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1.
In natural gas hydrate marine settings, cold seepage of methane fluid is a widely observed phenomenon, where authigenic minerals serve as an indication of potential gas hydrate-bearing reservoirs at depth. In this study, based on the data from the site HD196 near Dongsha Island, northern continental slope of South China Sea, laboratory experiments and numerical simulation studies were conducted to investigate the biogeochemical processes of authigenic mineral formation induced by methane seepage. The bioreactor experimental results show that in response to methane flux, pH increased to 8.5 after 20 days of reaction, and Eh declined rapidly first and then remained unchanged at about 100 mV. The decrease in SO42−, HS− and HCO3− concentrations indicated the occurrence of anaerobic oxidation of methane coupled with sulfate reduction (AOM-SR). The depletion of Fe2+ implied the formation of iron-bearing minerals, e.g., iron sulfides. Carbonate minerals were also identified in the experimental phase of this study. Most iron sulfides existed as massive pieces, and in some cases as spherical or rod-shape pieces. The calcium carbonates were observed as blocky pieces. Numerical simulations were also performed to reproduce the biogeochemical reactions that occurred in the reactor experiments. Based on experimental data, kinetic parameters associated with the observed reactions were calibrated. The model simulated results are general consistent with those obtained by the experiments conducted in this study. The combination of simulation and experimental studies provided a powerful tool to investigate the biogeochemical processes in the methane leakage environment at different temporal and spatial scales. This study gave a new perspective to understand the formation of cold seep authigenic minerals in marine sediments, and was significant for future investigations on the effects of hydrate decomposition.  相似文献   

2.
Host sediments may exert a significant influence on the formation of gas hydrate reservoirs. However, this issue has been largely neglected in the literature. In this study, we investigated the types, characteristics and the depositional model of the fine-grained gas hydrate-bearing sediments in the northeastern margin of the South China Sea by integrating core visual observations and logging-while-drilling downhole logs. The gas hydrate-bearing sediments consist dominantly of muddy sediments formed in the inter-canyon ridges of the upper continental slope, including hemipelagites, debrites (mud with breccia) and fine-grained turbidites. Cold-seep carbonates and associated slumping talus, muddy breccia debrites, as well as coarse-grained turbidites, may locally occur. Four classes and six sub-classes of log facies were defined by cluster analysis. Core-log correlation indicates that gas hydrates are majorly distributed in fine-grained sediments with high resistivity and low acoustic transit time (AC) log responses, which are easily differentiated from the fine-grained background sediments of high gamma-ray (GR), high AC, and low resistivity log values, and the seep carbonates characterized by low GR, high resistivity, high density, low AC and low porosity log values. The primary host sediments consist of fine-grained hemipelagic sediments formed by deposition from the nepheloid layers of river material and from the microfossils in seawater column. Most of the hemipelagic sediments, however, might have been extensively modified by slumping and associated gravity flow processes and were re-deposited in the forms of debrites and turbidites. Locally developed seep carbonates associated with gas hydrate dissociation and leakage provided additional sources for the gravity flow sediments.  相似文献   

3.
真光层海水中普遍存在甲烷过饱和现象,尤其是天然气水合物区真光层的甲烷明显异常。由于临近海气界面,真光层过饱和甲烷与大气甲烷排放及全球温室效应密切相关。目前,对真光层海水的过饱和甲烷来源仍没有统一的认识。综合前人研究成果梳理了真光层海水过饱和甲烷的来源,归纳了真光层海水过饱和甲烷现象形成的影响因素,进一步探讨了原位微生物可能参与的甲烷代谢机制。真光层过饱和甲烷可能来源于沉积物、临近河流或原位微生物,且受区域、季节、营养盐等多种因素的影响。由于受氧气影响,真光层海水甲烷产生的代谢机制有其特殊性,目前推测微生物可能依旧利用常规的产甲烷途径,它们存在于海水微厌氧环境中,或自身形成抵抗氧气影响的能力;此外,微生物也可能选择对氧不敏感的新的产甲烷途径。因此,针对天然气水合物区真光层甲烷过饱和现象,开展甲烷的来源和代谢机制的研究,以期为天然气水合物试采与开发的环境评价提供理论支撑,并为探究海水甲烷对大气及全球气候的影响提供理论依据。  相似文献   

4.
The geochemical cycling of barium was investigated in sediments of pockmarks of the northern Congo Fan, characterized by surface and subsurface gas hydrates, chemosynthetic fauna, and authigenic carbonates. Two gravity cores retrieved from the so-called Hydrate Hole and Worm Hole pockmarks were examined using high-resolution pore-water and solid-phase analyses. The results indicate that, although gas hydrates in the study area are stable with respect to pressure and temperature, they are and have been subject to dissolution due to methane-undersaturated pore waters. The process significantly driving dissolution is the anaerobic oxidation of methane (AOM) above the shallowest hydrate-bearing sediment layer. It is suggested that episodic seep events temporarily increase the upward flux of methane, and induce hydrate formation close to the sediment surface. AOM establishes at a sediment depth where the upward flux of methane from the uppermost hydrate layer counterbalances the downward flux of seawater sulfate. After seepage ceases, AOM continues to consume methane at the sulfate/methane transition (SMT) above the hydrates, thereby driving the progressive dissolution of the hydrates “from above”. As a result the SMT migrates downward, leaving behind enrichments of authigenic barite and carbonates that typically precipitate at this biogeochemical reaction front. Calculation of the time needed to produce the observed solid-phase barium enrichments above the present-day depths of the SMT served to track the net downward migration of the SMT and to estimate the total time of hydrate dissolution in the recovered sediments. Methane fluxes were higher, and the SMT was located closer to the sediment surface in the past at both sites. Active seepage and hydrate formation are inferred to have occurred only a few thousands of years ago at the Hydrate Hole site. By contrast, AOM-driven hydrate dissolution as a consequence of an overall net decrease in upward methane flux seems to have persisted for a considerably longer time at the Worm Hole site, amounting to a few tens of thousands of years.  相似文献   

5.
 Ikaite crystals (CaCO3×6H2O) have been found at 232- to 238-cm sediment depth in R/V Polarstern core PS2460-4 from the Laptev Sea continental margin in a water depth of 204 m. δ13C values of this phase average −36.3±0.4‰ PDB (N=2), which is significantly outside the range of normal marine carbonates. The CO2 involved in the precipitation of the ikaite is most probably derived from methane, which has extremely depleted 13C isotope values. Two possible sources of methane in these sediments are: (1) methanogenesis (decomposition of organic matter under anaerobic conditions); and (2) gas hydrates, which are known to occur in the Siberian shelf regions. Received: 20 March 1996 / Revision received: 22 July 1996  相似文献   

6.
We report some main results of multidisciplinary investigations carried out within the framework of the Indian National Gas Hydrate Program in 2002–2003 in the Krishna–Godavari Basin offshore sector, east coast of India, to explore indicators of likely gas hydrate occurrence suggested by preliminary multi-channel seismic reflection data and estimates of gas hydrate stability zone thickness. Swath bathymetry data reveal new evidence of three distinct geomorphic units representing (1) a delta front incised by several narrow valleys and mass flows, (2) a deep fan in the east and (3) a WNW–ESE-trending sedimentary ridge in the south. Deep-tow digital side-scan sonar, multi-frequency chirp sonar, and sub-bottom profiler records indicate several surface and subsurface gas-escape features with a highly resolved stratification within the upper 50 m sedimentary strata. Multi-channel seismic reflection data show the presence of bottom simulating reflections of continuous to discrete character. Textural analyses of 76 gravity cores indicate that the sediments are mostly silty clay. Geochemical analyses reveal decreasing downcore pore water sulphate (SO4 2−) concentrations (28.7 to <4 mM), increasing downcore methane (CH4) concentrations (0–20 nM) and relatively high total organic carbon contents (1–2.5%), and microbial analyses a high abundance of microbes in top core sediments and a low abundance of sulphate-reducing bacteria in bottom core sediments. Methane-derived authigenic carbonates were identified in some cores. Combined with evidence of gas-escape features in association with bottom simulating reflections, the findings strongly suggest that the physicochemical conditions prevailing in the study area are highly conducive to methane generation and gas hydrate occurrence. Deep drilling from aboard the JOIDES Resolution during 2006 has indeed confirmed the presence of gas hydrate in the Krishna–Godavari Basin offshore.  相似文献   

7.
Two sites of the Deep Sea Drilling Project in contrasting geologic settings provide a basis for comparison of the geochemical conditions associated with marine gas hydrates in continental margin sediments. Site 533 is located at 3191 m water depth on a spit-like extension of the continental rise on a passive margin in the Atlantic Ocean. Site 568, at 2031 m water depth, is in upper slope sediment of an active accretionary margin in the Pacific Ocean. Both sites are characterized by high rates of sedimentation, and the organic carbon contents of these sediments generally exceed 0.5%. Anomalous seismic reflections that transgress sedimentary structures and parallel the seafloor, suggested the presence of gas hydrates at both sites, and, during coring, small samples of gas hydrate were recovered at subbottom depths of 238m (Site 533) and 404 m (Site 568). The principal gaseous components of the gas hydrates wer methane, ethane, and CO2. Residual methane in sediments at both sites usually exceeded 10 mll?1 of wet sediment. Carbon isotopic compositions of methane, CO2, and ΣCO2 followed parallel trends with depth, suggesting that methane formed mainly as a result of biological reduction of oxidized carbon. Salinity of pore waters decreased with depth, a likely result of gas hydrate formation. These geochemical characteristics define some of the conditions associated with the occurrence of gas hydrates formed by in situ processes in continental margin sediments.  相似文献   

8.
We have implemented a 2-dimensional numerical model for simulating gas hydrate and free gas accumulation in marine sediments. The starting equations are those of the conservation of the transport of momentum, energy, and mass, as well as those of the thermodynamics of methane hydrate stability and methane solubility in the pore-fluid. These constitutive equations are then integrated into a finite element in space, finite-difference in time scheme. We are then able to examine the formation and distribution of methane hydrate and free gas in a simple geologic framework, with respect to the geothermal heat flow, fluid flow, the methane in-situ production and basal flux. Three simulations are performed, leading to the build up of hydrate emplacements largely linear through time. Models act primarily as free gas accumulators and are relatively inefficient with respect to hydrate emplacements: 26–33% of formed methane are converted to hydrate. Seepage of methane across the sea-floor is negligible for fluid flow below 2. 10−11 kg/m2/s. At 5.625 10−11 kg/m2/s however, 9.7% of the formed methane seeps out of the model. Moreover, along strike variation arising in the 2-dimensional model are outlined. In the absence of focused flow, the thermodynamics of hydrate accumulation are primarily one-dimensional. However, changes in free methane compressibility (density) and methane solubility (the intrinsic dissolved methane flux) subtlety impact on the formation of a free gas zone and the distribution of the hydrate emplacements in our 2-dimensional simulations.  相似文献   

9.
Authigenic carbonates from active methane seeps offshore southwest Africa   总被引：2，自引：1，他引：1  
The southwest African continental margin is well known for occurrences of active methane-rich fluid seeps associated with seafloor pockmarks at water depths ranging broadly from the shelf to the deep basins, as well as with high gas flares in the water column, gas hydrate accumulations, diagenetic carbonate crusts and highly diverse benthic faunal communities. During the M76/3a expedition of R/V METEOR in 2008, gravity cores recovered abundant authigenic carbonate concretions from three known pockmark sites—Hydrate Hole, Worm Hole, the Regab pockmark—and two sites newly discovered during that cruise, the so-called Deep Hole and Baboon Cluster. The carbonate concretions were commonly associated with seep-benthic macrofauna and occurred within sediments bearing shallow gas hydrates. This study presents selected results from a comprehensive analysis of the mineralogy and isotope geochemistry of diagenetic carbonates sampled at these five pockmark sites. The oxygen isotope stratigraphy obtained from three cores of 2–5?m length indicates a maximum age of about 60,000–80,000?years for these sediments. The authigenic carbonates comprise mostly magnesian calcite and aragonite, associated occasionally with dolomite. Their very low carbon isotopic compositions (–61.0?<?δ13C ‰ V-PDB?<?–40.1) suggest anaerobic oxidation of methane (AOM) as the main process controlling carbonate precipitation. The oxygen isotopic signatures (+2.4?<?δ18O ‰ V-PDB?<?+6.2) lie within the range in equilibrium under present-day/interglacial to glacial conditions of bottom seawater; alternatively, the most positive δ18O values might reflect the contribution of 18O-rich water from gas hydrate decomposition. The frequent occurrence of diagenetic gypsum crystals suggests that reduced sulphur (hydrogen sulphide, pyrite) from sub-seafloor sediments has been oxidized by oxygenated bottom water. The acidity released during this process can potentially induce the dissolution of carbonate, thereby providing enough Ca2+ ions for pore solutions to reach gypsum saturation; this is thought to be promoted by the bio-irrigation and burrowing activity of benthic fauna. The δ18O–δ13C patterns identified in the authigenic carbonates are interpreted to reflect variations in the rate of AOM during the last glacial–interglacial cycle, in turn controlled by variably strong methane fluxes through the pockmarks. These results complement the conclusions of Kasten et al. in this special issue, based on authigenic barite trends at the Hydrate Hole and Worm Hole pockmarks which were interpreted to reflect spatiotemporal variations in AOM related to subsurface gas hydrate formation–decomposition.  相似文献   

10.
《Marine and Petroleum Geology》2012,29(10):1856-1869
We have implemented a 2-dimensional numerical model for simulating gas hydrate and free gas accumulation in marine sediments. The starting equations are those of the conservation of the transport of momentum, energy, and mass, as well as those of the thermodynamics of methane hydrate stability and methane solubility in the pore-fluid. These constitutive equations are then integrated into a finite element in space, finite-difference in time scheme. We are then able to examine the formation and distribution of methane hydrate and free gas in a simple geologic framework, with respect to the geothermal heat flow, fluid flow, the methane in-situ production and basal flux. Three simulations are performed, leading to the build up of hydrate emplacements largely linear through time. Models act primarily as free gas accumulators and are relatively inefficient with respect to hydrate emplacements: 26–33% of formed methane are converted to hydrate. Seepage of methane across the sea-floor is negligible for fluid flow below 2. 10−11 kg/m2/s. At 5.625 10−11 kg/m2/s however, 9.7% of the formed methane seeps out of the model. Moreover, along strike variation arising in the 2-dimensional model are outlined. In the absence of focused flow, the thermodynamics of hydrate accumulation are primarily one-dimensional. However, changes in free methane compressibility (density) and methane solubility (the intrinsic dissolved methane flux) subtlety impact on the formation of a free gas zone and the distribution of the hydrate emplacements in our 2-dimensional simulations.  相似文献   

11.
Raman spectroscopic measurements of synthetic gas hydrates in the ocean   总被引：1，自引：0，他引：1  
A Raman spectrometer extensively modified for deep ocean use was used to measure synthetic hydrates formed in an ocean environment. This was the first time hydrates formed in the ocean have been measured in situ using Raman spectroscopy. Gas hydrates were formed in situ in the Monterey Bay by pressurizing a Pyrex cell with various gas mixtures. Raman spectra were obtained for sI methane hydrate and sII methane + ethane hydrate. Gas occlusion resulting from rapid gas growth of methane hydrate was measured immediately after formation. The Raman shift for methane free gas was coincident with that of methane in the small 512 hydrate cage. The methane Raman peak widths were used to discriminate between methane in the free gas and hydrate phase. Methane + ethane sII hydrate was formed for 43 days on the seafloor. In this case, gas occlusion was not measured when the gas hydrates were allowed to form over an extended time period. Equivalent Raman spectra were obtained for the in situ and laboratory-formed sII methane + ethane hydrates, under similar p, T, and x conditions. With the Raman spectrometer operating in the ocean, seawater contributes to the Raman spectra obtained. Both the Raman bands for the sulfate ion and water were used to qualitatively determine the distribution of water phases measured (hydrate, seawater) in the Raman spectra.  相似文献   

12.
Fossil methane from the large and dynamic marine gas hydrate reservoir has the potential to influence oceanic and atmospheric carbon pools. However, natural radiocarbon (14C) measurements of gas hydrate methane have been extremely limited, and their use as a source and process indicator has not yet been systematically established. In this study, gas hydrate-bound and dissolved methane recovered from six geologically and geographically distinct high-gas-flux cold seeps was found to be 98 to 100% fossil based on its 14C content. Given this prevalence of fossil methane and the small contribution of gas hydrate (≤ 1%) to the present-day atmospheric methane flux, non-fossil contributions of gas hydrate methane to the atmosphere are not likely to be quantitatively significant. This conclusion is consistent with contemporary atmospheric methane budget calculations.In combination with δ13C- and δD-methane measurements, we also determine the extent to which the low, but detectable, amounts of 14C (~ 1–2% modern carbon, pMC) in methane from two cold seeps might reflect in situ production from near-seafloor sediment organic carbon (SOC). A 14C mass balance approach using fossil methane and 14C-enriched SOC suggests that as much as 8 to 29% of hydrate-associated methane carbon may originate from SOC contained within the upper 6 m of sediment. These findings validate the assumption of a predominantly fossil carbon source for marine gas hydrate, but also indicate that structural gas hydrate from at least certain cold seeps contains a component of methane produced during decomposition of non-fossil organic matter in near-surface sediment.  相似文献   

13.
Pockmarks are observed worldwide along the continental margins and are inferred to be indicators of fluid expulsion. In the present study, we have analysed multibeam bathymetry and 2D/3D seismic data from the south-western Barents Sea, in relation to gas hydrate stability field and sediment type, to examine pockmark genesis. Seismic attributes of the sediments at and beneath the seafloor have been analysed to study the factors related to pockmark formation. The seabed depths in the study area are just outside the methane hydrate stability field, but the presence of higher order hydrocarbon gases such as ethane and/or propane in the expelled fluids may cause localised gas hydrate formation. The selective occurrence of pockmarks in regions of specific seabed sediment types indicates that their formation is more closely related to the type of seabed sediment than the source path of fluid venting such as faults. The presence of high acoustic backscatter amplitudes at the centre of the pockmarks indicates harder/coarser sediments, likely linked to removal of soft material. The pockmarks show high seismic reflection amplitudes along their fringes indicating deposition of carbonates precipitated from upwelling fluids. High seismic amplitude gas anomalies underlying the region away from the pockmarks indicate active fluid flow from hydrocarbon source rocks beneath, which is blocked by overlying less permeable formations. In areas of consolidated sediments, the upward flow is limited to open fault locations, while soft sediment areas allow diffused flow of fluids and hence formation of pockmarks over a wider region, through removal of fine-grained material.  相似文献   

14.
Experiments with a set of electrolyte solutions have been carried out to investigate the effects of pore water composition changes on the stability conditions of methane hydrate in marine sediments. The results reveal that (1) SO42− and Cl− concentration changes can affect hydrate stability slightly, (2) the changes in both the type and the concentration of cations, which occur in normal diagenetic processes, do not exert a significant influence on the methane hydrate stability conditions, and (3) the shift of hydrate stability in pore water can be expressed as a function of the Cl− concentration only. Based on the results above, an empirical equation ΔT (K)=0.00206 Cl− (mmol/dm3) has been obtained for estimating the shift in the equilibrium temperature of methane hydrate in pore water at a given pressure.  相似文献   

15.
南海北部天然气水合物研究进展   总被引：11，自引：0，他引：11  
天然气水合物是一种新型的储量巨大的绿色能源,是目前世界各国研究界的研究热点之一。我国以及美国、日本、印度、韩国等国家都采集到了天然气水合物的实物样品。虽然我国对天然气水合物的研究起步较晚,但近年来的研究已经取得了飞速的进步,而且也于2007年5月在南海北部陆坡的神狐海域成功采集到天然气水合物的实物样品,这是在南海海域首次获取天然气水合物实物样品,证实了南海北部蕴藏着丰富的天然气水合物资源,标志着我国天然气水合物调查研究水平又上了一个新的台阶。目前,南海北部陆坡已经作为我国天然气水合物未来开发的战略选区之一。在总结我国天然气水合物以往十几年研究工作的基础上,综述了我国天然气水合物近年来在南海北部的地质、地球物理、地球化学3个方面的研究进展,提出了未来天然气水合物勘探和研究的方向和建议。  相似文献   

16.
The physicochemical properties of 21 marine sediment samples were investigated, collected from five different localities along the Jordanian coast of the Gulf of Aqaba. According to the chemical parameters, sediments were categorized into three groups: carbonate (80% CaCO3), composed mainly of materials of calcareous skeletal structures; terrigenous (<10% CaCO3) depositional areas for land-derived materials from surrounding rocks and alluviums; and a admixture of the first two (19–37% CaCO3). High significant linear correlations were found between organic carbon (OC) and total nitrogen (TN), indicating the occurrence of these components in a common phase (organic matter). Despite the co-occurrence of TP in organic matter, these two elements were negatively correlated, indicating anthropogenic sources of pollution such as phosphate exportation (hotel areas and clinker port sites) and industrial activities (industrial complex site). The study found that variations in texture properties and mud contents were due to differences in sediment sources, topography and their response during currents and waves. The finer, well-sorted sediments contain lower elemental concentrations of OC, calcium carbonate and TN (excluding TP) than coarser, poorly-sorted sediments.  相似文献   

17.
Hydro-thermo-chemo and mechanically coupled processes determine hydrate morphology and control gas production from hydrate-bearing sediments. Force balance, together with mass and energy conservation analyses anchored in published data provide robust asymptotic solutions that reflect governing processes in hydrate systems. Results demonstrate that hydrate segregation in clayey sediments results in a two-material system whereby hydrate lenses are surrounded by hydrate-free water-saturated clay. Hydrate saturation can reach ≈2% by concentrating the excess dissolved gas in the pore water and ≈20% from metabolizable carbon. Higher hydrate saturations are often found in natural sediments and imply methane transport by advection or diffusion processes. Hydrate dissociation is a strongly endothermic event; the available latent heat in a reservoir can sustain significant hydrate dissociation without triggering ice formation during depressurization. The volume of hydrate expands 2-to-4 times upon dissociation or CO2CH4 replacement. Volume expansion can be controlled to maintain lenses open and to create new open mode discontinuities that favor gas recovery. Pore size is the most critical sediment parameter for hydrate formation and gas recovery and is controlled by the smallest grains in a sediment. Therefore any characterization must carefully consider the amount of fines and their associated mineralogy.  相似文献   

18.
Authigenic carbonates are frequently associated with methane cold-seep systems, which extensively occur in various geologic settings worldwide. Of interest is the relation between the fluids involved in their formation and the isotopic signals recorded in the carbonate cements. Along the Northern Apennines foothills (Italy), hydrocarbons and connate waters still seeping nowadays are believed to be the primary sources for the formation of fossil authigenic carbonate found in Plio-Pleistocene marine sediments. Four selected outcrops of dolomitic authigenic carbonates were analysed to compare signature of seeping fluids with fractionation of stable carbon and oxygen isotopes recorded in the carbonate.Along the foothills, deep methane-rich fluids spontaneously rise to the surface through mud volcanoes or are exploited in wells drilled nearby to the fossil Plio-Pleistocene authigenic carbonates. The plumbing system providing fluids to present-day cold seeps was structurally achieved in Late Miocene and Plio-Pleistocene. δ13C values of methane, which vary from −51.9 to −43.0‰ VPDB, indicate that gas composition from the deep hydrocarbon reservoirs is relatively uniform along the foothills. On the contrary, δ13C in fossil authigenic carbonates strongly varies among different areas and also within the same outcrop.The different carbon sources that fed the investigated carbonates were identified and include: thermogenic methane from the deep Miocene reservoirs, 13C-enriched CO2 derived from secondary methanogenesis and microbial methane from Pliocene successions buried in the Po Plain. The δ13C variability documented among samples from a single outcrop testifies that the authigenic carbonates might represent a record of varying biogeochemical processes in the hydrocarbon reservoirs. The sources of stable oxygen isotopes in authigenic carbonates are often ascribed to marine water. Oxygen isotopic fractionation in the dolomite cements indicates that marine pore water couldn't be the sole source of oxygen. δ18O values provide a preliminary evidence that connate waters had a role in the carbonates precipitation. The concomitant occurrence of active cold seepages and fossil record of former plumbing systems suggests that generation and migration of hydrocarbons are long-lasting and very effective processes along the Northern Apennines foothills.  相似文献   

19.
用地球化学方法勘查中国南海的天然气水合物   总被引：7，自引：0，他引：7  
天然气水合物是一种未来新型能源,赋存于低温高压环境下的海洋沉积物中,但也可形成于大陆永久冻土带中。天然气水合物资源量巨大,具有经济和环境上的研究意义。近年来,国际上己对天然气水合物的产况、分布和形成机理开展了大量研究,但国内这方面的工作还刚刚开展。对中国南海的调查表明该区存在天然气水合物赋存的有利地质条件、温压条件和富含有机质的沉积条件。在南海的许多海区还发现了指示天然气水合物存在的地震标志(BSR)。介绍了在南海天然气水合物勘查中的地球化学异常标志。这些地球化学异常的产生可能与天然气水合物的形成或分解过程有关。研究内容包括沉积物中气体含量(主要为甲烷和乙烷),甲烷的碳同位素,孔隙水中阴离子(Cl^-、SO4^2-等)、阳离子(Ca^2 、Mg^2 、Ba^2 、Sr^2 ,B^3 和NH4^ 等)浓度和δ^18,δD,δ^11B,及^87Sr／^86Sr等同位素组成,此外还对海底沉积物的热释光特征和紫外、可见、近红外反射光谱特征开展了探索性研究。通过进一步加强理论和实验研究,结合地球物理和地球化学资料,在不远的将来将会在南海发现和圈定天然气水合物矿藏。  相似文献   

20.
运用实验模拟的手段,对铀(U)、钍(Th)在碳酸钙-海水界面的附着行为进行了初步研究,通过测定相关的分异系数(D)定量评估了文石和方解石两种碳酸钙矿物对U和Th的捕集作用。实验结果显示,不仅U和Th之间存在显著差异,而且两种碳酸钙矿物之间也存在明显不同。U介于碳酸钙和海水之间的分异系数(DU)分别在1.5~3.5(文石)和0.04~0.19(方解石)区间内变化,分异行为非常微弱但其分异系数随着碳酸钙沉淀速率的增加而逐渐上升。这表明U元素主要是以共沉淀的方式进入到文石或方解石沉淀中,但由于其在海水溶液中主要以2 22 3UO(CO)nn的形式存在,因而只能以占据晶格缺陷的方式进入碳酸钙。与之相反的是,文石和方解石都对Th表现出极强的捕集能力,所测定的分异系数(DTh)分别在240~6 330(文石)和430~6 160(方解石)范围内变化,但DTh与碳酸钙沉淀速率之间无明显关联。Th在碳酸钙表面的附着行为可界定为单纯的吸附作用,这一行为应与Th主要以Th(OH)4的形式赋存于溶液中有关。  相似文献   

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