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ARCHIWUM MINERALOGICZNE

A JOURNAL OF GEOCHEMISTRY, MINERALOGY AND PETROLOGY
ESTABLISHED IN 1925 BY STANISLAW THUGUTT
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1993

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Note: below are given only the abstracts of the publications in vol. 49 no. 2, 1993. Any of the abstracts of the Symposium ECROFI XII and Session "Zinc and lead ore deposits - genetic problems"  published in vol. 49 no.1, 1993 of  "Archiwum Mineralogiczne" (total 117 items) is available by request as electronic or xerox copy from akozl@geo.uw.edu.pl. See Contents vol. 49 no. 1.

BAKUN-CZUBAROW, NONNA*; GAŁĄZKA-FRIEDMAN, JOLANTA**; SUWALSKI, JAN***; SZPILA, KAZIMIERZ****
*Institute of Geological Sciences, Polish Academy of Sciences, al. Żwirki i Wigury 93, 02-089 Warszawa, Poland; ** Institute of Physics, Warsaw University of Technology, Koszykowa 75, 00-662 Warszawa, Poland; ***Institute of Atomic Energy, Świerk, 05-400 Otwock, Poland; ****Institute of Geochemistry, Mineralogy and Petrography, Warsaw University, al. Żwirki i Wigury 93, 02-089 Warszawa, Poland
WEATHERING OF THE LOWER SILESIAN BASALTOIDS STUDIED BY MÖSSBAUER SPECTROSCOPY
Archiwum Mineralogiczne v. 49 no. 2 p. 3-21

The Fe3+/Fe2+ ratio seems to be the important index of the hypergenic alterations of the iron-rich igneous rocks, where various iron-bearing minerals are characterised by different iron oxidation states. Ten samples of the rocks from the Zaręba Górna quarry near Lubań, altered to different degrees, were selected to study the weathering processes of the Lower Silesian basaltoids. The Mössbauer spectra of the unaltered basaltoids consist of subspectra of olivine, pyroxenes and of Fe-Ti oxides. The Mössbauer spectrum of olivine containing Fe2+ forms the doublet characterized by isomer shift IS = 1.2 mm/s and quadrupole splitting QS = 3 mm/s. In the spectra of pyroxenes the ferric and ferrous doublets can be recognised. In the spectra of the most altered basaltoids the intensive doublet of smectite (IS = 0.35 mm/s and QS = 0.67 mm/s) as well as subspectra of the iron oxides can be seen. In the investigated weathering sequence of the basaltoids the Fe3+/Fe2+ ratios, as calculated from Mössbauer spectra, range from 0.52 to 2.34, while in the last three samples divalent iron has not been detected. Mössbauer spectrometry has proved to be a useful tool in studies of transformations of iron-bearing minerals as well as in investigations of iron migration in environments under variable physical and chemical conditions. In the studied rocks iron from the primary silicates and oxides migrated gradually into the secondary silicates and oxides. Iron shows also a tendency to migrate from silicate to oxide phases with increasing weathering. The Mössbauer technique can also be applied to identify iron-bearing minerals.
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BIAŁOWOLSKA, ANNA
Institute of Geochemistry, Mineralogy and Petrography, Warsaw University, al. Żwirki i Wigury 93, 02-089 Warszawa, Poland
ENCLAVES IN BASALTOIDS FROM THE ŁYSANKA AND TRUPIEŃ HILLS (LOWER SILESIA)
Archiwum Mineralogiczne v. 49 no. 2 p. 145-197

Basaltoids from the Łysanka and Trupień hills (Lower Silesia) have been studied as well as ultramafic and mafic enclaves present in them and pyroxene and olivine megacrysts. The enclaves in the mentioned basaltoids represent peridotites, pyroxenites and gabbroid rocks. The minerals of those rocks have undergone the following processes: recrystallisation, blastesis and melting in which intergranular solutions and metasomatic fluids have been significant. Due to the influence of these media there occurred a migration of many chemical elements, most important of them being calcium, chromium, aluminium and titanium. The enclaves of peridotites and green clinopyroxenites presumabły represent fragments of the matter from the upper mantle, while black clinopyroxenites from the enclaves are mainly cumulates. As it is supposed the early cumulates have undergone the process of gabbro formation which occurred in joint magma chambers. Megacrysts of pyroxenes and some olivine megacrysts have crystallised from the magmatic melt in the differentiated physico-chemical conditions. The peridotite enclaves in which the olivines have undergone a strong blastesis were a source for a majority of olivine megacrysts.
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GAWĘDA, ALEKSANDRA
Department of Earth Sciences, University of Silesia, Będzińska 60, 41-200 Sosnowiec, Poland
STRUCTURE, MINERAL COMPOSITION AND ORIGIN OF PEGMATITES FROM THE POLISH PART OF WESTERN TATRA MTS
Archiwum Mineralogiczne v. 49 no. 2 p. 113-144

This paper presents results of investigations of pegmatites from Polish part of the Western Tatra Mts. It was stated that the rocks under considerations were pure-line pegmatites. Their zonal structures were the results of a mineralogical succession and variability of the distribution and ratios of chemical components. There were distinguished two main mineral parageneses, caused probably with two generations of pegmatites with different relationships to the main deformational event and different crystallisation temperatures.
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GÓRECKA, EWA
Polish Geological Institute, Rakowiecka 4, 00-975 Warszawa, Poland
GENETIC MODEL OF Zn-Pb DEPOSIT IN THE OLKUSZ ORE DISTRICT (S POLAND)
Archiwum Mineralogiczne v. 49 no. 2 p. 23-80

General regularities of the formation of a Zn-Pb deposit in the Upper Devonian to Upper Jurassic carbonate sequence in the Olkusz ore district as well as the mineralogical and geochemical features are presented. Dynamics of the compressional, tensional and strike-slip structures influenced the flow of the mineralised fluids. Main ore bodies occur in tectonically downwarped areas formed by block faults of ledge character. Distinct cycles of the ZnS, PbS and FeS2 crystallisation were connected with pulsating inflow of the parent solutions. A genetic connection between the Zn-Pb ores hosted both by the Paleozoic and Mesozoic beds has been stated. The ore mineralisation probably developed during a relatively short time in the post-Jurassic age.

Blockdiagram presenting the distribution of the Zn-Pb ores in Mesozoic and Paleozoic beds
l -- Upper Devonian, 2 -- Lower Permian, 3 -- Lower Triassic, 4 -- Middle Triassic, 5 -- Upper Triassic, 6 -- Upper Jurassic, 7 -- Quaternary, 8 -- dislocation zone, 9 -- ore body, 10 -- ore zone, 11 -- presumed ore mineralization extent in Devonian beds.

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SŁABY, EWA
Institute of Geochemistry, Mineralogy and Petrology, University of Warsaw, al. Żwirki i Wigury 93, 02-089 Warszawa, Poland
MELTING OF ALKALI FELDSPARS -- A PROCESS CONTROLLED BY DIFFUSION?
Archiwum Mineralogiczne v. 49 no. 2 p. 99-111

Alkali feldspars from the xenoliths occurring in basanite are partły albitised microclines, annealed in the basanite melt. The annealing of the feldspars has caused their partial melting. The melting process has included mainly albite compounds of the previous microcline. Characteristic shape of the crystal-melt border and the diffusive alkali profiles on this border suggest that the microcline melting has been controlled by diffusion. Calculated time of the crystals melting indicates that the chemical equilibrium between crystal and melt has not been achieved.
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SZAMAŁEK, KRZYSZTOF*; BARCZUK, ANDRZEJ*; YOUSSEF, EL-SAYED A.A.**
*Warsaw University, Geological Faculty, al. Żwirki i Wigury 93, 02-089 Warszawa, Poland; **Cairo University, Geology Department, Faculty of Sciences, Giza, Egypt
GENESIS AND MINERALOGY OF LATERITIC KAOLIN AT ASWAN AREA (SW EGYPT)
Archiwum Mineralogiczne v. 49 no. 2 p. 81-97

Pisolitic kaolins from Central Wadi Kalabsha (southern Egypt) were studied to determine their mineralogy, internal structure of pisoids and the genetic process that led to their formation. Pisolites are present in varicoloured kaolins which are mainly composed of well crystalline kaolinite, additionally hematite, anatase and minor amounts oi Al-oxides (gibbsite, diaspore). On the basis of petrological and mineralogical studies different types of pisoids were determined. The oxygen/hydrogen isotopic ratio indicates that pisolitic kaolins were formed by lateritic weathering.
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WIERZCHOŁOWSKI, BOGUMIŁ
Institute of Geochemistry, Mineralogy and Petrography, Warsaw University, al. Żwirki i Wigury 93, 02-089 Warszawa, Poland
SYSTEMATIC POSITION AND GENESIS OF THE SUDETIC VOLCANIC ROCKS
Archiwum Mineralogiczne v. 49 no. 2 p. 199-235

The systematic position of the Sudetic volcanic rocks has been based on the chemical classification of the volcanic rocks TAS (Total Alkali-Silica) from 1989. According to that classification the Sudetic volcanic rocks are represented by basanites, tephrites, foidites (melanephelinites), picrobasalts, alkali basalts, medium- and high-potassium subalkaline basalts, hawaiites, mugearites, benmoreites, latites, high-potassium dacites, trachydacites, trachytes and high- and low-potassium rhyolites. The Cainozoic volcanic rocks (ultrabasic and basic) have been assigned to the group of the alkali olivine basalts of the continental type which are genetically related to the Central-European rift zone. Isotopic ratios of strontium and neodymium and the ratio of lanthanum vs niobium point to a mantle origin of the Cainozoic volcanic rocks. Magmas bearing some enclaves of the mantle peridotites, present in the volcanites, can be concemed as primary. The Lower Permian volcanic rocks have been assigned to a calcium-alkali sequence of the Andean type. Their origin can be considered in relation to two different magmas: the basic magma of the mantle origin and acid anatectic one.
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