NASA Astrophysics Data System (ADS)
Richter, B.; Stünitz, H.; Heilbronner, R.
2016-11-01
Coesite was found in quartz aggregates, experimentally deformed at confining pressures of 1.0-1.5 GPa and temperatures between 600°C and 900°C. The confining pressure (Pc) and, in most cases, the mean stress (σm) of the experiments were below those of the quartz-to-coesite phase transformation. Yet coesite formed when the maximum principal stress (σ1) was within the P-T range of the coesite stability field. In one sample, the euhedral coesite grains were corroded indicating that coesite started to transform back to quartz. It is inferred that this sample started to deform with σ1 above the quartz-to-coesite phase transformation and, with ongoing deformation, σ1 decreased to values in the quartz stability field due to strain weakening. In all cases, σ1 triggered the quartz-to-coesite reaction as well as the reverse reaction, suggesting that σ1 is the critical parameter for the quartz-to-coesite transformation—not Pc or σm. With progressive deformation, the coesite laths rotated toward the shear plane as more rigid particles with the sense of shear. In case of back reaction, new quartz grains exhibit no systematic crystallographic relationship with respect to old coesite. The experiments cover different degrees of pressure "overstepping," different temperatures, and different experimental durations at P and T, and deformation always enhances the reaction kinetics. The observation that σ1 is critical for a pressure-dependent phase transformation (also for reversals) poses questions for the thermodynamic treatment of such phase transformations.
NASA Astrophysics Data System (ADS)
Wang, L.; Wang, S.; Brown, M.
2016-12-01
In contrast to coesite that occurs as inclusions in zircon and rock-forming minerals, intergranular coesite is preserved in UHP eclogite at Yangkou in the Sulu belt. The survival of intergranular coesite is intriguing because the eclogite experienced phengite growth and partial melting during exhumation. The coesite eclogite occurs as rootless isoclinal fold noses within quartz-rich schist which contains 10-20 vol% phengite, whereas phengite is absent from coesite eclogite in the fold noses. To evaluate the factors that control preservation of intergranular coesite, four samples representative of different stages along the retrograde P-T path were selected for study. For each sample we determined the number of intergranular coesite grains per cm2 and the OH content of garnet and omphacite. As the number of coesite grains decreases, the bulk rock OH content increases from <200 ppm in phengite-free coesite eclogite to 200-260 ppm in phengite-bearing (<5 vol%) coesite eclogite and up to a maximum of 430-438 ppm in quartz eclogite ( 10 vol% phengite). However, the OH content drops to a minimum of 59 ppm in residual eclogite resulting from melt drainage. This trend implies that the volume of fluid increased sufficiently during exhumation to facilitate the growth of phengite and the transformation to quartz of intergranular coesite outside of the fold noses. The fluid is inferred to have been a supercritical fluid probably residual from prograde dehydration but also derived by dissolution of nominally anhydrous minerals. Post-metamorphic-peak deformation combined with fluid percolation along sheared fold limbs induced phengite growth during initial exhumation and then facilitated partial melting. In contrast, fold hinges in competent layers are unfavourable sites for fluid penetration. At Yangkou, the intergranular coesite is preserved in the fold noses where it was protected from both penetrative deformation and fluid ingress. Therefore, the fold noses maintained a relatively dry environment that allowed preservation of the intergranular coesite. Thus, deformation partitioning and strain localization impose local controls on fluid distribution and migration in UHP eclogite. This study informs our understanding of variations in fluid regime during exhumation of deeply subducted continental crust.
Hemingway, B.S.; Bohlen, S.R.; Hankins, W.B.; Westrum, E.F.; Kuskov, O.L.
1998-01-01
The heat capacities of synthetic coesite and jadeite were measured between about 15 and 850 K by adiabatic and differential scanning calorimetry. The experimental data were smoothed and estimates were made of heat capacities to 1800 K. The following equations represent our estimate of the heat capacities of coesite and jadeite between 298.15 and 1800 K: [see original article for formula]. Tables of thermodynamic values for coesite and jadeite to 1800 K are presented. The entropies of coesite and jadeite are 40.38 ?? 0.12 and 136.5 ?? 0.32 J/(mol.K), respectively, at 298.15 K. The entropy for coesite derived here confirms the value published earlier by Holm et al. (1967). We have derived an equation to describe the quartz-coesite boundary over the temperature range of 600 to 1500 K, P(GPa) = 1.76 + 0.001T(K). Our results are in agreement with the enthalpy of transition reported by Akaogi and Navrotsky (1984) and yield -907.6 ?? 1.4 kJ/mol for the enthalpy of formation of coesite from the elements at 298.15 K and 1 bar, in agreement with the value recommended by CODATA (Khodakovsky et al. 1995). Several sources of uncertainty remain unacceptably high, including: the heat capacities of coesite at temperatures above about 1000 K; the heat capacities and volumetric properties of ?? quartz at higher pressures and at temperatures above 844 K; the pressure corrections for the piston cylinder apparatus used to determine the quartz-coesite equilibrium boundary.
Coesite in suevites from the Chesapeake Bay impact structure
Jackson, John C.; Horton, J. Wright; Chou, I-Ming; Belkin, Harvey E.
2016-01-01
The occurrence of coesite in suevites from the Chesapeake Bay impact structure is confirmed within a variety of textural domains in situ by Raman spectroscopy for the first time and in mechanically separated grains by X-ray diffraction. Microtextures of coesite identified in situ investigated under transmitted light and by scanning electron microscope reveal coesite as micrometer-sized grains (1–3 μm) within amorphous silica of impact-melt clasts and as submicrometer-sized grains and polycrystalline aggregates within shocked quartz grains. Coesite-bearing quartz grains are present both idiomorphically with original grain margins intact and as highly strained grains that underwent shock-produced plastic deformation. Coesite commonly occurs in plastically deformed quartz grains within domains that appear brown (toasted) in transmitted light and rarely within quartz of spheroidal texture. The coesite likely developed by a mechanism of solid-state transformation from precursor quartz. Raman spectroscopy also showed a series of unidentified peaks associated with shocked quartz grains that likely represent unidentified silica phases, possibly including a moganite-like phase that has not previously been associated with coesite.
NASA Astrophysics Data System (ADS)
Sobolev, N.
2005-12-01
Inclusions in diamonds (DIs) represent an important source of information about the composition of continental lithospheric mantle. The isolated coesite inclusions in two diamonds (Harris, 1968) and a full set of eclogitic minerals (coesite (Cs), garnet (Ga), omphacite Cpx)) in two Yakutian diamonds (Sobolev et al., 1976), followed by finds of Cs-eclogite xenoliths (Smyth and Hatton, 1977; Ponomarenko et al., 1977) testify to the importance of coesite as a constituent of eclogitic rocks in deep lithospheric environment. Since these earlier times, coesite has been documented in more than 250 natural diamonds from 25 localities worldwide. Some 40 xenoliths of Cs-eclogites were found both in South African and Yakutian kimberlites. However, >50% of DIs of coesite are related to only four (4) diamond localities, including Guaniamo, Venezuela (Sobolev et al., 1998, 2003), Argyle (Jaques et al., 1989; Sobolev et al., 1989), New South Wales, all Australia (Sobolev et al., 1984; Meyer et al., 1997), and North Yakutian alluvials (Sobolev et al., 1999). All described DIs with coesite are from a wide range of assemblages: websterites to kyanite eclogites; grospydites and calcsilicate assemblages, with a large range in Gt [3.7-28.7 wt.% CaO] and Cpx [ 0.9-8.8 wt.% Na2O] compositions. In spite of these occurrences in diamonds, to the present, no coesite has been detected within the assemblage of minerals making up some 400 diamondiferous-eclogite xenoliths; similarly, no diamonds have been found in any Cs-eclogite xenoliths. This apparent paradox may be caused by coesite alteration in the diamondiferous eclogites, whereas coesite eclogites may have formed only outside of the diamond stability field. Indeed, coesite eclogites (without diamonds) may occupy a shallower position within continental lithosphere compared with the normal E-type diamond source. This indicates a broadly basaltic chemistry of the deep eclogitic environment, additional evidence for a protolith from the subduction of oceanic crust.
NASA Technical Reports Server (NTRS)
Weaver, J. S.; Chipman, D. W.; Takahashi, T.
1979-01-01
Phase stability and elasticity data have been used to calculate the Gibbs free energy, enthalpy, and entropy changes at 298 K and 1 bar associated with the quartz-coesite and coesite-stishovite transformations in the system SiO2. For the quartz-coesite transformation, these changes disagree by a factor of two or three with those obtained by calorimetric techniques. The phase boundary for this transformation appears to be well determined by experiment; the discrepancy, therefore, suggests that the calorimetric data for coesite are in error. Although the calorimetric and phase stability data for the coesite-stishovite transformation yield the same transition pressure at 298 K, the phase-boundary slopes disagree by a factor of two. At present, it is not possible to determine which of the data are in error. Thus serious inconsistencies exist in the thermodynamic data for the polymorphic transformations of silica.
Coesite from Wabar crater, near Al Hadida, Arabia
Chao, E.C.T.; Fahey, J.J.; Littler, J.
1961-01-01
The third natural occurrence of coesite, the high pressure polymorph of silica, is found at the Wabar meteorite crater, Arabia. The Wabar crater is about 300 feet in diameter and about 40 feet deep. It is the smallest of three craters where coesite has been found.
NASA Astrophysics Data System (ADS)
Sobolev, N. V.
2010-12-01
Coesite, a high-pressure polymorph of silica, was first discovered as part of a coesite-eclogite assemblage (coesite, garnet, omphacite) in equilibrium with diamond as diamond inclusion (DI) in Siberian diamond placers (Sobolev et al., 1976, Dokl. Akad. Nauk SSSR, 230: 1442). In recent years, coesite has become a key mineral coexisting with diamond both in kimberlite (DIs) and in UHP metamorphic rocks of the Kokchetav massif, Kazakhstan (diamondiferous gneisses and calcsilicate rocks). In the UHPM rocks of Kokchetav massif, coesite was first detected as inclusions in zircon associated with diamonds (Sobolev et al., 1991, Dokl. Akad. Nauk SSSR, 321: 184), as a result of the initial studies that had identified diamonds as inclusions in garnets and zircons (Sobolev, Shatsky, 1990, Nature, 343: 742). Garnet and omphacitic clinopyroxene are the principal primary minerals associated with coesite and diamond in UHP mantle and crustal rocks. Their compositions plot distinctly within the eclogitic compositional field and substantiate the existence of coesite presence as DIs in eclogitic (E-type) diamonds, as well as sometimes in xenoliths of diamondiferous eclogites (Shatsky et al., 2008, Lithos, 105:289). One of the major significant features of these eclogitic minerals in both UHPM and kimberlitic mantle occurrences is the K2O contents of the clinopyroxenes, reaching 1.6 wt.%, with Na2O and MnO in Ca-Mg-Fe garnets reaching 0.3 and 6.0 wt.%, respectively. Stable isotope data for C in diamonds and O in garnet, pyroxene and coesite have resulted in establishing a very wide range for these isotopes most typical for crustal conditions - i.e., atypical of mantle values. This is clearly shown for coesite DIs (Schulze et al., 2003, Nature, 428:68), garnets from diamondiferous eclogite xenoliths from Siberian kimberlites (Spetsius et al., 2008, Eur. J. Min., 20:375), garnets and clinopyroxenes from UHP calcsilicate diamondiferous rocks of the Kokchetav massif (Sobolev et al., in press, Contr. Min. Petr.). This extensive wide range in δ13C (PDB) for coesite-bearing diamonds, from -28 to +1.5 ‰, along with common crustal δ18O (SMOW) values from the principal rock-forming minerals (garnet and clinopyroxene) and accessory mineral (coesite), is typical for diamondiferous mantle eclogites, crustal UHPM rocks, and DIs. The petrogenetic evidences from all these rocks and minerals are indicative of major subduction of crustal protoliths (Ringwood, 1972, EPSL, 14:233), including the recycling of crustal carbon into diamonds in mantle eclogites, first speculated on by V.S. Sobolev and N.V. Sobolev (1980, Dokl. Akad. Nauk SSSR, 249: 1217).
On the preservation mechanism of intragranular coesite in the Yangkou, Sulu UHP eclogite
NASA Astrophysics Data System (ADS)
Wang, L.; Zhang, J.; Wang, S.; Shi, F.; Cen, Y.
2012-12-01
Yangkou Bay, in the Sulu ultrahigh-pressure (UHP) belt of eastern China is the only known locality in the world in which UHP eclogite contains intragranular coesite. The question remains then, how is the extremely rare occurrence of intragranular coesite preserved in the Sulu belt, and if we can identify the reasons for its preservation, might it be found in other UHP belts? Preservation of coesite inclusions or intragranular coesite has been interpreted to result from multiple reasons, but lack of fluid availability is a critical factor, and the survival is not only because of their incorporation in a strong host phase but because of the ability of the host to prevent fluid infiltration until fracturing occurs at low temperatures. High-precision field structural geology mapping in the Yangkou area has revealed the complex deformation history including multi-stage folding events. The earliest folding event occurred before the eclogite reached peak metamorphism, and is preserved as rootless F1 isoclines that preserve the earliest evidence for UHP metamorphism, including intragranular coesite. We report the structural and petrological phenomenon that the intragranular coesite is uniquely preserved within the hinge zones of F1 rootless eclogite folds that have a mineral assemblage of Grt+Omp+Rt+Cs. However, the limbs of F1 folds or overprinted F1+F2 folds have a mineral assemblage of Grt+Omp+Rt+Qtz+Phg, and experienced different degrees of retrogression. The peak metamorphic P-T condition for coesite-bearing eclogite is P=4.0-4.5GPa, 745-909°C. however, the peak metamorphic P-T condition for phengite-quartz bearing eclogite is 3.8-4.1GPa, 733-840°C. The hydrogen concentration was investigated by FTIR (Fourier Transform Infrared Spectroscopy) in these two samples. In the intragranular coesite eclogite, coesite is basically free of water (<10 ppm), very low in garnet (8-50 ppm) and average hydrogen concentration of omphacite is 106-200 ppm; however, with the appearance of phengite and coesite's transformation into quartz, the water content within phengite bearing eclogite is raised. The average hydrogen concentration of garnet is 26-157 ppm , that of omphacite is 270-405 ppm. This indicates that with the appearance of phengite and retrogression, the water content of eclogite is raised up gradually, but at this stage, the eclogite is still within a localized "dry" environment compared to most water-rich (1000-2000ppm) eclogite in the Dabie-Sulu orogen. Through the structural and petrological analysis, we find that the intragranular coesite is more likely preserved within the F1 rootless isoclinal folds which formed prior to the peak metamorphism. This suggests that F1 rootless folds act as rigid and impervious shells under ultrahigh-pressure conditions, and shelter the eclogite from the surrounding fluid, which is helpful to maintain a relatively dry environment during rapid exhumation of UHP rocks, allowing the intergranular coesite to be preserved. This mechanism may have important implications for understanding the prograde path of continental-continental collision, and understanding the structural setting of the preserved intergranular coesite, which has important implications for the search for the early fabrics and metamorphic assemblages in other UHP-terrains around the world.
Kinetics of the coesite to quartz transformation
Mosenfelder, J.L.; Bohlen, S.R.
1997-01-01
The survival of coesite in ultrahigh-pressure (UHP) rocks has important implications for the exhumation of subducted crustal rocks. We have conducted experiments to study the mechanism and rate of the coesite ??? quartz transformation using polycrystalline coesite aggregates, fabricated by devitrifying silica glass cylinders containing 2850H/106 Si at 1000??C and 3.6 GPa for 24h. Conditions were adjusted following synthesis to transform the samples at 700-1000??C at pressures 190-410 MPa below the quartz-coesite equilibrium boundary. Reaction proceeds via grain-boundary nucleation and interface-controlled growth, with characteristic reaction textures remarkably similar to those seen in natural UHP rocks. We infer that the experimental reaction mechanism is identical to that in nature, a prerequisite for reliable extrapolation of the rate data. Growth rates obtained by direct measurement differ by up to two orders of magnitude from those estimated by fitting a rate equation to the transformation-time data. Fitting the rates to Turnbull's equation for growth therefore yields two distinct sets of parameters with similar activation energies (242 or 269 kJ/mol) but significantly different pre-exponential constants. Extrapolation based on either set of growth rates suggests that coesite should not be preserved on geologic time scales if it reaches the quartz stability field at temperatures above 375-400??C. The survival of coesite has previously been linked to its inclusion in strong phases, such as garnet, that can sustain a high internal pressure during decompression. Other factors that may play a crucial role in preservation are low fluid availability - possibly even less than that of our nominally "dry" experiments - and the development of transformation stress, which inhibits nucleation and growth. These issues are discussed in the context of our experiments as well as recent observations from natural rocks. ?? 1997 Elsevier Science B.V.
Liang, Zhili; Mohanty, Paritosh; Fei, Yingwei; Landskron, Kai
2010-12-14
Coesite nanocrystals have been synthesized from periodic mesoporous organosilica (PMO) with (CH(2))(2) bridges heated at 300 °C for 150 min and 12 GPa. The crystals are not sintered, single crystalline, and have diameters of ca. 100-300 nm. Below 300 °C, an amorphous non-porous organosilica glass was obtained. Heating above 300 °C at 12 GPa results in the rapid crystal growth and micron size coesite crystals were formed.
NASA Astrophysics Data System (ADS)
Schulze, D. J.; Page, Z.; Harte, B.; Valley, J.; Channer, D.; Jaques, L.
2006-12-01
Using ion microprobes and secondary-ion mass spectrometry we have analyzed the carbon and oxygen isotopic composition of eclogite-suite diamonds and their coesite inclusions, respectively, from three suites of diamonds of Proterozoic age. Extremely high (for the mantle) oxygen isotope values (delta 18O of +10.2 to +16.9 per mil VSMOW) are preserved in coesites included in eclogitic diamonds from Guaniamo, Venezuela (Schulze et al., Nature, 2003), providing compelling evidence for an origin of their eclogite hosts by subduction of sea water altered ocean floor basalts. In situ SIMS analyses of their host diamonds yield carbon isotope values (delta 13C) of -12 to -18 per mil PDB. SIMS analyses of coesite inclusions from Argyle, Australia diamonds previously analyzed by combustion methods for d13C composition (Jaques et al., Proc. 4th Kimb. Conf, 1989), also yield anomalously high d18O values (+6.8 to +16.0 per mil VSMOW), that correlate with the anomalously low carbon isotope values (-10.3 to -14.1 per mil PDB). One coesite-bearing diamond from Orapa, Botswana analyzed in situ by SIMS has a d18O value of the coesite of +8.5 per mil VSMOW and a d13C value of the adjacent diamond host of -9.0 per mil PDB. A second Orapa stone has a SIMS carbon isotope compositional range of d13C = -14 to -16 per mil PDB, but the coesite is too small for ion probe analysis. At each of these localities, carbon isotope values of coesite-bearing diamonds that are lower than typical of mantle carbon are correlated with oxygen isotope compositions of included coesites that are substantially above the common mantle oxygen isotope range. Such results are not in accord with diamond genesis models involving formation of eclogitic diamonds from igneous melts undergoing fractionation in the mantle or by crystallization from primordial inhomogeneities in Earth's mantle. By analogy with the oxygen isotope compositions of altered ocean floor basalts and Alpine (subduction zone) eclogites they are, however, consistent with a subduction origin for these eclogite assemblages from altered ocean floor basaltic protoliths, and thus the simplest explanation for the source of the low carbon isotope values of these diamonds is formation from biogenic carbon accumulated on or near the ocean floor and subducted to the depths of eclogite and diamond stability with the altered basalts. Significantly these results, which were not predicted from studies of diamond-bearing eclogites, apply to the mantle beneath three different continental crustal blocks of both Proterozoic (Guaniamo and Argyle) and Archean/Proterozoic (Orapa) age.
NASA Astrophysics Data System (ADS)
Knapp, Nadia; Woodland, Alan B.; Klimm, Kevin
2015-07-01
We have experimentally tested the possibility that the coesite-stishovite transition in eclogite bodies is responsible for the X discontinuity, a locally observed, low-impedance jump in seismic wave velocities at 260-330 km depth. We determined phase relations and free SiO2 abundances in three natural-analog eclogite compositions that simulate different subduction scenarios in terms of pressure-temperature conditions and whether or not melt extraction occurred. Eclogitic compositions representing residues after either shallow or deep melting contain either no coesite or else too little (<4 wt %) to produce the observed impedance contrast for the X discontinuity. Only an unmodified mid-ocean ridge basalt (MORB) composition was found to contain just enough coesite (6-8 wt %) to be consistent with the expected impedance contrast when it transforms to stishovite. However, we assert that MORB cannot remain compositionally unmodified during subduction down to ~300 km. Fluid loss due to dehydration reactions during the transformation from basalt to eclogite lowers bulk SiO2 content. In addition, the MORB wet solidus intersects the coesite-stishovite boundary at ~290 km, implying that at greater depths a melt phase should be present before stishovite stability is reached. Our data indicate that melt generation is an efficient means of lowering the free SiO2 content in the mineral assemblage. This study also confirms previous work indicating that exsolution of SiO2 from the Ca-Eskola (Ca0.5AlSi2O6) component in clinopyroxene is not a feasible mechanism for producing significant stishovite upon reaching its stability field. We conclude that the coesite-stishovite transition in eclogite bodies is not a viable petrological explanation for the X discontinuity.
NASA Astrophysics Data System (ADS)
Liou, J. G.; Zhang, R. Y.; Jahn, Bor-ming
1997-08-01
In the Dabie ultrahigh-pressure terrane of east-central China, coesite-bearing jadeite quartzites occur locally as intercalated layers with marble and mafic eclogite. This rock assemblage is, in turn, enclosed within quartzofeldspathic gneisses. Metamorphic parageneses and kelyphitic textures reveal a multistage metamorphic evolution and complex exhumation history. The primary peak metamorphic assemblage consists of jadeite + garnet + coesite + rutile ± apatite. Minor coesite and coesite pseudomorphs occur as inclusions in jadeite and garnet. Three stages of retrograde assemblages are observed in the jadeite quartzites. Stage A is represented by the polymorphic transformation of coesite to quartz aggregates. Stage B is characterized by formation of coronas around jadeite porphyroblasts consisting of an inner layer of oligoclase + amphibole and an outer layer of albite ± aegirine—augite. The last stage (stage C) involved total replacement of jadeite and most garnets by taramitic amphibole + albite + aegirine-augite. Peak metamorphic P-T conditions were > 26 kbar at 660°C and are consistent with the estimates from the adjacent coesite-bearing eclogites. The jadeite quartzites display clockwise P-T path that matches those of the adjacent eclogites. Major and trace element data suggest that the protolith of the jadeite quartzite could have been an albitized siltstone enriched in Na and depleted in K and Ca. The highly negative present-day ɛNd value (-24.7) indicates a very old age for the protolith. Its late Archean model age (TDM) of 2.58 Ga is among the oldest so far identified for rocks from the Dabie UHPM terrane. Concordant field relations and petrogenetic considerations suggest that all mafic, politic, carbonate and gneissic rocks have experienced in-situ UHP metamorphism during Triassic continental collision between the Sino-Korean and Yangtze cratons.
First natural occurrence of coesite
Chao, E.C.T.; Shoemaker, E.M.; Madsen, B.M.
1960-01-01
Coesite, the high-pressure polymorph of SiO2, hitherto known only as a synthetic compound, is identified as an abundant mineral in sheared Coconino sandstone at Meteor Crater, Arizona. This natural occurrence has important bearing on the recognition of meteorite impact craters in quartz-bearing geologic formations.
Multiple pathways in pressure-induced phase transition of coesite
NASA Astrophysics Data System (ADS)
Liu, Wei; Wu, Xuebang; Liang, Yunfeng; Liu, Changsong; Miranda, Caetano R.; Scandolo, Sandro
2017-12-01
High-pressure single-crystal X-ray diffraction method with precise control of hydrostatic conditions, typically with helium or neon as the pressure-transmitting medium, has significantly changed our view on what happens with low-density silica phases under pressure. Coesite is a prototype material for pressure-induced amorphization. However, it was found to transform into a high-pressure octahedral (HPO) phase, or coesite-II and coesite-III. Given that the pressure is believed to be hydrostatic in two recent experiments, the different transformation pathways are striking. Based on molecular dynamic simulations with an ab initio parameterized potential, we reproduced all of the above experiments in three transformation pathways, including the one leading to an HPO phase. This octahedral phase has an oxygen hcp sublattice featuring 2 × 2 zigzag octahedral edge-sharing chains, however with some broken points (i.e., point defects). It transforms into α-PbO2 phase when it is relaxed under further compression. We show that the HPO phase forms through a continuous rearrangement of the oxygen sublattice toward hcp arrangement. The high-pressure amorphous phases can be described by an fcc and hcp sublattice mixture.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Trukhin, A. N., E-mail: truhins@cfi.lu.lv
2014-10-21
Stishovite, coesite, oxygen deficient silica glass as well as irradiated α-quartz, exhibit two luminescence bands: a blue one and an UV one both excitable in the range within optical gap. There are similarities in spectral position and in luminescence decay kinetics among centers in these materials. The interpretation was done on the model of Oxygen Deficient Centers (ODC) [1]. The ODC(II) or twofold coordinated silicon and ODC(I) are distinguished. ODC(I) is object of controversial interpretation. The Si-Si oxygen vacancy [2] and complex defect including latent twofold coordinated silicon [3] are proposed. Remarkably, this luminescence center does not exist in asmore » grown crystalline α-quartz. However, destructive irradiation of α-quartz crystals with fast neutrons, γ rays, or dense electron beams [4–6] creates ODC(I) like defect. In tetrahedron structured coesite the self trapped exciton (STE) luminescence observed with high energetic yield (∼30%) like in α-quartz crystals. STE in coesite coexists with oxygen deficient-like center. In octahedron structured stishovite STE was not found and only ODC exists.« less
NASA Astrophysics Data System (ADS)
Chen, Ting; Liebermann, Robert C.; Zou, Yongtao; Li, Ying; Qi, Xintong; Li, Baosheng
2017-08-01
The compressional and shear wave velocities for coesite have been measured simultaneously up to 5.8 GPa and 1073 K by ultrasonic interferometry for the first time. The shear wave velocity decreases with pressure along all isotherms. The resulting contrasts between coesite and stishovite reach 34% and 45% for
DOE Office of Scientific and Technical Information (OSTI.GOV)
Chen, Ting; Liebermann, Robert C.; Zou, Yongtao
The compressional and shear wave velocities for coesite have been measured simultaneously up to 5.8 GPa and 1073 K by ultrasonic interferometry for the first time. The shear wave velocity decreases with pressure along all isotherms. The resulting contrasts between coesite and stishovite reach ~34% and ~45% for P and S wave velocities, respectively, and ~64% and ~75% for their impedance at mantle conditions. The large velocity and impedance contrasts across coesite-stishovite transition imply that to generate the velocity and impedance contrasts observed at the X-discontinuity, only a small amount of silica would be required. The velocity jump dependences onmore » silica, d(lnVP)/d(SiO2) = 0.38 (wt %)-1 and d(lnVS)/d(SiO2) = 0.52 (wt %)-1, are utilized to place constraints on the amount of silica in the upper mantle and provide a geophysical approach to track mantle eclogite materials and ancient subducted oceanic slabs.« less
Multiple pathways in pressure-induced phase transition of coesite
Liu, Wei; Wu, Xuebang; Liu, Changsong; Miranda, Caetano R.; Scandolo, Sandro
2017-01-01
High-pressure single-crystal X-ray diffraction method with precise control of hydrostatic conditions, typically with helium or neon as the pressure-transmitting medium, has significantly changed our view on what happens with low-density silica phases under pressure. Coesite is a prototype material for pressure-induced amorphization. However, it was found to transform into a high-pressure octahedral (HPO) phase, or coesite-II and coesite-III. Given that the pressure is believed to be hydrostatic in two recent experiments, the different transformation pathways are striking. Based on molecular dynamic simulations with an ab initio parameterized potential, we reproduced all of the above experiments in three transformation pathways, including the one leading to an HPO phase. This octahedral phase has an oxygen hcp sublattice featuring 2 × 2 zigzag octahedral edge-sharing chains, however with some broken points (i.e., point defects). It transforms into α-PbO2 phase when it is relaxed under further compression. We show that the HPO phase forms through a continuous rearrangement of the oxygen sublattice toward hcp arrangement. The high-pressure amorphous phases can be described by an fcc and hcp sublattice mixture. PMID:29162690
Coesite inclusions in diamonds of Yakutia
NASA Astrophysics Data System (ADS)
Bardukhinov, L. D.; Spetsius, Z. V.; Monkhorov, R. V.
2016-10-01
The results of the study of diamonds with inclusions of high-pressure modification of SiO2 (coesite) by Raman spectroscopy are reported. It is established that the octahedral crystal from the Zapolyarnaya pipe is characterized by the highest residual pressure (2.7 ± 0.07 GPa). An intermediate value of this parameter (2.1 ± 0.07 GPa) was obtained for a crystal of transitional habit from the Maiskaya pipe. The minimal Raman shift was registered for coesite in diamond from the Komsomol'skaya-Magnitnaya pipe and provided a calculated residual pressure of 1.8 ± 0.03 GPa. The residual pressures for crystals from the placer deposits of the Kuoika and Bol'shaya Kuonamka rivers are 2.7 ± 0.07 and 3.1 ± 0.1 GPa, respectively. Octahedral crystals were formed in the mantle at a higher pressure than rhombododecahedral diamonds.
High-pressure infrared sepctra of alpha-quartz, coesite, stishovite and silica glass
NASA Technical Reports Server (NTRS)
Williams, Q.; Hemley, R. J.; Kruger, M. B.; Jeanloz, R.
1993-01-01
High-pressure infrared absorption spectra of alpha-quatz, coesite, stishovite, and SiO2 glass are consistent with the primary compression mechanism of the initially tetrahedrally bonded phases being the bending of the Si-O-Si angle at pressures less than 10-20 GPa. At higher pressures, up to 40 GPa, we observe a decline in the intensity of the infrared SiO4 asymmetric-stretching vibrations of all three phases, with an increase in the relative amplitude between 700 and 900/cm. This change in intensities is attributed to an increase in the average coordination number of silicon through extreme distortion of tetrahedra. At pressures above approximately 20 GPa, the low-pressure crystalline polymorphs gradually become amorphous, and the infrared spectra provide evidence for an increase in silicon coordination in these high-density amorphous phases. The pressure-amorphized samples prepared from quartz and coesite differ structurally both from each other and from silica glass that has been compressed, and the high pressure spectra indicate that these materials are considerably more disordered than stishovite under comparable pressure conditions. Average mode Grueneisen parameters calculated for quartz, stishovite and fused silica from both infrared and Raman spectra are compatible with the corresponding thermodynamic value of the Grueneisen parameter, however, that of coesite is significantly discrepant.
NASA Astrophysics Data System (ADS)
Spray, John G.; Boonsue, Suporn
2018-01-01
Coesite and stishovite are developed in shock veins within metaquartzites beyond a radius of 30 km from the center of the 2.02 Ga Vredefort impact structure. This work focuses on deploying analytical field emission scanning electron microscopy, electron backscattered diffraction, and Raman spectrometry to better understand the temporal and spatial relations of these silica polymorphs. α-Quartz in the host metaquartzites, away from shock veins, exhibits planar features, Brazil twins, and decorated planar deformation features, indicating a primary (bulk) shock loading of >5 < 35 GPa. Within the shock veins, coesite forms anhedral grains, ranging in size from 0.5 to 4 μm, with an average of 1.25 μm. It occurs in clasts, where it displays a distinct jigsaw texture, indicative of partial reversion to a less dense SiO2 phase, now represented by microcrystalline quartz. It is also developed in the matrix of the shock veins, where it is typically of smaller size (<1 μm). Stishovite occurs as euhedral acicular crystals, typically <0.5 μm wide and up to 15 μm in length, associated with clast-matrix or shock vein margin-matrix interfaces. In this context, the needles occur as radiating or subparallel clusters, which grow into/over both coesite and what is now microcrystalline quartz. Stishovite also occurs as more blebby, subhedral to anhedral grains in the vein matrix (typically <1 μm). We propose a model for the evolution of the veins (1) precursory frictional melting in a microfault ( 1 mm wide) generates a molten matrix containing quartz clasts. This is followed by (2) arrival of the main shock front, which shocks to 35 GPa. This generates coesite in the clasts and in the matrix. (3) On initial shock release, the coesite partly reverts to a less dense SiO2 phase, which is now represented by microcrystalline quartz. (4) With continued release, stishovite forms euhedral needle clusters at solid-liquid interfaces and as anhedral crystals in the matrix. (5) With decreasing pressure-temperature, the matrix completes crystallization to yield a microcrystalline quasi-igneous texture comprising quartz-coesite-stishovite-kyanite-biotite-alkali feldspar and accessory phases. It is possible that the shock vein represents the locus of a thermal spike within the bulk shock, in which case there is no requirement for additional pressure (i.e., the bulk shock was ≃35 GPa). However, if that pressure was not realized from the main shock, then supplementary pressure excursions within the vein would have been required. These could have taken the form of localized reverberations from wave trapping, or implosion processes, including pore collapse, phase change-initiated volume reduction, and melt cavitation.
NASA Astrophysics Data System (ADS)
Fauconnier, J.; Gasc, J.; Petit, L.; Pinquier, Y.; Deldicque, D.; Renner, J.; Green, H. W., II; Schubnel, A.
2017-12-01
A new high pressure Griggs-type apparatus, equipped with ultrasonic transducers, was developed at the École Normale Supérieure (France). This press uses solid salt as confining medium and can reach 5 GPa confinement within a 20 mm borehole. Two piezoelectric transducers, with 5MHz center frequency, are installed above and below the sample, respectively in the deformation column and in the base plate. During the experiment, the top and bottom transducers are used as ultrasonic source and receiver, respectively, for pulse-through measurements. Full waveforms are digitized at 50MHz, and relative elastic waves travel times through the sample and part of the deformation column are calculated using cross-correlations.In order to calibrate our acoustic system, an alumina dummy was used to estimate the sensitivity of the setup (i.e. the minimum travel time difference between two measurements) and the acoustic `stiffness' of the apparatus (i.e. the relative change of travel time as a function of pressure, temperature and differential stress). We show that our resolution in relative travel time change is of the order of 10 ns, meaning that within a 7 mm long sample and given an average wave velocity of mineral assemblies of the order of 6-10 km/s, our theoretical resolution in velocity change in the sample is close to 1%.The aim of a second set of experiments is to study the kinetics of the quartz-coesite reaction under non-hydrostatic conditions. At our (P,T) conditions, P-wave velocities in coesite are roughly 25 % higher than in (metastable) quartz. Experiments were performed on 10-20 µm quartz powder, at 800°C and confining pressures ranging from 1 to 3 GPa. During each experiment, the maximum principal stress, σ1, was raised within the coesite field, at fixed σ3 and temperature conditions. Stress and temperature were then kept constant during 2 hours. Microstructures and phases distribution were characterized post-mortem using EBSD mapping. Preliminary results reveal that coesite was only observed when both σ3 and σ1 were in the coesite field. In this case, using our ultrasonic monitoring, the reaction was detected by a clear change of P-wave velocity in the sample, as approximately 20% of the quartz transformed to coesite.
Thermal expansion of coesite determined by synchrotron powder X-ray diffraction
NASA Astrophysics Data System (ADS)
Kulik, Eleonora; Murzin, Vadim; Kawaguchi, Shogo; Nishiyama, Norimasa; Katsura, Tomoo
2018-05-01
Thermal expansion of synthetic coesite was studied with synchrotron powder X-ray diffraction in the temperature range of 100-1000 K. We determined the unit cell parameters of monoclinic coesite (a, b, c, and β) every 50 K in this temperature range. We observed that a and b parameters increase with increasing temperature, while c decreases. The β angle also decreases with temperature and approaches 120°. As a result, the unit cell volume expands by only 0.7% in this temperature range. Our measurements provide thermal expansion coefficients of coesite as a function of temperature: it increases from 3.4 × 10-6 K-1 at 100 K to 9.3 × 10-6 K-1 at 600 K and remains nearly constant above this temperature. The Suzuki model based on the zero-pressure Mie-Grüneisen equation of state was implemented to fit the unit cell volume data. The refined parameters are {V_0} = 546.30(2) Å3, Q = 7.20(12) × 106 J/mol and {θ D} = 1018(43) K, where {θ D} is the Debye temperature and {V_0} is the unit cell volume at 0 K with an assumption that {K^' } is equal to 1.8. The obtained Debye temperature is consistent with that determined in a previous study for heat capacity measurements.
Ionic network analysis of tectosilicates: the example of coesite at variable pressure.
Reifenberg, Melina; Thomas, Noel W
2018-04-01
The method of ionic network analysis [Thomas (2017). Acta Cryst. B73, 74-86] is extended to tectosilicates through the example of coesite, the high-pressure polymorph of SiO 2 . The structural refinements of Černok et al. [Z. Kristallogr. (2014), 229, 761-773] are taken as the starting point for applying the method. Its purpose is to predict the unit-cell parameters and atomic coordinates at (p-T-X) values in-between those of diffraction experiments. The essential development step for tectosilicates is to define a pseudocubic parameterization of the O 4 cages of the SiO 4 tetrahedra. The six parameters a PC , b PC , c PC , α PC , β PC and γ PC allow a full quantification of the tetrahedral structure, i.e. distortion and enclosed volume. Structural predictions for coesite require that two separate quasi-planar networks are defined, one for the silicon ions and the other for the O 4 cage midpoints. A set of parametric curves is used to describe the evolution with pressure of these networks and the pseudocubic parameters. These are derived by fitting to the crystallographic data. Application of the method to monoclinic feldspars and to quartz and cristobalite is discussed. Further, a novel two-parameter quantification of the degree of tetrahedral distortion is described. At pressures in excess of ca 20.45 GPa it is not possible to find a self-consistent solution to the parametric curves for coesite, pointing to the likelihood of a phase transition.
NASA Astrophysics Data System (ADS)
Mueller, H. J.; Schilling, F. R.; Lauterjung, J.; Lathe, C.
2001-12-01
The high pressure SiO2-polymorph coesite seems to be an important mineral in the subduction process including crustal material (Chopin, 1984; Schreyer, 1995). The quartz to coesite transition is thus of fundamental importance to understand the processes within a subducting crust. Furthermore, the nature of the quartz to coesite transition is discussed controversially, because high pressure XRD-studies suggest an intermediate phase during the transformation process (Zinn et al., 1997). For the combined determination of elastic properties and structure a cubic multi-anvil high pressure apparatus (MAX80) was used. For the maximum sample volume of 20 mm3 the pressure limit is about 7GPa. The pressure is measured by use of NaCl as an internal pressure marker with calibrated PVT-data. The maximum temperature of about 2,000K is generated by an internal graphite heater and controlled by a thermocouple. The synchrotron beam (100x100 microns) is guided by a collimator through the sample between the anvils. For energy-dispersive X-ray diffraction, a Ge-solid state detector analyses the diffracted white beam at a fixed angle. The compressional and shear wave velocities were determined simultaneously by ultrasonic interferometry inside MAX80. Two of the six anvils are equipped with overtone polished lithium niobate transducers at their rear side, outside the volume under pressure, for generation and detection of ultrasonic waves between 10 and 60 MHz. Different buffer - reflector combinations and transducer arrangements were used to optimize the critical interference between both sample echoes. Therefore MAX80 is equipped for asymmetrical and symmetrical interferometric set-ups, i.e. compressional and shear waves are generated from the same or from two anvils, opposite to each other. We used for our transient measurements 3 natural fine-grained quartzites from Turkey and Germany. As a first step the pressure was increased gradually up to 4GPa at ambient temperature. At each pressure Vp and Vs was measured by ultrasonic interferometry. After reaching a given pressure, temperature was increased. At 4.5GPa and 800\\deg C the phase transition to coesite took place in less than 2 minutes. The fast kinetic of transformation was observed by synchrotron radiation. The compressional wave velocity increased by 30% and the shear wave velocity by 10% during the phase transition. The kinetic of the transition was varied by choosing different pressure and temperature conditions. The transformation with lower kinetic was studied in detail by XRD and ultrasonic interferometry. At 4.2 GPa the transformation could not be observed even above 950\\deg C. At 4.5 GPa and 750\\deg C the transition stopped at about 50% transformation, but transforms complete while increasing temperature to 800\\deg C. After the phase transition monitored by X-ray scattering the sample was quenched and Vp and Vs of coesite was measured at ambient temperatures up to the maximum pressure. Small differences in grain size, shape and in minor graphite contents did not change systematically the PT-conditions and kinetics. In addition to the kinetic and change of elastic properties the pressure and temperature derivatives of elastic properties of coesite will be presented.\\Chopin, C., Contr. Min. Petrol., 86 (1984), 107-118\\Schreyer, W., J. Geophys. Res., 100 (1995), 8,353-8,366\\Zinn P., Lauterjung J., Wirth R. & Hinze E. Zeitschrift für Kristallographie, 212 (1997), 691-698.
McClelland, W.C.; Power, S.E.; Gilotti, J.A.; Mazdab, F.K.; Wopenka, B.
2006-01-01
Obtaining reliable estimates for the timing of eclogite-facies metamorphism is critical to establishing models for the formation and exhumation of high-pressure and ultrahigh-pressure (UHP) metamorphic terranes in collisional orogens. The presence of pressure-dependent phases, such as coesite, included in metamorphic zircon is generally regarded as evidence that zircon growth occurred at UHP conditions and, ifdated, should provide the necessary timing information. We report U-Pb sensitive high-resolution ion microprobe (SHRIMP) ages and trace-element SHRIMP data from coesite-bearing zircon suites formed during UHP metamorphism in the North- East Greenland Caledonides. Kyanite eclogite and quartzofeldspathic host gneiss samples from an island in J??kelbugt (78??00'N, 18??04'W) contained subspherical zircons with well-defined domains in cathodoluminescence (CL) images. The presence of coesite is confirmed by Raman spectroscopy in six zircons from four samples. Additional components of the eclogite-facies inclusion suite include kyanite, omphacite, garnet, and rutile. The trace-element signatures in core domains reflect modification of igneous protolith zircon. Rim signatures show flat heavy rare earth element (HREE) patterns that are characteristic of eclogite-facies zircon. The kyanite eclogites generally lack a Eu anomaly, whereas a negative Eu anomaly persists in all domains of the host gneiss. The 207Pb- corrected 206Pb/238U ages range from 330 to 390 Ma for the host gneiss and 330-370 Ma for the kyanite eclogite. Weighted mean 206Pb/238U ages for coesite-bearing domains vary from 364 ?? 8 Ma for the host gneiss to 350 ?? 4 Ma for kyanite eclogite. The combined U-Pb and REE data interpreted in conjunction with observed CL domains and inclusion suites suggest that (1) Caledonian metamorphic zircon formed by both new zircon growth and recrystallization, (2) UHP metamorphism occurred near the end of the Caledonian collision, and (3) the 30-50m.y. span of ages records long residence times at eclogite-facies conditions for the UHProcks of North-East Greenland. This spread in observed ages is interpreted to be characteristic of metamorphic rocks that have experienced relatively long (longer than 10 m.y.) residence times at UHP conditions. ?? 2006 Geological Society of America.
Crystallization of biogenic hydrous amorphous silica
NASA Astrophysics Data System (ADS)
Kyono, A.; Yokooji, M.; Chiba, T.; Tamura, T.; Tuji, A.
2017-12-01
Diatom, Nitzschia cf. frustulum, collected from Lake Yogo, Siga prefecture, Japan was cultured in laboratory. Organic components of the diatom cell were removed by washing with acetone and sodium hypochlorite. The remaining frustules were studied by SEM-EDX, FTIR spectroscopy, and synchrotron X-ray diffraction. The results showed that the spindle-shaped morphology of diatom frustule was composed of hydrous amorphous silica. Pressure induced phase transformation of the diatom frustule was investigated by in situ Raman spectroscopic analysis. With exposure to 0.3 GPa at 100 oC, Raman band corresponding to quartz occurred at ν = 465 cm-1. In addition, Raman bands known as a characteristic Raman pattern of moganite was also observed at 501 cm-1. From the integral ratio of Raman bands, the moganite content in the probed area was estimated to be approximately 50 wt%. With the pressure and temperature effect, the initial morphology of diatom frustule was completely lost and totally changed to a characteristic spherical particle with a diameter of about 2 mm. With keeping the compression of 5.7 GPa at 100 oC, a Raman band assignable to coesite appeared at 538 cm-1. That is, with the compression and heating, the hydrous amorphous silica can be readily crystallized into quartz, moganite, and coesite. The first-principles calculations revealed that a disiloxane molecule stabilized in a trans configuration is twisted 60o and changed into the cis configuration with a close approach of water molecule. It is therefore a reasonable assumption that during crystallization of hydrous amorphous silica, the Si-O-Si bridging unit with the cis configuration would survive as a structural defect and then crystallized into moganite by keeping the geometry. This hypothesis is adaptable to the phase transformation from hydrous amorphous silica to coesite as well, because coesite has the four-membered rings and easily formed from the hydrous amorphous silica under high pressure and high temperature conditions.
Discovery of coesite and shocked quartz associated with the upper Eocene cpx spherule layer
NASA Technical Reports Server (NTRS)
Liu, S.; Kyte, T.; Glass, B. P.
2002-01-01
At least two major impact ejecta layers have been discovered in upper Eocene strata. The upper layer is the North American microtektite layer. lt consists tektite fragments, microtektites, and shocked mineral grains (e.g., quartz and feldspar with multiple sets of PDFs, coesite and reidite (a high-pressure polymorph of zircon)). The slightly older layer contains clinopyroxene-bearing (cpx) spherules and microtektites associated with an Ir anomaly. The North American tektite layer may be derived from the Chesapeake Bay impact structure, and the cpx spherule layer may from the Popigai impact crater. A cpx spherule layer associated with a positive Ir anomaly was recently found at ODP Site 709, western Indian Ocean. A large sample (Hole 709C, core 31, section 4, 145-150 cm), originally used for a study of interstitial water by shipboard scientists, was acquired for the purpose of recovering a large number of spherules for various petrographic and geochemical studies. A split of the sample (50.35 g) was disaggregated and wet-sieved. More than 17,000 cpx spherules and several hundred microtektites (larger than 125 microns) were recovered from the sample. Rare white opaque grains were observed in the 125-250 micron size fraction after removal of the carbonate component using dilute HCI. Seven of the white opaque grains were X-rayed using a Gandolfi camera and six were found to be coesite (probably mixed with lechatelierite). Eighty translucent colorless grains from the 63-125 micron size fraction were studied with a petrographic microscope. Four of the grains exhibit one to two sets of planar deformation features (PDFs). The only other possible known occurrence of shocked minerals associated with the cpx spherule layer is at Massignano, Italy, where pancake-shaped clay spherules (thought to be diagenetically altered cpx spherules are associated with a positive Ir anomaly and Ni- rich spinel crystals. Shocked quartz grains with multiple sets of PDFs also occur at this site. Until now, unmelted impact ejecta have not been found associated with the cpx spherules at any of the other 20 sites around the world and this is the first time that coesite has been found associated with the cpx spherule layer. The discovery of coesite and shocked quartz associated with the cpx spherules at Site 709 in Indian Ocean is further evidence for the impact origin of the cpx spherule layer. We hope that future discovery of other unmelted minerals from this sample may provide materials to establish constraints on the provenance of this late Eocene ejecta.
NASA Astrophysics Data System (ADS)
Schmidt, Max W.; Poli, Stefano
1994-06-01
The breakdown reactions of lawsonite in SiO2 + H2O- and in Al2O3 + H2O-saturated synthetic CASH systems were examined between 17 and 92 kbar in both forward and reversed experiments. Lawsonite is stable to 565 C at 20 kbar, 760 C at 40 kbar, and 980 C at 65 kbar. In this pressure range lawsonite breaks down to zoisite + kyanite + quartz/ coesite + H2O. An invariant point occurs at 1000 C, 67 kbar. At higher pressures lawsonite breaks down to the assemblage grossular + kyanite + coesite + H20. The steep positive dP/dT slope of this higher pressure breakdown reaction becomes steeply negative when coesite transforms to stishovite. At 92 kbar, the highest pressure investigated, lawsonite is stable to 1040 C. The invariant point marks also the pressure stability limit of zoisite since zoisite reacts to lawsonite + grossular + kyanite + coesite (at temperatures below 1000 C), to grossular + kyanite + coesite + H2O (1000-1040 C) and to grossular + kyanite + melt + H20 (above 1040C). These three reactions have a flat Clapeyron slope, and they locate the maximum pressure stability of zoisite between 65 and 68 kbar (between 800 and 1200 C). Eutectic melting in the SiO2 + H2O-saturated CASH system occurs for the assemblage zoisite + kyanite + coesite + H2O at temperatures approximately 100 C (at 40 kbar) to 40 C (at 65 kbar) higher than the lawsonite breakdown reaction. In the Al2O3+H2O-saturated system the reaction lawsonite + diaspore/corundum = zoisite + kyanite + H2O limits the stability of lawsonite. The diaspore = corundum + H2O equilibrium is found to be located about 50 C lower than predicted by previous studies. The equilibrium boundaries of the reactions between 17 and 38 kbar from both SiO2+H2O- and Al2O3 + H2O-saturated chemical systems were used to improve the thermochemical data on lawsonite. Two sets of thermodynamic properties internally consistent with the databases of both Berman and Holland and Powell, and also consistent with most previous experimental studies, were calculated employing the technique of linear programming (for Berman's data) and a least-squares fit procedure (for Holland and Powell's data). Because lawsonite is stable to 1040 C at 92 kbar, a temperature far higher than predicted by thermal modelling of subduction zones, it is expected to be stable in metabasalts and intermediate compositions (e.g., andesites and greywackes) subducted to depths exceeding 300 km. Lawsonite contains 11 wt% water in its structure, and is thus capable of transporting water deep into the mantle. Its breakdown would contribute significantly to the fluid budget of the slab and overlying mantle wedge. The experimental data in combination with thermal modelling studies indicate that a complete dehydration of the descending oceanic crust is unlikely to occur at shallow levels.
Friction measurements in piston-cylinder apparatus using quartz-coesite reversible transition
NASA Technical Reports Server (NTRS)
Akella, J.
1979-01-01
The value of friction determined by monitoring piston displacement as a function of nominal pressure on compression and decompression cycles at 1273 K is compared with the friction value obtained by reversing the quartz-coesite transition at 1273 and 1073 K in a talc-glass-alsimag cell (Akella and Kennedy, 1971) and a low-friction salt cell (Mirwald et al., 1975). Quenching runs at 1273 K gave double values of friction of 0.25 GPa for the talc-glass-alsimag cell and 0.03 GPa for the salt cell. The piston-displacement technique gave somewhat higher values. Use of piston-displacement hysteresis loops in evaluating the actual pressure on a sample may lead to overestimates for decompression runs and underestimates for compression runs.
NASA Astrophysics Data System (ADS)
Martini, J. E. J.
1991-04-01
The Vredefort Dome represents the uplift centre of a well known 2.00 Ga old impact structure of unusually large magnitude. Shock features like shatter cones, planar features and high-pressure silica polymorphs are common. The present study deals with the description, mode of occurrence, field distribution and post-shock metamorphic alteration of coesite and stishovite which were poorly documented up to now. These minerals occur as unusually large crystals in the quartzite of the wall rock in contact with very thin pseudotachylite veins. In the pseudotachylite itself, which can be interpreted as a friction and/or a shock recovery melt, fine needles of kyanite are ubiquitous. It is proposed that these thin pseudotachylites (A-type) formed during the transit of the shock wave. They preceded the development of thick pseudotachylite and microbreccia veins (B-type) which formed during the tensional period which immediately followed. From comparison with the model of formation of high-pressure polymorphs in porous sandstone, it is suggested that higher pressure and stress was concentrated along the A-type veins at the arrival of the shock front. At this time the quartz was transformed into a "high-pressure phase" which was probably poorly crystalline. Behind the shock front, that is during the rarefaction, the pressure was progressively released and the polymorphs crystallized from this initial "high-pressure phase". Stishovite crystallized first, followed by coesite. The high-pressure conditions may have lasted an unusually long time due to the magnitude of the Vredefort impact. This long time, probably about one second, may account for the large size of the coesite and stishovite crystals. Most of the high-pressure silica polymorphs are corroded to a variable degree by secondary quartz and preserved only in a restricted area of the impact structure. This alteration is attributed to post-shock metamorphism due to the temperature of the rock before impact plus the heat left after shock recovery. Some of the evidence put forward by authors against the impact model is discussed according to the facts arising from this investigation. It is concluded that an origin by impact remains the simplest and most realistic model to explain the origin of the Vredefort Dome.
NASA Astrophysics Data System (ADS)
Miyahara, Masaaki; Ohtani, Eiji; Yamaguchi, Akira
2017-11-01
An impact event recorded in the Northwest Africa (NWA) 8275 LL7 ordinary chondrite was investigated based on high-pressure mineralogy of pervasive shock-melt veins present in the rock. NWA 8275 consists of olivine, low-Ca pyroxene, plagioclase (albite-oligoclase composition), and minor high-Ca pyroxene, K-feldspar, phosphate minerals, metallic Fe-Ni and iron sulfide. Plagioclase and K-feldspar grains near the shock-melt veins have become amorphous, although no high-pressure polymorphs of olivine and pyroxene were identified in or adjacent the shock-melt veins. Raman spectroscopy and focused ion beam (FIB)-assisted transmission electron microscopy (TEM) observations reveal that plagioclase entrained around the center portion of the shock-melt veins has dissociated into a jadeite + coesite assemblage. Alternately stacked jadeite and coesite crystals occur in the original plagioclase. On approaching the host rock/shock-melt vein, only jadeite is present. Based on the high-pressure polymorph assemblage, the shock pressure and temperature conditions recorded in the shock-melt veins are ∼3-12 GPa and ∼1973-2373 K, respectively. Following a Rankine-Hugoniot relationship, the impact velocity was at least ∼0.45-1.54 km/s. The duration of high-pressure and high-temperature (HPHT) conditions required for the albite dissociation reaction is estimated a maximum of ∼4-5 s using the phase transition rate of albite, implying that a body of up to ∼9-12 km across collided with the parent body of NWA 8275. The coexistence of jadeite and coesite, the latter of which rarely accompanies jadeite in shocked ordinary chondrites, as a dissociation product of albite requires relatively long duration HPHT conditions. Thus, the impact event recorded in NWA 8275 was likely caused by a larger-than-typical projectile.
Proceedings of the Geophysical Laboratory/Lawrence Radiation Laboratory Cratering Symposium
DOE Office of Scientific and Technical Information (OSTI.GOV)
Nordyke, Milo D.
1961-10-01
The geological papers in this morning's session will deal descriptively with surficial features and end products of impact craters caused by meteorite falls. Such items as breccia, structural deformation, normal and inverse stratigraphy, glass (fused rock), and coesite will frequently be mentioned. Meteor and explosion crater data are presented.
Stresses and pressures at the quartz-coesite transition in shear experiments
NASA Astrophysics Data System (ADS)
Richter, B.; Stunitz, H.; Heilbronner, R.
2015-12-01
Experiments on quartz (qtz) gouge were performed in a Griggs-type deformation apparatus at displacement rates of ~1.3 x 10-5 mms-1 or ~1.3 x 10-4 mms-1, at Pc= 1.0 GPa or 1.5 GPa and T = 600°C to 800°C. The starting material is a natural hydrothermally grown single crystal that was crushed to a powder with grain size d < 100 µm. Coesite (coe) is found if the maximum principle stress (σ1) is in the coe stability field. In general Pc and the mean stress (Pm) of these samples are below the quartz-coesite phase transition (QCT). Coe is not found if σ1 is below the QCT. At T = 600 °C, σ1is always in the coe stability field. But coe is only present in the high strain experiment, indicating slow transformation kinetics. In one sample we observed that σ1crosses the QCT during the loading part and after progressive weakening crosses the QCT back into the qtz stability field. The microstructure of this sample shows the formation of coe and the reverse transformation from coe to qtz. The coe growth penetrates the sample and coe grows around and in between larger qtz clasts. At high stresses, where Pm is also above the QCT, coe often forms radiating aggregates. At lower stresses, where only σ1 lies in the stability field of coe, and at low strain the coe grains have a preferred orientation of the b-axes (sub-) parallel to σ1. With increasing strain, the rigid coe grains rotate and align with the preferred qtz fabric. For coe to be found, it is sufficient that σ1 reaches values above the transformation pressure. If σ1 drops back into the qtz stability field during an experiment, a back-reaction from coe to qtz is observed. It appears therefore that the pressure that defines the QCT is not Pc or Pm, but σ1.
Calibrating the Grigg's' Apparatus using Experiments performed at the Quartz-Coesite Transition
NASA Astrophysics Data System (ADS)
Heilbronner, R.; Stunitz, H.; Richter, B.
2015-12-01
The Griggs deformation apparatus is increasingly used for shear experiments. The tested material is placed on a 45° pre-cut between two forcing blocks. During the experiment, the axial displacement, load, temperature, and confining pressure are recorded as a function of time. From these records, stress, strain, and other mechanical data can be calculated - provided the machine is calibrated. Experimentalists are well aware that calibrating a Griggs apparatus is not easy. The stiffness correction accounts for the elastic extension of the rig as load is applied to the sample. An 'area correction' accounts for the decreasing overlap of the forcing blocks as slip along the pre-cut progresses. Other corrections are sometimes used to account for machine specific behaviour. While the rig stiffness can be measured very accurately, the area correction involves model assumptions. Depending on the choice of the model, the calculated stresses may vary by as much as 100 MPa. Also, while the assumptions appear to be theoretically valid, in practice they tend to over-correct the data, yielding strain hardening curves even in cases where constant flow stress or weakening is expected. Using the results of experiments on quartz gouge at the quartz-coesite transition (see Richter et al. this conference), we are now able to improve and constrain our corrections. We introduce an elastic salt correction based on the assumption that the confining pressure is increased as the piston advances and reduces the volume in the confining medium. As the compressibility of salt is low, the correction is significant and increases with strain. Applying this correction, the strain hardening artefact introduced by the area correction can be counter-balanced. Using a combination of area correction and salt correction we can now reproduce strain weakening, for which there is evidence in samples where coesite transforms back to quartz.
Field occurrences and petrology of eclogites from the Dabie Mountains, Anhui, central China
NASA Astrophysics Data System (ADS)
Wang, X.; Jing, Y.; Liou, J. G.; Pan, G.; Liang, W.; Xia, M.; Maruyama, S.
1990-11-01
Four distinct types of eclogites are recognized according to their field occurrences and mineral parageneses in a gneiss terrane of the Dabie Mountains, a collision zone between the Sino-Korean and Yangtze cratons in central China. Some eclogites contain coesite and its quartz pseudomorphs enclosed in garnet and omphacite. Type I eclogites occur as layers in serpentinites and contain garnet, clinopyroxene, orthopyroxene, phengite, rutile, and coesite pseudomorph. Type II eclogites occur as lenticular bodies inside serpentinites and contain garnet, clinopyroxene, quartz, rutile, and edenitic hornblende. Type III eclogites occur as blocks of 2 cm to 20 m in size in a matrix of hornblende gneiss and biotite gneiss, and Type IV eclogites occur as thin layers interbedded with amphibolites. P- T estimates for these different eclogites indicate that they were formed under different physical conditions. All the eclogites were affected by later regional metamorphism for which the P- T conditions are estimated. This paper provides an introduction to the abundant eclogites from central China which have not been reported previously in Western literature. Specifically, the mode of field occurrence, petrography, mineral chemistry and formation conditions of the four types of eclogites are described. The paper is thus designed to establish a petrological framework for future detailed studies of the eclogites and their country rocks in an ancient zone of collision.
NASA Astrophysics Data System (ADS)
Carl, Eva-Regine; Mansfeld, Ulrich; Liermann, Hanns-Peter; Danilewsky, Andreas; Langenhorst, Falko; Ehm, Lars; Trullenque, Ghislain; Kenkmann, Thomas
2017-07-01
Hypervelocity collisions of solid bodies occur frequently in the solar system and affect rocks by shock waves and dynamic loading. A range of shock metamorphic effects and high-pressure polymorphs in rock-forming minerals are known from meteorites and terrestrial impact craters. Here, we investigate the formation of high-pressure polymorphs of α-quartz under dynamic and nonhydrostatic conditions and compare these disequilibrium states with those predicted by phase diagrams derived from static experiments under equilibrium conditions. We create highly dynamic conditions utilizing a mDAC and study the phase transformations in α-quartz in situ by synchrotron powder X-ray diffraction. Phase transitions of α-quartz are studied at pressures up to 66.1 and different loading rates. At compression rates between 0.14 and 1.96 GPa s-1, experiments reveal that α-quartz is amorphized and partially converted to stishovite between 20.7 GPa and 28.0 GPa. Therefore, coesite is not formed as would be expected from equilibrium conditions. With the increasing compression rate, a slight increase in the transition pressure occurs. The experiments show that dynamic compression causes an instantaneous formation of structures consisting only of SiO6 octahedra rather than the rearrangement of the SiO4 tetrahedra to form a coesite. Although shock compression rates are orders of magnitude faster, a similar mechanism could operate in impact events.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Carl, Eva-Regine; Mansfeld, Ulrich; Liermann, Hanns-Peter
Hypervelocity collisions of solid bodies occur frequently in the solar system and affect rocks by shock waves and dynamic loading. A range of shock metamorphic effects and high-pressure polymorphs in rock-forming minerals are known from meteorites and terrestrial impact craters. In this paper, we investigate the formation of high-pressure polymorphs of α-quartz under dynamic and nonhydrostatic conditions and compare these disequilibrium states with those predicted by phase diagrams derived from static experiments under equilibrium conditions. We create highly dynamic conditions utilizing a mDAC and study the phase transformations in α-quartz in situ by synchrotron powder X-ray diffraction. Phase transitions ofmore » α-quartz are studied at pressures up to 66.1 and different loading rates. At compression rates between 0.14 and 1.96 GPa s -1, experiments reveal that α-quartz is amorphized and partially converted to stishovite between 20.7 GPa and 28.0 GPa. Therefore, coesite is not formed as would be expected from equilibrium conditions. With the increasing compression rate, a slight increase in the transition pressure occurs. The experiments show that dynamic compression causes an instantaneous formation of structures consisting only of SiO 6 octahedra rather than the rearrangement of the SiO 4 tetrahedra to form a coesite. Although shock compression rates are orders of magnitude faster, a similar mechanism could operate in impact events.« less
Carl, Eva-Regine; Mansfeld, Ulrich; Liermann, Hanns-Peter; ...
2017-03-27
Hypervelocity collisions of solid bodies occur frequently in the solar system and affect rocks by shock waves and dynamic loading. A range of shock metamorphic effects and high-pressure polymorphs in rock-forming minerals are known from meteorites and terrestrial impact craters. In this paper, we investigate the formation of high-pressure polymorphs of α-quartz under dynamic and nonhydrostatic conditions and compare these disequilibrium states with those predicted by phase diagrams derived from static experiments under equilibrium conditions. We create highly dynamic conditions utilizing a mDAC and study the phase transformations in α-quartz in situ by synchrotron powder X-ray diffraction. Phase transitions ofmore » α-quartz are studied at pressures up to 66.1 and different loading rates. At compression rates between 0.14 and 1.96 GPa s -1, experiments reveal that α-quartz is amorphized and partially converted to stishovite between 20.7 GPa and 28.0 GPa. Therefore, coesite is not formed as would be expected from equilibrium conditions. With the increasing compression rate, a slight increase in the transition pressure occurs. The experiments show that dynamic compression causes an instantaneous formation of structures consisting only of SiO 6 octahedra rather than the rearrangement of the SiO 4 tetrahedra to form a coesite. Although shock compression rates are orders of magnitude faster, a similar mechanism could operate in impact events.« less
Phase Equilibria Modeling of Coesite Eclogite from the Sulu Belt, Eastern China
NASA Astrophysics Data System (ADS)
Xia, B.; Brown, M.; Wang, L.; Wang, S.; Piccoli, P. M.
2016-12-01
Modeling of phase equilibria and tectonic processes are essential components to understand controls on P-T paths of UHPM rocks. However, diffusion at higher temperatures (> 700 °C), and issues with determination of Fe3+ in minerals and estimating H2O contents limit our ability to determine prograde, peak P and retrograde P-T data. Also, the lack of an appropriate activity-composition model for melt in basic rocks has limited the application of phase equilibria modeling to understand partial melting associated with exhumation. Here we apply phase equilibria modeling to coesite eclogite from Yangkou to assess the influence of Fe3+ and fluid during metamorphism, monitor reactions and phase relations in eclogite during deep subduction and exhumation and investigate partial melting at HP conditions. The modeling used the THERMOCALC software and the new internally consistent thermodynamic dataset for basic rocks (http://www.metamorph.geo.uni-mainz.de/thermocalc/dataset6/index.html). Here we investigate bimineralic (gt+omp+coe/qz+ru/ilm), phengite-bearing (gt+omp+phen (2 samples, <5 vol% and >5 vol%) +coe/qz+ru/ilm) and kyanite-bearing (gt+omp+phen+ky+coe/qz+ru/ilm) eclogites. Coesite in the matrix is the hallmark of the Yangkou eclogite. For each sample, we use an iterative process to estimate the H2O and O content in the bulk composition, and then calculate a P-T pseudosection. The results suggest that some prograde information (670-770 °C, > 3.0 GPa) is retained in large garnet cores in bimineralic and phengite-bearing eclogite. The peak P-T conditions are a challenge because in the field of gt+omp+coe/qz±phen+H2O at T > 750 °C and P > 3.5 GPa mode and compositional changes are small. However, isopleths of Si in phengite suggest that the peak P could have been > 5-6 GPa. Re-equilibration of garnet and omphacite compositions occurred during exhumation, yielding P-T conditions of 700-790 °C at 3.1-2.0 GPa. Amphibolite facies metamorphism occurred at 630-710 °C, 1.3-1.2 GPa. The retrograde P-T path passes through the suprasolidus field; however, the melt produced is very low (< 5 mol%). Our work provides new quantitative P-T data for UHP eclogite in the Sulu belt and contributes to further understanding of the processes that affect deeply subducted continental crust.
UHP metamorphism in Greece: Petrologic data from the Rhodope Mountains
NASA Astrophysics Data System (ADS)
Baziotis, I. P.; Mposkos, E.; Krohe, A.; Wawrzenitz, N. H.; Liu, Y.; Taylor, L. A.
2012-12-01
Metamorphic rocks contain invaluable information for understanding the orogenic mechanisms of a tectonic regime. It is now well recorded and recognized that subduction of oceanic lithosphere and collision of continental blocks can result in sinking of subducted rocks to deeper levels than normal (>100 km). Further, the discovery of coesite and diamond in apparently regionally metamorphosed rocks provoked issues, for returning these rocks to the surface relatively fast, thereby preserving the UHP conditions. These UHPM terrains have been identified in more than twenty provinces worldwide. In Greece, UHPM rocks occur in the Rhodope area, one of the major tectono-metamorphic units located in NE Greece. This region consists of different metamorphic complexes involved in the Alpine collisional history between the Eurasian and African plates (e.g., Krohe & Mposkos, 2002-Geol Soc London Spec Pub, 204, 151). In Rhodope, a Jurassic UHP metamorphism is confirmed in the uppermost Kimi and the underlying Sidironero complexes (Mposkos & Kostopoulos, 2001- EPSL, 192, 497; Perraki et al., 2004-5th ISEMG, T2-35, 2006- EPSL, 241, 672; Liati, 2005- Con Min Pet, 150, 608; Bauer et al., 2007- Lithos, 99, 207). UHP metamorphism is evidenced by the presence of octahedral microdiamond inclusions (3 to 10 μm) in protective garnets, within the metapelitic gneisses. Microdiamonds probably formed from a supercritical fluid under extreme P-T conditions. The latter is strengthened by the presence of composite inclusions consisting of CO2, calcite, and microdiamonds. Other UHP indicators include: 1) quartz rods and rutile needle exsolutions in metapelitic garnet, suggesting a former titaniferous super-silicic (majoritic) garnet formed at P >4GPa; 2) oriented quartz lamellae in eclogitic clinopyroxene having been exsolved from a former super-silicic UHP precursor; and 3) coesite pseudomorphs in garnet, where radial cracks around multi-crystalline-quartz aggregates are indicative of the former coesite existence (e.g., Mposkos & Krohe, 2006- Can J Earth Sci, 43, 1755). Jurassic UHP rocks are overprinted by late Jurassic/early Cretaceous HP granulite facies metamorphism (P >1.5GPa; T~900 oC). In the Eastern and Western Rhodope, exhumation of these rocks occurred along different P-T paths. In the eastern Rhodope (Kimi Complex), UHP rocks re-equilibrated under relatively static annealing conditions and emerged at the surface in the Eocene. In the western Rhodope (Sidironero Complex), these rocks have been subjected to an overprinting Eocene MP to HP metamorphism, followed by exhumation along a major shear zone at about 40 Ma. In either case, a long-lasting post-UHP metamorphic history retrograded and almost completely destroyed the UHP minerals, thereby limiting the UHP record mainly to textural evidences and scarce UHP polymorphs. Consequently, some of the micro-diamonds have been partially or fully graphitized during this extensive exhumation period.
Thermal Conductivity Measurement of Synthesized Mantle Minerals
NASA Astrophysics Data System (ADS)
Asimow, P. D.; Luo, S.; Mosenfelder, J. L.; Liu, W.; Staneff, G. D.; Ahrens, T. J.; Chen, G.
2002-12-01
Direct thermal conductivity (k) measurement of mantle minerals is crucial to constrain the thermal profile of the Earth as well as geodynamic studies of the mantle (e.g., to determine the Rayleigh number). We have embarked on systematic multi-anvil syntheses of dense polycrystalline specimens of mantle phases of adequate size and zero porosity for precise thermal conductivity measurements by the 3ω method (\\textit{Cahill and Pohl, Phys. Rev. B, 1987}) under elevated temperatures (T). Coesite and stishovite (see \\textit{Luo et al., GRL, 2002}) as well as majorite and wadsleyite have been synthesized; ringwoodite and perovskite are scheduled. Preliminary thermal conductivity measurements at ambient pressure on coesite (120 - 300 K, 9.53 Wm-1K-1 at 300 K) are consistent with prior room temperature data (\\textit{Yukutake & Shimada, PEPI, 1978}), while our stishovite data at 300 K appear to be low (1.96 Wm-1K-1). Efforts are being made to extend the measurement to higher temperatures (e.g., above Debye temperature Θ D), thus allowing determination of k(T) relationship (say, k~ T-n); success will depend on the decomposition kinetics of these metastable phases. The pressure dependence of k of these synthesized samples can also be measured (\\textit{e.g., Osako et al., HPMPS-6, 2002; Xu et al., EOS, 2001}). Recent thermal conductivity measurement on LiF and Al2O_3 from shock wave loading (\\textit{Holland & Ahrens, 1998}) is consistent with the modeling on MgO and Al2O_3 (\\textit{Manga & Jeanloz, JGR, 1997}) with classical theories. Thus, k values at modest pressures and T (say, above Θ D) would allow extrapolation of k to appropriate mantle conditions.
NASA Astrophysics Data System (ADS)
Lang, Helen M.; Gilotti, Jane A.
2015-06-01
Pseudosection modeling constrains the pressure-temperature (P-T) exhumation path of partially melted ultrahigh-pressure (UHP) metapelites exposed in the North-East Greenland UHP terrane. A robust peak P and T estimate of 3.6 GPa and 970 °C based on mineral assemblages in nearby kyanite eclogites is the starting point for the P-T path. Although the peak assemblage for the metapelite is not preserved, the calculated modeled peak assemblage contained substantial clinopyroxene, garnet, phengite, K-feldspar and coesite with minor kyanite and rutile. Combining the pseudosection and observed textures, the decompression path crosses the coesite-quartz transition before reaching the dry phengite dehydration melting reaction where phengite is abruptly consumed. In the range of 2.5 to 2.2 GPa, clinopyroxene is completely consumed and garnet grows to its maximum volume and grossular content, matching the high grossular rims of relict megacrysts. Plagioclase joins the assemblage and the pseudosection predicts up to 12-13 vol.% melt in the supersolidus assemblage, which contained garnet, liquid, K-feldspar, plagioclase, kyanite, quartz and rutile. At this stage, the steep decompression path flattened out and became nearly isobaric. The melt crystallization assemblage that formed when the path crossed the solidus with decreasing temperature contains phengite, garnet, biotite, 2 feldspars, kyanite, quartz and rutile. Therefore, the path must have intersected the solidus at approximately 1.2 GPa, 825 °C. The pseudosection predicts that garnet is consumed on the cooling path, but little evidence of late garnet consumption or other retrograde effects is observed. This may be due to partial melt loss from the rock. Isochemical PT-n and PT-X sections calculated along the P-T path display changes in mineral assemblage and composition that are consistent with preserved assemblages.
Metamorphism of eclogites from the UHP Maksyutov Complex, south Ural Mountains, Russia
NASA Astrophysics Data System (ADS)
Burlick, T. D.; Leech, M. L.
2013-12-01
The Maksyutov Complex is a mid- to late Paleozoic ultrahigh-pressure (UHP) subduction terrane in the south Ural Mountains of Russia. Radial fractures around quartz inclusions in garnet, omphacite, and glaucophane interpreted as pre-existing coesite; and microdiamond aggregates in garnet identified by Raman spectroscopy demonstrate Maksyutov rocks were subducted to UHP conditions (>2.8 GPa for coesite and >3.0 GPa for diamond at 600°C). Peak UHP eclogite-facies metamorphism (Grt+Omp+Ph+Coe+Rt ×Ttn) took place at c. 385 M and Maksyutov rocks were exhumed through retrograde blueschist-facies metamorphism (Grt+Gln+Ph+Qz×Chl×Ep) by 360 Ma. Pseudosections were constructed to constrain the P-T conditions recorded by the equilibrium mineral assemblanges in eclogites and their retrograded equivalents using bulk rock XRF analysis in the system Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O-TiO2 and the suite of free energy minimization programs, Perple_X 6.6.8 [Connolly 2009] with the internally consistent end-member thermodynamic database from Holland and Powell [1998] (mod 2004); solution models for omphacite (Holland and Powell, 1996), clinoamphibole (Dale et al. 2005), white mica (Coggon & Holland 2002, Auzanneau et al 2010), chlorite and garnet (Holland and Powell 1998; Powell and Holland 1999), and feldspar (Thompson and Hovis 1979; Newton et al. 1980) were used with H2O as a saturated component. Both conventional thermometry, using microprobe analyses and Grt-Cpx cation exchange as well as pseudosection modeling result in higher peak equilibrium temperatures than has been previously been reported in the Maksyutov. Pseudosection modeling gives minimum P-T conditions of 625°-675°C and 2.8-3.1 GPa for peak assemblages from the least retrogressed eclogites, while Fe-Mg exchange thermometry yields temperatures of 775°C × 25°C for pressures ranging from 2.5 to 3.5 GPa.
NASA Astrophysics Data System (ADS)
Wang, Songjie; Wang, Lu
2015-04-01
Barite (BaSO4) is well-known from deep-sea sedimentary environments but has received less attention to its presence in high-grade metamorphic rocks. Recently, barite in ultrahigh pressure (UHP) eclogite has drawn increasing attention from geologists, especially in the Dabie-Sulu orogen, since it is an important indicator for high-salinity fluid events, thus aiding in further understanding HP-UHP fluid / melt evolution. However, its formation time and mechanism in UHP eclogite are still controversial, with three representative viewpoints: (1) Liu et al. (2000) found barite-anhydrite-coesite inclusions in zircon and interpreted them to have formed by UHP metamorphic fluids; (2) Zeng et al. (2007) recognized isolated barite within K-feldspar (Kfs) and Quartz (Qz) surrounded by radial cracks in omphacite, and interpreted Kfs+Qz to be reaction products of potassium-rich fluid/melt and coesite, with the barite formed by prograde metamorphic fluids; (3) Gao et al. (2012) and Chen et al. (2014) found barite-bearing Multiphase Solid (MS) inclusions within garnet and omphacite and assumed that the barite formed by phengite breakdown possibly caused by eclogite partial melting during exhumation, though no direct evidence were proposed. The controversy above is mainly due to the lack of direct formation evidence and absence of a clear link with the metamorphic evolution of UHP eclogite along the subduction-exhumation path. We report detailed petrological and micro-structural analyses revealing four types of barites clearly linked with (1) the prograde, (2) earlier stage of partial melting and (3) later stage of crystallization differentiation, as well as (4) high-grade amphibolite-facies retrogression of a deeply subducted and partially melted intergranular coesite-bearing eclogite from Yangkou Bay, Sulu Orogen. Round barite inclusions (type-I) within UHP-stage garnet and omphacite are formed by internally buffered fluids from mineral dehydration during prograde metamorphism. Zr-in-rutile thermometry shows their formation temperature to be 586-664 oC at 1.5-2.5 GPa. Barite-bearing MS inclusions with Ba-bearing K-feldspar (type-II) connected by Kfs+Pl+Bt veinlets of in-situ phengite breakdown and thin barite veinlets along grain boundaries (type-III) are products of phengite breakdown and induced fluid flow during exhumation. These barites have witnessed the gradational separation process of melt/ fluid from miscibility on/above the second critical endpoint during UHP metamorphism, to immiscibility along the exhumation path of the subducted slab. Associated reactions from pyrite to hematite and goethite with the type-III barite ring surrounding the pyrite provide evidence for a local high oxygen fugacity environment during eclogite partial melting and subsequent melt/fluid crystallization processes. Moreover, large grain barite aggregations (type-IV) modified by amphibole+albite symplectite are most likely formed by release of molecular and hydroxyl water from anhydrous minerals of eclogite during high-grade amphibolite-facies retrogression. The growth of multi-stage barites in UHP eclogite further advances our understanding of fluid/melt transfer, crystallization processes along the subduction-exhumation path of the partially melted eclogite, broadening our knowledge of melt/fluid evolution within subduction-collision zones worldwide. REFERENCES Chen Y.X., et al., 2014, Lithos, 200, 1-21. Liu J.B., et al., 2000, Acta Petrologica Sinica 16(4), 482-484. Zeng L.S., et al., 2007, Chinese Science Bulletin, 52(21), 2995-3001. Gao X.Y., et al., 2012, Journal of Metamorphic Geology, 30(2), 193-212.
NASA Astrophysics Data System (ADS)
Wu, Xiaoyu; Chang, Hector; Mello, Charlene; Nagarajan, Ramanathan; Narsimhan, Ganesan
2013-01-01
Explicit solvent molecular dynamics (MD) simulation was carried out for the antimicrobial peptides (i) Cecropin P1 and C-terminus cysteine modified Cecropin P1 (Cecropin P1 C) in solution, (ii) Cecropin P1 and Cecropin P1 C adsorbed onto coesite -Si - O - and Si - O - H surfaces, and (iii) Cecropin P1 C tethered to coesite -Si - O - surface with either (PEO)3 or (PEO)6 linker. Low energy structures for Cecropin P1 and Cecropin P1 C in solution consists of two regions of high α helix probability with a sharp bend, consistent with the available structures of other antimicrobial peptides. The structure of Cecropin P1 C at low ionic strength of 0.02 M exhibits two regions of high α helix probability (residues AKKLEN and EGI) whereas at higher ionic strength of 0.12 M, the molecule was more compact and had three regions of higher α helix probability (residues TAKKLENSA, ISE, and AIQG) with an increase in α helical content from 15.6% to 18.7% as a result of shielding of electrostatic interactions. In the presence of Cecropin P1 C in the vicinity of -Si - O - surface, there is a shift in the location of two peaks in H - O - H density profile to larger distances (2.95 Å and 7.38 Å compared to 2.82 Å and 4.88 Å in the absence of peptide) with attenuated peak intensity. This attenuation is found to be more pronounced for the first peak. H-bond density profile in the vicinity of -Si - O - surface exhibited a single peak in the presence of Cecropin P1 C (at 2.9 Å) which was only slightly different from the profile in the absence of polypeptide (2.82 Å) thus indicating that Cecropin P1 C is not able to break the H-bond formed by the silica surface. The α helix probability for different residues of adsorbed Cecropin P1 C on -Si - O - surface is not significantly different from that of Cecropin P1 C in solution at low ionic strength of 0.02 M whereas there is a decrease in the probability in the second (residues ISE) and third (residues AIQG) α helical regions at higher ionic strength of 0.12 M. Though the total α helical content of adsorbed and tethered Cecropin P1 C was lower for hydrophilic Si - O - H surface compared to hydrophobic -Si - O -, hydrophobicity of the surface did not significantly affect the α helix probability of different residues. The conformation of Cecropin P1 C in solution is closer to that of tethered to -Si - O - with (PEO)6 than that tethered with (PEO)3 as a result of less surface interaction of tethered polypeptide with a longer linker. At low ionic strength of 0.02 M, tethered Cecropin P1 C to -Si - O - is found to exhibit lower α helix (13.0%) compared to adsorbed (15.6%) for (PEO)3 linker with this difference being insignificant for larger (PEO)6 linker molecule. Experimental values of % α helix inferred from circular dichroism spectra of Cecropin P1 in solution as well as in adsorbed state on silica surface compared well with the corresponding values obtained from MD simulation thereby validating the simulation procedure.
Wu, Xiaoyu; Chang, Hector; Mello, Charlene; Nagarajan, Ramanathan; Narsimhan, Ganesan
2013-01-28
Explicit solvent molecular dynamics (MD) simulation was carried out for the antimicrobial peptides (i) Cecropin P1 and C-terminus cysteine modified Cecropin P1 (Cecropin P1 C) in solution, (ii) Cecropin P1 and Cecropin P1 C adsorbed onto coesite -Si - O - and Si - O - H surfaces, and (iii) Cecropin P1 C tethered to coesite -Si - O - surface with either (PEO)(3) or (PEO)(6) linker. Low energy structures for Cecropin P1 and Cecropin P1 C in solution consists of two regions of high α helix probability with a sharp bend, consistent with the available structures of other antimicrobial peptides. The structure of Cecropin P1 C at low ionic strength of 0.02 M exhibits two regions of high α helix probability (residues AKKLEN and EGI) whereas at higher ionic strength of 0.12 M, the molecule was more compact and had three regions of higher α helix probability (residues TAKKLENSA, ISE, and AIQG) with an increase in α helical content from 15.6% to 18.7% as a result of shielding of electrostatic interactions. In the presence of Cecropin P1 C in the vicinity of -Si - O - surface, there is a shift in the location of two peaks in H - O - H density profile to larger distances (2.95 Å and 7.38 Å compared to 2.82 Å and 4.88 Å in the absence of peptide) with attenuated peak intensity. This attenuation is found to be more pronounced for the first peak. H-bond density profile in the vicinity of -Si - O - surface exhibited a single peak in the presence of Cecropin P1 C (at 2.9 Å) which was only slightly different from the profile in the absence of polypeptide (2.82 Å) thus indicating that Cecropin P1 C is not able to break the H-bond formed by the silica surface. The α helix probability for different residues of adsorbed Cecropin P1 C on -Si - O - surface is not significantly different from that of Cecropin P1 C in solution at low ionic strength of 0.02 M whereas there is a decrease in the probability in the second (residues ISE) and third (residues AIQG) α helical regions at higher ionic strength of 0.12 M. Though the total α helical content of adsorbed and tethered Cecropin P1 C was lower for hydrophilic Si - O - H surface compared to hydrophobic -Si - O -, hydrophobicity of the surface did not significantly affect the α helix probability of different residues. The conformation of Cecropin P1 C in solution is closer to that of tethered to -Si - O - with (PEO)(6) than that tethered with (PEO)(3) as a result of less surface interaction of tethered polypeptide with a longer linker. At low ionic strength of 0.02 M, tethered Cecropin P1 C to -Si - O - is found to exhibit lower α helix (13.0%) compared to adsorbed (15.6%) for (PEO)(3) linker with this difference being insignificant for larger (PEO)(6) linker molecule. Experimental values of % α helix inferred from circular dichroism spectra of Cecropin P1 in solution as well as in adsorbed state on silica surface compared well with the corresponding values obtained from MD simulation thereby validating the simulation procedure.
NASA Astrophysics Data System (ADS)
Toft, Paul B.; Hills, Doris V.; Haggerty, Stephen E.
1989-04-01
A petrographic, mineral and bulk chemical study of a xenolith suite of granulites and eclogites from Sample Creek, Liberia and Koidu, Sierra Leone, has been undertaken with a view to determining the nature of the crust-upper mantle interface. A broad range of xenolith compositions is present (from high-MgO eclogites to garnet-anorthosites) and a systematic AFM trend is established, consistent with mafic and ultramafic melt fractionation at moderate pressures (10-20 kbar). A trend is established for the entire xenolith suite among bulk chemistry, seismic P-wave velocity and a crust/mantle (C/M) bulk chemical ratio defined as Na 2O + K 2O + SiO 2/FeO + MgO mole %. Three populations are present: a granulitic crustal group ( SG < 3.0; VP = 6.6-7.2 km/ s; C/ M > 3.0); a granulite and eclogite transitional group ( SG 3.0-3.3; VP = 7.2-8.0 km/ s; C/ M 1.5-3.0); andanexclusivelyuppermantleeclogiticgroup ( ifSG > 3.3; VP = 8.2-8.7 km/ s; C/ M ~ 1.5). From these data and coupled with garnet-clinopyroxene mineral thermometry and accessory phases (e.g., diamond, graphite, coesite, kyanite) or the presence of plagioclase, a xenolith geotherm is established based on stratigraphic sequencing and phase transition boundaries. Diamond and coesite-bearing eclogites conform to the 40 mW/m 2 standard cratonic low heat flow geotherm, whereas the plagioclase granulites at lower pressures correspond to an average rift geotherm of 90 mW/m 2. The latter is ascribed to igneous underplating onto the lower crust or to thermal perturbations from an earlier tectonic event. Graphite and kyanite eclogites and the transitional group (in SG, VP and C/M ratio) of eclogites and granulites fall between the 40 and 90 mW/m 2 reference geotherms. The xenoliths are meta-igneous, the lower crust and uppermost mantle are mafic in composition and the petrologic Moho is an intercalated, interstratified horizon of eclogite and garnet granulite. Growth of the early crust was largely a consequence of asthenospheric depletion in which underplating rather than lateral accretion was dominant.
NASA Astrophysics Data System (ADS)
Liu, Xi; Ma, Yunlu; He, Qiang; He, Mingyue
2017-10-01
Coesite (Coe) with grain size in the range of 30-80 μm has been synthesized at 5 GPa and 1600 °C for 12 h by using a cubic press. Its unpolarized single-crystal absorption infrared (IR) spectra show 14 IR bands in the range of ∼1200-650 cm-1, five of which have high intensity (at ∼1161, 1109, 1063, 1028 and 994 cm-1) and are preliminarily assigned to the SiO4 asymmetric stretching (ν3). In addition, three sharp but relatively weak bands at ∼838, 814 and 796 cm-1 are tentatively attributed to the SiO4 asymmetric bending (ν4). The IR data also show six OH peaks in the range of 3700-3300 cm-1, with an estimated H2O content of ∼30(4) wt ppm. Following previous studies, we have assigned the peaks at ∼3464 (#7), 3421 (#8), 3406 (#9) and 3377 cm-1 (#10) to the Type-II hydrogarnet substitution, and the peaks at ∼3500 (#6a) and 3534 cm-1 (#6b) to the B-based defects, with the latter aroused by possible B contamination in the synthesizing experiments. Annealing experiments conducted consecutively at ∼200, 400, 600, 800, 1000 and 1200 °C, with every heating step lasting for 24 h, demonstrate that water diffuses quickly out of Coe at T as low as ∼600 °C. The material annealed at 1200 °C is completely dehydrated and amorphous. A quick response of the water content in Coe to the changes of P, T and composition is thus possible, which may be critical to the preservation of natural Coe in relevant geological processes. It further implies that water in Coe, and possibly in other nominally anhydrous minerals (NAMs), may behave distinctively different from the water located in the hydrous phases such as amphibole and mica, and potentially makes significant contribution to the subduction zone-related fluids.
Fubini, B; Bolis, V; Cavenago, A; Volante, M
1995-01-01
The effect of grinding, heating, and etching was investigated on polymorphs of silicon dioxide exhibiting different biological responses. Diatomaceous earths were converted into cristobalite at 1000 degrees C. Dusts obtained by grinding crystalline minerals exhibited different micromorphology and a propensity to originate surface radicals which decrease in the sequence cristobalite --> quartz --> coesite --> stishovite. The production of surface radicals was suppressed by grinding in the presence of water. Thermal treatments selectively quenched the radicals and decreased surface hydrophilicity. Quartz treated with aluminum lactate exhibited higher surface acidity when compared with pure quartz, with a reduction in fibrogenicity. Etching by hydrofluoric acid smoothed the particles with loss of specific surface. Adsorption of water on three cristobalite dusts of different origin (ground mineral, ex-diatomite, heated quartz) indicated a loss in heated quartz (1300 degrees C) that was relatable to the corresponding reduction in fibrogenicity.
NASA Astrophysics Data System (ADS)
Glass, Billy P.; Koeberl, Christian
2006-02-01
Australasian microtektites were discovered in Ocean Drilling Program (ODP) Hole 1143A in the central part of the South China Sea. Unmelted ejecta were found associated with the microtektites at this site and with Australasian microtektites in Core SO95-17957-2 and ODP Hole 1144A from the central and northern part of the South China Sea, respectively. A few opaque, irregular, rounded, partly melted particles containing highly fractured mineral inclusions (generally quartz and some K feldspar) and some partially melted mineral grains, in a glassy matrix were also found in the microtektite layer. The unmelted ejecta at all three sites include abundant white, opaque grains consisting of mixtures of quartz, coesite, and stishovite, and abundant rock fragments which also contain coesite and, rarely, stishovite. This is the first time that shock-metamorphosed rock fragments have been found in the Australasian microtektite layer. The rock fragments have major and trace element contents similar to the Australasian microtektites and tektites, except for higher volatile element contents. Assuming that the Australasian tektites and microtektites were formed from the same target material as the rock fragments, the parent material for the Australasian tektites and microtektites appears to have been a fine-grained sedimentary deposit. Hole 1144A has the highest abundance of microtektites (number/cm2) of any known Australasian microtektite-bearing site and may be closer to the source crater than any previously identified Australasian microtektite-bearing site. A source crater in the vicinity of 22° N and 104° E seems to explain geographic variations in abundance of both the microtektites and the unmelted ejecta the best; however, a region extending NW into southern China and SE into the Gulf of Tonkin explains the geographic variation in abundance of microtektites and unmelted ejecta almost as well. The size of the source crater is estimated to be 43 ± 9 km based on estimated thickness of the ejecta layer at each site and distance from the proposed source. A volcanic ash layer occurs just above the Australasian microtektite layer, which some authors suggest is from a supereruption of the Toba caldera complex. We estimate that deposition of the ash occurred ˜800 ka ago and that it is spread over an area of at least 3.7 × 107 km2.
NASA Astrophysics Data System (ADS)
Butler, J. P.; Jamieson, R. A.; Dunning, G. R.; Pecha, M. E.; Robinson, P.; Steenkamp, H. M.
2018-06-01
We present the results of a combined CA-ID-TIMS and LA-MC-ICP-MS U-Pb geochronology study of zircon and associated rutile and titanite from the Nordøyane ultra-high-pressure (UHP) domain in the Western Gneiss Region (WGR) of Norway. The dated samples include 4 eclogite bodies, 2 host-rock migmatites, and 2 cross-cutting pegmatites and leucosomes, all from the island of Harøya. Zircon from a coesite eclogite yielded an age of ca. 413 Ma, interpreted as the time of UHP metamorphism in this sample. Zircon data from the other eclogite bodies yielded metamorphic ages of ca. 413 Ma, 407 Ma, and 406 Ma; zircon trace-element data associated with 413 Ma and 407 Ma ages are consistent with eclogite-facies crystallization. In all of the eclogites, U-Pb dates from zircon cores, interpreted as the times of protolith crystallization, range from ca. 1680-1586 Ma, consistent with Gothian ages from orthogneisses in Nordøyane and elsewhere in the WGR. A zircon core age of ca. 943 Ma from one sample agrees with Sveconorwegian ages of felsic gneisses and pegmatites in the western part of the area. Migmatites hosting the eclogite bodies yielded zircon core ages of ca. 1657-1591 Ma and rim ages of ca. 395-392 Ma, interpreted as the times of Gothian protolith formation and Scandian partial melt crystallization, respectively. Pegmatite in an eclogite boudin neck yielded a crystallization age of ca. 388 Ma, interpreted as the time of melt crystallization. Rutile and titanite from 3 samples (an eclogite and two migmatites) yielded concordant ID-TIMS ages of 378-376 Ma. The results are similar to existing U-Pb data from other Nordøyane eclogites (415-405 Ma). In combination with previous pressure-temperature data from the coesite eclogite, these ages indicate that peak metamorphic conditions of 3 GPa/760 °C were reached ca. 413 Ma, followed by decompression to 1 GPa/810 °C by ca. 397 Ma and cooling below ca. 600 °C by ca. 375 Ma. The results are compatible with protracted UHP metamorphism followed by relatively slow exhumation. The question of whether partial melting began at UHP conditions is not resolved by this study.
McClelland, W.C.; Gilotti, J.A.; Mazdab, F.K.; Wooden, J.L.
2009-01-01
Coesite-bearing zircon formed at ultrahigh-pressure (UHP) conditions share general characteristics of eclogite-facies zircon with trace-element signatures characterized by depleted heavy rare earth elements (HREE), lack of an Eu anomaly, and low Th/ U ratios. Trace-element signatures of zircons from the Caledonian UHP terrane in North-East Greenland were used to examine the possible changes in signature with age during exhumation. Collection and interpretation of age and trace-element analyses of zircon from three samples of quartzofeldspathic gneiss and two leucocratic intrusions were guided by core vs. rim zoning patterns as imaged by cathodoluminesence. Change from igneous to eclogite-facies metamorphic trace-element signature in protolith zircon is characterized by gradual depletion of HREE, whereas newly formed metamorphic rims have flat HREE patterns and REE concentrations that are distinct from the recrystallized inherited cores. The signature associated with eclogite-facies metamorphic zircon is observed in coesite-bearing zircon formed at 358 ?? 4 Ma, metamorphic rims formed at 348 ?? 5 Ma during the initial stages of exhumation, and metamorphic rims formed at 337 ?? 5 Ma. Zircons from a garnet-bearing granite emplaced in the neck of an eclogite boudin and a leucocratic dike that cross-cuts amphibolite-facies structural fabrics have steeply sloping HREE patterns, variably developed negative Eu anomalies, and low Th/U ratios. The granite records initial decompression melting and exhumation at 347 ?? 2 Ma and later zircon rim growth at 329 ?? 5. The leucocratic dike was likely emplaced at amphibolite-facies conditions at 330 ?? 2 Ma, but records additional growth of compositionally similar zircon at 321 ??2 Ma. The difference between the trace-element signature of metamorphic zircon in the gneisses and in part coeval leucocratic intrusions indicates that the zircon signature varies as a function of lithology and context, thus enhancing its ability to aid in the interpretation of U-Pb data and track the exhumation history of UHP terranes. The differences may reflect variation in elemental availability through breakdown reactions in quartzofeldpathic gneiss vs. availability during melt production and/or crystallization. UHP rocks in North-East Greenland began exhumation by 347 ?? 2 Ma, were still at HP eclogite-facies conditions at 337 ?? 5 Ma and were at amphibolite-facies conditions by 330 ?? 2 Ma. ?? 2009 E. Schweizerbart'sche Verlagsbuchhandlung.
NASA Technical Reports Server (NTRS)
Boslough, M. B.; Cygan, R. T.; Kirkpatrick, R. J.
1993-01-01
We have applied solid state Si-29 nuclear magnetic resonance (NMR) spectroscopy to five naturally-shocked Coconino Sandstone samples from Meteor Crater, Arizona, with the goal of examining possible correlations between NMR spectral characteristics and shock level. This work follows our observation of a strong correlation between the width of a Si-29 resonance and peak shock pressure for experimentally shocked quartz powders. The peak width increase is due to the shock-induced formation of amorphous silica, which increases as a function of shock pressure over the range that we studied (7.5 to 22 GPa). The Coconino Sandstone spectra are in excellent agreement with the classification scheme of Kieffer in terms of presence and approximate abundances of quartz, coesite, stishovite, and glass. We also observe a new resonance in two moderately shocked samples that we have tentatively identified with silicon in tetrahedra with one hydroxyl group in a densified form of amorphous silica.
NASA Technical Reports Server (NTRS)
White, J. C.
1992-01-01
High-pressure silica polymorphs (coesite and stishovite) were described from the Vredefort structure in association with pseudotachylite veinlets. In addition to the fundamental significance of the polymorphs to genetic interpretations of the structure, it was additionally argued that the type of pseudotachylite with which they occur forms during the compressional phase of the shock process, while the larger, classic pseudotachylite occurrences are barren of polymorphs and formed during passage of the rarefaction wave. This identification of temporal relationships among transient shock features at a regional scale is similar to observations from the Manicouagan structure, Quebec, where texturally distinct diaplectic plagioclase glasses formed during both compressional and decompressional phases of the shock process. The clarification of such relationships impinges directly on interpretations of natural shock processes and the identification of high probability targets for polymorph searches. Detailed analytical scanning (SEM) and transmission electron microscopy (TEM) were utilized to further establish the nature of both the pseudotachylite and the silica polymorph occurrences in the Vredefort rocks. The results of this investigation are discussed.
NASA Astrophysics Data System (ADS)
Proyer, A.; Mposkos, E.; Baziotis, I.; Hoinkes, G.
2008-08-01
Four different types of parageneses of the minerals calcite, dolomite, diopside, forsterite, spinel, amphibole (pargasite), (Ti-)clinohumite and phlogopite were observed in calcite-dolomite marbles collected in the Kimi-Complex of the Rhodope Metamorphic Province (RMP). The presence of former aragonite can be inferred from carbonate inclusions, which, in combination with an analysis of phase relations in the simplified system CaO-MgO-Al 2O 3-SiO 2-CO 2 (CMAS-CO 2) show that the mineral assemblages preserved in these marbles most likely equilibrated at the aragonite-calcite transition, slightly below the coesite stability field, at ca. 720 °C, 25 kbar and aCO 2 ~ 0.01. The thermodynamic model predicts that no matter what activity of CO 2, garnet has to be present in aluminous calcite-dolomite-marble at UHP conditions.
A Mapping of the Electron Localization Function for Earth Materials
DOE Office of Scientific and Technical Information (OSTI.GOV)
Gibbs, Gerald V.; Cox, David F.; Ross, Nancy
2005-06-01
The electron localization function, ELF, generated for a number of geometry-optimized earth materials, provides a graphical representation of the spatial localization of the probability electron density distribution as embodied in domains ascribed to localized bond and lone pair electrons. The lone pair domains, displayed by the silica polymorphs quartz, coesite and cristobalite, are typically banana-shaped and oriented perpendicular to the plane of the SiOSi angle at ~0.60 Å from the O atom on the reflex side of the angle. With decreasing angle, the domains increase in magnitude, indicating an increase in the nucleophilic character of the O atom, rendering itmore » more susceptible to potential electrophilic attack. The Laplacian isosurface maps of the experimental and theoretical electron density distribution for coesite substantiates the increase in the size of the domain with decreasing angle. Bond pair domains are displayed along each of the SiO bond vectors as discrete concave hemispherically-shaped domains at ~0.70 Å from the O atom. For more closed-shell ionic bonded interactions, the bond and lone pair domains are often coalesced, resulting in concave hemispherical toroidal-shaped domains with local maxima centered along the bond vectors. As the shared covalent character of the bonded interactions increases, the bond and lone pair domains are better developed as discrete domains. ELF isosurface maps generated for the earth materials tremolite, diopside, talc and dickite display banana-shaped lone pair domains associated with the bridging O atoms of SiOSi angles and concave hemispherical toroidal bond pair domains associated with the nonbridging ones. The lone pair domains in dickite and talc provide a basis for understanding the bonded interactions between the adjacent neutral layers. Maps were also generated for beryl, cordierite, quartz, low albite, forsterite, wadeite, åkermanite, pectolite, periclase, hurlbutite, thortveitite and vanthoffite. Strategies are reviewed for finding potential H docking sites in the silica polymorphs and related materials. As observed in an earlier study, the ELF is capable of generating bond and lone pair domains that are similar in number and arrangement to those provided by Laplacian and deformation electron density distributions. The formation of the bond and lone pair domains in the silica polymorphs and the progressive decrease in the SiO length as the value of the electron density at the bond critical point increases indicates that the SiO bonded interaction has a substantial component of covalent character.« less
NASA Astrophysics Data System (ADS)
Kotková, J.; Klapetek, P.
2012-04-01
Morphology, associated phases and retrogression phenomena of in-situ microdiamonds formed at extreme pressures in ultrahigh-pressure metamorphic terranes represent excellent tools to study character of diamond-forming media at great depths. Well-preserved microdiamonds discovered recently along with coesite in ultrahigh-pressure granulites of the north Bohemian crystalline basement, European Variscan belt (Kotková et al., 2011), provide unique material for such investigations. The diamonds are enclosed in major granulite phases, i.e. garnet both in felsic and intermediate lithologies and in kyanite in the felsic sample, as well as in zircon. Transmitted and reflected light microscopy of the felsic granulite sample, with peak mineral assemblage garnet, kyanite, feldspar and quartz, revealed presence of numerous, 5-20 μm-sized, perfectly preserved diamond crystals enclosed in kyanite grains. In contrast, diamonds within garnet are rare, can reach up to 30 μm in size, and graphite rims as well as polycrystalline graphite aggregates possibly representing complete diamond retrogression are common. We applied atomic force microscopy to study in-situ crystal morphology and surface microtopographic features, representing clues to the conditions and mechanisms of crystal formation as well as diamond resorption and retrogression. Both diamond enclosed in garnet and in kyanite of the felsic granulite occur exclusively as single crystals. The crystals have octahedral crystal shapes with straight but rounded edges and rounded corners. Concentric triangular terraces delimiting a flat triangular table on crystal scale and small micron-sized negatively oriented downward-pointing trigons developed on the octahedron crystal faces. Higher magnification reveals presence of discontinuous elongate hillocks oriented parallel to the octahedron face edge with positively oriented trigons. We suggest that the large-scale triangular terraces represent growth features. In contrast, the rounding of crystal edges and corners and development of negative trigons reflect diamond resorption. According to experimental works, such features are attributed to high temperature resorption, i.e. oxidation above ~ 950°C due to interaction with CO2 and/or H2O-bearing fluids (or fluid-bearing melts). Our results are consistent with presence of supercritical C-O-H fluid in the rocks in subduction zones documented from other ultrahigh-pressure metamorphic terranes, the resorption morphology corresponding rather to the interaction with water-rich than CO2-rich fluids. Kotková J., ÓBrien P., Ziemann M. (2011): Diamond and coesite discovered in Saxony-type granulite: Solution to the Variscan garnet peridotite enigma. Geology, 39, 7, 667-670.
Melting and dissolution of subducting crust at high pressures: the key role of white mica
NASA Astrophysics Data System (ADS)
Schmidt, Max W.; Vielzeuf, Daniel; Auzanneau, Estelle
2004-11-01
Conditions of melting in the crust are generally controlled by the availability of aqueous fluid and, in the absence of fluid, by the stability of hydroxylated minerals. To depths of 80-90 km, melting is controlled by amphibole and biotite. At greater depths, both phases are unstable in crustal compositions. Simultaneous experiments on a mid-ocean ridge basalt (MORB), a greywacke, and a pelite with excess H2O of 0.4-1.4 wt.% demonstrate that, at >100 km depth (≥3.5 GPa), all three bulk compositions are composed of garnet+clinopyroxene+phengite+coesite±kyanite±rutile, phengitic white mica being the only hydrous mineral present at near-melting temperatures. At 4 GPa, melting reactions, temperatures, and initial melt compositions are thus similar in the entire subducted crust. Fluid-saturated initial melting takes place near 850 °C and melt productivities are proportional to phengite contents. All three bulk compositions produce initially slightly peraluminous potassic Si-rich granites with K:Na molar ratios of 1.4-2.0 and containing 8-13 wt.% H2O. The relatively low Na-contents of these melts result from clinopyroxene/melt partitioning coefficients (Dcpx/melt) of 2.2-4.0 at near solidus temperatures. At higher pressures (≥6.5 GPa), we infer that classical melting does not take place. Instead, the bulk H2O-contents (1.5-2.1 wt.%) in the starting materials, although low, are apparently sufficient to dissolve phengite entirely near 1050 °C. This suggests that pressure conditions beyond the singular endpoint (or second critical point) which terminates the wet solidus as defined by Ricci in 1951 [J.E. Ricci, The phase rule and heterogeneous equilibrium, Dover Publications, Inc. New York (1951) 505 p.] were reached for all three bulk compositions. Extraction of these "supercritical" solute-rich (but Na-poor) melts, which contain about 30-40% H2O, or extraction of the potassic granite melts at lower pressure leave an anhydrous garnet+clinopyroxene±coesite±kyanite±rutile residue. Our results suggest that, except for extremely cold subduction zones, the subducting crust will lose all its potassium (and most of B, Be, Rb, and Ba, and other phengite-hosted trace elements) through leaching or melting during its descent to 300 km. The potassium-rich silica-saturated liquids will immediately react with the peridotite when entering the mantle wedge thus creating source regions for ultrapotassic magmas.
BARRINGER AWARD ADDRESS: Shock Metamorphism of Quartz in Nature and Experiment: A Review
NASA Astrophysics Data System (ADS)
Stoffler, D.
1993-07-01
Quartz as a widespread rock-forming mineral of the Earth's crust represents the most sensitive indicator of impact-induced shock waves and therefore provides an outstanding tool for the recognition of terrestrial impact formations and for the pressure calibration of shock metamorphosed rocks. This paper attempts to summarize the current knowledge in this field. Shocked quartz has been observed in quite variable spatial relations to impact craters: (1) in the crater basement, (2) in rock and mineral clasts of polymict breccias, and (3) in distal ejecta such as tektites and global air- fall beds (e.g., K/T boundary). Quartz displays a wide variety of shock- induced mechanical deformations and transformations [1,2]. Microscopically observable effects are multiple sets of planar fractures (PF) and planar deformation features (PDF) parallel to low indices crystallographic planes; mosaickism; reduced refractivity and birefringence; partial transformation to stishovite; increased optic axial angle; amorphization (diaplectic glass), partial transformation to coesite; and melting (lechatelierite). Additional effects at the atomic scale are well documented by TEM, X-ray diffraction and spectroscopy [3-7]. All types of shock effects observed so far in natural quartz have been reproduced by experimental shock waves in the laboratory and in large scale TNT and nuclear explosions. By means of sophisticated techniques the pressure dependence of shock effects has been calibrated with high precision. Threshold pressures at room temperature (given in GPa) for the onset of certain effects in single crystals and in nonporous quartzofeldpathic rocks are: 7.5 +- 2, 10 +- 2, 20 +- 2 (various PFs and PDFs), 12 +- 1 (stishovite), 25 +- 1 (reduced refractive index and density), ~30 (coesite), 34 +- 1 (total transformation to diaplectic glass), 50 +- 2 (melting and formation of lechatelierite) [8-12]. The type of shock effects, their paragenetic combination, and their formation pressure are strongly dependent on the physical and textural properties of the impacted quartz-bearing target. Porosity [13] and preshock temperature [9,12,14] are most effective. Both properties are lowering the threshold pressure for certain shock effects and they affect the orientation and type of planar deformation structures (PFs and PDFs). Upon thermometamorphism shocked quartz displays characteristic annealing effects useful for (limited) geothermometry. PDFs transform to "decorated planar features" due to recrystallization. These features persist up to the conditions of recrystallization of the primary quartz. Annealing of diaplectic glass leads to densification of the glass between 700 and 1200 degrees C and to complete recrystallization to alpha-quartz + alpha-cristobalite above 1200 degrees C [10]. In impact craters this transformation produces the characteristic "ballen" texture as observed in clasts of melt rocks. Stishovite and coesite decompose near 350 degrees C and above about 1150 degrees C, respectively. These annealing features provide important boundary conditions for interpreting the temperature-time history of impact formations. There is unequivocal evidence, strongly supported by TEM studies [3,4,8], that most of the shock effects discussed above and, certainly, the complete set cannot be produced by endogenic processes in near-surface environments of the Earth's crust where the strain rates are several orders of magnitude lower than those in impact processes, and the peak pressures exceed 5 GPa only in very special tectonic settings at great depth. References: [1] Stoffler D. (1972) Fortschr. Mineral., 49, 50-113, and references therein. [2] Stoffler D. (1974) Fortschr. Mineral., 51, 256-289. [3] Gratz A. J. et al. (1988) Phys. Chem. Mineral., 16, 221-233. [4] Goltrant O. et al. (1991) EPSL 106, 103-115. [5] Cygan R. T. et al. (1990) LPSC XX, 451-457. [6] Jakubith M. and Lehmann G. (1981) Phys. Chem. Mineral., 7, 165- 168. [7] Ashworth J. R. and Schneider H. (1985) Phys. Chem. Mineral., 11, 241- 249. [8] Stoffler D. (1984) J. Non-Cryst. Solids, 67, 465-502, and references therein. [9] Gratz A. J. (1992) Phys. Chem. Mineral., 19, 267-288, [10] Rehfeldt-Oskierski A. (1986) Ph.D. thesis, Univ. of Munster. [11] Grothues J. (1988) Diploma thesis, Univ. of Muenster [12] Langenhorst F. (1993), Ph.D. thesis, Univ. of Munster. [13] Kieffer S. W. et al. (1976) Contr. Mineral. Petrol., 59, 41-93, [14] Langenhorst F. (1992) Nature, 356, 507-509.
Pressure Induced Phase Transformations of Silica Polymorphs and Glasses
NASA Astrophysics Data System (ADS)
Cagin, Tahir; Demiralp, Ersan; Goddard, William A., III
1998-03-01
Silica, SiO_2, is one of the most widely studied substance, and it has some complex and unusual properties. We have used a recently developed 2-body interaction force field (E. Demiralp, T. Cagin, W.A. Goddard, III, unpublished.) to study the structural phase transformations in silica under various pressure loading conditions. The specific transformations we studied are α-quartz to stishovite, coesite to stishovite and fused glass to stishovite-like dense, a dominantly six-coordinated glassy phase. Molecular dynamics simulations are performed under the constant loading rates ranging from 0.1 GPa/ps to 2.0 GPa/ps, pressures upto 100 GPa and at temperatures 300, 500, 700 and 900 K. We observe the crystal to crystal transformations to occur reconstructively, whereas it occurs in a smooth and displacive manner from glass to a stishovite-like phase confirming earlier conjectures. (E.M. Stolper and T.J. Ahrens, Geophys. Res. Let.) 14, 1231 (1987). To elucidate the shock loading experiments, we studied the dependence of transition pressure on the loading rate and the temperature. To assess the hysterisis effect we also studied the unloading behavior of each transformation.
A New Multiphase Equation of State for SiO 2
DOE Office of Scientific and Technical Information (OSTI.GOV)
Maerzke, Katie A.; Gammel, J. Tinka
SiO 2 is found as α-quartz at ambient conditions. Under shock compression, it transforms into a much higher density stishovite-like phase around 20 GPa, then into a liquid phase above 100 GPa. The SESAME library contains older equations of state for α-quartz, polycrystalline quartz, and fused quartz. These equations of state model the material as a single phase; i.e., there is no high pressure phase transition. Somewhat more recently (in 1992), Jon Boettger published equations of state for α-quartz, coesite, and stishovite, along with a phase transition model to mix them. However, we do not have a multiphase EOS thatmore » captures the phase transitions in this material. Others are working on a high-accuracy model for very high pressure SiO 2, since liquid quartz is used as an impedance matching standard above 100 GPa; however, we are focused on the 10-50 GPa range. This intermediate pressure range is most relevant for modeling the decomposition products of silicone polymers such as Sylgard 184 and SX358.« less
Photoconductivity of Macroporous and Nonporous Silicon with Ultrathin Oxide Layers
NASA Astrophysics Data System (ADS)
Konin, K. P.; Goltvyansky, Yu. V.; Karachevtseva, L. A.; Karas, M. I.; Morozovs'ka, D. V.
2018-06-01
The photoconductivity of macroporous silicon with ultrathin oxide layers of 2.7-30 nm in thickness at short-wave optical excitation was studied. The following feature was revealed: a nonmonotonic change in the photoconductivity as a function of the oxide thickness. At a minimum thickness, the photoconductivity is negative; in the interval 6.8-15 nm, it is very much suppressed; at 15-30 nm, it is positive. Suppression of photoconductivity over a wide thickness range indicates an abnormally high concentration of traps and capture centers for charge carriers of both signs. Such a change in the photoconductivity corresponds to the known results on the continuous morphological rearrangement of the oxide in the thickness range from 6-7 nm to 12-15 nm from the coesite-like (4-membered SiO4 tetrahedra rings) to the tridymite-like (6-membered SiO4 tetrahedra rings). The suppression of photoconductivity in the intermediate range probably demonstrates the collective, antisynergetic action of these coexisting oxide forms on the nonequilibrium charge carriers. These coexisting oxide forms manifest themselves as an unusual collective defect.
Discovery of moganite in a lunar meteorite as a trace of H2O ice in the Moon’s regolith
Seto, Yusuke; Miyake, Akira; Sekine, Toshimori; Tomeoka, Kazushige; Matsumoto, Megumi; Kobayashi, Takamichi
2018-01-01
Moganite, a monoclinic SiO2 phase, has been discovered in a lunar meteorite. Silica micrograins occur as nanocrystalline aggregates of mostly moganite and occasionally coesite and stishovite in the KREEP (high potassium, rare-earth element, and phosphorus)–like gabbroic-basaltic breccia NWA 2727, although these grains are seemingly absent in other lunar meteorites. We interpret the origin of these grains as follows: alkaline water delivery to the Moon via carbonaceous chondrite collisions, fluid capture during impact-induced brecciation, moganite precipitation from the captured H2O at pH 9.5 to 10.5 and 363 to 399 K on the sunlit surface, and meteorite launch from the Moon caused by an impact at 8 to 22 GPa and >673 K. On the subsurface, this captured H2O may still remain as ice at estimated bulk content of >0.6 weight %. This indicates the possibility of the presence of abundant available water resources underneath local sites of the host bodies within the Procellarum KREEP and South Pole Aitken terranes. PMID:29732406
Diamonds in ophiolitic mantle rocks and podiform chromitites: An unsolved mystery
NASA Astrophysics Data System (ADS)
Yang, J.; Zhang, Z.; Xu, X.; Ba, D.; Bai, W.; Fabg, Q.; Meng, F.; Chen, S.; Robinson, P. T.; Dobrzhinetskaya, L.
2009-05-01
In recent years ultrahigh pressure minerals, such as diamond and coesite, and other unusual minerals were discovered in chromitites of the Luobusa ophiolite in Tibet, and 4 new minerals have been approved by the CNMMN. These results have raised many questionsWhat are the occurrences of the diamonds, what is the source of their carbon and how were they formed? What is the origin of the chromites hosting the diamonds and at what depth did they form? What is the genetic relationship between the diamonds and the host chromitites? In what geological, geophysical and geochemical environments can the diamonds be formed and how are they preserved? The UHP minerals from Luobusa are controversial because they have not been found in situ and because ophiolites are currently believed to form at shallow levels above oceanic spreading centers in suprasubduction zone environments. More detailed study and experimental work are needed to understand the origin and significance of these unusual minerals and investigations of other ophiolites are needed to determine if such minerals occur elsewhere To approach these problems, we have collected two one-ton samples of harzburgite hosting chromitite orebodies in the Luobusa ophiolite in Tibet. The harzburgite samples were taken close to chromitite orebody 31, from which the diamonds, coesite and other unusual minerals were recovered. We processed these two samples in the same manner as the chromitites and discovered numerous diamonds and more than 50 other mineral species. These preliminary results show that the minerals in the harzburgites are similar to those in the chromitites, suggesting a genetic relationship between them. To determine if such UHP and unusual minerals occur elsewhere, we collected about 1.5 t of chromitite from two orebodies in an ultramafic body in the Polar Urals. Thus far, more than 60 different mineral species have been separated from these ores. The most exciting discovery is the common occurrence of diamond, a typical UHP mineral in the Luobusa chromitites. Other minerals include: (1) native elements: Cr, W, Ni, Co, Si, Al and Ta; (2) carbides: SiC and WC; (3) alloys: Cr-Fe, Si-Al-Fe, Ni-Cu, Ag-Au, Ag-Sn, Fe-Si, Fe-P, and Ag-Zn-Sn; (4) oxides: NiCrFe, PbSn, REE, rutile and Si-bearing rutile, ilmenite, corundum, chromite, MgO, and SnO2; (5) silicates: kyanite, pseudomorphs of octahedral olivine, zircon, garnet, feldspar, and quartz,; (6) sulfides of Fe, Ni, Cu, Mo, Pb, Ab, AsFe, FeNi, CuZn, and CoFeNi; and (7) iron groups: native Fe, FeO, and Fe2O3. These minerals are very similar in composition and structure to those reported from the Luobusa chromitites.
NASA Astrophysics Data System (ADS)
Lang, H. M.; Gilotti, J. A.
2005-12-01
Although paragneiss is not common in the North-East Greenland Eclogite Province (NEGEP), of the few paragneiss samples collected in the UHP zone, some contain inclusion-rich garnet megacrysts (to 2 cm) in an anatectic matrix. In the matrix, quartz ribbons are segregated from anatectic melt layers and lenses that contain plagioclase, antiperthitic alkali-feldspar, white mica, biotite, small garnets, rutile and minor kyanite. In addition to one-phase and two-phase inclusions of quartz, polycrystalline quartz (no definitive coesite-replacement textures), and phengitic white mica, the garnet megacrysts contain some relatively large polyphase inclusions with all or most of the following phases: kyanite, rutile, phengitic white mica, biotite, quartz, Na-rich plagioclase, K-feldspar and zircon. Textures in these complex, polyphase inclusions suggest that their constituent minerals crystallized from a melt. Crystals are randomly oriented with early crystallizing minerals (kyanite, rutile, micas) forming euhedral grains and later crystallizing minerals (quartz and feldspars) filling the interstitial spaces. The textures and mineral assemblages are consistent with dehydration melting of phengitic white mica + quartz (enclosed in garnet) during decompression of the rocks from UHP metamorphic conditions. Although anatectic minerals in the matrix may have experienced extensive retrograde re-equilibration subsequent to crystallizing from a melt, the minerals trapped in the crystallized melt inclusions in garnet are likely to preserve their original textures and compositions. Microtextures in the melt inclusions and surrounding garnet suggest that partial melting was accompanied by volume expansion and that some melt penetrated garnets. Some radial fractures extend from inclusion margins into surrounding garnet. Individual fractures may have formed by volume expansion on melting or expansion accompanying the coesite-quartz transformation. Small and large polycrystalline quartz inclusions are commonly rimmed by a moat of plagioclase + K-feldspar, which extends into apophyses in garnet. These feldspar rims indicate that the most mobile and volatile-rich portion of the melt was able to penetrate garnets and travel along garnet-inclusion boundaries. Possible melt inclusions have been described in natural garnets from other UHP terranes (Stockert, et al., 2001, Geology; Hwang, et al., 2001, Earth and Planetary Science Letters) and have been produced experimentally (Perchuk, et al., 2005, Terra Nova). In the experiments and at least one of the natural occurrences, patchy microstructures (attributed to high Ca) were observed in BSE images of garnet surrounding the melt inclusions. Although we observe no garnet zoning in BSE images, patchy high-Ca zoning is apparent on X-ray maps of garnet surrounding the melt inclusions in our samples. Small, euhedral, high-Ca garnets are abundant in melt lenses in the matrix, so crystallization or recrystallization of high-Ca garnet surrounding the melt inclusions is not surprising.
Can Nitrogen be a Candidate for the Fe-Core Formation?
NASA Astrophysics Data System (ADS)
Dobrzhinetskaya, L.; Wirth, R.; Yang, J.; Weber, P.; Hutcheon, I.; Green, H. W.
2008-12-01
Among the light elements that have been added to mineral physics experiments concerning the Fe-rich core of the Earth, nitrogen is less favorable. In general, this is because metal-nitrides are thought to be rare within Earth. However this may not be because they are rare, but because nitrogen is difficult to detect by conventional electron microprobe analysis unless one is specifically looking for it. Theoretically, metal-nitrides could be equally considered as potential candidates for the light element in the core, not only because nitrogen forms strong metallic bonds, but also because metal-nitrides are common constituents of many iron meteorites. Some Fe-nitrides are found to be stable at extreme pressures and temperatures corresponding to Earth's core in both diamond anvil cell and shock experiments (Adler and Williams, 2005; Sekine et al., 2007). We have discovered a metal-nitride phase, TiN (osbornite) within a mantle mineralogical assemblage, opening a new opportunity to understand the history of Earth's core formation. The TiN was found in the mantle section of an unmetamorphosed Tibetan ophiolite, a fragment of former mid-ocean spreading center, which now marks the tectonic boundary between Asia and India. The osbornite occurs as inclusions in coesite pseudomorphic after stishovite, in association with FeTi alloy, native Fe, TiO2 II, cubic BN and diamond included in Os-Ir alloy, all from a massive chromitite ore body enclosed within harzburgite (Yang et al., 2007; Dobrzhinetskaya et al., 2007). The chromite also exhibits coesite and diopside exsolution lamellae (Yamamoto et al., 2007) that might suggest the calcium-ferrite polymorph of chromite as a precursor decompressed during upwelling. Measurements of δ15N with a Cameca 50 NanoSIMS using the same Focused Ion Beam foils prepared and used for earlier TEM studies suggest that the Tibetan osbornite is characterized by negative δ15N (-10 ‰). The δ15N results from the Tibetan osbornite are somewhat more negative than the most commonly measured value for Earth's uppermost mantle (δ15N = -3 to -5 ‰), and they are clearly different from the δ15N of shallow reservoirs. The latter include atmosphere, ocean, and crust having values of delta δ15N -- 0 - +5 ‰ for the atmosphere and ocean and +5 - +12 ‰.) for the crustal rocks and sediments. We conclude that the Tibetan osbornite contains mantle N, perhaps from an old and/or deep mantle reservoir. Apropos of the suggestion of N in the core, we point out that most iron meteorites have extremely negative δ15N values of -60 ‰ or more, hence it is conceivable that part of the N signal in our materials comes from a leaky core.
X-ray Raman scattering for structural investigation of silica/silicate minerals
NASA Astrophysics Data System (ADS)
Fukui, H.; Kanzaki, M.; Hiraoka, N.; Cai, Y. Q.
2009-03-01
We have performed X-ray Raman scattering (XRS) measurements on the oxygen K and silicon L absorption edges of four silica minerals: α-quartz, α-cristobalite, coesite, and stishovite. We have also calculated the partial electron densities of states (DOSs) and compared these with the XRS spectra. This study demonstrates that the short-range structure around the atom of interest strongly influences the XRS spectral features. Importantly, the oxygen K-edge XRS spectra are found to reflect the p-orbital DOS while the silicon L-edge spectra reflect the s- and d-orbital DOSs, even when a product of a momentum transfer and a mean radius of a electron orbit (1 s for oxygen and 2 p for silicon), Qr, is close to or larger than unity. Building on this, calculations of the partial DOSs for other silica phases are presented, including ultra-high-pressure phases, which provide a good reference for further XRS study of silica and silicate minerals. XRS measurements should be performed on not only either of oxygen or silicon but also on many kinds of constituent elements to reveal the structural change of glasses/melts of silicates under extreme conditions.
Synchrotron radiation study on the phase relations of KAlSi3O8
NASA Astrophysics Data System (ADS)
Urakawa, Satoru; Ohno, Hideo; Igawa, Naoki; Kondo, Tadashi; Shimomura, Osamu
1994-07-01
The equilibrium phase relations of KAlSi3O8 have been determined by in situ X-ray diffraction method using synchrotron radiation at Photon Factory, Natl. Lab. for High Energy Physics. Experiments were conducted by using the cubic type high pressure apparatus, MAX90, equipped with sintered diamond anvils. The temperature region was extended to 2000 °C up to 10 GPa in this study. Sanidine, the low pressure phase of KAlSi3O8, decomposes into three phases, the wadeite-type K2Si4O9+kyanite (Al2SiO5)+coesite (SiO2), at 6.5 GPa and 1200˜1300 °C. The hollandite-type KAlSi3O8 is made up of three phases at 9.2 GPa and 1300˜1400 °C. The melting points of sanidine and the hollandite-type KAlSi3O8 are 1600 °C at 6.7 GPa and 1800 °C at 11.2 GPa, respectively. In three phases coexisting field, wadeite-type K2Si4O9 first melts at the temperature between 1400 °C and 1500 °C.
Synchrotron radiation study on the high-pressure and high-temperature phase relations of KAlSi3O8
NASA Astrophysics Data System (ADS)
Urakawa, S.; Kondo, T.; Igawa, N.; Shimomura, O.; Ohno, H.
1994-10-01
In situ X-ray diffraction study on KAlSi3O8 has been performed using the cubic type high pressure apparatus, MAX90, combined with synchrotron radiation. We determined the phase relations of sanidine, the wadeite-type K2Si4O9+kyanite (Al2SiO5)+coesite (SiO2) assemblage, and hollandite-type KAlSi3O8, including melting temperatures of potassic phases, up to 11 GPa. Our data on subsolidus phase boundaries are close to the recent data of Yagi and Akaogi (1991). Melting relations of sanidine are consistent with the low pressure data of Lindsley (1966). The breakdown of sanidine into three phases reduces melting temperature, and wadeite-type K2Si4O9 melts first around 1500° C in three phase coexisting region. Melting point of hollandite-type KAlSi3O8 is between 1700° C and 1800° C at 11 GPa. If these potassic phases host potassium in the earth's mantle, the true mantle solidus temperature will be much lower than the reported dry solidus temperature of peridotite.
High-pressure minerals in eucrite suggest a small source crater on Vesta
Pang, Run-Lian; Zhang, Ai-Cheng; Wang, Shu-Zhou; Wang, Ru-Cheng; Yurimoto, Hisayoshi
2016-01-01
High-pressure minerals in meteorites are important records of shock events that have affected the surfaces of planets and asteroids. A widespread distribution of impact craters has been observed on the Vestan surface. However, very few high-pressure minerals have been discovered in Howardite-Eucrite-Diogenite (HED) meteorites. Here we present the first evidence of tissintite, vacancy-rich clinopyroxene, and super-silicic garnet in the eucrite Northwest Africa (NWA) 8003. Combined with coesite and stishovite, the presence of these high-pressure minerals and their chemical compositions reveal that solidification of melt veins in NWA 8003 began at a pressure of >~10 GPa and ceased when the pressure dropped to <~8.5 GPa. The shock temperature in the melt veins exceeded 1900 °C. Simulation results show that shock events that create impact craters of ~3 km in diameter (subject to a factor of 2 uncertainty) are associated with sufficiently high pressures to account for the occurrence of the high-pressure minerals observed in NWA 8003. This indicates that HED meteorites containing similar high-pressure minerals should be observed more frequently than previously thought. PMID:27181381
Mattinson, C.G.; Wooden, J.L.; Liou, J.G.; Bird, D.K.; Wu, C.L.
2006-01-01
Amphibolite-facies para- and orthogneisses near Dulan, in the southeast part of the North Qaidam terrane, enclose minor ultra-high pressure (UHP) eclogite and peridotite. Field relations and coesite inclusions in zircons from paragneiss suggest that felsic, mafic, and ultramafic rocks all experienced UHP metamorphism and a common amphibolite-facies retrogression. Ion microprobe U-Pb and REE analyses of zircons from two granitic orthogneisses indicate magmatic crystallization at 927 ?? Ma and 921 ?? 7 Ma. Zircon rims in one of these samples yield younger ages (397-618 Ma) compatible with partial zircon recrystallization during in-situ Ordovician-Silurian eclogite-facies metamorphism previously determined from eclogite and paragneiss in this area. The similarity between a 2496 ?? 18 Ma xenocrystic core and 2.4-2.5 Ga zircon cores in the surrounding paragneiss suggests that the granites intruded the sediments or that the granite is a melt of the older basement which supplied detritus to the sediments. The magmatic ages of the granitic orthogneisses are similar to 920-930 Ma ages of (meta)granitoids described further northwest in the North Qaidam terrane and its correlative west of the Altyn Tagh fault, suggesting that these areas formed a coherent block prior to widespread Mid Proterozoic granitic magmatism. ?? Springer-Verlag 2006.
IR calibrations for water determination in olivine, r-GeO2, and SiO2 polymorphs
NASA Astrophysics Data System (ADS)
Thomas, Sylvia-Monique; Koch-Müller, Monika; Reichart, Patrick; Rhede, Dieter; Thomas, Rainer; Wirth, Richard; Matsyuk, Stanislav
2009-10-01
Mineral-specific IR absorption coefficients were calculated for natural and synthetic olivine, SiO2 polymorphs, and GeO2 with specific isolated OH point defects using quantitative data from independent techniques such as proton-proton scattering, confocal Raman spectroscopy, and secondary ion mass spectrometry. Moreover, we present a routine to detect OH traces in anisotropic minerals using Raman spectroscopy combined with the “Comparator Technique”. In case of olivine and the SiO2 system, it turns out that the magnitude of ɛ for one structure is independent of the type of OH point defect and therewith the peak position (quartz ɛ = 89,000 ± 15,000 text{l} text{mol}_{{text{H}_2}text{O}}^{-1} text{cm}^{-2}), but it varies as a function of structure (coesite ɛ = 214,000 ± 14,000 text{l} text{mol}_{{text{H}_2}text{O}}^{-1} text{cm}^{-2}; stishovite ɛ = 485,000 ± 109,000 text{l} text{mol}_{{text{H}_2}text{O}}^{-1} text{cm}^{-2}). Evaluation of data from this study confirms that not using mineral-specific IR calibrations for the OH quantification in nominally anhydrous minerals leads to inaccurate estimations of OH concentrations, which constitute the basis for modeling the Earth’s deep water cycle.
Eclogites and their geodynamic interpretation: a history
NASA Astrophysics Data System (ADS)
Godard, Gaston
2001-09-01
Haüy coined the term eclogite, meaning "chosen rock", in 1822, but de Saussure had already observed rocks of this type in the Alps four decades earlier. Throughout the 19th century, the origin of eclogite remained an enigma, in spite of great progress in our knowledge of this rock. The first chemical analyses, carried out around 1870, showed that its bulk composition was the same as gabbro. Therefore, eclogite was thought to be either an igneous rock of gabbroic composition or a metamorphosed gabbro. This second hypothesis became preferred when progressive transitions were observed between gabbros and eclogites. In 1903, simply by comparing the molar volumes of gabbroic and eclogite parageneses, Becke inferred that eclogite was the high-pressure equivalent of gabbro. In 1920, eclogite was involved in the conception of the metamorphic facies by Eskola. However, a few researchers denied the existence of an eclogite facies, and claimed that high stress instead of high lithostatic pressure could generate eclogites. In the 1960s, consideration of the water pressure parameter also favoured the belief that eclogite was simply the anhydrous equivalent of amphibolite. Finally, eclogite was definitely considered as a high-pressure metamorphic rock following the development of experimental petrology and the application of thermodynamics. In recent years, the discovery of ultrahigh-pressure coesite-bearing rocks in the crust has drastically changed geologists' ideas concerning the limits of eclogite-facies crustal metamorphism. Eclogites have been involved in several geodynamic theories. Around 1900, kimberlite studies favoured the idea that eclogite might be abundant in the interior of the Earth. In 1912, Fermor predicted the existence of a dense eclogite-bearing zone in the mantle. This "eclogite layer" hypothesis was still envisaged as late as 1970. The alternative "peridotite" hypothesis became preferred when experimental investigations demonstrated that the gabbro-to-eclogite transition could not coincide with a sharp Mohorovičić discontinuity. Before plate tectonics, high-pressure belts were interpreted as remnants of ophiolite-bearing "geosynclines", metamorphosed by loading during thrust faulting. After the acceptance of plate tectonics, around 1970, the same high-pressure Alpine-type belts came to be considered as former oceanic crust, transformed into eclogite within subduction zones, and subsequently incorporated into mountain belts. Surprisingly, formation of eclogite in "subsidence" zones (i.e. subduction zones) had already been envisaged as early as 1931 by Holmes, the inventor of a convection-current theory. In the 1980s, many authors tried to apply the model of Alpine-type high-pressure belts to eclogites enclosed within the gneisses of ancient orogens, but the question remains obscure nowadays. These eclogites have been involved in the "in situ versus foreign" controversy and in the unresolved enigma of ultrahigh-pressure metamorphism. The latter came under scrutiny in 1984 after the discovery of coesite and diamond in some eclogite-facies rocks. It has been a matter of considerable interest during the last two decades. Currently, the debate is focused on the geodynamic mechanisms responsible for the exhumation of these rocks, a question that will probably remain unresolved for part of the coming century.
NASA Astrophysics Data System (ADS)
Wang, L.; Kusky, T.
2009-12-01
High-precision 1:1,000 mapping of Yangkou Bay, eastern Sulu orogen, defines the structural geometry and history of the world’s most significant UHP (Ultrahigh Pressure) rock exposures. Four stages of folds are recognized in the UHP rocks and associated quartzo-feldspathic gneiss. Eclogite facies rootless F1 and isoclinal F2 folds are preserved locally in coesite-eclogite. Mylonitic to ultramylonitic cosesit-eclogite shear zones separate 5-10-meter-thick nappes of ultramafic-mafic UHP rocks from banded quartzo-feldspathic gneiss. These shear zones are folded, and progressively overprinted by amphibolite and greenschist facies shear zones that become wider with lower grade. The deformation sequences is explained by deep subduction of offscraped thrust slices of oceanic or lower continental crust, caught between the colliding North and South China cratons in the Mesozoic. After these slices were structurally isolated along the plate interface, they were rolled like ball-bearings, in the subduction channel during their exhumation, forming several generations of folds, sequentially lower-grade foliations and lineations, and intruded by several generations of in situ and exotically derived melts. The shear zones formed during different generations of deformation are wider with lower grades, suggesting that deep-crustal/upper mantle deformation operates efficiently (perhaps with more active crystallographic slip systems) than deformation at mid to upper crustal levels.
Evidence of Former Stishovite in Metamorphosed Sediments: Exhumation from >300 km
NASA Astrophysics Data System (ADS)
Liu, L.; Zhang, J.; Green, H. W.; Jin, Z.
2005-12-01
Deep subduction of continental rocks or sediments is difficult because they are buoyant relative to mantle compositions. Nevertheless, it has been shown that during continental collision, such rocks can be subducted to ~200km and returned to the surface. At pressures equivalent to ~300 km, experimental studies indicate that continental rocks will become more dense than ambient mantle and therefore presumably lose their ability to return to the surface buoyantly. We have discovered distinctive aluminum- and iron-bearing oxide inclusions (oriented kyanite and hercynite) in quartz of high-pressure pelitic rocks from the Altyn Tagh, western China that may represent rocks subducted to approximately this point of no return. The inclusions exhibit all of the characteristics of phases exsolved from solid solution except that they have no topotaxy with their host quartz; in many cases, the oriented inclusions cross high-angle quartz grain boundaries with no deviation in their orientations. The abundance of these phases (~1 vol%) is also incompatible with the known solubility of Fe and Al in either quartz or coesite. We have performed laboratory experiments at high pressure and found that these observations are consistent with the possibility that the oxides precipitated from stishovite, which is stable only above ~10GPa. These observations strongly suggest that these pelitic (clay-rich) sediments have been subducted to at least 300 km and returned to the surface.
Proterozoic Bushveld-Vredefort catastrophe: Possible causes and consequences
NASA Technical Reports Server (NTRS)
Elston, W. E.; Twist, D.
1988-01-01
Bushveld Complex and Vredefort Dome are unique features, formed in close proximity during the same time interval, approximately 2 Ga. Both show evidence of catastrophic events in the shallow marine environment of the otherwise stable Kaapvaal Craton. Explanation by multiple impacts of an asteroid, brecciated by an inter-asteroidal collision and disintegrating in Earth's gravity field is supported by pseudotachylite, shatter cones, coesite, and stishovite at Vredefort but these shock phenomena were not found in the Bushveld Complex. The Bushveld Complex was formerly interpreted as a lopolith, a view incompatible with gravity, electrical resistivity, magnetic, and seismic-reflection data. It is outlined by five inward-dipping lobes of layered ultramafic-mafic plutonic rocks that partly coalesce to form a basin-like feature 400 km in diameter and 65,000 sq. km. in area, equivalent to a small lunar mare. The Bushveld Complex is orders of magnitudes larger than other proposed terrestrial impact structures and differs from them in important ways. Its principal members, in order of age, are Rooiberg Felsite, RLS, and Lebowa Granite. The Bushveld-Vredefort events occurred during the interval from neutral or reducing atmosphere to oxidizing atmosphere. This transition is usually related to the evolution of photosynthesizing organisms. If the impact hypothesis for Bushveld-Vredefort can be confirmed, it may represent a global catastrophe sufficient to contribute to environmental changes favoring aerobic photosynthesizing eukaryotes over anaerobic prokaryotes.
Reduced sediment melting at 7.5-12 GPa: phase relations, geochemical signals and diamond nucleation
NASA Astrophysics Data System (ADS)
Brey, G. P.; Girnis, A. V.; Bulatov, V. K.; Höfer, H. E.; Gerdes, A.; Woodland, A. B.
2015-08-01
Melting of carbonated sediment in the presence of graphite or diamond was experimentally investigated at 7.5-12 GPa and 800-1600 °C in a multianvil apparatus. Two starting materials similar to GLOSS of Plank and Langmuir (Chem Geol 145:325-394, 1998) were prepared from oxides, carbonates, hydroxides and graphite. One mixture (Na-gloss) was identical in major element composition to GLOSS, and the other was poorer in Na and richer in K (K-gloss). Both starting mixtures contained ~6 wt% CO2 and 7 wt% H2O and were doped at a ~100 ppm level with a number of trace elements, including REE, LILE and HFSE. The near-solidus mineral assemblage contained a silica polymorph (coesite or stishovite), garnet, kyanite, clinopyroxene, carbonates (aragonite and magnesite-siderite solid solution), zircon, rutile, bearthite and hydrous phases (phengite and lawsonite at <9 GPa and the hydrous aluminosilicates topaz-OH and phase egg at >10 GPa). Hydrous phases disappear at ~900 °C, and carbonates persist up to 1000-1100 °C. At temperatures >1200 °C, the mineral assemblage consists of coesite or stishovite, kyanite and garnet. Clinopyroxene stability depends strongly on the Na content in the starting mixture; it remains in the Na-gloss composition up to 1600 °C at 12 GPa, but was not observed in K-gloss experiments above 1200 °C. The composition of melt or fluid changes gradually with increasing temperature from hydrous carbonate-rich (<10 wt% SiO2) at 800-1000 °C to volatile-rich silicate liquids (up to 40 wt% SiO2) at high temperatures. Trace elements were analyzed in melts and crystalline phases by LA ICP MS. The garnet-melt and clinopyroxene-melt partition coefficients are in general consistent with results from the literature for volatile-free systems and silicocarbonate melts derived by melting carbonated peridotites. Most trace elements are strongly incompatible in kyanite and silica polymorphs ( D < 0.01), except for V, Cr and Ni, which are slightly compatible in kyanite ( D > 1). Aragonite and Fe-Mg carbonate have very different REE partition coefficients ( D Mst-Sd/L ~ 0.01 and D Arg/L ~ 1). Nb, Ta, Zr and Hf are strongly incompatible in both carbonates. The bearthite/melt partition coefficients are very high for LREE (>10) and decrease to ~1 for HREE. All HFSE are strongly incompatible in bearthite. In contrast, Ta, Nb, Zr and Hf are moderately to strongly compatible in ZrSiO4 and TiO2 phases. Based on the obtained partition coefficients, the composition of a mobile phase derived by sediment melting in deep subduction zones was calculated. This phase is strongly enriched in incompatible elements and displays a pronounced negative Ta-Nb anomaly but no Zr-Hf anomaly. Although all experiments were conducted in the diamond stability field, only graphite was observed in low-temperature experiments. Spontaneous diamond nucleation and the complete transformation of graphite to diamond were observed at temperatures above 1200-1300 °C. We speculate that the observed character of graphite-diamond transformation is controlled by relationships between the kinetics of metastable graphite dissolution and diamond nucleation in a hydrous silicocarbonate melt that is oversaturated in C.
The relationship between mantle pH and the deep nitrogen cycle
NASA Astrophysics Data System (ADS)
Mikhail, Sami; Barry, Peter H.; Sverjensky, Dimitri A.
2017-07-01
Nitrogen is distributed throughout all terrestrial geological reservoirs (i.e., the crust, mantle, and core), which are in a constant state of disequilibrium due to metabolic factors at Earth's surface, chemical weathering, diffusion, and deep N fluxes imposed by plate tectonics. However, the behavior of nitrogen during subduction is the subject of ongoing debate. There is a general consensus that during the crystallization of minerals from melts, monatomic nitrogen behaves like argon (highly incompatible) and ammonium behaves like potassium and rubidium (which are relatively less incompatible). Therefore, the behavior of nitrogen is fundamentally underpinned by its chemical speciation. In aqueous fluids, the controlling factor which determines if nitrogen is molecular (N2) or ammonic (inclusive of both NH4+ and NH30) is oxygen fugacity, whereas pH designates if ammonic nitrogen is NH4+ or NH30. Therefore, to address the speciation of nitrogen at high pressures and temperatures, one must also consider pH at the respective pressure-temperature conditions. To accomplish this goal we have used the Deep Earth Water Model (DEW) to calculate the activities of aqueous nitrogen from 1-5 GPa and 600-1000 °C in equilibrium with a model eclogite-facies mineral assemblage of jadeite + kyanite + quartz/coesite (metasediment), jadeite + pyrope + talc + quartz/coesite (metamorphosed mafic rocks), and carbonaceous eclogite (metamorphosed mafic rocks + elemental carbon). We then compare these data with previously published data for the speciation of aqueous nitrogen across these respective P-T conditions in equilibrium with a model peridotite mineral assemblage (Mikhail and Sverjensky, 2014). In addition, we have carried out full aqueous speciation and solubility calculations for the more complex fluids in equilibrium with jadeite + pyrope + kyanite + diamond, and for fluids in equilibrium with forsterite + enstatite + pyrope + diamond. Our results show that the pH of the fluid is controlled by mineralogy for a given pressure and temperature, and that pH can vary by several units in the pressure-temperature range of 1-5 GPa and 600-1000 °C. Our data show that increasing temperature stabilizes molecular nitrogen and increasing pressure stabilizes ammonic nitrogen. Our model also predicts a stark difference for the dominance of ammonic vs. molecular and ammonium vs. ammonia for aqueous nitrogen in equilibrium with eclogite-facies and peridotite mineralogies, and as a function of the total dissolved nitrogen in the aqueous fluid where lower N concentrations favor aqueous ammonic nitrogen stabilization and higher N concentrations favor aqueous N2. Overall, we present thermodynamic evidence for nitrogen to be reconsidered as an extremely dynamic (chameleon) element whose speciation and therefore behavior is determined by a combination of temperature, pressure, oxygen fugacity, chemical activity, and pH. We show that altering the mineralogy in equilibrium with the fluid can lead to a pH shift of up to 4 units at 5 GPa and 1000 °C. Therefore, we conclude that pH imparts a strong control on nitrogen speciation, and thus N flux, and should be considered a significant factor in high temperature geochemical modeling in the future. Finally, our modelling demonstrates that pH plays an important role in controlling speciation, and thus mass transport, of Eh-pH sensitive elements at temperatures up to at least 1000 °C.
NASA Astrophysics Data System (ADS)
Ferrero, Silvio; O'Brien, Patrick; Walczak, Katarzyna; Wunder, Bernd; Hecht, Lutz
2014-05-01
Melt inclusions (MI) study in migmatites is a powerful tool to retrieve the original composition of the anatectic melt, both as major elements (Ferrero et al., 2012) and fluid contents (Bartoli et al., 2013). Crystallized MI, or "nanogranites" (Cesare et al., 2009), were identified within HP felsic granulites from Orlica-Śnieżnik Dome, NE Bohemian Massif (Walczak, 2011). The investigated samples are Grt+Ky leucogranulites originated from a granitic protolith, with assemblage Qtz+Pl+Kfs+Grt+Ky+Ttn+Rt+Ilm. Nanogranites occur in garnet as primary inclusions, and consist of Qtz+Ab+Bt+Kfs±Ep±Ap. Such assemblage results from the crystallization of a melt generated during a partial melting reaction; the same reaction is also responsible for the production of the host garnet, interpreted therefore as a peritectic phase. Besides nanogranites, former presence of melt is supported by the occurrence of tiny pseudomorphs of melt-filled pores (Holness & Sawyer, 2008) and euhedral faces in garnet. Garnet composition, with Grs =0.28-0.31, phase assemblage (kyanite, ternary feldspar) and classic thermobarometry suggest that partial melting took place at T≥875°C and P~2.2-2.6 GPa, under eclogite-facies conditions. Although other authors reported palisade quartz after coesite in this area (see e.g. Bakun-Czubarow, 1992), no clear evidence of UHP conditions have been identified during this study. Piston cylinder re-homogenization experiments were performed on MI-bearing garnet chips to obtain the composition of the pristine anatectic melt. The first data from experiments in the range 850-950°C and 2-2.2 GPa show that nanogranites can be re-melted at T≥875°. However, homogenization has not been reached yet since new Grt, with lower CaO and higher MgO, crystallizes on the walls of the inclusion. As P increases, the modal amount of new phase decreases, while its composition evolves closer to those of the host garnet. Further experiments at higher pressure are in underway, with the aim to achieve full re-homogenization and reproduce the system garnet+melt present during anatexis. References Bakun-Czubarow, N., 1992. Quartz pseudomorphs after coesite and quartz exsolutions in eclogitic omphacites of the Zlote Mountains in the Sudetes, SW Poland. Archeological Mineralogy, 48, 3-25. Bartoli, O., Cesare, B., Poli, S., Bodnar, R.J., Acosta-Vigil, A., Frezzotti, M.L. & Meli, S., 2013. Recovering the composition of melt and the fluid regime at the onset of crustal anatexis and S-type granite formation. Geology, 41, 115-118. Cesare, B., Ferrero, S., Salvioli-Mariani, E., Pedron, D. & Cavallo, A., 2009. Nanogranite and glassy inclusions: the anatectic melt in migmatites and granulites. Geology, 37, 627-630. Ferrero, S., Bartoli, O., Cesare, B., Salvioli Mariani, E., Acosta-Vigil, A., Cavallo, A., Groppo, C. & Battiston, S., 2012. Microstructures of melt inclusions in anatectic metasedimentary rocks. Journal of Metamorphic Geology, 30, 303-322. Holness, M.B. & Sawyer, E.W., 2008. On the pseudomorphing of melt-filled pores during the crystallization of migmatites. Journal of Petrology, 49, 1343-1363. Walczak, K., 2011. "Interpretation of Sm-Nd and Lu-Hf dating of garnets from high pressure and high temperature rocks in the light of the trace elements distribution." Doctoral dissertation, Institute of Geological Sciences, Polish Academy of Sciences, Poland.
NASA Astrophysics Data System (ADS)
Liu, Fulai; Gerdes, Axel; Zeng, Lingsen; Xue, Huaimin
2008-06-01
In this study, we link mineral inclusion data, trace element analyses, U-Pb age and Hf isotope composition obtained from distinct zircon domains of complex zircon to unravel the origin and multi-stage metamorphic evolution of amphibolites from the Sulu ultrahigh-pressure (UHP) terrane, eastern China. Zircon grains separated from amphibolites from the CCSD-MH drill hole (G12) and Niushan outcrop (G13) were subdivided into two main types based on cathodoluminescence (CL) and Laser Raman spectroscopy: big dusty zircons with inherited cores and UHP metamorphic rims and small clear zircons. Weakly zoned, grey-white luminescent inherited cores preserve mineral inclusions of Cpx + Pl + Ap ± Qtz indicative of a mafic igneous protolith. Dark grey luminescent overgrowth rims contain the coesite eclogite-facies mineral inclusion assemblage Coe + Grt + Omp + Phe + Ap, and formed at T = 732-839 °C and P = 3.0-4.0 GPa. In contrast, white luminescent small clear zircons preserve mineral inclusions formed during retrograde HP quartz eclogite to LP amphibolite-facies metamorphism (T = 612-698 °C and P = 0.70-1.05 GPa). Inherited zircons from both samples yield SHRIMP 206Pb/238U ages of 695-520 Ma with an upper intercept age of 800 ± 31 Ma. The UHP rims yield consistent Triassic ages around 236-225 and 239-225 Ma for G12 and G13 with weighted means of 229 ± 3 and 231 ± 3 Ma, respectively. Small clear zircons from both samples give 206Pb/238U ages around 219-210 Ma with a weighted mean of 214 ± 3 Ma, interpreted as the age of retrograde quartz eclogite-facies metamorphism. Matrix amphibole from both samples indicate Ar-Ar ages of 209 ± 0.7 and 207 ± 0.7 Ma, respectively, probably dating late amphibolite-facies retrogression. The data suggest subduction of Neoproterozoic mafic igneous rocks to UHP conditions in Middle Triassic (∼230 Ma) times and subsequent exhumation to an early HP (∼214 Ma) and a late LP stage (∼208 Ma) over a period of ∼16 and 6 Myr, respectively. Thus, early exhumation from a mantle depth of 120-100 km to about 60 km occurred at an average rate of 0.3 cm/y, while subsequent exhumation to a middle crustal level took place at approximately 0.54 cm/y. These exhumation rates are considerably slower than those obtained for UHP rocks in the Dora Maira and Kokchetav massifs (2-3 cm/y). Based on similar P-T estimates and trace element and Hf isotope compositions, Sulu amphibolites can be identified as retrograde UHP eclogites. The εHf(800) of +8 implies a significant input from the depleted mantle to the Sulu-Dabie terrane during the middle Neoproterozoic. Overgrown rims are characterized by a distinct trace element composition with low Lu/Hf and Th/U and significantly higher 176Hf/177Hf ratios than inherited cores, consistent with formation during/after garnet (re-)crystallization and fractionation of the Lu-Hf system during UHP metamorphism. The combined dataset suggests homogenization of the 176Hf/177Hf ratio within the metamorphic mineral assemblage and during protolith formation. Observed variations are explained by mixing of material from both domains during laser ablation, e.g., due to partial recrystallization of inherited cores.
NASA Astrophysics Data System (ADS)
Fazio, Agnese; Folco, Luigi; D'Orazio, Massimo; Frezzotti, Maria Luce; Cordier, Carole
2014-12-01
Kamil is a 45 m diameter impact crater identified in 2008 in southern Egypt. It was generated by the hypervelocity impact of the Gebel Kamil iron meteorite on a sedimentary target, namely layered sandstones with subhorizontal bedding. We have carried out a petrographic study of samples from the crater wall and ejecta deposits collected during our first geophysical campaign (February 2010) in order to investigate shock effects recorded in these rocks. Ejecta samples reveal a wide range of shock features common in quartz-rich target rocks. They have been divided into two categories, as a function of their abundance at thin section scale: (1) pervasive shock features (the most abundant), including fracturing, planar deformation features, and impact melt lapilli and bombs, and (2) localized shock features (the least abundant) including high-pressure phases and localized impact melting in the form of intergranular melt, melt veins, and melt films in shatter cones. In particular, Kamil crater is the smallest impact crater where shatter cones, coesite, stishovite, diamond, and melt veins have been reported. Based on experimental calibrations reported in the literature, pervasive shock features suggest that the maximum shock pressure was between 30 and 60 GPa. Using the planar impact approximation, we calculate a vertical component of the impact velocity of at least 3.5 km s-1. The wide range of shock features and their freshness make Kamil a natural laboratory for studying impact cratering and shock deformation processes in small impact structures.
High-pressure synthesis of mesoporous stishovite: potential applications in mineral physics
NASA Astrophysics Data System (ADS)
Stagno, Vincenzo; Mandal, Manik; Landskron, Kai; Fei, Yingwei
2015-06-01
Recently, we have described a successful synthesis route to obtain mesoporous quartz and its high-pressure polymorph coesite by nanocasting at high pressure using periodic mesostructured precursors, such as SBA-16 and FDU-12/carbon composite as starting materials. Periodic mesoporous high-pressure silica polymorphs are of particular interest as they combine transport properties and physical properties such as hardness that potentially enable the industrial use of these materials. In addition, synthesis of mesoporous crystalline silica phases can allow more detailed geology-related studies such as water/mineral interaction, dissolution/crystallization rate and the surface contribution to the associated thermodynamic stability (free energy and enthalpy) of the various polymorphs and their crossover. Here, we present results of synthesis of mesoporous stishovite from cubic large-pore periodic mesoporous silica LP-FDU-12/C composite as precursor with an fcc lattice. We describe the synthesis procedure using multi-anvil apparatus at 9 GPa (about 90,000 atm) and temperature of 500 °C. The synthetic mesoporous stishovite is, then, characterized by wide and small-angle X-ray diffraction, scanning/transmission electron microscopy and gas adsorption. Results show that this new material is characterized by accessible mesopores with wide pore size distribution, surface area of ~45 m2/g and volume of pores of ~0.15 cm3/g. Results from gas adsorption indicate that both porosity and permeability are retained at the high pressures of synthesis but with weak periodic order of the pores.
Buoyancy-driven, rapid exhumation of ultrahigh-pressure metamorphosed continental crust.
Ernst, W G; Maruyama, S; Wallis, S
1997-09-02
Preservation of ultrahigh-pressure (UHP) minerals formed at depths of 90-125 km require unusual conditions. Our subduction model involves underflow of a salient (250 +/- 150 km wide, 90-125 km long) of continental crust embedded in cold, largely oceanic crust-capped lithosphere; loss of leading portions of the high-density oceanic lithosphere by slab break-off, as increasing volumes of microcontinental material enter the subduction zone; buoyancy-driven return toward midcrustal levels of a thin (2-15 km thick), low-density slice; finally, uplift, backfolding, normal faulting, and exposure of the UHP terrane. Sustained over approximately 20 million years, rapid ( approximately 5 mm/year) exhumation of the thin-aspect ratio UHP sialic sheet caught between cooler hanging-wall plate and refrigerating, downgoing lithosphere allows withdrawal of heat along both its upper and lower surfaces. The intracratonal position of most UHP complexes reflects consumption of an intervening ocean basin and introduction of a sialic promontory into the subduction zone. UHP metamorphic terranes consist chiefly of transformed, yet relatively low-density continental crust compared with displaced mantle material-otherwise such complexes could not return to shallow depths. Relatively rare metabasaltic, metagabbroic, and metacherty lithologies retain traces of phases characteristic of UHP conditions because they are massive, virtually impervious to fluids, and nearly anhydrous. In contrast, H2O-rich quartzofeldspathic, gneissose/schistose, more permeable metasedimentary and metagranitic units have backreacted thoroughly, so coesite and other UHP silicates are exceedingly rare. Because of the initial presence of biogenic carbon, and its especially sluggish transformation rate, UHP paragneisses contain the most abundantly preserved crustal diamonds.
Buoyancy-driven, rapid exhumation of ultrahigh-pressure metamorphosed continental crust
Ernst, W. G.; Maruyama, S.; Wallis, S.
1997-01-01
Preservation of ultrahigh-pressure (UHP) minerals formed at depths of 90–125 km require unusual conditions. Our subduction model involves underflow of a salient (250 ± 150 km wide, 90–125 km long) of continental crust embedded in cold, largely oceanic crust-capped lithosphere; loss of leading portions of the high-density oceanic lithosphere by slab break-off, as increasing volumes of microcontinental material enter the subduction zone; buoyancy-driven return toward midcrustal levels of a thin (2–15 km thick), low-density slice; finally, uplift, backfolding, normal faulting, and exposure of the UHP terrane. Sustained over ≈20 million years, rapid (≈5 mm/year) exhumation of the thin-aspect ratio UHP sialic sheet caught between cooler hanging-wall plate and refrigerating, downgoing lithosphere allows withdrawal of heat along both its upper and lower surfaces. The intracratonal position of most UHP complexes reflects consumption of an intervening ocean basin and introduction of a sialic promontory into the subduction zone. UHP metamorphic terranes consist chiefly of transformed, yet relatively low-density continental crust compared with displaced mantle material—otherwise such complexes could not return to shallow depths. Relatively rare metabasaltic, metagabbroic, and metacherty lithologies retain traces of phases characteristic of UHP conditions because they are massive, virtually impervious to fluids, and nearly anhydrous. In contrast, H2O-rich quartzofeldspathic, gneissose/schistose, more permeable metasedimentary and metagranitic units have backreacted thoroughly, so coesite and other UHP silicates are exceedingly rare. Because of the initial presence of biogenic carbon, and its especially sluggish transformation rate, UHP paragneisses contain the most abundantly preserved crustal diamonds. PMID:11038569
DOE Office of Scientific and Technical Information (OSTI.GOV)
Wang, Xuebing; Chen, Ting; Qi, Xintong
In this study, we developed a new method for in-situ pressure determination in multi-anvil, high-pressure apparatus using an acoustic travel time approach within the framework of acoustoelasticity. The ultrasonic travel times of polycrystalline Al{sub 2}O{sub 3} were calibrated against NaCl pressure scale up to 15 GPa and 900 °C in a Kawai-type double-stage multi-anvil apparatus in conjunction with synchrotron X-radiation, thereby providing a convenient and reliable gauge for pressure determination at ambient and high temperatures. The pressures derived from this new travel time method are in excellent agreement with those from the fixed-point methods. Application of this new pressure gauge in anmore » offline experiment revealed a remarkable agreement of the densities of coesite with those from the previous single crystal compression studies under hydrostatic conditions, thus providing strong validation for the current travel time pressure scale. The travel time approach not only can be used for continuous in-situ pressure determination at room temperature, high temperatures, during compression and decompression, but also bears a unique capability that none of the previous scales can deliver, i.e., simultaneous pressure and temperature determination with a high accuracy (±0.16 GPa in pressure and ±17 °C in temperature). Therefore, the new in-situ Al{sub 2}O{sub 3} pressure gauge is expected to enable new and expanded opportunities for offline laboratory studies of solid and liquid materials under high pressure and high temperature in multi-anvil apparatus.« less
Buoyancy-Driven, Rapid Exhumation of Ultrahigh-Pressure Metamorphosed Continental Crust
NASA Astrophysics Data System (ADS)
Ernst, W. G.; Maruyama, S.; Wallis, S.
1997-09-01
Preservation of ultrahigh-pressure (UHP) minerals formed at depths of 90-125 km require unusual conditions. Our subduction model involves underflow of a salient (250 ± 150 km wide, 90-125 km long) of continental crust embedded in cold, largely oceanic crust-capped lithosphere; loss of leading portions of the high-density oceanic lithosphere by slab break-off, as increasing volumes of microcontinental material enter the subduction zone; buoyancy-driven return toward midcrustal levels of a thin (2-15 km thick), low-density slice; finally, uplift, backfolding, normal faulting, and exposure of the UHP terrane. Sustained over ≈ 20 million years, rapid (≈ 5 mm/year) exhumation of the thin-aspect ratio UHP sialic sheet caught between cooler hanging-wall plate and refrigerating, downgoing lithosphere allows withdrawal of heat along both its upper and lower surfaces. The intracratonal position of most UHP complexes reflects consumption of an intervening ocean basin and introduction of a sialic promontory into the subduction zone. UHP metamorphic terranes consist chiefly of transformed, yet relatively low-density continental crust compared with displaced mantle material--otherwise such complexes could not return to shallow depths. Relatively rare metabasaltic, metagabbroic, and metacherty lithologies retain traces of phases characteristic of UHP conditions because they are massive, virtually impervious to fluids, and nearly anhydrous. In contrast, H2O-rich quartzofeldspathic, gneissose/schistose, more permeable metasedimentary and metagranitic units have backreacted thoroughly, so coesite and other UHP silicates are exceedingly rare. Because of the initial presence of biogenic carbon, and its especially sluggish transformation rate, UHP paragneisses contain the most abundantly preserved crustal diamonds.
NASA Astrophysics Data System (ADS)
Massonne, Hans-Joachim
2009-10-01
Phase relations of three common upper crustal rocks, quartz diorite, granite and evolved granite, with different water contents were studied by calculating P- T pseudosections with the computer program PERPLE_X for the range 0.5 to 4.5 GPa and 500 to 1250 °C. Of particular interest were the generation of fluids and the consumption of H 2O along various P- T paths typical for high-pressure and ultrahigh-pressure (UHP) metamorphism to better understand crustal rocks involved in deep-seated continent-continent collisional environments. The phase relations in all studied rock compositions are similar. Typically, jadeite/omphacite + phengite (Si apfu between 3.3 and 3.5) + garnet + coesite ± kyanite occur at UHP. At T < 700 °C, K-feldspar and lawsonite can also be present at "dry" and "wet" conditions, respectively. The exhumation of a lawsonite-absent UHP assemblage leads either to phengite-dehydration melting accompanied by garnet growth or, at slight cooling, to no dehydration whereas dehydration is typical for exhumation from depths corresponding to 1.5 GPa. These findings are applied to the UHP Sulu terrane in eastern China. The majority of gneisses of this terrane typically do not show garnet. It is assumed that these rocks are of low-pressure nature and would, thus, probably belong to the upper plate during Triassic continent-continent collision. The reported UHP gneisses occur locally, are associated with eclogites, experienced fluid infiltration at UHP, and were exhumed accompanied by slight cooling as no phengite-dehydration melting took place. These characteristics could point to metamorphism in a subduction channel.
Refinement of pressure calibration for multi-anvil press experiments
NASA Astrophysics Data System (ADS)
Ono, S.
2016-12-01
Accurate characterization of the pressure and temperature environment in high-pressure apparatuses is of essential importance when we apply laboratory data to the study of the Earth's interior. Recently, the synchrotron X-ray source can be used for the high-pressure experiments, and the in situ pressure calibration has been a common technique. However, this technique cannot be used in the laboratory-based experiments. Even now, the conventional pressure calibration is of great interest to understand the Earth's interior. Several high-pressure phase transitions used as the pressure calibrants in the laboratory-based multi-anvil experiments have been investigated. Precise determinations of phase boundaries of CaGeO3 [1], Fe2SiO4 [2], SiO2, and Zr [3] were performed by the multi-anvil press or the diamond anvil cell apparatuses combined with the synchrotron X-ray diffraction technique. The transition pressures in CaGeO3 (garnet-perovskite), Fe2SiO4 (alfa-gamma), and SiO2 (coesite-stishovite) were in general agreement with those reported by previous studies. However, significant discrepancies for the slopes, dP/dT, of these transitions between our and previous studies were confirmed. In the case of Zr study [3], our experimental results elucidate the inconsistency in the transition pressure between omega and beta phase in Zr observed in previous studies. [1] Ono et al. (2011) Phys. Chem. Minerals, 38, 735-740.[2] Ono et al. (2013) Phys. Chem. Minerals, 40, 811-816.[3] Ono & Kikegawa (2015) J. Solid State Chem., 225, 110-113.
NASA Technical Reports Server (NTRS)
Bose, Kunal; Ganguly, J.
1992-01-01
As part of our continued program of study on the volatile bearing phases and volatile resource potential of carbonaceous chondrite, results of our experimental studies on the dehydration kinetics of talc as a function of temperature and grain size (50 to 0.5 microns), equilibrium dehydration boundary of talc to 40 kbars, calorimetric study of enthalpy of formation of both natural and synthetic talc as a function of grain size, and preliminary results on the dehydration kinetics of epsomite are reported. In addition, theoretical calculations on the gas release pattern of Murchison meteorite, which is a C2(CM) carbonaceous chondrite, were performed. The kinetic study of talc leads to a dehydration rate constant for 40-50 microns size fraction of k = (3.23 x 10(exp 4))exp(-Q/RT)/min with the activation energy Q = 376 (plus or minus 20) kJ/mole. The dehydration rate was found to increase somewhat with decreasing grain size. The enthalpy of formation of talc from elements was measured to be -5896(10) kJ/mol. There was no measurable effect of grain size on the enthalpy beyond the limits of precision of the calorimetric studies. Also the calorimetric enthalpy of both synthetic and natural talc was found to be essentially the same, within the precision of measurements, although the natural talc had a slightly larger field of stability in our phase equilibrium studies. The high pressure experimental data the dehydration equilibrium of talc (talc = enstatite + coesite + H2O) is in strong disagreement with that calculated from the available thermochemical data, which were constrained to fit the low pressure experimental results. The calculated gas release pattern of Murchison meteorite were in reasonable agreement with that determined by stepwise heating in a gas chromatograph.
NASA Astrophysics Data System (ADS)
Tajčmanová, Lucie
2014-05-01
Metamorphic petrologists and structural geologists, using direct measurements, bring the only direct observational constrains for validating geodynamic models. Therefore, petrological and structural geological observations are essential for the quality and reproducibility of geodynamic reconstructions and models. One of the important assumptions for geodynamic reconstructions arises from the pressure and temperature estimates in the petrology analysis. Pressure is commonly converted to depth through the equation for lithostatic pressure and so the original position of the rock sample within the Earth's interior can be constrained. The current assumption that the studied sample corresponds to uniform pressure may not be correct, and if so, it has serious implications. Increasing evidence from analytical data shows that pressure is not constant even on a grain scale, posing new challenges because, if ignored, it leads to an incorrect use of petrology data in constraining geodynamic models. Well known examples of the preservation of coesite and diamond in a host mineral like garnet show that high pressure inclusions are preserved during decompression. Tajčmanová et al. (2014) has shown that grain-scale pressure variations can develop and that these pressure variations allow compositional zoning in minerals preserved over geological time scales. A new unconventional barometric method based on equilibrium under pressure variations has been developed . Such pressure variations are also connected with differences in fluid pressure in open systems and can be thus observed at all scales. Tajčmanová L., Podladchikov Y., Powell R., Moulas E., Vrijmoed J. and Connolly J. (2014). Grain scale pressure variations and chemical equilibrium in high-grade metamorphic rocks.Journal of Metamorphic Geology, doi:10.1111/jmg.12066 This work was supported by ERC starting grant 335577 to Lucie Tajcmanova
Russian-US Partnership to Study the 23-km-diameter El'gygtgyn Impact Crater, Northeast Russia
NASA Technical Reports Server (NTRS)
Sharpton, Virgil L.; Minyuk, Pavel S.; Brigham-Grette, Julie; Glushkova, Olga; Layer, Paul; Raikevich, Mikhail; Stone, David; Smirnov, Valdimir
2002-01-01
El'gygytgyn crater, located within Eastern Siberia, is a Pliocene-aged (3.6 Ma), well-preserved impact crater with a rim diameter of roughly 23 km. The target rocks are a coherent assemblage of crystalline rocks ranging from andesite to basalt. At the time of impact the region was forested and the Arctic Ocean was nearly ice-free. A 15-km lake fills the center of the feature and water depths are approximately 175 m. Evidence of shock metamorphism, -- including coesite, fused mineral glasses, and planar deformation features in quartz -- has been reported. This feature is one of the youngest and best preserved complex craters on Earth. Because of its remote Arctic setting, however, El gygytgyn crater remains poorly investigated. The objectives of this three-year project are to establish and maintain a research partnership between scientists from Russia and the United States interested in the El gygytgyn crater. The principal institutions in the U.S. will be the Geophysical Institute, University of Alaska Fairbanks and the University of Massachusetts Amherst. The principal institution in Russia will be the North East Interdisciplinary Scientific Research Institute (NEISRI), which is the Far-East Branch of the Russian Academy of Science. Three science tasks are identified for the exchange program: (1) Evaluate impactite samples collected during previous field excursions for evidence of and level of shock deformation. (2) Build a high-resolution digital elevation model for the crater and its surroundings using interferometric synthetic aperture radar techniques on JERS-1, ERS-1, ERS-2, and/or RadarSat range-doppler data. (3) Gather all existing surface data available from Russian and U.S. institutions (DEM, remote sensing image data, field-based lithological and sample maps, and existing geophysical data) and assemble into a Geographic Information Systems database.
NASA Astrophysics Data System (ADS)
Liu, F.; Gerdes, A.; Xue, H.; Liang, F.
2006-12-01
Eclogite as lenses in impure marbles from Dabie-Sulu UHP terrane, represent parts of deeply subducted meta- sedimentary rocks. To constrain the age of metamorphism during subduction and exhumation, zircons from 2 eclogite samples in Dabie-Sulu impure marbles have been investigated. Beside Inherited (detrital) grains, 3 different metamorphic zircon domains have been identified based on distribution of mineral inclusion, trace elements and cathodoluminescence (CL) imaging: 1. Dark-luminescent rounded cores with quartz eclogite- facies mineral inclusions suggest formation at high-pressure (HP) metamorphic conditions. 2. White- luminescent zircon, either surrounding domain 1 or as rounded to spindly cores with index coesite eclogite- facies mineral inclusions indicates formation at UHP conditions. 3. Grey-luminescent rims around domain 2 with low-pressure mineral inclusions suggest formation during late regional amphibolite-facies retrogression. The three distinct zircon domains were dated by SHRIMP and yielded three discrete and meaningful age groups: 245±4 Ma for prograde HP metamorphism, 235±3 Ma for UHP metamorphism and 215±6 Ma for late amphibolite-facies retrogression from Dabie-Sulu eclogite. This data suggests that subduction and exhumation took place in about 10-11 Myr and 19-20 Myr, respectively. Continental materials was subducted from surface to the deep mantle depth at rates of 10 km/Myr, and subsequently exhumed from the mantle to the base of the crust at rates of 7 km/Myr. Ultrafast exhumation of the Dabie-Sulu UHP terrane from depth of 160 to 30 km was probably driven by buoyancy forces after UHP slab break-off at deep mantle depths.
The first allanite-bearing eclogite xenolith in kimberlite
NASA Astrophysics Data System (ADS)
Trojman-Nichols, S.; Heaman, L.
2015-12-01
Here we report the first allanite-bearing mantle eclogite xenolith, entrained in the 173 Ma Jericho kimberlite pipe, located in the Slave craton, northwestern Canada. This eclogite is unique among the other Jericho eclogites by an extreme LREE enrichment in all phases, and garnet alteration rims that are more calcic than the garnet cores. Allanite is an abundant accessory phase, present as dull orange, subhedral crystals. Other minerals in the paragenesis are garnet, clinopyroxene, apatite and sulfides; two compositionally and texturally distinct generations of phlogopite constitute a secondary paragenesis where allanite is no longer stable. Allanite in this sample is La-, Ce- and Th- rich, with concentrations at the weight % level, while Y is only present at the relatively low concentration of ~100 ppm. Electron backscatter imaging reveals complex zonation within the allanite crystals that is off-centre, non-symmetric, and patchy. It is often asserted that eclogite xenoliths represent subducted oceanic lithosphere, despite significant differences in the composition and mineralogy between mantle-derived eclogite xenoliths and eclogite massif material. Both types of eclogite occurrences can contain quartz/coesite; massif eclogites often have small, sparse allanite inclusions, but allanite has never been reported in eclogite xenoliths in kimberlite. Allanite in massif eclogite is thought to form during subduction by the break-down of lawsonite and the incorporation of LREE into zoisite. Lawsonite breaks down into grossular and H20 at high pressures, which may explain the anomalous high-Ca rims measured in some garnets in this sample. This allanite-bearing eclogite may provide an unprecedented window for exploring a crucial stage of eclogite metamorphism and fluid mobilization in subduction zones. In addition, the U-Pb systematics currently under investigation may constrain the age of eclogitization.
NASA Astrophysics Data System (ADS)
Grevel, Klaus-Dieter; Schoenitz, Mirko; Skrok, Volker; Navrotsky, Alexandra; Schreyer, Werner
2001-08-01
The enthalpy of drop-solution in molten 2PbO.B2O3 of synthetic and natural lawsonite, CaAl2(Si2O7)(OH)2.H2O, was measured by high-temperature oxide melt calorimetry. The enthalpy of formation determined for the synthetic material is ΔfHOxides=-168.7+/-3.4 kJ mol-1, or ΔfH0298=-4,872.5+/-4.0 kJ mol-1. These values are in reasonable agreement with previously published data, although previous calorimetric work yielded slightly more exothermic data and optimisation methods resulted in slightly less exothermic values. The equilibrium conditions for the dehydration of lawsonite to zoisite, kyanite and quartz/coesite at pressures and temperatures up to 5 GPa and 850 °C were determined by piston cylinder experiments. These results, other recent phase equilibrium data, and new calorimetric and thermophysical data for lawsonite and zoisite, Ca2Al3(SiO4)(Si2O7)O(OH), were used to constrain a mathematical programming analysis of the thermodynamic data for these two minerals in the chemical system CaO-Al2O3-SiO2-H2O (CASH). The following data for lawsonite and zoisite were obtained: ΔfH0298 (lawsonite)=-4,865.68 kJ mol-1 , S0298 (lawsonite)=229.27 J K-1 mol-1 , ΔfH0298 (zoisite)=-6,888.99 kJ mol-1 , S0298 (zoisite)=297.71 J K-1 mol-1 . Additionally, a recalculation of the bulk modulus of lawsonite yielded K=120.7 GPa, which is in good agreement with recent experimental work.
Partial melting of UHP calc-gneiss from the Dabie Mountains
NASA Astrophysics Data System (ADS)
Liu, Penglei; Wu, Yao; Liu, Qiang; Zhang, Junfeng; Zhang, Li; Jin, Zhenmin
2014-04-01
Exhumation melting has been proposed for the ultra-high pressure (UHP) metamorphic rocks in the Dabie Mountains based on melting experiments. We document here the first petrological and mineralogical evidence demonstrating that the UHP calc-gneisses from the Ganjialing area in the Dabie Mountains experienced partial melting during early exhumation. The assemblage of garnet, phengite (Si = 3.65 pfu), coesite, rutile and carbonate preserved in the calc-gneisses indicates a peak metamorphic condition of 692-757 °C and 4.0-4.8 GPa. Partial melting is indicated by several lines of evidence: the melting textures of phengite, the feldspar-dominated films, bands, branches, blebs and veins, the euhedral K-feldspars, the intergrowth film of plagioclase and K-feldspar, the plagioclase + biotite intergrowth after garnet and the epidote poikiloblasts. Polyphase inclusions in garnet are characterized with wedge-like offshoots and serrate outlines whereas those in epidote display negative crystal shapes, which can be best interpreted by entrapment of former melts. We propose a wet melting reaction of Phn + Q ± Na-Cpx + H2O = Bt + Pl + Grt + felsic melts, which likely took place at ca.650-800 °C and ca.1.0-2.0 GPa, to interpret the melting event in the calc-gneisses. Chemical exchanges between garnet and melts produced new garnet domains with higher almandine, spessartine, MREE, HREE and Y but lower grossular, pyrope, P, Sc, Ti, V and Zr contents. Zr-in-rutile thermometer reveals a low temperature of 620-643 °C at 5 GPa, indicating a later reset for Zr in rutile. Healed fractures are suggested to be responsible for the formation of some polyphase inclusions in garnet.
Age and duration of eclogite-facies metamorphism, North Qaidam HP/UHP terrane, Western China
Mattinson, C.G.; Wooden, J.L.; Liou, J.G.; Bird, D.K.; Wu, C.L.
2006-01-01
Amphibolite-facies para-and orthogneisses near Dulan, at the southeast end of the North Qaidam terrane, enclose minor eclogite and peridotite which record ultra-high pressure (UHP) metamorphism associated with the Early Paleozoic continental collision of the Qilian and Qaidam microplates. Field relations and coesite inclusions in zircons from paragneiss suggest that felsic, mafic, and ultramafic rocks all experienced UHP metamorphism and a common amphibolite-facies retrogression. SHRIMP-RG U-Pb and REE analyses of zircons from four eclogites yield weighted mean ages of 449 to 422 Ma, and REE patterns (flat HREE, no Eu anomaly) and inclusions of garnet, omphacite, and rutile indicate these ages record eclogite-facies metamorphism. The coherent field relations of these samples, and the similar range of individual ages in each sample suggests that the ???25 m.y. age range reflects the duration of eclogite-facies conditions in the studied samples. Analyses from zircon cores in one sample yield scattered 433 to 474 Ma ages, reflecting partial overlap on rims, and constrain the minimum age of eclogite protolith crystallization. Inclusions of Th + REE-rich epidote, and zircon REE patterns are consistent with prograde metamorphic growth. In the Lu??liang Shan, approximately 350 km northwest in the North Qaidam terrane, ages interpreted to record eclogite-facies metamorphism of eclogite and garnet peridotite are as old as 495 Ma and as young as 414 Ma, which suggests that processes responsible for extended high-pressure residence are not restricted to the Dulan region. Evidence of prolonged eclogite-facies metamorphism in HP/UHP localities in the Northeast Greenland eclogite province, the Western Gneiss Region of Norway, and the western Alps suggests that long eclogite-facies residence may be globally significant in continental subduction/collision zones.
NASA Astrophysics Data System (ADS)
Solarino, Stefano; Malusà, Marco G.; Eva, Elena; Guillot, Stéphane; Paul, Anne; Schwartz, Stéphane; Zhao, Liang; Aubert, Coralie; Dumont, Thierry; Pondrelli, Silvia; Salimbeni, Simone; Wang, Qingchen; Xu, Xiaobing; Zheng, Tianyu; Zhu, Rixiang
2018-01-01
In continental subduction zones, the behaviour of the mantle wedge during exhumation of (ultra)high-pressure [(U)HP] rocks provides a key to distinguish among competing exhumation mechanisms. However, in spite of the relevant implications for understanding orogenic evolution, a high-resolution image of the mantle wedge beneath the Western Alps is still lacking. In order to fill this gap, we perform a detailed analysis of the velocity structure of the Alpine belt beneath the Dora-Maira (U)HP dome, based on local earthquake tomography independently validated by receiver function analysis. Our results point to a composite structure of the mantle wedge above the subducted European lithosphere. We found that the Dora-Maira (U)HP dome lays directly above partly serpentinized peridotites (Vp 7.5 km/s; Vp/Vs = 1.70-1.72), documented from 10 km depth down to the top of the eclogitized lower crust of the European plate. These serpentinized peridotites, possibly formed by fluid release from the subducting European slab to the Alpine mantle wedge, are juxtaposed against dry mantle peridotites of the Adriatic upper plate along an active fault rooted in the lithospheric mantle. We propose that serpentinized mantle-wedge peridotites were exhumed at shallow crustal levels during late Eocene transtensional tectonics, also triggering the rapid exhumation of (U)HP rocks, and were subsequently indented under the Alpine metamorphic wedge in the early Oligocene. Our findings suggest that mantle-wedge exhumation may represent a major feature of the deep structure of exhumed continental subduction zones. The deep orogenic levels here imaged by seismic tomography may be exposed today in older (U)HP belts, where mantle-wedge serpentinites are commonly associated with coesite-bearing continental metamorphic rocks.
Cavosie, Aaron; Timms, Nicholas E.; Erickson, Timmons M.; Hagerty, Justin J.; Hörz, Friedrich
2016-01-01
Granular zircon in impact environments has long been recognized but remains poorly understood due to lack of experimental data to identify mechanisms involved in its genesis. Meteor Crater in Arizona (United States) contains abundant evidence of shock metamorphism, including shocked quartz, the high pressure polymorphs coesite and stishovite, diaplectic SiO2 glass, and lechatelierite (fused SiO2). Here we report the presence of granular zircon, a new shocked mineral discovery at Meteor Crater, that preserve critical orientation evidence of specific transformations that occurred during its formation at extreme impact conditions. The zircon grains occur as aggregates of sub-µm neoblasts in highly shocked Coconino Formation Sandstone (CFS) comprised of lechatelierite. Electron backscatter diffraction shows that each grain consists of multiple domains, some with boundaries disoriented by 65°, a known {112} shock-twin orientation. Other domains have crystallographic c-axes in alignment with {110} of neighboring domains, consistent with the former presence of the high pressure ZrSiO4 polymorph reidite. Additionally, nearly all zircon preserve ZrO2 + SiO2, providing evidence of partial dissociation. The genesis of CFS granular zircon started with detrital zircon that experienced shock-twinning and reidite formation from 20 to 30 GPa, ultimately yielding a phase that retained crystallographic memory; this phase subsequently recrystallized to systematically oriented zircon neoblasts, and in some areas partially dissociated to ZrO2. The lechatelierite matrix, experimentally constrained to form at >2000 °C, provided an ultra high-temperature environment for zircon dissociation (~1670 °C) and neoblast formation. The capacity of granular zircon to preserve a cumulative P-T record has not been recognized previously, and provides a new method for retrieving histories of impact-related mineral transformations in the crust at conditions far beyond which most rocks melt.
Dynamic compression of minerals in the magnesium oxide-iron oxide-silicon dioxide system
NASA Astrophysics Data System (ADS)
Akins, Joseph A.
The first shock wave experiments performed on silicate materials were reported for quartz in 1962. The intervening forty years have allowed for extensive investigation of SiO2 by dynamic, static and theoretical means. Previous studies have concluded that quartz transforms completely to stishovite at ˜40 GPa and melts at ˜115 GPa along its Hugoniot. Recent discoveries that SiO2 transforms to phases slightly more dense than stishovite have led to a reexamination of the dynamic compression of SiO2 in this thesis. Based on comparing calculated Hugoniots to data for multiple initial SiO2 phases, it is proposed that, in addition to the stishovite and melt transitions, quartz is completely transformed to the CaCl2 structure at ˜70 GPa. Coesite shows evidence of complete transformation to stishovite at ˜50 GPa, and to the CaCl 2 structure at ˜65 GPa. Due to the higher temperature achieved in the quartz samples the slope of the stishovite-CaCl2 phase boundary is constrained to be ˜180 K/GPa. From a similar analysis of Hugoniot data collected for high quality MgSiO 3 natural crystal and synthetic glass in this study, and existing data, it is concluded that along the crystal Hugoniot akimotoite is attained at ˜70 GPa, perovskite structure at ˜110 GPa and melt at ˜170 GPa. It is found that the melt is 2--3% denser than the solid at pressures greater than 100 GPa, after correcting for thermal differences in the two regimes. An important implication is a negative Clapeyron slope, leading to a decreasing melting temperature with increasing pressure, above ˜100 GPa. These observations increase the possibility of the existence of a significant amount of partial melt in the lowermost mantle, e.g., the ultra low velocity zone.
Horton, J. Wright; Kunk, Michael J.; Belkin, Harvey E.; Aleinikoff, John N.; Jackson, John C.; Chou, I.-Ming
2009-01-01
The 1766-m-deep Eyreville B core from the late Eocene Chesapeake Bay impact structure includes, in ascending order, a lower basement-derived section of schist and pegmatitic granite with impact breccia dikes, polymict impact breccias, and cataclas tic gneiss blocks overlain by suevites and clast-rich impact melt rocks, sand with an amphibolite block and lithic boulders, and a 275-m-thick granite slab overlain by crater-fill sediments and postimpact strata. Graphite-rich cataclasite marks a detachment fault atop the lower basement-derived section. Overlying impactites consist mainly of basement-derived clasts and impact melt particles, and coastal-plain sediment clasts are underrepresented. Shocked quartz is common, and coesite and reidite are confirmed by Raman spectra. Silicate glasses have textures indicating immiscible melts at quench, and they are partly altered to smectite. Chrome spinel, baddeleyite, and corundum in silicate glass indicate high-temperature crystallization under silica undersaturation. Clast-rich impact melt rocks contain α-cristobalite and monoclinic tridymite. The impactites record an upward transition from slumped ground surge to melt-rich fallback from the ejecta plume. Basement-derived rocks include amphibolite-facies schists, greenschist(?)-facies quartz-feldspar gneiss blocks and subgreenschist-facies shale and siltstone clasts in polymict impact breccias, the amphibolite block, and the granite slab. The granite slab, underlying sand, and amphibolite block represent rock avalanches from inward collapse of unshocked bedrock around the transient crater rim. Gneissic and massive granites in the slab yield U-Pb sensitive high-resolution ion microprobe (SHRIMP) zircon dates of 615 ± 7 Ma and 254 ± 3 Ma, respectively. Postimpact heating was <~350 °C in the lower basement-derived section based on undisturbed 40Ar/39Ar plateau ages of muscovite and <~150 °C in sand above the suevite based on 40Ar/39Ar age spectra of detrital microcline.
NASA Astrophysics Data System (ADS)
Zhang, Yanfei; Wu, Yao; Wang, Chao; Zhu, Lüyun; Jin, Zhenmin
2016-08-01
The subducted continental crust material will be gravitationally trapped in the deep mantle after having been transported to depths of greater than ∼250-300 km (the "depth of no return"). However, little is known about the status of this trapped continental material as well as its contribution to the mantle heterogeneity after achieving thermal equilibrium with the surrounding mantle. Here, we conduct an experimental study over pressure and temperature ranges of 9-16 GPa and 1300-1800 °C to constrain the fate of these trapped upper continental crust (UCC). The experimental results show that partial melting will occur in the subducted UCC along normal mantle geotherm to produce K-rich melt. The residual phases composed of coesite/stishovite + clinopyroxene + kyanite in the upper mantle, and stishovite + clinopyroxene + K-hollandite + garnet + CAS-phase in the mantle transition zone (MTZ), respectively. The residual phases achieve densities greater than the surrounding mantle, which provides a driving force for descent across the 410-km seismic discontinuity into the MTZ. However, this density relationship is reversed at the base of the MTZ, leaving the descended residues to be accumulated above the 660-km seismic discontinuity and may contribute to the "second continent". The melt is ∼0.6-0.7 g/cm3 less dense than the surrounding mantle, which provides a buoyancy force for ascent of melt to shallow depths. The ascending melt, which preserves a significant portion of the bulk-rock rare earth elements (REEs), large ion lithophile elements (LILEs), and high-filed strength elements (HFSEs), may react with the surrounding mantle. Re-melting of the metasomatized mantle may contribute to the origin of the "enriched mantle sources" (EM-sources). Therefore, the deep subducted continental crust may create geochemical/geophysical heterogeneity in Earth's interior through subduction, stagnation, partial melting and melt segregation.
Microdiamonds from the European Variscan Orogenic Belt
NASA Astrophysics Data System (ADS)
Kotkova, J.; Jakubova, P.; Whitehouse, M.; Fedortchouk, Y.
2014-12-01
Diamond, along with coesite, has been discovered recently in the continental crustal rocks of the European Variscan orogenic belt, namely the Bohemian Massif (BM). In addition to the garnet-phengite gneiss in Germany, western BM, microdiamond occurs in major rock forming minerals - garnet, kyanite - and in zircon in ultrahigh-pressure rocks overprinted under high-pressure granulite facies conditions (c. 16-20 kbar, c. 1000°C) in the northern and eastern BM. Well-preserved 10-30 μm-sized microdiamonds from northern BM exhibit diverse morphologies (SEM data) depending upon the host rock type. Octahedral diamond occurs in felsic garnet-kyanite-feldspar-quartz rock (metasediment), whereas intermediate garnet-clinopyroxene-feldspar-quartz rock contains a cubo-octahedral variety. Diamond morphology can be thus controlled by solid impurities available in the medium of crystallization (K- vs. Ca-bearing fluids or melts), as shown by experiments. Pointed-bottom negatively oriented trigonal etch pits on the octahedral diamond faces developed due to diamond resorption at CO2-dominated environment (less than 50 wt % of H2O, experimental data), possibly by action of a residual fluid. SIMS determined δ13C values range from -22 to -21 ‰ for the felsic rock and from - 26 to - 33 for the intermediate one, corresponding to the typical range of organic carbon δ13C and inconsistent with a significant mantle carbon (δ13C ~ - 5 ‰) input. Diamond-bearing domains in zircon, also analysed by SIMS, yielded a Variscan U-Pb age of c. 340 Ma. The present stage of knowledge allows us to conclude that (i) metamorphic diamonds in the BM occur in lithologies of metasedimentary character, and their carbon source was organic; (ii) crustal-derived CO2-rich fluids with impurities played an important role in diamond formation and dissolution; (iii) diamonds formed during the Variscan orogenic cycle and (iv) diamonds are best preserved in the external domain of the Variscan orogenic belt.
Zhou, Yun; Ning, Xun-an; Liao, Xikai; Lin, Meiqing; Liu, Jingyong; Wang, Jianghui
2013-09-01
The environmental risk of exposure to six heavy metals (Cu, Pb, Zn, Cr, Ni, and Cd) found in fly ashes from waste filter bags obtained from a steel plant was estimated based on the mineralogical compositions, total concentrations and speciation of the metals in the fly ashes. The results indicated that the fly ashes mainly consisted of hematite, magnetite, cyanite, spinel, coesite and amorphous materials. The concentrations of Zn and Pb were much higher than that of other materials. After Zn and Pb, Ni was present in the highest concentration, followed by Cu, Cr and Cd. Each heavy metal was distributed differently in fly ashes. The levels of Zn, Cd and Pb in the active fraction were very high, and ranged from 64.83 to 81.96%, 34.48 to 82.4% and 6.92 to 79.65% respectively, while Cu, Cr and Ni were mainly present in the residual fraction. The risk assessment code (RAC) values of fly ashes showed that the Zn and Cd present in the H3 sample presented a very high risk, with RAC values greater than 50%. The Cu present in the H3 sample, Cd in the H2 sample and Zn in the H4 and H5 samples presented a high risk. The Pb present in the H2 sample, Cd in the H4 sample, Ni in the H1 and H5 samples, and Zn in the H1 sample presented a medium risk. A low risk was presented by the Cu present in the H1, H2, H4 and H5 samples, the Pb in the H1, H3 and H5 samples, the Cd in the H1 and H5 samples, and the Ni in the H2 sample. No risk was presented by Cr in any sample. Copyright © 2013 Elsevier Inc. All rights reserved.
NASA Astrophysics Data System (ADS)
Peterman, E. M.; Hacker, B. R.; Kylander-Clark, A. R.
2005-12-01
Evidence for (ultra)high-pressure --(U)HP-- metamorphism in modern orogenic belts and the preservation of exhumed (U)HP terranes around the world suggest that subduction and exhumation of continental crust plays an important role in Phanerozoic plate tectonics. The Western Gneiss region (WGR) of Norway, a major (U)HP province extending over 60,000 km2, provides an excellent opportunity to study how subduction to depths >100 km affects continental crust. By studying a ~60 km wide transect bounded to the north by Vartdalsfjorden and Rovdefjorden and the south by the Möre og Romsdal county boundary, we are able to examine mineralogical changes that occurred during subduction and exhumation within a rock composed predominantly of orthogneiss and variably transformed mafic bodies, which indicate the depths to which these rocks were subducted. Previous studies (e.g. Hacker et al., 2005) have suggested that Caledonian deformation in WGR host gneisses is primarily limited to brittle-ductile fabrics characterized by greenschist to lower-amphibolite facies metamorphism; the majority of the deformation in the rocks, including the pervasive foliation and foliation-parallel isoclinal folds, occurred between 1200 and 900 Ma. On the northern half of our study area, however, locally occurring neoblastic garnet crosscuts the foliation in the gneiss. The boundary of this garnet zone coincides with the local HP-UHP boundary, as determined by the presence of coesite in eclogite. Because garnet can retain information about changes in pressure and temperature, as well as the availability of water within the crust to catalyze chemical reactions, our findings suggest that 1) portions of the orthogneiss did transform at high pressures, 2) the presence of garnet within the orthogneiss may indicate conditions that approximate UHP and can therefore be useful in defining the boundaries between UHP and HP conditions, and 3) the growth of garnet during (U)HP metamorphism may be controlled by hydration of the crust, thus explaining the partial transformation to (U)HP mineral assemblages throughout the WGR.
Raman spectroscopy of detrital garnet from the (U)HP terrane of eastern Papua New Guinea
NASA Astrophysics Data System (ADS)
Andò, Sergio; Baldwin, Suzanne L.; Fitzgerald, Paul G.; Malusà, Marco G.; Aliatis, Irene; Vezzoli, Giovanni; Garzanti, Eduardo
2013-04-01
Garnet is one of the most widespread heavy minerals in sediments derived from orogenic systems. Its chemical composition varies systematically with temperature and pressure conditions, and thus provides information on the metamorphic evolution of source areas that is crucial in tectonic and geodynamic reconstructions. Garnet is easily identified in mineral grain mounts and is relatively stable during burial diagenesis. Raman spectroscopy allows rapid determination of garnet compositions in grain mounts or thin sections of sand and sandstone samples, and can be used to assess their density and chemical composition quite accurately ("MIRAGEM" method of Bersani et al., 2009; Andò et al., 2009). In the D'Entrecastreaux Islands of southeastern Papua New Guinea, the world's youngest (U)HP rocks are exposed. There, mafic rocks and their felsic host gneisses were metamorphosed under eclogite facies conditions from late Miocene to Pliocene, before being exhumed from depths of ~90 km (Baldwin et al., 2004, 2008). The eclogite preserves a peak assemblage of garnet, omphacite, rutile, phengite and Si02 (Hill and Baldwin, 1993). A coesite-eclogite has been found in one small island outcrop. In order to sample garnet populations representative of a larger geographical area, we sampled and studied a heavy-mineral-dominated placer sand (HMC 80) from a beach from SE Goodenough Island. Garnet grains in beach sand are associated with blue-green to subordinately green-brown amphibole and minor epidote, omphacitic clinopyroxene, titanite, apatite and rutile. The subordinate low-density fraction is feldspatho-quartzose with high-rank metamorphic rock fragments and biotite (Q62 F35 Lm2; MI 360). Detrital garnets are mostly classified as almandine with relatively high Mg and Ca and lacking Mn, typical of the eclogite facies (Win et al., 2007; type Ci garnets of Mange and Morton 2007; Andò et al., 2013). In well-described stratigraphic sequences within syn-and post-tectonic basins adjacent to orogenic systems, Raman-assisted heavy-mineral studies allow us to detect the first arrival of eclogitic garnet, and thus to assess the minimum age of exhumation and final unroofing of high-pressure rocks (Malusà et al., 2011; Malusà and Garzanti, 2012). However, in the (U)HP terrane of southeastern Papua New Guinea, sediments derived from the actively exhuming D'Entrecasteaux Island core complexes are still being deposited offshore, are rarely preserved sub-aerially, and as such stratigraphic constraints are limited. Raman analysis of detrital garnets from placer sand thus provides invaluable constraints to compare with mineral assemblages preserved in exhumed eclogites. REFERENCES Andò S., Bersani D., Vignola P., Garzanti E. 2009. Raman spectroscopy as an effective tool for high-resolution heavy-mineral analysis: Examples from major Himalayan and Alpine fluvio-deltaic systems. Spectrochim. Acta A73:450-455. Andò S., Morton A., Garzanti E. 2013. Metamorphic grade of source rocks revealed by chemical fingerprints of detrital amphibole and garnet. Geol. Soc. London Spec. Publ. Sediment Provenance Studies in Hydrocarbon Exploration & Production. Baldwin S.L., Monteleone B., Webb L.E., Fitzgerald P.G., Grove M., Hill E.J. 2004. Pliocene eclogite exhumation at plate tectonic rates in eastern Papua New Guinea. Nature 431:263-267. Baldwin S.L., Webb L.E., Monteleone B.D. 2008. Late Miocene coesite-eclogite exhumed in the Woodlark Rift. Geology 36:735-738 Bersani D., Andò S., Vignola P., Moltifiori G., Marino I.G., Lottici P.P., Diella V., 2009. Micro-Raman spectroscopy as a routine tool for garnet analysis. Spectrochim. Acta A73:484-491. Hill E.J., Baldwin S.L. 1993. Exhumation of high-pressure metamorphic rocks during crustal extension in the D'Entrecasteaux region, Papua New Guinea. J. Metam. Geol. 11:261-277. Malusà M.G., Faccenna C., Garzanti E., Polino R. 2011. Divergence in subduction zones and exhumation of high-pressure rocks (Eocene Western Alps). Earth Pl. Sci. Lett. 310:21-32. Malusà M.G., Garzanti E. 2012. Actualistic snapshot of the early Oligocene Alps: the Alps-Apennines knot detangled. Terra Nova 24:1-6. Mange M.A., Morton A.C. 2007. Geochemistry of Heavy Minerals. In: Mange, M.A. & Wright, D.T. (Eds) Heavy Minerals in Use, Developments in Sedimentology 58:345-391. Win K.S., Takeuchi M., Tokiwa T. 2007. Changes in detrital garnet assemblages related to transpressive uplifting associated with strike-slip faulting: an example from the Cretaceous System in Kii Peninsula, southwest Japan. Sedim. Geol. 201:412-431.
NASA Astrophysics Data System (ADS)
Korolev, N. M.; Kopylova, M.; Bussweiler, Y.; Pearson, D. G.; Gurney, J.; Davidson, J.
2018-04-01
The mantle beneath the Cullinan kimberlite (formerly known as "Premier") is a unique occurrence of diamondiferous cratonic mantle where diamonds were generated contemporaneously and shortly following a mantle upwelling that led to the formation of a Large Igneous Province that produced the world's largest igneous intrusion - the 2056 Ma Bushveld Igneous Complex (BIC). We studied 332 diamond inclusions from 202 Cullinan diamonds to investigate mantle thermal effects imposed by the formation of the BIC. The overwhelming majority of diamonds come from three parageneses: (1) lithospheric eclogitic (69%), (2) lithospheric peridotitic (21%), and (3) sublithospheric mafic (9%). The lithospheric eclogitic paragenesis is represented by clinopyroxene, garnet, coesite and kyanite. Main minerals of the lithospheric peridotitic paragenesis are forsterite, enstatite, Cr-pyrope, Cr-augite and spinel; the sublithospheric mafic association includes majorite, CaSiO3 phases and omphacite. Diamond formation conditions were calculated using an Al-in-olivine thermometer, a garnet-clinopyroxene thermometer, as well as majorite and Raman barometers. The Cullinan diamonds may be unique on the global stage in recording a cold geotherm of 40 mW/m2 in cratonic lithosphere that was in contact with underlying convecting mantle at temperatures of 1450-1550 °C. The studied Cullinan diamonds contain a high proportion of inclusions equilibrated at temperatures exceeding the ambient 1327 °C adiabat, i.e. 54% of eclogitic diamonds and 41% of peridotitic diamonds. By contrast, ≤ 1% of peridotitic diamond inclusions globally yield equally high temperatures. We propose that the Cullinan diamond inclusions recorded transient, slow-dissipating thermal perturbations associated with the plume-related formation of the 2 Ga Bushveld igneous province. The presence of inclusions in diamond from the mantle transition zone at 300-650 km supports this view. Cullinan xenoliths indicative of the thermal state of the cratonic lithosphere at 1.2 Ga are equilibrated at the relatively low temperatures, not exceeding adiabatic. The ability of diamonds to record super-adiabatic temperatures may relate to their entrainment from the deeper, hotter parts of the upper mantle un-sampled by the kimberlite in the form of xenoliths or their equilibration in a younger lithosphere after a decay of the thermal disturbance.
Thermobaric structure of the Himalayan Metamorphic Belt in Kaghan Valley, Pakistan
NASA Astrophysics Data System (ADS)
Rehman, Hafiz Ur; Yamamoto, Hiroshi; Kaneko, Yoshiyuki; Kausar, Allah Bakhsh; Murata, Mamoru; Ozawa, Hiroaki
2007-02-01
The thermobaric structure of the Himalayan Metamorphic Belt (HMB) has been constructed along the Kaghan Valley transect, Pakistan. The HMB in this valley represents mainly the Lesser Himalayan Sequence (LHS) and Higher Himalayan Crystallines (HHC). Mineral parageneses of 474 samples, from an approximately, 80-km traverse from southwest to northeast, were examined. Microprobe analyses were carried out to quantify the mineral composition. To determine the pressure-temperature (P-T) conditions, 65 thin sections (7 pelites from LHS and 25 pelites, 9 mafic rocks/amphibolites and 19 eclogites from HHC) were selected. Based on field observations and mineral paragenesis, low-grade to high-grade metapelites, show Barrovian-type progressive metamorphic sequence, with chlorite, biotite, garnet and staurolite zones in LHS and staurolite, kyanite and sillimanite zones in HHC. By using well-calibrated geothermobarometers, P-T conditions for pelitic and mafic rocks are estimated. P-T estimates for pelitic rocks from the garnet zone indicate a condition of 534 ± 17 °C at 7.6 ± 1.2 kbar. P-T estimates for rocks from the staurolite and kyanite zones indicate average conditions of 526 ± 17 °C at 9.4 ± 1.2 kbar and 657 ± 54 °C at 10 ± 1.6 kbar, respectively. P-T conditions for mafic rocks (amphibolites) and eclogites from HHC are estimated as 645 ± 54 °C at 10.3 ± 2 kbar and 746 ± 59 °C at 15.5 ± 2.1 kbar, respectively. The coesite-bearing ultrahigh-pressure (UHP) eclogites record a peak P-T condition of 757-786 °C at 28.6 ± 0.4 kbar and retrograde P-T conditions of 825 ± 59 °C at 18.1 ± 1.7 kbar. These results suggest that HMB show a gradual increase in metamorphic grade from southwest to northeast. The P-T conditions from Pelitic and adjacent mafic rocks having identical peak conditions in the same metamorphic zone, while the structural middle in HHC reached the highest P-T condition upto the UHP grade.
SiO2 Solubility in Rutile at High Pressure and Temperature
NASA Astrophysics Data System (ADS)
Ren, Y.; Fei, Y.; Yang, J.; Bai, W. J.; Xu, Z. Q.
2005-12-01
Silicon-bearing rutile has been found in nature. The extent of SiO2 solubility in rutile and the nature of its origin are still not clear. At high pressure, SiO2 takes rutile structure with 6-coordinated Si. The high-pressure phase of SiO2 may enhance its solubility in rutile because possible isovalent exchange in octahedral site. In this study, we report new experimental results on SiO2 solubility in rutile up to 23 GPa and 2273 K. Starting materials are mixtures of powdered TiO2 and SiO2, with compositions of (Ti0.5Si0.5)O2, (Ti0.93Si0.07)O2, and (Ti0.75Si0.25)O2. The mixtures were loaded into either a platinum capsules (for a 10/5 assembly) or a rhenium capsules (for an 8/3 assembly). The experiments were carried out using multi-anvil high-pressure apparatus with rhenium resistance heater. Sample temperatures were measured with a type-C thermocouple. The quenched samples were recovered and prepared for electron microprobe analyses. TiO2-rich and SiO2-rich phases are produced in all the quenched samples. The analyses showed that the solubility of SiO2 in rutile increases with increasing pressure, from 1.5 wt% SiO2 at 10 GPa to 3.8 wt% SiO2 at 23 GPa for a given temperature of 2073 K. The solubility also increases with increasing temperature, from 0.5 wt% SiO2 at 1773 K to 4.5 wt% SiO2 at 2273 K for a given pressure of 18 GPa. On the other hand, the solubility of TiO2 in coesite or stishovite is very limited, with an average of 0.6 wt% TiO2 over the experimental P-T ranges. Lower oxygen fugacity decreases the solubility of SiO2 in rutile, whereas water has little effect on the solubility of SiO2 in rutile. Our experimental data are extreme useful for determine the depth of origin for the SiO2-bearing rutile in nature.
NASA Astrophysics Data System (ADS)
Zhang, Y.; Wu, Y.; WANG, C.; Jin, Z.
2015-12-01
Large-scale oceanic/continental subduction introduces a range of crustal materials into the Earth's mantle. These subducted material will be gravitationally trapped in the deep mantle when they have been transported to a depth of greater than ~250-300 km ("depth of no return"). However, little is known about the fate of these trapped continental material. Here, we conduct experimental study on a natural continental rock which compositionally similar to the average upper continental crust (UCC) over a pressure and temperature range of 9-16 GPa and 1300-1800 oC to constraint the fate of these trapped continental materials. The experimental results demonstrate that subducted UCC produces ~20-30 wt% K-rich melt (>55 wt% SiO2) in the upper mantle (9-13 GPa). The melting residue is mainly composed of coesite/stishovite + clinopyroxene + kyanite. In contrast, partial melting of subducted UCC in the MTZ produces ~10 wt% K-rich melt (<50 wt% SiO2), together with stishovite, clinopyroxene, K-Hollandite, garnet and CAS-phase as the residue phases. The melting residue phases achieve densities greater than the surrounding mantle, which provides a driving force for descending across the 410 km seismic discontinuity into the MTZ. However, this density relationship is reversed at the base of MTZ, leaving the descended residues being accumulated above the 660 km seismic discontinuity and may contribute to the stagnated "second continent". On the other hand, the melt is ~0.3-0.7 g/cm3 less dense than the surrounding mantle and provides a buoyancy force for the ascending of melt to shallow depth. The ascending melt preserves a significant portion of the bulk-rock REEs and LILEs. Thus, chemical reaction between the melt and the surrounding mantle would leads to a variably metasomatised mantle. Re-melting of the metasomatised mantle may contribute to the origin of the "enriched mantle sources" (EM-sources). Therefore, through subduction, stagnation, partial melting and melt segregation of continental crust may create EM-sources and"second continent" at shallow depth and the base of the MTZ respectively, which may contribute to the observed geochemical/geophysical heterogeneity in Earth's interior.
NASA Astrophysics Data System (ADS)
Nagel, Thorsten; Düsterhöft, Erik; Schiffer, Christian
2017-04-01
We investigate the signature relevant mantle lithologies leave in the receiver function record for different adiabatic thermal gradients down to 800 kilometers depth. The parameter space is chosen to target the visibility of upwelling mantle (a plume). Seismic velocities for depleted mantle, primitive mantle, and three pyroxenites are extracted from thermodynamically calculated phases diagrams, which also provide the adiabatic decompression paths. Results suggest that compositional variations, i.e. the presence or absence of considerable amounts of pyroxenites in primitive mantle should produce a clear footprint while horizontal differences in thermal gradients for similar compositions might be more subtle. Peridotites best record the classic discontinuities at around 410 and 650 kilometers depth, which are associated with the olivin-wadsleyite and ringwoodite-perovskite transitions, respectively. Pyroxenites, instead, show the garnet-perovskite transition below 700 kilometers depth and SiO2-supersaturated compositions like MORB display the coesite-stishovite transition between 300 and 340 kilometers depth. The latter shows the strongest temperature-depth dependency of all significant transitions potentially allowing to infer information about the thermal state if the mantle contains a sufficient fraction of MORB-like compositions. For primitive and depleted mantle compositions, the olivin-wadsleyite transition shows a certain temperature-depth dependency reflected in slightly larger delay times for higher thermal gradients. The lower-upper-mantle discontinuity, however, is predicted to display larger delay times for higher thermal gradients although the associated assemblage transition occurs at shallower depths thus requiring a very careful depth migration if a thermal anomaly should be recognized. This counterintuitive behavior results from the downward replacement of the assemblage wadsleyite+garnet with the assemblage garnet+periclase at high temperatures. This transition causes even lower seismic velocities with greater depth (following an adiabatic gradient), the highly continuous nature of the reaction, however, should produce only a smooth negative conversion. In contrast, a small positive conversion is expected at normal thermal gradients in the same depth range between 500 and 550 kilometers because of the wadsleyite-ringwoodite-transition. Hence, the polarity of the 520 discontinuity also offers a possibility to recognize the thermal state of the upper mantle.
Introduction to the structures and processes of subduction zones
NASA Astrophysics Data System (ADS)
Zheng, Yong-Fei; Zhao, Zi-Fu
2017-09-01
Subduction zones have been the focus of many studies since the advent of plate tectonics in 1960s. Workings within subduction zones beneath volcanic arcs have been of particular interest because they prime the source of arc magmas. The results from magmatic products have been used to decipher the structures and processes of subduction zones. In doing so, many progresses have been made on modern oceanic subduction zones, but less progresses on ancient oceanic subduction zones. On the other hand, continental subduction zones have been studied since findings of coesite in metamorphic rocks of supracrustal origin in 1980s. It turns out that high-pressure to ultrahigh-pressure metamorphic rocks in collisional orogens provide a direct target to investigate the tectonism of subduction zones, whereas oceanic and continental arc volcanic rocks in accretionary orogens provide an indirect target to investigate the geochemistry of subduction zones. Nevertheless, metamorphic dehydration and partial melting at high-pressure to ultrahigh-pressure conditions are tectonically applicable to subduction zone processes at forearc to subarc depths, and crustal metasomatism is the physicochemical mechanism for geochemical transfer from the slab to the mantle in subduction channels. Taken together, these provide us with an excellent opportunity to find how the metamorphic, metasomatic and magmatic products are a function of the structures and processes in both oceanic and continental subduction zones. Because of the change in the thermal structures of subduction zones, different styles of metamorphism, metasomatism and magmatism are produced at convergent plate margins. In addition, juvenile and ancient crustal rocks have often suffered reworking in episodes independent of either accretionary or collisional orogeny, leading to continental rifting metamorphism and thus rifting orogeny for mountain building in intracontinental settings. This brings complexity to distinguish the syn-subduction processes and products from post-subduction processes and products. Nevertheless, available results indicate that our definition and understanding of subduction zone processes and products can be advanced by the convergence of observations and interpretations from geochemical, geological, geophysical and geodynamic studies of both oceanic and continental subduction zones. Therefore, insights into subduction zones can be provided by intergration of different approaches from different targets in the near future.
NASA Astrophysics Data System (ADS)
Zhu, Jianjiang; Zhang, Lifei; Lü, Zeng; Bader, Thomas
2018-03-01
Subduction zones are important for understanding of the global carbon cycle from the surface to deep part of the mantle. The processes involved the metamorphism of carbonate-bearing rocks largely control the fate of carbon and contribute to local carbon isotopic heterogeneities of the mantle. In this study, we present petrological and geochemical results for marbles and carbonated eclogites in the Southwestern Tianshan UHP belt, NW China. Marbles are interlayered with coesite-bearing pelitic schists, and have Sr-Nd isotopic values (εNd (T=320Ma) = -3.7 to -8.9, 87Sr/86Sr (i) = 0.7084-0.7089), typical of marine carbonates. The marbles have dispersed low δ18OVSMOW values (ranging from 14 to 29‰) and unaffected carbon isotope (δ13CVPDB = -0.2-3.6‰), possibly due to infiltration of external H2O-rich fluids. Recycling of these marbles into mantle may play a key role in the carbon budget and contributed to the mantle carbon isotope heterogeneity. The carbonated eclogites have high Sr isotopic compositions (87Sr/86Sr (i) = 0.7077-0.7082) and positive εNd (T = 320 Ma) values (from 7.6 to 8.2), indicative of strong seafloor alteration of their protolith. The carbonates in the carbonated eclogites are mainly dolomite (Fe# = 12-43, Fe# = Fe2+/(Fe2+ + Mg)) that were added into oceanic basalts during seafloor alteration and experienced calcite - dolomite - magnesite transformation during the subduction metamorphic process. The uniformly low δ18O values (∼11.44‰) of carbonates in the carbontaed eclogites can be explained by closed-system equilibrium between carbonate and silicate minerals. The low δ13C values (from -3.3 to -7.7‰) of the carbonated eclogites most likely reflect contribution from organic carbon. Recycling of these carbonated eclogites with C isotope similar to typical mantle reservoirs into mantle may have little effect on the mantle carbon isotope heterogeneity.
Regional metamorphism at extreme conditions: Implications for orogeny at convergent plate margins
NASA Astrophysics Data System (ADS)
Zheng, Yong-Fei; Chen, Ren-Xu
2017-09-01
Regional metamorphism at extreme conditions refers either to Alpine-type metamorphism at low geothermal gradients of <10 °C/km, or to Buchan-type metamorphism at high geothermal gradients of >30 °C/km. Extreme pressures refer to those above the polymorphic transition of quartz to coesite, so that ultrahigh-pressure (UHP) eclogite-facies metamorphism occurs at mantle depths of >80 km. Extreme temperatures refer to those higher than 900 °C at crustal depths of ≤80 km, so that ultrahigh-temperature (UHT) granulite-facies metamorphism occurs at medium to high pressures. While crustal subduction at the low geothermal gradients results in blueschist-eclogite facies series without arc volcanism, heating of the thinned orogenic lithosphere brings about the high geothermal gradients for amphibolite-granulite facies series with abundant magmatism. Therefore, UHP metamorphic rocks result from cold lithospheric subduction to the mantle depths, whereas UHT metamorphic rocks are produced by hot underplating of the asthenospheric mantle at the crustal depths. Active continental rifting is developed on the thinned lithosphere in response to asthenospheric upwelling, and this tectonism is suggested as a feasible mechanism for regional granulite-facies metamorphism, with the maximum temperature depending on the extent to which the mantle lithosphere is thinned prior to the rifting. While lithospheric compression is associated with subduction metamorphism in accretionary and collisional orogens, the thinned orogenic lithosphere undergoes extension due to the asthenospheric upwelling to result in orogen-parallel rifting metamorphism and magmatism. Thus, the rifting metamorphism provides a complement to the subduction metamorphism and its operation marks the asthenospheric heating of the orogenic lithosphere. Because of the partial melting and melt extraction of the lower continental crust, contemporaneous granite-migmatite-granulite associations may serve as a petrological indicator of rifting orogeny that is superimposed on precedingly accretionary and collisional orogens. The UHT metamorphic rocks have occurred since the Archean, suggesting that the hot underplating has operated very early in the Earth's history. In contrast, the UHP metamorphic rocks primarily occur in the Phanerozoic, indicating that the thermal regime of many subduction zones has changed since the Neoproterozoic for the cold subduction.
A petro-structural review of the Zermatt-Saas Fee zone
NASA Astrophysics Data System (ADS)
Schenker, Filippo Luca; Markus Schmalholz, Stefan; Baumgartner, Lukas
2014-05-01
The Zermatt-Saas Fee zone (ZSZ) is an imbricate of fragments of blueschist- to eclogite-facies metabasalts and metagabbros, serpentinites and mélange zones containing blocks of the above mentioned rocks. The ZSZ is usually interpreted as a fragment of oceanic crust belonging to the Piemont-Ligurian (Tethyan) Ocean that was accreted into the Alpine nappe pile. In the last decades the discovery of several Ultra-High Pressure (UHP, >2.7 GPa at 550-600 °C from coesite bearing eclogites and diamond-bearing fluid inclusions in garnet) localities lead to the interpretation of deep subduction (> 100 km) of the ZSZ in the Eocene, and subsequent uplift from mantle depth with high exhumation rates (e.g. Amato et al., 1999). However, these high pressures are in apparent contrast to the regional metamorphic conditions that reflect pressures peaking at < 2 GPa for 550-600°C (blueschist and eclogite mineral assemblages in mafic rocks). These latter metamorphic conditions do not need anomalous high burial histories and exhumation velocities higher than the plate velocities. The magnitude and distribution of pressure in the tectonic units of the ZSZ are important for constraining dynamic models for the evolution of the ZSZ and the Western Alps. Before entering into dynamic models, we propose a petro-structural overview where the published petrological data on pressure and temperature are critically reviewed, and positioned on a geological map and cross section in order to integrate them into the proper structural and tectonic framework. The questions we seek to answer are: How is the pressure distributed within the main tectonic units and within the entire ZSZ? Do we observe sharp or gradual pressure gradients within the ZSZ? Can the UHP conditions be averaged/extended to the entire ZSZ? If not, do they correspond to conditions of observable subunits, or do they reflect anomalies in the pressure field? Answering these questions is fundamental to better understand the thermobarometric evolution patterns of the ZSZ, to properly evaluate the geodynamic mechanism of accretion of oceanic crust into orogens, and to better understand the formation of tectonic nappes in general.
Serpentinite-driven Exhumation of the UHP Lago di Cignana Unit in the Fossil Alpine Plate Interface
NASA Astrophysics Data System (ADS)
Scambelluri, M.; Gilio, M.; Angiboust, S.; Godard, M.; Pettke, T.
2015-12-01
The Lago di Cignana Unit (LCU) is a coesite- [1] and diamond-bearing [2] slice of oceanic-derived eclogites and metasediments recording Alpine UHP metamorphism at 600 °C-3.2 GPa (~110 km depth) [3]. The LCU is tectonically sandwiched between the eclogitic Zermatt-Saas Zone (ZSZ; 540 °C-3.2 GPa) [4] and the blueschist Combin Zone (400 °C-0.9 GPa) [5] along a tectonic structure joining HP units recording a ~1.2 GPa (40 km) pressure difference. So far, the ZSZ has been attributed to normal HP conditions and the mechanism driving exhumation and accretion of the LCU in its present structural position is not fully understood.We performed petrography and bulk-rock trace element analyses of rocks from LCU and ZSZ serpentinites. We observed that, while serpentinites in the core of the ZSZ show normal subduction zone trace elements and REE's patterns, the Ol+Ti-chu+Chl veins and host serpentinites enveloping the LCU are strongly enriched in sediment-derived fluid-mobile elements (U, Th, Nb, Ta, Ce, Y, As, Sb) and REE's: their patterns well match those of the closely associated LCU-UHP rocks.The presence of extremely enriched Ol+Ti-chu+Chl veins in the serpentinites at direct contact with the UHP Lago di Cignana Unit suggests that fluid exchange between serpentinite and LCU crustal rocks occurred at peak metamorphic conditions. Their coupling therefore occurred during subduction burial and/or peak UHP conditions. As such, the buoyancy force originating from the relatively light serpentinites fuelled the exhumation of the Lago di Cignana Unit. In this contest, the tectonic contact between the Zermatt-Saas Zone and the Combin Zone evolved into a true tectonic plate interface surface.1. Reinecke (1998). Lithos 42(3), 147-189; 2. Frezzotti et al. (2011). Nat. Geosci. 4(10), 703-706; 3. Groppo et al. (2009). J. Metam. Geol. 27(3), 207-231; 4. Angiboust et al. (2009). Terra Nova 21(3), 171-180; 5. Reddy et al. (1999). J. Metam. Geol. 17, 573-590.
Introduction to the structures and processes of subduction zones
NASA Astrophysics Data System (ADS)
Zheng, Yong-Fei; Zhao, Zi-Fu
2017-09-01
Subduction zones have been the focus of many studies since the advent of plate tectonics in 1960s. Workings within subduction zones beneath volcanic arcs have been of particular interest because they prime the source of arc magmas. The results from magmatic products have been used to decipher the structures and processes of subduction zones. In doing so, many progresses have been made on modern oceanic subduction zones, but less progresses on ancient oceanic subduction zones. On the other hand, continental subduction zones have been studied since findings of coesite in metamorphic rocks of supracrustal origin in 1980s. It turns out that high-pressure to ultrahigh-pressure metamorphic rocks in collisional orogens provide a direct target to investigate the tectonism of subduction zones, whereas oceanic and continental arc volcanic rocks in accretionary orogens provide an indirect target to investigate the geochemistry of subduction zones. Nevertheless, metamorphic dehydration and partial melting at high-pressure to ultrahigh-pressure conditions are tectonically applicable to subduction zone processes at forearc to subarc depths, and crustal metasomatism is the physicochemical mechanism for geochemical transfer from the slab to the mantle in subduction channels. Taken together, these provide us with an excellent opportunity to find how the metamorphic, metasomatic and magmatic products are a function of the structures and processes in both oceanic and continental subduction zones. Because of the change in the thermal structures of subduction zones, different styles of metamorphism, metasomatism and magmatism are produced at convergent plate margins. In addition, juvenile and ancient crustal rocks have often suffered reworking in episodes independent of either accretionary or collisional orogeny, leading to continental rifting metamorphism and thus rifting orogeny for mountain building in intracontinental settings. This brings complexity to distinguish the syn-subduction processes and products from post-subduction processes and products. Nevertheless, available results indicate that our definition and understanding of subduction zone processes and products can be advanced by the convergence of observations and interpretations from geochemical, geological, geophysical and geodynamic studies of both oceanic and continental subduction zones. Therefore, insights into subduction zones can be provided by integration of different approaches from different targets in the near future.
NASA Astrophysics Data System (ADS)
Stagno, Vincenzo; Bindi, Luca; Steinhardt, Paul J.; Fei, Yingwei
2017-10-01
Two of the three natural quasiperiodic crystals found in the Khatyrka meteorite show a composition within the Al-Cu-Fe system. Icosahedrite, with formula Al63Cu24Fe13, coexists with the new Al62Cu31Fe7 quasicrystal plus additional Al-metallic minerals such as stolperite (AlCu), kryachkoite [(Al,Cu)6(Fe,Cu)], hollisterite (AlFe3), khatyrkite (Al2Cu) and cupalite (AlCu), associated to high-pressure phases like ringwoodite/ahrensite, coesite, and stishovite. These high-pressure minerals represent the evidence that most of the Khatyrka meteoritic fragments formed at least at 5 GPa and 1200 °C, if not at more extreme conditions. On the other hand, experimental studies on phase equilibria within the representative Al-Cu-Fe system appear mostly limited to ambient pressure conditions, yet. This makes the interpretation of the coexisting mineral phases in the meteoritic sample quite difficult. We performed experiments at 3, 5 and 21 GPa and temperatures of 800-1500 °C using the multi-anvil apparatus to investigate the phase equilibria in the Al65Cu23Fe12 system representative of the first natural quasicrystal, icosahedrite. Our results, supported by single-crystal X-ray diffraction and analyses by scanning electron microscopy, confirm the stability of icosahedrite at high pressure and temperature along with additional coexisting Al-bearing phases representative of khatyrkite and stolperite as those found in the natural meteorite. One reversal experiment performed at 5 GPa and 1200 °C shows the formation of the icosahedral quasicrystal from a pure Al, Cu and Fe mixture, a first experimental synthesis of icosahedrite under those conditions. Pressure appears to not play a major role in the distribution of Al, Cu and Fe between the coexisting phases, icosahedrite in particular. Results from this study extend our knowledge on the stability of icosahedral AlCuFe at higher temperature and pressure than previously examined, and provide a new constraint on the stability of icosahedrite.
NASA Astrophysics Data System (ADS)
Zheng, Yong-Fei; Fu, Bin; Gong, Bing; Li, Long
2003-07-01
Discovery of coesite, diamond, and extreme 18O-depletion in eclogites from the Dabie-Sulu orogen in central-east China has contributed much to our understanding of subduction of continental crust to mantle depths and its subsequent exhumation. Hydrogen, oxygen, and carbon isotope distributions were systematically investigated in the past 8 years for ultrahigh pressure (UHP) eclogites, gneisses, granulites, marbles, and peridotites from this exciting region. The available data show the following characteristic features: (1) variable δ18O values of -11‰ to +10‰ for the eclogites and gneisses, with both equilibrium and disequilibrium fractionations of oxygen isotopes among minerals; (2) disequilibrium fractionation of hydrogen isotopes between mica and epidote from both eclogites and gneisses, with low δD values up to -127‰ to -100‰ for phengite; (3) negative δ13C values of -28‰ to -21‰ for apatite as well as host-eclogites and gneisses; (4) positive δ13C values of +1‰ to +6‰ for coesite-bearing marble associated with eclogites; (5) zircons from metamorphic rocks of different grades show a large variation in δ18O from -11‰ to +9‰, with U-Pb ages of 700 to 800 Ma for the timing of low- δ18O magma crystallization. It appears that the UHP metamorphic rocks exhibit ranges of δ18O values that are typical of potential precursor protolith rocks. Preservation of the oxygen isotope equilibrium fractionations among the minerals of the UHP eclogites and gneisses suggests that these rocks acquired the low δ18O values by meteoric-hydrothermal alteration before the UHP metamorphism. Thus, the UHP metamorphic rocks largely reflect the δ18O values of their premetamorphic igneous or sedimentary precursors. The stable isotope data demonstrate that basaltic, granitic, and sedimentary protoliths of the eclogites, orthogneiss, and paragneiss in the orogen were at or near the earth's surface, and subjected to varying degrees of water-rock interaction at some time before plate subduction. The low- δ18O rocks were isolated from water-rock interactions during their descent to and return from mantle depths. It appears that the oxygen, hydrogen, and carbon on the earth's surface were recycled into the mantle at depths of >200 km by the continental subduction. A fried ice cream model is advanced as an analogy to the rapid processes of both plate subduction and exhumation, with a short residence time of the UHP slab at mantle depths. The entire cycle of subduction, UHP metamorphism, and exhumation is estimated to take place in about 10 to 20 Ma. The 18O-depleted zircons and other minerals acquired their oxygen isotope compositions from low- δ18O magmas that incorporated the isotopic signatures of meteoric water in rifting tectonic zones prior to solidification. The U-Pb discordia dating for the 18O-depleted zircons revealed that the meteoric water-rock interaction occurred at Neoproterozoic, a time being much earlier than the UHP metamorphism at Triassic, but correlated with the Rodinian breakup, positive carbon isotope anomaly in carbonates, and the snowball earth event. The unusually low δ18O values can be acquired from either the meteoric water of cold paleoclimates or the melt water of glacial ice or snow. Neoproterozoic rift magmatism along the northern margin of the Yangtze craton may have provided sufficient heat source to trigger the meteoric-hydrothermal circulation. It is possible that the unusual 18O-depletion in the meta-igneous rocks occurs at some time prior to the snowball earth event, when there is a transition from a very cold earth with continental glaciers to a widely glaciated earth where bulk of the earth is covered by sea ice as defined for the snowball earth. The heterogeneity of oxygen isotope compositions at outcrop scales demonstrates the absence of pervasive fluid infiltration during prograde, peak UHP, and retrograde metamorphism; most rocks appear to have recrystallized under virtually closed system conditions characterized by widespread lack of an aqueous fluid phase. Volatiles may not escape from the rock series during the rapid subduction of the continental crust, resulting in a general lack of syn-collisional arc-magmatism in this orogen. Big differences in pressure and time from the peak UHP stage to the retrograde HP eclogite-facies stage cause significant release of aqueous fluid by dehydration from decompressing slabs during exhumation. As a result, fluid flow occurred in a channellized way on small scales subsequent to the UHP metamorphism, with very limited mobility of fluid at peak UHP conditions. The fluid for retrograde reactions was internally buffered in stable isotope compositions. While some fluids were locally derived from the surrounding gneisses, more fluid was probably derived from internal dehydration of the rock units in question. In addition to the breakdown of hydroxyl-bearing minerals, exsolution of structural hydroxyl dissolved in nominally anhydrous minerals due to abrupt decrease in pressure may have been an important source for the retrograde fluid.
NASA Astrophysics Data System (ADS)
Dutta, D.; Mukherjee, S.
2017-12-01
Coesite-bearing eclogites from the Tso Morari Dome (TMD) and the Kaghan valley (Pakistan) are two examples from the Himalayan orogen that attained UHP conditions within 5 Ma, by subducting the frontal part of the advancing Indian plate through a subduction channel, and subsequently extruded rapidly ( 17 mm yr-1). This study focuses on the deformation of the gneissic rock that hosts the UHP eclogites. 25 rock samples were collected from two transects viz. (A) Sumdo-Karzok and (B) Sumdo-Debring. Preliminary thin-section studies reveal differences in microstructural characters between the rocks of A and B. Although dynamically recrystallised quartz grains are present in all these samples, grain boundary migration recyrstallisation ( 530-650 °C) are better preserved in the rocks of A. Similarly, intra-granular fractures in both quartz and feldspars, the latter being dominant, are more prominent in the samples along A. Chessboard extinction patterns (> 700 °C) in quartz, micro-faults in plagioclase grains and undulatory extinction in micas are also present. Samples close to the Zildat shear zone (ZSZ; N margin of the TMD) exhibit medium-sized, lenticular quartzo-feldspathic grains. Their abundance wanes away from the fault possibly due to decreasing deformation intensity. XRD studies reveal a decline in the ratio of modal percentage K-feldspar to that of muscovite towards the N margin: the fall being more gradual along B. Biotites are less abundant (< 1%) in the samples near the ZSZ, but the total content of phyllosilicates (Ms+Bt+Chl) show a rise of > 14 % towards the ZSZ. Previous workers reported similar increase in micaceous minerals in ductile- and brittle shear zones from other terrains, and suggested higher fluid activity as the key factor. Subduction of the Indian continental crust and subsequent exhumation, along the subduction channel, followed Coutte- and Poiseuille flows, respectively. Hence, rocks near the ZSZ should exhibit opposing shear senses, which we encounter both at micro- and meso-scales. Besides, Google Earth images show geomorphologic features viz. displaced NW trending ridges, linear lake margins etc., which probably indicate regional scale (neotectonic?) NNW trending strike-slip. This can also explain the origin of the nearby major lakes viz. Tso Moriri, Tso Kar and Kiagar Tso.
Diamond and Unusual Minerals Discovered from the Chromitite in Polar Ural: A First Report
NASA Astrophysics Data System (ADS)
Yang, J.; Bai, W.; Fang, Q.; Meng, F.; Chen, S.; Zhang, Z.
2007-12-01
Ultrahigh pressure (UHP) minerals, such as diamond, coesite, and pseudomorphs of octahedral olivine, and as well as about 80 other mineral species have been recovered from podiform chromitites of the Luobusa ophiolite, southern Tibet, and a new mineral, Luobusaite (Fe0.82Si2), has been approved recently by CNMMN. The UHP minerals from Luobusa are controversial because they have not found in situ and because ophiolites are currently believed to form at shallow levels above oceanic spreading centers. More detailed study and experimental work are needed to understand the origin and significance of these unusual minerals and investigations of other ophiolites are needed to determine if such minerals occur elsewhere. For this purpose, we collected about 1500 kg of chromitite from two orebodies in an ultramafic body in the Polar Urals. Thus far, more than 60 different mineral species have been separated from these ores. The most exciting discovery is the common occurrence of diamond, a typical UHP mineral in the Luobusa chromitites. Diamonds from Ural chromitite are clear, colorless, well-developed crystals with octahedral morphology, generally 0.2-0.3 mm in size. Attached with the diamonds and perhaps also occurring as inclusions within them are many minerals as chromite, MnNiCrFe alloy, native Si and Ta, corundum, zircon, feldspar, garnet, moissanite, confirming their natural origin and suggesting a long residence time in the mantle. Other mineral group include: (1) native elements: Cr, W, Ni, Co, Si, Al and Ta; (2) carbides: SiC and WC; (3) alloys: Cr-Fe, Si-Al-Fe, Ni-Cu, Ag-Au, Ag-Sn, Fe-Si, Fe-P, and Ag-Zn-Sn; (4) oxides: NiCrFe, PbSn, REE, rutile and Si- bearing rutile, ilmenite, corundum, chromite, MgO, and SnO2; (5) silicates: kyanite, pseudomorphs of octahedral olivine, zircon, garnet, feldspar, and quartz,; (6) sulfides of Fe, Ni, Cu, Mo, Pb, Ab, AsFe, FeNi, CuZn, and CoFeNi; and (7) iron groups: native Fe, FeO, and Fe2O3. These minerals are very similar in composition and structure to those reported from the Luobusa chromitites. For examples, some spherules of native iron contain spherical inclusions of FeO, exactly like comparable grains in the Luobusa sample.
NASA Astrophysics Data System (ADS)
Ashchepkov, I.; Vladykin, N.; Mitchell, R.; Coopersmith, H.; Garanin, V.; Saprykin, A. I.; Khmelnikova, O. S.
Mineral grains and their intergrowth from the concentrate form the KL1- kimberlite pipe Colorado plateau was analyzed by EPMA and LAM ICP MS in Analytic Center of UIGGM. Garnets reveal nearly continuous trend of the compositions divided into 5 intervals. 1 cumulates from the crust and Sp facie mantle; 2. Gar-Sp lherzolites; 3- Gar- wehrlites, lherzolites and harzburgites; 4- Gar lherzolites and harzburgites; 4. Pyroxenites and Il peri-dotites . They reveal three trend of Ti decrease with the ris- ing Cr content. Those in the inter-growth with the pyroxenes are less in Tio2 as well as the pyroxenes. Discrete large Cpx grains are richer in Na, Al, Cr. TP conditions determined for the clinopyroxenes with Nimis- Taylor, 2001 thermobarometer and barometer Ashchepkov, 2001 reveal the heating from 35 to 40-42 mv/m2 in 30-50kbar interval. The spinels show two compositional intervals 64-50% Cr2O3 and 47-30%. The branch with the essential enrichment to 8% TiO2with the Cr decrease what also suppose the peridotite alteration due to rising of evolving Ti-rich melts. Two descend- ing crystallization lines for the ilmenites suggest the (polybaric) differentiation in two magmatic chambers. The Cr-rich ilmenites and most Cr-rich subcalcis garnets were found in the serpentinized ilmenite harzburgites that probably surround the most deep mag-matic chamber. The Ilm -Q (coesite) intergrowth suggests the deep differenti- ation. Several ilmenites contain up to 11%MnO. Trace elements determined for the clinopyroxenes suppose small decree melting possibly under influence of subducted- related melts having definite U peak and Ta-Nb minimums. Their reaction with peri- dotites with garnet dissolution according to AFC model decrease La/Ybn ration as well as the Pb* and U peak. Two stages of the Ti-rich melt percolations suggested to be accompanied the plum- re-lated melts influence on the peridotite of Wyoming craton keel which was followed with fur-ther followed by submelting of the subducted essentially eclogitic Na-Ti material. The de-formations assist the melt percolation at the final stage. Supported by RBEF grants 05-99-65688, 00-05-65288
Separate zones of sulfate and sulfide release from subducted mafic oceanic crust
NASA Astrophysics Data System (ADS)
Tomkins, Andrew G.; Evans, Katy A.
2015-10-01
Liberation of fluids during subduction of oceanic crust is thought to transfer sulfur into the overlying sub-arc mantle. However, despite the importance of sulfur cycling through magmatic arcs to climate change, magma oxidation and ore formation, there has been little investigation of the metamorphic reactions responsible for sulfur release from subducting slabs. Here, we investigate the relative stability of anhydrite (CaSO4) and pyrite (FeS2) in subducted basaltic oceanic crust, the largest contributor to the subducted sulfur budget, to place constraints on the processes controlling sulfur release. Our analysis of anhydrite stability at high pressures suggests that this mineral should dominantly dissolve into metamorphic fluids released across the transition from blueschist to eclogite facies (∼450-650 °C), disappearing at lower temperatures on colder geothermal trajectories. In contrast, we suggest that sulfur release via conversion of pyrite to pyrrhotite occurs at temperatures above 750 °C. This higher temperature stability is indicated by the preservation of pyrite-bornite inclusions in coesite-bearing eclogites from the Sulu Belt in China, which reached temperatures of at least 750 °C. Thus, sulfur may be released from subducting slabs in two separate pulses; (1) varying proportions of SO2, HSO4- and H2S are released via anhydrite breakdown at the blueschist-eclogite transition, promoting oxidation of remaining silicates in some domains, and (2) H2S is released via pyrite breakdown well into the eclogite facies, which may in some circumstances coincide with slab melting or supercritical liquid generation driven by influx of serpentinite-derived fluids. These results imply that the metallogenic potential in the sub-arc mantle above the subducting slab varies as a function of subduction depth, having the greatest potential above the blueschist-eclogite transition given the association between oxidised magmas and porphyry Cu(-Au-Mo) deposits. We speculate that this zoned sulfur liberation might be one of the factors that lead to the apparently redox-influenced zoned distribution of ore deposit types in the Andean arc. Furthermore, given the lack of sulfate-associated sea floor oxidation prior to the second great oxidation event, the pattern of sulfur transfer from the slab to the sub-arc mantle likely changed over time, becoming shallower and more oxidised from the Neoproterozoic onwards.
NASA Astrophysics Data System (ADS)
Liou, Juhn G.; Tsujimori, Tatsuki; Yang, Jingsui; Zhang, R. Y.; Ernst, W. G.
2014-12-01
Newly recognized occurrences of ultrahigh-pressure (UHP) minerals including diamonds in ultrahigh-temperature (UHT) felsic granulites of orogenic belts, in chromitites associated with ophiolitic complexes, and in mantle xenoliths suggest the recycling of crustal materials through deep subduction, mantle upwelling, and return to the Earth's surface. This circulation process is supported by crust-derived mineral inclusions in deep-seated zircons, chromites, and diamonds from collision-type orogens, from eclogitic xenoliths in kimberlites, and from chromitities of several Alpine-Himalayan and Polar Ural ophiolites; some of these minerals contain low-atomic number elements typified by crustal isotopic signatures. Ophiolite-type diamonds in placer deposits and as inclusions in chromitites together with numerous highly reduced minerals and alloys appear to have formed near the mantle transition zone. In addition to ringwoodite and inferred stishovite, a number of nanometric minerals have been identified as inclusions employing state-of-the-art analytical tools. Reconstitution of now-exsolved precursor UHP phases and recognition of subtle decompression microstructures produced during exhumation reflect earlier UHP conditions. For example, Tibetan chromites containing exsolution lamellae of coesite + diopside suggest that the original chromitites formed at P > 9-10 GPa at depths of >250-300 km. The precursor phase most likely had a Ca-ferrite or a Ca-titanite structure; both are polymorphs of chromite and (at 2000 °C) would have formed at minimum pressures of P > 12.5 or 20 GPa respectively. Some podiform chromitites and host peridotites contain rare minerals of undoubted crustal origin, including zircon, feldspars, garnet, kyanite, andalusite, quartz, and rutile; the zircons possess much older U-Pb ages than the time of ophiolite formation. These UHP mineral-bearing chromitite hosts evidently had a deep-seated evolution prior to extensional mantle upwelling and partial melting at shallow depths to form the overlying ophiolite complexes. These new findings together with stable isotopic and inclusion characteristics of diamonds provide compelling evidence for profound underflow of both oceanic and continental lithosphere, recycling of surface 'organic' carbon into the lower mantle, and ascent to the Earth's surface through mantle upwelling. Intensified study of UHP granulite-facies lower crustal basement and ophiolitic chromitites should allow a better understanding of the geodynamics of subduction and crustal cycling.
NASA Astrophysics Data System (ADS)
Li, H.; Jahn, B.; Wang, D.; Yu, H.; Liu, Z.; Hou, G.
2013-12-01
As the largest coesite-bearing mafic-ultramafic body in the Dabie-Sulu orogen, the Bixiling Complex is composed of meta-ultramafic rocks, MgAl-rich eclogites and FeTi-rich eclogites. The FeTi-rich eclogites are further divided into low-Si-high-Fe type (Type I) and high-Si-low-Fe type (Type II) according to their mineral assemblages and bulk chemical composition. Field, petrographic, petrological and geochemical characteristics of these rocks, although suffered an ultra-high pressure metamorphism, still show a magmatic differentiation process among the protoliths of the meta-ultramafic rocks, MgAl-rich eclogites and Type I FeTi-rich eclogites. A small degree of lower crustal contamination occurred during their magma chamber process. Amphibolite is widespread in the periphery of the complex. Non-foliation and fine-grained texture are their obvious characteristics. Geochemical and isotopic affinities suggest that the amphibolites represent a product of complete retrogression from type II FeTi-rich eclogites. The UHP complex is enclosed in granitic gneisses, which variably include two-mica plagioclase gneiss, epidote two-mica plagioclase gneiss, or white-mica plagioclase gneiss. They all show TTG, especially trondjhemitic composition. A migmatite outcrop was found near the northeastern end of the complex. The migmatites consist of dark colored, non-foliated amphibolites and light-colored, fine-grained trondhjemitic gneisses. Field occurrences, microstructures observed under optical microscope and SEM, Sr-Nd isotopic data suggest an origin of partial melting. Chemical composition of two stages of amphiboles occurred in both the amphibolites and the trondhjemitic gneisses also imply a partial melting process occurred. Trace element, Sr-Nd isotope and SHRIMP zircon U-Pb dating of MgAl-rich eclogite, amphibolites and trondhjemite suggest that the migmatites represent a partial melting of crustal materials at about 780Ma, possibly accompanied by the coeval emplacement of a differentiated mafic intrusive body. These rocks were deeply subducted into a mantle depth during the Triassic continental collision between the Yangtze Craton and North China Craton, and thereafter were exhumed to the surface. Their residual geochemical characteristics and spatial / temporal relationship could impose constraints on the tectonic evolution of the Dabieshan UHP terrane.
NASA Astrophysics Data System (ADS)
Gibbs, G. V.; Cox, D. F.; Ross, N. L.
Employing first-principles methods, the docking sites for H were determined and H, Al, and vacancy defects were modeled with an infinite periodic array of super unit cells each consisting of 27 contiguous symmetry nonequivalent unit cells of the crystal structure of stishovite. A geometry optimization of the super-cell structure reproduces the observed bulk structure within the experimental error when P1 translational symmetry was assumed and an array of infinite extent was generated. A mapping of the valence electrons for the structure displays mushroom-shaped isosurfaces on the O atom, one on each side of the plane of the OSi3 triangle in the nonbonded region. An H atom, placed in a cell near the center of the super cell, was found to dock upon geometry optimization at a distance of 1.69 Å from the O atom with the OH vector oriented nearly perpendicular to the plane of the triangle such that the OH vector makes a angle of 91° with respect to [001]. However, an optimization of a super cell with an Al atom replacing Si and an H atom placed nearby in a centrally located cell resulted in an OH distance of 1.02 Å with the OH vector oriented perpendicular to [001] as observed in infrared studies. The geometry-optimized position of the H atom was found to be in close agreement with that (0.44, 0.12, 0.0) determined in an earlier study of the theoretical electron density distribution. The docking of the H atom at this site was found to be 330 kJ mol-1 more stable than a docking of the atom just off the shared OO edge of the octahedra as determined for rutile. A geometry optimization of a super cell with a missing Si generated a vacant octahedra that is 20% larger than that of the SiO6 octahedra. The valence electron density distribution displayed by the two-coordinate O atoms that coordinate the vacant octahedral site is very similar to those displayed by the bent SiOSi angles in coesite. The internal distortions induced by the defect were found to diminish rather rapidly with distance, with the structure annealing to that observed in the bulk crystal to within about three coordination spheres.
Geochronology of high-pressure granulites from the Czech part of the Zlote Unit (Bohemian Massif)
NASA Astrophysics Data System (ADS)
Lange, U.; Bröcker, M.; Trapp, E.
2003-04-01
At the NE margin of the Bohemian Massif, granulites occur in the Zlote Unit which is exposed in the border region between Poland and the Czech Republic [e.g. 1, 3]. On the Polish side, outcrop conditions are rather poor. Besides some isolated blocks, granulites are restricted to a very small occurrence near Stary Gieraltow. This exposure has attracted much attention due to findings of presumed coesite pseudomorphs, as inferred from radial fractures around polycrystalline quartz inclusions in garnet [1]. Peak metamorphic conditions were estimated between 21 and 28 kbar at 800 to 1000 °C [2]. Better outcrop conditions of the same tectonic unit are found on the Czech side in the Rychleby Mts [3]. The focus of this study is on the geochronology of granulites from this occurrence. By means of Sm-Nd (garnet, cpx, whole rock) and single grain U-Pb dating of zircon, we have studied felsic and mafic granulites collected near the location Cerveny Dul. A felsic granulite yielded a Sm-Nd age of 337 +/- 4 Ma (two grain-size fractions of garnet, whole rock). Two mafic granulites provided Sm-Nd ages (two grain-size fractions of garnet, cpx and/or whole rock) of 357 +/- 10 Ma and 351 +/- 10 Ma, respectively. The new Sm-Nd results are in good agreement with metamorphic ages reported for other Bohemian granulites and further document the significance of HP-HT metamorphism at c. 350-340 Ma. Single-grain zircon dating of air-abraded grains provided concordant results. Zircons from a mafic granulite yielded an age of 362 +/- 1 Ma. A similar result was reported for a mafic granulite from Stary Gieraltow, based on conventional multigrain analyses of zircon [2]. This age is considered to approximate the timing of crystallisation from a melt. However, it remains unclear whether this process took place before or during early stages of high-pressure metamorphism. The studied felsic granulite yielded a range in zircon ages between 390 to 330 Ma, indicating the presence of inherited magmatic grains and the influence of anatectic processes post-dating the pressure peak. [1] Bakun-Czubarow (1992): Arch. Mineral. 48, 3-25; [2] Klemd, R. &Bröcker, M. (1999): Contrib. Mineral. Petrol. 136, 358-373; [3] Pouba, Z., Padera, K. &Fiala, J. (1985): N. Jahrb. Mineral., Abh. 151, 29-52
Progressive Extensional Exhumation of the Ultrahigh-Pressure Tso Morari Terrain, NW Indian Himalaya
NASA Astrophysics Data System (ADS)
Hodges, K.; Clark, R.; Monteleone, B.; Sachan, H.; Mukherjee, B. K.; Ahmad, T.
2011-12-01
The core of the Tso Morari dome in the Ladakh region of NW India (roughly 33 °10'N; 78°10'E) is one of only two known ultrahigh-pressure (UHP) terrains in the Himalayan-Tibetan orogenic system. The quartzofeldspathic Puga Orthogneiss from the structurally deepest portions of the terrain does not contain UHP mineralogy but surrounds dismembered lenses of mafic eclogite with accessory coesite, confirming that at least the eclogite lenses experienced UHP metamorphic conditions (Mukherjee et al., 2003, International Geology Review; Sachan et al., 2004, European Journal of Mineralogy). U-Pb zircon dates from the Puga orthogneiss (53.3 ± 0.7 Ma: Leech et al., 2007, International Geology Review) provide what appear to be the most precise available constraints on the age of UHP metamorphism at Tso Morari provided we presume that the UHP assemblages in the eclogite lenses developed at the same time as the 53.3 ± 0.7 Ma metamorphic zircon in the orthogneiss. However, other components of the zircon population studied by Leech and co-workers, as well as the results obtained using other thermochronometers and geochronometers (de Sigoyer et al., 2004, Tectonics), demonstrate that a series of lower pressure metamorphic events also affected the Tso Morari terrain between ca. 53 Ma and ca. 45 Ma, implying rapid decompression at elevated temperatures (ca. 800 - 350°C). Our 1:50000-scale geologic mapping at Tso Morari provides evidence that this exhumation was largely accommodated by two previously unrecognized low-angle ductile detachments that separate the terrain into three tectonostratigraphic units with distinctive metamorphic histories. The structurally lowest shear zone (Karla detachment) separates the Puga Orthogneiss from overlying lower amphibolite facies metasedimentary rocks of the Zoboshisha Unit, which contains no UHP assemblages. Structurally higher and demonstrably younger detachments separate the Zoboshisha Unit and the Puga Orthogneiss from greenschist to epidote-amphibolite facies metasedimentary (and possibly metavolcanic) units of the Taglang La formation. The role of nested detachments in the early, rapid exhumation of UHP rocks at Tso Morari support a geodynamic model such as that of Chemenda and co-workers (1996, Earth and Planetary Science Letters) that involve extrusion of UHP terrains beneath rooted detachment systems. We suggest that synconvergence detachment systems can involve multiple generations of detachments that result in the progressive exhumation of UHP rocks over a brief period of time, a concept similar to that promoted by Johnston et al. (2007, Tectonics) for much slower, postconvergence exhumation of Norwegian UHP rocks.
Diamond and moissanite in ophiolitic mantle rocks and podiform chromitites: A deep carbon source?
NASA Astrophysics Data System (ADS)
Yang, J.; Xu, X.; Wiedenbeck, M.; Trumbull, R. B.; Robinson, P. T.
2010-12-01
Diamonds are known from a variety of occurreces, mainly from mantle-derived kimberlites, meteorite impact craters, and continental deep subduction and collision zones. Recently, an unusual mineral group was discovered in the Luobusa ophiolitic chromitites from the Yarlung Zangbu suture, Tibet, which probably originated from a depth of over 300 km in the mantle. Minerals of deep origin include coesite apparently pseudomorphing stishovite, and diamond as individual grains or inclusions in OsIr alloy. To determine if such UHP and unusual minerals occur elsewhere, we collected about 1.5 t of chromitite from two orebodies in an ultramafic body in the Polar Urals. Thus far, more than 60 different mineral species have been separated from these ores. The most exciting discovery is the common occurrence of diamond, a typical UHP mineral in the Luobusa chromitites. These minerals are very similar in composition and structure to those reported from the Luobusa chromitites. So far diamond and/or moissanite have been discovered from many different ophiolitic ultramafic rocks, including in-situ grains in polished chromitite fragments. These discoveries demonstrate that the Luobusa ophiolite is not a unique diamond-bearing massif. Secondary ion mass spectrometric (SIMS) analysis shows that the ophiolite-hosted diamond has a distinctive 13C-depleted isotopic composition (δ13C from -18 to -28‰, n=70), compatible to the ophiolite-hosted moissanite (δ13C from -18 to -35‰, n=36), both are much lighter than the main carbon reservoir in the upper mantle (δ13C near -5‰). The compiled data from moissanite from kimberlites and other mantle settings share the characteristic of strongly 13C-depleted isotopic composition. This suggests that diamond and moissanite originates from a separate carbon reservoir in the mantle or that its formation involved strong isotopic fractionation. Subduction of biogenic carbonaceous material could potentially satisfy both the unusual isotopic and redox constraints on diamond and moissanite formation, but this material would need to stay chemically isolated from the upper mantle until it reached the high-T stability field of diamond and moissanite. The origin of diamond and moissanite in the mantle is still unsolved, but all evidence from the upper mantle indicates that they cannot have formed there, except under special and local redox conditions. We suggest, alternatively, that diamond and moissanite may have formed in the lower mantle, where the existence of 13C-depleted carbon is strongly suspected.
The P-T-fO 2 stability of deerite, Fe{12/2+}Fe{6/3+}[Si12O40](OH)10
NASA Astrophysics Data System (ADS)
Lattard, Dominique; Le Breton, Nicole
1994-02-01
New equilibrium experiments have been performed in the 20 27 kbar range to determine the upper thermal stability limit of endmember deerite, Fe{12/2+}Fe{6/3+}[Si12O40](OH)10. In this pressure range, the maximum thermal stability limit is represented by the oxygen-conserving reaction: deerite(De)=9 ferrosilite(Fs)+3 magnetite(Mag)+3 quartz(Qtz)+5 H2O(W) (1). Under the oxygen fugacities of the Ni-NiO buffer the breakdown-reduction reaction: De=12 Fs+2 Mag+5 W+1/2 O2 (10) takes place at lower temperatures (e.g. ΔT=63° at 27 kbar). The experimental brackets can be fitted using thermodynamic data for ferrosilite, magnetite and quartz from Berman (1988) and the following 1 bar, 298 K data for deerite (per gfw): Vo=55.74 J.bar-1, So=1670 J.K-1, ΔH{f/o}=-18334 kJ, α=2.5x10-5K-1, β=-0.18x10-5 bar-1. Using these data in conjunction with literature data on coesite, grunerite, minnesotaite, and greenalite, the P-T stability field of endmember deerite has been calculated for P s= P H 2O. This field is limited by 6 univariant oxygenconserving dehydration curves, from which three have positive d P/d T slopes, the other three negative slopes. The lower pressure end of the stability field of endmember deerite is thus located at an invariant point at 250±70°C and 10+-1.5 kbar. Deerite rich in the endmember can thus appear only in environments with geothermal gradients lower than 10°C/km and at pressures higher than about 10 kbar, which is in agreement with 4 out of 5 independent P-T estimates for known occurrences. The presence of such deerite places good constraints on minimum pressure and maximum temperature conditions. From log f O 2- T diagrams constructed with the same data base at different pressures, it appears that endmember deerite is, at temperatures near those of its upper stability limit, stable only over a narrow range of oxygen fugacities within the magnetite field. With decreasing temperatures, deerite becomes stable towards slightly higher oxygen fugacities but reaches the hematite field only at temperatures more than 200°C lower than the upper stability limit. This practically precludes the coexistence deerite-hematite with near-endmember deerite in natural environments.
NASA Astrophysics Data System (ADS)
Tsuno, Kyusei; Dasgupta, Rajdeep
2011-05-01
We have experimentally investigated melting phase relation of a nominally anhydrous, carbonated pelitic eclogite (HPLC1) at 2.5 and 3.0 GPa at 900-1,350°C in order to constrain the cycling of sedimentary carbon in subduction zones. The starting composition HPLC1 (with 5 wt% bulk CO2) is a model composition, on a water-free basis, and is aimed to represent a mixture of 10 wt% pelagic carbonate unit and 90 wt% hemipelagic mud unit that enter the Central American trench. Sub-solidus assemblage comprises clinopyroxene + garnet + K-feldspar + quartz/coesite + rutile + calcio-ankerite/ankeritess. Solidus temperature is at 900-950°C at 2.5 GPa and at 900-1,000°C at 3.0 GPa, and the near-solidus melt is K-rich granitic. Crystalline carbonates persist only 50-100°C above the solidus and at temperatures above carbonate breakdown, carbon exists in the form of dissolved CO2 in silica-rich melts and as a vapor phase. The rhyodacitic to dacitic partial melt evolves from a K-rich composition at near-solidus condition to K-poor, and Na- and Ca-rich composition with increasing temperature. The low breakdown temperatures of crystalline carbonate in our study compared to those of recent studies on carbonated basaltic eclogite and peridotite owes to Fe-enrichment of carbonates in pelitic lithologies. However, the conditions of carbonate release in our study still remain higher than the modern depth-temperature trajectories of slab-mantle interface at sub-arc depths, suggesting that the release of sedimentary carbonates is unlikely in modern subduction zones. One possible scenario of carbonate release in modern subduction zones is the detachment and advection of sedimentary piles to hotter mantle wedge and consequent dissolution of carbonate in rhyodacitic partial melt. In the Paleo-NeoProterozoic Earth, on the other hand, the hotter slab-surface temperatures at subduction zones likely caused efficient liberation of carbon from subducting sedimentary carbonates. Deeply subducted carbonated sediments, similar to HPLC1, upon encountering a hotter mantle geotherm in the oceanic province can release carbon-bearing melts with high K2O, K2O/TiO2, and high silica, and can contribute to EM2-type ocean island basalts. Generation of EM2-type mantle end-member may also occur through metasomatism of mantle wedge by carbonated metapelite plume-derived partial melts.
Recycling of ancient subduction-modified mantle domains in the Purang ophiolite (southwestern Tibet)
NASA Astrophysics Data System (ADS)
Gong, Xiao-Han; Shi, Ren-Deng; Griffin, W. L.; Huang, Qi-Shuai; Xiong, Qing; Chen, Sheng-Sheng; Zhang, Ming; O'Reilly, Suzanne Y.
2016-10-01
Ophiolites in the Indus-Yarlung Zangbo (IYZ) suture (southern Tibet) have been interpreted as remnants of the Neo-Tethyan lithosphere. However, the discovery of diamonds and super-reducing, ultra-high pressure (SuR-UHP) mineral assemblages (e.g., coesite after stishovite, olivine after wadsleyite, native metals, alloys, and moissanite) in some of these massifs and associated chromitites requires a re-evaluation of their origin and evolution. A new petrological and geochemical study of the Purang ophiolite in the western IYZ suture sheds new lights on these issues. The depleted harzburgites of the Purang massif have low modal contents of clinopyroxene (< 2%), and high Cr# [100*Cr3 +/(Cr3 + + Al3 +)] in spinel (> 40 70) and pyroxenes (> 16 in orthopyroxene, and > 20 in clinopyroxene), suggesting high degrees of melt extraction (> 20%). These features are not consistent with formation in a (ultra-) slow-spreading mid-ocean ridge. These peridotites have high modal contents of orthopyroxene; this, and the extremely high Cr# of spinels in these peridotites, suggests modification in a subduction zone. The clinopyroxene-rich harzburgites and lherzolites contain rare spinel-pyroxene symplectites after garnet. Their clinopyroxenes have low MREE-to-HREE ratios ((Sm/Yb)N < 0.1) at relatively high HREE concentrations, and are Na-rich but Nd-poor. The relatively enrichment of Na but depletion of Nd in clinopyroxene cannot be explained by refertilization with MORB melts but are consistent with an origin from Na-rich subcontinental lithospheric mantle (SCLM). All lines of evidence suggest that these peridotites underwent initial melting in the stability field of garnet-facies peridotites, followed by additional melting in the spinel-facies mantle. Whole-rock Os isotopic compositions of the Purang peridotites give ancient TRD model ages (up to 1.3 Ga), indicating that the formation of these ancient depletion residues predated the opening of Neo-Tethyan Ocean. These observations, together with recent studies on other IYZ peridotites, suggest that the Purang peridotites are genetically unrelated to the associated mafic crust. Instead, they represent ancient SCLM domains, initially formed beneath a continental margin, and then modified by subduction, before they were incorporated into the Neo-Tethyan ocean basin. This model is consistent with the deep-mantle-recycling model for the presence of SuR-UHP phases in the IYZ ophiolites. The infiltration of MORB melts through these ancient depleted peridotites during their final exhumation in a (ultra-) slow-spreading center may have refertilized them to produce the clinopyroxene-rich peridotites.
NASA Astrophysics Data System (ADS)
Kueter, Nico; Soesilo, Joko; Fedortchouk, Yana; Nestola, Fabrizio; Belluco, Lorenzo; Troch, Juliana; Wälle, Markus; Guillong, Marcel; Von Quadt, Albrecht; Driesner, Thomas
2016-11-01
Diamonds in alluvial deposits in Southeast Asia are not accompanied by indicator minerals suggesting primary kimberlite or lamproite sources. The Meratus Mountains in Southeast Borneo (Province Kalimantan Selatan, Indonesia) provide the largest known deposit of these so-called "headless" diamond deposits. Proposals for the origin of Kalimantan diamonds include the adjacent Meratus ophiolite complex, ultra-high pressure (UHP) metamorphic terranes, obducted subcontinental lithospheric mantle and undiscovered kimberlite-type sources. Here we report results from detailed sediment provenance analysis of diamond-bearing Quaternary river channel material and from representative outcrops of the oldest known formations within the Alino Group, including the diamond-bearing Campanian-Maastrichtian Manunggul Formation. Optical examination of surfaces of diamonds collected from artisanal miners in the Meratus area (247 stones) and in West Borneo (Sanggau Area, Province Kalimantan Barat; 85 stones) points toward a classical kimberlite-type source for the majority of these diamonds. Some of the diamonds host mineral inclusions suitable for deep single-crystal X-ray diffraction investigation. We determined the depth of formation of two olivines, one coesite and one peridotitic garnet inclusion. Pressure of formation estimates for the peridotitic garnet at independently derived temperatures of 930-1250 °C are between 4.8 and 6.0 GPa. Sediment provenance analysis includes petrography coupled to analyses of detrital garnet and glaucophane. The compositions of these key minerals do not indicate kimberlite-derived material. By analyzing almost 1400 zircons for trace element concentrations with laser ablation ICP-MS (LA-ICP-MS) we tested the mineral's potential as an alternative kimberlite indicator. The screening ultimately resulted in a small subset of ten zircons with a kimberlitic affinity. Subsequent U-Pb dating resulting in Cretaceous ages plus a detailed chemical reflection make a kimberlitic origin unfavorable with respect to the regional geological history. Rather, trace elemental analyses (U, Th and Eu) suggest an eclogitic source for these zircons. The age distribution of detrital zircons allows in general a better understanding of collisional events that formed the Meratus orogen and identifies various North Australian Orogens as potential Pre-Mesozoic sediment sources. Our data support a model whereby the majority of Kalimantan diamonds were emplaced within the North Australian Craton by volcanic processes. Partly re-deposited into paleo-collectors or residing in their primary host, these diamond-deposits spread passively throughout Southeast Asia by terrane migration during the Gondwana breakup. Terrane amalgamation events largely metamorphosed these diamond-bearing lithologies while destroying the indicative mineral content. Orogenic uplift finally liberated their diamond-content into new, autochthonous placer deposits.
Dehydration and melting experiments constrain the fate of subducted sediments
NASA Astrophysics Data System (ADS)
Johnson, Marie C.; Plank, Terry
1999-12-01
Geochemical tracers demonstrate that elements are cycled from subducted sediments into the arc melting regime at subduction zones, although the transfer mechanism is poorly understood. Are key elements (Th, Be, Rb) lost during sediment dehydration or is sediment melting required? To investigate this question, we conducted phase equilibria and trace element partitioning experiments on a pelagic red clay for conditions appropriate to the slab beneath arc volcanoes (2-4 GPa, 600°-1000°C). Using both piston cylinders and multianvils, we determined the solidus, phase stabilities, and major element compositions of coexisting phases. The solidus (H2O + Cl fluid-saturated) was located at 775 +/- 25°C at 2 GPa, 810 +/- 15°C at 3 GPa, and 1025 +/- 25°C at 4 GPa with noevidence for complete miscibility between melt and fluid. This sediment composition produces a profusion of phases both above and below the solidus: garnet, jadeitic pyroxene, alkali-rich amphibole, phengite, biotite, magnetite, coesite, kyanite, apatite, zircon, Cl-rich fluids, and peraluminous to peralkaline granitic melts. At 2 GPa the phengite dehydration solidus is at 800°-825°C, while biotite breaks down between 850° and 900°C. To explore trace element partitioning across the solidus at 2 GPa, we used diamonds to trap fluids and melts. Both the bulk sediment residues and diamond traps were analyzed postexperiment by inductively coupled plasma-mass spectrometry (ICP-MS) and inductively coupled plasma-atomic emission spectrometry (ICP-AES) for 40 elements for which we calculated bulk partition coefficients (D = Csolid/Cfluid). Below the solidus, Rb, Sr, Ba, and Pb showed the greatest mobility (D ~ 0.5-1.0), while at the solidus, Th and Be became notably partitioned into the melt (D values changing from >2.0 to <1.0). K and Rb D values fall below 1.0 when the micas breakdown. Only at the solidus do Th and Rb attain similar partition coefficients, a condition required by arc data. Taken together, the experimental results indicate that critical elements (Th and Be) require sediment melting to be efficiently transferred to the arc. This conclusion is at odds with most thermal models for subduction zones, which predict slab temperatures more than 100°C lower than sediment solidi. Thus the condition of sediment melting (with oceanic crust dehydration) may provide new constraints on the next generation of thermal/geodynamical models of subduction zones.
Dehydration and melting experiments constrain the fate of subducted sediments
NASA Astrophysics Data System (ADS)
Johnson, Marie C.; Plank, Terry
2000-12-01
Geochemical tracers demonstrate that elements are cycled from subducted sediments into the arc melting regime at subduction zones, although the transfer mechanism is poorly understood. Are key elements (Th, Be, Rb) lost during sediment dehydration or is sediment melting required? To investigate this question, we conducted phase equilibria and trace element partitioning experiments on a pelagic red clay for conditions appropriate to the slab beneath arc volcanoes (2-4 GPa, 600°-1000°C). Using both piston cylinders and multianvils, we determined the solidus, phase stabilities, and major element compositions of coexisting phases. The solidus (H2O + Cl fluid-saturated) was located at 775 ± 25°C at 2 GPa, 810 ± 15°C at 3 GPa, and 1025 ± 25°C at 4 GPa with noevidence for complete miscibility between melt and fluid. This sediment composition produces a profusion of phases both above and below the solidus: garnet, jadeitic pyroxene, alkali-rich amphibole, phengite, biotite, magnetite, coesite, kyanite, apatite, zircon, Cl-rich fluids, and peraluminous to peralkaline granitic melts. At 2 GPa the phengite dehydration solidus is at 800°-825°C, while biotite breaks down between 850° and 900°C. To explore trace element partitioning across the solidus at 2 GPa, we used diamonds to trap fluids and melts. Both the bulk sediment residues and diamond traps were analyzed postexperiment by inductively coupled plasma-mass spectrometry (ICP-MS) and inductively coupled plasma-atomic emission spectrometry (ICP-AES) for 40 elements for which we calculated bulk partition coefficients (D = Csolid/Cfluid). Below the solidus, Rb, Sr, Ba, and Pb showed the greatest mobility (D ˜ 0.5-1.0), while at the solidus, Th and Be became notably partitioned into the melt (D values changing from >2.0 to <1.0). K and Rb D values fall below 1.0 when the micas breakdown. Only at the solidus do Th and Rb attain similar partition coefficients, a condition required by arc data. Taken together, the experimental results indicate that critical elements (Th and Be) require sediment melting to be efficiently transferred to the arc. This conclusion is at odds with most thermal models for subduction zones, which predict slab temperatures more than 100°C lower than sediment solidi. Thus the condition of sediment melting (with oceanic crust dehydration) may provide new constraints on the next generation of thermal/geodynamical models of subduction zones.
Geology of ultra-high-pressure rocks from the Dabie Shan, Eastern China
NASA Astrophysics Data System (ADS)
Schmid, Robert
2001-02-01
A multidisciplinary study has been carried out to contribute to the understanding of the geologic evolution of the largest known occurrence of ultra-high-pressure (UHP) rocks on Earth, the Dabie Shan of eastern China. Geophysical data, collected along a ca. 20 km E-W trending seismic line in the eastern Dabie Shan, indicate that the crust comprises three layers. The upper crust has a homogeneously low reflectivity and exhibits roughly subhorizontal reflectors down to ca. 15 km. It is therefore interpreted to portray a crustal UHP slab thrust over non-UHP crust. An aprubt change in intensity and geometry of observed reflectors marks the boundary of a mid- to lower crustal zone which is present down to ca. 33 km. This crustal zone likely represents cratonal Yangtze crust that was unaffected by the Triassic UHP event and which has acted as the footwall during exhumation of the crustal wedge. Strong and continuous reflectors occurring at ca. 33-40 km depth most likely trace the Moho at the base of the crust. Any trace of a crustal root, that may have formed in response to collision tectonics, is therefore not preserved. A shollow tomographic velocity modell based on inversion of the first arrivals is constructed additionally. This model clearly images the distinct lithologies on both sides of the Tan Lu fault. Sediments to the east exhibit velocities of about 3.4 - 5.0 km* s^-1, whereas the gneisses have 5.2 - 6.0 km*s^-1. Geometry of velocity isolines may trace the structures present in the rocks. Thus the sediments dip shallowly towards the fault, whereas isoclinal folds are imaged to occur in the gneisses. Field data from the UHP unit of the Dabie Shan enables definition of basement-cover sequences that represent sections of the former passive margin of the Yangtze craton. One of the cover sequences, the Changpu unit, still displays a stratigraphic contact with basement gneisses, while the other, the Ganghe unit, includes no relative basement exposure. The latter unit is in tectonic contact with the basement of the former unit via a greenschist-facies blastomylonite. The Changpu unit is chiefly constituted by calc-arenitic metasediments intercalated with meta-basalts, whereas the Ganghe unit contains arenitic-volcanoclastic metasediments that are likewise associated with meta-basalts. The basement comprises a variety of felsic gneisses, ranging from preserved eclogitic- to greenschist-facies paragenesis, and locally contains mafic-ultramafic meta-plutons in addition to minor basaltic rocks. Metabasites of all lithologies are eclogite-facies or are retrogressed equivalents, which, with the exception of those from the Ganghe unit, bear coesite and thus testify to an UHP metamorphic overprint. Mineral chemistry of the analysed samples reveal large compositional variations among the main minerals, i.e. garnet and omphacite, indicating either distinct protoliths or different degrees of interaction with their host-rocks. Contents of ferric iron in low Fetot omphacites are determined by wet chemical titration and found to be rather high, i.e. 30-40 %. However, a even more conservative estimate of 50% is applied in the corresponding calculations, in order to be comparable with previous studies. Textural constraints and compositional zonation pattern are compatible with equilibrium conditions during peak metamorphism followed by a retrogressive overprint. P-T data are calculated with special focus on the application of the garnet-omphacite-phengite barometer, combined with Fe-Mg exchange thermometers. Maximum pressures range from 42-48 kbar (for the Changpu unit) to ~37 kbar (for the Ganghe unit and basement rocks). Temperatures during the eclogite metamorphism reached ca. 750 °C. Although the sample suite reveals variable peak-pressures, temperatures are in reasonable agreement. Pressure differences are interpreted to be due to strongly Ca-dominated garnet (up to 50 mol % grossular in the Changpu unit) and modification of peak-compositions during retrogressive metamorphism. The integrated geological data presented in this thesis allow it to be concluded that, i) basement and cover rocks are present in the Dabie Shan and both experienced UHP conditions ii) the Dabie Shan is the metamorphic equivalent of the former passive margin of the Yangtze craton iii) felsic gneisses undergoing UHP metamorphism are affected by volume changes due to phase transitions (qtz coe), which directly influence the tectono-metamorphic processes iv) initial differences in temperature may account for the general lack of lower crustal rocks in UHP-facies Um das Verständnis der geologischen Entwicklung des größten bekannten Vorkommens von ultra-hochdruck (UHP) Gesteinen auf der Erde, des Dabie Shan im östlichen China, zu erhöhen, wurde eine multidisziplinäre Studie durchgeführt. Geophysikalische Daten wurden entlang einer ca. 20 km langen seismischen Linie im östlichen Dabie Shan gesammelt. Diese reflektionsseismischen Daten zeigen, dass die Kruste aus drei Lagen besteht. Die Oberkruste besitzt eine durchgehend niedrige Reflektivität und meist subhorizontale Reflektoren bis in eine Tiefe von ca. 15 km. Aufgrund dieser Charakteristika wird diese Zone als UHP-bezogener krustaler Keil interpretiert, der auf nicht UHP Kruste überschoben wurde. Ein abrupter Wechsel in der Geometrie aber auch Intensität der Reflektoren markiert die Grenze zu einer mittel- bis unterkrustalen Zone, die sich bis ca. 33 km Tiefe erstreckt. Diese Zone repräsentiert wahrscheinlich kratonale Yangtze Kruste, die von der triassischen UHP-Orogenese nicht erfasst wurde, aber während der Exhumierung das Liegende relativ zum UHP Keil war. Starke und kontinuierliche Reflektoren im Tiefenintervall von 33-40 km bilden höchstwahrscheinlich die Moho an der Basis der Kruste ab. Relikte einer Krustenwurzel, die sich wahrscheinlich während der Kollisionstektonik gebildet hatte, sind nicht sichtbar. Ein flaches tomographisches Geschwindigkeitsmodell, das auf der Inversion der Ersteinsätze gründet, konnte zusätzlich erstellt werden. Dieses Modell bildet deutlich die unterschiedlichen Lithologien auf beiden Seiten der Tan Lu Störung ab. Sedimente östlich der Störung zeigen Geschwindigkeiten von 3.4 - 5.0 km* s^-1, wohingegen die Gneise im Westen 5.2 - 6.0 km*s^-1 aufweisen. Die Geometrie der Geschwindigkeits-Isolinien kann als Ausdruck der Strukturen der Gesteine angenommen werden. Somit zeigen die Sedimente ein nordwestliches Einfallen zur Störung hin, wohingegen isoklinale Falten in den Gneisen abgebildet werden. Geländedaten aus der UHP Einheit des Dabie Shan ermöglichen die Definition von Grundgebirgs- und Deckeinheiten, die Teile des ehemaligen passiven Kontinentalrandes des Yangtze Kratons repräsentieren. Eine der Deckeinheiten, die Changpu Einheit, besitzt nach wie vor einen stratigraphischen Kontakt zu den Grundgebirgs-Gneisen. Der anderen Einheit hingegen, der Ganghe Einheit, fehlt ein entsprechendes Grundgebirge. Diese Einheit steht vielmehr über einen Blasto-Mylonit in tektonischem Kontakt zum Grundgebirge der vorherigen. Die Changpu Einheit baut sich aus kalk-arenitischen Metasedimenten auf, die mit Metabasalten assoziiert sind. Die Ganghe Einheit wird von arenitisch-vulkanoklastischen Metasedimenten, die ebenfalls mit metabasaltischen Gesteinen vergesellschaftet sind, dominiert. Das Grundgebirge baut sich aus diversen felsischen Gneisen auf, die von reliktisch eklogitfaziell bis grünschieferfaziell ausgeprägt sind, und in denen, zusätzlich zu Metabasalten, sporadisch mafisch-ultramafische Meta-Plutone auftreten. Mit Ausnahme der Ganghe Einheit, führen die Metabasite Coesit und belegen somit das UHP Ereignis. Die Mineralchemie der analysierten Proben dokumentiert deutliche Variationen in der Zusammensetzung der Hauptminerale, Granat und Omphazit, was entweder unterschiedliche Protolithe oder unterschiedliche Grade von Stoffaustausch mit den Wirtsgesteinen reflektiert. Gehalte von dreiwertigem Eisen in Omphaziten mit geringen Gesamteisengehalten, wurden mittels Titration bestimmt, wobei sich Werte von 30-40 % ergaben. Dennoch wurde ein noch konservativerer Wert von 50% dreiwertigem Eisen in den entsprechenden Berechnungen angenommen, hauptsächlich, um mit anderen Arbeiten vergleichbar zu sein. Texturen und chemische Zonierungen in den Mineralen sind kompatibel mit Gleichgewichtsbedingungen während dem Höhepunkt der Metamorphose, der retrograd überprägt wird. P-T Daten wurden mit deutlicher Betonung auf das Granat-Omphazit-Phengit Barometer, das mit Fe-Mg Austausch-Thermometern kombiniert wurde, berechnet. Höchstdrucke reichen von 42-48 kbar (für die Changpu Einheit) bis ca. 37 kbar (für das Grundgebirge und die Ganghe Einheit). Während der eklogitfaziellen Metamorphose wurden Temperaturen von ca. 750 °C erreicht. Obwohl die maximalen Drucke deutlich schwanken, sind die Temperaturbestimmungen in guter Übereinstimmung. Die Druckschwankungen können zum einen durch deutlich Ca-dominierte Granate (bis zu 50 mol% Grossular in der Changpu Einheit) und/oder zum anderen durch Modifikationen der Mineralzusammensetzungen während der retrograden Metamorphose erklärt werden. Die präsentierten integrativen geologischen Daten ermöglichen die folgenden Schlussfolgerungen i) Grundgebirgs- und Deckeinheiten treten im Dabie Shan auf und wurden beide UHP metamorph überprägt ii) Der Dabie Shan ist das metamorphe Äquivalent des früheren passiven Kontinentalrandes des Yangtze Kratons iii) felsische Gneise, die eine UHP Metamorphose durchlaufen, sind von Volumenver-änderungen betroffen, die durch großräumige Phasenumwandlungen (Quarz Coesit) hervorgerufen werden, was direkt die tektono-metamorphen Prozesse beeinflusst iv) Initiale Unterschiede in der Temperatur sind möglicherweise dafür verantwortlich, dass generell Unterkrustengesteine in UHP Fazies fehlen
Minor elements, HREE and d18O distribution in UHP garnets from the Dora-Maira massif (western Alps)
NASA Astrophysics Data System (ADS)
Brunet, F.; Chazot, G.; Vielzeuf, D.; Chopin, C.
2003-04-01
The spatial distribution of minor elements, HREE and δ18O in garnet can be used as a probe of the availability and mobility of those elements and isotopes at the time of crystal growth, provided that the initial record was not significantly modified by intracrystalline diffusion and that growth took place under nearly constant pressure and temperature conditions. Garnets from three different Dora-Maira rock-types have been studied, (1) nearly pure pyrope (GT1) from the magnesian coesite-bearing quartzites, (2) almandine/pyrope dominant garnets (GT2) from jadeite-quartzite veins which crosscut the Mg-quartzite body, (3) almandine/grossular dominant garnets (GT3) from the country-rock gneiss, sampled in the vicinity of the quartzites. In GT1, minor elements are mainly Fe, Na and P. Na and P are incorporated according to a Na^+ + P5+ = Me2+ + Si4+ substitution with P_2O_5 contents up to 2000 to 2500 ppm. HREE concentrations obtained by LA-ICP-MS, vary by 2 orders of magnitude from core to rim. The δ18O ratio (Cameca 1270, Nancy), around 5 ppm (SMOW), is constant within error throughout the analysed crystals. In GT2, the situation is different since HREE concentrations appear remarkably constant within a given crystal and from one crystal to the other. In contrast with GT1, Na in GT2 is partly charge-balanced by yttrium incorporation. The δ18O ratio in GT2 of around 7 ppm is close to that encountered in GT3 (gneiss) between 7 and 8 ppm. In GT3, phosphorus content is close to detection limit (P_2O_5 below 300 ppm). HREE concentrations are highly variable from one crystal to the other and unfortunately, the size of garnet crystals does not allow profiling. Although δ18O ratio in garnet is imposed by the bulk-rock isotopic composition, HREE distribution is dominated by element availability through the fluid composition and/or absence/presence of accessory phases. The decrease in HREE and P concentration from GT1 cores to rims suggest that these elements are preferentially incorporated into garnet. Garnet growth leads to progressive depletion of these elements in the matrix. There is no significant influx of HREE during UHP garnet growth. The homogeneity of the δ18O ratio within garnet crystals is also an indication of UHP growth in a close metamorphic system. Jadeite-quartzite veins have geochemical characteristics close to that of the country-rock gneiss from which they could originate. They would then represent an evidence of Mg-quartzite and country gneiss interaction at UHP.
Effect of water on olivine single crystal plasticity, deformed under upper mantle condition
NASA Astrophysics Data System (ADS)
Girard, J.; Chen, J.; Raterron, P. C.; Holyoke, C. W.
2011-12-01
The earth upper mantle, mainly composed of olivine, is seismically anisotropic. Seismic anisotropy attenuation has been observed at 200km depth. Karato et al. (1992) attributed this attenuation to a transition between two deformation mechanisms, from dislocation creep above 200km to diffusion creep bellow 200km. This transition occurs because of hydroxyl concentration. Mainprice et al.(2005) predicted a change in LPO induced by a change of slip system, from [100] slip to [001] slip, though theoritical modeling. According to his study, pressure is the parameter inducing the slip system transition, which is responsible for the seismic anisotropy attenuation. Raterron et al. (2007) performed single crystal deformation experiment under anhydrous conditions and observe that slip system transition occurring around 8 GPa. However this pressure would correspond to 300km depth which doesn't match the seismic anisotropy attenuation depth, observed by seismologist. In this study, experiments have been performed to quantify the effects of water on olivine single crystals deformed using Deformation DIA press and synchrotron beam. Deformation was carried out in uniaxial compression along the so-called [110]c and [011]c crystallographic direction in order to activate [100](010) and [001](010) dislocation slip system respectively, at P ranging from 4 to 8GPa and T=1200°C. Both single crystals were loaded in the cell to directly compare their deformation in same condition of stress temperature and pressure. We used a sleeve (talc = enstatite + coesite + H2O) about the annulus of the single crystals as source of water in the assembly. Stress and specimen strain rates were calculated by in-situ X-ray diffraction and time resolved imaging, respectively. By direct comparison of single crystals strain rates, we observed that [110]c deform faster than [011]c bellow 5GPa. However above 6GPa [011]c deform faster. This revealed that [100](010) is the dominant slip system bellow 5GPa, and [001](010) becomes dominant above 6GPa. Thus, we observe a slip system switch over at about 5-6GPa in wet condition. This slip system switch over will result in change of lattice preferred orientation in olivine, from [100] slip to [001] slip, and therefore reduce seismic anisotropy attenuation down to 1.9% (Mainprice et al.,2005). According to our results, the slip system transition is induced by pressure, and water influences the pressure where the switch over occurs. These results not only can explain the depth where the seismic anisotropy attenuation (i.e. 200 km, corresponding to 6GPa) but also can help to understand the regional variation of the depth, as local hydroxyl contents in the mantle may varies significantly. TEM investigation and water content measurement of recovered specimens from the deformation experiments will also be discussed.
NASA Astrophysics Data System (ADS)
Sobolev, N. V.; Palyanov, Y. N.; Shatsky, V. S.; Sokol, A. G.; Tomilenko, A. A.
2003-12-01
Garnet is a key mineral coexisting with diamond both in kimberlite (as xenocrysts, in diamondiferous garnet peridotites and eclogites, as inclusions in diamond) and in UHP metamorphic rocks of Kokchetav massif (diamondiferous gneisses, garnet-pyroxene rocks, dolomitic marbles and diamond facies eclogites). In UHPM rocks garnets are of particular importance as inclusions in zircons protected from retrograde metamorphism. Diamond formation conditions in eclogitic (E-type) upper mantle environment are estimated based upon Grt-Cpx thermometry and coesite barometry (e.g. Sobolev et al., PNAS, 2000, 97:11875) at P=5.5-6.0 GPa and T=1000-1300° C. These data are supported by diamond synthesis in carbonate-silicate fluid (e.g. Palyanov et al., Nature, 1999, 400: 417). E-type garnet may dissolve up to 0.3 wt.% Na2O (Sobolev, Lavrentyev, Contr. Min. Petr., 1971, 31:1) depending on pressure and Na2O contents in coexisting pyroxene and melts (fluids). Majorite component (pyroxene solid solution) was reported in rare garnets from diamonds (e.g. Moore, Gurney, Nature, 1985, 318:553) and UHP conditions were experimentally confirmed for such garnets (Irifune, Phys. Eart. Pl. Int., 1987, 45:324; Gasparik, Phys. Chem. Min., 2002, 29:170; Luth, Am. Miner., 1997, 82:1198). Garnets from Kokchetav diamondiferous metamorphic rocks demonstrate considerably lower Na2O solubility (up to 0.2 wt.% in rare samples) and absence of majorite component. However, coexisting pyroxenes may contain up to 50 mol.% jadeite. Several UHP experiments performed with Kokchetav eclogites and dolomitic marbles using a split-sphere apparatus resulted in detection of up to 0.3-0.4 wt.% Na2O in newly formed eclogitic garnets at P=5.7 and 7.0 GPa, T=1400 and 1700° C respectively. Majorite component was also determined in newly formed garnets reaching about 5% with Si (pfu)=3.05-3.06. Similar garnets without Na2O were also obtained in UHP experiments with diamondiferous dolomitic marbles (e.g. Palyanov et al., Dokl. Earth. Sci., 2001, 380:671). Based on the difference in Na2O and majorite contents in natural Kokchetav garnets, and those coexisting with diamonds in kimberlite and obtained in UHP experiments, we conclude that the peak of metamorphism at Kokchetav massif occurred at P about 4.5-5.0 GPa and T=900-1000° C (Sobolev, Shatsky, Nature, 1990, 343:742; Shatsky et al., Contr. Min. Petr., 1999, 137:185; Sobolev et al., Dokl. Earth. Sci., 2001, 380:237) but not exceeding 6.0 GPa (e.g. Ogasawara et al., Island Arc, 2000, 9:400).
Developments in Laser-Ablation Split-Stream Petrochronology
NASA Astrophysics Data System (ADS)
Kylander-Clark, Andrew R.
2017-04-01
One of the biggest challenges in assessing the timing and rates of petrogenesis and deformation is having the ability to match the age of a dated mineral to the conditions at which that mineral grew. This is especially challenging for high-temperature chonometers that can grow and remain stable over a wide range of pressures and temperatures. The development of the laser-ablation split-stream method has afforded the ability to rapidly aquire chemical and chronologic data that are directly linked; as such, timing and rates of processes are better constrained than before. Several examples are given within: 1) Zircon and monazite from a single, coesite-bearing sample from the Western Gneiss Region in western Norway record the entire 30+ Myr history of metamorphism during Caledonian orogenesis, from intial burial, through ultrahigh-pressure (UHP) conditions, and back to crustal levels. Early monazite ( 425 Ma) contains low concentrations of Sr and HREE, consistent with plagioclase and garnet stability during prograde metamorphism. 420-400 Ma ages from monazite (high Sr, increased Eu/Eu*, low HREE) and zircon (increased Eu/Eu*, low HREE) indicate the timing of HP conditions, and monazite with low Sr and high HREE indicates the breakdown of omphacite and garnet at 390 Ma. 2) Titanite is becoming more widely used as chronometer, primarly because laser ablation has made analysis more feasible. Nevertheless, dates produced from titanite can be difficult to interpret because titanite may alter more easily than zircon and monazite. LASS analyses of titanite, combined with X-ray maps and backscattered electron images provide insight into processes involved in growth, recrystallization and dissolution/reprecipitation, and allow us to better interpret ages and the geologic process that they represent. This study presents recrystallized titanite from metamorphic terranes as well as ocillatory-zoned titanite from igneous rocks, and suggests some possible processes that explain the TE/age trends. 3) Detrital zircons have long been used to investigate the location and geology of landforms in the past. By adding chemical information to the age data, a clearer history can be produced. Recent LASS data from Mesozoic sedimentary rocks indicate changes in chemistry of the Sierra Nevada-Peninsular Ranges batholith, as well and the exposure and erosion of distinct units (e.g., ophiolites) over discrete time periods. 4) Isotopic data retrieved in combination with age data across an orogeny or batholith can aid in the understanding of the areal and temporal evolution of both deformation and source rocks over time. This can be done with a number of petrochronometers: Hf in zircon, Nd in titanite and monazite, This study presents examples that show how significant advances can be made in understanding lithosphere evolution using this quick and efficient analytical technique.
Single inclusion piezobarometry confirms high-temperature decompression path for Variscan granulites
NASA Astrophysics Data System (ADS)
Angel, Ross; Alvaro, Matteo; Mazzucchelli, Mattia; Nimis, Paolo; Nestola, Fabrizio
2016-04-01
The identification and chemistry of inclusions trapped in host minerals during growth of the host phase have long been used to infer P-T points on metamorphic paths. The determination of the remnant pressure on the inclusion, e.g., using data from X-ray diffractometry, birefringence analysis or Raman spectroscopy, provides an alternative method of barometry using elasticity theory. A remnant pressure in an inclusion is developed because the inclusion and the host have different thermal expansion and compressibilities, and the inclusion does not expand in response to P and T as would a free crystal. Instead it is restricted to expand only as much as the host mineral, and this constriction in volume can result in inclusions exhibiting over-pressures when the host is studied at room conditions. This concept has been known for a long time, but satisfactory quantitative modelling of inclusion-host systems based on non-linear elasticity theory and precise thermal-pressure euqations of state has only recently come available (Angel et al., 2014, 2015), even though it is still restricted to elastically isotropic minerals. No mineral is elastically isotropic, but garnets and diamond are almost so. Calculations show that diamonds trapped as inclusions in host silicates at P and T within the stability field of diamond should exhibit zero pressure when the samples are recovered to room conditions. However, some diamond inclusions in garnets in granulites are reported to exhibit significant residual overpressures (e.g., Kotková et al., 2011). This indicates that the inclusion was elastically re-equilibrated (e.g., by plastic flow in the garnet host) at high temperatures and lower pressures in the stability field of graphite, consistent also with the observed partial inversion of diamond to graphite. In this case, the elastic analysis of the diamond-in-garnet inclusions provides qualitative independent evidence that the Variscan granulites underwent pressure reduction at high temperatures. The extension of single inclusion piezobarometry to elastically anisotropic minerals will allow quantitative analysis of diamonds trapped in other minerals such as kyanite. This work was supported by ERC starting grant 307322 to Fabrizio Nestola and by the MIUR-SIR grant "MILE DEEp" (RBSI140351) to M. Alvaro. Angel R.J., Mazzucchelli M.L., Alvaro M., Nimis P. & Nestola F. (2014) Geobarometry from host-inclusion systems: the role of elastic relaxation. Am. Mineral., 99, 2146-2149. Angel R.J., Nimis P., Mazzucchelli M.L., Alvaro M. & Nestola F. (2015) How large are departures from lithostatic pressure? Constraints from host-inclusion elasticity. J. Metamorphic Geol., 33, 801-813. Kotková J, O'Brien P.J & Ziemann M.A. (2011)Diamond and coesite discovered in Saxony-type granulite: Solution to the Variscan garnet peridotite enigma. Geology, 39, 667-670.
Belkin, H.E.; Horton, J. Wright
2009-01-01
Optical and electron-beam petrography of melt-rich suevite and melt-rock clasts from selected samples from the Eyreville B core, Chesapeake Bay impact structure, reveal a variety of silicate glasses and coexisting sulfur-rich melts, now quenched to various sulfi de minerals (??iron). The glasses show a wide variety of textures, fl ow banding, compositions, devitrifi cation, and hydration states. Electron-microprobe analyses yield a compositional range of glasses from high SiO2 (>90 wt%) through a range of lower SiO2 (55-75 wt%) with no relationship to depth of sample. Some samples show spherical globules of different composition with sharp menisci, suggesting immiscibility at the time of quenching. Isotropic globules of higher interfacial tension glass (64 wt% SiO2) are in sharp contact with lower-surface-tension, high-silica glass (95 wt% SiO2). Immiscible glass-pair composition relationships show that the immiscibility is not stable and probably represents incomplete mixing. Devitrifi cation varies and some low-silica, high-iron glasses appear to have formed Fe-rich smectite; other glass compositions have formed rapid quench textures of corundum, orthopyroxene, clinopyroxene, magnetite, K-feldspar, plagioclase, chrome-spinel, and hercynite. Hydration (H2O by difference) varies from ~10 wt% to essentially anhydrous; high-SiO2 glasses tend to contain less H2O. Petrographic relationships show decomposition of pyrite and melting of pyrrhotite through the transformation series; pyrite? pyrrhotite? troilite??? iron. Spheres (~1 to ~50 ??m) of quenched immiscible sulfi de melt in silicate glass show a range of compositions and include phases such as pentlandite, chalcopyrite, Ni-As, monosulfi de solid solution, troilite, and rare Ni-Fe. Other sulfi de spheres contain small blebs of pure iron and exhibit a continuum with increasing iron content to spheres that consist of pure iron with small, remnant blebs of Fe-sulfi de. The Ni-rich sulfi de phases can be explained by melting and/or concentrating targetderived Ni without requiring an asteroid impactor source component. The presence of locally unaltered glasses in these rocks suggests that in some rock volumes, isolation from postimpact hydrothermal systems was suffi cient for glass preservation. Pressure and temperature indicators suggest that, on a thin-section scale, the suevites record rapid mixing and accumulation of particles that sustained widely different peak temperatures, from clasts that never exceeded 300 ?? 50 ??C, to the bulk of the glasses where melted sulfi de and unmelted monazite suggest temperatures of 1500 ?? 200 ??C. The presence of coesite in some glass-bearing samples suggests that pressures exceeded ~3 GPa. ?? 2009 Geological Society of America.
Metamorphism, Plate Tectonics, and the Supercontinent Cycle
NASA Astrophysics Data System (ADS)
Brown, Michael
Granulite facies ultrahigh temperature metamorphism (G-UHTM) is documented in the rock record predominantly from Neoarchean to Cambrian; G-UHTM facies series rocks may be inferred at depth in younger, particularly Cenozoic orogenic systems. The first occurrence of G-UHTM in the rock record signifies a change in geodynamics that generated transient sites of very high heat flow. Many G-UHTM belts may have developed in settings analogous to modern continental backarcs. On a warmer Earth, the cyclic formation of supercontinents and their breakup, particularly by extroversion, which involved destruction of ocean basins floored by thinner lithosphere, may have generated hotter continental backarcs than those associated with the modern Pacific rim. Medium-temperature eclogite, high-pressure granulite metamorphism (E-HPGM), is also first recognized in the Neoarchean rock record and occurs at intervals throughout the Proterozoic and Paleozoic rock record. E-HPGM belts are complementary to G-UHTM belts and are generally inferred to record subduction-to-collision orogenesis. Blueschists become evident in the Neoproterozoic rock record; they record the low thermal gradients associated with modern subduction. Lawsonite blueschists and eclogites (high-pressure metamorphism, HPM) and ultrahigh pressure metamorphism (UHPM) characterized by coesite (±lawsonite) or diamond are predominantly Phanerozoic phenomena. HPM-UHPM registers the low thermal gradients and deep subduction of continental crust during the early stage of the collision process in Phanerozoic subduction-to-collision orogens. Although perhaps counterintuitive, many HPM-UHPM belts appear to have developed by closure of small ocean basins in the process of accretion of a continental terrane during a period of supercontinent introversion (Wilson cycle ocean basin opening and closing). A duality of metamorphic belts—reflecting a duality of thermal regimes—appears in the record only since the Neoarchean Era. A duality of thermal regimes is the hallmark of modern plate tectonics and the duality of metamorphic belts is the characteristic imprint of plate tectonics in the rock record. The occurrence of both G-UHTM and E-HPGM belts since the Neoarchean manifests the onset of a 'Proterozoic plate tectonics regime', although the style of tectonics likely involved differences. The 'Proterozoic plate tectonics regime' evolved during a Neoproterozoic transition to the 'modern plate tectonics regime' characterized by colder subduction and subduction of continental crust deep into the mantle and its (partial) return from depths of up to 300 km, as chronicled by the appearance of HPM-UHPM in the rock record. The age distribution of metamorphic belts that record extreme conditions of metamorphism is not uniform, and metamorphism occurs in periods that correspond to amalgamation of continental lithosphere into supercratons (e.g. Superia/Sclavia) or supercontinents (e.g. Nuna (Columbia), Rodinia, Gondwana, and Pangea).
NASA Astrophysics Data System (ADS)
Grevel, K. D.
2008-12-01
In order to enable reliable calculations of phase relations among high-pressure phases the Berman [1] data set was augmented by data for the high-pressure phases stishovite (stv), topaz-OH (toz-OH), phase pi (pi), Mg-staurolite (Mg-st), Mg-sursassite (Mg-sur), and Mg-chloritoid (Mg-cld) using a similar optimization technique as described by Berman et al. [2]. The data of several other phases of the system CaO-MgO- Al2O3-SiO2-H2O obtained in the Berman data base were slightly refined to keep the consistency to the reversal brackets and the originally measured data: andalusite (and), clinochlore (chl), coesite (cs), diaspore (dsp), kaolinite (kln), kyanite (ky), lawsonite (lws), pyrophyllite (prl), sillimanite (sil), zoisite (zo). CP-data were kept constant [1] or estimated [3]. phase; ΔfH0298 (kJ mol-1); S0298 (J K-1 mol-1); V0298 (J K-1 mol-1); v1×105 (bar-1); v2×1012 (bar-2); v3×105 (K-1); v4×108 (K-2) and; -2589.857; 91.47; 5.146; -0.0653; 0.000; 2.291; 0.170 chl; -8903.532; 437.92; 21.000; -0.1328; 3.837; 2.142; 0.962 Mg-cld; -3551.657; 142.20; 6.874; -0.0692; 0.000; 2.544; 0.000 cs; -907.510; 39.63; 2.064; -0.0998; 1.823; 0.620; 0.960 dsp; -999.115; 35.22; 1.776; -0.0719; 0.629; 3.245; 0.684 kln; -4119.400; 204.18; 9.952; -0.1200; 0.000; 3.200; 0.000 ky; -2593.767; 82.71; 4.408; -0.0593; 1.021; 1.730; 0.787 lws; -4866.665; 228.04; 10.155; -0.0825; 0.000; 3.339; 0.000 Mg-sur; -13907.329; 608.39; 26.888; -0.0826; 0.923; 3.187; 0.087 pi; -9586.742; 403.23; 18.559; -0.0678; 0.000; 2.254; 0.000 prl; -5640.501; 239.43; 12.782; -0.1800; 0.000; 2.621; 0.000 sil; -2586.169; 95.40; 4.984; -0.0601; 1.341; 1.138; 0.605 Mg-st; -24998.289; 944.53; 44.260; -0.0579; 0.000; 2.017; 0.000 stv; -870.861; 25.59; 1.401; -0.0318; 0.000; 1.849; 0.000 toz-OH; -2885.939; 117.40; 5.352; -0.0630; 0.000; 1.938; 0.000 zo; -6889.494; 297.20; 13.565; -0.0695; 0.000; 2.752; 0.000 References [1] R.G. Berman, J. Petrol., 1988, 29, 445 [2] R.G. Berman et al., J. Petrol., 1986, 27, 1331 [3] R.G. Berman, T.H. Brown, Con. Min. Pet., 1985, 89, 168
NASA Astrophysics Data System (ADS)
Cheng, N.; Jenkins, D. M.
2017-12-01
Pyrope (Mg3Al2Si3O12) is the dominant component in garnets from type A eclogites. Determining the lower-pressure-temperature (P-T) stability of pyrope in the presence of quartz helps put constraints on the stability of quartz-bearing eclogites and therefore the depths to which crustal rocks in high pressure/ultra-high pressure (HP/UHP) terranes can be transferred. It also defines the lower-pressure stability of the nearly pure pyrope-bearing quartzites of the Dora Maira massif of the Western Alps (Chopin, 1984, Contrib. Min. Pet.). Aside from the approximate boundary proposed by Hensen & Essene (1971, Contrib. Min. Pet.), there has been no detailed study of the lower P-T stability of pyrope + quartz. A reversed determination of the reaction 3 enstatite + 2 kyanite = 2 pyrope + 2 quartz has been done in the system MgO-Al2O3-SiO2 over the P-T range of 900-1100 °C and 1.6-2.5 GPa for durations of 24 hours. Double capsules, one using pure enstatite and the other Al-rich (10 wt% Al2O3) enstatite in the starting mixtures, were used to obtain reversals on the Al content in the orthopyroxene (Opx). Experiments were done using a ½-inch diameter piston-cylinder press and NaCl-pyrex-MgO pressure media. Run products were analyzed using powder XRD and electron microprobe. Reaction direction was readily determined from peak height changes on XRD patterns. The reaction has been bracketed at 1.65 GPa at 1100 °C with > 12 wt% Al2O3 in Opx; 2.05 GPa at 1000 °C with 10 wt% Al2O3 in Opx; and 2.4 GPa at 930 °C with 5 wt% Al2O3 in Opx. The reaction boundary is slightly curved to higher P with increasing T caused by increasing Al in Opx. The boundary observed in this study is about 100 °C or 0.4 GPa higher than previously proposed by Hensen & Essene (1971) and 70-170 °C or 0.6-0.7 GPa higher than the boundary calculated in this system using THERMOCALC ds6.22 (Holland & Powell, 2011, J. Meta. Geol.) and about 1-4 wt% higher Al2O3 contents in Opx. Higher pressure runs in the field of coesite are being done using a multi-anvil press to extend these results to the lower T range reported for many UHP terranes. Minor extrapolation of the present data to lower T puts the absolute minimum depth for pyrope-quartzites in Dora Maira at 95 km (3.0 GPa) at 800°C; even greater depths are expected for the reaction of pyrope + quartz + H2O to talc-bearing assemblages.
Velocities of Subducted Sediments and Continents
NASA Astrophysics Data System (ADS)
Hacker, B. R.; van Keken, P. E.; Abers, G. A.; Seward, G.
2009-12-01
The growing capability to measure seismic velocities in subduction zones has led to unusual observations. For example, although most minerals have VP/ VS ratios around 1.77, ratios <1.7 and >1.8 have been observed. Here we explore the velocities of subducted sediments and continental crust from trench to sub-arc depths using two methods. (1) Mineralogy was calculated as a function of P & T for a range of subducted sediment compositions using Perple_X, and rock velocities were calculated using the methodology of Hacker & Abers [2004]. Calculated slab-top temperatures have 3 distinct depth intervals with different dP/dT gradients that are determined by how coupling between the slab and mantle wedge is modeled. These three depth intervals show concomitant changes in VP and VS: velocities initially increase with depth, then decrease beyond the modeled decoupling depth where induced flow in the wedge causes rapid heating, and increase again at depth. Subducted limestones, composed chiefly of aragonite, show monotonic increases in VP/ VS from 1.63 to 1.72. Cherts show large jumps in VP/ VS from 1.55-1.65 to 1.75 associated with the quartz-coesite transition. Terrigenous sediments dominated by quartz and mica show similar, but more-subdued, transitions from ~1.67 to 1.78. Pelagic sediments dominated by mica and clinopyroxene show near-monotonic increases in VP/ VS from 1.74 to 1.80. Subducted continental crust that is too dry to transform to high-pressure minerals has a VP/ VS ratio of 1.68-1.70. (2) Velocity anisotropy calculations were made for the same P-T dependent mineralogies using the Christoffel equation and crystal preferred orientations measured via electron-backscatter diffraction for typical constituent phases. The calculated velocity anisotropies range from 5-30%. For quartz-rich rocks, the calculated velocities show a distinct depth dependence because crystal slip systems and CPOs change with temperature. In such rocks, the fast VP direction varies from slab-normal at shallow depths through trench-parallel at moderate depths to down-dip approaching sub-arc depths. Vertically incident waves have VP/ VS of 1.7-1.3 over the same range of depths, waves propagating up dip have VP/ VS of 1.7-1.3, and waves propagating along the slab at constant depth have VP/ VS of 1.7-1.45. These remarkably low VP/ VS ratios are due to the anomalous elastic behavior of quartz. More aluminous lithologies have elevated VP/ VS ratios: 1.85 for slab-normal waves, 1.75 for trench-parallel waves, and 1.65 for down-dip waves. Subducted continental crust that is too dry to transform to high-pressure minerals has relatively ordinary VP/ VS ratio of 1.71-1.75 for vertically incident waves, 1.6-1.7 for waves propagating up dip, and 1.65-1.75 for waves propagating along the slab. Thus, subducted mica-rich sediments can have high VP/ VS ratios, whereas quartzose lithologies generate low VP/ VS ratios.
NASA Astrophysics Data System (ADS)
Butvina, Valentina; Litvin, Yurii
2010-05-01
Peridotites and eclogites, including diamond-bearing ones, are the basic ultra-basic and basic rocks of the upper mantle (Ringwood, 1969, 1975; Sobolev, 1974; Marakushev, 1985; Taylor & Anand, 2004). These rocks are presented in the assemblage of mantle xenolyths in kimberlites, but the basic minerals of peridotite paragenesis, olivine, orthopyroxene, garnet and clinopyroxene as well as of an eclogite paragenesis, garnet and omphacite are wide-spread synthetic inclusions in diamonds. The cases of finding minerals and peridotite and eclogite parageneses in diamond are described. It implies that these parageneses can have a single mantle source. However, the formation of peridotite and eclogite mineral parageneses at differentiation of the primary ultrabasite melt during physico-chemical single process is possible only at overcoming the 'eclogite' thermal barrier (O'Hara, 1968; Litvin, 1991). Eclogite genesis is one of the most difficult and discussional problems of modern petrology. Among investigators there is an opinion about eclogite heterogeneity not only on conditions of formation (crust, mantle), but also by composition of the initial rocks (para-, orthoeclogites) as well as by the way of their formation (magmatic, metamorphic, metasomatic). In literature diamond-bearing eclogite nodules of kimberlite pipes are often considered as metamorphic, which are formed at subduction of the Archean or of the Proterozoic oceanic crust (MacGregor & Manton, 1986; McCandless & Gurney, 1986, 1997 et al.). Only the presence of Na2O in garnet and K2O in clinopyroxene is a criterion of their participation in mantle magmatic processes. Together with the hypotheses considered on eclogite origin there exists a version suggested in papers (Kushiro, 1972; Kushiro & Yoder, 1974), according to which mantle eclogites could be formed due to peridotite substance in the processes of fractional crystallization of ultrabasite magmas. The present paper is devoted to the experimental study of this problem. Physico-chemical transition from peridotite assemblage to the eclogite one can be only ensured by the processes of fractional crystallization of mantle magmatic melts. The primary melting and magmatic evolution of mantle garnet lerzolite (or the Ringwood pyrolite) is controlled by a five-phase peritectics 'p' Ol+Opx+Cpx+Grt+L and four cotectic curves conjugated to it (Litvin, 1991). In melting and evolution of melts of both olivine eclogites and coesite and corundum eclogites the corresponding five-phase eutectics are of a dominant importance. A general ridge for all elementary tetrahedrons (simplexes) is a line of compositions diopside-pyrope (clinopyroxene-garnet) which bimineral eclogite assemblages belong to. The internal section En-Di-Cor of the general tetrahendric diagram (symplex complex) separates olivine-saturated and silica-saturated compositions. 'Eclogite' thermal barrier is 'thermal barrier' on (O'Hara, 1968), on the cotectic line Opx+Cpx+Grt+L, connecting 'peridotite' peritectic and 'eclogite' eutectic points. Meanwhile, at equilibrium (and fractional) crystallization of peridotite system in the peritectic point 'p' orthopyroxene vanishes as a result of the peritectic reaction 'orthopyroxene + melt - clinopyroxene' (Davis, 1963; Litvin, 1991). With further temperature decrease the composition of the remnant melt is controlled by the nonorthopyroxene cotectics Ol+Cpx+Grt+L first, in the limits of the peridotite 'simplex', but then mechanism of fractional crystallization is also realized in the limits of the olivine-eclogite 'simplex' up to the corresponding nonvariant eutectics. The considered cotectics Ol+Cpx+Grt+L is of the greatest interest from the viewpoint of a possible change of compositions of remnant melts from olivine-normative to silica-normative ones. One can assume that under the conditions of fractional melt crystallization along the cotectic curve Ol+Cpx+Grt+L together with olivine jigging accumulation of incorehent elements, including Na, Fe etc. takes place. It leads to a gradual increase of jadeite component content in remnant melts what creates grounds for reactional interaction of jadeite and olivine components with olivine vanishing and garnet formation in accordance with the reaction found in (Litvin et al., 2004). A gradual decrease of olivine component content in remnant melts caused by that fact realizes a 'turn' to the cotectic curve Ol+Cpx+Grt+L in the direction of the boundary section En - Di - Cor and, probably its exit to the line Di-Prp (clinopyroxene-garnet). Further under the conditions of fractional crystallization melt composition point can penetrate into the volumes of coesite-eclogite, kyanite-eclogite and corundum-eclogite 'symplexes'. Thus, an overcoming of 'eclogite' thermal barrier between olivine-normative peridotite-pyroxene and SiO2 - normative eclogite compositions occurs. So, one can speak about the 'destruction' of liquidus peridotite-eclogite thermal barrier in the limits of the peridotite 'simplex' as a result of realization of two reaction mechanisms: (1) vanishing of orthopyroxene as a result of its peritectic reaction with the melt with clinopyroxene formation and (2) olivine vanishing as a result of its reactional interaction of jadeite with garnet formation. If with respect to the first mechanism definite experimental evidence exists (Litvin, 1991; Davis, 1963) then for the second mechanism it is absent. Due to this fact the main purpose of this paper is an experimental study of phase relationships in the model system forsterite-dioside-jadeite at pressure of 7 GPa and foundation of possible physico-chemical correct transitions between peridotite and eclogite parageneses with overcoming liquidus 'eclogite' thermal barrier. To construct a diagram of a ternary system forsterite-diopside-jadeite it is necessary to study its boundary binary sections forsterite-jadeite and fosterite-diopside as well as a number of internal polythermic sections. The section jadeite-diopside at 7 GPa has been studied earlier (Bobrov, Litvin, Kojitani, Akaogi, 2006; 2008) and it is characterized by the unlimited miscibility of jadeite and diopside components in solid and liquid states. The first experimental results obtained at the initial stage of the investigation of this problem can be characterized as follows. For the experimental study polythermic sections of forsterite-(jadeite50diopside50) and forsterite-(jadeite25diopside75) have been chosen. The obtained data testify to the fact that olivine vanishing and garnet formation are realized in both sections. The problem of further investigations is to search minimum concentrations of jadeite in the composition of this system where a total olivine vanishing takes place. Thus, the performed experimental investigations of the model system forsterite-diospside-jadeite at pressure 7 GPa testify to the fact that forsterite (olivine) is a stable phase in the boundary system forsterite-diopside (olivine-clinopyroxene). While introducing rather low contents of jadeite component into the composition of this system the reaction of jadeite component with forsterite takes place in the melt. As a result, garnet appears as liquidus phase.
NASA Astrophysics Data System (ADS)
Poli, S.
2013-12-01
Current knowledge on the solidus temperature for carbonate-bearing rocks suggests that carbonatitic liquids should not form in a subducted oceanic lithosphere, unless anomalous thermal relaxation occurs. For a mildly warm subduction path, COH-bearing basaltic eclogites are expected to loose all H2O component at epidote breakdown, located at approx. 2.8-3.0 GPa. Above this pressure limit, the solidus is that of a carbonated basaltic eclogite which shows a minimum temperature of 1020 °C at 4.0-4.5 GPa (Dasgupta et al. 2004). However, the oceanic crust includes a range of gabbroic rocks, altered on rifts and transforms, with large amounts of An-rich plagioclase. It has been shown that epidote disappearance with pressure depend on the normative anorthite content of the bulk composition considered (Poli et al. 2009); we therefore expect that altered gabbros might display a much wider pressure range where epidote persists, potentially affecting the solidus relationships. Notably, this applies to epidosite rocks formed in hydrothermal environments at oceanic settings, then recovered in high-pressure and ultra-high pressure terrains. New experimental data from 3.7 to 4.6 GPa, 750°C to 1000 °C are intended to unravel the effect of variable bulk and volatile compositions in model eclogites, enriched in the normative anorthite component (An37 and An45). Experiments are performed in piston cylinder and multianvil machines apparatus, using both single and, buffered, double capsule techniques. Garnet, clinopyroxene and coesite form in all syntheses. Lawsonite was found to persist at 3.7 GPa, 750 °C, with both dolomite and magnesite; at 3.8 GPa, 775-800 °C, fluid saturated conditions, epidote coexists with kyanite, dolomite and magnesite. The anhydrous assemblage garnet, omphacite, aragonite, kyanite is found at 4.2 GPa, 850 °C. At 900 °C, fluid-rich conditions, a silicate fluid/melt of granitoid composition, a carbonatitic melt and Na-carbonate are observed. Close to fluid-saturation, 3.8-4.2 GPa, 900 °C, garnet and Na-rich clinopyroxene coexist with a carbonatitic melt and dolomite. The carbonatitic melt is richer in Ca compared to dolomite, consistently with phase relationships in the model system MgCO3-FeCO3-CaCO3. In fluid-undersaturated compositions, fluid-absent melting of epidote + dolomite, enlarged in its pressure stability for An-rich gabbros, is expected to promote the generation of carbonatitic liquids. The subsolidus breakdown of epidote in the presence of carbonates at depths exceeding 120 km provides a major source of COH fluids at subarc depth. In warm subduction zones, the possibility of extracting carbonatitic liquids from a variety of gabbroic rocks and epidosites offers new scenarios on the metasomatic processes in the lithospheric wedge of subduction zones and a new mechanism for recycling carbon. Dasgupta R., Hirschmann M.M., Withers A. (2004) Earth Planet Sci Lett, 227: 73-85 Poli S., Franzolin E., Fumagalli P., Crottini A. (2009) Earth Planet Sci Lett, 278: 350-360
NASA Astrophysics Data System (ADS)
Litvin, Yuriy; Kuzyura, Anastasia
2017-04-01
Ultrabasic peridotites and pyroxenites together with basic eclogites are the upper-mantle in situ rocks among xenoliths in kimberlites. Occasionally their diamond-bearing varieties have revealed within the xenoliths. Therewith the compositions of rock-forming minerals demonstrate features characteristic for primary diamond-included minerals of peridotite and eclogite parageneses (the elevated contents of Cr-component in peridotitic garnets and Na-jadeitic component in eclogitic clinopyroxenes). High-pressure experimental study of melting equilibria on the multicomponent peridotie-pyroxenite system olivine Ol - orthopyroxene Opx - clinopyroxene Cpx - garnet Grt showed that Opx disappeared in the peritectic reaction Opx+L→Cpx (Litvin, 1991). As a result, the invariant peritectic equilibrium Ol+Opx+Cpx+Grt+L of the ultrabasic system was found to transform into the univariant cotectic assemblage Ol+Cpx+Grt+L. Further experimental investigation showed that olivine reacts with jadeitic component (Jd) with formation of garnet at higher 4.5 GPa (Gasparik, Litvin, 1997). Study of melting relations in the multicomponent system Ol - Cpx - Jd permits to discover the peritectic point Ol+Omph+Grt+L (where Omph - omphacitic clinopyroxene) at concentration 3-4 wt.% Jd-component in the system. The reactionary loss of Opx and Ol makes it possible to transform the 4-phase garnet lherzolite ultrabasic association into the bimineral eclogite assemblage. The regime of fractional Ol, Cpx and Grt crystallization must be accompanied by increasing content of jadeitic component in residual melts that causes the complete "garnetization of olivine". In the subsequent evolution, the melts would have to fractionate for basic SiO2-saturated compositions responsible for petrogenesis of eclogite varieties marked with accessory corundum Crn, kyanite Ky and coesite Coe. Both the peritectic mechanisms occur in regime of fractional crystallization. The sequence of the upper-mantle fractional ultrabasic-basic magmatic evolution and petrogenesis may be controlled by the following melting relations: from Ol, Opx, L field to cotectic curve Ol, Opx, Cpx, L, peritectic point Ol, Opx, Cpx, Grt, L (loss of Opx), cotectic curve Ol, (Cpx+Jd), Grt, L, peritectic point Ol, (Cpx→Omph), Grt, L (loss of Ol), divariant field Omph,Grt,L, cotectic curve Ky, Omph, Grt, L, eutectic point Ky,Coe,Omph, Grt,L, subsolidus assemblage Ky,Coe,Omph, Grt. The fractional ultrabasic-basic evolution of the upper-mantle silicate-carbonate-carbon melts-solutions, which are responsible for genesis of diamond-and-inclusions associations and diamond-bearing peridotites and eclogites, follows the similar physico-chemical mechanisms (Litvin et al., 2016). This is illustrated by fractional syngenesis diagram for diamonds and associated minerals which construction is based on evidence from high pressure experiments. References Gasparik T., Litvin Yu.A (1997). Stability of Na2Mg2Si2O7 and melting relations on the forsterite - jadeite join at pressures up to 22 GPa. Eur, J. Mineral. 9(2), 311-326. Litvin Yu.A. (1991). Physico-Chemical Study of Melting of Materials from the Deep Earth. Moscow: Nauka. 312 p. Litvin Yu.A., Spivak A.V., Kuzyura A.V. (2016). Fundamentals of the mantle-carbonatite concept of diamond genesis, Geochemistry Internat. 34(10), 839-857.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Leinenweber, Kurt, E-mail: kurtl@asu.edu; Gullikson, Amber L.; Stoyanov, Emil
2015-09-15
The accuracy and precision of pressure measurements and the pursuit of reliable and readily available pressure scales at simultaneous high temperatures and pressures are still topics in development in high pressure research despite many years of work. In situ pressure scales based on x-ray diffraction are widely used but require x-ray access, which is lacking outside of x-ray beam lines. Other methods such as fixed points require several experiments to bracket a pressure calibration point. In this study, a recoverable high-temperature pressure gauge for pressures ranging from 3 GPa to 10 GPa is presented. The gauge is based on themore » pressure-dependent solubility of an SiO{sub 2} component in the rutile-structured phase of GeO{sub 2} (argutite), and is valid when the argutite solid solution coexists with coesite. The solid solution varies strongly in composition, mainly in pressure but also somewhat in temperature, and the compositional variations are easily detected by x-ray diffraction of the recovered products because of significant changes in the lattice parameters. The solid solution is measured here on two isotherms, one at 1200 °C and the other at 1500 °C, and is developed as a pressure gauge by calibrating it against three fixed points for each temperature and against the lattice parameter of MgO measured in situ at a total of three additional points. A somewhat detailed thermodynamic analysis is then presented that allows the pressure gauge to be used at other temperatures. This provides a way to accurately and reproducibly evaluate the pressure in high pressure experiments and applications in this pressure-temperature range, and could potentially be used as a benchmark to compare various other pressure scales under high temperature conditions. - Graphical abstract: The saturation curve of SiO{sub 2} in TiO{sub 2} shows a strong pressure dependence and a strong dependence of unit cell volume on composition. This provides an opportunity to use this saturation curve as a measurement of pressure during a high-pressure experiment. The curve is a sensitive measure of pressure from 3 GPa to 10 GPa at high temperatures. The pressure is derived from lattice parameter measurements on the recovered solid solution, meaning that in-situ measurements are not necessary to evaluate the pressure of the experiment. - Highlights: • The unit cell of a saturated GeO{sub 2}–SiO{sub 2} solid solution is used as a pressure sensor. • We measure nine bracketed pressure points on the GeO{sub 2}–SiO{sub 2} saturation surface. • We provide a pressure calibrant from 3 GPa to 10 GPa at two temperatures. • Four points are measured at 1200 °C and five points at 1500 °C. • A thermodynamic model is developed for use of the calibrant at other temperatures.« less
NASA Astrophysics Data System (ADS)
Weber, Sebastian; Martinez, Raul
2016-04-01
The Western Alpine Penninic domain is a classical accretionary prism that formed after the closure of the Penninic oceans in the Paleogene. Continental and oceanic nappes were telescoped into the Western Alpine stack associated with continent-continent collision. Within the Western Alpine geologic framework, the ophiolite nappes of the Zermatt-Saas Zone and the Tsate Unit are the remnants of the southern branch of the Piemonte-Liguria ocean basin. In addition, a series of continental basement slices reported as lower Austroalpine outliers have preserved an eclogitic high-pressure imprint, and are tectonically sandwiched between these oceanic nappes. Since the outliers occur at an unusual intra-ophiolitic setting and show a polymetamorphic character, this group of continental slices is of special importance for understanding the tectono-metamorphic evolution of Western Alps. Recently, more geochronological data from the Austroalpine outliers have become available that make it possible to establish a more complete picture of their complex geological history. The Lu-Hf garnet-whole rock ages for prograde growth of garnet fall into the time interval of 52 to 62 Ma (Weber et al., 2015, Fassmer et al. 2015), but are consistently higher than the Lu-Hf garnet-whole rock ages from several other locations throughout the Zermatt-Saas zone that range from 52 to 38 Ma (Skora et al., 2015). This discrepancy suggests that the Austroalpine outliers may have been subducted earlier than the ophiolites of the Zermatt-Saas Zone and therefore have been tectonically emplaced into their present intra-ophiolite position. This points to the possibility that the Zermatt-Saas Zone consists of tectonic subunits, which reached their respective pressure peaks over a prolonged time period, approximately 10-20 Ma. The pressure-temperature estimates from several members of the Austroalpine outliers indicate a complex distribution of metamorphic peak conditions, without ultrahigh-pressure indications. By contrast, the peak conditions derived from the ophiolites of the Zermatt-Saas Zone are uniform, and close to or inside the coesite stability field. These results further underline that the oceanic lithosphere, which experienced its geodynamic evolution as a relatively coherent unit, may contain slices of continental rocks, which in turn show differences in the metamorphic evolution compared to the surrounding ophiolites. Faßmer, K., Obermüller, G., Nagel, T.J., Kirst, F., Froitzheim, N., Sandmann, S., Miladinova, I., Fonseca, R.O.C., Münker, C. (2015): Coherent vs. non-coherent subduction of ophiolite complexes - new insights from the Zermatt-Saas Zone in the Western Alps. GeoBerlin 2015, Berlin, Germany. Skora, S., Mahlen, N. J., Johnson, C. M., Baumgartner, L. P., Lapen, T. J., Beard, B. L., Szilvagyi, E. T., 2015. Evidence for protracted prograde metamorphism followed by rapid exhumation of the Zermatt-Saas Fee ophiolite. Journal of Metamorphic Geology, 33, 711-734. Weber, S., Sandmann, S., Fonseca, R. O. C., Froitzheim, N., Mu¨ nker, C., Bucher, K., 2015. Dating the beginning of Piemonte-Liguria Ocean subduction: Lu-Hf garnet chronometry of eclogites from the Theodul Glacier Unit (Zermatt-Saas Zone, Switzerland). Swiss Journal of Geosciences, 108, 183-199.
NASA Astrophysics Data System (ADS)
Bayet, Lea; Moritz, Lowen; Li, Jilei; Zhou, Tan; Agard, Philippe; John, Timm; Gao, Jun
2016-04-01
Subduction zone seismicity and volcanism are triggered by processes occurring at the slab-wedge interface as a consequence of metamorphic reactions, mass-transfer and deformation. Although the shallow parts of subduction zones (<30-40 km) can be partly accessed by geophysical methods, the resolution of these techniques is insufficient to characterize and image the plate interface at greater depths (>60km). In order to better understand the plate interface dynamics at these greater depths, one has to rely on the rock record from fossil subduction zones. The Chinese Tianshan metamorphic belt (TMB) represents an ideal candidate for such studies, because structures are well exposed with exceptionally fresh high-pressure rocks. Since previous studies from this area focused on fluid-related processes and its metamorphic evolution was assessed on single outcrops, the geodynamic setting of this metamorphic belt is unfortunately heavily debated. Here, we present a new geodynamic concept for the TMB based on detailed structural and petrological investigations on a more regional scale. A ~11km x 13km area was extensively covered, together with E-W and N-S transects, in order to produce a detailed map of the TMB. Overall, the belt is composed of two greenschist-facies units that constitute the northern and southern border of a large high-pressure (HP) to ultra high-pressure (UHP) unit in the center. This HP-UHP unit is mainly composed of metasediments and volcanoclastic rocks, with blueschist, eclogite and carbonate lenses. Only the southern part of the HP-UHP unit is composed of the uppermost part of an oceanic crust (e.g., pillow basalts and deep-sea carbonates). From south to north, the relative abundance and size of blueschist massive boudins and layers (as well as eclogite boudins) decreases and the sequence is increasingly interlayered with metasedimentary and carbonate-rich horizons. This indicates that the subducted material was dominated by trench filling made of sediments and volcanoclastic rocks, with only subordinate pieces of oceanic crust/lithosphere. The whole sequence is cut by km-scale major shear planes orientated WNW-ESE showing consistent top-to-the north shear senses. Lineations marked by glaucophane indicate that most of the deformation occurred during exhumation-related blueschist-facies conditions. Peak pressure and temperatures (P-T) were estimated by Raman spectroscopy, using the degree of organisation of carbonaceous material in metapelites for T and Raman peak shifts of quartz inclusions in garnets for P. In the whole HP-UHP region, consistent and homogeneous peak P-T conditions of 530±30°C and 2.3±3 GPa point to depths around 70 km and HP to UHP conditions, which is further supported by the local presence of coesite. The continuity of the lithological sequence and the lack of significant P/T offsets across the major shear planes indicate that, during exhumation, the HP-UHP unit primarily behaved as a single stack of essentially metasedimentary slices, and was only poorly dismembered on its way to the surface. Our study thus advocates for deep accretion/underplating and stacking of these tectonic slices (dominated by trench infill material) at depths of ~70 km, which has so far rarely been documented.
Chemical properties of Garnets from Garnet Ridge, Navajo volcanic field in the Colorado Plateau
NASA Astrophysics Data System (ADS)
Koga, I.; Ogasawara, Y.
2012-12-01
Significant amounts of garnet crystals have derived from kimberlitic diatremes at Garnet Ridge in northern Arizona. These garnets are chemically diverse and their origins have been still controversial. The diatremes at Garnet Ridge were dated at 30Ma (Smith et al., 2004). Coesite-bearing lawsonite eclogite reported by Usui et al., (2003) is important evidence for subduction of the Fallaron Plate below the Colorado plateau. This study characterized various kinds of garnets with several origins by petrographical observations and electron microprobe analyses (JXA-8900 WDS mode and JXA-733 EDS mode). On the basis of the chemical compositions and other features, the garnets were classified into the following 8 groups (A to H). Inclusions and exsolved phases were identified by laser Raman spectroscopy. (A) Garnet crystals (5-8 mm) with purple color are called ''Navajo Ruby''. A significant amount of Cr2O3 is a typical feature (up to ~5.9 wt. %). These garnet were rich in pyrope (66-78 mol. %). Olivine, Cpx, and exsolved lamellae of rutile were contained. (B) Reddish brown garnets were Pyp-rich (60-75 mol. %), and contained a minor amount of Cr2O3 (less than ~1 wt. %). The inclusions were rod-shaped rutile , Cpx, Opx, zircon, olivine and exsolved lamellae of apatite. (C) Garnet megacrysts (8-12 cm) were plotted near the center of Prp-Alm-Grs triangle (Pyp30-35 Alm28-33 Grs29-35). Exsolved apatite lamellae were confirmed. (D) Some of reddish brown garnets were plotted on same area as the Type-C. (E) Garnets in eclogite have Alm-rich composition (Pyp6-22 Alm52-65 Grs16-42). They clearly showed prograde chemical zonation; MgO: 1.4 to 5.4 wt. %, CaO: 14.0 to 5.6 wt. % both from core to rim. (F) Garnets in altered or metasomatized eclogite had a wide range of chemical composition (Pyp7-38 Alm52-69 Grs4-31) with similar prograde zonation. The cores were plotted near the rim of Type-E garnet. (G) Garnets in unidentified rock (strongly altered) had Alm-rich composition near Alm-Prp join. Euhedral quartz and zircon were included in the garnet. (H) Garnets in skarn-like rock of metasomatism origin at crustal level were plotted on Alm-Grs join and have no Prp component. Titanite, zoisite and fluid inclusion were identified in this garnet. Among the garnets described above, one of the typical garnets from Garnet Ridge is Cr-bearing Pyp-rich garnet, "Navajo Ruby", of peridotite origin at great depths, and another typical one is garnet in eclogite probably of subducted Farallon Plate origin. These two rocks having strong contrast each other were mixed underneath the Colorado Plateau. The chemical characteristics and petrographical features of the garnets from Garnet Ridge will give us very important information on complex petrochemical processes and related environments underneath the Colorado Plateau. Acknowledgements: The authors are grateful to Mrs. Pauline Deswudt who sold us various kinds of garnet grains and their host rocks for the present study. References: D. Smith, James N. Connelly, Kathryn Manser, Desmond E. Moser, Todd B. Housh, Fred W. McDowell, and Lawrence E. Mack., Vol. 5, Number 4. (2004) Geochemistry Geophysics Geosystems Usui, T., Nakamura, E., Kobayashi, K., Maruyama, S. and Helmstaedt, H. (2003) Geology, 31.
NASA Astrophysics Data System (ADS)
Mueller, H. J.; Schilling, F. R.; Lathe, C.
2004-05-01
The interpretation of seismic data from the Earth's deep interior requires measurements of the physical properties of Earth materials under experimental simulated mantle conditions. Elastic wave velocity measurement is an important tool for the determination of the elastic properties. Ultrasonic interferometry allows the highly precise travel time measurement at a sample enclosed in a high-pressure multi-anvil device. But the calculation of wave velocities requires the exact sample length under in situ conditions. There are two options - scanning the interfaces of the sample by XRD (Mueller et al., 2003) and X-radiography (Li et al., 2001). The multi-anvil apparatus MAX80 is equipped for both methods. Only the X-radiography is fast enough for transient measurements. Contrary to XRD measurements, imaging the sample by X-rays requires a beam diameter larger than the sample length. Therefore the fixed primary slits of Max80 were exchanged by 4-blade high precision slits of Advanced Design Consulting, Inc. A Ce-YAG-crystal converts the X-ray image to an optical one, redirected by a mirror and captured by a CCD-camera. To derive the sample length, the different brightness of sample, buffer rod and reflector at the electronic image is evaluated. Classical ultrasonic interferometry is very time consuming, because the ultrasonic waves of the frequency range under study are generated and detected one after another with a given step rate. A 60 MHz frequency sweep with 100 kHz steps lasts for more than 30 minutes. This is a serious limitation for all transient measurements, but also limits the data collection at elevated temperatures to prevent the pressure transmitting boron epoxy cubes and the anvils from overheating. The ultrasonic transfer function technique (UTF), first described by Li et al. (2002), generates all the frequencies simultaneously. Related to the results and experiences of Li the UTF-technique was developed independently at GFZ. This version allows to consider the characteristics of the specific transducer-glue-anvil combination (Mueller et al., 2003). To collect the data for the following calculation of Vp and Vs requires just few seconds. The excitation function, applied to the transducer by an arbitrary waveform generator, is the result of the summation of all sinusoidal waves inside the frequency range. The response of the system - transducer - anvil - buffer rod - sample - reflector - for each of the frequencies can be reproduced by convoluting the resulting transfer function with these monochromatic waves step by step. Some recent results on the non-quenchable high-P - low-P clinoenstatite transition and to the quartz-coesite transition will be given to discuss the different interferometric techniques, including the XRD-data and X-radiography results, necessary to detect the phase transitions under in situ conditions and to measure the sample deformation. Li, B.; Vaughan, M.T.; Kung, J.; Weidner, D.J., NSLS Activity Report 2001, 2-103-106, (2001). Li, B.; Chen, K.; Kung, J.; Liebermann, R.C.; Weidner, D.J., J. Phys.: Condens. Matter 14, 11337-11342, (2002). Mueller, H.J.; Schilling, F.R.; Lauterjung, J.; Lathe, C., Eur. J. Mineral., 15, 865-873, (2003). Mueller, H.J.; Wunder, B.; Lathe, C.; Schilling, F.R.; Eur. J. Mineral., submitted, (2004).
NASA Astrophysics Data System (ADS)
Little, T. A.; Hacker, B.; Seward, G.
2008-12-01
The up to ~2.5 km-high gneiss domes of the NW D'Entrecasteaux Islands of Papua New Guinea host the world's youngest terrane of HP (eclogite-facies, ~2-4 Ma) to UHP (coesite-bearing) gneissic rocks (~8 Ma). Previous models for their exhumation at >2 cm/yr have called upon: 1) buoyant rise of crustal diapers, or 2) normal-slip on deeply penetrating faults. A recent variant of the latter suggests that a paleo- subduction zone near the southern edge of the Solomon Sea has been inverted as a result of microplate tectonics. We present structural, microstructural, and electron back-scatter diffraction data of lattice preferred orientations (LPO's) from gneisses of Goodenough and Fergusson Islands to further explore mechanisms of exhumation. Relict eclogite-facies assemblages occur in mafic dikes and boudins, but most HP deformational fabrics are overprinted. The enclosing felsic gneisses are pervaded by amphibolite-facies ductile fabrics formed during their exhumation from the lower crust. These migmatitic rocks (metatexites) were partially molten during their deformation at temperatures of 570-730°C and pressures of 7-11 kb, but today are dominated by solid-state fabrics. The gneisses are capped by remnants of an ultramafic sheet that did not experience HP metamorphism. Below the ultramafics is a ~1 km-thick carapace zone. These high-strain gneisses generally have domal fabrics parallel to, and gradational to, those in the underlying core zone, which they locally rework. Active NE-dipping normal faults on the NE flank of the domes cut across the ultramafic contact and are underlain by a m-thick zone of pseudotachylite-bearing S/C fabrics. A sweeping pattern of stretching lineations reveals a 3-D pattern of ductile flow. In both the carapace and upper core zone, lineations are mostly EW: subparallel to the long dimension of the domes and perpendicular to plate motion in the Woodlark Rift. At greater structural depth, within the core zone, they deflect to become more nearly plate-motion parallel. Shear indicators diverge across the dome crests, suggesting of an inward flow of deeper rocks into the dome; or are locally variable, consistent with bulk irrotational deformation. In the gneisses (both core and carapace), conjugate shear-band microstructures and near-orthorhombic quartz LPOs, and back-rotation of mantled porphyroclasts indicate that ductile strain in domes was near plane, but that it was not simple shear (and included significant vertical shortening). The LPO's of the deepest rocks record activity of the high-T prism-[c] and prism- slip systems, whereas the outermost carapace rocks record basal- and rhomb- slip. The data reveal that deformational temperatures increased toward the dome centers, rather than outwardly into the carapace. Quartz LPO's in both dome and carapace are of uniformly modest intensity (~2-3 times random). Feldspar LPO's suggest slip on the (010)[001] or (010)[100] systems, and in some cases a shear sense opposite to quartz. While we cannot resolve how the eclogitic rocks ascended isothermally from the mantle into the lower crust, the simplest model invokes diapiric ascent (with decompression melting), ponding and lateral spreading along the Moho during early Woodlark Basin rifting. Subsequent exhumation of these rocks from the lower crust involved continued upward movement and vertical shortening of the gneisses combined with subhorizontal rift-parallel flow. Finally, normal faulting and minor erosion exhumed these rocks through the ultramafic cover to their present levels.
Partial melting of carbonated pelite at 3-7 GPa and deep cycling of CO2 and H2O in subduction zones
NASA Astrophysics Data System (ADS)
Tsuno, K.; Dasgupta, R.; Danielson, L. R.; Righter, K.
2011-12-01
The exchange of water and carbon dioxide between the Earth's crustal rocks and the interior is important for understanding geochemical and geophysical evolution of the planet on geologic timescale. Subduction of pelitic sediments is a key mechanism for volatile introduction to the mantle but the high-pressure behavior of H2O+ CO2 bearing sediments is only constrained for alumina-rich, low-Mg# bulk compositions [1, 2]. However, the ocean-floor sediments for many subduction zones that contain both water and CO2 are alumina-poor and have higher Mg#. To constrain the melting behavior of a model alumina poor carbonated pelite, we performed new experiments. Piston cylinder (3 GPa) and multianvil (5 and 7 GPa) experiments were conducted between 800 and 1150 °C, using a model sediment composition containing 1 wt.% H2O and 5 wt.% CO2 (trace vapor-present at subsolidus conditions). The choice of the bulk composition was aimed to model the loss of siliceous hydrous fluid during the shallow part of subduction. We determined the solidus temperatures between 800 and 850 °C at 3 GPa, 900 and 950 °C at 5 GPa, and <1000 °C at 7 GPa. The subsolidus phases include cpx, garnet, coesite, rutile, phengite, and calcitess at 3 GPa, and kyanite comes in at 5 GPa. Hydrous rhyolitic silicate melt was observed at 3 GPa and up to 1150 °C. The near-solidus melt at 5-7 GPa was K-rich and calcio-carbonatitic, in contrast to the previous experimental results in alumina-rich and low Mg# bulk composition [1, 2], which showed the stability of Al-rich trachyitic silicate melt at near-solidus temperatures up to 5 GPa, and replaced by carbonate melt only at ≥5.5 GPa. Carbonate-silicate melt immiscibility was observed at 5 GPa, 1100 °C in our study. The phengite-out boundary is located between 850 and 900 °C at 3 GPa, between 1000 and 1100 °C at 5 GPa, and <1000 °C at 7 GPa. The crystalline carbonate-out boundary is between 950 and 1000 °C at 3 and 5 GPa, and <1000 °C at 7 GPa. Comparison of our results, in terms of the P-T locations of the solidus, phengite- and carbonate-out boundaries, to the thermal structures of the slab-surface in cold-intermediate subduction zones indicates that most of the phengite-bound H2O and carbonate-bound CO2 are recycled into the deep upper mantle (~200 km depth). On the other hand, substantial amounts of C-O-H volatiles, in the form of either hydrous silicate melt or K-rich calcio-carbonatitic melt, are likely to be released from relatively hot subducting slabs. The observation of carbonate melt inclusion in cpx and garnet in deeply subducted carbonate-rich sediments [3] might be explained by our experimental results that carbonatite is the stable near-solidus sediment melt at deep sub-arc depths. [1] Thomsen, T.B. and Schmidt, M.W. 2008, EPSL 267, 17-31. [2] Grassi, D. and Schmidt, M.W. 2011, J. Petrol. 52, 765-789. [3] Korsakov, A.V., and Hermann, J. 2006, EPSL, 104-118.
Surface geology of the Jeptha Knob cryptoexplosion structure, Shelby County, Kentucky
Cressman, Earle Rupert
1981-01-01
The Jeptha Knob crytoexplosion structure, described by Bucher in 1925, was remapped in 1973 as part of the U.S. Geological Survey and the Kentucky Geological Survey cooperative mapping program. The knob is in the western part of the Blue Grass region. Hilltops in the rolling farmland adjacent to the knob are underlain by the nearly flat-lying Grant Lake and Callaway Creek Limestones of middle Late Ordovician age, and the valleys are cut in interbedded limestone and shale of the Clays Ferry Formation of late Middle and early Late Ordovician age. Precambrian basement is estimated to be 4,000 ft below the surface. The mapped area is 50 miles west of the crest of the Cincinnati arch; the regional dip is westward 16 ft per mile. The 38th parallel lineament is 50 miles to the south. The structure, about 14,000 ft in diameter, consists of a central area 6,300 ft in diameter of uplifted Clays Ferry Formation surrounded by a belt of annular faults that are divided into segments by radial faults. The grass structure of the Clays Ferry Formation is that of a broad dame, but same evidence indicates that, in detail, the beds are complexly folded. The limestone of the Clays Ferry is brecciated and infiltrated by limonite. The brecciation is confined to single beds, and there is no mixing of fragments from different beds. A small plug of the Logana Member of the Lexington Limestone (Middle Ordovician) has been upfaulted at least 700 ft and emplaced within the Clays Ferry. The central uplift is separated by high-angle and, in places, reverse faults from the belt of annular faulting. The concentric faults in the zone of annular faults are extensional, and the general aspect is of collapse and inward movement. Lenses of breccia are present along many of the concentric faults, but not along the radial faults. At least same of the breccia was injected from below. The youngest beds involved in the faulting are in the Bardstown Member of the Drakes Formation of late Late Ordovician age. The faulted and brecciated beds are overlain by nearly horizontal dolomite and shale of Early and Middle Silurian age. The basal 5 ft of the oldest Silurian unit, the Brassfield Formation, contains calcarenite and calcirudite composed, in large part, of locally derived fragments from the Upper Ordovician formations. The Jeptha Knob structure was formed in latest Late Ordovician or earliest Early Silurian time. At the time of formation, the area was either very slightly above or very slightly below sea level; the sediments were already largely indurated. At the onset of Silurian deposition, the area of the central uplift was probably a broad shallow depression not more than about 15 ft deep, possibly surrounded by a rim of Upper Ordovician rocks or rock fragments. The origin of the Jeptha Knob structure cannot be determined from the available data. Shatter cones and coesite, considered by many to be definitive criteria far origin by impact, have not been found. On the other hand, geophysical studies indicate that there is no coincident uplift of the basement, and there is no certain relation of Jeptha Knob to any obvious structural trend.
Physical processes of quartz amorphization due to friction
NASA Astrophysics Data System (ADS)
Nakamura, Y.; Muto, J.; Nagahama, H.; Miura, T.; Arakawa, I.; Shimizu, I.
2011-12-01
Solid state amorphization of minerals occurs in indentations, in shock experiments, and in high pressure metamorphic quartz rock. A production of amorphous material is also reported in experimentally created silicate gouges (Yund et al., 1990), and in San Andreas Fault core samples (Janssen et al., 2010). Rotary-shear friction experiments of quartz rocks imply dynamic weakening at seismic rates (Di Toro et al., 2004). These experiments have suggested that weakening is caused by formation and thixotropic behavior of a silica gel layer which comprises of very fine particles of hydrated amorphous silica on fault gouges (Goldsby & Tullis, 2002; Hayashi & Tsutsumi, 2010). Therefore, physical processes of amorphization are important to better understand weakening of quartz bearing rocks. In this study, we conducted a pin-on-disk friction experiment to investigate details of quartz amorphization (Muto et al, 2007). Disks were made of single crystals of synthetic and Brazilian quartz. The normal load F and sliding velocity V were ranged from 0.01 N to 1 N and from 0.01 m/s to 2.6 m/s, respectively. The friction was conducted using quartz and diamond pins (curvature radii of 0.2 ~ 3 mm) to large displacements (> 1000 m) under controlled atmosphere. We analyzed experiment samples by Raman spectroscopy and FT-IR. Raman spectroscopy (excitation wavelength 532.1 nm) provides lattice vibration modes, and was used to investigate the degree of amorphization of samples. Raman spectra of friction tracks on the disk show clear bands at wavenumbers of 126, 204, 356, 394, and 464 cm-1, characteristic of intact α-quartz. Remarkably, in experiments using diamond pins (F = 0.8 N, normal stress σr calculated by contact area = 293 ~ 440 MPa, V = 0.12 ~ 0.23 m/s), the bands at 204 and 464 cm-1 gradually broaden to reveal shoulders on the higher-wavenumber sides of these peaks. Especially, two distinguished peaks at 490 and 515 cm-1 and a weak broad peak at 606 cm-1 appear sporadically on the track after the slip distance of 43 m. The bands at 490 and 606 cm-1 can be assigned to the symmetric stretching of four-membered Si-O ring (D1 band) and planar three-membered Si-O ring (D2 band) in amorphous silica, respectively. The peak at 515 cm-1 corresponds to the strongest coesite A1 mode arising from four-membered Si-O ring structure. On the other hand, the bands at 464 cm-1 broaden to reveal a shoulder adjacent to the main peak in experiments using quartz pins (F = 1 N, σr = 1 MPa, V = 0.01 ~ 2.6 m/s) after a large displacement (>1000m). These results indicate that quartz change intermediate range structure of SiO2 network during friction, and four or three-membered Si-O rings gradually increase in six-membered quartz. The results of FT-IR analyses on friction tracks showed a broad peak at 3000 -3600 cm-1 which indicates the -OH symmetric stretching band of molecular H2O. It shows that hydration of quartz on friction tracks occur due to friction. The results of Raman spectroscopy and FT-IR imply that Si-O-Si bridging of strained rings preferentially react with water to form hydrated amorphous silica layer on friction surfaces, which is likely to occur weakening.
NASA Astrophysics Data System (ADS)
Blundy, J.; Skora, S.
2009-12-01
A global correlation between the incompatible trace element chemistry of subducted sediments and that of magmas erupted through the overlying plate testifies to the important role that sediments play in controlling magmagenesis. We report new experimental data on the high pressure (3 GPa) and temperature (700-1300 °C) phase relations of hydrous red clay to evaluate the role of residual accessory phases in controlling the incompatible trace element chemistry of sediment-derived fluids. A particular focus is monazite, which preferentially incorporates LREE and Th, exerting a powerful control on the fluid Th/LREE ratio. Given that arc magmas appear to inherit the Th/LREE ratio of the associated subducting sediment, understanding monazite solubility and stability has the potential to provide new constraints on temperature at the slab surface, a parameter that is notoriously hard to pin down by other means. Experiments on red clay with H2O structurally bound in hydrous minerals (<2 wt%) produced negligible melt fractions for any reasonable temperatures. Experiments with 7-15 wt% added H2O produced copious melting at temperatures only 50-100°C above the solidus (c. 720 °C), e.g. with 15 wt% added H2O, the red clay is >50% molten at 800 °C. Irrespective of the amount of added H2O the residual assemblage comprised garnet and kyanite up to the liquidus (1250 °C with 7 wt% H2O). Phengite is present ≤800 °C; ilmenite and rutile persist to c. 1000 °C; quartz/coesite-out temperature decreases from 1000 °C with 7 wt% H2O to 800 °C with 15%. Monazite was stable to 950 °C in the Th- and LREE-doped starting materials that we used. The trace element contents of the residual melts in equilibrium with monazite-thorite solid solutions were used, in conjunction with published data, to develop a thermodynamic model of LREE and Th solubility in sediment-derived fluids. These models were used to calculate the stability of monazite in a red clay with natural LREE and Th levels. For the case of 7 wt% added H2O, monazite is exhausted at 825 °C; it disappears at 780 °C with 15 wt% added H2O. In our experiments monazite fractionates LREE from Th, such that fluids preserving the original sedimentary ratio must be generated at or above monazite-out temperatures in subducted slabs where red clay is the dominant sedimentary lithology. We propose that the subducted sedimentary signature is imparted by fluxing of H2O derived from hydrated (e.g. serpentinised) portions of the deeper subducting slab, triggering copious “flash melting” of the sediment at the point were its temperature exceeds ~800 °C. Without the addition of H2O sediment melting is too restricted to allow any appreciable fluid release into the overlying mantle. Moreover, under such conditions the Th/LREE ratio is strongly fractionated due to the abundance of residual monazite. The availability of H2O in hydrated portions of subducted slabs, e.g. in the vicinity of fracture zones, may exercise an important control on the spatial distribution of subduction zone magmatism.
Is the X-discontinuity really related to the presence of eclogite bodies in the mantle?
NASA Astrophysics Data System (ADS)
Woodland, Alan; Knapp, Nadia; Klimm, Kevin
2013-04-01
A local seismic feature observed at ~300 km depth is referred to as the X-discontinuity (X-disc, e.g. Revenaugh & Jordan 1991). Several petrological explanations have been proposed for this discontinuity, but Pushcharovsky & Pushcharovsky (2012) attribute it to the formation of stishovite in eclogitic bodies, based upon the suggestion of Williams & Revenaugh (2005). If this link between the X-disc and the presence of eclogite is valid, it could have important geodynamic implications. In their model, stishovite appears in the eclogitic assemblage either through the transformation of previously existing free coesite or by exsolution of "excess" SiO2 from Ca-Eskola-bearing clinopyroxene (Ca0.50.5Si2O6). Essential to this model is if the amount of free SiO2 is enough to produce the observed seismic impedance contrast or not. To test whether exsolution of stishovite from Ca-Eskola-bearing clinopyroxene is a feasible mechanism, we have undertaken high-pressure experiments to determine the maximum Ca-Eskola component that can be incorporated in clinopyroxene over a range of P-T conditions, both shallower and deeper than that corresponding to the position of the X-disc. One series of experiments were performed in the simplified CaO-MgO-Al2O3-SiO2±Na2O system and one with 3 "natural" analog eclogite compositions (K2O-Na2O-CaO-MgO-FeO-Al2O3-SiO2). For the CMAS-experiments, all samples have the typical eclogitic assemblage of clinopyroxene + garnet ± SiO2 ± kyanite. With increasing pressure, the amount of garnet increases at the expense of clinopyroxene. Maximizing the Ca-Eskola content of clinopyroxene requires coexistence with a free SiO2 phase and an elevated Al2O3 content, but not necessarily the presence of kyanite. Ca-Eskola contents of ~20 mol % are obtained at 4 GPa, but decrease steadily with increasing pressure so that ˜ 4 mol % is present at pressures corresponding to the depth of the X-disc. Experiments in natural analog eclogite compositions produced even less Ca-Eskola component in clinopyroxene. Thus no sharp change in Ca-Eskola content occurs as a function of pressure and at depths corresponding to the X-discontinuity exsolution of all Ca-Eskola component will yield only < 1 wt% free SiO2. This amount is insufficient to produce a large enough impedance contrast to explain the X-disc. If the X-disc is related to the appearance of stishovite in eclogite as proposed by Williams & Revenaugh (2005), then free SiO2 must be already present in the mineral assemblage. However, our preliminary results suggest that in an unmodified MORB-type eclogite only minor amounts of free SiO2 will be present. Greater amounts of free SiO2 can only be reached in eclogite residues after melt extraction at high pressures of ~5 GPa, where as residues from melting at lower pressures (i.e. 2.5 GPa) do not produce any free SiO2. Therefore, if at all, only subducted oceanic crust that first experienced melting at high pressures can contain enough free SiO2 to produce the observed impedance contrast of the X-disc as it transforms to stishovite. Pushcharovsky DY & Pushcharovsky YM (2012) Earth-Sci Revs, 113, 94-109. Revenaugh J & Jordan TH (1991) J Geophys Res, 96, 19,781- 19,810, Williams Q & Revenaugh J (2005) Geology, 33, 1-4.
NASA Astrophysics Data System (ADS)
Brown, M.
2006-12-01
Essene's contributions began pre-plate tectonics more than 40 years ago; they range from mineralogy to tectonics, from experiments and thermobarometry to elements and isotopes, and from the Phanerozoic to the Precambrian. Eric is a true polymath! Assessing the P-T conditions and age distribution of crustal metamorphism is an important step in evaluating secular change in tectonic regimes and geodynamics. In general, Archean rocks exhibit moderate-P - moderate-to-high-T facies series metamorphism (greenstone belts and granulite terranes); neither blueschists nor any record of deep continental subduction and return are documented and only one example of granulite facies ultrahigh-temperature metamorphism is reported. Granulite facies ultrahigh temperature metamorphism (G-UHTM) is documented in the rock record predominantly from Neoarchean to Cambrian, although G-UHTM facies series rocks may be inferred at depth in younger orogenic systems. The first occurrence of G-UHTM in the rock record signifies a change in geodynamics that generated transient sites of very high heat flow. Many G-UHTM belts may have developed in settings analogous to modern continental backarcs. On a warmer Earth, the formation and breakup of supercontinents, particularly by extroversion, which involved destruction of ocean basins floored by thinner lithosphere, may have generated hotter continental backarcs than those around the modern Pacific rim. Medium-temperature eclogite - high-pressure granulite metamorphism (E-HPGM) also is first recognized in the Neoarchean rock record, and occurs at intervals throughout the Proterozoic and Paleozoic rock record. E- HPGM belts are complementary to G-UHTM belts, and are generally inferred to record subduction-to-collision orogenesis. Blueschists become evident in the Neoproterozoic rock record; lawsonite blueschists and eclogites (high-pressure metamorphism, HPM), and ultrahigh pressure metamorphism (UHPM) characterized by coesite or diamond are predominantly Phanerozoic phenomena. HPM-UHPM registers low thermal gradients and deep subduction of continental crust during the early stage of the collision process in Phanerozoic subduction-to-collision orogens. Although counterintuitive, many HPM-UHPM belts appear to have developed by closure of small ocean basins in the process of accretion of a continental terrane during a period of supercontinent introversion (Wilson cycle ocean basin opening and closing). A duality of metamorphic belts - reflecting a duality of thermal regimes - appears in the record only since the Neoarchean Era. A duality of thermal regimes is the hallmark of modern plate tectonics and the duality of metamorphic belts is the characteristic imprint of plate tectonics in the rock record. The occurrence of both G- UHTM and E-HPGM belts since the Neoarchean manifests the onset of a `Proterozoic plate tectonics regime', although the style of tectonics likely involved differences from modern Earth. Although the style of Proterozoic subduction remains cryptic, the change in tectonic regime whereby interactions between discrete lithospheric plates generated tectonic settings with contrasting thermal regimes was a landmark event in Earth history. The `Proterozoic plate tectonics regime' evolved during a Neoproterozoic transition to the `modern plate tectonics regime' characterized by colder subduction, and subduction of continental crust deep into the mantle and its (partial) return from depths of up to 300 km, as chronicled by the appearance of blueschists and HPM-UHPM in the rock record.
NASA Astrophysics Data System (ADS)
Bukała, Michał; Majka, Jarosław; Walczak, Katarzyna; Barnes, Christopher; Klonowska, Iwona
2017-04-01
The Seve Nappe Complex (SNC) of the Scandinavian Caledonides has well documented history of high pressure (HP) and ultra-high pressure (UHP) metamorphism (e.g. Klonowska et al. 2014). Eclogites of the SNC occur in two areas in Sweden, namely Jämtland and Norrbotten. The Jämtland eclogites and associated rocks are well studied and provide evidence for the Late Ordovician UHP metamorphism, whereas the Norrbotten eclogites, formed during the Late Cambrian/Early Ordovician, have not been studied in detail, especially in terms of pressure-temperature (P-T) conditions of their formation. Within the SNC in Norrbotten, eclogites are limited to two tectonic lenses - Vaimok and Tsäkkok (e.g. Albrecht, 2000). Within the Vaimok Lens three nappes have been distinguished: (1) the eclogite-free Lower Seve Nappe, (2) the Grapesvåre Nappe and (3) the Maddåive Nappe. The two latter nappes are eclogite-bearing. For this study eclogites were collected from the lowermost part of the Grapesvåre Nappe (from the highly heterogeneous Daunasvagge unit dominated by garnet-bearing mica schists, quartzites and marbles). Eclogite boudins (former dolerite dikes and sills) are usually highly altered due to retrogressive recrystallization. Rare fresh eclogites occur within large boudins (>5m in diameter) and display only minor alteration limited to the scarce veinlets composed of amphibole + feldspar + garnet + zoisite + biotite + rutile + titanite. Metamorphic peak conditions mineral assemblage consists of garnet + omphacite + phengite + quartz + rutile. For P-T estimates the geothermobarometric method of Ravna & Terry (2004) has been used. The garnet-clinopyroxene Fe2+-Mg exchange thermometer and the net-transfer reaction barometer based on the garnet-phengite-omphacite equilibrium yielded a maximum pressure of 26.7 kbar and temperature of 677°C. The obtained temperature might be underestimated due to uncertainties in Fe2+/Fe3+ ratio in pyroxene. Therefore Zr-in-rutile geothermometer by Tomkins et al. (2007) has also been used and calculcated temperatures are in a 715-762°C range. The obtained results are somewhat similar to scarce former P-T estimates of eclogites from Norrbotten provided by Santallier (1988) (i.e. T=690-730°C and Pmin=18.5-19.5 kbar) and Albrecht (2000) (i.e. T=650-720°C and P=18.9-27.5 kbar). However, as Albrecht (2000) claimed, pressure values might have been largely underestimated due to limitation of the used methods. Thus our study provides for the first time an evidence for near UHP metamorphism recorded by eclogites of the Grapesvåre Nappe, hence shedding a new light on evolution of the SNC in Norrbotten. We speculate that maximum pressures of metamorphism might have been higher (even approaching coesite stability field), but further studies are required to pinpoint the maximum PT conditions. This work is financially supported by the NCN "CALSUB" research project no. 2014/14/E/ST10/00321. References: Albrecht L.G. (2000) PhD thesis, Lund University. Klonowska I., Majka J., Janák M., Gee D.G., Ladenberger A. (2014) New Perspectives on the Caledonides of Scandinavia and Related Areas. Geological Society, London, Special Publications, 390: 321-336. Ravna E.J., Terry M.P. (2004) Journal of Metamorphic Geology 22: 579-592. Santallier D.S. (1988) Geologiska Föreningen i Stockholm Förhandlingar 110: 89-98. Tomkins H.S., Powell R., Ellis J.D. (2007) Journal of Metamorphic Geology 25: 703-713.
Tectonic Activity and Processes Preceding the Formation of the Dead Sea Fault Zone
NASA Astrophysics Data System (ADS)
Eppelbaum, L. V.; Pilchin, A. N.
2007-12-01
Analysis of geological-geophysical data indicates that at the end of the Proterozoic, blocks of the Arabian Shield (AS) were thrust to the north-west onto the crust of the proto-Mediterranean (PM). This was caused by the pushing of oceanic crust from the south-east forming the Najd faults system (NF). This thrusting took place between 630 and 590 Ma, and is confirmed by the offsets between the Yanbu suture of the AS and Allaqi-Sol Hamid suture of the Nubian Shield (NS), the Bi'r Umq suture of AS and Nakasib suture of NS, and parts of the Yanbu and Nabitah sutures of AS. This caused the separation of AS from NS, and AS from the continental crust to north-east of it with its north-western displacement, resulting in opening of the Persian Gulf. This caused the start of deposition of huge amounts of Vendian-Cambrian evaporites in Saudi Arabia, Oman, Persian Gulf, Zagros, central Iran and other regions. The fact of the formation and preservation of the evaporites, and the common similarities in Vendian-Triassic sedimentary cover of Central Iran, Zagros, Taurus, and Arabian Plate (AP) and common Late Proterozoic-Early Paleozioc magmatic activity, show that these regions did not change their position significantly since then. Results of the DESERT project show that the lowermost part of the crust is present east of the Dead Sea Fault Zone (DSFZ), but it is absent west of it. This could be explained by detachment of the bottom part of the crust west of DSFZ during AP thrusting onto the crust of PM. The lithospheric slice discovered by seismic data between Moho and depth of about 55 km in S. Israel could be a remnant of that crust. During the thrusting, the AP overrode the detached slice. The slice was later remelted during formation of the postorogenic magmatic rocks of 590-530 Ma widespread in Jordan. The formation of three dyke swarms in S. Israel (600-540 Ma), widespread dykes in Sinai (590-530 Ma) and AP (590-530 Ma), as well as high-T-low-P metamorphism between 600 and 530 Ma, point to a huge release of heat likely caused by friction during the thrusting. Presence of giant quantities of K-rich granites also points to reworking of continental crust in the region. Small amount of magmatic formations younger than Cambrian age west of DSFZ and significant amount of magmatic formations of this period east of DSFZ also indicate to presence of the plate beneath Israel. Offset of suture zones within AS shows that displacement was maximal for the northern blocks of AS. This is in agreement with known separation of Israel's crust into three blocks: Negev, Judea-Samaria and Galilee- Lebanon. Numerous markers of high to ultra-high pressure conditions signify to collision between the AP and the PM. These markers are: iron rich aegerine-augite and olivine-rich phenocrysts in S. Israel; peridotite xenoliths in S. Israel equilibrated at depth ~33-34 km; discovery of diamonds, micro-diamonds and indicator minerals (Cr- diopside, orange garnet, pyrope, coesite, picroilmenite, moissanite, carbonado, corundum, olivine, perovskite, aegerine, Ti-augite) in S. Israel; garnet clinopyroxenites, garnet granulites, indicator minerals, and eclogite-like rocks in Mt. Carmel area of N. Israel; iron-rich garnets in Sinai; eclogites, diamonds and indicator minerals in non-kimberlite environments in Syria; ophiolites exposed in Syria at northern extension of the DSFZ; ophiolite-like rocks in Sinai. These markers are located along or in close proximity to the DSFZ. Different isostatic conditions east of the edge of- and above- the underlying plate, along with the eventual activation of the plate caused the later formation of the DSFZ.
Effect of crustal heterogeneities and effective rock strength on the formation of HP and UHP rocks.
NASA Astrophysics Data System (ADS)
Reuber, Georg; Kaus, Boris; Schmalholz, Stefan; White, Richard
2015-04-01
The formation of high pressure and ultra-high pressure rocks has been controversially discussed in recent years. Most existing petrological interpretations assume that pressure in the Earth is lithostatic and therefore HP and UHP rocks have to come from great depth, which usually involves going down a subduction channel and being exhumed again. Yet, an alternative explanation points out that pressure in the lithosphere is often non-lithostatic and can be either smaller or larger than lithostatic as a function of location and time. Whether this effect is tectonically significant or not depends on the magnitude of non-lithostatic pressure, and as a result a number of researchers have recently performed numerical simulations to address this. Somewhat disturbingly, they obtained widely differing results with some claiming that overpressures as large as a GPa can occur (Schmalholz et al. 2014), whereas others show that overpressures of exhumed rocks are generally less than 20% and thus insignificant (Li et al. 2010; Burov et al. 2014). In order to understand where these discrepancies come from, we reproduce the simulations of Li et al (2010) of a typical subduction and collision scenario, using an independently developed numerical code (MVEP2). For the same model setup and parameters, we confirm the earlier results of Li et al. (2010) and obtain no more than ~20% overpressure in exhumed rocks of the subduction channel. Yet, a critical assumption in their models is that the subducted crust is laterally homogeneous and that it has a low effective friction angle that is less than 7o. The friction angle of (dry) rocks is experimentally well-constrained to be around 30o, and low effective friction angles require, for example, high-fluid pressures. Whereas high fluid pressures might exist in the sediment-rich upper crust, they are likely to be much lower or absent in the lower crust from which melt has been extracted or in rocks that underwent a previous orogenic cycle. In a next step, we performed several hundred numerical simulations to understand the effects of km-scale heterogeneities and material parameters on pressure magnitudes, using a model setup that is otherwise very similar to the one of Li et al. (2010). Results show that significant non-lithostatic pressures occur if (lower) crustal rocks are dry or if km-scale (nappe-sized) heterogeneities with dryer rocks are present within the crust. Overpressure magnitudes can be up to 1 GPa or 100% and in some cases rock assemblages are temporarily in the coesite stability field at a depth of only 40 km, followed by rapid exhumation to the surface. Tectonic overpressures can vary strongly in magnitude versus time, but peak pressures are present sufficiently long for metamorphic reactions to occur. The presence of heterogeneities can affect the crustal-scaled deformation pattern, and the effective friction angle of crustal-scale rocks (or the dryness of these rocks) is a key parameter that determines the magnitude of non-lithostatic pressures. Our results thus reconcile previous findings and highlight the importance of having an accurate knowledge of the fluid-pressure, initial crustal structure and rock composition during continental collision. If rocks are dry by the time they enter a subduction zone, or are stronger/dryer than surrounding rocks, they are likely to develop significantly higher pressures than nearby rocks. This might explain the puzzling observation that some nappes have very high peak pressures, while juxtaposed nappes have much lower values, without clear structural evidence for deep burial and exhumation along a subduction channel of the high-pressure nappe. Our models might also give a partial explanation of why the reported timescales for high and ultra-high pressure stages of peak metamorphism are often very short. References: Burov, E., Francois, T., Agard, P., Le Pourhiet, L., Meyer, B., Tirel, C., Lebedev, S., Yamato, P., Brun, J.-P., 2014. Tectonophysics. Tectonophysics 631, 212-250. doi:10.1016/j.tecto.2014.04.033 Li, Z.H., Gerya, T.V., Burg, J.-P., 2010. Influence of tectonic overpressure on P-T paths of HP-UHP rocks in continental collision zones: thermomechanical modelling. J Metamorph Geol 28, 227-247. doi:10.1111/j.1525-1314.2009.00864.x Schmalholz, S.M., Duretz, T., Schenker, F.L., Podladchikov, Y.Y., 2014. Tectonophysics. Tectonophysics 631, 160-175. doi:10.1016/j.tecto.2014.05.018
NASA Astrophysics Data System (ADS)
Ashchepkov, Igor; Logvinova, Alla; Spetsius, Zdislav; Ntaflos, Theodoros; Ravi, Subramanaian; Vladykin, Nikolai; Stegnitsky, Yuri; Babushkina, Svetlana; Ovchinnikov, Yuri
2016-04-01
Enhanced monomineral thermobarometry for clinopyroxenes and garnet (Ashchepkov et al., 2015) allow reconstruction of thermal conditions for the mantle eclogitic xenoliths and xenocrysts of omphacites and pyrope almandine garnets of eclogitic and megacrystic types. Three common groups according to Dawson,(1977) A. Mg - eclogites; B. common subduction-related basaltic eclogites and C. Na-Fe- rich eclogites. In addition group D compile Ca-Al rich varieties (Spetsius et al., 2008; Viljoen et al., 2010). We subdivided these groups and their positions in mantle lithosphere sections beneath the most studied pipes in Yakutia and most interesting localities Worldwide. Group A including Al-rich and low groups are restites or cumulates from the ancient komatiitic basalts or boninites. The Fe# for olivine in equilibrium is 0.05 -0.11 using melt -solid partition coefficient ~0.33 for Fe (Albarede, 1992). For the group B Fe# of the omphacites are ~ 0.11- 0.23 and they could be only cumulates from melted subducted MORB basalts or reactional products. The higher values of Fe -Na-Al rich group C (Fe# ~0.25-0.4) could relate to the subducted basalts or Al - rich sediments (Spetsius et al., 2008) or Mg-rich crustal rocks which were subducted without much melting. Group D Ca-rich eclogites are commonly low Fe but subduction related varieties (Dongre et al., 2015) could be higher in Fe and Na. Partition coefficients of the trace elements between Gar and Cpx for most mantle eclogites relate to equilibration with the melts and REE patterns show different inclinations, while crustal eclogites which re-equilibrated in the solid state often show the same inclinations. Groups A1: a Cr-bearing group formed after crystallization of partial melts produced by volatile fluxes generated by ancient subduction (Heaman et al., 2006; Smart et al., 2009); A2 - low - Al cumulates and restites from komatiitic melts (Aulbach et al., 2011); A3 - low-Cr group which could be restites (Wyman and Kerrich, 2009) or deep cumulates from tonalite- trondhjemite or Mg-rich boninitic arc magmas (Horodytskyi et al., 2007; Barth et al., 2002); A4 a group derived by crystallization of differentiated protokimberlite melts (Haggerty et al., 1979; Kamenetsky et al., 2009). The largest group B with Fe# (~ 0.15-0.25, moderate in Al and Na values, commonly reveal Eu anomalies. The GrB1 interpreted as subducted metagrabbro close to MORB (Jagoutz et al., 1974; Beard et al., 1996; Pearson, 1995; Snyder et al., 1997) reacted with oceanic water (Neal et al., 1990). Enriched Group B2 eclogites are thought to be products of fluid melting of ancient oceanic crust and interaction with peridotites during subduction (Aulbach et al., 2007). Group B3 eclogites (>3 GPa) may be basaltic cumulates derived from plume or ancient arc magmas in cratonic margins (Wyman and Kerrich, 2009); those near Moho may be eclogitized lower crustal cumulates (Shu et al., 2014). Group B4 eclogites are results of hybridization of subducted basalts with protokimberlite and other plume melts (Shatsky et al., 2008 -2015). High-Fe -Na Group C1 eclogites (Fe# > 0.27) may be subducted Fe- basalts; Ca-enriched varieties may be meta-tonalites or trondhjemites (Group C2) (Barth et al., 2002) and those which are very rich in Al could be metasediments (Group C3) (Mazzone and Haggerty, 1989). High -Ca- Al GrD1 are rare high-Ca and low-Fe varieties, commonly Al-rich and kyanite-bearing (sometimes with coesite) (grosspydites) which may be originally carbonate metasomatites (Smyth, 1977) or metapelites (Liou et al., 2014); Group GrD3 eclogites are high-Ca and moderate-Fe and may be ancient Mg-granites (Barth et al., 2002; Jacob et al., 2003) . According to the thermobarometry GrA eclogites are distributed mostly in the lower (L) and- middle parts of SCLM and correspond to low - temperature thermal gradients. GrB2 eclogites form trends of increasing Fe# for garnets and omphacites with decreasing pressure. This could be due to the progressive melting of subducted basalts (Rosenthal et al., 2014) or an opposite due to crystallization of evolving partial melts from primary eclogites. In USCLM the GrB3 omphacites show reactional trends with decreasing Fe# upward or an opposite progressive rise due to magmatic differentiation. GrC dominate the middle part of the SCLM (3-4 GPa) and mostly correspond to the layer originated in the Early Archean time at 3.5-4.0 GPa possibly due to subduction of the tonalitic crust and related metasediments. CrD1 -rich grosspyditic varieties from India, Siberia and South Africa are relatively low-Fe and Al-rich and possibly are metasomatites or products of interaction of sediments and peridotites. The other Ca- rich varieties most likely are subducted anorthosites or rare granites. Supported by the RFBR grants: 05-05-64718, 03-05-64146, 11 -05-00060, 11-05-91060-PICS, 16-05-00841, 16-05-00860 and projects 77-2, 65-03, 02-05 UIGGM SB RAS and ALROSA Stock Company
NASA Astrophysics Data System (ADS)
Gilio, Mattia; Clos, Frediano; Van Roermund, Herman L. M.
2013-04-01
The Scandinavian Caledonides (SC) are a deeply eroded Alpine-type orogenic belt formed by closure of the Iapetus ocean and collision between Baltica and Laurentia (500-380 Ma). The SC consists of a stack of Nappe Complexes (from bottom to top called Lower, Middle, Upper and Uppermost Allochthons) thrusted to the east over the Baltic Shield (Brueckner and Van Roermund, 2004; Gee et al., 2008). Fossil lithospheric mantle fragments, called orogenic peridotites, have been found within the (upper part of) middle, upper and uppermost Allochthons, as well as in the reworked basement gneisses (a.o Western Gneiss Complex (WGC)) along the Norwegian west coast. They occur as isolated lenses that contain diverse mineral parageneses and/or bulk rock compositions. Crustal incorporation of orogenic peridotite is classically interpreted to be the result of plate collisional processes related to orogeny (Brueckner and Medaris, 2000). The WGC and parts of the upper part of the Middle Allochthon (a.o. Seve Nappe Complex (SNC) in N Jämtland/S Västerbotten, central Sweden), are well known for the occurrence of high (HP) and ultrahigh pressure (UHP) metamorphic terranes (of Caledonian age). The (U)HPM evidence clearly demonstrates the deep metamorphic origin of these rocks interpreted to be caused by continental subduction and/or collision. Other metamorphic rocks (of Caledonian age) exposed in allochthonous nappes are solely characterised by greenschist-, amphibolite- and/or MP granulite "facies" mineral assemblages that can be interpreted, in the absence of retrogression, to have formed in less deeply subducted (and/or metamorphic) environments. This duality in metamorphic "facies" allows for a discrimination (at least theoretically) between "deep" versus "shallow" rooted nappes (in central parts of the Scandinavian Caledonides). Conform this reasoning, this duality should also be present within the Caledonian mineral assemblages (= metamorphic overprint) of orogenic peridotites (in central parts of the orogen), which, at least in the allochtonous nappes, have been interpreted to be "isofacial" with their host country rocks (Bucher, 1991). The latter strongly contrast to the interpretation of their "primary" (="protolith"- related) mineral assemblage(s) which clearly suggest a bimodal origin: here called thick (>80 km) versus thin (< 70 km) rooted lithospheric mantle protoliths. Distinction can be made on the basis of the presence of the stable (minimal Proterozoic) garnet-olivine assemblages in the protolith (i.e. much older than the Scandian collision event (Brueckner et al., 2010). For this reason orogenic garnet peridotite was first called "relict" garnet peridotite (Brueckner and Medaris, 2000), later rephrased into mantle wedge garnet peridotite (MWgp) by Van Roermund (2009). MWgp occurs in the WGC and in the SNC of the Upper Allochthon in central Sweden (Zhang et al., 2009). Most (All?) other protolith assemblages of orogenic peridotite in the CSC belong to the thin-rooted protolith subtype. No examples are known to us in which thin rooted prototypes became overprinted (during the Caledonian orogeny) by (U)HP metamorphic minerals, except for the subduction zone garnet peridotites (SZgp) in the WGC (Van Roermund, 2009). The latter can thus savely be interpreted as being enclosed within normal "MP" (or lower pressure) nappe sequences. As such it will be clear that this duality in protolith (and/or metamorphic) mineral assemblages of orogenic peridotite can be used to identify former, but now strongly retrogressed, (U)HP metamorphic terranes in other parts of the CSC (Gee et al, 2012). For this reason a comparative study has been made concerning field, (micro-)structural, mineral-chemical and/or geochemical aspects of two major orogenic peridotites from the SNC, central Sweden; here called the Friningen Garnet Peridotite (FGP) and the Kittelfjäll Spinel Peridotite (KSP), both exposed within the central belt of the SNC in central Sweden. The ultimate aim was to investigate whether the MWgp sub-type can be extended towards (Al-poor) spinel-bearing protolith assemblages or not. Results, including some hitherto unexpected mechanical effects, will be presented. References: Brueckner, H.K., Carswell, D.A., Griffin, W.L., Medaris, L.G., Van Roermund, H.L.M., Cuthbert, S.J. (2010). The mantle and crustal evolution of two garnet peridotite suites from the Western Gneiss Region, Norwegian Caledonides: An isotopic investigation. Lithos, 117, 1-19. doi:10.1016/j. Lithos.2010.01.011 Brueckner, H.K.and Medaris, L.G. (2000). A general model for the intrusion and evolution of "mantle" garnet peridotites in high-pressure and ultra-high-pressure metamorphic terranes. J. Metamorphic Geol., 18, 123-133. Brueckner H.K. and Van Roermund,H.L.M. (2004). Dunk tectonics: A multiple subduction//eduction model for the evolution of the Scandinavian Caledonides. Tectonics, 23, TC2004, doi:10.1029/2003tc001502. Bucher, K. (1991). Mantle fragments in the Scandinavian Caledonides. Tectonophysics, 190, 173-192. Gee, D.G., Fossen, H., Henriksen, N., Higgins, K. (2008). From the Early Paleozoic Platforms of Baltica and Laurentia to the Caledonide Orogen of Scandinavia and Greenland. Episodes, 31, 44-51. Gee, D.G., Janak, M., Majka, J., Robinson, P., Van Roermund, H.L.M (2012). UHP metamorphism along the Baltoscandian outer margin: evidence from the Seve Nappe Complex of the Swedish Caledonides. Lithosphere, in press. Janak, M., Van Roermund, H., Majka, J., Gee, D. (2012). UHP metamorphism recorded by kyanite-bearing eclogite in the Seve Nappe Complex of northern Jämtland, Swedish Caledonides. Gondwana Research, in press. Van Roermund, H.L.M. (2009). Mantle-wedge garnet peridotites from the northernmost ultra-high pressure domain of the Western Gneiss Region, SW Norway. Eur. J. Mineralogy, 21, 1085-1096. Zhang, C., Van Roermund, H.L.M., Zhang, L.F (2011). 16 - Orogenic Garnet Peridotites: Tools to Reconstruct Paleo-Geodynamic Settings of Fossil Continental Collision Zones. In: Ultrahigh Pressure Metamorphism, 25 Years After The Discovery Of Coesite And Diamond. London. Doi:10.1016/B978-0-12-385144-4.00015-1
A New Model of the Early Paleozoic Tectonics and Evolutionary History in the Northern Qinling, China
NASA Astrophysics Data System (ADS)
Dong, Yunpeng; Zhang, Guowei; Yang, Zhao; Qu, Hongjun; Liu, Xiaoming
2010-05-01
The Qinling Orogenic Belt extends from the Qinling Mountains in the west to the Dabie Mountains in the east. It lies between the North China and South China Blocks, and is bounded on the north by the Lushan fault and on the south by the Mianlue-Bashan-Xiangguang fault (Zhang et al., 2000). The Qinling Orogenic Belt itself is divided into the North and South Qinling Terranes by the Shangdan suture zone. Although the Shangdan zone is thought to represent the major suture separating the two blocks, there still exists debate about the timing and mechanism of convergence between these two blocks. For instance, some authors suggested an Early Paleozoic collision between the North China Block and South China Block (Ren et al., 1991; Kroner et al., 1993; Zhai et al., 1998). Others postulated left-lateral strike-slip faulting along the Shangdan suture at ca. 315 Ma and inferred a pre-Devonian collision between the two blocks (Mattauer et al., 1985; Xu et al., 1988). Geochemistry of fine-grained sediments in the Qinling Mountains was used to argue for a Silurian-Devonian collision (Gao et al., 1995). A Late Triassic collision has also been proposed (Sengor, 1985; Hsu et al., 1987; Wang et al., 1989), based on the formation of ultrahigh-pressure metamorphic rocks in the easternmost part of the Qinling Orogenic Belt at ~230 Ma (e.g., Li et al., 1993; Ames et al., 1996). Paleomagnetic data favor a Late Triassic-Middle Jurassic amalgamation of the North China and South China Blocks (Zhao and Coe, 1987; Enkin et al., 1992). It is clear that most authors thought that the Qinling Mountains are a collisional orogen, even they have different methods about the timing of the orogeny. Based on new detailed investigations, we propose a new model of the Early Paleozoic Tectonics and Evolutionary History between the North China and South China Blocks along the Shangdan Suture. The Shangdan suture is marked by a great number of ophiolites, island-arc volcanic rocks and other related rock assemblages. Our new geological and geochemical data revealed a lot of ophiolitic mélanges along the Shangdan suture, such as the Guojiagou, Ziyu, Xiaowangjian, Yanwan, Tangzang, Guanzizhen and Wushan areas from east to west. The ophiolite assemblage in Guojiagou, Ziyu area consists mainly of some blocks of E-MORB type and IAB-type basalts, while the pillow lavas from Xiaowangjian are IAB-type basalts. The basalts from the ophiolite assemblages in Yanwan, Tangzang and Wushan areas possess E-MORB geochemical compositions. The zircons of gabbro from Yanwan ophiolite mélange yield an U-Pb age of 516±3.8 Ma, which represents the formation age of the Yanwan ophiolite. Meanwhile, the basalts in the Guanzizhen ophiolite mélange show N-MORB type geochemical signature, and the zircons from gabbro yield a U-Pb age of 471±1.4 Ma, which constraints the formation age of the mature oceanic crust. Additionally, there also exists a U-Pb age of 523±26 Ma (Lu et al.,2003) and Cambrian-Ordovician radiolarites from the interlayed silicarites within the volcanic rock in the Guojiagou ophiolite mélange (Cui et al., 1995). All these geochemical and geochronological evidences indicate that there existed an oceanic basin and its subduction, which separated the Northern China Block from the Southern China Block during 523 -471 Ma. Accordant with this ocean and its subduction, there had been existed an active continental margin, island-arc setting on the north side of the Shangdan ophiolite mélange which were marked by a series of moderate-basic intrude igneous mass along the Sifangtai-Lajimiao area (Li et al., 1993) and the Fushui area (Dong et al., 1997). In addition to, there also exist a great number of subduction-collisional granites intruding into island-arc basement along the active continental margin. Zircons from the Fushui intrusion yield a U-Pb age of 514±1.3 Ma (Chen et al., 2004), which constraints the time of the subduction. Above all, more and more data suggest that there exists a back-arc basin on the northern side of the island-arc terrain. To the east, it is presented by the Erlangping group in Xixia area, which consists mainly of clastic sediments, carbonatites and basic volcanic rocks. The geochemistry of the basalts show that they were formed in a back-arc basin setting (Sun et al.,1996), and the radiolarites from the interlayed silicalites show the Orovician-Silurian age (Wang et al., 1995). Our new investigation reveals some new tectonic assemblages exposed in the Yinggerzui area, Qinghusi area to the west. The detailed geochemical studies indicate that they were formed in a back-arc basin. All above evidences suggest that there had existed an Early Paleozoic subduction system, which consists of a subduction trench, island-Arc and back-arc basin along the northern Qinling zone. It is also indicated that the Paleo-ocean had been evolved into a complete evolutionary process including initial spreading (E-MORB ophiolite), maturated extension (N-MORB ophiolite) and subduction (Island-arc volcanic rocks). However, it is notable that there are large scale of Devonian clastic sediments distributing on the south of the Shangdan suture, and the pre-Mesozoic rocks in the South Qinling without any metamorphism or just underwent the low-greenschist facies metamorphism in some places, which are very different from the North Qinling Terrane consisting mainly of Precambrian rocks and evolving into an amphibolite facies metamorphism at ~1.0 Ga and greenschist facies metamorphism at ~400 Ma (Liu et al., 1993; Zhang et al., 1994). Accordingly, it is prefer that there only occurred a subduction of the Shangdan oceanic crust from south to north along the Shangdan suture on the south of the Northern Qinling Terrane. However, the Piaochi and the Anjiping granites possessing the sym-collisional type granite geochemistry and formation age of 450-486 (Chen et al., 1991; zhang et al., 1996) indicate that there occurred a collisional event between the North Qinling Island-arc Terrane and the Northern China Block caused by closing of the Early Paleozoic back-arc basin. Additionally, the studies of the metamorphism show that there are two zones of high / ultra-high pressure metamorphic rocks outcropping along the both side of the Northern Qingling island-arc terrane. On the north, it is characterized by eclogite and coesite outcropping in the Guanpo area, and the metamorphic zircon U-Pb age of 507±38 Ma and 509±12 Ma by means of SHRIM (Yang et al., 2002). Meanwhile, there also exist some high pressure basic granulite (Liu et al., 1995) and felsic granulite (Liu et al., 1996) distributing in the Xigou fault on the south margin of the Northern Qingling island-arc terrane. Zircon U-Pb ages of 485±3.3 Ma by means of LA-ICP-MS method (Chen et al., 2004) and 518±12 Ma by means of SHRIM (Liu et al., 2003) constrain the time of the metamorphism. All these metamorphic data suggest the Northern Qingling island-arc terrane had been evolved into a deep subduction event during 485-518 Ma. Based on all above evidences, we infer a new model about the tectonics and evolutionary history of the Norhtern Qinling Terrane. It is emphasized that the Early Paleozoic tectonics between the North China and Southern China Blocks had existed an ocean, island-arc and back-arc basin, and evolved into four stages of evolutionary stages: 1) initial spreading along the Shangdan zone during 516-523 Ma; 2) maturated ocean along the Shangdan zone during 516-471 Ma; 3) subduction along the south side of the Northern Qinling Terrane and formation of the Back-arc basin along the north side of the Northern Qinling Terrane during518-514; 4) closing of the back-arc basin, collision between the Northern Qingling island-arc terrane and the Northern China Block, and deep subduction of the Northern Qingling island-arc terrane during 518-485Ma. This work was supported by NSFC (40772140 & 40972140)