Effect of the non-fertilizer N supply of grassland soils on the response of herbage to N fertilization under mowing conditions

I tested whether the non-fertilizer N supply of grassland soils (NFNS; N uptake on unfertilized plots) affects the relationships between N uptake and dry matter production, N application and N uptake, N application and dry matter production, as well as the optimum fertilizer application rate.At low N uptake rates the amount of dry matter production per kg of N uptake was negatively correlated with NFNS; at higher N uptake levels the correlation was not significant. The apparent nitrogen recovery of fertilizer N was not correlated with NFNS. The optimum fertilizer application rate was correlated positively with the maximum dry matter production (Max DM) and negatively with NFNS. The relationship optimum fertilizer application = –81–0.8 × NFNS + 0.0375 × Max DM accounted for 89% of the variance in optimum fertilizer application rate between soils at a marginal N effect of 7.5 kg dry matter per kg N applied. So an increase in NFNS of 100 kg N resulted in a decrease of the optimum N application rate of 80 kg N.     

Assessment of the C/N ratio as an indicator of the decomposability of organic matter in forest soils

The usefulness of the C/N ratio as an indicator of the decomposability of organic matter in forest soil was assessed. The assessment was based on the relationship between the C/N ratio and the contents of soil organic carbon (SOC), soil nitrogen (total N), dissolved total organic carbon (DTOC) and dissolved inorganic nitrogen (DIN). SOC, total N, DTOC and DIN were determined in soils sampled in coniferous and coniferous–deciduous forest sites from genetic horizons of 48 soil profiles. The variability of the above soil parameters was determined and the correlation between these parameters and the C/N values were calculated. It was found that the C/N ratio in soil was shaped by the difference in the mobility of both elements, whereas the decrease in the C content in subsequent horizons was mostly higher than the decrease in the N content, which means that the C/N value decreased with the depth of a soil profile. When the loss of SOC and total N contents occurs at a similar rate, the C/N ratio is maintained at a more or less stable level despite the advancing SOM mineralization. When the rate of the carbon release from SOM differs from that of nitrogen or when there is an N input from external sources, the C/N ratio does not adequately describe the process of SOM mineralization as well. The correlation coefficients between the C/N ratio and other parameters indicate that the relationships between them are not significant or that there is no correlation at all. It was found that the percentage of DTOC in SOC seemed to be a better indicator of SOM mineralization than the C/N ratio.     

Effects of cattle slurry and mineral N fertilizer applications on various components of the nitrogen balance of mown grassland

It is essential to establish more accurate N balances for different soil-plant systems in order to improve N use efficiency. In this study the N balance was studied in a poorly drained clayey loam soil under natural grassland supplied with either calcium ammonium nitrate or cattle slurry at two application rates. The aim was to determine the efficiency of the N applied and the factors which affect this efficiency. Mineralization-immobilization of N was calculated by balance between the quantified inputs and outputs of N. As N inputs increased, output via herbage yield was accompanied by an increase in apparent immobilization of N in the soil and by larger losses of N by denitrification. The difference between cattle slurry and N fertilizer was that the slurry behaved as a slow release fertilizer, its supply of mineral N being greater in the periods of time when fertilizer was applied a long time ago. Denitrification losses (up to 17% of the N applied) are suggested to be the main factor to mitigate in order to increase N use efficiency. A decrease in net mineralization (up to 136 kg N ha^-1 year^-1) was observed which was related to the mineral N application rate. There was evidence to suggest that this decrease was due both to the immobilization of the N applied and to a decrease in the rate of gross mineralization when mineral N was applied. Microbial biomass determinations could not explain the changes in the mineralization-immobilization equilibrium of N because of the great coefficients of variation for this determination (mean value of 18%). Nevertheless, it contributed to verify and explain some of the changes observed in this equilibrium.     

Legumes regulate grassland soil N cycling and its response to variation in species diversity and N supply but not CO2

Legumes are an important component of plant diversity that modulate nitrogen (N) cycling in many terrestrial ecosystems. Limited knowledge of legume effects on soil N cycling and its response to global change factors and plant diversity hinders a general understanding of whether and how legumes broadly regulate the response of soil N availability to those factors. In a 17‐year study of perennial grassland species grown under ambient and elevated (+180 ppm) CO₂ and ambient and enriched (+4 g N m^?2 year^?1) N environments, we compared pure legume plots with plots dominated by or including other herbaceous functional groups (and containing one or four species) to assess the effect of legumes on N cycling (net N mineralization rate and inorganic N pools). We also examined the effects of numbers of legume species (from zero to four) in four‐species mixed plots on soil N cycling. We hypothesized that legumes would increase N mineralization rates most in those treatments with the greatest diversity and the greatest relative limitation by and competition for N. Results partially supported these hypotheses. Plots with greater dominance by legumes had greater soil nitrate concentrations and mineralization rates. Higher species richness significantly increased the impact of legumes on soil N metrics, with 349% and 505% higher mineralization rates and nitrate concentrations in four‐species plots containing legumes compared to legume‐free four‐species plots, in contrast to 185% and 129% greater values, respectively, in pure legume than nonlegume monoculture plots. N‐fertilized plots had greater legume effects on soil nitrate, but lower legume effects on net N mineralization. In contrast, neither elevated CO₂ nor its interaction with legumes affected net N mineralization. These results indicate that legumes markedly influence the response of soil N cycling to some, but not all, global change drivers.     

Sorption of dissolved organic matter by mineral soils of the Siberian forest tundra

Because of low net production in arctic and subarctic surface water, dissolved organic matter (DOM) discharged from terrestrial settings plays an important role for carbon and nitrogen dynamics in arctic aquatic systems. Sorption, typically controlling the export of DOM from soil, may be influenced by the permafrost regime. To confirm the potential sorptive control on the release of DOM from permafrost soils in central northern Siberia, we examined the sorption of DOM by mineral soils of Gelisols and Inceptisols with varying depth of the active layer. Water‐soluble organic matter in the O horizons of the Gelisols was less (338 and 407 mg C kg^?1) and comprised more dissolved organic carbon (DOC) in the hydrophobic fraction (HoDOC) (63% and 70%) than in the O horizons of the Inceptisols (686 and 706 mg C kg^?1, 45% and 48% HoDOC). All A and B horizons from Gelisols sorbed DOC strongly, with a preference for HoDOC. Almost all horizons of the Inceptisols showed a weaker sorption of DOC than those of the Gelisols. The C horizons of the Inceptisols, having a weak overall DOC sorption, sorbed C in the hydrophilic fraction (HiDOC) stronger than HoDOC. The reason for the poor overall sorption and also the preferential sorption of HiDOC is likely the high pH (pH>7.0) of the C horizons and the smaller concentrations of iron oxides. For all soils, the sorption of HoDOC related positively to oxalate‐ and dithionite–citrate‐extractable iron. The A horizons released large amounts of DOC with 46–80% of HiDOC. The released DOC was significantly (r=0.78, P<0.05) correlated with the contents of soil organic carbon. From these results, we assume that large concentrations of DOM comprising large shares of HiDOC can pass mineral soils where the active layer is thin (i.e. in Gelisols), and enter streams. Soils with deep active layer (i.e. Inceptisols), may release little DOM because of more frequent infiltration of DOM into their thick mineral horizons despite their smaller contents of reactive, poorly crystalline minerals. The results obtained for the Inceptisols are in agreement with the situation observed for streams connecting to Yenisei at lower latitudes than 65°50′ with continuous to discontinuous permafrost. The smaller sorption of DOM by the Gelisols is in agreement with the larger DOM concentrations in more northern catchments. However, the Gelisols preferentially retained the HoDOC which dominates the DOC in streams towards north. This discrepancy can be explained by additional seepage water from the organic horizons that is discharged into streams without intensive contact with the mineral soil.     

Significance of nitrate leaching and long term N immobilization after deepening the plough layers for the N regime of arable soils in N.W. Germany

Field studies were conducted to assess the turnover and the leaching of nitrogen in arable soils of Lower Saxony (NW Germany). The mean surplus N (difference between N inputs by fertilization and N export by the yield; 146 field plots) from 1985–1988 amounted to 38 kg ha^-1 yr^-1 in fine textured (clay, loam, silt) and to 98 kg ha^-1 yr^-1 in coarse (sandy) soils. Leaching of nitrate calculated by a simple functional model for simulation of the N regime over the winter period (i.e. mineralization and leaching) was 16 kg ha^-1 in the fine and 63 kg N ha^-1 in coarse soils (mean values of the winter periods 1985–1988 from 256 plots).Before the 1960s, the depth of the A_p horizons rarely exceeded 25 cm in arable soils of the former FRG. During the last three decades, ploughing depth has increased to at least 35 cm. The mass balance calculations for total N after ploughing to 35 cm in loess soils of southern Lower Saxony (105 farm plots) yielded a mean increase in total N by about 900 kg ha^-1 in 20 years. With respect to soil organic matter equilibria, N accumulation will continue for at least another 10 years on 67% of the examined farm plots. This study suggests that long term N immobilization is one of the most important sinks for nitrogen in arable soils of Germany. For simulation of the N dynamics over the growing season and for long time periods total nitrogen dynamics need to be considered.     

Dynamics of C,N, P and S in grassland soils: a model

We have developed a model to simulate the dynamics of C, N, P, and S in cultivated and uncultivated grassland soils. The model uses a monthly time step and can simulate the dynamics of soil organic matter over long time periods (100 to 10,000 years). It was used to simulate the impact of cultivation (100 years) on soil organic matter dynamics, nutrient mineralization, and plant production and to simulate soil formation during a 10,000 year run. The model was validated by comparing the simulated impact of cultivation on soil organic matter C, N, P, and S dynamics with observed data from sites in the northern Great Plains. The model correctly predicted that N and P are the primary limiting nutrients for plant production and simulated the response of the system to inorganic N, P, and S fertilizer. Simulation results indicate that controlling the C:P and C:S ratios of soil organic matter fractions as functions of the labile P and S levels respectively, allows the model to correctly simulate the observed changes in C:P and C:S ratios in the soil and to simulate the impact of varying the labile P and S levels on soil P and S net mineralization rates.     

黄土高原典型土壤有机氮矿化过程

以黄土高原从北向南不同地区典型土壤类为对象,采用Bremner淹水培养法,研究黄土高原典型土壤有机氮的矿化过程。结果表明,淹水培养期间矿化出的部分NH4^＋-N会被粘土矿物固定,固定量因土壤不同而异,因此在测定有机氮矿化量时,只有考虑这一部分氮素,才可获得可靠结果。不同土壤有机氮量矿化明显不同,表现为土垫旱耕人为土〉黄土正常新成土〉简育干润均腐土〉干润砂质新成土,从南到北氮素矿化量呈减小趋势。添加C／N低（C／N比为21．7）的紫花苜蓿（Medicago stativa）茎叶有利于促进土壤有机氮矿化,而添加C／N高（C／N比为43．3）的长芒草（Stipa bungeana）会促进矿质氮的生物固定;不同类型植被土壤间在培养20、40d和60d时的矿化量差异显著（P值分别为0．0177、0．0109和0．0073）,均表现为均为林地土壤〉裸地土壤〉草地土壤〉农田土壤;从平均看,加（NH4）2SO4后有机氮矿化量有一定减少。在不同培养阶段,不同土类间氮素矿化率不同,在20d和40d时存在显著差异（P分别为0．0092和0．0381）,60d时差异不显著,不同土类氮素矿化率的大小顺序为于润砂质新成土〉黄土正常新成土〉土垫旱耕人为土〉简育干润均腐土,这一结果说明在淹水条件下,黄土高原土壤从南到北易矿化氮所占全氮比例呈增加趋势。     

In situ studies of soil mineral N fluxes: Some comments on the applicability of the sequential soil coring method in arable soils

Is the sequential in situ incubation of undisturbed soil cores, developed for forest stands applicable to arable soils? The incubation of covered and uncovered soil cores allows the estimation of net nitrogen mineralization (NNM), plant nitrogen uptake (N_uptake) and potential leaching losses (N_trans). The amounts and temporal dynamics of these N fluxes were determined at four arable soils in a two-year study. Results suggest that: (i) the method can not be recommended for the estimation of N uptake and leaching losses, but (ii) it is suitable for the estimation of NNM; (iii) incubations should preferably be started when soil is moist; (iv) the length of incubation periods should be reduced (<4 weeks); (v) dynamics of NNM is mainly determined by temperature and moisture conditions if there is no interference by agricultural management. Inputs of straw, manure, slurry or green manure strongly influence the amount and the dynamics of NNM.     

Reappraisal of drying and wetting effects on C and N mineralization and fluxes in soils

In the next decades, many soils will be subjected to increased drying/wetting cycles or modified water availability considering predicted global changes in precipitation and evapotranspiration. These changes may affect the turnover of C and N in soils, but the direction of changes is still unclear. The aim of the review is the evaluation of involved mechanisms, the intensity, duration and frequency of drying and wetting for the mineralization and fluxes of C and N in terrestrial soils. Controversial study results require a reappraisal of the present understanding that wetting of dry soils induces significant losses of soil C and N. The generally observed pulse in net C and N mineralization following wetting of dry soil (hereafter wetting pulse) is short‐lived and often exceeds the mineralization rate of a respective moist control. Accumulated microbial and plant necromass, lysis of live microbial cells, release of compatible solutes and exposure of previously protected organic matter may explain the additional mineralization during wetting of soils. Frequent drying and wetting diminishes the wetting pulse due to limitation of the accessible organic matter pool. Despite wetting pulses, cumulative C and N mineralization (defined here as total net mineralization during drying and wetting) are mostly smaller compared with soil with optimum moisture, indicating that wetting pulses cannot compensate for small mineralization rates during drought periods. Cumulative mineralization is linked to the intensity and duration of drying, the amount and distribution of precipitation, temperature, hydrophobicity and the accessible pool of organic substrates. Wetting pulses may have a significant impact on C and N mineralization or flux rates in arid and semiarid regions but have less impact in humid and subhumid regions on annual time scales. Organic matter stocks are progressively preserved with increasing duration and intensity of drought periods; however, fires enhance the risk of organic matter losses under dry conditions. Hydrophobicity of organic surfaces is an important mechanism that reduces C and N mineralization in topsoils after precipitation. Hence, mineralization in forest soils with hydrophobic organic horizons is presumably stronger limited than in grassland or farmland soils. Even in humid regions, suboptimal water potentials often restrict microbial activity in topsoils during growing seasons. Increasing summer droughts will likely reduce the mineralization and fluxes of C and N whereas increasing summer precipitation could enhance the losses of C and N from soils.     

Dynamics of mineral N availability in grassland ecosystems under increased [CO2]: hypotheses evaluated using the Hurley Pasture Model

The following arguments are outlined and then illustrated by the response of the Hurley Pasture Model to [CO₂] doubling in the climate of southern Britain. 1. The growth of N-limited vegetation is determined by the concentration of N in the soil mineral N pools and high turnover rates of these pools (i.e., large input and output fluxes) contribute positively to growth. 2. The size and turnover rates of the soil mineral N pools are determined overwhelmingly by N cycling into all forms of organic matter (plants, animals, soil biomass and soil organic matter — `immobilisation' in a broad sense) and back again by mineralisation. Annual system N gains (by N₂ fixation and atmospheric deposition) and losses (by leaching, volatilisation, nitrification and denitrification) are small by comparison. 3. Elevated [CO₂] enriches the organic matter in plants and soils with C, which leads directly to increased removal of N from the soil mineral N pools into plant biomass, soil biomass and soil organic matter (SOM). ‘Immobilisation’ in the broad sense then exceeds mineralisation. This is a transient state and as long as it exists the soil mineral N pools are depleted, N gaseous and leaching losses are reduced and the ecosystem gains N. Thus, net immobilisation gradually increases the N status of the ecosystem. 4. At the same time, elevated [CO₂] increases symbiotic and non-symbiotic N₂ fixation. Thus, more N is gained each year as well as less lost. Effectively, the extra C fixed in elevated [CO₂] is used to capture and retain more N and so the N cycle tracks the C cycle. 5. However, the amount of extra N fixed and retained by the ecosystem each year will always be small (ca. 5–10 kg N ha^-1 yr^-1) compared with amount of N in the immobilisation-mineralisation cycle (ca. 1000 kg N ha^-1 yr^-1). Consequently, the ecosystem can take decades to centuries to gear up to a new equilibrium higher-N state. 6. The extent and timescale of the depletion of the mineral N pools in elevated [CO₂] depends on the N status of the system and the magnitude of the overall system N gains and losses. Small changes in the large immobilisation—mineralisation cycle have large effects on the small mineral N pools. Consequently, it is possible to obtain a variety of growth responses within 1–10 year experiments. Ironically, ecosystem models — artificial constructs — may be the best or only way of determining what is happening in the real world. This revised version was published online in June 2006 with corrections to the Cover Date.     

Elevated [CO2], temperature increase and N supply effects on the accumulation of below-ground carbon in a temperate grassland ecosystem

The effects of elevated [CO₂] (700 μl l⁻¹ [CO₂]) and temperature increase (+3 °C) on carbon accumulation in a grassland soil were studied at two N-fertiliser supplies (160 and 530 kgN ha⁻¹ year⁻¹) in a long-term experiment (2.5 years) on well established ryegrass swards (Lolium perenne L.,) supplied with the same amounts of irrigation water. For all experimental treatments, the C:N ratio of the top soil organic matter fractions increased with their particle size. Elevated CO₂ concentration increased the C:N ratios of the below-ground phytomass and of the macro-organic matter. A supplemental fertiliser N or a 3 °C increase in elevated [CO₂] reduced it. At the last sampling date, elevated [CO₂] did not affect the C:N ratio of the soil organic matter fractions, but increased significantly the accumulation of roots and of macro-organic matter above 200 μm (MOM). An increased N-fertiliser supply stimulated the accumulation of the non harvested plant phytomass and of the OM between 2 and 50 μm, without positive effect on the macro-organic matter >200 μm. Elevated [CO₂2] increased C accumulation in the OM fractions above 50 μm by +2.1 tC ha⁻¹, on average, whereas increasing the fertiliser N supply led to an average supplemental accumulation of +0.8 tC ha⁻¹. There was no significant effect of a 3 °C temperature increase under elevated [CO₂] on C accumulation in the OM fractions above 50 μm. This revised version was published online in June 2006 with corrections to the Cover Date.     

Modelling the change in soil organic C and N and the mineralization of N from soil in response to applications of slurry manure

A computer simulation model of the turnover of organic matter in soil was adapted to simulate the change in soil organic C and N contents of soil during several years following annual additions of farm slurry to maize fields. The model proved successful in estimating the build-up of both C and N in soil and the leaching of N to ground-water in response to applications of slurry ranging from 50 to 300 tons per hectare per year. The model was then used to estimate the build-up of organic matter in soil under crops of fodder maize that were grown using the excess of manure produced during the last 20 years in the Netherlands. The build-up of organic matter from these applications was estimated to lead to about 70 kg extra nitrogen mineralized ha^-1 yr^-1. As a result of legislation manure applications have decreased and are expected to decrease further in the immediate future. Calculations suggest that after 10 years of manure applied at rates no longer exceeding the amount needed to replace the phosphorus removed by crops, the extra mineralization of N will still be between 45 and 60 kg ha^-1 yr^-1. If manure applications cease altogether then the extra mineralization will be about 25–30 kg N ha^-1 yr^-1.     

Nitrogen mineralization dynamics in grass monocultures

Although Wedin and Tilman (1990) observed large differences in in situ N mineralization among monocultures of five grass species, the mechanisms responsible were unclear. In this study, we found that the species did not change total soil C or N, and soil C: N ratio (range 12.9–14.1) was only slightly, but significantly, changed after four years. Nor did the species significantly affect the total amount of N mineralized (per g soil N) in year-long aerobic laboratory incubations. However, short-term N mineralization rates in the incubations (day 1–day 17) differed significantly among species and were significantly correlated with annual in situ mineralization. When pool sizes and turnover rates of potentially mineralizable N (N_o) were estimated, the best model treated N_o as two pools: a labile pool, which differed among species in size (N_l, range 2–3% of total N) and rate constant (h, range 0.04–0.26 wk^–1), and a larger recalcitrant pool with a constant mineralization rate across species. The rate constant of the labile pool (h) was highly correlated with annual in situ N mineralization (+0.96). Therefore, plant species need only change the dynamics of a small fraction of soil organic matter, in this case estimated to be less than 3%, to have large effects on overall system N dynamics.     

Disentangling species and functional group richness effects on soil N cycling in a grassland ecosystem

Species richness (SR) and functional group richness (FGR) are often confounded in both observational and experimental field studies of biodiversity and ecosystem function. This precludes discernment of their separate influences on ecosystem processes, including nitrogen (N) cycling, and how those influences might be moderated by global change factors. In a 17‐year field study of grassland species, we used two full factorial experiments to independently vary SR (one or four species, with FGR = 1) and FGR (1–4 groups, with SR = 4) to assess SR and FGR effects on ecosystem N cycling and its response to elevated carbon dioxide (CO₂) and N addition. We hypothesized that increased plant diversity (either SR or FGR) and elevated CO₂ would enhance plant N pools because of greater plant N uptake, but decrease soil N cycling rates because of greater soil carbon inputs and microbial N immobilization. In partial support of these hypotheses, increasing SR or FGR (holding the other constant) enhanced total plant N pools and decreased soil nitrate pools, largely through higher root biomass, and increasing FGR strongly reduced mineralization rates, because of lower root N concentrations. In contrast, increasing SR (holding FGR constant and despite increasing total plant C and N pools) did not alter root N concentrations or net N mineralization rates. Elevated CO₂ had minimal effects on plant and soil N metrics and their responses to plant diversity, whereas enriched N increased plant and soil N pools, but not soil N fluxes. These results show that functional diversity had additional effects on both plant N pools and rates of soil N cycling that were independent of those of species richness.     

温带草甸草原土壤N2O产生过程研究

以大量的室内模拟培养实验,以内蒙古温带草甸草原土壤为研究对象,利用AIM乙炔抑制法,模拟野外条件对原样土壤样品进行N₂O产生过程进行研究。实验结果表明:内蒙古温带草甸草原土壤N₂O产生过程以硝化作用为主。其中异养硝化作用起主导作用,自养硝化潜势和反硝化潜势在草原植物不同生长季节变化不同,总体上异养硝化潜势>自养硝化潜势>反硝化潜势。由于自养硝化作用在不同季节的发生,使得草甸草原土壤N₂O的产生潜势也高、低起伏变化。从而揭示了内蒙古温带草原土壤以异养硝化作用过程为主产生N₂O和N₂O排放通量较低的微生物学机理。     

Failure of an iterative curve-fitting procedure to successfully estimate two organic N pools

Fitting a double negative exponential function to N mineralization data can be used to characterize two organic nitrogen pools; an easily decomposable (N_dpm) and a resistant one (N_rpm). The relevance of those two calculated N mineralization pools was investigated by adding easily decomposable organic material to soils. Soil amended with crop residues of sugar-beet or bean was mixed with an equal amount of coarse sand, incubated at 35 °C and leached at specific time-intervals. Upon leaching, NH₄ ⁺ and NO₃ ^- were measured in the extracts. A double negative exponential function was fitted to the data and two organic N pools were defined. Fitting a double negative exponential function to N mineralization data to characterize an active and resistant organic N pool was sometimes impossible; the N mineralization data did not always resemble a negative exponential function. Additionally, the size of the two pools calculated were not constant with time and were often meaningless; the N_rpm pool was greater than the soil organic N content, the size of the N_rpm pool was smaller than the N_dpm pool or one of the N pools was negative. Relevant values for both N_rpm and N_dpm which were consistent with incubation time were only obtained when excessive amounts of organic material, normally not dealt with in the field, were applied.     

Prediction of long-term fertilizer nitrogen requirements of maize in the tropics using a nitrogen balance model

A simple N balance model was used to calculate fertilizer requirement for a target N uptake by maize. Nitrogen uptake from soil sources and target uptake of N with fertilizer N additions were obtained from fertilizer trials in Africa and Latin America. Most experiments had data for only one cropping period, although some from Latin America had data for four to six crops. The transfer coefficient of fertilizer N to the crop was adjusted to realize maximum recovery of fertilizer N under best methods of fertilizer application. The time constants of transfer of soil N to the crop were allowed to vary and were affected mainly by soil texture. Where 4 to 6 cropping periods were available good agreement between actual and predicted fertilizer N requirements was obtained. With this approach long-term fertilizer N requirements for 14 sites were predicted using first cropping period N uptake. This study showed that pools of organic N in more coarse-textured soils were usually smaller and declined more rapidly than in fine-textured soils. Labile organic N pools declined with time under all simulations, but approached equilibrium within 10 croppings seasons. Equilibrium N uptake from the soil organic N pool was predicted to be 31 kg ha^–1 for the more coarse-textured soils and 36 kg ha^–1 for the fine-textured soils. Long-term projections of fertilizer requirements using input data of the field experiments were reasonable, and effects of legume green manures and other amendments could be clearly evaluated.     

Prediction of nitrogen availability and rice yield in lowland soils: Nitrogen mineralization parameters

Field experiments were conducted under flooded soil conditions using Maahas clay amended with urea and rice straw-sesbania mixtures during the wet and dry seasons. Parallel laboratory incubation tests were done. The objectives were 1) to determine N mineralization patterns and establish the relationship between mineralization parameters and either N availability or grain yield, and 2) to correlate the results of organic N mineralization studies in the laboratory with data from field experiments. The N mineralization patterns of flooded soils in the laboratory followed a logistic function. In laboratory studies, mineralization potential was positively correlated with extractable soil NH₄ ⁺-N at the end of the incubation period (cumulative available N). Likewise, mineralization potential calculated from laboratory studies was positively correlated with N uptake and grain yield from field studies. Extractable (NH₄ ⁺+NO₃ ^–)-N in the field correlated positively with extractable NH₄ ⁺-N in the laboratory. The extractable NH₄ ⁺-N from laboratory incubations at 14 days after transplanting, panicle initiation, and maturity was also highly and positively correlated with grain yield from field experiments.