Nitrous oxide evolution from structurally intact soil as influenced by tillage and soil water content
Introduction
Within arable agriculture, tillage is employed to improve soil tilth, to control weeds, and to incorporate crop residues, manure and fertilizers. In some regions, like the North American Great Plains, shallow tillage (ST) and no-till practices have been widely adopted to conserve soil water and to control soil erosion (Carter, 1994). Arable soils in Europe are typically mouldboard ploughed (Riley et al., 1994; Rasmussen, 1999), but the lower costs for fuel, machinery and labour associated with reduced tillage have stimulated the interest in such practices among farmers.
Reduced tillage further has a potential for mitigating anthropogenic greenhouse gas emissions to the atmosphere via carbon sequestration (Smith et al., 1998b). However, the absence of tillage may lead to soil compaction, reduced air-filled porosity and reduced availability of oxygen (Douglas et al., 1980; Schjønning, 1989; Ball et al., 1997; Gregorich et al., 2006; Sasal et al., 2006). Moreover, decomposition of crop residues is concentrated near the soil surface where the potential for leakage of gaseous products to the atmosphere is high. It has lead to concerns that benefits from C sequestration may be partly offset by an increase in emissions of the potent greenhouse gas nitrous oxide (N2O). Nitrous oxide is a free intermediate of denitrification, as well as a by-product of ammonia oxidation and a product of nitrifier–denitrification (Oenema et al., 2005). The production of N2O is stimulated under low oxygen conditions; Bollmann and Conrad (1998) found that the release of N2O from both nitrification and denitrification peaked at partial pressures <0.5% O2. Unless nitrite accumulates, denitrification is probably the only significant source of N2O (Rudaz et al., 1991; Kester et al., 1997).
Many field studies have tried to link management effects on N2O emissions to individual soil properties, but relationships are usually weak and system-specific, and soil water content often interacts with the effect of other soil variables (Robertson, 1994; Velthof et al., 1996; Burton et al., 1997; Bollmann and Conrad, 1998; Schmidt et al., 2000; Simek et al., 2006). Therefore, causal relationships have also been studied in manipulation experiments where some of the variability can be eliminated or controlled. In this way, for example, the effects of nitrite and nitrate availability (Firestone et al., 1979), air-filled porosity and nitrate (Letey et al., 1980), soil pH (Stevens et al., 1998) and C source (Gregorich et al., 2006) on N2O and N2 evolution have been investigated.
A significant proportion of annual N2O emissions occurs after rainfall events (Li et al., 1992). The sudden increase in soil water content typically causes a flush of C and (net) N mineralization increasing substrate availability for nitrification and denitrification. This may be due to microbial stress (Kieft et al., 1987; Fierer and Schimel, 2003), soil organic matter exposure by physical disruption of aggregates (Goebel et al., 2005), or alleviation of diffusional constraints (Schjønning et al., 2003). However, wetting also causes a change in gas diffusivity that will affect the exchange of oxygen and denitrification products between soil and the atmosphere. Irrespective of the mechanism, it is imperative that in studies on the regulation of N2O emissions the structural integrity of the soil–biota system is not disturbed prior to investigation.
We examined effects of tillage and soil water content on CO2 and N2O evolution in four distinct environments, i.e., two depth intervals of shallow-tilled and mouldboard-ploughed soil, by multiple linear regression analyses. Structurally intact soil cores were incubated at a range of matric potentials, the basic assumption being that effects of tillage system and soil water on microbial activities would reflect effects under field conditions. We hypothesized that effects and interactions of tillage and soil characteristics would lead to different patterns of N2O regulation among the four environments and two soil types used in our study.
Section snippets
Sites and management
Soil was sampled in tillage experiments at two field sites, Dronninglund (57°08N, 10°17E) and Nakskov (54°53N, 11°10E). According to the WRB(FAO) system, the Dronninglund soil is a Humic Dystric Cambisol, while the Nakskov soil is a Gleyic Luvisol (Krogh and Greve, 1999). The soil at Dronninglund is a fine sandy soil, while that at Nakskov is a sandy loam (Table 1). The Dronninglund experiment was initiated in 2000 and involves mouldboard ploughing (MP) to ca. 20 cm depth and non-inversive ST to
Soil characteristics
Selected characteristics of the plough layer at the Dronninglund and Nakskov sites were obtained at the block level; mean values and ranges are given in Table 1. The two soil types differed in several ways, with the Nakskov soil being texturally more graded and with a higher clay content, with lower soil C and N contents, and with a higher pH compared to the Dronninglund soil. The soils also differed with respect to organic inputs via fertilizers and crop residues, but the higher C content in
The experimental system
The observed distribution of PAO and DEA in the four distinct soil environments confirmed earlier studies showing that tillage practice influences the distribution of microbial populations (e.g., Doran, 1980; Linn and Doran, 1984). The consistent pattern with ST>MP at 0–4 cm depth and the opposite trend at 14–18 cm depth (Fig. 5) is in accordance with the observations of Staley et al. (1990), who examined potential nitrification and denitrification activity at 0–3.8 and 7.6–15 cm across a growth
Acknowledgements
The technical assistance of Anette Clausen, Mette Nielsen, Karin Dyrberg, Bodil Christensen and Stig Rasmussen is gratefully acknowledged. The authors are indepted to Kristian Kristiansen for advice on the statistical analyses.
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