Methane flux from mangrove sediments along the Southwestern coast of Puerto Rico

Although the sediments of coastal marine mangrove forests have been considered a minor source of atmospheric methane, these estimates have been based on sparse data from similar areas. We have gathered evidence that shows that external nutrient and freshwater loading in mangrove sediments may have a significant effect on methane flux. Experiments were performed to examine methane fluxes from anaerobic sediments in a mangrove forest subjected to secondary sewage effluents on the southwestern coast of Puerto Rico. Emission rates were measured in situ using a static chamber technique, and subsequent laboratory analysis of samples was by gas chromatography using a flame ionization detector. Results indicate that methane flux rates were lowest at the landward fringe nearest to the effluent discharge, higher in the seaward fringe occupied by red mangroves, and highest in the transition zone between black and red mangrove communities, with average values of 4 mg CH₄ m^?2 d^?1, 42 mg CH₄ m^?2 d^?1, and 82 mg CH₄ m^?2 d^?1, respectively. Overall mean values show these sediments may emit as much as 40 times more methane than unimpacted pristine areas. Pneumatophores ofAviciennia germinans have been found to serve as conduits to the atmosphere for this gas. Fluctuating water level overlying the mangrove sediment is an important environmental factor controlling seasonal and interannual CH₄ flux variations. Environmental controls such as freshwater inputs and increased nutrient loading influence in situ methane emissions from these environments.     

Gas flux to the atmosphere from mud volcanoes in eastern Romania

Gas flux measurements have for the first time been taken from vents and soil of eastern Romania mud volcanoes, the largest geological structures in Europe releasing methane into the atmosphere. In the quiescent phase, the methane emission from single vents is up to 28 t yr^?1. Diffuse soil microseepage is of the order of 10²?10⁵ mg m^?2 day^?1. A total output of at least 1200 tonnes of CH₄ per year can be conservatively estimated over the area investigated alone (～ 2.3 km²). Helium fluxes are up to five orders of magnitude higher than the average flux in a stable continental area, pointing to a close link between mud volcanoes and crustal degassing through faults crossing the deep hydrocarbon reservoirs. These data represent a key contribution towards refining global CH₄‐emission estimates, which indicate mud volcanoes as a significant and unavoidable source of greenhouse gases for the atmosphere.     

Methane formation in soil–plant systems treating wastewater as influenced by microbial populations

The present study evaluated the effect of plant species on methane (CH₄) emission and microbial populations in three types of soil–plant systems. Results showed large variation of CH₄ flux rate ranging from 1.35 to 212.61 mg CH₄ m^?2 h^?1. Emission peak of CH₄ occurred in July. No significant difference was found in the non-vegetation system spanning 2 years. Compared with non-vegetation, vegetation systems had much higher flux of CH₄, and obvious seasonal variation was observed. The polyculture system planted with Zizania latifolia (Z. latifolia) and Phragmites australis (P. australis) released higher CH₄ fluxes than the mono system (P. australis), reflecting that Z. latifolia growth could simulate CH₄ emission. The fluorescence in situ hybridization (FISH) results support the characteristics of CH₄ fluxes. Much higher methanotrophs amount and lower methanogens amount from the mono system than those from the polyculture system was observed indicating that Z. latifolia growth may limit the oxygen transportation resulting in higher CH₄ emission. The polyculture system has the highest potential of CH₄ emission.     

Measuring daytime CO2 fluxes from the inter-tidal mangrove soils of Indian Sundarbans

The aim of this research was to measure the rate of carbon dioxide (CO₂) exchange between the soil and atmosphere in the inter-tidal forest floor of the Indian Sundarbans mangrove ecosystem and to study its response with soil temperature and soil water content. Soil CO₂ effluxes were monitored every month at two stations (between April, 2011 and March, 2012); one situated at the land–ocean boundary of the Bay of Bengal (outer part of the mangrove forest) and the other lying 55 km inshore from the coast line (inner part of the mangrove forest). The static closed chamber technique was implemented at three inter-tidal positions (landward, seaward and bare mudflats) in each station. Fluxes were measured in the daytime every half an hour by circulating chamber headspace air through a sampling manifold assembly and a closed-path non-dispersive infrared gas analyser. The fluxes ranged between 0.15 and 2.34 μmol m^?2 s^?1 during the annual course of sampling. Effluxes of higher magnitude were measured during summer; however, it abruptly decreased during the monsoon. CO₂ flux from the forest floor was strongly related to soil temperature, with the highest correlation found with temperature at 2 cm depth. No such significant relationship between soil water content and CO₂ efflux could be properly ascertained; however, excessively high soil water content was found to be the only reason which hampered the rate of effluxes during the monsoon. On the whole, landward (LW) sites of the mangrove forest emitted more than the seaward (SW) sites. Q ₁₀ values (obtained from simple exponential model) which denote the multiplicative factor by which the efflux rate increases for a 10 °C rise in temperature ranged between 2.07 and 4.05.     

Variability in Concentrations and Fluxes of Methane in the Indian Estuaries

In order to examine the fluxes of methane (CH₄) from the Indian estuaries, measurements were carried out by collecting samples from 26 estuaries along the Indian coast during high discharge (wet) and low water discharge (dry) periods. The CH₄ concentrations in the estuaries located along the west coast of India were significantly higher (113?±?40 nM) compared to the east coast of India (27?±?6 nM) during wet and dry periods (88?±?15 and 63?±?12 nM, respectively). Supersaturation of CH₄ was observed in the Indian estuaries during both periods ((0.18 to 22.3?×?10³ %). The concentrations of CH₄ showed inverse relation with salinity indicating that freshwater is a significant source. Spatial variations in CH₄ saturation were associated with the organic matter load suggesting that its decomposition may be another source in the Indian estuaries. Fluxes of CH₄ ranged from 0.01 to 298 μmol m^?2 day^?1 (mean 13.4?±?5 μmol m^?2 day^?1) which is ~30 times lower compared to European estuaries (414 μmol m^?2 day^?1). The annual emission from Indian estuaries, including Pulicat and Adyar, amounted to 0.39?×?10¹⁰ g CH₄?year^?1 with the surface area of 0.027?×?10⁶ km² which is significantly lower than that in European estuaries (2.7?±?6.8?×?10¹⁰ g CH₄?year^?1 with the surface area of 0.03?×?10⁶ km²). This study suggests that Indian estuaries are a weak source for atmospheric CH₄ than European estuaries and such low fluxes were attributed to low residence time of water and low decomposition of organic matter within the estuary. The CH₄ fluxes from the Indian estuaries are higher than those from Indian mangroves (0.01?×?10¹⁰ g CH₄?year^?1) but lower than those from Indian inland waters (210?×?10¹⁰ g CH₄?year^?1).     

Quantification of methane emission from bacterial mat sites at Quepos Slide offshore Costa Rica

Seafloor methane emission from the Quepos Slide on the submarine segment of the Costa Rica fore-arc margin was estimated by extrapolating flux measurements from individual seeps to the total area covered by bacterial mats. This approach is based on the combination of detailed mapping to determine the abundance of seeps and the application of a numerical model to estimate the amount of benthic methane fluxes. Model results suggest that the majority of the studied seeps transport rather limited amount of methane (on average: ~177 μmol cm^?2 a^?1) into the water column due to moderate upward advection, allowing for intense anaerobic oxidation of methane (AOM; on average: 53 % of the methane flux is consumed). Depth-integrated AOM rates (56–1,538 μmol CH₄ cm^?2 a^?1) are comparable with values reported from other active seep sites. The overall amount of dissolved methane released into the water column from the entire area covered by bacterial mats on the Quepos Slide is estimated to be about 0.28 × 10⁶ mol a^?1. This conservative estimate which relies on rather accurate determinations of seafloor methane fluxes emphasizes the potential importance of submarine slides as sites of natural methane seepage; however, at present the global extent of methane seepage from submarine slides is largely unknown.     

Methane and carbon dioxide flux from a macrotidal salt marsh,Bay of Fundy,New Brunswick

Fluxes of methane (CH₄) and carbon dioxide (CO₂) to the atmosphere at 52 sites within a salt marsh were measured by a dark static chamber technique from mid July to mid September. Mean CH₄ fluxes ranged from 0.2 mg m^?2 d^?1 to 11.0 mg m^?2 d^?1, with an overall average of 1.6 mg m^?2 d^?1. Flux of CH₄ was inversely correlated (r²=0.23, p = 0.001) with salinity of the upper porewater at the site, suggesting the dominant role of SO₄ ^2? in inhibiting methanogenesis in salt-marsh sediments. The combination of salinity and water table position was able to explain only 29% of the variance in CH₄ emission. Mean soil flux of CO₂ ranged from 0.3 g m^?2 d^?1 to 3.7 g m^?2 d^?1, with an overall average of 2.5 g m^?2 d^?1; it was correlated with aboveground biomass (positive, r²=0.38, p = 0.001) and position of the water table (negative, r² = 0.55, p = 0.001). The combination of biomass and water table position accounted for 63% of the variance in CO₂ flux. There were high variations in gas flux within the six plant communities. The sequences were CH₄: upland edge > panne > pool > middle marsh > low marsh > high marsh, and CO₂: middle marsh > low marsh > upland edge > high marsh > panne > pool. Compared to other salt-marsh systems, this Bay of Fundy marsh emits small amounts of CH₄ and CO₂.     

神农架大九湖泥炭湿地甲烷通量特征及其与土壤微生物群落组成的关系

虽然神农架大九湖泥炭湿地的甲烷排放特征、土壤微生物群落组成已有一些研究,但是关于微生物群落与甲烷排放量的关系及影响的研究不多.采用涡度相关法和高通量测序技术,探讨2016年3月~2017年2月微生物对大九湖泥炭湿地CH₄通量排放的影响.结果表明,大九湖泥炭湿地研究期间表现为CH₄的源,年总排放量5 566.27 mg·m-2,日平均排放速率10.96 nmol·m-2·s-1;春、夏、秋、冬四季的平均通量分别为12.06、22.47、3.02、2.92 nmol·m-2·s-1;研究区优势菌为泉古菌（54.6%）、广古菌（18.9%）、酸杆菌（12.6%）等.对不同季节样品Shannon指数进行单因素分析,p值为0.000 127,分析结果表明:CH₄月通量变化均呈明显的倒“U”型;夏季CH₄通量最高,冬季最低;不同季节的微生物群落物种多样性存在显著差异;夏季、冬季微生物群落组成与CH₄通量分别呈显著正相关、显著负相关;未鉴别出的菌群和俭菌总门与CH₄通量呈极显著正相关关系,泉古菌门与CH₄通量呈极显著负相关关系.      

Benthic Oxygen Fluxes Measured by Eddy Covariance in Permeable Gulf of Mexico Shallow-Water Sands

Oxygen fluxes across the sediment–water interface reflect primary production and organic matter degradation in coastal sediments and thus provide data that can be used for assessing ecosystem function, carbon cycling and the response to coastal eutrophication. In this study, the aquatic eddy covariance technique was used to measure seafloor–water column oxygen fluxes at shallow coastal sites with highly permeable sandy sediment in the northeastern Gulf of Mexico for which oxygen flux data currently are lacking. Oxygen fluxes at wave-exposed Gulf sites were compared to those at protected Bay sites over a period of 4 years and covering the four seasons. A total of 17 daytime and 14 nighttime deployments, producing 408 flux measurements (14.5 min each), were conducted. Average annual oxygen release and uptake (mean ± standard error) were 191 ± 66 and ?191 ± 45 mmol m^?2 day^?1 for the Gulf sites and 130 ± 57 and ?152 ± 64 mmol m^?2 day^?1 for the Bay sites. Seasonal variation in oxygen flux was observed, with high rates typically occurring during spring and lower rates during summer. The ratio of average oxygen release to uptake at both sites was close to 1 (Bay: 0.9, Gulf: 1.0). Close responses of the flux to changes in light, temperature, bottom current velocity, and wave action (significant wave height) documented tight physical–biological, benthic–pelagic coupling. The increase of the sedimentary oxygen uptake with increasing temperature corresponded to a Q₁₀ temperature coefficient of 1.4 ± 0.3. An increase in flow velocity resulted in increased oxygen uptake (by a factor of 1–6 for a doubling in flow), which is explained by the enhanced transport of organic matter and electron acceptors into the permeable sediment. Benthic photosynthetic production and oxygen release from the sediment was modulated by light intensity at the temporal scale (minutes) of the flux measurements. The fluxes measured in this study contribute to baseline data in a region with rapid coastal development and can be used in large-scale assessments and estimates of carbon transformations.     

基于涡度相关技术估算植被/大气间净CO2交换量中的不确定性

近年来，涡度相关技术的进步使陆地生态系统CO2通量的长期和连续观测成为可能。目前，涡度相关技术是全球通量观测网络（FLUXNET）测定植被/大气间CO2通量的主要技术手段，但绝大部分CO2通量观测站点都处于非典型的理想条件下，不能完全满足涡度相关技术的基本假设条件，从而导致基于涡度相关技术估算植被/大气间净生态系统CO2交换量的不确定性。系统介绍了涡度相关技术的基本假设，基本理论公式和误差的类型与特征等理论问题，重点阐述了通量测定中仪器本身的物理限制、二维和三维的气流运动、数据处理的方法和夜间通量的低估等不确定性的主要来源，并据此对通量观测研究中需要优先考虑的问题提出一些建议。研究认为数据质量控制与分析以及误差评价是不同通量站点间的结果比较和全球尺度综合分析的过程中需重点考虑的问题。     

Methane distribution and cycling in Tomales Bay, California

Cycling of methane (CH₄) in Tomales Bay, a 28-km² temperature estuary in northern California with relatively low inputs of organic carbon, was studied over a 1-yr period. Water column CH₄ concentrations showed spatial and temporal variability (range=8–100 nM), and were supersaturated with respect to the atmosphere by a factor of 2–37. Rates of net water column CH₄ production-oxidation were determined by in situ experiments, and were not found to be significantly different from zero. Fluxes across the sediment-water interface, determined by direct measurement using benthic chambers, varied from ?0.1 μmol m^?2 d^?1 to +16 μmol m^?2 d^?1 (positive fluxes into water). Methane concentrations in the two perennial creeks feeding the bay varied annually (140–950 nM); these creeks were a significant CH₄ source to the bay during winter. In addition, mass-balance calculations indicate a significant additional inter CH₄ source, which is hypothesized to result from storm-related runoff from dairy farms adjacent to the bay. Systemwide CH₄ budgets of the 16-km² inner bay indicate benthic production (110 mol d^?1) and atmospheric evasion (110 mol d^?1) dominated during summer, while atmospheric evasion (160 mol d^?1) and runoff from dairy farms (90 mol d^?1) dominated during winter.     

Biogeochemical cycling in an organic-rich coastal marine basin 4. An organic carbon budget for sediments dominated by sulfate reduction and methanogenesis

In situ carbon flux measurements and calculated burial rates are utilized to construct an organic carbon budget for the upper meter of sediment at a single station in Cape Lookout Bight, a small marine basin located on the Outer Banks of North Carolina, U.S.A. (34°37′N, 76°33′W). Of 149 ± 20 mole · m^?2 · yr^?1 of total organic carbon deposited, 35.6 ± 5.2 mole · m^?2 · yr^?1 is recycled to overlying waters, 84 ± 18% as ∑CO₂ and 16 ± 8% as CH₄. Approximately 68 ± 20% of the upward carbon flux is supported by sulfate reduction while 32 ± 16% takes place as the result of underlying methanogenesis. Measured ∑CO₂ and CH₄ sediment-water fluxes range seasonally from 1900–6300 and 50–2500 μmole · m^?2 · hr^?1 respectively.The mean residence time of metabolizable organic carbon in the upper 80 cm of sediment is approximately four months with greater than 98% of the calculated total remineralization taking place within three years. In spite of large upward fluxes of methane, larger molecules derived from metabolizable sedimentary organic carbon appear to be the dominant reductants for dissolved sulfate.     

Diurnal Variations of Carbon Dioxide, Methane, and Nitrous Oxide Vertical Fluxes in a Subtropical Estuarine Marsh on Neap and Spring Tide Days

Measuring fluxes of greenhouse gases (GHGs) is fundamental to estimating their impact on global warming. We examined diurnal variations of carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O) vertical fluxes in a tidal marsh ecosystem. Measurements were recorded on neap and spring tide days in April and September 2010 in the Shanyutan wetland of the Min River estuary, southeast China. Here, we define a positive flux as directing into the atmosphere. CH₄ fluxes on the diurnal scale were positive throughout, and CH₄ emissions into the atmosphere on neap tide days were higher than on spring tide days. CH₄ releases from the marsh ecosystem on neap tide days were higher in the daytime; however, on spring tide days, daily variations of CH₄ emissions were more complex. The marsh ecosystem plays a twofold role in both releasing and assimilating CO₂ and N₂O gases on the diurnal scale. Average CO₂ fluxes were positive on the daily scale both on neap and spring days and were greater on the neap tide days than on spring tide days. Diurnal variations of N₂O fluxes fluctuated more. Over the diurnal period, soil temperature markedly controlled variations of CH₄ emissions compared to other soil factors, such as salinity and redox potential. Tidal water height was a key factor influencing GHGs fluxes at the water–air interface. Compared with N₂O, the diurnal course of CO₂ and CH₄ fluxes in the marsh ecosystem appeared to be directly controlled by marsh plants. These results have implications for sampling and scaling strategies for estimating GHGs fluxes in tidal marsh ecosystems.     

Spatial and temporal distribution of methane in an extensive shallow estuary, South India

Sedimentary methane (CH₄) fluxes and oxidation rates were determined over the wet and dry seasons (four measurement campaigns) in Pulicat lake, an extensive shallow estuary in south India. Dissolved CH₄ concentrations were measured at 52 locations in December 2000. The annual mean net CH₄ flux from Pulicat lake sediments was 3.7 × 10⁹ g yr^-1 based on static chamber measurements. A further 1.7 × 10⁹g yr_-1 was estimated to be oxidized at the sediment-water interface. The mean dissolved concentration of CH₄ was 242nmol |^-1 (ranging between 94 and 501 nmol |^-1) and the spatial distribution could be explained by tidal dynamics and freshwater input. Sea-air exchange estimates using models, account only for ∼13% (0.5 × 10⁹ g yr-1) of the total CH₄ produced in sediments, whereas ebullition appeared to be the major route for loss to the atmosphere (∼ 63% of the net sediment flux). We estimated the total atmospheric source of CH₄ from Pulicat lake to be 0.5 to 4.0 × 10⁹g yr^-1.     

Modelling the effects of climate change on methane emission from a northern ombrotrophic bog in Canada

Peatlands are a large potential source of methane (CH₄) to the atmosphere. In order to investigate the effects of climate change on CH₄ emission from northern ombrotrophic peatlands, a simulation model coupling water table dynamics with methane emission was developed for the Mer Bleue Bog in Ontario, Canada. The model was validated against reported values of CH₄ flux from field measurements and the model outputs exhibited high sensitivity to acrotelm thickness, leaf area index, transmissivity and slope of water table. With a 2–4°C temperature rise over the 4-year simulation period, the rate of CH₄ release dropped significantly to under 0.1 mg m⁻² day⁻¹. On the other hand, mean CH₄ emission increased by >26-fold when the increase in precipitation was >15%. When looking at the combined effects, the highest CH₄ release (13.3 mg m⁻² day⁻¹) was attained under the scenario of 2°C temperature rise and 25% precipitation increase. Results obtained in this study highlight the importance of avoiding more extreme climate change, which would otherwise lead to enhanced methane release from peatlands and further atmospheric warming through positive feedback.     

Energy and CO<Subscript>2</Subscript> exchanges and influencing factors in spring wheat ecosystem along the Heihe River,northwestern China

Spring wheat (Triticum aestivum Linn.) is an important crop for food security in the desert-oasis farmland in the middle reaches of the Heihe River in northwestern China. We measured fluxes using eddy covariance and meteorological parameters to explore the energy fluxes and the relationship between CO₂ flux and climate change in this region during the wheat growing seasons in 2013 and 2014. The energy balance closures were 70.5% and 72.7% in the 2013 and 2014 growing season, respectively. The wheat ecosystem had distinct seasonal and diurnal dynamics of CO₂ fluxes with U-shaped curves. The accumulated net ecosystemic CO₂ exchanges (NEE) were -111.6 and -142.2 g C/m² in 2013 and 2014 growing season, respectively. The ecosystem generally acted as a CO₂ sink during the growing season but became a CO₂ source after the wheat harvest. A correlation analysis indicated that night-time CO₂ fluxes were exponentially dependent on air temperature and soil temperature at a depth of 5 cm but were not correlated with soil-water content, water-vapour pressure, or vapour-pressure deficit. CO₂ flux was not correlated with the meteorological parameters during daytime. However, irrigation and precipitation, may complicate the response of CO₂ fluxes to other meteorological parameters.     

若尔盖高原沼泽湿地CH4排放研究

若尔盖高原沼泽湿地海拔 3400 m，面积 4038km²，是我国面积最大的高原沼泽湿地分布区。2001年 5～9月的非冰冻期，其主要沼泽类型木里苔草沼泽的CH₄排放通量范围是 0.51～ 8.20 m g/（m ²· h），平均值为 2.87 m g/（m ²· h）；乌拉苔草沼泽CH₄排放通量范围是 0.36～10.04 m g/（m ²· h），平均值为 4.51 m g/（m ²· h）。在空间分布上，不同沼泽类型之间CH₄排放通量具有一定的差异。在季节变化上，没有明显的排放高峰。根据代表性观测点的CH₄平均排放量、日数和沼泽总面积推算，非冰冻期若尔盖高原沼泽湿地CH₄的排放量为 0.052Tg/a。     

Carbon Dioxide and Methane Emissions from Mangrove-Associated Waters of the Andaman Islands,Bay of Bengal

We estimated CO₂ and CH₄ emissions from mangrove-associated waters of the Andaman Islands by sampling hourly over 24 h in two tidal mangrove creeks (Wright Myo; Kalighat) and during transects in contiguous shallow inshore waters, immediately following the northeast monsoons (dry season) and during the peak of the southwest monsoons (wet season) of 2005 and 2006. Tidal height correlated positively with dissolved O₂ and negatively with pCO₂, CH₄, total alkalinity (TAlk) and dissolved inorganic carbon (DIC), and pCO₂ and CH₄ were always highly supersaturated (330–1,627 % CO₂; 339–26,930 % CH₄). These data are consistent with a tidal pumping response to hydrostatic pressure change. There were no seasonal trends in dissolved CH₄ but pCO₂ was around twice as high during the 2005 wet season than at other times, in both the tidal surveys and the inshore transects. Fourfold higher turbidity during the wet season is consistent with elevated net benthic and/or water column heterotrophy via enhanced organic matter inputs from adjacent mangrove forest and/or the flushing of CO₂-enriched soil waters, which may explain these CO₂ data. TAlk/DIC relationships in the tidally pumped waters were most consistent with a diagenetic origin of CO₂ primarily via sulphate reduction, with additional inputs via aerobic respiration. A decrease with salinity for pCO₂, CH₄, TAlk and DIC during the inshore transects reflected offshore transport of tidally pumped waters. Estimated mean tidal creek emissions were ～23–173 mmol m^?2 day^?1 CO₂ and ～0.11–0.47 mmol m^?2 day^?1 CH₄. The CO₂ emissions are typical of mangrove-associated waters globally, while the CH₄ emissions fall at the low end of the published range. Scaling to the creek open water area (2,700 km²) gave total annual creek water emissions ～3.6–9.2?×?10¹⁰ mol CO₂ and 3.7–34?×?10⁷ mol CH₄. We estimated emissions from contiguous inshore waters at ～1.5?×?10¹¹ mol CO₂?year^?1 and 2.6?×?10⁸ mol CH₄?year^?1, giving total emissions of ～1.9?×?10¹¹ mol CO₂?year^?1 and ～3.0?×?10⁸ mol CH₄?year^?1 from a total area of mangrove-influenced water of ～3?×?10⁴ km². Evaluating such emissions in a range of mangrove environments is important to resolving the greenhouse gas balance of mangrove ecosystems globally. Future such studies should be integral to wider quantitative process studies of the mangrove carbon balance.     

神农架大九湖泥炭湿地CH4通量特征及其影响因子

开展大九湖湿地生态系统CH₄通量研究,对深入了解碳循环机制、科学经营以及准确评估湿地生态系统碳收支等方面具有重要意义.以湖北省神农架林区大九湖亚高山泥炭湿地为研究区域,采用涡度相关法对CH₄通量进行原位连续观测,分析了泥炭湿地CH₄通量变化特征及其影响因素.结果表明,大九湖泥炭湿地在2015年8月至2016年5月期间表现为CH₄的源,日通量均值为15.57 nmol·m-2·s-1.CH₄通量具有“夜间极大值”(2:00或22:00) 和“三峰模式”(6:00、12:00和22:00) 两种昼夜变化规律;CH₄通量具有明显季节变化规律,8月释放最多(36.46 nmol·m-2·s-1),3月释放最少(3.92 nmol·m-2·s-1).相关性分析表明,大九湖泥炭湿地CH₄通量受空气温度(T_a)、土壤温度(T_s)、土壤含水量(SWC)和摩擦风速(U*)的共同影响;不同时间尺度上,各影响因子与CH₄通量的相关性有所差异.曲线拟合得出,CH₄通量与T_a和T_s呈指数增长趋势,与SWC呈二次曲线关系.      

Gas seepage from Tokamachi mud volcanoes, onshore Niigata Basin (Japan): Origin, post-genetic alterations and CH4-CO2 fluxes

Methane and CO₂ emissions from the two most active mud volcanoes in central Japan, Murono and Kamou (Tokamachi City, Niigata Basin), were measured in from both craters or vents (macro-seepage) and invisible exhalation from the soil (mini- and microseepage). Molecular and isotopic compositions of the released gases were also determined. Gas is thermogenic (δ¹³C_CH4 from −32.9‰ to −36.2‰), likely associated with oil, and enrichments of ¹³C in CO₂ (δ¹³C_CO2 up to +28.3‰) and propane (δ¹³C_C3H8 up to −8.6‰) suggest subsurface petroleum biodegradation. Gas source and post-genetic alteration processes did not change from 2004 to 2010. Methane flux ranged within the orders of magnitude of 10¹-10⁴ g m⁻² d⁻¹ in macro-seeps, and up to 446 g m⁻² d⁻¹ from diffuse seepage. Positive CH₄ fluxes from dry soil were widespread throughout the investigated areas. Total CH₄ emission from Murono and Kamou were estimated to be at least 20 and 3.7 ton a⁻¹, respectively, of which more than half was from invisible seepage surrounding the mud volcano vents. At the macro-seeps, CO₂ fluxes were directly proportional to CH₄ fluxes, and the volumetric ratios between CH₄ flux and CO₂ flux were similar to the compositional CH₄/CO₂ volume ratio. Macro-seep flux data, in addition to those of other 13 mud volcanoes, supported the hypothesis that molecular fractionation (increase of the “Bernard ratio” C₁/(C₂ + C₃)) is inversely proportional to gas migration fluxes. The CH₄ “emission factor” (total measured output divided by investigated seepage area) was similar to that derived in other mud volcanoes of the same size and activity. The updated global “emission-factor” data-set, now including 27 mud volcanoes from different countries, suggests that previous estimates of global CH₄ emission from mud volcanoes may be significantly underestimated.