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  • 1
    Book
    Book
    Berlin : Springer
    Keywords: Metamorphic rocks ; Petrogenesis ; Metamorphose ; Metamorphes Gestein ; Lehrbuch ; Metamorphes Gestein ; Gesteinsbildung ; Metamorphes Gestein ; Metamorphose ; Gesteinskunde
    Type of Medium: Book
    Pages: XII, 428 S. , Ill., graph. Darst., Kt. , 25 cm
    Edition: 8. ed.
    ISBN: 3540741682 , 9783540741688
    DDC: 552/.4
    Language: English
    Note: Literaturangaben , pt. 1. Introduction and general aspects of metamorphism. Definition, conditions and types of metamorphism ; Metamorphic rocks ; Metamorphic processes ; Metamorphic gradept. 2. Metamorphism of specific rock types. Metamorphism of ultramafic rocks ; Metamorphism of dolomites and limestones ; Metamorphism of pelitic rocks (metapelites) ; Metamorphism of marls ; Metamorphism of mafic rocks ; Metamorphism of quartzofeldspathic rocks.
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  • 2
    Keywords: Konferenzschrift 2006 ; Geomorphologie ; Geschichte
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (336 Seiten)
    ISBN: 9781862392557
    Series Statement: Geological Society special publication 301
    DDC: 551.4109
    RVK:
    RVK:
    Language: English
    Note: Literangaben
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  • 3
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Granite. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (285 pages)
    Edition: 1st ed.
    ISBN: 9781402058912
    DDC: 552.3
    Language: English
    Note: Intro -- FM.pdf -- Ch01.pdf -- Ch02.pdf -- Ch03.pdf -- Ch04.pdf -- Ch05.pdf -- Ch06.pdf -- Ch07.pdf -- Ch08.pdf -- Ch09.pdf -- Refs.pdf -- Appendix 1.pdf -- Appendix 2.pdf -- Index.pdf.
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  • 4
    Online Resource
    Online Resource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Keywords: Metamorphism (Geology). ; Electronic books.
    Description / Table of Contents: This extensively revised and updated second edition includes the latest developments in the study of pyrometamorphism. The material covered has been derived from more than 60 new references, which are accompanied by more than 20 new illustrations.
    Type of Medium: Online Resource
    Pages: 1 online resource (369 pages)
    Edition: 2nd ed.
    ISBN: 9783642155888
    DDC: 552.4
    Language: English
    Note: Pyrometamorphism -- Preface -- Acknowledgements -- Contents -- Chapter 1 Introduction -- 1.1 Rock Terms -- 1.2 Sanidinite Facies -- Chapter 2 Thermal Regimes and Effects -- 2.1 Igneous Pyrometamorphism -- 2.1.1 Aureoles -- 2.1.2 Xenoliths -- 2.2 Combustion Pyrometamorphism -- 2.2.1 The Burning Process -- 2.2.1.1 Coal Seams -- 2.2.1.2 Carbonaceous Sediments -- 2.3 Lightning Pyrometamorphism -- 2.4 Other Thermal Effects -- 2.4.1 Columnar Jointing -- 2.4.2 Microcracking -- 2.4.3 Dilation -- 2.4.4 Preservation of Glass and Glass Compositions -- Chapter 3 Quartzofeldspathic Rocks -- 3.1 Experimental Data and Petrogenetic Grid -- 3.2 Contact Aureoles and Xenoliths -- 3.2.1 Psammitic-Pelitic Rocks and Phyllite-Schist-Gneiss Equivalents -- 3.2.1.1 South Africa -- 3.2.1.2 Apsley -- 3.2.1.3 Glenmore -- 3.2.1.4 Soay -- 3.2.1.5 Arran -- 3.2.1.6 Tieveragh -- 3.2.1.7 Mull -- 3.2.1.8 Stromboli -- 3.2.1.9 Iran -- 3.2.1.10 Auckland -- 3.2.1.11 Disco -- 3.2.1.12 Sithean Sluaigh -- 3.2.1.13 Bushveld -- 3.2.1.14 Skaergaard -- 3.2.1.15 Ngauruhoe -- 3.2.1.16 Mt. Etna -- 3.2.1.17 Traigh Bhùn na Sgùrra -- 3.2.1.18 Eifel -- 3.2.2 Sanidinite -- 3.2.2.1 Eifel -- 3.2.2.2 Mt. Amiata -- 3.2.3 Granitoids -- 3.2.3.1 Iceland -- 3.2.3.2 Sierra Nevada -- 3.2.4 Combustion Metamorphism -- 3.2.4.1 India -- 3.2.4.2 Western United States -- 3.2.4.3 Canada -- 3.2.4.4 New Zealand -- 3.2.4.5 Australia -- 3.2.4.6 Russia and Central Asia Republics -- 3.2.4.7 China -- 3.2.4.8 England -- 3.2.4.9 Mali -- 3.2.5 Lightning Strike Metamorphism -- 3.2.5.1 Winans Lake -- 3.2.5.2 Sheep Mountain -- 3.2.5.3 Hahnenstockes -- 3.2.6 Vapour Phase Crystallisation -- 3.2.6.1 Eifel -- 3.2.6.2 Vico Volcanic Complex -- Chapter 4 Calc-Silicates and Evaporates -- 4.1 Calc-Silicates -- 4.1.1 CO2 H2O in Fluid Phase -- 4.1.2 T0P0XCO2 Relations -- 4.1.2.1 Siliceous Limestone. , 4.1.2.2 Siliceous Magnesian Limestone--Dolomite -- 4.1.2.3 Marl -- 4.1.3 Contact Aureoles and Xenoliths -- 4.1.3.1 Siliceous Limestone -- 4.1.3.2 Dolomitic Limestone -- Calcitic Dolomite with Al-Fe-K -- 4.1.3.3 Siliceous Dolomite -- 4.1.4 Combustion Pyrometamorphism -- 4.1.4.1 Marly Compositions -- 4.2 Evaporites -- 4.2.1 Irkutsk -- 4.2.2 Martian Meteorite -- Chapter 5 Mafic Rocks -- 5.1 Basaltic Rocks -- 5.1.1 Contact Aureoles -- 5.1.1.1 Smartville Complex -- 5.1.1.2 Bunowen -- 5.1.1.3 Skye -- 5.1.1.4 Skaergaard -- 5.1.2 Xenoliths -- 5.1.2.1 Kap Edvard Holm Complex -- 5.1.3 Amygdules and Mesostasis -- 5.1.3.1 S Airde Beinn -- 5.1.3.2 Scawt Hill -- 5.1.4 Weathered Mafic Rocks -- 5.1.4.1 Tievbulliagh -- 5.1.4.2 Rathlin Island -- 5.1.4.3 Oregon -- 5.1.4.4 Southeastern China -- 5.1.4.5 Cameroon -- 5.2 Aluminous Ultramafic Rocks -- 5.2.1 Tari-Misaka Complex -- 5.3 Hydrothermally-Altered Andesite -- 5.3.1 White Island -- 5.4 Vapour Phase Crystallisation -- 5.4.1 Ruapehu -- 5.4.2 Vesuvius -- 5.5 Lightning Strike Fusion -- 5.5.1 Adamello -- 5.5.2 Kronotskaya Sopka -- 5.5.3 Mt. Etna -- 5.5.4 Katzenbuckel -- 5.5.5 Frankenstein -- Chapter 6 Anthropogenic and Biomass Pyrometamorphism -- 6.1 Bricks/Ceramics -- 6.1.1 Non-carbonate Mixtures -- 6.1.2 Carbonate-Bearing (Marl) Compositions -- 6.2 Spoil Heaps -- 6.2.1 Chelyabinsk -- 6.2.2 Oslavany -- 6.3 In-Situ Gasification -- 6.3.1 Centralia -- 6.3.2 Thulin -- 6.4 Contact Metamorphism of Coal and Coal Ash Fusion -- 6.4.1 Contact Metamorphism -- 6.4.2 Coal Ash Fusion -- 6.5 Biomass Surface Burning and Vitrification -- 6.5.1 Wood Ash Stones -- 6.5.2 Botswana -- 6.5.3 Tel Yin'am -- 6.5.4 Southland -- 6.5.5 Otz Valley -- 6.5.6 Vitrified Forts -- 6.5.6.1 Passo Alto -- 6.5.6.2 El Gasco -- 6.5.7 Charcoal Manufacture -- 6.5.7.1 Ricetto -- 6.5.7.2 Mt. Etna -- 6.6 Industrial Slag -- 6.6.1 Oil Shale -- 6.6.2 Blast Furnace Slag. , 6.6.3 Iron Slag -- 6.7 Inorganic Solid Waste -- 6.7.1 Wood-Fuel Ash Slag -- 6.8 Drilling -- 6.8.1 California -- 6.8.2 Denmark -- 6.9 Artificial Fulgurite -- 6.9.1 Otago -- 6.9.2 Torre de Moncorvo -- Chapter 7 Metastable Mineral Reactions -- 7.1 Quartz -- 7.2 Plagioclase -- 7.3 Muscovite -- 7.4 Chlorite -- 7.5 Biotite -- 7.6 Amphiboles -- 7.7 Clinopyroxene -- 7.8 Olivine -- 7.9 Al-Silicates -- 7.10 Garnet -- 7.11 Staurolite -- 7.12 Cordierite -- 7.13 Ankerite and Siderite -- 7.14 Pyrite and Pyrrhotite -- References -- Index.
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  • 5
    Online Resource
    Online Resource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Keywords: Metamorphism (Geology). ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (281 pages)
    Edition: 1st ed.
    ISBN: 9783540294542
    DDC: 552.4
    Language: English
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of metamorphic geology 1 (1983), S. 0 
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Abstract. Pink piemontite-spessartine-bearing and grey-green spessartine-bearing manganiferous quartzose schists derived from siliceous pelagites, and green quartzofeldspathic schists, are described from the greenschist facies of the Haast Schist terrane, near Arrow Junction, western Otago. Electron microprobe data are reported for sphene, spessartine-rich garnet, manganoan epidote, piemontite, tourmaline, phengitic muscovite, chlorite, albite, haematite, rutile, manganoan calcite and chalcopyrite.Metamorphism occurred at about 6.4kbar, 400°C. Xco2 was above the quartz-rutile-calcite-sphene buffer (Xco2± 0.02) throughout the recorded metamorphic history of the piemontite schists. It dropped from above to below this critical buffering value in a spessartine-rich schist and it was close to or below the buffering value in the quartzofeldspathic schists. Production of piemontite required high fO2, believed to be inherited from MnOx in the parent pelagite. Substantial loss of O2 (e.g. minimum of 0.19% by weight in one rock) during diagenesis and/or metamorphism is inferred. In the grey-green schists this inhibited piemontite formation. Slight loss of O2 and Ca2+ accompanied minor late-stage replacement of piemontite by second generation spessartine. Observed zoning and mineral replacements indicate rise of temperature, drop in pressure, or invasion by solutions of lower fO2 and XCO2 equilibrated with surrounding schists.The detailed chemistry of the minerals studied correlates with available Mn and with bulk-rock (Fe3+ x 100)/(Fe2++ Fe3+). The oxidation ratio ranges from 24 in average green quartzofeldspathic schist, through 78 in average grey-green manganiferous quartzose schist, to almost 100 in some piemontite-bearing schists. As Fe2+ gives way to Fe3+, Mg/Fe ratios tend to rise in chlorite, phengite, tourmaline, spessartine, and calcite, Mn increases and Ti decreases in haematite, Mn increases in spessartine and calcite, and Fe increases in rutile. Available divalent cations are depleted relative to Al; chlorite is more aluminous, and phengite more paragonitic than in typical Haast schists.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of metamorphic geology 1 (1983), S. 0 
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Plagioclase compositions vary from An0.1–2.5 to An32 with increasing grade in chlorite zone to oligoclase zone quartzofeldspathic schists, Franz Josef-Fox Glacier area, Southern Alps, New Zealand. This change is interrupted by the peristerite composition gap in rocks transitional between greenschist and amphibolite facies grade. Oligoclase (An20-24) and albite (An0.1–0.5) are found in biotite zone schists below the garnet isograd. With increasing grade, the plagioclase compositions outline the peristerite gap, which is asymmetric and narrows to compositions of An12 and An6 near the top of the garnet zone. In any one sample, oligoclase is the stable mineral in mica-rich layers above the garnet isograd, whereas albite and oligoclase exist in apparent textural equilibrium in adjacent quartz-plagioclase layers. The initial appearance of oligoclase in both layers results from the breakdown of epidote and possibly sphene. Carbonate is restricted to the quartz-plagioclase rich layers and probably accounts for the more sodic composition of oligoclase in these layers. The formation of more Ca-rich albite and more Na-rich oligoclase near the upper limit of the garnet zone coincides with the disappearance of carbonate and closure of the peristerite gap. Garnet appears to have only a localized effect on Ca-enrichment of plagioclase in mica-rich layers within the garnet zone. The Na-content of white mica increases sympathetically with increasing Ca-content of oligoclase and metamorphic grade.Comparison of the peristerite gap in the Franz Josef-Fox Glacier schists and schists of the same bulk composition in the Haast River area, 80 km to the S, indicates that oligoclase appears and epidote disappears at lower temperatures, and that the composition gap between coexisting albite and oligoclase is narrower in the Franz Josef-Fox Glacier area. It is suggested that a higher thermal gradient (38-40°C/km) and variations in Si/Al ordering during growth of the plagioclases between the two areas may account for these differences. In the Alpine schists the peristerite gap exists over a temperature and pressure interval of about 370-515°C and 5.5-7 kbar (550-700 MPa) PH2O.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 68 (1978), S. 23-35 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Manganiferous quartz-mica schists (4 m in stratigraphic thickness) overlie epidote amphibolite in the Chiroro River area, Hidaka Mountains, Hokkaido. The schist layers have a considerable range of A/F ratios and bulk oxidation ratios which vary from 21.5 to 100. Manganese contents are from 4 to 30 times higher than that of the average shale with 0.09% MnO. The schists are essentially quartz-white mica-biotite-Mn garnet-tourmaline-±epidote-magnetite assemblages. A highly oxidized layer (5–8 cm thick) 95 cm above the epidote amphibolite contact is characterized by viridine-piemontite-spessartine-Mn white mica-Mn tourmaline-Ti-Mn haematite indicative of both high initial manganese content and very high f O2 conditions of recrystallization. Viridine contains up to 17 mol% Mn3+SiO5 and coexists with piemontite with between 13.6 and 15.4 wt% Mn2O3. Mn-poor-Fe-rich (Ps32) epidote occurs in the less oxidized schist enclosing the viridine-piemontite bearing seam. Garnets vary widely in composition with end member variations (mol%) of Spess22.9–80.5; And0.2–11.7; Alm1.1–57.1; Pyr2.0–12.2; Gross7.0–49.0. The more manganiferous garnets occur in rocks with higher oxidation ratios while almandiferous varieties occur in schists with low oxidation ratios. Biotite ranges from green to red-brown varieties (increasing Ti and Fe) with Mg/ (Mg+Fe) ratios varying from 56 to 48. Ten to fifteen percent octahedral R2+ is replaced by Al indicating a trend towards eastonite-siderophyllite. The white micas deviate only slightly from dioctahedral stoichiometry but have up to 25% of octahedral sites occupied by Fe, Mg and to a lesser extent Mn and Ti as R2+ Si4+⇌2Al3+ and in highly oxidized rocks as (Fe,Mn)3+⇌Al3+. The white mica in the highly oxidized viridine-piemontite schist is pale pinkishorange, exhibits reverse pleochroism, and has between 0.30 and 0.43 wt% Mn2O3. There is a close comparison, both in terms of stratigraphic thickness and Fe-Mn variation, between the Chiroro schist sequence and many oceanic cores so that the bulk chemistry and mineralogy of the pelitic schists is largely an extension of the original Eh-pH conditions of hemipelagic sedimentation and post-depositional adjustments during diagenesis. The thin viridine-piemontite bearing schist is correlated with an oxidized, Fe-Mn rich layer commonly found in present day oceanic cores. The viridine presumably formed by reaction of original ferro-manganese microgranules and clay minerals. Halmrolytic alteration of the underlying metabasalt resulted in leaching of Mn and Fe (in particular) into the overlying sediments and the formation of concentrations of haematite — manganese oxide — Mn garnet along the schist-epidote amphibolite contact. Estimation of the P-T conditions of metamorphism from the phase relations and compositions in the epidote amphibolite associated with the manganiferous schist gives T °C = 530∼560 and a minimum P fluid 〉 3 kb which corresponds to the epidote amphibolite facies of Barrovian-type terrains.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 49 (1975), S. 125-140 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Actinolite-actinolitic hornblende and actinolitic hornblende-hornblende pairs are described from gabbroic amphibolites and epidote amphibolites formed by dynamic metamorphism during uplift of gabbroic rooks in the Hidaka Metamorphic Belt, Hokkaido. Electron microprobe analyses indicate that coupled substitutions involved in the transition from actinolite to hornblende are essentially those of edenite and tschermakite-ferritschermakite together with smaller amounts of glaucophane-riebeckite, i.e. AlIV, AlVI, Fe3+, A-site occupancy and NaM4 increase with replacement of Mg by Fe2++ Mn and Si by AlIV. During metamorphism the amount of deformation due to shearing has affected the degree of compositional discontinuity in the actinolite-hornblende series and the compositional gap is most pronounced in the epidote amphibolite. The coexisting actinolite-hornblende do not represent an equilibrium pair as textural relations indicate that the actinolitic amphiboles are relics. It is suggested that shearing deformation during uplift has caused an overstepping of the changing physico-chemical conditions of metamorphism so that compositional readjustment of amphiboles was not achieved. Equilibrium-disequilibrium actinolite-hornblende pairs are discussed from other localities where rocks of basaltic composition have been metamorphosed.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 69 (1979), S. 97-103 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Aenigmatite, sodic pyroxene and arfvedsonite occur as interstitial minerals in metaluminous to weakly peralkaline syenite patches in alkali dolerite, Morotu, Sakhalin. Aenigmatite is zoned from Ca, Al, Fe3+-rich cores to Ti, Na, Mn, Si-rich rims reflecting the main substitutions Fe2+Ti4+⇌Fe3+, NaSi⇌CaAl and Mn2+⇌Fe2+. Aenigmatite replaces aegirine and ilmenite supporting the existence of a ‘no-oxide’ field in $$f_{{\text{O}}_{\text{2}} }$$ — T space. In one case aenigmatite has apparently formed by reaction between ilmenite and arfvedsonite. Titanian aegirine (up to 3.0 wt% TiO2) and Fe-chlorite may replace aenigmatite. Sodic pyroxene occurs as zoned crystals with cores of aegirine-augite rimmed by aegirine and in turn by pale green aegirine containing 93 mol% NaFe3+Si2O6. Additional substitution of the type NaAl⇌CaFe2+ is indicated by significant amounts (up to 6 mol%) of NaAlSi2O6. Arfvedsonite is zoned with rims enriched in Na, Fe and depleted in Ca which parallels the variation of these elements in the sodic pyroxenes. The high peralkalinity of the residual liquid from which the mafic phases formed resulted from the early crystallization of microperthite (which makes up the bulk of the syenites) leading to an increase in the Na2O/(Na2O+K2O) and (Na2O+K2O)/Al2O3 ratios of the remaining interstitial liquid which is also enriched in Ti, Fe, and Mn. Bulk composition of the melt, $$f_{{\text{O}}_{\text{2}} }$$ , temperature and volatile content were all important variables in determining the composition and stability of the peralkaline silicates. $$f_{{\text{O}}_{\text{2}} }$$ in the residual liquid appears to have been buffered by arfvedsonite-aegirine and later by the arfvedsonite-aenigmatite and aenigmatite-aegirine equilibria under $$f_{{\text{O}}_{\text{2}} }$$ conditions of a ‘no-oxide’ field. An increase in $$f_{{\text{O}}_{\text{2}} }$$ , above that of the alkali buffer reactions, is inferred by an increase of Ti and Mn in aenigmatite rims. The latest postmagmatic vapour crystallization stage of the syenites is marked by extremely low $$f_{{\text{O}}_{\text{2}} }$$ which may have been facilitated by exsolution of a gas phase. Low $$f_{{\text{O}}_{\text{2}} }$$ is supported by the replacement of aenigmatite by titanian aegirine, and the formation of rare Ti-rich garnet with a very low (ΣTi4++Fe3+)/(ΣTi+ΣFe) ratio of 0.51, associated with leucoxene alteration of ilmenite.
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