Nitrogen balance in the Trachypogon grasslands of Central Venezuela

The nitrogen balance of a Trachypogon grassland in Calabozo, Venezuela, is calculated for average conditions using biomass accumulation, nitrogen content, and turnover rates of organic matter. Burning Trachypogon grasslands results in losses of 8.5 kg N ha^?1 yr^?1, while rainfall inputs average 2.6 kg N ha^?1 yr^?1. Uptake of N by vegetation is 14.8 kg N ha^?1 yr^?1, but the total N required to build new tissue during a growing season is about 30 kg N ha^?1 yr^?1, so that about 50% of the nitrogen in the vegetation is recycled internally. Nitrogen lossesvia fire are probably balanced by biological N₂-fixation, but no data are available for N-fixation in these savannas. The calculations presented in this paper are based on few data and more measurements are needed to develop a conclusive picture of the N-balance of Trachypogon grasslands.     

Nitrogen fixation in a Mexican coffee plantation

Fertilizer studies in Mexico indicate that coffee production can be stimulated by added nitrogen. One traditional method of coffee cultivation employs leguminous trees for shade, but these species may also play an important role in coffee production by biologically fixing nitrogen. The presence and importance of nitrogen fixation was evaluated in four systems: coffee only, coffee plus the leguminous shade treeInga jinicuil Schletchter, coffee plus the leguminous treeInga vera H.B. and K., and coffee plus banana and orange trees. In all systems coffee leaves with epiphylls, wood litter, soil, roots, and root nodules were assayed for nitrogen fixing activity with the acetylene reduction technique. All components of these systems exhibited activity except roots. Total apparent fixation was highest in theInga jinicuil site, and equivalent to >40 kg N ha^?1 yr^?1 assuming a 3∶1 C₂H₂∶N₂ ratio. The activity was primarily associated withInga jinicuil nodules. Apparent fixation in the other three sites was less than 1 kg N ha^?1 yr^?1. Nitrogen fixed in theI. jinicuil site was 53% of the average amount of fertilizer nitrogen applied annually, suggesting that fixation by non-crop legumes can be an important nitrogen source for coffee agro-ecosystems.     

Nitrogen Depletion and Redistribution by Free‐Ranging Cattle in the Restoration Process of Mosaic Landscapes: The Role of Foraging Strategy and Habitat Proportion

In a mosaic landscape in N‐Belgium (W‐Europe), consisting of forest, grassland, and wooded pasture on former agricultural land, we assessed nitrogen redistribution by free‐ranging cattle (±0.2 animal units ha^?1 yr^?1). We examined if the spatial redistribution of nitrogen among habitats by cattle could restore nutrient‐poor conditions in preferred foraging habitats, and conversely whether such translocation could lead to extreme eutrophication in preferred resting habitats. We used nitrogen content of different diet classes, habitat use, foraging and defecation behavior, weight gain, and nitrogen losses in the actual situation to explore four different habitat proportion scenarios and two different foraging strategies to calculate a net nitrogen balance per habitat. An atmospheric deposition of 30 kg N ha^?1 yr^?1 with varying interception factors according to the habitat types was included in an integrated nitrogen balance. All scenarios showed a net nitrogen transport from grassland and wooded pasture to forest habitat. We found that nitrogen redistribution strongly depends on habitat proportion. Nitrogen losses from preferred grassland habitat can be high, given its proportion is small. Depletion is only to be expected at excretion‐free areas and probably is of minor importance to trigger the establishment of woody species. In general, nitrogen transported by cattle was much lower than input by atmospheric deposition, but grazing can compensate for high N inputs in excretion‐free areas and maintain grassland types that support critical loads of 20–25 kg N ha^?1 yr^?1. In none of the scenarios, N transport by cattle resulted in the exceeding of critical nitrogen loads to vulnerable forest ground vegetation.     

Nitrogen cycle of tropical perennial crops under shade trees

The distribution and fluxes of nitrogen in some parts of a coffee plantation under shade were studied at a typical mountain (1380 m a sl) location in Venezuela. The amounts of nitrogen in the soil to 60 cm depth are by far the largest nitrogen store, reaching a total of 49 000 kg ha^?1. The nitrogen flow associated with litterfall was dominated by the shade-tree fraction accounting for a transfer of 86 kg ha^?1 yr^?1 of the total 189 kg ha^?1 yr^?1. The rapid decomposition of this litter, although showing a phase of nitrogen accumulation, is an important source of nitrogen to the roots of coffee which occupy preferentially the upper 30 cm of soil and even the litter layer itself. Some evidence of synchrony was found between the peaks of nitrogen transfer to the soil by litter and the periods of high nitrogen demand by the crop plants. It is proposed that the system can amply compensate the nitrogen outputs by harvest (17 kg ha^?1 yr^?1) with a subsidy from the shade trees.Erythrina sp. andInga sp. are potential nitrogen fixers although we found no active sites during the dry period sampled. The average litter decomposition constant, k, expressed in terms of nitrogen, was estimated as 4.5, equivalent to a half-life of approximately two months.     

Regional gains and losses of nitrogen in the Amazon basin

In order to better understand the relative importance of different ecosystems and nitrogen cycling processes within the Amazon basin to the nitrogen economy of this region, we constructed a generalized nitrogen budget for the region based on data for hydrologic losses of nitrogen and nitrogen fixation in Amazon forests. Data included information available for nitrogen in water entering and leaving both the entire basin and watersheds on oxisol and ultisol soils near Manaus, Brazil, in addition to biological nitrogen fixation in forests on ultisol, oxisol and entisol (‘varzea’) soils in Central Amazonia. Available data indicate that 4–6 kg N ha^?1 yr^?1 are lost via the River Amazonas, and that a similar amount enters in rainfall. Root-associated biological nitrogen fixation contributesca. 2 kg N ha^?1 yr^?1 to forests on oxisols, 20 kg N ha^?1 yr^?1 to forests on utisols, and 200 kg N ha^?1 yr^?1 to forests on fertile varzea soils. There is 5–10 fold more NH₄ ⁺?N than NO₃?N in rain and stream water entering and leaving the waterbasin near Manaus. Calculations based on these data plus certain assumption yield the following regional nitrogen balance estimate: inputs through bulk deposition of 36×10⁸ kg N yr^?1 and through biological nitrogen fixation of 120×10⁸ kg N yr^?1, and outputsvia the River Amazonas of 36×10⁸ kg N yr^?1 andvia denitrification and volatization (by difference) of 120×10⁸ kg N yr^?1.     

Nitrogen cycling in a flooded-soil ecosystem planted to rice (Oryza sativa L.)

¹⁵N studies of various aspects of the nitrogen cycle in a flooded rice ecosystem on Crowley silt loam soil in Louisiana were reviewed to construct a mass balance model of the nitrogen cycle for this system. Nitrogen transformations modeled included 1) net ammonification (0.22 mg NH₄ ⁺?N kg dry soil^?1 day^?1), 2) net nitrification (2.07 mg NO₃ ^??N kg^?1 dry soil^?1 day^?1), 3) denitrification (0.37 mg N kg dry soil^?1 day^?1), and 4) biological N₂ fixation (0.16 mg N kg dry soil^?1 day^?1). Nitrogen inputs included 1) application of fertilizers, 2) incorporation of crop residues, 3) biological N₂ fixation, and 4) deposition. Nitrogen outputs included 1) crop removal, 2) gaseous losses from NH₃ volatilization and simultaneous occurrence of nitrification-denitrification, and 3) leaching and runoff. Mass balance calculations indicated that 33% of the available inorganic nitrogen was recovered by rice, and the remaining nitrogen was lost from the system. Losses of N due to ammonia volatilization were minimal because fertilizer-N was incorporated into the soil. A significant portion of inorganic-N was lost by ammonium diffusion from the anaerobic layer to the aerobic layer in response to a concentration gradient and subsequent nitrification in the aerobic layer followed by nitrate diffusion into the anaerobic layer and denitrification into gaseous end products. Leaching and surface runoff losses were minimal.     

High retention of 15N‐labeled nitrogen deposition in a nitrogen saturated old‐growth tropical forest

The effects of increased reactive nitrogen (N) deposition in forests depend largely on its fate in the ecosystems. However, our knowledge on the fates of deposited N in tropical forest ecosystems and its retention mechanisms is limited. Here, we report the results from the first whole ecosystem ¹⁵N labeling experiment performed in a N‐rich old‐growth tropical forest in southern China. We added ¹⁵N tracer monthly as ¹⁵NH₄¹⁵NO₃ for 1 year to control plots and to N‐fertilized plots (N‐plots, receiving additions of 50 kg N ha^?1 yr^?1 for 10 years). Tracer recoveries in major ecosystem compartments were quantified 4 months after the last addition. Tracer recoveries in soil solution were monitored monthly to quantify leaching losses. Total tracer recovery in plant and soil (N retention) in the control plots was 72% and similar to those observed in temperate forests. The retention decreased to 52% in the N‐plots. Soil was the dominant sink, retaining 37% and 28% of the labeled N input in the control and N‐plots, respectively. Leaching below 20 cm was 50 kg N ha^?1 yr^?1 in the control plots and was close to the N input (51 kg N ha^?1 yr^?1), indicating N saturation of the top soil. Nitrogen addition increased N leaching to 73 kg N ha^?1 yr^?1. However, of these only 7 and 23 kg N ha^?1 yr^?1 in the control and N‐plots, respectively, originated from the labeled N input. Our findings indicate that deposited N, like in temperate forests, is largely incorporated into plant and soil pools in the short term, although the forest is N‐saturated, but high cycling rates may later release the N for leaching and/or gaseous loss. Thus, N cycling rates rather than short‐term N retention represent the main difference between temperate forests and the studied tropical forest.     

Nitrogen dynamics and soil nitrate retention in a <Emphasis Type="Italic">Coffea arabica</Emphasis>—<Emphasis Type="Italic">Eucalyptus deglupta</Emphasis> agroforestry system in Southern Costa Rica

Nitrogen fertilization is a key factor for coffee production but creates a risk of water contamination through nitrate (NO₃⁻) leaching in heavily fertilized plantations under high rainfall. The inclusion of fast growing timber trees in these coffee plantations may increase total biomass and reduce nutrient leaching. Potential controls of N loss were measured in an unshaded coffee (Coffea arabica L.) plot and in an adjacent coffee plot shaded with the timber species Eucalyptus deglupta Blume (110 trees ha⁻¹), established on an Acrisol that received 180 kg N ha⁻¹ as ammonium-nitrate and 2,700 mm yr⁻¹ rainfall. Results of the one year study showed that these trees had little effect on the N budget although some N fluxes were modified. Soil N mineralization and nitrification rates in the 0–20 cm soil layer were similar in both systems (≈280 kg N ha⁻¹ yr⁻¹). N export in coffee harvest (2002) was 34 and 25 kg N ha⁻¹ yr⁻¹ in unshaded and shaded coffee, and N accumulation in permanent biomass and litter was 25 and 45 kg N ha⁻¹ yr⁻¹, respectively. The losses in surface runoff (≈0.8 kg mineral N ha⁻¹ yr⁻¹) and N₂O emissions (1.9 kg N ha⁻¹ yr⁻¹) were low in both cases. Lysimeters located at 60, 120, and 200 cm depths in shaded coffee, detected average concentrations of 12.9, 6.1 and 1.2 mg NO₃⁻-N l⁻¹, respectively. Drainage was slightly reduced in the coffee-timber plantation. NO₃⁻ leaching at 200 cm depth was about 27 ± 10 and 16 ± 7 kg N ha⁻¹ yr⁻¹ in unshaded and shaded coffee, respectively. In both plots, very low NO₃⁻ concentrations in soil solution at 200 cm depth (and in groundwater) were apparently due to NO₃⁻ adsorption in the subsoil but the duration of this process is not presently known. In these conventional coffee plantations, fertilization and agroforestry practices must be refined to match plant needs and limit potential NO₃⁻ contamination of subsoil and shallow soil water.     

Comparing annual and perennial crops for bioenergy production – influence on nitrate leaching and energy balance

Production of energy crops is promoted as a means to mitigate global warming by decreasing dependency on fossil energy. However, agricultural production of bioenergy can have various environmental effects depending on the crop and production system. In a field trial initiated in 2008, nitrate concentration in soil water was measured below winter wheat, grass‐clover and willow during three growing seasons. Crop water balances were modelled to estimate the amount of nitrate leached per hectare. In addition, dry matter yields and nitrogen (N) yields were measured, and N balances and energy balances were calculated. In willow, nitrate concentrations were up to approximately 20 mg l^?1 nitrate‐N during the establishment year, but declined subsequently to <5 mg l^?1 nitrate‐N, resulting in an annual N leaching loss of 18, 3 and 0.3 kg ha^?1 yr^?1 N in the first 3 years after planting. A similar trend was observed in grass‐clover where concentrations stabilized at 2–4 mg l^?1 nitrate‐N from the beginning of the second growing season, corresponding to leaching of approximately 5 kg ha^?1 yr^?1 N. In winter wheat, an annual N leaching loss of 36–68 kg ha^?1 yr^?1 was observed. For comparison, nitrate leaching was also measured in an old willow crop established in 1996 from which N leaching ranged from 6 to 27 kg ha^?1 yr^?1. Dry matter yields ranged between 5.9 and 14.8 Mg yr^?1 with lowest yield in the newly established willow and the highest yield harvested in grass‐clover. Grass‐clover gave the highest net energy yield of 244 GJ ha^?1 yr^?1, whereas old willow, winter wheat and first rotation willow gave net energy yields of 235, 180 and 105 GJ ha^?1 yr^?1. The study showed that perennial crops can provide high energy yields and significantly reduce N losses compared to annual crops.     

Nitrogen transformations in two nitrogen saturated forest ecosystems subjected to an experimental decrease in nitrogen deposition

Nitrogen transformations were studied in the forest floor and mineral soil (0–5 cm) of a Douglas fir forest (Pseudotsuga menziesii (Mirb.) Franco.) and a Scots pine forest (Pinus sylvestris L.) in the Netherlands. Curren nitrogen depositions (40 and 56 kg N ha^-1 yr^-1, respectively) were reduced to natural background levels (1–2 kg N ha^-1 yr^-1) by a roof construction. The study concentrated on rates and dynamic properties of nitrogen transformations and their link with the leaching pattern and nitrogen uptake of the vegetation under high and reduced nitrogen deposition levels. Results of an in situ field incubation experiment and laboratory incubations were compared. No effect of the reduced N deposition on nitrogen transformations was found in the Douglas fir forest. In the Scots pine forest, however, during some periods of the year nitrogen transformations were significantly decreased under the low nitrogen deposition level. At low nitrogen inputs a net immobilization occurred during most of the year leading to a very small net mineralization for the whole year. In laboratory and in individual field plots nitrogen transformations were negatively correlated with initial inorganic nitrogen concentrations. Nitrogen budget estimates showed that nitrogen transformations were probably underestimated by the in situ incubation technique. Nevertheless less nitrogen was available for plant uptake and leaching at the low deposition plots.     

A long‐term nitrogen fertilizer gradient has little effect on soil organic matter in a high‐intensity maize production system

Global maize production alters an enormous soil organic C (SOC) stock, ultimately affecting greenhouse gas concentrations and the capacity of agroecosystems to buffer climate variability. Inorganic N fertilizer is perhaps the most important factor affecting SOC within maize‐based systems due to its effects on crop residue production and SOC mineralization. Using a continuous maize cropping system with a 13 year N fertilizer gradient (0–269 kg N ha^?1 yr^?1) that created a large range in crop residue inputs (3.60–9.94 Mg dry matter ha^?1 yr^?1), we provide the first agronomic assessment of long‐term N fertilizer effects on SOC with direct reference to N rates that are empirically determined to be insufficient, optimum, and excessive. Across the N fertilizer gradient, SOC in physico‐chemically protected pools was not affected by N fertilizer rate or residue inputs. However, unprotected particulate organic matter (POM) fractions increased with residue inputs. Although N fertilizer was negatively linearly correlated with POM C/N ratios, the slope of this relationship decreased from the least decomposed POM pools (coarse POM) to the most decomposed POM pools (fine intra‐aggregate POM). Moreover, C/N ratios of protected pools did not vary across N rates, suggesting little effect of N fertilizer on soil organic matter (SOM) after decomposition of POM. Comparing a N rate within 4% of agronomic optimum (208 kg N ha^?1 yr^?1) and an excessive N rate (269 kg N ha^?1 yr^?1), there were no differences between SOC amount, SOM C/N ratios, or microbial biomass and composition. These data suggest that excessive N fertilizer had little effect on SOM and they complement agronomic assessments of environmental N losses, that demonstrate N₂O and NO₃ emissions exponentially increase when agronomic optimum N is surpassed.     

Nitrous oxide emissions and nitrate leaching from a rain-fed wheat-maize rotation in the Sichuan Basin, China

Aims

A 3-year field experiment (October 2004–October 2007) was conducted to quantify N₂O fluxes and determine the regulating factors from rain-fed, N fertilized wheat-maize rotation in the Sichuan Basin, China.

Methods

Static chamber-GC techniques were used to measure soil N₂O fluxes in three treatments (three replicates per treatment): CK (no fertilizer); N150 (300 kg N fertilizer ha^?1 yr^?1 or 150 kg N?ha^?1 per crop); N250 (500 kg N fertilizer ha^?1 yr^?1 kg or 250 kg N?ha^?1 per crop). Nitrate (NO ₃ ^? ) leaching losses were measured at nearby sites using free-drained lysimeters.

Results

The annual N₂O fluxes from the N fertilized treatments were in the range of 1.9 to 6.7 kg N?ha^?1 yr^?1 corresponding to an N₂O emission factor ranging from 0.12 % to 1.06 % (mean value: 0.61 %). The relationship between monthly soil N₂O fluxes and NO ₃ ^- leaching losses can be described by a significant exponential decaying function.

Conclusions

The N₂O emission factor obtained in our study was somewhat lower than the current IPCC default emission factor (1 %). Nitrate leaching, through removal of topsoil NO ₃ ^? , is an underrated regulating factor of soil N₂O fluxes from cropland, especially in the regions where high NO ₃ ^- leaching losses occur.     

Biochar application as a tool to decrease soil nitrogen losses (NH3 volatilization,N2O emissions,and N leaching) from croplands: Options and mitigation strength in a global perspective

Biochar application to croplands has been proposed as a potential strategy to decrease losses of soil‐reactive nitrogen (N) to the air and water. However, the extent and spatial variability of biochar function at the global level are still unclear. Using Random Forest regression modelling of machine learning based on data compiled from the literature, we mapped the impacts of different biochar types (derived from wood, straw, or manure), and their interactions with biochar application rates, soil properties, and environmental factors, on soil N losses (NH₃ volatilization, N₂O emissions, and N leaching) and crop productivity. The results show that a suitable distribution of biochar across global croplands (i.e., one application of <40 t ha^?1 wood biochar for poorly buffered soils, such as those characterized by soil pH<5, organic carbon<1%, or clay>30%; and one application of <80 t ha^?1 wood biochar, <40 t ha^?1 straw biochar, or <10 t ha^?1 manure biochar for other soils) could achieve an increase in global crop yields by 222–766 Tg yr^?1 (4%–16% increase), a mitigation of cropland N₂O emissions by 0.19–0.88 Tg N yr^?1 (6%–30% decrease), a decline of cropland N leaching by 3.9–9.2 Tg N yr^?1 (12%–29% decrease), but also a fluctuation of cropland NH₃ volatilization by ?1.9–4.7 Tg N yr^?1 (?12%–31% change). The decreased sum of the three major reactive N losses amount to 1.7–9.4 Tg N yr^?1, which corresponds to 3%–14% of the global cropland total N loss. Biochar generally has a larger potential for decreasing soil N losses but with less benefits to crop production in temperate regions than in tropical regions.     

Dry deposition of ammonia gas drives species change faster than wet deposition of ammonium ions: evidence from a long‐term field manipulation

Although the effects of atmospheric nitrogen deposition on species composition are relatively well known, the roles of the different forms of nitrogen, in particular gaseous ammonia (NH₃), have not been tested in the field. Since 2002, we have manipulated the form of N deposition to an ombrotrophic bog, Whim, on deep peat in southern Scotland, with low ambient N (wet + dry = 8 kg N ha^?1 yr^?1) and S (4 kg S ha^?1 yr^?1) deposition. A gradient of ammonia (NH₃, dry N), from 70 kg N ha^?1 yr^?1 down to background, 3–4 kg N ha^?1 yr^?1 was generated by free air release. Wet ammonium (NH₄⁺, wet N) was provided to replicate plots in a fine rainwater spray (NH₄Cl at +8, +24, +56 kg N ha^?1 yr^?1). Automated treatments are coupled to meteorological conditions, in a globally unique, field experiment. Ammonia concentrations were converted to NH₃‐N deposition (kg N ha^?1) using a site/vegetation specific parameterization. Within 3 years, exposure to relatively modest deposition of NH₃, 20–56 kg NH₃‐N ha^?1 yr^?1 led to dramatic reductions in species cover, with almost total loss of Calluna vulgaris, Sphagnum capillifolium and Cladonia portentosa. These effects appear to result from direct foliar uptake and interaction with abiotic and biotic stresses, rather than via effects on the soil. Additional wet N by contrast, significantly increased Calluna cover after 5 years at the 56 kg N dose, but reduced cover of Sphagnum and Cladonia. Cover reductions caused by wet N were significantly different from and much smaller than those caused by equivalent dry N doses. The effects of gaseous NH₃ described here, highlight the potential for ammonia to destroy acid heathland and peat bog ecosystems. Separating the effects of gaseous ammonia and wet ammonium deposition, for a peat bog, has significant implications for regulatory bodies and conservation agencies.     

Does N fertiliser regime influence N leaching and quality of different-aged turfgrass (Pennisetum clandestinum) stands?

The effects of N fertiliser regimes on N leaching and turfgrass quality during the establishment and maintenance of Kikuyu turfgrass (Pennisetum clandestinum (Holst. Ex Chiov)) were evaluated in a 24 month field study. Treatments included two turfgrass ages (established from 20 week or 20 year old turfgrass, the later included a 50 mm ‘mat’ layer), three N application rates (50, 100 or 150 kg N ha^?1 yr^?1) and three application frequencies (every 4 weeks, 4 applications per year, 2 applications per year); and included turfgrass plots that received no N fertiliser. Nitrogen leaching, measured using soil lysimeters, ranged from 35 to 69 kg N ha^?1 by the end of 24 months, and varied with turfgrass age, but not N fertiliser regime. Greatest N losses occurred during turfgrass establishment, with up to 50% of all N leached in the organic form. We recommend measuring both total N and mineral N when assessing N leaching from turfgrass. The quality of the older turfgrass was maintained using less N fertiliser than the younger turfgrass, while increasing N application frequency improved the consistency of turfgrass growth and colour.     

Nitrogen input together with ecosystem nitrogen enrichment predict nitrate leaching from European forests

The IFEF database (Indicators of Forest Ecosystem Functioning), consisting of nitrogen deposition, nitrate leaching fluxes, and soil and ecosystem characteristics, is analysed to evaluate the C/N ratio in the organic horizon as an indicator of nitrate leaching. One hundred and eighty one forests are examined, from countries across Europe ranging from boreal to Mediterranean regions, encompassing broadleaf and coniferous sites and plot and catchment studies. N input in throughfall ranges from less than 1 kg N ha^?1 y^?1 in northern Norway and Finland to greater than 60 kg N ha^?1 y^?1 in the Netherlands and Czech Republic. The amount of NO₃^– leached covers a smaller range, between 1 and 40 kg N ha^?1 y^?1. Nitrate leaching is strongly dependent on the amount of nitrogen deposited in throughfall (N input) and simply adding the C/N ratio in the organic horizon to a regression equation does not improve this relationship. However, when the data are stratified based on C/N ratios less than or equal to 25 and greater than 25, highly significant relationships (P < 0.05) are observed between N input and NO₃^– leached. The slope of the relationship for those sites where C/N ratio is ≤ 25 (′nitrogen enriched′ sites) is twice that for those sites where C/N ratio is > 25. These empirical relationships may be used to identify which forested ecosystems are likely to show elevated rates of nitrate leaching under predicted future nitrogen deposition scenarios. Elevated NO₃^– leaching also shows a relationship with soil pH, with high rates of NO₃^– leaching only observed at sites with a pH < 4.5 and N inputs > 30 kg N ha^?1 y^?1. Tree age and species have no significant impact on the ecosystem response to N input at a regional scale.     

Postfire nitrogen balance of Mediterranean shrublands: Direct combustion losses versus gaseous and leaching losses from the postfire soil mineral nitrogen flush

Fire is a major factor controlling global carbon (C) and nitrogen (N) cycling. While direct C and N losses caused by combustion have been comparably well established, important knowledge gaps remain on postfire N losses. Here, we quantified both direct C and N combustion losses as well as postfire gaseous losses (N₂O, NO and N₂) and N leaching after a high‐intensity experimental fire in an old shrubland in central Spain. Combustion losses of C and N were 9.4 Mg C/ha and 129 kg N/ha, respectively, representing 66% and 58% of initial aboveground vegetation and litter stocks. Moreover, fire strongly increased soil mineral N concentrations by several magnitudes to a maximum of 44 kg N/ha 2 months after the fire, with N largely originating from dead soil microbes. Postfire soil emissions increased from 5.4 to 10.1 kg N ha^?1 year^?1 for N₂, from 1.1 to 1.9 kg N ha^?1 year^?1 for NO and from 0.05 to 0.2 kg N ha^?1 year^?1 for N₂O. Maximal leaching losses occurred 2 months after peak soil mineral N concentrations, but remained with 0.1 kg N ha^?1 year^?1 of minor importance for the postfire N mass balance. ¹⁵N stable isotope labelling revealed that 33% of the mineral N produced by fire was incorporated in stable soil N pools, while the remainder was lost. Overall, our work reveals significant postfire N losses dominated by emissions of N₂ that need to be considered when assessing fire effects on ecosystem N cycling and mass balance. We propose indirect N gas emissions factors for the first postfire year, equalling to 7.7% (N₂‐N), 2.7% (NO‐N) and 5.0% (N₂O‐N) of the direct fire combustion losses of the respective N gas species.     

Cycling of nitrogen in modern agricultural systems

Summary Agro-ecosystems have developed from mixed- and multiple-cropping systems with relatively closed N cycles to intensively managed monocultures with large N inputs in the form of commercial fertilizers. Cultivation of increasingly larger areas of land has resulted in substantial losses of soil organic matter and N. Also, the move from slash and burn agriculture to intensively ploughed systems has resulted in losses through increased erosion.The use of N fertilizers has increased rapidly toca. 60 Tg N yr^–1 (1980/81), which is equivalent to at least 40% of the N fixed biologically in all terrestrial systems and 36% more than is fixed in all croplands. On a global scale, the major losses of N from agro-ecosystems are estimated to be: harvest, 30 Tg; leaching, 2 Tg; erosion, 2–20 Tg; denitrification 1–44 Tg; and ammonia volatilization, 13–23 Tg. However, the data base is very crude and several estimates may be wrong by as much as one order of magnitude.Additions of N fertilizers have both direct and indirect effects on soil microorganisms. The possible importance of such effects is briefly discussed and a specific example is given on long-term effects on soil microbial biomass and nitrification rates in 27-year-old cropping systems with different N additions: (i) 0 kg N ha^–1 yr^–1, (ii) 80 kg N ha^–1 yr^–1, (iii) farmyard manureca. 80 kg N ha^–1 yr^–1.Few detailed N budgets exist for agro-ecosystems, despite its major importance as a limiting plant nutrient and the large losses of N from such systems. In conclusion, preliminary nitrogen budgets for four cropping systems (barley receiving 0 or 120 kg N ha^–1 yr^–1; meadow fescue ley with 200 kg N ha^–1 yr^–1 and a lucerne ley) are presented, with special attention to N flow through the soil organisms.Keynote address     

Nitrogen biogeochemistry of a mature Scots pine forest subjected to high nitrogen loads

Nitrogen (N) biogeochemistry of a mature Scots pine (Pinus sylvestris L.) stand subjected to an average total atmospheric N deposition of 48 kg ha^?1 year^?1 was studied during the period 1992–2007. The annual amount of dissolved inorganic nitrogen (DIN) in throughfall (TF) averaged 34 kg ha^?1 year^?1 over the 16-year monitoring period. The throughfall fluxes contained also considerable amounts of dissolved organic nitrogen (DON) (5–8.5 kg N ha^?1 year^?1), which should be incorporated in the estimate of N flux using throughfall collectors. Throughfall DIN fluxes declined at a rate of ?0.9 kg N ha^?1 year^?1, mainly due to the decreasing TF fluxes of ammonium (NH₄), which accounted for 70% to TF DIN. The decrease in TF DIN was accompanied by a decrease in DIN leaching in the seepage water (?1.6 kg N ha^?1 year^?1), which occurred exclusively as nitrate (NO₃ ^?). Nitrate losses in the leachate of the forest floor (LFH) equalled the TF NO₃ ^? delivered to the LFH-layer. On the contrary, about half of the TF NH₄ ⁺ was retained within the LFH-layer. Approximately 60% of the TF DIN fluxes were leached indicating that N inputs were far in excess of the N requirements of the forest. For DON, losses were only substantial from the LFH-layer, but no DON was leached in the seepage water. Despite the high N losses through nitrate leaching and NO _x emission, the forest was still accumulating N, especially in the aggrading LFH-layer. The forest stand, on the contrary, was found to be a poor N sink.     

Germination, field establishment patterns and nitrogen fixation of indigenous legumes on nutrient-depleted soils

Integrating N₂-fixing indigenous legumes in smallholder farming systems has potential to alleviate some of the major soil fertility constraints associated with lack of nitrogen (N) inputs in many parts of Sub-SaharanAfrica. Studies were conducted under low (450–650 mm yr^?1) and high (>800 mm yr^?1) rainfall areas in Zimbabwe to investigate the establishment and nitrogen fixation patterns of fifteen indigenous legume species. The legume seeds were broadcast in mixtures at 120 seeds m^?2 species^?1 during 2004/05 and 2005/06 rainfall seasons.Eriosema ellipticum, Crotalaria ochroleuca andC. pallida had emergence rates above 15% compared with <10% forTephrosia radicans andIndigofera astragalina. Seed hardness accounted for >50% germination failure, while low viability explained 10–30%.Crotalaria ochroleuca andC. pallida attained a maximum biomass of 5–9 t ha^?1 (dry weight) over six months, while species that reached peak biomass over three months (e.g.C. cylindrostachys andC. glauca) gave lowest yields of ≈0.5 t ha^?1. Biennials,Neonotonia wightii, E. ellipticum and Tephrosia radicans, exhibited slow growth rates and only attained their maximum biomass of ≈2 t ha^?1 in the second season. The legumes derived 60–99% of their N from the atmosphere, fixing 5–120 kg N ha^?1 under low rainfall and 78–267 kg N ha^?1 under high rainfall. These findings suggest that the legumes could contribute in restoring productivity of soils continuously cultivated with little or no nutrient inputs in most of Zimbabwe and similar agro-ecologies in SubSaharan Africa.