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1.
Major and trace element (Rb, Sr, Ba, Zr, Y, Nb, Ni, Co, V, Cr) data are presented for 11 spinifex-textured peridotites (STP) and a number of high-magnesian and low-magnesian tholeiitic basalts. The STP, representing high-magnesian liquids, come from the Yilgarn Block of Western Australia, Munro Township in the Abitibi Belt of Canada and one sample from the Barberton area of South Africa. All of the basaltic samples come from the Yilgarn Block.The STP and high-magnesian rocks are considered to belong to the komatiite suite (1, 2) despite their low CaO/Al2O3 ratios. It is argued that the high values (about 1.5) reported for this ratio from the Barberton area can be explained by a combination of factors, viz. garnet separation, Al loss or Ca addition during metamorphism. The processes can be evaluated using CaO/TiO2, Al2O3/TiO2 ratios, the REE group and trace elements (e.g. Y, Sc). It would appear that most STP from other Archaean belts do not have abnormal CaO/Al2O3 ratios.The STP display close to chondritic ratios for Ti/Zr, Zr/Nb, Zr/Y, and TiO2/Al2O3 and are considered to represent liquids produced by large amounts of partial melting of the Archaean mantle. The data suggest that virtually all phases other than olivine were removed by melting during the production of STP liquids. In the STP, Ti/V, Ti/P ratios are non-chondritic, suggesting original depletion and/or incorporation into the core.For lower levels of partial melting, including mid-ocean ridge basalts (MORB) non-chondritic ratios are exhibited by Zr/Y, TiO2/Al2O3, TiO2/CaO, suggesting controlling phases in the residue for Y, Ca, Al. It is apparent that for STP, Cr is not being controlled, indicating the absence of chromite in the residual. However, at about 15% MgO the data suggest that chromite becomes a residual phase.The transition metals, with the exception of Mn, have higher abundances in Archaean basaltic rocks than in MORB. This is interpreted as being mainly due to more extensive partial melting of the mantle in the Archaean, as a result of higher temperatures.It is suggested that the generation of STP liquids with about 32% MgO is due to upwelling mantle diapirs which probably originated at depths greater than 400 km and at temperatures in excess of 1900°C.Modern equivalents to Archaean greenstone sequences are lacking. The closest tectonic analogue would be the development of oceanic crust within a rifted continental block.  相似文献   

2.
This paper discusses the possibility of immobilization of TiO2 nanoparticles onto recycled wool‐based nonwoven material, which can be utilized for removal of dyes from wastewater. The photocatalytic activity of TiO2 nanoparticles deposited on the nonwoven material was evaluated in the aqueous solution of direct dye C.I. Direct Blue 78 under the UV illumination. Nonwoven material modified with TiO2 nanoparticles provides complete removal of dye from the solution already after 4–6 h of UV illumination. However, photodegradation of the dye adsorbed on the nonwoven material was obtained within 24 h of UV illumination. The rate of dye adsorption and photodegradation depends on the amount of deposited TiO2 nanoparticles. The increase of initial dye concentration induced decrease in photocatalytic efficiency of immobilized TiO2 nanoparticles. The highest photodegradation rate was achieved in acidic conditions. Elevated temperatures positively affected the removal of dye from solution. Photocatalytic activity of TiO2 nanoparticles deposited on nonwoven material was preserved after three photodegradation cycles.  相似文献   

3.
Pore water has been extracted from Boom Clay by mechanical squeezing. Clay cores were obtained from various boreholes, all drilled at the SCK·CEN domain (Mol, Belgium).In contrast to pore water collected from piezometers, high sulphate concentrations are measured in the squeezed pore water. The lowest sulphate concentrations (<60 mg/l) were measured in pore waters squeezed immediately after drilling. Higher sulphate concentrations were often measured in the pore water when the clay cores were preserved for some time (generally <500 mg/l SO42−, but sometimes up to 20,000 mg/l SO42−). Nevertheless, a relation between preservation time and sulphate content could not be retrieved. However, major ion concentrations were obviously correlated with the sulphate content in the squeezed waters. The observed evolution in chemical composition were explained by water–rock interactions considering the pyrite oxidation and the subsequent ion exchange and mineral dissolution reactions.  相似文献   

4.
Ag‐modified TiO2 nanotube arrays (Ag/TiO2 NAs) were prepared and employed as a photocatalyst for degradation of 17α‐ethinylestradiol (EE2) and inactivation of Escherichia coli. The as‐synthesized Ag/TiO2 NAs were characterized by field‐emission scanning electron microscope (FESEM), X‐ray diffraction (XRD), and X‐ray photoelectron spectroscopy (XPS). It was found that metallic Ag nanoparticles were firmly deposited on the TiO2 NAs with the pore diameter of 100 nm and the length of 550 nm. Photocatalytic degradation of EE2 and inactivation of E. coli were enhanced effectively in an analogical trend using Ag/TiO2 NAs. In particular, Ag/TiO2 NAs exhibited the antimicrobial activity even in the absence of light. The Ag acted as a disinfection agent as well as the dopant of the modified TiO2 NAs photocatalysis by forming a Schottky barrier on the surface of TiO2 NAs. Inorganic ions suppressed the rates of photocatalytic degradation of EE2, with HCO having a more pronounced effect than NO or SO. Humic acid (HA) was found to increase the rate of EE2 degradation.  相似文献   

5.
Highly toxic divalent cadmium causes serious environmental issues. To quickly monitor and/or efficiently remove this potentially toxic metal ion as well as to explore its interfacial chemistry with metal oxides, a sulfur and carbon co‐doped titania (S/C‐TiO2) composite is synthesized via a facile sol‐gel method with the assistance of sodium lignosulphonate (SLS). The prepared composite displays a well‐crystallized TiO2 nanostructure comprising the anatase phase. Both S and C, which are derived from the SLS template, are found to enter the TiO2 lattice. The S/C‐TiO2 composite exhibits a porous structure with a wide pore size distribution. The newly synthesized composite shows adsorption capability for the potentially toxic metal Cd(II). The adsorption process requires <5 min to reach equilibrium. The measured equilibrium adsorption capacity is 19.42 mg g?1, which is twice as high as that of bare TiO2. The removal efficiency is as high as 97%. Moreover, the materials are suitable for contaminated solutions over a wide range of pH values and various initial cadmium concentrations. A mechanism for the enhanced adsorption behavior is also proposed.  相似文献   

6.
Kaolin, cordierite, and calcite are investigated as supports for TiO2. The prepared TiO2/support samples are examined for the removal of organic dyes from wastewater. The samples are preliminarily investigated to identify the optimal loaded system using synthetic wastewater containing methylene blue (MB). Data indicate that the investigated support significantly affects the photocatalytic activity of the supported TiO2. Low photocatalytic activity toward MB degradation is observed upon using TiO2/calcite when compared to the unsupported TiO2. Interaction between calcite and titania species probably occurrs to produce the less photoactive CaTiO3 amorphous species. Anatase TiO2 is obtained upon using kaolin and cordierite as supports. The low photocatalytic performance of the TiO2/kaolin sample is also observed. A high concentration of MB on TiO2/kaolin surfaces blocks the photoactive sites. TiO2/cordierite shows the highest photocatalytic activity compared to the unsupported TiO2 as well as the other TiO2/support samples. Rigid cordierite particles suppress the agglomeration of TiO2 particles during the preparation, leading to a high exposed surface of TiO2 towards light illumination. TiO2/cordierite is investigated for the removal of organic dye from real wastewater collected from a textile dyeing factory. Color removal of up to 46% is achieved upon UV irradiation.  相似文献   

7.
Ti‐SBA‐15 materials with Ti incorporated into the framework of SBA‐15 and controllable Ti contents were successfully prepared via a post‐treatment route in supercritical CO2‐ethanol solution, followed by calcination. The resultant Ti‐SBA‐15 materials were characterized by means of different techniques including X‐ray diffraction, X‐ray photoelectron spectroscopy, transmission electron microscopy, IR analysis, and N2 sorption analysis. It was demonstrated that the resultant materials retained a structure similar to that of the parent SBA‐15, and Ti was incorporated into the framework of SBA‐15. At high Ti content, i.e, Si/Ti = 5:1, a TiO2 phase formed and was coated onto the inner surface of SBA‐15 in addition to the incorporation of the Ti in the framework. The BET surface areas of the Ti‐SBA‐15 samples decreased with increasing Ti content. The presence of small amounts of H2O in the reaction medium may have resulted in some TiO2 nanoparticles being uniformly distributed in the pores of the SBA‐15 accompanying the incorporation of Ti in the SBA‐15 framework.  相似文献   

8.
《Marine pollution bulletin》2012,64(5-12):303-308
In this study, zebrafish embryos were exposed to titanium dioxide nanoparticles (TiO2 NPs at 0.1, 0.5, 1, 5, 10 mg/L or control) from fertilization to free swimming stage. Hatchability, survival, and malformation rate were not affected by TiO2 NPs at these exposure levels. However, larval swimming parameters, including average and maximum velocity and activity level were significantly affected by TiO2 NPs. Co-exposure to either the glutathione precursor, N-acetylcysteine (NAC), or the glutathione synthesis inhibitor, buthionine sulfoximine (BSO), did not significantly alter the behavioral effects resulting from TiO2 NPs, suggesting that other factor(s) besides oxidative stress may contribute to the behavioral toxicity of TiO2 NPs. Our study also demonstrated that the behavioral endpoints were more sensitive than the others (e.g., hatchability and survival) to detect toxicity of TiO2 NPs on developing fish.  相似文献   

9.
The objective of this study was to investigate the effect of salt concentration on performance of a membrane bioreactor (MBR) for treating an olefin plant wastewater. For this purpose, a lab‐scale submerged MBR with a flat‐sheet ultrafiltration membrane was used for treatment of synthetic wastewater according to oxidation and neutralization unit of olefin plant. The synthetic wastewater was adjusted to have 500 mg/L chemical oxygen demand (COD). Trials on different concentrations of sodium sulfate (Na2SO4) (0–20 000 ppm) in the feed were conducted under aerobic conditions in the MBR. The results showed that increasing the salt concentrations causes an increase in the effluent COD, phenol, and oil concentrations. These results are due to reduction of the membrane filtration efficiency and also decline in the microbial activity that it is indicated by decreasing the sOUR in MBR. But in all the trials, the effluent COD and oil concentration was well within the local discharge limit of 100 and 10 mg/L, respectively. These results indicate that the MBR system is highly efficient for treating the olefin plant wastewater, and although high salt concentrations decreased organic contaminant removal rates in the MBR, the effluent still met the discharge limits for treating the olefin plant wastewater.  相似文献   

10.
In this study, the dechlorination of chlorinated hydrocarbon 3,3′,4,4′-tetrachlorobiphenyl (PCB77) by bimetallic Ni/Fe nanoparticles immobilized on L-lysine/PAA/PVDF membrane was investigated at ambient conditions through the batch mode operation. The membrane support polyvinylidene fluoride (PVDF) was modified by in situ polymerization of acrylic acid in aqueous phase, then L-lysine was covalently bonded to the polymerized acrylic acid chains with the aid of a water-soluble carbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC). The modification procedure involved cationic ion exchange with Fe2+, reduction to Fe0 with NaBH4 and finally deposition of Ni0. The scanning electron microscopic images showed that the Ni/Fe nanoparticles were successfully immobilized inside the membrane using the polyacrylic acid (PAA) as an inter-linkage between PVDF and L-lysine. A systematic characterization of the composite was performed using ATR-FTIR, HRSEM, EDX, HRTEM, XRD, and contact angle measurement studies and a relatively uniform distribution of Ni/Fe was found in L-lysine/PAA/PVDF membrane because of its hydrophilic nature. The obtained Ni/Fe nanoparticles consist of Fe0 core surrounded by the Ni0 shell. The diameter of Ni/Fe nanoparticles was predominantly within the range 20–30 nm. The immobilized Ni/Fe nanoparticles exhibited a good reactivity towards the dechlorination of the chlorinated hydrocarbon since the concentration of the PCB77 was decreased by catalytic dechlorination with Ni/Fe nanoparticles inside the L-lysine/PAA/PVDF membrane. Dechlorination efficiency of 98% was achieved within 9 h.  相似文献   

11.
Depth profiles of solute chemistry and sulfate isotopic compositions are presented for groundwater and pore water in a sequence of Quaternary glacial outwash sediments. Sand units show evidence for hydraulic connection to the surface and thus modern sources of solutes. Finer‐grained sediments show a general pattern of increasing solute concentrations with depth, with sulfate derived from ancient rainwater and pyrite oxidation in the soil/drift. In these sediments sulfate has undergone bacterial sulfate reduction (BSR) to produce biogenic sulfide. In clay sediments, with d10 ≤ 1·6 µm, high concentrations of sulfate and acetate now co‐exist, implying that BSR is inhibited. The correlation with smaller sediment grain size indicates that this is due to pore size exclusion of the sulfate reducing bacteria. Mechanical restriction of microbial function thus provides a fundamental limitation on microbial respiration in buried clay‐rich sediments, which acts as a control on the chemical evolution of their pore waters. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

12.
Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO2 abundances in spinels and high TiO2 and Na2O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.  相似文献   

13.
Water quality in South Africa and around the world continues to deteriorate due to contamination by organic, inorganic and microbial substances. While many efforts have been done to address water quality problems, current drinking water treatment technologies remain costly and do not effectively remove pollutants to acceptable levels. In this work nitrogen doped carbon nanotubes/polyethersulfone (N-CNT/PES) blend membranes were synthesized via a modified phase inversion method and assessed for suitability in drinking water treatment. The N-CNTs with outer diameters of 30–45 nm and 3% N content were prepared using a conventional chemical vapour deposition method and functionalized by refluxing in HNO3. The confirmation and degree of functionalization with –OH and –COOH groups was determined using Fourier-transform infrared (FTIR) spectroscopy and zeta potential analysis. FTIR studies confirmed the successful incorporation of functionalized N-CNTs (N-CNTs) in the membrane matrix. Atomic force microscopy (AFM) analysis revealed that the addition of N-CNTs leads to reduced surface roughness, suggesting a good dispersion of the N-CNTs in the matrix. Permeability studies revealed that the addition of N-CNTs to the polyethersulfone (PES) solution increased the water flux of the blend membrane by up to 70%. N-CNT loadings of 0.04 wt% in the blend membranes gave low surface contact angle of 55° and high fluxes. In addition, inclusion of N-CNTs enhanced the mechanical properties of the N-CNT/PES blend membranes. The use of N-CNTs in mixed matrix PES membranes is reported for the first time here. The result already suggests superior compatibility of the N-CNTs with PES compared to undoped CNTs, due to the high surface reactivity of the N-CNTs.  相似文献   

14.
Although the CaO/Al2O3 ratio of komatiites has been regarded as one of the distinguishing features of these rocks, a comparison of various komatiite and oceanic tholeiite analyses suggests that there is a continuum of ratios between the two. The extremely high MgO values of peridotitic komatiites suggest that they are the result of high degrees of partial melting of the mantle, leaving a harzburgitic residuum depleted in CaO and Al2O3, and hence preserving in the melt the original CaO/Al2O3 ratio of the parental material. Available chemical models of the mantle have CaO/Al2O3 ratios too low to explain the origin of komatiite by such a process. Shallow-level melting of a layered mantle in which clinopyroxene content decreases and garnet content increases with depth, may explain the chemistry of komatiites and related ultrabasic lavas.  相似文献   

15.
N-MORB-type metabasites are discovered in the Guoganjianian area, central Qiangtang, Tibet, which are mainly metagabbro with cumulate structure and metabasalt. The rocks are distributed nearly from west to east unconformably underlying the Wanghuling Group of upper Triassic. On the basis of geo- chemical analysis, we find that the content of SiO2 is 43.03%―53.42%, and TiO2 1%―2.67%, Al2O3 16.75%―21.52%, CaO 7.03%―11.13%, K2O 0.05%―0.38%; the REE pattern is slight depletion or flat, and the trace spider diagram is like that of N-MORB, so we consider that the metabasite was formed under the setting of mid-ocean ridge or adult back-arc basin, and it is the fragment of Paleo-Tethys ophiolite.  相似文献   

16.
This study illustrates the degradation of an azo dye, Reactive Yellow 81 (RY81), by the combined irradiation of UV‐C and ultrasound in the presence of homogeneous (Fe2+) and heterogeneous (TiO2, ZnO) catalysts. The efficiency of homogeneous and heterogeneous oxidation systems was evaluated in regard of the decolorization and mineralization of RY81. Decolorization followed pseudo‐first‐order kinetics with homogeneous and heterogeneous catalysts. Complete color removal was accomplished by homogeneous sonocatalytic and sonophotocatalytic oxidation processes with apparent rate constants of 0.96 × 10?3 and 46.77 × 10?3 s?1, respectively, in the presence of Fe2+. However, partial color removal was obtained by heterogeneous sonocatalytic, photocatalytic, and sonophotocatalytic oxidation processes with apparent rate constants of 2.32 × 10?3, 3.60 × 10?3, and 3.67 × 10?3 s?1, respectively, in the presence of ZnO. TiO2 had the worst catalytic effect of all of the oxidation processes. The addition of hydrogen peroxide increased the rate constants of the heterogeneous oxidation processes and decreased the rate constants of the homogeneous oxidation processes. RY81 mineralization was 62.8% for the US/UV/Fe2+ homogeneous oxidation process, which was the best oxidation process, whereas it was 43.5% for the US/UV/ZnO/H2O2 heterogeneous oxidation process within 2 h reaction time.  相似文献   

17.
The extensive, complex, continental flood basalt (CFB) province which occurs in Ethiopia and Yemen consists of Oligocene prerift volcanism related to the Africa–Arabia continental break-up. Basalts from the northwestern Ethiopian Plateau exhibit a particularly large range of compositions and, for the first time in the Afro-Arabian CFB province, low-Ti basalts have been encountered. Major and some trace element data have been used to identify distinct geochemical groups and evaluate the role of differentiation processes. Three magma types have been distinguished: two high-Ti groups (HT1 and HT2) and one low-Ti group (LT). The transitional to tholeiitic LT suite exhibits low TiO2 (1–2.6%), Fe2O3* (10.5–14.8%), CaO/Al2O3 (0.4–0.75), Nb/La (0.55–0.85) and high SiO2 (47–51%). In contrast, the HT2 suite exhibits high TiO2 (2.6–5%), Fe2O3* (13.1–14.7%), CaO/Al2O3 (0.9–1.43), Nb/La (1.1–1.4) and low SiO2 (44–48.3%). The HT1 series is intermediate between the LT and HT2 groups. These three groups of lavas originated from different parental magmas. They display distinct differentiation trends, either controlled by the removal of a shallow level gabbroic (Pl+Ol+Cpx) assemblage (LT and HT1 suites) or by deeper Ol+Cpx fractionation (HT2 suite). Most of this thick continental flood lava pile was emplaced over a short time interval (about 1–2 Ma). The three contrasted magma types do not reflect a temporal evolution of their sources but rather a strong spatial control. Indeed, the northwestern Plateau may be subdivided into two different subprovinces as all the low-Ti basalts are located in the northern part of the plateau, and the high-Ti basalts are exposed in the eastern and southern parts. The LT and HT1 basalts display compositional ranges similar to those of the low- and high-Ti groups from other main CFB provinces (e.g. Parana, Deccan, Karoo, Siberia, …). However, the HT2 group exhibits extreme OIB-like compositions. This unusual geochemical signature suggests the involvement of deep mantle in the genesis of the HT2 magmas. The LT compositions rather reflect the participation of the continental lithosphere, through mantle derived melts and/or crustal contamination.  相似文献   

18.
The concept that the plutonism of the lunar highlands and the mare-type volcanism are two separate problems in both time (> 4.4 AE versus < 3.95 AE) and space is seriously questioned by the discovery of a 4.23-AE low-Ti mare basalt from Fra Mauro Formation.Apollo 14 breccia 14305 contains a clast (,122) which is an olivine gabbronorite that is texturally and mineralogically similar to several Apollo 12 basalts (e.g., 12005, 12035, 12040). It consists of cumulus olivine (40 modal %; Fo 62–70) and Ti-chromite (2.5 modal %); post-cumulus phases include low-Ca pyroxene (29 modal %; Wo 7–13 En 68–75), augite (10 modal %; Wo 31–40 En 47–50), plagioclase (15 modal %, An 82–93), and ilmenite (4 modal %, 5–7 MgO). The TiO2 content of this rock = 4.3%; CaO/Al2O3 ? 1.0, CaO = 5.1%; MgO/FeO ? 1.0, MgO = 21.9%. The REE pattern, normalized to chondritic abundances, is approximately 30 × Ch and “hump-shaped” with a pronounced Eu depletion and a non-KREEPy signature. A four-point Rb-Sr isochron reveals an age of 4.23 ± 0.05 AE. The sample has a low initial 87Sr/86Sr= 0.69911 ± 3.The data presented here show that non-KREEPy, mare-type volcanism commenced at least as early as 4.2 AE in the Fra Mauro region and probably across much of the lunar surface. Massive bombardment during the “terminal cataclysm” and the subsequent veneer of younger mare basalts has obliturated most of the evidence for these ancient volcanic events. These old, mare-type volcanics may be related to basin-forming events such as made Procellarum (i.e., impact-triggered igneous activity).  相似文献   

19.
Two main routes of methods for the preparation of photocatalytic active titanium dioxide films on glass substrates were investigated: (1) the use of titanium dioxide powder and (2) the in situ generation of the catalyst via hydrolysis of titanium tetraisopropoxide (TTIP) or TiCl4. The activities of the catalyst films were evaluated by measuring the degradation of dichloroacetic acid (DCA), clofibric acid, and terbuthylazine used as model organic compounds. The concentration decrease of DCA and the concentration increase of chloride ions as the decomposition product allowed to distinguish between photocatalytic degradation of DCA and adsorption onto the TiO2 films. Furthermore, TiO2 films of the commercially available materials P25 (Degussa) and Hombikat UV100 (Sachtleben Chemie) were used to investigate whether there was a difference in the degradation pathways of terbuthylazine as a model compound. For the experiments mini flow‐through reactors were constructed. The investigated immobilization techniques were easy to handle without need of any expensive equipment. All TiO2 coatings showed good photocatalytic activities and mechanical stabilities with efficient long‐term stabilities. The best immobilization reproducibility was achieved by the spray coating technique and by the in situ method with the dipping sol‐gel process starting by TTIP. During the continuous use of the TiO2 films no TiO2 particles were found in the irradiated solutions.  相似文献   

20.
Ocean-floor basalts and glasses were recovered from three stations along the western Nazca plate, from a sublinear topographic feature believed to represent the proto-East Pacific Rise (EPR), and include abyssal tholeiites, FeTi-basalts and glasses, as well as transitional and little fractionated compositions. When compared with their coexisting fresh glasses, the FeTi-basalts have higher total alkalies, TiO2 and MgO, and lower FeO*, suggesting that they have also been affected by non-oxidative post-magmatic alteration processes. The FeTi-glasses form a remarkably uniform compositional group through space and time. A little fractionated composition having anMg-number= 73, similar to those reported from the Mathematician Ridge, has higher Na2O and TiO2, and slightly lower CaO than similar compositions from the slowly accreting Mid-Atlantic Ridge. The basalts and glasses reported here exhibit the compositional diversity expected for propagating rifts and probably represent more than one volcanic episode.Both geochemical and geophysical interpretations support the inference that the EPR grew from Miocene times by the progressive growth and propagation of mantle perturbations, leaving a remnant sublinear zone of rough topography characteristic of slower accretion as the trace of the proto-EPR. Continuing translations and rotations of axial segments are occurring along the EPR, probably in response to self-reorganizations of mantle flow patterns arising from rapid melting and depletion of the source regions. The data allow the inference that the youthful rift systems of the eastern Pacific are far from thermodynamic equilibrium as might be expected if such systems were to drive fundamental life processes.  相似文献   

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