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1.
Soil acidity is the principal limiting factor in crop production in Oxisols, and deficiency of micronutrients has increased in recent years because of intensive cropping. A field experiment was conducted over three consecutive years to assess response of common bean (Phaseolus vulgaris L.) to lime and iron (Fe) applications on an Oxisol in a no-tillage system. Changes in selected soil chemical properties in the soil profile (0- to 10- and 10- to 20-cm depths) with liming were also determined. Lime rates used were 0, 12, and 24 Mg ha–1, and Fe application rates were 0, 50, 100, 150 200, and 400 kg ha–1. Both lime and Fe were applied as broadcast and incorporated in the soil. Grain yields of common bean were significantly increased with the application of lime. Iron application, however, did not influence bean yield. There were significant changes in soil profile (0- to 10-cm and 10- to 20-cm depths) in pH, calcium (Ca2+), magnesium (Mg2+), hydrogen + aluminum (H+ + Al3+), base saturation, acidity saturation, cation exchange capacity (CEC), Ca2+ saturation, Mg2+ saturation, potassium (K+) saturation, and ratios of Ca/Mg, Ca/K, and Mg/K. These soil chemical properties had significant positive association with common bean grain yield. Averaged across two depths and three crops, common bean produced maximum grain yield at pHw 6.3, Ca2+ 3.8 cmolc kg–1, Mg2+ 1.1 cmolc kg–1, 3.5 H+ + Al3+ cmolc kg–1, acidity saturation 41.8%, CEC 7.5 cmolc kg–1, base saturation 57.4%, Ca saturation 45.2%, Mg saturation 14.2%, K saturation 9.1%, Ca/Mg ratio 3.1, Ca/K ratio 22.6, and Mg/K ratio 6.7.  相似文献   

2.
This study was designed to evaluate changes in the dynamics of soil phosphorus and cationic balances of a savannah soil subjected to 45 years of continuous cultivation under different fertilizer management and later left fallow for 15 years. It was conducted on the experimental plots at the Institute for Agricultural Research, Ahmadu Bello University, Nigeria. Treatments consisted of nitrogen (N), phosphorus (P), potassium (K), cow dung manure (D) and their combination (DNPK). Results of P fractionation and cationic distribution were compared with previous studies on the same plot 15 years ago. Organic carbon increased from a range of 3–5 g kg?1 in 1997 to 10.9 g kg?1 in 2012. Similarly, the cation exchange capacity (CEC) of the soil increased from 6.40 cmolc kg?1 in 1997 to 16.4 cmolc kg1 in the present study. The degree of saturation of the CEC by Ca2+ was 68–79% and 10–20% for Mg2+, while that of K+ was 1.5–2%. Although there was an uneven trend in depletion and enrichment of the various P pools, however, the fallow period substantially improved the CEC and the plant available P pools of the soil by more than 200% and 6–259%, respectively.  相似文献   

3.
Charcoal‐based amendments have a potential use in controlling NH3 volatilization from urea fertilization, owing to a high cation‐exchange capacity (CEC) that enhances the retention of NH . An incubation study was conducted to evaluate the potential of oxidized charcoal (OCh) for controlling soil transformations of urea‐N, in comparison to urease inhibition by N‐(n‐butyl) thiophosphoric triamide (NBPT). Four soils, ranging widely in texture and CEC, were incubated aerobically for 0, 1, 3, 7, and 14 d after application of 15N‐labeled urea with or without OCh (150 g kg?1 fertilizer) or NBPT (0.5 g kg?1 fertilizer), and analyses were performed to determine residual urea and 15N recovery as volatilized NH3, mineral N (as exchangeable NH , NO , and NO ), and immobilized organic N. The OCh amendment reduced NH3 volatilization by up to 12% but had no effect on urea hydrolysis, NH and NO concentrations, NO accumulation, or immobilization. In contrast, the use of NBPT to inhibit urea hydrolysis was markedly effective for moderating the accumulation of NH , which reduced immobilization and also controlled NH3 toxicity to nitrifying microorganisms that otherwise caused the accumulation of NO instead of NO . Oxidized charcoal is not a viable alternative to NBPT for increasing the efficiency of urea fertilization.  相似文献   

4.
Recent studies have documented adverse affects of urea on the establishment and growth of aerobic rice when applied at seeding. The following experiments were conducted to examine the relative importance of ammonia and nitrite (NO$ _2^- $ ) toxicities as mechanisms contributing to poor germination and early growth of aerobic rice. Soil was collected from an experiment in the Philippines where aerobic rice was grown continuously for 7 years. Subsamples of the soil were: (1) pretreated with sulfuric acid (0.5 M H2SO4 added at 75 mL kg–1), (2) oven‐heated at 120°C for 12 h, or (3) left untreated. In a greenhouse study N was applied to the untreated, acidified, and oven‐heated soils as either urea or ammonium sulfate (0.0 or 0.3 g N kg–1). Plant height, root length, total biomass, and number of seminal roots were evaluated after 10 d. Microdiffusion incubations were used to assess the effects of soil pretreatment, N source, and N rate (0, 0.5, 1.0, 1.5 g N kg–1) on ammonia (NH3) volatilization and germination. Nitrite incubations were conducted to establish a critical level for NO$ _2^- $ toxicity and measure the extractable NO$ _2^- $ and germination trends as affected by soil pretreatment, N source, and N rate. On untreated soil, urea reduced early growth and germination while ammonium sulfate caused no adverse effects. Progressively higher rates of urea increased NH3 volatilization and inhibited germination, while oven‐heating and acidification minimized the adverse effects. All treatment combinations (soil pretreatment, N source, N rate) had extractable NO$ _2^- $ levels below the critical level of 0.2 g N kg–1, suggesting that ammonia and not NO$ _2^- $ toxicity was the principal cause of inhibition. Since the risk of NH3 toxicity is highest just following urea hydrolysis, strategies to optimize the timing and placement of urea should be considered.  相似文献   

5.
ABSTRACT

A field study was conducted with the objective of determining response of dry bean (Phaseolus vulgaris L.) to liming and copper (Cu) fertilization applied to an Oxisol. The lime rates used were 0, 12, and 24 Mg ha?1 and Cu rates were 0, 2.5, 5, 10, 20, and 40 kg Cu ha?1. Liming significantly increased common bean grain yield. Liming also significantly influenced soil chemical properties in the top (0–10 cm) as well as in the sub (10–20 cm) soil layer in favor of higher bean yield. Application of Cu did not influence yield of bean significantly. Average soil chemical properties across two soil layers (0–10 and 10–20 cm) for maximum bean yield were pH 6.4, calcium (Ca), 4.2 cmolc kg?1, magnesium (Mg) 1.0 cmolc kg?1, H+Al 3.2 cmolc kg?1, acidity saturation 40.4%, cation exchange capacity (CEC) 8.9 cmolc kg?1, base saturation 63.1%, Ca saturation 45.7%, Mg saturation 18.0%, and Potassium (K) saturation 2.9.  相似文献   

6.
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   

7.
Acid soils in some mediterranean forests were investigated for the composition of the adsorption complex and the gradients in soil pH. The effective CEC (235–838 mmolc kg?1) and base saturation (93–98 %) are highest in ectorganic horizons. In the mineral horizons the effective CEC (23–52 mmolc kg?1) and base saturation (11–40 %) are much lower. The exchange complex of mineral horizons consists for 90 (AEh) to 40 percent (Bw2) of organic matter. The effective CEC of the mineral clay fraction is low (60 mmolc kg?1 clay). The clear trends in soil pH within the ectorganic layer of deciduous and sclerophyllous oak forests are attributed to vertical spatial separation of nitrogen mineralization (ammonification and strongly impeded nitrification) and nutrient uptake by roots (mainly NH4). This leads to a high effective CEC in the fermentation layer and acidification of the uppermost part of the mineral soil. In contrast to the situation in temperate forests this process is impeded in mediterranean coniferous forests, where litter decomposition is extremely slow and both proton production and consumption take place in the organic rich mineral horizon.  相似文献   

8.
Potassium (K) exchange isotherms (quantity–intensity technique, Q/I) and K values derived from the Q/I relationship provide information about soil K availability. This investigation was conducted to study Q/I parameters of K, available K extracted by 1 N ammonium acetate (NH4AOc) (exchangeable K plus solution K), K saturation percentage (K index, %), and the properties of 10 different agricultural soils. In addition, the relationship of mustard plant yield response to the K requirement test based on K exchange isotherms was investigated. The Q/I parameters included readily exchangeable K (ΔK0), specific K sites (KX), linear potential buffering capacity (PBCK), and energy of exchange of K (EK). The results of x-ray diffraction analysis of the oriented clay fractions indicated that some mixed clay minerals, illite clay minerals, along with chlorite/hydroxy interlayered vermiculite and kaolinite were present in the soils. The soil solution K activity ratio at equilibrium (AR0) ranged from 8.0 × 10?4 to 3.1 × 10?3 (mol L?1)0.5. The readily exchangeable K (ΔK0) was between 0.105 to 0.325 cmolckg?1 soil, which represented an average of 88% of the exchangeable K (Kex). The soils showed high capacities to maintain the potential of K against depletion, as they represented high linear potential buffering capacities (PBCK) [13.8 to 50.1 cmolc kg?1/(mol L?1)0.5. The EK values for the soils ranged from ?3420 to ?4220 calories M?1. The percentage of K saturation (K index) ranged from 0.7% to 2.2%. Analysis of variance of the dry matter (DM), K concentrations, and K uptake of mustard plants indicated that there were no significant differences among the adjusted levels of K as determined by the exchange-isotherm curve.  相似文献   

9.
In Saxony‐Anhalt, Germany, an area of about 6000 ha is covered by lignite‐ash‐derived substrates. In some cases, pollutants like heavy metals or toxic organic compounds had been disposed of together with the lignite ashes. For this reason, we assessed factors influencing the cation exchange capacity (CEC) of lignite‐ash substrates exposed to natural weathering. We chose four research sites reflecting the different methods of disposal: two dumped landfills and two lagooned ashes of different ages. After determining the CEC at pH 8.1 (CECpot), we evaluated the influence of the content of silt and clay and the content of total organic C. As lignite‐ash‐derived substrates are rich in oxalate‐extractable Si, Al, and Fe, we performed an oxalate extraction and determined afterwards the CECpot to assess the contribution of oxalate‐soluble compounds to the CECpot. Moreover, we determined the variable charge of selected samples at pH values ranging from 4 to 7. The lignite‐ash‐derived soils had a high CECpot with means ranging from 25.1 cmolc kg–1 to 88.8 cmolc kg–1. The influence of the parent material was more important than the degree of weathering. The content of total organic C consisting of pedogenic organic matter and coked lignite particles together with the content of silt and clay played a statistically significant role in determining the CEC. Another property that influenced the amount of CEC in medium textured lignite ashes was the content of oxalate‐soluble silica and aluminum. After oxalate extraction, they lost about 30% of their CEC due to the dissolution of oxalate‐soluble compounds. In coarse textured lignite ashes, oxalate extraction led to higher amounts of CEC, probably due to an increase of surface area resulting either from the disintegration of particles or from etching caused by insufficient dissolution of magnetite and maghemite. Moreover, lignite‐ash‐derived substrates exhibit a high amount of pH‐dependent charge. The CEC decreased by 40% in a topsoil sample and by 51% in a subsoil sample as the pH declined from 7 to 4.  相似文献   

10.
胡敏酸对铵钾在粘土矿物上交互作用的影响   总被引：1，自引：0，他引：1  
Interaction of ammonium (NH+4) and potassium (K+) is typical in field soils. However, the effects of organic matter on interaction of NH+4 and K+have not been thoroughly investigated. In this study, we examined the changes in major physicochemical properties of three clay minerals (kaolinite, illite, and montmorillonite) after humic acid (HA) coating and evaluated the influences of these changes on the interaction of NH+4 and K+on clay minerals using batch experiments. After HA coating, the cation exchange capacity (CEC) and specific surface area (SSA) of montmorillonite decreased significantly, while little decrease in CEC and SSA occurred in illite and only a slight increase in CEC was found in kaolinite. Humic acid coating significantly increased cation adsorption and preference for NH+4, and this effect was more obvious on clay minerals with a lower CEC. Results of Fourier transform infrared spectrometry analysis showed that HA coating promoted the formation of H-bonds between the adsorbed NH+4 and the organo-mineral complexes. HA coating increased cation fixation capacity on montmorillonite and kaolinite, but the opposite occurred on illite. In addition, HA coating increased the competitiveness of NH+4 on fixation sites. These results showed that HA coating affected both the nature of clay mineral surfaces and the reactions of NH+4 and K+with clay minerals, which might influence the availability of nutrient cations to plants in field soils amended with organic matter.  相似文献   

11.
Abstract

In Oxisols, acidity is the principal limiting factor for crop production. In recent years, because of intensive cropping on these soils, deficiency of micronutrients is increasing. A field experiment was conducted on an Oxisol during three consecutive years to assess the response of common bean (Phaseolus vulgaris L.) under a no‐tillage system to varying rates of lime (0, 12, and 24 Mg ha?1) and boron (0, 2, 4, 8, 12, 16, and 24 kg ha?1) application. Both time and boron (B) were applied as broadcast and incorporated into the soil at the beginning of the study. Changes in selected soil chemical properties in the soil profile (0- to 10‐ and 10- to 20‐cm depths) with liming were also determined. During all three years, gain yields increased significantly with the application of lime. However, B application significantly increased common bean yield in only the first crop. Only lime application significantly affected the soil chemical properties [pH; calcium (Ca2+); magnesium (Mg2+); hydrogen (H+)+ aluminum (Al3+); base saturation; acidity saturation; cation exchange capacity (CEC); percent saturation of Ca2+, Mg2+, and potassium (K+); and ratios of exchangeable Ca/Mg, Ca/K, and Mg/K] at both soil depths (0–10 cm and 10–20 cm). A positive significant association was observed between grain yield and soil chemical properties. Averaged across two depths and three crops, common bean produced maximum grain yield at soil pHw of 6.7, exchangeable (cmolc kg?1) of Ca2+ 4.9, Mg2+ 2.2, H++Al3+ 2.6, acidity saturation of 27.6%, CEC of 4.1 cmolc kg?1, base saturation of 72%, Ca saturation of 53.2%, Mg saturation of 17.6%, K saturation of 2.7%, Ca/Mg ratio of 2.8, Ca/K ratio of 25.7, and Mg/K ratio of 8.6. Soil organic matter did not change significantly with addition of lime.  相似文献   

12.
This paper describes the conditions for dispersion and flocculation of clays, and the impact of this process on soils of contrasting textures cropped with rice. Clay seems to be translocated down the profiles and along a topographic sequence. The clays are mixed kaolinite–smectite. The cation exchange capacity of these clays exceeds 20 cmolc kg?1. Both the proportion of smectite and clay content increase with increasing depth and from the top to the lower part of the sequence. The pH ranges from 5 to 8. The aluminium oxide content is small. The soil solutions collected during the rainy season were analysed for Fe2+ and major cations. We calculated the sodium adsorption ratios (SAR) taking into account Fe2+ and compared them with the critical coagulation concentration (CCC) found in a previous study. The Fe2+ contributed to a decrease in the SAR of cropped soils. The comparison between SAR, total electrolyte concentrations and CCC values showed that the dispersible clays are likely (i) to disperse in the abandoned and non‐saline fields, (ii) to flocculate in the saline and uncropped soils as a result of the large salt content and in the cropped soils because of either large salt or Fe2+ content, and (iii) to disperse in the flood water and at the surfaces of abandoned fields under rain. No evidence for ferrolysis was found. The observed contrasting textures and clay mineralogy can be explained by clay translocation controlled by salinity and rice farming.  相似文献   

13.

Purpose

Crop straws and animal manure have the potential to ameliorate acidic soils, but their effectiveness and the mechanisms involved are not fully understood. The aim of this study was to evaluate the effectiveness of two crop (maize and soybean) straws, swine manure, and their application rates on acidity changes in acidic red soils (Ferralic Cambisol) differing in initial pH.

Materials and methods

Two red soils were collected after 21 years of the (1) no fertilization history (CK soil, pH 5.46) and (2) receiving annual chemical nitrogen (N) fertilization (N soil, pH 4.18). The soils were incubated for 105 days at 25 °C after amending the crop straws or manure at 0, 5, 10, 20, and 40 g kg?1 (w/w), and examined for changes in pH, exchangeable acidity, N mineralization, and speciation in 2 M KCl extract as ammonium (NH4+) and nitrate plus nitrite (NO3??+?NO2?).

Results and discussion

All three organic materials significantly decreased soil acidity (dominated by aluminum) as the application rate increased. Soybean straw was as effective (sometimes more effective) as swine manure in raising pH in both soils. Soybean straw and swine manure both significantly reduced exchangeable acidity at amendment rate as low as 10 g kg?1 in the highly acidic N soil, but swine manure was more effective in reducing the total acidity especially exchangeable aluminum (e.g., in the N soil from initial 5.79 to 0.50 cmol(+) kg?1 compared to 2.82 and 4.19 cmol(+) kg?1 by soybean straw and maize straw, respectively). Maize straw was less effective than soybean straw in affecting soil pH and the acidity. The exchangeable aluminum decreased at a rate of 4.48 cmol(+) kg?1 per pH unit increase for both straws compared to 6.25 cmol(+) kg?1 per pH unit from the manure. The NO3??+?NO2? concentration in soil increased significantly for swine manure amendment, but decreased markedly for straw treatments. The high C/N ratio in the straws led to N immobilization and pH increase.

Conclusions

While swine manure continues to be effective for ameliorating soil acidity, crop straw amendment has also shown a good potential to ameliorate the acidity of the red soil. Thus, after harvest, straws should preferably not be removed from the field, but mixed with the soil to decelerate acidification. The long-term effect of straw return on soil acidity management warrants further determination under field conditions.
  相似文献   

14.
The objective of this laboratory study with six loess soils (three Eutric CambisoIs and three Haplic Phaeozems) incubated under flooded conditions was to examine the effect of a wide range of NO doses under anaerobic conditions on soil redox potential and N2O emission or absorption. Due to the fact that loess soils are usually well‐drained and are expected to be absorbers during prevailing part of the season, the study aimed at determination of the conditions decisive for the transition from emission to absorption process. On the basis of the response to soil nitrate level, the two groups of soils were distinguished with high and low denitrification capacity. The soil denitrification activity showed Michaelis‐Menten kinetics with respect to soil nitrate content with KM in the range 50–100 mg NO ‐N kg–1. Percentage of nitrates converted to N2O increased linearly with nitrate concentration in the range from 25 to 100 mg NO ‐N kg–1 up to 43% and decreased linearly at higher concentrations reaching practically zero at concentrations about 600 mg NO ‐N kg–1. No denitrification was observed below 25 mg NO ‐N kg–1. Nitrous oxide absorption in soil occurred only at nitrate concentrations to 100 mg NO ‐N kg–1 and in this concentration range was proportional to the denitrification rate. Nitrous oxide was formed at redox potentials below +200 mV and started to disappear at negative Eh values.  相似文献   

15.
This study investigated general physicochemical properties of tea garden soils at the alluvial plain of Cong River in Tan Cuong commune, Vietnam. Four gardens were selected as study sites on three transect lines established perpendicularly to the river. Soil samples were collected from the surface (0–10 cm) and subsurface (20–30 cm). Soil texture classes varied from sandy loam to light clay, which was affected by different terrains along the transect lines as well as severe disturbance such as terracing and earth excavation. The levels of total C and total N were correlated with increasing garden age, suggesting the replenishment of soil organic matter pool by the addition of plant residue and manure. Meanwhile, the soils showed strongly acidic nature with the average pH(H2O) of 3.7 at the surface and 3.9 at the subsurface. The effective cation exchange capacity (ECEC) was low at 4.7 and 4.9 cmolc kg?1, respectively, and dominated by exchangeable Al3+. Soil acidification was exacerbated with increasing garden age. However, a relatively large saturation of exchangeable calcium (Ca2+), potassium (K+), and magnesium (Mg2+) on the ECEC was found in the surface soils. The levels of available P were high, occasionally exceeding 1000 and 500 mg kg?1 at the surface and subsurface, respectively. In spite of strongly acidic condition, ammonium (NH4-N) applied as fertilizer was converted to nitrate (NO3-N) to move down to deeper layers. The levels of the bases, P, and mineral N seem to be principally determined by management practices. Significant portion of these nutrients was likely to exist in water soluble forms without adsorption onto soils. It should be required to develop proper schemes and to educate the owners for adequate fertilizer managements.  相似文献   

16.
Phosphorus (P) adsorbed by iron (Fe) oxyhydroxides in soil can be released when the Fe(III) minerals are reductively dissolved after soil flooding. However, this release is limited in tropical soils with large Fe contents and previous studies have suggested that P sorbs or precipitates with newly formed Fe(II) minerals. This hypothesis is tested here by scavenging Fe2+ in flooded soils by increasing the cation exchange capacity (CEC) of soil through resin application (30 cmolc kg?1; Na‐form). Three soils from rice paddies with contrasting properties were incubated in aerobic and anaerobic conditions with or without resin and with or without addition of organic matter (OM) to stimulate redox reactions. Dissolved Fe was 0.1–1.1 mm in unamended anaerobic soils and decreased to less than 0.07 mm with resin addition. Anaerobic soils without resin and aerobic soils with or without resin had marginal available P concentrations (<2 mg P kg?1; anion‐exchange membrane P). In contrast, available P increased 3‐ to 14‐fold in anaerobic soils treated with resins, reaching 16 mg P kg?1 in combination with extra OM. Application of Ca‐forms of resin did not stimulate P availability and dissolved Ca concentrations were larger than in unamended soils. Resin addition can increase P availability, probably by a combination of reducing solution Fe2+ (thereby limiting the formation of Fe(II) minerals) and increasing the OM solubility and availability through reducing dissolved Ca2+. The soil CEC is a factor controlling the net P release in submerged soils.  相似文献   

17.
Dispersion is an important issue for clay leaching in soils. In paddy soils of the Red River Delta (RRD), flooding with fresh water and relatively high leaching rates can accelerate dispersion and the translocation of clay. For the clay fraction of the puddled horizon of a typical paddy soil of the RRD, the effect of various cations and anions as well as humic acid (HA) at different pH values on the surface charge (SC) were quantified and the dispersion properties were determined in test tubes and described by the C50 value. In the <2 µm fraction, dominated by illite, the proportion of 2:1 vs. 1:1 clay minerals is 5:1. The organic‐C content of the clay fraction is 2.2%. Surface charge was found to be highly pH‐dependent. At pH 8 values of –32 and at pH 1 of –8 mmolc kg–1 were obtained. Complete dispersion was observed at pH > 4, where SC is > –18 mmolc kg–1. The flocculation efficiency of Ca strongly depends on the pH. At pH 4, the C50 value is 0.33, 0.66 at pH 5, and 0.90 mmol L–1 at pH 6. At pH 6, close to realistic conditions of paddy soils, the effect of divalent cations on the SC and flocculation decreases in the order: Pb > Cu > Cd > FeII > Zn > Ca > MnII > Mg; FeII was found to have a slightly stronger effect on flocculation than Ca. An increase in concentrations of Ca, MnII, and Mg from 0 to 1 mmol L–1 resulted in a change in SC from –25 to approx. –15 mmolc kg–1. In comparison, the divalent heavy‐metal cations Pb, Cu, Cd, and Zn were found to neutralize the SC more effectively. At a Pb concentration of 1 mmol L–1, the SC is –2 mmolc kg–1. From pH 3 to 5, the dispersion of the clay fraction is facilitated rather by SO than by Cl–, which can be explained by the higher affinity of SO to the positively charged sites. With an increase of the amount of HA added, the SC continuously shifts to more negative values, and higher concentrations of cations are needed for flocculation. At pH 3, where flocculation is usually observed, the presence of HA at a concentration of 40 mg L–1 resulted in a dispersion of the clay fraction. While high anion concentrations and the presence of HA counteract flocculation by making the SC more negative, FeII and Ca (C50 at pH 6 = 0.8 and 0.9 mmol L–1, respectively) are the main factors for the flocculation of the clay fraction. For FeII and Ca, the most common cations in soil solution, the C50 values were found to be relatively close together at pH 4, 5, and 6, respectively. Depending on the specific mineralogical composition of the clay fraction, SC is a suitable measure for the determination of dispersion properties and for the development of methods to keep clay particles in the soil in the flocculated state.  相似文献   

18.
Recent studies indicate that aerobic rice can suffer injury from ammonia toxicity when urea is applied at seeding. Urea application rate and soil properties influence the accumulation of ammonia in the vicinity of recently sown seeds and hence influence the risk of ammonia toxicity. The objectives of this study were to (i) evaluate the effects of urea rate on ammonia volatilization and subsequent seed germination for a range of soils, (ii) establish a critical level for ammonia toxicity in germinating rice seeds and (iii) assess how variation in soil properties influences ammonia accumulation. Volatilized ammonia and seed germination were measured in two micro‐diffusion incubations using 15 soils to which urea was applied at five rates (0, 0.25, 0.5, 0.75 and 1.0 g N kg?1 soil). Progressively larger urea rates increased volatilization, decreased germination and indicated a critical level for ammonia toxicity of approximately 7 mg N kg?1. Stepwise regression of the first three principal components indicated that the initial pH and soil texture components influenced ammonia volatilization when no N was added. At the intermediate N rate all three components (initial pH, soil texture and pH buffering) affected ammonia volatilization. At the largest N rate, ammonia volatilization was driven by soil texture and pH buffering while the role of initial pH was insignificant. For soils with an initial pH > 6.0 the risk of excessive volatilization increased dramatically when clay content was <150 mg kg?1, cation exchange capacity (CEC) was <10 cmolc kg?1 and the buffer capacity (BC) was <2.5 cmolc kg?1 pH?1. These findings suggest that initial pH, CEC, soil texture and BC should all be used to assess the site‐specific risks of urea‐induced ammonia toxicity in aerobic rice.  相似文献   

19.
It is well known that calcium (Ca2+) plays an important role in binding organic matter to clay. However, most previous studies were conducted with either topsoil or pure aluminosilicates. Less is known about the effect of Ca2+ on binding of organic matter to clay-rich subsoils, which have lower organic-matter contents than topsoils, and their clays are more strongly weathered than pure aluminosilicates. Two experiments were conducted with a Vertisol subsoil (69% clay): a laboratory incubation and a batch sorption. The mineral substrate in the incubation experiment was pure sand alone or sand amended with 300 g clay kg?1. Powdered calcium sulfate (CaSO4) at rates of 0, 5, 10, and 15 g Ca kg?1 and mature wheat residue at a rate of 20 g kg?1 were added to this mineral substrate and the water content was adjusted to 70% of water-holding capacity. Carbon dioxide release was measured for 28 days. Cumulative respiration per g soil organic carbon (C) (SOC from clay and residues) was increased by clay addition. Increasing Ca2+ addition rate decreased cumulative respiration in the sand with clay but had no effect on respiration in the pure sand. Clay and Ca2+ addition had no significant effect on microbial biomass carbon (MBC) per g SOC but clay addition reduced the concentration of potassium sulfate (K2SO4)–extractable C per g SOC. For the batch sorption experiment, the subsoil was mixed with 0 to 15 g Ca kg?1 and water-extractable organic C (WEOC) derived from mature wheat straw was added at 0, 1485, 3267, and 5099 mg WEOC kg?1. Increasing Ca2+ addition rate increased sorption of WEOC, particularly at the greatest concentration of WEOC added, and decreased desorption. This study confirmed the importance of Ca2+ in binding organic matter to clay and suggests that Ca2+ addition to clay-rich subsoils could be used to increase their organic C sequestration.  相似文献   

20.
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   

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