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Gas hydrates in shallow deposits of the Amsterdam mud volcano, Anaximander Mountains, Northeastern Mediterranean Sea

机译:阿姆斯特丹泥火山,Anaximander山,东北地中海的浅层沉积物中的天然气水合物

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摘要

We investigated gas hydrate in situ inventories as well as the composition and principal transport mechanisms of fluids expelled at the Amsterdam mud volcano (AMV; 2,025 m water depth) in the Eastern Mediterranean Sea. Pressure coring (the only technique preventing hydrates from decomposition during recovery) was used for the quantification of light hydrocarbons in near-surface deposits. The cores (up to 2.5 m in length) were retrieved with an autoclave piston corer, and served for analyses of gas quantities and compositions, and pore-water chemistry. For comparison, gravity cores from sites at the summit and beyond the AMV were analyzed. A prevalence of thermogenic light hydrocarbons was inferred from average C1/C2+ ratios <35 and δ13C-CH4 values of 50.6‰. Gas venting from the seafloor indicated methane oversaturation, and volumetric gas–sediment ratios of up to 17.0 in pressure cores taken from the center demonstrated hydrate presence at the time of sampling. Relative enrichments in ethane, propane, and iso-butane in gas released from pressure cores, and from an intact hydrate piece compared to venting gas suggest incipient crystallization of hydrate structure II (sII). Nonetheless, the co-existence of sI hydrate can not be excluded from our dataset. Hydrates fill up to 16.7% of pore volume within the sediment interval between the base of the sulfate zone and the maximum sampling depth at the summit. The concave-down shapes of pore-water concentration profiles recorded in the center indicate the influence of upward-directed advection of low-salinity fluids/fluidized mud. Furthermore, the SO4 2 and Ba2+ pore-water profiles in the central part of the AMV demonstrate that sulfate reduction driven by the anaerobic oxidation of methane is complete at depths between 30 cm and 70 cm below seafloor. Our results indicate that methane oversaturation, high hydrostatic pressure, and elevated pore-water activity caused by low salinity promote fixing of considerable proportions of light hydrocarbons in shallow hydrates even at the summit of the AMV, and possibly also of other MVs in the region. Depending on their crystallographic structure, however, hydrates will already decompose and release hydrocarbon masses if sediment temperatures exceed ca. 19.3°C and 21.0°C, respectively. Based on observations from other mud volcanoes, the common occurrence of such temperatures induced by heat flux from below into the immediate subsurface appears likely for the AMV.
机译:我们调查了天然气水合物的原位清单,以及在东地中海阿姆斯特丹泥火山(AMV; 2,025 m水深)处驱出的流体的组成和主要传输机制。压力取芯(防止水合物在回收过程中分解的唯一技术)用于量化近地表沉积物中的轻烃。用高压釜活塞式取芯器取回岩心(长度最大为2.5 m),并用于分析气体数量和成分以及孔隙水化学。为了进行比较,分析了山顶和AMV以外站点的重力核心。从平均C1 / C2 +比率<35和δ13C-CH4值为50.6‰推断出产热轻烃的患病率。从海底排出的气体表明甲烷过饱和,从中心抽出的压力岩心中气体与沉积物的体积比高达17.0,表明在取样时存在水合物。与排出的气体相比,压力岩心和完整的水合物块中释放的气体中乙烷,丙烷和异丁烷的相对富集表明水合物结构II(sII)的初期结晶。但是,不能从我们的数据集中排除sI水合物的共存。在硫酸盐带底部与顶峰最大采样深度之间的沉积物间隔内,水合物最多可填满孔隙体积的16.7%。中心记录的孔隙水浓度分布曲线的下凹形状表明了低盐度流体/流化泥浆的向上对流的影响。此外,AMV中心部分的SO4 2和Ba2 +孔隙水剖面表明,由甲烷的厌氧氧化驱动的硫酸盐还原在海床以下30 cm至70 cm的深度处完成。我们的结果表明,低盐度引起的甲烷过饱和,高静水压力和较高的孔隙水活度,即使在AMV的顶峰,也可能在该地区的其他MV上,都可以固定浅水合物中相当比例的轻烃。但是,取决于沉积物的晶体结构,如果沉积物温度超过约200℃,则水合物已经分解并释放出烃类物质。分别为19.3°C和21.0°C。根据来自其他泥火山的观察,AMV可能会发生由下而下直接进入地下的热通量引起的这种温度的普遍发生。

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