Acta Mineralogica-Petrographica, Abstract Series 5, Szeged, 2006DISCRIM<strong>IN</strong>ATION BETWEEN TECTONIC ENVIRONMENTS OF OBSIDIAN SAMPLESUS<strong>IN</strong>G GEOCHEMICAL DATARÓZSA, P. 1 , SZÖŐR, GY. 1 , ELEKES, Z. 2 , GRATUZE, B. 3 , UZONYI, I. 2 & KISS, Á. Z. 21 Department of Mineralogy and Geology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, HungaryE-mail: rozsap@puma.unideb.hu2 Institute of Nuclear Research of the Hungarian Academy of Sciences [ATOMKI], Bem tér 18/C, H-4026 Debrecen, Hungary3 Centre de Recherches Ernest Babelon, CNRS, Orleans, FranceGeochemical analysis of obsidians is of great interest toarchaeometry. From the geological point of view, the importanceof elemental constituents of obsidians is that mineralogicalinformation can hardly be obtained on volcanicglasses. The non-destructive ion beam analysis (IBA) is suitablein general to determine major, minor and trace elementcontent; therefore, IBA methods are widely used in geoscienceresearch (RYAN, 2004), particularly in obsidianprovenance studies (see for example ELEKES et al., 2000).Obsidian samples from different localities of various geologicalsettings (Armenia, Hungary, Iceland, Mexico, Slovakia,Turkey) were analyzed by particle induced gamma-rayemission (PIGE) technique and laser ablation-inductivelycoupled plasma-mass spectrometry (LA-ICP-MS). Petrographically,all samples can be regarded as rhyolite accordingto their position in the TAS diagram. Classifying the studiedobsidian samples the R1–R2 diagram (DE LA ROCHE et al.,1980), where R1 = 4Si – 11(Na + K)–2(Fe + Ti) and R2 =6Ca + 2Mg + Al, was also applied. Although it is most usefuland generally used for plutonic rocks, the scheme is sufficientlygeneral to apply to volcanic rocks, too. Samples comingfrom Armenia and the Tokaj Mountains belong to rhyolites.Samples from the Lipari Islands and Turkey also fallinto this group, however their points are near the boundaryline separating the rhyolite and alkali rhyolite fields. However,points of the samples from Iceland and Mexico aresituated in the alkali rhyolite field as a consequence of theirhigher sodium and iron as well as lower calcium content.Obsidians are often classified chemically according to theirCaO, Al 2 O 3 as well as Na 2 O and K 2 O contents(MACDONALD et al., 1993). According to this characterization,all of the analyzed samples are subalkaline–peraluminous obsidians.Use of discrimination diagrams to classify granites accordingto their tectonic setting is common in the petrologicpractice. Applying the Ta–Yb and Nb–Y diagrams (PEARCEet al., 1984) it can be stated that samples from Hungarydominantly belonged to the field of volcanic-arc granites(VAG) as well as that of volcanic arc and syn-collisionalgranites (VAG + syn-COLG) as expected on the basis of theirtectonic setting. Position of samples from Turkey (syn-COLGand VAG + syn-COLG, respectively) also corresponds to theexpectations. Armenian obsidians are described as productsof a subduction related volcanic area. Their position in theNb-Y diagram corresponds to this fact; however, one samplecan be found in the field of within-plate granites (WPG) inthe Ta-Yb diagram. The sample from Lipari Islands alsobelongs to the WPG fields in both diagrams. On the otherhand, however, these samples are close to the dividing linebetween WPG as well as syn-COLG and VAG fields. Bothdiscrimination diagrams show the samples from Iceland andMexico to belong to the WPG field. This pattern may be inconnection with the alkaline character of the samples indicatedby the R1–R2 diagram.AcknowledgementsThis work has been supported by the Hungarian NationalScience Research Foundation (OTKA) under Research ContractNo. T046579.ReferencesDE LA ROCHE, H., LETERRIER, J., GRANDECLAUDE,P. & MARCHAL, M. (1980): Chemical Geology, 29:183–210.ELEKES, Z., UZONYI, I., GRATUZE, B., RÓZSA, P.,KISS, Á. Z. & SZÖŐR, GY. (2000): Nuclear Instrumentsand Methods in Physics Research B, 161/163: 836–841.MACDONALD, R., SMITH, R.L., & THOMAS, J. E.(1993): Chemistry of the subalkalic silicic obsidians. USGeological Survey Professional Paper, 1523. Washington:US Geological Survey.PEARCE, J. A., HARRIS, N. B. W. & T<strong>IN</strong>DLE, A. G.(1984): Journal of Petrology, 25: 956–983.RYAN, C. G. (2004): Nuclear Instruments and Methods inPhysics Research B, 219/220: 534–549.104www.sci.u-szeged.hu/asvanytan/acta.htm
Acta Mineralogica-Petrographica, Abstract Series 5, Szeged, 2006FERRUG<strong>IN</strong>OUS CONCENTRATIONS <strong>IN</strong> SANDSTONES NEAR DOBCZYCE (SILESIANUNIT, <strong>THE</strong> WESTERN POLISH <strong>CARPATHIANS</strong>) – PRELIM<strong>IN</strong>ARY RESULTSRZEPA, G., BAZARNIK, J., MUSZYŃSKI, M. & GAWEŁ, A.Department of Mineralogy, Petrography and Geochemistry, AGH University of Science and Technology, al. Mickiewicza 30,30-059 Krakow, PolandE-mail: grzesio@geolog.geol.agh.edu.plThe Istebna Beds that build the northern edge of theDobczyce retention reservoir on the Raba River near Brzączowice(ca. 30 km SE of Kraków) contain layers and bedsenriched in Fe compounds. They are rusty or yellowish, insome places become distinctly black. Within these iron-richhorizons, there occur characteristic, boxwork-like goethiteconcretions.Mineral composition of these ferruginous concentrationswith special attention to the boxwork-like concentrations,whose origin is still a matter of discussions, was investigatedusing transmitted light microscopy, X-ray diffractometry(XRD) and scanning electron microscopy (SEM-EDS). Theauthors also determined the contents of Fe and Mn; the figurescited below refer to the HCl-soluble Fe.Five types of Fe-rich concentrations that differ in theirmode of occurrence, Fe content and mineral compositionhave been distinguished on the basis of hand specimen featuresand preliminary mineralogical investigations:1) sandstones cemented (uniformly or non-uniformly) withFe oxyhydroxides (especially goethite), with coloursfrom yellow to almost black, containing dozen or so wt%Fe;2) goethite incrustations on the surfaces of sandstones,containing up to ca. 30 wt% Fe;3) boxwork-like concretions proper, composed almost ofpure goethite and containing up to 87 wt% Fe;4) sulphate-oxide concentrations, that are composed ofjarosite, goethite and detrital material and contain up to53 wt% Fe. Similar concentrations with secretion-likefeatures were described by GUCWA & WIESER (1976);5) phosphate-oxide aggregates that are mainly composed ofapatite, quartz, Fe and Mn oxides and contain up to 12wt% Fe.The main Fe mineral is usually cryptocrystalline goethite,but it may also form characteristic, fan-shaped aggregates ofelongated crystals, lining the walls of pores and fractures. Mnoxides are present in all types of ferruginous concentrations,either dispersed or in the form of incrustations, irregularconcentrations, veins and dendrites.On the basis of these preliminary investigations, the originof the Fe concentrations studied may be related to weatheringunder oxidizing conditions of primary, Fe-bearing minerals(silicates, sulphides and, possibly, carbonates) that musthave been present in surrounding rocks. Goethite, the mainFe component of these aggregates, can be formed in differentweathering environments characterized by a wide spectrumof physicochemical conditions (pH, Eh, foreign ions;CORNELL & SCHWERTMANN, 1996). Variations of theseparameters may have controlled the forms of occurrence andthe degree of crystallinity of goethite. Its presence in differentforms indicates several stages and/or mechanisms of weathering,various Fe sources, etc. The boxwork-like structuresresulted probably from precipitation of goethite from thesolutions that penetrated cracks in sandstones and progressivelyreplaced the primary rock with the iron oxyhydroxide(RUKH<strong>IN</strong>, 1953). In sulphate secretions goethite is probablya final product of co-existing jarosite transformation. Jarositecrystallizes from acid solutions with pH < 3 that are rich insulphates and Fe 3+ (DUTRIZAC & JAMBOR, 2000) and itspresence strongly implies weathering of sulphides.The investigations were supported by AGH-UST researchproject no. 11.11.140.158.ReferencesCORNELL, R. M. & SCHWERTMANN, U. (1996): Theiron oxides. Structures, properties, occurrences, characterizationand uses. Weinheim: VCH, 573 p.DUTRIZAC, J. E. & JAMBOR, J. L. (2000): In: ALPERS,C. N., JAMBOR, J. L. & NORDSTROM, D. K. (eds.)Sulfate minerals – crystallography, geochemistry and environmentalsignificance. Reviews in Mineralogy & Geochemistry,40: 405–452.GUCWA, I. & WIESER, T. (1976): Rocznik Polskiego TowarzystwaGeologicznego, 46: 197–215 (in Polish).RUKH<strong>IN</strong>, L. B. (1953): Osnovy litologii. Moskwa: Gostoptekhizdat,671 p. (in Russian).www.sci.u-szeged.hu/asvanytan/acta.htm 105
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