Nitrous oxide emission from frozen grassland soil and during thawing periods

Nitrous oxide (N₂O) was emitted during a frost period from an old grassland as well as during thawing. Soil incubations at various times throughout the freezing period showed that highest emission rates were emitted around 0 °C, and the magnitude of the emission peak increased with the length of the freezing period. Highest N₂O emissions during freezing and thawing were measured from soil previously treated with nitrate (NO₃^‐). The emitted N₂O was produced via reduction of NO₃^‐. The steady drop in N₂O emission at soil temperatures higher than 2 °C coincided with large dinitrogen (N₂) emissions which most likely reflected the increasing enzymatic activity of N₂O reductase with increasing temperatures. Measurements of mineral N concentrations showed that NO₃^‐ and NH₄⁺, which were shortly after fertilizer application immobilized into the microbial biomass, became partly available again through the freezing effect and caused large N₂O emissions in winter. This study provided evidence that N₂O emissions during freezing and thawing in the winter are due to biological rather than chemical activity in soil.     

Modelling soil organic matter decomposition and rainfall erosion in two tropical soils after forest clearing for permanent agriculture

A soil organic matter turnover model has been developed to analyse soil carbon (soil organic-C) loss caused by organic matter decomposition and rainfall erosion in soils used for permanent cultivation. It has been used to build up model profiles of five soils, one occurring in temperate and four in tropical regions, on the basis of estimates for ‘natural’ organic matter input. Organic matter input data for different systems of cultivation were used to model the long-term decomposition of soil organic-C in these model profiles. The modelling results show that soil organic matter decomposition in the tropics is three to four times faster than in temperate regions, and that there is a marked influence of soil type and soil climate. Simulated losses of organic-C in the tropical soils, not accounting for erosion are 31 to 50 per cent after 50 years and 43 to 63 per cent after 100 years of continuous cultivation. The simulated loss of soil organic-C when rainfall erosion is also allowed for is 40 to 80 per cent. Erosion caused an extra loss of at least 7 per cent after 100 years. The initial input of charcoal from forest burning is lost through erosion at a rate of 50 to almost 100 per cent, depending on the severity of erosion. The sensitivity of modelling results to variations in input data was also analysed. The losses of soil carbon were also used to calculate the global flux of CO₂ from soils. Soils are probably a small but not negligible source of CO₂.     

Effect of plant-mediated oxygen supply and drainage on greenhouse gas emission from a tropical peatland in Central Kalimantan,Indonesia

Abstract

To evaluate the hypothesis that plant-mediated oxygen supplies decrease methane (CH₄) production and total global warming potential (GWP) in a tropical peatland, the authors compared the fluxes and dissolved concentrations of greenhouse gases [GHGs; CH₄, carbon dioxide (CO₂) and nitrous oxide (N₂O)] and dissolved oxygen (DO) at multiple peatland ecosystems in Central Kalimantan, Indonesia. Study ecosystems included tropical peat swamp forest and degraded peatland areas that were burned and/or drained during the rainy season. CH₄ fluxes were significantly influenced by land use and drainage, which were highest in the flooded burnt sites (5.75 ± 6.66 mg C m^?2 h^?1) followed by the flooded forest sites (1.37 ± 2.03 mg C m^?2 h^?1), the drained burnt site (0.220 ± 0.143 mg C m^?2 h^?1), and the drained forest site (0.0084 ± 0.0321 mg C m^?2 h^?1). Dissolved CH₄ concentrations were also significantly affected by land use and drainage, which were highest in the flooded burnt sites (124 ± 84 μmol L^?1) followed by the drained burnt site (45.2 ± 29.8 μmol L^?1), the flooded forest sites (1.15 ± 1.38 μmol L^?1) and the drained forest site (0.860 ± 0.819 μmol L^?1). DO concentrations were influenced by land use only, which were significantly higher in the forest sites (6.9 ± 5.6 μmol L^?1) compared to the burnt sites (4.0 ± 2.9 μmol L^?1). These results suggest that CH₄ produced in the peat might be oxidized by plant-mediated oxygen supply in the forest sites. CO₂ fluxes were significantly higher in the drained forest site (340 ± 250 mg C m^?2 h^?1 with a water table level of ?20 to ?60 cm) than in the drained burnt site (108 ± 115 mg C m^?2 h^?1 with a water table level of ?15 to +10 cm). Dissolved CO₂ concentrations were 0.6–3.5 mmol L^?1, also highest in the drained forest site. These results suggested enhanced CO₂ emission by aerobic peat decomposition and plant respiration in the drained forest site. N₂O fluxes ranged from ?2.4 to ?8.7 μg N m^?2 h^?1 in the flooded sites and from 3.4 to 8.1 μg N m^?2 h^?1 in the drained sites. The negative N₂O fluxes might be caused by N₂O consumption by denitrification under flooded conditions. Dissolved N₂O concentrations were 0.005–0.22 μmol L^?1 but occurred at < 0.01 μmol L^?1 in most cases. GWP was mainly determined by CO₂ flux, with the highest levels in the drained forest site. Despite having almost the same CO₂ flux, GWP in the flooded burnt sites was 20% higher than that in the flooded forest sites due to the large CH₄ emission (not significant). N₂O fluxes made little contribution to GWP.     

Interactive effects of ammonium application rates and temperature on nitrous oxide emission from tropical agricultural soil

Emissions of nitrous oxide (N₂O), a potent greenhouse gas, from agricultural soil have been recognized to be affected by nitrogen (N) application and temperature. Most of the previous studies were carried out to determine effects of temperature on N₂O emissions at a fixed N application rate or those of N application rates at a specific temperature. Knowledge about the effects of different ammonium (NH₄⁺) application rates and temperatures on N₂O emissions from tropical agricultural soil and their interactions is limited. Five grams of air-dried sandy loam soil, collected in Central Vietnam, were adjusted to 0, 400, 800 and 1200 mg NH₄-N kg^–1 soil (abbreviated as 0 N, 400 N, 800 N and 1200 N, respectively) at 60% water holding capacity were aerobically incubated at 20°C, 25°C, 30°C or 35°C for 28 days. Mineral N contents and N₂O emission rates were determined on days 1, 3, 5, 7, 14, 21 and 28. Cumulative N₂O emissions for 28 days increased with increasing NH₄⁺ application rates from 0 to 800 mg N kg^–1 and then declined to 1200 mg N kg^–1. Cumulative N₂O emissions increased in the order of 35°C, 20°C, 30°C and 25°C. This lowest emission at 35°C occurred because N₂O production was derived only from autotrophic nitrification while other N₂O production processes, e.g., nitrifier denitrification and coupled nitrification-denitrification occurred at lower temperatures. More specifically, cumulative N₂O emissions peaked at 800 N and 25°C, and the lowest emissions occurred at 1200 N and 35°C. In conclusion, N₂O emissions were not exponentially correlated with NH₄⁺ application rates or temperatures. Higher NH₄⁺ application rates at higher temperatures suppressed N₂O emissions.     

蚯蚓对红壤有机质分解的影响

The earthworms Pheretima carnosa, Drawida gisti and Eisenia foetida were studied to compare their contributions to the decomposition of various organic materials surface-applied on red soil in a 165-day greenhouse experiment. The native species Pheretima carnosa and Drawida gisti were equally effective in accelerating the decomposition of maize residue, according to fresh body weight, while commercial species Eisenia foetida had no significant influence on dry mass loss of maize residue. Liming with CaCO3 or CaO showed little effect on maize residue breakdown involved by Pheretima carnosa, but it inhibited this process involved by Drawida gisti. The capability of Pheretima carnosa to the decomposition of five kinds of organic materials was thoroughly examined. The dry mass losses in worm treatments were in the order of soybean residue ＞ maize residue ＞ pig manure ＞ semi-decayed maize ＞ ryegrass. However, the relative contributions of the earthworm to dry mass loss were in the order of pig manure (89.8%) ＞ semi-decayed maize residue (49.1%) ＞ maize residue (29.4%) ＞ soybean residue (20.9%) ＞ ryegrass residue (16.5%). Pheretima carnosa consumed 20～120 mg dry weight of organic material per gram fresh weight of biomass per day.     

Effect of crop residue incorporation on soil organic carbon and greenhouse gas emissions in European agricultural soils

Soil organic matter (SOM) improves soil physicochemical and biological properties, and the sequestration of carbon in SOM may mitigate climate change. Soil organic carbon (SOC) often decreases in intensive cropping systems. Incorporation of crop residues (CR) may be a sustainable management practice to maintain the SOC levels and to increase soil fertility. This study quantifies the effects of CR incorporation on SOC and greenhouse gas (GHG) emissions (CO₂ and N₂O) in Europe using data from long‐term experiments. Response ratios (RRs) for SOC and GHG emissions were calculated between CR incorporation and removal. The influence of environmental zones (ENZs), clay content and experiment duration on the RRs was investigated. We also studied how RRs of SOC and crop yields were correlated. A total of 475 RRs were derived from 39 publications. The SOC increased by 7% following CR incorporation. In contrast, in a subsample of cases, CO₂ emissions were six times and N₂O emissions 12 times higher following CR incorporation. The ENZ had no significant influence on RRs. For SOC concentration, soils with a clay content >35% showed 8% higher RRs compared with soils with clay contents between 18 and 35%. As the experiment progressed, RR for SOC concentration increased. For N₂O emissions, RR was significantly greater in experiments with a duration <5 yr compared with 11–20 yr. No significant correlations were found between RR for SOC concentration and yields, but differences between sites and study durations were detected. We suggest that a long duration of crop residue incorporation is a win‐win scenario under a continental climate. We conclude that CR incorporation is important for maintaining SOC, but its influence on GHG emissions should be taken into account as well.     

Fungal N2O production in an arable peat soil in Central Kalimantan,Indonesia

Abstract

To clarify the microbiological factors that explain high N₂O emission in an arable peat soil in Central Kalimantan, Indonesia, a substrate-induced respiration-inhibition experiment was conducted for N₂O production. The N₂O emission rate decreased by 31% with the addition of streptomycin, whereas it decreased by 81% with the addition of cycloheximide, compared with a non-antibiotic-added control. This result revealed a greater contribution of the fungal community than bacterial community to the production of N₂O in the soil. The population density of fungi in the soil, determined using the dilution plate method, was 5.5 log c.f.u. g^?1 soil and 4.9 log c.f.u. g^?1 soil in the non-selective medium (rose bengal) and the selective medium for Fusarium, respectively. The N₂O-producing potential was randomly examined in each of these isolates by inoculation onto Czapek agar medium (pH 4.3) and incubation at 28°C for 14 days. Significant N₂O-producing potential was found in six out of 19 strains and in five out of seven strains isolated from the non-selective and selective media, respectively. Twenty-three out of 26 strains produced more than 20% CO₂ during the 14-day incubation period, suggesting the presence of facultative fungi in the soil. These strains were identified to be Fusarium oxysporum and Neocosmospora vasinfecta based on the sequence of 18S rDNA, irrespective of the N₂O-producing potential and the growth potential in conditions of low O₂ concentration.     

Nitrous oxide emission as affected by changes in soil water content and nitrogen fertilization

Nitrous oxide emission was measured in laboratory incubations of an alluvial soil (58% clay, pH 7.4). The soil was amended with 40 mg N kg⁻¹ as NaNO₃ or NH₄Cl, or with NaCl as a control. Each fertilization treatment was adjusted to three different water contents: constant 60% WHC (water-holding capacity), constant 120% WHC, and water content alternating between 60 and 120% WHC. During an 8-day incubation period N₂O emission rates and inorganic nitrogen concentrations in soil (NH₄⁺, NO₂⁻, NO₃⁻) were determined at regular intervals. In the control and after nitrate application small N₂O emission rates occurred with only minor variations over time, and no differences between the water treatments. In contrast, with ammonium application N₂O emission rates were much higher during the first two days of incubation, with peaks in the constant 60% WHC and 120% WHC at day 1 and in the changing-water treatment at day 2, when the first wet period (120% WHC) was completed. This N₂O peak in the changing-water treatment was 4 to 9 times higher than with constant WHC and occurred when both, NH₄⁺ and NO₂⁻ concentrations declined sharply. Thus, this N₂O emission flush can be attributed to nitrifier denitrification. After the second rewetting of the NH₄⁺-amended soil no further N₂O emission peak was observed, being in accordance with small NH₄⁺ and NO₂⁻ concentrations in soil at that time. The unexpectedly small N₂O fluxes in the constant 120% WHC treatment after nitrate application were probably caused by the reduction of N₂O to N₂ under the prevailing conditions. It can be concluded that continuous wetting or flooding of a soil is an effective measure to reduce N₂O emissions immediately after the application of NH₄⁺ fertilizers.     

Labile and stable pools of organic matter in soil amended with sewage sludge biochar

One of the main advantages of using biochar for agricultural purposes is its ability to store carbon (C) in soil for a long-term. Studies of labile and stable fractions of soil organic matter (SOM) may be a good indicator of the dynamics of biochar in soils. This study evaluated the effects of applying sewage sludge biochar (SSB) in combination with mineral fertilizer on fractions of SOM. To conduct this evaluation, 15 Mg ha^?1 of SSB combined or not with mineral fertilizer (NPK) was applied to the soil in two cropping seasons. Apart from total organic C (TOC), the labile and stable fractions of SOM were also determined. The combined use of SSB and NPK resulted in higher TOC, a 22% to 40% increase compared to the control and to the NPK treatments, respectively. The SSB produced at a lower temperature increased the labile fractions of SOM, especially the microbial biomass C, showing its capacity to supply nutrients in the short-term. The stable pools of SOM are increased after adding SSB produced at a higher temperature. It was concluded that pyrolysis temperature is a key-factor that determines the potential of SSB to accumulate C in labile and stable fractions of SOM.     

Temperature sensitivity of soil organic matter decomposition varies with biochar application and soil type

Biochar application has the potential to improve soil fertility and increase soil carbon stock, especially in tropical regions. Information on the temperature sensitivity of carbon dioxide(CO_2) evolution from biochar-amended soils at very high temperatures, as observed for tropical surface soils, is limited but urgently needed for the development of region-specific biochar management targeted to optimize biochar effects on soil functions. Here, we investigated the temperature sensitivity of soil respiration to the addition of different rates of Miscanthus biochar(0, 6.25, 12.5, and 25 Mg ha~(-1)) in two types of soils with contrasting textures. Biochar-amended soil treatments and their controls were incubated at constant temperatures of 20, 30, and 40℃. Overall, our results show that: i) considering data from all treatments and temperatures, the addition of biochar decreased soil CO_2 emissions when compared to untreated soils;ii) CO_2 emissions from biochar-amended soils had a higher temperature sensitivity than those from biochar-free soils; iii) the temperature sensitivity of soil respiration in sandy soils was higher than that in clay soils; and iv) for clay soils, relative increases in soil CO_2 emissions from biochar-amended soils were higher when the temperature increased from 30 to 40℃, while for sandy soils, the highest temperature responses of soil respiration were observed when increasing the temperature from 20 to 30℃. Together, these findings suggest a significantly reduced potential to increase soil organic carbon stocks when Miscanthus biochar is applied to tropical soils at high surface temperatures, which could be counteracted by the soil-and weather-specific timing of biochar application.     

Direct effects of litter decomposition on soil dissolved organic carbon and nitrogen in a tropical rainforest

To clarify how litter decomposition processes affect soil dissolved organic carbon (DOC) and soil dissolved nitrogen (DN) dynamics, we conducted a field experiment on leaf litter and collected DOC and DN from the underlying soil in a tropical rainforest in Xishuangbanna, southwest China. Principal components analysis (PCA) showed the first PCA axis (corresponding to degraded litter quantity and quality) explained 61.3% and 71.2% of variation in DOC and DN concentrations, respectively. Stepwise linear regression analysis indicated that litter carbon mass controlled DOC and hemicellulose mass controlled DN concentrations. Litter decomposition was the predominant factor controlling surface-soil DOC and DN dynamics in this tropical rainforest.     

Phenol oxidase, peroxidase and organic matter dynamics of soil

Extracellular enzymes mediate the degradation, transformation and mineralization of soil organic matter. The activity of cellulases, phosphatases and other hydrolases has received extensive study and in many cases stoichiometric relationships and responses to disturbances are well established. In contrast, phenol oxidase and peroxidase activities, which are often uncorrelated with hydrolase activities, have been measured in only a small subset of soil enzyme studies. These enzymes are expressed for a variety of purposes including ontogeny, defense and the acquisition of carbon and nitrogen. Through excretion or lysis, these enzymes enter the environment where their aggegrate activity mediates key ecosystem functions of lignin degradation, humification, carbon mineralization and dissolved organic carbon export. Phenol oxidases and peroxidases are less stable in the environment than extracellular hydrolases, especially when associated with organic particles. Activities are also affected, positively and negatively, by interaction with mineral surfaces. High spatiotemporal variation obscures their relationships with environmental variables and ecological process. Across ecosystems, phenol oxidase and peroxidase activities generally increase with soil pH, a finding not predicted from the pH optima of purified enzymes. Activities associated with plant litter and particulate organic matter often correlate with decomposition rates and potential activities generally increase with the lignin and secondary compound content of the material. At the ecosystem scale, nitrogen amendment alters the expression of phenol oxidase and peroxidase enzymes more broadly than culture studies imply and these responses correlate with positive and negative changes in litter decomposition rates and soil organic matter content. At the global scale, N amendment of basidiomycete-dominated soils of temperate and boreal forest ecoystems often leads to losses of oxidative enzyme activity, while activities in grassland soils dominated by glomeromycota and ascomycetes show little net response. Land use that leads to loss of soil organic matter tends to increase oxidative activities. Across ecosystems, soil organic matter content is not correlated with mean potential phenol oxidase and peroxidase activities. A multiple regression model that includes soil pH, mean annual temperature, mean annual precipitation and potential phenol oxidase activity accounts for 37% of the variation in soil organic matter (SOM) content across ecosystems (n = 63); a similar model for peroxidase activity describes 32% of SOM variance (n = 43). Analysis of residual variation suggest that suites of interacting factors create both positive and negative feedbacks on soil organic matter storage. Soils with high oxygen availability, pH and mineral activity tend to be substrate limited: high in situ oxidative activities limit soil organic matter accumulation. Soils with opposing characteristics are activity limited: low in situ oxidative activities promote soil organic matter storage.     

Lime-nitrogen application reduces N2O emission from a vegetable field with imperfectly-drained sandy clay-loam soil

Abstract

We studied the effect of lime-nitrogen (calcium cyanamide, CaCN₂) application on the emission of nitrous oxide (N₂O) from a vegetable field with imperfectly-drained sandy clay-loam soil. Lime-nitrogen acts as both a pesticide and a fertilizer. During the decomposition of lime-nitrogen in the soil, dicyandiamide (DCD), a nitrification inhibitor, is formed, and as a result lime-nitrogen application may mitigate N₂O emission from the soil. The study design consisted of three different nitrogen-application treatments in field plots with a randomized block design. The nitrogen application treatments were: CF (chemical fertilizer), LN (all nitrogen fertilizer applied as lime-nitrogen), and CFD (chemical fertilizer containing DCD). Soil nitrification activity was lower in the LN and CFD plots than in the CF plots, and nitrification was inhibited for a longer period in the LN plots than in the CFD plots. In the LN plots, N₂O emission was lower than those of other treatments from 20 to 40 days after fertilization, a period when large peaks of N₂O emission were observed after rainfall in the CF and CFD plots. Cumulative N₂O emission over 63 days in the CF plots (mean ± standard deviation: 30.2 ± 14.4 mg N₂O m^?2) and CFD plots (24.3 ± 10.8 mg N₂O m^?2) was significantly higher than that in the LN plots (10.7 ± 1.2 mg N₂O m^?2; P < 0.05). Our results suggested that lime-nitrogen application decreased N₂O emission by inhibiting both nitrification and denitrification.     

Carbon and nitrogen in operationally defined soil organic matter pools

Humic substances [humic acid (HA), fulvic acid (FA), and insoluble humin], particulate organic matter (POM), and glomalin comprise the majority (ca 75%) of operationally defined extractable soil organic matter (SOM). The purpose of this work was to compare amounts of carbon (C) and nitrogen (N) in HA, FA, POM, and glomalin pools in six undisturbed soils. POM, glomalin, HA, and FA in POM, and glomalin, HA, and FA in POM-free soil were extracted in the following sequence: (1) POM fraction separation from the soil, (2) glomalin extraction from the POM fraction and POM-free soil, and (3) co-extraction of HA and FA from the POM fraction and POM-free soil. Only trace amounts of HA and FA were present in the POM fraction, while POM-associated glomalin (POM-glomalin) and POM alone contributed 2 and 12%, respectively, of the total C in the soil. Mean combined weights for chemically extracted pools from POM and from POM-free soil were 9.92 g glomalin, 1.12 g HA, and 0.88 g FA kg⁻¹ soil. Total protein and C, N, and H concentrations showed that glomalin and HA were, for the most part, separate pools, although protein was detected in HA extracts. Even though percentage carbon was higher in HA than in glomalin, glomalin was a larger (almost nine times) operationally defined pool of soil organic C. Glomalin was also the largest pool of soil N of all the pools isolated, but all pools combined only contained 31% of the total N in the soil.     

中国土壤有机碳分解特征研究初报

通过土壤样品的室内培养,运用三库一级动力学理论,对我国典型区域土壤有机碳分解特征进行了研究,结果表明:土壤有机碳分解均呈现前期分解快速和后期分解缓慢的特点,土壤有机碳分解的平衡点大概为2个月,之后的日均分解量变化非常小。我国东部4种地带性土壤有机碳分解速率随纬度的增加而递增。不同种植方式农田土壤有机碳分解速率:菜园>水田>旱地>果园。6个地区表层土壤有机碳含量范围为2.31~81.93 g/kg;活性碳含量范围为0.09~1.04 g/kg;缓效性碳含量范围为0.90~33.39 g/kg;惰效性碳含量范围0.92~47.85 g/kg。     

Effects of organic matter addition on phosphorus availability to flooded and nonflooded rice in a P‐deficient tropical soil: a greenhouse study

Addition of organic matter (OM) to flooded soils stimulates reductive dissolution of Fe(III) minerals, thereby mobilizing associated phosphate (P). Hence, OM management has the potential to overcome P deficiency. This study assessed if OM applications increases soil or mineral fertilizer P availability to rice under anaerobic (flooded) condition and if that effect is different relative to that in aerobic (nonflooded) soils. Rice was grown in P‐deficient soil treated with combinations of addition of mineral P (0, 26 mg P/kg), OM (0, ~9 g OM/kg as rice straw + cattle manure) and water treatments (flooded vs nonflooded) in a factorial pot experiment. The OM was either freshly added just before flooding or incubated moist in soil for 6 months prior to flooding; blanket N and K was added in all treatments. Fresh addition of OM promoted reductive dissolution of Fe(III) minerals in flooded soils, whereas no such effect was found when OM had been incubated for 6 months before flooding. Yield and shoot P uptake largely increased with mineral P addition in all soils, whereas OM addition increased yield and P uptake only in flooded soils following fresh OM addition. The combination of mineral P and OM gave the largest yield and P uptake. Addition of OM just prior to soil flooding increased P uptake but was insufficient to overcome P deficiency in the absence of mineral P. Larger applications of OM are unlikely to be more successful in flooded soils due to side effects, such as Fe toxicity.