Methane emission from a wetland plant: the role of CH4 oxidation in Eriophorum

The importance of plant-mediated CH₄ transport was studied in a northern wetland. CH₄ transport through Eriophorum, a dominant sedge, was found to be the major pathway for CH₄ fluxes. Mean emission from Sphagnum lawns was low (34 g CH₄ m^-2 h^-1) and significantly higher from tussocks of Eriophorum vaginatum (974 g CH₄ m^-2 h^-1; U-test, p < 0.05). Mean flux from single tillers of Eriophorum angustifolium was 92 g CH₄ h^-1. In contrast to other ecosystems, no CH₄ oxidation was associated with Eriophorum. Hence, the lack of oxidation is one reason for the high emission rates from these ecosystems. This finding is a caveat for models of CH₄ emission and may also have consequences for carbon flow models of northern wetlands.     

Methane emissions from rice microcosms: The balance of production, accumulation and oxidation

In rice microcosms (Oryza sativa, var. Roma, type japonica),CH₄ emission, CH₄ production, CH₄oxidation and CH₄ accumulation were measured over an entirevegetation period. Diffusive CH₄ emission was measured inclosed chambers, CH₄ production was measured in soil samples,CH₄ oxidation was determined from the difference between oxicand anoxic emissions, and CH₄ accumulation was measured byanalysis of porewater and gas bubbles. The sum of diffusiveCH₄ emission, CH₄ oxidation, andCH₄ accumulation was only 60% of the cumulativeCH₄ production. The two values diverged during the first 50days (vegetative phase) and then again during the last 50 days (latereproductive phase and senescence) of the 150 day vegetation period. Duringthe period of day 50–100 (early reproductive phase/flowering), theprocesses were balanced. Most likely, gas bubbles and diffusion limitationare responsible for the divergence in the early and late phases. The effectof rice on CH₄ production rates and CH₄concentrations was studied by measuring these processes also in unplantedmicrocosms. Presence of rice plants lowered the CH₄concentrations, but had no net effect on the CH₄ productionrates.     

Effects of ammonium-based fertilisation on microbialprocesses involved in methane emission from soilsplanted with rice

The emission of the greenhouse gas CH₄ from ricepaddies is strongly influenced by management practicessuch as the input of ammonium-based fertilisers. Weassessed the impact of different levels (200 and 400kgN.ha^–1) of urea and (NH₄)₂HPO₄on the microbial processes involved in production andconsumption of CH₄ in rice field soil. We usedcompartmented microcosms which received fertilisertwice weekly. Potential CH₄ production rates weresubstantially higher in the rice rhizosphere than inunrooted soil, but were not affected by fertilisation.However, CH₄ emission was reduced by the additionof fertiliser and was negatively correlated with porewater NH ₄ ^plus concentration, probably as theconsequence of elevated CH₄ oxidation due tofertilisation. CH₄ oxidation as well as numbersof methanotrophs was distinctly stimulated by theaddition of fertiliser and by the presence of the riceplant. Without fertiliser addition,nitrogen-limitation of the methanotrophs will restrictthe consumption of CH₄. This may have a majorimpact on the global CH₄ budget, asnitrogen-limiting conditions will be the normalsituation in the rice rhizosphere. Elevated potentialnitrifying activities and numbers were only detectedin microcosms fertilised with urea. However, asubstantial part of the nitrification potential in therhizosphere of rice was attributed to the activity ofmethanotrophs, as was demonstrated using theinhibitors CH₃F and C₂H₂.     

Methane production and methane consumption: a review of processes underlying wetland methane fluxes

Potential rates of both methane production and methane consumptionvary over three orders of magnitude and their distribution is skew.These rates are weakly correlated with ecosystem type, incubationtemperature, in situ aeration, latitude, depth and distanceto oxic/anoxic interface. Anaerobic carbon mineralisation is amajor control of methane production. The large range in anaerobicCH₄:CO₂ production rates indicate that a largepart of the anaerobically mineralised carbon is used for reduction ofelectron acceptors, and, hence, is not available for methanogenesis.Consequently, cycling of electron acceptors needs to be studied tounderstand methane production. Methane and oxygen half saturationconstants for methane oxidation vary about one order of magnitude.Potential methane oxidation seems to be correlated withmethanotrophic biomass. Therefore, variation in potential methaneoxidation could be related to site characteristics with a model ofmethanotrophic biomass.     

Processes involved in formation and emission of methane in rice paddies

The seasonal change of the rates of production and emission of methane were determined under in-situ conditions in an Italian rice paddy in 1985 and 1986. The contribution to total emission of CH₄ of plant-mediated transport, ebullition, and diffusion through the flooding water was quantified by cutting the plants and by trapping emerging gas bubbles with funnels. Both production and emission of CH₄ increased during the season and reached a maximum in August. However, the numbers of methanogenic bacteria did not change. As the rice plants grew and the contribution of plant-mediated CH₄ emission increased, the percentage of the produced CH₄ which was reoxidized and thus, was not emitted, also increased. At its maximum, about 300 ml CH₄ were produced per m² per hour. However, only about 6% were emitted and this was by about 96% via plant-mediated transport. Radiotracer experiments showed that CH, was produced from H₂/CO₂. (30–50%) and from acetate. The pool concentration of acetate was in the range of 6–10 mM. The turnover time of acetate was 12–16 h. Part of the acetate pool appeared to be not available for production of CH₄ or CO₂     

美国俄亥俄州人工河滨湿地甲烷排放

2008年11月-2009年10月,在美国俄亥俄州哥伦布市Olentangy河河滨湿地,运用静态箱·气相色谱法对比研究了不同水文模式和植被生长状况下2种植被类型(人工植被和自然植被)淡水河滨恢复湿地甲烷(CH4)排放的时空规律,探讨了湿地土壤温度、水文条件、植被和土壤碳含量等因子对CH4排放的影响.结果表明,人工植被和自然植被湿地CH4排放通量均有明显的季节变化规律,但自然植被的淡水湿地CH4排放量仍明显高于人工植被湿地的排放量,其年排放量分别为68和114gCH4-C· m-2·a-1(P＜0.05),这是由于自然植被湿地相对于人工植被湿地有着更高的累积生产力.在2个实验湿地中,淹没深水区比干湿交替区有更高的CH4排放量,CH4排放通量的中值(平均值)分别为4.7(59.9)和0.09( 1.17)mg·m-2·h-1(P＜0.01),波动的水文相对于静止水文条件可减少CH4排放量.并且,实验湿地CH4排放通量与土壤温度和土壤有机碳含量有一定的相关性.因此,可通过对湿地进行适当的植物配置和水文条件等设计和管理措施有效地减少CH4排放.     

Methane and nitrous oxide emissions from rice paddy fields as affected by nitrogen fertilisers and water management

Methane and N₂O emissions affected by nitrogen fertilisers were measured simultaneously in rice paddy fields under intermittent irrigation in 1994. Ammonium sulphate and urea were applied at rates of 0 (control), 100 and 300 kg N ha^-1. The results showed that CH₄ emission, on the average, decreased by 42 and 60% in the ammonium sulphate treatments and 7 and 14% in the urea treatments at rates of 100 and 300 kg N ha^-1, respectively, compared to the control. N₂O emission increased significantly with the increase in the nitrogen application rate. N₂O emission was higher from ammonium sulphate treatments than from the urea treatments at the same application rate. A trade-off effect between CH₄ and N₂O emission was clearly observed. The N₂O flux was very small when the rice paddy plots were flooded, but peaked at the beginning of the disappearance of floodwater. In contrast, the CH₄ flux peaked during flooding and was significantly depressed by mid-season aeration (MSA). The results suggest that it is important to evaluate the integrative effects of water management and fertiliser application for mitigating greenhouse gas emissions in order to attenuate the greenhouse effect contributed by rice paddy fields.     

Role of rice in mediating methane emission

Methane emitted at different plant conditions through the different organs of rice plants was studied using a closed chamber technique under the laboratory, phytotron, and greenhouse conditions in order to clarify and quantify the role of different organs of rice plant as methane emission sites. Rice plants grown in flooded soils emit methane to the atmosphere via the aerenchyma of leaves, nodes and panicles. Emission through the rice plants is controlled by diffusion. No methane is emitted via the transpiration stream. Leaves are the major release sites at the early growth stage while nodes become more important later. Cracks and porous structure were found in the nodes. Panicles generally contribute little to methane emission. Increasing water depth temporarily reduces methane emission while concentration gradients in rice plants readjust to unsubmerged emission sites. Methane emissions in rice plants cease only when the plants become totally submerged.     

Methane emission from Arctic tundra

Concerns about a possible feedback effect on global warming following possible increased emissions of methane from tundra environments have lead to series of methane flux studies of northern wetland/tundra environments. Most of these studies have been carried out in boreal sub-Arctic regions using different techniques and means of assessing representativeness of the tundra. Here are reported a time series of CH₄ flux measurements from a true Arctic tundra site. A total of 528 independent observations were made at 22 fixed sites during the summers of 1991 and 1992. The data are fully comparable to the most extensive dataset yet produced on methane emissions from sub-Arctic tundra-like environments. Based on the data presented, from a thaw-season with approximately 55% of normal precipitation, a global tundra CH₄ source of 18–30 Tg CH₄ yr⁻¹ is estimated. This is within the range of 42±26 Tg CH₄ yr⁻¹ found in a similar sub-Arctic tundra environment. No single-parameter relationship between one environmental factor and CH₄ flux covering all sites was found. This is also in line with conclusions drawn in the sub-Arctic. However, inter-season variations in CH₄ flux at dry sites were largely controlled by the position of the water table, while flux from wetter sites seemed mainly to be controlled by soil temperature.     

Impact of gas transport through rice cultivars on methane emission from rice paddy fields

Two Italian rice (Oryza sativa var. japonica) cultivars, Lido and Roma, were tested in the field for methane production, oxidation and emission. In two consecutive years, fields planted with the rice cultivar Lido showed methane emissions 24–31% lower than fields planted with the cultivar Roma. This difference was observed irrespective of fertilizer treatment. In contrast to methane emissions, differences in methane production or oxidation were not observed between fields planted with the two cultivars. Plant-mediated transport of methane from the sediment to the atmosphere was the dominating pathway of methane emission. During the entire vegetation period, the contribution of this pathway to total methane emission amounted to c. 90%, whereas the contribution of gas bubble release and of diffusion through the water column to total methane emission was of minor significance. Results obtained from transport studies of tracer gas through the aerenchyma system of rice plants demonstrated that the root–shoot transition zone is the main site of resistance to plant-mediated gas exchange between the soil and the atmosphere. The cultivar Lido, showing relatively low methane emissions in the field, had a significantly lower gas transport capacity through the aerenchyma system than the cultivar Roma. Thus, the observed differences in methane emissions in the field between the cultivars Lido and Roma can be explained by different gas transport capacities. Apparently, these differences in gas transport capacities are a consequence of differences in morphology of the aerenchyma systems, especially in the root–shoot transition zone. It is, therefore, concluded that identification and use of high-yielding rice cultivars which have a low gas transport capacity represent an economically feasible, environmentally sound and promising approach to mitigating methane emissons from rice paddy fields.     

Quantification of methane emissions from Chinese rice fields (Zhejiang Province) as influenced by fertilizer treatment

Methane emissions from rice paddies were quantified by using an automatic field system stationed in Zhejiang Province, one of the centres for rice cultivation in China. The data set showed pronouned interannual variations over 5 consecutive vegetation periods; by computing average values of all experimental plots the annual emissions were 177 g CH₄ m⁻² yr⁻¹ in 1987, 50 g CH₄ m⁻² yr⁻¹ in 1988, and 187 g CH₄ m⁻² yr⁻¹ in 1989. The field preparations encompassed 4 different treatments: (1) no fertilizers, (2) mineral fertilizer (KCl, K₂SO₄), (3) organic manure (rape seeed cake, animal manure), (4) mineral fertilizer plus organic manure. The methane emission rates of the different fertilizer treatments did not show significant differences. The mean emission rates, calculated over the entire observation period of 5 seasons, were 30.4 mg CH₄ m⁻² h⁻¹ (non-fertilized plot) and 28.3 mg CH₄ m⁻² h⁻¹ (mineral fertilizers). These values indicate a high level of methane production even without additional input of organic material into the rice-soils. In the other plots, the organic fertilizers were added once per vegetation period at app. 1 t fresh weight per ha, a relatively low application rate by agronomical standards. The mean emission rates were 35.1 mg CH₄ m⁻² h⁻¹ when manure was applied as sole fertilizer and 27.5 mg CH₄ m⁻² h⁻¹ when applied jointly with potassium fertilizers. Based on the results of this study we estimate a range of 18–28 Tg CH₄ yr⁻¹ as the total methane emission from Chinese rice fields. However, more field data from representative sites in China are needed to reduce the uncertainties in this estimate.     

Microbial processes influencing methane emission from rice fields

Irrigated rice fields are an important source of atmospheric methane. In order to improve our understanding of the controlling processes, we measured in situ CH₄ emission and CH₄ oxidation in an Italian rice field in 1998 and 1999, and studied CH₄ production in soil and root samples. The CH₄ emission rates were correlated with diurnal temperature variations and showed pronounced seasonal and interannual variations. The contribution of CH₄ oxidation to total CH₄ flux, determined by specific inhibition with difluoromethane, decreased from 40% at the beginning to zero at the end of the season. The stable carbon isotopic composition of the emitted CH₄ also decreased. The CH₄‐oxidizing bacteria probably became limited by nitrogen as indicated by the seasonal decrease of NH₄⁺. Thus, CH₄ oxidation had little effect on CH₄ emission. Methane production on rice roots was relatively constant over the season. Methane production in soil slowly increased after flooding and was highest in the middle of the season. Pore water concentrations of CH₄ showed a similar seasonal pattern. In 1999, CH₄ production increased later in the season and reached lower rates than in 1998. An additional drainage in 1999 resulted in higher ferric iron concentrations, higher soil redox potentials and lower acetate concentrations. As a result, acetate‐utilizing methanogens were probably out‐competed by iron‐reducers so that a larger percentage of [2–¹⁴C]acetate was converted to ¹⁴CO₂ instead of ¹⁴CH₄. The residual CH₄ production was relatively low and was mainly due to H₂/CO₂‐dependent methanogenesis. Experiments with radioactive bicarbonate and with methyl fluoride as specific inhibitor showed that the theoretical ratio of 7:3 of methanogenesis from acetate vs. H₂/CO₂ was only reached later in the season when total CH₄ production was at the maximum. In conclusion, our results give a mechanistic explanation for the intraseasonal and interannual differences in CH₄ emission.     

Methane production capacities of different rice soils derived from inherent and exogenous substrates

Methane production rates were determined at weekly intervals during anaerobic incubation of eleven Philippine rice soils. The average production rates at 25 °C varied in a large range from 0.03 to 13.6 g CH_{4 g(d.w. soil)} ^-1d^-1. The development of methane production rates derived from inherent substrate allowed a grouping of soils in three classes: those with instantaneous development, those with a delay of approximately two weeks, and those with a suppression of methane production of more than eight weeks. Incubation at 30 and 35 °C increased production capacities of all soils, but the grouping of soils was still maintained. The Arrhenius equation provided a good fit for temperature effects on methane production capacities except for those soils with suppressed production. Acetate amendment strongly enhanced methane production rates and disintegrated the grouping. However, the efficiencies in converting acetate to methane differed among soils. Depending on the soil, 16.5–66.7% of the added acetate was utilized within five weeks incubation at 25 °C.Correlation analyses of methane production (over eight weeks) and physico-chemical soil parameters yielded significant correlations for the concentrations of organic carbon (R² = 0.42) and organic nitrogen (R² = 0.52). Correlation indices could substantially be enhanced by using the enriched fraction of organic carbon (R² = 0.94) and organic nitrogen (R² = 0.77), i.e. the differential between topsoil and subsoil concentrations of the respective compounds. The enriched organic material in the topsoil corresponds to the biologically active fraction and thus represents a good indicator of methane production derived from inherent substrate. The best indicators of the conversion rate of acetate in different soils were pH-value (R² = 0.56) and organic carbon content (R² = 0.52).Apparently, soil properties affect methane production through various pathways. Inherent organic substrate represents a considerable source of methane in some soils and is negligible in others. Likewise, soils also differ regarding the response to exogenous substrate. Both mechanisms yield in a distinct spatial variability of methane production in rice soils.     

Methane consumption in two temperate forest soils

Forest soils are thought to be an important sink for atmospheric methane. To evaluate methane consumption,¹⁴C-labeled methane was added to the headspace of intact soil cores collected from a mixed mesophytic forest and from a red spruce forest located in the central Appalachian Mountains. Both soils consumed the added methane at initially high rates that decreased as the methane mixing ratio of the air decreased. The mixed mesophytic forest soil consumed an average of 2 mg CH₄ m^–2 d^–1 versus 1 mg CH, m^–2 d^–1 for the spruce forest soil. The addition of acetylene to the headspace completely suppressed methane consumption by the soils, suggesting that an aerobic methane-consuming microorganism mediated the process. At both forest sites, methane mixing ratios in soil air spaces were greater than that in the air overlying the soil surface, indicating that these soils had the ability to produce methane. Models of methane emission from forest soils to the atmosphere must represent methane flux as the balance between production and consumption of methane, which are controlled by very different factors     

Bacterial Processes of the Methane Cycle in Bottom Sediments of Lake Baikal

The activity of methanogenic and methanotrophic bacteria was evaluated in bottom sediments of Lake Baikal. Methane concentration in Baikal bottom sediments varied from 0.0053 to 81.7 ml/dm³. Bacterial methane was produced at rates of 0.0004–534.7 l CH₄/(dm³ day) and oxidized at rates of 0.005–1180 l CH₄/(dm³ day). Peak methane production and oxidation were observed in Frolikha Bay near a methane vent. Methane was emitted into water at rates of 49.2–4340 l CH₄/(m² day). Rates of bacterial methane oxidation in near-bottom water layers ranged from 0.002 to 1.78 l/(l day). Methanogens and methanotrophs were found to play an important role in the carbon cycle through all layers of sediments, particularly in the areas of methane vent and gas-hydrate occurrence.     

盐分对湿地甲烷排放影响的研究进展

当前在全球气候变化和人类活动双重作用下,湿地正在或者将要面临着显著的盐分变化形势,尤其是内陆和滨海咸化湿地。湿地是大气甲烷的重要排放源。甲烷排放是甲烷产生、氧化和传输过程综合作用的结果。盐分变化将影响湿地水-土环境,降低植物群落初级生产力和有机物积累速率,改变微生物主导的有机物矿化速率和途径等,进而改变湿地生态系统的结构和功能,影响湿地甲烷产生、氧化、传输和排放系列过程。本文综述了盐分(浓度与组成)对湿地甲烷产生与排放的影响结果,从底物供给、微生物(产甲烷菌和甲烷氧化菌等)数量、活性与群落组成、酶活性、植物、电子受体、p H和氧化还原电位等几个关键方面分析了盐分影响湿地甲烷排放过程的内在机制。在此基础上提出了今后需重点关注的5个方面:1)加强盐分浓度与组成对湿地甲烷产生、氧化、传输与排放影响的系统性、框架性研究;2)深入探讨盐分背景、变化幅度与速率的耦合如何影响湿地甲烷系列过程;3)不同离子组成及其交互效应如何影响湿地甲烷动态过程;4)结合生物学、基因组学及同位素技术等,加强湿地产甲烷菌与甲烷氧化菌与盐分的关系及其响应研究;5)湿地甲烷对盐分变化响应的时空分异规律。     

铁炉渣施加对稻田甲烷产生、氧化与排放的影响

为了阐明铁炉渣施加对稻田甲烷产生、氧化与排放的影响,采用静态箱-气相色谱法对对照(CK)、2 Mg/hm2(FeⅠ)、4Mg/hm2(FeⅡ)和8 Mg/hm2(FeⅢ)铁炉渣施加后稻田甲烷产生、氧化与排放进行了测定与分析.研究结果表明:观测期内,CK、Fe Ⅰ、FeⅡ和FeⅢ样地甲烷产生量分别为0.06-8.87、0.12-8.28、0.15-7.84、0.17-7.82 mg·m-2·h-1,平均产生量分别为4.68、3.92、3.14、2.76 mg·m-2·h-1;甲烷氧化量分别是0.02-1.27、0.09-0.95、0.09-1.54、0.09-2.79 mg·m-2·h-1,平均氧化量为0.46、0.47、0.59、0.55 mg·m-2·h-1;甲烷排放分别是0.04-7.99、0.03-7.33、0.06-6.30、0.08-5.12 mg· m-2·h-1,平均值分别为3.11、2.29、1.76、1.59 mg·m-2·h-1.铁炉渣的施加降低了甲烷产生量和排放通量,提高了甲烷氧化量.     

Influence of rice cultivar on methane emission from paddy fields

Influence of rice cultivars on CH₄ emissions from a paddy field was studied using four Japonica types, two Indica types, and two Japonica/Indica F₁ hybrids. In addition, the suppression of CH₄ emission by interrupting irrigation at the flowering stage was investigated. Patterns of seasonal variation in CH₄ emission rates were similar among the eight cultivars. Two of the Japonica types showed the maximum and minimum CH₄ emissions among the cultivars investigated. Neither the number of tillers, shoot length, shoot weight, and root weight correlated with the CH₄ emission rates at the tillering and reproductive growth stages. Following temporary interruption of irrigation at the flowering stage, CH₄ emission rates decreased drastically and remained at very low levels until the harvesting stage, indicating its great effectiveness for the suppression of CH₄ emission from rice paddies.     

稻田甲烷排放模型研究——模型的验证

模型的有效性检验是模型应用于估计区域尺度稻田甲烷排放量的基本前提 ,尤其是针对多种不同的土壤、气候以及农业管理方式等可能影响稻田甲烷排放的环境条件下的模型检验。利用覆盖全国主要水稻产区的 94个甲烷排放观测案例对稻田甲烷排放模型 (CH4 MOD)进行了验证。这些观测区域分布范围北至北京 (4 0°30′N,116°2 5′E) ,南至广州 (2 3°0 8′N,113°2 0′E) ,东起杭州 (30°19′N,12 0°12′E) ,西到四川的土主 (2 9°4 0′N,10 3°5 0′E)。既有双季稻 ,也有单季稻 ,稻田灌溉及施肥方式也多种多样 ,对我国水稻生产具有较广泛的代表性。观测获得的稻田甲烷排放季节总量从 3.1kg C/hm2到 76 1.7kg C/hm2 ,平均值为199.4 (± 187.3) kg C/hm2 ;相应的模拟值分别为 13.9、82 4 .3和 2 2 4 .6 (± 187.0 ) kg C/hm2。模拟值与实测值的线性相关系数(r2 )为 0 .84 (n=94 ,p<0 .0 0 1)。CH4 MOD模型能够通过较少的输入参数有效地模拟我国主要农作方式下的稻田甲烷排放     

A semi-empirical model of methane emission from flooded rice paddy soils

Reliable regional or global estimates of methane emissions from flooded rice paddy soils depend on an examination of methodologies by which the current high variability in the estimates might be reduced. One potential way to do this is the development of predictive models. With an understanding of the processes of methane production, oxidation and emission, a semi-empirical model, focused on the contributions of rice plants to the processes and also the influence of environmental factors, was developed to predict methane emission from flooded rice fields. A simplified version of the model was also derived to predict methane emission in a more practical manner. In this study, it was hypothesized that methanogenic substrates are primarily derived from rice plants and added organic matter. Rates of methane production in flooded rice soils are determined by the availability of methanogenic substrates and the influence of environmental factors. Rice growth and development control the fraction of methane emitted. The amount of methane transported from the soil to the atmosphere is determined by the rates of production and the emitted fraction. Model validation against observations from single rice growing seasons in Texas, USA demonstrated that the seasonal variation of methane emission is regulated by rice growth and development. A further validation of the model against measurements from irrigated rice paddy soils in various regions of the world, including Italy, China, Indonesia, Philippines and the United States, suggests that methane emission can be predicted from rice net productivity, cultivar character, soil texture and temperature, and organic matter amendments.