A rapid method for estimating labile carbon and nitrogen pools in Mollisols under no-tillage

The objective of this study was to adapt the partial chemical digestion method for estimation of labile soil organic matter pools by evaluating the effect of different digestion times in Mollisols of the Argentine Pampas. The soils were sampled from nine agricultural fields under no-tillage at the 0–20 cm depth. A chemical method was performed through partial soil digestion with dilute sulphuric acid at 100°C on the basis of four digestion times: 1 (N_d1), 2 (N_d2), 4 (N_d4) and 6 (N_d6) hours. Soil organic carbon (C) and nitrogen (N) fractions were determined. The extracted organic N (N_d) ranged from 0.076 g kg^?1 to 0.273 g kg^?1, with a mean of 0.154 g kg^?1. Statistically, the means for each digestion time indicated highly significant differences (P = 0.008). High correlations were found between N_d for different times and labile C and N fractions. However, the best fit prediction was observed between N_d2 and soil total carbohydrates (CHt), with a high coefficient of determination (R² = 0.94). Partial chemical digestion for 2 h can be used as a rapid indicator to accurately predict CHt. Because of its speed and simplicity, this method may also be useful for rapid soil quality assessments.     

Effects of soil type and nitrate concentration on denitrification products (N2O and N2) under flooded conditions in laboratory microcosms

Abstract

Denitrification products nitrous oxide ((N₂O) and nitrogen (N₂)) were measured in three flooded soils (paddy soil from Vietnam, PV; mangrove soil from Vietnam, MV; paddy soil from Japan, PJ) with different nitrate (NO₃^–) concentrations. Closed incubation experiments were conducted in 100-mL bottles for 7 d at 25°C. Each bottle contained 2 g of air-dried soil and 25 mL solution with NO₃^– (concentration 0, 5 or 10 mg N L^?1) with or without acetylene (C₂H₂). The N₂O + N₂ emissions were estimated by the C₂H₂ inhibition method. Results showed that N₂O + N₂ emissions for 7 d were positively correlated with those of NO₃^– removal from solution with C₂H₂ (R² = 0.9872), indicating that most removed NO₃^– was transformed to N₂O and N₂ by denitrification. In PJ soil, N₂O and N₂ emissions were increased significantly (P < 0.05) by the addition of greater NO₃^– concentrations. However, N₂O and N₂ emissions from PV and MV soils were increased by the addition of 0 to 5 mg N L^?1, but not by 5 to 10 mg N L^?1. At 10 mg N L^?1, N₂ emissions for 7 d were greater in PJ soil (pH 7.0) than in PV (pH 5.8) or MV (pH 4.3) soils, while N₂O emissions were higher in PV and MV soils than in PJ soil. In MV soil, N₂O was the main product throughout the experiment. In conclusion, NO₃^– concentration and soil pH affected N₂O and N₂ emissions from three flooded soils.     

Nitrate Transformation and N2O Emission in a Typical Intensively Managed Calcareous Fluvaquent Soil: A 15-Nitrogen Tracer Incubation Study

A 56-day aerobic incubation experiment was performed with 15-nitrogen (N) tracer techniques after application of wheat straw to investigate nitrate-N (NO₃-N) immobilization in a typical intensively managed calcareous Fluvaquent soil. The dynamics of concentration and isotopic abundance of soil N pools and nitrous oxide (N₂O) emission were determined. As the amount of straw increased, the concentration and isotopic abundance of total soil organic N and newly formed labeled particulate organic matter (POM-N) increased while NO₃-N decreased. When ¹⁵NO₃-N was applied combined with a large amount of straw at 5000 mg carbon (C) kg^?1 only 1.1 ± 0.4 mg kg^?1 NO₃-N remained on day 56. The soil microbial biomass N (SMBN) concentration and newly formed labeled SMBN increased significantly (P < 0.05) with increasing amount of straw. Total N₂O-N emissions were at levels of only micrograms kg^?1 soil. The results indicate that application of straw can promote the immobilization of excessive nitrate with little emission of N₂O.     

Anaerobic ammonium oxidation and denitrification in a paddy soil as affected by temperature,pH, organic carbon,and substrates

Anaerobic ammonium oxidation (anammox process) widely occurs in paddy soil and may substantially contribute to permanent N removal; however, little is known about the factors controlling this process. Here, effects of temperature, pH, organic C, and substrates on potential rate of anammox and the relative contribution of anammox to total N₂ production in a paddy soil were investigated via slurry incubation combined with ¹⁵N tracer technique. Anammox occurred over a temperature range from 5 to 35 °C with an optimum rate at 25 °C (1.7 nmol N g^?1 h^?1) and a pH range from 4.8 to 10.1 with an optimum rate at pH 7.3 (1.7 nmol N g^?1 h^?1). The presence of glucose and acetate (5–100 mg C L^?1) significantly inhibited anammox activities and the ratio of anammox to total N₂ production. The response of potential rates of anammox to ammonium concentrations fitted well with Michaelis-Menten relationship showing a maximum rate (V_max) of 4.4 nmol N g^?1 h^?1 and an affinity constant (K_m) of 6.3 mg NH₄⁺-N L^?1. Whereas, nitrate addition (5–15 mg ¹⁵NO₃^?-N L^?1) significantly inhibited anammox activities and the ratio of anammox to total N₂ production. Our results provide useful information on factors controlling anammox process and its contribution to N loss in the paddy soil.     

Nitrogen mineralization indicators under semi-arid and semi-humid conditions: influence on wheat yield and nitrogen uptake

The objectives were i) to assess indicators for potential nitrogen (N) mineralization and ii) to analyze their relationships for predicting winter wheat (Triticum aestivum L.) growth parameters (yield and N uptake, N_up) in Mollisols of the semi-arid and semi-humid region of the Argentine Pampas. Thirty-six farmer fields were sampled at 0–20 cm. Several N mineralization indicators, wheat grain yield and N_up at physiological maturity stage were assessed. A principal component (PC) analysis was performed using correlated factors to grain yield and N_up. The cluster analysis showed two main groups: high fertility and low fertility soils. In high fertility soils, combining PCs in multiple regression models enhanced the wheat yield and N_up prediction significantly with a high R² (adj R² = 0.71–0.83). The main factors that explained the wheat parameters were associated with water availability and N mineralization indicator, but they differ according to soil fertility.

Abbreviations: N: nitrogen; SOM: soil organic matter; POM: particulate organic matter; SOC: soil organic carbon; SON: soil organic nitrogen; POM-C: particulate organic carbon; POM-N: particulate organic nitrogen; N_an: anaerobic nitrogen; N_hyd: hydrolyzable N; NO₃-N: cold nitrate; N₂₀₅: N determined by spectrometer at 205 nm; N₂₆₀: N determined by spectrometer at 260 nm; Pe: extractable P; N_up: wheat N uptake; NO₃-N: inorganic N in the form of nitrate; FR: fallow rainfalls (March-Seeding rainfall); FLR: flowering rainfalls (October-December rainfall); GFR: grain filling rainfall (November rainfall); CCR: crop growing season rainfall (June-December rainfall); PCA: principal component analysis; PC: principal component; MR: multiple regression     

FLOWER ABSCISSION IN PEPPER PLANTS GROWN UNDER DIFFERENT REGIMES OF NITROGEN FERTILIZATION AND PHOTOSYNTHETICALLY ACTIVE RADIATION

The effect of nitrogen fertilization on flower abscission in pepper was studied under different growth regimes. The pepper plants were irrigated with 4, 9, and 14 meq L^?1of nitrate (N4, N9, and N14). The plants were grown in winter under a low level (639 mol m^?2) of cumulative photosynthetically active radiation (PAR) (L_PAR), and in spring under a high level (1074 mol m^?2) of cumulative PAR (H_PAR). The number of flowers and flower abscission were higher under H_PAR than under L_PAR. Flower abscission was higher in response to treatment N4, than in response to treatments N9 and N14, while the flower number was significantly lower. Flower abscission was strongly correlated with growth-related parameters as well as with the carbon or nitrogen contents in plants. Neither the sucrose fluxes nor the amino acid fluxes through the flower pedicels were affected by nitrogen supply. The sucrose fluxes were strongly correlated with air temperature.     

Effects of soil pH and salt on N2O production in adjacent forest and grassland soils in central Alberta, Canada

Purpose

The effects of soil pH manipulation and KCl addition on N₂O production in adjacent forest and grassland soils in central Alberta were studied in a 16-day laboratory incubation experiment.

Materials and methods

The soils were subjected to four pH and two salt treatments: CK (control)—no addition of acid or alkali solution (pH 4.50 and 4.48 for the forest and grassland soils, respectively; same below); HCl—addition of HCl solution to lower soil pH (3.95 and 3.75); L-KOH and H-KOH—addition of 6 mL of 0.2 (5.36 and 5.57) and 0.4 (6.41 and 6.72)?mol?L^?1 KOH solution, respectively, to increase soil pH to two different levels. In order to differentiate between the effect of a change in pH and of changed salt concentrations on N₂O production, 6 mL of 0.2 (L-KCl) (4.56 and 4.41) or 0.4 mol?L^?1 (H-KCl) (4.59 and 4.42) KCl solutions were also applied as treatments to create two levels of salt application rates.

Results and discussion

Increasing pH promoted gross nitrification and cumulative N₂O production in both soils, particularly in the forest soil. However, cumulative N₂O production decreased in the forest soil but increased in the grassland soil when pH decreased. Cumulative N₂O production in the grassland soil was 36 times higher in the L-KCl treatment (1,442 μg?N?kg^?1) than in the CK (40 μg?N?kg^?1), whereas the H-KCl treatment reduced cumulative N₂O production. In contrast, in the forest soil, both KCl treatments reduced cumulative N₂O production.

Conclusions

(1) The most important factor to increase N₂O production in this study was increasing soil pH, suggesting that careful soil pH management could be used as a tool to control soil N₂O production; (2) salt effect was also involved in affecting N₂O production.     

Pilot-scale counter-current acid leaching process for Cu,Pb, Sb,and Zn from small-arms shooting range soil

Purpose

The main objective of this study was to evaluate the potential of a counter-current leaching process (CCLP) on 14 cycles with leachate treatment at the pilot scale for Pb, Cu, Sb, and Zn removal from the soil of a Canadian small-arms shooting range.

Materials and methods

The metal concentrations in the contaminated soil were 904?±?112 mg Cu kg^–1, 8,550?±?940 mg Pb kg^–1, 370?±?26 mg Sb kg^–1, and 169?±?14 mg Zn kg^–1. The CCLP includes three acid leaching steps (0.125 M H₂SO₄?+?4 M NaCl, pulp density (PD)?=?10 %, t?=?1 h, T?=?20 °C, total volume?=?20 L). The leachate treatment was performed using metal precipitation with a 5-M NaOH solution. The treated effluent was reused for the next metal leaching steps.

Results and discussion

The average metal removal yields were 80.9?±?2.3 % of Cu, 94.5?±?0.7 % of Pb, 51.1?±?4.8 % of Sb, and 43.9?±?3.9 % of Zn. Compared to a conventional leaching process, the CCLP allows a significant economy of water (24,500 L water per ton of soil), sulfuric acid (133 L H₂SO₄ t^–1), NaCl (6,310 kg NaCl t^–1), and NaOH (225 kg NaOH t^–1). This corresponds to 82 %, 65 %, 90 %, and 75 % of reduction, respectively. The Toxicity Characteristic Leaching Procedure test, which was applied on the remediated soil, demonstrated a large decrease of the lead availability (0.8 mg Pb L^–1) in comparison to the untreated soil (142 mg Pb L^–1). The estimated total cost of this soil remediation process is 267 US$ t^–1.

Conclusions

The CCLP process allows high removal yields for Pb and Cu and a significant reduction in water and chemical consumption. Further work should examine the extraction of Sb from small-arms shooting range.     

Nitrogen addition change soil N pools with litter removal or not in subtropical forest

ABSTRACT

There are many nitrogen (N) pools in soil, so their availability and different status can give information about bulk soil response to N deposition. However, the different size of N pools in forest soils and the relationship between them have not been well studied under N deposition when considering the role of litter. Here soil in an N-deposition experiment carried out for 5 years in a broad-leaved forest was used as an object to study the response of N pools to N deposition by stepwise extraction using water or solutions containing 0.5 M K₂SO₄, 2.5 M H₂SO₄ (LPI), or 13 M H₂SO₄ (LPII), and calculation of recalcitrant (RC) N pool. Under N control (CT), soil with the presence of litter had a higher N of 23.8–106.8% in the first four pools, but lower of 80.6% in recalcitrant N pool compared with soil with the absence of litter. In the absence of litter, N addition increased soil N in labile pool but decreased N in the RC pool compared to CT and these impacts were greater at high added N (HN) than low-added N (LN) rates. However, in the presence of litter, LN increased the amount of N in the K₂SO₄- extracted pool and HN reduced that in the water extracted pool. Additionally, LN and HN increased TN in the RC pool and HN increased the total soluble N (TSN) in the LPI and LPII pool. N changes in the water extraction pool were attributed to inorganic N, whereas they were NH₄ ⁺ and soluble organic N (SON) in the K₂SO₄-extracted, LPI, and LPII pools. In the presence of litter, HN increased the SON concentration in the K₂SO₄, LPI, and LPII extractions; thus, SON may be a potentially important N form for N availability. These results suggested that N additions improve the accumulation of N in RC pool with the presence of litter. The different effects of N additions on soil N pool or N form in each pool depend on litter present or not.     

Evaluation of available boron content using eight methods of extraction in different soils from Córdoba and sucre in Colombia

The aim was to evaluate eight methods of boron (B) extraction in different soils from Córdoba and Sucre, Colombia. 37 samples were collected at a depth of 0–20 cm and carried to Soil and Water Laboratory of University of Córdoba for its chemical characterization. The available boron was extracted with the following methods: modified hot water, calcium chloride (CaCl₂) 0.05, hydrochloric acid (HCl) 0.05, barium chloride (BaCl₂) 0.006, manitol 0.05 + CaCl₂ 0.01, Ca(H₂PO₄)₂H₂O 0.008 in mol L^?1, mehlich-1 and ammonium acetate (NH₄OAc) (1.0 mol L^?1, pH = 7.0). The major quantity of boron was extracted with mehlich-1, HCl 0.05 mol L^?1 and hot water, extracting 0.36, 0.29 and 0.26 mg kg^?1, respectively. The extracting solution that correlated with the hot water method was HCl 0.05 mol L^?1 (r = 0.81); followed by Ca(H₂PO₄)₂H₂O 0.008 mol L^?1 (r = 0.62) and mehlich-1 (r = 0.54). According to characteristic and heterogeneity of soils, we recommend HCl method to extract available boron.     

Effect of Graded Levels of Surface Crop Residue Application Under Minimum Tillage on Carbon Pools and Carbon Lability Index in Sorghum (Sorghum bicolor (L.) Moench)-Cowpea (Vigna unguiculata) System in Rainfed Alfisols

A long term experiment (2005–2012) was conducted in rainfed semi-arid tropical Alfisol at Hayathnagar Research Farm of Central Research Institute for Dryland Agriculture, Hyderabad, India. The aim of this experiment was to study the long-term impacts of graded levels of surface crop residue application on carbon (C) pools, aggregate associated C, C lability index and their relationship with crop yield. The experiment was conducted in a randomized block design (RBD) with minimum tillage (MT). Experimental treatments comprised of four levels of surface application of sorghum crop residues (@ 0, 2, 4 and 6 t ha^?1). The test crops, sorghum and cowpea, were grown in rotation yearly. Based on the pooled analysis of long term data (2005–2012), the study revealed that the surface application of sorghum residue @ 6 t ha^?1 and 4 t ha^?1 recorded 21% and 16% higher sorghum grain yields, respectively over control (no residue) whereas, the corresponding increase in the cowpea yield was 50% and 60%, respectively. Besides, the concentrations of soil organic carbon (SOC), inorganic carbon (IC), total carbon (TC), particulate organic carbon (POC) in the top surface soil (upper layer, 0–5cm depth) were found significantly higher than the sub-surface soil (lower layers, 5–15 cm depth) in all the treatments. Storage of soil C was assessed in soil aggregates fractions, and it was found that the smaller size aggregate fractions (0.053mm) contained significantly (p = 0.05) higher content of SOC compared to the large sized fractions (2 mm). The amount of very labile fraction of C extracted with 12 N H₂SO₄ was significantly higher (1.04 g kg^?1) with the application of sorghum stover @ 6t ha-¹ compared to other residue level treatments, in the 0-5 cm soil layer. The Lability Index (LI) increased with the increase in the amount of residues applied and was significantly higher in the surface soils compared to subsurface soil. The results of this study will be highly relevant and of significant value from the view point of managing SOC and its different pools in soil under abiotically stressed semiarid tropical Alfisols soils.     

酸性土壤磷分级新方法建立与生物学评价

土壤磷分级方法可用于估算土壤有效磷数量、不同土壤磷组分库数量及其对土壤有效磷的补充能力。以云南赤红壤、黄红壤及湖北棕红壤为供试材料,运用张守敬方法、蒋柏藩方法及本文提出的新方法,对三种酸性土壤和其石灰改良后的土壤磷进行分级研究,探讨石灰改良对酸性土壤磷组分数量及其生物有效性的影响。结果表明:Ca2-P、Al-P和Fe-P是酸性土壤主要的有效磷源,O-P(闭蓄态磷)也是潜在有效磷源,土壤中活性有机磷库相对比较稳定,可转化为高活性有效磷源供植物吸收利用。与两种经典磷分级方法相比,新方法将O-P划分为O-Al-P和O-Fe-P,O-Fe-P较好地反映了石灰处理与对照之间的土壤磷植物有效性差异。     

Gross nitrogen transformations and related N2O emissions in uncultivated and cultivated black soil

A better understanding of the nitrogen (N) cycle in agricultural soils is crucial for developing sustainable and environmentally friendly N fertilizer management and to propose effective nitrous oxide (N₂O) mitigation strategies. This laboratory study quantified gross nitrogen transformation rates in uncultivated and cultivated black soils in Northeast China. It also elucidated the contribution made by nitrification and denitrification to the emissions of N₂O. In the laboratory, soil samples adjusted to 60 % water holding capacity (WHC) were spiked with ¹⁵NH₄NO₃ and NH₄ ¹⁵NO₃ and incubated at 25 °C for 7 days. The size and ¹⁵N enrichment of the mineral N pools and the N₂O emission rates were determined between 0 and 7 days. The results showed that the average N₂O emission rate was 21.6 ng N₂O-N kg^?1 h^?1 in cultivated soil, significantly higher than in the uncultivated soil (11.6 ng N₂O-N kg^?1 h^?1). Denitrification was found to be responsible for 32.1 % of the N₂O emission in uncultivated soil, and the ratio increased significantly to 43.2 % in cultivated soil, due to the decrease in soil pH. Most of the increase in net N₂O-N emissions observed in the cultivated soil was resulting from the increased production of N₂O through denitrification. Gross nitrification rate was significantly higher in the cultivated soil than in the uncultivated soil, and the ratio of gross nitrification rate/ammonium immobilization rate was 6.87 in cultivated soil, much larger than the uncultivated soil, indicating that nitrification was the dominant NH₄ ⁺ consuming process in cultivated soil, and this will lead to the increased production of nitrate, whereas the increased contribution of denitrification to N₂O emission promoted the larger emission of N₂O. This double impact explains why the risk of N loss to the environment is increased by long-term cultivation and fertilization of native prairie sites, and controlling nitrification maybe effective to abate the negative environmental effects.     

Changes in Nitrogen,Phosphorus, and Potassium in a Long‐Term Continuous Maize–Wheat Cropping System in India

In a long‐term maize–wheat rotation at the Punjab Agricultural University, Ludhiana, India (subtropical climate), the effects of nitrogen (N), phosphorus (P), and potassium (K) addition on soil fertility and forms of inorganic P and K in the plow layer of an alkaline sandy loam soil were measured after 11 and 22 years of cropping. The treatments comprised four rates of N (0, 60, 120, and 180 kg N ha^?1) as urea, three rates of P (0, 17.5, and 35 kg P ha^?1) as single superphosphate, and two rates of K (0 and 33 kg K ha^?1) as muriate of potash. The treatments selected for the present study were N₀P₀K₀, N₁₂₀P₀K₀, N₁₂₀P_17.5K₀, N₁₂₀P₃₅K₀, N₁₂₀P_17.5K₃₃, and N₁₂₀P₃₅K₃₃. A significant year × treatment interaction in decreasing available N [alkaline potassium permanganate (KMnO₄)–oxidizable N) status of soils was found in all the treatments. Available P (Olsen P) in the control plot decreased over time whereas in plots with added P, available P increased significantly after years 11 and 22, with the greatest increase in the N₁₂₀P_17.5K_o treatment. Compared to the initial values, continuous P fertilization resulted in greater total P and chloride P concentrations after 11 and 22 years. Although sodium hydroxide (NaOH) P and sulfuric acid (H₂SO₄) P increased in P‐treated plots from the start of the trial to year 11, they decreased from year 11 to year 22. Among these inorganic P forms, chloride P was significantly positively correlated with P uptake (r = 0.811*). When only N and P were applied, available K [ammonium acetate (NH₄OAc)–extractable K] significantly decreased over time. In plots without K addition, water‐soluble and exchangeable K decreased from their initial status. Compared to year 11, water‐soluble K increased, whereas exchangeable K decreased after year 22 in plots receiving no K fertilizer. Compared with NPK treatments, a significant decrease of total K in NP treatment plots suggests the release and uptake of nonexchangeable K. Water‐soluble K and exchangeable K were not correlated with K uptake. These results suggest that long‐term application of P fertilizers resulted in the accumulation of P in the soil, which could have resulted in saturation of P binding sites. Of the soil inorganic P fractions, only chloride P appears to be a good indicator of plant‐available P. The gradual loss in native soil K and release of nonexchangeable K indicates the need for adding K fertilizer to maintain soil fertility.     

Trends in Sulfate,Base Cations and H+ Concentrations in Bulk Precipitation and Throughfall at Integrated Monitoring Sites in Finland 1989-1995

Temporal trends in sulfate, base cation (Ca2+ + Mg2+ + K+), and H+ ion concentrations in bulk precipitation and throughfall samples collected over a seven year period (1989-95) in four forested catchments in Finland are presented. The catchments are in remote locations and span the boreal zone (61-69 °N). The stands represent old, undisturbed forests, and are composed of varying proportions of Scots pine, Norway spruce and deciduous species (mainly Betula spp.). Monthly SO₄ ^2- and H+ ion concentrations in bulk precipitation averaged over the study period and catchments were: 18.7 µmol L^-1 and 32.3 µmol L^-1. The corresponding values for throughfall were: 37.4 µmol L^-1 and 32.4 µmol L^-1. Sulfate and H+ ion concentrations in bulk precipitation and throughfall both showed negative linear trends, which were significant (p < 0.05) for the three southernmost catchments. Concentrations and trend slope decreased northwards (e.g., bulk precipitation SO₄ ^2- slope estimates: ^-1.6 to ^-1.0 µmol L^-1 yr^-1). The decline was greater for throughfall than for bulk precipitation, indicating a proportionally greater reduction in dry deposition than wet. The sum of base cation concentrations averaged 12.1 µmol(+) L^-1 in bulk precipitation and 83.1 µmol(+) L^-1 in throughfall. There were no significant trends in the sum of base cations (p > 0.05). It is concluded that the reported reduction in S emissions over the study period has resulted in a significant reduction in the acidity and SO₄ ^2- concentration of bulk precipitation, and this reduction has has been reflected in throughfall concentrations. The greatest reduction has taken place in the southern part of the country.     

时空亏缺调控灌溉和施氮处理对番茄水氮利用的影响

为探索节水灌溉条件下蔬菜的水肥高效利用模式, 采用番茄盆栽试验, 以常规充分灌水为对照, 研究了时空亏缺调控灌溉和氮肥处理对番茄营养器官干物质累积、灌溉水分利用效率、氮素累积及土壤水氮分布的影响。在交替灌溉条件下, 设置控水时期、灌水水平和施氮水平3因素, 控水时期分别为开花座果期和结果期, 2个灌水水平分别为高水和低水, 3个施氮水平分别为高氮、低氮和无氮, 并以常规灌溉作为对照。结果表明: 与常规充分灌水处理相比, 交替灌溉持续高水处理、交替灌溉开花座果期低水处理、交替灌溉结果期低水处理及交替灌溉持续低水处理分别降低干物质累积总量4.52%、11.93%、17.76%和23.94%, 分别降低氮素累积总量1.74%、12.86%、15.50%和22.47%, 分别降低氮素干物质生产效率2.24%、3.93%、2.55%和0.89%, 而分别增加灌溉水分利用效率12.39%、8.99%、15.02%和12.96%。在交替灌溉条件下, 中氮处理的干物质累积、灌溉水分利用效率和氮素累积总量最大。与低氮处理相比, 中氮和高氮处理的氮素干物质生产效率分别降低6.87%~12.70%和17.81%~24.38%, 土壤硝态氮分别提高31.64%~159.58%和57.37%~297.37%。综合考虑干物质累积、水分利用及氮素累积等因素, 番茄适宜的水氮供给模式为交替灌溉持续高水中氮处理: 灌水定额为80%W₀(W₀为常规充分灌溉的灌水定额, 保持土壤含水量为田间持水量的70%~85%), 施氮量为0.30 g(N)·kg^-1(干土)。     

Evaluation of Extractants and Quantity–Intensity Relationship for Estimation of Available Potassium in Some Calcareous Soils of Western Iran

Accurate estimation of the available potassium (K⁺) supplied by calcareous soils in arid and semi‐arid regions is becoming more important. Exchangeable K⁺, determined by ammonium acetate (NH₄OAc), might not be the best predictor of the soil K⁺ available to crops in soils containing micaceous minerals. The effectiveness of different extraction methods for the prediction of K‐supplying capacities and quantity–intensity relationships was studied in 10 calcareous soils in western Iran. Total K⁺ uptake by wheat grown in the greenhouse was used to measure plant‐available soil K⁺. The following methods extracted increasingly higher average amounts of soil K⁺: 0.025 M H₂SO₄ (45 mg K⁺ kg^?1), 1 M NaCl (92 mg K⁺ kg^?1), 0.01 M CaCl₂ (104 mg K⁺ kg^?1), 0.1 M BaCl₂ (126 mg K⁺ kg^?1), and 1 M NH₄OAc (312 mg K⁺ kg^?1). Potassium extracted by 0.01 M CaCl₂, 1 M NaCl, 0.1 M BaCl₂, and 0.025 M H₂SO₄ showed higher correlation with K⁺ uptake by the crop (P < 0.01) than did NH₄OAc (P < 0.05), which is used to extract K⁺ in the soils of the studied area. There were significant correlations among exchangeable K⁺ adsorbed on the planar surfaces of soils (labile K⁺) and K⁺ plant uptake and K⁺ extracted by all extractants. It would appear that both 0.01 M CaCl₂ and 1 M NaCl extractants and labile K⁺ may provide the most useful prediction of K⁺ uptake by plants in these calcareous soils containing micaceous minerals.     

Temporal in situ dynamics of N<Subscript>2</Subscript>O reductase activity as affected by nitrogen fertilization and implications for the N<Subscript>2</Subscript>O/(N<Subscript>2</Subscript>O + N<Subscript>2</Subscript>) product ratio and N<Subscript>2</Subscript>O mitigation

In vitro, high nitrate (NO₃ ^?) concentrations significantly inhibit N₂O reductase activity. However, little information is available on the in situ temporal effects of excessive N fertilization on soil N₂O reductase activity and the regulation of the N₂O/(N₂ + N₂O) product ratio in agricultural soil. This study examined the monthly in situ dynamics of NO₃ ^? concentration, N₂O reductase activity, and N₂O/(N₂ + N₂O) product ratio for 2 years in loamy soil that had received either continuous N fertilizer at 400 kg N ha^?1 year^?1 for 15 years (N400) or no N fertilizers (CK). N₂O reductase activity was significantly lower under the N400 treatment than under the CK and correlated negatively with soil NO₃ ^? concentration. The decrease in N₂O reductase activity resulted in the N₂O/(N₂ + N₂O) product ratio increasing. These results demonstrate that excessive N fertilization has the potential to increase N₂O emissions by reducing N₂O reductase activity in soils. These results highlight the need for N₂O mitigation options to embrace the reduction of soil NO₃ ^? concentrations.     

Relationships between microbial biomass nitrogen,nitrate leaching and nitrogen uptake by corn in a compost and chemical fertilizer-amended regosol

Abstract

To determine the relationships between microbial biomass nitrogen (N), nitrate–nitrogen leaching (NO₃-N leaching) and N uptake by plants, a field experiment and a soil column experiment were conducted. In the field experiment, microbial biomass N, 0.5 mol L^?1 K₂SO₄ extractable N (extractable N), NO₃-N leaching and N uptake by corn were monitored in sawdust compost (SDC: 20 Mg ha^?1 containing 158 kg N ha^?1 of total N [approximately 50% is easily decomposable organic N]), chemical fertilizer (CF) and no fertilizer (NF) treatments from May 2000 to September 2002. In the soil column experiment, microbial biomass N, extractable N and NO₃-N leaching were monitored in soil treated with SDC (20 Mg ha^?1) + rice straw (RS) at five different application rates (0, 2.5, 5, 7.5 and 10 Mg ha^?1 containing 0, 15, 29, 44 and 59 kg N ha^?1) and in soil treated with CF in 2001. Nitrogen was applied as (NH₄)₂SO₄ at rates of 220 kg N ha^?1 for SDC and SDC + RS treatments and at a rate of 300 kg N ha^?1 for the CF treatment in both experiments. In the field experiment, microbial biomass N in the SDC treatment increased to 147 kg N ha^?1 at 7 days after treatment (DAT) and was maintained at 60–70 kg N ha^?1 after 30 days. Conversely, microbial biomass N in the CF treatment did not increase significantly. Extractable N in the surface soil increased immediately after treatment, but was found at lower levels in the SDC treatment compared to the CF treatment until 7 DAT. A small amount of NO₃-N leaching was observed until 21 DAT and increased markedly from 27 to 42 DAT in the SDC and CF treatments. Cumulative NO₃-N leaching in the CF treatment was 146 kg N ha^?1, which was equal to half of the applied N, but only 53 kg N ha^?1 in the SDC treatment. In contrast, there was no significant difference between N uptake by corn in the SDC and CF treatments. In the soil column experiment, microbial biomass N in the SDC + RS treatment at 7 DAT increased with increased RS application. Conversely, extractable N at 7 DAT and cumulative NO₃-N leaching until 42 DAT decreased with increased RS application. In both experiments, microbial biomass N was negatively correlated with extractable N at 7 DAT and cumulative NO₃-N leaching until 42 DAT, and extractable N was positively correlated with cumulative NO₃-N leaching. We concluded that microbial biomass N formation in the surface soil decreased extractable N and, consequently, contributed to decreasing NO₃-N leaching without impacting negatively on N uptake by plants.     

Nitrogen fixation as influenced by moisture content,ammonium sulphate and organic sources in a paddy soil

The effect of moisture and (NH₄)₂SO₄ on N₂ fixation in a paddy soil was investigated employing C₂H₂ reduction assay and ¹⁵N-tracers. N₂ fixation was negligible under nonflooded conditions. Soil submergence accelerated N₂ fixation; with a further increase in N₂ fixation when the flooded soil was incubated under an Ar atmosphere. Rice straw additions to both moist and flooded soils enhanced N₂ fixation. N₂-ase activity in the soil decreased with increasing concentration of added N although complete suppression of the activity was not evident even at concentrations as high as 160–320 parts/10⁶ N. A similar trend of inhibition by N was also noticed in soils amended with glucose or cellulose in combination with N. However, the inhibitory effect of N decreased with increased incubation of soil except at 320 parts/10⁶ N.