Crop uptake and leaching of 15N applied in ruminant slurry with selectively labelled faeces and urine fractions

Two animal slurries either labelled with ¹⁵N in the urine or in the faeces fraction, were produced by feeding a sheep with unlabelled and ¹⁵N-labelled hay and collecting faeces and urine separately. The slurries were applied (12 g total N ^-2) to a coarse sand and a sandy loam soil confined in lysimeters and growing spring barley (Hordeum vulgare L). Reference lysimeters without slurry were supplied with¹⁵ NH₄ ¹⁵NO³ corresponding to the inorganic N applied with the slurries (6 g N m^-2). In the second year, all lysimeters received unlabelled mineral fertilizer (6 g N m^-2) and grew spring barley. N harvested in the two crops (grain + straw) and the loss of nitrate by leaching were determined. ¹⁵N in the urine fraction was less available for crop uptake than mineral fertilizer ¹⁵N. The first barley crop on the sandy loam removed 49% of the ¹⁵N applied in mineral fertilizer and 36% of that applied with urine. The availability of fertilizer ¹⁵N (36%) and urine¹⁵ N (32%) differed less on the coarse sand. Of the¹⁵ N added with the faeces fraction, 12–14% was taken up by the barley crop on the two soils. N mineralized from faeces compensated for the reduced availability of urine N providing a similar or higher crop N uptake in manured lysimeters compared with mineral fertilized ones.About half of the total N uptake in the first crop originated from the N applied either as slurry or mineral fertilizer. The remaining N was derived from the soil N pool. Substantially smaller but similar proportions of¹⁵ N from faeces, urine and fertilizer were found in the second crop. The similar recoveries indicated a slow mineralization rate of the residual faeces N since more faeces was left in the soil after the first crop.More N was lost by leaching from manured lysimeters but as a percentage of N applied, losses were similar to those from mineral fertilizer. During the first and second winter, 3–5% and 1–3%, respectively, of the ¹⁵N in slurry and mineral fertilizer was leached as nitrate. Thus slurry N applied in spring just before sowing did not appear to be more prone to loss by nitrate leaching than N given in mineral fertilizer. Slurry N accounted for a higher proportion of the N leached, however, because more N was added in this treatment.     

Components of the nitrogen cycle measured for cropped and grassland soil-plant systems

Summary Inputs and outputs to the N balance of a clay soil catchment (Evesham and Kingston series) under grassland and cereals at Wytham near Oxford were measured over 2 years. Soil mineral N (NH₄+NO₃) was measured to 1 m depth at intervals of 2 to 8 weeks. The frequency distribution of these values was approximately log-normal and the geometric mean was used as an estimate of central tendency. Overall, soil mineral N tended to decrease during the study period, but marked fluctuations were observed in autumn (October–November) and early spring (February–March) in the grassland due to mineralization of soil organic N, and in the arable soil in April–May following the application of N fertilizer to the spring barley and winter wheat.N lost by leaching, including a little surface runoff, was calculated from the NO₃ concentration of the catchment drainage and the volume of drainage. The estimate of N leached using concentrations unweighted for flow rate was only 14 per cent less than that based on flow-weighted concentrations. The differences in the uptake of N by cereals and grass between fields were explicable partly in terms of soil type and partly in terms of the timing and amounts of fertilizer added. The results are discussed in the context of steady-state equilibrium of N in the soil-plant system. However, an N balance could not be struck because N input due to mineralization, and N outputs due to gaseous losses and immobilization of N in the soil and root biomasses, were not measured and could not be accurately estimated.     

Immobilisation, remineralisation and residual effects in subsequent crops of dairy cattle slurry nitrogen compared to mineral fertiliser nitrogen

About 50–60% of dairy cattle slurry nitrogen is ammonium N. Part of the ammonium N in cattle slurry is immobilised due to microbial decomposition of organic matter in the slurry after application to soil. The immobilisation and the remineralisation influence the fertiliser value of slurry N and the amount of organic N that is retained in soil. The immobilisation and the remineralisation of 15 N-labelled dairy cattle slurry NH₄-N were studied through three growing seasons after spring application under temperate conditions. Effects of slurry distribution (mixing, layer incorporation, injection, surface-banding) and extra litter straw in the slurry on the plant utilisation of labelled NH₄-N from slurry were studied and compared to the utilisation of ¹⁵N-labelled mineral fertiliser. The initial immobilisation of slurry N was influenced by the slurry distribution in soil. More N was immobilised when the slurry was mixed with soil. Surface-banding of slurry resulted in significant volatilisation losses and less residual ¹⁵N in soil. Much more N was immobilised after slurry incorporation than after mineral fertiliser application. After 2.5 years the recovery of labelled N in soil (0–25 cm) was 46% for slurry mixed with soil, 42% for injected slurry, 22% for surface-banded slurry and 24% for mineral fertiliser N. The total N uptake in a ryegrass cover crop was 5–10 kg N/ha higher in the autumn after spring-application of cattle slurry (100–120 kg NH₄-N/ha) compared to the mineral fertiliser N reference, but the immobilised slurry N (labelled N) only contributed little to the extra N uptake in the autumn. Even in the second autumn after slurry application there was an extra N uptake in the cover crop (0–10 kg N/ha). The residual effect of the cattle slurry on spring barley N uptake was insignificant in the year after slurry application (equivalent to 3% of total slurry N). Eighteen months after application, 13% of the residual ¹⁵N in soil was found in microbial biomass whether it derived from slurry or mineral fertiliser, but the remineralisation rate (% crop removal of residual ¹⁵N) was higher for fertiliser- than for slurry-derived N, except after surface-banding. Extra litter straw in the slurry had a negligible influence on the residual N effects in the year after application. It is concluded that a significant part of the organic N retained in soil after cattle slurry application is derived from immobilised ammonium N, but already a few months after application immobilised N is stabilised and only slowly released. The immobilised N has negligible influence on the residual N effect of cattle slurry in the first years after slurry application, and mainly contributes to the long-term accumulation of organic N in soil together with part of the organic slurry N. Under humid temperate conditions the residual N effects of the manure can only be optimally utilised when soil is also covered by plants in the autumn, because a significant part of the residual N is released in the autumn, and there is a higher risk of N leaching losses on soils that receive cattle slurry regularly compared to soils receiving only mineral N fertilisers.     

Denitrification and N2O emissions from a UK pasture soil following the early spring application of cattle slurry and mineral fertiliser

Total denitrification and nitrous oxide (N₂O) losses were measured from three contrasting dairy management systems representing good commercial practice (system 1), production maintained but with reduced N losses (system 2); and nitrate leaching less than 50 mg L^-1 but with reduced production (system 3). Measurements were made following mineral fertiliser application and from two plot experiments where four treatments were applied: control, NH₄NO₃ at 60 kg N ha^-1, cattle slurry applied to the surface (equivalent to 45 kg N ha^-1), and cattle slurry injected. Despite low soil temperatures (<6 °C) and low rainfall (<3 mm), total denitrification and N₂O losses peaked at 56 and 16 g N ha^-1 d^-1, respectively. Total denitrification losses decreased: system 1 system 2 > system 3, whereas N₂O losses decreased: system 2 > system 3 > system 1. Total denitrification losses tended to decrease with decreasing fertiliser application rate, whereas fertiliser application rate was not the sole determinant of the N₂O loss. The system 3 field was injected with cattle slurry for 2 yr, system 2 received some slurry by injection and system 1 received slurry to the surface. Thus, the amount, timing and method of previous cattle slurry application was important in determining the loss following subsequent fertiliser application. For the plot experiments, total denitrification and N₂O losses decreased in the order: slurry injected > mineral fertiliser > slurry applied to the surface > control for 5 days following application. However, 16 and 19 days after application, N₂O losses above the control were measured from plots that had received cattle slurry. It was inferred that the application of cattle slurry to the pasture soil stimulated greater N₂O production and increased losses over a longer time period compared with mineral fertiliser additions.     

Soil nitrogen heterogeneity in a Dehesa ecosystem

The C mineralization and N transformations during the decomposition of sunflower stalks (Helianthus annuus L.) and wheat straw (Triticum aestivum L.) with and without addition of (NH₄)₂SO₄ (27.53 atom% ¹⁵N) were studied in a Vertisol. Soil samples were incubated under aerobic conditions for 224 days at 22 °C. The plant residues were added at a rate of 5.2 g kg^-1 soil. Nitrogen was applied at a rate of 50.7 mg N kg^-1 soil. Carbon dioxide emission and inorganic N content in soil were periodically determined. Gross N immobilization and remineralization were calculated on the basis of the isotopic dilution technique. At the end of the incubation period a ¹⁵N balance was established. Respectively, 68 and 45% of the applied residue-C mineralized from the sunflower stalks and wheat straw after 224 days. Both crop residues caused losses of up to 25% of added ¹⁵N after 224 days of incubation. These ¹⁵N losses were about three times larger than in the control soil, and were probably due to denitrification. The net immobilization of soil derived N following residue incorporation was largest in the case of wheat straw, depleting all soil inorganic N. In the wheat straw treatment with added (NH₄)₂SO₄ soil inorganic N remained available, resulting in an enhanced initial C mineralization and N immobilization compared to the treatment without added N. In the case of the sunflower stalks, the high inorganic N content of the stalks suppressed the effects of N addition on C mineralization and N immobilization/mineralization. Gross N immobilization amounted to 31.9 and 28.2 mg N g^-1 added C after 14 days for wheat straw and sunflower stalks, respectively. At the end of the incubation, about 35% of the newly immobilized N was remineralized in both plant residue treatments. Gross N immobilization plotted against decomposed C suggests that fairly uniform C-N relationships exist during the decomposition of divers C substrates. The results demonstrate that low fertilizer N use efficiencies may be expected in a wheat-sunflower cropping system with incorporation of crop residues, as the fertilizer N applied becomes largely immobilized in the soil organic fraction. This revised version was published online in August 2006 with corrections to the Cover Date.     

Denitrification losses from a natural grassland in the Basque Country under organic and inorganic fertilization

Denitrification losses from a poorly drained clayey loamy soil under natural pasture were measured over a two-year period using the acetylene inhibition technique. Plots received two different applications of fertilizer as calcium ammonium nitrate or cow slurry (a total of 145–290 kg N ha^–1 in 1991 and 120–240 kg in 1992). In the first year, N losses in the mineral treatments were about 4 times greater than losses in the slurry treatments. In the second year losses in the slurry treatments increased in such a way that losses in the higher slurry application became similar to those for the two mineral treatments. Soil nitrate was the factor producing differences between treatments. In this way, N mineralization in periods between fertilizations coinciding with high soil water contents was responsible in the second year for the increase in N losses in the slurry treatments. Denitrification rates greater than 0.1 kg N ha^–1 day^–1 occurred at soil water contents > 33 % (air filled porosity < 26 %) and soil nitrate contents > 1 mg N kg^–1 dry soil. Spring and autumn were the seasons of highest risk of denitrification because of N fertilizations coinciding with periods of soil saturation with water. Winter losses were low, but this is a period when there is a risk of denitrification in wetter seasons, particularly for a slurry application management.     

Effects of an organic manure on the transformations of ammonium nitrogen in planted and unplanted soil

Cattle slurry supplemented with ¹⁵N labelled ammonium sulphate was applied to unplanted soil and to soil planted with sprouted potato tubers. For comparison, there was a similar treatment with ¹⁵N labelled ammonium sulphate alone. The pots of soil were kept at 20°C and the plants were harvested after 21, 42, 70 and 98 days. Labelled and unlabelled nitrogen were measured in the plants and, after the same intervals, in the soil as mineral, organic and clay-fixed nitrogen. The recovery of labelled nitrogen in plants plus soil by the end of the experiment was 90% with ammonium sulphate alone and 77% with cattle slurry; the corresponding recoveries in unplanted soil were only 65% and 48%. The greater recoveries of the labelled nitrogen in the planted soil are attributed to its greater protection against gaseous loss when within the plants. Another effect of the plants was to decrease the amount of labelled nitrogen that had been initially fixed by the clay. During the first 21 days with cattle slurry almost half of the labelled nitrogen became immobilized in organic matter. In the same period there was mineralization of unlabelled nitrogen, but the overall reaction was net immobilization. In later periods, immobilized labelled nitrogen in the unplanted soil decreased indicating remineralization. Estimates are given of the rates of gross mineralization, but the periods between sampling occasions were too long to yield reliable values. ei]Section editor: R Merckx     

Mineralization-immobilization and plant uptake of nitrogen as influenced by the spatial distribution of cattle slurry in soils of different texture

The effect of incorporating cattle slurry in soil, either by mixing or by simulated injection into a hollow in soil, on the ryegrass uptake of total N and ¹⁵NH₄ ⁺-N was determined in three soils of different texture. The N accumulation in Italian ryegrass (Lolium multiflorum L.) from slurry N and from an equivalent amount of NH₄ ⁺-N in (¹⁵NH₄) SO₄ (control) was measured during 6 months of growth in pots. After this period the total recovery of labelled N in the top soil plus herbage was similar in the slurry and the control treatments. This indicated that gaseous losses from slurry NH₄ ⁺-N were insignificant. Consequently, the availability of slurry N to plants was mainly influenced by the mineralization-immobilization processes. The apparent utilization of slurry NH₄ ⁺-N mixed into soil was 7%, 14% and 24% lower than the utilization of (NH₄)₂SO₄-N in a sand soil, a sandy loam soil and a loam soil, respectively. Thus, the net immobilization of N due to slurry application increased with increasing soil clay content, whereas the recovery in plants of ¹⁵N-labelled NH₄ ⁺-N from slurry was similar on the three soils. A parallel incubation experiment showed that the immobilization of slurry N occurred within the first week after slurry application. The incorporation of slurry N by simulated injection increased the plant uptake of both total and labelled N compared to mixing the slurry into the soil. The apparent utilization of injected slurry NH₄ ⁺-N was 7% higher, 8% lower and 4% higher than the utilization of (NH₄)₂SO₄-N in the sand, the sandy loam and the loam soil, respectively. It is concluded that the spatial distribution of slurry in soil influenced the net mineralization of N to the same degree as did the soil type.     

Carbon and nitrogen turnover in adjacent grassland and cropland ecosystems

The effects of cultivation and soil texture on net and gross N mineralization, CO₂ evolution and C and N turnover were investigated using paired grassland and cropped sites on soils of three textures. Gross N mineralization and immobilization were measured using¹⁵N-isotope dilution. Grassland soils had high CO₂ evolution and gross N mineralization rates, and low net N mineralization rates. Cropland soils had low CO₂ evolution rates but had high net and gross N mineralization rates. Grassland soils thus had high immobilization rates and cropland soils had low immobilization rates. Cultivation increased N turnover but reduced C turnover. The data suggest that the microflora in grassland soils are N limited, while those of cropland soils are limited by C availability. Increasing clay content reduced N turnover. C turnover was less clearly related to texture. Differences in the immobilization potential of substrates help explain why agricultural soils have higher N losses than do grassland soils.     

The fate of fresh and stored 15N-labelled sheep urine and urea applied to a sandy and a sandy loam soil using different application strategies

The fate of nitrogen from ¹⁵N-labelled sheep urine and urea applied to two soils was studied under field conditions. Labelled and stored urine equivalent to 204 kg N ha^–1 was either incorporated in soil or applied to the soil surface prior to sowing of Italian ryegrass (Lolium multiflorum L.), or it was applied to ryegrass one month after sowing. In a sandy loam soil, 62% of the incorporated urine N and 78% of the incorporated urea N was recovered in three cuts of herbage after 5 months. In a sandy soil, 51–53% of the labelled N was recovered in the herbage and the distribution of labelled N in plant and soil was not significantly different for incorporated urine and urea. Almost all the supplied labelled N was accounted for in soil and herbage in the sandy loam soil, whereas 33–34% of the labelled N was unaccounted for in the sandy soil. When the stored urine was applied to the soil surface, 20–24% less labelled N was recovered in herbage plus soil compared to the treatments where urine or urea were incorporated, irrespective of soil type. After a simulated urination on grass, 69% of the labelled urine N was recovered in herbage and 15% of the labelled N was unaccounted for. The labelled N unaccounted for was probably mainly lost by ammonia volatilization.Significantly more urine- than urea-derived N (36 and 19%, respectively) was immobilized in the sandy loam soil, whereas the immobilization of N from urea and urine was similar in the sandy soil (13–16%). The distribution of urine N, whether incorporated or applied to the soil surface prior to sowing, did not influence the immobilization of labelled urine N in soil. The immobilization of urine-derived N was also similar whether the urine was applied alone or in an animal slurry consisting of labelled urine and unlabelled faecal N. When urine was applied to growing ryegrass at the sandy loam soil, the immobilization of urine-derived N was significantly reduced compared to application prior to sowing. The results indicated that the net mineralization of urine N was similar to that of urea in the sandy soil, but only about 75% of the urine N was net mineralized in the sandy loam soil, when urine was applied prior to sowing. Thus, the fertilizer effect of urine N may be significantly lower than that of urea N on fine-textured soils, even when gaseous losses of urine N are negligible.     

A model to predict transformations and losses of nitrogen in UK pastures grazed by beef cattle

The model simulates the cycling of N in grassland systems grazed by beef cattle and predicts the annual amount of N in liveweight gain, and the amounts lost through ammonia volatilization, denitrification and leaching, on the basis of fertilizer application and soil and site characteristics. It aims to provide a better understanding of the way in which these various factors interact in their influence on N transformations. The model has been programmed to run on IBM-compatible personal computers and responds rapidly to changes in input parameters. The model has been constructed from the average annual amounts of N passing through various components of the N cycle in ten field systems grazed by beef cattle. The amounts were either measured directly or were calculated from empirical sub-models, assuming a balance between inputs to, and outputs from the soil inorganic N pool. The model is given wide applicability through the inclusion of a mineralization sub-model which is sensitive to soil texture, sward age, previous cropping history, and climatic zone. Another important sub-model determines the partitioning of soil inorganic N to either plant uptake or the processes of loss: the proportion partitioned to plant uptake decreases as the total amount of soil inorganic N increases. Outputs from the model indicate that fertilizer N has a strong influence on ammonia volatilization, denitrification and leaching at a given site but that, over a range of sites with a given rate of fertilizer N, total loss and the proportions lost by the three processes are greatly influenced by the amount of N mineralized by the soil. The model indicates how fertilizer N should be matched with mineralization to limit gaseous and leaching losses and to achieve optimum efficiency of N use in grazing systems.     

Effect of straw incorporation on the yield and nitrogen balance in the sandy soil-pearl millet cropping system of Senegal

Summary In a lysimetric experiment conducted in a sandy soil of Senegal, nitrogen fertilization (¹⁵N) and straw incorporation, were combined factorially, the soil being left bare or cropped with millet. On the one hand, yields were estimated, and on the other hand nitrogen absorption, immobilization, and losses were estimated in the soil-plant system. The depressive effect of straw incorporation on grain yield (32% on the average) was attributed mainly to the immobilization of fertilizer nitrogen in the rhizosphere. The depressive effect of such immobilization was alleviated by additional applications of nitrogen. Increasing the quantity of straw incorporated beyond the average amount resulted in a decrease of straw yield but had no effect on grain yield. Straw incorporation was thought to impede the plant growth during early stages but to promote it afterwards. Moreover, when the yield expressed in a fertilizer nitrogen unit basis was the highest, more than half of the plant nitrogen was nevertheless provided by the soil. The authors infer from this fact that soil organic matter was important in the efficiency of nitrogen fertilizer on pearl millet. The reduction of fertilizer nitrogen absorption following straw incorporation and not compensated by additional nitrogen fertilizer storage in the soil appeared to be related (cause or effect) to the increase of total fertilizer losses. Atmospheric losses significantly contributed to total losses (on the average 45%) of the fertilizer nitrogen applied to a planted soil. These losses can be mainly attributed to denitrification.     

Turnover of residual 15N-labelled fertilizer N in soil following harvest of oilseed rape (t Brassica napus L.)

We studied the fate of ¹⁵N-labelled fertilizer nitrogen in a sandy loam soil after harvest of winter oilseed rape (Brassica napus L. cv. Ceres) given 100 or 200 kg N ha^-1 in spring, with or without irrigation. Our main objective was to quantify the temporal variations of the soil mineral N, the extractable soil organic N and soil microbial biomass N, and fertilizer derived N in these pools during autumn and winter. Nitrogen use efficiency of the oilseed rape crop varied from 47% of applied N in the 100N, irrigated treatment to 34% in the 200N, non-irrigated treatment. However, only in the latter treatment did we find significantly higher fertilizer derived soil mineral N than in the three other treatments which all had low soil mineral N contents at the first sampling after harvest (8 days after stubble tillage). Between 31% and 42% of the applied N could not be accounted for in the harvested plants or 0-15 cm soil layer at this first sampling. Over the following autumn and winter none of the remaining fertilizer derived soil N was lost from the 0–5 cm depth, but from the 5–15 cm depth a marked proportion of N derived from fertilizer was lost, probably by leaching. Negligible amounts of fertilizer derived extractable soil organic and mineral N (<1 kg N ha^-1, 0-15 cm) were found in all treatments after the first sampling.Soil microbial biomass N was not significantly affected by treatments and showed only small temporal variability (±11% of the mean 76 kg N ha^-1, 0- 15 cm depth). Surprisingly, the average amount of soil microbial biomass N derived from fertilizer was significantly affected by the treatments, with the extremes being 5.5 and 3.1 kg N ha^-1 in the 200N, non-irrigated and 100N, irrigated treatments, respectively. Also, the estimated exponential decay rate of microbial biomass N derived from fertilizer, differed greatly (2 fold) between these two treatments, indicating highly different microbial turnover rates in spite of the similar total microbial biomass N values. In studies utilising ¹⁵N labelling to estimate turnover rates of different soil organic matter pools this finding is of great importance, because it may question the assumption that turnover rates are not affected by the insertion of the label.     

Tree Patches Show Greater N Losses but Maintain Higher Soil N Availability than Grassland Patches in a Frequently Burned Oak Savanna

Long-term prescribed fires have increased woody canopy openness and reduced nitrogen (N) cycling (that is, net N mineralization) in an oak savanna in Minnesota, USA. It is unclear how fire-induced shifts from oak-dominated to C4 grass-dominated vegetation contribute to this decline in N cycling compared to direct effects of increasing fire frequency promoting greater N losses. We determined (1) the magnitude of decline in net N mineralization in oak versus grass-dominated patches with increasing fire frequency and (2) if differences in net N mineralization between oak and grass patches in frequently burned oak savanna (burned 8 out of 10 years on average during the last 40 years) could be attributed to differences in N losses through volatilization and leaching or to plant traits affecting decomposition and mineralization. In situ net N mineralization declined with increasing fire frequency overall, but this decline was less in oak- than in grass-dominated patches, with oak-dominated patches having more than two times higher net N mineralization than grass-dominated patches. Greater net N mineralization in oak-dominated patches occurred despite greater N losses through volatilization and leaching (on average 1.8 and 1.4 g m⁻² y⁻¹ for oak- and grass-dominated patches, respectively), likely because of higher plant litter N concentration in the oak-dominated patches. As total soil N pools in the first 15 cm did not differ between oak- and grass-dominated patches (on average 83 g N m⁻²), N inputs from atmospheric deposition and uptake from deep soil layers may offset higher N losses. Our results further show that net N mineralization rates decline within 5 years after tree death and subsequent colonization by C4 grasses to levels observed in grass-dominated patches. Although long-term prescribed fires often directly reduce N stocks and cycling because of increased N losses, this study has shown that fire-induced shifts in vegetation composition can strongly contribute to the declines in N cycling in systems that are frequently disturbed by fires with potential feedbacks to plant productivity.     

Long-term nitrogen fertilizer replacement value of cattle manures applied to cut grassland

Manures supply nitrogen (N) to crops beyond the year of application. This N must be taken into account for agronomic and environmental reasons. From 2002 to 2006 we conducted a field experiment on a sandy soil in The Netherlands (52°03″N, 6°18″E) to better quantify this residual N effect. Treatments comprised different time series of mineral fertilizer N or cattle manures of different compositions, all applied at a rate of 300 kg total N ha⁻¹ year⁻¹, whilst compensating for differences in available potassium and phosphorus. Dry matter and N yields of cut grassland responded positively (P < 0.05) to both current manure applications and applications in previous years, whereas mineral fertilizer N affected yields in the year of application only. N yields could be reasonably well predicted with a simple N model, adopting an annual relative decomposition rate of the organic N in manure of 0.10–0.33 year⁻¹ during the year of application and 0.10 year⁻¹ in the following years. Subsequent model calculations indicated that the N fertilizer value (NFRV) of injected undigested cattle slurry rises from an observed 51–53% when slurry is applied for the first time, to approximately 70% after 7–10 yearly applications, whereas it took two to four decades of yearly applications to raise the NFRV of surface applied farm yard manure to a similar level from an initial value of 31%. Manures with a relatively high first year NFRV (e.g. anaerobically digested slurry) had a relatively small residual N effect, whereas manures with a low first year NFRV (e.g. farm yard manure) partly compensated for this by showing larger residual effects. Given the long manuring history of most agricultural systems, rethinking the fertilizer value of manure seems justified. The results also imply that the long term consequences of reduced N application rates may be underestimated if manuring histories are insufficiently taken into account.     

Effects of elevated CO2, temperature and N fertilization on nitrogen fluxes in a temperate grassland ecosystem

The soil nitrogen cycle was investigated in a pre‐established Lolium perenne sward on a loamy soil and exposed to ambient and elevated atmospheric CO₂ concentrations (350 and 700 μL L^?1) and, at elevated [CO₂], to a 3 °C temperature increase. At two levels of mineral nitrogen supply, N– (150 kgN ha^?1 y^?1) and N+ (533 kgN ha^?1 y^?1), ¹⁵N‐labelled ammonium nitrate was supplied in split applications over a 2.5‐y period. The recovery of the labelled fertilizer N was measured in the harvests, in the stubble and roots, in the macro‐organic matter fractions above 200 μm in size (MOM) and in the aggregated organic matter below 200 μM (AOM). Elevated [CO₂] reduced the total amount of N harvested in the clipped parts of the sward. The harvested N derived from soil was reduced to a greater extent than that derived from fertilizer. At both N supplies, elevated [CO₂] modified the allocation of the fertilizer N in the sward, in favour of the stubble and roots and significantly increased the recovery of fertilizer N in the soil macro‐organic matter fractions. The increase of fertilizer N immobilization in the MOM was associated with a decline of fertilizer N uptake by the grass sward, which supported the hypothesis of a negative feedback of elevated [CO₂] on the sward N yield and uptake. Similar and even more pronounced effects were observed for the native N mineralized in the soil. At N–, a greater part of the fertilizer N organized in the root phytomass resulted in an underestimation of N immobilized in dead roots and, in turn, an underestimation of N immobilization in the MOM. The 3 °C temperature increase alleviated the [CO₂] effect throughout much of the N cycle, increasing soil N mineralization, N derived from soil in the harvests, and the partitioning of the assimilated fertilizer N to shoots. In conclusion, at ambient temperature, the N cycle was slowed down under elevated [CO₂], which restricted the increase in the aboveground production of the grass sward, and apparently contributed to the sequestration of carbon belowground. In contrast, a temperature increase under elevated [CO₂] stimulated the soil nitrogen cycle, improved the N nutrition of the sward and restricted the magnitude of the soil C sequestration.     

The use of mean pool abundances to interpret 15N tracer experiments

A pulse dilution ¹⁵N technique was used in the field to determine the effect of the ammonium to nitrate ratio in a fertilizer application on the uptake of ammonium and nitrate by ryegrass and on gross rates of mineralization and nitrification. Two experiments were performed, corresponding approximately to the first and second cuts of grass. Where no substantial recent immobilization of inorganic nitrogen had occurred, mineralization was insensitive to the form of nitrogen applied, ranging from 2.1–2.6 kg N ha^-1 d^-1. The immobilization of ammonium increased as the proportion of ammonium in the application increased. In the second experiment there was evidence that high rates of immobilization in the first experiment were associated with high rates of mineralization in the second. The implication was that some nitrogen immobilized in the first experiment was re-mineralized during the second. Whether this was nitrogen taken up, stored in roots and released following defoliation was not clear. Nitrification rates in this soil were low (0.1–0.63 kg N ha^-1 d^-1), and as a result, varying the ratio of ammonium to nitrate applied markedly altered the relative uptake of ammonium and nitrate. In the first experiment, where temperatures were low, preferential uptake of ammonium occurred, but where >90% of the uptake was as ammonium, a reduction in yield and nitrogen uptake was observed. In the second experiment, where temperatures and growth rates were higher, the proportion of ammonium to nitrate taken up had no effect on yield or nitrogen uptake.     

The fate of labelled15N urea and ammonium nitrate applied to a winter wheat crop

Labelled urea or ammonium nitrate was applied to winter wheat growing on a loamy soil in Northern France. Two applications of fertilizer were given: 50 kg N ha^–1 at tillering (early March) and 110 kg N ha^–1 at the beginning of stem elongation (mid-April). The kinetics of urea hydrolysis, nitrification of ammonium and the disappearance of inorganic nitrogen were followed at frequent intervals. Inorganic nitrogen soon disappeared, mainly immobilized by soil microflora and absorbed by the crop. Net immobilization of fertilizer N occured at a very similar rate for urea and ammonium nitrate. Maximum immobilization (16 kg N ha¹) was found at harvest for the first dressing and at anthesis for the second dressing (23 kg N ha¹). During the nitrification period, the labelled ammonium pool was immobilized two to three times faster than the labelled nitrate pool. No significant net¹⁵N remineralization was found during the growth cycle.The actual denitrification and volatilization losses were probably more important than indicated from calculations made by extrapolation of fluxes measured over short intervals. However microbial immobilization was the most important of the processes which compete with plant uptake for nitrogen.     

Cumulative effects of catch crops on nitrogen uptake, leaching and net mineralization

Catch crops can effectively decrease nitrate leaching in arable cropping systems but their long-term impacts on nitrogen mineralization are not well known. This study quantified the effects of continuous catch crops on net N mineralization, crop N uptake, crop N use efficiency and N leaching in three long-term (13?C17?years) field experiments in northern France. Mustard was grown every year at Boigneville, radish every year at Thibie and ryegrass every 2?years at Kerlavic. The mean N content of catch crop residues at these sites was 33, 36 and 35?kg ha^?1 yr^?1 and their mean C:N ratio was 13, 17 and 28, respectively. Net mineralization was calculated with a mass balance of soil mineral N using measured inputs and outputs. Catch crop establishment enhanced annual mineralization by on average 26, 18 and 9?kg N ha^?1 yr^?1 respectively during the 13?C17?year period. The difference in mineralization rate between catch crop and control treatments (extra mineralization) was positive from the first year at Boigneville, whereas it was negative or nil during the first 3?C5?years at Thibie and Kerlavic. At the latter sites, the extra mineralization rate increased significantly over time at a rate of 2.0 and 2.6?kg N ha^?1 yr^?2. At the end of the experiment, cumulative extra mineralization represented 72%, 60% and 23% of the total N added by catch crop residues at Boigneville, Thibie and Kerlavic, respectively. Repeated catch crops significantly increased N uptake and N use efficiency by main crops at Kerlavic and Thibie, but not at Boigneville. The efficiency of catch crops in reducing N leaching persisted over the years at all sites. A model simulating C and N dynamics during catch crop decomposition was able to reproduce the pattern of extra N mineralization kinetics with the various catch crop species, but underestimated the range of variation between sites. Better predictions were obtained when C or N inputs due to catch crops were increased by 10?C57%, suggesting that the actual inputs could be markedly greater than those measured in catch crop residues. According to the model, the C:N ratio of catch crop residues largely explained differences in mineralization due to different catch crop species.     

Inmobilization-remineralization of NO3-N and total N balance during the decomposition of glucose,sucrose and cellulose in soil incubated at different moisture regimes

A laboratory incubation experiment was conducted to study the effect of organic amendment and moisture regimes on the immobilization-remineralization of NO₃-N and total N balance in soil fertilized with KNO₃. Immobilization of NO₃-N was very rapid in soil amended with glucose and sucrose followed by a remineralization of organic N and accumulation of mineral N. Cellulose caused a slow but continued immobilization and did not show net accumulation of mineral N during 8 weeks of incubation. At the end of incubation, a significant increase in total N and organic N content of the soil was observed which is perhaps attributable to the activity of free living N₂ fixers. Although N losses seemed to have occurred at 100% WHC through denitrification in soil amended with glucose and sucrose, main cause of NO₃ elimination was microbial immobilization.