Texturally-early fluid inclusions in garnets: evidence of the prograde metamorphic path?

Well-formed, texturally-early fluid inclusions in garnets from the Archean Pikwitonei granulite domain, Manitoba, Canada, have been analyzed using microthermometric methods. The mean CO₂ homogenization temperature (to liquid) for inclusions in 12 of 13 samples from the Cauchon Lake-Nelson River area is +15.2° C (n=125, 2σ=8.2° C), corresponding to a CO₂ density of 0.82 g/cm³. Inclusions in the remaining sample have somewhat lower CO₂ homogenization temperatures (mean=+5.4° C, n=24). The studied inclusions contain an estimated 10 to 20 vol. percent H₂O, with minor amounts of other fluid species such as CH₄, N₂, and/or H₂S. The fluid inclusions were probably trapped during early garnet growth at relatively low pressures (≤5 kbar if at 750° C), and appear to have undergone only limited or possibly no subsequent re-equilibration. This interpretation is consistent with the “anti-clock-wise” P-T-t path (heating before loading) determined for the Pikwitonei region by other workers. For such a prograde path, inclusions entrapped early, at high temperatures but at relatively low pressures, would experience internal underpressures during most of the subsequent prograde and retrograde phases of metamorphism. The texturally-early fluid inclusions in garnets from the Pikwitonei region therefore cannot be used to provide direct information about the highest metamorphic temperature and pressure conditions (750° C and 7 kbar). However, the results obtained in this study suggest that texturally-early fluid inclusions in garnets may, in some cases, retain evidence of the prograde metamorphic path.     

Metamorphic <Emphasis Type="Italic">P</Emphasis>–<Emphasis Type="Italic">T</Emphasis> paths of the Zanhuang amphibolites and metapelites: constraints on the tectonic evolution of the Paleoproterozoic Trans-North China Orogen

Garnet-bearing metapelites and amphibolites are exposed in the south and middle parts of the Zanhuang complex, which is located in the central segment of the nearly NS-striking Trans-North China Orogen. These rocks preserve three metamorphic mineral assemblages forming at the prograde, peak and post-peak decompression stages. The prograde metamorphic stage (M₁) is represented by mineral inclusions within garnet porphyroblasts, the peak metamorphic stage (M₂) is represented by garnet rims and matrix minerals, whereas the retrograde stage (M₃) is represented by amphibole + plagioclase symplectite rimming garnet porphyroblasts in the amphibolites and biotite + plagioclase symplectite rimming garnet porphyroblasts in the metapelites. All garnet porphyroblasts in the metapelites preserve prograde chemical zoning except for the ubiquitous, quite narrow zones from the underwent post-peak decompression. It has been determined through thermobarometric computation that the metamorphic conditions are 650–710°C at 8.2−9.2 kbar for the M₁ (inclusion) assemblages, >810°C at >12.5 kbar for the metamorphic peak M₂ (matrix) assemblages, and 660–680°C at 4.4–4.5 kbar for the retrograde M₃ (symplectite) assemblages. These rocks are thus determined to have undergone metamorphism with clockwise P–T paths involving nearly isothermal decompression (ITD) segments, which is inferred to be related to the amalgamation of the Eastern and Western Blocks to form the coherent basement of the North China Craton along the Trans-North China Orogen in the late Paleoproterozoic (1.88–1.85 Ga).     

Kornerupine parageneses in whiteschists and other magnesian rocks: is kornerupine + talc a high-pressure assemblage equivalent to tourmaline + orthoamphibole?

Kornerupine, (□,Fe,Mg)(Mg,Fe,Al)₉(Si,Al,B)₅ (O,OH,F)₂₂, has been reported with talc in rocks from six localities worldwide, but only at Chilapila Hill in the Lufilian Arc, Zambia do textural relationships imply that kornerupine (Krn) equilibrated with talc (Tlc) during a prograde metamorphic event at T≈ 640 °C, P≈ 13 kbar; a prograde Krn + Tlc assemblage has also been reported from Mautia Hill, Tanzania (P ≤ 13 kbar). In order to estimate possible constraints on the stability range for the kornerupine + talc paragenesis in nature, we constructed a P-T diagram in the model system MgO-Al₂O₃-SiO₂-H₂O (MASH) for seven phases quartz (Qtz), B-free kornerupine sensu stricto, anthophyllite (Ath), chlorite (Chl), cordierite (Crd), kyanite (Ky), and talc. The minimum pressure for Krn + Tlc + Ky stability in MASH is close to that for Ky + Tlc stability, i.e., 6–8 kbar, at T≤ 780 °C. However, in the natural system, B₂O₃ and Na₂O are major constituents in Krn and orthoamphibole (Oam), respectively, and dravitic tourmaline (Tur) is widespread. The critical assemblage alternative to Krn + Tlc in nature is Tur + Oam. The upper pressure limit of Tur + Ath is determined by the upper pressure for anthophyllite: 7.7–10.5 kbar at 682–794 °C in the MgO-SiO₂-H₂O system (Chernosky et al. 1985, Am Mineral 70:223–236), and is undoubtedly higher in the presence of Na₂O, CaO, and Al₂O₃. At three of the six localities, talc is a retrograde phase; nonetheless, it possibly equilibrated with kornerupine on the retrograde path or during a later metamorphic event at P-T conditions appropriate for Ky + Tlc. At the sixth locality (Mulvoj, southwestern Pamir Mountains, Tajikistan), Krn is found in the same thin section as talc and kyanite and all three minerals formed during a prograde metamorphic event at T≥ 650 °C, P near 7 kbar. However, Krn is restricted to a lens 4 to 6 mm thick of phlogopite + anthophyllite + Tur and it does not touch either talc or kyanite. A reaction relating the Mulvoj and Chilapila Hill (Krn + Tlc + Ky + Qtz + Tur) parageneses is calculated from compositions in the Mulvoj rock to be 0.40Tur + 2.55Ath + 1.33H₂O + 0.27F = Krn + 2.16Tlc + 0.36B₂O₃ + 0.02Rutile + 0.19Na₂O + 0.17CaO. Given the difference in metamorphic pressures estimated for Mulvoj and Chilapila Hill, Krn + Tlc is inferred to be favored by increasing pressure as well as by low Na₂O and CaO contents. Some FeO, F, Fe₂O₃, and BeO are present in measurable amounts in at least one of the phases in the Mulvoj and Chilapila Hill whiteschists (e.g., Krn contains 0.24–0.67 wt% BeO), but the effect of these constituents is subordinate to that of Na₂O, CaO and B₂O₃. The Krn + Tlc could be a more important assemblage in B-bearing whiteschists than has been reported to date, particularly at pressures where orthoamphibole is no longer stable. Received: 21 April 1997 / Accepted: 13 October 1997     

Metamorphic reactions between fluid inclusions and mineral hosts. I. Progress of the reaction calcite+quartz=wollastonite+CO2 in natural wollastonite-hosted fluid inclusions

 At the Bufa del Diente contact-metamorphic aureole, brine infiltration through metachert layers embedded in limestones produced thick wollastonite rims, according to Cc+Qz=Wo+CO₂. Fluid inclusions trapped in recrystallized quartz hosts include: (1) high salinity four phase inclusions [Th(V-L)=460–573° C; Td(salts)=350–400° C; (Na+K)_Cleq=64–73 wt%; X _{CO 2}≤0.02]; (2) low density vapour-rich CO₂-bearing inclusions [Th(L-V)≈500±100° C; X _{CO 2}=0.22–0.44; X _NaCl≤0.01], corresponding to densities of 0.27± 0.05 gcm⁻³. Petrographical observations, phase compositions and densities show that the two fluids were simultaneously trapped in the solvus of the H₂O-CO₂-salts system at 500–600° C and 700±200 bars. The low density fluid was generated during brine infiltration at the solvus via the wollastonite producing reaction. Identical fluid types were also trapped as inclusion populations in wollastonite hosts 3 cm adjacent to quartz crystals. At room temperature, both fluid types additionally contain one quartz and one calcite crystal, generated by the back-reaction Wo+CO₂=Cc+Qz of the host with the CO₂-proportion of the fluid during retrogression. All of the CO₂ was removed from the fluid. On heating in the microstage, the reaction progress of the prograde reaction was estimated via volume loss of the calcites. In vapour-rich fluids, 50% progress is reached at 490–530° C; 80% at 520–560° C; and 100% at 540–590° C, the latter representing the trapping temperatures of the original fluid at the two fluid solvus. The progress is volume controlled. With knowledge of compositions and densities from unmodified inclusions in quartz and using the equation of state of Duan et al. (1995) for H₂O-CO₂-NaCl, along with f _{CO 2}-values extracted from it, the reaction progress curve was recalculated in the P-T-X-space. The calculated progress curve passes through the two fluid solvus up to 380° C/210 bars, continues in the one fluid field and meets the solvus again at trapping conditions. The P-T slope is steep, most of the reaction occurs above 450° C and there is high correspondence between calculated and measured reaction progress. We emphasize that with the exception of quartz, back-reactions between inclusion fluids and mineral hosts is a common process. For almost any prograde metamorphic mineral that was formed by a devolatilization reaction and that trapped the equilibrium fluid or any peak metamorphic fluid as an inclusion, a fluid-host back-reaction exists which must occur somewhere along the retrograde path. Such retrograde reactions may cause drastic changes in density and composition of the fluid. In most cases, however, evidence of the evolving mineral assemblages is not given for they might form submicroscopical layers at the inclusion walls. Received: 15 March 1995 / Accepted: 1 June 1995     

Global regression relations for conversion of surface wave and body wave magnitudes to moment magnitude

A homogenous earthquake catalog is a basic input for seismic hazard estimation, and other seismicity studies. The preparation of a homogenous earthquake catalog for a seismic region needs regressed relations for conversion of different magnitudes types, e.g. m _b , M _s , to the unified moment magnitude M _w. In case of small data sets for any seismic region, it is not possible to have reliable region specific conversion relations and alternatively appropriate global regression relations for the required magnitude ranges and focal depths can be utilized. In this study, we collected global events magnitude data from ISC, NEIC and GCMT databases for the period 1976 to May, 2007. Data for m_b magnitudes for 3,48,423 events for ISC and 2,38,525 events for NEIC, M _s magnitudes for 81,974 events from ISC and 16,019 events for NEIC along with 27,229 M _w events data from GCMT has been considered. An epicentral plot for M _w events considered in this study is also shown. M _s determinations by ISC and NEIC, have been verified to be equivalent. Orthogonal Standard Regression (OSR) relations have been obtained between M _s and M _w for focal depths (h < 70 km) in the magnitude ranges 3.0 ≤ M _s  ≤ 6.1 and 6.2 ≤ M _s  ≤ 8.4, and for focal depths 70 km ≤ h ≤ 643 km in the magnitude range 3.3 ≤ M _s  ≤ 7.2. Standard and Inverted Standard Regression plots are also shown along with OSR to ascertain the validation of orthogonal regression for M _s magnitudes. The OSR relations have smaller uncertainty compared to SR and ISR relations for M _s conversions. ISR relations between m _b and M _w have been obtained for magnitude ranges 2.9 ≤ m _b  ≤ 6.5, for ISC events and 3.8 ≤ m _b  ≤ 6.5 for NEIC events. The regression relations derived in this study based on global data are useful empirical relations to develop homogenous earthquake catalogs in the absence of regional regression relations, as the events catalog for most seismic regions are heterogeneous in magnitude types.     

Formation and destruction of periclase by fluid flow in two contact aureoles

Periclase formed in steeply dipping marbles from the Beinn an Dubhaich aureole, Scotland, and the Silver Star aureole, Montana, by the reaction dolomite = periclase + calcite + CO₂. Equilibrium between rock and fluids with X _{CO 2} < 1 requires that reaction was infiltration-driven. Brucite pseudomorphs after periclase occur in the Beinn an Dubhaich aureole either as bed-by-bed replacement of dolomite or in a lens along the contact between dolomite and a pre-metamorphic dike. Transport theory predicts that infiltration drove both periclase reaction and ¹⁸O-depletion fronts which moved at significantly different velocities along the flow path. The distributions of brucite and ¹⁸O-depleted rocks are identical in surface exposures, thus indicating upward flow. Time-integrated flux (q) was <500 mol/cm² and the fluid source was magmatic. Because periclase and its hydrated equivalent brucite are unaltered to dolomite by retrograde reactions, the exposure of brucite marbles accurately images the flow paths of peak metamorphic fluids. In the Silver Star aureole brucite pseudomorphs after periclase exclusively occur in tabular bodies that are beds with elevated Mg/Ca. The spatial pattern of ¹⁸O-depletion requires upward vertical fluid flow. Estimated prograde q ≈ 10³–10⁴ mol/cm² and the fluid source was magmatic. Low Mg/Ca, ¹⁸O-depleted, brucite-free rocks pose a dilemma because the periclase reaction front should have traveled ≈18 times further through them than the isotope alteration front. The dilemma is resolved by reaction textures that indicate periclase and brucite were destroyed in low Mg/Ca rocks by infiltration-driven retrograde carbonation reactions. Values of retrograde q were ≈10³–10⁴ mol/cm². Brucite (after periclase) was preserved only in high Mg/Ca layers where periclase developed in greater abundance. The geometry of brucite marbles at Silver Star thus reflects the location of high Mg/Ca beds rather than the geometry of fluid flow. Retrograde reactions must be considered before the mineralogical record of prograde fluid flow can correctly be interpreted. In both aureoles fluid flow, mineral reaction, and isotope depletion were structurally controlled by bedding and lithologic contacts. Received: 30 July 1996 / Accepted: 21 March 1997     

Prograde and Retrograde Eclogites in the Sambagawa Metamorphic Belt, Besshi District, Japan

In the Besshi district of the Sambagawa metamorphic belt, thereare two types of eclogites: one occurring in the Sebadani metagabbromass and retrograded from high-temperature anhydrous ecologite,and the other in the basic schists and produced by prograde,dehydration of epidote amphibolite. The Sebadani metagabbro mass was originally layered gabbro,which was once equilibrated in the ecologite facies before emplacementinto the Sambagawa terrain as a hot eclogite mass. Basic schistssurrounding the Sebadani mass, which had suffered the Sambagawametamorphism of albite epidote amphibolite facies, were contact-metamorphosedat high pressure by the emplacement of the Sebadani mass. Asa result, the basic schists were dehydrated to form eclogiticbasic schists, i.e. garnet and omphacite porphyroblast-bearingbasic schists. Thus, two types of ecologite, retrograde andprograde, converged into the same metamorphic condition, 610–650?C, 7–17 kb, in a part of the ecologite facies duringthe Sambagawa metamorphism. Correspondingly, the values of distributioncoefficients of Fe and Mg between garnet and omphacite increasefrom core pairs to rim pairs in the retrograde eclogites anddecrease from core pairs to rim pairs in the prograde ecologites.After this stage, both the prograde and retrograde eclogitesshared a common metamorphic history; they were retrograded viathe epidote amphibolite facies to the greenschist facies. The Sebadani metagabbro mass, as a large tectonic block, hadbeen emplaced into a m?lange zone in the Sambagawa metamorphicbelt after the peak of the Sambagawa metamorphism, probablyfollowing initiation of uplift of the metamorphic rocks fromtheir deep-seated environment.     

Detrital,metamorphic and metasomatic tourmaline in high-pressure metasediments from Syros (Greece): intra-grain boron isotope patterns determined by secondary-ion mass spectrometry

The boron isotopic composition of zoned tourmaline in two metasediments from the island of Syros, determined by secondary-ion mass spectrometry (SIMS), reflects the sedimentary and metamorphic record of the rocks. Tourmaline from a silicate-bearing marble contains small (≤20 μm) detrital cores with highly variable δ ¹¹B values (−10.7 to +3.6‰), pointing to a heterogeneous protolith derived from multiple sources. The sedimentary B isotopic record survived the entire metamorphic cycle with peak temperatures of ∼500°C. Prograde to peak metamorphic rims are homogeneous and similar among all analysed grains (δ ¹¹B ≈ +0.9‰). The varying δ ¹¹B values of detrital cores in the siliceous marble demonstrate that in situ B isotope analysis of tourmaline by SIMS is a potentially powerful tool for provenance studies not only in sediments but also in metasediments. A meta-tuffitic blueschist bears abundant tourmaline with dravitic cores of detrital or authigenic origin (δ ¹¹B ≈ −3.3‰), and prograde to peak metamorphic overgrowth zones (−1.6‰). Fe-rich rims, formed during influx of B-bearing fluids under retrograde conditions, show strongly increasing δ ¹¹B values (up to +7.7‰) towards the margins of the grains. The δ ¹¹B values of metamorphic tourmaline from Syros, formed in mixed terrigenous–marine sediments, reflect the B signal blended from these two different sources, and was probably not altered by dehydration during subduction.     

P -T paths from anatectic pelites

A relatively simple petrogenetic grid for partial melting of pelitic rocks in the NCKFMASH system is presented based on the assumption that the only H₂O available for melting is through dehydration reactions. The grid includes both discontinuous and continuous Fe-Mg reactions; contours of Fe/(Fe+Mg) for continuous reactions define P-T vectors along which continuous melting will occur. For biotite-bearing assemblages (garnet+biotite + sillimanite + K-feldspar + liquid and garnet + biotite + cordierite + K-feldspar + liquid), Fe/(Fe+Mg) contours have negative slopes and melting will occur with increasing temperature or pressure. For biotite-absent assemblages (garnet + cordierite + sillimanite + K-feldspar + liquid or garnet + cordierite + orthopyroxene + K-feldspar + liquid) Fe/(Fe + Mg) contours have flat slopes and melting will occur only with increasing pressure. The grid predicts that abundant matrix K-feldspar should only be observed if rocks are heated at P < 3.8 kbar, that abundant retrograde muscovite should only be observed if rocks are cooled at P > 3.8 kbar, and that generation of late biotite + sillimanite replacing garnet, cordierite, or as selvages around leu- cosomes should be common in rocks in which melt is not removed. There is also a predicted field for dehydration melting of staurolite between 5 and 12 kbar. Textures in migmatites from New Hampshire, USA, suggest that prograde dehydration melting reactions are very nearly completely reversible during cooling and crystallization in rocks in which melt is not removed. Therefore, many reaction textures in “low grade” migmatites may represent retrograde rather than prograde reactions. Received: 5 March 1998 / Accepted: 7 August 1998     

Differences in grain growth of calcite: a field-based modeling approach

Normal grain growth of calcite was investigated by combining grain size analysis of calcite across the contact aureole of the Adamello pluton, and grain growth modeling based on a thermal model of the surroundings of the pluton. In an unbiased model system, i.e., location dependent variations in temperature-time path, 2/3 and 1/3 of grain growth occurs during pro- and retrograde metamorphism at all locations, respectively. In contrast to this idealized situation, in the field example three groups can be distinguished, which are characterized by variations in their grain size versus temperature relationships: Group I occurs at low temperatures and the grain size remains constant because nano-scale second phase particles of organic origin inhibit grain growth in the calcite aggregates under these conditions. In the presence of an aqueous fluid, these second phases decay at a temperature of about 350 °C enabling the onset of grain growth in calcite. In the following growth period, fluid-enhanced group II and slower group III growth occurs. For group II a continuous and intense grain size increase with T is typical while the grain growth decreases with T for group III. None of the observed trends correlate with experimentally based grain growth kinetics, probably due to differences between nature and experiment which have not yet been investigated (e.g., porosity, second phases). Therefore, grain growth modeling was used to iteratively improve the correlation between measured and modeled grain sizes by optimizing activation energy (Q), pre-exponential factor (k₀) and grain size exponent (n). For n=2, Q of 350 kJ/mol, k₀ of 1.7×10²¹ mⁿs^–1 and Q of 35 kJ/mol, k₀ of 2.5×10^-5 mⁿs^–1 were obtained for group II and III, respectively. With respect to future work, field-data based grain growth modeling might be a promising tool for investigating the influences of secondary effects like porosity and second phases on grain growth in nature, and to unravel differences between nature and experiment.Editorial responsibility: J. Hoefs     

P-T paths and tectonic evolution of shear zones separating high-grade terrains from cratons: examples from Kola Peninsula (Russia) and Limpopo Region (South Africa)

Summary ?The petrology and P-T evolution of mica schists from two regional scale tectonic (shear) zones that separate high grade terrains (“mobile belts”) from cratons are described. These are the 2.4–1.9 Ga Tanaelv Belt, a suture zone that separates the Lapland granulite complex from the Karelian craton (Kola Peninsula–Fennoscandia), and the 2.69 Ga Hout River Shear Zone that separates the > 2.9 Ga Kaapvaal craton from the 2.69 Ga South Marginal Zone of the Limpopo high-grade terrain (South Africa). Two metamorphic zones are identified in strongly deformed mica schists from the 1.9 Ga Korva Tundra Group of the Tanaelv belt: (1) a chlorite-staurolite zone tectonically overlaying gneisses of the Karelian craton, and (2) a kyanite-biotite zone tectonically underlying garnet amphibolites of the Tanaelv Belt, which are in tectonic contact with the Lapland granulite complex. The prograde reaction Chl+St+Ms ↠ Ky+Bt+Qtz+H₂O clearly defines a boundary between zones (1) and (2). Rotated garnet porphyroblasts from zone (1) contain numerous inclusions (Otz, Chl, Ms), and show clear Mg/Fe chemical zoning, suggesting garnet growth during prograde metamorphism. The metamorphic peak, T = 650°C and P = 7.5 kbar, is recorded in the kyanite-biotite zone and characterized by unzoned snowball garnet. In many samples of mica schists euhedral garnet porphyroblasts of the retrograde stage are completely devoid of mineral inclusions while N _Mg decreases from core to rim, indicating a decrease in P-T from 650°C, 7.5 kbar to 530°C, 5 kbar. The Hout River Shear Zone (South Africa) shows metamorphic zonation from greenschists through epidote amphibolites to garnet amphibolites. Rare strongly deformed mica schists (Chl+Grt+Pl+Ms+Bt+Qtz) occur as thin layers among epidote-amphibolites only. Garnet porphyroblasts in the schists are similar to that of the Tanaelv Belt recording a prograde P-T path with peak conditions of T = 600°C and P∼ 5.5 kbar. The retrograde stage is documented by the continuous reaction Prp+2Ms+Phl ↠ 6Qtz+3East recording a minimum T = 520°C and P ∼ 3.3 kbar. Similar narrow clock-wise P-T loops recorded in mica schists from both studied shear zones suggest similarities in the geodynamic history of both shear zones under consideration.

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Zusammenfassung ?P-T Pfade und tektonische Entwicklung von Scherzonen, die hochgradige Terranes von Kratonen trennen: Zwei Beispiele von der Halbinsel Kola (Russland) und der Limpopo-Region (Südafrika) Die Petrologie und P-T Entwicklung von Glimmerschiefern aus zwei regionalen tektonischen Scherzonen, die hochgradige Terranes (“mobile belts”) von Kratonen trennen, werden beschrieben. Diese sind der 2.4−1.9 Ga Tanaev Belt, eine Suturzone, die die Lappland Granulite vom karelischen Pluton (Halbinsel Kola - Fennoskandien) trennt, sowie die 2.69 Ga Hout River Shear Zone, die den > 2.9 Ga Kaapvaal Kraton von der 2.69 Ga South Marginal Zone des hochgradigen Limpopo Terranes (Südafrika) trennt. Zwei metamorphe Zonen sind in stark deformierten Glimmerschiefern der 1.9 Ga Korva Tundra Group zu unterscheiden: (1) eine Chlorit-Staurolith-Zone, die den Gneisen des karelischen Kratons auflagert, und (2) eine Kyanit-Biotit-Zone, die die Granatamphibolite des Tanaev Belt unterlagert und in tektonischem Kontakt mit dem Lappland Granulitkomplex steht. Die prograde Reaktion Chl+St+Ms ↠ Ky+Bt+Qtz+H₂O trennt die beiden Zonen. Rotierte Granatporphyroblasten aus der Zone (1) enthalten zahlreiche Einschlüsse (Qtz, Chl, Ms) und zeigen eine Mg/Fe Zonierung, die Granatwachstum w?hrend des prograden Metamorphosestadiums nahelegen. Der Metamorphoseh?hepunkt (650°C, 7.5 kbar) wurde in der Kyanit-Biotit-Zone erreicht und ist durch nicht zonierte Schneeballgranate charakterisiert. In vielen Glimmerschieferproben sind die euhedralen Granatporphyroblasten des retrograden Stadiums vollkommen einschlu?frei und N _Mg nimmt vom Kern zum Rand hin ab. Das zeigt eine Abnahme der P-T Bedingungen von 650°C, 7.5 kbar auf 530°C, 5 kbar an. Die Hout River Shear Zone in Südafrika zeigt eine metamorphe Zonierung von Grünschiefern, über Epidotamphibolite zu Granatamphiboliten. Selten kommen stark deformierte Glimmerschiefer (Chl+Grt+Pl+Ms+Bt+Qtz) als dünne Lagen zwischen den Epidotamphiboliten vor. Die Granatporphyroblasten sind ?hnlich wie die aus dem Tanaev Belt und belegen eine prograde P-T Entwicklung mit Peak-Bedingungen von 600°C und ≈ 5.5 kbar. Das retrograde Stadium ist durch die kontinuierliche Reaktion Prp+2Ms+Phl ↠ 6Qtz+3East mit minimal 530°C und ≈ 3.3 kbar dokumentiert. Die sehr ?hnlichen P-T Pfade der Glimmerschiefer belegen ?hnlichkeiten in der geodynamischen Geschichte der beiden bearbeiteten Scherzonen.

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Received January 29, 1999;/revised version accepted August 10, 1999     

Subduction-related P–T path for eclogites and garnet glaucophanites from the Samaná Peninsula basement complex, northern Hispaniola

Eclogite and garnet glaucophanite lenses from the Punta Balandra unit of the Samaná basement complex (northern Hispaniola) preserve information of the early metamorphic and tectonic history of subduction in the Caribbean island-arc and its collision with the North America plate. For this reason, P–T paths were reconstructed from the interpretation of meso- and microfabrics, mineral assemblages and chemistry, with the aid of equilibrium phase diagrams calculated for specific bulk compositions in the CKNFMASH system and isopleths for selected solution end-members. The obtained results suggest that the subduction-related prograde path evolved from garnet-free and garnet-bearing lawsonite-blueschist facies, to phengite eclogite facies conditions at P=22–24 kbar and T=610–625°C, with a probable intermediate stage of low-P lawsonite eclogite facies. The subsequent retrograde P–T path entered the epidote-blueschist (garnet-free) facies and ended within the greenschist facies field, similar to the prograde evolution at low-P. Eclogites and garnet glaucophanites formed in a subduction zone in which oceanic lithosphere was subducted WSW/W beneath the Caribbean plate.     

Prograde and retrograde fluid flow during contact metamorphism of siliceous carbonate rocks from the Ballachulish aureole,Scotland

 Siliceous dolomites and limestones contain abundant retrograde minerals produced by hydration-carbonation reactions as the aureole cooled. Marbles that contained periclase at the peak of metamorphism bear secondary brucite, dolomite, and serpentine; forsterite-dolomite marbles have retrograde tremolite and serpentine; wollastonite limestones contain secondary calcite and quartz; and wollastonite-free limestones have retrograde tremolite. Secondary tremolite never appears in marbles where brucite has replaced periclase or in wollastonite-bearing limestones. A model for infiltration of siliceous carbonates by CO₂-H₂O fluid that assumes (a) vertical upwardly-directed flow, (b) fluid flux proportional to cooling rate, and (c) flow and reaction under conditions of local equilibrium between peak temperatures and ≈400 °C, reproduces the modes of altered carbonate rocks, observed reaction textures, and the incompatibility between tremolite and brucite and between tremolite and wollastonite. Except for samples from a dolomite xenolith, retrograde time-integrated flux recorded by reaction progress is on the order of 1000 mol fluid/cm² rock. Local focusing of flow near the contact is indicated by samples from the xenolith that record values an order of magnitude greater. Formation of periclase, forsterite, and wollastonite at the peak of metamorphism also required infiltration with prograde time-integrated flux approximately 100–1000 mol/cm². The comparatively small values of prograde and retrograde time-integrated flux are consistent with lack of stable isotope alteration of the carbonates and with the success of conductive thermal models in reproducing peak metamorphic temperatures recorded by mineral equilibria. Although isobaric univariant assemblages are ubiquitous in the carbonates, most formed during retrograde metamorphism. Isobaric univariant assemblages observed in metacarbonates from contact aureoles may not record physical conditions at the peak of metamorphism as is commonly assumed. Received: 19 September 1995 / Accepted: 14 March 1996     

Global spectra of energy and enstrophy and their fluxes during July 1979

Transient and stationary spectra of kinetic energy (KE), available potential energy (APE) and enstrophy (EN), and their spectral fluxes as a function of the two-dimensional wavenumbern were computed for July 1979. Triangular truncation at zonal wavenumber 42 was used for computation. The slopes of various spectra in the wavenumber range 14≤n≤25 were obtained by fitting a straight line in log-log scale by the least square method. The transientKE, APE andEN spectra in the lower (upper) troposphere had slopes −2·21 (−2·30), −2·65 (−2·64) and −0·36 (−0·46), respectively. The effect of stationary and divergent motion on the slope values was investigated. The possible correlation between the slope and percentage of transient component in the combined energy and enstrophy was examined to identify the transient motion of the atmosphere with the two-dimensional homogeneous isotropic turbulence. The vertically averaged slope of kinetic energy and enstrophy in the lower (upper) troposphere was close to the value at 700 (200) hPa level. The spectral fluxes of kinetic energy and enstrophy in the wavenumber range 14≤n≤25 satisfied, to a very rough approximation, the criteria of inertial subrange. The stationary fluxes were small. The estimated stationary-transient component of flux was larger, comparable and less than the corresponding transient flux of APE, KE and EN. Representative levels for computation of energy and enstrophy spectra and their fluxes in the lower and upper troposphere were identified.     

Thermal expansion and structural transformations of stuffed derivatives of quartz along the LiAlSiO4–SiO2 join: a variable-temperature powder synchrotron XRD study

 The structural behavior of stuffed derivatives of quartz within the Li_{1− x} Al_{1− x} Si_{1+ x} O₄ system (0 ≤ x ≤ 1) has been studied in the temperature range 20 to 873 K using high-resolution powder synchrotron X-ray diffraction (XRD). Rietveld analysis reveals three distinct regimes whose boundaries are defined by an Al/Si order-disorder transition at x=∼0.3 and a β–α displacive transformation at x=∼0.65. Compounds that are topologically identical to β-quartz (0 ≤ x < ∼0.65) expand within the (0 0 1) plane and contract along c with increasing temperature; however, this thermal anisotropy is significantly higher for structures within the regime 0 ≤ x < ∼0.3 than for those with compositions ∼0.3 ≤ x < ∼0.65. We attribute this disparity to a tetrahedral tilting mechanism that occurs only in the ordered structures (0 ≤ x < ∼0.3). The phases with ∼0.65 ≤ x ≤ 1 adopt the α-quartz structure at room temperature, and they display positive thermal expansion along both a and c from 20 K to their α–β transition temperatures. This behavior arises mainly from a rotation of rigid Si(Al)-tetrahedra about the <100> axes. Landau analysis provides quantitative evidence that the charge-coupled substitution of Li+Al for Si in quartz dampens the α–β transition. With increasing Li+Al content, the low-temperature modifications exhibit a marked decrease in spontaneous strain; this behavior reflects a weakening of the first-order character of the transition. In addition, we observe a linear decrease in the α–β critical temperature from 846 K to near 0 K as the Li+Al content increases from x=0 to x=∼0.5. Received: 26 June 2000 / Accepted: 1 December 2000     

The geochemistry of prograde and retrograde charnockite-gneiss reactions in southern India

Exposures in many quarries in southern India exhibit field evidence for incipient charnockitization of tonalitic and granitic gneiss (prograde relationship), or retrogression of charnockite to produce tonalitic gneiss (retrograde relationship). Few systematic geochemical relationships exist between adjacent gneisscharnockite sample pairs during either prograde or retrograde reactions. Most elements and element ratios exhibit inconsistent variations; however, prograde chamockites appear enriched in Ta, Pb, volatiles (chiefly CO₂), and in transition metals relative to Mg, and depleted in REE and Y compared to adjacent gneiss protoliths. Retrograde gneisses have higher Rb, Pb, Th, Hf, Zn relative to Co, Nb relative to Ta, Hf relative to Zr, and volatiles (chiefly H₂O) compared to parental charnockites. Of those elements (U, Th, Rb, Cs, Pb) significantly depleted in high-pressure charnockites exposed south of the prograde transition zone, only Pb is significantly replenished during retrogression. Evidence suggests that prograde fluids are relatively rich in CO₂ and retrograde fluids in H₂O and that the typical non-systematic geochemical variations during prograde and retrograde reactions reflect local effects at the wave front.     

Variation of the oxygen content and point defects in olivines, (Fe x Mg 1−x )2SiO4, 0.2 ≤ x ≤ 1.0

 The variation of the oxygen content in olivines, (Fe _x Mg_{1− x} )₂SiO₄, with 0.2 ≤ x ≤ 1.0, was investigated by thermogravimetric measurements. Mass changes occurring upon oxygen activity changes were measured as a function of oxygen activity and cationic composition at 1130 and 1200 °C. During the measurements the samples were in direct contact with gases containing CO, CO₂ and N₂ and, at a few spots at the bottom of the sample stack, also with SiO₂. By fitting experimental data of mass changes to equations derived using point defect thermodynamics, it was shown for olivines with 0.2 ≤ x ≤ 1.0 at 1130 °C and 0.2 ≤ x ≤ 0.7 at 1200 °C within the oxygen activity ranges investigated that the observed variations in the oxygen contents are compatible with cation vacancies and Fe³⁺ ions on M sites and Fe³⁺ ions on silicon sites as majority defects if it is assumed that only three types of point defects occur as majority defects. Different cases were considered, closed systems, taking into account that ξ=[Si]/([Si]+[Fe]+[Mg]) is not necessarily equal to 1/3, and olivines in equilibrium with SiO₂ or pyroxenes. The oxygen content variations observed in this study are significantly smaller than those reported previously in the literature. It is proposed that these differences are related to the dissolution of Fe into noble metal containers used as sample holders in earlier studies and/or to the presence of secondary phases. Received: 1 November 1995 / Accepted: 15 September 2002 Acknowledgements This work was supported by the Cornell Center for Materials Research (CCMR), a Materials Research Science and Engineering Center of the National Science Foundation (DMR-0079992). The authors thank Mr. Daniel M. DiPasquo and Mr. Jason A. Schick for helping in experimental work.     

Prograde and retrograde fluid-rock interaction in calc-silicates northwest of the Idaho batholith: stable isotopic evidence

Carbon and oxygen isotopic analyses of silicate and carbonate minerals indicate that isotopic compositions in metasediments of the Wallace Formation (Belt Supergroup) exposed northwest of the Idaho batholith have been affected by both prograde and retrograde fluid-rock interaction. Silicates retain isotopic fractionations that reflect equilibration at peak metamorphic temperatures. In contrast, calcite oxygen isotopic compositions range from δ¹⁸O(Calcite)=+2.3 to +18.6‰ SMOW (standard mean oceanic water) and indicate that some calcites have exchanged with low-δ¹⁸O meteorichydrothermal fluids. Values of Δ¹⁸O (Quartz-Calcite) as large as +15.5 clearly indicate that the isotopic depletion of these calcites postdates the peak of regional metamorphism. Carbon isotopic compositions of ¹⁸O-depleted calcites are not significantly shifted relative to δ¹³C values in undepleted calcites, suggesting that the retrograde fluid was carbon-poor. Petrographically, retrograde fluid-rock interaction is associated with the occurrence of fine-grained, highly-luminescent calcite overgrowths on less-luminescent, metamorphic calcites, slight to moderate argillic alteration, and pseudomorphing of scapolite porphyroblasts by fine-grained albite. Retrograde isotopic depletions may be related to shallow meteoric-hydrothermal fluid flow developed around the Idaho batholith after intrusion and rapid uplift of the terrane. Peak metamorphic isotopic compositions in the Wallace Formation reflect mineralogically heterogeneous protolith compositions and isotopic fractionation due to devolatilization and/or infiltration. Variability in oxygen isotopic compositions on the order of 4–6‰ within the same rock type can be attributed to the combined effects of inherited isotopic compositions and isotopic shifts resulting from prograde devolatilization. Isotopic and compositional heterogeneity on the scale of mm to m precludes generalization of isotopic gradients on a regional scale. The isotopic data presented here, and metamorphic fluid compositions determined in previous studies, are best reconciled with heterogeneous bulk compositions, dominantly channelized prograde and retrograde fluid flow, and locally low fluid-rock ratios.