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.     

Fluxes of methane and carbon dioxide from soil under forest, grazing land, irrigated rice and rainfed field crops in a watershed of Nepal

Field evolution of CH₄ and CO₂ from soils under four dominant land uses in the Mardi watershed, western Nepal, were monitored at 15-day intervals for 1 year using closed chamber techniques. The CH₄ oxidation rate (mean±SE, g CH₄ m^–2 h^–1) in the forest (22.8±6) was significantly higher than under grazing land (14±2) and an upland rainfed maize and millet system (Bari) (2.6±0.9). Irrigated rice fields (Khet) showed an oxidation rate of 6±0.8 g CH₄ m^–2 h^–1 in the dry season (December–May) but emitted a mean rate of 131 g CH₄ m^–2 h^–1 in the rainy season and autumn (June–October). The evolution of CO₂ ranged from 10 mg CO₂ m^–2 h^–1 in the Bari in January to 1,610 mg CO₂ m^–2 h^–1 in the forest in July. Higher evolution of CO₂ (mean±SE, mg CO₂ m^–2 h^–1) was observed in the Bari (399±39) and forest (357±36) compared to Khet (246±25) and grazing (206±20) lands. The annual emission of CO₂ evolution varied from 86.6 to 1,836 g CO₂ m^–2 year^–1. The activation energy for CH₄ and CO₂ varied between 16–283 and 80–117 kJ mol^–1, respectively. The estimated temperature coefficient for CO₂ emission varied from 2.5 to 5.0. Temperature explained 46–51% of the variation in CO₂ evolution, whereas it explained only 4–36% of the variation in CH₄ evolution.     

Agricultural factors affecting methane oxidation in arable soil

CH₄ oxidation activity in a sandy soil (Ardoyen) and agricultural practices affecting this oxidation were studied under laboratory conditions. CH₄ oxidation in the soil proved to be a biological process. The instantaneous rate of CH₄ consumption was in the order of 800 mol CH₄ kg^–1 day^–1 (13 mg CH₄ kg^–1 day^–1) provided the soil was treated with ca. 4.0 mmol CH₄ kg^–1 soil. Upon repeated supplies of a higher dose of CH₄, the oxidation was accelerated to a rate of at least 198 mg CH₄ kg^–1 day^–1. Addition of the plant-growth promoting rhizopseudomonad strains Pseudomonas aeruginosa 7NSK2 and Pseudomonas fluorescens ANP15 significantly decreased the CH₄ oxidation by 20 to 30% during a 5-day incubation. However, with further incubation this suppression was no longer detectable. Growing maize plants prevented the suppression of CH₄ oxidation. The numbers of methanotrophic bacteria and fungi increased significantly after the addition of CH₄, but there were no significant shifts in the population of total bacteria and fluorescent pseudomonads. Drying and rewetting of soil for at least 1 day significantly reduced the activity of the indigenous methanotrophs. Upon rewetting, their activity was regained after a lag phase of about 3 days. The herbicide dichlorophenoxy acetic acid (2,4-D) had a strong negative effect on CH₄ oxidation. The application of 5 ppm increased the time for CH₄ removal; at concentrations above 25 ppm 2,4-D CH₄–oxidizing activity was completely hampered. After 3 days of delay, only the treatments with below 25 ppm 2,4-D showed recovery of CH₄–oxidizing activity. This finding suggests that it can be important to include a CH₄–removal bioassay in ecotoxicology studies of the side effects of pesticides. Changes in the native soil pH also affected the CH₄–oxidizing capacity. Permanent inhibition occurred when the soil pH was altered by 2 pH units, and partial inhibition by 1 pH unit change. A rather narrow pH range (5.9–7.7) appeared to allow CH₄ oxidation. Soils pre-incubated with NH ₄ ⁺ had a lower CH₄–removal capacity. Moreover, the nitrification inhibitor 2-chloro-6-trichloromethyl pyridine (nitrapyrin) strongly inhibited CH₄ oxidation. Probably methanotrophs rather than nitrifying microorganisms are mainly responsible for CH₄ removal in the soil studied. It appears that the causal methanotrophs are remarkably sensitive to soil environmental disturbances.     

The inhibiting effect of nitrate fertilisation on methane uptake of a temperate forest soil is influenced by labile carbon

Upland soils are the most important terrestrial sink for the greenhouse gas CH₄. The oxidation of CH₄ is highly influenced by reactive N which is increasingly added to many ecosystems by atmospheric deposition and thereby also alters the labile C pool in the soils. The interacting effects of soil N availability and the labile C pool on CH₄ oxidation are not well understood. We conducted a laboratory experiment with soil columns consisting of homogenised topsoil material from a temperate broad-leaved forest to study the net CH₄ flux under the combined or isolated addition of NO ₃ ^? and glucose as a labile C source. Addition of NO ₃ ^? and glucose reduced the net CH₄ uptake of the soil by 86% and 83%, respectively. The combined addition of both agents led to a nearly complete inhibition of CH₄ uptake (reduction by 99.4%). Our study demonstrates a close link between the availability of C and N and the rate of CH₄ oxidation in temperate forest soils. Continued deposition of NO ₃ ^? has the potential to reduce the sink strength of temperate forest soils for CH₄.     

Trace gas emissions from soil of the central highlands of Mexico as affected by natural vegetation: a laboratory study

In the central highlands of Mexico, mesquite (Prosopis laevigata) and huisache (Acacia schaffneri), N₂-fixing trees or shrubs, dominate the vegetation and are currently used in a reforestation program to prevent erosion. We investigated how natural vegetation or cultivation of soil affected oxidation of CH₄, and production of N₂O. Soil was sampled under the canopy of mesquite (MES treatment) and huisache trees (HUI treatment), outside their canopy (OUT treatment) and from fields cultivated with maize (ARA treatment) at three different sites while production of CO₂, and dynamics of CH₄, N₂O and inorganic N (NH₄⁺, and NO₃^–) were monitored in an aerobic incubation. The production of CO₂ was 2.3 times higher and significantly greater in the OUT treatment, 3.0 times higher in the MES treatment and 4.0 times higher in the HUI treatment compared to the ARA treatment. There was no significant difference in oxidation of CH₄ between the treatments, which ranged from 0.019 g CH₄–C kg^–1 day^–1 for the HUI treatment to 0.033 CH₄–C kg^–1 day^–1 for the MES treatment. The production of N₂O was 30 g N₂O–N kg^–1 day^–1 in the MES treatment and >8 times higher compared to the other treatments. The average concentration of NO₃^– was 2 times higher and significantly greater in the MES treatment than in the HUI treatment, 3 times greater than in the OUT treatment and 10 times greater than in the ARA treatment. It was found that cultivation of soil decreased soil organic matter content, C and N mineralization, but not oxidation of CH₄ or production of N₂O.     

Labile carbon and methane uptake as affected by tillage intensity in a Mollisol

Methane (CH₄) oxidation potential of soils decreases with cultivation, but limited information is available regarding the restoration of that capacity with implementation of reduced tillage practices. A study was conducted to assess the impact of tillage intensity on CH₄ oxidation and several C-cycling indices including total and active microbial biomass C (t-MBC, a-MBC), mineralizable C (C_min) and N (N_min), and aggregate-protected C. Intact cores and disturbed soil samples (0–5 and 5–15 cm) were collected from a corn (Zea mays L.)–soybean (Glycine max L. Merr.) rotation under moldboard-plow (MP), chisel-plow (CP) and no-till (NT) for 8 years. An adjacent pasture (<25 years) and secondary growth forest (>60 years) soils were also sampled as references. At all sites, soil was a Kokomo silty clay loam (mesic Typic Argiaquolls). Significant tillage effects on t-MBC and protected C were found in the 0–5 cm depth. Protected C, a measure of C retained within macro-aggregates and defined as the difference in C_min (CO₂ evolved in a 56 days incubation) between intact and sieved (<2 mm) soil samples, amounted to 516, 162 and 121 mg C kg⁻¹ soil in the 0–5 cm layer of the forest, pasture and NT soils, respectively. Protected C was negligible in the CP and MP soils. Methane uptake rate (μg CH₄-C kg⁻¹ soil per day, under ambient CH₄) was higher in forest (2.70) than in pasture (1.22) and cropland (0.61) soils. No significant tillage effect on CH₄ oxidation rate was detected (MP: 0.82; CP: 0.41; NT: 0.61). These results underscore the slow recovery of the CH₄ uptake capacity of soils and suggest that, to have an impact, tillage reduction may need to be implemented for several decades.     

Controls of temporal and spatial variability of methane uptake in soils of a temperate deciduous forest with different abundance of European beech (Fagus sylvatica L.)

Aerated forest soils are a significant sink for atmospheric methane (CH₄). Soil properties, local climate and tree species can affect the soil CH₄ sink. A two-year field study was conducted in a deciduous mixed forest in the Hainich National Park in Germany to quantify the sink strength of this forest for atmospheric CH₄ and to determine the key factors that control the seasonal, annual and spatial variability of CH₄ uptake by soils in this forest. Net exchange of CH₄ was measured using closed chambers on 18 plots in three stands exhibiting different beech (Fagus sylvatica L.) abundance and which differed in soil acidity, soil texture, and organic layer thickness. The annual CH₄ uptake ranged from 2.0 to 3.4 kg CH₄-C ha⁻¹. The variation of CH₄ uptake over time could be explained to a large extent (R² = 0.71, P < 0.001) by changes in soil moisture in the upper 5 cm of the mineral soil. Differences of the annual CH₄ uptake between sites were primarily caused by the spatial variability of the soil clay content at a depth of 0-5 cm (R² = 0.5, P < 0.01). The CH₄ uptake during the main growing period (May-September) increased considerably with decreasing precipitation rate. Low CH₄ uptake activity during winter was further reduced by periods with soil frost and snow cover. There was no evidence of a significant effect of soil acidity, soil nutrient availability, thickness of the humus layer or abundance of beech on net-CH₄ uptake in soils in this deciduous forest. The results show that detailed information on the spatial distribution of the clay content in the upper mineral soil is necessary for a reliable larger scale estimate of the CH₄ sink strength in this mixed deciduous forest. The results suggest that climate change will result in increasing CH₄ uptake rates in this region because of the trend to drier summers and warmer winters.     

三峡库区2种土地利用方式下土壤盐基离子及碳氮含量对氮添加的响应

为探究三峡库区2种土地利用方式下土壤交换性盐基离子及土壤碳氮含量对氮添加的响应,以湖北省秭归县的林地和果园土壤为研究对象,进行室内土柱淋溶模拟试验,研究4种不同氮添加量(0,50,120,200 kg/(hm²·a))下,土壤中交换性Ca²⁺、Mg²⁺、Na⁺、K⁺以及NO₃^--N、DOC的变化。结果表明：随着氮添加量的增加,林地土壤中的交换性盐基离子淋失量显著增加(p<0.05),而果园土壤中的交换性盐基离子淋失量无显著变化,且林地土壤中交换性盐基离子淋失总量与各盐基离子淋失量均高于果园土壤;经N1、N2、N3处理后,与对照组(N0)相比,林地土壤中的交换性盐基离子淋失总量分别增加1.78%,4.45%,8.49%,且NO₃^--N淋失量分别增加89.21%,77.73%,157.25%,说明氮添加通过加剧土壤中NO₃^--N的淋失带走土壤中交...     

Quantification and potential availability of non-symbiotically fixed 15N in soil

Summary Non-symbiotic N₂ fixation was studied under laboratory conditions in two soils from Pakistan (Hafizabad silt loam and Khurrarianwala silt loam) and one from Illinois, USA (Drummer silty clay loam) incubated in a ¹⁵N-enriched atmosphere. N₂ fixation was greatest with the Drummer soil (18–122 g g^–1 soil, depending upon the soil treatment) and lowest with the Khurrarianwala soil (4–81 g g^–1 soil). Fixation was increased by the addition of glucose, a close correlation being observed between the amount of glucose added and the amount of N₂ fixed in the three soils (r = 0.96). Efficiency of N₂ fixation varied with soil type and treatment and was greatest in the presence of added inorganic P. Application of Mo apparently had a negative effect on the amount and efficiency of N₂ fixation in all the soils. The percentage of non-symbiotically fixed ¹⁵N in potentially mineralizable form (NH ₄ ⁺ -N released in soil after a 15-day incubation period under anaerobic conditions) was low (2%–18%, depending upon the soil treatment), although most of the fixed N (up to 90%) was recovered as forms hydrolysable with 6N HCl. Recovery in hydrolysable forms was much greater for the fixed N than for the native soil N, indicating that the former was more available for uptake by plants.     

Methane concentration and emission as affected by methane transport capacity of plants in freshwater marsh

To elucidate effect of the CH₄ transport capacity of plants on CH₄ production and CH₄ emission, we measured CH₄ emission and the CH₄ transport capacity of plants as well as CH₄ and dissolved organic carbon (DOC) concentrations in porewater and redox potential in the freshwater marsh vegetated with Carex lasiocarpa, Carex meyeriana and Deyeuxia angustifolia. Although only 31% of CH₄ emitted was released via Deyeuxia angustifolia into the atmosphere compared to 72–86% via Carex plants and the CH₄ transport capacity of per stem of Deyeuxia angustifolia was only 8.0 g CH₄ stem^–1 h^–1 being equal to half for Carex plants, the flux of CH₄ emission from the Deyeuxia angustifolia marsh was just lower by 17–28% than those from the Carex marshes as the standing water depth decreased significantly from 15–20 to 5 cm, indicating that despite the poor CH₄ transport capability of Deyeuxia angustifolia partly reduced CH₄ emission via plants, however CH₄ emission was not greatly reduced as expected. This is because although the poor gas transport capability of Deyeuxia angustifolia lowered CH₄ emission to some extent, however it also decreased the input of O₂ into the rhizosphere via plants; the latter not only reduced CH₄ oxidation in the rhizosphere and/or rhizome but also lowered redox potential in the vertical profile resulting in an increase in CH₄ production potential and CH₄ concentration especially at 5 cm depth, which in turn facilitated CH₄ emission through diffusion in the Deyeuxia angustifolia marsh. This study suggests that the sharp decrease in the CH₄ transport capacity of plants did not necessary result in an expected lowering of CH₄ emission in the freshwater marsh.     

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     

Effect of cultivation on microbial carbon and nitrogen in dry tropical forest soil

Summary Fifteen- and forty-year-old cropfields developed from a dry tropical forest were examined for soil organic C and total N and soil microbial C and N. The 15-year-old field had never been manured while the 40-year-old field had been fertilized with farmyard manure every year. The native forest soil was also examined. The results indicated that the native forest soil lost about 57% and 62% organic C and total N, respectively, in the 0–10 cm layer after 15 years of cultivation. The microbial C and N contents of the forest soil were greater than those of the cultivated soils. Application of farmyard manure increased the biomass-C and -N levels in the cultivated soil but the values were still markedly lower than in the forest soil. There was an appreciable seasonal variation in biomass C and N, the values being highest in summer and lowest in the rainy season. During an annual cycle, biomass-C contents varied from 180 to 727 g g^–1 and N from 20 to 80 g g^–1 dry soil, and both were linearly related. Microbial biomass C represented 1.6%–3.6% of total soil organic C and microbial biomass N represented 1.7% 1–4.4% of soil organic N.     

中国亚热带中部三峡库区不同土地利用方式下甲烷氧化潜力研究

To compare the CH4 oxidation potential among diferent land uses and seasons,and to observe its response to monsoon precipitation pattern and carbon and nitrogen parameters,a one-year study was conducted for diferent land uses (vegetable field,tilled and non-tilled orchard,upland crops and pine forest) in central subtropical China.Results showed significant diferences in CH4 oxidation potential among diferent land uses(ranging from 3.08 to 0.36 kg CH4 ha-1 year-1).Upland with corn-peanut-sweet potato rotation showed the highest CH4 emission,while pine forest showed the highest CH4 oxidation potential among all land uses.Non-tilled citrus orchard (0.72±0.08 kg CH4 ha-1 year-1)absorbed two times more CH4 than tilled citrus orchard(0.38±0.06kg CH4 ha-1 year-1).Irrespective of diferent vegetation,inorganic N fertilizer application significantly influenced CH4 fluxes across the sites (R2=0.86,P=0.002).Water-filled pore space,soil microbial biomass carbon,and dissolved nitrogen showed significant efects across diferent land uses (31% to 38% of variability)in one linear regression model.However,their cumulative interaction was significant for pine forest only,which might be attributed to undisturbed microbial communities legitimately responding to other variables,leading to net CH4 oxidation in the soil.These results suggested that i)natural soil condition tended to create win-win situation for CH4 oxidation,and agricultural activities could disrupt the oxidation potentials of the soils;and ii)specific management practices including but not limiting to efficient fertilizer application and utilization,water use efciency,and less soil disruption might be required to increase the CH4 uptake from the soil.     

Varying atmospheric methane concentrations affect soil methane oxidation rates and methanotroph populations in pasture,an adjacent pine forest,and a landfill

We describe experiments to better understand how CH₄ oxidation rates by different methanotroph communities respond to changing CH₄ concentrations. We used a novel system of automatically monitored chambers to investigate the response of CH₄ oxidation rates in a New Zealand pasture and adjacent pine forest soil exposed to varying atmospheric CH₄ concentrations.Type II methanotrophs that dominate CH₄ oxidation in the forest soil became progressively saturated as CH₄ concentrations rose from ambient (1.8 ppmv) to 570 ppmv, as shown by a decrease in uptake efficiency from 20% to 2% removal. By contrast, CH₄ oxidation in the pasture soil where Type I methanotrophs dominate increased in proportion to the increase in CH₄ inlet concentration, oxidising about 2% of the inlet CH₄ flux throughout. Modelling based on Michaelis-Menten kinetics revealed that low-affinity (Type I) methanotrophs were solely responsible for CH₄ oxidation in pasture soils, whereas high affinity (Type II) methanotrophs only contributed about 10% of the CH₄ oxidation in the forest soil. Increased aeration status using a soil–perlite (1:1) mixture doubled CH₄ oxidation rates at both ambient (1.8 ppmv) and 40 ppmv atmospheric CH₄. A similar volcanic soil previously exposed for 8 y to high CH₄ fluxes from a landfill had removal efficiencies consistently above 95% for atmospheric CH₄ concentrations up to 7500 ppmv when the CH₄ oxidation rate was7000 μg CH₄ kg⁻¹soil h⁻¹.     

Interactive effects of tree species and soil moisture on methane consumption

Methane consumption by temperate forest soils is a major sink for this important greenhouse gas, but little is known about how tree species influence CH₄ uptake by soils. Here, we show that six common tree species in Siberian boreal and temperate forests significantly affect potential CH₄ consumption in laboratory microcosms. Overall, soils under hardwood species (aspen and birch) consumed CH₄ at higher rates than soils under coniferous species and grassland. While NH₄⁺ addition often reduces CH₄ uptake, we found no effect of NH₄⁺ addition, possibly because of the relatively high ratio of CH₄-to-NH₄⁺ in our incubations. The effects of soil moisture strongly depended on plant species. An increase in soil moisture enhanced CH₄ consumption in soils under spruce but had the opposite effect under Scots pine and larch. Under other species, soil moisture did not affect CH₄ consumption. These results could be explained by specific responses of different groups of CH₄-oxidizing bacteria to elevated moisture.     

Effect of nitrogen deposition on CH4 uptake in forest soils in Hokkaido,Japan

Abstract

It has been well documented by short-term artificial experiments that the CH⁴ uptake is inhibited by N input, especially NH^{4 p+}-N input. To investigate the effect of the natural N input by throughfall and other factors on the CH⁴ uptake in forest soils, we measured the CH⁴ uptake rates for 6 months during the snow-free period of the year and N input by throughfall throughout the year at 10 sites in Hokkaido, Japan, from 1997 to 2002. Water filled pore space (WFPS) and pH values in the soils varied widely among the sites (38-93% and 3.9-6.2, respectively). The rates of NH^{4 p+}-N and NH^{3 p-}-N inputs ranged from 1.3 to 6.9 kg N ha^p-1 year^p-1 and from 0.8 to 2.9 kg N ha^p-1 year^p-1, respectively. The NH^{4 p+}-N input was generally higher than the NH^{3 p-}-N input. Total N input by throughfall amounted to 2.3-9.4 kg N ha^p-1 year^p-1. The highest CH⁴ uptake rate occurred within the period from July to September (41-215 μg CH⁴ m^p-2 h^p-1) each year at most sites. CH⁴ uptake rate was relatively low (~50 μg CH⁴ M-2 h^p-1) at northern sites, while a high CH⁴ uptake rate was observed throughout the year 100 (? CH⁴ m^p-2 h^p-1) at southern sites. The mean CH⁴ uptake rates were significantly different among the sites. Cumulative CH⁴ uptake ranged from 1.4 to 6.6 kg CH⁴ ha^p-1 [184 d]^p-1 with a mean values of 3.22 ± 1.36 kg CH⁴ ha^p-1 [184 d]^p-1. Cumulative CH⁴ uptake increased with increasing temperature and decreased with an increase in precipitation (Rain), NH^{4 p+}-N input (TF^NH4) WFPS, soil total C (TC), and total N (TN). There was a quadratic relationship between the CH⁴ uptake and NH^{3 p-}-N input (TF^NO3), soil pH, and C / N ratio in soil. A regression equation was obtained as follows to predict the CH⁴ uptake in forest soils: Cumulative CH⁴ uptake = 0.47 / Rain + 0.38 / TF^NH4 + 0.34 / TC - 0.30 / TF^N03 (R ^p2 = 0.74, p = 0.0001). This equation indicates that atmospheric N input into forest soils is one of the main factors that control cumulative CH⁴ uptake with precipitation, total carbon content in soil in Hokkaido, Japan.     

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.     

Distinct effect of nitrogen fertilisation and soil depth on nitrous oxide emissions and nitrifiers and denitrifiers abundance

The nitrous oxide and molecular N emissions from 5-cm length subsamples taken from 20-cm length sample corers containing eutric Cambisol soil fertilised either with urea, ammonium or nitrate for 1 year have been examined using gas chromatography. At the beginning of the incubation, the same N rate (260 kg N/ha) was added to the soil and kept constant during the experiment. The total abundance of the soil Bacteria and Archaea and that of nitrifiers and denitrifiers was estimated by quantitative PCR of the corresponding biotic variables 16S rRNA, amoA and napA, narG, nirK, nirS, norB, nosZI and nosZII genes. The abiotic variables dissolved oxygen, pH, exchangeable NH₄⁺-N and NO₃^?-N contents and total C and total N were also analysed. None of the three fertilisers affected the total abundance of Bacteria and Archaea and nitrification was the main driver of nitrous oxide production in the 0- to 5-cm and 5- to 10-cm soil layers while denitrification was in the 10- to 15-cm and 15- to 20-cm soil horizons. Parallel to the reduction in the content of dissolved oxygen along the soil profile, there was a decrease in the total and relative abundance of the bacterial and archaeal amoA gene and an increase in the abundances of the denitrification genes, mainly in the 10- to 15-cm and 15- to 20-cm soil layers. A non-metric multidimensional scaling plot comparing the biotic and abiotic variables examined in each of the four 5-cm soil subsamples and the whole 20-cm sample showed a disparate effect of N fertilisation on N gas emissions and abundance of nitrifiers and denitrifiers bacterial and archaeal communities.     

Effect of summer throughfall exclusion, summer drought, and winter snow cover on methane fluxes in a temperate forest soil

Soil moisture strongly controls the uptake of atmospheric methane by limiting the diffusion of methane into the soil, resulting in a negative correlation between soil moisture and methane uptake rates under most non-drought conditions. However, little is known about the effect of water stress on methane uptake in temperate forests during severe droughts. We simulated extreme summer droughts by exclusion of 168 mm (2001) and 344 mm (2002) throughfall using three translucent roofs in a mixed deciduous forest at the Harvard Forest, Massachusetts, USA. The treatment significantly increased CH₄ uptake during the first weeks of throughfall exclusion in 2001 and during most of the 2002 treatment period. Low summertime CH₄ uptake rates were found only briefly in both control and exclusion plots during a natural late summer drought, when water contents below 0.15 g cm⁻³ may have caused water stress of methanotrophs in the A horizon. Because these soils are well drained, the exclusion treatment had little effect on A horizon water content between wetting events, and the effect of water stress was smaller and more brief than was the overall treatment effect on methane diffusion. Methane consumption rates were highest in the A horizon and showed a parabolic relationship between gravimetric water content and CH₄ consumption, with maximum rate at 0.23 g H₂O g⁻¹ soil. On average, about 74% of atmospheric CH₄ was consumed in the top 4-5 cm of the mineral soil. By contrast, little or no CH₄ consumption occurred in the O horizon. Snow cover significantly reduced the uptake rate from December to March. Removal of snow enhanced CH₄ uptake by about 700-1000%, resulting in uptake rates similar to those measured during the growing season. Soil temperatures had little effect on CH₄ uptake as long as the mineral soil was not frozen, indicating strong substrate limitation of methanotrophs throughout the year. Our results suggest that the extension of snow periods may affect the annual rate of CH₄ oxidation and that summer droughts may increase the soil CH₄ sink of temperate forest soils.     

Nitrogen addition impacts on the emissions of greenhouse gases depending on the forest type: a case study in Changbai Mountain,Northeast China

Purpose

Anthropogenic-induced greenhouse gas (GHG) emission rates derived from the soil are influenced by long-term nitrogen (N) deposition and N fertilization. However, our understanding of the interplay between increased N load and GHG emissions among soil aggregates is incomplete.

Materials and methods

Here, we conducted an incubation experiment to explore the effects of soil aggregate size and N addition on GHG emissions. The soil aggregate samples (0–10 cm) were collected from two 6-year N addition experiment sites with different vegetation types (mixed Korean pine forest vs. broad-leaved forest) in Northeast China. Carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄) production were quantified from the soil samples in the laboratory using gas chromatography with 24-h intervals during the incubation (at 20 °C for 168 h with 80 % field water capacity).

Results and discussion

The results showed that the GHG emission/uptake rates were significantly higher in the micro-aggregates than in the macro-aggregates due to the higher concentration of soil bio-chemical properties (DOC, MBC, NO₃ ^?, NH₄ ⁺, SOC and TN) in smaller aggregates. For the N addition treatments, the emission/uptake rates of GHG decreased after N addition across aggregate sizes especially in mixed Korean pine forest where CO₂ emission was decreased about 30 %. Similar patterns in GHG emission/uptake rates expressed by per soil organic matter basis were observed in response to N addition treatments, indicating that N addition might decrease the decomposability of SOM in mixed Korean pine forest. The global warming potential (GWP) which was mainly contributed by CO₂ emission (>98 %) decreased in mixed Korean pine forest after N addition but no changes in broad-leaved forest.

Conclusions

These findings suggest that soil aggregate size is an important factor controlling GHG emissions through mediating the content of substrate resources in temperate forest ecosystems. The inhibitory effect of N addition on the GHG emission/uptake rates depends on the forest type.