首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
For the past ten years much work has been carried out on clay minerals of volcanic ash soils. Most investigators have reported that allophane is dominant among clay minerals of volcanic ash soils and crystallizes to halloysite or meta-halloysite with the advance of weathering (1–8). On the other hand, UCHIYAMA, MASUI and ONIKURA (1960) found that montmorillonite predominates in the clay fraction of volcanic ash soil in Kawatabi (9). Furthermore, MASUI, SHOJI and UCHIYAMA (1966) showed that the major crystalline clay minerals of volcanic ash soils in the Tohoku district are montmorillonite, vermiculite, intergradient montmorillonite-vermiculite and chlorite (10). They also showed that these minerals increase with the advance of weathering and that kaolin minerals are minor constituents.  相似文献   

2.
A contrasting occurrence of clay minerals was found within a soil profile which was derived from volcanic materials in the suburbs of Fukuoka-city, Northern Kyushu. The soil profile is located on an isolated terrace, and the morphological characteristics of the soil correspond exactly to Andosols, so-called Kuroboku soils or Humic Allophane soils.

The clay fraction of upper horizons of the soil consists largely of alumina-rich gel-like materials, gibbsite, and layer silicates such as chlorite and chloritevermiculite intergrades, while that of lower horizons is composed of allophane and gibbsite or halloysite. There was no positive indication of allophane in the upper horizons. Corresponding with the clay mineralogical composition, quartz is abundant in the fine sand fraction of the upper horizons, while the mineral is very scarce or none in the lower horizons, suggesting a close relation between the petrological nature of parent volcanic materials and the mineralogical composition of weathering products. The dominant clay mineral in the volcanic 1.10il might be dependent on the petrological nature of parent materials, and allophane is mostly formed from andesitic materials, and alumina-rich gel-like materials and layer silicates have come from quartz andesitic materials. Allophane would transform to gibbsite or halloysite according to weathering conditions, and aluminarich gel-like materials change to gibbsite under a well-drained condition.

The soil materials have been so greatly weathered that some horizons contain gibbsite of even more than 40 per cent or halloysite over 70 per cent. The morphology and mineralogy are quite similar to so-cailed “non-volcanic Kuroboku soils.”  相似文献   

3.
The soils of Rajasthan vary from desert sand to heavy clay with all intermediate stages like sandy loam, loam and clay loam. The last two textural groups are more prevalant on the eastern, northeastern and southeastern part of the Aravallies which run almost in the middle of the State from southeast to northeast. The latter groups of soils have more potential from the point of agricultural development in the State. These soils are widely termed as alluvial soils which is a general term to indicate the nontaxonomic group of soils that have parent material of alluvial origin, Riecken 17, Kelloog 8 has referred to the soils developed from the alluvium as classified under variety of world soil groups. In our country many of the alluvial soils have not yet been studied from the soil genesis point of view as a measure to classify the soils under taxonomic groups. Ray Chawdhary and Mukerji 15, concluded that the alluvial soil groups of our country are ill defined and the classification of these soils need more study. Basu 3 was able to distinguish the genetic characteristics of the soils of Deccan. Agrawal and Mukherji 1) established that distinct genetic soil types have come into expression under Gangetic alluvium. Agarwal 2 has concluded about the three types of soils in the toposequence with precipitated calcium throughout, zone of calcium accumulation in the bottom of the profile and soils free of calcium, and suggests that the soils of Gangetic plain be called as derived from alluvium. A process of reclassifying the alluvial soil series into taxonomic groups is a common trend in the United States since the last two decades.  相似文献   

4.
Phosphorus in soils is found to be present in organic combinations, inorganic form or in adsorted form on clay complex. Different forms of soil phosphorus have different solubilities and consequent availability in soils. A knowledge about the content and types of soil phosphorus enables one to understand the organic behaviour and predict the response of added phosphatic material to crops (Parker 1953). The form in which phosphorus is present in soil is directly related to pH and CaCO3 in the soil as well as the intensity of the development of the soil. Williams (1950) has found that in calcareous soils of South Australja most of the phosphorus was in combination with calcium, whereas in acid soils it forms compounds with alumina and iron. Hibbard (1931) concluded that in alkaline and calcareous soils, phosphorus exists mostly in the form of hydroxyapatite, chloroapatite, and the like. Kanwar and Grewal (1959) studied fractionation of phosphorus in Punjab soils and reported that differences in the nature and amounts of the phosphorus present in acid and alkaline soils of the State explain the causes of different phosphatic fertilizer responses to the crops. A similar report has been given by Goel and Agarwal (1959) who studied the fractionation of phosphorus in Kanpur soils and concluded that the mature soils are rich in iron and aluminium bound phosphorus and respond better to phosphatic fertilizer than the immature soils rich in Ca2+ and Mg2+ bound phosphorus. Chai Moo Cnoo and Caldwell (1959) reported that Fe3+ and Al3+ bound phosphorus was abundant in acid soils while Ca2+ and Mg2+ bound phosphorus content in alkaline soils, and organic phosphorus agreed, in general, with the content of organic matter, with some deviations.  相似文献   

5.
Allophane has been known to occur widely in volcanic ash soils in Japan and New Zealand. However, exact knowledge of its nature has not been well established, mainly because of extreme difficulty to separate it in pure state and of its x-amorphous nature. In the course of the studies on soil allophane, it was noticed that certain Ando soils contained two different mineral colloids together, in addition to crystalline clay minerals and free sesquioxides. X-ray examination revealed that one was x-amorphous colloid which would be called allophane, and the other an unknown colloid of low crystallinity. Imogolite*** Imogolite will be described in a subsequent paper by the present authors. was proposed as the name of the latter colloid by the present authors after imogo in which imogolite was first found. Imogo is a brownish yellow, volcanic ash soil. in the Kuma basin in the Kumamoto Prefecture3). When deferration treatment is applied to the soils, allophane disperses both in an acid and alkaline media, whereas imogolite disperses in an acid medium and flocculates in an alkaline one.  相似文献   

6.
In the past several years, the occurrence of vermiculite-type clay minerals and the problem of the formation of Al-interlayers have attracted the intensive attention of soil clay mineralogists. A number of papers have appeared in Japan, in Which the identification data of the vermiculite-type minerals with stable 14 Å spacing were given. (Matsui 1959, 1960; Kanno 1961b, Kato 1961, 1962a, 1962b; Egawa 1963).  相似文献   

7.

Purpose

Information on the physicochemical properties, mineral species and micromorphology of lateritic soils and gravel soil layers in paleo-environmental soil profile is severely lacking. Red soil profile of the Taoyuan terrace was employed to demonstrate its different extents of lateritic weathering. The objectives of this study were to compare the physicochemical properties of lateritic soils and gravel soil layers and identify using conventional and synchrotron X-ray diffraction (XRD) analyses mineral species in nanoparticles separated by automated ultrafiltration device (AUD) apparatus.

Materials and methods

Soil samples were collected from paleo-environmental lateritic soils. Soil samples were examined using elemental analysis, conventional and synchrotron XRD analyses, high gradient magnetic separation, separation and collection of nanoparticles by AUD apparatus, and transmission electron microscopy (TEM).

Results and discussion

The soil pH, redness index, quantities of free Al- and Fe-oxides (Ald and Fed), and clay content of lateritic soils are higher than those of gravel soil layers. Illite, kaolinite, gibbsite, quartz, goethite, and hematite were identified in clay fractions and nanoparticles by conventional and synchrotron XRD analyses. TEM images show presence of hematite nanoparticles on the surface coating of kaolinite nanoparticles and aggregated hematite nanoparticles overlapping the edge of a kaolinite flake in a size range of 4?C7?nm. Synchrotron XRD techniques are more straightforward and powerful than conventional XRD with random powder methods for identifying nanoparticles in red soils, particularly for illite, kaolinite, goethite, and hematite nanoparticles. According to chemical compositions of clay fractions and red soil features in the Taoyuan terrace, these red soils can be taken as lateritic red earths or red earths.

Conclusions

This work suggests that physicochemical properties, mineral species, and micromorphology of red soil at all depths can shed light on the extent of paleo-environmental lateritic weathering.  相似文献   

8.
One of the authors, Kumada(1), has presented the idea that humification must be regarded as browning phenomena of organic matter in soils. The browning reaction can be accelerated non-enzymatically as well as enzymatically, and it is considered that humification would be conducted under the influence of some catalytic actions of clay fraction, composed of various kinds of clay minerals, free oxides and electrolytes, as well as soil enzymes, under the prevailing hydrothermal conditions. This was well illustrated by Kyuma and Kawaguchi(2), who definitely demonstrated the catalytic effect of allophane on the oxidative polymerization of polyphenols.  相似文献   

9.
The clay minerals of more than 200 soil samples collected from various sites of Fujian Province were studied by the X-ray diffraction method and transmission electron microscopy to study their distribution and evolution.Montmorillonite was found in coastal solonchak,paddy soils derived from marine deposit,lacustrine deposit and river deposit,and some lateritic red soil,red soil and yellow soil with a low weathering degree.Chlorite existed mainly in coastal solonchak and paddy soil developed from marine deposit.1.4nm intergradient mineral appeared frequently in yellow soil,red soil and lateritic red soil.The content of 1.4nm intergradient mineral increased with the decrease of weathering degree from lateritic red soil to red soil to yellow soil.Hydrous micas were more in coastal solonchak,paddy soils derived from marine deposit,lacustrine deposit and river deposit.and puple soil from purple shale than in other soils.Kaolinte was the most important clay mineral in the soils iun this province.The higher the soil weathering degree,the more the kaolinite existed.From yellow soil to red soil to lateritic red soil,kaolinite increased gradually,Kaolinite was the predominant clay mineral accompanied by few other minerals in typical lateritic red soil. Tubular halloysite was a widespread clay mineral in soils of Fujian Province with varying quantities.The soil derived from the paent rocks rich in feldspar contained more tubular halloysite.Spheroidal halloysite was found in a red soil and a paddy soil developed from olivine basalt gibbsite in the soils in this district was largely“primary gibbsite” which formed in the early weathering stage.Gibbsite decreased with the increase of weathering degree from yellow soil to red soil to lateritic red soil.Goethite also decreased in the same sequence while hematite increased.  相似文献   

10.
Published information, both theoretical and experimental, on As chemical behavior in soils is reviewed. Because of many emission sources, As is ubiquitous. Thermodynamic calculations revealed that As(V) species (HAsO 4 2- >H2AsO 4 - at pH 7) are more abundant in soil solutions that are oxidized more than pe+pH>9. Arsenic is expected to be in As(III) form (HAsO 2 0 =H3AsO 3 0 >AsO 2 - =H2AsO 3 - at pH 7) in relatively anoxic soil solutions with pe+pH<7. Adsorption on soil colloids is an important As scavenging mechanism. The adsorption capacity and behavior of these colloids (clay, oxides or hydroxides surfaces of Al, Fe and Mn, calcium carbonates, and/or organic matter) are dependent on ever-changing factors, such as hydration, soil pH, specific adsorption, changes in cation coordination, isomorphous replacement, crystallinity, etc. Because of the altering tendencies of soil colloids properties, adsorption of As has become a complex, empirical, ambiguous, and often a self contradicting process in soils. In general, Fe oxides/hydroxides are the most commonly involved in the adsorption of As in both acidic and alkaline soils. The surfaces of Al oxides/hydroxides and clay may play a role in As adsorption, but only in acidic soils. The carbonate minerals are expected to adsorb As in calcareous soils. The role of Mn oxides and biogenic particles in the As adsorption in soils appears to be limited to acidic soils. Kinetically, As adsorption may reach over 90% completion in terms of hours. Precipitation of a solid phase is another mechanism of As removal from soil solutions. Thermodynamic calculations showed that in the acidic oxic and suboxic soils, Fe-arsenate (Fe3(AsO4)4)2) may control As solubility, whereas in the anoxic soils, sulfides of As(III) may control the concentrations of the dissolved As in soil solutions. In alkaline acidic oxic and suboxic soils, precipitation of both Fe- and Ca-arsenate may limit As concentrations in soil solutions. Field observations suggest that direct precipitation of discrete As solid phases may not occur, except in contaminated soils. Chemisorption of As oxyanions on soil colloid surfaces, especially those of Fe oxide/hydroxides and carbonates, is believed to a common mechanisms for As solid phase formation in soils. It is suggested that As oxyanions gradually concentrate on colloid surfaces to a level high enough to precipitate a discrete or mixed As solid phase. Arsenic volatilization is another As scavenging mechanism operating in soils. Many soil organisms are capable of converting arsenate and arsenite to several reduced forms, largely methylated arsines which are volatile. These organisms may generate different or similar biochemical products. Methylation and volatilization of As can be affected by several biotic (such as type of organisms, ability of organism for methylation, etc.) and abiotic factors (soil pH, temperature, redox conditions, methyl donor, presence of other ions, etc.) factors. Information on the rate of As biotransformations in soils is limited. In comparison to the biologically assisted volatilization, the chemical volatilization of As in soils is negligible.  相似文献   

11.
Phosphorus (P) dynamics and availability in soils are influenced by P fertilization. This paper aimed to evaluate inorganic P fractions bonded to calcium (Ca), iron (Fe), and aluminum (Al), associating them with soil mineralogy. The experiment was carried out using an acidic kaolinitic–oxidic soil, located in an irrigated area cultivated with coffee plants (Coffee arabica L.), submitted to successive annual fertilizations with triple superphosphate doses of 0, 50, 100 200, and 400 kg ha?1 phosphorus pentoxide (P2O5) in randomized blocks with three replications. Phosphorus fractions were determined in soil samples collected at two depths, 0–10 and 10–20 cm, according to the methodology used by Chang and Jackson (1957 Chang, S. C. and Jackson, M. L. 1957. Fractionation of soil phosphorus. Soil Science, 84: 133–144. [Crossref] , [Google Scholar]). The inorganic P fractions presented the following sequence: P-Al > P-Fe > P-Ca. The dynamics of forms of inorganic P showed that P-Al is controlling the P bioavailability as a result of an acidic pH and a very simple and thermodynamically stable clay mineralogy, typical of very weathered and old tropical soils.  相似文献   

12.
Radiotracer experiments on the sorption of I? (iodide) and IO inf 3 p? (iodate) from water by soils such as field soil, rice paddy soil and sandy soil, as well as by some soil components, have been carried out with special reference to the effects of heating and gamma-irradiating the soil. Desorption phenomena of I from soil to various solutions were also studied. The sorption of I? by soil was markedly reduced through treatments of air-drying and heating the soil prior to its equilibration with water. The results indicated that I? sorption was by the soil fraction which was unstable at about 150 °C, while IO inf 3 p? sorption was by the soil fraction which was relatively stable to heating. Gamma-irradiation at 27 kGy affected the sorption to a smaller extent than heating at 150 °C. A very high sorption (or soil-water distribution coefficient, Kd) was found in untreated field soil (andosol) with a low organic C (humus) content, while the sorption by sandy soil was considerably smaller than the other soils. Neither I? or IO inf 3 p? were well sorbed by clay minerals, Al2O3 and quartz sand, while the sorption by Fe2O3 was IO inf 3 p? were desorbed by 1N NaOH solution. By acidifying this solution, only a part of the desorbed I was re-precipitated with humic acid. The desorption by solutions containing K2SO3 or KI was also high, while that by solutions containing HCI, CH3COONH4 or chemical fertilizer was considerably lower. These findings suggested the possibility that I was not directly associated with humic acid itself.  相似文献   

13.
Abstract

Critical limit (CL) determination of zinc (Zn) is very important for predicting response of maize crop to its application in soils and for the crop’s actual fertilizer requirement. This study was conducted at Bangladesh Agricultural Research Institute, Gazipur, to determine the CL of Zn for maize grown in 20 soils collected from the five Agro–Ecological Zones during January to March, and April to June of 2017. The available Zn content of soils and maize biomass were estimated utilizing the extraction method with 0.005?M diethylene triamine pentaacetic acid (DTPA). During January to March and April to June 2017, the amount of DTPA extractable Zn in different soils ranged from 0.60–3.25?mg?kg?1 and 0.50–1.68?mg?kg?1, respectively. During both periods of crop growth (January to March and April to June, 2017), the soil available zinc was negatively significantly correlated with soil pH, available P, exchangeable Ca, exchangeable Mg and positively significantly correlated with relative dry matter (DM) yield. Soil Zn also positively significantly correlated with maize tissue Zn content (r?=?0.521*). However, the CL of Zn were estimated to be 0.84?mg kg?1 in soils and 26.1?mg kg?1 in maize tissue for maize cropping as determined by Cate and Nelson’s (1965 Cate, R. B., and L. A. Nelson. 1965. A rapid method for correlation of soil test analysis with plant response data. International soil testing series technical Bulletin No. I North Caroline State University, Agricultural Experiment Statistics, Releigh, USA, pp. 135–136. [Google Scholar]) graphical procedure. Maize crop may respond to Zn application in soils containing Zn at/below the above level. This data may be used for predicting plant response to Zn fertilizer and development of crop Zn nutrition guide for maximum production.  相似文献   

14.
In the absence of SO infin4 sup= and NO inf3 su? in precipitation, the pH of precipitation is primarily a function of CO2?20 equilibria. Soil CO2 and organic acids, acquired during descent through soil profiles, augment the dissolving capacity of the solutions which initially may have a pH of 4 or lower. The recent man-related increase of H2SO4 and HNO3 in rainfall results in a significant lowering of pH in incident precipitation and an increase in corrosiveness of soil solutions. H2SO4 and HNO3 may contribute some Eh buffering capacity. Particularly susceptible to these changes are clay minerals and redox sensitive elements such as Fe, Mn, Ni, and Co. The overall chemical weathering trends associated with increased acidity of rainfall will be de-stabilization and eventual solution of clay minerals (and the loss of their cation exchange capacity), increased rates of chemical denudation, and solution of illuvial Fe and Al oxides and hydroxides. The latter results in the loss of the adsorbed and coprecipitated metal trace elements associated with these highly reactive phases. The general result in soils developed on non-carbonate substrates is a tendency toward extensive podsolization, with associated decrease in clay minerals, loss of cation exchange capacity, and decrease in fertility.  相似文献   

15.
On the productivity of paddy field, many investigations have been performed in Japan. These investigations were mainly focused on the importance of mineralization of soil organic nitrogen, redox system, and generation of injurious materials under water-logged conditions of soils. Recently HARADA (1) and YOSHIDA (2) showed that the cations adsorbed by negative charges originated from humic substances were more weaker than that of the clay. Moreover KONISHI (3) has investigated on the effects of Renge application upon the soil productivity and the leaching of nutrients. He proved that the applicatign of Renge upon soil accelerates the nutrient leaching. From these experiments the importance of nutrient leaching in the soil productivity was again closed up.  相似文献   

16.
Nonexchangeable potassium (K-ne), i.e. 1 M NH4OAc-nonexchangeable K, often contributes significantly to plant nutrition. However conventional extraction methods often extract much more K-ne than plants even after intensive cropping, suggesting the difficulty in evaluating the amount of readily available soil K-ne. In this study, we used a milder extraction method (0.01 M HCl method) to examine its applicability to evaluate the amount of readily available K-ne in soil. In the first experiment, the concentration of K-ne in twenty surface soils sampled from agricultural fields in Japan and K-bearing minerals was determined by the 0.01 M HCl method, i.e. sequential extraction with 0.01 M HCl over a period of 10 d after removal of exchangeable K, and by conventional methods. The average percentage of the soil K-ne extracted by the 0.01 M HCl method amounted to 0.66% of the total K amount, and was much lower than that by a single extraction with 1 M HNO3 (2.0%) or with 0.2 M sodium tetraphenylboron for 2 d (22%). In the second experiment, the amount of K-ne removed by chemical extractions was compared with that of K-ne removed by maize plants grown for 29 d in five of the above soils. The amount of the K-ne evaluated by the 0.01 M HCl method gave the highest correlation (p < 0.05) with that of the K-ne utilized by plants among the extraction methods applied. The amount of soil K-ne extracted by the 0.01 M Hel method could therefore become a suitable index of the amount of readily available K-ne in soil. Extraction of K-ne in soils after maize planting further indicated that plants had removed K-ne more intensively than the 0.01 < HCl method probably only from the rhizosphere, although a high correlation was observed between the amount of K-ne removed by the 0.01 M Hel method and that by plants. This implies that the estimation of the amount of K-ne utilized by plants requires not only soil chemical analysis but also the evaluation of the percentage of the soil volume where the plant-induced release of K-ne actually occurs.  相似文献   

17.
A pot culture experiment was conducted to investigate the effect of increasing levels (30.0 and 60.0 mg kg?1 soil) of chromium and lead on the yield, chemical composition of essential oil, and phytoaccumulation of heavy metals of three mint species (Mentha arvensis, M. piperita, and M. citrata). The fresh herbage yield of M. arvensis was not significantly affected by the application of chromium and lead, but its essential oil yield was significantly decreased by the application of chromium and lead as compared to the control. The fresh herbage, root yield, and essential oil yield of M. piperita were significantly increased and those of M. citrata were decreased by the increase in the levels of chromium and lead applications. The levels of α-pinene, β-pinene, sabinene, β-myrcene, limonene, menthone, and isomenthone in M. arvensis and M. piperita oil and of sabinene, pinene, and linalyl acetate in M. citrata oil were considerably affected by the application of chromium and lead to soils as compared to control plants. The concentrations of chromium in shoots and roots of mint species significantly increased as the levels of chromium in soil increased. The increases in the levels of lead in soil enhanced the concentrations of lead in the shoots and roots of mint species as compared to the control. The accumulations of chromium and lead were greater in the roots than in the shoots in all the three species of mint. Mentha piperita was found to be the most suitable crop for cultivation in the chromium- and lead-contaminated soils, followed by M. arvensis and M. citrata.  相似文献   

18.
The effects of elevated atmospheric SO 4 2? deposition on S cycling in forest soils were assessed in an irrigation experiment using stable S isotopes. Over a period of 20 months, core lysimeters of five acidic forest soils from Southern Germany with different parent material and pedogenesis were irrigated with solutions chemically similar to canopy throughfall. Sulfate deposition in three experimental variants corresponded to 23, 42 and 87 kg S ha?1 yr?1. The SO 4 2? used for irrigation had aδ 34S ratio of +28.0‰ CDT (Canon Diablo Troilite standard), differing by more than +25‰ from natural and anthropogenic S in Southern Germany. A combination of chemical and isotopic analyses of soil and seepage water samples was used to elucidate the fluxes and transformations of simulated wet SO 4 2? deposition in each soil core. Retention of experimentally deposited S ranged from 57±5% in coarse-grained soils low in sesquioxides and clay, to 80±8% in loamy soils with high sesquioxide content. The sesquioxide content proved to be the major factor governing S retention. The ratio of S retained as inorganic SO 4 2? (mainly by adsorption) to that incorporated into organic compounds (presumably by microbial synthesis) ranged from 2 to 4. For the organic S pool, the amount of S retained as C-bonded S exceeded by far that immobilized as ester sulfate in four of the five soils. Application of34S-enriched SO 4 2? appears to be a suitable experimental tool to assess fluxes and transformations of deposited S in forest soils, if aerobic conditions are maintained. In contrast to radioactive S tracers, the concept should be applicable not only in laboratory and lysimeter experiments, but also in long term studies of whole forest ecosystems (e.g., experimental watersheds).  相似文献   

19.
Fundamental knowledge about decomposition, fate of crop residue, and allocation of residue-derived carbon (C) in soil aggregates is essential to understand the C dynamics in soil. The incorporation of C derived from corn residue in water-stable aggregate fractions, particulate organic C (POC), and mineral-associated C (MAC) in soil were examined using the 13C tracer technique. Soil was treated with corn straw at the rate of 1% dry mass of soil brought to 66% of field capacity and incubated for 70 days at 25 °C. Samples were taken at 20, 35, and 70 days and analyzed for water-stable aggregates. Values for POC and MAC were analyzed for total C and 13C enrichment. The addition of corn straw caused a shift in the distribution of recoverable particles with significant decreases in <53-μm silts and clays, microaggregrates (53–250 μm), and smaller macroaggegates (250–2000 μm); however, the large macroaggegates (>2000 μm) increased significantly. Macroaggregates contained greater amount of C than microaggregates. The proportion of 13C recovered in the fractions <53 μm (silt and clay), 53–250 μm, and 250–2000 μm increased during decomposition of corn straw, whereas there was no significant change in >2000-μm fraction. Most (70–76%) of the soil organic C was affiliated with MAC (<53 μm). Carbon (13C) derived from corn straw decreased in POC but increased in MAC as decomposition proceeded. In the long term, microaggregate fraction appears to be involved in storage and stabilization of the C derived from corn straw and is important for soil quality and soil C sequestration point of view.  相似文献   

20.
  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号