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海底天然气水合物藏是天然的巨型碳储藏库,是深部甲烷等烃类气体运移至海底过程中暂时的碳储,是地球碳循环过程的重要一环。冷泉通常与海底天然气水合物藏分解密切相关,是深源或浅层气及水合物分解气在海底发生渗漏的现象。该文根据国内外天然气水合物及冷泉系统勘查的最新动向,综述了与水合物及冷泉流体渗漏相关的羽状流、运移通道、海底微地形地貌等要素的海底原位观测技术,主要包括：走航式及坐底式原位观测、海面及低空渗漏甲烷观测、海底可视化观测、与水合物及冷泉相关的海底观测网络等。综合使用原位观测技术可以更细致、全面地描绘水合物和冷泉系统的时空“景象”,更好地协助厘清海底渗漏甲烷的归趋,拓展人类对深海独特生命绿洲的认知。 相似文献
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为了准确理解冷泉水体中甲烷气体的分布规律,综合运用单波束测深数据和冷泉水体流场数据,建立了冷泉气泡上升、溶解速率的定量反演方法,利用现场海试资料对反演方法进行了验证,并对海试区域的冷泉气体溢出、溶解通量以及冷泉水体的甲烷浓度进行了估算。计算结果表明,考察船航向与冷泉水体流向的差异会对声学探测结果产生影响,当航向与流向的夹角大于±60°时,声学成像中冷泉倾角的误差将超过50%。同时,冷泉气泡上升速率的衰减与溢出口水深显著相关,相关系数可达0.9,并且冷泉上升流对上升速率的提升效果明显。水合物稳定带的分布对冷泉气泡的收缩速率影响显著,稳定带内、外收缩速率的差异可达3～4倍。冷泉气体通量的计算结果表明,调查区域内冷泉的溢出强度整体较大,同时溶解通量与水深之间呈现明显的分段效应。根据冷泉气体溶解通量估算的冷泉水体甲烷浓度与色谱分析结果具有较好的一致性。相关研究有助于实现对冷泉水体中甲烷气体分布的定量评估,为潜在海底冷泉区的圈划和海域天然气水合物的调查提供技术支撑。 相似文献
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截然不同的3个天然气水合物区域通过海底的CH4通量:对大洋和大洋化学的影响 总被引：1，自引：0，他引：1
在全球甲烷储库中甲烷水合物的作用缺乏充分的评估,因为人们对甲烷通过海底表面进入大洋和大气过程中的搬运以及在水柱中作为营养剂消耗的程度所知甚少。在3个截然不同的气体水合物环境中,在甲烷羽中或其附近采集孔隙流体和水柱样品,分析甲烷、溶解有机碳（DIC）、硫化物/硫酸盐、 相似文献
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海底冷泉多由海底天然气渗漏形成,是以水、碳氢化合物、硫化氢或二氧化碳为主要成分的流体.它既是海底天然气水合物存在的标志,又与温室效应、海洋生态环境、冷泉生物群落等问题密切相关,对海底冷泉的流体渗漏通量和化学组成进行测定,对认识上述问题有重大意义.与实验室化学分析和数值模拟相比,原位观测可保证数据的可靠性和真实性,作为冷... 相似文献
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浅成天然气水合物呈致密块状赋存在海床面上或海床附近,在全球大陆坡上有广范的分布,由于其饱和度高及赋存部位浅因而被认为更适于开采。与甲烷渗漏、气体烟囱和水合物丘密切相伴的浅成天然气水合物,是在构造活动带由高通量的富甲烷流体以集束方式沿断层或断裂破碎带上升形成的。推测在我国南海北坡也可能存在浅成天然气水合物。 相似文献
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天然气水合物赋存在极地的广义地区,通常与近岸和近海的冻土层以及大陆和岛屿外缘的沉积物相伴生。气体水合物中甲烷所含碳量可能超过１０＾１９克。气体水合物在三个方面尤为重要,即：化石燃料储藏潜能,海底地质灾害以及对全球气候变化的影响,由于气体水合物代表地球表层２０００ｍ范围内的大量甲烷,故将其作为一种非常规的、未查验的化石燃料来源,因为气体水合物处于亚稳定状态,故温压变化影响其稳定性,海底之下未稳定的气 相似文献
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对日本海西部大陆坡沉积物柱状样中的自生碳酸盐样品进行了X射线衍射、扫描电镜、地球化学和碳氧同位素组成的系统研究。X射线衍射和扫描电镜分析结果表明,碳酸盐主要组成矿物为颗粒状自生高镁方解石微晶,放射状自生文石微晶仅在一个层位出现。结合碳酸盐的地球化学组成,认为研究区碳酸盐来自于富Ca2+、Mg2+和HCO3-流体的沉淀。中度亏损的13C(-33.85‰～-39.53‰)表明碳来自于甲烷的厌氧氧化,同时,这也是研究区海底存在甲烷冷泉的重要证据。重氧同位素比值(5.28‰～5.31‰)则指示着富18O流体来源,而该流体应源于天然气水合物的分解。综上可知,研究区碳酸盐来自于研究区甲烷冷泉上升流的沉淀,指示着海底更深处天然气水合物的存在与分解。 相似文献
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海洋孔隙水的硫酸盐剖面在底层气体水合物甲烷通量中的指示ＷａｌｔｅｒＳ．Ｂｏｒｏｗｓｋｉ等微生物硫酸盐的减少，微生物沼气的产量，和气体水合物的形成与深海、大陆边缘沉积物中出现的成岩作用紧密联系（Ｐａｕｌｌ等，１９９４）．气体水合物是由水和低分子量气体（... 相似文献
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天然气水合物是一种类似冰状的结晶固体,晶体中烃和非烃气体被水分子的刚性构架所封存。因为是由细菌的甲烷水合物（结构Ⅰ）和复杂的热成天然气水合物（结构Ⅱ和Ｈ）二者构成,所以墨西哥湾陆坡的天然气水合物在全球环境中是非常典型的。结构Ⅱ水合物和结构Ｈ水合物含有... 相似文献
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Soil-sized particulates have been collected on board ship by a mesh technique from the lower troposphere of the North, Equatorial and South Atlantic Ocean, northern and southern Indian Ocean, South and East China Sea and various coastal localities.Spectrographic analysis reveals that, on average, the particulates have concentrations of Mn, Ni, Co, Ga, Cr, V, Ba, and Sr which are of the same order of magnitude as those in average crustal material. In contrast, the average concentrations of Pb, Sn, and Zn are one order of magnitude higher than those in average crustal material.Within this “world-wide” average there are significant geographical variations in the distributions of Pb, Sn, and Zn which may be related to anthropogenic sources.On the basis of trace-element distributions lower tropospheric soil-sized marine particulates have been divided into four genetic components; local, zonal, inter-zonal, and global. The proportions of these components vary geographically, and each component may have both a natural and an anthropogenic fraction. 相似文献
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Tautog, Tautoga onitis, is an abundant species of fish in estuaries of the northeastern United States. Planktonic tautog larvae are abundant in summer in these estuaries, but there is little information on rates of growth of tautog larvae feeding on natural assemblages of food in the plankton. We examined abundance and growth of larval tautog and environmental factors during weekly sampling at three sites along a nearshore‐to‐offshore transect in Buzzards Bay, Massachusetts, USA during summer 1994. This is the first study of a robust sample size (336 larvae) to estimate growth rates of field‐caught planktonic tautog larvae feeding on natural diets, using the otolith daily‐growth‐increment method. The study was over the entire summer period when tautog larvae were in the plankton. The sampling sites contrasted in several environmental variables including temperature, dissolved oxygen (DO), and chlorophyll a concentration. There was a temporal progression in the abundance of tautog larvae over the summer, in relation to location and temperature. Tautog larvae were first present nearshore, with a pronounced peak in abundance occurring at the nearshore sites during the last 2 weeks in June. Larvae were absent at this time further offshore. From late June through August, larval abundance progressively decreased nearshore, but increased offshore although never approaching the abundance levels observed at the nearshore sites. The distribution and abundance of tautog larvae appeared to be related to a nearshore‐to‐offshore seasonal warming trend and a nearshore decrease in DO. Otoliths from 336 larvae ranging from 2.3 to 7.7 mm standard length had otolith increment counts ranging from 0 to 19 increments. Growth of larval tautog was estimated at 0.23 mm·day?1, and length of larvae prior to first increment formation was estimated at 2.8 mm indicating that first increment formation occurs 3–4 days after hatching at 2.2 mm. Despite spatial and temporal differences in environmental factors, there were no significant differences in growth rates at any of three given sites over time, or between sites. Because larval presence only occurred at a narrow range of temperature (17–23.5 °C) and DO (6.5–9.3 mg·l?1), in situ differences in growth did not appear to be because of differences in larval distribution and abundance patterns relative to these parameters. 相似文献
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Lars-Göran Danielsson 《Marine Chemistry》1980,8(3):199-215
Results of trace-metal analyses of water samples obtained during a cruise with the Soviet R.V. “Akademik Kurchatov” in the Indian Ocean are presented. The determinations were performed on board with atomic absorption spectrophotometry after a two-stage dithiocarbamate—Freon extraction procedure. Trace-metal concentrations found are in the same range as those found recently for similar open-ocean areas by other workers. The values for lead and zinc are probably high due to contamination. Vertical profiles indicate biogenic processes as controlling factors for the increase of cadmium, copper and nickel concentrations with depth. Iron shows an irregular depth distribution as a result of large random variations in concentration. 相似文献
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Klaus Kremling 《Marine Chemistry》1983,13(2):87-108
In June 1981, dissolved Zn, Cd, Cu, Ni, Co, Fe, and Mn were determined from two detailed profiles in anoxic Baltic waters (with extra data for Fe and Mn from August 1979). Dramatic changes across the O2H2S interface occur in the abundances of Cu, Co, Fe, and Mn (by factors of ?100). The concentrations of Zn, Cd, and Ni at the redox front decrease by factors between 3 to 5.Equilibrium calculations are presented for varying concentrations of hydrogen sulfide and compared with the field data. The study strongly supports the assumption that the solubility of Zn, Cd, Cu, and Ni is greatly enhanced and controlled by the formation of bisulfide and(or) polysulfide complexes. Differences between predicted and measured concentrations of these elements are mainly evident at lower ΣH2S concentrations.Cobalt proved to be very mobile in anoxic regions, and the results indicate that the concentrations are limited by CoS precipitation. The iron (Fe2+) and manganese (Mn2+) distribution in sulfide-containing waters is controlled by total flux from sediment-water interfaces rather than by equilibrium concentrations of their solid phases (FeS and MnCO3). The concentrations of these metals are therefore expected to increase with prolonged stagnation periods in the basin. 相似文献
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P.N. Froelich L.W. Kaul J.T. Byrd M.O. Andreae K.K. Roe 《Estuarine, Coastal and Shelf Science》1985,20(3):239-264
Concentrations of dissolved nutrients (NO3, PO4, Si), germanium species, arsenic species, tin, barium, dimethylsulfide and related parameters were measured along the salinity gradient in Charlotte Harbor. Phosphate enrichment from the phosphate industry on the Peace River promotes a productive diatom bloom near the river mouth where NO3 and Si are completely consumed. Inorganic germanium is completely depleted in this bloom by uptake into biogenic opal. The ratio taken up by diatoms is about 0·7 × 10?6, the same as that provided by the river flux, confirming that siliceous organisms incorporate germanium as an accidental trace replacement for silica. Monomethylgermanium and dimethylgermanium concentrations are undetectable in the Peace River, and increase linearly with increasing salinity to the seawater end of the bay, suggesting that these organogermanium species behave conservatively in estuaries, and are neither produced nor consumed during estuarine biogenic opal formation or dissolution. Inorganic arsenic displays slight removal in the bloom. Monomethylarsenic is produced both in the bloom and in mid-estuary, while dimethylarsenic is conservative in the bloom but produced in mid-estuary. The total production of methylarsenicals within the bay approximately balances the removal of inorganic arsenic, suggesting that most biological arsenic uptake in the estuary is biomethylated and released to the water column. Dimethylsulfide increases with increasing salinity in the estuary and shows evidence of removal, probably both by degassing and by microbial consumption. An input of DMS is observed in the central estuary. The behavior of total dissolvable tin shows no biological activity in the bloom or in mid-estuary, but does display a low-salinity input signal that parallels dissolved organic material, perhaps suggesting an association between tin and DOM. Barium displays dramatic input behavior at mid-salinities, probably due to slow release from clays deposited in the harbor after catastrophic phosphate slime spills into the Peace River. 相似文献