REACTIONS OF AMMONIA WITH SOIL. I

Heats of adsorption and adsorption isotherms of ammonia gas were measured at 300 K (27 °C) on outgassed soil saturated with Na⁺, K⁺, NH₄⁺, Ca²⁺, or Mg²⁺ ions. The Ca and Mg soils adsorbed apparently one more NH₂ molecule per exchangeable ion than the Na and K soils, mostly in the relative pressure range o to 0.005, but not much more than the NH₄ soil. The initial heat of adsorption was c. 75 kJ mol^-1 on the Ca and Mg soils and c. 60 kJ mol^-1 on the other soils. The results suggest that most NH, is sorbed on these soils through reactions not involving exchangeable cations.     

Potassium→ammonium exchange of two benchmark soils from Botswana and its implication for nitrogen economy of the soils

Ion exchange preferences for NH₄⁺ and K⁺ by soil exchanger surface can greatly affect the NO₃^? leaching into groundwater and nitrogen-use efficiency in agricultural production. Since NH₄⁺ and K⁺ salts are usually applied together as fertilizers, the binary K→NH₄ exchange of two benchmark Botswana soils, Pellustert and a Haplustalf, was studied to determine the selectivity coefficients and the thermodynamic exchange constant with special reference to N economy. The Vanselow and the Gaines and Thomas coefficients indicated preference for NH₄⁺ by the Pellustert and K by the Haplustalf across the exchanger phase composition. The equilibrium constant (K_ex) was 1.807 for the Pellustert and 0.174 for the Haplustalf. The exchange free energy (ΔG_ex⁰) was ?1.467 kJ mol^?1 for the Pellustert and 4.334 kJ mol^?1 for the Haplustalf. Negative ΔG_ex⁰ for the Pellustert is consistent with preference for NH₄⁺ to K⁺ in contrast to positive ΔG_ex⁰ for the Haplustalf. The greater stability of NH₄X than KX complex in the Pellustert, and KX than NH₄X in the Haplustalf, would mean increased residence time of NH₄⁺ in the Pellustert than the Haplustalf. The implication of short residence time of NH₄⁺ in soil is rapid nitrification, thereby leading to NO₃^??N leaching losses and possible groundwater contamination.     

Calcium-Ammonium Selectivity of Two Benchmark Soils from Botswana as Assessed by Competing Semi-empirical Ion Exchange Equations

The effectiveness of lime-ammonium-nitrate (LAN) as a nitrogen (N) fertilizer in weathered soils depends on the respective selectivity for ammonium (NH₄) and calcium (Ca) by the soils. The study assessed Ca²⁺/NH₄⁺ exchange selectivity of two benchmark soils from Botswana and examined the soil fertility management implications. Surface horizons (0–20 cm) of Pellustert and Haplustalf were equilibrated with 50 ml stock solution containing variable concentrations of Ca²⁺ and NH₄⁺. The Ca²⁺/NH₄⁺ exchange data were fitted into the Vanselow (K_V), Gaines and Thomas (K_GT), Davies (K_D), and the regular solution (K_RS) equations. The selectivity coefficients for the Ca²⁺/NH₄⁺ exchange reactions varied widely with the soil exchanger composition except for the relatively stable K_RS. The selectivity coefficients indicated strong preference for NH₄⁺ to Ca²⁺. The thermodynamic exchange constant, K_ex, was 5.75 ± 1.24 in the Pellustert, indicating preferential adsorption of NH₄⁺, but not in the Haplustalf with K_ex = 0.92 ± 0.27. The free energy for Ca²⁺/NH₄⁺ exchange (ΔG°_ex) was negative (?4.26 ± 0.59 kJ mol^?1) in the Pellustert but slightly positive in the Haplustalf (0.34 ± 0.87 kJ mol^?1). In conclusion, the soil-NH₄ complex was more stable than soil-Ca complex in the Pellustert, indicating LAN as a N fertilizer would have greater potential effectiveness in the Pellustert than in the Haplustalf.     

Influence of alkaline particulates on the chemistry of fog water at Delhi,North India

Chemical analysis of fog water collected by impaction in a pre-cooled chamber in Delhi has shown high concentrations of major ions. The dominant ions measured were Na⁺, K⁺, Ca⁺², and Mg⁺². The concentrations of acidic ions, SO₄ ^?2 and NO₃ ^?, were low. The pH values in the fog water were highly alkaline and varied from 6.4 to 7.6. The high concentrations of soil-oriented components, especially Ca⁺², were more than sufficient to neutralize the small acidity in the fog water and were responsible for maintaining high alkaline pH. The pH values of fog water did not attain the low values in India (Delhi), as found in other polluted environments of Europe and the northeast United States.     

Effects of Supplemental Calcium on Ion Accumulation,Transport and Plant Growth of Salt Sensitive Brassica Rapa Landrace

ABSTRACT

Effects of three supplemental calcium (Ca⁺⁺; 2.5, 5.0, and 10 mole m^?3) concentrations on ion accumulation, transport, selectivity, and plant growth of salt-sensitive species, Brassica rapa ‘Sani’ in saline medium were investigated. Supplemental Ca⁺⁺ in the presence of 125 mol m^?3 sodium chloride (NaCl) did not improve the dry weight and leaf area indicating no role played by Ca⁺⁺ in the alleviation of salinity induced growth inhibition. However, calcium chloride (CaCl₂) did significantly affect sodium (Na⁺), potassium (K⁺), and Ca⁺⁺ contents of roots and shoots. The ion contents of shoots were significantly greater than those of roots per g dry weight, indicating ion transportation to shoots is greater than ion accumulation in roots. Use of CaCl₂ in 125 mol m^?3 NaCl reduced the Na⁺ content but increased K⁺ and Ca⁺⁺ contents in shoots. Sodium contents in shoots differed among the supplemental Ca⁺⁺ treatments indicating the role of CaCl₂ in Na⁺ ions transportation. Calcium content in shoots declined significantly in the control treatment (0 CaCl₂) but increased significantly in 10 mol m^?3 CaCl₂. The root also showed the effects of Ca⁺⁺ on the reduction of Na⁺ content and the increase of K⁺ and Ca⁺⁺ content. Unexpectedly, 5 mol m^?3 CaCl₂ induced the highest Na⁺ content in roots at 16 days after treatment. Supplemental CaCl₂ application influenced the K⁺ or Ca⁺⁺ selectivity over Na⁺ in two ways, ion accumulation at roots and transport to shoots. However, high CaCl₂ treatments allowed greater Ca⁺⁺ selectivity over Na⁺ than low CaCl₂. Likewise, high supplemental CaCl₂ showed higher K⁺ selectivity over Na⁺ than low CaCl₂. A marked increase in K⁺ versus Na⁺ selectivity for the transport process occurred at 10 mol m^?3 CaCl₂ treatments. The roots and shoots exhibited higher K⁺/Na⁺ and Ca⁺⁺/Na⁺ ratios in high CaCl₂ treatment than in low. The results are discussed in context to supplemental Ca⁺⁺ concentrations, ions accumulation, transportation and selectivity of salt sensitive Brassica rapa cultivar.     

Exchange equilibria of potassium in soils. II. Effect of farmyard manure on K-Mg exchange

Exchange behaviour of potassium versus magnesium was studied on surface soil samples of 3 Ustochrepts from a semiarid tropical region in relation to different levels of cattle farmyard manure (FYM, 0, 2.5, 5 and 10%). Magnesium saturated soil samples were equilibrated with KCl + MgCl₂ solutions having a range of equivalent ion fraction of K from 0 to 1 in the equilibrium solutions. The experimental results were analysed and interpreted, using different exchange selectivity quotients and thermodynamic parameters. Application of FYM caused a small but consistent increase in the K-preference over Mg as depicted from the normalized exchange isotherms. Standard free energy of K-Mg exchange were strongly negative (ΔGo-6.97 to ?9.47 kJ eq^?1 by Gaines and Thomas approach; ΔG'o ?10.85 to ?14.15 kJ M^?1 by Babcock and Duckart approach), suggesting a strong thermodynamic preference for K over Mg in these soils. For comparable treatments, ΔGo were about ?0.84 to ?1.25 kJ eq^?1 more negative for K-Mg, compared to K-Ca system reported earlier. ΔGo for 10% FYM treatments became more negative over the controls by 2.34, 1.40 and 0.53 kJ eq^?1 for Hissar, Panipat and Pehowa soils, respectively. All the selectivity quotients scrutinized in this investigation, viz., Gapon (K_G), Vanselow (K_v) and thermodynamic (K_N) were strongly K-saturation dependent; the dependence becoming more pronounced with the addition of FYM.     

Importance of plasmalemma ATPase in the retention and exclusion of inorganic ions

The experiments were focused on the question whether the plasmalemma ATPase activity (proton pump) has an influence on the efflux of major inorganic ion species. Efflux from roots of intact Trifolium pratense, Hordeum vulgare, Glycine max, and Zea mays was examined into a solution containing 100 μM CaCl₂ and 500 μM NH₄⁺ as sulfate in the control solution and 100 μM CaCl₂ and 500 μM NH₄⁺ as vanadate in the test solution. Vanadate being an inhibitor of the plasmalemma ATPase depressed significantly the H⁺ secretion of roots into the outer solution but had no major impact on the efflux of cation species. In the presence of vanadate significantly higher amounts of sulfate, phosphate, and nitrate were released into the outer solution by roots of soya and maize as compared with the control treatment (no vanadate). In the absence of vanadate, virtually no nitrate was released by all species examined whereas in the vanadate treatment significant amounts of NO₃^? were released. Vanadate inhibited the uptake of Cl^? in barley and maize and increased the uptake of Ca²⁺ in soya. It is concluded that the plasmalemma ATPase activity plays a major rule in the “ionic stat” of cells in providing protons to the apoplast for the reabsorption of sulfate, phosphate, and particularly nitrate which have leaked out of the cytosol.     

Exploring the effect of organic matter on the interactions between mineral particles and cations with Wien effect measurements

Purpose

Understanding of the interactions between cations, mineral particles, and organic matter (OM) in soils is of paramount importance in plant nutrition and environmental science, and thus, these phenomena have been studied extensively. At present, an effective and simple tool to investigate these interactions does not exist. Based on previous studies of Wien effect in suspensions, the interactions of cations with soil mineral particles, complicated by the presence of organic matter, can be easily determined by means of Wien effect measurements, which was the objective of this study.

Materials and methods

A paddy soil originating from a yellow-brown soil, rich in organic matter, served as a test sample, from which the clay fraction of less than 2 μm in diameter was separated. Organic matter of aliquots of the clay fraction was removed by the oxidation with hot H₂O₂, and the natural and OM-free samples were saturated with various cations: Na⁺, K⁺, Ca²⁺, and Cd²⁺. The effects of OM present in the paddy soil on the interactions between the cations and the soil mineral particles were investigated by measuring the suspension Wien effect with a homemade apparatus, SHP-2.

Results and discussion

The weak electrical field electrical conductivities (EC₀) of suspensions of the natural soils saturated with various cations were higher than those of the OM-free soils. The rate of increase in electrical conductivity of suspensions of the OM-free soil, except that of suspensions saturated with Na⁺, at electrical field strengths >50～100 kV?cm^?1 was higher than those of the natural soil suspensions. The presence of OM increased the mean free binding energies of cations other than Na⁺. The increasing binding energies for K⁺ and Ca²⁺ were 0.56 and 0.57 kJ?mol^?1, respectively, which were significantly larger than the increase for Cd²⁺ as only 0.03 kJ?mol^?1. The binding energies of various cations on both natural and OM-free soils were all in the order: Na⁺?<?K⁺?<?Ca²⁺≈Cd²⁺. As opposed to its effect on the binding energies, the presence of OM reduced the mean free adsorption energies of the cations. Except for Na⁺, the adsorption energies of K⁺, Ca²⁺, and Cd²⁺ at field strengths >50 kV?cm^?1 were lower in the natural soil as compared with the OM-free soil, and the differences between the adsorption energies became larger with increasing field strengths. The presence of OM made the zeta potential of the soil particles saturated with Na⁺ and K⁺ positive, and the particles saturated with Ca²⁺ and Cd²⁺ negative.

Conclusions

Organic matter affected the interactions of cations with soil mineral particles significantly. Binding and adsorption energies, which were quantitative measures of the interactions between cations and soil particles, could be determined by Wien effect measurements in suspensions. The binding energies on natural soils were larger than those on the corresponding OM-free soils, and the adsorption energies on the natural soils were lower than those on OM-free soils.     

The Odd–Even Behaviour of Dicarboxylic Acids Solubility in the Atmospheric Aerosols

The solubility and the enthalpy of dicarboxylic acids have been determined in water at intervals between 278.5 and 543.5 K. At 298.15 K, the values derived were: Δ_sol H _m (m?=?1.33 mol kg^?1)?=?29.80 kJ mol^?1for oxalic acid; Δ_sol H _m (m?=?16.03 mol kg^?1)?=?12.82 kJ mol^?1 for malonic acid; Δ_sol H _m (m?=?0.75 mol kg^?1)?=?28.20 kJ mol^?1 for succinic acid; Δ_sol H _m (m?=?8.77 mol kg^?1)?=?48.01 kJ mol^?1 and Δ_sol H _m (m?=?0.17 mol kg^?1)?=?40.30 kJ mol^?1 for glutaric and adipic acid respectively. The solubility value exhibits a prominent odd–even effect with respect to terms with even number of carbon atoms with the odd carbon numbers showing much higher solubility. Observations made in the atmospheres suggest that this odd–even effect may have implications for the relative abundance of these acids in aerosols.     

SPECIFIC ION EFFECTS ON THE SEED GERMINATION OF SUNFLOWER

Salinity can affect germination of seeds either by creating osmotic potentials that prevent water uptake or by toxic effects of specific ions. This work was carried out to evaluate the germination of sunflower (Helianthus annuus L.) seeds under increasing salinity by using the most abundant salts in China. Potassium (K⁺), sodium (Na⁺), and calcium (Ca²⁺) contents in hypocotyls were determined on the fifth day. At same concentration of salt solution, the adverse effect of ions is in the following sequence: carbonate radical (CO₃ ^2?) > sulfate radical (SO₄ ^2?), chloride (Cl^?) > bicarbonate radical (HCO₃ ^?), magnesium (Mg²⁺) > Ca²⁺, and Na⁺ > K⁺. The effect of salinity on the germination phase of development is mainly due to its osmotic component other than the ion toxicity. Calcium decreased as increasing of the concentration of salt solutions, and cannot act as the role of enhancing cell division and membrane permeability.     

MODELING GROWTH AND ION CONCENTRATION OF LILIUM IN RESPONSE TO NITROGEN:POTASSIUM:CALCIUM MIXTURE SOLUTIONS

Nutrient solution composition plays an important role in root uptake rate due to interactions among nutrients and internal regulation. Studies to determine the optimum nutrient solution concentration are focused on individual ions, ignoring the adaptation mechanisms triggered by plants when growing in a varying external nutrient concentration. The objective of the present study was to determine the response in growth and tissue ion concentration of lilium cv. ‘Navona’ to nutrient mixtures of varying proportions of nitrogen (N), potassium (K⁺), and calcium (Ca²⁺) in solution using mixture experiments methodology in order to determine the optimum concentration. Bulbs of lilium were transplanted in plastic crates and drip-irrigated with the treatment solutions, which consisted of a mixture of N, K⁺, and Ca²⁺ whose total concentration was 340 mg L^?1 and minimum concentrations of each ion was 34 mg L^?1. Chlorophyll concentration (SPAD), shoot fresh weight (FW), leaf FW, and leaf area were measured 60 days after transplanting and ion analysis was performed on shoot tissues from selected treatments. Lilium exhibited a moderate demand for N and K⁺ (136–170 mg L^?1 N and 116–136 mg L^?1 K⁺) and a very low demand for Ca²⁺ (34–88 mg · L^?1). This low demand may be due to the remobilization of the nutrients stored in the bulbs. Integrating the predictions of the models estimated to produce >90% of maximum growth, the optimum nutrient solution should contain Ca²⁺ at a concentration between 34 and 126 mg · L^?1, K⁺ between 119 and 211 mg · L^?1, and N between 92 mg · L^?1 and 211 mg · L^?1. Increasing external N concentration affected internal N concentration but not internal K⁺ or Ca²⁺ concentrations, despite that the increase in external N was associated with a decrease in external K⁺ and Ca²⁺. Similar trends were observed for external K⁺ and Ca²⁺ concentration. In conclusion, lilium was able to maintain a relatively constant K⁺ and Ca²⁺ concentration regardless of the lower concentration in the nutrient solution when N was increased (similar response was observed for K⁺ and Ca²⁺) and it has a low Ca²⁺ demand and moderate N and K⁺ supply.     

THE POTASSIUM STATUS OF MALAWI SOILS

Twenty surface soils from four main Soil Groups in Malawi and their sub-soils were divided into three groups based on cation exchange capacity (group I, CEC < 50; group II, 50–100; and group III > 100μeq g^–1). In each soil group the maximum amounts of K removed by successive extraction with 0.005 M CaCl₂ solution were well related to the potassium potential pK–0.5p(Ca + Mg), exchangeable K, ‘step K’, and the quotient ‘step K’/CR.K, where CR.K is ‘constant-rate’potassium. In Group III soils only, ‘step K’/CR.K values were significantly correlated with pH, clay, and CEC, and this suggested that the soils were relatively rich in K⁺ specific binding sites. In 27 soils from an NPK factorial experiment on tea, the rate of depletion of extractable K reserve increased with ammonium sulphate treatment, whereas K fertilizers tended to off-set significantly (P= 0.001) the depletion of K reserve. The values for the change in free energy ΔG =RT In a_K/ (a_(Ca+Mg)) ^½, ranged from –12 to –16 kJ mol^–1, and field observations showed that tea plants growing on soils having ΔG values less than –15 kJ mol^–1 responded to K fertilizers. The investigation has indicated that heavily cropped soils are likely to show crop responses if the intensive cropping system does not include supplementation of K.     

Soil Solution as Affected by Plant Residues and Nitrogen Rates

Cation mobility in acidic soils with low organic‐matter contents depends not only on sorption intensity but also on the solubility of the species present in soil solution. In general, the following leaching gradient is observed: potassium (K⁺) > magnesium (Mg²⁺) > calcium (Ca²⁺) > aluminum (Al³⁺). To minimize nutrient losses and ameliorate the subsoil, soil solution must be changed, favoring higher mobility of M²⁺ (metal ions) forms. This would be theoretically possible if plant residues were kept on the soil surface. An experiment was conducted in pots containing a Distroferric Red Latosol, with soil solution extractors installed at two depths. Pearl millet, black oat, and oilseed radish residues were laid on the soil surface, and nitrogen (as ammonium nitrate) was applied at rates ranging from 0 to 150 mg kg^?1. Corn was grown for 52 days. Except for K⁺ and ammonium (NH₄ ⁺), nitrogen rates and plant residues had little effect upon the concentrations and forms of the elements in the soil solution. Presence of cover crop residues on soil surface decreased the effect of nitrogen fertilizer on Ca leaching. More than 90% of the Ca²⁺, Mg²⁺, and K⁺ were found as free ions. The Al³⁺ was almost totally complexed as Al(OH₃)⁰. Nitrogen application increased the concentrations of almost all the ions in soil solution, including Al³⁺, although there was no modification in the leaching gradient.     

Observation of specific ion effects in humus aggregation process

Specific ion effects play a vital role in a variety of colloidal and interfacial processes. However, few studies have reported the specific ion effects in the humus aggregation process, which strongly influence the transport and fate of environmental pollutants. In this study, soil humus colloids were prepared and characterized, and the specific ion effects on humus aggregation in electrolyte solutions were investigated at a variety of concentrations and p H values using dynamic light scattering methods. Activation energy(?E), which is known to reflect the dynamics and stability of a colloidal system, was used to quantitatively characterize the specific ion effects. The results showed that given ?E value of 2.48 × 10~3 J mol~(-1) at p H 3.0, the electrolyte concentrations were 91.6, 58.2, 3.8, and 0.8 mmol L~(-1) for Na~+, K~+, Mg~(2+), and Ca~(2+), respectively, thus indicating significant specific ion effects in the humus aggregation process. Most importantly, decreasing the electrolyte concentrations increased the differences in the ?E value between two cation species with the same valence(i.e., ?EN_a-?E_K and ?E_(Mg)-?E_(Ca)), while increasing the p H increased the magnitude of ?E_(Mg)-?E_(Ca). However, the classic Derjaguin,Landau, Verwey, and Overbeek(DLVO) theory and the double layer theory, as well as the currently widely used ionic hydration and dispersion effects, failed to predict the experimentally observed increase in the specific ion effects with decreasing electrolyte concentrations in a quantitative sense. These results have implications for the necessity of involving specific ion effects for a better understanding of humus aggregation and interactions in aqueous and soil systems.     

Effect of 15-Year-Long Fertilization on Potassium Quantity/Intensity Relationships in Black Soil in Northeastern China

The effect of long-term fertilization and cropping on soil potassium (K)–supplying capacity has not been extensively studied. Five treatments [control, nitrogen (N), N–potassium (P), NPK, and NPK + manure (NPKM)] were used to evaluate the quantity and intensity relationship (Q/I) of K in black soil (Luvic Phaeozems soil) after a 15-year (1990–2005) long-term fertilization with a continuous corn cropping located in Changchun, Jilin Province, northeast China. Results showed that the long-term K fertilization of NPK or NPKM markedly increased the values of equilibrium active ratio (AR₀ ^K) and nonspecifically available K (?ΔK₀) but decreased the potential buffering capacity (PBC^K) value. Values of the AR₀ ^K and??ΔK₀ in the NPK and NPKM treatment were about four and two times greater than those in the control, N, and NP treatments, respectively. Compared with the non-K fertilization, PBC^K values were decreased by 40–49% under the K fertilization. The black soil suffered from K deficiency even with NPK fertilization as evidenced from the greater free energies of K⁺ exchanging for calcium (Ca²⁺) and magnesium (Mg²⁺) (?ΔG) (14.7–18.8 kJ mol^?1) than the threshold value of 14.6 kJ mol^?1, from the lower soil K⁺ saturation (1.34%–1.44%) than the critical value of 2.00%, and from the response of corn yield to K fertilization. Our results demonstrated that the increment of the current K application rate through fertilizer and/or manure is needed to improve corn yield in the long run in northeastern China.     

Effects of Land Use on Hydrochemistry and Contamination of Karst Groundwater from Nandong Underground River System, China

The Nandong Underground River System (NURS) is located in Southeast Yunnan Province, China. Groundwater in NURS plays a critical role in socio-economical development of the region. However, with the rapid increase of population in recent years, groundwater quality has degraded greatly. In this study, the analysis of 36 groundwater samples collected from springs in both rain and dry seasons shows significant spatial disparities and slight seasonal variations of major element concentrations in the groundwater. In addition, results from factor analysis indicate that NO ₃ ^? , Cl^?, SO ₄ ^2? , Na⁺, K⁺, and EC in the groundwater are mainly from the sources related to human activities while Ca²⁺, Mg²⁺, HCO ₃ ^? , and pH are primarily controlled by water–rock interactions in karst system with Ca²⁺ and HCO ₃ ^? somewhat from anthropogenic inputs. With the increased anthropogenic contaminations, the groundwater chemistry changes widely from Ca-HCO₃ or Ca (Mg)-HCO₃ type to Ca-Cl (+NO₃) or Ca (Mg)-Cl (+NO₃), and Ca-Cl (+NO₃+SO₄) or Ca (Mg)-Cl (+NO₃+SO₄) type. Concentrations of NO ₃ ^? , Cl^?, SO ₄ ^2? , Na⁺, and K⁺ generally show an indistinct grouping with respect to land use types, with very high concentrations observed in the groundwater from residential and agricultural areas. This suggests that those ions are mainly derived from sewage effluents and fertilizers. No specific land use control on the Mg²⁺ ion distribution is observed, suggesting Mg²⁺ is originated from natural dissolution of carbonate rocks. The distribution of Ca²⁺ and HCO ₃ ^? does not show any distinct land use control either, except for the samples from residential zones, suggesting the Ca²⁺ and HCO ₃ ^- mainly come from both natural dissolution of carbonate rocks and sewage effluents.     

Diurnal Macronutrients Uptake Patterns by Lettuce Roots under Various Light and Temperature Levels

In order to reduce nutrient wastes to the environment the supply should be in accordance to the demand for these. Two experiments were conducted to study and quantify the effect of temperature, irradiance, and plant age on the uptake of nitrate (NO₃^?), ammonium (NH₄⁺), dihydrogen phosphate ion (H₂PO₄^?), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), and sulfate (SO₄²). In the first experiment, various levels of temperature and irradiance were applied to plants in a growth chamber, while in the second experiment the uptake was studied along the crop season under greenhouse conditions. The uptake rates were calculated at 2-hour intervals through sampling the nutrient solution and analyzing it by inductively coupled plasma atomic emission spectrometry (ICP-AES). Increasing light and temperature enhance the uptake rates, while the rates decrease with plant age. Nitrogen absorption was similar during the day as during the night. No differences were found in the absorption of H₂PO₄^?, K⁺, Ca²⁺, Mg²⁺, and SO₄^2? between day and night. Nitrate absorption was found to have a positive correlation with the absorption of all the ions except for NH₄⁺.     

不同白榆品系对滨海盐碱地的改良效果及盐分离子的分布与吸收

为揭示不同白榆(Ulmus pumila L.)品系对滨海盐碱地土壤盐分的改良作用及盐分离子在土壤-白榆系统中的分布与吸收特征,筛选适宜在滨海盐碱地造林的耐盐白榆品系,以中度盐渍化生境下4年生的6种白榆品系(1,5,28,30,46,105号)为试验材料,采用野外取样与室内测试相结合的方法,研究了Na+、K+、Ca2+、Mg2+等盐离子在土壤及白榆品系各器官(根、茎、叶)中的分布特征。结果表明:(1)白榆可降低滨海盐碱地土壤中盐离子及全盐含量,不同白榆品系较对照的土壤全盐含量降低了55.0%～63.1%,30号白榆降幅最大。(2)不同白榆品系将Na+、K+、Ca2+、Mg2+优先积累到叶中,且叶中维持较高的K+/Na+、Ca2+/Na+、Mg2+/Na+比值,不同白榆品系通过建立新的离子平衡以适应盐胁迫环境。(3)不同白榆品系的离子吸收选择性系数均为SK,NaSCa,NaSMg,Na,其对K+的吸收选择性大于对Ca2+、Mg2+吸收选择性;种内差异导致不同白榆品系对Na+、K+、Ca2+、Mg2+吸收选择能力不同,28号白榆根系对K+的吸收性最强,5号白榆根系对Ca2+、Mg2+的吸收性最强。     

Solubility and Stability of Calcium Arsenates at 25∘C

The solubility and stability of calcium arsenates at 25 ^°C was determined by both precipitation and dissolution experiments. Ca₃(AsO₄)₂? 3H₂O(c), Ca₃(AsO₄)₂? 2¹/₄H₂O(c), Ca₅(AsO₄)₃(OH)(c) and Ca₄(OH)₂(AsO₄)₂? 4H₂O(c) were identified in our experiment over a wide range of pH and for Ca/As molar ratios between 1.25 and 4.0. The solids precipitated at pH = 3 ～ 7 and Ca/As = 1.5 were phase-pure and well-crystallized Ca₃(AsO₄)₂? xH₂O(c) and had relatively larger grain size than those formed at pH > 7. Based on the analytical results and using the computer program PHREEQC, the solubility products for Ca₃(AsO₄)₂? 3H₂O(c), Ca₃(AsO₄)₂? 2¹/₄H₂O(c), Ca₅(AsO₄)₃(OH)(c) and Ca₄(OH)₂(AsO₄)₂? 4H₂O(c) were calculated as K _sp of 10^{? 21.14}(10^{? 20.01} ～ 10^{? 22.02}), 10^{? 21.40}(10^{? 20.08} ～ 10^{? 21.98}), 10^{? 40.12}(10^{? 37.53} ～ 10^{? 42.72}) and 10^{? 27.49}(10^{? 26.10} ～ 10^{? 28.91}), respectively. Correspondingly, the free energies of forming (Δ G _f ^o ) of these calcium arsenates were calculated to be ?3787.87 kJ/mol, ?3611.50 kJ/mol, ?5096.47 kJ/mol and ?4928.86 kJ/mol.     

Factors Influencing the Dissolution of Phosphate Rock in a Range of High P‐Fixing Soils from Cameroon

Abstract

A laboratory incubation experiment was conducted to evaluate the soil factors that influence the dissolution of two phosphate rocks (PRs) of different reactivity (Gafsa, GPR, reactive PR; and Togo‐Hahotoe, HPR, low reactivity PR) in seven agricultural soils from Cameroon having variable phosphorus (P)‐sorption capacities, organic carbon (C) contents, and exchangeable acidities. Ground PR was mixed with the soils at a rate of 500 mg P kg^?1 soil and incubated at 30°C for 85 days. Dissolution of the PRs was determined at various intervals using the ΔNaOH‐P method (the difference of the amount of P extracted by 0.5 M NaOH between the PR‐treated soils and the control). Between 4 and 27% of HPR and 33 and 50% of GPR were dissolved in the soils. Calcium (Ca) saturation of cation exchange sites and proton supply strongly affected PR dissolution in these soils. Acid soils with pH‐(H₂O)<5 (NKL, ODJ, NSM, MTF) dissolved more phosphate rock than those with pH‐(H₂O)>5 (DSC, FGT, BAF). However, the lack of a sufficient Ca sink in the former constrained the dissolution of both PRs. The dissolution of GPR in the slightly acidic soils was limited by increase in Ca saturation and that of HPR was constrained by limited supply in protons. Generally, the dissolution of GPR was higher than that of HPR for each soil. The kinetics of dissolution of PR in the soils was best described by the power function equation P=At^B. More efficient use of PR in these soils can be achieved by raising the soil cation exchange capacity, thereby increasing the Ca sink size. This could be done by amending such soils with organic materials.