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1.
van Roermund  & Drury 《地学学报》1998,10(6):295-301
We report here for the first time the occurrence of relics of majoritic garnet within orogenic garnet peridotites from Otrøy, Western Gneiss Region, Norway. The microstructural evidence consists of two-pyroxene exsolution from garnet. Majoritic garnets are only stable at depths greater than 150 km. Estimates of the initial composition of the majoritic garnets imply pressures of 6–6.5 GPa indicating that the Otrøy peridotites were derived from depths > 185 km.
  Mineral-chemical data indicate that the present mineral compositions equilibrated at mantle conditions around 805 ± 40 °C and 3.2 ± 0.2 GPa.
  Estimates of the initial pressure temperature (PT) conditions and PTtime ( t ) path are consistent with a multistage, multiorogenic exhumation history with upwelling of hot asthenosphere up to ≈ 100 km in the Pre-Cambrian followed by subsequent crustal emplacement and exhumation during the Caledonian orogeny.  相似文献   

2.
High-temperature peridotite massifs occur as lensoid bodies with high-pressure granulites in the southern Bohemian massif. In lower Austria the peridotites comprise garnet lherzolites lacking primary spinel, rare garnet and garnet-spinel harzburgites, and harzburgites containing Cr-rich primary spinel instead of garnet. These phase assemblages suggest initial high-pressure equilibration and are consistent with results from garnet-orthopyroxene geobarometry indicating equilibration at around 3–3.5 GPa. Maximum temperature estimates obtained on core compositions of coexisting minerals from the peridotites are not higher than ca. 1100 °C. In contrast, pyroxene megacryst compositions, garnet exsolution textures in the garnet pyroxenites, and results from geothermometry indicate much higher original equilibration temperatures in most of the pyroxenites (up to 1400 °C). High temperatures, modal zoning, the occasional presence of Mg-rich garnetites and chemical evidence suggest that the pyroxenites are cumulates which crystallized from low-degree melts derived from the sub-lithospheric mantle. Isothermal interpolation of the high temperatures to an upper mantle adiabat suggests that the melts were derived from a minimum depth of 180–200 km. The formation of small garnet II grains and garnet exsolution lamellae in the pyroxenites and pyroxene megacrysts may reflect isobaric cooling of the cumulates from temperatures above 1400 °C to ca. 1100–1200 °C (at 3–3.5 GPa) to approach the ambient lithospheric isotherm. This model differs from other models in which the formation of garnet II was explained by an increase in pressure during cooling in a subduction zone. Isobaric cooling was followed by near-isothermal decompression from 3–3.5 GPa to 1.5–2 GPa at 1000–1200 °C, as indicated by the increase of Al in pyroxenes near garnet. Further cooling in the spinel lherzolite stability field is indicated by spinel exsolution lamellae in pyroxenes from lherzolites. The formation of symplectites and kelyphites indicate sub-millimetre scale re-equilibration during exhumation in the course of the Carboniferous collision in the Bohemian massif. The peridotite massifs represent fragments of normal (non-cratonic) lithospheric mantle from a Paleozoic convergent plate margin. Received: 22 July 1996 / Accepted 28 February 1997  相似文献   

3.
Garnet peridotites from the southern Su‐Lu ultra‐high‐pressure metamorphic (UHPM) terrane, eastern China, contain porphyroblastic garnet with aligned inclusions comprising a low‐P–T mineral assemblage (chlorite, hornblende, Na‐gedrite, Na‐phlogopite, talc, spinel and pyrite). Orthopyroxene porphyroblasts show fine exsolution lamellae of clinopyroxene and minor chromite. A clinopyroxene inclusion in garnet shows some orthopyroxene exsolution lamellae. Both the rims of porphyroblastic pyroxene and garnet and the matrix pyroxene and garnet crystallized at the expense of olivine. This is interpreted as a result of metasomatism of the peridotites by an SiO2‐rich melt at UHP conditions. A chromian garnet further overgrew on the rims of the garnet. The XMg values (Mg/(Mg+Fe)) of porphyroblastic garnet decrease from core to rim and vary in different peridotite samples, while the compositions of both the porphyroblastic and the matrix pyroxene are similar in terms of Ca–Mg–Fe. The Mg‐rich cores of porphyroblastic garnet and orthopyroxene record high temperatures and pressures (c. 1000 °C, ≥5.1 GPa), whereas the matrix minerals, including the rims of porphyroblasts, record much lower P–T (c. 4.2 GPa, c. 760 °C). Sm–Nd data give apparent isochron ages of c. 380 Ma and negative εNd(0) values (c.?9). These dates are considered meaningless due to isotopic disequilibrium between garnet cores and the rest of the rocks. The isotopic disequilibrium was probably caused by metasomatism of the peridotites by melt/fluids derived from the coevally subducted crustal materials. On the other hand, the Rb–Sr isotopic systems of phlogopite and clinopyroxene appear to have reached equilibrium and record a cooling age of c. 205 Ma. It is suggested that the garnet peridotites were originally emplaced into a low‐P–T environment prior to the c. 220 Ma continental collision, during which they were subducted together with crustal rocks to mantle depth and subjected to UHP metamorphism. An important corollary is that at least some of the coevally subducted crustal rocks in the Su‐Lu terrane have been subjected to peak metamorphism at P–T conditions much higher than presently estimated (≥2.7 GPa, ≤800 °C).  相似文献   

4.
Observations of oriented SiO2 precipitates in omphacite from eclogite with tholeiitic basalt protolith bordering the Alpe Arami garnet peridotite massif, Ticino, Switzerland, and petrological studies of the eclogitic mineral assemblages, suggest that this rock was subjected to higher‐pressure metamorphism than previously realized. We employed various calibrations of the Fe2+ ? Mg exchange thermometer and calculations of equilibria with thermodynamic data, considering the calcium–Tschermak's component (CaAl2SiO6), of garnet‐pyroxene pairs. From these calculations, it is concluded that the eclogitic lenses have recorded at least four stages of mineral growth corresponding to the following: Stage I (prograde) c. 2.4 GPa; 700 °C; Stage IIa (maximum recorded grade) c. 7.0 GPa; 1100 °C; Stage IIb (retrograde) c. 3.7 GPa; 900 °C; Stage III (retrograde) c. 2.1 GPa; 750 °C. Because of the preservation of Stage I, a relatively rapid subduction and exhumation of Alpe Arami eclogite is suggested. The exhumation path of the eclogitic rock is in good agreement with most exhumation paths inferred for the Alpe Arami garnet lherzolite proposed previously by several authors based upon a variety of different observations, although the eclogite and peridotite exhumation paths may diverge at depths greater than 120 km.  相似文献   

5.
Eclogite facies metarodingites occur as deformed dykes in serpentinites of the Zermatt‐Saas ophiolite (Western Alps). They formed during the subduction of the Tethys oceanic lithosphere in the Early Tertiary. The metarodingites developed as a consequence of serpentinization of the oceanic mantle. Three major types of metarodingites (R1, R2 & R3) can be distinguished on the basis of their mineralogical composition. All metarodingites contain vesuvianite, chlorite and hydrogrossular in high modal amounts. In addition they contain: R1 – diopside, tremolite, clinozoisite, calcite; R2 – hydroandradite, diopside, epidote, calcite; and R3 – hydroandradite. Both garnets contain a small but persistent amount of hydrogarnet component. The different metarodingites reflect different original dyke rocks in the mantle. In each group of metarodingite, textural relations suggest that reactions adjusted the assemblages along the P–T path travelled by the ophiolite during subduction and exhumation. Reactions and phase relations derived from local textures in metarodingite can be modelled in the eight‐component system: SiO2‐Al2O3‐Fe2O3‐FeO‐MgO‐CaO‐CO2‐H2O. This permits the analysis of redox reactions in the presence of andradite garnet and epidote in many of the rocks. Within this system, the phase relations in eclogite facies metarodingites have been explored in terms of T–XCO2, T–μ(SiO2), μ(Cal)–μ(SiO2) and P–T sections. It was found that rodingite assemblages are characterized by low μ(SiO2) and low XCO2 conditions. The low SiO2 potential is externally imposed onto the rodingites by the large volume of antigorite‐forsterite serpentinites enclosing them. Moreover, μ(SiO2) decreases consistently from metarodingite R1 to R3. The low μ(SiO2) enforced by the serpentinites favours the formation of hydrogarnet and vesuvianite. Rodingite formation is commonly associated with hydrothermal alteration of oceanic lithosphere at the ocean floor, in particular to ocean floor serpentinization. Our analysis, however, suggests that the metarodingite assemblages may have formed at high‐pressure conditions in the subduction zone as a result of serpentinization of oceanic mantle by subduction zone fluids.  相似文献   

6.
We report here the detailed microstructure and chemistry of pyroxene exsolution from a polycrystalline garnet porphyroblast of the Western Gneiss Region (WGR) garnet peridotite, Otrøy, Norway. For both clinopyroxene (Cpx) and orthopyroxene (Opx), the same basic crystallographic relationship is found with the host garnet: (100)py//{112}grt, (010)px//{110}grt and (001)px//{111}grt for the majority (>90%) of its intracrystalline pyroxene rods. In addition, this pattern is also exhibited by some interstitial Opx and a subpopulation of both pyroxenes shows a different pattern or no discernible pattern. The results provide quantitative microstructural evidence demonstrating an exsolution (precipitation) origin of both the intracrystalline Cpx and Opx and the small interstitial Opx crystals. The reconstructed precursor majoritic garnet, taking into account both the intracrystalline pyroxenes and interstitial Opx, was characterized by Si = ～3.07 cation per formula unit that corresponds to a minimum pressure of 7.7 GPa (～250 km depth). We also deduce from the observation of Opx being the majority of intracrystalline precipitates and 100% of the interstitial ones that the precursor majoritic garnet probably originated from a pressure less than ～10 GPa (～300 km depth). A multistage decomposition hypothesis is proposed for this WGR majoritic garnet during exhumation of the peridotite from 250 to 300 km depth to explain the topotaxy and chemistry of the exsolved pyroxenes.  相似文献   

7.
The Jiangzhuang ultrahigh‐pressure (UHP) metamorphic peridotite from south Sulu, eastern China occurs as a layer within gneiss with eclogite blocks, and consists of coarse‐grained garnet porphyroblasts and a fine‐grained matrix assemblage of garnet + forsterite + enstatite + diopside ± phlogopite ± Ti‐clinohumite ± magnesite. Both types of garnet are characterized by high MgO content and depletion of light rare earth element (LREE) and enrichment of heavy rare earth element, but the matrix garnet has lower MgO, TiO2 and higher Cr2O3 and REE contents. Diopside displays LREE enrichment, and has low but variable large‐ion lithophile element (LILE) contents. Phlogopite is a major carrier of LILE. Ti‐clinohumite contains high Nb, Ta, Cr, Ni, V and Co contents. The P–T conditions of 4.5–6.0 GPa and 850–950 °C were estimated for matrix mineral assemblages. Most peridotites are depleted in Al2O3, CaO and TiO2, and enriched in SiO2, K2O, REE and LILE. In contrast to phlogopite‐free peridotites, the phlogopite‐bearing peridotites have higher K2O, Zr, REE and LILE contents. Zircon occurs only in the phlogopite‐bearing peridotites, shows no zoning, with low REE contents and Th/U ratios, and yields tight U–Pb ages of 225–220 Ma, indicating the peridotites experienced consistent Triassic UHP metamorphism with subducted supercrustal rocks. These data demonstrate that the Jiangzhuang peridotites were derived from the depleted mantle wedge of the North China Craton, and experienced various degrees of metasomatism. The phlogopite‐free peridotites may have been subjected to an early cryptic metasomatism at UHP conditions of the mantle wedge, whereas the phlogopite‐bearing peridotites were subjected to a subsequent strong metasomatism, characterized by distinctly enrichment in LILE, LREE, Zr and K as well as the growth of zircon and volatile‐bearing minerals at UHP subduction conditions. The related metasomatism may have resulted from the filtration of fluids sourced mainly from deeply subducted supracrustal rocks.  相似文献   

8.
Garnet peridotites occur in quartzofeldspathic gneisses in the Northern Qaidam Mountains, western China. They are rich in Mg and Cr, with mineral compositions similar to those in mantle peridotites found in other orogenic belts and as xenoliths in kimberlite. Garnet‐bearing lherzolites interlayered with dunite display oriented ilmenite and chromite lamellae in olivine and pyroxene lamellae in garnet that have been interpreted to indicate pressures in excess of 6 GPa. However, some garnet porphyroblasts include hornblende, chlorite and spinel + orthopyroxene symplectite after garnet; some clinopyroxene porphyroblasts include abundant actinolite/edenite, calcite and lizardite in the lherzolite; some olivine porphyroblasts (Fo92) include an earlier generation Mg‐rich olivine (Fo95–99), F‐rich clinohumite, pyroxene, chromite, anthophyllite/cummingtonite, Cl‐rich lizardite, carbonates and a new type of brittle mica, here termed ‘Ca‐phlogopite’, in the associated dunite. The pyrope content of garnet increases from core to rim, reaching the pyrope content (72 mol.%) of garnet typically found in the xenoliths in kimberlite. The simplest interpretation of these observations is that the rock association was formerly mantle peridotite emplaced into the oceanic crust that was subjected to serpentinization by seawater‐derived fluids near the sea floor. Dehydration during subduction to 3.0–3.5 GPa and 700 °C transformed these serpentinites into garnet lherzolite and dunite, depending on their Al and Ca contents. Pseudosection modelling using thermocalc shows that dehydration of the serpentinites is progressive, and involved three stages for Al‐rich and two stages for Al‐poor serpentinites, corresponding to the breakdown of the key hydrous minerals. Static burial and exhumation make olivine a pressure vessel for the pre‐subduction mineral inclusions during ultrahigh‐pressure (UHP) metamorphism. The time span of the UHP event is constrained by the clear interface between the two generations of olivine to be very short, implying rapid subduction and exhumation.  相似文献   

9.
The enthalpies of solution of petrologically important phases in the system MgO-Al2O3-SiO 2 were measured in a melt of composition 2PbO · B2O3 at 970 ± 2K. The substances investigated included synthetic and natural (meteoritic) enstatite (MgSiO3), synthetic aluminous enstatite (MgSiO30.9Al2O30.1), synthetic and natural cordierite (Mg2Al4Si5O18), synthetic and natural sapphirine (approx. 7MgO·9Al2O3 · 3SiO2), synthetic spinel (MgAl2O4), natural sillimanite (Al2SiO5), synthetic forsterite (Mg2SiO4), synthetic pyrope (Mg3Al2Si3O12), natural quartz (SiO2), synthetic periclase (MgO) and corundum (Al2O3). Improvement in standardization of the calorimeter solvent made possible greater precision in this study than obtainable in former work in this laboratory on some of the same substances.The enthalpies of formation of enstatite, synthetic cordierite, forsterite and spinel are in reasonable agreement with values previously determined by solution calorimetry. The enthalpy of formation of enstatite is about 0.7 kcal less negative than the value for clinoenstatite resulting from the HF calorimetry of Torgesen and Sahama (J. Amer. Chem. Soc.70. 2156–2160, 1948), and is in accord with predictions based on analysis of published pyroxene equilibrium work. Aluminous enstatite with 10 wt.% Al2O3 shows an enthalpy of solution markedly lower than pure MgSiO3: the measurements lead to an estimate of the enthalpy of formation at 970 K for MgAl2SiO6 (Mg-Tschermak) orthopyroxene of + 9.4 ± 1.5 kcal/mole from MgSiO3 and Al2O3.Comparison of the enthalpies of formation of synthetic cordierite and anhydrous natural low-iron cordierite shows that they are energetically quite similar and that the synthetic cordierite is not likely to have large amounts of (Al, Si) tetrahedral disorder. Comparison of the enthalpies of formation of synthetic sapphirine and natural low-iron sapphirine shows, on the other hand, that the former is not a good stability model for the latter. The lower enthalpy of formation of the high-temperature synthetic sample is undoubtedly a consequence of cation disordering.The enthalpy of formation of natural sillimanite is considerably less negative than given by the tables of Robie andWaldbaum (U.S. Geol. Surv. Bull.1259 1968).The measured enthalpy of formation of synthetic pyrope is consistent with that deduced from published equilibrium diagrams in conjunction with the present measured enthalpy of formation of aluminous enstatite. Calculation of the entropy of synthetic pyrope from the present data yields surprisingly high values and suggests that synthetic pyrope is not a good stability model for natural pyrope-rich garnets. Hence, considerable doubt exists about the direct quantitative application of experimental diagrams involving pyropic garnet to discussions of the garnet stability field in the Earth's outer regions.  相似文献   

10.
We report the field, petrographic and mineral chemical characteristics of relict super‐silicic (=majoritic) garnet microstructures from the Otrøy peridotites in the Western Gneiss Region, Norway. The evidence for the former existence of super‐silicic garnet consists of two‐pyroxene exsolution microstructures from garnet. Estimates of the initial composition of the super‐silicic garnet imply pressures of 6–6.5 GPa, indicating that the Otrøy garnet peridotites were derived from depths >185 km. The garnet peridotites consist of inter‐banded variable compositions with c. 50% garnet peridotite and 50% garnet‐free peridotite. Two distinct garnet types were identified: (a) normal matrix garnet, grain‐size ≤4 mm, and (b) large isolated single garnet crystals and/or (polycrystalline) garnet nodules up to 10 cm in size. Large garnet nodules occur only within limited bands within the garnet peridotites. The relicts of super‐silicic garnet were exclusively found in some (not all) of the larger garnet nodules. Petrographic observations revealed that the microstructure of nodular garnet consists of the following four characteristic elements. (1) Individual garnet nodules are polycrystalline, with grain sizes of 2–8 mm. Garnet grain boundaries are straight with well‐defined triple junctions. (2) Some garnet triple junctions and garnet grain boundaries are decorated by interstitial orthopyroxene. (3) Cores of larger polycrystalline garnet contain two‐pyroxene exsolution microstructures. (4) Precipitation‐free rims (2 mm thick) surround garnet cores containing the exsolved pyroxene microstructure. Pyroxene exsolution from super‐silicic garnet was subsequently followed by brittle–ductile deformation of garnet. Both exsolved pyroxene needles and laths become undulous or truncated by fractures. Simultaneous garnet plasticity is indicated by the occurrence of high densities of naturally decorated dislocations. Transmission electron microscopy observations indicate that decoration is due to Ti‐oxide precipitation. Estimates of the P–T conditions for mineral chemical equilibration were obtained from geothermobarometry. The mineral compositions equilibrated at mantle conditions around 805±40 °C and 3.2±0.2 GPa. These P–T estimates correspond to cold continental lithosphere conditions at depths of around 105 km. From a combination of both depth estimates it can be concluded that the microstructural memory of the rock extends backwards to twice as great a depth range as obtained by thermobarometric methods. Available geochronological and geochemical data of Norwegian garnet peridotites suggest a multi‐stage, multi‐orogenic exhumation history.  相似文献   

11.
Mixtures of synthetic crystalline enstatite and diopside were reacted with small water contents in sealed capsules in piston-cylinder apparatus at 30 kb between 1000° C and 1700° C. The compositions of coexisting enstatite and diopside solid solutions were measured with an ARL-EMX electron microprobe between 1000° C and 1500° C. Between 1100° C and 1500° C the pyroxenes coexisted with H2O-undersaturated liquid which quenched to inhomogeneous pyroxene crystals. The presence of liquid facilitated growth of pyroxene crystals suitable for microprobe determinations. The solvus of Davis and Boyd (1966) is generally used in geothermometry; our enstatite solvus limb is a few mol-% richer in Mg2Si2O6 in the temperature range 1000–1400° C; our diopside solvus limb is a few mol-% richer in Mg2Si2O6 below 1100°C, in close agreement between 1100° C and 1200° C, but richer in CaMgSi2O6 between 1200° C and 1500° C. Estimated equilibration temperatures for a diopside with composition 78.7% Di is 1300° C according to our results compared with 1210° C for the Davis and Boyd solvus.  相似文献   

12.
Summary Mineralogical characteristics of eclogite xenoliths from three kimberlite pipes (KL2, P2 and P10) of the Proterozoic Wajrakarur kimberlite field of southern India have been studied. In a rare sample of enstatite eclogite from the KL2 pipe garnet contains microscopic triangular arrays of needles or blebs of omphacite, enstatite and rutile consistent with an origin by exsolution parallel to the isometric form {111}. Discrete omphacite grains in the sample contain exsolved needles or blebs of enstatite and garnet. Kyanite eclogites are abundant in the KL2 pipe which occasionally show a secondary ring of pure celsian around kyanite grains. Omphacite Na2O contents in the eclogites of the KL2 and P2 pipes are typically between 3 and 6 wt%, and garnet has widely variable composition with end member ranges of Prp22-81Grs0-47Alm10-30Sps0-1Adr0-5Uv0-3. Eclogites of the P10 pipe comprise chromian omphacite and garnet. Phase relations in the ACF projection exhibit systematic increase of the Ca-Tschermak’s component in omphacite from enstatite eclogite through biminerallic eclogite to kyanite eclogite. Garnet-clinopyroxene Fe–Mg geothermometry yields temperatures mostly in the range of 900–1100 °C. A formerly supersilicic nature of garnet in enstatite eclogite as inferred from exsolution mineralogy indicates minimum peak pressure of 5 GPa.  相似文献   

13.
Peridotite xenoliths containing primary phlogopite with or without potassic richterites as major constituent (up to 12 vol. %) are rarely found in kimberlite from the Bultfontein Floors. Chemically, these rocks are similar in compositions with those of the granular type garnet peridotite xenoliths from South Africa and Lesotho, except for an abnormally high content of K2O in the former. Phlogopite and potassic richterite are thought to have the following genesis: garnet peridotites at a depth from 170 to 100 km suffered local introduction of a potash-rich fluid, and garnet and enstatite reacted with this fluid to form phlogopite and diopside. Potassic richterite may have been produced by the reaction between diopside and fluid at the same time as crystallization of phlogopite at depths shallower than 120 km.  相似文献   

14.
The CCSD‐PP1 drillhole penetrated a 110‐m‐thick sequence of the Zhimafang ultramafic body in the Sulu ultrahigh‐pressure (UHP) metamorphic belt, east China. The sequence consists of interlayered garnet‐bearing (Grt) and garnet‐free (GF) peridotite. Eleven layers of Grt‐peridotite, ranging from 1.2 to 9.5 m in thickness, have an aggregate thickness of 54.49 m, whereas eight layers of GF‐peridotite, ranging from 2.2 to 14.2 m in thickness, have a total thickness of 57.53 m. The boundaries between the two rock types are gradational. The Grt‐peridotites have slightly higher contents of Al2O3, CaO and SiO2, and lower Mg#s (0.90–0.92) than the GF‐peridotites (Mg#s 0.91–0.93). Both contain low TiO2 (<0.05 wt%) and have higher modal abundances of enstatite (average 10 vol.%) than diopside (1–5 vol.%), typical of depleted‐type upper mantle. The diopside in these rocks has high and relatively uniform Mg# members (0.93–0.95), but highly variable Al2O3 (0.2–2.3 wt%), Na2O (0.5–2.5 wt%) and Cr2O3 (0.38–2.09 wt%). Enstatite (En92?93) contains very low Al2O3 (0–0.3 wt%). Both porphyroblastic and equigranular garnet are present. The equigranular varieties are zoned, from core to rim in Cr2O3 (3.4–4.2 wt%), MgO (18.4–17.5 wt%) and Al2O3 (21.1–20.1 wt%). Titania is very low in all the garnet, mostly <0.05 wt%. Chromite or chromium (Cr)‐spinel occur both in the Grt‐ and GF‐peridotite, and are characterized by high contents of Cr2O3 (49–58 wt%) and FeO (24–43 wt%), similar to that in iron‐rich Alpine‐type peridotites. Based on the bulk‐rock MgO–FeO compositions, the Zhimafang Grt‐peridotite probably underwent 20–30% partial melting, whereas the GF‐peridotite may have undergone as much as 35–40% partial melting, suggesting that the two rock types owe their differences to different degrees of partial melting rather than to pressure differences during metamorphism.  相似文献   

15.
Diffusion modelling of growth-zoned garnet is used in combination with standard geothermometric and geobarometric techniques to estimate cooling and denudation rates from the mafic eclogites of the Red Cliff area, Great Caucasus, Russia. Euhedral garnet porphyroblasts exhibit different degrees of prograde growth zoning depending on the size of the grain (100 μm to several mm in diameter). Zoning patterns are mainly expressed in terms of Fe–Mg exchange, with 100*Mg/(Mg+Fe) increasing from 18–20 to 33–37 from core to rim. Geothermobarometry yields conditions of 680±40 °C and a minimum of 1.6±0.2 GPa and of 660±40 °C and 0.8±0.2 GPa for the high-pressure and retrograde stages of equilibration, respectively. A temperature of 600±40 °C has been recorded for the late-stage metamorphic overprint in the mica schists surrounding the eclogites. Relaxation of garnet zoning profiles was modelled for three different hypothetical P–T –t trajectories, all with an initial temperature of 680 °C and a pressure change of 0.8 GPa. The first two trajectories involve decompression associated with regular cooling down to 660 °C (near isothermal) and 600 °C. The third path is a two-step trajectory comprising near-isobaric cooling down to 600 °C followed by isothermal decompression to 0.8 GPa. These P–T trajectories cover as wide a range of pressure and temperature changes endured by the rocks as possible, thus representing extreme cases for calculating cooling and exhumation rates. Calculations indicate that the zoning pattern of the smallest garnet (i.e. garnet for which the zoning is most easily eliminated during post-growth processes) along the different paths can be preserved for the following average exhumation and cooling rates: path 1, 143 mm a?1 and 102 °C Ma?1; path 2, 60 mm a?1 and 171 °C Ma?1; path 3, 11–30 mm a?1 and 200–400 °C Ma?1. These results are discussed in light of theoretical P–T–t paths extracted from thermal models of regions of thickened crust, and from analogue models of accretionary wedge and continental lithosphere subduction.  相似文献   

16.
Exsolution lamellae of garnet in clinopyroxene and orthopyroxene porphyroclasts from garnet pyroxenites in the Moldanubian zone were studied to elucidate the pressure–temperature conditions of the exsolution process and to reconstruct the burial and exhumation path of ultramafic rocks in the Variscan orogen. The porphyroclasts occur in a fine-grained matrix with metamorphic fabrics, which consists of clinopyroxene and small amounts of garnet, orthopyroxene and amphibole. The clinopyroxene porphyroclasts contain garnet + orthopyroxene lamellae as well as ilmenite rods that have orientation parallel to (100) planes of the porphyroclasts. Orthopyroxene porphyroclasts host garnet and clinopyroxene lamellae, which show the same lattice preferred orientation. In both cases, lamellar orthopyroxene, clinopyroxene and garnet were partially replaced by secondary amphibole. Composition of exsolution phases and that of host pyroxene were reintegrated according to measured modal proportions and demonstrate that the primary pyroxene was enriched in Al and contained 8–11 mol.% Tschermak components. Conventional thermobarometry and thermodynamic modelling on the reintegrated pyroxene indicate that primary clinopyroxene and orthopyroxene megacrysts crystallized at 1300–1400 °C and 2.2–2.5 GPa. Unmixing and exsolution of garnet and a second pyroxene phase occurred in response to cooling and pressure increase before the peak pressure of 4.5–5.0 GPa was reached at ∼1100 °C. This scenario is consistent with a burial of hot upper-mantle ultramafics into a cold subcratonic environment and subsequent exhumation through 900 °C and 2.2–3.3 GPa, when the pyroxenites would have partially recrystallized during tectonic incorporation into eclogites and felsic granulites.  相似文献   

17.
J.B. Dawson   《Lithos》2004,77(1-4):553-569
Porphyroclastic enstatite in a garnet lherzolite xenolith from the Monastery Mine kimberlite, South Africa, has exsolved pyrope garnet, Cr-diopside and Al-chromite, and the specimen is interpreted as representing a transition from fertile harzburgite, (containing high Ca-Al-Cr enstatite) to granular garnet lherzolite. Although the exsolved phases occur in morphologically different forms (fine and coarse lamellae; equant, ripened grains), indicating textural disequilibrium, the exsolved grains are very constant in composition, indicating chemical equilibrium. Theoretically, the exsolution could have been due to a fall in temperature, but the close association of exsolution and deformation of the host enstatite suggests that exsolution was also aided by straining of the enstatite lattice. The phase compositions can be broadly matched with those in other mantle peridotites, except that all phases are characterised by a virtual absence of Ti. In the garnet and diopside Ti, Co, Zr and most of the REE are lower than in published analyses of garnet and diopside in both granular and sheared garnet lherzolites from Southern African kimberlites, and diopside/garnet partitioning for Sr and the REE is higher. Comparison with the trace element chemistry of an enstatite from a fertile harzburgite indicates that, except for Nb, the trace element content and distribution found in the Monastery phases could arise by isochemical exsolution from such an enstatite. On the assumption that (a) the Monastery specimen represents a transition from harzburgite to garnet lherzolite, and (b) many garnet lherzolites are of exsolution origin (as suggested by their modal compositions), the inference is that most garnet lherzolites, and not just the sheared variety, have been subject to varying degrees of Ti, Zr, Sr and REE metasomatism.  相似文献   

18.
The Xugou garnet peridotite body of the southern Sulu ultrahigh‐pressure (UHP) terrane is enclosed in felsic gneiss, bounded by faults, and consists of harzburgite and lenses of garnet clinopyroxenite and eclogite. The peridotite is composed of variable amounts of olivine (Fo91), enstatite (En92?93), garnet (Alm20?23Prp53?58Knr6?9Grs12?18), diopside and rare chromite. The ultramafic protolith has a depleted residual mantle composition, indicated by a high‐Mg number, very low CaO, Al2O3 and total REE contents compared to primary mantle and other Sulu peridotites. Most garnet (Prp44?58) clinopyroxenites are foliated. Except for rare kyanite‐bearing eclogitic bands, most eclogites contain a simple assemblage of garnet (Alm29?34Prp32?50Grs15?39) + omphacite (Jd24?36) + minor rutile. Clinopyroxenite and eclogite exhibit LREE‐depleted and LREE‐enriched patterns, respectively, but both have flat HREE patterns. Normalized La, Sm and Yb contents indicate that both eclogite and garnet clinopyroxenite formed by high‐pressure crystal accumulation (+ variable trapped melt) from melts resulting from two‐stage partial melting of a mantle source. Recrystallized textures and P–T estimates of 780–870 °C, 5–7 GPa and a metamorphic age of 231 ± 11 Ma indicate that both mafic and ultramafic protoliths experienced Triassic UHP metamorphism in the P–T forbidden zone with an extremely low thermal gradient (< 5 °C km?1), and multistage retrograde recrystallization during exhumation. Develop of prehnite veins in clinopyroxenite, eclogite, felsic blocks and country rock gneiss, and replacements of eclogitic minerals by prehnite, albite, white mica, and K‐feldspar indicate low‐temperature metasomatism.  相似文献   

19.
Enthalpies of solution of synthetic clinopyroxenes on the join CaMgSi2O6-Mg2Si2O6 have been measured in a melt of composition Pb2B2O5 at 970 K. Most of the measurements were made on samples crystallized at 1600°–1700°C and 30 kbar pressure, which covered the range 0–78 mole per cent Mg2Si2O6, and whose X-ray patterns could be satisfactorily indexed on the diopside (C2/c) structure. For the reaction: Mg2Si2O6→-Mg2Si2O6 enstatite diopside the present data, in conjunction with previous and new measurements on Mg2Si2O6 enstatite, determine ΔH° ~ 2 kcal and WH (regular solution parameter) ~ 7 kcal. These values are in good agreement with those deduced by Saxena and Nehru (1975) from a study of high temperature, high pressure phase equilibrium data under the assumption that the excess entropy of mixing is small, but, in light of the recent theoretical treatment of Navrotsky and Loucks (1977, Phys. Chem. Min.1, 109–127), the meanings of these parameters may be ambiguous.Heat of solution measurements on Ca-rich binary diopsides made by annealing glasses at 1358°C in air gave slighter higher values than the higher temperature high pressure samples. This may be evidence for some (Ca, Mg) disorder of the sort postulated by Navrotsky and Loucks (1977, Phys. Chem. Min.1, 109–127), although no differences in heat of solution dependent on synthesis temperature in the range 1350°–1700°C could be found in stoichiometric CaMgSi2O6.  相似文献   

20.
Garnet-bearing mantle peridotites, occurring as either xenoliths in volcanic rocks or lenses/massifs in high-pressure and ultrahigh-pressure terrenes within orogens, preserve a record of deep lithospheric mantle processes. The garnet peridotite xenoliths record chemical equilibrium conditions of garnet-bearing mineral assemblage at temperatures (T) ranging from ~700 to 1,400°C and pressures (P) > 1.6–8.9 GPa, corresponding to depths of ~52–270 km. A characteristic mineral paragenesis includes Cr-bearing pyropic garnet (64–86 mol% pyrope; 0–10 wt% Cr2O3), Cr-rich diopside (0.5–3.5 wt% Cr2O3), Al-poor orthopyroxene (0–5 wt% Al2O3), high-Cr spinel (Cr/(Cr + Al) × 100 atomic ratio = 2–86) and olivine (88–94 mol% forsterite). In some cases, partial melting, re-equilibration involving garnet-breakdown, deformation, and mantle metasomatism by kimberlitic and/or carbonatitic melt percolations are documented. Isotope model ages of Archean and Proterozoic are ubiquitous, but Phanerozoic model ages are less common. In contrast, the orogenic peridotites were subjected to ultrahigh-pressure (UHP) metamorphism at temperature ranging from ~700 to 950°C and pressure >3.5–5.0 GPa, corresponding to depths of >110–150 km. The petrologic comparisons between 231 garnet peridotite xenoliths and 198 orogenic garnet peridotites revealed that (1) bulk-rock REE (rare earth element) concentrations in xenoliths are relatively high, (2) clinopyroxene and garnet in orogenic garnet peridotites show a highly fractionated REE pattern and Ce-negative anomaly, respectively, (3) Fo contents of olivines for off-cratonic xenolith are in turn lower than those of orogenic garnet and cratonic xenolith but mg-number of garnet for orogenic is less than that of off-cratonic and on-cratonic xenolith, (4) Al2O3, Cr2O3, CaO and Cr# of pyroxenes and chemical compositions of whole rocks are very different between these garnet peridotites, (5) orogenic garnet peridotites are characterized by low T and high P, off-cratonic by high T and low P, and cratonic by medium T and high P and (6) garnet peridotite xenoliths are of Archean or Proterozoic origin, whereas most of orogenic garnet peridotites are of Phanerozoic origin. Taking account of tectonic settings, a new orogenic garnet peridotite exhumation model, crust-mantle material mixing process, is proposed. The composition of lithospheric mantle is additionally constrained by comparisons and compiling of the off-cratonic, on-cratonic and orogenic garnet peridotite.  相似文献   

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