Influence of forest disturbance on CO2, CH4 and N2O fluxes from larch forest soil in the permafrost taiga region of eastern Siberia

Abstract

To evaluate the effect of increasing forest disturbances on greenhouse gas budgets in a taiga forest in eastern Siberia, CO₂, CH₄ and N₂O fluxes from the soils were measured during the growing season in intact, burnt and clear-felled larch forests (4–5 years after the disturbance). Soil temperature and moisture were higher at the two disturbed sites than at the forest site. A 64–72% decrease in the Q ₁₀ value of soil CO₂ flux from the disturbed sites compared with the forest site (5.92) suggested a reduction in root respiration and a dominance of organic matter decomposition at the disturbed sites. However, the cumulative CO₂ emissions (May–August) were not significantly different among the sites (2.81–2.90 Mg C ha^?1 per 3 months). This might be because decreased larch root respiration was compensated for by increased organic matter decomposition resulting from an increase in the temperature and root respiration of invading vegetation at the disturbed sites. The CH₄ uptake (kg C ha^?1 per 4 months [May–September]) at the burnt site was significantly higher (–0.15) than the uptake at the forest (–0.045) and clear-felled sites (0.0027). Although there were no significant differences among the sites, N₂O emission (kg N ha^?1 per 4 months) was slightly lower at the burnt site (0.013) and higher at the clear-felled site (0.068) than at the forest site (0.038). This different influence of burning and tree felling on CH₄ and N₂O fluxes might result from changes in the physical and chemical properties of the soil with respect to forest fire.     

Comparison of N2O and CO2 concentrations and fluxes in the soil profile between a Gray Lowland soil and an Andosol

Abstract

We measured nitrous oxide (N₂O) and carbon dioxide (CO₂) fluxes from the soil surface and in the soil through to a depth of 0.3?m, and their concentration profiles through to a depth of 0.6?m in both a Gray Lowland soil with macropores and cracks and an Andosol with undeveloped soil structure in central Hokkaido, Japan. The objective of the present study was to elucidate any differences in N₂O production and flux in the soil profile between these two soil types. In the Gray Lowland soil, the N₂O concentration above 0.4?m increased with an increase in soil depth. In the Andosol, there were no distinctive N₂O concentration gradients in the topsoil when the N₂O flux did not increase. However, the N₂O concentration at a depth of 0.1?m significantly increased and this concentration was higher than the concentration below 0.2?m when the N₂O flux greatly increased. Thus, the N₂O concentration profiles were different between these two soils. The contribution ratios of the N₂O produced in the top soil (0–0.3?m depth) to the total N₂O emitted from the soil to the atmosphere in the Gray Lowland soil and the Andosol were 0.86 and 1.00, respectively, indicating that the N₂O emitted from the soil to the atmosphere was mainly produced in the top soil. However, the contribution ratio of the subsoil to the N₂O emitted from the Gray Lowland soil was higher than that of the Andosol. There was a significant positive correlation between the N₂O flux through to a 0.3?m depth and the flux from the soil to the atmosphere in the Gray Lowland soil only. These results suggest that N₂O production in the subsoil of the Gray Lowland soil could have been activated by NO₃ ^? leaching through macropores and cracks, and subsequently the N₂O produced in the subsoil could have been rapidly emitted to the atmosphere through the macropores and cracks.     

Repeated drying–rewetting cycles and their effects on the emission of CO2, N2O,NO, and CH4 in a forest soil

Prolonged summer droughts due to climate change are expected for this century, but little is known about the effects of drying and wetting on biogenic trace‐gas fluxes of forest soils. Here, the response of CO₂, N₂O, NO, and CH₄ fluxes from temperate forest soils towards drying–wetting events has been investigated, using undisturbed soil columns from a Norway spruce forest in the “Fichtelgebirge”, Germany. Two different types of soil columns have been used for this study to quantify the contribution of organic and mineral horizons to the total fluxes: (1) organic horizons (O) and (2) organic and mineral soil horizons (O+M). Three drying–wetting treatments with different rewetting intensities (8, 20, and 50 mm of irrigation d^–1) have been compared to a constantly moist control to estimate the influence of rainfall intensity under identical drying conditions and constant temperature (+15°C). Drought significantly reduced CO₂, N₂O, and NO fluxes in most cycles. Following rewetting, CO₂ fluxes quickly recovered back to control level in the O columns but remained significantly reduced in the O+M columns with total CO₂ fluxes from the drying–wetting treatment ranging approx. 80% of control fluxes. Fluxes of N₂O and NO remained significantly reduced in both O and O+M columns even after rewetting, with cumulative fluxes from drying–wetting treatments ranging between 20% and 90% of the control fluxes, depending on gas and cycle. Fluxes of CH₄ were small in all treatments and seem to play no significant role in this soil. No evidence for the release of additional gas fluxes due to drying–wetting was found. The intensity of rewetting had no significant effect on the CO₂, N₂O, NO, and CH₄ fluxes, suggesting that the length of the drought period is more important for the emission of these gases. We can therefore not confirm earlier findings that fluxes of CO₂, N₂O, and NO during wetting of dry soil exceed the fluxes of constantly moist soil.     

N2O and CH4 fluxes from a volcanic grassland soil in Nasu,Japan: Comparison between manure plus fertilizer plot and fertilizer-only plot

Abstract

We examined the effects of manure + fertilizer application and fertilizer-only application on nitrous oxide (N₂O) and methane (CH₄) fluxes from a volcanic grassland soil in Nasu, Japan. In the manure + fertilizer applied plot (manure plot), the sum of N mineralized from the manure and N applied as ammonium sulfate was adjusted to 210 kg N ha^?1 year^?1. In the fertilizer-only applied plot (fertilizer plot), 210 kg N ha^?1 year^?1 was applied as ammonium sulfate. The manure was applied to the manure plot in November and the fertilizer was applied to both plots in March, May, July and September. From November 2004 to November 2006, we regularly measured N₂O and CH₄ fluxes using closed chambers. Annual N₂O emissions from the manure and fertilizer plots ranged from 7.0 to 11.0 and from 4.7 to 9.1 kg N ha^?1, respectively. Annual N₂O emissions were greater from the manure plot than from the fertilizer plot (P < 0.05). This difference could be attributed to N₂O emissions following manure application. N₂O fluxes were correlated with soil temperature (R = 0.70, P < 0.001), NH⁺ ₄ concentration in the soil (R = 0.67, P < 0.001), soil pH (R = –0.46, P < 0.001) and NO^? ₃ concentration in the soil (R = 0.40, P < 0.001). When included in the multiple regression model (R = 0.72, P < 0.001), however, the following variables were significant: NH⁺ ₄ concentration in the soil (β = 0.52, P < 0.001), soil temperature (β = 0.36, P < 0.001) and soil moisture content (β = 0.26, P < 0.001). Annual CH₄ emissions from the manure and fertilizer plots ranged from –0.74 to –0.16 and from –0.84 to –0.52 kg C ha^?1, respectively. No significant difference was observed in annual CH₄ emissions between the plots. During the third grass-growing period from July to September, however, cumulative CH₄ emissions were greater from the manure plot than from the fertilizer plot (P < 0.05). CH₄ fluxes were correlated with NH⁺ ₄ concentration in the soil (R = 0.21, P < 0.05) and soil moisture content (R = 0.20, P < 0.05). When included in the multiple regression model (R = 0.29, P < 0.05), both NH⁺ ₄ concentration in the soil (β = 0.20, P < 0.05) and soil moisture content (β = 0.20, P < 0.05) were significant.     

Groundwater level controls CO2, N2O and CH4 fluxes of three different hydromorphic soil types of a temperate forest ecosystem

Hydromorphic soils should exhibit higher climate change feedback potentials than well aerated soils since soil organic matter (SOM) losses in them are predicted to be much larger than those of well aerated soils. To evaluate a combined feedback relationship between groundwater level (GWL) and total greenhouse gas (GHG) emission, a greenhouse microcosm experiment was performed by exposing three hydromorphic forest soil types that differed in carbon content to three water levels (?40, ?20 and ?5 cm) while plants were excluded. Net GHG fluxes were measured continuously. GHG concentrations plus oxygen were measured in soil air and soil water at different depths. In this study, soil type hardly affected GHG emissions but GWL did. CO₂ emissions peaked at GWL of ?40 cm and declined on average to 65 and 33% during GWL at ?20 and ?5 cm, respectively. CH₄ emissions showed the opposite pattern having the highest emission rates at GWL of ?5 cm and compared to that on average only ?3 and ?8% during GWL at ?20 and ?40 cm, respectively. The highest mean N₂O emissions were detected at the intermediate GWL of ?20 cm, whereas it is reduced on average to 18% for GWL at ?40 cm and at ?5 cm. The highest greenhouse gas emissions (in CO₂ equivalents) were calculated for GWL at ?20 cm. During GWL at ?40 cm, CO₂ equivalent fluxes were only insignificantly lower. CO₂ equivalent fluxes reduced explicitly in mean to 35% with GWL at ?5 cm. The outcome emphasizes that anaerobic SOM decomposition apparently produces a lower warming potential than aerobic SOM decomposition. Undoubtedly, hydromorphic soils have to be considered for climate–carbon feedback scenarios.     

Emissions of trace gases (CO2, CO,CH4, and N2O) resulting from rice straw burning

Emissions of trace gases (CO₂, CO, CH₄, N₂O) resulting from rice straw burning were measured by using the open chamber method. The carbon contained in rice straw was mainly released to the atmosphere as CO₂. The percentage of CO₂-C emitted in total C in rice straw was in the range of 57–81%, followed by CO-C (5–9%). The percentages of CH₄-C and N₂O-N in total C and N in rice straw were in the range of 0.43–0.90 and 1.16–1.50%, respectively. In the case of the rice straw which had been left in the field for a period of one month after harvest, emission of imperfect combustible gases such as CO and CH₄ during burning increased slightly, while that of perfect combustible gas, CO₂, was reduced. The amount of CH₄ emission from rice straw burning was comparable to that from paddy fields.     

硅胶管气样原位采集技术研究土壤N_2O浓度及通量变化

箱法被广泛用于监测土壤N_2O排放通量,但在原位采集高浓度土壤N_2O、全天候监测N_2O通量变化、动态研究土壤剖面N_2O的行为等方面存在弊端.本研究通过室内模拟硅胶管对N_2O的通透性,探索硅胶管用于原位采集土壤气样的理论可行性.田间试验设施用铵态氮肥(NH_4~+)、施用硝态氮肥(NO_3~-)及施用硝态氮肥加葡萄糖(NO_3~-+C)等3个处理,同时安置硅胶管和采样箱,验证硅胶管法在原位采集高浓度土壤N_2O气样、监测土壤N_2O浓度以及排放通量的实际效果,并与箱法进行比较.结果表明,硅胶管内外的N_2O气体经2.9 h达到95%的平衡,完伞能满足大田采样要求;用硅胶管法原位采集高浓度土壤N_2O气样的效果显著优于箱法采样.其浓度变化表现出明显的时间规律,浓度梯度法计算的N_2O排放通量与箱法测定结果呈显著正相关,但数值偏低;偏低的程度取决于采样位置和土壤中N_2O产生位置的匹配程度.建议采用埋于土壤表层的硅胶管计算地面N_2O排放通量,或在不同土层埋人硅胶管研究土壤剖面N_2O行为的时空变异.     

Relationships between ammonia oxidizers and N2O and CH4 fluxes in agricultural fields with different soil types

Nitrous oxide (N₂O) is a greenhouse gas that contributes to the destruction of stratospheric ozone, and agricultural soil is an important source of N₂O. Aerobic soils are sinks for atmospheric methane (CH₄), a greenhouse gas. Ammonia monooxygenase (AMO) can oxidize CH₄, but CH₄ is mostly oxidized by methane monooxygenase (MMO), and CH₄ oxidation by AMO is generally negligible in the soil. We monitored the N₂O and CH₄ fluxes after urea application in fields containing different soils using an automated sampling system to determine the effects of environmental and microbial factors on the N₂O and CH₄ fluxes. The soil types were Low-humic Andosol (Gleyic Haplic Andosol), yellow soil (Gleyic Haplic Alisol) and gray lowland soil (Entric Fluvisol). Cumulative N₂O emissions from the yellow soil were higher than those from other soil types, although the difference was not significant. The CH₄ uptake level by Andosol was one order of magnitude higher than that by other soils. There were significant relationships between the ammonia oxidation potential, AOB and AOA amoA copy numbers, and the CH₄ uptake. In contrast, the gene copy numbers of methane-oxidizing bacteria (MOB) pmoA were below the detection limit. Our results suggested that the AMOs of AOB and AOA may have more important roles than those previously considered during CH₄ oxidation in agricultural soils treated with N fertilizers.     

CO2, CH4 and N2O fluxes of upland black spruce (Picea mariana) forest soils after forest fires of different intensity in interior Alaska

Abstract

Forest fires can change the greenhouse gase (GHG) flux of borea forest soils. We measured carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) fluxes with different burn histories in black spruce (Picea mariana) stands in interior Alaska. The control forest (CF) burned in 1920; partially burned (PB) in 1999; and severely burned (SB1 and SB2) in 2004. The thickness of the organic layer was 22 ± 6 cm at CF, 28 ± 10 cm at PB, 12 ± 6 cm at SB1 and 4 ± 2 cm at SB2. The mean soil temperature during CO₂ flux measurement was 8.9 ± 3.1, 6.4 ± 2.1, 5.9 ± 3.4 and 5.0 ± 2.4°C at SB2, SB1, PB and CF, respectively, and differed significantly among the sites (P < 0.01). The mean CO₂ flux was highest at PB (128 ± 85 mg CO₂-C m^?2 h^?1) and lowest at SB1 (47 ± 19 mg CO₂-C m^?2 h^?1) (P < 0.01), and within each site it was positively correlated with soil temperature (P < 0.01). The CO₂ flux at SB2 was lower than that at CF when the soil temperature was high. We attributed the low CO₂ flux at SB1 and SB2 to low root respiration and organic matter decomposition rates due to the 2004 fire. The CH₄ uptake rate was highest at SB1 [–91 ± 21 μg CH₄-C m^?2 h^?1] (P < 0.01) and positively correlated with soil temperature (P < 0.01) but not soil moisture. The CH₄ uptake rate increased with increasing soil temperature because methanotroph activity increased. The N₂O flux was highest [3.6 ± 4.7 μg N₂O-N m^?2 h^?1] at PB (P < 0.01). Our findings suggest that the soil temperature and moisture are important factors of GHG dynamics in forest soils with different fire history.     

Aeration effects on CO2, N2O,and CH4 emission and leachate composition of a forest soil

The availability of O₂ is one of the most important factors controlling the chemical and biological reactions in soils. In this study, the effects of different aeration conditions on the dynamics of the emission of trace gases (CO₂, N₂O, CH₄) and the leachate composition (NO₃^‐, DOC, Mn, Fe) were determined. The experiment was conducted with naturally structured soil columns (silty clay, Vertisol) from a well aerated forest site. The soil monoliths were incubated in a microcosm system at different O₂ concentrations (0, 0.001, 0.005, 0.01, 0.05, and 0.205 m³ m^‐3 in the air flow through the headspace of the microcosms) for 85 days. Reduced O₂ availability resulted in a decreased CO₂ release but in increased N₂O emission rates. The greatest cumulative N₂O emissions (= 1.6 g N₂O‐N m^‐2) were observed at intermediate O₂ concentrations (0.005 and 0.01 m³ m^‐3) when both nitrification and denitrification occurred simultaneously in the soil. Cumulative N₂O emissions were smallest (= 0.05 g N₂O‐N m^‐2) for the aeration with ambient air (O₂ concentration: 0.205 m³ m^‐3), although nitrate availability was greatest in this treatment. The emission of CH₄ and leaching of Mn and Fe were restricted to the soil columns incubated under completely anoxic conditions. The sequence of the reduction processes under completely anoxic conditions complied with the thermodynamic theory: soil nitrate was reduced first, followed by the reduction of Mn(IV) and Fe(III) and finally CO₂ was reduced to CH₄. The re‐aeration of the soil columns after 85 days of anoxic incubation terminated the production of CH₄ and dissolved Fe and Mn in the soil but strongly increased the emission rates of CO₂ and N₂O and the leaching of NO₃^‐ probably because of the accumulation of DOC and NH₄⁺ during the previous anoxic period.     

CFD模拟气调库快速降氧过程O_2和CO_2浓度变化规律

O2和CO2浓度对果蔬的贮藏品质有着极大的影响,获得其在气调库内的变化和分布规律可以为气调库优化设计提供理论依据。该文以西安某苹果气调库为研究对象,采用k-ε紊流模型建立了气调库内气体流动、传热与传质的三维数学求解模型,并通过编写UDF程序获得苹果呼吸强度和冷风机送风口O2、CO2质量分数随库内气体组分浓度变化实时数据。经过对该气调库的快速降氧过程数值模拟获得库内O2和CO2浓度随时间变化的规律,并与试验数据呈现较好的一致性,相对偏差平均值为0.027。结果表明库内气体区O2浓度随时间呈指数衰减。该文的研究对象经过4.1 h,气体区O2浓度下降速度小于货物区,此时提高制氮机制氮体积分数会缩短降氧时间。气体区和货物区CO2浓度变化规律相似,升高速度逐渐变小。库内O2和CO2浓度分布在气体区比较均匀,在货物区则存在一定的梯度,货物区中心位置不利于果蔬的贮藏。该文研究对于获取实际气调库降氧时间及选择合理的制氮机,改进气调工艺具有重要参考价值。     

Emissions of CH4, CO2, and N2O from soil at a cattle overwintering area as affected by available C and N

Relationships between CH₄, CO₂, and N₂O emissions were studied in soil that had been freshly amended with large deposits of cattle wastes. Dynamics of CH₄, CO₂, and N₂O emissions were investigated with flux chambers from early April to late June 2011, during the 3 months following cattle overwintering at the site. This 81-day field study was supplemented with soil analyses of available C and N content and measurement of denitrification activity. In a more detailed field investigation, the daily time course of emissions was determined. The field research was complemented with a laboratory experiment that focused on the short-term time course of N₂O and CH₄ production in artificially created anoxic soil microsites. The following hypotheses were tested: (i) a large input of C (and N and other nutrients) in cattle manure creates conditions suitable for methanogenesis, and therefore overwintering areas can produce large amounts of CH₄; (ii) N₂O is produced and emitted until the level of mineral N decreases, while the level of CH₄ production is low; and (iii) production of CH₄ is greater when N immobilization decreases the level of NO₃⁻ in soil. N₂O emissions were relatively large during the first 3 weeks, then peaked (at ca. 4000 μg N₂ON m⁻² h⁻¹) and soon decreased to almost zero; the changes were related to the mineral and soluble organic N content in soil. CH₄ fluxes were large, though variable, in the first 2 months (600–3000 μg CH₄C m⁻² h⁻¹) and were independent of C and N availability. Although time courses differed for CH₄ and N₂O, a negative relationship between N₂O and CH₄ emissions was not detected. Contrary to CH₄ and N₂O fluxes, CO₂ emissions progressively increased to ca. 300 mg CO₂C m⁻² h⁻¹ at the end of the field study and were closely related to air and soil temperatures. Diurnal measurements revealed significant correlations between temperature and emissions of CH₄, N₂O, and CO₂. Addition of C to soil during anaerobic incubation increased the production and consumption of N₂O and supported the emission of CH₄. The results suggest that rapid denitrification significantly contributes to the exhaustion of oxidizing agents and helps create microsites supporting methanogenesis in otherwise N₂O-producing upland soil. The results also indicate that accurate estimate of gas fluxes in animal-impacted grassland areas requires assessment of both diurnal and long-term changes in CH₄, CO₂, and N₂O emissions.     

Short‐term N2O,CO2, NH3 fluxes,and N/C transfers in a Danish grass‐clover pasture after simulated urine deposition in autumn

Urine patches are significant hot‐spots of C and N transformations. To investigate the effects of urine composition on C and N turnover and gaseous emissions from a Danish pasture soil, a field plot study was carried out in September 2001. Cattle urine was amended with two levels of ¹³C‐ and ¹⁵N‐labeled urea, corresponding to 5.58 and 9.54 g urea‐N l^–1, to reflect two levels of protein intake. Urine was then added to a sandy‐loam pasture soil equivalent to a rate of 23.3 or 39.8 g urea‐N m^–2. Pools and isotopic labeling of nitrous oxide (N₂O) and CO₂ emissions, extractable urea, ammonium (NH₄⁺), and nitrate (NO₃^–), and plant uptake were monitored during a 14 d period, while ammonia (NH₃) losses were estimated in separate plots amended with unlabeled urine. Ammonia volatilization was estimated to account for 14% and 12% of the urea‐N applied in the low (UL) and high (UH) urea treatment, respectively. The recovery of urea‐derived N as NH₄⁺ increased during the first several days, but isotopic dilution was significant, possibly as a result of stress‐induced microbial metabolism. After a 2 d lag phase, nitrification proceeded at similar rates in UL and UH despite a significant difference in NH₄⁺ availability. Nitrous oxide fluxes were low, but generally increased during the 14 d period, as did the proportion derived from urea‐N. On day 14, the contribution from urea was 23% (UL) and 13% (UH treatment), respectively. Cumulative total losses of N₂O during the 14 d period corresponded to 0.021% (UL) and 0.015% (UH) of applied urea‐N. Nitrification was probably the source of N₂O. Emission of urea‐derived C as CO₂ was only detectable within the first 24 h. Urea‐derived C and N in above‐ground plant material was only significant at the first sampling, indicating that uptake of urine‐C and N via the leaves was small. Urine composition did not influence the potential for N₂O emissions from urine patches under the experimental conditions, but the importance of site conditions and season should be investigated further.     

Effects of nitrogen and sulfur deposition on CH4 and N2O fluxes in high-altitude peatland soil under different water tables in the Tibetan Plateau

Abstract

The effects of nitrogen (N) and sulfur (S) deposition on methane (CH₄) and nitrous oxide (N₂O) emissions under low (10 cm below soil surface) and high (at soil surface) water tables were investigated in the laboratory. Undisturbed soil columns from the alpine peatland of the Tibetan Plateau were analyzed. CH₄ emission was higher and N₂O emission was lower at the high water table than those at the low water table regardless of nutrient application. Addition of N (NH₄NO₃ (ammonium nitrate), 5 g N m^?2) decreased CH₄ emission up to 57% and 50% at low and high water tables, respectively, but correspondingly increased N₂O emission by 2.5 and 10.4 times. Addition of S (Na₂SO₄ (sodium sulfate), 2.5 g S m^?2) decreased CH₄ and N₂O emission by 64% and 79% at the low water table, respectively, but had a slightly positive effect at the high water table. These results indicated that the responses of CH₄ and N₂O emissions to the S deposition depend on the water table condition in the high-altitude peatland.     

Effects of mixing biochar on soil N2O,CO2, and CH4 emissions after prescribed fire in alpine meadows of Wugong Mountain,China

Journal of Soils and Sediments - Prescribed fires or wildfires are common in natural ecosystems. Biochar input during fires can impact soil greenhouse gas (GHG) emissions, including methane (CH4),...     

A new sampling technique to monitor concentrations of CH4, N2O and CO2 in air at well‐defined depths in soils with varied water potential

A new sampling technique for measuring the concentrations of trace gases (CH₄, CO₂ and N₂O) in the soil atmosphere from well‐defined depths is described. Probes are constructed from silicone tubing closed with silicone septa on both ends, thereby dividing an inner air space from the outer soil atmosphere without a direct contact. The gas exchanges between the inner and outer atmosphere only by diffusion through the walls of the silicone tube. Tests revealed that the gases N₂O, CO₂ and CH₄ in the enclosed space reached 95% equilibrium with the surrounding atmosphere at 20°C within 7 h or faster. The probe measurements are reproducible: the standard deviation of samples taken from 26 probes stored in the laboratory atmosphere equalled that of a standard gas. The probes can easily be constructed and installed at specified depths in the soil. The method has the following advantages compared with other methods that use spaces with holes in them for gas exchange: (i) the silicone probe enables trace gases to be sampled in wet soils, including ones that are waterlogged or temporarily saturated; (ii) the sampling itself does not create low pressure and hence does not create mass flow in the soil matrix from undefined depths; and (iii) the probe can be made to take samples of gas of any required size. The silicone probes did not show ageing effects during 18 months of use in the field in a mineral soil under grass. The probes yielded comparable results: three probes inserted at 5 cm depth in a uniformly treated 100‐m² plot provided nearly identical average trace gas concentrations within the measurement period.     

Variability of CO2 and N2O emissions during freeze‐thaw cycles: results of model experiments on undisturbed forest‐soil cores

The amounts of N₂O released in periods of alternate freezing and thawing depend on site and freezing conditions, and contribute considerably to the annual N₂O emissions. However, quantitative information on the N₂O emission level of forest soils in freeze‐thaw cycles is scarce, especially with regard to the direct and indirect effect of tree species and the duration of freezing. Our objectives were (i) to quantify the CO₂ and N₂O emissions of three soils under beech which differed in their texture, C and N contents, and humus types in freeze‐thaw cycles, and (ii) to study the effects of the tree species (beech (Fagus sylvatica L.) and spruce (Picea abies (L.) Karst.)) for silty soils from two adjacent sites and the duration of freezing (three and eleven days) on the emissions. Soils were adjusted to a matric potential of –0.5 kPa, and emissions were measured in 3‐hr intervals for 33 days. CO₂ emissions of all soils were similar in the two freeze‐thaw cycles, and followed the temperature course. In contrast, the N₂O emissions during thawing differed considerably. Large N₂O emissions were found on the loamy soil under beech (Loam‐beech) with a maximum N₂O emission of 1200 μg N m^–2 h^–1 and a cumulative emission of 0.15 g N m^–2 in the two thawing periods. However, the sandy soil under beech (Sand‐beech) emitted only 1 mg N₂O‐N m^–2 in the two thawing periods probably because of a low water‐filled pore space of 44 %. The N₂O emissions of the silty soil under beech (Silt‐beech) were small (9 mg N m^–2 in the two thawing periods) with a maximum emission of 150 μg N m^–2 h^–1 while insignificant N₂O emissions were found on the silty soil under spruce (0.2 mg N m^–2 in the two thawing periods). The cumulative N₂O emissions of the short freeze‐thaw cycles were 17 % (Sand‐beech) or 22 % (Loam‐beech, Silt‐beech) less than those of the long freeze‐thaw cycles, but the differences between the emissions of the two periods were not significant (P ≤ 0.05). The results of the study show that the amounts of N₂O emitted in freeze‐thaw cycles vary markedly among different forest soils and that the tree species influence the N₂O thawing emissions in forests considerably due to direct and indirect impacts on soil physical and chemical properties, soil structure, and properties of the humus layer.     

草甸草原模拟氮沉降抑制甲烷吸收、促进氧化亚氮排放

Few studies are conducted to quantify the effects of enhanced N deposition on soil nitrous oxide (N2O) emission and methane (CH4) uptake in the meadow steppe of Inner Mongolia,China.A two-year field experiment was conducted to assess the effects of nitrogen (N) deposition rates (0,10,and 20 kg N ha-1 year-1 as (NH4)2SO4) on soil N2O and CH4 fluxes.The seasonal and diurnal variations of soil N2O and CH4 fluxes were determined using the static chamber-gas chromatography method during the two growing seasons of 2008 and 2009.Soil temperature,moisture and mineral N (NH4+-N and NO3--N) concentration were simultaneously measured.Results showed that low level of (NH4)2SO4 (10 kg N ha-1 year-1) did not significantly affect soil CH4 and N2O fluxes and other variables.High level of (NH4)2SO4 (20 kg N ha-1 year-1) significantly increased soil NO3--N concentration by 24.1％ to 35.6％,decreased soil CH4 uptake by an average of 20.1％,and significantly promoted soil N2O emission by an average of 98.2％.Soil N2O emission responded more strongly to the added N compared to CH4 uptake.However,soil CH4 fluxes were mainly driven by soil moisture,followed by soil NO3--N concentration.Soil N2O fluxes were mainly driven by soil temperature,followed by soil moisture.Soil inorganic N availability was a key integrator of soil CH4 uptake and N2O emission.These results suggest that the changes of availability of inorganic N induced by the increased N deposition in soil may affect the CH4 and N2O fluxes in the cold semi-arid meadow steppe over the short term.