TY - JOUR A1 - Thomas, Rainer A1 - Webster, J. D. A1 - Rhede, Dieter A1 - Seifert, W. A1 - Rickers, Karen A1 - Förster, Hans-Jürgen A1 - Heinrich, Wilhelm A1 - Davidson, P. T1 - The transition from peraluminous to peralkaline granitic melts: Evidence from melt inclusions and accessory minerals JF - Lithos : an international journal of mineralogy, petrology, and geochemistry N2 - Fractional crystallization of peraluminous F- and H(2)O-rich granite magmas progressively enriches the remaining melt with volatiles. We show that, at saturation, the melt may separate into two immiscible conjugate melt fractions, one of the fractions shows increasing peraluminosity and the other increasing peralkalinity. These melt fractions also fractionate the incompatible elements to significantly different degrees. Coexisting melt fractions have differing chemical and physical properties and, due to their high density and viscosity contrasts, they will tend to separate readily from each other. Once separated, each melt fraction evolves independently in response to changing T/P/X conditions and further immiscibility events may occur, each generating its own conjugate pair of melt fractions. The strongly peralkaline melt fractions in particular are very reactive and commonly react until equilibrium is attained. Consequently, the peralkaline melt fraction is commonly preserved only in the isolated melt and mineral inclusions. We demonstrate that the differences between melt fractions that can be seen most clearly in differing melt inclusion compositions are also visible in the composition of the resulting ore-forming and accessory minerals, and are visible on scales from a few micrometers to hundreds of meters. KW - granite melts KW - magma evolution KW - melt inclusions KW - melt-melt immiscibility KW - peraluminosity KW - peralkalinity KW - accessory minerals Y1 - 2006 U6 - https://doi.org/10.1016/j.lithos.2006.03.013 SN - 0024-4937 VL - 91 IS - 1-4 SP - 137 EP - 149 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Seifert, Wolfgang A1 - Rhede, Dieter A1 - Förster, Hans-Jürgen A1 - Thomas, Rainer T1 - Accessory minerals as fingerprints for the thermal history and geochronology of the Caledonian Rumburk granite N2 - 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. Y1 - 2009 UR - http://www.ingentaconnect.com/content/schweiz/njma U6 - https://doi.org/10.1127/0077-7757/2009/0147 SN - 0077-7757 ER - TY - JOUR A1 - Keutsch, Frank N. A1 - Förster, Hans-Jürgen A1 - Stanley, Chris J. A1 - Rhede, Dieter T1 - The discreditation of hastite, the orthorhombic dimorph of CoSe2, and observations on trogtalite, cubic CoSe2, from the type locality N2 - "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. Y1 - 2009 UR - http://www.canmin.org/ U6 - https://doi.org/10.3749/canmin.47.4.969 SN - 0008-4476 ER - TY - JOUR A1 - Grüneberger, Anja Maria A1 - Schmidt, Christian A1 - Jahn, Sandro A1 - Rhede, Dieter A1 - Loges, Anselm A1 - Wilke, Max T1 - Interpretation of Raman spectra of the zircon-hafnon solid solution JF - European journal of mineralogy N2 - Zircon (ZrSiO4), hafnon (HfSiO4) and five intermediate compositions were synthesized from a Pb silicate melt. The resulting crystals were 20-300 mu m in size and displayed sector and growth zoning. Raman spectra were acquired at locations in the sample for which preceding electron microprobe (EMP) analyses revealed sufficient compositional homogeneity. The dataset documents shifts of Raman bands with changing composition. In this study, bands that have previously not been reported were found for the intermediate compositions and for pure hafnon, in particular at wavenumbers less than 200 cm(-1). For these external modes, the dataset provides new insight into the compositional dependence of their frequencies. Density-functional theory calculations support the observations and are used for a detailed interpretation of the spectra. The pitfalls of the EMP analysis along the zircon-hafnon join are highlighted. KW - zircon KW - hafnon KW - solid solution KW - Raman spectroscopy KW - synthesis KW - density-functional theory KW - hafnium analysis Y1 - 2016 U6 - https://doi.org/10.1127/ejm/2016/0028-2551 SN - 0935-1221 SN - 1617-4011 VL - 28 SP - 721 EP - 733 PB - Schweizerbart CY - Stuttgart ER - TY - JOUR A1 - Förster, Hans-Jürgen A1 - Tischendorf, Gerhard A1 - Rhede, Dieter A1 - Naumann, R. A1 - Gottesmann, Bärbel A1 - Lange, W T1 - Cs-rich lithium micas and Mn-rich lithian siderophyllite in miarolitic NYF pegmatites of the Konigshain granite, Lausitz, Germany N2 - 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) Y1 - 2005 ER - TY - JOUR A1 - Förster, Hans-Jürgen A1 - Tischendorf, Gerhard A1 - Rhede, Dieter T1 - Mineralogy of the Niederschlema-Alberoda U-Se-polymetallic deposit, Erzgebirge, Germany. v. watkinsonite, nevskite, bohdanowiczite and other bismuth minerals N2 - 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 Y1 - 2005 ER - TY - JOUR A1 - Förster, Hans-Jürgen A1 - Romer, Rolf L. A1 - Gottesmann, Bärbel A1 - Tischendorf, Gerhard A1 - Rhede, Dieter T1 - Are the granites of the Aue-Schwarzenberg Zone (Erzgebirge, Germany) a major source for metalliferous ore deposits? : a geochemical, Sr-Nd-Pb isotopic, and geochronological study N2 - 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. Y1 - 2009 UR - http://www.schweizerbart.de/j/n-jb-min/ U6 - https://doi.org/10.1127/0077-7757/2009/0138 SN - 0077-7757 ER - TY - JOUR A1 - Förster, Hans-Jürgen A1 - Rhede, Dieter A1 - Tischendorf, Gerhard T1 - Mineralogy of the Niederschlema-Alberoda U-Se-polymetallic deposit, Erzgebirge, Germany : I. Jolliffeite, NiAsSe, the rare Se-dominant analogue of gersdorffite N2 - 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 Y1 - 2004 ER - TY - JOUR A1 - Förster, Hans-Jürgen A1 - Rhede, Dieter T1 - The Be-Ta-rich granite of Seiffen (eastern Erzgebirge, Germany) BT - accessory-mineral chemistry, composition, and age of a late-Variscan Li-F granite of A-type affinity JF - Neues Jahrbuch für Mineralogie : Abhandlungen N2 - 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. KW - Li-F granite KW - Th-U-Pb monazite age KW - beryllium KW - tantalum KW - ytterbian xenotime-(Y) KW - ongonite KW - post-collisional setting Y1 - 2006 U6 - https://doi.org/10.1127/0077-7757/2006/0055 SN - 0077-7757 VL - 182 IS - 3 SP - 307 EP - 321 PB - Schweizerbart CY - Stuttgart ER - TY - JOUR A1 - Förster, Hans-Jürgen A1 - Rhede, Dieter T1 - Mineralogy of the Niederschlema-Alberoda U-Se-polymetallic deposit, Erzgebirge, Germany : III. First indication of complete miscibility between tennantite and giraudite Y1 - 2004 ER -