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1.
Conservation tillage practices are widely used to protect against soil erosion and soil C losses, whereas winter cover crops are used mainly to protect against N losses during autumn and winter. For the greenhouse gas balance of a cropping system the effect of reduced tillage and cover crops on N2O emissions may be more important than the effect on soil C. This study monitored emissions of N2O between September 2008 and May 2009 in three tillage treatments, i.e., conventional tillage (CT), reduced tillage (RT) and direct drilling (DD), all with (+CC) or without (−CC) fodder radish as a winter cover crop. Cover crop growth, soil mineral N dynamics, and other soil characteristics were recorded. Furthermore, soil concentrations of N2O were determined eight times during the monitoring period using permanently installed needles. There was little evidence for effects of the cover crop on soil mineral N. Following spring tillage and slurry application soil mineral N was dominated by the input from slurry. Nitrous oxide emissions during autumn, winter and early spring remained low, although higher emissions from +CC treatments were indicated after freezing events. Following spring tillage and slurry application by direct injection N2O emissions were stimulated in all tillage treatments, reaching 250-400 μg N m−2 h−1 except in the CT + CC treatment, where emissions peaked at 900 μg N m−2 h−1. Accumulated emissions ranged from 1.6 to 3.9 kg N2O ha−1. A strong positive interaction between cover crop and tillage was observed. Soil concentration profiles of N2O showed a significant accumulation of N2O in CT relative to RT and DD treatments after spring tillage and slurry application, and a positive interaction between slurry and cover crop residues. A comparison in early May of N2O emissions with flux estimates based on soil concentration profiles indicated that much of the N2O emitted was produced near the soil surface.  相似文献   

2.
Soil compaction and soil moisture are important factors influencing denitrification and N2O emission from fertilized soils. We analyzed the combined effects of these factors on the emission of N2O, N2 and CO2 from undisturbed soil cores fertilized with (150 kg N ha−1) in a laboratory experiment. The soil cores were collected from differently compacted areas in a potato field, i.e. the ridges (ρD=1.03 g cm−3), the interrow area (ρD=1.24 g cm−3), and the tractor compacted interrow area (ρD=1.64 g cm−3), and adjusted to constant soil moisture levels between 40 and 98% water-filled pore space (WFPS).High N2O emissions were a result of denitrification and occurred at a WFPS≥70% in all compaction treatments. N2 production occurred only at the highest soil moisture level (≥90% WFPS) but it was considerably smaller than the N2O-N emission in most cases. There was no soil moisture effect on CO2 emission from the differently compacted soils with the exception of the highest soil moisture level (98% WFPS) of the tractor-compacted soil in which soil respiration was significantly reduced. The maximum N2O emission rates from all treatments occurred after rewetting of dry soil. This rewetting effect increased with the amount of water added. The results show the importance of increased carbon availability and associated respiratory O2 consumption induced by soil drying and rewetting for the emissions of N2O.  相似文献   

3.
Agricultural soils contribute significantly to atmospheric nitrous oxide (N2O). A considerable part of the annual N2O emission may occur during the cold season, possibly supported by high product ratios in denitrification (N2O/(N2+N2O)) and nitrification (N2O-N/(NO3-N+NO2-N)) at low temperatures and/or in response to freeze-thaw perturbation. Water-soluble organic materials released from frost-sensitive catch crops and green manure may further increase winter emissions. We conducted short-term laboratory incubations under standardized moisture and oxygen (O2) conditions, using nitrogen (N) tracers (15N) to determine process rates and sources of emitted N2O after freeze-thaw treatment of soil or after addition of freeze-thaw extract from clover. Soil respiration and N2O production was stimulated by freeze-thaw or addition of plant extract. The N2O emission response was inversely related to O2 concentration, indicating denitrification as the quantitatively prevailing process. Denitrification product ratios in the two studied soils (pH 4.5 and 7.0) remained largely unaltered by freeze-thaw or freeze-thaw-released plant material, refuting the hypothesis that high winter emissions are due to frost damage of N2O reductase activity. Nitrification rates estimated by nitrate (NO3) pool enrichment were 1.5-1.8 μg NO3-N g−1 dw soil d−1 in freeze-thaw-treated soil when incubated at O2 concentrations above 2.3 vol% and one order of magnitude lower at 0.8 vol% O2. Thus, the experiments captured a situation with severely O2-limited nitrification. As expected, the O2 stress at 0.8 vol% resulted in a high nitrification product ratio (0.3 g g−1). Despite this high product ratio, only 4.4% of the measured N2O accumulation originated from nitrification, reaffirming that denitrification was the main N2O source at the various tested O2 concentrations in freeze-thaw-affected soil. N2O emission response to both freeze-thaw and plant extract addition appeared strongly linked to stimulation of carbon (C) respiration, suggesting that freeze-thaw-induced release of decomposable organic C was the major driving force for N2O emissions in our soils, both by fuelling denitrifiers and by depleting O2. The soluble C (applied as plant extract) necessary to induce a CO2 and N2O production rate comparable with that of freeze-thaw was 20-30 μg C g−1 soil dw. This is in the range of estimates for over-winter soluble C loss from catch crops and green manure plots reported in the literature. Thus, freeze-thaw-released organic C from plants may play a significant role in freeze-thaw-related N2O emissions.  相似文献   

4.
The effects of elevated CO2 supply on N2O and CH4 fluxes and biomass production of Phleum pratense were studied in a greenhouse experiment. Three sets of 12 farmed peat soil mesocosms (10 cm dia, 47 cm long) sown with P. pratense and equally distributed in four thermo-controlled greenhouses were fertilised with a commercial fertiliser in order to add 2, 6 or 10 g N m−2. In two of the greenhouses, CO2 concentration was kept at atmospheric concentration (360 μmol mol−1) and in the other two at doubled concentration (720 μmol mol−1). Soil temperature was kept at 15 °C and air temperature at 20 °C. Natural lighting was supported by artificial light and deionized water was used to regulate soil moisture. Forage was harvested and the plants fertilised three times during the basic experiment, followed by an extra fertilisations and harvests. At the end of the experiment CH4 production and CH4 oxidation potentials were determined; roots were collected and the biomass was determined. From the three first harvests the amount of total N in the aboveground biomass was determined. N2O and CH4 exchange was monitored using a closed chamber technique and a gas chromatograph. The highest N2O fluxes (on average, 255 μg N2O m−2 h−1 during period IV) occurred just after fertilisation at high water contents, and especially at the beginning of the growing season (on average, 490 μg N2O m−2 h−1 during period I) when the competition of vegetation for N was low. CH4 fluxes were negligible throughout the experiment, and for all treatments the production and oxidation potentials of CH4 were inconsequential. Especially at the highest rates of fertilisation, the elevated supply of CO2 increased above- and below-ground biomass production, but both at the highest and lowest rates of fertilisation, decreased the total amount of N in the aboveground dry biomass. N2O fluxes tended to be higher under doubled CO2 concentrations, indicating that increasing atmospheric CO2 concentration may affect N and C dynamics in farmed peat soil.  相似文献   

5.
We examined the effects of forest clearfelling on the fluxes of soil CO2, CH4, and N2O in a Sitka spruce (Picea sitchensis (Bong.) Carr.) plantation on an organic-rich peaty gley soil, in Northern England. Soil CO2, CH4, N2O as well as environmental factors such as soil temperature, soil water content, and depth to the water table were recorded in two mature stands for one growing season, at the end of which one of the two stands was felled and one was left as control. Monitoring of the same parameters continued thereafter for a second growing season. For the first 10 months after clearfelling, there was a significant decrease in soil CO2 efflux, with an average efflux rate of 4.0 g m−2 d−1 in the mature stand (40-year) and 2.7 g m−2 d−1 in clearfelled site (CF). Clearfelling turned the soil from a sink (−0.37 mg m−2 d−1) for CH4 to a net source (2.01 mg m−2 d−1). For the same period, soil N2O fluxes averaged 0.57 mg m−2 d−1 in the CF and 0.23 mg m−2 d−1 in the 40-year stand. Clearfelling affected environmental factors and lead to higher daily soil temperatures during the summer period, while it caused an increase in the soil water content and a rise in the water table depth. Despite clearfelling, CO2 remained the dominant greenhouse gas in terms of its greenhouse warming potential.  相似文献   

6.
Nitrogen (N) fertilizer application and grazing are known to induce nitrous oxide (N2O) emissions from grassland soils. In a field study, general information on rates of N2O emission, the effect of cattle grazing and the type (mineral fertilizer, cattle slurry) and amount of N supply on the flux of N2O from a sandy soil were investigated. N2O emissions from permanent grassland managed as a mixed system (two cuts followed by two grazing cycles) were monitored over 11 months during 2001-2002 in northern Germany using the closed chamber method. The field experiment consisted of four regionally relevant fertilizer combinations, i.e. two mineral N application rates (0 and 100 kg N ha−1 yr−1) and two slurry levels (0 and 74 kg N ha−1 yr−1).Mean cumulative N2O-N loss was 3.0 kg ha−1 yr−1, and the cumulative 15N-labelled N2O emissions varied from 0.03% to 0.19% of the 15N applied. 15N labelling indicated that more N2O was emitted from mineral N than from slurry treated plots, and in all treatments the soil N pool was always clearly the major source of N2O. Regarding the total cumulative N2O losses, differences among treatments were not significant, which was caused by: (i) a high variance in emissions during and after cattle grazing due to the random distribution of excrements and by (ii) high N2 fixation of white clover in the 0 kg N ha−1 treatments, which resulted in similar N status of all treatments. However before grazing started, treatments showed significant differences. After cattle grazing in summer, N2O emission rates were higher than around the time of spring fertilizer application, or in winter. Grazing resulted in N2O flux rates up to 489 μg N2O-N m−2 h−1 and the grazing period contributed 31-57% to the cumulative N2O emission. During freeze-thaw cycles in winter (December-February) N2O emission rates of up to 147 μg N2O-N m−2 h−1 were measured, which contributed up to 26% to the annual N2O flux. The results suggest that N fertilizer application and grazing caused only short-term increases of N2O flux rates whereas the major share of annual N2O emission emitted from the soil N pool. The significantly increased N2O fluxes during freeze-thaw cycles show the importance of emission events in winter which need to be covered by measurements for obtaining reliable estimates of annual N2O emissions.  相似文献   

7.
We studied in laboratory microcosms (intact soil cores) N2O and CO2 emissions from four different agricultural soil types (organic soil, clay, silt and loam) at low temperatures with or without freezing-thawing events. When the temperature of the frozen soil cores was increased stepwise from −8 °C the N2O emissions began to increase at −0.5 °C, and peaked at −0.1 °C in the organic, clay and silt soils, and at +1.6 °C in the loam soils. However, a stepwise decrease in soil temperature from +15 °C also induced an increase in the N2O emissions close to the 0 °C. These emissions peaked between −0.4 and +2.5 °C depending on the soil type and water content. However, the emission maxima were from 2 to 14.3% of those encountered in the experiments where frozen soils were thawed. Our results show that in addition to the well-documented thawing peak, soils also can have a maximum in their N2O emission near 0 °C when soil temperature decrease. These emissions, however, are less than those emitted from thawing soils. The correlations between the N2O and CO2 emissions were weak. Our results suggest that N2O is produced in soils down to a temperature of −6 °C.  相似文献   

8.
Nitrous oxide (N2O) is one of the major greenhouse gases emitted from soils, where it is mainly produced by nitrification and denitrification. It is well known that rates of N2O release from soils are mainly determined by the availability of substrates and oxygen, but N2O source apportioning, highly needed to advance N2O mitigation strategies, still remains challenging. In this study, using an automated soil incubation system, the N2O site preference, i.e. the intramolecular 15N distribution, was analyzed to evaluate the progression in N2O source processes following organic soil amendment. Biogas fermentation residue (BGR; originating from food waste fermentation) was applied to repacked grassland soil cores and compared to ammonium sulfate (AS) application, both at rates equivalent to 160 kg NH4+-N ha−1, and to unamended soil (control). The soil cores were incubated in a helium-oxygen atmosphere with 20 kPa O2 for 43 days at 80% water-filled pore space. 43-day cumulative N2O emissions were highest with BGR treated soil accounting for about 1.68 kg N2O-N ha−1 while application of AS caused much lower fluxes of c. 0.23 kg N2O-N ha−1. Also, after BGR application, carbon dioxide (CO2) fluxes showed a pronounced initial peak with steep decline until day 21 whereas with ammonium addition they remained at the background level. N2O dual isotope and isotopomer analysis of gas samples collected from BGR treated soil indicated bacterial denitrification to be the main N2O generating process during the first three weeks when high CO2 fluxes signified high carbon availability. In contrast, in the second half after all added labile carbon substrates had been consumed, nitrification, i.e. the generation of N2O via oxidation of hydroxylamine, gained in importance reaching roughly the same N2O production rate compared to bacterial denitrification as indicated by N2O SP. Overall in this study, bacterial denitrification seemed to be the main N2O forming process after application of biogas residues and fluxes were mainly driven by available organic carbon.  相似文献   

9.
In boreal forests, canopy-scale emissions of biogenic volatile organic compounds (BVOCs) are rather well characterised, but knowledge of ecosystem-scale BVOC emissions is still inadequate. We used adsorbent tubes to measure BVOCs from a boreal Scots pine (Pinus sylvestris L.) forest floor in southern Finland and analysed the compounds with a gas chromatograph-mass spectrometer. The most abundant compound group was the monoterpenes (averaging 5.04 μg m−2 h−1), in which α-pinene, Δ3-carene and camphene contributed over 90% of the emissions. Emissions of other terpenoids (isoprene and sesquiterpenes) were low (averaging 0.05 and 0.04 μg m−2 h−1, respectively). BVOC emissions from the forest floor varied seasonally, peaking in early summer and autumn, with most of the compounds following similar patterns. The emission pattern was sustained throughout the measurement period, suggesting that the main sources of the emissions remained more or less stable. We compared the BVOC fluxes with environmental parameters such as temperature, precipitation and PAR, and with fluxes of other trace gases (CO2, CH4, N2O), as well as with ground vegetation photosynthesis and with litter input. Several of these parameters were correlated with the presence of BVOCs. The sources of soil BVOC emissions are very poorly understood, but our results suggest, that changes in litter quantity and quality, soil microbial activity and the physiological stages of plants are linked with changes in BVOC fluxes.  相似文献   

10.
We examined denitrifying bacteria from wet soils and creek sediment in an agroecosystem in Oregon, USA that received inputs of nitrogen (N) fertilizer. Our objective was to determine the variation in denitrifying community composition and activities across three adjacent habitats: a fertilized agricultural field planted to perennial ryegrass, a naturally vegetated riparian area, and creek sediment. Using C2H2 inhibition, denitrifying enzyme and N2O-reductase activities were determined in short-term incubations of anaerobic slurries. A key gene in the denitrification pathway, N2O reductase (nosZ), served as a marker for denitrifiers. Mean denitrifying enzyme activity (DEA) was similar among habitats, ranging from 0.5 to 1.8 μg N g−1 dry soil h−1. However, the ratio of N2O production, without C2H2, to DEA was substantially higher in riparian soil (0.64±0.02; mean±standard error, n=12) than in agricultural soil (0.19±0.02) or creek sediment (0.32±0.03). Mean N2O-reductase activity ranged from 0.5 to 3.2 μg N g−1 dry soil h−1, with greater activity in agricultural soil than in riparian soil. Denitrifying community composition differed significantly among habitats based on nosZ terminal-restriction fragment length polymorphisms. The creek sediment community was unique. Communities in the agricultural and riparian soil were more closely related but distinct. A number of unique nosZ genotypes were detected in creek sediment. Sequences of nosZ obtained from riparian soil were closely related to nosZ from Bradyrhizobium japonicum. Although nosZ distribution and N2O-reductase activity differed among habitats, relationships between activity and community composition appeared uncoupled across the agroecosystem.  相似文献   

11.
Emissions of N2O and N2 were measured from Lolium perenne L. swards under ambient (36 Pa) and elevated (60 Pa) atmospheric CO2 at the Swiss free air carbon dioxide enrichment experiment following application of 11.2 g N m−2 as 15NH415NO3 or 14NH415NO3 (1 at.% excess 15N). Total denitrification (N2O+N2) was increased under elevated pCO2 with emissions of 6.2 and 19.5 mg 15N m−2 measured over 22 d from ambient and elevated pCO2 swards, respectively, supporting the hypothesis that increased belowground C allocation under elevated pCO2 provides the energy for denitrification. Nitrification was the predominant N2O producing process under ambient pCO2 whereas denitrification was predominant under elevated pCO2. The N2-to-N2O ratio was often higher under elevated pCO2 suggesting that previous estimates of gaseous N losses based only on N2O emissions have greatly underestimated the loss of N by denitrification.  相似文献   

12.
Nitric oxide (NO) and nitrous oxide (N2O) emissions were measured from experimental dung and urine patches placed on boreal pasture soil during two growing seasons and one autumn period until soil freezing. N2O emissions in situ were studied by a static chamber method. NO was measured with a dynamic chamber method using a NO analyser in situ. Mean emissions from the control plots were 47.6±4.5 μg N2ON m−2 h−1 and 12.6±1.6 μg NON m−2 h−1. N2O and NO emissions from urine plots (132±21.2 μg N2ON m−2 h−1 and 51.9±7.6 μg NON m−2 h−1) were higher than those from dung plots (110.0±20.1 μg N2ON m−2 h−1 and 14.7±2.1 μg NON m−2 h−1). There was a large temporal variation in N2O and NO emissions. Maximum N2O emissions were measured a few weeks after dung or urine application, whereas the maximum NO emissions were detected the following year. NO was responsible on average 14% (autumn) and 34% (summer) of total (NO+N2O)N emissions from the pasture soil. NO emissions increased with increasing soil temperature and with decreasing soil moisture. N2O emissions increased with increasing soil moisture, but did not correlate with soil temperature. Therefore we propose that N2O and NO were produced mainly during different microbial processes, i.e., nitrification and denitrification, respectively. The results show that the overall conditions and mechanism especially for emissions of NO are still poorly understood but that there are differences in the mechanisms regulating N2O and NO production.  相似文献   

13.
Reduction of nitrous oxide (N2O) to dinitrogen (N2) by denitrification in soils is of outstanding ecological significance since it is the prevailing natural process converting reactive nitrogen back into inert molecular dinitrogen. Furthermore, the extent to which N2O is reduced to N2 via denitrification is a major regulating factor affecting the magnitude of N2O emission from soils. However, due to methodological problems in the past, extremely little information is available on N2 emission and the N2:N2O emission ratio for soils of terrestrial ecosystems. In this study, we simultaneously determined N2 and N2O emissions from intact soil cores taken from a mountainous beech forest ecosystem. The soil cores were taken from plots with distinct differences in microclimate (warm-dry versus cool-moist) and silvicultural treatment (untreated control versus heavy thinning). Due to different microclimates, the plots showed pronounced differences in pH values (range: 6.3–7.3). N2O emission from the soil cores was generally very low (2.0 ± 0.5–6.3 ± 3.8 μg N m−2 h−1 at the warm-dry site and 7.1 ± 3.1–57.4 ± 28.5 μg N m−2 h−1 at the cool-moist site), thus confirming results from field measurements. However, N2 emission exceeded N2O emission by a factor of 21 ± 6–220 ± 122 at the investigated plots. This illustrates that the dominant end product of denitrification at our plots and under the given environmental conditions is N2 rather than N2O. N2 emission showed a huge variability (range: 161 ± 64–1070 ± 499 μg N m−2 h−1), so that potential effects of microclimate or silvicultural treatment on N2 emission could not be identified with certainty. However, there was a significant effect of microclimate on the magnitude of N2O emission as well as on the mean N2:N2O emission ratio. N2:N2O emission ratios were higher and N2O emissions were lower for soil cores taken from the plots with warm-dry microclimate as compared to soil cores taken from the cool-moist microclimate plots. We hypothesize that the increase in the N2:N2O emission ratio at the warm-dry site was due to higher N2O reductase activity provoked by the higher soil pH value of this site. Overall, the results of this study show that the N2:N2O emission ratio is crucial for understanding the regulation of N2O fluxes of the investigated soil and that reliable estimates of N2 emissions are an indispensable prerequisite for accurately calculating total N gas budgets for the investigated ecosystem and very likely for many other terrestrial upland ecosystems as well.  相似文献   

14.
Denitrification rates are often greater in no-till than in tilled soils and net soil-surface greenhouse gas emissions could be increased by enhanced soil N2O emissions following adoption of no-till. The objective of this study was to summarize published experimental results to assess whether the response of soil N2O fluxes to the adoption of no-till is influenced by soil aeration. A total of 25 field studies presenting direct comparisons between conventional tillage and no-till (approximately 45 site-years of data) were reviewed and grouped according to soil aeration status estimated using drainage class and precipitation during the growing season. The summary showed that no-till generally increased N2O emissions in poorly-aerated soils but was neutral in soils with good and medium aeration. On average, soil N2O emissions under no-till were 0.06 kg N ha−1 lower, 0.12 kg N ha−1 higher and 2.00 kg N ha−1 higher than under tilled soils with good, medium and poor aeration, respectively. Our results therefore suggest that the impact of no-till on N2O emissions is small in well-aerated soils but most often positive in soils where aeration is reduced by conditions or properties restricting drainage. Considering typical soil C gains following adoption of no-till, we conclude that increased N2O losses may result in a negative greenhouse gas balance for many poorly-drained fine-textured agricultural soils under no-till located in regions with a humid climate.  相似文献   

15.
In order to investigate the diurnal, seasonal, and inter-annual variations of nitrous oxide (N2O) flux and associated microbiological mechanisms, in situ measurements of N2O Flux from unfertilized, ungrazed, and unirrigated semi-arid grassland soils in Inner Mongolia, northeast China were undertaken using a closed chamber technique from 1995 to 2003. In addition, laboratory experiments were carried out using the acetylene inhibition method (AIM) in 1998 and 2001. The results showed no significant linear relationship between soil moisture and diurnal N2O flux, or between N2O flux and temperature (i.e., temperature at 0-15 cm depth, temperature of surface soil, and temperature of inner chamber air). However, the results showed a significant influence of growing season on diurnal variations of N2O flux. N2O efflux was usually high in spring or summer, and low in winter. The mean total annual N2O fluxes was 0.73±0.52 kg N2O-N ha−1 yr−1, with a coefficient of variation of annual N2O flux of 71.6%. Based on our estimates from 5 yr of data, the total N2O emission from all of the temperate grassland soils of China was approximately 0.21 Tg N2O-N yr−1, which was about 21% of the total global flux from temperate grassland soils. It was the distribution of effective rainfall, rather than precipitation intensity, that influenced seasonal and inter-annual variations of N2O flux. Our laboratory incubation study revealed that heterotrophic nitrification was the principal source of N2O in the studied soils.  相似文献   

16.
Emissions of N2O and CH4 and CH4 oxidation rates were measured from Lolium perenne swards in a short-term study under ambient (36 Pa) and elevated (60 Pa) atmospheric CO2 at the Free Air Carbon dioxide Enrichment experiment, Eschikon, Switzerland. Elevated pCO2 increased (P<0.05) N2O emissions from high N fertilised (11.2 g N m−2) swards by 69%, but had no significant effect on net emissions of CH4. Application of 13C-CH4 (11 μl l−1; 11 at.% excess 13C) to closed chamber headspaces in microplots enabled determination of rates of 13C-CH4 oxidation even when net CH4 fluxes from main plots were positive. We found a significant interaction between fertiliser application rate and atmospheric pCO2 on 13C-CH4 oxidation rates that was attributed to differences in gross nitrification rates and C and N availability. CH4 oxidation was slower and thought to be temporarily inhibited in the high N ambient pCO2 sward. The most rapid CH4 oxidation of 14.6 μg 13C-CH4 m−2 h−1 was measured in the high fertilised elevated pCO2 sward, and we concluded that either elevated pCO2 had a stimulatory effect on CH4 oxidation or inhibition of oxidation following fertiliser application was lowered under elevated pCO2. Application of 14NH415NO3 and 15NH415NO3 (10 at.% excess 15N) to different replicates enabled determination of the respective contributions of nitrification and denitrification to N2O emissions. Inhibition of CH4 oxidation in the high fertilised ambient pCO2 sward, due to competition between NH3 and CH4 for methane monooxygenase enzymes or toxic effects of NH2OH or NO2 produced during nitrification, was hypothesised to increase gross nitrification (12.0 mg N kg dry soil−1) and N2O emissions during nitrification (327 mg 15N-N2O m−2 over 11 d). Our results indicate that increasing atmospheric concentrations of CO2 may increase emissions of N2O by denitrification, lower nitrification rates and either increase or decrease the ability of soil to act as a sink for atmospheric CH4 depending on fertiliser management.  相似文献   

17.
Nitrous oxide (N2O) is a greenhouse gas and agricultural soils are major sources of atmospheric N2O. Its emissions from soils make up the largest part in the global N2O budget. Research was carried out at the experimental fields of the Leibniz-Institute of Agricultural Engineering Potsdam-Bornim (ATB). Different types (mineral and wood ash) and levels (0, 75 and 150 kg N ha−1) of fertilization were applied to annual (rape, rye, triticale and hemp) and perennial (poplar and willow) plants every year. N2O flux measurements were performed 4 times a week by means of gas flux chambers and an automated gas chromatograph between 2003 and 2005. Soil samples were also taken close to the corresponding measuring rings. Soil nitrate and ammonium were measured in soil extracts.N2O emissions had a peak after N fertilization in spring, after plant harvest in summer and during the freezing–thawing periods in winter. Both fertilization and plant types significantly altered N2O emission. The maximum N2O emission rate detected was 1081 μg N2O m−2 h−1 in 2004. The mean annual N2O emissions from the annual plants were more than twofold greater than those of perennial plants (4.3 kg ha−1 vs. 1.9 kg ha−1). During January, N2O fluxes considerably increased in all treatments due to freezing–thawing cycles. Fertilization together with annual cropping doubled the N2O emissions compared to perennial crops indicating that N use efficiency was greater for perennial plants. Fertilizer-derived N2O fluxes constituted about 32% (willow) to 67% (rape/rye) of total soil N2O flux. Concurrent measurements of soil water content, NO3 and NH4 support the conclusion that nitrification is main source of N2O loss from the study soils. The mean soil NO3-N values of soils during the study for fertilized soils were 1.6 and 0.9 mg NO3-N kg−1 for 150 and 75 kg N ha−1 fertilization, respectively. This value reduced to 0.5 mg NO3-N kg−1 for non-fertilized soils.  相似文献   

18.
The effects of compaction on soil porosity and soil water relations are likely to influence substrate availability and microbial activity under fluctuating soil moisture conditions. We conducted a short laboratory incubation to investigate the effects of soil compaction on substrate availability and biogenic gas (CO2 and N2O) production during the drying and rewetting of a fine-loamy soil. Prior to initiating the drying and wetting treatments, CO2 production (−10 kPa soil water content) from uncompacted soil was 2.3 times that of compacted soil and corresponded with higher concentrations of microbial biomass C (MBC) and dissolved organic C (DOC). In contrast, N2O production was 67 times higher in compacted than uncompacted soil at field capacity. Soil aeration rather than substrate availability (e.g. NO3 and DOC) appeared to be the most important factor affecting N2O production during this phase. The drying of compacted soil resulted in an initial increase in CO2 production and a nearly two-fold higher average rate of C mineralization at maximum dryness (owing to a higher water-filled pore space [WFPS]) compared to uncompacted soil. During the drying phase, N2O production was markedly reduced (by 93-96%) in both soils, though total N2O production remained slightly higher in compacted than uncompacted soil. The increase in CO2 production during the first 24 h following rewetting of dry soil was about 2.5 times higher in uncompacted soil and corresponded with a much greater release of DOC than in compacted soil. MBC appeared to be the source of the DOC released from uncompacted soil but not from compacted soil. The production of N2O during the first 24 h following rewetting of dry soil was nearly 20 times higher in compacted than uncompacted soil. Our results suggest that N2O production from compacted soil was primarily the result of denitrification, which was limited by substrates (especially NO3) made available during drying and rewetting and occurred rapidly after the onset of anoxic conditions during the rewetting phase. In contrast, N2O production from uncompacted soil appeared to be primarily the product of nitrification that was largely associated with an accumulation of NO3 following rewetting of dry soil. Irrespective of compaction, the response to drying and rewetting was greater for N2O production than for CO2 production.  相似文献   

19.
The greenhouse gases CO2 and N2O emissions were quantified in a long-term experiment in northern France, in which no-till (NT) and conventional tillage (CT) had been differentiated during 32 years in plots under a maize–wheat rotation. Continuous CO2 and periodical N2O soil emission measurements were performed during two periods: under maize cultivation (April 2003–July 2003) and during the fallow period after wheat harvest (August 2003–March 2004). In order to document the dynamics and importance of these emissions, soil organic C and mineral N, residue decomposition, soil potential for CO2 emission and climatic data were measured. CO2 emissions were significantly larger in NT on 53% and in CT on 6% of the days. From April to July 2003 and from November 2003 to March 2004, the cumulated CO2 emissions did not differ significantly between CT and NT. However, the cumulated CO2 emissions from August to November 2003 were considerably larger for NT than for CT. Over the entire 331 days of measurement, CT and NT emitted 3160 ± 269 and 4064 ± 138 kg CO2-C ha−1, respectively. The differences in CO2 emissions in the two tillage systems resulted from the soil climatic conditions and the amounts and location of crop residues and SOM. A large proportion of the CO2 emissions in NT over the entire measurement period was probably due to the decomposition of old weathered residues. NT tended to emit more N2O than CT over the entire measurement period. However differences were statistically significant in only half of the cases due to important variability. N2O emissions were generally less than 5 g N ha−1 day−1, except for a few dates where emission increased up to 21 g N ha−1 day−1. These N2O fluxes represented 0.80 ± 0.15 and 1.32 ± 0.52 kg N2O-N ha−1 year−1 for CT and NT, respectively. Depending on the periods, a large part of the N2O emissions occurred was probably induced by nitrification, since soil conditions were not favorable for denitrification. Finally, for the period of measurement after 32 years of tillage treatments, the NT system emitted more greenhouses gases (CO2 and N2O) to the atmosphere on an annual basis than the CT system.  相似文献   

20.
After implementation of legislative measures for the reduction of environmental hazards from nitrate leaching and ammonia volatilisation when using organic manures and fertilizers in Europe, much attention is now paid to the specific effects of these fertilizers on the dynamics of global warming-relevant trace gases in soil. Particularly nitrogen fertilizers and slurry from animal husbandry are known to play a key role for the CH4 and N2O fluxes from soils. Here we report on a short-term evaluation of trace gas fluxes in grassland as affected by single or combined application of mineral fertilizer and organic manure in early spring. Methane fluxes were characterised by a short methane emission event immediately after application of cattle slurry. Within the same day methane fluxes returned to negative, and on average over the 4-day period after slurry application, only a small but insignificant trend to reduced methane oxidation was found. Nitrous oxide emissions showed a pronounced effect of combined slurry and mineral fertilizer application. In particular fresh cattle slurry combined with calcium ammonium nitrate (CAN) mineral fertilizer induced an increase in mean N2O flux during the first 4 days after application from 10 to 300 μg N2O-N m−2 h−1. 15N analysis of emitted N2O from 15N-labelled fertilizer or manure indicated that easily decomposable slurry C compounds induced a pronounced promotion of N2O-N emission derived from mineral CAN fertilizer. Fluxes after application of either mineral fertilizer or slurry alone showed an increase of less than 5-fold. The NOx sink strength of the soil was in the range of −6 to −10 μg NOx-N m−2 h−1 and after fertilization it showed a tendency to be reduced by no more than 2 μg NOx-N m−2 h−1, which was a result of both, increased NO emission and slightly increased NO2 deposition. Associated determination of the N2O:N2 emission ratio revealed that after mineral N application (CAN) a large proportion (c. 50%) was emitted as N2O, while after application of slurry with easily decomposable C and predominantly -N serving as N-source, the N2O:N2 emission ratio was 1:14, i.e. was changed in favour of N2. Our work provides evidence that particularly the combination of slurry and nitrate-containing N fertilizers gives rise to considerable N2O emissions from mineral fertilizer N pool.  相似文献   

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