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.     

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     

Effects of climatic factors and soil management on the methane flux in soils from annual and perennial energy crops

Methane flux rates were measured on a loamy sand soil within perennial and annual energy crops in northeast Germany. The study was performed in closed chambers between 2003 and 2005 with four measurements per week. A mixed linear model including the fixed effects of year, rotation period, crop and fertilisation was applied to determine the influence of climatic factors and soil management on the CH₄ flux. Soil water content and air temperature were added as co-variables. With the exception of air temperature, all fixed effects and the co-variable soil water content influenced the CH₄ flux. The soil of annual crops consumed 6.1 μg CH₄ m⁻² h⁻¹, significantly more than the soil of perennial crops with 4.3 μg CH₄ m⁻² h⁻¹. It is suggested that soil water content plays the key role in CH₄ flux between pedosphere and atmosphere. In the range of water contents between 5% and 15%, our model describes that a soil water content increase of 1% induces a net emission of 0.375 μg CH₄ m⁻² h⁻¹. As the soil of the experimental field was well-drained and aerobic, it represented a net sink for CH₄ throughout the study period.     

Crop residues and fertilizer nitrogen influence residue decomposition and nitrous oxide emission from a Vertisol

Crop residues with high C/N ratio immobilize N released during decomposition in soil, thus reducing N losses through leaching, denitrification, and nitrous oxide (N₂O) emission. A laboratory incubation experiment was conducted for 84 days under controlled conditions (24°C and moisture content 55% of water-holding capacity) to study the influence of sugarcane, maize, sorghum, cotton and lucerne residues, and mineral N addition, on N mineralization–immobilization and N₂O emission. Residues were added at the rate of 3 t C ha⁻¹ to soil with, and without, 150 kg urea N ha⁻¹. The addition of sugarcane, maize, and sorghum residues without N fertilizer resulted in a significant immobilization of soil N. Amended soil had significantly (P < 0.05) lower NO₃⁻–N, which reached minimum values of 2.8 mg N kg⁻¹ for sugarcane (at day 28), 10.3 mg N kg⁻¹ for maize (day 7), and 5.9 mg N kg⁻¹ for sorghum (day 7), compared to 22.7 mg N kg⁻¹ for the unamended soil (day 7). During 84 days of incubation, the total mineral N in the residues + N treatments were decreased by 45 mg N kg⁻¹ in sugarcane, 34 mg kg⁻¹ in maize, 29 mg kg⁻¹ in sorghum, and 16 mg kg⁻¹ in cotton amended soil compared to soil + N fertilizer, although soil NO₃⁻–N increased by 7 mg kg⁻¹ in lucerne amended soil. The addition of residues also significantly increased amended soil microbial biomass C and N. Maximum emissions of N₂O from crop residue amended soils occurred in the first 4–5 days of incubation. Overall, after 84 days of incubation, the cumulative N₂O emission was 25% lower with cotton + N fertilizer, compared to soil + N fertilizer. The cumulative N₂O emission was significantly and positively correlated with NO₃⁻–N (r = 0.92, P < 0.01) and total mineral N (r = 0.93, P < 0.01) after 84 days of incubation, and had a weak but significant positive correlation with cumulative CO₂ in the first 3 and 5 days of incubation (r = 0.59, P < 0.05).     

Emissions of CO2, CH4 and N2O from Southern European peatlands

Peatlands play an important role in emissions of the greenhouse gases CO₂, CH₄ and N₂O, which are produced during mineralization of the peat organic matter. To examine the influence of soil type (fen, bog soil) and environmental factors (temperature, groundwater level), emission of CO₂, CH₄ and N₂O and soil temperature and groundwater level were measured weekly or biweekly in loco over a one-year period at four sites located in Ljubljana Marsh, Slovenia using the static chamber technique. The study involved two fen and two bog soils differing in organic carbon and nitrogen content, pH, bulk density, water holding capacity and groundwater level. The lowest CO₂ fluxes occurred during the winter, fluxes of N₂O were highest during summer and early spring (February, March) and fluxes of CH₄ were highest during autumn. The temporal variation in CO₂ fluxes could be explained by seasonal temperature variations, whereas CH₄ and N₂O fluxes could be correlated to groundwater level and soil carbon content. The experimental sites were net sources of measured greenhouse gases except for the drained bog site, which was a net sink of CH₄. The mean fluxes of CO₂ ranged between 139 mg m⁻² h⁻¹ in the undrained bog and 206 mg m⁻² h⁻¹ in the drained fen; mean fluxes of CH₄ were between −0.04 mg m⁻² h⁻¹ in the drained bog and 0.05 mg m⁻² h⁻¹ in the drained fen; and mean fluxes of N₂O were between 0.43 mg m⁻² h⁻¹ in the drained fen and 1.03 mg m⁻² h⁻¹ in the drained bog. These results indicate that the examined peatlands emit similar amounts of CO₂ and CH₄ to peatlands in Central and Northern Europe and significantly higher amounts of N₂O.     

Changes in CO<Subscript>2</Subscript>, <Superscript>13</Superscript>C abundance,inorganic nitrogen, β-glucosidase,and oxidative enzyme activities of soil during the decomposition of switchgrass root carbon as affected by inorganic nitrogen additions

This study was conducted to investigate the effect of inorganic nitrogen (N) and root carbon (C) addition on decomposition of organic matter (OM). Soil was incubated for 200 days with nine treatments (three levels of N (no addition (N0) = 0, low N (NL) = 0.021, high N (NH) = 0.083 mg N g⁻¹ soil) × three levels of C (no addition (C0) = 0, low C (CL) = 5, high C (CH) = 10 mg root g⁻¹ soil)). The carbon dioxide (CO₂) efflux rates, inorganic N concentration, pH, and potential activities of β-glucosidase and oxidative enzyme were measured during incubation. At the beginning and the end of incubation, the native soil organic carbon (SOC) and root-derived SOC were quantified by using a natural labeling technique based on the differences in δ ¹³C between C3 and C4 plants. Overall, the interaction between C and N was not significant. The decomposition of OM in the NH treatment decreased. This could be attributed to the formation of recalcitrant OM by N because the potentially mineralizable C pool was significantly lower in the NH treatment (3.1 mg C g⁻¹) than in the N0 treatment (3.6 mg C  g⁻¹). In root C addition treatments, the CO₂ efflux rate was generally in order of CH > CL > C0 over the incubation period. Despite no differences in the total SOC concentration among C treatments, the native SOC in the CH treatment (18.29 mg C g⁻¹) was significantly lower than that in the C0 treatment (19.16 mg C g⁻¹).     

Methane concentrations and methanotrophic community structure influence the response of soil methane oxidation to nitrogen content in a temperate forest

Methane oxidation in forest soils removes atmospheric CH₄. Many studies have determined methane uptake rates and their controlling variables, yet the microorganisms involved have rarely been assessed simultaneously over the longer term. We measured methane uptake rates and the community structure of methanotrophic bacteria in temperate forest soil (sandy clay loam) on a monthly basis for two years in South Korea. Methane uptake rates at the field site did not show any seasonal patterns, and net uptake occurred throughout both years. In situ uptake rates and uptake potentials determined in the laboratory were 2.92 ± 4.07 mg CH₄ m⁻² day⁻¹ and 51.6 ± 45.8 ng CH₄ g⁻¹ soil day⁻¹, respectively. Contrary to results from other studies, in situ oxidation rates were positively correlated with soil nitrate concentrations. Short-term experimental nitrate addition (0.20-1.95 μg N g⁻¹ soil) significantly stimulated oxidation rates under low methane concentrations (1.7-2.0 ppmv CH₄), but significantly inhibited oxidation under high methane concentrations (300 ppmv CH₄). We analyzed the community structures of methanotrophic bacteria using a DNA-based fingerprinting method (T-RFLP). Type II methanotrophs dominated under low methane concentrations while Type I methanotrophs dominated under high methane concentrations. Nitrogen addition selectively inhibited Type I methanotrophic bacteria. Overall, the results of this study indicate that the effects of inorganic N on methane uptake depend on methane concentrations and that such a response is related to the dissimilar activation or inhibition of different types of methanotrophic bacteria.     

Nitrate and Phosphate Leaching under Turfgrass Fertilized with a Squid-based Organic Fertilizer

Consumer demand for cleaned squid generates a substantial amount of waste that must be properly disposed of, creating an economic burden on processors. A potential solution to this problem involves converting squid by-products into an organic fertilizer, for which there is growing demand. Because fertilizer application to lawns can increase the risk of nutrient contamination of groundwater, we quantified leaching of NO₃–N and PO₄–P from perennial ryegrass turf (Lolium perenne L.) amended with two types of fertilizer: squid-based (SQ) and synthetic (SY). Field plots were established on an Enfield silt loam, and liquid (L) and granular (G) fertilizer formulations of squid and synthetic fertilizers were applied at 0, 48, 146, and 292 kg N ha⁻¹ year⁻¹. Levels of NO₃–N and PO₄–P in soil pore water from a depth of 60 cm were determined periodically during the growing season in 2008 and 2009. Pore water NO₃–N levels were not significantly different among fertilizer type or formulation within an application rate throughout the course of the study. The concentration of NO₃–N remained below the maximum contaminant level (MCL) of 10 mg L⁻¹ until midSeptember 2009, when values above the MCL were observed for SQG at all application rates, and for SYL at the high application rate. Annual mass losses of NO₃–N were below the estimated inputs (10 kg N ha⁻¹ year⁻¹) from atmospheric deposition except for the SQG and SYL treatments applied at 292 kg N ha⁻¹ year⁻¹, which had losses of 13.2 and 14.9 kg N ha⁻¹ year⁻¹, respectively. Pore water PO₄–P levels ranged from 0 to 1.5 mg P L⁻¹ and were not significantly different among fertilizer type or formulation within an application rate. Our results indicate that N and P losses from turf amended with squid-based fertilizer do not differ from those amended with synthetic fertilizers or unfertilized turf. Although organic in nature, squid-based fertilizer does not appear to be more—or less—environmentally benign than synthetic fertilizers.     

Effects of moisture and temperature on greenhouse gas emissions and C and N leaching losses in soil treated with biogas slurry

The objective of this study was to examine the effects of soil moisture, irrigation pattern, and temperature on gaseous and leaching losses of carbon (C) and nitrogen (N) from soils amended with biogas slurry (BS). Undisturbed soil cores were amended with BS (33 kg N ha⁻¹) and incubated at 13.5°C and 23.5°C under continuous irrigation (2 mm day⁻¹) or cycles of strong irrigation and partial drying (every 6 weeks, 1 week with 12 mm day⁻¹). During the 6 weeks after BS application, on average, 30% and 3.8% of the C and N applied with BS were emitted as carbon dioxide (CO₂) and nitrous oxide (N₂O), respectively. Across all treatments, a temperature increase of 10°C increased N₂O and CO₂ emissions by a factor of 3.7 and 1.7, respectively. The irrigation pattern strongly affected the temporal production of CO₂ and N₂O but had no significant effect on the cumulative production. Nitrogen was predominantly lost in the form of nitrate (NO₃⁻). On average, 16% of the N applied was lost as NO₃⁻. Nitrate leaching was significantly increased at the higher temperature (P < 0.01), while the irrigation pattern had no effect (P = 0.63). Our results show that the C and N turnovers were strongly affected by BS application and soil temperature whereas irrigation pattern had only minor effects. A considerable proportion of the C and N in BS were readily available for soil microorganisms.     

Nitrogen mineralization and CO2 and N2O emissions in a sandy soil amended with original or acidified pig slurries or with the relative fractions

The following six pig slurries obtained after acidification and/or solid/liquid separation were used in the research: original (S) and acidified (AS) pig slurry, nonacidified (LF) and acidified (ALF) pig slurry liquid fraction, and nonacidified (SF) and acidified (ASF) pig slurry solid fraction. Laboratory incubations were performed to assess the effect of the application of these slurries on N mineralization and CO₂ and N₂O emissions from a sandy soil. Acidification maintained higher NH₄ ⁺-N contents in soil particularly in the ALF-treated soil where NH₄ ⁺-N contents were two times higher than in LF-treated soil during the 55–171-day interval. At the end of the incubation (171 days), 32.9 and 24.2 mg N kg⁻¹ dry soil were mineralized in the ASF- and SF-treated soils, respectively, but no mineralization occurred in LF- and S-treated soils, although acidification decreased N immobilization in ALF- (−25.3 mg N kg⁻¹ soil) and AS- (−12.7 mg N kg⁻¹ soil) compared to LF- (−34.4 mg N kg⁻¹ soil) and S-treated (−18.6 mg N kg⁻¹ soil) soils, respectively. Most of the dissolved CO₂ was lost during the acidification process. More than 90% of the applied C in the LF-treated soil was lost during the incubation, indicating a high availability of the added organic compounds. Nitrous oxide emissions occurred only after day 12 and at a lower rate in soils treated with acidified than nonacidified slurries. However, during the first 61 days of incubation, 1,157 μg N kg⁻¹ soil was lost as N₂O in the AS-treated soil and only 937 in the S-treated soil.     

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     

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     

Secondary salinity effects on soil microbial biomass

Secondary soil salinilization is a big problem in irrigated agriculture. We have studied the effects of irrigation-induced salinity on microbial biomass of soil under traditional cotton (Gossypium hirsutum L.) monoculture in Sayhunobod district of the Syr-Darya province of northwest Uzbekistan. Composite samples were randomly collected at 0–30 cm depth from weakly saline (2.3 ± 0.3 dS m⁻¹), moderately saline (5.6 ± 0.6 dS m⁻¹), and strongly saline (7.1 ± 0.6 dS m⁻¹) replicated fields, 2-mm sieved, and analyzed for pH, electrical conductivity, total C, organic C (C_Org), and extractable C, total N and P, and exchangeable ions (Ca²⁺, Mg²⁺, K⁺, Na⁺, Cl⁻, and CO₃²⁻), microbial biomass (C_mic). The Na⁺ and Cl⁻ concentrations were 36-80% higher in strongly saline compared to weakly saline soil. The C_Org concentration was decreased by 10% and C_Ext by 40% by increasing soil salinity, whereas decrease in C_mic ranged from 18-42% and the percentage of C_Org present as C_mic from 8% to 26%. We conclude that irrigation-induced secondary salinity significantly affects soil chemical properties and the size of soil microflora.     

Effects of long-term exposure to enriched CO<Subscript>2</Subscript> on the nutrient-supplying capacity of a grassland soil

Altered soil nutrient cycling under future climate scenarios may affect pasture production and fertilizer management. We conducted a controlled-environment study to test the hypothesis that long-term exposure of pasture to enriched carbon dioxide (CO₂) would lower soil nutrient availability. Perennial ryegrass was grown for 9 weeks under ambient and enriched (ambient + 120 ppm) CO₂ concentrations in soil collected from an 11.5-year free air CO₂ enrichment experiment in a grazed pasture in New Zealand. Nitrogen (N) and phosphorus (P) fertilizers were applied in a full factorial design at rates of 0, 12.5, 25 or 50 kg N ha⁻¹ and 0, 17.5 or 35 kg P ha⁻¹. Compared to ambient CO₂, under enriched CO₂ without P fertilizer, total plant biomass did not respond to N fertilizer, and tissue N/P ratio was increased indicating that P was co-limiting. This limitation was alleviated with the lowest rate of P fertilizer (17.5 kg P ha⁻¹). Plant biomass in both CO₂ treatments increased with increasing N fertilizer when sufficient P was available. Greater inputs of P fertilizer may be required to prevent yield suppression under enriched CO₂ and to stimulate any response to N.     

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     

Short-term decomposition of <Superscript>14</Superscript>C-labelled glucose in a fluvo-aquic soil as affected by lanthanum amendment

In this study, we investigated the effects of lanthanum (La), one of the rare earth elements (REEs), on microbial biomass C as well as the decomposition of ¹⁴C-labelled glucose in a fluvo-aquic soil in 28 days. The soil was collected from the field plots under maize/wheat rotation in Fengqiu Ecological Experimental Station of Chinese Academy of Sciences, Henan Province, China. Application of La decreased soil microbial biomass C during the experimental period, and there was a negative correlation (P < 0.01) between microbial biomass and application rate of La. La increased microbial biomass ¹⁴C after ¹⁴C glucose addition, and the increase was significant (P < 0.05) at the rates of more than 160 mg kg⁻¹ soil. La slightly increased ¹⁴CO₂ evolution at lower rates of application but decreased it at higher rates 1 day after ¹⁴C glucose addition, while there was no significant effect from days 2 to 28. For the cumulative ¹⁴CO₂ evolution during the incubation of 28 days, La slightly increased it at the rates of less than 120 mg kg⁻¹ soil, while significantly decreased (P < 0.05) it at the rate of 200 mg kg⁻¹ soil. The results indicated that agricultural use of REEs such as La in soil could decrease the amount of soil microbial biomass and change the pattern of microbial utilization on glucose C source in a short period.     

Carbon and nitrogen mineralization dynamics in different soils of the tropics amended with legume residues and contrasting soil moisture contents

Seasonal drought in tropical agroecosystems may affect C and N mineralization of organic residues. To understand this effect, C and N mineralization dynamics in three tropical soils (Af, An₁, and An₂) amended with haricot bean (HB; Phaseolus vulgaris L.) and pigeon pea (PP; Cajanus cajan L.) residues (each at 5 mg g⁻¹ dry soil) at two contrasting soil moisture contents (pF2.5 and pF3.9) were investigated under laboratory incubation for 100–135 days. The legume residues markedly enhanced the net cumulative CO₂–C flux and its rate throughout the incubation period. The cumulative CO₂–C fluxes and their rates were lower at pF3.9 than at pF2.5 with control soils and also relatively lower with HB-treated than PP-treated soil samples. After 100 days of incubation, 32–42% of the amended C of residues was recovered as CO₂–C. In one of the three soils (An₁), the results revealed that the decomposition of the recalcitrant fraction was more inhibited by drought stress than easily degradable fraction, suggesting further studies of moisture stress and litter quality interactions. Significantly (p < 0.05) greater NH₄⁺–N and NO₃⁻–N were produced with PP-treated (C/N ratio, 20.4) than HB-treated (C/N ratio, 40.6) soil samples. Greater net N mineralization or lower immobilization was displayed at pF2.5 than at pF3.9 with all soil samples. Strikingly, N was immobilized equivocally in both NH₄⁺–N and NO₃⁻–N forms, challenging the paradigm that ammonium is the preferred N source for microorganisms. The results strongly exhibited altered C/N stoichiometry due to drought stress substantially affecting the active microbial functional groups, fungi being dominant over bacteria. Interestingly, the results showed that legume residues can be potential fertilizer sources for nutrient-depleted tropical soils. In addition, application of plant residue can help to counter the N loss caused by leaching. It can also synchronize crop N uptake and N release from soil by utilizing microbes as an ephemeral nutrient pool during the early crop growth period.     

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     

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     

Short-term effects of clearfelling on soil CO2, CH4, and N2O fluxes in a Sitka spruce plantation

We examined the effects of forest clearfelling on the fluxes of soil CO₂, CH₄, and N₂O in a Sitka spruce (Picea sitchensis (Bong.) Carr.) plantation on an organic-rich peaty gley soil, in Northern England. Soil CO₂, CH₄, N₂O as well as environmental factors such as soil temperature, soil water content, and depth to the water table were recorded in two mature stands for one growing season, at the end of which one of the two stands was felled and one was left as control. Monitoring of the same parameters continued thereafter for a second growing season. For the first 10 months after clearfelling, there was a significant decrease in soil CO₂ efflux, with an average efflux rate of 4.0 g m⁻² d⁻¹ in the mature stand (40-year) and 2.7 g m⁻² d⁻¹ in clearfelled site (CF). Clearfelling turned the soil from a sink (−0.37 mg m⁻² d⁻¹) for CH₄ to a net source (2.01 mg m⁻² d⁻¹). For the same period, soil N₂O fluxes averaged 0.57 mg m⁻² d⁻¹ in the CF and 0.23 mg m⁻² d⁻¹ in the 40-year stand. Clearfelling affected environmental factors and lead to higher daily soil temperatures during the summer period, while it caused an increase in the soil water content and a rise in the water table depth. Despite clearfelling, CO₂ remained the dominant greenhouse gas in terms of its greenhouse warming potential.