Pegmatites of Southern California

For many years the southern California region has attracted the attention of geologists interested in pegmatites and pegmatite deposits, largely because of the well-known gem and lithium occurrences in San Diego and Riverside Counties. These world-famous pegmatites have been so often noted or described in the literature that they commonly are regarded as typical of the pegmatites in the region, even though this actually is far from the case. More than 90 percent of all published contributions on California pegmatites deal with the gem-bearing dikes of San Diego County alone! It is the main purpose of this brief paper to summarize the distribution, occurrence, composition, and structure of all the known pegmatites in southern California, and to discuss several aspects of their geologic and economic significance. Much of the information has been obtained from the published record, a sampling of which is included in the list of references at the end of the paper. In larger part, however, the writer has found it necessary to draw from the results of his own observations, many of which were made in reconnaissance and hence are not wholly satisfactory as a background for generalizations. This qualification with respect to basic data plainly underlies the summary and discussions that follow

Minerals in Afghanistan : rare-metal deposits

In Afghanistan rare metals (lithium, caesium, tantalum and niobium) occur in three main deposit types: pegmatites, mineralised springs and playa-lake sediments (Figure 1). The most potentially significant, easily extractable resources of rare metals in Afghanistan occur in mineralised springs and playas, although there is also considerable potential for exploiting hard-rock pegmatite deposits. Globally, rare metals are produced from deposits in these three settings, chiefly in Chile, Argentina, the USA and Turkey. Lithium has many uses, for example in batteries, in the glass and ceramics industry, and in high performance alloys for aircraft. Most tantalum is used to produce capacitors that are used in laptop computers, mobile phones and digital cameras. Niobium is primarily used in specialist steels although it also shares some uses with tantalum since it has almost identical chemical properties

Diffusion-controlled and replacement microtextures in alkali feldspars from two pegmatites: Perth, Ontario and Keystone, South Dakota

Macro- and micro-perthitic microclines from pegmatites from Perth, Ontario (Wards catalogue 46 E 0510) and Keystone, South Dakota (Wards 46 E 5125) have been studied using light and electron microscopy. A sample of the type perthite from Perth, Ontario (Hunterian Museum, Glasgow, M2361) was compared using light microscopy. It differs in bulk composition and microtexture from the Wards sample. The Perth sample from Wards is a mesoperthite, with sub-periodic ~mm-thick albite veins near (100), with irregular surfaces. The microcline has regular tartan twins and formed from orthoclase by a continuous process. The Keystone sample is a microperthite, with non-periodic albite veins mainly in {110}. Irregular tartan twins, volumes of irregular microcline and subgrains suggest that the microcline formed by dissolution–reprecipitation. Microcline in both samples contains semicoherent cryptoperthitic albite films that formed after the development of tartan twins. The bulk compositions of these intergrowths imply exsolution below ~400°C. Diffusion parameters imply sustained heating for between 0.11 My at 400°C, 1.5 GPa and 8.4 My at 300°C, 1 GPa. Unrealistic times are required at 200°C. Subsequently, the crystals reacted with a fluid leading to replacive growth of the vein perthites. Unusually, Albite twin composition planes in replacive subgrains have sub-periodic dislocations, formed by coalescence of advancing growth twins. Processes that might lead to periodic, replacive intergrowths are discussed. The Perth and Keystone feldspars have been used for experimental work on dissolution during weathering and on anomalous thermoluminescence fading. Their microtextures make them unsuitable for obtaining properties that can be extrapolated to feldspars in general

Internal framework and geochemistry of the Carboniferous Huaco granite pluton, Sierra de Velasco, NW Argentina

The A-type Huaco granite pluton of the Velasco range (Sierras Pampeanas of northwest Argentina) is formed by three coeval granitic facies and contains subordinate coeval-to-late facies, as well as enclaves, dikes and stocks that show different temporal relations, textures and compositions. The dominant facies (Regional Porphyritic Granite; RPG) is a porphyritic two-mica monzo- to syenogranite, with abundant microcline megacrysts up to 12 cm in size. It was emplaced in a dominant extensional setting and has a mainly crustal source but with participation of a mantle-derived component. The RPG transitions towards two coeval and co-genetic granite facies, at its margins (Border Granite; BG) and around Be-pegmatites (Adjacent Porphyritic Granite; APG). These two facies have a finer-grained texture and smaller and less abundant megacrysts. They are also monzo- to syenogranites, but a slight decrease in the biotite/muscovite ratio is observed from the BG to the RPG to the APG. Trace element modeling suggests that the RPG, BG and APG differentiated from the same magma source by fractional crystallization. Temporally older mafic (ME) and felsic (FE) enclaves are common in the pluton. The ME can be considered partially assimilated remnants of a mafic component in the genesis of the RPG, whereas the FE seem to be remnants of premature aplites. Other subordinate rocks intrude the RPG and are, hence, temporally younger: felsic dikes (FD), dioritic dikes (DD) and equiganular granites (EqG) are clearly posterior, whereas coeval-to-late Be-pegmatites (BeP) and orbicular granites (OG) formed during the final stages of crystallization of the pluton. The BeP, OG and FD indicate the presence of abundant water and volatiles. The EqG form small stocks that intrude the RPG and were possibly originated from purely crustal sources. The DD probably correspond to a younger unrelated episode of mafic magmatism.Fil: Sardi, Fernando Guillermo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto Superior de Correlación Geológica. Universidad Nacional de Tucumán. Facultad de Ciencias Naturales e Instituto Miguel Lillo. Departamento de Geología. Cátedra Geología Estructural. Instituto Superior de Correlación Geológica; ArgentinaFil: Grosse, Pablo. Fundación Miguel Lillo. Dirección de Geología. Instituto de Minerología y Petrografia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; ArgentinaFil: Murata, Mamoru. Naruto University; JapónFil: Lozano Fernández, Rafael Pablo. Instituto Geológico y Minero de España; Españ

Typomorphism of perthitic intergrowth of feldspars from granitic pegmatites from the area of west Azov (Ukrainian shield)

Приведены данные о вещественном составе графических пегматитов с различной специализацией кварца и отмечено широкое развитие пертитовых вростков в полевых шпатах. Проанализированы типоморфные признаки пертитов и антипертитов и их генетическая информативность. Предложен вероятный механизм образования данных пород.Наведено дані про речовинний склад графічних пегматитів з різною спеціалізацією кварцю і відмічено значне поширення пертитових зрощень у польових шпатах. Проаналізовано типоморфні ознаки пертитів та антіпертитів та їх генетична інформативність. Запропоновано ймовірний механізм утворення даних порідThe results of material composition of graphic pegmatite quartz with different specialization and noted the broad development perthitic intergrowths in feldspars. Analyses are given of typomorphic signs perthites and antiperthites and their genetic information content. We propose a probable mechanism of formation of these rocks

Geochemical Characterization of Mineralized Pegmatites around Wowyen Areas, Akwanga, Northcentral Nigeria

This study aims to account for the petrogenesis and mineralization of pegmatites around the Wowyen area, northcentral basement complex,Nigeria. Field studies, petrography and whole rock geochemistry (Major oxides were estimated by X-Ray Fluorescence while the trace elements were estimated by Inductively Coupled Plasma Mass Spectrometry) where the methods adopted. The pegmatites around Wowyen area are emplaced in the remobilized belt of the Nigerian Basement complex. They are predominantly complex pegmatites (rare-metal pegmatites) which are intruded in the biotite-muscovite gneiss while the simple pegmatites intruded more in the migmatitic banded gneiss. The major components of the complex pegmatites are quartz, albite and muscovite and tourmaline.The accessory constituents are garnet; ilmenites; cassiterite-columbitetantalite oxides in contrast to quartz, microcline and biotite of the simple pegmatites. The complex pegmatites show higher peraluminous than the simple pegmatites, however, higher fractionation is observed in the complex pegmatites than the simple pegmatites. The complex pegmatites are rather enriched in rare elements such as Li, Rb, B, Cs, Sn, Nb, Be and Ta and show low ratios in Al/Ga and K/Rb than the simple pegmatites. The pegmatites are likely product of sedimentary origin and originated from post-collisional tectonic event

Late Precambrian U-Pb titanite age for peak regional metamorphism and deformation (Knoydartian orogeny) in the western Moine, Scotland

There has been controversy over the number and timing of orogenies in the Precambrian Moine block in the Scottish Caledonides since the earliest radiometric dating in the 1960s. This work challenges a recent hypothesis, that this sector of the Laurentian margin was subjected to continuous crustal extension between greater than 900 and 470 Ma. U-Pb dating (thermal ionization mass spectrometry) of titanite from a calcsilicate pod in the Moine (Morar Group) of the western Highlands gives an age of 737 ñ 5 Ma. The titanite grew from Fe-Ti-bearing detrital minerals during the main progressive, syn-D2, amphibolite-facies (sillimanite zone) regional metamorphism, thus demonstrating that a Neoproterozoic contractional tectonothermal event (Knoydartian orogeny) affected the Moine block following the rift-related emplacement of the West Highland granite gneiss at 873 Ma. We conclude that the Sgurr Beag Thrust, a major tectonic break separating the Morar and Glenfinnan groups of the Moine, is mainly of Neoproterozoic, not Caledonian, age. The early tectonothermal event was succeeded by the Grampian Phase (Caledonian orogeny) at 460-470 Ma

Metamorphic and metasomatic evolution of the Western Domain of the Karagwe-Ankole Belt (Central Africa)

The tectonometamorphic evolution of the Western Domain of the Karagwe-Ankole Belt, containing widespread granite-related W-Nb-Ta-Sn mineralization in pegmatites and hydrothermal quartz veins of Early Neoproterozoic age, is largely unknown. This study aims to characterize the Meso- and Neoproterozoic metamorphism and metasomatism in the Karagwe-Ankole Belt, to reconstruct the temperature evolution and to investigate its temporal relation to deformation and the widespread granite magmatism and mineralization. A quantitative geothermometric study was conducted on metasiltstones and amphibolites, and applies thin section petrography, garnet-biotite and chlorite geothermometry on samples collected in the representative KibuyeGitarama-Gatumba area in West Rwanda. The presence of garnet, staurolite and kyanite in metasiltstones, and hornblende and andesine-labradorite feldspar in amphibolites indicates prograde Barrovian metamorphism up to syn-to post-deformational (D1 or D2) lower amphibolite facies (up to 630 degrees C). This peak metamorphism was followed by post-D2 greenschist facies metamorphism (c. 525 degrees C-440 degrees C; garnet, biotite, chlorite, muscovite in metasiltstone), probably related to the East African Orogeny as part of the Gondwana assembly. A geothermometric evolution with high temperature conditions ( > 500 degrees C) at least from the flare-up of Early Neoproterozoic tin granites and their metasomatic haloes onwards for most of the Neoproterozoic is proposed, in close correspondence with the geodynamic evolution of the neighboring terranes. Additionally, this high temperature regime is an important factor to be taken into account when interpreting thermal diffusion-sensitive geochronological data

Carlhintzeite, Ca2AlF7•H2O, from the Gigante granitic pegmatite, Córdoba province, Argentina: Description and crystal structure

Carlhintzeite, Ca2AlF7•H2O, has been found at the Gigante pegmatite, Punilla Department, Córdoba Province, Argentina. It occurs as colourless prismatic crystals up to 0.8 mm long, ubiquitously twinned on {001}. Electron microprobe analyses provided the empirical formula Ca1.98Al1.02F6.24(OH) 0.76•H1.62O. A crystal fragment used for the collection of structure data provided the triclinic, C1 cell: a = 9.4227(4), b = 6.9670(5), c = 9.2671(7) Å, α = 90.974(6), β = 104.802(5), γ = 90.026(6)°, V = 558.08(7) Å3 and Z = 4. The crystal structure, solved by direct methods and refined to R 1 = 0.0322 for 723 Fo > 4σF reflections, is made up of linkages of AlF6 octahedra, CaF8 polyhedra and CaF 6(H2O)2 polyhedra. The AlF6 octahedra are isolated from one another, but share polyhedral elements with Ca polyhedra. Most notably, the Al1 octahedron shares trans faces with two CaF 8 polyhedra and the Al2 octahedron shares trans edges with two CaF6(H2O)2 polyhedra. The linkage of the Ca polyhedra alone can be described as a framework in which edge-sharing chains along b are cross-linked by edge-sharing. Edge-sharing chains of Ca polyhedra along b in the carlhintzeite structure are similar to those along c in the structures of gearksutite, CaAlF4(OH)•(H2O), and prosopite, CaAl2F4(OH)4. © 2010 Mineralogical Society.Fil: Kampf, A. R.. Natural History Museum of Los Angeles County; Estados UnidosFil: Colombo, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Ciencias de la Tierra. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Centro de Investigaciones en Ciencias de la Tierra; ArgentinaFil: González Del Tánago, J.. Universidad Complutense de Madrid; Españ

A partial molar volume for B 2 O 3 in haplogranitic melt

The densitiesa nd thermal expansivitieso f boron-bearingh aplogranitic glassesa nd Iiquids have been determined using a combination of scanning .florimetry and dilatomelry. B2O3 reduces the density of haplogranitic liquids (at 750'C) from 2.295 t 0.006 g cm-r to 2.237 + 0.005 g cm-3 wirh the addition of 8.92 wt. Vo 82o,. These densities have been converted into molar volumes in the binary system haplogranite - BrO3. The partial molar volume of 8203, calculated from a linear fit to the data at 750oC, is ,10.30 + 0.77 cmr mole-r in these melts. This value compares with a molar volume of pure B2O3 at this temperature of M.36 x. 0.22 cm3 mole-l (Napolitano et ol. 1965), indicating a negative excess volume of mixing along the haplogranite - B2O3 join. In comparison, at l3moc, the addition ot Na2O to B2O3 reduces the panial molar volume of B2O3 from 46.6 to 32.3 cm3 mole-r ar 45 molego Na2O (Riebling 1966).T he densityr esultsr eported here, along with the viscosity-reducinge ffect of B2O3o n granitic melts (Dingwell et al, 1992),s hould both significantlya cceleratep rocesseso f crystal-melt fractionation and facilitate the evolution of extremely fractionated igneous systems