Initiation and Evolution of Subduction: T-T-D History of the Easton Metamorphic Suite, Northwest Washington State
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Washington State Minerals Checklist
Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite -
Yellowish Green Diopside and Tremolite from Merelani, Tanzania
YELLOWISH GREEN DIOPSIDE AND TREMOLITE FROM MERELANI, TANZANIA Eric A. Fritz, Brendan M. Laurs, Robert T. Downs, and Gelu Costin tion (typical of diopside, which is a pyroxene) shown by other crystals in the parcels. Four similar-appearing yellowish green samples Mr. Ulatowski loaned one example of both types of from Block D at Merelani, Tanzania, were identified crystals to GIA for examination (figure 1), and we also as diopside and tremolite. The gems are identical in color, but their standard gemological properties are typical for calcic pyroxene and amphibole. The identification of the diopside was made with Raman Figure 1. These yellowish green crystals were recov- spectroscopy, while single-crystal X-ray diffraction ered from Block D at Merelani in the latter part of and electron-microprobe analyses were used to 2005. A blocky morphology is shown by the diopside confirm the amphibole species as tremolite. crystal (1.6 cm tall; left and bottom), whereas the Absorption spectroscopy (in the visible–mid-infrared tremolite crystal has a flattened, diamond-shaped range) revealed that the two gem materials are col- cross-section. Photos by Robert Weldon. ored by V3+, Cr3+, or both. t the 2006 Tucson gem shows, Steve Ulatowski A showed one of the authors (BML) some yellowish green crystals that he purchased as diopside while on buy- ing trips to Tanzania in August and November 2005. The material was reportedly produced during this time period from Block D at Merelani, in the same area that yielded some large tsavorite gem rough (see Laurs, 2006). Mr. Ula- towski obtained 1,200 grams of the green crystals, mostly as broken pieces ranging from 0.1 to 50 g (typically 1–5 g). -
The Structure of Stilpnomelane Reexamined
THE STRUCTURE OF STILPNOMELANE REEXAMINED JouN W. Gnunon, Uniaersity of Minnesota, Mi.nneapolis,Minnesota. Assrnect New r-ray data show the distribution of ions normal to the basal cleavage in the layer silicate stilpnomelane. Since it is similarto talc and biotite a structure consistentwithits properties can be proposed. It explains satisfactorily the behavior of the mineral including its base exchange of K for Tl. Stilpnomelane is an important essential constituent of certain iron formations. fNrnooucrroN The writer (1) made an attempt in 1937 to determine the composition and crystal structure of stilpnomelane. At that time the mineral had been reported from the quartz veins in iron formations and from the chlorite-epidote-albite schists in New Zealand (8 and 11). Recently it has been identified in large amounts in the iron formations of the Cuyuna and Mesabi ranges of Minnesota. There it is one of the three principal iron silicates,iron talc, to be describedin detail shortly, being the second and greenalite the third. As was pointed out previously, (1, p. 912) stilpnomelane may readily be mistaken for biotite under the microscope.Like biotite it is negative with a small optic angle and has similar pleochroism. In the hand speci- men it resembleseither biotite or chlorite, but is much more brittle. Its cleavageis excellent. Basal sections with partially developed hexagonal outlines have been observed. These properties and the discussion that follows make it certain that stilpnomelane has a layer structure and is related to the micas and chlorites. CnBurcar CouposrrroN Nothing essentially new can be added with regard to the chemical composition of stilpnomelane. -
Facies and Mafic
Metamorphic Facies and Metamorphosed Mafic Rocks l V.M. Goldschmidt (1911, 1912a), contact Metamorphic Facies and metamorphosed pelitic, calcareous, and Metamorphosed Mafic Rocks psammitic hornfelses in the Oslo region l Relatively simple mineral assemblages Reading: Winter Chapter 25. (< 6 major minerals) in the inner zones of the aureoles around granitoid intrusives l Equilibrium mineral assemblage related to Xbulk Metamorphic Facies Metamorphic Facies l Pentii Eskola (1914, 1915) Orijärvi, S. l Certain mineral pairs (e.g. anorthite + hypersthene) Finland were consistently present in rocks of appropriate l Rocks with K-feldspar + cordierite at Oslo composition, whereas the compositionally contained the compositionally equivalent pair equivalent pair (diopside + andalusite) was not biotite + muscovite at Orijärvi l If two alternative assemblages are X-equivalent, l Eskola: difference must reflect differing we must be able to relate them by a reaction physical conditions l In this case the reaction is simple: l Finnish rocks (more hydrous and lower MgSiO3 + CaAl2Si2O8 = CaMgSi2O6 + Al2SiO5 volume assemblage) equilibrated at lower En An Di Als temperatures and higher pressures than the Norwegian ones Metamorphic Facies Metamorphic Facies Oslo: Ksp + Cord l Eskola (1915) developed the concept of Orijärvi: Bi + Mu metamorphic facies: Reaction: “In any rock or metamorphic formation which has 2 KMg3AlSi 3O10(OH)2 + 6 KAl2AlSi 3O10(OH)2 + 15 SiO2 arrived at a chemical equilibrium through Bt Ms Qtz metamorphism at constant temperature and = -
X-Ray Structure Refinements of Tremolite at 140 and 295 K: Crystal Chemistry and Petrologic Implications
American Mineralogist, Volume 81, pages 1117-1125,1996 X-ray structure refinements of tremolite at 140 and 295 K: Crystal chemistry and petrologic implications HEXIONG YANG1.. ANDBERNARD W. EVANS2 'Department of Geological Sciences. Campus Box 250, University of Colorado, Boulder, Colorado 80309-0250, U.S.A. 2Department of Geological Sciences, Box 351310, University of Washington, Seattle, Washington 98195-1310, U.S.A. ABSTRACT A near-end-member natural tremolite, N!lo.o,Ca1.97M~.9sFeo.Q3Alo.oISis.oo022(OH)2'was studied by single-crystal X-ray diffraction at 140 and 295 K to seek a possible crystal- chemical explanation for the typically low CaI~ M ratios, relative to the ideal ratio of 2/5, observed in both natural and synthetic tremolite samples. Difference-Fourier maps re- vealed the presence of a residual electron density close to the M4 site along the diad axis toward the octahedral strip. Structure refinements indicated that the M4 and M4' sites are occupied by Ca + Na and M(Fe + Mg), respectively. In comparison with the configuration of the M2 coordination polyhedron in diopside, the degree of distortion and the volume of the M4 coordination polyhedron in tremolite are relatively large and the M4 cation is slightly underbonded. These two factors contribute to an energetic drive toward M-en- riched tremolite. The average unit-cell volume of 906.6(2) A3 determined at 295 K for nearly pure tremolite in this study suggests an end-member reference-state volume for tremolite of907 A3. This indicates that cell volumes of synthetic tremolite of 904.2(4) A3 reflect 8-10% cummingtonite solid solution, as previous authors have claimed. -
Finding of Prehnite-Pumpellyite Facies Metabasites from the Kurosegawa Belt in Yatsushiro Area, Kyushu, Japan
Journal ofPrehnite Mineralogical-pumpellyite and Petrological facies metabasites Sciences, in Yatsushiro Volume 107, area, page Kyushu 99─ 104, 2012 99 LETTER Finding of prehnite-pumpellyite facies metabasites from the Kurosegawa belt in Yatsushiro area, Kyushu, Japan * * ** Kenichiro KAMIMURA , Takao HIRAJIMA and Yoshiyuki FUJIMOTO *Department of Geology and Mineralogy, Graduate School of Science, Kyoto University, Kitashirakawa Oiwakecho, Kyoto 606-8502, Japan ** Nittetsu-Kogyo Co., Ltd, 2-3-2 Marunouchi, Chiyoda, Tokyo 100-8377, Japan. Common occurrence of prehnite and pumpellyite is newly identified from metabasites of Tobiishi sub-unit in the Kurosegawa belt, Yatsushiro area, Kyushu, where Ueta (1961) had mapped as a greenschist facies area. Prehnite and pumpellyite are closely associated with chlorite, calcite and quartz, and they mainly occur in white colored veins or in amygdules in metabasites of the relevant area, but actinolite and epidote are rare in them. Pumpellyite is characterized by iron-rich composition (7.2-20.0 wt% as total iron as FeO) and its range almost overlaps with those in prehnite-pumpellyite facies metabasites of Ishizuka (1991). These facts suggest that the metabasites of the Tobiishi sub-unit suffered the prehnite-pumpellyite facies metamorphism, instead of the greenschist facies. Keywords: Prehnite-pumpellyite facies, Lawsonite-blueschist facies, Kurosegawa belt INTRODUCTION 1961; Kato et al., 1984; Maruyama et al., 1984; Tsujimori and Itaya, 1999; Tomiyoshi and Takasu, 2009). Until now, The subduction zone has an essential role for the global there is neither clear geological nor petrological evidence circulation of solid, fluid and volatile materials between suggesting what type of metamorphic rocks occupied the the surface and inside of the Earth at present. -
Approaches to the Low Grade Metamorphic History of the Karakaya Complex by Chlorite Mineralogy and Geochemistry
Minerals 2015, 5, 221-246; doi:10.3390/min5020221 OPEN ACCESS minerals ISSN 2075-163X www.mdpi.com/journal/minerals Article Approaches to the Low Grade Metamorphic History of the Karakaya Complex by Chlorite Mineralogy and Geochemistry Sema Tetiker 1, Hüseyin Yalçın 2,* and Ömer Bozkaya 3 1 Department of Geological Engineering, Batman University, 72100 Batman, Turkey; E-Mail: [email protected] 2 Department of Geological Engineering, Cumhuriyet University, 58140 Sivas, Turkey 3 Department of Geological Engineering, Pamukkale University, 20070 Denizli, Turkey; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +90-0542-412-16-19. Academic Editor: Antonio Simonetti Received: 18 November 2014 / Accepted: 9 April 2015 / Published: 16 April 2015 Abstract: In this study, chlorite is used to investigate the diagenetic-metamorphic evolution and accurate geological history of the different units belonging to the Karakaya complex, Turkey. Primary and secondary chlorite minerals in the very low-grade metamorphic rocks display interference colors of blue and brown and an appearance of optical isotropy. Chlorites are present in the matrix, pores, and/or rocks units as platy/flaky and partly radial forms. X-ray diffraction (XRD) data indicate that Mg-Fe chlorites with entirely IIb polytype (trioctahedral) exhibit a variety of compositions, such as brunsvigite-diabantite-chamosite. The major element contents and structural formulas of chlorite also suggest these were derived from both felsic and metabasic source rocks. Trace and rare earth element (REE) concentrations of chlorites increase with increasing grade of metamorphism, and these geochemical changes can be related to the tectonic structures, formational mechanics, and environments present during their generation. -
Hydrogen-Bonded Water in Laumontite I: X-Ray Powder Diffraction Study Of
American Mineralogist, Volume 88, pages 277–287, 2003 Hydrogen-bonded water in laumontite I: X-ray powder diffraction study of water site occupancy and structural changes in laumontite during room-temperature isothermal hydration/dehydration THRÁINN FRIDRIKSSON,1,* DAVID L. BISH,2 AND DENNIS K. BIRD1 1Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305-2115, U.S.A. 2Hydrology, Geochemistry, and Geology, MS D469, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, U.S.A. ABSTRACT The response of the laumontite crystal structure to hydration/dehydration was evaluated using Rietveld refinements with XRD data collected under controlled PH2O conditions at ~28.5 ∞C. Refined water contents per unit cell (unit-cell formula: Ca4Al8Si16O48·nH2O) ranged between 12.5 H2O at 0.11 mbar PH2O and 17.3 H2O at 37.6 mbar. The occupancy of the two water sites hosting hydrogen- bonded water molecules, W5 and W1, ranged from 13% to 100% and from 2% to 86%, respectively. During hydration of W5, between 0.11 and 5 mbar, the unit cell expanded continuously and revers- ibly from 1327 to 1348 Å3. The unit-cell volume remained nearly constant between 5 and 28 mbar. The hydration/dehydration of W1 exhibited hysteresis; hydration occurred at ~29 mbar and dehy- dration at ~24 mbar. During hydration of W1 at ~29 mbar the unit cell expanded from 1351 to 1384 Å3. Further hydration of W1 above 29 mbar resulted in gradual and reversible unit-cell expansion to 1386 Å3 at 37.6 mbar. Hydration/dehydration of W5 is a continuous reaction typical for zeolites. -
List of Abbreviations
List of Abbreviations Ab albite Cbz chabazite Fa fayalite Acm acmite Cc chalcocite Fac ferroactinolite Act actinolite Ccl chrysocolla Fcp ferrocarpholite Adr andradite Ccn cancrinite Fed ferroedenite Agt aegirine-augite Ccp chalcopyrite Flt fluorite Ak akermanite Cel celadonite Fo forsterite Alm almandine Cen clinoenstatite Fpa ferropargasite Aln allanite Cfs clinoferrosilite Fs ferrosilite ( ortho) Als aluminosilicate Chl chlorite Fst fassite Am amphibole Chn chondrodite Fts ferrotscher- An anorthite Chr chromite makite And andalusite Chu clinohumite Gbs gibbsite Anh anhydrite Cld chloritoid Ged gedrite Ank ankerite Cls celestite Gh gehlenite Anl analcite Cp carpholite Gln glaucophane Ann annite Cpx Ca clinopyroxene Glt glauconite Ant anatase Crd cordierite Gn galena Ap apatite ern carnegieite Gp gypsum Apo apophyllite Crn corundum Gr graphite Apy arsenopyrite Crs cristroballite Grs grossular Arf arfvedsonite Cs coesite Grt garnet Arg aragonite Cst cassiterite Gru grunerite Atg antigorite Ctl chrysotile Gt goethite Ath anthophyllite Cum cummingtonite Hbl hornblende Aug augite Cv covellite He hercynite Ax axinite Czo clinozoisite Hd hedenbergite Bhm boehmite Dg diginite Hem hematite Bn bornite Di diopside Hl halite Brc brucite Dia diamond Hs hastingsite Brk brookite Dol dolomite Hu humite Brl beryl Drv dravite Hul heulandite Brt barite Dsp diaspore Hyn haiiyne Bst bustamite Eck eckermannite Ill illite Bt biotite Ed edenite Ilm ilmenite Cal calcite Elb elbaite Jd jadeite Cam Ca clinoamphi- En enstatite ( ortho) Jh johannsenite bole Ep epidote -
What We Know About Subduction Zones from the Metamorphic Rock Record
What we know about subduction zones from the metamorphic rock record Sarah Penniston-Dorland University of Maryland Subduction zones are complex We can learn a lot about processes occurring within active subduction zones by analysis of metamorphic rocks exhumed from ancient subduction zones Accreonary prism • Rocks are exhumed from a wide range of different parts of subduction zones. • Exhumed rocks from fossil subduction zones tell us about materials, conditions and processes within subduction zones • They provide complementary information to observations from active subduction systems Tatsumi, 2005 The subduction interface is more complex than we usually draw Mélange (Bebout, and Penniston-Dorland, 2015) Information from exhumed metamorphic rocks 1. Thermal structure The minerals in exhumed rocks of the subducted slab provide information about the thermal structure of subduction zones. 2. Fluids Metamorphism generates fluids. Fossil subduction zones preserve records of fluid-related processes. 3. Rheology and deformation Rocks from fossil subduction zones record deformation histories and provide information about the nature of the interface and the physical properties of rocks at the interface. 4. Geochemical cycling Metamorphism of the subducting slab plays a key role in the cycling of various elements through subduction zones. Thermal structure Equilibrium Thermodynamics provides the basis for estimating P-T conditions using mineral assemblages and compositions Systems act to minimize Gibbs Free Energy (chemical potential energy) Metamorphic facies and tectonic environment SubduconSubducon zone metamorphism zone metamorphism Regional metamorphism during collision Mid-ocean ridge metamorphism Contact metamorphism around plutons Determining P-T conditions from metamorphic rocks Assumption of chemical equilibrium Classic thermobarometry Based on equilibrium reactions for minerals in rocks, uses the compositions of those minerals and their thermodynamic properties e.g. -
The Greenschist to Amphibolite Facies Tonalite-Greenstone Terrain of The
95 THE PIKWITONEI GRANULITE DOMAIN: A LOWER CRUSTAL LEVEL ALONG THE CHURCHILL-SUPERIOR BOUNDARY IN CENTRAL MANITOBA. W. Weber, Manitoba Geological Services Branch, Winnipeg, Manitoba, Canada, R3H OW4 The greenschist to amphibolite facies tonalite-greenstone terrain of the Gods Lake subprovince grades - in a northwesterly direction - into the granulite facies Pikwitonei domain (1) at the western margins of the Superior Province,. The transition is the result of prograde metamorphism and takes place over 50 - 100 km without any structural or lithological breaks. Locally the orthopyroxene isograd is oblique to the structural grain and transects greenstone belts, e.g., the Cross Lake belt (2). The greenstone belts in the granulite facies and adjacent lower grade domain consist mainly of mafic and (minor) ultramafic metavolcanics, and clastic and chemical metasedimentary rocks (1,2). Typical for the greenstone belts crossed by the orthopyroxene isograd are anorthositic gabbros and anorthosites, and plagiophyric mafic flows. Available data suggest a late Aphebian age for the prograde greenschist to granulite facies metamorphism. Peak conditions are reflected by saphirin-bearing and opx-sillimanite quartz gneisses which indicate 10 - 11 kb pressure and temperatures of 900 - 1000°C (2). At its western and northern edge - towards the contact with the Churchill Province - the rocks of the Pikwitonei granulite domain were overprinted by the Hudsonian orogeny; they were deformed, selectively retrogressed and recrystallized under greenschist to amphibolite facies conditions (1,2); locally they were migmatized. The Thompson belt, the Split Lake block and a linear zone south of the Fox River consists of these reworked granulites. Proterozoic rocks of the Circum-Superior belt (3) (apparently) overlie the reworked granulites along the Fox River and in the Thompson belt. -
Tungsten Minerals and Deposits
DEPARTMENT OF THE INTERIOR FRANKLIN K. LANE, Secretary UNITED STATES GEOLOGICAL SURVEY GEORGE OTIS SMITH, Director Bulletin 652 4"^ TUNGSTEN MINERALS AND DEPOSITS BY FRANK L. HESS WASHINGTON GOVERNMENT PRINTING OFFICE 1917 ADDITIONAL COPIES OF THIS PUBLICATION MAY BE PROCURED FROM THE SUPERINTENDENT OF DOCUMENTS GOVERNMENT PRINTING OFFICE WASHINGTON, D. C. AT 25 CENTS PER COPY CONTENTS. Page. Introduction.............................................................. , 7 Inquiries concerning tungsten......................................... 7 Survey publications on tungsten........................................ 7 Scope of this report.................................................... 9 Technical terms...................................................... 9 Tungsten................................................................. H Characteristics and properties........................................... n Uses................................................................. 15 Forms in which tungsten is found...................................... 18 Tungsten minerals........................................................ 19 Chemical and physical features......................................... 19 The wolframites...................................................... 21 Composition...................................................... 21 Ferberite......................................................... 22 Physical features.............................................. 22 Minerals of similar appearance.................................