Short- and long-term effects of nitrogen fertilization on methane oxidation in three Swedish forest soils

 Under normal conditions, CH₄, one of the most important greenhouse gases, is subject to biological oxidation in forest soils. However, this process can be negatively affected by N amendment. The reported experiment was conducted in order to study the short- and long-term effects of N amendment on CH₄ oxidation in pine (Pinus sylvestris L.) forest soils. Soil samples were taken from three experimental sites, two of which had been amended with N once, over 20 years earlier, while the third had been amended 3 weeks earlier. The soil samples were incubated fresh at 15  °C at ambient CH₄ concentrations (ca. 1.8 ppmv CH₄). The variation in CH₄-turnover rates was high within the treatments: CH₄ was produced [up to 22.6 pmol CH₄ g dry wt. soil^–1 h^–1] in samples from the recently amended site, whereas it was consumed at high rates (up to 431 pmol CH₄ g dry wt. soil^–1 h^–1) in samples from the plot that had received the highest N amendment 27 years before sampling. Although no significant differences were found between N treatments, in the oldest plots there was a correlation between consumption of atmospheric CH₄ and the total C content at a depth of 7.5–15 cm in the mineral soil (r ²=0.74). This indicates that in the long-term, increased C retention in forest soils following N amendment could lead to increased CH₄ oxidation. Received: 3 September 1997     

The influence of land use and pesticides on methane oxidation in some Belgian soils

 In a first experiment, the effect of land use on the uptake rate of atmospheric CH₄ was studied in laboratory incubations of intact soil cores. A soil under deciduous forest showed the highest CH₄ oxidation. Its overall CH₄ uptake during the measuring period (202 days) was 1.03 kg CH₄ ha^–1. Natural grassland showed the second highest CH₄ oxidizing capacity (0.71 kg CH₄ ha^–1). The overall amount of CH₄ uptake by fertilized pasture was 0.33 kg CH₄ ha^–1. CH₄ oxidation in arable soils with different fertilizer treatments varied between 0.34 and 0.37 kg CH₄ ha^–1. Undisturbed soils had a higher CH₄ uptake capacity than agricultural soils. The moisture content of the soil was found to be an important parameter explaining temporal variations of CH₄ oxidation. Different methods of fertilization which had been commenced 10 years previously were not yet reflected in the total CH₄ uptake rate of the arable soil. In a second experiment, a number of frequently used pesticides were screened for their possible effect on CH₄ oxidation. In a sandy arable soil lenacil, mikado and oxadixyl caused significantly reduced CH₄ oxidation compared to the control. Under the same conditions, but in a clayey arable soil, mikado, atrazine and dimethenamid caused a reduction of the CH₄ uptake. In a landfill cover soil, with a 100-fold higher CH₄ oxidation rate, no inhibition of CH₄ oxidation was observed, not even when the application rate of pesticides was tenfold higher than usual. Received: 1 December 1998     

Increased moisture and methanogenesis contribute to reduced methane oxidation in elevated CO2 soils

Awareness of global warming has stimulated research on environmental controls of soil methane (CH₄) consumption and the effects of increasing atmospheric carbon dioxide (CO₂) on the terrestrial CH₄ sink. In this study, factors impacting soil CH₄ consumption were investigated using laboratory incubations of soils collected at the Free Air Carbon Transfer and Storage I site in the Duke Forest, NC, where plots have been exposed to ambient (370 μL L⁻¹) or elevated (ambient + 200 μL L⁻¹) CO₂ since August 1996. Over 1 year, nearly 90% of the 360 incubations showed net CH₄ consumption, confirming that CH₄-oxidizing (methanotrophic) bacteria were active. Soil moisture was significantly (p < 0.01) higher in the 25–30 cm layer of elevated CO₂ soils over the length of the study, but soil moisture was equal between CO₂ treatments in shallower soils. The increased soil moisture corresponded to decreased net CH₄ oxidation, as elevated CO₂ soils also oxidized 70% less CH₄ at the 25–30 cm depth compared to ambient CO₂ soils, while CH₄ consumption was equal between treatments in shallower soils. Soil moisture content predicted (p < 0.05) CH₄ consumption in upper layers of ambient CO₂ soils, but this relationship was not significant in elevated CO₂ soils at any depth, suggesting that environmental factors in addition to moisture were influencing net CH₄ oxidation under elevated CO₂. More than 6% of the activity assays showed net CH₄ production, and of these, 80% contained soils from elevated CO₂ plots. In addition, more than 50% of the CH₄-producing flasks from elevated CO₂ sites contained deeper (25–30 cm) soils. These results indicate that subsurface (25 cm+) CH₄ production contributes to decreased net CH₄ consumption under elevated CO₂ in otherwise aerobic soils.     

Short-term effects of nitrogen on methane oxidation in soils

 The short-term effects of N addition on CH₄ oxidation were studied in two soils. Both sites are unfertilized, one has been under long-term arable rotation, the other is a grassland that has been cut for hay for the past 125 years. The sites showed clear differences in their capacity to oxidise CH₄, the arable soil oxidised CH₄ at a rate of 0.013 μg CH₄ kg^–1 h^–1 and the grassland soil approximately an order of magnitude quicker. In both sites the addition of (NH₄)₂SO₄ caused an immediate reduction in the rate of atmospheric CH₄ oxidation approximately in inverse proportion to the amount of NH₄ ⁺ added. The addition of KNO₃ caused no change in the rate of CH₄ oxidation in the arable soil, but in the grassland soil after 9 days the rate of CH₄ oxidation had decreased from 0.22 μg CH₄ kg^–1 h^–1 to 0.13 μg CH₄ kg^–1 h^–1 in soil treated with the equivalent of 192 kg N ha^–1. A ¹⁵N isotopic dilution technique was used to investigate the role of nitrifiers in regulating CH₄ oxidation. The arable soil showed a low rate of gross N mineralisation (0.67 mg N kg^–1 day^–1), but a relatively high proportion of the mineralised N was nitrified. The grassland soil had a high rate of gross N mineralisation (18.28 mg N kg^–1 day^–1), but negligible nitrification activity. It is hypothesised that since there was virtually no nitrification in the grassland soil then CH₄ oxidation at this site must be methanotroph mediated. Received: 31 October 1997     

Methane uptake in Swedish forest soil in relation to liming and extra N-deposition

Methane uptake to soil was examined in individual chambers at three small forest catchments with different treatments, Control, Limed and Nitrex sites, where N-deposition was experimentally increased. The catchments consisted of both well-drained forest and wet sphagnum areas, and showed uptake of CH₄ from the ambient air. The lowest CH₄ uptakes were observed in the wet areas, where the different treatments did not influence the uptake rate. In the well-drained areas the CH₄ uptakes were 1.6, 1.4 and 0.6 kg ha^–1 year^–1 for the Limed, Control and Nitrex sites, respectively. The uptake of methane at the well-drained Nitrex site was statistically smaller than at the other well-drained catchments. Both acidification and increase in nitrogen in the soil, caused by the air-borne deposition, are the probable cause for the reduction in the methane uptake potential. Uptake of methane was correlated to soil water content or temperature for individual chambers at the well-drained sites. The uptake rate of methane in soil cores was largest in the 0- to 10-cm upper soil layer. The concentration of CH₄ in the soil was lower than the atmospheric concentration up to 30 cm depth, where methane production occurred. Besides acting as a sink for atmospheric methane, the oxidizing process in soil prevents the release of produced methane from deeper soil layers reaching the atmosphere. Received: 27 September 1996     

Nitrous oxide emissions and methane oxidation by soil following cultivation of two different leguminous pastures

 Nitrous oxide (N₂O) emissions and methane (CH₄) consumption were quantified following cultivation of two contrasting 4-year-old pastures. A clover sward was ploughed (to 150–200 mm depth) while a mixed herb ley sward was either ploughed (to 150–200 mm depth) or rotovated (to 50 mm depth). Cumulative N₂O emissions were significantly greater following ploughing of the clover sward, with 4.01 kg N₂O-N ha^–1 being emitted in a 48-day period. Emissions following ploughing and rotovating of the ley sward were much less and were not statistically different from each other, with 0.26 and 0.17 kg N₂O-N ha^–1 being measured, respectively, over a 55-day period. The large difference in cumulative N₂O between the clover and ley sites is presumably due to the initially higher soil NO₃ ^– content, greater water filled pore space and lower soil pH at the clover site. Results from a denitrification enzyme assay conducted on soils from both sites showed a strong negative relationship (r=–0.82) between soil pH and the N₂O:(N₂O+N₂) ratio. It is suggested that further research is required to determine if control of soil pH may provide a relatively cheap mitigation option for N₂O emissions from these soils. There were no significant differences in CH₄ oxidation rates due to sward type or form of cultivation. Received: 1 November 1998     

Influence of N and non-N salts on atmospheric methane oxidation by upland boreal forest and tundra soils

 The short-term (24 h) and medium-term (30 day) influence of N salts (NH₄Cl, NaNO₃ and NaNO₂) and a non-N salt (NaCl) on first-order rate constants, k (h^–1) and thresholds (C_Th) for atmospheric CH₄ oxidation by homogenized composites of upland boreal forest and tundra soils was assessed at salt additions ranging to 20 μmol g^–1 dry weight (dw) soil. Additions of NH₄Cl, NaNO₃ and NaCl to 0.5 μmol g^–1 dw soil did not significantly decrease k relative to watered controls in the short term. Higher concentrations significantly reduced k, with the degree of inhibition increasing with increasing dose. Similar doses of NH₄Cl and NaCl gave comparable decreases in k relative to controls and both soils showed low native concentrations of NH₄ ⁺-N (≤1 μmol g^–1dw soil), suggesting that the reduction in k was due primarily to a salt influence rather than competitive inhibition of CH₄ oxidation by exogenous NH₄ ⁺-N or NH₄ ⁺-N released through cation exchange. The decrease in k was consistently less for NaNO₃ than for NH₄Cl and NaCl at similar doses, pointing to a strong inhibitory effect of the Cl^– counter-anion. Thresholds for CH₄ oxidation were less sensitive to salt addition than k for these three salts, as significant increases in C_Th relative to controls were only observed at concentrations ≥1.0 μmol g^–1 dw soil. Both soils were more sensitive to NaNO₂ than to other salts in the short term, showing a significant decrease in k at an addition of 0.25 μmol NaNO₂ g^–1 dw soil that was clearly attributable to NO₂ ^–. Soils showed no recovery from NaCl, NH₄ ⁺-N or NaNO₃ addition with respect to atmospheric CH₄ oxidation after 30 days. However, soils amended with NaNO₂ to 1.0 μmol NaNO₂ g^–1 dw showed values of k that were not significantly different from controls. Recovery of CH₄-oxidizing ability was due to complete oxidation of NO₂ ^–-N to NO₃ ^–-N. Analysis of soil concentrations of N salts necessary to inhibit atmospheric CH₄ oxidation and regional rates of N deposition suggest that N deposition will not decrease the future sink strength of upland high-latitude soils in the atmospheric CH₄ budget. Received: 30 April 1999     

Factors influencing nitrous oxide and methane emissions from minerotrophic fens in northeast Germany

 At two field sites representing northeastern German minerotrophic fens (Rhin-Havelluch, a shallow peat site; Gumnitz, a partially drained peat site) the influence of different factors (N fertilization, groundwater table, temperature) on N₂O and CH₄ emissions was investigated. The degraded fens were sources or sinks of the radiatively active trace gases investigated. The gas fluxes measured were much higher than those found in other terrestrical ecosystems such as forests. Lowering the groundwater table increased the release of N₂O and the oxidation of CH₄. High CH₄ emission rates occurred when the groundwater tables and soil temperatures were high (>12  °C). N fertilization stimulated the release of N₂O only when application rates were very high (480 kg N ha^–1). A moderate N supply (60 or 120 kg N ha^–1) hardly increased the release of N₂O in spite of high soluble soil NO₃ ^– contents. Received: 31 October 1997     

Potential contribution of Lumbricus terrestris L. to carbon dioxide, methane and nitrous oxide fluxes from a forest soil

 Potential effects of earthworms (Lumbricus terrestris L.) inoculated into soil on fluxes of CO₂, CH₄ and N₂O were investigated for an untreated and a limed soil under beech in open topsoil columns under field conditions for 120 days. Gas fluxes from L. terrestris, beech litter and mineral soil from soil columns were measured separately in jars at 17  °C. The inoculation with L. terrestris and the application of lime had no effect on cumulative CO₂ emissions from soil. During the first 3–4 weeks earthworms significantly (P<0.05) increased CO₂ emissions by 16% to 28%. In contrast, significantly lower (P<0.05) CO₂ emission rates were measured after 11 weeks. The data suggest that earthworm activity was high during the first weeks due to the creation of burrows and incorporation of beech litter into the mineral soil. Low cumulative CH₄ oxidation rates were found in all soil columns as a result of CH₄ production and oxidation processes. L. terrestris with fresh feces and the beech litter produced CH₄ during the laboratory incubation, whereas the mineral soil oxidised atmospheric CH₄. Inoculation with L. terrestris led to a significant reduction (P<0.02) in the CH₄ oxidation rate of soil, i.e. 53% reduction. Liming had no effect on cumulative CH₄ oxidation rates of soil columns and on CH₄ fluxes during the laboratory incubation. L. terrestris significantly increased (P<0.001) cumulative N₂O emissions of unlimed soil columns by 57%. The separate incubation of L. terrestris with fresh feces resulted in rather high N₂O emissions, but the rate strongly decreased from 54 to 2 μg N kg^–1 (dry weight) h^–1 during the 100 h of incubation. Liming had a marked effect on N₂O formation and significantly (P<0.001) reduced cumulative N₂O emissions by 34%. Although the interaction of liming and L. terrestris was not significant, N₂O emissions of limed soil columns with L. terrestris were 8% lower than those of the control. Received: 2 September 1999     

Effect of three contrasting onion (Allium cepa L.) production systems on nitrous oxide emissions from soil

 N₂O emissions were measured from three contrasting onion (Allium cepa L.) production systems over an 8.5-month period. One system was established on soil where a clover sward had 3 months earlier been ploughed in (ploughed clover site). This production system followed conventional production management practices. The other two systems were established on soil where a mixed herb ley had 3 months earlier been either ploughed or rotovated. These last two production systems followed the guidelines of the International Federation of Organic Agriculture Movements (IFOAM). Cumulative N₂O emissions were significantly greater from the ploughed clover site compared to the ploughed ley site (3.8 and 1.6 kg N₂O-N ha^–1, respectively), while cumulative N₂O emissions from the ploughed ley and rotovated ley sites were not significantly different from each other. Emissions from all sites were dominated by episodes of high N₂O flux activity following seedbed preparation and drilling, when soil water suction (SWS) was shown to be the rate-controlling variable. The decline in the N₂O fluxes after these peak emissions followed clear exponential relationships of the form F=Ae^{– kt} (r≥0.91), where F is the daily flux and A is the y-intercept. First-order decay constants (k) during these periods of declining N₂O fluxes (corresponding to half-lives of 2.6–3.0 days) were not significantly different in magnitude from the first-order rate constants that characterised the increasing SWS. Gross differences in cumulative emissions between the clover and ley sites were attributed to the influence of differing soil pHs at the two sites on the N₂O:(N₂O+N₂) ratio in the denitrification products. It also appeared that fertiliser applications to the clover site had both direct and indirect effects on N₂O emissions by: (1) enhancing N₂O emissions via potential nitrification, (2) increasing the NO₃ ^– supply for enhanced N₂O emissions via denitrification, and (3) influencing the N₂O:(N₂O+N₂) ratio by lowering soil pH and increasing NO₃ ^– concentrations. Onion crop yields were greater at the clover site, mainly due to the higher density of planting made possible under a conventional production philosophy. Expressing the yield on the basis of net N₂O emissions, 23 t onions kg^–1 N₂O-N was obtained from the ploughed clover, which was double that obtained for the two systems based on the ley site. However, when the N₂O emissions from the cultivation of the soils prior to the sowing of the onions was included, all three systems produced a similar yield per kilogram of N₂O-N emitted, averaging 10 t kg^–1. Received: 6 January 1999     

Spatial changes of soil fungal and bacterial biomass from a sub-alpine coniferous forest to grassland in a humid, sub-tropical region

 Fungal and bacterial biomass were determined across a gradient from a forest to grassland in a sub-alpine region in central Taiwan. The respiration-inhibition and ergosterol methods for the evaluation of the microbial biomass were compared. Soil fungal and bacterial biomass both significantly decreased (P<0.05) with the shift of vegetation from forest to grassland. Fungal and bacterial respiration rates (evolved CO₂) were, respectively, 89.1 μl CO₂ g^–1 soil h^–1 and 55.1 μl CO₂ g^–1 soil h^–1 in the forest and 36.7 μl CO₂ g^–1 soil h^–1 and 35.7 μl CO₂ g^–1 soil h^–1 in the grassland surface soils (0–10 cm). The fungal ergosterol content in the surface soil decreased from the forest zone (108 μg g^–1) to the grassland zone (15.9 μg g^–1). A good correlation (R ²=0.90) was exhibited between the soil fungal ergosterol content and soil fungal CO₂ production (respiration) for all sampling sites. For the forest and grassland soil profiles, microbial biomass (respiration and ergosterol) declined dramatically with depth, ten- to 100-fold from the surface organic horizon to the deepest mineral horizon. With respect to fungal to bacterial ratios for the surface soil (0–10 cm), the forest zone had a significantly (P<0.05) higher ratio (1.65) than the grassland zone (1.05). However, there was no fungal to bacterial ratio trend from the surface horizon to the deeper mineral horizons of the soil profiles. Received: 30 March 2000     

Effects of nitrogen input and grazing on methane fluxes of extensively and intensively managed grasslands in the Netherlands

 Generally, grasslands are considered as sinks for atmospheric CH₄, and N input as a factor which reduces CH₄ uptake by soils. We aimed to assess the short- and long-term effects of a wide range of N inputs, and of grazing versus mowing, on net CH₄ emissions of grasslands in the Netherlands. These grasslands are mostly intensively managed with a total N input via fertilisation and atmospheric deposition in the range of 300–500 kg N ha^–1 year^–1. Net CH₄ emissions were measured with vented, closed flux chambers at four contrasting sites, which were chosen to represent a range of N inputs. There were no significant effects of grazing versus mowing, stocking density, and withholding N fertilisation for 3–9 years, on net CH₄ emissions. When the ground-water level was close to the soil surface, the injection of cattle slurry resulted in a significant net CH₄ production. The highest atmospheric CH₄ uptake was found at the site with the lowest N input and the lowest ground-water level, with an annual CH₄ uptake of 1.1 kg CH₄ ha^–1 year^–1. This is assumed to be the upper limit of CH₄ uptake by grasslands in the Netherlands. We conclude that grasslands in the Netherlands are a net sink of CH₄, with an estimated CH₄ uptake of 0.5 Gg CH₄ year^–1. At the current rates of total N input, the overall effect of N fertilisation on net CH₄ emissions from grasslands is thought to be small or negligible. Received: 27 January 1998     

Influence of fallow, wheat and subterranean clover on pH within an initially mixed surface soil in the field

 To ascertain the cause of the decrease in pH with depth through the surface 15 cm of moderately acidic soils, pH was monitored in layers of an initially mixed surface soil (to a nominal depth of 10 cm) during two consecutive seasons under fallow, wheat, and subterranean-clover plots. Variation of pH-influencing processes within soil layers to 15 cm depth was measured during the first season. Initially, soil pH was relatively uniform within the surface 7.5 cm, although there was an average 0.53 unit decrease of pH from 0–2.5 cm to 10–15 cm depth. Under all plots, residual lime reaction, net organic anion association and oxidation, net manganese oxidation and reduction, and particularly net N mineralisation and subsequent nitrification, tended to decrease with depth through the surface 15 cm of soil. In wheat and subterranean-clover plots, the alkalinity added with the return of 3.9–4.7 t ha^–1 of plant residue dry matter was predominantly released within the surface 2.5 cm of soil. The dominant pH-influencing processes were net N mineralisation and subsequent nitrification, and the return of alkaline plant residues. In the fallow plots, the surface 10 cm of soil tended to acidify due to nitrification. However in wheat and clover plots, alkalinity added to the surface 2.5 cm of soil from plant residues exceeded acidification resulting from nitrification at this depth. The magnitude of the pH gradient through 0–15 cm depth was therefore maintained under wheat, increased under clover, and decreased under fallow. Received: 11 October 1999     

Methane fluxes and nitrogen dynamics from a drained fenland peat

 Rates of methane uptake were measured in incubation studies with intact cores from adjacent fenland peats that have been under arable management and woodland management for at least the past 30 years. On two separate occasions the woodland peat showed greater rates of uptake than the arable peat. These rates ranged from 23.1 to 223.3 μg CH₄ m^–2 day^–1 for the woodland peat and from 29.6 to 157.6 μg CH₄ m^–2 day^–1 for the arable peat. When the peats were artificially flooded there was a decrease in the rate of methane oxidation, but neither site showed any net efflux of methane. ¹⁵N isotopic dilution was used to characterise nitrogen cycling within the two peats. Both showed similar rates of gross nitrogen mineralisation (3.58 mg N kg^–1 day^–1, arable peat; 3.54 N kg^–1 day^–1, woodland peat) and ammonium consumption (4.19 arable peat and 4.70 mg N kg^–1 day^–1 woodland peat). There were significant differences in their inorganic ammonium and nitrate pool sizes, and the rate of gross nitrification was significantly higher in the woodland peat (4.90 mg N kg^–1 day^–1) compared to the arable peat (1.90 mg N kg^–1 day^–1). These results are discussed in the light of high atmospheric nitrogen deposition. Received: 1 December 1997     

Methane production in a flooded soil in response to elevated atmospheric carbon dioxide concentrations

 CH₄ production in a flooded soil as affected by elevated atmospheric CO₂ was quantified in a laboratory incubation study. CH₄ production in the flooded soil increased by 19.6%, 28.2%, and 33.4% after a 2-week incubation and by 38.2%, 62.4%, and 43.0% after a 3-week incubation under atmospheres of 498, 820, and 1050 μl l^–1 CO₂, respectively, over that in soil under the ambient CO₂ concentration. CH₄ production in slurry under 690, 920, and 1150 μl l^–1 CO₂ increased by 2.7%, 5.5%, and 5.0%, respectively, after a 3-day incubation, and by 6.7%, 12.8%, and 5.4%, respectively, after a 6-day incubation over that in slurry under the ambient CO₂ concentration. The increase in CH₄ production in the soil slurry under elevated CO₂ concentrations in a N₂ atmosphere was more pronounced than that under elevated CO₂ concentrations in air. These data suggested that elevated atmospheric CO₂ concentrations could promote methanogenic activity in flooded soil. Received: 2 March 1998     

Reduced net atmospheric CH4 consumption is a sustained response to elevated CO2 in a temperate forest

We compared, from 2004 through 2006, rates of soil–atmosphere CH₄ exchange at permanently established sampling sites in a temperate forest exposed to ambient (control plots; ∼380 μL L⁻¹) or elevated (ambient + 200 μL L⁻¹) CO₂ since August 1996. A total of 880 observations showed net atmospheric CH₄ consumption (flux from the atmosphere to the soil) from all static chambers most of the time at rates varying from 0.02 mg m⁻² day⁻¹ to 4.5 mg m⁻² day⁻¹. However, we infrequently found net CH₄ production (flux from the soil to the atmosphere) at lower rates, 0.01 mg m⁻² day⁻¹ to 0.08 mg m⁻² day⁻¹. For the entire study, the mean (±SEM) rate of net CH₄ consumption in control plots was higher than the mean for CO₂-enriched plots, 0.55 (0.03) versus 0.51 (0.03) mg m⁻² day⁻¹. Annual rates of 184, 196, and 197 mg m⁻² for net CH₄ consumption at control plots during the three calendar years of this study were 19, 10, and 8% higher than comparable values for CO₂ enriched plots. Differences between treatments were significant in 2004 and 2005 and nearly significant in 2006. Volumetric soil water content was consistently higher at CO₂-enriched sites and a mixed-effects model identified a significant soil moisture x CO₂ interaction on net atmospheric CH₄ consumption. Increased soil moisture at CO₂-enriched sites likely increases diffusional resistance of surface soils and the frequency of anaerobic microsites supporting methanogenesis, resulting in reduced rates of net atmospheric CH₄ consumption. Our study extends our observations of reduced net atmospheric CH₄ consumption at CO₂-enriched plots to nearly five continuous years, suggesting that this is likely a sustained negative feedback to increasing atmospheric CO₂ at this site.     

Urease activity and its relation to soil organic matter, microbial biomass nitrogen and urea-nitrogen assimilation by maize in a Brazilian Oxisol under no-tillage and tillage systems

 We studied the relationship between urease activity (UA) and soil organic matter (SOM), microbial biomass N (N_biom) content, and urea-N fertilizer assimilation by maize in a Dark Red Latosol (Typic Haplustox) cultivated for 9 years under no-tillage (NT), tillage with a disc plough (DP), and tillage with a moldboard plough (MP). Two soil depths were sampled (0–7.5 cm and 7.5–15 cm) at 4 different times during the crop cycle. Urea was applied at four different rates, ranging from 0 to 240 kg N ha^–1. The levels of fertilizer N did not affect the UA, SOM content, and N_biom content. No significant difference between the treatments (NT, DP, and MP) was observed for SOM during the experiment, probably because the major part of the SOM was in recalcitrant pools, since the area was previously cultivated (conventional tillage) for 20 years. The N_biom content explained 97% and 69% of the variation in UA in the upper and deeper soil layer, respectively. UA and biomass N were significantly higher in the NT system compared to the DP and MP systems. The highest maize productivity and urea-N recovery was also observed for the NT system. We observed that the increase in urea-N losses under NT, possibly as a consequence of a higher UA, was compensated for by the increase in N immobilized in the biomass. Received: 2 July 1999     

Soil respiration, nitrogen mineralization and uptake in barley following cultivation of grazed grasslands

 Soil tillage was studied as a strategy to synchronize N mineralization with plant demand following ploughing of two types of grazed pastures [ryegrass/white clover (Lolium perenne/Trifolium repens) and pure ryegrass]. The swards were either rotovated and ploughed or ploughed only. Soil respiration, as determined by a dynamic chamber method, was related to net N mineralization and to plant N uptake in a subsequent spring barley crop (Hordeum vulgare). Diurnal variations in temperature were important for the CO₂ flux and care must be taken that temperatures during measuring periods are representative of the daily mean. Soil tillage increased the CO₂ flux considerably compared with untilled soil with total emissions of 2.6 and 1.4 t C ha^–1, respectively, from start of April to end of June. Sward type or rotovation did not markedly influence accumulated emissions. Rotovation significantly increased the content of nitrate in the soil until 43 days after rotovation, showing that net N mineralization occurred rapidly during this period, in spite of low soil temperatures (5–10  °C). Rotovation increased barley grain yield by 10–12% and N-uptake by 14%. For both sward types, rotovation caused an extra N-uptake in harvested plant material of about 12 kg ha^–1. The availability of soil inorganic N at the early stages of barley was important for the final yield and N-uptake. The results indicated that soil biological activity was not enhanced by rotovation and that the yield effect of rotovation was mainly caused by quicker availability and better synchrony between N mineralization and plant uptake due to earlier start of decomposition. Received: 3 May 2000     

EFFECTS OF CULTIVATION ON SOIL WATER RETENTION AND WATER USE BY CEREALS IN CLAY SOILS

The effects are repotted of direct drilling and mouldboard ploughing on soil water retention and extraction in three soils over two to four years. In the years 1972–75 when winter rainfall was close to or greater than the long-term average the maximum soil water content of the upper 100 cm differed little between the cultivation treatments. In contrast, after the dry winter of 1975–76, about 10 per cent more water was stored in the direct-drilled soil, especially below 50 cm. In the following dry summer, winter wheat extracted up to 22 mm more water from uncultivated soil and this was associated with better growth of the crop than after ploughing. When simulated rain was applied, water infiltrated rapidly to a depth of 50–100 cm in direct-drilled soil, whereas on ploughed land its movement was retarded below the plough sole even when cultivation had been carried out under conditions which minimized smearing. Water storage at depth was consequently greater under dry conditions in the direct-drilled soil while excess water reached drain depth more rapidly in wet conditions.     

Effect of temperature on reduction of iron and production of carbon dioxide and methane in anoxic wetland rice soils

 Wetland rice soils from Italy (Pavia) and the Philippines (Bugallon, Luisiana, Maligaya) were incubated under anoxic conditions at 31 different temperatures ranging from 4.7  °C to 49.5  °C. Production of CO₂ was most intensive at the beginning of the incubation (0–4 days) and was predominantly coupled to the reduction of free Fe(III). The optimum temperature for these processes was between 32  °C and 41  °C. After 9–16 days, CO₂ production rates had decreased and the available Fe(III) had been completely reduced at the optimum temperatures. However, Fe(III) was still available at temperatures below and above the optimum. Maximum CH₄ production rates were observed after 4–16 days (except in soil from Maligaya) with temperature optima between 32  °C and 41  °C, similar to those for CO₂ production and Fe reduction. Since ongoing Fe reduction is known to suppress CH₄ production, the temperature range of optimum CH₄ production was restricted to those temperatures at which Fe(III) had already been depleted. Nevertheless, the temperature characteristics of both CO₂ and CH₄ production often exhibited two temperature optima at some time during the incubation, suggesting a complex pattern of adaptation of the methanogenic microbial community to temperature. When available Fe(III) was completely depleted by anoxic pre-incubation at 30  °C, CH₄ was produced at a constant rate (steady state conditions) which increased with increasing temperature. Steady state CH₄ production reached a first maximum at about 40  °C, but increased further up to at least 50  °C, suggesting the presence of thermophilic microorganisms whose activity was apparently masked when Fe had not been completely reduced. The apparent activation energy of CH₄ production at steady state ranged between 48 kJ mol^–1 and 65 kJ mol^–1. Received: 26 August 1999