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1.
Extraordinarily high Pb content in K-feldspar and plagioclase has been found contiguous to monazite in two occurrences in the ultrahigh-temperature Napier Complex of Antarctica. Monazite shows a variety of textures and compositions. In a garnet-sillimanite-orthopyroxene paragneiss at Mount Pardoe (Amundsen Bay), grains range 80–150 μm across and are anhedral; two grains are Th- and Si-dominant. In pods that crystallized from anatectic melts at 2500 Ma at Zircon Point, Casey Bay, monazite grains range 0.05 mm–1 cm in length and are highly variable in texture. The coarsest grains (>0.7 cm) are skeletal and euhedral, whereas the smallest grains are anhedral and associated with fine- to medium-grained quartz, K-feldspar, plagioclase, garnet, sillimanite and rutile in aggregates that form interstitial veinlets interpreted to be a second generation of anatexis during an event at 1100 Ma. The huttonite component (ThSiO4) reaches 30 mole% in the cores of the coarsest skeletal grains, whereas other grains, particularly smaller ones, show complex and irregular zoning in Th and U. The latter zoning is attributed to dissolution-reprecipitation, which also resulted in complete Pb loss during the 1100 Ma event. In the paragneiss at Mount Pardoe, K-feldspar and myrmekitic plagioclase (An16) are found in a 70–80 μm band between monazite and orthopyroxene and contain up to 12.7 wt.% and 2.7 wt.% PbO, respectively, corresponding to 18.5% and 3.4% PbAl2Si2O8 component, respectively. Cathodoluminescence of both feldspars increases with distance from a nearby monazite grain and is not correlated with Pb content. Incorporation of Pb in K-feldspar and plagioclase could be a result of diffusion, even though the monazite adjacent to feldspar apparently lost little Pb, i.e., Pb could have been transported by fluid from the Th-rich grains, which did lose Pb. In contrast to the paragneiss, cathodoluminescence correlates with Pb content of K-feldspar in aureoles surrounding skeletal monazite grains 0.7–1 cm across in anatectic pods at Zircon Point. Pb content of K-feldspar decreases monotonically to near detection limits within several millimetres of monazite grains; the greatest PbO concentration is attained in K-feldspar inliers and embayments in monazite, 8.8 wt.%, corresponding to 11.7% PbAl2Si2O8 component. Fine-grained quartz in the K-feldspar suggests that the mechanism for Pb incorporation involved breakdown of feldspar: Pb2+ + 2(K,Na)AlSi3O8 → PbAl2Si2O8 + 4SiO2 + 2(K,Na)+ . The smooth decrease of Pb in the aureoles is not characteristic of dissolution-reprecipitation, which is characterized by abrupt changes of composition, and it seems more likely that Pb was incorporated in K-feldspar by diffusion at 1100 Ma. We suggest a model whereby fluid introduced during the 1100 Ma event flowed along grain boundaries and penetrated mineral grains. Temperatures were sufficiently high, i.e., 700°C, assuming burial in the mid-crust, for the fluid to induce localized melting of quartzofeldspathic matrix of the anatectic pods. Loss of radiogenic Pb was complete. Some penetration of K-feldspar by aqueous fluid is suggested by the presence of scattered galena specks and by rays of turbidity emanating from monazite. Aqueous fluid or water-rich granitic melt may have mediated the diffusion of Pb in feldspar, but it did not cause dissolution-reprecipitation. Although Pb was mobilized by aqueous fluid or water-rich granitic melt, it was not entirely flushed from the immediate vicinity of the monazite, but nearly half was incorporated in adjacent feldspar. Fluid activity that could cause Pb loss in monazite does not always leave an obvious trace, i.e., hydrous minerals, such as sericite, are very sparse, and biotite is absent in the anatectic pods at Zircon Point. Nonetheless, electron microprobe dating of monazite from the pods could not detect the 2500 Ma age of original crystallization determined by isotopic dating.  相似文献   

2.
The eclogite facies assemblage K-feldspar–jadeite–quartz in metagranites and metapelites from the Sesia-Lanzo Zone (Western Alps, Italy) records the equilibration pressure by dilution of the reaction jadeite+quartz=albite. The metapelites show partial transformation from a pre-Alpine assemblage of garnet (Alm63Prp26Grs10)–K-feldspar–plagioclase–biotite±sillimanite to the Eo-Alpine high-pressure assemblage garnet (Alm50Prp14Grs35)–jadeite (Jd80–97Di0–4Hd0–8Acm0–7)–zoisite–phengite. Plagioclase is replaced by jadeite–zoisite–kyanite–K-feldspar–quartz, and biotite is replaced by garnet–phengite or omphacite–kyanite–phengite. Equilibrium was attained only in local domains in the metapelites and therefore the K-feldspar–jadeite–quartz (KJQ) barometer was applied only to the plagioclase pseudomorphs and K-feldspar domains. The albite content of K-feldspar ranges from 4 to 11 mol% in less equilibrated assemblages from Val Savenca and from 4 to 7 mol% in the partially equilibrated samples from Monte Mucrone and the equilibrated samples from Montestrutto and Tavagnasco. Thermodynamic calculations on the stability of the assemblage K-feldspar–jadeite–quartz using available mixing data for K-feldspar and pyroxene indicate pressures of 15–21 kbar (±1.6–1.9 kbar) at 550±50 °C. This barometer yields direct pressure estimates in high-pressure rocks where pressures are seldom otherwise fixed, although it is sensitive to analytical precision and the choice of thermodynamic mixing model for K-feldspar. Moreover, the KJQ barometer is independent of the ratio PH2O/PT. The inferred limiting a(H2O) for the assemblage jadeite–kyanite in the metapelites from Val Savenca is low and varies from 0.2 to 0.6.  相似文献   

3.
Dehydration melting of muscovite in metasedimentary sequences is the initially dominant mechanism of granitic melt generation in orogenic hinterlands. In dry (vapour-absent) crust, muscovite reacts with quartz to produce K-feldspar, sillimanite, and monzogranitic melt. When water vapour is present in excess, sillimanite and melt are the primary products of muscovite breakdown, and any K-feldspar produced is due to melt crystallization. Here we document the reaction mechanisms that control nucleation and growth of K-feldspar, sillimanite, and silicate melt in the metamorphic core of the Himalaya, and outline the microstructural criteria used to distinguish peritectic K-feldspar from K-feldspar grains formed during melt crystallization. We have characterized four stages of microstructural evolution in selected psammitic and pelitic samples from the Langtang and Everest regions: (a) K-feldspar nucleates epitaxially on plagioclase while intergrowths of fibrolitic sillimanite and the remaining hydrous melt components replace muscovite. (b) In quartzofeldspathic domains, K-feldspar replaces plagioclase by K+–Na+ cation exchange, while melt and intergrowths of sillimanite+quartz form in the aluminous domains. (c) At 7–8 vol.% melt generation, the system evolves from a closed to open system and all phases coarsen by up to two orders of magnitude, resulting in large K-feldspar porphyroblasts. (d) Preferential crystallization of residual melt on K-feldspar porphyroblasts and coarsened quartz forms an augen gneiss texture with a monzogranitic-tonalitic matrix that contains intergrowths of sillimanite+tourmaline+muscovite+apatite. Initial poikiloblasts of peritectic K-feldspar trap fine-grained inclusions of quartz and biotite by replacement growth of matrix plagioclase. During subsequent coarsening, peritectic K-feldspar grains overgrow and trap fabric-aligned biotite, resulting in a core to rim coarsening of inclusion size. These microstructural criteria enable a mass balance of peritectic K-feldspar and sillimanite to constrain the amount of free H2O present during muscovite dehydration. The resulting modal proportion of K-feldspar in the Himalayan metamorphic core requires vapour-absent conditions during muscovite dehydration melting and leucogranite formation, indicating that the generation of large volumes of granitic melts in orogenic belts is not necessarily contingent on an external source of fluids.  相似文献   

4.
Chemical diffusion of Pb has been measured in K-feldspar (Or93) and plagioclase of 4 compositions ranging from An23 to An93 under anhydrous, 0.101 MPa conditions. The source of diffusant for the experiments was a mixture of PbS powder and ground feldspar of the same composition as the sample. Rutherford Backscattering (RBS) was used to measure Pb diffusion profiles. Over the temperature range 700–1050°C, the following Arrhenius relations were obtained (diffusivities in m2s-1):Oligoclase (An23): Diffusion normal to (001): log D = ( – 6.84 ± 0.59) – [(261 ± 13 kJ mol –1)/2.303RT]Diffusion normal to (010): log D = ( – 3.40 ± 0.50) – [(335 ± 11 kJ mol –1)/2.303RT]Andesine (An43): Diffusion normal to (001): log D = ( – 6.73 ± 0.54) – [(266 ± 12 kJ mol –1)/2.303RT] Diffusion normal to (010) appears to be only slightly slower than diffusion normal to (001) in andesine.Labradorite (An67): Diffusion normal to (001): log D = ( – 7.16 ± 0.61) – [(267 ± 13 kJ mol –1)/2.303RT] Diffusion normal to (010) is slower by 0.7 log units on average.Anorthite Diffusion normal to (010): log D = ( – 5.43 ± 0.48) – [(327 ± 11 kJ mol –1)/2.303RT]K-feldspar (Or93): Diffusion normal to (001): log D = ( – 4.74 ± 0.52) – [(309 ± 16 kJ mol –1)/2.303RT] Diffusion normal to (010): log D = ( – 5.99 ± 0.51) – [(302 ± 11 kJ mol –1)/2.303RT]In calcic plagioclase, Pb uptake is correlated with a reduction of Ca, indicating the involvement of PbCa exchange in chemical diffusion. Decreases of Na and K concentrations in sodic plagioclase and K-feldspar, respectively, are correlated with Pb uptake and increase in Al concentration (measured by resonant nuclear reaction analysis), suggesting a coupled process for Pb exchange in these feldspars. These results have important implications for common Pb corrections and Pb isotope systematics. Pb diffusion in apatite is faster than in the investigated feldspar compositions, and Pb diffusion rates in titanite are comparable to both K-feldspar and labradorite. Given these diffusion data and typical effective diffusion radii for feldspars and accessory minerals, we may conclude that feldspars used in common Pb corrections are in general less inclined to experience diffusion-controlled Pb isotope exchange than minerals used in U-Pb dating that require a common Pb correction.  相似文献   

5.
Subsolidus and melting reactions involving calcic plagioclase in pelitic assemblages in the K-Na-Ca model system occur at higher temperatures than their K-Na counterparts. For the most calcic plagioclase compositions observed in high-grade pelitic rocks (An25-An40) the equilibria are rarely extended by more than 30 ° C above those in KA1O2-NaAlO2-Al2O3-SiO2-H2O, although all discontinuities in facies inferred for the K-Na system are continuously displaced when they involve Ca-bearing plagioclase. The maximum pressure-temperature overlap between muscovite dehydration and initial melting reactions occurs in the pressure range of 4–6 kbar between about 640 ° and 720 ° C. This provides optimum conditions for anatectic melt generation in felsic rocks of the appropriate compositions progressively metamorphosed in kyanite-sillimanite facies series. Progressive regional metamorphism at pressures of 2–4 kbar, corresponding to andalusite-sillimanite facies series, shows little overlap between muscovite dehydration and initial melting reactions. Consequently anatectic melt generation in andalusite-sillimanite facies series would require the participation of biotite in dehydration-melting reactions. Felsic intrusive rock in andalusite-sillimanite terranes could have risen upward from their anatectic sites in high grade kyanite-sillimanite facies series at depth. Many andalusite-sillimanite facies series terranes culminating in migmatites could represent upward movement of kyanite-sillimanite facies series rocks to shallower depths with uplift rates faster than cooling rates.  相似文献   

6.
Seven distinct phases of Variscan two-mica granite are recognized in the Guarda-Sabugal area. They intruded the Cambrian schist-metagraywacke complex, crystallized in the middle crust, and are syn- to late-D3 (309.2 ± 1.8 Ma), late-D3 (304–300 Ma) and late- to post-D3 (299 ± 3 Ma; ID-TIMS ages on zircon and monazite). Two of the granites, G2 and G5, are close in age and have similar Sr, Nd and O isotope characteristics but contrasting whole rock and mineral features and formed by sequential increasing degree of partial melting of a common metasedimentary protolith. During sequential melting Ti, total Fe, Mg, Ca, Zr, Zn, Sr, Ba and REE contents and (La/Yb)N increase and Si and Rb contents decrease, plagioclase becomes richer in anorthite and biotite and muscovite richer in Ti and Mg. Each of these granites evolved subsequently by fractional crystallization of quartz, K-feldspar, plagioclase, biotite and ilmenite, defining separate series G2–G3–G7 and G5–G6 containing late Sn-bearing differentiates. Two other granites G1 and G4 represent distinct pulses of magma with individual fractionation trends for major and trace elements and distinct (87Sr/86Sr)300, ?Nd300 and δ18O values.  相似文献   

7.
本文对丹凤地区秦岭岩群含柯石英超高压变质地体长英质片麻岩中的混合岩化长英质浅色体和含石榴子石暗色包体的花岗质脉体进行了详细的矿物学、地球化学和锆石U-Pb年代学以及Lu-Hf同位素研究。其中,长英质浅色体显示了近原位熔融的高硅、富钾的过铝质花岗岩地球化学特征;锆石的CL图像呈灰黑色,均匀无结构或云雾状内部结构,Th/U比值0. 008,并含有钾长石、斜长石、石英和磷灰石等包裹体,显示深熔锆石的特征;花岗质脉体暗色包体中的石榴子石显示核-边成分环带,其中核部成分与秦岭岩群长英质片麻岩中石榴子石成分一致,边部Sps含量升高,显示熔体改造或退变质扩散特征,寄主花岗质脉体显示重稀土强烈亏损的与石榴子石平衡的熔体特征,指示它们是秦岭岩群含石榴子石长英质片麻岩部分熔融的产物。锆石LA-ICP-MS定年得到长英质浅色体和花岗质脉体的结晶年龄分别为445±4Ma和420±1Ma,明显晚于本区的超高压变质时代,而与折返过程中麻粒岩相和角闪岩相退变质叠加的时代基本一致。结合区域地质和前人的研究成果,提出秦岭岩群在深俯冲板块的折返过程中,分别在445Ma和420Ma发生了两期部分熔融作用。  相似文献   

8.
In the Segura area, Variscan S-type granites, aplite veins and lepidolite-subtype granitic aplite-pegmatite veins intruded the Cambrian schist-metagraywacke complex. The granites are syn D3. Aplite veins also intruded the granites. Two-mica granite and muscovite granite have similar ages of 311.0 ± 0.5 Ma and 312.9 ± 2.0 Ma but are not genetically related, as indicated by their geochemical characteristics and (87Sr/86Sr)311 values. They correspond to distinct pulses of magma derived by partial melting of heterogeneous metapelitic rocks. Major and trace elements suggest fractionation trends for: (a) muscovite granite and aplite veins; (b) two-mica granite and lepidolite-subtype aplite-pegmatite veins, but with a gap in most of these trends. Least square analysis for major elements, and modeling of trace elements, indicate that the aplite veins were derived from the muscovite granite magma by fractional crystallization of quartz, plagioclase, K-feldspar and ilmenite. This is supported by the similar (87Sr/86Sr)311 and δ18O values and the behavior of P2O5 in K-feldspar and albite. The decrease in (87Sr/86Sr)311 and strong increase (1.6‰) in δ18O from two-mica granite to lepidolite-subtype aplite-pegmatite veins, and the behaviors of Ca, Mn and F of hydroxylapatite indicate that these veins are not related to the two-mica granite.  相似文献   

9.
The spatial and temporal changes in element and mineral concentrations in regolith profiles in a chronosequence developed on marine terraces along coastal California are interpreted in terms of chemical weathering rates and processes. In regoliths up to 15 m deep and 226 kyrs old, quartz-normalized mass transfer coefficients indicate non-stoichiometric preferential release of Sr > Ca > Na from plagioclase along with lesser amounts of K, Rb and Ba derived from K-feldspar. Smectite weathering results in the loss of Mg and concurrent incorporation of Al and Fe into secondary kaolinite and Fe-oxides in shallow argillic horizons. Elemental losses from weathering of the Santa Cruz terraces fall within the range of those for other marine terraces along the Pacific Coast of North America.Residual amounts of plagioclase and K-feldspar decrease with terrace depth and increasing age. The gradient of the weathering profile bs is defined by the ratio of the weathering rate, R to the velocity at which the profile penetrates into the protolith. A spreadsheet calculator further refines profile geometries, demonstrating that the non-linear regions at low residual feldspar concentrations at shallow depth are dominated by exponential changes in mineral surface-to-volume ratios and at high residual feldspar concentrations, at greater depth, by the approach to thermodynamic saturation. These parameters are of secondary importance to the fluid flux qh, which in thermodynamically saturated pore water, controls the weathering velocity and mineral losses from the profiles. Long-term fluid fluxes required to reproduce the feldspar weathering profiles are in agreement with contemporary values based on solute Cl balances (qh = 0.025-0.17 m yr−1).During saturation-controlled and solute-limited weathering, the greater loss of plagioclase relative to K-feldspar is dependent on the large difference in their respective solubilities instead of the small difference between their respective reaction kinetics. The steady-state weathering rate under such conditions is defined as
  相似文献   

10.
Advances in field observations and experimental petrology on anatectic products have motivated us to investigate the geochemical consequences of accessory mineral dissolution and nonmodal partial melting processes. Incorporation of apatite and monazite dissolution into a muscovite dehydration melting model allows us to examine the coupling of the Rb-Sr and Sm-Nd isotope systems in anatectic melts from a muscovite-bearing metasedimentary source. Modeling results show that (1) the Sm/Nd ratios and Nd isotopic compositions of the melts depend on the amount of apatite and monazite dissolved into the melt, and (2) the relative proportion of micas (muscovite and biotite) and feldspars (plagioclase and K-feldspar) that enter the melt is a key parameter determining the Rb/Sr and 87Sr/86Sr ratios of the melt. Furthermore, these two factors are not, in practice, independent. In general, nonmodal partial melting of a pelitic source results in melts following one of two paths in εNd-87Sr/86Sr ratio space. A higher temperature, fluid-absent path (Path 1) represents those partial melting reactions in which muscovite/biotite dehydration and apatite but not monazite dissolution play a significant role; the melt will have elevated Rb/Sr, 87Sr/86Sr, Sm/Nd, and εNd values. In contrast, a lower temperature, fluid-fluxed path (Path 2) represents those partial melting reactions in which muscovite/biotite dehydration plays an insignificant role and apatite but not monazite stays in the residue; the melt will have lower Rb/Sr, 87Sr/86Sr, Sm/Nd, and εNd values than its source. The master variables controlling both accessory phase dissolution (and hence the Sm-Nd system), and melting reaction (and hence the Rb-Sr systematics) are temperature and water content. The complexity in Sr-Nd isotope systematics in metasediment-derived melts, as suggested in this study, will help us to better understand the petrogenesis for those granitic plutons that have a significant crustal source component.  相似文献   

11.
Time studies were performed in the quinary system Qz-Or-Ab-An-H2O at kbars and T=665 ° and 660 ° C. Starting material was a mixture of quartz, alkali feldspar Or80 and plagioclase An31. The compositions of plagioclases of run products were determined and compared with the plagioclase of stable solidus conditions.The solidus of the granite system was fixed at P HäO=5 kbars using various plagioclase — and appropriate alkali feldspar — compositions besides quartz in the starting mixture (Fig. 1).The results of time studies (Table 3 and Fig. 3) reveal metastable melting in the granite system Qz-Or-Ab-An-H2O. Plagioclase melts almost stoichiometrically. The new plagioclase compositions formed during melting of cotectic compositions approach the theoretically expected stable plagioclase compositions only extremely slowly. An extrapolation of the data achieved in run times of 5–1,500 h indicates attainment of equilibrium after 1014 years. Metastable melting of granitic compositions is not only considered as an experimental problem but also as a rock forming process in nature.  相似文献   

12.
A detailed study based on textural observations combined with microanalysis [back scattered electron imaging (BSE) and electron microprobe analysis (EMPA)] and microstructural data transmission electron microscopy (TEM) has been made of K-feldspar micro-veins along quartz–plagioclase phase and plagioclase–plagioclase grain boundaries in granulite facies, orthopyroxene–garnet-bearing gneiss's (700–825 °C, 6–8 kbar) from the Val Strona di Omegna, Ivrea–Verbano Zone, northern Italy. The K-feldspar micro-veins are commonly associated with quartz and plagioclase and are not found in quartz absent regions of the thin section. This association appears to represent a localised reaction texture resulting from a common high grade dehydration reaction, namely: amphibole + quartz = orthopyroxene + clinopyroxene + plagioclase + K-feldspar + H2O, which occurred during the granulite facies metamorphism of these rocks. There are a number of lines of evidence for this. These include abundant Ti-rich biotite, which was apparently stable during granulite facies metamorphism, and total lack of amphibole, which apparently was not. Disorder between Al and Si in the K-feldspar indicates crystallisation at temperatures >500 °C. Myrmekite and albitic rim intergrowths in the K-feldspar along the K-feldspar–plagioclase interface could only have formed at temperatures >500–600 °C. Symplectic intergrowths of albite and Ca-rich plagioclase between these albitic rim intergrowths and plagioclase suggest a high temperature grain boundary reaction, which most likely occurred at the start of decompression in conjunction with a fluid phase. Relatively high dislocation densities (>2 × 109 to 3 × 109/cm2) in the K-feldspar suggest plastic deformation at temperatures >500 °C. We propose that this plastic deformation is linked with the extensional tectonic environment present during the mafic underplating event responsible for the granulite facies metamorphism in these rocks. Lastly, apparently active garnet grain rims associated with side inclusions of K-feldspar and quartz and an exterior K-feldspar micro-vein indicate equilibrium temperatures within 20–30 °C of the peak metamorphic temperatures estimated for the sample (770 °C). Contact between these K-feldspar micro-veins and Fe-Mg silicate minerals, such as garnet, orthopyroxene, clinopyroxene or biotite along the interface, is observed to be very clean with no signs of melt textures or alteration to sheet silicates. This lends support to the idea that these micro-veins did not originate from a melt and, if fluid induced, that the water activity of these fluids must have been relatively low. All of these lines of evidence point to a high grade origin for the K-feldspar micro-veins and support the hypothesis that they formed during the granulite facies metamorphism of the metabasite layers in an extensional tectonic environment as the consequence of localised dehydration reactions involving the breakdown of amphibole in the presence of quartz to orthopyroxene, clinopyroxene, plagioclase, K-feldspar and H2O. It is proposed that the dehydration of the metabasite layers to an orthopyroxene–garnet-bearing gneiss over a 4-km traverse in the upper Val Strona during granulite facies metamorphism was a metasomatic event initiated by the presence of a high-grade, low H2O activity fluid (most likely a NaCl–KCl supercritical brine), related to the magmatic underplating event responsible for the Mafic Formation; and that this dehydration event did not involve partial melting. Received: 15 February 2000 / Accepted: 26 June 2000  相似文献   

13.
During equilibration of K-feldspar, quartz and muscovite with dilute KCl-solutions, the change in pH of the solution was measured as a function of time. The resulting equilibrium constant, K T = aK + /aH +, is 104.21±0.06, 105.86±0.03 and 106.01±0.03 at 300, 60 and 30° C respectively (standard states at 1 bar) and are consistent with the best higher temperature data. At 30° C this constant is consistent with the aK + /aH + ratio of seawater. From K T and the activity of K + in seawater, a pH of 8.2 is calculated, essentially identical with the pH which results from dissolution of CaCO3 under atmospheric CO2-pressure. Consequently, detrital K-feldspar, quartz, muscovite, and calcite are stable in seawater. Apparently, the seawater pH is controlled by CaCO3 as well as K-feldspar, quartz and muscovite. Independently both equilibria show virtually the same pH, within the variability due to disordering, solid solution and surface energy effects.Assuming that the K-concentrations of pore solutions vary between about 4000 and 40 ppm, these solutions have alkalic pH-values in the temperature range between 30 and 300° C if K-feldspar, quartz and muscovite are present. In limestones the pH is fixed by the dissociation of CaCO3; the occasionally observed formation of K-feldspar in these rocks requires a minimum K-concentration of approximately 4 ppm.

Die Untersuchungen wurden am Department of Mineralogy and Geochemistry der Pennsylvania State University durchgeführt. Der erste Autor (H. E. Usdowski) bedankt sich für die freundliche Aufnahme und die ausgezeichneten Arbeitsmöglichkeiten. Besonderer Dank gilt Dr. George Helz für viele Diskussionen und manche Hilfe im Labor. Die Deutsche Forschungsgemeinschaft hat die Untersuchungen durch einen Forschungsauftrag unterstützt.  相似文献   

14.
The Sanandaj-Sirjan Zone (SSZ) trends northwestward in western Iran on the Precambrian to Paleozoic basement and exposes abundant I-type granitoids and calc-alkaline volcanic rocks that were most active during the Late Jurassic to Upper Cretaceous. The petrogenesis of the granitoids and associated volcanic rocks has been widely related to Neotethyan subduction beneath the Iranian plate. We report a geochronological and geochemical study of the Suffi abad granite (SLG) body that crops outs southeast of Sanandaj within the SSZ and is mainly composed of K-feldspar + quartz + plagioclase ± hornblende. The SLG, which shows a high-K calc-alkaline affinity, has LA-ICPMS zircon U–Pb ages ranging between 149 ± 2 and 144 ± 3 Ma and initial 87Sr/86Sr of ∼0.7024–0.7069 and 143Nd/144Nd of ∼0.5125–0.5127. These value correspond to an ?Nd (145 Ma) of +1.5 and +4.9, suggesting that the SLG originated from the juvenile crust or depleted mantle with a young TDM (650–900 Ma) over the subduction zone beneath the SSZ. Zircon saturation temperatures suggest that crystallization of the zircons, or emplacement of the host magmas, occurred at 560–750 °C, consistent with an intergrowth texture of K-feldspar and quartz that implies crystallization around the K-feldspar-quartz eutectic at lower temperatures. Overall, geochemical data suggest that crystallization of the hornblende and plagioclase played a role in magma differentiation. These data allow us to conclude that the high-K SLG did not originate directly from the juvenile mantle source as do most I-type, calc-alkaline granitoids, but more likely was produced from the partial melting of pre-existing I-type granitoids in the upper continental crust under low pressure conditions.  相似文献   

15.
Reaction textures, fluid inclusions, and metasomatic zoning coupled with thermodynamic calculations have allowed us to estimate the conditions under which a biotite–hornblende gneiss from the Kurunegala district, Sri Lanka [hornblende (NMg=38–42) + biotite (NMg=42–44) + plagioclase + quartz + K-feldspar + ilmenite + magnetite] was transformed into patches of charnockite along shear zones and foliation planes. Primary fluid inclusion data suggest that two immiscible fluids, an alkalic supercritical brine and almost pure CO2, coexisted during the charnockitisation event and subsequent post-peak metamorphic evolution of the charnockite. These metasomatic fluids migrated through the amphibolite gneiss along shear zones and into the wallrock under peak metamorphic conditions of 700–750 °C, 5–6 kbar, and afl H2O=0.52–0.59. This resulted in the formation of charnockite patches containing the assemblage orthopyroxene (NMg=45–48) + K-feldspar (Or70–80) + quartz + plagioclase (An28) in addition to K-feldspar microveins along quartz and plagioclase grain boundaries. Remnants of the CO2-rich fluid were trapped as separate fluid inclusions. The charnockite patches show the following metasomatic zonation patterns: – a transition zone with the assemblage biotite (NMg= 49–51) + hornblende (NMg = 47–50) + plagioclase + quartz + K-feldspar + ilmenite + magnetite; – a KPQ (K-feldspar–plagioclase–quartz) zone with the assemblage K-feldspar + plagioclase + orthopyroxene (NMg=45–48) + quartz + ilmenite + magnetite; – a charnockite core with the assemblage K-feldspar + plagioclase + orthopyroxene (NMg = 39–41) + biotite (NMg=48–52) + quartz + ilmenite + magnetite. Systematic changes in the bulk chemistry and mineralogy across the four zones suggest that along with metasomatic transformation, this process may have been complicated by partial melting in the charnockite core. This melting would have been coeval with metasomatic processes on the periphery of the charnockite patch. There is also good evidence in the charnockitic core that a second mineral assemblage, consisting of orthopyroxene (NMg= 36–42) + biotite (NMg=50–51) + K-feldspar (Or70–80) + quartz + plagioclase (An28–26), could have crystallised from a partial melt during cooling from 720 to 660 °C at decreasing afl H2O from 0.67 to 0.5. Post-magmatic evolution of charnockite at T < 700 °C resulted in fluids being released during the crystallisation of the charnockitic core. These gave rise to the formation of late stage rim myrmekites along K-feldspar grain boundaries as well as late stage biotite, cummingtonite, and carbonates. Received: 15 September 1999 / Accepted: 8 June 2000  相似文献   

16.
ABSTRACT

The Sarduiyeh granitoid (SG) is intruded in the southeastern part of the Dehaj-Sarduiyeh volcano-sedimentary belt in the southeastern end of the Urumieh-Dokhtar Magmatic Arc (UDMA) in Iran. The medium-to-coarse-grained granitoid unit, with granular texture consists mainly of diorite, tonalite, granodiorite and monzogranitic rocks. Mineralogically, these rocks consist mainly of plagioclase, K-feldspar, quartz, biotite and hornblende. The whole rock geochemical analyses indicates that the SG is calc-alkaline, I-type, metaluminous, enriched in large ion lithophile elements (LILE; such as K, Cs, Pb) and depleted in high field strength elements (HFSE; such as Ti, Nb, Ta, Zr). Chondrite normalized plot of SG rare earth elements (REE) show light rare earth element enrichments with (LaN/YbN = 2.44–8.68) and flat heavy rare earth element patterns with (GdN/YbN = 1.02–1.36). The rather high Y (av. 19.35 ppm), low Sr content (av. 293.76 ppm) and low Cr and Ni contents (av. 20.1 and 4.69 ppm, respectively) of the SG demonstrate its normal calc-alkaline and non-adakitic nature, the features of Jebal Barez-type granitoids. The geochemical characteristics and isotopic composition, low ISr (0.7046–0.7049) and positive ?tNd (+3.4 to +4.03) values, of the SG suggest that its parental magma formed as a result of partial melting from metabasic rocks of lower crust in a subduction-related arc setting. Fractionation of an assemblage dominated by plagioclase, K-feldspar, amphibole and magnetite may have been responsible for the evolution of the SG magma. U-Pb zircon geochronology gives an age of 27.95 ± 0.27 Ma for the SG, suggesting that the final collision between the Arabian plate and Central Iranian microcontinent may have happened in the Late Oligocene.  相似文献   

17.
The Shexian gneissic granodiorite in southern Anhui trends NE 55° from Shexian in the west to Guitoujian in the east with a length of 22 km and an outcrop area of 32 km. It was considered formerly to be Caledonian on the basis of a biotite K-Ar age of 474 Ma (1982). However, new evidence indicates that it may be Early Jinning in age as shown by: (1) it is found intruding into the Mid-Proterozoic Shangxi Group and is unconformably overlain by the Sinian Xiuning Formation, and (2) a zircon U-Th-Pb age of 928 Ma is obtained for the pluton. The pluton is composed of plagioclase (An=27.37%), K-feldspar(14%), biotite(16%) and quartz(32%). Accessory minerals are ilmenite (150g/T), xenotime (15g/T). garnet(25g/T), monazite(10g/T), zircon (20g/T) and apatite (104g/T). Petrochemical characteristics of the intrusion are:(l) Al-enrichment (A/NKC=1.30); (2) H2O enrichment (H2O= 1.74%); and (3) low oxidation index (f ’=0.10). It belongs to the continental crust transformation type as evidenced by: (1) MF and Mg/Y values of biotite are 0.41 and 0.31 respectively; (2) (87Sr/86Sr)=0.71119; (3) δ Eu=0.52; and (4) A/NKC=130. The Shexian pluton is therefore considered as a product of melting of phyllite at depth in the light of similarities in trace element and REE contents with the phyllite of the Banxi Group. Calculations of REE batch partial melting indicate that it may have resulted from 75% melting of the Banxi phyllite.  相似文献   

18.
Abstract Microprobe analyses of feldspars in granite mylonites containing flame perthite give compositions that invariably plot as three distinct clusters on a ternary feldspar diagram: orthoclase (Or92–97), albite and oligoclase-andesine. The albite occurs as grains in the matrix, as flame-shaped lamellae in orthoclase, and in patches within plagioclase grains. We present a metamorphic model for albite flame growth in the K-feldspar in these rocks that is related to reactions in plagioclase, rather than alkali feldspar exsolution. Flame growth is attributed to replacement and results from a combination of two retrograde reactions and one exchange reaction under greenschist facies conditions. Reaction 1 is a continuous or discontinuous (across the peristerite solvus) reaction in plagioclase, in which the An component forms epidote or zoisite. Most of the albite component liberated by Reaction 1 stays to form albite in the host plagioclase, but some Na migrates to form the flames within the K-feldspar. Reaction 2 is the exchange of K for Na in K-feldspar. Reaction 3 is the retrograde formation of muscovite (as ‘sericite’) and has all of the chemical components of a hydration reaction of K-feldspar. The Si and Al made available in the plagioclase from Reaction 1 are combined with the K liberated from the K-feldspar, to produce muscovite in Reaction 3. The muscovite forms in the plagioclase, rather than the K-feldspar, as a result of the greater mobility of K relative to Al. The composition of the albite flames is controlled by both the peristerite and the alkali feldspar miscibility gaps and depends on the position of these solvi at the pressure and temperature that existed during the reaction. Using an initial plagioclase composition of An20, the total reaction can be summarized as: 20 oligoclase + 1 K-feldspar + 2 H2O = 2 zoisite + muscovite + 2 quartz + 15 albiteplagioclase+ 1 albiteflame. This model does not require that any additional feldspar framework be accreted at replacement sites: Na and K are the only components that must migrate a significant distance (e.g. from one grain to the next), allowing Al to remain within the altering plagioclase grain. The resulting saussuritization is isovolumetric. The temperature and extent of replacement depends on when, and how much, water infiltrates the rock. The fugacity of the water, and therefore the pressure of the fluid, may have been significantly lower than lithostatic during flame growth.  相似文献   

19.
We investigate the inclusions hosted in peritectic garnet from metapelitic migmatites of the Kinzigite Formation (Ivrea Zone, NW Italy) to evaluate the starting composition of the anatectic melt and fluid regime during anatexis throughout the upper amphibolite facies, transition, and granulite facies zones. Inclusions have negative crystal shapes, sizes from 2 to 10 μm and are regularly distributed in the core of the garnet. Microstructural and micro‐Raman investigations indicate the presence of two types of inclusions: crystallized silicate melt inclusions (i.e., nanogranitoids, NI), and fluid inclusions (FI). Microstructural evidence suggests that FI and NI coexist in the same cluster and are primary (i.e., were trapped simultaneously during garnet growth). FI have similar compositions in the three zones and comprise variable proportions of CO2, CH4, and N2, commonly with siderite, pyrophyllite, and kaolinite, suggesting a COHN composition of the trapped fluid. The mineral assemblage in the NI contains K‐feldspar, plagioclase, quartz, biotite, muscovite, chlorite, graphite and, rarely, calcite. Polymorphs such as kumdykolite, cristobalite, tridymite, and less commonly kokchetavite, were also found. Rehomogenized NI from the different zones show that all the melts are leucogranitic but have slightly different compositions. In samples from the upper amphibolite facies, melts are less mafic (FeO + MgO = 2.0–3.4 wt%), contain 860–1700 ppm CO2 and reach the highest H2O contents (6.5–10 wt%). In the transition zone melts have intermediate H2O (4.8–8.5 wt%), CO2 (457–1534 ppm) and maficity (FeO + MgO = 2.3–3.9 wt%). In contrast, melts at granulite facies reach highest CaO, FeO + MgO (3.2–4.7 wt%), and CO2 (up to 2,400 ppm), with H2O contents comparable (5.4–8.3 wt%) to the other two zones. Our results represent the first clear evidence for carbonic fluid‐present melting in the Ivrea Zone. Anatexis of metapelites occurred through muscovite and biotite breakdown melting in the presence of a COH fluid, in a situation of fluid–melt immiscibility. The fluid is assumed to have been internally derived, produced initially by devolatilization of hydrous silicates in the graphitic protolith, then as a result of oxidation of carbon by consumption of Fe3+‐bearing biotite during melting. Variations in the compositions of the melts are interpreted to result from higher T of melting. The H2O contents of the melts throughout the three zones are higher than usually assumed for initial H2O contents of anatectic melts. The CO2 contents are highest at granulite facies, and show that carbon‐contents of crustal magmas are not negligible at high T. The activity of H2O of the fluid dissolved in granitic melts decreases with increasing metamorphic grade. Carbonic fluid‐present melting of the deep continental crust represents, together with hydrate‐breakdown melting reactions, an important process in the origin of crustal anatectic granitoids.  相似文献   

20.
In a prograde amphibolite-granulite transition zone in the Namaqualand Metamorphic Complex, metapelites show an interbanding of the amphibolite facies association biotite+sillimanite+quartz with the granulite facies association garnet+cordierite+K-feldspar. Relict graded bedding shows that compositional banding is of sedimentary origin. The garnet-cordierite-K-feldspar gneisses contain quartzofeldspathic segregations surrounding garnets, and have more Fe-rich bulk compositions than the biotite-sillimanite schists.The contrasting asemblages could have formed at the same pressure and temperature provided that a(H2O) was systematically lower in the garnet-cordierite-K-feldspar layers. The a(H2O) reduction resulted from the production of silicate melt by a vapour-absent continuous Fe-Mg reaction such as biotite+sillimanite+quartz=garnet+K-feldspar+liquid which affects Fe-rich compositions before vapour-absent melting occurs in more Mg-rich rocks. The segregations represent the solid and liquid products of the reaction.Such processes imply local control of a(H2O), and indicate that this granulite transition did not result from a regional influx of metasomatising fluids.  相似文献   

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