Molecular and isotopic characteristics of gas hydrate-bound hydrocarbons in southern and central Lake Baikal

We investigated the molecular composition (methane, ethane, and propane) and stable isotope composition (methane and ethane) of hydrate-bound gas in sediments of Lake Baikal. Hydrate-bearing sediment cores were retrieved from eight gas seep sites, located in the southern and central Baikal basins. Empirical classification of the methane stable isotopes (δ¹³C and δD) for all the seep sites indicated the dominant microbial origin of methane via methyl-type fermentation; however, a mixture of thermogenic and microbial gases resulted in relatively high methane δ¹³C signatures at two sites where ethane δ¹³C indicated a typical thermogenic origin. At one of the sites in the southern Baikal basin, we found gas hydrates of enclathrated microbial ethane in which ¹³C and deuterium were both highly depleted (mean δ¹³C and δD of –61.6‰ V-PDB and –285.4‰ V-SMOW, respectively). To the best of our knowledge, this is the first report of C₂ δ¹³C–δD classification for hydrate-bound gas in either freshwater or marine environments.     

Isotopic composition of dissolved inorganic carbon in subsurface sediments of gas hydrate-bearing mud volcanoes, Lake Baikal: implications for methane and carbonate origin

We report on the isotopic composition of dissolved inorganic carbon (DIC) in pore-water samples recovered by gravity coring from near-bottom sediments at gas hydrate-bearing mud volcanoes/gas flares (Malenky, Peschanka, Peschanka 2, Goloustnoe, and Irkutsk) in the Southern Basin of Lake Baikal. The δ¹³C values of DIC become heavier with increasing subbottom depth, and vary between ?9.5 and +21.4‰ PDB. Enrichment of DIC in ¹³C indicates active methane generation in anaerobic environments near the lake bottom. These data confirm our previous assumption that crystallization of carbonates (siderites) in subsurface sediments is a result of methane generation. Types of methanogenesis (microbial methyl-type fermentation versus CO₂-reduction) were revealed by determining the offset of δ¹³C between dissolved CH₄ and CO₂, and also by using δ¹³C and δD values of dissolved methane present in the pore waters. Results show that both mechanisms are most likely responsible for methane generation at the investigated locations.     

海水中溶解态铵盐氮同位素分析的预处理方法

以蒸馏法为基础, 研究了适合海水中铵盐稳定氮同位素分析的预处理方法。对蒸馏法预处理过程中的最佳蒸馏时间、沸石的选取、铵盐最适浓度范围等分别进行改进和优化, 获得稳定、高效的海水中铵盐氮稳定同位素分析预处理方法。结果表明: 最佳蒸馏时间为50 min, 铵盐的回收率为(97±5.8)%。测定了不同沸石对不同浓度氨氮的吸附率, 筛选出酸性条件下铵氮吸附效率较高且稳定的康华科技沸石; 确定铵盐的最佳适用浓度范围为2～10 μmol/L, 在该浓度范围内氮回收率94%～99%,氮分馏系数为0.1‰～0.8‰。将此方法应用于长江口海域水样分析, 结果表明, 这一方法可以应用于河口中铵盐的氮同位素分析, 能够为河口中溶解态氮的来源及循环机理等研究提供有效信息。     

Multi-frequency seismic study of gas hydrate-bearing sediments in Lake Baikal,Siberia

In this paper we present and discuss the frequency-dependent behaviour of the acoustic characteristics of methane hydrate-bearing sediments in Lake Baikal, Siberia. Five different types of seismic sources (airgun-array, two types of single airguns, watergun and sparker) are used, encompassing a frequency bandwidth from 10 up to 1000 Hz. On low-frequency airgun-array data, the base of the hydrate stability zone (HSZ) is observed as a high-amplitude bottom-simulating reflection (BSR) with reversed polarity. The amplitude and continuity of the BSR decrease or even disappear on medium- to high-frequency data, a feature explained in terms of vertical and horizontal resolution. The increasing reflection amplitude of the BSR with increasing offset, the calculated reflection coefficient of the BSR and the occurrence of enhanced reflections below the BSR suggest the presence of free gas below the HSZ. The observation of some enhanced reflections extending above the BSR may be interpreted as an indication for free gas co-existing with hydrates within the HSZ. Amplitude blanking above the BSR is highly variable while the BSR itself appears to act as a low-pass frequency filter for medium- to high-frequency data.New single-channel airgun profiles provide the first seismic information across the Baikal Drilling Project (BDP-97) deep drilling site, at which hydrate-bearing sediments were retrieved at about 200 m above the base of the local HSZ. At the drilling site there are no seismic characteristics indicative of the presence of hydrates. Combination of the drilling and seismic information has allowed us to make a rough estimation of the volume of hydrates and carbon stored in the sediments of Lake Baikal, which lead us to conclude that the Lake Baikal gas hydrate reservoirs do not form a prospective energy resource.     

Variations in the elemental composition of ferromanganese structures from Lake Baikal

The elemental composition of ferromanganese sedimentary structures from the bottom of Lake Baikal represented by nodules and crusts, as well as the enclosing sediments, have been studied by the atomic absorption, chemical, and ICP-MS methods. It is established that the contents of the rock-forming and accompanying elements in them are highly variable. In this connection, the examined samples are divided in two groups differing by their Mn/Fe values. In most of the samples, they range from 0.01 to 0.1, although some of the ferromanganese structures or their parts are substantially enriched in manganese. The contents of most of the rare and dispersed elements in the ferromanganese structures are usually at the background level, although the samples maximally enriched in iron or manganese are characterized by relatively high copper, nickel, cobalt, vanadium, zinc, and molybdenum concentrations.     

Stratigraphic and structural control on the distribution of gas hydrates and active gas seeps on the Posolsky Bank, Lake Baikal

The distribution and origin of shallow gas seeps in the vicinity of the Posolsky Bank in Lake Baikal were studied based on the integration of detailed seismic, multibeam, and hydro-acoustic water-column investigations. In all, 65 acoustic flares have been detected on the Posolsky Fault scarp near the crest of the bank and in a similar, nearby setting at water depths of ?43 to ?332?m. The seismic data reveal BSRs (bottom-simulating reflectors) occurring up to water depths of ?300?m. Calculations involving hydrate stability, heat flow, and topographic modulation based on BSR occurrence and multibeam bathymetry enabled prediction of a methane–ethane gas mixture and heat-flow values that would account for gas hydrate stability in the lake sediments under prevailing ambient conditions. These predictions are supported by ground truth data. The findings suggest that seeps concentrated along the crest of the Posolsky Bank are fed mainly by gas coming from below the base of the gas hydrate stability zone, which would migrate updip via permeable stratigraphic pathways beneath the bank. Gas would ultimately be released into the water column where these pathways are cut off by faults.

铵锌镉还原法测试硝酸盐氮、氧同位素方法研究

本研究利用铵锌镉还原法将海水、湖水和自来水水体中硝酸盐转化为N₂O气体测试氮、氧同位素, 结果表明当反应体系的pH值在6～8之间, NO₃^-还原为NO₂^-的转化率大于95%, NO₂^-还原为N₂O的转化率大于99%。配置5种丰度的硝酸盐氮、氧同位素标样, 将实验结果与理论值绘制校准曲线, 氮同位素校准曲线斜率为0.48, 相关性良好(R²=0.999 8), 5种丰度δ¹⁵N_N2O标准偏差在0.18‰～0.43‰之间(n=5);氧同位素校准曲线斜率为0.70, 相关性良好(R²=0.999 6), 5种丰度δ¹⁸O_N2O标准偏差在0.27‰～0.46‰之间(n=5)。铵锌镉还原法与镉柱还原法测定硝酸盐氮、氧同位素结果的精密度和准确度一致, 同时海水、湖水和自来水3种不同类型水样的硝酸盐氮、氧同位素测试数据满足实验要求, 而且在实验流程的简洁性和高效性方面更具优势。     

三价钛还原法分析硝酸根氮氧同位素的方法研究

本研究利用三价钛还原法将标准样品、海水、湖水和雨水中硝酸根转化为N₂O测试其氮氧同位素值,并优化实验条件（NO^-₃浓度、试剂量、反应时间和温度等）。结果表明：4 cm³硝酸根水样（浓度约为20 μmol/dm³）,加入100 mm³TiCl₃溶液（浓度为150 g/dm³）,25 ℃反应24 h,NO^-₃还原为N₂O的平均转化率为86.3%（n=5）。5种丰度硝酸根氮氧同位素标样校准曲线斜率分别为0.947和0.617,相关系数R²分别为0.999和0.994;方法检出限的NO^-3浓度为2.5 μmol/dm³,其δ¹⁵N的标准偏差小于0.7‰(n=5),δ¹⁸O_VSMOW值的标准偏差小于2.5‰(n=5);20 μmol/dm³硝酸根样品δ¹⁵N的标准偏差小于0.5‰（n=5),δ¹⁸O_VSMOW值的标准偏差小于1.0‰（n=5）。该方法测定3种不同类型水样δ¹⁵N的标准偏差分别为0.3‰、0.6‰和0.5‰;δ¹⁸O_VSMOW的标准偏差分别为2.1‰、2.0‰和1.6‰。三价钛还原法分析水体中硝酸根氮氧同位素操作步骤简单,测试效率高,但氧同位素结果需要系统校正。     

Thermal anomalies associated with shallow gas hydrates in the K-2 mud volcano, Lake Baikal

Thermal measurements and hydrate mapping in the vicinity of the K-2 mud volcano in Lake Baikal have revealed a particular type of association of thermal anomalies (29–121?mW?m^–2) near hydrate-forming layers. Detailed coring within K-2 showed that hydrates are restricted to two distinct zones at sub-bottom depths exceeding 70–300?cm. Temperature data from stations with hydrate recovery and degassing features all display low thermal gradients. Otherwise, the thermal gradients within the mud volcano are generally increased. These findings imply a more complicated thermal regime than often assumed for mud volcanoes, with important roles for both fluids and hydrates. The coexistence of neighbouring low and high thermal anomalies is interpreted to result from discharging and recharging fluid activity, rather than hydrate thermodynamics. It is suggested that hydrates play a key role in controlling the fluid circulation pattern at an early stage. At a later stage, the inflow of undersaturated lake water would favour the dissolution of structure I hydrates and the formation of structure II hydrates, the latter having been observed on top of structure I hydrates in the K-2 mud volcano.     

The nitrogen isotopic composition of dissolved nitrate in the Yangtze River (Changjiang) estuary,China

The nitrogen isotopic composition of dissolved nitrate (δ¹⁵N-NO₃⁻) in surface water of the Yangtze River estuary was determined in four seasons of 2006. δ¹⁵N-NO₃⁻ ranged from 0.4‰ to 6.5‰ and varied with seasons and geographic regions, reflecting the dynamics of nitrogen cycling in the estuarine ecosystem. δ¹⁵N-NO₃⁻ was markedly lower in February than in other seasons and exhibited conservative mixing, which was probably attributed to the NO₃⁻ being sourced from the atmospheric deposition and agricultural fertilizer. In the upper estuary, the influence of riverine inputs was important during all surveys. In the turbidity maximum zone, nitrification was found with nitrate depleted in ¹⁵N in May, whereas denitrification resulting in heavy δ¹⁵N-NO₃⁻ played an important role in August. More enriched δ¹⁵N-NO₃⁻ values coinciding with losses of nitrate concentrations based on the conservative mixing model were found in the adjacent marine area in May, and may reflect obvious phytoplankton assimilation of dissolved nitrate. In this manner, δ¹⁵N-NO₃⁻ may be a sensitive indicator of nitrogen sources and biogeochemical processing existing in this estuary in conjunction with the variations of dissolved nitrate and other environmental factors.     

A method to measure the isotopic (C) composition of dissolved organic carbon using a high temperature combustion instrument

The stable isotopes of dissolved organic carbon (DOC) are a powerful tool for distinguishing sources and inputs of organic matter in aquatic systems. While several methods exist to perform these analyses, no labs routinely utilize a high temperature combustion (HTC) instrument. Advantages of HTC instruments include rapid analysis, small sample volumes and minimal sample preparation, making them the favored devices for most routine oceanic DOC concentration measurements. We developed a stable carbon DOC method based around an HTC system. This method has the benefit of a simple setup, requiring neither vacuum nor high pressures. The main drawback of the method is a significant blank, requiring careful accounting of all blank sources for accurate isotopic and concentration values. We present here a series of experiments to determine the magnitude, source and isotopic composition of the HTC blank. Over time, the blank is very stable at  20 ng of carbon with a δ¹³C of − 18.1‰ vs. VPDB. The similarity of the isotopic composition of the blank and seawater samples makes corrections relatively minor. The precision of the method was determined by oxidizing organic standards with a wide isotopic and concentration range (− 9‰ to − 39‰; 18 μM to 124 μM). Analysis of seawater samples demonstrates the accuracy for low concentration, high salinity samples. The overall error on the measurement is approximately ± 0.8‰.     

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.     

Molecular and isotopic compositions of bitumens in Silurian tar sands from the Tarim Basin,NW China: Characterizing biodegradation and hydrocarbon charging in an old composite basin

Biodegradation and oil mixing in Silurian sandstone reservoirs of the Tarim Basin, one of the largest composite basins in China, were investigated by analyzing the molecular characteristics and stable carbon isotopic signatures of low-molecular-weight (LMW) saturated hydrocarbons and high-molecular-weight (HMW) asphaltenes. Detection of 25-norhopanes and 17-nortricyclic terpanes in most Silurian tar sands from the Tabei Uplift in the Tarim Basin suggests a much greater degree of biodegradation here than in the Tazhong Uplift. This explains the relatively more abundant tricyclic terpanes, gammacerane, pregnane and diasteranes in tar sands from the Tabei Uplift than in those from the Tazhong Uplift. Hence, care must be taken when assigning oil source correlations using biomarkers in tar sands because of the biodegradation and mixing of oils derived from multiple sources in such an old composite basin. Asphaltenes in the tar sands seem to be part of the oil charge before biodegradation, depending on the relative anti-biodegradation characteristics of asphaltenes, the similarity in carbon isotopic signatures for asphaltenes and their pyrolysates, and the consistent product distribution for flash pyrolysis and for regular steranes in asphaltene pyrolysates, regardless of whether the tar sands were charged with fresh oil. According to the relative distributions of regular steranes and the relatively abundant 1,2,3,4-tetramethylbenzene significantly enriched in ¹³C, the oil sources for asphaltenes in the tar sands might be related to lower Paleozoic marine source rocks formed in euxinic conditions. Nevertheless, the relatively low abundance of gammacerane and C₂₈ regular steranes observed in asphaltene pyrolysates and residual hydrocarbons, within limited samples investigated in this work, made a direct correlation of oils originally charged into Silurian tar sands with those Cambrian source rocks, reported so far, seem not to be possible. Comparison of carbon isotopic signatures of n-alkanes in asphaltene pyrolysates with those of LMW saturated hydrocarbons is helpful in determining if the abundant n-alkanes in tar sands are derived from fresh oil charges after biodegradation. The limited carbon isotopic data for n-alkanes in LMW saturated hydrocarbons from the tar sands can be used to classify oils charged after biodegradation in the composite basin into four distinct groups.     

An improved method for the hydrolysis and MBTH analysis of dissolved and particulate carbohydrates in seawater

An improved method for the bulk characterization of particulate and dissolved combined carbohydrates in seawater is presented. Seawater samples are dried under vacuum and the residue is hydrolyzed with 12 M H₂SO₄. Carbohydrates in the hydrolysate are subsequently quantified spectrophotometrically by MBTH (3-methyl-2-benzothiazolinone hydrazone hydrochloride) analysis. Sulfuric acid was more effective in hydrolyzing high-molecular-weight structural carbohydrates (cellulose, chitin, and alginic acid) than weak (0.09 N) hydrochloric acid. Sulfuric acid hydrolysis of dissolved and particulate samples yielded estimates of carbohydrates equal to or greater (two- to four-fold) than those resulting from dilute (0.09 N) HCl hydrolysis. In samples from the Gulf of Mexico, total dissolved carbohydrates determined after sulfuric acid hydrolysis varied from 20 to 56 μM C and from 10 to 28% of the dissolved organic carbon determined by high-temperature catalytic oxidation.     

大洋溶解铁的物质来源及其同位素示踪

铁（Fe）作为海洋初级生产所必需的微量和限制性营养元素影响着海洋生物群落结构、生态功能以及碳循环,理解溶解Fe的物质来源及其对气候变化的响应具有重要的科学意义。早期研究多强调风尘输入是维持大洋Fe循环的主要机制。近年来,随着海水Fe分析数据的积累,尤其是痕量元素及其同位素海洋生物地球化学循环研究计划（GEOTRACES）的开展,陆架沉积物和热液活动所释放Fe的贡献开始越来越受到重视。尽管如此,不同物源对开阔大洋溶解Fe的影响依然存在相当的不确定性。以海水溶解Fe的化学组分为出发点,强调有机配体对大洋Fe循环的决定性作用,综述了不同来源Fe的通量估计和第四纪大洋Fe来源的研究争议。铁同位素为理解大洋Fe的物源演变提供了新的工具。讨论了不同物源的Fe同位素特征,并提出结合沉积物的活动性Fe同位素和组分研究可能为理解过去陆架-热液活动-风尘输出与输运Fe的机制提供全新视角。     

Geochemical characteristics and isotopic reversal of natural gases in eastern Kopeh-Dagh,NE Iran

Natural gas samples from two gas fields located in Eastern Kopeh-Dagh area were analyzed for molecular and stable isotope compositions. The gaseous hydrocarbons in both Lower Cretaceous clastic reservoir and Upper Jurassic carbonate reservoir are coal-type gases mainly derived from type III kerogen, however enriched δD values of methane implies presence of type II kerogen related material in the source rock. In comparison Upper Jurassic carbonate reservoir gases show higher dryness coefficient resulted through TSR, while presence of C₁C₅ gases in Lower Cretaceous clastic reservoir exhibit no TSR phenomenon. Carbon isotopic values indicate gas to gas cracking and TSR occurrence in the Upper Jurassic carbonate reservoir, as the result of elevated temperature experienced, prior to the following uplifts in last 33–37 million years. The δ¹³C of carbon dioxide and δ³⁴S of hydrogen sulfide in Upper Jurassic carbonate reservoir do not primarily reflect TSR, as uplift related carbonate rock dissolution by acidic gases and reaction/precipitation of light H₂S have changed these values severely. Gaseous hydrocarbons in both reservoirs exhibit enrichment in C₂ gas member, with the carbonate reservoir having higher values resulted through mixing with highly-mature-completely-reversed shale gases. It is likely that the uplifts have lifted off the pressure on shale gases, therefore facilitated the migration of the gases into overlying horizons. However it appears that the released gases during the first major uplift (33–37 million years ago) have migrated to both reservoirs, while the second migrated gases have only mixed with Upper Jurassic carbonate reservoir gases. The studied data suggesting that economic accumulations of natural gas/shale gases deeper than Upper Jurassic carbonate reservoir would be unlikely.     

Stocks and dynamics of dissolved and particulate organic matter in the southern Ross Sea, Antarctica

Dissolved and particulate organic matter was measured during six cruises to the southern Ross Sea. The cruises were conducted during late austral winter to autumn from 1994 to 1997 and included coverage of various stages of the seasonal phytoplankton bloom. The data from the various years are compiled into a representative seasonal cycle in order to assess general patterns of dissolved organic matter (DOM) and particulate organic matter (POM) dynamics in the southern Ross Sea. Dissolved organic carbon (DOC) and particulate organic carbon (POC) were at background concentrations of approximately 42 and 3 μM C, respectively, during the late winter conditions in October. As the spring phytoplankton bloom progressed, organic matter increased, and by January DOC and POC reached as high as 30 and 107 μM C, respectively, in excess of initial wintertime conditions. Stocks and concentrations of DOC and POC returned to near background values by autumn (April). Approximately 90% of the accumulated organic matter was partitioned into POM, with modest net accumulation of DOM stocks despite large net organic matter production and the dominance of Phaeocystis antarctica. Changes in NO₃ concentration from wintertime values were used to calculate the equivalent biological drawdown of dissolved inorganic carbon (DIC_equiv). The fraction of DIC_equiv drawdown resulting in net DOC production was relatively constant (ca. 11%), despite large temporal and spatial variability in DIC_equiv drawdown. The C : N (molar ratio) of the seasonally produced DOM had a geometric mean of 6.2 and was nitrogen-rich compared to background DOM. The DOM stocks that accumulate in excess of deep refractory background stocks are often referred to as “semi-labile” DOM. The “semi-labile” pool in the Ross Sea turns over on timescales of about 6 months. As a result of the modest net DOM production and its lability, the role DOM plays in export to the deep sea is small in this region.     

Cycling of dissolved and particulate nitrogen and carbon in the Framvaren Fjord, Norway: stable isotopic variations

The reaction pathways of nitrogen and carbon in the Framvaren Fjord (Norway) were studied through stable isotope analysis (δ¹⁵N and δ¹³C) of dissolved inorganic and particulate organic matter (POM). The variations in the isotopic compositions of the various C and N pools within the water column were use to evaluate the historical deposition of material to the sediments. The high δ¹⁵N-NH₄⁺ at the O₂/H₂S interface, as a consequence of microbial uptake between 19 and 25 m, results in extremely depleted δ¹⁵N-particulate nitrogen (PN) of approximately 1‰ within the particulate maximum at approximately 19 m. The carbon isotopic distribution of dissolved inorganic carbon (DIC) and particulate organic carbon (POC) within the interface suggests that the distinct microbial flora (Chromatium sp. and Chlorobium sp.) fractionate inorganic carbon to different degrees. The extremely light δ¹³C-POC within the interface (−31‰) appears to be a result of carbon uptake by Chromatium sp. while δ¹³C-POC of −12‰ is more indicative of Chlorobium sp. Nitrogen isotopic mass balance calculations suggested that approximately 75% of the material sinking to the sediments was derived from the dense particulate maximum between 19 and 25 m. The sediment distribution of nitrogen isotopes varied from 2‰ at the surface to approximately 6‰ at 30 cm. The nitrogen isotopic variations with depth may be an indicator of the depth or position of the O₂/H₂S interface in the fjord. Low sediment δ¹⁵N indicated that the interface was within the photic zone of the water column, while more enriched values suggested that the interface was lower in the water column potentially allowing for less fractionation during biological incorporation of dissolved inorganic nitrogen. Results indicate that the dense layers of photo-autotrophic bacteria in the upper water column impart unique carbon and nitrogen isotopic signals that help follow processes within the water column and deposition to the sediments.     

Variations in the quantity and composition of seston from an estuary in southern Chile on different temporal scales

Estuaries are characterised by highly variable environmental conditions largely driven by tidal and atmospheric forces. This study investigates variation in the physical environment and the composition of the seston on various temporal scales in the Quempillén estuary, southern Chile. The water column was sampled throughout the tidal cycle at various times of the year. Total particulate matter, particulate inorganic matter, particulate organic matter, particle numbers, total particle volume, proximate biochemical composition and energy content of the seston, chlorophyll a and chloropigments were routinely measured. In each of the months in which sampling took place, two or three tidal cycles were examined. The information not only helps to explain the dynamics of the estuary, but is essential for an understanding of the physiology and ecology of the suspension-feeders which exploit the seston as a food source, the most dominant being the gastropod Crepipatella dilatata. Temperature and salinity were generally highest during summer, but seston quality, defined by energy content and biochemical composition (lipid, protein and carbohydrate) was higher at the end of winter and during spring. Chlorophyll a values were greatest in late spring (November). Many of the variables studied changed frequently according to the phase of the tidal cycle, and in several cases significant differences were observed among tidal cycles from the same month of the same year. In general the variables measured did not exhibit consistent patterns linked to the tidal cycle, possibly because any such patterns were masked by atmospheric conditions (wind and rain) that dominate the region and greatly influence the estuary. The quantity and quality of the seston available to suspension-feeders is largely determined by these atmospheric forces, which cause an influx of terrigenous material from adjacent areas and also resuspend bottom sediment. These effects are magnified by the shallowness of the estuary (<2 m depth). The food supply for C. dilatata and other suspension-feeders therefore varies on temporal scales varying from hourly (tidal cycle) to daily/weekly (atmospheric forces) to monthly (seasonal influences), but inhibition of feeding by low salinity sometimes limits the ability of C. dilatata to exploit fully the available organic matter.     

Distribution and morphology of mud volcanoes and other fluid flow-related lake-bed structures in Lake Baikal, Russia

New high-resolution multibeam bathymetry data recorded in 2009 in the deepest lake in the World, Lake Baikal, Siberia, enabled a better understanding of the morphology of ten known lake-bed structures—the Bolshoy, Malenki, Malyutka and Stari mud volcanoes in the South Baikal Basin, the K1–4 structures in the Selenga delta, and the Novosibirsk and St. Petersburg structures in the Central Baikal Basin—and also the discovery of 29 new lake-bed structures. These new structures are the S1, Tolstiy, mTSG and S2 in the South Baikal Basin, the P1–P4, P6–P19 and K5–K8 in the Selenga delta accommodation zone, and the C1, C3 and C4 edifices in the Central Baikal Basin. In all, 39 positive relief structures were identified and their large-scale distribution mapped. Based on their typical shape, the observation of high-reflectivity areas on side-scan sonar data records, and evidence of feeder channels on subsurface data, these structures can be classified as mud volcanoes. This has already been confirmed in other publications for the Bolshoy, Malenki and K2 structures, by the recovery of mud breccias in sediment cores. Most structures occur on or near faults and have orientations parallel with the major faults and main stress orientations in the basins, suggesting a strong structural control on the formation of the mud volcanoes. Their slopes are generally steeper than 5°, consistent with interpretation as mud cones formed by high-viscosity, stiff mud plugs. Only few structures appear to be characterised by a crater, in which case this apparent crater seems to be formed by the coalescence of several single cones, leaving a depression in the centre. Some structures have a moat, which has probably an erosional origin. Furthermore, three depressions have been found, named P5, P20 and C2, which are suggested to be pockmarks.