Vertical transport of steroid alcohols and ketones measured in a sediment trap experiment in the equatorial Atlantic Ocean

The vertical flux and free steroid alcohol (sterol) and ketone composition of particulate material was determined using sediment traps deployed at 389, 988, 3755 and 5068 m at a station in the equatorial North Atlantic, PARFLUX E. Cholest-5-en-3β-ol (cholesterol) was found to be the dominant sterol in all the traps. This compound had a maximum flux at 988 m, accounting for more than 90% of the sterols at this depth. Inputs from mesopelagic Zooplankton populations living in or migrating to depths between the 389 and 988 m traps appear to be responsible for this distribution. The deeper two traps exhibited an increased flux of phytosterols relative to cholesterol, probably due to (a) the incorporation of labile phytoplankton remains in fecal pellets and rapid transport into the deep sea and (b) differential dissolution of heterogeneous large particles. A maximum of 5–22% of the sterols produced in the euphotic zone were present in the 389 m trap. This value drops to less than 1% for the 5068 m trap, 200 m above the sediment surface.In general steroid ketone fluxes gradually decreased with depth. Δ4-Stenones were found in greater abundance than their saturated counterparts. Cholest-4-en-3-one was the major steroid ketone detected in all the traps. A five-fold increase with depth in the cholest-4-en-3-one to cholesterol ratio is most likely due to microbial oxidation of sterols to steroid ketones, or higher Δ4-stenone inputs relative to sterols from organisms.     

Sterol geochemistry of sediments from the western North Atlantic Ocean and adjacent coastal areas

Core sections from coastal bay, continental slope, and continental rise surface sediments of the western North Atlantic were analyzed for sterols. Changing rate or type of sediment input, bioturbation, and chemical conversion appear to be processes important in controlling the distribution of sterols in these sediments. Comparisons of individual sterol distributions and variations in the ratio of Soxhlet-extractable to non-extractable saponified sterols indicate that for the western North Atlantic, the extent to which each process is dominant varies with proximity to shore. Evidence is presented to show that sterols in the deep sea may be at least partially terrigenous in origin and not all biogenically derived in the surface waters. These sterols, and by analogy other labile organic compounds, may serve as a source of carbon for benthic organism metabolism.     

Sterols in interstitial waters of marine sediments

In order to attempt to elucidate the nature of biogeochemical processes occurring at the water-sediment interface, sterols have been analysed in near bottom sea and interstitial waters collected in the eastern and western intertropical Atlantic ocean. Free and esterified sterol concentrations range from 0.2 to 82 μg l^?1 and are much higher than those found in overlying sea water, which range from 0.2 to 1.7 μg l^?1 for the dissolved fraction and from 0.01 to 0.07 μg l^?1 for the particulate fraction. Cholest-5-en-3β-ol and 24-ethylcholest-5-en-3β-ol are the dominant sterols in sea and interstitial waters. The variability encountered for the relative importance of minor sterols such as 24-methylcholesta-5,24(28)-dien-3β-ol and stanols, 5α-cholest-22(E)-en-3β-ol, 5α-cholestan-3β-ol and 24-ethyl-5α-cholestan-3β-ol in interstitial water and their variation with depth is discussed in terms of diversity of inputs and bacterial activity. For sediments cored off the Mauritanian coast, a productive area characterized by an intense upwelling, the chemical signatures observed in interstitial water through stanol/stenol ratios occur at levels of very high heterotrophic aerobic bacterial biomass estimations. The study of the sterol composition of interstitial water could constitute a valuable tool in appreciating the intensity of chemical and biological processes occurring in the first few metres of recent marine sediments.     

Stenols and stanols in the oxic and anoxic waters of the Black Sea

Water samples collected from a slope station and two deep stations in the western basin of the Black Sea were analyzed for stenols and stanols by glass capillary gas chromatography. These results were used in conjuction with hydrographic, particulate organic carbon, and chlorophyll a data to better understand sterol sources and their transport and transformation mechanisms in anoxic basins.The total free sterol concentrations found in the surface waters were 450–500 ng/l dropping rapidly to values well below 100 ng/l at depths below the $\text{O}{}_2\text{H}{}_2\text{S}$ interface. In the upper 200 m of the water column a strong association of sterols with particulate matter is suggested. Structural elucidation by a gas chromatograph-mass spectrometer-computer system revealed the presence of at least sixteen different stenols and stanols in the surface waters of the Black Sea. Cholesterol, 24-methylenecholesterol and 24-methylcholesta-5,22-dien-3β-ol were the major sterols in the surface waters. Cholesterol and 24-ethylcholesterol both exhibited a subsurface maximum at the $\text{O}{}_2\text{H}{}_2\text{S}$ interface. In the anoxic deep waters (200–2000 m) only cholesterol and 24-ethylcholesterol were found. Two stenols were found that have not been reported in seawater: a C₂₆ stenol with a saturated C₇H₁₅ side chain (presumably 24-norcholesterol) and 24-ketocholesterol. At least six 5α-stanols could be identified in the surface samples, each of them comprising about 10–20% of the concentration of the corresponding Δ5-stenol. From these comparatively high surface values the stanol concentrations drop rapidly to values near zero at the $\text{O}{}_2\text{H}{}_2\text{S}$ interface. Except for very low concentrations of 5α-cholestanol (< 4ng/l) no other stanols could be detected in the anoxic zone.From this data it appears that no detectable stenol → stanol conversion is occurring at the $\text{O}{}_2\text{H}{}_2\text{S}$ interface or in the deep anoxic waters of the Black Sea.     

Quantitative measurement of the sea ice diatom biomarker IP25 and sterols in Arctic sea ice and underlying sediments: Further considerations for palaeo sea ice reconstruction

The lipid content of sea ice samples collected in 2011 and 2012 from Resolute Passage in the Canadian Arctic Archipelago was measured and compared with related samples obtained from the Amundsen Gulf in 2008. The highly branched isoprenoid (HBI) sea ice biomarker, IP₂₅, was found in sea ice samples from each study, consistent with its formation by diatoms during the spring bloom. Our analysis also revealed the occurrence of a number of sterols in Arctic sea ice and these were rigorously identified and quantified for the first time. Concentrations of IP₂₅ and sterols exhibited some variability between sampling studies, with somewhat higher values in samples from Resolute in 2012 than for the other two datasets, consistent with a general increase in biomass; however, major differences in biomarker concentration between sampling studies were not observed. An estimate of the proportion of Arctic sea ice diatoms that produce IP₂₅ (ca. 1–5%) was obtained by comparison of the concentration of IP₂₅ in the samples with those in laboratory cultures of known HBI-producing diatoms and cell enumeration in selected sea ice samples. The estimate is similar to the proportion of Haslea spp. in the same samples, providing further support to the suggestion that at least some species of the Haslea genus may be responsible for the biosynthesis of IP₂₅ and related HBI diatom lipids in Arctic sea ice and that IP₂₅ is made by a relatively small proportion of sea ice diatoms. In contrast, median sterol/IP₂₅ values were all substantially higher than those in cultures of HBI-producing diatoms, suggesting that sterols are made by the majority of sea ice diatoms. The sterol/IP₂₅ ratio was quite variable between locations and samples, likely as a result of differences in diatom assemblage; however, a comparison of individual and median sterol/IP₂₅ values in sea ice with those from surface sediments from different Arctic regions demonstrated that sterols from sea ice diatoms may, in some cases, have a significant impact on the sedimentary budget. This should be considered carefully for quantitative estimates of palaeo sea ice reconstruction using methods such as the PIP₂₅ index, which are based on the relative concentrations of IP₂₅ and sterols in Arctic marine sediment cores.     

Free,esterified and residual bound sterols in Black Sea Unit I sediments

Detailed compositional data for the sterols isolated from a surface, Unit I, sediment from the Black Sea are reported. A procedure based on digitonin precipitation has been used to separate the more abundant free sterols from those occurring in esterified forms. Saponification of the solvent extracted sediment residue liberated only a small quantity of residual bound sterols in contrast to studies of other sediments. 4-Methylsterols are much more abundant than 4-desmethylsterols in both the free and esterified sterol fractions which we attribute to a major dinoflagellate input, as in deeper Unit II sediment. The desmethylsterol fraction appears to derive from a variety of sources including dinoflagellates, coccolithophores, diatoms, terrigenous detritus and perhaps invertebrates. 5α(H)-Stanols are particularly abundant in the free sterol fraction. An analysis of the stanol/stenol ratios suggests that the 4-desmethyl-5α(H)-stanols are the result of specific microbial reductions of Δ⁵-sterols and/or the reflection of a contribution of stanol containing source organisms.     

Free and bound lipids in recent (1835–1987) sediments from Santa Barbara Basin

In order to study the first steps of incorporation of lipids in recent organic-rich sediments into free and bound fractions, we have selected the Santa Barbara Basin, off California. This basin with a maximum of 590 m water depth is characterized by high phytoplankton production in surface waters and a low oxygen content in bottom waters. Sediments show the following features: high sedimentation rate ≈ 4 mm/yr, no bioturbation, and development of a bacterial mat community at the surface with predominance of sulphur-oxidizing bacteria trapping particles, thus preventing re-distribution of sediment, which permit a unique observations of organic sedimentation on a new few years basis.A sediment core has been divided into 2 cm thick slices corresponding to a time resolution of ≈5 years, from 1835 up to 1987. Samples have been analyzed using a multi-parameter approach, such as for plankton species identification, carbon stable isotope ratios and, as reported here, for lipid organic tracers. Organic tracers have been analyzed in the sterol and fatty series for both free and bound compounds by gas chromatography and gas chromatography/mass spectrometry.The incorporation processes of sterols with depth appear different for free and bound compounds. Total free sterol concentrations show high values in surface sediments (≈ 100 μg/g dry sediment), rapidly decrease up to ≈ 10 cm depth and remain at a constant value of 30–40 μg/g. Total bound sterol concentrations show low values in surface sediment (13.6 μg/g), and vary irregularly with depth up to a value of 55 μg/g at 7.3 m, and then remain constant at 25–26 μg/g.Profiles of evolution with depth of free C₂₇, C₂₈ sterols show a regular decrease, whereas C₂₉ sterols show an irregular decrease with anomalies at 7.3 cm (approximately age: 1977–1978) and at 14.1 cm (1962–1964). Profiles of bound compounds are rather different, very regular for C₂₈ sterols, irregular with oscillations for C₂₇ and C₂₉ sterols at 7.3, 12.2 and 18.0 cm (1954–1956), suggesting a different mode of incorporation and probably different inputs for C₂₇, C₂₉ and C₂₈ sterols.The study of the kinetics of degradation of sterols between surface (1987) and 10.5 cm (1968–1972) shows that C₂₇ compounds are degraded at a slight higher rate (0.53 μg/μg of initial C₂₇ concentration/ year) than are C₂₈ and C₂₉ compounds (0.047 μg/μg of initial concentration/year). An intermediate value is found for brassicasterol: 0.049 μg/μg/year.     

Sterols as source indicators of organic materials in sediments

The sterol contents of plankton and sediment samples have been determined. Cholesterol, 22-dehydrocholesterol, brassicasterol, campesterol, 24-methylenecholesterol, stigmasterol, and β-sitosterol are the major sterols in these samples. Systematic variations have been observed in the compositions of the sterols from bay and Gulf of Mexico plankton and from sediments collected in the mouth of the Aransas River, Capano Bay, Aransas Bay, Corpus Christi Bay and the Gulf near Port Aransas. The concentration of cholesterol increases as the concentration of β-sitosterol decreases in the sample sequence of river inlet sediments-bay sediments-Gulf sediments-bay and Gulf plankton. Calculations based on either the cholesterol or the β-sitosterol contents of the sterol fractions of the fresh water sediments and the Gulf plankton and sediments suggest that 34% of the sterols in the Gulf sediments are derived from terrigenous sources.     

The effects of sea salts on the forms of nitrogen released from estuarine and freshwater sediments: Does ion pairing affect ammonium flux?

In sediments with oxidized surface layers, the percentage of mineralized nitrogen that is nitrified/denitrified, compared with that released directly as ammonium, appears to be affected by the presence of sea salts. In estuarine systems, a significant portion of the nitrogen is released as ammonium, whereas in freshwater systems, most of the mineralized nitrogen is often released from the sediments as nitrogen gas. We hypothesized that this discrepancy is caused by differential competition between physical diffusion and nitrification/denitrification in the two systems. The vertical migration (by Fickian diffusion) of ammonium out of the oxic layer may be hindered by cation exchange (or sorption) interactions with sediment particles to a greater extent in fresh water than in estuarine systems. The resulting relatively long residence time, and potentially high levels of particle-bound ammonium in the freshwater sediments, would favor nitrification as the major ammonium removal process. By contrast, ion pair formation of ammonium with seawater anions and blockage of sediment cation exchange sites with seawater cations may allow a sizable fraction of the ammonium to diffuse out of estuarine sediments before it is nitrified. A salt effect, consistent with this hypothesis, has been demonstrated in experimental systems by changing the ionic composition of water flowing above intact cores of freshwater and estuarine sediments. Steady-state ammonium release from Lake Michigan sediments was substantially enhanced in the presence of 30% seawater over that in the presence of lake water alone. Likewise, steady-state ammonium release, from Ochlockonee River and Bay sediments (Florida) and from Toms River and Barnegat Bay sediments (New Jersey), was usually higher in the presence of diluted synthetic seawater than it was in the presence of fresh water.     

海洋天然气水合物元素地球化学异常的实验研究

海洋天然气水合物在生成过程中会引起周围沉积物孔隙水中元素地球化学异常,这些异常是指示天然气水合物存在的重要标志。在自制的实验装置上,模拟了海洋天然气水合物的生成过程,对海水中各离子浓度的变化进行了初步研究。结果表明：在不同的反应条件下,水合物的生成对各离子浓度变化的影响不同。压力越大,耗气量越大,生成水合物的量就大、纯度高,其排盐效应也较强,导致海水溶液中离子浓度的增高,而水合物中离子含量却呈降低趋势。     

全球海水剖面Fe同位素组成的不均一性及其影响因素

全球海水剖面Fe同位素组成存在显著不均一性.对大西洋洋中脊、大西洋近海岸带、东太平洋和西太平洋弧后扩张中心多个站位的海水剖面溶解Fe浓度和Fe同位素组成进行了综合分析,得出以下主要认识:（1）不同区域的海水剖面溶解Fe浓度和Fe同位素组成呈现不同的变化特征,海水Fe同位素的变化趋势与海水溶解氧浓度变化一致,而与海水溶解Fe浓度呈镜像变化关系;（2）不同深度的海水溶解Fe浓度和Fe同位素组成特征的主要控制因素不同.表层海水受到大气降尘、生物作用影响呈现富重Fe同位素特征,受河流的影响Fe同位素组成偏轻;深层海水主要受到深海沉积和海底热液活动的影响,其中沉积物中的非还原溶解Fe导致海水富集重Fe同位素,而受洋中脊热液流体影响的深部海水显著富集轻Fe同位素;（3）将目前已知海底热液溶解Fe通量最小值（0.5 Gmol/a）作为全球大洋的热液溶解Fe通量,利用不同来源的溶解Fe同位素与其通量间的关系估算海底热液对海洋的Fe循环的贡献为~5.5%.由于海底热液流体的Fe通量可能远大于0.5 Gmol/a,因此,海底热液活动对海洋溶解Fe的贡献可能远超过前人的估算结果（6.0%）.      

Occurrence of Different Forms and Implications of Compound Specific Sterols in Continental Sediments of the Northeast South China Sea

The South China Sea(SCS) is one of the most productive and accumulative marginal shelves of organic carbon in the world. To expound the transformation and preservation of organic carbon in the Northeast SCS, where abundant oil and gas resources have been reported, compound specific sterols in free(FR), base hydrolytic(BH), and acid hydrolytic(AH) forms were analyzed in surface and columnar sediments in May, 2016. The results showed that the total contents of sterols detected ranged from 0.15 to 3.74 ppm dry weight in the surface sediments, and gradually decreased from 3.41 to0.17 ppm dry weight from surface to deep sediments, in which cholesterol(27~(△5)) was the most abundant component. Sterols mainly existed in the BH form(54.51%-74.20%), followed by the FR form(25.50%-45.49%) and then the AH form(0-3.77%) in turn, in the surface sediments. BH and FR sterols accounted for 0-49.08% and 50.92%-100% in the columnar sediments, while AH sterols were undetectable. The contents of specific sterols indicated that, the primary source of marine organic carbon was about 5 times as much as that from terrestrial input. More and more FR sterols transformed into BH sterols with increasing sedimentary depth, and BH sterols absolutely dominated in sediment depths under 25 cm. The forms of Sterols C27 were maintained at a relative consistence state, but Sterols C28 to C30 degraded gradually during the sedimentation process. It was suggested that the stability of sterols, based on the chemical structures, might be the primary factor controlling their degradation and preservation in deeper sediments. These results would help to understand the organic carbon(OC) transformation in a hydrate formation area in a marginal sea.     

Sources of neutral lipids in a temperate intertidal sediment

The compositions of sterol, alcohol and ketone fractions from an oxic intertidal surface sediment from Corner Inlet. Victoria, Australia, have been examined by capillary gas chromatographymass spectrometry and related to the lipids of diatoms cultured from the sediment and to lipids of the sea-grass Zostera muelleri. Of the more than thirty sterols in the sediment most appear to derive from diatoms, including the major sterol 24-methylcholesta-5.22E-dien-3β-ol. Small amounts of 24-ethylcholesterol probably derive from Zostera, with a minor diatom contribution. 5α-stanols, both fully saturated and with a side-chain double bond, represented ca. 14% of the total sterols: a significant proportion of these are probably derived from marine invertebrates. These organisms also contribute C₂₆ sterols. most of the cholesterol and possibly small amounts of Δ-sterols. The data suggest that in situ biohydrogenation of stenols was not a major process in sterol transformation in the surface oxic sediment. Alcohols ranged from C₁₂ to C₃₀ and showed an unusual abundance of unsaturated components with Δ⁹-16:1 being the major constituent. The long-chain alcohols probably originate largely from Zostera but the shorter-chain. C₁₂-C₂₀. alcohols are at least partly derived from wax esters of unknown origin. Diatoms do not contribute significant amounts of alcohols. Ketones were not major constituents of the sediment and consisted mainly of 6.10.14-trimethylpentadecan-2-one and a series of n-alkan-2-ones ranging from C₁₆ to C₃₃. The latter showed a similar distribution to that of the n-alkanes but the correspondence was not sufficient to substantiate a product-precursor relationship. Very long-chain C₃- C₃₉ unsaturated methyl and ethyl ketones, which may originate from the marine unicellular alga Emiliania huxleyi. were present in low concentration.     

Time-dependent modeling of the Baltic entrance area. 1. Quantification of circulation and residence times in the Kattegat and the Straits of the Baltic sill

A prognostic model for the estuarine circulation in the Baltic entrance area is described. The model is based on the work by Stigebrandt (1983) and is built of a number of flow-regulating physical processes and forced by oceanic sea level, local meteorological conditions, and freshwater supply to the Baltic. It resolves the horizontal variations by dividing the entrance area into 7 sub-basins. The vertical stratification in each sub-basin evolves with time due to mixing, diffusion, and water exchange with adjacent basins. Instead of using a fixed vertical grid, the stratification is described by a variable number of layers created by inflowing water and by a pycnocline retreat near the surface. The model is a highly cost-effective tool compared to high-resolution 3D-models since computations are 10⁵–10⁶ times faster. Still, the model reproduces the stratification on time-scales longer than a few days as verified by comparison with observed time-series. The magnitude of the simulated average estuarine circulation conforms well to independent estimates of the water exchange. The model is used to quantify the temporal and horizontal variability of circulation, mixing, and diffusion. Long-term average rate of work against the buoyancy forces by entrainment and diffusion is calculated for each sub-basin. The highest rates of work against the buoyancy forces by diffusion are found in the northern Kattegat and in the Fehmarn Belt while the lowest rate is found in the Öresund. The total mixing in terms of transformation of water masses is also quantified. The average residence times for surface and deep water are estimated for each subbasin. Residence times longer than 1 mo are found in Fehmarn Belt and in the deep water of southern Kattegat. In other parts of Kattegat and the Samsø Belt the residence times are 1 to 2 wk for surface water and 2 to 3 wk for deep water. The age of the water is defined as the time spent since a particular water mass was in contact with either the sea surface or with the vertical model boundaries has been estimated. By comparing the age distribution in the Kattegat with observations of oxygen concentration, it is concluded that the variability of the ventilation of deeper layers is of less importance to the occurrence of low oxygen concentrations compared to other factors such as interannual variability in primary production.     

东濮凹陷下第三系沙河街组盐类沉积模式新见

文中认为在东濮凹陷中自沙河街组四段沉积中晚期开始,海水随着海面升降,间歇性地进入由北东向的兰聊断裂和长垣断裂构成的古河谷。高位期,海水以相对暂时性抬高的形式,淹没本区,致使凹陷南部成为向东南或南开口的河口湾,构成盐湖沉积的先期沉积环境,到低位期,海水退出凹陷区,部分海水因 受东西向同沉积走滑断裂（高平集-习城集一线）高地的阻隔而潴留,局限在高平集-习城集断层至文明寨-范县断层的同沉积构造凹陷,潴留海水蒸发、浓缩,形成盐类。在较深的凹地,受陆源淡水的影响较小,卤水浓度相对较高,那里依次沉积了具有深水沉积特点的碳酸盐岩、石膏、石盐等;而在水体较浅的凹地,（如砂砰、泥坪环境）,那里易受季节性洪水影响,卤水淡化,沉积了具有明显浅水特征的灰质泥岩、泥膏岩等。     

青海湖沉积物中的甾醇及其演化

Ｃ_２７，Ｃ_２８和Ｃ_２９甾醇（△５.２２，△２２，△５和△５.２４（２８）和５α－甾烷醇）在青海湖三孔近代沉积物（ＱＨ，ＱＥ和ＱＯ）中被检出。其中以Ｃ_２９甾醇占优势。在ＱＥ和ＱＧ孔沉积物中还检出了低浓度的三个Ｃ_３０甾醇（４α，２３，２４－三甲基－５α－胆甾－２２Ｅ－烯醇（甲藻甾醇），４α－甲基－２４－乙基－５α－胆甾－２２Ｅ－烯醇和４α－甲基－２４－乙基－５α－胆甾烷醇］。在ＱＨ和ＱＧ孔上部层段沉积物中，Ｃ_２７，Ｃ_２９.饱和的和不饱和的甾醇的碳数分布的平行性，甾烷醇/△５－甾醇及△２２－/△５.２２－甾醇的比值随沉积物埋深而增加提供了甾酸氢化作用的间接证据。青海湖沉积物中的甾醇主要来自湖区丰富的高等植物和湖中的藻类等。在ＱＧ孔８０～１００ｃｍ和１２０～１４０ｃｍ层段沉积物中，５ａ－胆甾烷醇浓度迅速增加可能反映特殊的生物（介形类）对该二层段沉积物中高浓度的胆甾烷醇的贡献。     

Occurrence of gorgosterol in diatoms of the genus Delphineis

The presence of the C₃₀ sterol gorgosterol (22,23-methylene-23,24-dimethylcholest-5-en-3ß-ol) and its analogues in some marine and freshwater environments is generally associated with invertebrate animals or dinoflagellates since there have been no reports of them in other microalgal classes. Here we show that two unialgal cultures of different species of the marine diatom Delphineis contain gorgosterol in addition to sterols more commonly found in diatoms. Our findings suggest that some reports of gorgosterol in seawater and marine sediments may well have an origin, at least in part, from diatoms.     

深海甲烷电化学原位长期监测技术及其在海洋环境调查和天然气水合物勘探中的意义

深海溶解甲烷浓度数据连续获取的方法技术,对于海洋环境和天然气水合物开发过程中甲烷扩散作用及通量的动态监测,具有重要的科学意义和实际应用价值。本文较详细地介绍了依据"海水脱气、气体样品定量输入、电化学高精度检测"技术思路,采用"增压排液整机系统控制的海水循环、减压稳流、气液分离、烃类组分高精度检测技术改进"方法,研发"深海甲烷电化学原位长期监测技术"的关键环节和技术方法。结合原位传感器在胶州湾港口为期94天底水长期监测实验获取的数据成果,对原位传感器的技术性能、数据质量、地质效果进行了研究评价。结果表明:(1)原位传感器量程甲烷指标达到0.01～10 000 nmol/L,灵敏度达到0.01 nmol/L,对烃类组分检测具有较好的稳定性和选择性;(2)监测水域溶解甲烷数值范围19.01～106.87 nmol/L,正常甲烷背景32.41 nmol/L,局部异常甲烷背景80.60 nmol/L,资料显示异常与污水排放过程对海水环境污染有关;(3)实测甲烷数据成果地球化学特征与胶州湾海域海水环境以往调查研究成果符合,证明了实测数据的客观性和科学性;(4)海试监测试验成果证明,原位传感器测试性能可靠、结构设计合理、设计思路科学,基本具备了海洋科学调查中对海水甲烷浓度数据获取的能力,在未来海洋天然气水合物开发过程中对甲烷扩散作用的动态监测及深海甲烷浓度通量的长期监测中,具有实际应用价值和科学意义。     

近海油气藏渗漏烃的检测方法综述

主要总结了海域油气藏渗漏烃的航空遥感和地球化学检测方法.遥感测量可以从宏观上圈定海面油膜的分布范围,是海上油气藏勘探前期常用的廉价方法;海底沉积物取芯测量和海水嗅探器现场分析是海域油气藏渗漏烃地球化学检测的主要手段,海水样品的脱气处理是海水介质中渗漏烃地球化学检测的关键环节;海水和海底沉积物取样设备与脱气技术的不断完善,为海域油气藏渗漏烃的检测提供了基本保障;目前,底层水采样分析与海底沉积物取芯分析已成为一种有效且相对经济的海域油气藏渗漏烃检测技术组合,与一些地球物理方法结合应用,可有效地圈定海底下方渗漏源的位置.     

Paleoceanographic changes of surface and deep water based on oxygen and carbon isotope records during the last 130 kyr identified in MD179 cores,off Joetsu,Japan Sea

We reconstructed the paleoenvironmental history of surface and deep water over the last 130 kyr from oxygen and carbon isotope ratios of planktonic and benthic foraminifera in two cores (MD179-3312 and MD179-3304) from the Joetsu Basin, eastern margin of the Japan Sea. Our data showed that paleoceanographic changes such as influx of surface currents and vertical circulation were associated with global glacial–interglacial sea level change. Surface water conditions were influenced by the influx of Tsushima Current, East China Sea coastal or off-shore waters through the Tsushima Strait during interglacial or interstadial stages, and strongly affected by freshwater input during the glacial maximum. During interglacial maximums such as Marine Isotope Stages 1 and 5e, development of well-oxygenated bottom water was indicated. A density-stratified ocean with weak ventilation was inferred from the isotopic records of benthic foraminifera during the Last Glacial Maximum. Local negative excursions in carbon isotopes during deglacial or interglacial periods may suggest the dissolution of gas hydrates or methane seep activities.