Applying slurry with different techniques in spring – which pathway does the nitrogen take?

Author(s):  
Caroline Buchen-Tschiskale ◽  
Heinz Flessa ◽  
Reinhard Well

<p>One of the most important measures to reduce ammonia (NH<sub>3</sub>) and nitrous oxide (N<sub>2</sub>O) fluxes from crop production is the adoption of low-emission application techniques for slurry. Application techniques may also impact dinitrogen (N<sub>2</sub>) emission, as they can influence denitrification activity by changing slurry and soil aeration (e.g. by injection techniques), nitrate formation (e.g. by adding nitrification inhibitors) and the pH value (e.g. by slurry acidification). However, measuring N<sub>2</sub> emissions and following pathways of slurry nitrogen (N) transformation under field conditions is still challenging.</p><p>Thus, we set up a field experiment using undisturbed soil cores with growing winter wheat as small lysimeters. Cattle slurry treatments include the following application techniques: trailing hose with and without acidification (H<sub>2</sub>SO<sub>4</sub>), slot injection with and without nitrification inhibitor (DMPP). Soil cores without slurry application were used as control. In a first step, soil nitrate was <sup>15</sup>N labelled by homogeneous injection of a K<sup>15</sup>NO<sub>3</sub> solution (98 at% <sup>15</sup>N, equal to 4 kg N ha<sup>-1</sup>). One week later, we applied 72 kg N ha<sup>-1</sup><sup>15</sup>N-labelled slurry (NH<sub>4</sub><sup>+</sup> labelled at 65 at% <sup>15</sup>N). NH<sub>3</sub> emissions were measured by Dräger-Tube method (Pacholski, 2016). N<sub>2</sub>O and N<sub>2</sub> emission were measured using the <sup>15</sup>N gas flux method with N<sub>2</sub>-depleted atmosphere (Well et al., 2018). To close the N balance and follow the different N transformation pathways, <sup>15</sup>N losses by leaching, <sup>15</sup>N uptake by plant and residual <sup>15</sup>N in roots, plant residues, microbial biomass and soil were analysed by IRMS.</p><p>N<sub>2</sub>O emission were very low (up to 0.1 kg N<sub>2</sub>O-N ha<sup>-1</sup>) and not significantly different between treatments during the experimental period of 60 days. Since the N<sub>2</sub>O/(N<sub>2</sub>+N<sub>2</sub>O) ratio of denitrification (N<sub>2</sub>Oi) was also very low, most labelled N was lost via N<sub>2</sub> (up to 3 kg N ha<sup>-1</sup>). Nevertheless, the major gaseous loss pathway was NH<sub>3</sub> with up to 8 kg N ha<sup>-1</sup> in the trailing hose treatment. Slot injection significantly reduced NH<sub>3</sub> emission, while N leaching losses were up 5 kg N ha<sup>-1</sup>. Recovery of <sup>15</sup>N was higher in the soil N pool (32-48 %) than in plants (19-37 %) and roots (5-7 %). Total <sup>15</sup>N recovery was almost complete, indicating that the experiment was able to catch the relevant N pathways.</p><p><strong>References:</strong></p><p>Pacholski, A., 2016. Calibrated passive sampling-multi-plot field measurements of NH<sub>3</sub> emissions with a combination of dynamic tube method and passive samplers. Journal of visualized experiments: JoVE 109, e53273.</p><p>Well, R., Burkart, S., Giesemann, A., Grosz, B., Köster, J., Lewicka-Szczebak, D., 2018. Improvement of the <sup>15</sup>N gas flux method for in situ measurement of soil denitrification and its product stoichiometry. Rapid Communications in Mass Spectrometry 33, 437–448.</p>

2019 ◽  
Author(s):  
Dominika Lewicka-Szczebak ◽  
Reinhard Well

Abstract. 15N gas flux method allows for quantification of N2 flux and tracing soil N transformations. An important requirement for this method is a homogeneous distribution of the 15N tracer added to soil. This is usually achieved by soil homogenization and admixture of the 15N tracer solution or multipoint injection of tracer solution to intact soil. Both methods may create artefacts. We aimed at comparing the results of the gas flux method using both tracer distribution approaches. Intact soil cores with injected 15N tracer solution show wider range of the results obtained. Homogenized soil shows better agreement between repetitions, but significant differences in 15N enrichment measured in soil nitrate and in emitted gases were also observed. For intact soil the wider variability of measured values rather results from natural diversity of non-homogenized soil cores than from inhomogeneous label distribution. Generally, comparison of the results of intact cores and homogenized soil did not reveal statistically significant differences in N2 flux determination. In both cases, pronounced dominance of N2 flux over N2O flux was noted. It can be concluded that both methods showed close agreement and homogenized soil is not necessarily characterized by more homogenous 15N label distribution.


SOIL ◽  
2020 ◽  
Vol 6 (1) ◽  
pp. 145-152 ◽  
Author(s):  
Dominika Lewicka-Szczebak ◽  
Reinhard Well

Abstract. The 15N gas-flux method allows for the quantification of N2 flux and tracing soil N transformations. An important requirement for this method is a homogeneous distribution of the 15N tracer added to soil. This is usually achieved through soil homogenization and admixture of the 15N tracer solution or multipoint injection of tracer solution to intact soil. Both methods may create artefacts. We aimed at comparing the N2 flux determined by the gas-flux method using both tracer distribution approaches. Soil incubation experiments with silt loam soil using (i) intact soil cores injected with 15N label solution, (ii) homogenized soil with injected label solution, and (iii) homogenized soil with admixture of label solution were performed. Intact soil cores with injected 15N tracer solution show a larger variability of the results. Homogenized soil shows better agreement between repetitions, but significant differences in 15N enrichment measured in soil nitrate and in emitted gases were observed. For intact soil, the larger variability of measured values results rather from natural diversity of non-homogenized soil cores than from inhomogeneous label distribution. Generally, comparison of the results of intact cores and homogenized soil did not reveal statistically significant differences in N2 flux determination. In both cases, a pronounced dominance of N2 flux over N2O flux was noted. It can be concluded that both methods showed close agreement, and homogenized soil is not necessarily characterized by more homogenous 15N label distribution.


Agronomie ◽  
2000 ◽  
Vol 20 (3) ◽  
pp. 297-307 ◽  
Author(s):  
Pierre Benoit ◽  
Enrique Barriuso ◽  
Philippe Vidon ◽  
Benoit Réal

2018 ◽  
Vol 50 (1) ◽  
pp. 77-92 ◽  
Author(s):  
Kenneth Miller ◽  
Brenna J. Aegerter ◽  
Nicholas E. Clark ◽  
Michelle Leinfelder-Miles ◽  
Eugene M. Miyao ◽  
...  

2019 ◽  
Vol 33 (5) ◽  
pp. 437-448 ◽  
Author(s):  
Reinhard Well ◽  
Stefan Burkart ◽  
Anette Giesemann ◽  
Balázs Grosz ◽  
Jan Reent Köster ◽  
...  

1994 ◽  
Vol 74 (1) ◽  
pp. 99-107 ◽  
Author(s):  
D. C. Jans-Hammermeister ◽  
W. B. McGill ◽  
T. L. Jensen

The distribution and dynamics of 15N following green manuring of 15N-labelled 10% bloom and full bloom field pea (Pisum sativum ’Sirius’) were investigated in the soil mineral N, microbial N and non-microbial organic N (NMO-N) fractions and in a subsequent barley crop at two contrasting field sites in central Alberta: one on a Chernozemic (Dark Brown) soil near Provost and the other on a Luvisolic (Gray Luvisol) soil near Rimbey. Soils and plants were sampled four times during a 1-yr period. The 10% bloom and full bloom pea shoots were similar in dry matter production and N and C content. More N was, however, released from the younger pea residues directly following soil incorporation, which we attributed to a larger proportion of labile components. Barley yield, N content and 15N recovery in the grain were not influenced by legume bloom stage at incorporation, although significantly more 15N was recovered in the barley straw and roots of the full bloom treatment. Incorporation of full bloom legumes resulted in closer synchrony between the appearance of legume-derived mineral 15N and early N demand by the barley crop. The decay rate constants for the recalcitrant fraction of the legume residues were not significantly influenced by bloom stage or site over the time intervals of our observations and are, thus, consistent with the theory that decomposition of the recalcitrant fraction of plant residues can be described by a single exponential equation. Key words:15N, legume green manuring, Pisum sativum, decomposition


1986 ◽  
Vol 16 (1) ◽  
pp. 136-142 ◽  
Author(s):  
George A. Schier

The effects of simulated acid rain solutions on growth of pitch pine (Pinusrigida Mill.) seedlings in undisturbed soil cores from the New Jersey Pine Barrens were examined. Solutions of pH 5.6, 4.0, and 3.0 (SO42−–Cl−–NO3−, 4:2:1), totaling 1.4 times annual ambient precipitation, were applied directly to soil cores from the A horizon during a 1-year period. By varying photoperiod and diurnal temperature, two growing "seasons" with an intervening dormant period were simulated. Soil chemistry, soil leachate chemistry, seedling nutrition, and seedling growth were monitored. Seedling dry weight was significantly greater at pH 3.0 than at the less acid treatments. Foliar nutrient contents indicated that growth stimulation at pH 3.0 probably resulted because of increased availability of nitrogen and input of nutrient cations from acid-induced weathering of soil minerals. There were sharp increases in Ca and Mg leaching when the pH of the irrigating solution was lowered, but solution acidity had little effect on depletion of K. Declines in nutrient leaching during the experiment indicated that weatherable cations were becoming depleted. Although Al mobility was greatly accelerated by an increase in acid inputs, Al toxicity symptoms were not observed.


2019 ◽  
Vol 16 (10) ◽  
pp. 2233-2246 ◽  
Author(s):  
Reinhard Well ◽  
Martin Maier ◽  
Dominika Lewicka-Szczebak ◽  
Jan-Reent Köster ◽  
Nicolas Ruoss

Abstract. Common methods for measuring soil denitrification in situ include monitoring the accumulation of 15N-labelled N2 and N2O evolved from 15N-labelled soil nitrate pool in closed chambers that are placed on the soil surface. Gas diffusion is considered to be the main transport process in the soil. Because accumulation of gases within the chamber decreases concentration gradients between soil and the chamber over time, the surface efflux of gases decreases as well, and gas production rates are underestimated if calculated from chamber concentrations without consideration of this mechanism. Moreover, concentration gradients to the non-labelled subsoil exist, inevitably causing downward diffusion of 15N-labelled denitrification products. A numerical 3-D model for simulating gas diffusion in soil was used in order to determine the significance of this source of error. Results show that subsoil diffusion of 15N-labelled N2 and N2O – and thus potential underestimation of denitrification derived from chamber fluxes – increases with chamber deployment time as well as with increasing soil gas diffusivity. Simulations based on the range of typical soil gas diffusivities of unsaturated soils showed that the fraction of N2 and N2O evolved from 15N-labelled NO3- that is not emitted at the soil surface during 1 h chamber closing is always significant, with values up to >50 % of total production. This is due to accumulation in the pore space of the 15N-labelled soil and diffusive flux to the unlabelled subsoil. Empirical coefficients to calculate denitrification from surface fluxes were derived by modelling multiple scenarios with varying soil water content. Modelling several theoretical experimental set-ups showed that the fraction of produced gases that are retained in soil can be lowered by lowering the depth of 15N labelling and/or increasing the length of the confining cylinder. Field experiments with arable silt loam soil for measuring denitrification with the 15N gas flux method were conducted to obtain direct evidence for the incomplete surface emission of gaseous denitrification products. We compared surface fluxes of 15N2 and 15N2O from 15N-labelled micro-plots confined by cylinders using the closed-chamber method with cylinders open or closed at the bottom, finding 37 % higher surface fluxes with the bottom closed. Modelling fluxes of this experiment confirmed this effect, however with a higher increase in surface flux of 89 %. From our model and experimental results we conclude that field surface fluxes of 15N-labelled N2 and N2O severely underestimate denitrification rates if calculated from chamber accumulation only. The extent of this underestimation increases with closure time. Underestimation also occurs during laboratory incubations in closed systems due to pore space accumulation of 15N-labelled N2 and N2O. Due to this bias in past denitrification measurements, denitrification in soils might be more relevant than assumed to date. Corrected denitrification rates can be obtained by estimating subsurface flux and storage with our model. The observed deviation between experimental and modelled subsurface flux revealed the need for refined model evaluation, which must include assessment of the spatial variability in diffusivity and production and the spatial dimension of the chamber.


Sign in / Sign up

Export Citation Format

Share Document