Phosphate mineral associations in the Cañada pegmatite (Salamanca, Spain) : Paragenetic relationships, chemical compositions, and implications for pegmatite evolution

2004 ◽  
Vol 89 (1) ◽  
pp. 110-125 ◽  
Author(s):  
Encarnación Roda ◽  
Alfonso Pesquera ◽  
François Fontan ◽  
Paul Keller
Author(s):  
Idoia Garate-Olave ◽  
Encarnación Roda-Robles ◽  
Pedro Pablo Gil-Crespo ◽  
Alfonso Pesquera

ABSTRACT In the Tres Arroyos granite-pegmatite system (Badajoz, Spain) a zoned aplite-pegmatite field occurs, with poorly evolved, intermediate, and Li-rich dikes intruded into metasediments, close to the contact with the Nisa-Alburquerque granitic batholith. A large variety of Fe-Mn phosphate minerals occur in the poorly evolved aplite-pegmatites; Al-phosphates occur mainly in the intermediate and Li-rich dikes. The Fe/(Fe + Mn) ratio of the Fe-Mn phosphates is the highest reported for aplite-pegmatite fields in the Central Iberian Zone, suggesting a low degree of fractionation for the poorly evolved aplite-pegmatites that host these minerals. In contrast, the high F contents observed in crystals of the amblygonite–montebrasite series from the intermediate and Li-rich aplite-pegmatites indicates a higher fractionation degree for these dikes. The relatively common occurrence of phosphate minerals in the three types of aplite-pegmatites from Tres Arroyos attests to a significant availability of P in the pegmatitic melt. In this granite pegmatite system, P first started behaving as a compatible element, thus favoring the crystallization of discrete phosphates, during the crystallization of the poorly evolved aplite-pegmatites. In more fractionated melts, where Fe-Mn-(Mg) contents were extremely depleted, P was still available, allowing the crystallization of the Al-phosphates, mainly of the amblygonite–montebrasite series, in the more evolved intermediate and Li-rich aplite-pegmatites. Subsolidus replacement of the early phosphate phases, such as those of the amblygonite–montebrasite series, by lacroixite, together with the presence of late Ca- and Sr-bearing phosphates such as jahnsite-(CaMnFe), whiteite-(CaFeMg), mitridatite, and goyazite, attest to a high activity of metasomatic fluids in the Tres Arroyos granite-pegmatite system. Consequently, variations in the phosphate mineral associations and in their chemical compositions reflect well the fractional crystallization processes suffered by the pegmatitic melts from the poorly evolved up to the Li-rich dikes, as well as the subsolidus history of the Tres Arroyos system.


Georesursy ◽  
2020 ◽  
Vol 22 (2) ◽  
pp. 56-66
Author(s):  
Sergey G. Kovalev ◽  
Andrey V. Maslov ◽  
Sergey S. Kovalev

The article provides new data on geochemistry and mineralogy of rare-earth elements (REE) in rocks of structural-material complexes of the Bashkir megaanticlinorium, which underwent metamorphic transformations of various nature: contact metamorphism (Suran section); syn- and postgenetic contact-dislocation metamorphism (Shatak complex) and hydrothermal metamorphism (Uluelga-Kudashmanovo zone). It has been established that when a magmatic melt is exposed to sediments, the latter are enriched with REEs with the formation of rare earth minerals (monazite, allanite, xenotime et al.). The study of the chemical composition of monazites and allanites showed that all variations of oxides in the composition of the former are due to isomorphous Ce-Ca-Th substitutions in the structure of minerals, but redistribution of these elements was an independent process characteristic of each structural-material complex. The study of allanites made it possible to establish the presence of isomorphism according to the Ca↔Ce, La, Nd principle, as well as the sharp difference between the characterized minerals in the amount of MgO, Fe* and MnO from analogues from other regions, which indicates the presence of a regional component in the chemical compositions of minerals altogether, geotectonic settings of mineralization formation. The temperature regimes of mineral-forming processes with metamorphic transformations of rocks calculated from chlorite and muscovite compositions (344-450°C – Suran section, 402-470°C – Shatak complex, 390-490°C – Uluelga-Kudashmanovo zone) indicate the possibility of stable coexistence of the association monazite-allanite. It was established that when a magmatic melt on the sedimentary substrate of the frame, the lanthanides enrich the exocontact rocks with the formation of newly formed REE-mineral associations. At the same time, the processes of formation of rare-earth mineralization are largely determined by the physicochemical parameters and thermobaric conditions of the accompanying and subsequent metamorphism.


Author(s):  
Igor V. Pekov ◽  
Irina A. Ekimenkova

NOTE: This article was published in a former series of GEUS Bulletin. Please use the original series name when citing this article, for example: Pekov, I. V., & Ekimenkova, I. A. (2001). Two new rare-earth-rich mineral associations in the Ilímaussaq alkaline complex, South Greenland. Geology of Greenland Survey Bulletin, 190, 143-144. https://doi.org/10.34194/ggub.v190.5185 _______________ Two new types of REE-rich mineral associations have been discovered at Kvanefjeld in the northern part of the Ilímaussaq alkaline complex. Type 1 consists of ussingite veins intersecting lujavrite and containing 5–7% nacareniobsite-(Ce) and 2–4% steenstrupine-(Ce); the adjacent altered lujavrite contains up to 10–12% nacareniobsite-(Ce). Type 2 consists of cavernous sodalite-rich veinlets and vugs in lujavrite containing 5–8% vitusite-(Ce). The chemical compositions and unit cell parameters of REE minerals are given. Nacareniobsite-(Ce) and vitusite-(Ce) were considered to be extremely rare minerals in the Ilímaussaq complex. Nacareniobsite-(Ce) is now known to be of more widespread occurrence in some hyper-agpaitic rocks of the Ilímaussaq complex, and vitusite-(Ce) is known to be the precursor of the widespread occurrence of the yellow pseudomorphs termed erikite.


2014 ◽  
Vol 52 (2) ◽  
pp. 373-397 ◽  
Author(s):  
Maxime Baijot ◽  
Frédéric Hatert ◽  
Fabrice Dal Bo ◽  
Simon Philippo

1968 ◽  
Vol 5 (3) ◽  
pp. 455-482 ◽  
Author(s):  
E. W. Reinhardt

Phase relations among sillimanite, cordierite, garnet, biotite, and hypersthene from regionally metamorphosed pelitic gneisses were determined from petrographic studies and the chemical compositions of 46 ferromagnesian minerals and 18 bulk rocks. The compatible mineral associations including quartz, feldspar, and opaque oxides are cordierite-sillimanite, cordierite-garnet-sillimanite, cordierite-garnet-biotite, cordierite-garnet-hypersthene, cordierite-biotite-hypersthene, cordierite-biotite, garnet-biotite, garnet-biotite-hypersthene, and biotite-hypersthene. The assemblages were graphically analyzed using A–F–M diagrams derived from compatibility tetrahedra by successive projections through the common phases quartz, alkali feldspar, plagioclase, magnetite, and ilmenite; this results in the subtraction of excess components such that A = Al2O3 − K2O − Na2O − CaO, F = FeO − Fe2O3 − TiO2, and M = MgO. Variations in the positions of the three-phase triangles defined by cordierite, garnet, and biotite in the A–F–M system are due to systematic variations of F: M ratios for these minerals and reveal that the external conditions of metamorphism were variable over the rock sequence studied. Partitioning of elements among coexisting minerals and field evidence indicate that equilibrium was reached at constant temperature in the gneisses around Gananoque Lake; possible variations in load pressure were inadequate to cause the observed variations in F/M. A correlation between the Fe+2/(Fe+2 + Mg) of coexisting ferromagnesian silicates and the oxidation ratios (2Fe2O3/(2Fe2O3 + FeO)) of respective rocks suggests that the mineralogical variations in F/M are a function of oxygen partial pressure. Increased oxygen pressures would give rise to magnetite at the expense of the ferromagnesian silicates, which would consequently become enriched in the magnesium end-members. It is further proposed that the equilibrium partial pressures of oxygen and water were interdependent in any small volume of pelitic gneiss during metamorphism, and that [Formula: see text] was the independent variable.


Clay Minerals ◽  
2011 ◽  
Vol 46 (2) ◽  
pp. 279-294 ◽  
Author(s):  
G. Kirov ◽  
E. Šamajova ◽  
R. Nedialkov ◽  
TS. Stanimirova

AbstractThe genesis of the products of the alteration of acid pyroclastic material is discussed and interpreted on the basis of the distribution, sedimentation conditions, post-sedimentation activity, mineral and chemical compositions of pyroclastic deposits in Bulgaria and Slovakia.It is found that the disordered nonequilibrium nature of the volcanic glass induces a diagenetic devitrification of the tuffs and formation of clinoptilolitic, adularia-cristobalite and bentonite rocks. With increasing temperature, the volcanic glass tends forward a stable state through a series of zeolite mineral associations: clinoptilolite-mordenite-analcime-feldspar. The change in mineral composition of this series of rocks occurs without a change in the chemical composition of the rocks, which could be explained by the closed nature of zeolite systems. The formation of bentonites is associated with the removal of alkaline ions under diagenetic conditions, while the formation of halloysite rocks is caused by hydrothermal activity.


Author(s):  
D.I. Potter ◽  
M. Ahmed ◽  
K. Ruffing

Ion implantation, used extensively for the past decade in fabricating semiconductor devices, now provides a unique means for altering the near-surface chemical compositions and microstructures of metals. These alterations often significantly improve physical properties that depend on the surface of the material; for example, catalysis, corrosion, oxidation, hardness, friction and wear. Frequently the mechanisms causing these beneficial alterations and property changes remain obscure and much of the current research in the area of ion implantation metallurgy is aimed at identifying such mechanisms. Investigators thus confront two immediate questions: To what extent is the chemical composition changed by implantation? What is the resulting microstructure? These two questions can be investigated very fruitfully with analytical electron microscopy (AEM), as described below.


Author(s):  
Gejing Li ◽  
D. R. Peacor ◽  
D. S. Coombs ◽  
Y. Kawachi

Recent advances in transmission electron microscopy (TEM) and analytical electron microscopy (AEM) have led to many new insights into the structural and chemical characteristics of very finegrained, optically homogeneous mineral aggregates in sedimentary and very low-grade metamorphic rocks. Chemical compositions obtained by electron microprobe analysis (EMPA) on such materials have been shown by TEM/AEM to result from beam overlap on contaminant phases on a scale below resolution of EMPA, which in turn can lead to errors in interpretation and determination of formation conditions. Here we present an in-depth analysis of the relation between AEM and EMPA data, which leads also to the definition of new mineral phases, and demonstrate the resolution power of AEM relative to EMPA in investigations of very fine-grained mineral aggregates in sedimentary and very low-grade metamorphic rocks.Celadonite, having end-member composition KMgFe3+Si4O10(OH)2, and with minor substitution of Fe2+ for Mg and Al for Fe3+ on octahedral sites, is a fine-grained mica widespread in volcanic rocks and volcaniclastic sediments which have undergone low-temperature alteration in the oceanic crust and in burial metamorphic sequences.


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