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1.
Todorokite is a common manganese oxide in soils, sediments, and marine manganese nodules. The MnO6 octahedrons share edges within chains and share cor-ners between chains to form a 3×3 tunnel framework of todorokite. Octahedral molecular sieves with struc-ture of todorokite exhibit superior characteristics in ion exchange, specific surface area, thermal stability and molecule-sized tunnels[1]. Todorokite plays an important role in cleaning up natural water and con-trolling concentration of h…  相似文献   

2.
A microprobe study of metalliferous sediment components   总被引：1，自引：0，他引：1  
Smectite aggregates, Fe-Mn micronodules, and fish debris from the coarse fraction of a metalliferous sediment sample from the Bauer Basin have been analyzed by microprobe. Both X-ray diffraction and bulk chemical analyses reveal that the smectite, an iron-rich and aluminum-poor nontronite, is the dominant phase. A linear programming solution to a series of mass balance equations indicates that the bulk sample is 70% smectite, 4% todorokite, 13% microlaminated material, and 1% fish debris. Two episodes of micronodule development are indicated by the presence of overgrowths of microlaminated iron-rich material over a homogeneous dense todorokite core. The two micronodule compositions can be explained by reaction of hydrothermally produced amorphous Fe-Mn oxyhydroxides with biogenous opal to form the calculated phase composition. The rare earth elements in the bulk sample can be explained by a similar diagenetic process which distributes rare earth elements of a seawater origin between cerium-enriched micronodules and cerium-depleted fish debris.  相似文献   

3.
Interiors of manganese nodules from siliceous ooze beneath the Pacific equatorial high-productivity region, when examined by scanning electron microscopy (SEM) and electron microprobe, display post-depositional recrystallization textures and metalliferous oxide bands (diameter 1–10 μm, 30–40 wt.% Mn, 4–5% Ni, 3–4% Cu). SEM has revealed biogenic siliceous matter in all stages of degradation and dissolution within nodule interiors, creating cavities and voids. Often these miniature vugs contain authigenic phillipsite crystallites which are coated with delicate clusters of crystalline Mn-Fe oxides (todorokite) containing significant amounts of Ni and Cu. We postulate the following diagenetic processes and mechanism of uptake of transition metals inside manganese nodules: (1) palagonite + biogenic silica + pelagic clay → phillipsite + montmorillonite; (2) biogenic matter + amorphous FeOOH or δ-MnO2 → Feaq2+ and/or MnIIMnIV oxide (todorokite); (3) aerated seawater or δ-MnO2 + Feaq2+ → FeOOH and/or todorokite (deposited on phillipsite); (4) (NiII and CuII) organic chelates (adsorbed on clays, etc.) + amorphous FeOOH or δ-MnO2 → Ni-Cu-todorokite + phillipsite, etc.This mechanism explains the well-known positive Mn-Ni-Cu and negative Fe-Ni, Fe-Cu correlations in nodules. By analogy with terrestrial todorokites, which require about 8 wt.% Mn to be in the divalent state to stabilize the crystal structure, as much as 8 wt.% (Ni + Cu) could be accommodated in todorokite-bearing deep-sea manganese nodules. However, although such nodules beneficiate Ni and Cu with respect to marine sediments and seawater, they remain undersaturated in these divalent cations.  相似文献   

4.
Clay aquitards are semipermeable membranes that allow groundwater flow while retarding solute migration has been researched extensively but also subjected to much debate. At present, there is no evidence of whether the physical and chemical properties of clay soil and the isotopic composition of pore water affect the semipermeable membrane effect. In this study, we collected clay samples from drilling cores (30–90 m) in the Hengshui area located in the North China Plain (NCP), then extracted pore water using a high-pressure squeezing device. Vertical hydrochemical and isotopic profile variation trends for the pore water were revealed using hydrochemical (Cl−, Na+, Ca2+, K+, Mg2+, and SO42−) and stable isotopic measurements of H, O and Cl. The results showed that the hydrochemical clay interlayer pore water of the saline aquifer is Cl/SO4-Na/Mg type and the average total dissolved solids (TDS) are 10.17 g/L. However, the hydrochemical clay aquitard pore water is of the Cl/SO4-Na/Ca type with an average TDS of 1.90 g/L. The hydrochemical clay interlayer pore water of aquifer II is of Cl-Na/Ca type with an average TDS of 1.10 g/L. Our results showed that the water quality of the aquifer II is not affected by the upper part of the saline aquifer, thus the clay aquitard acts as a significant barrier to salt movement. A polarization layer concentrated in ions was formed between the upper part of the saline aquifer and the clay aquitard. The concentration polarization layer increases the salt-inhibition effect. H, O and Cl isotopic composition results showed significant fractionation. The pore water of aquifer II lacked heavy isotopes (2H, 18O, 37Cl), but had significant heavy isotope enrichment in the concentrated polarized layer (the δ2H value was −76‰, the δ18O value was −8.4‰, and the δ37Cl value was 1.59‰). Hyperfiltration thus played a significant role in isotope fractionation.  相似文献   

5.
The oxidation state of iron can significantly influence the physical and chemical properties of lower mantle minerals. To improve methods for estimation of Fe3+/∑Fe, synthetic assemblages of (Mg,Fe)(Si,Al)O3 perovskite and (Mg,Fe)O ferropericlase were synthesised from oxide starting mixtures in Re or Fe capsules at 26 GPa and 1650-1850 °C using a multianvil press. (Mg,Fe)(Si,Al)O3 majorite was also present in some of the run products. Both electron energy loss spectra (EELS) and Mössbauer spectra were measured for each run product, and a robust fitting method was developed for Mössbauer spectra using EELS results as a standard that enabled Fe3+/∑Fe of (Mg,Fe)(Si,Al)O3 perovskite to be determined from Mössbauer spectra of multiphase assemblages. There is a close to linear variation between Fe3+/∑Fe and Al concentration in (Mg,Fe)(Si,Al)O3 perovskite, independent of oxygen fugacity. The concentration of Fe3+ in (Mg,Fe)O increases with increasing iron concentration along curves of constant oxygen fugacity, where higher oxygen fugacity stabilises greater Fe3+ concentrations. Fe2+/Mg partition coefficients calculated from chemical composition data corrected for measured Fe3+/∑Fe showed values nearly identical within experimental error for all samples, and independent of Al concentration and oxygen fugacity. Simple empirical relations were derived to calculate Fe3+/∑Fe in (Mg,Fe)(Si,Al)O3 perovskite and (Mg,Fe)O ferropericlase samples for which no Mössbauer or EELS data were available, and tested by applying them to calculation of Fe2+/Mg partition coefficients from literature data for (Mg,Fe)(Si,Al)O3 perovskite-(Mg,Fe)O assemblages where only total iron concentrations had been measured. Results showed Fe2+/Mg partition coefficients that were equal to existing values within experimental error, hence confirming the validity of the empirical relations.  相似文献   

6.
The degree of impact-induced devolatilization of nonporous serpentine, porous serpentine, and deuterium-enriched serpentine was investigated using two independent experimental methods, the gas recovery method and the solid recovery method, yielding consistent results. The gas recovery method enables determination of the chemical and hydrogen isotopic composition of the recovered gases. Experiments on deuterium-enriched serpentine unambiguously identify the samples as the source of the recovered gases, as opposed to other possible contaminants. For shock pressures near incipient devolatilization (Pinitial = 5.0 GPa), the hydrogen isotopic composition of the evolved gas is similar to that of the starting material. For higher shock pressures the bulk evolved gas is significantly lower in deuterium than the starting material. There is also significant reduction of H2O to H2 in gases recovered at higher shock pressures, probably caused by reaction of evolved H2O with the metal gas recovery fixture. The hydrogen isotopic fractionation between the evolved gas and the residual solid indicates nonequilibrium, kinetic control of gas-solid isotopic ratios. In contrast, gaseous H2O-H2 isotopic fractionation suggests high temperature (800-1300 K) isotopic equilibrium between the gaseous species, indicating initiation of devolatilization at sites of greater than average energy deposition (i.e., shear bands). Impact-induced hydrogen isotopic fractionation of hydrous silicates during accretion can affect the distribution of hydrogen isotopes of planetary bodies during accretion, leaving the interiors enriched in deuterium. The significance of this process for planetary development depends on the models used for extrapolation of the observed isotopic fractionation to devolatilizations greater than those investigated experimentally and assumptions about timing and rates of protoatmosphere loss, frequency of multiple impacts, and rates of gas-solid or gas-melt isotopic re-equilibration. A simple model indicates that substantial planetary interior enrichments of D/H relative to that of the incident material can result from impact-induced hydrogen fractionation during accretion.  相似文献   

7.
A portable Wavelength Scanned‐Cavity Ring‐Down Spectrometer (Picarro L2120) fitted with a diffusion sampler (DS‐CRDS) was used for the first time to continuously measure δ18O and δ2H of stream water. The experiment took place during a storm event in a wet tropical agricultural catchment in north‐eastern Australia. At a temporal resolution of one minute, the DS‐CRDS measured 2160 δ18O and δ2H values continuously over a period of 36 h with a precision of ±0.08 and 0.5‰ for δ18O and δ2H, respectively. Four main advantages in using high temporal resolution stream δ18O and δ2H data during a storm event are highlighted from this study. First, they enabled us to separate components of the hydrograph, which was not possible using high temporal resolution electrical conductivity data that represented changes in solute transfers during the storm event rather than physical hydrological processes. The results from the hydrograph separation confirm fast groundwater contribution to the stream, with the first 5 h of increases in stream discharge comprising over 70% pre‐event water. Second, the high temporal resolution stream δ18O and δ2H data allowed us to detect a short‐lived reversal in stream isotopic values (δ18O increase by 0.4‰ over 9 min), which was observed immediately after the heavy rainfall period. Third, δ18O values were used to calculate a time lag of 20 min between the physical and chemical stream responses during the storm event. Finally, the hydrograph separation highlights the role of event waters in the runoff transfers of herbicides and nutrients from this heavily cultivated catchment to the Great Barrier Reef. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

8.
Numerical modeling of mantle convection by Liu (1994, Science, 264: 1904–1907) favors a two-layer convection, if the results are reinterpreted for the correct phase relations in (Mg,Fe)2SiO4. The resulting chemical isolation of the upper and lower mantle suggests a highly differentiated and layered upper mantle to account for the discrepancy between the observed compositions of mantle xenoliths and the cosmic abundances of elements. It is shown that a layered upper mantle with a hidden reservoir can have a structure consistent with the observed seismic velocity profiles and an average bulk composition corresponding to the cosmic abundances. The evolution of the upper mantle and the origin of komatiites are discussed in the context of the proposed model.  相似文献   

9.
The increment method is adopted to calculate oxygen isotope fractionation factors for mantle minerals, particularly for the polymorphic phases of MgSiO3 and Mg2SiO4. The results predict the following sequence of18O-enrichment:pyroxene (Mg, Fe, Ca)2Si2O6>olivine (Mg, Fe)2SiO4 > spinel (Mg, Fe)2SiO4> ilmenite (Mg, Fe, Ca) SiO3>perovskite (Mg, Fe, Ca) SiO3. The calculated fractionations for the calcite-perovskite (CaTiO3) System are in excellent agreement with the experimental calibrations. If there would be complete isotopic equilibration in the mantle, the spinel-structured silicates in the transition zone are predicted to be enriched in18O relative to the perovskite-structured silicates in the lower mantle but depleted in18O relative to olivines and pyroxenes in the upper mantle. The oxygen isotope layering of the mantle might result from differences in the chemical composition and crystal structure of mineral phases at different mantle depths. Assuming isotopic equilibrium on a whole earth scale, the chemical structure of the Earth’s interior can be described by the following sequence of18O-enrichment:upper crust>lower crust>upper mantle>transition zone>lower mantle>core. Project supported by the National Natural Science Foundation of China and the Chinese Academy of Sciences.  相似文献   

10.
Different opinions exist regarding the specific effect of Mg on soil physical and chemical properties. We hypothesized that Mg2+, compared with Ca2+, reduces saturated hydraulic conductivity (Ks) via promoting clay swelling, disaggregation, and clay dispersion. Two soils (mixed, mesic Typic Hapludalfs) in packed soil columns were leached with either Ca- or Mg-containing solutions at the successive concentrations of 250, 10, 2, 0.5, and 0 mM. Critical flocculation concentration (CFC) in either Ca or Mg systems was determined with flocculation series tests. Aggregate stability and mean weight diameter (MWD) were assessed by wet-sieving. The CFCs were higher in Mg than in Ca for both soils, indicating that Mg is more dispersive than Ca. The MWDs measured using 1–2 mm aggregates of both soils were significantly larger for Ca-soils than for Mg-soils (P=0.05). The Ksr (normalized with initial Ks) started to decline at higher concentrations for Mg than for Ca, and the reduction was much greater in Mg than in Ca above 0.5 mM. The Ksr and percent transmittance (inversely related to turbidity) of leachate at a given eluted pore volume following ‘steady state’ were higher in Ca than in Mg for both soils (P=0.1), indicating lower permeability and more clay dispersion with the Mg treatment. Swelling and disaggregation, which reduced large pores, appeared to be the dominant process causing the rapid initial decline of Ksr. Clay dispersion and subsequent pore plugging became progressively important when electrolyte concentration was reduced to below CFCs.  相似文献   

11.
The microstructure charateristics of illite from the Chuanlinggou Formation of Changcheng System (Chch) in Jixian County, Tianjin City has been studied by means of high-resolution transmission electron microscopy (HRTEM), selected-area electron diffraction (SAED), X-ray energy dispersive spectrum (EDS) and X-ray powder diffraction (XRD). The Kübler index of "illite crystallinity" is 0.505°△2θ, which indicates that the host rock is in a middle diagenetic stage. The chemical analyses of EDS for illite studied indicate a heavily absent in interlayer cation and an average chemical formula of K0.57(Al1.80Mg0.42Fe2 0.12)Σ=2.34 (Si2.92Al1.08)Σ=4O10(OH)2. It is found, from one-dimensional lattice images, that the layers of illite not only stack in a flat way but also in a curving way. A "matting fabric" illite structure results from stacking faults. Combined with SAED analysis the illite studied can be affirmed as 1M illite. The two-dimensional lattice images are obtained from [100] and [110] incidences, whose lattice images have the same d-values but different intersecting angles. The two-dimensional lattice image with [100] incidence is orthogonal to each other, whilst that with [110] incidence is oblique. This paper provides some important structure information of authigenic clay minerals for the well-known mesoproterozoic section of Jixian County.  相似文献   

12.
Existing experimental evidence suggests that in pure Mg-forsterite with a fixed Mg/Si ratio, vacancies and interstitials on the Mg sublattice are the dominant intrinsic point defects, while O vacancies and conduction-band electrons are the primary oxygen-deficient defects. Orthopyroxene appears to dissolve readily in pure Mg-forsterite at high temperatures, the change in Mg/Si ratio being accommodated by Mg vacancies and Si interstitials; as a consequence, upper-mantle forsterite may be substantially non-stoichiometric. It is postulated that the amount of Fe that can be oxidized in the forsterite phase is directly related to the excess Si present, either incorporated in the structure, or available from another phase richer in SiO2 such as pyroxene.  相似文献   

13.
The Zargoli granite, which extends in a northeast–southwest direction, intrudes into the Eocene–Oligocene regional metamorphic flysch‐type sediments in the northwest of Zahedan. This pluton, based on modal and geochemical classification, is composed of biotite granite and biotite granodiorite, was contaminated by country rocks during its emplacement, and is slightly changed to more aluminous. The SiO2 content of these rocks range from 62.4 to 66 wt% with an alumina saturation index of Shand [molar Al2O3/(CaO + Na2O + K2O)] ～ 1.1. Most of its chemical variations could be explained by fractionation or heterogeneous distribution of biotite. The features of the rocks resemble those which are typical to post‐collisional granitoids. Chondrite‐normalized rare‐earth element patterns of these rocks are fractionated at (La/Lu)N = 2.25–11.82 with a pronounced negative Eu anomaly (Eu/Eu* = 3.25–5.26). Zircon saturation thermometry provides a good estimation of magma temperatures (767.4–789.3°C) for zircon crystallization. These characteristics together with the moderate Mg# [100Mg/(Mg + Fe)] values (44–55), Fe + Mg + Ti (millications) = 130–175, and Al–(Na + K + 2Ca) (millications) = 5–50 may suggest that these rocks have been derived from the dehydration partial melting of quartz–feldspathic meta‐igneous lower crust.  相似文献   

14.
Two synthetic pyroxenes (FeSiO3, MgSiO3) and five natural pyroxenes with compositions of about Fs80En20, Fs60En40, Fs50En50, Fs40En60, and Fs20En80 have been subjected to pressures up to250 ± 50kbars at a temperature of about1500 ± 200°C in a diamond anvil cell heated by an infrared laser beam. After quenching and unloading X-ray data analysis indicates that (1) those with Mg less than 50% undergo the following reactions: 2(Mg,Fe)SiO3 (pyroxene) → (Mg,Fe)2SiO4 (spinel) + SiO2 (stishovite) → 2(Mg,Fe)O (magnesiowu¨stite) + SiO2 (stishovite) with increase of pressure, and (2) those with Mg higher than 60%, undergo the following reactions: 2(Mg,Fe)SiO3 (pyroxene) → (Mg,Fe)2SiO4 (spinel) + SiO2 (stishovite) → 2(Mg,Fe)SiO3 (hexagonal phase) → 2(Mg,Fe)O (magnesiowu¨stite) + SiO2 (stishovite) with increase of pressure.  相似文献   

15.
This paper presents a field study conducted in northwest Turkey and characterizes the NH3 concentration and emission measured in summer season from three chicken farms. The influence of environmental conditions on NH3 concentration and emission was also investigated in this study. Ammonia concentration, temperature, relative humidity and airflow rate were continuously recorded for four sequential days. The environmental conditions were measured using a multifunction temperature and humidity‐meter with a hot wire probe. Portable multiple gas detectors with electro‐chemical sensors were used to measure NH3 concentration. The NH3 emission rates for houses were calculated by multiplying simultaneously measured NH3 concentrations and air flow rates. The average daily mean (ADM) house concentrations of house 1 (H1), house 2 (H2), and house 3 (H3) were measured as 4.43, 3.71, and 6.20 ppm, respectively. NH3 concentration was inversely proportional to temperature (r = ?0.279), relative humidity (r = ?0.063) and airflow rate (r = ?0.554) for all monitored houses. The ADM house NH3 emission was 135 g/(h house) for H1, 255 g/(h house) for H2, and 117 g/(h house) for H3. The combined average emission rate in this study (0.26 g/(d bird)) was lower than the emission rate measured in chicken farms in the USA. However, our results were comparable to rates calculated in European studies because house design, ventilation system and bird diet applied in Turkish chicken farms are very similar to those employed in European countries. The NH3 emissions were significantly correlated to NH3 concentrations (r = 0.45, p ≤ 0.001) and airflow rates (r = 0.97, p ≤ 0.001). A clear diurnal pattern was obtained for NH3 concentrations rather than NH3 emissions at the end of the study.  相似文献   

16.
The rheology of the lower mantle of the Earth is examined from the viewpoint of solid state physics. Recent developments in high-pressure research suggest that the lower mantle contains a considerable amount of (Mg, Fe)O with Fe/Mg + Fe = 0.2–0.3. The pressure and temperature dependences of diffusion in (Mg, Fe)O are estimated by the theory of diffusion in ionic solids. Of the materials composing the lower mantle, (Mg, Fe)O may be the “softest”, and therefore the rheology of the lower mantle may be that of (Mg, Fe)O, unless the framework effect is important.Temperatures in the lower mantle are inferred from the depths of phase transitions and the melting temperatures of the core materials. A thermal boundary layer at the base of the mantle is suggested. The physical mechanisms of creep are examined based on a grain size-stress relation and non-Newtonian flow is shown to be the dominant flow mechanism in the Earth's mantle.The effective viscosity for the temperature models, with and without the thermal boundary layer, is calculated for constant stress and constant strain rate (with depth). For constant strain rate, which may be appropriate for discussing the mechanics of descending slabs, the increase in effective viscosity with depth is smaller than for the constant-stress case, which may be appropriate for discussing the flow induced by the surface motion of plates.The relatively small depth gradient of viscosity, for constant strain rate, suggests that the lower mantle could also participate in convection. The effective viscosity increases with depth, however, by at least 102 to 103 from the top to the bottom of the lower mantle, for a reasonable range of activation volumes and temperatures. There will be a low-viscosity layer at the base of the mantle, in contrast to the high-viscosity layer at the top of the mantle (plates), if a thermal boundary layer is present. The constant Newtonian viscosity inferred from rebound data may be an apparent feature resulting from the difference in deformation mechanisms between isostatic rebound and large-scale flow.  相似文献   

17.
磷是地表水体中的关键性营养盐,在水生生态系统的物质循环与能量流动方面发挥着重要作用,研究水体中磷的来源、转化与归趋对于了解水环境的演变过程与科学保护具有重要意义.近年来,磷酸盐氧同位素(δ18 O P)技术已逐渐应用于淡水环境中磷的来源示踪与生物地球化学循环研究,其样品前处理主要沿用海水方法体系.相比而言,淡水样品中PO 3-4浓度通常较低,有机质和干扰离子含量却较高,复杂的样品前处理过程极大地制约了δ18 O P分析在淡水环境体系的广泛应用.为此,本研究针对现有海水样品δ18 O P前处理方法在地表淡水环境的适用性加以检验,并进行了三点优化改进:①将MAGIC沉淀步骤使用的MgCl 2替换为Mg(NO 3)2,避免了Cl-的干扰,减少AgCl杂质的生成;②调节生成Ag3PO4溶液pH值为8.0,保证Ag3PO4沉淀快速完全;③对Ag3PO4沉淀过程采用避光处理,降低了AgNO 3及Ag3PO4可能的光解影响,提高了Ag3PO4的纯度,使δ18 O P的测试结果更为准确.本改进方法为后续利用δ18 O P技术深入探究淡水环境中磷的生物地球化学循环与生态环境效应提供了有益的方法借鉴.  相似文献   

18.
Lacustrine groundwater discharge (LGD) and the related water residence time are crucial parameters for quantifying lake matter budgets and assessing its vulnerability to contaminant input. Our approach utilizes the stable isotopes of water (δ18O, δ2H) and the radioisotope radon (222Rn) for determining long‐term average and short‐term snapshots in LGD. We conducted isotope balances for the 0.5‐km2 Lake Ammelshainer See (Germany) based on measurements of lake isotope inventories and groundwater composition accompanied by good quality and comprehensive long‐term meteorological and isotopic data (precipitation) from nearby monitoring stations. The results from the steady‐state annual isotope balances that rely on only two sampling campaigns are consistent for both δ18O and δ2H and suggested an overall long‐term average LGD rate that was used to infer the water residence time of the lake. These findings were supported by the good agreement of the simulated LGD‐driven annual cycles of δ18O and δ2H lake inventories with the observed lake isotope inventories. However, radon mass balances revealed lower values that might be the result of seasonal LGD variability. For obtaining further insights into possible seasonal variability of groundwater–lake interaction, stable water isotope and radon mass balances could be conducted more frequently (e.g., monthly) in order to use the derived groundwater discharge rates as input for time‐variant isotope balances.  相似文献   

19.
湖南宁乡钾镁煌斑岩是寻找湖南原生金刚石矿床的重要线索之一。本文通过对宁乡V号煌斑岩岩管岩石地球化学的分析及其与其它地区钾镁煌斑岩的对比,确定宁乡V号岩管煌斑岩与前人所研究的宁乡钾镁煌斑岩特征基本一致。但与西澳典型含金刚石的钾镁煌斑岩相比,其SiO2、Al2O3、MnO的含量较高,MgO、TiO2、K2O含量较低,这可能与钾镁煌斑岩的岩浆来源及演化过程有关,显示其地幔源区来源相对于西澳钾镁煌斑岩的源区较为富集。  相似文献   

20.
矿产远景地质调查过程中,在江西华齐铜多金属矿区发现含矿硅质岩。测试分析显示,区内硅质岩贫A l2O3、T iO2,Co、C r等元素含量低,贫ΣREE,δ（Eu）为负异常,δ（C e）为弱正异常,HREE相对富集等热水沉积物的特征。在判别硅质岩形成的系列图解上,样品均指示热水沉积作用和大陆边缘环境,这与S iO2/A l2O3、S iO2/（K2O＋N a2O）、S iO2/M gO、M nO/T iO2、K/R b等特征值所指示的结果相一致。本区硅质岩地球化学特征及其对比结果说明该区域构造演化的复杂性。在元古代华南海槽构造演化中在华夏地块边缘发生断裂拉张,形成断陷盆地,并发生了热水喷流沉积成岩成矿作用。本区硅质岩与成矿关系密切,研究硅质岩对于认识区域构造演化及寻找矿化体具有重要意义。  相似文献   

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