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The strongly peraluminous and P-rich, protolithionite and zinnwaldite leucogranites from Podlesi, western Krusne Hory Mts., Czech Republic, contain accessory zircon with extraordinary enrichment of several elements, which constitute trace elements in common zircon. Elements showing a not yet reported anomalous enrichment include P (up to 20.2 wt.% P2O5; equivalent to 0.60 apfu, formula calculated on the basis of 4 oxygen atoms), Bi (up to 9.0 wt.% Bi2O3; 0.086 apfu), Nb (up to 6.7 wt.% Nb2O5, 0.12 apfu), Sc (up to 3.45 wt.% Sc2O3; 0.10 apfu), U (up to 14.8 wt.% UO2; 0.12 apfu) and F (up to 3.81 wt.% F; 0.42 apfu). Strong enrichment of P preferentially involved the berlinite-type substitution (2 Si4+ double left right arrow P5+ + Al3+) implying that significant Al may enter the Si position in zircon. Incorporation of other exotic elements is primarily governed by the xenotime (Si4++Zr4+ double left right arrow P5++Y3+), pretulite (Sc3++P5+ double left right arrow Zr4++Si4+), brabantite-type (Ca2++(U, Th)(4+)+2P(5+) double left right arrow 2Zr(4+)+2Si(4+)), and ximengite-type (Bi3++P5+double left right arrow Zr4++Si4+) substitution reactions. One part of the anomalous zircons formed late-magmatically, from a strongly peraluminous, P-F-U-rich hydrous residual melt that gave rise to the zinnwaldite granite. Interaction with aggressive residual fluids and metamictization have further aided in element enrichment or depletion, particularly in altered parts of zircon contained in the protolithionite granite. Most of the zircon from F-rich greisens have a composition close to endmember ZrSiO4 and are chemically distinct from zircon in its granite parent. This discrepancy implies that at Podlesi, granitic zircon became unstable and completely dissolved during greisenization. Part of the mobilized elements was reprecipitated in newly grown, hydrothermal zircon.
Thermal conductivity (lambda) is an essential physical property of minerals and rocks and fundamental in constraining the thermal field of the lithosphere. In case that adequate samples to measure lambda are not available, it could be indirectly inferred from calculation. One of the most widely applied indirect methods for rocks involve modal mineralogy and porosity as parameters that are incorporated into mathematical mean or mixing models. Robust inferences from these approaches for crystalline rocks were impeded by a small number of studied samples or restriction to certain rock types. We employ this method and examine its applicability to low-porosity plutonic rocks by calculating bulk thermal conductivity lambda(b) for 45 samples covering the entire range from gabbro/diorite to granite. We show that the use of the harmonic-mean model for both rock matrix and porosity provided a good match between lambda(b.meas) and lambda(b.calc) of <10% deviation (2 sigma), with relative and absolute errors amounting to 1.49.7% and 4.44.9%, respectively. The results of our study constitute a big step forward to a robust conclusion on the overall applicability of the harmonic-mean model for inferring lambda(b) of isotropic, low-porosity, mafic to silicic plutonic and metamorphic rocks with an acceptable magnitude of error. Drill cuttings and enclaves form particularly interesting objects for application of this method, as they are poorly suited for direct measurement. Well-derived lambda values for those rocks would permit to calculate heat flow and to model more profoundly the thermal state of the deeper lithosphere.
A comprehensive survey of the accessory-mineral assemblages in Variscan granites of the German Erzgebirge and Pan-African granites from Jordan revealed the occurrence of intermediate solid solutions of the tetragonal thorite- xenotime-zircon-coffinite mineral group with partially novel compositions. These solid solutions preferentially formed in evolved and metasomatically altered, P-poor leucogranites of either I- or A-type affinity. Thorite from the Erzgebirge contained up to 18-8 Wt-% Y2O3, 16.1 wt.% ZrO2, and 23.3 Wt-% UO2. Xenotime and zircon have incorporated Th in abundances up to 36.3 wt.% and 41.8 wt.% ThO2, respectively. Extended compositional gradation with only minor gaps is confined to hydrated members of this mineral group, and is observed to exist between thorite and xenotime, thorite and coffinite, and Y-HREE-bearing thorite and zircon. Complex, hydrous solid solutions containing elevated abundances of three or more of the endmembers are subordinate. Previously reported intermediate solid solutions between anhydrous zircon and xenotime, and anhydrous zircon and thorite, are not observed and are in conflict with experimental work demonstrating very limited miscibility between anhydrous species of endmember composition. The majority of hydrous intermediate solid solutions in the Th-Y-Zr-U system are likely thermodynamically unstable. Instead, they are probably metastable responses to unusual physico-chemical conditions involving various parameters and conditions, the relative importance of which is incompletely known. Leaching and dissolution of preexisting accessory phases during interaction with F-bearing hydrous fluids enriched in Th, Y(HREE), Zr, and/or U, and common deposition of the various elements at disequilibrium (supersaturation) seems to play a key role, but other processes may be of similar importance. Experimental work involving hydrous conditions and complex systems composed of more than two endmembers are needed to shed light into the stability relations of the chemically uncommon compositions treated in this study.
In a sample from the Niederschlema-Alberoda U-Se-polymetallic deposit, western Erzgebirge, Germany, the entire PbSe-PbS solid-solution series was observed associated with uraninite, coffinite, hematite, acanthite, sphalerite, chalcopyrite, pyrite, and lollingite. Early deposited, Se-rich members of the Pb(Se, S) series occur as fracture fillings inside spherical uraninite or on its surface or form anhedral to subhedral grains precipitated in the immediate neighbourhood of the U minerals. Later crystallized, S-rich members of the series are affiliated with the sulfide minerals. The solid-solution series covers the range PbS1.00-Pb(S0.04Se0.96)(&USigma; 1.00) virtually free of gaps, consistent with a temperature of formation of &GE; 100° C. The PbSe-PbS solid solutions were likely deposited from hydrothermal fluids that became successively depleted in Se and enriched in S. The fugacities of selenium and sulfur covered the range -17 < logfSe(2) < -26 and -17 < logfS(2) < -22, respectively, implying fSe(2)/fS(2) &LE; 1. The spherical texture of the uraninite, as well as its U-Th-total Pb age (192 ± 21 Ma), imply deposition of the Pb(Se, S) series during the Jurassic, contemporaneous with the formation of the bulk of the other selenium minerals. The electron-microprobe data from this study confirm earlier inferences on complete miscibility between clausthalite and galena deduced from X-ray patterns of PbSe-PbS solid solutions from different uranium-vanadium deposits of the Colorado Plateau (COLEMAN 1959). In Niederschlema-Alberoda, the entire clausthalite-galena series occurs in a single section
Hessite, Ag2Te, and native tellurium (?) constitute two, previously unknown tellurium species within the complex mineral assemblage at Niederschlema-Alberoda, Erzgebirge, Germany. Hessite is always intimately associated with clausthalite and has a composition close to ideal stoichiometry. The mean empirical formula is (Ag1.98Sb0.01)(1.99)(Te0.96Se0.05)(1.01). Paragenetic relations and thermodynamic data suggest that hessite crystallized in equilibrium with clausthalite, berzelianite, and tiemannite under conditions of almost identical, high fugacitities of Se-2 and Te-2, which very locally were approached in the main selenide stage of Jurassic age. Native tellurium (?) formed as replacement product of hessite. Niederschlema-Alberoda provides the first record of hessite from an uranium deposit worldwide. Hessite and native Te are the first tellurium minerals reported from the Erzgebirge metallogenic province
In this paper, a unique set of samples from the uppermost crust down to the lithospheric mantle of Jordan is analyzed for composition and petrophysical properties (density. thermal conductivity, radiogenic heat production) These data, covering a vertical section of almost 65 km. are used in conjunction with surface heat flow to generate a detailed and comprehensive lithospheric thermal model that reflects the conditions of the Arabian Shield (AS) prior to the post- Oligocene onset of lithosphere thinning and Voluminous basaltic volcanism. The pre-Miocene model geotherms, based on conductive surface heat flows of 55 and 60 mW m(-2). (a) meet the range of lithosphere-asthenosphere boundary depths of 110-160 km known from seismology, (b) conform to results of thermomechanical models on the on.-in of the Dead Sea basin that started in Miocene time. and (c) are consistent with typical xenolith-derived geotherms for terranes of similar age and lithospheric thickness. Moho temperatures (at depths between 35 and 40 km) of the AS in pre-Miocene times were most likely in the order of 530-650 degrees C, with mantle heat flows averaging between 24 and 29 mW m(-2) Results contradict former views of the late Proterozoic/early Cambrian-stabilized AS being an anomalously cold terrane A "cold" thermal structure inferred from previously measured low surface heat flows (generally <= 45 mW m(-2)) is inconsistent with the thickness, composition, and petrophysical properties of the stable lithosphere of the shield.
The mildly peraluminous granite of Seiffen, in the eastern Erzgebirge of Germany, is exposed by drillcores and associated with an abandoned Sri mine. The granite is of Stefanian age, with overlapping Th-U-total Pb monazite (302 +/- 4 Ma) and K-Ar siderophyllite ages (301 +/- 5 Ma). It is among the youngest granites in the Erzgebirge, emplaced in an extensional setting. The medium-grained, equigranular granite classifies as high-F, low-P Li-mica granite of A-type affinity. It is spatially associated with a high-Si rhyolitic microgranite, documenting the shallow intrusion level of this igneous association. Zircon, monazite-(Ce), and xenotime-(Y) constitute important radioactive accessory minerals in the granite, hosting the major proportions (> 80-90%) of the bulk-rock budgets of the REE, Y, and Th. A significant percentage of U (40-50%) may reside within unidentified phases or precipitated along grain boundaries. The most uncommon accessory phase is late-magmatic ytterbian xenotime-(Y) containing up to 11.2 wt% Yb2O3, in addition to 7.3 wt% Er2O3 and 7.9 wt% Dy2O3. The Seiffen granite (epsilon(Nd(300)) = -4.6) is geochemically evolved and rich in Sri (23-63 ppm) and W (11-14 ppm). It contains elevated to high concentrations of incompatible lithophile elements such as F, Li, Ga, Rb, Y, Nb, Cs, REE, Th, and U, thus having much in common chemically with subvolcanic ongonites. The most prominent compositional feature is the strong enrichment (in ppm) in Be (51-55) and Ta (23-28). The granite exhibits flat chondrite-normalized REE patterns (La-N/Lu-N = 1.35-1.48) and a moderate negative Eu anomaly (Eu/Eu* = 0.12-0.13). Indications for alteration-induced, postmagmatic disturbances of initial elemental abundances are weak and mainly relate to the ore-forming elements Sri and U.
The Niederschlema-Alberoda uranium deposit, in the Erzgebirge region of Germany, contains an uncommon assemblage of metallic minerals, in particular selenides, sulfides, arsenides, tellurides, and native elements, in addition to uraninite and coffinite. The complex mineralogy resulted from the superposition of several mineralizing events over the time interval from the Permian to the Cretaceous; these events introduced and redeposited a great variety of metallic elements within the hydrothermal uranium deposit (Pb, Ag, Cu, Hg, Tl, Bi, Co, Ni, As, Sb, Se, S, Te). One of the exotic minerals is jolliffeite, an arsenoselenide with end-member composition NiAsSe, so far only known from Lake Athabasca, Saskatchewan, Canada. A single, small, anhedral grain of jolliffeite from Niederschlema-Alberoda is included and partly replaced by sulfurian eskebornite. Associated minerals comprise hematite, Ni-Co-Se-bearing lollingite, clausthalite, tiemannite, mercurian hakite-giraudite solid solutions, sulfurian berzelianite, sulfurian umangite, hessite, Ni-Co-As-bearing pyrite, and Se-rich chalcopyrite. The sulfurian jolliffeite has the empirical formula (Ni0.85Cu0.09Co0.05Fe0.02Ag0.01)Sigma(1.02)As(0.98)(Se0.77S0.23)(Sigma1. 00) and differs from type jolliffeite mainly by substantial substitution of Cu (2.6-3.3 wt.%) for Ni and S (3.2-4.1 wt.%) for Se. Substantial S-for-Se substitution in jolliffeite implies extensive and probably complete miscibility between NiAsSe and its S-dominant analogue, gersdorffite-Pa3 (NiAsS). We suggest that a localized accumulation of Ni and As in the Se-(S)-bearing hydrothermal fluid gave rise to the crystallization of jolliffeite at some rare locations at a late stage of formation of the Jurassic selenide assemblage
The Aue-Schwarzenberg Granite Zone (ASGZ), in the western Erzgebirge of Germany, is composed of small, late- Variscan F-poor biotite and two-mica granites. The biotite granites (Aue granite suite, Beierfeld, Bernsbach) are weakly to mildly peraluminous (A/CNK = 1.07-1.14; 70-76 wt% SiO2), display similar Sr-87/Sr-86 initial ratios (0.7065-0.7077; t = 325 Ma), and exhibit a narrow range in epsilon Nd-325 (-2.6 to -3.5). They are closely affiliated compositionally with the biotite granites in the distant, more voluminous Nejdek massif (Czech Republic). The two-mica granites (Schwarzenberg granite suite, Lauter) are Si-rich (74-77 wt% SiO2) and mildly to strongly peraluminous (A/CNK = 1.17- 1.26). The granites from Schwarzenberg Lire distinctly higher in their Sr(i)ratios (0.709-0.713; t = 325 Ma) and possess lower values of epsilon Nd-325 (-4.9 to -5.2) relative to the biotite granites. The Lauter granites have a Nd-isotopic composition between -3.6 and -4.0 (t = 325 Ma). Mean Th-U-total Pb uraninite ages (Ma +/- 2 sigma) obtained for the granites from the Aue Suite (324.3 +/- 3. 1), Beierfeld (323.7 +/- 3.1), Bernsbach (320.7 +/- 2.9), Schwarzenberg (323.3 +/- 2.4), and the Kirchberg granite al Burkersdorf (322.7 +/- 3.5) indicate that magmatism in the ASGZ commenced in the Namurian and took place early within the major episode of granite formation in the Erzgebirge-Vogtland zone (327-318 Ma). Geochemical and mineralogical patterns of variably altered samples imply that the ASGZ granites are unlikely to have significantly contributed to the formation of spatially associated metalliferous ore deposits (Sn, W, Mo, Ph, Zn, Bi, Co, Ni), except for uranium. In particular the Aue granite suite should have served as major Source for U accumulated in the economically important post-granitic deposits of Schneeberg and Schlema-Alberoda.
The uranium deposit at Niederschlema-Alberoda, Germany, contains a rich variety of Bi minerals deposited between the Permian and the Cretaceous; these have been studied for paragenetic relations, composition, and conditions of formation. Particular attention is given to the rare Bi selenides watkinsonite, nevskite, and cuproan bohdanowiczite. Whereas watkinsonite and nevskite only occur intergrown with clausthalite, bohdanowiczite is more widespread and also is associated with Cu selenides. Watkinsonite from this second confirmed locality worldwide has an average composition (Cu1.47Ag0.49)(Sigma 1.96)(Pb1.01Hg0.01 Fe-0.01)(Sigma 1.03)Bi-3.98(Se7.98S0.05)(Sigma 8.03), ideally (Cu,Ag)(2)PbBi4Se8. These findings suggest that the empirical formula of watkinsonite originally proposed for the type specimen from the Otish Mountains uranium deposit in Quebec [CU2+xPb1+xBi4-xSe,S,Te)(8), x approximate to 0.3] requires revision. The composition of nevskite is (Pb0.06Bi0.95)(Sigma 1.01)Se-0.99, on average. Bohdanowiczite from the Cu- selenide assemblage shows extensive substitution of Cu+ for Ag+, expressed by the crystallochemical formula (Ag1.80- 0.94CU0.16-1.05Pb0.00-0.05)(Sigma 1.97-2.07)BiSigma 1.97-2.03SeSigma 3.96-4.04. This observation seems to argue for the natural existence of CU2Bi2Se4, the Se-dominant analogue of emplectite. The Bi selenides were deposited at temperatures of about 100 degrees C, in the Jurassic. The lack of thermodynamic data for all the Bi selenides limits reliable inferences on the fugacities of selenium and sulfur that prevailed during their formation. Other Bi minerals from this locality comprise members of the bismuthinite-aikinite solid-solution series of Permian age and, more importantly, native Bi and Bi sulfides (matildite, bismuthinite, wittichinite), deposited in the Cretaceous
Annite and Fe-rich siderophyllite constitute the rock-forming micas in the late-Variscan composite granite pluton of Konigshain, Lausitz, Germany. This multiphase pluton is composed of three fractionated, but not chemically specialized monzogranite types, which contain lithophile elements such as Li, Rb, Cs, Sn, and F in average quantities. Abundant miarolitic pegmatites of the NYF family with a broad diversity of rare minerals occur in the apical part of the pluton. These pegmatitic cavities locally contain di- and trioctabedral micas as well as cation-deficient micas. Trioctahedral micas comprise F-rich manganoan lithian siderophyllite to manganoan zinnwaldite, zinnwaldite, and minor lepidolite. The formula [calculated on the basis of 22 anion valencies and 2 (F + OH + Cl)] of the most Mn-rich siderophyllite is (K0.85Rb0.08Na0.04)(0.97)(Al0.99Li0.91Fe0.51Mn0.42Ti0.01Zn0.01)(2.85) (Si3.21Al0.79)(4)O- 10(F1.80OH0.19Cl0.01)(2). This mica constitutes one of the most Mn-rich siderophyllite compositions reported to date. The lithium micas poorer in Mn are distinguished by elevated concentrations of Rb (up to 2.5 wt % Rb2O), CS (UP to 1.2 wt % Cs2O), and F (up to 9.6 wt %). This fluorine content is probably consistent with the maximum possible F occupation of 2 of the (F,OH,Cl)-site. The structural formula of the most Li-rich lepidolite is (K0.83Rb0.07Cs0.03)(0.93) (Li1.62Al1.00Fe0.38)(3.00)(Si3.62Al0.38)(4) O-10(F1.91OH0.09)(2). During hydrothermal alteration, lepidolite and zinnwaldite became partially depleted in K, Li, Rb, Cs, and F and gradually transformed into cation-deficient micas (lithian phengite to illite of phengitic affinity)
In the earliest emplaced granite subintrusion of the multiphase peraluminous Satzung pluton, Erzgebirge, Germany, a mineral aggregate was observed consisting of sekaninaite (X-Fe = 0.74-0.94), Zn-rich hercynite (X-Zn = 0.03- 0.11), tri- and dioctahedral layer silicates of different composition and color, and minor quartz. Geological, textural, and compositional criteria argue that the sekaninaite, hercynite, quartz, and the brown biotite are not primary or secondary granite minerals, but are of metamorphic origin representing a xenolith uptaken from the granite melt near its level of emplacement. The metamorphic origin is supported by the occurrence of this mineral assemblage in metamorphic rocks exposed locally in the Erzgebirge basement. Reaction of the polymineralic metamorphic aggregate with the surrounding melt and subsequent interaction with alkali-, F- and LILE-rich residual fluids account for the widespread decomposition of the sekaninaite and formation of several layer silicates including green biotite, muscovite, berthierine/Fe chlorite, and sericite. The observed enrichment of the relic sekaninaite and its replacement products in elements such as Na, Li, Be, Rb, Cs, and F is result of interaction of the metamorphic fragment with the surrounding melt/fluid, in accordance with the evolved nature of the Satzung magmatic-hydrothermal system
A localized dehydration zone, Sondrum stone quarry, Halmstad, SW Sweden, consists of a central, 1 m wide granitic pegmatoid dyke, on either side of which extends a 2.5-3 m wide dehydration zone (650-700 degrees C; 800 MPa; orthopyroxene-clinopyroxene-biotite-amphibole-garnet) overprinting a local migmatized granitic gneiss (amphibole-biotite- garnet). Whole-rock chemistry indicates that dehydration of the granitic gneiss was predominantly isochemical. Exceptions include [Y + heavy rare earth elements (HREE)], Ba, Sr, and F, which are markedly depleted throughout the dehydration zone. Systematic trends in the silicate and fluorapatite mineral chemistry across the dehydration zone include depletion in Fe, (Y + HREE), Na, K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusion chemistry is similar in all three zones and indicates the presence of a fluid containing CO2, NaCl, and H2O components. Water activities in the dehydration zone average 0.36, or XH2O = 0.25. All lines of evidence suggest that the formation of the dehydration zone was due to advective transport of a CO2-rich fluid with a minor NaCl brine component originating from a tectonic fracture. Fluid infiltration resulted in the localized partial breakdown of biotite and amphiboles to pyroxenes releasing Ti and Ca, which were partitioned into the remaining biotite and amphibole, as well as uniform depletion in (Y + HREE), Ba, Sr, Cl, and F. At some later stage, H2O-rich fluids (H2O activity > 0.8) gave rise to localized partial melting and the probable injection of a granitic melt into the tectonic fracture, which resulted in the biotite and amphibole recording a diffusion profile for F across the dehydration zone into the granitic gneiss as well as a diffusion profile in Fe, Mn, and Mg for all Fe-Mg silicate minerals within 100 cm of the pegmatoid dyke
Reaction rims of titanite on ilmenite are described in samples from four terranes of amphibolite-facies metapelites and amphibolites namely the Tamil Nadu area, southern India; the Val Strona, area of the Ivrea-Verbano Zone, northern Italy, the Bamble Sector, southern Norway, and the northwestern Austroalpine Otztal Complex. The titanite rims, and hence the stability of titanite (CaTiSiO4O) and Al-OH titanite, i.e. vuaganatite (hypothetical end-member CaAlSiO4OH), are discussed in the light of fH(2)O- and fO(2)-buffered equilibria involving clinopyroxene, amphibole, biotite, ilmenite, magnetite, and quartz in the systems CaO-FeO/Fe2O3-TiO2-SiO2-H2O-O-2 (CFTSH) and CaO-FeO/Fe2O3-Al2O3- SiO2-H2O-O-2 (CFASH) present in each of the examples. Textural evidence suggests that titanite reaction rims on ilmenite in rocks from Tamil Nadu, Val Strona, and the Bamble Sector originated most likely due to hydration reactions such as clinopyroxene + ilmenite +quartz+ H2O = amphibole +titanite and oxidation reactions such as amphibole + ilmenite + O-2 = titanite + magnetite + quartz + H2O during amphibolite-facies metamorphism, or, as in the case of the Otztal Complex, during a subsequent greenschist-facies overprint. Overstepping of these reactions requires fH(2)O and fO(2) to be high for titanite formation, which is also in accordance with equilibria involving Al-OH titanite. This study shows that, in addition to P, T, bulk-rock composition and composition of the coexisting fluid, fO(2) and fH(2)O also play an important role in the formation of Al-bearing titanite during amphibolite- and greenschist-facies metamorphism.
In a series of timed experiments, monazite inclusions are induced to form in the Durango fluorapatite using 1 and 2 N HCl and H2SO4 solutions at temperatures of 300, 600, and 900 degrees C and pressures of 500 and 1,000 MPa. The monazite inclusions form only in reacted areas, i.e. depleted in (Y+REE)+Si+Na+S+Cl. In the HCl experiments, the reaction front between the reacted and unreacted regions is sharp, whereas in the H2SO4 experiments it ranges from sharp to diffuse. In the 1 N HCl experiments, Ostwald ripening of the monazite inclusions took place both as a function of increased reaction time as well as increased temperature and pressure. Monazite growth was more sluggish in the H2SO4 experiments. Transmission electron microscopic (TEM) investigation of foils cut across the reaction boundary in a fluorapatite from the 1 N HCl experiment (600 degrees C and 500 MPa) indicate that the reacted region along the reaction front is characterized by numerous, sub-parallel, 10-20 nm diameter nano-channels. TEM investigation of foils cut from a reacted region in a fluorapatite from the 1 N H2SO4 experiment at 900 degrees C and 1,000 MPa indicates a pervasive nano- porosity, with the monazite inclusions being in direct contact with the surrounding fluorapatite. For either set of experiments, reacted areas in the fluorapatite are interpreted as replacement reactions, which proceed via a moving interface or reaction front associated with what is essentially a simultaneous dissolution-reprecipitation process. The formation of a micro- and nano-porosity in the metasomatised regions of the fluorapatite allows fluids to permeate the reacted areas. This permits rapid mass transfer in the form of fluid-aided diffusion of cations to and from the growing monazite inclusions. Nano-channels and nano-pores also serve as sites for nucleation and the subsequent growth of the monazite inclusions
"Hastite", the orthorhombic dimorph of CoSe2, formerly considered as a valid mineral species occurring in the Trogtal quarries, Harz Mountains, Germany, is discredited as being identical with ferroselite, orthorhombic FeSe2. The discreditation has been unanimously approved by the IMA Commission on New Minerals, Nomenclature and Classification (CNMNC) (IMA No. 07-E). We also provide observations on the composition, homogeneity, and origin of trogtalite (cubic CoSe2) from its type locality.
Accessory minerals of the Caledonian Rumburk granite are investigated to gain insight into its magmatic and post-magmatic evolution history. Recent geothermometers calibrated for trace elements in rutile (Zr), zircon (Ti), and quartz (Ti) were used to determine mineral-formation temperatures, which are compared with T data obtained from melt and fluid-inclusion Studies on quartz. Improved electron-microprobe analytical conditions allowed distinguishing several generations of rutile. Submicron-sized rutile needles included in quartz crystallized at around 739 +/- 13 degrees C and, thus, are evidently magmatic. Simultaneous crystallization of the high-T rutile and quartz is the favoured concept compared with an exsolution model for the needles. Th-U-total Pb dating of xenotime-(Y) by electron microprobe yielded a bimodal age distribution of 494 +/- 8 Ma (2 sigma; n = 44) and 311 +/- 8 Ma (2 sigma; n = 48), which is missing in monazite-(Ce). The older age correlates with the early Ordovician granite emplacement age Suggested by earlier isotopic Studies. The younger Carboniferous age also may be geologically reasonable, because the granite experienced a minor tectonothermal overprint during the Variscan orogenesis. However, whether this event has caused the resetting of the isotopic system in the xenotime is uncertain. This also holds for the age of the partial breakdown of monazite and xenotime into reaction coronas composed of fluorapatite, allanite-(Ce), epidote +/- clinozoisite. This alteration assemblage was likely produced already during autometasomatic reworking of the solidifying magma in Ordovician time, but it cannot be excluded that it relates to a Carboniferous fluid imprint connected with late-Variscan processes.
Quartz crystals from topaz-zinnwaldite-albite granites from Zinnwald (Erzgebirge, Germany) contain, in addition to primary and secondary fluid inclusions (FIs), abundant crystalline silicate-melt inclusions (MIs) with diameters up to 200 mum. These MIs represent various stages of evolution of a highly evolved melt system that finally gave rise to granite-related Sn-W mineralization. The combination of special experimental techniques with confocal laser Raman- microprobe spectroscopy and EMPA permits precise measurement of elevated contents of H2O, F, and B in re-homogenized MIs. The contents of H2O and F were observed to increase from 3 to 30 and 1.9 to 6.4 wt%, respectively, during magma differentiation. However, there is a second MI group, very rich in H2O, with values up to 55 wt% H2O and an F concentration of approximately 3 wt%. Ongoing enrichment of volatiles H2O, F, B, and Cl and of Cs and Rb can be explained in terms of magma differentiation triggered by fractional crystallization and thus, is suggested to reflect elemental abundances in natural magmas, and not boundary-layer melts. Partitioning between melt and cogenetic fluids has further modified the magmatic concentrations of some elements, particularly Sn. The coexistence of two types of MIs with primary FIs indicates fluid saturation early in the history of magma crystallization, connected with a continuous sequestration of Sn, F, and B. The results of this study provide additional evidence for the extraordinary importance of the interplay of H2O, F, and B in the enrichment of Sn during magma differentiation by decreasing the viscosity of and increasing the diffusivity in the melts as well as by the formation of various stable fluoride complexes in the melt and coexisting fluid