Interaction of the methane cycle and processes in wetland ecosystems in a climate model of intermediate complexity

The climate model of the Institute of Atmospheric Physics of the Russian Academy of Sciences (IAP RAS CM) has been supplemented with a module of soil thermal physics and the methane cycle, which takes into account the response of methane emissions from wetland ecosystems to climate changes. Methane emissions are allowed only from unfrozen top layers of the soil, with an additional constraint in the depth of the simulated layer. All wetland ecosystems are assumed to be water-saturated. The molar amount of the methane oxidized in the atmosphere is added to the simulated atmospheric concentration of CO₂. A control preindustrial experiment and a series of numerical experiments for the 17th–21st centuries were conducted with the model forced by greenhouse gases and tropospheric sulfate aerosols. It is shown that the IAP RAS CM generally reproduces preindustrial and current characteristics of both seasonal thawing/freezing of the soil and the methane cycle. During global warming in the 21st century, the permafrost area is reduced by four million square kilometers. By the end of the 21st century, methane emissions from wetland ecosystems amount to 130–140 Mt CH₄/year for the preindustrial and current period increase to 170–200 MtCH₄/year. In the aggressive anthropogenic forcing scenario A2, the atmospheric methane concentration grows steadily to ≈3900 ppb. In more moderate scenarios A1B and B1, the methane concentration increases until the mid-21st century, reaching ≈2100–2400 ppb, and then decreases. Methane oxidation in air results in a slight additional growth of the atmospheric concentration of carbon dioxide. Allowance for the interaction between processes in wetland ecosystems and the methane cycle in the IAP RAS CM leads to an additional atmospheric methane increase of 10–20% depending on the anthropogenic forcing scenario and the time. The causes of this additional increase are the temperature dependence of integral methane production and the longer duration of a warm period in the soil. However, the resulting enhancement of the instantaneous greenhouse radiative forcing of atmospheric methane and an increase in the mean surface air temperature are small (globally < 0.1 W/m² and 0.05 K, respectively).     

夏季长江口及其邻近海域挥发性卤代烃的分布和海-气通量研究

运用吹扫-捕集气相色谱法测定了2017年夏季长江口及其邻近海域海水中4种常见的挥发性卤代烃（VHCs,包括一氟三氯甲烷（CFC-11）、碘甲烷（CH₃I）、三氯甲烷（CH₃CCl₃）和四氯乙烯（C₂Cl₄））以及大气中CFC-11、CH₃I和C₂Cl₄的浓度。结果表明,表层海水中4种VHCs浓度的水平分布受长江径流输入影响强烈,整体上呈现近岸高、远海低的趋势。垂直方向上4种VHCs浓度最高值出现在10 m水层,长江口内断面的浓度整体高于口外断面的浓度。海水中VHCs的浓度分布受水文环境、生物释放和人为因素等的共同影响。相关性分析表明CH₃I与Chl a浓度不存在明显的相关性,而CFC-11与CH₃I、C₂Cl₄浓度存在显著相关性（P<0.01）,表明调查海域人为源对CH₃I和C₂Cl₄的影响大于天然源。大气中CFC-11、CH₃I和C₂Cl₄的浓度分布整体上呈现近岸高、远海低的趋势。CFC-11的浓度低于全球平均值,表明我国CFC-11的排放得到了有效控制。后向轨迹分析表明来自近岸的陆源污染物的扩散和输送是调查海域大气中3种VHCs的重要来源。CFC-11、CH₃I和C₂Cl₄的海-气通量平均值分别为24.99 nmol/（m2·d）、7.80 nmol/（m2·d）、1.55 nmol/（m2·d）,表明夏季长江口及其邻近海域是大气中这3种VHCs的源。     

Methane, carbon monoxide, and carbon dioxide concentrations measured in the atmospheric surface layer over continental Russia in the TROICA experiments

The principal statistical regularities typical of the behaviors of the CH₄, CO, and CO₂ concentrations in the atmospheric surface layer over the continental Russian territory are revealed from the measurements performed in 1997–2004 along the Trans-Siberian Railroad from Moscow to Khabarovsk with a mobile laboratory. The data obtained under the conditions of the atmosphere free of anthropogenic pollutants are analyzed. For near-background conditions, the typical continental methane, carbon monoxide, and carbon dioxide concentrations and characteristic features of their large-scale spatial distributions and daily variations, including those caused by surface inversions, are determined. Variations in the concentrations of these trace gases over industrial regions are analyzed. Our results are compared to the data obtained at background stations of the world network of atmospheric monitoring and to the data of a numerical simulation.     

Temporal variations in carbon dioxide and methane concentrations under urban conditions

Temporal variations in the surface concentrations of two greenhouse gases (carbon dioxide and methane) in the atmosphere over a large city are studied on the basis of the data obtained during the 2003–2005 observations at a Moscow station for environmental monitoring. This station is based on the TROICA mobile observatory and located at the meteorological station of the Faculty of Geography, Moscow State University, on Vorob’evy gory. The methods of isolating the background concentrations of greenhouse gases under urban conditions are proposed, and the excess concentrations of CO₂ and CH₄ over their background values are estimated for different seasons and times of day. The CO₂ and CH₄ concentrations are shown to have more pronounced diurnal cycles in summer than in winter. The main causes of temporal variations in the surface concentrations of CO₂ and CH₄ under urban conditions and the differences between the mean concentrations of these greenhouse gases in Moscow and other areas of Russia are analyzed. It is shown that variations in the surface concentrations of carbon dioxide and methane on different time scales are caused by different atmospheric processes (global circulation, mesoscale gravity waves, surface temperature inversions, etc.)     

西太平洋雅浦海沟区海水中CH4和DMSP的垂直变化特征

本研究首次探究了西太平洋雅浦海沟北段从表层到超深渊海水中甲烷（CH₄）及二甲基硫（DMS）的前体物质二甲基巯基丙酸内盐（DMSP）的浓度变化情况。结果表明:雅浦海沟海水甲烷浓度变化范围为1.49~3.87 nmol/L。其上层海水甲烷平均浓度最高,有明显的次表层极大现象。雅浦海沟氧最小层海水的甲烷平均浓度最低;在500~1 000 m中层水中甲烷浓度有一定程度的增大,1 000 m以下至底层甲烷浓度继续升高。研究海区溶解态DMSP（DMSPd）和总DMSP（DMSPt）平均浓度的垂直变化随深度呈先增大后减小趋势,颗粒态DMSP（DMSPp）的平均浓度随深度呈波动式变化,在中层达到最大。雅浦海沟CH₄和DMSP浓度垂直变化受浮游生物、微生物、光照、温度、压力、大洋环流等的复杂影响。在真光层海水中,CH₄浓度与DMSPd、DMSPp和DMSPt浓度表现为负相关关系,在200 m至底层海水中,CH₄浓度与DMSPd、DMSPp和DMSPt浓度表现为正相关关系,显示光照条件是造成雅浦海沟不同深度海水CH₄和DMSP浓度相关性差异的关键因素。     

Atmospheric remote sensing constraints on direct sea-air methane flux from the 22/4b North Sea massive blowout bubble plume

A new airborne remote sensing approach to estimate an upper limit of the direct sea-air methane emission flux was applied over the 22/4b blowout site located at N57.92°, E1.63° in the North Sea. Passive remote sensing data using sunglint/sunglitter geometry were collected during instrumental tests with the Methane Airborne MAPper – MAMAP – instrument installed aboard the Alfred Wegener Institute (AWI) Polar-5 aircraft on 3. June 2011. MAMAP is a passive short wave infrared (SWIR) remote sensing spectrometer for airborne measurements and retrieval of the atmospheric column-averaged dry air mole fractions of methane (XCH₄) and carbon dioxide (XCO₂). In addition to MAMAP a fast CH₄ in-situ analyzer (Los-Gatos Research Inc. RMT-200), two 5-hole turbulence probes and the Polar-5 basic sensor suite comprising different temperature, pressure, humidity and camera sensors were installed aboard the aircraft. The collected MAMAP remote sensing data acquired in the vicinity of the 22/4b blowout site showed no detectable increase in the derived XCH₄ (with respect to the atmospheric background). Based on the absence of a detectable XCH₄ column increase, an approximate top-down upper-limit for the direct atmospheric 22/4b blowout CH₄ emissions from the main bubble plume of less than 10 ktCH₄/yr has been derived. The constraint has been determined by comparing XCH₄ information derived by the remote sensing measurements with results obtained from a Gaussian plume forward model simulation taking into account the actual flight track, the instrument sensitivity and measurement geometry, as well as the prevailing atmospheric conditions.     

Time variability of the total methane content in the atmosphere over the vicinity of St. Petersburg

The results of measuring the methane content in the entire atmospheric thickness over the St. Petersburg region are given for 1991–2007. It is shown that, within this period, the mean annual cycle of the total methane content is characterized by its maximum values in December–January and its minimum values in June–August when the annual-cycle amplitude amounts to ∼3.6%. In this case, the annual variations in the total methane content may differ significantly from the mean annual cycle obtained in some years. A statistically significant linear trend of the total CH₄ content has not been revealed for 1991–2007. The obtained values of the linear-trend index have opposite signs in the winter and summer months (positive for January 0.6 ± 0.2%/year and February 0.4 ± 0.2%/year and negative for July 0.3 ± 0.2%/year and August 0.2 ± 0.1%/year). This fact suggests the tendency for an increase in the amplitude of the annual cycle of the total CH₄ content. The results of a spectral analysis of a series of data on the total CH₄ content show that, for 1991–2007, the following harmonics are pronounced with a confidence of 95%: 12 months (annual harmonic), 32 months (quasi-biennial oscillations), and 55 months (4.5 years), which are also pronounced in the series of meteorological parameters and total ozone content.     

Variations in the total column amounts of carbon monoxide and methane in the Antarctic atmosphere

The results of measuring the total contents of carbon monoxide and methane via the method of solar-absorption spectroscopy are presented. The measurements were performed at the Molodezhnaya Station in 1977–1978, at the Mirny Observatory from 1982 to 1992, and at the Novolazarevskaya Station from 2003 to 2006. The character of seasonal variations in the contents of these gases in the Antarctic atmosphere is described and compared to the intra-annual variation of their surface concentrations measured at the Syowa Station (Japan). Synchronous intra-annual variations in the contents of carbon monoxide in the atmospheric column and in its surface concentrations are observed, while the spring maximum content of methane is observed three months after the maximum of its surface concentration. Synchronous seasonal variations in the total content of methane and ozone are observed, which makes it possible to suggest that the Antarctic circumpolar vortex has a significant influence on the characteristics of the vertical distribution of methane during Antarctic spring. Quantitative estimates of the parameters of multiyear variations in the contents of CO and CH₄ are given. The content of methane was increasing (although with different rates) during the entire observation period 1977–2006. The content of CO was observed to increase until 1992 and to decrease during 2003–2006.     

Diverse methane concentrations in anoxic brines and underlying sediments,eastern Mediterranean Sea

Elevated methane (CH₄) concentrations (128–2692×10³ nM) occur in the hypersaline anoxic brine pools of Bannock and Urania Basins, eastern Mediterranean Sea, compared to low concentrations (17–80×10³ nM) in the sediments below the anoxic brines. The CH₄ enrichment in the brines might be due to the long residence time of the brine in the Basin. An attempt is made to determine the sources for the enriched dissolved CH₄ by considering the influence of hydrothermal activity, the occurrence of sapropel layers (biogenic) and dissolution of gas hydrates. Furthermore, it is suggested that the enriched CH₄ in Bannock and Urania Basins is diffused and mixed with the overlying waters by local upward transport mechanisms that selectively move CH₄ upward in these Basins.     

Atmospheric trace gas measurements during SEEDS-II over the northwestern pacific

Atmospheric trace gas measurements were conducted during SEEDS-II. Atmospheric dimethylsulfide (DMS) was continuously measured by GC-MS during the R/V Hakuho cruise. Further, ambient air was sampled into canisters (42 samples) and analyzed by GC-MS and GC-FID for various biogenic and anthropogenic volatile organic compounds (VOCs) after the cruise. CO, O₃, SO₂, and NOx were monitored continuously aboard the ship.A fertilization experiment was conducted in a high-nitrate, low-chlorophyll (HNLC) region (48°N, 165°E). The atmospheric concentrations inside a patch (fertilized area) were compared with those outside it (natural area); however, clear differences were not observed for biogenic trace gasses (DMS, CH₃Cl, CH₃I, isoprene, and alkenes) in the atmosphere. However, a high DMS concentration was observed over the northwestern Pacific Ocean. The fertilized area was also observed by R/V Kilo Moana, and DMS was measured by GC-FPD. A good agreement was observed between the results of the measurements made aboard the two independent ships by different measurement methods.The atmospheric SO₂ concentration was compared with the atmospheric DMS concentration. The SO₂ concentration was found to vary with the atmospheric DMS concentration. A diurnal variation of the atmospheric DMS concentration was observed around the fertilized region. The DMS content tends to increase during the night and decrease during the day. A box model calculation was conducted to explain the diurnal variation of the atmospheric DMS. Since there was no diurnal variation of the wind speed, a constant DMS flux from the ocean surface was assumed. Further, the atmospheric OH radical concentration was assumed to be dependent on sunlight. The box model can roughly reproduce the atmospheric DMS diurnal variation mainly caused by its removal reaction with OH radicals.     

Methane in the southern North Sea: Sources, spatial distribution and budgets

Measurements of methane (CH₄) so far have always shown supersaturation in the entire North Sea relative to the atmospheric partial pressure and the distribution of surface CH₄ reveals a distinct increase towards the shore. Since North Sea sediments presumably are an insignificant source for CH₄ the coastal contribution via rivers and tidal flats gains in importance.In this work, CH₄ data from the River Weser, the back barrier tidal flats of Spiekeroog Island (NW Germany), and the German Bight are presented. Results from the River Weser are compared to other rivers draining into the German Bight. Measurements in the tidal flat area of Spiekeroog Island highlight this ecosystem as an additional contributor to the overall CH₄ budget of the southern North Sea. A tidally driven CH₄ pattern is observed for the water column with maximum values during low tide. Tidal flat sediments turn out to be the dominating source because pore waters discharged during low tide are highly enriched in CH₄. In contrast, the freshwater contribution to the tidal flats by small coastal tributaries has almost no impact on water column CH₄ concentrations. The CH₄ level seems to be disturbed irregularly by wind forcing due to elevated degassing and prevention of advective flow when tidal flats remain covered by water.Based on our data, two model calculations were used to estimate the impact of tidal flats on the CH₄ budget in the German Bight. Our results demonstrate that the back barrier tidal flats of the east Frisian Wadden Sea contribute CH₄ in an order of magnitude between the Wash estuary and River Elbe and thus have to be considered in budget calculations.     

Spatial variation in shallow sediment methane sources and cycling on the Alaskan Beaufort Sea Shelf/Slope

The MITAS (Methane in the Arctic Shelf/Slope) expedition was conducted during September, 2009 onboard the U.S. Coast Guard Cutter (USCGC) Polar Sea (WAGB-11), on the Alaskan Shelf/Slope of the Beaufort Sea. Expedition goals were to investigate spatial variations in methane source(s), vertical methane flux in shallow sediments (<10 mbsf), and methane contributions to shallow sediment carbon cycling. Three nearshore to offshore transects were conducted across the slope at locations approximately 200 km apart in water column depths from 20 to 2100 m. Shallow sediments were collected by piston cores and vibracores and samples were analyzed for sediment headspace methane (CH₄), porewater sulfate (SO₄²⁻), chloride (Cl⁻), and dissolved inorganic carbon (DIC) concentrations, and CH₄ and DIC stable carbon isotope ratios (δ¹³C). Downward SO₄²⁻ diffusion rates estimated from sediment porewater SO₄²⁻ profiles were between −15.4 and −154.8 mmol m⁻² a⁻¹ and imply a large spatial variation in vertical CH₄ flux between transects in the study region. Lowest inferred CH₄ fluxes were estimated along the easternmost transect. Higher inferred CH₄ flux rates were observed in the western transects. Sediment headspace ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ values ranged from −138 to −48‰, suggesting strong differences in shallow sediment CH₄ cycling within and among sample locations. Measured porewater DIC concentrations ranged from 2.53 mM to 79.39 mM with δ¹³C_DIC values ranging from −36.4‰ to 5.1‰. Higher down-core DIC concentrations were observed to occur with lower δ¹³C where an increase in ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ was measured, indicating locations with active anaerobic oxidation of methane. Shallow core CH₄ production was inferred at the two western most transects (i.e. Thetis Island and Halkett) through observations of low ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ coupled with elevated DIC concentrations. At the easternmost Hammerhead transect and offshore locations, ${\mathrm{\delta }}^{13}{\text{C}}_{{\text{CH}}_4}$ and DIC concentrations were not coupled suggesting less rapid methane cycling. Results from the MITAS expedition represent one of the most comprehensive studies of methane source(s) and vertical methane flux in shallow sediments of the U.S. Alaskan Beaufort Shelf to date and show geospatially variable sediment methane flux that is highly influenced by the local geophysical environment.     

Methane in the Sevastopol coastal area, Black Sea

Concentrations of dissolved methane in seawater and bottom sediments, as well as of methane emanating from gas seeps were measured at 18 stations including several small bays in the Sevastopol coastal area (Black Sea) during 2007–2008. Methane concentrations in surface waters ranged from 10 to 2,970 nmol l^?1, and correlated well with values recorded for sediments. Methane concentrations in the water column were influenced by water depth, as well as by air and water temperatures. In the spring and summer of 2008, in situ CH₄ saturation relative to air was in the range of 970–71,900%. Maximum saturation was in summer. CH₄ fluxes to the atmosphere from the Sevastopol coastal area were estimated to vary from 190 to 1,550 μmol m^?2 day^?1. Gas bubbles escaping from the seepages contained about 57 vol% methane. Radiocarbon dating of the methane revealed an age not exceeding 150 years, implying a biogenic origin.     

Microbial processes of the carbon and sulfur cycles in the Kara Sea

The results of microbiological, biogeochemical, and isotope geochemical studies in the Kara Sea are described. The samples for these studies were obtained during the 54th voyage of the research vessel Akademik Mstislav Keldysh in September 2007. The studied area covered the northern, central, and southwestern parts of the Kara Sea and the Gulf of Ob. The quantitative characteristics of the total bacterial population and the activity of the microbial processes in the water column and bottom sediments were obtained. The total population of the bacterioplankton (BP) varied from 250000 cells/ml in the northern water area to 3000000 cells/ml in the Gulf of Ob. The BP population depended on the content of the water suspension. The net BP production was minimal in the central water area, amounting to 0.15–0.2 μg C/(l day), and maximal (0.5–0.75 μg C/(l day)) in the Gulf of Ob. The organic material at the majority of the stations in the Ob transect predominantly contained light carbon isotopes (−28.0 to −30.18‰) of terrigenous origin. The methane content in the surface water layer varied from 0.18 to 2.0 μl CH₄/l, and the methane oxidation rate changed in the range of 0.1–100 nl CH₄/(l day). The methane concentration in the upper sediment layer varied from 30 to 300 μl CH₄/dm³; the rate of the methanogenesis was 44 to 500 nl CH₄/(dm³ day) and that of the methane oxidation, 30 to 2000 nl CH₄/(dm³ day). The rate of the sulfate reduction varied from 4 to 184 μg S/(dm³ day).     

Carbon cycling within the upper methanogenic zone of continental rise sediments; An example from the methane-rich sediments overlying the Blake Ridge gas hydrate deposits

Data from piston cores collected from Carolina Rise and Blake Ridge, and from many DSDP/ODP sites indicate that extreme ¹³C-depletion of methane and ΣCO₂ occurs within the uppermost methanogenic zone of continental rise sediments. We infer that ¹³C-depleted methane is generated near the top of the methanogenic zone when carbon of ¹³C-depleted ΣCO₂, produced by microbially-mediated anaerobic methane oxidation, is recycled back to methane through CO₂ reduction. Interstitial water and gas samples were collected in 27 piston cores, 16 of which penetrated through the sulfate reduction zone into methane-bearing sediments of the Carolina Rise and Blake Ridge. Isotopic measurements (δ¹³C_CH4, δ¹³C_CO2, δD_CH4, and δD_H2O) indicate that this methane is microbial in origin, produced by microbially-mediated CO₂ reduction. Methane samples form two distinct isotopic pools. (1) Methane from a seafloor seep site shows a mean δ¹³C_CH4 value of − 69 ± 2%., mirroring values found at ≥ 160 mbsf from a nearby DSDP site. (2) Twenty, areally-separated sites (sample depth, 10 to 25 mbsf) have δ¹³C_CH4 values ranging from −85 to −103%., and δ¹³C_CO2 as negative as −48%.. The very low δ¹³C values from the methane and CO₂ pools highlight the importance of carbon cycling within continental rise sediments at and near the sulfate-methane boundary.     

天然气水合物赋存区甲烷渗漏活动的地球化学响应特征

综述了天然气水合物赋存区甲烷渗漏活动的地球化学响应指标的研究进展,分析了应用单一指标识别甲烷渗漏活动各自所存在的问题,包括浅表层沉积物孔隙水中CH_4、SO_4~(2–)、Cl~–等离子浓度随深度的变化;浅层沉积物全岩W_(TOC)(W表示质量分数,TOC表示总有机碳)和W_(TS)(TS表示总硫)之间的相关性及比值;自生碳酸盐岩δ~(13)C和δ~(18)O;自生矿物重晶石、黄铁矿、自生石膏的δ~(34)S;有孔虫壳体和生物标志化合物的δ~(13)C等。结果表明孔隙水中的CH_4、SO4_~(2–)浓度及溶解无机碳的碳同位素组成可以用来识别目前正在发生的甲烷渗漏活动;而沉积物中的WTS、自生矿物的δ~(34)S、钡含量及其异常峰值和生物标志化合物的δ~(13)C等指标的联合使用可以更真实准确地反映地质历史时期天然气水合物赋存区的甲烷渗漏活动。因此,在实际研究过程中,可将孔隙水和沉积物两种介质的多种指标相结合。随着非传统稳定同位素(Fe、Ca、Mg等)和沉积物氧化还原敏感元素(Mo、V、U等)等研究的发展,甲烷渗漏活动地球化学响应指标的研究也将得到拓展,而多种地球化学指标的联合使用将为天然气水合物勘探及其形成分解过程识别研究提供重要的科学依据。     

In situ hydrocarbon concentrations from pressurized cores in surface sediments, Northern Gulf of Mexico

Two newly developed coring devices, the Multi-Autoclave-Corer and the Dynamic Autoclave Piston Corer were deployed in shallow gas hydrate-bearing sediments in the northern Gulf of Mexico during research cruise SO174 (Oct–Nov 2003). For the first time, they enable the retrieval of near-surface sediment cores under ambient pressure. This enables the determination of in situ methane concentrations and amounts of gas hydrate in sediment depths where bottom water temperature and pressure changes most strongly influence gas/hydrate relationships. At seep sites of GC185 (Bush Hill) and the newly discovered sites at GC415, we determined the volume of low-weight hydrocarbons (C₁ through C₅) from nine pressurized cores via controlled degassing. The resulting in situ methane concentrations vary by two orders of magnitudes between 0.031 and 0.985 mol kg^− 1 pore water below the zone of sulfate depletion. This includes dissolved, free, and hydrate-bound CH₄. Combined with results from conventional cores, this establishes a variability of methane concentrations in close proximity to seep sites of five orders of magnitude. In total four out of nine pressure cores had CH₄ concentrations above equilibrium with gas hydrates. Two of them contain gas hydrate volumes of 15% (GC185) and 18% (GC415) of pore space. The measurements prove that the highest methane concentrations are not necessarily related to the highest advection rates. Brine advection inhibits gas hydrate stability a few centimeters below the sediment surface at the depth of anaerobic oxidation of methane and thus inhibits the storage of enhanced methane volumes. Here, computerized tomography (CT) of the pressure cores detected small amounts of free gas. This finding has major implications for methane distribution, possible consumption, and escape into the bottom water in fluid flow systems related to halokinesis.     

Expulsion of Shallow Gas in the Skagerrak—Evidence from Sub-bottom Profiling, Seismic, Hydroacoustical and Geochemical Data

A combined high resolution seismic, sub-bottom profiling, and multi-beam echo-sounding survey in the Skagerrak (Danish sector of the North Sea) together with gas analyses at a station along the profile exhibit the expulsion of gas (mainly methane) and the presence of gas-charged sediments at shallow depth. The echo-soundings yield detailed insight into the distribution and shape of typical sea-floor features associated with gas seepage, such as pockmarks. The pockmarks reach dimensions of 800 m in length, 300 m in width, and 15 m in depth, with the long axis running parallel to the slope of the Norwegian Trench. Processing of the multi-channel high resolution seismic data and the digitally recorded sub-bottom profiler signals indicate an internal compressional velocity of about 1050 m s^-1 within the gas-charged sediments reaching from the sea-floor to a sub-bottom depth of about 23 m. Using the lateral distribution and thickness of the gas-charged sediments in conjunction with a mean concentration of gas of 3000 ppb, the present amount of trapped gas is estimated to be 6·45 × 10¹¹ g CH₄. The flux of methane through the sea-bed into the water column appears to be 7·2 × 10¹⁰ g CH₄ per year. To explain the small difference in size between the methane pool in near-surface sediments and the annual flux through the sea-bed, a constantly high supply of methane from leaking hydrocarbon reservoirs at greater depths has to be active.     

Methane in the western North Pacific

The concentration of methane in about 400 seawater samples collected in the western North Pacific, mostly from 40°N to 5°S along 165°E was determined. While the concentration of methane in the surface water was slightly greater in the high-latitudes, it did not widely vary with a standard deviation of 0.29 n mol/l for a mean value of 2.49 n mol/l. The 90% confidence limit of the mean was 0.08 n mol/l. The degree of oversaturation in 1991 (31±4%) was not different from that in circa 1970. If we assume that this degree of oversaturation occurs in the entire oceans, the annual flux of methane becomes 6×10¹²g CH₄. Both the concentrations of methane and chlorophylla were higher in the surface 100 m layer. However, the correlation between them was not well in the entire surface waters. This may indicate that the production of methane is not directly related to the photosynthetic process. The concentration of methane decreased gradually with increasing depth down to 1000 m. Its horizontally and vertically uniform concentration in the abyssal water suggests that the turnover time of methane in the oxic pelagic water is in the range between a few years and a few hundred years.     

Estimates of methane output from mud extrusions at the erosive convergent margin off Costa Rica

Four mud extrusions were investigated along the erosive subduction zone off Costa Rica. Active fluid seepage from these structures is indicated by chemosynthetic communities, authigenic carbonates and methane plumes in the water column. We estimate the methane output from the individual mud extrusions using two independent approaches. The first is based on the amount of CH₄ that becomes anaerobically oxidized in the sediment beneath areas covered by chemosynthetic communities, which ranges from 10⁴ to 10⁵ mol yr^− 1. The remaining portion of CH₄, which is released into the ocean, has been estimated to be 10²–10⁴ mol yr^− 1 per mud extrusion. The second approach estimates the amount of CH₄ discharging into the water column based on measurements of the near-bottom methane distribution and current velocities. This approach yields estimates between 10⁴–10⁵ mol yr⁻¹. The discrepancy of the amount of CH₄ emitted into the bottom water derived from the two approaches hints to methane seepage that cannot be accounted for by faunal growth, e.g. focused fluid emission through channels in sediments and fractures in carbonates. Extrapolated over the 48 mud extrusions discovered off Costa Rica, we estimate a CH₄ output of 20·10⁶ mol yr^− 1 from mud extrusions along this 350 km long section of the continental margin. These estimates of methane emissions at an erosional continental margin are considerably lower than those reported from mud extrusion at accretionary and passive margins. Almost half of the continental margins are described as non-accretionary. Assuming that the moderate emission of methane at the mud extrusions off Costa Rica are typical for this kind of setting, then global estimates of methane emissions from submarine mud extrusions, which are based on data of mud extrusions located at accretionary and passive continental margins, appear to be significantly too high.