Nitrogen mineralisation potential in calcareous soils amended with sewage sludge

Mineralisation of organic N is an important consideration when determining the annual amount of sewage sludge to be applied to agricultural soils. The mineralisation of sludge organic N was studied in two different textured soils (clayey and sandy soil) treated with aerobic and anaerobic sludge at two different rates (30 and 50 g sludge kg(-1) soil). The mineralisation of sludge organic N was determined during 20 weeks incubation period by analysis of inorganic N produced by a non-leached procedure. Sludge organic N mineralisation was influenced by soil type, organic N mineralisation being greater in the sandy soil (from 30% to 41%) than in the clayey soil (from 13% to 24%). Mineralisation rates decreased rapidly the first two weeks, followed by a slower decrease with time. Although total mineralisation increased with sludge addition rate, net mineralisation decreased with sludge addition rate, probably due to denitrificaton losses. The aerobically treated sludge gave higher mineralisation rates than the anaerobically treated one. The values of N0 and k for treated soils varied depending on the type of sludge and soil.     

Mineralisation of nitrogen from an incorporated catch crop at low temperatures: experiment and simulation

The release of nitrogen from incorporated catch crop material in winter is strongly influenced by soil temperatures. A laboratory experiment was carried out to investigate this influence in the range of 1-15 °C. Samples of sandy soil or a mixture of sandy soil with rye shoots were incubated at 1-5-10-15 °C, and samples of sandy soil with rye roots were incubated at 5-10-15 °C. Concentrations of N_min (NH₄ ⁺-N and NO₃ ^--N) were measured after 0-1-2-4-7-10 weeks for the sandy soil and the sandy soil:rye shoot mixture, and after 0-2-7-10 weeks for the sandy soil:rye root mixture. At 1 °C, 20% of total organic N in the crop material had been mineralised after ten weeks, indicating that mineralisation at low temperatures is not negligible. Maximum mineralisation occurred at 15 °C; after ten weeks, it was 39% of total applied organic nitrogen from shoot and 35% from root material. The time course of mineralisation was calculated using an exponential decay function. It was found that the influence of temperature in the range 1-15 °C could be described by the Arrhenius equation, stating a linear increase of ln(k) with T^-1, k being the relative mineralisation rate in day^-1 and T the temperature (°C). A simulation model was developed in which decomposition, mineralisation and nitrification were modelled as one step processes, following first order kinetics. The relative decomposition rate was influenced by soil temperature and soil moisture content, and the mineralisation of N was calculated from the decomposition of C, the C to N ratio of the catch crop material and the C to N ratio of the microbial biomass. The model was validated first with the results of the experiment. The model was further validated with the results of an independent field experiment, with temperatures fluctuating between 3 and 20 °C. The simulated time course of mineralisation differed significantly from the experimental values, due to an underestimation of the mineralisation during the first weeks of incubation.     

Influence of biochemical quality on C and N mineralisation from a broad variety of plant materials in soil

We studied C and N mineralisation patterns from a large number of plant materials (76 samples, covering 37 species and several plant parts), and quantified how these patterns related to biological origin and selected indicators of chemical composition. We determined C and N contents of whole plant material, in water soluble material and in fractions (neutral detergent soluble material, cellulose, hemicellulose and lignin) obtained by stepwise chemical digestion (modified van Soest method). Plant materials were incubated in a sandy soil under standardised conditions (15 °C, optimal water content, no N limitation) for 217days, and CO₂ evolution and soil mineral N contents were monitored regularly. The chemical composition of the plant materials was very diverse, as indicated by total N ranging from 2 to 59 mg N g^–1, (i.e. C/N-ratios between 7 and 227). Few materials were lignified (median lignin=4% of total C). A large proportion of plant N was found in the neutral detergent soluble (NDS) fraction (average 84%) but less of the plant C (average 46%). Over the entire incubation period, holocellulose C content was the single factor that best explained the variability of C mineralisation (r=–0.73 to –0.82). Overall, lignin C explained only a small proportion of the variability in C mineralisation (r=–0.44 to –0.51), but the higher the lignin content, the narrower the range of cumulative C mineralisation. Initial net N mineralisation rate was most closely correlated (r=0.76) to water soluble N content of the plant materials, but from Day 22, net N mineralisation was most closely correlated to total plant N and NDS-N contents (r varied between 0.90 and 0.94). The NDS-N content could thus be used to roughly categorise the net N mineralisation patterns into (i) sustained net N immobilisation for several months; (ii) initial net N immobilisation, followed by some re-mineralisation; and (iii) initially rapid and substantial net N mineralisation. Contrary to other studies, we did not find plant residue C/N or lignin/N-ratio to be closely correlated to decomposition and N mineralisation.     

Seasonal dynamics of denitrification activity in two water meadows

Seasonal variation in denitrification activity was measured in twoflooded water meadows, one on peaty and one on sandy soil, over a three-yearperiod. Measurements were taken during flooded and drained periods, usingthe acetylene-blockage technique, and the rates were compared to massbalance estimates of nitrate removal in the percolating water.Denitrification activity was higher in sandy soil than in peaty soil. Higherwater infiltration rate and thereby higher nitrate load was considered to bethe cause of the higher denitrification in the sandy soil. Floodingsignificantly increased denitrification, and the rates were higher in autumnand winter than in spring. This was considered to be a result of highernitrogen concentration in inflowing stream water during winter. Annualdenitrification was estimated to 430–460 kg N ha^-1yr^-1 in the sandy soil meadow, and 220 kg N ha^-1yr^-1 in the peaty soil meadow. In the sandy soil there was alarge discrepancy between nitrate removal rates and denitrification rates,which can be explained by nitrification of ammonium released from the soil.In the peaty soil nitrate disappearance and denitrification correspondedfairly well.     

Microbial degradation of geogenic organic C and N in mine spoils

Many mine spoils present at the surface of reclamation sites in the Lower Lusatian mining district are carboniferous substrates, i.e. contain geogenic organic matter. Depending on its susceptibility to microbial degradation, geogenic organic matter might influence the establishment of a carbon requiring microflora in mine spoils. As geogenic organic matter contains substantial amounts of organic nitrogen it is also a potential source for plant available N. The objective of the present study was to quantify C and N mineralisation and microbial biomass in geogenic organic matter present at reclamation sites in Lower Lusatia. We also studied, whether these properties can be influenced by raising the originally low pH to near neutral conditions. In laboratory incubation studies, the rates of CO₂ evolution and net N mineralisation were determined in geogenic organic matter and carboniferous mine spoil with and without addition of lime. At the same time, microbial biomass carbon was estimated. As a reference, soil organic matter originating from the humus layer of a 60-year-old Pinus sylvestris stand was used. As indicated by the initial rates of C mineralisation, geogenic carbon was microbially available but to a lower extent than soil organic carbon. During incubation, C mineralisation remained constant or tended to increase with time, depending on the origin of the sample, while it decreased in soil organic matter. Unlike in soil organic matter, in geogenic organic matter and carboniferous mine spoil, C mineralisation was not consistently promoted by lime addition. Prior to incubation, microbial biomass in geogenic organic matter and carboniferous mine spoil was about 10-fold lower than in soil organic matter and tended to increase with incubation time while it decreased in soil organic matter. Similar to C mineralisation, microbial biomass in geogenic organic matter increased after liming, while it declined in carboniferous mine spoil immediately after lime addition. Rates of net N mineralisation were very low in geogenic organic matter and carboniferous mine spoil regardless of the length of incubation and could not be enhanced by raising the pH. It was concluded, that in mine spoils where accumulation of soil organic matter has not yet occurred, geogenic organic matter can be favourable for the establishment of a heterotrophic microflora. However, in the short term, geogenic matter is no source for plant available N in mine spoils. This revised version was published online in June 2006 with corrections to the Cover Date. This revised version was published online in June 2006 with corrections to the Cover Date. This revised version was published online in June 2006 with corrections to the Cover Date.     

Development of nitrogen mineralisation gradients through surface soil depth and their influence on surface soil pH

Following mixing of the surface soil to about 7.5 cm depth in the field, soil layers (0–2.5, 2.5–5, 5–10 and 10–15 cm) were separately incubated in the laboratory to determine the rate of development of net N mineralisation gradients through surface soil depth under fallow, wheat and subterranean clover plots. Gradients in net N mineralisation were compared with those observed in the field, and their contribution to the observed pH changes was investigated.Heterotrophic activity, and thus net N mineralisation, decreased only slightly with depth immediately after soil mixing. This pattern persisted over time in soil layers sampled from fallow plots. In contrast, within 1 growing season after soil mixing, heterotrophic activity and net N mineralisation decreased significantly with depth in soil sampled from wheat and clover plots. In 0–15 cm soil sampled from under senescing plants, 32–38% of CO₂-C produced and net N mineralised originated from the surface 2.5 cm, while 52–56% originated from the surface 5 cm of soil. This resulted from an increase of pH and organic substrate concentration within the surface 2.5 cm of soil following plant residue return. Limitations of the in situ measurement of net N mineralisation in fallow soil was identified.Laboratory incubation studies showed that since most net N mineralisation occurred within the surface 2.5 cm of soil under senescing plants, nitrification and acidification were also concentrated at this depth. Despite this, compared to fallow soil, high potential acidification rates of 0–2.5 cm soil under senescing plants were not realised in the field due to the exposure to prolonged dry periods and moist-dry cycles. As a consequence, in the field the large magnitude of surface soil pH gradient which resulted from the return of alkaline plant residues was maintained over summer and autumn.     

Transformations of residual 15N in a coniferous forest soil humus layer in northern Vancouver Island,British Columbia

We studied the effect of ¹⁵N labelling duration on the mineralisation and immobilisation of native and applied (residual) N in the humus layer of a Humo-Ferric Podzol. Ammonium sulphate, labelled with ¹⁵N, was applied to 1 m² plots at a rate of 200 kg N ha^–1. Fertiliser application was timed so that when samples were collected they had been labelled with ¹⁵N for 24 hours, 7 months and 31 months. In a 42-day aerobic incubation of the samples, net mineralisation of total and applied N was greatest in the 24-hr treatment followed by those from the 31-month treatment (p<0.05), indicating that immobilised ¹⁵N was more remineralisable in the samples with ¹⁵N labelled for 24 hours. The percentage of applied N found in the total N mineralised (net) ranged from 76.6 to 87.4%, 13.1 to 42.0% and 10.6 to 14.0% in samples from the 24-hr and 7- and 31-month treatments, respectively, showing reduced relative availability of residual N with increased labelling duration. The carbon mineralisation rate had the following order: 7-month > 24-hr > 31-month treatment. Net mineralisation of C and N was poorly correlated with each other (r=-0.02, p=0.89). Anaerobic incubation showed net mineralisation for the 7- and 31-month treatments but net immobilisation for the 24-hr treatment for both total and applied N, suggesting that immobilisation of inorganic N was encouraged when there was a large pool of mineral N in the soil. Both total and applied N in the extractable organic N fraction and in the N flushed after fumigation with chloroform had the following order: 24-hr > 7-month > 31-month treatment. The results confirmed that N fertiliser was being immobilised within hours after application by the humus material through the microbial population and that the immobilised N had a low mineralisation potential after one growing season.     

Simulation of field scale denitrification losses from soils under grass ley and barley

Denitrification losses from soils under barley and grass ley crops were simulated. The model, which includes the major processes determining inputs, transformations and outputs of nitrogen in arable soils, represents a scale compatible with information generally available in agricultural field research. The denitrification part of the model includes a field potential denitrification rate and functions for the effect of soil aeration status, soil temperature and soil nitrate content. Easily metabolizable organic matter is assumed not to limit denitrification. Simulated values were compared with denitrification measurements made during two growing seasons in the barley and grass ley treatments of a field experiment in central Sweden.Calibration revealed that the optimal parameter values describing the effect of soil aeration on denitrification rates were similar for both treatments. The response function derived agreed well with two data sets found in the literature. The potential denitrification rate constant, derived in the simulations, was higher for grass ley than for barley, which was consistent with the differences in overall rates of carbon and nitrogen turnover found between treatments.The simulated mean denitrification rates for the two seasons were within 20% of the mean of the measured values. However, simulated denitrification showed less temporal variability and a less skewed frequency distribution than measured denitrification. Some of the measured denitrification events not explained by the model could have been due to the stimulating effects of soil drying/wetting and freezing/thawing on microbial activity.     

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.     

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.     

An assessment of the contribution of net mineralization to N cycling in grass swards using a field incubation method

Measurements of net mineralization using a field incubation method were made over a full growing season (180 d). Soil cores, taken from cut swards which for many years had been previously grazed by cattle, were placed in jars in the field for successive incubation periods of 14 d. Acetylene was added to the incubation jars to inhibit nitrification in the soil cores and thereby prevent losses of N through denitrification. Net mineralization over 180 d amounted to 415, 321 and 310 kg N ha^–1 under grass/clover, unfertilized grass and grass receiving 420 kg N ha^–1 y^–1, respectively. At the start of the growing season, an index of potentially mineralizable N in the soil was estimated by a chemical extraction method, but this index was <50% of the estimates obtained by field incubation. The amount of N in herbage harvested regularly from the swards also under-estimated the supply of N from the soil, with apparent recoveries of 53, 82 and 74% and total yields of N of 240, 263 and 538 (kg N ha^–1) from grass/clover, unfertilized grass and fertilized grass, respectively. Mineralization rates varied significantly with seasonal soil temperature fluctuations, but the incubation method was apparently less sensitive in relation to changes in soil water content. Rates of N-turnover (as % of total soil N) were highest under grass/clover (9%), but similar under fertilized and unfertilized grass swards (approximately 5%).     

Laboratory and field evaluation of broiler litter nitrogen mineralization

Two studies were conducted for this research. First, a laboratory incubation to quantify broiler litter N mineralization with the following treatments: two soil moisture regimes, constant at 60% water fill pore space (WFPS) and fluctuating (60-30% WFPS), three soil types, Brooksville silty clay loam, Ruston sandy loam from Mississippi, and Catlin silt loam from Illinois. Second, a field incubation study to quantify broiler litter N mineralization using similar soils and litter application rates as the laboratory incubation. Broiler litter was applied at an equivalent rate of 350 kg total N ha(-1) for both studies except for control treatments. Subsamples were taken at different timing for both experiments for NO3-N and NH4-N determinations. In the laboratory experiment, soil moisture regimes had no significant impact on litter-derived inorganic N. Total litter-derived inorganic N across all treatments increased from 23 mg kg(-1) at time 0, to 159 mg kg(-1) at 93 d after litter application. Significant differences were observed among the soil types. Net litter-derived inorganic N was greater for Brooksville followed by Ruston and Catlin soils. For both studies and all soils, NH4-N content decreased while NO3-N content increased indicating a rapid nitrification of the mineralized litter N. Litter mineralization in the field study followed the same trend as the laboratory study but resulted in much lower net inorganic N, presumably due to environmental conditions such as precipitation and temperature, which may have resulted in more denitrification and immobilization of mineralized litter N. Litter-derived inorganic N from the field study was greater for Ruston than Brooksville. Due to no impact by soil moisture regimes, additional studies are warranted in order to develop predictive relationships to quantify broiler litter N availability.     

Inhibition of nitrification in forest soil by monoterpenes

Nitrate production was detected in untreated soil of a Norway spruce (Picea abies L.) stand only after clear-cutting the stand. The aim of this study was to determine whether allelochemical inhibition of nitrification by monoterpenes played any role in inhibiting nitrification in the stand. Therefore, soils from a clear-cut plot and from a forest plot were studied. In the field, monoterpenes (mostly - and -pinenes), measured by soil microair diffusive samplers, were intensively produced in the forest plot, but not in the clear-cut plot. In the laboratory, soil samples taken from the forest plot produced only small amounts of monoterpenes, indicating that monoterpenes were mainly produced by the roots and not to great extent by the soil microbial population. The effect of a mixture of monoterpenes (seven major monoterpenes detected in the field) on net nitrification, net N mineralization and denitrification activities of soil from the clear cut plot, and on carbon mineralization of soils from both the forest and clear-cut plots, was studied in the laboratory. In both aerobic incubation experiments and in soil suspensions with excess NH4-N, nitrification was inhibited by exposure to the vapours of monoterpenes at similar concentrations at which they had been detected in forest plot. This indicates direct inhibition of nitrification by monoterpenes. Exposure to monoterpenes did not affect denitrification. However, it increased respiration activity of both soils. This could also indicate indirect inhibition of nitrification by monoterpenes, due to immobilization of mineral N. Thus it seems that monoterpenes could play a role in inhibiting nitrification in the forest soil.     

Role of soil animals in C and N mineralisation

Addition of single species of soil animals to animal-free microcosms often increases total heterotrophic respiration, but sometimes additions of microarthropods have been reported not to increase or even decrease CO₂ evolution rates. Most studies indicate that addition of soil animals increases net N mineralisation. In a study with F/H layer materials from a spruce stand in central Sweden kept at two temperatures (5 and 15°C) and three moisture levels (15, 30 and 60% of WHC), addition of a mixed fauna of soil arthropods, mainly microarthropods, could not be shown to change the CO₂ evolution rates in comparison with materials where arthropods were absent. However, addition of the arthropods significantly increased net N mineralisation for each of the temperature and moisture combinations. The increase due to the arthropods was dependent on soil temperature but not on soil moisture. Because the total net N mineralisation decreased with decreasing soil moisture, the soil arthropods had a much larger relative effect on net N mineralisation under dry than under moist conditions. It is concluded that soil arthropods are important in maintaining net N mineralisation under dry conditions when the microflora is largely inactive. The microbial/faunal release of mineral N is discussed in relation to the CN of the substrate.     

Nitrogen mineralisation in podzol soils under boreal Scots pine and Norway spruce stands

N mineralisation was investigated in the mor humus layer of a podzol at a forested catchment area of Saarejärve Lake in Eastern Estonia. The investigated areas were pine (Rhodococcumunderstorey) and spruce (Vaccinium understorey) stands, which are permanent sample plots of an integrated monitoring network. The seasonal pattern of net N mineralisation was studied by incubating undisturbed cores of mor humus (0–8 cm) in buried polyethylene bags in situ. Samples were collected and incubated between July 1996 and April 1998. The period of incubation was approximately 1 month, except for wintertime when incubation lasted till thawing of ground (5 months). The amounts of mineral nitrogen formed during monthly incubations in vegetation period vary considerably (0.4–8.7 kg ha^–1). About 70% of the variation of net ammonification could be explained by environmental factors - temperature, initial moisture and pH. Ammonium was the dominant form of mineral nitrogen, which is typical for mor humus. The rate of nitrification was very low, and most of the annual net nitrification occurred during just one or two months (May–June, October) depending on site and year. Measured annual net N mineralisation was 29.2 kg ha^–1 for the spruce stand and 23.6 kg ha^–1 for the pine stand. These measures were found to be in good accordance with other N-fluxes in the ecosystem.     

Grass species and soil type effects on microbial biomass and activity

We evaluated plant versus soil type controls on microbial biomass and activity by comparing microbial biomass C, soil respiration, denitrification potential, potential net N mineralization and nitrification in different soils supporting four grass species, and by growing a group of 10 different grass species on the same soil, in two experiments respectively. In the first experiment, none of the microbial variables showed significant variation with grass species while all variables showed significant variation with soil type, likely due to variation in soil texture. In the second experiment, there were few significant differences in microbial biomass C among the 10 grasses but there were significant relationships between variation in microbial biomass C and potential net N mineralization (negative), soil respiration (positive) and denitrification (positive). There was no relationship between microbial biomass C and either plant yield or plant N concentration. The results suggest that 1) soil type is a more important controller of microbial biomass and activity than grass species, 2) that different grass species can create significant, but small and infrequent, differences in microbial biomass and activity in soil, and 3) that plant-induced variation in microbial biomass and activity is caused by variation in labile C input to soil.     

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.     

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.     

Root-induced nitrogen mineralisation: A theoretical analysis

The possibility is examined that carbon (C) released into the soil from a root could enhance the availability of inorganic nitrogen (N) to plants by stimulating microbial activity. The release of soluble C compounds from roots is assumed to occur by one of two general processes: cortical cell death or exudation from intact cells. On the basis of several assumptions chosen to allow maximal amounts of N mineralisation to be calculated, greater amounts of net N mineralisation are theoretically possible at realistic soil C:N ratios of bacteria are grazed by predators such as protozoa, than if bacteria alone are active. More N is mineralised when the substrate released from the root has a high C:N ratio (as in cell death) than when it is relatively N-rich. The amounts of N that a root might realistically cause to be mineralised are unlikely to account entirely for high nitrate inflow rates that have been measured experimentally. However there are circumstances in which the loss of C from roots is essential if any N is to be mineralised and obtained by plants.     

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.