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1.
Si-Fe-Mn-oxyhydroxides dredged at the PACMANUS(Papua New Guinea–Australia–Canada–Manus)hydrothermal field, Eastern Manus Basin, have 87Sr/86Sr=0.708 079–0.708 581; εNd=5.149 833–6.534 826;208Pb/204Pb=38.245–38.440; 207Pb/204Pb=15.503–15.560; 206Pb/204Pb=18.682–18.783. 87Sr/86 Sr isotope ratios are relatively homogeneous and close to the value of the surrounding seawater(0.709 16). The content of Sr in the samples contributed by seawater was estimated to be 76.7%–83.1% of total amount. The mixing temperature of hydrothermal fluids and seawater were ranging from 53.2°C to 72.2°C and the hydrothermal activities were unstable when the samples precipitated. The εNd values of all the samples are positive, which differ from the values of ferromanganese nodules(crusts) with hydrogenic origin. Nd was mainly derived from substrate rocks leached by hydrothermal circulation and preserved the hydrothermal signature. Pb isotopic compositions of most samples show minor variability except Sample #9–2 that has relatively high values of Pb isotopes. The Pb may be derived from the Eastern Manus Basin rocks leached by the hydrothermal fluid. The slightly lower 208Pb/204 Pb and207Pb/204 Pb values of the samples indicated that the hydrothermal circulation in PACMANUS was not entire and sufficient, or that hydrothermal circulation had transient changes in the past. Si-Fe-Mn-oxyhydroxides in the samples preserved the heterogeneities of local rocks.  相似文献   

2.
The formation mechanism of the large hydrothermal sulˉde deposit is a complex geological process involving many controlling factors. Mixing between hydrothermal °uid and seawater plays a key role in this process. The results of the Ocean Drilling Program (ODP) indicate that mixing of the evolved seawater and hydrothermal °uid, which is wildly developed within the Trans-Atlantic Geo- Traverse (TAG) hydrothermal deposit, governs the internal structure and chemical compositions of the deposit to great extent. Taking the TAG ˉeld for example, the mixing processes of hydrothermal °uid with the seawater heated to di?erent extent are calculated, so as to discuss the impact of hydrothermal °uid/seawater mixing on the formation process of the sulˉde deposit. The results indicate that: (1) mixing between the heated seawater and hydrothermal °uid derived from the deep deposit is largely responsible for the wild precipitation of anhydrite within the TAG hydrothermal deposit; (2) 330{310 ±C is a special temperature range in the mixing process; (3) the mixing and hydrothermal processes in di?erent zones of the TAG hydrothermal deposit (TAG-1, TAG-2 and TAG-5, etc.) have been discussed based on the simulated results.  相似文献   

3.
The major elements, rare earth elements （REE） and trace elements of four basalt samples from central and western Pacific ferro- manganese crust provinces have been analyzed using chemical methods and ICP - MS, respectively. The results indicate that the samples have been extensively altered and that the contents of their major elements have changed significantly. However, the similarity of REE partition patterns and trace element contents of basalt samples to those of fresh oceanic island basalts （OIB） indicate that the basalt samples originated as OIB. Because of low-temperature alteration, the contents of A1203 , Fe203 , MnO, K20 and P205 increased, while MgO and FeO decreased. Active components, such as magnesium and iron, were leached from OIB resulting in the relative enrichment of SiO2. The leaching of active components can cause the relative enrichment of REE, while the precipitation of LREE-rich ferromanganese oxides in vesicles and fissures not only causes an increase of REE contents, but also induces ＂fractionation＂ of LREE and HREE. Based on the enrichment mechanism of REE contents, the theoretical quantities of precipitated ferromanganese oxides and the depleted quantities of active components are calculated ： the depleted quantities of active components for the unit mass of fresh basalts vary in the range of 0.15 ～ 0. 657, and the precipitated quantities of ferromanganese oxides for the unit mass of fresh basahs vary in the range of 0. 006 ～ 0. 042. Of the major elements, the two most depleted are iron, and magnesium, with 18.28% ～ 70.95% of iron and 44.50% ～ 93.94% of magnesium in the fresh basalts was leached out. Theoretical calculation and geochemistry results both indicate that low-temperature alteration of basalts can supply abundant amount of metals to seawater, and may play an important role in ocean metal circulation.  相似文献   

4.
This study reports the occurrence of anhydrite in hydrothermally altered pillow basalt (12°50.55′N, 103°57.62′W, water depth 2 480 m), which may have been produced in the basalt during seawater-basalt interaction in the laboratory. The existence of anhydrite in the altered basalt indicates extensive hightemperature hydrothermal alteration at the surface of seafloor pillow basalt. Microprobe analysis shows significant chemical zoning in the hydrothermally altered pillow basalt, in which Ca, Si and Al contents decrease and P, Fe, Mn, Cr and S contents increase from fresh basalt to altered basalt. The negative correlation between Rb-Sr and Li-Sr, and negative correlation between Li-Ca and Rb-Ca in the high-temperature vent fluids show that these fluids underwent anhydrite precipitation before fluid jetting due to mixing with seawater in the sub-seafloor. Based on these observations, we show that not all Ca in the anhydrite comes from basalt in the reaction zone, and that the basalts on the seafloor or in the upflow zone may also provide Ca for anhydrite.  相似文献   

5.
To understand the source and nature of the ore-forming fluids of the Edmond hydrothermal field on the Central Indian Ridge, we studied the He-Ar isotope composition and fluid inclusions of the hydrothermal precipitates.Our results show that the sulfide samples contain noble gases He, Ne, Kr, and Xe with their abundances in between those of air-saturated water(ASW) and mid-ocean ridge basalt(MORB). The ~3He/~4He ratio varies from1.3 to 8.7 R_a(n=10, average: 5.1 R_a), whereas the ~(40)Ar/~(36) Ar ratio is from 285.3 to 314.7(n=10, average: 294.8). These results suggest that the He was derived from a mixture of MORB with variable amounts of seawater, but the Ar in the ore-forming fluids trapped in the sulfides is predominantly derived from seawater. The fluid inclusions of barite have a wide range of homogenization temperatures and salinities varying from 163°C to 260°C and 2.6 wt%to 8.5 wt% Na Cl equiv., respectively. It is suggested that the ore-forming fluids were produced by phase separation, which agreed with the present-day vent fluid study.  相似文献   

6.
Polymetallic sulfides from two hydrothermal chimneys and talus deposit from the Vienna Woods field of Manus Basin were studied for mineralogy, elemental composition, and S-isotope ratio to understand their evolution. The factors including the nature of source fluid, mineral paragenesis, and related geochemical processes have been discussed. Mineralogy and elemental concentration of Cu and Fe-rich large chimney at the central part of this hydrothermal field was completely different from the smaller Zn-rich peripheral chimney and Fe-rich talus deposit, suggesting the variable degree of alterations generate physico-chemically different source fluids responsible for these hydrothermal structures. Similarly, S-isotope ratios also indicate chemically diverse fluids and different modes of precipitation were involved in their evolution. Distinct mineral zonings and associated elemental and isotopic compositions within individual deposit confirm paragenetic shifts were involved during their growth process.  相似文献   

7.
In sediments of the Central Pacific, water depth is the controlling factor of the distribution of Si, Al, Fe and CaCO, .In the shallow and subabysmal areas, CaCO3 content is much greater than that in the abysmal areas where Si, Al and Fe contents are much lower than those in shallow and subabysmal areas. The contents of Si, Al, and Fe increase and that of CaCO3 decrease with the variation of grain size of sediments from coarse to fine. The contents of Al, Si, and Fe are positively related to each other and the content of CaCO3 is negatively related to that of the three elements. The evident regularities of the distribution of Si, Al, Fe and CaCO, in the sediments have revealed to a certain extent that they may be used as the environmental indicators in some cases.  相似文献   

8.
-The i. r. spectra of Na4 [UO2 (CO3)3], Na [UO2 (OH)3] and the surface species of uranium on HTO underthe condition of flowing natural seawater and concentrated seawater (NaCl-NaHCO3-U) were recorded, with the bands of urany! of surface species obtained and the finding that iigands of surface species besides HTO are mainly water and OH, and there are some CO32- groups under the condition of natural seawater. Some relations between the complex properties and the j. r. spectroscopic characters for uranyl complexes were studied, and the transferred change quantity of surface complex was calculated.Structure models for surface species of adsorption are herein presented and the mechanism for uranium adsorption is deduced.  相似文献   

9.
A 43 cm long E271 sediment core collected near the East Pacific Rise(EPR) at 13°N were studied to investigate the origin of smectite for understanding better the geochemical behavior of hydrothermal material after deposition.E271 sediments are typical metalliferous sediments. After removal of organic matter, carbonate, biogenic opal,and Fe-Mn oxide by a series of chemical procedures, clay minerals(2 μm) were investigated by X-ray diffraction,chemical analysis and Si isotope analysis. Due to the influence of seafloor hydrothermal activity and close to continent, the sources of clay minerals are complex. Illite, chlorite and kaolinite are suggested to be transported from either North or Central America by rivers or winds, but smectite is authigenic. It is enriched in iron, and its contents are highest in clay minerals. Data show that smectite is most likely formed by the reaction of hydrothermal Fe-oxyhydroxide with silica and seawater in metalliferous sediments. The Si that participates in this reaction may be derived from siliceous microfossils(diatoms or radiolarians), hydrothermal fluids, or detrital mineral phases. And their δ30 Si values are higher than those of authigenic smectites, which implies that a Si isotope fractionation occurs during the formation because of the selective absorption of light Si isotopes onto Feoxyhydroxides. Sm/Fe mass ratios(a proxy for overall REE/Fe ratio) in E271 clay minerals are lower than those in metalliferous sediments, as well as distal hydrothermal plume particles and terrigenous clay minerals. This result suggests that some REE are lost during the smectite formation, perhaps because their large ionic radii of REE scavenged by Fe-oxyhydroxides preclude substitution in either tetrahedral or octahedral lattice sites of this mineral structure, which decreases the value of metalliferous sediments as a potential resource for REE.  相似文献   

10.
A seafloor hydrothermal field, named Deyin-1 later, near 15°S southern Mid-Atlantic Ridge(SMAR) was newly found during the 22 nd cruise carried out by the China Ocean Mineral Resources Research Development Association(COMRA). Sulfide samples were collected at three stations from the hydrothermal field during the26 th cruise in 2012. In this paper, mineralogical characteristics of the sulfides were analyzed with optical microscope, X-ray diffractometer, scanning electron microscope and electron microprobe to study the crystallization sequence of minerals and the process of hydrothermal mineralization. According to the difference of the ore-forming metal elements, the sulfide samples can be divided into three types:(1) the Ferich sulfide, which contains mainly pyrite and chalcopyrite;(2) the Fe-Cu-rich sulfide consisting predominantly of pyrite, chalcopyrite and isocubanite, with lesser amount of sphalerite, marmatite and pyrrhotine; and(3) the Fe-Zn-rich sulfide dominated by pyrite, sphalerite and marmatite, with variable amounts of chalcopyrite, isocubanite, pyrrhotine, marcasite, galena and gratonite. Mineral precipitations in these sulfides are in the sequence of chalcopyrite(isocubanite and possible coarse pyrite), fine pyrite,sphalerite(marmatite), galena, gratonite and then the minerals out of the dissolution. Two morphologically distinct generations(Py-I and Py-II) of pyrite are identified in each of the samples; inclusions of marmatite tend to exist in the coarse pyrite crystals(Py-I). Sphalerite in the Fe-Zn-rich sulfide is characterized by a"chalcopyrite disease" phenomenon. Mineral paragenetic relationships and a wide range of chemical compositions suggest that the environment of hydrothermal mineralization was largely changing. By comparison, the Fe-rich sulfide was formed in a relatively stable environment with a high temperature, but the conditions for the formation of the Fe-Cu-rich sulfide were variable. The Fe-Zn-rich sulfide was precipitated during the hydrothermal venting at relatively low temperature.  相似文献   

11.
Marine hydrogenetically precipitated ferromanganese crusts are widespread in the Pacific Ocean. They occur as pavements coating volcanic or sedimentary hard-rock substrates, mainly on the slopes of seamounts, plateaus and hills in ocean basins and continental margins. We studied three ferromanganese crusts from one dredge haul from the Rivera Plate (western margin of Mexico), which are up to 15 mm thick and grow directly on a substrate of pillow basalt fragments. They consist of laminated, botryoidal, porous aggregates mostly of Fe and Mn oxyhydroxides and up to 10% silicates. XRD analysis showed the predominance of poorly crystallized mineral phases in the crusts that include Mn-feroxyhyte and vernadite, and an authigenic smectite-like clay. Detrital minerals probably derive from granodiorites of the eastern wall of the neighboring Middle America Trench. Scattered barite grains occur on the crust surface and suggest plume fall-out derived from hydrothermal vents, although a possible pelagic source cannot be dismissed. Ratios between major (Fe, Mn, Si) and trace (Co, Ni, Cu) elements reveal that such crusts are predominantly hydrogenetic in origin, although they show a hydrothermal influence that increases in the outer layers. Iron contents range from 16.2 to 25.2 wt.%, and manganese from 3.4 to 14.5 wt.%. The Fe/Mn ratio ranges from 1.6 to 7.0. The SiO2/Al2O3 ratio ranges from 4.3 to 6.6, indicating the presence of biogenic silica (radiolarians). The concentrations of copper (up to 383 ppm) and cobalt (up to 534 ppm) are significantly below those of the typical hydrogenetic crusts, whereas Ni (up to 1320 ppm) is about the same or slightly lower. REE normalized profiles and ΣREE values (486 to 732 ppm) match those reported for hydrogenetic crusts, but suggest a hydrothermal contribution for the later crust layers. The inferred crust growth rates using the Co-chronometer (44 and 229 mm/Myr) are higher than those reported for pure hydrogenetic crusts (mostly 1 to 6 mm/Myr), thus indicating an increasing hydrothermal influence. The highest growth rate (229 mm/Myr, corresponding to the outer crust layers) suggests a regional hydrothermal input of iron and manganese to seawater. The intensification of regional submarine hydrothermal activity began about 13,000 yr ago, and may be related to the tectonic activity in the complex junction of the Rivera, Cocos, Pacific and North America plates.  相似文献   

12.
用化学方法和ICP-MS方法分别对中、西太平洋海山富钴铁锰结壳产出区玄武岩的主元素、微量元素和稀土元素(REE)含量进行了测定,结果表明,研究区玄武岩经受了强烈的洋底低温蚀变作用,主元素成分发生了明显的变化,失去了原岩的特征.样品与新鲜大洋岛屿玄武岩(OIB)极为相似的稀土元素配分模式和微量元素含量特征表明,所研究的岩石属典型的大洋板内玄武岩.受洋底低温蚀变作用的影响,样品的Al2O3,Fe2O3,MnO、K2O,P2O5含量增加,MgO,FeO的含量降低.蚀变作用使大洋岛屿玄武岩中的镁、铁等活动组分大量流失,从而表现出相对富SiO2的特征(标准矿物计算结果中出现石英).由于蚀变作用,活动组分的流失使样品的REE相对富集,而富REE铁锰氧化物在玄武岩气孔和裂隙中的沉淀不仅使样品的REE含量增大,而且引起轻稀土元素(LREE)与重稀土元素(HREE)分馏,表现为∑c(Ce)/∑c(Yb)值增大.以REE富集机制为基础,对样品中铁锰氧化物的沉淀量和单位质量新鲜玄武岩中活动组分的流失量进行了理论计算,结果表明,因低温蚀变作用所引起的新鲜玄武岩的单位质量亏损为0.150~0.657,而单位质量新鲜玄武岩中铁锰氧化物的沉淀量为0.006~0.042.主元素中以铁、镁的流失亏损最为明显,新鲜玄武岩中铁、镁的流失比例分别为18.28%~70.95%和44.50%~93.94%,超过了岩石总量的流失亏损比例(15.0%~65.7%),因而样品相对贫铁、镁.其他元素的流失量和流失比例都很好地印证了地球化学研究的结果.样品中铝、钾、磷负的流失量是由于沸石在岩石气孔中的充填和岩石的磷酸盐化.理论计算结果和地球化学研究都表明,大洋岛屿玄武岩的低温蚀变向海水提供了大量金属,这是大洋海水中金属循环的重要环节.  相似文献   

13.
本文针对采自印度洋深海中最常见的两类生物成因沉积物——钙质软泥和硅质软泥，开展了全岩样和不同粒级组分中常微量元素、稀土元素和Y（REY）含量的系统分析，探讨了两类沉积物中REY的组成特征、物质来源和富集机制。研究表明，钙质软泥以富含CaO和Sr为主要特征，硅质软泥则富集SiO2、Al2O3、Fe2O3等。钙质软泥中∑REY平均含量为40.56×10-6，轻稀土元素（LREE）略有富集，REY有向细粒沉积物中富集的特征，PAAS标准化后全岩样和不同粒级组分均表现为Ce负异常、Eu和Y正异常；REY以自生来源为主，继承了海水的组成特征，同时也受到了热液流体物质和洋底玄武岩风化产物的影响。硅质软泥中∑REY的含量为248.54×10-6，LREE相对富集，REY在4φ以细的沉积物中富集；研究站位沉积物中∑REY含量处于边界品位附近，但在细粒级沉积物中重稀土元素（HREY）含量则达到了工业品位；该类沉积物细粒组分中REY主要来自陆源或火山碎屑组分中黏土矿物和铁锰氧化物吸附作用，粗粒组分中REY来源则主要与生物作用相关；硅质软泥中REY的富集与沉积物中磷灰石等矿物相关，部分不同来源的REY可能是在沉积之后的成岩过程中再次分配向磷灰石、钙十字沸石等矿物中富集。  相似文献   

14.
Fe-Si oxide deposits were recovered from the PACMANUS (Papua New Guinea-Australia-Canada-Manus) hydrothermal field in Eastern Manus basin. Samples were loose and fragile. Optical and scanning electron microscopy showed that the samples had abundant rod-like or twisted filamentous and granular structures. Electron probe microanalysis revealed that these filaments and grains were mainly composed of Fe and Si. The presence of spherical grains on the surface of the filaments suggests the intergrowth of biotic and abiotic reactions. Biotic and abiotic kinetics competition always exists in the redox gradient. Based on the physico-chemical conditions of PACMANUS hydrothermal fluids, we calculated a strict abiotic oxidation rate of Fe2+ to Fe3+, which is approximately 0.0123 g/min. If the fluids had been erupting consistently and the concentration of Fe2+ was constant, 3.232 kg per year of Fe would be deposited in this vent. The amount of Fe oxides around the studied vent was larger than the amount determined by strict abiotic kinetic calculation. Bacteria may also play an important role in Fe oxidation. A mesh-like microenvironment constructed by biogenic filaments ensured adequate Fe2+ and low oxygen content for the growth of bacteria. Moreover, this structure promoted the deposition of abiotic Fe-Si oxides.  相似文献   

15.
Pore water chemistry (total dissolved CO2, NH4, NO3, NO2, PO4, Si(OH)4, Ca, Mg, Fe, Mn, SO4, H2S and F, and titration alkalinity), solid phase chemistry (Corg, Porg, CTOT, NTOT, F, SiOPAL and SII), and sediment characteristics (porosity, dry bulk density and formation factors) were determined on a centimeter-scale spacing in the upper 20–40 cm of sediments under intense upwelling areas on the Peru continental shelf. These data demonstrate that carbonate fluorapatite (CFA) is precipitating from pore waters in the upper few centimeters of a gelatinous mud with high organic carbon content (up to 20% Corg), very high porosity ( > 0.96 ml cm−3) and very low dry bulk density (< 0.1 g cm−3). Dissolved phosphate concentrations at the sediment-water interface range from 20 to 100 μM, orders of magnitude higher than bottom-water concentrations, and much higher than predicted from regeneration of organic matter. The mechanism of this interfacial phosphate release is unclear, but is apparently uncoupled from carbon and nitrogen metabolism and thus may be linked either to dissolution of fish debris or to the presence of a microbial mat in surficial sediments. Fluoride is incorporated into CFA by diffusion from the overlying seawater, and carbonate ions are provided from pore-water alkalinity. Magnesium concentrations in this reaction zone are not significantly different from those of seawater, suggesting that magnesium depletion is not a necessary prerequisite for CFA precipitation.

The environment of precipitation is interface-linked rather than driven by organic diagenesis of phosphorus deeper in the sediment. Most of the cores display a wide range of diagenetic characteristics below the immediate interfacial region, but almost all show the precipitation signature near the interface. This interface-linked early diagenetic porewater environment for the precipitation of CFA explains many of the geochemical characteristics of phosphorites and provides a “testable” model to compare the modern phosphogenic analog with ancient phosphorite deposits. Two of the cores display very high solid phase phosphorus and fluoride contents reflecting the presence of apparently modern pelletal apatites.  相似文献   


16.
对大洋27航次在西太平洋马里亚纳海沟挑战者深渊获取的3个多金属氧化物样品进行了X射线矿物衍射分析、穆斯堡尔谱分析及地球化学元素分析,研究其矿物、地球化学特征差异。结果表明,所取样品处于多金属氧化物发育的初始阶段,具有独特的矿物地球化学特征:(1)相较于太平洋CC区及中太平洋海盆获取的多金属结核样品,本研究样品的矿物组成中含有异常高的石英、斜长石以及黏土矿物,而水羟锰矿和钙锰矿含量较低。(2)样品中铁相矿物主要为正方针铁矿(91.6%),另含少量纤铁矿(8.4%),推测是纤铁矿向更加稳定的正方针铁矿衍变的结果。(3)由于样品中深海黏土组分以及氧化物核心物质的混入,加上吸附金属氧化物时间较短,导致SiO2和Al2O3含量均高于正常结核,而Fe、Mn、Cu、Co、Ni等其余金属元素含量较低。(4)由于形成时间较短,样品中稀土元素含量相对较低,ΣREE仅约为0.4×10-3(一般太平洋CC区及中太平洋结核中稀土含量均大于1.0×10-3);加之海水氧化还原作用的降低以及研究区海底热液活动的影响,Ce元素未表现出多金属结核中常见的正异常。  相似文献   

17.
河口活性硅酸盐除了被稀释和被吸收外,有没有进行明显的无机化学转移?一直到最近几年,仍然是国际上争论的问题[1-6]。我们已在本研究第Ⅰ篇[1]报导了河口活性硅含量分布;河水与无硅海水人工混合后活性硅含量变化;电解质浓度和pH值对硅酸盐溶液中活性硅含量的影响以及吸附剂影响的初步实验;证实了河水和海水混合后活性硅含量的变化主要决定于悬浮物、电解质、pH值三个因素的同时作用。  相似文献   

18.
Pulleniatina obliquiloculata shells from 16 core-top samples from the tropical Indo-Pacific Oceans are analyzed for the ratios of boron and cadmium to calcium(B/Ca and Cd/Ca). The B/Ca ratios show a very weak positive relationship with [B(OH)_4~-] and the dissolved carbonate species at the apparent calcification depth of P.obliquiloculata. The boron partition coefficients(K_D) between P. obliquiloculata B/Ca and seawater[B(OH)_4~-]/[HCO_3~-] distribute around 1.1×10~(-3)-1.3×10~(-3) with a mean value of(1.19±0.12)×10~(-3),and are significantly related to the nutrient concentration, especially phosphate. The lack of any clear correlation between the P. obliquiloculata B/Ca and seawater carbonate chemical parameters suggests that the physiochemical controls on boron incorporation are masked by the complexity of natural seawater condition. But the significant dependence of Ku on nutrient may likely be explained by a nutrient related growth-rate effect. Cd/Ca of P.obliquiloculata shows significant correlation with seawater phosphate concentration, and its partition coefficients(D_(cd)) are significantly related to temperature. A first-principle methodology of P. obliquiloculata B/Ca is applied;with the aid of Cd/Ca as a phosphate proxy and a constraint on K_D, to estimating sea water carbonate chemistry(e.g., pH). The results are fairly promising and allow us to propose the possibility to apply the combination of B/Ca and Cd/Ca proxies(and also Mg/Ca and δ~(18)O for estimating temperature and salinity) for the paleoreconstruction of seawater carbonate chemistry.  相似文献   

19.
The results of geochemical studies of particulate matter in the water mass over the hydrothermal field at 9°50′ N on the East Pacific Rise are presented. The particulate matter was tested in background waters, in the buoyant plume, and in the near-bottom waters. The contents of Si, Al, P, Corg, Fe, Mn, Cu, Zn, Ni, Co, As, Cr, Cd, Pb, Ag, and Hg were determined. No definite correlations were found between the ele-ments in the background waters. Many of the chemical elements correlated with Fe and associated with its oxyhydroxides in the buoyant plume. In the near-bottom waters, microelements are associated with Fe, Zn, and Cu (probably, to their sulfides formed under fluid mixing with seawater). The matter precipitated in a sed-imentation trap was similar to the near-bottom particulate matter in the elemental composition.  相似文献   

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