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The Sheahan Diamond Literature Reference Compilation - Technical Articles based on Major Region - Urals
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 ŕ 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]
The Applications of Geology to the Arts and Manufacturers. Being Six Lectures on Practical Geology, Delivered Before The Society of Arts, As a Part of the Cantor Series of Lectures for 1865.
Sources of Diamonds of Urals Placers in Connection with The article by Stepanov and Sychkin Entitled Estimating the Degree of Reliability of Some Diamond Finds.
Soviet Geology And Geophysics, Vol. 21, No. 9, PP. 140-143.
high pressure metamorphic rocks of a new type: the lherzolite-gabbro-granulite series in the base of the ultramafic section in the Voykar ophiolite allochthon Polar
Doklady Academy of Sciences USSR, Earth Science Section, Vol. 318, No. 6, pp. 148-153.
Russia, Commonwealth of Independent States (CIS), Polar Urals
Comparative charcteristics of specific morphological features of diamonds from northern and northeastern European Russia ( Urals, Timan, and Arkhangelsk).
Moscow University Geology Bulletin, Vol. 56, 6, pp. 26-30.
Prospects of bedrock diamond bearing capacity of the conjugation zone between the Sysolsky anticline and Kirovsk-Kazhimsk aulocogen north of Volga-Urals anteclise.
Doklady Earth Sciences, Vol. 423A, No. 9, pp. 1348-1351.
Origin and evolution of the Ilmeny-Vishnevogorsky carbonatites ( Urals, Russia): insights from trace element compositions, and Rb Sr Sm Nd, U Pb, Lu Hf isotope data.
Mineralogy and Petrology, Vol. 107, 1, pp. 101-123.
Trace element and isotopes Hf as a signature of zircon genesis during evolution of alkaline carbonatite magmatic system ( Ilmeny Vishnevogorsky complex, urals, Russia.)
30th. International Conference on Ore Potential of alkaline, kimberlite and carbonatite magmatism. Sept. 29-, http://alkaline2014.com
Mineralogy and Petrology, Vol. 109, 2, pp. 143-152.
Russia, Urals
Mineralogy
Abstract: A new picromerite-group mineral, nickelpicromerite, K2Ni(SO4)2 - 6H2O (IMA 2012-053), was found at the Vein #169 of the Ufaley quartz deposit, near the town of Slyudorudnik, Kyshtym District, Chelyabinsk area, South Urals, Russia. It is a supergene mineral that occurs, with gypsum and goethite, in the fractures of slightly weathered actinolite-talc schist containing partially vermiculitized biotite and partially altered sulfides: pyrrhotite, pentlandite, millerite, pyrite and marcasite. Nickelpicromerite forms equant to short prismatic or tabular crystals up to 0.07 mm in size and anhedral grains up to 0.5 mm across, their clusters or crusts up to 1 mm. Nickelpicromerite is light greenish blue. Lustre is vitreous. Mohs hardness is 2-2˝. Cleavage is distinct, parallel to {10-2}. Dmeas is 2.20(2), Dcalc is 2.22 g cm?3. Nickelpicromerite is optically biaxial (+), ? = 1.486(2), ? = 1.489(2), ? = 1.494(2), 2Vmeas =75(10)°, 2Vcalc =76°. The chemical composition (wt.%, electron-microprobe data) is: K2O 20.93, MgO 0.38, FeO 0.07, NiO 16.76, SO3 37.20, H2O (calc.) 24.66, total 100.00. The empirical formula, calculated based on 14 O, is: K1.93Mg0.04Ni0.98S2.02O8.05(H2O)5.95. Nickelpicromerite is monoclinic, P21/c, a = 6.1310(7), b = 12.1863(14), c = 9.0076(10) Ĺ, ? = 105.045(2)°, V = 649.9(1) Ĺ3, Z = 2. Eight strongest reflections of the powder XRD pattern are [d,Ĺ-I(hkl)]: 5.386--34(110); 4.312-46(002); 4.240-33(120); 4.085--100(012, 10-2); 3.685-85(031), 3.041-45(040, 112), 2.808-31(013, 20-2, 122), 2.368-34(13-3, 21-3, 033). Nickelpicromerite (single-crystal X-ray data, R = 0.028) is isostructural to other picromerite-group minerals and synthetic Tutton’s salts. Its crystal structure consists of [Ni(H2O)6]2+ octahedra linked to (SO4)2? tetrahedra via hydrogen bonds. K+ cations are coordinated by eight anions. Nickelpicromerite is the product of alteration of primary sulfide minerals and the reaction of the acid Ni-sulfate solutions with biotite.
Hf isotopes and trace elements as indicators of zircon genesis in the evolution of the alkaline-carbonatite magmatic system ( Il'meno-Visnevogorskii complex, Urals, Russia.)
Yang, J.S., Wirth, R., Wiedenbeck, M., Griffin, W.L., Meng, F.C., Chen, S.Y., Bai, W.J., Xu, X.X., Makeeyev, A.B., Bryanchaniniova, N.I.
Diamonds and highly reduced minerals from chromitite of the Ray-Iz ophiolite of the Polar Urals: deep origin of podiform chromitites and ophiolitic diamonds.
Abstract: Two areas with different types of hydration (serpentinization), which occurred in two settings distinct in temperatures, pressures, and stresses, are spatially individualized in the ophiolitic ultramafic massifs of the Polar Urals. The high-temperature hydration of ultramafic rocks occurred in the lithosphere of the mantle wedge directly above the subducted slab. The initial conditions of hydration are limited to 1.2-2 GPa and 650-700°C; a stable assemblage of olivine + antigorite + magnetite ? amphibole ? talc ? chlorite was formed at 0.9-1.2 GPa and 550-600°C. The low-temperature mesh lizardite-chrysotile serpentinization occurred in the crustal, near-surface conditions. Both types of hydration were accompanied by release of hydrogen, which participates in abiogenic CH4 synthesis in the presence of CO2 dissolved in water.
Abstract: Microdiamonds ?200 ?m in size, occurring in ophiolitic chromitites and peridotites, have been reported in recent years. Owing to their unusual geological formation, there are several debates about their origin. We studied 30 microdiamonds from 3 sources: (1) chromitite ore in Luobusa, Tibet; (2) peridotite in Luobusa, Tibet; and (3) chromitite ore in Ray-Iz, polar Ural Mountains, Russia. They are translucent, yellow to greenish-yellow diamonds with a cubo-octahedral polycrystalline or single crystal with partial cubo-octahedral form. Infrared (IR) spectra revealed that these diamonds are type Ib (i.e., diamonds containing neutrally charged single substitutional nitrogen atoms, Ns0, known as the C center) with unknown broad bands observed in the one-phonon region. They contain fluid inclusions, such as water, carbonates, silicates, hydrocarbons, and solid CO2. We also identified additional microinclusions, such as chromite, magnetite, feldspar (albite), moissanite, hematite, and magnesiochromite, using a Raman microscope. Photoluminescence (PL) spectra measured at liquid nitrogen temperature suggest that these diamonds contain nitrogen-vacancy, nickel, and H2 center defects. We compare them with high-pressure-high-temperature (HPHT) synthetic industrial diamond grits. Although there are similarities between microdiamonds and HPHT synthetic diamonds, major differences in the IR, Raman, and PL spectra confirm that these microdiamonds are of natural origin. Spectral characteristics suggest that their geological formation is different but unique compared to that of natural gem-quality diamonds. Although these microdiamonds are not commercially important, they are geologically important in that they provide an understanding of a new diamond genesis.
Abstract: A wide range of model temperature, which is typical for dodecahedroids from placer deposits in the Urals, Brazil, and the northern Yakutia diamond province has been identified in diamond crystals of the Ichetyu Ural-type diamonds deposit, Central Urals. Plates were cut from six crystals; it have been studied with cathodoluminescence and infrared and photoluminescence spectroscopy. Octahedral zoning predominates in the internal structure of rounded dodecahedroids, and growth layers are cut by the surface. Surface pigmentation spots are exhibited in the cathodoluminescent images of all plates. The nitrogen concentration in Ichetyu diamonds ranges from 100 to 2200 ppm and its proportion as B1 defects varies from 0 to 100%. The maximum absorption coefficient of hydrogen band is 56 cm-1 with an average value of 0.8 cm-1.
Abstract: The first data on the discovery of Th-Sc mineralization in the pyritic complexes of the Southern Urals are presented. The minerals of Th (thorite) and Sc-containing thorium minerals are described. The conclusion is made that the Th-Sc mineralization formed due to crystallization of a residual melt in the local volume.
Abstract: We have investigated a diamond crystal that consists of several misorientated subgrains. The main feature of the crystal is the dark in the cathodoluminescence core that has “estuary-like” boundaries extending along the subgrain interfaces. The core has more than 3100 ppm of nitrogen, and the share of the B form is more than 95%; the absorbance of the centre N3VH at 3107 cm -1 reaches 75 cm-1. The N3 centre’s absorbance, as well as N3 luminescence, is absent in the core. In the outer part of the crystal, the bright blue luminescence of the N3 centre is registered, and the N3 absorbance reaches 5.3 cm-1. These observations may be explained by the conversion of N3 centres to N3VH after attaching a hydrogen atom. After the full conversion of the N3 centres, the diamond becomes darker under CL. We hypothesize the dark core has a specific shape due to the post-growth diffusion of the hydrogen.
Geochimica et Cosmochimica Acta, Vol. 266, pp. 197-212.
Russia, Urals
diamond inclusions
Abstract: The compositions of mineral inclusions from a representative collection (more than 140 samples) of diamonds from the placer deposits in the Ural Mountains were studied to examine their compositional diversity. The overwhelming majority of rounded octahedral and dodecahedral stones typical of placers contain eclogitic (E-type) mineral inclusions (up to 80%) represented by garnets with Mg# 40-75 and Ca# 10-56, including the unique high calcic “grospydite” composition, omphacitic pyroxenes containing up to 65% of jadeite, as well as kyanite, coesite, sulfides, and rutile. Peridotitic (P-type) inclusions are represented by olivine, subcalcic Cr-pyrope, chrome diopside, enstatite and magnesiochromite that are typical for diamonds worldwide. Comparing the chemical composition of olivine, pyrope and magnesiochromite in diamonds of the Urals, north-east of the Siberian platform placers and Arkhangelsk province kimberlites show striking similarity. There are significant differences only in the variations of carbon isotopic composition of the diamonds from the placers of the Urals and north-east of the Siberian platform. One typical rounded dodecahedral diamond was found to contain abundant primary oriented submicrometer-sized (<3.0?µm) octahedral fluid inclusions identified by transmission electron microscopy, which caused the milky color of the entire diamond crystal. The electron energy-loss spectrum of a singular inclusion has a peak at ?405?eV, indicating that nitrogen is present. The Raman spectra with peaks at 2346-2350?cm?1 confirmed that nitrogen exists in the solid state at room temperature. This means that fossilized pressure inside fluid inclusions may be over 6.0 GPa at room temperature, so the diamond may be considered sublithospheric in origin. However, identification of unique fluid inclusions in one typical placer diamond allows one to expand the pressure limit to at least more than 8.0 GPa. The volatile components of four diamonds from the Urals placers were analyzed by gas chromatography-mass spectrometry (GC-MS). They are represented (rel. %) by hydrocarbons and their derivatives (14.8-78.4), nitrogen and nitrogenated compounds (6.2-81.7), water (2.5-5.5), carbon dioxide (2.8-12.1), and sulfonated compounds (0.01-0.96). It is shown that high-molecular-weight hydrocarbons and their derivatives, including chlorinated, nitrogenated and sulfonated compounds, appear to be stable under upper mantle P-T conditions. A conclusion is drawn that Urals placer diamonds are of kimberlitic origin and are comparable in their high E-type/P-type inclusion ratios to those from the northeastern Siberian platform and in part to diamonds of the Arkhangelsk kimberlite province.
Geology of Ore Deposits, Vol. 61, 7, pp. 598-605. pdf
Russia, Urals
diamond morphology
Abstract: Three hundred thirty-six diamonds from deposits of the Rassolninskaya depression and 144 crystals from recent alluvial placers of the Krasnovishersky district were studied by IR absorption and photoluminescence spectroscopy. It is shown that crystals from the Rassolninskaya depression have a close-to-normal distribution for the nitrogen concentration. The average nitrogen content is 725 ppm, and no nitrogen-free crystals were detected. A sampling from recent alluvial placers contains 25% crystals with a nitrogen concentration smaller than 150 ppm; 3% of them are nitrogen-free. Among crystals from the Rassolninskaya depression, 12% are octahedral, 80% rhombododecahedral, and only one crystal has relicts of cubic faces. The collection from recent placers contains 3% cubic crystals, 10% individuals with relicts of cubic faces, 16% octahedroids, and 66% dodecahedra. Alluvial diamonds are often encountered with crescent-shaped cracks; however, they were observed only on a single crystal from the Rassolninskaya depression. It has been revealed that among alluvial placer diamonds, up to 95% of crystals contain nitrogen in the form of B1 defects. Thus, first, in morphological and structural-mineralogical features, diamonds from the Rassolninskaya depression differ from crystals of the nearest recent alluvial placers; second, they may belong to primary deposits based on the set of their characteristics.
Abstract: Mineral zoning in fenites around miaskite intrusions of the Vishnevye Mountains complex can be interpreted as a magmatic-replacement zonal metasomatic aureole (in D.S. Korzhinskii’s understanding): the metasomatic transformations of the fenitized gneisses under the effect of deep alkaline fluid eventually resulted in the derivation of nepheline syenite eutectic melt. Based on the P-T-fO2 parameters calculated from the composition of minerals coexisting in the successive zones, isobaric-isothermal fO2-aSiO2 and µNa2O-µAl2O3 sections were constructed with the Perplex program package to model how the fenites interacted with H2O-CO2 fluid (in the Na-K-Al-Si-Ca-Ti-Fe-Mg-O-H-C system). The results indicate that the fluid-rock interaction mechanisms are different in the outer (fenite) and inner (migmatite) parts of the zonal aureole. Its outer portion was dominated by desilication of rocks, which led, first, to quartz disappearance from these rocks and then to an increase in the Al# of the coexisting minerals (biotite and clinopyroxene). In the inner part of the aureole, fenite transformations into biotite-feldspathic metasomatic rocks and nepheline migmatite were triggered by an increase in the Na and Al activities in the system alkaline H2O-CO2 fluid-rock. As a consequence, the metasomatites were progressively enriched in Al2O3 and alkalis, and these transformations led to the development of biotite in equilibrium with K-Na feldspar and calcite at the sacrifice of pyroxene. The further introduction of alkalis led to the melting of the biotite-feldspathic metasomatites and the origin of nepheline migmatites. The simulated model sequence of metasomatic zones that developed when the gneiss was fenitized and geochemical features of the successive zones (differences in the LILE and REE concentrations in the rocks and minerals of the fenitization aureole and the Sm-Nd isotope systematics of the rocks of the alkaline complex) indicate that the source of the fluid responsible for the origin of zonal fenite-miaskite complexes may have been carbonatite, a derivative of mantle magmas, whereas the miaskites were produced by metasomatic transformations of gneisses and subsequent melting under the effect of fluid derived from carbonatite magmas.
Abstract: Mineral zoning in fenites around miaskite intrusions of the Vishnevye Mountains complex can be interpreted as a magmatic-replacement zonal metasomatic aureole (in D.S. Korzhinskii’s understanding): the metasomatic transformations of the fenitized gneisses under the effect of deep alkaline fluid eventually resulted in the derivation of nepheline syenite eutectic melt. Based on the P-T-fO2 parameters calculated from the composition of minerals coexisting in the successive zones, isobaric-isothermal fO2-aSiO2 and µNa2O-µAl2O3 sections were constructed with the Perplex program package to model how the fenites interacted with H2O-CO2 fluid (in the Na-K-Al-Si-Ca-Ti-Fe-Mg-O-H-C system). The results indicate that the fluid-rock interaction mechanisms are different in the outer (fenite) and inner (migmatite) parts of the zonal aureole. Its outer portion was dominated by desilication of rocks, which led, first, to quartz disappearance from these rocks and then to an increase in the Al# of the coexisting minerals (biotite and clinopyroxene). In the inner part of the aureole, fenite transformations into biotite-feldspathic metasomatic rocks and nepheline migmatite were triggered by an increase in the Na and Al activities in the system alkaline H2O-CO2 fluid-rock. As a consequence, the metasomatites were progressively enriched in Al2O3 and alkalis, and these transformations led to the development of biotite in equilibrium with K-Na feldspar and calcite at the sacrifice of pyroxene. The further introduction of alkalis led to the melting of the biotite-feldspathic metasomatites and the origin of nepheline migmatites. The simulated model sequence of metasomatic zones that developed when the gneiss was fenitized and geochemical features of the successive zones (differences in the LILE and REE concentrations in the rocks and minerals of the fenitization aureole and the Sm-Nd isotope systematics of the rocks of the alkaline complex) indicate that the source of the fluid responsible for the origin of zonal fenite-miaskite complexes may have been carbonatite, a derivative of mantle magmas, whereas the miaskites were produced by metasomatic transformations of gneisses and subsequent melting under the effect of fluid derived from carbonatite magmas.
MDPI Crystals, Vol. 11, 17 dx.doi.org/ 103390/ Qcrystal11010017 24p. Pdf
Russia, Yakutia, Urals, South America, Brazil
deposits - Mir, Udachnaya, Aikal, Yubilenya
Abstract: Ballas diamond is a rare form of the polycrystalline radial aggregate of diamonds with diverse internal structures. The morphological features of ballas diamonds have experienced repeated revision. The need that this paper presents for development of a crystal-genetic classification was determined by a rich variety of combined and transitional forms of ballas-like diamonds, which include aggregates, crystals, and intergrowths. The new crystal-genetic classification combines already-known and new morphological types of ballas as well as ballas-like diamonds discovered in the placers of Yakutia, the Urals, and Brazil. The ballas-like diamond forms include spherocrystals, aggregates with a single crystal core, split crystals, radial multiple twin intergrowths, and globular crystals. The crystal genetic scheme of the evolution of ballas and ballas-like diamonds is a sequence of the morphological types arranged in accordance with the conventional model of the dependence of the mechanism and diamond growth from carbon supersaturation developed by I. Sunagawa. The evolution of the growth forms of ballas and ballas-like diamonds was tracked based on the macrozonal structure of diamonds varying from a flat-faced octahedron to a fibrous cuboid with its transition forms to the radiating crystal aggregates. The morphological diversity of the ballas-like diamonds depends on the level of supersaturation, and abrupt changes of the level of supersaturation engender abrupt changes in a mechanism of crystal growth. The change in the rate of growth under the influence of adsorption and absorption of the mechanic impurities accompanied the sudden appearance of the autodeformation defects in the form of splitting and multiple radial twinning of crystals. The spherical shape of Yakutia ballas-like diamonds is due to the volumetric dissolution that results in the curved-face crystals of the "Urals" or "Brazilian" type associated with ballas diamonds in placers.
Geology of Ore Deposits, Vol. 62, 8, pp. 743-753. pdf
Russia, Urals
cuboid diamonds
Abstract: The internal structure and spectroscopic features of cuboid diamonds from recent alluvial placers of the Krasnovishersk District (the Urals) have been investigated. Crystals were divided into four groups by their anatomy and spectroscopy: cuboids of the II group (according to the Yu.L. Orlov classification): cuboids with a transparent core and peripheral zone saturated with inclusions; crystals with mixed habit growth of ?100? and ?111? pyramids, and crystals with the sequential growth of ?100? and ?111? pyramids. In all studied crystals, the regenerative formation of the {111} face steps together with the formation of tetragonal pits on the cuboid surface was the last stage of growth. Local photoluminescence investigations have been carried out for all cubic diamond crystals of the Urals for the first time. It was established that luminescence bands at 926 and 933 nm are related to growth pyramids of ?100? and ?111?, respectively. Bands with peaks at 800, 820.5, 840, 860, and 869 nm were revealed in the luminescence systems of the cuboids of II group. We note that the cuboid diamonds from different regions of the world have similar internal structures and spectroscopic features.
