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PROGRAMME MinPet2009 & 4 th MSCC Joint Conference an “Eötvös Workshops in Science” meeting Budapest, Hungary, September 7—11, 2009 http://www.minpet2009mscc.org

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Page 1: PUBLIC LECTURE MinPet2009 & 4 MSCC · In this way the MinPet2009 & 4 th MSCC Joint Conference may become an important preparatory step of the IMA 2010 General Meeting (Budapest, August

PROGRAMME

MinPet2009 & 4thMSCCJoint Conferencean “Eötvös Workshops in Science” meeting

Budapest, Hungary, September 7—11, 2009http://www.minpet2009mscc.org

PUBLIC LECTURETuesday, September 8, 6 pm

Lecture room 0.823

MITT.ÖSTERR.MINER.GES. 156 (2010)

BIOMINERALS

Pósfai, M.

University of Pannonia, Veszprém, H-8200 Hungary

e-mail: [email protected]

Why are our bones strong and tough, why are our teeth hard? How do mussels and snails build their shells? Why can bacteria and birds navigate in magnetic fields? The lecture attempts to give answers to these questions: in all cases a biological function, such as support, protection or orientation, is served by composites of organic materials and inorganic crystals – biominerals – that form inside the living organism (MANN, 2001). The sizes, shapes, compositions, structures and arrangements of the mineral grains in the organism are all tightly controlled by various biological mechanisms that affect crystal nucleation and growth (Fig. 1). The highly constrained properties of biominerals distinguish them from their inorganically-formed counterparts. The study of biominerals uses research techniques and knowledge from several disciplines, including mineralogy, biology, physics, materials science and geology. In this lecture, we will employ a cross-disciplinary perspective to broadly review the functions, formation mechanisms and properties of biominerals.

Figure 1. Two pairs of chains of magnetite (Fe3O4) nanocrystals in the cell of a magnetotactic bacterium. The white lines represent a map of the magnetic induction, as obtained from electron holography in a transmission electron microscope, while the colours show the direction of the magnetic induction according to the colour wheel shown in the lower left. The highly constrained sizes, shapes and orientations of the ferrimagnetic nanocrystals result in a uniform magnetization along the chains, enabling the cell to swim parallel to the Earth’s magnetic field. Figure adapted from SIMPSON et al. (2005).

MANN, S. (2001): Biomineralization: Principles and concepts in bioinorganic materials chemistry. Oxford University Press, Oxford, 198 pp. SIMPSON, E.T., KASAMA, T., PÓSFAI, M., BUSECK P.R., HARRISON, R.J., DUNIN-BORKOWSKI, R.E. (2005): J. Phys. Conf. Ser., 17, 108-121.

Page 2: PUBLIC LECTURE MinPet2009 & 4 MSCC · In this way the MinPet2009 & 4 th MSCC Joint Conference may become an important preparatory step of the IMA 2010 General Meeting (Budapest, August

0.823K itaibelRoom

BASEMENT

DA

NU

BE

N

SPosters(aula)

BiologicalExhibition

Historical Mineral Hall

0.823KitaibelRoom

Room

0-822

Entrance II (N)

DA

NU

BE

N

S

Posters(aula)

BiologicalExhibition

Room

0-823

Room

0-803

Room

0-804

Room

0-822

Room

0-823

Room

0-804Room

0-803

Registration

S0-721

Ladies ’r oom

Men’s room

SSpeakers’ room(0-721)

Entrance

C

C Cloakroom

M

M

M M

M

Eötvös Loránd University, Riverside Campus, Building C1117 Budapest, Pázmány Péter sétány 1/C

GROUND FLOOR

Entrance I (W)Entrance III (E)

(Danube entrance)

Dept. of Mineralogy

Monday, September 713:00—20:00 Registration, mounting of posters / Field trip 1 13:00—20:0019:30—21:30 Ice breaker party 19:30—21:30

Tuesday, September 8 8:00—8:50 Registration, mounting of posters 8:00—8:50 9:00 Opening 9:00 9:15

Plenary lecturesPL1: Luttge 9:15

9:45 PL2: Robert 9:4510:15 Coffee/posters 10:1511:00

Crystallography

1A1: Amthauer

Geochemistry-Petrology 1

1B1: Koller 11:0011:20 1A2: Miletich 1B2: Kiss G. 11:2011:40 1A3: Talla 1B3: Beqiraj 11:4012:00 1A4: Arroyabe 1B4: Prechtel 12:0012:20 Lunchbreak 12:20

14:00POSTER DISCUSSION 1

coffee/beer14:00

16:00

Applied,environmental,and claymineralogy

1A5: Kaindl

Geochemistry-Petrology 2

1B5: Demény 16:0016:20 1A6: Klimko 1B6: Coban 16:2016:40 1A7: Bolanz 1B7: Karaoglan 16:4017:00 1A8: Rostási 1B8: Jankovics 17:0017:20 1A9: Diekamp 1B9: Kiss B. 17:2017:40 1A10: Mittermayr 1B10: Moazzen 17:4018:00—18:45 Public lecture PU1: Pósfai 18:00—18:45

Wednesday, September 9 8:30

Mineral deposits

2A1: Mogessie

Geochemistry-Petrology 3

2B1: Bruand 8:30 8:50 2A2: Aiglsperger 2B2: Klötzli 8:50 9:10 2A3: Földessy 2B3: Dégi 9:10 9:30 2A4: Azim Zadeh 2B4: Németh 9:30 9:50 2A5: Gál 2B5: Tropper 9:5010:10 Coffee/posters 10:1010:40

Generalmineralogy, Archaeometry

2A6: Çina

Geochemistry-Petrology 4

2B6: Buda 10:4011:00 2A7: Kristály 2B7: Broska 11:0011:20 2A8: Bačík 2B8: Kurt 11:2011:40 2A9: Jáger 2B9: Petrík 11:4012:00 2A10: Ionescu 2B10: Göd 12:0013:00—19:00 Field trip 2 Dunabogdány 13:00—19:0020:00 Conference dinner 20:00

Thursday, September 10 9:00

Plenary lecturesPL3: Armbruster 9:00

9:30 PL4: Dódony 9:3010:00 Coffee/posters 10:0010:30

Generalmineralogy,Teaching

3A1: Nasdala

Geochemistry-Petrology 5

3B1: Vető 10:3010:50 3A2: Uher 3B2: Höllen 10:5011:10 3A3: Ondrejka 3B3: Puhr 11:1011:30 3A4: Ertl 3B4: Sági 11:3011:50 3A5: Chudik 3B5: Klébesz 11:5012:10 3A6: Farkas 3B6: Shafaii 12:1012:30 3A7: Viczián 12:3012:50 Lunchbreak 12:50

14:30POSTER DISCUSSION 2

coffee/beer14:30

17:00 Plenary lecture PL5: Stalder 17:0017:30—17:45 Closing 17:30—17:4518:00 IMA2010 CRT meeting 18:00

Friday, September 11Field trip 3

Page 3: PUBLIC LECTURE MinPet2009 & 4 MSCC · In this way the MinPet2009 & 4 th MSCC Joint Conference may become an important preparatory step of the IMA 2010 General Meeting (Budapest, August

MinPet2009 & 4th Mineral Sciences in the Carpathians Joint Conference

an Eötvös Workshops in Science meeting

Budapest, Hungary, September 7–11, 2009

Programme

ORGANISERSMineralogical Society of Austria (ÖMG)

Mineralogical-Geochemical Branch of the Hungarian Geological Society (MFT)Faculty of Science, Eötvös Loránd University (ELTE TTK)

CO-ORGANISERS

Croatian Mineralogical AssociationCzech Geological Society

Mineralogical Society of PolandMineralogical Society of Romania

Mineralogical-Geochemical Branch of the Geological Society of Slovakia Ukrainian Mineralogical Society

Page 4: PUBLIC LECTURE MinPet2009 & 4 MSCC · In this way the MinPet2009 & 4 th MSCC Joint Conference may become an important preparatory step of the IMA 2010 General Meeting (Budapest, August

REPRESENTATIVES OF THE ORGANISING BODIES ÖMG: Richard Göd, Friedrich KollerMFT: Tamás G. Weiszburg, Gábor PappELTE TTK: István Dódony, György Lovas, Erzsébet Tóth

CO-ORGANISING BOARD

V. Bermanec (HR), I. Broska (SK), M. Chovan (SK), G. Ilinca (RO), C. Ionescu (RO),V. Kvasnytsya (UA), M. Michalik (PL), M. Novák (CZ), D. Tibljas (HR)

ADDRESS FOR CORRESPONDENCE AND INFORMATION

MinPet2009MSCC c/o Department of Mineralogy, Eötvös L. UniversityH-1117 Budapest HungaryPhone: +36-1-3812205Fax: +36-1-3812110Homepage: http://www.minpet2009mscc.org

CONTACT PERSONS LOCAL ORGANISING COMMITTEE:Tamás G. Weiszburg ([email protected]) István Dódony ([email protected])

PUBLICATION SUBCOMMITTEE:Gábor Papp ([email protected])Richard Tessadri ([email protected])

LOCAL ORGANISING COMMITTEE

D. Breitner, I. Cora, A. Demény, I. Dódony, Sz. Harangi, R. Hohol, M. Jánosi, P. Kónya, I. Kovács,Gy. A. Lovas, G. Papp, I. Márton, F. Molnár, Cs. Szabó, V. Szilágyi, E. Tóth, T. G. Weiszburg

SCIENTIFIC SPONSORS

• Faculty of Science, Eötvös Loránd University (ELTE)• Department of Mineralogy and Petrology, Hungarian Natural History Museum• Institute for Geochemical Research of the Hungarian Academy of Science• Committee on Geochemistry, Mineralogy and Petrology, Section of Earth Sciences,

Hungarian Academy of Science• International Year of Planet Earth Hungarian National Committee

Established by the support of the National Office for Research and Technology.

Albert programmeApponyiMEC

Page 5: PUBLIC LECTURE MinPet2009 & 4 MSCC · In this way the MinPet2009 & 4 th MSCC Joint Conference may become an important preparatory step of the IMA 2010 General Meeting (Budapest, August

Contents

WELCOME TO CONFERENCE PARTICIPANTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

PROGRAMME . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5Brief summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Thematic overview, locations and practical information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

LIST OF ACCEPTED PRESENTATIONS BY SESSIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7Invited plenary lectures (PL) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Invited public lecture (PU) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

General mineralogy (GEN) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Crystallography (CRY) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

Petrology (PET) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8

Geochemistry (GCH) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

Mineral deposits (DEP) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

Applied, environmental and clay mineralogy (AEC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

Archaeometry / science history (ARC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

ABSTRACTS OF INVITED PLENARY LECTURES (IN CHRONOLOGICAL ORDER) . . . . . . . . . . . . . . 14

Luttge, A. & Arvidson, R.S.: Contours of a new theory on crystal dissolution . . . . . . . . . . . . 14 (A1)

Robert, J.-L.: Crystal chemistry of light elements in major rock-forming minerals . . . . . . . . 15 (A2)Armbruster, T.: Magnesium phosphates: From molecular structures to stronglycondensed minerals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 (A3)

Dódony, I.: Cation ordering in silicates as shown by electron crystallography . . . . . . . . . . . . 17 (A4)

Stalder, R.: Hydrous defects in pyroxenes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 (A5)

ABSTRACTS TO BE PUBLISHED IN MITT. ÖSTER. MINER. GES., 156 (2010)(IN ALPHABETICAL ORDER) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

Cora, I. & Weiszburg, T. G: Nano-sized mineralogy of a Toarcian manganese deposit(Úrkút, Hungary) and the importance of Mn3+ in its genesis . . . . . . . . . . . . . . . . . . . . . . . . . . 19 (A6)Menyhárt, A., Dódony, I. & Pekker, P.: New mineralogical data from the environsof Mád, Tokaj Mts., Hungary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 (A7)Nasdala, L., Grötzschel, R., Probst, S., Ruschel, K. & Hanchar, J.M.: Irradiation damagein monazite: A Raman study of Au-irradiated FIB foils . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 (A8)Pekker, P., Dódony, I. & Weiszburg, T. G.: TEM study of amorphous iron oxideprecipitates from the Mátraszentimre Pb-Zn ore mine, Mátra Mts., Hungary . . . . . . . . . . . . . 22 (A9)

Szabó, B. & Weiszburg, T. G.: Mineralogical examination of hazardous wastes . . . . . . . . . . 23 (A10)Szilágyi, V., Gál-Mlakár, V., Rácz, T.Á., Sajó, I. & Simonyi, E.: First results of thearchaeometric investigation of the Buda white ware (12th–15th century, North Hungary) . . . . 24 (A11)

INDEX OF AUTHORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

MAP OF THE RIVERSIDE CAMPUS OF THE EÖTVÖS LORÁND UNIVERSITY (ELTE)AND ITS SURROUNDINGS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

On the inside cover: Programme at a glance On the inside back cover: Map of the Conference area, Building C, ELTE Riverside CampusPhoto on the cover (Historical Mineral Hall of the Eötvös Museum of Natural History) by Péter Pekker

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Welcome to Conference Participants

The organising societies and the organising committee warmly welcome the participants of the MinPet2009 & 4th Mineral Sciences in the Carpathians Conference, the joint meeting of two traditional meeting series (the biennial MinPet and the triennial MSCC). Some 170 colleagues from 17 countries of Europe and beyond registered at the meeting. Most of the participants of the conference are, as a matter of course, from the countries of the Alpine–Carpathian–Pannonian Region. Therefore, our assembly is well aware that, as the invitation formulated, from mineralogical and geochemical points of view this region is among the most interesting and complex areas of Europe. It is to be hoped that the present meeting, by giving an insight in the state of art of mineral sciences in the region, will help colleagues working in other parts of the world to realise this uniqueness. In this way the MinPet2009 & 4th MSCC Joint Conference may become an important preparatory step of the IMA 2010 General Meeting (Budapest, August 2010), the quadrennial world conference now jointly organised by the countries of the Alpine-Carpathian-Pannonian Region.

SCIENTIFIC PROGRAMME

The scientific programme covers mineralogy, geochemistry, crystallography, petrology and mineral deposits, as well as their applications, with special emphasis on the broad sense Alpine–Carpathian–Pannonian Region. Some 60 contributions are presented in the oral and 110 in the poster sessions, fruits of the research activity of some 380 authors and co-authors altogether. Five plenary presentations report exciting new results from different fields of our science. A public lecture on the emerging research field of biominerals is intended to attract audience from all disciplines of science.

VENUE

The Conference is held at the Danube Riverside Campus of the Eötvös Loránd University, Building C (see p. 28 for the campus map and the opposite inside back cover page for a map of the conference area within Building C).

Department of Mineralogy, Eötvös Loránd University, has proved to be a well-tried venue of several scien-tific meetings in the past 15 years. The Eötvös University, celebrating the 235th anniversary of its organised min-eralogical education and the 160th anniversary of the founding of the independent Department of Mineralogy, offers a friendly environment also for the current conference. Participants will have the opportunity to visit the 235-year-old Mineral Collection (saved in its historical 19th century form), venue for the ice breaking party.

The Danube Riverside Campus of the Eötvös University is close to the heart of Budapest. Architectural monuments, museums, shops are easy to reach from here. A week in Budapest may give a pleasant tourist experience also to the accompanying guests.

SEE YOU AGAIN AT IMA 2010!

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Programme

BRIEF SUMMARY (see inside cover for a detailed, tabulated overview)

Sunday (Sept. 6): arrivals and early registration for participants of Field trip 1 (starting from Budapest)

Monday (Sept. 7): one day field trip (Field trip 1), for registered participants, starting both from Vienna and Budapest) to the Balaton Highland; arrivals, registration; evening: icebreaker party.

Tuesday (Sept. 8): full day scientific sessions

Wednesday (Sept. 9): morning: scientific sessions, afternoon: Field trip 2 for registered participants to Dunabogdány; and the Danube Bend. Evening: Conference dinner (optional).

Thursday: (Sept. 10): full day scientific sessions

Friday: (Sept. 11): one day field trip (Field trip 3) for registered participants to the Bükk Mts. (NE Hungary) ending in Budapest in the late evening hours.

THEMATIC OVERVIEW, LOCATIONS AND PRACTICAL INFORMATION

Registration deskRegistration desk is open from September 7, (Monday) 1 pm till September 10 (Thursday) 6 pm, during the conference activities, in the area of the Department of Mineralogy (Building C, see ground floor map on inside back cover for location)

OPENING AND CLOSING EVENT, PLENARY AND PUBLIC LECTURES

Opening sessionSeptember 8 (Tuesday), 9 am, Room 0-823György Michaletzky (Dean of the Faculty of Science, Eötvös Loránd University, Budapest)Richard Göd (President of the Austrian Mineralogical Society)János Haas (President of the Hungarian Geological Society)

Plenary lectures (see pages A1–A5 for the abstracts) Room 0-823

PL1: Contours of a new theory on crystal dissolution by Andreas Luttge, September 8 (Tuesday), 9:15 am

PL2: Crystal chemistry of light elements in major rock-forming minerals by Jean-Louis Robert, September 8 (Tuesday), 9:45 am

PL3: Magnesium phosphates: From molecular structures to strongly condensed minerals by Thomas Armbruster, September 10 (Thursday), 9 am

PL4: Cation ordering in silicates as shown by electron crystallography by István Dódony, September 10 (Thursday), 9:30 am

PL5: Hydrous defects in pyroxenes by Roland Stalder, September 8 (Tuesday), 5 pm

Public lecture (see back cover for the abstract) Room 0-823PU1: Biominerals by Mihály Pósfai: September 8 (Tuesday), 6 pm

Closing sessionSeptember 10 (Thursday), 5:30 pm, Room 0-823Ekkehart Tillmanns (Chairman of the Scientific Programme Committee, IMA2010)Tamás G. Weiszburg (Chairman of the Organising Committee, IMA2010)

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ORAL PRESENTATIONS

The non-plenary oral presentations run concurrently in two parallel sessions. Room A (Rooms 0-823, respectively 0-822): mineralogy-related presentations, Room B (Rooms 0-803, respectively 0-804): geochemistry-petrology-related presentations. (See inside cover for a detailed, tabulated overview)

Length of the oral presentations: 20 minutes (15 minutes talk + 5 minutes discussion)

Uploading time: Uploading talks from a USB stick or CD is suggested to be completed on the day prior to the talk in the speakers’ room (see map on inside back cover). Late speakers can upload their files directly in the lecture room the latest 20 minutes before the start of the session. (A technician will be present in the room.)

Notes:1) Presentations containing special features (movies, animations etc.) should be checked due time prior to the session.2) Speakers wishing to present their talks from their own Apple Computer should ensure that their machine has got the

appropriate VGA connector and it will work appropriately with the data projector at the conference site.3) Unless special technical conditions require, it is not possible to present talks using a speaker’s PC laptop, as this

disrupts the smooth running of the session.

POSTER PRESENTATIONS (see map on inside back cover for location)

Posters can be put up on the assigned board during the registration period: Monday, 1 pm – 9 pm and Tuesday 8 am – 8:45 am. Posters will be on display during the whole conference and should be removed on Thursday 4:50 pm – 6:30 pm.

Posters are arranged by sessions, see pp. 7–13 for your poster code. Pins to attach posters to the board will be supplied.

All breaks and the two dedicated poster sessions (with no concurrent oral session, September 8, Tuesday, 2 pm – 4 pm and September 10, Thursday, 2:30 pm – 5 pm) can be used for poster discussion. Poster presenters are expected to indicate their presence at their poster on the time table provided by the organisers to each poster board right after mounting of the posters.

SOCIAL EVENTS

Icebreaker party (for every participant), September 7 (Monday), 7:30 pm – 9:30 pm Historical Mineral Hall of the Eötvös Museum of Natural History (access through the Department of Mineralogy, see map on inside back cover)

Conference dinner (included in full registration fee only; further tickets in limited number can be bought at the registration desk), September 9 (Wednesday), 8:00 pmHotel Gellért, Panorama Restaurant1111 Budapest, Szent Gellért tér 1. (Buses 7, 86, 173, trams 18, 19, 41, 47, 49, 61)

REFRESHMENTS, MEALS

Refreshments and snacks will be served in breaks and during the two poster sessions. Fast food facilities in the neighborhood of the campus are shown on the map on page 28 (opposite to inside back cover).Ladies’ and Men’s rooms, Cloakroom see map on inside back cover.

FIELD TRIPS (for registered participants only)

FT1 (Balaton Highland): practical information was sent directly to participantsFT2 (Dunabogdány and Danube Bend): Departure: September 9 (Wednesday), 1 pm, Building C, Danube

entrance (see map) FT3 (Bükk Mts.): practical information was sent directly to participants

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List of accepted presentations by sessions

This table contains the accepted presentations of the MinPet2009 & 4th MSCC Joint Conference, arranged by sessions. In each session oral (O) and poster (P) presentations are listed separately, in alphabetical order. Number in the “page” column corresponds to the page number of the Mitteilungen der Österreichischen Mineralogischen Gesellschaft, Vol. 155, 2009, containing the relevant abstract. Number starting with A corresponds to the page number of the abstract pages in this programme booklet. (Top of the page, above the line near the spine.) The alphanumeric code in the last column corresponds to

i) for oral presentations: the day (1: September 8, Tuesday, 2: September 9, Wednesday, 3: September 10, Thursday), the lecture room (Room A or B), and the sequential number of the lecture (see the tabulated programme on the inside cover);

ii) for poster presentations: the code on the stand in the poster area.

INVITED PLENARY LECTURES (PL)

presenting author title of presentation page code

1 O ARMBRUSTER, Thomas Magnesium phosphates: From molecular structures to strongly condensed minerals

22 (A3) PL3

2 O DÓDONY, István Cation ordering in silicates as shown by electron crystallography A4 PL4

3 O LUTTGE, Andreas Contours of a new theory on crystal dissolution 96 (A1) PL1

4 O ROBERT, Jean-Louis Crystal chemistry of light elements in major rock-forming minerals A2 PL2

6 O STALDER, Roland Hydrous defects in pyroxenes 147 (A5) PL5

INVITED PUBLIC LECTURE (PU)

presenting author title of presentation page code

1 O PÓSFAI, Mihály Biominerals programmeback cover

PU1

GENERAL MINERALOGY (GEN)

presenting author title of presentation page code

1 O BAČÍK, Peter Mukhinite, “tawmawite” and dissakisite: Crystal chemistry of the V-, Cr- and REE-rich epidote-group minerals

28 2A8

2 O CHUDÍK, Peter Nb-Ta oxide minerals from the Jezuitské Lesy granitic pegmatite, Bratislava Massif, Western Carpathians, Slovakia: Compositional variations and evolution

40 3A5

3 O ÇINA, Aleksander Ni-rich cobaltite-nickeline and cobaltite-alloclasite assemblages from ophiolite complex of Albania

42 2A6

4 O ERTL, Andreas The schorl-elbaite solid solution and useful correlations 55 3A4

5 O JÁGER, Viktor Lower Cretaceous continental rift-type black smoker system in the East Mecsek Mts.

70 2A9

6 O KRISTÁLY, Ferenc Regional distribution of As-minerals in the Neogene volcanic arc– Cretaceous flysch boundary in the Romanian East Carpathians

94 2A7

7 O NASDALA, Lutz Irradiation damage in monazite: A Raman study of Au-irradiated FIB foils

A8 3A1

8 O ONDREJKA, Martin Sulfur in monazite: a “clinoanhydrite” substitution mechanism in natural occurrences and their genetic significance

118 3A3

9 O UHER, Pavel Accessory rare-element (REE, Y, Zr, Th, Nb, Ta) minerals of the Turčok A-type metagranite, Gemeric Unit, Slovakia: Tracers of magmatic to metamorphic evolution

166 3A2

1 P ATANASSOVA,Radostina G.

Natural dissolution features of sulphides from Madan Pb-Zn ore deposits, South Bulgaria

24 GEN01

2 P BATKI, Anikó Calcic to sodic-calcic amphiboles of lamprophyres from the Ditrău Alkaline Massif

29 GEN02

3 P DRÁBEK, Milan The Fe-Mo-Nb-S system: Phase relations of edgarite 53 GEN03

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GENERAL MINERALOGY (GEN) – continued

presenting author title of presentation page code

4 P GRECHANOVSKAYA, Elena E.

Structural state and genesis of adularia from ignimbrites of Sokyrnitsya deposit (Transcarpathians, Ukraine)

99

5 P IONESCU, Corina New data on the Sopot chondritic meteorite (Romania): Comparative electron microprobe and Raman study

68 GEN05

6 P KÓNYA, Péter New cavity filling zeolites from the basalts of the Bakony-Balaton Highland Volcanic Field (Western Hungary)

87 GEN06

7 P KOVÁCS-PÁLFFY, Péter Re-examination of “monsmedite” from the type locality, Baia Sprie, Baia Mare District (Romania)

88 GEN07

8 P MENYHÁRT, Adrienn New mineralogical data from the environs of Mád, Tokaj Mts., Hungary A7 GEN08

9 P MESIARKINOVÁ,Martina

Study of hydrothermal SiO2 mineralization on the locality Ľubietová

- Jamešná (Slovakia)101 GEN09

10 P MIRON, Dan G. Zeolite mineralization in the Jurassic island arc volcanics from South Apuseni Mountains

103 GEN10

11 P MIRWALD, Peter P-T-stability of silver oxalate and the melting curve of CO2

104 GEN11

12 P NASDALA, Lutz Photoluminescence emission of Rare Earth Elements in natural monazite and synthetic orthophosphates

112 GEN12

13 P RUSCHEL, Katja Effect of fluid-driven chemical alteration on radiation-damaged fergusonite

138 GEN13

14 P TROPPER, Peter The most P-rich olivine on Earth so far: The formation of extremely phosphorous olivine in prehistoric burning slags from the Goldbichl, Igls (Tyrol, Austria)

142 GEN14

15 P TROPPER, Peter Biotite und apatite compositions as petrogenetic indicators in magmatic rocks from the Athesian Volcanic Group (South Tyrol, Italy)

144 GEN15

16 P VÁCZI, Tamás Decomposition textures after dry thermal annealing of zircon 167 GEN16

CRYSTALLOGRAPHY (CRY)

presenting author title of presentation page code

1 O AMTHAUER, Georg Electronic and magnetic structure of pyroxenes I. Hedenbergite 62 1A1

2 O ARROYABE, Erik K2Ca

4Si

8O

21 – An unusual layer silicate containing Q2 and Q3 units 23 1A4

3 O MILETICH, Ronald Heavy-ion irradiation and its consequence on the elastic properties of cordierite

102 1A2

4 O TALLA, Dominik Traces of structural H2O molecules in barite 158 1A3

1 P BOTTA, Claudio Structural investigations on a sulphate apatite 36 CRY01

2 P GIESTER, Gerald Crystal structure of nanlingite – The first mineral with a [Fe(AsO3)

6]

configuration177 CRY02

3 P KOLITSCH, Uwe An orthorhombic dimorph of barstowite, Pb4Cl

6(CO

3).H

2O, from slags at

Maria Waitschach, Austria, and Lavrion, Greece83 CRY03

4 P NYÍRÔ-KÓSA, Ilona Structures and compositions of maghemite nanoparticles 117 CRY04

5 P ORBÁN, Richárd Kaolinite polytypes 120 CRY05

6 P PEKKER, Péter TEM study of amorphous iron oxide precipitates from the Mátraszentimre Pb-Zn ore mine, Mátra Mts., Hungary

A9 CRY06

7 P PRISTACZ, Helmut Crystal structure of CaSeO4 and its relationship to anhydrite 133 CRY07

8 P SAGL, Raffaela High-pressure behaviour of realgar 140 CRY08

9 P TILLMANNS, Ekkehart Flux growth and topologies of three new complex silicates of gadolinium 176 CRY09

PETROLOGY (PET)

presenting author title of presentation page code

1 O BROSKA, Igor Fe-Ti oxides of West Carpathian granitoids: Indicators of mixing processes and a tool for regional granite mapping

37 2B7

2 O BRUAND, Emilie Pseudosection modelling of a low-Mg eclogite from the type locality (Koralpe, Eastern Alps)

38 2B1

3 O BUDA, György Two main types of Variscan granitoids in the Tisia Composite Terrane (Hungary)

39 2B6

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9

PETROLOGY (PET) – continued

presenting author title of presentation page code

4 O COBAN, Hakan Quartz-bearing basalts from Karadag stratovolcano, Central Anatolian extensional setting: Oxygen isotopic evidence for crustal contamination

43 1B6

5 O DÉGI, Júlia Crustal thickening during the Alpine orogeny: Insights from mafic granulite xenoliths of the Pannonian Basin

47 2B3

6 O JANKOVICS, Éva An insight in the depth: Petrogenesis of the basalt of the Füzes-tó scoria cone

71 1B8

7 O KISS, Balázs Magma chamber processes and magma ascent rate beneath the Ciomadul Mic (Kis-Csomád) lava dome

76 1B9

8 O KLÖTZLI, Urs S. Depicting time scales in the formation of the lower continental crust of the Ivrea-Verbano Zone (North Italy)

82 2B2

9 O KOLLER, Friedrich Contrasting mantle section in Albanian ophiolites: Evidences from mineral and bulk rock composition

84 1B1

10 O KURT, Hüseyin Petrogenesis of the Üçkapili granitoid and its mafic enclaves in Elmali area (Nigde, Central Anatolia)

95 2B8

11 O MOAZZEN, Mohssen Mineralogy and geochemistry of metabasic rocks from the Khoy area, NW Iran

107 1B10

12 O NÉMETH, Bianca Mid-crustal felsic granulite xenoliths from the Western Pannonian Basin (Beistein, Austria)

115 2B4

13 O PETRÍK, Igor Rare phosphates from a Li-F-P granite (Gemeric Unit, Western Carpathians, Slovakia)

127 2B9

14 O PRECHTEL, Felix Defect distribution in orthopyroxene at elevated pressures 132 1B4

15 O PUHR, Barbara Petrology of metacarbonate rocks of the Austroalpine Basement east of the Tauern Window (Austria)

134 3B3

16 O SHAFAII MOGHADAM, Hadi

Post-collisional calc-alkaline to shoshonitic volcanism in NW of Iran: Constraints from geochemistry and petrogenesis

145 3B6

17 O TROPPER, Peter Salt matters: Experimental investigations of the transformation of high-grade metapelites and granites to eclogites and the role of brines in subduction zone processes

164 2B5

1 P ABU-ALAM, Tamer Sabry The MBC(1.7)

: A Visual Basic program to calculate bulk composition of rocks from chemistry and the volume proportions of the phases

17 PET01

2 P ABU-ALAM, Tamer Sabry Fluid infiltration and metasomatism processes in Wadi Solaf calc-silicate, Egypt

18 PET02

3 P ABU-ALAM, Tamer Sabry The Feiran metamorphic complex of Sinai: Its relationship to the core complexes of the Arabian Nubian Shield

19 PET03

4 P COBAN, Hakan Oxygen and strontium isotopic evidence for the effect of carbonate metasomatism on the genesis of inner Isparta angle potassic volcanism, SW Anatolia

44 PET04

5 P ČOPJAKOVÁ, Renata Clasts of Variscan rocks within the Kořenec and Račice conglomerates (Rhenohercynicum, Bohemian Massif), Th-U-total Pb evidence from an electron microprobe monazite study

45 PET05

6 P GHORBANI, Ghasem Geochemistry of Paleozoic basaltic rocks from north of Shahrood, N Iran 61 PET06

7 P HAUZENBERGER, Christoph A.

New U-Pb zircon age constraints on the magmatic and metamorphic evolution of granulite facies basement rock from Southern Tanzania

63 PET07

8 P HIDAS, Károly Petrologic and geochemical study on sulfide melt inclusions hosted by upper mantle xenoliths from alkali lamprophyres (Tuva, S Siberia, Russia)

85 PET08

9 P HOLZMANN, Jan Petrology of the contact between the lithologies of the Pb-Zn ore deposits Pflersch Valley - Schneeberg (South Tyrol, Italy) and its polymetamorphic host rocks

66 PET09

10 P KONRAD, Lukas Petrology and geochemistry of mantle xenoliths from Lethlakane, Botswana and from Kimberley area, South Africa

186 PET10

11 P KOZLIK, Michael Titanite zoning as a recorder of the metamorphic evolution of metacarbonates from the central Oetztal Complex (North Tyrol, Austria)

89 PET11

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10

PETROLOGY (PET) – contimued

presenting author title of presentation page code

12 P KRENN, Kurt HP-fluid inclusions in tourmaline, apatite and quartz from eclogites of the Austroalpine Polinik Complex (Kreuzeck Mountains, Eastern Alps)

90 PET12

13 P MELNIKOV, Vladimir S. Immiscibility in rhyolite-dacitic magma fixed in ignimbrites of Sokyrnitsya deposit (Transcarpathians, Ukraine)

100 PET13

14 P MOLNÁR, Ferenc Partial melting and melt segregation in footwall units within the contact aureole of the Sudbury Igneous Complex (North and East Ranges, Sudbury structure, Ontario, Canada)

124 PET14

15 P NANTASIN, Prayath Petrography and mineral chemistry of the Thab Sila Gneiss, Kanchanaburi Province, Western Thailand

111 PET15

16 P NÉDLI, Zsuzsanna Evolution of the pre-Neogene subcontinental lithospheric mantle beneath the Poiana Ruscă Mts. (W Romania)

114 PET16

17 P PINTÉR, Zsanett Petrographic and fluid inclusion study of upper mantle xenoliths from the Cameroon volcanic line

128 PET17

18 P ROFNER, Verena The petrology of an amphibolite-metagabbro complex and hornfelses from the Southalpine basement in the northern Eisack Valley (Gufidaun, South Tyrol, Italy)

136 PET18

19 P SCHEIPL, Gregor New geochronological data from rocks of the Bulgarian Rhodope 141 PET19

20 P STEIDL, Magdalena Petrology of metapelites from the Michelbach Complex (Defereggen Complex, Eastern Tyrol)

149 PET20

21 P STÖBICH, Eva The search for Early Variscan high-P metamorphism in the Moldanubian: Thermobarometry of granulites from the Bavarian Forest, Southern Bohemian Massif, Bavaria

150 PET21

22 P SZABÓ, Ábel Metasomatic imprints below the Eastern Transylvanian Basin – amphiboles in the upper mantle xenoliths

155 PET22

23 P TAFERNER, Harald Occurrence of chrome-kyanite in eclogites from Pohorje, Slovenia 156 PET23

24 P TRIBUS, Martina Apatite as a monitor of trace element variations in a contact aureole: Combining experimental and petrological investigations from the Brixen granite contact aureole

162 PET24

25 P TROPPER, Peter Solubility of accessory minerals (CePO4, YPO

4) in H

2O, H

2O-NaCl and

H2O-NaF at 800 °C and 1 GPa: implications for REE transport during

high-grade metamorphism

163 PET25

26 P TROPPER, Peter Petrological investigations of contact metamorphic monticellite and clintonite-bearing skarns from the Cima di Miniera (South Tyrol, Italy)

79 PET26

27 P TROPPER, Peter Petrological investigations of Ti-phase relations in the metarodingites of Burgum, Pfitsch Valley (South Tyrol, Italy)

64 PET27

28 P TROPPER, Peter The metamorphic evolution and thermobarometry of amphibolites from the Pflersch-metadiorite complex (Pflersch valley, South Tyrol, Italy)

32 PET28

29 P VETLÉNYI, Enikô Study of silicate melt inclusions in olivine and spinel phenocrysts in alkaline basalt from Daljeon-Ri (Pohang, Central Korea)

170 PET29

GEOCHEMISTRY (GCH)

presenting author title of presentation page code

1 O BEQIRAJ, Arjan Geochemistry and petrogenesis of Bulqiza peridotites 31 1B3

2 O DEMÉNY, Attila Hydrogen isotope compositions of hydrous components in carbonado diamond

48 1B5

4 O GÖD, Richard On the geochemistry and mineralogy of phyllite-hosted tourmalinites – Eastern Alps

61 2B10

5 O HÖLLEN, Daniel Formation of amorphous silica and polymeric silicic acids by cylic freezing in various aqueous solutions

65 3B2

6 O KARAOGLAN, Fatih Geochronology and isotope geochemistry of the ophiolites and granitoids along the southeast Anatolian orogenic belt

73 1B7

7 O KISS, Gabriella Neotethyan advanced rifting stage peperitic basaltic volcanism in the Dinarides and Hellenides

77 1B2

8 O KLÉBESZ, Rita Comparison of the Hungarian ultrapotassic rocks based on mineral chemistry and textural characteristics

80 3B5

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11

GEOCHEMISTRY (GCH) – contimued

presenting author title of presentation page code

9 O SÁGI, Tamás Putikov Vŕšok, the youngest basaltic volcano of the Carpathian-Pannonian Region

139 3B4

10 O VETÔ, István Association of H2S – ankerite – late pyrite suggests active

thermochemical sulphate reduction below 5 km in the Pannonian Basin, SE Hungary

171 3B1

1 P AIGLSPERGER, Thomas Titanite-bearing pegmatites from Arkaroola, South Australia 20 GCH

2 P ATRSAEI, Parastoo A genetic model for banded magnetite-barite deposits in Mooteh area, West-Central Iran

25 GCH2

3 P BONDAR, Roman Peculiarities of the gaseous phase of the mineral forming fluids of metamorphic rocks of the Berlebash suite of Marmarosh massif, Ukrainian Carpathians, according to fluid inclusion studies

34 GCH3

4 P BONDAR, Roman Hydrocarbon volatile components of fluid inclusions in hydrothermal minerals of the Trostyanets volcanogenic complex (Ukrainian Carpathians)

35 GCH4

5 P DOLNIČEK, Zdeněk Post-magmatic hydrothermal alteration of igneous rocks of teschenite association (Silesian Unit, Outer Western Carpathians): Evidence from associated fracture and amygdule mineralization

51 GCH5

6 P DOPPLER, Gerald Trace elements in gem corundum (ruby) 52 GCH6

7 P KÁRMÁN, Krisztina Stable isotopes and hydrogeochemical parameters in a riverbank filtration system (Szentendre Island, Hungary)

74 GCH7

8 P KRIBITZ, Gerald A. Fluids in sulfide-bearing skarns, Carles (NW Spain) 91 GCH8

9 P MATVIYISHYN, Zoryana Typomorphic peculiarities of fluid inclusions of gold-bearing parageneses of ore stockwork bodies of Beregovo ore field (Transcarpathia)

113 GCH9

10 P MIRWALD, Peter W. Comparison of the thermal expansion behaviour of ice and the related high pressure phase topology of H

2O

104 GCH10

11 P NIEDERMAYR, Andrea Magnesium and strontium incorporation and calcium isotopic fractionation during calcium carbonate formation at low temperatures(5 to 40 °C)

116 GCH11

12 P PAUSCH, Martin Liquid membrane permeation with support layers in heavy metal recycling

123 GCH12

13 P POBEREZHSKYY,Andriy

A contribution to the regularities of alterations of chemical sedimentation in the Badenian evaporite basin of Precarpathia

129 GCH13

14 P STUPKA, Oksana Ophiolites of the Ukrainian Carpathians – New insights into the problem 151 GCH14

15 P SZABÓ, Zsuzsanna Comparison of two radon and thoron mapping methods 154 GCH15

16 P VÖLGYESI, Péter Radiometric measurements on fly ash and slag bearing buildingmaterials – A Hungarian case study

174 GCH16

17 P ZAHARIA, Luminiţa Geochemical characteristics of Ielova gneisses(South Carpathians, Romania)

179 GCH17

18 P ZEIRINGER, Isabella Activity and nature of skarn-building fluids in the metamorphic complex of the Lys-Caillaouas Massif (Central Pyrenees)

180 GCH18

MINERAL DEPOSITS (DEP)

presenting author title of presentation page code

1 O AIGLSPERGER, Thomas First discovery of platinum group minerals in Costa Rica 178 2A2

2 O AZIM ZADEH,Amir Morteza

The Hohentauern/Sunk deposit – A key for unravelling sparry magnesite formation in the Graywacke Zone/Eastern Alps, Austria

26 2A4

3 O FÖLDESSY, János MVT base metal mineralization in Rudabánya (NE Hungary) - Changes of genetic interpretation

58 2A3

4 O GÁL, Benedek Magmatic vs. hydrothermal processes in the South Filson Creek mineralization, South Kawishiwi Intrusion, Duluth Complex

59 2A5

5 O MOGESSIE, Aberra Mineral chemistry of platinum alloys from the historical placer deposits of Yubdo Complex, Ethiopia

108 2A1

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12

MINERAL DEPOSITS (DEP) – contimued

presenting author title of presentation page code

1 P AZIM ZADEH, Amir Morteza

Investigation of platinum group minerals (PGM) in chromite of Iran (Khoy Ophiolite) using electron microprobe

27 DEP01

2 P CORA, Ildikó Nano-sized mineralogy of a Toarcian manganese deposit (Úrkút, Hungary) and the importance of Mn3+ in its genesis

A6 DEP02

3 P DIMITROVA, Dimitrina A. Minor and trace elements in some ore minerals from the Chiprovtsi ore district, Northwestern Bulgaria

50 DEP03

4 P KISS, Péter Hydrothermal alteration, fluid inclusion characteristics and K/Ar ages for the intrusive volcanic-hydrothermal system of the Zlatá Baňa Volcanic Edifice (Slanské vrchy Mts., Eastern Slovakia)

78 DEP04

5 P MAJZLAN, Juraj Ore mineralization at the Rabenstein occurrence near Banská Hodruša, Slovakia

98 DEP05

6 P MOLNÁR, Ferenc Characterization of hydrothermal alteration assemblages of ‘low-sulphide’ Cu-Ni-PGE mineralization (Wisner area, Sudbury structure, Canada)

165 DEP06

7 P ONUZI, Kujtim Industrial minerals and rocks of Albania 119 DEP07

8 P SZABÓ, Csilla Mineralogy and origin of the Piskanja borate deposit (Jarandol Basin, Serbia)

153 DEP08

9 P TAGHIPOUR, Nader Fluid inclusion microthermometry at the Miduk Porphyry Copper Deposit, Kerman Province, Iran

157 DEP09

10 P TROPPER, Peter The intrusion related Cu-Fe-Zn-Pb-Ag deposits of the Pfunderer Berg (South Tyrol, Italy): Fahlore composition and T-fS

2 conditions of

formation

92 DEP10

11 P TROPPER, Peter Mineral chemistry and breakdown reaction of fahlore from Schwaz-Brixlegg (Tyrol, Austria)

93 DEP11

12 P VASSILEVA, Rossitsa D. Pre-ore stage in the Madan Pb-Zn deposits, South Bulgaria 168 DEP12

13 P VASSILEVA, Rossitsa D. Madan Pb-Zn sulphide deposits as part of the Alpine-Balkan-Carpathian-Dinaride Province

169 DEP13

APPLIED, ENVIRONMENTAL and CLAY MINERALOGY (AEC)

pt presenting author title of presentation page code

1. Applied mineralogy

1 O DIEKAMP, Anja The occurrence of magnesite and hydromagnesite in medieval dolomitic lime mortars

33 1A7

2 O MITTERMAYR, Florian Concrete damaging processes from sulphate attack 49 1A9

2. Environmental and clay mineralogy

3 O BOLANZ, Ralph Geohazards associated with brown coal mining in Central Slovakia 33 1A7

4 O FARKAS, Izabella M. Mineralogy and chemical composition of metal mining waste dump samples

57 3A6

5 O KAINDL, Reinhard Mineralogical investigations of airborne dust in Tyrol 72 1A5

6 O KLIMKO, Tomáš Secondary Sb and Fe mineral phases as products of sulphide oxidation of tailings material at antimony deposits Dúbrava and Poproč (Slovakia)

81 1A6

7 O ROSTÁSI, Ágnes Clay mineralogy of Carnian (Upper Triassic) pelagic successions from the Transdanubian Range (Hungary): Palaeoenvironmental consequences

137 1A8

8 O VICZIÁN, István Teaching environmental clay mineralogy – Outlines of a university course

172 3A7

1. Applied mineralogy

1 P APOSTOLAKI, Chryssa The use of natural hydraulic lime mortars in restoration; transformation processes of binder hydraulic components during rapid and slow air slaking

21 AEC01

2 P BEQIRAJ GOGA, EnkeleidaTextural features of zeolitic rocks from Munella, Northern Albania 30 AEC02

3 P PERFLER, Lukas Defects, complex layer structures and stress effects in synthetic diamond single crystals

41 AEC03

4 P POLGÁRI, Márta Morphological and mineralogical biosignatures from different paleoenvironments

46 AEC04

5 P REPOUSKOU, Eftychia Refractory bricks obtained from dunite rocks of Lesvos Island, Greece 67 AEC05

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APPLIED, ENVIRONMENTAL and CLAY MINERALOGY (AEC) – contimued

presenting author title of presentation page code

6 P STANIMIROVA, Tsveta Anion relationships of borate anions in hydrotalcite structure 97 AEC06

7 P SZABÓ, Bernadett The mineralogical investigation of hazardous wastes 109 AEC07

8 P WEISSENBACHER, Michael

Synthetic ruby and cubic zircon dioxide: Surface modifications due to cutting, grinding and polishing

125 AEC08

2. Environmental and clay mineralogy

9 P CIESIELCZUK, Justyna Mineral tranformations due to combustion metamorphism in a coal waste dump in Wojkowice, Upper Silesia, Poland

41 AEC09

10 P CSÁKBERÉNYI NAGY, Dorottya

Crystallization and phase transition of mackinawite (FeS) 46 AEC10

11 P HOVORIČ, Róbert Sulphide oxidation of mine tailings sediments from abandoned Sb de-posit Medzibrod (Nízke Tatry Mts., Slovakia)

67 AEC11

12 P MÁDAI, Ferenc ARD-screening of site rocks from the Rudabánya base metal mineraliza-tion (NE Hungary)

97 AEC12

13 P NAGY, Hedvig Éva Source study of an extremly high radon-anomaly area (S Hungary) 109 AEC13

14 P SIPOS, Péter Association of trace elements with Fe-rich nodules in an alluvial soil 146 AEC14

15 P SZABÓ, Katalin Zsuzsanna Relationship of radioactivity and geology in the Central Hungarian Region (Pest County)

152 AEC15

ARCHAEOMETRY / SCIENCE HISTORY (ARC)

presenting author title of presentation page code

1 O IONESCU, Corina Pre- and post-firing minerals in ancient ceramics 69 2A10

1 P KELEMEN, Éva A comparative archaeometric study on the building material of churches from the Árpád and Middle Ages of the Southern Great Hungarian Plain (Alföld)

75 ARC01

2 P KRISTÁLY, Ferenc New data for the Roman Ages settlement history of Miskolc: Archaeological and archaeometrical investigations

161 ARC02

3 P NAGY-KORODI, István Provenance studies of the building stones used for the Calvary Church (Cluj-Napoca, Romania)

110 ARC03

4 P PAPP, Gábor Authentic (type and other original) specimens of minerals first described from the Carpathian region in the collection of the Natural History Museum, Vienna – A survey

121 ARC04

5 P PAPP, Gábor Zepharovich’s studies at the Academy of Mining and Forestry, Banská Štiavnica / Schemnitz / Selmecbánya

122 ARC05

6 P POP, Dana Electron microprobe data on Roşia Montană (Apuseni Mountains) gold: Towards a database for identifying ancient artefacts

131 ARC06

7 P STANIMIROVA, Tsveta Petrographic characteristics of the ceramics from the early mediaeval settlement in the vicinity of the Kapitan Andreevo village, Svilengrad municipality, South Bulgaria

54 ARC07

8 P SZILÁGYI, Vera First results on the archaeometric investigation of the Buda white ware (12th–15th century, North Hungary)

A11 ARC08

9 P THAMÓ-BOZSÓ, Edit Optically stimulated luminescence dating of sedimentson archaeological sites

160 ARC09

10 P TROPPER, Peter Monitoring the high-T breakdown behaviour of chlorite and biotite ± quartz with high-T XRD and DTA/TG and its application to slags from prehistoric sacrificial burning sites

143 ARC10

11 P TROPPER, Peter Mineralogical and chemical investigations of slags from two prehistoric smelting sides at the Mitterberg area

173 ARC11

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MITT.ÖSTERR.MINER.GES. 155 (2009)

CONTOURS OF A NEW THEORY ON CRYSTAL DISSOLUTION

Luttge, A.1 & Arvidson, R.S.1

1Rice University, Department of Earth Science MS-126, 6100 S. Main St., Houston, Texas 77005 USA

e-mail: [email protected]

We discuss current progress in the theoretical and empirical treatment of crystal dissolution.Our approach abandons the limitations of closed-form equations and conventional “rate laws”and moves forward to a treatment of crystal reaction kinetics as a dynamic, many-bodyproblem that must be solved stochastically. At the centre of our model is a fundamentalunderstanding of the kinetics at kink sites that govern the overall processes of both crystaldissolution and growth (Fig. 1).This change in treatment brings with it important consequences: it permits a morefundamental insight into the molecular surface processes and their cumulative result,including variation of rate within mineral systems, the effect of non-stoichiometriccompositions, the relationship of ordering and temperature, and related phenomena. Theseinsights potentially lead to a comprehensive theory of crystal dissolution and a unifieddissolution-growth theory. However, they also require conceptual revisions in our approach toproblems involving crystal-fluid interaction. First, we must re-examine our application of theconcept of reactive surface area that has proven to be a largely unquantifiable parameter.Second, we must reconcile the lack of a single or “true” value for a so-called “rate constant”.Instead, we suggest that a range of possible rates exists for any given mineral, with a certainprobability for any given rate within this range. These insights have significant implicationsand consequences for our ability to predict long term behaviour in systems of environmentalimportance, such as nuclear waste, corrosion, and weathering of rocks and soils, with furtherimplications for water quality and climate development.

Figure 1. Schematic representation of fundamental processes of crystal dissolution.

Plenary lecture PL1 A1

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15

MITT.ÖSTERR.MINER.GES. 156 (2010)

CRYSTAL CHEMISTRY OF LIGHT ELEMENTS IN MAJOR ROCK-FORMINGMINERALS

Robert, J.-L.

IMPMC, 140 rue de Lourmel, 75015 Paris, France

e-mail: Jean-Louis [email protected]

Light elements (Z < 10) play a major role in rock-forming minerals. Their presence has oftenbeen ignored in the last decades, because they are hardly detectable in standard EMPA. Thedevelopment of new analytical facilities, like EMPA with multi-layer detectors, SIMS,nuclear and vibrational methods, combined with local charge balance considerations led to therecognition of light elements as important constituents of major rock-forming minerals. All ofthem, besides nitrogen, have a constant valence state under naturally occurring conditions.Light elements are not randomly distributed. Local associations of two to three of them arefrequent. For example, we find that the replacement of OH– groups by F– in layer, ring anddouble-chain silicates favours the incorporation of Li+ in the structure.The behaviour of Li+ is interesting since its coordination ranges from tetrahedral in lab-prepared compounds, like sulphate and tungstate, to highly distorted 12-fold coordination inclinoamphiboles. In clinoamphiboles, Li+ can occupy M1 and M3 sites, replacing a divalentcation, as well as the pseudo-cubic M4 site, and also the large [12]A sites. It is also common in[6] coordination in lepidolites, where it collapses the miscibility gap between trioctahedraland dioctahedral micas, and as an interlayer element in layer silicates, where it can occupy atleast two types of six-fold coordinated sites.Another relevant light element is F, which frequently replaces the hydroxyl group in OH-bearing minerals, silicates (micas, amphiboles, tourmalines etc.), and phosphates. It enhanceslocal ordering and is depolymerising under magmatic conditions. The commonly admitted Fe-F exclusion is violated in many minerals, e.g. fluorannite, and buergerite. F– can also bepresent as an interstitial anion, in high-Si micas having a partial dioctahedral character, whichfrequently led to the rejection of analyses as for “too high F content”.Boron can occur in [3] and [4] coordinations. B3+ can replace Al3+, as a major element infeldspars like reedmergnerite, the boron equivalent of albite. The three-fold coordination ofB3+ is usual in tourmalines generated under low P and T conditions, but [4]B3+ is also knownin high-P metamorphic tourmalines related to olenite. Beryllium would deserve a systematicanalysis, in major rock-forming crustal minerals, typically in pegmatites and derivedmetamorphic rocks. The [4]-coordination of this divalent cation generally generates strongshort-range ordering.Nitrogen as a major element has the most interesting properties as N5+, i.e. as ammoniumcation, yields few proper phases (e.g. tobelite). It can seriously modify the swelling propertiesof clays and their ability to trap pollutants in waste deposits.Finally, hydrogen, the most abundant element in the Universe, is obviously present in hydrousphases (as OH groups and/or water). It frequently compensates local charge defects innominally anhydrous minerals, from the Earth mantle to the surface.

A2 Plenary lecture PL2

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MITT.ÖSTERR.MINER.GES. 155 (2009)

MAGNESIUM PHOSPHATES: FROM MOLECULAR STRUCTURES TOSTRONGLY CONDENSED MINERALS

Armbruster, T.

Mineralogical Crystallography, Institute of Geological Sciences, University of Bern, Freistr. 3, CH-3012 Bern,Switzerland

e-mail: [email protected]

Magnesium-phosphate minerals are structurally very special because in contrast to calciumphosphates they comprise on one hand highly hydrated molecular structures, in which PO4

units are kept in position by hydrogen bonds originating from Mg(H2O)62+ octahedra, and on

the other hand they form densely packed orthophosphate structures. As examples for highlyhydrated minerals, structure and formation conditions of e.g., cattiite ((Mg(H2O)6)3 [PO4]2 � 4H2O, CATTI et al., 1981; BRITVIN et al., 2002) and struvite (Mg(H2O)6NH4[PO4],FERRARIS et al., 1986) are discussed. As examples of densly packed magnesium-phosphateminerals, special emphasis is placed on the modulated series of triplite–wagnerite groupminerals (ARMBRUSTER et al., 2008). The space group for wagnerite (Mg,Fe)2PO4(F,OH)was considered to be P21/c with a = 9, b = 12.6, c = 11.9 Å, � = 108° until REN et al. (2003)reported a new polytype (space group Ia, a = 9, b = 31.5, c = 11.9 Å, � = 108°) namedwagnerite-5b as it has a five-fold superstructure along b relative to triplite Mn2PO4F andzwieselite Fe2PO4F (space group I2/a, a = 9, b = 6.5, c = 12 Å, � = 106°). Single-crystal X-ray and chemical data were obtained on 38 wagnerite samples (ARMBRUSTER et al., 2008)formed under conditions ranging from near surface in sediments to high temperatures(granulite facies) and ultrahigh-pressures. We found five “pseudo”-commensurate modulatedstructures (polytypes) in decreasing abundance: 5b (21 examples), 2b (12), 7b (3) and 9b (2)and 3b (1). Five additionally studied triplite–zwieselite samples from pegmatites showed the1b type structure. The crystal structures of all 6 polytypes have been refined from single-crystal X-ray data and imaged by HRTEM. The main structural difference among the variouspolytypes is modulation of the (F,OH) arrangement giving rise to different space groups andperiodicity along b. F-dominant triplite–zwieselite (mean octahedral radius: > 0.79 Å) has the1b polytype. The 5b polytype prevails in F-dominant, Fe,Mn-rich wagnerite (mean octahedralradius: 0.74-0.79 Å) and in Mg-rich samples (octahedral radius = 0.72 Å) with near F end-member composition. The single 3b wagnerite plots among the 5b samples but close to thetriplite–zwieselite (1b) boundary in terms of XF and mean octahedral radius. Mg-richwagnerite (octahedral radius = 0.72–0.73 Å) is characterized by the 2b polytype, whatever theOH content. 7b and 9b polytypes are found for compositions stradling the boundary of the 5band 2b fields with XF between 0.84 and 0.98. These broad relationships suggest a major rolefor compositional control in determining modulation periodicity.

ARMBRUSTER, T., CHOPIN, C., GREW, E.S., BARONNET, A. (2008): Geochim. Cosmochim. Acta, 72, 12S, A32.BRITVIN, S.N., FERRARIS, G., IVALDI, A., BOGDANOVA, A., CHUKANOV, N.V. (2002): Neues Jahrb.Mineral. Monatsh., 160-168.CATTI, M., FRANCHINI-ANGELA, M., IVALDI, G. (1981): Z. Kristallogr., 155, 53-64.FERRARIS, G., FUESS, H., JOSWIG., G. (1986): Acta Crystallogr., B42, 253-258.REN, L., GREW, E.S., XIONG, M., MA, Z. (2006): Can. Mineral., 41, 393-411.

Plenary lecture PL3 A3

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MITT.ÖSTERR.MINER.GES. 156 (2010)

CATION ORDERING IN SILICATES AS SHOWN BY ELECTRONCRYSTALLOGRAPHY

Dódony, I.

Department of Mineralogy, Eötvös Loránd University, Pázmány Péter sétány 1/C, H-1117 Budapest, Hungary

e-mail: [email protected]

The structure of many minerals cannot be measured using conventional single crystaltechniques due to their polycrystalline and fine-grained character. That is why non-conventional methods of structure analysis must be applied to obtain structural informationfundamental to the understanding of these minerals. Electron crystallography is a powerfulmethod for solving structures of crystals with sub-micrometer sizes that are too small for X-ray crystallography.Compared to X-ray crystallography, the main advantage of electron crystallography is thatthere is no so-called “phase problem” in it. We can retrieve the phases from Fourier-transformhigh-resolution images. One of the main advantages of electron crystallography over X-raysis that the phases of crystallographic structure factors can be obtained directly from HRTEMimages when the crystal is thin enough to almost satisfy the kinematic approximation.Electron crystallography operates in both real and reciprocal space, phase informationobtained from high-resolution transmission electron microscopy images can be incorporateddirectly into the deconvolution process of the projected charge-density map of the measuredobject.Electron diffraction (ED) patterns can also be used alone for structure determination, wherethe structure factor phases are determined by direct methods.As an example, a study of ordered and disordered substitution in pyrope is presented. Oneapproach to the crystallography of solid solutions is to use high-resolution transmissionelectron microscopy together with electron crystallography, a combination that has thepotential of resolving individual atomic species and, more commonly, their projectedcolumns. Focus will be given to both theoretical and experimental considerations fordetermining substituted positions in HRTEM images and the reliability of suchdeterminations. We do this using pyrope garnet, chosen because it is an important rock-forming silicate with several possible crystallographic sites for substitutions. Usingsimulations with realistic constraints of composition and experimental conditions, wedetermine and demonstrate the abilities of electron crystallography for the characterization ofboth random (i.e., non-periodic) and ordered (periodic) substitutions in a complex silicate.As another example, modulations both in the tetrahedral and octahedral sheets in antigoritestructure were studied using the unique opportunities of electron crystallography. The resultsclearly show the lack of four- and eight-membered silicate rings in the tetrahedral sheets forthe antigorite structure model supposed by KUNZE (1958).

KUNZE, W.G. (1958) Die Gewellte Struktur der Antigorits. II. Zeitschrift für Kristallographie, 110, 282-320.

A4 Plenary lecture PL4

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MITT.ÖSTERR.MINER.GES. 155 (2009)

HYDROUS DEFECTS IN PYROXENES

Stalder, R.

Institut für Mineralogie und Petrographie, Universität Innsbruck, Innrain 52f, A-6020 Innsbruck, Austria

e-mail: [email protected]

Pyroxenes are amongst the most important rock-forming minerals in terrestrial planets and,next to olivine, the most abundant constituents of the Earth’s upper mantle. Due to the abilityof pyroxenes to incorporate significant trace amounts of hydrogen as point defects (i.e.,distinctively higher amounts than other upper mantle minerals) they may be regarded as majorhosts for hydrogen in the upper mantle. Since the incorporated hydrogen has majorconsequences for the physical properties and mantle processes such as melting, the exactknowledge of incorporation and dehydration behaviour is of general interest in geochemistry,petrology, mineral physics and geophysics.In order to quantify the water content of nominally anhydrous upper mantle minerals, twomain strategies have been followed: (1) direct analyses of samples derived from upper mantlerocks (mostly xenoliths from volcanic rocks from the Earth’s mantle), which show watercontents around 200 wt. ppm H2O for orthopyroxene and around 400 wt. ppm H2O forclinopyroxene (GRANT et al., 2007); (2) high-pressure – high-temperature experiments,investigating the effect of pressure, temperature, oxygen fugacity, silica activity and otherchemical aspects on water incorporation. Water contents in the mineral phases observed bythis strategy are generally much higher than observed in natural samples, and for pyroxenescontents up to several thousand wt. ppm H2O have been observed (MIERDEL et al., 2007).Several interpretations for the gap between analysis of natural material and experimentalresults have been put forward: (1) Partial hydrogen loss during ascent to the Earth’s surface(MACKWELL & KOHLSTEDT, 1990), (2) interaction of different hydrous defects incomplex composed systems (STALDER et al., 2005) and (3) reduced water fugacity innatural systems (STALDER et al., 2008). In spite of steadily growing evidence for point defects in pyroxenes, indications for planardefects have hitherto not been found. However, some orthopyroxenes (both natural andsynthetic ones, but all with high amounts of Al) show features similar to hydrous phases, suchas chlorite. One possible interpretation is the survival of chlorite-like domains inorthopyroxene far beyond the stability field of chlorite, similar to OH-bearing humite-typelamellae, which survive in some mantle rocks well beyond the stability field of humite asplanar defects in olivine (HERMANN et al., 2007).

GRANT, K., INGRIN, J., LORAND, J.P., DUMAS, P. (2007): Contrib. Mineral. Petrol., 154, 15-34.HERMANN, J., FITZ GERALD, J.D., MALASPINA, N., BERRY, A.J., SCAMBELLURI, M. (2007): Contrib.Mineral. Petrol., 153, 417-428.MACKWELL, S.J., KOHLSTEDT, D.L. (1990): J. Geophys. Res., 95, 5079-5088.MIERDEL, K., KEPPLER, H., SMYTH, J.R., LANGENHORST, F. (2007): Science, 315, 364-368.STALDER, R., KLEMME, S., LUDWIG, T., SKOGBY, H. (2005): Contrib. Mineral. Petrol., 150, 473-485.STALDER, R., KRONZ, A., SIMON, K. (2008): Contrib. Mineral. Petrol., 156, 653-659.

Plenary lecture PL5 A5

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A6 To be published in Mitt. Öster. Miner. Ges., 156 (2010)

MITT.ÖSTERR.MINER.GES. 156 (2010)

NANO-SIZED MINERALOGY OF A TOARCIAN MANGANESE DEPOSIT (ÚRKÚT, HUNGARY) AND THE IMPORTANCE OF Mn3+ IN ITS GENESIS

Cora, I.1 & Weiszburg, T.G.1

1 Department of Mineralogy, Eötvös Loránd University, 1117 Pázmány P. stny. 1/C, Budapest, Hungary

e-mail: [email protected] Úrkút (Hungary) hosts the largest Toarcian Mn ore deposit in Europe. It consists of both carbonate and oxide ore sequences. We studied a complete carbonate profile, consisting of a black shale sequence with two Mn-bearing horizons. This is the first time when this very fine-grained (µm- and nm-sized), lamellar sedimentary sequence was traced by systematic, real micrometer scale studies, including structural (micro X-ray diffraction), textural, and chemical (SEM+EDS, cathodoluminoscope) observations, as well as TEM+ATEM characterization of the nm sized phases. These data contribute substantially to the earlier genetic models. The lamellar ore structure is a result of parallel or exclusive existence of phases recording redox conditions (and their changes). Mn occurs both in carbonate (Ca-rich rhodochrosite) and (recently subordinate) oxidic phases in the carbonate ore. Ore-forming carbonate minerals display a complex texture. Six different types of Mn-Ca carbonates were identified. The oxidic Mn phase of the carbonate sequence is manganite. In contrast to the assumptions of the previous genetic models no Mn4+-oxide phase was found. Fe occurs both in reduced and oxidized form (euhedral and, in limited layers, framboidal pyrite; goethite and sheet silicates). Manganite can be regarded as the primary ore accumulation form of Mn. As Mn3+ is not expected to be formed by bacterial activity, manganite may be a chemical precipitate formed during local oscillation of suboxic/oxic conditions near the seabottom in the general Toarcian anoxic/suboxic environment conveying continuously dissolved Mn2+ into the local system. In restored local suboxic conditions microorganisms could utilize first Mn3+, then Fe3+ when oxidizing organic material. With increasing concentration of Mn2+

aq and HCO3aq(org), fine grained Ca-rich rhodochrosite precipitated, and allotigenic calcite, such as Radiolarian pseudomorphs, was also metasomatised by Mn2+. This two-way Ca-rhodochrosite formation model explains the typical intermediate 13C values (~15‰) and the poor correlation between Mn and 13C values published earlier (Polgári et al., 1991). Zeolite present in the sequence is detrital and cannot be regarded as a direct marker for any potential volcanic activity (source of Mn). POLGÁRI, M., OKITA, P.M., HEIN, J.R. (1991): J. Sediment. Petrol., 361/3, 384-393.

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MITT.ÖSTERR.MINER.GES. 156 (2010)

NEW MINERALOGICAL DATA FROM THE ENVIRONS OF MÁD, TOKAJ MTS., HUNGARY

Menyhárt, A., Dódony, I. & Pekker, P.

Department of Mineralogy, Eötvös Loránd University, Pázmány Péter sétány 1/C, Budapest, H-1117 Hungary

e-mail: [email protected] Several mines are known in the hydrothermally altered rhyolite tuff in the environs of Mád, Tokaj Mts., NE Hungary. This study presents new data on mordenite and clinoptilolite, rectorite, iron oxide, halloysite, smectite and SiO2 phases from these mines. X-ray powder diffraction (XRPD), scanning (SEM) and transmission electron microscope (TEM) techniques were used to identify minerals and gain more details on their occurrence. The X-ray powder diffraction study of a sample from the Bomboly area indicates rectorite (as was known earlier), however, TEM images show only separate illite and smectite crystals without any evident structural connection among them. The zeolite minerals were identified on the basis of sets of their d(hkl) values and symmetries measured on selected-area diffraction patters. Their compositions were quantified simultaneously using energy dispersive X-ray (EDX) spectra acquired on the corresponding areas. The hydrothermally altered rhyolite tuff at Harcsa-tet Hill contains a Na-free, Ca-containing zeolite, which corresponds to mordenite according to XRPD results, whereas at Suba-oldal area clinoptilolite occurs with additional Mg and K as exchangeable cations. At Suba-oldal smectite and a SiO2 phase can also be found. Using TEM the thickness of the individual smectite flakes was determined and the SiO2 phase was identified as cristobalite. Király Hill was identified as a new locality of halloysite. An unusual iron oxide/hydroxide phase that has earlier been considered as hematite/ hydrohematite was recognised at Király Hill Although its XRPD diagram shows reflections interpretable as hematite, according to TEM data neither its structure nor its chemical composition comply with that of hematite.

To be published in Mitt. Öster. Miner. Ges., 156 (2010) A7

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MITT.ÖSTERR.MINER.GES. 156 (2010)

IRRADIATION DAMAGE IN MONAZITE: A RAMAN STUDY OF Au-IRRADIATED FIB FOILS

Nasdala, L.1, Grötzschel, R.2, Probst, S.2, Ruschel, K.1 & Hanchar, J.M.3

1Institut für Mineralogie und Kristallographie, Universität Wien, Althanstraße 14, A-1090 Wien, Austria

2Forschungszentrum Dresden-Rossendorf e.V., P.O. Box 510119, D−01314 Dresden, Germany 3Department of Earth Sciences, Memorial University of Newfoundland, St. John’s, NL A1B 3X5, Canada

e-mail: [email protected] In recent years, spectroscopy is increasingly being used to study mineralogical samples on a micrometre scale. Failure to consider critically the sample volumes analysed, however, may result in serious misinterpretations of results (for instance, see discussion by NASDALA, 2009). In a recent contribution, PICOT et al. (2008) described monazite samples that were irradiated with 1−7 MeV Au ions. They found in the TEM that near-surface volumes areas were fully amorphised, whereas Raman spectra still showed narrow, “crystalline” PO4 vibrational bands. PICOT et al. (2008) concluded that phosphate groups must be remarkably irradiation-resistant units that remain undamaged in spite of the bulk amorphisation. We believe this conclusion is incorrect; simply caused by the failure to consider the real depth resolution of the Raman analysis system used. Monte Carlo simulations predict that the irradiation of monazite done by PICOT et al. (2008) resulted in a damaged layer of not much more than 1 µm thickness (Fig. 1a). Given the real depth resolution of modern confocal Raman systems (≥2 µm), it appears more than likely that PICOT et al. (2008) also analysed the underlying, undamaged host monazite as well as the irradiated layer. We report first results of our experiments, which were done analogous to those of PICOT et al. To rule out the above uncertainty, however, we used ∼1 µm thick monazite foils (Fig. 1b) that were prepared using a focused ion beam system and placed atop a “Raman-inert” sample holder.

Figure 1. (a) Defect distribution in monazite irradiated with 1 MeV (dotted curve), 3.5 MeV (dashed curve), and 7 MeV Au ions (dot-dash curve) as predicted by Monte Carlo simulations. Solid line = total defects. (b) FIB-cut monazite lamella (size ca. 20×12×1 µm3), attached to a steel sample holder by local Pt deposition at its angles. NASDALA, L. (2009): Am. Mineral., 94, 853-855. PICOT, V., DESCHANELS, X., PEUGET, S., GLORIEUX, B., SEYDOUX-GUILLAUME, A.M., WIRTH, R. (2008): J. Nucl. Mater., 381, 290-296.

A8 To be published in Mitt. Öster. Miner. Ges., 156 (2010)

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MITT.ÖSTERR.MINER.GES. 156 (2010)

TEM STUDY OF AMORPHOUS IRON OXIDE PRECIPITATES FROM THE MÁTRASZENTIMRE Pb-Zn ORE MINE, MÁTRA MTS., HUNGARY

Pekker, P., Dódony, I. & Weiszburg, T. G.

Department of Mineralogy, Eötvös Loránd University, Pázmány Péter sétány 1/C, Budapest, H-1117 Hungary

e-mail: [email protected] Amorphous and nanocrystalline iron oxides are very common in acid mine environment, originating from the decomposition of iron sulfide (pyrite). Our samples originate from the precipitate of the acid mine drainage of a Pb-Zn ore mine near the village Mátraszentimre (Mátra Mts., North Hungary). The fresh bulk sample looks like a red jelly consisting of solid iron oxide/hydroxide and electrolite of water-soluble ions (pH 6.7, Ca, Al, Zn, As, [SO4], [PO4]). The iron oxide component was separated by repeated leaching in distilled water followed by centrifugal extraction. Analytical transmission electron microscope techniques (TEM, HRTEM, TEM tomography, SAED, EDS) were applied to investigate morphology, structure and chemical composition of the iron oxide/hydroxide phases. Two types of iron oxide/hydroxide were recognised, which differ in both morphology and chemical composition: a rounded (Fig. 1) and a needle-like one (Fig. 2). To characterise morphology we used TEM tomography. The rounded iron oxides are 100.200 nm plates, in their chemical composition the Fe (+Si,Al) : O atomic ratio is 1 : 3 and the As content is 2.8 wt%. The needle-like iron oxides are 50 nm long needles aggregated into 100.200 nm spheres. Their Fe (+Si,Al) : O atomic ratio is 1 : 2 and the As content is 2.5 wt%. We calculated pair-distribution functions (PDF) from electron diffraction patterns (SAED) to determine specific atomic distances for both iron oxide types.

Figure 1. Rounded iron oxide plates.

Figure 2. Aggregates of needle-like iron oxides.

To be published in Mitt. Öster. Miner. Ges., 156 (2010) A9

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MITT.ÖSTERR.MINER.GES. 156 (2010)

MINERALOGICAL EXAMINATION OF HAZARDOUS WASTES

Szabó, B. & Weiszburg, T. G.

Department of Mineralogy, Eötvös Loránd University, Pázmány Péter sétány 1/C, Budapest, H-1117 Hungary

e-mail: [email protected]

In Hungary, like in the whole European Union, there is an increasing demand for waste recycling in contrast to waste deposition. Parallel to that tendency, the application of natural resources (e.g. clay as pure geological medium) during the construction, running and rehabilitation of solid waste repositories is getting more and more limited. The present study aims to combine the above outlined two environment-sensitive industrial approaches by substituting the clean geological medium by properly treated solid hazardous wastes in the course of the rehabilitation of waste piles. In a first stage five different solid waste types, all of them classified as hazardous, were examined for their mineralogical and geological characteristics, including chemical and phase composition. In a second, currently still running stage these wastes have been treated in different ways in order to stabilize them adequately. X-ray powder diffraction, SEM+EDX and partial wet chemical analysis were performed on 1) fly ash of a communal incinerator; 2) sewage sludge residue from the cleaning of smelter gas; 3) a mud-consistency residue of gas cleaning in a former gas factory (“gas mud”); 4) cutting and milling waste of a metal processing company and 5) CaF2-containing mud waste from lighting industry. Four different treatments were applied to the fly ash (waste type 1) of the communal incinerator. The above mentioned analytical techniques were also used to characterise the treated samples of the fly ash. The treatment with a Na2SO4-dominant leachate, itself also a waste material, seemed to be the only one properly fixing the toxic components of the fly ash. When a limited amount (around 10 vol%) of cement was added to the fly ash + Na2SO4-dominant leachate mixture, the dissolution of toxic elements was already above the threshold limit values given by the environmental standards. Our results show that the treated fly ash, besides its proper chemical behaviour, is also of the engineering advantage that it behaves like concrete. In its original, fresh form it is plastic, it can fill up the voids and fissures of the deposited mixed solid wastes of the repository, while in a few weeks it hardens and limits largely the water circulation within the repository. The reduced amount of circulating water decreases the environmental risk of the rehabilitated repository. The treated fly ash can also be used for covering the filled-up repository, thus it is a good candidate for being a substitute of a suitable clean geological medium. At the sewage sludge (waste type 2) the high zinc content is the barrier of its direct metallurgical use. We found that part of the zinc in the waste, present as micrometer-sized zinc sulphide grains embedded in calcite, is easy to remove, however the other part, built in the spinel structure, needs further development of the separation techniques. The “gas mud” (waste type 3) is chemically and mineralogically too complex for a similar usage in rehabilitation, but further chemical processing tests may lead to techniques where a larger amount of the non-toxic metal content can be extracted and reused in metallurgy, while the total volume of the hazardous solid waste to be deposited will be largely reduced. Further studies for the application of the waste types in waste repository use are in progress.

A10 To be published in Mitt. Öster. Miner. Ges., 156 (2010)

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MITT.ÖSTERR.MINER.GES. 156 (2010)

FIRST RESULTS OF THE ARCHAEOMETRIC INVESTIGATION OF THE BUDA WHITE WARE (12TH–15TH CENTURY, NORTH HUNGARY)

Szilágyi, V.1, Gál-Mlakár, V.2, Rácz, T.Á.3, Sajó, I.4 & Simonyi, E.5

1Institute of Isotopes, HAS, Budapest, Konkoly-Thege M. út 29-33, H-1121 Hungary

2Herman Ottó Museum, Miskolc, Görgey Artúr u. 28, H-3529 Hungary 3Ferenczy Museum, Directorate of Pest County Museums, Szentendre, F tér 6, H-2000 Hungary

4Chemical Research Center, HAS, Budapest, Pusztaszeri út 59-67, H-1025 Hungary 5Hungarian National Museum, Budapest, Múzeum körút 14-16, H-1088 Hungary

e-mail: [email protected]

There was a special white ware in Buda, the capital of the Hungarian Kingdom in the Middle Ages. It basically consisted of table ware (bottles) with thin walls, sometimes red painting but more often engraved decoration. According to HOLL (1963), the ‘Buda white ware’ appeared during the 13th century and spread over the middle and northern part of the kingdom. It was his suggestion that the manufacturing happened somewhere in the near-Buda rural pottery workshops (domestic industry). However, some contradictory evidence emerged during the later researches. This special pottery can also be found in pre-13th century contexts. In the archaeological assemblages of the northern parts of the Hungarian Kingdom (present Slovakia) it is interpreted as an imported product and there is no obvious raw material in the region of Buda for this kind of pottery. The aim of our research was to give preliminary archaeometric data about this special white ware by microscopic petrographic observations and basic mineralogical investigations (XRPD). Although in the first stage of the research it was possible to investigate only a limited number of ceramic finds, differences in raw material usage could be proved. The analyzed fragments came from archaeological sites of the 12th–14th centuries in different distances from Buda. According to the archaeological observations of Gál-Mlakár (2008), three types of the ‘Buda white ware’, namely ‘yellowish white’, ‘white’ and ‘greyish white’ can be macroscopically distinguished in the excavated assemblages from the eastern part of the kingdom. However, these types cannot be observed distinctly in the archaeological sites to the west. Investigating ceramic artefacts from some East Hungarian sites (Komlóska, Füzér, Sárospatak) we were able to distinguish differences in the mineralogical composition of the three archaeological types of ‘Buda white ware’. Although it was common in every type that very fine-grained, very plastic clay was used as the paste of pottery and it was tempered with sand derived from low-grade metamorphic and granitoid rocks, three different clay types could be identified as the paste. The ‘yellowish white’ type of ‘Buda ware’ which is pleochroic under the microscope has illite-smectite mixed layer silicate composition. The paste of the ‘white’ type of ‘Buda ware’ is characterised by iron-free illitic-smectitic clay, while that of the ‘greyish white’ type is illitic in composition. Results are less clear-cut for ceramic fragments from sites in the western part of the distribution area (Fels zsolca, Üll , Maglód, Vecsés, Gyál). They can partly be classified into these three material types but in some cases they look like objects or lower quality imitations made from almost the same raw clays. GÁL-MLAKÁR, V. (2008): Komlóska-Pusztavár. Miskolc. HOLL, I. (1963): Budapest Régiségei, 20, 335-382.

To be published in Mitt. Öster. Miner. Ges., 156 (2010) A11

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ABERRA, Mogassie 115ABU-ALAM, Tamer Sabry 17, 18,

19AFTABI, Alijan 157AIGLSPERGER, Thomas 20, 178ALIREZAEI, Saeed 25AMTHAUER, Georg 62APOSTOLAKI, Chryssa 21ARMBRUSTER, Thomas 22 (A3)ARROYABE, Erik 23ARVIDSON, Rolf 96 (A1)ASAN, Kursad 95ATANASSOVA, Radostina G. 24,

169ATRSAEI, Parastoo 25AZIM ZADEH, Amir Morteza 26,

27BAČÍK, Peter 28BAČO, Pavel 78BADENSZKI, Eszter 115BAJNÓCZI, Bernadett 48BAKKER, Ronald J. 20, 91, 180BARGOSSI, Giuseppe 144BARTUCZ, Dorottya 170BATKI, Anikó 29BAUERNHOFER, Andreas 63BELETE, K. Hailu 108BENEA, Marcel 68, 131BEQIRAJ, Arjan 31BEQIRAJ GOGA, Enkeleida 30BERAN, Anton 158BERNABE, Egon 32BERTOLDI, Christian 143BIGI, Simona 87BÖHM, Florian 116BOLANZ, Ralph 33BONDAR, Roman 34, 35BÓNOVÁ, Katarina 37BOROS, Ákos 152BOTTA, Claudio 36, 72BÖTTCHER, Michael 106BREITNER, Dániel 109, 174BROSKA, Igor 37, 127BRUAND, Emilie 38BUDA, György 39BURCHARD, Michael 102CAMPOS, Lolita 178

CARAN, Semsettin 43, 44CHOVAN, Martin 81CHUDÍK, Peter 40CIESIELCZUK, Justyna 41ÇINA, ALEKSANDER 42CÎNTĂ PÎNZARU, Simona 68COBAN, Hakan 43, 44ČOPJAKOVÁ, Renata 45CORA, Ildikó A6CSÁKBERÉNYI-NAGY,

Dorottya 46, 117DALLAI, Luigi 43, 44DEÁK, József 74DÉGI, Júlia 47DEMÉNY, Attila 48DIEKAMP, Anja 49DIETZEL, Martin 65, 106, 116DIMITROVA, Dimitrina A. 50DING, Kuishou 177DÓDONY, István 117, 120, A4, A7,

A9DOLNÍČEK, Zdeněk 51DOPPLER, Gerald 52DRÁBEK, Milan 53DROZD, Vadym 48DYANKOVA, Galina 54EBNER, Fritz 26EISENHAUER, Anton 116ERTL, Andreas 55ETEMAD-SAEED, Najmeh 56FARKAS, Izabella M. 57FEKETE, Szandra 128FINGER, Fritz 150FLOWER, Martin 44FÖLDESSY, János 58, 97FÖLDVÁRI, Mária 88, 171FÓRIZS, István 74FORRAY, Ferenc 131FRITZ, Harald 63FRITZ, Marlene 123GÁL, Ágnes 110GÁL, Benedek 59GÁL-MLAKÁR, Viktor A11GARAI, József 48GARUTI, Giorgio 108, 178GATTA, G. Diego 102GHORBANI, Ghasem 60

GIESTER, Gerald 133, 177GLASMACHER, Ullrich A. 102GÖD, Richard 61GRECHANOVSKAYA, Elena

E. 99, 100GRODZICKI, Michael 62GRÖTZSCHEL, Rainer A8GSPAN, Christian 125GÜNES, Zekeriyas 82HÄGER, Tobias 167HANCHAR, John M. 112, A8HAR, Nicolae 68HARANGI, Szabolcs 71, 76, 80, 139HARLOV, Daniel 163HAUZENBERGER, Christoph A. 52,

63, 86, 90, 111, 156HEGNER, Ernst 48HEISS, Gerhard 61HEJNY, Clivia 140HIDAS, Károly 85, 155HIDEN, Susanne 64, 72HOANG, Nguyen 44HOECK, Volker 69, 84HOINKES, Georg 90, 134HÖLLEN, Daniel 65HOLZMANN, Jan 66, 72HOMONNAY, Zoltán 88HORVÁTH, Ákos 109, 154HOSSEINI-BARZI, Mahboobeh 56HOVORIČ, Róbert 67HYBLER, Jiří 53IANCU, Ovidiu Gabriel 68ILIEVA, Albena 54IONESCU, Corina 68, 69, 84, 110,

131JÁGER, Viktor 70JANKOVICS, Éva 71JIANG, Shao-Yong 26JONES, Peter C. 165JURKOVIČ, Ľubomir 33, 81KADIOĞLU, Yusuf Kağan 95KAHLENBERG, Volker 23, 36,

125, 175KAINDL, Reinhard 23, 72, 125, 175KÁKAY SZABÓ, Orsolya 88KÁLDOS, Réka 170KANSUN, Gürsel 95

Index of authors

Authors of the abstracts published in the Mitteilungen der Österreichischen Mineralogischen Gesellschaft, Vol. 155, 2009 and in this programme booklet. Numbers refer to the page of the Mitteilungen, containing the relevant abstract. Numbers starting with A refer to the page numbers of the abstract pages of this programme booklet.

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KARAKAŞ, Mustafa 95KARAOGLAN, Fatih 73KÁRMÁN, Krisztina 74KELEMEN, Éva 75KERESTEDJIAN, Thomas 169KISAKÜREK, Basak 116KISS, Balázs 76KISS, Gabriella 77, 153KISS, Péter 78KLAMMER, Dietmar 106KLAUSER, Frederik 125, 175KLAUSNER, Sonja 79KLÉBESZ, Rita 80KLIMKO, Tomáš 67, 81KLOETZLI, Urs see KLÖTZLIKLÖTZLI, Urs 63, 73, 82, 141KOÇAK, Kerim 95KÖHLER, Stephan J. 65, 106, 116KOLITSCH, Uwe 83, 121, 176KOLLER, Friedrich 39, 73, 84, 115KONC, Zoltán 85, 170KONRAD, Lukas 86KONZETT, Jürgen 49, 86, 90KÓNYA, Péter 87, 88KOVÁCS-PÁLFFY P. 88KOZLIK, Michael 72, 89KRAMAR, Sabina 112KRENN, Kurt 90, 141KRIBITZ, Gerald A. 91KRISMER, Matthias 92, 93KRISTÁLY, Ferenc 94, 161KROPÁČ, Kamil 51KUBIŠ, Michal 127KUBUKI, Shiro 88KUPI, László 58KURT, Hüseyin 95LALINSKÁ, Bronislava 67, 81LAZARENKO, Elena (Olena) E. 99,

100LEIS, Albrecht 106LEKA, Xhovalin 119LENGAUER, Christian L 138LEWIS, John 178LIBOWITZKY, Eugen 138, 167LINNER, Manfred 149LOERTING, Thomas 104LOSOS, Zdeněk 158LUTTGE, Andreas 96 (A1)MÁDAI, Ferenc 97MAIR, Volkmar 64, 66, 79, 136 MAJZLAN, Juraj 33, 98MALI, Heinrich 108MANNING, Craig 163, 164MARCHEV, Peter 169MARKOPOULOS, Theodoros 21

MAROCCHI, Marta 144MASCLE, Georges H. 159MASI, Umberto 31MATVIYISHYN, Zoryana 113MAY, Zoltán 146MAYR, Andreas 72MEHOFER, Mathias 167MELNIKOV, Volodymir S. 99, 100MENYHÁRT, Adrienn A7MESIARKINOVÁ, Martina 101MILETICH, Ronald see MILETICH-

PAWLICZEKMILETICH-PAWLICZEK,

Ronald 102, 140MIRON, Dan G. 103MIRWALD, Peter W. 49, 104, 105MITTERMAYR, Florian 106MLADENOVA, Vassilka, G. 50MOAYYED, Mohssen 27MOAZZEN, Mohssen 107MOGESSIE, Aberra 108, 124, 141,

165MOISSL, Angela-Patricia 102MOLNÁR, Ferenc 59, 70, 77, 78,

124, 153, 165MUHONGO, Sospeter 63MÜLLER, Alexandra 130MULLER, Fabrice 30MUSKE, József 88NAGY, Géza 39, 48NAGY, Hedvig Éva 109NAGY-KORODI, István 110NANTASIN, Prayath 111NASDALA, Lutz 112, 138, 167, A8NAUMKO, Ihor 34, 35, 113NECHEPURENKO, Oleksandr O. 34NÉDLI, Zsuzsanna 114NÉMETH, Bianca 115NÉMETH, Norbert 58NÉMETH, Tibor 146NEUMANN, Reinhard 102NIEDERMAYR, Andrea 116NOLL, Hannes 123NTAFLOS, Theodoros 71, 76, 80,

139NYIRÔ-KÓSA, Ilona 117ONDREJKA, Martin 37, 118, 166ONUZI, Kujtim 84, 119ORBÁN, Richárd 120OZDÍN, Daniel 101PALINKAŠ, Ladislav A. 77PÁL-MOLNÁR, Elemér 29, 39, 130PAPP, Gábor 121, 122PARLAK, Osman 73PASZKOWSKI, Mariusz 41

PAUSCH, Martin 123PÉCSKAY, Zoltán 78PEKKER, Péter A7, A9PÉNTEK, Attila 124PERDIKATSIS, Vassilis 21PERESSINI, Gabriella 82PERFLER, Lukas 72, 125PERTLIK, Franz 126PETAUTSCHNIK, Christian 112PETERSON, Dean M. 59PETRÍK, Igor 37, 127PINTÉR, Zsanett 128PIPPINGER, Thomas 140POBEREZHSKYY, Andriy 129POLACH, Martin 51POLGÁRI, Márta 130POP, Dana 68, 131PÓSFAI, Mihály 46, 117,

programme back coverPOWELL, Roger 38PRECHTEL, Felix H. N. 132PREUSCHL, Frederik 112, 133PRINCIVALLE, Francesco 114PRISTACZ, Helmut 83, 112, 133PRISTAVOVA, Stefka 54PROBST, Sylvio A8PROENZA, Joaquin 178PROYER, Alexander 38, 134PRSEK, Jaroslav 118PUHR, Barbara 134QUICK, James E. 82RÁCZ, Tibor Ákos A11RAUCSIK, Béla 137RECHEIS, Arno 52REČNIK, Aleksander 46, 117REDHAMMER, Günther 62, 102REISSNER, Michael 62REPOLUST, Thomas 90REPOUSKOU, Eftychia 135RÉVAY, Zsolt 88RHEDE, Dieter 138RIEDER, Milan 53ROBERT, Jean-Louis A2ROFNER, Verena 136ROSTÁSI, Ágnes 137RUSCHEL, Katja 112, 138, A8SÁGI, Tamás 71, 139SAGL, Raffaela 72, 140SAJGÓ, Csanád 171SAJÓ, István A11SAKHNO, Bogdan 34, 35SAMART, P. 111SCHEIPL, Gregor 141SCHLAMADINGER, Michael 52SCHMITT, Martin 102

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SCHNEIDER, Philipp 72, 142, 143SCHOTTENBERGER, Herwig 105SCHUSTER, Ralf 134, 149SEIWALD, Manuela 144SHAFAII MOGHADAM, Hadi 145SHARYGIN, Victor 85, 170SIEBENHOFER, Matthäus 123SIMONYI, Erika A11SINIGOI, Silvano 82SIPOS, Péter 146ŠKODA, Radek 45SOMMER, Holger 86STALDER, Roland 132, 147 (A5)STANIMIROVA, Tsveta 54, 148STEIDL, Magdalena 72, 149STEINER, Walter 62STÖBICH, Eva 72, 150STÖLLNER, Thomas 173STUEWE, Kurt see STÜWESTUPKA, Oksana 151STÜWE, Kurt 17, 18, 19, 38SUTTHIRAT, Chakkaphan 52SZABÓ, Ábel 155SZABÓ, Bernadett A10SZABÓ, Csaba 74, 85, 109, 114,

115, 128, 152, 154, 155, 170, 174SZABÓ, Csilla 153SZABÓ, Katalin Zsuzsanna 152SZABÓ, Zsuzsanna 154SZAKÁCS, Alexandru 110SZAKÁLL, Sándor 87, 94SZENDI, Attila 122SZILÁGYI, Vera A11

T. BIRÓ, Katalin 160TAFERNER, Harald 156TAGHIPOUR, Nader 157TALLA, Dominik 112, 133, 158TĂMAŞ, Calin 131TASHKO, Artan 159TCHOUANKOUE, Jean 128TELEPKO, Larysa 35TENCZER, Veronika 63TENE DJOUKAM, Joelle Flora 128TESSADRI, Richard 89THALHAMMER, Oskar 178THAMÓ-BOZSÓ, Edit 160, 171THÖNI, Martin 73THÖNY, Werner Friedrich 162TILLMANNS, Ekkehart 55, 176,

177TÖBBENS, Daniel M. 23, 36TÖRÖK, Kálmán 47, 115TÓTH, Attila 155TÓTH, Krisztián 161TOURAY, Jean C. 30TRAUTMANN, Christina 102TRIBUS, Martina 162TROPPER, Peter 32, 64, 66, 79, 89,

92, 93, 136, 142, 143, 144, 149, 150, 162, 163, 164, 173

TUBA, Györgyi 165UHER, Pavel 28, 40, 51, 118, 166ULLRICH, Angela 140UNGERANK, Daniel 66, 72URUBEK, Tomas 51UYSAL, Ibrahim 27

VÁCZI, Tamás 167VARGA-BARNA, Zsuzsa 171VASSILEVA, Rossitsa D. 168, 169VAVTAR, Franz 66, 92, 93, 173VETLÉNYI, Enikô 170VETÔ, István 171VICZIÁN, István 172VIERTLER, Hans-Peter 173VIERTLER, Johann 72VÖLGYESI, Péter 174VYNNYCHENKO, Tamara 35WALLBRECHER, Eckar 63WATHANAKUL, Pornsawat 111WATKINSON, David H. 124, 165WEIKUSAT, Christian 102WEISSENBACHER, Michael 72,

175WEISZBURG, Tamás G. 57, A6,

A9, A10WERTL, Waltraud 36, 143WIERZBICKA-WIECZOREK,

Maria 176WILDNER, Manfred 133WILLI, Thomas 102WIRTH, Richard 138, 167WYHLIDAL, Stefan 162YANG, Kiaong Hee 170YANG, Zhuming 177YILMAZ, Kamil 43, 44ZACCARINI, Federica 20, 27, 108,

178ZAHARIA, Luminiţa 179ZEIRINGER, Isabella 180

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Surroundings of the Eötvös University, Riverside Campus (Lágymányos)Venue of the MinPet2009 & 4thMSCC joint meeting

Eötvös Loránd University (Building C), 1117 Budapest, Pázmány Péter sétány 1/C

A la carte self-service restaurant, Infopark, Building D

A la carte self-service restaurant, Infopark, Building I

Technical University, self-service restaurant, Goldmann György tér 1 (on the first floor)

Chinese fast food restaurant (Karinthy Frigyes út 21)

Tram station “Petõfi híd, budai hídfõ” (Petõfi Bridge, Buda side), of trams no. 4 and 6

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Dept. of Mineralogy

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Monday, September 713:00—20:00 Registration, mounting of posters / Field trip 1 13:00—20:0019:30—21:30 Ice breaker party 19:30—21:30

Tuesday, September 8 8:00—8:50 Registration, mounting of posters 8:00—8:50 9:00 Opening 9:00 9:15

Plenary lecturesPL1: Luttge 9:15

9:45 PL2: Robert 9:4510:15 Coffee/posters 10:1511:00

Crystallography

1A1: Amthauer

Geochemistry-Petrology 1

1B1: Koller 11:0011:20 1A2: Miletich 1B2: Kiss G. 11:2011:40 1A3: Talla 1B3: Beqiraj 11:4012:00 1A4: Arroyabe 1B4: Prechtel 12:0012:20 Lunchbreak 12:20

14:00POSTER DISCUSSION 1

coffee/beer14:00

16:00

Applied,environmental,and claymineralogy

1A5: Kaindl

Geochemistry-Petrology 2

1B5: Demény 16:0016:20 1A6: Klimko 1B6: Coban 16:2016:40 1A7: Bolanz 1B7: Karaoglan 16:4017:00 1A8: Rostási 1B8: Jankovics 17:0017:20 1A9: Diekamp 1B9: Kiss B. 17:2017:40 1A10: Mittermayr 1B10: Moazzen 17:4018:00—18:45 Public lecture PU1: Pósfai 18:00—18:45

Wednesday, September 9 8:30

Mineral deposits

2A1: Mogessie

Geochemistry-Petrology 3

2B1: Bruand 8:30 8:50 2A2: Aiglsperger 2B2: Klötzli 8:50 9:10 2A3: Földessy 2B3: Dégi 9:10 9:30 2A4: Azim Zadeh 2B4: Németh 9:30 9:50 2A5: Gál 2B5: Tropper 9:5010:10 Coffee/posters 10:1010:40

Generalmineralogy, Archaeometry

2A6: Çina

Geochemistry-Petrology 4

2B6: Buda 10:4011:00 2A7: Kristály 2B7: Broska 11:0011:20 2A8: Bačík 2B8: Kurt 11:2011:40 2A9: Jáger 2B9: Petrík 11:4012:00 2A10: Ionescu 2B10: Göd 12:0013:00—19:00 Field trip 2 Dunabogdány 13:00—19:0020:00 Conference dinner 20:00

Thursday, September 10 9:00

Plenary lecturesPL3: Armbruster 9:00

9:30 PL4: Dódony 9:3010:00 Coffee/posters 10:0010:30

Generalmineralogy,Teaching

3A1: Nasdala

Geochemistry-Petrology 5

3B1: Vető 10:3010:50 3A2: Uher 3B2: Höllen 10:5011:10 3A3: Ondrejka 3B3: Puhr 11:1011:30 3A4: Ertl 3B4: Sági 11:3011:50 3A5: Chudik 3B5: Klébesz 11:5012:10 3A6: Farkas 3B6: Shafaii 12:1012:30 3A7: Viczián 12:3012:50 Lunchbreak 12:50

14:30POSTER DISCUSSION 2

coffee/beer14:30

17:00 Plenary lecture PL5: Stalder 17:0017:30—17:45 Closing 17:30—17:4518:00 IMA2010 CRT meeting 18:00

Friday, September 11Field trip 3

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PROGRAMME

MinPet2009 & 4thMSCCJoint Conferencean “Eötvös Workshops in Science” meeting

Budapest, Hungary, September 7—11, 2009http://www.minpet2009mscc.org

PUBLIC LECTURETuesday, September 8, 6 pm

Lecture room 0.823

MITT.ÖSTERR.MINER.GES. 156 (2010)

BIOMINERALS

Pósfai, M.

University of Pannonia, Veszprém, H-8200 Hungary

e-mail: [email protected]

Why are our bones strong and tough, why are our teeth hard? How do mussels and snails build their shells? Why can bacteria and birds navigate in magnetic fields? The lecture attempts to give answers to these questions: in all cases a biological function, such as support, protection or orientation, is served by composites of organic materials and inorganic crystals – biominerals – that form inside the living organism (MANN, 2001). The sizes, shapes, compositions, structures and arrangements of the mineral grains in the organism are all tightly controlled by various biological mechanisms that affect crystal nucleation and growth (Fig. 1). The highly constrained properties of biominerals distinguish them from their inorganically-formed counterparts. The study of biominerals uses research techniques and knowledge from several disciplines, including mineralogy, biology, physics, materials science and geology. In this lecture, we will employ a cross-disciplinary perspective to broadly review the functions, formation mechanisms and properties of biominerals.

Figure 1. Two pairs of chains of magnetite (Fe3O4) nanocrystals in the cell of a magnetotactic bacterium. The white lines represent a map of the magnetic induction, as obtained from electron holography in a transmission electron microscope, while the colours show the direction of the magnetic induction according to the colour wheel shown in the lower left. The highly constrained sizes, shapes and orientations of the ferrimagnetic nanocrystals result in a uniform magnetization along the chains, enabling the cell to swim parallel to the Earth’s magnetic field. Figure adapted from SIMPSON et al. (2005).

MANN, S. (2001): Biomineralization: Principles and concepts in bioinorganic materials chemistry. Oxford University Press, Oxford, 198 pp. SIMPSON, E.T., KASAMA, T., PÓSFAI, M., BUSECK P.R., HARRISON, R.J., DUNIN-BORKOWSKI, R.E. (2005): J. Phys. Conf. Ser., 17, 108-121.