Field measurement of nitrogen mineralization using soil core incubation and acetylene inhibition of nitrification

A technique for measuring net rates of mineralization under field conditions is described. Soil cores were incubated in the field in sealed containers with acetylene to inhibit nitrification and thereby minimize losses of N through denitrification. Mineralization was estimated as the difference between the mineral N content after a 14-d incubation and that determined from soil samples taken at the start of incubation. Mineralization in the spring and summer in unfertilized plots in the field amounted to 90 and 70 kg N ha⁻¹ in S.E. England under grass and grass/clover swards, respectively, and 40 kg N ha⁻¹ under a grass sward in S.W. England. Daily rates of mineralization ranged from 0.02 to 1.90 kg N ha⁻¹, with peak values related to re-wetting of the soil after dry weather. Laboratory incubation of soil showed that neither the low concentration of acetylene (2% v/v) adopted for field incubation, nor the accumulation of mineral N during incubation was likely to affect the total measurement, but that frequent and regular soil sampling was necessary to minimize the effects of changes in soil water content. Estimates for mineralization over the whole growing season (180 d) were obtained for two years from extrapolation of the early season field measurements and were, on average, 50% higher than predictions based on a chemical extraction index of potentially mineralizable N.     

Effects of white clover (Trifolium repens L.) on plant and soil nitrogen and soil organic matter in mixtures with perennial ryegrass (Lolium perenne L.)

To increase our insight into the above- and belowground N flows in grass and grass-clover swards relations between crop and soil parameters were studied in a cutting trial with perennial ryegrass (Lolium perenne) monocultures and ryegrass–white clover (Trifolium repens) mixtures. The effects of clover cultivar on herbage yield, the amount of clover-derived nitrogen, apparent N transfer to companion grass, dynamics of N and organic matter in the soil were estimated.The grass monocultures had very low DM yields (<2.1 t ha^-1) and a low N concentration in the harvested herbage. During 1992–1995 the annual herbage DM yield in the mixtures ranged from 7.0 to 14.3 t ha^-1, the white clover DM yield from 2.4 to 11.2 t ha^-1 and the mean annual clover content in the herbage DM harvested from 34 to 78%. Mixtures with the large-leaved clover cv. Alice yielded significantly more herbage and clover DM and had a higher clover content than mixtures with small/medium-leaved cvs. Gwenda and Retor. Grass cultivar did not consistently affect yield, botanical composition or soil characteristics.The apparent N₂ fixation was very high, ranging from 150 to 545 kg N ha^-1 in the different mixtures. For each tonne of clover DM in the harvested herbage 49 to 63 kg N was harvested, while the apparent N transfer from clover to grass varied between 55 and 113 kg N ha^-1 year^-1.The net N mineralization rate was lower under monocultures than under mixtures. The C mineralization and the amounts of C and N in active soil organic matter fractions were similar for monocultures and mixtures, but the C:N ratio of the active soil organic matter fractions were higher under grass than under mixtures. This explains the lower N mineralization under grass.     

Long- and short-term effects of crop residues on aluminum toxicity,phosphorus availability and growth of pearl millet in an acid sandy soil

Pasture swards containing perennial ryegrass (Lolium perenne L.) alone or with one of five different white clover (Trifolium repens L.) cultivars were examined for production and transfer of fixed nitrogen (N) to grass under dairy cow grazing. Grass-only swards produced 21% less than mixed clover-grass swards during the second year after sowing. Production from grass-only plots under a mowing and clipping removal regime was 44% less than from grass-only plots under grazing. Much of this difference could be attributed to N transfer. In swards without clover, the ryegrass component also decreased in favour of other grasses.The average amount of fixed N in herbage from all clover cultivars was 269 kg N ha^–1 yr^–1. Above-ground transfer of fixed N to grasses (via cow excreta) was estimated at 60 kg N ha^–1 yr^–1. Below-ground transfer of fixed N to grasses was estimated at 70 kg N ha^–1 yr^–1 by ¹⁵N dilution and was similar for all clover cultivars. Thus, about 50% of grass N was met by transfer of fixed N from white clover during the measurement year. Short-term measurements using a ¹⁵N foliar-labelling method indicated that below-ground N transfer was largest during dry summer conditions.     

Mineralization of nitrogen in long-term pasture soils: effects of management

A field incubation technique with acetylene to inhibit nitrification was used to estimate net N mineralization rates in some grassland soils through an annual cycle. Measurements were made on previously long-term grazed pastures on a silty clay loam soil in S.W. England which had background managements of +/– drainage and +/– fertilizer (200 kg N ha^–1 yr^–1). The effect of fertilizer addition on mineralization during the year of measurement was also determined. Small plots with animals excluded, and with herbage clipped and removed were used as treatment areas and measurements were made using an incubation period of 7 days at intervals of 7 or 14 days through the year. Soil temperature, moisture and mineral N contents were also determined. Mineralization rates fluctuated considerably in each treatment. Maximum daily rates ranged from 1.01 to 3.19 kg N ha^–1, and there was substantial net release of N through the winter period (representing, on average, 27% of the annual release). Changes in temperature accounted for 35% of the variability but there was little significant effect of soil moisture. Annual net release of N ranged from 135 kg ha^–1 (undrained soil, no previous or current fertilizer) to 376 (drained soil, +200 kg N ha^–1 yr^–1 previous and current fertilizer addition). Addition of fertilizer N to a previously unfertilized sward significantly increased the net release of N but there was no immediate effect of withholding fertilizer on mineralization during the year in which measurements were made.     

Effect of cultivation on the mineralization of nitrogen in soil

Summary The effect of cultivation (ploughing followed by rotavation) on the mineralization of soil nitrogen was measured at 2 sites on a silt loam soil. Both sites had a predominantly arable cropping history but one had been under grass for the previous 2 years and the other had carried wheat. Mineralization of N was slightly faster in cultivated soil but the difference was only significant at the site previously under grass. At this site cultivated soil contained 7 kg ha^–1 more mineral N than uncultivated soil 2 weeks after treatment, and 9 kg ha^–1 after 6 weeks. The corresponding figures for the site that had grown wheat were 4 and 6 kg N ha^–1.     

Interactions between white clover and ryegrass under contrasting nitrogen availability: N2 fixation,N fertilizer recovery,N transfer and water use efficiency

Seasonal variation in N₂ fixation, N transfer from clover to ryegrass, and soil N absorption in white clover–ryegrass swards were investigated under field conditions over three consecutive years. The plots were established with different seeding ratios of clover and ryegrass and contrasting fertilizer N ranging from 3 to 72 kg ha^-1 year^-1.An initially poor clover population needed at least one growing season to reach the same yield output as an initially well established clover population. The clover content of the sward decreased by the annual application of 72 kg N ha^-1 but not by smaller N dressings.The total amount of atmospherically derived N in clover growing in mixture with ryegrass was, on average over the three years equal to 83, 71, 68 and 60 kg N ha^-1 for the treatments of 3, 24, 48 and 72 kg N ha^-1, respectively. The proportion of atmospherically derived N declined with increasing N application, but never became smaller than 80% of total clover N. The proportion of atmospherically derived N in a pure stand white clover amounted to 60–80% of the total N content, equivalent to 109, 110, 103 and 90 kg N ha^-1 for the treatments of 3, 24, 48 and 72 kg N ha^-1, respectively.Only small amounts of atmospherically derived N was transferred to the associated ryegrass during the first production year, while in each of the following years up to 21 kg ha^-1 was transferred. The average amount of N transferred from clover to ryegrass was equivalent to 3, 16 and 31% of the N accumulated in ryegrass in the first, second and third production year, respectively. Expressed relative to the total amount of fixed N₂ in the clover–ryegrass mixture, the transfer amounted to 3, 17 and 22% in the first, second and third production year, respectively. Thus transfer of atmospherically derived N from clover contributed significantly to the N economy of the associated ryegrass.The clover–ryegrass mixture absorbed constantly higher amount of soil derived N than the pure stands of the two species. Only 11% of the total accumulated fertilizer N and soil derived N in the mixture was contained within the clover component. Lower water use efficiencies for the plants grown in mixture compared to pure stands were mainly related to the increased N uptake in the mixture, with the subsequent increase in growth compared to the pure stands.It is concluded that positive interactions between clover and ryegrass growing in mixture ensure a more efficient fixation of atmospheric N₂ and absorption of fertilizer N and soil derived N than pure stands of the same species.     

Nitrogen fixation by white clover in pastures grazed by dairy cows: Temporal variation and effects of nitrogen fertilization

Effects of rate of nitrogen (N) fertilizer and stocking rate on production and N₂ fixation by white clover (Trifolium repens L.) grown with perennial ryegrass (Lolium perenne L.) were determined over 5 years in farmlets near Hamilton, New Zealand. Three farmlets carried 3.3 dairy cows ha^–1 and received urea at 0, 200 or 400 kg N ha^–1 yr^–1 in 8–10 split applications. A fourth farmlet received 400 kg N ha^–1 yr^–1 and had 4.4 cows ha^–1.There was large variation in annual clover production and total N₂ fixation, which in the 0 N treatment ranged from 9 to 20% clover content in pasture and from 79 to 212 kg N fixed ha^–1 yr^–1. Despite this variation, total pasture production in the 0 N treatment remained at 75–85% of that in the 400 N treatments in all years, due in part to the moderating effect of carry-over of fixed N between years.Fertilizer N application decreased the average proportion of clover N derived from N₂ fixation (P_N; estimated by ¹⁵N dilution) from 77% in the 0 N treatment to 43–48% in the 400 N treatments. The corresponding average total N₂ fixation decreased from 154 kg N ha^–1 yr^–1 to 39–53 kg N ha^–1 yr^–1. This includes N₂ fixation in clover tissue below grazing height estimated at 70% of N₂ fixation in above grazing height tissue, based on associated measurements, and confirmed by field N balance calculations. Effects of N fertilizer on clover growth and N₂ fixation were greatest in spring and summer. In autumn, the 200 N treatment grew more clover than the 0 N treatment and N₂ fixation was the same. This was attributed to more severe grazing during summer in the 0 N treatment, resulting in higher surface soil temperatures and a deleterious effect on clover stolons.In the 400 N treatments, a 33% increase in cow stocking rate tended to decrease P_N from 48 to 43% due to more N cycling in excreta, but resulted in up to 2-fold more clover dry matter and N₂ fixation because lower pasture mass reduced grass competition, particularly during spring.     

Changes in soil mineral nitrogen during and after 3-year and 5-year set-aside and nitrate leaching losses after ploughing out the 5-year plant covers in the UK

The management and effects of 3-year and 5-year set-aside covers on soil mineral nitrogen (SMN, 0.0–0.9 m) were studied at six sites in England. Soil mineral N was measured annually in autumn and spring during the period of set-aside cover, with more frequent SMN sampling over the first winter after ploughing out the covers. Spring SMN was measured in the second year after set-aside. Nitrate leaching losses were also measured at three sites in the first winter after destruction of the 5-year set-aside covers. Winter cereals were grown in both test years after each set-aside period.Amounts of both autumn and spring SMN in the perennial rye-grass (PRG), perennial rye-grass/white clover (PRG/WC) and natural regeneration (NR) covers were generally less than, or similar to those in the continuous arable treatment during each year of set-aside, indicating a slightly smaller nitrate leaching risk under set-aside management. Slight increases in autumn SMN, and hence leaching potential were, however, observed under PRG/WC in the fourth and fifth years, compared with continuous arable cropping.Ploughing out of both 3-year and 5-year covers increased soil N supply and potential nitrate leaching losses over winter, compared with continuous arable cropping. By the following spring, mean increases across all sites in amounts of SMN after 3-year covers of PRG, NR and PRG/WC were 14, 18 and 33 kg ha^–1 N, respectively, compared with the arable rotation. Equivalent increases in spring SMN following destruction of the 5-year set-aside covers were almost identical, at 17, 19 and 33 kg ha^–1, respectively, although only the ploughed-out PRG/WC covers increased SMN at the clay sites. Measured nitrate leaching losses in the first winter after 5-year set-aside were greatest after PRG/WC at two sites on shallow chalk but greatest after NR, which had a naturally large clover content, at the third site which was on a sandy soil. However, the leaching losses after set-aside were relatively small, relative to typical losses after ploughing out intensively managed grass or grass/clover swards, and would have been compensated for by potentially less leaching during set-aside.Spring SMN measurements in the second year after ploughing out the set-aside covers, showed negligible or, for PRG/WC, only slight increases (12 – 18 kg ha^–1) in residual soil N supply after both 3-year and 5-year covers, compared to continuous arable cropping. The extra N mineralisation after cover destruction justified small reductions in fertiliser N inputs for the first, but not second crop following either 3- or 5-year set-aside, unless the cover had contained a large clover content. Both 3-year and 5-year set-aside covers had minimal or no effect on either organic matter content, apart from a slight increase in the PRG/WC treatments, or extractable phosphorus, potassium and magnesium status in the topsoil.     

Measurement of biological dinitrogen fixation in grassland: Comparison of the enriched 15N dilution and the natural 15N abundance methods at different nitrogen application rates and defoliation frequencies

A plant mixture of white clover (Trifolium repens L.), red clover (Trifolium pratense L.), and ryegrass (Lolium perenne L.) was established in the spring of 1991 under a cover-crop of barley. Treatments were two levels of nitrogen (400 and 20 kg N ha^-1) and two cutting intensities (3 and 6 cuts per season). Fixation of atmospheric derived nitrogen was estimated by two ¹⁵N dilution methods, one based on application of ¹⁵N to the soil, the other utilising small differences in natural abundance of ¹⁵N.Both methods showed that application of 400 kg N ha^-1 significantly reduced dinitrogen fixation, while cutting frequency had no effect. Atmospheric derived nitrogen constituted between 50 and 64% of harvested clover nitrogen in the high-N treatment, while between 73% and 96% of the harvested clover nitrogen was derived from the atmosphere in the low-N treatment. The amounts of fixed dinitrogen varied between 31–72 kg N ha^-1 and 118–161 kg N ha^-1 in the high-N and low-N treatment, respectively. The highest values for biological dinitrogen fixation were estimated by the enriched ¹⁵N dilution method.Estimates of transfer of atmospheric derived nitrogen from clover to grass obtained by the natural ¹⁵N abundance method were consistently higher than those obtained by the enriched ¹⁵N dilution method. Neither mineral nitrogen application nor defoliation frequency affected transfer of atmospheric derived nitrogen from clover to grass.Isotopic fractionation of ¹⁴N and ¹⁵N (B value) was estimated by comparing results for nitrogen fixation obtained by the enriched ¹⁵N dilution and the natural ¹⁵N abundance method, respectively. B was on average +1.20, which was in agreement with a B value determined by growing white clover in a nitrogen free media.     

Source of the soybean N credit in maize production

Nitrogen response trials throughout the United States Corn Belt show that economic optimum rates of N fertilization are usually less for maize (Zea mays L.) following soybean (Glycine max L.) than for maize following maize; however, the cause of this rotation effect is not fully understood. The objective of this study was to investigate the source of the apparent N contribution from soybean to maize (soybean N credit) by comparing soil N mineralization rates in field plots of unfertilized maize that had either nodulated soybean, non-nodulated soybean, or maize as the previous crop. Crop yields, plant N accumulation, soil inorganic N, and net soil mineralization were measured. Both grain yield (6.3 vs. 2.8 Mg ha^–1) and above-ground N accumulation (97 vs. 71 kg ha^–1) were greatly increased when maize followed nodulated soybean compared with maize following maize. A partial benefit to yield and N accumulation was also observed for maize following non-nodulated soybean. Cumulative net soil N mineralization following nodulated soybean, non-nodulated soybean, and maize was 112, 92 and 79 kg N ha^–1, respectively. Net mineralization of soil N appeared to be influenced by both quality (C:N ratio) and quantity of residue from the previous crop. In addition to an increase in plant available N from mineralization, the amount of soil inorganic N (especially in soil 5 cm from the row) was greater following nodulated soybean than non-nodulated soybean or maize. Based on these data, the soybean N credit appears to result from a combination of a decrease in net soil mineralization in continuous maize production and an increase in residual soil N from symbiotic fixation.     

Soil nitrogen mineralization in plantations ofJuglans nigra interplanted with actinorhizalElaeagnus umbellata orAlnus glutinosa

Nitrogen mineralization rates were estimated in 19-year-old interplantings of black walnut (Juglans nigra L.) with dinitrogen fixing autumn-olive (Elaeagnus umbellata Thunb.) or black alder (Alnus glutinosa L. Gaertn.) and in pure walnut plantings at two locations in Illinois USA. N mineralization rates were measured repeatedly over a one year period usingin situ incubations of soil cores in oxygen-permeable polyethylene bags at 0–10 and 10–20 cm soil depths, and also by burying mixed-bed ion-exchange resin in soil. Mineralization rates were highest in summer and in plots containing actinorhizal Elaeagnus and Alnus in contrast with pure walnut plots. Elaeagnus plots at one location yielded 236 kg of mineral N ha^–1 yr^–1 in the upper 20 cm of soil, a value higher than previously reported for temperate decidous forest soils in North America. The highest mean plot values for N mineralization in soil at a location were 185 kg ha^–1 yr^–1 for Alnus interplantings and 90 kg ha^–1 yr^–1 for pure walnut plots. Plots which had high N mineralization rates also had the largest walnut trees. Despite low pH (4.1 and 6.5) and low extractable P concentrations (1.4 and 0.7 mg kg^–1 dry mass) at the two locations, nitrification occurred in all plots throughout the growing season. NO ₃ ^– –N was the major form of mineralized N in soil in the actinorhizal interplantings, with NH ₄ ⁺ –N being the major form of mineral N in control plots. Walnut size was highly correlated with soil nitrogen mineralization, particularly soil NO ₃ ^– –N production in a plot.     

The effect of a single application of cow urine on annual N2 fixation under varying simulated grazing intensity, as measured by four 15N isotope techniques

The effects of dairy cow urine and defoliation severity on biological nitrogen fixation and pasture production of a mixed ryegrass-white clover sward were investigated over 12 months using mowing for defoliation. A single application of urine (equivalent to 746 kg N ha^–1), was applied in late spring to plots immediately after light and moderately-severe defoliation (35 mm and 85 mm cutting heights, respectively) treatments were imposed. Estimates of percentage clover N derived from N₂ fixation (%Ndfa) were compared by labelling the soil with ¹⁵N either by applying a low rate of ¹⁵N-labelled ammonium sulphate, immobilising ¹⁵N in soil organic matter, adding ¹⁵N to applied urine, or by utilising the small differences in natural abundance of ¹⁵N in soil. Urine application increased annual grass production by 85%, but had little effect on annual clover production. However, urine caused a marked decline in %Ndfa (using an average of all ¹⁵N methods) from 84% to a low of 22% by 108 days, with recovery to control levels taking almost a year. As a result, total N fixed (in above ground clover herbage) was reduced from 232 to 145 kg N ha^–1 yr^–1. Moderately–severe defoliation had no immediate effect on N₂ fixation, but after 108 days the %Ndfa was consistently higher than light defoliation during summer and autumn, and increased by up to 18%, coinciding with an increase in growth of weeds and summer-grass species. Annual N₂ fixation was 218 kg N ha^–1 yr^–1 under moderately-severe defoliation compared to 160 kg N ha^–1 yr^–1 under light defoliation. Estimates of %Ndfa were generally similar when ¹⁵N-labelled or immobilised ¹⁵N were used to label soil regardless of urine and defoliation severity. The natural abundance technique gave highly variable estimates of %Ndfa (–56 to 24%) during the first 23 days after urine application but, thereafter, estimates of %Ndfa were similar to those using ¹⁵N-labelling methods. In contrast, in urine treated plots the use of ¹⁵N-labelled urine gave estimates of %Ndfa that were 20–30% below values calculated using conventional ¹⁵N-labelling during the first 161 days. These differences were probably due to differences in the rooting depth between ryegrass and white clover in conjunction with treatment differences in ¹⁵N distribution with depth. This study shows that urine has a prolonged effect on reducing N₂ fixation in pasture. In addition, defoliation severity is a potential pasture management tool for strategically enhancing N₂ fixation.     

Soil N mineralization and nitrification in relation to nitrogen solution chemistry in a small forested watershed

Spatial variations in soil processes regulating mineral N losses to streams were studied in a small watershed near Toronto, Ontario. Annual net N mineralization in the 0–8 cm soil was measured in adjacent upland and riparian forest stands using in situ soil incubations from April 1985 to 1987. Mean annual rates of soil N mineralization and nitrification were higher in a maple soil (93.8 and 87.0 kg.ha^–1) than in a pine soil (23.3 and 8.2 kg.ha^–1 ). Very low mean rates of mineralization (3.3 kg.ha^–1) and nitrification (3.4 kg.ha^–1) were found in a riparian hemlock stand. Average NO₃-N concentrations in soil solutions were 0.3–1.0 mg.L^–1 in the maple stand and >0.06mg.L^–1 in the pine stand. Concentrations of NO₃–N in shallow ground water and stream water were 3–4× greater in a maple subwatershed than in a pine subwatershed. Rapid N uptake by vegetation was an important mechanism reducing solution losses of NO₃–N in the maple stand. Low rates of nitrification were mainly responsible for negligible NO₃–N solution losses in the pine stand.     

Net mineralization and nitrification rates in a clay soil measured and predicted in permanent grassland from soil temperature and moisture content

Summary Net mineralization of N and net nitrification in field-moist clay soils (Evesham-Kingston series) from arable and grassland sites were measured in laboratory incubation experiments at 4, 10 and 20°C. Three depth fractions to 30 cm were used. Nitrate accumulated at all temperatures except when the soil was very dry (=0.13 cm³ cm^–3). Exchangeable NH₄-ions declined during the first 24 h and thereafter remained low. Net mineralization and net nitrification approximated to zero-order reactions after 24 h, with Q₁₀ values generally <1.6. The effect of temperature on both processes was linear although some results conformed to an Arrhenius-type relationship. The dependence of net mineralization and net nitrification in the field soil on soil temperature (10 cm depth) and moisture (0–15, 15–25, 25–35 cm depths) was modelled using the laboratory incubation data. An annual net mineralization of 350 kg N ha^–1 and net nitrification of 346 kg N ha^–1 were predicted between September 1980 and August 1981. The model probably overstressed the effect of soil moisture relative to soil temperature.     

Prediction of the non-fertilizer N supply of mineral grassland soils

Different methods for estimating the non-fertilizer N supply (NFNS) of mineral grassland soils were compared. NFNS was defined as the N uptake on unfertilized plots. The potential mineralization rate (0–12 weeks), macroorganic matter and active microbial biomass (determined by the substrate-induced respiration method; SIR) were correlated positively with NFNS. The difference between the actual soil organic N or microbial N content (determined by the fumigation incubation method) and their contents under equilibrium conditions ( org. N and MB-N), however, gave the best estimations of NFNS. For field conditions the best estimation for NFNS was: NFNS (kg N ha^–1 yr^–1)=132.3+42.1× org. N (g kg^–1 soil; r=0.80). This method is based on the observation that, under old grassland swards, close relationships exist between soil texture and the amounts of soil organic N and microbial N. These relationships are assumed to represent equilibrium conditions as under old swards under constant management, the gain in soil organic N and microbial N equals the losses. Soils under young grassland and recently reclaimed soils contained less soil organic N and microbial N. In such soils the amounts of organic N and microbial N increase with time, which is reflected in a lower NFNS. The annual accumulation of organic and microbial N gradually becomes smaller until organic N, microbial N and NFNS reach equilibrium. The main advantage of the difference method in comparison with the other methods is its speed and simplicity.FAX no: +31 50337291     

Denitrification in the top and sub soil of grassland on peat soils

Denitrification is an important process in the nitrogen (N) balance of intensively managed grassland, especially on poorly drained peat soils. Aim of this study was to quantify the N loss through denitrification in the top and sub soil of grassland on peat soils. Sampling took place at 2 sites with both control (0 N) and N fertilised (+ N) treatments. Main difference between the sites was the ground water level. Denitrification was measured on a weekly basis for 2 years with a soil core incubation technique using acetylene (C₂H₂) inhibition. Soil cores were taken from the top soil (0–20 cm depth) and the sub soil (20–40 cm depth) and incubated in containers for 24 hours. The denitrification rate was calculated from the nitrous oxide production between 4 and 24 hours of incubation. Denitrification capacities of the soils and the soil layers were also determined.The top soil was the major layer for denitrification with losses ranging from 9 to 26 kg N ha^–1 yr^–1 from the O N treatment. Losses from the top soil of the + N treatment ranged from 13 to 49 kg N ha^–1 yr^–1. The sub soil contributed, on average, 20% of the total denitrification losses from the 0–40 layer. Losses from the 0–40 cm layer were 2 times higher on the + N treatment than on the O N treatment and totalled up to 70 kg N ha^–1 yr^–1. Significant correlation coefficients were found between denitrification activity on the one hand, and ground water level, water filled pore space and nitrate content on the other, in the top soil but not in the sub soil. The denitrification capacity experiment showed that the availability of easily decomposable organic carbon was an important limiting factor for the denitrification activity in the sub soil of these peat soils.     

Nitrogen inputs and losses from New Zealand dairy farmlets, as affected by nitrogen fertilizer application: year one

Inputs and losses of nitrogen (N) were determined in dairy cow farmlets receiving 0, 225 or 360 kg N ha^-1 (in split applications as urea) in the first year of a large grazing experiment near Hamilton, New Zealand. Cows grazed perennial ryegrass/white clover pastures all year round on a free-draining soil. N₂ fixation was estimated (using ¹⁵N dilution) to be 212, 165 and 74 kg N ha^-1 yr^-1 in the 0, 225 and 360 N treatments, respectively. The intermediate N rate had little effect on clover growth during spring but favoured more total pasture cover in summer and autumn, thereby reducing overgrazing and resulting in 140% more clover growth during the latter period.Removal of N in milk was 76,89 and 92 kg N ha^-1 in the 0, 225 and 360 N treatments, respectively. Denitrification losses were low (7–14 kg N ha^-1 yr^-1), increased with N application, and occurred predominantly during winter. Ammonia volatilization was estimated by micrometeorological mass balance at 15, 45 and 63 kg N ha^-1 yr^-1 in the 0, 225 and 360 N treatments, respectively. Most of the increase in ammonia loss was attributed to direct loss after application of the urea fertilizer.Leaching of nitrate was estimated (using ceramic cup samplers at 1 m soil depth, in conjunction with lysimeters) to be 13, 18 and 31 kg N ha^-1 yr^-1 in a year of relatively low rainfall (990 mm yr^-1) and drainage (170–210 mm yr^-1). Drainage was lower in the N fertilized treatments and this was attributed to enhanced evapotranspiration associated with increased grass growth.Nitrate-N concentrations in leachates increased gradually over time to 30 mg L^-1 in the 360 N treatment whereas there was little temporal variation evident in the 0 (mean 6.4 mg L^-1) and 225 (mean 10.1 mg L^-1) N treatments. Thus, the 360 N treatment had a major effect by greatly reducing N₂ fixation and increasing N losses, whereas the 225 N treatment had little effect on N₂ fixation or on nitrate leaching. However, these results refer to the first year of the experiment and further measurements over time will determine the longer-term effects of these treatments on N inputs, transformations and losses.     

Effects of stubble and N fertilization management on N availability and uptake under successive rice (Oryza sativa L.) crops

Experiments were conducted in fields which had a history of nil to four rice (Oryza sativa L.) crops during the previous four summers. Incorporating stubble after each harvest reduced soil nitrate-N content between crops, but increased soil N mineralization potential. During the fourth successive crop, plots where stubble had been incorporated after the previous three harvests had an average 21% more soil NH₄N and 22% more N uptake than plots where stubble had been burnt.Soil fertility fell rapidly with increasing numbers of crops, and the unfertilized fifth crop accumulated approximately half the N (60 kg N ha^-1) found in the unfertilized first crop (116 kg). Fertilizer N alleviated the effects of annual cropping; the application of 210 kg N ha^-1 to the fifth crop (uptake of 156 kg N ha^-1) resulted in similar N uptake to the first crop fertilized with 50 kg N ha^-1 (154 kg N ha^-1).Applying N at sowing had no significant effect on soil NH₄-N concentration after permanent flood (PF), while N application at PF resulted in increased NH₄-N concentration and N uptake until panicle initiation (PI). N applied at PI increased soil NH₄-N concentration at least until the microspore stage.Management factors such as stubble incorporation and increasing N application rate, maintained N supply and enabled successive rice crops to accumulate similar quantities of N at maturity.     

Fertilizer nitrogen budgets of two doses of Na15NO3 dressings split-applied to winter wheat in microplots on a loam soil

In a field experiment performed in microplots, winter wheat was fertilized at two different total N dressings (135 and 180 kg ha^–1) split-applied as Na¹⁵NO₃ in three equal applications at tillering, stem elongation, and flag leaf.No significant differences were found in the percentage recovery values for the entire plant at the three split applications between the two N dressings. The total percentage recovery of fertilizer N by the plant was high and practically equal at both fertilization levels (76.65% and 75.84% for 135 and 180 kg N ha^–1, respectively); crop yields were also similar. In contrast, gaseous losses calculated after drawing up the balance sheet were, in absolute values, higher for the tillering and stem elongation split applications when using the 180 kg N ha^–1 dressing (7.67 and 4.84 kg N ha^–1, respectively) than for the 135 kg N ha^–1 dressing (3.45 and 1.26 kg N ha^–1, respectively). They were found to be zero at flag leaf at both fertilization levels. The amount of applied fertilizer N did not influence the amount of N taken up from the soil which was about 143 kg ha^–1.     

Effects of nitrogen on leaves,dry matter allocation and regrowth dynamics in Trifolium repens L. and Lolium perenne L. in pure and mixed swards

The effects of applied nitrogen (N) on dynamics of regrowth, dry matter (DM) allocation and leaf characteristics of grass and clover were investigated. Binary mixtures and monocultures of the diploid perennial ryegrass cultivars Barlet (erect) and Heraut (prostrate) and the white clovers cvs. Alice (large-leaved) and Gwenda (small-leaved) were established in a field experiment. Grass monocultures received three levels of N application (0, 140 or 280 kg N ha^–1), and mixtures 150 kg N ha^–1 (+N) or no N (–N). N was applied split over the season. Application of N reduced the average clover content in the DM of the mixtures from 43 to 12%. Due to defoliation, clover lost relatively more leaf area and less DM than grass, leading to a lower clover fraction in the leaf area index (LAI) of the stubble at the start of the next regrowth. In the –N mixtures, the clover fraction of the biomass and of the LAI increased within successive regrowth periods. In the +N mixtures, large-leaved Alice maintained its content during summer, mainly due to its greater petiole length which increased in response to N. The opposite was observed for Gwenda. At each harvest, the content of small-leaved Gwenda in the LAI and DM was lower than in the stubble at the start of regrowth. The allocation of DM to the petioles of Alice led to a decrease in the leaf weight ratio (LWR) in the +N mixtures, while Gwenda had a higher LWR and specific leaf area (SLA) in the +N mixtures than in the –N mixtures. There was little or no effect of ryegrass cultivar on competition with white clover.