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.     

In situ evaluation of nearshore marine and fresh pore water transport into Flamengo Bay,Brazil

Transport between pore waters and overlying surface waters of Flamengo Bay near Ubatuba, Brazil, was quantified using natural and artificial geochemical tracers, ²²²Rn, Cl⁻, and SF₆, collected from multi-level piezometers installed along a transect perpendicular to the shore. Eight sampling ports positioned along the length of the piezometers allowed sampling of pore waters at discrete depth intervals from 10 to 230 cmbsf (centimeters below seafloor). Small volume samples were collected from the piezometers using a peristaltic pump to obtain pore water depth profiles. Pore water ²²²Rn is deficient in shallow sediments, allowing application of a diffusion-corrected ²²²Rn exchange rate. This model estimates the magnitude of pore water exchange rates to be about 130–419 cm/day. An SF₆-saturated fluorescein dye tracer was gently pumped into deep pore waters and exchange rates estimated from this method range from 29 to 185 cm/day. While absolute rates are higher using ²²²Rn than SF₆, rates are of similar magnitudes and the trends with distance from shore are the same – flow is greatest 6 m from shore and decreases by more than 50% further offshore. A Cl⁻ mass balance indicates the greatest fraction of fresh SGD occurs along an apparent preferential flow path in sediments within 5–7 m of the shoreline (87%). Recirculating bay waters through sediments dominate pore water advection at 10 m offshore where only 4% of the flow can be attributed to a freshwater source. Both fresh and marine sources combine to make up submarine groundwater discharge to coastal water bodies. The magnitude of fresh aquifer discharge is often a spatially variable and minor component of the total discharge.     

Effects of upwelling,tides and biological processes on the inorganic carbon system of a coastal lagoon in Baja California

The role of coastal lagoons and estuaries as sources or sinks of inorganic carbon in upwelling areas has not been fully understood. During the months of May–July, 2005, we studied the dissolved inorganic carbon system in a coastal lagoon of northwestern Mexico during the strongest period of upwelling events. Along the bay, different scenarios were observed for the distributions of pH, dissolved inorganic carbon (DIC) and apparent oxygen utilization (AOU) as a result of different combinations of upwelling intensity and tidal amplitude. DIC concentrations in the outer part of the bay were controlled by mixing processes. At the inner part of the bay DIC was as low as 1800 μmol kg⁻¹, most likely due to high water residence times and seagrass CO₂ uptake. It is estimated that 85% of San Quintín Bay, at the oceanic end, acted as a source of CO₂ to the atmosphere due to the inflow of CO₂-rich upwelled waters from the neighboring ocean with high positive fluxes higher than 30 mmol C m⁻² d⁻¹. In contrast, there was a net uptake of CO₂ and HCO₃⁻ by the seagrass bed Zostera marina in the inner part of the bay, so the pCO₂ in this zone was below the equilibrium value and slightly negative CO₂ fluxes of −6 mmol C m⁻² d⁻¹. Our positive NEP and ΔDIC values indicate that Bahía San Quintín was a net autotrophic system during the upwelling season during 2005.     

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 Izena Cauldron,Okinawa Trough

Methane in the deep water of Izena Cauldron (maximum depth: ca. 1650 m) at the east side of mid-Okinawa Trough was studied by casting a CTD system with 12 Niskin bottles for water sampling at 11 stations inside and outside the cauldron. The water contained much methane up to 706 nmoles/l. The depths of maximum concentration varied widely from station to station, indicating the existence of a considerable number of vents emitting methane and heat. The waters containing less methane formed a straight line in theT-S diagram, while those containing more methane were more largely deviated from the line. The temperature anomaly was virtually proportional to the methane concentration, suggesting that the oxidation rate of methane inside the cauldron is negligibly small and methane can be used as a tracer of the cauldron water. The relation and the estimated vertical diffusivity gave the following fluxes. The emissions of methane and heat out of the bottom below 1450 m turn out to be 1400 moles/day and 7×10¹⁰ cal/day, respectively. The total emission rates inside the cauldron are presumed to be about twice the above values. The turnover time of methane has been estimated to be 240 days, which is also that of heat generated from the bottom and probably that of the bottom water.     

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.     

Radium tracing of submarine groundwater discharge (SGD) and associated nutrient fluxes in a highly-permeable bed coastal zone, Korea

In order to estimate submarine groundwater discharge (SGD) and SGD-driven nutrient fluxes, we measured the concentrations of nutrients, ²²⁴Ra, and ²²⁶Ra in seawater, river water, and coastal groundwater of Yeongil Bay (in the southeastern coast of Korea) in August 2004 and February 2005. The bottom sediments over the shallow areas of this bay are composed mainly of coarse sands. Large excess concentrations of ²²⁴Ra, ²²⁶Ra, and Si supplied from SGD were observed in August 2004, while these excess concentrations were not apparent in February 2005. Based on the mass balance for ²²⁴Ra, ²²⁶Ra, and Si, which showed conservative mixing behavior in seawater, SGD was estimated to be approximately 6 × 10⁶ m³ day^− 1 (seepage rate = 0.2 m day^− 1) in shallow areas (< 9 m water depth) in August 2004, which is much higher than the SGD level typically found in other coastal regions worldwide. During the summer period, SGD-driven nutrients in this bay contributed approximately 98%, 12%, and 76% of the total inputs for dissolved inorganic nitrogen (DIN), phosphorus (DIP), and silicate (DSi), respectively. Our study implies that the ecosystem in this highly permeable bed coastal zone is influenced strongly by SGD during summer, while such influences are negligible in winter.     

Methane and methane carbon isotope ratios in the Northeast Atlantic including the Mid-Atlantic Ridge (50°N)

Previous work has shown that methane anomalies frequently occur within the rift valley of the Mid-Atlantic Ridge (MAR). The plumes appear confined within the high, steep walls of the valley, and it is not known whether methane may escape to the open ocean outside. In order to investigate this question, the concentration and ¹³C/¹²C ratio of methane together with CCl₃F concentration were measured in the northeastern Atlantic including the rift valley near 50°N. This segment contained methane plumes centered several 100 m above the valley floor with δ¹³C values mostly between –15‰ and –10‰. A limited number of helium isotope measurements showed that δ³He increased to 17% at the bottom of the valley, which suggests the helium and methane sources may be spatially separated. In the eastern Atlantic away from the ridge (48°N, 20°W), the methane concentration decreased monotonically from the surface to the bottom, but the methane δ¹³C exhibited a mid-water maximum of about –25‰. The bottom water methane contained a significantly lower δ¹³C of about –36‰. Thus, it appears that isotopically heavy methane escapes from the MAR into North Atlantic Deep Water (NADW) that contacts the ridge crest while circulating to the east. The formation of NADW supplies isotopically light methane that dilutes the input of heavy carbon from the ridge. We employed a time-dependent box model to calculate the extent of isotope dilution and thereby the flux of MAR methane into the NADW circulation. The degree of methane oxidation, which affects the ¹³C/¹²C of methane through kinetic isotope fractionation, was estimated by comparing methane and CFC-11 model results with observations. The model calculations indicate a MAR methane source of about 0.06×10⁻⁹ mol L⁻¹ yr⁻¹ to waters at the depth of the ridge crest. Assuming this extends to a 500 m thick layer over half of the entire Atlantic, the amount of methane escaping from the MAR to the open ocean is estimated to be about 1×10⁹ mol yr⁻¹. The total production of methane within the rift valley is likely much greater than the flux from the valley to the outside because of local oxidation. This implies that serpentinization of ultramafic rocks supports much of methane production in the rift valley because the amount expected from basalt degassing in association with mantle helium (<0.6×10⁹ mol CH₄ yr⁻¹) is less than even the net amount escaping from the valley. The model results also indicate the methane specific oxidation rate is about 0.05 yr⁻¹ in open waters of the northern Atlantic.     

海底地下水排放对典型红树林蓝碳收支的影响

海底地下水排放(Submarine Groundwater Discharge，SGD)是陆海相互作用的重要表现形式之一，其携带的物质对近岸海域生源要素的收支有重要影响。本文利用222Rn示踪技术估算了我国典型红树林海湾—广西珍珠湾在2019年枯季(1月)SGD携带的碳通量。调查发现，地下水中222Rn活度、溶解无机碳(DIC)和溶解有机碳(DOC)的平均浓度均高于河水和湾内表层海水。利用222Rn质量平衡模型估算得到珍珠湾SGD速率为(0.36±0.36) m/d，SGD输入到珍珠湾的DIC和DOC通量分别为(2.41±2.63)×107 mol/d和(1.96±2.20)×106 mol/d。珍珠湾溶解碳的源汇收支表明，SGD携带的DIC和DOC分别占珍珠湾总DIC和总DOC来源的91%和89%。因此，SGD携带的DIC和DOC是珍珠湾DIC和DOC的主要来源，是海岸带蓝碳收支和生物地球化学循环过程中的重要组成。     

~(35)SO_4~(2-)示踪法测定九龙江河口沉积中硫酸盐还原速率

在2011年7月利用35SO2-4培养示踪法测定九龙江河口两个站位(A站位位于咸淡混合区,盐度3~5;B站位位于海相区,盐度20~25)沉积柱中硫酸盐还原速率的垂直分布。结果显示A站位沉积柱中硫酸盐还原速率变化范围为54~2 345nmol/(cm3·d),从表层到底部先增大后减小,最大值出现在20cm深度附近;B站位硫酸盐还原速率在24~987nmol/(cm3·d)之间,分别在10cm和78cm深度附近出现两个峰值,分别为876nmol/(cm3·d)和987nmol/(cm3·d)。综合分析两个站位孔隙水中SO2-4、甲烷浓度和沉积物中总有机碳、温度和氧化还原电位的垂直变化趋势与其硫酸盐还原速率的分布规律,表明A站位沉积物中硫酸盐还原以有机矿化为主;B站位受到有机质矿化和甲烷厌氧氧化的共同作用;两个站位硫酸盐还原速率及垂直分布趋势受孔隙水中SO2-4浓度、有机质活性和温度的共同影响;根据各个层位硫酸盐还原速率估算两个站位硫酸盐还原通量(以硫计)分别为527.9mmol/(m2·d)和357.1mmol/(m2·d),表明硫酸盐还原是九龙江河口有机质厌氧矿化的重要路径。     

Vodyanitskii mud volcano,Sorokin trough,Black Sea: Geological characterization and quantification of gas bubble streams

Vodyanitskii mud volcano is located at a depth of about 2070 m in the Sorokin Trough, Black sea. It is a 500-m wide and 20-m high cone surrounded by a depression, which is typical of many mud volcanoes in the Black Sea. 75 kHz sidescan sonar show different generations of mud flows that include mud breccia, authigenic carbonates, and gas hydrates that were sampled by gravity coring. The fluids that flow through or erupt with the mud are enriched in chloride (up to ∼650 mmol L⁻¹ at ∼150-cm sediment depth) suggesting a deep source, which is similar to the fluids of the close-by Dvurechenskii mud volcano. Direct observation with the remotely operated vehicle Quest revealed gas bubbles emanating at two distinct sites at the crest of the mud volcano, which confirms earlier observations of bubble-induced hydroacoustic anomalies in echosounder records. The sediments at the main bubble emission site show a thermal anomaly with temperatures at ∼60 cm sediment depth that were 0.9 °C warmer than the bottom water. Chemical and isotopic analyses of the emanated gas revealed that it consisted primarily of methane (99.8%) and was of microbial origin (δD-CH₄ = −170.8‰ (SMOW), δ¹³C-CH₄ = −61.0‰ (V-PDB), δ¹³C-C₂H₆ = −44.0‰ (V-PDB)). The gas flux was estimated using the video observations of the ROV. Assuming that the flux is constant with time, about 0.9 ± 0.5 × 10⁶ mol of methane is released every year. This value is of the same order-of-magnitude as reported fluxes of dissolved methane released with pore water at other mud volcanoes. This suggests that bubble emanation is a significant pathway transporting methane from the sediments into the water column.     

Effects of Benthic Flux on Short Term Variations of Nutrients in Aburatsubo Bay

In order to investigate effects of benthic flux on the short-term variations in the distribution of nutrients in coastal waters, the concentrations of nutrients (PO₄ ^3-, NH₄ ⁺ NO₃ ^-, NO₂ ^- and H₄SiO₄) and other oceanographic parameters were measured every three hours over a 24-hour period at four fixed stations in the water column of Aburatsubo Bay, a shallow semi-enclosed inlet. Sediment cores were also taken from a fixed station once in each season over one year to quantitatively determine their benthic flux. Consistent linear negative correlations were found between their concentrations and salinity in the surface layers. This result suggests that fresh water was the main source of these nutrients and a physical mixing was the major process controlling their distribution. Monthly variations of PO₄ ^3- and NH₄ ⁺ monitored for 18 months in the bay also indicate that the high surf concentration of these nutrients was associated with the appearance of low salinity waters. On the other hand, in the bottom layers, a linear correlation between the concentration of the nutrients and salinity became weak, especially for NH₄ ⁺ and PO₄ ^3-. Their concentrations were higher than the predicted value from the conservative mixing between the fresh water and seawater, indicating the possibility of another source in the bottom layers. Benthic flux is suggested as a possible source. Pore water profiles of NH₄ ⁺ and PO₄ ^3- indicate their flux towards the overlying seawater, which is quantitatively consistent with their water column distributions.     

Radium mass-balance in Jamaica Bay, NY: Evidence for a substantial flux of submarine groundwater

A mass balance for the naturally-occurring radium isotopes (²²⁴Ra, ²²³Ra, ²²⁸Ra, and ²²⁶Ra) in Jamaica Bay, NY, was conducted by directly estimating the individual Ra contributions of wastewater discharge, diffusion from fine-grained subtidal sediments, water percolation through marshes, desorption from resuspended particles, and water exchange at the inlet. The mass balance revealed a major unknown source term accounting for 19–71% of the total Ra input, which could only be resolved by invoking a source from submarine groundwater. Shallow (< 2 m depth) groundwater from permeable sediments in Jamaica Bay was brackish and enriched in Ra relative to surface bay waters by over two orders of magnitude. To balance Ra fluxes, a submarine groundwater input of 0.8 × 10⁹–9.0 × 10⁹ L d^− 1 was required. This flux was similar for all four isotopes, with individual estimates varying by less than a factor of 2. Our calculated groundwater flux was 6- to 70-fold higher than the fresh groundwater discharge to the bay estimated by hydrological methods, but closely matched direct flow rates measured with seepage meters. This suggests that a substantial portion of the discharge consisted of recirculated seawater. The magnitude of submarine groundwater discharge varied seasonally, in the order: summer > autumn > spring. Chemical analyses suggest that the recirculated seawater component of submarine groundwater delivers as much dissolved nitrogen to the bay as the fresh groundwater flux.     

High-resolution mapping of shallow gas accumulations and gas seeps in San Simón Bay (Ría de Vigo, NW Spain). Some quantitative data

San Simón Bay in the innermost part of the Ría de Vigo is characterized by an abundance of very shallow gas accumulations and methane seeps. During the expeditions of April–June–September 2004 within the Spanish-funded Gs2G project, detailed very high-resolution seismic and field investigations were carried out to study the shallow gas and the seeps. Direct gas fluxes also were measured from bubble streams. For the first time, the surface area and gas front depth of a shallow gas field has been mapped and quantified in the inner bay of Ría de Vigo. This field overlaps spatially with the distribution of Holocene mud within the bay. Seismic data show 3.6 km² affected by acoustic turbidity but this surface can be extended up to 9.5 km² of San Simón’s muddy subtidal area. Mounded turbidity superimposed on the main gas field has been mapped and characterized as anthropogenically (mussel rafts) mediated gas accumulations. Different acoustic anomalies have been identified and interpreted as being due to gas escapes from the present seabed sediment. The very high resolution of the seismic data makes it possible to identify a new type of seep, here named ‘acoustic smoke.’ A direct relationship can be observed between the gas front of accumulations and escape features, both acoustic seeps and pockmarks. The methane flux has been estimated from the subtidal environment in San Simón based on detected acoustic targets and direct measurements of current bubble flow. The total estimated methane flux from the seabed into the water column ranges from 10.1 to 48.8 t/year, and into the atmosphere from 7.0 to 34.2 t/year. The intertidal San Simón environment is also actively venting methane, as indicated by the presence of bubbling during high tide and white patches of Beggiatoa sp.     

Distributions, sources and atmospheric fluxes of nitrous oxide in Jiaozhou Bay

The distributions, sources and atmospheric fluxes of nitrous oxide (N₂O) in the seawater of Jiaozhou Bay were investigated during four surveys in 2003 to evaluate this area as a source of N₂O to the atmosphere. N₂O concentrations in both the surface and bottom waters of Jiaozhou Bay showed obvious variability with both seasons and tidal cycles. Atmospheric fluxes of N₂O in Jiaozhou Bay showed seasonal and spatial variations, with the highest values occurring in summer and the lowest in winter. The annual emission of N₂O from the bay was estimated to be 1.09 × 10⁶–2.23 × 10⁶ mol yr⁻¹. N₂O in the water column of Jiaozhou Bay was found to come from several external sources including riverine water, sewage water and groundwater input, among which the riverine input was dominant while the groundwater input was rather limited. The spatial variation in distribution and atmospheric fluxes of N₂O in Jiaozhou Bay was influenced by the input of polluted river waters and sewage effluent along the eastern coast, which highlights the effects of human impacts on N₂O emission rates.     

Sequentially sampled gas hydrate water,coupled with pore water and bottom water isotopic and ionic signatures at the Kukuy mud volcano,Lake Baikal: ambiguous deep-rooted source of hydrate-forming water

The isotopic and ionic composition of pure gas hydrate (GH) water was examined for GHs recovered in three gravity cores (165–193 cm length) from the Kukuy K-9 mud volcano (MV) in Lake Baikal. A massive GH sample from core St6GC4 (143–165 cm core depth interval) was dissociated progressively over 6 h in a closed glass chamber, and 11 sequentially collected fractions of dissociated GH water analyzed. Their hydrogen and oxygen isotopic compositions, and the concentrations of Cl^– and HCO₃ ^– remained essentially constant over time, except that the fraction collected during the first 50 minutes deviated partly from this pattern. Fraction #1 had a substantially higher Cl^– concentration, similar to that of pore water sampled immediately above (135–142 cm core depth) the main GH-bearing interval in that core. Like the subsequent fractions, however, the HCO₃ ^– concentration was markedly lower than that of pore water. For the GH water fractions #2 to #11, an essentially constant HCO₃ ^–/Cl^– ratio of 305 differed markedly from downcore pore water HCO₃ ^–/Cl^– ratios of 63–99. Evidently, contamination of the extracted GH water by ambient pore water probably adhered to the massive GH sample was satisfactorily restricted to the initial phase of GH dissociation. The hydrogen and oxygen isotopic composition of hydrate-forming water was estimated using the measured isotopic composition of extracted GH water combined with known isotopic fractionation factors between GH and GH-forming water. Estimated δD of ?126 to ?133‰ and δ¹⁸O of ?15.7 to ?16.7‰ differed partly from the corresponding signatures of ambient pore water (δD of ?123‰, δ¹⁸O of ?15.6‰) and of lake bottom water (δD of ?121‰, δ¹⁸O of ?15.8‰) at the St6GC4 coring site, suggesting that the GH was not formed from those waters. Observations of breccias in that core point to a possible deep-rooted water source, consistent with published thermal measurements for the neighboring Kukuy K-2 MV. By contrast, the pore waters of core St6GC4 and also of the neighboring cores GC2 and GC3 from the Kukuy K-9 MV show neither isotopic nor ionic evidence of such a source (e.g., elevated sulfate concentration). These findings constrain GH formation to earlier times, but a deep-rooted source of hydrate-forming water remains ambiguous. A possible long-term dampening of key deep-water source signatures deserves further attention, notably in terms of diffusion and/or advection, as well as anaerobic oxidation of methane.     

Remineralization and accumulation of organic carbon and nitrogen in marine sediments of eutrophic bays: the case of the Bay of Concepcion, Chile

The Bay of Concepcion (36°40′S; 73°02′W) is a semi-enclosed and shallow embayment in which biogeochemical processes are seasonally coupled to coastal upwelling during the austral spring and summer. The nutrient cycle in the bay is complex due to the combined effects of a pronounced O₂ minimum layer and high nutrient concentrations both originating from subsurface equatorial water during coastal upwelling and a rapid rate of sediment nutrient recycling. The sediments are characterized by a high content of organic matter mainly due to the extremely high rates of phytoplankton production and deposition. During the upwelling period, a black flocculent layer frequently covers the sediment–water interface in the inner part of the bay where an extensive mat of Beggiatoa spp. develops. Three approaches are used to analyse the extent to which the benthic system recycles or retains nutrients at two stations, located at the centre (station C, St. C) and mouth (station B, St. B) of the bay for a 1-year period (March 1996–1997): (1) estimation of C and N remineralization rates based on SO₄²⁻ reduction measurements, (2) calculation of C and N turnover rates using a diagenetic model applied to total organic carbon and total nitrogen vertical distributions and, (3) construction of C and N budgets from direct measurements of sedimentation (from a sediment trap) and estimates of the C and N burial rates. Depth-integrated SO₄²⁻ reduction rates varied between 3.4 (winter) and 25.5 (summer) mmol m⁻² d⁻¹. Estimated C and N oxidation rates ranged between 7.9 and 87.8 mol C m⁻² yr⁻¹ and between 0.9 and 6.9 mol N m⁻² yr⁻¹, respectively. Each approach yielded minor differences in the C and N remineralization rates (and also minor differences between both studied stations), except when the kinetic model was applied to C and N distribution without including the presence of the flocculent layer. The rates of carbon oxidation and sulphate reduction were considerably higher than in other coastal sediments with similar depositional regime. The C and N burial rates were 2.23 and 0.21 (St. C) and 1.30 and 0.09 (St. B) mol m⁻² yr⁻¹, respectively. The C/N ratio of the buried fraction was ca. 10.6 at St. C and 14.4 at St. B. Because the observed differences in burial rates could not be ascribed to distinctive depositional (both stations have similar sediment accumulation rates) and oceanographic (similar O₂ concentration and hydrography) conditions, differences may be due to in part spatial heterogeneity in the supply of organic matter. The degree of preservation of organic matter as plankton detritus and nitrogen accumulating bacterial biomass associated with Beggiatoa spp. at St. C may also be involved.     

The distribution of methane in the Tōkyō-wan

Eleven stations were occupied in the Tokyo-wan during a study on the distribution of methane in this autrophic coastal environment in August of 1993.The principal features of the observed methane included the following 6 points: (1) Excess methane in the surface layer from 1.5 times to greater than 25 times solubility equilibrium with the atmosphere.(2) The methane concentration in the upper water displayed a maximum wne around Station 5 and the second highest in bottom water at Stations 1 and 2,probably because there was the front resulting from the chemical processes.(3) Cotrelations between methane and other parameters exhibited correspondences and the methane distribution being mainly controlled by physical processes.(4) In some'stations,vertical profiles revealed associations between methane and Chl a and the relationships between methane with Chl a or nitrite have shown good linear cortelations.It is postulated that some methane is formed in situ.(5) The calculated flux of methane acrbss the air-sea interface was about 71 μmol/(m²·d).(6) Some methane might be produced along with the organic matter decomposition in bottom water.Others might be due to the methane fluxes into the bottom water from the anoxic sediment inside the bay,which are believed to be the main methane source.     

Authigenic Mg-calcite at a cold methane seep site in the Laptev Sea

Authigenic minerals were studied in Holocene shelf sediments of the Laptev Sea (cold methane seep site, water depth 71 m). The study presents the first finds of large hard carbonate concretions with Mg-calcite cement in recent sediments of the Arctic shelf seas. These concretions differ from previously reported glendonites and concretions from bottom sediments of the White Sea, Kara Sea, Sea of Okhotsk, etc. A study of the morphology, microstructure, and composition of these newly reported concretions revealed the multistage formation of carbonates (structural varieties of Mg-calcite and aragonite). It was shown that organic matter played an important role in the formation of authigenic carbonates, i.e., in the formation of sedimentary–diagenetic Mg-calcite. The role of methane as a possible source for authigenic carbonate formation was estimated. It was found that methane-derived Mg-calcite accounts for 17–35% of concretion materials. Mg-calcite had δ¹³С-С_carb values between–24 and–23‰ and δ¹³С-С_org values between–44.5 and–88.5‰.     

Stable Carbon and Nitrogen Isotopic Characterization of Organic Matter in a Mangrove Ecosystem on the Southwestern Coast of Thailand

Organic matter in a tropical mangrove ecosystem was characterized by stable carbon and nitrogen isotopic analyze, conducted on various organic samples, including land and mangrove plants, soils, particulate organic matter (POM), and sea and river sediments along the southwestern coast of Thailand. The δ¹³C values of land plants and POM in river water can be explained in terms of a greater influence of C₃ plants than C₄ plants in this area. The POM and sediments from the Trang River and Ko Talibong area showed systematically higher δ¹⁵N values than those from Ko Muk and other coastal areas. Organic matter in the Trang River might be influenced by nitrogen released from agricultural or human waste, which could affect the isotopic composition of POM and sediments in the Trang River estuary and along the coast near the river mouth. We used a stochastic method to estimate the contributions of four organic end-members, identifiable by their δ¹³C and δ¹⁵N values. The results implied that seagrasses were a major source of sedimentary organic matter, contributing 42 ± 5% in the Ko Muk area and 36 ± 5% in the Ko Talibong area. The contribution of coastal POM to sediments was estimated to be only 13% in Ko Muk and 19% in Ko Talibong. Mangrove plants contributed approximately 23% in both areas. It was concluded that seagrasses are an important source of sedimentary organic matter in this coastal region of southwestern Thailand. This revised version was published online in August 2006 with corrections to the Cover Date.