07.12.2012 Views

Mineralogie-Geochemie Institut für Geowissenschaften - Albert

Mineralogie-Geochemie Institut für Geowissenschaften - Albert

Mineralogie-Geochemie Institut für Geowissenschaften - Albert

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

<strong>Mineralogie</strong>-<strong>Geochemie</strong><br />

<strong>Institut</strong> <strong>für</strong> <strong>Geowissenschaften</strong><br />

<strong>Albert</strong>-Ludwigs-Universität Freiburg<br />

Annual<br />

Report<br />

2009


<strong>Institut</strong>e of Geosciences<br />

Mineralogy-Geochemistry<br />

<strong>Albert</strong>-Ludwigs-Universität Freiburg<br />

<strong>Albert</strong>straße 23b<br />

D-79104 Freiburg<br />

Germany<br />

Telephone: +49-761-203-6396<br />

Fax: +49-761-203-6407<br />

E-mail: info@minpet.uni-freiburg.de<br />

Wordwide web: http://www.minpet.uni-freiburg.de/


On the photograph (from left to right):<br />

Upper row: Hiltrud Müller-Sigmund, Reto Gieré, Jörg Keller, Ella Goldenberg, Kurt<br />

Bucher, Karin Eckmann, Melanie Schrage, Sebastian Weber, Peter Glasnák, Paul<br />

Keppner;<br />

Middle row: Wei Zhou, Fleurice Parat, Sigrid Hirth-Walther, Hoa Thi Bich Hoang,<br />

Xiaoyan Li, Ulrike Seelig, Slavica Drndelic-Eich, Dagmar Flemming (Lili), Kathleen<br />

Robinson, Isolde Schmidt;<br />

Lower row: Angela Thiemann, Christine Höher, Susanne Schuble, Anette von der Handt;<br />

Missing: Marlies Bergheim, Duy Ahn Dao, Juraj Majzlan, Anja Oehler, Sigrid Recha,<br />

Andreas Scheld, Tobias Weisenberger, Lu Zheng.<br />

Report editor: Fleurice Parat<br />

Cover photographs:<br />

1. Archean Pillow Lavas, Norway. Photo by Kurt Bucher<br />

2. Dr. Dao Duy Anh collecting a water sample from coal-mine drainage water at Cam<br />

Pha, Quang Ninh Province, Vietnam (December 2009)<br />

Top and bottom: Gabbro contact back veins, Norway. Photo by Kurt Bucher


Director’s Statement<br />

The year 2009 was the first full year of the new <strong>Institut</strong>e<br />

of Geosciences. The daily routine at the <strong>Institut</strong>e has not<br />

changed much. A few additional board meetings became<br />

necessary but the overall damage is rather limited.<br />

The most important event in 2009 was the final<br />

decision by the rectorate not to establish a professorate in<br />

hydrogeology and geothermal energy research. This means<br />

that the planning of future developments in the Geosciences<br />

of Freiburg became obsolete. The common focus on<br />

Kurt Bucher<br />

“geothermal energy utilization” in research and teaching<br />

has united the different fields in the geosciences after fall 2005. This is now history<br />

and the research and teaching profile of the Geosciences in Freiburg is characterized<br />

by five unrelated specialties represented by the research interests of the five remaining<br />

professorates.<br />

There are still two unfilled professorates at the Geosciences (in Geology and<br />

Crystallography) (as in 2005, 2006, 2007, and 2008). One of these positions (structural<br />

geology) is in the formal process of being filled. The present status is that the position has<br />

been offered to the top candidate. We hope that the person accepts the offer. The status<br />

of the second position is unclear. The original plan to establish a “hydrogeology and<br />

geothermal energy” professorate in order to support student demands and the job market<br />

has not been accepted by the rectorate.<br />

Mineralogy and Geochemistry as a part of the <strong>Institut</strong>e of Geosciences has been<br />

prosperous as ever. MG stands for well over 2/3 of the research production of the <strong>Institut</strong>e<br />

(the other 1/3 is contributed by Crystallography). In addition to the research production, in<br />

2009 four PhD’s graduated, two of them from MG Freiburg, one from Peking University<br />

and one from China University of Petroleum Qingdao. I am extremely happy about the<br />

rapidly increasing number of PhD from the MG. Particularly remarkable is the increasing<br />

number of excellent students from Eastern Asia at our <strong>Institut</strong>e (3 of four completed PhD).<br />

There were many changes to the staff in 2009. Dr. Juraj Majzlan finished his term<br />

as a research assistant at MG and assumed a full professor position at the University of<br />

Jena. Juro has been an excellent staff member and MG very gratefully acknowledges his<br />

outstanding efforts and achievements in research and teaching, which added substantially<br />

to the success of MG. Juro has been replaced by Anette von der Handt who joined us<br />

from Hawaii, where she spent a post doc position after her PhD at MPI in Mainz. She has<br />

been working on the petrology of ultramafic rocks from Gakkel Ridge. Also in 2009 we<br />

filled the old lab position of Erika Lutz with Angela Thiemann. Angela joined us from<br />

the <strong>Institut</strong>e of Inorganic Chemistry. Our lab technician Mellie Schrage left for her baby<br />

permission and we have been lucky to find Paul Robert Keppner who replaces Mellie<br />

for one year. Lab technician Dagmar Flemming returned to MG after her one year baby<br />

permission on a 50% level. Peter Glasnak has taken over the other 50% of Dagmar’s<br />

position and hopes to complete his PhD in 2010.<br />

Kurt Bucher


Table of Contents<br />

Teaching and Student Affairs................................................................................5<br />

Bachelor and Master program.....................................................................5<br />

Student Recruitment ...................................................................................5<br />

Guest Lectures Presented at MGI in 2008 ..........................................................6<br />

Invited Lectures Presented by the MGI Staff .....................................................6<br />

Service to the Earth Science Community ............................................................6<br />

Editorial Responsibilities ...........................................................................6<br />

Peer Review Responsibilities......................................................................7<br />

Administrative Offices, Membership in Committees and Boards..............7<br />

Major Events (Openings, Meetings, Conferences).....................................8<br />

Short Courses .............................................................................................8<br />

Completed Theses....................................................................................................9<br />

Bachelor Theses ..........................................................................................9<br />

Diploma Theses ..........................................................................................9<br />

PhD Dissertations......................................................................................10<br />

MGI 2009 Publication List ..................................................................................11<br />

Peer-reviewed Journal Articles, Books, and Book Chapters ....................11<br />

Abstracts....................................................................................................12<br />

Awards.......................................................................................................13<br />

Research Abstracts...............................................................................................14<br />

Hydrochemistry and Geothermal Energy .................................................15<br />

Metamorphic and Igneous Petrology.........................................................23<br />

Environmental Geosciences......................................................................35<br />

Mineralogy and Geochemistry..................................................................38<br />

Laboratories of the MGI .....................................................................................43<br />

Public Outreach Activities...................................................................................48<br />

Student Field Trips...............................................................................................49<br />

4


Teaching and Student Affairs<br />

5


Guest Lectures Presented at MGI in 2009<br />

Dr. Inga Moeck, GFZ Potsdam<br />

Die Nutzung des Rotliegend zur geothermischen Stromerzeugung: Das<br />

Geothermieprojekt Groß Schönebeck im Nordostdeutschen Becken. Januar 26, 2009<br />

Prof. Dr. Ingo Sass, Dipl.-Ing. U. Burbaum<br />

Artesisches Grundwasser, Anhydrit und Karsterscheinungen im Konflikt mit<br />

Erdwärmesonden: Überlegungen zur Schadensursache im Fall Staufen im Breisgau.<br />

June 29, 2009<br />

Dr. Arjan Dijkstra, IGUN-Université de Neuchâtel<br />

Osmium isotopic mantle heterogeneity - A perspective from the field, with implications<br />

for geodynamics. December 07, 2009<br />

Invited Lecture Presented by the MGI staff<br />

The natrocarbonatite volcano Oldoinyo Lengai, Tanzania, Earth Science Colloquium<br />

University Basel, December 9, 2009, Jörg Keller<br />

Influence and record of volatiles in magma chambers: inference from mineral composition<br />

and phase equilibria – CRPG Nancy (France), March 25, 2009, Fleurice Parat<br />

Mineralogy of the atmosphere: characteristics and health impacts of particulate matter.<br />

Universität Innsbruck (Austria), ÖMG Lecture Tour; May 7, 2009, Reto Gieré<br />

Mineralogy of the atmosphere: characteristics and health impacts of particulate matter,<br />

Montanuniversität Leoben (Austria), ÖMG Lecture Tour; May 5, 2009, Reto Gieré<br />

Mineralogy of the atmosphere: characteristics and health impacts of particulate matter,<br />

Universität Wien (Austria), ÖMG Lecture Tour; May 4, 2009, Reto Gieré<br />

Neue geowissenschaftliche Daten <strong>für</strong> die Tiefengeothermie am Oberrheingraben. –<br />

GeoTherm – expo & congress, Offenburg, March 05, 2009, Ingrid Stober & M.<br />

Jodocy.<br />

Melt stagnation at ultraslow-spreading ridges, Steinmann-<strong>Institut</strong>, University of Bonn,<br />

November 05, 2009, Anette von der Handt<br />

Palmen und Nordpol: Als Geowissenschaftlerin in der Forschung, Kolloquium zur<br />

Berufsqualifikation, Steinmann-<strong>Institut</strong>, University of Bonn, June 8, 2009, Anette<br />

von der Handt<br />

Service to the Earth Science Community<br />

Editorial offices<br />

The international system of scientific journal publication of research data and results<br />

depends largely on the volunteered effort of editors and peers writing reviews and<br />

assessments. The MGI has carried a heavy burden for maintaining an international high<br />

standard publication system. Reto Gieré is member of the editorial board of Journal of<br />

Petrology (the highest standard petrology journal); Kurt Bucher is on the advisory board<br />

of Journal of Petrology and associate editor of the Journal Geofluids. Ingrid Stober is<br />

associate editor of Hydrogeology Journal. Jörg Keller is member of the editorial board of<br />

Journal of Volcanology and Geothermal Research (JVGR).<br />

6


Peer-Review Responsibilities<br />

Journals<br />

The members of the institute have invested considerable time and effort in reviewing<br />

research papers for the following international first class journals: American Journal of<br />

Science, American Mineralogist, Applied Geochemistry, Atmospheric Environment,<br />

Bulletin of Volcanology, Canadian Mineralogist, Chemical Geology, Environmental<br />

Science & Technology, European Journal of Mineralogy, Journal of African Earth<br />

Sciences, Journal of Metamorphic Geology, Journal Petrology, Journal of Volcanology<br />

and Geothermal Research, Fuel, Geochemical Journal, Geochimica Cosmochimica Acta,<br />

Geofluids, Geology, Lithos, Mineralogical Magazine, Science of the Total Environment<br />

and others.<br />

Grant-awarding bodies<br />

The experts of MGI have written assessment of grants proposals for Deutsche<br />

Forschungsgemeinschaft (DFG), Germany, Natural Sciences and Engineering Research<br />

Council of Canada, U.S. National Science Foundation (both research and equipment<br />

proposals), USA, <strong>Institut</strong> de Radioprotection et de Sûreté Nucléaire, France, FNSNF,<br />

NFR, and other granting agencies worldwide.<br />

Administrative offices<br />

Kurt Bucher is Vice-Dean of the Faculty of Chemistry, Pharmacy and Geosciences<br />

until October 2011. Kurt Bucher was Director of the ZEE Center of Renewable Energy<br />

(together with Prof. Oesten and Prof. Reindl) until summer 2009.<br />

Reto Gieré is the Dean of Student Affairs and a member the Research Evaluation<br />

Committee (since Oct. 2008) and Admission Committee for M.Sc Curricula (since Apr.<br />

2008), <strong>Albert</strong>-Ludwigs-Universität Freiburg, Faculty Steering Committee (since Oct.<br />

2008), Habilitation Committee, Graduate Committee, School of Chemistry, Pharmacy<br />

and Geosciences, <strong>Albert</strong>-Ludwigs-Universität Freiburg (since Oct. 2005), Search<br />

Committee for the Professorship “Structural Geology and Tectonics”, <strong>Albert</strong>-Ludwigs-<br />

Universität Freiburg (May-July 2009), Search Committee for the Professorship “Risques<br />

et Environnement”, Université de Haute-Alsace, Mulhouse, France (April-May 2009). He<br />

is also a book advisor for the Geological Society, London (since June 2005), and member<br />

of the subcommittee for the Pyrochlore Group, International Mineralogical Association,<br />

Commission on New Minerals and Mineral Names (since September 2008) and member<br />

of the Campus Representative for the Geological Society of America (since Mar. 2009).<br />

Jörg Keller is a member of the International Scientific Evaluation Committee for the<br />

2008-2010 Research Programmes of Italian INGV (National Insitute of geophysics and<br />

Volcanology - Istituto Nazionale di Geofisica e Vulcanologia (INGV) and Dipartimento<br />

della Protezione Civile (DPC/INGV), Scientific Council for VULCANIA, Parc Européen<br />

du Volcanisme, Auvergne, France, Leiter des Geologenarchivs der Geologischen<br />

Vereinigung e.V. in der Universitätsbibliothek Freiburg; Medal and Awards Commissions<br />

of IAVCEI.<br />

7


Major Events (Openings, Meetings, Conferences)<br />

GeoTherm, Offenburg 5.-6. February 2009<br />

The <strong>Institut</strong>e participated in this major German conference and exhibit in Geothermal<br />

Resources Utilization with lecture presentations (Prof. Stober and Prof. Henk) and a<br />

permanently manned booth (Prof. Henk and team).<br />

Short courses<br />

“Geothermal Energy Utilization” a continuous education course by FH-DGG held at<br />

GeoTherm Offenburg. March 4, 2009, organized by Prof. Dr. Ingrid Stober<br />

Lectures were given by:<br />

Kurt Bucher: “Geothermal Fluids”.<br />

Ingrid Stober: “Overview on Deep Geothermal Energy Utilization, geothermal Parameters<br />

and geothermal Techniques”.<br />

Short course: “Hydrogeology of hard rock aquifers” a continuous education course by<br />

FH-DGG held at MG University of Freiburg. October 15, 2009, organized by Prof. Dr.<br />

Ingrid Stober.<br />

Lectures were given by:<br />

Kurt Bucher: “Water-rock interaction”.<br />

Ingrid Stober: “Overview on hydrogeology of hard rock aquifers, hydraulic parameters<br />

and hydraulic techniques”.<br />

Prof. Dr. Bernhard Dold (Universidad de Concepción, Chile) taught a short course<br />

entitled “Acid Mine Drainage and Sustainability in Metal Mining”. This excellent and<br />

very interesting course, which took place from December 21-23, 2009, was attended by<br />

25 students and scientists, including seven participants from other institutions.<br />

Topics included: Sulfide oxidation in mining; Element cycles in mine waste<br />

environments; Strategies for the environmental management of mine waste; Strategies<br />

for optimization and development of metal recuperation in the metallurgical process<br />

for a more sustainable mining operation. The participants had the opportunity to obtain<br />

knowledge from a well-known expert and to learn how to tackle real-life environmental<br />

problems, such as those shown in the figure:<br />

8<br />

Dr. Dao Duy Anh collecting a water<br />

sample from coal-mine drainage water<br />

at Cam Pha, Quang Ninh Province,<br />

Vietnam (December 2009)


Bachelor Theses<br />

Baierl Michael : Mineralogy and geochemistry of xenoliths and host tephras from Mt.<br />

Briancon. Advisor:Parat; co-referee: Müller-Sigmund<br />

Bockholt Jan: Tracerversuche im Grundwassertestfeld Merdingen.<br />

Advisor: Bucher; co-referee: Käß<br />

Bruzek Peter: Zechstein Anhydrit - Radiometrie-Messungen an Bohrkernen des Zechstein<br />

Anhydrits. Advisor: Henk; co-referee: Bucher<br />

Etter Kilian: Geology and Geochemistry of “killer-Lakes” in Africa.<br />

Advisor: Gieré, co-referee: Parat<br />

Faißt Tobias: Ryolith von Diersburg. Advisor: Gieré; co-referee: Müller-Sigmund<br />

Fibich Stephan: Sources of Asian mineral dust and atmospheric chemistry in terms of air<br />

pollution in East Asian mega-cities. Advisor: Gieré; co-referee: Hoppe<br />

Haas Simon: Entstehung und Vorkommen von Wadflecken in Sandsteinen.<br />

Advisor: Müller-Sigmund, co-referee: Stein<br />

Hahmann Andreas: Diskussion verschiedener geologischer Gesteinsformationen als<br />

mögliche Endlager von hochradioaktiven Stoffen. Advisor: Stein; co-referee: Gieré<br />

Kleine Barbara: Volatiles in minerals of the Fish Canyon Tuff Dacite, Colorado, U.S.A..<br />

Advisor: Parat; co-referee: Müller-Sigmund<br />

Koch Stefan: Alpine Naturgefahren - Auslösung von Schneebrettlawinen.<br />

Advisor: Gieré; co-referee: Hübel (Wien)<br />

Lehner Florian: Geologie des Untergrunds in den deutschen Gebieten bei Jestetten.<br />

Advisor: Rahn; co-referee: Gieré<br />

Nedyalkova Latina: Grey and black obsidians from Lipari, Italy.<br />

Advisor: Parat; co-referee: Müller-Sigmund<br />

Radecke Daniel:Markierungsversuch mit Uranin und Kaliumchlorid im hydrogeologischen<br />

Testfeld Merdingen. Advisor: Bucher; co-referee: Käß<br />

Rucki Katharina: Methoden zur Probenentnahme von reduziertem und langsam<br />

fliessendem Wasser in der Grube Clara bei Oberwolfach.<br />

Advisor: Bucher; co-referee: Gieré<br />

Wagner Moritz: Mineralogy of tephra and lavas from Arenal volcano.<br />

Advisor: Parat; co-referee: Müller-Sigmund<br />

Zech Mikko Jens: Kompilation gesteinstechnischer Daten zu Steinbrüchen im<br />

Buntsandstein. Advisor: Müller-Sigmund; co-referee: Henk<br />

Diploma Theses<br />

Niklas Mundhenk: Alteration klastischer Sedimente durch CO 2 und CO 2 -reiche Lösungen<br />

im Mittelrheingebiet. Advisor: Reto Gieré & F. May (BGR Hannover)<br />

Ralph Bolanz: Large-area arsenic pollution in the Horna Nitra valley (Slovakia).<br />

Advisor: Juraj Majzlan<br />

Björn Brecht: Chemical and mineralogical inventory of the waste impoundment in<br />

Pezinok (Slovakia). Advisor: Juraj Majzlan<br />

Sakonvan Chawchai: Mineralogy and Weathering of Antimony Deposits in the Black<br />

Forest”. Advisor: Reto Gieré and Andreas Danilewsky<br />

Johannes Dick: Ore mineralization at the Lom and Male Zelezne deposits (Slovakia).<br />

Advisor: Juraj Majzlan<br />

9


Sebastian Hobler: Geology and mineralogy of the ore occurences in Mlynna Dolina<br />

(Slovakia). Advisor: Juraj Majzlan<br />

Sebastian Lindauer: Jurassic manganese oxides deposits in Western Carpathians: A case<br />

study in Borinka. Advisor: Juraj Majzlan<br />

Ronny Müller: Ni-Co mineralization near Dobsina (Slovakia). Advisor: Juraj Majzlan<br />

Caroline Seeburger: Ore mineralization at Suggental Schwarzwald).<br />

Advisor: Juraj Majzlan<br />

Sven Thor: Bleiminerale in der Grube Clara und in Aufbereitungsprodukten.<br />

Advisor: Kurt Bucher<br />

Miryana Apostolova: Geothermie Bulgariens. Advisor: Kurt Bucher & Reto Gieré<br />

Radoslav Michallik: Mineralization at the Ag-Au veins Aller Heiligen and Rozalia in<br />

Hodrusa (Slovakia). Advisor: Juraj Majzlan<br />

PhD Dissertations<br />

Dao Duy Anh: Research of Technology of Manganese Ore Processing to Produce High<br />

Quality Finished Products such as EMD and CMD from Vietnam’s Manganese Ore.<br />

Advisor: Reto Gieré, co-referee: Kurt Bucher<br />

Weisenberger, Tobias: Zeolites on fissures of crystalline basement rocks.<br />

Advisor: Kurt Bucher; co-referee: Reto Gieré<br />

Zeng, Lu: Ultra-high-pressure ophiolites from Tian Shan, China.<br />

Advisor: Zhang Lifei, co-referee: Kurt Bucher<br />

Ahmatjan, Abdurahman: Fracture genesis of Ordovician carbonate rock in Tahe Oilfield<br />

Advisor: Zhong Jian Hua, co-referee: Kurt Bucher<br />

10


MGI 2009 Publication List<br />

Peer-reviewed Journal Article, Books, and Book Chapters<br />

Ackermann S., Gieré R., Newville M., Majzlan J., 2009: Antimony sinks in the<br />

weathering crust of bullets from Swiss shooting ranges. Science of the Total<br />

Environment 407, 1669-1682.<br />

Ackermann S., Armbruster T., Lazic B., Doyle S., Grevel K.-D., Majzlan J., 2009:<br />

Thermodynamic and crystallographic properties of kornelite (Fe 2 (SO 4 ) 3 ·~7.75H2O)<br />

and paracoquimbite (Fe 2 (SO 4 ) 3 ·9H 2 O). American Mineralogist 94, 1620-1628.<br />

Bratzdrum C., Grapes R., Gieré R., 2009: Late-stage hydrothermal alteration and<br />

heteromorphism of calc-alkaline lamprophyre dykes in Late Jurassic granite,<br />

Southeast China. Lithos 113, 820-830.<br />

Bucher K., Zhu Y., Stober I. 2009: Groundwater in fractured crystalline rock, the Clara<br />

mine, Black Forest, Germany. International Journal of Earth Sciences, 98, 1727-1739.<br />

Bucher K. & Grapes R. 2009: The Eclogite-facies Allalin Gabbro of the Zermatt-<br />

Saas Ophiolite,Western Alps: a Record of Subduction Zone Hydration. Journal of<br />

Petrology, 50, 1405-1442.<br />

Bucher K., Zhang L., Stober I. 2009: A Hot Spring in Granite of the Western Tianshan,<br />

China. Applied Geochemistry, 24, 402-410.<br />

Gieré R., Williams C.T., Wirth R., Ruschel K., 2009: Metamict fegusonite-(Y) in a<br />

spessartine-bearing granitic pegmatite from Adamello, Italy. Chemical Geology 261,<br />

333-345.<br />

Grapes R. & Keller J., 2009: Rhönite in undersaturated alkaline basaltic rocks, Kaiserstuhl<br />

Volcanic Complex, Upper Rhine Graben, SW Germany. European Journal of<br />

Mineralogy (accepted and in print 2009).<br />

Gertisser R., Preece K., Keller J., 2009: The Plinian Lower Pumice 2 Eruption, Santorini,<br />

Greece: Magma Evolution And Volatile Behaviour. Journal of Volcanology and<br />

Geothermal Research 186, 387-406.<br />

Grevel K.-D. & Majzlan J., 2009: Internally consistent thermodynamic data for<br />

magnesium sulfate hydrates. Geochimica et Cosmochimica Acta 73, 6805-6815.<br />

Hiller E., Jurkovic L., Kordík J., Slaninka I., Jankulár M., Majzlan J., Göttlicher J.,<br />

Steininger R., 2009: Arsenic mobility from anthropogenic impoundment sediments -<br />

consequences of contamination to biota, water and sediments, Poša, Eastern Slovakia.<br />

Applied Geochemistry 24, 2175-2185.<br />

Jankulár M., Hiller E., Jurkovic L., Veselská V., Majzlan J., 2009: Arsenic and zinc<br />

in impoundment materials and related stream sediments from a polluted area in<br />

eastern Slovakia: Distribution, mobility, and water quality. Journal of Hydrology and<br />

Hydromechanics 57, 200-211.<br />

Jodocy, M. & Stober, I., 2009: Geologisch-geothermische Tiefenprofile <strong>für</strong> den<br />

südwestlichen Teil des Süddeutschen Molassebeckens. Z. Dt. Ges. Geowiss., 160/4,<br />

359-366.<br />

Lü Z., Zhang L., Du J., Bucher K., 2009: Petrology of coesite-bearing eclogite from<br />

Habutengsu Valley, western Tianshan, NW China and its tectonometamorphic<br />

implication. Journal of metamorphic Geology, 27, 773-787.<br />

Majzlan J., 2009: Ore mineralization at the Rabenstein occurrence near Banská Hodruša,<br />

Slovakia. Mineralia Slovaca 41, 45-54.<br />

Parat F., Holtz F., René M., Almeev A., 2009: Experimental constraints on ultrapotassic<br />

magmatism from the Bohemian Massif (Durbachite series, Czech Republic).<br />

11


Contributions to Mineralogy and Petrology DOI : 10.1007/s00410-009-0430-5.<br />

Song S.G., Niu Y.L., Zhang L.F., Bucher K., 2009: The Luliangshan garnet peridotite<br />

massif of the North Qaidam UHPM belt, NW China - a review of its origin and<br />

metamorphic evolution. Journal of metamorphic Geology, 27, 621-638.<br />

Stober I. & Jodocy M., 2009: Eigenschaften geothermischer Nutzhorizonte im badenwürttembergischen<br />

und französischen Teil des Oberrheingrabens.- Grundwasser<br />

Grundwasser, 14, S.127-137, Springer-Verlag.<br />

Stober I., Fritzer T., Obst K., Schulz R., 2009: Nutzungsmöglichkeiten der Tiefen<br />

Geothermie in Deutschland.- BMU (Bundesministerium <strong>für</strong> Umwelt, Naturschutz<br />

und Reaktorsicherheit), 73 S., Berlin.<br />

Weisenberger T. & Spürgin S., 2009: Zeolites in alkaline rocks of the Kaiserstuhl<br />

volcanic complex, SW Germany - new micropobe investigation and their relationship<br />

to the host rock. Geolgica Belgica 12/1-2, 75-91<br />

Wiedenmann D., Zaitsev A.N., Britvin S.N., Krivovichev S.V., Keller, J., 2009:<br />

Alumoåkermanite, (Ca,Na) 2 (Al,Mg,Fe 2+ )(Si 2 O 7 ), a new mineral from the active<br />

carbonatite-nephelinite-phonolite volcano Oldoinyo Lengai, Northern Tanzania.<br />

Min. Mag. 73, 373-384.<br />

Zaitsev A.N., Keller J., Billström K., 2009: Isotopic composition of Sr, Nd and pb in<br />

unaltered natrocarbonatite and in pirssonite, shortite and calcite carbonatites from<br />

Oldoinyo Lengai Volcano, Tanzania. Doklady Earth Sciences, 425, 2, 302-306.<br />

Zaitsev A.N., Zaitseva O.A., Buyko A.K., Keller J., Klaudius J., Zolotaev A.A., 2009:<br />

Gem-quality yellow-green haüyne from Oldoinyo Lengai volcano, Northern Tanzania.<br />

Gems & Gemology, Vol. 45, No.3, 1-5.<br />

Ziegler S., Ackermann S., Majzlan J., Gescher J., 2009: Matrix composition and<br />

community structure analysis of a novel bacterial pyrite leaching community.<br />

Environmental Microbiology 11, 2329-2338.<br />

Abstracts<br />

Dietze V., Kaminski U., Oehler A., Gieré R., Stille P., Grobéty B., 2009: Einsatz und<br />

Absicherung der bildanalytischen Auswertung (dp>2.5 μm) von Passivsammlerproben<br />

im Rahmen einer trinationalen Zusammenarbeit mit chemischen und<br />

elektronenmikroskopischen Verfahren. Accepted 44. Messtechnisches Kolloquium,<br />

Goslar, June 2009.<br />

Dietze V., Kaminski U., Oehler A., Gieré R., Stille P., Grobéty B., 2009: Passive sampling<br />

technique Sigma-2, operational application and validation of the automated optical<br />

single-particle analysis in the size range 2.5–80 μm. International Conference on<br />

“Measuring Air Pollutants by Diffusive Sampling and Other Low Cost Monitoring<br />

Techniques”, Krakow. Abstract Volume, O18.<br />

Ghobadi M., Gerdes A., Brey G., Keller J., 2009: Trace element disribution in perowskite<br />

& pyrochlore of Kaiserstuhl sövite carbonatites. Abstract DMG 2009, Hallesches<br />

Jahrbuch <strong>für</strong> <strong>Geowissenschaften</strong> 31, p. 79.<br />

Gieré R., Rumble D., Günther D., Connolly J.A.D., 2009: Correlation of growth and<br />

breakdown of major and accessory minerals in metapelites from the Central Alps.<br />

Geological Society of America, Abstracts with Programs 41/7, p. 357.<br />

Gieré R., Chawchai S., Danilewsky A., 2009: Mineralogical composition and weathering<br />

of the Sulzburg antimony deposit, Black Forest. Geological Society of America,<br />

Abstracts with Programs, 41/7, p. 330.<br />

12


Goldenberg E., Könczöl M., Gieré R., Grobéty B., Seidel A., Mersch-Sundermann V.,<br />

Gminski R., 2009: Influence of chemical composition, particle size and morphology<br />

on the cytotoxic and genotoxic effects of three black toner powders and their<br />

dimethylsulfoxide (DMSO) extracts in cultured human epithelial A549 lung cells<br />

in vitro. International Symposium on “Mineralogy, Environment and Health”, Paris.<br />

86-88.<br />

Hellebrand E., von der Handt A., Johnson K., Snow J.E., Liu C., Dick H.J.B., Hofmann<br />

A.W., 2009: Composition, distribution and properties of the Ultra-Depleted Mantle<br />

component. 19th Goldschmidt Conference, Davos, Switzerland.<br />

Oehler A., Gieré R., Grobéty B., Dietze V., 2009: Preliminary results from a study<br />

of coarse airborne particles >2.5 μm in Hanoi, Vietnam. Goldschmidt Conference<br />

Abstracts, A963.<br />

Oehler A., Gieré R., Stille P., Grobéty B., Dietze V., 2009: Geochemical and mineralogical<br />

study of airborne particulate matter in Strasbourg, France. International Symposium<br />

on “Mineralogy, Environment and Health”, Paris. Abstract Volume, 38-39.<br />

Parat F. & Bucher K., 2009: Topaz-fluorite granites from the Black Forest, Germany:<br />

evolution of F-rich felsic magmas and origin of topaz. Goldschmidt conference,<br />

Davos. A992.<br />

Parat F., 2009: Sulphur yield of volcanic eruptions. Tag der Forschung, Fakultät <strong>für</strong><br />

Chemie, Pharmazie und <strong>Geowissenschaften</strong>, Universität Freiburg.<br />

Snow J.E., Ohara Y, Harigane Y., Michibayashi K., Hellebrand E., von der Handt A.,<br />

Loocke M., Ishii T., 2009: Secular evolution of partial melting and melt stagnation<br />

during the formation of Godzilla Mullion, Philippine Sea. T33D-07.<br />

von der Handt A., Hellebrand E., Snow J.E., 2009: Melt stagnation at ultraslow-spreading<br />

ridges - Tag der Forschung, Fakultät <strong>für</strong> Chemie, Pharmazie und <strong>Geowissenschaften</strong>,<br />

Universität Freiburg (published on website).<br />

Weber S. & Braun I., 2009: Petrological investigations and Electron microprobe analysis<br />

(EPMA) of rocks from the Palghat-Cauvery lineament, southern India. DMG Tagung,<br />

Halle-Wittenberg.<br />

Wiedenmann D., Keller J., Zaitsev A.N., 2009: Occurrence and compositional variation<br />

of high-Na-Al melilites at Oldoinyo Lengai, Tanzania. Abstracts XXVI International<br />

Conference “Geochemistry of Magmatic Rocks / School Geochemistry of Alkaline<br />

Rocks”, May 2009, Moscow.<br />

Zaitsev A.N. & Keller J., 2009: Mineralogy of carbonatites from active Oldoinyo Lengai<br />

volcano, Tanzania. Abstracts of V International Symposium “Mineral Diversity,<br />

Research and Preservation”, October 2009, Sofia, 66.<br />

Zaitsev A.N., Keller J., Jones G., Grassineau N., 2009: Mineralogical and geochemical<br />

changes of natrocarbonatites due to fumarolic activity at Oldoinyo Lengai volcano,<br />

Tanzania. Abstracts of XXVI International Conference “Geochemistry of Magmatic<br />

Rocks / School Geochemistry of Alkaline Rocks”, May 2009, Moscow, 168-169.<br />

Awards<br />

4th Most Cited Paper (Gieré & Sorensen 2004) in Reviews in Mineralogy and<br />

Geochemistry. GeoScienceWorld, January 2009<br />

(http://rimg.geoscienceworld.org/reports/mfc1.dtl)<br />

5th Most Cited Paper (Gieré & Sorensen 2004) in Reviews in Mineralogy and<br />

Geochemistry. GeoScienceWorld, February, March, April, May, June, July, August,<br />

September, October, November, December 2009<br />

(http://rimg.geoscienceworld.org/reports/mfc1.dtl)<br />

13


Research Abstracts<br />

14


Hydrochemistry and Geothermal Energy<br />

In 2009, we prepared a general invited article for the 10 year anniversary of the Journal<br />

“Geofluids” Bucher, K. and Stober, I. 2010. Fluids in the upper continental crust. Geofluids,<br />

14 pages. The paper will be a contribution to a collection of papers from leading<br />

scientists in the field of geofluids. The contributions will also be published as a hard cover<br />

book in early 2010.<br />

Hydrochemical evolution of deep groundwater in fractured basement aquifer<br />

The project studies a unique set of water<br />

samples from the world longest railroad<br />

tunnel currently under construction between<br />

Erstfeld and Bodio in Switzerland (NEAT<br />

Alptransit, Gotthard). The Amsteg section<br />

has been completed in 2006 and Ulrike<br />

Seelig used the Amsteg water samples<br />

for her PhD work. She has submitted her<br />

thesis at the end of December 2009 and<br />

will defend the thesis early in 2010. The<br />

revision of a first paper: “Seelig, U. and<br />

Bucher, K. Halogens in water from the<br />

crystalline basement of the Gotthard rail<br />

base tunnel (Central Alps)” has been resubmitted<br />

to Geochimica Cosmochimica<br />

Acta in December 2009. The manuscript<br />

of a second paper: “Seelig, U. and Bucher,<br />

K. Geochemical characterization of highpH<br />

waters from the crystalline basement of<br />

the new Gotthard rail tunnel, Switzerland,<br />

has been prepared and will be submitted to<br />

“Chemical Geology” in January 2010.<br />

Sedrun section, preparing for hydraulic<br />

test<br />

In 2009 we visited the Sedrun section<br />

two times and we collected water samples<br />

15<br />

from the Gotthard massif. The year 2010<br />

will be the final year with water samples<br />

from the Gotthard tunnel. The Faido and<br />

the Sedrun team will meet in the late fall<br />

2010 and then the tunnel construction work<br />

will not produce water and rock samples.<br />

Alptransit geologist Federico Giovanoli<br />

taking water sample<br />

Sedrun preparing for water sampling<br />

We received and analyzed the last water<br />

samples from the Erstfeld construction<br />

site in 2009. This section is completed and<br />

the complete set of data from the Erstfeld<br />

section awaits investigation.<br />

The NEAT Gotthard tunnel project will


continue to be our central research effort in the field of water and geothermal energy<br />

research.<br />

Geochemical characterization of high-pH waters from the crystalline basement of<br />

the new Gotthard rail tunnel, Switzerland<br />

Report by Ulrike Seelig<br />

122 water samples, collected from<br />

fractures in the Amsteg section of the new<br />

Gotthard railway tunnel, currently under<br />

construction in Switzerland, were analyzed<br />

and characterized according to their main<br />

element composition. The waters are<br />

characterized by their sodium domination<br />

and low to very low concentration of<br />

calcium and magnesium, respectively with<br />

varying dominance and concentration of<br />

the anions as shown in the ternary diagram<br />

in Fig. 1. In addition, they have very high<br />

fluoride concentration up to 29 mg/L and<br />

high pH values up to 10.4. According to<br />

the main element contribution to the total<br />

load of dissolved solids the tunnel waters<br />

can be categorized into the following six<br />

water types: Na HCO 3 -(Cl), Na Cl-(SO 4 ),<br />

Na Cl, Na HCO 3 , Na-(Ca) HCO 3 -SO 4 , and<br />

Ca-(Na) SO 4 .<br />

Stable isotope composition of H and O<br />

as well as geothermometrical calculations<br />

suggest a meteoric origin of the waters.<br />

Intensive water-rock interaction are solely<br />

responsible for the generation of these<br />

unique waters. The lithologies, where the<br />

waters were sampled from, are situated<br />

in the Aar massif in the Central Alps<br />

and consists of crystalline rocks with<br />

predominantly granitic character regarding<br />

their mineralogical content. The rocks<br />

have generally a similar mineralogical<br />

composition but with differing quantities<br />

and varying occurrences of minor<br />

minerals. In general, albite dissolution,<br />

leaching of fluid inclusions, sulphide<br />

oxidation, the alteration of F-phlogopite<br />

to F-free chlorite, and the formation of<br />

new Ca-bearing minerals were found<br />

as main overall reactions to form the<br />

16<br />

Gotthard tunnel waters. They, therefore,<br />

account as source for the majority of<br />

the components released into the tunnel<br />

waters. The reactions are in agreement<br />

with mineralogical findings in thin sections<br />

and on fracture walls. They could also be<br />

reproduced with mass balance models,<br />

where a surface water analysis, the tunnel<br />

water samples, and the mineralogical<br />

composition of the tunnel rocks served as<br />

input parameters. These models together<br />

with microscopic and EMP investigations<br />

revealed that small differences in the<br />

amounts of minerals reacting, varying<br />

environmental parameters such as P CO2 , as<br />

well as the involvement of certain minor<br />

minerals in the interactions are responsible<br />

for the formation of the six different water<br />

types.<br />

0.2<br />

0<br />

1<br />

Total<br />

alkalinity<br />

0.4<br />

0.6<br />

e<br />

d<br />

0.8<br />

SO4 0<br />

1<br />

a<br />

southern part of Amsteg section northern part of Amsteg section<br />

> Tm 12000 < Tm 12000<br />

0.2<br />

0.4<br />

0.8 0.6 0.4 0.2<br />

f<br />

b<br />

0.6<br />

0.8<br />

c<br />

1<br />

0<br />

Cl<br />

Ternary plot of major anions. Water<br />

samples are plotted according to their<br />

lithologies. Dashed line separates samples<br />

into northern (filled symbols) and southern<br />

(outlined symbols) part of the tunnel<br />

section by means of their Cl concentration.


Zeolites in fissures of crystalline basement rocks<br />

Our Zeolite Project focuses on zeolite minerals from Alpine fissures in crystalline<br />

basement rocks of the Swiss Alps. The topics of the project include: a complete review of<br />

Alpine zeolites, their geological and spatial distribution, the conditions and mechanisms<br />

of formation of zeolites in the diverse geological settings and the quantitative modeling<br />

of the fluid-rock interaction during the cooling of the basement units. Co-worker on the<br />

project was Tobias Weisenberger. He completed his PhD program in July 2009. A part of<br />

the thesis has been submitted as a paper manuscript to Journal of metamorphic Geology<br />

and is accepted for publication pending some major revisions. Below is the abstract of<br />

the paper:<br />

Zeolites in fissures of granites and gneisses of the Central Alps<br />

Tobias Weisenberger and Kurt Bucher<br />

Six different Ca-zeolites occur<br />

widespread in various assemblages in<br />

late fissures and fractures in granites and<br />

gneisses of the Swiss Alps. The zeolites<br />

form as a result of water-rock interaction<br />

at relatively low temperatures (< 250°C) in<br />

the upper continental crust. The low-grade<br />

fissure mineral assemblages are the key to<br />

the appreciation of water-rock interaction<br />

in hydrothermal and geothermal systems<br />

located in granites and gneisses of<br />

the crystalline basement. The zeolites<br />

typically overgrow earlier minerals of<br />

the fissure assemblages, but zeolites also<br />

occur as single stage fissure deposits in<br />

granite and gneiss. They represent the<br />

most recent fissure minerals formed<br />

during uplift and exhumation of the Alpine<br />

orogen. A systematic study of zeolite<br />

samples showed that the majority of finds<br />

originate from three regions particularity<br />

rich in zeolite-bearing fissures: (1) in the<br />

central and eastern part of the Aar- and<br />

Gotthard Massif, including the Gotthard<br />

road tunnel and the Gotthard-NEAT<br />

tunnel, (2) Gibelsbach/Fiesch, in a fissure<br />

breccia between Aar Massif and Permian<br />

sediments, and (3) in Penninic gneisses of<br />

the Simano nappe at Arvigo (Val Calanca).<br />

The excavation of tunnels in the Aar-<br />

and Gotthard massif give an excellent<br />

overview of zeolite frequency in Alpine<br />

17<br />

Laumontite cover on fissure quartz<br />

fissures, whereas 32% (Gotthard NEAT<br />

tunnel, 12000-18555) and 18% (Gotthard<br />

road tunnel) of all fissures are filled<br />

with zeolites. The number of different<br />

zeolites is limited to 6 species: laumontite,<br />

stilbite and scolecite are abundant and<br />

common, whereas heulandite, chabazite<br />

and epistilbite occur occasionally. Ca is<br />

the dominant extra-framework cations,<br />

with minor K and Na. Heulandite and<br />

chabazite additionally contain Sr up to<br />

29 and 10 mole%, respectively. Na and K<br />

content of zeolites tends to increase during<br />

growth as a result of systematic changes<br />

in fluid composition and/or temperature.<br />

The K enrichment of stilbite found in<br />

surface outcrops compare to stilbite in<br />

the subsurface may indicate late cation


exchange during interaction with surface<br />

water. Texture data, relative age sequences<br />

derived from fissure assemblages and<br />

equilibrium calculations shows that the Cadominated<br />

zeolites precipitated from fluid<br />

with decreasing temperature in the order<br />

(old to young = hot to cold): scolecite,<br />

laumontite, heulandite, chabazite and<br />

stilbite.<br />

The components necessary for zeolite<br />

formation are derived from dissolving<br />

primary granite and gneiss minerals. The<br />

nature of these minerals depends on the<br />

metamorphic history of the host rock.<br />

Zeolites in the Aar Massif derived from the<br />

dissolution of epidote or calcite and albite<br />

that were originally formed during Alpine<br />

greenschist metamorphism. Whereas<br />

albitization of plagioclase in higher grade<br />

18<br />

rocks releases the necessary components<br />

for zeolite formation, a process that<br />

is accompanied by a distinct porosity<br />

increase. Zeolite fissures occur in the zone<br />

where fluid inclusions in earlier formed<br />

quartz contain H 2 O dominated fluids. This<br />

is consistent with equilibrium calculations<br />

that predict a low CO 2 tolerance of<br />

zeolite assemblages particularly at low<br />

temperature. Pressure decrease along<br />

the uplift and exhumation can increase<br />

zeolite stability. The major zeolite forming<br />

reaction consumes calcite and albite; it<br />

increases pH and the total of dissolved<br />

solids. The produced Na 2 CO 3 waters are<br />

in accord with reported deep groundwater<br />

(thermal water) in the continental crust,<br />

which are typically oversaturated with<br />

respect to Ca-zeolites.<br />

Chemical Evolution of Surface Waters in Alpine Catchments of the Zermatt-<br />

Matterhorn Area (Central Alps)<br />

This project started in October 2007. The project will lead to the doctoral dissertation<br />

of Zhou Wei. In 2009 we concluded water sampling and analysis of surface waters in<br />

the Zermatt area. Currently, the data are summarized and discussed in a paper with the<br />

title “Wei Zhou and Kurt Bucher. Origin of solutes in surface waters from high Alpine<br />

catchments, Zermatt area (Swiss Alps)” scheduled for 2010.<br />

Field work carried out in the fall 2009 for the project focused on the description and<br />

the collection of weathering rinds on various rock types of the Zermatt area:<br />

Weathering of rock surfaces in the Zermatt-Saas area, quantification of water-rock<br />

interaction.<br />

Report by Zhou Wei<br />

Current research on water-rock<br />

interaction develops the quantitative<br />

approach to interpret the geochemical<br />

reactions and transport of solutes as coupled<br />

phenomena. In last two years, we have<br />

studied on the chemical composition of<br />

surface waters in high Alpine catchments,<br />

Zermatt-Matterhorn area. In those first<br />

results of our research project, the surface<br />

water in study area is predominantly<br />

controlled by the interaction of meteoric<br />

water with the exposed rocks (Fig. 1 &<br />

Fig. 2). Dissolving primary minerals of<br />

the predominantly metamorphic rocks<br />

contribute to the observed increase of total<br />

dissolved solids relative to precipitation<br />

leaving behind a residue of insoluble<br />

new minerals. In the following on the ongoing<br />

research process, we are interested<br />

in investigating the evolutions of primary


minerals and newly formed insoluble<br />

mineral, which are mainly forced by<br />

aqueous alteration or corrosion.<br />

Mineral dissolution and precipitation<br />

is controlled by the solubility of minerals<br />

at surface conditions in the presence of<br />

the atmosphere. Water-rock interactions<br />

proceeds until the surface water reaches<br />

saturation conditions with the most<br />

stable mineral assemblage. The geogene<br />

component of the chemical composition<br />

of most surface waters from catchments<br />

in silicate rock represents an intermediate<br />

non-equilibrium state shaped by mineral<br />

solubility and reaction rates. By linking<br />

a series of specified water compositions<br />

exhibit the combined effects of certain<br />

mineral dissolution one can deduce a<br />

19<br />

kinetically chemical model of geochemical<br />

reactions.<br />

The large variety of types of surface<br />

water compositions reflects the complex<br />

geology of the Zermatt area and the large<br />

variety of types of bedrocks that dominate<br />

individual catchments. In order to give<br />

a convincible water-rock interaction<br />

chemistry-weathering processing, during<br />

the field work in Autumn 2009 we collected<br />

most transformable and widely spreading<br />

rock in the area, including serpentinite,<br />

greenschist and gneiss. The streaky, rustcolored<br />

appearance and loosen texture<br />

of outcrops rock samples from Zermatt-<br />

Matterhorn area suggest that intense<br />

chemical weathering processes have acted<br />

upon it (Fig. 3).<br />

References<br />

Bearth, P. (1967) Die Ophiolithe der Zone von Zermatt-Saas Fee. Beiträge zur geologischen Karte der<br />

Schweiz N.F. Schweizerischen Geologischen Kommission. 132, pp.130.<br />

Bearth, P. (1953) 535 Zermatt. Geologischer Atlas der Schweiz. Schweizerischen Geologischen Kommission.<br />

Figure 1: The chemical type of surface water and lithology map in Findeln area (after<br />

Bearth, 1953, 1967).<br />

Figure 2: The chemical type of surface water and lithology map in Trockner Steg area<br />

(after Bearth, 1953, 1967).


Figure 3: BSE images of different altered rock types and the observation of thin sections<br />

under the microscopes .<br />

20


A Hot Spring in Granite of the Western Tianshan, China<br />

Kurt Bucher, Lifei Zhang, Ingrid Stober<br />

A cooperative project with scientists from Peking University, Beijing, PR China<br />

The study of the Muza Hot Spring is based on a research cooperation with Prof. Dr.<br />

Lifei Zhang from the Beijing University. The thermal water of the hot springs collected<br />

in 2005 at Muzhaerte in the Tian Shan range has been analyzed and studied in detail. The<br />

paper “A Hot Spring in Granite of the Western Tianshan, China” has been published in<br />

“Applied Geochemistry” in 2009. The paper abstract is printed below:<br />

The western Tianshan range is a major<br />

Cenozoic orogenic belt in central Asia<br />

exposing predominantly Paleozoic rocks<br />

including granite. Ongoing deformation is<br />

reflected by very rugged topography with<br />

peaks over 7000 m high. Active tectonic<br />

deformation is tied to an E-W trending<br />

fracture and fault system that sections the<br />

mountain chain into geologically diverse<br />

blocks that extend parallel to the orogen.<br />

In the Muzhaerte valley upwelling hot<br />

water follows such a fault system in the<br />

Muza granite. About 20 l min-1 Na-SO 4 -Cl<br />

water with a temperature of 55˚C having<br />

a total mineralization of about 1 g L-1<br />

discharge from the hot spring. The water is<br />

used in a local spa that is frequented by the<br />

people of the upper Ili river area. Its waters<br />

are used for balneological purposes and<br />

the spa serves as a therapeutic institution.<br />

The major element composition of<br />

the hot water is dominated by Na and by<br />

SO 4 and Cl, minor component is Ca. 1.04<br />

mmol L-1 dissolved silica corresponds to a<br />

quartz-saturation temperature of 116˚C and<br />

a corresponding depth of the source of the<br />

water of about 4600 m. This temperature<br />

is consistent with Na/K and Na/Li<br />

geothermometry. The water is saturated<br />

with respect to fluorite and contains 7.5<br />

mg L-1 F- as a consequence of the low Ca-<br />

Hot springs and salt lakes on the Tibet Plateau, China<br />

21<br />

concentration. The water is undersaturated<br />

with respect to the primary minerals of the<br />

reservoir granite at reservoir temperature<br />

causing continued irreversible dissolution<br />

of granite. The waters are oversaturated<br />

with respect to Ca-zeolite minerals (such<br />

as stilbite and mesolite), and it is expected<br />

that zeolites precipitate in the fracture pore<br />

space and in alteration zones replacing<br />

primary granite.<br />

The stable isotope composition of<br />

oxygen and hydrogen supports a meteoric<br />

origin of the water. The Cl/Br mass ratio<br />

of 1500 suggests that the salinity results<br />

from halite dissolution. Salts leached<br />

from powders of Muza granite show the<br />

same Cl/Br signature as the hot spring<br />

water. NaCl is stored in fluid and solid<br />

inclusions in the granite, which have<br />

been introduced to quartz by ductile<br />

shearing and faulting related to ongoing<br />

orogenesis. The hot water remobilizes<br />

the salt that is continuously liberated by<br />

the tectonic deformation. Water-granite<br />

interaction contributes a thenarditecomponent<br />

(Na 2 SO 4 ) to the major element<br />

composition by albite dissolution in<br />

sulfuric acid. The water-rock interaction<br />

along faults and fractures transforms and<br />

alters Muza granite to a low-temperature<br />

epigranite.<br />

Research cooperation with Prof. Dr. Zhong Jianhua from the University of Petroleum,<br />

Huangdao, Shandong Province has been established in 2005. In the summer 2006, we


visited the Qaidam basin and the Qaidam oilfields by invitation from Prof. Zhong and<br />

SINOPEC, the second largest Chinese oil company.<br />

During field work in 2006 on the northern Tibet plateau, we visited the oil fields, the<br />

salt deserts of the Qaidam basin and the Altun and Qilian mountains. We collected water<br />

samples from hot springs, salt lakes and tributaries to the lakes. In addition salt and rock<br />

samples were collected.<br />

In 2007, due to fortunate circumstances, we visited the DaQaidam hot springs again<br />

and re-sampled several outflow points. The new data are valuable additional information<br />

on the temporal variation of the hot spring system. The sampling campaign was made<br />

possible through the efforts of Prof. Zhang Lifei from Beijing University who also<br />

accompanied us in the field.<br />

In 2008, Prof. Zhong made it possible to visit western China in an exciting and<br />

outstanding field trip that brought us from Urumqi to Korla, Aksu and to Kashgar and<br />

from there via the Sinkiang-Tibet highway to Aksay Chin. The journey brought us via<br />

three mountain passes (two of them more than 5000 m) to the Tibet Plateau. The trip was<br />

difficult because of the riots in Lhasa and other parts of Tibet two month earlier that made<br />

it finally impossible to carry out our planned salt lake program.<br />

Fractures and fracture development in Ordovician carbonate reservoir rocks of<br />

Block 4, Tahe oil field, Tarim Basin, China<br />

Ahmatjan Abdurahman, Kurt Bucher, Jianhua Zhong<br />

This study is a part of the PhD project of Ahmatjan Abdurahman. Funding is provided<br />

by China Petrochemical Corporation (SINOPEC). Ahmatjan Abdurahman finished a<br />

research visit at the University of Freiburg in the spring 2009 and defended his PhD thesis<br />

December 22. 2009.<br />

The Tarim basin in Xingjiang is one of<br />

the most promising oil exploration areas<br />

in China. The Tahe oil field located at the<br />

Akekule uplift in the central Tarim basin<br />

is a prominent exploration block with<br />

an annual production capacity of oil and<br />

gas equivalent of more than 6 million<br />

tons. The capacity increases at the rate<br />

of 1-2 million tons per year. The Tahe<br />

oilfield is a carbonate karst reservoir and<br />

the porosity is mainly due to large karst<br />

cavities, pores and open fractures that<br />

resulted from karstification and tectonic<br />

deformation over several geologic periods.<br />

The complexity and heterogeneity of<br />

the reservoir is a serious challenge for<br />

exploration and development of the Tahe<br />

oilfield.<br />

22<br />

Fracture surveys were conducted across<br />

the Tahe oil field in order to investigate the<br />

development and geometries of fractures<br />

in carbonate reservoir rocks (Ahmatjan<br />

Abdurahman et al., 2008). The study<br />

shows that the fracture system and the<br />

internal morphology of these structures<br />

are very heterogeneous. Two kinds of<br />

fractures are dominating: tectoclase and<br />

sature. Satures are well developed in<br />

Tahe oil field, especially in carbonate<br />

karst reservoirs of Ordovician formations.<br />

Sature fracture frequency (fractures per<br />

meter) correlates well with hydrocarbon<br />

occurence, in contrast to tectoclase<br />

fractures. From the geometric relation<br />

between fracture and bedding plane, the<br />

sature can be classified into three types:


edding sature, oblique sature and vertical<br />

sature; also the tectoclase can be classified<br />

into three types: bedding fractures, oblique<br />

fractures and vertical fractures. Among<br />

them, bedding fractures are relatively<br />

rare. Tectoclase and satures combine<br />

to complex polygenic networks. Initial<br />

paths of hydrocarbon migration may have<br />

Metamorphic and Igneous Petrology<br />

23<br />

greatly enhanced the connectivity of the<br />

fracture network. Therefore, understanding<br />

fracture geometry, their syntactic relations<br />

and the contributing factors in fracture<br />

generation is compulsory for successful<br />

modeling hydrocarbon accumulation in<br />

fractured carbonate rocks.<br />

Zermatt-Saas Ophiolites, High-Pressure and Ultrahigh-Pressure Metamorphism<br />

The petrologic research in the Zermatt-Saas area that has started in 1978 with the<br />

mapping of the Matterhorn map sheet continued also in 2009. We published on the<br />

petrology of Allalin Gabbro (see below) and started a new PhD project on the petrology<br />

of eclogites and meta-sediments from previously unstudied outcrops in the ophiolite<br />

nappe. The new outcrops have been released by the retreating glaciers (thank’s to climate<br />

change). Sebastian Weber started with the new project in September 2009 with his first<br />

field season. His report follows below:<br />

Metapelites and eclogites from the Zermatt Ophiolite<br />

The P-T path of the HP-rocks from “Trockener Steg” region inside the Zermatt<br />

Ophiolites<br />

Sebastian Weber<br />

The Zermatt-Saas (ZS) unit represents<br />

an ophiolite complex in the western Alps<br />

situated between continental basement<br />

rocks of the Monte Rosa and Dent Blanche<br />

nappes. It remains the Piemonte Ligurian<br />

Ocean (Tethys) that opened in the Late<br />

Jurassic between the European continent<br />

to the NW and the Apulia plate to the<br />

SE. The rifting processes continues until<br />

the Mid-Cretaceous, when the Tethyian<br />

Ocean start to be subducted under its<br />

southern margin. The subduction process<br />

of the oceanic lithosphere was completed<br />

in the Eocene. The discovery of coesite in<br />

the Lago di Cignana unit that is part of ZS<br />

ophiolites is characterized an ultrahighpressure<br />

(UHP) terrain made it one of the<br />

most invastigated research objects of the<br />

alpine orogen.<br />

In this study we have taken samples<br />

from the “Trockener Steg” area, southwest<br />

of Zermatt that show characteristics<br />

comparable to the Lago di Cignana unit.<br />

The retraction of the glacier “Oberer<br />

Theodulgletscher” have generated new<br />

spectacular outcrops conditions in the<br />

last decade. These new exposed rocks<br />

show a heterogenous metamorphic unit of<br />

predominantly eclogites, but subordinary<br />

greenschist, metagabbros, serpentinites<br />

and metarodingites occur. The “Trockener<br />

Steg” eclogites are intercalated within<br />

biotite rich mica schist, which is in contrast<br />

to the classic Zermatt ophiolites. The mica<br />

schists does not belong to the ophiolitic<br />

unit and can be interpreted as a part of<br />

continental basement.<br />

The ongoing study will focus on the


following points by doing field work, phase<br />

modeling and geochemical investigation:<br />

(i) What is the relationship between<br />

the different lithologies, (ii) compare<br />

calculated P-T data from “Trockener<br />

Steg” rocks with the P-T data of the<br />

surrounding ophiolite units, (iii) search<br />

for signatures of UHP metamorphism, and<br />

(iv) investigate the geochemical signature<br />

to get informations about the protolithe.<br />

17 samples were taken in the late fall of<br />

2009 during fieldwork, including eclogite,<br />

garnet-phengite and biotite rich mica-<br />

schist. Nearly all of them were selected<br />

for thin section textural analyses. After<br />

this thin sections were investigated with<br />

the electron microprobe to determine the<br />

chemical composition of all mineral phases.<br />

By the occurrence of the paragenesis of<br />

omphacite, phengite and garnet, this rocks<br />

BSE images of eclogite sample 895<br />

24<br />

are well suited to calculate P-T conditions<br />

by using conventional thermobarometry<br />

and Theriak-Domino program. This<br />

high pressure assemblage is retrogressed<br />

to greenschist facies conditions. Here<br />

garnet is replaced at the rims by chlorite<br />

and biotite, whereas omphacite shows<br />

symplectites of actinolite and albite<br />

around the margins, as well as titanite and<br />

ilmenite overgrowth on rutile, caused by<br />

decompression.<br />

Some relicts of the prograde history<br />

can be found as inclusions in garnet and<br />

omphacite. Typical inclusions are epidote,<br />

glaucophane, quartz or rutile. Phengite<br />

has not been found as inclusions in other<br />

mineral grains, but occurs in the matrix,<br />

where it shows a preferred orientation<br />

parallel to the matrix foliation.<br />

In 2009 we published the paper on the petrology of the Allalin Gabbro in Journal of<br />

Petrology, 50, 1405-1442.<br />

The eclogite-facies Allalin gabbro of the Zermatt-Saas ophiolite, Western Alps: a<br />

record of subduction zone hydration<br />

Kurt Bucher and Rodney Grapes<br />

The Allalin gabbro is a 2 x 0.5 km block<br />

of layered olivine-gabbro and troctolite<br />

included in the Zermatt-Saas ophiolite<br />

nappe of the Western Alps. Comprehensive<br />

texture, mineral and rock composition data<br />

together with a thermodynamic analysis of<br />

the complex phase associations permit a<br />

detailed reconstruction of the igneous and<br />

metamorphic reaction history recorded<br />

by the gabbroic rocks. Based on rock<br />

and mineral composition data, the Allalin<br />

gabbro represents part of a Middle Jurassic


underplate of mafic magma at the base of the<br />

continental Apulian Plate (Dent Blanche<br />

- Sesia Lanzo system). Granulite facies<br />

recrystallization during cooling at ~825°C<br />

/ 1.0 GPa involving formation of Opx-Grt<br />

coronas between Ol-Pl can be related to<br />

crustal thickening. Eocene subduction of<br />

the Tethys oceanic lithosphere under the<br />

Apulian Plate detached the gabbro from<br />

the base of the continent and incorporated<br />

it into the ophiolite. Increasing pressure<br />

in the descending slab had little effect on<br />

the gabbro, which still locally contains<br />

unaltered igneous Ol, Aug and Pl and<br />

well preserved magmatic textures. With<br />

increasing subduction depth an increasing<br />

amount of aqueous fluid accessed the<br />

gabbro and transformed Pl to Zo-Jd-Ky-<br />

Tianshan Ophiolite, Xingjiang, Western China<br />

High-Pressure and Ultrahigh-Pressure Metamorphism<br />

25<br />

Qtz. At about 2.5 GPa (93 km) at ca. 610°C,<br />

a dramatic hydration process converted<br />

most of the rocks (>90 vol.%) into a fully<br />

hydrated eclogite-facies assemblage of<br />

Omp + Zo + Tlc + Cld ± Grt ± Ky + Rt.<br />

The full hydration under water-present<br />

conditions occurred at the greatest depth<br />

reached by the gabbro. After detachment<br />

from the downgoing slab, i.e. along the<br />

ascent path, Gln, Pg, and Mrg formed as<br />

additional hydrates. This last phase of<br />

hydration desiccated the metagabbro at a<br />

depth of ca. 78 km and from then on the<br />

rocks were essentially devoid of a free<br />

fluid phase. The Allalin gabbro confirms<br />

that the fundamental high-pressure<br />

transformation of mafic rocks is: gabbro +<br />

H 2 O = eclogite.<br />

This research project of Prof. Dr. Zhang Lifei of Peking University has been extended<br />

and receives funding for the next three years. The Tianshan UP and UHP ophiolites have<br />

specific similarities with the rocks of the Zermatt-Saas ophiolite. Therefore, a cooperative<br />

project involving both the Peking University and the University of Freiburg has been<br />

established in 2005. The cooperation produced joint research publications and we have<br />

been on jointly organized field trips in the Tianshan and Qilian mountains of China,<br />

the Alps and the Norwegian west coast. In 2009 Zeng Lü finished his 1.5 year visit in<br />

Freiburg and repurned to Beijing. He submitted his thesis in the late fall and defended his<br />

PhD thesis December 21. 2009 (I participated in the defense in Beijing). One subproject<br />

of the thesis has been published in 2009: Lü, Z., Zhang, L., Du, J. and Bucher K. 2009.<br />

Petrology of coesite-bearing eclogite from Habutengsu Valley, western Tianshan, NW<br />

China and its tectono-metamorphic implication. Journal of metamorphic Geology, 27,<br />

773-787. It is summarized below:<br />

Coesite-bearing eclogite from Habutengsu Valley, western Tianshan, NW China and<br />

its tectono-metamorphic significance<br />

Zeng Lü, Lifei Zhang, Jinxue Du and Kurt Bucher<br />

Coesite inclusions in garnet have<br />

been found in eclogite boudins enclosed<br />

in coesite-bearing garnet micaschist in<br />

the Habutengsu Valley, Chinese western<br />

Tianshan. The UHP mineral is distinguished<br />

from retrograde quartz by means of its<br />

optical characteristics, CL imaging and<br />

Raman analyses (Fig.1). The coesitebearing<br />

eclogite is mainly composed<br />

of porphyroblastic garnet, omphacite,<br />

paragonite, glaucophane and barroisite,<br />

minor amounts of rutile and dotted (or


Fig. 1 CL image showing the microtextures<br />

of SiO 2 aggregates. Inset photo was taken<br />

under plane polarized light.<br />

banded) graphite. In addition to coesite<br />

and quartz, the zoned porphyroblastic<br />

garnet contains inclusions of omphacite,<br />

Na-Ca amphibole, calcite, albite, chlorite,<br />

rutile, ilmenite and graphite. Multi-phase<br />

inclusions (e.g. Czo + Pg ± Qtz, Grt II +<br />

Qtz and Chl + Pg) can be interpreted as<br />

breakdown products of former lawsonite<br />

and possibly chloritoid. Coesite occurs<br />

scattered within a compositionally<br />

homogenous but narrow domain of garnet<br />

(outer core), indicative of equilibrium<br />

26<br />

at the UHP stage. Garnet-clinopyroxene<br />

thermometry yields peak temperatures of<br />

420-520°C at 2.7 GPa. Phase equilibrium<br />

calculations further constrain the P-T<br />

conditions for the UHP assemblage Grt +<br />

Omp + Lws + Gln + Coe to 2.4 - 2.7 GPa<br />

and 470-510°C (Fig. 2). Modeled modal<br />

abundances of major minerals along a 5°C<br />

km-1 geothermal gradient suggests two<br />

critical dehydration processes at ~430°C<br />

and ~510°C respectively. Computed<br />

garnet composition patterns are in good<br />

agreement with measured core-rim<br />

profiles.<br />

The petrological study of coesitebearing<br />

eclogite in this paper provides<br />

insight into the metamorphic evolution<br />

in a cold subduction zone. Together with<br />

other reported localities of UHP rocks<br />

from the entire orogen of Chinese western<br />

Tianshan, we conclude that the regional<br />

extent of UHP-LT metamorphism in<br />

Chinese western Tianshan is extensive<br />

and considerably larger than previously<br />

thought, although intensive retrogression<br />

has erased UHP-LT assemblages at most<br />

localities.<br />

Fig. 2 Phase modeling result for the coesite-bearing eclogite, with mineral assemblage<br />

(left) and garnet composition contouring (right).


In 2009 we also published a paper on the Luliangshan garnet peridotite body near<br />

DaQaidam. Song, S.G., Niu, Y.L., Zhang, L.F. and Bucher K. 2009. The Luliangshan<br />

garnet peridotite massif of the North Qaidam UHPM belt, NW China - a review of its<br />

origin and metamorphic evolution. Journal of metamorphic Geology, 27, 621-638. We<br />

visited the garnet peridotite body in the year 2007 during our field work in the North<br />

Qaidam and in the Qilian mountains. The garnet peridotite research is abstracted below:<br />

Ultrahigh-pressure garnet peridotites from Alaskan-type ultramafic cumulates in<br />

the North Qaidam UHPM belt, NW China<br />

The Luliangshan garnet peridotite<br />

massif is an ultramafic complex in the<br />

North Qaidam UHPM belt, NW China.<br />

The strongly layered complex comprising<br />

of garnet-bearing dunite, Grt-harzburgite,<br />

Grt-lherzolite and Grt-pyroxenite and<br />

garnet-free dunite occurs together with<br />

eclogite embedded in various continental<br />

gneisses. The geological setting, the<br />

internal structure, bulk-composition, REE,<br />

isotopic and mineral composition data<br />

show that the garnet peridotite derives<br />

from a middle Ordovician Alaskan-type<br />

layered sub arc cumulate intrusion of<br />

ascending mantle wedge melts. An abyssal<br />

peridotite protolith can be excluded.<br />

During the Ordovician-Silurian<br />

continental collision, thickening and<br />

foundering the Luliangshan peridotite<br />

complex has been exposed to ultrahigh<br />

pressures (UHP) reaching 5.5 GPa<br />

possibly > 6 GPa at temperatures of 900˚C<br />

(perhaps up to 1000˚C) corresponding to<br />

27<br />

a depth of about 200 km. The extreme<br />

pressure conditions have been derived<br />

from thermobarometry using mineral<br />

compositions of the garnet peridotite<br />

assemblages, but they are supported by a<br />

wealth of decompression-induced mineral<br />

exsolution in UHP minerals and by<br />

diamond inclusion in zircon.<br />

The Luliangshan garnet peridotite has<br />

experienced four stages of retrograde<br />

overprint during exhumation that lasted<br />

into the Devonian: I) decompressioninduced<br />

unmixing of the UHP minerals,<br />

II) garnet kelyphitisation, III) amphibole<br />

overprinting and IV) serpentinization.<br />

Hydrous minerals occurring within peak<br />

metamorphic assemblage represent<br />

pseudo-inclusions, that is reaction products<br />

of reactions related to various stages of<br />

decompression and cooling rather than<br />

prograde inclusions during porphyroblast<br />

growth.<br />

Fieldwork in the Luliangshan<br />

garnet peridotite body<br />

near DaQaidam


The Seiland Project in Northern Norway<br />

In 2009 we continued fieldwork in the Seiland Complex of Northern Norway. The<br />

project was initiated in the summer of 2003 and about 8 weeks of fieldwork have been<br />

performed. In 2009 an additional 7 weeks of field work produced the final collection of<br />

water samples from surface waters and an extensive collection of rock samples from the<br />

Seiland complex and its country rocks. 100 water analyses are now available from the<br />

Seiland area.<br />

The research project collected water and rock samples on Stjernøya, on Seiland<br />

and on the Øksfjorden peninsula, Northern Norway (70-71˚N). The Paleozoic alkaline<br />

igneous complex consists of e series of rocks that are characterized by high weathering<br />

rates. The rocks include nepheline-syenite, dunite, wherlite, carbonatite, troctolite and<br />

various gabbros including olivine gabbro. Fieldwork included detailed study of selected<br />

outcrops particularly in the nepheline-syenite mine of North Cape minerals on Stjernøy.<br />

The various occurrences of zeolite veins in the alkaline rocks and the gabbros are one<br />

of the main topics of the water-rock interaction research. Veins in the alkaline rocks<br />

contain thomsonite, natrolite and mesolite, in the gabbros laumontite dominates the vein<br />

assemblage. The field data and observations will be combined with water composition<br />

data and rock (mineral) data for an analysis of water-rock interaction in areas with rapidly<br />

weathering silicate rocks.<br />

Øksfjord gabbro complex<br />

Reinfjord peridotite<br />

28<br />

Li Xiaoyan started her PhD project in<br />

the Seiland Igneous Province and studied<br />

the petrology and geochemistry of the<br />

nepheline-syenite on Stjernøy. In addition<br />

during the field campaign 2009 she<br />

collected contact metamorphic gneisses in<br />

the aureole of the igneous complex. She<br />

is currently preparing a manuscript on<br />

the Ne-syenite and collects data from the<br />

high-grade gneisses.<br />

Xiaoyan and Zeng in the Stjernøy<br />

carbonatite


Magmatic and fluid evolution of nepheline syenite from the Seiland Igneous<br />

Province, Northern Norway<br />

Xiaoyan Li, Kurt Bucher<br />

The textures of the nepheline syenites<br />

from the Seiland Igneous Province<br />

(Northern Norway) indicate a slow<br />

isobaric cooling process involving an<br />

ortho-magmatic stage and a post-magmatic<br />

stage. The mineral assemblage of the orthomagmatic<br />

stage is clinopyroxene (saliteaugite)<br />

+ sanidine + nepheline + magnetite<br />

+ ilmenite + calcite at 750°C; sub-solidus<br />

radox reactions could be observed in<br />

textures (1) clinopyroxene surrounded<br />

by calcic amphibole (hastingsite and<br />

ferro-pargasite), and (2) ilmenite with<br />

titanite rim. In the cooling stage, the<br />

high temperature sanidine developed<br />

perthite texture, and nepheline crystals reequilibrated<br />

at a low temperature (< 500°C)<br />

suggested by the mineral chemistry.<br />

The latest autometasomatic alteration<br />

29<br />

extensively transferred nepheline into<br />

fibrous Na-zeolite (natrolite, thomsonite),<br />

and developed oligoclase rim and minor<br />

grossular when albitization happened<br />

along the boundary between perthite and<br />

other minerals. The development of this<br />

mechanism is reflected by several tiny<br />

veins (1-5mm wide) composed of zeolite<br />

aggregation and calcite, which accompany<br />

bilateral reaction zones displaying a<br />

remarkably reddish color. In addition,<br />

bulk chemical variations within reaction<br />

zones and original parts, combined with<br />

reactions, indicate a highly fractionated,<br />

volatile-rich fluid with low K/Na ratio<br />

(


Petrological investigations and Electron microprobe analysis (EPMA) of rocks from<br />

the Palghat-Cauvery lineament, southern India<br />

Sebastian Weber & Ingo Braun (Universität Bonn)<br />

Southern India exposes one of the major<br />

parts of east Gondwana, and comprises an<br />

accumulation of different tectonic blocks<br />

that assembled during different times of<br />

the Earth`s history. The oldest unit of these<br />

cratonic blocks is the Dharwar Craton (DC)<br />

that underwent initial growth during the<br />

Early Archean and was last consolidated<br />

at the end of the Archean c. 2,5 Ga ago.<br />

The terrains of the DC have not preserved<br />

any significant younger event. In contrast<br />

to this, Proterozoic blocks of the Southern<br />

Granulite Terrain (SGT) show strong<br />

imprints of the Pan-African (550-500 Ma)<br />

and, to the same extent, of Grenvillian<br />

high-grade metamorphism. In this study 23<br />

samples were taken from a c. 400 km large<br />

area in the eastern part of the transition<br />

zone between the DC in the north and the<br />

SGT in the south, the so called Palghat-<br />

Cauvery lineament, which is interpreted as<br />

a Proterozoic shear zone. The studied area<br />

lies west to the town of Erode, and mainly<br />

consists of highly deformed gneisses<br />

with intercalations of metabasites, BIF<br />

and other rock types. The common stable<br />

assemblage in the metabasites comprises<br />

quartz, hornblende, garnet, orthopyroxene,<br />

clinopyroxene and plagioclase and reflects<br />

granulite-facies metamorphism. The P-T<br />

evolution of these mafic granulites has<br />

been constrained with TWQ (version 2.02)<br />

and, yielded peak conditions of ~ 900°C<br />

and 10 +/- 1 kbar. These results correspond<br />

well with other P-T data from the literature<br />

(Srikantappa et al., 2003). Microtextures<br />

of BIF show spectacular pyroxeneplagioclase<br />

symplectites around garnet,<br />

which indicate a stage of decompression.<br />

30<br />

The application of TWQ to these rocks<br />

gave P-T data of 600 – 800 °C and 6 -<br />

8 kbar. Electron-microprobe (EPMA)<br />

dating of monazite has been applied to<br />

two gneiss samples. The monazite grains<br />

vary strongly in shape and size and only<br />

some of them show zonation. Determined<br />

monazite ages range between 706-331 Ma<br />

with a strong predominance of Pan-African<br />

ages between 550 – 500 Ma. These data<br />

support the available geochronological<br />

data that the last major tectonic-thermal<br />

event in the SGT took place during the<br />

Pan-African orogeny (Meissner et al.,<br />

2002). Because of their different lithology<br />

it is not possible to link the monazite ages<br />

with the P-T data from the metabasites. It<br />

therefore remains unclear if the P-T path<br />

estimated in the metabasites recorded<br />

archean event and subsequent overprinted<br />

during the Pan-African orogeny or if they<br />

can be correlated with the age data from<br />

the gneisses and thus reflect a Pan-African<br />

stage of high-grade metamorphism and<br />

decompression. We assume the textures<br />

inside the metabasites form during the<br />

archean and were preserved during the<br />

Pan-African event.<br />

References<br />

Meissner, B., Deters, P., Srikatappa, C., Kohler, H.,<br />

2002. Geochronological evolution of the Moyar,<br />

Bhavani and Palghat shear zones of southern India:<br />

implications for east Gondwana correlations.<br />

Precambrian Res. 114, 149–175.<br />

Srikantappa, C.,Srinivas, G., Basavarajappa, H.T.,<br />

Prakash-Narasimha, K.N., Basavalingu, B., 2003,<br />

Metamorphic Evolution and Fluid Regime in the<br />

Deep Continental Crust along the N-S Geotransect<br />

from Vellar to Dharapuram, Southern India,<br />

Memoir Geological Society of India, 50, 319-373.


Constraining the thermal architecture of Hole 1309D (IODP Leg 304/305) through<br />

geospeedometry<br />

Anette von der Handt, Eric Hellebrand*, Kevin Johnson* (*University of Hawaii)<br />

More than 70% of the Earth’s crust is<br />

formed along mid-ocean ridges. A key<br />

role in the formation of the oceanic crust<br />

is played by the presence and nature of the<br />

axial magma chamber. Several models are<br />

used to describe the architecture and timing<br />

of the crust formation along mid-ocean<br />

ridges. These include: (a) crystallisation<br />

in deep (20-30 km) magma chambers,<br />

leading to a high-pressure crystallisation<br />

signature in MORB with cooling largely<br />

due to subsequent uplift; (b) crystallisation<br />

in large shallow level intrusions that are<br />

emplaced episodically; (c) emplacement<br />

of many small (m-scale) shallow level<br />

intrusions that cool separately. These<br />

different models predict very different<br />

thermal histories; in the first case cooling<br />

will be slow due to the hot wall-rocks and<br />

cooling will be largely controlled by the<br />

uplift rate. In the latter models cooling rates<br />

will depend on the size of the intrusion,<br />

the thermal structure at shallow levels and<br />

the extent of hydrothermal cooling. Thus<br />

by determining the cooling rate of samples<br />

from the lower oceanic crust, we can test<br />

these different models. One important<br />

method for this approach is the Calciumin-olivine<br />

geospeedometer that is based<br />

on the down-temperature diffusion of Ca<br />

out of olivine into clinopyroxene. The<br />

31<br />

Ca content in olivine in equilibrium with<br />

clinopyroxene is strongly temperature<br />

dependent and only very weakly pressure<br />

dependent at the conditions in the oceanic<br />

crust.<br />

However, only a limited number of<br />

sites exists where continuous sections of<br />

lower crust could be sampled. The most<br />

important insight into the lower oceanic<br />

crust that we have today comes from<br />

long drill cores obtained during drilling<br />

programs such as the ODP and IODP<br />

programs. For this study, we focus on a<br />

sample site at the slow-spreading Mid-<br />

Atlantic Ridge at 30°N. Here, deep drilling<br />

of the domal core of Atlantis Massif<br />

during IODP Leg 304/305 obtained a 1.5<br />

km long, dominantly gabbroic core (Hole<br />

1309D). The common occurrence of fresh,<br />

undeformed, olivine in Hole 1309D allows<br />

the Ca-in-ol geospeedometer to be applied<br />

throughout the core. Here we show the<br />

results from a short interval that was<br />

chosen to test the potential of the Ca-inol<br />

geospeedometer to unravel the intrusion<br />

sequence at Hole 1309D.<br />

The chosen interval consists of<br />

dunitic troctolite in the upper half and<br />

olivine gabbro in the lower half with a<br />

diffuse contact in between. The lower<br />

olivine gabbro is further crosscut by a<br />

small gabbroic vein with sharp contacts.<br />

While the major element composition of<br />

olivine is highly variable (Mg-number:<br />

Downhole variation in Mg-number<br />

(=Mg/(Mg+Fe)) in olivine and cooling<br />

rates calculated from the Ca-in-olgeospeedometer<br />

for a short section in<br />

Hole 1309D, Atlantis Massif, 30°N<br />

Mid-Atlantic Ridge. Cooling rates<br />

increase toward contacts while major<br />

element composition of olivine is less<br />

systematic.


0.68-0.85), it shows no compositional<br />

difference between the small vein and the<br />

olivine gabbro unit it intruded.<br />

Cooling rates calculated from the Cain-ol-geospeedometer<br />

show increasing<br />

cooling rates toward contacts. Additionally,<br />

fastest cooling is seen by the small vein,<br />

in agreement with an intrusion at shallow<br />

levels. The Ca-in-ol geospeedometer<br />

32<br />

gives consistent results for several<br />

olivine grains that were analysed in<br />

each sample. We therefore conclude<br />

that this geospeedometric approach has<br />

the potential to determine the relative<br />

sequence of intrusive lithologies as well<br />

as the overall uplift history of Atlantis<br />

Massif.<br />

Topaz-fluorite granites from the Black Forest, Germany: evolution of F-rich felsic<br />

magmas.<br />

Fleurice Parat and Kurt Bucher<br />

F-bearing phases such as topaz,<br />

together with fluorite, micas and apatite,<br />

appear late in the crystallization history of<br />

granitic systems. Topaz crystallizes mostly<br />

from vapour, rather than melt, although<br />

questions of magmatic vs. hydrothermal<br />

origins of topaz are still debated because<br />

its parageneses and stability involves a<br />

large number of interrelated factors. The<br />

Black Forest area in the southwestern<br />

part of Germany is an ideal area to study<br />

the evolution of felsic magmas and the<br />

stability of topaz because topaz as well as<br />

other F-bearing phases such fluorite, micas<br />

and fluorapatite are present in variscan<br />

peraluminous granites and associated<br />

rocks (e.g. pegmatite, aplite).<br />

Topaz-biotite granite and biotitemuscovite<br />

granite (topaz-free) contain<br />

quartz, plagioclase, alkali feldspar,<br />

fluorite, fluorapatite (up to 5 wt.% F), and<br />

zircon. Topaz granite deviates in chemical<br />

composition markedly from topaz-free<br />

granite. This peraluminous high-SiO 2<br />

granite (A/CNK=1.11) is relatively rich<br />

in F (0.36 wt.%), and low in Mg, Fe and<br />

Ti. The trace element composition is<br />

characterized by anomalously high Rb<br />

and Nb, and by low Ba and Zr suggesting<br />

highly differentiated residual melts similar<br />

to other topaz-bearing granite. Topaz<br />

granite contains fluor-topaz (5 vol.%; 18.3-<br />

20.3 wt.% F) in the matrix as subhedral<br />

grain (up to 800 μm) and as inclusion in<br />

quartz and plagioclase. Fluorite is present<br />

as small crystal in the matrix (


Experimental constraints on ultrapotassic magmatism from the Bohemian Massif<br />

(Durbachite series, Czech Republic).<br />

Fleurice Parat, François Holtz 1 , Miloš René 2 , and Renat Almeev 1<br />

1 Leibniz Universität Hannover; 2 <strong>Institut</strong>e of Rock Structure and Mechanics, Praha<br />

The equilibrium phase relations of a<br />

mafic durbachite (53 wt.% SiO 2 ) from<br />

the Trebíc pluton, representative of the<br />

Variscan ultrapotassic magmatism of the<br />

Bohemian Massif (338-335 Ma), have been<br />

determined as a function of temperature<br />

(900-1100°C), pressure (100-200 MPa),<br />

and H 2 O activity (1.1 to 6.1 wt.% H 2 O<br />

in the melt). Two oxygen fugacity ranges<br />

were investigated: close to the Ni-NiO<br />

(NNO) buffer and 2.6 log unit above NNO<br />

buffer (∆NNO+2.6). At 1100°C, olivine is<br />

the liquidus phase and co-crystallized with<br />

phlogopite and augite at 1000°C for the<br />

whole range of investigated pressure and<br />

water content in the melt. At 900°C, the<br />

mineral assemblage consists of augite and<br />

phlogopite, whereas olivine is not stable.<br />

The stability field of both alkali feldspar<br />

and plagioclase is restricted to low<br />

pressure (100 MPa) and low water content<br />

(


Tracing sulfur and halogen concentrations in magmatic systems: constraints from<br />

experiments and natural glass inclusions in apatite<br />

Fleurice Parat, Francois Holtz (Universitzy Hannover), Andreas Klügel (University<br />

Bremen)<br />

Accurate methods for tracing the<br />

evolution of sulfur and halogen contents<br />

in magmatic system (pre-eruptive<br />

concentrations) are scarce and would be<br />

useful to understand the transport and/<br />

or degassing of sulfur and halogen at<br />

the scale of a volcano. Since sulfur and<br />

halogen can be incorporated in apatite at<br />

oxidizing condition, the analysis of sulfur<br />

(S), chlorine (Cl) and fluorine (F) content<br />

in apatite minerals collected from volcanic<br />

rocks is a possible indicator of volatile<br />

concentrations in melts, provided that the<br />

partitioning of volatile between apatite<br />

and melt is calibrated experimentally.<br />

Crystallization experiments have been<br />

conducted with fluid-saturated rhyolitic<br />

and andesitic melt and different bulk<br />

S contents (0.15 to 2 wt.% SO 3 ) at 900-<br />

1100°C, 400-200 MPa,XH 2 Oin =0.3-1,<br />

and ∆logƒO 2 =NNO+1-3.6. The S content<br />

in the glass increases with increasing<br />

amount of added S. The S content in apatite<br />

increases with an increase in S content in<br />

the glass. The sulfur partitioning decreases<br />

with increasing S content in glass from<br />

15.5 to 2.5 for SO 3 =0.03 to 0.28 wt.% in<br />

the glass, respectively.<br />

We found in hauyne-bearing alkaline<br />

xenoliths from La Palma (Canary Island),<br />

S-rich apatite hosted melt inclusions<br />

that represent a unique opportunity to<br />

determine direct volatile partitioning<br />

between apatite and melt and corroborate<br />

experimental studies.<br />

The determination of KdS from the<br />

analyses of glass inclusions and host<br />

34<br />

apatites in alkaline gabbros (La Palma,<br />

Canary Island) confirms the experimental<br />

results. The combination of natural and<br />

experimental data reveals that the S<br />

partition coefficient tends toward a value<br />

of 2 for high S content in the glass (>0.2<br />

wt.% SO ). Considering experimental<br />

3<br />

and natural data from this study, the S<br />

partitioning between apatite and melt can<br />

be expressed as: SO apatite = 0.157 * Ln<br />

3<br />

SO melt + 0.9834. From natural data, we<br />

3<br />

also determine the partitioning of Cl and<br />

F between apatite and melt . The partition<br />

apa/melt coefficient D ranges from 0.4 to 1.4<br />

Cl<br />

(average: 0.8). This range is consistent<br />

with results of experimental research in<br />

rhyolitic system for low Cl concentration<br />

in apatite and melt (Webster et al., 2009)<br />

and mafic silicate system (Mathez and<br />

Webster, 2005) even though the melts<br />

include different compositions.<br />

With increasing F in melt inclusions,<br />

the partition coefficients for F between<br />

apa/melt apatite and melt (D ) decrease from<br />

F<br />

40 to 3.4. We observe no correlation neither<br />

with alkalinity nor aluminosity of silicate<br />

melts. Most of our data display a high<br />

apa/<br />

partition coefficient (~40) close to DF melt determined experimentally in felsic<br />

rocks (Webster et al., 2009). This good<br />

agreement suggests that experimental<br />

results are applicable to natural system and<br />

that melt compositions has not a significant<br />

effect on sulphur and chlorine partitioning<br />

between apatite and felsic melt at waterrich<br />

and oxidized conditions.


Environmental Geosciences<br />

Influence of chemical composition, particle size and morphology on the cytotoxic<br />

and genotoxic effects of three black toner powders and their dimethylsulfoxide<br />

(DMSO) extracts in cultured human epithelial A549 lung cells in vitro<br />

Ella Goldenberg and Reto Gieré<br />

This project is part of the PhD project of Ella Goldenberg. Research collaboration<br />

with Mathias Könczöl, Volker Mersch-Sundermann and Richard Gminski (Department of<br />

Environmental Health Science, University Medical Center Freiburg, Germany), Bernard<br />

Grobéty (Department of Geosciences, University Fribourg, Switzerland) and Albrecht<br />

Seidel (Biochemisches <strong>Institut</strong> <strong>für</strong> Umweltcarcinogene, Grosshansdorf, Germany)<br />

Introduction: Toner powders for laser<br />

printers generally consist of a mixture<br />

of plastic resin, carbon black (CB) and<br />

iron oxide, often with numerous other<br />

additives such as TiO 2 and SiO 2 (Gminski<br />

et al. 2008). In humans, acute effects such<br />

as irritated eyes, headache and itching<br />

skin have been reported as being caused<br />

by exposure to toner dust. A recent study<br />

(Gminski et al., in prep.) examined<br />

selected, commercially available black<br />

toner powders as sonicated suspensions<br />

and as dimethylsulfoxide (DMSO) extracts<br />

regarding their cytotoxic (“cell damage or<br />

loss in vitality”) and genotoxic (“DNA<br />

damage”) effects in human epithelial<br />

A549 lung cells in vitro. All studied toner<br />

powder suspensions showed significant<br />

genotoxicity in the Cytochalasin Block<br />

Micronucleus (CB-MNvit) and the singlecell<br />

gel electrophoresis (COMET) assays.<br />

Furthermore, a cytotoxic effect was<br />

observed using the Lactate Dehydrogenase<br />

(LDH) assay. In our institute, we<br />

characterized the toner powders physically<br />

and chemically in order to investigate the<br />

influence of particle size, morphology and<br />

chemical composition on cytotoxicity and<br />

genotoxicity in human epithelial A549<br />

lung cells.<br />

Methods: Three black toner powders<br />

and their suspensions were examined by<br />

scanning electron microscopy (SEM)<br />

and energy-dispersive X-ray (EDX)<br />

35<br />

spectroscopy in order to determine size,<br />

shape, surface structure and elemental<br />

composition of individual toner particles.<br />

Powder X-ray Diffractometry (XRD) with<br />

Cu-Kalpha radiation was used to determine<br />

the mineral phases in the toner powders.<br />

The bulk contents of selected metals and<br />

metalloids in the toner powders were<br />

determined by graphite-furnace atomic<br />

absorption spectroscopy (AAS) (As, Pb,<br />

Sb, Ni, Cd) and flame AAS (Fe, Zn) after<br />

total digestion. The bulk Si concentration<br />

was determined using photometry.<br />

The content of polycyclic aromatic<br />

hydrocarbons (PAHs) in the toner powders<br />

was determined by gas chromatographymass<br />

spectrometry (GC-MS).<br />

Results and Discussion: The toner<br />

powders consist of C-bearing, rounded<br />

to slightly elongated particles with<br />

SEM image of toner B showing rounded<br />

submicrometer-sized magnetite particles<br />

on carbon-bearing toner particle


typical diameters of 2 to 12 μm (Figure).<br />

The particle surface is somewhat rough<br />

and is covered by rounded submicrometersized<br />

particles (0.03-0.2 μm), which are<br />

Fe- and O-rich, as shown by EDX-spectra.<br />

The toner powders are rich in Si (60000-<br />

75000 mg/kg) and Fe (30000-280000 mg/<br />

kg) and contain considerable amounts of<br />

Ni (5-23 mg/kg), Zn (31-72 mg/kg), As<br />

(22-31 mg/kg) and Pb (0.8-1.1 mg/kg).<br />

In contrast, the DMSO extracts contain<br />

hardly any metals and metalloids. The<br />

content of most PAHs varies significantly<br />

between the three toner powders. While<br />

all toner powders showed strong (dosedependent)<br />

effects in cytotoxicity, the<br />

genotoxic effects varied between the<br />

three toner powders. We conclude that<br />

the cytotoxic effects in A549 cells of the<br />

toners are probably linked to the presence<br />

36<br />

of the magnetite-covered, C-bearing<br />

particles. Moreover, we assume that the<br />

genotoxic effects may be associated with<br />

the PAHs. Which specific compounds are<br />

responsible for the toxic effects observed<br />

will be the focus of further studies.<br />

References: Gminski et al. (in prep.): Cytotoxic<br />

and genotoxic effects of three selected black toner<br />

powders and their dimethylsulfoxide (DMSO)<br />

extracts in cultured human epithelial A549 lung<br />

cells in vitro.<br />

Gminski R, Decker K, Heinz Ch, Mersch-<br />

Sundermann V (2008): Cytotoxic and genotoxic<br />

effects of three representative reprographic toner<br />

dusts and their dimethyl sulfoxide (DMSO)<br />

extracts on cultured human epithelial A 549 lung<br />

cells in vitro. N-s Arch Pharmacol, 377 (1): 82-<br />

82 (Deutsche Gesellschaft <strong>für</strong> experimentelle und<br />

klinische Pharmakologie und Toxikologie. Annual<br />

Meeting 11-13 March 2008).<br />

Risk analysis of unknown transformation products of various pharmaceuticals in<br />

the aquatic environment<br />

Marlies Bergheim, Reto Gieré, Klaus Kümmerer (<strong>Institut</strong> <strong>für</strong> Umweltmedizin und Krankenhaushygiene,<br />

Uniklinik Freiburg)<br />

Objective: The research project has<br />

started in March 2009 and its goal is to<br />

investigate and characterise the relevance,<br />

ecotoxicity and the environmental risk<br />

potential of unknown transformation<br />

products of different pharmaceuticals<br />

in the aquatic environment. The project<br />

focuses on transformation products formed<br />

by photolytic processes.<br />

Motivation: Pharmaceuticals are<br />

well-known as micropollutants in the<br />

aquatic environment. There, they are<br />

exposed to different biotic and abiotic<br />

transformation processes without being<br />

totally mineralized. In surface water, the<br />

two transformation processes hydrolysis<br />

and photodegradation play the most<br />

import role for elimination. The hereby<br />

formed transformation products and their<br />

environmental risk potential are still<br />

unknown.<br />

Methods: First, a literature research<br />

is carried out to select substances<br />

that are likely to possess an inherent<br />

environmental risk potential. High<br />

environmental input rates, biostability,<br />

solubility and photoreactivity are some<br />

of the criteria that are taken into account.<br />

To prove the stability of the substances<br />

against biotic degradation processes, the<br />

OECD standardised closed bottle test is<br />

conducted. Afterwards, the stability against<br />

photodegradation processes is tested with<br />

Hg- and Xe- lamps and is analysed by<br />

DOC monitoring. The (eco)toxicity of the<br />

hereby formed photodegradation products<br />

are further investigated with different invitro<br />

test systems. Tests on cell activity<br />

and DNA damage are performed with the<br />

WST assay and the micronucleus assay.<br />

Furthermore, the toxicity for bacteria is<br />

tested with the illumination inhibition test.


The nanoparticulate nature of invisible gold in arsenopyrite from Pezinok (Slovakia)<br />

Juraj Majzlan, Martin Chovan1, Peter Andráš2, Matthew Newville3, Michael Wiedenbeck4<br />

This research will be published: Majzlan, J., Chovan, M., Andráš, P., Newville, M.,<br />

Wiedenbeck, M., 2010: The nanoparticulate nature of invisible gold in arsenopyrite from<br />

Pezinok (Slovakia). Neues Jahrbuch <strong>für</strong> <strong>Mineralogie</strong> Abhandlungen, doi 10.1127/0077-<br />

7757/2010/0156<br />

Arsenopyrite (FeAsS) is the most<br />

common sulfide host of invisible gold.<br />

Yet, despite many studies, the position of<br />

such gold in the structure of arsenopyrite<br />

has not been resolved conclusively. We<br />

have carried out a multitechnique study<br />

of arsenopyrite samples from the Pezinok<br />

deposits (Slovakia) with moderate gold<br />

concentrations of 7-10 μg/g. Secondary<br />

ion mass spectrometry showed that gold<br />

occurs as either (1) almost uniform, lowconcentration<br />

of “dispersed” gold, or<br />

as (2) hot spots along fractures. X-ray<br />

absorption spectra at the Au L edge were<br />

collected from such hot spots (see Figure).<br />

The spectra document metallic character<br />

of gold although no discrete gold particles<br />

were seen even after careful re-examining<br />

in back-scattered electron images. We<br />

conclude that such occurrences are most<br />

readily explained by the presence of<br />

gold nanoparticles. We suggest that the<br />

dispersed gold is the chemically-bound<br />

gold previously detected in these deposits<br />

by 197Au Mössbauer spectroscopy. The<br />

concentration of this “background” gold is<br />

too low for X-ray absorption spectroscopy.<br />

normalized absorption coefficient<br />

Au(OH) 3<br />

AuCl 3<br />

AuCl<br />

AuCN<br />

Au2S Au<br />

RB243<br />

37<br />

11880 11920 11960<br />

energy (eV)<br />

X-ray absorption spectra of a number of<br />

reference compounds and the sample RB-<br />

243. The spectra of the sample show that<br />

the invisible gold in this sample is metallic<br />

gold.<br />

1 Department of Mineralogy and Petrology,<br />

Comenius University, Bratislava, Slovakia<br />

2 Department of Environmental Management,<br />

Matej Bel University, Banská Bystrica, Slovakia<br />

3 Consortium for Advanced Radiation Sources,<br />

University of Chicago, Chicago, IL USA<br />

4 Helmholtz Zentrum Potsdam, Deutsches<br />

GeoForschungsZentrum, Germany<br />

Matrix composition and community structure analysis of a novel bacterial pyrite<br />

leaching community<br />

Sibylle Ziegler1, Sonia Ackermann, Juraj Majzlan, and Johannes Gescher1<br />

These results were published as: Ziegler, S., Ackermann, S., Majzlan, J., Gescher, J.,<br />

2009: Matrix composition and community structure analysis of a novel bacterial pyrite<br />

leaching community. Environmental Microbiology 11, 2329-2338.


In collaboration with the microbiologists<br />

in Freiburg, we have studied peculiar<br />

stalactite-like objects called snottites from<br />

an underground mine in Elbingerode,<br />

Harz Mountains. Our collaborators,<br />

Sibylle Ziegler and Johannes Gescher,<br />

found these snottites and determined that<br />

these are bacterial colonies fueled by the<br />

decomposition of pyrite in this mine. The<br />

oxidation of pyrite leads to the release<br />

of ferric iron and via several steps - of<br />

sulfuric acid. This causes a dramatic<br />

decrease of the pH values which in turn<br />

leads to serious environmental problems.<br />

The novel bacterial community, described<br />

by the microbiologists, is embedded in<br />

a matrix of organic substances and bio/<br />

geochemical products of pyrite oxidation.<br />

This community grows in the snottites on<br />

the ceiling of an abandoned pyrite mine<br />

at pH values of 2.2-2.6. We measured<br />

sulfate concentrations of 200 mM and<br />

total iron concentrations of 60 mM in<br />

the soluble fraction of the matrix. Our<br />

contribution was the study of the minerals<br />

found in the snottite matrix. Micro-X-ray<br />

diffraction analysis showed that jarosite<br />

is the major mineral embedded in the<br />

biofilm matrix. X-ray absorption nearedge<br />

structure experiments at the ANKA<br />

(Karlsruhe) SUL-X beamline revealed<br />

three different sulfur species, whereby<br />

the major signal was caused by sulfate.<br />

The other two peaks might correspond to<br />

Mineralogy and Geochemistry<br />

38<br />

organic sulfur compounds. Via restriction<br />

fragment length polymorphism analysis,<br />

we elucidated the community structure.<br />

It consists mainly of iron and probably<br />

sulfur oxidizing microorganisms but also<br />

of bacteria that could be involved in the<br />

reverse reactions (dissimilatory sulfate<br />

and dissimilatory iron reducers).<br />

1 Department of Biology, Univ. Freiburg<br />

A snottite hanging from the ceiling of the<br />

old pyrite mine in Elbingerode. Photo by<br />

Sibylle Ziegler, hand of Johannes Gescher.<br />

Coal dust and the environmental impact of coal mining activities in Quang Ninh<br />

province<br />

Hoa T.B. Hoang, Reto Gieré<br />

This work is a part of the PhD project of Hoa T.B. Hoang started in October 2009.<br />

Quang Ninh province, in North-<br />

Eastern Vietnam, is one of two main coalproducing<br />

areas of Vietnam, with a total<br />

reserve of 10 billion tons. 95% of the coal<br />

used domestically and 100% of the coal<br />

exported is produced here. Vietnam Coal-


Mineral Industry Group (VINACOMIN)<br />

is the largest employer in the province<br />

and provides jobs to over 90000 workers.<br />

The coal industry is old and so are the<br />

equipment and the techniques used, which<br />

leads to considerable emissions of coal<br />

dust and wastewater, and to overburden<br />

storage.<br />

The pollution resulting from coal<br />

mining activities is a serious issue.<br />

Following the environmental 2008 report<br />

of VINACOMIN, the content of airborne<br />

dust in Quang Ninh province exceeded the<br />

Vietnamese air standards (in the period<br />

of 24 hours) by 1.2 to 5.2 times (for coal<br />

mining field) and 3.3 times (for residential<br />

areas). The water quality decreases and<br />

the marine environment is affected. The<br />

wastewater is acid, enriched in heavy<br />

metals, and its transparency is reduced due<br />

to coal dust. The health of coal mining and<br />

processing workers as well as of native<br />

people is also affected. According to the<br />

Vietnam health-disease statistics, half of<br />

the dust-induced lung diseases recorded<br />

in the country is recorded in Quang Ninh<br />

province. Typically, the lung of patients<br />

contained 2-5 mg of coal dust.<br />

39<br />

This study focuses on the mineralogical<br />

and chemical characterization of<br />

Quang Ninh coal dust and assesses the<br />

environmental impact of coal mining<br />

activities.<br />

For this study, water samples (including<br />

wastewater and seawater), coal samples,<br />

and air samples were taken in the Cam Pha<br />

area (nearly 20km 2 ), which includes the<br />

three largest open-pit coal mines of Quang<br />

Ninh and more than 10 underground coal<br />

mines. The coal and gangue samples (from<br />

both open-pit and underground mines)<br />

are being characterized mineralogically<br />

during the next year, whereas most water<br />

samples (wastewater, sea water) have<br />

already been analyzed. Particles in the air<br />

were collected with a Sigma-2 sampler in<br />

four different localities, the highest being<br />

48m above seawater level.<br />

We will also analyze the mineral<br />

content of lung lavages, i.e. of liquids<br />

obtained from rinsing the lungs of coal<br />

miners. These investigations are aimed at<br />

identifying the most important particles<br />

trapped by the lung of miners, in an effort<br />

to assess the environmental health situation<br />

in the Quang Ninh coal-mining area.<br />

Research of technology of Mn ore processing to produce high quality EMD from Toc<br />

Tat Mn ore of Vietnam<br />

Duy Anh Dao and Reto Gieré<br />

Vietnam has a great potential for<br />

mining of extensive Mn ore deposits and<br />

currently is operating 34 mines. More than<br />

10 Mt of raw Mn ore have been estimated<br />

Sigma-2 sampler on the roof of<br />

an official building at 30m above<br />

sea level near the open-pit mining<br />

area<br />

to occur in the country. Although some<br />

modern processing plants have been<br />

installed in recent years, the material<br />

produced by these plants contains only


30-35 wt% Mn, which is satisfactory<br />

for metallurgical applications only<br />

(ferromanganese materials). The material<br />

required for the production of batteries<br />

and chemicals, however, is high-purity<br />

MnO 2 (EMD, or electrolytic manganese<br />

dioxide), which thus has to be imported.<br />

The project “Research of technology of<br />

Mn ore processing to produce high quality<br />

EMD from Toc Tat Mn ore of Vietnam”<br />

was carried out in order to find a method<br />

to produce high-purity MnO 2 from<br />

Vietnamese Mn ore, so that this important<br />

material can be produced within Vietnam.<br />

The Mn ore of the Toc Tat mine as well as<br />

of the Halang Mn ore basin in northeastern<br />

Vietnam originated as neritic chemical<br />

sediment. As other rocks in the area, the<br />

ore was affected by magmatic processes<br />

and weathering after its formation. For<br />

this reason, the mineralogical composition<br />

of the studied Mn ore is very complex. The<br />

mineralogical and chemical investigation<br />

presented here reveals that the Toc Tat<br />

Mn ore contains mainly the Mn minerals<br />

pyrolusite (MnO 2 ), manganite (MnOOH),<br />

and hollandite [(K, Na, Ba) Mn 8 O 16 ]; the<br />

Fe minerals magnetite (Fe 3 O 4 ), hematite<br />

(Fe 2 O 3 ), and goethite (FeOOH); and the<br />

gangue minerals quartz (SiO 2 ) and calcite<br />

(CaCO 3 ). Additionally, small amounts of<br />

apatite (Ca 5 (PO 4 ) 3 (OH,F)) and potassium<br />

feldspar (KAlSi 3 O 8 ) may be present in<br />

some specimens. These minerals are<br />

associated with each other and commonly<br />

intergrown at a very small scale, typically<br />

on the order of several μm. These data<br />

help in determining the best strategy for<br />

the technological experiments designed to<br />

extract Mn and to transform it into highpurity<br />

MnO 2 . For example, to achieve high<br />

efficiency during the refining process, the<br />

raw ore must be ground to the size in which<br />

the Mn phases can be separated from the<br />

gangue minerals. Moreover, the best way<br />

to process the Mn ore of northeastern<br />

Vietnam is the chemical route, because the<br />

ore minerals exhibit very similar physical<br />

properties.<br />

40<br />

Leaching with SO 2 gas as a reducing<br />

agent in an H 2 SO 4 -rich solution is the<br />

suitable method for these Mn ores because<br />

the Mn minerals are present predominantly<br />

as Mn oxides. At the end of the leaching<br />

process, only 5 wt% of the Mn originally<br />

present in the raw ore remain in the residue,<br />

i.e. 95 wt% of Mn can be recovered.<br />

Moreover, less than 10 wt% of the Fe<br />

present in the raw ore was dissolved. The<br />

obtained leachate contains 71.35 g.L-1 Mn<br />

as well as several impurities, including:<br />

1870 mg.L-1 Fe; 730 mg.L-1 Al; 730<br />

mg.L-1 Ca; 810 mg.L-1 K; and small<br />

amounts of heavy metals (e.g., Cu, Cr, Co,<br />

Pb).<br />

Almost all impurities can be removed<br />

from the leachate at specific conditions.<br />

Removal of K is best achieved at the<br />

following conditions: 75-85°C, pH ~2,<br />

and addition of 40 g.L-1 jarosite seeds.<br />

Removal of Fe is best achieved at the<br />

following conditions: 20-22°C and pH<br />

~7. Conditions similar to those best suited<br />

for Fe removal were also effective in<br />

precipitating almost all the heavy metals<br />

as sulfides (by adding (NH 4 ) 2 S to the<br />

solution). The final solution, which was<br />

used for the electrolytic deposition of<br />

EMD, contains


is


Münsterbauhütte Freiburg<br />

Hiltrud Müller-Sigmund<br />

Collaboration with the Freiburg Association for Cathedral Construction continued in<br />

2009. Replacement stones for the Freiburg Münster spire were evaluated, freeze-thaw<br />

cycle tests performed and clay mineral compositions analyzed. Investigations on historical<br />

cement types were started.<br />

Thin section images of cement mortar used during restauration activities in the early 20th<br />

century (left) as opposed to historic lime mortar (right), long edges 6 mm.<br />

42


Laboratories of the MGI<br />

Public outreach activities<br />

Student field trips<br />

43


Laboratories of the MGI<br />

Gerät Analysenmöglichkeit Kontakt<br />

Tel: + 49 (0) 761 203 + ....<br />

Elektronenstrahl-Mikroanalytik Dr. H. Müller-Sigmund, Tel: 6388, 6392<br />

Elektronenstrahlmikrosonde hochgenaue automatisierte<br />

Cameca sx100, 5 Spektrometer, 14 Elementanalyse im Mikrobereich<br />

Kristalle, Elementanalyse im Mikrobereich<br />

(Elemente Be bis U), Anticon,<br />

Cl-Detektor, EDS Oxford Link ISIS<br />

• KohlenstoffbedampfungsgeräNt<br />

Edwards Auto 306,<br />

FTM7 Schichtdickenbestimmung<br />

• Au-Sputtergerät: Commonwealth<br />

Scientific Mini-Coater<br />

Röntgenanalytik I. Schmidt, Tel: 6401<br />

Röntgenfluoreszenzspektrometer qualitative und quantitative<br />

Philips 2404 mit 108-Probenwechsler chemische Materialanalyse (ab F)<br />

• Geräte zur Probenpräparation im speziellen Vollanalyse von Gesteinen<br />

(Presslinge, Schmelzlinge)<br />

Röntgenphasenanalytik I. Schmidt, Tel: 6401<br />

Röntgenpulverdiffraktometer mit Strukturanalyse von kristallinen<br />

9-fach Probenwechsler Bruker AXS D8 Festkörpern, im speziellen zur<br />

Mineralidentifikation<br />

Atomabsorptionsanalytik S. Hirth-Walther, A. Thiemann, Tel: 6397<br />

Atomabsorptionsspektrometer quantitative Elementanalyse von<br />

(AAS) Analytik Jena - Vario 6 Lösungen und Fest-stoffen<br />

Analysen im ppm-Bereich<br />

Atomabsorptionsspektrometer quantitative Elementanalyse von<br />

Perkin-Elmer 4110 ZL Zeeman Lösungen und Fest-stoffen,<br />

Analyse im ppb-Bereich<br />

Wasseranalytik S. Hirth-Walther, A. Thiemann, Tel: 6397<br />

Ionenchromatograph Dionex Anionen- und Kationen-Konzen-<br />

DX-120 mit Probensampler trationsbestimmungen (im ppm-Bereich),<br />

Photometer Perkin Elmer photometrische Konzentrations-<br />

Lambda 40 UV/VIS Bestimmung in wässrigen Lösungen<br />

Titrationsanlage Metrohm Säure/Basen, Redox- und<br />

Leitfähigkeitstitrationen<br />

Geländegeräte zur Wasseranalytik Messung von Wasserparametern<br />

(pH, Eh, Leitfähigkeit etc.) im Gelände<br />

44


Kalorimetrie Dr. Majzlan<br />

Kalorimeter CSC Isothermal Messung der Reaktionsenthalpien<br />

Microcalorimeter IMC-4400 (vorwiegend der Lösungswärme in<br />

geeigneten Lösungsmitteln) zur<br />

Bestimmung thermodynamischer<br />

Eigenschaften anorganischer Festkörper<br />

Sonstige Analytik S. Hirth-Walther, A. Thiemann, Tel: 6397<br />

Multiphasen C/H/H2O-Analysator fraktionierte Analyse von<br />

Leco RC-412 Kohlenstoff und Wasser in organischen<br />

und anorganischen<br />

Substanzen sowie auf Oberflächen<br />

C- und S-Analysator fraktionierte Analyse von<br />

Leco SC-144DR Kohlenstoff und Schwefel in organischen<br />

und anorganischen<br />

Substanzen<br />

Kammerofen Heraeus KR 170 E Erhitzen, Ausglühen von Proben<br />

bei T = 100-1150°C<br />

Aufschluss-Mikrowelle schnelle Aufschlüsse von festen<br />

MLS mPREP-A Stoffen<br />

Pyknometer Bestimmung von Dichte, Porosität und<br />

Wasseraufnahme von Mineralen und<br />

Gesteinen<br />

Mikroskopische Untersuchungen Dr. H. Müller-Sigmund, Tel: 6388, 6392<br />

Fluideinschlussmikroskop mit heiz- Bestimmung von Phasenüber<br />

und kühlbarem Probentisch Fluid Inc. gängen in Flüssigkeits- und<br />

Gaseinschlüssen in Festkörpern<br />

Kathodolumineszenzmikroskop Beobachtung des Lumineszenz-<br />

Luminoscope ELM-3 mit Photometer verhaltens von Mineralen<br />

Verschiedene Polarisationsmikroskope Identifikation und Charakterisierung von<br />

Durchlicht- und Auflicht- Mineralen im durchgehenden und<br />

untersuchungen im reflektierten Licht<br />

• Digitalkamera<br />

• Vickers-Mikrohärte<br />

• Lichtbrechungsbestimmung<br />

• Medenbach Kristallbohrgerät<br />

Gesteins- und Mineralpräparation<br />

Geräte zur Aufbereitung und D. Flemming, Tel: 6400, 8689<br />

Mineraltrennung Mineralseparation und Aufbereitung von<br />

• Frantz Magnetscheider Gesteinsproben <strong>für</strong> die Analytik<br />

• Nassschüttelherd KHD<br />

• Kugelmühle KHD<br />

• Scheibenschwingmühlen Retsch<br />

und Siebtechnik<br />

• Diverse Backenbrecher, Schüttelsiebe usw.<br />

45


• Minikern-Bohrmaschine<br />

• Sandstrahlgeräte Sandmaster FG 3-92<br />

und FG 2-94<br />

Geräte zur Präparation von Gesteinen M. Schrage, Tel: 6410<br />

Erzen und Mineralen Herstellung von Dünnschliffen<br />

• Logitech GTS1 Anschliffen und Spezialpräparaten<br />

• Logitech LP 30<br />

• Logitech LP 50<br />

• Logitech PM5<br />

• Leica DMLM mit BF, DF, IC<br />

• Div. Schleif-, Läpp- und Poliermaschinen<br />

• Eingießapparaturen<br />

Elektronenstrahlmikrosonde<br />

Dr. Hiltrud Müller-Sigmund<br />

Das wichtigste Ereignis <strong>für</strong> die Elektronenstrahlmikrosonde Cameca SX100 war in<br />

diesem Jahr die Umstellung von der 14 Jahre alten, Unix-basierten Software auf die<br />

aktuelle Software „Peak View“ unter Windows®, die im August völlig reibungslos<br />

über die Bühne ging. 2009 wurde die Mikrosonde an ca. 1100 Stunden genutzt. Davon<br />

entfielen 93 % auf institutsinterne Nutzung, 5 % auf die Studierendenausbildung und 1 %<br />

auf Fremdaufträge. Wegen Vakuum-Problemen gab es 1 Woche Ausfall.<br />

Dünnschliff Präparation<br />

Melanie Schrage<br />

Im Jahr 2009 wurden in unserem Dünnschlifflabor insgesamt 540 Proben bearbeitet.<br />

Der größte Anteil (mit ca. 79.6 %) entfällt dabei auf die Herstellung polierter und<br />

abgedeckter Dünnschliffpräparate.<br />

Ca. 11.2 % der Proben in diesem Jahr wurden von externen <strong>Institut</strong>ionen oder<br />

Privatpersonen in Auftrag gegeben.<br />

Insgesamt wurden folgende Präparate erstellt:<br />

- abgedeckte Dünnschliffe 145<br />

- polierte Dünnschliffe 285<br />

- polierte Anschliffe/Erzanschliffe 29<br />

- polierte Körnerpräparate 24<br />

- polierte Trockenschliffe 3<br />

- abgedeckte Körnerpräparate 8<br />

- polierte Dickschliffe 7<br />

- sonstige Präparationsarbeiten 39<br />

Um noch effektiver arbeiten zu können, haben wir uns dieses Jahr neben dem<br />

normalen Laborbetrieb noch intensiv mit der Verbesserung unserer Dünnschliffpolituren<br />

46


eschäftigt.<br />

Durch die Erarbeitung verschiedener neuer Methoden und durch das Ausprobieren<br />

neuer Poliermittel konnten hinsichtlich Schnelligkeit und verbesserter Gesamtpolitur<br />

gute Ergebnisse erzielt werden.<br />

Wasserlabor<br />

Sigrid Hirth-Walther/Angela Thiemann<br />

Im vergangenen Jahr wurde unser Wasserlabor von Diplomanden, Doktoranden und<br />

Bachelor während ihrer Forschungsarbeit genutzt.<br />

Einige Forschungsschwerpunkte 2009 waren :<br />

- Analytik von Oberflächenwässern aus dem Gebiet von Zermatt<br />

- Tiefenwässer aus der Alp-Transit Bohrung (NEAT)<br />

- Wässer aus der Grube Clara ( Oberwolfach )<br />

- Tracerversuche im Versuchsfeld Merdingen<br />

- Wasserproben aus Norwegen<br />

- Aufschluss- und Meßverfahren <strong>für</strong> Kohle<br />

- Wasserproben aus Vietnam<br />

Neben der Betreuung dieser Projekte, ist die Durchführung von verschiedenen<br />

Praktika, in denen den Studenten das analytische Arbeiten nahegebracht werden soll, ein<br />

großer Teil der Laborarbeit. Auch hatten wir im letzten Jahr wieder viele Aufträge aus<br />

anderen <strong>Institut</strong>en.<br />

Röntgenlabor<br />

Isolde Schmidt<br />

Im Jahr 2009 wurden im Röntgenlabor insgesamt 717 Proben präpariert und mit<br />

dem Röntgenfluoreszenspektrometer (RFA) gemessen. Im Juli diesen Jahres wurde die<br />

Software der RFA aktualisiert. Dazu wurde ein SuperQ Total Upgrade von Version 2.1 auf<br />

die neueste Version 5.0A durchgeführt.<br />

Dank unermüdlichem Einsatz unserer Frau Dr. Hiltrud Müller-Sigmund und unerwartet<br />

zur Verfügung gestellter Investitionsmittel konnte im Dezember das „Vulcan Schmelz<br />

aufschlussgerät“ in Betrieb genommen werden (siehe Fotos).<br />

47


Am Röntgendiffraktometer wurden in diesem Jahr 191 Proben untersucht.<br />

Um die Qualität unserer Analysen zu überprüfen, hat unser <strong>Institut</strong> auch in diesem Jahr<br />

an den externen Ringversuchen teilgenommen, welche von der International Association<br />

of Geoanalyst (IAG) organisiert werden. Im Rahmen dieser Ringversuche wurden die<br />

Proben Basalt HTB-1 (Basalt von Paraná Bassin) im Juni 2009 sowie die Probe OPC-<br />

1 (Ordinary Portland Cement) im Dezember 2009 analysiert. Zusätzlich beteiligten wir<br />

uns im Oktober 2009 mit umfangreichen Analysen an dem Zertifizierungsverfahren der<br />

beiden Standards OKUM (Komatiitic Basalt, Ontario) und MU-H (Harzburgite, Austria).<br />

Auch in diesem Jahr haben wir wieder zahlreichen interessierten Schülerinnen und<br />

Schülern Gelegenheit gegeben, unser Röntgenlabor zu besichtigen, z.B. im Rahmen des<br />

„Schnupperstudiums“ oder durch Einzelpraktika.<br />

Public Outreach Activites<br />

Schnupperstudium - an invitation for schoolgirls to sneak into natural sciences<br />

Hiltrud Müller-Sigmund<br />

As every year twenty schoolgirls had the opportunity to look into several aspects<br />

of studying Geosciences at the Freiburg University during 2 days in August. They got<br />

an introduction into the broad field of geosciences and witnessed a lecture on “Our<br />

Earth”. We discussed aspects of the new Bachelor of Science program, topics of study<br />

and employment prospects. Much time and personal engagement was dedicated<br />

to four workshops for hands-on experience in thin-sectioning, analyzing mineral waters,<br />

studying the application of SEM and processing of semiconductors. Lecturers, laboratory<br />

staff, and several students were involved in this well prepared and successful part of the<br />

university’s initiative to encourage girls to go for a career in geosciences.<br />

Pupils for Geosciences<br />

Hiltrud Müller-Sigmund<br />

Again, in March, we hosted a complete school class for one day to give them a deeper<br />

insight into the analysis of rocks and minerals. Pupils of the class 9 from the Hochrhein-<br />

Gymnasium Waldhut had the possibility to explore mineral formulae, different minerals,<br />

rocks and thin section microscopy. This activity forms part of the newly installed school<br />

subject “Natural Sciences and Technics”.<br />

48


Field Trips Organized by the Staff of MGI in 2009<br />

Destination Time _______ Leader<br />

Lukmanier Pass area, Switzerland 4.-5.7.2009 Bucher<br />

Finero-Baveno-Alpe Arami, Switzerland 4.-7.6.2009 Gieré<br />

Campolungo, Switzerland 11.-12.7.2009 Gieré<br />

Malenco-Bergell-Engadin, Switzerland 1.-6.9.2009 Gieré<br />

Vosges, France 20.-21.6.2009 Müller-Sigmund<br />

TREA Breisgau and MBA Kahlenberg 10.-11.7.2009 Müller-Sigmund<br />

Massif Central, France 1.-6.8.2009 Parat<br />

Aeolian Islands, Italy 31.5.-7.6.2009 Parat<br />

Finero Field Trip<br />

June 4-7, 2009<br />

Report by Philipp Sedlazeck<br />

The four Day-Field Trip was conducted by Prof. Dr. Reto Gieré and started June 14th,<br />

2009 and ended June 17th, 2009. The Field Trip’s destination was the small village Finero<br />

which is located in the North of Italy, north of the Lago Maggiore. The Field Trip’s goal<br />

was to study various magmatic and metamorphic rocks of the Alps.<br />

The first outcrop was on the top of the Gotthard Pass which was still covered in snow.<br />

The outcrop shows the Fibbia Granit. Further we went to a really beautiful place that is<br />

the destination for a lot of tourists. This place is close to the village Lavertezzo, at a river<br />

that runs down the Verzasca Valley into the Lago Maggiore. This visitor attraction is<br />

underneath a bridge which spans the river.<br />

left: Prof. Dr. Reto Gieré and students studying the outcrop; right: view from the<br />

bridge (pictures taken by Martin Voigt)<br />

49


The last outcrop for the day was in a migmatite zone and shows very well formed<br />

boudinage and several foldings. We ended the evening by having the one or other glass<br />

of wine.<br />

The second day started with an outcrop close to Finero, where we studied a beautiful<br />

Harzburgite.<br />

After a race of a few guys on the top of Mountain to the Alpe Polunia, where we<br />

made acquaintance with some goats, we looked at the next outcorp. Here harzburgite,<br />

accumulated with Chromite occurs. The next outcrops showed a garnet-rich gabbro of the<br />

lower crust, a peridotite and a mantle rock with exceptionally big amphiboles.<br />

The next day’s first stop was the quarry of the Mont’Orfano Mountain. This quarry<br />

shows a really pretty granite with a white coloured orthoclase. This quarry is the biggest<br />

and most important quarry in this region that is still beeing operated.<br />

Later, we rode to Mottarones peak, above Omegna to look at the granite that is located<br />

here. After that, we had some free time and spent it in Stresa, a little city at the Lago<br />

Maggiore and played soccer at the promenade.<br />

The last day started with an outcrop on the Passo Marco Pantani. Here is an extremly<br />

deformed, flasery gneiss to be found.<br />

Before heading back to Freiburg there was a last stop on the top of the Alpe Arami<br />

where the guys started the final race, crowned the winner and ended the field trip with the<br />

visit of the world famous garnet peridotite.<br />

This wonderful field trip to North Italy’s beautiful landscape helped to understand the<br />

observations better and made us gain a geological insight in the region around the Lago<br />

Maggiore.<br />

Field Trip Aeolian Islands<br />

May 31 – June 7, 2009<br />

Report by Dustin Marquardt<br />

A group of 17 students led by Dr. Fleurice Parat and accompanied by Ella Goldenberg<br />

went on an excursion to southern Italy. On the Aeolian Island Archipelago a series of<br />

volcanic rocks and events were looked at. Each day was reserved for one of the different<br />

islands to get an impression of island arc volcanism. On Lipari, the local expert Paola<br />

Donato joined the group and helped organize the rest of the excursion.<br />

50<br />

Group Photo on Lipari Island. In background: Vulcano Island.


The first two days were about Lipari itself. Lipari is the largest of the Aeolian Islands.<br />

The volcanic activity ranges back from at least 223 ka to recent time. The last eruption<br />

on Lipari took place in the fifth century AD when the Rocche Rosse obsidian lava flow<br />

was generated. Lipari´s volcanic history can be divided into three periods, the Pre-<br />

Tyrrhenian (223-124 ka), the Tyrrhenian (124-81 ka) and the Post-Tyrrhenian (starting<br />

81 ka) stages. Each stage has a different signature in terms of magma geochemistry and<br />

eruption style. Furthermore, each stage built up a different part of the island. Terraces of<br />

marine conglomerates on Lipari show evidence of paleo sea levels, an excellent hint on<br />

the climate of former millennia.<br />

The third day we went onto Vulcano, the southernmost volcanic island of the Aeolian<br />

Archipelago. The day started with an exhausting hike up to the crater rim. On the way<br />

up we could see active volcanic activity in form of fumaroles. Additionally, a wide view<br />

from a plateau half way up allowed us to have a look at every one of the sub aerial<br />

volcanic islands. In 183 BC, a smaller volcanic edifice, called Vulcanello, was formed<br />

north of Vulcano. Due to sedimentation the two parts were joined eventually. The last<br />

volcanic activity on Vulcano happened between 1888 and 1890.<br />

The third volcanic island to look at was Salina. A motor boat transferred us from Lipari<br />

to Salina on the fourth day, were we had a look at the oldest sub aerial volcanism of the<br />

archipelago. Amongst other things we could have a look at a dune like structure formed<br />

by pyroclastic flows. A violent plinian eruption ended volcanic activity on Salina in 13<br />

ka BC.<br />

51<br />

On the fifth day, which was probably<br />

the most exciting one, we went to<br />

Stromboli, a constantly active volcano,<br />

in fact one of the most active ones in<br />

the world. At night we had a look at the<br />

gorgeous strombolian eruptions. Every<br />

10 to 20 minutes a fountain of glowing,<br />

red lava was shot into the black sky just<br />

to land on the Sciara Del Fuoco, a large<br />

scale slide on which tons of rocks roll<br />

into the sea every hour.<br />

We used the last day to take a<br />

touristic tour through the ancient<br />

town of Pompeii. After a week of fun,<br />

good weather and with a lot of new<br />

experiences and knowledge we flew<br />

back to Germany the next morning.


Massif Central Excursion<br />

August 1–6, 2009<br />

Report by Latina Nedyalkova<br />

The focus of the excursion was the Massif Central, a volcanic region in Central France,<br />

situated between Clermont-Ferrand to the north and Montpelier to the south. Composed<br />

of several magmatic provinces, the Massif Central represents a typical example of<br />

continental intraplate alkaline volcanism. The magmatic activity in this region, which<br />

lasted from 65 Ma to 7 ka, formed variable volcanic products and landforms. During<br />

the first two days, visits of some of the Chaîne des Puys’ cinder cones and lava domes<br />

(noteworthy here are Lemptégy and Puy de Dôme) gave an insight into the formation of<br />

the chain and the structure of the volcanic edifice. The next two days put an emphasis on<br />

the strato-volcano Mont Dore, whose volcanic activity, unlike the one of Chaîne des Puys,<br />

had the characteristics of the Peléan and the Strombolian type of magmatism with higher<br />

energetic and mainly explosive eruptions. The last day of the excursion concentrated on<br />

the most eastern parts of Massif Central - the provinces Velay and Devès where the most<br />

common rock type is the basalt.<br />

The exceptional volcanism of Massif Central, formed by the interplay between<br />

lithosphere thinning and mantle upwelling due to rift-type extensional forces, provided<br />

us with an illustrative example of the diversity of magmatism and offered the rare view of<br />

perfectly formed basalt columnar joints.<br />

Group Photo on the “Puy<br />

de la Vache”<br />

52<br />

Columnar basalt at the<br />

Cheix quarry

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!