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1.
Potassium (K) and nitrogen (N) are essential nutrients for plants. Adsorption and desorption in soils affect K+ and NH + 4 availabilities to plants and can be affected by the interaction between the electrical double layers on oppositely charged particles because the interaction can decrease the surface charge density of the particles by neutralization of positive and negative charges. We studied the effect of iron (Fe)/aluminum (Al) hydroxides on desorption of K+ and NH + 4 from soils and kaolinite and proposed desorption mechanisms based on the overlapping of diffuse layers between negatively charged soils and mineral particles and the positively charged Fe/Al hydroxide particles. Our results indicated that the overlapping of diffuse layers of electrical double layers between positively charged Fe/Al hydroxides, as amorphous Al(OH) 3 or Fe(OH) 3 , and negatively charged surfaces from an Ultisol, an Alfisol, and a kaolinite standard caused the effective negative surface charge density on the soils and kaolinite to become less negative. Thus the adsorption affinity of these negatively charged surfaces for K+ and NH + 4 declined as a result of the incorporation of the Fe/Al hydroxides. Consequently, the release of exchangeable K+ and NH +4 from the surfaces of the soils and kaolinite increased with the amount of the Fe/Al hydroxides added. The greater the positive charge on the surfaces of Fe/Al hydroxides, the stronger was the interactive effect between the hydroxides and soils or kaolinite, and thus the more release of K+ and NH + 4 . A decrease in pH led to increased positive surface charge on the Fe/Al hydroxides and enhanced interactive effects between the hydroxides and soils/kaolinite. As a result, more K+ and NH + 4 were desorbed from the soils and kaolinite. This study suggests that the interaction between oppositely charged particles of variable charge soils can enhance the mobility of K+ and NH + 4 in the soils and thus increase their leaching loss. 相似文献
2.
高岭石,蒙脱石和针铁矿对泥炭腐殖酸的吸附和分离 总被引：6，自引：0，他引：6
Sorption of humic acid (HA) on mineral surfaces has a profound interest regarding the fate of hydrophobic organic contaminants (HOCs) and carbon sequestration in soils. The objective of our study is to determine the fractionation behavior of HA upon sorption on mineral surfaces with varying surface properties. HA was coated sequentially on kaolinite (1:1 clay), montmorillonite (2:1 clay), and goethite (iron oxide) for four times. The unadsorbed HA fractions were characterized by elemental analysis, diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), and solid state 13C nuclear magnetic resonance spectroscopy (NMR). The mineral-HA complexes were characterized by DRIFT. Polarity index [(N+O)/C] revealed higher polarity of the unadsorbed HA fractions after coating on kaolinite, reflecting that relatively higher polarity fractions of HA remain unadsorbed. Sorption of aliphatic alcohol fraction along with carbohydrate was prominent on kaolinite surface. DRIFT results of the unadsorbed HA fractions indicated more sorption of aliphatic moieties on both kaolinite and montmorillonite. DRIFT results of the unadsorbed HA fractions after sorption on kaolinite and goethite showed the sorption of the proteinaceous fractions of HA. The HA fractions obtained after coating on goethite showed significant sorption of carboxylic moieties. The results mentioned above comply reasonably well with the DRIFT spectra of the mineral-HA complexes. 13C NMR results showed higher sorption of anomeric C on kaolinite surface. Higher sorption of paraffinic fraction was observed on montmorillonite. NMR data inferred the sorption of carboxylic moieties on goethite surface. Overall, this study showed that aliphatic moieties of HA preferentially sorbed on kaolinite and montmorillonite, while carboxylic functional groups play a significant role in sorption of HA on goethite. The sorbed fractions of HA may modify the mineral surface properties, and thus, the interaction with organic contaminants. 相似文献
3.
Chemical characteristics of humic substances in soils with different mineralogical characteristics and under different utilization paterns in Zhangpu,Fujian Province,together with two pairs of cultivated soils in North China Plain were studied by chemical analysis,visible and IR spectroscopy and ^13C NMR spectrometry.For soils in Zhanpu the HA/FA ratio and both the aromaticity and the degree of humification of HA were higher in soils with montmorillonite as the predominant clay mineral than in those with kaolinite as the predominant clay mineral,provided these soils were under the same utilization pattern.While for each pair of soils with similar mineralogical characteristics the HA/FA ratio was higher and the C/H ratio and the contnet of carboxyl group of HA were lower in paddy soil than in upland soil.Among the upland soils(or paddy soils)studied the Ha/FA ratio of soil in Zhangpu with kaolinite as the predominant clay mineral was the lowest,and that of soil in Zhangpu with montmorillonite as the predominant clay mineral was the highest .the lowest.and that of soil in Zhangpu with montmorillonite as the predominant clay mineral was the highest It was concluded that the presence of montmorillonite favored the fromation and maturation of humic acid. 相似文献
4.
Equilibrium and kinetic studies have been made on the adsorption of acrylonitrile(CH2=CHCN) on three soils and four minerals from aqueous solutions.It was shown that the organic matter was the major factor affecting the adsorption process in the soils.The conformity of the equilibrium data to linear type(one soil) and Langmuir type(two soils) isotherms indicated that different mechanisms were involved in the adsorption.This behavior appears bo be related to the hydrophobicity of soil organic matter due to their composition and E4/E6 ratio of humic acids.The adsorption kinetics were also different among the soils,indicating the difference in porosity of organic matter among the soils,and the kinetics strongly affected the adsorption capacity of soils for acrylonitrile.Acrylonitrile was slightly adsorbed from aqueous solutions on pyrophyllite with electrically neutral and hydrophobic nature,and practically not on montmorillonite and kaolinite saturated with Ca.However,much higher adsorption occurred on the zeolitized coal ash,probably caused by high organic carbon content(107g/kg). 相似文献
5.
湿地土壤NH4+吸附解吸对冻融循环的响应 总被引：3，自引：0，他引：3
YU Xiao-Fei ZHANG Yu-Xi ZOU Yuan-Chun ZHAO Hong-Mei LU Xian-Guo WANG Guo-Ping 《土壤圈》2011,21(2):251-258
Nitrogen (N) cycling in boreal peatland ecosystems may be influenced in important ways by freeze-thaw cycles (FTCs).Adsorption and desorption of ammonium ions (NH + 4) were examined in a controlled laboratory experiment for soils sampled from palustrine wetland,riverine wetland,and farmland reclaimed from natural wetland in response to the number of FTCs.The results indicate that freeze-thaw significantly increased the adsorption capacity of NH + 4 and reduced the desorption potential of NH + 4 in the wetland soils.There were significant differences in the NH + 4 adsorption amount between the soils with and without freeze-thaw treatment.The adsorption amount of NH + 4 increased with increasing FTCs.The palustrine wetland soil had a greater adsorption capacity and a weaker desorption potential of NH + 4 than the riverine wetland soil because of the significantly higher clay content and cation exchange capacity (CEC) of the riverine wetland soil.Because of the altered soil physical and chemical properties and hydroperiods,the adsorption capacity of NH + 4 was smaller in the farmland soil than in the wetland soils,while the desorption potential of the farmland soil was higher than that of the wetland soils.Thus,wetland reclamation would decrease adsorption capacity and increase desorption potential of NH + 4,which could result in N loss from the farmland soil.FTCs might mitigate N loss from soils and reduce the risk of water pollution in downstream ecosystems. 相似文献
6.
Xinhong GAN Ying TENG Jian XU Ning ZHANG Wenjie REN Ling ZHAO Peter CHRISTIE Yongming LUO 《土壤圈》2022,(2)
Clay minerals play an important role in biogeochemical cycling.Here,kaolinite and montmorillonite,the two most abundant and widespread clay minerals with typical layered structures,were selected to investigate and compare their effects on the biodegradation of benzo[a]pyrene(BaP)by Paracoccus aminovorans HPD-2 and to investigate the underlying interface mechanisms.Overall,the BaP degradation efficiency was significantly higher 7 d after montmorillonite addition,reaching 68.9%(P<0.05),when compared with that of the control without addition of clay minerals(CK,61.4%);however,the addition of kaolinite significantly reduced the BaP degradation efficiency to 45.8%.This suggests that kaolinite inhibits BaP degradation by inhibiting the growth of strain HPD-2,or its strong hydrophobicity and readily agglomerates in the degradation system,resulting in a decrease in the bio-accessibility of BaP to strain HPD-2.Montmorillonite may buffer some unfavorable factors,and cells may be fixed on the surface of montmorillonite colloidal particles across energy barriers.Furthermore,the adsorption of BaP on montmorillonite may be weakened after swelling,reducing the effect on the bio-accessibility of BaP,thus promoting the biodegradation of BaP by strain HPD-2.The experimental results indicate that differential bacterial growth,BaP bio-accessibility,interface interaction,and the buffering effect may explain the differential effects of the different minerals on polycyclic aromatic hydrocarbon biodegradation.These observations improve our understanding of the mechanisms by which clay minerals,organic pollutants,and degrading bacteria interact during the biodegradation process and provide a theoretical basis for increasing the biodegradation of soil pollutants by native microorganisms under field conditions. 相似文献
7.
有机酸对高岭石, 针铁矿和水铝英石吸附镉的影响 总被引：12，自引：0，他引：12
Effects of organic acids （oxalic, acetic, and citric） on adsorption characteristics of Cadmium （Cd） on soil clay minerals （kaolinite, goethite, and bayerite） were studied under different concentrations and different pH values. Although the types of organic acids and minerals were different, the effects of the organic acids on the adsorption of Cd on the minerals were similar, i.e., the amount of adsorbed Cd with an initial solution pH of 5.0 and initial Cd concentration of 35 mg L^-1 increased with increasing concentration of the organic acid in solution at lower concentrations, and decreased at higher concentrations. The percentage of Cd adsorbed on the minerals in the presence of the organic acids increased considerably with increasing pH of the solution. Meanwhile, different Cd adsorption in the presence of the organic acids, due to different properties on both organic acids and clay minerals, on kaolinite, goethite, or bayerite for different pHs or organic acid concentrations was found. 相似文献
8.
The particle-size distribution and mineralogical composition of the clay (< 2 μm) and fine-sand (0.25--0.10 mm) fractions in soils of two inland valleys in Abakaliki and Bende, Southeast Nigeria, were investigated to provide basic information on soil-forming processes and agricultural potentials. These soils were silty or clayey, deriving from Cretaceous or Tertiary shale materials. The particle-size distribution and its computation on a clay-free basis revealed relatively remarkable lithologic breaks in a couple of pedons. The effect of lithologic discontinuities on soil mineralogical composition was not, however, conspicuous. Petrographic investigation revealed that quartz predominantly comprised the fine-sand fraction in the soils at both study sites. Nevertheless, the clay mineralogical composition of the soils was a mixture of kaolinite, irregularly interstratified smectite-illite intergrades (S/I), hydroxyl-Al interlayered 2:1 type clays (HICs), vermiculite, smectite, halloysite and illite along with fine-sized quartz in Abakaliki. The soils of Bende predominantly contained smectite, which was partially interlayered with hydroxyl-Al and kaolinite. It is suggested that seasonal floodwater has slowed the disintegration of weatherable clay minerals inherited from the shale, while quartz originating from the sandstone is predominant in the fine-sand fraction. Additionally, a possible soil-forming process observed at the both study sites was ferrolysis, which was indicated by a clear decreasing pattern of HICs downward in the soil profiles. The entry of S/I and vertical distribution patterns for a couple of clay minerals in the pedon suggested that the soils in Abakaliki have developed under the significant influence of aeolian dust delivered by the harmattan. The findings might describe a site-specific deposition pattern of harmattan dusts as well as hydromorphic soil-forming processes in the wetlands of the inland valleys. 相似文献
9.
LI De-Cheng B. VELDE LI Feng-Min ZHANG Gan-Lin ZHAO Ming-Song HUANG Lai-Ming 《土壤圈》2011,21(4):522-531
Alfalfa cropping has been considered an efficient method of increasing soil fertility.Usually nitrogen increase in root nodules is considered to be the major beneficial effect.A 21-year time series (five sampling periods) of alfalfa cultivation plots on a loess soil,initially containing illite and chlorite,in Lanzhou of northwestern China was selected to investigate the relationships among alfalfa cropping,soil potassium (K) content and soil clay minerals.The results indicated that soil K significantly accumulated after cropping,with a peak value at about 15 years,and decreased afterwards.The accumulated K was associated with the K increase in the well-crystallized illite,which was not extracted by the traditional laboratory K extraction methods in assessing bioavailability.The steep decline in soil K content after 15-year cropping was in accord with the observed fertility loss in the alfalfa soil.Plant biomass productivity peaked at near 9 years of culture,whereas soil K and clay minerals continued to increase until cropping for 15 years.This suggested that K increased in the topsoil came from the deep root zone.Thus alfalfa continued to store K in clays even after peak production occurred.Nitrogen did not follow these trends,showing a general decline compared with the native prairie soils that had not been cropped.Therefore,the traditional alfalfa cropping can increase K content in the topsoil. 相似文献
10.
The characteristics of the reflectance spectra of clay minerals and their influences on the reflectance spectra of soils are dealt with in the paper.The results showed that dominant clay minerals in soils could be distinguished in light of the spectral -form parameters of the reflectance spectra of soils,thus making it possible to develop a quick method to determine clay minerals by means of reflectance spectra of soils in the lab.and providing a theoretic basis for remote sensing of clay minerals in soils with a high resolution imaging spectrometer. 相似文献
11.
《Communications in Soil Science and Plant Analysis》2012,43(11-12):1115-1126
Abstract Fixation of the ammonium ion (NH4 +) by clay minerals is an alternate way of building the nitrogen (N) pool in soil to optimize N crop recovery and minimize losses. Clay minerals (illite, montmorillonite, and vermiculite) and an illitic Portnoeuf soil were used to compare NH4 + fixation abilities. Total N determination and X‐ray diffraction analysis were performed on each of the minerals and the Portnoeuf soil controls, and NH4 + saturated batches were subsequently desorbed by potassium chloride (KCl) after 4096 hours. Total N was determined for each employing either Kjeldahl digestion only, or pretreating with hydrofluoric‐hydrochloric acid (HF‐HCl) before the Kjeldahl digestion. The total N for the soil was 38% more after pretreatment with HF‐HCl. The total N determined after pretreatment with HF‐HCl for the NH4 + saturated and subsequently KCl desorbed minerals was found to be highest in vermiculite. The cation exchange acapacity (CEC) of each of the minerals was determined, and highest CEC was found in montmorillonite [83.07 cmol(+)/kg]. X‐ray diffraction analysis revealed collapse of the vermiculitic clay lattice from an initial d‐spacing of 13.1 angstrom to 10.4 angstrom after desorprion by KCl. This suggested the existence of sequestered NH4 + between the 2: 1 vermiculitic clay interlayer lattice. 相似文献
12.
The kinetic (Km, Vmax) of alkaline phosphatase (AP) desorbed from different Ca-homoionic clay minerals (montmorillonite, illite, and kaolinite) by extraction with Tris-Malate-Citrate buffer solution (pH 9.6) was studied in model experiments. After extraction (shaking for 15 min.) the Km and Vmax were measured in the extract, the remaining sediment and in the whole set-up. With kaolinite and illite, Vmax of the desorbed AP was lower than that of the sediment. However, with montmorillonite, Vmax of AP in the extract and whole system increased if compared to the control, but decreased in the sediment. The Km of desorbed AP increased from 4.3 × 10?3 (control) to 5.0 × 10?3 M (illite), 5.4 × 10?3M (kaolinite), and 5.5 × 10?3M (montmorillonite). These values were lower than those obtained with the various sediments and whole experimental systems. An aberrant behaviour was recorded with the illite sorbed AP which showed an increase in affinity towards the substrate. Generally speaking, AP desorbed from clays may be reduced in its affinity towards the substrate p-nitrophenylphosphate by residual inhibitor and/or conformational change of the enzyme. 相似文献
13.
Fate of fertilizer ammonium in soils with different composition of clay minerals in an incubation experiment In an incubation experiment with three different soils (gray brown podsolic soil from loess, alluvial gley, and brown earth, derived from basalt) the specific adsorption (fixation) and release of fertilizer NH4+ was investigated. In one treatment 120 mg NH4–N/kg soil was added, while the other treatment (control) received no nitrogen. Soils samples were taken every ten days and analyzed for nonexchangeable and exchangeable NH4+ and NO3?. The experimental results are showing that the specific adsorption of applied NH4+ was related to the type of clay minerals. While the loess soil, rich in illite, and the alluvial soil, rich in expansible clay minerals, bound about 40% of the added NH4+ specifically, the soil derived from basalt with mainly kaolinite bound only about 10 %. From the recently “fixed” fertilizer NH4+ about a half was nitrified during the incubation period of about 9 weeks. In the control there was no significant release of specifically bound NH4+. Obviously this NH4+ is located more deeply in the interlayers of the clay minerals and not available to microorganisms. 相似文献
14.
水溶性有机碳在各种粘土底土中的吸附：土壤性质的影响 总被引：3，自引：0，他引：3
Clay-rich subsoils are added to sandy soils to improve crop yield and increase organic carbon (C) sequestration; however, little is known about the influence of clay subsoil properties on organic C sorption and desorption. Batch sorption experiments were conducted with nine clay subsoils with a range of properties. The clay subsoils were shaken for 16 h at 4 oC with water-extractable organic C (WEOC, 1 224 g C L-1) from mature wheat residue at a soil to extract ratio of 1:10. After removal of the supernatant, the residual pellet was shaken with deionised water to determine organic C desorption. The WEOC sorption was positively correlated with smectite and illite contents, cation exchange capacity (CEC) and total organic C, but negatively correlated with kaolinite content. Desorption of WEOC expressed as a percentage of WEOC sorbed was negatively correlated with smectite and illite contents, CEC, total and exchangeable calcium (Ca) concentrations and clay content, but positively correlated with kaolinite content. The relative importance of these properties varied among soil types. The soils with a high WEOC sorption capacity had medium CEC and their dominant clay minerals were smectite and illite. In contrast, kaolinite was the dominant clay mineral in the soils with a low WEOC sorption capacity and low-to-medium CEC. However, most soils had properties which could increase WEOC sorption as well as those that could decrease WEOC sorption. The relative importance of properties increasing or decreasing WEOC sorption varied with soils. The soils with high desorption had a low total Ca concentration, low-to-medium CEC and low clay content, whereas the soils with low desorption were characterised by medium-to-high CEC and smectite and illite were the dominant clay minerals. We conclude that WEOC sorption and desorption depend not on a single property but rather a combination of several properties of the subsoils in this study. 相似文献
15.
In upper mineral horizons, CEC by compulsive and isotopic exchange methods, using Ba2+ as the saturating cation, gave higher values than the effective CEC at natural soil pH, and much higher values than CEC determined with m NH4OAc at pH 7. Cumulative Al release during leaching was considerably higher using Mg2+ and Ba2+ chlorides than K+ and NH4+ chlorides, and gave a different shape extraction curve. Basal spacing of the dominant dioctahedral vermiculite in the soil clays contracted from 14.5Å to 10.0–10.9 Å when saturated with NH4+ and K+, restricting release of interlayer Al. Lower horizons, containing a large proportion of Al-chlorite in the clay fraction, which did not contract with any of the cations, showed more normal exchange behaviour. On leaching, Al release was slightly greater with K+ and NH4+, than with Mg2+ and Ba2+, chlorides. The implication of the results for CEC measurements is discussed. 相似文献
16.
The fraction of nonexchangeable ammonium (NH4+) can play an important role in N cycling of soils as a sink (fixation) or a source (release) of NH4+. Recently fixed nonexchangeable NH4+ especially seems to be a significant source for N release. The aim of our study was to determine the effect of residence time on the kinetics of nonexchangeable NH4+ release from illite and vermiculite. Calcium-saturated illite and vermiculite, containing NH4+ that was “fixed” for one and 60 d, were extracted with a H-resin for 0.25 to 384 h. Both clay minerals “fixed” significantly more NH4+ in 60 d than in 1 d, but vermiculite “fixed” more NH4+ than illite. The kinetics of nonexchangeable NH4+ release from illite and vermiculite were well described by the Elovich equation and by a heterogeneous diffusion model. In vermiculite the percentage of nonexchangeable NH4+ release decreased from 84% to 78% when the time of fixation increased from 1 to 60 d. In illite time of residence has not influenced the complete release of newly fixed NH4+. 相似文献
17.
中国土壤胶体研究——ⅥⅡ.五种主要土壤的粘粒矿物组成 总被引：3，自引：0，他引：3
粘粒矿物对土壤特性和肥力的意义是众所周知的。土壤胶体的特性主要决定于粘粒矿物的类型及其数量。随着土壤科学研究的进展,粘粒矿物组成的分析工作,已由定性分析逐渐进入到定量分析。在粘粒矿物的鉴定中,X射线分析是一个很重要的手段,也有用来进行粘粒矿物的定量分析,但由于不同土壤中的矿物结晶程度差异很大,所以侧定的准确性较差。因此,在土壤粘粒矿物分析方面,X射线一般只能作为定性和半定量之用,其分析结果往往用“主导”“伴随”“较多~较少”等术语来表示。目前这种表示粘粒矿物组成的方法已不能满足研究工作的需要,何况不同学者的判读标准又很难一致。 相似文献
18.
《Communications in Soil Science and Plant Analysis》2012,43(19-20):2783-2792
Abstract The effect of sesquioxides on the mechanisms of chemical reactions that govern the transformation between exchangeable potassium (Kex) and non‐exchangeable K (Knex) was studied on acid tropical soils from Colombia: Caribia with predominantly 2∶1 clay minerals and High Terrace with predominantly 1∶1 clay minerals and sesquioxides. Illite and vermiculite are the main clay minerals in Caribia followed by kaolinite, gibbsite, and plagioclase, and kaolinite is the major clay mineral in High Terrace followed by hydroxyl‐Al interlayered vermiculite, quartz, and pyrophyllite. The soils have 1.8 and 0.5% of K2O, respectively. They were used either untreated or prepared by adding AlCl3 and NaOH, which produced aluminum hydroxide. The soils were percolated continuously with 10 mM NH4OAc at pH 7.0 and 10 mM CaCl2 at pH 5.8 for 120 h at 6 mL h?1 to examine the release of Kex and Knex. In the untreated soils, NH4 + and Ca2+ released the same amounts of Kex from Caribia, whereas NH4 + released about twice as much Kex as Ca2+ from High Terrace. This study proposes that the small ionic size of NH4 + (0.54 nm) enables it to enter more easily into the K sites at the broken edges of the kaolinite where Ca2+ (0.96 nm) cannot have access. As expected for a soil dominated by 2∶1 clay minerals, Ca2+ caused Knex to be released from Caribia with no release by NH4 +. No Knex was released by either ion from High Terrace. After treatment with aluminum hydroxide, K release from the exchangeable fraction was reduced in Caribia due to the blocking of the exchange sites but release of Knex was not affected. The treatment increased the amount of Kex released from the High Terrace soil and the release of Knex remained negligible although with Ca2+ the distinction between Kex and Knex was unclear. The increase in Kex was attributed to the initially acidic conditions produced by adding AlCl3 which may have dissolved interlayered aluminum hydroxide from the vermiculite present, thus exposing trapped K as exchangeable K. The subsequent precipitation of aluminum hydroxide when NaOH was added did not interfere with the release of this K, and so was probably formed mostly on the surface of the dominant kaolinite. Measurement of availability of K by standard methods using NH4 salts could result in overestimates in High Terrace and this may be a more general shortcoming of the methods in kaolinitic soils. 相似文献
19.
Timtong Darunsontaya Anchalee Suddhiprakarn Irb Kheoruenromne Nattaporn Prakongkep Robert J. Gilkes 《Geoderma》2012
Potassium (K) deficiency is widespread in crops on highly weathered upland soils under a tropical monsoonal climate. Critical assessment of the forms of K in soils and of the ability of soils to release K for plant uptake is important for the proper management of K in crop production. The relationships between different pools of K were investigated as a function of silt and clay mineralogy for 14 upland Oxisols and 26 upland Ultisols soils from Thailand. Most soils contained no K-minerals in the silt fraction. XRD showed that kaolinite is the dominant clay mineral with variously minor or moderate amounts of illite, hydroxy-Al interlayered vermiculite and smectite present in some soils. For some soils, both conventional and synchrotron XRD were unable to detect illite. Analytical TEM including EFTEM of individual clay crystals showed that clay in the apparently illite-free samples contained very small amounts of illite. Many kaolinite particles appear to contain K which may be present in illite interleaved with kaolinite crystals. A glasshouse K-depletion experiment was conducted to assess the K supply capacity and changes in chemical forms of K and K-minerals using exhaustive K depletion by Guinea grass (Panicum maximum). Potassium deficiency symptoms and mortality of plants occurred on light textured soils, whereas plants survived for six harvests for Oxisols with clay texture, relatively high CEC and higher NH4OAc-K (exchangeable K plus water-soluble K). There is a strong linear relationship of unit slope between NH4OAc-K and cumulative K uptake by plants indicating that NH4OAc-K is a major form of K available to plants. Thus K-bearing minerals contributed little K to plants over the time scale of the experiment and XRD patterns of whole soil samples, silt and clay from soils after cropping mostly showed no change from those for the initial soil. An exception was for a single surface soil clay where a minor amount of smectite was formed from illite by K release to plants. 相似文献
20.
G. V. Shashkova I. I. Tolpeshta M. L. Sizemskaya T. A. Sokolova 《Eurasian Soil Science》2009,42(12):1348-1356
Different types of cation exchange capacity (CEC) and related chemical properties were determined in the main genetic horizons
of meadow-chestnut soils in the mesodepressions at the Dzhanybek Research Station of the Institute of Forestry of the Russian
Academy of Sciences. In the A horizon, the CEC is mainly due to the organic matter from the clay and coarse fractions, which
provides 36% of the soil CEC, and to labile silicates and other clay minerals of the clay fraction. In the Bt horizon, the
CEC is mainly provided by the labile minerals of the clay fraction and organic matter of the clay and coarse fractions. The
standard soil CEC was found to be significantly higher than the sum of the exchangeable cations in the A horizon and slightly
lower than the sum of the exchangeable cations in the Bt and Bca2 horizons. This difference can be related to the fact that
the NH4+ ion, which is selectively adsorbed by clay minerals, is used as a displacing cation during the determination of the exchangeable
bases, while the Ba2+ ion, which is more selectively adsorbed by organic matter, is used during the determination of the standard CEC. In all the
genetic horizons, the experimentally determined value of the standard CEC almost coincides with the CEC value obtained by
summing the standard CECs of the different particle-size fractions with account for their contents; hence, this parameter
is additive in nature. 相似文献