Ethylene oxidation,atmospheric methane consumption,and ammonium oxidation in temperate volcanic forest soils

Temperate volcanic forest surface soils under different forest stands (e.g., Pinus sylvestris L., Cryptomeria japonica, and Quercus serrata) were sampled to study the kinetics of ethylene (C₂H₄) oxidation and the C₂H₄ concentrations that effectively inhibit oxidation of atmospheric methane (CH₄) and nitrification. The kinetics of C₂H₄ oxidation in temperate volcanic forest soils was biphasic, indicating that at least two different microbial populations, one with low and another with high apparent K _m values, were responsible for ethylene oxidation. Methane consumption activity and ammonium oxidation of soil were inhibited by adding ethylene. Added C₂H₄ at concentrations of 3, 10, and 20 μl C₂H₄ per liter in the headspace gas respectively reduced by 20%, 50%, and 100% atmospheric CH₄ consumption by soil, and these values were much smaller than those inhibiting ammonium oxidation in these forest soils; thus, the CH₄ consumption activity was more sensitive to the addition of C₂H₄ than ammonium oxidation. Previous studies have shown that accumulation of C₂H₄ in such volcanic forest soils within 3 days of aerobic and anaerobic incubations can reach a range from 0.2 to 0.3 and from 1.0 to 3.0 μl C₂H₄ per liter in the headspace gas, respectively. It is suggested that C₂H₄ production beneath forest floors, particularly after heavy rain, can to some extent affect the capacity of forest surface soils to consume atmospheric CH₄, but probably, it has no impact on ammonium oxidation.     

Methane oxidation in temperate soils: effects of inorganic N

Additions of inorganic nitrogen (N) to an oak soil with significant potential for methane (CH₄) oxidation resulted in differential reduction in CH₄ oxidation capacity depending on N species added. Nitrate, rather than nitrite or ammonium, proved to be the strongest inhibitor of CH₄ oxidation in oak soil. Both high (CH₄ at 10 μl l⁻¹) and low (CH₄ at 5 ml l⁻¹) affinity CH₄ oxidation in oak soil was completely inhibited at a nitrate concentration similar to that present in an alder soil from the same experimental site. The alder soil showed no capacity for low affinity CH₄ oxidation. A ‘low nitrate’ forest soil (oak) showed high affinity, low capacity CH₄ oxidation upto around 1 ml l⁻¹ CH₄, above which both high and low affinity CH₄ oxidation became apparent following a lag phase, indicating either an induced high affinity uptake mechanism or the existence of distinct low affinity and high affinity methanotroph populations. High affinity CH₄ oxidation became saturated at CH₄ concentrations >500 μl l⁻¹, while low affinity CH₄ oxidation became saturated at ∼30 ml l⁻¹ CH₄. In a ‘high nitrate’ forest soil (alder), CH₄ oxidation appeared to be due to high affinity CH₄ oxidation only and became undetectable at CH₄ concentrations >5 ml l⁻¹.     

Water-soluble Al inhibits methane oxidation at atmospheric concentration levels in Japanese forest soil

The effect of aluminium on methane oxidation was examined from incubation experiments involving the addition of several concentrations of Al solution (0.1, 0.2, 0.5, 1, 3 and 5 mM) to two soil samples that possessed different CH₄ oxidation potential. Atmospheric CH₄ oxidation activity was inhibited by the addition of as little as 0.1 mM Al solution (approximately 0.5 μg of Al per gram dry weight soil) to a forest soil that contained low water-soluble Al and possessed a high CH₄ oxidation potential. Our results indicate that Al inhibition of CH₄ oxidation activity is concentration-dependant after a certain time and the inhibition increases gradually over time until at least 96 h have elapsed. We also found that relatively small amounts of Al additions, such as 10-20 μg per gram dry weight of soil, halved the CH₄ oxidation rate compared to the control, regardless of the original CH₄ oxidation potential of the soil. Since the Al concentrations used in our experiment are often observed in forest soils, we can assume that Al acts as an important inhibitor of CH₄ oxidation in forest soils under natural conditions. The sharp falls and a continuous decrease in CH₄ oxidation rate in other forest samples with the addition of deionized water implies that the water-soluble Al contained in soils contributes to the inhibition of CH₄ oxidation rate. This result suggests that precipitation causes a relatively prolonged inhibition of CH₄ oxidation in soils containing a high concentration of water-soluble Al.     

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.     

Temporal variation in pools of amino acids, inorganic and microbial N in a temperate grassland soil

Plants can take up intact amino acids, even in competition with soil microbes, yet we lack detailed information on which amino acids dominate the soil and whether amino acid composition varies seasonally. This study tested the hypotheses that 1) the pool of amino acid N is generally larger than inorganic N; 2) temporal changes in the concentration of amino acid N is related to changes in the size of the microbial N pool; and 3) amino acid N is dominated by simple, neutral amino acids during warm months, whereas during cold months the amino acid N is dominated by more complex aromatic and basic amino acids. Approximately every month for two years we collected soil from a temperate, sub-alpine grassland in the Snowy Mountains of Australia. We quantified exchangeable pools of amino acids, nitrate and ammonium in 1 M KCl extracts. Microbial N was quantified by chloroform fumigation. Averaged across the 21 monthly samples, nitrate was 13% of the quantified pool of soluble non-protein N, ammonium was 34% and amino acid N was 53%. These data are consistent with our hypothesis that the pool of amino acid N is larger than inorganic N. There was substantial variation between months in concentrations of amino acids and inorganic N, but no clear temporal pattern. Microbial N did not vary between months, and thus changes in amino acid N were unrelated to microbial N. Principal components analysis indicated multivariate groupings of the different pools of N that were broadly indicative of function and/or biosynthetic relationships. Thus PCA identified a grouping of aromatic amino acids (Phe and Try) with amino acids derived from oxaloacetate (Asp, Ala, Val, Leu, Ile), and a second group comprising microbial N, nitrate and glycine. The pool of exchangeable amino acid N was dominated by Arg (26% of amino N) Val (20%) Gln (18%), Try (8%) and Asn (8%). Contrary to our hypothesis, the composition of the amino acid pool did not vary in a consistent way between months, and there was no evidence simple amino acids were relatively more abundant in warm months and complex amino acids in cool months.     

Effects of N sources and methane concentrations on methane uptake potential of a typical coniferous forest and its adjacent orchard soil

After removal of the above-ground plant debris three different soil layers were taken from a typical coniferous forest and its adjacent orchard in Numata City, Japan. The potentials of soil CH₄ uptake at two initial CH₄ concentrations were studied under aerobic conditions in the laboratory, along with inhibition of soil CH₄ oxidation by urea-N or KNO₃-N addition. Due to long-term N inputs, the CH₄ uptake of the upper mineral layer of the orchard soil was 25.4% and 87.7% lower than that of the surface forest soil at 2.4 and 12.6 l l^–1 CH₄, respectively. Methane uptake of the forest soil decreased with increasing soil depths at two CH₄ levels. However, maximal CH₄-consuming activity occurred in the 9- to 23-cm depth of the orchard soil at 12.6 l l^–1 methane. Nitrogen additions in the form of KNO₃ or urea at the rate of 200 g N g^–1 soil substantially reduced soil CH₄ uptake in the upper and sub-surface mineral layers at both sites, except that the addition of KNO₃-N had no apparent inhibitory effect on the CH₄ uptake in the 9- to 23-cm depth of the orchard soil. A strong inhibitory effect of NO₃^– addition on the CH₄ uptake, in contrast to NH₄⁺, occurred in the surface forest soil. The use of KNO₃-N, as compared to urea or urea plus a nitrification inhibitor (dicyandiamide), resulted in a lower potential to cause inhibition of CH₄ oxidation in the 0- to 23-cm depth of the orchard soil.     

Dimethyl sulphoxide (DMSO) and dimethyl sulphide (DMS) as inhibitors of methane oxidation in forest soil

Dimethyl sulphoxide (DMSO) at 14 mM inhibits CH₄ oxidation in forest soil, but the inhibition mechanism is unknown. When soil slurries are incubated in gas tight flasks, there is a lag of about 45 h before DMSO inhibits CH₄ oxidation. We tried to determine if some metabolic compound derived from DMSO, as a result of microbial activity, is responsible for the inhibition. Dimethyl sulphide (DMS) accumulated in the sealed flasks up to 5-83 μl l⁻¹ in the headspace during a 2-week period. DMS at 1 μl l⁻¹ in the headspace (0.64 μM in soil-water slurry) had a negligible effect on CH₄ oxidation but 50 μl l⁻¹ DMS (32 μM) inhibited CH₄ oxidation completely. However, the inhibition by DMSO was already evident after 45 h, when DMS concentrations were generally non-inhibiting (0.1-0.7 μl l⁻¹). DMSO was also shown to inhibit CH₄ oxidation when the DMS produced was continuously removed. Results suggest that the production of DMS from DMSO makes a minor contribution to the inhibition of CH₄ oxidation by DMSO with incubation times relevant in CH₄ oxidation studies.     

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     

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     

施用铵态氮对森林土壤硝态氮和铵态氮的影响

对取自武夷山的红壤、黄壤、黄壤性草甸土分别在对照(CK,N 0 mg/kg)、低氮(LN,N 50 mg/kg)、高氮(HN,N 100 mg/kg)3种氮(N)水平处理下开展培养实验,研究施加NH4+-N对森林土壤N转化的短期影响.结果表明,添加NH4+-N可显著(p＜0.05)降低土壤NO3--N含量4.5％～25.7％,但LN与HN处理差异不显著,NO3--N降低可能与NO3--N反硝化和异氧还原有关;然而,黄壤性草甸土NO3--N没有降低.与培养前比较,在第56天红壤NO3--N含量显著增加5倍左右;桐木关黄壤增加40％左右,而黄冈山25 km黄壤仅在CK处理下增加16％,但是黄壤性草甸土显著降低;结果显示LN与HN处理土壤NO3--N含量变化幅度小于CK.与CK相比,LN和HN处理红壤NH4+-N分别显著(p＜0.05)升高24.1％ ～ 96.5％和68.7％～114.1％,且随培养进行没有累积,可能与微生物固N有关;桐木关NH4+-N分别升高17.6％ ～ 39.6％和37.6％～95.8％ (p＜0.05),LN处理黄冈山25 km黄壤NH4+-N只有第7天升高17.8％ (p＜0.05),HN处理第7、14、28、42天显著升高17.5％～48.6％(p＜0.05).LN处理黄壤性草甸土的NH4+-N在前3周显著降低11.6％～28.5％ (p＜0.01); HN处理在第7天和14天分别降低10.8％(p＜0.01)和7.5％,但是在第28～56天显著增加17.6％～20.4％(p=0.002).随着培养进行,CK处理红壤NH4+-N逐渐降低,桐木关黄壤、黄冈山25 km黄壤和黄壤性草甸土升高;LN和HN处理黄壤和黄壤性草甸土NH4+-N逐渐升高.可见,不同海拔土壤类型对NH4+-N添加响应存在差异.     

Methane oxidation in boreal forest soils: kinetics and sensitivity to pH and ammonium

In soil incubation experiments we examined if there are differences in the kinetic parameters of atmospheric methane (CH₄) oxidation in soils of upland forests and forested peatlands. All soils showed net uptake of atmospheric CH₄. One of the upland forests included also managed (clear-cut with or without previous liming or N-fertilization) study plots. The CH₄ oxidation in the forested peat soil had a higher K_m (510 μl l⁻¹) and V_max (6.2 nmol CH₄ cm⁻³ h⁻¹) than the upland forest soils (K_m from 5 to 18 μl l⁻¹ and V_max from 0.15 to 1.7 nmol CH₄ cm⁻³ h⁻¹). The forest managements did not affect the K_m-values. At atmospheric CH₄ concentration, the upland forest soils had a higher CH₄ oxidation activity than the forested peat soil; at high CH₄ concentrations the reverse was true. Most of the soils oxidised CH₄ in the studied pH range from 3 to 7.5. The pH optimum for CH₄ oxidation varied from 4 to 7.5. Some of the soils had a pH optimum for CH₄ oxidation that was above their natural pH. The CH₄ oxidation in the upland forest soils and in the peat soil did not differ in their sensitivities to (NH₄)₂SO₄ or K₂SO₄ (used as a non-ammonium salt control). Inhibition of CH₄ oxidation by (NH₄)₂SO₄ resulted mainly from a general salt effect (osmotic stress) though NH₄⁺ did have some additional inhibitory properties. Both salts were better inhibitors of CH₄ oxidation than respiration. The differences in the CH₄ oxidation kinetics in the forested peat soil and in the upland forest soils reveal that there are differences in the physiologies of the CH₄ oxidisers in these soils.     

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     

Methane oxidation in arable soil as inhibited by ammonium, nitrite, and organic manure with respect to soil pH

 The effects of inorganic N and organic manure, applied to a loamy arable soil, on CH₄ oxidation were investigated in laboratory incubation experiments. Applications (40 mg N kg^–1) of NH₄Cl, (NH₄)₂SO₄, and urea caused strong instantaneous inhibition of CH₄ oxidation by 96%, 80%, and 84%, respectively. After nitrification of the added N the inhibitory effect was not fully reversible, resulting in an residual inhibition of 21%, 16%, and 25% in the NH₄Cl, (NH₄)₂SO₄, and urea treatments, respectively. With large NH₄ ⁺ applications [240 mg N kg^–1 as (NH₄)₂SO₄] the residual inhibition was as high as 64%. Exogenous NO₂ ^– (40 mg NO₂ ^–-N kg^–1) initially inhibited CH₄ oxidation by 84%, decreasing to 41% after its oxidation. Therefore, applied NO₂ ^– was a more effective inhibitor of CH₄ consumption than NH₄ ⁺. Temporary accumulation of NO₂ ^– during nitrification of added N was small (maximum: 1.9 mg NO₂ ^–-N kg^–1) and thus of minor importance with respect to the persistent inhibition after NH₄ ⁺ or urea application. CH₄ oxidation after NaNO₃ (40 mg N kg^–1) and NaCl addition did not differ to that of the untreated soil. The effect of organic manures on CH₄ oxidation depended on their C/N ratio: fresh sugar beet leaves enhanced mineralization, which caused an instantaneous 20% inhibition, whereas after wheat straw application available soil N was rapidly immobilized and no effect on CH₄ oxidation was found. The 28% increase in CH₄ oxidation after biowaste compost application was not related to its C/N ratio and was probably the result of an inoculation with methanotrophic bacteria. Only with high NH₄ ⁺ application rates (240 mg N kg^–1) could the persistent inhibitory effect partly be attributed to a pH decrease during nitrification. The exact reason for the observed persistent inhibition after a single, moderate NH₄ ⁺ or urea application is still unknown and merits further study. Received: 31 October 1997     

Induction of enhanced CH4 oxidation in soils: NH4 inhibition patterns

The influence of NH₄⁺ on microbial CH₄ oxidation is still poorly understood. Therefore, the influence of NH₄Cl and (NH₄)₂SO₄ on CH₄ oxidation was studied in soils at the different stages of the induction of enhanced methanotrophic activity. After a brief peak in the methanotrophic activity, a steady state was observed in which NH₄⁺ inhibited CH₄ oxidation at low CH₄ concentrations, and stimulated CH₄ oxidation at high concentrations. Chloride did not strongly inhibit CH₄ oxidation during this phase. During a second phase methanotrophic activity increased again. Ammonium no longer stimulated CH₄ oxidation, and Cl⁻ became an important source of uncompetitive inhibition. It was hypothesized that type I methanotrophs dominated during the first, soil-N-dependent phase while N₂-fixing type II methanotrophs dominated the second, soil-N-independent phase.     

Evaluation of the soil fauna impact on decomposition in a simulated coniferous forest soil

Summary Long-term experiments (ca. 2 years) were carried out in laboratory systems that simulated the complexity of a coniferous forest floor. The test materials were partially sterilized by freezing and thawing, and reinoculated with (1) microbes alone or (2) microbes with fauna. Removable microcosms containing birch litter, spruce litter, or humus were inserted into a humus substrate. Two experiments used organic matter only, and another included a layer of mineral soil below the humus. Both were incubated in climate chambers that simulated both summer and winter conditions. The evolution of CO₂ was measured at regular intervals. In order to determine the C content of the leachates, the macrocosms and the microcosms were watered periodically.Soil fauna significantly increased respiration in the litter, but not in the microcosms containing humus. In the later phases of decomposition the presence of fauna had a negative effect. In the total systems the fauna consistently increased the respiration rate. The loss of mass was greater in the presence of fauna, especially during the middle phases (5–11 months), but it was higher in the controls later.Throughout the whole incubation period the decomposition rate was strongly influenced by the composition of the animal community. The interpretation of the results is affected by the fact that the controls, to which no fauna had been added, contained dense populations of microbial feeders (nematodes, rotifers, and protozoans).     

Suppression of methane oxidation in aerobic soil by nitrogen fertilizers,nitrification inhibitors,and urease inhibitors

Concentrations of CH₄, a potent greenhouse gas, have been increasing in the atmosphere at the rate of 1% per year. The objective of these laboratory studies was to measure the effect of different forms of inorganic N and various N-transformation inhibitors on CH₄ oxidation in soil. NH ₄ ⁺ oxidation was also measured in the presence of the inhibitors to determine whether they had differential activity with respect to CH₄ and NH ₄ ⁺ oxidation. The addition of NH₄Cl at 25 g N g^-1 soil strongly inhibited (78–89%) CH₄ oxidation in the surface layer (0–15 cm) of a fine sandy loam and a sandy clay loam (native shortgrass prairie soils). The nitrification inhibitor nitrapyrin (5 g g^-1 soil) inhibited CH₄ oxidation as effectively as did NH₄Cl in the fine sandy loam (82–89%), but less effectively in the sandy clay loam (52–66%). Acetylene (5 mol mol^-1 in soil headspace) had a strong (76–100%) inhibitory effect on CH₄ consumption in both soils. The phosphoroamide (urease inhibitor) N-(n-butyl) thiophosphoric triamide (NBPT) showed strong inhibition of CH₄ consumption at 25 g g^-1 soil in the fine sandy loam (83%) in the sandy clay loam (60%), but NH ₄ ⁺ oxidation inhibition was weak in both soils (13–17%). The discovery that the urease inhibitor NBPT inhibits CH₄ oxidation was unexpected, and the mechanism involved is unknown.     

Methane oxidation in the soil surface layer of a flooded rice field and the effect of ammonium

Summary The CH₄ flux from intact soil cores of a flooded rice field in Italy was measured under aerobic and anaerobic incubation conditions. The difference between the anaerobic and aerobic CH₄ fluxes was apparently due to CH₄ oxidation in the oxic soil surface layer. This conclusion was supported by measurements of the vertical CH₄ profile in the upper 2-cm layer, and of the V _max of CH₄ oxidation in slurried samples of the soil surface layer. About 80% of the CH₄ was oxidized during its passage through the soil surface layer. CH₄ oxidation was apparently limited by the concentration of CH₄ and/or O₂ in the active surface layer. The addition of ammonium to the water layer on top of the soil core reversibly increased the aerobic CH₄ fluxes due to inhibition of CH₄ oxidation in the soil surface layer.     

Consequences of nitrogen fertilization on soil methane consumption in a productive temperate deciduous forest

To investigate the consequences of long-term N additions on soil CH₄ dynamics, we measured in situ CH₄ uptake rates, soil profiles and kinetics parameters during the growing season in a temperate deciduous forest in northwestern Pennsylvania (Allegheny College Bousson Environmental Forest). Measurements were made in control and adjacent plots amended with 100 kg N ha^–1 year^–1 for 8 years. We found that the in situ consumption rates were 0.19±0.02 (mean±SE) for the control and 0.12±0.01 mg CH₄–C m^–2 h^–1 for the N treatment, indicating that consumption had been reduced by 35% after 8 years of N amendments. Despite the large difference in rates of consumption, there were no differences in the CH₄ concentration profiles between the control and N-amended plots. Laboratory incubations of CH₄ consumption throughout the soil column (organic horizon and mineral soil depths) showed that rates were greatest in the organic horizon of both control and N-amended soils, although consumption was reduced by 42% in the N-amended plot. However, the rate in the organic horizon was only about 50% the rate measured in organic horizons at other temperate forests. The apparent K_m [K_m(app)] value in the organic horizon of the control plot was fourfold less than the K_m(app) value in the organic horizon of another temperate forest, but similar to the K_m(app) values in adjacent plots amended with N for a decade. Unlike results for other temperate forests, K_m(app) values at Bousson generally did not decrease with soil depth. These results indicate that N cycling strongly controls the CH₄-consuming community, and suggest that alterations of the N cycle due to N deposition or addition may alter rates and the location of CH₄ consumption by soils, even in soils with high N content and cycling rates.     

Effects of endogeic earthworms on soil processes and plant growth in coniferous forest soil

Summary The effects of the endogeic earthworm, Aporrectodea caliginosa tuberculata (Eisen) on decomposition processes in moist coniferous forest soil were studied in the laboratory. The pH preference of this species and its effects on microbial activity, N and P mineralization, and the growth of birch seedlings were determined in separate pot experiments. Homogenized humus from a spruce stand was shown to be too acid for A. c. tuberculata. After liming, the earthworms thrived in the humus and their biomass increased (at pH above 4.8). In later experiments in which the humus was limed, the earthworms positively influenced the biological activity in humus and also increased the rate of N mineralization. A. c. tuberculata increased the growth of birch seedlings, with increases observed in stems, leaves, and roots. Neither NH ₄ ⁺ -N fertilizer nor mechanical mixing with artificial worms affected seedling growth. No plant-growth-affecting compounds (e.g., hormone-like compounds) due to the earthworms were present in the humus. The shoot: root ratio in the birch seedlings was not affected by either the earthworms or the fertilizer. The experiments revealed the impact of earthworm activity on soil processes and plant growth.     

Microbial ethylene production and inhibition of methanotrophic activity in a deciduous forest soil

Production of C₂H₄, but not of CH₄, was observed in anoxically incubated soil samples (cambisol on loamy sand) from a deciduous forest. Ethylene production was prevented by autoclaving, indicating its microbial origin. Ethylene production gradually decreased from 4 to 12 cm soil depth and was not affected by moisture or addition of methionine, a possible precursor of C₂H₄. Oxidation of atmospheric CH₄ in soil samples was inhibited by C₂H₄. Ethylene concentrations of 3, 6 and 10 μl l⁻¹ decreased CH₄ uptake by 21, 63 and 98%, respectively. Methionine and methanethiol, a possible product of methionine degradation, also inhibited CH₄ oxidation. Under oxic conditions, C₂H₄ was consumed in the soil samples. Ethylene oxidation kinetics exhibited two apparent K_m values of 40 μl l⁻¹ and 12,600 μl l⁻¹ suggesting the presence of two different types of C₂H₄-oxidizing microorganisms. Methanotrophic bacteria were most probably not responsible for C₂H₄ oxidation, since the maximum of C₂H₄ oxidation activity was localized in soil layers (2-8 cm depth) above those (8-10 cm depth) of CH₄ oxidation activity. Our observations suggest that C₂H₄ production in the upper soil layers inhibits CH₄ oxidation, thus being one reason for the localization of methanotrophic activity in deeper soil layers.