamonds from Yakutia [3, 4], and the data obtained are the most similar to the composition of microinclusions in diamonds from the Internatsionalnaya pipe (Yakutia).
Physics and Chemistry of Minerals, Vol. 45, pp. 745-758.
Russia, Kola Peninsula
alkaline
Abstract: The new eudialyte-group mineral siudaite, ideally Na8(Mn2+2Na)Ca6Fe3+3Zr3NbSi25O74(OH)2Cl•5H2O, was discovered in a peralkaline pegmatite situated at the Eveslogchorr Mt., Khibiny alkaline massif, Kola Peninsula, Russia. The associated minerals are aegirine, albite, microcline, nepheline, astrophyllite, and loparite-(Ce). Siudaite forms yellow to brownish-yellow equant anhedral grains up to 1.5 cm across. Its lustre is vitreous, and the streak is white. Cleavage is none observed. The Mohs’ hardness is 4½. Density measured by hydrostatic weighing is 2.96(1) g/cm3. Density calculated using the empirical formula is equal to 2.973 g/cm3. Siudaite is nonpleochroic, optically uniaxial, negative, with ??=?1.635(1) and ??=?1.626(1) (??=?589 nm). The IR spectrum is given. The chemical composition of siudaite is (wt%; electron microprobe, H2O determined by HCN analysis): Na2O 8.40, K2O 0.62, CaO 9.81, La2O3 1.03, Ce2O3 1.62, Pr2O3 0.21, Nd2O3 0.29, MnO 6.45, Fe2O3 4.51. TiO2 0.54, ZrO2 11.67, HfO2 0.29, Nb2O5 2.76, SiO2 47.20, Cl 0.54, H2O 3.5, -O?=?Cl ??0.12, total 99.32. According to Mössbauer spectroscopy data, all iron is trivalent. The empirical formula (based on 24.5 Si atoms pfu, in accordance with structural data) is [Na7.57(H2O)1.43]?9(Mn1.11Na0.88Ce0.31La0.20Nd0.05Pr0.04K0.41)?3(H2O)1.8(C a5.46Mn0.54)?6(Fe3+1.76Mn2+1.19)?2.95Nb0.65(T i0.20Si0.50)?0.71(Zr2.95Hf0.04Ti0.01)?3Si24.00Cl0.47O70(OH)2Cl0.47•1.2H2O. The crystal structure was determined using single-crystal X-ray diffraction data. The new mineral is trigonal, space group R3m, with a?=?14.1885(26) Å, c?=?29.831(7) Å, V?=?5200.8(23) Å3 and Z?=?3. Siudaite is chemically related to georgbarsanovite and is its analogue with Fe3+-dominant M2 site. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 6.38 (60) (-114), 4.29 (55) (-225), 3.389 (47) (131), 3.191 (63) (-228). 2.963 (100) (4-15), 2.843 (99) (-444), 2.577 (49) (3-39). Siudaite is named after the Polish mineralogist and geochemist Rafa? Siuda (b. 1975).
Contributions to Mineralogy and Petrology, Vol. 173, 12, pp. 106-
Russia, Kola Peninsula
deposit - Afrikanda
Abstract: Perovskite is a common accessory mineral in a variety of mafic and ultramafic rocks, but perovskite deposits are rare and studies of perovskite ore deposits are correspondingly scarce. Perovskite is a key rock-forming mineral and reaches exceptionally high concentrations in olivinites, diverse clinopyroxenites and silicocarbonatites in the Afrikanda alkaline-ultramafic complex (Kola Peninsula, NW Russia). Across these lithologies, we classify perovskite into three types (T1-T3) based on crystal morphology, inclusion abundance, composition, and zonation. Perovskite in olivinites and some clinopyroxenites is represented by fine-grained, equigranular, monomineralic clusters and networks (T1). In contrast, perovskite in other clinopyroxenites and some silicocarbonatites has fine- to coarse-grained interlocked (T2) and massive (T3) textures. Electron backscatter diffraction reveals that some T1 and T2 perovskite grains in the olivinites and clinopyroxenites are composed of multiple subgrains and may represent stages of crystal rotation, coalescence and amalgamation. We propose that in the olivinites and clinopyroxenites, these processes result in the transformation of clusters and networks of fine-grained perovskite crystals (T1) to mosaics of more coarse-grained (T2) and massive perovskite (T3). This interpretation suggests that sub-solidus processes can lead to the development of coarse-grained and massive perovskite. A combination of characteristic features identified in the Afrikanda perovskite (equigranular crystal mosaics, interlocked irregular-shaped grains, and massive zones) is observed in other oxide ore deposits, particularly in layered intrusions of chromitites and intrusion-hosted magnetite deposits and suggests that the same amalgamation processes may be responsible for some of the coarse-grained and massive textures observed in oxide deposits worldwide.
European Journal of Mineralogy, Vol. 31, pp. 13-143.
Russia, Kola Peninsula
deposit - Khibiny
Abstract: The new mineral alexkhomyakovite K6(Ca2Na)(CO3)5Cl?6H2O (IMA2015-013) occurs in a peralkaline pegmatite at Mt. Koashva, Khibiny alkaline complex, Kola peninsula, Russia. It is a hydrothermal mineral associated with villiaumite, natrite, potassic feldspar, pectolite, sodalite, biotite, lamprophyllite, titanite, fluorapatite, wadeite, burbankite, rasvumite, djerfisherite, molybdenite and an incompletely characterized Na-Ca silicate. Alexkhomyakovite occurs as equant grains up to 0.2 mm, veinlets up to 3 cm long and up to 1 mm thick and fine-grained aggregates replacing delhayelite. Alexkhomyakovite is transparent to translucent, colourless, white or grey, with vitreous to greasy lustre. It is brittle, the Mohs hardness is ca. 3. No cleavage was observed, the fracture is uneven. D meas = 2.25(1), D calc = 2.196 g cm?3. Alexkhomyakovite is optically uniaxial (-), ? = 1.543(2), ? = 1.476(2). The infrared spectrum is reported. The chemical composition [wt%, electron microprobe data, CO2 and H2O contents calculated for 5 (CO3) and 6 (H2O) per formula unit (pfu), respectively] is: Na2O 4.09, K2O 35.72, CaO 14.92, MnO 0.01, FeO 0.02, SO3 0.11, Cl 4.32, CO2 28.28, H2O 13.90, -O=Cl -0.98, total 100.39. The empirical formula calculated on the basis of 9 metal cations pfu is K5.90Ca2.07Na1.03(CO3)5(SO4)0.01O0.05Cl0.95?6H2O. The numbers of CO3 groups and H2O molecules are based on structure data. Alexkhomyakovite is hexagonal, P63/mcm, a = 9.2691(2), c = 15.8419(4) Å, V = 1178.72(5) Å3 and Z = 2. The strongest reflections of the powder X-ray diffraction pattern [d Å(I)(hkl)] are: 7.96(27)(002), 3.486(35)(113), 3.011(100)(114), 2.977(32)(211), 2.676(36)(300), 2.626(42)(213, 115), 2.206(26)(311) and 1.982(17)(008). The crystal structure (solved from single-crystal X-ray diffraction data, R = 0.0578) is unique. It is based on (001) heteropolyhedral layers of pentagonal bipyramids (Ca,Na)O5(H2O)2 interconnected via carbonate groups of two types, edge-sharing ones and vertex-sharing ones. Ca and Na are disordered. Ten-fold coordinated K cations centre KO6Cl(H2O)3 polyhedra on either side of the heteropolyhedral layer. A third type of carbonate group and Cl occupy the interlayer. The mineral is named in honour of the outstanding Russian mineralogist Alexander Petrovich Khomyakov (1933-2012).
Abstract: The structure, geochemistry, and U-Pb and Lu-Hf isotopic composition of zircon crystals from garnet granulite xenoliths of the lower crust in the Belomorian mobile belt have been studied. It has been established that Early Paleoproterozoic zircon, 2.47 Ga in age, is primary magmatic and formed during crystallization of mafic rocks in the lower crust. Meso- and Neoarchean zircons are xenogenic crystals trapped by mafic melt during its contamination with older crustal sialic rocks. Metamorphic zircon grains have yielded a Late Paleoproterozoic age (1.75 Ga). A Paleozoic age has been established for a magmatic crystal formed due to interaction of xenoliths with an alkaline ultramafic melt, which delivered xenoliths to surface. The U-Pb datings and Lu-Hf systematics of crystals have been used to delineate the stages of formation and transformation of the lower crust in this region.
Abstract: Hydroxynatropyrochlore, (Na,?a,Ce)2Nb2O6(OH), is a new Na-Nb-OH-dominant member of the pyrochlore supergroup from the Kovdor phoscorite-carbonatite pipe (Kola Peninsula, Russia). It is cubic, Fd-3m, a = 10.3211(3) Å, V = 1099.46 (8) Å3, Z = 8 (from powder diffraction data) or a = 10.3276(5) Å, V = 1101.5(2) Å3, Z = 8 (from single-crystal diffraction data). Hydroxynatropyrochlore is a characteristic accessory mineral of low-carbonate phoscorite of the contact zone of the phoscorite-carbonatite pipe with host foidolite as well as of carbonate-rich phoscorite and carbonatite of the pipe axial zone. It usually forms zonal cubic or cubooctahedral crystals (up to 0.5 mm in diameter) with irregularly shaped relics of amorphous U-Ta-rich hydroxykenopyrochlore inside. Characteristic associated minerals include rockforming calcite, dolomite, forsterite, hydroxylapatite, magnetite,and phlogopite, accessory baddeleyite, baryte, barytocalcite, chalcopyrite, chamosite-clinochlore, galena, gladiusite, juonniite, ilmenite, magnesite, pyrite, pyrrhotite, quintinite, spinel, strontianite, valleriite, and zirconolite. Hydroxynatropyrochlore is pale-brown, with an adamantine to greasy lustre and a white streak. The cleavage is average on {111}, the fracture is conchoidal. Mohs hardness is about 5. In transmitted light, the mineral is light brown, isotropic, n = 2.10(5) (??= 589 nm). The calculated and measured densities are 4.77 and 4.60(5) g•cm-3, respectively. The mean chemical composition determined by electron microprobe is: F 0.05, Na2O 7.97, CaO 10.38, TiO2 4.71, FeO 0.42, Nb2O5 56.44, Ce2O3 3.56, Ta2O5 4.73, ThO2 5.73, UO2 3.66, total 97.65 wt. %. The empirical formula calculated on the basis of Nb+Ta+Ti = 2 apfu is (Na1.02Ca0.73Ce0.09Th0.09 U0.05Fe2+0.02)?2.00 (Nb1.68Ti0.23Ta0.09)?2.00O6.03(OH1.04F0.01)?1.05. The simplified formula is (Na, Ca,Ce)2Nb2O6(OH). The mineral slowly dissolves in hot HCl. The strongest X-ray powderdiffraction lines [listed as (d in Å)(I)(hkl)] are as follows: 5.96(47)(111), 3.110(30)(311), 2.580(100)(222), 2.368(19)(400), 1.9875(6)(333), 1.8257(25)(440) and 1.5561(14)(622). The crystal structure of hydroxynatropyrochlore was refined to R1 = 0.026 on the basis of 1819 unique observed reflections. The mineral belongs to the pyrochlore structure type A2B2O6Y1 with octahedral framework of corner-sharing BO6 octahedra with A cations and OH groups in the interstices. The Raman spectrum of hydroxynatropyrochlore contains characteristic bands of the lattice, BO6, B-O and O-H vibrations and no characteristic bands of the H2O vibrations. Within the Kovdor phoscorite-carbonatite pipe, hydroxynatropyrochlore is the latest hydrothermal mineral of the pyrochlore supergroup, which forms external rims around grains of earlier U-rich hydroxykenopyrochlore and separated crystals in voids of dolomite carbonatite veins. The mineral is named in accordance with the pyrochlore supergroup nomenclature.
Abstract: The Paleoproterozoic Lapland-Kola Orogen in Fennoscandia has been studied for decades and several plate tectonic models have been proposed including one-sided subduction zone, either towards SW or NW, or two opposite-verging subduction zones before the collision. Based on new structural and isotope data from Finland and recently published data from Russia, we propose a revised tectonic model for the Paleoproterozoic Lapland-Kola Orogen. The main components are foreland in the NE followed by cryptic suture, Inari arc, retro-arc basin and retro-arc foreland in the SW. The latter three constitute the Inari Orocline.
Subduction towards present SW and subsequent arc magmatism (Inari arc) started at ca. 1.98?Ga followed by voluminous sedimentation in the deepening retro-arc basin. Underplating of a mid-ocean ridge caused flat subduction and magmatic flare at 1.92?Ga over a broad distance in the retro-arc basin. Rapid heating led to melting of the retro-arc basin sediments and voluminous amounts of granulite-facies diatexites formed. During collision (D1) at 1915-1910?Ma, large thrust nappes formed on the foreland. Deformation in the retro-arc basin is seen as recumbent folding and shearing of diatexites in the lower parts of the basin and thrusting of metatextite-diatexite packages in the upper parts. A post-collisional stage is seen as 1904?Ma appinites and decompression derived granites at 1.90-1.89?Ga. Renewed shortening (D2), due to far-field effects in SW at 1.88-1.87?Ga, led to thick-skin shortening of the Archean middle crust, large-scale crustal duplexing of already cooled granulites towards the retro-arc foreland and inclined upright folding of granulites in the opposite direction towards the Inari arc. A switch in the stress field from NE-SW to NW-SE led to orogen-parallel contraction and buckling started along a dextral strike-slip fault zone to form the Inari Orocline. Buckling is seen in the bending of pre-orocline fabrics and formation of syn-orocline fabrics: radial conical folds (D3), radial fractures, a strike-slip fault zone and thrusting at the hinge zone. The end-result is a mega-scale parallel multi-layer fold composed of the Inari arc, retro-arc basin and possibly also the heated retro-arc foreland.
Abstract: Results from thermochronological studies have multiple applications to various problems in tectonics and landform evolution However, up to now a lack of thermochronological data from the northeastern Fennoscandian Shield has complicated the interpretation of tectonothermal evolution of the region Here, we use both new and previously published multimineral 40Ar/39Ar data (amphibole, mica, and feldspar) on the various Precambrian magmatic and metamorphic complexes to reconstruct the thermal history of NE Fennoscandia within the Kola Peninsula area in the interval 1900–360 Ma Using the apatite fission track method as well as a numerical model of the heating?cooling process of northeastern Fennoscandia's upper crust, we have reconstructed its thermal evolution for the interval 360–0 Ma According to our model, since Lapland?Kola orogenesis (1930–1905 Ma) northeastern Fennoscandia experienced a quasi?monotonous cooling with the average rate of ~0 15 °C/Myr, which is equal to an exhumation rate of ~1–2 m/Myr New apatite fission track data and time?temperature modeling reveal a “hidden” endogenous thermal event in the NE Fennoscandia that took place between 360 and 300 Ma This we attribute to an elevated geothermal gradient due to Baltica's drift over the African large low shear?wave velocity province in the lowest mantle and/or thermal blanketing by insulating Devonian?Carboniferous sedimentary/volcanic cover Our model is further supported by evidence of Late Devonian?Carboniferous rifting in the East and South?Western Barents Basin, as well as various 360–300 Ma magmatic events within SW Fennoscandia and the Baltic countries
Abstract: Results from thermochronological studies have multiple applications to various problems in tectonics and landform evolution. However, up to now a lack of thermochronological data from the northeastern Fennoscandian Shield has complicated the interpretation of tectonothermal evolution of the region. Here, we use both new and previously published multimineral 40Ar/39Ar data (amphibole, mica, and feldspar) on the various Precambrian magmatic and metamorphic complexes to reconstruct the thermal history of NE Fennoscandia within the Kola Peninsula area in the interval 1900-360 Ma. Using the apatite fission track method as well as a numerical model of the heating?cooling process of northeastern Fennoscandia's upper crust, we have reconstructed its thermal evolution for the interval 360-0 Ma. According to our model, since Lapland?Kola orogenesis (1930-1905 Ma) northeastern Fennoscandia experienced a quasi?monotonous cooling with the average rate of ~0.15 °C/Myr, which is equal to an exhumation rate of ~1-2 m/Myr. New apatite fission track data and time?temperature modeling reveal a “hidden” endogenous thermal event in the NE Fennoscandia that took place between 360 and 300 Ma. This we attribute to an elevated geothermal gradient due to Baltica's drift over the African large low shear?wave velocity province in the lowest mantle and/or thermal blanketing by insulating Devonian?Carboniferous sedimentary/volcanic cover. Our model is further supported by evidence of Late Devonian?Carboniferous rifting in the East and South?Western Barents Basin, as well as various 360-300 Ma magmatic events within SW Fennoscandia and the Baltic countries.
Abstract: Detailed studies have shown that a change in the eudialyte occurrence forms (and the moment of its crystallization) is a new geochemical criterion for rare metal ore content in alkalic magmas (eudialyte ores). A new principle of the presence of ores in alkalic magmas has been formulated: a prerequisite for the formation of an ore deposit is early saturation of alkalic magmas with an ore mineral. If the ore component concentration is significantly lower than the cotectic (saturation), then melt saturation and crystallization of an ore mineral will take place at later stages of rock formation in a small volume of the interstitial melt, when the phenomena of convective?gravity differentiation and segregation of mineral phases in the form of ore deposits are hampered. This leads to dispersion of the ore components in the form of xenomorphic grains of accessory minerals. Rocks of the differentiated complex (lower zone of the Lovozero deposit) and rocks of the Khibiny massif contain xenomorphic eudialyte and are not promising for eudialyte ores. Eudialyte deposits are associated with the upper zone of the Lovozero intrusion where euhedral early eudialyte occurs. The initial magma is saturated with eudialyte after crystallization of about 80% of the intrusion. The proposed criterion is applicable to the largest alkalic massifs in the world. The Ilimaussaq massif (Greenland), the rocks of which contain early crystallized, euhedral eudialyte, hosts a superlarge eudialyte ore deposit. Unlike the Khibiny massif and the Pilanesberg alkalic complex, the rocks of which contain late xenomorphic eudialyte, this massif has no deposits of this type.
Geology of Ore Deposits, Vol. 61, 7, pp. 581-588. pdf
Russia, Kola Peninsula
magmatism
Abstract: The Neoarchean subalkaline magmatism of the Keivy structure is expressed in the formation of the volcanoplutonic latite-monzonite-granite association (LMGA). The formation of LMGA magmas is assumed to occur due to melting of metasomatically altered mafic rocks during intrusion into the lower crust of basaltic melts initial for rocks of the dike complex and gabbro-labradorite massifs. The alkaline granites associated with LMGA have a close U-Pb age but a later formation time based on the geological data. With respect to LMGA, alkali granites have increased concentrations of SiO2, alkalis (K2O/Na2O = 1.1-1.4), iron (F# = 84-98%), a high agpaitic index (Kagp = 0.86-1.2), and lower quantities of TiO2, MgO, Fetot, and Al2O3, which probably resulted from the higher degree of differentiation of their initial melts compared to LMGA.
Abstract: Rifting, breakup, and subsequent collision related to the ca. 1.92-1.79?Ga Svecofennian orogeny fragmented and deformed the western margin of the Archean Karelia-Kola craton into four crustal blocks: Pudasjärvi, Iisalmi, Kuhmo, and Taivalkoski. Detailed quantification of Svecofennian deformation is limited due to poorly exposed basement geology and an as yet incomplete dyke swarm record. New U-Pb ID-TIMS geochronological results on baddeleyite and zircon are presented for three key mafic dykes from the Pudasjärvi block, namely the Uolevinlehto, Myllykangas, and Sipojuntti dykes. The age of the 325°-trending Uolevinlehto dyke is estimated at ca. 2400?±?12?Ma from discordant multigrain baddeleyite fractions, showing it to be younger than ca. 2450?Ma dykes across Karelia. The 350°-trending Myllykangas dyke has a minimum age of 2135.2?+?3.6/?3.7?Ma based on chemically abraded zircon. Results from single baddeleyite grains provide a precise upper intercept age of 2128.9?±?1.2?Ma for the 320°-trending Sipojuntti dyke. Our new U-Pb ages are integrated with those from the literature to define six major dyke swarms in the Pudasjärvi block: the WNW-trending ca. 2.45?Ga Pääjärvi, NW-trending ca. 2.40?Ga Uolevinlehto, NW-trending ca. 2.13-2.10?Ga Tohmajärvi, WNW-trending ca. 2.07?Ga Palomaa, NNW-trending ca. 1.98?Ga Paukkajanvaara and undated"East-West" dykes. Trends of contemporaneous dyke swarms in the Taivalkoski and Kuhmo blocks, however, are systematically offset by 35°. With subvertical dips, offset dyke swarms record 35° clockwise vertical-axis rotation of the Pudasjärvi block relative to the interior of Karelia, consistent with dextral transpression during the Svecofennian orogeny. Structural restoration of the Pudasjärvi blocks improves the constraints on regional dyke swarm patterns, and these are used to revise the position of the Karelia-Kola craton within the context of the paleogeographic reconstruction of supercraton Superia.
Abstract: New data on the age of dolerite dikes in the NE part of the Kola province of the Fennoscandinavian shield and the picrodolerite sills that cut the dikes are presented. The results of U-Pb ID-TIMS baddeleyite dating indicate that dolerites were formed between 2508 ± 6 and 2513 ± 16 Ma ago, simultaneously with the intrusions of the Monchegorsk group. A comparison of the composition of the dolerites studied with dykes of the same age found in other Archean cratons shows their significant similarity and suggests their formation at the same large magmatic province. The age of baddeleyite from the picrodolerites sills at 2403 ± 12 Ma ago indicates an event of basic magmatism that was not previously established in this part of the Fennoscandinavian shield. It is possible that, along with dolerite dykes with an age of 2405 Ma and komatiites of the Vetreny belt of the Karelian craton, sills of the Kola province are a component of a unified large magmatic event.
Europe, Fennoscandia, Kola Peninsula, Karelia, Canada
craton
Abstract: Rapid glacio-isostatic rebound in Fennoscandia and Canada that is nonuniform in time and space indicates that there is a layer with strongly decreased viscosity at shallow crustal depths. The upper boundary of the layer is near the depth of 15 km, which corresponds to the maximum depth of earthquake hypocenters in the Precambrian cratons of the Kola Peninsula and Karelia. The position of the lower boundary is less distinct; however, most likely it is located near the base of the crust. The formation of such a layer in the Pliocene-Quaternary occurred due to infiltration of a large volume of mantle fluids into the crust. In many regions, this has led to retrograde metamorphism with rock expansion and a strong decrease in rocks viscosity.
Abstract: We present petrography and mineral chemistry for both phlogopite, from mantle-derived xenoliths (garnet peridotite, eclogite and clinopyroxene-phlogopite rocks) and for megacryst, macrocryst and groundmass flakes from the Grib kimberlite in the Arkhangelsk diamond province of Russia to provide new insights into multi-stage metasomatism in the subcratonic lithospheric mantle (SCLM) and the origin of phlogopite in kimberlite. Based on the analysed xenoliths, phlogopite is characterized by several generations. The first generation (Phl1) occurs as coarse, discrete grains within garnet peridotite and eclogite xenoliths and as a rock-forming mineral within clinopyroxene-phlogopite xenoliths. The second phlogopite generation (Phl2) occurs as rims and outer zones that surround the Phl1 grains and as fine flakes within kimberlite-related veinlets filled with carbonate, serpentine, chlorite and spinel. In garnet peridotite xenoliths, phlogopite occurs as overgrowths surrounding garnet porphyroblasts, within which phlogopite is associated with Cr-spinel and minor carbonate. In eclogite xenoliths, phlogopite occasionally associates with carbonate bearing veinlet networks. Phlogopite, from the kimberlite, occurs as megacrysts, macrocrysts, microcrysts and fine flakes in the groundmass and matrix of kimberlitic pyroclasts. Most phlogopite grains within the kimberlite are characterised by signs of deformation and form partly fragmented grains, which indicates that they are the disintegrated fragments of previously larger grains. Phl1, within the garnet peridotite and clinopyroxene-phlogopite xenoliths, is characterised by low Ti and Cr contents (TiO2 < 1 wt.%, Cr2O3 < 1 wt.% and Mg# = 100 × Mg/(Mg + Fe) > 92) typical of primary peridotite phlogopite in mantle peridotite xenoliths from global kimberlite occurrences. They formed during SCLM metasomatism that led to a transformation from garnet peridotite to clinopyroxene-phlogopite rocks and the crystallisation of phlogopite and high-Cr clinopyroxene megacrysts before the generation of host-kimberlite magmas. One of the possible processes to generate low-Ti-Cr phlogopite is via the replacement of garnet during its interaction with a metasomatic agent enriched in K and H2O. Rb-Sr isotopic data indicates that the metasomatic agent had a contribution of more radiogenic source than the host-kimberlite magma. Compared with peridotite xenoliths, eclogite xenoliths feature low-Ti phlogopites that are depleted in Cr2O3 despite a wider range of TiO2 concentrations. The presence of phlogopite in eclogite xenoliths indicates that metasomatic processes affected peridotite as well as eclogite within the SCLM beneath the Grib kimberlite. Phl2 has high Ti and Cr concentrations (TiO2 > 2 wt.%, Cr2O3 > 1 wt.% and Mg# = 100 × Mg/(Mg + Fe) < 92) and compositionally overlaps with phlogopite from polymict breccia xenoliths that occur in global kimberlite formations. These phlogopites are the product of kimberlitic magma and mantle rock interaction at mantle depths where Phl2 overgrew Phl1 grains or crystallized directly from stalled batches of kimberlitic magmas. Megacrysts, most macrocrysts and microcrysts are disintegrated phlogopite fragments from metasomatised peridotite and eclogite xenoliths. Fine phlogopite flakes within kimberlite groundmass represent mixing of high-Ti-Cr phlogopite antecrysts and high-Ti and low-Cr kimberlitic phlogopite with high Al and Ba contents that may have formed individual grains or overgrown antecrysts. Based on the results of this study, we propose a schematic model of SCLM metasomatism involving phlogopite crystallization, megacryst formation, and genesis of kimberlite magmas as recorded by the Grib pipe.
Abstract: The Vuoriyarvi Devonian alkaline-ultramafic complex (northwest Russia) contains magnesiocarbonatites with rare earth mineralization localized in the Petyayan-Vara area. High concentrations of rare earth elements are found in two types of these rocks: (a) ancylite-dominant magnesiocarbonatites with ancylite-baryte-strontianite-calcite-quartz (±late Ca-Fe-Mg carbonates) ore assemblage, i.e., “ancylite ores”; (b) breccias of magnesiocarbonatites with a quartz-bastnäsite matrix (±late Ca-Fe-Mg carbonates), i.e., “bastnäsite ores.” We studied fluid inclusions in quartz and late-stage Ca-Fe-Mg carbonates from these ore assemblages. Fluid inclusion data show that ore-related mineralization was formed in several stages. We propose the following TX evolution scheme for ore-related processes: (1) the formation of ancylite ores began under the influence of highly concentrated (>50 wt.%) sulphate fluids (with thenardite and anhydrite predominant in the daughter phases of inclusions) at a temperature above300-350 °C; (2) the completion of the formation of ancylite ores and their auto-metasomatic alteration occurred under the influence of concentrated (40-45 wt.%) carbonate fluids (shortite and synchysite-Ce in fluid inclusions) at a temperature above 250-275 °C; (3) bastnäsite ores deposited from low-concentrated (20-30 wt.%) hydrocarbonate-chloride fluids (halite, nahcolite, and/or gaylussite in fluid inclusions) at a temperature of 190-250 °C or higher. Later hydrothermal mineralization was related to the low-concentration hydrocarbonate-chloride fluids (<15 wt.% NaCl-equ.) at 150-200 °C. The presented data show the specific features of the mineral and fluid evolution of ore-related late-stage hydrothermal rare earth element (REE) mineralization of the Vuoriyarvi alkaline-ultramafic complex.
Abstract: New petrographic, geochemical, and isotopic (Sr, Nd, and ?18?) data on olivine and pyroxene phenocrysts provide constraints on the composition and crustal evolution of primary melts of Paleoproterozoic (2.40 Ga) picrodoleritic sills in the northwest Kola province, Fennoscandian Shield. The picrodolerites form differentiated sills with S-shaped compositional profiles. Their chilled margins comprise porphyritic picrodolerite (upper margin) and olivine gabbronorite (bottom) with olivine and clinopyroxene phenocrysts. Analysis of the available data allows us to recognize three main stages in the crystallization of mineral assemblages. The central parts of large (up to 2 mm) olivine phenocrysts (Ol-1-C) crystallized at the early stage. This olivine (Mg# 85-92) is enriched in Ni (from 2845 to 3419 ppm), has stable Ni/Mg ratio, low Ti, Mn and Co concentrations, and contains tiny (up to 10 ?m) diopside-spinel dendritic lamella that probably originated due to the exsolution from high Ca- and Cr- primary magmatic olivine. All these features of Ol-1-C are typical of olivine from primitive picritic and komatiitic magmas (De Hoog et al., 2010; Asafov et al., 2018). Ol-1-C contains large (up to 0.25 mm) crystalline inclusions of high-Al enstatite (Mg# 80-88) and clinopyroxene (Mg# 82-90), occasionally in association with Ti-pargasite and chromian spinel (60.4 wt.% Al2O3). These inclusions are regarded as microxenoliths of wall rock that were captured by primary melt at depths more than 30 km and preserved due to the conservation in magmatic olivine. The second stage was responsible for the crystallization of Ol-1 rim (Ol-1-R), small (up to 0.3 mm) olivine (Ol-2, Mg# 76-85) grains, and central parts of large (up to 1.5 mm) clinopyroxene (Cpx-C) phenocrysts in the mid-crustal transitional magma chamber (at a depth of 15-20 km) at 1160-1350°C. At the third stage, Cpx-C phenocrysts were overgrown by low-Mg rims (Mg# 70-72) similar in composition to the groundmass clinopyroxene from chilled picrodolerite and gabbro-dolerite in the central parts of the sills. This stage likely completed the evolution of picrodoleritic magma and occurred in the upper crust at a depth of about 5 km. All stages of picrodoleritic magma crystallization were accompanied by contamination. Primary melts were contaminated by upper mantle and/or lower crust as recognized from xenocrystic inclusions in Ol-1-C. The second contamination stage is supported by the negative values of ?Nd(2.40) = -1.1 in clinopyroxene phenocrysts. At the third stage, contamination likely occurred in the upper crust when ascending melts filled gentle fractures. This caused vertical whole-rock Nd heterogeneity in the sills (Erofeeva et al., 2019), and difference in Nd isotopic composition of clinopyroxene phenocrysts and doleritic groundmass. It was also recognized that residual evolved melts are enriched in radiogenic strontium but have neodymium isotopic composition similar to other samples. It could be explained by the interaction of the melts with fluid formed via decomposition of biotite from surrounding gneisses under the effect of high-temperature melts.
Abstract: To provide new insights into the type and extent of mantle metasomatism in the subcratonic lithospheric mantle, we examined the Sr-Nd-O isotopic compositions of orthopyroxene, clinopyroxene, garnet, ilmenite and phlogopite from sheared garnet lherzolite, granular garnet harzburgites and lherzolites and clinopyroxene-phlogopite rocks from the Grib kimberlite in the Arkhangelsk diamond province in northwestern Russia. Clinopyroxene and orthopyroxene from sheared garnet lherzolite initially have a close value of 87Sr/86Sr(t) (~0.7034) and close weak positive ?Nd. Orthopyroxene and clinopyroxene are in oxygen isotope equilibrium with coexisting olivine. Clinopyroxene from a garnet harzburgite has a low 87Sr/86Sr(t) isotope ratio of 0.70266. Clinopyroxene from granular garnet lherzolites has a relatively narrow variation in 87Sr/86Sr(t) (0.70456-0.70582) and considerably larger variations in ?Nd (?4.3???+1.0) isotope ratios. Garnet displays elevated initial 87Sr/86Sr(t) values (0.70540-0.70633). Ilmenite shows a narrow range in 87Sr/86Sr(t) (0.70497-0.70522) coupled with ?Nd values of +0.4 and +3.5. These isotopic data suggest granular garnet lherzolite of mantle metasomatism took place during the interaction of kimberlite melts with SCLM that contained mica-amphibole-rutile-ilmenite-diopside (MARID)-type metasomes. Clinopyroxenes from clinopyroxene-phlogopite (phlogopite wehrlite) xenoliths display a broader range in 87Sr/86Sr(t) (0.70486-0.70813) that is significantly higher than the kimberlite values and a circa-chondritic ?Nd (?0.1 ??+1.3) with a restricted ?18O range (5.11‰-5.33‰). More radiogenic Sr isotopic composition decoupled from Nd isotopes could have been induced by metasomatic melt/fluid related to a subducted material. The isotopic compositions of mantle minerals preserve Sr-Nd isotopic evidence of pre-kimberlite metasomatic events that were probably due to incomplete reequilibration with ultramafic carbonated melt. Based on mineral pairs Rb-Sr isochrons and a clinopyroxene-based Sm-Nd errochron, these mantle metasomatic events correspond to ~550-600?Ma and ~1200?Ma episodes of magmatic-thermal activity.
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 ? = 1.604(2) and ? = 1.607(2) (? = 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) (?forumla?), 2.855 (100) (404). Sergevanite is named after the Sergevan' River, which is near the discovery locality.
Geology of Ore Deposits, Vol. 62, 8, pp. 754-763. pdf
Russia, Kola Peninsula
REE
Abstract: This paper presents the results of the first geological, isotope, geochemical, and mineralogical study of carbonatite veins that were previously unknown in the Soustov pluton. The studied veins are similar in the Sm-Nd isotope composition and model age to the host rocks, which implies a common formation processs. High contents of light lanthanides, Sr, and Nb in carbonatite veins were measured. These elements are concentrated in bastnäsite, strontianite, monazite, and pyrochlore. These data significantly enlarge our concepts of the geochemical and ore specialization of the massif.
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 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 ?REE + 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
Abstract: The study reports petrography, bulk major and trace element compositions of lamprophyric Devonian dykes in three areas of the Kola Alkaline Carbonatite Province (N Europe). Dykes in one of these areas, Kandalaksha, are not associated with a massif, while dykes in Kandaguba and Turij Mys occur adjacent (< 5 km) to coeval central multiphase ultramafic alkaline?carbonatitic massifs. Kandalaksha dyke series consists of aillikites - phlogopite carbonatites and monchiquites. Kandaguba dykes range from monchiquites to nephelinites and phonolites; Turij Mys dykes represent alnöites, monchiquites, foidites, turjaites and carbonatites. Some dykes show extreme mineralogical and textural heterogeneity and layering we ascribe to fluid separation and crystal cumulation. Melt evolution of the dykes was modelled with Rhyolite-MELTS and compared with the observed order and products of the crystallization. Our results suggest that the studied rocks were related by fractional crystallization and liquid immiscibility. Primitive melts of aillikites or olivine melanephelinites initially evolved at P = 1.5-0.8 GPa without a SiO2 increase due to abundant clinopyroxene crystallization controlled by the CO2-rich fluid. At 1-1.1 GPa the Turij Mys melts separated immiscible carbonatite melt, which subsequently exsolved late carbonate-rich fluids extremely rich in trace elements. Kandaguba and Turij Mys melts continued to fractionate at lower pressures in the presence of hydrous fluid to the more evolved nephelinite and phonolite melts. The studied dykes highlight the critical role of the parent magma chamber in crystal fractionation and magma diversification. The Kandalaksha dykes may represent a carbonatite - ultramafic lamprophyre association, which fractionated at 45-20 km in narrow dykes on ascent to the surface and could not get more evolved than monchiquite. In contrast, connections of Kandaguba and Turij Mys dykes to their massif magma chambers ensured the sufficient time for fractionation, ascent and a polybaric evolution. This longevity generated more evolved rock types with the higher alkalinity and an immiscible separation of carbonatites.
Abstract: 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 R3¯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.
Abstract: New results are presented on the features of the deep velocity structure of two of the three main tectonic blocks that make up the Kola region-Murmansk and Belomorskii-by the P receiver function technique. The research is based on data from the broadband seismic stations Teriberka and Kovda. The results are compared with the models obtained by mutual inversion of PRF and SRF using the data from the stations Apatity and Lovozero. It is shown that the crust has a two-layer structure with the border at a depth of 11 km under the Murmansk block and at a depth of 15 km under the Kola and Belomorskii blocks. The crust thickness of the Murmansk, Belomorskii, and Kola blocks are 35, 33, and 40 km, respectively. The presence of the MLD was revealed in all tectonic structures analyzed for the first time, with a top at a depth of about 70 km for the Murmansk and Belomorskii blocks and 90 km for the Kola block and a bottom at 130-140 km for all structures.
Abstract: Diamond crystals from the M.V. Lomonosov deposit (Archangelsk oblast, Russia) were studied by luminescence and infrared spectroscopy. Three groups of crystals were distinguished according to their morphology, thermal history, and photoluminescence. The structural diversity of yellow cuboids typical for the deposit is demonstrated. New photoluminescence systems among the low-temperature cuboid crystals are observed.