@article{FoersterRhedeTischendorf2004,
  author    = {F{\"o}rster, Hans-J{\"u}rgen and Rhede, Dieter and Tischendorf, Gerhard},
  title     = {Mineralogy of the Niederschlema-Alberoda U-Se-polymetallic deposit, Erzgebirge, Germany : I. Jolliffeite, NiAsSe, the rare Se-dominant analogue of gersdorffite},
  year      = {2004},
  abstract  = {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},
  language  = {en}
}
@article{Foerster2004,
  author    = {F{\"o}rster, Hans-J{\"u}rgen},
  title     = {Mineralogy of the Niederschlema-Alberoda U-Se-polymetallic deposit, Erzgebirge, Germany : II: Hessite, Ag2Te, and native Te (?), the first tellurium minerals},
  year      = {2004},
  abstract  = {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},
  language  = {en}
}
@article{TischendorfRiederFoersteretal.2004,
  author    = {Tischendorf, Gerhard and Rieder, M. and F{\"o}rster, Hans-J{\"u}rgen and Gottesmann, B{\"a}rbel and Guidotti, C. V.},
  title     = {A new graphical presentation and subdivision of potassium micas},
  issn      = {0026-461X},
  year      = {2004},
  abstract  = {A system based on variation of the octahedrally coordinated cations is proposed for graphical presentation and subdivision of tri- and dioctahedral K micas, which makes use of elemental differences (in a.p.f.u.): (Mg - Li) [= mgli] and (Fe-tot + Mn + Ti - Al-VI) [= feal]. All common true tri- and dioctahedral K micas are shown in a single polygon outlined by seven main compositional points forming its vertices. Sequentially clockwise, starting from Mg-3 (phlogopite), these points are: Mg2.5Al0.5, Al(2.167)square(0.833), Al1.75Li1.25, Li2Al (polylithionite), Fe22+Li, and Fe-3(2+) (annite). Trilithionite (Li1.5Al1.5), Li1.5Fe2+Al0.5, Fe22+Mg, and Mg2Fe2+ are also located on the perimeter of the polygon. IMA-siderophyllite (Fe22+Al) and muscovite (Al(2)square) plot inside. The classification conforms with the IMA-approved mica nomenclature and differentiates among the following mica species according to their position in a diagram consisting of nigh and feal axes plotted orthogonally; trioctahedral: phlogopite, biotite, siderophyllite, annite, zinnwaldite, lepidolite and tainiolite: dioctahedral: muscovite, phengite and celadonite. Potassium micas with [Si] <2.5 a.p.f.u. including IMA-siderophyllite, KFe22+AlAl2Si2O10(OH)(2), and IMA-eastonite, KMg2AlAl2Si2O10(OH)(2) seem not to form in nature. The proposed subdivision has several advantages. All common true, trioctahedral and dioctahedral K micas, whether Li-bearing or Li-free, are shown within one diagram, which is easy to use and gives every mica composition an unambiguously defined name. Mica analyses with Fe2+, Fe3+, Fe2+ + Fe3+, or Fe-tot can be considered, which is particularly Valuable for microprobe analyses. It facilitates easy reconstruction of evolutionary pathways of mica compositions during crystallization, a feature having key importance in petrologically oriented research. Equally important, the subdivision has great potential for understanding many of the crystal-chemistry features of the K micas. In turn this may allow one to recognize and discriminate the extent to which crystal chemistry or bulk composition controls the occurrence of some seemingly possible or hypothetical K mica},
  language  = {en}
}
@article{WebsterThomasFoersteretal.2004,
  author    = {Webster, J. D. and Thomas, R. and F{\"o}rster, Hans-J{\"u}rgen and Seltmann, R. and Tappen, C.},
  title     = {Geochemical evolution of halogen-enriched granite magmas and mineralizing fluids of the Zinnwald tin-tungsten mining district, Erzgebirge, Germany},
  issn      = {0026-4598},
  year      = {2004},
  abstract  = {We remelted and analyzed crystallized silicate melt inclusions in quartz from a porphyritic albitezinnwaldite microgranite dike to determine the composition of highly evolved, shallowly intruded, Li- and F-rich granitic magma and to investigate the role of crystal fractionation and aqueous fluid exsolution in causing the extreme extent of magma differentiation. This dike is intimately associated with tin- and tungsten-mineralized granites of Zinnwald, Erzgebirge, Germany. Prior research on Zinnwald granite geochemistry was limited by the effects of strong and pervasive greisenization and alkali-feldspar metasomatism of the rocks. These melt inclusions, however, provide important new constraints on magmatic and mineralizing processes in Zinnwald magmas. The mildly peraluminous granitic melt inclusions are strongly depleted in CAFEMIC constituents (e.g., CaO, FeO, MgO, TiO2), highly enriched in lithophile trace elements, and highly but variably enriched in F and Cl. The melt inclusions contain up to several thousand ppm Cl and nearly 3 wt\% F, on average; several inclusions contain more than 5 wt\% F. The melt inclusions are geochemically similar to the corresponding whole-rock sample, except that the former contain much more F and less CaO, FeO, Zr, Nb, Sr, and Ba. The Sr and Ba abundances are very low implying the melt inclusions represent magma that was more evolved than that represented by the bulk rock. Relationships involving melt constituents reflect increasing lithophile-element and halogen abundances in residual melt with progressive magma differentiation. Modeling demonstrates that differentiation was dominated by crystal fractionation involving quartz and feldspar and significant quantities of topaz and F-rich zinnwaldite. The computed abundances of the latter phases greatly exceed their abundances in the rocks, suggesting that the residual melt was separated physically from phenocrysts during magma movement and evolution. Interactions of aqueous fluids with silicate melt were also critical to magma evolution. To better understand the role of halogen-charged, aqueous fluids in magmatic differentiation and in subsequent mineralization and metasomatism of the Zinnwald granites, Cl-partitioning experiments were conducted with a F-enriched silicate melt and aqueous fluids at 2,000 bar (200 MPa). The results of the experimentally determined partition coefficients for Cl and F, the compositions of fluid inclusions in quartz and other phenocrysts, and associated geochemical modeling point to an important role of magmatic-hydrothermal fluids in influencing magma geochemistry and evolution. The exsolution of halogen-charged fluids from the Li- and F- enriched Zinnwald granitic magma modified the Cl, alkali, and F contents of the residual melt, and may have also sequestered Li, Sri, and W from the melt. Many of these fluids contained strongly elevated F concentrations that were equivalent to or greater than their Cl abundances. The exsolution of F-, Cl-, Li-, +/- W- and Sn-bearing hydrothermal fluids from Zinnwald granite magmas was important in effecting the greisenizing and alkali-feldspathizing metasomatism of the granites and the concomitant mineralization},
  language  = {en}
}
@article{ForsterCooperRobertsetal.2003,
  author    = {Forster, Hans-J{\"u}rgen and Cooper, Mark A. and Roberts, Andrew C. and Stanley, Chris J. and Criddle, Alan J. and Hawthorne, Frank C. and Laflamme, J. H. Gilles and Tischendorf, Gerhard},
  title     = {Schlemaite, (Cu,square)(6)(Pb,Bi)Se-4, a new mineral species from Niederschlema-Alberoda, Erzgebirge, Germany : Description and crystal structure},
  year      = {2003},
  abstract  = {Schlemaite, with the simplified formula (Cu,rectangle)(6)(Pb,Bi)Se-4, is a new mineral species from the Niederschlema-Alberoda vein-type uranium deposit at Hartenstein, Erzgebirge, Germany. It occurs as anhedral to subhedral grains with no obvious forms or twinning, in aggregates of up to several hundred mum across, with berzelianite, eucairite and clausthalite in a dolomite-ankerite matrix. Schlemaite is black with a black streak and opaque with a metallic luster. It is brittle with an uneven fracture and no observable cleavage. It has a mean VHN (25 g load) of 106 kg/mm(2), which roughly equates to a Mobs hardness of 3. In plane-polarized reflected light, schlemaite is grey, non- pleochroic with a very weak bireflectance. It has very weak anisotropy, with rotation tints in shades of very pale metallic orange and blue, and shows no internal reflections. Electron-microprobe analyses yielded a mean composition Cu 38.86, Ag 2.57, An 0.07, Hg 0.09, Pb 13.75, Bi 9.12, Se 35.11, total 99.57 wt.\%. The empirical formula (based on 4 Se apfu) is (Cu5.50Ag0.21)(Sigma5.71)(Pb0.60Bi0.39)(Sigma0.99)Se-4. The calculated density is 7.54 g/cm(3) (based on the empirical formula and unit-cell parameters refined from single-crystal data). Schlemaite is monoclinic, P2(1)/m, a 9.5341(8), b 4.1004(3), c 10.2546(8) Angstrom, beta 100.066(2)degrees, V 394.72(9) Angstrom(3), a:b:c 2.3252:1:2.5009, Z = 2. The crystal structure of schlemaite was solved by direct methods and refined to an R index of 4.8\% using 1303 unique reflections collected on a four-circle diffractometer equipped with a CCD detector. The structure consists of intercalated ordered and disordered layers. The ordered layer consists of ladders of Ph2+ + Bi3+ coordinated by Se, the former showing strong lone-pair-stereoactive effects, and a network of Cu+ coordinated by Se anions. The disordered layer consists of an array of sites partly occupied by Cu+ and Ag+ in a variety of coordinations, and is characterized by strong short-range order. The strongest seven lines of the X-ray powder-diffraction pattern [d in Angstrom(I)(hkl)] are: 3.189(100)(012), 3.132(100)(112), 2.601(70)(113), 2.505(50)(311), 2.151(60)(014), 2.058(80)(020) and 1.909(50)(314). Although schlemaite is chemically similar to furutobeite, (Cu,Ag)(6)PbS4, it is not isostructural with it. The mineral is named after the Schlema-Alberoda uranium ore field near Schneeberg in the ancient mining region of Saxony, Germany},
  language  = {en}
}
@article{FoersterRomerGottesmannetal.2009,
  author    = {F{\"o}rster, Hans-J{\"u}rgen and Romer, Rolf L. and Gottesmann, B{\"a}rbel and Tischendorf, Gerhard and Rhede, Dieter},
  title     = {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},
  issn      = {0077-7757},
  doi       = {10.1127/0077-7757/2009/0138},
  year      = {2009},
  abstract  = {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.},
  language  = {en}
}
@article{KeutschFoersterStanleyetal.2009,
  author    = {Keutsch, Frank N. and F{\"o}rster, Hans-J{\"u}rgen and Stanley, Chris J. and Rhede, Dieter},
  title     = {The discreditation of hastite, the orthorhombic dimorph of CoSe2, and observations on trogtalite, cubic CoSe2, from the type locality},
  issn      = {0008-4476},
  doi       = {10.3749/canmin.47.4.969},
  year      = {2009},
  abstract  = {"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.},
  language  = {en}
}
@article{SeifertRhedeFoersteretal.2009,
  author    = {Seifert, Wolfgang and Rhede, Dieter and F{\"o}rster, Hans-J{\"u}rgen and Thomas, Rainer},
  title     = {Accessory minerals as fingerprints for the thermal history and geochronology of the Caledonian Rumburk granite},
  issn      = {0077-7757},
  doi       = {10.1127/0077-7757/2009/0147},
  year      = {2009},
  abstract  = {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.},
  language  = {en}
}