Changes in Retrogradation Properties of Rice Starches with Amylose Content and Molecular Properties

The increases in storage modulus (G′), retrogradation enthalpy change (ΔH) and ΔH‐related Avrami kinetic parameters of gelatinized rice starch dispersions at 25% (w/w) were investigated with respect to storage period, amylose content (AC), and molecular properties. Three high‐AC and five low‐AC rice cultivars were compared for understanding the multiple influences of AC and molecular properties involved. After refining the results of correlation analysis, the G′ of just‐cooled samples changed positively, mainly with AC and additionally with the average chain length of amylose (CL_AM) and the weight ratio of extra‐long plus long chains to short chains of amylopectin (AP) (r_APchain). The developed ΔH on short‐term storage (10 days) elevated with increasing AC and CL_AM and decreasing degree of polymerization of AP (DP_AP), but after long‐term aging for one to three months with increasing r_APchain, especially for the low‐AC cultivars examined. Greater Avrami rate constants for retrogradation could be attributed to the combination of a lower DP_AP and r_APchain or AP chain length and a greater CL_AM. The polynomials using these critical factors to describe the retrogradation parameters were elucidated and could account for 85–99.6% of data deviations.     

Gelatinization and Retrogradation Kinetics of High‐Fiber Wheat Flour Blends: A Calorimetric Approach

The impact of dietary fiber (DF) mixtures on dough thermal properties needs to be investigated when designing high‐fiber wheat bread. Effects of flour replacement at different levels (6–34%) by soluble (inuline [FN]), partially soluble (sugar beet [FX], pea cell wall [SW]), and insoluble (pea hull [EX]) DF on wheat dough thermal profiles have been investigated by simulating baking, cooling, and storage in differential scanning calorimetry (DSC) pans. In general, DF incorporation into water‐flour systems delayed endothermic transition temperatures for both gelatinization and retrogradation phenomena except for the peak temperature (T_p) of retrogradation. With some exception, the pattern of the enthalpy of amylopectin retrogradation was lower and slower (lower constant of proportion, k) over 10 days of storage in gelatinized hydrated flour‐fiber blends when compared with control without DF. FX, a partially soluble fiber, provided major effects on gelatinization (T_p decrease and ΔH increase) and retrogradation kinetics (the Avrami exponent, n, increase). Single presence of EX allowed a significant reduction in the Avrami exponent n leading to slower kinetics for amylopectin retrogradation when included in the blends.     

A field trial to evaluate the pollution potential to ground and surface waters from woodchip corrals for overwintering livestock outdoors

Outwintering beef cattle on woodchip corrals offers stock management, economic and welfare benefits when compared with overwintering in open fields or indoors. A trial was set up on a loamy sand over sand soil to evaluate the pollution risks from corrals and the effect of design features (size and depth of woodchips, stocking density, and feeding on or off the corral). Plastic‐lined drainage trenches at 9–10 m spacing under the woodchips allowed sampling of the leachate. Sampling of the soil to 3.6 m below the corral allowed evaluation of pollutant mitigation during vadose zone transport. Mean corral leachate pollutant concentrations were 443–1056 mg NH₄‐N L^?1, 372–1078 mg dissolved organic carbon (DOC) L^?1, 3–13 mg NO₃‐N L^?1, 8 × 10⁴–1.0 × 10⁶Escherichia coli 100 mL^?1 and 2.8 × 10²–1.4 × 10³ faecal enterococci 100 mL^?1. Little influence of design features could be observed. DOC, NH₄ and (in most cases) E. coli and faecal enterococci concentrations decreased 10²–10³ fold when compared with corral leachate during transport to 3.6 m but there were some cores where faecal enterococci concentrations remained high throughout the profile. Travel times of pollutants (39–113 days) were estimated assuming vertical percolation, piston displacement at field moisture content and no adsorption. This allowed decay/die‐off kinetics in the soil to be estimated (0.009–0.044 day^?1 for DOC, 0.014–0.045 day^?1 for E. coli and 0–0.022 day^?1 for faecal enterococci). The mean [NO₃‐N] in pore water from the soil cores (n = 3 per corral) ranged from 114 ± 52 to 404 ± 54 mg NO₃‐N L^?1, when compared with 59 ± 15 mg NO₃‐N L^?1 from a field overwintering area and 47 ± 40 mg NO₃‐N L^?1 under a permanent feeding area. However, modelling suggested that denitrification losses in the soil profile increased with stocking density so nitrate leaching losses per animal may be smaller under corrals than for other overwintering methods. Nitrous oxide, carbon dioxide and methane fluxes (measured on one occasion from one corral) were 5–110 g N ha^?1 day^?1, 3–23 kg C ha^?1 day^?1, and 5–340 g C ha^?1 day^?1 respectively. Ammonia content of air extracted from above the woodchips was 0.7–3.5 mg NH₄‐N m^?3.     

The concentrations of fatty acids in organo-mineral particle-size fractions of a Chernozem

Fatty acids, the most abundant class of soil lipids, indicate pedogenetic processes and soil management. However, their quantitative distribution in organo‐mineral particle‐size fractions is unknown. The concentrations of n‐C_10:0 to n‐C_34:0 fatty acids both in whole soil samples and in the organo‐mineral particle‐size fractions of the Ap horizon of a Chernozem were determined (i) to evaluate the effects of long‐term fertilization and (ii) to investigate their influence on the aggregation of organo‐mineral primary particles. Quantification by gas chromatography/mass spectrometry (GC/MS) showed that long‐term fertilization with nitrogen, phosphorus and potassium (NPK) and farmyard manure (FYM) led to larger concentrations (25.8 µg g^?1) of fatty acids than in the unfertilized sample (22.0 µg g^?1). For particle‐size fractions of the unfertilized soil, the fatty acid concentrations increased from the coarse silt to the clay fractions (except for fine silt). Fertilization with NPK and FYM resulted in absolute enrichments of n‐C_21:0 to n‐C_34:0 fatty acids with a maximum at n‐C_28:0 in clay (×2.2), medium silt (×2.0), coarse silt (×1.8) and sand (×2.9) compared with the unfertilized treatment (the factors of enrichment are given in parentheses). New evidence for the aggregate stabilizing function of n‐C_21:0 to n‐C_34:0 fatty acids was shown by the characteristic pattern in size‐fractionated, disaggregated and aggregated samples. Highly significant correlations of fatty acid concentrations with organic C concentrations and specific surface areas are interpreted as indicators of (i) trapping of fatty acids in organic matter macromolecules and (ii) direct bonding to mineral surfaces. This interpretation was supported by the thermal volatilization and determination of fatty acids by pyrolysis‐field ionization mass spectrometry (Py‐FIMS).     

Molecular and Gelatinization Properties of Rice Starches from IR24 and Sinandomeng Cultivars

The differences in pasting properties involving gelatinization and retrogradation of rice starches from IR24 and Sinandomeng cultivars during heating‐cooling processes were investigated using a Rapid Visco Analyser (RVA)and a dynamic rheometer. The results were discussed in relation to the molecular structure, actual amylose content (AC), and concentration of the starches. Generally, both starches possessed a comparable AC (≈11 wt%), amylose average chain length (CL), iodine absorption properties, and dynamic rheological parameters on heating to 95°C at 10 wt% and on cooling to 10°C at higher concentrations. In contrast to Sinandomeng, IR24 amylose had a greater proportion of high molecular weight species and number‐average degree of polymerization (DP_n). IR24 amylopectin possessed a lower DP_n and greater CL, exterior CL (ECL), and interior CL (ICL). Comparing the results of RVA analysis and dynamic rheology, the gelatinization properties and higher retrogradation tendencies of IR24 starch can be related to the structural properties and depend on starch concentration. In addition, the exponent n of starch concentration for storage moduli at 25°C (G′₂₅ ∝ Cⁿ) increased linearly with increasing AC.     

Kinetic behaviour of alkaline phosphatase desorbed from different clay minerals

The kinetic (K_m, V_max) 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 K_m and V_max were measured in the extract, the remaining sediment and in the whole set-up. With kaolinite and illite, V_max of the desorbed AP was lower than that of the sediment. However, with montmorillonite, V_max of AP in the extract and whole system increased if compared to the control, but decreased in the sediment. The K_m 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.     

Retrogradation of du wx and su2 wx Maize Starches After Different Gelatinization Heat Treatments

Retrogradation of du wx and su2 wx starches after different gelatinization heat treatments was studied by differential scanning calorimetry. Suspensions of 30% (w/w) starch were initially heated to final temperatures of 55–180°C. Gelatinized starch was cooled and stored at 4°C. Starch retrogradation in the storage period was influenced by initial heat treatments. Retrogradation of du wx starch was rapid: when initially heated to 80–105°C, retrogradation enthalpy was ≈10 J/g after one day at 4°C. The retrogradation enthalpy was ≈15 J/g after 22 days of storage, and reached a maximum of 16.2 J/g after 40 days of storage. For du wx starch, application of the Avrami equation to increases in retrogradation enthalpy suggests retrogradation kinetics vary with initial heating temperature. Furthermore, starch retrogradation may not fit simple Avrami theory for initial heating ≤140°C. Retrogradation of su2 wx starch was slow. After 30 days of storage at 4°C, the maximum retrogradation enthalpy for all initial heating temperatures tested was 7.0 J/g, for the initial heating to 80°C. This work indicates that gelatinization heat treatment in these starches is an important factor in amylopectin retrogradation, and that the effect of initial heat treatment varies according to the genotype.     

Quantification of long‐chain fatty acids in dissolved organic matter and soils

The objective was to develop and adapt a versatile analytical method for the quantification of solvent extractable, saturated long‐chain fatty acids in aquatic and terrestrial environments. Fulvic (FA) and humic (HA) acids, dissolved organic matter (DOM) in water, as well as organic matter in whole soils (SOM) of different horizons were investigated. The proposed methodology comprised extraction by dichloromethane/acetone and derivatization with tetramethylammonium hydroxide (TMAH) followed by gas chromatography/mass spectrometry (GC/MS) and library searches. The C_10:0 to C_34:0 methyl esters of n‐alkyl fatty acids were used as external standards for calibration. The total concentrations of C_14:0 to C_28:0 n‐alkyl fatty acids were determined in DOM obtained by reverse‐osmosis of Suwannee river water (309.3 μg g^—1), in freeze‐dried brown lake water (180.6 μg g^—1), its DOM concentrate (93.0 μg g^—1), humic acid (43.1 μg g^—1), and fulvic acid (42.5 μg g^—1). The concentrations of the methylated fatty acids (n‐C_16:0 to n‐C_28:0) were significantly (r² = 0.9999) correlated with the proportions of marker signals (% total ion intensity (TII), m/z 256 to m/z 508) in the corresponding pyrolysis‐field ionization (FI) mass spectra. The concentrations of terrestrial C_10:0 to C_34:0 n‐alkyl fatty acids from four soil samples ranged from 0.02 μg g^—1 to 11 μg g^—1. The total concentrations of the extractable fatty acids were quantified from a Podzol Bh horizon (26.2 μg g^—1), Phaeozem Ap unfertilized (48.1 μg g^—1), Phaeozem Ap fertilized (57.7 μg g^—1), and Gleysol Ap (66.7 μg g^—1). Our results demonstrate that the method is well suited to investigate the role of long‐chain fatty acids in humic fractions, whole soils and their particle‐size fractions and can be serve for the differentiation of plant growth and soil management.     

Distribution of Zinc Fractions in Some Major Soils of India and the Impact on Nutrition of Rice

Abstract

Speciation study of microelements in soils is useful to assess their retention and release by the soil to the plant. Laboratory and greenhouse investigations were conducted for five soils of different agro‐ecological zones (viz., Bhuna, Delhi, Cooch‐Behar, Gurgaon, and Pabra) with diverse physicochemical properties to study the distribution of zinc (Zn) among the soil fractions with respect to the availability of Zn species for uptake by rice plant. A sequential extraction procedure was used that fractionated total soil Zn into water‐soluble (WS), exchangeable (EX), specifically adsorbed (SA), acid‐soluble (AS), manganese (Mn)‐oxide‐occluded (Mn‐OX), organic‐matter‐occluded (OM), amorphous iron (Fe)‐oxide‐bound (AFe‐OX), crystalline Fe‐oxide‐bound (CFe‐OX), and residual (RES) forms. There was a wide variation in the magnitude of these fractions among the soils. The studies revealed that more than 90% of the total Zn content occurred in the relatively inactive clay lattice and other mineral‐bound form (RES) and that only a small fraction occurred in the forms of WS, EX, OM, AFe‐OX, and CFe‐OX. Rice (Oryza sativa L.) cultivars differ widely in their sensitivity to Zn deficiency. Results suggested that Zn in water‐soluble, organic complexes, exchange positions, and amorphous sesquioxides were the fractions (pools) that played a key role in the uptake of Zn by the rice varieties (viz., Pusa‐933‐87‐1‐11‐88‐1‐2‐1, Pusa‐44, Pusa‐834, Jaya, and Pusa‐677). Isotopic ally exchangeable Zn (labile Zn) was recorded higher in Typic Ustrochrept of Pabra soil, and uptake of Zn by rice cultivars was also higher in this soil. The kinetic parameters such as maximum influx at high concentrations (I_max) and nutrient concentration in solution where influx is one half of I_max (K_m) behaved differentially with respect to varieties. The highest I_max value recorded was 9.2×10^?7 µmol cm^?2 s^?1 at the 5 mg kg^?1 Zn rate for Pusa‐933‐87‐1‐11‐88‐1‐2‐1, and the same was lowest for Pusa‐44, being 4.6×10^?7 µmol cm^?2 s^?1 at the 5 mg kg^?1 Zn rate. The K_m value was highest for Pusa‐44 (2.1×10^?4µmol cm^?2 s^?1) and lowest for Pusa‐933‐87‐1‐11‐88‐1‐2‐1 (1.20×10^?4µmol cm^?2 s^?1). The availability of Zn to rice cultivars in Typic Ustrochrepts of Bhuna and Delhi soils, which are characterized by higher activation energy and entropy factor, was accompanied by breakage of bonds or by significant structural changes.     

Effect of Holding Temperature on the Structures of Mung Bean Starch Gels and Noodles

The effect of storage temperatures (‐10, +1, and +10°C) on the structural organization of mung bean starch gels and noodles was studied by acid hydrolysis, X‐ray diffractometry, and gel‐permeation chromatography. The gels showed higher susceptibility to acid compared with the noodles as shown by the rate constants of the first stage of hydrolysis (k = 5.37–12.17 × 10^‐2/day and k = 4.19–4.61 × 10^‐2/day for gels and noodles, respectively). Acid hydrolysis showed no difference in the amount of resistant residues of both gels (42–46%) and noodles (44–45%), except for gels (38%) stored at ‐10°C. The acid‐resistant residues of both the gels and noodles had a B‐type X‐ray diffraction pattern (major reflections at 2θ = 19, 24, and 25°). The acid‐resistant residues of the unstored sample and those stored at ‐10°C for both gels and noodles contained chains with DP 46–54 and after debranching yielded two peaks with DP 29–39 and DP 15–19. The acid‐resistant residues of gels and noodles stored at +1 and +10°C contained chains with DP 35–37 and after debranching showed two chain populations with DP 31–33 and DP 14–19. These results indicate the greater participation of amylopectin in the retrogradation process occurring during storage at +1 and +10°C.     

Kinetics of nonexchangeable‐potassium release and plant response in some calcareous soils

Nonexchangeable K⁺ constitutes a slowly available reserve that may significantly influence K⁺ fertility of soils. Laboratory and greenhouse experiments were conducted to characterize the K⁺ supply and nonexchangeable K⁺–release kinetics in 10 calcareous soils using 0.01 M CaCl₂ and 0.01 M oxalic acid extractions. Total K⁺ uptake by wheat (Triticum aestivum L.) grown in the greenhouse was used to measure plant‐available K⁺. The release of K⁺ was characterized by an initial fast rate followed by a slower rate. The nonlinear relationship in the early stages of the K⁺ release may be attributed to the edge sites, and release of K⁺ from interlayer exchange sites may be responsible for the second part of the K⁺ release. Kinetics of K⁺ release was described best with power function, which showed the best fit of the four models tested. Parameters of kinetics models in 0.01 M CaCl₂ were significantly related to K⁺ uptake by wheat. Potassium release was also correlated to initial NH₄OAc‐extratable K⁺ and to HNO₃‐extractable K⁺.     

Sorption behavior of selenium and antimony in soils as a function of phosphate ion concentration

Abstract

Both selenium (Se) and antimony (Sb) are major soil and water pollutants. Their sorption behavior in a soil–plant system was studied. Soil–soil solution distribution coefficients (K _ds) for Se and Sb were measured, using a radiotracer, as an indicator of their sorption levels. Both Se and Sb behave as oxoanions (SeO^2? ₄, H₂PO^? ₄ and SO^2? ₄) in soil; thus, the effects of concentrations of two major oxoanions (SeO^2? ₄ and SeO^2? ₃) on Se and Sb sorption were also examined. The K _d values for Se for Japanese soils significantly correlated with the K _d values for Sb (n = 141). The K _ds of both Se and Sb similarly decreased with increasing SbO^? ₃ concentration. These results indicated that the sorption of Se and Sb was similarly controlled by a ligand-exchange mechanism such as phosphate sorption in soil. However, an increase in the concentration of SeO^2? ₃ did not decrease the K _ds of Se and Sb. Furthermore, the ligand-exchangeable fractions of stable Se and Sb in major Japanese soils were determined by extraction with 0.1 mol L^?1 Na₂HPO₄ solution. For both Se and Sb, the phosphate-extractable fractions were 10-fold higher for Se and fivefold higher for Sb than their water-soluble fractions. Although the total Se and Sb amounts in soils were the same, their ligand-exchangeable fractions were different. Approximately 0.9–12% of total Se and 0.2–1.3% of total Sb were extracted by the phosphate solution. These findings suggested that Se was more likely to be mobilized by the addition of phosphate than Sb. The effect of plant-available phosphate in the soil and the phosphate sorption capacity of soil on Se and Sb availabilities for plants were also examined using a pot experiment with soybean plants. The experimental results suggested that a high content of available phosphate and/or low phosphate sorption capacity of soil increased both Se and Sb availabilities to the plant. However, the results also suggested that the soil Se availability to the plant was higher than that of Sb even though the soil total Se and Sb amounts were the same.     

Oxygen Transfer and Industrial Wastewater Treatment Efficiency of a Vertically Moving Biofilm System

A vertically moving biofilm system (VMBS) was developed to treat wastewater. In this system, the biofilm grows on a biofilm module consisting of plastic media that is vertically and repeatedly moved up into the air and down into the water. The objectives of this study were to investigate the oxygen transfer efficiency and industrial wastewater treatment performance of the VMBS. The oxygen transfer coefficient (K _L a) depended on the movement frequency (n) of the biofilm module and was proportional to n ^1.67. K _L a values measured were within the range of 0.0001 to 0.0027 s^-1. The VMBS exhibited good carbonaceous removal when treating industrial wastewater produced in a factory manufacturing synthetic fibres. Removal efficiency of filtered chemical oxygen demand (COD) and biological oxygen demand (BOD₅) was up to 93.2 and 97.9%, respectively. The volumetric removal rates of filtered COD and BOD₅ reached 1320 g COD m^-3 day^-1 and 700 g BOD₅ m^-3 day^-1. The areal organic removal rates, based on the surface area of the biofilm substrata, were 16 g BOD₅ m^-2 day^-1 and 39 g COD m^-2 day^-1. No clogging occurred during the experiment. The mean areal biofilm mass increased with increasing the mean areal BOD₅ removal rate. The new biofilm process has such advantages as high carbonaceous oxidation, energy saving, simpleconstruction and easy operation for industrial wastewater treatment.     

Turbulent mixing accelerates PAH desorption due to fragmentation of sediment particle aggregates

Purpose

Stripping contaminants from sediments with granular activated carbon (GAC) is a promising remediation technique in which the effectiveness depends on the rate of contaminant extraction from the sediment by the GAC. The purpose of the present study was to investigate the effect of mixing intensity on the short-term extraction rate of polycyclic aromatic hydrocarbons (PAHs) from contaminated sediment.

Materials and methods

PAH desorption from sediment at a wide range of rotational speeds (min^?1; rotations per minute (rpm)) was monitored by uptake in Tenax polymeric resins using a completely mixed batch reactor. Desorption data were interpreted using a radial diffusion model. Desorption parameters obtained with the radial diffusion model were correlated with particle size measurements and interpreted mechanistically.

Results and discussion

Fast desorption rate constants, D _e /r ², with D _e the effective diffusion coefficient and r the particle radius, ranged from 3.7 × 10^?3 to 1.1 × 10^?1 day^?1 (PHE) and 6 × 10^?6 to 1.9 × 10^?4 day^?1 (CHR), respectively, and increased with the intensity of mixing. The D _e /r ² values would correspond to D _e ranges of 1.8 × 10^?14–1.2 × 10^?16 m² × day^?1 and 1.8 × 10^?12–3.7 × 10^?15 m² × day^?1, assuming fast desorption from the measured smallest particle size (9 μm) classes at 200 and 600 rpm, respectively.

Conclusions

Desorption of PAHs was significantly accelerated by a reduction of particle aggregate size caused by shear forces that were induced by mixing. The effective intra-particle diffusion coefficients, D _e , were larger at higher mixing rates.

     

Effect of flow rate on the adsorption and desorption of glyphosate,simazine and atrazine in columns of sandy soils

Adsorption and desorption of the herbicides glyphosate [N-phosphonomethyl-aminoaceticacid], simazine [6-chloro-N,N′-diethyl-1,3,5-triazine-2,4-diamine] and atrazine [6-chloro-N²-ethyl-N⁴-isopropyl-1,3,5-triazine-2,4-diamine] were studied in four sandy soils from Western Australia. Distribution coefficients (K_ds) were calculated from breakthrough curves (BTCs) resulting from leaching step changes in concentrations through small saturated columns of soil at flow rates ranging from 0.3 to 30 m day^–1. A comparison was made with K_ds obtained after batch equilibrating solutions of the herbicides with the same soils. The K_ds of herbicides in soils decreased with increasing flow rate and most strongly for glyphosate in soils rich in clay content. Resulting increases in mobility of about 40–50% were estimated for simazine and atrazine and > 50% for glyphosate at flow rates of 3 m day^–1. Adsorption and desorption rates were estimated by fitting numerically simulated BTCs to experimental BTCs. Best fits were obtained with a time-dependent Freundlich adsorption equation. The resulting coefficient for time dependency in the equation suggests that the rates of adsorption and desorption are controlled mainly by diffusion in an adsorbing layer on or in soil particles.     

Effect of soil amendments on fractionation of Selenium‐enriched soil

Abstract

This study was to determine the effect of soil amendments on the fractionation of selenium (Se) using incubation experiments under simulated upland and flooded conditions. The treatments were as follows: 1) control [soil + sodium selenite (Na₂SeO₃) (1 mg Se kg^‐1)]; 2) control + calcium carbonate (CaCO₃) (5 g kg^‐1); 3) control + alfalfa (40 g kg^‐1); and 4) control + CaCO₃ (5 g kg^‐1) + alfalfa (40 g kg^‐1). After a 90‐day incubation, soil was sampled and fractionated into five fractions: 1) potassium sulfate (K₂SO₄)‐soluble fraction (available to plants); 2) potassium dihydrogen phosphate (KH₂PO₄)‐exchangeable fraction (potentially available); 3) ammonium hydroxide (NH₃H₂O)‐soluble fraction (potentially available); 4) hydrochloric acid (HCl)‐extractable fraction (unavailable); and 5) residual fraction (unavailable). Compared with the control, CaCO₃ increased the K₂SO₄ fraction at the expense of the NH₃H₂O fraction. Alfalfa increased both the K₂SO₄ and residual fractions but reduced the KH₂PO₄ and NH₃H₂O fractions. The CaCO₃‐alfalfa treatment had a similar effect to the alfalfa treatment alone. The comparison between the upland and flooded conditions showed that the flooded condition generally increased the residual fraction and decreased the potentially‐available fractions. In general, CaCO₃ was a better amendment because it not only increased the available fraction but also maintained the potentially available fractions at a high level. The application of Na₂SeO₃ and use of appropriate soil amendments can improve Se availability in soil.     

Effect of long‐term swine‐manure application on soil hydraulic properties and heavy metal behaviour

This study evaluated the effect of 13 years of swine‐manure application on the changes in soil hydraulic properties, and as associated physicochemical properties, with a focus on heavy metal mobility. Various soil hydraulic properties were measured, including soil water retention (SWR), saturated field hydraulic conductivity (K_fs) and unsaturated field hydraulic conductivity (K_funsat) using a disc infiltrometer. Heavy metal mobility was evaluated with a sequential extraction procedure. At 0–30 cm soil depth in the heavily manured plot (SMhigh plot), SWR at 0 to ?100 kPa was significantly larger than in plots amended with a standard amount of manure (SMstd plot) or with chemical fertilizer (CF plot). K_fs and K_funsat values in both manure‐amended plots were less than in the CF plot under dry soil conditions but greater than those of the CF plot under wet soil conditions. Furthermore, K_fs and K_funsat did not necessarily increase with manure application rates. On the other hand, high‐mobility metal fractions, such as the exchangeable fraction of Zn, and the CH₃CO₂Na‐extractable fraction of Zn and Mn, and the metal–organic complex fractions of Zn, Cu and Mn, increased with the greater manure application rate. In addition, low‐mobility metal fractions, the organically bound fractions of Zn, Cu and Mn in the high SM plot and the easily reducible metal oxide fraction of Mn in both manure‐amended plots were probably affected and released into high‐mobility fractions. This indicated that manure application changed the soil redox conditions by improving the soil structure, depending on the water content of soil pores. Despite the reduction of K_fs and K_funsat by heavy manure application, the transport of high‐mobility metal fractions with either surface water flow or infiltration water flow could be controlled by soil water content at the beginning of a rain or irrigation event.     

低温冷害下不同播期和播量对冬小麦籽粒灌浆特征的影响

为解析低温冷害下不同播期和播量对小麦籽粒灌浆特征的影响,选择‘济麦22’和‘皖麦52’为试验材料,在安徽省蒙城县和太和县同步开展不同播期[早播(10月3日)和适播(10月15日)]和播量[N1(6×104株·666.7m?2)、N2(10×104株·666.7m?2)、N3(14×104株·666.7m?2)和N4(18×104株·666.7m?2)]互作试验。田间冷害和籽粒灌浆过程的调查结果表明,‘济麦22’和‘皖麦52’早播时冷害致灾严重,‘济麦22’抗寒性强于‘皖麦52’;同一播期下,2个品种单粒重变化趋势基本一致,‘济麦22’相应处理单粒重均高于‘皖麦52’,同一品种随播量增加单粒重呈降低趋势。利用Matlab编程获取小麦籽粒Richards方程的灌浆次级参数,不同播期之间各参数存在一定规律性,其中,起始势(R0)、平均灌浆速率(Vmean)、中期灌浆时间(T2)、前期籽粒灌浆速率(Vp1)和中期灌浆速率(Vp2)以适播处理较高,前期灌浆时间(T1)、后期灌浆时间(T3)和后期灌浆速率(Vp3)以早播处理较高,即早播小麦受低温冷害致灾严重。相同播期条件下,2个品种随播量变化趋势基本一致,随播量增加T1和Vp3逐渐增加,R0、Vmean、T2、T3、Vp1、Vp2和最终干重(Wmax)则呈降低趋势;品种间表现为‘济麦22’的Vmean、T2、T3和Vp1较高,‘皖麦52’的R0、T1、Vp2和Vp3较高。关联性分析结果表明:早播条件下,与单粒重关联性较高的参数有T2(0.871 1)、T3(0.809 6)、Vmean(0.777 5)和Vp2(0.761 6);适播条件下,与单粒重关联性较高的参数有T2(0.906 1)、R0(0.873 8)、Vmean(0.837 2)和Vp2(0.805 6)。通径分析结果表明:春季低温冷害发生时,无论在早播还是适播,起始势对单粒重均具有积极的正效应;灌浆中后期时间的延长有利于单粒重的增加,而灌浆前期时间的增加则具有负效应;前期和中期籽粒灌浆速率的提高有利于单粒重的增加,后期籽粒灌浆速率则具有负效应。因此,提高灌浆起始势和延长中后期灌浆时间对增加籽粒干重具有重要作用。     

Pulsed Nuclear Magnetic Resonance (PNMR) Study of Rice Starch Retrogradation

Although pulsed NMR (PNMR) has been used for qualitative study of starch retrogradation in selected systems, validation is necessary for its application to new systems. PNMR was used to analyze the retrogradation of rice starches in purified form, in rice flour, and in cooked rice grains. The standard curves between the relative solid content (S′, %) by PNMR and the percentage of gelatinized starch (GS, %) were determined for common rice flour, common rice starch, and waxy rice starch at different moisture contents. The coefficients of linear regression for these curves (R²) were all >0.997. Starches with different amylose contents were tested for S′ values at the stages of freshly gelatinized, retrograded (4°C, 18 days), and reheated (90°C, 20 min). The S′ of reheated starch (S′_reheat) was similar to the S′ of freshly gelatinized starch (S′₀), so we concluded that the increase in S′ during storage corresponded to amylopectin retrogradation. The effect of moisture content on retrogradation of rice starch, rice flour, and cooked rice grains was studied by PNMR, and the data were interpreted using the Avami equation. Decreasing the moisture content increased the rate of retrogradation and led to a higher parameter k and a lower parameter n. For moisture content in the range studied, PNMR can be used to follow amylopectin retrogradation of different rice starch systems.