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.     

Soil Solution Nitrogen Losses During Clearing of Lowland Amazon Forest for Pasture

Losses of nitrogen (N) often follow severe disturbance of forest ecosystems. In tropical forests, losses of N associated with the disturbance of clearing may be particularly important because rates of soil N cycling are high and forest clearing now occurs on a large scale. We measured soil solution inorganic N concentrations and fluxes for 1 year in an intact forest in the Brazilian Amazon state of Rondônia and in an adjacent 3-ha forest plot that was cleared for pasture by cutting, burning and planting pasture grass and in established cattle pastures on the same soils that were 5 and 22 years old. The cleared forest had higher soil solution NO ₃ ^? concentrations than the intact forest, but the difference between the cleared and control forests declined with time after the start of the first post-clearing rainy season. Established pastures had much lower solution NH ₄ ⁺ and NO ₃ ^? concentrations than forest or cleared forest. Estimated annual dissolved inorganic solution N fluxes to below 1 m during the first year after clearing were 2.5 kg ha^?1 in forest and 24.4 kg ha^?1 in newly cleared forest compared with only 0.5–1.2 kg ha^?1 in established pastures. The solution fluxes from cleared forest during the first year after clearing were approximately 7 times greater than gaseous N oxide (N₂O+NO) losses estimated for the same time. These results were consistent with the characterization of moist tropical forests on weathered soils as N-rich and likely to respond to disturbances that elevate soil N availability with increased loss to both soil solution and the atmosphere. These results also suggest that the relative increase in N oxide loss is substantially less than the increase solution inorganic N loss.     

Quantifying the contribution of land use to N<Subscript>2</Subscript>O,NO and CO<Subscript>2</Subscript> fluxes in a montane forest ecosystem of Kenya

Increasing demand for food and fibre by the growing human population is driving significant land use (LU) change from forest into intensively managed land systems in tropical areas. But empirical evidence on the extent to which such changes affect the soil-atmosphere exchange of trace gases is still scarce, especially in Africa. We investigated the effect of LU on soil trace gas production in the Mau Forest Complex region, Kenya. Intact soil cores were taken from natural forest, commercial and smallholder tea plantations, eucalyptus plantations and grazing lands, and were incubated in the lab under different soil moisture conditions. Soil fluxes of nitrous oxide (N₂O), nitric oxide (NO) and carbon dioxide (CO₂) were quantified, and we approximated annual estimates of soil N₂O and NO fluxes using soil moisture values measured in situ. Forest and eucalyptus plantations yielded annual fluxes of 0.3–1.3 kg N₂O–N ha^?1 a^?1 and 1.5–5.2 kg NO–N ha^?1 a^?1. Soils of commercial tea plantations, which are highly fertilized, showed higher fluxes (0.9 kg N₂O–N ha^?1 a^?1 and 4.3 kg NO–N ha^?1 a^?1) than smallholder tea plantations (0.1 kg N₂O–N ha^?1 a^?1 and 2.1 kg NO–N ha^?1 a^?1) or grazing land (0.1 kg N₂O–N ha^?1 a^?1 and 1.1 kg NO–N ha^?1 a^?1). High soil NO fluxes were probably the consequence of long-term N fertilization and associated soil acidification, likely promoting chemodenitrification. Our experimental approach can be implemented in understudied regions, with the potential to increase the amount of information on production and consumption of trace gases from soils.     

Atmospheric nitrogen inputs and losses along an urbanization gradient from Boston to Harvard Forest,MA

Urbanization alters nitrogen (N) cycling, but the spatiotemporal distribution and impact of these alterations on ecosystems are not well-quantified. We measured atmospheric inorganic N inputs and soil leaching losses along an urbanization gradient from Boston, MA to Harvard Forest in Petersham, MA. Atmospheric N inputs at urban sites (12.3 ± 1.5 kg N ha^?1 year^?1) were significantly greater than non-urban (5.7 ± 0.5 kg N ha^?1 year^?1) sites with NH₄ ⁺ (median value of 77 ± 4 %) contributing thrice as much as NO₃ ^?. Proximity to urban core correlated positively with NH₄ ⁺ (R² = 0.57, p = 0.02) and total inorganic N inputs (R² = 0.61, p = 0.01); on-road CO₂ emissions correlated positively with NO ₃ ^? inputs (R² = 0.74, p = 0.003). Inorganic N leaching rates correlated positively with atmospheric N input rates (R² = 0.61, p = 0.01), but did not differ significantly between urban and non-urban sites (p > 0.05). Our empirical measurements of atmospheric N inputs are greater for urban areas and less for rural areas compared to modeled regional estimates of N deposition. Five of the nine sites had NO ₃ ^? leached that came almost entirely from nitrification, indicating that the NO₃ ^? in leachate came from biological processes rather than directly passing through the soil. A significant proportion (17–100 %) of NO ₃ ^? leached from the other four sites came directly from the atmosphere. Surprisingly, the four sites where atmospheric sources made up the largest proportion of leachate NO₃ ^? also had relatively low N leaching rates, suggesting that atmospheric N inputs added to terrestrial ecosystems can move to multiple sinks and losses simultaneously, rather than being lost via leaching only after abiotic and biotic sinks have become saturated. This study improves our understanding of atmospheric N deposition and leaching in urban ecosystems, and highlights the need to incorporate urbanization effects in N deposition models.     

Plant and soil responses of an alpine steppe on the Tibetan Plateau to multi-level nitrogen addition

Background

Although plant growth in alpine steppes on the Tibetan Plateau has been suggested to be sensitive to nitrogen (N) addition, the N limitation conditions of alpine steppes remain uncertain.

Methods

After 2 years of fertilization with NH₄NO₃ at six rates (0, 10, 20, 40, 80 and 160 kg N ha^?1 yr^?1), the responses of plant and soil parameters as well as N₂O fluxes were measured.

Results

At the vegetation level, N addition resulted in an increase in the aboveground N pool from 0.5?±?0.1 g m^?2 in the control plots to 1.9?±?0.2 g m^?2 in the plots at the highest N input rate. The aboveground C pool, biomass N concentration, foliar δ¹⁵N, soil NO₃ ^?-N and N₂O flux were also increased by N addition. However, as the N fertilization rate increased from 10 kg N ha^?1 yr^?1 to 160 kg N ha^?1 yr^?1, the N-use efficiency decreased from 12.3?±?4.6 kg C kg N^?1 to 1.6?±?0.2 kg C kg N^?1, and the N-uptake efficiency decreased from 43.2?±?9.7 % to 9.1?±?1.1 %. Biomass N:P ratios increased from 14.4?±?2.6 in the control plots to 20.5?±?0.8 in the plots with the highest N input rate. Biomass N:P ratios, N-uptake efficiency and N-use efficiency flattened out at 40 kg N ha^?1 yr^?1. Above this level, soil NO₃ ^?-N began to accumulate. The seasonal average N₂O flux of growing season nonlinearly increased with increased N fertilization rate and linearly increased with the weighted average foliar δ¹⁵N. At the species level, N uptake responses to relative N availability were species-specific. Biomass N concentration of seven out of the eight non-legume species increased significantly with N fertilization rates, while Kobresia macrantha and the one legume species (Oxytropics glacialis) remained stable. Both the non-legume and the legume species showed significant ¹⁵N enrichment with increasing N fertilization rate. All non-legume species showed significant increased N:P ratios with increased N fertilization rate, but not the legume species.

Conclusions

Our findings suggest that the Tibetan alpine steppes might be N-saturated above a critical N load of 40 kg N ha^?1 yr^?1. For the entire Tibetan Plateau (ca. 2.57 million km²), a low N deposition rate (10 kg N ha^?1 yr^?1) could enhance plant growth, and stimulate aboveground N and C storage by at least 1.1?±?0.3 Tg N yr^?1 and 31.5?±?11.8 Tg C yr^?1, respectively. The non-legume species was N-limited, but the legume species was not limited by N.     

Impact of DOC trends resulting from changing climatic extremes and atmospheric deposition chemistry on periphyton community of a freshwater tropical lake of India

Recent measurements have demonstrated unprecedented increase in atmospheric deposition of nutrients in many parts of India. To determine whether atmospheric nutrient inputs would increase phytoplankton growth and catchment dissolved organic carbon (DOC) flushing to constrain benthic algae, we analyzed NO₃ ^? and PO ₄ ^?3 in atmospheric deposits; nutrients and DOC in runoff and lake water and standing crop biomass of phytoplankton and periphyton at Jaisamand Lake of Rajasthan, India. Atmospheric deposition of NO₃ ^? (7.18–29.95 kg ha^?1 year^?1) and PO ₄ ^?3 (0.56–2.15 kg ha^?1 year^?1) showed a consistently rising trend across the year. Microbial biomass and activity in catchment increased in response to atmospheric deposition. Lake DOC and nutrients showed strong coherence with their terrestrial and atmospheric fluxes. Phytoplankton development showed significant linearity with atmospheric input of nutrients. Air-driven input appeared to have compensated the nutrient constraints to phytoplankton during drought. The N:P stoichiometry of deposition and that of lake water indicated that, although there was a seasonal switchover to N- or P-limitation, phytoplankton were mainly co-limited by N and P due probably to the synergistic effects of combined N + P enrichment in the pelagic zone of the lake. Periphyton standing crop showed inverse relationship with phytoplankton and lake DOC. The study indicated that enhanced phytoplankton development and terrestrial DOC flushing in response to atmospheric nutrient input attenuated light penetration to constrain algal periphyton. We suggests that data on these issues may be considered in developing aquatic ecosystem models to establish future links between changing air–water–land interactions and associated shifts in lake ecosystem functioning for more accurately predicting climate change drivers and designing integrated lake basin management strategies.     

Responses of nitrous oxide fluxes and soil nitrogen cycling to nutrient additions in montane forests along an elevation gradient in southern Ecuador

Tropical montane forests are commonly limited by N or co-limited by N and P. Projected increases in N deposition in tropical montane regions are thought to be insufficient for vegetation demand and are not therefore expected to affect soil N availability and N₂O emissions. We established a factorial N- and P-addition experiment (i.e., N, P, N + P, and control) across an elevation gradient of montane forests in Ecuador to test these hypotheses: (1) moderate rates of N and P additions are able to stimulate soil-N cycling rates and N₂O fluxes, and (2) the magnitude and timing of soil N₂O-flux responses depend on the initial nutrient status of the forest soils. Moderate rates of nutrients were added: 50 kg N ha^?1 year^?1 (in the form of urea) and 10 kg P ha^?1 year^?1 (in the form of NaH₂PO ₄ ^. 2H₂O) split in two equal applications. We tested the hypotheses by measuring changes in net rates of soil–N cycling and N₂O fluxes during the first 2 years (2008–2009) of nutrient manipulation in an old-growth premontane forest at 1,000 m, growing on a Cambisol soil with no organic layer, in an old-growth lower montane forest at 2,000 m, growing on a Cambisol soil with an organic layer, and an old-growth upper montane rainforest at 3,000 m, growing on a Histosol soil with a thick organic layer. Among the control plots, net nitrification rates were largest at the 1,000-m site whereas net nitrification was not detectable at the 2,000- and 3,000-m sites. The already large net nitrification at the 1,000-m site was not affected by nutrient additions, but net nitrification became detectable at the 2,000- and 3000-m sites after the second year of N and N + P additions. N₂O emissions increased rapidly following N and N + P additions at the 1,000-m site whereas only smaller increases occurred at the 2,000- and 3,000-m sites during the second year of N and N + P additions. Addition of P alone had no effect on net rates of soil N cycling and N₂O fluxes at any elevation. Our results showed that the initial soil N status, which may also be influenced by presence or absence of organic layer, soil moisture and temperature as encompassed by the elevation gradient, is a good indicator of how soil N cycling and N₂O fluxes may respond to future increases in nutrient additions.     

Threshold responses of soil organic carbon concentration and composition to multi-level nitrogen addition in a temperate needle-broadleaved forest

Responses of soil organic carbon (SOC) cycling and C budget in forest ecosystems to elevated nitrogen (N) deposition are divergent. Little is known about the N critical loads for the shift between gain and loss of SOC storage in the old-growth temperate forest of Northeast China. The objective of this study was to investigate the nonlinear responses of SOC concentration and composition to multiple rates of N addition, as well as the microbial mechanisms responsible for SOC alteration under N enrichment. Nine rates of urea addition (0, 10, 20, 40, 60, 80, 100, 120, 140 kg N ha^?1 year^?1) with 4 replicates for each treatment were conducted. Soil samples in the 0–10 cm mineral layer were taken after 3 years of N fertilization. Soil aggregate size distribution and SOC physical fractionation were performed to examine SOC dynamics. Phospholipid fatty acid (PLFA) technique was used to measure the abundance and structure of microbial community. Three years of N addition led to significant increases in the concentrations of soil particulate organic C and aggregate-associated organic C fractions only. The responses of total N and each labile SOC fraction to the rates of N addition followed Gaussian equations, with the N critical loads being estimated to be between 80 and 100 kg N ha^?1 year^?1. The change in SOC concentration (ΔSOC) was positively correlated with the changes in aggregate associated OC (r² > 0.80) and POC concentrations (r² > 0.50). Significant correlations among the concentrations of labile SOC fractions, the percentages of soil aggregates, and the abundances of microbial PLFAs were observed, which implies a close linkage between microbial community structure and SOC accumulation and stability. Our results suggest that increase in soil moisture and shift of microbial community structure could control the critical N load for the switch between C accumulation and loss. The current N deposition rate (~ 11 kg N ha^?1 year^?1) to the northeast China’s forests is favorable for soil C accumulation over the short term.     

The effect of nitrogen addition on soil organic matter dynamics: a model analysis of the Harvard Forest Chronic Nitrogen Amendment Study and soil carbon response to anthropogenic N deposition

Recent observations indicate that long-term N additions can slow decomposition, leading to C accumulation in soils, but this process has received limited consideration by models. To address this, we developed a model of soil organic matter (SOM) dynamics to be used with the PnET model and applied it to simulate N addition effects on soil organic carbon (SOC) stocks. We developed the model’s SOC turnover times and responses to experimental N additions using measurements from the Harvard Forest, Massachusetts. We compared model outcomes to SOC stocks measured during the 20th year of the Harvard Forest Chronic Nitrogen Amendment Study, which includes control, low (5 g N m^?2 yr^?1) and high (15 g N m^?2 yr^?1) N addition to hardwood and red pine stands. For unfertilized stands, simulated SOC stocks were within 10 % of measurements. Simulations that used measured changes in decomposition rates in response to N accurately captured SOC stocks in the hardwood low N and pine high N treatment, but greatly underestimated SOC stocks in the hardwood high N and the pine low N treatments. Simulated total SOC response to experimental N addition resulted in accumulation of 5.3–7.9 kg C per kg N following N addition at 5 g N m^?2 yr^?1 and 4.1–5.3 kg C per kg N following N addition at 15 g N m^?2 yr^?1. Model simulations suggested that ambient atmospheric N deposition at the Harvard Forest (currently 0.8 g N m^?2 yr^?1) has led to an increase in cumulative O, A, and B horizons C stocks of 211 g C m^?2 (3.9 kg C per kg N) and 114 g C m^?2 (2.1 kg C per kg N) for hardwood and pine stands, respectively. Simulated SOC accumulation is primarily driven by the modeled decrease in SOM decomposition in the Oa horizon.     

Application of nitrogen in NO 3 − form increases rhizosphere alkalisation in the subsurface soil layers in an acid soil

Leaching of NO ₃ ^? derived from ammoniacal fertilizers in the topsoil and subsequent uptake of NO ₃ ^? by plants from deeper layers may be used as a method of biological amelioration of subsurface soil acidity. This paper reports a glasshouse column experiment testing the above concept. Nitrogen with labelled ¹⁵N was supplied with and without lime to the surface soil (0–10 cm) as urea, (NH₄)₂SO₄ or Ca(NO₃)₂ at a rate equivalent to 120 kg N ha^?1. Soil columns were regularly watered from the top to facilitate NO ₃ ^? leaching. An aluminium-tolerant wheat genotype was grown for 38 days. The application of lime with nitrogen fertilizers increased growth of shoot and roots in all soil layers. The application of Ca(NO₃)₂ resulted in about 66% of recovery efficiency irrespective of whether lime was applied in the surface. This in turn resulted in about 0.2 units increase in rhizosphere pH in the subsurface (10–15 cm) soil layer compared to the same layer of the unlimed control. The supply of urea and (NH₄)₂SO₄ alone or with lime did not increase rhizosphere pH in the subsurface soil layers. Importantly, this study indicates that it is possible to exploit the process of nitrate uptake by wheat to increase pH in acidic subsurface soil.     

Nitrogen contributions from faba bean (Vicia faba L.) reliant on soil rhizobia or inoculation

Background and Aims

Understanding the impact of soil rhizobial populations and inoculant rhizobia in supplying sufficient nodulation is crucial to optimising N₂ fixation by legume crops. This study explored the impact of different rates of inoculant rhizobia and contrasting soil rhizobia on nodulation and N₂ fixation in faba bean (Vicia faba L.).

Methods

Faba beans were inoculated with one of seven rates of rhizobial inoculation, from no inoculant to 100 times the normal rate of inoculation, sown at two field sites, with or without soil rhizobia present, and their nodulation and N₂ fixation assessed.

Results

At the site without soil rhizobia, inoculation increased nodule number and increased N₂ fixation from 21 to 129 kg shoot N ha^?1, while N₂ fixation increased from 132 to 218 kg shoot N ha^?1 at the site with high background soil rhizobia. At the site without soil rhizobia, inoculation increased concentrations of shoot N from 14 to 24 mg g^?1, grain N from 32 to 45 mg g^?1, and grain yields by 1.0 Mg (metric tonne) ha^?1. Differences in nodulation influenced the contributions of fixed N to the system, which varied from the net removal of 20 kg N ha^?1 from the system in the absence of rhizobia, to a net maximum input of 199 kg N ha^?1 from legume shoot and root residues, after accounting for removal of N in grain harvest.

Conclusions

The impact of inoculation and soil rhizobia strongly influenced grain yield, grain N concentration and the potential contributions of legume cropping to soil N fertility. In soil with resident rhizobia, N₂ fixation was improved only with the highest inoculation rate.     

Soil nitrogen balance resulting from N fixation and rhizodeposition by the symbiotic association Anthyllis vulneraria/Mesorhizobium metallidurans grown in highly polluted Zn,Pb and Cd mine tailings

Background and aims

The association of the legume Anthyllis vulneraria and the grass Festuca arvernensis, was found to be very efficient for the phytostabilisation of highly multi-metal contaminated mine tailings. Our objective was to quantify the contribution of Anthyllis inoculated with its symbiotic bacteria Mesorhizobium metallidurans to the soil N pool and to test whether a starter nitrogen fertilization may improve symbiotic nitrogen fixation and the growth of Festuca.

Methods

Plants of Festuca and of Anthyllis inoculated with M. metallidurans were grown separately during eight months in pots filled with mine contaminated soil. Estimation of the N fluxes was realized using ¹⁵?N isotopic methods.

Results

Starter N fertilization (28 kg N ha^?1) improved symbiotic N₂ fixation and the growth of both species. Belowground N balance (N rhizodeposition – soil N uptake) of the non-fertilized Anthyllis at maturity was negative (?30.6 kg N ha^?1). However, the amount of N derived from fixation, including above- and belowground parts, was 78.6 kg N ha^?1, demonstrating the ability of this symbiotic association to improve soil N content after senescence.

Conclusions

i) soil N enrichment by the N₂-fixing symbiotic association occurs after plant senescence, when decaying leaves and shoots are incorporated into the soil; ii) application of a starter fertilization is an efficient solution to improve phytostabilisation of highly contaminated sites.     

Nitrogen cycling in forest soils across climate gradients in Eastern China

A ¹⁵N tracing study was carried out to investigate the potential gross nitrogen (N) dynamics in thirteen forest soils in Eastern China ranging from temperate to tropical zones (five coniferous forests, six deciduous broad-leaf forests, one temperate mixed forest, one evergreen broad-leaf forests ecosystems), and to identify the major controlling factors on N cycling in these forest ecosystems. The soil pH ranged from 4.3 to 7.9 and soil organic carbon (SOC) ranged from 6.6 g?kg^?1 to 83.0 g?kg^?1. The potential gross N transformation rates were quantified by ¹⁵N tracing studies where either the ammonium or nitrate pools were ¹⁵N labeled in parallel treatments. Gross mineralization rates ranged from 0.915 μg N g^?1 soil day^?1 to 2.718 μg N g^?1 soil day^?1 in the studied forest soils. The average contribution of labile organic-N (M _Nlab ) to total gross mineralization (M _Nrec +M _Nlab ) was 86% (58% to 99%), indicating that turnover of labile organic N plays a dominant role in the studied forest ecosystems. The gross mineralization rates in coniferous forest soils were significantly lower (ranging between 0.915 and 1.228 μg N g^?1 soil day^?1) compared to broad-leaf forest soils (ranging from 1.621 to 2.718 μg N g^?1 soil day^?1) (p?<?0.01). Thus, the dominant vegetation may play an important role in regulating soil N mineralization. Nitrate production (nitrification) occurred via two pathways, oxidation of NH ₄ ⁺ and organic N the forest soils. Correlations with soil pH indicated that this is a key factor controlling the oxidation of NH ₄ ⁺ and organic N in theses forest ecosystems. NH ₄ ⁺ oxidation decreased with a decline in pH while organic N oxidation increased. The climatic conditions (e.g. moisture status) at the various sites governed the NO ₃ ^? -N consumption processes (dissimilatory NO ₃ ^? reduction to NH ₄ ⁺ (DNRA) or immobilization of NO ₃ ^? ). Total NO ₃ ^? consumption and the proportion of total NO ₃ ^? consumption to total NO ₃ ^? production decreased with an increase in the drought index of ecosystems, showing that strong interactions appear to exist between climatic condition (e.g. the drought index), N mineralization and the rate of DNRA. Interactions between vegetation, climatic conditions govern internal N cycling in these forests soils.     

Simulation of N2O emissions and nitrate leaching from plastic mulch radish cultivation with LandscapeDNDC

Radish is one of the major dry field crops in Asia commonly grown with plastic mulch and high rates of N fertilization, and potentially harming the environment due to N₂O emissions and nitrate leaching. Despite the widespread use of plastic mulch, biogeochemical models so far do not yet consider impacts of mulch on soil environmental conditions and biogeochemistry. In this study, we adapted and successfully tested the LandscapeDNDC model against field data by simulating crop growth, C and N turnover and associated N₂O emissions as well as nitrate leaching for radish cultivation with plastic mulch and in conjunction with different rates of N fertilization (465–765 kg N ha^?1 year^?1). Due to the sandy soil texture and monsoon climate, nitrate leaching with rates up to 350 kg N ha^?1 year^?1 was the dominant reason for overall low nitrogen use efficiency (32–43 %). Direct or indirect N₂O emissions (calculated from simulated nitrate leaching rates and IPCC EF_ind = 0.0075) ranged between 2 and 3 kg N ha^?1 year^?1, thus contributing an equal amount to total field emissions of about 5 kg N ha^?1 year^?1. Based on our results, emission factors for direct N₂O emissions ranged between 0.004 and 0.005. These values are only half of the IPCC default value (0.01), demonstrating the need of biogeochemical models for developing site and/or region specific EFs. Simulation results also revealed that changes in agricultural management by applying the fertilizer only to the rows would be an efficient mitigation strategy, effectively decreasing field nitrate leaching and N₂O emissions by 50–60 %.     

Niche-based assessment of contributions of legumes to the nitrogen economy of Western Kenya smallholder farms

Nitrogen (N) deficiency is a major constraint to the productivity of the African smallholder farming systems. Grain, green manure and forage legumes have the potential to improve the soil N fertility of smallholder farming systems through biological N₂-fixation. The N₂-fixation of bean (Phaseolus vulgaris), soyabean (Glycine max), groundnut (Arachis hypogaea), Lima bean (Phaseolus lunatus), lablab (Lablab purpureus), velvet bean (Mucuna pruriens), crotalaria (Crotalaria ochroleuca), jackbean (Canavalia ensiformis), desmodium (Desmodium uncinatum), stylo (Stylosanthes guianensis) and siratro (Macroptilium atropurpureum) was assessed using the ¹⁵N natural abundance method. The experiments were conducted at three sites in western Kenya, selected on an agro-ecological zone (AEZ) gradient defined by rainfall. On a relative scale, Museno represents high potential AEZ 1, Majengo medium potential AEZ 2 and Ndori low potential AEZ 3. Rainfall in the year of experimentation was highest in AEZ 2, followed by AEZ 1 and AEZ 3. Experimental fields were classified into high, medium and low fertility classes, to assess the influence of soil fertility on N₂-fixation performance. The legumes were planted with triple super phosphate (TSP) at 30 kg P ha^?1, with an extra soyabean plot planted without TSP (soyabean-P), to assess response to P, and no artificial inoculation was done. Legume grain yield, shoot N accumulation, %N derived from N₂-fixation, N₂-fixation and net N inputs differed significantly (P<0.01) with rainfall and soil fertility. Mean grain yield ranged from 0.86 Mg ha^?1, in AEZ 2, to 0.30 Mg ha^?1, in AEZ 3, and from 0.78 Mg ha^?1, in the high fertility field, to 0.48 Mg ha^?1, in the low fertility field. Shoot N accumulation ranged from a maximum of 486 kg N ha^?1 in AEZ 2, to a minimum of 10 kg N ha^?1 in AEZ 3. Based on shoot biomass estimates, the species fixed 25–90% of their N requirements in AEZ 2, 23–90% in AEZ 1, and 7–77% in AEZ 3. Mean N₂-fixation by green manure legumes ranged from 319 kg ha^?1 (velvet bean) in AEZ 2 to 29 kg ha^?1 (jackbean) in AEZ 3. For the forage legumes, mean N₂-fixation ranged from 97 kg N ha^?1 for desmodium in AEZ 2 to 39 kg N ha^?1 for siratro in AEZ 3, while for the grain legumes, the range was from 172 kg N ha^?1 for lablab in AEZ 1 to 3 kg N ha^?1 for soyabean-P in AEZ 3. Lablab and groundnut showed consistently greater N₂-fixation and net N inputs across agro-ecological and soil fertility gradients. The use of maize as reference crop resulted in lower N₂-fixation values than when broad-leaved weed plants were used. The results demonstrate differential contributions of the green manure, forage and grain legume species to soil fertility improvement in different biophysical niches in smallholder farming systems and suggest that appropriate selection is needed to match species with the niches and farmers’ needs.     

Growth and metabolism characteristics of anaerobic ammonium-oxidizing bacteria aggregates

The present study reported the growth and metabolism characteristics of anaerobic ammonium-oxidizing (anammox) bacteria aggregates in an expanded granular sludge bed (EGSB). The results showed that the anammox bacteria aggregates presented starvation, growth, and inhibition phase along with the increase of substrate supply. The substrate conversion rates for survival were 0.05 kgNH ₄ ⁺ –N/(kgVSS·day), 0.07 kgNO ₂ ^? –N/(kgVSS·day), and 0.12 kgN/(kgVSS·day); the substrate conversion rates for maximum growth were 0.21 kgNH ₄ ⁺ –N/(kgVSS·day), 0.24 kgNH ₄ ⁺ –N/(kgVSS·day), and 0.45 kgNH ₄ ⁺ –N/(kgVSS·day), respectively. In the growth phase, the yield of anammox bacteria aggregates was 0.14 gVSS/(gNH ₄ ⁺ –N), 0.12 gVSS/(gNO ₂ ^? –N), and 0.70 gVSS/(gNO ₃ ^? –N); the yield of extracellular polymeric substances (EPS) was 0.11 gEPS/(gNH ₄ ⁺ –N), 0.09 gEPS/(gNO ₂ ^? –N), and 0.55 gEPS/(gNO ₃ ^? –N), respectively. The EPS contents in anammox bacteria aggregates were high compared to that in anaerobic granular sludge. Speculated from the cell yield, the energy for anammox bacteria growth was not only from nitrite oxidation, but also from anammox reaction.     

Nitrous oxide emissions during the non-rice growing seasons of two subtropical rice-based rotation systems in southwest China

Background and aims

High nitrous oxide (N₂O) emissions may occur during the non-rice growing season of Chinese rice-upland crop rotation systems. However, our understanding of N₂O emission during this season is poor due to a scarcity of available field N₂O measurements.

Methods

Using the static manual chamber-GC technique, seasonal N₂O emissions during the non-rice growing season were simultaneously measured at two adjacent rice-wheat and rice-rapeseed fields in southwest China for three consecutive annual rotation cycles (May 2005 to May 2008).

Results

Compared to the control, N fertilizer applications significantly enhanced soil N₂O emissions from both wheat and rapeseed systems. Seasonal cumulative N₂O fluxes from wheat systems were on average 2.6 kg N ha^?1 for the recommended practice (RP [150 kg N ha^?1]) and 5.0 kg N ha^?1 for the conventional practice (CP [250 kg N ha^?1]). Lower N₂O emissions were observed from the adjacent rapeseed systems. Average cumulative seasonal N₂O fluxes from rapeseed were 1.5 and 2.2 kg N ha^?1 for the RP and CP treatments, respectively. The first 3 weeks after N fertilization were the “hot moment” of N₂O emissions for both the wheat and rapeseed systems. The lowest yield-scaled N₂O fluxes for wheat were obtained at the RP treatment (mean: 0.81 kg N Mg^?1) while for rapeseed the CP treatment produced the lowest yield-scaled fluxes (mean: 0.79 kg N Mg^?1). On average, the direct N₂O emission factors (EF_d) for the wheat system (1.76 %) were over two times higher than for the rapeseed system (0.73 %).

Conclusions

Intercropping of rapeseed tends to result in lower N₂O emissions than wheat for rice-upland crop rotation systems of southwest China, indicating that either the N fertilization or the cropping system need to be considered not only for improving the estimate of regional and/or national N₂O fluxes but also for proposing the climate-smart agricultural management practice to reduce N₂O emissions from agricultural soils.     

Microbial N turnover processes in three forest soil layers following clear cutting of an N saturated mature spruce stand

Microbial N turnover processes were investigated in three different forest soil layers [organic (O) layer, 0–10 cm depth (M₁), 10–40 cm depth (M₂)] after the clear cutting of a nitrogen (N) saturated spruce stand at the Höglwald Forest (Bavaria, Germany). The aim of the study was to provide detailed insight into soil-layer specific microbial production and the consumption of inorganic N within the main rooting zone. Furthermore, we intended to clarify the relevance of each soil layer investigated in respect of the observed high spatial variation of seepage water nitrate (NO ₃ ^? ) concentration at a depth of 40 cm. The buried bag and the ¹⁵N pool dilution techniques were applied to determine the net and gross N turnover rates. In addition, soil pH, C:N ratio, pool sizes of soil ammonium (NH ₄ ⁺ ) and NO ₃ ^? , as well as quantities of microbial biomass carbon (C_mic) and nitrogen (N_mic) were determined. The 40 cm thick upper mineral soil was found to be the main place of NO ₃ ^? production with a NO ₃ ^? supply or net nitrification three times higher than in the considerably thinner O layer. Nevertheless, O layer nitrification processes determined via in situ field experiments showed significant correlation with seepage water NO ₃ ^? . An improved correlation noted several months after the cut may result from a transport-induced time shift of NO ₃ ^? with downstream hydrological pathways. In contrast, the soil laboratory incubation experiments found no indication that mineral soil is relevant for the spatial heterogeneity of seepage water NO ₃ ^? . The results from our study imply that in situ experiments may be better suited to studies investigating N turnover in relation to NO ₃ ^? loss via seepage water in similar ecosystems in order to gain representative data.     

Modeling denitrification in a tile-drained, corn and soybean agroecosystem of Illinois, USA

Denitrification is known as an important pathway for nitrate loss in agroecosystems. It is important to estimate denitrification fluxes to close field and watershed N mass balances, determine greenhouse gas emissions (N₂O), and help constrain estimates of other major N fluxes (e.g., nitrate leaching, mineralization, nitrification). We compared predicted denitrification estimates for a typical corn and soybean agroecosystem on a tile drained Mollisol from five models (DAYCENT, SWAT, EPIC, DRAINMOD-N II and two versions of DNDC, 82a and 82h), after first calibrating each model to crop yields, water flux, and nitrate leaching. Known annual crop yields and daily flux values (water, nitrate-N) for 1993–2006 were provided, along with daily environmental variables (air temperature, precipitation) and soil characteristics. Measured denitrification fluxes were not available. Model output for 1997–2006 was then compared for a range of annual, monthly and daily fluxes. Each model was able to estimate corn and soybean yields accurately, and most did well in estimating riverine water and nitrate-N fluxes (1997–2006 mean measured nitrate-N loss 28 kg N ha^?1 year^?1, model range 21–28 kg N ha^?1 year^?1). Monthly patterns in observed riverine nitrate-N flux were generally reflected in model output (r ² values ranged from 0.51 to 0.76). Nitrogen fluxes that did not have corresponding measurements were quite variable across the models, including 10-year average denitrification estimates, ranging from 3.8 to 21 kg N ha^?1 year^?1 and substantial variability in simulated soybean N₂ fixation, N harvest, and the change in soil organic N pools. DNDC82a and DAYCENT gave comparatively low estimates of total denitrification flux (3.8 and 5.6 kg N ha^?1 year^?1, respectively) with similar patterns controlled primarily by moisture. DNDC82h predicted similar fluxes until 2003, when estimates were abruptly much greater. SWAT and DRAINMOD predicted larger denitrification fluxes (about 17–18 kg N ha^?1 year^?1) with monthly values that were similar. EPIC denitrification was intermediate between all models (11 kg N ha^?1 year^?1). Predicted daily fluxes during a high precipitation year (2002) varied considerably among models regardless of whether the models had comparable annual fluxes for the years. Some models predicted large denitrification fluxes for a few days, whereas others predicted large fluxes persisting for several weeks to months. Modeled denitrification fluxes were controlled mainly by soil moisture status and nitrate available to be denitrified, and the way denitrification in each model responded to moisture status greatly determined the flux. Because denitrification is dependent on the amount of nitrate available at any given time, modeled differences in other components of the N cycle (e.g., N₂ fixation, N harvest, change in soil N storage) no doubt led to differences in predicted denitrification. Model comparisons suggest our ability to accurately predict denitrification fluxes (without known values) from the dominant agroecosystem in the midwestern Illinois is quite uncertain at this time.     

Impacts of fertilizer practices on environmental risk of nitrate in semiarid farmlands in the Loess Plateau of China

The lack of understanding of nitrate dynamics in soil profiles of semiarid regions hampers the assessment of the environmental risks associated with nitrate. A long-term field experiment established in the Loess Plateau of Northwest China in 1984 was used to investigate the seasonal dynamics of water and nitrate contents in the soil profile (0–300 cm) under bare fallow and continuous winter wheat (Triticum aestivum L.) with various fertilizer treatments. For treatments without mineral N input (i.e., no fertilizer, farmyard manure alone, and with P fertilizer), the amount of nitrate accumulated in the soil profile (52–120 kg N ha^?1, the average for June, August, February and April) was significantly lower than that (292 kg N ha^?1) accumulated in the bare fallow treatment. A large amount of nitrate (1,065 kg N ha^?1) was found accumulated in the soil profile with the treatment applied with mineral N at a rate of 120 kg N ha^?1 year^?1 for 17 years (1984–2001) and this nitrate moved downward during the wet season (from August to February). Clearly, the amount of nitrate accumulated in the soil profiles, and its tendency of downward movement, appears to potentially be an environmental risk as it may reach groundwater. Fertilization as mineral N fertilizers coupled with FYM or P resulted in 50–70% less nitrate accumulation in the soil profiles than that using mineral N fertilizer alone, and therefore the environmental risk was reduced. It is proposed that a “break point” of nitrate distribution existed in the soil profiles, providing an indication of soil depth to which nitrate can transfer.