Enhanced‐efficiency fertilizers are not a panacea for resolving the nitrogen problem

Improving nitrogen (N) management for greater agricultural output while minimizing unintended environmental consequences is critical in the endeavor of feeding the growing population sustainably amid climate change. Enhanced‐efficiency fertilizers (EEFs) have been developed to better synchronize fertilizer N release with crop uptake, offering the potential for enhanced N use efficiency (NUE) and reduced losses. Can EEFs play a significant role in helping address the N management challenge? Here we present a comprehensive analysis of worldwide studies published in 1980–2016 evaluating four major types of EEFs (polymer‐coated fertilizers PCF, nitrification inhibitors NI, urease inhibitors UI, and double inhibitors DI, i.e. urease and nitrification inhibitors combined) regarding their effectiveness in increasing yield and NUE and reducing N losses. Overall productivity and environmental efficacy depended on the combination of EEF type and cropping systems, further affected by biophysical conditions. Best scenarios include: (i) DI used in grassland (n = 133), averaging 11% yield increase, 33% NUE improvement, and 47% decrease in aggregated N loss (sum of NO₃^‐, NH₃, and N₂O, totaling 84 kg N/ha); (ii) UI in rice‐paddy systems (n = 100), with 9% yield increase, 29% NUE improvement, and 41% N‐loss reduction (16 kg N/ha). EEF efficacies in wheat and maize systems were more complicated and generally less effective. In‐depth analysis indicated that the potential benefits of EEFs might be best achieved when a need is created, for example, by downward adjusting N application from conventional rate. We conclude that EEFs can play a significant role in sustainable agricultural production but their prudent use requires firstly eliminating any fertilizer mismanagement plus the implementation of knowledge‐based N management practices.     

Using nitrification inhibitors to mitigate agricultural N2O emission: a double‐edged sword?

Nitrification inhibitors show promise in decreasing nitrous oxide (N₂O) emission from agricultural systems worldwide, but they may be much less effective than previously thought when both direct and indirect emissions are taken into account. Whilst nitrification inhibitors are effective at decreasing direct N₂O emission and nitrate (NO₃^–) leaching, limited studies suggest that they may increase ammonia (NH₃) volatilization and, subsequently, indirect N₂O emission. These dual effects are typically not considered when evaluating the inhibitors as a climate change mitigation tool. Here, we collate results from the literature that simultaneously examined the effects of nitrification inhibitors on N₂O and NH₃ emissions. We found that nitrification inhibitors decreased direct N₂O emission by 0.2–4.5 kg N₂O‐N ha^?1 (8–57%), but generally increased NH₃ emission by 0.2–18.7 kg NH₃‐N ha^?1 (3–65%). Taking into account the estimated indirect N₂O emission from deposited NH₃, the overall impact of nitrification inhibitors ranged from ?4.5 (reduction) to +0.5 (increase) kg N₂O‐N ha^?1. Our results suggest that the beneficial effect of nitrification inhibitors in decreasing direct N₂O emission can be undermined or even outweighed by an increase in NH₃ volatilization.     

Can knowledge‐based N management produce more staple grain with lower greenhouse gas emission and reactive nitrogen pollution? A meta‐analysis

Knowledge‐based nitrogen (N) management, which is designed for a better synchronization of crop N demand with N supply, is critical for global food security and environmental sustainability. Yet, a comprehensive assessment on how these N management practices affect food production, greenhouse gas emission (GHG), and N pollution in China is lacking. We compiled the results of 376 studies (1166 observations) to evaluate the overall effects of seven knowledge‐based N management practices on crop productivity, nitrous oxide (N₂O) emission, and major reactive N (Nr) losses (ammonia, NH₃; N leaching and runoff), for staple grain (rice, wheat, and corn) production in China. These practices included the application of controlled‐release N fertilizer, nitrification inhibitor (NI) and urease inhibitor (UI), higher splitting frequency of fertilizer N application, lower basal N fertilizer (BF) proportion, deep placement of N fertilizer, and optimal N rate based on soil N test. Our results showed that, compared to traditional N management, these knowledge‐based N practices significantly increased grain yields by 1.3–10.0%, which is attributed to the higher aboveground N uptake (5.1–12.1%) and N use efficiency in grain (8.0–48.2%). Moreover, these N management practices overall reduced GHG emission and Nr losses, by 5.4–39.8% for N₂O emission, 30.7–61.5% for NH₃ emission (except for the NI application), 13.6–37.3% for N leaching, and 15.5–45.0% for N runoff. The use of NI increased NH₃ emission by 27.5% (9.0–56.0%), which deserves extra‐attention. The cost and benefit analysis indicated that the yield profit of these N management practices exceeded the corresponding input cost, which resulted in a significant increase of the net economic benefit by 2.9–12.6%. These results suggest that knowledge‐based N management practice can be considered an effective way to ensure food security and improve environmental sustainability, while increasing economic return.     

Nitrogen addition alters mineralization dynamics of 13C‐depleted leaf and twig litter and reduces leaching of older DOC from mineral soil

Recent reviews indicate that N deposition increases soil organic matter (SOM) storage in forests but the undelying processes are poorly understood. Our aim was to quantify the impacts of increased N inputs on soil C fluxes such as C mineralization and leaching of dissolved organic carbon (DOC) from different litter materials and native SOM. We added 5.5 g N m^?2 yr^?1 as NH₄NO₃ over 1 year to two beech forest stands on calcareous soils in the Swiss Jura. We replaced the native litter layer with ¹³C‐depleted twigs and leaves (δ¹³C: ?38.4 and ?40.8‰) in late fall and measured N effects on litter‐ and SOM‐derived C fluxes. Nitrogen addition did not significantly affect annual C losses through mineralization, but altered the temporal dynamics in litter mineralization: increased N inputs stimulated initial mineralization during winter (leaves: +25%; twigs: +22%), but suppressed rates in the subsequent summer. The switch from a positive to a negative response occurred earlier and more strongly for leaves than for twigs (?21% vs. 0%). Nitrogen addition did not influence microbial respiration from the nonlabeled calcareous mineral soil below the litter which contrasts with recent meta‐analysis primarily based on acidic soils. Leaching of DOC from the litter layer was not affected by NH₄NO₃ additions, but DOC fluxes from the mineral soils at 5 and 10 cm depth were significantly reduced by 17%. The ¹³C tracking indicated that litter‐derived C contributed less than 15% of the DOC flux from the mineral soil, with N additions not affecting this fraction. Hence, the suppressed DOC fluxes from the mineral soil at higher N inputs can be attributed to reduced mobilization of nonlitter derived ‘older’ DOC. We relate this decline to an altered solute chemistry by NH₄NO₃ additions, an increased ionic strength and acidification resulting from nitrification, rather than to a change in microbial decomposition.     

Nitrogen deposition and forest nitrogen cycling along an urban–rural transect in southern China

There is increasing concern over the impact of atmospheric nitrogen (N) deposition on forest ecosystems in the tropical and subtropical areas. In this study, we quantified atmospheric N deposition and revealed current plant and soil N status in 14 forests along a 150 km urban to rural transect in southern China, with an emphasis on examining whether foliar δ¹⁵N can be used as an indicator of N saturation. Bulk deposition ranged from 16.2 to 38.2 kg N ha^?1 yr^?1, while the throughfall covered a larger range of 11.7–65.1 kg N ha^?1 yr^?1. Foliar N concentration, NO₃^? leaching to stream, and soil NO₃^? concentration were low and NO₃^? production was negligible in some rural forests, indicating that primary production in these forests may be limited by N supply. But all these N variables were enhanced in suburban and urban forests. Across the study transect, throughfall N input was correlated positively with soil nitrification and NO₃^? leaching to stream, and negatively with pH values in soil and stream water. Foliar δ¹⁵N was between ?6.6‰ and 0.7‰, and was negatively correlated with soil NO₃^? concentration and NO₃^? leaching to stream across the entire transect, demonstrating that an increased N supply does not necessarily increase forest δ¹⁵N values. We proposed several potential mechanism that could contribute to the δ¹⁵N pattern, including (1) increased plant uptake of ¹⁵N‐depleted soil NO₃^?, (2) foliage uptake of ¹⁵N‐depleted NH₄⁺, (3) increased utilization of soil inorganic N relative to dissolved organic N, and (4) increased fractionation during plant N uptake under higher soil N availability.     

The contribution of nitrogen transformation processes to total N2O emissions from soils used for intensive vegetable cultivation

The rapid expansion of intensively farmed vegetable fields has substantially contributed to the total N₂O emissions from croplands in China. However, to date, the mechanisms underlying this phenomenon have not been completely understood. To quantify the contributions of autotrophic nitrification, heterotrophic nitrification, and denitrification to N₂O production from the intensive vegetable fields and to identify the affecting factors, a ¹⁵N tracing experiment was conducted using five soil samples collected from adjacent fields used for rice-wheat rotation system (WF), or for consecutive vegetable cultivation (VF) for 0.5 (VF1), 6 (VF2), 8 (VF3), and 10 (VF4) years. Soil was incubated under 50% water holding capacity (WHC) at 25°C for 96 h after being labeled with ¹⁵NH₄NO₃ or NH ₄ ¹⁵ NO₃. The average N₂O emission rate was 24.2 ng N?kg^?1 h^?1 in WF soil, but it ranged from 69.6 to 507 ng N?kg^?1 h^?1 in VF soils. Autotrophic nitrification, heterotrophic nitrification and denitrification accounted for 0.3–31.4%, 25.4–54.4% and 22.5–57.7% of the N₂O emissions, respectively. When vegetable soils were moderately acidified (pH, 6.2 to ?≥?5.7), the increased N₂O emissions resulted from the increase of both the gross autotrophic and heterotrophic nitrification rates and the N₂O product ratio of autotrophic nitrification. However, once severe acidification occurred (as in VF4, pH?≤?4.3) and salt stress increased, both autotrophic and heterotrophic nitrification rates were inhibited to levels similar to those of WF soil. The enhanced N₂O product ratios of heterotrophic nitrification (4.84‰), autotrophic nitrification (0.93‰) and denitrification processes were the most important factors explaining high N₂O emission in VF4 soil. Data from this study showed that various soil conditions (e.g., soil salinity and concentration of NO ₃ ^- or NH ₄ ⁺ ) could also significantly affect the sources and rates of N₂O emission.     

氮肥配施生化抑制剂组合对黄泥田土壤氮素淋溶特征的影响

揭示尿素类肥料添加生化抑制剂组合后,在黄泥田土壤中硝态氮(NO~-_3-N)和铵态氮(NH~+_4-N)的淋溶损失规律。采用室内土柱淋溶培养试验,研究脲酶抑制剂N-丁基硫代磷酰三胺(NBPT)和硝化抑制剂2-氯-6-(三氯甲基)吡啶(CP)单独添加及配合施用对尿素和尿素硝铵(300 kg N/hm~2)中氮(N)素在土体中淋溶损失的影响。结果表明:尿素和尿素硝铵处理淋溶液中NH~+_4-N和NO~-_3-N浓度均呈先升后降的变化趋势,而出峰时间不一。NH~+_4-N和NO~-_3-N淋失量随着时间的延长,处理间差异逐渐变大。NBPT处理可以减缓尿素水解,有效抑制NH~+_4-N生成,延缓其出峰时间,减少NH~+_4-N流失;CP处理可以有效抑制NH~+_4-N向NO~-_3-N转化,减少NO~-_3-N流失。与单独添加NBPT和CP处理相比,两者配施对N素淋溶损失有明显的协同抑制效果在黄泥田土壤中,既能减缓尿素水解,保持土壤中较高NH~+_4-N含量,又能降低淋溶液中NO~-_3-N浓度。培养结束时(第72天),UAN处理中NO~-_3-N、NH~+_4-N、矿质态N淋失总量及硝化率较U处理高34.39%、5.32%、31.72%和15.71%。U+NBPT、U+CP和U+NBPT+CP处理较U处理分别显著降低NO~-_3-N淋失总量达15.58%、114.77%和73.45%;UAN+NBPT、UAN+CP和UAN+NBPT+CP处理较UAN处理分别显著降低达15.88%、54.87%和37.46%。不同处理NO~-_3-N淋失总量大小表现为:UAN UAN+NBPT U UAN+NBPT+CP U+NBPT UAN+CP U+NBPT+CP U+CP CK。在一定施肥量条件下,NBPT和CP单独施用或配施均可降低黄泥田土壤中NO~-_3-N累积淋失量。对各处理淋溶液中NO~-_3-N淋失量(y)随时间(x)的变化进行拟合,其中以线性方程(y=ax+b)的拟合度较高,且各抑制剂处理a、b值均存在明显差异。总体认为,在黄泥田土壤中施用CP及其与NBPT配施可以显著降低土壤NO~-_3-N淋溶损失,减少N素淋失风险,提高肥料利用率。     

Contributions to nitrogen leaching and pasture uptake by autumn-applied dairy effluent and ammonium fertilizer labeled with 15N isotope

The objective of this study was to compare the N leaching loss and pasture N uptake from autumn-applied dairy shed effluent and ammonium fertilizer (NH₄Cl) labeled with ¹⁵N, using intact soil lysimeters (80 cm diameter, 120 cm depth). The soil used was a sandy loam, and the pasture was a mixture of perennial ryegrass (Lolium perenne) and white clover (Trifolium repens). The DSE and NH₄Cl were applied twice annually in autumn (May) and late spring (November), each at 200 kg N ha^-1. The N applied in May 1996 was labeled with ¹⁵N. The lysimeters were either spray or flood irrigated during the summer. The autumn-applied DSE resulted in lower N leaching losses compared with NH₄Cl. However, the N applied in the autumn had a higher potential for leaching than N applied in late spring. Between 4.5–8.1% of the ¹⁵N-labeled mineral N in the DSE and 15.1–18.8% of the ¹⁵N-labeled NH₄Cl applied in the autumn were leached within a year of application. Of the annual N leaching losses in the DSE treatments (16.0–26.9 kg N ha^-1), a fifth (20.3–22.9%) was from the mineral N fraction of the DSE applied in the autumn, with the remaining larger proportion from the organic fraction of the DSE, soil N and N applied in spring. In the NH₄Cl treatments, more than half (53.8–64.8%) of the annual N leaching loss (55.9–57.6 kg N ha^-1) was derived from the autumn-applied NH₄Cl. DSE was as effective as NH₄Cl in stimulating pasture production. Since only 4.4–4.5% of the annual herbage N uptake in the DSE treatment and 12.3–13.3% in the NH₄Cl treatment were derived from the autumn-applied mineral N, large proportions of the annual herbage N uptake must have been derived from the N applied in spring, the organic N fraction in the DSE, soil N and N fixed by clover. The recoveries of ¹⁵N in the herbage were similar between the DSE and the NH₄Cl treatments, but those in the leachate were over 50% less from the DSE than from the NH₄Cl treatment. The lower leaching loss of ¹⁵N in the DSE treatment was attributed to the stimulated microbial activities and increased immobilization following the application of DSE. This revised version was published online in June 2006 with corrections to the Cover Date.     

Isotopic evidence for the occurrence of biological nitrification and nitrogen deposition processing in forest canopies

This study examines the role of tree canopies in processing atmospheric nitrogen (N_dep) for four forests in the United Kingdom subjected to different N_dep: Scots pine and beech stands under high N_dep (HN, 13–19 kg N ha^?1 yr^?1), compared to Scots pine and beech stands under low N_dep (LN, 9 kg N ha^?1 yr^?1). Changes of NO₃‐N and NH₄‐N concentrations in rainfall (RF) and throughfall (TF) together with a quadruple isotope approach, which combines δ¹⁸O, Δ¹⁷O and δ¹⁵N in NO₃^? and δ¹⁵N in NH₄⁺, were used to assess N transformations by the canopies. Generally, HN sites showed higher NH₄‐N and NO₃‐N concentrations in RF compared to the LN sites. Similar values of δ¹⁵N‐NO₃^? and δ¹⁸O in RF suggested similar source of atmospheric NO₃^? (i.e. local traffic), while more positive values for δ¹⁵N‐NH₄⁺ at HN compared to LN likely reflected the contribution of dry NH_x deposition from intensive local farming. The isotopic signatures of the N‐forms changed after interacting with tree canopies. Indeed, ¹⁵N‐enriched NH₄⁺ in TF compared to RF at all sites suggested that canopies played an important role in buffering dry N_dep also at the low N_dep site. Using two independent methods, based on δ¹⁸O and Δ¹⁷O, we quantified for the first time the proportion of NO₃^? in TF, which derived from nitrification occurring in tree canopies at the HN site. Specifically, for Scots pine, all the considered isotope approaches detected biological nitrification. By contrast for the beech, only using the mixing model with Δ¹⁷O, we were able to depict the occurrence of nitrification within canopies. Our study suggests that tree canopies play an active role in the N cycling within forest ecosystems. Processing of N_dep within canopies should not be neglected and needs further exploration, with the combination of multiple isotope tracers, with particular reference to Δ¹⁷O.     

Soil and fertilizer nitrogen transformations under alternate flooding and drying moisture regimes

Summary A study of changes in NH₄ ⁺ and NO₃ ^––N in Maahas clay amended with (NH₄)₂SO₄ and subjected to 4 water regimes in the presence and absence of the nitrification inhibitor N-Serve (Nitrapyrin) showed that the mineral N was well conserved in the continoous regimes of 50% and 200% (soil weight basis) but suffered heavy losses due to nitrification-denitrification under alternate drying and flooding. N-Serve was effective in minimizing these losses.Another incubation study with 3 soils showed that after 10 cycles of flooding and drying (either at 60°C or 25°C), the ammonification of soil N was enhanced. Nitrification of soil as well as fertilizer NH₄ ⁺ was completely inhibited upto 4 weeks by the treatments involving drying at high temperature. Flooding and air drying at 25°C, on the other hand, enhanced ammonification of soil N but retarded nitrification. These treatments, however, enhanced both ammonification and nitrification of the applied NH₄ ⁺ fertilizer N. Under flooded conditions rate of NH₄ ⁺ production was faster in soils that were dried at 60°C or 25°C and then flooded as compared to air dried soils.It is concluded that N losses by nitrification-denitrification and related N transformations may be considerably altered by alternating moisture regimes. Flooding and drying treatments seem to retard nitrification of soil N but conserve that of fertilizer NH₄ ⁺ applied after these treatments.     

Net greenhouse gas balance in response to nitrogen enrichment: perspectives from a coupled biogeochemical model

Increasing reactive nitrogen (N) input has been recognized as one of the important factors influencing climate system through affecting the uptake and emission of greenhouse gases (GHG). However, the magnitude and spatiotemporal variations of N‐induced GHG fluxes at regional and global scales remain far from certain. Here we selected China as an example, and used a coupled biogeochemical model in conjunction with spatially explicit data sets (including climate, atmospheric CO₂, O₃, N deposition, land use, and land cover changes, and N fertilizer application) to simulate the concurrent impacts of increasing atmospheric and fertilized N inputs on balance of three major GHGs (CO₂, CH₄, and N₂O). Our simulations showed that these two N enrichment sources in China decreased global warming potential (GWP) through stimulating CO₂ sink and suppressing CH₄ emission. However, direct N₂O emission was estimated to offset 39% of N‐induced carbon (C) benefit, with a net GWP of three GHGs averaging ?376.3 ± 146.4 Tg CO₂ eq yr^?1 (the standard deviation is interannual variability of GWP) during 2000–2008. The chemical N fertilizer uses were estimated to increase GWP by 45.6 ± 34.3 Tg CO₂ eq yr^?1 in the same period, and C sink was offset by 136%. The largest C sink offset ratio due to increasing N input was found in Southeast and Central mainland of China, where rapid industrial development and intensively managed crop system are located. Although exposed to the rapidly increasing N deposition, most of the natural vegetation covers were still showing decreasing GWP. However, due to extensive overuse of N fertilizer, China's cropland was found to show the least negative GWP, or even positive GWP in recent decade. From both scientific and policy perspectives, it is essential to incorporate multiple GHGs into a coupled biogeochemical framework for fully assessing N impacts on climate changes.     

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.     

生物炭配施硝化/脲酶抑制剂对亚热带水稻土活性氮气体排放的影响

探究施用生物炭和脲酶抑制剂/硝化抑制剂对亚热带水稻土氮素硝化过程的调控作用、氨挥发和N₂O排放的温室效应潜能的影响,确定生物炭与硝化和脲酶抑制剂的最佳组合,可为削减施用氮肥带来的活性氮气体排放对环境的负面风险提供理论依据。本研究采用室内好气培养试验方式,以单施尿素(N)为对照,设置7个试验处理[尿素+生物炭(NB),尿素+硝化抑制剂(N+NI),尿素+脲酶抑制剂(N+UI),尿素+硝化抑制剂+脲酶抑制剂(N+NIUI),尿素+硝化抑制剂+生物炭(NB+NI),尿素+脲酶抑制剂+生物炭(NB+UI),尿素+硝化抑制剂+脲酶抑制剂+生物炭(NB+NIUI)],观测生物炭与脲酶抑制剂(NBPT)/硝化抑制剂(DMPP)配施下土壤无机氮含量、N₂O排放及氨挥发的变化动态。结果表明: 1)培养期间,与N处理(5.11 mg N·kg^-1·d^-1)相比,NB处理的土壤硝化速率常数显著增加33.9%,N+NI处理显著降低22.9%;NB处理显著提高了氨氧化细菌(AOB)丰度,增幅达56.0%。2)与N处理相比,N+NI和NB+NI处理的NH₃累积排放量均显著增加约49%;N+UI处理降低了NH₃累积损失量,NB+UI处理抑制效果更明显。3)各处理的N₂O排放速率高峰均出现在施肥后前10 d;NB处理的N₂O排放高峰出现最早,N处理排放速率最高(5.87 μg·kg^-1·h^-1);硝化抑制剂与脲酶抑制剂配施减少土壤N₂O排放的效果最佳。综合计算各处理直接N₂O和间接N₂O(NH₃)排放产生的温室效应潜能(GWP)发现,N+NI和NB+NI处理较N处理分别增加了34.8%和40.9%,而NB和NB+UI处理的GWP显著降低了45.9%和60.5%。因此,生物炭与脲酶抑制剂配施对降低土壤活性氮气体排放所产生的温室效应潜能效果最佳。     

Influence of COD/NH3–N ratio on organic removal and nitrification using a modified RBC

Synthetic wastewaters were prepared with different influent concentrations of ammonia nitrogen (NH₃–N) and COD and the treatment studies were conducted using a rotating biological contactor (RBC). If organic removal and nitrification can be simultaneously effected in one process, it will be an ideal solution to water pollution control. The RBC used in the present study was a four stage laboratory model and the discs were modified by attaching porous netlon sheets to enhance biofilm area. The COD loads (S ₀) used were about 1000 and 1500?mg/l whereas NH₃–N concentrations used were in the range of 20 to 185?mg/l. Hydraulic load (q) of 0.03?m³?.?m^-2?.?d^-1 and ammonia nitrogen loadings in the range of 0.66 to 5.5?g NH₃–N?.?m^-2?.?d^-1 were used. The RBC was operated at two different rotating speeds of 6 and 12?rpm. The results showed that the nitrification and percentage of COD removal were not affected up to the value of the COD/NH₃–N in the range from 47 to 23 at w=6?rpm and for an average influent COD of 1003?mg/l. Beyond that range only the nitrification rate decreased much whereas the percentage of COD removal was not affected. Similarly, at an influent COD load of 1557?mg/l, the nitrification and percentage COD removal were not affected for the value of the COD/NH₃–N in the range from 44 to 23 but beyond that range only the nitrification rate decreased while the percentage of COD removal was approximately constant and still high. A correlation plot between the NH₃–N removed and NH₃–N applied was presented at a rotating speed of 6?rpm and it was found that the nitrification rate of 3.93?g NH₃–N?.?m^-2?.?d^-1 was achieved at ammonia loading of 5.55?g NH₃–N?.?m^-2?.?d^-1. Also the results at w=12?rpm showed improvement of nitrification rate over those at 6?rpm.     

Evaluation of thiosulfate as a nitrification inhibitor for manures and fertilizers

Nitrogen from poultry manure (PM) and ammoniacal fertilizers undergoes rapid nitrification upon addition to soils, making it highly susceptible to leaching and thus creating a potential for groundwater contamination by nitrate-N. Any management technique that could delay nitrification would be desirable. A laboratory incubation study was conducted to determine the effect of thiosulfate, a known nitrification inhibitor, on nitrification in a loamy sand soil amended with five N sources, including two poultry manures and three N fertilizers [(NH₄)₂SO₄, NH₄NO₃, CO(NH₂)₂]. The manures or fertilizers were added to a soil-sand mixture alone or in combination with Na₂S₂O at a rate of 100 mg N kg^-1 for the inorganic N sources and 147 mg N kg^-1 and 122 mg N kg^-1 for PM-1 and PM-2 respectively. All treatments were incubated for 12 weeks and analyzed periodically for NO₃-N and NH₄-N.Thiosulfate was most effective with NH₄NO₃, maintaining 100% inhibition of nitrification throughout the 12 week study, and with (NH₄)₂SO₄ (89% inhibition at 12 weeks). Thiosulfate also inhibited nitrification from urea and poultry manure, but the inhibitory effect diminished later in the incubation. Urea had 81% inhibition of nitrification after eight weeks, decreasing to 26% by week 12, while the manures averaged 89% inhibition after four weeks and 20% at week 12. Net mineralization of organic N from PM was also reduced by the use of thiosulfate, particularly for PM-1 where the percentage of organic N mineralized decreased from 42% after four weeks incubation to 3% at week 12. Therefore, while thiosulfate can reduce nitrification from manures, and thus the potential for nitrate leaching, the timing of manure application will influence the effect of thiosulfate on the availability of manure N for plant uptake or leaching.     

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.     

Effect of nitrogen addition on Miscanthus × giganteus yield,nitrogen losses,and soil organic matter across five sites

The US Department of Energy has mandated the production of 16 billion gallons (60.6 billion liters) of renewable biofuel from cellulosic feedstocks by 2022. The perennial grass, Miscanthus × giganteus, is a potential candidate for cellulosic biofuel production because of high productivity with minimal inputs. This study determined the effect of three different spring fertilizer treatments (0, 60, and 120 kg N ha^?1 yr^?1 as urea) on biomass production, soil organic matter (SOM), and inorganic N leaching in Illinois, Kentucky, Nebraska, New Jersey, and Virginia, along with N₂O and CO₂ emissions at the IL site. There were no significant yield responses to fertilizer treatments, except at the IL site in 2012 (yields in 2012, year 4, varied from 10 to 23.7 Mg ha^?1 across all sites). Potentially mineralizable N increased across all fertilizer treatments and sites in the 0–10 cm soil depth. An increase in permanganate oxidizable carbon (POX‐C, labile C) in surface soils occurred at the IL and NJ sites, which were regularly tilled before planting. Decreases in POX‐C were observed in the 0 – 10 cm soil depth at the KY and NE sites where highly managed turfgrass was grown prior to planting. Growing M. × giganteus altered SOM composition in only 4 years of production by increasing the amount of potentially mineralizable N at every site, regardless of fertilization amount. Nitrogen applications increased N leaching and N₂O emission without increasing biomass production. This suggests that for the initial period (4 years) of M. × giganteus production, N application has a detrimental environmental impact without any yield benefits and thus should not be recommended. Further research is needed to define a time when N application to M. × giganteus results in increased biomass production.     

Low sedimentary accumulation of lead caused by weak downward export of organic matter in Hudson Bay,northern Canada

Subtropical forests receive increasing amounts of atmogenic nitrogen (N), both as ammonium (NH₄ ⁺) and nitrate (NO₃ ^?). Previous long-term studies indicate efficient turnover of atmogenic NH₄ ⁺ to NO₃ ^? in weathered, acidic soils of the subtropics, leading to excessive NO₃ ^? leaching. To clarify the mechanism governing the fate of atmogenic inputs in these soils, we conducted an in situ ¹⁵N tracing experiment in the TieShanPing (TSP) forested catchment, SW China. ¹⁵NH₄NO₃, NH ₄ ¹⁵ NO₃ and ¹⁵N-glutamic acid were applied to an upland hillslope soil and inorganic N, total soil N and nitrous oxide (N₂O) were monitored for nine days. Incorporation of ¹⁵NO₃ ^? into soil organic N was negligible and 80% of the applied label was lost from the top soil (0–15 cm) primarily by leaching within 9 days. In contrast, ¹⁵NH₄ ⁺ was largely retained in soil organic N. However, instant production of ¹⁵NO₃ ^? in the ¹⁵NH₄ ⁺ treatment suggested active nitrification. In both the ¹⁵NH₄ ⁺ and ¹⁵N-glutamic acid treatments, the ¹⁵N enrichment in the NO₃ ^? pool exceeded that in the NH₄ ⁺ pool one day after ¹⁵N application, suggesting preferential nitrification of added ¹⁵NH₄ ⁺ with subsequent dilution of the NH₄ ⁺ pool and/or immobilization of ¹⁵NH₄ ⁺ followed by heterotrophic nitrification. The cumulative recovery of ¹⁵N in N₂O after 9 days ranged from 2.5 to 6.0% in the ¹⁵NO₃ ^? treatment, confirming the previously reported significant response of N₂O emission to N deposition. Source partitioning of ¹⁵N₂O demonstrated a measurable contribution of nitrification to N₂O emissions, particularly at low soil moistures. Our study emphasizes the role of a fast-cycling organic N pool (including microbial N) for retention and transformation of atmogenic NH₄ ⁺ in subtropical, acid forest soils. Thus, it explains the near-quantitative leaching of deposited N (as NO₃ ^? and NH₄ ⁺) common to subtropical forest soils with chronic, elevated atmogenic N inputs by (i) negligible retention of NO₃ ^? in the soil and (ii) rapid immobilization-mineralization of NH₄ ⁺ followed by nitrification. Our findings point to a leaky N cycle in N-saturated Chinese subtropical forests with consequences for regional soil acidification, N pollution of fresh waters and N₂O emission.     

Transferring soils from high- to low-elevation forests increases nitrogen cycling rates: climate change implications

We assessed the potential impact of global warming resulting from a doubling of preindustrial atmospheric CO₂ on soil net N transformations by transferring intact soil cores (0–15 cm) from a high-elevation old-growth forest to a forest about 800 m lower in elevation in the central Oregon Cascade Mountains, USA. The lower elevation site had mean annual air and soil (10-cm mineral soil depth) temperatures about 2.4 and 3.9 °C higher than the high-elevation site, respectively. Annual rates of soil net N mineralization and nitrification more than doubled in soil transferred to the low-elevation site (17.2–36.0 kg N ha^–1 and 5.0–10.7 kg NO₃^––N ha^–1, respectively). Leaching of inorganic N from the surface soil (in the absence of plant uptake) also increased. The reciprocal treatment (transferring soil cores from the low- to the high-elevation site) resulted in decreases of about 70, 80, and 65% in annual rates of net N mineralization, nitrification, and inorganic N leaching, respectively. Laboratory incubations of soils under conditions of similar temperature and soil water potential suggest that the quality of soil organic matter is higher at the high-elevation site. Similar in situ rates of soil net N transformations between the two sites occurred because the lower temperature counteracts the effects of greater substrate quantity and quality at the high elevation site. Our results support the hypothesis that high-elevation, old-growth forest soils in the central Cascades have higher C and N storage than their low-elevation analogues primarily because low temperatures limit net C and N mineralization rates at higher elevations.     

Recovery of 15N-labeled urea and soil nitrogen dynamics as affected by irrigation management and nitrogen application rate in a double rice cropping system

A sophisticated soil microcosm system and ¹⁵N-labeled urea were used to investigate nitrogen (N) use efficiency and soil N dynamics in a rice monoculture system in two successive seasons. Topsoil (0 cm?C20 cm) and subsoil (20 cm?C50 cm) samples were collected from a traditional double rice cropping field in the Jiangxi Province, China, and these soil samples were derived from Quaternary red clay. Treatments were randomly assigned with two irrigation regimes and three N application rates (no application control, 80% traditional rate and 100% traditional rate noted as N0, N1 and N2, respectively). The levels of ¹⁵N recovery of plants, ¹⁵N and N remaining in soil were determined. Moreover, the N dynamic of soil solution from different layers of the soil profile was surveyed. The results showed that the effects of irrigation management and N application rate varied in different rice growing seasons. Irrigation regimes had remarkable effects on grain yield and chemical ¹⁵N fertilizers (CF-¹⁵N) uptake. When compared to flood irrigation (FI), the shallow water depth with wetting and drying (WD) increased grain yield up to 5.7%?C20%. Although the highest grain yield was obtained with reduced N application level, both N apparent recovery (NAR) and ¹⁵N use efficiency (the percentage of plant N uptake derived from applied N, %Ndfan) significantly decreased with increasing N inputs. However, the interaction between irrigation management and N application rate on grain yield and N use efficiency (NUE) of CF-¹⁵N were not significant. A survey of soil solutions every 5 days indicated that NH ₄ ⁺ -N was the main residual form of N, and high NH ₄ ⁺ -N leaching was observed. When compared to FI, WD decreased vertical NH ₄ ⁺ -N and TN leaching, especially at 10?C50 cm depths of soil profile in the second season. NH ₄ ⁺ -N was the main N residual form in the soil profile. Therefore, in this study, the WD irrigation regime and reduced rate (N1) was the optimal irrigation and fertilizer management strategy to increase the NUE of CF-N, increase the after effects of CF-¹⁵N, decrease leaching loss of CF-¹⁵N and minimize the shallow groundwater pollution risk, which were all beneficial for the ecological environment.