Matrix-Based Fertilizers Reduce Nutrient Leaching While Maintaining Kentucky Bluegrass Growth

We tested the efficacy of matrix-based fertilizers (MBFs) to improve Kentucky bluegrass (Poa pratensis L.) growth while reducing NH, NO₃, dissolved reactive phosphorus (DRP), and total phosphorus (TP) compared to commercial slow-release fertilizer (SRF) Polyon®, ESN®, and Avail® in greenhouse column studies. The MBFs covered a range of inorganic N and P in compounds that are relatively loosely bound (MBF6) and more tightly bound compounds (MBF7) with Al(SO₄)₃18H₂O and/or Fe₂(SO₄)₃3H₂O and with high ionic exchange compounds starch, cellulose, and lignin. The total amount of NO₃ and NH₄ leached was greater from columns receiving Polyon® and ESN® fertilizers than all other treatments. The MBF6+Avail® or MBF7+Avail® fertilizers leached 64–68% less NO₃ than Polyon® (43-0-0) and ESN® (46-0-0), and 73–76% less TDP and TP than Avail® (10-34-0). A greater amount of NO₃ was leached from the MBF6+Avail® and the MBF7+Avail® treatments than the other MBF fertilizer treatments. Shoot and root biomass were greater when plants received the Avail®, MBF6+Avail®, and MBF7+Avail® fertilizer treatments than the other fertilizer treatments. When combined with small quantities of commercial SRFs, these new MBFs were able to maintain plant growth while reducing N and P leaching. These new MBF formulations do not depend on organic or inorganic coatings to reduce N and P leaching and with further testing and development could be effective commercial fertilizers.     

Matrix Based Fertilizers Reduce Nitrogen and Phosphorus Leaching in Greenhouse Column Studies

We tested the efficacy of matrix based fertilizer formulations (MBF) that reduce NH₄, total phosphorus (TP), total reactive phosphorus (TRP) and dissolved reactive phosphorus (DRP) in leachate. The MBF formulations cover a range of inorganic N and P in compounds that are relatively loosely bound (MBF1) to more moderately bound (MBF2) and more tightly bound compounds (MBF3) mixed with Al(SO₄)₃ H₂O and/or Fe₂(SO₄)₃ and with the high ionic exchange compounds starch, chitosan and lignin. Glomus interadicies, a species of arbuscular mycorrhizal fungal spores that will form mycorrhizae in high nutrient environments, was added to the MBF formulations to increase plant nutrient uptake. When N and P are released from the inorganic chemicals containing N and P the matrix based fertilizers likely bind these nutrients to the Al(SO₄)₃ H₂O and/or Fe₂(SO₄)₃ starch–chitosan–lignin matrix. We tested the efficacy of the MBFs to reduce N and P leaching compared to Osmocote^® 14-14-14, a slow release fertilizer (SRF) in sand filled columns in a greenhouse study. SRF with and without Al and Fe leached 78–84% more NH₄, 58–78% more TP, 20–30% more TRP and 61–77% more than MBF formulations 1, 2, and 3 in a total of 2.0 liters of leachate after 71 days. The concentration and amount of NO₃ leached among SRF and MBF formulations 1 and 2 did not differ. The SRF treatment leached 34% less NO₃, than MBF3. Total plant weight did not differ among fertilizer treatments. Arbuscular mycorrhizal infection did not differ among plants receiving SRF and MBF formulations 1, 2 and 3. Although further greenhouse and field testing are called for, results of this initial investigation warrant further investigation of MBFs.     

Redistribution of cadmium,copper, lead,nickel, and zinc among soil fractions in a contaminated calcareous soil after application of nitrogen fertilizers

This study was conducted to evaluate the redistribution of the heavy metals Cd, Cu, Pb, Ni, and Zn among different soil fractions by N fertilizers. In a lab experiment, soil columns were leached with distilled water, KNO₃, NaNO₃, NH₄NO₃, or Ca(NO₃)₂ · 4H₂O. After leaching, soil samples were sequentially extracted for exchangeable (EXCH), carbonate (CARB), organic‐matter (OM), Mn oxide (MNO), Fe oxide (FEO), and residual (RES) fractions. Distilled water significantly increased the concentrations of Cd and Ni in EXCH fraction, while concentration of Cu and Zn did not change significantly. Application of KNO₃, NaNO₃, NH₄NO₃, or Ca(NO₃)₂ · 4H₂O significantly increased the concentrations of Cd and Zn in EXCH fraction, while concentration of Pb and Ni was decreased. Application of all fertilizers caused an increase of Cu in the OM fraction. Moreover, leaching with these solutions significantly increased Cd [except in Ca(NO₃)₂ · 4H₂O], Cu, and Zn concentrations in the CARB fraction, while Pb and Ni concentrations were decreased. With application of all leaching solutions, Zn in the EXCH, CARB, FEO, and MNO fractions was significantly increased, while Zn in the OM fraction did not change. The mobility index indicated that Ca(NO₃)₂ · 4H₂O increased the mobility of Cd, Cu, and Zn in the soil, whereas NaNO₃ decreased the mobility of Pb and Ni in the soil. The mobility index of Pb decreased by all leaching solutions. Thus, these results suggest that applying N fertilizers may change heavy‐metal fractions in contaminated calcareous soil and possibly enhance metal mobility and that N‐fertilization management therefore may need modification.     

Influence of cationic impurities in acidulated phosphates on the availability of phosphorus to two corn crops

Abstract

Based on the problems that arises from the presence of cationic impurities in rock phosphates for fertilizer production, a greenhouse experiment consisting of two consecutive corn crops was conducted in order to evaluate the plant availability of phosphorus (P) in the fraction soluble only in neutral ammonium citrate (NAC) and also in the NAC+H₂O fraction of acidulated phosphate fertilizers produced from Brazilian raw materials with different amounts of cationic impurities. The experiment was conducted with samples of a Red‐Yellow Latosol (Typic Hapludox) in a completely randomized design with four replications. Four acidulated phosphates obtained by sulfuric acid (H₂SO₄) solubilization of different Brazilian raw materials were studied. Monocalcium phosphate [Ca(H₂PO₄)H₂O] (MCP) was included as a standard source of P as well as samples which were previously leached to remove the water‐soluble P, and therefore, contained essentially the NAC‐soluble fraction. The fertilizers were thoroughly mixed with the whole soil in the pots (mixed application), or with only 1% of its volume (localized application), at the rates of 50 and 100 mg P kg^‐1, based on the calculated content of P soluble in NAC+H₂O. Corn (Zea mays L.) was the test crop grown in two sequences of 35 days. After each 35‐day period, dry matter yield and P accumulated in the plant tops were determined. Results were evaluated by analysis of variance considering the factors, (i) acidulated phosphates, (ii) rate of P application, (iii) leaching, and (iv) methods of application. In a second analysis, the leached phosphates were considered as additional levels of the phosphate factor as well as for MCP. The Tukey test at the 0.05 significance level was utilized for mean separation. Results from this study clearly demonstrated that increasing the amounts of cationic impurities in the raw materials decreased the concentration of water‐soluble P and NAC+H₂O‐soluble P as well as water‐soluble P and NAC+H₂O‐soluble P ratio of the fertilizer obtained. From the results in the first corn cropping, the P in the NAC fraction for the studied Brazilian phosphate was not as available to plants as was the P in the NAC+H₂O fraction or in the pure MCP. The NAC+H₂O method was not an adequate index for evaluating the P availability of the studied sources. No interaction between P sources, leaching, and method of application was found in the second corn cropping.     

Aluminium sulphate solubility in acid forest soils in Denmark

Ion leaching in 3 sandy spruce forest soils of different origin and pH was investigated in the laboratory. Zero-tension lysimeters containing undisturbed soil columns of varying soil depth were subjected to H₂SO₄ loadings for a period of 9 weeks. The analysis of the resulting leachate supports the hypothesis that Al-sulphate minerals may form in acidic soils when exposed to acid (H₂SO₄) deposition. In the B horizon of a glaciofluvial sandy soil (pH 4.2), both H⁺ and sulphate ions were retained to maintain 2pH + PSO₄ = 11.9 in the leachate solutions. This relation between H⁺ and sulphate activity may be due to an adsorption mechanism or a precipitation mechanism. The precipitation mechanism is favored by the good fit of leachate composition to the conditions for jurbanite [AlOHSO₄] formation from gibbsite [Al(OH)₃]. In the B horizon of a sandy till at pH 3.7, the Al in soil solution (0.5 mmol L^?1) was leached with sulphate. As the sulphate load was increased, some sulphate was retained. This may also be due to the dissolution and precipitation of an Al-sulphate mineral. The ion activity products of leachate solutions from the B horizon of this soil were close to the pK_s reported for jurbanite. The conditions for the possible existence and/or formation of Al-sulphate minerals in acidic soils are discussed.     

Nitrogen uptake of sorghum (Sorghum bicolor L.) from tree mulch and mineral fertilizer under high leaching conditions estimated by nitrogen-15 enrichment

 The effects of applying either inorganic fertilizer or leaf mulch of Acacia saligna (Labill.) H.L. Wend. on yields of Sorghum bicolor (L.) were compared with an unfertilized control under the high leaching conditions of runoff irrigation in a dry tropical environment. The N use efficiency and transfer from ¹⁵N-labelled (NH₄)₂SO₄ or acacia leaves to the sorghum differed in quantity and quality. Only 6% of the applied mulch N was retrieved in the crop, in contrast to 21% of the fertilizer N. The proportions of N in the crop derived from the fertilizers were small, amounting to 7% and 28%, respectively, in the mineral fertilizer and mulch treatments. However, the application of inorganic fertilizer and mulch significantly increased crop grain yield (P<0.05 and P<0.1, respectively), biomass production and foliar N contents (P<0.05). The inorganic fertilizer improved crop yields to a larger extent than mulching. At the same time, more N was lost by applying (NH₄)₂ SO₄ than leaf mulch: only 37% of the N of applied (NH₄)₂ SO₄ was found in the crop and the soil (0–0.3 m), but 99% of the mulched N. High NO₃ ^– contents in the topsoil of the inorganic fertilized sorghum treatments indicated the risk of N leaching. However, more important may have been gaseous N losses of surface-applied NH₄ ⁺. From a nutrient conservation point of view, mulches should be given preferance to inorganic fertilizers under high soil pH and leaching conditions, but larger improvements of crop yields could be achieved with mineral fertilizers. Received: 29 July 1998     

Ability of sorption–desorption experiments to predict potassium leaching from calcareous soils

When potassium (K⁺) fertilizers are applied to the soil, K⁺ is subject to displacement through the soil profile. Leaching can play an important role in agricultural K⁺ losses that can decrease groundwater quality. To avoid overfertilization, estimation of K⁺ leaching from soil is important. The ability of the soils to retain K⁺ against leaching varies according to the adsorption coefficient of the soils. The aim of this study was to relate the K⁺ leaching from a wide range of calcareous soils to the values obtained from a sorption–desorption experiment. The soil columns were leached with 10 mM CaCl₂ solution and the leachate was analyzed for K⁺. The breakthrough curves for K⁺ were different, and the amounts of K⁺ leached varied considerably between different soils. In these calcareous soils where crops are irrigated with water containing significant concentrations of Ca²⁺ and other cations, large amounts of K⁺ will be leached. Cumulative K⁺ leached after five pore volumes leaching with 10 mM CaCl₂ was significantly (r = 0.776, p < 0.01) related to the equilibrium K⁺ concentration. The results of this study enabled us in many cases to estimate the K⁺ leaching from soil without conducting column experiments, minimizing the laborotary work.     

Auswaschung von Nährstoffen durch sauren Nebel aus jungen intakten Fichten (Picea abies)

Leaching of nutrients out of young intact spruce (Picea abies) by acid fog The effect of acid fog on the leaching of minerals and carbohydrates out of needles of five year old spruce trees (Picea abies) was studied. The fogs were prepared from H₂SO₄ and HNO₃ (2:1) with a pH of 2.75 (acid treatment) and 5 (control treatment). The acid fog leached significantly higher amounts of K, Ca, Mg, Mn, and Zn as well as carbohydrates as compared with the control fog. The absolute quantities of minerals leached, however, were low and amounted to only some percent of the minerals generally present in needles. Except Zn, of which the quantity leached was about as high as the Zn needle content. Nevertheless the Zn concentration in the needles treated with acid fog was not lower than the Zn concentration in the control needles suggesting that the lost Zn was quickly compensated by Zn uptake. In the treatments with acid fog damage symptoms appeared at the end of the experimental period. In the older needles a weak chlorosis occurred; from the needles of the 1^st year some turned redish brown. In the acid fog treatments all needles lacked brightness while the control needles looked bright. These symptoms were similar to those under field conditions of older spruce trees with the ?lametta syndrom”?. Electron microscopic investigation revealed that the wax layer of the needles treated with acid fog was badly damaged.     

Phosphorus bioavailability of sewage sludge‐based recycled fertilizers

Six phosphorus (P) fertilizers recycled from sewage sludge [Struvite SSL, Struvite AirPrex®, P‐RoC®, Mephrec®, Pyrolysis coal and Ash (Mg‐SSA)] were tested for their plant availability in potted soil of pH 7.2 under greenhouse conditions. The crop sequence simulated a rotation of red clover (Trifolium pratense L.), maize (Zea maize L.), and ryegrass (Lolium perenne L.). Other P fertilizer treatments included: Phosphate Rock (PR), Calcium dihydrogen phosphate [Ca(H₂PO₄)₂], and an unfertilized control. Additionally, soil was regularly inoculated with two strains of plant growth‐promoting rhizobacteria (PGPR; Pseudomonas sp. Proradix, and Bacillus amyloliquefaciens) to test their ability to increase P availability to plants. Sequential P fractionation was conducted to link the amount of readily available P in fertilizers to plant P acquisition. Shoot P content and dry matter of maize decreased in the following order: Struvite SSL ≥ Ca(H₂PO₄)₂ > P‐RoC® ≥ Struvite AirPrex® ≥ Mephrec® > Pyrolysis coal ≥ Mg‐SSA ≥ PR ≥ unfertilized. Rhizobacteria did not affect shoot biomass or P content. The results show that red clover might have mobilized substantial amounts of P. Sequential P fractionation was not suitable to predict the efficacy of the fertilizers. Generally, the sewage sludge‐based fertilizers tested proved to be suitable alternative P sources relevant to organic farming systems. However, the efficacy of recycled fertilizers is strongly dependent on their specific production conditions.     

Nitrogen Recovery and Transformation from a Surface or Sub-Surface Application of Controlled-Release Fertilizer on a Sandy Soil

ABSTRACT

Controlled-release fertilizers (CRF) are used to reduce leaching of nutrients, especially nitrate-nitrogen (NO₃ ^?-N) to groundwater, caused mainly by application of soluble N fertilizers to sandy soils in Florida. A leaching column study was conducted to evaluate N release and transformation from a CRF (CitriBlen) over a 16-week period when it was applied on the soil surface or incorporated into the soil. When one pore volume of water was applied to column weekly or biweekly, the CRF released urea-N slowly over time with three peaks of release on 3–4, 8, and 12 week after application. Both ammonium-nitrogen (NH₄ ⁺-N) and NO₃ ^?-N were leached in large amounts on week 2, likely from soluble forms of N. Cumulatively, the most leached N at the end of study was in the NH₄ ⁺ form, followed by the NO₃ ^? form. The sum of all N forms leached and volatilized accounted for 53–69% of total N applied. Total N recovery was 70% and 93% of total N applied for surface and sub-surface application of the fertilizer, respectively. It was indicated that the better recovery rate found with sub-surface application may have been due to minimized N loss by volatilization. Sub-surface application of fertilizer resulted in more than three times NH₄ ⁺-N remained in soil, compared with surface application. On average for both application treatments throughout 16-week period, 5.8 h was required for ammonification and 4.7 d for nitrification to occur after N release from the fertilizer. Characterization of CRFs for specific soil type, leaching volume and cycle, and application manner as well as knowledge of N requirement of the crop will allow for the Best Management Practices of these fertilizers, thus obtaining optimum yields and minimizing nutrient losses from CRFs.     

Using Organic Matter with Chemical Amendments to Improve Calcareous Sodic Soil

Abstract

Kangping soil in northeast China is a sodic soil characterized by a high pH and excessive sodium. The high pH and excessive sodium in sodic soils generally cause loss of soil structure, reduce hydraulic conductivity (HC), increase soil hardness, and make the soil unproductive land. After we mixed organic matter (rice straw) and chemical amendments (H₂SO₄, CaSO₄, and FeSO₄), a column experiment was conducted to evaluate the physical and chemical properties of the soil influenced by the changes in HC, penetrability of soil s`urface, pH, electrical conductivity, CO₃ ^2‐, HCO₃ ^?, Ca²⁺, Na⁺, sodium adsorption rate (SAR), available phosphorus (P) and iron (Fe), and leached P.

Organic matter decreased the concentrations of CO₃ ^2‐, HCO₃ ^?, and Na⁺ in soil solution and increased the total volume of the leachate. Organic matter also reduced the amount of available Fe and increased the available P. However, organic matter did not affect the penetrability of the soil surface as much as soil hardness, HC, and SAR within the short period of this experiment. Among the chemical amendments, H₂SO₄ and FeSO₄ were more effective than CaSO₄ to restore HC, electrical conductivity, Na⁺, and SAR. The chemical amendments, compared with organic matter, significantly leached P from the soil in this study, but the leaching was independent of the concentration of available P in the soil. The CaSO₄ had the strongest effect in increasing leached P from the soil without changing the concentration of available P in the soil. Organic matter with added CaSO₄ leached P from the soil more than all other treatments.     

Sulphate Adsorption in Soils of North and Northeast Iran

Abstract

Gypsum (CaSO₄ · 2H₂O) is used in agriculture both as a source of calcium (Ca) and sulphate (SO₄ ^2?) and as an amendment to improve soil structure. The effect of gypsum on the adsorption of SO₄ ^2? in irrigated and nonirrigated soils was examined. Almost all of the indigenous sulphate (SO₄) in a range of Golesthan and North Khorasan soils with moderate pH values (>6) was found to be present in the soil solution and, as a consequence, was highly susceptible to leaching. The adsorption of sulphate to the soils receiving no gypsum was greater with correlation coefficient of r=0.91 at 0 kg S ha^?1 as compared to the soils received 40 kg ha^?1 of gypsum as fertilizer with the value of r=0.88 in Golesthan Province. The same trend was observed in Khorasan Province with r=0.79 and r=0.75 with soils receiving 0 and 40 kg S ha^?1, respectively. The results were more pronounced in irrigated fields for both provinces. The amount of sulphate adsorption in Golesthan Province soils was comparatively greater than soils of Khorasan Province. The results raise questions regarding the efficiency of SO⁴‐containing fertilizers in correcting and preventing S deficiency in situations where leaching is a concern.     

Impact of tillage on microbial activity and the fate of pesticides in the upper soil

The impact of two tillage systems, plow tillage (PT) and no-tillage (NT), on microbial activity and the fate of pesticides in the 0–5 cm soil layer were studied. The insecticides carbofuran and diazinon, and the herbicides atrazine and metolachlor were used in the study, which included the incubation and leaching of pesticides from untreated soils and soils in which microorganisms had been inhibited. The mineralization of ring¹⁴C labeled pesticides was studied. The study differentiated between biotic and abiotic processes that determine the fate of pesticides in the soil. Higher leaching rates of pesticides from PT soils are explaned by the relative importance of each of these processes. In NT soils, higher microbial populations and activity were associated with higher mineralization rates of atrazine, diazinon and carbofuran. Enhanced transformation rates played an important role in minimizing the leaching of metolachlor and carbofuran from NT soils. The role of abiotic adsorption/retention was important in minimizing the leaching of metolachlor, carbofuran and atrazine from NT soils. The role of fungi and bacteria in the biodegradation process was studied by selective inhibition techniques. Synergistic effects between fungi and bacteria in the degradation of atrazine and diazinon were observed. Carbofuran was also degraded in the soils where fungi were selectively inhibited. Possible mechanisms for enhanced biodegradation and decreased mobility of these pesticides in the upper layer of NT soils are discussed.     

Canopy leaching of cations in Central European forest ecosystems – a regional assessment

The leaching of Ca, Mg, and K from canopies is a major pathway of these cations into forest soils. Our aim was to quantify rates of canopy leaching and to identify driving factors at the regional scale using annual fluxes of bulk precipitation and throughfall from 37 coniferous and deciduous forests of North and Central Europe. Total deposition of Ca, Mg, K, and H⁺ was estimated with Na as an index cation. The median canopy leaching increased in the order: Mg (0.11 kmol_c ha^–1 a^–1) < Ca (0.31 kmol_c ha^–1 a^–1) < K (0.39 kmol_c ha^–1 a^–1). Canopy leaching of Ca and K was positively correlated with the calculated total H⁺ deposition and H⁺ buffered in the canopy, whereas canopy leaching of Mg was not. With contrasting effects, fluxes of SO₄‐S and NH₄‐N in throughfall explained to 64 % (P<0.001) of the Ca canopy leaching. Fluxes of NH₄‐N and Ca were negatively correlated, suggesting that buffering of H⁺ by NH₃ deposition reduced canopy leaching of Ca. Amount of bulk precipitation and SO₄‐S in throughfall were identified as much weaker driving factors for canopy leaching of K (r²=0.28, P<0.01). Our results show that Ca is the dominant cation in buffering the H⁺ input in the canopy. At the regional and annual scale, canopy leaching of Mg appears to be unaffected by H⁺ deposition and H⁺ buffering in the canopy.     

SO42-和Cl-对稻田土壤养分及其吸附解吸特性的影响

利用长期定位试验 ,比较了长期施用含SO₄^2-和Cl^- 化肥 22年后稻田土壤的 pH值、养分状况及其吸附解吸特性。结果表明 ,长期施用含SO₄^2-化肥 ,土壤有机质、速效氮和速效钾的含量较高 ,但全量氮磷钾的含量较低 ;长期施用含Cl^- 化肥 ,土壤全量氮磷钾和速效磷的含量较高 ,但pH值相对较低。长期施用含上述二种阴离子的化肥后 ,土壤对H₂PO₄^-的最大吸附量均较大 ,且在Cl^- 处理下土壤对H₂PO₄^-吸附的结合能较大 ,而SO₄^2-处理下土壤在同等吸附量时对H₂PO₄^-的解吸量相应较多。长期施用含SO₄^2-的化肥亦使土壤对钾素的供应强度较大 (ΔK0的绝对值较大 )、缓冲能力增强 (AR0值较高 ) ,而长期施用含Cl^- 的化肥时则与SO₄^2-相反     

Magnesium-fortified phosphate fertilizers improve nutrient uptake and plant growth without reducing phosphorus availability

Magnesium (Mg) deficiency can significantly limit crop yield and quality. Separate application of straight Mg fertilizer is unattractive because of additional labor costs. Meanwhile, bulk blending Mg with other macronutrient fertilizers is also a suboptimal solution because bulk blended fertilizers often yield poor nutrient distributions. One rapid and economical alternative to alleviating Mg deficiency is to co-granulate macronutrient fertilizers with Mg. However, few commercial products have implemented this approach. One of the barriers hindering the production of Mg-fortified phosphorus (P) fertilizers is the assumption that precipitation of P with Mg will reduce P solubility. In this study, four Mg compounds, anhydrous magnesium sulfate (MgSO₄), magnesium oxide (MgO), anhydrous magnesium chloride (MgCl₂), and dolomite (CaMg(CO₃)₂), were co-granulated with mono-ammonium phosphate (MAP), and their granule strength, Mg and P availabilities, and agronomic effectiveness were evaluated. Results showed that there were no significant differences in P solubility between Mg-fortified MAP and MAP treatments. X-ray diffraction (XRD) indicated that the Mg species after co-granulation were boussingaultite (Mg(NH₄)₂(SO₄)₂·6H₂O), schertelite (Mg(NH₄)₂H₂(PO₄)₂·4H₂O), magnesium hydrogen phosphate (Mg(H₂PO₄)₂), and dolomite (CaMg(CO₃)₂). A pot experiment using an acidic soil demonstrated an average 9.6-fold increase in shoot Mg uptake, 3.0-fold increase in shoot P uptake, and 3.2-fold increase in soybean shoot dry matter in Mg-fortified MAP treatments, compared to those in MAP treatment. The current study provides a simple, effective, and low-cost approach for the addition of Mg to macronutrient fertilizers, to minimize Mg deficiency.     

Comparison of potential potassium leaching associated with organic and inorganic potassium sources in different arable soils in China

Potassium (K) leaching is detrimental to the maintenance of sustainable arable soil K fertility,especially in low-K fixation soils.It is not known whether the application of inorganic fertilizers with lower K mobility or crop straw can reduce potential K leaching in low-K fixation arable soils.The potential K leaching of 14 representative arable soils with different K fixation capacities in China was evaluated with or without the addition of K under two rainfall intensities (90 and 225 mm),and then potential K leaching was assessed in relation to five K sources (KCl,K₂SO₄,KH₂PO₄,maize (Zea mays L.) straw,and rice (Oryza sativa L.) straw).Without K addition,K leaching mainly occurred in sandy soils at 90 mm of rainfall and in soils with greater organic matter at225 mm of rainfall.With K addition,the leaching percentage of exogenous K ranged from 0.6%to 11.6%at 90 mm of rainfall and 1.2%to 21.2%at 225 mm of rainfall.The greatest K leaching occurred in soils with fewer K-bearing minerals and lower pH at both rainfall intensities.In most cases,KH₂PO₄,which has lower K mobility,markedly reduced K leaching in both high-and low-K leaching soils at the two rainfall intensities.Maize and rice straw reduced K leaching only in soils with high K leaching,regardless of rainfall amount,whereas more K was leached in soils with lower K leaching at high rainfall intensity.In conclusion,KH₂PO₄ and straw should be preferred for reducing K leaching in low-K fixation arable soils.     

Soil response to s and n treatments in a Northern New England low elevation coniferous forest

A field experiment was designed to evaluate the effects of differing forms of acidifying S and N compounds on the chemistry of soils and soil solutions in a low elevation coniferous forest in northern New England. Treatments consisted of O, 1500, 3000, and 6000 eq of SO₄ ^2? or NO₃ ^? ha^?1 for the 1987 growing season applied biweekly as H₂SO₄ or HNO₃, or in a single application as dry] (NH₄)₂SO₄. Acidifying treatments resulted in a significant increase in soil solution SO₄ ^2? (1.2 to 2.6) or NO₃ ^? (12 to 80) in the upper B horizon. Excess strong acid anion leaching was associated with an accelerated loss of base cations, particularly MG²⁺ As solutions passed through the upper 25 cm of the soil profile, mean SO₄ ^2? concentrations decreased by 5 to 50% of the initial values, indicating that much of the applied SO₄ ^2? was immobilized in the upper portion of the pedon. Elevated concentrations of adsorbed and water-soluble SO₄ ^2? indicate that abiotic adsorption of SO₄ ^2? by soils is the dominant mechanism for the initial attenuation of SO₄ ^2? concentrations in these solutions. Other soil properties showed only small or no change due to treatments over the single growing season of this study. These results indicate that H₂SO₄, HNO₃, and (NH₄)₂SO₄ can all effectively increase strong acid anion concentrations in the soil-soil solution system.     

Comparison of Analytical Methods for Quantifying the Levels of Lead,Cadmium, Chromium,and Nickel in Mineral Fertilizers and Industrial By-products

The control of contaminants in fertilizers and industrial by-products is fundamental to safe food production, and it requires low-cost, reliable test methods. The aim of this study was to evaluate the performance of the USEPA 3051a and alternative analytical methods [concentrated hydrochloric acid (HCl), 10 percent HCl, 10 percent sulfuric acid (H₂SO₄), and 50 mmol L^?1 diethylenetriaminepentaacetic acid (DTPA)] for quantifying the levels of lead, cadmium, chromium, and nickel in zinc and/or copper sources. The sample digestions with concentrated HCl, H₂SO₄, and nitric acid (HNO₃) (USEPA 3051a) were heated. Extraction without heating and stirring was employed in 10 percent HCl and 50 mmol L^?1 DTPA methods. The Graybill’s modified F-test, t-test for mean error, and the linear correlation coefficient analysis were used to compare test method performance. Equivalent results to USEPA 3051a were found with the following methods: DTPA for the extraction of lead in zinc sources and concentrated HCl and H₂SO₄ for the extraction of cadmium and chromium in copper sources. However, the absolute values of cadmium, chromium, and nickel recovered by the use of H₂SO₄ were greater regardless of the source. The greater extraction of contaminants in the evaluated methods suggests that there is need to review the official method if the aim is to quantify the total levels of these elements in raw materials and mineral fertilizers.     

氮肥品种和用量对水稻产量和镉吸收的影响研究

采用盆栽试验,研究了Cd污染土壤上,不同氮肥品种和用量对水稻产量和Cd吸收的影响。结果表明,与磷钾配施的4个氮肥处理中,施用尿素处理水稻产量最高,其次为施(NH4)2SO4和NH4Cl处理,施NH4NO3处理水稻产量最低。与施(NH4)2SO4、NH4NO3和尿素处理相比,施NH4Cl处理可显著增加水稻对Cd的吸收,并促进Cd由秸秆向籽粒的转移;而其他3种氮肥对水稻秸秆和籽粒中Cd含量的影响效应相当。适量尿素[0.2g(N)·kg-1]处理能显著降低水稻籽粒Cd含量,而不施尿素和高量尿素处理都显著提高了水稻籽粒中的Cd含量。研究表明,在Cd污染的水稻土上,采用抗Cd污染的水稻品种和优化肥、水管理措施,可使稻米中Cd含量低于国家无公害大米的限量指标。