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Published online 12 March 2007
Published in Soil Sci Soc Am J 71:336-346 (2007)
DOI: 10.2136/sssaj2006.0203
© 2007 Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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SOIL BIOLOGY & BIOCHEMISTRY

Modeling Soil Carbon and Nitrogen Dynamics in No-till and Conventional Tillage Using PASTIS Model

Katrien Oortsa, P. Garnierb, A. Findelingc, B. Maryd, G. Richarde and B. Nicolardotf,*

a INRA, Unité d'agronomie de Laon-Reims-Mons, 2 Esplanade Roland Garros, BP 224, 51686 Reims Cedex 2, France
b INRA, Unité d'Agronomie de Laon-Reims-Mons, rue Fernand Christ, 02007 Laon Cedex, France
c IRAD, Unité de Recherche Risque Environnemental, avenue Agropolis, 34398 Montpellier Cedex 5, France
d INRA, Unité d'Agronomie de Laon-Reims-Mons, rue Fernand Christ, 02007 Laon Cedex, France
e INRA, Unité de Science du Sol d'Orléans, 2163 Domaine de Limère, BP 20619, 45166 Olivet, France
f INRA, Unité d'agronomie de Laon-Reims-Mons, 2 Esplanade Roland Garros, BP 224, 51686 Reims Cedex 2, France

* Corresponding author (bernard.nicolardot{at}reims.inra.fr).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 CONCLUSIONS
 REFERENCES
 
The performance of the PASTIS model was evaluated to simulate soil C and N fluxes under real field conditions with conventional moldboard plowing (CT) and no-tillage (NT) systems differentiated for 33 yr for a loamy soil in northern France. Afterward, the influences on the C and N fluxes by soil temperature, soil water content, and quantity and localization of soil organic matter (SOM) and crop residues in the soil profile were determined. The model PASTIS was able to provide good simulations for the dynamics of soil water content and temperature, CO2 emissions, residue decomposition, and N mineralization. Simulation showed that the presence of the mulch layer in NT reduced cumulative total water evaporation and increased water drainage at the bottom of the 25-cm depth. Furthermore, simulation showed that the larger cumulative total CO2 flux in NT resulted from larger CO2 emissions as a product of crop residue decomposition and not as product of SOM decomposition. The larger amount of accumulated residues of previous crops in NT more than compensated for the slower residue decomposition rate of surface compared with incorporated residues. It was the water content of the surface crop residues that largely controlled the magnitude of this difference in decomposition rate of the crop residues between CT and NT. This means that, besides the amount of crop residues in both tillage systems, the distribution of rainfall and potential evaporation have a large influence on the differences in C and N fluxes between the two tillage systems

Abbreviations: CT, conventional moldboard plowing • NT, no-tillage • SOM, soil organic matter • TDR, time domain reflectometry


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 CONCLUSIONS
 REFERENCES
 
Compared with moldboard plowing (CT) systems, the introduction of NT systems modifies the location of crop residues and the distribution of SOM in the soil profile. In NT systems, crop residues are located in a mulch layer on top of the soil surface, while in CT systems, these residues are incorporated into the soil. In addition, the NT system induces changes in physical soil properties such as bulk density, the gas diffusion coefficient, and hydraulic conductivity. All these modifications, in turn, interact together on the water, temperature, and C and N dynamics in the soil.

Understanding and quantifying these complex interactions remains a challenging issue. Modeling allows extraction of the effect of each individual change. Many models exist where the decomposition of SOM and incorporated residues are coupled with water and heat fluxes, but only a few models simulate the impact of a mulch layer of crop residues. A mulch module exists in the Expert-N model (Berkenkamp et al., 2002), the APSIM model (Thorburn et al., 2001) and in the PASTIS model (Findeling et al., 2006). The decomposition of surface and incorporated residues in the Expert-N model is mainly differentiated by N limitation and the degree of contact with the soil. Coppens et al. (2006), however, found that the difference in decomposition between surface and incorporated residues is largely determined by the water content of these residues. The mulch modules in APSIM (Probert et al., 1998; Thorburn et al., 2001) and PASTIS (Findeling et al., 2006) take into account the effect of a surface mulch on the water dynamics of the whole mulch–soil system. Furthermore, the water and temperature dynamics and C and N transformations interact with each other in those models. Probert et al. (1998) simulated water and N dynamics in conventional and no-tillage systems with the APSIM model, but they evaluated the model only with long-term differences in water and NO3 content between the two systems. Coppens et al. (2004) used the PASTIS model to study the short-term effects of crop residue location on the water and C and N dynamics in soil under controlled laboratory conditions. Garnier et al. (2003) evaluated the PASTIS model for field conditions with incorporated straw in a CT system. The PASTIS model has not yet been evaluated for field conditions in NT systems, however.

The aim of our study was twofold: (i) to model the C and N fluxes under real field conditions with CT and NT differentiated for 33 yr, and (ii) to determine, by means of simulations, the influence of the main factors explaining the differences in CO2 emissions between the two tillage systems. These factors include soil temperature, soil water content, and the amount and localization of humified and fresh organic matter (crop residues). The influence of the location of crop residues as the effect of long-term changes in both biological and physical properties was taken into account.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 CONCLUSIONS
 REFERENCES
 
Experimental Setup
The study site is located at Boigneville in northern France (48°33' N, 2°33' E). Two tillage systems, NT and CT, have been differentiated since 1970. Before that, the two systems were yearly moldboard plowed to 30-cm depth. In this experiment, we studied two plots: the CT plot (Plot 224), which was yearly moldboard plowed to 20-cm depth, and the NT plot (Plot 223), which was only minimally disturbed along the sowing line by the sowing machine (<5 cm). Both have been cropped with a maize (Zea mays L.)–wheat (Triticum aestivum L.) rotation and crop residues have been returned to the soil every year. In the CT plot, crop residues remained on the soil surface until incorporation by tillage, while in the NT plot, crop residues always remained on the soil surface. The modeling period started on 19 Nov. 2003 (corresponding to plowing for CT) and ended at maize sowing on 13 Apr. 2004. During the entire period, the soil remained uncropped. The wheat crop had been harvested at the end of July 2003.

The soil is a Haplic Luvisol. The characteristics of the upper 0- to 25-cm soil layer of the two plots are presented in Table 1. Carbon dioxide was measured using automatic chambers (0.49 m2, 0.225 m high) connected to an infrared analyzer (Oorts, 2006). Four chambers for each tillage treatment were pressed 0.10 m into the soil. These gas chambers were placed on one line perpendicular to the direction of the field operations and covered the whole width of the combine harvester (4.5 m) to take into account the horizontal heterogeneity of both soil structure and the distribution of crop residues induced by tillage and harvest operations. The chambers closed four times a day for 5 min at 0400, 1000, 1600, and 2200 h. Carbon dioxide emissions were measured during these closure periods and the daily CO2 emissions were calculated each day as the average of these four measurements. Outside these closure periods, the chambers were left open to expose the soil inside the chambers to realistic weather conditions. Volumetric soil water content was measured using time domain reflectory (TDR) probes (Model CS616, Campbell Scientific, Shepshed, UK) connected to a data logger (Model CR10X, Campbell Scientific) and installed at 2.5-, 12.5-, and 25-cm soil depths. For each soil layer, these probes were calibrated with manual measurements of gravimetric water content and bulk density in the 0- to 5-, 5- to 20-, and 20- to 25-cm soil layers. Rainfall, potential evaporation, and air temperature were recorded by an automatic weather station at the experiment site. Soil temperature was recorded hourly with thermocouples at 0-, 2.5-, 12.5-, and 25-cm soil depths.


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Table 1. Soil properties of the conventional tillage (CT) and no-tillage (NT) field plots studied at Boigneville.

 
The amounts of surface and incorporated crop residues were quantified on 18 Nov. 2003 (the day before the tillage event) and 13 Apr. 2004 (the end of the simulation period). The C and N concentrations of the residues were determined using an elemental analyzer (NA 1500, Carlo Erba, Milan, Italy). Surface residues in NT were a combination of recently harvested wheat residues and older weathered maize and wheat residues. Maize and wheat plants have different natural 13C abundance. Thus, 13C measurements were performed using the elemental analyzer coupled to a mass spectrometer (Fisons Isochrom, Fisons, Manchester, UK) to estimate the part of the residue C derived from maize residues. At the end of the experiment, soil samples were taken from the 0- to 5-, 5- to 20-, and 20- to 25-cm layers inside the gas chambers. Total C and N of these samples were measured with the elemental analyzer and total microbial biomass C was determined by the fumigation extraction technique as described by Trinsoutrot et al. (2000a). Mineral N of the 0- to 5- and 0- to 25-cm soil layers was measured monthly as explained in Oorts et al. (2006a).

Model Description
The transfer of water, heat, and solute and the transformations of C and N in the soil of the CT and NT plots were modeled with the one-dimensional mechanistic model PASTIS (Prediction of Agricultural Solute Transformations In Soils; Lafolie, 1991), which includes two submodels: (i) a submodel that simulates the transport of water, solutes, and heat using classical equations, i.e., Richard's equation for water flow, the convection–dispersion equation for solute transport, and the convection–diffusion equation for heat flow (this submodel does not consider vapor phase transport, hysteresis of hydraulic properties, or preferential flow); and (ii) a submodel CANTIS (Carbon and Nitrogen Transformations In Soil; Garnier et al., 2001) which simulates the decomposition of organic matter, mineralization, immobilization, nitrification, and humification. Soil organic matter is divided into three nonliving organic pools: fresh, soluble, and humified organic matter and two living pools. The microbial population is split into an autochthonous biomass that decomposes humified organic matter and a zymogenous biomass that decomposes fresh and soluble organic matter. Crop residues are added to the fresh and soluble organic matter pool. The fresh organic matter pool consists of rapidly decomposable material, hemicellulose, cellulose, and lignin. Decomposition of fresh, soluble, and humified organic matter is assumed to follow first-order kinetics.

Garnier et al. (2003) evaluated the PASTIS model on field data collected during a 1-yr period from a CT system with incorporated wheat straw. Findeling et al. (2006) added a mulch module to the PASTIS model to simulate the water and C and N dynamics in the presence of a mulch of surface residues. This module takes into account the rain interception by the surface mulch and simulates changes in evaporation, thermal exchanges, and C and N transformations. The extended PASTIS model was tested with data obtained under controlled laboratory conditions.

Description of the Soil Profiles
The zero depth of the soil profiles was set at the soil–mulch interface. The NT plot was modeled down to 25 cm, which was below the plowing depth in CT. To take into account soil profiles with similar masses of dry soil in the two tillage systems, the CT soil profile was extended by 1 cm (0–26 cm). Below, the soil profiles in CT and NT are considered to be 0- to 25-cm soil profiles to simplify the discussion. The modeling was limited to a 0- to 25-cm soil profile for two reasons: (i) no crop residues were found below that depth, and (ii) total organic C and N concentrations were much lower below than above 25 cm.

The simulated NT soil profile consisted of two soil layers. The 0- to 5-cm soil layer had a loose structure, low bulk density, and high C and N concentrations. The 5- to 25-cm soil layer had a high bulk density, massive structure, and low C and N concentrations (Table 1). Crop residues in the NT plot were situated as a mulch (~2 cm thick) on the soil surface.

The simulated CT profile was divided into a 0- to 20-cm recent plow layer and a denser 20- to 25-cm soil layer. The actual 0- to 20-cm plow layer had a very heterogeneous structure with dense and compacted clods, loose soil, voids, and lumps of incorporated straw residues. Since PASTIS is a one-dimensional model, the heterogeneity in the plow layer had to be simplified. First, an average bulk density was taken for the whole recent plow layer (0–20 cm). Second, two vertical soil strips were defined based on field estimations of the proportion of the volume occupied by groups of crop residues across the whole soil area (Oorts, 2006): a soil strip containing all the incorporated crop residues (10% of the soil volume) and a soil strip without residues (90% of the soil surface volume). In the strip with crop residues, residues were homogeneously spread throughout the 5- to 20-cm layer because only a negligible amount of crop residues was observed in the 0- to 5-cm soil layer, as also observed in a study by Staricka et al. (1991). The two CT soil strips were simulated separately and then summed, taking their relative proportion of the soil volume into account.

Rainfall intensity and potential evapotranspiration were the surface boundary conditions for simulating water transport. At the bottom of the soil profile, a water pressure head was imposed. It was calculated using the measured volumetric water content and the water retention curve. The temperatures measured at depths of 0 and 25 cm were set as boundary conditions at the top and bottom, respectively.

Transport Parameters
The water flow parameters used in PASTIS are shown in Table 2. The water retention curve for each soil layer was determined in each tillage plot by measuring the soil water content of undisturbed soil samples under a succession of imposed water pressure heads: –0.1, –1, –10, –50, –100, and –1585 kPa. The suction table and low- and high-pressure chamber methods were used for the pressure ranges 0 to 10, 10 to 300, and 300 to 1600 kPa, respectively (Kabat and Beekma, 1994). The equation of van Genuchten (1980) was fitted to the experimental data:

Formula
where Se(h) is the effective saturation, {theta}r and {theta}s are the residual and saturated volumetric water contents, respectively (m3 m–3), {alpha} is the scaling factor of water pressure head (kPa–1), h is the water pressure head (kPa), and n is a dimensionless empirical shape parameter.


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Table 2. Water flow parameters used in the PASTIS model for the water retention and hydraulic conductivity curves of the different soil layers in the conventional tillage (CT) and no-tillage (NT) plots.

 
Hydraulic conductivity data were obtained using the WIND method (Tamari et al., 1993). The equation of van Genuchten (1980) was selected for the hydraulic conductivity curve:

Formula
where Ks is the saturated soil hydraulic conductivity (m s–1), m is a dimensionless empirical shape parameter, and l is the tortuosity parameter set to 0.5. The parameters Ks and m were optimized with the measured soil water content and the hydraulic conductivity data obtained by the WIND method.

Heat flow and solute parameters were taken from Garnier et al. (2001), who worked on a very similar loamy soil in Mons-en-Chaussée in northern France. They estimated the soil thermal conductivity coefficients by fitting the model to field data of temperatures at different depths. Their soil dispersivity of 1 cm, obtained by fitting the model to data from field leaching experiments with Cl, was used in our work.

Biological Parameters
The biological parameters of CANTIS were obtained from incubation experiments or taken from Garnier et al. (2003). Incubations of soil without added fresh organic matter were performed on 12.5-mm sieved fresh soil samples taken in the field gas chambers in the 0- to 5-, 5- to 20-, and 20- to 25-cm soil layers at the end of the measurement period. During these incubations, potential C and N mineralization of the soil samples was measured under controlled conditions (15°C and water pressure head of –63 kPa) for 168 d using the method described by Oorts et al. (2006b). The parameters used to describe the decomposition of humified organic matter, i.e., the decomposition rate of the autochthonous biomass kA, the decomposition rate of the humified organic matter kH, and the humification coefficient hA, were estimated by fitting the CANTIS submodel to the C and N mineralization data. It is not possible to enter different biological parameters for different soil layers in the PASTIS model. For the NT treatment, however, the soil from the 0- to 5-cm layer had a higher mineralization rate than the soil from the 5- to 20- and 20- to 25-cm soil layers. In addition, the 0- to 20-cm soil layer of the CT treatment also had a higher mineralization rate than the 20- to 25-cm layer. To minimize this problem, the kA, kH, and hA parameters were optimized with the mineralization data of the upper soil layer (Table 3). We then reduced the initial amounts of humified organic matter in the 5- to 20- and 20- to 25-cm layers of NT and the 20- to 25-cm layer of CT so that the calculated mineralization kinetics using the fixed biological parameters were similar to the measured mineralization kinetics.


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Table 3. Optimized biological parameters of the CANTIS submodel with the measured potential C and N mineralization in the conventional tillage (CT) and no-tillage (NT) plots.

 
The biomass-dependent factors for the decomposition of the humified and soluble organic matter, KMA and KMZ, respectively, were set to zero (i.e., no dependence of the decomposition rates on the size of the microbial biomass). The biological parameters used to describe the decomposition of fresh organic matter were taken from Garnier et al. (2003) because the same crop residue (wheat straw) was used.

Parameters of Mulch Module
The parameters specific for the mulch module were either measured, taken from the literature, or calibrated (Table 4). The covering proportion of the mulch was set to 1, based on field observations. The maximal and minimal volumetric water content of the mulch elements and the mulch density were taken from Garnier et al. (2004), who measured the hydraulic properties of wheat straw at Boigneville. The following parameters were calibrated: the mulch propensity to reduce soil evaporation ({xi}), the mulch propensity to water recharge ({alpha}m), the maximum depth for available N for mulch decomposition (zm,zyb), and the proportion of the mulch dry mass in contact with the soil. The calibration of these parameters was necessary for three reasons: (i) no references were found in the literature for them, (ii) they were not easily measurable, or (iii) they changed with the mulch type. The parameters {xi} and {alpha}m were calibrated with the soil water content of the 0- to 5-cm soil layer. The mulch propensity to water recharge ({xi}) determines the amount of water that is intercepted by the mulch and consequently the amount of water that is directly transferred to the soil. The parameter zm,zyb was calibrated within a 0- to 5-cm range by fitting the simulated to the observed NO3 content of the 0- to 5-cm soil layer. A value of 1 cm gave the best results. The initial proportion of the mulch dry mass in contact with the soil was calibrated by fitting the simulated to the measured CO2 emissions and resulted in a value of 100% contact of the mulch with the soil. This value is in accordance with the field observations of a thin mulch layer of surface residues with no standing stubble at the beginning of the simulation period. Those residues had remained at least 3.5 mo on the soil surface, which had reinforced the contact with the soil.


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Table 4. Parameters for the mulch module for the no-tillage plot.

 
Initial Conditions of Organic Matter Pools
The biochemical composition of the crop residues was determined using a modification of the method proposed by Van Soest and described in Trinsoutrot et al. (2000b). The neutral detergent fraction, hemicellulose, cellulose, and lignin fractions were separated. The soluble fraction of the residues was extracted by shaking in cold water at 20°C for 30 min. The C and N concentrations of the different fractions were determined by dry combustion using an NA 1500 elemental analyzer (Fisons, Milan, Italy). The rapidly decomposable material in PASTIS is defined as the difference between the neutral detergent fraction and the soluble fraction. The amount of fresh organic matter is equal to the sum of the rapidly decomposable material, hemicellulose, cellulose, and lignin fractions. The initial amount of zymogenous biomass C was estimated to be 25% of the measured total microbial biomass C. The initial conditions for the entire soil profile are listed in Table 5 and initial conditions for the different soil layers are shown in Table 6.


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Table 5. Initial conditions of the CANTIS submodel for the conventional tillage (CT) and no-tillage (NT) plots.

 

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Table 6. Initial sizes of the organic matter pools of the CANTIS submodel for the different soil layers in the conventional tillage (CT) and no-tillage (NT) plots.

 
Model Evaluation
The model was evaluated statistically for soil volumetric water content and temperature dynamics, CO2 emissions, and soil NO3 content. The efficiency (EF) and the mean difference (MD) were used to assess the model performance (Smith et al., 1996):

Formula

Formula
where mi and si are the measured and simulated results, and m is the average of the n measured results.


    RESULTS AND DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 CONCLUSIONS
 REFERENCES
 
Soil Temperature and Water Content
The temperature dynamics at 2.5- and 12.5-cm soil depth (not represented) were very well simulated with a model efficiency >0.97 (Table 7), with hourly temperatures at the 2.5-cm soil depth fluctuating between –4 and 19°C. Regarding the soil water dynamics, two periods could be distinguished (Fig. 1 ): an infiltration period from 19 Nov. 2003 until 28 Jan. 2004 and an evaporation period from 29 Jan. 2004 until 13 Apr. 2004.


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Table 7. Model efficiency (EF) and mean difference (MD) for the 0–5 and 5–20 cm soil layers of the conventional tillage (CT) and no-tillage (NT) plots.

 

Figure 1
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Fig. 1. Measured and simulated water contents of the 0- to 5- and 5- to 20-cm soil layers of the conventional tillage and no-tillage plots. Symbols are measured data, lines are simulated data.

 
The volumetric water content of the NT plot was well simulated by the model. The volumetric water content of the CT plot was badly simulated, however, especially for the 0- to 5-cm soil layer. This was probably due to the fact that the soil water content was measured during the period directly after tillage in the CT plot, a process that resulted in an highly heterogeneous structure with a lot of voids between loose and dense soil clods. Furthermore, the bulk density of the CT plot changed considerably during the simulation period. Coutadeur et al. (2002) found that, in a plowed field, the water flux progressed rapidly in zones with loose structure, whereas the water flux avoided dense structures. This means that when a TDR probe is located in a void or a loose structure, the water content measured by the TDR probe can rise and decrease suddenly. On the other hand, a TDR probe located in the middle of a big clod will not measure much variation in water content because most of the infiltrating water does not reach the middle of the clod. The spatial and temporal variability in the CT plot induced a bad calibration of the TDR with the manually measured water content (results not shown). This can explain, in combination with the absence of preferential flow in the PASTIS model, the bad agreement between simulations and measurements of the soil water content in CT.

The mean differences between measured and simulated values were acceptable for all soil layers except the 0- to 5-cm soil layer of CT (Table 7). Model efficiencies were rather low, but this was mainly due to the small variations in measured water contents. The large overestimation of the water content in the 0- to 5-cm soil layer in CT implied that the calculated values for the reduction function of moisture on SOM and crop residue decomposition were not reliable for this soil layer; however, only a small proportion of the total decomposition in CT occurred in the 0- to 5-cm layer since crop residues were mainly located in the 5- to 20-cm soil layer.

The differences in soil water content between CT and NT (Fig. 1) were not only due to the presence of the mulch layer (e.g., the effect on water evaporation as mentioned below), but also resulted from differences in the water retention curves after 33 yr of tillage differentiation (Table 2). The 0- to 5-cm layer of NT presented both larger volumetric water contents at low water pressure heads and smaller volumetric water contents at high water pressure heads than the other soil layers of NT and CT. This difference in the water retention curve could be due to the larger organic matter content (Gupta et al., 1977) and the lower bulk density (Reicosky et al., 1981) in the 0- to 5-cm layer of NT. As a consequence, the 0- to 5-cm soil layer of NT had larger gravimetric and volumetric soil water contents than the other soil layers, although simulated water pressure heads were similar in all soil layers of the CT and NT profile. No large differences were found between the water retention curves of the CT treatment and the 5- to 25-cm soil layer of the NT treatment, which is in accordance with the literature on this subject (Wu et al., 1992; Benjamin, 1993; Hubbard et al., 1994; Lal, 1999; Blanco-Canqui et al., 2004; Fuentes et al., 2004). The unsaturated hydraulic conductivity as a function of the water pressure head in the equivalent plow layer follows the order NT (0–5 cm) > CT (0–20 cm) > NT (5–20 cm). There is no consensus in the literature on the effect of tillage on the unsaturated hydraulic conductivity as a function of the water pressure head: some researchers have reported larger values for NT (Dao, 1993; Fuentes et al., 2004), while others have reported similar values for CT and NT (Datiri and Lowery, 1991; Wu et al., 1992; Benjamin, 1993).

Water Content of Mulch
The simulated volumetric water content of the mulch remained close to saturation during the infiltration period because evaporation was not large enough to evaporate mulch water between two rainfalls. In contrast, large fluctuations were simulated during the evaporation period (Fig. 2 ).


Figure 2
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Fig. 2. Simulated water contents of the surface mulch of the no-tillage plot.

 
Total Evaporation and Water Drainage
Total evaporation is defined as the sum of the evaporation from the soil and the mulch. During the infiltration period, the cumulative total evaporation and water drainage at 25-cm depth simulated by the model were comparable between the two tillage systems (Fig. 3 ). During the evaporation period, cumulative total evaporation was lower, whereas cumulative water drainage was larger in NT than CT. During the entire simulation period, NT presented a 38% smaller cumulative total evaporation and a 33% larger cumulative water drainage. Total evaporation was lower due to a reduction of soil evaporation by the mulch layer. The difference in total evaporation between the two tillage systems (38 mm) was considerably larger than the maximum water storage of the mulch (4 mm). This means that more water entered the soil in NT than in CT, which generated the greater water drainage at 25-cm depth in NT. The value of 0.6 for the reduction of soil evaporation by the mulch is greater than the value found by Findeling (2002), but this is consistent with a denser mulch in our experiment. The 100% surface cover of crop residues estimated from photographs (Oorts, 2006) was in accordance with the surface cover observed by Steiner et al. (2000) for similar masses of flat wheat residues.


Figure 3
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Fig. 3. Simulated cumulative total evaporation at the top and water drainage at the bottom of the 0- to 25-cm soil profile of the conventional tillage (CT) and no-tillage (NT) plots.

 
Crop Residues Decomposition
Due to the presence of old weathered residues from previous years (Oorts, 2006), the initial amount of C in crop residues was much larger in NT (3430 kg C ha–1) than CT (1464 kg C ha–1) (Fig. 4 ). In CT, only crop residues of the recent wheat harvest were present. Simulated and measured C decomposition corresponded well in both CT and NT treatments. During the infiltration period, the simulated C decay in NT (809 kg C ha–1) was 70% higher than in CT (471 kg C ha–1), whereas during the evaporation period, C decay was 30% higher for NT (429 kg C ha–1) than CT (319 kg C ha–1). In both periods, however, the relative decay rate was smaller in NT than in CT: 24% compared with 32%, respectively, during the infiltration period and 13% compared with 22%, respectively, during the evaporation period. The slower decomposition was consistent with the accumulation of weathered surface residues in NT. This means that the greater amount of crop residues in NT offset the slower residue decomposition. The slower C decay in NT may partly result from the presence of old residues that decompose more slowly than recently added residues or from a (slightly) larger limitation of decomposition by a mineral N deficiency due to reduced soil contact in NT compared with CT. The difference in soil contact between the two tillage systems was reduced, however, because residues were incorporated in clusters in CT instead of being homogenously distributed throughout the plow layer (Henriksen and Breland, 2002). The effect of soil climate on the decomposition rate of crop residues is discussed below.


Figure 4
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Fig. 4. Measured and simulated amounts of C in crop residues of the conventional tillage (CT) and no-tillage (NT) plots. Bars indicate standard errors of the measured values.

 
Soil Inorganic Nitrogen
The mineral N content in the soil profile is the result of (i) the N mineralization and immobilization processes during the decomposition of SOM and crop residues and (ii) the transport processes of inorganic N (N leaching and convective transport by capillary rise).

The evolution of the NO3–N content in the 0- to 5- and 0- to 25-cm soil layers was first simulated using a standard procedure with a one-dimensional simulation model, i.e., assuming that the crop residues were homogeneously distributed across the horizontal plane. This procedure provided a good simulation for NT, but not for the CT plot (Fig. 5 ). The model underestimated the amounts of soil mineral N in the CT plot, particularly in the 5- to 25-cm layer. The model was thought to overestimate the amount of immobilized N, probably because it overestimated the availability of mineral N. Indeed, the one-dimensional model assumes that all mineral N present at a given depth is available for residue decomposition at this depth. This hypothesis is likely to be false, mainly because crop residues incorporated by moldboard plowing are not evenly distributed throughout the soil volume, but situated in residue clusters in zones with high porosity between two adjacent furrows, as also observed by Staricka et al. (1991). Gaillard et al. (1999) determined that straw incorporation increases the microbial activity only in a zone of 0.4 cm around the crop residues. This suggests that only the soil mineral N near the residues was available for the microbial biomass that decomposed the residues. The mineral N situated farther from the residues was not available for residue decomposition. The impact of this heterogeneity in residue location was tested with our one-dimensional model by assuming that the modeled soil volume in CT was composed of two vertical soil strips: a first strip free of crop residues (90% of the soil volume) and a second strip containing all the crop residues (10% of the soil volume). These figures were consistent with the observations made in the field. The simulations were run separately for each strip and the outputs were summed according to the respective soil volume of each strip. The model thus parameterized was able to reproduce the observed soil NO3–N content well (Fig. 6 ). The mineral N had disappeared completely in the strip with residues due to N immobilization, whereas mineral N accumulated in the strip without residues due to net mineralization. The residue decomposition rate was markedly reduced due to this N limitation. The model assumed no mineral N exchange between the two strips so that the NO3–N present in the strip without residues was not available for residue decomposition in the strip with residues.


Figure 5
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Fig. 5. Measured and simulated NO3–N contents in the 0- to 5- and 0- to 25-cm soil layers in the conventional tillage plots under the assumption that crop residues in the PASTIS model are homogeneously distributed throughout the entire soil volume. Bars indicate standard errors of the measured values.

 

Figure 6
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Fig. 6. Measured and simulated NO3–N contents in the 0- to 5- and 0- to 25-cm soil layers in the conventional tillage (CT) and no-tillage plots, under the assumption that crop residues in CT are located in 10% of the entire soil volume. Bars indicate standard errors of the measured values.

 
In NT, decomposition of the surface residues was also limited by the amount of mineral N, since only the first centimeter of soil could provide mineral N. Fungi form a bridge between the mulch layer and the soil and translocate mineral N from the surface soil to the mulch, while C is transferred from the mulch to the surface soil (Frey et al., 2003). The model responded to the mineral N limitation by the simulation of both a reduction in decomposition rate and an increase in the C/N ratio of the decomposing (zymogeneous) biomass. These changes resulted in a reduced decomposition of residues and lower CO2 emissions compared with nonlimiting conditions. The model predicted a cumulative gross N mineralization of 171 kg N ha–1 for CT and 164 kg N ha–1 for NT, a cumulative gross N immobilization of 147 kg N ha–1 for CT and 130 kg N ha–1 for NT, and a cumulative net mineralization of 24 kg N ha–1 for CT and 34 kg N ha–1 for NT.

The calculated amount of cumulative NO3–N leached below the 25-cm soil depth was 22 kg N ha–1 for CT and 45 kg N ha–1 for NT during the entire study period. The larger N leaching in NT was mainly the result of the larger initial NO3–N content and the larger amount of drainage. For both tillage systems, N leaching during the evaporation period was negligible. There is no consensus about the effect of tillage on N leaching in the literature (Elliott and Coleman, 1988; Germon et al., 1994; Shipitalo et al., 2000).

Carbon Dioxide Emissions
The simulations of CO2 production were also initiated with the standard procedure, assuming an even distribution of crop residues (one soil volume). They lead to the same conclusions as for mineral N: the simulations were quite satisfactory for NT, but they overestimated the cumulative CO2 production in the CT plot (not shown). The simulations conducted with two soil volumes (two vertical strips) again resulted in very good simulations in the CT plot (Fig. 7 ). It is noteworthy that the cumulative CO2 production was greater in NT than in CT plot.


Figure 7
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Fig. 7. Measured and simulated cumulative CO2 emission in the conventional tillage (CT) and no-tillage (NT) plots, under the assumption that crop residues in CT are located in 10% of the entire soil volume.

 
Considering the daily CO2 fluxes in the NT plot, both the magnitude and the fluctuations of the daily CO2 emissions were very well simulated (Fig. 8 ). In CT, however, the timing and the magnitude of the peaks or dips of the daily CO2 emissions were not always well reproduced. The measured CO2 emissions, normalized for a temperature of 15°C (Rodrigo et al., 1997), decreased in the CT plot during and shortly after rainfall events. This may be explained by reduced gas diffusivity in wet soils (Currie, 1984), i.e., CO2 gases were captured in the soil profile. This captured CO2 gas escaped from the soil profile between rainfall events. The discrepancies between the simulated and observed daily CO2 emissions in CT can be explained by the fact that the PASTIS model does not account for reduced gas diffusivity in wet soils. Although the model may simulate well CO2 production by the soil, it may overestimate CO2 fluxes soon after rainfall and underestimate CO2 fluxes later between rainfall events. This probably explains why the cumulative CO2 fluxes were well simulated in CT. In NT, the reduction in gas diffusivity had less impact because most of the CO2 was produced in the mulch layer and near the soil surface (0–5-cm soil layer).


Figure 8
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Fig. 8. Measured and simulated daily CO2 emissions in the conventional tillage (CT) and no-tillage plots, under the assumption that crop residues in CT are located in 10% of the entire soil volume. Bars indicate standard errors of the measured values.

 
The model was used to analyze the origins of the CO2 fluxes. It calculated that about half of the CO2 was produced during the decomposition of stabilized SOM and the other half during the decomposition of crop residues (Fig. 8). The CT and NT treatments presented the same CO2 emissions as a product of SOM decomposition (Fig. 9 ), even if we consider the daily CO2 emissions (Fig. 10 ). The potentials of CO2 emission from SOM measured under controlled laboratory conditions for the 0- to 25-cm soil profile were also similar between CT (1042 ± 47 kg CO2–C ha–1) and NT (980 ± 71 kg CO2–C ha–1) (Oorts 2006). This suggests that during the simulation period, soil climatic conditions had a similar effect on SOM decomposition in CT and NT. Indeed, the influence of soil temperature on the differences between CT and NT was negligible during the simulated period. Furthermore, most of the time, the reduction function on SOM decomposition due to water content calculated by the model varied between 0.9 and 1, indicating that water conditions were close to optimum for decomposition in both systems. In other periods of the year, however, differences in water content and soil temperature between CT and NT may play a significant role in SOM decomposition (Oorts, 2006). Despite similar CO2 emissions from SOM for the entire 0- to 25-cm soil profile, differences between CT and NT were calculated in the location of the production of CO2. This CO2 production was more pronounced near the soil surface in NT, whereas it was more homogeneously distributed throughout the whole 0- to 25-cm layer in CT (in accordance with the observed distribution of the SOM emissions potentials found in the laboratory incubations reported in Oorts et al. [2006b]).


Figure 9
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Fig. 9. Simulated cumulative CO2 emissions as a product of decomposition of soil organic matter (SOM) and crop residues in the conventional tillage (CT) and no-tillage (NT) plots, under the assumption that crop residues in CT are located in 10% of the entire soil volume.

 

Figure 10
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Fig. 10. Simulated daily CO2 emissions as a product of decomposition of soil organic matter (SOM) and crop residues in the conventional tillage (CT) and no-tillage (NT) plots, under the assumption that crop residues in CT are located in 10% of the entire soil volume.

 
The simulated cumulative CO2 fluxes produced during crop residue decomposition were 51% larger in NT than CT (Fig. 9). In spite of the slower residue decomposition in NT, the greater amount of crop residues (residues from previous years) resulted in a larger C decay. The CO2 produced during crop residue decomposition during the entire infiltration period accounts for 81% of the difference observed during the entire simulation period. During this infiltration period, the daily emissions followed the same dynamics in CT and NT, but their magnitude was larger in NT (Fig. 10). During the evaporation period, the simulated peaks of daily CO2 emissions did not occur at the same moment in time in CT and NT. During this period, daily emissions from residues in NT followed the same dynamics as the water content of the mulch layer (Fig. 2). Soil temperature had a similar effect on the surface and incorporated residues during the simulation period. The water content of the crop residues, however, largely controlled the magnitude of the difference in CO2 emissions between CT and NT. When the water content of the mulch remained optimal for decomposition (i.e., during the infiltration period), CO2 emissions in the NT system were much larger than in CT. During the evaporation period, however, the low water content of the mulch limited the residue decomposition in NT, thereby decreasing the difference in CO2 emissions between CT and NT. This resulted in bursts of CO2 emissions in the NT plot, whereas emissions were more constant in CT. Note that, despite the larger C amounts in NT, severe limitation of the mulch decomposition by water sometimes resulted in larger CO2 emissions in CT (where abiotic factors remained favorable) than in NT, e.g., in dry periods with high evaporation. The effect of the water content of the residues is confirmed in the literature. Abiven et al. (2002) measured no difference in cumulative CO2 emissions between surface and incorporated wheat straw under optimal moisture, temperature, and N conditions in the laboratory. Under variable moisture conditions, Coppens et al. (2006) observed lower cumulative CO2 emissions for surface than incorporated residues in the laboratory, mainly due to a difference in water content of the residues.


    CONCLUSIONS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 CONCLUSIONS
 REFERENCES
 
The model was able to provide good simulations of the evolution of soil water content, soil temperature, CO2 emissions, crop residue decomposition, and soil mineral N during a 5-mo period in the two tillage systems. The measurement and simulation of the soil water content of CT turned out to be difficult, due to the large spatial and temporal variations of both soil structures and properties directly after moldboard plowing. The simulation of the NT treatment was easier to carry out because of the more homogeneous soil structure.

The mulch layer exerted a large influence on the water dynamics: evaporation was reduced while water drainage increased. Cumulative and daily CO2 emissions produced during SOM decomposition were similar in both tillage systems, which was a result of similar CO2 emission potentials and similar regimes of soil temperature and water pressure head. The observed difference in CO2 emissions between the two tillage systems (larger in NT) was due to crop residue decomposition. Despite a slower decomposition of crop residues in NT, the larger amount of crop residues gave rise to a larger amount of C decay in NT. The larger amount of crop residues in NT was due to the presence of weathered residues from previous crops resulting from the slower residue decomposition in NT. No large temperature differences were observed between the surface residues in NT and the incorporated residues in CT. The water content of the mulch had the largest influence on the difference in decomposition rate of crop residues between CT and NT. Between rainfall events in periods with larger amounts of evaporation, the rate of residue decomposition in NT was reduced compared with CT due to the low water content of the surface residues.

For long-time differentiated CT and NT fields, the simulation results showed that the large amount of accumulated organic matter on the soil surface in NT can counterbalance the slower decomposition rate and result in larger CO2 emissions in NT than CT under specific climatic conditions. Finally, as the climatic variables had a large influence on the simulated CO2 fluxes between CT and NT, it would be interesting to run the model with data from fields under other climatic conditions.


    ACKNOWLEDGMENTS
 
Katrien Oorts was supported by a grant from ADEME and ARVALIS-Institut du Végétal. We would like to thank G. Alavoine, E. Gréhan, C. Herre, M.J. Herre, F. Millon, S. Millon, P. Regnier, and P. Thiébeau for their valuable laboratory and field assistance and ARVALIS-Institut du Végétal, especially J. Labreuche and D. Couture, for the conductance of the long-term field experiment at Boigneville.

Received for publication May 31, 2006.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS AND DISCUSSION
 CONCLUSIONS
 REFERENCES
 





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